National Institute Of Materials Physics - Romania

We investigated the synthesis of CdS nanoparticles via an optimized water-in-oil microemulsion route that used the non-ionic surfactantbased system H2O-n-octane-Brij30/1-octanol. For that purpose, a microemulsion that contained Cd(II) ions (mu e1) and another microemulsion that contained S2- ions (mu e2) were combined. To investigate the ways in which the non-ionic microemulsion characteristics controlled the size and emission properties of colloidal CdS quantum dots, mu e1 and mu e2 with tunable and robust similar structure were prepared. This requirement was fulfilled by matching the water emulsification failure boundary (wefb) of the two microemulsions and carrying out synthesis along this boundary. Dynamic light scattering and fluorescence probe techniques were used to investigate the size and interfacial organization of the microemulsion water droplets, and the CdS nanoparticles were characterized by UV-Vis and static fluorescence spectrometry, TEM and HRTEM. Nanoparticles of diameter 4.5-5.5 nm exhibiting enhanced band edge emission were produced by increasing the water content of the precursor microemulsions. The experimental results were combined with a Monte Carlo simulation approach to demonstrate that growth via coagulation of seed nuclei represented the driving mechanism for the CdS nanoparticle formation in the water-in-oil microemulsion.

In this paper we report on the stability of CNW layers, synthesized by a radiofrequency plasma jet, against the chemical attack with different acid solutions (sulfuric acid, nitric acid, hydrochloric acid, and hydrofluoric acid). We present the changes of the morphology and structure of the CNW caused by the post-growth chemical treatments. We demonstrate that self-sustaining and transferable CNW layers can be obtained, by chemically dissolving the substrates, while the initial characteristics of the material are well preserved. (C) 2012 Elsevier B.V. All rights reserved.

Nanocrystalline Tm3+(5%)-doped BaTiO3 (BT-Tm) has been synthesized by the sol-gel method. The morphology, structure, and optical properties of powders and ceramics were characterized. The average grain size of the gel precursor annealed at 700 and 900 degrees C was 20 nm and 30 nm, respectively. These powders were single phase and crystallized with a cubic structure while the BT-Tm sintered ceramics were crystallized with the tetragonal BaTiO3 structure. The photoluminescence spectra showed typical transitions of Tm3+ ions and a structure consistent with the Tm3+ ions incorporation in the BaTiO3 crystalline lattice. Thermoluminescence peaks recorded at 300 degrees C (for annealed samples) or at 230 degrees C for the ceramic sample were assigned to the recombination of the Tm2+-electron traps located mainly at the surface of the nano-crystals or inside the microcrystals, respectively. (C) 2012 Elsevier B.V. All rights reserved.

Polarized Raman scattering studies on stiff layered structure of surfactant intercalated with trilayer graphene were performed at different intensities and excitation wavelengths. The D and 2D Raman bands reach the highest and lowest intensity when the polarization of laser excitation light is oriented along and perpendicular on the edges. The 2D band discloses two lorentzian components, separated by similar to 40 cm(-1), which result from the action of interplanar forces, of Casimir nature. The value of similar to 40 cm(-1) is close to the energy value associated with E-2g interplanar layer shear mode evidenced so far only by neutron spectrometry. A new result regards the opposite variation of the intensities of D and 2D bands with the increase of the wavelength of the excitation light. This originates in the different origin of the D and 2D bands; the former is dependent on disorder including also the graphene edges while the latter, results from in a double resonant mechanism combined with a Casimir effect. One demonstrates that the magnitude of Casimir force, which activates interlayer vibration modes, depends on the carrier density on the graphene sheets which can be varied both by the intensity and the wavelength of the excitation laser light. (C) 2012 Elsevier Ltd. All rights reserved.

Buried waveguides have been realized in a 0.7 at.% Nd:YAG single crystal using the direct-writing technique with a femtosecond laser. Efficient laser emission at 1.06 and 1.32 mu m is demonstrated and laser action at 0.94 mu m is obtained using the pump with fiber-coupled diode laser at 807 nm, the first demonstration of such devices.

