Photocatalytic efficiency of titania nonylphenol ethoxylate composite thin films under solar irradiation

Photocatalytic efficiency of titania thin-films on ITO synthesized in the presence of nonylphenol-surfactants containing different numbers of ethoxylate-units was investigated under solar-irradiation. A colorless transparent titania-gel formed in the non-aqueous medium in the presence of nonylphenol-10-ethoxylates while milky white opaque gel was observed with nonylphenol-35-ethoxylates. They were coated on ITO plate by dipping method and calcined at 350, 500 and 700 degrees C. The XRD, IRRAS, EDS, SEM and AFM analyses revealed that different composite nanostructures are formed by calcinations of Ti-nonylphenol-35-ethoxylates at 350 and 500 degrees C. The photocatalytic-efficiencies of the composite films are better than the other titania nanostructures. Transparency and band-gap energy evaluated from transmittance measurements demonstrated that visible-light responsive Ti-nonylphenol-35-ethoxylates composites are more efficient catalysts than UV-absorbable Ti-nonylphenol-b0-ethoxylates films. The photocatalytic degradation rate of the methylene-blue on the catalysts was calculated using the Langmuir-Hinshelwood equation and its modified form derived in this study by considering intensity changes in solar light. The dye degradation efficiency of the Ti-nonylphenol-ethoxylate films changes in the 58-74% range after 2 h of irradiation in 0.02 mM MB solution. The solution completely decolorized after 8 h of irradiation on the TiNP-35 catalysts calcined at 350 degrees C.

Automated summary

The photocatalytic efficiency of titania thin-films on ITO synthesized in the presence of nonylphenol-surfactants containing different numbers of ethoxylate-units was investigated under solar-irradiation. Visible-light responsive Ti-nonylphenol-35-ethoxylates composites are found to be more efficient catalysts than UV-absorbable Ti-nonylphenol-b0-ethoxylates films. The dye degradation efficiency of the Ti-nonylphenol-ethoxylate films changes in the 58-74% range after 2 hours of irradiation in 0.02 mM MB solution, with complete decolorization achieved after 8 hours of irradiation on the TiNP-35 catalysts calcined at 350 degrees C.