成核
锌
材料科学
阳极
电解质
枝晶(数学)
电偶阳极
电化学
水溶液
电磁屏蔽
化学工程
纳米技术
电池(电)
阴极
电化学窗口
屏蔽效应
冶金
化学
复合材料
电极
阴极保护
有机化学
物理化学
离子电导率
功率(物理)
工程类
物理
量子力学
数学
几何学
作者
Yi Yuan,Shengda D. Pu,Miguel A. Pérez‐Osorio,Zixuan Li,Shengming Zhang,Sixie Yang,Boyang Liu,Gong Chen,Ashok S. Menon,Louis F. J. Piper,Xiangwen Gao,Peter G. Bruce,Alex W. Robertson
标识
DOI:10.1002/adma.202307708
摘要
Aqueous zinc electrolytes offer the potential for cheaper rechargeable batteries due to their safe compatibility with the high capacity metal anode; yet, they are stymied by irregular zinc deposition and consequent dendrite growth. Suppressing dendrite formation by tailoring the electrolyte is a proven approach from lithium batteries; yet, the underlying mechanistic understanding that guides such tailoring does not necessarily directly translate from one system to the other. Here, it is shown that the electrostatic shielding mechanism, a fundamental concept in electrolyte engineering for stable metal anodes, has different consequences for the plating morphology in aqueous zinc batteries. Operando electrochemical transmission electron microscopy is used to directly observe the zinc nucleation and growth under different electrolyte compositions and reveal that electrostatic shielding additive suppresses dendrites by inhibiting secondary zinc nucleation along the (100) edges of existing primary deposits and encouraging preferential deposition on the (002) faces, leading to a dense and block-like zinc morphology. The strong influence of the crystallography of Zn on the electrostatic shielding mechanism is further confirmed with Zn||Ti cells and density functional theory modeling. This work demonstrates the importance of considering the unique aspects of the aqueous zinc battery system when using concepts from other battery chemistries.
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