电解质
材料科学
锂(药物)
电导率
电化学
快离子导体
聚合
聚合物
化学工程
锂电池
离子键合
复合材料
化学
离子
电极
离子电导率
有机化学
工程类
物理化学
内分泌学
医学
作者
Qing Zhao,Xiaotun Liu,Sanjuna Stalin,Kasim Khan,Lynden A. Archer
出处
期刊:Nature Energy
[Nature Portfolio]
日期:2019-03-11
卷期号:4 (5): 365-373
被引量:869
标识
DOI:10.1038/s41560-019-0349-7
摘要
Solid-state electrolytes with high room-temperature ionic conductivity and fast interfacial charge transport are a requirement for practical solid-state batteries. Here, we report that cationic aluminium species initiate ring-opening polymerization of molecular ethers inside an electrochemical cell to produce solid-state polymer electrolytes (SPEs), which retain conformal interfacial contact with all cell components. SPEs exhibit high ionic conductivity at room temperature (>1 mS cm−1), low interfacial resistances, uniform lithium deposition and high Li plating/striping efficiencies (>98% after 300 charge–discharge cycles). Applications of SPEs in Li–S, Li–LiFePO4 and Li–LiNi0.6Mn0.2Co0.2O2 batteries further demonstrate that high Coulombic efficiency (>99%) and long life (>700 cycles) can be achieved with an in situ SPE design. Our study therefore provides a promising direction for creating solid electrolytes that meet both the bulk and interfacial conductivity requirements for practical solid polymer batteries. High-performance polymer electrolytes are highly sought after in the development of solid-state batteries. Lynden Archer and co-workers report an in situ polymerization of liquid electrolytes in a lithium battery for creating promising polymer electrolytes with high ionic conductivity and low interfacial resistance.
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