单模石英光纤中受激喇曼散射的研究

利用连续光纤激光器为泵浦源,对单模石英光纤中的受激喇曼散射进行了实验研究.在较低功率泵浦下,观察到由自发喇曼散射向受激喇曼散射演化的过程中,光谱不断变窄;当Stokes波信号功率较强时,观察到光谱峰值相对于泵浦波的频移量从440 cm－1转化到490 cm－1.在改进耦合系统后,不仅观察到一级喇曼频移,并且观察到了高阶Stokes光.在产生多级喇曼光谱时能量移动比较复杂,每两级的喇曼频移间隔并不完全相同.     

钡蒸气的受激喇曼散射及碰撞诱导受激辐射

在宽带XeCl激光泵浦的钡蒸气中,观察到波长分别为472.6nm,582.6nm和648.3nm的碰撞诱导受激辐射以及波长为475nm的受激喇曼散射.碰撞锈导受激辐射脉宽为3ns左右的自终止型短脉冲,其强度随缓冲气体压力的升高而上升.喇曼光脉冲前沿与泵浦光脉冲前沿之间有长20ns的时间延迟,喇曼转换效率随缓冲气体压力的升高而下降     

热散焦效应对甲烷后向受激喇曼散射的影响

采用单纵模Nd:YAG二倍频激光泵浦,研究了CH4气体中的受激喇曼散射．实验发现,当激光的重复频率为2 Hz,1．1 MPa CH4中,泵浦能量为95 mJ时,后向一级斯托克斯(BS1)的量子转化效率可达73％,并且由于激光脉冲的张弛振荡,BS1的脉宽被压窄到1．2 ns,峰值功率达到了泵浦光功率的2．7倍,其光束质量大大优于泵浦光．在同样条件下,而重复频率为10 Hz时,BS1的量子转化效率降低为36％,但对光束质量影响不大,这是因为BS1呈现为与泵浦光波前翻转的复制光波,可以补偿热畸变．研究结果表明,如果设计一个CH4／He混合气体的带封闭循环冷却系统的高性能630 nm喇曼激光器,可能有其实际应用价值．     

KGW晶体外腔式高功率579nm喇曼黄光激光器

报道了579nm高功率KGd(WO4)2喇曼晶体外腔式喇曼黄光激光器的输出特性.基于808nm脉冲激光二极管侧面泵浦Nd∶YAG陶瓷、腔内BBO电光晶体同步延迟调Q和Ⅰ类临界相位匹配的LBO晶体腔外倍频方案,并通过外腔式KGW晶体Ng轴二阶斯托克斯喇曼频移,获得了579.54nm黄光激光输出.当脉冲信号重复频率为1kHz、532nm泵浦光最高平均功率为5.02W、脉冲宽度为10.1ns时,获得了最高平均功率2.58 W、脉冲宽度7.4ns、峰值功率348.6kW的579.54nm二阶斯托克斯喇曼黄光激光输出;532nm至579.54nm的光-光转化效率为51.4%、斜率效率为54.8%,光束质量因子Mx2-579.54=5.829、My2-579.54=6.336,输出功率不稳定性小于±2.35%.实验表明:外腔式喇曼结构能够高效地获得喇曼黄光,具有很高的光-光转化效率及良好的功率稳定性,并通过脉冲LD结合同步延迟电光调Q可获得高重复频率、高平均功率、窄脉冲宽度和高峰值功率的黄光激光输出.     

宽频带聚焦泵浦准稳态受激电子喇曼散射的增益因子和能量转换效率

本文采用Raman-Maxwell-Bloch方程,计算了宽频带聚焦泵浦准稳态受激电子喇曼散射的增益因子和能量转换效率.在计算中考虑了泵浦抽空、喇曼介质对泵浦光的吸收和喇曼介质的泡和效应.计算结果与XeCl激光在钡蒸汽中的受激喇曼散射实验基本上符合.     

双折射光纤受激喇曼散射的研究

本文详细地研究了双折射光纤的受激喇曼散射.观测到9级斯托克斯受激喇曼谱.文中讨论和测试了阈值和频移与泵浦光偏振方向间的关系;当泵浦光偏振方向与光纤椭圆核的长轴或短轴平行时的传输损耗.并根据测得的阈值在理论上计算了各级斯托克斯线的喇曼增益系数.     

