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dc.contributor.authorCheng, An-Chiehen_US
dc.contributor.authorNiinomi, Hiromasaen_US
dc.contributor.authorOmatsu, Takashigeen_US
dc.contributor.authorIshida, Shutaroen_US
dc.contributor.authorSasaki, Keijien_US
dc.contributor.authorSugiyama, Terukien_US
dc.date.accessioned2020-07-01T05:22:06Z-
dc.date.available2020-07-01T05:22:06Z-
dc.date.issued2020-06-04en_US
dc.identifier.issn1948-7185en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.jpclett.0c01041en_US
dc.identifier.urihttp://hdl.handle.net/11536/154518-
dc.description.abstractPlasmonic manipulation using well-designed triangular trimeric gold nanostructures achieves a giant (greater than 50%) crystal enantiomeric excess (CEE) of sodium chlorate (NaClO3). Stronger asymmetric interactions between molecule and light are pursued to reach high enantiomeric excess. The well-designed gold nanostructures immersed in a saturated NaClO3 D2O solution were irradiated with linear, left-hand, and right-hand circular polarizations of a 1064 nm continuous-wave laser. Within seconds of the start of the irradiation, an achiral metastable crystal was formed at the laser focus, and further irradiation induced a subsequent polymorphic transition to the chiral crystal. The crystal chirality is sensitive to the handedness of circular polarization, allowing for efficient enantioselectivity. The mechanisms to achieve this giant CEE are proposed based on the results of electromagnetic field analysis generated near the nanostructure by the finite element method.en_US
dc.language.isoen_USen_US
dc.titlePlasmonic Manipulation-Controlled Chiral Crystallization of Sodium Chlorateen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/acs.jpclett.0c01041en_US
dc.identifier.journalJOURNAL OF PHYSICAL CHEMISTRY LETTERSen_US
dc.citation.volume11en_US
dc.citation.issue11en_US
dc.citation.spage4422en_US
dc.citation.epage4426en_US
dc.contributor.department交大名義發表zh_TW
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentNational Chiao Tung Universityen_US
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000538759600028en_US
dc.citation.woscount0en_US
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