Browsing by Author "Chang, Tin-Yu"

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Electrochemical reduction of CO(2) by Cu(2)O-catalyzed carbon clothes
(2009-05-15)
Chang, Tin-Yu
;
Liang, Ru-Meng
;
Wu, Pu-Wei
;
Chen, Jing-Yu
;
Hsieh, Yu-Chi
Cu(2)O cubes with average edge lengths of 640 nm were prepared by a chemical reduction approach. The as-synthesized Cu(2)O particles were deposited on carbon clothes for electrochemical characterizations in cyclic voltammetry (CV) and potentiostatic measurements. In 0.5 M NaOH electrolytes saturated with N(2) or CO(2), both the Cu(2)O and carbon clothes were stable at the potential range of 0 to -1.7 V. Comparisons in the Current responses from the CV and potentiostatic measurements suggested the Cu(2)O with notable catalytic abilities for the CO(2) reduction. The mass activity was estimated at 0.94 mA/mg. Chemical analysis from gas chromatography confirmed the methanol to be the predominant product. (C) 2009 Elsevier B.V. All rights reserved.
Electrochemical reduction of CO2 by Cu2O-catalyzed carbon clothes
(2009-05-15)
Chang, Tin-Yu
;
Liang, Ru-Meng
;
Wu, Pu-Wei
;
Chen, Jing-Yu
;
Hsieh, Yu-Chi
Cu2O cubes with average edge lengths of 640 nm were prepared by a chemical reduction approach. The as-synthesized Cu2O particles were deposited on carbon clothes for electrochemical characterizations in cyclic voltammetry (CV) and potentiostatic measurements. In 0.5 M NaOH electrolytes saturated with N-2 or CO2, both the Cu2O and carbon clothes were stable at the potential range of 0 to -1.7 V. Comparisons in the Current responses from the CV and potentiostatic measurements suggested the Cu2O with notable catalytic abilities for the CO2 reduction. The mass activity was estimated at 0.94 mA/mg. Chemical analysis from gas chromatography confirmed the methanol to be the predominant product. (C) 2009 Elsevier B.V. All rights reserved.
Enhancement of bifunctional catalysis by Ir doping of La0.6Ca0.4CoO3 perovskites
(2008-10-15)
Chang, Yun-Min
;
Hsieh, Yu-Chi
;
Wu, Pu-Wei
;
Lai, Chun-Han
;
Chang, Tin-Yu
La0.6Ca0.4Co0.8Ir0.2O3 was prepared by solid state reaction synthesis from mixtures of La(NO3)(3)center dot 6H(2)O, Ca (NO3)(2)center dot 4H(2)O, Co(NO3)(3)center dot 6H(2)O, and IrO2 at stoichiometric ratio. Images from scanning electron microscopy on the as-synthesized powders exhibited particles in irregular shape at 100-250 nm in size. X-ray diffraction analysis confirmed the formation of perovskite without the rutile signals from IrO2, suggesting successful incorporation of Ir4+ at the Co cation sites. The carbon nanocapsules (CNCs) were used as an electrocatalyst support. Electrodes for electrochemical measurements were fabricated by depositing mixtures of CNCs, La0.6Ca0.4Co0.8Ir0.2O3 and polymeric binders on commercially available noncatalyzed gas diffusion electrodes. In alkaline electrolyte, the La0.6Ca0.4Co0.8Ir0.2O3/CNCs demonstrated superior performances than those of La0.6Ca0.4Co0.8Ir0.2O3/CNCs and IrO2/CNCs in both charging and discharging current-potential polarization measurements. (c) 2008 Elsevier B.V. All rights reserved.