Atomically Dispersed Ce Sites Augmenting Activity and Durability of Fe‐Based Oxygen Reduction Catalyst in PEMFC

Abstract

AbstractIn the cathode of proton exchange membrane fuel cells (PEMFCs), Fe and N co‐doped carbon (Fe–N–C) materials with atomically dispersed active sites are one of the satisfactory candidates to replace Pt‐based catalysts. However, Fe–N–C catalysts are vulnerable to attack from reactive oxygen species, resulting in inferior durability, and current strategies failing to balance the activity and stability. Here, this study reports Fe and Ce single atoms coupled catalysts anchored on ZIF‐8‐derived nitrogen‐doped carbon (Fe/Ce–N–C) as an efficient ORR electrocatalyst for PEMFCs. In PEMFC tests, the maximum power density of Fe/Ce–N–C catalyst reached up to 0.82 W cm−2, which is 41% larger than that of Fe–N–C. More importantly, the activity of Fe/Ce–N–C catalyst only decreased by 21% after 30 000 cycles under H2/air condition. Density functional theory reveals that the strong coupling between the Fe and Ce sites result in the redistribution of electrons in the active sites, which optimizes the adsorption of OH* intermediates on the catalyst and increases the intrinsic activity. Additionally, the admirable radical scavenging ability of the Ce sites ensured that the catalysts gained long‐term stability. Therefore, the addition of Ce single atoms provides a new strategy for improving the activity and durability of oxygen reduction catalysts.