Model electrodes with defined mesoscopic structure were either generat
ed by adsorption of surfactant stabilized metal clusters from colloida
l solution on a support of gold or by electrochemical deposition of pl
atinum on gold substrates. Both types of model electrodes were charact
erized by STM (scanning tunnelling microscopy), cyclic voltammetry and
electrooxidation of adsorbed CO. The supported colloidal Pt as well a
s the electrochemically deposited Pt revealed different reactivities r
egarding the CO monolayer electrooxidation as compared to a polycrysta
lline Pt bulk electrode. Tn addition, in-situ FTIR (Fourier transforme
d infrared) spectroscopy was applied to characterize CO adsorbed on el
ectrochemically deposited Pt on gold. Combined with the structural inf
ormation from STM it seems likely that the differences regarding the c
atalytic properties of the model electrodes are due to different cover
ages of the substrate with catalyst particles.