Ar原子偶宇称3p5(2P1/2)nl′ [K′]J (l′=1, 3)自电离Rydberg态共振增强激发光谱

用脉冲直流放电产生Ar原子亚稳态3p⁵4s[3/2]₂和3p⁵4s′[1/2]₀．在单光子32500～35600 cm^-1能量范围内, 结合飞行时间质谱技术获得Ar原子共振增强激发光谱．光谱分析表明,所有谱线来源于Ar原子3p⁵4s[3/2]₂和3p⁵4s′[1/2]₀两个亚稳态吸收单个光子向偶宇称np′、nf′自电离Rydberg态序列的跃迁．实验观测到许多新的自电离能级,并获得更精确和系统的能级位置和量子亏损值数据．     

超高泵浦功率下的Xe(6p[1/2]0, 6p[3/2]2, 和6p[5/2]2)原子的能量转移过程

本文研究了Xe(6p[1/2]₀, 6p[3/2]₂, and 6p[5/2]₂)原子在聚焦条件下的动力学过程. 激发能级的原子密度在聚焦条件下会显著地增加,因此两个高激发态原子之间的energy-pooling碰撞的概率也会增加. 这种energy-pooling碰撞主要有三种类型. 第一种类型为energy-pooling碰撞导致的电离. 一旦将激发激光聚焦,就可以从侧面的窗口观察到非常明显的电离现象,不论激发能级是6p[1/2]₀、6p[3/2]₂或6p[5/2]₂能级. 这种电离的产生机理是energy-pooling电离或者一个Xe^*原子再吸收一个光子产生电离. 第二种类型为跨越较大能极差的energy-pooling碰撞. 当激发能级为6p[1/2]₀能级的情况下,两个6p[1/2]₀原子碰撞会产生一个5d[3/2]₁原子和一个6s''[1/2]₀原子. 第三种类型为跨越较小能级差的energy-pooling碰撞. 以5个二次产生的6p能级为上能级的荧光强度都变得更强,并且这些荧光的上升沿都变得更陡峭. 产生这些6p原子的主要机理是energy-pooling碰撞并非简单的碰撞弛豫. 基于理想气体原子之间的碰撞概率公式,推导出两个6p[1/2]₀原子的energy-pooling碰撞速率为6.39x10⁸s^-1. 此外,6s原子在聚焦条件下的密度也会增加. 因此所有的荧光曲线会因为辐射俘获效应而出现非常严重的拖尾.     

Ar原子偶宇称3p5(2P1/2)nl''[K'']J(l''=1,3)自电离态激发谱线形研究

The even-parity autoionizing resonance series 3p⁵np''[3/2]_1,2, 3p⁵np''[1/2]₁, and 3p⁵nf''[5/2]₃ of Ar have been investigated exciting from the two metastable states 3p⁵4s[3/2]₂ and 3p⁵4s''[1/2]₀ in the photon energy range of 32500-35600 cm^-1 with an experimental bandwidth of ~0.1 cm^-1. The excitation spectra of the even-parity autoionizing resonance series show typical asymmetric line shapes. New level energies, quantum defects, line profile index and resonance widths, resonance lifetime and reduced widths of the autoionizing resonances are derived by a Fano-type line-shape analysis. The line profile index q and the resonance widths Γ are shown to be approximately proportional to the effective principal quantum number n^*. The line separation of the 3p⁵np'' autoionizing resonances is discussed.     

碱金属Li,Na,K,Rb,Cs,Fr的ns2S1/2,np2P1/2,3/2, nd2D3/2,5/2 和nf2F5/2,7/2 里德伯能级理论研究

本文在多通道量子数亏损理论(MQDT)框架下,利用相对论多通道理论(RMCT),分别在冻结实近似、 考虑Δl=-1的偶极极化效应、Δl=+1的偶极极化效应、Δl=± 1的偶极极化效应、伸缩模效应以及同时考虑偶极极化效应和伸缩模效应等不同层次近似下,系统地计算了碱金属Li, Na, K, Rb, Cs和Fr七个里德伯系列的能级,即ns²S_1/2, np²P_1/2, np²P_3/2, nd²D_3/2, nd²D_5/2, nf²F_5/2 和nf²F_7/2.计算结果表明,电子关联效应对碱金属原子的里德伯能级的影响很大.总的来说,偶极极化效应比伸缩模效应重要,而在偶极极化效应中, Δl = + 1的偶极极化效应比Δl = - 1的偶极极化效应重要.但对于Na的ns²S_1/2,(nd²D_3/2,nd²D_5/2)里德伯系列的能级,和Li的(np²P_1/2,np²P_3/2)里德伯系列的能级,是伸缩模效应比较重要.     

