Enhancing mechanical properties of composite solid electrolyte by ultra-high molecular weight polymers

被引:1
|
作者
Deng, Hongjie [1 ]
He, Fa [1 ]
Liu, Tongli [1 ]
Ye, Meng [1 ]
Wan, Fang [1 ]
Guo, Xiaodong [1 ]
机构
[1] Sichuan Univ, Sch Chem Engn, Chengdu 610065, Peoples R China
基金
中国国家自然科学基金;
关键词
lithium battery; composite solid electrolytes; polymer in ceramic; poly(vinylidene fluoride); flexible films; LITHIUM; MEMBRANES; ANODES;
D O I
10.1088/1361-6528/ad27ad
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Composite solid electrolytes combining the advantages of inorganic and polymer electrolytes are considered as one of the promising candidates for solid-state lithium metal batteries. Compared with ceramic-in-polymer electrolyte, polymer-in-ceramic electrolyte displays excellent mechanical strength to inhibit lithium dendrite. However, polymer-in-ceramic electrolyte faces the challenges of lack of flexibility and severely blocked Li+ transport. In this study, we prepared polymer-in-ceramic film utilizing ultra-high molecular weight polymers and ceramic particles to combine flexibility and mechanical strength. Meanwhile, the ionic conductivity of polymer-in-ceramic electrolytes was improved by adding excess lithium salt in polymer matrix to form polymer-in-salt structure. The obtained film shows high stiffness (10.5 MPa), acceptable ionic conductivity (0.18 mS cm-1) and high flexibility. As a result, the corresponding lithium symmetric cell stably cycles over 800 h and the corresponding LiFePO4 cell provides a discharge capacity of 147.7 mAh g-1 at 0.1 C without obvious capacity decay after 145 cycles.
引用
收藏
页数:8
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