钽酸锂晶体的喇曼光谱及其方向色散的测定

为了测定钽酸锂铁电晶体异常声子的方向色散,我们找到一种较为满意的直角散射几何配置,制备了十个不同取向的样品,并为消除内反射光引起的附加散射,在样品表面上镀了增透膜,获得了波夫与光轴成不同夹角时的一系列寻常声子和异常声子的喇曼光谱.对这些喇曼光谱进行了识别,认定了四个A_1光学声子和九个E光学声子,确定了十三个异常声子方向色散支.由于全部异常声子的散射峰能始终一起出现在同一喇曼光谱中,使得异常声子方向色散的确定一目了然.最后用单轴晶体异常声子方向色散公式计算了异常声子的方向色散曲线,实验与理论计算相当符合.     

极性倍频晶体中的相干喇曼混频

本文建立了极性倍频晶体中极化声子相干喇曼混频的耦合波方程,其中考虑了超喇曼极化率β_R.该方程在小信号、声子近似以及喇曼驱动的参量近似下求解.结果表明:在高强度泵浦光受激喇曼散射的相干驱动下,极性倍频晶体可以在泵浦光倍频附近产生极化声子的相干喇曼光束.这种光束可以通过不同的相干喇曼混频过程,由倍频光直接转换,或由基波光直接转换,还可以由倍频光与基波光共同转换而成.这三种转换过程具有各自不同的相位失配因子.在一定条件下,后两种过程可以同时进行.在LiIO_3晶体中证实了上述的结论.实验中泵浦光强度约3.0×10~9W/cm~2.     

光声方法研究表面等离子激元衰减

本文用衰减全反射(ATR)和光声(PA)方法研究表而等离子激元(surface plasmons)的衰减,分别对Ag-空气界面和CaF_2-Ag-空气界面进行衰减全反射谱和光声光谱测定.测量结果确定两种衰减方式,辐射和无辐射定量结果,并且发现表面粗糙度对衰减方式有影响.     

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.     

InGaN薄膜的紫外共振喇曼散射

利用325nm紫外光激发,对不同组分的In_xGa_1-xN薄膜的喇曼散射谱进行了研究.在光子能量大于带隙的情况下,观察到显著增强的二阶A₁(LO)声子散射峰.二阶LO声子峰都从一阶LO声子的二倍处向高能方向移动,移动量随样品In组分的增加而增大,认为是带内Frhlich相互作用决定的多共振效应引起的.分析了一阶LO声子散射频率和峰型与In组分的关系.在喇曼谱中观察到样品存在相分离现象,并与X射线衍射的实验结果进行 关键词： xGa_1-xN合金')" href="#">In_xGa_1-xN合金 紫外共振喇曼散射 二阶声子 相分离     

关于顺式聚乙炔共振喇曼谱的理论解释

本文建议以双极化子微观模型,根据多声子晶格弛豫理论解释顺式聚乙炔的喇曼谱。在准一维哈密顿量中考虑了电子与不同声子模的耦合,其耦合常数由红外及喇曼实验数据确定。理论计算结果与实验数据进行了比较和讨论。文中采用的方法可以推广到类似的系统 关键词：     

Ag涂层内凹弧形针尖增强喇曼散射效应仿真研究

设计了一种表面镀有Ag涂层且具有内凹弧度的圆锥形钨(W)针尖,运用时域有限差分法建立了针尖-球形样品结构的针尖增强喇曼散射模型,研究了针尖增强效应及参数优化配置.采用波长632.8nm光源斜入射激励方式,对模型的针尖增强喇曼散射效应进行电磁场仿真计算,获得了模型在不同光源入射角度、样品粒径、针尖-样品间距下的增强电场强度和针尖增强喇曼散射增强因子.研究结果表明:当光源入射角为72°、样品粒径约为140nm、针尖-样品间距达到2nm时可产生最大的增强因子,达到104量级.该结果为制备高增强效率的探针针尖,及其在高空间分辨率和高检测灵敏度喇曼光谱仪中的实用化提供了参考依据.     

三原子分子的喇曼散射

利用U(5)群链描述三原子分子振转谱的对称性质,并用群论方法计算了CO_2分子喇曼散射的跃迁矩阵元,给出了它的振动与转动喇曼散射截面.结果与实验较好地符合.     

