National Institute Of Materials Physics - Romania

Graphene sheets were prepared using electrochemical and chemical steps followed graphite electrochemical oxidation, graphite chemical oxidation, ultrasound expholiation and chemical reduction of carbon material. Films of graphene were electrophoretically deposited from aqueous dispersion on FTO electrode. These films were tested as cathode for a dye-sensitized solar cell. The morphology of the prepared products was imaged by scanning electron microscopy; the intermediate compound, graphene oxide was characterized by IR spectroscopy.

Bismuth-germanate glass ceramics with the composition 40% Bi2O3-60% GeO2 (in molar percents) were prepared through controlled crystallization of melt-quenched glass. The Raman and FTIR spectra recorded in the as-made glasses show broad bands at 240, 400, 780 cm(-1) and 400, 745 cm(-1) have been assigned Ge-O bonds which appear right after preparation. X-ray diffraction has shown that the as-made glasses are amorphous, but after annealing above the crystallization temperature at 558 degrees C, BGO nano-crystallites with a size of about 50 nm precipitate in the glass matrix. The Raman and FTIR spectra reveal sharp peaks associated to the "internal" and "external vibrations" of GeO4 tetrahedral groups inside the BGO nano-crystallites. In the glass ceramic sample the transparency region is shifted at longer wavelengths compared to as-made glass, due to the Rayleigh scattering on the BGO nano-crystallites. (C) 2010 Elsevier B.V. All rights reserved.

The sheltered transfer and immobilization of rabbit anti-human antiserum immunoglobulin G (IgG) by matrix-assisted pulsed laser evaporation (MAPLE) are reported. The iced targets submitted to laser irradiation consisted of 0.2-2 mg/mL IgG blended or not with lipid (L-a-phosphatidylcholine dipalmitoyl) dissolved in distilled water-based saline buffer. Thin IgG coatings were obtained at room temperature onto glass, fused silica, or silicon substrates. Ten thousand subsequent laser pulses of 0.33, 0.5, or 0.67 J/cm(2) fluence were applied for the synthesis of each sample. Morphology and composition of the thin films were studied by optical, scanning, and atomic force microscopy and Fourier transformed infrared spectrometry. Optical labeling methods such as spectrofluorimetry and fluorescence microscopy were selected to verify the biosensor transduction principle because of their high sensitivity for detecting low amounts of antigen (IgG). Protein immobilization to the substrate surface was demonstrated for all obtained structures after immersion in the donkey anti-rabbit secondary antibody solution. The IgG transfer and immobilization onto substrates were improved by addition of lipid to MAPLE solutions. (C) 2010 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 96A: 384-394, 2011.

Free radicals generation is inhibited through green light (GL) irradiation in cellular systems and in chemical reactions. Standard melanocyte cultures were UV-irradiated and the induced cellular reactive oxygen species (ROS) were quantified by the fluorescence technique. The same cell cultures, previously protected by a 24 h GL exposure, displayed a significantly lower ROS production. A simple chemical reaction is subsequently chosen, in which the production of free radicals is well defined. Paraffin wax and mineral oil were GL irradiated during thermal degradation and the oxidation products checked by chemiluminescence [CL] and Fourier transform infrared spectra [FT-IR]. The same clear inhibition of the radical oxidation of alkanes is recorded. A quantum chemistry modeling of these results is performed and a mechanism involving a new type of Rydberg macromolecular systems with implications for biology and medicine is suggested. (C) 2010 Elsevier B.V. All rights reserved.

Surfactant-free emulsion copolymerization was used to prepare methyl methacrylate-hydroxyethyl methacrylate (MMA-HEA) and methyl methacrylate-hydroxypropyl methacrylate (MMA-HPMA) latex particles. Also, glycidyl methacrylate (GMA) was grafted onto the surface of the preformed MMA-HPMA latex particles by seeded surfactant-free emulsion copolymerization. The copolymerization reactions were conducted at 75 A degrees C using a water-soluble initiator, potassium persulfate (KPS). The morphologies of copolymer latex particles were observed using Scanning electron microscopy (SEM). The influence of different reactions parameters (the MMA saturation concentration (Sr), the KPS concentration and the aqueous solubility of the comonomers (HEA or HPMA)) on the particles average diameter and particles size dispersity was investigated. The experimental results showed that the increase of initiator concentration induces in all investigated cases the increase of particles average diameter, while the presence of HEA or HPMA as comonomers in the copolymerization reaction of MMA (1,000% Sr) lead to a decrease of particles average diameter. At small KPS concentration the latex is monodisperse, the increase of the initiator concentration leading to the formation of polydisperse latex. In the case of grafting reaction of GMA onto the monodisperse preformed MMA-HEA latex particles, although the average diameter of the final particles doubles the latex remains quasi-monodisperse.

This work is focused on spectral investigations of Tm3+ doped Sc2O3 transparent ceramic as potential material for diode-pumped solid-state laser emitting around 2 mu m. In the context of the Judd-Ofelt J-O) theory a series of spectroscopic parameters such as J-O intensity parameters, oscillator strengths, radiative transitions probabilities, and radiative lifetimes as well as branching ratios are evaluated. The gain cross-sections which lead to an estimation of the probable operating laser wavelength for the F-3(4) -> H-3(6) Tm3+ laser transition were also calculated. (C) 2010 Elsevier B.V. All rights reserved.

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.