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[2,2′-Bithiophene]-4,4′-dicarboxamide: a novel building block for semiconducting polymers
A novel electron deficient building block [2,2′-bithiophene]-4,4′-dicarboxamide (BTDCA) was designed to lower the highest occupied molecular orbital (HOMO) energy level of polythiophenes in order to achieve a higher open circuit voltage (V(oc)) and thus a higher power conversion efficiency in polyme...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072092/ https://www.ncbi.nlm.nih.gov/pubmed/35530252 http://dx.doi.org/10.1039/c9ra06909g |
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author | Zhou, Xiaocheng Zhang, Zhifang Hendsbee, Arthur D. Ngai, Jenner H. L. Kumar, Pankaj Ye, Shuyang Seferos, Dwight S. Li, Yuning |
author_facet | Zhou, Xiaocheng Zhang, Zhifang Hendsbee, Arthur D. Ngai, Jenner H. L. Kumar, Pankaj Ye, Shuyang Seferos, Dwight S. Li, Yuning |
author_sort | Zhou, Xiaocheng |
collection | PubMed |
description | A novel electron deficient building block [2,2′-bithiophene]-4,4′-dicarboxamide (BTDCA) was designed to lower the highest occupied molecular orbital (HOMO) energy level of polythiophenes in order to achieve a higher open circuit voltage (V(oc)) and thus a higher power conversion efficiency in polymer solar cells (PSCs). BTDCA dibromo monomers were conveniently synthesized in four steps, and were used to prepare three thiophene-based D-A polymers, P(BTDCA66-BT) (66BT), P(BTDCA44-BT) (44BT) and P(BTDCA44-TT) (44TT). All the polymers exhibited unipolar hole transport properties, exhibiting mobilities in the range of ∼10(−4) to 10(−2) cm(2) V(−1) s(−1) with the highest hole mobility of up to 1.43 × 10(−2) cm(2) V(−1) s(−1) achieved for 44BT in bottom-gate bottom-contact organic thin film transistors (OTFTs). In PSCs, these polymers achieved high V(oc)'s of 0.81–0.87 V when PCBM or ITIC was used as acceptor. When 44TT was used as donor and ITIC was used as acceptor, a power conversion efficiency (PCE) of up to 4.5% was obtained, a significant improvement when compared with the poly(3-hexylthiophene) (P3HT):ITIC devices, which showed the highest PCE of merely 0.92%. |
format | Online Article Text |
id | pubmed-9072092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90720922022-05-06 [2,2′-Bithiophene]-4,4′-dicarboxamide: a novel building block for semiconducting polymers Zhou, Xiaocheng Zhang, Zhifang Hendsbee, Arthur D. Ngai, Jenner H. L. Kumar, Pankaj Ye, Shuyang Seferos, Dwight S. Li, Yuning RSC Adv Chemistry A novel electron deficient building block [2,2′-bithiophene]-4,4′-dicarboxamide (BTDCA) was designed to lower the highest occupied molecular orbital (HOMO) energy level of polythiophenes in order to achieve a higher open circuit voltage (V(oc)) and thus a higher power conversion efficiency in polymer solar cells (PSCs). BTDCA dibromo monomers were conveniently synthesized in four steps, and were used to prepare three thiophene-based D-A polymers, P(BTDCA66-BT) (66BT), P(BTDCA44-BT) (44BT) and P(BTDCA44-TT) (44TT). All the polymers exhibited unipolar hole transport properties, exhibiting mobilities in the range of ∼10(−4) to 10(−2) cm(2) V(−1) s(−1) with the highest hole mobility of up to 1.43 × 10(−2) cm(2) V(−1) s(−1) achieved for 44BT in bottom-gate bottom-contact organic thin film transistors (OTFTs). In PSCs, these polymers achieved high V(oc)'s of 0.81–0.87 V when PCBM or ITIC was used as acceptor. When 44TT was used as donor and ITIC was used as acceptor, a power conversion efficiency (PCE) of up to 4.5% was obtained, a significant improvement when compared with the poly(3-hexylthiophene) (P3HT):ITIC devices, which showed the highest PCE of merely 0.92%. The Royal Society of Chemistry 2019-09-25 /pmc/articles/PMC9072092/ /pubmed/35530252 http://dx.doi.org/10.1039/c9ra06909g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Zhou, Xiaocheng Zhang, Zhifang Hendsbee, Arthur D. Ngai, Jenner H. L. Kumar, Pankaj Ye, Shuyang Seferos, Dwight S. Li, Yuning [2,2′-Bithiophene]-4,4′-dicarboxamide: a novel building block for semiconducting polymers |
title | [2,2′-Bithiophene]-4,4′-dicarboxamide: a novel building block for semiconducting polymers |
title_full | [2,2′-Bithiophene]-4,4′-dicarboxamide: a novel building block for semiconducting polymers |
title_fullStr | [2,2′-Bithiophene]-4,4′-dicarboxamide: a novel building block for semiconducting polymers |
title_full_unstemmed | [2,2′-Bithiophene]-4,4′-dicarboxamide: a novel building block for semiconducting polymers |
title_short | [2,2′-Bithiophene]-4,4′-dicarboxamide: a novel building block for semiconducting polymers |
title_sort | [2,2′-bithiophene]-4,4′-dicarboxamide: a novel building block for semiconducting polymers |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072092/ https://www.ncbi.nlm.nih.gov/pubmed/35530252 http://dx.doi.org/10.1039/c9ra06909g |
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