<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ashebir, Mengstu Etay</style></author><author><style face="normal" font="default" size="100%">Sabhapathy, Palani</style></author><author><style face="normal" font="default" size="100%">Nasr, Osama</style></author><author><style face="normal" font="default" size="100%">Modak, Varad</style></author><author><style face="normal" font="default" size="100%">Moradlou, Omran</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Huang,Chih-Yang</style></author><author><style face="normal" font="default" size="100%">Nachimuthu, Santhanamoorthi</style></author><author><style face="normal" font="default" size="100%">Jiang, Jyh-Chiang</style></author><author><style face="normal" font="default" size="100%">Hu, Ying-Li</style></author><author><style face="normal" font="default" size="100%">Hung, Chen-Hsiung</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Electronic structure engineering of nickel single-atom catalyst by phosphorous for efficient electrocatalytic CO2 reduction reaction in a proton-rich microenvironment</style></title></titles><keywords><keyword><style  face="normal" font="default" size="100%">ELECTRONIC STRUCTURE</style></keyword><keyword><style  face="normal" font="default" size="100%">Electroreduction</style></keyword><keyword><style  face="normal" font="default" size="100%">Proton microenvironment</style></keyword><keyword><style  face="normal" font="default" size="100%">Single atom</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2025</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S1385894725021400</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">509</style></volume><pages><style face="normal" font="default" size="100%">161319</style></pages><isbn><style face="normal" font="default" size="100%">1385-8947</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The electrocatalytic carbon dioxide reduction reaction (eCO2RR) in an acidic environment is crucial for mitigating carbonate and bicarbonate formation while enhancing CO2 conversion efficiency. However, the hydrogen evolution reaction (HER) often outcompetes eCO2RR in a proton-rich microenvironment, posing a significant challenge. This study introduces an in-situ phosphatizing method to alter the electronic structure of a Ni–N4 single-atom catalyst (Ni–N3PC), thereby suppressing HER and promoting eCO2RR performance in acidic environments. The Ni–N3PC catalyst achieves a CO Faradaic efficiency (FE) exceeding 90 % over a wide potential range, high carbon conversion efficiency, a CO partial current density of –357.7 mA cm−2, and long-term stability for 100 h at –100 mA cm−2 with a FE of 85 %. Electrochemical impedance spectroscopy and turnover frequency analysis reveal that Ni–N3PC exhibits lower charge-transfer resistance and higher intrinsic activity, respectively. The structural characterization using X-ray absorption spectroscopy confirms the formation of Ni–P and Ni–N bonds while scanning transmission electron microscopy shows atomically dispersed Ni atoms on carbon networks. Density functional theory calculations further support the experimental results, showing that Ni–N3PC significantly lowers the energy barrier for the key *COOH intermediate, resulting in outstanding eCO2RR performance. This research provides valuable insights into the design of highly efficient Ni single-atom catalysts for industrial eCO2RR applications.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Yusuf Fakhri, Muhammad</style></author><author><style face="normal" font="default" size="100%">Lai, Wei-Ching</style></author><author><style face="normal" font="default" size="100%">Jarwal, Bhawna</style></author><author><style face="normal" font="default" size="100%">Hsieh, Wan-Zhen</style></author><author><style face="normal" font="default" size="100%">Tseng, Yu-Hsiang</style></author><author><style face="normal" font="default" size="100%">Ho, Thi-Thong</style></author><author><style face="normal" font="default" size="100%">Bayikadi, Khasim Saheb</style></author><author><style face="normal" font="default" size="100%">Valiyaveettil, Suneesh M.</style></author><author><style face="normal" font="default" size="100%">Ganesan, Peramiyan</style></author><author><style face="normal" font="default" size="100%">Chiang, Ching-Yu</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhanced low-temperature thermoelectric properties in textured polycrystalline SnS Co-doped with Na and Ag</style></title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Co-doping</style></keyword><keyword><style  face="normal" font="default" size="100%">Electrical transport properties</style></keyword><keyword><style  face="normal" font="default" size="100%">Polycrystalline SnS</style></keyword><keyword><style  face="normal" font="default" size="100%">Sintering</style></keyword><keyword><style  face="normal" font="default" size="100%">Texture modulation</style></keyword><keyword><style  face="normal" font="default" size="100%">Thermoelectric properties</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2025</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0925838825006826</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">1018</style></volume><pages><style face="normal" font="default" size="100%">179124</style></pages><isbn><style face="normal" font="default" size="100%">0925-8388</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Tin monosulfide (SnS), an affordable group IV-VI binary compound, has emerged as a promising semiconductor due to its abundance and low toxicity. The exceptionally low thermal conductivity from the strong lattice anharmonicity makes this material suitable for thermoelectric applications. However, the poor thermoelectric properties of polycrystalline, compared to its single-crystal counterpart, remain the challenge. Furthermore, the anisotropic performance based on the sintering process complicates the preparation of this polycrystalline material. In this study, we successfully improved the electrical transport properties of polycrystalline SnS by employing the in-plane transport properties with texture modulation from hot-pressing at 973 K. This enhancement led to the high electrical conductivity of ≈ 55 S cm−1 in polycrystalline Na-doped SnS observed at room temperature. Additionally, the hole carrier concentration of p-type SnS was further optimized by co-doping of Na and Ag. Our co-doped SnS exhibits a relatively high power factor peak of ≈ 4.49 μWcm−1K−2 at 473 K. With the significant improvement of the electrical conductivities, the thermal conductivities remained unaltered. This work successfully demonstrated a substantial enhancement by ∼66.7 % in the thermoelectric figure of merit (zT) from 0.18 to 0.3 at a relatively low temperature of 573 K in polycrystalline SnS via the microstructural modification from texturing and the optimization of carrier concentration from co-doping.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Thang, Nguyen Quoc</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Putikam, Raghunath</style></author><author><style face="normal" font="default" size="100%">Huang,Chih-Yang</style></author><author><style face="normal" font="default" size="100%">Lin, Tsai-Yu</style></author><author><style face="normal" font="default" size="100%">Kamal Hussien, Mahmoud</style></author><author><style face="normal" font="default" size="100%">Heng-Liang Wu</style></author><author><style face="normal" font="default" size="100%">Lin, Ming-Chang</style></author><author><style face="normal" font="default" size="100%">Chih-Hao Lee</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Regulating COOH Intermediate via Rationally Constructed Surface-Active Sites of Bi2WO6 for Solar-Driven CO2-to-CO Production</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Functional Materials</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">active sites</style></keyword><keyword><style  face="normal" font="default" size="100%">COOH</style></keyword><keyword><style  face="normal" font="default" size="100%">Ni single atoms</style></keyword><keyword><style  face="normal" font="default" size="100%">oxygen vacancies</style></keyword><keyword><style  face="normal" font="default" size="100%">surface reaction</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2025</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/adfm.202423751</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><volume><style face="normal" font="default" size="100%">n/a</style></volume><pages><style face="normal" font="default" size="100%">2423751</style></pages><isbn><style face="normal" font="default" size="100%">1616-301X</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Abstract Solar-driven CO2 reduction holds great promise for sustainable energy, yet the role of atomic active sites in governing intermediate formation and conversion remains poorly understood. Herein, a synergistic strategy using Ni single atoms (SAs) and surface oxygen vacancies (Ov) is reported to regulate the CO2 reduction pathway on the Bi2WO6 photocatalyst. Combining in-situ techniques and theoretical modeling, the reaction mechanism and the structure-activity relationship is elucidated. In-situ X-ray absorption spectroscopy identifies Bi and Ni as active sites, and in-situ diffuse reflectance infrared Fourier transform spectroscopy demonstrates that adsorption of H2O and CO2 readily forms CO32? species on the Ov-rich catalyst. Optimally balancing Ni SAs and Ov lowers the energy barrier for the formation and dehydration of a key COOH intermediate, leading to favorable CO formation and desorption. Consequently, a superior CO production efficiency of 53.49 µmol g?1 is achieved, surpassing previous reports on Bi2WO6-based catalysts for gas-phase CO2 photoreduction.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">n/a</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Thang, Nguyen Quoc</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">et al</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Back cover</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2024</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D4TA90226B</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">32483 - 32484</style></pages><isbn><style face="normal" font="default" size="100%">2050-7488</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><issue><style face="normal" font="default" size="100%">46</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jarwal, Bhawna</style></author><author><style face="normal" font="default" size="100%">Suman Abbas</style></author><author><style face="normal" font="default" size="100%">Chou, Ta-Lei</style></author><author><style face="normal" font="default" size="100%">Vailyaveettil, Suneesh M.</style></author><author><style face="normal" font="default" size="100%">Kumar, Ashutosh</style></author><author><style face="normal" font="default" size="100%">Quadir, Shaham</style></author><author><style face="normal" font="default" size="100%">Ho, Thi-Thong</style></author><author><style face="normal" font="default" size="100%">Deniz P. Wong</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Boosting Thermoelectric Performance in Nanocrystalline Ternary Skutterudite Thin Films through Metallic CoTe2 Integration</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; InterfacesACS Applied Materials &amp; Interfaces</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2024</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acsami.3c17695</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">14770 - 14780</style></pages><isbn><style face="normal" font="default" size="100%">1944-8244</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">n/a</style></abstract><issue><style face="normal" font="default" size="100%">12</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;doi: 10.1021/acsami.3c17695&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kamal Hussien, Mahmoud</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Mohammad Qorbani</style></author><author><style face="normal" font="default" size="100%">Putikam, Raghunath</style></author><author><style face="normal" font="default" size="100%">Kholimatussadiah, Septia</style></author><author><style face="normal" font="default" size="100%">Tzou, Der-Lii M.</style></author><author><style face="normal" font="default" size="100%">Hammad Elsayed, Mohamed</style></author><author><style face="normal" font="default" size="100%">Lu, Yu-Jung</style></author><author><style face="normal" font="default" size="100%">Wang, Yen-Yu</style></author><author><style face="normal" font="default" size="100%">Lee, Xing-Hao</style></author><author><style face="normal" font="default" size="100%">Lin, Tsai-Yu</style></author><author><style face="normal" font="default" size="100%">Thang, Nguyen Quoc</style></author><author><style face="normal" font="default" size="100%">Heng-Liang Wu</style></author><author><style face="normal" font="default" size="100%">Haw, Shu-Chih</style></author><author><style face="normal" font="default" size="100%">Wu, Kevin C.-W.</style></author><author><style face="normal" font="default" size="100%">Lin, Ming-Chang</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Constructing B─N─P Bonds in Ultrathin Holey g-C3N4 for Regulating the Local Chemical Environment in Photocatalytic CO2 Reduction to CO</style></title><secondary-title><style face="normal" font="default" size="100%">Small</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">CO2 reduction</style></keyword><keyword><style  face="normal" font="default" size="100%">Exciton dissociation</style></keyword><keyword><style  face="normal" font="default" size="100%">Graphitic carbon nitride</style></keyword><keyword><style  face="normal" font="default" size="100%">metal-free</style></keyword><keyword><style  face="normal" font="default" size="100%">Photocatalysis</style></keyword><keyword><style  face="normal" font="default" size="100%">reaction mechanism</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2024</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/smll.202400724</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><volume><style face="normal" font="default" size="100%">n/a</style></volume><pages><style face="normal" font="default" size="100%">2400724</style></pages><isbn><style face="normal" font="default" size="100%">1613-6810</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Abstract The lack of intrinsic active sites for photocatalytic CO2 reduction reaction (CO2RR) and fast recombination rate of charge carriers are the main obstacles to achieving high photocatalytic activity. In this work, a novel phosphorus and boron binary-doped graphitic carbon nitride, highly porous material that exhibits powerful photocatalytic CO2 reduction activity, specifically toward selective CO generation, is disclosed. The coexistence of Lewis-acidic and Lewis-basic sites plays a key role in tuning the electronic structure, promoting charge distribution, extending light-harvesting ability, and promoting dissociation of excitons into active carriers. Porosity and dual dopants create local chemical environments that activate the pyridinic nitrogen atom between the phosphorus and boron atoms on the exposed surface, enabling it to function as an active site for CO2RR. The P?N?B triad is found to lower the activation barrier for reduction of CO2 by stabilizing the COOH reaction intermediate and altering the rate-determining step. As a result, CO yield increased to 22.45 µmol g?1 h?1 under visible light irradiation, which is ≈12 times larger than that of pristine graphitic carbon nitride. This study provides insights into the mechanism of charge carrier dynamics and active site determination, contributing to the understanding of the photocatalytic CO2RR mechanism.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">n/a</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Krishnamoorthy, Vimal</style></author><author><style face="normal" font="default" size="100%">Bangolla, Hemanth K.</style></author><author><style face="normal" font="default" size="100%">Chen, Chi-Yang</style></author><author><style face="normal" font="default" size="100%">Huang, Yu-Ting</style></author><author><style face="normal" font="default" size="100%">Cheng, Cheng-Maw</style></author><author><style face="normal" font="default" size="100%">Ulaganathan, Rajesh K.</style></author><author><style face="normal" font="default" size="100%">Raman Sankar</style></author><author><style face="normal" font="default" size="100%">Lee, Kuei-Yi</style></author><author><style face="normal" font="default" size="100%">He-Yun Du</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Chen, Kuei-Hsieh</style></author><author><style face="normal" font="default" size="100%">Ruei-San Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Efficient Hydrogen Evolution Reaction in 2H-MoS2 Basal Planes Enhanced by Surface Electron Accumulation</style></title><secondary-title><style face="normal" font="default" size="100%">Catalysts</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">hydrogen evolution reaction</style></keyword><keyword><style  face="normal" font="default" size="100%">molybdenum disulfide</style></keyword><keyword><style  face="normal" font="default" size="100%">overpotential</style></keyword><keyword><style  face="normal" font="default" size="100%">surface electron accumulation</style></keyword><keyword><style  face="normal" font="default" size="100%">Tafel slope</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><isbn><style face="normal" font="default" size="100%">2073-4344</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;An innovative strategy has been developed to activate the basal planes in molybdenum disulfide (MoS2) to improve their electrocatalytic activity by controlling surface electron accumulation (SEA) through aging, annealing, and nitrogen-plasma treatments. The optimal hydrogen evolution reaction (HER) performance was obtained on the surface treated with nitrogen-plasma for 120 s. An overpotential of 0.20 V and a Tafel slope of 120 mV dec−1 were achieved for the optimized condition. The angle-resolved photoemission spectroscopy measurement confirmed the HER efficiency enhanced by the SEA conjugated with the sulfur vacancy active sites in the MoS2 basal planes. This study provides new insight into optimizing MoS2 catalysts for energy applications.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mamo, Tadios Tesfaye</style></author><author><style face="normal" font="default" size="100%">Mohammad Qorbani</style></author><author><style face="normal" font="default" size="100%">Hailemariam, Adane Gebresilassie</style></author><author><style face="normal" font="default" size="100%">Putikam, Raghunath</style></author><author><style face="normal" font="default" size="100%">Chu, Che-Men</style></author><author><style face="normal" font="default" size="100%">Ko, Ting-Rong</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Huang,Chih-Yang</style></author><author><style face="normal" font="default" size="100%">Kholimatussadiah, Septia</style></author><author><style face="normal" font="default" size="100%">Tadesse Billo</style></author><author><style face="normal" font="default" size="100%">Kamal Hussien, Mahmoud</style></author><author><style face="normal" font="default" size="100%">Chang, Shuo-Yun</style></author><author><style face="normal" font="default" size="100%">Lin, Ming-Chang</style></author><author><style face="normal" font="default" size="100%">Woon, Wei-Yen</style></author><author><style face="normal" font="default" size="100%">Heng-Liang Wu</style></author><author><style face="normal" font="default" size="100%">Ken-Tsung Wong</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhanced CO2 photoreduction to CH4 via *COOH and *CHO intermediates stabilization by synergistic effect of implanted P and S vacancy in thin-film SnS2</style></title></titles><keywords><keyword><style  face="normal" font="default" size="100%">In situ FTIR</style></keyword><keyword><style  face="normal" font="default" size="100%">In situ NAP-XPS</style></keyword><keyword><style  face="normal" font="default" size="100%">Ion implantation</style></keyword><keyword><style  face="normal" font="default" size="100%">Photocatalysis</style></keyword><keyword><style  face="normal" font="default" size="100%">REACTION PATHWAY</style></keyword><keyword><style  face="normal" font="default" size="100%">Thin film</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2024</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S2211285524006116</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">128</style></volume><pages><style face="normal" font="default" size="100%">109863</style></pages><isbn><style face="normal" font="default" size="100%">2211-2855</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Reduction of CO2 to value-added hydrocarbons through artificial photosynthesis is one of the way to address the energy crisis and climate change issues. It is known that lowering the activation energy of CO2 molecules on the photocatalyst surface and key intermediates is crucial in photocatalytic CO2 reduction. Herein, we present phosphorus-implanted 20-nm SnS2 continuous thin film with sulfur vacancies (i.e., SV-SnS2:P where P substitutes on S sites). The fabrication process involves thermal evaporation, post-sulfurization, and ion implantation. Our gas-phase photocatalytic experiments show an enhanced and selective CO2 photoreduction to CH4 with a yield of 0.13 µmol cm−2 and selectivity of 92 % under solar-light irradiation for 4 h over an optimal ∼4.5 % P and ∼16 % SV. Experimental observations, conducted through X-ray absorption near edge, in situ near ambient pressure X-ray photoelectron, and in situ Fourier transform infrared spectroscopies, along with first-principle density functional theory calculations. Results reveal that P dopant is significantly affected by nearby SV via local charge density transfer from P to the nearest Sn and next-nearest S neighbor atoms, consequently, leads to the stabilization of *COOH and *CHO intermediates, where asterisks stand for P as the active site. Our results demonstrate how active site modulation, without using precious co-catalysts, plays a crucial role in intermediate stabilization in a wireless photocatalysis process.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mohammad Qorbani</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hybrid and Asymmetric Supercapacitors: Achieving Balanced Stored Charge across Electrode Materials</style></title><secondary-title><style face="normal" font="default" size="100%">Small</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">charge balancing</style></keyword><keyword><style  face="normal" font="default" size="100%">charge–discharge current density</style></keyword><keyword><style  face="normal" font="default" size="100%">electrochemical capacitor</style></keyword><keyword><style  face="normal" font="default" size="100%">hybrid and asymmetric device</style></keyword><keyword><style  face="normal" font="default" size="100%">rate capability</style></keyword><keyword><style  face="normal" font="default" size="100%">SUPERCAPACITOR</style></keyword><keyword><style  face="normal" font="default" size="100%">sweep rate</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2024</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/smll.202400558</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><volume><style face="normal" font="default" size="100%">n/a</style></volume><pages><style face="normal" font="default" size="100%">2400558</style></pages><isbn><style face="normal" font="default" size="100%">1613-6810</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Abstract An electrochemical capacitor configuration extends its operational potential window by leveraging diverse charge storage mechanisms on the positive and negative electrodes. Beyond harnessing capacitive, pseudocapacitive, or Faradaic energy storage mechanisms and enhancing electrochemical performance at high rates, achieving a balance of stored charge across electrodes poses a significant challenge over a wide range of charge?discharge currents or sweep rates. Consequently, fabricating hybrid and asymmetric supercapacitors demands precise electrochemical evaluations of electrode materials and the development of a reliable methodology. This work provides an overview of fundamental aspects related to charge-storage mechanisms and electrochemical methods, aiming to discern the contribution of each process. Subsequently, the electrochemical properties, including the working potential windows, rate capability profiles, and stabilities, of various families of electrode materials are explored. It is then demonstrated, how charge balancing between electrodes falters across a broad range of charge?discharge currents or sweep rates. Finally, a methodology for achieving charge balance in hybrid and asymmetric supercapacitors is proposed, outlining multiple conditions dependent on loaded mass and charge?discharge current. Two step-by-step tutorials and model examples for applying this methodology are also provided. The proposed methodology is anticipated to stimulate continued dialogue among researchers, fostering advancements in achieving stable and high-performance supercapacitor devices.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">n/a</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kholimatussadiah, Septia</style></author><author><style face="normal" font="default" size="100%">Hsu, Chia-Ling</style></author><author><style face="normal" font="default" size="100%">Ke, Shang-Wei</style></author><author><style face="normal" font="default" size="100%">Tsu-chin Chou</style></author><author><style face="normal" font="default" size="100%">Wu, Yung-Fu</style></author><author><style face="normal" font="default" size="100%">Yakimova, Rositsa</style></author><author><style face="normal" font="default" size="100%">Kumatani, Akichika</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">He-Yun Du</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In-situ observation of hydrogen nanobubbles formation on graphene surface by AFM-SECM</style></title><secondary-title><style face="normal" font="default" size="100%">Electrochimica Acta</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Atomic force microscopy</style></keyword><keyword><style  face="normal" font="default" size="100%">graphene</style></keyword><keyword><style  face="normal" font="default" size="100%">Hydrogen bubble</style></keyword><keyword><style  face="normal" font="default" size="100%">hydrogen evolution reaction</style></keyword><keyword><style  face="normal" font="default" size="100%">Scanning electrochemical microscopy</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2024</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0013468624006662</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">493</style></volume><pages><style face="normal" font="default" size="100%">144425</style></pages><isbn><style face="normal" font="default" size="100%">0013-4686</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Gas bubble evolution is an important phenomenon in many electrochemical processes and it is highly sensitive to the surface properties. Here we visualize the gas bubble dynamics on the surface of different graphene substrates during hydrogen evolution reaction (HER) using atomic force microscopy combined with scanning electrochemical microscopy. The low overpotential and low surface hydrophobicity of few-layer graphene formed on C-phase SiC causes the uniform distribution of hydrogen nanobubbles, which easily depart from the surface during the reaction. Conversely, the high overpotential and more hydrophobic surface of HOPG induces hydrogen bubbles to linger on the surface for an extended duration, leading to its accumulation and the subsequent formation of microbubbles. This in-situ nanoscale electrochemical mapping of hydrogen bubble dynamics provides new insight into electrocatalytic HER that occurs on non-metal electrodes.