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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/3229
Title: Decoration of Pd and Pt nanoparticles on a carbon nitride (C3N4) surface for nitro-compounds reduction and hydrogen evolution reaction
Authors: Basu, Mrinmoyee
Gangopadhyay, Subhashis
Pande, Surojit
Keywords: Chemistry
Nanoparticles
Nitro-compounds reduction
Hydrogen
Issue Date: 2017
Publisher: RSC
Abstract: Herein, 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.
URI: https://pubs.rsc.org/en/content/articlelanding/2017/nj/c7nj01221g
http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3229
Appears in Collections:Department of Chemistry

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