Durable Transition-Metal-Carbide-Supported Pt–Ru Anodes for Direct Methanol Fuel Cells
✍ Scribed by K. G. Nishanth; P. Sridhar; S. Pitchumani; A. K. Shukla
- Publisher
- John Wiley and Sons
- Year
- 2012
- Tongue
- English
- Weight
- 483 KB
- Volume
- 12
- Category
- Article
- ISSN
- 1615-6846
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Molybdenum carbide (MoC) and tungsten carbide (WC) are synthesized by direct carbonization method. Pt–Ru catalysts supported on MoC, WC, and Vulcan XC‐72R are prepared, and characterized by X‐ray diffraction, X‐ray photoelectron spectroscopy, and transmission electron microscopy in conjunction with electrochemistry. Electrochemical activities for the catalysts towards methanol electro‐oxidation are studied by cyclic voltammetry. All the electro‐catalysts are subjected to accelerated durability test (ADT). The electrochemical activity of carbide‐supported electro‐catalysts towards methanol electro‐oxidation is found to be higher than carbon‐supported catalysts before and after ADT. The study suggests that Pt–Ru/MoC and Pt–Ru/WC catalysts are more durable than Pt–Ru/C. Direct methanol fuel cells (DMFCs) with Pt–Ru/MoC and Pt–Ru/WC anodes also exhibit higher performance than the DMFC with Pt–Ru/C anode.
📜 SIMILAR VOLUMES
The electrooxidation of methanol on porous carbon electrodes impregnated with bimetallic platinum group catalysts, Pt/M (M = Au, OS, Ir, Pd and Ru), in a H,SO, electrolyte is reported. Both Au and Pd are found to inhibit the reaction while Ir, OS and Ru act as promotors. The presence of metal oxides
## Abstract Pt~44~Ru~41~Os~10~Ir~5~ anode electro‐catalysts for direct methanol fuel cells with a high specific surface area are synthesized by the complexed sol—gel process from Pt(acac)~2~, Ru(acac)~3~, Ir(acac)~3~, OsCl~3~, and Me~4~NOH in acetone/MeOH.
## Abstract A new principle for designing catalyst supports with water activation ability was proposed. According to this principle, stabilized nickel(+3) oxides with different dopants were tested as possible support and promoter for Pt catalyst in direct methanol fuel cells. It was found that the