Fabrication, annealing, and electrocatalytic properties of platinum nanoparticles supported on self-

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The platinum nanoparticles supported on self-organized TiO2 nanotubes (Pt-TiO2/Ti) were prepared using electrochemical anodic oxidation followed by cathodic reduction. The structure and chemical nature of the Pt-TiO2/Ti electrocatalyst were investigated by X-ray diffraction (XRD) and scanning electron microscopy (SEM). Both XRD and SEM results indicate the presence of platinum on nanotubular TiO2. The stability of the Pt deposits was also investigated in 0.5 mol/L H2SO4 solution by cyclic voltammetry. The electrocatalytic activity of the Pt-TiO2/Ti catalyst exhibits enhancement effect during electro-oxidation of methanol when annealed to anatase. Successive cyclic voltammograms of methanol oxidation on the Pt-TiO2/Ti electrocatalyst shows unique electrocatalytic characteristics when compared to methanol oxidation on the bulk Pt catalyst. This is because of further quick oxidation of adsorbed CO by Pt (111) facets of Pt particles on self-organized TiO2 nanotubes when the formation of an electroactive film onto the working catalyst surface occurs. The structure and chemical nature of the Pt-TiO2 / Ti electrocatalyst were investigated by X-ray diffraction (XRD Both scanning electron microscopy (SEM). Both XRD and SEM results indicate the presence of platinum on nanotubular TiO2. The stability of the Pt deposits was also investigated in 0.5 mol / L H2SO4 solution by cyclic voltammetry. The electrocatalytic activity of the Pt- TiO2 / Ti catalyst exhibits enhancement effect during electro-oxidation of methanol when annealed to anatase. Successive cyclic voltammograms of methanol oxidation on the Pt-TiO2 / Ti electrocatalyst shows unique electrocatalytic characteristics when compared to methanol oxidation on the bulk Pt catalyst. of further quick oxidation of adsorbed CO by Pt (111) facets of Pt particles on self-organized TiO2 nanotubes when the formation of an electroactive film onto the working catalyst surface occurs.
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