Diblock copolymer ordering induced by patterned surfaces
arXiv:cond-mat/0007056 · doi:10.1209/epl/i2001-00211-3
Abstract
We use a Ginzburg-Landau free energy functional to investigate diblock copolymer morphologies when the copolymer melt interacts with one surface or is confined between two chemically patterned surfaces. For temperatures above the order-disorder transition a complete linear response description of the copolymer melt is given, in terms of an arbitrary two-dimensional surface pattern. The appearance of order in the direction parallel to the surface is found as a result of the order in the perpendicular direction. Below the order-disorder point and in a thin-film geometry, our procedure enables the analytic calculation of distorted perpendicular and tilted lamellar phases in the presence of uniform or modulated surface fields.
8 pages, 3 figures, to be published in Europhys. Lett
References in corpus (6)
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Cited by in corpus (9)
- Phase-field-crystal models for condensed matter dynamics on atomic length and diffusive time scales: an overview
- Thin Film Diblock Copolymers in Electric Field: Transition from Perpendicular to Parallel Lamellae
- Structural changes in block copolymers: coupling of electric field and mobile ions
- Surface induced ordering in thin film diblock copolymers: tilted lamellar phases
- Forces between chemically structured substrates mediated by critical fluids
- Block Copolymer at Nano-Patterned Surfaces
- Coarse Graining in Block Copolymer Films
- Interfacial Phenomena of Solvent-diluted Block Copolymers
- Phase lines in mean-field models with nonuniform external forces