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dc.contributor.authorLi, Jieen_US
dc.contributor.authorUeno, Koseien_US
dc.contributor.authorUehara, Hiyorien_US
dc.contributor.authorGuo, Jingchunen_US
dc.contributor.authorOshikiri, Tomoyaen_US
dc.contributor.authorMisawa, Hiroakien_US
dc.date.accessioned2017-04-21T06:55:44Z-
dc.date.available2017-04-21T06:55:44Z-
dc.date.issued2016-07-21en_US
dc.identifier.issn1948-7185en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.jpclett.6b01224en_US
dc.identifier.urihttp://hdl.handle.net/11536/134133-
dc.description.abstractWe report on the spectral properties of strong coupling between the localized surface plasmon resonances (LSPRs) of aluminum (Al) nanostructures and tetraphenylporphyrin tetrasulfonic acid hydrate (TPPS) J-aggregates. Because of their wide spectral range of LSPR bands from ultraviolet to near-infrared wavelengths by controlling structural size, Al nanodisks can realize strong coupling with different excitons of TPPS J-aggregates. The Rabi splitting energies of the excitons based on Soret and Qbands are 300 and 180 meV, respectively. In addition to extinction spectrum, we have also measured an excitation spectrum to determine the essential absorption of the hybrid states and successfully confirmed a shoulder peak corresponding to a lower branch of hybrid states. In Al nanorod systems, strong coupling with two excitons can also be selectively induced by merely rotating the polarization of the incident light, which constituted a simple platform for the dynamic control of exciton/plasmon coupling states.en_US
dc.language.isoen_USen_US
dc.titleDual Strong Couplings Between TPPS J-Aggregates and Aluminum Plasmonic Statesen_US
dc.identifier.doi10.1021/acs.jpclett.6b01224en_US
dc.identifier.journalJOURNAL OF PHYSICAL CHEMISTRY LETTERSen_US
dc.citation.volume7en_US
dc.citation.issue14en_US
dc.citation.spage2786en_US
dc.citation.epage2791en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000380415400024en_US
Appears in Collections:Articles