Broad spectral sliced multiwavelength source with a mode locked fiber laser

A simple multi-wavelength source is demonstrated based on spectral slicing of supercontinuum (SC) light using a Sagnac loop mirror. A mode locked fiber laser with pulse width of 800 fs is employed to generate the SC in photonic crystal fiber (PCF). The SC light extending from 1200 nm up to the wavelength region above 1750 nm is obtained at the amplified pulse pump power of 30 dBm. By slicing the SC with a loop mirror, a multiwavelength comb spectrum is obtained with different channel spacing for different operating wavelength region. Spacings of 1.5, 2.3, and 2.9 nm are shown at wavelength regions of 1220, 1450, and 1730 nm, respectively. It is also observed that the signal to noise ratio (SNR) increases from 15 to 20 dB as the operating wavelength increases from 1220 to 1730 nm region.     

Time delay reduction in low power ultrashort pulse and pulse stream propagation with overlapping soliton pair

Propagation of temporal 50 femtosecond pulse and pulse stream, which is realized by substituting each input pulse with reduced-order overlapping soliton pair, is investigated through short standard single-mode fiber. For the pulse stream the initial inter-pulse delay is selected to be 227 fs and the pulses are to be perturbed to avoid collision with the neighboring pulses. This method reduces the pulse time delay and properly retains the amplitude despite tradeoff between these two. This is a significant improvement in the low power femtosecond pulse and pulse stream propagation.     

Magnetic and structural studies on CoFe2O4 nanoparticles synthesized by co-precipitation,normal micelles and reverse micelles methods

Cobalt ferrite nanoparticles were synthesized by the chemical co-precipitation, normal micelles and reverse micelles methods of iron and cobalt chlorides. X-ray diffraction analysis, Fourier Transform Infrared (FTIR) and Vibrating Sample Magnetometer were carried out at room temperature to study the structural and magnetic properties. X-ray patterns revealed the production of a broad single cubic phase with the average particle sizes of ∼12 nm, 5 nm and 8 nm for co-precipitation, normal micelles and reverse micelles methods, respectively. The FTIR measurements between 400 and 4000 cm⁻¹ confirmed the intrinsic cation vibrations of spinel structure for each one of the three methods. Moreover, the average particle sizes were lower than the single domain size (128 nm) and higher than the super-paramagnetic size (2–3 nm) at room temperature. The results revealed that the magnetic properties depend on the particle size and cation distribution, whereas the role of particle size is more significant.     

The effect of doping three Al and N atoms on the chemical shielding tensor parameters of the boron phosphide nanotubes: A DFT study

In this work, an armchair model of the (4,4) boron phosphide nanotubes (BPNTs) with a 1-nm length and consisting of 32 B and 32 P atoms is considered to study the influence of doping three atoms of aluminum in sites of boron (B_3AlPNTs) and three atoms of nitrogen in sites of phosphors (BP_3NNTs) on the electrostatic structure properties. The mouths of nanotubes are capped by hydrogen atoms in order to saturate the dangling bonds of the boundaries and to decrease the calculation time. The structures of BPNTs, B_3AlPNTs and BP_3NNTs are optimized by performing the level of density functional theory (DFT) using 6-31G^? basis set. The optimized structures are used for calculating the chemical shielding (CS) tensors and nuclear magnetic resonance parameters such as isotropic chemical shielding (CS^I) and anisotropic chemical shielding (CS^A). The results reveal that in both models of B_3AlPNTs and BP_3NNTs by doping N atoms the chemical shielding parameters of P and B atoms, which are directly connected to the Al and N atoms decreased and the other sites significantly changed.     

Modeling semiconductor devices by using Neuro Space Mapping

In this paper a new method for modeling semiconductor devices by use of the drift-diffusion (DD) model and neural networks is presented. Unlike the hydrodynamic (HD) model which is complicated, time consuming with high processing cost, the proposed method has lower complexity and lower simulation time. In this method the RBF neural network has been used for correcting parameters in the drift-diffusion model. Therefore solving approximate model (DD) causes to obtain accurate response. The proposed method is first applied to a silicon n-i-n diode in one dimension, and then to a silicon thin-film MOSFET in two-dimensions, both for interpolation and extrapolation. The obtained results for basic variables, i.e., electron and potential distribution for different voltages, confirm the high efficiency of the proposed method.     

