Publications

Lithium borohydride (LiBH4) is a promising material for hydrogen storage, featuring a high gravimetric storage density (above 13 wt. % in the first decomposition step). However, studies of re-hydrogenation of the decomposition products have proven less successful, leading us to the requirement of modified-LiBH4 materials with better absorption-desorption behavior. A Mo-doped mesoporous material was obtained starting from commercial MSU-H and ammonium molybdate. This mesoporous material (MSU-H-type functionalized with molybdenum salt) was used as support in order to impregnate LiBH4. Even though the thermodynamics of LiBH4 hydrogen absorption-desorption is not modified, the desorption kinetics of supported LiBH4 is improved compared to that of pure LiBH4. Moreover, after re-hydrogenation at 450 degrees C only 3.2 wt. % H-2 of storage capacity is recovered for LiBH4, while for supported LiBH4 we achieved almost 5.2 wt. % H-2.

Porous nanoarchitectures based on TiO2 aerogel and colloidal gold particles have been obtained by different synthesis routes: impregnation of TiO2 aerogel with Au colloid, impregnation of TiO2 gel with Au colloid and preparation of TiO2 gel in the presence of Au colloid. The as prepared composites have been thermal treated at 500 degrees C and their structural and morphological properties were investigated. The Raman spectra and XRD data demonstrated the anatase structure of the composite obtained by impregnation of TiO2 aerogel with Au colloid and the mixed anatase-brookite structure of those obtained by impregnation of TiO2 gel with Au colloid and by preparation of TiO2 gel in the presence of Au colloid, respectively. TEM analyses suggest that the Au particles on the TiO2 surface as individual particles, as well as clusters are present. The photocatalytic performances of the synthesized composites were tested in the salicylic acid photodecomposition process and it was found that they are strongly influenced by both anatase - brookite TiO2 structure and Au nanoparticles dispersion on the TiO2 surface.

The to study of the total oxide (SiO2+SiOx) thickness, SiO2 and SiOx (e.g. Si2O, SiO, Si2O3) thicknesses on Si(100) crystalline substrate with take-off angles ranging from 30 degrees to 80 degrees has been carried out by spectrometric method. The d(s) X-ray Photoelectron Spectroscopy (XPS) thicknesses were compared with d(EL) thicknesses obtained by fitting the Spectroscopic Ellipsometry (SE) spectra. A qualitatively good correlation is revealed. However, from these estimations of film thicknesses it results that ellipsometry analysis cannot be as accurate as in XPS evaluation. This is due to uncertainty of used optical constants as well due to very thin oxide films used in this work.

This paper is focused on preparation and microstructure and electrochemical characterization of carbon-TiO2/Pt catalyst used as electrode in fuel cells applications. The platinum deposition was comparatively studied on graphitized carbon substrate and carbon substrate covered with titanium oxide. A strong influence on the platinum deposition, depending of the TiO2 presence, was found. The platinum nanoparticles about 5 nm in size are dispersed in aggregates of 50 to 100 nm on the catalyst surface. This dispersion is strongly affected by the titanium oxide and the substrate porosity. The Pt/TiO2/G and Pt/G electrodes were tested for their catalytic activity in the oxidation of ethanol. The prepared Pt/TiO2/G electrode show higher active surface area than for the Pt/G electrode, this increase in the surface area could be explained to be due to a spreading of wetting or the formation of new active sites at the Pt/oxide interface.

Highly electronegative plasmas were produced in Ar/SF6 gas mixtures in a dc discharge with multipolar magnetic confinement and transversal magnetic filter. Langmuir probe and mass spectrometry were used for plasma diagnostics. Plasma potential drift, the influence of small or large area biased electrodes on plasma parameters, the formation of the negative ion sheath and etching rates by positive and negative ions have been investigated for different experimental conditions. When the electron temperature was reduced below 1 eV the density ratio of negative ion to electron exceeded 100 even for very low amounts of SF6 gas. The plasma potential drift could be controlled by proper wall conditioning. A large electrode biased positively had no effect on plasma potential for density ratios of negative ions to electrons larger than 50. For similar electronegativities or higher a negative ion sheath could be formed by applying a positive bias of a few hundred volts.

We obtain and analyze the effect of electron-electron Coulomb interaction on the time-dependent current flowing through a mesoscopic system connected to biased semi-infinite leads. We assume the contact is gradually switched on in time and we calculate the time-dependent reduced density operator of the sample using the generalized master equation. The many-electron states (MES) of the isolated sample are derived with the exact-diagonalization method. The chemical potentials of the two leads create a bias window which determines which MES are relevant to the charging and discharging of the sample and to the currents, during the transient or steady states. We discuss the contribution of the MES with fixed number of electrons N and we find that in the transient regime there are excited states more active than the ground state even for N=1. This is a dynamical signature of the Coulomb-blockade phenomenon. We discuss numerical results for three sample models: short one-dimensional chain, two-dimensional (2D) lattice, and 2D parabolic quantum wire.

We demonstrate that an anisotropic photonic crystal can modify the shape of a highly convergent incident optical beam. The beam shape engineering is relatively easy, and the photonic crystal is less alignment demanding than beam shapers that incorporate several optical systems. The shape of the output beam can be controlled by an appropriate choice of the angular divergence of the beam, the number of periods and the birefringence values and layer widths of the constituent materials. (C) 2010 Optical Society of America

The optical birefringence of Gd1-xRxCa4O(BO3)(3) (R = Lu or Sc) crystals can be controlled by changing the compositional parameter x. Two nonlinear crystals of Gd0.884Lu0.116Ca4O(BO3)(3) and Gd0.952Sc0.048Ca4O(BO3)(3) with large size and good quality have been grown by Czochralski method. According to our assumptions, the obtained results demonstrate that both crystals convert the near-infrared radiation of 800nm into blue-violet light (400nm) by type-I noncritical phase-matching (NCPM) second-harmonic generation (SHG) processes along Y axis.

Composites prepared from aerosil A380 and liquid crystals (LCs) of 4-n-alkyl-4'-cyanophenyl benzoate type, with four to six carbon atoms in the alkyl chain were investigated by infrared spectroscopy. Their high silica content (of 2-7 g aerosil/1 g of LC) was given by thermogravimetric investigations and allows the observation of a rather thin LC layer on the silica particles. Several surface species onto the external surface of the grains were demonstrated. Arguments are given that monomer and dimer species are present in the bulk cyanophenyl benzoate materials while bulk-like species along with hydrogen-bonded ones coexist in the so-called surface layer of the composites. The main interaction of LC molecules with the aerosil surface is by hydrogen bonding taking place with the involvement of the cyan group. There is a contribution of ester carbonyl group to these surface interactions but this cannot be well quantified. (C) 2009 Elsevier B.V. All rights reserved.

Radiofrequency magnetron sputtering deposition at low temperature (150A degrees C) was used to deposit bioactive glass coatings onto titanium substrates. Three different working atmospheres were used: Ar 100%, Ar + 7%O(2), and Ar + 20%O(2). The preliminary adhesion tests (pull-out) produced excellent adhesion values (similar to 75 MPa) for the as-deposited bio-glass films. Bioactivity tests in simulated body fluid were carried out for 30 days. SEM-EDS, XRD and FTIR measurements were performed. The tests clearly showed strong bioactive features for all the prepared films. The best biomineralization capability, expressed by the thickest chemically grown carbonated hydroxyapatite layer, was obtained for the bio-glass coating sputtered in a reactive atmosphere with 7% O(2).