PbCl_2分子的光解离

用YAG激光的四次谐波光解离PbCl_2分子。实验确认了这种光解过程是双光子过程。通过对激光诱导荧光的测量,发现这一光解过程造成了Pb原子的亚稳态6p~2~3P_2与基态6p~2~3P。间的粒子数反分布。同时观察到基于6p~2~3P_2能级的受激共振辐射及受激喇曼散射。     

碰撞对受激Raman散射的影响

从动力学方程出发，引入有效碰撞，讨论了碰撞对受激Raman散射线性增长率的影响.结果表 明，碰撞阻尼和Landau阻尼使得受激Raman散射线性增长率有了实质性的下降，受激Raman散 射只能发生在电子温度和电子密度平面的一个有限区域.现在的理论模型能够解释受激Raman 散射光谱上存在的“缝”(gap)现象. 关键词： 受激Raman散射 碰撞阻尼 线性增长率     

PbCl2分子的光解离

用YAG激光的四次谐波光解离PbCl₂分子。实验确认了这种光解过程是双光子过程。通过对激光诱导荧光的测量,发现这一光解过程造成了Pb原子的亚稳态6p^{2 3}P₂与基态6p^{2 3}P。间的粒子数反分布。同时观察到基于6p^{2 3}P₂能级的受激共振辐射及受激喇曼散射。 关键词：     

密集波分复用石英光纤通信系统中受激Raman散射的稳态分析模型

假设石英光纤的Raman增益谱为线性谱,并给出了拟合直线.以此为基础,得到了前向N信道 受激Raman散射稳态耦合波方程的解析解.这个解析解是在考虑了N个信号光之间串话下得到 的,它适用于任意功率大小的信号光和任意信道间隔排列的情况.N个信号光在石英光纤中经 过受激Raman散射作用后,具有以下特点：在传输过程中,任意两信道的信号光光子通量的比 值随光纤的有效互作用长度、总的输入光子通量和两信道频率间隔按指数规律变化.解析解 与数值解进行了比较,两者取得了很好的一致. 关键词： 受激Raman散射 密集波分复用 石英光纤 Raman放大     

水中受激拉曼散射的能量增强及受激布里渊散射的光学抑制

为提高液体介质中受激拉曼散射的输出能量,提出了通过温度调控来抑制受激布里渊散射的方法,设计了532 nm多纵模宽带脉冲激光泵浦的受激拉曼散射发生系统,测量了不同温度下水中前向受激拉曼散射及后向受激布里渊散射的输出能量,分析了水温、泵浦激光线宽及热散焦效应对受激拉曼散射输出能量影响的物理机制.实验结果表明:通过降低水温可实现对受激布里渊散射过程的有效抑制,同时减小热散焦效应带来的光束畸变,从而有效提高受激拉曼散射的输出能量.研究结果对液体介质中的受激拉曼散射多波长转换具有重要意义.     

单模石英光纤中连续波泵浦SRS谱的演化

利用连续波掺Yb双包层光纤激光器为泵浦源,对单模石英光纤中受激Raman散射谱的形成过程进行了实验研究结果表明,由自发Raman散射向受激Raman散射演化的过程中Stokes谱宽度不断变窄当Stokes波信号功率较强时,在Raman光谱内部会出现能量红移现象,使Stokes光谱峰值相对于泵浦波的频移量从440cm^-1转化到490cm^-1.     

受激热散射基本概念及理论描述

吸收热对固体激光器输出光束质量的影响及受激热散射在高能应用中与受激布里渊散射的激烈竞争已越来越引起人们的关注,然而国内对此问题的研究尚少见报道。本文给出受激热散射的理论描述并着重澄清关于受激热散射的几个基本概念。     

三角激光脉冲尾波加速粒子模拟

电子俘获是激光尾波场加速电子的主要机理，增大电子的初速度可以使更多的电子被尾波场俘获.提出三角脉冲激发尾波加速电子的方案，三角脉冲平缓上升沿激发受激Raman散射，用以初步加速电子，三角脉冲陡峭下降沿激发尾波场，将更多的电子加速到接近光速.2D3V粒子模拟结果证实了这一点.同时表明：脉冲长度为几个等离子体波长的超强激光在稀薄等离子体中传播时，还激发侧向Raman散射.在侧向受激Raman散射中，静电波增长最快的波矢模式为k_p=(2ω_p/ω₀ 关键词： 有质动力 电子俘获 前向受激Raman散射 侧向受激Raman散射     