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hammad Elsayed, Mohamed</style></author><author><style face="normal" font="default" size="100%">Abdellah, Mohamed</style></author><author><style face="normal" font="default" size="100%">Alhakemy, Ahmed Zaki</style></author><author><style face="normal" font="default" size="100%">Mekhemer, Islam M. A.</style></author><author><style face="normal" font="default" size="100%">Aboubakr, Ahmed Esmail A.</style></author><author><style face="normal" font="default" size="100%">Chen, Bo-Han</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Lin, Kun-Han</style></author><author><style face="normal" font="default" size="100%">Chiu, Wen-Sheng</style></author><author><style face="normal" font="default" size="100%">Lin, Sheng-Jie</style></author><author><style face="normal" font="default" size="100%">Chu, Che-Yi</style></author><author><style face="normal" font="default" size="100%">Lu, Chih-Hsuan</style></author><author><style face="normal" font="default" size="100%">Yang, Shang-Da</style></author><author><style face="normal" font="default" size="100%">Mohamed, Mohamed Gamal</style></author><author><style face="normal" font="default" size="100%">Kuo, Shiao-Wei</style></author><author><style face="normal" font="default" size="100%">Hung, Chen-Hsiung</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Chou, Ho-Hsiu</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Overcoming small-bandgap charge recombination in visible and NIR-light-driven hydrogen evolution by engineering the polymer photocatalyst structure</style></title><secondary-title><style face="normal" font="default" size="100%">Nature Communications</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2024</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1038/s41467-024-45085-6</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">707</style></pages><isbn><style face="normal" font="default" size="100%">2041-1723</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Designing an organic polymer photocatalyst for efficient hydrogen evolution with visible and near-infrared (NIR) light activity is still a major challenge. Unlike the common behavior of gradually increasing the charge recombination while shrinking the bandgap, we present here a series of polymer nanoparticles (Pdots) based on ITIC and BTIC units with different π-linkers between the acceptor-donor-acceptor (A-D-A) repeated moieties of the polymer. These polymers act as an efficient single polymer photocatalyst for H2 evolution under both visible and NIR light, without combining or hybridizing with other materials. Importantly, the difluorothiophene (ThF) π-linker facilitates the charge transfer between acceptors of different repeated moieties (A-D-A-(π-Linker)-A-D-A), leading to the enhancement of charge separation between D and A. As a result, the PITIC-ThF Pdots exhibit superior hydrogen evolution rates of 279 µmol/h and 20.5 µmol/h with visible (&amp;gt;420 nm) and NIR (&amp;gt;780 nm) light irradiation, respectively. Furthermore, PITIC-ThF Pdots exhibit a promising apparent quantum yield (AQY) at 700 nm (4.76%).&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hailemariam, Adane G.</style></author><author><style face="normal" font="default" size="100%">Syum, Zeru</style></author><author><style face="normal" font="default" size="100%">Mamo, Tadios T.</style></author><author><style face="normal" font="default" size="100%">Mohammad Qorbani</style></author><author><style face="normal" font="default" size="100%">Hsing, Cheng-Rong</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Quadir, Shaham</style></author><author><style face="normal" font="default" size="100%">Bayikadi, Khasim S.</style></author><author><style face="normal" font="default" size="100%">Heng-Liang Wu</style></author><author><style face="normal" font="default" size="100%">Wei, Ching-Ming</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Oxygen-Incorporated Lithium-Rich Iron Sulfide Cathodes for Li-Ion Batteries with Boosted Material Stability and Electrochemical Performance</style></title><secondary-title><style face="normal" font="default" size="100%">Chemistry of MaterialsChemistry of Materials</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2024</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acs.chemmater.4c00508</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">36</style></volume><pages><style face="normal" font="default" size="100%">9370 - 9379</style></pages><isbn><style face="normal" font="default" size="100%">0897-4756</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">n/a</style></abstract><issue><style face="normal" font="default" size="100%">19</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;doi: 10.1021/acs.chemmater.4c00508&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Krishnamoorthy, Vimal</style></author><author><style face="normal" font="default" size="100%">Sabhapathy, Palani</style></author><author><style face="normal" font="default" size="100%">Raghunath, Puttikam</style></author><author><style face="normal" font="default" size="100%">Huang,Chih-Yang</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Kamal Hussien, Mahmoud</style></author><author><style face="normal" font="default" size="100%">Syum, Zeru</style></author><author><style face="normal" font="default" size="100%">Muthusamy, Saravanakumar</style></author><author><style face="normal" font="default" size="100%">Lin, Ming-Chang</style></author><author><style face="normal" font="default" size="100%">Heng-Liang Wu</style></author><author><style face="normal" font="default" size="100%">Ruei-San Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synergistic Electronic Interaction of Nitrogen Coordinated Fe-Sn Double-Atom Sites: An Efficient Electrocatalyst for Oxygen Reduction Reaction</style></title><secondary-title><style face="normal" font="default" size="100%">Small Methods</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">d-block metal</style></keyword><keyword><style  face="normal" font="default" size="100%">Double-atom sites</style></keyword><keyword><style  face="normal" font="default" size="100%">Fe-Sn-N/C</style></keyword><keyword><style  face="normal" font="default" size="100%">oxygen reduction</style></keyword><keyword><style  face="normal" font="default" size="100%">P-block metal</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2024</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/smtd.202301674</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><volume><style face="normal" font="default" size="100%">n/a</style></volume><pages><style face="normal" font="default" size="100%">2301674</style></pages><isbn><style face="normal" font="default" size="100%">2366-9608</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Abstract Double-atom site catalysts (DASs) have emerged as a recent trend in the oxygen reduction reaction (ORR), thereby modifying the intermediate adsorption energies and increasing the activity. However, the lack of an efficient dual atom site to improve activity and durability has limited these catalysts from widespread application. Herein, the nitrogen-coordinated iron and tin-based DASs (Fe-Sn-N/C) catalyst are synthesized for ORR. This catalyst has a high activity with ORR half-wave potentials (E1/2) of 0.92 V in alkaline, which is higher than those of the state-of-the-art Pt/C (E1/2 = 0.83 V), Fe-N/C (E1/2 = 0.83 V), and Sn-N/C (E1/2 = 0.77 V). Scanning electron transmission microscopy analysis confirmed the atomically distributed Fe and Sn sites on the N-doped carbon network. X-ray absorption spectroscopy analysis revealed the charge transfer between Fe and Sn. Both experimental and theoretical results indicate that the Sn with Fe-NC (Fe-Sn-N/C) induces charge redistribution, weakening the binding strength of oxygenated intermediates and leading to improved ORR activity. This study provides the synergistic effects of DASs catalysts and addresses the impacts of P-block elements on d-block transition metals in ORR.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">n/a</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Thang, Nguyen Quoc</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Huang,Chih-Yang</style></author><author><style face="normal" font="default" size="100%">Phuong, Nguyen Hoang</style></author><author><style face="normal" font="default" size="100%">Lin, Tsai-Yu</style></author><author><style face="normal" font="default" size="100%">Kamal Hussien, Mahmoud</style></author><author><style face="normal" font="default" size="100%">Heng-Liang Wu</style></author><author><style face="normal" font="default" size="100%">Chih-I Wu</style></author><author><style face="normal" font="default" size="100%">Pham, Nguyet N. T.</style></author><author><style face="normal" font="default" size="100%">Viet, Pham Van</style></author><author><style face="normal" font="default" size="100%">Chih-Hao Lee</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Tailoring atomically dispersed Fe-induced oxygen vacancies for highly efficient gas-phase photocatalytic CO2 reduction and NO removal with diminished noxious byproducts</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2024</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D4TA05778C</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">31847 - 31860</style></pages><isbn><style face="normal" font="default" size="100%">2050-7488</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Single-atom-supported metal oxides have attracted extensive interest in energy catalysis, offering a promising avenue for mitigating greenhouse gas emissions and environmental pollution. This study presents a facile synthesis of single-atom Fe-modified Bi2WO6 photocatalysts. By carefully tuning the Fe ratios, the 1.5Fe-Bi2WO6 sample demonstrates exceptional photocatalytic efficiency in CO2 to CO reduction (36.78 μmol g−1). Additionally, an outstanding NO removal performance is also achieved through this photocatalyst with an impressively low conversion of toxic NO2 at just 0.37%. The reaction intermediates and mechanisms governing the photocatalytic reduction of CO2 into CO are elucidated using in situ DRIFTS and in situ XAS techniques. Regarding NO removal, the introduction of Fe single-atoms, along with induced oxygen vacancies, plays a pivotal role in facilitating the transformation of NO and NO2 into nitrate by stabilizing NO and NO2 species. Mechanistic insights into photocatalytic NO oxidation are garnered through scavenger trapping and EPR experiments employing DMPO. This study emphasizes single-atom-supported metal oxide's potential in sustainable chemistry and air purification, providing a promising solution for urgent environmental challenges.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">46</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bayikadi, Khasim Saheb</style></author><author><style face="normal" font="default" size="100%">Imam, Safdar</style></author><author><style face="normal" font="default" size="100%">Tee, Wei-Shen</style></author><author><style face="normal" font="default" size="100%">Kavirajan, Sugumaran</style></author><author><style face="normal" font="default" size="100%">Chang, Chiao-Yu</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Fang-Yu Fu</style></author><author><style face="normal" font="default" size="100%">Liu, Ting-Ran</style></author><author><style face="normal" font="default" size="100%">Chiang, Ching-Yu</style></author><author><style face="normal" font="default" size="100%">Shukla, Dinesh</style></author><author><style face="normal" font="default" size="100%">Chien-Ting Wu</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Chou, Mei-Yin</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Raman Sankar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ultra-low lattice thermal conductivity driven high thermoelectric figure of merit in Sb/W co-doped GeTe</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2024</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D4TA05332J</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">30892 - 30905</style></pages><isbn><style face="normal" font="default" size="100%">2050-7488</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;High thermoelectric performance is a material challenge associated mainly with the manipulation of lattice dynamics to obtain extrinsic phonon transport routes, which can make the lattice thermal conductivity (κlat) intrinsically low by introducing multiple scattering mechanisms. The present study shows that the lattice-strain-induced phonon scattering resulting from microstructural distortions in GeTe-based compounds can enable ultralow lattice thermal conductivity. The unusual lattice shrinkage, W interstitials, W nanoprecipitates, and heavy elemental mass, in Ge0.85Sb0.1W0.05Te culminate in an ultralow lattice thermal conductivity of ∼0.2 W m−1 K−1 at 825 K. Microstructural distortions in this Sb/W co-doped GeTe are found to be primarily associated with shorter W–Te bonding owing to the anomalous effect of the higher electronegativity of the W atoms. Furthermore, the increased electrical conductivity (σ) resulting from the enhanced vacancy formation caused by W doping and W interstitials synergistically contributes to optimization of the thermoelectric performance (ZT) to ∼2.93 at 825 K. The thermoelectric efficiency (η) as high as ∼17% has been obtained for a single leg in this composition at an operating temperature of 825 K, with an estimated device ZT value of ∼1.38.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">44</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Huang,Chih-Yang</style></author><author><style face="normal" font="default" size="100%">Tseng, Shao-Chin</style></author><author><style face="normal" font="default" size="100%">Wei-ChaoChen</style></author><author><style face="normal" font="default" size="100%">Yin, Gung-Chian</style></author><author><style face="normal" font="default" size="100%">Chen, Bo-Yi</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Cheng-YingChen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Visualization of Anion Vacancy Defect Annihilation in CZTSe Solar Cells by Hydrogen-Assisted Selenization with In Operando X-ray Nanoprobe Studies</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; InterfacesACS Applied Materials &amp; Interfaces</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2024</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acsami.4c11127</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">64656 - 64663</style></pages><isbn><style face="normal" font="default" size="100%">1944-8244</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">n/a</style></abstract><issue><style face="normal" font="default" size="100%">47</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;doi: 10.1021/acsami.4c11127&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>6</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chen, L.</style></author><author><style face="normal" font="default" size="100%">Chen, W.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Applications Of X-ray Techniques To Nanomaterials For Energy Research</style></title><tertiary-title><style face="normal" font="default" size="100%">World Scientific Series In Nanoscience And Nanotechnology</style></tertiary-title></titles><dates><year><style  face="normal" font="default" size="100%">2024</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://books.google.com.tw/books?id=1pn7EAAAQBAJ</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">World Scientific Publishing Company</style></publisher><isbn><style face="normal" font="default" size="100%">9789811284656</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">n/a</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Indrajit Shown</style></author><author><style face="normal" font="default" size="100%">Wei-Fu Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Applications of X-ray Spectroscopy in Carbon Dioxide Reduction</style></title><secondary-title><style face="normal" font="default" size="100%">Applications of X-ray Techniques to Nanomaterials for Energy Research</style></secondary-title><tertiary-title><style face="normal" font="default" size="100%">World Scientific Series in Nanoscience and Nanotechnology</style></tertiary-title></titles><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2023/08/30</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1142/9789811284649_0005</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">WORLD SCIENTIFIC</style></publisher><volume><style face="normal" font="default" size="100%">Volume 24</style></volume><pages><style face="normal" font="default" size="100%">155-186</style></pages><isbn><style face="normal" font="default" size="100%">978-981-12-8463-2</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The following sections are included: Introduction XAS for CO2 Reduction Electrochemical CO2 Reduction Photochemical CO2 Reduction Summary and Proposed Research Prospects Acknowledgments ReferencesThe following sections are included: Introduction XAS for CO2 Reduction Electrochemical CO2 Reduction Photochemical CO2 Reduction Summary and Proposed Research Prospects Acknowledgments References&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;doi:10.1142/9789811284649_0005&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sabhapathy, Palani</style></author><author><style face="normal" font="default" size="100%">Raghunath, Puttikam</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Indrajit Shown</style></author><author><style face="normal" font="default" size="100%">Bayikadi, Khasim Saheb</style></author><author><style face="normal" font="default" size="100%">Xie, Rui-Kun</style></author><author><style face="normal" font="default" size="100%">Krishnamoorthy, Vimal</style></author><author><style face="normal" font="default" size="100%">Lin, Ming-Chang</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Axial Chlorine Induced Electron Delocalization in Atomically Dispersed FeN4 Electrocatalyst for Oxygen Reduction Reaction with Improved Hydrogen Peroxide Tolerance</style></title><secondary-title><style face="normal" font="default" size="100%">Small</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cl coordination</style></keyword><keyword><style  face="normal" font="default" size="100%">d-band center</style></keyword><keyword><style  face="normal" font="default" size="100%">electron density</style></keyword><keyword><style  face="normal" font="default" size="100%">FeN4</style></keyword><keyword><style  face="normal" font="default" size="100%">Fenton reaction</style></keyword><keyword><style  face="normal" font="default" size="100%">oxygen reduction reaction</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2023</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/smll.202303598</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><pages><style face="normal" font="default" size="100%">2303598</style></pages><isbn><style face="normal" font="default" size="100%">1613-6810</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Abstract Atomically dispersed iron sites on nitrogen-doped carbon (Fe-NC) are the most active Pt-group-metal-free catalysts for oxygen reduction reaction (ORR). However, due to oxidative corrosion and the Fenton reaction, Fe-NC catalysts are insufficiently active and stable. Herein, w e demonstrated that the axial Cl-modified Fe-NC (Cl-Fe-NC) electrocatalyst is active and stable for the ORR in acidic conditions with high H2O2 tolerance. The Cl-Fe-NC exhibits excellent ORR activity, with a high half-wave potential (E1/2) of 0.82 V versus a reversible hydrogen electrode (RHE), comparable to Pt/C (E1/2 = 0.85 V versus RHE) and better than Fe-NC (E1/2 = 0.79 V versus RHE). X-ray absorption spectroscopy analysis confirms that chlorine is axially integrated into the FeN4. More interestingly, compared to Fe-NC, the Fenton reaction is markedly suppressed in Cl-Fe-NC. In situ electrochemical impedance spectroscopy reveals that Cl-Fe-NC provides efficient electron transfer and faster reaction kinetics than Fe-NC. Density functional theory calculations reveal that incorporating Cl into FeN4 can drive the electron density delocalization of the FeN4 site, leading to a moderate adsorption free energy of OH* (?GOH*), d-band center, and a high onset potential, and promotes the direct four-electron-transfer ORR with weak H2O2 binding ability compared to Cl-free FeN4, indicating superior intrinsic ORR activity.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;&lt;a href=&quot;https://doi.org/10.1002/smll.202303598&quot; rel=&quot;nofollow&quot;&gt;https://doi.org/10.1002/smll.202303598&lt;/a&gt;&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Syum, Zeru</style></author><author><style face="normal" font="default" size="100%">Tadesse Billo</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Anbalagan, Aswin kumar</style></author><author><style face="normal" font="default" size="100%">Quadir, Shaham</style></author><author><style face="normal" font="default" size="100%">Hailemariam, Adane Gebresilassie</style></author><author><style face="normal" font="default" size="100%">Sabhapathy, Palani</style></author><author><style face="normal" font="default" size="100%">Chih-Hao Lee</style></author><author><style face="normal" font="default" size="100%">Heng-Liang Wu</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhancing the lithium-ion storage capability of Cu2ZnSnS4 anodes via a nitrogen-doped conductive support</style></title><secondary-title><style face="normal" font="default" size="100%">Chemical Engineering Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Conductive support</style></keyword><keyword><style  face="normal" font="default" size="100%">Lithium-ion battery</style></keyword><keyword><style  face="normal" font="default" size="100%">polyaniline (PANI) modify CZTS</style></keyword><keyword><style  face="normal" font="default" size="100%">RAMAN</style></keyword><keyword><style  face="normal" font="default" size="100%">XAS</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2023</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S1385894723015176</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">465</style></volume><pages><style face="normal" font="default" size="100%">142786</style></pages><isbn><style face="normal" font="default" size="100%">1385-8947</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Achieving lithium-ion batteries with both excellent electrochemical performance and cycling stability is a top priority for their real-world applications. This work reports high-performance and stable Cu2ZnSnS4 (CZTS) anode materials encapsulated by nitrogen-doped carbon (CZTS@N-C) for advanced lithium-ion battery application. Ex-situ X-ray photoelectron spectroscopy and transmission electron microscopy revealed that the nitrogen-doped carbon network features a more conducive solid-electrolyte interphase that enables lower charge-transfer resistance and fast Li+ diffusion kinetics with negligible initial irreversible capacity loss. As a result, the CZTS@N-C electrode delivers a significantly enhanced capacity of 710 mAh g−1 with 73% capacity retention after 220 cycles at a current rate of 0.5 mA g−1 and superior rate performance compared to that of unmodified CZTS. Additionally, the study sheds light on the fast lithiation dynamics chemistry of CZTS@N-C through kinetics analysis, explored by in-situ Raman, ex-situ X-ray absorption, and in-situ electrochemical impedance. This study provides a new approach for fabricating high-performance, durable conductive polymer-encapsulated low-cost transition-metal-sulfide anode materials.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Muthusamy, Saravanakumar</style></author><author><style face="normal" font="default" size="100%">Sabhapathy, Palani</style></author><author><style face="normal" font="default" size="100%">Putikam Raghunath</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Chang, Yu-Chung</style></author><author><style face="normal" font="default" size="100%">Krishnamoorthy, Vimal</style></author><author><style face="normal" font="default" size="100%">Ho, Thi-Thong</style></author><author><style face="normal" font="default" size="100%">Chiou, Jau-Wern</style></author><author><style face="normal" font="default" size="100%">Lin, Ming-Chang</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Mimicking Metalloenzyme Microenvironments in the Transition Metal-Single Atom Catalysts for Electrochemical Hydrogen Peroxide Synthesis in an Acidic Medium</style></title><secondary-title><style face="normal" font="default" size="100%">Small Methods</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">d-band center</style></keyword><keyword><style  face="normal" font="default" size="100%">Electrocatalysis</style></keyword><keyword><style  face="normal" font="default" size="100%">electrochemical H2O2 production</style></keyword><keyword><style  face="normal" font="default" size="100%">electronic structures</style></keyword><keyword><style  face="normal" font="default" size="100%">oxygen reduction reaction</style></keyword><keyword><style  face="normal" font="default" size="100%">single-atom catalysts</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2023</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/smtd.202300234</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><pages><style face="normal" font="default" size="100%">2300234</style></pages><isbn><style face="normal" font="default" size="100%">2366-9608</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Abstract Electrochemical reduction of oxygen into hydrogen peroxide in an acidic medium offers an energy-efficient and green H2O2 synthesis as an alternative to the energy-intensive anthraquinone process. Unfortunately, high overpotential, low production rates, and fierce competition from traditional four-electron reduction limit it. In this study, a metalloenzyme-like active structure is mimicked in carbon-based single-atom electrocatalysts for oxygen reduction to H2O2. Using a carbonization strategy, the primary electronic structure of the metal center with nitrogen and oxygen coordination is modulated, followed by epoxy oxygen functionalities close to the metal active sites. In an acidic medium, CoNOC active structures proceed with greater than 98% H2O2 selectivity (2e?/2H+) rather than CoNC active sites that are selective to H2O (4e?/4H+). Among all MNOC (M = Fe, Co, Mn, and Ni) single-atom electrocatalysts, the CoNOC is the most selective (&amp;gt; 98%) for H2O2 production, with a mass activity of 10 A g?1 at 0.60 V vs. RHE. X-ray absorption spectroscopy is used to identify the formation of unsymmetrical MNOC active structures. Experimental results are also compared to density functional theory calculations, which revealed that the structure-activity relationship of the epoxy-surrounded CoNOC active structure reaches optimum (?G*OOH) binding energies for high selectivity.