Construction of Fredholm representations and a modification of the Higson-Roe corona

The Fredholm representation theory is well adapted to the construction of homotopy invariants of non-simply-connected manifolds by means of the generalized Hirzebruch formula [σ(M)] = 〈L(M)ch _A f*ξ, [M]〉 ∈ K _A ⁰(pt) ⊗ Q, where A = C*[π] is the C*-algebra of the group π, π = π ₁(M). The bundle ξ ∈ K _A ⁰(Bπ) is the canonical A-bundle generated by the natural representation π → A. Recently, the first author constructed a natural family of Fredholm representations that lead to a symmetric vector bundle on the completion of the fundamental group with a modification of the Higson-Roe corona, provided that the completion is a closed manifold.     

Formality Theorem for Hochschild Cochains via Transfer

We construct a 2-colored operad Ger _∞ which, on the one hand, extends the operad Ger _∞ governing homotopy Gerstenhaber algebras and, on the other hand, extends the 2-colored operad governing open-closed homotopy algebras. We show that Tamarkin’s Ger _∞-structure on the Hochschild cochain complex C ^•(A, A) of an A _∞-algebra A extends naturally to a Ger⁺_￥{{\bf Ger}^+_{\infty}}-structure on the pair (C ^•(A, A), A). We show that a formality quasi-isomorphism for the Hochschild cochains of the polynomial algebra can be obtained via transfer of this Ger⁺_￥{{\bf Ger}^+_{\infty}}-structure to the cohomology of the pair (C ^•(A, A), A). We show that Ger⁺_￥{{\bf Ger}^+_{\infty}} is a sub DG operad of the first sheet E ¹(SC) of the homology spectral sequence for the Fulton–MacPherson version SC of Voronov’s Swiss Cheese operad. Finally, we prove that the DG operads Ger⁺_￥{{\bf Ger}^+_{\infty}} and E ¹(SC) are non-formal.     

Eigenvalues of Laplacian with Constant Magnetic Field on Non-Compact Hyperbolic Surfaces with Finite Area

We consider a magnetic Laplacian −Δ _A = (id + A)^* (id + A) on a non-compact hyperbolic surface M with finite area. A is a real one-form and the magnetic field dA is constant in each cusp. When the harmonic component of A satisfies some quantified condition, the spectrum of −Δ _A is discrete. In this case, we prove that the counting function of the eigenvalues of −Δ _A satisfies the classical Weyl formula, even when dA=0.     

A<Subscript>4</Subscript> symmetry and lepton masses and mixing

Stimulated by Ma’s idea, which explains the tribimaximal neutrino mixing by assuming an A₄ flavor symmetry, a lepton mass matrix model is investigated. A Frogatt–Nielsen-type model is assumed, and the flavor structures of the masses and mixing are caused by the VEVs of SU(2)_L singlet scalars φ_i ^u and φ_i ^d (i=1,2,3), which are assigned to 3 and (1 ,1 ’,1 ”) of A₄, respectively. Possible charged lepton and neutrino mass spectra and mixing are investigated.     

The thermodynamics of energy-storing photoprocesess

A solution is found for the most general formulation of the problem of the thermodynamic limitations on the rate of increase of the free energy of a closed photochemical system interacting with a heat bath and a radiation field. A reaction of the form A ₁ ^* +A ₂→A ₃+A ₄ is used to compare the thermodynamically maximum energy yield of the process of storing radiant energy with the “kinetic” limit of the same quantity. Zh. Tekh. Fiz. 67, 54–58 (June 1997)     

