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Macromolecules
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On the Birefringence of Multilayered Symmetric Diblock Copolymer Films

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Abstract

The chain extension at lamellar interfaces was studied in thin films of symmetric diblock copolymers on gold substrates. The first copolymer consisted of blocks of polystyrene (PS) and poly(2-vinylpyridine) (P2VP), denoted P(S-b-2VP). The second was a diblock copolymer of PS and poly(methyl methacrylate) (PMMA), denoted P(S-b-MMA), on a gold substrate. Using attenuated total reflectance spectroscopy, the refractive indices parallel, n∥, and perpendicular, n⊥, to the surface of the films were determined. It was found that the total birefringence, ΔT = n⊥ − n∥, of the as-cast films was positive, indicative of an orientation of the copolymer chains parallel to the film surface. Upon annealing at 170 °C, ΔT changed sign and attained a limiting value, ∼−7 × 10−4 for P(S-b-2VP) and ∼−20 × 10−4 for P(S-b-MMA). It was found that the form birefringence, ΔF, dominates the intrinsic birefringence, ΔI, for P(S-b-MMA). On the other hand, ΔI was much greater than ΔF for P(S-b-2VP). From ΔI the extension ratios of the chains at the interface were found to be 1.5–1.6 for both copolymers. © 1993, American Chemical Society. All rights reserved.

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Macromolecules

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