光纤背向激光自发喇曼散射的温度效应研究

从理论和实验上研究了光纤背向激光自发喇曼散射的温度效应.光纤背向激光自发反斯托克斯喇曼散射、斯托克斯喇曼散射光的相对强度正比于光纤分子上、下能级粒子数的布居,依赖于温度.由于实际系统中,作为分光用的干涉滤光片不可能完全隔离背向瑞利散射光,因此,实际系统温度曲线比理论曲线低,本文给出了理论修正公式,提出了附加修正项,它与隔离度和波长有关.     

大口径DKDP晶体受激拉曼散射增益系数的测量（英）

大口径KDP/DKDP晶体在强紫外光辐照下产生横向受激拉曼散射效应（TSRS）, 受激放大的拉曼散射光将导致激光能量损失甚至激光损伤, 测量DKDP晶体TSRS增益系数对设置激光装置的运行区间以确保晶体的安全使用非常重要。采用高精度光谱仪探测大口径DKDP晶体（氘含量65%）在351 nm激光辐照下的横向拉曼散射信号, 得到了拉曼散射光的增长曲线, 拟合得到的拉曼增益系数为0.109 cm/GW。同时, 实验结果表明晶体体损伤不影响TSRS增长行为, 表明晶体体损伤对拉曼增益系数测量结果的影响可以忽略。     

Surface-enhanced raman scattering and nonlinear optics applied to electrochemistry

The most recently developed diagnostic technique in metal-electrolyte and metal-gas interfaces adapts spontaneous Raman scattering and nonlinear optical generation, techniques normally applied to bulk media, to surface science investigation. For certain metallic surfaces, an enormous increase exists in the Raman (as much as 10⁶ to 10⁸ times) and nonlinear optical signals resulting from submonolayer coverage of molecular adsorbates at the interface. Spontaneous Raman scattering and nonlinear optical scattering are well developed in both theory and practice for the analysis of molecular structure and concentration in bulk media. Instrumentation to generate and detect these inelastically scattered signals is readily available and is adequate for adaption to surface science. However, the mechanism (or mechanisms) giving rise to such a large enhancement at the interfaces is still being actively researched and remains controversial. Theoretical and experimental investigations related to the underlying physics of this enhancement and the application of such surface enhancement as a vibrational probe for adsorbates on the metal surface have been labeled “surface-enhanced Raman scattering” (SERS) and “surface-enhanced nonlinear optics”. Soon after the recognition that molecules adsorbed onto metal electrodes under certain conditions exhibit an anomalously large Raman scattering efficiency,^1–3 it became evident that such a phenomenon makes possible an in situ diagnostic probe for detailed and unique vibrational signatures of adsorbates in the ambient phase (electrolyte and atmospheric gas surroundings). Optical spectroscopy in the visible range has a much higher energy resolution (e.g., 0. I cm-I) than is presently available in electron energy loss spectroscopy (EELS), as well as the capability to measure much lower frequency modes (e.g., as low as 5 cm^?1) than is possible in infrared spectroscopy. Perhaps the most significant attribute of SERS and surface-enhanced nonlinear optical scattering is that the surrounding media in front of the interface (e.g., several meters of gas and several centimeters of liquid) do not introduce optical loss or overwhelmingly large signals. The recognition that SERS is capable of performing vibrational spectroscopy with this resolution, frequency range, and in such dense surroundings has therefore brought an explosion of activity to the field since 1977.     

Surface enhanced Raman scattering by CdS quantum dots

Surface enhanced Raman scattering is studied in nanostructures with CdS quantum dots formed using the Langmuir-Blodgett technology. Features due to quantum dot longitudinal optical phonons are observed in the Raman spectra of both free CdS quantum dots and such dots distributed in an organic matrix. The surface enhanced Raman scattering by nanostructures with CdS quantum dots covered by an Ag cluster film is observed experimentally. Applying Ag clusters onto the nanostructure surfaces results in a sharp (40-fold) increase in the intensity of Raman scattering by optical phonons in the quantum dots. It is shown that the dependence of surface enhanced Raman scattering on the excitation energy is resonant with a maximum at the energy corresponding to the maximum absorption coefficient of Ag clusters.     

