| DC 欄位 |
值 |
語言 |
| DC.contributor | 化學學系 | zh_TW |
| DC.creator | 葉佳明 | zh_TW |
| DC.creator | Chia-Ming Yeh | en_US |
| dc.date.accessioned | 2011-7-20T07:39:07Z | |
| dc.date.available | 2011-7-20T07:39:07Z | |
| dc.date.issued | 2011 | |
| dc.identifier.uri | http://ir.lib.ncu.edu.tw:88/thesis/view_etd.asp?URN=982203058 | |
| dc.contributor.department | 化學學系 | zh_TW |
| DC.description | 國立中央大學 | zh_TW |
| DC.description | National Central University | en_US |
| dc.description.abstract | 利用“one-pot” reaction 開發出不對稱主體苯三併環噻吩 (11)，其衍生物分子 (1) & (2) 已成功製備，兩者皆為 p-type 有機半導體材料，載子移動率利用真空蒸鍍製備分別達 0.026 及 9x10-4 cm2/Vs。可溶性聯噻吩主體的產率已順利提升，其衍生物 (3) ~ (9) 亦已成功開發，其中可溶性分子 (6)、(7)、(8) 皆展現不錯的載子移動率達 0.15、0.38 及 0.24 cm2/Vs。這些有機半導體材料皆表現相當良好的光、空氣與熱穩定性。
| zh_TW |
| dc.description.abstract | Asymmetric fused thiophene compound (11) was synthesized by “one-pot” reaction. Based on compound (11), derivatives (1) and (2) have been developed. Both compounds exhibit p-type field-effect performances with mobility of 0.026 and 9x10-4 cm2/Vs via vacuum evaporation, respectively.
Compounds (3) ~ (9) have been successfully developed based on bithiophene compound (18). Preparation of soluble compound (18) has been improved with better yield. Compounds (6), (7), and (8) exhibit good field-effect performances with high mobility of 0.15, 0.38, and 0.24 cm2/Vs via solution process, respectively. All of these new semiconductor materials exhibit good stability under light, air, and thermal conditions.
| en_US |
| DC.subject | 有機薄膜電晶體 | zh_TW |
| DC.subject | 可溶性 | zh_TW |
| DC.subject | organic thin film transistor | en_US |
| DC.title | 有機薄膜電晶體材料苯三併環噻吩及可溶性聯噻吩衍生物之開發 | zh_TW |
| dc.language.iso | zh-TW | zh-TW |
| DC.title | Synthesis of Soluble Organic Thin film transistors. | en_US |
| DC.type | 博碩士論文 | zh_TW |
| DC.type | thesis | en_US |
| DC.publisher | National Central University | en_US |