苯C—H伸缩振动弱增益模式的受激拉曼散射

对苯的长拉曼振动模式C—H(3060 cm^-1线)伸缩振动的一阶受激拉曼散射进行了实验研究.利用在苯溶液中加入甲苯溶液,在液芯光纤内实现了苯的全对称C—H伸缩振动3060 cm^-1线的受激拉曼散射.利用等离子体解释了这一增强机理. 关键词： 液芯光纤 受激拉曼散射 等离子体     

溶剂折射率对β-胡萝卜素拉曼散射截面的影响

以环己烷的1444 cm^-1拉曼线为内标,采用5145 nm激发光分别测量了β-胡萝卜素的C=C双键（1520 cm^-1）和C—C单键（1155 cm^-1）振动模式下在不同折射率溶剂中的拉曼散射截面,结果表明随溶剂的折射率增加β-胡萝卜素在两种振动模式下拉曼散射截面都增加.利用色散力和共振拉曼理论解释了在不同折射率溶剂中β-胡萝卜素散射截面的差异. 关键词： 拉曼散射截面 β-胡萝卜素 色散力 共振拉曼     

采用圆偏振啁啾飞秒激光脉冲操控CS2分子的相干拉曼散射过程

采用两束圆偏振啁啾飞秒激光脉冲,非共线相干激发三原子分子CS₂液体. 在相位匹配的方向上,探测到由CS₂频率为397 cm^-1的振动模式产生的强度对称分布的相干反斯托克斯拉曼散射(CARS)信号和相干斯托克斯拉曼散射(CSRS)信号. 当调整两束激发光的圆偏振状态时,CARS,CSRS信号的强度、偏振、波长均发生规律性的改变:CARS,CSRS信号的强度分布反映了CS₂ 在不同极化状态下的受激拉曼散射截面大小;信号光的 关键词： 啁啾脉冲 相干反斯托克斯拉曼散射(CARS) 相干斯托克斯拉曼散射(CSRS) 2')" href="#">CS₂     

不同波长激光激发下C6H12受激拉曼散射模式竞争

发现不同波长激光激发下C₆H₁₂的受激拉曼散射模式竞争现象. 在不同波长的激光激发下，不同拉曼模式的Stokes光占优势. 短波长(404，532nm)激光激发时小频移模式ω₁(802cm^-1)为弱增益模式，大频移模式ω₂(2852—3038cm^-1)为强增益模， 主要产生ω₂模式的Stokes光. 长波长(80 关键词： 模式竞争 6H₁₂')" href="#">C₆H₁₂ 受激拉曼散射     

Bi2ZnOB2O6单晶偏振拉曼光谱

本文通过分析不同几何配置下的偏振拉曼光谱对非线性光学晶体的晶格振动模式进行了研究. 首先根据因子群分析,将晶体的振动模按晶体对称群的不可约表示进行分类,其次测量了晶体在10–1600 cm^-1范围内,不同几何配置下的偏振拉曼光谱,并在此基础上指认了晶体的晶格振动模式. 300 cm^-1以下的振动峰,归结为晶体的外振动,来自[BiO₆],[ZnO₄],[BO₄]和[BO₃]原子基团的平动和转动;300cm^-1以上为晶体的内振动,主要与Bi-O,和Zn-O键振动有关. 晶体拉曼光谱中最高振动频率达到1407 cm^-1,被指认为[BO₃]三角形中B-O键的伸缩振动,体现了[BO₃]基团中高的电子非局域化程度. 关键词： 2ZnOB₂O₆单晶')" href="#">Bi₂ZnOB₂O₆单晶 偏振拉曼光谱 振动模式     

苏氨酸的太赫兹及拉曼光谱研究

采用太赫兹时域光谱和拉曼光谱法对L-苏氨酸多晶粉末进行测试研究,获得了样品在0.2—2.8 THz（6.7—93.2 cm^-1）波段的特征吸收和10—4000 cm^－1波段的拉曼散射谱;分别在6.7—93.2 cm^－1和400—4000 cm^－1两个波段进行了吸收光谱与拉曼散射光谱的对比,根据晶胞分子所属的空间群,对隶属于分子的极性和非极性振动模式（A, B₁, 关键词： 太赫兹光谱 拉曼散射 氨基酸     

