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Morphology Development in Amorphous Polymer:Fullerene Photovoltaic Blend Films During Solution Casting
Author(s) -
Pearson Andrew J.,
Wang Tao,
Dunbar Alan D. F.,
Yi Hunan,
Watters Darren C.,
Coles David M.,
Staniec Paul A.,
Iraqi Ahmed,
Jones Richard A. L.,
Lidzey David G.
Publication year - 2014
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.201301922
Subject(s) - fullerene , materials science , polymer , amorphous solid , casting , chemical engineering , polymer blend , organic solar cell , precipitation , solubility , nanotechnology , composite material , organic chemistry , chemistry , physics , meteorology , engineering , copolymer
The evolution of film structure is reported during solution casting of PCDTBT:PC 70 BM 1:4 wt%, a polymer:fullerene blend system that finds application in an organic photovoltaic device. Using the complimentary techniques of grazing‐incidence wide‐angle X‐ray scattering and spectroscopic ellipsometry, a number of distinct processes that occur during film formation are identified. This includes the growth of fullerene molecules into nanoscale aggregates, the onset of which coincides with the solubility limit of the material in the casting solvent being reached. An apparent delay in Bragg scatter from the PCDTBT‐rich phase of the film suggests that, for the film composition studied here, the aggregation of PC 70 BM precedes weak self‐organisation of the conjugated polymer. This behaviour is compared with the drying dynamics of a number of different polymer:fullerene blends that each contain a high weight fraction of fullerene molecules, and a range of comparable solid concentrations are identified beyond which the precipitation of fullerene aggregates from solution occurs. These observations provide an insight into the development of structure in relatively amorphous polymer:fullerene blends for organic photovoltaic applications and potentially assists the future optimisation of this category of materials.