National Institute Of Materials Physics - Romania

A general method for mapping the equipotential profile surrounding a conductive cylindrically symmetric high aspect ratio structure, such as a carbon nanotube or a Spindt tip, is devised. The surface of the object is replaced by a discrete set of charges located on the symmetry axis. The overall electrostatic potential must satisfy a set of boundary conditions imposed on the original surface. The optimum number of charges is determined through an iterative self-validating process such that the obtained equipotential mimics the surface of the object. The method is exemplified by calculating the electric field enhancement factor for rounded cones and cylinders resembling Spindt tips and carbon nanotubes, respectively. (C) 2011 American Institute of Physics. [doi: 10.1063/1.3582141]

This paper discusses two arylenevinylene oligomers with optical nonlinear properties. Their trans molecular structure was confirmed by Fourier Transform Infrared Spectroscopy and Nuclear Magnetic Resonance. Second Harmonic Generation and two-photon fluorescence have been observed on Matrix Assisted Pulsed Laser Evaporation-deposited thin films. We have seen two local maxima in UV-Vis spectra and a red shift of the photoluminescence peak for carbazole-based oligomer, which can be correlated with a higher conformational flexibility and with strong polarization interactions in the solid state. Scanning Electron Microscopy and Atomic Force Microscopy images have revealed a grainy morphology of the film deposited on titanium and a higher roughness for carbazole-based oligomer. Second harmonic measurements have shown nearly equal values of the second-order nonlinear optical coefficient for the triphenylamine and carbazole-based oligomers for P-laser < 100 mW. z-Scan and x-scan representations of the carbazole-based oligomer film have shown strong two-photon fluorescence intensity inside the sample confirming a volume process, and a strong second harmonic at the surface of the sample determined by the surface morphology. (C) 2010 Elsevier B.V. All rights reserved.

Iron/iron carbide core and carbon shell nanoparticles with improved magnetic properties were successfully synthesized by laser pyrolysis. As iron and carbon precursors, iron pentacarbonyl and pure or argon-diluted acetylene/ethylene mixtures, respectively, were used. The aim of the present optimization is the improvement of the magnetic properties of the nanomaterials by the increase of the iron percent in powders simultaneously to the maintaining of the protective character of the carbon coverage of nanoparticles. The chemical content and the crystalline structure were monitored by EDX, XRD and TEM techniques. In the first study, the content of acetylene as carbon source was diminished from 75% to 0%. Consequently the percent iron increased from 10 at.% to 28 at.% while oxygen remained relatively constant (around 5 at.%). In the second step, only diluted ethylene was used (maximum 87.5 vol.% Ar). In this case, an increase of iron to 46 at.% is observed. An optimum 50% carbon source dilution was found. Above this value, the carbon content increases and below it, superficial oxidation increases through the diminishing of the carbon shell. The magnetic properties and the Fe phase composition of the Fe-C samples were analyzed by temperature dependent Mossbauer spectroscopy. (C) 2010 Elsevier B.V. All rights reserved.

Complex oxides demonstrate specific electric and magnetic properties which make them suitable for a wide variety of applications, including dilute magnetic semiconductors for spin electronics. A tin-iron oxide Sn(1-x)FexO(2) nanoparticulate material has been successfully synthesized by using the laser pyrolysis of tetramethyl tin-iron pentacarbonyl-air mixtures. Fe doping of SnO2 nanoparticles has been varied systematically in the 3-10 at% range. As determined by EDAX, the Fe/Sn ratio (in at%) in powders varied between 0.14 and 0.64. XRD studies of Sn(1-x)FexO(2) nanoscale powders, revealed only structurally modified SnO2 due to the incorporation of Fe into the lattice mainly by substitutional changes. The substitution of Fe3+ in the Sn4+ positions (Fe3+ has smaller ionic radius as compared to the ionic radius of 0.69 angstrom for Sn4+) with the formation of a mixed oxide Sn1-xFexO(2) is suggested. A lattice contraction consistent with the determined Fe/Sn atomic ratios was observed. The nanoparticle size decreases with the Fe doping (about 7 nm for the highest Fe content). Temperature dependent 57Fe Mossbauer spectroscopy data point to the additional presence of defected Fe3+-based oxide nanoclusters with blocking temperatures below 60 K. A new Fe phase presenting magnetic order at substantially higher temperatures was evidenced and assigned to a new type of magnetism relating to the dispersed Fe ions into the SnO2 matrix. (C) 2010 Elsevier B.V. All rights reserved.

This review deals with recent progress on the development of composite materials based on cojugated polymers (CPs) and carbon nanotubes (CNTs), both from fundamental and applied point of view. In the first part of the manuscript, we present the different types of composites, the new protocols used in their synthesis as well as their vibrational properties reported in the last five years. A brief review of the contribution of Raman light scattering and FTIR spectroscopy to establish the type of interaction between the two constituents is discussed for different cases, i.e. bi-layers of polymers and carbon nanotubes, CPs doped with CNTs and CNTs functionalized with CPs. Recently, anti-Stokes resonant Raman studies have appeared as fruithful tools in the evaluation of functionalization process of CNTs with CPs. The review provides also information on CPs/CNTs composite properties specific to applications in the field of energy storage, optical limiting and electron field emission devices, transistors, conducting textiles, sensors, rewritable devices, biomedical and food domains as well as how these materials have been optimized to generate exploitable properties.

