色散关系和纵向耦合腔(C~3)对半导体激光器的模谱行为的影响

本文从理论上探讨了色散关系的作用,引进α_e和F因数,修正了半导体激光器的光谱线宽公式,发现通过波导结构的设计不但可减小α_e因数,还可增大F因数来进一步抑制光谱线宽,用所提出的等效反射率法分析了纵向耦合腔(C~3)的选模和压缩线宽的机制,指出实现单纵模窄线宽的条件。     

OH分子基态（X2Π）的结构与势能函数

采用密度泛函理论的B3LYP方法和二次组态相互作用(QCISD(T))方法优化计算了OH分子基态(X²Π)的平衡结构、振动频率和离解能.根据原子分子反应静力学原理，导出了OH分子基态(X²Π)的合理离解极限，采用最小二乘法拟合Murrell-Sorbie函数得到了相应的势能函数和与该基态相对应的光谱常数(B_e，α_e，ω_e和ω_eχ_e)，计算结果与实验数据符合得相当好. 关键词： OH分子 2Π)')" href="#">基态(X²Π) 势能函数     

C_2^+ (X^4 Σ_g^-,1^4 Σ_u^+)离子体系解析势能函数、光谱常数和振动能级研究

采用多参考组态相互作用(MRCI)方法,结合aug-cc-pV6Z(AV6Z)基组,计算了C₂⁺(X⁴Σ_g^-,1⁴Σ_u⁺)的势能曲线,计算过程中考虑了Davidson修正和相对论效应,并将结果外推至完备基组(CBS)的极限.基于得到的单点能量,用最小二乘法方法进行了Murrell-Sorbie函数拟合,得到了势能函数解析式(APEF).基于APEF,计算了C₂⁺(X⁴Σ_g^-,1⁴Σ_u⁺)离子体系的离解能D_e,平衡核间距R_e,光谱常数ω_e,ω_eχ_e,B_e,α_e,结果与实验和其他理论计算值符合...     

HF分子电子基态和激发态的MRCI计算

应用舍Davidson修正的多参考组态相互作用（MRCI）方法,在aug-cc-pVTZ基组水平上对HF基态及最低的多个单重和三重电子激发态进行了势能扫描计算.结合群论原理及分子的离解极限,分析了电子态势能曲线的特征,得出激发态B¹S⁺对应的离解极限为H⁺+F^-（¹S）.基于势能曲线,数值求解核运动的径向Schrodinge方程,得到J=0时束缚电子态X¹S⁺,B¹S⁺,C¹P和D¹S⁺的振动能级和转动常数,继而进行数据拟合得到电子态的光谱常数,基态X¹S⁺:ω_e=4146.94 cm^-1,ω_ez_e=88.08 cm^-1,B_e=21.22 cm^-1,a=0.785 cm^-1;B¹S⁺态:ω_e=1131.37 cm^-1,ω_ex_e=17.28 cm^-1,B_e=3.96 cm^-1,a_e=0.0215 cm^-1,C¹P态:ω_e=2696.37 cm^-1,ω_ex_e=73.43 cm^-1,B_e=15.91 cm^-1,a_e=0.776 cm^-1,D¹S⁺态:ω_e=3104.22 cm^-1,ω_ex_e=118.92 cm^-1,B_e=17.25 cm^-1,a_e=0.992 cm^-1,拟合结果与实验值吻合的较好.     