自受激拉曼晶体Nd3+:SrMoO4的光谱性质研究

通过拉曼散射光谱，吸收光谱，荧光发射寿命和808 nm LD激发下的红外荧光光谱的实验测量，系统研究了Nd³⁺:SrMoO₄晶体的自受激拉曼光谱性质.分析指认了拉曼散射光谱中各拉曼峰所对应的晶格振动模式，得出了其SRS活性最强的声子频率约为898 cm^-1，对应于(MoO^2-₄)离子团的完全对称光学伸缩振动A_g模；通过J-O理论对晶体的吸收谱进行了全面的光谱参数计算，得出⁴F_3/2→⁴I_11/2跃迁的积分发射截面达0.57×10^-18 cm²，自发辐射概率为141.06 s^-1；同时，实验测得该跃迁的荧光发射寿命约为0.2 ms.最后，结合808 nm LD激发下的红外波段荧光光谱，论证了SrMoO₄晶体中Nd³⁺离子1068 nm发射通过拉曼频移获得1180 nm一级斯托克斯激光发射的可能性，为Nd³⁺:SrMoO₄晶体的自受激拉曼激光器研究提供了理论依据. 关键词： 3+离子')" href="#">d³⁺离子 4 晶体')" href="#">SrMoO₄ 晶体 自受激拉曼散射     

BaBPO5晶体晶格振动光谱研究与第一性原理计算

通过偏振拉曼光谱和第一性原理计算对非线性光学晶体BaBPO₅的 晶格振动模式进行了研究. 实验得到了不同几何配置下、在100–1600 cm^-1范围内的晶体偏振拉曼光 谱与傅里叶变换红外吸收谱, 结合因子群分析方法研究了晶体的外振动与内振动模式特征. 分析表明拉曼振动主要来自于PO₄四面体和BO₄四面体的振动, 且PO₄基团振动具有较强的拉曼与红外活性. 此外,根据第一性原理对晶体拉曼振动进行了数值模拟, 进一步明确了拉曼峰与晶体中原子振动的对应关系, 计算表明拉曼光谱中位于672 cm^-1峰位来自晶体中B–O–P键的伸缩振动, 这是晶体中PO₄四面体和BO₄四面体共顶点连接的特征结构在光谱中的体现.     

NH4H2PO4和ND4D2PO4晶体微结构的拉曼光谱研究

本文利用偏振拉曼光谱和第一性原理, 对磷酸二氢铵(NH₄H₂PO₄, ADP)和不同氘含量磷酸二氢铵DADP晶体的晶格振动模式进行了研究. 实验测得了不同几何配置、200–4000 cm^-1范围的偏振拉曼光谱, 分析在不同氘含量条件下921 cm^-1和3000 cm^-1附近拉曼峰的变化. 在ADP晶体中, 基于基本结构单元NH₄⁺ 和H₂PO₄^-基团的振动模, 用第一性原理进行了数值模拟, 进一步明确拉曼峰与晶体中原子振动的对应关系; 通过洛伦兹拟合不同氘含量DADP晶体的拉曼光谱中2000–2600 cm^-1处各峰的变化讨论了DADP 晶体的氘化过程, 结果表明氘化顺序是先NH₄⁺ 基团后H₂PO₄^-基团, 研究结果为今后此类材料的生长和性能优化奠定了基础.     

液芯光纤中溶液吸收和荧光的性质对CS2受激拉曼散射阈值的影响

利用液芯光纤技术研究了不同浓度的β-Carotene的CS₂溶液的吸收与荧光的特性对CS₂的一、二阶Stokes谱线阈值的影响.实验发现随溶液浓度(10^-8—10^-6 mol/L)增加，CS₂的一阶Stokes谱线的激发阈值相对变高；并且与纯CS₂芯液的受激拉曼散射相比较，在低抽运能量激发下，就观察到CS₂的二阶Stokes谱线.这主要是由于在CS₂的受激拉曼谱线产生的过程中，β-Carotene的CS₂溶液的吸收和荧光共同影响了CS₂的一、二阶Stokes谱线的阈值.我们进行了理论上的拟合与分析，其结果与实验符合很好. 关键词： 2受激拉曼散射阈值')" href="#">CS₂受激拉曼散射阈值 液芯光纤 吸收与荧光     

Enhanced stimulated Raman scattering by intermolecular Fermi resonance

We demonstrate the stimulated Raman scattering (SRS) of a binary solution of toluene and m-xylene at different volume concentrations in liquid-core optical fiber (LCOF). The results show that SRS of three vibration modes of 1002 cm⁻¹,2920 cm⁻¹ and 3058 cm⁻¹ bands are simultaneously generated at some volume concentrations. The 2920 cm⁻¹ band and the 3058 cm⁻¹ band are generated at one time, the SRS thresholds of the first-order Stokes of the 2920 cm⁻¹ and 3058 cm⁻¹ bands are lower compared with the second-order Stokes threshold of the 1002 cm⁻¹ band and the main peak of the 2920 cm⁻¹ and 3058 cm⁻¹ bands changes from the 2920 cm⁻¹ band to the 3058 cm⁻¹ band as the volume concentrations are changed. We assume that these phenomena are attributed to the intermolecular Fermi resonance. Raman scattering cross section (RSCS) theory is used to explain this assumption.     

