Publication | Closed Access
Alkylated-C60 based soft materials: regulation of self-assembly and optoelectronic properties by chain branching
63
Citations
57
References
2013
Year
EngineeringOrganic Solar CellMolecular Self-assemblyMaterial InnovationC60-based MaterialsChemistrySoft MatterChain BranchingPhotovoltaicsPolymersLiquid FullerenesFullereneSoft MaterialsHybrid MaterialsCompound 1Polymer ChemistryMaterials ScienceSolar PowerOptoelectronic PropertiesOptoelectronic MaterialsOrganic SemiconductorElectronic MaterialsOrganic-inorganic Hybrid MaterialNatural SciencesSelf-assemblyPolymer ScienceApplied PhysicsSolar CellsFunctional MaterialsSolar Cell Materials
Derivatization of fullerene (C60) with branched aliphatic chains softens C60-based materials and enables the formation of thermotropic liquid crystals and room temperature nonvolatile liquids. This work demonstrates that by carefully tuning parameters such as type, number and substituent position of the branched chains, liquid crystalline C60 materials with mesophase temperatures suited for photovoltaic cell fabrication and room temperature nonvolatile liquid fullerenes with tunable viscosity can be obtained. In particular, compound 1, with branched chains, exhibits a smectic liquid crystalline phase extending from 84 °C to room temperature. Analysis of bulk heterojunction (BHJ) organic solar cells with a ca. 100 nm active layer of compound 1 and poly(3-hexylthiophene) (P3HT) as an electron acceptor and an electron donor, respectively, reveals an improved performance (power conversion efficiency, PCE: 1.6 ± 0.1%) in comparison with another compound, 10 (PCE: 0.5 ± 0.1%). The latter, in contrast to 1, carries linear aliphatic chains and thus forms a highly ordered solid lamellar phase at room temperature. The solar cell performance of 1 blended with P3HT approaches that of PCBM/P3HT for the same active layer thickness. This indicates that C60 derivatives bearing branched tails are a promising class of electron acceptors in soft (flexible) photovoltaic devices.
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