All-optical switching based on inverse Raman scattering in liquid-core optical fibers

We report on a new platform for all-optical switching based on inverse Raman scattering in liquids. Narrowband switching, which could be suitable for wavelength-division-multiplexed applications, is demonstrated using integrated liquid-core optical fiber infiltrated with both neat liquids (CCl(4) and CS(2)) as well as an organic chromophore (β-carotene) dissolved in CCl(4). Compared to standard glass optical fibers, these liquids have much larger Raman loss coefficients, which help reduce the pump power by at least an order of magnitude. Further improvements can be expected with the development of highly soluble organic compounds possessing large Raman cross sections.     

Spectral power handling capability caused by stimulated Raman scattering effect in silica optical fibers

Spectral characteristics of the stimulated Raman scattering (SRS) in silica fibers was studied for the purpose of obtaining higher power transmission capability in single-mode silica optical fibers. When the input power exceeds a critical input power, which depends on the wavelength, nonlinear transmission loss caused by SRS gives rise to excess loss and signal waveform distortion. The SRS effect is reduced under the condition of sufficiently large spectral loss at the first Stokes wavelength.     

Determination of the LO phonon energy by using electronic and optical methods in AlGaN/GaN

The longitudinal optical (LO) phonon energy in AlGaN/GaN heterostructures is determined from temperature-dependent Hall effect measurements and also from Infrared (IR) spectroscopy and Raman spectroscopy. The Hall effect measurements on AlGaN/GaN heterostructures grown by MOCVD have been carried out as a function of temperature in the range 1.8-275 K at a fixed magnetic field. The IR and Raman spectroscopy measurements have been carried out at room temperature. The experimental data for the temperature dependence of the Hall mobility were compared with the calculated electron mobility. In the calculations of electron mobility, polar optical phonon scattering, ionized impurity scattering, background impurity scattering, interface roughness, piezoelectric scattering, acoustic phonon scattering and dislocation scattering were taken into account at all temperatures. The result is that at low temperatures interface roughness scattering is the dominant scattering mechanism and at high temperatures polar optical phonon scattering is dominant.     

拉曼散射在有线电视传输中的应用

本文叙述了拉曼散射的原理,结合拉曼散射理论,讨论了光纤拉曼放大器的优缺点,并根据现阶段有线电视的传输方式和将来的发展趋势,论证了光纤拉曼放大器用于CATV的重要性和不可或缺性.     

光纤中双孤子相互作用的等价粒子理论

本文给出了含有一般扰动的非线性薛定锷（Ｓｃｈｒｏｄｉｎｇｅｒ）方程的孤子等价粒子理论，它使人们对孤子的粒子性质有了更深的了解，同时给出了光纤中双孤子相互作用的等价粒子分析，得到了与基于逆散射及微扰变分法完全一致的结果，这一方法可用于多孤子相互作用的解析分析，并能给出这一过程的直观物理图象．     

Monitoring stimulated Raman scattering with photoacoustic detection

A capability of high-frequency ultrasound detection to monitor the process of energy deposition into a molecular system via Raman excitation is experimentally demonstrated. It is shown that the generated ultrasound signal is directly proportional to the optical signal generated in stimulated Raman scattering. Ultrasound detection provides a simple way to discriminate against laser-induced breakdown and allows for the quantification of the stimulated Raman scattering process where direct optical detection is not available. Additionally, it can be used for stimulated Raman imaging in deep tissue, provided that the generated photoacoustic signal is sufficiently strong.     

