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dc.contributor.authorFiedler, Johannes
dc.contributor.authorBerland, Kristian
dc.contributor.authorBuhmann, Stefan Yoshi
dc.date.accessioned2023-01-17T09:50:54Z
dc.date.available2023-01-17T09:50:54Z
dc.date.created2022-11-06T16:33:16Z
dc.date.issued2022
dc.identifier.issn0021-9606
dc.identifier.urihttps://hdl.handle.net/11250/3043898
dc.description.abstractWe study the impact of an environment on the electromagnetic responses of a molecule in the presence of a dielectric medium. By applying the dipole–dipole coupling between the molecule’s and the environment’s degrees of freedom, we can reduce the complex system into its components and predict excitation lifetimes of single and few molecules attached to a dielectric surface by knowing the entire quantum–mechanical properties of the molecules, such as transition energies and dipole moments. The derived theory allows for the description of superradiance between two molecules depending on the geometric arrangement between both concerning their separation and orientation with respect to each other. We analyze the possibility of superradiance between two molecules bound to a dielectric sphere and determine a change in the relevant length scale where the usually considered wavelength in free space is replaced with the binding distance, drastically reducing the length scales at which collective effects can take place.en_US
dc.language.isoengen_US
dc.publisherAIPen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titlePurcell-induced suppression of superradiance for molecular overlayers on noble atom surfacesen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2022 The Author(s)en_US
dc.source.articlenumber194111en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1063/5.0106503
dc.identifier.cristin2069621
dc.source.journalJournal of Chemical Physicsen_US
dc.relation.projectSigma2: NN9650Ken_US
dc.identifier.citationJournal of Chemical Physics. 2022, 157 (19), 194111.en_US
dc.source.volume157en_US
dc.source.issue19en_US


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