Self-assembly of symmetric brush diblock copolymers

Weiyin Gu, June Huh, Sung Woo Hong, Benjamin R. Sveinbjornsson, Cheolmin Park, Robert Howard Grubbs, Thomas P. Russell

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75 Citations (Scopus)

Abstract

Self-assembled structures of brush block copolymers (BrBCPs) with polylactide (PLA) and polystyrene (PS) side chains were studied. The polynorbornene-backbone-based BrBCPs containing approximately equal volume fractions of each block self-assembled into highly ordered lamellae with domain spacing ranging from 20 to 240 nm by varying molecular weight of the backbone in the bulk state, as revealed by small-angle X-ray scattering (SAXS). The domain size increased approximately linearly with backbone length, which indicated an extended conformation of the backbone in the ordered state. In situ SAXS measurements suggested that the BrBCPs self-assemble with an extremely fast manner which could be attributed to a reduced number of entanglements between chains. The strong segregation theory and Monte Carlo simulation also confirmed this near-linear dependence of the domain spacing on backbone length, rationalizing experimental results.

Original languageEnglish
Pages (from-to)2551-2558
Number of pages8
JournalACS Nano
Volume7
Issue number3
DOIs
Publication statusPublished - 2013 Mar 26

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All Science Journal Classification (ASJC) codes

  • Materials Science(all)
  • Engineering(all)
  • Physics and Astronomy(all)

Cite this

Gu, W., Huh, J., Hong, S. W., Sveinbjornsson, B. R., Park, C., Grubbs, R. H., & Russell, T. P. (2013). Self-assembly of symmetric brush diblock copolymers. ACS Nano, 7(3), 2551-2558. https://doi.org/10.1021/nn305867d