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
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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