RESUMEN
An Ag-modified TiO2 nanomaterial was prepared by a one-pot synthesis method using tetra butyl titanate, silver nitrate, and sodium hydroxide in water at 473 K for 3 h. X-ray diffraction, scanning electron microscopy, and transmission electron microscopy were used to determine the structure and morphology of the synthesized Ag-modified TiO2 nanomaterial. The diffuse reflectance UV-visible and photoluminescence spectroscopy results revealed that metallic Ag nanoparticles decreased the optical band gap and photoluminescence intensity of the TiO2. In addition, the Raman peak intensity and absorbance were increased after Ag modification onto TiO2. The photocatalytic efficiency of the synthesized samples was tested for decomposition of aqueous hydrazine solution under visible light irradiation. The photocatalytic efficiency of Ag-modified TiO2 nanomaterials was higher than that of bare TiO2 and Ag metal NPs due to the synergistic effect between the Ag metal and TiO2 structures. In addition, the surface plasmon resonance (SPR) electron transfer from Ag metal particles to the conduction band of TiO2 is responsible for superior activity of TiO2-Ag catalyst. The Ag-modified TiO2 nanomaterials offered a 100% H2 selectivity within 30 min of reaction time and an apparent rate constant of 0.018 min-1 with an activation energy of 34.4 kJ/mol under visible light radiation.
RESUMEN
In this study, titanium oxide nanotubes (TiO2NTs) were deposited on the surface of activated carbon (AC) by varying the wt% of AC. The physicochemical properties of synthesized TiO2NTs-AC nanocomposites were analysed by various characterization techniques such as XRD, FT-IR, Raman, DRUV-vis, HR-TEM, XPS, PL, and N2 physisorption. The FT-IR, EDX, and XPS analyses proved the existence of interaction between AC and TiO2NTs. This study found that as the content of AC increases, the surface area and pore volume increase while the energy bandgap decreases. The TiO2NTs-AC nanocomposite with 40% AC exhibited a surface area of 291 m2 g-1, pore volume of 0.045 cm3 g-1 and half pore width = 8.4 Å and had a wide band gap energy (3.15 eV). In addition, the photocatalytic application of the prepared nanocomposites for photocatalytic H2 production was investigated. The H2 was produced via photo-reforming in the presence of a sacrificial agent (methanol) under sunlight irradiation. It was found that the prepared TiO2NTs-AC nanocomposite with 40% AC acted as an efficient photocatalyst for aqueous-methanol reforming under various optimization conditions. Approximately 18 000 µmol-1 hydrogen gas was produced via aqueous-methanol reforming under optimized conditions (catalyst dose = 100 mg, temperature = 25 °C, time = 12 hours, vol. of methanol = 20% (v/v), and pH = 7). The reusability of the TiO2NTs-AC nanocomposite was also investigated for 5 consecutive cycles, and the results suggested only a slight decline in efficiency even after the fifth cycle. This study demonstrates the ability of an activated carbon deposited TiO2NT catalyst to produce hydrogen effectively under sunlight.
RESUMEN
Hydrogen (H2) is a well-known renewable energy source that produces water upon its burning, leaving no harmful emissions. Nanotechnology is utilized to increase hydrogen production using sacrificial reagents. It is an interesting task to develop photocatalysts that are effective, reliable, and affordable for producing H2 from methanol and acetic acid. In the present study, CuO, CdWO4, and CuO-CdWO4 nanocomposite heterostructures were prepared using a cost-efficient, enviro-friendly, and facile green chemistry-based approach. The prepared CuO, CdWO4, and CuO-CdWO4 nanocomposites were characterized using X-ray diffraction pattern, Fourier-transform infrared spectroscopy, diffuse reflectance ultraviolet-visible spectroscopy, scanning electron microscopy, transmission electron microscopy, selected area electron diffraction (SAED) pattern, N2 physisorption, photoluminescence, and X-ray photoelectron spectroscopy techniques. The synthesized photocatalysts were utilized for photocatalytic H2 production using aqueous methanol and acetic acid as the sacrificial reagents under visible light irradiation. The influence of different variables, including visible light irradiation time, catalyst dosage, concentration of sacrificial reagents, and reusability of catalysts, was studied. The maximum H2 was observed while using methanol as a sacrificial agent over CuO-CdWO4 nanocomposite. This enhancement was due to the faster charge separation, higher visible light absorption, and synergistic effect between the CuO-CdWO4 nanocomposite and methanol.