Effects of surface fluorination of TiO 2 on the photocatalytic degradation of tetramethylammonium

Abstract

Photocatalytic degradation (PCD) of tetramethylammonium (TMA, (CH 3) 4N +) ions in water was studied using both naked-TiO 2 and fluorinated-TiO 2 (F–TiO 2) in order to investigate how the modification in TiO 2 surface functional groups affects the PCD reaction. A comparison between the naked-TiO 2 and F–TiO 2 systems shows that their relative photoreactivities strongly depend on pH. At pH 3, the addition of fluoride decreases the PCD rate whereas higher degradation rates are obtained at pH 5 and 7 with F–TiO 2. Little fluoride effect on the TMA degradation rate is observed at pH 9. The addition of fluoride affects not only the PCD rate but also the mechanistic pathways of TMA degradation and subsequently the intermediates and product distribution. The modeling result of TiO 2 surface speciation shows that the fluoride addition at pH 3 shifts the dominant surface species from Ti–OH 2 + and Ti–OH to Ti–F (to near completion). This reduces the surface positive charge of TiO 2 (at pH 3) upon adding fluoride and consequently lowers the electrostatic repulsion between the TMA cations and TiO 2 surface. Accordingly, ATR-FTIR spectroscopic measurements show that the TMA concentration at the water/TiO 2 interface is higher on F–TiO 2 than naked-TiO 2 film at pH 3. However, the PCD of TMA on F–TiO 2 at pH 3 is reduced on the contrary, which is ascribed to the depletion of surface OH groups that are the site of surface OH radical formation. At pH 5 and 7, the surface OH sites are not completely diminished even in the presence of fluoride and the presence of surface Ti–F species in fact increases the TMA degradation rate. The fluoride-induced enhancement of PCD is yet to be understood although some speculative arguments are presented.