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Cathode engineering with perylene-diimide interlayer enabling over 17% efficiency single-junction organic solar cells
In organic solar cells (OSCs), cathode interfacial materials are generally designed with highly polar groups to increase the capability of lowering the work function of cathode. However, the strong polar group could result in a high surface energy and poor physical contact at the active layer surfac...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264349/ https://www.ncbi.nlm.nih.gov/pubmed/32483159 http://dx.doi.org/10.1038/s41467-020-16509-w |
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author | Yao, Jia Qiu, Beibei Zhang, Zhi-Guo Xue, Lingwei Wang, Rui Zhang, Chunfeng Chen, Shanshan Zhou, Qiuju Sun, Chenkai Yang, Changduk Xiao, Min Meng, Lei Li, Yongfang |
author_facet | Yao, Jia Qiu, Beibei Zhang, Zhi-Guo Xue, Lingwei Wang, Rui Zhang, Chunfeng Chen, Shanshan Zhou, Qiuju Sun, Chenkai Yang, Changduk Xiao, Min Meng, Lei Li, Yongfang |
author_sort | Yao, Jia |
collection | PubMed |
description | In organic solar cells (OSCs), cathode interfacial materials are generally designed with highly polar groups to increase the capability of lowering the work function of cathode. However, the strong polar group could result in a high surface energy and poor physical contact at the active layer surface, posing a challenge for interlayer engineering to address the trade-off between device stability and efficiency. Herein, we report a hydrogen-bonding interfacial material, aliphatic amine-functionalized perylene-diimide (PDINN), which simultaneously down-shifts the work function of the air stable cathodes (silver and copper), and maintains good interfacial contact with the active layer. The OSCs based on PDINN engineered silver-cathode demonstrate a high power conversion efficiency of 17.23% (certified value 16.77% by NREL) and high stability. Our results indicate that PDINN is an effective cathode interfacial material and interlayer engineering via suitable intermolecular interactions is a feasible approach to improve device performance of OSCs. |
format | Online Article Text |
id | pubmed-7264349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72643492020-06-12 Cathode engineering with perylene-diimide interlayer enabling over 17% efficiency single-junction organic solar cells Yao, Jia Qiu, Beibei Zhang, Zhi-Guo Xue, Lingwei Wang, Rui Zhang, Chunfeng Chen, Shanshan Zhou, Qiuju Sun, Chenkai Yang, Changduk Xiao, Min Meng, Lei Li, Yongfang Nat Commun Article In organic solar cells (OSCs), cathode interfacial materials are generally designed with highly polar groups to increase the capability of lowering the work function of cathode. However, the strong polar group could result in a high surface energy and poor physical contact at the active layer surface, posing a challenge for interlayer engineering to address the trade-off between device stability and efficiency. Herein, we report a hydrogen-bonding interfacial material, aliphatic amine-functionalized perylene-diimide (PDINN), which simultaneously down-shifts the work function of the air stable cathodes (silver and copper), and maintains good interfacial contact with the active layer. The OSCs based on PDINN engineered silver-cathode demonstrate a high power conversion efficiency of 17.23% (certified value 16.77% by NREL) and high stability. Our results indicate that PDINN is an effective cathode interfacial material and interlayer engineering via suitable intermolecular interactions is a feasible approach to improve device performance of OSCs. Nature Publishing Group UK 2020-06-01 /pmc/articles/PMC7264349/ /pubmed/32483159 http://dx.doi.org/10.1038/s41467-020-16509-w Text en © The Author(s) 2020 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/. |
spellingShingle | Article Yao, Jia Qiu, Beibei Zhang, Zhi-Guo Xue, Lingwei Wang, Rui Zhang, Chunfeng Chen, Shanshan Zhou, Qiuju Sun, Chenkai Yang, Changduk Xiao, Min Meng, Lei Li, Yongfang Cathode engineering with perylene-diimide interlayer enabling over 17% efficiency single-junction organic solar cells |
title | Cathode engineering with perylene-diimide interlayer enabling over 17% efficiency single-junction organic solar cells |
title_full | Cathode engineering with perylene-diimide interlayer enabling over 17% efficiency single-junction organic solar cells |
title_fullStr | Cathode engineering with perylene-diimide interlayer enabling over 17% efficiency single-junction organic solar cells |
title_full_unstemmed | Cathode engineering with perylene-diimide interlayer enabling over 17% efficiency single-junction organic solar cells |
title_short | Cathode engineering with perylene-diimide interlayer enabling over 17% efficiency single-junction organic solar cells |
title_sort | cathode engineering with perylene-diimide interlayer enabling over 17% efficiency single-junction organic solar cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264349/ https://www.ncbi.nlm.nih.gov/pubmed/32483159 http://dx.doi.org/10.1038/s41467-020-16509-w |
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