Anion‐Modulated Solvated Structure for All‐Solid‐State Lithium Metal Batteries with Inorganic‐Rich SEI

IF 18.5 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Changyong Zhao, Yingkang Tian, Guozheng Sun, Yulong Liu, Xiaofei Yang, Runcang Sun, Xuejie Gao
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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 cm¹ 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.
具有富无机SEI的全固态锂金属电池的阴离子调制溶剂化结构
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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advanced Functional Materials
Advanced Functional Materials 工程技术-材料科学:综合
CiteScore
29.50
自引率
4.20%
发文量
2086
审稿时长
2.1 months
期刊介绍: Firmly established as a top-tier materials science journal, Advanced Functional Materials reports breakthrough research in all aspects of materials science, including nanotechnology, chemistry, physics, and biology every week. Advanced Functional Materials is known for its rapid and fair peer review, quality content, and high impact, making it the first choice of the international materials science community.
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