Publications

Thin films of amorphous and polycrystalline indium zinc oxide (IZO) having various In/(In + Zn) nominal compositions from 0.3 to 0.9 were grown by the pulsed laser deposition technique at room temperature or at 400 degrees C on oxidized Si and quartz substrates. After deposition, the films were gamma irradiated at doses of 10, 20 and 30 kGy under Ar atmosphere. Grazing incidence X-ray diffraction investigations could not find measurable changes of the structure after irradiation. Simulations of the X-ray reflectivity (XRR) and diffuse scattering curves acquired from the films showed a small density decrease after irradiation, accompanied by an increase of the thickness and surface roughness. Spectroscopic ellipsometry investigations confirmed the increase of the IZO films' thickness after irradiation, being in agreement with the XRR results. Small changes in the refractive index, most probably caused by changes in the film density were also observed. Four point probe measurements showed very small resistivity increases after irradiation, with the films containing higher In concentration presenting negligible changes. (C) 2016 Elsevier B.V. All rights reserved.

Dye-doped polymer thin films were obtained by spin-coating of 8% polyvinylpyrrolidone (PVP) solutions (in ethanol). Ni or ZnO nanowires were incorporated in Rhodamine 6G doped polymer films (10(-4) M dye concentration). Optical and morphological properties of simple dye-doped polymer films and films containing metallic or semiconducting nanostructures were investigated. Optical microscopy and scanning electron microscopy were used to image the nanowires. The presence of Ni nanowires induces a small shift (2-3 nm) to longer wavelengths on the emission band of Rh 6G doped PVP film. The ZnO nanowires' presence was confirmed by X-ray diffraction measurements. An enhancement of the emission of the dye doped polymer is induced by the semiconducting structures. (C) 2015 Elsevier B.V. All rights reserved.

Hepatocellular carcinoma (HCC) is the most common primary tumor of the liver, ranking as the second most common cause of death from cancer worldwide. Magnetic nanoparticles (MNPs) have been used so far in tumor diagnosis and treatment, demonstrating great potential and promising results. In principle, three different approaches can be used in the treatment of tumors with superparamagnetic iron oxide nanoparticles: magnetically induced hyperthermia, drug targeting and selective suppression of tumor growth. This review focuses on the use of iron oxide nanoparticles for the diagnosis and treatment of liver cancer and offers a walkthrough from the MNPs imaging applicability to further therapeutic options, including their potential flaws. The MNP unique physical and biochemical properties will be mentioned in close relationship to their subsequent effects on the human body, and, also, their toxic potential will be noted. A presentation of what barriers the MNPs should overcome to be more successful will conclude this review.

Our research was focused on the evaluation of the photocatalytic and antimicrobial properties, as well as biocompatibility of cotton fabrics coated with fresh and reused dispersions of nanoscaled TiO2-1% Fe-N particles prepared by the hydrothermal method and post-annealed at 400 degrees C. The powders were characterized by X-ray diffraction (XRD), Mossbauer spectroscopy and X-ray photoelectron spectroscopy. The textiles coated with doped TiO2 were characterized by scanning electron microscopy and energy dispersive X-ray analyses, and their photocatalytic effect by trichromatic coordinates of the materials stained with methylene blue and coffee and exposed to UV, visible and solar light. The resulting doped TiO2 consists of a mixture of prevailing anatase phase and a small amount (similar to 15%-20%) of brookite, containing Fe3+ and nitrogen. By reusing dispersions of TiO2-1% Fe-N, high amounts of photocatalysts were deposited on the fabrics, and the photocatalytic activity was improved, especially under visible light. The treated fabrics exhibited specific antimicrobial features, which were dependent on their composition, microbial strain and incubation time. The in vitro biocompatibility evaluation on CCD-1070Sk dermal fibroblasts confirmed the absence of cytotoxicity after short-term exposure. These results highlight the potential of TiO2-1% Fe-N nanoparticles for further use in the development of innovative self-cleaning and antimicrobial photocatalytic cotton textiles. However, further studies are required in order to assess the long-term skin exposure effects and the possible particle release due to wearing.

The vortex activation energy U-AC in the AC magnetic response of superconductors exhibits a logarithmic variation with the screening current density J (regardless of the pinning structure details), and takes surprisingly high values in the vicinity of the DC irreversibility line, especially at low external DC magnetic fields, as often reported. This is essentially different from the behaviour of the vortex-creep activation energy at long relaxation time scales in DC magnetic measurements, and is not completely understood. We investigated the DC relaxation and the AC response for YBa2Cu3O7 films containing nanorods and nanoparticles, with the DC and AC fields oriented perpendicular to the film surface. It is shown that the large U-AC values in the vicinity of the DC irreversibility line, where the critical-state-related AC signal occurs, are generated by a non-diffusive vortex motion during the AC cycle, with the mean vortex hopping length longer than the average distance between the pinning centres. In these conditions, the smearing of the vortex pinning potential by thermally induced vortex fluctuations is weak, and U-AC mainly results from the strong influence of the pinning-enhanced viscous drag on the vortex hopping process. The logarithmic U-AC(J) dependence is consistent with a high U-AC.

