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dc.contributor.authorBaraclough, M
dc.contributor.authorSeetharaman, SS
dc.contributor.authorHooper, IR
dc.contributor.authorBarnes, WL
dc.date.accessioned2020-01-31T13:43:29Z
dc.date.issued2019-11-20
dc.description.abstractMolecular aggregates are a fascinating and important class of materials, particularly in the context of optical (pigmented) materials. In nature, molecular aggregates are employed in photosynthetic light harvesting structures, while synthetic aggregates are employed in new generation molecular sensors and magnets. The roles of disorder and symmetry are vital in determining the photophysical properties of molecular aggregates, but have been hard to investigate experimentally, owing to a lack of sufficient structural control at the molecular level and the challenge of probing their optical response with molecular spatial resolution. We present a new approach using microwave analogues of molecular aggregates to study the properties of both individual meta-molecules and 1D molecular chains. We successfully replicate J- and H-aggregate behavior and demonstrate the power of our approach through the controlled introduction of structural symmetry breaking. Our results open a new area of study, combining concepts from molecular science and metamaterials.en_GB
dc.description.sponsorshipEngineering and Physical Sciences Research Council (EPSRC)en_GB
dc.description.sponsorshipQinetiQ Ltden_GB
dc.description.sponsorshipEuropean Research Councilen_GB
dc.identifier.citationVol. 6, pp. 3003 - 3009en_GB
dc.identifier.doi10.1021/acsphotonics.9b01208
dc.identifier.grantnumberEP/L015331/1en_GB
dc.identifier.grantnumberERC-2016-AdG-742222en_GB
dc.identifier.urihttp://hdl.handle.net/10871/40676
dc.language.isoenen_GB
dc.publisherAmerican Chemical Societyen_GB
dc.rights.embargoreasonUnder embargo until 25 October 2020 in compliance with publisher policyen_GB
dc.rights© The Author(s). Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. en_GB
dc.subjectmolecular aggregateen_GB
dc.subjectmetamaterialen_GB
dc.subjectdipole-dipole interactionen_GB
dc.titleMetamaterial analogues of molecular aggregatesen_GB
dc.typeArticleen_GB
dc.date.available2020-01-31T13:43:29Z
dc.descriptionThis is the author accepted manuscripten_GB
dc.identifier.eissn2330-4022
dc.identifier.journalACS Photonicsen_GB
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2019-10-25
exeter.funder::Engineering and Physical Sciences Research Council (EPSRC)en_GB
exeter.funder::Engineering and Physical Sciences Research Council (EPSRC)en_GB
exeter.funder::QinetiQ Ltden_GB
rioxxterms.versionAMen_GB
rioxxterms.licenseref.startdate2019-10-25
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2020-01-31T13:34:56Z
refterms.versionFCDAM
refterms.dateFOA2020-10-24T23:00:00Z
refterms.panelBen_GB


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© The Author(s). Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 
Except where otherwise noted, this item's licence is described as © The Author(s). Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.