Attosecond photoionization delays in the vicinity of molecular Feshbach resonances

Author:

Borràs Vicent J.1ORCID,González-Vázquez Jesús12ORCID,Argenti Luca3,Martín Fernando145ORCID

Affiliation:

1. Departamento de Química, Módulo 13, Universidad Autónoma de Madrid, 28049 Madrid, Spain.

2. Institute for Advanced Research in Chemical Sciences (IAdChem), Universidad Autónoma de Madrid, 28049 Madrid, Spain.

3. Department of Physics and CREOL, University of Central Florida, Orlando, FL 32186, USA.

4. Instituto Madrileño de Estudios Avanzados en Nanociencia (IMDEA Nano), Cantoblanco, 28049 Madrid, Spain.

5. Condensed Matter Physics Center (IFIMAC), Universidad Autónoma de Madrid, 28049 Madrid, Spain.

Abstract

Temporal delays extracted from photoionization phases are currently determined with attosecond resolution by using interferometric methods. Such methods require special care when photoionization occurs near Feshbach resonances due to the interference between direct ionization and autoionization. Although theory can accurately handle these interferences in atoms, in molecules, it has to face an additional, so far insurmountable problem: Autoionization is slow, and nuclei move substantially while it happens, i.e., electronic and nuclear motions are coupled. Here, we present a theoretical framework to account for this effect and apply it to evaluate time-resolved and vibrationally resolved photoelectron spectra and photoionization phases of N 2 irradiated by a combination of an extreme ultraviolet (XUV) attosecond pulse train and an infrared pulse. We show that Feshbach resonances lead to unusual non–Franck-Condon vibrational progressions and to ionization phases that strongly vary with photoelectron energy irrespective of the vibrational state of the remaining molecular cation.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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