Issue 1, 2012

Nucleation reaction dynamics of Pt nanoparticles observed by the heterodyne transient grating method

Abstract

The nucleation reaction dynamics of platinum nanoparticles in the photoreduction process of H2Pt(IV)Cl6 solution were investigated by the heterodyne transient grating (HD-TG) method. The formation mechanism of platinum nanoparticles was considered, supported by information obtained from UV/VIS absorption spectroscopy during the reaction and SEM images of the generated nanoparticles. In particular, the roles of poly(N-vinyl-2-pyrrolidone) (PVP) as a protective polymer and ethanol as a solvent were studied. The chemical species involved in the reaction can be identified from the diffusion coefficients obtained from HD-TG measurements; the species observed by UV pulse irradiation were assigned to H2Pt(IV)Cl6 as a reactant species and H2Pt(II)Cl4 and Pt nuclei as product species. It was observed that the amounts of the reactant and product species increased, and many homogeneous nanoparticles were generated, by an increase in PVP concentration. The addition of ethanol to the solvent showed a larger effect on the enhancement of the reduction of H2Pt(IV)Cl6 than that of PVP; however, it did not lead to Pt nuclei formation in the order of seconds. Nevertheless, because nanoparticle formation was confirmed by UV/VIS absorption spectroscopy and SEM images, the formation of nanoparticles following nuclei formation must have proceeded via a slow reaction. Therefore, nucleation and nanoparticle formation are considered to occur on a longer time scale than 10 s in water/ethanol solvent.

Graphical abstract: Nucleation reaction dynamics of Pt nanoparticles observed by the heterodyne transient grating method

Article information

Article type
Paper
Submitted
13 Sep 2011
Accepted
24 Oct 2011
First published
10 Nov 2011

Phys. Chem. Chem. Phys., 2012,14, 200-204

Nucleation reaction dynamics of Pt nanoparticles observed by the heterodyne transient grating method

N. Maeda, T. Eitoku, Y. Ikezoe and K. Katayama, Phys. Chem. Chem. Phys., 2012, 14, 200 DOI: 10.1039/C1CP22909E

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