Photodegradation Process of Organic Dyes in the Presence of a Manganese-Doped Zinc Sulfide Nanowire Photocatalyst.

Zinc sulfide (ZnS) nanowires represent a promising candidate in many fields, including optoelectronics and photocatalysis because of their advantages such as excellent optical properties, chemical stability and an easy-scalable simple synthesis method. In this study, an energy-friendly microwave radiation process was used to develop the single-step, solvothermal process for the growth of manganese-doped zinc sulfide (ZnS) and undoped nanocrystals (NCs) in the forms of nanowires using two short amines as a stabilizer, e.g. ethylenediamine and hydrazine, respectively. ZnS nanowires doped with Mn atoms show absorbance in UV and in the visible region of the spectrum. The photocatalytic degradation of rhodamine B in the presence of Mn-doped and undoped ZnS nanocrystals illuminated with only a 6-W UV lamp has been comprehensively studied. The effect of Mn doping and the presence of a nanocrystal stabilizer on the degradation process was determined. It was found that the efficiency of a photocatalytic degradation process was strongly affected by both factors: the doping process of nanowires with Mn2+ atoms and the attachment of ligands to the nanocrystal surface.

Formation and stability of manganese-doped ZnS quantum dot monolayers determined by QCM-D and streaming potential measurements.

Manganese-doped ZnS quantum dots (QDs) stabilized by cysteamine hydrochloride were successfully synthesized. Their thorough physicochemical characteristics were acquired using UV-Vis absorption and photoluminescence spectroscopy, X-ray diffraction, dynamic light scattering (DLS), transmission electron microscopy (HR-TEM), energy dispersive spectroscopy (EDS) and Fourier transform infrared (FT-IR) spectroscopy. The average particle size, derived from HR-TEM, was 3.1nm, which agrees with the hydrodynamic diameter acquired by DLS, that was equal to 3-4nm, depending on ionic strength. The quantum dots also exhibited a large positive zeta potential varying between 75 and 36mV for ionic strength of 10-4 and 10-2M, respectively (at pH 6.2) and an intense luminescent emission at 590nm. The quantum yield was equal to 31% and the optical band gap energy was equal to 4.26eV. The kinetics of QD monolayer formation on silica substrates (silica sensors and oxidized silicon wafers) under convection-controlled transport was quantitatively evaluated by the quartz crystal microbalance (QCM) and the streaming potential measurements. A high stability of the monolayer for ionic strength 10-4 and 10-2M was confirmed in these measurements. The experimental data were adequately reflected by the extended random sequential adsorption model (eRSA). Additionally, thorough electrokinetic characteristics of the QD monolayers and their stability for various ionic strengths and pH were acquired by streaming potential measurements carried out under in situ conditions. These results were quantitatively interpreted in terms of the three-dimensional (3D) electrokinetic model that furnished bulk zeta potential of particles for high ionic strengths that is impractical by other experimental techniques. It is concluded that these results can be used for designing of biosensors of controlled monolayer structure capable to bind various ligands via covalent as well as electrostatic interactions.