Insight into the Mechanism of Axial Ligands Regulating the Catalytic Activity of Fe–N 4 Sites for Oxygen Reduction Reaction

• Published in: Advanced energy materials Vol. 12; no. 11
• Main Authors: Zhao, Kuang‐Min, Liu, Suqin, Li, Yu‐Yang, Wei, Xianli, Ye, Guanying, Zhu, Weiwei, Su, Yuke, Wang, Jue, Liu, Hongtao, He, Zhen, Zhou, Zhi‐You, Sun, Shi‐Gang
• Format: Journal Article
• Language: English
• Published: 01.03.2022
• ISSN: 1614-6832; 1614-6840
• DOI: 10.1002/aenm.202103588

Identifying the actual structure and tuning the catalytic activity of Fe–N 4 ‐based moieties, well‐recognized high‐activity sites in the oxygen reduction reaction (ORR) are challenging problems. Herein, by using poly(iron phthalocyanine) (PFePc) as an Fe–N 4 ‐based model electrocatalyst, a mechanistic insight into the effect of axial ligands on the ORR catalytic activity of Fe–N 4 is provided and it is revealed that the ORR activity of Fe–N 4 sites with OH desorption as a rate‐determining step is related to the energy level gap between the OH p x p y and Fe 3, which can be tuned by regulating the field strength of the axial ligands. Thus, PFePc coordinated with a weak‐field ligand I − (PFePc‐I) with a low energy level of Fe 3 exhibits high activity evidenced by an ORR half‐wave potential as high as 0.948 V versus RHE. This work develops a novel strategy for tuning the ORR activity of Fe–N 4 and reveals the correlation between the electronic/geometric structure and catalytic activity of Fe–N 4 .