Journal
LANGMUIR
Volume 26, Issue 6, Pages 3955-3961Publisher
AMER CHEMICAL SOC
DOI: 10.1021/la903313k
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Funding
- Swiss Federal Office of Energy (BFE) for financial support.
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Supramolecular agglomerates of organic colorants based on noncovalent interactions are promising candidates for the development of sensors, optoelectronics, lighting, or photovoltaics. However, their fast and defect-free fabrication oil large scales using low-cost technologies has proven elusive so far, Here, we introduce a so far unreported mechanism to induce molecular order in cyanine dyes within minutes from organic solvents by self-assembly. Spin coating blends of a cyanine dye and a soluble fullerene derivative ([6,6]-phenyl C-61-butyric acid methyl ester (PCBM)) from apolar, aprotic solvents leads to phase-separated structures oil the micrometer scale. With this superordinated phase structure, adjustment of dye aggregation is possible, leading to novel optical properties of the film emerging from dye self-assembly on the nanometer scale. In the primary process, semiporous PCBM domains act as nucleation sites for H-aggregates. H-aggregates can then be reconstructed into J-aggregates by dissolving PCBM from the film. Unexpectedly, the method even works for sterically hindered cyanine dyes that are known for their reduced tendency to aggregate. Additionally, selective removal of H-aggregates leaves a template of PCBM nanocrystals, onto which cyanine dye monomers readsorb from solution, forming H-aggregates of similar quality,
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