Oxygen reduction characteristics of graphite electrodes modified with cobalt di-quinolyldiamine derivatives

被引:30
作者
Okada, T
Yoshida, M
Hirose, T
Kasuga, K
Yu, T
Yuasa, M
Sekine, I
机构
[1] AIST, Natl Inst Mat & Chem Res, Tsukuba, Ibaraki 3058565, Japan
[2] Tokyo Univ Sci, Fac Sci & Technol, Dept Ind Chem, Noda, Chiba 2788510, Japan
[3] Saitama Univ, Fac Engn, Dept Appl Chem, Urawa, Saitama 3388570, Japan
[4] Univ Calif Berkeley, Dept Mat Sci & Mineral Engn, Berkeley, CA 94720 USA
关键词
diamine; cobalt; oxygen reduction; pyrolysis; mixed catalyst;
D O I
10.1016/S0013-4686(00)00499-0
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
N,N'-di-8-Quinolyltrimethylenediamine cobalt [Co(dqpr)] and N,N'-di-8-quinolylphenylenediamine cobalt [Co(dqph)] were synthesized and tested as catalysts for electro-reduction of oxygen when immobilized on graphite electrodes. For modification on graphite, the complexes were mixed with graphite powder and heat-treated in Ar atmosphere at 400-800 degrees C, then immobilized on graphite electrode with Nafion solution. The performance was improved significantly by the heat treatment, and it was assumed to be due to the formation of stabilized CoN4 chelate structure still remaining on the graphite surface after pyrolysis. The polarization measurements revealed that the performance of the electrodes modified with the complexes was parallel to that of 5% platinum dispersed on carbon. Durability tests of the heat-treated complex at 80 degrees C in acidic aqueous solutions showed relatively good catalytic performances as oxygen reduction catalysts, as compared with platinum. The potential usage of the complexes was demonstrated as the cathode catalysts in polymer electrolyte fuel cells in combination with fewer amounts of platinum, where a remarkable concerted effect is observed between platinum sites and CoN4 centers dispersed on carbon substrate. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:4419 / 4429
页数:11
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