ZIFs‐Derived Hollow Nanostructures via a Strong/Weak Coetching Strategy for Long‐Life Rechargeable Zn–Air Batteries

Abstract Recently, zeolitic imidazolate frameworks (ZIFs) composites have emerged as promising precursors for synthesizing hollow‐structured N‐doped carbon‐based noble‐metal materials with diverse structures and compositions. Here, a strong/weak competitive coordination strategy is presented for synthesizing high‐performance electrocatalysts with hollow features. During the competitive coordination process, the cubic zeolitic‐imidazole framework‐8 (Cube‐8)@ZIF‐67 with core–shell structures are transformed into Cube‐8@ZIF‐67@PF/POM with yolk–shell nanostructures employing phosphomolybdic acid (POM) and potassium ferricyanide (PF) as the strong chelator and the weak chelator, respectively. After calcination, the hollow Mo/Fe/Co@NC catalyst exhibits superior performance in both oxygen evolution reaction (OER) and oxygen reduction reaction (ORR). Interestingly, the Mo/Fe/Co@NC catalyst exhibits efficient electrocatalytic performance for Zn–air batteries (ZABs), with a high power density (≈150 mW cm −2 ) and superior cycling life (≈500 h) compared to commercial platinum/carbon (Pt/C) and ruthenium dioxide (RuO 2 ) mixture benchmarks catalysts. In addition, the density functional theory further proves that after the introduction of Mo and Fe atoms, the adsorption energy with the adsorption intermediates is weakened by adjusting the d ‐band center, thus weakening the reaction barrier and promoting the reaction kinetics of OER. Undoubtedly, this study presents novel insights into the fabrication of ZIFs‐derived hollow structure bifunctional oxygen electrocatalysts for clean‐energy diverse applications.