Strong Field Molecular Ionization in the Impulsive Limit: Freezing Vibrations with Short Pulses
arXiv:1611.09142 · doi:10.1103/PhysRevLett.116.063002
Abstract
We study strong-field molecular ionization as a function of pulse duration. Experimental measurements of the photoelectron yield for a number of molecules reveal competition between different ionization continua (cationic states) which depends strongly on pulse duration. Surprisingly, in the limit of short pulse duration, we find that a single ionic continuum dominates the yield, whereas multiple continua are produced for longer pulses. Using calculations which take vibrational dynamics into account, we interpret our results in terms of nuclear motion and non-adiabatic dynamics during the ionization process.
References in corpus (2)
Cited by in corpus (8)
- Equation-of-Motion Coupled-Cluster Theory based on the 4-component Dirac-Coulomb(-Gaunt) Hamiltonian. Energies for single electron detachment, attachment and electronically excited states
- High-order harmonic generation in polyatomic molecules induced by a bicircular laser field
- Strong Field Ionization of Water II: Electronic and Nuclear Dynamics En Route to Double Ionization
- Nonadiabatic dynamics and multiphoton resonances in strong field molecular ionization with few cycle laser pulses
- Direct Observation of Molecular Oxygen Production from Carbon Dioxide
- Experimental Separation of Sub-Cycle Ionization Bursts in Strong-Field Double Ionization of H
- Strong-field chiral imaging with twisted photoelectrons
- Ultrafast Photodissociation Dynamics and Nonadiabatic Coupling Between Excited Electronic States of Methanol Probed by Time-Resolved Photoelectron Spectroscopy