Quadrupole moments of medium-weight and heavy hypernuclei with the NΛ configurations (N = p and n)

Using the shell model wave functions, we have studied quadrupole moments of medium-weight and heavy hypernuclei, and obtained the shell model values of quadrupole moments of NΛ systems ( N = p and n). With the use of the first-order perturbation theory, we have also estimated the configuration mixing effects on quadrupole moments of these NΛ hypernuclei. We show that the hyperon-induced configuration mixing effects are small and the nucleon-induced configuration mixing effects are large in many cases. Received: 22 February 2000 / Accepted: 2 August 2000     

New algebraic solutions for SO(6) ↔ U(5) transitional nuclei in the interacting boson model

Exact solutions for energy eigenvalues and eigenstates for SO(6) ↔ U(5) transitional (Class C) nuclei in IBM-1 and one case in IBM-2 are found by using an infinite dimensional algebraic method. As examples, the energy spectra and some E2 transition rates and quadrupole moments of the ^100–108Ru and ^102–112Pd isotopes are calculated in IBM-1 and compared with experimental results.     

He-broadening and shifting coefficients of HCl lines in the (1←0) and (2←0) infrared transitions

ABSTRACT

We report experimental results on the broadening and shifting coefficients in a large interval of J quantum numbers in the fundamental and first overtone vibration–rotation bands of the HCl molecule in mixtures with helium. Many of the values, especially for the overtone transition, are novel. The uncertainties for the isotope-averaged broadening coefficients amount to 2% on average for the fundamental and 1.5% for the overtone bands. Shifts have a typical uncertainty of 3%.     

Extrapolation of theS(E) factor in7Be(p, γ0)8B: the7Li(p, γ0)8Be case

The observed M1 capture amplitude in⁷Li(p,_o)⁸Be At E_p=80–0 keV originates predominantly from the low-energy tail of a resonance at 441 keV, thue removing a recent criticism on the extrapolation of S(E) data such as for⁷Be(p,)⁸B.     

Precision (n, γ)-measurements of high energy transitions in the nuclei198Au and199Au

On the IRIS facility the new neutron deficient ^{157,158,160,161,163}Lu isotopes have been produced in spallation induced by 1 GeV protons on a tungsten or tantalum target, and identified by mass separation and the subsequent decay spectroscopy (X-, gamma-, and alpha ray spectroscopy).     

The E1 and E2 capture amplitudes in 12C(α,γ0)16O

Excitation functions of the %₀ capture transition in ¹²C(!,%)¹⁶O at /_% = 90^§ were obtained using a 4 2 4' BGO crystal in close geometry (E = 0.94 to 3.39 MeV) and a 2 2 2' BGO crystal in far geometry (E = 1.69 to 3.29 MeV), where the study of the reaction was initiated in inverse kinematics involving a windowless gas target. The small crystal detected essentially the E1 multipole component in the %₀ capture transition, while the large crystal observed approximately the angle-integrated sum of the E1 and E2 multipole components. Analysis of the two data sets together with data from previous work provided strong evidence that both multipoles are of equal importance at the relevant stellar energy E₀ = 0.3 MeV.     

Variation in the Luminescence Lifetimes of Eucl3·nH2O(N=0,L,2,3,6)

Eu³⁺ ion emission spectra and luminescence lifetimes were investigated for EuCl₃ -nH₂O (n=0,1,2,3,6). Each compound exhibited a characteristic set of emission bands and a specific luminescence lifetime. The number of water molecules and chloride ions coordinated to the Eu³⁺ ion in these materials was estimated from the observed lifetimes, spectroscopic implications, and expected lanthanide coordination numbers. Approximation of the observed luminescence decay constant for each material was possible through the use of arithmetic terms associated with both the complexed water molecules and the complexed chloride ions which make up the inner-coordination sphere of the Eu³⁺ ion.     