用激光增益获取弱增益拉曼模式的受激拉曼散射光谱

当酒精的弱增益拉曼模式处于罗丹明640染料分子的激光增益范围时，在由悬垂液滴构成的圆形谐振腔中，观察到乙醇分子C—H伸缩系列模中多个弱增益拉曼模式的受激拉曼散射（SRS）光谱.随着抽运光的增强，迅速增长的强增益拉曼模式的受激辐射抑制了其他弱增益模式的SRS，并导致染料激光的完全淬灭.通过分析圆形腔腔模的光子速率方程和激光染料分子的三能级粒子数速率方程，解释了观察到的实验现象. 关键词： 受激拉曼散射 悬垂液滴 弱拉曼增益模式 激光增益     

Surface enhanced Raman scattering of 2-cyanopyridine adsorbed on silver colloidal particles

Surface-enhanced Raman scattering (SERS) spectra of 2-cyanopyridine (2 CP) adsorbed on silver colloidal particles have been investigated. The prominent SERS bands are observed at 556, 612, 778, 1002, 1060, 1072, 1150 and 1240 cm⁻¹. The absolute enhancement factor of the Raman signals in SERS studies has been estimated to be of the order of 10²–10⁵ for various bands. The 2CP molecules have been ascribed to adsorb on colloidal particles in standing up fashion.     

Beryllium Silicate,Be2SiO4 (phenakite) – a Novel Trigonal SRS‐Active Crystal

In single crystals of the beryllium silicate Be₂SiO₄ with trigonal symmetry , known also as the mineral phenakite, χ⁽³⁾‐nonlinear lasing by stimulated Raman scattering (SRS) is investigated. All observed Stokes and anti‐Stokes lasing components are identified and ascribed to a single SRS‐promoting vibration mode with ω_SRS ≈876 cm⁻¹. With picosecond single‐wavelength pumping at one micrometer the generation of an octave‐spanning Stokes and anti‐Stokes comb is observed.     

Continuous wave stimulated Raman scattering of benzene by fluorescence enhancement in hollow fused silica fiber

We present continuous wave stimulated Raman scattering (SRS) of benzene (C₆H₆) influenced by the fluorescent dye m‐cresol purple in a hollow fused silica fiber (HFSF). Because of the transmission loss of the HFSF filled with C₆H₆, the SRS occurs when the Stokes gain equals the transmission loss, with the loss taken at the Stokes wavelength. The 992 cm⁻¹ stimulated Stokes line has been obtained at the pump wavelength 658 nm, which cannot be obtained at 532 nm because the Stokes wavelength (562 nm) does not locate in the transmission loss. Also, the pump power is 35 mW with m‐cresol purple which is much lower than 800 mW without the dye. The profile of the 992 cm⁻¹ stimulated Stokes is changed, and the weak shoulders of the profile are amplified by fluorescence. These results are expected to be of relevance in applications on the tunable Raman laser at new wavelengths. Copyright © 2011 John Wiley & Sons, Ltd.     

High‐order Stokes and anti‐Stokes Raman generation in monoisotopic CVD 12C‐diamond

We determined, for the first time, the room temperature phonon energy related to the F_2g vibration mode (ω_SRS(12C) ～ 1333.2 cm^–1) in a mono‐crystalline single‐isotope CVD ¹²C‐diamond crystal by means of stimulated Raman scattering (SRS) spectroscopy. Picosecond one‐micron excitation using a Nd³⁺:Y₃Al₅O₁₂‐laser generates a nearly two‐octave spanning SRS frequency comb (～12000 cm^–1) consisting of higher‐order Stokes and anti‐Stokes components. The spacing of the spectral lines was found to differ by Δω_SRS ～ 0.9 cm^–1 from the comb spacing (ω_SRS(natC) ～ 1332.3 cm^–1) when pumping a conventional CVD diamond crystal with a natural composition of the two stable carbon isotopes ¹²C (98.93%) and ¹³C (1.07%). (© 2016 WILEY‐VCH Verlag GmbH &Co. KGaA, Weinheim)     

