화학공학소재연구정보센터
Applied Catalysis B: Environmental, Vol.100, No.1-2, 77-83, 2010
Charge-transfer surface complex of EDTA-TiO2 and its effect on photocatalysis under visible light
We investigated the formation of surface complex between TiO2 and common electron donors (methanol. formic acid, acetic acid, triethanolamine and EDTA) that can absorb visible light through ligand-to-metal charge transfer (LMCT) mechanism. The visible light activity of TiO2-EDTA complex was outstanding among all tested TiO2-substrate complexes. The complexation of EDTA on TiO2 induced a visible light absorption up to 550 nm and exhibited a marked visible light activity for both the reductive conversion of Cr(VI) and the production of H-2. The optimal concentration of EDTA was 100 mu M for the reduction of Cr(VI) but much higher (10 mM) for the production of H-2. The EDTA-adsorbed TiO2 electrode also generated a significant level of photocurrent under visible light irradiation. The LMCT-excited electrons (in TiO2 conduction band) are subsequently transferred to electron acceptors such as Cr(VI) and protons. The degradation of EDTA on TiO2 under visible light was significant only in the presence of Cr(VI) that should scavenge electrons with inhibiting the recombination. The surface CT-complex formation between TiO2 and EDTA was significantly inhibited when the surface of TiO2 was fluorinated. The isoelectric point of TiO2 particles suspended in water was gradually shifted to lower pH values with increasing the concentration of EDTA, which supported the formation of surface complex between TiO2 and EDTA anions. The FT-IR spectra of TiO2-EDTA complex showed a band centered at 1409 cm(-1), which is ascribed to the carboxylate group complexed with TiO2 surface. The complex IR band was diminished upon fluorinating the surface of TiO2. The fact that common electron donors like EDTA can form CT-complexes on the surface of TiO2 and contribute to the visible light activity should be recognized in assessing and understanding the overall photocatalytic activity. (C) 2010 Elsevier B.V. All rights reserved.