材料科学
锂(药物)
金属锂
固态
离子
无机化学
金属
纳米技术
工程物理
物理化学
冶金
电解质
电极
有机化学
化学
医学
工程类
内分泌学
作者
Changyong Zhao,Yingkang Tian,Guo-Zheng Sun,Yulong Liu,Xiaofei Yang,Run‐Cang Sun,Xuejie Gao
标识
DOI:10.1002/adfm.202512870
摘要
Abstract The limited salt dissociation efficiency and unstable (Li(DMF)x) + solvation structures in poly(vinylidene fluoride) (PVDF)‐based solid‐state electrolytes (SSEs) significantly impede both high‐rate ion transport and electrode‐electrolyte interfacial stability. However, developing SSEs that combine high ionic conductivity (>1 mS cm −1 ) with stable electrode‐electrolyte interfaces remains a major scientific challenge. Here, a high‐voltage solid‐state lithium‐metal battery is presented employing a PVDF‐SCS (PVDF modified with benzenesulfonylated chitosan) electrolyte. The nitrogen‐based anionic receptors in sulfonamide chitosan (SCS) facilitated lithium salt dissociation through preferential anion‐cation pair disruption, thereby enhancing the free Li⁺ concentration. Crucially, the electron‐deficient nitrogen centers exhibit strong coordination with lithium salt anions, promoting their electrochemical reduction and forming a stable, anion‐derived solid electrolyte interphase (SEI). Consequently, the PVDF‐SCS electrolyte demonstrates an elevated Li⁺ conductivity of 1.35 mS cm − ¹ and effectively mitigates dendritic growth, enabling a stable operation of Li|PVDF‐SCS|NCM523 full batteries for 400 cycles at a high voltage of 4.3 V. This work demonstrates the anion engineering can simultaneously enhance Li + transport and interfacial stability, paving the way for high‐performance solid‐state batteries.
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