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Atomic structure and electronic properties of the two-dimensional (Au, Al)/Si(111)2 x 2 compound, {DEC 7}. PHYSICAL REVIEW B. 92:245407., Number {24}
Abstract
Ting, T-C, Hsu L-Y, Huang M-J, Horng E-C, Lu H-C, Hsu C-H, Jiang C-H, Jin B-Y, Peng S-M, Chen C-hsien.
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Energy-Level Alignment for Single-Molecule Conductance of Extended Metal-Atom Chains, DEC 21. Angew. Chem. Int. Ed.. 54:15734-15738., Number 52
Abstractn/a
Shown, I, Ganguly A, Chen L-C, Chen K-H.
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Conducting polymer-based flexible supercapacitor, 2015. Energy Science & EngineeringEnergy Science & Engineering. 3(1):2-26.: John Wiley & Sons, Ltd
AbstractAbstract Flexible supercapacitors, a state-of-the-art material, have emerged with the potential to enable major advances in for cutting-edge electronic applications. 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.
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Direct evidence of mitochondrial G-quadruplex DNA by using fluorescent anti-cancer agents. Nucleic Acids Res.. 43(21):10102-13.
Chen, K-I, Pan C-Y, Li K-H, Huang Y-C, Lu C-W, Tang C-Y, Su Y-W, Tseng L-W, Tseng K-C, Lin C-Y, Chen C-D, Lin S-S, Chen Y-T.
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Isolation and Identification of Post-Transcriptional Gene Silencing-Related Micro- RNAs by Functionalized Silicon Nanowire Field-effect Transistor. Scientific Reports. 5(17375):DOI:10.1038/srep17375.
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Characterization of molecular channel in photodissociation of SOCl2 at 248 nm: Cl2 probing by cavity ring-down absorption spectroscopy. Physical Chemistry Chemical Physics. 17:7838-7847., Number 12
AbstractA primary elimination channel of the chlorine molecule in the one-photon dissociation of SOCl2 at 248 nm was investigated using cavity ring-down absorption spectroscopy (CRDS). By means of spectral simulation, the ratio of the vibrational population in the v = 0, 1, and 2 levels was evaluated to be 1:(0.10 ± 0.02):(0.009 ± 0.005), corresponding to a Boltzmann vibrational temperature of 340 ± 30 K. The Cl2 molecular channel was obtained with a quantum yield of 0.4 ± 0.2 from the X1A′ ground state of SOCl2via internal conversion. The dissociation mechanism differs from a prior study where a smaller yield of <3% was obtained, initiated from the 21A′ excited state. Temperature-dependence measurements of the Cl2 fragment turn out to support our mechanism. With the aid of ab initio potential energy calculations, two dissociation routes to the molecular products were found, including one synchronous dissociation pathway via a three-center transition state (TS) and the other sequential dissociation pathway via a roaming-mediated isomerization TS. The latter mechanism with a lower energy barrier dominates the dissociation reaction. This journal is © the Owner Societies.
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