National Institute Of Materials Physics - Romania

Ca3-xBaxCo4O9 bulk polycrystalline thermoelectric ceramics with x = 0.00, 0.01, 0.03 and 0.05 have been prepared through a classical solid state method. Microstructural characterizations of sintered samples have shown that Ba has been incorporated into the Ca3Co4O9 and/or Ca3Co2O6 structures and that no Ba-based secondary phases have been produced. The apparent density values increase when the amount of barium is raised with respect to the undoped samples, reaching a maximum value of around 77 % of the Ca3Co4O9 theoretical density, for samples with the highest amount of barium. Electrical resistivity of doped samples decreases in the whole measured temperature range with respect to the undoped ones, while Seebeck coefficient remains practically unchanged. In conclusion, the improvement in resistivity leads to power factor values which are higher than the ones measured in undoped samples, fact which makes this bulk polycrystalline compound a promising candidate for high-temperature power generation applications in oxidative environments.

Hard carbon thin films were synthesized on Si (100) and quartz substrates by the Pulsed Laser Deposition (PLD) technique in vacuum or methane ambient to study their suitability for applications requiring high mechanical resistance. The deposited films' surface morphology was investigated by scanning electron microscopy, crystalline status by X-ray diffraction, packing and density by X-ray reflectivity, chemical bonding by Raman and X-ray photoelectron spectroscopy, adherence by pull-out measurements and mechanical properties by nanoindentation tests. Films synthesized in vacuum were a-C DLC type, while films synthesized in methane were categorized as a-C:H. The majority of PLD films consisted of two layers: one low density layer towards the surface and a higher density layer in contact with the substrate. The deposition gas pressure played a crucial role on films thickness, component layers thickness ratio, structure and mechanical properties. The films were smooth, amorphous and composed of a mixture of sp(3)-sp(2) carbon, with sp(3) content ranging between 50% and 90%. The thickness and density of the two constituent layers of a film directly determined its mechanical properties.

The recovery of the catalysts from the reaction mixture and their recycling is important goals of the current applied catalysis. The stringent ecological and economical demands for sustainability made this concern even more important for the solid catalysts used in the area of biomass catalytic transformations where the raw material usually is not soluble in most of the organic solvents. Therefore, the solid catalyst cannot be easily separated from the mixture of untransformed raw material and by-products (e. g., humines). However, these goals can be achieved by using magnetic nanoparticles (MNPs) based catalysts. This study reports on the magnetic response of two types of new magnetic nanocomposite catalytic systems, Ru@MNP and Nb@AlF3, used in the synthesis of sorbitol/glycerol and of lactic acid, respectively, by direct cellulose degradation. The results showed that the recovering possibilities of the Nb@AlF3 catalysts, with a weaker magnetic response associated to the so called diluted magnetic oxide systems, are much diminished as compared to Ru@MNP, where the magnetic response is generated using MNP supported catalysts. (C) 2015 AIP Publishing LLC.

In this study we aimed to evaluate the biocompatibility and antimicrobial activity of kanamycin functionalized 5 nm-magnetite (Fe3O(4)@ KAN) nanoparticles thin films deposited by Matrix Assisted Pulsed Laser Evaporation (MAPLE) technique. A laser deposition regime was established in order to stoichiometrically transfer Fe3O4@ KAN thin films on silicone and glass substrates. Morphological and physico-chemical properties of powders and coatings were characterized by XRD, TEM, SEM, AFM and IR microscopy(IRM). Our nanostructured thin films have proved efficiency in the prevention of microbial adhesion and mature biofilms development as a result of antibiotic release in its active form. Furthermore, kanamycin functionalized nanostructures exhibit a good biocompatibility, both in vivo and in vitro, demonstrating their potential for implants application. This is the first study reporting the assessment of the in vivo biocompatibility of a magnetite-antimicrobial thin films produced by MAPLE technique. (C) 2014 Elsevier B.V. All rights reserved.

Herein, we investigate the emission properties of Er - BiOCl in the range of similar to 500 to 1700 nm under down - (488 and 973 nm) and NIR (telecom - wavelength at similar to 1500 nm) up - conversion excitation as well high energy X-ray excitation. The dependencies of red (similar to 670 nm) and NIR (similar to 800 nm) to green emission (similar to 543 nm) ratio with Er concentration, excitation mode and delay after laser pulse as well as the up - conversion excitation spectra and decays are analyzed in terms of competitive ground state absorption/excited state absorption and energy transfer up - conversion mechanisms. The CIE chromaticity diagram show single excitation (similar to 1500 nm), delay induced emission color change from yellowish green (delay of 0.001 ms) to reddish orange (delay of 1 ms). The X-ray induced emission of Er - BiOCl presents an atypical red to green emission ratio that exceeds that measured under optical down - conversion excitation by a factor of 13. The potential of Er - BiOCl for optical/X-ray imaging applications is discussed. (C)2015 Optical Society of America

Although a great number of antibiotics are currently available, they are often rendered ineffective by the ability of microbial strains to develop genetic resistance and to grow in biofilms. Since many antimicrobial agents poorly penetrate biofilms, biofilm-associated infections often require high concentrations of antimicrobial agents for effective treatment. Among the various strategies that may be used to inhibit microbial biofilms, one strategy that has generated significant interest involves the use of bioactive surfaces that are resistant to microbial colonization. In this respect, we used matrix assisted pulsed laser evaporation (MAPLE) involving a pulsed KrF* excimer laser source (lambda = 248 nm, tau = 25 ns, nu = 10 Hz) to obtain thin composite biopolymeric films containing natural (flavonoid) or synthetic (antibiotic) compounds as bioactive substances. Chemical composition and film structures were investigated by Fourier transform infrared spectroscopy and X-ray diffraction. Films morphology was studied by scanning electron microscopy and transmission electron microscopy. The antimicrobial assay of the microbial biofilms formed on these films was assessed by the viable cell counts method. The flavonoid-containing thin films showed increased resistance to microbial colonization, highlighting their potential to be used for the design of anti-biofilm surfaces. (C) 2014 Elsevier B.V. All rights reserved.

