锌
阳极
水溶液
电解质
溶解
枝晶(数学)
电偶阳极
动力学
螯合作用
电化学
化学工程
材料科学
化学
无机化学
电极
冶金
有机化学
物理化学
数学
几何学
工程类
量子力学
物理
阴极保护
作者
Shan Cai,Jiugang Hu,Yuqing Luo,Pengfei Zhu,Ting He,Hongshuai Hou,Guoqiang Zou,Xiaobo Ji
标识
DOI:10.1016/j.cej.2022.140145
摘要
Severe side reactions and dendrite growth are widespread in zinc anodes due to the aqueous electrolyte and the inhomogeneity of the Zn surface. Constructing an artificial interfacial layer on the zinc anode is a direct and effective strategy to solve these problems. Herein, a dithio-bridged chelate (DTBC) network consisting of zinc dimethyldithiocarbamate molecules was in situ constructed on the zinc surface via a facile interfacial dissolution-coordination strategy. The experiment and theoretical calculation revealed that the DTBC network simultaneously improves the thermos-kinetics properties of zinc anode. Moreover, the dithio groups in the DTBC network can induce the preferred plating of Zn along the (0 0 2) crystal plane and suppress dendrite growth. The DTBC-Zn electrode delivered an extended lifetime of over 1200 h with an ultralow polarization of ∼27.3 mV at 0.5 mA cm−2. The capacity retention rate of DTBC-Zn|MnO2 full cell was as high as 97.98 % after 1600 cycles, further confirming the feasibility of the robust dithio-bridged chelate network for stabilizing thermo-kinetics of zinc anode. This work contributes a simple and effective way to construct high-performance zinc anodes for aqueous zinc ion batteries.
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