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Isomerization enabling near-infrared electron acceptors
An isomerization method was utilized to yield a novel near-infrared nonfullerene acceptor DTA-IC-M. By simply changing the linking fashion between the anthracene and neighboring thiophenes, a remarkable redshift (∼170 nm) of absorption was observed from DTA-IC-S to its isomer DTA-IC-M which shows a...
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/PMC9075510/ https://www.ncbi.nlm.nih.gov/pubmed/35542245 http://dx.doi.org/10.1039/c9ra07911d |
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author | Luo, Jiasi Wang, Yang Liu, Bin Wu, Ziang Zhang, Yujie Tang, Yumin Chen, Peng Liao, Qiaogan Woo, Han Young Guo, Xugang |
author_facet | Luo, Jiasi Wang, Yang Liu, Bin Wu, Ziang Zhang, Yujie Tang, Yumin Chen, Peng Liao, Qiaogan Woo, Han Young Guo, Xugang |
author_sort | Luo, Jiasi |
collection | PubMed |
description | An isomerization method was utilized to yield a novel near-infrared nonfullerene acceptor DTA-IC-M. By simply changing the linking fashion between the anthracene and neighboring thiophenes, a remarkable redshift (∼170 nm) of absorption was observed from DTA-IC-S to its isomer DTA-IC-M which shows a maximum absorption peak over 800 nm with a narrow bandgap of 1.35 eV. Due to the enhanced photo-to-current response in the near-infrared region, an improved short-circuit current of 12.96 mA cm(−2) was achieved for the DTA-IC-M based OSCs. |
format | Online Article Text |
id | pubmed-9075510 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90755102022-05-09 Isomerization enabling near-infrared electron acceptors Luo, Jiasi Wang, Yang Liu, Bin Wu, Ziang Zhang, Yujie Tang, Yumin Chen, Peng Liao, Qiaogan Woo, Han Young Guo, Xugang RSC Adv Chemistry An isomerization method was utilized to yield a novel near-infrared nonfullerene acceptor DTA-IC-M. By simply changing the linking fashion between the anthracene and neighboring thiophenes, a remarkable redshift (∼170 nm) of absorption was observed from DTA-IC-S to its isomer DTA-IC-M which shows a maximum absorption peak over 800 nm with a narrow bandgap of 1.35 eV. Due to the enhanced photo-to-current response in the near-infrared region, an improved short-circuit current of 12.96 mA cm(−2) was achieved for the DTA-IC-M based OSCs. The Royal Society of Chemistry 2019-11-14 /pmc/articles/PMC9075510/ /pubmed/35542245 http://dx.doi.org/10.1039/c9ra07911d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Luo, Jiasi Wang, Yang Liu, Bin Wu, Ziang Zhang, Yujie Tang, Yumin Chen, Peng Liao, Qiaogan Woo, Han Young Guo, Xugang Isomerization enabling near-infrared electron acceptors |
title | Isomerization enabling near-infrared electron acceptors |
title_full | Isomerization enabling near-infrared electron acceptors |
title_fullStr | Isomerization enabling near-infrared electron acceptors |
title_full_unstemmed | Isomerization enabling near-infrared electron acceptors |
title_short | Isomerization enabling near-infrared electron acceptors |
title_sort | isomerization enabling near-infrared electron acceptors |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9075510/ https://www.ncbi.nlm.nih.gov/pubmed/35542245 http://dx.doi.org/10.1039/c9ra07911d |
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