α-石英晶体中旋光性对Raman散射的影响

讨论了旋光性对Raman散射的影响。在α-石英晶体中获得了消除旋光影响的纯Raman谱,在此基础上,讨论了α-石英晶体(单轴晶体)的Raman谱中,x轴和y轴的非等价性问题,以及与这种非等价性相应的振动模的对称性。 关键词：     

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。     

Resonant Raman detection of macular pigment levels in the living human retina

We have used resonant Raman scattering as a novel, noninvasive in vivo optical technique to measure the concentration of macular carotenoid pigments in the living human retina. Using a backscattering geometry and resonant molecular excitation in the visible, we measure the Raman peaks that originate from the single- and double-bond stretch vibrations of the p -conjugated molecule's carbon backbone. The Raman signals scale linearly with carotenoid content, whereas the required laser excitation is well under safety limits for macular exposure. The Raman technique is objective and quantitative and may lead to a new method for rapid screening of carotenoid pigment levels in large human populations that are at risk for vision loss from age-related macular degeneration, the leading cause of blindness of the elderly in the United States.     

基于累加平均的分布式光纤拉曼测温系统

分布式光纤拉曼温度传感(DTS)系统是一套基于光纤中的拉曼散射效应来实现分布式温度监控的系统,利用光纤中拉曼散射光的强度与光纤的温度状态有关的原理对温度进行实时监测。设计了一套9 km的光纤拉曼测温系统,利用数据采集卡对斯托克斯和反斯托克斯光进行采集,在电脑端对温度进行累加平均处理,将微弱的信号从系统的噪声中提取出来,提高其信噪比。在累加平均16 000次的情况下测温精度达到了±2℃。     

Raman scattering using vortex light

We re-examine the theory of Raman scattering in cubic crystals. The unconventional vector potential of vortex light leads to new selection rules. We show that in this novel optical process, (a) silent phonon modes become active and (b) scattering tensors change for ordinary Raman active phonon modes. Calculation based on a simplified model shows that the vortex Raman scattering intensity can be comparable with that of ordinary Raman process.     

Surface-enhanced Raman spectroscopy of semiconductor nanostructures

We review our recent results concerning surface-enhanced Raman scattering (SERS) by confined optical and surface optical phonons in semiconductor nanostructures including CdS, CuS, GaN, and ZnO nanocrystals, GaN and ZnO nanorods, and AlN nanowires. Enhancement of Raman scattering by confined optical phonons as well as appearance of new Raman modes with the frequencies different from those in ZnO bulk attributed to surface optical modes is observed in a series of nanostructures having different morphology located in the vicinity of metal nanoclusters (Ag, Au, and Pt). Assignment of surface optical modes is based on calculations performed in the frame of the dielectric continuum model. It is established that SERS by phonons has a resonant character. A maximal enhancement by optical phonons as high as 730 is achieved for CdS nanocrystals in double resonant conditions at the coincidence of laser energy with that of electronic transitions in semiconductor nanocrystals and localized surface plasmon resonance in metal nanoclusters. Even a higher enhancement is observed for SERS by surface optical modes in ZnO nanocrystals (above 10⁴). Surface enhanced Raman scattering is used for studying phonon spectrum in nanocrystal ensembles with an ultra-low areal density on metal plasmonic nanostructures.     

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.     

Thermal loss mechanism in the generation of multifrequency laser emission via stimulated Raman scattering and four-wave Raman mixing studied by photothermal refraction spectroscopy

The heat produced in conjunction with the processes of stimulated Raman scattering and four-wave Raman mixing in hydrogen was measured by photothermal refraction spectroscopy. Many vibrational, rotational, and vibrationally shifted rotational Raman lines are exclusively/simultaneously generated by changing the polarization of the laser beam and the hydrogen pressure. Thermal loss occurs predominantly from vibrational Raman scattering, which can be ascribed to a large Raman shift frequency of 4155 cm^-1 for the vibrational transition. In contrast to stimulated Raman scattering, little or no thermal loss is observable during the process of four-wave Raman mixing. Received: 12 April 1999 / Revised version: 12 July 1999 / Published online: 20 October 1999     

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：     

Background-free coherent Raman spectroscopy by detecting the spectral phase of molecular vibrations

We propose and demonstrate a new approach to subtracting high nonresonant background in coherent anti-Stokes Raman scattering spectroscopy. The method is based on the retrieval of the spectral phase of molecular vibrations using the technique of frequency-resolved optical gating of Raman scattering. In the presence of high nonresonant background the retrieved phase corresponds directly to the background-free spectrum of the coherent Raman response.