Dielectric relaxation of binary polar liquid mixture measured in benzene at 10 GHz frequency

The dielectric relaxation times τ _jk ’s and dipole moments μ _jk ’s of the binary (jk) polar liquid mixture of N,N-dimethyl acetamide (DMA) and acetone (Ac) dissolved in benzene (i) are estimated from the measured real σ′ _ijk and imaginary σ″ _ijk parts of complex high frequency conductivity σ* _ijk of the solution for different weight fractions w _jk ’s of 0.0, 0.3, 0.5, 0.7 and 1.0 mole fractions x _j of Ac and temperatures (25, 30, 35 and 40°C) respectively under 9.88 GHz electric field. τ _jk ’s are obtained from the ratio of slopes of σ″ _ijk -w _jk and σ′ _ijk -w _jk curves at w _jk → 0 as well as linear slope of σ″ _ijk -σ′ _ijk curves of the existing method (Murthy et al, 1989) in order to eliminate polarpolar interaction in the latter case. The calculated τ’s are in excellent agreement with the reported τ’s due to Gopalakrishna’s method. μ _jk ’s are also estimated from slopes β’s of total conductivity σ _ijk -w _jk curves at w _jk → 0 and the values agree well with the reported μ’s from G.K. method. The variation of τ _jk ’s and μ _jk ’s with x _j of Ac reveals that solute-solute molecular association occurs within 0.0–0.3x _j of Ac beyond which solute-solvent molecular association is predicted. The theoretical dipole moments μ _theo’s are calculated from bond angles and bond moments to have exact μ’s only to show the presence of inductive, mesomeric and electromeric effects in the substituent polar groups. The thermodynamic energy parameters are estimated from ln(τ _jk T) against 1/T linear curve from Eyring’s rate theory to know the molecular dynamics of the system and to establish the fact that the mixture obeys the Debye-Smyth relaxation mechanism.      

Relaxation phenomena of polar non-polar liquid mixtures under low and high frequency electric field

Simultaneous calculation of the dipole moment μ_j and the relaxation time τ_j of a certain number of non-spherical rigid aliphatic polar liquid molecules (j) in non-polar solvents (i) under 9.8 GHz electric field is possible from real ε′_ij and imaginary ε″_ij parts of the complex relative permittivity ε*_ij. The low frequency and infinite frequency permittivities ε_0ij and ε_∞ij measured by Purohitet al [1,2] and Srivastava and Srivastava [3] at 25, 35 and 30°C respectively are used to obtain static μ_s. The ratio of the individual slopes of imaginary σ″_ij and real σ′_ij parts of high frequency (hf) complex conductivity σ*_ij with weight fractionsw _jatw _j → 0 and the slopes of σ″_ij— σ′_ij curves for differentw _js [4] are employed to obtain τ_js. The former method is better in comparison to the existing one as it eliminates polar-polar interaction. The hf μ_js in Coulomb metre (C m) when compared with static and reported μs indicate that μ_s s favour the monomer formations which combine to form dimers in the hf electric field. The comparison among μs shows that a part of the molecule is rotating under X-band electric field [5]. The theoretical μ_theos from available bond angles and bond moments of the substituent polar groups attached to the parent molecules differ from the measured μ_js and μs to establish the possible existence of mesomeric, inductive and electromeric effects in polar liquid molecules.     

Electrical properties of amorphous (Co45Fe45Zr10)x(Al2O3)1?x nanocomposites

The electrical properties of (Co₄₅Fe₄₅Zr₁₀)_x(Al₂O₃)_1−x granular nanocomposites have been studied. The concentration dependences of electrical resistivity are S-shaped (in accordance with the percolation theory of conduction) with a threshold at a metallic component concentration of ∼41 at. %. An analysis of the temperature behavior carried out in the range 300–973 K revealed that structural relaxation and crystallization of the amorphous phase are accompanied by a decrease in the electrical resistivity of the composites above the percolation threshold and by its increase below the percolation threshold. For metallic phase concentrations x<41 at. %, variable range hopping conduction over localized states near the Fermi level was found to be dominant at low temperatures (77–180 K). A further increase in temperature brings about a crossover of the conduction mechanism from Mott’s law ln(σ) ∝ (1/T)^1/4 to ln(σ) ∝ (1/T)^1/2. A model of inelastic resonance tunneling over a chain of localized states of the dielectric matrix was used to find the average number of localized states involved in the charge transport between metallic grains. __________ Translated from Fizika Tverdogo Tela, Vol. 46, No. 11, 2004, pp. 2076–2082. Original Russian Text Copyright ? 2004 by Kalinin, Remizov, Sitnikov.     