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;&lt;a href=&quot;https://doi.org/10.1002/smtd.202300234&quot; rel=&quot;nofollow&quot;&gt;https://doi.org/10.1002/smtd.202300234&lt;/a&gt;&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Muthusamy, Saravanakumar</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Sabhapathy, Palani</style></author><author><style face="normal" font="default" size="100%">Chang, Yu-Chung</style></author><author><style face="normal" font="default" size="100%">Tadesse Billo</style></author><author><style face="normal" font="default" size="100%">Syum, Zeru</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Modification of Conductive Carbon with N-Coordinated Fe−Co Dual-Metal Sites for Oxygen Reduction Reaction</style></title><secondary-title><style face="normal" font="default" size="100%">ChemElectroChem</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">conductive carbon</style></keyword><keyword><style  face="normal" font="default" size="100%">dual metal-atom catalysts</style></keyword><keyword><style  face="normal" font="default" size="100%">Electrocatalysis</style></keyword><keyword><style  face="normal" font="default" size="100%">oxygen reduction</style></keyword><keyword><style  face="normal" font="default" size="100%">polyurea aerogels</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2023</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/celc.202300272</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><volume><style face="normal" font="default" size="100%">n/a</style></volume><pages><style face="normal" font="default" size="100%">e202300272</style></pages><isbn><style face="normal" font="default" size="100%">2196-0216</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Abstract Earth-abundant commercial conductive carbon materials are ideal electrocatalyst supports but cannot be directly utilized for single-atom catalysts owing to the lack of anchoring sites. Therefore, we employed crosslink polymerization to modify the conductive carbon surface with Fe?Co dual-site electrocatalysts for oxygen reduction reaction (ORR). First, metal-coordinated polyurea (PU) aerogels were prepared using via crosslinked polymerization at ambient temperature. Then, carbon-supported, atomically dispersed Fe?Co dual-atom sites (FeCoNC/BP) were formed by high-temperatures pyrolysis with a nitrogen source. FTIR and 13C NMR measurements showed PU linkages, while 15N NMR revealed metal?nitrogen coordination in the PU gels. Asymmetric, N-coordinated, and isolated Fe?Co active structures were found after pyrolysis using XAS and STEM. In alkaline media, FeCoNC/BP exhibited excellent ORR activity, with a E1/2 of 0.93?V vs. RHE, higher than that of Pt/C (20?%) (0.90?V), FeNC/BP (0.88?V), and CoNC/BP (0.85?V). An accelerated durability test (ADT) on FeCoNC/BP indicated good durability over 35000 cycles. FeCoNC/BP also showed moderate ORR and ADT performance in acidic media. The macro/mesoporous N-doped carbon structures enhanced the mass transport properties of the dual Fe?Co active-sites. Therefore, modifying carbon supports with nonprecious metal catalysts may be a cost-effective-strategy for sustained electrochemical energy conversion.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">n/a</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kamal Hussien, Mahmoud</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Mohammad Qorbani</style></author><author><style face="normal" font="default" size="100%">Hammad Elsayed, Mohamed</style></author><author><style face="normal" font="default" size="100%">Quadir, Shaham</style></author><author><style face="normal" font="default" size="100%">Putikam Raghunath</style></author><author><style face="normal" font="default" size="100%">Tzou, Der-Lii M.</style></author><author><style face="normal" font="default" size="100%">Haw, Shu-Chih</style></author><author><style face="normal" font="default" size="100%">Chou, Ho-Hsiu</style></author><author><style face="normal" font="default" size="100%">Thang, Nguyen Quoc</style></author><author><style face="normal" font="default" size="100%">M.-C. Lin</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Numerous defects induced by exfoliation of boron-doped g-C3N4 towards active sites modulation for highly efficient solar-to-fuel conversion</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Today Sustainability</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">CO reduction</style></keyword><keyword><style  face="normal" font="default" size="100%">Delamination</style></keyword><keyword><style  face="normal" font="default" size="100%">Exciton dissociation</style></keyword><keyword><style  face="normal" font="default" size="100%">Graphitic carbon nitride</style></keyword><keyword><style  face="normal" font="default" size="100%">Hydrogen evolution</style></keyword><keyword><style  face="normal" font="default" size="100%">Photocatalyst</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2023</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S2589234723000453</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">22</style></volume><pages><style face="normal" font="default" size="100%">100359</style></pages><isbn><style face="normal" font="default" size="100%">2589-2347</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Graphitic carbon nitride (CN) has emerged as a highly promising material in the photocatalysis field. However, its bulk structure suffers from a lack of active sites, limiting its practical application. Herein, a boron-doped CN (BCN) was prepared by a green gas-blowing-assisted thermal polymerization and then subjected to different exfoliation processes in order to delaminate the layered structure and tune the surface-active sites. A thorough comparative study shows that thermal exfoliation creates unsaturated nitrogen sites and induces the formation of interconnected layers that act as an electron diffusion channel for better charge transport. Furthermore, the thermally exfoliated BCN is rich in structural disorders that serve as dissociation defects for photoinduced charge carriers with a low exciton binding energy of 27 meV. Experimental results supported by theoretical calculations show that the nitrogen adjacent to boron is activated by the surrounding surface amino groups and the perforated texture to serve as an active adsorption site towards CO2 and H2O. Consequently, the exfoliated BCN acts as an outstanding bifunctional photocatalyst towards CO2 reduction into CO (40.41 μmol g−1 h−1) and prominent hydrogen evolution (4740 μmol g−1 h−1, 12.2% apparent quantum yield (AQY)).&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mohammad Qorbani</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Lai, Ying-Ren</style></author><author><style face="normal" font="default" size="100%">Kholimatussadiah, Septia</style></author><author><style face="normal" font="default" size="100%">Quadir, Shaham</style></author><author><style face="normal" font="default" size="100%">Huang,Chih-Yang</style></author><author><style face="normal" font="default" size="100%">Indrajit Shown</style></author><author><style face="normal" font="default" size="100%">Yi-Fan Huang</style></author><author><style face="normal" font="default" size="100%">Hayashi, Michitoshi</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Atomistic insights into highly active reconstructed edges of monolayer 2H-WSe2 photocatalyst</style></title><secondary-title><style face="normal" font="default" size="100%">Nature Communications</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1038/s41467-022-28926-0</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">1256</style></pages><isbn><style face="normal" font="default" size="100%">2041-1723</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Ascertaining the function of in-plane intrinsic defects and edge atoms is necessary for developing efficient low-dimensional photocatalysts. We report the wireless photocatalytic CO2 reduction to CH4 over reconstructed edge atoms of monolayer 2H-WSe2 artificial leaves. Our first-principles calculations demonstrate that reconstructed and imperfect edge configurations enable CO2 binding to form linear and bent molecules. Experimental results show that the solar-to-fuel quantum efficiency is a reciprocal function of the flake size. It also indicates that the consumed electron rate per edge atom is two orders of magnitude larger than the in-plane intrinsic defects. Further, nanoscale redox mapping at the monolayer WSe2–liquid interface confirms that the edge is the most preferred region for charge transfer. Our results pave the way for designing a new class of monolayer transition metal dichalcogenides with reconstructed edges as a non-precious co-catalyst for wired or wireless hydrogen evolution or CO2 reduction reactions.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Indrajit Shown</style></author><author><style face="normal" font="default" size="100%">Mohammad Qorbani</style></author><author><style face="normal" font="default" size="100%">Fang-Yu Fu</style></author><author><style face="normal" font="default" size="100%">Lin, Tsai-Yu</style></author><author><style face="normal" font="default" size="100%">Heng-Liang Wu</style></author><author><style face="normal" font="default" size="100%">Chung, Po-Wen</style></author><author><style face="normal" font="default" size="100%">Chih-I. Wu</style></author><author><style face="normal" font="default" size="100%">Santiago, Svette Reina Merden</style></author><author><style face="normal" font="default" size="100%">Ji-Lin Shen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Boosting photocatalytic CO2 reduction in a ZnS/ZnIn2S4 heterostructure through strain-induced direct Z-scheme and a mechanistic study of molecular CO2 interaction thereon</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">CO reduction</style></keyword><keyword><style  face="normal" font="default" size="100%">Interfacial charge transfer</style></keyword><keyword><style  face="normal" font="default" size="100%">Photocatalysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Z-Scheme</style></keyword><keyword><style  face="normal" font="default" size="100%">ZnInS</style></keyword><keyword><style  face="normal" font="default" size="100%">ZnS</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S2211285521010582</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">93</style></volume><pages><style face="normal" font="default" size="100%">106809</style></pages><isbn><style face="normal" font="default" size="100%">2211-2855</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Employing direct Z-scheme semiconductor heterostructures in photocatalysis offers efficient charge carrier separation and isolation of both redox reactions, thus beneficial to reduce CO2 into solar fuels. Here, a ZnS/ZnIn2S4 heterostructure, comprising cubic ZnS nanocrystals on hexagonal ZnIn2S4 (ZIS) nanosheets, is successfully fabricated in a single-pot hydrothermal approach. The composite ZnS/ZnIn2S4 exhibits microstrain at its interface with an electric field favorable for Z-scheme. At an optimum ratio of Zn:In (~ 1:0.5), an excellent photochemical quantum efficiency of around 0.8% is reached, nearly 200-fold boost compared with pristine ZnS. Electronic levels and band alignments are deduced from ultraviolet photoemission spectroscopy and UV-Vis. Evidence of the direct Z-scheme and carrier dynamics is verified by photo-reduction experiment, along with photoluminescence (PL) and time-resolved PL. Finally, diffuse-reflectance infrared Fourier transformed spectroscopy explores the CO2 and related intermediate species adsorbed on the catalyst during the photocatalytic reaction. This microstrain-induced direct Z-scheme approach opens a new pathway for developing next-generation photocatalysts for CO2 reduction.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Fahimi, Zohre</style></author><author><style face="normal" font="default" size="100%">Moradlou, Omran</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Mohammad Qorbani</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Co3V2O8 hollow spheres with mesoporous walls as high-capacitance electrode for hybrid supercapacitor device</style></title></titles><keywords><keyword><style  face="normal" font="default" size="100%">bimetal oxide</style></keyword><keyword><style  face="normal" font="default" size="100%">hollow sphere</style></keyword><keyword><style  face="normal" font="default" size="100%">hybrid device</style></keyword><keyword><style  face="normal" font="default" size="100%">mesoporous</style></keyword><keyword><style  face="normal" font="default" size="100%">STABILITY</style></keyword><keyword><style  face="normal" font="default" size="100%">SUPERCAPACITOR</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S1385894722007306</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">436</style></volume><pages><style face="normal" font="default" size="100%">135225</style></pages><isbn><style face="normal" font="default" size="100%">1385-8947</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Bimetal oxides are promising materials in the field of energy storage due to their various oxidation states, synergistic interactions among multiple metal species, and stability. In this work, Co3V2O8 hollow spheres are synthesized by a two-step hydrothermal method: (i) synthesis of V2O5 spheres and (ii) partial replacement of V by Co through the Kirkendall effect. As an electrode, it shows an extrinsic pseudocapacitive charge-storage mechanism due to different oxidation states of V and Co ions. Because of the low crystallinity degree of the mesoporous wall and high accessible surface area of hollow spheres, the optimum Co3V2O8 electrode reaches a high specific capacitance of 2376F g−1 at a current density of 2 A g−1, which is more than two times higher than the top reported values, and a rate capability retention of ∼80% at 20 A g−1. Using Co3V2O8, activated carbon, and KOH as positive, negative electrodes, and electrolyte, respectively, a hybrid supercapacitor device presents maximum energy and power densities of 59.2 Wh kg−1 and 36.6 kW kg−1, respectively. Further, the aqueous supercapacitor device shows superior structural and electrochemical stabilities after 10,000 galvanostatic charge–discharge cycles because of the arrays of voids in the orthorhombic crystal structure of Co3V2O8 that can decrease the volume expansion/shrinkage during the intercalation/deintercalation processes. Our results provide a platform for exploring bimetallic Co and V-based oxides, hydroxides, and sulfides nanostructures as promising energy storage materials in the future.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bayikadi, Khasim Saheb</style></author><author><style face="normal" font="default" size="100%">Imam, Safdar</style></author><author><style face="normal" font="default" size="100%">Ubaid, Mohammad</style></author><author><style face="normal" font="default" size="100%">Aziz, Anver</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Raman Sankar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of aliovalent substituted highly disordered GeTe compound's thermoelectric performance</style></title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Atomic disorder</style></keyword><keyword><style  face="normal" font="default" size="100%">Doping optimization</style></keyword><keyword><style  face="normal" font="default" size="100%">Figure of merit</style></keyword><keyword><style  face="normal" font="default" size="100%">thermal conductivity</style></keyword><keyword><style  face="normal" font="default" size="100%">Vacancy control</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0925838822026123</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">922</style></volume><pages><style face="normal" font="default" size="100%">166221</style></pages><isbn><style face="normal" font="default" size="100%">0925-8388</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;As a lead-free high-performance thermoelectric material, germanium telluride (GeTe) has recently been extensively studied for mid-temperature (500–800 K) applications. The carrier concentration and the thermal conductivity are reduced for vacancy-controlled GeTe compounds compared with pristine GeTe. We explored and optimized the Ge0.9−xSb0.1PxTe (x = 0.01–0.05) material's highest thermoelectric performance at elevated temperatures. Intrinsic Ge vacancy control and manipulation of Ge (+2) with Sb/P (+3) increased the charge contribution to power factor improvement to ∼42 µWcm−1 K−2 while minimizing the lattice thermal contribution to ∼0.4 W/mK. This resulted in an increase in thermoelectric performance of ∼2.4 @ 773 K for the Ge0.88Sb0.1P0.02Te sample. The inclusion of atomically disordered Sb/P ions considerably increases the scattering effects caused by the point defect, whereas stretched grain boundaries reveal the decreased lattice thermal contribution. The current work demonstrates the effectiveness of phosphorus as a co-dopant in increasing the average thermoelectric performance (ZTavg) value over the GeTe operating temperature range.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Valiyaveettil, Suneesh Meledath</style></author><author><style face="normal" font="default" size="100%">Nguyen, Duc-Long</style></author><author><style face="normal" font="default" size="100%">Deniz P. Wong</style></author><author><style face="normal" font="default" size="100%">Hsing, Cheng-Rong</style></author><author><style face="normal" font="default" size="100%">Paradis-Fortin, Laura</style></author><author><style face="normal" font="default" size="100%">Mohammad Qorbani</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Chou, Ta-Lei</style></author><author><style face="normal" font="default" size="100%">Wu, Kuei-Kuan</style></author><author><style face="normal" font="default" size="100%">Rathinam, Vasudevan</style></author><author><style face="normal" font="default" size="100%">Wei, Ching-Ming</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhanced Thermoelectric Performance in Ternary Skutterudite Co(Ge0.5Te0.5)3 via Band Engineering</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acs.inorgchem.1c03947</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><isbn><style face="normal" font="default" size="100%">0020-1669</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;doi: 10.1021/acs.inorgchem.1c03947&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Valiyaveettil, Suneesh Meledath</style></author><author><style face="normal" font="default" size="100%">Mohammad Qorbani</style></author><author><style face="normal" font="default" size="100%">Hsing, Cheng-Rong</style></author><author><style face="normal" font="default" size="100%">Chou, Ta-Lei</style></author><author><style face="normal" font="default" size="100%">Paradis-Fortin, Laura</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Srivastava, Divya</style></author><author><style face="normal" font="default" size="100%">Nguyen, Duc-Long</style></author><author><style face="normal" font="default" size="100%">Ho, Thi-Thong</style></author><author><style face="normal" font="default" size="100%">Tadesse Billo</style></author><author><style face="normal" font="default" size="100%">Ganesan, Peramaiyan</style></author><author><style face="normal" font="default" size="100%">Wei, Ching-Ming</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhanced thermoelectric performance of skutterudite Co1−yNiySn1.5Te1.5−x with switchable conduction behavior</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Today Physics</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Density functional theory</style></keyword><keyword><style  face="normal" font="default" size="100%">Phonon scattering</style></keyword><keyword><style  face="normal" font="default" size="100%">Skutterudite</style></keyword><keyword><style  face="normal" font="default" size="100%">Switchable carrier type</style></keyword><keyword><style  face="normal" font="default" size="100%">Thermoelectrics</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S2542529322002875</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">28</style></volume><pages><style face="normal" font="default" size="100%">100889</style></pages><isbn><style face="normal" font="default" size="100%">2542-5293</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;A fine control of carriers in solids is the most essential thing while exploring any functionality. For a ternary skutterudite like CoSn1·5Te1.5−x, which has been recently recognized as a potential material for thermoelectric conversion, the dominant carrier could be either electrons or holes via chemically tuning the quaternary Sn2Te2 rings in the structure. Both theoretical calculation and different spectroscopic probes, such as X-ray photoelectron spectroscopy (XPS) and X-ray absorption spectroscopy (XAS) were employed to unveil the conduction type switching details. On the other hand, a Ni-for-Co substitution was applied to enhance electronic transport, and thereby the thermoelectric power factor. Thanks to the substantial cut-off of lattice thermal conductivity by the characteristic Sn2Te2 rings in the skutterudite structure, ultimately a 70-fold increase in the dimensionless figure-of-merit (zT) is achieved at 723 K with the nominal composition Co0·95Ni0·05Sn1·5Te1.5.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Venugopal, Boya</style></author><author><style face="normal" font="default" size="100%">Syum, Zeru</style></author><author><style face="normal" font="default" size="100%">Yu, Sheng-Yu</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Indrajit Shown</style></author><author><style face="normal" font="default" size="100%">Chu, Chih-Wei</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Chih-Hao Lee</style></author><author><style face="normal" font="default" size="100%">Heng-Liang Wu</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhancing the Areal Capacity and Stability of Cu2ZnSnS4 Anode Materials by Carbon Coating: Mechanistic and Structural Studies During Lithiation and Delithiation</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Omega</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acsomega.1c05076</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">9152 - 9163</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">11</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;doi: 10.1021/acsomega.1c05076&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ho, Thi-Thong</style></author><author><style face="normal" font="default" size="100%">Jokar, Efat</style></author><author><style face="normal" font="default" size="100%">Quadir, Shaham</style></author><author><style face="normal" font="default" size="100%">Ruei-San Chen</style></author><author><style face="normal" font="default" size="100%">Liu, Fang-Chen</style></author><author><style face="normal" font="default" size="100%">Cheng-YingChen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhancing the photovoltaic properties of SnS-Based solar cells by crystallographic orientation engineering</style></title><secondary-title><style face="normal" font="default" size="100%">Solar Energy Materials and Solar Cells</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Crystal orientation control</style></keyword><keyword><style  face="normal" font="default" size="100%">Thin film solar cells</style></keyword><keyword><style  face="normal" font="default" size="100%">Tin monosulfide</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0927024821005389</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">236</style></volume><pages><style face="normal" font="default" size="100%">111499</style></pages><isbn><style face="normal" font="default" size="100%">0927-0248</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Tin monosulfide (SnS) is a promising light-harvesting material for solar cell applications, owing to its potential for large-scale production, cost-effectiveness, eco-friendly source materials, and long-term stability. However, SnS crystallizes in an orthorhombic structure, which results in a highly anisotropic charge transport behavior. Tailoring the crystallographic orientation of the SnS absorber layer plays a critical role in the enhancement of the transfer of charge carriers and the power conversion efficiency (PCE). By controlling the substrate tilting angle and temperature ramp rate in vapor transport deposition, the crystal growth orientation was tuned to a preferred direction which significantly suppressed the unfavorable (040) crystallographic plane. Through the combination of these two approaches, the PCE could be increased from 0.11% to 2%. The effect of the tilting angle was numerically simulated to investigate its role in controlling the film uniformity and directing the film growth. In addition, the correlation between the texture coefficient of the (040) plane and the charge transport properties was determined by a combination of analytical methods such as device performance studies, electrochemical impedance spectroscopy, along with transient photovoltage, space-charge-limited current, and dark current measurements. These techniques were blended together to prove that the marked improvement in PCE can be ascribed to a reduced charge recombination (in both SnS bulk and interfaces) and an enhanced hole mobility.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ho, Thi-Thong</style></author><author><style face="normal" font="default" size="100%">Yang, Zi-Liang</style></author><author><style face="normal" font="default" size="100%">Fang-Yu Fu</style></author><author><style face="normal" font="default" size="100%">Jokar, Efat</style></author><author><style face="normal" font="default" size="100%">Hsu, Hung-Chang</style></author><author><style face="normal" font="default" size="100%">Liu, Pei-Chi</style></author><author><style face="normal" font="default" size="100%">Quadir, Shaham</style></author><author><style face="normal" font="default" size="100%">Cheng-YingChen</style></author><author><style face="normal" font="default" size="100%">Ya-Ping Chiu</style></author><author><style face="normal" font="default" size="100%">Chih-I Wu</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Modulation and Direct Mapping of the Interfacial Band Alignment of an Eco-Friendly Zinc-Tin-Oxide Buffer Layer in SnS Solar Cells</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Applied Energy MaterialsACS Applied Energy Materials</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acsaem.2c03129</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">5</style></volume><pages><style face="normal" font="default" size="100%">14531 - 14540</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">n/a</style></abstract><issue><style face="normal" font="default" size="100%">11</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;doi: 10.1021/acsaem.2c03129&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Fang-Yu Fu</style></author><author><style face="normal" font="default" size="100%">Fan, Chi-Chan</style></author><author><style face="normal" font="default" size="100%">Mohammad Qorbani</style></author><author><style face="normal" font="default" size="100%">Huang,Chih-Yang</style></author><author><style face="normal" font="default" size="100%">Kuo, Ping-Chun</style></author><author><style face="normal" font="default" size="100%">Jih-Shang Hwang</style></author><author><style face="normal" font="default" size="100%">Shu, Guo-Jiun</style></author><author><style face="normal" font="default" size="100%">Chang, Sue-Min</style></author><author><style face="normal" font="default" size="100%">Heng-Liang Wu</style></author><author><style face="normal" font="default" size="100%">Chih-I Wu</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Selective CO2-to-CO photoreduction over an orthophosphate semiconductor via the direct Z-scheme heterojunction of Ag3PO4 quantum dots decorated on SnS2 nanosheets</style></title><secondary-title><style face="normal" font="default" size="100%">Sustainable Energy &amp; Fuels</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D2SE00873D</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">4418 - 4428</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Direct Z-scheme heterojunctions are widely used for photocatalytic water splitting and CO2 reduction due to facilitating well-separated photogenerated charge carriers and spatial isolation of redox reactions. Here, using a facile two-step hydrothermal and ion-exchange method, we uniformly decorate silver orthophosphate (i.e., Ag3PO4) quantum dots with an average characteristic size of ∼10 nm over tin(iv) sulphide (i.e., SnS2) nanosheets to form a 0D/2D heterojunction. The direct Z-scheme mechanism, i.e. charge transport for efficient electron (from SnS2) and hole (from Ag3PO4) recombination, is confirmed by the following experiments: (i) ultraviolet and X-ray photoelectron spectroscopies; (ii) photodeposition of Pt and PbO2 nanoparticles on reduction and oxidation sites, respectively; (iii) in situ X-ray photoelectron spectroscopy; and (iv) electron paramagnetic resonance spectroscopy. Owing to the photoreduction properties of Ag3PO4 with orthophosphate vacancies, Z-scheme charge carrier transfer, and efficient exciton dissociation, an optimized heterojunction shows a high CO2-to-CO reduction yield of 18.3 μmol g−1 h−1 with an illustrious selectivity of ∼95% under light illumination, which is about 3.0 and 47.8 times larger than that of Ag3PO4 and SnS2, respectively. The carbon source for the CO product is verified using a 13CO2 isotopic experiment. Moreover, by tracing the peak at ∼1190 cm−1 in the dark and under light irradiation, in situ diffuse reflectance infrared Fourier transform spectroscopy demonstrates that the CO2 reduction pathway goes through the COOH* intermediate.