Stepan Kment

Notes on the photo-induced characteristics of transition metal-doped and undoped titanium dioxide thin films.

This study reports the preparation of thin nanoparticulate films of titanium dioxide and its modified version doped with a transition metal. The behavior of prepared films was described by means of their photocatalytic and photo-induced electrochemical properties. The TiO(2) and M/TiO(2) (M=Ag, Zr, Fe) thin films were produced via a standard sol-gel method using titanium n-butoxide, acetylacetone, and transition metal acetylacetonates as precursors. Prepared films were analyzed by a series of techniques involving XRD, Raman spectroscopy, SEM, AFM, and XPS. Their photocatalytic activity was monitored with the aid of decomposition of the model compound Rhodamine B in water. All films were then tested for their photo-induced electrochemical properties based on evaluation of polarization curves (photocurrents). The highest reaction rate constant (0.0101min(-1)), which was even higher than that for pure TiO(2), was obtained for the Ag/TiO(2) sample. The highest quantum yield of the charge collection was determined for the undoped TiO(2) film.

TiO2 and Fe2O3 Films for Photoelectrochemical Water Splitting

Titanium oxide (TiO2) and iron oxide (α-Fe2O3) hematite films have potential applications as photoanodes in electrochemical water splitting. In the present work TiO2 and α-Fe2O3 thin films were prepared by two methods, e.g., sol-gel and High Power Impulse Magnetron Sputtering (HiPIMS) and judged on the basis of physical properties such as crystalline structure and surface topography and functional properties such as simulated photoelectrochemical (PEC) water splitting conditions. It was revealed that the HiPIMS method already provides crystalline structures of anatase TiO2 and hematite Fe2O3 during the deposition, whereas to finalize the sol-gel route the as-deposited films must always be annealed to obtain the crystalline phase. Regarding the PEC activity, both TiO2 films show similar photocurrent density, but only when illuminated by UV light. A different situation was observed for hematite films where plasmatic films showed a tenfold enhancement of the stable photocurrent density over the sol-gel hematite films for both UV and visible irradiation. The superior properties of plasmatic films could be explained by ability to address some of the hematite drawbacks by the deposition of very thin films (25 nm) consisting of small densely packed particles and by doping with Sn.

Photoanodes with Fully Controllable Texture: The Enhanced Water Splitting Efficiency of Thin Hematite Films Exhibiting Solely (110) Crystal Orientation.

Hematite, α-Fe2O3, is considered as one of the most promising materials for sustainable hydrogen production via photoelectrochemical water splitting with a theoretical solar-to-hydrogen efficiency of 17%. However, the poor electrical conductivity of hematite is a substantial limitation reducing its efficiency in real experimental conditions. Despite of computing models suggesting that the electrical conductivity is extremely anisotropic, revealing up to 4 orders of magnitude higher electron transport with conduction along the (110) hematite crystal plane, synthetic approaches allowing the sole growth in that direction have not been reported yet. Here, we present a strategy for controlling the crystal orientation of very thin hematite films by adjusting energy of ion flux during advanced pulsed reactive magnetron sputtering technique. The texture and effect of the deposition mode on the film properties were monitored by XRD, conversion electron Mössbauer spectroscopy, XPS, SEM, AFM, PEC water splitting, IPCE, transient photocurrent measurements, and Mott-Schottky analysis. The precise control of the synthetic conditions allowed to fabricate hematite photoanodes exhibiting fully textured structures along (110) and (104) crystal planes with huge differences in photocurrents of 0.65 and 0.02 mA cm(-2) (both at 1.55 V versus RHE), respectively. The photocurrent registered for fully textured (110) film is among record values reported for thin planar films. Moreover, the developed fine-tuning of crystal orientation having a huge impact on the photoefficiency would induce further improvement of thin hematite films mainly if cation doping will be combined with the controllable texture.

Raman spectroscopy of dip-coated and spin-coated sol–gel TiO2 thin films on different types of glass substrate

The photoinduced self-cleaning and super-hydrophilic properties of titania (TiO2) coated glasses are considered to be utilized in many applications. The photocatalytic activity of titania is inherent to the glass composition and to the deposition method. Particularly sodium ions diffused to the titania film from the substrate have tremendous impact on its crystallinity. The deposition method influences surface, structure, and the density of the film. This study aims to provide new findings regarding the mechanism of crystallization of sol–gel synthesized titania and its thin films deposited by means of two different methods (dip-coating and spin-coating) onto the glass substrate with a high content of sodium ions (soda-lime glass) and without sodium ions (quartz glass). The main attention is devoted to Raman spectroscopy and Raman point-to-point mapping of the films. The content and the chemical state of the sodium ions were judged using the XPS. It is shown that the dip-coating method led to dense compact material. In this case the crystallization is localized in randomly distributed centers of nucleation. Contrary the spin-coated samples embodied a web-like pattern of cracks, from which the crystallization proceeds throughout the film. Additionally SEM, AFM, XRD, GDS, UV–VIS methods were performed to support the results.