Properties of superconducting Nb/Al/Nb/Al?AlOx?Al?AlOx?Al/Nb/Al/Nb tunnel junctions

Modified geometry (MG) devices, Nb/Al/Nb/Al−AlO_x−Al−AlO_x−Al/Nb/Al/Nb, have been fabricated and investigated in comparison with the basic geometry (BG) double-barrier Nb/Al−AlO_x−Al−AlO_x−Al/Nb devices. The enhancement of the critical temperature in the Al film is found to be weaker for the MG devices as compared with the BG devices at temperatures nearT=4.2 K but stronger at lowT. Indication of an enhancement of dc Josephson critical current density,j _c , at bias voltageV≠0 as compared withj _c (V=0) has been observed in the MG devices for the first time.     

Giant dielectric relaxation in SrTiO3-SrMg1/3Nb2/3O3 and SrTiO3-SrSc1/2Ta1/2O3 solid solutions

Ceramic samples of (1−x)SrTiO₃-xSrMg_1/3Nb_2/3O₃ and (1−x)SrTiO₃-xSrSc_1/2Ta_1/2O₃ were prepared, and their dielectric properties were studied at x=0.005–0.15 and 0.01–0.1, respectively, at frequencies 10 Hz–1 MHz and at temperatures 4.2–350 K. A giant dielectric relaxation was observed in the temperature range 150–300 K, and not so strong but well-developed relaxation was found in the temperature range 20–90 K. The activation energy U and the relaxation time τ₀ were determined to be 0.21–0.3 eV and from 10⁻¹¹ to 10⁻¹² s for the high-temperature relaxation and 0.01–0.02 eV and 10⁻⁸–10⁻¹⁰ s for the low-temperature relaxation, respectively. The additional local charge compensation of the heterovalent impurities Mg²⁺ and Nb⁵⁺ (or Sc³⁺ and Ta⁵⁺) by free charge carriers or the host ion vacancies is suggested to be the underlying physical mechanism of the relaxation phenomena. On the basis of this mechanism, the Maxwell-Wagner model and the model of reorienting dipole centers Mg²⁺ (or Sc³⁺) associated with the oxygen vacancy are proposed to explain the high-temperature relaxation with some arguments in favor of the latter model. The polaron-like model with the Nb⁵⁺-Ti³⁺ center is suggested as the origin of the low-temperature relaxation. The reasons for the absence of ferroelectric phase transitions in the solid solutions under study are also discussed. From Fizika Tverdogo Tela, Vol. 44, No. 11, 2002, pp. 1948–1957. Original English Text Copyright ? 2002 by Lemanov, Sotnikov, Smirnova, Weihnacht. This article was submitted by the authors in English.     

Absolute cross sections of electron attachment to molecular clusters. Part II: Formation of (H2O) N? , (N2O) N? , and (N2) N?

Absolute cross sections σ⁻(E, N) of electron attachment to clusters (H₂O) _N , (N₂O) _N , and (N₂) _N for varying electron energy E and cluster size N are measured by using crossed electron and cluster beams in a vacuum. Continua of σ⁻(E) are found that correlate well with the functions of electron impact excitation of molecules’ internal degrees of freedom. The electron is attached through its solvation in a cluster. In the formation of (H₂O) _N ⁻ , (N₂O) _N ⁻ , and (N₂) _N ⁻ , the curves σ⁻(N) have a well-defined threshold because of a rise in the electron thermalization and solvation probability with N. For (H₂O)₉₀₀, (N₂O)₃₅₀, and (N₂)₂₆₀ clusters at E = 0.2 eV, the energy losses by the slow electron in the cluster are estimated as 3.0 × 10⁷, 2.7 × 10⁷, and 6.0 × 10⁵ eV/m, respectively. It is found that the growth of σ⁻ with N is the fastest for (H₂O) _N and (N₂) _N clusters at E → 0 as a result of polarization capture of the s-electron. Specifically, at E = 0.1 eV and N = 260, σ⁻ = 3.0 × 10⁻¹³ cm² for H₂O clusters, 8.0 × 10⁻¹⁴ cm² for N₂O clusters, and 1.4 × 10⁻¹⁵ cm² for N₂ clusters; at E = 11 eV, σ⁻ = 9.0 × 10⁻¹⁶ cm² for (H₂O)₂₀₀ clusters, 2.4 × 10⁻¹⁴ cm² for (N₂O)₃₅₀ clusters, and 5.0 × 10⁻¹⁷ cm² for (N₂)₂₆₀ clusters; finally, at E = 30 eV, σ⁻ = 3.6 × 10⁻¹⁷ cm² for (N₂O)₁₀ clusters and 3.0 × 10⁻¹⁷ cm² for (N₂)₁₂₅ clusters. Original Russian Text ? A.A. Vostrikov, D.Yu. Dubov, 2006, published in Zhurnal Tekhnicheskoĭ Fiziki, 2006, Vol. 76, No. 12, pp. 1–15.     