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">19</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Quadir, Shaham</style></author><author><style face="normal" font="default" size="100%">Mohammad Qorbani</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Wu, Tai-Sing</style></author><author><style face="normal" font="default" size="100%">Anbalagan, Aswin kumar</style></author><author><style face="normal" font="default" size="100%">Chen, Wei-Tin</style></author><author><style face="normal" font="default" size="100%">Valiyaveettil, Suneesh Meledath</style></author><author><style face="normal" font="default" size="100%">Thong, Ho-Thi</style></author><author><style face="normal" font="default" size="100%">Wang, Chin-Wei</style></author><author><style face="normal" font="default" size="100%">Cheng-YingChen</style></author><author><style face="normal" font="default" size="100%">Chih-Hao Lee</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Short- and Long-Range Cation Disorder in (AgxCu1–x)2ZnSnSe4 Kesterites</style></title><secondary-title><style face="normal" font="default" size="100%">Chemistry of Materials</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acs.chemmater.2c01489</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><isbn><style face="normal" font="default" size="100%">0897-4756</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;doi: 10.1021/acs.chemmater.2c01489&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Yang, Min-Jung</style></author><author><style face="normal" font="default" size="100%">Yusuf Fakhri, Muhammad</style></author><author><style face="normal" font="default" size="100%">Liao, Chien-Neng</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis and characterization of Ge-Ag-Sb-S-Se-Te high-entropy thermoelectric alloys</style></title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Functional</style></keyword><keyword><style  face="normal" font="default" size="100%">High-entropy alloy</style></keyword><keyword><style  face="normal" font="default" size="100%">Lattice distortion</style></keyword><keyword><style  face="normal" font="default" size="100%">Phase transformation</style></keyword><keyword><style  face="normal" font="default" size="100%">Thermal properties</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0167577X21023168</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">311</style></volume><pages><style face="normal" font="default" size="100%">131617</style></pages><isbn><style face="normal" font="default" size="100%">0167-577X</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Multielement alloying is an appealing approach for suppressing thermal conductivity of thermoelectric materials. In this study, we synthesized GeTe-based high-entropy alloys with notable (S, Se) substitution at Te sites and (Ag, Sb) at Ge sites. The Ge0.82Ag0.08Sb0.1S0.5Se0.1Te0.4 exhibits an extremely low thermal conductivity of ∼ 0.66 W/m⋅K and a high Seebeck coefficient (&amp;gt;250 μV/K) over a temperature range of 150 – 400 °C. The influence of lattice distortion on phase transformation and transport properties of Ge0.9-2xAg2xSb0.1S0.5Se0.1Te0.4 (x = 0 – 0.06) was investigated.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Fathabadi, Milad</style></author><author><style face="normal" font="default" size="100%">Mohammad Qorbani</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Quadir, Shaham</style></author><author><style face="normal" font="default" size="100%">Huang,Chih-Yang</style></author><author><style face="normal" font="default" size="100%">Chen, Kuei Hsien</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Naimeh Naseri</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ultrathin amorphous defective co-doped hematite passivation layer derived via in-situ electrochemical method for durable photoelectrochemical water oxidation</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D2TA03792K</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><pages><style face="normal" font="default" size="100%"> - </style></pages><isbn><style face="normal" font="default" size="100%">2050-7488</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Although hematite (i.e., α-Fe2O3) has been widely investigated in photoelectrochemical water oxidation studies due to its high theoretical photocurrent density, it still suffers from serious surface charge recombination and low photoelectrochemical stability. Here we report an in-situ electrochemical method to form a uniform and ultrathin (i.e., 3–5 nm) passivation layer all over the porosities of the optimized ~3.2% Ti-doped α-Fe2O3 photoanode. We unveil the amorphous and defective nature of the in-situ derived layer assigning to a high concentration of oxygen vacancy and intercalated potassium atoms there, i.e., the formation of Ti/K co-doped defective α-Fe2O3-x. Owing to the efficient passivation of surface states, alleviated surface-potential fluctuations, and low charge-transfer resistance at the interface, photoanodes show an average of ~60% enhancement in the photoelectrochemical performance, applied bias absorbed photon-to-current efficiency of 0.43%, and Faradaic efficiency of ~88%. Moreover, the passivation layer prevents direct contact between the electrode material and electrolyte, resulting in less degradation and outstanding photoelectrochemical stability with photocurrent retention of ~95% after ~100 hours, albeit by performing several successive in-situ electrochemical passivation processes. This work presents an industrially scalable method to controllably engineer the interfaces of semiconductors–electrolytes with precious metal-free defective hematite-based co-catalysts for sustainable photoelectrochemical solar-to-fuel conversion applications.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shelke, Abhijeet R.</style></author><author><style face="normal" font="default" size="100%">Wang, Hsiao-Tsu</style></author><author><style face="normal" font="default" size="100%">Chiou, Jau-Wern</style></author><author><style face="normal" font="default" size="100%">Indrajit Shown</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Chen, Kuang-Hung</style></author><author><style face="normal" font="default" size="100%">Teng, Shu-Ang</style></author><author><style face="normal" font="default" size="100%">Lin, I-An</style></author><author><style face="normal" font="default" size="100%">Lee, Chi-Cheng</style></author><author><style face="normal" font="default" size="100%">Hsueh, Hung-Chung</style></author><author><style face="normal" font="default" size="100%">Liang, Yu-Hui</style></author><author><style face="normal" font="default" size="100%">Du, Chao-Hung</style></author><author><style face="normal" font="default" size="100%">Yadav, Priyanka L.</style></author><author><style face="normal" font="default" size="100%">Ray, Sekhar C.</style></author><author><style face="normal" font="default" size="100%">Hsieh, Shang-Hsien</style></author><author><style face="normal" font="default" size="100%">Pao, Chih-Wen</style></author><author><style face="normal" font="default" size="100%">Tsai, Huang-Ming</style></author><author><style face="normal" font="default" size="100%">Chen, Chia-Hao</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Pong, Way-Faung</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Bandgap Shrinkage and Charge Transfer in 2D Layered SnS2 Doped with V for Photocatalytic Efficiency Improvement</style></title><secondary-title><style face="normal" font="default" size="100%">Small</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">band-gap shrinkage</style></keyword><keyword><style  face="normal" font="default" size="100%">charge transfer</style></keyword><keyword><style  face="normal" font="default" size="100%">Density functional theory</style></keyword><keyword><style  face="normal" font="default" size="100%">resonant inelastic X-ray scattering</style></keyword><keyword><style  face="normal" font="default" size="100%">V-doped 2D layered SnS2</style></keyword><keyword><style  face="normal" font="default" size="100%">X-ray absorption</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/abs/10.1002/smll.202105076</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">n/a</style></number><volume><style face="normal" font="default" size="100%">n/a</style></volume><pages><style face="normal" font="default" size="100%">2105076</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Abstract Effects of electronic and atomic structures of V-doped 2D layered SnS2 are studied using X-ray spectroscopy for the development of photocatalytic/photovoltaic applications. Extended X-ray absorption fine structure measurements at V K-edge reveal the presence of VO and VS bonds which form the intercalation of tetrahedral OVS sites in the van der Waals (vdW) gap of SnS2 layers. X-ray absorption near-edge structure (XANES) reveals not only valence state of V dopant in SnS2 is ≈4+ but also the charge transfer (CT) from V to ligands, supported by V Lα,β resonant inelastic X-ray scattering. These results suggest V doping produces extra interlayer covalent interactions and additional conducting channels, which increase the electronic conductivity and CT. This gives rapid transport of photo-excited electrons and effective carrier separation in layered SnS2. Additionally, valence-band photoemission spectra and S K-edge XANES indicate that the density of states near/at valence-band maximum is shifted to lower binding energy in V-doped SnS2 compare to pristine SnS2 and exhibits band gap shrinkage. These findings support first-principles density functional theory calculations of the interstitially tetrahedral OVS site intercalated in the vdW gap, highlighting the CT from V to ligands in V-doped SnS2.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Noppanut Daichakomphu</style></author><author><style face="normal" font="default" size="100%">Suman Abbas</style></author><author><style face="normal" font="default" size="100%">Chou, Ta-Lei</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Aparporn Sakulkalavek</style></author><author><style face="normal" font="default" size="100%">Rachsak Sakdanuphab</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Understanding the effect of sputtering pressures on the thermoelectric properties of GeTe films</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Alloys and Compounds</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">GeTe film</style></keyword><keyword><style  face="normal" font="default" size="100%">RF magnetron sputtering</style></keyword><keyword><style  face="normal" font="default" size="100%">Thermoelectric</style></keyword><keyword><style  face="normal" font="default" size="100%">Working pressure</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S092583882103752X</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">893</style></volume><pages><style face="normal" font="default" size="100%">162342</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;In this work, we study the effect of sputtering pressures on the thermoelectric properties of GeTe films. The working pressures were differentiated from 3 to 30 mTorr, and the as-deposited films were annealed at 623 K for 10 min in Ar atmosphere. The results show that the working pressure has a significant effect on the Ge content and crystalline size. The turning trend of the Seebeck coefficient with different sputtering pressures corresponds to the Ge content. The surface morphology of annealed film will change from cracks to voids with increasing sputtering pressure. This behavior can be explained by the growth mechanisms model. The voids and relatively low crystalline size of GeTe films affect to the reduction of the electrical conductivity. In addition, the void content decreased as film thickness was increased. Therefore, controlling the working pressures in the sputtering process and film thickness is important for the thermoelectric performance of GeTe thin film. In our work, we prove that the thermoelectric properties of GeTe films could be optimized effectively by simply tuning different sputtering conditions.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Syum, Zeru</style></author><author><style face="normal" font="default" size="100%">Tadesse Billo</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Venugopal, Boya</style></author><author><style face="normal" font="default" size="100%">Yu, Sheng-Yu</style></author><author><style face="normal" font="default" size="100%">Fang-Yu Fu</style></author><author><style face="normal" font="default" size="100%">Heng-Liang Wu</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Copper Zinc Tin Sulfide Anode Materials for Lithium-Ion Batteries at Low Temperature</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Sustainable Chemistry &amp; EngineeringACS Sustainable Chemistry &amp; Engineering</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2021</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acssuschemeng.1c01341</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">n/a</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;doi: 10.1021/acssuschemeng.1c01341&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sabhapathy, Palani</style></author><author><style face="normal" font="default" size="100%">Indrajit Shown</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Putikam Raghunath</style></author><author><style face="normal" font="default" size="100%">Chen, Jeng-Lung</style></author><author><style face="normal" font="default" size="100%">Wei-Fu Chen</style></author><author><style face="normal" font="default" size="100%">Lin, Ming-Chang</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Electronic structure modulation of isolated Co-N4 electrocatalyst by sulfur for improved pH-universal hydrogen evolution reaction</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Atomic cobalt</style></keyword><keyword><style  face="normal" font="default" size="100%">ELECTRONIC STRUCTURE</style></keyword><keyword><style  face="normal" font="default" size="100%">graphene</style></keyword><keyword><style  face="normal" font="default" size="100%">Hydrogen evolution reaction (HER)</style></keyword><keyword><style  face="normal" font="default" size="100%">Nitrogen and sulfur co-doped</style></keyword><keyword><style  face="normal" font="default" size="100%">Nonprecious electrocatalyst</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2021</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S2211285520311186</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">80</style></volume><pages><style face="normal" font="default" size="100%">105544</style></pages><isbn><style face="normal" font="default" size="100%">2211-2855</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Exploring an efficient platinum group metal (PGM) free electrocatalyst with superior activity and stability for hydrogen evolution reaction (HER) in a wide pH range is desirable for low-cost hydrogen production. Here, we report atomically dispersed cobalt on nitrogen and sulfur co-doped graphene (N-Co-S/G) for HER. Remarkably, the prepared N-Co-S/G electrocatalyst shows a small overpotential of 67.7 mV vs. reversible hydrogen electrode (RHE) at a current density of 10 mA cm−2 and exceptional durability over 100 h at 10 mA cm−2 under acidic conditions. Moreover, we found that the HER activity of N-Co-S/G is close to 20% Pt/C at all pH levels (0–14) and superior activity at high current density (&amp;gt;100 mA cm−2). Experimental and theoretical calculations reveal that the S atom in N-Co-S/G form Co-S bond, resulting new Co-N3S1 active site, which optimizes Gibbs free energy for hydrogen adsorption (∆GH*) close to zero, while water adsorption and dissociation enhanced by S modulation for neutral and basic media HER.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Thang, Nguyen Quoc</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Thi, Cao Minh</style></author><author><style face="normal" font="default" size="100%">Viet, Pham Van</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">High-efficient photocatalytic degradation of commercial drugs for pharmaceutical wastewater treatment prospects: A case study of Ag/g-C3N4/ZnO nanocomposite materials</style></title><secondary-title><style face="normal" font="default" size="100%">Chemosphere</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Ag/g-CN/ZnO nanorods</style></keyword><keyword><style  face="normal" font="default" size="100%">Catalyst dose</style></keyword><keyword><style  face="normal" font="default" size="100%">Commercial pharmaceuticals</style></keyword><keyword><style  face="normal" font="default" size="100%">Photocatalytic degradation</style></keyword><keyword><style  face="normal" font="default" size="100%">Visible light</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2021</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0045653521014430</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">282</style></volume><pages><style face="normal" font="default" size="100%">130971</style></pages><isbn><style face="normal" font="default" size="100%">0045-6535</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Pharmaceutical drugs' removal from wastewater by photocatalytic oxidation process is considered as an attractive approach and environmentally friendly solution. This report aims to appraise the practical application potential of Ag/g-C3N4/ZnO nanorods toward the wastewater treatment of the pharmaceutical industry. The catalysts are synthesized by straightforward and environmentally-friendly strategies. Specifically, g-C3N4/ZnO nanorods heterostructure is constructed by a simple self-assembly method, and then Ag nanoparticles are decorated on g-C3N4/ZnO nanorods by a photoreduction route. The results show that three commercial drugs (paracetamol, amoxicillin, and cefalexin) with high concentration (40 mg L−1) are significantly degraded in the existence of a small dosage of Ag/g-C3N4/ZnO nanorods (0.08 g L−1). The Ag/g-C3N4/ZnO nanorods photocatalyst exhibits degradation performance of paracetamol higher 3.8, 1.8, 1.3 times than pristine g-C3N4, ZnO nanorods, and g-C3N4/ZnO nanorods. Furthermore, Ag/g-C3N4/ZnO nanorods have an excellent reusability and a chemical stability that achieved paracetamol degradation efficiency of 78% and remained chemical structure of the photocatalyst after five cycles. In addition, the photocatalytic mechanism explanation and comparison of photocatalytic drugs’ degradation ability have also been discussed in this study.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Quadir, Shaham</style></author><author><style face="normal" font="default" size="100%">Mohammad Qorbani</style></author><author><style face="normal" font="default" size="100%">Lai, Ying-Ren</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Thong, Ho–Thi</style></author><author><style face="normal" font="default" size="100%">Hayashi, Michitoshi</style></author><author><style face="normal" font="default" size="100%">Chen, Cheng–Ying</style></author><author><style face="normal" font="default" size="100%">Chen, Kuei–Hsien</style></author><author><style face="normal" font="default" size="100%">Chen, Li–Chyong</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Impact of Cation Substitution in (AgxCu1−x)2ZnSnSe4 Absorber-Based Solar Cells toward 10% Efficiency: Experimental and Theoretical Analyses</style></title><secondary-title><style face="normal" font="default" size="100%">Solar RRLSolar RRL</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Ag–CZTSe</style></keyword><keyword><style  face="normal" font="default" size="100%">DEFECTS</style></keyword><keyword><style  face="normal" font="default" size="100%">Kesterite</style></keyword><keyword><style  face="normal" font="default" size="100%">photoluminescence</style></keyword><keyword><style  face="normal" font="default" size="100%">photovoltaics</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2021</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/solr.202100441</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><volume><style face="normal" font="default" size="100%">n/a</style></volume><pages><style face="normal" font="default" size="100%">2100441</style></pages><isbn><style face="normal" font="default" size="100%">2367-198X</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Solar cells based on kesterite Cu2ZnSnSe4 (CZTSe) compounds with earth-abundant elements are highly desirable for the low-cost and high-efficiency production of renewable energy. However, the occurrence of intrinsic defects substantially impairs the photovoltaic properties of CZTSe. Herein, a cation substitution method to control and passivate the defect states in bandgap of kesterite CZTSe by incorporating Ag ions is introduced. Intensity-dependent low-temperature photoluminescence measurements show that Ag incorporation can reduce the density and depth of intrinsic defects in CZTSe. The results reveal that 10% Ag-alloyed CZTSe provides the shallowest defect states and less nonradiative recombination. It is also confirmed by first-principles calculations that Ag incorporation enables the formation and suppresses the beneficial and detrimental defects, respectively. Based on the theoretical results, the observed subband photoluminescence peaks can be assigned to the intrinsic point and cluster defects. The best power conversion efficiency of 10.2% is achieved for the 10% Ag-alloyed CZTSe cell, along with an enhanced open-circuit voltage. These results open up a new avenue for further improving the performances of CZTSe-based device via defect engineering.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">n/a</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;&lt;a href=&quot;https://doi.org/10.1002/solr.202100441&quot;&gt;https://doi.org/10.1002/solr.202100441&lt;/a&gt;&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kamal Hussien, Mahmoud</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Mohammad Qorbani</style></author><author><style face="normal" font="default" size="100%">Hammad Elsayed, Mohamed</style></author><author><style face="normal" font="default" size="100%">Putikam Raghunath</style></author><author><style face="normal" font="default" size="100%">Lin, Tsai-Yu</style></author><author><style face="normal" font="default" size="100%">Quadir, Shaham</style></author><author><style face="normal" font="default" size="100%">Wang, Hong-Yi</style></author><author><style face="normal" font="default" size="100%">Heng-Liang Wu</style></author><author><style face="normal" font="default" size="100%">Tzou, Der-Lii M.</style></author><author><style face="normal" font="default" size="100%">Lin, Ming-Chang</style></author><author><style face="normal" font="default" size="100%">Chung, Po-Wen</style></author><author><style face="normal" font="default" size="100%">Chou, Ho-Hsiu</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Metal-free four-in-one modification of g-C3N4 for superior photocatalytic CO2 reduction and H2 evolution</style></title><secondary-title><style face="normal" font="default" size="100%">Chemical Engineering Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">g-CN, CO reduction</style></keyword><keyword><style  face="normal" font="default" size="100%">Gas bubble template</style></keyword><keyword><style  face="normal" font="default" size="100%">Hydrogen generation</style></keyword><keyword><style  face="normal" font="default" size="100%">Metal-free photocatalyst</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2021</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S1385894721044284</style></url></web-urls></urls><pages><style face="normal" font="default" size="100%">132853</style></pages><isbn><style face="normal" font="default" size="100%">1385-8947</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Utilization of g-C3N4 as a single photocatalyst material without combination with other semiconductor remains challenging. Herein, we report a facile green method for synthesizing a metal free modified g-C3N4 photocatalyst. The modification process combines four different strategies in a one-pot thermal reaction: non-metal doping, porosity generation, functionalization with amino groups, and thermal oxidation etching. The as-prepared amino-functionalized ultrathin nanoporous boron-doped g-C3N4 exhibited a high specific surface area of 143.2 m2 g−1 which resulted in abundant adsorption sites for CO2 and water molecules. The surface amino groups act as Lewis basic sites to adsorb acidic CO2 molecules, which can also serve as active sites to facilitate hydrogen generation. Besides, the simultaneous use of ammonium chloride as a dynamic gas bubble template along with thermal oxidation etching efficiently boosts the delamination of the g-C3N4 layers to produce ultrathin sheets; this leads to stronger light–matter interactions and efficient charge generation. Consequently, the newly modified g-C3N4 achieved selective gas-phase CO2 reduction into CO with a production yield of 21.95 µmol g-1, in the absence of any cocatalyst. Moreover, a high hydrogen generation rate of 3800 µmol g-1 h-1 and prominent apparent quantum yield of 10.6% were recorded. This work opens up a new avenue to explore different rational modifications of g-C3N4 nanosheets for the efficient production of clean energy.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Venugopal, Boya</style></author><author><style face="normal" font="default" size="100%">Indrajit Shown</style></author><author><style face="normal" font="default" size="100%">Satyanarayana Samireddi</style></author><author><style face="normal" font="default" size="100%">Syum, Zeru</style></author><author><style face="normal" font="default" size="100%">Krishnamoorthy, Vimal</style></author><author><style face="normal" font="default" size="100%">Heng-Liang Wu</style></author><author><style face="normal" font="default" size="100%">Chu, Chih-Wei</style></author><author><style face="normal" font="default" size="100%">Chih-Hao Lee</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Microstructural intra-granular cracking in Cu2ZnSnS4@C thin-film anode enhanced the electrochemical performance in lithium-ion battery applications</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Advances</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2021</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D1MA00471A</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">RSC</style></publisher><volume><style face="normal" font="default" size="100%">2</style></volume><pages><style face="normal" font="default" size="100%">5672 - 5685</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Cu2ZnSnS4 (CZTS) has demonstrated excellent performance as an anode material for lithium-ion batteries. However, the repeated lithiation and delithiation create a cracking pattern and lead to island formation in the thin-film electrode, resulting in a capacity fading over cycling in lithium-ion batteries (LIB's). In order to control this crack behaviour, we introduce carbon into CZTS thin-films by a hydrothermal method to form CZTS@C composite. CZTS@C significantly reduced the crack pattern formation on the electrode surface as well as improved the conductivity of the CZTS@C electrode. At the early stages of lithiation and delithiation, the volume expansion and contraction of Li–CZTS@C create intra-granular cracking only at the surface level, and it offers a high capacity of about 785 mA h g−1 after 150 cycles at 1000 mA g−1 charging rate, excellent rate capability (942 mA h g−1, 678 mA h g−1 and 435 mA h g−1 at 500 mA g−1, 2000 mA g−1 and 5000 mA g−1), and superior cyclability (925 mA h g−1 even after 200 cycles at 500 mA g−1). The excellent electrochemical performance at high-current rates can be attributed to intra-granular cracking together with carbon coating that provides a short transportation length for both lithium ions and electrons. Moreover, the controlled cracking pattern formation in CZTS@C facilitates faster reaction kinetics, which open up a new solution for the development of high-power thin-film anodes for next-generation LIBs applications.