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Attosecond Electron Correlation Dynamics in Double Ionization of Benzene Probed with Two-Electron Angular Streaking
Alexander H Winney1, Suk Kyoung Lee1, Yun Fei Lin1
1Department of Chemistry, Wayne State University, Detroit, Michigan 48202, USA.
We measured electron emission time delays using advanced imaging. In benzene, double ionization decreased with increasing delay, revealing laser-induced electron correlation
Area of Science:
- Atomic and Molecular Physics
- Quantum Dynamics
- Strong Field Physics
Background:
- Understanding electron correlation is crucial for describing molecular ionization dynamics.
- Strong field physics investigates matter's response to intense laser fields.
- Previous studies lacked precise measurements of electron emission timing in complex molecules.
Purpose of the Study:
- To precisely measure the time delay between sequential electron emissions in benzene.
- To investigate the role of electron correlation in strong field double ionization.
- To explore the influence of laser polarization on ionization dynamics.
Main Methods:
- Developed a novel three-dimensional electron-electron coincidence imaging technique.
- Employed a two-electron angular streaking method for time delay measurements.
- Utilized a nearly circularly polarized laser field to drive benzene ionization.
Main Results:
- Successfully measured electron emission time delays ranging from tens of attoseconds to over 1 femtosecond.
- Observed a surprising decay in the benzene double ionization rate within the first 500 attoseconds of electron emission.
- Correlated the ionization decay with the reduction of Coulomb repulsion perpendicular to laser polarization.
Conclusions:
- Laser-induced electron correlation significantly impacts strong field double ionization in benzene.
- The observed decay highlights the complex interplay between electron dynamics and laser fields.
- This work provides new insights into attosecond electron correlation phenomena in molecules.
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