Aeppli and Bott–Chern cohomology for bi-generalized Hermitian manifolds and d′d″-lemma

We define Aeppli and Bott–Chern cohomology for bi-generalized complex manifolds and show that they are finite dimensional for compact bi-generalized Hermitian manifolds. For totally bounded double complexes $(A,d^{\prime }{d}^{″})$, we show that the validity of $d^{\prime }{d}^{″}$-lemma is equivalent to having the same dimension of several cohomology groups. Some calculations of Bott–Chern cohomology groups of some bi-generalized Hermitian manifolds are given.     

Internal pair creation induced by nuclear coulomb excitation in heavy-ion collisions

Internal electron-positron pair creation caused by nuclear Coulomb excitation in heavy-ion collisions is compared with the spontaneous and induced positron production in overcritical quasimolecules with Z₁ + Z₂$?170. Using the rotation-vibration nuclear model in the calculation of the quadrupole Coulomb excitation and the conversion coefficient for electron-positron pair formation, the total cross section for the system ²³⁸₉₂U-²³⁸₉₂U was found to be ${\sigma }_C^{e^{+},e^{?}}=0.125mb$ at E_kin^c.m. = 797 MeV, which is four times smaller than the cross section ${\sigma }_{ind}^{e^{+},e^{?}}$ for the corresponding vacuum decay process if a K-shell vacancy production of L₀ = 10^? is assumed. Evaluation of the ratio $R=d{\sigma }_{ind}^{e^{+},e^{?}}({?}_{c.m.})/d{\sigma }_C^{e^{+},e^{?}}({?}_{c.m.})$ between the differential cross sections with respect to the ion angle ?_c.m leads to R = 60 at ?_c.m. = 160°. In contrast to the induced positron spectrum, the decay of excited nuclear levels in U is not followed by positrons with kinetic energy above 0.9 MeV. Therefore a unique determination of the decay of the vacuum in overcritical fields is experimentally possible provided that L₀ is not drastically reduced. In addition, similar calculations have been performed for pair creation resulting from nuclear Coulomb excitation for the systems U-Cf, Th-Th, Pb-Pb, Ni-Ni, Xe-Ba, Xe-Nd and Xe-Ce. The occupation of vacant bound states of superheavy electronic molecules by conversion electrons of γ-rays from nuclear transitions with E_γ < 1 MeV is also discussed.     

Pressure dependence of negative thermal expansion in Zr2(WO4)(PO4)2

Negative thermal expansion materials can experience significant stresses when they are used in composites. Under ambient conditions Zr₂(WO₄)(PO₄)₂ displays anisotropic negative thermal expansion (NTE) (${\alpha }_v=?14.0\left(10\right)\times 10^{?6}{K}^{?1}$, ${\alpha }_a=?7.9\left(5\right)\times 10^{?6}{K}^{?1}$, ${\alpha }_b=2.5\left(5\right)\times 10^{?6}{K}^{?1}$, ${\alpha }_c=?8.7\left(2\right)\times 10^{?6}{K}^{?1}$ at 0 GPa). The effect of hydrostatic pressure on its thermal expansion characteristics was investigated by neutron diffraction between 300 and 60 K at pressures up to 0.3 GPa. No phase transitions were observed in the pressure and temperature range examined. The material was found to have a bulk modulus, B₀, of 61.3(8) GPa at ambient temperature, and unlike some other NTE materials, pressure had no detectable effect on thermal expansion (${\alpha }_v=?14.2\left(8\right)\times 10^{?6}{K}^{?1}$, ${\alpha }_a=?7.9\left(3\right)\times 10^{?6}{K}^{?1}$, ${\alpha }_b=2.9\left(5\right)\times 10^{?6}{K}^{?1}$, ${\alpha }_c=?9.2\left(2\right)\times 10^{?6}{K}^{?1}$ at 0.3 GPa).     

Compressibility of hexagonal selenium to 45 kbar

Compression data to 45 kbar have been obtained for hexagonal selenium by static methods in a piston-cylinder apparatus. Cylindrical samples (1 cm dia. and 1·2 cm length) of polycrystalline hexagonal selenium, with a bulk density close to the X-ray density, were prepared by pressing the samples at 7 kbar and 170°C. The compression data are described by a third degree polynomial,

$?\left(\frac{\Delta V}{V_O}\right)=?64·14\times {10}^{?4}P+109·9\times {10}^{?6}{P}^2?96·77\times {10}^{?8}{P}^3$

,where P is pressure in kbar. The zero pressure bulk modulus and the pressure derivative of the bulk modulus are 156 ± 10 kbar and 4·33 respectively.     

