Effects of strong interactions between Ti and ceria on the structures of Ti/CeO2

Abstract

The effects of strong interactions between Ti and ceria on the structures of Ti/CeO₂(111) are systematically investigated by density functional theory calculation. To our best knowledge, the adsorption energy of a Ti atom at the hollow site of CeO₂ is the highest value (−7.99 eV) reported in the literature compared with those of Au (−0.88–−1.26 eV), Ag (−1.42 eV), Cu (−2.69 eV), Pd (−1.75 eV), Pt (−2.62 eV) and Sn (−3.68 eV). It is very interesting to find that Ti adatoms disperse at the hollow site of CeO₂(111) to form surface TiO_x species, instead of aggregating to form Ti metal clusters for the Ti–CeO₂ interactions that are much stronger than those of Ti–Ti ones. Ti adatoms are completely oxidized to Ti⁴⁺ ions if they are monatomically dispersed on the next near hollow sites of CeO₂(111) (xTi-NN-hollow); while Ti³⁺ ions are observed when they locate at the near hollow sites (xTi-N-hollow). Due to the electronic repulsive effects among Ti³⁺ ions, the adsorption energies of xTi-N-hollow are slightly weaker than those of xTi-NN-hollow. Simultaneously, the existence of unstable Ti³⁺ ions on xTi-N-hollow also leads to the restructuring of xTi-N-hollow by surface O atoms of ceria transferring to the top of Ti³⁺ ions, or oxidation by O₂ adsorption and dissociation. Both processes improve the stability of the xTi/CeO₂ system by Ti³⁺ oxidation. Correspondingly, surface TiO₂-like species form. This work sheds light into the structures of metal/CeO₂ catalysts with strong interactions between the metal and the ceria support.