Modeling the noble $metal/TiO2$ (110) interface with hybrid DFT functionals: A periodic electrostatic embedded cluster model study Available to Purchase

The interaction of $Aun$ and $Ptn$ $(n=2,3)$ clusters with the stoichiometric and partially reduced rutile $TiO2$ (110) surfaces has been investigated using periodic slab and periodic electrostatic embedded cluster models. Compared to Au clusters, Pt clusters interact strongly with both stoichiometric and reduced $TiO2$ (110) surfaces and are able to enhance the reducibility of the $TiO2$ (110) surface, i.e., reduce the oxygen vacancy formation energy. The focus of this study is the effect of Hartree–Fock exchange on the description of the strength of chemical bonds at the interface of Au/Pt clusters and the $TiO2$ (110) surface. Hartree–Fock exchange helps describing the changes in the electronic structures due to metal cluster adsorption as well as their effect on the reducibility of the $TiO2$ surface. Finally, the performance of periodic embedded cluster models has been assessed by calculating the Pt adsorption and oxygen vacancy formation energies. Cluster models, together with hybrid PBE0 functional, are able to efficiently compute reasonable electronic structures of the reduced $TiO2$ surface and predict charge localization at surface oxygen vacancies, in agreement with the experimental data, that significantly affect computed adsorption and reaction energies.