This study demonstrates that a novel Fe2P/SbZn heterostructure enhances oxygen reduction reaction in zinc–air batteries, suggesting improved efficiency.
The strategic construction of heterostructures centered around Fe 2 P is proven to be effective for improving its performance in the oxygen reduction reaction (ORR) and zinc–air batteries (ZABs). In this study, SbZn is strategically employed to construct a novel Fe 2 P/SbZn heterostructure on N,P‐doped carbon scaffolds, serving as an efficient electrocatalyst for the ORR in ZABs. Through a one‐step pyrolysis of a Fe, Sb, P‐incorporated zeolitic imidazolate framework, the Fe 2 P/SbZn@PNC catalyst is successfully synthesized. This catalyst demonstrates high ORR activity in alkaline media, achieving a half‐wave potential of 0.936 V and a limiting current density of 6.18 mA cm −2 , both significantly surpassing those of commercial 20 wt% Pt/C. When applied in zinc–air batteries, the Fe 2 P/SbZn@PNC‐based ZABs deliver a higher peak power density and superior long‐term cycling stability compared to the Pt/C benchmark. Density functional theory (DFT) calculations reveal that the Fe 2 P/SbZn interface drives charge redistribution, optimizing the adsorption/desorption of oxygen intermediates and reducing the rate‐determining energy barrier in ORR, thus enhancing catalytic activity. This innovative heterostructure provides new avenues for designing efficient electrocatalysts for energy conversion and storage.
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Guo et al. (2025) studied this question.
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