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Evidence for enhanced dissociation of CO on Rh/ceria

Journal Article · · Journal of Catalysis
; ;  [1];  [2]
  1. Univ. of Pennsylvania, Philadelphia, PA (United States). Dept. of Chemical Engineering
  2. Ford Motor Co., Dearborn, MI (United States). Chemical and Physical Sciences Lab.
It is well known that ceria provides oxygen storage capacity (OSC) in three-way automotive catalysts and is important in maintaining oxidation activity during fuel-rich operating conditions. The adsorption and reaction of CO on Rh particles supported on oxidized and partially reduced epitaxial ceria films on yttria-stabilized cubic zirconia (YSZ)(100), (110), and (111) single crystals was studied using temperature-programmed desorption (TPD) and X-ray photoelectron spectroscopy (XPS). The ceria films on YSZ were highly reducible, reacting with CO adsorbed on Rh particles to produce CO{sub 2} during TPD. After reduction of the ceria, however, the CO TPD results contained two features: a low-temperature state resulting from desorption of molecular CO and a high-temperature state resulting from the recombination of C and O atoms produced by CO dissociation at lower temperature. The fraction of CO which dissociated on YSZ-supported Rh/ceria increased with the extent of reduction of the ceria surface. TPD studies with isotopically labeled CO demonstrated that the O atoms produced by CO dissociation undergo exchange with oxygen from the ceria lattice. The CO dissociation reaction was found to be metal specific and was not observed for either Pd or Pt supported on reduced ceria/YSZ.
Sponsoring Organization:
USDOE, Washington, DC (United States)
DOE Contract Number:
FG02-85ER13350; FG02-96ER14682
OSTI ID:
661819
Journal Information:
Journal of Catalysis, Journal Name: Journal of Catalysis Journal Issue: 2 Vol. 178; ISSN 0021-9517; ISSN JCTLA5
Country of Publication:
United States
Language:
English

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