Phonon-assisted tunneling and shot noise in double barrier structures in a longitudinal magnetic field

The phonon-assisted resonant tunneling is studied for the double barrier structures in a longitudinal magnetic field. Using the scattering matrix approach with an appropriate one-particle Green's function we are able to calculate the current and the zero frequency shot noise power spectrum in a large range of the magnetic field and to any order of the electron-phonon interaction. Obtained results describe well the relevant experimental data and provide new suggestions for further examinations.     

Non-oscillatory shock-capturing finite element methods for the one-dimensional compressible Euler equations

A class of shock-capturing Petrov–Galerkin finite element methods that use high-order non-oscillatory interpolations is presented for the one-dimensional compressible Euler equations. Modified eigenvalues which employ total variation diminishing (TVD), total variation bounded (TVB) and essentially non-oscillatory (ENO) mechanisms are introduced into the weighting functions. A one-pass Euler explicit transient algorithm with lumped mass matrix is used to integrate the equations. Numerical experiments with Burgers' equation, the Riemann problem and the two-blast-wave interaction problem are presented. Results indicate that accurate solutions in smooth regions and sharp and non-oscillatory solutions at discontinuities are obtainable even for strong shocks.     

Crystallization kinetics study on higher homologues of benzylidene aniline compounds: impact of phase variant on nucleation process

A systematic kinetic study leading to the crystallization process from the kinetophases (which occur prior to crystal phase) smectic B, crystal G and smectic F is performed on representative compounds of the homologous series p-phenylbenzylidene-p'-alkylanilines (PBnA) and p-n-alkoxybenzylidene-p'-alkylanilines (nO.m) these compounds are p-phenylbenzylidene-p'-nonylaniline (PB9A), p-phenylbenzylidene-p'-tetradecylaniline (PB14A), p-n-pentadecyloxybenzylidene p'-tetradecylaniline (15O.14) and p-n-octadecyloxybenzylidene-p'-nonylaniline (18O.9). The molecular mechanism and dimensionality in crystal growth from the kineto phases are computed from the Avrami equation, while the characteristic crystalline time (t*) at each crystallization temperature is deduced from the individual plots of log t vs. ΔH. The low magnitudes of the dimensionality parameter n infers the occurrence of diffusion-controlled transformations leading to the formation of plates or needles of finite size possessing impinged edges. The degree of variation in the value of n at each crystallization temperature also reveals the existence of an independent nucleation mechanism for any individual member of the series. The influence of the terminal alkyl chain lengths on the rate of crystallization is determined from a comparative study with the reported analogous compounds.     

Magnetic moments of (νi132)−n isomers in neutron-deficient lead isotopes

The magnetic moments of the 12⁺ isomers in ^{192, 196, 198, 200, 206}Pb and of the $\text{33}\text{2}{}^{\mathrm{+}}$ isomer in ²⁰⁵Pb have been measured using the PAD technique. The results for the g-factors are: g(192) = ?0.173(2), g(196) = ?0.1600(15), g(198) = ?0.1552(15), g(200) = ?0.1512(15), g(206) = ?0.1496(18), and g(205) = ?0.148(5). As all states have a rather pure $\text{(νi}{}_{\mathrm{<mtext>13</mtext><mtext>2</mtext>}}\text{)}{}^{\mathrm{?n}}$ configuration, the values reflect directly the $\text{νi}{}_{\mathrm{<mtext>13</mtext><mtext>2</mtext>}}$ orbital. They show a decrease towards the more neutron-deficient isotopes attributed to the reduced core polarisation as a result of decreasing occupation of the $\text{i}{}_{\mathrm{<mtext>13</mtext><mtext>2</mtext>}}$ neutron shell. The measured systematics are discussed regarding core polarisation, mesonic corrections, and small admixtures of core-excited states to the $\text{i}{}_{\mathrm{<mtext>13</mtext><mtext>2</mtext>}}$ wave function.     

Studies of single-neutron holes in the transitional nuclei N = 83–89: The 142Ce(d,t)141Ce and 142Ce(3He, α)141Ce pick-up reactions

The level structure of ¹⁴¹Ce up to 3.7 MeV excitation energy has been investigated by the (d, t) and (³He, α) reactions using 17 MeV deuteron and 24 MeV ³He beams respectively. The angular distributions have been analyzed with standard DWBA calculations and spectroscopic factors are deduced. The experimental information is compared to unified model calculations involving both one-particle and two-particle one-hole configurations with quadrupole and octupole vibrations of the underlying N = 82 and N = 84 core.     

