The scaling of the decoherence factor of a qubit coupled to a spin chain driven across quantum critical points

We study the scaling of the decoherence factor of a qubit (spin-1/2) using the central spin model in which the central spin (qubit) is globally coupled to a transverse XY spin chain. The aim here is to study the non-equilibrium generation of decoherence when the spin chain is driven across (along) quantum critical points (lines) and derive the scaling of the decoherence factor in terms of the driving rate and some of the exponents associated with the quantum critical points. Our studies show that the scaling of logarithm of decoherence factor is identical to that of the defect density in the final state of the spin chain following a quench across isolated quantum critical points for both linear and non-linear variations of a parameter even if the defect density may not satisfy the standard Kibble-Zurek scaling. However, one finds an interesting deviation when the spin chain is driven along a critical line. Our analytical predictions are in complete agreement with numerical results. Our study, though limited to integrable two-level systems, points to the existence of a universality in the scaling of the decoherence factor which is not necessarily identical to the scaling of the defect density.Comment: 5 pages, 2 figures, Final and accepted versio

Anticandidal activity of some Zn(II) and Pb(II) complexes

The reactions of zinc and lead acetate with ligands HON=C(CH2)5, PhN=C(Ph)C(OH)Ph resulted in complexes of the type [M(ac)2L2] (M = Zn/Pb and L = corresponding ligand). Ligands were prepared by green methods. Complexes were characterized by proton-NMR, IR spectral studies and these spectra were compared with that of free ligands.Antifungal activity of the complexes demonstrated that the complexes [ZnII(ac)2{N(OH)=C(CH2)5}2], [PbII(ac)2{N(OH)=C(CH2)5}2] and [ZnII(ac)2{N(Ph)=C(Ph)C(OH)Ph}2] are active against Candida albicans

Reliability analysis of shallow foundations subjected to varied inclined loads

Risk and Reliability in Geotechnical Engineerin

Methyl 2-(N-Ethylamino)cyc1opentene-1- dithio-carboxylate Complexes of Pd(II), Pt(II) & Hg(II)

250-25

Ultra-narrow and widely tunable Mn^(2+) Emission from Single Nanocrystals of ZnS-CdS alloy

Extensively studied Mn-doped semiconductor nanocrystals have invariably exhibited photoluminescence (PL) over a narrow energy window of width <= 149 meV in the orange-red region and a surprisingly large spectral width (>= 180 meV), contrary to its presumed atomic-like origin. Carrying out emission measurements on individual single nanocrystals and supported by ab initio calculations, we show that Mn PL emission, in fact, can (i) vary over a much wider range (~ 370 meV) covering the deep green-deep red region and (ii) exhibit widths substantially lower (~ 60-75 meV) than reported so far, opening newer application possibilities and requiring a fundamental shift in our perception of the emission from Mn-doped semiconductor nanocrystals.Comment: 5 pages, 5 figure

Effects of ion concentration on the hydrogen bonded structure of water in the vicinity of ions in aqueous NaCl solutions

Molecular dynamics simulations of dilute and concentrated aqueous NaCl solutions are carried out to investigate the changes of the hydrogen bonded structures in the vicinity of ions for different ion concentrations. An analysis of the hydrogen bond population in the first and second solvation shells of the ions and in the bulk water is done. Although essentially no effect of ions on the hydrogen bonding is observed beyond the first solvation shell of the ions for the dilute solutions, for the concentrated solutions a noticeable change in the average number of water-water hydrogen bonds is observed in the second solvation shells of the ions and even beyond. However, the changes in the average number of hydrogen bonds are found to be relatively less when both water-water and ion-water hydrogen bonds are counted. Thus, the changes in the total number of hydrogen bonds per water are not very dramatic beyond the first solvation shell even for concentrated solutions