Issue 19, 2017

Two-step controllable preparation of NiO nanocrystal anchored reduced graphene oxide sheets and their electrochemical performance as supercapacitors

Abstract

A feasible and expandable two-step strategy for the preparation of reduced graphene oxide (rGO) supported NiO nanocrystals (rGO-NiO) was developed using graphene oxide (GO), nickel sulfate and ammonia as raw materials. The rGO-NiO composites were obtained with the benefit of electrostatic attraction between GO and Ni2+ (or Ni(OH)2) in a mild solution phase precipitation process and a sequent simultaneous thermal decomposition of Ni(OH)2 and reduction of GO in Ar. The influence of calcination temperature on the morphology, structure and electrochemical performance of the composites was investigated. The results show that the calcination temperature has less impact on the morphology of the composites. Homogenous cubic NiO nanocrystals (<10 nm) were well coated onto the surface of rGO both at 250 °C and 300 °C. However, the composites obtained at 300 °C (rGO-NiO 300) possess better crystallinity of NiO and a higher reduction degree of GO but lower specific surface area as well as pore volume compared with the composites achieved at 250 °C (rGO-NiO 250). rGO-NiO 250 is superior to rGO-NiO 300 in specific capacitance at all current densities (1044 vs. 422 F g−1 at 1 A g−1 and 600 vs. 360 F g−1 at 20 A g−1), but shows inferior rate capability (57.4% vs. 85.3% from 1 to 20 A g−1) and cycling stability (83% vs. 137% after 2000 cycles).

Graphical abstract: Two-step controllable preparation of NiO nanocrystal anchored reduced graphene oxide sheets and their electrochemical performance as supercapacitors

Supplementary files

Article information

Article type
Paper
Submitted
24 Jun 2017
Accepted
12 Aug 2017
First published
14 Aug 2017

New J. Chem., 2017,41, 10695-10702

Two-step controllable preparation of NiO nanocrystal anchored reduced graphene oxide sheets and their electrochemical performance as supercapacitors

J. Gui, J. Zhang, T. Liu, Y. Peng and J. Chang, New J. Chem., 2017, 41, 10695 DOI: 10.1039/C7NJ02267K

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