National Institute Of Materials Physics - Romania

The Bi4Ge3O12 (BGO) glass materials were sintered from a mixture of oxides powders, rapidly heated and melted at 1323 K and poured on the graphite plates heated at different temperatures. Their optical properties are compared with BGO single crystals being strongly dependent by the experimental conditions, which influence the further stability of the samples. The dielectric functions of the samples reveal a clear difference between the two phases (amorphous and crystalline). The refractive index of the amorphous phase has lower values which indicate that the density of the material is diminishes. Also, a sign of disorder is seen in optical absorption (extinction coefficient). From the optical band gap determinations of those two phases, it is confirmed the disorder structure and red-shifts of the band gap value compared with crystalline phase. The absorption spectra are in good agreement with the ellipsometric measurements, regarding the transparency and the edge of the band gap. (C) 2010 Elsevier Masson SAS. All rights reserved.

A new approach for obtaining hybrid inorganic/organic photovoltaic structures, based on CdTe nanowires and organic dye films is reported. The wire arrays of CdTe (10(6) wires/cm(2)) were electrochemically grown using a template method. Ion track polycarbonate foils (30 micrometer thick) were used as templates and the growth conditions for obtaining good quality and stoichiometric CdTe nanowires were identified. After dissolving the polycarbonate template, a CdTe thin film (300 nm) has been deposited by thermal vacuum evaporation onto the wire array before the deposition of ZnPc film as organic absorber. Finally a ZnO thin film was deposited by Electron Pulsed Deposition on ZnPc, working as TCO top electrode. The structural, morphological, electrical and optical properties of each component layer are investigated. Typical parameters of the prepared photovoltaic structures are determined. The external quantum efficiency of the Au/wire array CdTe/CdTe(300 nm)/ZnPc/ZnO structures was significantly increased, with respect to that of Au/wire arrays CdTe/ZnPc/ZnO structures.

Nano-hydroxyapatite bio-ceramics were synthesized by sol-gel method. The gel was dried at 80 degrees C for 96 h. The dried gels were individually heated at a rate of 5 degrees C/min up to 600 degrees C, 800 degrees C, and 1000 degrees C. X-ray diffraction (XRD), transmission electron microscopy (TEM) and scanning electron microscopy (SEM) were used for to characterize the composition, morphology and particle size of samples. At 800 degrees C a small amount of CaO (about 0.3 wt%) was detected in which increased after annealing at 1000 degrees C (about 1.1 wt%). The crystallites are elongated along the c crystallographic axis, but the size anisotropy decreases with increasing temperature above 800 degrees C. The size along the elongation axis increased from 43 nm at 80 degrees C to about 143 nm at 1000 degrees C, as determined by XRD, and from 120 to 280 nm, as measured by TEM. The functional groups were analyzed using Fourier transform infrared (FTIR) and Raman spectroscopies confirming the presence of various and PO43 and OH- bands in the samples. After calcination at 1000 degrees C the bands are more intense which indicates an increase in the cristallynity. The photoluminescence (PL) of HAp treated at various temperatures (80, 600, 800, 1000 degrees C) was also studied. hFOB 1.19 osteoblats cells were used to determine cell proliferation, viability and citotoxicity after interaction with the prepared bioceramics. To evaluate cell proliferation rate quantitative by the hFOB 1.19 cells on HAp samples were cultured to 4 days. Cellular morphology was investigated using FESEM to obtain qualitative information of osteoblast cells on HAp samples. The number of hFOB 1.19 cells on control HAp_80, HAp_600, HAp_800 and HAp_1000 was 400 +/- 30, 360 +/- 25, 350 +/- 21, 320 +/- 16 and 300 +/- 10 after 4 days. Our results proved that the HAp sintered at 1000 degrees C promoted osteoblast cell attachment and adhesion.

The electrodeposition process of Eosin Y/ZnO:Mn as films and nanowires performed using a solution containing zinc and manganese nitrates + lactic acid mixture was studied by linear voltammetry. The films and wires grown by polarization at -1.1 V/SCE electrode potential were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray analysis (EDX), and X-ray photoelectron spectroscopy (XPS). Additionally, the Eosin Y presence was evidenced by optical measurements as absorption and photoluminescence spectroscopy. The manganese content in films depends on the nature of support electrode used. On the other hand, the presence of Eosin Y species in the deposition bath increased significantly the manganese concentration in the ZnO:Mn nanowires electrodeposited at -1.1 V/SCE.

