Attosecond Time Delay Trends across the Isoelectronic Noble Gas Sequence

Abstract

The analysis and measurement of Wigner time delays can provide detailed information about the electronic environment within and around atomic and molecular systems, with one the key differences being the lack of a long-range potential after a halogen ion undergoes photoionization. In this work, we use relativistic random-phase approximation to calculate the average Wigner delay from the highest occupied subshells of the atomic pairings (2p, 2s in Fluorine, Neon), (3p, 3s in Chlorine, Argon), (4p, 4s, 3d, in Bromine, Krypton), and (5p, 5s, 4d in Iodine, Xenon). The qualitative behaviors of the Wigner delays between the isoelectronic pairings were found to be similar in nature, with the only large differences occurring at photoelectron energies less than 20 eV and around Cooper minima. Interestingly, the relative shift in Wigner time delays between negatively charged halogens and noble gases decreases as atomic mass increases. All atomic pairings show large differences at low energies, with noble gas atoms showing large positive Wigner delays, while negatively charged halogen ions show negative delays. The implications for photoionization studies in halide-containing molecules is also discussed.

Understanding attosecond streaking

“…it is measurement-dependent. One usually tries to correct for this measurement-dependent effect by splitting the measured streaking delay t s into a Coulomb-laser-coupling term, t CLC , that depends on the probing IR field, and a so-called Eisenbud-Wigner-Smith (EWS) term that is independent of the IR field and that is considered as the 'actual' ionization delay [8,10,25,27,[35][36][37][38][39][40][41][42]:…”