U(N) SP(N) O(3)的分支律

利用群的直乘分解公式,考虑U(N)群的[2a1b]表示按群链U(N)SP(N)O(3)的约化规则,给出了相应的比较简单的分支律递推公式.该公式在用计算机计算分支律时,不受秩和表示维数的限制.为求解这类问题的分支律提供了一种比较简单的算法.在简化同位旋1/2的单j费米子体系的母分系数计算中具有十分重要的意义.用同样的方法也可以求出群链U(N)O(N)O(3)的分支律.     

Exciton–phonon interaction in Al_(0.4)Ga_(0.6)N/Al_(0.53)Ga_(0.47)N multiple quantum wells

The exciton-phonon interaction in Al_(0.4)Ga_(0.6)N/Al_(0.53)Ga_(0.47)N multiple quantum wells(MQWs) is studied by deepultraviolet time-integrated and time-resolved photoluminescence(PL).Up to four longitudinal-optical(LO) phonon replicas of exciton recombination are observed,indicating the strong coupling of excitons with LO phonons in the MQWs.Moreover,the exciton-phonon coupling strength in the MQWs is quantified by the Huang-Rhys factor,and it keeps almost constant in a temperature range from 10 K to 120 K.This result can be explained in terms of effects of fluctuations in the well thickness in the MQWs and the temperature on the exciton-phonon interaction.     

Al(N3)3和P(N3)3结构与性质的理论研究

在B3LYP/6-311++G(3df)理论水平,对二元叠氮化合物Al(N3)3和P(N3)3进行密度泛函理论计算研究,获得其稳定分子的几何构型、电子结构、红外光谱以及稳定性。研究结果表明,P(N3)3分子中的磷原子拥有一对孤对电子,给予临近氮原子(Nα)上的孤对电子较大斥力,从而使其表现出三角锥形结构特征,而Al(N3)3表现为平面三角形结构特征。自然键轨道分析表明,Al–Nα和P–Nα键本质上均属于共价键。与叠氮自由基相比较而言,Al(N3)3和P(N3)3的每个叠氮基内部的总成键度显著增大,从而导致N3基的振动频率发生明显蓝移。前线分子轨道能级差和叠氮自由基键离解能的计算结果均表明Al(N3)3比P(N3)3更稳定。     

Verhältnis des differentiellen (e,N)- zum totalen (γ,N)-Wirkungsquerschnitt

The ratio of the differential cross section for the (e, N)-process to the total (γ,N) -cross section is derived with the use of the relativistic Coulomb Eigenfunctions for the continuous spectrum. For electric and magnetic dipole transitions the Born approximation, the Coulomb correction, the effect of screening and that of finite nuclear size are calculated. In this angular distribution there should be no interference of electron waves scattered by different multipoles, where the inelastically scattered electrons are detected. Numerical calculations have been done for nuclei withZ=6, 29, and 82 and scattering anglesθ=1Ω, 132Ω, 160Ω and 180Ω of the electron. The result of this theory is compared with the experiments of W.C.Barber et al.     

Al(N3)3和P(N3)3结构与性质的理论研究

在B3LYP/6-311++G(3df)理论水平,对二元叠氮化合物Al(N3)3和P(N3)3进行密度泛函理论计算研究,获得其稳定分子的几何构型、电子结构、红外光谱以及稳定性.研究结果表明,P(N3)3分子中的磷原子拥有一对孤对电子,给予临近氮原子(Nα)上的孤对电子较大斥力,从而使其表现出三角锥形结构特征,而Al(N3)3表现为平面三角形结构特征.自然键轨道分析表明,Al-Nα和P-Nα键本质上均属于共价键.与叠氮自由基相比较而言,Al(N3)3和P(N3)3的每个叠氮基内部的总成键度显著增大,从而导致N3基的振动频率发生明显蓝移.前线分子轨道能级差和叠氮自由基键离解能的计算结果均表明Al(N3)3比P(N3)3更稳定.     

同位素~(15)N光电光谱分析

氮在自然界中有两种稳定性同位素,~(14)N(99.635%)和~(15)N(0.365%)。由于同位素~(15)N具有非放射性的特点,已被广泛用作标记原子,进行农业、土壤、生物、医学等过程研究。在各种同位素~(15)N分析方法中,光谱法由于仪器简单,操作方便,灵敏度和准确度较高,已成为一种广泛应用的重要方法,并生产了专门分析仪器。     

On the electronic structure of N,N′-ethylenebis(acetylacetonatiminato)Co(II), Co(II)acacen

Single crystal E.P.R. and cobalt ENDOR measurements on N,N′-ethylenebis(acetylacetonatiminato)Co(II), Coacacen, diluted in Niacacen·1/2 H₂O are reported. Forbidden Δm _Co = 1,2 transitions in the E.P.R. spectra have been observed. The g-tensor (E.P.R.) and the cobalt hyperfine and quadrupole tensors (ENDOR) have been determined. The g- and cobalt hyperfine tensors are discussed. They support the |² A ₂,yz? groundstate proposed for four coordinated low-spin Schiff base complexes of cobalt(II). The measured quadrupole coupling is also compatible with a |² A ₂,yz? groundstate, if anisotropic contraction of the cobalt 3d orbitals is taken into consideration.     