Sucrose is a natural osmolyte accumulated in the cells of organisms as they adapt to environmental stress. In vitro sucrose increases protein stability and forces partially unfolded structures to refold. Thin films of sucrose (C12H22O11) were deposited on thin cut glass substrates by the thermal evaporation technique (P similar to 10(-5) torr). Characteristics of thin films were put into evidence by Fourier Transform Infrared Spectroscopy (FTIR), X-ray Photoelectron Spectroscopy (XPS), scanning electron microscopy (SEM), and differential thermal analysis and thermal gravimetric analysis (TG/DTA). The experimental results confirm a uniform deposition of an adherent layer. In this paper we present a part of the characteristics of sucrose thin films deposited on glass in medium vacuum conditions, as a part of a culture medium for osteoblast cells. Osteoblast cells were used to determine proliferation, viability, and cytotoxicity interactions with sucrose powder and sucrose thin films. The osteoblast cells have been provided from the American Type Culture Collection (ATCC) Centre. The outcome of this study demonstrated the effectiveness of sucrose thin films as a possible nontoxic agent for biomedical applications.

The aim of this paper is the preparation and characterization of hydroxyapatite doped with europium (Eu3+, Eu:Hap). The nanopowders were obtained by coprecipitation method and analyzed through infrared spectroscopy (FT-IR) and Fourier transform Raman spectroscopy (FT-Raman). The preliminary results reveal the nanometric dimension of the particles and indicate that Eu3+ has been introduced into the framework of HAp. The Eu concentration effects of nano Eu: HAp were studied on human osteoblast MG 63 cells in vitro. Our results demonstrate that cell proliferation is not related to the Eu concentration in the HAp particles. This work provides an interesting view of the role of nano Eu: HAp as ideal biomedical materials in future clinical applications.

Europium doped hydroxyapatite (Eu:HAp) nanocristalline powders was synthesized by co-precipitation method by setting the atomic ratio of Eu/[Eu + Ca] at 0% and 2% and [Ca+Eu] /P at 1.67. The structural properties were characterized by X-ray diffraction (XRD). Nitrogen adsorption-desorption isotherms were obtained on different samples using BET method. The X-ray diffraction analysis revealed that hydroxyapatite is the unique crystalline constituent of all the samples, indicating that Eu has been successfully inserted into the HAp lattice. Based on N-2 adsorption-desorption isotherms investigation, the pore size, surface area and pore volume of europium doped hydroxyapatite are 16.57 nm, 115.06 m(2)/g and 0.48 cm(3)/g.

For the first time we presented the preliminary results of biocompatibility studies on bioceramic hydroxyapatite powders doped with europium Ca10-xEux(PO4)(6)(OH)(2), with 0.01 <= x(Eu) <= 0.2 prepared at low temperature by a simple coprecipitation approach. The X-ray diffraction (XRD) studies revealed the characteristic peaks of hydroxyapatite in each sample. No evidence for additional crystalline phases was found, proving the complete substitution of Eu in the HAp lattice in the whole range of concentrations. The scanning electron microscopy (SEM) observations suggest that these materials present a little different morphology, which reveals a homogeneous aspect of the synthesized particles for all samples. The PL investigations shown the PL intensity changed considerably by varying the x(Eu). The value of x(Eu) in the hydroxyapatite formula has almost no effect on the wavelength of emission peaks. In order to test Hap_Eu biocompatibility, the effect of europium substituted hydroxyapatite nanocristalline powders with different x(Eu) on cell viability and proliferation of HEK293 cell line were evaluated. The in vitro investigation showed no significant decrease of viability of HEK293 cell line and low levels of intracellular lipid peroxidation in the Hap_Eu treated cells. In conclusion, the results suggest that Eu doped HAp has low toxicity and exhibit a good biocompatibility.

We report on the development of a modified gas diffusion layer for fuel cells consisting of a simple or teflonized carbon cloth pulsed laser deposited with metal oxide nanostructures designed to operate both as co-catalyst, and oxidic support for other electrochemically active catalysts. We selected TiO2, ZnO and Al2O3 doped (2 wt.%) ZnO which were uniformly distributed over the surface of gas diffusion layers in order to improve the catalytic activity, stability and lifetime, and reduce the production costs of proton exchange membrane fuel cells. We evidenced by scanning electron microscopy and energy dispersive spectroscopy that our depositions consisted of TiO2 nanoparticles while in the case of ZnO and Al2O3 doped (2 wt.%) ZnO transparent quasi-continuous films were synthesized. (C) 2009 Elsevier BM. All rights reserved.

Iron oxide nanoparticles were synthesized in the presence of dextrin. The adsorption process of different dextrin molecules onto the surface of in water dispersed iron-oxide nanoparticles has been investigated to optimize the preparation of iron oxide magnetic fluids. An average iron oxide core size of 8 nm was found by transmission electron microscopy (TEM) for the samples. Scanning electron microscopy (SEM) micro-structural studies revealed a spherical shape of the particles. X-ray phase analysis revealed spinel structure of the iron oxide particles. The attachment of the dextrin on the particle surface was investigated by FTIR spectrometry. The dextrin coated iron oxide nanoparticles were used as targets in Pulsed Laser Deposition (PLD) experiments for thin films synthesis.