Spontaneous emission in dielectric nanoparticles

An analytical expression is obtained for the radiative-decay rate of an excited optical center in an ellipsoidal dielectric nanoparticle (with sizes much less than the wavelength) surrounded by a dielectric medium. It is found that the ratio of the decay rate A _nano of an excited optical center in the nanoparticle to the decay rate A _bulk of an excited optical center in the bulk sample is independent of the local-field correction and, therefore, of the adopted local-field model. Moreover, the expression implies that the ratio A _nano/A _bulk for oblate and prolate ellipsoids depends strongly on the orientation of the dipole moment of the transition with respect to the ellipsoid axes. In the case of spherical nanoparticles, a formula relating the decay rate A _nano and the dielectric parameters of the nanocomposite and the volumetric content c of these particles in the nanocomposite is derived. This formula reduces to a known expression for spherical nanoparticles in the limit c ≪ 1, while the ratio A _nano/A _bulk approaches unity as c tends to unity. The analysis shows that the approach used in a number of papers {H. P. Christensen, D. R. Gabbe, and H. P. Jenssen, Phys. Rev. B 25, 1467 (1982); R. S. Meltzer, S. P. Feofilov, B. Tissue, and H. B. Yuan, Phys. Rev. B 60, R14012 (1999); R. I. Zakharchenya, A. A. Kaplyanskii, A. B. Kulinkin, et al., Fiz. Tverd. Tela 45, 2104 (2003) [Phys. Solid State 45, 2209 (2003)]; G. Manoj Kumar, D. Narayana Rao, and G. S. Agarwal, Phys. Rev. Lett. 91, 203903 (2003); Chang-Kui Duan, Michael F. Reid, and Zhongqing Wang, Phys. Lett. A 343, 474 (2005); K. Dolgaleva, R. W. Boyd, and P. W. Milonni, J. Opt. Soc. Am. B 24, 516 (2007)}, for which the formula for A _nano is derived merely by substituting the bulk refractive index by the effective refractive index of the nanocomposite must be revised, because the resulting ratio A _nano/A _bulk turns out to depend on the local-field model. The formulas for the emission and absorption cross sections σ_nano for nanoparticles are derived. It is shown that the ratios σ_nano/σ_bulk and A _nano/A _bulk are not equal in general, which can be used to improve the lasing parameters. The experimentally determined and theoretically evaluated decay times of metastable states of dopant rare-earth ions in crystalline YAG and Y₂O₃ nanoparticles are compared with the corresponding values for bulk crystals of the same structure. Original Russian Text ? K.K. Pukhov, T.T. Basiev, Yu.V. Orlovskii, 2008, published in Pis’ma v Zhurnal éksperimental’noĭ i Teoreticheskoĭ Fiziki, 2008, Vol. 88, No. 1, pp. 14–20.     

Dirac Operators Coupled to the Quantized Radiation Field: Essential Self-adjointness à la Chernoff

We study the Dirac operator D ₀ in an external potential V, coupled to a quantized radiation field with energy H _f and vector potential A. Our result is a Chernoff-type theorem, i.e., we prove, for the operator D ₀+α · A+V +λ H _f with λ ∈{0, 1}, that the essential self-adjointness is not affected by the behavior of V at ∞.      

Determination of the neutron electric form factor from the reaction 3 He(e,e'n) at medium momentum transfer

The electric form factor of the neutron G_En has been determined in double polarized exclusive ³ He(e,e'n) scattering in quasi–elastic kinematics by measuring asymmetries A _⊥, A _∥ of the cross section with respect to helicity reversal of the electron, with the nuclear spin being oriented perpendicular to the momentum transfer q in case of A_⊥ and parallel in case of A_∥. The experiment was performed at the 855 MeV c. w. microtron MAMI at Mainz. The degree of polarization of the electron beam and of the gaseous ³ He target were each about 50%. Scattered electrons and neutrons were detected in coincidence by detector arrays covering large solid angles. Quasi–elastic scattering events were reconstructed from the measured electron scattering angles ϑ_e, φ_e and the neutron momentum vector p _n ^′ in the plane wave impulse approximation. We obtain the result <G _En>_{(0.27 < Q2c2/GeV2 < 0.5)}= 0.0334 ± 0.0033_stat± 0.0028_syst which is averaged over the indicated range of Q ², the squared momentum transfer. This G _En value is significantly smaller than measured from the D(e,e'n) reaction under similar kinematical conditions. To what extent final state interactions in ³He quench the G _En result is subject of calculations currently in progress elsewhere. Received: 29 April 1999     

Magnetically induced spatial dispersion in the cubic magnetic semiconductors Cd1−x MnxTe

