电解质
阴极
共晶体系
阴极保护
深共晶溶剂
材料科学
电极
溶剂
相(物质)
阳极
化学工程
无机化学
化学
冶金
合金
有机化学
物理化学
工程类
作者
Fang Xian,Jiedong Li,Zhenglin Hu,Qian Zhou,Chen Wang,Chenglong Lu,Zhongyi Zhang,Shanmu Dong,Chunbo Mou,Guanglei Cui
摘要
The limited discharge capacity of LiCoO2 can be improved by increasing its working potential, but it suffers from Co4+ dissolution and decomposition of the electrolyte. Nitriles have attracted great interest as high-voltage electrolytes due to their wide electrochemical window. However, the cathodic interfacial stability of nitrile electrolytes with a high-voltage LiCoO2 cathode has yet to be explored. Herein, we adopted an SN-based deep eutectic electrolyte with SN as the only solvent and found that Co4+ could be reduced by the SN solvent on the interface of the LiCoO2 electrode, causing a reverse phase change of LiCoO2 and severe self-discharge of the LiCoO2|Li and LiCoO2|Li4Ti5O12 batteries. When LiDFOB was introduced into the electrolyte, the self-discharge behavior of cells could be largely decelerated. The series of characterizations performed in our work revealed that the cathode/electrolyte interface generated from the LiDFOB salt could stabilize the interface of LiCoO2 and suppress the dissolution of the ions of the transition metal Co.
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