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Bidirectional Flame Lasing

Pengji Ding, Maria Ruchkina, Marcus Aldén, Joakim Bood

Published Jan 1, 2018• 0 citations

Abstract

Lasing refers to the generation of highly directional laser-like emission remotely pumped by laser pulses in a medium such as ambient air or a flame.It has been intensively investigated because of its potentials to revolutionize the field of remote sensing.Earlier studies were carried out in flames, where lasing effect has been observed in various radicals, for example H, O, N etc., through two-photon resonant excitation.This scheme was later applied to generate lasing of O and N in ambient air, which can be dramatically improved by predissociation of the air constituents.However, the underlying physical mechanism of two-photon-excited lasing effect is still unsettled although it has been studied for more than one decade.Currently there are three different proposals: (1) Amplified Spontaneous Emission (ASE), in which case population inversion is responsible for optical gain;(2) Superfluorescence (SF), where a macroscopic dipole occurs in the population inverted medium; (3) Both hyper-Raman scattering and four-wave mixing are involved in the generation of lasing emission.Here, we experimentally studied 656 nm lasing emission of atomic hydrogen via two-photon resonant excitation by focusing 125-fs laser pulses of 205-nm wavelength in a methane/oxygen welding flame (see Fig. 1), where hydrogen atoms are naturally present.Lasing occurs in both forward and backward directions, and the forward signal strength is almost one order of magnitude stronger than the backward one.It has been found that the durations of lasing pulses are around 20 ps, and decreases with increasing pump laser energies.Furthermore, the delay of the lasing pulse with respect to the pump pulse decreases with increasing pump energies.These results show high similarities with the behaviors of SF, suggesting that the femtosecond two-photonexcited lasing emission of atomic hydrogen might be SF.

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Among different approaches to generate mirrorless lasing, resonant multiphoton pumping of gas constituents by deep-UV laser pulses exhibits so far the highest efficiency and produces measurable lasing energies, but the underlying mechanism was not yet fully settled. Here, we report lasing generation from atomic oxygen in a methane-air flame via femtosecond two-photon excitation. Temporal profiles of the lasing pulses were measured for varying concentrations of atomic oxygen, which shows that the peak intensity and time delay of the lasing pulse approximately scales as $N$ and $1/\sqrt{N}$, respectively, where $N$ represents the concentration. These scaling laws match well with the prediction of oscillatory superfluorescence (SF), indicating that the lasing we observed is essentially SF rather than amplified spontaneous emission. In addition, the quantum-beating effect was also observed in the time-resolved lasing pulse. A theoretical simulation based on nonadiabatic Maxwell-Bloch equations well reproduces the experimental observations of the temporal dynamics of the lasing pulses. These results on fundamentals should be beneficial for the better design and applications of lasing-based techniques.

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Air lasing induced by laser filamentation opens a new route for research on atmospheric molecular physics and remote sensing. The generation of air lasing is composed of two processes, i.e., building up optical gain of air molecules in femtosecond time scale and emitting coherent radiation in picosecond time scale. Here, we focus on the emission mechanisms of N 2 + air lasing and reveal, by examining the intensities and temporal profiles of N 2 + lasing at 391 nm generated respectively in a time-varying polarization-modulated and a linearly polarized pump laser field under different nitrogen gas pressures, that the N 2 + lasing can emit through either triggered super-radiance or seed amplification. We find that the two pressure-sensitive factors, i.e., the dipole dephasing time T 2 and the population inversion density n , determine which of these two mechanisms dominates the N 2 + lasing emission process, enabling manipulation of the transition from triggered super-radiance to seed amplification or vice versa. Our findings clarify the emission mechanism of N 2 + lasing under different pressures and provide a deeper understanding of N 2 + air lasing not only in the establishment of optical gain but also in the lasing emission process.

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Lasing refers to the generation of highly directional laser-like emission remotely pumped by laser pulses in a medium such as ambient air or a flame.It has been intensively investigated because of its potentials to revolutionize the field of remote sensing.Earlier studies were carried out in flames, where lasing effect has been observed in various radicals, for example H, O, N etc., through two-photon resonant excitation.This scheme was later applied to generate lasing of O and N in ambient air, which can be dramatically improved by predissociation of the air constituents.However, the underlying physical mechanism of two-photon-excited lasing effect is still unsettled although it has been studied for more than one decade.Currently there are three different proposals: (1) Amplified Spontaneous Emission (ASE), in which case population inversion is responsible for optical gain;(2) Superfluorescence (SF), where a macroscopic dipole occurs in the population inverted medium; (3) Both hyper-Raman scattering and four-wave mixing are involved in the generation of lasing emission.Here, we experimentally studied 656 nm lasing emission of atomic hydrogen via two-photon resonant excitation by focusing 125-fs laser pulses of 205-nm wavelength in a methane/oxygen welding flame (see Fig. 1), where hydrogen atoms are naturally present.Lasing occurs in both forward and backward directions, and the forward signal strength is almost one order of magnitude stronger than the backward one.It has been found that the durations of lasing pulses are around 20 ps, and decreases with increasing pump laser energies.Furthermore, the delay of the lasing pulse with respect to the pump pulse decreases with increasing pump energies.These results show high similarities with the behaviors of SF, suggesting that the femtosecond two-photonexcited lasing emission of atomic hydrogen might be SF.

