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13.4 % Efficiency from All‐Small‐Molecule Organic Solar Cells Based on a Crystalline Donor with Chlorine and Trialkylsilyl Substitutions

How to simultaneously achieve both high open‐circuit voltage (V (oc)) and high short‐circuit current density (J (sc)) is a big challenge for realising high power conversion efficiency (PCE) in all‐small‐molecule organic solar cells (all‐SM OSCs). Herein, a novel small molecule (SM)‐donor, namely FYS...

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Autores principales: Su, Wenyan, Wang, Yang, Yin, Zhihong, Fan, Qunping, Guo, Xia, Yu, Liyang, Li, Yuxiang, Hou, Lintao, Zhang, Maojie, Peng, Qiang, Li, Yongfang, Wang, Ergang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518815/
https://www.ncbi.nlm.nih.gov/pubmed/34057293
http://dx.doi.org/10.1002/cssc.202100860
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author Su, Wenyan
Wang, Yang
Yin, Zhihong
Fan, Qunping
Guo, Xia
Yu, Liyang
Li, Yuxiang
Hou, Lintao
Zhang, Maojie
Peng, Qiang
Li, Yongfang
Wang, Ergang
author_facet Su, Wenyan
Wang, Yang
Yin, Zhihong
Fan, Qunping
Guo, Xia
Yu, Liyang
Li, Yuxiang
Hou, Lintao
Zhang, Maojie
Peng, Qiang
Li, Yongfang
Wang, Ergang
author_sort Su, Wenyan
collection PubMed
description How to simultaneously achieve both high open‐circuit voltage (V (oc)) and high short‐circuit current density (J (sc)) is a big challenge for realising high power conversion efficiency (PCE) in all‐small‐molecule organic solar cells (all‐SM OSCs). Herein, a novel small molecule (SM)‐donor, namely FYSM−SiCl, with trialkylsilyl and chlorine substitutions was designed and synthesized. Compared to the original SM‐donor FYSM−H, FYSM−Si with trialkylsilyl substitution showed a decreased crystallinity and lower highest occupied molecular orbital (HOMO) level, while FYSM−SiCl had an improved crystallinity, more ordered packing arrangement, significantly lower HOMO level, and predominant “face‐on” orientation. Matched with a SM‐acceptor Y6, the FYSM−SiCl‐based all‐SM OSCs exhibited both high V (oc) of 0.85 V and high J (sc) of 23.7 mA cm(−2), which is rare for all‐SM OSCs and could be attributed to the low HOMO level of FYSM−SiCl donor and the delicate balance between high crystallinity and suitable blend morphology. As a result, FYSM−SiCl achieved a high PCE of 13.4 % in all‐SM OSCs, which was much higher than those of the FYSM−H‐ (10.9 %) and FYSM−Si‐based devices (12.2 %). This work demonstrated a promising method for the design of efficient SM‐donors by a side‐chain engineering strategy via the introduction of trialkylsilyl and chlorine substitutions.
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spelling pubmed-85188152021-10-21 13.4 % Efficiency from All‐Small‐Molecule Organic Solar Cells Based on a Crystalline Donor with Chlorine and Trialkylsilyl Substitutions Su, Wenyan Wang, Yang Yin, Zhihong Fan, Qunping Guo, Xia Yu, Liyang Li, Yuxiang Hou, Lintao Zhang, Maojie Peng, Qiang Li, Yongfang Wang, Ergang ChemSusChem Full Papers How to simultaneously achieve both high open‐circuit voltage (V (oc)) and high short‐circuit current density (J (sc)) is a big challenge for realising high power conversion efficiency (PCE) in all‐small‐molecule organic solar cells (all‐SM OSCs). Herein, a novel small molecule (SM)‐donor, namely FYSM−SiCl, with trialkylsilyl and chlorine substitutions was designed and synthesized. Compared to the original SM‐donor FYSM−H, FYSM−Si with trialkylsilyl substitution showed a decreased crystallinity and lower highest occupied molecular orbital (HOMO) level, while FYSM−SiCl had an improved crystallinity, more ordered packing arrangement, significantly lower HOMO level, and predominant “face‐on” orientation. Matched with a SM‐acceptor Y6, the FYSM−SiCl‐based all‐SM OSCs exhibited both high V (oc) of 0.85 V and high J (sc) of 23.7 mA cm(−2), which is rare for all‐SM OSCs and could be attributed to the low HOMO level of FYSM−SiCl donor and the delicate balance between high crystallinity and suitable blend morphology. As a result, FYSM−SiCl achieved a high PCE of 13.4 % in all‐SM OSCs, which was much higher than those of the FYSM−H‐ (10.9 %) and FYSM−Si‐based devices (12.2 %). This work demonstrated a promising method for the design of efficient SM‐donors by a side‐chain engineering strategy via the introduction of trialkylsilyl and chlorine substitutions. John Wiley and Sons Inc. 2021-06-19 2021-09-06 /pmc/articles/PMC8518815/ /pubmed/34057293 http://dx.doi.org/10.1002/cssc.202100860 Text en © 2021 The Authors. ChemSusChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Full Papers
Su, Wenyan
Wang, Yang
Yin, Zhihong
Fan, Qunping
Guo, Xia
Yu, Liyang
Li, Yuxiang
Hou, Lintao
Zhang, Maojie
Peng, Qiang
Li, Yongfang
Wang, Ergang
13.4 % Efficiency from All‐Small‐Molecule Organic Solar Cells Based on a Crystalline Donor with Chlorine and Trialkylsilyl Substitutions
title 13.4 % Efficiency from All‐Small‐Molecule Organic Solar Cells Based on a Crystalline Donor with Chlorine and Trialkylsilyl Substitutions
title_full 13.4 % Efficiency from All‐Small‐Molecule Organic Solar Cells Based on a Crystalline Donor with Chlorine and Trialkylsilyl Substitutions
title_fullStr 13.4 % Efficiency from All‐Small‐Molecule Organic Solar Cells Based on a Crystalline Donor with Chlorine and Trialkylsilyl Substitutions
title_full_unstemmed 13.4 % Efficiency from All‐Small‐Molecule Organic Solar Cells Based on a Crystalline Donor with Chlorine and Trialkylsilyl Substitutions
title_short 13.4 % Efficiency from All‐Small‐Molecule Organic Solar Cells Based on a Crystalline Donor with Chlorine and Trialkylsilyl Substitutions
title_sort 13.4 % efficiency from all‐small‐molecule organic solar cells based on a crystalline donor with chlorine and trialkylsilyl substitutions
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518815/
https://www.ncbi.nlm.nih.gov/pubmed/34057293
http://dx.doi.org/10.1002/cssc.202100860
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