Anodic Oxidation of COads Derived from methanol on pt electrocatalysts linked to the bonding type and adsorption site
- Author(s): Engstrom, AM
- Lim, E
- Reimer, JA
- Cairns, EJ
- et al.
Published Web Locationhttps://doi.org/10.1016/j.electacta.2014.05.006
A newly formulated four-component modified Butler-Volmer model has been developed to evaluate global oxidation kinetic parameters for the various types of carbon monoxide adsorbates (COads) on a nanoparticle Pt surface determined by the type of bonding as well as the local structure of the adsorption site. Partial coverages of COadswere prepared by potentiostatic adsorption of methanol followed by potentiostatic partial oxidation at various elevated potentials and for various durations. Anodic linear sweep voltammetry was then performed, and the COadsoxidation peaks were fitted with the model to analyze the kinetics. According to the model, preferential oxidation with respect to COadsbonding and Pt substrate structure can be achieved dependent upon the potential and extent of oxidation. Partial oxidation at 450 mV vs. RHE for 60 min. resulted in a majority population of linearly bonded COadson cubic-packed Pt sites; whereas partial oxidation at 650 mV vs. RHE for 220 sec. resulted in a majority population of bridged-bonded COadson close-packed Pt sites. © 2014 Elsevier Ltd.
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