Lie-theoretic generating relations of two variable Laguerre polynomials

Generating relations involving two variable laguerre polynomials L_n(x, y) are derived. The process involves the construction of a three-dimensional Lie algebra isomorphic to special linear algebra sl(2) with the help of Weisner's method by giving suitable interpretations to the index n of the polynomials L_n(x, y).     

The Fixed Point of a Generalization of the Renormalization Group Maps for Self-Avoiding Paths on Gaskets

Let W(x,y) = ax ³+ bx ⁴+ f ₅ x ⁵+ f ₆ x ⁶+ (3 ax ²)² y+ g ₅ x ⁵ y + h ₃ x ³ y ² + h ₄ x ⁴ y ² + n ₃ x ³ y ³+a ₂₄ x ² y ⁴+a ₀₅ y ⁵+a ₁₅ xy ⁵+a ₀₆ y ⁶, and X = , , where the coefficients are non-negative constants, with a > 0, such that X ²(x,x ²)−Y(x,x ²) is a polynomial of x with non-negative coefficients. Examples of the 2 dimensional map Φ: (x,y)↦ (X(x,y),Y(x,y)) satisfying the conditions are the renormalization group (RG) maps (modulo change of variables) for the restricted self-avoiding paths on the 3 and 4 dimensional pre-gaskets. We prove that there exists a unique fixed point (x _f ,y _f ) of Φ in the invariant set . 2000 Mathematics Subject Classification Numbers: 82B28; 60G99; 81T17; 82C41.     

Li and Nb codoping in dielectric properties and phase transitions of KTaO3: Reentrant dipolar glass and long-range dipole ordering

Abstract

The highly polarizable perovskite-type oxide, KTaO₃ doped simultaneously with Li⁺ and Nb⁵⁺ (K_1?xLi_xTa_1?yNb_yO₃, KLTN), reveals unexpected properties and ordering effects. Studies of the dielectric permittivity ?'(T, f) (10—300K, 100Hz-1 MHz) for x = 0.0014 and y = 0.024 show collective dipolar ordering effects with a transition from paraelectric into a mixed phase (coexisting dipole-glass-like and long-range ordered ferroelectric phases) taking place near 39 K. At 15 K another phase transition into a reentrant dipolar glass-like state is observed. Such a sequence of transitions and the existence of a reentrant glass state are unknown for electrical dipolar systems.     

Instability Zones of a Periodic 1D Dirac Operator and Smoothness of its Potential

Let L be the differential operatorwhere P(x),Q(x) are 1-periodic functions such that The operator L, considered on [0,1] with periodic (y(0)=y(1)), or antiperiodic (y(0)=−y(1)) boundary conditions, is self-adjoint, and moreover, for large |n| it has, close to nπ, a pair of periodic (if n is even), or antiperiodic (if n is odd) eigenvalues λ⁺_n , λ^-_n. We study the relationship between the decay rate of the instability zone sequence γ_n = λ_n⁺ - λ_n^-, n → ± ∞, and the smoothness of the potential function P(x).The first author acknowledges the hospitality of The Mathematics Department of The Ohio State University during academic year 2003/2004. His research is partially supported by Grant MM–1401/04 of the Bulgarian Ministry of Education and Science.     

Effective nonlinear optical properties of shape distributed composite media

The effective linear and nonlinear optical properties of metal/dielectric composite media, in which ellipsoidal metal inclusions are distributed in shape, are investigated. The shape distribution function P(L _x, L _y) is assumed to be 2Δ^-2θ(L _x - 1/3 + Δ/3)θ(L _y - 1/3 + Δ/3)θ(2/3 + Δ/3 - L _x - L _y), where θ( ^{. . .} ) is the Heaviside function, Δ is the shape variance and L_i are the depolarization factors of the ellipsoidal inclusions along i-symmetric axes (i = x, y). Within the spectral representation, we adopt Maxwell-Garnett type approximation to study the effect of shape variance Δ on the effective nonlinear optical properties. Numerical results show that both the effective linear optical absorption α ∼ ωIm() and the modulus of the effective third-order optical nonlinearity enhancement |χ⁽³⁾ _e|/χ⁽³⁾ ₁ exhibit the nonmonotonic behavior with Δ. Moreover, with increasing Δ, the optical absorption and the nonlinearity enhancement bands become broad, accompanied with the decrease of their peaks. The adjustment of Δ from 0 to 1 allows us to examine the crossover behavior from no separation to large separation between optical absorption and nonlinearity enhancement peaks. As Δ → 0, i.e., the ellipsoidal shape deviates slightly from the spherical one, the dependence of |χ⁽³⁾ _e|/χ⁽³⁾ ₁ on Δ becomes strong first and then weak with increasing the imaginary part of inclusions' dielectric constant. In the dilute limit, the exact formula for the effective optical nonlinearity is derived, and the present approximation characterizes the exact results better than old mean field one does. Received 10 December 2002 Published online 4 June 2003 RID="a" ID="a"e-mail: lgaophys@pub.sz.jsinfo.net     