Among different approaches to generate mirrorless lasing, resonant multiphoton pumping of gas constituents by deep-UV laser pulses exhibits so far the highest efficiency and produces measurable lasing energies, but the underlying mechanism was not yet fully settled. Here, we report lasing generation from atomic oxygen in a methane-air flame via femtosecond two-photon excitation. Temporal profiles of the lasing pulses were measured for varying concentrations of atomic oxygen, which shows that the peak intensity and time delay of the lasing pulse approximately scales as

N

and

1/\sqrt{N}

, respectively, where

N

represents the concentration. These scaling laws match well with the prediction of oscillatory superfluorescence (SF), indicating that the lasing we observed is essentially SF rather than amplified spontaneous emission. In addition, the quantum-beating effect was also observed in the time-resolved lasing pulse. A theoretical simulation based on nonadiabatic Maxwell-Bloch equations well reproduces the experimental observations of the temporal dynamics of the lasing pulses. These results on fundamentals should be beneficial for the better design and applications of lasing-based techniques.

We investigate the excited-state dynamics of hydrogen (H) atoms in flames by using a femtosecond (fs) pump-probe scheme and measuring directional emission signals. An approximately 100-fs pump pulse at 205.1 nm excites H atoms through a two-photon process (n = 3 ←← n = 1), which is followed by detection of the forward emission signals induced by a broadband fs probe pulse near 656 nm. Above a certain threshold, we observe a quadratic dependence of the emission signal on the pump laser energy. Moreover, the linewidth of the forward emission signal varies with the probe delay and the probe laser energy. This behavior can be explained in terms of superradiance. We perform a theoretical analysis and compare the experimental results with the theory, and conclude that, within the conditions of our experiment, the behavior of the atomic system involves atomic coherence, which is produced non-adiabatically and corresponds to a superradiant process. Variations in the duration of the gain time window and lifetime of the excited-state H atoms in flames are explored at different flame conditions (i.e., equivalence ratio and heights above the burner). The fs pump-probe technique demonstrated here can also be extended to characterize the time-resolved population dynamics and the corresponding collisional energy transfer rates for energy levels involved in laser-induced fluorescence detection of H atoms in flames relevant to practical combustion applications.

Air lasing is a concept that refers to remote no-cavity (mirrorless) optical amplification in ambient air with the air constituents as the gain media. Due to the high potential of air lasing in view of applications in atmospheric sensing, a variety of pumping schemes have been proposed so far for building up population-inverted gain media in air and producing forward and/or backward directional lasing emissions. This review paper presents an overview of recent advances in the experimental observations and physical understanding of air lasing in various pumping schemes of air molecules by intense laser fields. Special emphasis is given to the strong-field-induced N 2 + air lasing, the mechanism of which is currently still in a hot debate.

Strong excitation with high electromagnetic fields can generate lasing in gaseous media by resonant excitation. Previous efforts have shown that the lasing signal can be emitted perpendicular to the direction of the pump laser if the shape of the gain volume can be controlled. This paper reports on the characterization of sideways emitted lasing obtained through two-photon pumping in oxygen atoms present in a flame. Intense 35-fs laser pulses of 226-nm wavelength focused into a sheet by a cylindrical mirror are used to form a gain volume geometry that yields an 845-nm lasing beam that is emitted perpendicular to the pump-beam direction. The sideways lasing has been investigated in terms of its pump laser energy dependence, excitation and emission spectra, and spatial characteristics. Single-shot images of the emission exhibit interference fringes, revealing that the emission contains multiple coherent spatial modes. The results indicate that superfluorescence constitutes a significant contribution to the sideways lasing. We believe that this is the first important step for understanding and using sideways lasing as a phenomenon and tool for future applications and inventions.

Cavity-free lasing in atmospheric air has stimulated intense research toward a fundamental understanding of underlying physical mechanisms. In this Letter, we identify a new mechanism-a third-harmonic photon mediated resonant energy transfer pathway leading to population inversion in argon via an initial three-photon excitation of nitrogen molecules irradiated by intense 261 nm pulses-that enables bidirectional two-color cascaded lasing in atmospheric air. By making pump-probe measurements, we conclusively show that such cascaded lasing results from superfluorescence rather than amplified spontaneous emission. Such cascaded lasing with the capability of producing bidirectional multicolor coherent pulses opens additional possibilities for remote sensing applications.

Air lasing induced by laser filamentation opens a new route for research on atmospheric molecular physics and remote sensing. The generation of air lasing is composed of two processes, i.e., building up optical gain of air molecules in femtosecond time scale and emitting coherent radiation in picosecond time scale. Here, we focus on the emission mechanisms of N 2 + air lasing and reveal, by examining the intensities and temporal profiles of N 2 + lasing at 391 nm generated respectively in a time-varying polarization-modulated and a linearly polarized pump laser field under different nitrogen gas pressures, that the N 2 + lasing can emit through either triggered super-radiance or seed amplification. We find that the two pressure-sensitive factors, i.e., the dipole dephasing time T 2 and the population inversion density n , determine which of these two mechanisms dominates the N 2 + lasing emission process, enabling manipulation of the transition from triggered super-radiance to seed amplification or vice versa. Our findings clarify the emission mechanism of N 2 + lasing under different pressures and provide a deeper understanding of N 2 + air lasing not only in the establishment of optical gain but also in the lasing emission process.