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Engineering And Application Of Ultrafast Laser Pulses And Filamentation In AirBarbieri, Nicholas 01 January 2013 (has links)
Continuing advances in laser and photonic technology has seen the development of lasers with increasing power and increasingly short pulsewidths, which have become available over an increasing range of wavelengths. As the availability of laser sources grow, so do their applications. To make better use of this improving technology, understanding and controlling laser propagation in free space is critical, as is understanding the interaction between laser light and matter. The need to better control the light obtained from increasingly advanced laser sources leads to the emergence of beam engineering, the systematic understanding and control of light through refractive media and free space. Beam engineering enables control over the beam shape, energy and spectral composition during propagation, which can be achieved through a variety of means. In this dissertation, several methods of beam engineering are investigated. These methods enable improved control over the shape and propagation of laser light. Laser-matter interaction is also investigated, as it provides both a means to control the propagation of pulsed laser light through the atmosphere, and provides a means to generation remote sources of radiation.
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Gas Phase Nonlinear and Ultrafast Laser SpectroscopyZiqiao Chang (17543487) 04 December 2023 (has links)
<p dir="ltr">The objective of this research is to advance the development and application of laser diagnostics in gas phase medium, which ranges from atmospheric non-reacting flows to turbulent reacting flows in high-pressure, high-temperature environments. Laser diagnostic techniques are powerful tools for non-intrusive and in-situ measurements of important chemical parameters, such as temperature, pressure, and species mole fractions, in harsh environments. These measurements significantly advance the knowledge across various research disciplines, such as combustion dynamics, chemical kinetics, and molecular spectroscopy. In this thesis, detailed theoretical models and experimental analysis are presented for three different techniques: 1. Chirped-probe-pulse femtosecond coherent anti-Stokes Raman scattering (CPP fs CARS); 2. Two-color polarization spectroscopy (TCPS); 3. Ultrafast-laser-absorption-spectroscopy (ULAS). The first chapter provides a brief survey of laser diagnostics, including both linear and nonlinear methods. The motivations behind the three studies covered in this dissertation are also discussed. </p><p dir="ltr">In the second chapter, single-shot CPP fs CARS thermometry is developed for the hydrogen molecule at 5 kHz. The results are divided into two parts. The first part concentrates on the development of H<sub>2</sub> CPP fs CARS thermometry for high-pressure and high-temperature conditions. The second part demonstrates the application of H<sub>2</sub> CPP fs CARS in a model rocket combustor at pressures up to 70 bar. In the first part, H<sub>2</sub> fs CARS thermometry was performed in Hencken burner flames up to 2300 K, as well as in a heated gas-cell at temperatures up to 1000 K. It was observed that the H<sub>2</sub> fs CARS spectra are highly sensitive to the pump and Stokes chirp. Chirp typically originates from optical components such as windows and polarizers. As a result, the pump delay is modeled to provide a shift to the Raman excitation efficiency curve. With the updated theoretical model, excellent agreement was found between the simulated and experimental spectra. The averaged error and precision are 2.8% and 2.3%, respectively. In addition, the spectral phase and pump delay determined from the experimental spectra closely align with the theoretical predictions. It is also found that pressure does not have significant effects on the H<sub>2</sub> fs CARS spectra up to 50 bar at 1000 K. The collision model provides excellent agreement with the experiment. This allows the use of low-pressure laser parameters for high-pressure thermometry measurements. In the second part, spatially resolved H<sub>2</sub> temperature was measured in a rocket chamber at pressures up to 70 bar. This is the first demonstration of fs CARS thermometry inside a high-pressure rocket combustor. These results highlight the potential of using H<sub>2</sub> CPP fs CARS thermometry to provide quantitative data in high-pressure experiments for the study of combustion dynamics and model validation efforts at application relevant operating conditions.