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Polymer semiconductors incorporating head-to-head linked 4-alkoxy-5-(3-alkylthiophen-2-yl)thiazole

Head-to-head linked bithiophenes with planar backbones hold distinctive advantages for constructing organic semiconductors, such as good solubilizing capability, enabling narrow bandgap, and effective tuning of frontier molecular orbital (FMO) levels using minimal thiophene numbers. In order to real...

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Autores principales: Zhou, Xin, Chen, Peng, Koh, Chang Woo, Chen, Sheng, Yu, Jianwei, Zhang, Xianhe, Tang, Yumin, Bianchi, Luca, Guo, Han, Woo, Han Young, Guo, Xugang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9087827/
https://www.ncbi.nlm.nih.gov/pubmed/35547934
http://dx.doi.org/10.1039/c8ra08360f
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author Zhou, Xin
Chen, Peng
Koh, Chang Woo
Chen, Sheng
Yu, Jianwei
Zhang, Xianhe
Tang, Yumin
Bianchi, Luca
Guo, Han
Woo, Han Young
Guo, Xugang
author_facet Zhou, Xin
Chen, Peng
Koh, Chang Woo
Chen, Sheng
Yu, Jianwei
Zhang, Xianhe
Tang, Yumin
Bianchi, Luca
Guo, Han
Woo, Han Young
Guo, Xugang
author_sort Zhou, Xin
collection PubMed
description Head-to-head linked bithiophenes with planar backbones hold distinctive advantages for constructing organic semiconductors, such as good solubilizing capability, enabling narrow bandgap, and effective tuning of frontier molecular orbital (FMO) levels using minimal thiophene numbers. In order to realize planar backbone, alkoxy chains are typically installed on thiophene head positions, owing to the small van der Waals radius of oxygen atom and accompanying noncovalent S⋯O interaction. However, the strong electron donating alkoxy chains on the electron-rich thiophenes lead to elevated FMO levels, which are detrimental to material stability and device performance. Thus, a new design approach is needed to counterbalance the strong electron donating property of alkoxy chains to bring down the FMOs. In this study, we designed and synthesized a new head-to-head linked building block, 4-alkoxy-5-(3-alkylthiophen-2-yl)thiazole (TRTzOR), using an electron-deficient thiazole to replace the electron-rich thiophene. Compared to previously reported 3-alkoxy-3′-alkyl-2,2′-bithiophene (TRTOR), TRTzOR is a weaker electron donor, which considerably lowers FMOs and maintains planar backbone through the noncovalent S⋯O interaction. The new TRTzOR was copolymerized with benzothiadiazoles with distinct F numbers to yield a series of polymer semiconductors. Compared to TRTOR-based analogous polymers, these TRTzOR-based polymers have broader absorption up to 950 nm with lower-lying FMOs by 0.2–0.3 eV, and blending these polymers with PC(71)BM leads to polymer solar cells (PSCs) with improved open-circuit voltage (V(oc)) by ca. 0.1 V and a much smaller energy loss (E(loss)) as low as 0.59 eV. These results demonstrate that thiazole substitution is an effective approach to tune FMO levels for realizing higher V(oc)s in PSCs and the small E(loss) renders TRTzOR a promising building block for developing high-performance organic semiconductors.
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spelling pubmed-90878272022-05-10 Polymer semiconductors incorporating head-to-head linked 4-alkoxy-5-(3-alkylthiophen-2-yl)thiazole Zhou, Xin Chen, Peng Koh, Chang Woo Chen, Sheng Yu, Jianwei Zhang, Xianhe Tang, Yumin Bianchi, Luca Guo, Han Woo, Han Young Guo, Xugang RSC Adv Chemistry Head-to-head linked bithiophenes with planar backbones hold distinctive advantages for constructing organic semiconductors, such as good solubilizing capability, enabling narrow bandgap, and effective tuning of frontier molecular orbital (FMO) levels using minimal thiophene numbers. In order to realize planar backbone, alkoxy chains are typically installed on thiophene head positions, owing to the small van der Waals radius of oxygen atom and accompanying noncovalent S⋯O interaction. However, the strong electron donating alkoxy chains on the electron-rich thiophenes lead to elevated FMO levels, which are detrimental to material stability and device performance. Thus, a new design approach is needed to counterbalance the strong electron donating property of alkoxy chains to bring down the FMOs. In this study, we designed and synthesized a new head-to-head linked building block, 4-alkoxy-5-(3-alkylthiophen-2-yl)thiazole (TRTzOR), using an electron-deficient thiazole to replace the electron-rich thiophene. Compared to previously reported 3-alkoxy-3′-alkyl-2,2′-bithiophene (TRTOR), TRTzOR is a weaker electron donor, which considerably lowers FMOs and maintains planar backbone through the noncovalent S⋯O interaction. The new TRTzOR was copolymerized with benzothiadiazoles with distinct F numbers to yield a series of polymer semiconductors. Compared to TRTOR-based analogous polymers, these TRTzOR-based polymers have broader absorption up to 950 nm with lower-lying FMOs by 0.2–0.3 eV, and blending these polymers with PC(71)BM leads to polymer solar cells (PSCs) with improved open-circuit voltage (V(oc)) by ca. 0.1 V and a much smaller energy loss (E(loss)) as low as 0.59 eV. These results demonstrate that thiazole substitution is an effective approach to tune FMO levels for realizing higher V(oc)s in PSCs and the small E(loss) renders TRTzOR a promising building block for developing high-performance organic semiconductors. The Royal Society of Chemistry 2018-10-18 /pmc/articles/PMC9087827/ /pubmed/35547934 http://dx.doi.org/10.1039/c8ra08360f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Zhou, Xin
Chen, Peng
Koh, Chang Woo
Chen, Sheng
Yu, Jianwei
Zhang, Xianhe
Tang, Yumin
Bianchi, Luca
Guo, Han
Woo, Han Young
Guo, Xugang
Polymer semiconductors incorporating head-to-head linked 4-alkoxy-5-(3-alkylthiophen-2-yl)thiazole
title Polymer semiconductors incorporating head-to-head linked 4-alkoxy-5-(3-alkylthiophen-2-yl)thiazole
title_full Polymer semiconductors incorporating head-to-head linked 4-alkoxy-5-(3-alkylthiophen-2-yl)thiazole
title_fullStr Polymer semiconductors incorporating head-to-head linked 4-alkoxy-5-(3-alkylthiophen-2-yl)thiazole
title_full_unstemmed Polymer semiconductors incorporating head-to-head linked 4-alkoxy-5-(3-alkylthiophen-2-yl)thiazole
title_short Polymer semiconductors incorporating head-to-head linked 4-alkoxy-5-(3-alkylthiophen-2-yl)thiazole
title_sort polymer semiconductors incorporating head-to-head linked 4-alkoxy-5-(3-alkylthiophen-2-yl)thiazole
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9087827/
https://www.ncbi.nlm.nih.gov/pubmed/35547934
http://dx.doi.org/10.1039/c8ra08360f
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