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A Modified Sol-Gel Synthesis of Anatase {001}-TiO 2 /Au Hybrid Nanocomposites for Enhanced Photodegradation of Organic Contaminants.

Abubakar Katsina UsmanDiana-Luciana CursaruGheorghe BrănoiuRaluca ȘomoghiAna-Maria MantaDănuţa MateiSonia Mihai
Published in: Gels (Basel, Switzerland) (2022)
A sol-gel synthesis technique was employed for the preparation of anatase phase {001}-TiO 2 /Au hybrid nanocomposites (NCs). The scalable, schematic, and cost-efficient method was successfully modified using HF and NH 4 OH capping agents. The photocatalytic activity of the as-synthesized {001}-TiO 2 /Au NCs were tested over 2-cycle degradation of methylene blue (MB) dye and pharmaceutical active compounds (PhACs) of ibuprofen and naproxen under direct sunlight illumination at 35 °C and 44,000 lx. Transmission electron microscopy (TEM), high resolution transmission electron microscopy (HR-TEM), fast Fourier transform (FFT), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), energy dispersive X-ray spectroscopy (EDS), and ultraviolet-visible diffuse reflectance spectroscopy (UV-Vis DRS) were employed for the characterization of the as-prepared sample. The characterization results from the TEM, XPS, and XRD studies established both the distribution of Au colloids on the surface of TiO 2 material, and the presence of the highly crystalline structure of anatase {001}-TiO 2 /Au NCs. Photodegradation results from the visible light irradiation of MB indicate an enhanced photocatalytic performance of Au/TiO 2 NCs over TiO 2 . The results from the photocatalytic activity test performed under direct sunlight exposure exhibited promising photodegradation efficiencies. In the first cycle, the sol-gel synthesized material exhibited relatively better efficiencies (91%) with the MB dye and ibuprofen, while the highest degradation efficiency for the second cycle was 79% for the MB dye. Pseudo first-order photodegradation rates from the first cycle were determined to be comparatively slower than those from the second degradation cycle.
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