In Situ Orthogonal Polymerization for Constructing Fast-Charging and Long-Lifespan Li Metal Batteries with Topological Copolymer Electrolytes

被引:13
|
作者
Guo, Kairui [1 ]
Li, Shaoqiao [1 ]
Wang, Jirong [1 ]
Shi, Zhen [1 ]
Wang, Yong [1 ]
Xue, Zhigang [1 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Chem & Chem Engn, Key Lab Mat Chem Energy Convers & Storage, Hubei Key Lab Mat Chem & Serv Failure,Minist Educ, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
LITHIUM; OPPORTUNITIES; TRANSPORT; DESIGN;
D O I
10.1021/acsenergylett.3c02422
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Fast-charging Li metal batteries (LMBs) with low cost, high safety, and long lifespan are highly desirable for next-generation energy storage technologies yet have been rarely achieved. Here, we report the in situ fabrication of well-designed blend, block, and bottle-brush solid-state polymer electrolytes (SPEs) integrating poly(poly(ethylene glycol) methyl ether methacrylate) (PPEGMA) and poly(trimethylene carbonate) (PTMC) matrices via Li-catalyzed orthogonal polymerization. Among them, the bottle-brush topological SPEs may display quasi-molecular-scale miscibility between PPEGMA and PTMC, maximize the synergistic coordination of Li+ with ether and carbonate units at the PPEGMA/PTMC interface, and simultaneously exhibit ideal mass transport properties and a broad electrochemical stability window. Further incorporating trifluoroethyl methacrylate (TFEMA) into the bottle-brush SPE allows facile construction of a robust solid electrolyte interphase (SEI). These, together with the fast charge transfer kinetics inherited from the in situ polymerization technique, enable the development of the first example of solid-state polymeric LMB capable of operating steadily at 3C (73% capacity retention after 1000 cycles).
引用
收藏
页码:843 / 852
页数:10
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