Using ethylene glycol (C2H6O2) as the solvent, ZnS particles were synthesized in high yield at a relatively low temperature of 125 oC via the glycothermal method. We report a facile method for preparing spherical self-aggregated ZnS particles from ZnS nanocrystals, using zinc acetate as the Zn2+ source and thiourea as a sulfur source, without mineralization or other agents. The crystal phase structure, morphology, size, surface chemical composition, and optical properties of the self-aggregated ZnS particles were characterized using XRD, FE-SEM, TEM, XPS, BET, and UV-Vis absorption. The ZnS particles had a cubic phase zinc blende structure without any other impurities. The average crystallite size of the synthesized primary nanocrystal, estimated from XRD peak width and TEM images, was nearly 4 nm. FE-SEM images showed that all of the ZnS consisted of self-aggregated particles with a spherical morphology and a size of approximately 0.2 µm~0.5 µm, and contained many tiny primary nanocrystals. The prepared ZnS exhibited strong photoabsorption in the UV region. The optical band gap decreased from 3.85 eV to 3.62 eV as the glycothermal reaction temperature was increased, due to improvement in particle size and crystallization. The effects of the glycothermal reaction temperature on the photocatalytic activity of the synthesized selfaggregated ZnS particles were investigated by the photodecomposition of methyl orange (MO) dye under UV illumination (λ = 365 nm). The prepared ZnS exhibited excellent photocatalytic degradation with increasing reaction temperature, of 125 oC (5%), 150 oC (10%), 175 oC (60%), and 200 oC (90%) after irradiation for 60 min. It was found that the ZnS particle prepared at 200 oC achieved the highest photocatalytic degradation, with nearly 100% MO decomposition after 90 min, by various photogenerated radical scavengers.
ZnO Nanoparticles with Controllable Ce Content for Efficient Photocatalytic Degradation of MB Synthesized by the Polyol Method
