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Designing Polymer‐in‐Salt Electrolyte and Fully Infiltrated 3D Electrode for Integrated Solid‐State Lithium Batteries
Author(s) -
Liu Wenyi,
Yi Chengjun,
Li Linpo,
Liu Shuailei,
Gui Qiuyue,
Ba Deliang,
Li Yuanyuan,
Peng Dongliang,
Liu Jinping
Publication year - 2021
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.202101537
Subject(s) - electrolyte , ionic conductivity , materials science , electrochemistry , electrode , chemical engineering , polymer , conductivity , lithium (medication) , quasi solid , composite material , chemistry , dye sensitized solar cell , medicine , engineering , endocrinology
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.