基于回波信号仿真的瑞利-喇曼-米激光雷达研制

 在分析瑞利、喇曼和米散射仿真回波信号的基础上,研制了一台探测大气温度、气溶胶和卷云的瑞利-喇曼-米散射激光雷达,实现了一台激光雷达针对大气温度、气溶胶和卷云光学特性的多参数探测。为提高瑞利和喇曼微弱回波信号信噪比,采用了极高灵敏度的R4632光电倍增管和光子计数技术;为实现对大气气溶胶和卷云的探测,532 nm回波信号采取高低分层技术、高层通道回波衰减方法和探测器门控技术。瑞利-喇曼-米散射激光雷达的探测结果证明了利用仿真回波信号指导激光雷达设计的可行性。     

部分离化激光等离子体的受激喇曼散射不稳定性

由于部分离化激光等离子体中存在束缚电子，它可显著改变其参量不稳定性。本文分析了部分离化激光等离子体的受激喇曼散射的非线性色散关系，计算了钕玻璃倍频和三倍频激光受激喇曼散射的增长率，结果表明，前向受激喇曼散射显著增强，后向受激喇曼散射影响不大。     

结晶紫、碱性品红、染料1555吸附在银胶上的表面增强喇曼散射的激发波长关系

本文通过研究在不同激发波长下吸附在银胶上的结晶紫、碱性品红、染料1555的表面增强喇曼散射散射强度的变化,分析了普通喇曼散射、表面增强喇曼散射及表面增强共振喇曼散射之间的联系与不同。     

全天时喇曼激光雷达探测大气水汽的技术实现及分光系统设计

为实现大气水汽的全天时测量,选用Nd∶YAG脉冲激光器的四倍频输出266.0nm作为激励光源,设计日盲紫外域喇曼激光雷达系统.由于低层大气污染造成的臭氧污染,通过增加大气氧气的振动喇曼散射信号测量通道,实时反演近地表臭氧浓度的分布,为修正激光雷达方程中的臭氧吸收提供解决方案.同时,选用高光谱分辨率光栅和窄带宽激光反射镜设计光栅光谱仪作为激光雷达的分光系统.仿真计算表明,入射角为10°时,设计的光栅光谱仪可有效分离并提取氧气、氮气和水汽的振动喇曼散射回波信号,日盲紫外喇曼激光雷达系统可实现全天时状态下2km高度范围内大气水汽的廓线探测.     

稀土配合物的喇曼散射和超喇曼散射效应

以可见光为激发光,观测了稀土配合物的喇曼散射和超瑞利、超喇曼散射光谱,简单论述了超瑞利和超喇曼散射的理论,对实验测出的谱线进行了认证与分析     

LiZnTa_3O_9晶体的喇曼光谱及其对称性

本文首次获得了LiZnTa_3O_9晶体的喇曼光谱,并与LiTaO_3的喇曼光谱进行了比较.前向喇曼散射表明此晶体不存在极化声子色散,从而断定其对称性是D_(3d)点群,然后对LiZnTa_3O_9的喇曼光谱进行了识别和讨论.     

固体的光散射讲座 第四讲 非线性喇曼散射

非线性喇曼散射是指由于分子的偶极矩或激活介质的宏观极化矢量与光电场强度呈非线性关系,所引起的喇曼散射过程.在自发散射过程的理论描述中,振动着的分子体系的偶极矩可以写成其中q为分子振动的简正坐标,u为分子体系的固有偶极矩,α(q)称为分子体系的极化率,β(q)等则可称为超极化率.显然,上式中第二项所引起的喇曼散射是线性的,第三项以后各项所引起的喇曼散射则属于非线性的,其中由β(q)所引起的喇曼散射则称为超喇曼散射[1,2] 当人射光较弱时,自发的线性及非线性喇曼散射效应都非常弱,而且它们是非相干的散射.当人射的泵浦光较强时,再…     

激光等离子体诊断用的可见光探针

一、引言 激光可见光探针是激光等离子体研究中有效的诊断工具,能达到很高的时空分辨率。在钕玻璃激光打靶实验中,通常采用从打靶光分出一部分经倍频和受激喇曼前向散射来得到可见光探针。倍频和散射过程使光脉冲得到了压缩,但是,受激喇曼前向散射的压缩性     

XeCl准分子激光在铅蒸气中的受激喇曼散射

研究了XeCl准分子激光在铅蒸气中的喇曼散射的输出能量及转换效率的参数依赖关系,得到能量～120mJ、峰值功率～2MW的喇曼光输出脉冲.观察到喇曼光脉冲波形上的多峰结构,并将其归因于喇曼散射中的合作效应.     

光纤中的紫外受激喇曼散射

用YAG∶Nd激光的三次谐波作激励光,我们在光纤维中观测了紫外受激喇曼散射。测定了受激喇曼散射的峰值波长,它们是3610(?)、3722(?)和3791(?)。指出了各受激喇曼线相应的散射元.     

