Simultaneous measurements of global vibrational spectra and dephasing times of molecular vibrational modes by broadband time-resolved coherent anti-Stokes Raman scattering spectrography

In broadband coherent anti-Stokes Raman scattering （CARS） spectroscopy with supercontinuum （SC）, the simultaneously detectable spectral coverage is limited by the spectral continuity and the simultaneity of various spectral components of SC in an enough bandwidth. By numerical simulations, the optimal experimental conditions for improving the SC are obtained. The broadband time-resolved CARS spectrography based on the SC with required temporal and spectral distributions is realised. The global molecular vibrational spectrum with well suppressed nonresonant background noise can be obtained in a single measurement. At the same time, the measurements of dephasing times of various molecular vibrational modes can be conveniently achieved from intensities of a sequence of time-resolved CARS signals. It will be more helpful to provide a complete picture of molecular vibrations, and to exhibit a potential to understand not only both the solvent dynamics and the solute-solvent interactions, but also the mechanisms of chemical reactions in the fields of biology, chemistry and material science.

Selective excitation of molecular mode in a mixture by femtosecond resonance-enhanced coherent anti-Stokes Raman scattering spectroscopy

Femtosecond time-resolved coherent anti-Stokes Raman scattering （CARS） spectroscopy is used to investigate gaseous molecular dynamics. Due to the spectrally broad laser pulses, usually poorly resolved spectra result from this broad spectroscopy. However, it can be demonstrated that by the electronic resonance enhancement optimization control a selective excitation of specific vibrational mode is possible. Using an electronically resonance-enhanced effect, iodine molecule specific CARS spectroscopy can be obtained from a mixture of iodine-air at room temperature and a pressure of 1 atm （corresponding to a saturation iodine vapour as low as about 35 Pa）. The dynamics on either the electronically excited state or the ground state of iodine molecules obtained is consistent with previous studies （vacuum, heated and pure iodine） in the femtoseeond time resolved CARS spectroscopy, showing that an effective method of suppressing the non-resonant CARS background and other interferences is demonstrated.

Selective excitation and suppression of coherent anti-Stokes Raman scattering by shaping femtosecond pulses

Femtosecond coherent anti-Stokes Raman scattering （CARS） suffers from poor selectivity between neighbouring Raman levels due to the large bandwidth of the femtosecond pulses. This paper provides a new method to realize the selective excitation and suppression of femtosecond CARS by manipulating both the probe and pump （or Stokes） spectra. These theoretical results indicate that the CARS signals between neighbouring Raman levels are differentiated from their indistinguishable femtosecond CARS spectra by tailoring the probe spectrum, and then their selective excitation and suppression can be realized by supplementally manipulating the pump （or Stokes） spectrum with the π spectral phase step.

Coherent coupling between vibrational modes of C-H bonds at different positions studied by femtosecond time-resolved coherent anti-Stokes Raman scattering

We performed femtosecond time-resolved coherent anti-Stokes Raman scattering （fs-CARS） measurements on liquid toluene and PVK film. For both samples, we selectively excited the CH stretching vibrational modes and observed the expected quantum beat signals. The frequency of the well-defined beats is in good agreement with the energy difference between the two simultaneously excited modes, which demonstrates that a coherent coupling between the vibrational modes of the C H chemical bonds exists at the different positions of the molecules. The dephasing times of the excited modes are obtained simultaneously.

High-resolution imaging of graphene by tip-enhanced coherent anti-Stokes Raman scattering

Coherent anti-Stokes Raman scattering(CARS)is able to enhance molecular signals by vibrational coherence compared to weak Raman signal.The surface or tip enhancement are successful technologies,which make it possible for Raman to detect single molecule with nanometer resolution.However,due to technical diffculties,tip-enhanced CARS(TECARS)is not as successful as expected.For single molecular detection,high sensitivity and resolution are two main challenges.Here,we reported the first single atom layer TECARS imaging on Graphene with the highest resolution about 20 nm,which has ever been reported.The highest EF_(TECARS/CARS) is about 10^(4),the similar order of magnitude with SECARS(EF of tip is usually smaller than that of substrates).Such resolution and sensitivity is promising for medical,biology and chemical applications in the future.

COHERENT ANTI-STOKES RAMAN SCATTERING MICROSCOPY TO MONITOR DRUG DISSOLUTION IN DIFFERENT ORAL PHARMACEUTICAL TABLETS

Coherent anti-Stokes Raman scattering(CARS)microscopy is used to visualize the release of a model drug(theophylline)from a lipid(tripalmitin)based tablet during dissolution.The effects of transformation and dissolution of the drug are imaged in real time.This study reveals that the manufacturing process causes significant differences in the release process:tablets prepared from powder show formation of theophylline monohydrate on the surface which prevents a controlled drug release,whereas solid lipid extrudates did not show formation of monohydrate.This visualization technique can aid future tablet design.

