National Institute Of Materials Physics - Romania

We present the preparation, structural, and magnetic properties of a series of Fe-containing borosilicate glasses as a function of the ratio SiO2/Fe2O3 which is ranging from 1.49 to 2.68. The role of nucleators (Cr2O3 and P2O5) was also investigated. X-Ray diffraction has revealed the formation of magnetite as the major or unique crystalline phase. As SEM micrographs have revealed, the addition of P2O5 give rise to a finer structure as compared with Cr2O3. In addition, the same oxide decreases the temperature of structural transition with almost 100 degrees C. The magnetization data reveal a two step transition at low temperatures: a high temperature transition at T-v = 128 K, which we attribute to the Verwey transition, and a low temperature transition at T-s = 48 K which, most likely, is the result of change in the dynamic of the domain motion.

The influence of Pb2+ doping on the optical properties of LiF crystals before and after irradiation with X-ray was studied by using optical absorption and photoluminescence measurements. After irradiation it was observed an increase of the absorption due to primary and aggregate electronic defects together with a higher photoluminescence signals associated with the F-2 and F-3(+) colour centres in doped samples compared with the undoped ones.

Nanowires made of CdTe were produced by using a template method. Polymer ion track foils (30 micrometers thick) were used as templates, after a proper chemical etching. Nanowires were electrochemically grown in the resulting pores. A discussion of the observed correlations between the morphological/structural properties of the wires and the growth conditions is given. Electrical properties of the arrays of nanowires were studied in the temperature range of 40 K - 300 K, after contacting them by sputtering a gold layer on top of the membranes. Symmetric, non-linear I-V characteristics were recorded in the voltage range used and an activated electrical resistance was observed in the ohmic regime.

Fullerene C-60 has attracted attention due to its special chemical and physical properties. However, its poor solubility and processability arise difficulties in practical applications. These problems may be surpassed by grafting C-60 on polymers. This study presents the synthesis of the polyethylene/maleic anhydride copolymers and C-60 structures and their characterization by photoluminescence. The synthesis of the material is based upon the reaction of fullerene C-60 with amino groups containing in the polymer chains. In the first step, some polyethylene (PE)/maleic anhydride (MA) copolymers having 1, 3, 6 and 10 wt.% anhydride groups were reacted with an amine compound. The following step consists in the reaction of C-60 with the amine groups. A proof that the structures synthesized contain C-60 is given by the photoluminescence spectra.

ZnO is a wide band-gap (ca. 3.4 eV) semiconductor, piezoelectric, pyroelectric, biocompatible, transparent in the visible spectrum and UV light emitting material. The fabrication in 2001 of the first nanobelts of semiconductor oxide materials lead to a rapid expansion of researches concerning one dimensional nanostructures (nanotubes, nanowires, nanobelts), given their possible application in optics, optoelectronics, piezoelectricity, catalysis. Researches carried on up to date evidenced the possibility to obtain an extraordinary variety of ZnO nanostructures, in function of the experimental parameters and the used growth methods. In this work we present morphostructural results on nanostructured ZnO layers obtained by electrochemical deposition. The films have been grown on gold covered glass plates and Si wafers, in various experimental conditions such as: nature of the wetting agents, electrical polarization of the substrate (continuous, pulsed). The influence of the growth conditions on the crystalline structure and morphology of the films is revealed by scanning and transmission electron microscopy studies. The films show a variety of growth morphologies, from entangled-wires-like to honeycomb-like layers. These large-specific-surface layers will be tested as nanostructured substrates for photovoltaic cells with improved efficiency.

