Sol–gel synthesized vanadium doped TiO2 photocatalyst: physicochemical properties and visible light photocatalytic studies

Abstract

Vanadium doped titanium dioxide (V–TiO2) photocatalyst was synthesized by the sol–gel method using ammonium vanadate as vanadium source. The prepared samples were characterized by XRD, N2 adsorption–desorption method, UV–Vis DRS, Fourier transform infrared (FTIR), scanning electron microscope–energy dispersive X-ray and photoluminescence (PL) analysis. The results show that V5+ ions were successfully incorporated into the crystal lattice of TiO2 as a consequence, not only an obvious decrease in the band gap and a red shift of the absorption threshold into the visible light region was recorded for the V modified TiO2, but, also a decrease in photogenerated electrons and holes recombination rate was observed as demonstrated by PL analysis. FTIR study indicated that in undoped TiO2 sample the acetate group favored a bidentate bridging mode of binding with titanium atoms, whereas a bidentate chelating mode of linkage was observed in V–TiO2 powders. The crystallite size of the samples calcined at 300 and 500 °C were decreased beyond the molar ratio of 200:1 (V:Ti), this may be due to dopant presence in the grain boundaries hindering the crystal growth. The photocatalytic activities for both pure and vanadium doped TiO2 powders were tested in the discoloration of a reactive dyestuff, methylene blue, under visible light. The 100:1 (V:Ti) doped photocatalyst, calcined at 300 °C showed enhanced photocatalytic activity under visible light with a rate constant (kobs) of 5.024 × 10−3 min−1 which is nearly five times higher than that of pure TiO2, as result of low band gap value, high specific surface area and a decrease in recombination rate.