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Selective negative-ion formation from core-valence doubly excited states of the water molecule
Malmö University, Faculty of Technology and Society (TS), Department of Materials Science and Applied Mathematics (MTM). MAX IV Laboratory, Lund University, P.O. Box 118, Lund, 22100, Sweden.ORCID iD: 0000-0002-7985-8741
Optoelectronics Research Centre, University of Southampton, Highfield Campus, G-Hampshire, SO17 1BJ, United Kingdom; MAX IV Laboratory, Lund University, P.O. Box 118, Lund, 22100, Sweden.
Department of Physics, Stockholm University, AlbaNova University Center, Stockholm, 10691, Sweden.
Department of Physics, Stockholm University, AlbaNova University Center, Stockholm, 10691, Sweden.
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2018 (English)In: Physical Review A: covering atomic, molecular, and optical physics and quantum information, ISSN 2469-9926, E-ISSN 2469-9934, Vol. 98, no 5, article id 053432Article in journal (Refereed) Published
Abstract [en]

This study focuses on the role of negative-ion formation in the decay of core-valence doubly excited water molecules. Combining negative- and positive-ion coincidence measurements with calculated energies of core-valence doubly excited states, we find that O− and H− production is enhanced selectively. In particular, we suggest that O− production is correlated to double occupancy of the antibonding 4a1 virtual orbital, while H− appears at electronic states with double occupancy in 2b2. We also show that H− and O− can be created as a result of electron recapture close to the O 1s ionization potential.

Place, publisher, year, edition, pages
American Physical Society, 2018. Vol. 98, no 5, article id 053432
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Natural Sciences
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URN: urn:nbn:se:mau:diva-15983DOI: 10.1103/PhysRevA.98.053432ISI: 000451329500027Scopus ID: 2-s2.0-85057522237Local ID: 27298OAI: oai:DiVA.org:mau-15983DiVA, id: diva2:1419505
Available from: 2020-03-30 Created: 2020-03-30 Last updated: 2024-06-17Bibliographically approved

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Publisher's full textScopushttps://journals.aps.org/pra/abstract/10.1103/PhysRevA.98.053432

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Stråhlman, Christian

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