In the transverse geometry we have detected birefringence that is linear in the magnetic field B and the light wave vector k in the cubic magnetic semiconductors Cd_1−x Mn_xTe (0⩽x⩽0.52). The effect was found to be large, ∼1 (deg cm⁻¹ T⁻¹), and highly anisotropic, in contrast to the Faraday and Voigt effects. The phenomenon is represented by terms of type γ _ijklB_kk_l in the permittivity tensor ε _ij and can be described by two parameters, A and g. Spectral studies have shown that the normalized parameters A/x and g/x are independent of x, i.e., the effect can be related to the Mn²⁺ ions. Below the edge E _g of the forbidden band, the dispersion of A is described by a (E _g−E)^−1.4-dependence, while the dispersion of g is nil. Theoretical analysis has shown that the spectral curves for A and g can be explained by the special features of the dispersion laws for electrons and holes (features related to the fact that there is no inversion center) and by the dependence of the parameters of the exchange interaction on the electron wave vector. Zh. éksp. Teor. Fiz. 114, 1018–1033 (September 1998)     

Swelling of two-dimensional polymer rings by trapped particles

The mean area of a two-dimensional Gaussian ring of N monomers is known to diverge when the ring is subject to a critical pressure differential, p _c ∼ N ^-1. In a recent publication (Eur. Phys. J. E 19, 461 (2006)) we have shown that for an inextensible freely jointed ring this divergence turns into a second-order transition from a crumpled state, where the mean area scales as 〈A〉 ∼ N, to a smooth state with 〈A〉 ∼ N ². In the current work we extend these two models to the case where the swelling of the ring is caused by trapped ideal-gas particles. The Gaussian model is solved exactly, and the freely jointed one is treated using a Flory argument, mean-field theory, and Monte Carlo simulations. For a fixed number Q of trapped particles the criticality disappears in both models through an unusual mechanism, arising from the absence of an area constraint. In the Gaussian case the ring swells to such a mean area, 〈A〉 ∼ NQ, that the pressure exerted by the particles is at p _c for any Q. In the freely jointed model the mean area is such that the particle pressure is always higher than p _c, and 〈A〉 consequently follows a single scaling law, 〈A〉 ∼ N ² f (Q/N), for any Q. By contrast, when the particles are in contact with a reservoir of fixed chemical potential, the criticality is retained. Thus, the two ensembles are manifestly inequivalent in these systems. An erratum to this article is available at .     

HPLC-based activity profiling for GABA<Subscript>A</Subscript> receptor modulators from the traditional Chinese herbal drug Kushen (<Emphasis Type="Italic">Sophora flavescens</Emphasis> root)

An EtOAc extract from the roots of Sophora flavescens (Kushen) potentiated γ-aminobutyric acid (GABA)-induced chloride influx in Xenopus oocytes transiently expressing GABA_A receptors with subunit composition, α ₁ β ₂ γ _2S. HPLC-based activity profiling of the extract led to the identification of 8-lavandulyl flavonoids, kushenol I, sophoraflavanone G, (−)-kurarinone, and kuraridine as GABA_A receptor modulators. In addition, a series of inactive structurally related flavonoids were characterized. Among these, kushenol Y (4) was identified as a new natural product. The 8-lavandulyl flavonoids are first representatives of a novel scaffold for the target.     

ESR of V4+ in α-RbTiOPO4 single crystals

We have recorded and investigated the ESR spectrum of vanadium-doped α-RbTiOPO₄ single crystals in the temperature interval 77–300 K. Two types of structurally distinct centers, V1 and V2, with a 4:1 ratio of the peak intensities were observed. The angular dependences of the resonance magnetic fields are described by a spin Hamiltonian corresponding to axial symmetry with the parameters g _∥1=1.9305, g _⊥1=1.9565, A _∥1=−168.2×10⁻⁴cm⁻¹, and A _⊥1=−54.3×10⁻⁴cm⁻¹ for V1 centers and g _∥2=1.9340, g _⊥2=1.9523, A _∥2=−169.0×10⁻⁴cm⁻¹, and A _⊥2=−55.2×10⁻⁴cm⁻¹ for V2 centers. A model of a paramagnetic center is proposed: The vanadium ions replace titanium ions in two structurally distinct positions Ti1 and Ti2 (V1 and V2 centers, respectively). The possibility that a VO²⁺ ion forms when α-RbTiOPO₄ crystals and crystals of the KTP group (KTiOPO₄, NaTiOPO₄, α-and β-LiTiOPO₄), studied earlier, are doped with vanadium is discussed. Fiz. Tverd. Tela (St. Petersburg) 40, 534–536 (March 1998)     

