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Acta Physica Sinica

Theoretical study of the periodic quantum phase modulation of the dipole response in atomic He

Jingjie Ding, Quanjun Wang, Zuoye Liu, Hu Bi-Tao

Published Jan 1, 2015• 0 citations
Publisher

Abstract

Based on the laser-induced-phase model, periodic quantum phase modulation of the dipole response in atomic He is studied theoretically. The two-level system of the transition 1s2→1s2p with a delay width of 1.8 × 109 s-1 and an energy difference of 21.2 eV between the excited state and the ground state is used in the calculation. The system is excited by attosecond laser pulse from high harmonic generator, and the spectral response of the system is of single isolated symmetric Lorentzian absorption line. After the excitation, near infrared (NIR) femtosecond laser pulse train with a repetition rate of 5 GHz, central frequency 780 nm, and pulse duration of 100 fs, is utilized to periodically modify the spontaneous decay of the excited 1s2p level. The incremental phase step Δφ depends on the intensity of the NIR laser pulse, while the initial offset phase φ can be controlled independently by partially overlapping the first NIR pulse with the excitation. Simulated results show that the Lorentzian absorption line is transformed into comb-like spectral structure with equal gap depending on the repetition rate of the NIR pulse train. The line shape of each comb tooth is symmetric Lorentzian line by setting φ = Δφ/2 = π/2, while it is Fano line by setting φ = Δφ = π. The location of the comb structure is mainly dependent on the energy difference between the excited state and the ground state, while it can be slightly tuned by controlling the incremental phase step Δφ. We develop an analytic description of the comb-like spectral structure by Fourier analysis, depending on both the atomic and the phase-control properties. The analytical expressions can be readily used to estimate the exact experimental parameters. The universality of this mechanism allows the spectral modulation in arbitrary atomic system at arbitrary frequency, including the hard X-ray regime, by using reference transitions in highly charged ions. The generalization of this approach should thus not only enable relative frequency measurement and relevant applications at extremely high frequencies, but also open the way for pulse shaping at arbitrary frequencies.

