Aluminum anodization in deionized water as electrolyte

Thin oxide films were prepared electrochemically on the aluminum surface using the high-voltage discharge and potentiostatic methods in deionized water as an electrolyte. The growth of continuous films occurred only at potentials lower than the breakdown potential. The films obtained by the discharge method are more uniform and can grow to a higher thickness in comparison to those formed by the potentiostatic mode, as demonstrated by electrochemical impedance spectroscopy (EIS), transmission electron microscopy (TEM), and scanning Kelvin probe force microscopy (SKPFM). The data herein obtained can be used as a reference to understand better the properties of the films produced in conventional electrolytes where apart from water other species are present

Synthesis of ZnO mesoporous powders and their application in dye photodegradation

ZnO materials have attracted considerable interest due to their large - scale potential applications for photodiodes, photocatalysis, sensing and others. For photocatalytical application, ZnO is usually prepared with a mesoporous structure, providing a large surface area for enhancing the system performance. Nowadays, various methods have been explored to prepare ZnO porous powders and films. Among them , the most important and more common techniques to synthetize mesoporous ZnO particles are wet chemical methods , including precipitation from inorganic or organic solution s and sol - gel, owing to their simplicity and low cost. Herein, we studied ZnO mesoporous powder synthesis based on preparation and further thermal decomposition of zinc hydroxide chloride hydrate precursor. The attention was given to the role of reaction medium in the formation of final products and to the photocatalytic activity of the synthesized ZnO.This work has received funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Skło dowska - Curie grant agreement No 645662.publishe

Effect of fluoride-mediated transformations on electrocatalytic performance of thermally treated TiO2 nanotubular layers

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Electrocatalytic activity of Au nanoparticles onto TiO2 nanotubular layers in oxygen electroreduction reaction: size and support effects

Electrocatalytic activity of both bare high-ordered TiO2 nanotubes (TNTs) and gold nanoparticles (Au NPs) loaded TNTs toward oxygen reduction reaction (ORR) has been examined by cyclic voltammetry (CV). Cyclic voltammograms for Au NPs-TNT electrodes are characterized by an additional wave observed at less negative potentials which is responsible for oxygen electroreduction on the surface of gold NPs. The overpotential for O-2 reduction on the Au surface grows with increasing the temperature of TNT annealing and the Au NPs size. The nature of the effects observed was explained by peculiarities of the electron transport through Schottky barrier formed at the Au NPs - TiO2 interface. The width of the Schottky barrier, determined by semiconductor doping level and Au NPs size, plays a key role in the mechanism of electron transport through the space charge region. (C) 2016 Elsevier Ltd. All rights reserved

Electrocatalytic perfomance of nanostructured and compact titania films modified by gold nanoparticles

Основной целью настоящей работы является изучение влияния загрузки наночастиц Au на эффективность наноструктурированных и компактных пленок из диоксида титана

UV-assisted anchoring of gold nanoparticles into TiO2 nanotubes for oxygen electroreduction

Gold nanoparticles (AuNPs) have been deposited on titania nanotubular layers (TNT) via photocatalytic deposition, and the activity of the obtained AuNPs-TNT systems toward oxygen electroreduction reaction (ORR) in an alkaline medium has been studied and compared with the activity of AuNPs TNT composites prepared from Au colloidal solutions. Two photodeposition methods were utilized for anchoring of AuNPs: direct UV-irradiation of a TNT electrode immersed into a HAuCl4 containing solution (TNT-Au1 composites) and initial adsorption of AuCl4− ions on TNT followed by UV irradiation (TNT-Au2 composites). The size, spatial distribution, structure and surface of AuNPs deposited on TNT layers were studied via scanning and transmission electron microscopy, optical spectroscopy and underpotential deposition of lead ad-atoms on gold. It was found that these parameters depend on the photodeposition method. The TNT-Au2 composites have smaller size, higher surface concentration and more uniform distribution of AuNPs in the TNT layers as compared with the TNT-Au1 systems. The electrocatalytic efficiency of Au-TNT electrodes in ORR was found to depend on various factors such as doping level of TNT support (governed by annealing temperature), AuNPs size and their loading amount. The electroreduction of oxygen was observed at less negative potentials when Au nanoparticles were grown on the TNT surface by photoreduction in comparison with the TNT electrodes modified with AuNPs from sols. The enhanced activity of the photocatalytically prepared AuNPs-TNT composites can be explained by the consolidation of the interface between gold nanoparticles and TiO2 support and the absence of ligands on the AuNPs surface.publishe

Photoelectrochemical and Raman characterization of In2O3 mesoporous films sensitized by CdS nanoparticles

The method of successive ion layer adsorption and reaction was applied for the deposition of CdS nanoparticles onto a mesoporous In2O3 substrate. The filling of the nanopores in In2O3 films with CdS particles mainly occurs during the first 30 cycles of the SILAR deposition. The surface modification of In2O3 with CdS nanoparticles leads to the spectral sensitization of photoelectrochemical processes that manifests itself in a red shift of the long-wavelength edge in the photocurrent spectrum by 100–150 nm. Quantum-confinement effects lead to an increase of the bandgap from 2.49 to 2.68 eV when decreasing the number of SILAR cycles from 30 to 10. The spectral shift and the widening of the Raman line belonging to CdS evidences the lattice stress on the CdS/In2O3 interfaces and confirms the formation of a close contact between the nanoparticles

Photocatalytic Deposition of Hydroxyapatite onto a Titanium Dioxide Nanotubular Layer with Fine Tuning of Layer Nanoarchitecture

A new effective method of photocatalytic deposition of hydroxyapatite (HA) onto semiconductor substrates is proposed. A highly ordered nanotubular TiO2 (TNT) layer formed on titanium via its anodization is chosen as the photoactive substrate. The method is based on photodecomposition of the phosphate anion precursor, triethylphosphate (TEP), on the semiconductor surface with the following reaction of formed phosphate anions with calcium cations presented in the solution. HA can be deposited only on irradiated areas, providing the possibility of photoresistfree HA patterning. It is shown that HA deposition can be controlled via pH, light intensity, and duration of the process. Energy-dispersive X-ray spectroscopy profile analysis and glow discharge optical emission spectroscopy of HA-modified TNT prove that HA deposits over the entire TNT depth. High is proven by protein adsorption and pre-osteoblast cell growth

One-step synthesis and growth mechanism of nitrate intercalated ZnAl LDH conversion coatings on zinc

An approach for the synthesis of ZnAl-NO3 LDH conversion coatings on zinc in an aqueous acidic Al(NO3)3/NaNO3 solution is demonstrated for the first time. The growth mechanism has been investigated using time resolved structural, microstructural and analytical methods. A LDH growth model involving both electrochemical and chemical processes is suggested.publishe