Coincident angle-resolved state-selective photoelectron spectroscopy of acetylene molecules: a candidate system for time-resolved dynamics
Year: 2021
Type: article
Abstract: The acetylene-vinylidene system serves as a benchmark for investigations of ultrafast dynamical processes where the coupling of the electronic and nuclear degrees of freedom provides a fertile playground to explore the femto- and sub-femto-second physics with coherent extreme-ultraviolet (EUV) photon sources both on the table-top as well as free-electron lasers. We focus on detailed investigations of this molecular system in the photon energy range 19-40 eV where EUV pulses can probe the dynamics effectively. We employ photoelectron-photoion coincidence (PEPICO) spectroscopy to uncover hitherto unrevealed aspects of this system. In this work, the role of excited states of the C2H2+ cation, the primary photoion, is specifically addressed. From photoelectron energy spectra and angular distributions, the nature of the dissociation and isomerization channels is discerned. Exploiting the 4π-collection geometry of the velocity map imaging spectrometer, we not only probe pathways where the efficiency of photoionization is inherently high but also perform PEPICO spectroscopy on relatively weak channels.
Source: Faraday Discussions
DOI: 10.1039/d0fd00120a
Institutions: Indian Institute of Science Education and Research Pune, Tata Institute of Fundamental Research, Max Planck Institute for Nuclear Physics, Think-tank for Action on Social Change, Indian Institute of Technology Hyderabad, Elettra-Sincrotrone Trieste S.C.p.A., Institute of Structure of Matter, Istituto Nazionale di Fisica Nucleare, Laboratori Nazionali di Frascati, National Research Council, Aarhus University, Indian Institute of Technology Madras
Language: English
Subfield: Atomic and Molecular Physics, and Optics
Field: Physics and Astronomy
Domain: Physical Sciences
Open Access status: green
Award: G4940457804
OpenAlex ID: W3118580739
