Abstract
Four novel D-D-π-A type organic dyes (DWH1-DWH4) were designed and synthesized, in which 3,6-bis(thiophene or hexylthiophene)-disubstituted carbazole moieties were used as the electron donor, bithiophene units or their derivatives as the π-conjugated bridge, and a cyanoacrylic acid group as the electron acceptor. The photovoltaic performance data indicate that the tuning of the Jsc and Voc values can be conveniently accomplished by incorporation of long alkyl chains into sensitizer, which not only improves the molar extinction coefficients of the absorption and enhances the solubility but also increases the electron lifetime by leading to an effective spatial separation of the charges.
| Original language | English |
|---|---|
| Pages (from-to) | 18-23 |
| Number of pages | 6 |
| Journal | Dyes and Pigments |
| Volume | 114 |
| Issue number | C |
| DOIs | |
| State | Published - Mar 2015 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 7 Affordable and Clean Energy
Keywords
- Carbazole
- Dye-sensitized solar cells
- Organic dye
- Photovoltaic performance
- The hexyl chain
- Thiophene
Fingerprint
Dive into the research topics of 'Novel carbazole based sensitizers for efficient dye-sensitized solar cells: Role of the hexyl chain'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver