聚丙烯腈
电解质
阳极
材料科学
离子电导率
锂(药物)
聚合物
电池(电)
阴极
锂电池
化学工程
电导率
金属锂
无机化学
盐(化学)
离子键合
电极
离子
化学
复合材料
有机化学
功率(物理)
物理化学
内分泌学
工程类
物理
医学
量子力学
作者
Hongcai Gao,Nicholas S. Grundish,Yongjie Zhao,Aijun Zhou,John B. Goodenough
标识
DOI:10.34133/2021/1932952
摘要
The integration of solid-polymer electrolytes into all-solid-state lithium batteries is highly desirable to overcome the limitations of current battery configurations that have a low energy density and severe safety concerns. Polyacrylonitrile is an appealing matrix for solid-polymer electrolytes; however, the practical utilization of such polymer electrolytes in all-solid-state cells is impeded by inferior ionic conductivity and instability against a lithium-metal anode. In this work, we show that a polymer-in-salt electrolyte based on polyacrylonitrile with a lithium salt as the major component exhibits a wide electrochemically stable window, a high ionic conductivity, and an increased lithium-ion transference number. The growth of dendrites from the lithium-metal anode was suppressed effectively by the polymer-in-salt electrolyte to increase the safety features of the batteries. In addition, we found that a stable interphase was formed between the lithium-metal anode and the polymer-in-salt electrolyte to restrain the uncontrolled parasitic reactions, and we demonstrated an all-solid-state battery configuration with a LiFePO 4 cathode and the polymer-in-salt electrolyte, which exhibited a superior cycling stability and rate capability.
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