Lattice dynamics and phase transition of NiTi alloy

We have performed detailed first-principles calculations to investigate the structural and lattice dynamical properties of NiTi alloy. The calculated static structures consist well with the experimental data and other theoretical results. With quasi harmonic approximation, the phase boundary between B19′ and BCO phases can be described as a five order polynomial $T=100?89.28P+296.75P^2?717.94P^3+734.62P^4?274.25P^5$. The change of vibrational entropy is $0.07k_B$/atom at the transition temperature 100 K under zero pressure.     

Detecting switching points using asymmetric detrended fluctuation analysis

This work uses the concept of Asymmetric Detrended Fluctuation Analysis (A-DFA) to investigate and characterize the occurrence of trend switching in financial series. A-DFA introduces two new roughness exponents, $H^{+}$ and $H^{?}$, which differ from the usual one $H$ by separately taking into account contributions to the fluctuations according to whether the local trend is, respectively, upward or downward. The developed methodology requires the evaluation of local values of $H\left(t\right),H^{+}\left(t\right)$, and $H^{?}\left(t\right)$, by restricting the size of the largest window around the value $t$. We show that $H^{+}\left(t\right)$ and $H^{?}\left(t\right)$ behave differently in the neighborhoods of switching points (SPs) where trends change sign. Properly taken differences between shifted local values of $H\left(t\right),H^{+}\left(t\right)$, and $H^{?}\left(t\right)$ allow to identify and characterize SP’s. Tests with Weiertrasse functions, isolated peaks, and actual financial series are presented, supporting the validity of the proposed method.     

Thermoelectric and topological properties of half-Heusler compounds ZrIrX(As,Sb, Bi)

The strain dependent electronic structures, thermoelectric and topological properties of the half-Heusler compounds ZrIrX(X=As, Sb, Bi) are investigated by the first-principle calculations. At the equilibrium lattice constants, all the three compounds are trivial insulators and good thermoelectric materials with the Seebeck coefficient S and the power factor over relaxation time $S^2\sigma /\tau$ as large as 1180 (μV/K) and 4.1 (${10}^{11}W{m}^{?1}{K}^{?2}{s}^{?1}$), respectively. The compressive strain enhances the band gap, while the tensile strain decreases the band gap. At some specific tensile strains, the compounds become Dirac-semimetals, with the s-type band ${\mathrm{\Gamma }}_6$ below p-type band ${\mathrm{\Gamma }}_8$, in the cubic phase. When we compress the a(b)-axis and elongate the c-axis of the compounds, they become the type-I Weyl semimetals. For ZrIrAs, the eight Weyl-Points (WPS) locate at (± K_x, 0, ± K_z), (0, ± K_y, ± K_z), ${\mathrm{K}}_x={\mathrm{K}}_y=0.008{\mathrm{\AA }}^{?1}$, ${\mathrm{K}}_z=0.043{\mathrm{\AA }}^{?1}$.     

Microcanonical solution of the mean-field φ4 model: Comparison with time averages at finite size

We study the mean-field ${\phi }^4$ model in an external magnetic field in the microcanonical ensemble using two different methods. The first one is based on Rugh's microcanonical formalism and leads to express macroscopic observables, such as temperature, specific heat, magnetization and susceptibility, as time averages of convenient functions of the phase-space. The approach is applicable for any finite number of particles N. The second method uses large deviation techniques and allows us to derive explicit expressions for microcanonical entropy and for macroscopic observables in the $N\to \infty$ limit. Assuming ergodicity, we evaluate time averages in molecular dynamics simulations and, using Rugh's approach, we determine the value of macroscopic observables at finite N. These averages are affected by a slow time evolution, often observed in systems with long-range interactions. We then show how the finite N time averages of macroscopic observables converge to their corresponding $N\to \infty$ values as N is increased. As expected, finite size effects scale as $N^{-1}$.     

One-photon absorption in direct gap semiconductors

One-photon absorption coefficients of InSb and GaAs are calculated using the first order perturbation theory assuming a two band model in which the interband energy difference is given by $E(k)=E_g{(1+\frac{h^2{k}^2}{m^{*E}g})}^{1/2}$ The results obtained are in much better agreement with the experimental data than the results of first order perturbation calculations using parabolic bands.