Selectivity loss of Pt/CeO_2 PROX catalysts at low CO concentrations: Mechanism and active site study

摘要

CO and H_2 oxidation were studied over a series of Pt/CeO _2 catalysts with differing Pt loadings and dispersions. Kinetic rate analysis confirms the presence of dual Langmuir-Hinshelwood (L-H) and Mars and van Krevelen (M-vK) pathways and is used to explain the loss in CO oxidation selectivity at low CO concentrations. In situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) shows the strong CO coverage dependence on both CO and O_2 concentrations and explains the transition from L-H to M-vK reaction character. Redox site measurements are performed on Pt/CeO_2 catalysts by anaerobic titrations under conditions where the M-vK pathway dominates the reaction rate. Similar redox site densities per interfacial Pt atom suggest that interfacial Pt-O-Ce sites are responsible for M-vK redox activity.