Issue 22, 2012

Platinum nanoflowers supported on graphene oxide nanosheets: their green synthesis, growth mechanism, and advanced electrocatalytic properties for methanol oxidation

Abstract

This paper reports a nontoxic, rapid, one-pot and template-free synthesis of three-dimensional (3D) Pt nanoflowers (PtNFs) with high yield and good size monodispersity supported on graphene oxide (GO) nanosheets. The key synthesis strategy employed a low-cost, green solvent, ethanol as the reductant and an advanced, powerful 2D carbon material, GO nanosheets as the stabilizing material. The resulting PtNFs-GO nanosheets were characterized by transmission electron microscopy (TEM), high-resolution TEM, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and electrochemical techniques. It was found that the monodispersed, porous PtNFs supported on GO nanosheets were a uniform size of 30 nm and each was composed of numerous “clean” and small (4 nm) Pt nanoparticles, which revealed an unusually high activity for methanol oxidation reaction compared to commercial Pt black. Furthermore, based on a systematic study of the PtNFs growth conditions, a possible mechanism, and especially the importance of GO in the formation was proposed. Our study demonstrates that GO is a promising support material for developing next-generation advanced Pt based fuel cells and their relevant electrodes in the field of energy.

Graphical abstract: Platinum nanoflowers supported on graphene oxide nanosheets: their green synthesis, growth mechanism, and advanced electrocatalytic properties for methanol oxidation

Supplementary files

Article information

Article type
Paper
Submitted
23 Feb 2012
Accepted
04 Apr 2012
First published
04 Apr 2012

J. Mater. Chem., 2012,22, 11284-11289

Platinum nanoflowers supported on graphene oxide nanosheets: their green synthesis, growth mechanism, and advanced electrocatalytic properties for methanol oxidation

X. Chen, B. Su, G. Wu, C. J. Yang, Z. Zhuang, X. Wang and X. Chen, J. Mater. Chem., 2012, 22, 11284 DOI: 10.1039/C2JM31133J

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