共晶体系
锂(药物)
金属锂
电解质
材料科学
金属
无机化学
化学工程
冶金
化学
合金
物理化学
电极
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
出处
期刊:PubMed
日期:2025-08-10
卷期号:: e202511772-e202511772
标识
DOI:10.1002/anie.202511772
摘要
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 Li3N 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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