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Journal of Physics Conference Series

Watching the emergence of a Fano resonance in doubly excited helium

Alexander Blättermann, Andreas Kaldun, Veit Stooß, Stefan Donsa, Hui Li Wei, Renate Pazourek, Stefan Nagele, Christian Ott, C. D. Lin, Joachim Burgdörfer, Thomas Pfeifer

Published Nov 1, 2017• 2 citations
Publisher

Abstract

We report on the experimental observation of the buildup of the 2s2p Fano resonance in helium in the time domain, which has been under theoretical investigation for more than a decade. The emergence of the absorption line is temporally resolved by interrupting the natural decay of the excited state via saturated strong-field ionization at a variable time delay. We compare the experimental data with full ab-initio simulations to validate the time-gating by strong-field ionization and thereby confirm the recently developed theory for the formation of Fano line-profiles.

DOI
10.1088/1742-6596/875/2/012010

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We report on the experimental observation of the buildup of the 2s2p Fano resonance in helium in the time domain, which has been under theoretical investigation for more than a decade. The emergence of the absorption line is temporally resolved by interrupting the natural decay of the excited state via saturated strong-field ionization at a variable time delay. We compare the experimental data with full ab-initio simulations to validate the time-gating by strong-field ionization and thereby confirm the recently developed theory for the formation of Fano line-profiles.
Strong-field manipulation of autoionizing states is a crucial aspect of electronic quantum control. Recent measurements of the attosecond transient absorption spectrum of helium dressed by a few-cycle visible pulse [Ott et al., arXiv:1205.0519[physics.atom-ph] ] provide evidence of novel ultrafast resonant phenomena, namely, two-photon Rabi oscillations between doubly-excited states and the inversion of Fano profiles. Here we present the results of accurate \emph{ab-initio} calculations that agree with these observations and in addition predict that (i) inversion of Fano profiles is actually periodic in the coupling laser intensity and (ii) the supposedly dark 2p22p^22p2 {1^11S} state also appears in the spectrum. Closer inspection of the experimental data confirms the latter prediction.
Time-resolved buildup of a Fano resonance in a macroscopic gaseous medium is theoretically studied by attosecond transient absorption spectroscopy. An intense near-infrared field is employed as an adjustable gate to confine the temporal dynamics, enabling one to resolve the line-shape formation in real time. Beyond the region where the single-atom approximation holds, we observe the emergence of spectral spikes with narrow linewidths for certain time delays and propagation distances, which represents that the medium can be delicately structured to be an efficient resonant absorber. Spectral substructures appear on the shoulder of the absorption lines after additional pulse propagation. The links between these features imprinted in spectral profiles and the formation of temporal characteristics in the excitation field are identified. The collective response of the medium versus time delay and propagation distance, in this laser-gated case, provides clues to the time-domain information on autoionization state and the microscopic dynamics occurring at each layer of the medium.
In the present paper, we investigate the time-resolved transient absorption spectroscopy of doubly excited states of helium atoms by solving the time-dependent two-electron Schr\"odinger equation numerically based on a one-dimensional model. The helium atoms are subjected to an extreme ultraviolet (XUV) attosecond pulse and a time-delayed infrared (IR) few-cycle laser pulse. A superposition of doubly excited states populated by the XUV pulse is identified, which interferes with the direct ionization pathway leading to Fano resonance profiles in the photoabsorption spectrum. In the presence of an IR laser, however, the Fano line profiles are strongly modified: A shifting, splitting, and broadening of the original absorption lines is observed when the XUV attosecond pulse and infrared few-cycle laser pulse overlap in time, which is in good agreement with recent experimental results. At certain time delays, we observe symmetric Lorentz, inverted Fano profiles, and even negative absorption cross sections indicating that the XUV light can be amplified during the interaction with atoms. We further prove that the above pictures are general for different doubly excited states by suitably varying the frequency of the IR field to coherently couple the corresponding states.
We report time-resolved photoelectron spectroscopy of the 3s3p3s3p3s3p doubly excited states of helium dressed by an intense near-infrared (NIR) laser field. Using synchronized XUV free-electron-laser and 800-nm NIR laser pulses, we observe a pronounced delay-dependent shift of resonance-related spectral minima together with the emergence of additional structures around the NIR sideband energy. \textit{Ab initio} theoretical calculations support these observations and identify the features as signatures of NIR-induced coupling of the bright (3s3p1Po3s3p {}^{1}P^{o}3s3p1Po) autoionizing state to nearby dark (1De^{1}D^{e}1De and 1Se^{1}S^{e}1Se) resonances below the N=3N = 3N=3 threshold. A multichannel Fano resonance analysis of the measured spectra yields delay-dependent line-shape parameters and resonance energies, establishing a quantitative route to characterize and control correlated two-electron resonances in strong laser fields.