B. Ruíz-Camacho, M. Valenzuela, J. A. Pérez-Galindo, F. Pola, M. Miki-Yoshida, N. Alonso‐Vante, R. González-Huerta
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引用次数: 6
Abstract
Pt/C catalysts supported on carbon (5 wt.% Pt) synthesized by photo-deposition and impregnation methods were electrochemi- cally evaluated in the oxygen reduction reaction. Platinum nanoparticles were prepared by photo-irradiation of Pt precursors (H2PtCl6 and C10H14O4Pt) with UV-irradiation (365 nm) at room temperature. The photo-reduction of H2PtCl6 to metallic platinum (Pt4+→Pt2+→Pt0) was faster than C10H14O4Pt (Pt2+→Pt0) at the same operation conditions. The Pt/C samples were characterized by XRD, EDS, H2 chemisorption, TEM, cyclic and linear voltammetry techniques. XRD and TEM/EDS studies showed that Pt particles synthesized with C10H14O4Pt by the photo-deposition method were smaller with a higher dispersion on carbon than those prepared with H2PtCl6. A similar behavior was found when the impregnation method is used. The platinum particle size was smaller with C10H14O4Pt as compared to H2PtCl6 precursor. The Pt/C catalyst synthesized with C10H14O4Pt by the photo-deposition method displayed a catalytic activity in the oxy- gen reduction reaction comparable to a commercial 10 wt. % Pt/C, ETEK catalyst.
期刊介绍:
This international Journal is intended for the publication of original work, both analytical and experimental, and of reviews and commercial aspects related to the field of New Materials for Electrochemical Systems. The emphasis will be on research both of a fundamental and an applied nature in various aspects of the development of new materials in electrochemical systems.