Wide-Field Vibrational Phase Contrast Imaging Based on Coherent Anti-Stokes Raman Scattering Holography

We propose and implement a wide-field vibrational phase contrast detection to obtain imaging of imaginary components of third-order nonlinear susceptibility in a coherent anti-Stokes Raman scattering （CARS） microscope with full suppression of the non-resonant background. This technique is based on the unique ability of recovering the phase of the generated CARS signal based on holographic recording. By capturing the phase distributions of the generated CARS field from the sample and from the environment under resonant illumination, we demonstrate the retrieval of imaginary components in the CARS microscope and achieve background free coherent Raman imaging.

Theoretical and experimental investigations of coherent phonon dynamics in sapphire crystal using femto-second time-resolved coherent anti-Stokes Raman scattering

We report on the theoretical and the experimental investigations of the coherent phonon dynamics in sapphire crystal using the femtosecond time-resolved coherent anti-Stokes Raman scattering （fs-CARS） technique. The temporal chirped white-light continuum （WLC） is used for the Stokes pulse, therefore we can perform the selective excitation of the phonon modes without using a complicated laser system. The expected quantum beat phenomenon is clearly observed. The theoretical formulas consist very well with the experimental results. The dephasing times of the excited phonon modes, the wavenumber difference, and the phase shift between the simultaneously excited modes are obtained and discussed. This work opens up a way to study directly high-frequency coherent phonon dynamics in bulk crystals on a femtosecond time scale and is especially helpful for understanding the nature of coherent phonons.

Analysis of detection limit to time-resolved coherent anti-Stokes Raman scattering nanoscopy

In the implementation of CARS nanoscopy, signal strength decreases with focal volume size decreasing. A crucial problem that remains to be solved is whether the reduced signal generated in the suppressed focal volume can be detected. Here reported is a theoretical analysis of detection limit （DL） to time-resolved CARS （T-CARS） nanoscopy based on our proposed additional probe-beam-induced phonon depletion （APIPD） method for the low concentration samples. In order to acquire a detailed shot-noise limited signal-to-noise （SNR） and the involved parameters to evaluate DL, the T-CARS process is described with full quantum theory to estimate the extreme power density levels of the pump and Stokes beams determined by saturation behavior of coherent phonons, which are both actually on the order of ~ 109 W/cm2. When the pump and Stokes intensities reach such values and the total intensity of the excitation beams arrives at a maximum tolerable by most biological samples in a certain suppressed focal volume （40-nm suppressed focal scale in APIPD method）, the DL correspondingly varies with exposure time, for example, DL values are 103 and 102 when exposure times are 20 ms and 200 ms respectively.

Supercontinuum fiber laser-based coherent anti-Stokes Raman scattering microscopy for label-free chemical imaging

Coherent anti-Stokes Raman scattering(CA RS)microscopy can resolve the chemical compo-nents and distribution of living biological systems in a label-firee manner and is favored in several disciplines.Current CA RS microscopes typically use bulky,high-performance solid-state lasers,which are expensive and sensitive to environmental changes.With their relatively low cost and environmental sensitivity,supercontinum fiber(SF)lasers with a small footprint have found increasing use in biomedical applications.Upon these features,in this paper,we homebuilt a low-cost CARS microscope based on a SF laser module(scCA RS microscope).This SF laser module is specially customized by adding a time synchronized seed source channel to the SF laser to form a dual-channel output laser.The performance of the scCARS microscope is evaluated with dimethyl sulfoxide,whose results confirm a spatial resolution of better than 500nm and a detection sensitivity of millimolar concentrations.The dual-color imaging capability is further demonstrated by imaging different species of mixed microspheres.We finally explore the potential of our scCARS microscope by mapping lipid droplets in different cancer cells and corneal stromal lenses.

Selective Excitation of Two-pulse Femtosecond Coherent Anti-Stokes Raman Scattering in a Mixture

In this paper, we experimentally study the selective excitation of two-pulse femtosecond coherent anti-Stokes Raman scattering (CARS) in a mixture of dibromomethane (CH2Br2) and chloroform (CHCl3) by adaptive pulse shaping based on genetic algorithm. Second harmonic generation frequency-resolved optical gating (SHG-FROG) traces indicate that the spectral amplitude and phase of the optimal pulse are both modulated. Finally, we discuss the physical mechanism for the selective excitation of femtosecond CARS based on the retrieved information from SHG-FROG traces.