单脉冲喇曼散射技术测量高压燃烧场组分浓度

介绍了自发喇曼散射技术的基本原理、实验方法及对高压燃烧场的测量结果。利用Nd:YAG激光的三倍频输出激发振动喇曼散射,在单脉冲条件下测量了高压模拟燃烧室内不同化学配比条件下以氢气-空气预混燃烧场为主要组分(N2,O2,H2O,H2等)的喇曼光谱,获得了主要组分浓度随燃烧时间、燃烧场压力的变化规律。实验中利用偏振技术有效地提高了信噪比。通过优化激光光束形状及光路设计避免了等离子体光谱对喇曼信号的干扰。     

Ag（110）表面声子谱的分析型EAM模型计算

应用晶格动力学，结合分析型EAM模型，计算了Ag(110)表面声子频率和振动极化方向，通过比较弛豫与未弛豫表面的计算结果，发现弛豫后的结果与He原子散射实验数据符合得很好，表面振动的极化局域特征符合表面的二维对称性，沿方向的S2和S3表面模也和实验结果—致. 关键词： 表面声子谱 弛豫 EAM 极化     

Angularly resolved coherent Raman spectroscopy (ARCS) in gases

We report here the development of a Coherent Anti-Stokes Raman Scattering (CARS) configuration which takes advantage of the phasematching criterion to produce simultaneous spatially-separated signals from different constituents within a gas. In particular, we have show that separate CARS beams from nitrogen monoxide may be simultaneously observed from a single sample volume.     

金属微结构纳米线中等离激元传播和分光特性

本文从理论和实验两方面探讨了具有微结构的金属纳米线系统中表面等离激元传播规律和分光特性. 我们由麦克斯韦方程组出发, 利用严格耦合波近似和有限元差分等方法首先从理论上给出了金属纳米线系统中等离激元的色散关系和能带特征, 然后基于微结构的银纳米线及其等离激元能带结构, 设计并制备出等离激元分光原型器件, 实验展示其将不同频率的光在微小空间分离的特性. 该研究结果是我们前期相关工作的延续和补充, 可应用于构造多功能集成的光子芯片和新型亚波长光电材料和器件.     

Multichannel Raman spectroscopy of unroughened noble metal and non-noble metal films and tunnel junctions

We demonstrate that multichannel optical detectors provide the capability of observing Raman Scattering from molecular monolayers in solid-air and solid-solid interfaces in the absence of the conditions considered essential for surface enhanced Raman scattering. We present spectra of adsorbates on smooth Ag films, air-oxidized smooth Al films and Al gratings. Finally, we demonstrate a new configuration for surface enhanced Raman scattering which need not involve noble metals. Raman scattering from a doped Al/AlOx/Sn tunnel junction provides a specific example of such a configuration.     

The effect of the nonparabolicity of the free carriers dispersion law on the propagation of surface polaritons in a semiconductor-metal structure

The results of a study on the influence of the nonparabolicity of the free carriers dispersion law on the propagation of surface polaritons (SPs) located near the interface between an n-type semiconductor and a metal arc reported. The semiconductor plasma is assumed to be warm and nonisothermal. The nonparabolicity of the electron dispersion law has two effects. The first one is associated with nonlinear self-interaction of the SPs. The nonlinear dispersion equation and the nonlinear Schrodinger equation for the amplitude of the SP envelope are obtained. The nonlinear evolution of the SP is studied on the base of the above mentioned equations. The second effect results in third harmonics generation. Analysis shows that these third harmonics may appear as a pure surface polariton, a pseudosurface polariton, or a superposition of a volume wave and a SP depending on the wave frequency, electron density and lattice dielectric constant.     

应用于低折射率样品检测的SERS活性液芯光纤

用纳米组装方法在空心光纤内壁修饰SERS活性基底构成内壁具有表面增强拉曼光谱活性层的液芯光纤。激发光由光纤壁横截面入射,并在光纤壁中传播。由于光纤壁的折射率大于检测样品溶液的折射率,使得激发光在光纤壁中发生全反射,并在消逝场下穿透修饰层,激发样品拉曼散射。本方法融合了表面增强拉曼光谱技术与液芯光纤技术的优势,可成为应用于低折射样品溶液体系检测的又一手段。     

