共晶体系
电解质
离子电导率
锂(药物)
电导率
材料科学
化学工程
法拉第效率
离子
无机化学
化学
有机化学
冶金
电极
物理化学
合金
工程类
医学
内分泌学
作者
Jiahan Song,Yubing Si,Wei Guo,Donghai Wang,Yongzhu Fu
标识
DOI:10.1002/anie.202016875
摘要
Abstract Deep eutectic electrolytes (DEEs) are a new class of electrolytes with unique properties. However, the intermolecular interactions of DEEs are mostly dominated by Li⋅⋅⋅O interactions, limiting the diversity of chemical space and material constituents. Herein, we report a new class of DEEs induced by Li⋅⋅⋅N interactions between 2,2′‐dipyridyl disulfide (DpyDS) and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI). The strong ion‐dipole interaction triggers the deep eutectic phenomenon, thus liberating the Li + from LiTFSI and endowing the DEEs with promising ionic conductivity. These DEEs show admirable intrinsic safety, which cannot be ignited by flame. The DEE at the molar ratio of DpyDS:LiTFSI=4:1 (abbreviated as DEE‐4:1) is electrochemically stable between 2.1 and 4.0 V vs. Li/Li + , and exhibits an ionic conductivity of 1.5×10 −4 S cm −1 at 50 °C. The Li/LiFePO 4 half cell with DEE‐4:1 can provide a reversible capacity of 130 mAh g −1 and Coulombic efficiency above 98 % at 50 °C.
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