Superlattice formation in binary mixtures of block copolymer micelles

Sayeed Abbas, Timothy P. Lodge

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

Two distinct diblock copolymers, poly(styrene-b-isoprene) (SI) and poly(styrene-b-dimethylsiloxane) (SD), were codissolved at various concentrations in the polystyrene selective solvent diethyl phthalate. Two SI diblocks, with block molar masses of 12 000-33 000 and 30 000-33 000, and two SD diblocks, with block molar masses of 19 000-6000 and 16 000-9000, were employed. The size ratio of the smaller SD micelles (S) to the larger SI micelles (L) varied from approximately 0.5 to 0.6, based on hydrodynamic radii determined by dynamic light scattering on dilute solutions containing only one polymer component. Due to incompatibility between the polyisoprene and polydimethylsiloxane blocks, a binary mixture of distinct SI and SD micelles was formed in each mixed solution, as confirmed by cryogenic transmission electron microscopy. When the total concentration of polymer was increased to 20-30%, the micelles adopted a superlattice structure. Small angle X-ray scattering revealed the lattice to be the full LS13 superlattice (space group Fm3̄c) in all cases, with unit cell dimensions in excess of 145 nm. A coexistent face-centered cubic phase composed of SD micelles was also observed when the number ratio of S to L micelles was large.

Original languageEnglish (US)
Pages (from-to)6247-6253
Number of pages7
JournalLangmuir
Volume24
Issue number12
DOIs
StatePublished - Jun 17 2008

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