Facile chemical synthesis of nitrogen-doped graphene sheets and their electrochemical capacitance
To improve the electrochemical performance of graphene materials, nitrogen-doped graphene sheets (NGS) were simultaneously reduced and functionalized with nitrogen (N) doping from graphene oxide (GO) by a simple process using 1 wt.% ammonia water solution as the reducing agent, nitrogen precursor an...
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Veröffentlicht in: | Journal of power sources 2013-11, Vol.241, p.460-466 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | To improve the electrochemical performance of graphene materials, nitrogen-doped graphene sheets (NGS) were simultaneously reduced and functionalized with nitrogen (N) doping from graphene oxide (GO) by a simple process using 1 wt.% ammonia water solution as the reducing agent, nitrogen precursor and solvent. The NGS were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy–energy dispersive spectroscopy microanalysis, and differential scanning calorimetry. The thermal stability of NGS was much higher than that of GO. The N content in NGS was 4.4 at.% and a maximum specific capacitance up to 233.3 F g−1 was obtained at 0.5 A g−1. At 0.02 V s−1, the NGS exhibited a specific capacitance of 140.3 F g−1, which was over 8 times that of GO and nearly 2 times that of graphene without N-doping. These results revealed that N-doping of functional graphene provide remarkable improvements on the electrochemical capacitive performance of graphene materials. The NGS also showed high cycle stability of capacitive performance.
•N-doped graphene (NGS) is simultaneously reduced from GO and functionalised at 80 °C.•The reduction and N-doping of GO occur in 1 wt.% ammonia water at atmosphere pressure (101,325 Pa).•NGS has a N composition of 4.4 at.% and exhibits higher thermal stability than GO.•Specific capacitance of NGS is nearly twice that of RGO without N-doping.•NGS exhibits a maximum specific capacitance of 233.3 F g−1 and superior cycling stability. |
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ISSN: | 0378-7753 1873-2755 |
DOI: | 10.1016/j.jpowsour.2013.04.138 |