光纤维中的喇曼混频

我们在656厘米^-1到1343厘米^-1的频率范围研究了光纤维的调谐喇曼混频(RM)效应。在实验中观察到下列现象:相干反斯托克斯喇曼散射(CARS)的大小与逆喇曼吸收(VRA)的大小成反比;RM对受激喇曼散射(SRS)的强度分布有强烈影响。除了观测到相干斯托克斯(CSRS)和CARS辐射,还观测到二级相干斯托克斯(SOCSRS)和相干反斯托克斯(SOCARS)辐射。对实验结果进行了讨论。 关键词：     

Cerussite,PbCO3 – a new Stimulated Raman Scattering (SRS)‐active crystal with high‐order Stokes and anti‐Stokes lasing

Orthorhombic PbCO₃, known as natural crystal cerussite, is presented as a new Stimulated Raman Scattering (SRS)‐active crystal. With picosecond laser pumping high‐order Raman‐induced χ⁽³⁾ generation is observed. All registered Stokes and anti‐Stokes sidebands in the visible and near‐IR are identified and attributed to the SRS‐promoting phonon mode A_1g of the carbonate group, with ω_SRS ≈ 1054 cm⁻¹. The first Stokes steady‐state Raman gain coefficient in the visible spectral range is estimated as well to a value not less than 4.6 cm·GW⁻¹.     

Detection of a new SRS‐promoting phonon mode and cross‐cascaded χ(3)‐nonlinear lasing in single crystals of calcite (trigonal CaCO3)

For calcite (CaCO₃), one of the pioneer crystals in nonlinear optics, new results of stimulated Raman scattering (SRS) spectroscopy are presented. Among them are the discovery of a new SRS‐promoting vibration mode with ω_SRS2 ≈︁ 282 cm^‐1 and its participation, together with the main SRS mode ω_SRS1 ≈︁ 1086.5 cm^‐1, in cross‐cascaded (χ⁽³⁾ ↔ χ⁽³⁾) nonlinear‐lasing generation, as well as the observation of efficient self‐upconversion via cascaded parametric four‐wave processes of one‐micron Stokes and anti‐Stokes χ⁽³⁾‐lasing into the UV‐region of third harmonic generation. The investigations show that calcite is able to generate a χ⁽³⁾‐lasing comb of more than two octaves bandwidth. The article also gives a brief review on the discovery and study of the SRS‐effect in natural crystals (minerals), which have expanded our ability to study the photon‐phonon nonlinear‐laser interactions in crystalline materials. A short summary of information about χ⁽³⁾‐lasing properties of the triangular planar structure units in SRS‐active crystals is included.     

Measurement of the third‐order nonlinear optical susceptibility χ(3) for the 1002‐cm–1 mode of benzenethiol using coherent anti‐Stokes Raman scattering with continuous‐wave diode lasers

The components of the third‐order nonlinear optical susceptibility χ⁽³⁾ for the 1002‐cm^–1 mode of neat benzenethiol have been measured using coherent anti‐Stokes Raman scattering with continuous‐wave diode pump and Stokes lasers at 785.0 and 852.0 nm, respectively. Values of 2.8 ± 0.3 × 10^–12, 2.0 ± 0.2 × 10^–12, and 0.8 ± 0.1 × 10^–12 cm·g^–1·s² were measured for the xxxx, xxyy, and xyyx components of |3χ⁽³⁾|, respectively. We have calculated these quantities using a microscopic model, reproducing the same qualitative trend. The Raman cross‐section σ_RS for the 1002‐cm^–1 mode of neat benzenethiol has been determined to be 3.1 ± 0.6 × 10^–29 cm² per molecule. The polarization of the anti‐Stokes Raman scattering was found to be parallel to that of the pump laser, which implies negligible depolarization. The Raman linewidth (full‐width at half‐maximum) Γ was determined to be 2.4 ± 0.3 cm^–1 using normal Stokes Raman scattering. The measured values of σ_RS and Γ yield a value of 2.1 ± 0.4 × 10^–12 cm·g^–1·s² for the resonant component of 3χ⁽³⁾. A value of 1.9 ± 0.9 × 10^–12 cm·g^–1·s² has been deduced for the nonresonant component of 3χ⁽³⁾. Copyright © 2011 John Wiley & Sons, Ltd.