Pu3体系的结构与势能函数

用相对论有效原子实势(RECP)和密度泛函(B3LYP)方法对Pu_n(n=2,3)体系的结构进行了优化,得到了Pu₂和Pu₃分子的几何构型分别为D_∞h,D_3h,其基态分别为13和19重态.在B3LYP/RECP水平上得到Pu₂分子的光谱常数ω_e=52.3845cm^-1,ω_e　χ_e=0.02 关键词： 2')" href="#">Pu₂ 3')" href="#">Pu₃ 分析势能函数     

高频引力波对环形波导中电磁波的调制作用

讨论了垂直入射的、频率为ω_g的平面高频引力波对环形波导管中频率为ω_e的电磁波的调制作用．一般情况下，在波导管中与引力波传播方向垂直的对称平面附近，电磁波的能流密度会出现三种新的频率成分（2ω_e±ω_g）和ω_g．在ω_g》ω_e时，能流密度振幅的相对调制量与引力波的无量纲振幅h₀数量级相同．特别是当ω_g，ω_e和电磁波绕波导传播的绕行频率ω₀满足关系ω_g＝2ω_e》ω₀时，由于类似于共振的机制，能流密度会出现比h₀大几个数量级的振幅相对调制量．这个结果不会由于参数的微小改变而消失，这对于探测极微弱的引力辐射信号将是十分重要的 关键词：     

XY(H,Li, Na)分子基态的结构与势能函数

运用群论及原子分子反应静力学方法，推导了XY(H，Li，Na)分子基态的电子态及相应的离解极限.并采用密度泛函方法(B3LYP)和二次组态相互作用方法(QCISD)优化计算了XY(H，Li，Na)分子基态的平衡结构、振动频率和离解能.使用QCISD/6-311++G(3df,3pd)方法，对XY(H，Li，Na)分子基态进行了单点能扫描计算，采用最小二乘法拟合Murrell-Sorbie函数得到了相应的势能函数和与该基态相对应的光谱常数(B_e,α_e,ω_e和ω_eχ_e)，计算结果与实验数据符合得相当好. 关键词： 组态相关方法 基态 势能函数     

理论研究BeS(X~1∑~+)的光谱常数及分子常数

采用Davidson校正的内收缩多参考组态相互作用方法（MRCI+Q）结合相关一致五重基cc-pV5Z在二阶Douglas-Kroll Hamiltonian近似下,计算了BeS分子X¹∑⁺态的势能曲线.对势能曲线进行核价相关效应修正计算,得到了同时含有核价相关效应修正及相对论效应的势能曲线.拟合修正的势能曲线,获得BeS（X¹∑⁺）的光谱常数R_e,ω_e,ω_ex_e,ω_ey_e,B_e,α_e,β和D₀,分别为:0.17429 nm,997.06cm^-1,6.1056 cm^-1,0.0041 cm^-1,0.7893 cm^-1,0.006657 cm^-1,6.8002×10^-9cm^-1和4.2609 eV.与已有的实验结果及其它理论结果的比较表明,本文BeS（X¹∑⁺）的光谱常数的计算结果达到了较高的精度.通过求解双原子分子核运动的径向Schr（o|¨）nger方程,找到了非转动BeS（X¹∑⁺）的前40个振动态.针对每一振动态还分别计算了相应的振动能级、惯性转动常数和离心畸变常数等分子常数.     

Spectroscopic parameters and molecular constants of HI(X~1Σ~+),DI(X~1Σ~+) and TI(X~1Σ~+) isotope molecules

The potential energy curve (PEC) of HI(X¹Σ⁺) molecule is studied using the complete active space self-consistent field method followed by the highly accurate valence internally contracted multireference configuration interaction approach at the correlation-consistent basis sets, aug-cc-pV6Z for H and aug-cc-pV5Z-pp for I atom. Using the PEC of HI(X¹Σ⁺), the spectroscopic parameters of three isotopes, HI(X¹Σ⁺), DI(X¹Σ⁺) and TI(X¹Σ⁺), are determined in the present work. For the HI(X¹Σ⁺), the values of D₀, D_e, R_e, ω_e, ω_eχ_e, α_e and B_e are 3.1551 eV, 3.2958 eV, 0.16183 nm, 2290.60 cm^-1, 40.0703 cm^-1, 0.1699 cm^-1 and 6.4373 cm^-1, respectively; for the DI (X¹Σ⁺), the values of D₀, D_e, R_e, ω_e, ω_eχ_e, α_e and B_e are 3.1965 eV, 3.2967 eV, 0.16183 nm, 1626.8 cm^-1, 20.8581 cm^-1, 0.0611 cm^-1 and 3.2468 cm^-1, respectively; for the TI (X¹Σ⁺), the values of D₀, D_e, R_e, ω_e, ω_eχ_e, α_e and B_e are of 3.2144 eV, 3.2967 eV, 0.16183 nm, 1334.43 cm^-1, 14.0765 cm^-1, 0.0338 cm^-1 and 2.1850 cm^-1, respectively. These results accord well with the available experimental results. With the PEC of HI(X¹Σ⁺) molecule obtained at present, a total of 19 vibrational states are predicted for the HI, 26 for the DI, and 32 for the TI, when the rotational quantum number J is equal to zero (J = 0). For each vibrational state, vibrational level G(?), inertial rotation constant B_? and centrifugal distortion constant D_? are determined when J = 0 for the first time, which are in excellent agreement with the experimental results.     

