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dc.contributor.authorWang, Wei-Chihen_US
dc.contributor.authorChen, Sheng-Yuanen_US
dc.contributor.authorYang, Yaw-Wenen_US
dc.contributor.authorHsu, Chain-Shuen_US
dc.contributor.authorTajima, Keisukeen_US
dc.date.accessioned2020-07-01T05:21:20Z-
dc.date.available2020-07-01T05:21:20Z-
dc.date.issued2020-04-07en_US
dc.identifier.issn2050-7488en_US
dc.identifier.urihttp://dx.doi.org/10.1039/d0ta00030ben_US
dc.identifier.urihttp://hdl.handle.net/11536/154409-
dc.description.abstractA new pi-conjugated polymer based on naphthalenediimide with a branched semifluoroalkyl side chain (FNDIT2) was synthesized and used to change the polymer orientations in thin films. X-ray photoelectron spectroscopy and near-edge X-ray absorption fine structure spectroscopy revealed that FNDIT2 spontaneously forms surface-segregated monolayers in blend films with other pi-conjugated polymers to adopt a preferred face-on orientation, with the pi-plane of the polymer aligned more parallel to the surface. Thermal annealing of the films induced further reorientation of the polymers inside the films closer to the face-on orientation, as shown by two-dimensional grazing-incidence wide-angle X-ray scattering. The induced face-on orientations in the films led to higher charge mobility in the vertical direction. This study provides a general and versatile strategy to control the molecular orientation in thin films and enhance the performance of thin-film organic electronics.en_US
dc.language.isoen_USen_US
dc.titleFace-on reorientation of pi-conjugated polymers in thin films by surface-segregated monolayersen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/d0ta00030ben_US
dc.identifier.journalJOURNAL OF MATERIALS CHEMISTRY Aen_US
dc.citation.volume8en_US
dc.citation.issue13en_US
dc.citation.spage6268en_US
dc.citation.epage6275en_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:000527730400008en_US
dc.citation.woscount0en_US
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