Nonbulk Complex Structures in Thin Films of Symmetric Block Copolymers on Chemically Nanopatterned Surfaces
Thin films of symmetric polystyrene-block-poly(methyl methacrylate) (PS-b-PMMA) with a bulk lamellar period of L o were equilibrated on chemically nanopatterned surfaces that had alternating PS and PMMA preferential wetting stripes. The chemical patterns had a period of L S , and the width of the PM...
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Veröffentlicht in: | Macromolecules 2012-05, Vol.45 (9), p.3986-3992 |
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Sprache: | eng |
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Zusammenfassung: | Thin films of symmetric polystyrene-block-poly(methyl methacrylate) (PS-b-PMMA) with a bulk lamellar period of L o were equilibrated on chemically nanopatterned surfaces that had alternating PS and PMMA preferential wetting stripes. The chemical patterns had a period of L S , and the width of the PMMA wetting stripes was W. We identified a set of four morphologies, two of which are fully three-dimensional. On chemical patterns with L S = 2L o , as W/L 0 increased from 0 to 1, block copolymers formed morphologies including bulk-like structures, nominally, parallel lamellae and vertical lamellae, and two bulk-deviate complex morphologies. On chemical patterns with W/L 0 = 0.5, as the commensurability factor, δ = L S/L 0, increased from 0.87 to 3.05, block copolymers formed complex three-dimensional structures. At the substrate, the block copolymer had a wetting layer reflecting the chemical pattern. At the free surface, the block copolymer formed lamellar-like structures with period L 0 along the direction of the underlying chemically patterned stripes when δ was close to an integer, and fingerprint-like structures when δ was not close to an integer. Morphologies obtained by numerical simulations of a coarse grained model of block copolymers compare favorably with our experimental results and help explain the origin of the observed behavior. |
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ISSN: | 0024-9297 1520-5835 |
DOI: | 10.1021/ma202777s |