Title of article :
Synthesis of Co(OH)2/graphene/Ni foam nano-electrodes with excellent pseudocapacitive behavior and high cycling stability for supercapacitors
Author/Authors :
Zhao، نويسنده , , Cuimei and Wang، نويسنده , , Xin and Wang، نويسنده , , Shumin and Wang، نويسنده , , Yayu and Zhao، نويسنده , , Yunxiao and Zheng، نويسنده , , Weitao، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2012
Pages :
7
From page :
11846
To page :
11852
Abstract :
Vertically aligned graphene nanosheets have been synthesized by radio-frequency plasma-enhanced chemical vapor deposition on nickel-foam current collectors and that have been used as substrates for cathodic electrodeposition of cobalt hydroxide nanosheets in Co(NO3)2 aqueous solution. Raman spectrum exhibits that high-quality graphene nanosheets have been synthesized. The composites have been characterized by X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy, cyclic voltammetry and galvanostatic charge/discharge. It indicates that hexagonal Co(OH)2 has a network microstructure, consisting of interlaced sheets with the thickness of 12 nm coated on the graphene nanosheets. The binder-free nano-electrode exhibits excellent pseudocapacitive behavior with pseudocapacitances of 693.8 and 506.2 Fg−1 at current density of 2 and 32 Ag−1, respectively, in a potential range of −0.1–0.45 V. The capacitance can retain about 91.9% after 3000 charge–discharge cycles at 40 Ag−1, which is higher than that of Co(OH)2/Ni foam (after 2000 cycles, 75.5% of initial capacitance remains). The introduction of graphene between Co(OH)2 and Ni foam demonstrates an enhancement of electrochemical stability of the nano-electrodes.
Keywords :
Cobalt hydroxide , Graphene nanosheet , plasma-enhanced chemical vapor deposition , Supercapacitor , Electrodeposition
Journal title :
International Journal of Hydrogen Energy
Serial Year :
2012
Journal title :
International Journal of Hydrogen Energy
Record number :
1672551
Link To Document :
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