Angewandte Chemie International Edition · 2011 · 260 citations · 24 references
Natural SciencesChemistryPhysicsOptical MaterialsOrganic ChemistrySupramolecular ChemistryOrganic Electronic MaterialsOrganic SemiconductorsPhotovoltaic DevicesPhotovoltaic MaterialsSolar Cell MaterialsSupramolecular MaterialsBulk Heterojunction Solar CellsHeterojunction Solar CellsMolecular ChromophoresOrganic Photovoltaic CellsOrganic PhotovoltaicsOrganic Solar CellsStructure-property Relationships In DyesSupramolecular Interactions
Abstract A series of dipolar donor–acceptor ( D –A) chromophores with aminothiophene donor and different heterocyclic acceptor units is reported. By modulation of the acceptor strength, absorption bands over the whole visible spectrum are accessible as well as adjustment of the frontier molecular orbital levels. The performance of the chromophores in blends with fullerene acceptors in solution‐processed bulk heterojunction solar cells was studied and related to the molecular properties of the dyes. In particular, the effect of the large ground‐state dipole moments of these dyes was investigated by single crystal X‐ray analysis, which revealed antiparallel dimers, resulting in an annihilation of the dipole moments. This specific feature of supramolecular organization explains the excellent performance of merocyanine dyes in organic solar cells. With blends of HB366 :PC 71 BM, the most efficient solar cell with a V OC of 1.0 V, a J SC of 10.2 mA cm −2 , and a power‐conversion efficiency of 4.5 % was achieved under standard AM1.5, 100 mW cm −2 conditions. Under reduced lighting conditions, even higher efficiencies up to 5.1 % was obtained.
24
Organic photovoltaics: a chemical approach
Juan Luis Delgado, Pierre‐Antoine Bouit, Salvatore Filippone et al. · Chemical Communications · 2010 · 373 citations · Full text