Synthesis of Organic Semiconductor Materials
碩士 === 國立中央大學 === 化學研究所 === 99 === This article focuses on the development of highly stable materials for organic semiconductors. Three soluble compounds (1), (3), and (6) were synthesized. Extension of π-π conjugation and introduction of electron withdrawing group to the fused thiophene core, n-typ...
Main Authors: | , |
---|---|
Other Authors: | |
Format: | Others |
Language: | zh-TW |
Published: |
2011
|
Online Access: | http://ndltd.ncl.edu.tw/handle/87264080598597958563 |
id |
ndltd-TW-099NCU05065086 |
---|---|
record_format |
oai_dc |
spelling |
ndltd-TW-099NCU050650862017-07-07T04:31:06Z http://ndltd.ncl.edu.tw/handle/87264080598597958563 Synthesis of Organic Semiconductor Materials 有機薄膜電晶體材料三併環及四併環噻吩衍生物之開發 Peng Sheng 陳鵬生 碩士 國立中央大學 化學研究所 99 This article focuses on the development of highly stable materials for organic semiconductors. Three soluble compounds (1), (3), and (6) were synthesized. Extension of π-π conjugation and introduction of electron withdrawing group to the fused thiophene core, n-type compounds (2), (3), (4), and (7) were developed. Asymmetric fused thiophene compounds (8) and (9) as well as a symmetric compound (10) were also prepared.The OTFT devices are fabricated by two groups:Tobin J. Marks group at Northwestern University (vacuum deposition) and Industrial Technology Research Institute (solution process).Compounds (2) and (4) exhibit n-channel mobility of 0.33 and 0.37 cm2/Vs with vacuum deposition, respectively. Compounds (5) and (6) exhibit n-channel mobility of 0.08 and 0.15 cm2/Vs via solution process. Compounds (8), (9), and (10) show p-channel mobility of 0.23 cm2/Vs,7.28×10-3 cm2/Vs as well as 0.049 cm2/Vs。 Ming-Chou Chen 陳銘洲 2011 學位論文 ; thesis 171 zh-TW |
collection |
NDLTD |
language |
zh-TW |
format |
Others
|
sources |
NDLTD |
description |
碩士 === 國立中央大學 === 化學研究所 === 99 === This article focuses on the development of highly stable materials for organic semiconductors. Three soluble compounds (1), (3), and (6) were synthesized. Extension of π-π conjugation and introduction of electron withdrawing group to the fused thiophene core, n-type compounds (2), (3), (4), and (7) were developed. Asymmetric fused
thiophene compounds (8) and (9) as well as a symmetric compound (10) were also prepared.The OTFT devices are fabricated by two groups:Tobin J. Marks group at Northwestern University (vacuum deposition)
and Industrial Technology Research Institute (solution process).Compounds (2) and (4) exhibit n-channel mobility of 0.33 and 0.37 cm2/Vs with vacuum deposition, respectively. Compounds (5) and (6) exhibit n-channel mobility of 0.08 and 0.15 cm2/Vs via solution process.
Compounds (8), (9), and (10) show p-channel mobility of 0.23 cm2/Vs,7.28×10-3 cm2/Vs as well as 0.049 cm2/Vs。
|
author2 |
Ming-Chou Chen |
author_facet |
Ming-Chou Chen Peng Sheng 陳鵬生 |
author |
Peng Sheng 陳鵬生 |
spellingShingle |
Peng Sheng 陳鵬生 Synthesis of Organic Semiconductor Materials |
author_sort |
Peng Sheng |
title |
Synthesis of Organic Semiconductor Materials |
title_short |
Synthesis of Organic Semiconductor Materials |
title_full |
Synthesis of Organic Semiconductor Materials |
title_fullStr |
Synthesis of Organic Semiconductor Materials |
title_full_unstemmed |
Synthesis of Organic Semiconductor Materials |
title_sort |
synthesis of organic semiconductor materials |
publishDate |
2011 |
url |
http://ndltd.ncl.edu.tw/handle/87264080598597958563 |
work_keys_str_mv |
AT pengsheng synthesisoforganicsemiconductormaterials AT chénpéngshēng synthesisoforganicsemiconductormaterials AT pengsheng yǒujībáomódiànjīngtǐcáiliàosānbìnghuánjísìbìnghuánsāifēnyǎnshēngwùzhīkāifā AT chénpéngshēng yǒujībáomódiànjīngtǐcáiliàosānbìnghuánjísìbìnghuánsāifēnyǎnshēngwùzhīkāifā |
_version_ |
1718492126269931520 |