Photocatalytic Behavior of Fluorinated Rutile TiO₂(110) Surface: Understanding from the Band Model

Surface fluorination of TiO$_2$ (F-TiO$_2$) has complicate photocatalytic behavior in degradation of organic compounds. This work attempts to establish an elegant scenario based on the band model to understand this behavior. Density functional theory (DFT) calculations show that fluorination of the rutile TiO$_2$(110) surface (F-TiO$_2$${110}$) results in the falling of band edges. The falling of valence band edge (VBE) facilitates production of free $\cdot$OH radicals, whereas the falling of conduction band edge (CBE) lowers the reducing power of photo-electrons and inhibits reductive reactions mediated by them. As a result, the photo-electrons are built up in the conduction band which depresses photo-holes in the valence band to produce $\cdot$OH radicals due to the requirement of electrical neutrality and thus leads to a low degradation rate of organic compounds. Even though, our model suggests a route to improve the degradation efficiency, by introducing a scavenger of photo-electrons to promote formation of $\cdot$OH radicals.