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Synthesis and DSSC application of BODIPY decorated triazole bridged and benzene nucleus cored conjugated dendrimers

Conjugated dendrimers decorated with 5,5-difluoro-10-(4-(prop-2-ynyloxy)phenyl)-5H-dipyrrolo[1,2-c:1′,2′-f][1,3,2]diazaborinin-4-ium-5-uide, usually known as boron dipyrromethene (BODIPY), have been synthesized and their application as photosensitizer in dye sensitized solar cells (DSSCs) has been e...

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Autores principales: Saravanan, Velautham, Ganesan, Shanmugam, Rajakumar, Perumal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9053714/
https://www.ncbi.nlm.nih.gov/pubmed/35517187
http://dx.doi.org/10.1039/d0ra01672a
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author Saravanan, Velautham
Ganesan, Shanmugam
Rajakumar, Perumal
author_facet Saravanan, Velautham
Ganesan, Shanmugam
Rajakumar, Perumal
author_sort Saravanan, Velautham
collection PubMed
description Conjugated dendrimers decorated with 5,5-difluoro-10-(4-(prop-2-ynyloxy)phenyl)-5H-dipyrrolo[1,2-c:1′,2′-f][1,3,2]diazaborinin-4-ium-5-uide, usually known as boron dipyrromethene (BODIPY), have been synthesized and their application as photosensitizer in dye sensitized solar cells (DSSCs) has been evaluated. Third generation triazole bridged BODIPY dendrimers show higher light energy harvesting efficiency of 2.5% better than the first and second generation dendrimers, when used as a dye material in solar cells. The current intensity increases with an increase in the generation of the dendrimer as revealed by cyclic voltammetry. Fluorescence decay analysis shows that the relaxation times τ(1) and τ(2) increase as the dendrimer generation increases, however τ(2) for the third generation dendrimer decreases because of fluorescence quenching due to molecular crowding.
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spelling pubmed-90537142022-05-04 Synthesis and DSSC application of BODIPY decorated triazole bridged and benzene nucleus cored conjugated dendrimers Saravanan, Velautham Ganesan, Shanmugam Rajakumar, Perumal RSC Adv Chemistry Conjugated dendrimers decorated with 5,5-difluoro-10-(4-(prop-2-ynyloxy)phenyl)-5H-dipyrrolo[1,2-c:1′,2′-f][1,3,2]diazaborinin-4-ium-5-uide, usually known as boron dipyrromethene (BODIPY), have been synthesized and their application as photosensitizer in dye sensitized solar cells (DSSCs) has been evaluated. Third generation triazole bridged BODIPY dendrimers show higher light energy harvesting efficiency of 2.5% better than the first and second generation dendrimers, when used as a dye material in solar cells. The current intensity increases with an increase in the generation of the dendrimer as revealed by cyclic voltammetry. Fluorescence decay analysis shows that the relaxation times τ(1) and τ(2) increase as the dendrimer generation increases, however τ(2) for the third generation dendrimer decreases because of fluorescence quenching due to molecular crowding. The Royal Society of Chemistry 2020-05-13 /pmc/articles/PMC9053714/ /pubmed/35517187 http://dx.doi.org/10.1039/d0ra01672a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Saravanan, Velautham
Ganesan, Shanmugam
Rajakumar, Perumal
Synthesis and DSSC application of BODIPY decorated triazole bridged and benzene nucleus cored conjugated dendrimers
title Synthesis and DSSC application of BODIPY decorated triazole bridged and benzene nucleus cored conjugated dendrimers
title_full Synthesis and DSSC application of BODIPY decorated triazole bridged and benzene nucleus cored conjugated dendrimers
title_fullStr Synthesis and DSSC application of BODIPY decorated triazole bridged and benzene nucleus cored conjugated dendrimers
title_full_unstemmed Synthesis and DSSC application of BODIPY decorated triazole bridged and benzene nucleus cored conjugated dendrimers
title_short Synthesis and DSSC application of BODIPY decorated triazole bridged and benzene nucleus cored conjugated dendrimers
title_sort synthesis and dssc application of bodipy decorated triazole bridged and benzene nucleus cored conjugated dendrimers
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9053714/
https://www.ncbi.nlm.nih.gov/pubmed/35517187
http://dx.doi.org/10.1039/d0ra01672a
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