Oxygen reduction reaction on a polypyrrole-modified, carbon-supported cobalt hydroxide catalyst

被引:17
|
作者
Qin, Hai Ying [1 ]
Zhu, Kun Ning [1 ]
Ye, Li Qiang [1 ]
Li, Zhou Peng [1 ]
机构
[1] Zhejiang Univ, Dept Chem & Biol Engn, Hangzhou 310027, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Oxygen reduction reaction; Polypyrrole-modified carbon-supported cobalt hydroxide; Electrocatalytic activity; Catalytic site; Cell performance; BOROHYDRIDE FUEL-CELL; ALKALINE MEDIA; ELECTROCATALYSTS; PARTICLES; OXIDATION; CATHODE; ANODES; SITE; NI;
D O I
10.1016/j.jpowsour.2012.02.040
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
A series of polypyrrole (PPY)-modified carbon-supported Co(OH)(2) catalysts [Co(OH)(2)-PPY-C] with different types of carbon supports and the PPY and Co(OH)(2) contents are synthesized to investigate the effect of the Co-Nx and -C=N-C= sites on the oxygen reduction reaction (ORR). X-ray photoemission spectroscopy results reveal that the Co-Nx and -C=N-C= sites dominate the four- and two-electron transfer ORR, respectively. The carbon support and the PPY and Co(OH)(2) contents of the catalysts determine the distribution of the Co-Nx and -C=N-C= sites. The competition between these two sites determines the overall electron number of the ORR. A direct borohydride fuel cell using an optimal Co(OH)(2)-PPY-C as the cathode catalyst exhibits a maximum power density of 550 mW cm(-2) at 80 degrees C. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:203 / 209
页数:7
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