Extension of the Jones matrix formalism to higher-order transverse modes

The well-known Jones matrix formalism, which can be directly applied to the propagation of the polarization of fundamental (TEM(00)) laser resonator modes, has to be modified for higher-order transverse modes. It is shown that this can be done in straightforward manner by using N x N matrices instead of the 2 x 2 Jones matrices, where N denotes the number of orthogonal polarization states of the transverse mode under consideration. The most common case of TEM(01) Hermite-Gaussian modes, where N is four, is discussed in detail.     

Numerical analysis of electronic conductivity in graphene with resonant adsorbates: comparison of monolayer and Bernal bilayer

We describe the electronic conductivity, as a function of the Fermi energy, in the Bernal bilayer graphene (BLG) in presence of a random distribution of vacancies that simulate resonant adsorbates. We compare it to monolayer (MLG) with the same defect concentrations. These transport properties are related to the values of fundamental length scales such as the elastic mean free path L _e , the localization length ξ and the inelastic mean free path L _i . Usually the later, which reflect the effect of inelastic scattering by phonons, strongly depends on temperature T. In BLG an additional characteristic distance l ₁ exists which is the typical traveling distance between two interlayer hopping events. We find that when the concentration of defects is smaller than 1%–2%, one has l ₁ ≤ L _e ? ξ and the BLG has transport properties that differ from those of the MLG independently of L _i (T). Whereas for larger concentration of defects L _e <l ₁ ? ξ, and depending on L _i (T), the transport in the BLG can be equivalent (or not) to that of two decoupled MLG. We compare two tight-binding model Hamiltonians with and without hopping beyond the nearest neighbors.     

Antimicrobial and antitumor activities of 1,2,4‐triazoles/polypyrrole chitosan core shell nanoparticles

Combination of natural biodegradable polymer with a synthetic polymer offers excellent properties for the support in drug delivery system. For this purpose, biodegradable conductive nanoparticle polypyrrole based on chitosan (PPC) has been prepared via oxidative polymerization of pyrrole in presence of chitosan using FeCl₃ as oxidant in acidic medium and used as a carrier for 1,2,4‐triazoles. The resultant nanoparticles were characterized by X‐ray diffraction, Fourier transform infrared analysis, transmission electron microscopy, scanning electron microscopy, and thermal gravimetric analysis. The results indicate that spherical nanoparticle of average diameter 52 ± 8 nm was successfully prepared. The spherical particles were composed of dark sphere surrounded by grey shell. A circumferential dark ring is observed in the shell after loading 1,2,4‐triazoles into PPC nanoparticles. The loaded triazoles were released almost linearly against time in a sustained fashion into different pH media. The mechanism of triazoles release was determined using different kinetics equations. The antibacterial activities against the gram‐negative and gram‐positive bacteria were examined. Furthermore, the antitumor activity of PPC nanoparticles loaded 1,2,4‐triazoles was also examined against Ehrlich ascites carcinoma cells and breast cancer cell line (MCF7). Polypyrrole chitosan loaded nanoparticles exhibited higher antitumor activity than 1,2,4‐triazoles.     

The master equation for a two-level atom in a laser field with squeezing-like terms

In this paper, we derive the time dependent solution of the effective master equation for the reduced density matrix operator of a two-level atom driven by a strong classical field and damped into a “modelled” reservoir with non-flat density of modes. The effects of different parameters on the atomic inversion, the von Neumann entropy and the entropy squeezing are discussed.     

Structural,luminescence and biological studies of trivalent lanthanide complexes with N,N′-bis(2-hydroxynaphthylmethylidene)-1,3-propanediamine Schiff base ligand

New eight lanthanide metal complexes were prepared. These complexes were characterized by elemental analysis, molar conductivity measurements, spectral analysis (¹H NMR, FT-IR, UV–vis), luminescence and thermal gravimetric analysis. All Ln(III) complexes were 1:1 electrolytes as established by their molar conductivities. The microanalysis and spectroscopic analysis revealed eight-coordinated environments around lanthanide ions with two nitrate ligands behaving in a bidentate manner. The other four positions were found to be occupied with tetradentate L_III ligand. Tb–L_III and Sm–L_III complexes exhibited characteristic luminescence emissions of the central metal ions and this was attributed to efficient energy transfer from the ligand to the metal center. The L_III and Ln–L_III complexes showed antibacterial activity against a number of pathogenic bacteria.     

