Advanced Functional Materials · 2012 · 182 citations · 43 references
Natural SciencesChemistryMaterials ScienceElectronic MaterialsSemiconductor MaterialsThin FilmsCrystal GrowthOrganic Electronic MaterialsOrganic SemiconductorsSemiconductor Crystal GrowthSemiconductor Device MaterialsThin-film MaterialsCrystal Growth MechanismsCrystallinityCrystallizationCrystallization BehaviorCrystallization In Thin FilmsOrganic ElectronicsOrganic Field-effect TransistorsOrganic Thin Films
Abstract The preparation of uniform large‐area highly crystalline organic semiconductor thin films that show outstanding carrier mobilities remains a challenge in the field of organic electronics, including organic field‐effect transistors. Quantitative control over the drying speed during dip‐coating permits optimization of the organic semiconductor film formation, although the kinetics of crystallization at the air–solution–substrate contact line are still not well understood. Here, we report the facile one‐step growth of self‐aligning, highly crystalline soluble acene crystal arrays that exhibit excellent field‐effect mobilities (up to 1.5 cm V −1 s −1 ) via an optimized dip‐coating process. We discover that optimized acene crystals grew at a particular substrate lifting‐rate in the presence of low boiling point solvents, such as dichloromethane (b.p. of 40.0 °C) or chloroform (b.p. of 60.4 °C). Variable‐temperature dip‐coating experiments using various solvents and lift rates are performed to elucidate the crystallization behavior. This bottom‐up study of soluble acene crystal growth during dip‐coating provides conditions under which one may obtain uniform organic semiconductor crystal arrays with high crystallinity and mobilities over large substrate areas, regardless of the substrate geometry (wafer substrates or cylinder‐shaped substrates).
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Capillary flow as the cause of ring stains from dried liquid drops
Robert D. Deegan, Olgica Bakajin, Todd F. Dupont et al. · Nature · 1997 · 6.3K citations