在单模光纤中放大的反斯托克斯拉曼背向自发散射的温度效应

在单模光纤中,输入的激光功率大于阈值时．出现放大的反斯托克斯拉曼背向自发散射现象。实验发现：放大的反斯托克斯拉曼背向自发散射具有温度效应．与反斯托克斯拉曼背向自发散射一样,放大的拉曼散射光的光子通量受到光纤温度的调制。反斯托克斯拉曼背向白发散射的放大效应抑制了单模光纤中的相干噪声,改善了系统的信噪比。实验还发现．放大的反斯托克斯扎曼背向自发散射空域曲线上放大的端点位置随激发功率的增高前移并具有一定的规律性。放大的反斯托克斯拉曼背向自发散射的温度效应作为一种新的测温原理,已应用于远程30km分布光纤温度传感器系统。     

Spontaneous Raman scattering: a useful tool for investigating the afterglow of nanosecond scale discharges in air

Nanosecond scale discharges are considered an interesting way for assisting combustion by enhancing either flame stabilization or ignition. Better understanding of energy deposit and radical species production processes is still required under pressure conditions normally encountered in combustion. The purpose of the present paper is to show that spontaneous Raman scattering, seldom used to investigate nanosecond pulsed discharges, is a useful measurement method for investigating the energy deposit of these discharges. The advantage of spontaneous Raman scattering is described by analyzing N₂ and O₂ spectra during the post-discharge of a filamentary nanosecond air discharge under atmospheric pressure, using phase-locked average spectra. The main advantages of spontaneous Raman scattering measurements are that they allow line-wise probing of different species with the same experimental setup and the determination of vibrational distribution by comparison with theoretical modeling over a wide range of vibrational levels (from v=0 to v=20 for N₂). The model proposed takes into account the high level of vibrational excitation and the strong non-equilibrium observed, allowing the characterization of the vibrational relaxation over the complete post-discharge duration. Although the rotational structure is not resolved, the rotational temperature and thus translational temperature are determined with a moderate uncertainty for T above 500 K.     

探测大气中CO2的Raman激光雷达

基于大气激光后向散射光谱，研究和设计了探测大气CO₂浓度的Raman激光雷达,其发射机采用Nd∶YAG激光的三倍频354.7nm作为工作波长,发射的单脉冲能量350mJ,重复频率20Hz；接收机采用了光电倍增管(量子效率25%)和光子计数器(计数速率200MHz),探测CO₂的Raman散射371.66nm(频移1285cm^-1)信号,(1小时累加)近地面2.5km以内信噪比不小于8.采用组合滤光片来抑制强的354.7nm Mie-Rayleigh后向散射和氧气375.4nm Raman后向散射对信号的严重干扰. 比较分别来自大气CO₂和参考气体N₂的Raman后向散射回波,可反演出大气中CO₂的相对浓度. 关键词： 大气光学 激光雷达 Raman散射光谱 参考气体 Mie-Rayleigh散射     

Picosecond stimulated Raman scattering in crystals

The comparative values of the peak and integral cross sections of spontaneous Raman scattering and the optical dephasing time of molecular vibrations were determined for several oxide crystals by spontaneous Raman spectroscopy. The spectral, time, and energy parameters of stimulated Raman scattering (SRS) were measured for ten crystals using picosecond YLF: Nd laser pumping with a radiation wavelength of 1047 nm. An analysis of the experimental dependence of the threshold energy of pumping SRS on the integral and peak cross sections of spontaneous Raman scattering showed that the SRS gain increment explicitly depended on the integral cross section and was independent of the peak cross section of spontaneous Raman scattering as the ratio between the pumping pulse width (11 ps) and the time of optical dephasing of molecular vibrations changed from 0.42 to 9.3. The gain coefficients of steady-state stimulated Raman scattering under threshold stimulated Raman scattering conditions were determined for all the crystals studied on the basis of the measured threshold SRS pumping energies, the duration and width of the spectrum of pulses, the nonlinear interaction length, the intensity of pumping, and the theoretical dependences that relate the steady-state and transient SRS gain increments. The steady-state SRS gain coefficients obtained in this work fitted well a linear dependence on the peak cross sections of spontaneous Raman scattering, which substantiated the correctness of our analysis and measurements.     

