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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...

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Autores principales: Garcias-Morales, Cesar, Romero-Borja, Daniel, Maldonado, José-Luis, Roa, Arián E., Rodríguez, Mario, García-Merinos, J. Pablo, Ariza-Castolo, Armando
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
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%.
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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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