F2 Σ+ -X 2Σ +Band System of Cobalt Carbide

用脉冲直流放电产生Xe原子亚稳态5p56s[3/2]2和5p56s′[1/2]0.在单光子28000－42000cm-1能量范围内,结合飞行时间质谱技术获得Xe原子共振增强激发光谱.光谱分析表明,所有谱线来源于Xe原子5p56s[3/2]2和5p56s′[1/2]0两个亚稳态吸收单个光子向偶宇称np′、nf′自电离Rydberg态序列的跃迁.实验观测到许多新的自电离能级,并获得更精确和系统的能级位置和量子亏损值数据.     

Yb3+:Gd2SiO5晶体的结构和光谱性能

采用提拉法成功生长尺寸为φ30 mm× 75 mm的15at.%Yb³⁺:Gd₂SiO₅单晶, 并用Reitveld全谱拟合方法确定了其晶格常数、原子坐标和温度因子等参数. 用吸收光谱计算了Yb³⁺离子²F_7/2↔ ²F_5/2能级跃迁的振子强度、谱线强度、跃迁概率、 能级寿命和积分发射截面等光谱参数, 并根据激光性能评估得出结论: 表明该晶体具有较大的阈值特性, 有望采用大功率激光二极管泵浦实现可调谐或超快激光输出.     

π-Λ耦合常数和π-Λ低能P3/2波散射

本文将改进的Chew-Low展开应用到π-A的P_3/2分波散射,以从共振参量(能级和宽度)来确定π∧∑的耦合常数和P_3/2相移随能量的变化。当共振宽度采用目前比较公认的值50MeV时,给出的π-A耦合常数为g²=34或f²=0.12.文中亦给出了其他可能的宽度值所相应的结果。所得到的P_3/2相移曲线虽无实验可以比较,但估计在质心系总能量W≈1450MeV以下,应该是可靠的。     

Cs2 23△1g态碰撞线归属和超精细结构解释

根据最新的Cs₂分子中间态A¹∑⁺_u -b³Πu全局解微扰获得的能级数据, 归属了通过微扰增强红外-红外光学双共振中间态A¹∑⁺_u 到上态2³△_1g的140条碰撞线, 包含之前实验观测到的221条2³△_1g←A¹∑⁺_u← X¹∑⁺_g 双共振跃迁[J. Chem. Phys. 128, 204313 (2008)], 重新计算了2³△_1g态的分子常数和势能曲线(排除54个微扰能级). 本次拟合得到的离心畸变常数和从经验公式计算得到的值相符合. 在亚多普勒激发光谱中,没有分辨出2³△_1g态的超精细结构. 对2³△_1g态的超精细结构进行初步计算,比较实验结果给出解释和说明.     

179Au的1/2[660](πi13/2)转动带

利用能量为164—180MeV的³⁵Cl束流,通过重离子核反应¹⁴⁹Sm(³⁵Cl,5n)研究了¹⁷⁹Au的高自旋态能级结构.实验进行了γ射线的激发函数、X-γ和γ-γ-t符合测量.基于对实验测量结果的分析,首次建立了¹⁷⁹Au的1/2[660](πi_13/2)转动带.结合已有的实验数据,着重讨论了奇AAu核中1/2[660](πi_13/2)转动带的带头激发能随中子数的变化     

CO2对790 nm附近水线的压力加宽和位移

采用高灵敏的激光光腔衰荡光谱技术研究了CO₂对¹⁶O水分子v²+3v³振动带跃迁线的压力诱导效应. 为了抑制水的自碰撞效应,水的压力在实验中低于0.5 Torr. 基于铷原子吸收线和超稳法布里-珀罗标准确定了跃迁谱线高达10^-5 cm^-1精度的绝对频率. 采用软碰撞模型对吸收线进行模拟,获得了对应的线形参数.     

