Marina Ratova

Titanium dioxide thin films were deposited onto sola-lime glass substrates by reactive magnetron sputtering. Fine stainless steel mesh sheets with different aperture sizes were applied as masks over glass substrates to allow the deposition of the coatings with micro-patterned structures and, therefore, enhanced surface area. Non-patterned titania films were deposited for comparison purposes. The titanium dioxide films were post-deposition annealed at 873 K for crystallinity development and then extensively analysed by a number of analytical techniques, including scanning electron microscopy (SEM)/energy-dispersive X-ray spectroscopy (EDX), optical and stylus profilometry, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and UV-Vis spectroscopy. The photocatalytic activity of non-patterned and micro-patterned titania films was assessed under UV light irradiation by three different methods; namely methylene blue, stearic acid, and oleic acid degradation. The results revealed that the micro-patterned coatings significantly outperformed non-patterned titania in all types of photocatalytic tests, due to their higher values of surface area. Increasing the aperture of the stainless steel mesh resulted in lower photocatalytic activity and lower surface area values, compared to the coatings deposited through a smaller aperture mesh.

Bismuth complex oxides, in particular, bismuth tungstate, have recently attracted attention as promising photocatalytic materials for water treatment processes. In the present work, photocatalytic bismuth tungstate films were prepared by pulsed direct current (DC) reactive magnetron sputtering of Bi and W targets in an Ar/O₂ atmosphere onto spherically-shaped glass beads. The uniform coverage of the substrate was enabled by the use of oscillating bowl placed underneath the magnetrons. The atomic ratio of Bi/W was varied through the variation of the power applied to the magnetrons. The deposited coatings were analyzed by the scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), X-ray photoelectron spectroscopy and atomic force microscopy. The photocatalytic properties of the films were studied via the methylene blue (MB) degradation process under artificial (fluorescent light) and natural (sunlight) irradiation, and compared to the photocatalytic performance of titanium dioxide coatings deposited onto identical substrates. The results showed that the photocatalytic performance of bismuth tungstate and bismuth oxide-coated beads was superior to that exhibited by TiO₂-coated beads. Overall, reactive magnetron co-sputtering has been shown to be a promising technique for deposition of narrow band gap bismuth-based semiconducting oxides onto irregularly-shaped substrates for potential use in water treatment applications.

Doping of titanium dioxide with p-block elements is typically described as an efficient pathway for the enhancement of photocatalytic activity. However, the properties of the doped titania films depend greatly on the production method, source of doping, type of substrate, etc. The present work describes the use of pulsed direct current (pDC) magnetron sputtering for the deposition of carbon-doped titania coatings, using CO₂ as the source of carbon; ratios of O₂/CO₂ were varied through variations of CO₂ flow rates and oxygen flow control setpoints. Additionally, undoped Titanium dioxide (TiO₂) coatings were prepared under identical deposition conditions for comparison purposes. Coatings were post-deposition annealed at 873 K and analysed with scanning electron microscopy (SEM), X-ray diffreaction (XRD), atomic force microscopy (AFM), and X-ray photoelectron spectroscopy (XPS). The photocatalytic properties of the thin films were evaluated under ultraviolet (UV) and visible light irradiation using methylene blue and stearic acid decomposition tests. Photoinduced hydrophilicity was assessed through measurements of the water contact angle under UV and visible light irradiation. It was found that, though C-doping resulted in improved dye degradation compared to undoped TiO₂, the UV-induced photoactivity of Carbon-doped (C-doped) photocatalysts was lower for both model pollutants used.

Atmospheric pressure plasma treatment of the surface of a polypropylene film can significantly increase its surface energy and, thereby improve the printability of the film. A laboratory-scale dielectric barrier discharge (DBD) system has therefore been developed, which simulates the electrode configuration and reel-to-reel web transport mechanism used in a typical industrial-scale system. By treating the polypropylene in a nitrogen discharge, we have shown that the water contact angle could be reduced by as much as 40° compared to the untreated film, corresponding to an increase in surface energy of 14 mNm⁻¹. Ink pull-off tests showed that the DBD plasma treatment resulted in excellent adhesion of solvent-based inks to the polypropylene film.

A novel powder handling technique was used to allow the deposition of bismuth tungstate coatings onto commercial titanium dioxide photocatalytic nanoparticles. The coatings were deposited by reactive pulsed DC magnetron sputtering in an argon/oxygen atmosphere. The use of an oscillating bowl with rotary particle propagation, positioned beneath two closed-field planar magnetrons, provided uniform coverage of the titania particle surfaces. The bismuth/tungsten atomic ratio of the coatings was controlled by varying the power applied to each target. The resulting materials were characterized by X-ray diffraction, energy-dispersive X-ray spectroscopy (EDX), Brunauer–Emmett–Teller (BET) surface area measurements, transmission electron microscopy (TEM), and UV-visible diffuse reflectance spectroscopy. Photocatalytic properties under visible light irradiation were assessed using an acetone degradation test. It was found that deposition of bismuth tungstate onto titania nanoparticles resulted in significant increases in visible light photocatalytic activity, compared to uncoated titania. Of the coatings studied, the highest photocatalytic activity was measured for the sample with a Bi/W atomic ratio of 2/1.

Bismuth molybdate thin films were deposited by reactive magnetron co-sputtering from two metallic targets in an argon/oxygen atmosphere, reportedly for the first time. Energy dispersive X-ray spectroscopy (EDX) analysis showed that the ratio of bismuth to molybdenum in the coatings can be effectively controlled by varying the power applied to each target. Deposited coatings were annealed in air at 673 K for 30 min. The crystalline structure was assessed by means of Raman spectroscopy and X-ray diffraction (XRD). Oxidation state information was obtained by X-ray photoelectron spectroscopy (XPS). Photodegradation of organic dyes methylene blue and rhodamine B was used for evaluation of the photocatalytic properties of the coatings under a visible light source. The photocatalytic properties of the deposited coatings were then compared to a sample of commercial titanium dioxide-based photocatalytic product. The repeatability of the dye degradation reactions and photocatalytic coating reusability are discussed. It was found that coatings with a Bi:Mo ratio of approximately 2:1 exhibited the highest photocatalytic activity of the coatings studied; its efficacy in dye photodegradation significantly outperformed a sample of commercial photocatalytic coating.