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Pt nanoparticles supported on NiTiO3/C as electrocatalyst towards high performance Methanol Oxidation Reaction
Authors:Velumani Thiagarajan  Ramasamy Manoharan  Palaniswamy Karthikeyan  Eliyan Nikhila  A. Hernández-Ramírez  F.J. Rodriguez-Varela
Affiliation:1. Electrochemical Energy Materials Laboratories, Nanotech Research Innovation and Incubation Centre, PSG Institute of Advanced Studies, Avinashi Road, Peelamedu, Coimbatore, 641 004, India;2. Programa de Nanociencias y Nanotecnología, Cinvestav Unidad Saltillo, Av. Industria Metalúrgica 1062, Parque Industrial Ramos Arizpe, Ramos Arizpe, Coahuila, C.P. 25900, Mexico;3. Grupo de Sustentabilidad de los Recursos Naturales y Energía, Cinvestav Unidad Saltillo, Av. Industria Metalúrgica 1062, Parque Industrial Ramos Arizpe, Ramos Arizpe, Coahuila, C.P. 25900, Mexico
Abstract:Pt nanoparticles supported on NiTiO3/C has been synthesized by a wet chemical method, using the corresponding metal precursors and citric acid as a complexing reagent. The nanocomposite has been characterized using X-ray diffraction (XRD), Transmission Electron Microscope (TEM) and X-ray Photoelectron Spectroscopy (XPS) respectively. The electrocatalytic Methanol Oxidation Reaction (MOR) has been performed using Pt-NiTiO3/C catalyst in both alkaline and acid medium. Analysis using cyclic voltammetry (CV), steady state polarization (SSP), and chronoamperometry (CA) techniques clearly demonstrate that Pt-NiTiO3/C catalyst exhibits higher performance in methanol oxidation in alkaline medium compared to acid medium. The results demonstrate that NiTiO3 has significant promotion effect on the electrocatalytic activity and stability for the methanol electro-oxidation. The enhanced activity is attributed to the ability of NiTiO3 to promote COads oxidation through strong interaction with Pt (which is in close proximity to NiTiO3). Pt-NiTiO3/C appears to be a promising anode catalyst for direct methanol fuel cells.
Keywords:Electrocatalytic activity  Platinum-nickel titanate  Methanol electro-oxidation  Electrochemical surface area  Promotion effect
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