The superconducting properties of YBa2(Cu1−xMx)3O7 for M=Zn and Ni

Transverse and zero-field μSR measurements were made on YBa₂(Cu_1−xNi_x)₃O_7−y withx=0.1 and 0.2, and YBa₂(Cu_1−x Zn _x )₃O_7−y withx=0.03, 0.06, 0.1, and 0.16, wherey≈0.1. Since doping may lead to magnetic ordering this was searched for with both zero and transverse field μSR, but no evidence was found over the temperature range studied: 10–100 K. However, depolarization rates as functions of temperature were obtained, and the low temperature values of these are σ=3.2 μs⁻¹.1.6μs⁻¹, and 1 μs⁻¹ forx=0.01, and 0.2 Ni, respectively, and σ=0.8 μs⁻¹, 0.75 μs⁻¹, 0.65 μs⁻¹, and 0.4 μs⁻¹ forx=0.03, 0.06, 0.1, and 0.16 Zn, respectively. Estimates for the effect of decreasing electron concentration for Zn are made, but these alone do not account for the drop in σ. Estimates for the effect of scattering on λ and hence σ are made. The reduction in σ for Ni dopant is in surprisingly good agreement with these estimates. For Zn the order of magnitude is correct, but the relative lack of further change in σ after the effect of the first 0.03 addition seems to imply a saturation of the effect of scattering.     

The Moduli of Flat PGL(2,ℝ) Connections on¶Riemann Surfaces

Suppose X is a compact Riemann surface with genus g>1. Each class [σ] ∈ Hom(π₁(X),PGL(2,ℝ))/PGL(2,ℝ) is associated with the first and second Stiefel–Whitney classes w ₁([σ]) and w ₂([σ]). The set of representation classes with a fixed w ₁≠ 0 has two connected components. These two connected components are characterized by w ₂ being 0 or 1. For each fixed w ₁≠ 0, we prove that the component, characterized by w ₂= 0, contains an open dense set diffeomorphic to the total space of a vector bundle of rank 2g−2 over a once punctured algebraic torus of dimension g−1. The other component, characterized by w ₂= 1, contains an open dense set diffeomorphic to the total space of a vector bundle of rank 2g−2 over an algebraic torus of dimension g−1. Received: 2 January 1997 / Accepted: 28 November 1998     

Observational constraint on generalized Chaplygin gas model

We investigate observational constraints on the generalized Chaplygin gas (GCG) model as the unification of dark matter and dark energy from the latest observational data: the Union SNe Ia data, the observational Hubble data, the SDSS baryon acoustic peak and the five-year WMAP shift parameter. The result is obtained that the best-fit values of the GCG model parameters with their confidence level are A _s=0.73_−0.06^+0.06 (1σ) _−0.09^+0.09 (2σ), α=−0.09_−0.12^+0.15 (1σ) _−0.19^+0.26 (2σ). Furthermore, in this model, we can see that the evolution of equation of state (EOS) for dark energy is similar to quiessence, and its current best-fit value is w _0de=−0.96 with the 1σ confidence level −0.91≥w _0de≥−1.00.     

