电解质
离子电导率
溶剂化
阳极
离子键合
电化学
材料科学
聚合物电解质
聚合物
电导率
化学工程
共价键
相容性(地球化学)
硅
增塑剂
无机化学
纳米技术
快离子导体
离子液体
有机自由基电池
电极
电化学电池
高分子化学
电化学窗口
化学
作者
Tao Cai,Fei Zhao,Pushpendra Kumar,Hao Yu,Zexu Wang,Akang Huang,Wandi Wahyudi,Qian Li,Tianming Feng,Yingjun Guo,Zheng Ma,Jun Ming
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-11-25
标识
DOI:10.1021/acs.nanolett.5c04737
摘要
The practical application of solid polymer electrolytes (SPEs) is limited by their low ionic conductivity and poor interfacial compatibility with silicon (Si) anodes in high-energy-density, safe lithium-ion batteries (LIBs). Here, we introduce a lithiated covalent organic framework (COF) into a poly(vinylidene fluoride-cohexafluoropropylene) (PVDF-HFP)-based quasi-solid polymer electrolyte (QSPE) containing plasticizers to increase its electrochemical performance. The resulting COF-based QSPE has a high ionic conductivity of 2.99 mS cm-1 and enables Si anodes to deliver a remarkable specific capacity of 1722 mAh g-1 after 500 cycles, along with an excellent rate capability of up to 10 A g-1. Furthermore, we provide new insights into the role of lithiated COFs in modulating the Li+ solvation structure, facilitating ionic migration and promoting desolvation in plasticizer-containing solid electrolytes at the molecular scale. These findings offer valuable guidelines for the rational design of stable Si anodes in solid-state batteries.
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