Time resolved Coulomb explosion imaging of multi-channel non-adiabatic photodissociation dynamics

ORAL

Abstract

We utilize soft X-ray Free Electron Laser (FEL) pulses to track non-adiabatic and photodissociation dynamics in a series of iodide containing hydrocarbons. A time-stamping camera and a hexanode delay line were utilized at the FLASH and SACLA FEL facilities, respectively, to correlate the ion vector momenta following excitation across the deep ultraviolet. In the FLASH results, predissociation of the B-state in methyl iodide is investigated and photofragment angular distributions are extracted from sliced ion velocity map images. At SACLA, the photoexcitation energy dependence of the A-band in methyl iodide and iodobenzene is explored by using tunable pulses from an optical parametric amplifier. Highlighted is the competition between both direct (excited state) and indirect (ground state) photodissociation pathways, with latter mediated by internal conversion.

*This work was supported by the U.S. Department of Energy, Office of Science, Basic Energy Sciences (BES), Chemical Sciences, Geosciences, and Biosciences Division

Authors

  • Ruaridh Forbes

    • Stanford University
    • PULSE Institute, Stanford University
    • Department of Physics at Stanford University, PULSE Institute
  • Daniel Rolles

    • Kansas State University
    • J.R. Macdonald Lab, Kansas State University
    • J. R. Macdonald Laboratory, Department of Physics, Kansas State University
  • Taran Driver

    • Stanford University
  • Michael Burt

    • Oxford University
  • Mark Brouard

    • Oxford University
  • Philip Bucksbaum

    • Stanford University