Preparation and characterization of Pt/C and Ptsingle bondRu/C electrocatalysts for direct ethanol fuel cells

Nano-sized Pt and Ptsingle bondRu colloids are prepared by a microwave-assisted polyol process, and transferred to a toluene solution of decanthiol. Vulcan XC-72 is then added to the toluene solution to adsorb the thiolated Pt and Ptsingle bondRu colloids. Transmission electron microscopy examinations show nearly spherical particles and narrow size distributions for both supported and unsupported metals. The carbon-supported Pt and Ptsingle bondRu nanoparticles are activated by thermal treatment to remove the thiol stabilizing shell. All Pt and Ptsingle bondRu catalysts (except Pt23single bondRu77) give the X-ray diffraction pattern of a face-centered cubic (fcc) crystal structure, whereas the Pt23single bondRu77 alloy is more typical of the hexagonal close packed (hcp) structure. The electro-oxidation of liquid ethanol on these catalysts is investigated at room temperature by cyclic voltammetry. The results demonstrate that the alloy catalyst is catalytically more active than pure platinum. Preliminary tests on a single cell of a direct ethanol fuel cell (DEFC) indicate that a Pt52single bondRu48/C anode catalyst gives the best electrocatalytic performance among all the carbon-supported Pt and Ptsingle bondRu catalysts.