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New Journal of Physics

Pulsed cooperative backward emissions from non-degenerate atomic transitions in sodium

Jonathan V. Thompson, Charles W. Ballmann, Han Cai, Zhenhuan Yi, Yuri V. Rostovtsev, Alexei V. Sokolov, Philip Hemmer, Aleksei M. Zheltikov, Gombojav O. Ariunbold, Marlan O. Scully

Published Oct 9, 2014• 20 citations
Publisher

Abstract

We study backward cooperative emissions from a dense sodium atomic vapor. Ultrashort pulses produced from a conventional amplified femtosecond laser system with an optical parametric amplifier are used to excite sodium atoms resonantly on the two-photon 3S –4S transition. Backward superfluorescent emissions (BSFEs), both on the 4S –3P and 4S –3P transitions, are observed. The picosecond temporal characteristics of the BSFE are observed using an ultrafast streak camera. The power laws for the dependencies of the average time delay and the intensity of the BSFEs on input power are analyzed in the sense of cooperative emission from nonidentical atomic species. As a result, an absolute (rather than relative) time delay and its fluctuations (free of any possible external noise) are determined experimentally. The possibility of a backward swept-gain superfluorescence as an artificial laser guide star in the sodium layer in the mesosphere is also discussed.

DOI
10.1088/1367-2630/16/10/103017

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We study backward cooperative emissions from a dense sodium atomic vapor. Ultrashort pulses produced from a conventional amplified femtosecond laser system with an optical parametric amplifier are used to excite sodium atoms resonantly on the two-photon 3S –4S transition. Backward superfluorescent emissions (BSFEs), both on the 4S –3P and 4S –3P transitions, are observed. The picosecond temporal characteristics of the BSFE are observed using an ultrafast streak camera. The power laws for the dependencies of the average time delay and the intensity of the BSFEs on input power are analyzed in the sense of cooperative emission from nonidentical atomic species. As a result, an absolute (rather than relative) time delay and its fluctuations (free of any possible external noise) are determined experimentally. The possibility of a backward swept-gain superfluorescence as an artificial laser guide star in the sodium layer in the mesosphere is also discussed.
We study infrared backward cooperative emission in a rubidium vapor induced by ultrafast two-photon optical excitations. The laser coherent control of the backward emission is demonstrated by using a pair of 100 fs pulses with a variable time delay. The temporal variation (quantum beat) of the backward beam intensity due to interference of atomic transitions in the rubidium atomic level system 5S-5P-5D is produced and controlled. Based on the obtained experimental results, we discuss possible applications of the developed approach for creation of an effective “guide star” in the sodium atomic layer in the upper atmosphere (mesosphere).
We study the superfluorescence (SF) from a gas of rubidium atoms. The atoms of a dense vapor are excited to the 5D5D5D state from the 5S5S5S state by a two-photon process driven by 100-fs laser pulses. The atoms decay to the 6P6P6P state and then to the 5S5S5S state. The SF emission at 420 nm on the 6P6P6P--5S5S5S transition is recorded by a streak camera with picosecond time resolution. The time duration of the generated SF is tens of picoseconds, which is much shorter than the time scale of the usual relaxation processes, including spontaneous emission and atomic coherence dephasing. The dependence of the time delay between the reference input pulse and SF is measured as a function of laser power. The experimental data are described quantitatively by a simulation based on the semiclassical atom-field interaction theory. The observed change in scaling laws for the peak intensity and delay time can be elucidated by an SF theory in which the sample length is larger than the cooperation length.
Technological progress in commercializing ultrafast lasers and detectors has allowed realization of cooperative processes on an ultrashort time scale, which demand a re-evaluation of the conventional cooperative phenomena with a new insight. Ultrafast cooperative phenomena in coherently prepared media and various applications of superfluorescence and coherent Raman scattering are studied in this dissertation. In particular, a simple theoretical testimony on analogy between a cooperative emission and coherent Raman scattering is presented by offering an opportunity to perform parallel research on these two processes from a unified point of view.