Facile fabrication of cross-linked polymer electrolyte via imidazole-based deep eutectic solvent-induced in situ polymerizations

被引:3
|
作者
Ye, Weixin [1 ]
Wang, Jirong [1 ,2 ]
Shi, Zhen [1 ]
Guo, Kairui [1 ]
Xue, Zhigang [1 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Chem & Chem Engn, Key Lab Mat Chem Energy Convers & Storage, Minist Educ,Hubei Key Lab Mat Chem & Serv Failure, Wuhan 430074, Peoples R China
[2] Qingdao Univ, Coll Text & Clothing, Inst Funct Text & Adv Mat, Natl Engn Res Ctr Adv Fire Safety Mat D&A Shandong, Qingdao 266071, Peoples R China
基金
中国国家自然科学基金;
关键词
Cross-linked polymer electrolytes; In situ polymerization; Ring-opening polymerization; Michael addition; Lithium-metal batteries; LITHIUM; NETWORK; RAMAN;
D O I
10.1016/j.memsci.2024.122541
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Fabricating the cross-linked network is an efficient strategy for improving the mechanical and electrochemical performances of polymer electrolytes (PEs). However, present methods used for the preparation of the cross-linked PEs is difficult to remove the residual catalyst and avoid the side reactions, and the ion conduction in solid PEs is often confined. Herein, we report that the deep eutectic solvent (DES) via the Li-N interaction of 1,2-dimethylimidazole (DMIm) and bis(trifluoromethane)sulfonimide lithium (LiTFSI) displays synergistic effects in inducing the ring-opening polymerization (ROP) of trimethylene carbonate (TMC) and thiol-Michael addition reaction, permitting in situ preparation of PEs with a cross-linked structure. Moreover, DMIm-based DES not only endows PEs with the flame-retardant property but also promotes the conduction of Li ions (Li+) in PEs, leading to a good ionic conductivity at 60 degrees C (1.8 x 10(-4) S cm(-1)) and Li+ transference number (0.41). Notably, no obvious short-circuit at 0.1 mA cm(-2) appears during the deposition process of lithium symmetric batteries assembled with PEs after 1200 h.
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收藏
页数:8
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