Issue 13, 2014

Supercritical fluid assisted synthesis of N-doped graphene nanosheets and their capacitance behavior in ionic liquid and aqueous electrolytes

Abstract

N-doped graphene nanosheets (N-doped GNS) were obtained by a single step supercritical fluid assisted reaction of N-containing organic compounds with graphene oxide (GO) solution. A N-doped GNS sample shows capacitances of 280 F g−1 in aqueous 1 M H2SO4 (0.9 V) and 104 F g−1 in ionic liquid EMI-TFSA (3.6 V). A NE-GNS electrode shows energy densities of 8 W h kg−1 and 40 W h kg−1 in 1 M H2SO4 and EMI-TFSA, respectively. The nature of chemical bonding and the amount of N doping in the graphene samples were estimated by XPS spectroscopy. The amount of N-doping varies with the nature of the N-containing organic compounds and the supercapacitance behaviour depends on the amount of N-doping as well as the nature of N-doping in the graphene. TEM, FE-SEM images and Raman spectroscopic characterization reveals the presence of few-layer N-doped GNS. FT-IR spectra exhibit the presence of various functional groups on N-doped GNS. XRD diffraction analysis showed the weakly stacked N-doped GNS due to the N-doping and the presence of N-containing functional groups on N-doped GNS. The cyclic voltammetry studies showed the capacitance behaviour of N-doped GNS electrodes at a high potential window of 4.25 V in ionic liquids. The charge–discharge profile showed the stable charge–discharge behaviour of the N-doped GNS electrodes.

Graphical abstract: Supercritical fluid assisted synthesis of N-doped graphene nanosheets and their capacitance behavior in ionic liquid and aqueous electrolytes

Supplementary files

Article information

Article type
Paper
Submitted
11 Dec 2013
Accepted
05 Jan 2014
First published
08 Jan 2014

J. Mater. Chem. A, 2014,2, 4731-4738

Author version available

Supercritical fluid assisted synthesis of N-doped graphene nanosheets and their capacitance behavior in ionic liquid and aqueous electrolytes

M. Sathish, S. Mitani, T. Tomai and I. Honma, J. Mater. Chem. A, 2014, 2, 4731 DOI: 10.1039/C3TA15136K

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