Abstract
The mechanisms of H2 dissociation on three stoichiometric anatase TiO2 terminations, (001), (100) and (101), have been studied by means of density functional theory (PBE+U) calculations. A two-step process was considered: first, H2 dissociation into H+ and H− pair, and second the H− species migratetion to a neighboring O site, transferring the electrons to the substrate. The (001) termination shows the lowest activation barriers for hydrogen dissociation, 0.37 eV, whereas the highest value was found on (101), 0.98 eV. For hydrogen transfer from Ti to near O, the activation barriers are higher (from 1.10 to 2.37 eV), which indicates the dissociation step is kinetically more favorable than the H transfer process, although the latter is thermodynamically more favorable. Electronic structure, vibrational frequency analysis as well as temperature effects are studied to characterize the reactivity. The relationship between electronic structure, geometry and reactivity is analyzed by means of reactivity descriptors, and the results are compared with ceria and rutile TiO2 facets.
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