The phenomena occurring at the interface between the electrodes and a liquid with ionic conductivity is manifested specifically in the spectrum of the dielectric permittivity. The theoretical model of the electrode polarization (charge space polarization) is met in the dielectric spectroscopy measurements in which electrodes are conductors (allow transfer of electric charge) and the adsorption-desorption of ions occurs on their surface. A pair of ions with equal and opposite charge is considered. The ions are produced by the association dissociation of neutral molecules. We propope general boundary conditions (BCs) with charge transfer current which contains the adsorption-desorption parameters. The BCs and the basic equations of the Poisson-Nernst Planck model, i.e. transport equations of charge carriers and Poisson equation, are re-formulated through new variables. The mathematical problem is solved analytically. The results allow finding a criterion for choosing a general and simple admittance expression, thus using a unified approach for different cases. We show that the small" signal approximation is no longer needed, at least for modern dielectric spectroscopy equipment. The ions can be point-like or may have finite dimensions. For the last case a model of Stem compact layer with charge transfer is proposed, which allows to calculate the compact layer impedance. Finally we obtain the equivalent admittance of the physical system composed from metal electrodes and ionic liquid in the presence of the Stern layer and the space charge polarization. The limitations of the model are given by the hypothesis of "flat band" and the non-selective adsorption of ions. (C) 2016 Elsevier B.V. All rights reserved.

The growth and thermal stability of textured iridium thin films used as bottom electrode in electronic devices based on ferroelectric materials were investigated. The thin films were grown using the dc magnetron sputtering technique. The Ir layers directly deposited on SiO2/Si substrates present a mixed (111) and (200) orientations, while the films grown on Ti seed layers exhibit a strong preferred (111) orientation favoured by good matching with the titanium lattice. The substrate temperature during the growth of iridium/titanium stack has a significant effect on the surface morphology of the iridium layer and its thermal stability. The as-grown surface of 20-nm-thick Ir films is smooth, having a root-mean-square (rms) roughness of 0.7 nm. After thermal annealing the Ir film shows an increased surface roughness due to the formation of agglomerations. The change in the surface morphology of the Ir layer is due to titanium diffusion and its oxidation. Thicker and better crystallised iridium thin films annealed in oxygen atmosphere at 700 A degrees C show a good thermal stability with only a slight modification of the surface morphology. Within the limits of experimental error, there is no change in the electrical resistivity before and after thermal annealing. The rms roughness has not varied significantly and the XPS investigation shows no traces of titanium oxide on iridium surface. Ir/Ti stack deposited under the optimum conditions could be successfully used as electrode in devices based on oxide thin films.

The inhibitory and antimicrobial effects of silver particles have been known since ancient times. In the last few years, a major health problem has arisen due to pathogenic bacteria resistance to antimicrobial agents. The antibacterial activities of new materials including hydroxyapatite (HAp), silver-doped hydroxyapatite (Ag:HAp) and various types of antibiotics such as tetracycline (T-HAp and T-Ag:HAp) or ciprofloxacin (C-HAp and C-Ag:HAp) have not been studied so far. In this study we reported, for the first time, the preparation and characterization of various thin films based on hydroxyapatite and silver-doped hydroxyapatite combined with tetracycline or ciprofloxacin. The structural and chemical characterization of hydroxyapatite and silver-doped hydroxyapatite thin films has been evaluated by X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). The morphological studies of the HAp, Ag: HAp, T-HAp, T-Ag: HAp, C-HAp and C-Ag: HAp thin solid films were performed using scanning electron microscopy (SEM). In order to study the chemical composition of the coatings, energy dispersive X-ray analysis (EDX) and glow discharge optical emission spectroscopy (GDOES) measurements have been used, obtaining information on the distribution of the elements throughout the film. These studies have confirmed the purity of the prepared hydroxyapatite and silver-doped hydroxyapatite thin films obtained from composite targets containing Ca10-xAgx(PO4)(6)(OH)(2) with x(Ag) = 0 (HAp) and x(Ag) = 0.2 (Ag: HAp). On the other hand, the major aim of this study was the evaluation of the antibacterial activities of ciprofloxacin and tetracycline in the presence of HAp and Ag: HAp thin layers against Staphylococcus aureus and Escherichia coli strains. The antibacterial activities of ciprofloxacin and tetracycline against Staphylococcus aureus and Escherichia coli test strains increased in the presence of HAp and Ag: HAp thin layers.

Density dependent growth and optical properties of periodic arrays of GaAs nanowires (NWs) by fast selective area growth MOVPE are investigated. As the period of the arrays is decreased from 500 nm down to 100 nm, a volume growth enhancement by a factor of up to four compared with the growth of a planar layer is observed. This increase is explained as resulting from increased collection of precursors on the side walls of the nanowires due to the gas flow redistribution in the space between the NWs. Normal spectral reflectance of the arrays is strongly reduced compared with a flat substrate surface in all fabricated arrays. Electromagnetic modeling reveals that this reduction is caused by antireflective action of the nanowire arrays and nanowire-diameter dependent light absorption. Irrespective of the periodicity and diameter, Raman scattering and grazing angle X-ray diffraction show signal from zinc blende and wurtzite phases, the latter-originating from stacking faults, as observed by high resolution transmission electron microscopy. Raman spectra contain intense surface phonons peaks, whose intensity depends strongly on the nanowire diameters as a result of potential structural changes and as well as variations of optical field distribution in the nanowires.