化学
阴极
催化作用
氧气
金属
燃料电池
化学工程
化学键
化学稳定性
膜
氮气
无机化学
电流密度
氧还原反应
甲醇
粘结长度
电子
化学反应
反应条件
电极
键裂
氧化还原
电化学
失真(音乐)
作者
Yan Yan,Dongping Xue,Mingkai Liu,Jiawei Duan,Tianyu Gong,Yue Yu,Song Xue,Xinduo Wei,Lintao Jiang,Su Jiang,Guohong Fan,Hui Li,Jianan Zhang,Jie Zeng
摘要
Abstract Proton-exchange membrane fuel cells (PEMFCs) require efficient and durable platinum-group-metal-free (PGM-free) cathode catalysts for the oxygen reduction reaction (ORR). Iron–nitrogen–carbon (Fe–N–C) materials are promising candidates, but their practical application is hindered by rapid demetalation of Fe sites under acidic operating conditions. Here, we show that introducing a p-block metal (Bi) adjacent to the FeN4 motif triggers a pseudo-Jahn–Teller (p-J-T) distortion. This distortion stabilizes a medium-spin Fe(III) configuration (S = 3/2) with an empty dx2–y2 orbital. This empty orbital accepts lone-pair electrons from the nitrogen ligands, strengthening the Fe–N bond and suppressing proton-induced demetalation. The resulting FeBi–N–C catalyst exhibits a dramatically strengthened Fe–N bond, as evidenced by a shortened bond length (from 1.99 Å to 1.96 Å) and a 3-fold higher Fe retention after 20,000 cycles (78.8% vs 26.7%). This structural stability translates into a peak power density of 720 mW cm–2 in H2–O2 PEMFCs and 90% current retention after 150 h at 0.60 V. Our findings establish the p-J-T effect as a new chemical strategy to stabilize metal–nitrogen bonds against acid-induced demetalation.
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