Attosecond Delays in X-ray Molecular Ionization

The photoelectric effect is not truly instantaneous, but exhibits attosecond delays that can reveal complex molecular dynamics. Sub-femtosecond duration light pulses provide the requisite tools to resolve the dynamics of photoionization. Accordingly, the past decade has produced a large volume of wo...

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Veröffentlicht in:arXiv.org 2024-02
Hauptverfasser: Driver, Taran, Mountney, Miles, Wang, Jun, Ortmann, Lisa, Al-Haddad, Andre, Berrah, Nora, Bostedt, Christoph, Champenois, Elio G, DiMauro, Louis F, Duris, Joseph, Garratt, Douglas, Glownia, James M, Guo, Zhaoheng, Haxton, Daniel, Isele, Erik, Ivanov, Igor, Ji, Jiabao, Kamalov, Andrei, Li, Siqi, Ming-Fu, Lin, Marangos, Jon P, Obaid, Razib, O'Neal, Jordan T, Rosenberger, Philipp, Shivaram, Niranjan H, Wang, Anna L, Walter, Peter, Wolf, Thomas J A, Hans Jakob Wörner, Zhang, Zhen, Bucksbaum, Philip H, Kling, Matthias F, Landsman, Alexandra S, Lucchese, Robert R, Emmanouilidou, Agapi, Marinelli, Agostino, Cryan, James P
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Zusammenfassung:The photoelectric effect is not truly instantaneous, but exhibits attosecond delays that can reveal complex molecular dynamics. Sub-femtosecond duration light pulses provide the requisite tools to resolve the dynamics of photoionization. Accordingly, the past decade has produced a large volume of work on photoionization delays following single photon absorption of an extreme ultraviolet (XUV) photon. However, the measurement of time-resolved core-level photoionization remained out of reach. The required x-ray photon energies needed for core-level photoionization were not available with attosecond tabletop sources. We have now measured the x-ray photoemission delay of core-level electrons, and here report unexpectedly large delays, ranging up to 700 attoseconds in NO near the oxygen K-shell threshold. These measurements exploit attosecond soft x-ray pulses from a free-electron laser (XFEL) to scan across the entire region near the K-shell threshold. Furthermore, we find the delay spectrum is richly modulated, suggesting several contributions including transient trapping of the photoelectron due to shape resonances, collisions with the Auger-Meitner electron that is emitted in the rapid non-radiative relaxation of the molecule, and multi-electron scattering effects. The results demonstrate how x-ray attosecond experiments, supported by comprehensive theoretical modelling, can unravel the complex correlated dynamics of core-level photoionization.
ISSN:2331-8422