Ruthenium Complexes Bearing Bis‐N‐heterocyclic Carbene Donors in TiO2 Sensitization for Dye‐Sensitized Solar Cells (original) (raw)

European Journal of Inorganic Chemistry

Abstract

This report presents ruthenium (II) complexes featuring bis‐imidazole‐2‐ylidene donors and carboxylic acid‐functionalized terpyridine ligands (tpy−COOH or tpy4′−phenyl−COOH). We introduced the monodentate −NCS or pyridine carboxylate ligands into the coordination sphere to render sizeable changes in photo‐functional attributes. The coordination of the thiocyanate ligands to these ruthenium centers extends their absorption tails up to 800 nm. In contrast, the absorption bands of complexes featuring isonicotinic acid last only until 600 nm. Even though phenyl spacers at the acceptor end rendered a bathochromic shift in the λmax, in their absence, complexes exhibited a longer electron lifetime at the TiO2 photoanode. The complexes devoid of phenyl spacers show lower charge transfer resistance at the TiO2/electrolyte interface giving improved photon conversion efficiency (PCE) in Dye‐Sensitized Solar Cells (DSSCs). Herein, we analyze the relationship between the structure and the light‐...

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