4.8 Article

Charge and Nuclear Dynamics Induced by Deep Inner-Shell Multiphoton Ionization of CH3I Molecules by Intense X-ray Free-Electron Laser Pulses

Journal

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 6, Issue 15, Pages 2944-2949

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.5b01205

Keywords

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Funding

  1. program review committee [2012B8045]
  2. X-ray Free Electron Laser Utilization Research Project
  3. X-ray Free Electron Laser Priority Strategy Program of the Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT)
  4. Japan Society for the Promotion of Science (JSPS) [21244062, 23241033]
  5. MEXT [22740264]
  6. Proposal Program of SACLA Experimental Instruments of RIKEN
  7. Academy of Finland
  8. Cooperative Research Program of the Network Joint Research Center for Materials and Devices of MEXT
  9. Chemical Sciences, Geosciences, and Biosciences Division of the Office of Basic Energy Sciences, Office of Science, U.S. Department of Energy
  10. CNRS program PEPS SASELELX
  11. European Cooperation in Science and Technology (COST) action - XUV/x-ray light and fast ions for ultrafast chemistry (XLIC) [CM1204]
  12. JSPS
  13. National Basic Research Program of China [2013CB922200]
  14. NSFC [11274232, 11420101003]
  15. Shanghai Pujiang Program [13PJ1407500]
  16. Global Research Laboratory Program [2009-0439]
  17. Max Planck POSTECH/KOREA Research Initiative Program through the National Research Foundation of Korea (NRF) - Ministry of Science, ICT & Future Planning [2011-0031558]
  18. Grants-in-Aid for Scientific Research [15H02119, 26390019, 22740264, 23241033, 15K17722] Funding Source: KAKEN

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In recent years, free-electron lasers operating in the true X-ray regime have opened up access to the femtosecond-scale dynamics induced by deep inner-shell ionization. We have investigated charge creation and transfer dynamics in the context of molecular Coulomb explosion of a single molecule, exposed to sequential deep inner-shell ionization within an ultrashort (10 fs) X-ray pulse. The target molecule was CH3I, methane sensitized to X-rays by halogenization with a heavy element, iodine. Time-of-flight ion spectroscopy and coincident ion analysis was employed to investigate, via the properties of the atomic fragments, single-molecule charge states of up to +22. Experimental findings have been compared with a parametric model of simultaneous Coulomb explosion and charge transfer in the molecule. The study demonstrates that including realistic charge dynamics is imperative when molecular Coulomb explosion experiments using short-pulse facilities are performed.

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