Integrability Conditions for Complex Homogeneous Kukles Systems

In this paper we study the existence of local analytic first integrals for complex polynomial differential systems of the form ? = x + P_n(x, y), ? = ?y, where P_n(x, y) is a homogeneous polynomial of degree n, called the complex homogeneous Kukles systems of degree n. We characterize all the homogeneous Kukles systems of degree n that belong to the Sibirsky ideal. Finally, we provide necessary and sufficient conditions when n = 2,?. . .?, 7 in order that the complex homogeneous Kukles system has a local analytic first integral computing the saddle constants and using Gröbner bases to find the decomposition of the algebraic variety into its irreducible components.     

Low Temperature Properties for Correlation Functions in Classical N-Vector Spin Models

We obtain convergent multi-scale expansions for the one-and two-point correlation functions of the low temperature lattice classical N - vector spin model in d S 3 dimensions, N S 2. The Gibbs factor is taken as exp[-b(1/2 ||?f||² +l/8 || |f|² - 1 ||² + v/2||f- h||²)], \exp [-\beta (1/2 ||\partial \phi||^2 +\lambda/8 ||\, |\phi|^2 - 1 ||^2 + v/2||\phi - h||^2)], where f(x), h ? R^N\phi(x), h \in R^N, x ? Z^dx \in Z^d, |h|=1, b < ￥|h|=1, \beta < \infty, l 3 ￥\lambda \geq \infty are large and 0 < v h 1. In the thermodynamic and v ˉ 0v \downarrow 0 limits, with h = e₁, and j L ‘^½ ‘, the expansion gives áf₁(x)? = 1+0(1/b^1/2)\langle \phi_1(x)\rangle = 1+0(1/\beta^{1/2}) (spontaneous magnetization), áf₁(x)f_i(y)? = 0\langle \phi_1(x)\phi_i(y)\rangle=0, áf_i (x)f_i (y)? = c₀ D^-1(x,y)+R(x,y)\langle \phi_i (x)\phi_i (y)\rangle = c_0 \Delta^{-1}(x,y)+R(x,y) (Goldstone Bosons), i = 2, 3, ?, Ni= 2, 3,\,\ldots, N, and áf₁(x)f₁(y)?^T=R￠(x,y)\langle \phi_1(x)\phi_1(y)\rangle^T=R'(x,y), where |R(x,y)||R(x,y)|, |R￠(x,y)| < 0(1)(1+|x-y|)^d-2+r|R'(x,y)|< 0(1)(1+|x-y|)^{d-2+\rho} for some „ > 0, and c₀ is aprecisely determined constant.     

Ground State Entropy of the Potts Antiferromagnet on Triangular Lattice Strips

We present exact calculations of the zero-temperature partition function (chromatic polynomial) P for the q-state Potts antiferromagnet on triangular lattice strips of arbitrarily great length L_x vertices and of width L_y vertices and, in the L_x→∞ limit, the exponent of the ground state entropy, W=e^S₀/k_B. The strips considered, with their boundary conditions (BC), are (a) (FBC_y, PBC_x) = cyclic for L_y=3, 4, (b) (FBC_y, TPBC_x) = Möbius, L_y=3, (c) (PBC_y, PBC_x) = toroidal, L_y=3, (d) (PBC_y, TPBC_x) = Klein bottle, L_y=3, (e) (PBC_y, FBC_x) = cylindrical, L_y=5, 6, and (f) (FBC_y, FBC_x) = free, L_y=5, where F, P, and TP denote free, periodic, and twisted periodic. Several interesting features are found, including the presence of terms in P proportional to cos(2πL_x/3) for case (c). The continuous locus of points where W is nonanalytic in the q plane is discussed for each case and a comparative discussion is given of the respective loci for families with different boundary conditions. Numerical values of W are given for infinite-length strips of various widths and are shown to approach values for the 2D lattice rapidly. A remark is also made concerning a zero-free region for chromatic zeros. Some results are given for strips of other lattices.     

