| Literature DB >> 33797171 |
Wenyi Liu1, Chengjun Yi1, Linpo Li2, Shuailei Liu1, Qiuyue Gui1, Deliang Ba2, Yuanyuan Li2, Dongliang Peng3, Jinping Liu1.
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 TiO2 /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.Entities:
Keywords: 3D electrolyte infiltration; interfacial engineering; nanostructured thin-film batteries; polymer-in-salt electrolytes; solid-state lithium batteries
Year: 2021 PMID: 33797171 DOI: 10.1002/anie.202101537
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336