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Organic Thin Film Transistors Incorporating Solution Processable Thieno[3,2-b]thiophene Thienoacenes

Bottom-gate bottom-contact organic thin film transistors (OTFTs) were prepared with four novel star-shaped conjugated molecules containing a fused thieno[3,2-b]thiophene moiety incorporated either in the core and/or at the periphery of the molecular framework. The molecules were soluble in CS(2), al...

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Autores principales: Rice, Nicole A., Magnan, François, Melville, Owen A., Brusso, Jaclyn L., Lessard, Benoît H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793506/
https://www.ncbi.nlm.nih.gov/pubmed/29271885
http://dx.doi.org/10.3390/ma11010008
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author Rice, Nicole A.
Magnan, François
Melville, Owen A.
Brusso, Jaclyn L.
Lessard, Benoît H.
author_facet Rice, Nicole A.
Magnan, François
Melville, Owen A.
Brusso, Jaclyn L.
Lessard, Benoît H.
author_sort Rice, Nicole A.
collection PubMed
description Bottom-gate bottom-contact organic thin film transistors (OTFTs) were prepared with four novel star-shaped conjugated molecules containing a fused thieno[3,2-b]thiophene moiety incorporated either in the core and/or at the periphery of the molecular framework. The molecules were soluble in CS(2), allowing for solution-processing techniques to be employed. OTFTs with different channel geometries were characterized in both air and vacuum in order to compare environmental effects on performance. Blending the small molecules with poly(styrene), an insulating polymer, facilitated the formation of an even semiconducting film, resulting in an order of magnitude increase in device mobility. The highest field-effect mobilities were in air and on the order of 10(−3) cm(2)/Vs for three of the four molecules, with a maximum mobility of 9.2 × 10(−3) cm(2)/Vs achieved for the most conjugated small molecule. This study explores the relationship between processing conditions and OTFT devices performance for four different molecules within this new family of materials, resulting in a deeper insight into their potential as solution-processable semiconductors.
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spelling pubmed-57935062018-02-07 Organic Thin Film Transistors Incorporating Solution Processable Thieno[3,2-b]thiophene Thienoacenes Rice, Nicole A. Magnan, François Melville, Owen A. Brusso, Jaclyn L. Lessard, Benoît H. Materials (Basel) Article Bottom-gate bottom-contact organic thin film transistors (OTFTs) were prepared with four novel star-shaped conjugated molecules containing a fused thieno[3,2-b]thiophene moiety incorporated either in the core and/or at the periphery of the molecular framework. The molecules were soluble in CS(2), allowing for solution-processing techniques to be employed. OTFTs with different channel geometries were characterized in both air and vacuum in order to compare environmental effects on performance. Blending the small molecules with poly(styrene), an insulating polymer, facilitated the formation of an even semiconducting film, resulting in an order of magnitude increase in device mobility. The highest field-effect mobilities were in air and on the order of 10(−3) cm(2)/Vs for three of the four molecules, with a maximum mobility of 9.2 × 10(−3) cm(2)/Vs achieved for the most conjugated small molecule. This study explores the relationship between processing conditions and OTFT devices performance for four different molecules within this new family of materials, resulting in a deeper insight into their potential as solution-processable semiconductors. MDPI 2017-12-22 /pmc/articles/PMC5793506/ /pubmed/29271885 http://dx.doi.org/10.3390/ma11010008 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rice, Nicole A.
Magnan, François
Melville, Owen A.
Brusso, Jaclyn L.
Lessard, Benoît H.
Organic Thin Film Transistors Incorporating Solution Processable Thieno[3,2-b]thiophene Thienoacenes
title Organic Thin Film Transistors Incorporating Solution Processable Thieno[3,2-b]thiophene Thienoacenes
title_full Organic Thin Film Transistors Incorporating Solution Processable Thieno[3,2-b]thiophene Thienoacenes
title_fullStr Organic Thin Film Transistors Incorporating Solution Processable Thieno[3,2-b]thiophene Thienoacenes
title_full_unstemmed Organic Thin Film Transistors Incorporating Solution Processable Thieno[3,2-b]thiophene Thienoacenes
title_short Organic Thin Film Transistors Incorporating Solution Processable Thieno[3,2-b]thiophene Thienoacenes
title_sort organic thin film transistors incorporating solution processable thieno[3,2-b]thiophene thienoacenes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793506/
https://www.ncbi.nlm.nih.gov/pubmed/29271885
http://dx.doi.org/10.3390/ma11010008
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