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Physical Review A

Dark pulses for resonant two-photon transitions

P. Panek, Andreas Becker

Published Aug 23, 2006• 20 citations
Publisher

Abstract

We investigate the excitation of an atom or molecule via two-photon absorption induced by an ultrashort laser pulse in the perturbative intensity regime. We show that the probability for a resonant transition, i.e., with an intermediate state within the spectral width of the pulse, can be reduced to zero by pulses having a $\ensuremath{\theta}$-phase step at a certain detuning $\ensuremath{\delta}\ensuremath{\omega}$ from the central frequency. Our theoretical predictions are confirmed by numerical calculations for the $4s\ensuremath{\rightarrow}4d$ transition in the potassium atom.

DOI
10.1103/physreva.74.023408

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We investigate the excitation of an atom or molecule via two-photon absorption induced by an ultrashort laser pulse in the perturbative intensity regime. We show that the probability for a resonant transition, i.e., with an intermediate state within the spectral width of the pulse, can be reduced to zero by pulses having a \ensuremathθ\ensuremath{\theta}\ensuremathθ-phase step at a certain detuning \ensuremathδ\ensuremathω\ensuremath{\delta}\ensuremath{\omega}\ensuremathδ\ensuremathω from the central frequency. Our theoretical predictions are confirmed by numerical calculations for the 4s\ensuremath→4d4s\ensuremath{\rightarrow}4d4s\ensuremath→4d transition in the potassium atom.
Multiphoton transitions can be reached by many routes through a continuum of virtual levels. We show that the transition probability of two-photon and multiphoton processes can be controlled by tailoring the shape of an ultrashort excitation pulse, so that the many paths leading to the final state interfere to give a desired probability amplitude. We analyze the effect of pulse shapes on N-photon absorption as well as on Raman transitions. We show theoretically that certain tailored dark pulses do not excite the system at all, while other shaped pulses induce transitions as effectively as transform limited pulses, even when their peak amplitudes are greatly reduced. These results are confirmed experimentally for two-photon transitions in atomic cesium.
Two-photon absorption of a continuous train of ultrashort pulses in a gas gives rise to resonances when the sum of the frequencies of two locked modes coincides with the transition frequency in the gas. It is shown that the width of these resonances is not governed by the pulse duration but by the width of the twophoton transition. Resonance intensities are of the same order of magnitude as in the single-frequency regime at the same power level. It is worth noting an important feature of the use of ultrashort pulses in studies of two-photon resonances due to the 1S-2S transition in the hydrogen atom: there is a strong increase in the efficiency of conversion of dye laser radiation to the ultraviolet range.
An unconventional perturbation treatment of the theory of two-photon absorption in a four-level atomic system close to two-photon resonance is developed on the basis of the optical Bloch equations. The results for the longtime populations of the intermediate and upper states are valid in low- and medium-intensity regimes. In both regimes the upper state population shows a lorentzian resonance centred on zero two-photon detuning with a width equal to the natural linewidth of the upper state. The intermediate state population shows a similar behaviour in the intermediate regime only, with no significant dependence on two-photon detuning in the low-intensity regime. However, in both regimes the population of the virtual intermediate state is at least comparable to that of the resonant upper state. The perturbation theory results have been checked by direct numerical calculations based on the Bloch equations. Numerical calculations confirm the presence of a high-intensity regime characterized by power shifts, broadening and saturation effects.
We have considered the induced processes that occur in a driven two-level atom, where a laser photon is absorbed and emitted by the ground and by the excited states of the atom, respectively. In the low-intensity limit of the laser field, the induced spectra arising when a laser photon is absorbed by the ground state of the atom consist of two peaks describing induced-absorption and stimulated-emission processes, respectively, where the former prevails over the latter. Asymmetry of the spectral lines occurs at off-resonance and its extent depends on the detuning of the laser field. The physical, process where a laser photon is emitted by the excited state is the reverse of that arising from the absorption of a laser photon by the ground state of the atom. The former differs from the latter in that the emission of a laser photon by the excited state occurs in the low-frequency regime and that the stimulated-emission process prevails over that of the induced absorption. In this case, amplification of ultrashort pulses is likely to occur without the need of population inversion between the optical transitions. The computed spectra are graphically presented and discussed.
We describe optimized coherent control methods for two-photon transitions in atoms of a ladder-type three-state energy configuration. Our approach is based on the spatial coherent control scheme, which uses counterpropagating ultrashort laser pulses to produce complex excitation patterns in an extended space. Because coherent control requires constructive interference of constituent transition pathways, applying it to an atomic transition with a specific energy configuration requires specially designed laser pulses. We show in an experimental demonstration that two-photon transition with an intermediate resonant energy state can be coherently controlled and retrieved from the resonance-induced background, when phase flipping of the laser spectrum near the resonant intermediate transition is used. A simple reason for this behavior is the fact that the transition amplitude function (added to give an overall two-photon transition) changes its sign at the intermediate resonant frequency and, thus, by proper spectral-phase programing, the excitation patterns (or the position-dependent interference of the transition given as a consequence of the spatial coherent control) can be well isolated in space along the focal region of the counterpropagating pulses.
The relation between the spectral character of a completely off-resonant two-photon absorption and the non-impact collision dynamics of a three-level atomic system is studied. A collisionally induced resonance character in the spectral dependence of the absorption probability is shown theoretically. Measured results about the dependence of fluorescence intensity on the incident light frequencies are ingood agreement with the theory. The interatomic potential between the sodium 4D state and argon is also estimated from experimental results.