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Electroactivity of tin modified platinum electrodes for ethanol electrooxidation
被引:149
作者:
Simoes, F. C.
dos Anjos, D. M.
Vigier, F.
Leger, J.-M.
Hahn, F.
Coutanceau, C.
Gonzalez, E. R.
Tremiliosi-Filho, G.
de Andrade, A. R.
Olivi, P.
Kokoh, K. B.
机构:
[1] Univ Poitiers, CNRS, UMR 6503, Equipe Electrocatalyse, F-86022 Poitiers, France
[2] Univ Sao Paulo, Dept Quim, Fac Filosofia Ciencias & Letras Ribeirao Preto, BR-14040901 Ribeirao Preto, Brazil
[3] Univ Sao Paulo, Inst Quim Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil
基金:
巴西圣保罗研究基金会;
关键词:
ethanol oxidation;
DEFC;
platinum-tin electrocatalyst;
D O I:
10.1016/j.jpowsour.2006.12.113
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Different electrochemical techniques like cyclic voltammetry and chronoamperometry and tests in a single direct ethanol fuel cell (DEFC) were used to evaluate the catalytic activity of various compositions of PtSn electrodes prepared by thermal decomposition for ethanol electrooxidation. This oxidation process was also investigated by in situ infrared reflectance spectroscopy to determine the presence of adsorbed intermediates. The experimental results showed that PtSn can oxidize ethanol mainly to acetaldehyde and acetic acid. Adsorbed CO was also found, which demonstrates that the rupture of the C-C bond in the ethanol molecule can also take place during the oxidation process. This intermediate species was oxidized to CO2 which was detected by IR spectroscopy and chromatography. With Pt90Sn10/C as anode catalyst, single DEFC tests carried out using MEAs with a geometric electrode area of 5 cm(2) allowed to produce a power density of ca. 72 mW cm(-2) at 110 degrees C. (C) 2007 Elsevier B.V. All rights reserved.
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页码:1 / 10
页数:10
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