材料科学
再分配(选举)
阳极
金属
枝晶(数学)
化学物理
离子
分子动力学
化学工程
纳米技术
冶金
物理化学
计算化学
电极
有机化学
工程类
物理
政治
化学
数学
政治学
法学
几何学
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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