In-situ plasticized polymer electrolyte with double-network for flexible solid-state lithium-metal batteries

被引:236
作者
Duan, Hui [1 ,2 ]
Yin, Ya-Xia [1 ,2 ]
Zeng, Xian-Xiang [1 ,2 ]
Li, Jin-Yi [1 ,2 ]
Shi, Ji-Lei [1 ,2 ]
Shi, Yang [1 ,2 ]
Wen, Rui [1 ]
Guo, Yu-Guo [1 ,2 ]
Wan, Li-Jun [1 ,2 ]
机构
[1] Chinese Acad Sci, CAS Key Lab Mol Nanostruct & Nanotechnol, CAS Res Educ Ctr Excellence Mol Sci, Inst Chem, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Electrochemical energy storages; Batteries; Solid electrolytes; Flexible batteries; Nanostructures; IONIC-CONDUCTIVITY ENHANCEMENT; POLY(ETHYLENE OXIDE); SODIUM BATTERIES; TEMPERATURE; MEMBRANES; ANODE; SUCCINONITRILE; NANOCOMPOSITES; PERFORMANCE; COPOLYMERS;
D O I
10.1016/j.ensm.2017.06.017
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
Flexible solid polymer electrolyte (SPE) confers lithium-based batteries with high energy densities and diverse packaging. However, the application of SPE is hindered by the contradiction between ionic conductivity and mechanical strength. Herein, this issue can be effectively addressed by constructing an in-situ plasticized SPE with double-network (DN-SPE) through reasonably controlling the chain length of constitutional unit. With the self-plasticization of its double network, the bendable DN-SPE exhibits increased ionic conductivity (from 10(-5) to 10(-4.)5 S cm(-1) at room temperature), high thermal stability (up to 200 degrees C) and good capacity to suppress the growth of lithium dendrite. The resultant solid-state lithium-metal batteries exhibit admirable reversible specific capacity. Notably, pouch cells maintain their electrochemical functions well even under stringent bending and truncated conditions. Structural modulation of the in-situ plasticized DN-SPE demonstrates an effective strategy to enhance the ion conductivity of SPE and might grasp new insights into flexible solid-state lithium- metal batteries.
引用
收藏
页码:85 / 91
页数:7
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