The influence of poisoning of MoO x ePt catalyst by CO on the kinetics of H 2 oxidation reaction (HOR) at MoO x ePt electrode in 0.5 mol dm À3 HClO 4 saturated with H 2 containing 100 ppm CO, was examined on rotating disc electrode (RDE) at 25 C. MoO x ePt nanocatalyst prepared by the polyole method
Heat treatment effect of Pt–V/C and Pt/C on the kinetics of the oxygen reduction reaction in acid media
✍ Scribed by L.G.R.A. Santos; K.S. Freitas; E.A. Ticianelli
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- English
- Weight
- 876 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0013-4686
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✦ Synopsis
This work studies the heat treatment effect of carbon-dispersed platinum and platinum-vanadium alloys on the kinetics of the oxygen reduction reaction (ORR) in acid medium. The catalyst powders were subjected to heat treatments at three temperatures for 1 h. The electronic and structural features of the materials were characterized by X-ray diffraction (XRD) and in situ X-ray absorption near edge structure (XANES). The XANES results for the oxidized state composites showed an increase of the Pt 5d band occupancy with increased heat treatment temperature for the Pt/C catalyst, while no changes were noted for Pt-V/C for the same treatments. The electrochemical characteristics for the ORR were investigated by cyclic voltammetry and state-state polarization measurements. The results showed that the ORR takes place by the multi-electronic charge transfer process, following a four electron mechanism. The kinetics of the ORR was evaluated using Tafel diagrams. It was observed that the ORR activity of the Pt/C and Pt-V/C is enhanced with the increase of the heat treatment temperature. The catalytic activity of the materials was analyzed in terms of the electronic and structural properties of Pt in the metallic particles.
📜 SIMILAR VOLUMES
Oxygen reduction on Pt supported on carbon black in PTFE-bonded porous electrodes in 98% H,PO, at 170°C was investigated. The influence of the Pt surface area and the volume of H,PO, in the electrode structure (per cent acid occupation, PAO) on the performance of porous electrodes (ie current-potent