Level structure of123, 125I from the 122, 124Te(3He,d) reactions

The energy levels of ¹²³I and ¹²⁵I have been studied in the ^{122, 124}Te(³He, d)^{123, 125}I reactions at 24 MeV bombarding energy. The reaction products were analysed with an Enge split-pole magnetic spectrograph. A total of 57 levels below 3.3 MeV in ¹²³I and 79 levels below 4.1 MeV in ¹²⁵I were observed. Angular distributions were measured and compared with DWBA calculations to obtain orbital angular momentum transfers and spectroscopic strengths. The results were compared to previous radioactive decay studies and to theoretical energy level calculations.     

Synthesis of 2-alkoxy 1,4-naphthoquinone derivatives as antiplatelet,antiinflammatory, and antiallergic agents

In our continuing search for novel antiplatelet, antiallergic, and antiinflammatory agents, 2-alkoxy derivatives of 1,4-naphthoquinone were prepared. Some of these compounds showed significant antiplatelet, antiallergic, and antiinflammatory activities. Among them, 2-propoxy-1,4-naphthoquinone and 2-butoxy-1,4-naphthoquinone exhibited potent inhibitory effect on neutrophil superoxide anion formation. These two compounds are worthy of further exploration.     

Numerical study of dispersing pollutant clouds in a built-up environment

In this paper, we study numerically the dispersion of a passive scalar released from an instantaneous point source in a built-up (urban) environment using a Reynolds-averaged Navier–Stokes method. A nonlinear k–? turbulence model [Speziale, C.G., 1987. On nonlinear k–l and k–? models of turbulence. J. Fluid Mech., 178, 459–475] was used for the closure of the mean momentum equations. A tensor diffusivity model [Yoshizawa, A., 1985. Statistical analysis of the anisotropy of scalar diffusion in turbulent shear flows. Phys. Fluids, 28, 3226–3231] was used for closure of the scalar transport equations. The concentration variance was also calculated from its transport equation, for which new values of Yoshizawa’s closure coefficients are used, in order to account for the instantaneous tracer release and the complex geometry. A new dissipation length-scale model, required for the modelling of the dissipation rate of concentration variance, is also proposed. The numerical results for the flow, the pollutant concentration and the concentration variance, are compared with experimental data. This data was obtained from a water-channel simulation of a full-scale field experiment of tracer dispersion through a large array of building-like obstacles known as the Mock Urban Setting Trial (MUST).     

New conjugated copolymers based on benzo[1,2‐b; 3,4‐b′]dithiophene and derivatives of benzo[g]quinoxaline for bulk heterojunction solar cells

A series of new low‐band gap copolymers based on dioctyloxybenzo[1,2‐b;3,4‐b′] dithiophene and bis(2‐thienyl)‐2,3‐diphenylbenzo[g]quinoxaline monomers have been synthesized via a Stille reaction. The effect of different functional groups attached to bis(2‐thienyl)‐2,3‐diphenylbenzo[g]quinoxaline was investigated and compared with their optical, electrochemical, hole mobility, and photovoltaic properties. Polymer solar cell (PSC) devices of the copolymers were fabricated with a configuration of ITO/ PEDOT: PSS/copolymers: PCBM (1:4 wt ratio)/Ca/Al. The best performance of the PSC device was obtained by using PbttpmobQ as the active layer. A power conversion efficiency of 1.42% with an open‐circuit voltage of 0.8 V, a short‐circuit current (JSC) of 5.73 mA cm⁻², and a fill factor of 30.9% was achieved under the illumination of AM 1.5, 100 mW cm⁻². © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011     

Conformational Preferences and the Phase Stability of Fullerene Hexa‐adducts

Molecular conformation and the assembly structure determine the spatial arrangements of the constituent units and the functions of a molecule. Although, fullerene hexa‐adducts (FHAs) have been known as functional materials with great versatility, their conformational preferences and phase stability remain a complicate issue. By choosing bithiophene (T₂) and dodecyl bithiophene (C₁₂T₂) as the peripheral units of FHA, and using microscopic, scattering and diffraction characterizations, our study reveals how the intramolecular interaction and environmental stimulus affects the conformational preferences and phase stability of FHAs.