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The molecular engineering, synthesis and photovoltaic studies of a novel highly efficient Ru(ii) complex incorporating a bulky TPA ancillary ligand for DSSCs: donor versus π-spacer effects
A novel Ru(ii) complex, denoted as IA-7, incorporating a bulky donor antenna, was synthesized and characterized as a promising inexpensive alternative to conventional p–n junction solar cells to study the influence of a bulky donor antenna on the light harvesting efficiency (LHE), ground and excited...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9047394/ https://www.ncbi.nlm.nih.gov/pubmed/35492570 http://dx.doi.org/10.1039/c9ra06150a |
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author | Abdellah, Islam M. El-Shafei, Ahmed |
author_facet | Abdellah, Islam M. El-Shafei, Ahmed |
author_sort | Abdellah, Islam M. |
collection | PubMed |
description | A novel Ru(ii) complex, denoted as IA-7, incorporating a bulky donor antenna, was synthesized and characterized as a promising inexpensive alternative to conventional p–n junction solar cells to study the influence of a bulky donor antenna on the light harvesting efficiency (LHE), ground and excited state oxidation potentials and total conversion efficiency of sunlight to electricity (% η) for dye-sensitized solar cells (DSSCs), and the device performance was compared to devices with MH-12 and MH-13 dyes. The incorporation of the bulky donor enriched triphenylamine (TPA) antenna resulted in a considerable increase in J(SC) and η values for DSSCs, where IA-7 outperformed MH-12 and MH-13 in terms of the total conversion efficiency and achieved a power conversion efficiency (η) of 8.86% under full sunlight irradiation (100 mW cm(−2)), compared to 8.09% for MH-12 and 8.53% for MH-13, which can be ascribed to the high open circuit voltage (V(OC)) of IA-7. Molecular engineering utilizing DFT/TD-DFT was employed to calculate the electronic properties of IA-7, including the HOMO/LUMO isosurfaces, the lowest singlet–singlet electronic transitions (E(0–0)), and the ground and excited state oxidation potentials, which were in ideal agreement with the empirical results. The electronic distribution of IA-7 indicated that the HOMO is delocalized not only on Ru and NCS, but also on the substituted TPA, and the LUMO is delocalized over 4,4′-bipyridyl dicarboxylic acid. |
format | Online Article Text |
id | pubmed-9047394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90473942022-04-28 The molecular engineering, synthesis and photovoltaic studies of a novel highly efficient Ru(ii) complex incorporating a bulky TPA ancillary ligand for DSSCs: donor versus π-spacer effects Abdellah, Islam M. El-Shafei, Ahmed RSC Adv Chemistry A novel Ru(ii) complex, denoted as IA-7, incorporating a bulky donor antenna, was synthesized and characterized as a promising inexpensive alternative to conventional p–n junction solar cells to study the influence of a bulky donor antenna on the light harvesting efficiency (LHE), ground and excited state oxidation potentials and total conversion efficiency of sunlight to electricity (% η) for dye-sensitized solar cells (DSSCs), and the device performance was compared to devices with MH-12 and MH-13 dyes. The incorporation of the bulky donor enriched triphenylamine (TPA) antenna resulted in a considerable increase in J(SC) and η values for DSSCs, where IA-7 outperformed MH-12 and MH-13 in terms of the total conversion efficiency and achieved a power conversion efficiency (η) of 8.86% under full sunlight irradiation (100 mW cm(−2)), compared to 8.09% for MH-12 and 8.53% for MH-13, which can be ascribed to the high open circuit voltage (V(OC)) of IA-7. Molecular engineering utilizing DFT/TD-DFT was employed to calculate the electronic properties of IA-7, including the HOMO/LUMO isosurfaces, the lowest singlet–singlet electronic transitions (E(0–0)), and the ground and excited state oxidation potentials, which were in ideal agreement with the empirical results. The electronic distribution of IA-7 indicated that the HOMO is delocalized not only on Ru and NCS, but also on the substituted TPA, and the LUMO is delocalized over 4,4′-bipyridyl dicarboxylic acid. The Royal Society of Chemistry 2020-01-02 /pmc/articles/PMC9047394/ /pubmed/35492570 http://dx.doi.org/10.1039/c9ra06150a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Abdellah, Islam M. El-Shafei, Ahmed The molecular engineering, synthesis and photovoltaic studies of a novel highly efficient Ru(ii) complex incorporating a bulky TPA ancillary ligand for DSSCs: donor versus π-spacer effects |
title | The molecular engineering, synthesis and photovoltaic studies of a novel highly efficient Ru(ii) complex incorporating a bulky TPA ancillary ligand for DSSCs: donor versus π-spacer effects |
title_full | The molecular engineering, synthesis and photovoltaic studies of a novel highly efficient Ru(ii) complex incorporating a bulky TPA ancillary ligand for DSSCs: donor versus π-spacer effects |
title_fullStr | The molecular engineering, synthesis and photovoltaic studies of a novel highly efficient Ru(ii) complex incorporating a bulky TPA ancillary ligand for DSSCs: donor versus π-spacer effects |
title_full_unstemmed | The molecular engineering, synthesis and photovoltaic studies of a novel highly efficient Ru(ii) complex incorporating a bulky TPA ancillary ligand for DSSCs: donor versus π-spacer effects |
title_short | The molecular engineering, synthesis and photovoltaic studies of a novel highly efficient Ru(ii) complex incorporating a bulky TPA ancillary ligand for DSSCs: donor versus π-spacer effects |
title_sort | molecular engineering, synthesis and photovoltaic studies of a novel highly efficient ru(ii) complex incorporating a bulky tpa ancillary ligand for dsscs: donor versus π-spacer effects |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9047394/ https://www.ncbi.nlm.nih.gov/pubmed/35492570 http://dx.doi.org/10.1039/c9ra06150a |
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