用玻色子组态混合和玻色子表面δ相互作用研究核谱

用玻色子组态混合波函数和玻色子表面δ相互作用研究了三玻色子核⁴⁶Ti和⁵⁴Cr的sdgIBMI的能谱和E2跃迁概率,理论计算结果令人满意,比sdIBMI能拟合出更多的能级和E2跃迁概率,而且它们的误差更小. 说明g玻色子在振动区也起着重要的作用,同时进一步证明了这种玻色子组态混合模型是成功的.     

Numerical simulation of soft palate movement and airflow in human upper airway by fluid-structure interaction method

In this paper, the authors present airflow field characteristics of human upper airway and soft palate movement attitude during breathing. On the basis of the data taken from the spiral computerized tomography images of a healthy person and a patient with Obstructive Sleep Apnea-Hypopnea Syndrome (OSAHS), three-dimensional models of upper airway cavity and soft palate are reconstructed by the method of surface rendering. Numerical simulation is performed for airflow in the upper airway and displacement of soft palate by fluid-structure interaction analysis. The reconstructed three-dimensional models precisely preserve the original configuration of upper airways and soft palate. The results of the pressure and velocity distributions in the airflow field are quantitatively determined, and the displacement of soft palate is presented. Pressure gradients of airway are lower for the healthy person and the airflow distribution is quite uniform in the case of free breathing. However, the OSAHS patient remarkably escalates both the pressure and velocity in the upper airway, and causes higher displacement of the soft palate. The present study is useful in revealing pathogenesis and quantitative mutual relationship between configuration and function of the upper airway as well as in diagnosing diseases related to anatomical structure and function of the upper airway. The project supported by the National Natural Science Foundation of China (10672036, 10472025 and 10421002), the Natural Science Foundation of Liaoning Province (20032109). English text was polished by Yunming Chen.     

Pressure-Induced Shifts of R1 and R2 Lines of YAG:Cr3+

By means of improved ligand-field theory, the "pure electronic" pressure-induced shifts (PS's) and the PS's due to electron-phonon interaction (EPI) of R1 line and R2 line of YAG:Cr3 have been calculated, respectively.The calculated results are in very good agreement with the experimental data. It is demonstrated that the admixture of |t22(3T1)e4T2> and |t322E> bases in the wavefunction of R1 level of YAG:Cr3 and its change with pressure play a key role for the PS of R1 line. The behaviors of the "pure electronic" PS of R1 line and the PS of R1 line due to EPI are different. It is the combined effect of them that gives rise to the total PS of R1 line, which has satisfactorily explained the experimental results. The systematic analyses and comparisons between the feature of R1-line PS of YAG:Cr3 and the ones of three laser crystals (GSGG:Cr3 , GGG:Cr3 and ruby) have been made, and the origin of the difference between them has been revealed.     

Bending-torsion vibration of a partially submerged cylinder with an arbitrary cross-section

An analytical method is presented to investigate the bending-torsion vibration characteristics of a cylinder with an arbitrary cross-section and partially submerged in water. The compressibility and the free surface waves of the water are considered simultaneously in the analysis. The exact solution of structure–water interaction is obtained mathematically. Firstly, the analytical expression of the velocity potential of the water is derived by using the method of separation of variables. The unknown coefficients in the velocity potential are determined by the longitudinal and circumferential Fourier expansions along the outer surface of the cylinder and are expressed in the form of integral equations including the unknown dynamic bending deflection and torsional angle of the cylinder. Secondly, the force and torque acting on the cylinder per unit length, provided by the water, are obtained by integrating the water dynamic pressure along the circumference of the cylinder. The general solution of bending-torsion vibration of the cylinder under the water dynamic pressure is derived analytically. The integral equations included in the velocity potential of the water can be solved exactly. Finally, the eigenfrequency equation of cylinder–water interaction is obtained by means of the boundary conditions of the cylinder. Some numerical examples for elliptical columns partially submerged in water are provided to show the application of the present method.     

70 GHz二次谐波倍频回旋速调管研究

 对70 GHz二次谐波倍频回旋速调管高频结构和电子与波互作用进行了研究。研究了TE02模腔体绕射品质因数及模式转化，解决了二次谐波倍频回旋速调管漂移段不能截止70 GHz的TE01模而引起的腔体间高频串扰的问题。分析了注电流、输入功率、电子横纵速度比和电子注引导中心半径等参数对输出功率、增益和效率的影响。针对二次谐波回旋速调管放大器工作频带窄、效率低，进行了高频结构优化设计，显著地展宽了工作频带，提高了互作用效率。在理论分析和高频计算的基础上，建立了注-波互作用PIC（粒子模拟）模型，进行了粒子模拟计算和优化，得到了70 GHz 的二次谐波倍频四腔回旋速调管放大器设计方案。粒子模拟结果表明：在工作电压70 kV，注电流13 A，电子注横向速度与纵向速度比为1.5时，中心频率69.81 GHz输出功率256 kW，带宽160 MHz，电子效率28%，饱和增益大于44 dB。     

