电解质
材料科学
快离子导体
电导率
陶瓷
共价键
共价有机骨架
化学工程
导电体
离子电导率
膜
耐久性
纳米技术
电极
复合材料
有机化学
化学
工程类
生物化学
物理化学
多孔性
作者
Dong Guo,Digambar Balaji Shinde,Woochul Shin,Edy Abou‐Hamad,Abdul‐Hamid Emwas,Zhiping Lai,Arumugam Manthiram
标识
DOI:10.1002/adma.202201410
摘要
Abstract Solid‐state electrolytes with high Li + conductivity, flexibility, durability, and stability offer an attractive solution to enhance safety and energy density. However, meeting these stringent requirements poses challenges to the existing solid polymeric or ceramic electrolytes. Here, an electrolyte‐mediated single‐Li + ‐conductive covalent organic framework (COF) is presented, which represents a new category of quality solid‐state Li + conductors. In situ solidification of a tailored liquid electrolyte boosts the charge‐carrier concentration in the COF channels, decouples Li + cations from both COF walls and molecular chains, and eliminates defects by crystal soldering. Such an altered microenvironment activates the motion of Li + ions in a directional manner, which leads to an increase in Li + conductivity by 100 times with a transference number of 0.85 achieved at room temperature. Moreover, the electrolyte conversion cements the ultrathin COF membrane with fortified mechanical toughness. With the COF membrane, foldable solid‐state pouch cells are demonstrated.
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