AVS 49th International Symposium
    Electrochemistry and Fluid-Solid Interfaces Monday Sessions
       Session EC+SS-MoM

Invited Paper EC+SS-MoM5
Strategies for the Study of Methanol and CO Electrocatalysis on Solid Electrodes and Nanometer-Scale Supported Catalysts

Monday, November 4, 2002, 9:40 am, Room C-104

Session: Fuel Cells and Surface Electrochemical Reactions
Presenter: C. Korzeniewski, Texas Tech University
Authors: C. Korzeniewski, Texas Tech University
G. Vijayaraghavan, Texas Tech University
L. Gao, Texas Tech University
Correspondent: Click to Email

The electrochemical oxidation of methanol and related small molecules has been of special interest in relation to fuel cell research. The development of fuel cells that operate below 100 °C on methanol, or H@sub 2@ has stimulated interest in the reaction steps involved in methanol and carbon monoxide oxidation at metal electrodes. In addition to being a by-product of methanol oxidation, carbon monoxide can also be present as an impurity in H@sub 2@. Adsorption of carbon monoxide on the anode catalyst generally degrades its performance. We have approached the study of methanol and carbon monoxide oxidation with the use of electrochemical techniques in combination with in situ infrared spectroscopy, atomic force microscopy (AFM) and wet-analytical methods. This presentation will focus on the surface electrochemistry of methanol and carbon monoxide at supported Pt and Pt-Ru catalysts. In situ infrared measurements are being performed with Vulcan carbon supported fuel cell catalysts. The carbon supported materials are adsorbed onto a smooth gold electrode to enable infrared sampling in a standard reflectance geometry. A thermostatted cell allows in situ infrared measurements between ambient and 80 °C. Similar to the bulk metals, thermal effects on methanol oxidation at nanometer-scale catalysts are stronger for Pt-Ru (atomic percent Ru = 50%) than Pt. The influence that metal particle size distribution and spatial arrangement on carbon supports has on methanol oxidation pathways is being investigated by depositing metal particles on highly ordered pyrolytic graphite. The surface electrocatalytic properties of the supported particles are investigated with cyclic voltammetry. AFM is used to determine the catalyst size distribution and spatial arrangement at different stages of preparation and electrochemical characterization. Properties of nanometer-scale metal particles in relation to methanol oxidation pathways will be discussed.