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">17</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">He-Yun Du</style></author><author><style face="normal" font="default" size="100%">Yi-Fan Huang</style></author><author><style face="normal" font="default" size="100%">Wong, Deniz</style></author><author><style face="normal" font="default" size="100%">Tseng, Mao-Feng</style></author><author><style face="normal" font="default" size="100%">Yi-Hsin Lee</style></author><author><style face="normal" font="default" size="100%">Chen-Hao Wang</style></author><author><style face="normal" font="default" size="100%">Lin, Cheng-Lan</style></author><author><style face="normal" font="default" size="100%">Hoffmann, Germar</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nanoscale redox mapping at the MoS2-liquid interface</style></title></titles><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2021</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1038/s41467-021-21660-z</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">1321</style></pages><isbn><style face="normal" font="default" size="100%">2041-1723</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Layered MoS2 is considered as one of the most promising two-dimensional photocatalytic materials for hydrogen evolution and water splitting; however, the electronic structure at the MoS2-liquid interface is so far insufficiently resolved. Measuring and understanding the band offset at the surfaces of MoS2 are crucial for understanding catalytic reactions and to achieve further improvements in performance. Herein, the heterogeneous charge transfer behavior of MoS2 flakes of various layer numbers and sizes is addressed with high spatial resolution in organic solutions using the ferrocene/ferrocenium (Fc/Fc+) redox pair as a probe in near-field scanning electrochemical microscopy, i.e. in close nm probe-sample proximity. Redox mapping reveals an area and layer dependent reactivity for MoS2 with a detailed insight into the local processes as band offset and confinement of the faradaic current obtained. In combination with additional characterization methods, we deduce a band alignment occurring at the liquid-solid interface.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shih-Wei Lee</style></author><author><style face="normal" font="default" size="100%">Abdi, Zelalem Gudeta</style></author><author><style face="normal" font="default" size="100%">Jyh-Chien Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Optimal method for preparing sulfonated polyaryletherketones with high ion exchange capacity by acid-catalyzed crosslinking for proton exchange membrane fuel cells</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Polymer ScienceJournal of Polymer Science</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Fuel cell</style></keyword><keyword><style  face="normal" font="default" size="100%">Proton exchange membrane</style></keyword><keyword><style  face="normal" font="default" size="100%">sulfonated poly(aryletherketone)</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2021</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/pol.20200872</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><volume><style face="normal" font="default" size="100%">59</style></volume><pages><style face="normal" font="default" size="100%">706 - 720</style></pages><isbn><style face="normal" font="default" size="100%">2642-4150</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Abstract Sulfonated polyaryletherketones (SPAEK) bearing four sulfonic acid groups on the phenyl side groups were synthesized. The benzophenone moiety of polymer backbone was further reduced to benzydrol group with sodium borohydride. The membranes were crosslinked by acid-catalyzed Friedel-Crafts reaction without sacrifice of sulfonic acid groups and ion exchange capacity (IEC) values. Crosslinked membranes with the same IEC value but different water uptake could be prepared. The optimal crosslinking condition was investigated to achieve lower water uptake, better chemical stability (Fenton's test), and higher proton conductivity. In addition, the hydrophilic ionic channels from originally course and disordered could be modified to be narrow and continuous by this crosslinking method. The crosslinked membranes, CS4PH-40-PEKOH (IEC = 2.4 meq./g), reduced water uptake from 200 to 88% and the weight loss was reduced from 11 to 5% during the Fenton test compared to uncrosslinked one (S4PH-40-PEK). The membrane showed comparable proton conductivity (0.01?0.19?S/cm) to Nafion 212 at 80°C from low to high relative humidity (RH). Single H2/O2 fuel cell based on the crosslinked SPAEK with catalyst loading of 0.25?mg/cm2 (Pd/C) exhibited a peak power density of 220.3 mW/cm2, which was close to that of Nafion 212 (214.0 mW/cm2) at 80°C under 53% RH. These membranes provide a good option as proton exchange membrane with high ion exchange capacity for fuel cells.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">8</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;&lt;a href=&quot;https://doi.org/10.1002/pol.20200872&quot;&gt;https://doi.org/10.1002/pol.20200872&lt;/a&gt;&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hsiang-Ting Lien</style></author><author><style face="normal" font="default" size="100%">Chang, Yu-Chung</style></author><author><style face="normal" font="default" size="100%">Huang,Chih-Yang</style></author><author><style face="normal" font="default" size="100%">Hsin-Cheng Hsu</style></author><author><style face="normal" font="default" size="100%">Sun-Tang Chang</style></author><author><style face="normal" font="default" size="100%">Deniz P. Wong</style></author><author><style face="normal" font="default" size="100%">Wang,Chia-Hsin</style></author><author><style face="normal" font="default" size="100%">Chen-Hao Wang</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Solar to hydrocarbon production using metal-free water-soluble bulk heterojunction of conducting polymer nanoparticle and graphene oxide</style></title><secondary-title><style face="normal" font="default" size="100%">The Journal of Chemical PhysicsThe Journal of Chemical Physics</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2021</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1063/5.0042716</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Institute of Physics</style></publisher><volume><style face="normal" font="default" size="100%">154</style></volume><pages><style face="normal" font="default" size="100%">164707</style></pages><isbn><style face="normal" font="default" size="100%">0021-9606</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">n/a</style></abstract><issue><style face="normal" font="default" size="100%">16</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;doi: 10.1063/5.0042716&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Syum, Zeru</style></author><author><style face="normal" font="default" size="100%">Venugopal, Boya</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Tadesse Billo</style></author><author><style face="normal" font="default" size="100%">Tsu-chin Chou</style></author><author><style face="normal" font="default" size="100%">Heng-Liang Wu</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Superior lithium-ion storage performance of hierarchical tin disulfide and carbon nanotube-carbon cloth composites</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Power Sources</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Conductive supports</style></keyword><keyword><style  face="normal" font="default" size="100%">Hierarchical carbon composites</style></keyword><keyword><style  face="normal" font="default" size="100%">Lithium ion batteries</style></keyword><keyword><style  face="normal" font="default" size="100%">Tin disulfide</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2021</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0378775320312246</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">482</style></volume><pages><style face="normal" font="default" size="100%">228923</style></pages><isbn><style face="normal" font="default" size="100%">0378-7753</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Tin-based composites are promising anode materials for high-performance lithium-ion batteries (LIBs); however, insufficient conductivity, as well as fatal volume expansion during cycling lead to poor electrochemical reversibility and cycling stability. In this work, we demonstrate the lithium-ion storage behaviors of SnS2 anode material deposited on different electrode supports. The SnS2 grown on 3D hierarchical carbon nanotube-carbon cloth composites (SnS2-CNT-CC) shows superior capacity retention and cycle stability, compared to that on planar Mo sheets and carbon cloth. The specific capacity of SnS2 on Mo, CC, and CNT-CC is around 240, 840, and 1250 g−1, respectively. The SnS2-CNT-CC electrode outperforms in the cyclic performance and rate capability compared to other electrode configurations due to the multi-electron pathway and high surface area derived from 3D hierarchical CNT-CC electrode support. Furthermore, a significant decrease in the charge transfer resistance is observed by utilizing 3D hierarchical CNT-CC electrode support. The use of 3D hierarchical structures as electrode support could be the best alternative to enhance the electrochemical performances for the next generation LIBs.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Su, Teng-Yu</style></author><author><style face="normal" font="default" size="100%">Wang, Te-Hsien</style></author><author><style face="normal" font="default" size="100%">Deniz P. Wong</style></author><author><style face="normal" font="default" size="100%">Wang, Yi-Chung</style></author><author><style face="normal" font="default" size="100%">Huang, Angus</style></author><author><style face="normal" font="default" size="100%">Sheng, Ying-Chun</style></author><author><style face="normal" font="default" size="100%">Tang, Shin-Yi</style></author><author><style face="normal" font="default" size="100%">Tsu-chin Chou</style></author><author><style face="normal" font="default" size="100%">Chou, Ta-Lei</style></author><author><style face="normal" font="default" size="100%">Jeng, Horng-Tay</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Chueh, Yu-Lun</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Thermally Strain-Induced Band Gap Opening on Platinum Diselenide-Layered Films: A Promising Two-Dimensional Material with Excellent Thermoelectric Performance</style></title><secondary-title><style face="normal" font="default" size="100%">Chemistry of MaterialsChemistry of Materials</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2021</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acs.chemmater.0c04351</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">33</style></volume><pages><style face="normal" font="default" size="100%">3490 - 3498</style></pages><isbn><style face="normal" font="default" size="100%">0897-4756</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">n/a</style></abstract><issue><style face="normal" font="default" size="100%">10</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;doi: 10.1021/acs.chemmater.0c04351&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Satyanarayana Samireddi</style></author><author><style face="normal" font="default" size="100%">Aishwarya, V.</style></author><author><style face="normal" font="default" size="100%">Indrajit Shown</style></author><author><style face="normal" font="default" size="100%">Muthusamy, Saravanakumar</style></author><author><style face="normal" font="default" size="100%">Unni, Sreekuttan M.</style></author><author><style face="normal" font="default" size="100%">Ken-Tsung Wong</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synergistic Dual-Atom Molecular Catalyst Derived from Low-Temperature Pyrolyzed Heterobimetallic Macrocycle-N4 Corrole Complex for Oxygen Reduction</style></title><secondary-title><style face="normal" font="default" size="100%">Small</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">corroles</style></keyword><keyword><style  face="normal" font="default" size="100%">dual-atom molecular catalyst</style></keyword><keyword><style  face="normal" font="default" size="100%">fuel cells</style></keyword><keyword><style  face="normal" font="default" size="100%">metal–N4 macrocycles</style></keyword><keyword><style  face="normal" font="default" size="100%">non-precious electrocatalysts</style></keyword><keyword><style  face="normal" font="default" size="100%">oxygen reduction reaction</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/abs/10.1002/smll.202103823</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">46</style></number><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">2103823</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Abstract A heterobimetallic corrole complex, comprising oxygen reduction reaction (ORR) active non-precious metals Co and Fe with a corrole-N4 center (PhFCC), is successfully synthesized and used to prepare a dual-atom molecular catalyst (DAMC) through subsequent low-temperature pyrolysis. This low-temperature pyrolyzed electrocatalyst exhibited impressive ORR performance, with onset potentials of 0.86 and 0.94 V, and half-wave potentials of 0.75 and 0.85 V, under acidic and basic conditions, respectively. During potential cycling, this DAMC displayed half-wave potential losses of only 25 and 5 mV under acidic and alkaline conditions after 3000 cycles, respectively, demonstrating its excellent stability. Single-cell Nafion-based proton exchange membrane fuel cell performance using this DAMC as the cathode catalyst showed a maximum power density of 225 mW cm−2, almost close to that of most metal–N4 macrocycle-based catalysts. The present study showed that preservation of the defined CoN4 structure along with the cocatalytic Fe–Cx site synergistically acted as a dual ORR active center to boost overall ORR performance. The development of DAMC from a heterobimetallic CoN4-macrocyclic system using low-temperature pyrolysis is also advantageous for practical applications.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Yi-Fan Huang</style></author><author><style face="normal" font="default" size="100%">Liao, Kuan-Wei</style></author><author><style face="normal" font="default" size="100%">Fahmi, Fariz Rifqi Zul</style></author><author><style face="normal" font="default" size="100%">Modak, Varad A.</style></author><author><style face="normal" font="default" size="100%">Tsai, Shang-Hsuan</style></author><author><style face="normal" font="default" size="100%">Ke, Shang-Wei</style></author><author><style face="normal" font="default" size="100%">Chen-Hao Wang</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Thickness-Dependent Photocatalysis of Ultra-Thin MoS2 Film for Visible-Light-Driven CO2 Reduction</style></title><secondary-title><style face="normal" font="default" size="100%">Catalysts</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2021</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.mdpi.com/2073-4344/11/11/1295</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">11</style></number><volume><style face="normal" font="default" size="100%">11</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The thickness of transition metal dichalcogenides (TMDs) plays a key role in enhancing their photocatalytic CO2 reduction activity. However, the optimum thickness of the layered TMDs that is required to achieve sufficient light absorption and excellent crystallinity has still not been definitively determined. In this work, ultra-thin molybdenum disulfide films (MoS2TF) with 25 nm thickness presented remarkable photocatalytic activity, and the product yield increased by about 2.3 times. The photocatalytic mechanism corresponding to the TMDs’ thickness was also proposed. This work demonstrates that the thickness optimization of TMDs provides a cogent direction for the design of high-performance photocatalysts.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Huang, Song-Jeng</style></author><author><style face="normal" font="default" size="100%">Muneeb, Adil</style></author><author><style face="normal" font="default" size="100%">Sabhapathy, Palani</style></author><author><style face="normal" font="default" size="100%">Bayikadi, Khasim Saheb</style></author><author><style face="normal" font="default" size="100%">Murtaza, Tahir</style></author><author><style face="normal" font="default" size="100%">Raju, Kalaivanan</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Raman Sankar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Two-Dimensional Layered NiLiP2S6 Crystals as an Efficient Bifunctional Electrocatalyst for Overall Water Splitting</style></title><secondary-title><style face="normal" font="default" size="100%">Catalysts</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2021</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.mdpi.com/2073-4344/11/7/786</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">7</style></number><volume><style face="normal" font="default" size="100%">11</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The quest of earth-abundant bifunctional electrocatalysts for highly efficient oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is essential for clean and renewable energy systems. Herein, directed by the experimental analysis, we demonstrate layered nickel lithium phosphosulfide (NiLiP2S6) crystal as a highly efficient water-splitting catalyst in alkaline media. With strained lattice due to stacked layers as observed by TEM and electronic structure analysis performed by XPS showed mixed Ni2+,3+ oxidation states induced by addition of Li as a cation, NiLiP2S6 displays excellent OER (current density of 10 mA cm–2 showed an overpotential of 303 mV vs. RHE and a Tafel slope of 114 mV dec–1) and HER activity (current density of −10 mA cm–2 showed an overpotential of 184 mV vs. RHE and a Tafel slope of 94.5 mV dec–1). Finally, an alkaline media was employed to demonstrate the overall water splitting using NiLiP2S6 as both the anode and the cathode, which attained a 50 mA cm−2 current density at 1.68 V. This bimetallic phosphosulfide, together with long-term stability and enhanced intrinsic activity, shows enormous potential in water splitting applications.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Yang, Jingling</style></author><author><style face="normal" font="default" size="100%">Wang, Chun-Yao</style></author><author><style face="normal" font="default" size="100%">Wang, Chun-Chieh</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Mou, Chung-Yuan</style></author><author><style face="normal" font="default" size="100%">Heng-Liang Wu</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Advanced nanoporous separators for stable lithium metal electrodeposition at ultra-high current densities in liquid electrolytes</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2020</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C9TA13778E</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">5095 - 5104</style></pages><isbn><style face="normal" font="default" size="100%">2050-7488</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Lithium metal anodes form a dendritic structure after cycling which causes an internal short circuit in flammable electrolytes and results in battery fires. Today's separators are insufficient for suppressing the formation of lithium dendrites. Herein, we report on the use of mesoporous silica thin films (MSTFs) with perpendicular nanochannels (pore size ∼5 nm) stacking on an anodic aluminum oxide (AAO) membrane as the MSTF⊥AAO separator for advancing Li metal batteries. The nanoporous MSTF⊥AAO separator with novel inorganic structures shows ultra-long term stability of Li plating/stripping in Li–Li cells at an ultra-high current density and capacity (10 mA cm−2 and 5 mA h cm−2). A significant improvement over the state-of-the-art separator is evaluated based on three performance indicators, e.g. cycle life, current density and capacity. In Li–Cu cells, the MSTF⊥AAO separator shows a coulombic efficiency of &amp;gt;99.9% at a current density of 10 mA cm−2 for more than 250 h of cycling. The separator gives improved rate capability in Li–LiFePO4 (LFP) batteries. The excellent performance of the MSTF⊥AAO separator is due to good wetting of electrolytes, straight nanopores with negative charges, uniform Li deposition and blocking the finest dendrite.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">10</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chang, Ming-Chiang</style></author><author><style face="normal" font="default" size="100%">Po-Hsun Ho</style></author><author><style face="normal" font="default" size="100%">Tseng, Mao-Feng</style></author><author><style face="normal" font="default" size="100%">Lin, Fang-Yuan</style></author><author><style face="normal" font="default" size="100%">Hou, Cheng-Hung</style></author><author><style face="normal" font="default" size="100%">Lin, I-Kuan</style></author><author><style face="normal" font="default" size="100%">Wang, Hsin</style></author><author><style face="normal" font="default" size="100%">Huang, Pin-Pin</style></author><author><style face="normal" font="default" size="100%">Chiang, Chun-Hao</style></author><author><style face="normal" font="default" size="100%">Yang, Yueh-Chiang</style></author><author><style face="normal" font="default" size="100%">Wang, I-Ta</style></author><author><style face="normal" font="default" size="100%">He-Yun Du</style></author><author><style face="normal" font="default" size="100%">Wen, Cheng-Yen</style></author><author><style face="normal" font="default" size="100%">Jing-Jong Shyue</style></author><author><style face="normal" font="default" size="100%">Chun-Wei Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Chiu, Po-Wen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Fast growth of large-grain and continuous MoS2 films through a self-capping vapor-liquid-solid method</style></title></titles><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2020</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1038/s41467-020-17517-6</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">3682</style></pages><isbn><style face="normal" font="default" size="100%">2041-1723</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Most chemical vapor deposition methods for transition metal dichalcogenides use an extremely small amount of precursor to render large single-crystal flakes, which usually causes low coverage of the materials on the substrate. In this study, a self-capping vapor-liquid-solid reaction is proposed to fabricate large-grain, continuous MoS2 films. An intermediate liquid phase-Na2Mo2O7 is formed through a eutectic reaction of MoO3 and NaF, followed by being sulfurized into MoS2. The as-formed MoS2 seeds function as a capping layer that reduces the nucleation density and promotes lateral growth. By tuning the driving force of the reaction, large mono/bilayer (1.1 mm/200 μm) flakes or full-coverage films (with a record-high average grain size of 450 μm) can be grown on centimeter-scale substrates. The field-effect transistors fabricated from the full-coverage films show high mobility (33 and 49 cm2 V−1 s−1 for the mono and bilayer regions) and on/off ratio (1 ~ 5 × 108) across a 1.5 cm × 1.5 cm region.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">H.-C. Chang</style></author><author><style face="normal" font="default" size="100%">Chen, T.-H.</style></author><author><style face="normal" font="default" size="100%">R. Sankar</style></author><author><style face="normal" font="default" size="100%">Y-J Yang</style></author><author><style face="normal" font="default" size="100%">L.-C. Chen</style></author><author><style face="normal" font="default" size="100%">K.-H. Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Highly improved thermoelectric performance of BiCuTeO achieved by decreasing the oxygen content</style></title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Electrical conductivity</style></keyword><keyword><style  face="normal" font="default" size="100%">Figure of merit</style></keyword><keyword><style  face="normal" font="default" size="100%">Hot pressing</style></keyword><keyword><style  face="normal" font="default" size="100%">Secondary phases</style></keyword><keyword><style  face="normal" font="default" size="100%">thermal conductivity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2020</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S2542529320300729</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">100248</style></pages><isbn><style face="normal" font="default" size="100%">2542-5293</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;BiCuTeO is a promising thermoelectric material owing to its intrinsically low thermal conductivity and high carrier concentration. This study investigated the influence of stoichiometric oxygen deficiencies on the thermoelectric performance of BiCuTeO. Bulk BiCuTeO1−x (0.16 ≥ x) samples were prepared by a conventional solid state reaction and pelleted by hot pressing. Synchrotron X-ray diffraction, electron probe X-ray microanalysis, scanning electron microscopy, and transmission electron microscopy characterized the samples. A maximum value of 1.06 was achieved for the dimensionless figure of merit ZT at 673 K for BiCuTeO0.88, which is approximately 49% better than the current maximal ZT value for BiCuTeO. The power factor was noticeably improved owing to increases in the electrical conductivity and Seebeck coefficient. Moreover, the optimal oxygen deficiency could introduce nanoparticles, resulting in reduced thermal conductivity. The findings will be important for the future development of metal oxide thermoelectric materials for use in practical thermoelectric devices.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shit, Subhash Chandra</style></author><author><style face="normal" font="default" size="100%">Indrajit Shown</style></author><author><style face="normal" font="default" size="100%">Paul, Ratul</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Mondal, John</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Integrated nano-architectured photocatalysts for photochemical CO2 reduction</style></title><secondary-title><style face="normal" font="default" size="100%">Nanoscale</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2020</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D0NR05884J</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">23301 - 23332</style></pages><isbn><style face="normal" font="default" size="100%">2040-3364</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Recent advances in nanotechnology, especially the development of integrated nanostructured materials, have offered unprecedented opportunities for photocatalytic CO2 reduction. Compared to bulk semiconductor photocatalysts, most of these nanostructured photocatalysts offer at least one advantage in areas such as photogenerated carrier kinetics, light absorption, and active surface area, supporting improved photochemical reaction efficiencies. In this review, we briefly cover the cutting-edge research activities in the area of integrated nanostructured catalysts for photochemical CO2 reduction, including aqueous and gas-phase reactions. Primarily explored are the basic principles of tailor-made nanostructured composite photocatalysts and how nanostructuring influences photochemical performance. Specifically, we summarize the recent developments related to integrated nanostructured materials for photocatalytic CO2 reduction, mainly in the following five categories: carbon-based nano-architectures, metal–organic frameworks, covalent-organic frameworks, conjugated porous polymers, and layered double hydroxide-based inorganic hybrids. Besides the technical aspects of nanostructure-enhanced catalytic performance in photochemical CO2 reduction, some future research trends and promising strategies are addressed.