AsCl自由基的基态及激发态的势能函数与光谱常数的研究

利用原子分子反应静力学推导出AsCl自由基的基态及激发态的理解极限. 采用完全活性空间自洽场和含Davidson 修正的内收缩多参考组态相互作用理论方法, 在aug-cc-pV5Z基组下对AsCl自由基进行结构优化计算及单点能扫描计算. 在AsCl自由基基态势能曲线的基础上, 通过Molcas程序拟合出了AsCl的光谱常数D_e, R_e, ω_e, ω_eχ_e, B_e 和α_e. 通过求解双原子分子核运动的径向Schrödinger方程, 找到了J=0 时该分子基态存在的40个振动态. 针对每一振动态, 计算了其振动能级、转动惯量B_ν和离心畸变常数D_ν, 与现有的实验及其他理论相比较, 本文的光谱参数和分子常数结果更准确. 关键词： AsCl 势能函数 光谱常数     

Spectral linewidth and FM response for a four-section DBR laser

Conclusion Theoretical expressions were presented for the spectral linewidth, effective linewidth enhancement factor and FM response of a DBR laser with two active and two passive sections. It was shown that a nearly flat red-shifted FM response over several gigahertz can be obtained by nonuniform current injection and modulation of the lower-carrier-density section in the active region. However, a high FM efficiency is also accompanied by a relatively large spectral linewidth. Wavelength tuning by using the injection currents through the passive sections enhances the red-shifted FM efficiency but also broadens the spectral linewidth. In practice, linewidth broadening could be suppressed by using a large-bandgap material as the passive waveguide in order to reduce the optical confinement factor and, consequently, the tuning efficiency.     

钙钛矿Mn基氧化物的电子顺磁共振行为的实验研究

借助电子顺磁共振技术,对Mn³⁺/Mn⁴⁺=2∶1和1∶1的两个典型体系 在居里温度T_C以上温区的顺磁行为进行了实验研究.实验表明,存在一特征温度 T_min,通过该温度将T_C以上的磁行为分成两个明显可区分的温区： 在T_min以上,共振谱由一对称的单线构成,Lande 因子g值与温度无关且接近 自由电子的值(～20023),线宽随温度呈线性变化等;而在T_{min关键词： 稀土锰氧化物 电子顺磁共振 交换变窄 自旋-自旋相互作用 自旋-晶格相互作用}     

Influence of Diffusion Parameters on the Spectral Characteristics of Raman Modes of Titanium-Diffused Lithium Niobate Planar Waveguides

ABSTRACT

A systematic investigation on the influence of the diffusion parameters (time and temperature) and initial titanium film thickness on the spectral characteristics of the LiNbO₃ Raman modes is reported. Raman spectra are measured in the range 50–1000 cm^?1 ～2 µm below the surface of the crystals. Broadening of the Raman lines and, therefore, crystal lattice disorder induced by the titanium ions are found to depend on the fabrication parameters. The disorder associated with the titanium ions near the surface of LiNbO₃ is encoded in the broadening of the A₁(TO₁) Raman line. A linear relation between the A₁(TO₁) mode broadening and the Ti concentration is presented. The diffusion theory is used to explain the experimental data. Raman spectroscopy combined with diffusion theory can be used to estimate the evolution of the titanium surface concentration.     

