电解质
材料科学
锂(药物)
电化学窗口
离子电导率
溶剂化
金属锂
枝晶(数学)
无机化学
盐(化学)
化学工程
金属
相间
离子键合
电池(电)
电化学
离子
电极
化学
有机化学
物理化学
热力学
冶金
内分泌学
数学
工程类
功率(物理)
物理
生物
医学
几何学
遗传学
作者
Nan Piao,Xiao Ji,Hong Xu,Xiulin Fan,Long Chen,Sufu Liu,Mounesha N. Garaga,Steve Greenbaum,Li Wang,Chunsheng Wang,Xiangming He
标识
DOI:10.1002/aenm.201903568
摘要
Abstract Development of electrolytes that simultaneously have high ionic conductivity, wide electrochemical window, and lithium dendrite suppression ability is urgently required for high‐energy lithium‐metal batteries (LMBs). Herein, an electrolyte is designed by adding a countersolvent into LiFSI/DMC (lithium bis(fluorosulfonyl)amide/dimethyl carbonate) electrolytes, forming countersolvent electrolytes, in which the countersolvent is immiscible with the salt but miscible with the carbonate solvents. The solvation structure and unique properties of the countersolvent electrolyte are investigated by combining electroanalytical technology with a Molecular Dynamics simulation. Introducing the countersolvent alters the coordination shell of Li + cations and enhances the interaction between Li + cations and FSI − anions, which leads to the formation of a LiF‐rich solid electrolyte interphase, arising from the preferential reduction of FSI − anions. Notably, the countersolvent electrolyte suppresses Li dendrites and enables stable cycling performance of a Li||NCM622 battery at a high cut‐off voltage of 4.6 V at both 25 and 60 °C. This study provides an avenue to understand and design electrolytes for high‐energy LMBs in the future.
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