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New Oxindole-Bridged Acceptors for Organic Sensitizers: Substitution and Performance Studies in Dye-Sensitized Solar Cells
New D-π-A configured organic sensitizers featuring halogen-substituted oxindole-bridged acceptor units have been synthesized for dye-sensitized solar cells applications. Among fluorine, bromine, and iodine substitution, the cell based on bromine incorporated dye exhibited the highest efficiency. The...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248932/ https://www.ncbi.nlm.nih.gov/pubmed/32380749 http://dx.doi.org/10.3390/molecules25092159 |
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author | Tingare, Yogesh S. Su, Chaochin Shen, Ming-Tai Tsai, Sheng-Han Ho, Shih-Yu Li, Wen-Ren |
author_facet | Tingare, Yogesh S. Su, Chaochin Shen, Ming-Tai Tsai, Sheng-Han Ho, Shih-Yu Li, Wen-Ren |
author_sort | Tingare, Yogesh S. |
collection | PubMed |
description | New D-π-A configured organic sensitizers featuring halogen-substituted oxindole-bridged acceptor units have been synthesized for dye-sensitized solar cells applications. Among fluorine, bromine, and iodine substitution, the cell based on bromine incorporated dye exhibited the highest efficiency. The oxindoles in these sensitizers were found to assist the electron injection through the chelation of their amide carbonyl groups to the TiO(2) surface. This study provides an alternate approach for future rational dye design to gain excellent DSSC performance. |
format | Online Article Text |
id | pubmed-7248932 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72489322020-06-10 New Oxindole-Bridged Acceptors for Organic Sensitizers: Substitution and Performance Studies in Dye-Sensitized Solar Cells Tingare, Yogesh S. Su, Chaochin Shen, Ming-Tai Tsai, Sheng-Han Ho, Shih-Yu Li, Wen-Ren Molecules Article New D-π-A configured organic sensitizers featuring halogen-substituted oxindole-bridged acceptor units have been synthesized for dye-sensitized solar cells applications. Among fluorine, bromine, and iodine substitution, the cell based on bromine incorporated dye exhibited the highest efficiency. The oxindoles in these sensitizers were found to assist the electron injection through the chelation of their amide carbonyl groups to the TiO(2) surface. This study provides an alternate approach for future rational dye design to gain excellent DSSC performance. MDPI 2020-05-05 /pmc/articles/PMC7248932/ /pubmed/32380749 http://dx.doi.org/10.3390/molecules25092159 Text en © 2020 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 Tingare, Yogesh S. Su, Chaochin Shen, Ming-Tai Tsai, Sheng-Han Ho, Shih-Yu Li, Wen-Ren New Oxindole-Bridged Acceptors for Organic Sensitizers: Substitution and Performance Studies in Dye-Sensitized Solar Cells |
title | New Oxindole-Bridged Acceptors for Organic Sensitizers: Substitution and Performance Studies in Dye-Sensitized Solar Cells |
title_full | New Oxindole-Bridged Acceptors for Organic Sensitizers: Substitution and Performance Studies in Dye-Sensitized Solar Cells |
title_fullStr | New Oxindole-Bridged Acceptors for Organic Sensitizers: Substitution and Performance Studies in Dye-Sensitized Solar Cells |
title_full_unstemmed | New Oxindole-Bridged Acceptors for Organic Sensitizers: Substitution and Performance Studies in Dye-Sensitized Solar Cells |
title_short | New Oxindole-Bridged Acceptors for Organic Sensitizers: Substitution and Performance Studies in Dye-Sensitized Solar Cells |
title_sort | new oxindole-bridged acceptors for organic sensitizers: substitution and performance studies in dye-sensitized solar cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248932/ https://www.ncbi.nlm.nih.gov/pubmed/32380749 http://dx.doi.org/10.3390/molecules25092159 |
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