Effect of nitrogen precursors on the electrochemical performance of nitrogen-doped reduced graphene oxide towards oxygen reduction reaction

A series of nitrogen-doped reduced graphene oxides (NGs) with different ratios are synthesized by thermal annealing of graphene oxide with melamine or urea. The total nitrogen content in NG is high, with values of up to 5.88 at.%. The NG samples prepared by melamine exhibited thin transparent graphe...

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Veröffentlicht in:Journal of alloys and compounds 2016-08, Vol.677, p.112-120
Hauptverfasser: Soo, Li Ting, Loh, Kee Shyuan, Mohamad, Abu Bakar, Daud, Wan Ramli Wan, Wong, Wai Yin
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Sprache:eng
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Zusammenfassung:A series of nitrogen-doped reduced graphene oxides (NGs) with different ratios are synthesized by thermal annealing of graphene oxide with melamine or urea. The total nitrogen content in NG is high, with values of up to 5.88 at.%. The NG samples prepared by melamine exhibited thin transparent graphene sheets structure, with consist of higher nitrogen doping level and quaternary N content compared to those NG samples prepared from urea. Electrochemical characterizations show that NG is a promising metal-free electrocatalyst for an oxygen reduction reaction (ORR). Incorporation of nitrogen atoms into graphene basal plane can enhances its electrocatalytic activity toward ORR in alkaline media. The onset potential and mean number of electron transfers on NG 1 are −0.10 V and 3.80 respectively, which is higher than that of reduced graphene oxide (−0.15 V, 3.52). This study suggests that quaternary-N of the NG samples is the active site which determines the ORR activity Moreover, the NG samples with the transparent layer of graphene-like structure have better ORR performances than that of bulk graphite-like NG samples. [Display omitted] •Synthesis of nitrogen-doped graphene (NG) via thermal annealing.•The effects of the nitrogen precursors on the synthesized NG are discussed.•Electrochemical performances of the NG are correlated to N doping and EASA.•Graphitic-N is proposed to be the active site for ORR.
ISSN:0925-8388
1873-4669
DOI:10.1016/j.jallcom.2016.03.214