A contribution from collective rotation to ΔI=±1 transitions in the cranking model

The contribution of the orientational polarization of the core to quasiparticle transition amplitudes in deformed nuclei is derived. In the cranked mean-field model, these contributions arise from the coupling of rotational RPA excitations to the quasiparticles. They reduced to the usual core contribution (g_R) for M1 transitions, and give a collective and possibly oscillatory contribution to E2 transitions with ΔI=±1.     

The S(E) factor of7Li(p, γ)8Be and consequences for S(E) extrapolation in7Be(p, γ0)8B

Excitation functions and forward-backward anisotropies have been measured for the⁷Li(p, )⁸Be capture reaction over the proton energy rangeE _p =100 to 1500 keV, using a 4 summing crystal and Ge(Li) detectors, respectively. The data show at all energies the presence of El and M1 capture amplitudes arising from the direct capture (DC) process and theE _R =441 and 1030 keV resonances, respectively. Due to the observed DC process, the present data increase significantly the reaction rates (up to a factor of 110) compared to values given in the compilation. The data and their analyses remove the recent criticism on DC model calculations, which had implied a significant reduction in the extrapolated S(E) factor for⁷Be(p,)B and thus in the predicted flux of high-energy solar neutrinos; thus, the solar neutrino problem is still with us.Supported in part by the Deutsche Forschungsgemeinschaft (Ro429/21-3 and Ro429/21-4) and the German-Hungarian Collaboration (X238.6 and OTKA3808)     

Temperature hysteresis of magnetic phase transitions in Tb1 − x Ce x Mn2O5 (x = 0, 0.20, 0.25)

The temperature evolution of the magnetic structure of multiferroics Tb_{1 ? x} Ce _x Mn₂O₅ (x = 0, 0.20, 0.25) has been investigated using the neutron scattering methods. It has been found that, despite the qualitative similarity of the magnetic states and the series of phase transitions for pure TbMn₂O₅ (TMO) and doped crystals Tb_{1 ? x} Ce _x Mn₂O₅ (TCMO, x = 0.20 and 0.25), there are significant differences in their properties. In contrast to TMO, where there are three magnetic phases, TCMO can include two magnetic phases that coexist in a wide temperature range and exhibit a rather wide temperature hysteresis. One of these phases with wave vector k ₁ = (0.5, 0, k _z1), k _z1 = 0.25, is commensurate and arises at temperatures below T _N ～ 39 K (for x = 0.2) and T _N ～ 38 K (x = 0.25). The second phase is incommensurate with wave vector k ₂ = (1/2, 0, k _z2), k _z2 = 0.256(2), and appears upon cooling at T = 21 K (x = 0.2) and T = 19 K (x = 0.25). Upon further cooling to 16 K, the component k _z2 increases to 0.292(2) and then remains constant. The component k _z1 increases to the value of 0.280(2) upon cooling in the range from 15 to 10 K and then remains constant down to 1.5 K. With an increase in the temperature, the components k _z1 and k _z2 undergo reverse changes to their initial values, but these changes occur at temperatures 7 K higher than those observed with a decrease in the temperature. For TMO, two phases also coexist, but the temperature hysteresis in this case is considerably smaller than for TCMO. This is explained by different densities of domain walls and different sizes of domains in pure and doped crystals.     

Imperfection of the clustered perovskite structure, phase transitions, and magnetoresistive properties of ceramic La0.6Sr0.2Mn1.2 ? x Ni x O3 ± δ (x = 0–0.3)

