Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7738
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dc.contributor.authorLaForge, A. C.en_US
dc.contributor.authorMANDAL, S. et al.en_US
dc.date.accessioned2023-04-21T09:28:52Z-
dc.date.available2023-04-21T09:28:52Z-
dc.date.issued2022-12en_US
dc.identifier.citationPhysical Chemistry Chemical Physics, 24(47), 28844-28852.en_US
dc.identifier.issn1463-9076en_US
dc.identifier.issn1463-9084en_US
dc.identifier.urihttps://doi.org/10.1039/D2CP03335Fen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7738-
dc.description.abstractSuperfluid helium nanodroplets are often considered as transparent and chemically inert nanometer-sized cryo-matrices for high-resolution or time-resolved spectroscopy of embedded molecules and clusters. On the other hand, when the helium nanodroplets are resonantly excited with XUV radiation, a multitude of ultrafast processes are initiated, such as relaxation into metastable states, formation of nanoscopic bubbles or excimers, and autoionization channels generating low-energy free electrons. Here, we discuss the full spectrum of ultrafast relaxation processes observed when helium nanodroplets are electronically excited. In particular, we perform an in-depth study of the relaxation dynamics occurring in the lowest 1s2s and 1s2p droplet bands using high resolution, time-resolved photoelectron spectroscopy. The simplified excitation scheme and improved resolution allow us to identify the relaxation into metastable triplet and excimer states even when exciting below the droplets' autoionization threshold, unobserved in previous studies.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectLiquid-heliumen_US
dc.subjectClustersen_US
dc.subjectElectronen_US
dc.subjectStatesen_US
dc.subjectHEen_US
dc.subjectExcitationsen_US
dc.subjectMoleculesen_US
dc.subjectDropletsen_US
dc.subjectAtomsen_US
dc.subjectPureen_US
dc.subject2022en_US
dc.titleRelaxation dynamics in excited helium nanodroplets probed with high resolution, time-resolved photoelectron spectroscopyen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitlePhysical Chemistry Chemical Physicsen_US
dc.publication.originofpublisherForeignen_US
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