The surface interaction between differently prepared tin oxide samples and
CO was studied by Diffuse Reflectance Infrared Fourier Transform (DRIFT)-sp
ectroscopy at room temperature. As samples, commercial powders (Merck) and
home-made powders obtained by a sol-gel preparation were used. Several band
s corresponding to isolated and rooted OH groups, coordinated water and con
densed water in two forms: ordered lavers of water molecules and water in t
he liquid form, were found. Their appearance and intensity depended on the
sample origin and storing conditions. Moreover, the spectra of all samples
show bands corresponding to different hydrated protons (H3O+, H5O2+) and ca
rbonate ions of different intensities. To get information about the interac
tion between SnO2 powders and CO, in-situ measurements were conducted. We f
ound that differently bound water and specific surface OH-groups react with
CO and that surface carbonate ions dissociate because of acidic intermedia
te products. As a result, different bands corresponding to physisorbed CO a
ppear at approximately 2200 cm(-1), together with changes in the region cor
responding to covalent bound chelating and bridging bidentate carbonates an
d carboxylate (between 1700 and 1000 cm(-1)). (C) 2001 Elsevier Science B.V
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