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Can Ferroelectricity Improve Organic Solar Cells?
Author(s) -
AbduAguye Mustapha,
Doumon Nutifafa Y.,
Terzic Ivan,
Dong Jingjin,
Portale Giuseppe,
Loos Katja,
Koster L. Jan Anton,
Loi Maria Antonietta
Publication year - 2020
Publication title -
macromolecular rapid communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 154
eISSN - 1521-3927
pISSN - 1022-1336
DOI - 10.1002/marc.202000124
Subject(s) - materials science , copolymer , ferroelectricity , organic solar cell , ferroelectric polymers , polymer solar cell , polymer , energy conversion efficiency , chemical engineering , polymer chemistry , thin film , dielectric , nanotechnology , optoelectronics , composite material , engineering
Blends of semiconducting (SC) and ferroelectric (FE) polymers have been proposed for applications in resistive memories and organic photovoltaics (OPV). For OPV, the rationale is that the local electric field associated with the dipoles in a blend could aid exciton dissociation, thus improving power conversion efficiency. However, FE polymers either require solvents or processing steps that are incompatible with those required for SC polymers. To overcome this limitation, SC (poly(3‐hexylthiophene)) and FE (poly(vinylidene fluoride‐trifluoroethylene)) components are incorporated into a block copolymer and thus a path to a facile fabrication of smooth thin films from suitably chosen solvents is achieved. In this work, the photophysical properties and device performance of organic solar cells containing the aforementioned block copolymer consisting of poly(vinylidene fluoride‐trifluoroethylene): P(VDF‐TrFE), poly(3‐hexylthiophene): P3HT and the electron acceptor phenyl‐C 61 ‐butyric acid methyl ester: [60]PCBM are explored. A decrease in photovoltaic performance is observed in blends of the copolymer with P3HT:[60]PCBM, which is attributed to a less favorable nanomorphology upon addition of the copolymer. The role of lithium fluoride (the cathode modification layer) is also clarified in devices containing the copolymer, and it is demonstrated that ferroelectric compensation prevents the ferroelectricity of the copolymer from improving photovoltaic performance in SC‐FE blends.