材料科学
电偶阳极
锌
离子
阳极
阴极
化学工程
电极
电解质
电化学
纳米技术
无机化学
电池(电)
光电子学
冶金
阴极保护
电气工程
物理化学
有机化学
化学
工程类
作者
Yuwei Chen,Jianbo Li,Shimeng Zhang,Junya Cui,Mingfei Shao
标识
DOI:10.1002/admi.202000510
摘要
Abstract Zinc‐ion batteries (ZIBs) have attracted considerable attention and global interest due to their high gravimetric and high volumetric capacities (820 mAh g−1 and 5855 mAh cm−3). However, the Zn protrusions/dendrites during the plating/stripping process of Zn (Zn2+) severely affect the performance of Zn anode, causing a low Coulombic efficiency, rapid degradation of capacity, and even failure of Zn‐anode‐based batteries. In order to reduce the dendritic deposition of Zn, the key is to adjust the initial uniform nucleation, which determines the subsequent uniform deposition of Zn. Herein, a cathode material (MnO2) ultrathin film is first modified on the surface of the carbon cloth as active sites for the in situ nucleation and directed epitaxial growth of metal Zn. As a result, the CC@MnO2‐UTF@Zn anode can be cycled in aqueous electrolyte and maintain stable cycling performance during repeated Zn deposition/stripping processes. Subsequently, the CC@MnO2‐UTF@Zn anode and CC@MnO2 cathode are assembled into full cells, which deliver a superior electrochemical performance. Moreover, the flexible solid‐state ZIBs with the CC@MnO2‐UTF@Zn anode show excellent capacities and high energy/power densities, which is superior to the most reported results so far. This work provides a new strategy to design an advanced flexibility Zn anode toward future high‐performance wearable electronic ZIBs.
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