Widely tunable narrowband soliton source generation in tellurite microstructured fibers

We demonstrate widely tunable soliton and dispersive wave source generation in a highly nonlinear tellurite microstructured fiber pumped by a 1550 nm femtosecond fiber laser. The spectral range covered by the soliton and dispersive wave source is as wide as 1100 nm from 1150 to 2250 nm. It is shown that the spectral linewidth of the soliton and dispersive wave can be controlled by changing the length of the tellurite microstructured fiber easily owing to the dispersion-induced pulse broadening effects. This light source using tellurite microstructured fiber could open wide applications.     

Numerical analysis of stimulated Brillouin scattering in high-power double-clad fiber lasers

A theoretical analysis of stimulated Brillouin scattering (SBS) in linear cavity Yb³⁺-doped double-clad fiber lasers is presented by solving the steady-state rate equations with the SBS. The effects of cavity length, fiber core diameter, input mirror reflectivity at Stokes wavelength, Yb³⁺ concentration and laser linewidth on the SBS are discussed. Numerical results show that the SBS threshold power can be improved by shortening the cavity length, using large mode area fiber, reducing the input mirror reflectivity at Stokes wavelength, lowering the Yb³⁺ concentration and broadening the laser linewidth, and the influence of the laser linewidth on the SBS threshold power is more noticeable than other system parameters.     

Contributions to the Gaussian Line Broadening of the Proxyl Spin Probe EPR Spectrum Due to Magnetic-Field Modulation and Unresolved Proton Hyperfine Structure

A simple expression is derived to compute the total Gaussian linewidth of a Voigt line that is broadened by sinusoidal magnetic-field modulation as follows: ΔH^G_pp(H_m)²= ΔH^G_pp(0)²+ κ²H²_m, where ΔH^G_pp(H_m) is the Gaussian linewidth observed with an modulation amplitudeH_m/2 and ΔH^G_pp(0) is the Gaussian linewidth in the limit of zero modulation. The field modulation contributes an additional Gaussian broadening of κH_m, where κ is a constant, which adds in quadrature to ΔH^G_pp(0) to give the total Gaussian linewidth. Denoting the overall linewidth of the Voigt line in the absence of modulation broadening by ΔH⁰_pp(0), it is shown, both by analytical means and by spectral simulation, that the constant κ is equal to 1/2 in the limit ofH_m ΔH⁰_pp(0); however, using values ofH_mas large as ΔH⁰_pp(0) leads to only minor departures from κ = 1/2. The formulation is valid both for Lorentzian and Voigt lines and is tested for 2,2,5,5-tetramethylpyrrolidin-1-oxyl-3-carboxylic acid (3-carboxy proxyl) in CCl₄and in aqueous buffer. This spin probe was studied because the proxyl group is the only major spin-probe moiety whose Gaussian linewidth had not been characterized in the literature. For 3-carboxy proxyl, it is found that ΔH^G_pp(0) = 1.04 ± 0.01 G independent of solvent polarity. Precision values of the¹⁴N hyperfine coupling constant for 3-carboxy proxyl at 9.5°C are as follows: 14.128 ± 0.001 G in CCl₄and 16.230 ± 0.002 G in aqueous buffer. The temperature dependence of ΔH^G_pp(0) and the¹⁴N hyperfine coupling constant are reported as empirical equations. Results of the present work taken together with previously published data permits accurate correction for the effects of inhomogeneous broadening due to unresolved hyperfine structure and modulation broadening for the majority of spin probes in common use.     