Linear-chain antiferromagnetism in Ni(N2H5)2(SO4)2

The compound dihydrazinium bis(sulfato) niccolate(II), Ni(N₂H₅)₂(SO₄)₂, containing sulfato-bridged chains of Ni(II) ions, can be described as an antiferromagnetic Heisenberg linear-chain system. A reasonable agreement of susceptibility measurements in the temperature region 2–80K, with a theory developed by Weng for antiferromagnetic Heisenberg linear chains with spin S=1, is obtained for a value of the intra-chain interaction $\text{J}\text{k}\text{=?3.35K}$. Preliminary results of specific heat measurements, on the other hand, do not fit quite well using this model. The origin of this discrepancy is suggested to be a zero-field splitting of the single ion.     

Phonon coupled cooperative low-spin 1A1high-spin 5T2 transition in [Fe(phen)2(NCS)2] and [Fe(phen)2(NCSe)2] crystals

Heat capacities of [Fe(phen)₂(NCS)₂] and [Fe(phen)₂(NCSe)₂] were measured between 13⁵ and 375 K. A heat capacity anomaly due to the spin-transition from low-spin ¹A₁ to high-spin π₂ electronic ground state was found at 176·29 K for the SCN-compound and at 231·26 K for the SeCN-compound, respectively. Enthalpy and entropy of transition were determined to be ΔH = 8·60 ± 0·14 kJ mol^?1 and ΔS = 48·78 ± 0·71 J K^?1 mol^?1 for the SCN-compound and ΔH = 11·60 ± 0·44 kJ mol^?1 and ΔS = 51·22 ± 2·33 J K^?1 mol^?1 for the SeCN-compound. To account for much larger value of ΔS compared with the magnetic contribution, we suggest that there is significant coupling between electronic state and phonon system. We also present a phenomenological theory based on heterophase fluctuation. Gross aspects of magnetic, spectroscopic, and thermal behaviors were satisfactorily accounted for by this model. To examine closely the transition process, infrared spectra were recorded as a function of temperature in the range 4000 ? 30 cm^?1. The spectra revealed clearly the coexistence of the ¹A₁, and the ⁵T₂ ground states around T_c.     

Magnetic susceptibility studies of (CH2)3(NH3)2FeCl2Br2 and (CH2)6(NH3)2FeCl2Br2

The magnetic susceptibility of the layered compounds (CH₂)₃(NH₃)₂FeCl₂Br₂ and (CH₂)₆(NH₃)₂FeCl₂Br₂ has been measured in the range 80 < T < 300 K. The results follow a Curie-Weiss behavior in the range 120 < T < 300 K but are field dependent for T < 120 K. The results are interpreted in terms of a two-dimensional antiferromagnetic interaction which is canted. A comparison with the corresponding pure chloride compounds is given.     

Electromechanical and ferroelectric properties of (Bi1/2Na1/2)TiO3-(Bi1/2K1/2)TiO3- (Bi1/2Li1/2)TiO3-BaTiO3 lead-free piezoelectric ceramics for accelerometer application

Lead-free (0.90-x)(Bi_1/2Na_1/2)TiO₃-0.05(Bi_1/2K_1/2)TiO₃-x(Bi_1/2Li_1/2)TiO₃-0.05BaTiO₃ piezoelectric ceramics (abbreviated as BNKLBT-100x, with x ranged from 0 to 2.5 mol %) were prepared by a conventional mixed oxide method. Effects of the amount of (Bi_1/2Li_1/2)TiO₃ (BLT) on the electrical properties and crystal structure of the BNKLBT ceramics were examined. BNKLBT-1.5 ceramics have good properties with piezoelectric constant d₃₃=163 pC/N, electromechanical coupling factor k_p=0.33, k_t=0.53, relative permittivity ε_r=785 and dissipation factor cosδ=2.2% at 1 kHz. The sample has larger remnant polarization than BNKLBT-0 ceramics and the same coercive field as BNKLBT-0 ceramics. X-ray diffraction analysis shows that the incorporated BLT diffuses into the BNT–BKT–BT lattice to form a solid solution during sintering, but changes the crystal structure from rhombohedral to tetragonal symmetry at higher BLT amounts. Depolarization temperature (T_d) of the BNKLBT-100x ceramics increases from 102 °C to ∼136 °C for BNKLBT-0 to BNKLBT-2.5. BNKLBT-1.5 is used as the transduction element in compressive type accelerometer and its sensitivity is calibrated by the back-to back method. Within the ±2.5% tolerance, the lead-free accelerometer has a mean value of 2.97 pC/ms^-2 within 50 Hz–12.45 kHz and the lead-based accelerometer has a mean value of 4.34 pC/ms^-2 within 50 Hz to 8.24 kHz. PACS 77.22.Ej; 77.84.-s; 85.50.-n     