KGW 晶体外腔式高功率579 nm喇曼黄光激光器

报道了579 nm高功率KGd(WO₄)₂喇曼晶体外腔式喇曼黄光激光器的输出特性.基于808 nm脉冲激光二极管侧面泵浦Nd:YAG陶瓷、腔内BBO电光晶体同步延迟调Q和Ⅰ类临界相位匹配的LBO晶体腔外倍频方案,并通过外腔式KGW晶体Ng轴二阶斯托克斯喇曼频移,获得了579.54 nm黄光激光输出.当脉冲信号重复频率为1 kHz、532 nm泵浦光最高平均功率为5.02 W、脉冲宽度为10.1 ns时,获得了最高平均功率2.58 W、脉冲宽度7.4 ns、峰值功率348.6 kW的579.54 nm二阶斯托克斯喇曼黄光激光输出;532 nm至579.54 nm的光-光转化效率为51.4%、斜率效率为54.8%,光束质量因子M_x-579.54²=5.829、M_y-579.54²=6.336,输出功率不稳定性小于±2.35%.实验表明:外腔式喇曼结构能够高效地获得喇曼黄光,具有很高的光-光转化效率及良好的功率稳定性,并通过脉冲LD结合同步延迟电光调Q可获得高重复频率、高平均功率、窄脉冲宽度和高峰值功率的黄光激光输出.     

准分子激光束的喇曼组束

受激喇曼散射可以将紫外准分子激光辐射频移到特定的近紫外或可见光波长,采用喇曼整形技术可以改善斯托克斯光的光束质量,本文报道喇曼组束提高喇曼整形效率的实验结果.     

基于硅波导的喇曼光放大器

在硅波导上添加反向偏压的PIN结构,当波导产生受激喇曼散射时,可以将波导中双光子吸收(TPA)产生的光生自由载流子扫出波导,降低了波导的非线性损失,极大地提高了硅波导中泵浦光对信号光的喇曼增益。为了应用已经非常成熟的硅工艺,并且应用硅波导使器件小型化,根据法布里-帕罗(F-P)腔和行波放大器理论,在硅波导两端的解理面蒸镀增透膜,应用这种波导的喇曼效应设计了一种光放大器,即基于硅波导的喇曼光放大器。建立了计算放大器增益的方程,给出了不同波导长度和输入功率情况下的放大器增益,得出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。基于硅的光放大器有较高的饱和功率且没有泵浦源的限制,通过调整泵浦激光的波长可以放大不同波长的信号光。     

金属蒸气受激喇曼散射的原子基态抽空效应

将受激Raman散射原子基态及终态粒子数变化的速率方程与聚焦的泵浦光束及喇曼光束功率变化的微分方程组联立并进行数值求解;研究了金属蒸气受激Raman散射过程中基态粒子数的抽空现象及其对Raman能量转换过程的影响。     

多波长消荧光拉曼光谱仪的研制及应用研究

拉曼光谱技术作为探究分子、晶体及其结构特征的有力手段,具有快速、无损、样品用量小、无需前处理且适应性强等优点,已被广泛应用于食品安全、石油化工等领域。但在拉曼光谱应用中,常常受到荧光背景干扰,导致拉曼信号降低,严重的情况下拉曼信号甚至会淹没在荧光背景中。为解决拉曼技术在实际应用中荧光背景干扰的问题,从仪器角度出发,采用二色镜对多波长拉曼光谱进行光路耦合设计,研制了近红外拉曼光谱与移频差分拉曼复合一体的多波长消荧光拉曼光谱检测系统,其中近红外拉曼光谱采用1 064 nm激光光源设计,移频差分拉曼光谱选取784.5和785.5 nm两组激光光源进行时分复用,在移频差分拉曼光谱检测的同时,亦可获得两组单波长拉曼光谱数据。通过对比同步测试和分时逐次测试的强度及峰位稳定性,验证了多波长消荧光拉曼光谱仪的同步测试性能;选取了多种荧光背景强弱不同的样品,进行了单波长拉曼、近红外拉曼及移频差分拉曼光谱的对比分析。针对丙酮、乙腈等荧光背景较弱的样品,可采用单波长拉曼光谱对样品进行定量及定性分析;针对食用油、红色塑胶微粒等荧光背景与拉曼信号强度相当的样品,可采用近红外拉曼光谱对样品进行定量及定性分析;针对红酒、棕色塑胶微粒等荧光背景较强的样品,需结合近红外拉曼光谱和差分拉曼光谱对样品进行定性分析。研究表明：通过多波长消荧光拉曼光谱检测系统的研制,在常规单波长拉曼光谱技术的基础上,将两种抑制荧光干扰技术有机结合,有效扩充了应用领域及样品检测范围。     

Two‐dimensional standoff Raman measurements of distant samples

A scanning standoff Raman spectroscopy system has been developed to measure the molecular species of distant samples in two dimensions. Computer software is used to control the scanner pan and tilt angles, and Raman measurements are collected of the distant sample area in an x–y grid pattern. The Raman spectra at each grid point are measured and processed to obtain an image of the distant surface composition. The ability to provide interpolated images of distant molecular species is illustrated. Copyright © 2011 John Wiley & Sons, Ltd.     

