RESUMEN
A method based on femtosecond two-photon excitation has been developed for simultaneous visualization of interference-free fluorescence of H and O atoms in turbulent flames. This work shows pioneering results on single-shot simultaneous imaging of these radicals under non-stationary flame conditions. The fluorescence signal, showing the distribution of H and O radicals in premixed CH4/O2 flames was investigated for equivalence ratios ranging from Ï = 0.8 to Ï = 1.3. The images have been quantified through calibration measurements and indicate single-shot detection limits on the order of a few percent. Experimental profiles have also been compared with profiles from flame simulations, showing similar trends.
RESUMEN
We present a novel method, to our knowledge, to control the shape of the spectra using 2-beam hybrid femtosecond (fs)/nanosecond (ns) coherent anti-Stokes Raman scattering (RCARS). The method is demonstrated experimentally and theoretically by utilizing a species-selective excitation approach via a field-free molecular alignment as an illustrative example. Two non-resonant fs laser pulses with proper delay selectively create and then annihilate N2 resonances in a binary mixture with O2 molecules. The RCARS signal is simultaneously resolved in spectral and temporal domains within a single-shot acquisition. The method requires very low pulse energies for excitation, hence minimizing multiphoton ionization probability, allowing for coherent control at various temperatures and pressures, with spectroscopic applications in non-stationary and unpredictable reacting flows.
RESUMEN
Laser-induced grating spectroscopy (LIGS) is for the first time explored in a configuration based on the crossing of two focused femtosecond (fs) laser pulses (800-nm wavelength) and a focused continuous-wave (cw) laser beam (532-nm wavelength). A thermal grating was formed by multi-photon absorption of the fs-laser pulses by [Formula: see text] with a pulse energy around 700 [Formula: see text]J ([Formula: see text] 45 TW/[Formula: see text]). The feasibility of this LIGS configuration was investigated for thermometry in heated nitrogen gas flows. The temperature was varied from room temperature up to 750 K, producing strong single-shot LIGS signals. A model based on the solution of the linearized hydrodynamic equations was used to extract temperature information from single-shot experimental data, and the results show excellent agreement with the thermocouple measurements. Furthermore, the fluorescence produced by the fs-laser pulses was investigated. This study indicates an 8-photon absorption pathway for [Formula: see text] in order to reach the [Formula: see text] state from the ground state, and 8 + 5 photon excitation to reach the [Formula: see text] state of the [Formula: see text] ion. At pulse energies higher than 1 mJ, the LIGS signal was disturbed due to the generation of plasma. Additionally, measurements in argon gas and air were performed, where the LIGS signal for argon shows lower intensity compared to air and [Formula: see text].
RESUMEN
In this Letter, we have investigated 845 nm lasing generation in atomic oxygen, present in a lean methane-air flame, using two-photon pumping with femtosecond 226 nm laser pulses, particularly focusing on the impact of nanosecond repetitively pulsed glow discharges forcing on the backward lasing signal. Characterizations of the backward lasing pulse, in terms of its spectrum, beam profile, pump pulse energy dependence, and divergence, were conducted to establish the presence of lasing. With plasma forcing of the flame, the backward lasing signal was observed to be enhanced significantly, â¼50%. The vertical concentration profile of atomic oxygen was revealed by measuring the backward lasing signal strength as a function of height in the flame. The results are qualitatively consistent with results obtained with two-dimensional femtosecond two-photon-absorption laser-induced fluorescence, suggesting that the backward lasing technique can be a useful tool for studies of plasma-assisted combustion processes, particularly in geometries requiring single-ended standoff detection.
RESUMEN
A model based on rate-equation analysis has been developed for simulation of two-photon-excited laser-induced fluorescence of carbon monoxide (CO) in the Hopfield-Birge band at 230â nm. The model has been compared with experimental fluorescence profiles measured along focused beams provided by lasers emitting nano-, pico-, and femtosecond pulses. Good quantitative agreement was obtained between simulations and experimental data obtained in premixed CH4/C2H4-air flames. For excitation with femtosecond pulses, experimental and simulated fluorescence signals showed quadratic dependence on laser power under conditions of low laser irradiance, whereas different sublinear dependencies were obtained at higher irradiances due to photoionization. Simulations of CO signal versus femtosecond laser linewidth suggest the strongest signal for a transform-limited pulse, which is sufficiently broad spectrally to cover the CO Q-branch absorption spectrum. Altogether, the developed rate-equation model allows for analysis of two-photon excitation fluorescence to arrange suitable diagnostic configurations and retrieve quantitative data for CO as well as other species in combustion, such as atomic oxygen and hydrogen.
RESUMEN
By aiming to establish single-ended standoff combustion diagnostics, bidirectional lasing emissions of atomic hydrogen at 656 nm wavelength have been generated via two-photon resonant excitation by focusing 205 nm femtosecond laser pulses into a premixed CH4/O2 flame. The forward lasing strength is approximately one order of magnitude stronger than that of the backward one, due to the geometry of traveling wave excitation over a 2-mm-long pencil-shaped gain volume and the short gain lifetime of 3.5 ps. The gain coefficient of hydrogen lasing was determined to approximate 52/cm. As for the underlying physics of hydrogen lasing, amplified spontaneous emission (ASE) occurs simultaneously with four-wave mixing (FWM), and ASE dominates in the forward direction, whereas the backward lasing is virtually only ASE.
RESUMEN
We report on an observation of bi-directional 656 nm lasing action of atomic hydrogen in a premixed CH4/air flame induced by resonant femtosecond 205 nm two-photon excitation. In particular, the backward-propagating lasing pulse is characterized in the spatial and temporal domains for the sake of a single-ended diagnostic. Its picosecond-scale duration and smooth temporal profile enable spatially resolved detection of hydrogen atoms in the millimeter range, which is successfully demonstrated using two narrow welding flames.