相互作用对玻色气体热力学性质及稳定性的影响

根据由赝势法得到的非理想玻色气体的自由能和状态方程，研究了相互作用对凝聚温度的影响.从热力学角度揭示了存在引力作用时定压热容量、等温压缩系数、定压膨胀系数的反常热力学特性.研究了引力作用下玻色气体系统的不稳定性，给出了不稳定性的温度判据和粒子数密度判据. 关键词： 相互作用 玻色气体 热力学性质 不稳定性判据     

外加磁场微波等离子推力器内流场数值模拟

为了提高微波等离子推力器性能，改善等离子体对电磁波能量的吸收状况，提高核心区温度，提出外加磁场的方案，并对热等离子体进行了数值模拟.假设局域热平衡条件，采用Navier-Stokes，Maxwell和Saha方程，利用压力修正的半隐格式和时域有限差分求解方法，建立了径向磁镜场下推力器内等离子体流场的数值计算模型.数值模拟结果表明：外加磁场后的磁感应强度小于0.5 T时，推力器内热等离子体核心区最高温度随磁感应强度的增加而迅速提高.外加磁场后的磁感应强度大于0.5 T时，核心区最高温度随磁感应强度的增加而缓慢提高.磁感应强度为0.5 T时，热等离子体核心区最高温度与不加磁场相比提高了24%.外加磁场对等离子体流场速度分布影响不大. 关键词： 等离子体模拟 等离子体相互作用 等离子体流动     

Interaction of metals with an organic semiconductor: Ag and In on PTCDA

The interaction of Ag and In with a thin film of 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA) was studied by near-edge X-ray absorption fine structure (NEXAFS). Upon Ag deposition on a PTCDA film of 20 nm thickness the relative intensities and lineshapes, as well as the angular dependence of the spectra remains unchanged, illustrating the formation of a chemically unreactive Ag/PTCDA interface. On the other hand, the adsorption of 0.3 nm In strongly decreases the intensity of the π^* resonances in C and O K-edge NEXAFS spectra. This is attributed to a strong charge transfer between In and PTCDA, leading to a redistribution of the charge in the molecule. However, the absence of a strong shift or new features and negligible dependence of peak intensities corresponding to π^* resonances on the In thickness indicate that the interaction between In and PTCDA is not accompanied by a covalent bond formation.     

利用手征SU(3)夸克模型研究轻双Λ超核^6_ΛΛHe,^5_ΛΛHe,^5_ΛΛH,^4_ΛΛHe,和^4_ΛΛH的结合能

在手征SU(3)夸克集团模型下, 通过共振群方法(RGM)计算了双Λ超核^6_ΛΛHe,^5_ΛΛHe,^5_ΛΛH,^4_ΛΛHe,和^4_ΛΛH的结合能. 结果表明, 假定双Λ超核具有双Λ集团和壳心核集团构成的两集团结构, 得到的^6_ΛΛHe超核的结合能与实验值基本吻合, 表明手征SU(3)夸克集团模型不仅能较好地描述重子谱、N-N和Y-N相互作用及轻Λ超核的结合能, 也能较好地描述Y-Y相互作用及双Λ超核^6_ΛΛHe,^5_ΛΛHe,^5_ΛΛH,^4_ΛΛHe,和^4_ΛΛH的结合能, 指出了它们存在的可能性.     

Bipyridinophane‐containing conjugated polymers modulated with an intramolecular aromatic C?H/π interaction

Bipyridinophane–fluorene conjugated copolymers have been synthesized via Suzuki and Heck coupling reactions from 5,8‐dibromo‐2,11‐dithia[3]paracyclo[3](4,4′)‐2,2′‐bipyridinophane and suitable fluorene precursors. Poly[2,7‐(9,9‐dihexylfluorene)‐co‐alt‐5,8‐(2,11‐dithia[3]paracyclo[3](4,4′)‐2,2′‐bipyridinophane)] ( P7 ) exhibits large absorption and emission redshifts of 20 and 34 nm, respectively, with respect to its planar reference polymer Poly[2,7‐(9,9‐dihexylfluorene)‐co‐alt‐1,4‐(2,5‐dimethylbenzene)] ( P11 ), which bears the same polymer backbone as P7 . These spectral shifts originate from intramolecular aromatic C? H/π interactions, which are evidenced by ultraviolet–visible and ¹H NMR spectra as well as X‐ray single‐crystal structural analysis. However, the effect of the intramolecular aromatic C? H/π interactions on the spectral shift in poly[9,9‐dihexylfluorene‐2,7‐yleneethynylene‐co‐alt‐5,8‐(2,11‐dithia[3]paracyclo[3](4,4′)‐2,2′‐bipyridinophane)] ( P10 ) is much weaker. Most interestingly, the quenching behaviors of these two conjugated polymers are largely dependent on the polymer backbone. For example, the fluorescence of P7 is efficiently quenched by Cu²⁺, Co²⁺, Ni²⁺, Zn²⁺, Mn²⁺, and Ag⁺ ions. In contrast, only Cu²⁺, Co²⁺, and Ni²⁺ ions can partially quench the fluorescence of P10 , but much less efficiently than the fluorescence of P7 . The static Stern–Volmer quenching constants of Cu²⁺, Co²⁺, and Ni²⁺ ions toward P7 are of the order of 10⁶ M^?1, being 1300, 2500, and 37,300 times larger than those of P10 , respectively. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4154–4164, 2006