\n\nOn one hand, the superfluorescent pulse with a time duration of a few tens of picoseconds (ps) from alkali metal vapor is observed for the first time, even though cooperative phenomena in atomic vapor have been extensively studied for more than five decades. A dense rubidium vapor pumped by ultrashort (100 femtosecond, fs) pulses allows a realization of the ultrafast superfluorescence while a time-resolved study of superfluorescence is accomplished by using a streak camera with 2 ps time resolution. Experimental research on quantum nature of cooperative emissions has been “frozen” over the years (three decades) possibly because of the technical difficulties. Quantum fluctuations of superfluorescence development are explored experimentally by taking advantage of the ultra fast streak camera. Presumable applications of the superfluorescent pulse in e.g., a remote sensing, and an ultraviolet upconversion of the input infrared laser pulse are presented. The quantum interference due to different excitation pathways is revealed by the temporal coherent control technique while observing interferometric signals from alkali metal vapors. \n\nOn the other hand, a new spectroscopic technique based on ultrafast coherent Raman scattering is developed. The key advantage of the presented technique is to suppress the non-resonant background noise which usually obscures possible applications of the other conventional coherent Raman techniques in practice. A reduction of the background noise is achieved by shaping and delaying the third pulse which probes the coherence of the medium (i.e., an enhancement of specific vibrations of the target molecules in unison) firstly prepared by two broadband pulses. We demonstrate a robustness and superiority of signal-to-noise ratio of the developed technique by identifying as few as 10000 bacterial spores at a single laser shot level.\n\nFinally, several comparative studies between cooperative and uncooperative processes are presented. A picosecond cooperative phenomenon in a three-photon resonant medium induced by a single as well as two-color ultrashort pulses is investigated. A time-resolved study shows that a picosecond cooperative effect is crucial in the well-established fields of resonant-enhanced multiphoton ionizations and harmonic generations. We also present a quantitative analysis for spontaneous versus broadband coherent Raman scattering on pyridine molecules. The spontaneous Raman signal is enhanced by 5 orders as a result of cooperative phenomena.
levels of atomic sodium using ultrashort laser pulses in a stepwise excitation scheme. Two broadband femtosecond laser pulses are used to excite the 6S level from the 3S ground level in sodium vapor. The first one is simultaneously resonant with the D1 and D2 lines of the 3S→3P transition, and the second one with the 3P→6S transition. The delay between the two pulses is scanned in order to probe the dephasing between the two excited intermediate levels. Quantum beating is observed by monitoring the fluorescence signals at 330 nm and 515 nm, namely transition 4P→3S and 6S→3P, respectively. Signals are compared to a semi-classical model that reproduces the oscillations with a very good agreement.
We report second-order intensity correlations g ( 2 ) ( τ ) of directional midinfrared emissions from sodium vapor under bichromatic continuous-wave excitation. Directional emission at 2.34 µ m in the forward direction and at 2.21 µ m in both forward and backward directions exhibits g ( 2 ) ( 0 ) values that exceed unity yet remain well below the thermal limit of 2, indicating subthermal photon bunching characteristics of a multimode collectively driven process rather than purely independent amplified spontaneous emission. Cross-correlation measurements reveal that the counterpropagating 2.21 − µ m beams are positively correlated, demonstrating dynamic coupling between the two emission channels. Persistent oscillations in g ( 2 ) ( τ ) , observed across a broad range of pump powers, shift systematically to higher frequencies with increasing excitation power, consistent with ac Stark shifts of hyperfine sublevels. Together, these observations establish that the emission arises from a phase-matched, continuous-wave collective process combining features of mirrorless lasing and amplified spontaneous emission, with long-range dipole coherence and velocity-selective coupling governing the photon statistics and the forward-backward emission symmetry. The experiment uses a 10-cm buffer-gas-free sodium vapor cell under bichromatic excitation at 589.2 and 569.0 nm; the emitted midinfrared light is detected in a Hanbury Brown–Twiss configuration. The demonstrated backward emission is of particular interest for applications in laser guide star generation and mesospheric remote sensing, where understanding the statistical properties of the emitted light is essential for optimizing sodium-based light sources.
We investigate picosecond cooperative emission in an ensemble of rubidium atoms coherently excited by 100-fs laser pulses that are three-photon resonant to the 6P6P6P-5S5S5S transition. The emitted 420-nm light is recorded by a streak camera with 2-ps resolution. The resultant pulse shape shows ringing typical for superradiance in extended sample. The pulse shape is measured as a function of input power and is compared to the solutions of Maxwell-Bloch equations. The observed superradiance, which is in the low-excitation regime, is found to be closely related to optical precursor behavior.