The catalytic oxidation of CO on Rh foil and small Rh particles suppor
ted by Al2O3 polycrystalline surfaces was studied by the transient exp
eriment of molecular beam surface scattering technique. The supported
Rh particles were prepared by evaporation, using the principle of elec
tron bombardment, The results show the dependence of the CO2 productio
n rate on surface morphology and particle size. The defect rich Rh foi
l surface and smaller particles were found to be more active. The high
oxygen adsorption capacity of 2.5 nm particles as well as their time
dependent form of the CO2 production rate is explained by the oxygen d
iffusion into the subsurface region.