NiO/Ni Metal-Organic Framework Nanostructures for Asymmetric Supercapacitors

被引:61
|
作者
Wang, Guosheng [1 ]
Yan, Zhaoxiong [1 ]
Wang, Nenghuan [1 ]
Xiang, Ming [1 ]
Xu, Zhihua [1 ]
机构
[1] Jianghan Univ, Minist Educ, Key Lab Optoelect Chem Mat & Devices, Wuhan 430056, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
metal-organic framework; NiO; nanocomposites; supercapacitor; energy storage; battery-type materials; MICROWAVE-ASSISTED SYNTHESIS; PSEUDO-CAPACITIVE MATERIAL; NICO-MOF NANOSHEETS; CATHODE MATERIAL; PERFORMANCE; NICKEL; ANODE; ALPHA-NI(OH)(2); MICROSPHERES; FABRICATION;
D O I
10.1021/acsanm.1c01628
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
An electrode material with high performance as a key part is highly desirable for supercapacitors. Herein, NiO/Ni metal-organic framework (Ni-MOF) composites were successfully synthesized via the first preparation of NiO nanoflakes and then in situ formation of Ni-MOF over NiO. Particularly, the conversion degree of Ni-MOF from NiO was conveniently tuned by altering the amount of terephthalic acid added in the hydrothermal process. NiO/Ni-MOF-25 with 25% of the conversion ratio of NiO to Ni-MOF possessed superior electrochemical performance with a specific capacity of 163.4 mA h (1176.6 F g(-1) ) at a current density of 1 A g(-1), higher than Ni-MOF (79.3 mA h g(-1)) and NiO (79.8 mA h g(-1)). The boosted electrochemical performance of NiO/Ni-MOF-25 was attributed to its core-shell configuration, relatively high specific surface area, and enhanced electrical conductivity. The assembled NiO/Ni-MOF-25//activated carbon asymmetrical supercapacitor achieved a maximum energy density of 31.3 W h kg(-1) at a power density of 374.2 W kg(-1) and decent cyclic durability with 88.7% of incipient capacitance after 2000 cycles. Moreover, two asymmetric devices in series constructed 3 months ago could efficiently illuminate a green light-emitting diode (LED) lamp. This work offers a facile way to rationally design and synthesize composite electrode materials for powerful supercapacitors.
引用
收藏
页码:9034 / 9043
页数:10
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