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Updated: Aug 21, 2025

Measurement of Ultrafast Vibrational Coherences in Polyatomic Radical Cations with Strong-Field Adiabatic Ionization
Published on: August 6, 2018
Characterizing coherences in chemical dynamics with attosecond time-resolved x-ray absorption spectroscopy
Yuki Kobayashi1, Stephen R Leone2
1Stanford PULSE Institute, SLAC National Accelerator Laboratory, Menlo Park, California 94025, USA.
Time-resolved x-ray absorption spectroscopy (tr-XAS) advances the study of quantum coherence in materials. This technique uses attosecond pulses to reveal electronic and nuclear dynamics, enabling new functionalities beyond thermodynamic limits.
Area of Science:
- Chemical Physics
- Materials Science
- Quantum Dynamics
Background:
- Coherent phenomena drive wave-like motion in photoexcited systems, offering efficient material functionalities.
- Direct characterization of coherence is challenging, making it a key focus in chemical physics.
Purpose of the Study:
- To highlight advances in time-resolved x-ray absorption spectroscopy (tr-XAS) for investigating coherent phenomena.
- To showcase the application of isolated attosecond pulses in studying these dynamics.
Main Methods:
- Utilizing time-resolved x-ray absorption spectroscopy (tr-XAS).
- Employing isolated attosecond pulses for high time and state sensitivity.
- Leveraging element specificity for studying valence electronic dynamics.
Main Results:
- Demonstrated tr-XAS capabilities in characterizing coupled electronic-structural coherence in small molecules.
- Showcased the study of coherent light-matter interactions of core-excited excitons in solids.
- tr-XAS enables detailed investigation of electronic dynamics across various materials.
Conclusions:
- tr-XAS is a powerful method for exploring coherent phenomena due to its sensitivity and specificity.
- Future developments in theory and light sources will enhance tr-XAS's role in understanding chemical dynamics.
- Potential applications span energy, biological systems, and quantum materials.
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