The high intensity and high repetition rate of the XFEL, the European X-ray Free-Electron Laser presently under construction in Hamburg, results in X-ray doses of up to 1 GGy in silicon sensors for 3 years of operation. Within the AGIPD Collaboration the Hamburg group has systematically studied X-ray-radiation damage using test structures and segmented sensors fabricated on high-ohmic n-type silicon. MOS Capacitors and Gate-Controlled Diodes from 4 vendors with different crystal orientations and different technological parameters, as well as strip sensors have been irradiated in the dose range between 10 kGy and 1 GGy. Current-Voltage, Capacitance/Conductance-Voltage and Thermal Dielectric Relaxation Current measurements were used to extract oxide-charge densities, interface-trap densities and surface-current densities as function of dose and annealing conditions. The results have been implemented into TCAD simulations, and the radiation performance of strip sensors and guard-ring structures simulated and compared to experimental results. Finally, with the help of detailed TCAD simulations, the layout and technological parameters of the AGIPD pixel sensor have been optimized. It is found that the optimization for sensors exposed to high X-ray doses is significantly different than for non-irradiated sensors, and that the specifications of the AGIPD sensor can be met. In 2012 sensors have been ordered, the first batch has been delivered recently, and first results on a comparison between simulations and measurements will be presented.

Recently, vanadium oxide based materials have been intensively studied due to their unique structural, optical, electrical and magnetical properties. In this work, LiZnVO(4)ceramics were obtained by the conventional solid-state reaction method or by the sol-gel technique. We report on the compositional and morphological characterization of LiZnVO4 samples, as well as on the influence of the preparation method on the photoluminescence and dielectric properties. The highest emission intensity was attained for the sol-gel LiZnVO4 powder thermally treated at 600 degrees C, while the best microwave dielectric properties (epsilon(r) similar to 7.5 and Qxf similar to 37900 GHz) were achieved for the conventional LiZnVO4 resonator sintered at 700 degrees C.

The aim of this study was to provide information about the biological properties of iron oxide nanoparticles (IO-NPs) obtained in an aqueous suspension. The IO-NPs were characterized by transmission electron microscopy (TEM). Analysis of hysteresis loops data at room temperature for magnetic IO-NPs sample indicated that the IO-NPs were superparamagnetic at room temperature. The calculated saturation magnetization for magnetic iron oxide was M-s = 18.1 emu/g. The antimicrobial activity of the obtained PMC-NPs was tested against Gram-negative (Pseudomonas aeruginosa 1397, Escherichia coli ATCC 25922), Gram-positive (Enterococcus faecalis ATCC 29212, Bacillus subtilis IC 12488) bacterial as well as fungal (Candida krusei 963) strains. The obtained results suggested that the antimicrobial activity of IO-NPs is dependent on the metallic ions concentrations and on the microbial growth state, either planktonic or adherent. The obtained IO-NPs exhibited no cytotoxic effect on HeLa cells at the active antimicrobial concentrations.

The synthesis of nanosized particles of Ag-doped hydroxyapatite with antibacterial properties is of great interest for the development of new biomedical applications.. e aim of this study was the evaluation of Ca10-xAgx(PO4)(6)(OH)(2) nanoparticles (Ag:HAp-NPs) for their antibacterial and antifungal activity. Resistance to antimicrobial agents by pathogenic bacteria has emerged in the recent years and became a major health problem. Here, we report a method for synthesizing Ag doped nanocrystalline hydroxyapatite. A silver-doped nanocrystalline hydroxyapatite was synthesized at 100 degrees C in deionised water. Also, in this paper Ag:HAp-NPs are evaluated for their antimicrobial activity against ram-positive and ram-negative bacteria and fungal strains. The specific antimicrobial activity revealed by the qualitative assay is demonstrating that our compounds are interacting differently with the microbial targets, probably due to the differences in the microbial wall structures.

Caesalpinia pulcherrima (Linn) popularly known as Peacock flower in India belongs to family Caesalpiniace. In this work, we describe environment friendly technique for green synthesis of gold nanoparticles from AuCl4 solution using the Caesalpinia pulcherrima (Peacock flower) flower extract as reducing agent. The gold nanoparticles were characterized using UV-visible spectroscopy and transmission electron microscopy (TEM). The UV- visible spectra indicate a strong Plasmon resonance that is located at similar to 450 nm. The TEM analysis shows that products have spherical morphology with size ranging between 1.0-50 nm. The study also indicates that gold nanoparticles show good antimicrobial activities when compared to the standard antibiotics.