</p><p dir="ltr">The third chapter presents the development of a TCPS system for the study of the NO (<i>A</i><sup>2</sup>Σ<sup>+</sup>-<i>X</i><sup>2</sup>Π) state-to-state collision dynamics with He, Ar, and N<sub>2</sub>. Two sets of TCPS spectra for 1% NO, diluted in different buffer gases at 295 K and 1 atm, were obtained with the pump beam tuned to the R<sub>11</sub>(11.5) and <sup>O</sup>P<sub>12</sub>(1.5) transitions. The probe was scanned while the pump beam was tuned to the line center. Collision induced transitions were observed in the spectra as the probe scanned over transitions that were not coupled with the pump frequency. The strength and structure of the collision induced transitions in the TCPS spectra were compared between the three colliding partners. Theoretical TCPS spectra, calculated by solving the density matrix formulation of the time-dependent Schrödinger wave equation, were compared with the experimental spectra. A collision model based on the modified exponential-gap law was used to model the rotational level-to-rotational level collision dynamics. An unique aspect of this work is that the collisional transfer from an initial to a final Zeeman state was modeled based on the difference in the cosine of the rotational quantum number <i>J</i> projection angle with the z-axis for the two Zeeman states. Rotational energy transfer rates and Zeeman state collisional dynamics were varied to obtain good agreement between theory and experiment for the two different TCPS pump transitions and for the three different buffer gases. One key finding, in agreement with quasi-classical trajectory calculations, is that the spin-rotation changing transition rate in the <i>A</i><sup>2</sup>Σ<sup>+</sup> level of NO is almost zero for rotational quantum numbers ≥ 8. It was necessary to set this rate to near zero to obtain agreement with the TCPS spectra. </p><p dir="ltr">The fourth chapter presents the development and application of a broadband ULAS technique operating in the mid-infrared for simultaneous measurements of temperature, methane (CH<sub>4</sub>), and propane (C<sub>3</sub>H<sub>8</sub>) mole fractions. Single-shot measurements targeting the C-H stretch fundamental vibration bands of CH<sub>4</sub> and C<sub>3</sub>H<sub>8</sub> near 3.3 μm were acquired in both a heated gas cell up to ~650 K and laminar diffusion flames at 5 kHz. The average temperature error is 0.6%. The average species mole fraction error are 5.4% for CH<sub>4</sub>, and 9.9% for C<sub>3</sub>H<sub>8</sub>. This demonstrates that ULAS is capable of providing high-fidelity hydrocarbon-based thermometry and simultaneous measurements of both large and small hydrocarbons in combustion gases. </p>
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ULTRAFAST LASER ABSORPTION SPECTROSCOPY IN THE ULTRAVIOLET AND MID-INFRARED FOR CHARACTERIZING NON-EQUILIBRIUM GASESVishnu Radhakrishna (5930801) 23 April 2024 (has links)
<p dir="ltr">Laser absorption spectroscopy (LAS) is a widely used technique to acquire path-integrated measurements of gas properties such as temperature and mole fraction. Although extremely useful, the application of LAS to study heterogeneous combustion environments can be challenging. For example, beam steering can be one such challenge that arises during measurements in heterogeneous combustion environments such as metallized propellant flames or measurements at high-pressure conditions. The ability to only obtain path integrated measurements has been a major challenge of conventional LAS techniques, especially in characterizing combustion environments with a non-uniform thermo-chemical distribution along the line of sight (LOS). Additionally, simultaneous measurements of multiple species using LAS with narrow-bandwidth lasers often necessitates employing multiple light sources. Aerospace applications, such as characterizing hypersonic flows may require ultrashort time resolution to study fast-evolving chemistry. Similarly, atmospheric entry most often requires measurements of atoms and molecules that absorb at wavelengths ranging from ultraviolet to mid-infrared. The availability of appropriate light sources for such measurements has been limited. In the past, several researchers have come up with diagnostic techniques to overcome the above-mentioned challenges to a certain extent. Most often, these solutions have been need-based while compromising on other diagnostic capabilities. Therefore, LAS diagnostics capable of acquiring broadband measurements with ultrafast time resolution and the ability to acquire measurements at wavelengths in ultraviolet through