Reciprocity relations for the effective electrical conductivity of randomly inhomogeneous media in the fractal regime

An exact relation for the realization-averaged effective conductivities in the fractal region is found for two-dimensional randomly inhomogeneous media. It has the form {σ _e (τ,L)~× {1/σ _e (−τ,L)~⁻¹=σ _e ² (τ=0, L≫ξ), where ξ is the correlation length (the self-averaging scale), L is the size of the system, τ=(p-p _c )/p _c , and p _c is the percolation threshold. For L≫ ξ, the system is self-averaged, and the relation transforms into the Dykhne reciprocity relation, A. M. Dykhne, Zh. éksp. Teor. Fiz. 59, 110 (1970) [Sov. Phys. JETP 32, 63 (1971)] σ _e (τ)σ _e (−τ])=σ _e ² (τ=0)= σ ₁ σ ₂. A similar relation is obtained for media with an exponentially broad distribution of local conductivities, as well as for individual realizations of some deterministic structures. Zh. éksp. Teor. Fiz. 113, 1484–1490 (April 1998)     

Spectrum of Non-Hermitian Heavy Tailed Random Matrices

Let (X _jk ) _j,k ≥ 1 be i.i.d. complex random variables such that |X _jk | is in the domain of attraction of an α-stable law, with 0 < α < 2. Our main result is a heavy tailed counterpart of Girko’s circular law. Namely, under some additional smoothness assumptions on the law of X _jk , we prove that there exist a deterministic sequence a _n ~ n ^1/α and a probability measure μ _α on \mathbbC{\mathbb{C}} depending only on α such that with probability one, the empirical distribution of the eigenvalues of the rescaled matrix (a_n^-1X_jk)_{1 ￡ j,k ￡ n}{(a_n^{-1}X_{jk})_{1\leq j,k\leq n}} converges weakly to μ _α as n → ∞. Our approach combines Aldous & Steele’s objective method with Girko’s Hermitization using logarithmic potentials. The underlying limiting object is defined on a bipartized version of Aldous’ Poisson Weighted Infinite Tree. Recursive relations on the tree provide some properties of μ _α . In contrast with the Hermitian case, we find that μ _α is not heavy tailed.     

The Behaviour of Aging Functions in One-Dimensional Bouchaud's Trap Model

Let τ_i be a collection of i.i.d. positive random variables with distribution in the domain of attraction of an α-stable law with α<1. The symmetric Bouchaud's trap model on ℤ is a Markov chain X(t) whose transition rates are given by w_xy=(2τ_x)⁻¹ if x, y are neighbours in ℤ. We study the behaviour of two correlation functions: ℙ[X(t_w+t)=X(t_w)] and It is well known that for any of these correlation functions a time-scale t=f(t_w) such that aging occurs can be found. We study these correlation functions on time-scales different from f(t_w), and we describe more precisely the behaviour of a singular diffusion obtained as the scaling limit of Bouchaud's trap model. Work supported by DFG Research Center Matheon ``Mathematics for key technologies'     

Indication of asymptotic scaling in the reactions dd → p3H, dd → n3He, and pd → pd

It is shown that the differential cross sections of the reactions dd → n ³He and dd → p ³H measured at a c.m.s. scattering angle θ_cm = 60° in the interval of the deuteron beam energy 0.5–1.2 GeV demonstrate the scaling behavior dσ/dt ∼ s ⁻²², which follows from constituent quark counting rules. It is found also that the differential cross section of the elastic dp → dp scattering at θ_cm = 125°–135° follows the scaling regime ∼s ⁻¹⁶ at beam energies 0.5–5 GeV. These data are parameterized here using the Reggeon exchange. From Pis’ma v Zhurnal éksperimental’noĭ i Teoreticheskoĭ Fiziki, Vol. 81, No. 7, 2005, pp. 387–390. Original English Text Copyright ? 2005 by Uzikov. This article was submitted by the author in English.     

