Negative electrodes for supercapacitors with good performance using conductive bismuth-catecholate metal-organic frameworks

被引:3
|
作者
Chen, Si [1 ]
Zhang, Haoliang [1 ]
Li, Xu [1 ]
Liu, Yong [1 ]
Zhang, Mingyi [2 ]
Gao, Xiangyang [1 ]
Chang, Xin [2 ]
Pu, Xiangjun [3 ]
He, Chunqing [1 ]
机构
[1] Wuhan Univ, Sch Phys & Technol, Key Lab Nucl Solid State Phys Hubei Prov, Wuhan 430072, Peoples R China
[2] Harbin Normal Univ, Sch Phys & Elect Engn, Key Lab Photon & Elect Bandgap Mat, Minist Educ, Harbin 150025, Peoples R China
[3] Wuhan Univ, Coll Chem & Mol Sci, Key Lab Electrochem Power Sources, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
NANOSHEETS; CARBON; NANOPARTICLES;
D O I
10.1039/d3dt00117b
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Metal-organic frameworks (MOFs) have attracted increasing research interest in various fields. Unfortunately, the poor conductivity of most traditional MOFs considerably hinders their application in energy storage. Benefiting from the full charge delocalization in the atomic plane, two-dimensional conductive coordination frameworks achieve good electrochemical performance. In this work, pi-pi coupling conductive bismuth-catecholate nanobelts with tunable lengths, Bi(HHTP) (HHTP = 2,3,6,7,10,11-hexahydroxytriphenylene), are synthesized by a simple hydrothermal reaction and their length-dependent electrochemical properties are also investigated. The Bi(HHTP) nanobelts (about 10 mu m in length) possess appropriate porosity, numerous redox active sites and good electrical conductivity. Being a negative electrode for supercapacitors, Bi(HHTP) nanobelts display a high specific capacitance of 234.0 F g(-1) and good cycling stability of 72% after 1000 cycles. Furthermore, the mechanism of charge storage is interpreted for both battery-type and surface-capacitive behavior. It is believed that the results of this work will help to develop battery-type negative electrode materials with promising electrochemical performance using some newly designed pi-pi coupling conductive coordination frameworks.
引用
收藏
页码:4826 / 4834
页数:9
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