Molecular Self-Assembled Ether-Based Polyrotaxane Solid Electrolyte for Lithium Metal Batteries

被引:79
作者
Ding, Peipei [1 ,2 ]
Wu, Lingqiao [1 ,2 ]
Lin, Zhiyuan [1 ,2 ]
Lou, Chenjie [3 ]
Tang, Mingxue [3 ]
Guo, Xianwei [1 ,2 ]
Guo, Hongxia [1 ,2 ]
Wang, Yongtao [1 ,2 ]
Yu, Haijun [1 ,2 ]
机构
[1] Beijing Univ Technol, Inst Adv Battery Mat & Devices, Fac Mat & Mfg, Beijing 100124, Peoples R China
[2] Beijing Univ Technol, Key Lab Adv Funct Mat, Minist Educ, Beijing 100124, Peoples R China
[3] Ctr High Pressure Sci & Technol Adv Res, Beijing 100094, Peoples R China
基金
中国博士后科学基金; 北京市自然科学基金; 国家重点研发计划; 中国国家自然科学基金;
关键词
POLYMER ELECTROLYTE; ION-TRANSPORT; NETWORK; CONDUCTIVITY; GLYCOL); ANODE; NMR;
D O I
10.1021/jacs.2c06512
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Poly(ethylene oxide) has been widely investigated as a potential separator for solid-state lithium metal batteries. However, its applications were significantly restricted by low ionic conductivity and a narrow electrochemical stability window (<4.0 V vs Li/Li+) at room temperature. Herein, a novel molecular self-assembled ether-based polyrotaxane electrolyte was designed using different functional units and prepared by threading cyclic 18-crown ether-6 (18C6) to linear poly(ethylene glycol) (PEG) via intermolecular hydrogen bond and terminating with hexamethylene diisocyanate trimer (HDIt), which was strongly confirmed by local structure-sensitive solid/liquid-state nuclear magnetic resonance (NMR) techniques. The designed electrolyte has shown an obviously increased room-temperature ionic conductivity of 3.48 x 10-4 S cm-1 compared to 1.12 x 10-5 S cm-1 without assembling polyrotaxane functional units, contributing to the enhanced cycling stability of batteries with both LiFePO4 and LiNi0.8Co0.15Al0.05O2 cathode materials. This advanced molecular self-assembled strategy provides a new paradigm in designing solid polymer electrolytes with demanded performance for lithium metal batteries.
引用
收藏
页码:1548 / 1556
页数:9
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