TY - JOUR
T1 - A small molecule non-fullerene electron acceptor for organic solar cells
AU - Schwenn, Paul E.
AU - Gui, K.
AU - Nardes, Alexandre M.
AU - Krueger, Karsten B.
AU - Lee, Kwan H.
AU - Mutkins, Karyn
AU - Rubinstein-Dunlop, Halina
AU - Shaw, Paul E.
AU - Kopidakis, Nikos
AU - Burn, Paul L.
AU - Meredith, Paul
PY - 2011/1/1
Y1 - 2011/1/1
N2 - Organic bulk heterojunction photovoltaic devices predominantly use the fullerene derivatives [C60]PCBM and [C70]PCBM as the electron accepting component. This report presents a new organic electron accepting small molecule 2-[{7-(9,9-di- -propyl-9 -fl uoren-2-yl)benzo[c][1,2,5]thiadiazol-4-yl} methylene]malononitrile (K12) for organic solar cell applications. It can be processed by evaporation under vacuum or by solution processing to give amorphous thin films and can be annealed at a modest temperature to give films with much greater order and enhanced charge transport properties. The molecule can efficiently quench the photoluminescence of the donor polymer poly(3- -hexylthiophene-2,5-diyl) (P3HT) and time resolved microwave conductivity measurements show that mobile charges are generated indicating that a truly charge separated state is formed. The power conversion efficiencies of the photovoltaic devices are found to depend strongly on the acceptor packing. Optimized K12:P3HT bulk heterojunction devices have efficiencies of 0.73 ± 0.01% under AM1.5G simulated sunlight. The efficiencies of the devices are limited by the level of crystallinity and nanoscale morphology that was achievable in the blend with P3HT.
AB - Organic bulk heterojunction photovoltaic devices predominantly use the fullerene derivatives [C60]PCBM and [C70]PCBM as the electron accepting component. This report presents a new organic electron accepting small molecule 2-[{7-(9,9-di- -propyl-9 -fl uoren-2-yl)benzo[c][1,2,5]thiadiazol-4-yl} methylene]malononitrile (K12) for organic solar cell applications. It can be processed by evaporation under vacuum or by solution processing to give amorphous thin films and can be annealed at a modest temperature to give films with much greater order and enhanced charge transport properties. The molecule can efficiently quench the photoluminescence of the donor polymer poly(3- -hexylthiophene-2,5-diyl) (P3HT) and time resolved microwave conductivity measurements show that mobile charges are generated indicating that a truly charge separated state is formed. The power conversion efficiencies of the photovoltaic devices are found to depend strongly on the acceptor packing. Optimized K12:P3HT bulk heterojunction devices have efficiencies of 0.73 ± 0.01% under AM1.5G simulated sunlight. The efficiencies of the devices are limited by the level of crystallinity and nanoscale morphology that was achievable in the blend with P3HT.
UR - http://www.scopus.com/inward/record.url?scp=84863230659&partnerID=8YFLogxK
UR - http://purl.org/au-research/grants/arc/FF0668728
UR - http://purl.org/au-research/grants/arc/DP0879194
U2 - 10.1002/aenm.201000024
DO - 10.1002/aenm.201000024
M3 - Article
AN - SCOPUS:84863230659
VL - 1
SP - 73
EP - 81
JO - Advanced Energy Materials
JF - Advanced Energy Materials
SN - 1614-6832
IS - 1
ER -