材料科学
枝晶(数学)
化学工程
电镀(地质)
阳极
锌
水溶液
剥离(纤维)
电解质
电化学窗口
法拉第效率
离子电导率
无机化学
电极
复合材料
冶金
有机化学
化学
几何学
物理化学
工程类
地质学
数学
地球物理学
作者
Junnan Hao,Xiao‐Long Li,Shilin Zhang,Fuhua Yang,Xiaohui Zeng,Shuai Zhang,Guyue Bo,Chunsheng Wang,Zaiping Guo
标识
DOI:10.1002/adfm.202001263
摘要
Abstract Zn metal has been regarded as the most promising anode for aqueous batteries due to its high capacity, low cost, and environmental benignity. Zn anode still suffers, however, from low Coulombic efficiency due to the side reactions and dendrite growth in slightly acidic electrolytes. Here, the Zn plating/stripping mechanism is thoroughly investigated in 1 m ZnSO 4 electrolyte, demonstrating that the poor performance of Zn metal in mild electrolyte should be ascribed to the formation of a porous by‐product (Zn 4 SO 4 (OH) 6 · x H 2 O) layer and serious dendrite growth. To suppress the side reactions and dendrite growth, a highly viscoelastic polyvinyl butyral film, functioning as an artificial solid/electrolyte interphase (SEI), is homogeneously deposited on the Zn surface via a simple spin‐coating strategy. This dense artificial SEI film not only effectively blocks water from the Zn surface but also guides the uniform stripping/plating of Zn ions underneath the film due to its good adhesion, hydrophilicity, ionic conductivity, and mechanical strength. Consequently, this side‐reaction‐free and dendrite‐free Zn electrode exhibits high cycling stability and enhanced Coulombic efficiency, which also contributes to enhancement of the full‐cell performance when it is coupled with MnO 2 and LiFePO 4 cathodes.
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