Temperature dependence of oxygen reduction catalyzed by cobalt fluoro-phthalocyanine adsorbed on a graphite electrode

被引:36
作者
Song, C.
Zhang, L.
Zhang, J. [1 ]
Wilkinson, D. P.
Baker, R.
机构
[1] Natl Res Council Canada, Inst Fuel Cell Innovat, Vancouver, BC V6T 1W5, Canada
[2] Univ British Columbia, Dept Chem & Biol Engn, Vancouver, BC V6T 1Z4, Canada
关键词
cobalt phthalocyanine; electro-reduction; fuel cells; hydrogen peroxide; oxygen; temperature dependence;
D O I
10.1002/fuce.200500205
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The graphite electrode surface onto which cobalt(II) 1,2,3,4,8,9, 10,1 1,15,16,17,18,22,23,24,25-hexadecafluoro-29H,31H-phthalocyanine (abbreviated as (CoHFPC)-H-II) is adsorbed displays a strong electrocatalytic activity toward O2 reduction. The electrochemical response of surface adsorbed (CoHFPC)-H-II is investigated at different pHs and temperatures by cyclic voltammetry. The kinetics of the catalyzed O2 reduction at different temperatures, measured by cyclic voltammetric and rotating disk electrode methods, is analyzed and a corresponding reaction mechanism is proposed. A two-electron/two-proton process is found to be the dominating pathway for (CoHFPC)-H-II catalyzed O-2 reduction. The increase in temperature, from 20 to 70 degrees C, enhances the reduction rate significantly. The presence of methanol has no effect on its catalytic activity towards O-2 reduction. The implications of using this non-noble electrocatalyst for the cathode reaction in low temperature fuel cells, including direct organic, metal-air fuel cells, etc., are discussed in this paper.
引用
收藏
页码:9 / 15
页数:7
相关论文
共 39 条
[1]   MECHANISM OF ELECTROCATALYTIC REDUCTION OF OXYGEN ON METAL-CHELATES [J].
ALT, H ;
BINDER, H ;
SANDSTED.G .
JOURNAL OF CATALYSIS, 1973, 28 (01) :8-19
[2]   Novel multinuclear catalysts for the electroreduction of dioxygen directly to water [J].
Anson, FC ;
Shi, CN ;
Steiger, B .
ACCOUNTS OF CHEMICAL RESEARCH, 1997, 30 (11) :437-444
[3]   ELECTROCATALYSIS OF OXYGEN REDUCTION PROCESS ON METAL-CHELATES IN ACID ELECTROLYTE [J].
BAGOTZKY, VS ;
TARASEVICH, MR ;
RADYUSHKINA, KA ;
LEVINA, OA ;
ANDRUSYOVA, SI .
JOURNAL OF POWER SOURCES, 1978, 2 (03) :233-240
[4]  
BARD AJ, 1980, ELECTROCHEMICAL METH
[5]  
BATTINO R, 1979, IUPAC SOLUBILITY DAT, V7
[6]   REDOX MECHANISM OF CHELATE-CATALYZED OXYGEN CATHODE [J].
BECK, F .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1977, 7 (03) :239-245
[7]   The selectivity of oxygen reduction by pyrolysed iron porphyrin supported on carbon [J].
Bouwkamp-Wijnoltz, AL ;
Visscher, W ;
van Veen, JAR .
ELECTROCHIMICA ACTA, 1998, 43 (21-22) :3141-3152
[8]   Novel electrocatalysts for direct methanol fuel cells [J].
Chu, D ;
Jiang, RZ .
SOLID STATE IONICS, 2002, 148 (3-4) :591-599
[9]   TEMPERATURE-DEPENDENCE OF THE TAFEL SLOPE FOR OXYGEN REDUCTION ON PLATINUM IN CONCENTRATED PHOSPHORIC-ACID [J].
CLOUSER, SJ ;
HUANG, JC ;
YEAGER, E .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1993, 23 (06) :597-605
[10]   ELECTRODE CATALYSIS OF THE 4-ELECTRON REDUCTION OF OXYGEN TO WATER BY DICOBALT FACE-TO-FACE PORPHYRINS [J].
COLLMAN, JP ;
DENISEVICH, P ;
KONAI, Y ;
MARROCCO, M ;
KOVAL, C ;
ANSON, FC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1980, 102 (19) :6027-6036