Nonlinear integral equations for the finite size effects of RSOS and vertex-models and related quantum field theories

Starting from critical RSOS lattice models with appropriate inhomogeneities, we derive two component nonlinear integral equations to describe the finite volume ground state energy of the massive ${\varphi }_{\mathrm{id},\mathrm{id},\mathrm{adj}}$ perturbation of the $\mathit{SU}{(2)}_k\times \mathit{SU}{(2)}_{k^{\prime }}/\mathit{SU}{(2)}_{k+k^{\prime }}$ coset models. When $k^{\prime }\to \infty$ while the value of k is fixed, the equations correspond to the current–current perturbation of the $\mathit{SU}{(2)}_k$ WZW model. Then modifying one of the kernel functions of these equations, we propose two component nonlinear integral equations for the fractional supersymmetric sine-Gordon models. The lattice versions of our equations describe the finite size effects in the corresponding lattice models, namely in the critical $\mathrm{RSOS}(k,q)$ models, in the isotropic higher-spin vertex models, and in the anisotropic higher-spin vertex models. Numerical and analytical checks are also performed to confirm the correctness of our equations. These type of equations make it easier to treat the excited state problem.     

Persistency of single-stranded DNA: The interplay between base sequences and base stacking

The chain persistency of single-stranded (ss) DNA at a high-salt limit mainly arises from the so-called base-stacking interaction between consecutive bases along the strand. Stacking is appreciable for purine–purine (e.g., A–A) and purine–pyrimidine stacks (e.g., A–T), but it is weak for pyrimidine stacks (i.e., T–T, T–C, and C–C). We study how base stacking can stiffen the strand by classifying bases into two subclasses: stacking pairs (i.e., purine–purine and purine–pyrimidine) and non-stacking (i.e., pyrimidine–pyrimidine) pairs. With this simplification, we develop an exactly solvable model for calculating the stacking-induced persistence length ${\ell }_{\mathit{stack}}$ of heterogeneous ssDNA. It is shown that ${\ell }_{\mathit{stack}}$ is mainly determined by the occurrence rate of purines; intrinsic correlations in real DNA sequences barely influence ${\ell }_{\mathit{stack}}$. Our approach leads to a reasonable estimate of ${\ell }_{\mathit{stack}}\approx 2b$–$3b$ (under typical conditions), where b is the inter-base distance.     

Numerically anticanonical divisors on Kato surfaces

The compact curves of an intermediate Kato surface $S$ form a basis of $H^2(S,\mathbb{Q})$. We present a way to compute the associated rational coefficients of the first Chern class $c_1\left(S\right)$. We get in particular a simple geometric obstruction for $c_1\left(S\right)$ to be an integral class, or equivalently index $\left(S\right)=1$. In the final part we discuss relations with some recent work of Dloussky (2011) and Oeljeklaus and Toma (2009).     

Thermoelectric power of antiferromagnetic semiconductors near the néel temperature

Thermoelectric power in antiferromagnetic semiconductors is calculated in the vicinity of the Néel temperature by assuming the presence of the well-defined propagating modes (magnon) and a temperature-dependent magnon velocity. Carriers are specified by the mobile carriers in a broad band with an isotropic effective mass. Magnons and carriers are coupled via the sd-interaction. Anomaly near T_N does not result from the diffusion term S_diff. and it is ascribed to the magnon-drag contribution S_drag which is obtained from

$S_{drag}=?{\displaystyle \sum _{\mathit{q}}\mathit{R}(\mathit{q}){\mathit{c}}_m\left(q\right)/3e}$

,where R(q) is the momentum transfer ratio between the magnon system and carriers, c_m(q) denotesthe specific heat of the magnon q. The assumed temperature dependence of the magnon velocity makesSdru divergent at T_N with T_N ? T → +0 and it might be removed in consideration of the magnon frequency spreading. Except this divergence the calculation provides a qualitative explanation for the anomalous feature in MnTe.     

An orthorhombic chromium-center in the spinel MgAl2O4

In Cr-doped MgAl₂O₄ most of the Cr³⁺-ions occupy normal B-sites. In addition to this axial center we report here the presence of an orthorhombic Cr³⁺-center. The ESR-spectra of this new center can be described by the spin Hamiltonian:

$?=\mathit{D}\left[S_z^2?\frac{1}{3}\mathit{S}\left(S+1\right)\right]+g_x\beta H_x{S}_x+g_y\beta H_y{S}_y+g_z\beta H_z{S}_z+\mathit{E}\left(S_x^2?S_y^2\right)$

, with S=3/2. The principal axes of the center are along [111]=Z, $\left[111\right]=Z,\left[1\overline{1}0\right]=Y$ and $\left[\overline{1}\overline{1}2\right]=X$. The values of the parameters are: g_z=1·950±0·005, g_x=g_y=1·915±0·015, D=+0·903cm^?1±0·003 cm^?1 and E=+0·084 cm^?1±0·005 cm^?1. The intensity of the lines is about ten times lower than that of the axial Cr³⁺-center.     

Investigations of half-metallic ferromagnetism and thermoelectric properties of cubic XCrO3 (X = Ca,Sr,Ba) compounds via first-principles approaches

In this paper, the physical aspects of the cubic phase XCrO₃ ($\mathrm{X}=\mathrm{Ca},\mathrm{Sr},\mathrm{Ba}$) perovskites are studied by employing full-potential linearized augmented plane wave plus local orbital ($\text{FP-LAPW}+\mathit{lo}$) method. These compounds have been found stable in ferromagnetic (FM) phase since they possess lower energy in FM phase compared to non-FM phase and their stability is also confirmed by calculating the enthalpy of formation (ΔH). The electronic structures of these compounds are analyzed with Trans and Blaha modified Becke–Johnson potential (TB-mBJ) for both spin up and spin down channels, which indicate their half-metallic characters. Analysis of density of states (DOS) shows major contributions of O-2p states in the valence band and Cr 3d-state in conduction band. A comparative analysis of crystal field effect ($\mathrm{\Delta }{\mathrm{E}}_{\mathrm{crystal}}$) and the exchange energies (direct ${\mathrm{\Delta }}_x(d)$ and indirect ${\mathrm{\Delta }}_x(pd)$) tells about the main part of electronic spin in ferromagnetic character. The calculated magnetic moments make these compounds favorable for spintronic applications. In the end, thermoelectric parameters are computed for 200 K–800 K temperature range to explore potential of these compounds for applications in renewable energy devices.