Proceedings of 6th International Conference on Hybrid and Organic Photovoltaics (HOPV14)
Publication date: 1st March 2014
Many diketopyrrolopyrrole based polymers feature an additional low energy shoulder next to the main absorption peak in the UV/vis absorption spectra. We show that this additional shoulder is due to homo-coupling defects originating from a side reaction of the DPP2TBr2 monomers used in the palladium catalyzed polymerization reaction. PDPPTPT has been used as a model system to investigate the influence of these homo-coupling defects on the photovoltaic performance. We have compared polymers that were synthesized with optimal and suboptimal reaction conditions, yielding polymers with and without defects. Additionally, polymers were synthesized where a fixed amount of homo-coupled (DPP2T)2Br2 monomer was introduced to the reaction mixture, whilst using optimal conditions. The resulting defects effectively decrease the LUMO and increase the HOMO energy levels of the material, and can act as low lying energy trap sites, inhibiting exciton dissociation. This reduces the photocurrent that can be obtained from solar cells when combined with [70]PCBM and leads to a significant reduction of the PCE from 7.5% all the way down to 2.9%, depending on the amount of defects present. It is very likely that other DPP based polymers published in literature which display the long wavelength shoulder suffer from the same type of defects and resulting performance loss. It shows that a relative small amount of defects can have a detrimental effect on the photovoltaic performance and the importance of carefully optimizing reaction conditions in order to obtain high performing, defect free, polymers.
Formation of homo-coupling defects in PDPPTPT
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