Abstract
Quantitative femtosecond two-photon laser-induced fluorescence of atomic oxygen was demonstrated in an flame at pressures up to 10 atm. Femtosecond excitation at 226.1 nm was used to pump the electronic transition of atomic oxygen. Contributions from multiphoton de-excitation, production of atomic oxygen, and photolytic interferences were investigated and minimized by limiting the laser irradiance to . Quantitative agreement was achieved with the theoretical equilibrium mole fraction of atomic oxygen over a wide range of fuel–air ratios and pressures in an laminar calibration burner.
© 2019 Optical Society of America
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