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Diketopyrrolopyrrole-based acceptors with multi-arms for organic solar cells
Three small molecules SBF-1DPPDCV, SBF-2DPPDCV and SBF-4DPPDCV consisting of a spirobifluorene (SBF) unit as the core and one, two, and four diketopyrrolopyrrole dicyanovinyl (DPPDCV) units as the arms have been designed and synthesized for solution-processed bulk-heterojunction (BHJ) solar cells. T...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082300/ https://www.ncbi.nlm.nih.gov/pubmed/35542151 http://dx.doi.org/10.1039/c8ra03792b |
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author | Sun, Po Li, Xiangzhi Wang, Yulong Shan, Haiquan Xu, Jiaju Liu, Changmei Zhang, Cong Chen, Fei Xu, Zongxiang Chen, Zhi-kuan Huang, Wei |
author_facet | Sun, Po Li, Xiangzhi Wang, Yulong Shan, Haiquan Xu, Jiaju Liu, Changmei Zhang, Cong Chen, Fei Xu, Zongxiang Chen, Zhi-kuan Huang, Wei |
author_sort | Sun, Po |
collection | PubMed |
description | Three small molecules SBF-1DPPDCV, SBF-2DPPDCV and SBF-4DPPDCV consisting of a spirobifluorene (SBF) unit as the core and one, two, and four diketopyrrolopyrrole dicyanovinyl (DPPDCV) units as the arms have been designed and synthesized for solution-processed bulk-heterojunction (BHJ) solar cells. The UV-Vis absorption and cyclic voltammetry measurement of these compounds showed that all these compounds have an intense absorption band over 300–750 nm with a LUMO energy level at around −3.87 eV. When pairing with PTB7-Th as the donor, devices fabricated based on PTB7-Th : SBF-4DPPDCV blends showed a decent PCE of 3.85%, which is the highest power conversion efficiency (PCE) amongst the three DPP acceptor fabricated devices without extra treatment. Devices with SBF-1DPPDCV and SBF-2DPPDCV acceptors showed lower PCEs of 0.26% for SBF-1DPPDCV and 0.98% for SBF-2DPPDCV respectively. The three dimensional (3D) structure of SBF-4DPPDCV facilitates the formation of a 3D charge-transport network and thus enables a rational electron-transport ability (1.04 × 10(−4) cm(2) V(−1) s(−1)), which further leads to a higher J(sc) (10.71 mA cm(−2)). These findings suggest that multi-arm acceptors present better performance than one-arm or two-arm molecules for organic solar cells. |
format | Online Article Text |
id | pubmed-9082300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90823002022-05-09 Diketopyrrolopyrrole-based acceptors with multi-arms for organic solar cells Sun, Po Li, Xiangzhi Wang, Yulong Shan, Haiquan Xu, Jiaju Liu, Changmei Zhang, Cong Chen, Fei Xu, Zongxiang Chen, Zhi-kuan Huang, Wei RSC Adv Chemistry Three small molecules SBF-1DPPDCV, SBF-2DPPDCV and SBF-4DPPDCV consisting of a spirobifluorene (SBF) unit as the core and one, two, and four diketopyrrolopyrrole dicyanovinyl (DPPDCV) units as the arms have been designed and synthesized for solution-processed bulk-heterojunction (BHJ) solar cells. The UV-Vis absorption and cyclic voltammetry measurement of these compounds showed that all these compounds have an intense absorption band over 300–750 nm with a LUMO energy level at around −3.87 eV. When pairing with PTB7-Th as the donor, devices fabricated based on PTB7-Th : SBF-4DPPDCV blends showed a decent PCE of 3.85%, which is the highest power conversion efficiency (PCE) amongst the three DPP acceptor fabricated devices without extra treatment. Devices with SBF-1DPPDCV and SBF-2DPPDCV acceptors showed lower PCEs of 0.26% for SBF-1DPPDCV and 0.98% for SBF-2DPPDCV respectively. The three dimensional (3D) structure of SBF-4DPPDCV facilitates the formation of a 3D charge-transport network and thus enables a rational electron-transport ability (1.04 × 10(−4) cm(2) V(−1) s(−1)), which further leads to a higher J(sc) (10.71 mA cm(−2)). These findings suggest that multi-arm acceptors present better performance than one-arm or two-arm molecules for organic solar cells. The Royal Society of Chemistry 2018-07-12 /pmc/articles/PMC9082300/ /pubmed/35542151 http://dx.doi.org/10.1039/c8ra03792b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Sun, Po Li, Xiangzhi Wang, Yulong Shan, Haiquan Xu, Jiaju Liu, Changmei Zhang, Cong Chen, Fei Xu, Zongxiang Chen, Zhi-kuan Huang, Wei Diketopyrrolopyrrole-based acceptors with multi-arms for organic solar cells |
title | Diketopyrrolopyrrole-based acceptors with multi-arms for organic solar cells |
title_full | Diketopyrrolopyrrole-based acceptors with multi-arms for organic solar cells |
title_fullStr | Diketopyrrolopyrrole-based acceptors with multi-arms for organic solar cells |
title_full_unstemmed | Diketopyrrolopyrrole-based acceptors with multi-arms for organic solar cells |
title_short | Diketopyrrolopyrrole-based acceptors with multi-arms for organic solar cells |
title_sort | diketopyrrolopyrrole-based acceptors with multi-arms for organic solar cells |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082300/ https://www.ncbi.nlm.nih.gov/pubmed/35542151 http://dx.doi.org/10.1039/c8ra03792b |
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