电解质
锌
水溶液
分层(种子)
化学
多物理
再分配(选举)
化学工程
材料科学
化学物理
储能
不稳定性
化学能
无机化学
对流
离子
自然对流
作者
Zhongxi Zhao,Yongtang Chen,Yongfu Liu,Jiangfeng Huang,Junshuo Lian,Yaoming Leng,Peng Tan
标识
DOI:10.1021/acsenergylett.6c00171
摘要
The deployment of aqueous zinc batteries in next-generation energy storage is hindered by interfacial instability of the zinc anode, closely linked to the spatiotemporal evolution of interfacial chemical fields. Herein, an in-situ 3D pH visualization platform directly reveals a spontaneous and persistent gravity-aligned pH gradient at the zinc-electrolyte interface, reaching ∼0.6 between the upper and lower regions. Coupled multiphysics simulations show that electrochemically induced electrolyte density stratification drives natural convection, dominating ion and proton transport and sustaining pH and Zn2+ gradients. The resulting vertical chemical stratification spatially decouples interfacial reactions, leading to directional zinc redistribution. As a proof of concept, suppressing convection using a mixed-salt electrolyte homogenizes the interfacial pH (ΔpH < 0.1) and extends the cycling lifetime of symmetric zinc batteries by over 75%. This work reveals a gravity-coupled mechanism governing interfacial chemical field evolution, providing general physical principles for stabilizing aqueous metal anodes.
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