Transmission of attosecond-pulsed light through Helium gas driven by few-cycle laser fields of tunable intensity allows to temporally resolve and control the process of absorption. The results enabled the understanding of Fano resonances in the time domain and corresponding scientific applications.
Fano Resonances in the Time Domain - understanding and controlling the absorption and emission of light—Within this work, starting from the well known theory for photoabsorption cross sections by Ugo Fano, a new formalism is developed, which enables measurement and control of phase and amplitude changes in an emitting dipole. This is shown by experimental measurements in singly and doubly excited helium that confirm the formalism. An application in time-domain quantum holography of excited states, allowing to separate laser-induced coupling pathways, is also presented.
The attosecond pump-femtosecond probe technique is widely used in electron dynamics research, with temporal resolution reaching tens of attoseconds. Here, we propose a scheme for controlling the Fano line shapes of helium doubly excited states by replacing the pump source with a pair of time-delayed attosecond pulses. We show that the interference induced by this delay provides an additional, highly effective means of controlling electron dynamics, enabling temporal resolution on the zeptosecond scale. We demonstrate that the corresponding line shapes in transient absorption spectra can shift dramatically within a time-delay variation of just a few hundred zeptoseconds. This extreme spectral modulation occurs under two key conditions: (i) when the time delay aligns with the spectral minimum of the coherently combined attosecond pulses in the frequency domain, and (ii) when the delay between the infrared probe pulse and the first attosecond pulse is held constant. This approach opens a new pathway to zeptosecond-scale control in quantum systems and demonstrates the powerful synergy between phase manipulation in both light and electron waves for achieving ultrafast spectral transformations.
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 2p2 {1S} state also appears in the spectrum. Closer inspection of the experimental data confirms the latter prediction.
The past thirty years witnessed rapid developing of strong field physics that leads to the first generation of attosecond (10−18 s) pulses. The duration of available pulses has recently been reduced to less than 100 as, approaching the Kepler period of a classical electron revolving around the nucleus. For the first time, electron motions inside atoms, molecules and solids can be traced, probed and even steered in real time. It pushed the study on ultrafast dynamic processes into a new frontier, giving birth to attosecond physics. The development of attosecond pulses provides unprecedented coherent ultrashort XUV (extreme ultra-violet) of soft X-ray sources that enable imaging the atomic structure and resolving the related quantum dynamics for matter science. In particular, it allows the probing and monitoring of electron dynamics in the natural time scale of attoseconds with atomic spatial resolution. The generation and applications of attosecond pulses are directly related to the control and manipulation of the sub-cycle electron dynamics. Recent studies on the correlated multielectron dynamics have provided insight into the optical and dynamical properties of matter in the perspectives of time, phase and entanglement. It deepens our understanding on some of the fundamental questions, e.g., how the single or multiple photons are absorbed and how short are the quantum processes such as photoionization, tunneling ionization and charge migration. Although currently attosecond pulses are limited by the flux and pulse duration, the combination of attosecond pulses with intense infrared laser pulses paves new ways of controlling and probing electron dynamics in the domains of energy, time and space that lays the foundation for petahertz optoelectronics and attosecond pulse based transient spectroscopy. In this review, we will first briefly summarize the advancement of strong field and ultrafast physics including the relevant experimental findings, the theoretical explorations, the related technologies and the possible applications. Then we focus on the sub-cycle electron or multielectron dynamics and their manifestation on the ionization and coherent radiation properties. We start with the time behavior of Fano resonance and how it can be probed in time domain. In section 2, the correlated electron dynamics is discussed in term of anti-screening effect and Pauli effect that influence strong field ionization and high harmonic generation processes. In section 3, the coherent emission with frequency from terahertz to soft XUV and their joint measurement are discussed by emphasizing the generation mechanism of terahertz wave in two-color laser pulses. The developed high-harmonic and terahertz wave spectroscopy (HATS) is shown capable of imaging the molecular structure and dynamics. In section 4, the time-resolving of electron and hole dynamics and their coherence is proposed based on attosecond transient absorption technique. The coherence of ionization and the correlated electron dynamics is hinted crucial for electron-hole interaction. The topics are very limited and mainly selected from the perspectives of our group.