材料科学
再分配(选举)
法拉第效率
过电位
电解质
阳极
金属
阴极
成核
吸附
无机化学
离子
缓冲器(光纤)
化学工程
动能
氢
钾
阴极保护
降级(电信)
作者
Canglong Li,Fangyan Liu,Hiroshi Yao,Tiancheng You,Lu Wang,Shaozhen Huang,Jiaqi Huang,Han Wang,Yuejiao Chen,Libao Chen,Guanghui Li
标识
DOI:10.1002/adfm.202514260
摘要
Abstract Aqueous Zn ion batteries suffer from irreversible anode degradation caused by hydrogen evolution reaction (HER)‐driven electrolyte alkalization and non‐uniform Zn deposition. Here, a bi‐functional buffer additive is proposed that synergistically couples pH regulation and interfacial ion‐redistribution. The buffer additive maintains electrolyte with a self‐regulated pH (≈3) through proton donor‐acceptor equilibria, effectively scavenging hydroxyl ions to prevent Zn passivation, while inducing preferential Na⁺ adsorption at protrusions to enforce planar Zn deposition via charge screening effects. This dual mechanism enables an ultralow nucleation overpotential (24.5 mV) and an ultrahigh Coulombic efficiency (99.9% over 12 000 cycles) in Cu–Zn half cells. Full cells with NaV 3 O 8 cathodes achieve 93% capacity retention after 3000 cycles at 10 A g −1 , while pouch cells (20.89 mg cm −2 cathode) retain 81.6% capacity over 300 cycles at 1 A g −1 . This work establishes a universal paradigm for stabilizing Zn anodes through coupled thermodynamic and kinetic regulation, positioning Zn‐ion batteries as viable candidates for grid‐scale energy storage.
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