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">46</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Thang, Nguyen Quoc</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Hai, Le Viet</style></author><author><style face="normal" font="default" size="100%">Thi, Cao Minh</style></author><author><style face="normal" font="default" size="100%">Viet, Pham Van</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Localized surface plasmonic resonance role of silver nanoparticles in the enhancement of long-chain hydrocarbons of the CO2 reduction over Ag-gC3N4/ZnO nanorods photocatalysts</style></title></titles><keywords><keyword><style  face="normal" font="default" size="100%">gCN</style></keyword><keyword><style  face="normal" font="default" size="100%">Hydrocarbon selectivity</style></keyword><keyword><style  face="normal" font="default" size="100%">Photocatalytic CO reduction</style></keyword><keyword><style  face="normal" font="default" size="100%">Surface plasmonic effect</style></keyword><keyword><style  face="normal" font="default" size="100%">ZnO nanorod</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2020</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0009250920305819</style></url></web-urls></urls><pages><style face="normal" font="default" size="100%">116049</style></pages><isbn><style face="normal" font="default" size="100%">0009-2509</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The conversion of CO2 into hydrocarbon fuels via the photocatalytic reaction route is considered a potential strategy to concurrently address serious energy crisis and greenhouse gas emission problems. Nevertheless, the generation of long-chain hydrocarbon products (Cn, n ≥ 2) from the visible-light-reactive photocatalytic CO2 reduction has also been considering a contemporary challenge. Herein, we indicate that Ag nanoparticles (Ag NPs) loaded gC3N4/ZnO nanorods heterojunction (Ag-gC3N4/ZnO NRs abbreviation) has extended photoactive range and enhanced specific surface area. The combination of Ag NPs and gC3N4/ZnO NRs significantly enhances photocatalytic CO2 reduction efficiency to form the acetone product. Detail, the acetone production efficiency of Ag-gC3N4/ZnO NRs is 8.4 and 7.5 times higher than pure ZnO NRs and gC3N4/ZnO NRs at the same condition, respectively. This study represents a potential approach toward higher-energy-value hydrocarbons production and greenhouse gas emission mitigation.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tadesse Billo</style></author><author><style face="normal" font="default" size="100%">Indrajit Shown</style></author><author><style face="normal" font="default" size="100%">Anbalagan, Aswin kumar</style></author><author><style face="normal" font="default" size="100%">Effendi, Tirta Amerta</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Fang-Yu Fu</style></author><author><style face="normal" font="default" size="100%">Chu, Che-Men</style></author><author><style face="normal" font="default" size="100%">Woon, Wei-Yen</style></author><author><style face="normal" font="default" size="100%">Ruei-San Chen</style></author><author><style face="normal" font="default" size="100%">Chih-Hao Lee</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A mechanistic study of molecular CO2 interaction and adsorption on carbon implanted SnS2 thin film for photocatalytic CO2 reduction activity</style></title></titles><keywords><keyword><style  face="normal" font="default" size="100%">artificial photosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Photocatalytic CO reduction</style></keyword><keyword><style  face="normal" font="default" size="100%">SnS</style></keyword><keyword><style  face="normal" font="default" size="100%">solar fuels</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2020</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S2211285520302743</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">72</style></volume><pages><style face="normal" font="default" size="100%">104717</style></pages><isbn><style face="normal" font="default" size="100%">2211-2855</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Gas-phase photocatalytic reactions to convert carbon dioxide and water into oxygen and hydrocarbons are the foundation of life on earth. However, the efficiency of photosynthesis is relatively low (~1%), which leaves much room for artificial photosynthesis to reach the benchmark of the solar cells (&amp;gt;15%). In this work, carbon implanted SnS2 thin films (C–SnS2) were prepared to study photocatalytic activity and adsorbate-catalyst surface interactions during CO2 photoreduction. The electron density distribution in C–SnS2 and its contribution toward the photogenerated charge transfer process has been analyzed by the angle-dependent X-ray absorption near-edge structure (XANES) study. The C–SnS2 surface affinity toward the CO2 molecule was monitored by in-situ dark current and Raman spectroscopy measurements. By optimizing the dose during ion implantation, SnS2 thin film with 1 wt% carbon incorporation shows 108 times enhancement in the CO2 conversion efficiency and more than 89% product selectivity toward CH4 formation compared with the as-grown SnS2 without carbon incorporation. The improved photocatalytic activity can be ascribed to enhanced light harvesting, pronounced charge-transfer between SnS2 and carbon with improved carrier separation and the availability of highly active carbon sites that serve as favorable CO2 adsorption sites.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Howlader, Smita</style></author><author><style face="normal" font="default" size="100%">Vasudevan, R.</style></author><author><style face="normal" font="default" size="100%">Jarwal, B.</style></author><author><style face="normal" font="default" size="100%">Gupta, S.</style></author><author><style face="normal" font="default" size="100%">K.-H. Chen</style></author><author><style face="normal" font="default" size="100%">Sachdev, K.</style></author><author><style face="normal" font="default" size="100%">Banerjee, M.K.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Microstructure and mechanical stability of Bi doped Mg2Si0.4Sn0.6 thermoelectric material</style></title></titles><keywords><keyword><style  face="normal" font="default" size="100%">High energy ball milling</style></keyword><keyword><style  face="normal" font="default" size="100%">Magnesium silicide stannide</style></keyword><keyword><style  face="normal" font="default" size="100%">Mechanical properties</style></keyword><keyword><style  face="normal" font="default" size="100%">n-type MgSiSn</style></keyword><keyword><style  face="normal" font="default" size="100%">Thermoelectric properties</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2020</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0925838819341349</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">818</style></volume><pages><style face="normal" font="default" size="100%">152888</style></pages><isbn><style face="normal" font="default" size="100%">0925-8388</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Bi doped Mg2Si0.4Sn0.6 had been synthesised in a high energy ball mill followed by compaction using a sintering hot press. The structural and compositional characterization of sintered mass indicated the formation of a highly densified single-phase product. The microstructure of the hot-pressed samples had been critically assessed. Thermoelectric properties were measured between room temperature and 723 K. A decrease in electrical conductivity was found with the increase in temperature but the Seebeck coefficient showed a reverse trend justifying the attainment of degenerate semiconducting behaviour. Meanwhile, the lattice thermal conductivity was subdued to 1.5 W/mK at 623 K. However, the highest zT value of 0.8 was achieved at 723 K. Moreover, the detailed X-ray photoelectron spectroscopic analysis was carried for the determination of binding energy of the constituent elements in the experimental alloy; it also provided the correct estimation of atomic percentage of the concerned elements. The Raman spectrum revealed a shift in F2g peak with respect to that of Mg2Sn and Mg2Si in correspondence with the composition of the synthesised alloy. The synthesised alloy showed micro and nano hardness of 3.7 and 4.03 GPa respectively, which implies that good mechanical strength could be achieved in the synthesised alloy.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Huang, Wen-Fei</style></author><author><style face="normal" font="default" size="100%">Sun-Tang Chang</style></author><author><style face="normal" font="default" size="100%">Hsin-Chih Huang</style></author><author><style face="normal" font="default" size="100%">Chen-Hao Wang</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">M. C. Lin</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">On the Reduction of O2 on Cathode Surfaces of Co–Corrin and Co–Porphyrin: A Computational and Experimental Study on Their Relative Efficiencies in H2O/H2O2 Formation</style></title><secondary-title><style face="normal" font="default" size="100%">The Journal of Physical Chemistry CThe Journal of Physical Chemistry C</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2020</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acs.jpcc.0c00481</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">124</style></volume><pages><style face="normal" font="default" size="100%">4652 - 4659</style></pages><isbn><style face="normal" font="default" size="100%">1932-7447</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">n/a</style></abstract><issue><style face="normal" font="default" size="100%">8</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;doi: 10.1021/acs.jpcc.0c00481&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hsiang-Ting Lien</style></author><author><style face="normal" font="default" size="100%">Sun-Tang Chang</style></author><author><style face="normal" font="default" size="100%">Chen, Po-Tuan</style></author><author><style face="normal" font="default" size="100%">Deniz P. Wong</style></author><author><style face="normal" font="default" size="100%">Chang, Yu-Chung</style></author><author><style face="normal" font="default" size="100%">Lu, Ying-Rei</style></author><author><style face="normal" font="default" size="100%">Dong, Chung-Li</style></author><author><style face="normal" font="default" size="100%">Chen-Hao Wang</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Probing the active site in single-atom oxygen reduction catalysts via operando X-ray and electrochemical spectroscopy</style></title></titles><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2020</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1038/s41467-020-17975-y</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">4233</style></pages><isbn><style face="normal" font="default" size="100%">2041-1723</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Nonnoble metal catalysts are low-cost alternatives to Pt for the oxygen reduction reactions (ORRs), which have been studied for various applications in electrocatalytic systems. Among them, transition metal complexes, characterized by a redox-active single-metal-atom with biomimetic ligands, such as pyrolyzed cobalt–nitrogen–carbon (Co–Nx/C), have attracted considerable attention. Therefore, we reported the ORR mechanism of pyrolyzed Vitamin B12 using operando X-ray absorption spectroscopy coupled with electrochemical impedance spectroscopy, which enables operando monitoring of the oxygen binding site on the metal center. Our results revealed the preferential adsorption of oxygen at the Co2+ center, with end-on coordination forming a Co2+-oxo species. Furthermore, the charge transfer mechanism between the catalyst and reactant enables further Co–O species formation. These experimental findings, corroborated with first-principle calculations, provide insight into metal active-site geometry and structural evolution during ORR, which could be used for developing material design strategies for high-performance electrocatalysts for fuel cell applications.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bayikadi, Khasim Saheb</style></author><author><style face="normal" font="default" size="100%">Wu, Chien Ting</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Fang-Cheng Chou</style></author><author><style face="normal" font="default" size="100%">Raman Sankar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synergistic optimization of thermoelectric performance of Sb doped GeTe with a strained domain and domain boundaries</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2020</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D0TA00628A</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">5332 - 5341</style></pages><isbn><style face="normal" font="default" size="100%">2050-7488</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;In addition to the Ge-vacancy control of GeTe, the antimony (Sb) substitution of GeTe for the improvement of thermoelectric performance is explored for Ge1−xSbxTe with x = 0.08–0.12. The concomitant carrier concentration (n) and the aliovalent Sb ion substitution led to an optimal doping level of x = 0.10 to show ZT ∼ 2.35 near ∼800 K, which is significantly higher than those single- and multi-element substitution studies of the GeTe system reported in the literature. In addition, Ge0.9Sb0.1Te demonstrates an impressively high power factor of ∼36 μW cm−1 K−2 and a low thermal conductivity of ∼1.1 W m−1 K−1 at 800 K. The enhanced ZT level for Ge0.9Sb0.1Te is explained through a systematic investigation of micro-structural change and strain analysis from room temperature to 800 K. A significant reduction of lattice thermal conductivity (κlat) is identified and explained by the Sb substitution-introduced strained and widened domain boundaries for the herringbone domain structure of Ge0.9Sb0.1Te. The Sb substitution created multiple forms of strain near the defect centre, the herringbone domain structure, and widened tensile/compressive domain boundaries to support phonon scattering that covers a wide frequency range of the phonon spectrum to reduce lattice thermal conductivity effectively.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">10</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sainbileg, Batjargal</style></author><author><style face="normal" font="default" size="100%">Lai, Ying-Ren</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Hayashi, Michitoshi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The dual-defective SnS2 monolayers: promising 2D photocatalysts for overall water splitting</style></title><secondary-title><style face="normal" font="default" size="100%">Physical Chemistry Chemical Physics</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2019</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C9CP04649F</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><volume><style face="normal" font="default" size="100%">21</style></volume><pages><style face="normal" font="default" size="100%">26292 - 26300</style></pages><isbn><style face="normal" font="default" size="100%">1463-9076</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Photocatalytic water splitting is a promising way to produce hydrogen fuel from solar energy. In this regard, the search for new photocatalytic materials that can efficiently split water into hydrogen is essential. Here, using first-principles simulations, we demonstrate that the dual-defective SnS2 (Ni-SnS2-VS), by both single-atom nickel doping and sulfur monovacancies, becomes a promising two-dimensional photocatalyst compared with SnS2. The Ni-SnS2-VS monolayer, in particular, exhibits a suitable band alignment that perfectly overcomes the redox potentials for overall water splitting. The dual-defective monolayer displays remarkable photocatalytic activity, a spatially separated carrier, a broadened optical absorption spectrum, and enhanced adsorption energy of H2O. Therefore, the dual-defective SnS2 monolayer can serve as an efficient photocatalyst for overall water splitting to produce hydrogen fuel. Furthermore, a novel dual-defect method can be an effective strategy to enhance the photocatalytic behavior of 2D materials; it may pave inroads in the development of solar-fuel generation.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">48</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chang, Hui-Ching</style></author><author><style face="normal" font="default" size="100%">You, Hao-Jen</style></author><author><style face="normal" font="default" size="100%">Raman Sankar</style></author><author><style face="normal" font="default" size="100%">Yang, Ying-Jay</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhanced thermoelectric performance of BiCuTeO by excess Bi additions</style></title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Electrical conductivity (C)</style></keyword><keyword><style  face="normal" font="default" size="100%">Hot pressing (A)</style></keyword><keyword><style  face="normal" font="default" size="100%">Secondary phases</style></keyword><keyword><style  face="normal" font="default" size="100%">Thermal applications (E)</style></keyword><keyword><style  face="normal" font="default" size="100%">Thermal properties (C)</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2019</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0272884219302901</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">45</style></volume><pages><style face="normal" font="default" size="100%">9254 - 9259</style></pages><isbn><style face="normal" font="default" size="100%">0272-8842</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Thermoelectric (TE) devices used to convert waste heat directly into electricity are highly desirable for alleviating the prevailing energy crisis and global climate-change issues. Among the various TE materials available, metal oxides exhibit high thermal and chemical stabilities in air, and are hence, preferred for use in many TE applications. However, most of them possess TE figures of merit (ZT) that are below the applicable value of 2, in the mid-temperature region (from 250 to 600 °C). In a previous work, the removal of a small amount of Bi from BiCuSeO was found to improve the ZT of BiCuSeO. In this work, we pursue another track and study the TE performance of BiCuTeO after the addition of up to 6% excess Bi. Bi1+xCuTeO (x = 0.00–0.06) samples were prepared by solid-state reactions, followed by hot-pressing to form pellets. By adding a stoichiometric excess of Bi into BiCuTeO, 16% enhancement in power factor was achieved at 450 °C. This enhancement can be attributed to the increase in the Seebeck coefficient because of the appearance of secondary phases. Detailed characterizations and discussions of the effect of the nominal excess Bi in BiCuTeO are presented in this paper. The findings of this study can be applied in the investigation of novel high-performance TE materials.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">7, Part A</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bayikadi, Khasim Saheb</style></author><author><style face="normal" font="default" size="100%">Raman Sankar</style></author><author><style face="normal" font="default" size="100%">Wu, Chien Ting</style></author><author><style face="normal" font="default" size="100%">Xia, Chengliang</style></author><author><style face="normal" font="default" size="100%">Chen, Yue</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Fang-Cheng Chou</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhanced thermoelectric performance of GeTe through in situ microdomain and Ge-vacancy control</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2019</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C9TA03503F</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">15181 - 15189</style></pages><isbn><style face="normal" font="default" size="100%">2050-7488</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;A highly reproducible sample preparation method for pure GeTe in a rhombohedral structure without converting to the cubic structure up to ∼500 °C is reported to show control of the Ge-vacancy level and the corresponding herringbone-structured microdomains. The thermoelectric figure-of-merit (ZT) for GeTe powder could be raised from ∼0.8 to 1.37 at high temperature (HT) near ∼500 °C by tuning the Ge-vacancy level through the applied reversible in situ route, which made it highly controllable and reproducible. The enhanced ZT of GeTe was found to be strongly correlated with both its significantly increased Seebeck coefficient (∼161 μV K−1 at 500 °C) and reduced thermal conductivity (∼2.62 W m−1 K−1 at 500 °C) for a sample with nearly vacancy-free thicker herringbone-structured microdomains in the suppressed rhombohedral-to-cubic structure phase transformation. The microdomain and crystal structures were identified with HR-TEM (high-resolution transmission electron microscopy) and powder X-ray diffraction (XRD), while electron probe micro-analysis (EPMA) was used to confirm the stoichiometry changes of Ge : Te. Theoretical calculations for GeTe with various Ge-vacancy levels suggested that the Fermi level shifts toward the valence band as a function of increasing the Ge-vacancy level, which is consistent with the increased hole-type carrier concentration (n) and effective mass (m*) deduced from the Hall measurements. The uniquely prepared sample of a near-vacancy-free GeTe in a rhombohedral structure at high temperature favoured an enhanced Seebeck coefficient in view of the converging L- and Σ-bands of the heavy effective mass at the Fermi level, while the high density domain boundaries for the domain of low carrier density were shown to reduce the total thermal conductivity effectively.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">25</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chang, Hui-Ching</style></author><author><style face="normal" font="default" size="100%">You, Hao-Jen</style></author><author><style face="normal" font="default" size="100%">Raman Sankar</style></author><author><style face="normal" font="default" size="100%">Yang, Ying-Jay</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhanced Thermoelectric Performance via Oxygen Manipulation in BiCuTeO</style></title><secondary-title><style face="normal" font="default" size="100%">MRS Advances</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">DEFECTS</style></keyword><keyword><style  face="normal" font="default" size="100%">oxide</style></keyword><keyword><style  face="normal" font="default" size="100%">scanning electron microscopy (SEM)</style></keyword><keyword><style  face="normal" font="default" size="100%">thermal conductivity</style></keyword><keyword><style  face="normal" font="default" size="100%">x-ray diffraction (XRD)</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2019</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.cambridge.org/core/article/enhanced-thermoelectric-performance-via-oxygen-manipulation-in-bicuteo/B2780167E3037CD80728B44E2FEBF5E7</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">Materials Research Society</style></publisher><volume><style face="normal" font="default" size="100%">4</style></volume><pages><style face="normal" font="default" size="100%">499-505</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;BiCuTeO is a potential thermoelectric material owing to its low thermal conductivity and high carrier concentration. However, the thermoelectric performance of BiCuTeO is still below average and has much scope for improvement. In this study, we manipulated the nominal oxygen content in BiCuTeO and synthesized BiCuTeOx (x = 0.94–1.06) bulks by a solid-state reaction and pelletized them by a cold-press method. The power factor was enhanced by varying the nominal oxygen deficiency due to the increased Seebeck coefficient. The thermal conductivity was also reduced due to the decrease in lattice thermal conductivity owing to the small grain size generated by the optimal nominal oxygen content. Consequently, the ZT value was enhanced by ∼11% at 523 K for stoichiometric BiCuTeO0.94 compared to BiCuTeO. Thus, optimal oxygen manipulation in BiCuTeO can enhance the thermoelectric performance. This study can be applied to developing oxides with high thermoelectric performances.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">8</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sabhapathy, Palani</style></author><author><style face="normal" font="default" size="100%">Liao, Chen-Cheng</style></author><author><style face="normal" font="default" size="100%">Wei-Fu Chen</style></author><author><style face="normal" font="default" size="100%">Tsu-chin Chou</style></author><author><style face="normal" font="default" size="100%">Indrajit Shown</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Yan-Gu Lin</style></author><author><style face="normal" font="default" size="100%">Jyh-Fu Lee</style></author><author><style face="normal" font="default" size="100%">Tsai, Ming-Kang</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Highly efficient nitrogen and carbon coordinated N–Co–C electrocatalysts on reduced graphene oxide derived from vitamin-B12 for the hydrogen evolution reaction</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2019</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C8TA10935D</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">7179 - 7185</style></pages><isbn><style face="normal" font="default" size="100%">2050-7488</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Exploring electrocatalysts composed of earth-abundant elements for a highly efficient hydrogen evolution reaction (HER) is scientifically and technologically important for electrocatalytic water splitting. In this work, we report HER properties of acid treated pyrolyzed vitamin B12 supported on reduced graphene oxide (B12/G800A) that shows an extraordinarily enhanced catalytic activity with low overpotential (115 mV vs. RHE at 10 mA cm−2), which is better than that of most traditional nonprecious metal catalysts in acidic media. Stability tests through long-term potential cycles and at a constant current density confirm the exceptional durability of the catalyst. Notably, the B12/G800A catalyst exhibits extremely high turnover frequencies per cobalt site in acid, for example, 0.85 and 11.46 s−1 at overpotentials of 100 and 200 mV, respectively, which are higher than those reported for other scalable non-precious metal HER catalysts. Moreover, it has been conjectured that the covalency of Co–C and Co–N bonds affects HER activities by comparing the extended X-ray absorption fine structure (EXAFS) spectra of the B12/G800A. High-temperature treatment can modify the Co-corrin structure of B12 to form Co–C bonds along with Co–N, which broadens the band of cobalt, essentially lowering the d-band center from its Fermi level. The lower d-band center leads to a moderate hydrogen binding energy, which is favorable for hydrogen adsorption and desorption.