输入腔高频场的矩阵分析

 应用模匹配理论推导和建立了单级突变的矩阵方程，并分析给出了具有多级突变和渐变结构级联情况下波导腔体的处理方法。在理论推导的基础上，通过编制程序计算出多级突变结构波导腔体模匹配系数级联矩阵，并由矩阵参数得到所需的腔体谐振频率和Q值等物理特性参量。实际计算结果表明，由程序模拟输入腔计算得到的数据结果与腔体的冷测实验结果基本一致，为进一步的注波互作用研究和回旋速调管的设计工作提供了参考依据。     

高速转镜干涉成像光谱仪的光程差分析

针对一种新的高速转镜干涉成像光谱仪的工作原理,给出其光程差的计算方法及结果.通过设定相关参量,重新构建光程差方程,并给出光程差在不同参量情况下的计算结果图,比较不同参量的影响.给出的光程差方程,为高速转镜干涉成像光谱仪的设计及获得的光谱图复原提供参量依据.     

硅波导受激喇曼散射放大信号光的数值模拟

提出了用连续泵浦光在硅波导中的受激喇曼散射对信号光进行放大的方法.建立了信号光和泵浦光在硅波导中传输的耦合方程,得到了计算信号光增益的理论模型.利用数值模拟结果,对泵浦功率沿波导的分布,信号光在不同波导长度以及输入功率情况下的增益等进行了分析和讨论.结果表明,适当增加波导长度和泵浦光功率可以得到较高喇曼增益的结论.     

移相干涉测量中的抗振技术

移相干涉测量技术是一种众所周知的非接触式的高精密测量方法,具有广泛的应用范围。环境振动是移相干涉仪测量误差的主要来源之一,国际上一些从事干涉测量的工作人员提出了许多抗振的方法,大体上分为主动技术和被动技术。主动抗振技术主要是系统自身探测振动并通过反馈回路对振动进行补偿,被动抗振技术则是通过各种技术措施尽量减小干涉仪对环境振动和气流影响的敏感度。从这两方面对干涉仪的抗振技术研究的进展做简单介绍,并介绍了作者所在课题组在这两个方面所进行的研究工作。     

质子椭圆流与对称能的密度依赖性

基于同位旋和动量依赖的强子输运IBUU04模型, 研究了¹³²Sn+¹²⁴Sn碰撞系统中的质子椭圆流对对称能的敏感关系. 研究发现入射能量从每核子400MeV到800MeV时质子椭圆流在低横动量端对对称能的敏感性高于高横动量端, 同时发现随着入射能量的增大, 质子椭圆流对对称能的敏感性在降低. 在研究入射能量范围内, 当入射能量为每核子400MeV左右时质子椭圆流对对称能最为敏感.     

从晕中子核引起核反应中提取对称势

利用同位旋相关量子分子动力学理论研究了中子晕核引起核反应机制中重要的同位旋效应以提取对称势. 因为同位旋相关量子分子动力学理论中的相互作用和介质中核子-核子碰撞截面都灵敏地依赖于碰撞系统的密度分布, 本项研究工作基于中子晕核扩展的密度分布. 该密度分布包含了反应机制中同位旋效应和疏散内部结构的平均特征. 为了弄清楚晕核引起核反应机制的同位旋效应, 在完全相同的入射道条件下, 比较了由中子晕核炮弹引起的同位旋效应和由相等质量的稳定核炮弹引起同位旋效应. 结果发现中子晕核炮弹引起的发射中子-质子比和同位旋分馏比明显大于相等质量稳定弹核产生的结果. 因而可以通过理论结果与实验数据的系统比较提取对称势.     

Probing Balance Energy Using Momentum- and Isospin-Dependent Potential

Using the momentum- and isospin-dependent Boltmann-Uehling-Uhlenbeck （BUU） model, we investigate the transverse flow and balance energy in two isotopic colliding systems ^48Ca＋^58Fe and ^48Cr＋^58Ni by adopting different symmetry potentials. By comparing the results between the two colliding systems, we find that the difference between the balance energies of two isotopic systems can be considered as a sensitive probe to the density dependence of symmetry energy.     

Oxidation of a ZnS nanobelt into a ZnO nanotwin belt or double single-crystalline ZnO nanobelts

Single-crystalline wurtzite ZnS nanobelts are synthesized by the vapor phase transport (VPT) process. When oxidized, a single-crystalline ZnS nanobelt turns into a ZnO nanotwin belt containing two twinning parts with a sharp and clear edge, which is a (0001) twinning plane parallel to and running through the length direction. The two twinning parts in a ZnO nanotwin belt have the same crystalline direction, [0001], along their width, and the and crystalline directions along the length direction. On some ZnO nanobelts, nanovoids appear along the twinning planes and when those nanovoids connect with each other, one original ZnS nanobelt can divide into two single-crystalline ZnO nanobelts with quite clear edges.     

Laser spectroscopy of VS: hyperfine and rotational structure of the CΣ-XΣ transition

The (0,0) and (0,1) bands of the C⁴Σ⁻-X⁴Σ⁻ electronic transition of VS (near 809 and 846 nm, respectively) have been recorded at high resolution by laser-induced fluorescence, following the reaction of laser-ablated vanadium atoms with CS₂ under supersonic free-jet conditions. A least squares fit to the resolved hyperfine components of the rotational lines gives the rotational constants and bond lengths as C⁴Σ⁻: , ; X⁴Σ⁻: , . The electron spin parameters for the two states show that there are some similarities between the states of VS and those of VO, but the hyperfine parameters show that the compositions of the partly filled molecular orbitals are by no means the same. The ground state Fermi contact parameter of VS, b(X⁴Σ⁻), is only 58% of that of the ground state of VO, which implies that the σ orbital of the ground σδ² electron configuration has less than 50% vanadium 4s character. Similarly, the excited state Fermi contact parameter, b(C⁴Σ⁻), is very much smaller than that of VO. No local rotational perturbations have been found in the C⁴Σ⁻ state of VS, though an internal hyperfine perturbation between the F₂ and F₃ electron components at low N confuses the hyperfine structure and induces some forbidden (ΔJ=±2) rotational branches.     

A study on new phase transitions in Cs2CaCl4·2H2O single crystals by observation of Cs NMR

The ¹³³Cs 1/2→−1/2 spin-lattice relaxation rate, , and the spin-spin relaxation rate, , for a Cs₂CaCl₄·2H₂O single crystal have been measured in function of temperature. The dominant relaxation mechanism of this crystal over the whole temperature range investigated here proceeds via quadrupole interaction. The changes in the ¹³³Cs spin-lattice relaxation rate near 325 K (=T_c1) and 360 K (=T_c2) correspond to phase transitions in the crystal. The change in the spin-lattice relaxation rate at T_c1 is small because the crystal lattice does not change very much during this phase transition. The change in near T_c2 is due to the critical slowing down of the soft mode that typically occurs in structural phase transitions. The temperature dependence of the spin-lattice relaxation rate for this crystal has maximum values at about 240 K, which is attributable to the effect of molecular motion as described by Bloembergen-Purcell-Pound theory. The phase transition temperatures T_c1 and T_c2 obtained from the temperature dependence of the relaxation rate is also clear from data obtained using differential scanning calorimetry. Therefore, we know that previously unreported phase transitions occur at 325 and 360 K.