Selectivity loss of Pt/CeO2 PROX catalysts at low CO concentrations: mechanism and active site study

CO and H2 oxidation were studied over a series of Pt/CeO2 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 O2 concentrations and explains the transition from L–H to M–vK reaction character. Redox site measurements are performed on Pt/CeO2 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.

A dual pathway mechanism for CO and H2 oxidation on Pt/CeO2 is proposed and evaluated. Reaction selectivity depends heavily on the prevalent dominant pathway.Figure optionsDownload high-quality image (92 K)Download as PowerPoint slide