Ultrathin functional films of titanium(IV) oxide

Chemistry and physics of thin semiconducting layers of various types are subjects of intense research. Especially when nanotechnology methods such as self-assembly are involved, amazing structural and/or functional properties may appear. Also modern physical methods using variously organized plasma arrangements are able to produce uniform structures with distinctive functionality. In this review, based virtually on our own work, discussions on the preparation, structure, morphology, and function of titanium(IV) oxide nanoscopic thin films are presented. It was shown that structurally and functionally similar titanium(IV) oxide films can be prepared via completely different preparation techniques. Function tests were arranged as “primary”, covering the assessment of the light induced charge separation efficiency, and “secondary”, based on photocatalytic surface oxidations.

The Deposition of 3C-SiC Thin Films onto the (111) and (110) Faces of Si Using Pulsed Sputtering of a Hollow Cathode

Thin films of SiC have been deposited using a hollow cathode sputtering technique. Several methods have been used including DC, RF, and pulsed sputtering. The films reported here have been deposited using DC and pulsed sputtering.

Enhanced photocatalytic activity of silver-doped nanoparticulate TiO2 thin films with respect to the method of doping

A nanoparticle photocatalysts based on silver-doped titanium dioxide were synthesized using a modified sol–gel route and also a dip-and-pull step photochemical method. The catalysts were characterized by UV/Vis absorption spectroscopy, atomic force microscopy, X-ray photoelectron spectroscopy, electron microprobe analysis, and Raman spectroscopy. The effects of the experimental parameters on the photoreactivity of the catalysts were evaluated for the decolorization of Rhodamine B in water and by photoelectrochemistry. The activity results show that silver doping significantly promotes the photoreactivity of the titanium dioxide catalyst with some phase transformation from anatase to brookite. The enhanced photoactivity of new nanoparticulate photocatalysts is predominantly attributable to an improvement in crystallinity, band gap lowering, the nature of precursor materials used, and also the method of doping.

Optical emission spectroscopy of High Power Impulse Magnetron Sputtering (HiPIMS) of CIGS thin films

CuIn1-xGaxSe2 (CIGS) thin films with x = 0, 0.28 and 1 were prepared by the sputtering of Cu, In and Ga in HiPIMS (High Power Impulse Magnetron Sputtering) or DC magnetron and subsequently selenized in an Ar+Se atmosphere. Optical emission spectroscopy (OES) was used to monitor differences in HiPIMS and DC plasma during sputtering of metallic precursors. Thin film characteristics were measured using X-ray diffraction (XRD), scanning electron microscopy (SEM), Raman spectroscopy, energy-dispersive X-ray spectroscopy (EDX) and other techniques.

Hematite Photoanode with Complex Nanoarchitecture Providing Tunable Gradient Doping and Low Onset Potential for Photoelectrochemical Water Splitting

Over the past years, α-Fe2 O3 (hematite) has re-emerged as a promising photoanode material in photoelectrochemical (PEC) water splitting. In spite of considerable success in obtaining relatively high solar conversion efficiency, the main drawbacks hindering practical application of hematite are its intrinsically hampered charge transport and sluggish oxygen evolution reaction (OER) kinetics on the photoelectrode surface. In the present work, we report a strategy that synergistically addresses both of these critical limitations. Our approach is based on three key features that are applied simultaneously: i) a careful nanostructuring of the hematite photoanode in the form of nanorods, ii) doping of hematite by Sn4+ ions using a controlled gradient, and iii) surface decoration of hematite by a new class of layered double hydroxide (LDH) OER co-catalysts based on Zn-Co LDH. All three interconnected forms of functionalization result in an extraordinary cathodic shift of the photocurrent onset potential by more than 300 mV and a PEC performance that reaches a photocurrent density of 2.00 mA cm-2 at 1.50 V vs. the reversible hydrogen electrode.

System for time-resolved laser absorption spectroscopy and its application to high-power impulse magnetron sputtering

This paper deals with the development and construction of an apparatus for time-resolved tunable diode laser absorption spectroscopy (LAS) for the diagnostics of pulsed plasma. A detailed description of the extension of a progressive method of laser absorption spectroscopy in continuous regime to a direct triggering method of the time-resolved laser absorption spectroscopy (TR-LAS) is presented. The main advantage of the developed method is its capability to measure the time evolution of the whole absorption profile with a preset time resolution, which can be less than 1 μs. Therefore, the presented method of repetitive sampling applied on LAS in plasma processes is capable of simultaneous measurement of the density and kinetic temperature of selected particles. Its appropriate applications are to periodical processes in technological plasma, namely pulsed plasma discharges. The developed method of TR-LAS was applied to measurements of the temporal evolution of density and kinetic temperature of argon metastable species during high-power impulse magnetron sputtering of titanium and titanium dioxide thin films.