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dc.contributor.authorBasu, Mrinmoyee-
dc.contributor.authorGangopadhyay, Subhashis-
dc.contributor.authorPande, Surojit-
dc.date.accessioned2021-11-11T10:45:01Z-
dc.date.available2021-11-11T10:45:01Z-
dc.date.issued2017-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2017/nj/c7nj01221g-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3229-
dc.description.abstractHerein, we propose the synthesis of Pd and Pt monometallic nanoparticles on a carbon nitride (C3N4) surface for the reduction of nitro compounds as well as for electrocatalysis. For the synthesis of C3N4/Pd and C3N4/Pt, metal ions were initially adsorbed on the C3N4 surface and then subsequently reduced by NaBH4. The as-synthesized heterostructures were authenticated by different characterization techniques: UV-vis, PXRD, XPS, TEM, FESEM, and EDS. Decorations of monometallic NPs on C3N4 not only improved the reduction efficiency of nitro-compounds but also enhanced the electrocatalytic activity in the hydrogen evolution reaction. C3N4/Pt proved to be an efficient electrocatalyst as it requires a potential of −0.339 V to attain a current density of 10 mA cm−2; whereas, C3N4/Pd requires −0.371 V to reach a current density of 10 mA cm−2vs. Ag/AgCl. Both C3N4/Pd and Pt heterostructures are better than bare C3N4, which needs −0.596 V to achieve a current density of 10 mA cm−2vs. Ag/AgCl. On the other hand, C3N4/Pd showed a better performance in nitro-compound reduction compared to C3N4/Pt and bare C3N4. The kinetic study reveals that the rate constant using a C3N4/Pd catalyst is 6.7 × 10−1 min−1 for p-nitroaniline reduction, which is 101 times higher compared to bare C3N4 and 4.7 times higher in comparison to C3N4/Pt.en_US
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectNanoparticlesen_US
dc.subjectNitro-compounds reductionen_US
dc.subjectHydrogenen_US
dc.titleDecoration of Pd and Pt nanoparticles on a carbon nitride (C3N4) surface for nitro-compounds reduction and hydrogen evolution reactionen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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