溶剂
共价键
材料科学
共价有机骨架
锂(药物)
金属
分离器(采油)
氢键
分子
化学工程
化学
无机化学
电解质
电极
有机化学
物理化学
热力学
工程类
物理
内分泌学
医学
作者
Yan Yang,Shi‐Yan Yao,Ziwei Liang,Yucheng Wen,Jun Liu,Yiwen Wu,Jun Liu,Min Zhu
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2022-02-02
卷期号:7 (2): 885-896
被引量:100
标识
DOI:10.1021/acsenergylett.1c02719
摘要
Covalent organic frameworks (COF) displayed strong affinity between COF and Li+ in terms of previous works. However, the relationship of COF and solvent molecules in the electrolyte was exclusive. Herein, a self-supporting COF separator (TPB-BD(OH)2-COF) was synthesized and served as a separator in lithium metal batteries. The formation of hydrogen bond network is due to the interaction of hydroxyl functional group (−OH) in TPB-BD(OH)2-COF and −OH···F and −OH···O in PF6–, EC and EMC within solvent sheath to achieve the desolvation process and realize more aggregative electrolyte, thus reducing the free solvent and lithium metal side effects. Therefore, the full cell assembled with self-supporting COF displayed superior cycling stability with a reversible capacity of 114.3 mAh g–1 after 335 cycles at a current density of 1C and a capacity of 5 mAh cm–2. Moreover, the COF separator can perform well even in extreme environments (temperature 60 °C).
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