Ceramic samples of lanthanum strontium manganite perovskites La_0.6Sr_0.2Mn_{1.2 ? x} Ni _x O_{3 ± ??} (0 ?? x ?? 0.3) have been investigated using the X-ray diffraction, magnetic (??_ac), ⁵⁵Mn NMR, resistive, and magnetoresistive methods. The specific features of the influence of the composition on the structure and properties of nonstoichiometric manganite perovskites have been established. It has been found that the rhombohedrally (R $\bar 3$ c) distorted perovskite structure contains cation and anion vacancies, as well as nanostructured clusters with Mn²⁺ ions in the A-positions. The substitution of Ni³⁺ ions (r = 0.74 ?) for Mn³⁺ ions (r = 0.785 ?) leads to a decrease in the lattice parameter a, the ferromagnetic-paramagnetic phase transition temperature T _C, and the metal-semiconductor phase transition temperature T _ms due to the disturbance of the superexchange interactions between heterovalent manganese ions Mn³⁺ and Mn⁴⁺. The observed anomalous magnetic hysteresis at 77 K has been explained by the antiferromagnetic effect of the unidirectional exchange anisotropy of the ferromagnetic matrix structure on the magnetic moments of the superstoichiometric manganese Mn²⁺ ions located in nanostructured planar clusters. An analysis of the asymmetrically broadened ⁵⁵Mn NMR spectra of the compounds has revealed a high-frequency electronic superexchange of the ions Mn³⁺ ? O^2? ? Mn⁴⁺; a local heterogeneity of their surrounding by other ions, vacancies, and clusters; and a partial localization of Mn⁴⁺ ions. The local hyperfine interaction fields on ⁵⁵Mn nuclei have been determined. The concentration dependences of the activation energy and charge hopping frequency have confirmed that the Ni ions decrease the electrical conductivity due to the weakening of the electronic superexchange Mn³⁺ ? O^2? ? Mn⁴⁺. Two types of magnetoresistive effects have been found: one effect, which is observed near the phase transition temperatures T _C and T _ms, is caused by scattering at intracrystalline nanostructured heterogeneities, and the other effect, which is observed in the low-temperature range, is induced by tunneling through intercrystalline mesostructured boundaries. The phase diagram has demonstrated that there is a strong correlation between magnetic and electrical properties in rare-earth manganites.     

Correlation of the magnetic and transport properties with polymorphic transitions in bismuth pyrostannate Bi2(Sn1 − x Cr x )2O7

Physics of the Solid State - The correlation of the electrical, magnetic, and structural properties of Bi2(Sn1 − x Cr x )2O7 solid solutions has been investigated for two compositions with x...     

Dynamical symmetry breaking in an SU(2)⊗U(1) model with two right singlets and gauge boson masses

A four-fermion interaction which includes right singlets of both up and down fermions is included in the initial locally SU(2)S(1)-invariant model. In the suitable approximation, the propagators are constructed and the mass spectrum is found of fermi and gauge vector fields as well as of the collective scalar fields due to the dynamical symmetry breakdown.Translated from Izvestiya Uchebnykh Zavedenii, Fizika, No. 4, pp. 98–104, April, 1990.     

The S21 lines of the A2Σ+ (v′ = 1)←X2Π (v″ = 0) transitions of OH and OD

The S₂₁ lines of the OH radical for the A²Σ⁺ (v′ = 1)←X²Π (v″ = 0) transition have been observed in the 278–280 nm region from the laser-excitation spectrum. The OH radical was generated from either the H + NO₂ or the H + O₃ reaction in a flow system and the fluorescence passing through a 309.6 nm interference filter was detected with a photomultiplier-boxcar integrator arrangement. The weak S₂₁ lines were observed at laser energies above 0.2 mJ. The observed peak wavenumbers are in excellent agreement with those predicted for the S₂₁ bands of the A (v>′ = 1)←X (v″ = 0) transition from the known spectroscopic parameters. Observation of the corresponding S₂₁ system for OD in the 286.0–286.9 nm region further confirms this assignment. The relative absorption cross-sections of about one-tenth those of the P₁ lines are in good agreement with theoretical considerations.     

羟基水团簇OH~n(H_2O)_3(n=0,±1)的比较研究

使用粒子群优化算法结合从头算方法得到了羟基水团簇OH~n(H_2O)_3(n=0,±1)的低能结构,并对考虑零点能后最稳定的团簇的成键、分子轨道和红外性质进行了对比研究.对最高占据轨道进行键序分析表明:阴离子团簇中的外来电子占据了羟基中的氧原子的空轨道,自由基型团簇中的部分电子从水分子转移到了羟基上,阳离子团簇中形成了很强的氧氧键.对这些团簇的红外谱进行了计算和分析,这将为相关实验提供理论参考.