A novel signal extraction approach for filtering and forecasting noisy exponential series

The coefficients of Linear Recurrent Relations (LRR) play a pivotal role in many forecasting techniques. Precise and closed form of the LRR coefficients enables one to achieve more accurate forecasts. On account to the fact that, in real-world situations, a time series data is contaminated with noise, extracting the noiseless series is of great importance. This paper seeks to obtain a closed form, with less noise level, of LRR coefficients for noisy exponential time series. Improving the filtering performance through employing noiseless eigenvectors of the covariance matrix is another novelty of this study. Our simulation results confirm that the proposed approach enhances filtering and forecasting results.     

Kinetics of MTO-catalyzed olefin epoxidation in ambient temperature ionic liquids: UV/Vis and 2H NMR study

The kinetics of oxygen-atom transfer from the peroxo complexes of methyltrioxorhenium (MTO) to alkenes in ionic liquids have been investigated. Noncatalytic conversions of alkenes to epoxide were monitored by UV/Vis at 360 nm, where the monoperoxorhenium (mpRe) and diperoxorhenium (dpRe) complexes absorb. Water- and peroxide-free dpRe was prepared in situ by the reaction of MTO and urea hydrogen peroxide (UHP) in dry THF. The observed biexponential time profiles in conjunction with kinetic modeling allow the assignment of the fast step to the reaction of olefin with dpRe (k4) and the slow step to the analogous reaction with mpRe (k3). In most of the tudied ionic liquids, k4 approximately 5 x k3. 2H NMR experiments conducted with [D3]dpRe under non-steady-state conditions confirm the speciation of the catalytic system in ionic liquids and assert the validity of the UV/Vis kinetics. Deuteriated alkenes were used to study the catalytic epoxidation and dihydroxylation of alkenes by 2H NMR spectroscopy. The values of k4 for alpha-methylstyrene in several ionic liquids exceed what is observed in acetonitrile by an order of magnitude. While the rate of olefin epoxidation is unaffected by the nature of the ionic liquid cation, a discernible kinetic effect is observed with coordinating anions such as nitrate.     

Kinetics and mechanistic studies of anticarcinogenic bisperoxovanadium(V) compounds: ligand substitution reactions at physiological pH and relevance to DNA interactions

Bisperoxovanadium(V) compounds with bidentate ligands have shown tumor growth inhibition by cleaving DNA. The kinetics and mechanisms of ligand substitution reactions of two bisperoxovanadium(V) compounds [VO(O(2))(2)(bpy)](-) (bpVbpy) and [VO(O(2))(2)(phen)](-) (bpVphen) with entering ligands picolinic acid (pic) and dipicolinic acid (dipic) at physiological pH are reported, and its relevance to their DNA-cleavage activities are discussed. The products of the ligand substitution reactions with pic and dipic are the monoperoxo complexes [VO(O(2))(pic)(2)](-) and [VO(O(2))(dipic)(H(2)O)](-), respectively. (51)V NMR experiments indicate that bpVphen is substantially more inert in aqueous solution than bpVbpy. As a result, bpVbpy is more prone to ligand substitution and subsequent conversion to monoperoxo species. The rate of reaction for bpVbpy was faster than that of bpVphen by an order of magnitude, indicating that the ancillary ligand plays an important role in ligand substitution reactions. The ligand substitution reactions of bpVbpy feature first-order dependence on both [pic](T) and [dipic](T) whereas the substitution kinetics of bpVphen feature saturation behavior with dipic. The substitution reactions of both bpVbpy and bpVphen with pic showed first-order dependence on [H(+)] whereas no acid dependence was observed for the reactions with dipic. Hydrogen peroxide was determined to be a competitive inhibitor with respect to dipic. The ligand substitution reaction mechanisms and the rate laws consistent with these results are presented. The substitution reactions with pic and dipic proceed through different mechanisms; the substitution reactions with dipic proceed via solvolysis as the first step in the mechanisms whereas the reactions with pic bypass solvolysis to go through a mixed ligand monoperoxo vanadium intermediate.