Stimulated Raman scattering and spontaneous Raman solitons in ammonia

In this study we report the first observation of spontaneous Raman solitons in stimulated Raman scattering (SRS) by the gas NH₃. The scattered radiation is called Stokes radiation. Raman solitons are of considerable interest, because their existence can be explained by quantum-mechanical fluctuations of the electromagnetic field in vacuum. We have observed spontaneous Raman solitons in a forward SRS configuration for two different molecular transitions of NH₃, the laser emissions at 58 μm and 72.6 μm wavelength. These are optically pumped by 10 μm CO₂-laser pulses with a duration of 100 ns and an energy of 150 mJ. Spontaneous Raman solitons are short spikes in the pump pulse which occur during its depletion. Their origin is the rapid π phase change of the Stokes seed. In contrast to other laboratories we have used single-pass cells. Thus, we have succeeded in observing multiple spontaneous Raman solitons during one pump pulse. Previous experiments with multi-pass cells never showed multiple solitons. Since multiple spontaneous Raman solitons have already been reported in an earlier experiment with a single-pass cell filled with hydrogen at high pressure, we conclude that such multiple Raman solitons can be observed mainly in this type of gas cell. Subsequently, we have performed statistical measurements on the delay time and the height of the spontaneous Raman solitons in the depleted pump pulse for the 58 μm-NH₃ emission. We have compared these statistics with theory and equivalent experimental results of other laboratories. They are in good agreement with the assumption that quantum-mechanical fluctuations are the origin of spontaneous Raman solitons. The most recent theories postulate that the origin of the formation of spontaneous Raman solitons can be explained by the rapid π phase change of the Stokes seed as well as that of the laser or polarization wave. Therefore, we have determined the phase of the spontaneous Raman solitons relative to the depleted pump pulse. Although, such changes of sign of the relative phase have already been observed in an earlier SRS experiment with hydrogen at high pressure, we did not detect any in our experiment. Therefore, we conclude that in this experiment the π phase change occurs in the Stokes or polarization wave.     

Production of pseudoscalar bosons upon stimulated Raman scattering in dielectric media

Conditions for the emergence of pseudoscalar vibrational excitations in the spectra of spontaneous and stimulated Raman scattering in molecular liquids and crystals are determined. The spectra of spontaneous and stimulated Raman scattering by pseudoscalar bosons are measured experimentally for several liquids and crystals.     

Raman response function of atmospheric air

A model of the full Raman response function of a gas mixture including rotational and vibrational motions of molecules is presented and is applied to examine the properties of the retarded optical nonlinearity of atmospheric air. For few-cycle laser pulses, broadband field waveforms, and/or high gas temperatures, both rotational and vibrational motions can significantly contribute to the Raman response of atmospheric air, with the ratio of the rotational and vibrational parts of the Raman response function controlled by the gas temperature and the temporal shape of the laser field.     

绝对探测大气温度的纯转动拉曼激光雷达系统

纯转动拉曼激光雷达是探测大气温度廓线的重要手段之一,其正常工作需要配置其他并行校正设备,制约其在气象及环境监测领域中的实用化进程.基于大气氮气分子的纯转动拉曼谱型对温度的依赖性,提出并设计了绝对探测大气温度廓线的纯转动拉曼激光雷达系统.系统采用波长532 nm且脉冲能量300 m J的激光激励源和口径250 mm卡塞格林望远镜的接收器,设计了衍射光栅和光纤Bragg光栅结合的多通道并行纯转动拉曼光谱分光系统;仿真分析氮气和氧气分子的纯转动拉曼散射谱线间关系,优化选择了6条氮气分子的纯转动拉曼谱线以直接反演大气温度,设计了两级滤光器间转接光纤阵列的结构;基于最小二乘原理推导了绝对探测大气温度的反演算法,并结合标准大气模型,分析了纯转动拉曼激光雷达绝对探测大气温度的探测性能.结果表明,所设计纯转动拉曼激光雷达系统可直接反演大气温度廓线,在测量时间17 min内,温度偏差小于0.5 K的探测高度达2.0 km.     

水汽探测拉曼激光雷达的新型光谱分光系统设计与分析

提出并设计了一套新型的大气水汽和气溶胶探测用紫外域拉曼激光雷达系统, 以二向色镜和超窄带滤光片构成高效率拉曼光谱分光系统, 实现激光雷达大气回波信号中米-瑞利散射信号、 氮气和水汽的振动拉曼散射信号的精细分离和高效率提取. 利用美国标准大气的分子散射模型和实测的大气米散射信号模型, 对分光系统的米-瑞利散射信号的抑制率、大气水汽测量的信噪比和误差进行数值仿真设计. 搭建实验系统对西安地区夜间的大气水汽进行实验观测, 并利用有云天气下实测的激光雷达回波信号, 反演获得大气后向散射比和水汽混合比的相关特性, 验证了该拉曼光谱分光系统对米-瑞利信号的抑制率达到10^-7以上量级. 理论和实验结果表明, 设计的新型拉曼光谱分光系统可以在大气后向散射比为17时, 实现水汽探测误差小于15%, 满足拉曼激光雷达系统对大气水汽的高效率探测. 关键词： 拉曼激光雷达 水汽混合比 大气后向散射比     

Enhanced raman scattering spectra for gaussian light beams

We show that effect of light-induced focusing of the low-frequency Raman scattering components and defocusing of the high-frequency components in the field of a gaussian exciting beam lead to a slight shift of the enhanced Raman line relative to the center of the spontaneous Raman line on the low-frequency side. We propose and provide a rationale for an efficient algorithm for calculating the average power for enhanced Raman scattering, based on numerical solution of the wave equation for the field of the Stokes beam developing from spontaneous Raman scattering. __________ Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 74, No. 2, pp. 230–236, March–April, 2007.