Double-resonance studies of electronically autoionizing states of molecular nitrogen.

Saved in:
Bibliographic Details
Title: Double-resonance studies of electronically autoionizing states of molecular nitrogen.
Authors: Sen, Ananya1 (AUTHOR), Pratt, S. T.1 (AUTHOR) stpratt@anl.gov
Source: Molecular Physics. Nov2019, Vol. 117 Issue 21, p2930-2940. 11p.
Subjects: Rydberg states, Photoelectrons, Absorption spectra, Nitrogen
Geographic Terms: Canada
Abstract: Double-resonance excitation of molecular nitrogen, N2, via selected rotational levels of the , v′ = 0 state has been used to probe the first two bands in the new Ogawa series [M. Ogawa, Can. J. Phys. 42, 1087 (1964)], which lie above the first ionisation threshold of the molecule. These bands are rotationally unresolved in room-temperature and jet-cooled absorption spectra, but the double-resonance technique allows a rotational analysis and first confirmation of the assignment as transitions to n = 4 members of the (A2Πu)ndπ, v Rydberg series. In principle, the probe transition from the , v = 0 level to these Rydberg states corresponds to a two-electron transition, and this aspect of the results is explored. Finally, velocity map imaging allows a determination of the photoelectron branching fractions and angular distributions, providing insight into the electronic autoionisation dynamics. [ABSTRACT FROM AUTHOR]
Copyright of Molecular Physics is the property of Taylor & Francis Ltd and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
Database: Engineering Source
Description
Abstract:Double-resonance excitation of molecular nitrogen, N2, via selected rotational levels of the , v′ = 0 state has been used to probe the first two bands in the new Ogawa series [M. Ogawa, Can. J. Phys. 42, 1087 (1964)], which lie above the first ionisation threshold of the molecule. These bands are rotationally unresolved in room-temperature and jet-cooled absorption spectra, but the double-resonance technique allows a rotational analysis and first confirmation of the assignment as transitions to n = 4 members of the (A2Πu)ndπ, v Rydberg series. In principle, the probe transition from the , v = 0 level to these Rydberg states corresponds to a two-electron transition, and this aspect of the results is explored. Finally, velocity map imaging allows a determination of the photoelectron branching fractions and angular distributions, providing insight into the electronic autoionisation dynamics. [ABSTRACT FROM AUTHOR]
ISSN:00268976
DOI:10.1080/00268976.2018.1544672