On the Influence of Oxygen on the Degradation of Fe-N-C Catalysts.
Kavita KumarLaetitia DubauMichel MermouxJingkun LiAndrea ZitoloJaysen NelayahFrédéric JaouenFrédéric M MaillardPublished in: Angewandte Chemie (International ed. in English) (2020)
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 O2 - vs. Ar-saturated pH 1 electrolyte. Raman spectroscopy results show carbon corrosion after AST in O2 , even when cycling at low potentials, while no corrosion occurred after any load cycling AST in Ar. The load-cycling AST in O2 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 O2 is due to reactive oxygen species produced between H2 O2 and Fe sites via Fenton reactions.
Keyphrases
- metal organic framework
- induced apoptosis
- highly efficient
- raman spectroscopy
- high intensity
- reactive oxygen species
- cell cycle arrest
- aqueous solution
- ionic liquid
- transition metal
- magnetic resonance imaging
- oxidative stress
- hydrogen peroxide
- multidrug resistant
- genome wide
- risk assessment
- dna methylation
- solid state
- dual energy
- solid phase extraction
- human health