剥离(纤维)
阳极
锌
阴极
透视图(图形)
纳米技术
锌合金
计算机科学
电偶阳极
材料科学
联轴节(管道)
电镀(地质)
破译
储能
电流(流体)
低能
化学
钥匙(锁)
锌化合物
工艺工程
作者
Yanpeng Guo,Biyu Lin,Qikun Zhang,Wen Zhang,Chongbo Zhan,Caicai Li,Xizheng Liu,Tianyou Zhai,Huiqiao Li
标识
DOI:10.1002/adma.202522939
摘要
The quest for stable aqueous zinc metal batteries has rightly focused on taming the unruly nature of zinc deposition. Pioneering research has produced a wealth of strategies to achieve uniform zinc plating. While these methods have significantly improved performance in laboratory half-cells, a stubborn performance gap persists when moving to practical full-cells. This chasm points to a fundamental oversight: the critical impact of the anode's initial stripping in a full-cell configuration with zinc-free cathodes. In this perspective, we highlight the pivotal yet underappreciated role of the initial zinc stripping process. We first decipher the operational protocols of zinc-free cathode systems to illustrate how the initial stripping dynamically reshapes the anode and interface. By analyzing the multi-step complexity of stripping, we contrast its mechanistic disparities with plating and assess the limitations of deposition-centric strategies. We then evaluate current approaches that enhance full-cell performance through optimized dissolution. Finally, looking toward future multi-scenario applications, we argue that research must address the intricate coupling among stripping dynamics, chemo-mechano-thermal responses, and the crystallographic properties of zinc anodes. This paradigm shift from a plating-centric view to a full-cycle-oriented is paramount to unlocking the full potential of the zinc metal anode for grid-scale energy storage and beyond.
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