摘要
Flexible zinc-air batteries (ZABs) are promising power sources for wearable and portable electronics owing to their high energy density, intrinsic safety, and low cost. However, their practical application remains limited by the sluggish kinetics of oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) at the air cathode. Here, we develop a plasma-driven one-step exsolution-sulfidation strategy to construct CoS 2 /perovskite heterostructures on Sr 1.8 Fe 0.5 Mo 0.5 CoO 6-δ (SFMC) nanofibers. During plasma treatment, Co species are exsolved from the SFMC lattice and simultaneously sulfurized, forming CoS 2 nanoparticles that are firmly anchored on the oxygen-deficient SFMC surface. Experimental results and density functional theory calculations demonstrate that the SFMC/CoS 2 heterointerface induces interfacial charge redistribution, accelerates charge transfer, and lowers the free-energy barriers of OER and ORR. SFMC/CoS 2 exhibits markedly enhanced bifunctional oxygen electrocatalytic activity and enables an all-solid-state flexible ZAB with a peak power density of 247.7 mW cm −2 and robust cycling stability. This work establishes plasma-driven exsolution-sulfidation as an effective strategy for constructing strongly coupled metal sulfide/perovskite heterostructures for high-performance flexible metal-air batteries. A plasma-driven one-step exsolution-sulfidation strategy constructs strongly coupled CoS 2 /perovskite heterostructures, synergistically boosting bifunctional ORR/OER kinetics for high-performance flexible zinc-air batteries. Download: Download high-res image (190KB) Download: Download full-size image
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