Anchoring Ni-MOF nanosheet on carbon cloth by zeolite imidazole framework derived ribbonlike Co3O4 as integrated composite cathodes for advanced hybrid supercapacitors

被引:18
作者
Zhang, Feng [1 ]
Zhang, Junli [1 ]
Song, Jun [2 ]
You, Yan [1 ]
Jin, Xueli [1 ]
Ma, Jinjin [1 ]
机构
[1] Huanghuai Univ, Sch Chem & Pharmaceut Engn, Zhumadian 463000, Peoples R China
[2] Huanghuai Univ, Sch Mech & Energy Engn, Zhumadian 463000, Peoples R China
关键词
Metal-organic frameworks; Nanosheet; Zeolite imidazole framework; Supercapacitor; HIGH-PERFORMANCE ELECTRODE; METAL-ORGANIC FRAMEWORKS; BINDER-FREE ELECTRODE; FACILE SYNTHESIS; ARRAYS; ENERGY;
D O I
10.1016/j.ceramint.2021.01.269
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Metal-organic frameworks (MOFs) and their derivatives as electrode materials for energy storage and conversion are intriguing. However, the in-situ uniformly and firmly growing metal-organic framework materials directly on conductive substrates is limited and still challenging. Herein, an effective strategy is presented by constructing a ribbonlike Co3O4 nanoarrays that derived from zeolite imidazole framework (ZIF) on carbon cloth as ?fixed piles? for the in-situ solvothermal synthesis of Ni-MOF nanosheets. As a result, the Ni-MOF nanosheets closely distribute on the surface of the carbon cloth with fluffy structure, which favors exposure of more active sites and rapid diffusion of electrolyte ions. The as-fabricated integrated composite electrode (Co3O4@Ni-MOF) delivers a good specific capacitance of 1416 F/g at the current density of 1 A/g, superior to the individual Co3O4 (410 F/g) and Ni-MOF electrode (690 F/g). Moreover, the specific capacitance can be kept at 90% of its original value after 3000 cycles. Based on these advantages, a hybrid supercapacitor fabricated by the Co3O4@Ni-MOF electrode and activated carbon (AC) shows prominent energy density of 68.6 Wh kg-1 at the power density of 510 W kg-1, and excellent cycling stability (about 12% capacitance loss after 5000 charge-discharge cycles).
引用
收藏
页码:14001 / 14008
页数:8
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