带受激布里渊散射池的位相共轭激光器输出的空间特性

本文应用传输矩阵的方法对受激布里渊散射位相共轭腔输出的空间特性进行了分析及编程计算，给出了各种参数下受激布里渊散射－位相共轭腔的传输光束轮廓图，同时给出了实验结果与之相比较，提出了设计受激布里渊散射共轭腔时应注意的问题及几种实用的受激布里渊散射位相共轭腔的腔型。     

超短超强激光与气体靶相互作用中的背向受激Raman散射

 实验诊断测量了超短超强激光与气体靶相互作用产生的背向受激Raman散射,在实验条件下呈现强耦合模式,背向受激Raman散射出现非线性Stokes多峰伴线结构,峰值的频率间隔小于等离子体波的频率,可以大致地推断出激光打靶过程中产生的等离子体密度偏低,其结果与等离子体强耦合理论计算结果一致。     

Threshold and conversion experiments on seeded stimulated Raman scattering

High energy-conversion efficiencies in Stimulated Raman Scattering (SRS) are demonstrated both in experiments and by simulations for pump powers below SRS threshold. The scattering is induced by a short seed pulse at the Stokes frequency, the pulse width of which is much shorter than the pump pulse width and which is comparable with the medium's dephasing time.     

Time—dependent Theory of Raman Scattering with Pulses—Application to Continuum Raman Spectroscopy

A theory of real-time dependence of Raman scattering for a pulse-mode laser is developed within second-order perturbation theory and using the wavepacket terminology.We apply the theory to continuum Raman scattering for short and long pulses and varying pulse carrier frequency,For an initial ground virational state,it is shown that the rate of Raman emission as a funcition of time and pulse carrier frequency is structureless for all pulses,and for pulses that are longer than the dissociation time the rate also decays with the pulses.This is contrary to recently reported resonance fluorescence type structures at long times (M.Shapiro,J.Chem.Phys.99,2453(1993),We explain why such structures are unphysical for continuum Raman scattering.     

Generation of undamped stokes radiation under resonant pumping of the dipole-forbidden transition in a Ξ-atom

We have developed a theory of the nonlinear ring interaction of three intense fields in the scheme of resonant Raman scattering on the dipole-allowed transition from the ground state to the first excited state of a cascade three-level quantum system. We show that the backward Stokes radiation generated by a pump resonant to the dipole-forbidden transition can be used in remote laser sensing of metal vapors.     

Charge transfer effects in surface enhanced Raman scattering

Surface enhanced Raman scattering (SERS) due to charge transfer interactions between the adsorbed molecule and the metal surface is analyzed using the semiempirical Wolfsberg-Helmholz method¹ to relate the molecule-surface interactions and the resulting charge transfer states to the overlap integrals between the metal conduction-band orbitals and an acceptor or donor molecular orbital of the molecule. Calculations for the model system of ethylene adsorbed on silver (approximated as a simple cubic metal with tight binding wave functions constructed from Ag 5s valence orbitals), with charge-transfer excitation of an electron from the metal to the antibonding ethylene π orbital, show that charge-transfer Raman enhancements of the order of 10 to 1000 are possible if the charge-transfer band is partially resonant with the exciting radiation. The net enhancement is the product of the charge-transfer gain and the electrodynamic enhancement due to plasmon resonances at surface roughness elements. Symmetric vibrations usually will be enhanced substantially more than nonsymmetric ones by charge-transfer because, in contrast to non-resonant Raman scattering, the vibrational coupling is primarily Franck- Condon (due to differences in the equilibrium nuclear configurations of the ground and excited charge transfer states and the resulting nonorthogonality of different vibrational sublevels of these states) rather than Herzberg-Teller (due to vibrationally induced changes in the electronic wave functions). The charge-transfer mechanism is selective with the most enhanced vibrations involving those atoms which experience the greatest change in electron density between the ground and excited charge-transfer state. A recent report of SERS for benzene on platinum,² strongly suggests charge-transfer enhancement because the electromagnetic-field-enhancing plasmon resonances are strongly damped in this metal.The complete paper will be published in the December 1, 1982 issue of the Journal of Chemical Physics.     

