From Molecular Design to Co-sensitization; High performance indole based photosensitizers for dye-sensitized solar cells
| dc.contributor.author | Babu, D.D. | |
| dc.contributor.author | Su, R. | |
| dc.contributor.author | El-Shafei, A. | |
| dc.contributor.author | Vasudeva Adhikari, A.V. | |
| dc.date.accessioned | 2026-02-05T09:33:13Z | |
| dc.date.issued | 2016 | |
| dc.description.abstract | Herein, we report the molecular design and synthesis of two novel organic co-adsorbers DBA-1((Z)-2-cyano-3-(5-(4-(cyclohexa-1,5-dien-3-ynyl(phenyl)amino)phenyl)-1-hexyl-1H-indol-3-yl)acrylic acid) and (DBA-2) 5-((5-(4-(diphenylamino)phenyl)-1-hexyl-1H-indol-3-yl)methylene)pyrimidine-2,4,6(1H,3H,5H)-trione with D-D-A (donor-donor-acceptor) architecture. We have combined the strong electron donating triphenylamine group with indole moiety attached to different acceptors/anchoring groups, as co-adsorbers for dye-sensitized solar cells and we present for the first time, the role of anchoring/acceptor unit on their co-adsorption properties. In this study, cyanoacetic acid and barbituric acid are employed as anchoring groups in the co-sensitizers DBA-1 and DBA-2, respectively. Their electrochemical and photo-physical properties along with molecular geometries, obtained from Density Functional Theory (DFT) are employed to vindicate the effect of co-sensitizer structures on photovoltaic properties of DSSCs. We have demonstrated that the co-sensitization effect is profoundly dependent upon the anchoring/acceptor unit in the co-adsorber molecule. Devices co-sensitized using DBA-1 and DBA-2 along with HD-2 (Ru-complex of 4, 4?-bis-(1,4-benzodioxan-5-yl-vinyl)-[2,2?]bipyridine), displayed higher power conversion efficiencies (PCEs) than the device sensitized using only HD-2. In the present work, ruthenium based sensitizer, HD-2, has been chosen due to its better solar-to-power conversion efficiency and impressively higher photocurrent densities than that of standard N719. Among them, co-adsorber DBA-2, containing barbituric acid as the acceptor/anchoring group displays promising photovoltaic results and exhibited an enhanced efficiency of 8.06%. Further, good agreement between the calculated and experimental results showcase the precision of the energy functional and basis set utilized in this study. All these findings provide a deeper insight and better understanding into the intricacies involved in the design of superior co-sensitizers for development of highly efficient DSSCs. © 2016 Elsevier Ltd. All rights reserved. | |
| dc.identifier.citation | Electrochimica Acta, 2016, 198, , pp. 10-21 | |
| dc.identifier.issn | 134686 | |
| dc.identifier.uri | https://doi.org/10.1016/j.electacta.2016.03.061 | |
| dc.identifier.uri | https://idr.nitk.ac.in/handle/123456789/26016 | |
| dc.publisher | Elsevier Ltd | |
| dc.subject | Adsorption | |
| dc.subject | Conversion efficiency | |
| dc.subject | Density functional theory | |
| dc.subject | Design for testability | |
| dc.subject | Dyes | |
| dc.subject | Hydrogels | |
| dc.subject | Photosensitizers | |
| dc.subject | Photovoltaic effects | |
| dc.subject | Polycyclic aromatic hydrocarbons | |
| dc.subject | Solar cells | |
| dc.subject | Anchoring groups | |
| dc.subject | indole | |
| dc.subject | Molecular geometries | |
| dc.subject | Photophysical properties | |
| dc.subject | Photovoltaic property | |
| dc.subject | Power conversion efficiencies | |
| dc.subject | Suzuki couplings | |
| dc.subject | Triphenylamine groups | |
| dc.subject | Dye-sensitized solar cells | |
| dc.title | From Molecular Design to Co-sensitization; High performance indole based photosensitizers for dye-sensitized solar cells |
