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Physical Review Research

All-optical Stückelberg spectroscopy of strongly driven Rydberg states

Ulrich Bengs, Serguei Patchkovskii, Misha Ivanov, Nickolai Zhavoronkov

Published May 19, 2022• 10 citations
Publisher

Abstract

The AC Stark shift of electronic levels is ubiquitous in the interaction of intense light fields with atoms and molecules. As the light intensity changes on the rising and falling edges of a femtosecond laser pulse, it shifts the Rydberg states in and out of multiphoton resonances with the ground state. The two resonant pathways for transient excitation arising at the leading and the trailing edges of the pulse generate Young's type interference, generally referred to as the St\"uckelberg oscillations. Here we report the observation of the St\"uckelberg oscillations in the intensity of the coherent free-induction decay following resonant multiphoton excitation. Moreover, combining the experimental results with accurate numerical simulations and a simple model, we use the St\"uckelberg oscillations to recover the population dynamics of strongly driven Rydberg states inside the laser pulse by all-optical measurements after the end of the pulse. We demonstrate the potential of this spectroscopy to characterize lifetimes of Rydberg states dressed by laser fields with strengths far exceeding the Coulomb field between the Rydberg electron and the core.

DOI
10.1103/physrevresearch.4.023135

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The AC Stark shift of electronic levels is ubiquitous in the interaction of intense light fields with atoms and molecules. As the light intensity changes on the rising and falling edges of a femtosecond laser pulse, it shifts the Rydberg states in and out of multiphoton resonances with the ground state. The two resonant pathways for transient excitation arising at the leading and the trailing edges of the pulse generate Young's type interference, generally referred to as the St"uckelberg oscillations. Here we report the observation of the St"uckelberg oscillations in the intensity of the coherent free-induction decay following resonant multiphoton excitation. Moreover, combining the experimental results with accurate numerical simulations and a simple model, we use the St"uckelberg oscillations to recover the population dynamics of strongly driven Rydberg states inside the laser pulse by all-optical measurements after the end of the pulse. We demonstrate the potential of this spectroscopy to characterize lifetimes of Rydberg states dressed by laser fields with strengths far exceeding the Coulomb field between the Rydberg electron and the core.
We conduct a systematic investigation of the oscillations of the Rydberg-state populations as a function of intensity arising from strong-field multiphoton excitation of Rydberg atoms. By numerically solving the time-dependent Schrödinger equation and by constructing a quantum model based on Freeman resonances, we elucidate the underlying physical mechanisms governing the intensity-dependent oscillatory behavior of the Rydberg-state population dynamics. Our analysis shows that these oscillations originate from the synergistic interplay of three distinct quantum-interference mechanisms: (1) interference between excitation pathways at the rising and falling edges of the laser pulse (long-time interference), (2) interference between different optical cycles within the same side of the laser pulse (short-time interference), and (3) interference within individual optical cycles (intracycle interference). Additionally, we find that ground-state depletion has varying degrees of influence on the oscillation patterns formed by the three interference mechanisms under different laser-intensity conditions.
Abstract We demonstrate how strong-field multiphoton transitions between dynamically shifted atomic levels can be traced in the energy spectra of emitted photoelectrons. Applying an ultrafast and intense laser pulse, two-photon Rabi oscillations are induced between two bound states of an atom. A third photon from the same pulse directly ionizes the atom, thus the emitted photoelectrons coherently probe the underlying dynamics. As the instantaneous energy of photoelectrons follows the pulse intensity envelope, modulated by the ac Stark shifts, electrons emitted with the same energy but at different times—at the rising and falling edge of the pulse—will interfere leading to pronounced dynamic interference pattern in the spectra. We investigate this phenomenon both numerically and analytically by developing a minimal three-state model that incorporates two-photon coupling and dynamically shifted atomic levels. On the example of atomic lithium (2 s → → 4 s → continuum) we show how the individual ac Stark shifts and the two-photon Rabi frequency are reflected through the asymmetry, shifting and splitting of the interference structure of the computed photopeaks.