mid-infrared is required to study advanced combustion systems and for the development of advanced aerospace systems for future space missions. Ultrafast laser absorption spectroscopy is one such technique that provides broadband measurements, enabling simultaneous multi-species and high-pressure measurements. The light source utilized for ULAS provides the ultrafast time resolution necessary for resolving fast-occurring chemistry and more importantly the ability to acquire measurements at a wide range of wavelengths ranging from ultraviolet to far-infrared. The development and application of ULAS for characterizing propellant flames and hypersonic flows under non-equilibrium conditions by overcoming the above-mentioned challenges is presented here. </p><p>This work describes the development of a single-shot ultrafast laser absorption spectroscopy (ULAS) diagnostic for simultaneous measurements of temperature and concentrations of CO, NO, and H<sub>2</sub>O in flames and aluminized fireballs of HMX (C<sub>4</sub>H<sub>8</sub>N<sub>8</sub>O<sub>8</sub>). Ultrashort (55 fs) pulses from a Ti:Sapphire oscillator emitting near 800 nm were amplified and converted into the mid-infrared through optical parametric amplification (OPA) at a repetition rate of 5 kHz. Ultimately, pulses with a spectral bandwidth of ≈600 cm<sup>-1</sup> centered near 4.9 µm were utilized in combination with a mid-infrared spectrograph to measure absorbance spectra of CO, NO, and H<sub>2</sub>O across a 30 nm bandwidth with a spectral resolution of 0.3 nm. The gas temperature and species concentrations were determined by least-squares fitting simulated absorbance spectra to measured absorbance spectra. Measurements of temperature, CO, NO, and H<sub>2</sub>O were acquired in an HMX flame burning in air at atmospheric pressure and the measurements agree well with previously published results. Measurements were also acquired in fireballs of HMX with and without 16.7 wt% H-5 micro-aluminum. Time histories of temperature and column densities are reported with a 1-σ precision of 0.4% for temperature and 0.3% (CO), 0.6% (NO), and 0.5% (H<sub>2</sub>O), and 95% confidence intervals (C.I.) of 2.5% for temperature and 2.5% (CO), 11% (NO), and 7% (H<sub>2</sub>O), thereby demonstrating the ability of ULAS to provide high-fidelity, multi-parameter measurements in harsh combustion environments. The results indicate that the addition of the micron-aluminum increases the fireball peak temperature by ≈100 K and leads to larger concentrations of CO. The addition of aluminum also increases the duration fireballs remain at elevated temperatures above 2000 K.</p><p dir="ltr">Next, the application of ULAS for dual-zone temperature and multi-species (CO, NO, H<sub>2</sub>O, CO<sub>2</sub>, HCl, and HF) measurements in solid-propellant flames is presented. ULAS measurements were acquired at three different central wavelengths (5.121 µm, 4.18 µm, and 3.044 µm) for simultaneous measurements of temperature and: 1) CO, NO, and H<sub>2</sub>O, 2) CO<sub>2</sub> and HCl, and 3) HF and H<sub>2</sub>O. Absorption measurements with a spectral resolution of 0.35 nm and bandwidth of 7 cm<sup>-1</sup>, 18 cm<sup>-1</sup>, and 35 cm<sup>-1</sup>, respectively were acquired. In some cases, a dual-zone absorption spectroscopy model was implemented to accurately determine the gas temperature in the hot flame core and cold flame boundary layer via broadband absorption measurements of CO<sub>2</sub>, thereby overcoming the impact of line-of-sight non-uniformities. Results illustrate that the hot-zone temperature of CO<sub>2</sub> agrees well with the equilibrium flame temperature and single-zone thermometry of CO, the latter of which is insensitive to the cold boundary layer due to the corresponding oxidation of CO to CO<sub>2</sub>.</p><p dir="ltr">The initial development and implementation of an ultraviolet and broadband ultrafast-laser-absorption-imaging (UV-ULAI) diagnostic for one dimensional (1D) imaging of temperature and CN via its <i>B</i><sup>2</sup>Σ<sup>+</sup>←<i>X</i><sup>2</sup>Σ<sup>+ </sup>absorption bands near 385 nm. The diagnostic was demonstrated by acquiring single-shot measurements of 1D temperature and CN profiles in HMX flames at a repetition rate of 25 Hz. Ultrashort pulses (55 fs) at 800 nm were generated using a Ti:Sapphire oscillator and then amplification and wavelength conversion to the ultraviolet was carried out utilizing an optical parametric amplifier and frequency doubling crystals. The broadband pulses were spectrally resolved using a 1200 l/mm grating and imaged on an EMCCD camera to obtain CN absorbance spectra with