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...

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Main Authors: Peng Sheng, 陳鵬生
Other Authors: Ming-Chou Chen
Format: Others
Language:zh-TW
Published: 2011
Online Access:http://ndltd.ncl.edu.tw/handle/87264080598597958563
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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
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language zh-TW
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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
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