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Efficient Sunlight Harvesting by A(4) β-Pyrrolic Substituted Zn(II) Porphyrins: A Mini-Review
Dye-Sensitized Solar Cells (DSSCs) are a highly promising alternative to conventional photovoltaic silicon-based devices, due to the potential low cost and the interesting conversion efficiencies. A key-role is played by the dye, and porphyrin sensitizers have drawn great interest because of their e...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470396/ https://www.ncbi.nlm.nih.gov/pubmed/31032244 http://dx.doi.org/10.3389/fchem.2019.00177 |
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author | Di Carlo, Gabriele Orbelli Biroli, Alessio Pizzotti, Maddalena Tessore, Francesca |
author_facet | Di Carlo, Gabriele Orbelli Biroli, Alessio Pizzotti, Maddalena Tessore, Francesca |
author_sort | Di Carlo, Gabriele |
collection | PubMed |
description | Dye-Sensitized Solar Cells (DSSCs) are a highly promising alternative to conventional photovoltaic silicon-based devices, due to the potential low cost and the interesting conversion efficiencies. A key-role is played by the dye, and porphyrin sensitizers have drawn great interest because of their excellent light harvesting properties mimicking photosynthesis. Indeed, porphyrins are characterized by strong electronic absorption bands in the visible region up to the near infrared and by long-lived π(*) singlet excited states. Moreover, the presence of four meso and eight β-pyrrolic positions allows a fine tuning of their photoelectrochemical properties through structural modification. Trans-A(2)BC push–pull Zn(II) porphyrins, characterized by a strong and directional electron excitation process along the push–pull system, have been extensively investigated. On the other hand, A(4) β-pyrrolic substituted tetraaryl Zn(II) porphyrins, which incorporate a tetraaryl porphyrinic core as a starting material, have received lower attention, even if they are synthetically more attractive and show several advantages such as a more sterically hindered architecture and enhanced solubility in most common organic solvents. The present contribution intends to review the most prominent A(4) β-substituted Zn(II) porphyrins reported in the literature so far for application in DSSCs, focusing on the strategies employed to enhance the light harvesting capability of the dye and on a comparison with meso-substituted analogs. |
format | Online Article Text |
id | pubmed-6470396 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64703962019-04-26 Efficient Sunlight Harvesting by A(4) β-Pyrrolic Substituted Zn(II) Porphyrins: A Mini-Review Di Carlo, Gabriele Orbelli Biroli, Alessio Pizzotti, Maddalena Tessore, Francesca Front Chem Chemistry Dye-Sensitized Solar Cells (DSSCs) are a highly promising alternative to conventional photovoltaic silicon-based devices, due to the potential low cost and the interesting conversion efficiencies. A key-role is played by the dye, and porphyrin sensitizers have drawn great interest because of their excellent light harvesting properties mimicking photosynthesis. Indeed, porphyrins are characterized by strong electronic absorption bands in the visible region up to the near infrared and by long-lived π(*) singlet excited states. Moreover, the presence of four meso and eight β-pyrrolic positions allows a fine tuning of their photoelectrochemical properties through structural modification. Trans-A(2)BC push–pull Zn(II) porphyrins, characterized by a strong and directional electron excitation process along the push–pull system, have been extensively investigated. On the other hand, A(4) β-pyrrolic substituted tetraaryl Zn(II) porphyrins, which incorporate a tetraaryl porphyrinic core as a starting material, have received lower attention, even if they are synthetically more attractive and show several advantages such as a more sterically hindered architecture and enhanced solubility in most common organic solvents. The present contribution intends to review the most prominent A(4) β-substituted Zn(II) porphyrins reported in the literature so far for application in DSSCs, focusing on the strategies employed to enhance the light harvesting capability of the dye and on a comparison with meso-substituted analogs. Frontiers Media S.A. 2019-04-11 /pmc/articles/PMC6470396/ /pubmed/31032244 http://dx.doi.org/10.3389/fchem.2019.00177 Text en Copyright © 2019 Di Carlo, Orbelli Biroli, Pizzotti and Tessore. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Di Carlo, Gabriele Orbelli Biroli, Alessio Pizzotti, Maddalena Tessore, Francesca Efficient Sunlight Harvesting by A(4) β-Pyrrolic Substituted Zn(II) Porphyrins: A Mini-Review |
title | Efficient Sunlight Harvesting by A(4) β-Pyrrolic Substituted Zn(II) Porphyrins: A Mini-Review |
title_full | Efficient Sunlight Harvesting by A(4) β-Pyrrolic Substituted Zn(II) Porphyrins: A Mini-Review |
title_fullStr | Efficient Sunlight Harvesting by A(4) β-Pyrrolic Substituted Zn(II) Porphyrins: A Mini-Review |
title_full_unstemmed | Efficient Sunlight Harvesting by A(4) β-Pyrrolic Substituted Zn(II) Porphyrins: A Mini-Review |
title_short | Efficient Sunlight Harvesting by A(4) β-Pyrrolic Substituted Zn(II) Porphyrins: A Mini-Review |
title_sort | efficient sunlight harvesting by a(4) β-pyrrolic substituted zn(ii) porphyrins: a mini-review |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470396/ https://www.ncbi.nlm.nih.gov/pubmed/31032244 http://dx.doi.org/10.3389/fchem.2019.00177 |
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