丁二腈
材料科学
电解质
离子电导率
锂(药物)
电化学
聚合物
快离子导体
离子键合
表面改性
化学工程
电导率
电化学窗口
离子
高分子化学
无机化学
电极
有机化学
化学
物理化学
复合材料
医学
工程类
内分泌学
作者
Xinyang Li,Zongnan Zhang,Jie Feng,Xiangkai Yin,Xiaofeng Cui,Wei Xu,Hongjun Zhang,Rong Zeng,Shujiang Ding
标识
DOI:10.1007/s40843-024-2857-8
摘要
Polyethylene oxide) (PEO) polymer electrolytes have the potential for the use in all-solid-state lithium-metal batteries (ASSLMBs). However, no effective rules have been proposed to prepare all-solid-state PEO electrolytes that overcome the limitation being unusable at room temperature. In this study, based on the polymer C–H functionalization strategy, we design a highly ion-conductive PEO electrolyte by directly covalently linking succinonitrile functional-groups with lithium coordination activity on the polymer chains. The functional-groups enhance the disorder and mobility of the PEO chains while acting as effective sites for the fast ionic-conduction in the interchain, thus achieving a dual optimization of the free volume around ions and the migration behavior. Due to the precise tuning by functional-groups, the functionalized electrolyte exhibits enhanced ionic conductivity (>102 times), high transference number (~0.51) and wide electrochemical window (~0.47 V). In particular, the functionalized PEO300k electrolyte with a high ionic conductivity (1.01×10−4 S cm−1 at 25°C) enables the stable operation at room temperature, providing a path for the development of polymer-based electrolytes with practical applications.
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