High enhancement factor of Au nano triangular prism structure for surface enhanced coherent anti-Stokes Raman scattering

Coherent anti-Stokes Raman scattering spectroscopy（CARS） is a well-known detecting tool in biosensing and nonlinear spectroscopy. It can provide a non-invasive alternative without the need for exogenous labels,while the enhancement factor for surface plasmon resonances（SPR） are extensively used to increase the local field close to the oscillators and which can obtain high enhancement. In this work, we investigate the enhancement factor of our structure for surface-enhanced coherent anti-Stokes Raman scattering. The absorption spectrum of the structure has been studied, a wide range of absorption has been realized. The enhancement can be as high as 10^（16） over standard CARS. Our design is very useful for improving the enhancement factor of surface-enhanced coherent anti-Stokes Raman scattering.

Coherent Raman scattering imaging of lipid metabolism in cancer

Cancer cells dysregulate lipid metabolism to accelerate energy production and biomolecule synthesis for rapid growth.Lipid metabolism is highly dynamic and intrinsically heterogeneous at the single cell level.Although°uorescence microscopy has been commonly used for cancer research,bulky°uorescent probes can hardly label small lipid molecules without perturbing their biological activities.Such a challenge can be overcome by coherent Raman scattering(CRS)microscopy,which is capable of chemically selective,highly sensitive,submicron resolution and high-speed imaging of lipid molecules in single live cells without any labeling.Recently developed hyperspectral and multiplex CRS microscopy enables quantitative mapping of various lipid metabolites in situ.Further incorporation of CRS microscopy with Raman tags greatly increases molecular selectivity based on the distinct Raman peaks well separated from the endogenous cellular background.Owing to these unique advantages,CRS microscopy sheds new insights into the role of lipid metabolism in cancer development and progression.This review focuses on the latest applications of CRS microscopy in the study of lipid metabolism in cancer.

Effect of CC Coherent Vibration on Relative Raman Scattering Cross Sections of All-trans β-Carotene

We have determined the Raman scattering cross sections（RSCSs） of fl-carotene for C=C and C-C stretching modes, with the 1444 cm^-1 Raman band of cyclohexane as internal standard, in different solvents at low concentrations by measuring Raman intensity. The results show that RSCSs of β-carotene were 10^6-10^7 times larger than the general RSCSs, we analyzed that this enhancement was caused not only by the resonance Raman effect but also by nonlinear coherent CC vibration in aqueous β-carotene. Moreover, overtone and combinations of it were also observed and their intensities were 10%-20% of those of their fundamentals when β-carotene was dissolved in non-polar solvents, respectively.

Stimulated Raman scattering microscopy on biological cellular machinery

Beneting from the developments of advanced optical microscopy techniques,the mysteries of biological functions at the cellular and subcellular levels have been continuously revealed.Stimulated Raman scattering(SRS)microscopy is a rapidly growing technique that has attracted broad attentions and become a powerful tool for biology and biomedicine,largely thanks to its chemical specicity,high sensitivity and fast image speed.This review paper introduces the principles of SRS,discusses the technical developments and implementations of SRS microscopy,then highlights and summarizes its applications on biological cellular machinery andnally shares our visions of potential breakthroughs in the future.

Stimulated Raman scattering microscopy for rapid brain tumor histology

Rapid histology of brain tissues with sufficient diagnostic information has the great potential to aid neurosurgons during operations.Stimulated Raman Scattering(SRS)microscopy is an emerging label-free imaging technique,with the intrinsic chemical resolutions to delineate brain tumors from normal tissues without the nood of time-consuming tissue processing.Growing number of studies have shown SRS as a“virtual histology"tool for rapid diagnosis of various types of brain tumors.In this review,we focus on the basic principles and current developments of SRS microscopy,as well as its applications for brain tumor imaging.

Improvement in the calculation of anti-Stokes energy transfer and experimental justification based on Er_(0.01)Yb_xY_(1 0.01 x)VO_4 crystal

The improvement on the calculation of anti-Stokes energy transfer rate is studied in the present work. The additional proportion coefficient between Stokes and anti-Stokes light intensities of quantum Raman scattering theory as compared with the classical Raman theory is introduced to successfully describe the anti-Stokes energy transfer. The theoretical formula for the improvement on the calculation of anti-Stokes energy transfer rate is derived for the first time in this study. The correctness of introducing coefficient exp{△E/kT} from well-known Raman scatter theory is demonstrated also. Moreover, the experimental lifetime measurement in Er0.01YbxY1-0.01-xVO4 crystal is performed to justify the validity of our important improvement in the original phonon-assisted energy transfer theory for the first time.

