National Institute Of Materials Physics - Romania

Amorphous thin films of SnSe2 and Ge2Sb2Te5 doped by different amount of silver (0.1, 0.2, 0.5 and 1 Ag atoms per formula unit) have been prepared by pulsed laser deposition (PLD) starting from solid polycrystalline targets. The films were investigated by X-ray diffraction (XRD), differential scanning calorimetry (DSC), scanning electron microscopy (SEM) and atomic force microscopy (AFM). The good gas sensing properties for CO, as well as the sensitivity for CH4 and NO of the Ag; doped SnSe2 films have been demonstrated in the composition SnSe2Ag0.2. The structural effect of silver introduced in Ge2Sb2Te5 matrix has been investigated. The freshly deposited thin films doped by various amount of Ag develop three phases: an amorphous one, and two crystalline phases consisting of a major fcc cubic phase of AgSbTe2 and a minor cubic phase of composition Ag2Te. (C) 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

Au3Zr intermetallic phase was obtained as pure phase by melt spinning technique. The sample with the same composition obtained by powder metallurgy exhibits some Au4Zr impurity. Rietveld refinements of the X-Ray data were done to obtain the unit cell parameters and atom positions inside the unit cell. Geometry optimizations for the atom positions inside the unit cell were performed by using ab-initio band structure calculations. The calculated values agree well with the ones obtained by Rietveld refinements of the diffraction data. The electronic mechanisms are explained on the basis of the projected densities of states to atom sites.

Intercalation, i.e. the insertion of guest species in a crystalline layered structure, is an efficient route for generating new materials with novel properties. Thin films and crystalline powder of BiI3 layered semiconductor were intercalated by exposure to ammonia vapors at room temperature. The intercalated compound was studied by thermo-gravimetric analysis, differential scanning calorimetry, X-ray diffraction, UV-vis optical absorption, FTIR spectroscopy and Raman scattering. After exposure of BiI3 to ammonia the formation of a new phase, BiI3(NH3)(3.83), was evidenced by thermal analysis. The intercalation process leads to a blue shift of the BiI3 Optical absorption edge by 0.5 eV. The appearance of new Raman lines at 135 and 353 cm(-1) in the Raman spectrum of intercalated BiI3 is considered as an evidence of the chemical interaction between the ammonia molecules and BiI3 lattice. (C) 2009 Elsevier Ltd. All rights reserved.

Calcium phosphate compounds have been studied for biomedical applications due to chemical and structural similarity to the mineral phase of bone and tooth. The composition, physico-chemical properties, crystal size and morphology of synthetic apatite are extremely sensitive to preparative conditions and sometimes it resulted into non-stoichiometric calcium deficient hydroxyapatite (HAp) powders. The present paper refers to calcinations of hydroxyapatite ceramics at 600, 800 and 1000 degrees C. The effect of heat treatment was previously investigated by X-ray diffraction (XRD). The ultrasonic characterisation of hydroxyapatite powders were performed using the ultrasonic air-coupling technique. Modulated ultrasonic signals of 450 kHz central frequency have been transmitted through the hydroxyapatite ceramics specimens. Correlation between signals allowed to draw some conclusions concerning density, attenuation and influence of the preparation temperature influence on these samples. These comparisons and correlation of methods, allow a better characterization of such important materials.

Poly(styrene-hydroxyethyl methacrylate) [P(ST-HEMA)] latex particles were prepared by surfactant-free emulsion copolymerization. As water-soluble initiator was used potassium persulfate (KPS). The influence of different reactions parameters, such as the reaction temperature, the both monomers (ST and HEMA) concentrations and the KPS concentration on the particles average diameter and particles size dispersion was investigated. Generally monodisperse spherical particles are synthesized, but we also obtained stable large three-dimensional colloidal aggregates. These are formed by the agglomeration of monodispersed spheres in certain polymerization conditions. The P(ST-HEMA) monodispersed spheres with 350 nm average diameter were assembled into colloidal crystals using dip-coating technique. Colloidal crystals with different thickness were obtained by modifying two experimental factors, the colloidal concentration and the substrate lifting speed. The morphologies of copolymer latex particles and colloidal crystals were observed using scanning electron microscopy (SEM). The optical properties of colloidal crystals films were also investigated by transmission spectroscopy.

