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Small Molecules Derived from Thieno[3,4-c]pyrrole-4,6-dione (TPD) and Their Use in Solution Processed Organic Solar Cells
In this work, microwave synthesis, chemical, optical and electrochemical characterization of three small organic molecules, TPA-TPD, TPA-PT-TPD and TPA-TT-TPD with donor-acceptor structure and their use in organic photovoltaic cells are reported. For the synthesis, 5-(2-ethylhexyl)-4H-thieno[3,4-c]p...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151745/ https://www.ncbi.nlm.nih.gov/pubmed/28974003 http://dx.doi.org/10.3390/molecules22101607 |
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author | Garcias-Morales, Cesar Romero-Borja, Daniel Maldonado, José-Luis Roa, Arián E. Rodríguez, Mario García-Merinos, J. Pablo Ariza-Castolo, Armando |
author_facet | Garcias-Morales, Cesar Romero-Borja, Daniel Maldonado, José-Luis Roa, Arián E. Rodríguez, Mario García-Merinos, J. Pablo Ariza-Castolo, Armando |
author_sort | Garcias-Morales, Cesar |
collection | PubMed |
description | In this work, microwave synthesis, chemical, optical and electrochemical characterization of three small organic molecules, TPA-TPD, TPA-PT-TPD and TPA-TT-TPD with donor-acceptor structure and their use in organic photovoltaic cells are reported. For the synthesis, 5-(2-ethylhexyl)-4H-thieno[3,4-c]pyrrole-4,6(5H)-dione was used as electron withdrawing fragment while the triphenylamine was used as electron donating fragment. Molecular electronic geometry and electronic distribution density were established by density functional theory (DFT) calculations and confirmed by optical and chemical characterization. These molecules were employed as electron-donors in the active layer for manufacturing bulk heterojunction organic solar cells, where [6,6]-phenyl C71 butyric acid methyl ester (PC71BM) was used as electron-acceptor. As cathode, Field′s metal (FM), an eutectic alloy (Bi/In/Sn: 32.5%, 51%, and 16.5%, respectively) with a melting point above 62 °C, was easily deposited by drop casting under vacuum-free process and at air atmosphere. Prepared devices based on TPA-TPD:PC71BM (1:4 w/w ratio) presented a large V(OC) = 0.97 V, with J(SC) = 7.9 mA/cm(2), a FF = 0.34, then, a power conversion efficiency (PCE) of 2.6%. |
format | Online Article Text |
id | pubmed-6151745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61517452018-11-13 Small Molecules Derived from Thieno[3,4-c]pyrrole-4,6-dione (TPD) and Their Use in Solution Processed Organic Solar Cells Garcias-Morales, Cesar Romero-Borja, Daniel Maldonado, José-Luis Roa, Arián E. Rodríguez, Mario García-Merinos, J. Pablo Ariza-Castolo, Armando Molecules Article In this work, microwave synthesis, chemical, optical and electrochemical characterization of three small organic molecules, TPA-TPD, TPA-PT-TPD and TPA-TT-TPD with donor-acceptor structure and their use in organic photovoltaic cells are reported. For the synthesis, 5-(2-ethylhexyl)-4H-thieno[3,4-c]pyrrole-4,6(5H)-dione was used as electron withdrawing fragment while the triphenylamine was used as electron donating fragment. Molecular electronic geometry and electronic distribution density were established by density functional theory (DFT) calculations and confirmed by optical and chemical characterization. These molecules were employed as electron-donors in the active layer for manufacturing bulk heterojunction organic solar cells, where [6,6]-phenyl C71 butyric acid methyl ester (PC71BM) was used as electron-acceptor. As cathode, Field′s metal (FM), an eutectic alloy (Bi/In/Sn: 32.5%, 51%, and 16.5%, respectively) with a melting point above 62 °C, was easily deposited by drop casting under vacuum-free process and at air atmosphere. Prepared devices based on TPA-TPD:PC71BM (1:4 w/w ratio) presented a large V(OC) = 0.97 V, with J(SC) = 7.9 mA/cm(2), a FF = 0.34, then, a power conversion efficiency (PCE) of 2.6%. MDPI 2017-09-30 /pmc/articles/PMC6151745/ /pubmed/28974003 http://dx.doi.org/10.3390/molecules22101607 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Garcias-Morales, Cesar Romero-Borja, Daniel Maldonado, José-Luis Roa, Arián E. Rodríguez, Mario García-Merinos, J. Pablo Ariza-Castolo, Armando Small Molecules Derived from Thieno[3,4-c]pyrrole-4,6-dione (TPD) and Their Use in Solution Processed Organic Solar Cells |
title | Small Molecules Derived from Thieno[3,4-c]pyrrole-4,6-dione (TPD) and Their Use in Solution Processed Organic Solar Cells |
title_full | Small Molecules Derived from Thieno[3,4-c]pyrrole-4,6-dione (TPD) and Their Use in Solution Processed Organic Solar Cells |
title_fullStr | Small Molecules Derived from Thieno[3,4-c]pyrrole-4,6-dione (TPD) and Their Use in Solution Processed Organic Solar Cells |
title_full_unstemmed | Small Molecules Derived from Thieno[3,4-c]pyrrole-4,6-dione (TPD) and Their Use in Solution Processed Organic Solar Cells |
title_short | Small Molecules Derived from Thieno[3,4-c]pyrrole-4,6-dione (TPD) and Their Use in Solution Processed Organic Solar Cells |
title_sort | small molecules derived from thieno[3,4-c]pyrrole-4,6-dione (tpd) and their use in solution processed organic solar cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151745/ https://www.ncbi.nlm.nih.gov/pubmed/28974003 http://dx.doi.org/10.3390/molecules22101607 |
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