Macromolecules · 2016 · 28 citations · 49 references
Natural SciencesMaterials EngineeringMaterials ScienceMaterials ChemistryPolymer ChemistryPolymer MaterialsPolymer CharacterizationPolymer Physical ChemistryPolymer PhysicsPolymer StructurePolymer Thin FilmsPolymeric NanomaterialsAmbipolar TransportCharge TransportFullerenesGlass TransitionGlass Transition TemperatureGrafting DensityMicrophase SeparationOrganic Field-effect Transistors
A series of tailor-made poly(3-hexylthiophene)- block -PPCBM (P3HT- b -PPCBM) block copolymers incorporating P3HT as donor and a polystyrene with pendant fullerenes (PC 61 BM) as acceptor block (PPCBM) is presented. The grafting density of PC 61 BM was varied between 26 and 60 wt %. This has high impact on structure formation, molecular dynamics, and charge transport. It causes considerable increase in glass transition temperature ( T g from 150 to 200 °C). The T g of the amorphous PPCBM block restricts the dynamics of structure evolution of the block copolymer resulting in an incomplete microphase separation, although structural studies revealed a donor–acceptor nanostructure of 30–40 nm in bulk and thin films. All block copolymers exhibit ambipolar charge transport in organic field-effect transistors. Further, the most densely grafted system showed 2 orders of magnitude higher electron mobility. Thus, the fullerene grafting density turned out as a key parameter in designing P3HT- b -PPCBM systems for tuning phase separation and charge transport.
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Conjugated Polymer Photovoltaic Cells
Kevin M. Coakley, Michael D. McGehee · Chemistry of Materials · 2004 · 2.1K citations
Natural Sciences, Materials Engineering, Materials Science +17
Unifying Weak- and Strong-Segregation Block Copolymer Theories
M. W. Matsen, Frank S. Bates · Macromolecules · 1996 · 1.8K citations