材料科学
弹性体
电解质
锂(药物)
相间
离子电导率
电极
电导率
储能
化学工程
金属
金属锂
磁滞
纳米技术
离子键合
合金
复合材料
曲折
溶解
纳米孔
导电体
快离子导体
共价键
能量密度
极限抗拉强度
作者
Wenya Lei,Baoyu Sun,Jiangning Liu,Caiwang Mao,Tuo Zhao,Chen Shengjie,Mahalingam Ravivarma,Chaofan Zhang,Deng Junkai,Hao Fan,Jiangxuan Song
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-12-30
卷期号:26 (1): 18-26
标识
DOI:10.1021/acs.nanolett.5c00968
摘要
All-solid-state lithium metal batteries offer high energy density and enhanced safety, yet stable cycling remains difficult due to the incompatibility among inorganic phases such as solid electrolyte particles and lithium metal. Here, we address this issue by chemical grafting inorganic components with a dynamic elastomer, achieving an ultrastrong-tough maximum tensile strain of 925%. This strategy replaces weak physical contacts between inorganic phases with Si-O-Li covalent linkages to strengthen structural integrity, while dynamic hydrogen-bond reconstruction ensures high interfacial compatibility. Benefiting from this mechanism, Li+ transfer tortuosity is reduced and the ionic conductivity reaches 4.0 × 10-3 S cm-1. As a result, symmetric cells exhibit stable cycles that exceed 3000 h at 1.0 mA cm-2. Further, the full cell and fabricated pouch cell exhibit wide temperature adaptability (-40 to 80 °C) and high plasticity, respectively. This research provides a general solution for all-solid-state batteries to address the incompatibility among inorganic phases.
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