材料科学
电解质
离子电导率
阳极
聚合物
共晶体系
化学工程
阴极
电导率
金属锂
电极
锂(药物)
离子键合
无机化学
吸附
有机自由基电池
溶剂化
电池(电)
快离子导体
离子
金属
深共晶溶剂
导电聚合物
电化学窗口
高分子化学
锂电池
锂离子电池的纳米结构
相容性(地球化学)
分离器(采油)
储能
锂离子电池
溶剂
作者
Dashan Zhang,Ting Tian,Yu Guo,Jikai Zhang,Junwei An,Hui Jia,Yongzheng Shi,Peter Müller‐Buschbaum,Shubin Yang,Bin Li
标识
DOI:10.1002/adfm.202524041
摘要
Abstract Polymer electrolytes (PEs) are attractive due to their lightweight, flexibility, facile processability, and intimate solid–solid contact with electrodes for solid‐state lithium‐metal batteries (LMBs). Unfortunately, their practical application is impeded by insufficient ionic conductivity and an unstable electrolyte/electrode interface. Herein, by integrating a butadiene sulfone‐based deep‐eutectic solvent with a fluorinated polymer matrix (PVDF‐HFP), a deep eutectic polymer electrolyte (DEPE) is developed. It is demonstrated that the butadiene sulfone not only liberates lithium ions from the C‐F dipoles in polymer chains, but also establishes a contact‐ion‐pair‐dominated solvation structure, resulting in the DEPE with a high ionic conductivity of 2.1 × 10 −4 S cm −1 at room‐temperature and a lithium‐ion transference number of 0.64. More importantly, the DEPE exhibits outstanding interface compatibility with both the lithium anode and high‐voltage cathode. Benefiting from the weak adsorption of butadiene sulfone on lithium metal, a robust, LiF‐rich solid electrolyte interface is formed at the anode. In addition, its higher HOMO energy level facilitates the formation of a uniform, ‐SO x ‐rich cathode electrolyte interface on the high‐voltage cathode. As a result, a symmetrical Li||Li cell operates stably for over 1200 h, and full batteries of Li||NCM811 exhibit long‐term cycling stability even at 4.5 V. This study proposes an effective strategy for designing high‐performance PEs, paving the way for the development of high‐voltage, long‐life LMBs.
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