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Heat-treated iron(III) tetramethoxyphenyl porphyrin chloride supported on high-area carbon as an electrocatalyst for oxygen reduction: Part II. Kinetics of oxygen reduction

Oxygen reduction was investigated at FeTMPP–Cl adsorbed on the Black Pearls carbon and heat-treated at temperatures from 200 to 1000°C. Kinetic parameters of the reaction and the dependence of the reaction rate on the heat-treatment temperature were established in acid and alkaline media. It was fou...

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Bibliographic Details
Published in:Journal of electroanalytical chemistry (Lausanne, Switzerland) Switzerland), 1999-02, Vol.462 (1), p.63-72
Main Authors: Gojković, S.Lj, Gupta, S, Savinell, R.F
Format: Article
Language:English
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Summary:Oxygen reduction was investigated at FeTMPP–Cl adsorbed on the Black Pearls carbon and heat-treated at temperatures from 200 to 1000°C. Kinetic parameters of the reaction and the dependence of the reaction rate on the heat-treatment temperature were established in acid and alkaline media. It was found that the O 2 reduction rate increases with increase in the heat-treatment temperature of the electrocatalyst, reaching a plateau at 700≤ T≤1000°C. The reaction rate was higher in alkaline solution on all electrocatalysts examined, but its dependence on the heat-treatment temperature was the same as in acid media. Like similar other macrocycle catalysts, FeTMPP–Cl/BP was found to be methanol-tolerant. The effect of sulfate, perchlorate, and phosphate anions was also investigated and no influence on the reaction rate was found. Activities of FeTMPP–Cl/BP and Pt/BP electrocatalysts were compared. FeTMPP–Cl/BP heat-treated at 700≤ T≤1000°C showed similar activity to Pt/BP if they are compared in alkaline solution, but in acid solution, the reaction rate on the Pt electrocatalyst was higher. The controversy in the literature on the role of metallic Fe particles in O 2 reduction catalysis is discussed. Comparison of present results with previous cyclic voltammetry and TEM investigations of the same electrocatalyst gave further evidence that some other products of the heat-treatment are responsible for the high activity of the catalyst.
ISSN:1572-6657
1873-2569
DOI:10.1016/S0022-0728(98)00390-8