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The synthesis of a mixed CeO2–ZnO oxide results in a photocatalyst active under visible light. The characterization of the new material shows that Ce does not enter as a dopant in ZnO but rather forms isolated CeO2 nanoparticles supported on the surface of larger particles of the more abundant zinc oxide phase. The as obtained material exhibits a band gap corresponding to UV light (∼3.3 eV), but nevertheless. it shows a relevant photoactivity under irradiation with photons with λ > 420 nm (visible light). The working hypothesis is that visible light irradiation leads to a charge separation and stabilization of a fraction of the carriers connected with the formation of the CeO2/ZnO interface. This phenomenon has been investigated by means of several methods. A specific EPR-based approach allowed to monitor and quantify the charge separation following the formation of holes in the valence band (VB) of the two materials. More complex is detecting the nature of the excited electrons, as this involves the formation of EPR invisible Ce3+ ions by trapping the electrons into localized 4f states of Ce ions at the interface between the two oxides. DFT calculations provide a rational for some of the observed phenomena and a basis for the discussion of the band alignment of the two systems as a consequence of the formation of a heterojunction. The theoretical results show that indeed electrons can be excited at the interface from the VB of the two oxides into the Ce 4f states with photons of 2.3 eV, thus justifying the occurrence of a visible-light activity despite the higher band gap of the two materials.

A combination of electron paramagnetic resonance (EPR) spectra and density functional theory (DFT) calculations is used to characterize the paramagnetic species in rutile N-doped SnO2 samples synthesized by wet chemistry methods. In particular, the nature of paramagnetic N species, substitutional or interstitial, and their effect on the electronic structure are discussed. Complex EPR spectra generated by the interaction of the unpaired electron with N and Sn nuclei have been accurately simulated to obtain the EPR properties (g and A tensors). The results suggest that the N dopants form a rather symmetric structure with three magnetically equivalent or nearly equivalent Sn atoms surrounding the N impurity. After a careful assessment of an all-electron basis set for Sn atoms, realistic models of substitutional and interstitial N-doped SnO2 structures have been designed, and the corresponding hyperfine coupling constants (hpcc) were computed. The comparison between computed and measured hpcc values leads to the assignment of the paramagnetic centers in N-doped SnO2 to substitutional N dopants that take the position of the O atoms in the lattice. The DFT calculations finally suggest the N impurities induce the formation of localized empty states (electron holes) in the intra band gap region.

Recent experiments have indicated that titanium dioxide (TiO(2)) codoped with nitrogen and fluorine may show enhanced photocatalytic activity in the visible region with respect to TiO(2) doped only with nitrogen. Prompted by these findings, we have investigated N-F codoped TiO(2) through a combined theoretical and experimental study. Density functional theory (DFT) calculations have been carried out both within the generalized gradient approximation (GGA) and using hybrid functionals to accurately describe the electronic structure; substitutional as well as interstitial locations of nitrogen in the TiO(2) lattice were considered. From these calculations we infer that N-F codoping reduces the. energy cost of doping and also the amount of defects (number of oxygen vacancies) in the lattice, as a consequence of the charge compensation between the nitrogen (p-dopant) and the fluorine (n-dopant) impurities. The UV-visible spectra of the sol-gel prepared TiO(2) powders confirm the synergistic effect of N-F codoping: more impurities are introduced in the lattice with an increased optical absorption in the visible. EPR spectroscopy measurements on the codoped samples identify two paramagnetic species which are associated to bulk N impurities (N(b)(center dot)) and Ti(3+) ions. Preliminary photocatalytic tests also indicate an enhanced activity under vis-light irradiation toward degradation of methylene blue for the codoped system with respect to N-doped TiO(2).

We report the results of DFT cluster model calculations on the formation of carboxylate radical anions, CO(2)(-), by reaction Of CO(2) with an electron rich MgO surface. The theoretical results are used in conjunction with new pulse electron paramagnetic resonance (EPR) experiments to interpret recently reported experimental data obtained with continuous wave EPR (CW-EPR) (Chiesa, M.; Giamello, E. Chem. Eur. J. 2007, 13, 1261). Three cases have been considered: (1) interaction Of CO(2) with oxide anions at low-coordinated sites and formation of surface carbonates, CO(3)(2-); (2) interaction of CO(2) with ``free{'' electrons trapped at low-coordinated sites of the MgO surface with fort-nation of adsorbed CO(2)(-); and (3) interaction of CO(2) with (H(+))(e(-)) centers and formation of CO(2)(-) species bound near an adsorbed proton (OH group). CO(2) prefers to form surface carbonates and only once most or all the low-coordinated O sites of the surface have reacted it will interact with trapped electrons to form CO(2)(-). Several adsorption sites have been considered, but based on the comparison of measured and computed hyperfine ((13)C and (17)O) and superhyperfine ((1)H) coupling constants we conclude that CO(2)(-) bound at (H(+))(e(-)) centers formed near cationic corners is the most abundant species observed in the experiment.}