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Updated: May 12, 2026

Measurement of Ultrafast Vibrational Coherences in Polyatomic Radical Cations with Strong-Field Adiabatic Ionization
Published on: August 6, 2018
Time-domain Measurement of Auger Electron Dynamics in Xenon and Krypton Atoms after Giant Resonance Photoionization
Mahmudul Hasan1, Jingsong Gao1, Hao Liang2
1Kansas State University, James R. Macdonald Laboratory, Department of Physics, Manhattan, Kansas 66506, USA.
Abstract:
Time-resolved measurement of Auger-Meitner decay [Drescher et al., Nature (London) 419, 803 (2002)NATUAS0028-083610.1038/nature01143] marked a milestone in the development of attosecond science. To date, the time constants for the Auger-Meitner decay processes obtained from the time-domain experiments were found to be consistent with the values deduced from conventional energy-domain measurements. One of the main factors limiting the temporal resolution of these studies is the unlocked carrier-envelope-phase (CEP) of the laser pulses used to probe the electronic dynamics triggered by inner-shell photoabsorption. In this Letter, we report time-resolved inner-shell electron spectroscopy of xenon and krypton using attosecond soft x-ray (atto-SXR) pulses centered at 130 eV in combination with CEP-stabilized few-cycle Yb laser pulses. We observed that the N_{4,5}OO Auger electrons from xenon exhibit a clear streaking pattern, but with an unexpected time shift of ∼1.32 fs relative to the 4d photoelectrons. Furthermore, the energy-integrated yield of streaked Auger electrons from xenon exhibits a pronounced minimum at a pump-probe time delay of 4 fs. Neither of these observations can be explained by current streaking theories and both are inconsistent with lifetimes inferred from energy-domain measurements. The M_{4,5}NN Auger electrons from krypton partly overlap in energy with the 3d inner-shell photoelectrons and do not show these anomalous features. This Letter offers new insights into the inner-shell electron dynamics of heavy atoms in the giant dipole resonance region, laying the groundwork for attosecond soft x-ray spectroscopy of molecular systems containing iodine or bromine atoms.
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