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Updated: Jun 26, 2026

Measurement of Ultrafast Vibrational Coherences in Polyatomic Radical Cations with Strong-Field Adiabatic Ionization
Published on: August 6, 2018
Ultrafast laser-driven excitation dynamics in ne: an ab initio time-dependent R-matrix approach
M A Lysaght1, P G Burke, H W van der Hart
1Centre for Theoretical Atomic, Molecular and Optical Physics, Queen's University Belfast, Belfast BT7 1NN, United Kingdom.
Abstract:
An attosecond pump-probe scheme that combines the use of a free-electron laser pulse with an ultrashort pulse is applied in order to explore the ultrafast excitation dynamics in Ne. We describe the multielectron dynamics using a new nonperturbative time-dependent R-matrix theory. This theory enables the interaction of ultrashort light fields with multielectron atoms and atomic ions to be determined from first principles. By probing the emission of an inner 2s electron from Ne we are also able to study the bound state population dynamics during the free-electron laser pulse.
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