Near-field thermal emission from metamaterials

A closed form expression for the local density of electromagnetic states (LDOS) due to a thermally emitting metamaterial bulk is derived from Maxwell's equations combined with fluctuational electrodynamics. The final form is the same as that for nonmagnetic materials, where the influence of the magnetic permeability is embedded in the Fresnel reflection coefficients. Spectral distributions of LDOS near metallic- and dielectric-based metamaterials are investigated. Results reveal that LDOS profiles are dominated by surface polaritons (SPs) in both TE and TM polarization states. A detailed discussion is provided on the necessary conditions for exciting TM- and TE-polarized SPs via a dispersion relation analysis that accounts for losses. Beyond the conventional conditions for excitation of SPs, the lossy dispersion relation analysis demonstrates mathematically that SPs exist when the imaginary parts of the permittivity or permeability, as well as n′n″, are close to zero, where n′ and n″ are the real and imaginary parts of the refractive index, respectively. An asymptotic expression for the extreme near field LDOS is derived, showing a Δ^?3 power law relationship, as for nonmagnetic media, between LDOS and distance from the emitting bulk Δ. Results obtained from this study will assist in assessing material properties of arbitrarily electromagnetic materials in applications related to energy harvesting.     

Surface plasma waves in the noble metals

The dispersoon curves for surface plasma waves (SPW) in Ag have been determined from calculated reflectivity minima as exhibited by attenuated total reflection (ATR spectra) for the prism-metal-air (PMA) configuration and from the direct calculation of the dispersion relation for the same configuration. Comparison is made with published results. The dispersion curves for Au and Cu have been determined for the same configuration from calculated ATR spectra and verified experimentally. Comparison is made with the direct calculation of the dispersion relation. The direct calculation yields two types of modes; namely the surface or Brewster mode and the virtual mode. Both modes are discussed. The marked effect of small electronic damping as exhibited by Ag and moderate electronic damping as exhibited by Au and Cu upon the PMA dispersion curves from ATR spectra is examined. Finally the direct calculation of the dielectric shift (perturbing effect of the prism-metal surface upon the active metal-air surface dispersion curve) is presented for the three metals as a function of film thickness and photon energy.     

受激拉曼散射对非线性介质波导的时空不稳定性影响

基于非线性包络方程我们研究了平面非线性介质波导中的时空不稳定性,得到了有拉曼散射效应情形下不稳定性调制的增益谱的表达式.结果表明在正常和反常两种群速度色散情形下,拉曼散射效应都会导致出现新的不稳定性区域,并且使原有的每一个谱分量的增益上升从而使谱的范围扩大.并通过分析反常色散情况下四种不同函数分布的非线性色散介质系数对不稳定性增益谱的影响,得到呈双曲函数分布的非线性色散介质最为理想.     

Surface polariton dispersion measurement by Raman scattering excited in total reflection condition

We report the first measurement of phonon surface polariton (s.p.) dispersion by a non-forward Raman scattering geometry. The Raman scattering from surface modes was excited by the evanescent electromagnetic wave produced by total reflection at the interface between two transparent media. This Raman Scattering excited in condition of Total Reflection, RSTR, has been applied to the NaClO₃-sapphire interface for studying the surface polariton dispersion in the gap between the TO frequency at 966 cm^-1 and the LO frequency at 983 cm^-1 of sodium chlorate. Comparison is made between the experimental and theoretical dispersion curves.     

Survival of molecular information under surfaced‐enhanced resonance Raman (SERRS) conditions

In the present paper, we discuss the molecular information that can be derived from surface‐enhanced resonance Raman Scattering (SERRS) experiments performed with different excitation wavenumbers, which are close to resonance with an excited electronic state of the molecule [surface‐enhanced Raman dispersion spectroscopy (SERADIS)]. We specifically consider the situation, where a molecule is physisorbed to a site characterized by a local electric field with a direction independent of the direction of the external, exciting field. The molecular information available in this experimental situation is compared with the information available in a corresponding Raman dispersion spectroscopy (RADIS) experiment performed on a free molecule or a molecule physisorbed to a site, where the local field is isotropic. The consequences for resonance Raman scattering (RRS) and RADIS, when the molecule is adsorbed in the highly anisotropic hot spot (HS), are discussed; here it is shown that only the molecular information originating from the symmetric part of the scattering tensor can survive in SERRS and in SERADIS. Besides, it is shown that the depolarization ratio can no longer be used to discriminate between totally and non‐totally symmetric modes in the polarized surface‐enhanced Raman scattering (SERS) spectra. These results have implications for the resonance Raman spectra, but even more important for the application of the resonance Raman effect in the investigation of excited vibronic molecular states, in general, and in the investigation of electronic states in larger bio‐molecules, such as the various metallo‐porphyrins. Copyright © 2009 John Wiley & Sons, Ltd.