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dc.contributor.authorZhong, X
dc.contributor.authorChervy, T
dc.contributor.authorZhang, L
dc.contributor.authorThomas, A
dc.contributor.authorGeorge, J
dc.contributor.authorGenet, C
dc.contributor.authorHutchison, JA
dc.contributor.authorEbbesen, TW
dc.date.accessioned2021-02-04T02:05:45Z
dc.date.available2021-02-04T02:05:45Z
dc.date.issued2017-07-24
dc.identifier.citationZhong, X., Chervy, T., Zhang, L., Thomas, A., George, J., Genet, C., Hutchison, J. A. & Ebbesen, T. W. (2017). Energy Transfer between Spatially Separated Entangled Molecules. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 56 (31), pp.9034-9038. https://doi.org/10.1002/anie.201703539.
dc.identifier.issn1433-7851
dc.identifier.urihttp://hdl.handle.net/11343/259570
dc.description.abstractLight-matter strong coupling allows for the possibility of entangling the wave functions of different molecules through the light field. We hereby present direct evidence of non-radiative energy transfer well beyond the Förster limit for spatially separated donor and acceptor cyanine dyes strongly coupled to a cavity. The transient dynamics and the static spectra show an energy transfer efficiency approaching 37 % for donor-acceptor distances ≥100 nm. In such systems, the energy transfer process becomes independent of distance as long as the coupling strength is maintained. This is consistent with the entangled and delocalized nature of the polaritonic states.
dc.languageEnglish
dc.publisherWILEY-V C H VERLAG GMBH
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0
dc.titleEnergy Transfer between Spatially Separated Entangled Molecules
dc.typeJournal Article
dc.identifier.doi10.1002/anie.201703539
melbourne.affiliation.departmentSchool of Chemistry
melbourne.affiliation.facultyScience
melbourne.source.titleAngewandte Chemie International Edition
melbourne.source.volume56
melbourne.source.issue31
melbourne.source.pages9034-9038
dc.rights.licenseCC BY-NC
melbourne.elementsid1215860
melbourne.contributor.authorHutchison, James
dc.identifier.eissn1521-3773
melbourne.accessrightsOpen Access


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