Indium oxide-doped hematite xIn(2)O(3)center dot(1 - x)alpha-Fe2O3 (x = 0.1-0.7) nanostructure system was synthesized using mechanochemical activation by ball milling and characterized by XRD, simultaneous DSC-TGA, and UV/Vis/NIR. The microstructure and thermal behavior of as obtained system were dependent on the starting In2O3 molar concentration x and ball milling time. XRD patterns yielded the dependence of lattice parameters and grain size as a function of ball milling time. After 12 h of ball milling, the completion of In3+ substitution of Fe3+ in hematite lattice occurs for x = 0.1, indicating that the solid solubility of In2O3 in hematite lattice is extended. For x = 0.3, 0.5, and 0.7, the substitutions between In3+ and Fe3+ into hematite and In2O3 lattice occur simultaneously. The lattice parameters a and c of hematite and lattice parameter a of indium oxide vary as a function of ball milling time. The changes of these parameters are due to ion substitutions between In3+ and Fe3+ and the decrease in the grain sizes. Ball milling has a strong effect on the thermal behavior and band gap energy of the as-obtained system. The hematite decomposition is enhanced due to the smaller hematite grain size. The crystallization of hematite and In2O3 was suppressed, with drops of enthalpy values due to the stronger solid-solid interactions after ball milling, which caused gradual In3+-Fe3+ substitution in hematite/In2O3 lattices. The band gap for hematite shifts to higher energy value, while that of indium oxide shifts to lower energy value after ball milling.

Oxalates containing various 3d transitional elements and positive NH(4) or negative OH groups were newly synthesized. Each above-mentioned component has directly influenced the structure, the electronic or interaction properties, while some unexpected behaviors were revealed by various magnetic and Mossbauer measurements. The main magnetic parameters, the long-range anti-ferromagnetic couplings observed at very low temperature and, particularly the uncompensated moment are discussed in detail. The induced lower spin states for bivalent ions and especially the anti-parallel arrangement of the spins belonging to trivalent and bivalent iron inside the molecule are also emphasized. (C) 2010 Elsevier B.V. All rights reserved.

The ultraviolet, visible, and near IR (0.8-2.4 mu m) luminescence spectra of BaY2F8 single crystals heavily doped with Ho3+ ions (10 and 30 mol%) have been investigated at room temperature and 12 K, together with the luminescence decay curves (up to 300 mu s) of the visible emission. Excitation in the visible region gives rise to very strong emission bands originating from the first I-5(7) level and located around 2070 nm. However the I-5(7) emission is not observed upon excitation at wavelengths shorter than 300 nm. The inter-ionic processes are found to shorten the decay times of the levels emitting in the visible region with respect to the corresponding radiative lifetimes. (C) 2010 Elsevier B.V. All rights reserved.

The quantum efficiency of the absorption on quantum confinement levels is investigated. This is achieved by modeling the electron confinement in a spherical quantum dot (QD). The confinement levels are calculated using both infinite and finite rectangular quantum wells. The spectral internal quantum efficiency is evaluated within both the models, by computing Einstein's coefficients for the transitions between confinement levels. The size of QDs (1-3 nm radius) leads to negligible many body effects. The nature of the QD material and of the matrix embedding is taken into account in the finite rectangular quantum well approximation and introduces only a small correction. The temperature dependence of the efficiency is also taken into account. A numerical application is performed for a silicon QD of 2.5 nm radius, embedded in amorphous silica. It is proved that the absorption threshold shifts toward the far infrared limit and that the spectral internal quantum efficiency reaches 4-5% at the threshold.

We investigated the relaxation of the irreversible magnetization in a series of 200 nm thick YBa2Cu3O7/PrBa2Cu3O7 [(YBCO)(n)/(PrBCO)(m)] superlattices, where the thickness m of the nonsuperconducting PrBCO layer (measured in unit cells) was kept to m = 4 (sufficient to decouple the superconducting YBCO layers), whereas the thickness n of the YBCO layer was varied between 2 and 20 unit cells. The analysis of standard zero-field-cooling dc magnetization relaxation data obtained in the low temperature T region with the applied magnetic field H oriented along the c axis reveals the occurrence of a crossover elastic (collective) vortex creep at low T-plastic vortex creep at high T, generated by the T dependent macroscopic currents induced in the sample during measurements. For thin superlattices (n < 20) the creep crossover temperature T-cr proportional to n, and T-cr decreases linearly with increasing ln(H) for a fixed n. This crossover represents an alternative to the elastic vortex glass behavior reported for superlattices, as well as to 'quantum vortex creep' at unexpectedly high T inferred for thin films. We also discuss the absence of an increase of the magnetically determined critical current density with decreasing YBCO thickness in our superlattices, which apparently contradicts the collective pinning theories.