Synthesis of ZnO mesoporous powders and their application in dye photodegradation

Abstract Mesoporous ZnO materials have been synthesized through chemical deposition of different precursors from aqueous or water-ethanol 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 Cl – ions 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 81.4-97.4 % 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.