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Amplification of laser-induced plasma in air is demonstrated utilizing resonant laser ionization and avalanche ionization. Molecular oxygen in air is ionized by a low-energy laser pulse employing (2 + 1) resonance-enhanced multi-photon ionization (REMPI) to generate seed electrons. Subsequent avalanche ionization of molecular oxygen and nitrogen significantly amplifies the laser-induced plasma. In this plasma-amplification effect, three-body attachments to molecular oxygen dominate the electron-generation and -loss processes, while either nitrogen or argon acts as the third body with low electron affinity. Contour maps of the electron density within the plasma obtained in O2/ N2 and O2/Ar gas mixtures are provided to show relative degrees of plasma amplification with respect to gas pressure and to verify that the seed electrons generated by O2 2 + 1 REMPI are selectively amplified by avalanche ionization of molecular nitrogen in a relatively low-pressure condition (≤100 Torr). Such plasma amplification occurring in air could be useful in aerospace applications at high altitude [ABSTRACT FROM AUTHOR]

Picosecond laser electronic excitation tagging (PLEET) is implemented in a large-scale wind tunnel for the first time. High-speed, unseeded velocimetry is performed in the NASA Langley 0.3 m transonic cryogenic tunnel; repetition rates up to 25 kHz are tested. Velocity measurements are assessed for accuracy and precision. Measurement errors vary in the range of 0.6%–1.2%, while the instrument precision is found to lie between 1.2 m s−1 and 2 m s−1 and exhibits little variation over the full operating range of the facility. An examination of the signal intensity reveals little to no thermodynamic dependence, and the signal lifetimes exhibit an inverse dependence on both pressure and temperature. The PLEET signal is demonstrated to be largely unaffected by buoyancy despite the large temperature rise. The velocity dynamic range of the measurements is found to be a factor of at least 200 in these experiments with the capacity to measure much higher velocities as well. The spatial resolution of the velocity measurements is found to lie between 2–2.7 mm, and the maximum frequency response is 12.5 kHz with the ability to resolve up to 50 kHz with the current measurement system. Overall measurement uncertainties in the streamwise velocity are found to lie between 4%–4.8% for high to low velocities, while the uncertainty in the transverse velocity is less than 6 m s−1. The measurement uncertainties are found to be dominated by systematic errors in the calibration procedure, which could be improved in future experiments. [ABSTRACT FROM AUTHOR]

Reacting flows and plasmas are prevalent in a wide array of systems involving defense, commercial, space, energy, medical, and consumer products. Understanding the complex physical and chemical processes involving reacting flows and plasmas requires measurements of key parameters, such as temperature, pressure, electric field, velocity, and number densities of chemical species. Time-resolved measurements of key chemical species and temperature are required to determine kinetics related to the chemical reactions and transient phenomena. Laser-based, noninvasive linear and nonlinear spectroscopic approaches have proved to be very valuable in providing key insights into the physico-chemical processes governing reacting flows and plasmas as well as validating numerical models. The advent of kilohertz rate amplified femtosecond lasers has expanded the multidimensional imaging of key atomic species such as H, O, and N in a significant way, providing unprecedented insight into preferential diffusion and production of these species under chemical reactions or electric-field driven processes. These lasers not only provide 2D imaging of chemical species but have the ability to perform measurements free of various interferences. Moreover, these lasers allow 1D and 2D temperature-field measurements, which were quite unimaginable only a few years ago. The rapid growth of the ultrafast-laser-based spectroscopic measurements has been fueled by the need to achieve the following when measurements are performed in reacting flows and plasmas. They are: (1) interference-free measurements (collision broadening, photolytic dissociation, Stark broadening, etc), (2) time-resolved single-shot measurements at a rate of 1–10 kHz, (3) spatially-resolved measurements, (4) higher dimensionality (line, planar, or volumetric), and (5) simultaneous detection of multiple species. The overarching goal of this article is to review the current state-of-the-art ultrafast-laser-based spectroscopic techniques and their remarkable development in the past two decades in meeting one or all of the above five goals for the spectroscopic measurement of temperature, number density of the atomic and molecular species, and electric field. [ABSTRACT FROM AUTHOR]

Absolute number densities of atomic species produced by nanosecond (ns)-duration, repetitively pulsed electric discharges are measured by two-photon-absorption laser-induced fluorescence (TALIF). Unique to this work is the development of femtosecond-laser-based TALIF (fs-TALIF) that offers a number of advantages over more conventional nanosecond (ns)-pulse-duration laser techniques, such as higher-fidelity quenching rate measurements over a wide pressure range, significantly reduced photolytic interference (including photo-dissociation and photo-ionization), ability to collect two-dimensional images of atomic-species number densities with high spatial resolution aided by higher signal level, and efficient and accurate measurements of atomic-species number densities due to the higher repetition rates of the laser. For full quantification of these advantages, atomic-oxygen TALIF signals are collected from an atmospheric-pressure plasma jet employing both ns- and fs-duration laser-excitation pulses and the results are compared and contrasted. [ABSTRACT FROM AUTHOR]