Electrical relaxation in proton conductor composites based on (NH4)H2PO4/TiO2

We report on electrical relaxation measurements of (1 − x)NH₄H₂PO₄-xTiO₂ (x = 0.1) composites by admittance spectroscopy, in the 40-Hz–5-MHz frequency range and at temperatures between 303 and 563 K. Simultaneous thermal and electrical measurements on the composites identify a stable crystalline phase between 373 and 463 K. The real part of the conductivity, σ’, shows a power-law frequency dependence below 523 K, which is well described by Jonscher’s expression , where σ ₀ is the dc conductivity, ω _p /2π = f _p is a characteristic relaxation frequency, and n is a fractional exponent between 0 and 1. Both σ ₀ and f _p are thermally activated with nearly the same activation energy in the II region, indicating that the dispersive conductivity originates from the migration of protons. However, activation energies decrease from 0.55 to 0.35 eV and n increases toward 1.0, as the concentration of TiO₂ nanoparticles increases, thus, enhancing cooperative correlation among moving ions. The highest dc conductivity is obtained for the composite x = 0.05 concentration, with values above room temperature about three orders of magnitude higher than that of crystalline NH₄H₂PO₄ (ADP), reaching values on the order of 0.1 (Ω cm)^− 1 above 543 K.     

Temperature dependences of the high-field magnetization of dilute frustrated ferrimagnetic spinels

Results are presented of an investigation of the magnetic properties of dilute frustrated ferrimagnetic spinels Li_0.5Fe_2.5−x Ga_xO₄ (x=0.8–1.2), which characterize the main parameters of the ferrimagnetic state and provide evidence of local violation of collinear spin ordering and frustrations. In particular, measurements were made of the concentration dependences of the magnetic moment n ₀(x) and the Curie point T _c (x), the magnetization isotherms σ _T (H) at T=4.2 K and H⩽10 kOe, and also the low-and high-field magnetization polytherms σ _H (T). It was established that for x⩾0.8 in fields exceeding the technical saturation field H _s ∼2 kOe, the temperature dependences of the high-field magnetization σ _H (T) between 4.2 and 230 K cannot be described by the Bloch T ^3/2 law whereas this law is satisfied for undiluted Li spinel (x=0). Over the entire temperature range (4.2–230 K) the experimental curves σ _H (T) may be approximated by σ _H (T)=σ ₀(1−AT ^3/2 − BT ^5/2) for x=0.8–1.0 and σ _H (T)=σ ₀[1−CT ^3/2exp(μ(H−H ₀)/k _B T)] for x=1.1, 1.2, where μH ₀∼15 K is the internal field produced by competition between exchange interactions and frustrations. Fiz. Tverd. Tela (St. Petersburg) 40, 1075–1079 (June 1998)     

Effect of high pressure and chemical substitution on the crystal structure and magnetic state of R2Fe17 ? x Six (R = Lu or Y; x = 0 or 1.7)

The effect of high pressure on the crystal structure of the intermetallic compounds R₂Fe_{17 − x} Si_x (R = Lu or Y; x = 0 or 1.7) was studied using neutron diffraction. A correlation between changes in structural parameters and magnetic properties under the action of high pressure, as well as under chemical substitution of Si for Fe atoms, was analyzed in terms of localized moment and spin fluctuation models. The spin fluctuation model was found to describe more adequately the experimentally observed increase in the Curie temperature upon chemical substitution and the decrease in this temperature under the action of high pressure. Possible reasons for the suppression of a collinear ferromagnetic state and the occurrence of a noncollinear antiferromagnetic state in R₂Fe_17−x Si_x under pressure are discussed based on estimated differences between the total energy minima of these states. Original Russian Text ? D.P. Kozlenko, V.I. Voronin, V.P. Glazkov, B.N. Savenko, 2007, published in Pis’ma v Zhurnal éksperimental’noĭ i Teoreticheskoĭ Fiziki, 2007, Vol. 86, No. 9, pp. 675–680.     

Superconductivity and magnetic ordering in YBa2(Cu1−x Fe x )3O7

Transverse-and zero-field μSR measurements have been made for YBa₂(Cu_1−x Fe _x )₃O₇ withx=0.04, 0.08 and 0.12. The temperature range studied was from approximately 7.5 K to 100 K. The onset of magnetic ordering commences at about 7.5 K forx=0.04, 10 K forx=0.08 and 20 K forx=0.12. The Gaussian depolarization parameter, σ ofG _x (t) = exp(−σ² t ²/2), is depressed by a factor of about 0.6 forx=0.04, but for thex=0.08 sample σ is depressed by a factor of 10 and increasing suppression is seen as the temperature is lowered below 45 K. This decrease in σ is interpreted in terms of decreasing electronic mean free paths.