可能的qQ■，qq■■和qQ■■重四夸克态(英文)

假设X(3872)是一个qc(?)四夸克态,并用它的质量作为输入,用具有味对称性破坏的色磁相互作用系统研究了可能的重四夸克态的质量谱．     

多夸克态研究简述

介绍了多夸克态的研究现状. 主要介绍了四夸克态、五夸克态和双重子态的理论研究. 并列举了实验上观察到的可能是多夸克态的粒子或共振态.     

Jaffe与Wilczek双夸克模型中的负宇称五夸克态

如果Jaffe与Wilczek关于Q5+五夸克态的双夸克图像是正确的话,那就应该存在负宇称的五夸克SU(3)八重态与单态,其中两个双夸克间没有轨道激发.这些态比Q5+质量低,与传统夸克模型中的由三夸克构成的重子的轨道激发质量接近.我们计算了这些负宇称态的质量与磁矩,用手征有效拉氏量讨论了他们可能的强衰变模式和选择定择，发现有两个态可能比较窄.我们建议实验上寻找这九个额外的负宇称态.如果将来的实验确实发现了这些态,那是对Jaffe与Wilczek双夸克模型的直接验证.否则,应该重新评估Jaffe与Wilczek的双夸克图像甚至抛弃这个模型.     

手征夸克模型下ud四夸克态的研究(英文)

在手征SU(3)夸克模型和扩展的手征SU(3)夸克模型的框架下,用变分的方法系统地研究了同位旋为0、1,自旋宇称为0~ 、1~ 和2~ 的ud■四夸克系统6个低组态的能量.模型的参数取自以前的工作,它能很好地描述核子-核子散射相移以及核子-超子散射截面.S道相互作用的参数由拟合K介子和K~*介子的质量定出,并且考虑了具有相同量子数的态之间的态混合效应.结果表明,同位旋为0且自旋宇称为1~ 的ud■能量低于相应的K~*K~*的阈能,且该组态中KK~*的成分相当小,因此该组态的宽度可能较小,可视为一个可能的四夸克态的候选者.     

原子核内的夸克效应

这篇评述文章说明了下面四个问题:(i)任何色单态夸克反夸克系统的隐色道一定可以用通常的强子道表示出来,因此任何与隐色道有关的物理总可以用通常的强子自由度来解释;(ii)夸克胶子交换和矢量介子交换产生的重子重子自旋轨道耦合力非常相似,因此不能指望用超核的自旋轨道劈裂来区别夸克胶子交换模型和矢量介子交换模型;(iii)对于破坏电荷独立及电荷对称的重子互作用,电磁作用和夸克质量差同样重要,任何电荷相关互作用的计算必须同时考虑电磁作用和夸克质量差;(iV)和QED中的电子脱局域效应相似,我们猜测对QCD可能有夸克脱囚禁效应并且研究了此效应在双重子系统中的表现。     

重夸克等效理论和重味强子体系质量谱的研究

利用重夸克等数理论,对重味强子Qq、QQq和Qqq以及四夸克态QQqq的质量谱进行了系统定性的研究,并与势模型对QQqq的计算结果进行了比较.     

五夸克态Θ的手征夸克模型研究(英文)

在手征夸克模型的框架下, 研究了五夸克态 uudd的结构. 分别考虑了 Jπ=(1/2)-和Jπ=(1/2)+的各四个组态. 结果表明对于不同的模型, 不论 Jπ=(1/2)-和 Jπ=(1/2)+, T=0的态的能量总是最低的. 但是最低态的能量的理论计算值仍比Θ质量的实验值高250—300 MeV.     

手征夸克模型下udss四夸克态的研究

在手征SU(3)夸克模型和扩展的手征SU(3)夸克模型的框架下, 用变分的方法系统地研究了同位旋为0、1, 自旋宇称为0⁺、1⁺和2⁺的udss四夸克系统6个低组态的能量. 模型的参数取自以前的工作, 它能很好地描述核子-核子散射相移以及核子-超子散射截面. S道相互作用的参数由拟合K介子和K^*介子的质量定出, 并且考虑了具有相同量子数的态之间的态混合效应. 结果表明, 同位旋为0且自旋宇称为1⁺的udss能量低于相应的K^*K^*,的阈能, 且该组态中KK^*的成分相当小, 因此该组态的宽度可能较小, 可视为一个可能的四夸克态的候选者.     

夸克─夸克等效相互作用与手征对称性

从手征变换不变的要求出发给出了一个包括四种场交换的夸克－夸克等效相互作用势．用处理集团模型的共振群方法计算了核子－核子散射３Ｓ１和１Ｓ０态的相移．较好地解释了以往夸克势模型计算中１Ｓ０态相移与实验之间的差距．     

多夸克态研究概况

介绍了多夸克态研究的重要性,侧重介绍了最近发现的5夸克态的实验和理论研究现况.     

