APS Logo

Insights into ultrafast excited state dynamics by combining theory and experiment

ORAL · Invited

Abstract

A main focus of our work is to develop our understanding of ultrafast excited state processes in molecules using a closely collaborative approach between theory and experiment. To achieve this goal we use theoretical calculations to reproduce experimental observables from different experimental probes. Nonadiabatic excited state dynamics are carried out employing the trajectory surface hopping approach combined with multireference electronic structure methods. The dynamics are used to model various experimental observables, such as time resolved photoelectron spectra, ultrafast electron diffraction signals and Coulomb explosion imaging.

In recent efforts we have focused on understanding better Coulomb explosion imaging by modeling dissociation of multiply charged molecules. Important insights from these studies will be discussed.

Publication: Statistical vs Directed Dissociation of Molecular Dications<br>V Singh, G Mogol, Y Bodek, C Cheng, C Trallero, T Weinacht, S Matsika<br>In preparation (2025)<br><br>Quantum contributions to Coulomb-explosion imaging revealed by trajectory-surface-hopping molecular dynamics<br>V Singh, C Cheng, T Weinacht, S Matsika<br>Physical Review A 109 (5), 052813 (2024)<br><br>Strong field double ionization of formaldehyde investigated using momentum resolved covariance imaging and trajectory surface hopping<br>C Cheng, V Singh, S Matsika, T Weinacht<br>The Journal of Physical Chemistry A 126 (40), 7399-7406 (2022)

Presenters

  • Spiridoula C Matsika

    Temple University

Authors

  • Spiridoula C Matsika

    Temple University

  • Vaibhav Singh

    Temple University

  • Chuan Cheng

    Stanford University

  • Thomas Weinacht

    Stony Brook University (SUNY), Stony Brook University