Nitrogen and sulfur co-doped porous graphene aerogel as an efficient electrode material for high performance supercapacitor in ionic liquid electrolyte
Nitrogen and sulfur co-doped graphene aerogel (NS-GA) is prepared by one-pot process. The as-prepared materials are investigated as supercapacitors electrodes in an ionic liquid (1-ethyl-3-methylimidazolium tetrafluoroborate, EMIMBF4) electrolyte. The NS-GA is characterized using X-ray diffraction,...
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Published in | Journal of power sources Vol. 390; pp. 215 - 223 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
30.06.2018
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Subjects | |
Online Access | Get full text |
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Summary: | Nitrogen and sulfur co-doped graphene aerogel (NS-GA) is prepared by one-pot process. The as-prepared materials are investigated as supercapacitors electrodes in an ionic liquid (1-ethyl-3-methylimidazolium tetrafluoroborate, EMIMBF4) electrolyte. The NS-GA is characterized using X-ray diffraction, X-ray photoelectron spectroscopy, and Raman spectroscopy scanning electron microscopy. The results show that the NS-GA has hierarchical porous structure. Electrochemical performance is investigated by cycle voltammetry and galvanostatic charge-discharge. Notably, the supercapacitor based on the NS-GA-5 possesses a maximum energy density of 100.7 Wh kg−1 at power density of 0.94 kW kg−1. The electrode materials also offer a large specific capacitance of 203.2 F g−1 at a current density of 1 A g−1 and the capacitance retention of NS-GA-5 is 90% after 3000 cycles at a scan rate of 2 A g−1. The NS-GA-5 with numerous advantages including low cost and remarkable electrochemical behaviors can be a promising electrode material for the application of supercapacitors.
•A simple method is reported for synthesizing NS co-doped graphene aerogel.•The NS co-doped graphene aerogel shows the hierarchical structures.•The supercapacitors exhibit superior electrochemical performance.•The supercapacitors deliver a maximum energy density of 100.7 Wh kg−1. |
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ISSN: | 0378-7753 1873-2755 |
DOI: | 10.1016/j.jpowsour.2018.04.057 |