拉曼光谱技术的应用及研究进展

本文简述了拉曼光谱产生的机理以及与红外光谱的区别,讨论了拉曼光谱在聚合物、生物分子、蛋白质和无机物等方面研究及应用,介绍了傅立叶变换拉曼、共焦显微拉曼、表面增强激光拉曼、固体光声拉曼光谱的原理及其应用以及拉曼光谱和其他检测手段的联用技术。     

复合输出镜（Nd,Ce）：YAG拉曼频移激光器研究

报道了由部分反射凹面镜和辅助平面镜构成的复合输出镜高压ＣＨ４气体（Ｎｄ，Ｃｅ）：ＹＡＧ拉曼频移激光器的理论和实验研究结果，在１０Ｊ的输入下，获得１２ｍＪ的拉曼激光输出，并计算的基频场基模光束参数。     

拉曼光谱技术在爆炸物检测中的应用

随着恐怖活动的蔓延,对爆炸物的检测和溯源变得越来越重要。拉曼光谱能够提供化合物的指纹图谱,是对物质定性分析的有力工具,具有无损、快速、准确度高等优点,近年来在爆炸物检测领域被广泛应用。本文介绍了共聚焦显微拉曼光谱、空间偏移拉曼光谱、表面增强拉曼光谱等拉曼光谱技术在爆炸物检测方面的应用及最新研究进展。     

A novel Raman optical activity instrument operating in the deep ultraviolet spectral region

Raman optical activity (ROA) has been exclusively observed in the visible (VIS) and near‐infrared (NIR) spectral regions to date. During the last few years, we have designed, constructed and tested the first ROA instrument, operating in the deep‐ultraviolet (DUV) spectral region employing 244‐nm excitation. This novel DUV ROA instrument is based on a backscattering geometry and incident circular polarization modulation (ICP); it makes use of a fast DUV imaging lens‐based spectrograph and specially designed DUV grade polarization optics. The performance of this instrument has been evaluated by analysing measured non‐resonant DUV ROA spectra of non‐absorbing enantiomeric liquid samples and by comparing these with corresponding ROA spectra recorded in the visible spectral region. Copyright © 2015 John Wiley & Sons, Ltd.     

高压下NaCl水溶液的Raman光谱不连续性的证据

在温度21℃和压力50～1 100 MPa范围内利用碳化硅压腔进行了10%的NaCl水溶液的Raman光谱的原位测量和研究.研究发现:溶液的Raman拟合谱峰在50～300 MPa压力范围内,随着压力的增加向低波数方向移动,在约300 MPa时达到最小值;在300～800 MPa压力范围内,压力的升高则导致谱峰向高波数方向移动,在约800 MPa时达到最大值;随着压力的进一步升高(＞800 MPa),谱峰又向低波数方向移动.类似地,拟合谱峰的峰面积比值和半高宽在压力约300和800 MPa时也发现了不连续现象.这表明高压下NaCl水溶液的内部结构足不连续的,溶液中的氧键(O-H…CL-)发生了相应的变化,意味着溶液中出现了结构的重新排列,产生了较为复杂的结构构型.     

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.     

Raman Scattering Intensities of the NO2 Symmetric Stretching Vibration Band of Some Aromatic Nitrocompounds (II)

The Raman scattering intensities of the NO₂ symmetric stretching vibration band were investigated experimentally for some para and meta substituted nitrobenzenes. The excitation profiles obtained with the six excitation wavelengths from 457.9 to 514.5 nm were presented. The results were examined in terms of the Albrecht-Hutley's theory, and the electronic states involved in the preresonance Raman intensity enhancement were suggested.     

碳纳米管拉曼光谱研究新进展

本文介绍碳纳米管拉曼光谱研究的最新进展。重点介绍金属性和半导体性碳纳米管的共振拉曼效应、表面增强拉曼效应和偏振拉曼效应。同时也介绍了碳纳米管的温度效应、压力效应和杨氏模量的拉曼光谱研究