Thin films with nominal composition Fe(78)Si(9)B(13) generated by radio-frequency (rf) sputtering on Si substrates with (100) orientation were irradiated with an eyeliner laser with 130mJ/cm(2) fluence. Information on the induced structural changes were obtained by X-ray diffraction and scanning electron microscopy, while the magnetization curves were determined by the magneto-optical Kerr effect. The effects of the irradiation consist in the growing of crystallites,appearence of melted and ultra-fast frozen zones, surface oxidation and changes in the magnetic properties of the thin films.

Rods of potassium acid phthalate (KAP) and potassium dihydrogen phosphate (KDP) doped with rhodamine 6G (Rh 6G) were grown using the template approach. Pores of hundreds of nanometers in diameter were obtained in polycarbonate (PC) foils after heavy ions irradiation and subsequent chemical etching. Crystallization from solution was used for filling the pores and the nanostructures were characterized using scanning electron microscopy and photoluminescence spectroscopy studies. SEM images of micro- and nano-rods (300 nm and 2.5 mu m diameter) indicate a crystalline growth tendency. When exciting the PC foils containing rods of 100 nm diameter emission bands appear at 581 nm for Rh 6G doped KAP and at 602 nm for Rh 6G doped KDP. A shift of the emission bands towards red was observed when the luminescent properties of the rods with diameters of 100 nm were compared with the luminescent properties of the bulk crystals and of the micrometrical sized rods. (C) 2009 Elsevier Ltd. All rights reserved.

Hybrid systems obtained by incorporation of a nanostructurated material into a matrix from the same thermoelectric (TE) material are predicted to show an increased TE efficiency compared to classical bulk materials. The authors have synthesized Bi1.95Te2.7Se0.35 submicron wires by electrodeposition into a polycarbonate membrane; after polymer membrane dissolution, the wire array supported on a metallic film was electrochemically embedded in a Bi2Te2.65Se0.35 film in order to prepare a hybrid structure. Wires and hybrid structure were analyzed by scanning electron microscopy (SEM), energy X-ray spectrometry (EDX) and X-ray diffraction (XRD).

Oxides glasses are suitable for electronic and optoelectronic applications (band gap higher than 3 eV). Eulytite glasses were obtained from Bi4GeO14 sintered powder or mixture oxides powders Bi2O3-GeO2. The powders rapidly heated and melted at 1050 degrees C for 5 divided by 10 min was poured on the graphite plates under the glass transition temperature. Structural SEM, XRD and EDX investigations were performed at room temperatures. The frequency dependence of the permittivity and loss (45 Hz divided by 5 MHz) was investigated on a large temperature range between -140 and +375 degrees C. The permittivity and loss increase with the temperatures increase and decrease with the frequency increase. An activation energy of 0.88 kcal/mol, comparable to the thermal energy RT = 0.65 kcal/mol, was found for cluster formation on 150 divided by 200 degrees C temperature range. The jump of permittivity on the range 275 divided by 325 degrees C suggest an incipient glass transition at lower temperatures than 400 degrees C, as usually is accepted. The permittivity increase, correlated with the dipolar polarization was noticed at higher temperatures. The decrease of permittivity and loss in 10 divided by 100 kHz frequency range, at the mentioned temperatures, supports this assertion. The estimated relaxation times suggest the big clusters formation. (C) 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

Bi-4(GeO4)(3) glass materials have been characterized by X-ray excited luminescence, photoluminescence and cathodo-luminescence measurements. The materials were obtained by crystallization at different temperatures and their spectroscopic parameters were compared before and after crystallization. Thermoluminescence curves recorded after electron irradiation of BGO glass behave similarly to BGO crystals, showing several peaks between 408 K (135 degrees C) and 610 K (337 degrees C). The differences between the Bi-4(GeO4)(3) crystals and glass materials are believed to result from the random distribution of GeO4 tetrahedra around Bi3+ ions which influences the photoluminescence and TL parameters. The CL images of glass-ceramic samples obtained by partial crystallization at 600 degrees C show luminescent crystalline structures, which are probably responsible for the increase in scintillation efficiency. (C) 2010 Elsevier Ltd. All rights reserved.