The electrooxidation of small organic molecules on platinum nanoparticles supported on gold: influence of platinum deposition procedure

Abstract

The electrocatalytic properties of small platinum nanoparticles were investigated for the oxidation of CO, methanol, and formic acid using voltammetry, chronoam- perometry, and surface-enhanced Raman spectroscopy. The particles were generated by galvanostatic deposition of platinum on a polished gold surface from an H2PtCl6 containing electrolyte and ranged between 10 and 20 nm in diameter for low platinum surface concentrations, 10 and 120 nm for medium concentrations, and full Pt monolayers for high concentrations. CO stripping and bulk CO oxidation experiments on the particles up to 120 nm in diameter displayed pronounced structural effects. The CO oxidation current-time transients show a current decay for low platinum coverages and a current maximum for medium and high coverages. These results were also observed in the literature for particles of 2- to 5-nm size and agglomerates of these particles. The similarities between the literature and our results, despite large differ- ences in particle size and morphology, suggest that particle structure and morphology are also very important catalytic parameters. Surface-enhanced Raman spectroscopy data obtained for the oxidation of CO on the Pt-modified Au electrodes corroborate this conclusion. A difference in the ratio between CO adsorbed in linear- and bridge-bonded positions on the Pt nanoparticles of different sizes demon- strates the influence of the surface morphology. The oxidation activity of methanol was found to decrease with the particle size, while the formic acid oxidation rate increases. Again, a structural effect is observed for particles of up to ca. 120 nm in diameter, which is much larger than the particles for which a particle size effect was reported in the literature. The particle shape effect for the methanol oxidation reaction can be explained by a reduction in available sites and a reduction in the mobility of CO formed by decomposition of methanol. As formic acid does not require Pt ensemble sites, decreasing the particle size, and thus, the relative number of defects, increases the reaction rate.