Abstract
The photoelectrochemical effects of a series of phenylalkanoic acids as co-adsorbents along with a ruthenium sensitizer, cis-diisothiocyanato-bis(2,2)-bipyridyl-4,4-dicarboxylato) ruthenium(II) bistetrabutylammonium dye (N719), were investigated in dye-sensitized solar cells (DSSCs). All the co-adsorbents used in this study enhanced the short circuit current density (Jsc) resulting from the increased electron injection efficiency due to the significant reduction of dye-aggregation, and this enhancement increased with increasing chain-length of their hydrophobic alkyl groups. They suppressed interfacial back electron transfer rate from the conduction band of TiO2 to triiodide (I? 3) in electrolyte without shifting the quasi-Fermi level of the TiO2 in general, and induced a longer recombination lifetime This corresponded to the enhancement of the open circuit voltage (Voc) of the cells by up to ca. 20 mV compared to that with no co-adsorbents. On the contrary, the photovoltage decreased by ca. 10 mV when 2-phenylethanoic acid was used as a co-adsorbent, which was attributed to the negative shift of the quasi-Fermi level of the TiO2 nanoparticles.
| Original language | English |
|---|---|
| Pages (from-to) | 7880-7885 |
| Number of pages | 6 |
| Journal | Journal of Nanoscience and Nanotechnology |
| Volume | 13 |
| Issue number | 12 |
| DOIs | |
| State | Published - Dec 2013 |
Keywords
- Back Electron Transfer Rate
- Co-Adsorbents
- Dye-Sensitized Solar Cell
- Phenylalkanoic Acids
- Quasi-Fermi Level
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