聚丙烯腈
电解质
材料科学
化学工程
锂(药物)
锂硫电池
硫黄
膜
无机化学
聚合物
高分子化学
图层(电子)
纳米技术
有机化学
复合材料
化学
电极
物理化学
内分泌学
工程类
医学
生物化学
作者
Xiuli Wang,Xiaojing Hao,Yan Xia,Yanfei Liang,Xinhui Xia,J.P. Tu
标识
DOI:10.1016/j.memsci.2019.03.048
摘要
Owing to high theoretical capacity, lithium-sulfur batteries (LSBs) are receiving extensive researches. However, cyclic instability and safety issues hugely confine the commercial applications of traditional liquid LSBs. In this work, for the sake of fully leveraging the high ionic conductivity of polyacrylonitrile while avoiding Li anode “passivation effect” caused by CN group, we prepare double-layer gel polymer electrolytes for quasi-solid-state LSBs. The transition layer composed of polyacrylonitrile, polyethylene oxide and Li1.3Al0.3Ti1.7(PO4)3 (LATP) is located on Li anode side to reduce “passivation effect” triggered by pure polyacrylonitrile. Meanwhile, the high ionic conductivity layer composed of polyacrylonitrile and LATP in contact with cathode can utilize the high intrinsic ionic conductivity of polyacrylonitrile to enhance the rate performance. Furthermore, LATP with higher ionic conductivity embedded in the membrane serves as Li+ transport channels to further increase ionic conductivity. Prominently, the designed double-layer electrolytes exhibit a high Li+ transference number of 0.55 and superior mechanical property. Moreover, stable coulombic efficiency of 99.6–100.0% over 100 cycles and good capacity retention of 79.0% after 100 cycles at 0.1C can be achieved. Our newly designed double-layer electrolytes with multiple functions exhibit potential applications in safer LSBs.
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