Self-assembly of an interacting binary blend of diblock copolymers in thin films: A potential route to porous materials with reactive nanochannel chemistry

Jingyi Rao, Huan Ma, Julia Baettig, Sanghoon Woo, Mihaiela C. Stuparu, Joona Bang, Anzar Khan

Research output: Contribution to journalArticlepeer-review

17 Citations (Scopus)

Abstract

Self-assembly of a binary mixture of poly(styrene)336-block- poly(4-vinyl pyridine)25 (PS336-b-P4VP25) and poly(ethylene glycol)113-block-poly(4-hydroxy styrene)25 (PEG113-b-P4HS25) is shown to give rise to a cylindrical morphology in thin films through pyridine/phenol-based hetero-complementary hydrogen bonding interactions between the P4VP and P4HS copolymer segments. Removal of the cylindrical phase (PEG-b-P4HS) allowed access to porous materials having a pore surface decorated with P4VP polymer blocks. These segments could be transformed into cationic polyelectrolytes through quaternization of the pyridine nitrogen atom. The resulting positively charged nanopore surface could recognize negatively charged gold nanoparticles through electrostatic interactions. This work, therefore, outlines the utility of the supramolecular AB/CD type of block copolymer towards preparation of ordered porous thin films carrying a chemically defined channel surface with a large number of reactive sites.

Original languageEnglish
Pages (from-to)5755-5762
Number of pages8
JournalSoft Matter
Volume10
Issue number31
DOIs
Publication statusPublished - 2014 Aug 21

ASJC Scopus subject areas

  • Chemistry(all)
  • Condensed Matter Physics

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