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">12</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Abhishek Pathak</style></author><author><style face="normal" font="default" size="100%">Shen, Jing-Wen</style></author><author><style face="normal" font="default" size="100%">Muhammad Usman</style></author><author><style face="normal" font="default" size="100%">Wei, Ling-Fang</style></author><author><style face="normal" font="default" size="100%">Shruti Mendiratta</style></author><author><style face="normal" font="default" size="100%">Chang, Yu-Shin</style></author><author><style face="normal" font="default" size="100%">Sainbileg, Batjargal</style></author><author><style face="normal" font="default" size="100%">Ngue, Chin-May</style></author><author><style face="normal" font="default" size="100%">Ruei-San Chen</style></author><author><style face="normal" font="default" size="100%">Hayashi, Michitoshi</style></author><author><style face="normal" font="default" size="100%">Tzuoo-Tsair Luo</style></author><author><style face="normal" font="default" size="100%">Fu-Rong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Tseng, Tien-Wen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuang-Lieh Lu</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Integration of a (–Cu–S–)n plane in a metal–organic framework affords high electrical conductivity</style></title></titles><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2019</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1038/s41467-019-09682-0</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">1721</style></pages><isbn><style face="normal" font="default" size="100%">2041-1723</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Designing highly conducting metal–organic frameworks (MOFs) is currently a subject of great interest for their potential applications in diverse areas encompassing energy storage and generation. Herein, a strategic design in which a metal–sulfur plane is integrated within a MOF to achieve high electrical conductivity, is successfully demonstrated. The MOF {[Cu2(6-Hmna)(6-mn)]·NH4}n (1, 6-Hmna = 6-mercaptonicotinic acid, 6-mn = 6-mercaptonicotinate), consisting of a two dimensional (–Cu–S–)n plane, is synthesized from the reaction of Cu(NO3)2, and 6,6′-dithiodinicotinic acid via the in situ cleavage of an S–S bond under hydrothermal conditions. A single crystal of the MOF is found to have a low activation energy (6 meV), small bandgap (1.34 eV) and a highest electrical conductivity (10.96 S cm−1) among MOFs for single crystal measurements. This approach provides an ideal roadmap for producing highly conductive MOFs with great potential for applications in batteries, thermoelectric, supercapacitors and related areas.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Fang-Yu Fu</style></author><author><style face="normal" font="default" size="100%">Indrajit Shown</style></author><author><style face="normal" font="default" size="100%">Li, Chia-Shuo</style></author><author><style face="normal" font="default" size="100%">Putikam Raghunath</style></author><author><style face="normal" font="default" size="100%">Lin, Tsai-Yu</style></author><author><style face="normal" font="default" size="100%">Tadesse Billo</style></author><author><style face="normal" font="default" size="100%">Heng-Liang Wu</style></author><author><style face="normal" font="default" size="100%">Chih-I Wu</style></author><author><style face="normal" font="default" size="100%">Chung, Po-Wen</style></author><author><style face="normal" font="default" size="100%">Lin, Ming-Chang</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">KSCN-induced Interfacial Dipole in Black TiO2 for Enhanced Photocatalytic CO2 Reduction</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; InterfacesACS Applied Materials &amp; Interfaces</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2019</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acsami.9b06264</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">25186 - 25194</style></pages><isbn><style face="normal" font="default" size="100%">1944-8244</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">n/a</style></abstract><issue><style face="normal" font="default" size="100%">28</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;doi: 10.1021/acsami.9b06264&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chen, Jyh-Chein</style></author><author><style face="normal" font="default" size="100%">Hsiao, You-Rong</style></author><author><style face="normal" font="default" size="100%">Liu, Yin-Cheng</style></author><author><style face="normal" font="default" size="100%">Ping-Yen Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Polybenzimidazoles containing heterocyclic benzo[c]cinnoline structure prepared by sol-gel process and acid doping level adjustment for high temperature PEMFC application</style></title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Benzo[]cinnoline</style></keyword><keyword><style  face="normal" font="default" size="100%">Fuel cell</style></keyword><keyword><style  face="normal" font="default" size="100%">Proton exchange membrane</style></keyword><keyword><style  face="normal" font="default" size="100%">Sol-gel process</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2019</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0032386119308201</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">182</style></volume><pages><style face="normal" font="default" size="100%">121814</style></pages><isbn><style face="normal" font="default" size="100%">0032-3861</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Polybenzimidazoles containing heterocyclic benzo[c]cinnoline structure are synthesized from 3,8-benzo[c]cinnoline dicarboxylic acid, terephthalic acid and 3,3′-diaminobenzidine. Their membranes are prepared by sol-gel process, involving the conversion of polymer solution in polyphosphoric acid to phosphoric acid. The acid doping levels of the as-prepared membranes increase as the contents of benzo[c]cinnoline increase, indicating good interaction between phosphoric acid and benzo[c]cinnoline structure. The as-prepared membranes with high acid doping levels might lead to the dissolution of membranes in phosphoric acid at temperature higher than 120 °C. A new method is proposed to adjust acid doping levels by immersing the as-prepared membranes in diluted phosphoric acid solutions of various concentrations. The adjusted membranes (acid doping levels around 30 PA RU−1) exhibit enhanced mechanical properties with tensile strength in the range of 4.1–5.2 MPa. The proton conductivity of adjusted membranes maintain at 0.15–0.17 S cm−1 at 160 °C under ambient atmosphere without humidification. The single cells based on the adjusted membranes exhibit open circuit voltages and peak power densities from 0.89 to 0.91 V and 691–1253 mW cm−2 at 160 °C, respectively. Compared to other polybenzimidazole membranes prepared by sol-gel process, the adjusted polybenzimidazoles show higher mechanical strength and better single cell performance.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Prem Kumar, D S</style></author><author><style face="normal" font="default" size="100%">Tippireddy, Sahil</style></author><author><style face="normal" font="default" size="100%">Anbalagan Ramakrishnan</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Malar, P</style></author><author><style face="normal" font="default" size="100%">Mallik, Ramesh Chandra</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Thermoelectric and electronic properties of chromium substituted tetrahedrite</style></title><secondary-title><style face="normal" font="default" size="100%">Semiconductor Science and Technology</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2019</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1088/1361-6641/aafa31</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">IOP Publishing</style></publisher><volume><style face="normal" font="default" size="100%">34</style></volume><pages><style face="normal" font="default" size="100%">035017</style></pages><isbn><style face="normal" font="default" size="100%">0268-12421361-6641</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Cr substituted tetrahedrites with the chemical formula Cu12−xCrxSb4S13 (x = 0.15, 0.25, 0.35, 0.5, 0.75, 1.0) have been synthesised for thermoelectric study. Cr substitutes at the Cu site to optimize the thermoelectric properties and achieve a higher figure of merit (zT). X-Ray diffraction (XRD) analysis revealed that the tetrahedrite is the major phase with minor impurity phases. Electron probe microanalysis (EPMA) shows the formation of tetrahedrite main phase with near stoichiometry and the presence of Cu3SbS4, CuSbS2 and Sb as secondary phases. X-ray photoelectron spectroscopy (XPS) shows the oxidation state of Cu, Sb and S as +1, +3 and −2, respectively, whereas for Cr, it could not be identified. Temperature-dependent magnetic susceptibility of sample x = 0.75 shows antiferromagnetic correlation originating from the Cr ion. The calculated effective magnetic moment of 2.83 μB per Cr atom indicates the presence of Cr+4 in this sample. The decrease in the electrical resistivity upon doping indicates the compensation of holes due to the substitution of Cr at the Cu site. But the x = 0.35 sample is not following the trend due to larger compensation of holes with an activation energy of 124.6 meV. The temperature-dependent behaviour of electrical resistivity shows the shift in the Fermi level from the valance band towards the band gap. The absolute Seebeck coefficient is positive throughout the temperature range and follows a similar trend as that of electrical resistivity, with the exception of the x = 0.35 sample. The electronic thermal conductivity reduces due to hole compensation caused by Cr substitution. Moreover, the substitution of Cr effectively reduces the lattice thermal conductivity due to point defect scattering of phonons. A maximum zT of 1.0 is achieved for sample x = 0.35 at 700 K.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Das, Sayan</style></author><author><style face="normal" font="default" size="100%">Valiyaveettil, Suneesh Meledath</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Suwas, Satyam</style></author><author><style face="normal" font="default" size="100%">Mallik, Ramesh Chandra</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Thermoelectric properties of Mn doped BiCuSeO</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Research Express</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2019</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1088/2053-1591/aaf710</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">IOP Publishing</style></publisher><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">086305</style></pages><isbn><style face="normal" font="default" size="100%">2053-1591</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;BiCuSeO is a promising thermoelectric material having earth-abundant non-toxic constituents and favourable thermoelectric properties like ultra-low thermal conductivity. In this study, Mn+2 has been introduced at the Bi+3 site to increase hole concentration as well as Seebeck coefficient, through aliovalent doping and magnetic impurity incorporation respectively. Samples were prepared through two-step solid state synthesis with the composition Bi1-xMnxCuSeO (x = 0.0, 0.04, 0.06, 0.08, 0.10 and 0.12). X-ray diffraction patterns confirmed the tetragonal (space group: P4/nmm) crystal structure of BiCuSeO as well as phase purity of the samples. The Seebeck coefficient and electrical resistivity had a decreasing trend with increasing doping fraction owing to the generation of charge carriers. The samples with x = 0.04 and 0.06 showed temperature independent Seebeck coefficient above 523 K, which is a signature of small polaron hopping. While the Seebeck coefficient of the samples with x = 0.08, 0.10 and 0.12 increased above 523 K due to the combination of localized and extended states. The thermal conductivity was dominated by the lattice part of the thermal conductivity. As a result of moderate Seebeck coefficient and low electrical resistivity, the highest power factor of 0.284 mW m−1-K2 was obtained for the Bi0.92Mn0.08CuSeO at 773 K, leading to a maximum zT of 0.4 at 773.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">8</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Roy, Pradip</style></author><author><style face="normal" font="default" size="100%">Kumar</style></author><author><style face="normal" font="default" size="100%">Haider, Golam</style></author><author><style face="normal" font="default" size="100%">Tsu-chin Chou</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Yang-Fang Chen</style></author><author><style face="normal" font="default" size="100%">Liang, Chi-Te</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ultrasensitive Gas Sensors Based on Vertical Graphene Nanowalls/SiC/Si Heterostructure</style></title><secondary-title><style face="normal" font="default" size="100%">ACS SensorsACS Sensors</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2019</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acssensors.8b01312</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">4</style></volume><pages><style face="normal" font="default" size="100%">406 - 412</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">n/a</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;doi: 10.1021/acssensors.8b01312&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Wei-ChaoChen</style></author><author><style face="normal" font="default" size="100%">Cheng-YingChen</style></author><author><style face="normal" font="default" size="100%">Yi-Rung Lin</style></author><author><style face="normal" font="default" size="100%">Jan-Kai Chang</style></author><author><style face="normal" font="default" size="100%">Chun-Hsiang Chen</style></author><author><style face="normal" font="default" size="100%">Ya-Ping Chiu</style></author><author><style face="normal" font="default" size="100%">Chih-I. Wu</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Interface engineering of CdS/CZTSSe heterojunctions for enhancing the Cu2ZnSn(S,Se)4 solar cell efficiency</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Today Energy</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">CdS</style></keyword><keyword><style  face="normal" font="default" size="100%">CZTSSe</style></keyword><keyword><style  face="normal" font="default" size="100%">Heterojunction</style></keyword><keyword><style  face="normal" font="default" size="100%">Soft-baking</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S2468606919300097</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">256 - 266</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Interface engineering of CdS/CZTS(Se) is an important aspect of improving the performance of buffer/absorber heterojunction combination. It has been demonstrated that the crossover phenomenon due to the interface recombination can be drastically eliminated by interface modification. Therefore, in-depth studies across the CdS/CZTS(Se) junction properties, as well as effective optimization processes, are very crucial for achieving high-efficiency CZTSSe solar cells. Here, we present a comprehensive study on the effects of soft-baking (SB) temperature on the junction properties and the corresponding optoelectronic and interface-structural properties. Based on in-depth photoemission studies corroborated with structural and composition analysis, we concluded that interdiffusion and intermixing of CZTSSe and CdS phases occurred on the Cu-poor surface of CZTSSe at elevated SB temperatures, and the interface dipole moments induced by electrostatic potential fluctuation were thus significantly eliminated. In contrast, with low SB temperature, the CdS/CZTSSe heterojunction revealed very sharp interface with very short interdiffusion, forming interface dipole moments and drastically deteriorating device performance. These post thermal treatments also significantly suppress defect energy level of interface measured by admittance spectroscopy from 294 to 109 meV due to CdS/CZTSSe interdiffusion. Meanwhile, the interdiffusion effects on the shift of valence band maximum, conduction band minimum and band offset across the heterojunction of thermally treated CdS/CZTSSe interface are spatially resolved at the atomic scale by measuring the local density of states with cross-sectional scanning tunneling microscopy and spectroscopy. A significant enhancement in the power conversion efficiency from 4.88% to 8.48% is achieved by a facile interface engineering process allowing a sufficient intermixing of CdS/Cd and CZTSSe/Se phases without detrimental recombination centers.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">C.C. Yang</style></author><author><style face="normal" font="default" size="100%">C. H. Cheng</style></author><author><style face="normal" font="default" size="100%">Chen, T. H.</style></author><author><style face="normal" font="default" size="100%">Lin, Y. H.</style></author><author><style face="normal" font="default" size="100%">Y. C. Chi</style></author><author><style face="normal" font="default" size="100%">W. H. Tseng</style></author><author><style face="normal" font="default" size="100%">P. H. Chang</style></author><author><style face="normal" font="default" size="100%">C.Y. Chen</style></author><author><style face="normal" font="default" size="100%">K. H. Chen</style></author><author><style face="normal" font="default" size="100%">L. C. Chen</style></author><author><style face="normal" font="default" size="100%">C.I. Wu</style></author><author><style face="normal" font="default" size="100%">G. R. Lin</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ge-Rich SiGe Mode-Locker for Erbium-Doped Fiber Lasers</style></title><secondary-title><style face="normal" font="default" size="100%">IEEE Journal of Selected Topics in Quantum Electronics</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">ABSORPTION</style></keyword><keyword><style  face="normal" font="default" size="100%">chemical exfoliation</style></keyword><keyword><style  face="normal" font="default" size="100%">composition ratio dependent saturable absorption</style></keyword><keyword><style  face="normal" font="default" size="100%">EDFL pulsation</style></keyword><keyword><style  face="normal" font="default" size="100%">erbium</style></keyword><keyword><style  face="normal" font="default" size="100%">erbium-doped fiber lasers</style></keyword><keyword><style  face="normal" font="default" size="100%">fibre lasers</style></keyword><keyword><style  face="normal" font="default" size="100%">FILMS</style></keyword><keyword><style  face="normal" font="default" size="100%">Ge-rich SiGe mode-locker</style></keyword><keyword><style  face="normal" font="default" size="100%">Ge-Si alloys</style></keyword><keyword><style  face="normal" font="default" size="100%">laser mode locking</style></keyword><keyword><style  face="normal" font="default" size="100%">laser tuning</style></keyword><keyword><style  face="normal" font="default" size="100%">nonstoichiometric saturable absorbers</style></keyword><keyword><style  face="normal" font="default" size="100%">Nonstoichiometric SiGe</style></keyword><keyword><style  face="normal" font="default" size="100%">optical fabrication</style></keyword><keyword><style  face="normal" font="default" size="100%">Optical fibers</style></keyword><keyword><style  face="normal" font="default" size="100%">optical pulse generation</style></keyword><keyword><style  face="normal" font="default" size="100%">optical saturable absorption</style></keyword><keyword><style  face="normal" font="default" size="100%">passive mode-locking</style></keyword><keyword><style  face="normal" font="default" size="100%">saturable absorption</style></keyword><keyword><style  face="normal" font="default" size="100%">self-amplitude modulation</style></keyword><keyword><style  face="normal" font="default" size="100%">self-phase modulation</style></keyword><keyword><style  face="normal" font="default" size="100%">SiGe</style></keyword><keyword><style  face="normal" font="default" size="100%">Silicon germanium</style></keyword><keyword><style  face="normal" font="default" size="100%">soliton compression</style></keyword><keyword><style  face="normal" font="default" size="100%">time 338 fs to 346 fs</style></keyword><keyword><style  face="normal" font="default" size="100%">time 730 fs</style></keyword><keyword><style  face="normal" font="default" size="100%">time 760 fs</style></keyword><keyword><style  face="normal" font="default" size="100%">time 820 fs</style></keyword><keyword><style  face="normal" font="default" size="100%">tunable nonlinear modulation depth</style></keyword><keyword><style  face="normal" font="default" size="100%">ultrafast fiber laser</style></keyword><keyword><style  face="normal" font="default" size="100%">ultrafast fiber lasers</style></keyword><keyword><style  face="normal" font="default" size="100%">Ultrafast optics</style></keyword><keyword><style  face="normal" font="default" size="100%">vaporized synthesis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May-June 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">24</style></volume><pages><style face="normal" font="default" size="100%">1 - 10</style></pages><isbn><style face="normal" font="default" size="100%">1077-260X</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Cheng-YingChen</style></author><author><style face="normal" font="default" size="100%">Bandiyah Sri Aprillia</style></author><author><style face="normal" font="default" size="100%">Wei-ChaoChen</style></author><author><style face="normal" font="default" size="100%">Yen-Ching Teng</style></author><author><style face="normal" font="default" size="100%">Chih-Yuan Chiu</style></author><author><style face="normal" font="default" size="100%">Ruei-San Chen</style></author><author><style face="normal" font="default" size="100%">Jih-Shang Hwang</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Above 10% efficiency earth-abundant Cu2ZnSn(S,Se)4 solar cells by introducing alkali metal fluoride nanolayers as electron-selective contacts</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Alkali metal fluoride</style></keyword><keyword><style  face="normal" font="default" size="100%">CZTSSe</style></keyword><keyword><style  face="normal" font="default" size="100%">Electron-selective contacts</style></keyword><keyword><style  face="normal" font="default" size="100%">Kesterite</style></keyword><keyword><style  face="normal" font="default" size="100%">Open-circuit voltage deficit</style></keyword><keyword><style  face="normal" font="default" size="100%">Solar cells</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S2211285518304233</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">51</style></volume><pages><style face="normal" font="default" size="100%">597 - 603</style></pages><isbn><style face="normal" font="default" size="100%">2211-2855</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The present investigation mainly addresses the open circuit voltage (Voc) issue in kesterite based Cu2ZnSn(S,Se)4 solar cells by simply introducing alkali metal fluoride nanolayers (~ several nm NaF, or LiF) to lower the work functions of the front ITO contacts without conventional hole-blocking ZnO layers. Kelvin probe measurements confirmed that the work function of the front ITO decreases from 4.82 to 3.39 and 3.65 eV for NaF and LiF, respectively, resulting in beneficial band alignment for electron collection and/or hole blocking on top electrodes. Moreover, a 10.4% power conversion efficiency (~ 11.5% in the cell effective area) CZTSSe cell with improved Voc of up to 90 mV has been attained. This demonstration may provide a new direction of further boosting the performance of copper chalcogenide based solar cells as well.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Indrajit Shown</style></author><author><style face="normal" font="default" size="100%">Satyanarayana Samireddi</style></author><author><style face="normal" font="default" size="100%">Chang, Yu-Chung</style></author><author><style face="normal" font="default" size="100%">Putikam, Raghunath</style></author><author><style face="normal" font="default" size="100%">Chang, Po-Han</style></author><author><style face="normal" font="default" size="100%">Sabbah, Amr</style></author><author><style face="normal" font="default" size="100%">Fang-Yu Fu</style></author><author><style face="normal" font="default" size="100%">Wei-Fu Chen</style></author><author><style face="normal" font="default" size="100%">Chih-I Wu</style></author><author><style face="normal" font="default" size="100%">Yu, Tsyr-Yan</style></author><author><style face="normal" font="default" size="100%">Chung, Po-Wen</style></author><author><style face="normal" font="default" size="100%">M. C. Lin</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Carbon-doped SnS2 nanostructure as a high-efficiency solar fuel catalyst under visible light</style></title><secondary-title><style face="normal" font="default" size="100%">Nature Communications</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1038/s41467-017-02547-4</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">169</style></pages><isbn><style face="normal" font="default" size="100%">2041-1723</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Photocatalytic formation of hydrocarbons using solar energy via artificial photosynthesis is a highly desirable renewable-energy source for replacing conventional fossil fuels. Using an l-cysteine-based hydrothermal process, here we synthesize a carbon-doped SnS2 (SnS2-C) metal dichalcogenide nanostructure, which exhibits a highly active and selective photocatalytic conversion of CO2 to hydrocarbons under visible-light. The interstitial carbon doping induced microstrain in the SnS2 lattice, resulting in different photophysical properties as compared with undoped SnS2. This SnS2-C photocatalyst significantly enhances the CO2 reduction activity under visible light, attaining a photochemical quantum efficiency of above 0.7%. The SnS2-C photocatalyst represents an important contribution towards high quantum efficiency artificial photosynthesis based on gas phase photocatalytic CO2 reduction under visible light, where the in situ carbon-doped SnS2 nanostructure improves the stability and the light harvesting and charge separation efficiency, and significantly enhances the photocatalytic activity.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">K.P.O., Mahesh</style></author><author><style face="normal" font="default" size="100%">Indrajit Shown</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Yian Tai</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Flexible sensor for dopamine detection fabricated by the direct growth of α-Fe2O3 nanoparticles on carbon cloth</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Surface Science</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">-FeO</style></keyword><keyword><style  face="normal" font="default" size="100%">Amperometry</style></keyword><keyword><style  face="normal" font="default" size="100%">Biosensor</style></keyword><keyword><style  face="normal" font="default" size="100%">Carbon cloth</style></keyword><keyword><style  face="normal" font="default" size="100%">Dopamine</style></keyword><keyword><style  face="normal" font="default" size="100%">Flexible</style></keyword><keyword><style  face="normal" font="default" size="100%">Wearable</style></keyword><keyword><style  face="normal" font="default" size="100%">α</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0169433217325266</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">427</style></volume><pages><style face="normal" font="default" size="100%">387 - 395</style></pages><isbn><style face="normal" font="default" size="100%">0169-4332</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;AbstractPorous α-Fe2O3 nanoparticles are directly grown on acid treated carbon cloth (ACC) using a simple hydrothermal method (denoted as ACC-α-Fe2O3) for employment as a flexible and wearable electrochemical electrode. The catalytic activity of ACC-α-Fe2O3 allowing the detection of dopamine (DA) is systematically investigated. The results showed that the ACC-α-Fe2O3 electrode exhibits impressive electrochemical sensitivity, stability and selectivity for the detection of DA. The detection limit determined with the amperometric method appears to be around 50nM with a linear range of 0.074–113μM. The impressive DA sensing ability of the as prepared ACC-α-Fe2O3 electrode is due to the good electrochemical behavior and high electroactive surface area (19.96cm2) of α-Fe2O3 nanoparticles anchored on the highly conductive ACC. It is worth noting that such remarkable sensing properties can be maintained even when the electrode is in a folded configuration.