The surface chemistry of chromyl chloride (CrO2Cl2) on TiO2(110) was examined with TPD, AES, Delta Phi, measurements, SSIMS, and XPS. CrO2Cl2 adsorbs on TiO2(110) at 130 K with a constant, coverage-independent sticking probability, which is presumably near unity based on TPD. Delta Phi data suggest the molecule is adsorbed with the oxygens bound to the surface and the chlorines pointing into vacuum. In TPD, multilayer CrO2Cl2 desorption occurs at 156 K, and monolayer desorption states occur at about 295 and 430 K. Approximately 0.09 ML. (1 ML = 5.2 x 10(14) sites/cm(2)) desorbs in each of the latter states. The remaining adsorbed CrO2Cl2 (0.48 ML) decomposes irreversibly above 500 K, eventually resulting in CrCl2 desorption above 700 K. No other decomposition products are observed in TPD. Adsorption of CrO2Cl2 at 585 K results in multilayer CrCl2 formation, while adsorption at or below 500 K results in a saturated monolayer. Between 500 and 700 K, XPS results suggest that the Cr deposited from CrO2Cl2 decomposition is reduced, possibly as the result of charge transfer from the defects in the n-doped TiO2(110). SSIMS experiments conducted on the O-18-enriched TiO2(110) indicate that O-16 brought in by CrO2Cl2 is incorporated into the surface, whereas TPD indicates that only a small fraction of this incorporated O-16 is due to isotopic exchange into the desorbing parent at 400 K. Since no oxygen-containing decomposition products were observed in TPD, the decomposition of CrO2Cl2 on TiO2(110) involves reaction at reduced surface sites (oxygen vacancies). As evidence for this, SSIMS indicates that the reaction of O-18(2) With (TiO2)-O-16(110) resulting in O-18 incorporation proceeds above 520 K presumably by the formation of oxygen vacancies from O-16(2) desorption. These results suggest that the reduction and potential immobilization of Cr(VT) species on TiO2 materials may occur thermally if the appropriate surface defect sites are present.