离子键合
离子电导率
碱金属
反离子
电导率
离解(化学)
无机化学
电解质
共价键
离子
离子势
材料科学
化学
化学工程
物理化学
有机化学
电极
工程类
作者
Ye Gao,Wang‐Kang Han,Ruo‐Meng Zhu,Jiaxing Fu,Jingdong Feng,Zhi‐Guo Gu
出处
期刊:Small
[Wiley]
日期:2024-09-17
卷期号:20 (49): e2406251-e2406251
被引量:8
标识
DOI:10.1002/smll.202406251
摘要
Rational construction of high-performance ionic conductors is a critical challenge in the field of energy storage. In this study, a series of 1D anionic titanium-based covalent organic frameworks (COFs) containing abundant alkali metal ion migration sites, namely, COF-M-R (M = Li, Na, K; R = H, Me, Et), is constructed. The integration of negative TiO6 2- sites on 1D anionic COFs allows alkali metal cations to migrate directly through the channels. Meanwhile, the π-π stacking of 1D chain-to-chain allows the distribution of ion-migration sites in 2D planes. In view of this, multidimensional ionic transport in COFs is realized to achieve high ionic conductivity. COF-M-Rs exhibit an increased ionic conductivity as the counterions change from Li+ to Na+ to K+. Notably, COF-Na-Et has an impressive ionic conductivity as high as 0.81 × 10-3 S cm-1. The different decorated groups (H, Me, and Et) on the skeleton influence the dissociation of the cation from the polyanion. This study offers deep insights into the design of COF-based solid-state electrolytes to achieve high ionic conductivity by increasing the ionic transport dimensions.
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