TY - JOUR
T1 - Analysis of catalytic activity of novel cathode catalyst for fuel cells using polymer-cobalt complexes
AU - Oyaizu, Kenichi
AU - Ikkanda, Koji
AU - Kitao, Mizuki
AU - Tanaka, Ken
AU - Yamaguchi, Aritomo
AU - Yuasa, Makoto
PY - 2005
Y1 - 2005
N2 - Oxidative polymerization of pyrrole onto a surface of a carbon particle dispersed in an electrolyte solution was performed using a fluid-bed electrode where the carbon particle served as a working electrode. Complexation of the polypyrrole (PPy)-modified carbon particle with a cobalt ion by a heterogeneous process proceeded irreversibly and almost quantitatively to give a Co-PPy complex-modified carbon particle, which proved to be a good catalyst for the electro-reduction of oxygen. Voltammetric analysis using an electrode modified with a Nafion film containing the catalyst revealed that oxygen was reduced by four electrons at a high peak potential. Heat treatment of the catalyst greatly improved the catalytic activity. The improvement in the activity was ascribed to the decrease in the size of the active site, which led to a closer packing of the catalyst at the carbon surface. The high activity and the stability suggested that the catalyst can be used as an alternative to the conventional Pt/C catalyst in fuel cells. This is an abstract of a paper presented at the 229th ACS National Meeting (San Diego, CA 3/13-17/2005).
AB - Oxidative polymerization of pyrrole onto a surface of a carbon particle dispersed in an electrolyte solution was performed using a fluid-bed electrode where the carbon particle served as a working electrode. Complexation of the polypyrrole (PPy)-modified carbon particle with a cobalt ion by a heterogeneous process proceeded irreversibly and almost quantitatively to give a Co-PPy complex-modified carbon particle, which proved to be a good catalyst for the electro-reduction of oxygen. Voltammetric analysis using an electrode modified with a Nafion film containing the catalyst revealed that oxygen was reduced by four electrons at a high peak potential. Heat treatment of the catalyst greatly improved the catalytic activity. The improvement in the activity was ascribed to the decrease in the size of the active site, which led to a closer packing of the catalyst at the carbon surface. The high activity and the stability suggested that the catalyst can be used as an alternative to the conventional Pt/C catalyst in fuel cells. This is an abstract of a paper presented at the 229th ACS National Meeting (San Diego, CA 3/13-17/2005).
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M3 - Conference article
AN - SCOPUS:22744455287
SN - 0065-7727
VL - 229
SP - ANYL-102
JO - ACS National Meeting Book of Abstracts
JF - ACS National Meeting Book of Abstracts
IS - 1
T2 - 229th ACS National Meeting
Y2 - 13 March 2005 through 17 March 2005
ER -