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dc.contributor.authorZhang, Haichangen_US
dc.contributor.authorZhang, Shuoen_US
dc.contributor.authorMao, Yifanen_US
dc.contributor.authorLiu, Keweien_US
dc.contributor.authorChen, Yu-Mingen_US
dc.contributor.authorJiang, Zhangen_US
dc.contributor.authorStrzalka, Josephen_US
dc.contributor.authorYang, Wenjunen_US
dc.contributor.authorWang, Chien-Lungen_US
dc.contributor.authorZhu, Yuen_US
dc.date.accessioned2018-08-21T05:54:05Z-
dc.date.available2018-08-21T05:54:05Z-
dc.date.issued2017-06-07en_US
dc.identifier.issn1759-9954en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c7py00616ken_US
dc.identifier.urihttp://hdl.handle.net/11536/145567-
dc.description.abstractTwo novel donor-acceptor pi-conjugated polymers based on naphthodipyrrolidone (NDP) were synthesized and characterized. The polymers possess low band gaps and suitable molecular orbital levels as ambipolar semiconductors. The thin film organic field effect transistor of NDP polymers exhibited ambipolar transport properties with a high electron mobility up to 0.67 cm(2) V-1 s(-1). The grazing-incidence wide-angle X-ray scattering (GIWAXS) studies demonstrated that the polymer molecules pack into a long-range-ordered lamellar structure with isotropically oriented crystalline domains. Thermal annealing promoted edge-on lamellar stacking as evidenced by the increased diffraction intensity along the out-of-plane direction. The polymer with NDP and bithiophene units achieved the best edge-on lamellar stacking after thermal annealing, which yielded the best electron transport performance in this work.en_US
dc.language.isoen_USen_US
dc.titleNaphthodipyrrolidone (NDP) based conjugated polymers with high electron mobility and ambipolar transport propertiesen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c7py00616ken_US
dc.identifier.journalPOLYMER CHEMISTRYen_US
dc.citation.volume8en_US
dc.citation.spage3255en_US
dc.citation.epage3260en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000402300400002en_US
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