电解质
材料科学
离子电导率
聚合物
阳极
化学工程
电化学
电化学窗口
电导率
阴极
快离子导体
锂(药物)
电极
复合材料
化学
内分泌学
工程类
物理化学
医学
作者
Haoyu Wu,Shuofeng Jian,Shida Xue,Ziting Ma,Changgang Li,Shuolei Deng,Wenhao Feng,Yaowen Cao,Qianqian Dou,Luyi Yang,Yifan Dong
标识
DOI:10.1016/j.jpowsour.2023.233613
摘要
Solid polymer electrolytes suffer from relatively low Li+ conductivity, poor mechanical strength and interfacial incompatibility with electrodes, which hinder their further application in solid-state batteries. In this work, one-dimension (1D) wollastonite fillers are introduced into the solid polymer electrolyte, which not only contribute to the improved mechanical strength and electrochemical window, but also effectively inhibit polymer crystallization. More importantly, the abundant Lewis sites at wollastonite surface provide 1D ion pathway to boost ion transport in the electrolyte, achieving high ionic conductivity and Li+ transfer number. Owing to these favorable properties, the as-prepared polymer electrolyte exhibits enhanced interfacial stability toward Li anode, enabling long-term cycling in a Li-Li symmetric cell without short circuit. Showing good interfacial compatibility with both LiFePO4 and LiCoO2 cathode materials, the modified polymer electrolyte delivers high rate capability (143 mAh g−1 at 5C) and stable cycling performance (capacity retention of 93.12% after 380 cycles) in full cells. Through regulating the interfacial interactions between polymer matrix and fillers, this work points out a new direction towards high-performance all-solid-state batteries.
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