Synthesis and Characterization of Conjugated Polymers Based on Two Dimensional 5,6-Difluoro-benzo-2,1,3-thiadiazole with Thiophene Units and Silolobis(selenophene) Based Conjugated Polymers
碩士 === 國立交通大學 === 應用化學系碩博士班 === 104 === In this study, two series of conjugated polymers were synthesized for the application of organic thin film transistors (OTETs) and organic solar cells (OSCs). For the first series, perylene and dithienylbenzothiadiazole (DTBT) were introduced to the side chai...
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ndltd-TW-104NCTU55000022019-05-15T22:34:02Z http://ndltd.ncl.edu.tw/handle/fs8kmm Synthesis and Characterization of Conjugated Polymers Based on Two Dimensional 5,6-Difluoro-benzo-2,1,3-thiadiazole with Thiophene Units and Silolobis(selenophene) Based Conjugated Polymers 含二維側鏈之5,6-雙氟-2,1,3-苯并噻二唑與噻吩之共軛高分子及矽雜環戊二烯并二硒吩之共軛高分子之合成與鑑定 Yang, Cheng-Tai 楊鎮臺 碩士 國立交通大學 應用化學系碩博士班 104 In this study, two series of conjugated polymers were synthesized for the application of organic thin film transistors (OTETs) and organic solar cells (OSCs). For the first series, perylene and dithienylbenzothiadiazole (DTBT) were introduced to the side chain of poly(5,6-difluoro-benzo-2,1,3-thiadiazole co-quaterthiophene) (PTh4FBT) to obtain two types of copolymers, i.e. PTh4FBT-PERY, PTh4FBT-DTBT. The obtained polymers were characterized by UV, CV, DSC, TGA, X-ray diffraction and their performance in OTFTs and OSCs. Both PTh4FBT-PERY and PTh4FBT-DTBT show the mobilities of 4.04 × 10-1 cm2 V-1 s-1 and 1.08 × 10-1 cm2 V-1 s-1 respectively. The mobility of PTh4FBT-PERY is higher than that (2.89 × 10-1 cm2 V-1 s-1) of PTh4FBT. The PCE values of PTh4FBT-PERY and PTh4FBT-DTBT based OPV devices are 5.0% and 4.97% respectively. For the second series, silolo[3,2-b:4,5-b']bis(selenophene)(DSS) were used as an electron donor unit and it was copolymerized with dithienodiketopyrrolopyrrole (DPP) containing octyl and 2-ethylhexyl side chains to obtain two alternating copolymers, i.e. PDSSDPP-C2C6 and PDSSDPP-C8. The obtained polymers were characterized by UV, CV, DSC, TGA, X-ray diffraction and their OTFTs performance. Both PDSSDPP-C2C6 and PDSSDPP-C8 show the mobilities of 2.67 × 10-2 cm2 V-1 s-1 and 2.47 × 10-2 cm2 V-1 s-1 respectively.Both values are higher than that (3.89 × 10-3 cm2 V-1 s-1) of homologue PDTSDPP-C8. Hsu, Chain-shu 許千樹 2015 學位論文 ; thesis 129 zh-TW |
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碩士 === 國立交通大學 === 應用化學系碩博士班 === 104 === In this study, two series of conjugated polymers were synthesized for the application of organic thin film transistors (OTETs) and organic solar cells (OSCs). For the first series, perylene and dithienylbenzothiadiazole (DTBT) were introduced to the side chain of poly(5,6-difluoro-benzo-2,1,3-thiadiazole co-quaterthiophene) (PTh4FBT) to obtain two types of copolymers, i.e. PTh4FBT-PERY, PTh4FBT-DTBT. The obtained polymers were characterized by UV, CV, DSC, TGA, X-ray diffraction and their performance in OTFTs and OSCs. Both PTh4FBT-PERY and PTh4FBT-DTBT show the mobilities of 4.04 × 10-1 cm2 V-1 s-1 and 1.08 × 10-1 cm2 V-1 s-1 respectively. The mobility of PTh4FBT-PERY is higher than that (2.89 × 10-1 cm2 V-1 s-1) of PTh4FBT. The PCE values of PTh4FBT-PERY and PTh4FBT-DTBT based OPV devices are 5.0% and 4.97% respectively.
For the second series, silolo[3,2-b:4,5-b']bis(selenophene)(DSS) were used as an electron donor unit and it was copolymerized with dithienodiketopyrrolopyrrole (DPP) containing octyl and 2-ethylhexyl side chains to obtain two alternating copolymers, i.e. PDSSDPP-C2C6 and PDSSDPP-C8. The obtained polymers were characterized by UV, CV, DSC, TGA, X-ray diffraction and their OTFTs performance. Both PDSSDPP-C2C6 and PDSSDPP-C8 show the mobilities of 2.67 × 10-2 cm2 V-1 s-1 and 2.47 × 10-2 cm2 V-1 s-1 respectively.Both values are higher than that (3.89 × 10-3 cm2 V-1 s-1) of homologue PDTSDPP-C8.
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author2 |
Hsu, Chain-shu |
author_facet |
Hsu, Chain-shu Yang, Cheng-Tai 楊鎮臺 |
author |
Yang, Cheng-Tai 楊鎮臺 |
spellingShingle |
Yang, Cheng-Tai 楊鎮臺 Synthesis and Characterization of Conjugated Polymers Based on Two Dimensional 5,6-Difluoro-benzo-2,1,3-thiadiazole with Thiophene Units and Silolobis(selenophene) Based Conjugated Polymers |
author_sort |
Yang, Cheng-Tai |
title |
Synthesis and Characterization of Conjugated Polymers Based on Two Dimensional 5,6-Difluoro-benzo-2,1,3-thiadiazole with Thiophene Units and Silolobis(selenophene) Based Conjugated Polymers |
title_short |
Synthesis and Characterization of Conjugated Polymers Based on Two Dimensional 5,6-Difluoro-benzo-2,1,3-thiadiazole with Thiophene Units and Silolobis(selenophene) Based Conjugated Polymers |
title_full |
Synthesis and Characterization of Conjugated Polymers Based on Two Dimensional 5,6-Difluoro-benzo-2,1,3-thiadiazole with Thiophene Units and Silolobis(selenophene) Based Conjugated Polymers |
title_fullStr |
Synthesis and Characterization of Conjugated Polymers Based on Two Dimensional 5,6-Difluoro-benzo-2,1,3-thiadiazole with Thiophene Units and Silolobis(selenophene) Based Conjugated Polymers |
title_full_unstemmed |
Synthesis and Characterization of Conjugated Polymers Based on Two Dimensional 5,6-Difluoro-benzo-2,1,3-thiadiazole with Thiophene Units and Silolobis(selenophene) Based Conjugated Polymers |
title_sort |
synthesis and characterization of conjugated polymers based on two dimensional 5,6-difluoro-benzo-2,1,3-thiadiazole with thiophene units and silolobis(selenophene) based conjugated polymers |
publishDate |
2015 |
url |
http://ndltd.ncl.edu.tw/handle/fs8kmm |
work_keys_str_mv |
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