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1.
Phys Rev Lett ; 131(20): 203201, 2023 Nov 17.
Article in English | MEDLINE | ID: mdl-38039486

ABSTRACT

Multiphoton light-matter interactions invoke a so-called "black box" in which the experimental observations contain the quantum interference between multiple pathways. Here, we employ polarization-controlled attosecond photoelectron metrology with a partial wave manipulator to deduce the pathway interference within this quantum 'black box" for the two-photon ionization of neon atoms. The angle-dependent and attosecond time-resolved photoelectron spectra are measured across a broad energy range. Two-photon phase shifts for each partial wave are reconstructed through the comprehensive analysis of these photoelectron spectra. We resolve the quantum interference between the degenerate p→d→p and p→s→p two-photon ionization pathways, in agreement with our theoretical simulations. Our approach thus provides an attosecond time-resolved microscope to look inside the "black box" of pathway interference in ultrafast dynamics of atoms, molecules, and condensed matter.

2.
Nat Commun ; 13(1): 5072, 2022 Aug 29.
Article in English | MEDLINE | ID: mdl-36038537

ABSTRACT

Attosecond chronoscopy is central to the understanding of ultrafast electron dynamics in matter from gas to the condensed phase with attosecond temporal resolution. It has, however, not yet been possible to determine the timing of individual partial waves, and steering their contribution has been a substantial challenge. Here, we develop a polarization-skewed attosecond chronoscopy serving as a partial wave meter to reveal the role of each partial wave from the angle-resolved photoionization phase shifts in rare gas atoms. We steer the relative ratio between different partial waves and realize a magnetic-sublevel-resolved atomic phase shift measurement. Our experimental observations are well supported by time-dependent R-matrix numerical simulations and analytical soft-photon approximation analysis. The symmetry-resolved, partial-wave analysis identifies the transition rate and phase shift property in the attosecond photoelectron emission dynamics. Our findings provide critical insights into the ubiquitous attosecond optical timer and the underlying attosecond photoionization dynamics.

3.
Eur Phys J D At Mol Opt Phys ; 75(7): 209, 2021.
Article in English | MEDLINE | ID: mdl-34720730

ABSTRACT

The perceived dichotomy between analytical and ab initio approaches to theory in attosecond science is often seen as a source of tension and misconceptions. This Topical Review compiles the discussions held during a round-table panel at the 'Quantum Battles in Attoscience' cecam virtual workshop, to explore the sources of tension and attempt to dispel them. We survey the main theoretical tools of attoscience-covering both analytical and numerical methods-and we examine common misconceptions, including the relationship between ab initio approaches and the broader numerical methods, as well as the role of numerical methods in 'analytical' techniques. We also evaluate the relative advantages and disadvantages of analytical as well as numerical and ab initio methods, together with their role in scientific discovery, told through the case studies of two representative attosecond processes: non-sequential double ionisation and resonant high-harmonic generation. We present the discussion in the form of a dialogue between two hypothetical theoreticians, a numericist and an analytician, who introduce and challenge the broader opinions expressed in the attoscience community.

4.
Phys Rev Lett ; 123(16): 163001, 2019 Oct 18.
Article in English | MEDLINE | ID: mdl-31702341

ABSTRACT

We use R-matrix with time-dependence theory, with spin-orbit effects included, to study krypton irradiated by two time-delayed extreme ultraviolet ultrashort pulses. The first pulse excites the atom to 4s^{2}4p^{5}5s. The second pulse then excites 4s4p^{6}5s autoionizing levels, whose population can be observed through their subsequent decay. By varying the time delay between the two pulses, we are able to control the excitation pathway to the autoionizing states. The use of cross-polarized light pulses allows us to isolate the two-photon pathway, with one photon taken from each pulse.

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