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Updated: Jun 15, 2025

Measurement of Ultrafast Vibrational Coherences in Polyatomic Radical Cations with Strong-Field Adiabatic Ionization
Published on: August 6, 2018
Attosecond delays in X-ray molecular ionization.
Taran Driver1,2, Miles Mountney3, Jun Wang4,5,6
1Stanford PULSE Institute, SLAC National Accelerator Laboratory, Menlo Park, CA, USA. tdriver@stanford.edu.
Photoelectron emission is not instantaneous, with attosecond delays revealing molecular dynamics. New X-ray attosecond experiments measure these core-level delays, uncovering complex electron interactions.
Area of Science:
- Atomic and Molecular Physics
- Quantum Dynamics
- Ultrafast Science
Background:
- The photoelectric effect exhibits attosecond delays, offering insights into molecular dynamics.
- Sub-femtosecond light pulses enable the study of photoionization dynamics.
- Time-resolved core-level photoionization measurements were previously limited by X-ray source availability.
Purpose of the Study:
- To measure time-resolved X-ray photoemission delays of core-level electrons.
- To investigate the complex dynamics of core-level photoionization using attosecond X-ray pulses.
- To explore contributions to photoemission delays, including electron trapping and scattering.
Main Methods:
- Utilized attosecond soft X-ray pulses from a free-electron laser.
- Performed measurements of X-ray photoemission delay near the oxygen K-shell threshold in NO.
- Scanned the K-shell threshold region to analyze delay spectra.
Main Results:
- Observed unexpectedly large X-ray photoemission delays for core-level electrons, up to 700 attoseconds.
- Found that the delay spectrum is richly modulated, indicating complex electronic processes.
- Identified contributions from transient electron trapping, Auger-Meitner electron collisions, and multi-electron scattering.
Conclusions:
- X-ray attosecond experiments can resolve time-resolved core-level photoionization dynamics.
- The observed delays and spectral modulations provide a detailed view of electron correlations.
- This work opens new avenues for studying molecular dynamics with high temporal resolution.
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