飞秒相干反斯托克斯拉曼散射光谱测温研究进展

当今世界大约90%的能量供应都是由燃烧生成的。在燃烧场中,火焰的温度影响着场中各种组分链式反应的途径和浓度,获取燃烧场温度信息可以为提高燃料燃烧效率,改进燃烧装置的设计提供重要的支撑依据。随着我国在航空、航天和航海这类高端制造业领域的不断发展,各种大型燃气轮机和超声速发动机的研发进入加速期,此类燃烧装置产生的火焰具有高温、高压、湍流超声速和持续时间短等特点。传统的接触式测温法难以对这类湍流燃烧场进行温度测量,近年以激光光谱法为代表的非接触式测温技术逐渐走向成熟,并获得了广泛地应用。与超短脉冲相结合的飞秒相干反斯托克斯拉曼散射光谱测温技术凭借可提供高时间分辨率(每秒可提供上千个测温数据)、高测温精度和高测温灵敏度等优势而被应用到各种高温、湍流等复杂燃烧场景温度诊断中。文章概述了飞秒相干反斯托克斯拉曼散射测温技术的基本原理,综述了该技术在稳态火焰、加热气体、模拟燃气轮机等燃烧环境中测温工作的研究进展,简要介绍了飞秒时间分辨相干反斯托克斯拉曼光谱的研究和应用,着重介绍了可以实现毫秒量级时间分辨率的飞秒啁啾探测脉冲相干反斯托克斯拉曼散射测温技术和混合飞秒/皮秒相干反斯托克斯拉曼散射测温技术的基本原理和应用进展。指出了三种测温技术的优缺点,并提出飞秒相干反斯托克斯拉曼散射测温技术目前需要关注并解决的技术问题,主要为在高温高压湍流燃烧等极端条件下实现高精度CARS光谱高保真反演出温度信息,以及高温高压湍流燃烧场极端条件下如何获得高信噪比CARS信号的问题。展望了今后的发展趋势:通过高时间分辨的测量,获得湍流火焰中温度的瞬时演化规律,并建立各种复杂火焰的温度演化信息数据库,为研究各种发动机机理提供支撑。

非平衡等离子体流场相干反斯托克斯拉曼散射光谱计算及振转温度测量

高温非平衡问题是高超声速流动中最基本的科学问题之一,而热力学非平衡特性的准确表征是理解高温非平衡问题和高超声速空气动力学的基础,如何准确可靠地表征流场的热力学非平衡特性是解决高超声速飞行器在稀薄流域高温非平衡问题的关键.本文基于相干反斯托克斯拉曼散射基本原理,开发了面向非平衡流场的振转温度反演算法,并在宽温度范围静态环境开展验证.搭建了非平衡等离子体流场相干反斯托克斯拉曼散射测温实验平台并开展实验验证,结果表明微波等离子体处于热力学非平衡状态,并且振动温度和转动温度与微波功率成正比,而热力学非平衡度与微波功率成反比,当微波功率从80W增加至180 W时,等离子体电子数密度增加,中性粒子通过与电子碰撞获得能量使振动温度从(2201±43)K增加至(2452±56)K、转动温度从(382±20)K增加至(535±49)K;而处于振动激发态的分子通过振动-平动弛豫过程(对于N2分子弛豫速率与温度成正比)将部分振动能转化为平动能,导致振动温度与转动温度的差异降低,等离子体热力学非平衡度从0.83降低至0.78.

锥形微纳光纤激发相干反斯托克斯拉曼散射光谱研究

从数值仿真和实验测量方面验证了使用锥形微纳光纤代替聚焦物镜产生相干拉曼散射信号的可行性。通过数值计算以及实验测量分析了超短脉冲在锥形微纳光纤中的传输特性,证明锥区长度为5cm的锥形微纳光纤可以有效保证超短脉冲在其中传输时的时域和谱域特性,并且功率衰减较小,850~1100nm波长范围内的实测插入损耗最大值不超过1.05dB,平均值0.84dB。然后,使用锥形微纳光纤成功探测到环已烷在2853cm^(-1)位置处的拉曼共振峰,证明了使用锥形微纳光纤激发相干拉曼光谱的可行性。使用锥形微纳光纤激发相干拉曼光谱具有信号激发灵活方便,摆脱了传统空间光学的约束,为相干反斯托克斯拉曼散射(coherent anti-Stokes Raman scattering,CARS)系统在内窥成像领域和微创检测领域的发展提供了一种新的途径。