In heterogenous catalysis the size of the active metal aggregates is very i
mportant not only because of the large surface-to-bulk ratio of small clust
ers, but also because of the different intrinsic activity of clusters of va
rying size. Using X-ray photoelectron spectroscopy (XPS) and low-energy ion
-scattering spectroscopy (ISS) we investigated the change in size of suppor
ted rhodium clusters on a model catalyst system during temperature treatmen
ts in ultrahigh vacuum. The model catalyst consisted of a thin silicon oxid
e layer, prepared by chemical vapor deposition on a molybdenum substrate, a
nd a nominal load of about two monolayers of rhodium (Rh/SiO2/Mo). During a
nnealing at 773 K, ISS showed an agglomeration of rhodium and an increase o
f the cluster height by a factor of four. The changes in intensity and bind
ing energy of the photoelectron spectra during heating up to 873 K (30 K h(
-1)) can be interpreted with a simple agglomeration model. The three proced
ures allowed a consistent description of the growth of rhodium clusters as
a function of temperature. The influence of vanadium oxide, a catalytic pro
motor material, on the rhodium agglomeraton was studied for a system with t
wo monolayers of vanadium oxide (Rh/VOx/SiO2/Mo). (C) 2000 Elsevier Science
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