电解质
材料科学
电化学
快离子导体
离子电导率
锂(药物)
化学工程
电极
储能
金属锂
电导率
锂离子电池的纳米结构
金属
离子键合
离子
无机化学
化学
有机化学
物理化学
冶金
热力学
内分泌学
工程类
功率(物理)
医学
物理
作者
Zhendi Wu,Yikun Yi,Feng Hai,Xiaolu Tian,Shentuo Zheng,Jingyu Guo,Wei Tang,Weibo Hua,Mingtao Li
标识
DOI:10.1021/acsami.3c00988
摘要
Solid-state lithium metal batteries are promising next-generation rechargeable energy storage systems. However, the poor compatibility of the electrode/electrolyte interface and the low lithium ion conductivity of solid-state electrolytes are key issues hindering the practicality of solid-state electrolytes. Herein, rational designed metal–organic frameworks (MOFs) with the incorporation of two types of ionic liquids (ILs) are fabricated as quasi-solid electrolytes. The obtained MOF-IL electrolytes offer continuous ion transport channels with the functional sulfonic acid groups serving as lithium ion hopping sites, which accelerate the Li+ transport both in the bulk and at the interfaces. The quasi-solid MOF-IL electrolytes exhibit competitive ionic conductivities of over 3.0 × 10–4 S cm–1 at room temperature, wide electrochemical windows over 5.2 V, and good interfacial compatibility, together with greatly enhanced Li+ transference numbers compared to the bare IL electrolyte. Consequently, the assembled quasi-solid Li metal batteries show either superior stability at low C rates or improved rate performance, related to the species of ILs. Overall, the quasi-solid MOF-IL electrolytes possess great application potential in high-safety and high-energy-density lithium metal batteries.
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