Experimental study of laser-induced isomerization dynamics of specific C2H2q ions

dc.citation.doi10.1103/PhysRevA.101.013406
dc.citation.issn2469-9926
dc.citation.issue1
dc.citation.jtitlePhysical Review A
dc.citation.volume101
dc.contributor.authorJochim, Bethany
dc.contributor.authorZohrabi, M.
dc.contributor.authorSevert, T.
dc.contributor.authorBerry, Ben
dc.contributor.authorBetsch, K. J.
dc.contributor.authorFeizollah, Peyman
dc.contributor.authorRajput, Jyoti
dc.contributor.authorWells, E.
dc.contributor.authorCarnes, K. D.
dc.contributor.authorBen-Itzhak, I.
dc.date.accessioned2023-12-07T22:39:30Z
dc.date.available2023-12-07T22:39:30Z
dc.date.issued2020-01-08
dc.date.published2020-01-08
dc.description.abstractWe investigate intense, ultrafast laser-induced isomerization and two-body fragmentation of acetylene monocations and dications using coincidence three-dimensional momentum imaging. Whereas the vast majority of previous work on strong-field isomerization and fragmentation of acetylene has necessarily involved ionization, by focusing solely on dissociation of ion-beam targets, we ensure that the dynamics ensue within a single molecular ion species, potentially simplifying interpretation. We demonstrate the rich information that can be extracted from such a measurement and discuss advantages and disadvantages of this approach.
dc.identifier.urihttps://hdl.handle.net/2097/44057
dc.relation.urihttps://link.aps.org/doi/10.1103/PhysRevA.101.013406
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dc.titleExperimental study of laser-induced isomerization dynamics of specific C2H2q ions
dc.typeText

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