The coherent control of atomic energy level population is important for several areas physics and engineering including fluorescent spectroscopy, resonantly enhanced multiphoton ionization, harmonic generation, remote sensing and lasing. At low intensities where the Stark shift can be neglected, coherent control mechanisms usually exploit resonances created from stationary energy states dressed by integer multiples of the photon energy. However, in the strong field limit where large laser pulse intensities lead to significant Stark shifts, the resonant conditions are dynamic both in time and space and will likely not be satisfied for the entire laser pulse or beam.\n\nIn this research, we experimentally and theoretically demonstrate coherent control of atomic energy level population in sodium vapor as well as the selective excitation of sodium Rydberg levels using high intensity laser pulses. We also make a direct measurement of the ponderomotive shift of the continuum. While techniques based on resonance interferences and rapid adiabatic passage have been introduced for selective excitation, the conditions that must be satisfied for these phenomena can be hampered by short femtosecond pulse durations and large Stark shifts. In contrast, a technique referred to here as Resonance Sampling, uses the AC Stark shifts to selectively induce Freeman resonances and is resilient to changes in the spectral phase. Freeman resonances established in this way can result in population inversion of the excited state, and may lead to new lasing mediums and remote sensing applications.\n\n\nIn this research, we experimentally and theoretically demonstrate coherent control of atomic energy level population in sodium vapor as well as the selective excitation of sodium Rydberg levels using high intensity laser pulses. While techniques based on resonance interferences and rapid adiabatic passage have been introduced for selective excitation, the conditions that must be satisfied for these phenomena can be hampered by short femtosecond pulse durations and large Stark shifts. In contrast, a technique referred to here as Resonance Sampling, uses the AC Stark shifts to selectively induce Freeman resonances and is resilient to changes in the spectral phase. Freeman resonances established in this way can result in population inversion of the excited state, and may lead to new lasing mediums and remote sensing applications.
We have observed St\"uckelberg oscillations in the dipole-dipole interaction between Rydberg atoms with an externally applied radio-frequency field. The oscillating rf field brings the interaction between cold Rydberg atoms in two separated volumes into resonance. We observe multiphoton transitions when varying the amplitude of the rf field and the static electric field offset. The angular momentum states we use show a quadratic Stark shift, which leads to a fundamentally different behavior than linearly shifting states. Both cases are studied theoretically using the Floquet approach and are compared. The amplitude of the sidebands, related to the interaction strength, is given by the Bessel function in the linearly shifting case and by the generalized Bessel function in the quadratically shifting case. The oscillatory behavior of both functions corresponds to St\"uckelberg oscillations, an interference effect described by the semiclassical Landau-Zener-St\"uckelberg model. The measurements prove coherent dipole-dipole interaction during at least $0.6\text{ }\ensuremath{\mu}\text{s}$.
We study the dynamics of an atomic Bose-Einstein condensate in an optical lattice in which the electronic ground state of each atom is weakly coupled to a highly excited Rydberg state by a far off-resonant laser. This dressing induces a switchable effective soft-core interaction between ground-state atoms which, in the lattice, gives rise to on-site as well as long-range interaction terms. Upon switching on the dressing laser the coherence properties of the atomic superfluid undergo a nontrivial collapse and revival dynamics which can be observed in the interference pattern that is created after a release of the atoms from the optical lattice. This interference signal strongly depends on the strength and the duration of the dressing laser pulse and can be used to probe and characterize the effective interaction between Rydberg-dressed atoms.
The goal of this work is to study and understand dynamics of atomic systems interacting with strong fields. To this end, a method referred to as strong-field spectroscopy is used, which measures the absorption spectrum of atoms interacting with such fields. In the scope of this work, a technique which allows the simultaneous measurement of absorption spectra of attosecond pulses and their reference signal is developed, which significantly increases the sensitivity to absorption changes. Additionally, a reconstruction method is introduced which retrieves the time-dependent evolution of the dipole response of an atomic system directly from a single absorption spectrum. Strong-field spectroscopy combines these techniques to examine the nonlinear strong-field dynamics in atomic and molecular systems and is applied to study the strongly correlated doubly excited states in helium. Furthermore, a measurement approach is introduced which uses the interaction with a high-intensity laser pulse to impose a time gate on the evolution of the coherent response of a system, which has previously been excited by an ultrashort laser pulse. With this approach the buildup of resonance phenomena in a wide range of physical systems can be studied. As a first application, the time-dependent buildup of a Fano resonance as well as the buildup of a whole Rydberg series are investigated.