Comment: “On the computation of molecular auxiliary functions<Emphasis Type="Italic">A</Emphasis><Subscript>n</Subscript>and<Emphasis Type="Italic">B</Emphasis><Subscript>n</Subscript>”

Guseinov, Mamedov, Kara and Orbay (Pramana - J. Phys. 56, 691 (2001)) propose methods for evaluating the molecular auxiliary functionsA _n(p) andB _n(pt) for the range 17 ≤n ≤ 60 and 25 ≤pt ≤ 60. However, their procedure forA _n(p) is not new, and that forB _n(pt) is less efficient for their target range than another well-known method. Their approach does have merit for smaller non-zero values ofpt. Two minor errors in table 1 of their paper are also identified.     

Classes on Compactifications of the Moduli Space of Curves Through Solutions to the Quantum Master Equation

In this paper we describe a construction which produces classes in compactifications of the moduli space of curves. This construction extends a construction of Kontsevich which produces classes in the open moduli space from the initial data of a cyclic A _∞-algebra. The initial data for our construction are what we call a ‘quantum A _∞-algebra’, which arises as a type of deformation of a cyclic A _∞-algebra. The deformation theory for these structures is described explicitly. We construct a family of examples of quantum A _∞-algebras which extend a family of cyclic A _∞-algebras, introduced by Kontsevich, which are known to produce all the kappa classes using his construction.      

A Statistical Mechanics Approach for a Rigidity Problem

We focus the problem of establishing when a statistical mechanics system is determined by its free energy. A lattice system, modelled by a directed and weighted graph (whose vertices are the spins and its adjacency matrix M will be given by the system transition rules), is considered. For a matrix A(q), depending on the system interactions, with entries which are in the ring Z[a ^q :a∈R ⁺] and such that A(0) equals the integral matrix M, the system free energy β _A (q) will be defined as the spectral radius of A(q). This kind of free energy will be related with that normally introduced in Statistical Mechanics as proportional to the logarithm of the partition function. Then we analyze under what conditions the following statement could be valid: if two systems have respectively matrices A,B and β _A = β _B then the matrices are equivalent in some sense. Issues of this nature receive the name of rigidity problems. Our scheme, for finite interactions, closely follows that developed, within a dynamical context, by Pollicott and Weiss but now emphasizing their statistical mechanics aspects and including a classification for Gibbs states associated to matrices A(q). Since this procedure is not applicable for infinite range interactions, we discuss a way to obtain also some rigidity results for long range potentials.     

Anisotropic impurity scattering in palladium silver alloys

Measurements have been made of the Hall coefficientR of some alloys of silver in palladium over the temperature range 1°K to 120°K. The alloys contain between ∼1 and ∼10 at.-% silver. Values ofR were also obtained at room temperature and these were in good agreement with earlier published work. The values ofR are negative in all the alloys, and |R| increases both on reducing the temperature and increasing the silver concentration,c. Below ∼10°K, |R| becomes independent of temperature but shows a linear dependence onc, increasing by a factor of 2.5 over the concentration range measured. This increase is too great to be accounted for in terms of band structure changes alone, so we have examined the effects of anisotropic impurity scattering. To a first approximation it can be shown thatR is proportional to an anisotropy parameterA, defined asA=〈τ ²(k)〉/〈τ(k)〉², whereτ(k) represents the relaxation time of an electron in a statek, and 〈〉 is an average over the Fermi surface. In palladium we assume that the majority of the current is carried by the s-electrons. In the presence of silver impurities these electrons can be scattered into s-states or d-states with relaxation times given byτ _ss α1/c(1−c) andτ _sd α1/c ²(1−c) respectively. FollowingPlate we have assumed thatτ _ss is isotropic and thatτ _sd is anisotropic, leading to an overall anisotropic relaxation time for impurity scattering. We then find the parameterA increases approximately linearly with silver content, in accordance with our experimental results.     

