4.8 Article

On the Influence of Oxygen on the Degradation of Fe-N-C Catalysts

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 59, Issue 8, Pages 3235-3243

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201912451

Keywords

carbon corrosion; Fe-N-C Catalysts; oxygen reduction reaction; polymer electrolyte membrane fuel cells; reactive oxygen species (ROS)

Funding

  1. Centre of Excellence of Multifunctional Architectured Materials CEMAM [ANR-10-LABX-44-01]
  2. Region Ile-de-France [SESAME E1845]
  3. French National Research Agency through the CAT2CAT project [ANR-16-CE05-0007]
  4. French National Research Agency through the ANIMA project [ANR-19-CE05-0039]
  5. Synchrotron SOLEIL (Gif-sur Yvette, France) [20171318]
  6. Agence Nationale de la Recherche (ANR) [ANR-16-CE05-0007] Funding Source: Agence Nationale de la Recherche (ANR)

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Fe-N-C catalysts containing atomic FeNx sites are promising candidates as precious-metal-free catalysts for oxygen reduction reaction (ORR) in proton exchange membrane fuel cells. The durability of Fe-N-C catalysts in fuel cells has been extensively studied using accelerated stress tests (AST). Herein we reveal stronger degradation of the Fe-N-C structure and four-times higher ORR activity loss when performing load cycling AST in O-2- vs. Ar-saturated pH 1 electrolyte. Raman spectroscopy results show carbon corrosion after AST in O-2, even when cycling at low potentials, while no corrosion occurred after any load cycling AST in Ar. The load-cycling AST in O-2 leads to loss of a significant fraction of FeNx sites, as shown by energy dispersive X-ray spectroscopy analyses, and to the formation of Fe oxides. The results support that the unexpected carbon corrosion occurring at such low potential in the presence of O-2 is due to reactive oxygen species produced between H2O2 and Fe sites via Fenton reactions.

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