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Thermo- and photoreactivities of methoxy (CH 3 O(a)) and ethoxy groups (C 2 H 5 O(a)) bonded, via the oxygen atom, to one Ti ion (monodentate adsorption form) or to two Ti ions (bidentate adsorption form) on TiO 2 have been studied by Fourier transformed infrared spectroscopy. Regardless of the similar thermal stability for the two adsorption geometries of the adsorbed alkoxy groups, difference in photoreactivity is observed by monitoring the change of their integrated IR absorptions as a function of UV irradiation time. The monodentate photooxidation rate is ∼1.5 times that of bidentate for both methoxy and ethoxy groups. CH 3 O(a) on TiO 2 is photooxidized to H 2 O(a) and HCOO(a) in the presence of O 2 . On the other hand, C 2 H 5 O(a) is photooxidized to H 2 O(a), HCOO(a), and CH 3 COO(a). A Russell-like mechanism is invoked to explain the formation of the reaction products. Possible reaction steps that control the photoreactivity of the monodentate and bidentate adsorption forms are discussed in terms of this mechanism.
Wu et al. (2000) studied this question.