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dc.contributor.authorHuang, Jen-Hsienen_US
dc.contributor.authorYang, Chuan-Yien_US
dc.contributor.authorHsu, Chih-Yuen_US
dc.contributor.authorChen, Cheng-Lunen_US
dc.contributor.authorLin, Lu-Yinen_US
dc.contributor.authorWang, Rui-Renen_US
dc.contributor.authorHo, Kuo-Chuanen_US
dc.contributor.authorChu, Chih-Weien_US
dc.date.accessioned2014-12-08T15:08:10Z-
dc.date.available2014-12-08T15:08:10Z-
dc.date.issued2009-12-01en_US
dc.identifier.issn1944-8244en_US
dc.identifier.urihttp://dx.doi.org/10.1021/am900573qen_US
dc.identifier.urihttp://hdl.handle.net/11536/6371-
dc.description.abstractWe have systematically studied the self-organization of poly(3-hexylthiophene) (P3HT), an electrochromic material, upon control of the solvent evaporation race. We characterized these polymer films using atomic force microscopy and X-ray diffraction measurements. Well-ordered P3HT structures were developed after solvent annealing; these highly crystalline structures exhibited enhanced electrochromic contrast and reduced resistance within the film, leading to larger coloration efficiencies and faster switching times. The optical contrast (Delta%T), coloration efficiency, and switching time of the P3HT films increased from 54.2%, 182,6 cm(2) C(-1), and 5.3 s, respectively, prior to solvent annealing to 64.8%, 293.5 cm(2) C(-1), and 3.2 s, respectively, after application of the solvent-annealing conditions.en_US
dc.language.isoen_USen_US
dc.subjectelectrochromicen_US
dc.subjectelectrochemistryen_US
dc.subjectconjugated polymeren_US
dc.subjectpoly(3-hexylthiophene)en_US
dc.subjectsolvent annealingen_US
dc.subjectself-organizationen_US
dc.titleSolvent-Annealing-Induced Self-Organization of Poly(3-hexylthiophene), a High-Performance Electrochromic Materialen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/am900573qen_US
dc.identifier.journalACS APPLIED MATERIALS & INTERFACESen_US
dc.citation.volume1en_US
dc.citation.issue12en_US
dc.citation.spage2821en_US
dc.citation.epage2828en_US
dc.contributor.department光電工程學系zh_TW
dc.contributor.departmentDepartment of Photonicsen_US
dc.identifier.wosnumberWOS:000273005500018-
dc.citation.woscount20-
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