ABSTRACT
Commercial rutile TiO2 particles capped with Al2O3 and ZrO2 layers, which are widely used in white pigments, can serve as a starting material for the fabrication of visible light-responsive photocatalysts toward gas-phase NO oxidation. The as-received TiO2 with iron impurities exhibited reduced photocatalytic activity, and the activity was boosted by the deposition of additional iron comparable in quantity to the intrinsic iron impurity level. Analyses using X-ray photoelectron spectroscopy, time-of-flight secondary ion mass spectroscopy, and low-energy ion scattering spectroscopy revealed that the deposited iron and intrinsic impurity iron are dissimilar in terms of location, oxidation states, and interaction with TiO2. This suggests that tracking the structure and impurity levels of photocatalyst elements can be crucial for understanding structure-activity relationships of real catalysts.