Fe1.01Se0.4Te0.6单晶的超导电性研究

本文采用自助溶剂法生长得到Fe1.01Se0.4Te0.6单晶样品,超导零电阻温度Tczero=11.0 K,部分样品经400℃进行48小时退火之后,超导零电阻温度变为Tczero=7.0K.分析表明退火后样品的Fe含量变大,超导电性被部分抑制.通过磁场下电阻率-温度曲线的实验测量,用WHH(Werthamer-Helfand-Hohenberg)方法估算得到退火前后样品在0K附近的上临界场分别为83.2T和61.3T.上临界场μ0Hc2(T)随温度变化曲线在0T附近向高温方向上翘,说明样品具有"二流体"行为.直流磁化曲线在40K和120K分别出现向下弯曲,40K处的变化可能对应于过量Fe的自旋冻结.应变测量结果显示样品在117K时应变值发生一个突变,变化量约为晶格参数的0.06%,显示样品发生一个结构相变.因此,120K处的磁化下降对应于样品从四方相到正交相的结构转变.     

The nu(12) Band of CH(3)SiD(3)

The lowest frequency degenerate fundamental band of CH(3)SiD(3) (v(12) = 1 <-- 0) centered around 418 cm(-1) was measured in order to investigate the vibration-torsion-rotation interactions in a symmetric-top molecule with a single torsional degree of freedom. The spectrum was recorded at an instrumental resolution of 0.004 cm(-1) using a Bomem Fourier transform spectrometer. The temperature and pressure of the sample were 180 K and 2 Torr, respectively. Because of the Coriolis coupling between the torsional stack with one quantum of the silyl rock excited and the corresponding stack for the ground vibrational state, torsional splittings are measured that are substantially larger than expected simply from the observed increase in the barrier height. Due to the local nature of the Coriolis perturbation, the significantly enhanced torsional splittings are confined to a few (K, varsigma) rotational series; here varsigma = -1, 0, 1 labels the torsional sublevels. The current measurements of the nu(12) band and frequencies from previously reported studies in the ground vibrational state were fitted to within experimental uncertainty using an effective Hamiltonian which was used for the analyses of similar spectra in CH(3)SiD(3) and CH(3)CD(3). Spectroscopic parameters characterizing the states v(12) = 0 and 1 and their interactions were determined, including several Coriolis-coupling constants. Copyright 2000 Academic Press.     

N(2)-Broadening Coefficients in the nu(1) Band of (35)Cl(12)C(14)N

N(2)-broadening coefficients have been measured for 30 lines of cyanogen chloride ((35)Cl(12)C(14)N) at room temperature in the P and R branches of the nu(1) band, using a tunable diode-laser spectrometer. These lines, with J values ranging from 0 to 55, are located in the spectral range 694-736 cm(-1). The collisional widths are obtained by fitting the spectral lines with a Voigt and a Rautian profile. The broadenings coefficients of (35)ClCN-N(2) have also been calculated from a semiclassical theory involving the atom-atom Lennard-Jones model for the intermolecular potential in addition to electrostatic interaction. Copyright 2000 Academic Press.     

CO2同位素分子16O12C16O, 16O12C17O, 16O13C17O配分函数研究

本文主要研究了CO2的三种同位素分子16O12C16O , 16O12C17O ,16O13C17O 70 K~6000 K的总内配分函数 (TIPS)。在总内配分函数的计算中, 转动配分函数的计算采用了McDowell的解析式法, 振动配分函数则采用了简谐振动近似(HOA)获得。最后通过将两配分函数乘积近似计算得出TIPS, 并将其70~3000 K的数据和HITRAN04数据进行了比较, 发现所得结果和数据库符合的较好, 且其误差可以近似看成一条直线。并通过对误差的拟合修订了高温区(3000~6000 K)的计算数据, 给出了在高温下的较为准确的TIPS值。     

Magnetic properties of (Co Pd ) superstructures on Pd(100) and Pd(111)

The magnetic properties of (Co_nPd_m)_r superstructures on Pd(100) and Pd(111) are evaluated using the fully-relativistic spin-polarized screened Korringa-Kohn-Rostoker method. It is found that only in the case of a Pd(111) substrate such superstructures exhibit perpendicular magnetism, while on a Pd(100) substrate the magnetization is oriented in-plane. Also investigated is the effect of interdiffusion in repeated superstructures. By using the inhomogeneous coherent potential approximation (CPA) for layered systems the effect of ordering into (repeated) superstructures can be described in an ab-initio-like manner. It is found that already small amounts of interdiffusion can be decisive for the actual value of the magnetic anisotropy energy. Received 3 November 1999 and Received in final form 18 January 2000     

