|
Researchspace >
General science, engineering & technology >
General science, engineering & technology >
General science, engineering & technology >
Please use this identifier to cite or link to this item:
http://hdl.handle.net/10204/3269
|
| Title: | Effect of P on the electrochemical activity of carbon supported Pt-Ru alloy catalyst for methanol oxidation. |
| Authors: | Mohlala, M Modibedi, M Mathe, MK |
| Keywords: | Methanol electrooxidation Phosphor Ruthenium Linear chronoamperometry |
| Issue Date: | Nov-2007 |
| Publisher: | Catalysis Society of South Africa (CATSA) 2007 |
| Citation: | Mohlala, M, Modibedi, M and Mathe, MK. 2007. Effect of P on the electrochemical activity of carbon supported Pt-Ru alloy catalyst for methanol oxidation. Catalysis Society of South Africa (CATSA) Conference. Richards Bay, South Africa, 11-14 November 2007, pp 1 |
| Abstract: | In polymer electrolyte membrane fuel cell (PEMFC), platinum is recognized to be the most active metal for methanol oxidation, however there is a strong CO adsorption tendency, which blocks the surface for further methanol adsorption and leads to very low power densities [1, 2]. Pt-Ru and Pt-Sn are the most promising of the binary catalysts for methanol and ethanol oxidation respectively due to the improved CO tolerance. On the other hand, the power densities of Pt-Ru and Pt-Sn anode catalysts for direct alcohol fuel cell is lower than that of the hydrogen PEMFC [3, 4, and 5]. This study aims at improving the performance of the binary catalyst through the addition of phosphorus group following the sodium hypophosphite method [6]. The optimum amount of phosphorus on the Pt-Ru/C, Pt-Sn/C and Pt-Ir/C was investigated by measuring the activity of the catalysts for methanol electrooxidation with cyclic voltammetry and linear chronoamperometry |
| Description: | Catalysis Society of South Africa (CATSA) Conference. Richards Bay, South Africa, 11-14 November 2007 |
| URI: | http://hdl.handle.net/10204/3269 |
| Appears in Collections: | General science, engineering & technology
|
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
|