Femtosecond, two-photon-absorption laser-induced fluorescence (fs-TALIF) is employed to measure space- and time-resolved distributions of atomic hydrogen and oxygen in moderate-pressure, non-equilibrium, nanosecond-duration pulsed-discharge plasmas. Temporally and spatially resolved hydrogen and oxygen TALIF images are obtained over a range of low-temperature plasmas in mixtures of helium and argon at 100 Torr total pressure. The high-peak-intensity, low-average-energy fs pulses combined with the increased spectral bandwidth compared to traditional ns-duration laser pulses provide a large number of photon pairs that are responsible for the two-photon excitation, which results in an enhanced TALIF signal. Krypton and xenon TALIF are used for quantitative calibration of the hydrogen and oxygen concentrations, respectively, with similar excitation schemes being employed. This enables 2D collection of atomic-hydrogen and -oxygen TALIF signals with absolute number densities ranging from 2  ×  1012 cm−3 to 6  ×  1015 cm−3 and 1  ×  1013 cm−3 to 3  ×  1016 cm−3, respectively. These 2D images are the first application of TALIF imaging in moderate-pressure plasma discharges. 1D self-consistent modeling predictions show agreement with experimental results within the estimated experimental error of 25%. The present results can be used to further the development of higher fidelity kinetic models while quantifying plasma-source characteristics. [ABSTRACT FROM AUTHOR]

We describe a system designed to perform fixed-wavelength absorption spectroscopy of H2O vapor in practical combustion devices. The system includes seven wavelength-stabilized distributed feedback (WSDFB) lasers, each with a spectral accuracy of  ±1 MHz. An on-board external cavity diode laser (ECDL) that tunes 1320–1365 nm extends the capabilities of the system. Five system operation modes are described. In one mode, a sweep of the ECDL is used to monitor each WSDFB laser wavelength with an accuracy of  ±30 MHz. Demonstrations of fixed-wavelength thermometry at 10 kHz bandwidth in near-room-temperature gases are presented; one test reveals a temperature measurement error of ~0.43%. [ABSTRACT FROM AUTHOR]

Time-resolved particle image velocimetry (TR-PIV) has been achieved in a high-speed wind tunnel, providing velocity field movies of compressible turbulence events. The requirements of high-speed flows demand greater energy at faster pulse rates than possible with the TR-PIV systems developed for low-speed flows. This has been realized using a pulse-burst laser to obtain movies at up to 50 kHz, with higher speeds possible at the cost of spatial resolution. The constraints imposed by use of a pulse-burst laser are limited burst duration of 10.2 ms and a low duty cycle for data acquisition. Pulse-burst PIV has been demonstrated in a supersonic jet exhausting into a transonic crossflow and in transonic flow over a rectangular cavity. The velocity field sequences reveal the passage of turbulent structures and can be used to find velocity power spectra at every point in the field, providing spatial distributions of acoustic modes. The present work represents the first use of TR-PIV in a high-speed ground-test facility. [ABSTRACT FROM AUTHOR]

Femtosecond, two-photon-absorption laser-induced-fluorescence (fs-TALIF) spectroscopy is employed to measure space- and time-resolved atomic-oxygen distributions in a nanosecond, repetitively pulsed, externally grounded, atmospheric-pressure plasma jet flowing helium with a variable oxygen admixture. The high-peak-intensity, low-average-energy femtosecond pulses result in increased TALIF signal with reduced photolytic inferences. This allows 2D imaging of absolute atomic-oxygen number densities ranging from 5.8   ×   1015 to 2.0   ×   1012cm−3 using a cooled CCD with an external intensifier. Xenon is used for signal and imaging-system calibrations to quantify the atomic-oxygen fluorescence signal. Initial results highlight a transition in discharge morphology from annular to filamentary, corresponding with a change in plasma chemistry from ozone to atomic oxygen production, as the concentration of oxygen in the feed gas is changed at a fixed voltage-pulse-repetition rate. In this configuration, significant concentrations of reactive oxygen species may be remotely generated by sustaining an active discharge beyond the confines of the dielectric capillary, which may benefit applications that require large concentrations of reactive oxygen species such as material processing or biomedical devices. [ABSTRACT FROM AUTHOR]