DOI
10.7498/aps.64.243201

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Based on the laser-induced-phase model, periodic quantum phase modulation of the dipole response in atomic He is studied theoretically. The two-level system of the transition 1s2→1s2p with a delay width of 1.8 × 109 s-1 and an energy difference of 21.2 eV between the excited state and the ground state is used in the calculation. The system is excited by attosecond laser pulse from high harmonic generator, and the spectral response of the system is of single isolated symmetric Lorentzian absorption line. After the excitation, near infrared (NIR) femtosecond laser pulse train with a repetition rate of 5 GHz, central frequency 780 nm, and pulse duration of 100 fs, is utilized to periodically modify the spontaneous decay of the excited 1s2p level. The incremental phase step Δφ depends on the intensity of the NIR laser pulse, while the initial offset phase φ can be controlled independently by partially overlapping the first NIR pulse with the excitation. Simulated results show that the Lorentzian absorption line is transformed into comb-like spectral structure with equal gap depending on the repetition rate of the NIR pulse train. The line shape of each comb tooth is symmetric Lorentzian line by setting φ = Δφ/2 = π/2, while it is Fano line by setting φ = Δφ = π. The location of the comb structure is mainly dependent on the energy difference between the excited state and the ground state, while it can be slightly tuned by controlling the incremental phase step Δφ. We develop an analytic description of the comb-like spectral structure by Fourier analysis, depending on both the atomic and the phase-control properties. The analytical expressions can be readily used to estimate the exact experimental parameters. The universality of this mechanism allows the spectral modulation in arbitrary atomic system at arbitrary frequency, including the hard X-ray regime, by using reference transitions in highly charged ions. The generalization of this approach should thus not only enable relative frequency measurement and relevant applications at extremely high frequencies, but also open the way for pulse shaping at arbitrary frequencies.
Line shapes observed in attosecond transient absorption spectra (ATAS) encode information on the phase of the optical dipole response. Understanding and controlling the phase evolution of interference fringes is among the fundamental goals of exploring coherent interaction. Here, we simulate the attosecond transient absorption in the near-infrared (NIR) dressing field by considering a three-level model in the adiabatic approximation. We find that the absorption line shape can be changed from Lorentzian to Fano to inverted Lorentzian and back again at two-photon dressed energy levels “ω ± 2ωι”, and line shapes evolve in half-cycle periodicity (T/2). Moreover, the direction of phase evolution of “ω ± 2ωι” is opposite, while the phases of “ω ± 2ωι” are roughly the same at certain delays with an interval of approximately a quarter-cycle periodicity (T/4). These results demonstrate that absorbance of two-photon dressed energy levels “ω ± 2ωι” can qualitatively map the AC Stark shift. These observations provide new insights into the control of spectral line shapes and open the way for the modulation of quantum optical interference in the laser-driven atom.
In this work, the strong-field-modified dipole response at the ionization threshold of helium is studied. The dipole response is induced by an attosecond pulse in the extreme ultraviolet spectral range and is manipulated by an ultrashort and strong femtosecond pulse in the near-infrared. To probe the response, the transient absorption spectrum of helium is recorded for different time delays between both pulses and different intensities of the femtosecond pulse. From the spectra, the dipole response of the ionization threshold is reconstructed, which is linked to the dynamics of excited electrons with energies in the transition region from bound to free. To identify the underlying processes of light-matter interaction leading to the observed structures in the time and spectral domain, different quantum-mechanical model simulations are conducted. As a result, the measured dipole response reveals light-induced energy shifts of the photoelectron’s kinetic energy close to the parent ion, signatures for field-driven recollisions of a photoelectron into the parent ion, and a temporal amplitude and phase gating mechanism. With the latter, the build-up dynamics of complex spectral structures are temporally resolved, which are the time-dependent separation and line-shape modification of the doubly excited Rydberg series as well as the temporal build-up of the ionization threshold.
Symmetric Lorentzian and asymmetric Fano line shapes are fundamental spectroscopic signatures that quantify the structural and dynamical properties of nuclei, atoms, molecules, and solids. This study introduces a universal temporal-phase formalism, mapping the Fano asymmetry parameter q to a phase φ of the time-dependent dipole response function. The formalism is confirmed experimentally by laser-transforming Fano absorption lines of autoionizing helium into Lorentzian lines after attosecond-pulsed excitation. We also demonstrate the inverse, the transformation of a naturally Lorentzian line into a Fano profile. A further application of this formalism uses quantum-phase control to amplify extreme-ultraviolet light resonantly interacting with He atoms. The quantum phase of excited states and its response to interactions can thus be extracted from line-shape analysis, with applications in many branches of spectroscopy.
The coherent excitation and manipulation of a two-level system with ultrashort intense extreme-ultraviolet laser fields is investigated theoretically, based on numerically solving the time-dependent Schr\"odinger equation. We are particularly interested in the dynamical phase excursion of the energy states over the course of the interaction and the resulting spectral modifications. Fitting the absorption line shapes with the Fano profile quantifies the asymmetry parameter and the corresponding dipole phase offset, capturing the phase difference of the state coefficients after the interaction. Nonperturbative analytical calculations using rectangular driving pulses are employed, yielding physical insights into the dependence of the dipole phase shift on the external field. The validity of the formulas is validated by comparing their predictions with numerical results, which proves to be robust against the variation of laser parameters. The present investigation of strong-field dressing effects complements recent attosecond transient absorption studies assuming weak excitation, and marks a ubiquitous phenomenon that should be generally considered for the interaction of matter with intense laser fields.
Advancements in x-ray sources extend the scope of light-matter interactions into the x-ray-nuclear regime. Precise temporal control of quantum phases provides fundamental insights into quantum systems and serves as a cornerstone for numerous quantum technologies. Nevertheless, achieving phase control of quantum systems with high temporal and spatial resolution remains a substantial challenge in the realm of hard x-ray quantum optics due to the ultrashort oscillation periods of photons. In this study, we propose to manipulate the magnetic properties of a thin 57Fe^{57}\text{Fe}57Fe film using near-infrared (NIR) pulses characterized by a high repetition rate. By calculating the evolution of quantum beats, we can theoretically extract the phase information of the nuclear response. Coherence within the nuclear ensemble is preserved throughout the entire process. This control scheme achieves quantum shifts with zeptosecond precision and modulates the spectral line shape within the frequency domain. Our proposal introduces a high-resolution method for rapidly manipulating nuclear states using optical laser pulses.
Laser-dressed absorption in atomic helium is studied, both theoretically and experimentally, by transient absorption spectroscopy using isolated 400-as pulses centered at 22 eV and 12-fs near-infrared (NIR) pulses with 780-nm central wavelength. Multiple features in the helium singly excited bound-state spectrum are observed only when the NIR and attosecond pulses are overlapped in time. Theoretical analysis indicates that these light-induced structures (LISs) are the intermediate states in resonant, second-order processes that transfer population to multiple dipole forbidden states. The use of broadband, coherent extreme ultraviolet (XUV) radiation allows observation of these LISs without specifically tuning to a two-photon resonance, as would be required with narrowband XUV light. The strength and position of the LISs depend strongly on the NIR intensity and the pump-probe delay.