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共价有机框架中受限的聚乙二醇提供的快速离子传输途径

Fast Ion Transport Pathway Provided by Polyethylene Glycol Confined in Covalent Organic Frameworks.

作者信息

Guo Zhenbin, Zhang Yuanyuan, Dong Yu, Li Jie, Li Siwu, Shao Pengpeng, Feng Xiao, Wang Bo

机构信息

Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, Key Laboratory of Cluster Science, Ministry of Education, School of Chemistry and Chemical Engineering , Beijing Institute of Technology , Beijing 100081 , People's Republic of China.

出版信息

J Am Chem Soc. 2019 Feb 6;141(5):1923-1927. doi: 10.1021/jacs.8b13551. Epub 2019 Jan 24.

Abstract

Covalent organic frameworks (COFs) with well-tailored channels are able to accommodate ions and offer their conduction pathway. However, due to strong Coulombic interaction and the lack of transport medium, directly including lithium salts into the channels of COFs results in limited ion transport capability. Herein, we propose a strategy of incorporating low-molecular-weight polyethylene glycol (PEG) into COFs with anionic, neutral, or cationic skeletons to accelerate Li conduction. The PEG confined in the well-aligned channels retains high flexibility and Li solvating ability. The ion conductivity of PEG included in a cationic COF can reach 1.78 × 10 S cm at 120 °C. The simplicity of this strategy as well as the diversity of crystalline porous materials holds great promise to design high-performance all-solid-state ion conductors.

摘要

具有精心定制通道的共价有机框架(COFs)能够容纳离子并提供其传导途径。然而,由于强烈的库仑相互作用以及缺乏传输介质,直接将锂盐纳入COFs的通道会导致离子传输能力有限。在此,我们提出一种将低分子量聚乙二醇(PEG)纳入具有阴离子、中性或阳离子骨架的COFs中以加速锂传导的策略。限制在排列良好的通道中的PEG保留了高柔韧性和锂溶剂化能力。包含在阳离子COF中的PEG在120°C时的离子电导率可达1.78×10 S cm。该策略的简单性以及结晶多孔材料的多样性为设计高性能全固态离子导体带来了巨大希望。

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