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dc.contributor.authorMineo, Hirobumien_US
dc.contributor.authorFujimura, Yuichien_US
dc.date.accessioned2018-08-21T05:54:01Z-
dc.date.available2018-08-21T05:54:01Z-
dc.date.issued2017-05-04en_US
dc.identifier.issn1948-7185en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.jpclett.7b00704en_US
dc.identifier.urihttp://hdl.handle.net/11536/145478-
dc.description.abstractControl of pi-electrons in polycyclic aromatic hydrocarbons (PAHs) is one of the fundamental issues in optoelectronics for ultrafast optical switching devices. We have proposed an effective scenario for design of the generation of coherent ring currents in naphthalene (D-2h), which is the smallest, unit of planar PAHs. It has been demonstrated by using quantum chemical calculations and quantum optimal control (QOC) simulations that two types of ring currents, parallel and antiparallel, can be generated by resonance excitations by two linearly polarized lasers. A parallel (antiparallel) ring current means that the currents of two benzene rings run in the same (opposite) directions. The two types of ring currents may be experimentally identified by magnetic force microscopy. The QOC simulations indicate that a parallel ring current can be generated by using continuous wave and Gaussian pulse lasers with their time delay without relying on a sophisticated experimental apparatus. The present results provide a guiding principle of coherent it-electronics in PAHs for next-generation organic optical switching devices.en_US
dc.language.isoen_USen_US
dc.titleQuantum Design of pi-Electron Ring Currents in Polycyclic Aromatic Hydrocarbons: Parallel and Antiparallel Ring Currents in Naphthaleneen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/acs.jpclett.7b00704en_US
dc.identifier.journalJOURNAL OF PHYSICAL CHEMISTRY LETTERSen_US
dc.citation.volume8en_US
dc.citation.spage2019en_US
dc.citation.epage2025en_US
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000400885600016en_US
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