Titanium dioxide is a widely used photocatalyst whose properties can be modified by fluoride adsorption. This work is focused on the effect of surface fluorination on the electrochemical and photoelectrocatalytic properties of TiO(2) nanoporous thin films. Surface fluorination was achieved by simple addition of HF to the working solution (pH 3.5). Open circuit potential as well as ex situ XPS measurements verify that surface modification takes place. Fluorination triggers a significant capacitance increase in the accumulation potential region, as revealed by dark voltammetric measurements for all the TiO(2) samples studied. The photoelectrocatalytic properties (measured as photocurrents under white light illumination) depend on the substrate being oxidized and, in some cases, on the nature of the TiO(2) sample. In particular, the results obtained for electrodes prepared with a mixed phase (rutile + anatase) commercial nanopowder (PI-KEM) indicate that the processes mediated by surface trapped holes, such as the photooxidation of water or methanol, are accelerated while those occurring by direct hole capture from the adsorbed state (formic acid) are retarded. The photooxidation of catechol and phenol is also enhanced upon fluorination. In such a case, the effect can be rationalized on the basis of a diminished recombination and a surface displacement of both the oxidizable organic substrates and the poisoning species formed as a result of the organics oxidation. Photoelectrochemical and in situ infrared spectroscopic measurements support these ideas. In a more general vein, the results pave the way toward a better understanding of the photocatalysis phenomena, unravelling the importance of the reactant adsorption processes.
© 2011 American Chemical Society