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Abstract 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 .
Zhao et al. (Tue,) studied this question.