Methoxy-substituted copper complexes as possible redox mediators in dye-sensitized solar cells
Three aromatic diimine ligands and the corresponding homoleptic copper(i) and copper(ii) complexes have been synthesized and characterized. The copper(ii) derivatives are stabilized by an ancillary chlorido ligand. The nature of the chelating ligand seriously impacts the photophysical and electroche...
Uloženo v:
| Vydáno v: | New journal of chemistry Ročník 45; číslo 34; s. 15303 - 15311 |
|---|---|
| Hlavní autoři: | , , , , , |
| Médium: | Journal Article |
| Jazyk: | angličtina |
| Vydáno: |
CAMBRIDGE
Royal Soc Chemistry
14.09.2021
|
| Témata: | |
| ISSN: | 1144-0546, 1369-9261 |
| On-line přístup: | Zjistit podrobnosti o přístupu |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
|
| Shrnutí: | Three aromatic diimine ligands and the corresponding homoleptic copper(i) and copper(ii) complexes have been synthesized and characterized. The copper(ii) derivatives are stabilized by an ancillary chlorido ligand. The nature of the chelating ligand seriously impacts the photophysical and electrochemical properties of the complexes. The substitution of the pendant methyl groups with methoxy influences the coordination geometry of the complexes, resulting in an intramolecular dynamic equilibrium between different coordination modes (i.e. nitrogen and oxygen binding), proved by variable-temperature H-1-NMR measurements. As a proof of concept, the most promising complexes were employed as redox mediators in semi-transparent dye-sensitized solar cells. Once implemented in devices, the nature of the ligand plays a crucial role: the methoxy-substituted derivatives appear upon severe ligand exchange with tert-butylpyridine, resulting in an unexpectedly high open circuit voltage. |
|---|---|
| ISSN: | 1144-0546 1369-9261 |
| DOI: | 10.1039/d1nj02577e |