Abstract
A series of new donor–acceptor organic sensitizers LJ5–LJ7 assembled with isoxazole or its derivative 3-oxopropanenitrile was synthesized and used in dye-sensitized solar cells to study the effect of both π-spacers and anchoring groups on device performance. X-ray crystal structure analyses show planar arrangement of dithiophene and isoxazole fragments, providing an excellent π conjugation and hence the large electronic coupling between the triphenylamine donor and electron acceptor units. For the DSSC applications, the derived photophysical and photovoltaic properties revealed a lower η value of 1.06% (LJ7) and 2.41% (LJ5), and 3.30% (LJ7) for the dyes with rhodanine-3-acetic acid, cyanoacetyl group, and vinyl cyanoacetic acid as the anchor. Electrochemical impedance spectroscopy was used to determine the interfacial charge transfer process occurring in solar cells that employed different dyes.
| Original language | English |
|---|---|
| Pages (from-to) | 4223-4229 |
| Journal | Tetrahedron |
| Volume | 66 |
| Issue number | 23 |
| Online published | 27 Mar 2010 |
| DOIs | |
| Publication status | Published - 5 Jun 2010 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Research Keywords
- Dye-sensitized solar cell
- Dithiophene
- Isooxazole
- Cyanoacetic acid
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