Nonmonotonic external field dependence of the magnetization in a finite Ising model: Theory and MC simulation

Using field theory and Monte Carlo (MC) simulation we investigate the finite-size effects of the magnetization M for the three-dimensional Ising model in a finite cubic geometry with periodic boundary conditions. The field theory with infinite cutoff gives a scaling form of the equation of state where is the reduced temperature, h is the external field and L is the size of system. Below and at the theory predicts a nonmonotonic dependence of f(x,y) with respect to at fixed and a crossover from nonmonotonic to monotonic behaviour when y is further increased. These results are confirmed by MC simulation. The scaling function f(x,y) obtained from the field theory is in good quantitative agreement with the finite-size MC data. Good agreement is also found for the bulk value at . Received 20 July 1999 and Received in final form 11 November 1999     

Generalized holographic and Ricci dark energy models

In this paper, we consider generalized holographic and Ricci dark energy models where the energy densities are given as ρ _R =3c ² M _pl² Rf(H ²/R) and ρ _h =3c ² M _pl² H ² g(R/H ²), respectively; here f(x), g(y) are positive defined functions of the dimensionless variables H ²/R or R/H ². It is interesting that holographic and Ricci dark energy densities are recovered or recovered interchangeably when the function f(x)=g(y)≡1 or f(x)=Id and g(y)=Id are taken, respectively (for example f(x),g(x)=1−ε(1−x), ε=0or1, respectively). Also, when f(x)≡xg(1/x) is taken, the Ricci and holographic dark energy models are equivalent to a generalized one. When the simple forms f(x)=1−ε(1−x) and g(y)=1−η(1−y) are taken as examples, by using current cosmic observational data, generalized dark energy models are considered. As expected, in these cases, the results show that they are equivalent (ε=1−η=1.312), and Ricci-like dark energy is more favored relative to the holographic one where the Hubble horizon was taken as an IR cut-off. And the suggested combination of holographic and Ricci dark energy components would be 1.312R−0.312H ², which is 2.312H²+1.312[(H)\dot]2.312H^{2}+1.312\dot{H} in terms of H ² and [(H)\dot]\dot{H} .     

Minimum Polynomial for Single-Mode Parabose Parasupercharge and Hamiltonian

We calculate the minimum polynomial φ(x,y) of parasupercharge Q and Hamiltonian H for single-mode parabose parasupersymmetry (P-PSUSY). Suppose that φ(x,y) satisfies the homogeneity ∀ λ∈ℝ,φ(λ x,λ ² y)=λ ⁿ φ(x,y), then the parafermionic order p _f is restricted to either 1, 2, or 4. Under the P-PSUSY, the homogeneity of the φ(x,y) is equivalent to the parasuperconformality of Q and H. The physical meaning of the parasuperconformality is discussed, in connection with the spin of the elementary particle.     

Structure of the Partition Function and Transfer Matrices for the Potts Model in a Magnetic Field on?Lattice Strips

We determine the general structure of the partition function of the q-state Potts model in an external magnetic field, Z(G,q,v,w) for arbitrary q, temperature variable v, and magnetic field variable w, on cyclic, M?bius, and free strip graphs G of the square (sq), triangular (tri), and honeycomb (hc) lattices with width L _y and arbitrarily great length L _x . For the cyclic case we prove that the partition function has the form Z(L,L_y×L_x,q,v,w)=?_d=0^L_y[(c)\tilde]^(d)Tr[(T_Z,L,Ly,d)^m]Z(\Lambda,L_{y}\times L_{x},q,v,w)=\sum_{d=0}^{L_{y}}\tilde{c}^{(d)}\mathrm{Tr}[(T_{Z,\Lambda,L_{y},d})^{m}] , where Λ denotes the lattice type, [(c)\tilde]^(d)\tilde{c}^{(d)} are specified polynomials of degree d in q, T_Z,L,Ly,dT_{Z,\Lambda,L_{y},d} is the corresponding transfer matrix, and m=L _x (L _x /2) for Λ=sq,tri (hc), respectively. An analogous formula is given for M?bius strips, while only T_Z,L,Ly,d=0T_{Z,\Lambda,L_{y},d=0} appears for free strips. We exhibit a method for calculating T_Z,L,Ly,dT_{Z,\Lambda,L_{y},d} for arbitrary L _y and give illustrative examples. Explicit results for arbitrary L _y are presented for T_Z,L,Ly,dT_{Z,\Lambda,L_{y},d} with d=L _y and d=L _y −1. We find very simple formulas for the determinant det(T_Z,L,Ly,d)\mathrm{det}(T_{Z,\Lambda,L_{y},d}) . We also give results for self-dual cyclic strips of the square lattice.     