The inhibiting action of O-ethyl-S-2-(2-hydroxy-3,5-diiodophenyl)-2-oxoethylxantogenate (EHDO) on the oxidation of FeS in air-saturated solutions at pH 1.3 and 25 degrees C was studied using potentiodynamic polarization and electrochemical impedance spectroscopy measurements. The uninhibited and inhibited surfaces were characterized by scanning electron microscopy, energy dispersive X-ray analysis and Raman spectroscopy. It was found that EHDO acts as an anodic inhibitor. Also, it was found that the corrosion of Fe(0) is slower than the oxidative dissolution of uninhibited FeS but faster than the oxidative dissolution of inhibited FeS. This behavior makes EHDO a potential inhibitor of the corrosion of Fe(0) when covered by FeS. (C) 2015 Elsevier B.V. All rights reserved.

This paper presents some studies about the preparation by matrix-assisted pulsed laser evaporation (MAPLE) technique of heterostructures with single layer of arylene based polymer, poly[N-(2-ethylhexy1)2.7-carbazoly1 vinylene]/AMC16 and poly[N-(2-ethylhexy1)2.7-carbazolyl 1.4-phenylene ethynylene]/AMC22, and with layers of these polymers mixed with Buckminsterfullerene/C-60 in the weight ratio of 1:2 (AMC16: C60) and 1:3 (AMC22: C60). The deposited layers have been characterized by spectroscopic (UV-Vis-NIR, PL, FTIR) and microscopic (SEM, AFM) methods. The effect of the polymer particularities on the optical and electrical properties of the structures based on polymer and polymer: C-60 mixed layer has been analyzed. The study of the electrical properties has revealed typical solar cell behavior for the heterostructure prepared by MAPLE on glass/ITO/PEDOT-PSS with AMC16, AMC22 and AMC22: C-60 layer, confirming that this method is adequate for the preparation of polymeric and mixed active layers for solar cells applications. The highest photovoltaic effect was shown by the solar cell structure realized with single layer of AMC16 polymer: g1a55/ITO/PEDOT-PSSIA1VIC16/A1. (C) 2014 Elsevier B.V. All rights reserved.

Magnetic titania nanoparticles covered/embedded in SiO2 shell/matrix were simultaneously manufactured by the single-step laser pyrolysis. The present study is a continuation of our previous investigations on the TiO2/Fe and TiO2/HMDSO (hexamethyldisiloxane) derived-systems. The aim of this work is to study the synthesis by IR (Infrared) laser pyrolysis of magnetic TiO2 based nanocomposites which implies many concurrent processes induced in the gas phase by the laser radiation. The dependence between characteristic properties and the synthesis parameters was determined by many analytical and complementary methods: XRD (X-ray diffraction) structural analysis, UV-vis (ultraviolet-visible) and EDAX (energy-dispersive X-ray) spectroscopy, TEM and HRTEM (transmission electron microscopy at low and high resolution) analysis and magnetic measurements. The results of analysis indicate the presence of disordered silica, Fe, alpha-Fe2O3 and mixtures of anatase and rutile phases with mean crystallite dimensions (in the 14-34 nm range) with typical character of diluted magnetic oxide systems and a lower bandgap energy (E-g = 1.85 eV) as compared with TiO2 P25 Degussa sample. (C) 2014 Elsevier B.V. All rights reserved.

In the present study the formation of lithium cobaltite using a modified Pechini aqueous sol-gel process was investigated. The gelling processes in the lithium-cobalt-citric acid system in 1.1:1:1 molar ratio was performed at 80 A degrees C using aqueous solutions of 0.25 mol/dm(3) of Co(NO3)(2)center dot 6H(2)O with Li(NO3)center dot 6H(2)O or Co(CH3COO)(2)center dot 6H(2)O with Li(CH3COO)center dot 2H(2)O, respectively. The study of the mechanism of gelling of transition metal ion Co(II) in aqueous medium in the presence of lithium ions and citric acid as chelating agents was approached using mainly UV-Vis and FTIR spectroscopic methods. The UV-Vis spectroscopy indicated that the Co(II) ions are in a tetragonal distorted geometry characteristic to a D-4h group symmetry in the solutions in the early steps of the gels formation. After gelling at 80 A degrees C it was observed that the symmetry of the Co(II) ions becomes octahedral (O-h). From the FTIR spectra based on the frequency separation between the antisymmetric stretching nu(as)(COO-) and symmetric stretching nu(sym)(COO-) vibrations, it was identified that the carboxylic groups are bond as a bridging ligands. Using X-ray photoelectron spectroscopy it was identified that the cobalt is present in both final gels as Co(II) ions and the citrate ions are covalently bonded to the cobalt ions. The thermogravimetric/differential thermal analysis showed the thermal stability of the studied gels is higher in the low temperature range for the gels prepared using acetates. Based on the thermal analysis the Li-Co-CA gels were calcinated at 700 A degrees C for 6 h and for each gel a monophasic LiCoO2 was obtained.