Filling of the 3d band of the manganese in GdAl2−xMnxforx < 0.2

X-ray, magnetic, electrical resistivity and ESR studies of GdAl_2?xMn_x compounds were performed. The transition temperatures, effective mass, thermal broadening of resonance linewidth and g-factors were obtained. For low concentration of GdMn₂ in GdAl₂ up to 20%, Mn is nonmagnetic. Increasing of the effective mass and the thermal broadening linewidth ESR with increasing x can be explained by the presence of d-electrons.     

关于光激射器的线宽

本文从描述光激射器工作的基本方程出发,讨论了光激射器光束线宽的“短期”(short-time)部分。通常都以下式描写这部分线宽:△v_s=(8πhv(△v′)²)/P,(1)其中△v′是谐振腔电磁模的半宽度;v为光束频率;P为输出功率。我们的主要结论可以归结为以下三点:(1)线宽主要是由与电磁模耦合的耗散体系引起的,与分子耦合的耗散体系的贡献是可以忽略的;(2)在单模近似下,只要分子的线宽比电磁模的线宽大得多,则(1)式是正确的;(3)如果多模谐振腔中激发模与其他模之间的相互作用是强的,则式(1)将被推广为 △v_s=(8πhv(△v′)²)/P+(4hv(△v′))/P somefromn=(λ′≠λ)(r_λλ′²/(rλ′),(2) 其中r_λλ′是相关弛豫系数;r_λ′是模λ′的线宽。在某些情况下,式(2)中第二项可以比其第一项还大。所以,这可能是目前关于线宽的实验结果与由式(1)计算结果不相符合的原因之一。     

Determination of the Electron Density in an Argon Laser Plasma by Spectroscopy of the Hydrogen Hα and Hβ Lines

From measurements of the H_α and H_β spectral line profiles in a plasma, a method is developed which allows to separate the contributions of Doppler and Stark broadening. This method is superior to the deconvolution of Voigt profiles, in particular, when the lines are of low intensity. The electron density in the plasma can be calculated from the Stark broadening. An example is the low pressure (p ≈ 1 hPa) arc discharge of argon ion lasers which is characteristised by electron densities of approximately 10¹⁴ cm^?3 at heavy particle temperatures of about 10⁴ K. These plasma parameters lead to a broadening of the Balmer H_α and H_β spectral lines of hydrogen, which has a low concentration within the discharge area. The spectral lines are broadened due to the electron density dependent Stark effect and the temperature responsive Doppler effect. The results are consistent with predictions of the argon ion laser modelling.     

Magic Angle-Oriented Sample Spinning (MAOSS): A New Approach toward Biomembrane Studies

The application of magic angle sample spinning (MAS) NMR to uniformly aligned biomembrane samples is demonstrated as a new general approach toward structural studies of membrane proteins, peptides, and lipids. The spectral linewidth from a multilamellar lipid dispersion is dominated, in the case of protons, by the dipolar coupling. For low-γ or dilute spins, however, the chemical shift anisotropy dominates the spectral linewidth, which is reduced by the two-dimensional order in a uniformly aligned lipid membrane. The remaining line broadening, which is due to orientational defects (“mosaic spread”) can be easily removed at low spinning speeds. This orientational order in the sample also allows the anisotropic intermolecular motions of membrane components (such as rotational diffusion, τ_c= 10⁻¹⁰s) for averaging dipolar interactions to be utilized, e.g., by placing the membrane normal parallel to the rotor axis. The dramatic resolution improvement for protons which are achieved in a lipid sample at only 220 Hz spinning speed in a 9.4 T field is slightly better than any data published to date using ultra-high fields (up to 17.6 T) and high-speed spinning (14 kHz). Additionally, the analysis of spinning sidebands provides valuable orientational information. We present the first¹H,³¹P, and¹³C MAS spectra of uniformly aligned dimyristoylphosphatidylcholine (DMPC) bilayers. Also,¹H resolution enhancement for the aromatic region of the M13 coat protein reconstituted into DMPC bilayers is presented. This new method combines the high resolution usually achieved by MAS with the advantages of orientational constraints obtained by working with macroscopically oriented samples. We describe the general potential and possible perspectives of this technique.