On the Stability of an Atomically-Dispersed Fe−N−C ORR Catalyst: An In Situ XAS Study in a PEMFC

Abstract

The stability of Fe−N−C oxygen reduction reaction (ORR) electrocatalysts has been considered a primary challenge for their practical application in proton exchange membrane fuel cells (PEMFCs). While several studies have attempted to reveal the possible degradation mechanism of Fe−N−C ORR catalysts, there are few research results reporting on their stability as well as the possible Fe species formed under different voltages in real PEMFC operation. In this work, we employ in-situ X-ray absorption near-edge structure (XANES) to monitor the active-site degradation byproducts of an atomically dispersed Fe−N−C ORR catalyst under a H₂/O₂-operating PEMFC at 90 % relative humidity and 80 °C. For this, stability tests were carried out at two constant cell voltages, namely 0.4 and at 0.8 V. Even though the ORR activity of the Fe−N−C catalyst decreased significantly and was almost identical at the end of the tests for the two voltages employed, the analysis of the XANES recorded under H₂/N₂ configuration at 0.6 and 0.9 V within the stability test suggests that two different degradation mechanisms occur. They are demetalation of iron cations followed by their precipitation into Fe oxides upon operation at 0.8 V, versus a chemical carbon oxidation close to the active sites, likely triggered by reactive oxygen species (ROS) originated from the H₂O₂ formation, during the operation at 0.4 V.