Effective sideband cooling in an ytterbium optical lattice clock

Sideband cooling is a key technique for improving the performance of optical atomic clocks by preparing cold atoms and single ions into the ground vibrational state. In this work, we demonstrate detailed experimental research on pulsed Raman sideband cooling in a $^{171}$Yb optical lattice clock. A sequence comprised of interleaved 578 nm cooling pulses resonant on the 1st-order red sideband and 1388 nm repumping pulses is carried out to transfer atoms into the motional ground state. We successfully decrease the axial temperature of atoms in the lattice from 6.5 μK to less than 0.8 μK in the trap depth of 24 μK, corresponding to an average axial motional quantum number $\langle n_z\rangle<0.03$. Rabi oscillation spectroscopy is measured to evaluate the effect of sideband cooling on inhomogeneous excitation. The maximum excitation fraction is increased from 0.8 to 0.86, indicating an enhancement in the quantum coherence of the ensemble. Our work will contribute to improving the instability and uncertainty of Yb lattice clocks.     

双折射光纤受激拉曼散射偏光特性的实验研究

对椭圆芯光纤受激拉曼散射偏光特性进行了系统的实验研究。实验巾观察到8级斯托克斯线和2级反斯托克斯线,对不同偏振态的抽运光激励下各级斯托克斯线的偏振特性、拉曼频移等参量进行了分析,并给出了经验公式。其结果与实验数据符合良好。实验表明,双折射光纤受激拉曼谱的各级斯托克斯线的偏振状态不但与拉曼介质有关还与抽运光的偏振态有关,入射抽运光偏振态对低阶次的斯托克斯线拉曼频移的影响较小,而对高级斯托克斯线拉曼频移影响较大。     

Disturbing interference patterns in femtosecond stimulated Raman microscopy

Femtosecond stimulated Raman microscopy (FSRM) is an upcoming technique in nonlinear microscopy which facilitates rapid chemical mapping. It employs femtosecond white‐light pulses as probe pulses and intense picosecond pulses as pump pulses. Stimulated Raman scattering (SRS) occurs at the focus of a scanning microscope. Chemical constituents in the sample are identified via their Raman signatures. In this article, disturbing interference patterns in FSRM are reported. They are caused by a broadening of the pump pulse due to nonlinear interactions in the focal region of the microscope and reduce the signal‐to‐noise ratio. The properties of these modulations are explored, and the methods to suppress them are presented. Copyright © 2009 John Wiley & Sons, Ltd.     

Determination of the spectral width of Raman gain regions for different far infrared laser gases using a metal mesh Fabry Pérot interferometer

In this paper we report on the determination of the spectral width of Raman gain regions for different far infrared laser gases using a metal mesh Fabry Pérot interferometer. By use of broadband pump radiation emitted from a high pressure CO₂ laser we generated far infrared radiation within the Raman gain regions via stimulated Raman scattering. The spectral width of the far infrared radiation was determined using a Fabry Pérot interferometer in high interference order. We applied the method to study stimulated Raman scattering in D₂O and methylfluoride at different gas pressures.     

Numerical simulations of pulsed and quasi-cw regimes of synchronously pumped Raman oscillators

Synchronously pumped Raman oscillators allow for an efficient frequency conversion of pump pulses whose power is well below the threshold for extracavity stimulated Raman scattering (SRS). Numerical simulations show that the cavity mismatch of pump laser and Raman oscillator is critical for maximum conversion efficiency and minimum pulse duration for transient and stationary SRS. At a certain mismatch the simulations predict a quasi-cw Raman oscillator output even at moderate cavity quality factors. Optimum operation conditions are discussed for pump pulse trains of finite lengths. The results of the numerical calculations are in qualitative agreement with a simple phenomenological model. PACS 42.55.Ye; 42.65.Dr; 42.55.Lt     

高阶色散对高双折射光纤增益谱的影响

根据参量放大和拉曼效应共同作用下的耦合波方程,在考虑高阶色散情况下,当输入泵浦波偏振方向同双折射轴成45时,通过引入拉曼增益的洛伦兹模型,研究了高双折射光纤中,参量放大和拉曼效应共同作用下的增益谱随相关参量的变化关系。结果表明:高双折射光纤中,在不同色散区,不同的输入参量（输入功率、群速度失配等）条件下,参量放大和拉曼效应共同作用下的增益谱受到高阶色散的影响,增益谱的结构、强度和谱宽产生了变化, 高阶色散对增益谱的影响不可忽略;可以利用增益谱在大群速度失配区域远离中心频率偏移的性质,提取T频率脉冲。