Abstract
Dye-sensitized solar Cells have attracted great attention recently due to their excellent advantages. This study introduces the cobalt and zinc metal complexes as a new class of sensitizers for evaluation. We report the synthesis and characterization of zinc and cobalt complexes of organic dyes and applications of Dye-Sensitive TiO2 Solar Cells. In this study, the reason we prefer cobalt and zinc complexes is that they provide a wide absorption spectrum and high molar absorption. The fact that these complexes have good energy level adaptations helps in efficient electron transfer. In the designed complexes, 4,5-diazafluoren metal complexes bonded with thiophene and carbonyl as electron donors and as electron-with drawing groups were synthesized. Structural characterization was achieved with FTIR, UV-Vis, and Maldi-MS. The metal complex binder dye has demonstrated promising DSSC properties such as short-circuit current, open-circuit voltage, and fill factor, indicating efficient charge generation and injection. The bathochromic shift seen in the UV-Vis spectra of the dyes was promising for good efficiency. Notably, the highest efficiency was obtained from ZnS2 with 0.61%, while the lowest was from CoS1 with 0.17%. The power conversion efficiencies (η) produced by CoS1, CoS2, ZnS1, and ZnS2 dyes exhibit device performance ZnS2 > ZnS1 > CoS2 > CoS1 respectively. With these results, the development of DSSCs is promising.
This is a visual representation of the abstract.
Keywords
Get full access to this article
View all access options for this article.
References
Supplementary Material
Please find the following supplemental material available below.
For Open Access articles published under a Creative Commons License, all supplemental material carries the same license as the article it is associated with.
For non-Open Access articles published, all supplemental material carries a non-exclusive license, and permission requests for re-use of supplemental material or any part of supplemental material shall be sent directly to the copyright owner as specified in the copyright notice associated with the article.
