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Single-photon core-valence double ionization of molecular oxygen
KTH, Skolan för bioteknologi (BIO), Teoretisk kemi (stängd 20110512).
Vise andre og tillknytning
2008 (engelsk)Inngår i: Physical Review A. Atomic, Molecular, and Optical Physics, ISSN 1050-2947, E-ISSN 1094-1622, Vol. 78, nr 2, s. 023409-Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Single-photon core-valence double ionization of molecular oxygen has been studied using a magnetic bottle time-of-flight electron coincidence spectrometer. The K-1 V-1 double ionization electron spectrum of O2 is reported and is assigned with the aid of ab initio calculations. A direct comparison of the core-valence double ionization electron spectra with the conventional valence band photoelectron spectrum is made. The lowest core-valence double ionization energy is found to be 571.6 eV and is associated with a Π3 dicationic state.

sted, utgiver, år, opplag, sider
2008. Vol. 78, nr 2, s. 023409-
Emneord [en]
Electrons, Ionization, Nonmetals, Oxygen, Photoelectron spectroscopy, Photoionization, Photons
HSV kategori
Identifikatorer
URN: urn:nbn:se:kth:diva-9417DOI: 10.1103/PhysRevA.78.023409ISI: 000259263500009Scopus ID: 2-s2.0-50049133229OAI: oai:DiVA.org:kth-9417DiVA, id: diva2:113893
Merknad
QC 20100929Tilgjengelig fra: 2008-10-31 Laget: 2008-10-31 Sist oppdatert: 2017-12-14bibliografisk kontrollert
Inngår i avhandling
1. Quantum mechanical studies of ionization and electron transfer in diatomic systems: O2 and H+ + H-
Åpne denne publikasjonen i ny fane eller vindu >>Quantum mechanical studies of ionization and electron transfer in diatomic systems: O2 and H+ + H-
2008 (engelsk)Licentiatavhandling, med artikler (Annet vitenskapelig)
Abstract [en]

 

The present thesis is based upon two papers concerning the core-valence double onization of molecular oxygen and mutual neutralization of H+ and H- ions at low collision energies.

The former of these processes has been studied for the first time using a magnetic bottle time-of-ight electron coincidence spectrometer in combination with ab initio electronic structure calculations. The core-valence photoelectron spectra have been interpreted by comparing with the calculated double ionization energies, as well as the conventional valence band spectrum. Based on this comparison, some general features of the process are discussed and assignments for several of the dicationic states proposed.

The latter process has been studied by means of a molecular close coupling approach in which both the nuclei and the electrons have been treated at a quantum mechanical level of theory. Accurate ab initio potential energy curves and non-adiabatic couplings have been used to calculate the neutralization cross section in the collision energy region 0.001 to 100 eV. Special emphasis has been put on the energy region below a few eV from which the low temperature rate coe_cient is evaluated. In this region, the calculated neutralization cross section is in good agreement with several other theoretical studies, but is a factor of two to three lower than the only published experimental data.

 

sted, utgiver, år, opplag, sider
Stockholm: KTH, 2008. s. viii, 37
Serie
Trita-BIO-Report, ISSN 1654-2312 ; 2008:21
HSV kategori
Identifikatorer
urn:nbn:se:kth:diva-9419 (URN)978-91-7415-147-3 (ISBN)
Presentation
2008-10-31, FB42, AlbaNova, Stockholm, 13:00 (engelsk)
Veileder
Merknad
QC 20101123Tilgjengelig fra: 2008-11-04 Laget: 2008-10-31 Sist oppdatert: 2010-11-23bibliografisk kontrollert

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