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Investigation on the coordination between methylpyridine additives and the [Cu(dmp) 2 ] 2+/+ redox couple and its improvement towards the stability of the dye-sensitized solar cells
In dye-sensitized solar cells (DSSCs), the use of copper( ii / i ) complex redox couples enables a high open-circuit voltage of greater than 1.0 V. However, the widely used electrolyte additive, 4- tert -butylpyridine (TBP), poisons the copper( ii ) complex, resulting in poor device stability. In th...
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Published in: | Sustainable energy & fuels 2024-05, Vol.8 (10), p.2256-2264 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | In dye-sensitized solar cells (DSSCs), the use of copper(
ii
/
i
) complex redox couples enables a high open-circuit voltage of greater than 1.0 V. However, the widely used electrolyte additive, 4-
tert
-butylpyridine (TBP), poisons the copper(
ii
) complex, resulting in poor device stability. In this study, a series of pyridine derivatives 2-methylpyridine (2MP), 3-methylpyridine (3MP), 4-methylpyridine (4MP), and 3,5-dimethylpyridine (35DMP) were studied as alternatives to TBP for solving or mitigating the TBP-induced performance degradation. The coordination between the additives and copper(
ii
) complex was extensively studied using ultraviolet-visible spectrophotometric titration, cyclic voltammetry, and
1
H-nuclear magnetic resonance spectroscopy. The moiety position on the pyridine ring was found to greatly affect the electrochemical properties of the redox couple. The 35DMP penta-coordinated copper(
ii
) was found to least affect the electrochemical activity at the counter electrode and ionic diffusion in the bulk electrolyte. A DSSC with a 35DMP additive outperforms its TBP-based counterparts in not only power conversion efficiency but also long-term stability. |
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ISSN: | 2398-4902 2398-4902 |
DOI: | 10.1039/D3SE00983A |