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Mechanisms of Suppression and Enhancement of Photocurrent/Conversion Efficiency in Dye-Sensitized Solar-Cells Using Carotenoid and Chlorophyll Derivatives as Sensitizers
The mechanisms of suppression and enhancement of photocurrent/conversion efficiency (performance) in dye-sensitized solar cells, using carotenoid and chlorophyll derivatives as sensitizers, were compared systematically. The key factor to enhance the performance was found to be how to minimize intera...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268579/ https://www.ncbi.nlm.nih.gov/pubmed/22357317 http://dx.doi.org/10.3390/molecules17022188 |
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author | Koyama, Yasushi Kakitani, Yoshinori Nagae, Hiroyoshi |
author_facet | Koyama, Yasushi Kakitani, Yoshinori Nagae, Hiroyoshi |
author_sort | Koyama, Yasushi |
collection | PubMed |
description | The mechanisms of suppression and enhancement of photocurrent/conversion efficiency (performance) in dye-sensitized solar cells, using carotenoid and chlorophyll derivatives as sensitizers, were compared systematically. The key factor to enhance the performance was found to be how to minimize interaction among the excited-state dye-sensitizer(s). In a set of retinoic-acid (RA) and carotenoic-acid (CA) sensitizers, having n conjugated double bonds, CA7 gave rise to the highest performance, which was reduced toward RA5 and CA13. The former was ascribed to the generation of triplet and the resultant singlet-triplet annihilation reaction, while the latter, to the intrinsic electron injection efficiency. In a set of shorter polyene sensitizers having different polarizabilities, the one with the highest polarizability (the highest trend of aggregate formation) exhibited the higher performance toward the lower dye concentration and the lower light intensity, contrary to our expectation. This is ascribed to a decrease in the singlet-triplet annihilation reaction. The performance of cosensitization, by a pair of pheophorbide sensitizers without and with the central metal, Mg or Zn, was enhanced by the light absorption (complementary rather than competitive), the transition-dipole moments (orthogonal rather than parallel) and by the pathways of electron injection (energetically independent rather than interactive). |
format | Online Article Text |
id | pubmed-6268579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62685792018-12-10 Mechanisms of Suppression and Enhancement of Photocurrent/Conversion Efficiency in Dye-Sensitized Solar-Cells Using Carotenoid and Chlorophyll Derivatives as Sensitizers Koyama, Yasushi Kakitani, Yoshinori Nagae, Hiroyoshi Molecules Review The mechanisms of suppression and enhancement of photocurrent/conversion efficiency (performance) in dye-sensitized solar cells, using carotenoid and chlorophyll derivatives as sensitizers, were compared systematically. The key factor to enhance the performance was found to be how to minimize interaction among the excited-state dye-sensitizer(s). In a set of retinoic-acid (RA) and carotenoic-acid (CA) sensitizers, having n conjugated double bonds, CA7 gave rise to the highest performance, which was reduced toward RA5 and CA13. The former was ascribed to the generation of triplet and the resultant singlet-triplet annihilation reaction, while the latter, to the intrinsic electron injection efficiency. In a set of shorter polyene sensitizers having different polarizabilities, the one with the highest polarizability (the highest trend of aggregate formation) exhibited the higher performance toward the lower dye concentration and the lower light intensity, contrary to our expectation. This is ascribed to a decrease in the singlet-triplet annihilation reaction. The performance of cosensitization, by a pair of pheophorbide sensitizers without and with the central metal, Mg or Zn, was enhanced by the light absorption (complementary rather than competitive), the transition-dipole moments (orthogonal rather than parallel) and by the pathways of electron injection (energetically independent rather than interactive). MDPI 2012-02-22 /pmc/articles/PMC6268579/ /pubmed/22357317 http://dx.doi.org/10.3390/molecules17022188 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Koyama, Yasushi Kakitani, Yoshinori Nagae, Hiroyoshi Mechanisms of Suppression and Enhancement of Photocurrent/Conversion Efficiency in Dye-Sensitized Solar-Cells Using Carotenoid and Chlorophyll Derivatives as Sensitizers |
title | Mechanisms of Suppression and Enhancement of Photocurrent/Conversion Efficiency in Dye-Sensitized Solar-Cells Using Carotenoid and Chlorophyll Derivatives as Sensitizers |
title_full | Mechanisms of Suppression and Enhancement of Photocurrent/Conversion Efficiency in Dye-Sensitized Solar-Cells Using Carotenoid and Chlorophyll Derivatives as Sensitizers |
title_fullStr | Mechanisms of Suppression and Enhancement of Photocurrent/Conversion Efficiency in Dye-Sensitized Solar-Cells Using Carotenoid and Chlorophyll Derivatives as Sensitizers |
title_full_unstemmed | Mechanisms of Suppression and Enhancement of Photocurrent/Conversion Efficiency in Dye-Sensitized Solar-Cells Using Carotenoid and Chlorophyll Derivatives as Sensitizers |
title_short | Mechanisms of Suppression and Enhancement of Photocurrent/Conversion Efficiency in Dye-Sensitized Solar-Cells Using Carotenoid and Chlorophyll Derivatives as Sensitizers |
title_sort | mechanisms of suppression and enhancement of photocurrent/conversion efficiency in dye-sensitized solar-cells using carotenoid and chlorophyll derivatives as sensitizers |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268579/ https://www.ncbi.nlm.nih.gov/pubmed/22357317 http://dx.doi.org/10.3390/molecules17022188 |
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