Ab initio study of the electronic states induced by oxygen vacancies in rutile and anataseTiO2

Abstract

There is an impressive interest in titanium dioxide for its several technological applications which include, e.g., photocatalysis and realization of solar cells. Many of such applications utilize the anatase phase rather than the rutile one, as this appears to be more catalytically active and exhibits a higher electron mobility. In the present study, we address the origin of such differences between the anatase and rutile properties and show that they can be related to a remarkable difference in nature between the electronic levels induced by bulk oxygen vacancies $({V}_{\text{Ox}})$ in the two ${\text{TiO}}_{2}$ polymorphs. These levels have indeed different locations in the energy gap and give rise to different localizations of the electronic charge in real space, thus indicating the ${V}_{\text{Ox}}$'s as important candidates to elucidate the different properties of the two ${\text{TiO}}_{2}$ phases. Present results, achieved by applying a $U$ correction to local spin-density (LSD)--generalized gradient approximation (GGA) methods, stress also the importance of beyond-LSD methods when investigating metal oxides. They show indeed that only such methods permit to reveal the different nature of the ${V}_{\text{Ox}}$ electronic states in the two ${\text{TiO}}_{2}$ phases.