Abstract
A new donor-acceptor copolymer system based upon a dithienopyrrole (DTP) donor moiety and a thienopyrrolodione (TPD) accepting moiety has been designed and synthesized for organic photovoltaic (OPV) applications. The TPD accepting moiety has recently gained significant attention in the OPV community and is being incorporated into a number of different polymer systems. In contrast, the DTP donormoiety has received only limited attention, likely due in part to synthetic difficulties relating to the monomer. In our hands, the bis(trimethyltin)-DTP monomer was indelibly contaminated with~5% of the mono-destannylated DTP, which limited the Stille polymerization with the dibromo-TPD monomer (>99% pure) to produce material with Mn~4130 g/mol (PDI = 1.10), corresponding to around eightrepeat units. Despite this limitation, UV-visible absorption spectroscopy demonstrates strong absorption for this material with a band gap of~1.6 eV. Cyclic voltammetry indicates a highest occupied molecular orbital (HOMO) energy level of -5.3 eV, which is much lower than calculations predicted. Initial bulk heterojunction OPV devices fabricated with the fullerene acceptor phenyl C61 butyricacid methyl ester (PCBM) exhibit Voc~700 mV, which supports the deep HOMO value obtained from CV. These results suggest the promise of this copolymer system.
Original language | American English |
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Number of pages | 6 |
State | Published - 2011 |
Event | 37th IEEE Photovoltaic Specialists Conference (PVSC 37) - Seattle, Washington Duration: 19 Jun 2011 → 24 Jun 2011 |
Conference
Conference | 37th IEEE Photovoltaic Specialists Conference (PVSC 37) |
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City | Seattle, Washington |
Period | 19/06/11 → 24/06/11 |
NREL Publication Number
- NREL/CP-5200-50660
Keywords
- DTP
- DTP-TPD
- OPV
- organic photovoltaics
- TRP