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具有高电化学电容器性能的钼基晶体多金属有机框架材料。

Mo-Based crystal POMOFs with a high electrochemical capacitor performance.

作者信息

Chai Dongfeng, Xin Jianjiao, Li Bonan, Pang Haijun, Ma Huiyuan, Li Kunqi, Xiao Boxin, Wang Xinming, Tan Lichao

机构信息

School of Materials Science and Engineering, College of Chemical and Environmental Engineering, Harbin University of Science and Technology, Harbin 150040, P. R. China.

出版信息

Dalton Trans. 2019 Sep 14;48(34):13026-13033. doi: 10.1039/c9dt02420d. Epub 2019 Aug 12.

DOI:10.1039/c9dt02420d
PMID:31403634
Abstract

Mo-Based crystalline polyoxometalate-based metal-organic frameworks (POMOFs), namely, [CuH(CHN)(PMoO)]·[(CHN)(HO)] (1) and [Cu(CHN)(PMoMoO)] (2) (CHN, 1,4-bis(triazol-1-ylmethyl) benzene, abbreviation btx) as promising capacitor electrode materials were synthesized by a hydrothermal reaction. Compound 1 consisted of two-dimensional (2D) lattice structures with free triethylamine (abbreviation, TEA) molecules and HO molecules, and compound 2 showed a 3D host-guest structure, in which 1D polyoxometalate (POM) chains were encapsulated into a 3D Cu(ii)-btx metal-organic framework (MOF). The compound 1-based electrode showed much higher specific capacitance (249.0 F g at 3 A g) than the 2-based one (154.5 F g at 3 A g). Moreover, the specific capacitance of the 1-based electrode was not only higher than those of the majority of the reported POMOF materials as supercapacitors, but also higher than those of most state-of-the-art MOF-based and POM-based supercapacitor electrode materials. This superior capacitance performance of the 1-based electrode could be attributed to the high redox capacity and excellent electronic conductivity. More importantly, this work may open a new avenue for optimizing the performance of POMOF-based capacitor electrode materials.

摘要

基于钼的晶态多金属氧酸盐基金属有机框架材料(POMOFs),即[CuH(CHN)(PMoO)]·[(CHN)(HO)](1)和[Cu(CHN)(PMoMoO)](2)(CHN为1,4 - 双(三唑 - 1 - 基甲基)苯,缩写为btx)作为有前景的电容器电极材料,通过水热反应合成。化合物1由具有游离三乙胺(缩写为TEA)分子和HO分子的二维(2D)晶格结构组成,化合物2呈现三维主客体结构,其中一维多金属氧酸盐(POM)链被封装在三维Cu(II)-btx金属有机框架(MOF)中。基于化合物1的电极在3 A g下显示出比基于化合物2的电极(在3 A g下为154.5 F g)高得多的比电容(249.0 F g)。此外,基于化合物1的电极的比电容不仅高于大多数已报道的作为超级电容器的POMOF材料,而且高于大多数最先进的基于MOF和基于POM的超级电容器电极材料。基于化合物1的电极的这种优异电容性能可归因于高氧化还原容量和优异的电子导电性。更重要的是,这项工作可能为优化基于POMOF的电容器电极材料的性能开辟一条新途径。

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