电解质
锂(药物)
材料科学
环氧乙烷
氧化物
化学工程
阴极
锂电池
锂钴氧化物
聚合物
锂离子电池
电化学
电池(电)
无机化学
化学
离子
电极
离子键合
共聚物
有机化学
复合材料
冶金
功率(物理)
物理化学
内分泌学
工程类
物理
医学
量子力学
作者
Jun Ma,Zhaolin Liu,Bingbing Chen,Longlong Wang,Liping Yue,Haisheng Liu,Jianjun Zhang,Zhihong Liu,Guanglei Cui
摘要
Interface stability between cathode and electrolyte is closely related to the interface resistance and electrochemical performance of all-solid-state lithium ion batteries (LIBs). However, the significant interface issues between cathode and all-solid-state polymer electrolyte have been researched rarely. Here, we demonstrate that severe interface decomposition reactions occur continually and deteriorate the cycling life of high voltage LiCoO2/cellulose-supported poly(ethylene oxide) (PEO)-lithium difluoro(oxalato)borate (LiDFOB)/Li battery between 2.5 and 4.45 V vs. Li/Li+. To improve the interface stability between LiCoO2 and PEO-LiDFOB electrolyte, we modify the LiCoO2 surface by a thin layer of high ionic conducting and electrochemical oxidation resistant poly(ethyl cyanoacrylate) (PECA) through in-situ polymerization method. The PECA coating layer significantly suppresses the continuous decomposition of lithium difluoro(oxalato)borate (LiDFOB) salt in PEO electrolyte. As a result, the PECA-coated LiCoO2/PEO-LiDFOB/Li battery shows decreased interface resistance and enhanced cycling stability. This work will enlighten the understanding of interface stability and enrich the modification strategy between cathode and polymer electrolyte as well as boost the further development of all-solid-state LIBs.
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