Global ETD Search

81	Ultrafast Raman Loss Spectroscopic Investigations of Excited State Structural Dynamics of Bis(phenylethynyl)benzene and trans-Stilbene Mallick, Babita January 2017 (has links) (PDF) The subject of this thesis is the design and development of a unified set up for femtosecond transient absorption and ultrafast Raman loss spectroscopy and demonstrate its potential in capturing the ultrafast photophysical and photochemical processes with excellent time and frequency resolution. Ultrafast spectroscopy has been serving as a powerful tool for understanding the structural dynamical properties of molecules in the condensed and gas phase. The advent of ultrashort pulses with their high peak power enables the laser spectroscopic community to study molecular reaction dynamics and photophysics that happen at extremely short timescales, ranging from picosecond to femtosecond. These processes can be measured with extremely high time resolution, which helps to resolve the under-lying molecular process. But in order to understand the global mechanism of the underlying molecular processes, we have to resolve the nuclear dynamics with the proper frequency resolution. However, achieving both, time and frequency resolutions simultaneously is not possible according to the Heisenberg uncertainty principle. Later, this limitation was overcome by femtosecond stimulated Raman spectroscopy (FSRS), a third order non-linear Raman spectroscopy. In this thesis we introduced the ultrafast Raman loss spectroscopic (URLS) technique which is analogous to FSRS, offering the modern ultrafast community to resolve molecular processes with better signal-to-noise ratio along with proper time and frequency resolution. We demonstrate the experimental procedure including the single shot detection scheme to measure whitelight background, ground state Ra-man, transient absorption and transient Raman in shot-to-shot detection fashion. URLS has been applied to understand the excited state planarization dynamics of 1,4-bis(phenylethynyl)benzene (BPEB) in different solvents. In addition, excitation wavelength dependent conformational reorganization dynamics of different sub-sets of thermally activated ground state population of BPEB are also discussed. Using the same techniques along with femtosecond transient absorption, we demonstrate the ultrafast vibrational energy transfer and the role of coherent oscillations of low frequency vibrations on the solution phase photo-isomerization of trans-stilbene from an optically excited state. The effects of solvents on the coherent nuclear motion are also discussed in the context of reaction rates. 2 Bis(phenylethynyl)benzene (BPEB) Ultrafast Raman Loss Spectroscopy (URLS) Vibrational Spectroscopy Ultrafast Spectroscopy trans-Stilbene Time-Resolved Spectroscopy Time Resolved Absorption Femtosecond Stimulated Raman Scattering Femtosecond Transient Absorption Ultrafast Raman Loss Study Raman Loss Spectroscopic Studies Inorganic and Physical Chemistry
82	NONLINEAR ULTRAFAST-LASER SPECTROSCOPY OF GAS-PHASE SPECIES AND TEMPERATURE IN HIGH-PRESSURE REACTING FLOWS Kazi Arafat Rahman (8085560) 05 December 2019 (has links) <p>Ultrafast laser-based diagnostic techniques are powerful tools for the detailed understanding of highly dynamic combustion chemistry and physics. The ultrashort pulses provide unprecedented temporal resolution along with high peak power for broad spectral range−ideal for nonlinear signal generation at high repetition rate−with applications including next-generation combustors for gas turbines, plasma-assisted combustion, hypersonic flows and rotating detonation engines. The current work focuses on advancing (i) femtosecond (fs) two-photon laser-induced fluorescence, and (ii) hybrid femtosecond/picosecond vibrational and rotational coherent anti-Stokes Raman scattering (fs/ps RCARS and VCARS) to higher pressures for the first time. </p><p>Quantitative single-laser-shot kHz-rate concentration measurements of key atomic (O-atom) and molecular (CO) species is presented using femtosecond two-photon laser-induced fluorescence (TP-LIF) for a range of equivalence ratios and pressures in diffusion flames. A multitude of signal-interfering sources and loss mechanisms−relevant to high-pressure fs TP-LIF applications−are also quantified up to 20 atm to ensure high accuracy. The pressure scaling of interferences take into account degradation, attenuation and wave-front distortion of the excitation laser pulse; collisional quenching and pressure dependent transition line-broadening and shifting; photolytic interferences; multi-photon ionization; stimulated emission; and radiation trapping. </p><p>Hybrid fs/ps VCARS of N<sub>2</sub> is reported for interference-free temperature measurement at 1300-2300 K in high-pressure, laminar diffusion flames up to 10 atm. A time asymmetric probe pulse allowed for detection of spectrally resolved CARS signals at probe delays as early as ~200-300 fs while being independent of collisions for the full range of pressures and temperatures. Limits of collisional independence, accuracy and precision of the measurement is explored at various probe-pulse delays, pressures and temperatures. </p><p> </p><p>Additionally, a novel all diode-pumped Nd:YAG amplifier design is presented for generation of time-synchronized ps-probe pulses for hybrid fs/ps RCARS of N<sub>2</sub>. High-energy, nearly transform-limited, single-mode, chirp-free ps probe-pulses are generated at variable pulsewidths. The detailed architecture and characterization of the laser is presented. kHz-rate RCARS thermometry is presented up to 2400 K. Excellent spatial, spectral, and temporal beam quality allowed for fitting the theoretical spectra with a simple Gaussian model for the probe pulse with temperature accuracies of 1-2%. </p> <p><br></p> Aerospace Engineering Mechanical Engineering Nonlinear Optics and Spectroscopy combustion diagnostic laser diagnostics nonlinear spectroscopy high-pressure flames two-photon laser-induced fluorescence Multiphoton processes Optical amplifiers Self-focusing Ultrafast spectroscopy Ultrafast lasers