D3→FJ emission of Tb doped sol–gel silica

Amorphous silica samples doped with 0.1 and 1 mol% of terbium (Tb) were synthesized by the sol–gel method. In addition to the green light associated with ⁵D₄→⁷F_J transitions of Tb³⁺, the sample containing 0.1 mol% also emitted blue light as a result of ⁵D₃→⁷F_J transitions during photoluminescence (PL) measurements. As a result of concentration quenching this blue emission was not observed for the samples doped with the higher concentration (1 mol%). However the blue ⁵D₃ →⁷F_J emission was observed in the 1 mol% doped samples during cathodoluminescence (CL) measurements. Since a rough calculation indicated that the excitation rate in the CL system where the blue emission is observed may be similar to a laser PL system under conditions where the blue emission is not observed, the difference is attributed to the nature of the excitation sources. It is suggested that during the CL excitation incident electrons can reduce non-luminescent Tb⁴⁺ ions in the silica, substituting for Si⁴⁺ ions, to the excited (Tb³⁺)? state and that these are responsible for the blue emission, which does not occur during PL excitation.     

Dual-channel spectral subtraction algorithms based speech enhancement dedicated to a bilateral cochlear implant

In this paper, two speech enhancement algorithms (SEAs) based on spectral subtraction (SS) principle have been evaluated for bilateral cochlear implant (BCI) users. Specifically, dual-channel noise power spectral estimation algorithm using power spectral densities (PSD) and cross power spectral density (CPSD) of the observed signals was studied. The enhanced speech signals were obtained using either Dual Channel Non Linear Spectral Subtraction ‘DC-NLSS’ or Dual-Channel Multi-Band Spectral Subtraction ‘DC-MBSS’ algorithms. For performance evaluation, some objective speech assessment tests relying on Perceptual Evaluation of Speech Quality (PESQ) score and speech Itakura-Saito (IS) distortion measurement were performed to fix the optimal number of frequency band needed in DC-MBSS algorithm. In order to evaluate the speech intelligibility, subjective listening tests were assessed with 50 normal hearing listeners using a specific BCI simulator and with three deafened BCI patients. Experimental results, obtained using French Lafon database corrupted by an additive babble noise at different Signal-to-Noise Ratios (SNR), showed that DC-MBSS algorithm improves speech understanding better than DC-NLSS algorithm for single and multiple interfering noise sources.     

Study of the critical current density and the thermodynamic critical field in deuterated κ-(BEDT-TTF)2Cu[N(CN)2]Br organic superconductor

ABSTRACT

We have studied the reversible and irreversible part of the hysteresis loops as a function of slow cooling rate through the order–disorder transformation near 80?K for the deuterated (κ-D₈-Br) κ-(BEDT-TTF)₂Cu[N(CN)₂]Br organic superconductor. We estimated the critical current density J_C and the thermodynamic critical field H_C from the magnetic hysteresis loops. Temperature dependence of the critical current density derived from the irreversible part using Bean’s model. The thermodynamic critical field H_C has been obtained from the reversible part of the hysteresis loops.     

Structural study of NiXMg1–XFe2O4 ferrites

The ferrite system Ni _x Mg_1-x Fe₂O₄ with 0≤x≤1 was prepared using the usual ceramic technique. The prepared samples were studied by X-ray diffraction and IR spectroscopy. X-ray diffraction analysis proved that all the samples were single-phase with the cubic spinel structure. The lattice constant, radius of the tetrahedral ion, unshared octahedral edge, tetrahedral bond and tetrahedral edge decrease while the bulk and theoretical densities, radius of octahedral ion, octahedral bond and shared octahedral edge increase as nickel ion substitution increases. The positions and intensities of the four bands of IR absorption spectra characterizing ferrites are composition dependent.     

Microstructural and optical properties of europium-doped zinc oxide nanowires

Single-crystal Eu³⁺-doped wurtzite ZnO micro- and nanowires were synthesized by chemical vapor deposition. The nanostructures grew via a self-catalytic mechanism on the walls of an alumina boat. The structure and properties of the doped ZnO were characterized using X-ray diffraction, energy-dispersive X-ray spectroscopy, scanning and transmission electron microscopy, and photoluminescence (PL) methods. A 10-min synthesis yielded vertically grown nanowires of 50–400 nm in diameter and several micrometers long. The nanowires grew along the ±[0001] direction. The Eu³⁺ concentration in the nanowires was 0.8 at.%. The crystal structure and microstructure of were compared for Eu³⁺-doped and undoped ZnO. PL spectra showed a red shift in emission for Eu³⁺-doped (2.02 eV) compared to undoped ZnO nanowires (2.37 eV) due to Eu³⁺ intraionic transitions. Diffuse reflectance spectra revealed widening of the optical bandgap by 0.12 eV for Eu³⁺-doped compared to undoped ZnO to yield a value of 3.31 eV. Fourier-transform infrared spectra confirmed the presence of europium in the ZnO nanowires.