聚合物电解质
电解质
电池(电)
固态
快离子导体
能量密度
聚合物
储能
材料科学
纳米技术
电化学
电化学窗口
有机自由基电池
电极
工程物理
工程类
复合材料
化学
离子电导率
功率(物理)
物理
物理化学
量子力学
作者
Mingyang Xin,Yanan Li,Lina Cong,Siru Chen,Xinming Zhang,Haiming Xie,Yulong Liu
出处
期刊:Acs Symposium Series
日期:2022-06-24
卷期号:: 135-165
被引量:1
标识
DOI:10.1021/bk-2022-1413.ch006
摘要
Polymer-based solid-state batteries exhibit desired properties of good safety and high energy density, and they are very likely to become the devices of choice for the next generation of energy storage. Among solid electrolytes, polyoxyethylene (PEO)-based polymer electrolytes are widely used in solid-state batteries. However, the electrochemical window of electrolytes themselves is narrow, which limits further improvement of energy density. At present, only LiFePO4 is suitable for paring with a PEO electrolyte, and such a limitation severely hinders the real-world application of PEO polymer solid-state batteries. In particular, the side reactions at the interface between the electrode material and the PEO polymer electrolyte are the main challenge that greatly shortens battery cycle life. To suppress these side reactions, people have adopted corresponding strategies and achieved considerable progress. In order to fully understand the changes at the interface of solid-state batteries, various advanced characterization methods have been employed. This will provide a more scientific basis for improving the cycle stability of solid-state batteries in the next stage.
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