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arXiv:2312.12076

Circularly polarized RABBIT applied to a Rabi-cycling atom

Yijie Liao, Edvin Olofsson, Jan Marcus Dahlström, Liang-Wen Pi, Yueming Zhou, Peixiang Lu

Published Dec 19, 2023• 0 citations
arXivHTMLPDF

Abstract

We utilize the reconstruction of attosecond beating by interference of two-photon transitions (RABBIT) technique to study the phase of a Rabi-cycling atom using circularly polarized extreme ultraviolet and infrared (IR) fields, where the IR field induces Rabi oscillations between the 2s and 2p states of lithium. Autler-Townes splittings are observed in sidebands of the photoelectron spectra and the relative phases of outgoing electron wave packets are retrieved from the azimuthal angle. In this RABBIT scheme, more ionization pathways beyond the usual two-photon pathways are required. Our results show that the polar-angle-integrated and polar-angle-resolved RABBIT phases have different behaviors when the XUV and IR fields have co- and counter-rotating circular polarizations, which are traced back to the different ionization channels according to the selection rules in these two cases and their competition relying on the propensity rule in laser-assisted photoionization.

DOI
10.48550/arxiv.2312.12076

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We utilize the reconstruction of attosecond beating by interference of two-photon transitions (RABBIT) technique to study the phase of a Rabi-cycling atom using circularly polarized extreme ultraviolet and infrared (IR) fields, where the IR field induces Rabi oscillations between the 2s and 2p states of lithium. Autler-Townes splittings are observed in sidebands of the photoelectron spectra and the relative phases of outgoing electron wave packets are retrieved from the azimuthal angle. In this RABBIT scheme, more ionization pathways beyond the usual two-photon pathways are required. Our results show that the polar-angle-integrated and polar-angle-resolved RABBIT phases have different behaviors when the XUV and IR fields have co- and counter-rotating circular polarizations, which are traced back to the different ionization channels according to the selection rules in these two cases and their competition relying on the propensity rule in laser-assisted photoionization.
We utilize the reconstruction of attosecond beating by interference of two-photon transitions (RABBITT) technique to study the phase of a Rabi-cycling atom using circularly polarized extreme ultraviolet and infrared fields, where the infrared field induces Rabi oscillations between the 2s2s2s and 2p2p2p states of lithium. Autler-Townes splittings are observed in sidebands of the photoelectron spectra and the relative phases of outgoing electron wave packets are retrieved from the azimuthal angle. In this RABBITT scheme, more ionization pathways beyond the usual two-photon pathways are required. Our results show that the polar-angle-integrated and polar-angle-resolved RABBITT phases have different behaviors when the extreme ultraviolet and infrared fields have co- and counter-rotating circular polarizations, which are traced back to the different ionization channels according to the selection rules in these two cases and their competition relying on the propensity rule in laser-assisted photoionization.
We present numerical simulations of the reconstruction of attosecond beating by interference of two-photon transitions (RABBITT) on lithium by solving the three-dimensional time-dependent Schr\"odinger equation. In our scheme, the infrared (IR) field couples the 2s2s2s and 2p2p2p states of lithium and leads to the Rabi oscillations of populations between these two states. We analyzed the RABBITT phases of the two peaks in the Rabi-oscillation-induced Autler-Townes splittings. Our results show that the relative phase between these two peaks changes with the photoelectron energy and depends on the intensity of the IR field. Moreover, in the angle-resolved RABBITT measurement, the phases of the two peaks depend differently on the emission angle of photoelectrons. These behaviors are traced back to the different initial phases of the electron wave packets emitted from the dressed 2p2p2p states and the competition among different ionization channels.
We theoretically investigate the resonant two-photon ionization of a hydrogen atom in the counter-rotating circularly polarized double-pulse sequences, by solving the time-dependent Schr\"odinger equation. Due to the induced Rabi oscillations between the ground and excited states, the well-known Autler-Townes doublet is observed in the photoelectron spectra. More interestingly, our numerical results reveal an additional peak located between the Autler-Townes doublets, which originates from single-photon ionization from the excited state by the second pulse. By adjusting the laser intensity of the two pulses, the photoelectron yields of the three peaks can be sensitively modulated, under the control of completed Rabi cycles within the first pulse. In addition, our results show a potential of manipulating the photoemission anisotropy by both the laser intensity and the two-pulse time delay, through adjusting the competition of different partial waves generated by the two pulses.
We theoretically study the infrared (IR)-dressed photoionization of atoms excited by extreme ultraviolet attosecond pulse trains above ionization threshold. The initial state of atoms is treated perturbatively by the IR field, and the continuum states are considered as Coulomb–Volkov (CV) waves. CV waves can much reduce the gauge difference calculated with Volkov waves, and, in general, the contribution of ground-state perturbation to the photoelectron spectrum is negligible. Our calculations show qualitative agreement with the experimental results [Phys. Rev. Lett. 95, 013001 (2005)]. An evident dependence of the photoelectron spectrum on the delay phase between the IR field and the attosecond pulse train is exhibited in both helium and argon. The angular distribution of photoelectrons with various IR polarizations and the corresponding photoelectron spectra are presented. The linearly polarized IR fields are shown to have a higher controlling capability of the spectrum via IR delay phases than the circularly polarized fields. On the other hand, the circularly polarized IR fields have a fruitful angular dependence of photoelectrons with various IR delay phases.
The reconstruction of attosecond beating by interference of two-photon transitions (RABBITT) method is a leading technique for time-resolved investigation of photoionization processes. Interpretation of RABBITT spectra is limited to a lowest-order description, while new variants of the technique necessitate higher intensity infrared fields where this description breaks down. Here, we present an extension of RABBITT theory which can account for higher-order processes (RABBITT-HOP), and demonstrate RABBITT-HOP's ability to predict and describe higher-order processes through simulation of a RABBITT experiment targeting the high-lying 1 s n p Rydberg series of helium. We demonstrate that the signature line shape imparted by the resonances in the 2 ω phase of the lowest sideband can also be observed in the 2 ω phase of the next mainband, as well as in the 4 ω phases of the next sideband and mainband—each with additional phase shifts predicted under RABBITT-HOP. Repeating this analysis for a range of infrared intensities, we determine the lower limits of intensities required for these higher-order processes to become observable and upper limits beyond which nonperturbative effects begin to dominate. This new theoretical framework forms a much-needed basis for accurate interpretation of RABBITT spectra in experiments involving more intense fields, and paves the way for the development of new RABBITT-like techniques which take advantage of this new understanding of how atomic resonance effects may be propagated beyond their nearest sideband.
We study the photoelectron spectra of hydrogen and helium ionized by intense ultrafast two-color XUV laser pulses by numerically solving the time-dependent Schrödinger equation.The photon energy of the pump pulse is tuned to the 1s-2p excitation energy, inducing Rabi oscillations between these bound states and forming an Autler-Townes (AT) doublet of dressed states.When ionized by a time-delayed ultrafast XUV pulse with duration shorter than the Rabi oscillation period, we find novel and drastically enhanced AT splittings in the photoionization spectrum.We identify their origin in terms of the temporal interference of two attosecond wave packets whose spectral distribution is controlled by the interplay between Rabi frequency and bandwidth of the probe pulse.These time-dependent features in the spectra can be much larger than the standard AT spacing induced by the pump pulse alone and can be controlled by the time delay and the duration of the probe pulse.