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

被引:240
作者
Kumar, Kavita [1 ]
Dubau, Laetitia [1 ]
Mermoux, Michel [1 ]
Li, Jingkun [2 ]
Zitolo, Andrea [3 ]
Nelayah, Jaysen [4 ]
Jaouen, Frederic [2 ]
Maillard, Frederic [1 ]
机构
[1] Univ Grenoble Alpes, Univ Savoie Mt Blanc, CNRS, Grenoble INP,LEPMI, F-38000 Grenoble, France
[2] Univ Montpellier, Inst Charles Gerhardt Montpellier, CNRS, ENSCM,UMR 5253, 2 Pl Eugene Bataillon, F-34095 Montpellier, France
[3] Synchrotron SOLEIL, BP 48 St Aubin, F-91192 Gif Sur Yvette, France
[4] Univ Paris, CNRS, Lab Mat & Phenomenes Quant, F-75013 Paris, France
关键词
carbon corrosion; Fe-N-C Catalysts; oxygen reduction reaction; polymer electrolyte membrane fuel cells; reactive oxygen species (ROS); REDUCTION REACTION; ACTIVE-SITES; FE/N/C CATALYSTS; METAL-CATALYSTS; STABILITY; IRON; PEROXIDE;
D O I
10.1002/anie.201912451
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:3235 / 3243
页数:9
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