4.6 Article

Decoration of Pd and Pt nanoparticles on a carbon nitride (C3N4) surface for nitro-compounds reduction and hydrogen evolution reaction

Journal

NEW JOURNAL OF CHEMISTRY
Volume 41, Issue 18, Pages 9658-9667

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7nj01221g

Keywords

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Funding

  1. Department of Science and Technology (DST) Science and Engineering Research Board (SERB) Fast-track grant, Government of India [SB/FT/CS-042/2012]
  2. University Grants Commission (UGC) special assistance program, Government of India
  3. DST-FIST program, Government of India
  4. Department of Science and Technology (DST) Inspire program [DST/INSPIRE/04/2015/00039]
  5. DST-FIST

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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(-2) vs. 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(-2) vs. 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 x 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.

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