共晶体系
锂(药物)
电解质
硝酸锂
材料科学
离子键合
无机化学
离子
化学工程
化学
合金
物理化学
电极
有机化学
工程类
医学
内分泌学
作者
Xiaosheng Song,Yi Zhang,Zhijie Guo,Shuang Wu,Yong Zhao,Xinghui Liang,Myoung‐Chan Kim,Hun Kim,Yang‐Kook Sun
标识
DOI:10.1002/anie.202511772
摘要
Abstract Achieving long‐term cycling stability in high‐temperature lithium metal batteries (LMBs) demands both efficient ion transport and stable electrode interfaces. However, the molecular polarity and strong ionic interactions of conventional electrolytes hinder ion mobility and compromise interfacial stability. In this study, we developed a deep eutectic electrolyte based on Li‐bond (Li‐DEE) comprising tetraethylammonium nitrate and lithium bis(fluorosulfonyl)imide, which is different from the traditional hydrogen bonding or lithium ionic bonding electrolyte. The Li‐bond network within the Li‐DEE enables rapid lithium‐ion transport (6.5 × 10 − 3 S cm −1 at 100 °C) while forming a stable electrode interface rich in Li 3 N and LiF. As a result, the Li‐DEE enables an LMB to deliver a high capacity retention of 80% over 635 cycles at 0.5 C and a capacity of 84.4 mAh g −1 after 1500 cycles at 2 C and 100 °C. This study provides valuable insights for designing next‐generation electrolytes that function under extreme operating conditions.
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