Systematic synthesis of ZIF-67 derived Co3O4 and N-doped carbon composite for supercapacitors via successive oxidation and carbonization

被引:79
作者
Chen, Tzu-Yang [1 ]
Lin, Lu-Yin [1 ,2 ]
Geng, Dong-Sheng [3 ]
Lee, Pin-Yan [1 ]
机构
[1] Natl Taipei Univ Technol, Dept Chem Engn & Biotechnol, Taipei, Taiwan
[2] Res Ctr Energy Conservat New Generat Residential, Taipei, Taiwan
[3] Univ Sci & Technol Beijing, Ctr Green Innovat, Sch Math & Phys, Beijing 100083, Peoples R China
关键词
Carbonization; Cobalt oxide; N-doped carbon; Oxidation; Polyhedron; ZIF67;
D O I
10.1016/j.electacta.2021.137986
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Zeolitic imidazolate framework-67 (ZIF67) composed of cobalt metal and 2-methylimidazole is one of the attractive metal organic frameworks for energy storage, due to the possible formation of cobalt oxide and N-doped graphite via oxidation and carbonization processes. It is the first time to develop cobalt oxide and N-doped graphite in one ZIF67 derivative as active material for supercapacitor (SC), which stores charges via redox reactions and electric double-layered behaviors. Six active materials with careful designs are constructed, including carbonized ZIF67 (C67), oxidized C67 (C67/O), oxidized ZIF67-covered C67 (C67/O67), oxidized ZIF67 (O67), carbonized O67 (O67/C), and carbonized ZIF67-covered O67 (O67/C). Detailed formation process and mechanism of these active materials are provided. The highest areal capacitance (CA) of 332.3 mF/cm(2) at 20 mV/s is obtained for C67/O electrode, due to the suitable composition of Co3O4 and N-doped graphite as well as the particle-assembled polyhedron structure with high porosity. The asymmetric SC composed of C67/O electrodes shows a potential window of 1.0 V and the maximum energy density of 0.87 Wh/kg at power density of 150 W/kg. Excellent cycling stability with CA retention of 100% and Coulombic efficiency of 100% after 4000 times repeatedly charge/discharge process is also achieved for this asymmetric SC. (C) 2021 Elsevier Ltd. All rights reserved.
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页数:10
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