电解质
材料科学
电化学窗口
分离器(采油)
电化学
化学工程
复合数
原位聚合
阴极
聚合
电极
离子电导率
复合材料
聚合物
化学
物理
工程类
物理化学
热力学
作者
Bowei Cao,Yuli Huang,Wenzhuo Cao,Kun Zhou,Zhen Geng,Hong Li
标识
DOI:10.1021/acsaem.3c01667
摘要
The poor interfacial contact between solid-state electrolytes (SSEs) and electrodes, which hinders the applications of solid-state batteries (SSBs), could be improved by in situ polymerization. However, the limited electrochemical window and insufficient mechanical strength of in situ-polymerized electrolytes make them unable to match high-voltage cathodes and inhibit lithium dendrites. Here, a layered organic–inorganic composite solid-state electrolyte structure is designed by introducing a Li1.3Al0.3Ti1.7(PO4)3 (LATP)-coated polyethylene separator and fluoroethylene carbonate (FEC) into in situ-polymerized 1,3-dioxolane (DOL). The high-voltage stable fluoride-rich cathode–electrolyte interface formed in situ by FEC widens the electrochemical window of the composite solid-state electrolyte. In addition, the LATP coating layer inhibits the growth of lithium dendrites and increases the Li-ion conductivity by reacting with FEC to generate FEC derivatives. The Li/LiCoO2 battery exhibits good cycling and rate performance with a cutoff voltage of 4.3 V at room temperature. It provides a simple and practical solution to improve the performance of high-voltage lithium metal batteries based on in situ polymerization.
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