The adsorption and reaction of CO on Rh particles supported on oxidize
d and partially reduced epitaxial ceria films on yttria-stabilized cub
ic 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, reac
ting with CO adsorbed on Rh particles to produce CO2 during TPD. After
reduction of the ceria, however, the CO TPD results contained two fea
tures: 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 frac
tion of CO which dissociated on YSZ-supported Rh/ceria increased with
the extent of reduction of the ceria surface. TPD studies with isotopi
cally labeled CO demonstrated that the O atoms produced by CO dissocia
tion undergo exchange with oxygen from the ceria lattice. The CO disso
ciation reaction was found to be metal specific and was not observed f
or either Pd or Pt supported on reduced ceria/YSZ. (C) 1998 Academic P
ress.