Adsorption properties of trifluoroacetic acid on anatase (101) and (001) surfaces: a density functional theory study.

The interaction of trifluoroacetic acid with anatase TiO2(101) and TiO2(001) surfaces has been studied by means of periodic density functional theory based calculations. On the former, the interaction is weak with the adsorbed molecules in a configuration almost indistinguishable from the gas phase structure. On the latter, the interaction is very strong; the molecule adsorbs as trifluoroacetate and releases a proton that binds an oxygen surface atom with a significant distortion of the substrate. The difference in adsorption the mode and strength can be understood from the different structural features of both surfaces and provides arguments to the role of trifluoroacetic as a morphological control agent in the solvothermal synthesis of TiO2 nanoparticles with predominant (001) facets. This, in turn, has a very significant impact on industrial production strategies of value-added TiO2 for photocatalytic applications. Analysis of calculated core level binding energies for F(1s) confirms the experimental assignment to F at the surface as F(-) at Ti surface sites and to F in -CF3 groups of the adsorbed molecule.

Microwave-induced fast crystallization of amorphous hierarchical anatase microspheres.

The fabrication of hierarchical anatase microspheres with potential photocatalytic properties eventually comprises a consolidation step in which a high degree of crystalline order is typically achieved through conventional electric heating treatments. This however entails a substantial reduction in the specific surface area and porosity of the powders, with the consequent deterioration in their photocatalytic response. Here, we have tested the employ of microwave heating as an alternative energy-saving sintering method to promote fast crystallization. The results obtained suggest that under the microwave radiation, the TiO2 hierarchical structures can effectively crystallize in a drastically reduced heating time, allowing the specific surface area and the porosity to be kept in the high values required for an improved photocatalytic performance.

Origin of Optical Excitations in Fluorine-Doped Titania from Response Function Theory: Relevance to Photocatalysis.

We investigate the effect of fluorine doping on the optical spectra of stoichiometric and reduced TiO2 anatase, brookite, and rutile using density functional methods. The present approach is able to reproduce the main features of experiments and high-level quasiparticle calculations for undoped titania but at a much lower computational cost, thus allowing the study of doped titania, which requires large supercells. Whereas the simulated spectra of F-substituted brookite and rutile do not show any significant new feature, a relatively intense new band near the visible region is predicted for F-substituted anatase. This allows one to suggest assigning the spectral features near the visible region, observed on multiphase F-doped titania samples, to the presence of anatase. The physical origin of the new absorption band in F-doped anatase is unambiguously attributed to the presence of Ti(3+) centers.