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The photocatalytic activity of TiO2 depends on numerous factors, such as the chemical potential of electrons, charge transport properties, band-gap energy, and concentration of surface-active sites. A lot of research has been dedicated to determining the properties that have the most significant influence on the photocatalytic activity of semiconductors. Here, we demonstrated that the activity of TiO2 in the gas-phase reduction of CO2 is governed mainly by the desorption rate of the reaction intermediates and final products. This indicates that the specific surface area of TiO2 and binding strength of reaction intermediates and products are the main factors affecting the photocatalytic activity of TiO2 in the investigated process. Additionally, it was shown that rutile exhibits higher photocatalytic activity than anatase/rutile mixtures mainly due to its high efficiency in the visible portion of the electromagnetic spectrum.

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A series of TiO 2 photocatalysts loaded with various metals (Pt, Pd, Ni, and Cu) were prepared by using the wet impregnation method. Their physicochemical properties were studied by using XRD, BET, TPR-H 2 , FTIR and TPD-NH 3 /CO 2 techniques. The photocatalytic activity of samples was investigated in the gas-phase reduction of carbon dioxide under continuous flow operation mode. Among all investigated catalysts, the Pt and Ni were the most active in terms of the formation rate of methanol. In general, the photocatalytic activity of modified TiO 2 decreased with increasing metal loading and reaction time. The reversible deactivation of photocatalysts was associated with the covering of TiO 2 surface by the reaction products.