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Elucidating the mechanism of the oxygen reduction reaction for pyrolyzed Fe-N-C catalysts in basic media

Authors :
César Zúñiga
Christian Candia-Onfray
Ricardo Venegas
Karina Muñoz
Jonathan Urra
María Sánchez-Arenillas
José F. Marco
José H. Zagal
Francisco J. Recio
Source :
Electrochemistry Communications, Vol 102, Iss , Pp 78-82 (2019)
Publication Year :
2019
Publisher :
Elsevier, 2019.

Abstract

The study of non-precious metal catalysts (NPMCs) as alternatives to platinum for oxygen reduction is crucial if the use of fuel cells is to become more widespread. Among NPMCs, pyrolyzed catalysts (Fe-N-C) are particularly promising in both basic and acid media. The characterization of active sites and the understanding of the oxygen reduction reaction (ORR) mechanism are crucial for the design of active Fe-N-C catalysts. In this study, we have tested the involvement of the metal centre in the ORR process at pH 13 for two pyrolyzed iron porphyrins. The pyrolyzed catalysts present a FeN4 active site structure similar to that of the porphyrin precursors. Regarding the mechanism, we have found evidence for the crucial role of the Fe(II) centres. There is a direct relation between the Fe(III)/(II) redox transition of the catalysts and the onset potential of the ORR, showing that the electrogeneration of Fe(II) from Fe(III)OH– controls the catalysis. The poisoning of iron centres with CN− induces a decrease in the ORR activity. However, the onset potential for H2O2 generation remains unchanged. The Tafel plots show two different slopes at high and low overpotentials. Based on these results, we propose two different mechanisms, both dependent on the redox potential of the catalysts and the FeO2 binding energy. Keywords: Oxygen reduction reaction, Mechanism, Pyrolyzed catalysts, Redox potential, Cyanide poisoning

Details

Language :
English
ISSN :
13882481
Volume :
102
Issue :
78-82
Database :
Directory of Open Access Journals
Journal :
Electrochemistry Communications
Publication Type :
Academic Journal
Accession number :
edsdoj.92b972a3eb024d2a8f74440c92d1f161
Document Type :
article
Full Text :
https://doi.org/10.1016/j.elecom.2019.04.005