Abstract
A series of ruthenium photosensitizers incorporating a β-diketonate non-innocent ligand were synthesized, characterized, and implemented in dye-sensitized solar cells. Electrochemical studies exhibited well behaved reversible oxidations and reductions for all β-diketonate complexes. The acac- and Ph2acac- based photosensitizers possess limited delocalization across the ligand π∗-manifold, which is significant for exhibition of respectable power conversion efficiencies in a dye-sensitized solar cell (DSC) device. As the π-orbital network was extended on the flavone and curcumin inspired NILs, increased molar absorptivity was observed, however this ultimately proved detrimental to DSC performance consistent with exhibition of negligible photocurrent.
| Original language | English |
|---|---|
| Pages (from-to) | 16516-16524 |
| Number of pages | 9 |
| Journal | Physical Chemistry Chemical Physics |
| Volume | 23 |
| Issue number | 31 |
| DOIs | |
| State | Published - Aug 21 2021 |
ASJC Scopus Subject Areas
- General Physics and Astronomy
- Physical and Theoretical Chemistry
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