完整後設資料紀錄
DC 欄位語言
dc.contributor.authorLu, Fang-Hsienen_US
dc.contributor.authorMohamed, Mohamed Gamalen_US
dc.contributor.authorLiu, Tzeng-Fengen_US
dc.contributor.authorChao, Chuen-Guangen_US
dc.contributor.authorKuo, Shiao-Weien_US
dc.date.accessioned2019-04-03T06:36:22Z-
dc.date.available2019-04-03T06:36:22Z-
dc.date.issued2015-01-01en_US
dc.identifier.issn2046-2069en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c5ra18751fen_US
dc.identifier.urihttp://hdl.handle.net/11536/128454-
dc.description.abstractSemi-crystalline CuCl2(ethylene glycol)/poly(3-hexylthiophene) complexes (CE-P3HT) with specific textures and self-assembled structures can be fabricated using a facile co-solvent/chelation method. The morphologies and self-assembled structures of these CE-P3HT complexes were dependent on the concentration of CuCl2(ethylene glycol) (CuCl(2)EG) in solution. Transmission electron microscopy (TEM) revealed the CE-P3HT sample comprising EG and numerous CuCl2/P3HT dots (C-P3HT dots) that originated from the P3HT main chains interacting with CuCl2 crystals; the average size of this C-P3HT dots was ca. 20 nm. Prior to formation of the solid state of CE-P3HT structures, the CE-P3HT complex in solution displayed a novel phenomenon: a specific luminescence property with an absorption energy gap of 3.71-4.46 eV. This quantum effect resulted from the chelates formed between the Cu2+ ions and the thioether units of the conjugated P3HT polymer.en_US
dc.language.isoen_USen_US
dc.titleA facile cosolvent/chelation method for the preparation of semi-crystalline CuCl2(ethylene glycol)/poly(3-hexylthiophene) complexes displaying specific luminescence propertiesen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c5ra18751fen_US
dc.identifier.journalRSC ADVANCESen_US
dc.citation.volume5en_US
dc.citation.issue106en_US
dc.citation.spage87723en_US
dc.citation.epage87729en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000363233500099en_US
dc.citation.woscount0en_US
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