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dc.contributor.authorJheng, Jyun-Fongen_US
dc.contributor.authorLai, Yu-Yingen_US
dc.contributor.authorWu, Jhong-Sianen_US
dc.contributor.authorChao, Yi-Hsiangen_US
dc.contributor.authorWang, Chien-Lungen_US
dc.contributor.authorHsu, Chain-Shuen_US
dc.date.accessioned2014-12-08T15:30:39Z-
dc.date.available2014-12-08T15:30:39Z-
dc.date.issued2013-05-07en_US
dc.identifier.issn0935-9648en_US
dc.identifier.urihttp://dx.doi.org/10.1002/adma.201300098en_US
dc.identifier.urihttp://hdl.handle.net/11536/21882-
dc.description.abstractA high organic field-effect transistor mobility (0.29 cm(2)V(-1)s(-1)) and bulk-heterojunction polymer solar cell performance (PCE of 6.82%) have been achieved in a low bandgap alternating copolymer consisting of axisymmetrical structural units, 5,6-difluorobenzo-2,1,3-thiadiazole. Introducing the fluorine substituents enhanced intermolecular interaction and improved the solid-state order, which consequently resulted in the highest device performances among the 2,1,3-thiadiazole-quarterthiophene based alternating copolymers.en_US
dc.language.isoen_USen_US
dc.subjectconjugated polymersen_US
dc.subjectbulk-heterojunction organic photovoltaicsen_US
dc.subjectpolymer field-effect transistorsen_US
dc.subjectorganic electronicsen_US
dc.subjectself-assemblyen_US
dc.titleInfluences of the Non-Covalent Interaction Strength on Reaching High Solid-State Order and Device Performance of a Low Bandgap Polymer with Axisymmetrical Structural Unitsen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/adma.201300098en_US
dc.identifier.journalADVANCED MATERIALSen_US
dc.citation.volume25en_US
dc.citation.issue17en_US
dc.citation.spage2445en_US
dc.citation.epage2451en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000318360700010-
dc.citation.woscount23-
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