材料科学
分离器(采油)
阳极
水溶液
阴极
离子键合
惰性
聚合物
化学工程
离子
双水相体系
离子液体
纳米技术
电极
离子电导率
储能
相(物质)
腐蚀
锂离子电池的纳米结构
作者
Mei Han,Jian Zhi,Zhongyi Liu,Kaihang Yue,Shaopeng Li,Weinan Zhao,K. J. Ren,Rui Zhu,Pu Chen
标识
DOI:10.1002/aenm.202505800
摘要
ABSTRACT Aqueous Zn//MnO 2 batteries hold significant promise for safe and cost‐effective large‐scale energy storage, yet their practical deployment is hindered by rapid performance degradation. Here, we identify bilateral ionic crosstalk, a previously overlooked failure mechanism driven by active ion, as a root cause of electrode degradation. We demonstrate that excess Zn 2+ migrating from the anode induces irreversible phase transitions at the MnO 2 cathode, forming electrochemically inert Zn x (MnO 2 ) y phase (ZMO sclerosis). Concurrently, dissolved Mn 2+ from the cathode exacerbates corrosion and dendrite growth on the Zn anode. To mitigate this crosstalk, we design a hierarchical fluorinated polymer separator (HFPS). Such HFPS enables selective cation coordination and guides ion transport, achieving simultaneous regulation of Zn 2+ and Mn 2+ fluxes. This targeted regulation effectively mitigates ionic crosstalk and stabilizes both electrodes. Batteries employing the HFPS exhibit exceptional cycling stability, retaining 97% capacity after 1,000 cycles at 0.5 A g −1 with stable operation exceeding 500 h. This performance represents a 54% lifespan enhancement over state‐of‐the‐art aqueous counterparts. Our work provides a fundamental mechanistic understanding of active‐ion‐induced failure and establishes ion flux regulation as a universal design strategy for durable aqueous zinc‐ion batteries.
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