A method for obtaining nanosized LaCoO3crystals from calcination of a precursor powder synthesized by a hydrothermal route is reported. Details concerning the evolution of the microstructure and formation mechanism of the perovskite phase were studied by powder X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy, Raman spectroscopy, and thermal analysis. It was found that the morphology of the sample progressively turns from a mix of fibers and rods to interconnected nanocrystals. It is determined that LaCoO3phase is produced by a reaction of cobalt and lanthanum oxides, the latter produced by a two-step dehydration process of La(OH)3. Finally, it was found that nearly stoichiometric LaCoO3nanocrystals can be obtained at temperatures as low as 850°C. Nevertheless, whether higher calcination temperatures are used, appropriate reaction times and a controlled atmosphere are required in order to avoid formation of lanthanum carbonates and high density of lattice defects.
In the pulsed laser deposition of thin films, plasma parameters such as energy and density of ions play an important role in the properties of materials. In the present work, cadmium telluride thin films were obtained by laser ablation of a stoichiometric CdTe target in vacuum, using two different values for: substrate temperature (RT and 200 °C) and plasma energy (120 and 200 eV). Structural characterization revealed that the crystalline phase can be changed by controlling both plasma energy and substrate temperature; which affects the corresponding band gap energy. All the thin films showed smooth surfaces and a Te rich composition.
Photocatalytic degradation of methylene blue by graphene decorated titanium dioxide (TiO 2 ) powders heated at different temperatures was analyzed. The powders were prepared by mixing TiO 2 with graphene prepared by the modified Hummers method. A thermal treatment was applied to mixed and pure TiO 2 powders with the aim of analyze their structural dependence on temperature, and consistently their photocatalytic degradation effect on methylene blue solutions exposed to UV and visible radiation. Structural characterization of the powders was carried out by x-ray diffraction and Raman spectroscopy. When irradiated with UV, the mixed powders showed as high as 87% photocatalytic degradation, while the pure TiO 2 reached values of 59%. For visible radiation, as it is expected, the pure TiO 2 showed no activity, while the mixture presented degradation of 40%.
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