February 1, 2008
Journal Article

Interaction of Carbon Dioxide with Cu Overlayers on Pt(111)

Abstract

The research described in this product was performed in part in the Environmental Molecular Sciences Laboratory, a national scientific user facility sponsored by the Department of Energy's Office of Biological and Environmental Research and located at Pacific Northwest National Laboratory. Experimental and theoretical studies on the interaction of carbon dioxide with pseudomorphic and rough copper layers deposited on a platinum (111) single crystal are reported. Evidence for carbon dioxide dissociation and carbonate formation is presented and the relevance to methanol synthesis is discussed. Intermediate species on the surfaces were identified using in situ polarization modulation infrared reflection absorption spectroscopy (PM-IRRAS) at pressures up to ~550 mbar and electron energy loss spectroscopy (EELS) in ultra-high vacuum. Temperature programmed desorption (TPD) reveals a broad high temperature desorption state for CO2 with peak maximum around 450 K. X-ray photoelectron spectroscopy (XPS) shows that approximately one third of the oxygen accumulated on the surface upon CO2 exposure remains after TPD, indicative of carbonate formation via CO2 dissociation supplying Oads and then facile CO2+Oads association, as well as subsequent decomposition at higher temperatures. Density functional theory studies of stepped Cu and Cu/Pt slabs reproduce vibrational frequencies of the carbonate, suggesting a nearly flat tridentate configuration at steps/defect sites.

Revised: April 7, 2011 | Published: February 1, 2008

Citation

Schumacher N., K.J. Andersson, L.C. Grabow, M. Mavrikakis, J. Nerlov, and I. Chorkendorff. 2008. Interaction of Carbon Dioxide with Cu Overlayers on Pt(111). Surface Science 602, no. 3:702-711. doi:10.1016/j.susc.2007.11.030