Bounds on the magnetic moment of the τ-neutrino via the process e~ e-→νγ

Using Breit-Wigner resonance relation, bounds on the magnetic moment of the tau-neutrino are calculated through the reaction e e-→νγ at the neutral boson pole in the framework of a superstring-inspired E6 model which has one extra low-energy neutral gauge boson and a LRSM.     

一种基于算法融合的红外目标跟踪方法

视频目标跟踪的难点在于快速、准确地在帧与帧之间匹配目标.由于红外图像目标与背景的反差低,图像的边缘模糊并且灰度级动态范围小,使红外目标跟踪难度比可见光更大.本文提出一种针对红外日标跟踪的融合算法,该方法融合直方图和不变矩的特点.首先利用目标的直方图计算简单快速的特点,由均值平移算法快速找到局部最优解,但由于该局部最优解仪为直方图匹配的最优解,缺少目标形状特征,与实际目标位置存在一定的偏差;其次,利用边缘小变矩作为修正特征修正误差,避免跟踪误差逐渐累计而最终导致跟踪失败,以提高跟踪的稳定性和精度.实验结果表明,该算法能够消除跟踪过程中的漂移现象,提高跟踪精度.     

Structured water chains in external electric fields

ABSTRACT

We study the structural, energetic and electronic properties of the structured water chain clusters within the density functional theory. We refer the structured water chains to those water clusters that have specific geometric patterns stretched along one direction. External electric field required to keep the structures open chain, thereby preventing them to form closed structures, is applied along the length of the chain. The structures are essentially periodic with basic repeating unit consisting of the corner- or edge-sharing 4-, 5- or 6-membered ring water clusters. Our calculations underscore the possible existence of such structured water clusters in the electrostatic environments, which we simulate in its simplicity employing a dipolar, uniform and static electric field. Analysis reveals that the 5-membered ring water chain clusters, i.e. the pentamer chain clusters have the lowest average dipole moment per water molecule while the threshold field, that marks the onset of the field-induced closure of the HOMO (highest occupied molecular orbital)-LUMO (lowest unoccupied molecular orbital) energy gap, is highest, followed by that for the tetramer and hexamer chains. The results suggest that the pentamer chains are the most stable clusters over a wide range of electric fields.     

Gas-phase 21Ne NMR studies and the nuclear magnetic dipole moment of neon-21

Gas-phase ²¹Ne nuclear magnetic resonance spectra were measured at the natural abundance of ²¹Ne isotope for samples consisting of pressurized neon up to 60 bar at room temperature and applying the magnetic field of the strength B₀ = 11.7574 T. It showed that the nuclear magnetic resonance frequency is linearly dependent on the density of gaseous neon. The resonance frequency was extrapolated to the zero-density point, and it permitted the determination of the ²¹Ne nuclear magnetic moment, μ(²¹Ne) = 0.6617774(10) μ_N. The present value of μ(²¹Ne) is not influenced by the bulk magnetic susceptibility of neon and interactions between neon atoms; therefore, it is more precise and reliable than the previous result obtained for μ(²¹Ne).     

Crystal field effects on the saturation magnetic moment of Sm3+ ion in ferronagnetic samarium compounds

The effects of cubic crystal fields on the saturation magnetic moment of Sm³⁺ ion in ferromagnetic compounds have been investigated. In samarium compounds with magnetic elements, the exchange fieldH _ex acting on Sm³⁺ ion is taken to be proportional to the sublattice magnetization of the magnetic element, while in compounds with nonmagnetic elementsH _ex is taken to be proportional to the spin average of the Sm³⁺ ion and is determined self-consistently. In both types of compoundsH _ex is assumed to be along [001] direction. The saturation magnetic moment is calculated by taking into account the admixture of excited (J=7/2 andJ=9/2) levels into the ground (J=5/2) level of Sm³⁺ ion by crystal fields and exchange fields. It is shown that depending upon the strength, the crystal fields quench or enhance the magnetic moment from the free ion value, and in some cases force Sm³⁺ ion to behave effectively like an (L+S) ion rather than an (L−S)ion. The crystal fields may have important bearing on the performance of samarium compounds as permanent magnet materials.     

A Canonical Compatible Metric for Geometric Structures on Nilmanifolds

Let (N, γ) be a nilpotent Lie group endowed with an invariant geometric structure (cf. symplectic, complex, hypercomplex or any of their ‘almost’ versions). We define a left invariant Riemannian metric on N compatible with γ to be minimal, if it minimizes the norm of the invariant part of the Ricci tensor among all compatible metrics with the same scalar curvature. We prove that minimal metrics (if any) are unique up to isometry and scaling, they develop soliton solutions for the ‘invariant Ricci’ flow and are characterized as the critical points of a natural variational problem. The uniqueness allows us to distinguish two geometric structures with Riemannian data, giving rise to a great deal of invariants.Our approach proposes to vary Lie brackets rather than inner products; our tool is the moment map for the action of a reductive Lie group on the algebraic variety of all Lie algebras, which we show to coincide in this setting with the Ricci operator. This gives us the possibility to use strong results from geometric invariant theory.Communicated by: Nigel Hitchin (Oxford) Mathematics Subject Classifications (2000): Primary: 53D05, 53D55; Secondary: 22E25, 53D20, 14L24, 53C30.     

Electronic structures and magnetic properties in SmCo7-xMx

The electronic structures and magnetic properties of SmCo7 xMx (M=Ti, Si, Zr, Hf, Cu, B, Ag, Ga, Mn) compounds are investigated by using a spin-polarized MS-X.α method. The results show that the long-range ferromagnetic order is determined by a stronger 3d-5d interaction, rather than the traditional RKKY interaction, and the effects of doping element M on 3d-5d coupling are negligible in Sm-Co-based compounds. The nonmagnetic dopant Si atoms have a larger effect on the moments of 2e site although they preferably occupy the Co 3g sites, which results in the stronger uniaxial anisotropy of this compound. Analysis of the formation energies indicates that 5d-element doped compounds are more stable than other dopants, and furthermore, they have a higher Curie temperature above room temperature, which will be in favor of their potential application as high-temperature permanent magnets.     

Molecular dynamics of polycrystalline cellobiose studied by solid-state NMR

Molecular motions of polycrystalline cellobiose have been investigated by measuring proton spin–lattice relaxation times, T₁ and T_1ρ, and the second moment, M₂, in both protonated and D₂O exchanged forms over the temperature range 120–380 K. T₁ relaxation is dominated by the motions of hydroxyl groups between 150 and 380 K, characterised by an activation energy of about 8.74 kJ/mol, whereas T_1ρ relaxation is driven by the motions of the same groups between 120 and 300 K. T_1ρ results suggest that hydroxyl groups have a distribution of dynamics. Motion of methylene groups was detected in the second-moment experiments at about 350 K, characterised by activation energy of about 40 kJ/mol. Consideration of the calculated and observed rigid-lattice second moments suggests that the reported X-ray data are incorrect for the inter-proton distance on C6′. ¹³C CPMAS spectra of both protonated and deuterated cellobiose have also been measured. Spectra of the deuterated material showed the existence of a second crystalline form in addition to the normal form.