Effects of TiO2 Surface Fluorination on Photocatalytic Reactions and Photoelectrochemical Behaviors

Abstract

The formation of surface fluorides on TiO 2 (F−TiO 2 ), which can be easily attained by a simple addition of F - to aqueous TiO 2 suspensions, uniquely affects both photocatalytic reactions and photoelectrochemical behaviors. The fluoride adsorption is favored at acidic pH and greatly reduces the positive surface charge on TiO 2 by replacing ⋮Ti−OH 2 + by ⋮Ti−F species. Effects of surface fluorination on the photocatalytic reactivities are very different depending on the kind of substrates to be degraded. F−TiO 2 is more effective than pure TiO 2 for the photocatalytic oxidation of Acid Orange 7 and phenol, but less effective for the degradation of dichloroacetate. It is proposed that the OH radical mediated oxidation pathways are enhanced on F−TiO 2, whereas the hole transfer mediated oxidations are largely inhibited due to the hindered adsorption (or complexation) of substrates on F−TiO 2 . As for the photocatalytic reduction, the dechlorination of trichloroacetate is much reduced on F−TiO 2 . The photocurrents collected in TiO 2 suspensions, which are mediated by electron shuttles (methyl viologen or ferric ions), and short-circuit photocurrents generated on an illuminated TiO 2 /Ti electrode are also markedly reduced in the presence of F - . The surface ⋮Ti−F group seems to act as an electron-trapping site and to reduce interfacial electron transfer rates by tightly holding trapped electrons due to the strong electronegativity of the fluorine. Finally, elementary charge transfer processes on F−TiO 2 and their implications to photocatalytic reaction pathway are discussed.