Interaction force between incompatible star-polymers in dilute solution

We consider a low-density assembly of spherical colloids, such that each is clothed by L end-grafted chemically incompatible polymer chains either of types A or B. These are assumed to be dissolved in a good common solvent. We assume that colloids are of small size to be considered as star-polymers. Two adjacent star-polymers A and B interact through a force F originating from both excluded-volume effects and chemical mismatch between unlike monomers. Using a method developed by Witten and Pincus (Macromolecules 19, 2509 (1986)) in the context of star-polymers of the same chemical nature, we determine exactly the force F as a function of the center-to-center distance h. We find that this force is the sum of two contributions F _e and F _s. The former, that results from the excluded volume, decays as F _e∼A _L h ^-1, with the L -dependent universal amplitude A _L∼L ^3/2. While the second, which comes from the chemical mismatch, decays more slowly as F _s∼χB _L h ^{-1 - τ}, where τ is a critical exponent whose value is found to be τ 0.40, and χ is the standard Flory interaction parameter. We find that the corresponding L-dependent universal amplitude is B _L∼L ^{3 + τ /2}. Theses forces are comparable near the cores of two adjacent star-polymers, i.e. for h∼h _c∼a (a is the monomer size). Finally, for two star-polymers of the same chemical nature (A or B), the force F that simply results from excluded-volume effects coincides exactly with F _e, and then the known result is recovered. Received 2 October 2000 and Received in final form 24 January 2001     

Partial Dynamical Systems and the KMS Condition

 Given a countably infinite 0–1 matrix A without identically zero rows, let 𝒪 _A be the Cuntz–Krieger algebra recently introduced by the authors and 𝒯 _A be the Toeplitz extension of 𝒪 _A , once the latter is seen as a Cuntz–Pimsner algebra, as recently shown by Szymański. We study the KMS equilibrium states of C ^* -dynamical systems based on 𝒪 _A and 𝒯 _A , with dynamics satisfying for the canonical generating partial isometries s _x and arbitrary real numbers N _x > 1. The KMS_β states on both 𝒪 _A and 𝒯 _A are completely characterized for certain values of the inverse temperature β, according to the position of β relative to three critical values, defined to be the abscissa of convergence of certain Dirichlet series associated to A and the N(x). Our results for 𝒪 _A are derived from those for 𝒯 _A by virtue of the former being a covariant quotient of the latter. When the matrix A is finite, these results give theorems of Olesen and Pedersen for 𝒪 _n and of Enomoto, Fujii and Watatani for 𝒪 _A as particular cases. Received: 21 November 2000 / Accepted: 31 May 2002 Published online: 22 November 2002 RID="*" ID="*" Partially supported by CNP_q RID="**, ***"     

EPR of trivalent iron ions in a LiCaAlF6 crystal

The orientational dependences of the EPR spectra of Fe³⁺-doped LiCaAlF₆ single crystals (space group P31c, Z=2), grown at the Laboratory of Magnetic Radio Spectroscopy at Kazan’ State University, have been investigated in detail. The spectrum is described by a trigonal spin Hamiltonian with the following parameters: B ₂₀=40.072×10⁻⁴ cm⁻¹, B ₄₀=−5.799×10⁻⁴ cm⁻¹, B ₄₃=−4.281×10⁻⁴ cm⁻¹, A _s=24.33±1, A _p=6.13±1, g _∥=g _⊥=2.00217±0.0003. A theoretical calculation of the hyperfine structure parameters shows that they are described quite well when allowance is made for the overlapping of the wave functions of the paramagnetic center and the ligands (F⁻). Fiz. Tverd. Tela (St. Petersburg) 39, 488–490 (March 1997)