83	Imagerie ultrarapide à l’échelle nanométrique par diffraction XUV cohérente / Ultrafast coherent XUV diffractive imaging at nanometer scale Ge, Xunyou 11 December 2012 (has links) Imager des objets non-périodiques à une échelle nanométrique et à une échelle femto seconde est un vrai challenge à notre époque. Les techniques d’imagerie « sans lentille » sont des moyens puissants pour répondre à ce besoin. En utilisant des sources ultrarapide (~fs) et cohérente (ex. laser à électron libre ou harmoniques d’ordres élevés), ces techniques nous permettent de reconstruire des objets à partir de leur figure de diffraction, remplaçant les optiques conventionnelles du système d’imagerie par un algorithme informatique. Dans ce travail de thèse, je présent des expériences d’imageries en utilisant un rayonnement extrême-UV (15~40 nm) produit par la génération d’harmoniques d’ordre élevé d’un laser infrarouge puissant. Ce manuscrit est constitué d’une introduction, un chapitre de background théorique, trois chapitres de travail de thèse et une conclusion générale avec perspectives. La première partie du travail de thèse porte sur les développements et caractérisations de la ligne de lumière avec l’objectif de générer maximum de photons harmoniques cohérents avec un front d’onde plat. La deuxième partie est consacrée aux expériences et analyses de trois techniques d’imageries « sans lentille » : Imagerie par diffraction cohérente (CDI), Holographie par la transformée de Fourier (FTH) et Holographie avec références étendues (HERALDO). Ces derniers nous permettent de reconstruire des objets avec une résolution spatiale de 78 nm dans le cas de CDI et de 112 nm dans le cas de HERALDO, tous les deux avec une résolution temporaire de 20 fs. La troisième partie est une première application physique de l’imagerie sur la ligne harmonique. Il s’agit des études statiques et dynamiques de nano-domaines magnétique avec une résolution spatiale sub-100 nm à l’échelle femto seconde. Perspective des techniques d’imagerie 3D et développement potentiel de la ligne d’harmoniques sont présentés à la fin. / Ultrafast imaging of isolated objects with nanometric spatial resolution is a great challenge in our time. The lensless imaging techniques have shown great potential to answer this challenge. In lensless imaging, one can reconstruct sample images from their diffraction patterns with computational algorithms, which replace the conventional lens systems. Using ultrafast and coherent light sources, such as free electron laser and high order harmonics, one can investigate dynamic phenomena at the femtosecond time scale. In this thesis work, I present the lenless imaging experiments using XUV radiation provided by a laser driven high order harmonic beamline. The manuscript is composed of an introduction, a chapter of theoretical background, three chapters of main research work and a general conclusion with perspectives. The first part of this work concerns the development of the harmonic beamline to optimize the illumination condition for lensless imaging. The second part concentrates on the imaging techniques: the Coherent Diffraction Imaging (CDI), the Fourier Transform Holography (FTH) and the Holography using extended references (HERALDO). The reconstructions have achieved 78 nm spatial resolution in case of CDI and 112 nm resolution in case of HERALDO, both in single-shot regime corresponding to a temporal resolution of 20 fs. The third part presents the first physical application on the harmonic beamline using the lensless imaging. Samples with magnetic nano-domains have been studied with sub-100 nm spatial resolution, which paves the way for ultrafast magnetic dynamic studies. At the end, single-shot 3D imaging and further beamline development have been discussed. Diffraction cohérente Imagerie sans lentille Source UV-X Filtrage modal Holographie par transformée de Fourier Références holographiques étendues Rapport signal sur bruit Diffusion élastique résonante Sonde simple tir Spectroscopie ultrarapide Nano-magnétisme Coherent diffraction Lensless imaging High order harmonics generation XUV source Modal filtering Fourier transform holography Extended references Signal to noise ratio Resonant elastic scattering Single shot probing Ultrafast spectroscopy Nanomagnetism
