离子电导率
材料科学
锂(药物)
电解质
电极
电导率
聚合物
电化学
化学工程
准固态
化学
复合材料
色素敏化染料
物理化学
内分泌学
工程类
医学
作者
Wenyi Liu,Chengjun Yi,Linpo Li,Shuailei Liu,Qiuyue Gui,Deliang Ba,Yuanyuan Li,Dong‐Liang Peng,Jinping Liu
标识
DOI:10.1002/ange.202101537
摘要
Abstract Solid‐state lithium batteries (SSLBs) are promising owing to enhanced safety and high energy density but plagued by the relatively low ionic conductivity of solid‐state electrolytes and large electrolyte–electrode interfacial resistance. Herein, we design a poly(vinylidene fluoride‐co‐hexafluoropropylene) (PVDF‐HFP)‐based polymer‐in‐salt solid electrolyte (PISSE) with high room‐temperature ionic conductivity (1.24×10 −4 S cm −1 ) and construct a model integrated TiO 2 /Li SSLB with 3D fully infiltration of solid electrolyte. With forming aggregated ion clusters, unique ionic channels are generated in the PISSE, providing much faster Li + transport than common polymer electrolytes. The integrated device achieves maximized interfacial contact and electrochemical and mechanical stability, with performance close to liquid electrolyte. A pouch cell made of 2 SSLB units in series shows high voltage plateau (3.7 V) and volumetric energy density comparable to many commercial thin‐film batteries.
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