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Journal of the Optical Society of America B

Coherent propagation effect of incoherent light

Norio Morita, Kenji Torizuka, Tatsuo Yajima

Published Apr 1, 1986• 17 citations
Publisher

Abstract

The coherent propagation phenomenon of incoherent light through a resonant medium was experimentally demonstrated in the subpicosecond time region, using Na atoms and the light from an imperfectly mode-locked cw dye laser. The coherence spike with a 0.35-psec width in the cross-correlation profile between the propagated incoherent light and the initial light develops the same specific oscillatory structure as seen in the propagation of a weak coherent subpicosecond pulse. A theoretical analysis was also performed, and the experimental results are in considerably good agreement with the calculated ones.

DOI
10.1364/josab.3.000548

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The coherent propagation phenomenon of incoherent light through a resonant medium was experimentally demonstrated in the subpicosecond time region, using Na atoms and the light from an imperfectly mode-locked cw dye laser. The coherence spike with a 0.35-psec width in the cross-correlation profile between the propagated incoherent light and the initial light develops the same specific oscillatory structure as seen in the propagation of a weak coherent subpicosecond pulse. A theoretical analysis was also performed, and the experimental results are in considerably good agreement with the calculated ones.
Coherent excitation of an atomic excited state occurs during the propagation of near-resonant light pulses and is responsible for the induced polarization. Simultaneously, incoherent excitation occurs due to the relaxation processes described by the absorption coefficient. Here, the theory for the coherent and incoherent excitation is initially presented in terms of the traditional vector model. While a complete understanding of the two-level system is provided by the vector model, it is shown to be incomplete when the problem of directly monitoring the coherent and incoherent excitation is considered. This is because this latter problem involves more than two levels. For this more complicated multilevel problem, adiabatic states are introduced to gain further understanding. The adiabatic states are the stationary states of the atom in the presence of the near-resonant laser field; they help to explain the intimate connection between the coherent excitation and the two-photon resonance. Experimental measurements of the coherent and incoherent excitation associated with near-resonant pulse propagation in Rb vapor are presented. The double-resonance technique used a relatively strong pulsed dye laser tuned near the $5{S}_{\frac{1}{2}}\ensuremath{\leftrightarrow}5{P}_{\frac{1}{2}}$ transition (7948 \AA{}A) of Rb to produce the coherent and incoherent excitation, and a weak, tunable cw dye laser tuned in the region of the $5{P}_{\frac{1}{2}}\ensuremath{\leftrightarrow}6{D}_{\frac{3}{2}}$ transition (6206 \AA{}A) to monitor this excitation. In agreement with theory, the experimental results demonstrate that coherent excitation is responsible for two-photon absorption, while the incoherent excitation corresponds to one-photon absorption to the 5P125{P}_{\frac{1}{2}}5P21​​ state.
The pulse distortion in GaAs quantum wells was studied by means of a light-gating technique. In the experiment, we used the incoherent picosecond pulse to observe accurately the changes of the coherent spike and its surrounding envelope. The experimental results clearly showed that the pulse is not anomalously delayed but is strongly distorted around the exciton resonance. We also compared the results with a computational simulation based on the absorption saturation mechanism. The simulated results agreed well with experimental results. The simulation showed that the recovery time of the exciton saturation is 90 ps around the tail part of the exciton absorption. We also observed a reduction of the coherent spike around the exciton resonance. Theoretical calculations indicate that the coherent-propagation effect in the linear absorber causes the reduction of the coherent spike.
An ultrashort weak pulse that propagates resonantly on the $\ensuremath{\mid}a⟩\ensuremath{\rightarrow}\ensuremath{\mid}b⟩$ transition of a three-level system $(\ensuremath{\mid}a⟩,\ensuremath{\mid}b⟩,\ensuremath{\mid}c⟩)$ experiences reshaping effects on a time scale longer than its duration. When a strong field is applied (nonresonantly) on the $\ensuremath{\mid}b⟩\ensuremath{\rightarrow}\ensuremath{\mid}c⟩$ transition, important light shifts are induced. We have theoretically studied the novel behavior of both the medium and weak propagating laser pulses in such conditions. For the transmitted field profile, drastic changes occur: at long times, efficient reduction of the distortion is obtained, while strong oscillations appear for short times, mapping out the dynamical light shift. These shaping effects, which are accompanied by new features in the spectrum for the propagating pulse, are interpreted as the result of the interference between incident field and induced dipole radiated field, whose frequency sweeps in time because of the induced light shift.
A new method to measure picosecond or subpicosecond vibrational-dephasing dynamics with the use of incoherent or broadband light is presented theoretically and experimentally. It is based on a transient coherent Raman process with three beams. In our experimental scheme, two of them are incoherent light from a single source, and a delay time between the two is variable. A third beam has a higher frequency than the incoherent light by a vibrational energy in a molecule of interest, and is coherent in the delay-time range of the measurement. The delay-time dependence of coherent Stokes Raman scattering (CSRS) intensity offers the information about the coherence dynamics of the vibrational transition with a resolution time determined only by the correlation time of the incoherent light. For the theoretical calculation, a three-level model of the molecular system with homogeneous broadening is used, and delay-time dependences of the CSRS signal are calculated for off-resonance and resonance cases. Dephasing dynamics of the 2915-${\mathrm{cm}}^{\mathrm{\ensuremath{-}}1}$ mode in dimethylsulfoxide was observed experimentally by the new method with the use of nanosecond laser pulses, and the result agrees well with that obtained with picosecond pulses.
The nonstationary pump-probe interaction between short laser pulses propagating in a resonant optically dense coherent medium is considered. Special attention is paid to the case where the density of two-level particles is high enough that a considerable part of the energy of relatively weak external laser fields can be coherently absorbed and reemitted by the medium. Thus, the field of the medium reaction plays a key role in the interaction processes, which leads to collective behavior of an atomic ensemble in the strongly coupled light-matter system. Such behavior results in fast excitation interchanges between the field and a medium in the form of optical ringing, which is analogous to polariton beating in solid-state optics. This collective oscillating response, which can be treated as successive beats between light wave packets of different group velocities, is shown to significantly affect the propagation and amplification of the probe field under its nonlinear interaction with a nearly copropagating pump pulse. Depending on the probe-pump time delay, the probe transmission spectra show the appearance of either a specific doublet or coherent dip. The widths of these features are determined by the density-dependent field-matter coupling coefficient and increase during the propagation. Besides that, the widths of the coherent features, which appear close to resonance in the broadband probe spectrum, exceed the absorption-line width, since under the strong-coupling regime, the frequency of optical ringing exceeds the rate of incoherent relaxation. Contrary to stationary strong-field effects, the density- and coordinate-dependent transmission spectra of the probe manifest the importance of collective oscillations and cannot be obtained in the framework of a single-atom model.