The Reaction of Carbon Monoxide with Palladium Supported on Cerium Oxide Thin Films

Journal Article · Mon Jan 01 04:00:00 EST 2007 · Surface Science

DOI:https://doi.org/10.1016/j.susc.2007.05.037· OSTI ID:931761

Senanayake, Sanjaya D ^[1]; Zhou, Jing ^[1]; Baddorf, Arthur P ^[1]; Mullins, David R ^[1]

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1. ORNL

In this study we probe the reaction of carbon monoxide with Pd nanoparticles supported on cerium oxide thin films. With the use of soft X-ray photoelectron spectroscopy (sXPS), and temperature programmed desorption (TPD) the surface intermediates and pathways leading to reaction products of CO on Pd supported on ceria were investigated. When Pd is supported on the stoichiometric CeO{sub 2} surface (Ce{sup +4}) only the molecular adsorption of CO on Pd is visible (286.4 eV). All of the CO desorbs below 520 K, however a small amount of O exchange between the CO and the ceria was indicated through the acquisition of labeled {sup 18}O from the substrate in the desorbed CO. The Pd nanoparticles are activated on partially reduced CeOx to promote the dissociation of <10% of the CO as indicated by a C-Pd species (284.4 eV) in sXPS. The C recombines with O from the ceria and desorbs between 600 and 700 K. The majority of the CO does not dissociate, however, and the degree of dissociation does not increase with the degree of ceria reduction. This result is in contrast with Rh nanoparticles supported on ceria where the degree of dissociation increased with the degree of ceria reduction and nearly total dissociation was obtained when the ceria was highly reduced.

• Research Organization: Oak Ridge National Laboratory (ORNL)
• Sponsoring Organization: SC USDOE - Office of Science (SC)
• DOE Contract Number: AC05-00OR22725
• OSTI ID: 931761
• Journal Information: Surface Science, Journal Name: Surface Science Journal Issue: 15 Vol. 601; ISSN SUSCAS; ISSN 0039-6028
• Country of Publication: United States
• Language: English

Related Subjects

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
CARBON MONOXIDE
CERIUM OXIDES
CHEMISORPTION
DISSOCIATION
NANOSTRUCTURES
PALLADIUM
RHODIUM
SUBSTRATES