Electroreduction of oxygen on nitrogen-doped graphene oxide supported silver nanoparticles
Nitrogen-doped graphene oxide supported silver nanoparticles (Ag/NGO) have been synthesised using three different methods. The prepared catalysts were studied by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and electrochemically t...
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Published in | Journal of electroanalytical chemistry (Lausanne, Switzerland) Vol. 794; pp. 197 - 203 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier B.V
01.06.2017
Elsevier Science Ltd |
Subjects | |
Online Access | Get full text |
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Summary: | Nitrogen-doped graphene oxide supported silver nanoparticles (Ag/NGO) have been synthesised using three different methods. The prepared catalysts were studied by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and electrochemically tested for oxygen reduction reaction (ORR) in alkaline solution. The Ag/NGO catalysts prepared by borohydride reduction showed the least degree of nanoparticle agglomeration and the material which was prepared using ascorbic acid yielded the biggest Ag particles. XPS revealed that the nitrogen to carbon atomic ratio was about 0.07 and EDS mapping showed that nitrogen was uniformly distributed over the graphene. The ORR on all the Ag/NGO catalysts proceeded via 4-electron pathway yielding water while on the support material, N-doped graphene oxide, the number of electrons transferred per O2 molecule was lower than four. The mass activity of all Ag/NGO catalysts was determined to be at least twice higher than that of NGO.
•Nitrogen-doped graphene supported Ag nanoparticles were synthesised and tested for ORR.•AgNPs supported on N-doped graphene showed excellent ORR performance in alkaline media.•The ORR on Ag/NGO catalysts follows a four-electron pathway.•Similar Tafel behaviour for O2 reduction was observed for Ag/NGO catalysts and bulk Ag. |
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ISSN: | 1572-6657 1873-2569 |
DOI: | 10.1016/j.jelechem.2017.04.022 |