~(14)N ~(58)Ni和~(14)N ~(64)Ni深部非弹性反应产物同位素分布的差异

实验测得~(14)N(93兆电子伏) ~(58)Ni、~(64)Ni深部非弹性反应产物同位素分布,发现这两者存在系统性的差异。     

SU(2,2¦N) · 〈N′〉 superunified theory

We establish a superspaceU for supergauge actions, a conformal supergroupSU(2,2¦N), and a conformal extendedSU(2,2¦N) supergravity theory. Using the Lagrangian Higgs evolution mechanism under the supergroupSU(2,2¦N) SU(N) acting on the superspaceU, we advance anSU(2,2¦N)SUN superunified theory of a superunited system, discuss the Lagrangian evolution of the superunified theory, and give the fiber bundle geometry of all the above mechanisms.     

~(15)O-~(15)N,~(17)F-~(17)O库仑移位能

从Paris势和电磁相互作用出发,应用格林函数方法微观地计算了~(15)O-~(15)N,~(17)F-~(17)O库仑移位能.G矩阵的电荷非对称性的贡献较重要,比通常唯象的核力电荷非对称成分的贡献大一倍左右.     

Determination of the ~(12)C(p, γ)~(13)N reaction rates fromthe ~(12)C(~7Li,~6He)~(13)N reaction

The angular distribution of the 12C(7Li,6He)13N reaction at E(7Li) = 44.0 MeV was measured at the HI-13 tandem accelerator of Beijing, China. The asymptotic normalization coefficient (ANC) of 13N → 12C + p was derived to be (1.64 ± 0.11) fm-1/2 through the distorted wave Born approximation (DWBA) analysis. The ANC was then used to deduce the astrophysical S (E) factors and reaction rates for the 12C(p,γ)13N direct capture reaction at energies of astrophysical relevance.     

O(N)>O(N-1)约化因子

利用不可约张量基的概念和不可约张量算符的性质,给出了所有Ｏ（Ｎ）Ｏ（Ｎ－１）约化因子（ｍ１Ｎｍ２Ｎ…ｍ［Ｎ／２］Ｎ）（１０…０）的代数表达式． The algebraic expressions for all O(N)  O(N-1) reduction factors for (m 1N m 2N … m N )  (1 0 … 0) are given by using the concept of irreducible tensor basis and the properties of irreducible tensor operator.     

Electric field-induced hole injection-enhanced photoluminescence in a N,N’-bis(3-methylphenyl)-N,N’-bis(phenyl)-benzidine-based emitter

Non-monotonic, asymmetrical electric field dependence of photoluminescence （PL） intensity is observed in a mono- layer sample of tris-（8-hydroxyquinoline） aluminum （A1Q） doped N,N＇-bis（3-methylphenyl）-N,N＇-bis（phenyl）-benzidine （TPD）. A possible model is proposed： the charge separation from the dissociated photoexcited excitons causes energy band bending in the organic films and improves the hole injection from the electrode, which brings about the extra fluorescence. This mechanism is further verified by a series of experiments using a series of samples, variously featuring symmetrical electrodes, block layers, and hosts with lower hole mobilities.     

PS~(-1) Optical Interconnection of 2N×2N Using N×N Holographic Lens Array

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The Polarized Infrared Spectrum of Single Crystals of N,N′ -Ethylenebis(acetylacetoneiminato)-copper(II) Hemihydrate

In a previous paper¹ the infrared spectra of some chelates of the type N,N′-ethylenebis(acetylacetoneiminato)-metal(II) were reported and the vibrational assignments were made on a correlative basis and with the aid of the results of a normal coordinate treatment. In order to provide further data for a more reliable assignment of the vibrational spectra of this class of metal chelates an investigation was carried out on the infrared pleochroism of the single crystals of N,N′-ethylenebis(acetylacetoneiminato)-copper(II) (CuBae.1/2H₂0 in the following).     

Structure of Ti N (N = 6–15) titanium cluster isomers

The atomic structures of various isomers of free Ti _N (N = 6–15) titanium clusters have been studied by molecular dynamics using the many-body interaction potential in the tight binding model. The following parameters of the cluster structure have been calculated: average bond length and energy, coordination number, and frequencies (probabilities) of their appearance. An increase in the cluster size N is accompanied by increased values of these parameters. It is established that the frequency of appearance of an isomer with a given N value increases with the bond energy. The most probable structures of clusters with N = 10–15 correspond to maximum values of the atomic structure parameters among all isomers of a given size.     

Surface phonon dispersion of Cu(100)c(2×2)N

The Cu(100) surface covered with atomic nitrogen has been studied with low energy electron diffraction (LEED), Auger electron spectroscopy (AES) and inelastic electron scattering (EELS). Atomic nitrogen, formed by thermal dissociation of NH₃ adsorbed at 100 K, forms a c(2×2) overlayer on the Cu(100) surface. The dispersion of adsorbate and substrate associated modes of the Cu(100) surface covered with a c(2×2) nitrogen overlayer has been measured along the two dimensional Brillouin zone in the - by inelastic electron scattering. The experimental data are compared to a lattice dynamical slab calculation. The Rayleigh-mode (S₄-phonon) is only slightly changed by the N-overlayer. An optimum fit for the perpendicular and parallel nitrogen modes (=320 cm^–1 and =740 cm^–1 at =0.1) is obtained when the nitrogen atom is placed 0.6 Å above the first copper layer.     

The twisted SU(N) group. On the C *-algebra C(S μ U(N))

It is proved that C(S U(N)) is a type I C ^*-algebra.