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Concretized structural evolution supported assembly-controlled film-forming kinetics in slot-die coated organic photovoltaics
Bulk-heterojunction structured small-area organic solar cells are approaching 20% power conversion efficiency, but the blurred film-forming kinetics in the fabrication of large-area devices causes significant PCE loss and restrains the potential of commercialization. Such blurring came from insuffic...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562442/ https://www.ncbi.nlm.nih.gov/pubmed/37813858 http://dx.doi.org/10.1038/s41467-023-42018-7 |
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author | Zhang, Hao Tian, Chenyang Zhang, Ziqi Xie, Meiling Zhang, Jianqi Zhu, Lingyun Wei, Zhixiang |
author_facet | Zhang, Hao Tian, Chenyang Zhang, Ziqi Xie, Meiling Zhang, Jianqi Zhu, Lingyun Wei, Zhixiang |
author_sort | Zhang, Hao |
collection | PubMed |
description | Bulk-heterojunction structured small-area organic solar cells are approaching 20% power conversion efficiency, but the blurred film-forming kinetics in the fabrication of large-area devices causes significant PCE loss and restrains the potential of commercialization. Such blurring came from insufficient knowledge of structural evolution during the film-forming process. Here, we concretize the evolution process with structures detailed to the submolecular level by comprehensive investigations of in-situ UV-vis spectroscopy, Atomic Force Microscope, Grazing Incident Wide Angle X-ray Scattering, and molecular dynamic simulation. With such hierarchical structural knowledge, assembly-controlled film-forming kinetics is proposed to explain the whole picture. Such assembly is determined by molecule configuration and can be tuned via external conditions. Understanding this kinetics will contribute to screening large-area device fabrication conditions, and the detailed structural knowledge could inspire the future design of novel photovoltaic materials that are intrinsically excellent in large-area device fabrications. |
format | Online Article Text |
id | pubmed-10562442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105624422023-10-11 Concretized structural evolution supported assembly-controlled film-forming kinetics in slot-die coated organic photovoltaics Zhang, Hao Tian, Chenyang Zhang, Ziqi Xie, Meiling Zhang, Jianqi Zhu, Lingyun Wei, Zhixiang Nat Commun Article Bulk-heterojunction structured small-area organic solar cells are approaching 20% power conversion efficiency, but the blurred film-forming kinetics in the fabrication of large-area devices causes significant PCE loss and restrains the potential of commercialization. Such blurring came from insufficient knowledge of structural evolution during the film-forming process. Here, we concretize the evolution process with structures detailed to the submolecular level by comprehensive investigations of in-situ UV-vis spectroscopy, Atomic Force Microscope, Grazing Incident Wide Angle X-ray Scattering, and molecular dynamic simulation. With such hierarchical structural knowledge, assembly-controlled film-forming kinetics is proposed to explain the whole picture. Such assembly is determined by molecule configuration and can be tuned via external conditions. Understanding this kinetics will contribute to screening large-area device fabrication conditions, and the detailed structural knowledge could inspire the future design of novel photovoltaic materials that are intrinsically excellent in large-area device fabrications. Nature Publishing Group UK 2023-10-09 /pmc/articles/PMC10562442/ /pubmed/37813858 http://dx.doi.org/10.1038/s41467-023-42018-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhang, Hao Tian, Chenyang Zhang, Ziqi Xie, Meiling Zhang, Jianqi Zhu, Lingyun Wei, Zhixiang Concretized structural evolution supported assembly-controlled film-forming kinetics in slot-die coated organic photovoltaics |
title | Concretized structural evolution supported assembly-controlled film-forming kinetics in slot-die coated organic photovoltaics |
title_full | Concretized structural evolution supported assembly-controlled film-forming kinetics in slot-die coated organic photovoltaics |
title_fullStr | Concretized structural evolution supported assembly-controlled film-forming kinetics in slot-die coated organic photovoltaics |
title_full_unstemmed | Concretized structural evolution supported assembly-controlled film-forming kinetics in slot-die coated organic photovoltaics |
title_short | Concretized structural evolution supported assembly-controlled film-forming kinetics in slot-die coated organic photovoltaics |
title_sort | concretized structural evolution supported assembly-controlled film-forming kinetics in slot-die coated organic photovoltaics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562442/ https://www.ncbi.nlm.nih.gov/pubmed/37813858 http://dx.doi.org/10.1038/s41467-023-42018-7 |
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