Abstract
Four organic photosensitizers incorporating a carbazole or 3,6-diiodocarbazole unit as the electron donor, a benzene/thiophene or oligothiophene moiety as the conjugated spacer, and 2-cyanoacrylic acid as the electron acceptor have been synthesized. The photovoltaic performance data are quite sensitive to the structural modification of sensitizer. The introduction of the benzene/thiophene linker benefits from lower tendency to aggregate, but disfavors the electron transport between donor and acceptor. The addition of a thiophene unit in the bridge efficiently red-shifts the absorption response, however, organic dyes have some π-π aggregation. Incorporation of 3,6-diiodocarbazole as a dendritic donor unit not only enhances the molar extinction coefficients of the absorption but also suppresses the charge recombination with electrolyte.
| Original language | English |
|---|---|
| Pages (from-to) | 269-277 |
| Number of pages | 9 |
| Journal | Dyes and Pigments |
| Volume | 100 |
| Issue number | 1 |
| DOIs | |
| State | Published - 2014 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Carbazole
- Dendritic 3,6-diiodocarbazole
- Dye-sensitized solar cells
- Organic dye
- Photovoltaic performance
- Thiophene
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