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Natural Chlorophyll-Related Porphyrins and Chlorins for Dye-Sensitized Solar Cells
Natural-chlorophyll-related porphyrins, including (2H, Zn, Cu)-protoporphyrin IX (Por-1) and Zn-mesoporphyrin IX (Por-2), and chlorins, including chlorin e(6) (Chl-1), chlorin e(4) (Chl-2), and rhodin G(7) (Chl-3), have been used in dye-sensitized solar cells (DSSCs). For porphyrin sensitizers that...
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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/PMC6268924/ https://www.ncbi.nlm.nih.gov/pubmed/22504833 http://dx.doi.org/10.3390/molecules17044484 |
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author | Wang, Xiao-Feng Kitao, Osamu |
author_facet | Wang, Xiao-Feng Kitao, Osamu |
author_sort | Wang, Xiao-Feng |
collection | PubMed |
description | Natural-chlorophyll-related porphyrins, including (2H, Zn, Cu)-protoporphyrin IX (Por-1) and Zn-mesoporphyrin IX (Por-2), and chlorins, including chlorin e(6) (Chl-1), chlorin e(4) (Chl-2), and rhodin G(7) (Chl-3), have been used in dye-sensitized solar cells (DSSCs). For porphyrin sensitizers that have vinyl groups at the β-positions, zinc coordinated Por-1 gives the highest solar-energy-to-electricity conversion efficiency (η) of up to 2.9%. Replacing the vinyl groups of ZnPor-1 with ethyl groups increases the open-circuit voltage (V(oc)) from 0.61 V to 0.66 V, but decreases the short-circuit current (J(sc)) from 7.0 mA·cm(−2) to 6.1 mA·cm(−2) and the value of η to 2.8%. Density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations suggest that the higher J(sc) values of Zn-based porphyrin sensitizers result from the favorable electron injection from the LUMO at higher energy levels. In the case of the chlorin sensitizers, the number of carboxyl protons has a large effect on the photovoltaic performance. Chl-2 with two carboxyl protons gives much higher values of J(sc), V(oc), and η than does Chl-1 with three carboxyl protons. Replacing the protons of Chl-1 with sodium ions can substantially improve the photovoltaic performance of Chl-1-based solar cells. Furthermore, the sodium salt of Chl-3 with an aldehyde group at the C7 position shows poorer photovoltaic performance than does the sodium salt of Chl-1 with methyl groups at the C7 position. This is due to the low light-harvesting capability of Chl-3. |
format | Online Article Text |
id | pubmed-6268924 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62689242018-12-11 Natural Chlorophyll-Related Porphyrins and Chlorins for Dye-Sensitized Solar Cells Wang, Xiao-Feng Kitao, Osamu Molecules Article Natural-chlorophyll-related porphyrins, including (2H, Zn, Cu)-protoporphyrin IX (Por-1) and Zn-mesoporphyrin IX (Por-2), and chlorins, including chlorin e(6) (Chl-1), chlorin e(4) (Chl-2), and rhodin G(7) (Chl-3), have been used in dye-sensitized solar cells (DSSCs). For porphyrin sensitizers that have vinyl groups at the β-positions, zinc coordinated Por-1 gives the highest solar-energy-to-electricity conversion efficiency (η) of up to 2.9%. Replacing the vinyl groups of ZnPor-1 with ethyl groups increases the open-circuit voltage (V(oc)) from 0.61 V to 0.66 V, but decreases the short-circuit current (J(sc)) from 7.0 mA·cm(−2) to 6.1 mA·cm(−2) and the value of η to 2.8%. Density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations suggest that the higher J(sc) values of Zn-based porphyrin sensitizers result from the favorable electron injection from the LUMO at higher energy levels. In the case of the chlorin sensitizers, the number of carboxyl protons has a large effect on the photovoltaic performance. Chl-2 with two carboxyl protons gives much higher values of J(sc), V(oc), and η than does Chl-1 with three carboxyl protons. Replacing the protons of Chl-1 with sodium ions can substantially improve the photovoltaic performance of Chl-1-based solar cells. Furthermore, the sodium salt of Chl-3 with an aldehyde group at the C7 position shows poorer photovoltaic performance than does the sodium salt of Chl-1 with methyl groups at the C7 position. This is due to the low light-harvesting capability of Chl-3. MDPI 2012-04-13 /pmc/articles/PMC6268924/ /pubmed/22504833 http://dx.doi.org/10.3390/molecules17044484 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 | Article Wang, Xiao-Feng Kitao, Osamu Natural Chlorophyll-Related Porphyrins and Chlorins for Dye-Sensitized Solar Cells |
title | Natural Chlorophyll-Related Porphyrins and Chlorins for Dye-Sensitized Solar Cells |
title_full | Natural Chlorophyll-Related Porphyrins and Chlorins for Dye-Sensitized Solar Cells |
title_fullStr | Natural Chlorophyll-Related Porphyrins and Chlorins for Dye-Sensitized Solar Cells |
title_full_unstemmed | Natural Chlorophyll-Related Porphyrins and Chlorins for Dye-Sensitized Solar Cells |
title_short | Natural Chlorophyll-Related Porphyrins and Chlorins for Dye-Sensitized Solar Cells |
title_sort | natural chlorophyll-related porphyrins and chlorins for dye-sensitized solar cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268924/ https://www.ncbi.nlm.nih.gov/pubmed/22504833 http://dx.doi.org/10.3390/molecules17044484 |
work_keys_str_mv | AT wangxiaofeng naturalchlorophyllrelatedporphyrinsandchlorinsfordyesensitizedsolarcells AT kitaoosamu naturalchlorophyllrelatedporphyrinsandchlorinsfordyesensitizedsolarcells |