a resolution of ≈0.065 nm and a bandwidth of ≈4 nm (i.e. 260 cm<sup>-1</sup>). Simulated absorbance spectra of CN were fit to the measured absorbance spectra using non-linear curve fitting to determine the gas properties. The spatial evolution of gas temperature and CN concentration near the burning surface of an HMX flame was measured with a spatial resolution of ≈10 µm. 1D profiles of temperature and CN concentration were obtained with a 1-σ spatial precision of 49.3 K and 4 ppm. This work demonstrates the ability of UV-ULAI to acquire high-precision, spatially resolved absorption measurements with unprecedented temporal and spatial resolution. Further, this work lays the foundation for ultraviolet imaging of numerous atomic and molecular species with ultrafast time resolution.</p><p dir="ltr">Ultraviolet ULAS was applied to characterize the temporal evolution of non-Boltzmann CN (<i>X</i><sup>2</sup>Σ<sup>+</sup>) formed behind strong shock waves in N<sub>2</sub>-CH<sub>4</sub> mixtures at conditions relevant to entry into Titan's atmosphere. An ultrafast (femtosecond) light source was utilized to produce 55 fs pulses near 385 nm at a repetition rate of 5 kHz and a spectrometer with a 2400 lines/mm grating was utilized to spectrally resolve the pulses after passing through the Purdue High-Pressure Shock Tube. This enabled broadband single-shot absorption measurements of CN to be acquired with a spectral resolution and bandwidth of ≈0.02 nm and ≈6 nm (≈402 cm<sup>-1</sup> at these wavelengths), respectively. A line-by-line absorption spectroscopy model for the <i>B</i><sup>2</sup>Σ<sup>+</sup>←<i>X</i><sup>2</sup>Σ<sup>+</sup> system of CN was developed and utilized to determine six internal temperatures (two vibrational temperatures, four rotational) of CN from the (0,0), (1,1), (2,2) and (3,3) absorption bands. Measurements were acquired behind reflected shock waves in 5.65% CH<sub>4</sub> and 94.35% N<sub>2</sub> with an initial pressure of 1.56 mbar and incident shock speed of ≈2.1 km/s. For this test condition, the chemically and vibrationally frozen temperature of the mixture behind the reflected shock was 5000 K and the pressure was 0.6 atm. The high repeatability of the shock-tube experiments (0.3% variation in shock speed across tests) enabled multi-shock time histories of CN mole fraction and six internal temperatures to be acquired with a single-shot time resolution of less than 1 ns. The measurements revealed that CN <i>X</i><sup>2</sup>Σ<sup>+</sup> is non-Boltzmann rotationally and vibrationally for greater than 200 µs, thereby strongly suggesting that chemical reactions are responsible for the non-Boltzmann population distributions. </p><p><br></p>
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Adaptive techniques for ultrafast laser material processingStoian, Razvan 18 November 2008 (has links) (PDF)
Le besoin d'une très grande précision lors du traitement des matériaux par laser a fortement encouragé le développement des études de l'effet des impulsions ultra brèves pour la structuration des matériaux à une échelle micro et nano métrique. Une diffusion d'énergie minimale et une forte non linéarité de l'interaction permet un important confinement énergétique à des échelles les plus petites possibles. La possibilité d'introduire des changements de phases rapides et même de créer de nouveaux états de matière ayant des propriétés optimisées et des fonctions améliorées donne aux impulsions ultra brèves de sérieux arguments pour être utilisées dans des dispositifs très précis de transformation et de structuration des matériaux. L'étude de ces mécanismes de structuration et, en particulier, de leurs caractéristiques dynamiques, est une clé pour l'optimisation de l'interaction laser-matière suivant de nombreux critères utiles pour les procédés laser : efficacité, précision, qualité. Ce mémoire synthétise les travaux de l'auteur sur l'étude statique et dynamique du dépôt d'énergie ultra rapide, avec application aux procédés laser. La connaissance de la réponse dynamique des matériaux après irradiation laser ultra brève montre que les temps de relaxation pilotent l'interaction lumière-matière. Il est alors possible d'adapter l'énergie déposée à la réponse du matériau en utilisant les toutes récentes techniques de mise en forme spatio temporelle de faisceaux. Un couplage optimal de l'énergie donne la possibilité d'orienter la réponse du matériau vers un résultat recherché, offrant une grande flexibilité de contrôle des procédés et, sans doute, la première étape du développement de procédés « intelligents ».
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