化学
电解质
阳极
乙醚
聚合
锂(药物)
法拉第效率
氧化还原
无机化学
化学稳定性
金属锂
化学工程
双层
酰亚胺
锂电池
金属
电池(电)
腐蚀
电化学
二甲醚
溶剂
有机化学
离子键合
化学反应
二聚体
作者
Peter-Paul R.M.L. Harks,Seongjae Ko,Wenxuan Zhao,Fang Zhong,Yaobin Xu,Hong-EE Kim,Xia Cao,Norio Takenaka,Hao Yu,Jie Xiao,Atsuo Yamada
摘要
Lithium metal is regarded as the ideal anode material for rechargeable batteries due to its exceptionally high theoretical capacity and low redox potential. Electrolytes combining imide salts and ethers have been extensively studied for their high reduction stability and ability to form robust protective films on Li-metal surfaces. Despite these advantages, concerns over safety and possible corrosion of battery components may severely limit industrial adoption. A major breakthrough would be the utilization of the well-established LiPF6 salt; however, its chemical instability and tendency to polymerize ether solvents present challenges. Herein, we report LiPF6/ether-based electrolytes that effectively suppress ether polymerization and form highly functional inorganic-organic bilayer films on Li. Consequently, a Coulombic efficiency of 99.5%, which is comparable to those of state-of-the-art imide-based systems, was achieved without using fluorinated solvents or additives. This marks a step forward in advancing LiPF6-based electrolytes for future rechargeable batteries.
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