The effect of electrochemical promotion of catalysis was investigated for the water-gas shift reaction over porous Pt catalyst electrodes interfaced with 8%mol Yttria-stabilized Zirconia. A fuel cell type electrochemical reactor was used at temperatures from 300 °C to 400 °C, under PH2O/ PCO ratio values from 2.85 to 31. A negative order dependence of the catalytic reaction rate on PCO and a positive one on PH2O was found under open-circuit and polarization conditions. Positive potential application (+2.5 V), i.e., O2- supply to the catalyst surface, causes a small decrease in the catalytic reaction rate, while negative potential application (-1.5 V) results in a pronounced rate increase, up to 200%, with apparent faradaic efficiency values up to 110. The rate increase obtained with negative polarization can be attributed to the weakening of the Pt-CO bond strength but also, to the increase in surface concentration of oxygen ion vacancies near the Pt-gas-support three-phase boundaries necessary for water dissociation. © 2011 Elsevier Inc. All rights reserved.
CITATION STYLE
Souentie, S., Lizarraga, L., Kambolis, A., Alves-Fortunato, M., Valverde, J. L., & Vernoux, P. (2011). Electrochemical promotion of the water-gas shift reaction on Pt/YSZ. Journal of Catalysis, 283(2), 124–132. https://doi.org/10.1016/j.jcat.2011.07.009
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