The electronic structure of atomic quantum systems and their dynamical interaction with light is reflected in transition dipole matrix elements coupling the system's energy eigenstates. In this work, we measure phase shifts of the time-dependent ultrafast absorption to determine the relative signs of. the transition-dipole matrix elements. The measurement relies on precise absolute calibration of the relative timing between the used light pulses, which is achieved by combining attosecond transient absorption and attosecond streaking spectroscopy to simultaneously measure the resonant photoabsorption spectra of laser-coupled doubly excited states in helium, together with the attosecond streaked photoelectron spectra. The streaking measurement reveals the absolute timing and the full temporal profile of the interacting electric fields which is then used to quantify the state-specific dynamics of the measured photoabsorption spectra. By comparing the 1-fs time-scale modulation across the absorption lines corresponding to the 2s2p (1P) and sp2,3+ (1P) doubly excited states between simulation and measurement, we quantify the signs of the transition dipole matrix elements for the laser-coupled autoionizing states 2s2p-2p2 and 2p2-sp2,3+ to be opposite of each other.
We report on the first streaking measurement of water-window attosecond pulses generated via high harmonic generation, driven by sub-2-cycle, CEP-stable, 1850 nm laser pulses. Both the central photon energy and the energy bandwidth far exceed what has been demonstrated thus far, warranting the investigation of the attosecond streaking technique for the soft X-ray regime and the limits of the FROGCRAB retrieval algorithm under such conditions. We also discuss the problem of attochirp compensation and issues regarding much lower photo-ionization cross sections compared with the XUV in addition t…
We employ the R-matrix with time-dependence method to study attosecond angular streaking of F$^-$. Using this negative ion, free of long-range Coulomb interactions, we elucidate the role of short-range electron correlation effects in an attoclock scheme. Through solution of the multielectron time-dependent Schrodinger equation, we aim to bridge the gap between experiments using multielectron targets, and one-electron theoretical approaches. We observe significant negative offset angles in the photoelectron momentum distributions, despite the short-range nature of the binding potential. We show…
The present work focuses on the characterisation of the amount of orbital angular momentum (OAM) encoded in the twisted attosecond pulses via energy- and angle-resolved attosecond streaking in pump-probe setup. It is found that the photoelectron spectra generated by the linearly polarised twisted pulse with different OAM values exhibit angular modulations, whereas circularly polarised twisted pulse yields angular isotropic spectra. It is demonstrated that the energy- and angle-resolved streaking spectra are sensitive to the OAM values of the twisted pulse. Moreover, the different combinations …
Streaking of photoelectrons has long been used for the temporal characterization of attosecond extreme ultraviolet pulses. When the time-resolved photoelectrons originate from a coherent superposition of electronic states, they carry an additional phase information, which can be retrieved by the streaking technique. In this contribution we extend the streaking formalism to include coupled electron and nuclear dynamics in molecules as well as initial coherences and demonstrate how it offers a novel tool to monitor non-adiabatic dynamics as it occurs in the vicinity of conical intersections and …
The use of semiclassical models based on the Strong Field Approximation (SFA) is ubiquitous in strong field multi-photon ionization and underlies many key developments in attosecond science, including the description of High Harmonic Generation (HHG). However, such models are notably lacking in streaking experiments, which use an attosecond pulse to initiate single-photon ionization and a lower frequency infrared pulse to provide timing information. Here, we introduce a classical Wigner propagation (CWP) method, which analogously to semiclassical models in strong field ionization, treats the i…
Tunnelling, one of the key features of quantum mechanics, ignited an ongoing debate about the value, meaning and interpretation of 'tunnelling time'. Until recently the debate was purely theoretical, with the process considered to be instantaneous for all practical purposes. This changed with the development of ultrafast lasers and in particular, the 'attoclock' technique that is used to probe the attosecond dynamics of electrons. Although the initial attoclock measurements hinted at instantaneous tunnelling, later experiments contradicted those findings, claiming to have measured finite tunne…
Time-resolved electronic processes on the attosecond scale have recently become experimentally accessible through the development of laser-based pump-probe interrogation techniques such as the attosecond streak camera, the reconstruction of attosecond beating by interference of two-photon transitions, and the attoclock. In this work, we demonstrate that by combining the concepts of the attosecond streak camera and the attoclock, time resolved processes down to the time scale of tens of zeptoseconds come into reach. Key to advancing to this remarkable level of time precision by this method term…
Attosecond angular streaking, also known as the "attoclock", employs a short elliptically polarized laser pulse to tunnel ionize an electron from an atom or a molecule and to put a time stamp on this process by deflecting the photoelectron in the angular spatial direction. This deflection can be used to evaluate the time the tunneling electron spends under the classically inaccessible barrier and to determine whether this time is finite. In this review, we examine the latest experimental and theoretical findings and present a comprehensive set of evidence supporting the zero tunneling time sce…
