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EN
The modification of titania by metal / non metal ion doping, coupling with narrow band gap sensitizer, surface flourination, metal deposition, and together with recent ventures on application of {001} facets of anatase titania for visible light response with enhanced charge carrier separation are briefly overviewed.
EN
The degradation efficiency of Th-doped TiO2 / TiO2 photocatalysts were investigated under UV and solar light illumination. The model compound chosen for the study was Oryzalin (OZ). Doping of inner transition metal ion Th was intended to modify the electronic properties of TiO2. The Th-doped TiO2 were synthesized by incorporating 0.02, 0.04, 0.06, and 0.1 atom percentage of Th into the TiO2 lattice by solid-state reaction. The stochiometry of the prepared samples is Ti1−xThxO2, where ‘x’ is the percentage of Th. The samples were characterized by UV-Visible absorption, UV-Visible -Diffused reflectance spectra, Scanning Electron Microscopy (SEM), Energy Dispersive X-ray Analysis (EDX) and X-ray Diffraction (XRD). The pore size and surface area of these samples were studied by Brunauer, Emmett and Teller (BET) adsorption method. It was found that metal ion doping at various percentage compositions enables a large shift in the absorption band of the TiO2 towards visible light region. This is due to the formation of various mid band gaps at 2.84 eV, 2.804 eV, 2.66 eV, and 2.55 eV. The extent of degradation of the pesticide was followed by UV-Visible spectroscopy and GC-MS methods. Based on the spectral analysis, the probable degradation reaction mechanism for OZ is proposed. These results indicate that Th-doped TiO2 with the modified electronic properties is a good catalyst under solar light irradiation. But these particles show marginal variation in rates under UV-illumination. All the photodegradation reactions follow the first order kinetics. [...]
EN
Anatase TiO2 was prepared by sol-gel method through the hydrolysis of TiCl4. Ni2+ was doped into the TiO2 matrix in the concentration range of 0.02 to 0.1 at.% and characterized by various analytical techniques. Powder X-ray diffraction revealed only anatase phase for all the samples, while diffuse reflectance spectral studies indicated a red shift in the band gap absorption to the visible region. The photocatalytic activities of these photocatalysts were probed for the degradation of methyl orange under natural solar light. The photocatalyst with optimum doping of 0.08 at.% Ni2+, showed enhanced activity, which is attributed to: (i) effective separation of charge carriers and (ii) large red shift in the band gap to visible region. The influence of crystallite size and dopant concentration on the charge carrier trapping - recombination dynamics is investigated. [...]
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