{"title":"Anion‐Modulated Solvated Structure for All‐Solid‐State Lithium Metal Batteries with Inorganic‐Rich SEI","authors":"Changyong Zhao, Yingkang Tian, Guozheng Sun, Yulong Liu, Xiaofei Yang, Runcang Sun, Xuejie Gao","doi":"10.1002/adfm.202512870","DOIUrl":null,"url":null,"abstract":"The limited salt dissociation efficiency and unstable (Li(DMF)x)<jats:sup>+</jats:sup> 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<jats:sup>−1</jats:sup>) 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<jats:sup>−</jats:sup>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<jats:sup>+</jats:sup> transport and interfacial stability, paving the way for high‐performance solid‐state batteries.","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"21 1","pages":""},"PeriodicalIF":18.5000,"publicationDate":"2025-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adfm.202512870","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
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.
在聚偏氟乙烯(PVDF)基固态电解质(sse)中,有限的盐解离效率和不稳定的(Li(DMF)x)+溶剂化结构显著阻碍了高速率离子传输和电极-电解质界面稳定性。然而,开发结合高离子电导率(>1 mS cm−1)和稳定电极-电解质界面的sse仍然是一个重大的科学挑战。本文提出了一种采用PVDF - SCS(经苯磺酸化壳聚糖修饰的PVDF)电解质的高压固态锂金属电池。磺胺壳聚糖(SCS)中的氮基阴离子受体通过优先的阴离子对破坏促进了锂盐的解离,从而提高了游离Li⁺的浓度。关键是,缺电子氮中心表现出与锂盐阴离子的强配位,促进了它们的电化学还原,形成了稳定的阴离子衍生的固体电解质界面(SEI)。因此,PVDF‐SCS电解质显示出Li +的电导率提高到1.35 mS cm−1,并有效地减缓了枝晶生长,使Li|PVDF‐SCS|NCM523电池在4.3 V高压下稳定运行400次。这项工作证明了阴离子工程可以同时增强Li+的传输和界面稳定性,为高性能固态电池铺平了道路。
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