The corrections to scaling within Mazenko’s theory in the limit of low and high dimensions

We consider corrections to scaling within an approximate theory developed by Mazenko for nonconserved order parameter in the limit of low (d → 1) and high (d → ∞) dimensions. The corrections to scaling considered here follows from the departures of the initial condition from the scaling morphology. Including corrections to scaling, the equal time correlation function has the form: C(r, t) = f ₀(r/L)+L ^−ω f ₁(r/L)+…, where L is a characteristic length scale (i.e. domain size). The correction-to-scaling exponent ω and the correction-to-scaling functions f ₁(x) are calculated for both low and high dimensions. In both dimensions the value of ω is found to be ω = 4 similar to 1D Glauber model and OJK theory (the theory developed by Ohta, Jasnow and Kawasaki).     

Dilute gas viscosity of n-alkanes represented by rigid Lennard-Jones chains

ABSTRACT

The shear viscosity in the dilute gas limit has been calculated by means of the classical trajectory method for a gas consisting of chain-like molecules. The molecules were modelled as rigid chains made up of spherical segments that interact through a combination of site–site Lennard-Jones 12-6 potentials. Results are reported for chains consisting of 2, 3, 4, 6, 8, 12 and 16 segments in the reduced temperature range of 0.3–50 for site–site separations of 0.25σ, 0.333σ, 0.40σ, 0.60σ and 0.80σ, where σ is the Lennard-Jones length scaling parameter. The results were used to determine the shear viscosity of n-alkanes in the zero-density limit by representing an n-alkane molecule as a rigid linear chain consisting of n_c ? 1?spherical segments, where n_c?is the number of carbon atoms. We show that for a given n-alkane molecule, the scaling parameters ? and σ are not unique and not transferable from one molecule to another. The commonly used site–site Lennard-Jones 12-6 potential in combination with a rigid-chain molecular representation can only accurately mimic the viscosity if the scaling parameters are fitted. If the scaling parameters are estimated from the scaling parameters of other n-alkanes, the predicted viscosity values have an unacceptably high uncertainty.     

Length of the Instability Intervals for Hill's Equation

The length of instability intervals is investigated for the Hill equation y′′+ω(ω− 2∈p(x)y = 0, where p(x) has an infinite Fourier series of coefficients c _n. For any small ∈ it is shown that these lengths are completely characterized by the c _n's.     

Central Limit Theorems for Nonlinear Hierarchical Sequences of Random Variables

Let a random variable x ₀ and a function f:[a, b] ^k [a, b] be given. A hierarchical sequence {x _n :n=0, 1, 2,...} of random variables is defined inductively by the relation x _n =f(x _{n–1, 1}, x _{n–1, 2}..., x _{n–1, k} ), where {x _{n–1, i} :i=1, 2,..., k} is a family of independent random variables with the same distribution as x _n–1. We prove a central limit theorem for this hierarchical sequence of random variables when a function f satisfies a certain averaging condition. As a corollary under a natural assumption we prove a central limit theorem for a suitably normalized sequence of conductivities of a random resistor network on a hierarchical lattice.     

