Temporal Observation of Interchannel Coupling in Molecular Photoionization

ORAL

Abstract

Molecular photoionization delays are measured for the X $^{2}\Pi_{g}$, A $^{2}\Pi_{u}$, and B $^{2}\Sigma^{+}_{u}$ cationic states of CO$_2$ using the Reconstruction of Attosecond Beating By Interference of Two-photon Transitions (RABBITT) technique. We compare these measured values with quantum mechanical calculation of the photoionization scattering phase. Our results show that interchannel continuum coupling is necessary to explain the observed result. Moreover, this interchannel continuum coupling is particularly important in the vicinity of a molecular shape resonance and near autoionizing molecular Rydberg states. This approach is a first step towards time-resolving electron correlation in molecular photoionization.

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

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Authors

  • Andrei Kamalov

    • Stanford PULSE Institute, SLAC National Accelerator Laboratory

  • Philip H. Bucksbaum

    • Stanford PULSE Institute, SLAC National Accelerator Laboratory

  • Daniel J. Haxton

    • KLA Corporation

  • James P. Cryan

    • PULSE Institute, Linac Coherent Light Source, SLAC National Accelerator Laboratory
    • Stanford PULSE Institute, SLAC National Accelerator Laboratory; Linac Coherent Light Source, SLAC National Accelerator Laboratory
    • Stanford PULSE Institute, SLAC National Accelerator Laboratory