Current-confined-path (CCP) giant magnetoresistive (GMR) sensors

Current-perpendicular-to the plane (CPP) giant magnetoresistive (GMR) sensors with a current-confined-path (CCP) layer inserted within the Cu spacer have been manufactured using ultrahigh vacuum PVD sputtering, photolithography, and ion milling processes. Compared with a pure metallic CPP system, the CCP insertion layer enables a substantial increase in sensor resistance with an equivalent or better GMR ratio, and thus a significant improvement in the ΔRA amplitude. Heads with such a sensor have been tested under various bias currents, both quasistatically and on a spinstand. It was found that the resistance of the sensors increases with increasing bias current and voltage, following typical metallic behavior. Also, the CCP insertion layer enables operation at higher bias currents compared with the pure metallic sensors (without the insertion layer) and thus a higher output signal. This effect is attributed to less magnetic instability due to the reduced Ampere fields around the narrow (∼6 nm) current-confined paths. Finally, the CPP-GMR heads with CCP layer were tested under high-density recording conditions using the perpendicular recording media. Bit error rate (BER) as a function of linear density is reported. Microtrack profiles were also recorded to determine track density capability.     

Simultaneous Analysis of the nu(2) Raman and nu(2) + nu(6) Infrared Spectra of the SF(6) Molecule

High-resolution Raman spectra of the nu(2) band of SF(6) have been recorded at a temperature of 195 K (dry ice) and a pressure of 39 mbar. These spectra were analyzed using a new set of programs specially written for XY(6) molecules. These programs, called HTDS (highly spherical top data system) in reference to the set of programs called STDS (spherical top data system written for XY(4) molecules) can be freely accessible through ftp (user anonymous) at jupiter.u-bourgogne.fr or on the web at the URL http://www.u-bourgogne.fr/LPUB/shTDS.html. The study of nu(2) was made using a Hamiltonian developed through the third order. Four parameters were determined. The standard deviation obtained using about 559 data up to J < 61 is 0.0021 cm(-1). This result is used to refine by simultaneous analysis the nu(2) and nu(2) + nu(6) bands of SF(6). This new fit allows the determination for the first time of some nu(6) parameters. The values obtained for this band (forbidden in Raman and in infrared) will be used to study the infrared hot bands in the nu(3) and nu(4) regions. Copyright 2000 Academic Press.     

First Observation of the nu(17)-nu(4) Difference Bands of Diborane (10)B(2)H(6) and (11)B(2)H(6)

An analysis of the nu(17)-nu(4) difference bands near 800 cm(-1) of two isotopic species, (10)B(2)H(6) and (11)B(2)H(6), of diborane has been carried out using infrared spectra recorded with a resolution of ca. 0.003 cm(-1). In addition, the nu(17) band of (10)B(2)H(6) has been recorded and assigned. Since this band in (11)B(2)H(6) had already been studied (R. L. Sams, T. A. Blake, S. W. Sharpe, J.-M. Flaud, and W. J. Lafferty, J. Mol. Spectrosc. 191, 331-342 (1998)), it was possible to derive precise energy levels and Hamiltonian constants for the 4(1) vibrational states of both isotopic species. Copyright 2000 Academic Press.     

High-Resolution FTIR Spectrum of the nu(9) Band of Ethylene-D(4) (C(2)D(4))

The spectrum of the nu(9) fundamental band of ethylene-d(4) (C(2)D(4)) has been measured with an unapodized resolution of 0.004 cm(-1) in the frequency range of 2300-2400 cm(-1) using a Fourier transform infrared spectrometer. A total of 549 transitions have been assigned and fitted using a Watson's A-reduced Hamiltonian in the I(r) representation to derive rovibrational constants for the upper state (v(9) = 1) up to five quartic terms with a standard deviation of 0.00087 cm(-1). They represent the most accurate rovibrational constants for the nu(9) band so far. About 30 transitions of K(a)(') = 0, one transition of nu(9) which were identified to be perturbed possibly by the nearby nu(11) and nu(2) + nu(12) transitions, were not included in the final fit. The nu(9) band of C(2)D(4) was found to be basically B-type with an unperturbed band center at 2341.836 94 +/- 0.000 13 cm(-1). Copyright 2000 Academic Press.     

Theoretical Study of the Collision-Induced Double Transition CO(2) (nu(3) = 1) + N(2) (nu(1) = 1) <-- CO(2) (nu(3) = 0) + N(2) (nu(1) = 0) at 296 K

A procedure is presented for the calculation of the double vibrational collision-induced absorption CO(2) (nu(3) = 1) + N(2) (nu(1) = 1) <-- CO(2) (nu(3) = 0) + N(2) (nu(1) = 0) on the basis of quantum lineshapes computed using an isotropic potential and dipole-induced dipole functions. The linestrengths and energies of the vibration-rotation transitions are treated explicitly for N(2), utilizing the HITRAN database for CO(2). The theoretical absorption profile is compared to recent experimental results. By narrowing the width of the individual lines contributing to the overall absorption profile relative to their values determined for N(2)-N(2) collision-induced absorption, excellent agreement between theory and experiment is obtained. Copyright 2000 Academic Press.