The 2‐matrix of the spin‐polarized electron gas: contraction sum rules and spectral resolutions

The spin‐polarized homogeneous electron gas with densities ρ_↑ and ρ_↓ for electrons with spin ‘up’ (↑) and spin ‘down’ (↓), respectively, is systematically analyzed with respect to its lowest‐order reduced densities and density matrices and their mutual relations. The three 2‐body reduced density matrices γ_↑↑, γ_↓↓, γ_a are 4‐point functions for electron pairs with spins ↑↑, ↓↓, and antiparallel, respectively. From them, three functions G_↑↑(x,y), G_↓↓(x,y), G_a(x,y), depending on only two variables, are derived. These functions contain not only the pair densities according to g_↑↑(r) = G_↑uarr;(0,r), g_↓↓(r) = G_↓↓(0,r), g_a(r) = G_a(0,r) with r = | r ₁ ‐ r ₂|, but also the 1‐body reduced density matrices γ_↑ and γ_↓ being 2‐point functions according to γ_s = ρ_sf_s and f_s(r) = G_ss(r, ∞) with s = ↑,↓ and r = | r ₁ ‐ r ^′₁|. The contraction properties of the 2‐body reduced density matrices lead to three sum rules to be obeyed by the three key functions G_ss, G_a. These contraction sum rules contain corresponding normalization sum rules as special cases. The momentum distributions n_↑(k) and n_↓(k), following from f_↑(r) and f_↓(r) by Fourier transform, are correctly normalized through f_s(0) = 1. In addition to the non‐negativity conditions n_s(k),g_ss(r),g_a(r) ≥ 0 [these quantities are probabilities], it holds n_s(k) ≤ 1 and g_ss(0) = 0 due to the Pauli principle and g_a(0) ≤ 1 due to the Coulomb repulsion. Recent parametrizations of the pair densities of the spin‐unpolarized homogeneous electron gas in terms of 2‐body wave functions (geminals) and corresponding occupancies are generalized (i) to the spin‐polarized case and (ii) to the 2‐body reduced density matrix giving thus its spectral resolutions.     

The analysis of rovibrational motion equations of a diatomic molecule in the linear regime

The motion equations of diatomic molecules are here extended from the absolute vibrational case to a more general and real rotational and vibrational (rovibrational) case. The rovibrational Hamiltonian is heuristically formed by substituting the respective number and angular momentum operators for the vibrational and rotational quantum numbers in the energy eigenvalues of a diatomic molecule which was first introduced by Dunham. The motion equations of observable quantities such as the position and linear momentum are then determined by implementing the well-known Heisenberg relation in quantum mechanics. We face with the second-order imaginary differential equations for describing the temporal variations of the relative position and the linear momentum of two oscillating atoms, which are coupled in the x–y horizontal plane. The possible rovibrational oscillations are distinguished by the three quantum numbers n, l and m associated with the energy and angular momentum quantities. It is finally demonstrated that the simultaneous solutions of rovibrational equations satisfy the energy conservation during all quantised oscillations of a diatomic molecule in space.     

The length and the relative length of tangent vectors of finsler spaces

We consider the length of a vector in a Finsler space with the fundamental function L(x,y). The length of a vector X is usually defined as the value L(x,X) of L. On the other hand, we have an essential tensor g_ij(x,y), called the fundamental tensor, and the concept of relative length |X_y| of X may be introduced by |X|_y^y = g_ij(x,y)XⁱX^j with re spect to a supporting element y. The question arises whether is L(x,X) the minimum of |X|_y or not? If there exists a supporting element y satisfying |X|_y < L(x,X), then a curve x(t) in the Finsler space will be measured shorter than the usual length, by integrating |dx/dt|_y with the field of such supporting element y(t) along the curve.     

Concerning the structural mechanism of oxygen inclusion into the lattice of titanium carbide

Variations in the unit cell occupancy of TiC_xO_y phase are considered in terms of successive oxygen inclusion into the lattice of defect carbides TiC_0.5 ? TiC_0.9. A classification of TiC_xO_y solid solutions formed and the concentration limits of their existence are presented. Three types of cubic ternary solid solutions are shown to occur in the system TiCO: solid solutions of interstitial oxygen inclusion into the initial carbide; solid solutions of oxygen inclusion—carbon and metal exclusion; and solid solutions of oxygen inclusion—oxygen substitution for carbon-carbon and metal exclusion.Specific points (inflection and breaks) on the plots where n_i is the number of atoms per unit cell, n_i = f(y) for TiC_xO_y, are accounted for by both variations in the type of solid solution and the possibility of atomic arrangement in the vicinity of these points. On the basis of the above scheme some experimental peculiarities of Ti carbide phase oxydation are explained.