84	Ultrafast exciton relaxation in quasi-one-dimensional perylene derivatives Engel, Egbert 30 January 2006 (has links) This thesis deals with exciton relaxation processes in thin polycrystalline films and matrix-isolated molecules of the perylene derivatives PTCDA (3,4,9,10-perylenetetracarboxylic dianhydride) and MePTCDI (N,N'-dimethylperylene-3,4,9,10-dicarboximide). Using femtosecond pump-probe spectroscopy, transient absorption spectra, excitonic relaxation in the lowest excited state subsequent to excitation, and exciton-exciton interaction and annihilation at high excitation densities have been addressed. Transient absorption spectroscopy in the range 1.2eV-2.6eV has been applied to thin polycrystalline films of PTCDA and MePTCDI and to solid solutions of PTCDA and MePTCDI molecules (monomers) in a SiO2 matrix. We are able to ascribe the respective signal contributions to ground state bleaching, stimulated emission, and excited state absorption. Both systems exhibit broad excited-state absorption features below 2.0eV, with dominant peaks between 1.8eV and 2.0eV. The monomer spectra can be consistently explained by the results of quantum-chemical calculations on single molecules, and the respective experimental polarization anisotropies for the two major transitions agree with the calculated polarizations. Dimer calculations allow to qualitatively understand the trends visible in the experimental results from monomers to thin films. The broad excited state absorption band between 1.8eV and 2.0eV allows to probe the population dynamics in the first excited state of thin films. We show that excitons created at the Gamma point relax towards the border of the Brillouin zone on a 100fs time scale in both systems. Excitonic relaxation is accelerated by increase of temperature and/or excitation density, which is attributed to stimulated phonon emission during relaxation in k-space. Lower and upper limits of the intraband relaxation time constants are 25fs (resolution limit) and 250fs (100fs) for PTCDA (MePTCDI). These values agree with the upper limit for the intraband relaxation time of 10ps, evaluated from time-resolved luminescence measurements. While the luminescence anisotropy is in full accordance with the predictions made by a luminescence anisotropy model being consistent with the exciton model of Davydov-split states, the pump-probe anisotropy calls for an explanation beyond the models presently available. At excitation densities 10^(19)cm^(-3), the major de-excitation mechanism for the relaxed excitons is exciton-exciton annihilation, resulting in a strongly reduced exciton life time. Three different models for the microscopic behavior have been tested: a diffusion-limited annihilation model in both three and one dimensions (with diffusion constant D as fit parameter) as well as a long-range single-step Förster-type annihilation model (with Förster radius RF as fit parameter). For PTCDA, the latter two, being structurally equivalent, allow to fit a set of multiexponential decay curves for multiple initial exciton densities with high precision. In contrast, the three-dimensional diffusion-limited model is clearly inferior. For all three models, we extract annihilation rates, diffusion constants and diffusion lengths (or Förster radii), for both room and liquid helium temperature. Temperature dependence and orders of magnitude of the obtained parameters D or RF correspond to the expectations. For MePTCDI, the 1D and the Förster model are in good agreement for a smaller interval of excitation densities. For a initial exciton densities higher than 5 x 10^(19)cm^(-3), the 3D model performs significantly better than the other two. info:eu-repo/classification/ddc/530 ddc:530
85	Novel tools for ultrafast spectroscopy Jarvis, Thomas William 06 February 2012 (has links) Exciton dynamics in semiconductor nanostructures are dominated by the effects of many-body physics. The application of coherent spectroscopic tools, such as two-dimensional Fourier transform spectroscopy (2dFTS), to the study of these systems can reveal signatures of these effects, and in combination with sophisticated theoretical modeling, can lead to more complete understanding of the behaviour of these systems. 2dFTS has previously been applied to the study of GaAs quantum well samples. In this thesis, we outline a precis of the technique before describing our own experiments using 2dFTS in a partially collinear geometry. This geometry has previously been used to study chemical systems, but we believe these experiments to be the first such performed on semiconductor samples. We extend this technique to a reflection mode 2dFTS experiment, which we believe to be the first such measurement. In order to extend the techniques of coherent spectroscopy to structured systems, we construct an experimental apparatus that permits us to control the beam geometry used to perform four-wave mixing reflection measurements. To isolate extremely weak signals from intense background fields, we extend a conventional lock-in detection scheme to one that treats the optical fields exciting the sample on an unequal footing. To the best of our knowledge, these measurements represent a novel spectroscopic tool that has not previously been described. / text Spectroscopy Ultrafast spectroscopy Ultra-fast spectroscopy Exciton Exciton dynamics Exciton optics Excitons Four-wave mixing Four wave mixing GaAs Gallium Arsenide Quantum well Semiconductor Acousto-optic Acousto optic Acousto-optic modulation Agile frequency Direct digital synthesis Lock-in detection Lock in detection Two-dimensional Two dimensional Fourier transform Multi-dimensional Multi dimensional Coherent Dephasing Relaxation Many body Many-body Physics Correlation Plasmon Surface plasmon Polariton Surface Hybrid Coupling Mode Grating Nanostructure Nano-structure Nano structure Reflection Mode geometry Transmission Variable Angle tuning Tunable Tuned Angle-tuning Angle-tunable Beam controllable Control

Page generated in 0.0528 seconds