Abstract

The effect of palladium- and ruthenium-based clusters on nanocrystalline tin dioxide interaction with oxygen was studied by temperature-programmed oxygen isotopic exchange with mass-spectrometry detection. The modification of aqueous sol–gel prepared SnO<sub>2</sub> by palladium and, to a larger extent, by ruthenium, increases surface oxygen concentration on the materials. The revealed effects on oxygen exchangelowering the threshold temperature, separation of surface oxygen contribution to the process, increase of heteroexchange rate and oxygen diffusion coefficient, decrease of activation energies of exchange and diffusionwere more intensive for Ru-modified SnO<sub>2</sub> than in the case of SnO<sub>2</sub>/Pd. The superior promoting activity of ruthenium on tin dioxide interaction with oxygen was interpreted by favoring the dissociative O<sub>2</sub> adsorption and increasing the oxygen mobility, taking into account the structure and chemical composition of the modifier clusters

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