@misc{maltanava_synthesis_of_2018, 
author={Maltanava, H., Poznyak, S., Ovodok, E., Ivanovskaya, M., Maia, F., Kudlash, A., Scharnagl, N., Tedim, J.},
title={Synthesis of ZnO mesoporous powders and their application in dye photodegradation},
year={2018},
howpublished = {journal article},
doi = {https://doi.org/10.1016/j.matpr.2018.06.043},
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, Zn5(OH)8Cl2∙H2O or Zn5(OH)8(NO3)2∙(H2O)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 Zn5(OH)8Cl2∙H2O 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.},
note = {Online available at: \url{https://doi.org/10.1016/j.matpr.2018.06.043} (DOI). Maltanava, H.; Poznyak, S.; Ovodok, E.; Ivanovskaya, M.; Maia, F.; Kudlash, A.; Scharnagl, N.; Tedim, J.: Synthesis of ZnO mesoporous powders and their application in dye photodegradation. Materials Today: Proceedings. 2018. vol. 5, no. 9-2, 17414-17421. DOI: 10.1016/j.matpr.2018.06.043}}