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arXiv:physics/0105032 · Physical Review Letters

Observation of Coherent Transients in Ultrashort Chirped Excitation of an Undamped Two-Level System

Sébastien Zamith, J. Degert, Sabine Stock, B. de Beauvoir, Valérie Blanchet, M. A. Bouchène, B. Girard

Published Jun 28, 2001• 93 citations
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Abstract

The effects of coherent excitation of a two-level system with a linearly chirped pulse are studied theoretically and experimentally [in Rb (5s-5p)] in the low field regime. The coherent transients are measured directly on the excited state population on an ultrashort time scale. A sharp step corresponds to the passage through resonance. It is followed by oscillations resulting from interferences between off-resonant and resonant contributions. We finally show the equivalence between this experiment and Fresnel diffraction by a sharp edge.

DOI
10.1103/physrevlett.87.033001

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The effects of coherent excitation of a two-level system with a linearly chirped pulse are studied theoretically and experimentally [in Rb (5s-5p)] in the low field regime. The coherent transients are measured directly on the excited state population on an ultrashort time scale. A sharp step corresponds to the passage through resonance. It is followed by oscillations resulting from interferences between off-resonant and resonant contributions. We finally show the equivalence between this experiment and Fresnel diffraction by a sharp edge.
Excitation of a quantum ladder system by frequency-swept (-chirped) laser pulses has been investigated by studying an atomic model system, the 5s-5p-5d ladder of rubidium. The population transfer is significantly enhanced when the frequency is swept such that it follows the spacing of the ladder. At intermediate intensities we observe oscillations in the population transfer to the upper level (5d), which can be attributed to interference between two routes of excitation: sequential transfer and direct two-photon excitation via a virtual intermediate state. We determine simultaneously the population transfer to the upper level (5d) and the direct three-photon ionization, the latter corresponding to a three-step ladder with the final state being in the continuum: 5s-5p-5d-\ensuremath{\varepsilon}p/\ensuremath{\varepsilon}f. Experiments were performed, using 100 fs pulses at \ensuremath{\sim}780 nm from a self-mode-locked Ti:Al2{\mathrm{Al}}_{2}Al2​O3{\mathrm{O}}_{3}O3​ oscillator amplified at 10 Hz.
We will demonstrate that four-wave mixing with linearly chirped (phase-modulated) pulses is a unique tool for obtaining information on the dynamics and level structure of a system. Especially, it will be shown that the transient-grating-scattering type of experiment with chirped pulses provides an immediate answer to the question of whether the dynamics of a system occurs on a fast and/or slow time scale. In addition, we present compelling evidence that chirped four-wave mixing in a molecular system is a viable method for measuring excited-state vibrational frequencies. Double-sided Feynman diagrams are used for a third-order perturbative calculation of two-level four-wave-mixing effects and chirped coherent Raman scattering. The diagrams provide a visual representation of the quantum-mechanical pathways that the system can take as a result of the different field interactions. The number of quantum-mechanical pathways that contribute to the signal is shown to depend on the chirp rate compared to the time scale(s) of the system dynamics. A stochastic model is used to describe the optical dynamics of the system. The resulting expressions for the third-order nonlinear polarization are so complex that numerical calculations are necessary to simulate the time dependence of the optical response. It will also be shown that our theoretical results in the appropriate limits converge to those obtained for impulsive or continuous-wave excitation.
Computer simulations are presented to show that frequency-chirped ultrashort pulses, when properly employed, may be more effective than their compressed analogs for generating large-amplitude vibrational coherence in molecular systems. A one-dimensional model, which was used previously to simulate impulsive optical excitation of CsI, is used [ Chem. Phys. Lett.158, 238 ( 1988)]. A negatively chirped pulse (for which the light is red-shifted with time) is devised to excite the population initially onto the excited surface. As this population propagates in the repulsive upper state, the later red-shifted portions of the pulse follow the change in the resonance conditions and effectively dump the population back down into excited vibrational states of the ground surface. These results are compared with the dynamics simulated with the compressed and positively chirped analogs, and the experimental realization of this scheme is discussed.