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;n/a&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rajeev Gandhi, J.</style></author><author><style face="normal" font="default" size="100%">Nehru, Raja</style></author><author><style face="normal" font="default" size="100%">Chen, Sheng-Ming</style></author><author><style face="normal" font="default" size="100%">Raman Sankar</style></author><author><style face="normal" font="default" size="100%">Bayikadi, Khasim Saheb</style></author><author><style face="normal" font="default" size="100%">Sureshkumar, Palanivel</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Influence of GeP precipitates on the thermoelectric properties of P-type GeTe and Ge0.9−xPxSb0.1Te compounds</style></title><secondary-title><style face="normal" font="default" size="100%">CrystEngComm</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C8CE01134F</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><volume><style face="normal" font="default" size="100%">20</style></volume><pages><style face="normal" font="default" size="100%">6449 - 6457</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Germanium telluride (GeTe) is a very well known IV–VI group semiconducting material with the advantageous property of showing metallic conduction, which materializes from its superior carrier concentration (n) (high number of Ge vacancies). A systematic investigation into the thermoelectric properties (TEP) of GeTe was reported by way of carrier concentration (n) engineering. The present investigation focuses on studying the effects of doping (antimony – Sb) and co-doping (phosphorus – P) on the TEP of GeTe. In order to understand the system, we have prepared p-type GeTe and Ge0.9−xPxSb0.1Te (x = 0, 0.01, 0.03, or 0.05) samples via a non-equilibrium solid state melt quenching (MQ) process, followed by hot press consolidation. Temperature dependent synchrotron X-ray diffraction studies reveal a phase transition from rhombohedral to simple cubic in the Ge0.9−xPxSb0.1Te system at 573 K, which is clearly reflected in the TEP. Further high resolution transmission electron microscopy (HRTEM) studies reveal the pseudo-cubic nature of the sample. However, powder X-ray diffraction (PXRD) and field emission scanning electron microscopy (FESEM) images and energy dispersive X-ray spectroscopy (EDX) studies confirm the presence of germanium phosphide (GeP) in all P-doped samples. The presence of a secondary phase and point defects (Sb &amp;amp; P) enhanced the additional scattering effects in the system, which influenced the Seebeck coefficient and thermal conductivity of GeTe. A significant enhancement in the Seebeck coefficient (S) to ∼225 μV K−1 and a drastic reduction in thermal conductivity (κ) to ∼1.2 W mK−1 effectively enhanced the figure-of-merit (ZT) to ∼1.72 at 773 K for Ge0.87P0.03Sb0.1Te, which is a ∼3 fold increase for GeTe. Finally, P co-doped Ge0.9Sb0.1Te demonstrates an enhancement in ZT, making it a good candidate material for power generation applications.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">41</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Roy, Pradip Kumar</style></author><author><style face="normal" font="default" size="100%">Haider, Golam</style></author><author><style face="normal" font="default" size="100%">Lin, Hung-I</style></author><author><style face="normal" font="default" size="100%">Liao, Yu-Ming</style></author><author><style face="normal" font="default" size="100%">Lu, Cheng-Hsin</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Shih, Wei-Heng</style></author><author><style face="normal" font="default" size="100%">Liang, Chi-Te</style></author><author><style face="normal" font="default" size="100%">Yang-Fang Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Multicolor Ultralow-Threshold Random Laser Assisted by Vertical-Graphene Network</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Optical MaterialsAdvanced Optical Materials</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">perovskite nanocrystals</style></keyword><keyword><style  face="normal" font="default" size="100%">plasmonic</style></keyword><keyword><style  face="normal" font="default" size="100%">random lasers</style></keyword><keyword><style  face="normal" font="default" size="100%">ultralow threshold</style></keyword><keyword><style  face="normal" font="default" size="100%">vertical graphene nanowalls</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/adom.201800382</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">1800382</style></pages><isbn><style face="normal" font="default" size="100%">2195-1071</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Abstract Application of lasers is omnipresent in modern-day technology. However, preparation of a lasing device usually requires sophisticated design of the materials and is costly, which may limit the suitable choice of materials and the lasing wavelengths. Random lasers, on the other hand, can circumvent the aforementioned shortcomings with simpler fabrication process, lower processing cost, material flexibility for any lasing wavelengths with lower lasing threshold, providing a roadmap for the design of super-bright lighting, displays, Li-Fi, etc. In this work, ultralow-threshold random laser action from semiconductor nanoparticles assisted by a highly porous vertical-graphene-nanowalls (GNWs) network is demonstrated. The GNWs embedded by the nanomaterials produce a suitable cavity for trapping the optical photons with semiconductor nanomaterials acting as the gain medium. The observed laser action shows ultralow values of threshold energy density ≈10 nJ cm?2 due to the strong photon trapping within the GNWs. The threshold pump fluence can be further lowered to ≈1 nJ cm?2 by coating Ag/SiO2 upon the GNWs due to the combined effect of photon trapping and strong plasmonic enhancement. In view of the growing demand of functional materials and novel technologies, this work provides an important step toward realization of high-performance optoelectronic devices.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">16</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;doi: 10.1002/adom.201800382&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Cheng-YingChen</style></author><author><style face="normal" font="default" size="100%">Bandiyah Sri Aprillia</style></author><author><style face="normal" font="default" size="100%">Wei-ChaoChen</style></author><author><style face="normal" font="default" size="100%">Yen-Ching Teng</style></author><author><style face="normal" font="default" size="100%">Chih-Yuan Chiu</style></author><author><style face="normal" font="default" size="100%">Ruei-San Chen</style></author><author><style face="normal" font="default" size="100%">Jih-Shang Hwang</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Above 10% Efficiency Earth-abundant Cu2ZnSn(S,Se)4 Solar Cells by Introducing Alkali Metal Fluoride Nanolayers as Electron-selective Contacts</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Solar cells</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S2211285518304233</style></url></web-urls></urls><pages><style face="normal" font="default" size="100%">-</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Abstract The present investigation mainly addresses the open circuit voltage (Voc) issue in kesterites based Cu2ZnSn(S,Se)4 solar cells by simply introducing alkali metal fluoride nanolayers (  several nm NaF, or LiF) to lower the work functions of the front İTO\} contacts without conventional hole-blocking ZnO layers. Kelvin probe measurements confirmed that the work function of the front İTO\} decreases from 4.82 to 3.39 and 3.65 eV for NaF and LiF, respectively, resulting in beneficial band alignment for electron collection and/or hole blocking on top electrodes. Moreover, a 10.4% power conversion efficiency ( 11.5% in the cell effective area) \{CZTSSe\} cell with improved Voc of up to 90 mV has been attained. This demonstration may provide a new direction of further boosting the performance of copper chalcogenide based solar cells as well.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jyh-Chien Chen</style></author><author><style face="normal" font="default" size="100%">Ping-Yen Chen</style></author><author><style face="normal" font="default" size="100%">Han-Yu Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Analysis and characterization of an atropisomeric ionomer containing quaternary ammonium groups</style></title><secondary-title><style face="normal" font="default" size="100%">Polymer</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anion exchange membrane</style></keyword><keyword><style  face="normal" font="default" size="100%">Atropisomerism</style></keyword><keyword><style  face="normal" font="default" size="100%">Chiral axis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0032386118302015</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">141</style></volume><pages><style face="normal" font="default" size="100%">143 - 153</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Polyethersulfone ionomers containing quaternary ammoniums were prepared for the applications on alkaline anion exchange membrane (AAEM) fuel cells. The ionomers were synthesized from 2,2′-dimethyl-4,4′-biphenyldiol and bis(4-chlorophenyl) sulfone via nucleophilic substitution followed by bromination, quaternization and anion exchange reaction. The biphenyl structure in polymer main chain exhibited atropisomerism after bromination, leading to the anisochronous signals of geminal protons on bromomethyl groups in 1H NMR spectra. Model compounds were synthesized to confirm the atropisomerism by EI mass and 1H NMR spectra. The resonance peaks from five possible repeating units of brominated polyethersulfones in the 1H NMR spectra were identified and discussed in detail. The rotational barriers of biphenyl structures containing brominated methyl groups at 2 and 2′ positions were calculated by density functional theory. The properties of these polyethersulfone anion exchange membranes (AEMs) were characterized. Their IECs ranged from 0.81 to 1.75 mequiv/g. The corresponding water uptakes and dimensional changes were in the ranges of 19–42% and 12–38%, respectively. The tensile strength of an AEM (1.75MQAPES-OH) with an IEC of 1.75 mequiv/g remained 17 MPa even though the water uptake was 42%. The hydroxide conductivity of 1.75MQAPES-OH could reach 51.4 mS/cm at 98%RH and 80 °C. After alkaline stability test for 168 h, the AEMs degraded slightly in terms of their IECs and hydroxide conductivity.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tadesse Billo</style></author><author><style face="normal" font="default" size="100%">Fang-Yu Fu</style></author><author><style face="normal" font="default" size="100%">Putikam Raghunath</style></author><author><style face="normal" font="default" size="100%">Indrajit Shown</style></author><author><style face="normal" font="default" size="100%">Wei-Fu Chen</style></author><author><style face="normal" font="default" size="100%">Hsiang-Ting Lien</style></author><author><style face="normal" font="default" size="100%">Tzu-Hsien Shen</style></author><author><style face="normal" font="default" size="100%">Jyh-Fu Lee</style></author><author><style face="normal" font="default" size="100%">Ting-Shan Chan</style></author><author><style face="normal" font="default" size="100%">Kuo-You Huang</style></author><author><style face="normal" font="default" size="100%">Chih-I Wu</style></author><author><style face="normal" font="default" size="100%">M. C. Lin</style></author><author><style face="normal" font="default" size="100%">Jih-Shang Hwang</style></author><author><style face="normal" font="default" size="100%">Chih-Hao Lee</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ni-Nanocluster Modified Black TiO2 with Dual Active Sites for Selective Photocatalytic CO2 Reduction</style></title><secondary-title><style face="normal" font="default" size="100%">Small</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">artificial photosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">black TiO2</style></keyword><keyword><style  face="normal" font="default" size="100%">photocatalytic CO2 reduction</style></keyword><keyword><style  face="normal" font="default" size="100%">solar fuels</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/smll.201702928</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">2</style></number><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">1702928–n/a</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;One of the key challenges in artificial photosynthesis is to design a photocatalyst that can bind and activate the CO2 molecule with the smallest possible activation energy and produce selective hydrocarbon products. In this contribution, a combined experimental and computational study on Ni-nanocluster loaded black TiO2 (Ni/TiO2[Vo]) with built-in dual active sites for selective photocatalytic CO2 conversion is reported. The findings reveal that the synergistic effects of deliberately induced Ni nanoclusters and oxygen vacancies provide (1) energetically stable CO2 binding sites with the lowest activation energy (0.08 eV), (2) highly reactive sites, (3) a fast electron transfer pathway, and (4) enhanced light harvesting by lowering the bandgap. The Ni/TiO2[Vo] photocatalyst has demonstrated highly selective and enhanced photocatalytic activity of more than 18 times higher solar fuel production than the commercial TiO2 (P-25). An insight into the mechanisms of interfacial charge transfer and product formation is explored.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;1702928&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jian-Ming Chiu</style></author><author><style face="normal" font="default" size="100%">Tsu-chin Chou</style></author><author><style face="normal" font="default" size="100%">Deniz P. Wong</style></author><author><style face="normal" font="default" size="100%">Yi-Rung Lin</style></author><author><style face="normal" font="default" size="100%">Chin-An Shen</style></author><author><style face="normal" font="default" size="100%">Sunny Hy</style></author><author><style face="normal" font="default" size="100%">Bing-Joe Hwang</style></author><author><style face="normal" font="default" size="100%">Yian Tai</style></author><author><style face="normal" font="default" size="100%">Heng-Liang Wu</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A synergistic “cascade” effect in copper zinc tin sulfide nanowalls for highly stable and efficient lithium ion storage</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anode</style></keyword><keyword><style  face="normal" font="default" size="100%">Cascade effect</style></keyword><keyword><style  face="normal" font="default" size="100%">Copper zinc tin sulfide</style></keyword><keyword><style  face="normal" font="default" size="100%">High rate capability</style></keyword><keyword><style  face="normal" font="default" size="100%">Lithium ion batteries</style></keyword><keyword><style  face="normal" font="default" size="100%">Nanostructure</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S2211285517307954</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">44</style></volume><pages><style face="normal" font="default" size="100%">438 - 446</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">n/a</style></abstract><notes><style face="normal" font="default" size="100%">n/a</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Fang, Si-Ling</style></author><author><style face="normal" font="default" size="100%">Tsu-chin Chou</style></author><author><style face="normal" font="default" size="100%">Satyanarayana Samireddi</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Wei-Fu Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhanced hydrogen evolution reaction on hybrids of cobalt phosphide and molybdenum phosphide</style></title><secondary-title><style face="normal" font="default" size="100%">Royal Society open science</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2017/03/01</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.ncbi.nlm.nih.gov/pubmed/28405392</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">The Royal Society Publishing</style></publisher><volume><style face="normal" font="default" size="100%">4</style></volume><pages><style face="normal" font="default" size="100%">161016161016 - 161016</style></pages><isbn><style face="normal" font="default" size="100%">2054-57032054-5703</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Production of hydrogen from water electrolysis has stimulated the search of sustainable electrocatalysts as possible alternatives. Recently, cobalt phosphide (CoP) and molybdenum phosphide (MoP) received great attention owing to their superior catalytic activity and stability towards the hydrogen evolution reaction (HER) which rivals platinum catalysts. In this study, we synthesize and study a series of catalysts based on hybrids of CoP and MoP with different Co/Mo ratio. The HER activity shows a volcano shape and reaches a maximum for Co/Mo = 1. Tafel analysis indicates a change in the dominating step of Volmer-Hyrovský mechanism. Interestingly, X-ray diffraction patterns confirmed a major ternary interstitial hexagonal CoMoP(2) crystal phase is formed which enhances the electrochemical activity.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><notes><style face="normal" font="default" size="100%">n/a</style></notes><custom1><style face="normal" font="default" size="100%">28405392[pmid]</style></custom1><custom2><style face="normal" font="default" size="100%">PMC5383849[pmcid]</style></custom2><custom4><style face="normal" font="default" size="100%">rsos161016[PII]</style></custom4></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ebrahimi, Mahdi</style></author><author><style face="normal" font="default" size="100%">Samadi, Morasae</style></author><author><style face="normal" font="default" size="100%">Yousefzadeh, Samira</style></author><author><style face="normal" font="default" size="100%">Soltani, Mojtaba</style></author><author><style face="normal" font="default" size="100%">Rahimi, Alireza</style></author><author><style face="normal" font="default" size="100%">Tsu-chin Chou</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Moshfegh, Alireza Zaker</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Improved Solar-Driven Photocatalytic Activity of Hybrid Graphene Quantum Dots/ZnO Nanowires: A Direct Z-Scheme Mechanism</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Sustainable Chemistry &amp; EngineeringACS Sustainable Chemistry &amp; Engineering</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acssuschemeng.6b01738</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">5</style></volume><pages><style face="normal" font="default" size="100%">367 - 375</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">n/a</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;doi: 10.1021/acssuschemeng.6b01738&lt;/p&gt;
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shih-Wei Lee</style></author><author><style face="normal" font="default" size="100%">Jyh-Chien Chen</style></author><author><style face="normal" font="default" size="100%">Jin-An Wu</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis and Properties of Poly(ether sulfone)s with Clustered Sulfonic Groups for PEMFC Applications under Various Relative Humidity</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; InterfacesACS Applied Materials &amp; Interfaces</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acsami.7b00919</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">9805 - 9814</style></pages><isbn><style face="normal" font="default" size="100%">1944-8244</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">n/a</style></abstract><issue><style face="normal" font="default" size="100%">11</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;doi: 10.1021/acsami.7b00919&lt;/p&gt;
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size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhancement in Thermoelectric Properties of TiS2 by Sn Addition</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Electronic Materials</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2017</style></year></dates><pages><style face="normal" font="default" size="100%">1–8</style></pages></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jian-Ming Chiu</style></author><author><style face="normal" font="default" size="100%">E-Ming Chen</style></author><author><style face="normal" font="default" size="100%">Chuan-Pei Lee</style></author><author><style face="normal" font="default" size="100%">Indrajit Shown</style></author><author><style face="normal" font="default" size="100%">Venkatesh Tunuguntla</style></author><author><style face="normal" font="default" size="100%">Jui-Sheng Chou</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Yian Tai</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Geogrid-Inspired Nanostructure to Reinforce a CuxZnySnzS Nanowall Electrode for High-Stability Electrochemical Energy Conversion Devices</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Energy Materials</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2017</style></year></dates><volume><style face="normal" 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size="100%">Jenq-Wei Chen</style></author><author><style face="normal" font="default" size="100%">Fu-Rong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuang-Lieh Lu</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">High-κ Samarium-Based Metal–Organic Framework for Gate Dielectric Applications</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Appl. Mater. Interfaces</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2017</style></year></dates><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">21872–21878</style></pages><issue><style face="normal" font="default" size="100%">26</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Satyanarayana Samireddi</style></author><author><style face="normal" font="default" size="100%">Indrajit Shown</style></author><author><style face="normal" font="default" size="100%">Tzu-Hsien Shen</style></author><author><style face="normal" font="default" size="100%">Hsin-Chih Huang</style></author><author><style face="normal" font="default" size="100%">Ken-Tsung Wong</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hybrid bimetallic-N4 electrocatalyst derived from a pyrolyzed ferrocene–Co-corrole complex for oxygen reduction reaction</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2017</style></year></dates><urls><related-urls><url><style face="normal" font="default" size="100%">https://labs.iams.sinica.edu.tw/project/sites/default/files/chenkh/files/satya.pdf</style></url></related-urls></urls><volume><style face="normal" font="default" size="100%">5</style></volume><pages><style face="normal" font="default" size="100%">9279-9286</style></pages></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mohammad Qorbani</style></author><author><style face="normal" font="default" size="100%">Tsu-chin Chou</style></author><author><style face="normal" font="default" size="100%">Yi-Hsin Lee</style></author><author><style face="normal" font="default" size="100%">Satyanarayana Samireddi</style></author><author><style face="normal" font="default" size="100%">Naimeh Naseri</style></author><author><style face="normal" font="default" size="100%">Abhijit Ganguly</style></author><author><style face="normal" font="default" size="100%">Ali Esfandiar</style></author><author><style face="normal" font="default" size="100%">Chen-Hao Wang</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Alireza Z. 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Mater. Interfaces</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2017</style></year></dates><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">9805–9814</style></pages><issue><style face="normal" font="default" size="100%">11</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chuan-Pei Lee</style></author><author><style face="normal" font="default" size="100%">Wei-Fu Chen</style></author><author><style face="normal" font="default" size="100%">Tadesse Billo</style></author><author><style face="normal" font="default" size="100%">Yan-Gu Lin</style></author><author><style face="normal" font="default" size="100%">Fang-Yu Fu</style></author><author><style face="normal" font="default" size="100%">Satyanarayana Samireddi</style></author><author><style face="normal" font="default" size="100%">Chih-Hao Lee</style></author><author><style face="normal" font="default" size="100%">Jih-Shang Hwang</style></author><author><style face="normal" font="default" size="100%">Kuei-Hsien Chen</style></author><author><style face="normal" font="default" size="100%">Li-Chyong Chen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Beaded stream-like CoSe2 nanoneedle array for efficient hydrogen evolution electrocatalysis</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2016</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C6TA00464D</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><volume><style face="normal" font="default" size="100%">4</style></volume><pages><style face="normal" font="default" size="100%">4553 - 4561</style></pages><isbn><style face="normal" font="default" size="100%">2050-7488</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The development of earth-abundant and efficient electrocatalysts for the hydrogen evolution reaction (HER) is one of the keys to success for future green energy systems using hydrogen fuel. Nanostructuring of electrocatalysts is a promising way to enhance their electrocatalytic performance in the HER. In this study, pure pyrite-type beaded stream-like cobalt diselenide (CoSe2) nanoneedles are directly formed on flexible titanium foils through treating a cobalt oxide (Co3O4) nanoneedle array template with selenium vapor. The beaded stream-like CoSe2 nanoneedle electrode can drive the HER at a current density of 20 mA cm−2 with a small overpotential of 125 mV. Moreover, the beaded stream-like CoSe2 nanoneedle electrode remains stable in an acidic electrolyte for 3000 cycles and continuously splits water over a period of 18 hours. The enhanced electrochemical activity is facilitated by the unique three-dimensional hierarchical structure, the highly accessible surface active sites, the improved charge transfer kinetics and the highly attractive force between water and the surface of the nanoneedles that exceeds the surface tension of water.&lt;/p&gt;
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Flexible supercapacitors are governed by the fundamentals standard for the conventional capacitors but provide high flexibility, high charge storage and low resistance of electro active materials to achieve high capacitance performance. Conducting polymers (CPs) are among the most potential pseudocapacitor materials for the foundation of flexible supercapacitors, motivating the existing energy storage devices toward the future advanced flexible electronic applications due to their high redox active-specific capacitance and inherent elastic polymeric nature. This review focuses on different types of CPs-based supercapacitor, the relevant fabrication methods and designing concepts. It describes recent developments and remaining challenges in this field, and its impact on the future direction of flexible supercapacitor materials and relevant device fabrications.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><notes><style face="normal" font="default" size="100%">&lt;p&gt;doi: 10.1002/ese3.50&lt;/p&gt;
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