Iron- and europium-doped (<= 1 at.%)TiO2 nanoparticles powders have been synthesized by a hydrothermal route at 200 degrees C, starting with TiCl4, FeCl3 center dot 6H(2)O and EuCl3 center dot 6H(2)O. The structure, morphology and optical peculiarities were investigated by means of X-ray diffraction (XRD), transmission electron microscopy (TEM), extended X-ray absorption fine structure (EXAFS), Mossbauer spectroscopy and UV-vis measurements. The photocatalytic performance was analysed in the photodegradation reaction of phenol. Rietveld refinements of XRD patterns reveal that the as-prepared samples consist in iron- and europium-doped TiO2 in the tetragonal anatase structural shape, with particle size as low as 15 nm. By means of Mossbauer spectroscopy on both Fe-57 and Eu-151 isotopes as well as by EXAFS analyses, the presence of Fe3+ and/or Eu3+ ions in the nanosized powders has been evidenced. It was found that iron and europium ions can substitute for titanium in the anatase structure. From the UV-vis reflection spectra, by using the transformed Kubelka-Munk functions, the band gap energy (E-g) of the hydrothermal samples has been determined in comparison with that of Degussa P-25 photocatalyst. A decrease of E-g from 2.9eV found for Degussa photocatalyst to 2.8 eV for the titania doped with 1 at.% Fe has been evidenced, indicating a valuable absorption shift (similar to 20 nm) towards visible light region. However, the best photocatalytic activity in the photodegradation reaction of phenol was evidenced for the hydrothermal sample, TiO2: 1 at.% Fe, 0.5 at.% Eu, in both UV and visible light regions. The photocatalytic activities of iron-doped and iron-europium-codoped samples are high and practically the same only in visible light. The photocatalytic properties in Correlation with the structural and optical peculiarities of the hydrothermal samples are discussed. (C) 2008 Elsevier B.V. All rights reserved.

The effect of fullerene on the radical polymerization of N-vinylpyrrolidone with lauroyl peroxide in toluene was investigated kinetically. C-60 was found to act both as inhibitor and as retarder because the polymerization rate and the molecular weight of resulting poly(vinylpyrrolidone) is decreasing with the increase of the fullerene concentration (0-6.94 x 10(-4) mol l(-1)). The water-soluble poly(vinylpyrrolidone)-modified fullerene C-60 compound was characterized by differential scanning calorimetric, Infrared and Raman spectroscopy, UV absorption and photoluminescence. Based on the results obtained by optical measurements, it is argued that by the covalent attachment of the polymeric radicals to fullerene cage the extended electronic conjugation system of the C-60 is broken leading to the appearance of a polyene structure.

The paper presents the spectroscopic properties of electrolytic colored KCl:Tl and KCI:Tl+Ca crystals and the assignments of the new defects which are formed during electron injection process. The new formed defects Tl-0 and Tl-0+Ca2+ with the metal in the anionic sites, presents very high photoluminescence properties in the near infrared region. Together with those centers, the F-centers, their aggregates and the holes centers are formed during electrolytic coloring process. Their properties were studied by optical absorption (OA), photoluminescence (PL) and thermoluminescence (TL) measurements and compared with those obtained by ionizing irradiation in uncolored KCl:Tl crystals. The results suggest a more efficient Tl+-> Tl-0 process in the case of Ca2+ codoped samples due to the prolonged time of electrons injection, low temperature and high electric field.

The template method was used for preparing Zn1-xCoxO nanowires with x ranging from 0.01 to 0.05. Thus, electrochemical deposition was employed for filling up the pores of polycarbonate ion track nanoporous membranes with the desired material. The method allows a good control over the morphology and composition of the deposited nanowires, as evidenced by scanning electron microscopy (SEM) and energy dispersive X ray analysis (EDX). Measurements of the magnetic properties showed a paramagnetic behavior of the nanowire arrays for the whole set of temperatures and Co concentrations.

We investigated the possibility of tuning luminescent spectra for a given Si/SiO2 nanoparticle size distribution in aqueous solution. The luminescence spectra of Si/SiO2 Suspensions in aqueous solutions of different particle/cluster concentrations were studied. The different Si/SiO2 nanoparticle/cluster concentrations were produced by both centrifugation and dilution. Depending on the centrifugal force we found a reversible shift up to 100 nm toward UV, regardless of the excitation wavelength. The shift could be reverse by sonication of the sample. A-scenario based on particle and cluster size variation is also discussed.