Opto-electronics of non-fully conjugated molecules was demonstrated successfully in this research as light emitting diodes (LEDs). A series of benzoxazole poly[2,2-(m-2-hydroxyl phenylene)-4-4¡¦-hexafluoroisopro- pane-bibenzoxazoles] (6F-PBO-OH, Am) and benzimidazole poly[2,2¡¦- (2-hydroxy-o-phenylene)-5,5¡¦-bibenzimiazole] (OH-Pbi, B(1-m)) were copolymerized for coil-like non-fully conjugated poly-(Am-co-B(1-m)) for luminescence investigation.
UV-Vis absorption of the non-fully conjugated copolymers showed superposition of individual absorption response from the two chemical components of the copolymer. However, the photoluminescence (PL) and the electroluminescence (EL) emissions had a red shift with increasing OH-Pbi content. It seemed to suggest that OH-Pbi was more charge delocalized than 6F-PBO-OH. In mono-layer LEDs, the diode threshold voltages were about at 2 ~ 3 V and the EL showed a green emission. Tunable emission was not observed in varying the m value of the copolymers.
Composites of copolymer, poly(Am-co-B(1-m)) and multi-wall carbon nanotube (MWNT) were in-situ synthesized for mono-layer LED fabrication. Few MWNT aggregation was observed via the field-emission scanning electron microscopy. It was a success in dispersing MWNT in the copolymers. There was a red shift with MWNT addition in the PL and the EL emissions. The diode threshold voltages were about at 2 ~ 5 V and the EL emission still showed a green emission. According to this study, MWNT was inconsequential on the PL and the EL emissions of the copolymers up to 2 wt. %.
Identifer | oai:union.ndltd.org:NSYSU/oai:NSYSU:etd-0708104-113702 |
Date | 08 July 2004 |
Creators | Hsu, Yi-long |
Contributors | Jui-Hung Hsu, Shin-Jung Bai, Bae-Heng Tseng |
Publisher | NSYSU |
Source Sets | NSYSU Electronic Thesis and Dissertation Archive |
Language | English |
Detected Language | English |
Type | text |
Format | application/pdf |
Source | http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708104-113702 |
Rights | not_available, Copyright information available at source archive |
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