P T-symmetry breaking in dual-core phosphate-glass photonic crystal fibers.

We investigate the properties of a soft glass dual-core photonic crystal fiber for application in multicore waveguiding with balanced gain and loss. Its base material is a phosphate glass in a P2O5-Al2O3-Yb2O3-BaO-ZnO-MgO-Na2O oxide system. The separated gain and loss cores are realized with two cores with ytterbium and copper doping of the base phosphate glass. The ytterbium-doped core supports a laser (gain) activity under excitation with a pump at 1000 nm wavelength, while the CuO-doped is responsible for strong attenuation at the same wavelength. We establish conditions for an exact balance between gain and loss and investigate pulse propagation by solving a system of coupled generalized nonlinear Schrödinger equations. We predict two states of light under excitation with hyperbolic secant pulses centered at 1000 nm: 1) linear oscillation of the pulse energy between gain and loss core (P T-symmetry state), with strong power attenuation; 2) retention of the pulse in the excited gain core (broken P T-symmetry), with very modest attenuation. The optimal pulse energy levels were identified to be 100 pJ (first state) and 430 pJ (second state).

Analysis of high-contrast all-optical dual-wavelength switching in asymmetric dual-core fibers.

We systematically present experimental and theoretical results for the dual-wavelength switching of 1560 nm, 75 fs signal pulses (SPs) driven by 1030 nm, and 270 fs control pulses (CPs) in a dual-core fiber (DCF). We demonstrate a switching contrast of 31.9 dB, corresponding to a propagation distance of 14 mm, achieved by launching temporally synchronized SP-CP pairs into the fast core of the DCF with moderate inter-core asymmetry. Our analysis employs a system of three coupled propagation equations to identify the compensation of the asymmetry by nonlinearity as the physical mechanism behind the efficient switching performance.

Alkylation of Nitroarenes via Vicarious Nucleophilic Substitution - Experimental and DFT Mechanistic Studies.

Alkylation of nitroarenes via Vicarious Nucleophilic Substitution (VNS) was tested experimentally and modelled with DFT calculations. Mechanistic studies reveal intrinsic differences between reactions of archetypal carbanion precursor PhSO2 CH2 Cl, and alkyl phenyl sulfones, in which benzenesulfinate acts as a leaving group. Accordingly, for the latter precursors steric hindrance develops at the ß-elimination step, that raises energy barrier and results in the formation of byproducts.

Electrochemical Determination of Nanoparticle Size: Combined Theoretical and Experimental Study for Matrixless Silver Nanoparticles.

A chronoamperometric procedure for the preparation of silver nanoparticles (AgNPs) in aqueous systems with no extra added stabilizing agents is presented. The uniqueness of the prepared nanoparticle systems was explored by theoretical considerations. The proposed theoretical model predicts the structural parameters of the obtained nanoparticle system. The parameters required for the calculations (the zeta potential, conductivity, and effective diffusion coefficient of ionic silver) are available from independently performed measurements. Chronoamperometry at a microelectrode was employed for the evaluation of the effective diffusion coefficient of ionic silver present in the AgNP solution. The values of AgNP radii predicted by the theoretical model for the selected samples were compared to those obtained by Transmission Electron Microscopy (TEM) and Dynamic Light Scattering (DLS) methods. Because of the high polydispersity of the prepared nanoparticle samples, DLS results were overestimated in comparison to both: the TEM results and some theoretical predictions. By correcting the theoretical predictions by the Debye length, the calculated nanoparticle sizes become comparable (within their expanded uncertainties) to those measured in TEM images, especially for the nanosystems at early stages of their formation via the electrosynthesis process.