期刊
PHYSICAL REVIEW A
卷 105, 期 5, 页码 -出版社
AMER PHYSICAL SOC
DOI: 10.1103/PhysRevA.105.053102
关键词
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资金
- U.S. Department of Energy, Office of Science, Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division [DE-SC0019451, DE-FG02-86ER13491]
- Deutsche Forschungsgemeinschaft (DFG) [Sonderforschungsbereich 1319]
- Volkswagen foundation within a Peter Paul Ewald-fellowship
- Cluster of Excellence Advanced Imaging of Matter of the DFG [EXC 2056, 390715994]
- DFG, German Research Foundation [SFB-925, 170620586]
This study reports on the observation of resonance effects in molecule CH3I induced by intense x-ray pulses, leading to photon-energy-dependent shift of resonance-induced structures in ion charge state distributions. By comparing the ion charge state distribution of CH3I with that from ionization of atomic xenon, molecule-specific features attributed to ultrafast intramolecular charge rearrangement were observed. Additionally, the study experimentally demonstrates that charge-rearrangement-enhanced x-ray ionization of molecules also plays a role in the soft x-ray regime, previously identified with hard x rays.
Extremely high charge states of atoms and molecules can be created when they are irradiated by intense x-ray pulses. At certain x-ray photon energies, electron ejection from atoms can be drastically enhanced by transient resonances created during the sequential ionization process. Here we report on the observation of such resonance effects in a molecule, CH3I, and show the photon-energy-dependent shift of resonance-induced structures in ion charge state distributions. By comparing the ion charge state distribution of CH3I with that from ionization of atomic xenon, molecule-specific features are observed, which can be attributed to ultrafast intramolecular charge rearrangement. In addition, we experimentally demonstrate that the charge-rearrangement-enhanced xray ionization of molecules, previously found with hard x rays, also plays a role in the soft x-ray regime.
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