Decoupled magnetic subsystems in the random mixture FepCo1-p(C5H5NO)6(ClO4)2

Specific heat data on the random mixtures Fe_pCo_1-pL₆(ClO₄)₂, where L = C₅H₅NO, are presented. The Fe and Co magnetic atoms have competing anisotropies since the pure Fe and Co compounds are known to be good examples of the simple cubic, $\text{S =}\text{1}\text{2}$, Ising and XY magnet, respectively. The experimental data show the two magnetic subsystems in the mixtures to be almost completely decoupled, which is a consequence of the fact that the crystal field anisotropies of the Fe²⁺ and Co²⁺ ions, yielding g_∥ ? g_⊥ and g_⊥ ? g_∥, respectively, are very strong compared to the magnetic exchange interactions. Consequently the two magnetic subsystems experience one another as nonmagnetic impurities. A model is presented which explains these results, as well as those previously found for related random mixtures, in terms of two interpenetrating percolation clusters.     

Electronic spectra and nature of transitions in [NH2(C2H5)2]2CuxZn1?xCl4 (x = 0.5, 1) crystals

The absorption spectra of the [NH₂(C₂H₅)₂]₂CuCl₄ crystals grown from a solution in ethyl alcohol and also of solid solutions of [NH₂(C₂H₅)₂]₂Zn_0.5Cu_0.5Cl₄ in the visible spectral region have been investigated in the vicinity of thermochromic phase transitions. It is shown that the phenomenon of thermochromism in these crystalline compounds is primarily related to the replacement of the square-planar geometry of the coordination surrounding of the Cu²⁺ ion by a tetrahedral one.Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 71, No. 6, pp. 798–802, November–December, 2004.This revised version was published online in April 2005 with a corrected cover date.     

A comparative study of dielectric and Raman spectroscopy of Pb(Y b1/2Ta1/2)O3 and Pb(Y b1/2Nb1/2)O3

A comparative study of the properties of two highly ordered lead based complex perovskites Pb(Y b_1/2Ta_1/2)O₃ and Pb(Y b_1/2Nb_1/2)O₃ has been carried out through x-ray diffraction, dielectric and Raman scattering measurements. These two compounds differ significantly in their structure, dielectric response and phonon vibration although the ionic radii and valencies are same for Ta and Nb. The room temperature x-ray diffraction pattern and Raman spectra show that the symmetry of lead ytterbium tantalate is lower than that of lead ytterbium niobate. The Raman spectra of Pb(Y b_1/2Ta_1/2)O₃ also indicates the presence of local distortion in the lattice which may be one of the factors responsible for the existence of a secondary transition.     

Antiferromagnetic resonance of (C2H5NH3)2CuCl4

Antiferromagnetic resonance of (C₂H₅NH₃)₂CuCl₄ was studied at 1 GHz region. Characteristics of a weak exchange interaction with a strong anisotropy were observed.     

铁电磁体Pb(Fe1/2Nb1/2)O3的磁电性能研究

对铁电磁体Pb(Fe_1/2Nb_1/2)O₃单晶样品中的 介电和磁性能进行了研究. 认为在其反铁磁相变点观察到的介电常数和损耗的异常来自于自发极化序和自旋序的相互作用 引起的磁电耦合. 磁矩与温度的关系曲线在Nel点以下的低温段呈上升趋势，测得的磁滞 回线证明有弱铁磁性出现. 对铁电磁体磁电相互作用的Monte Carlo模拟得到与实验类似的 结果. 关键词： 铁电磁体 1/2Nb_1/2)O₃')" href="#">Pb(Fe_1/2Nb_1/2)O₃ 磁电耦合 Monte Carlo模拟     

Electron paramagnetic resonance of Mn IN (NH4)2Co2(SO4)3 and (NH4)2Ni2(SO4)3 single crystals

EPR studies are reported on single crystals of ammonium cobalt sulphate and ammonium nickel sulphate containing Mn²⁺ ions. In each case only one magnetic complex of Mn²⁺ ion is found. The resonance lines in the case of Mn²⁺ doped ammonium nickle sulphate are characterised by a strong angular dependence of line intensities. The resonance lines in both the cases are fitted to a spin-Hamiltonian corresponding to orthorhombic symmetry.