Mesoporous ZnO materials have been synthesized through chemical deposition of different precursors from aqueous or waterethanol solutions followed by their thermal decomposition at 400°C in air. The microstructure and morphology of the precursors and obtained ZnO powders were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscope (TEM) and nitrogen adsorption-desorption (BET) methods. The structure of the precursor and physico-chemical properties of final zinc oxide powders were shown to be considerably influenced by the presence of Clions and ethanol in solution. In water-ethanol solutions, Zn 5 (OH) 8 Cl 2 •H 2 O or Zn 5 (OH) 8 (NO 3 ) 2 •(H 2 O) 2 precursors are formed, while ZnO particles are directly deposited from aqueous solution. The photocatalytic activity of the synthesized ZnO materials was evaluated by the decolorization of Rhodamine B (RhB) upon UV irradiation. The ZnO powders have demonstrated high photocatalytic efficiency, enabling decomposition of 81.497.4 % RhB within 3 hours. The increased photocatalytic efficiency of ZnO prepared by annealing of Zn 5 (OH) 8 Cl 2 •H 2 O precursor or deposited directly from aqueous chloride-containing solutions can be originated from the presence of Cl-containing compounds remaining after thermal treatment of simonkolleite as well as from introduction of Cl-dopant in ZnO.
The composite material filled with nano-sized BaTiO3 and Fe3O4 was designed and studied. The aluminium phosphate ceramics was used as a matrix. The XRD analysis demonstrates only the crystalline structure of the fillers used. The thermogravimetric analysis proves the thermal stability of the composites up to 950 K. The Maxwell–Wagner relaxation was observed in the dielectric spectra of the investigated composites. The dielectric spectroscopy proves the close contact between the nanoparticles with the different ferroic ordering. The phosphate-based composites have been proved to be a prospective candidate for the multiphase multiferroic materials design and development.
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