Creating surfactant nanoparticles for block copolymer composites through surface chemistry

Bumjoon J. Kim, Joona Bang, Craig J. Hawker, Julia J. Chiu, David J. Pine, Se Gyu Jang, Seung Man Yang, Edward J. Kramer

Research output: Contribution to journalArticle

Abstract

A simple strategy to tailor the surface of nanoparticles for their specific adsorption to and localization at block copolymer interfaces was explored. Gold nanoparticles coated by a mixture of low molecular weight thiol end-functional polystyrene (PS-SH) (M n = 1.5 and 3.4 kg/mol) and poly(2-vinylpyridine) homopolymers (P2VP-SH) (M n = 1.5 and 3.0 kg/mol) were incorporated into a lamellar poly(styrene-b-2-vinylpyridine) diblock copolymer (PS-b-P2VP) (M n = 196 kg/mol). A library of nanoparticles with varying PS and P2VP surface compositions (F PS) and high polymer ligand areal chain densities was synthesized. The location of the nanoparticles in the PS-b-P2VP block copolymer was determined by transmission electron microscopy. Sharp transitions in particle location from the PS domain to the PS/P2VP interface, and subsequently to the P2VP domain, were observed at F PS = 0.9 and 0.1, respectively. This extremely wide window of F PS values where the polymer-coated gold nanoparticles adsorb to the interface suggests a redistribution of PS and P2VP polymers on the Au surface, inducing the formation of amphiphilic nanoparticles at the PS/P2VP interface. In a second and synthetically more challenging approach, gold nanoparticles were covered with a thiol terminated random copolymer of styrene and 2-vinylpyridine synthesized by RAFT polymerization. Two different random copolymers were considered, where the molecular weight was fixed at 3.5 kg/mol and the relative incorporation of styrene and 2-vinylpyridine repeat units varied (F PS = 0.52 and 0.40). The areal chain density of these random copolymers on Au is unfortunately not high enough to preclude any contact between the P2VP block of the block copolymer and the Au surface. Interestingly, gold nanoparticles coated by the random copolymer with F PS = 0.4 were dispersed in the P2VP domain, while those with F PS = 0.52 were located at the interface. A simple calculation for the adsorption energy to the interface of the nanoparticles with different surface arrangements of PS and P2VP ligands supports evidence for the rearrangement of thiol terminated homopolymers. An upper limit estimate of the adsorption energy of nanoparticles uniformly coated with a random arrangement of PS and P2VP ligands where a 10% surface area was occupied by P2VP -mers or chains was ∼1 k BT, which indicates that such nanoparticles are unlikely to be segregated along the interface, in contrast to the experimental results for nanoparticles with mixed ligand-coated surfaces.

Original languageEnglish (US)
Pages (from-to)12693-12703
Number of pages11
JournalLangmuir
Volume23
Issue number25
DOIs
StatePublished - Dec 4 2007

ASJC Scopus subject areas

  • Materials Science(all)
  • Condensed Matter Physics
  • Surfaces and Interfaces
  • Spectroscopy
  • Electrochemistry

Fingerprint Dive into the research topics of 'Creating surfactant nanoparticles for block copolymer composites through surface chemistry'. Together they form a unique fingerprint.

  • Cite this

    Kim, B. J., Bang, J., Hawker, C. J., Chiu, J. J., Pine, D. J., Jang, S. G., Yang, S. M., & Kramer, E. J. (2007). Creating surfactant nanoparticles for block copolymer composites through surface chemistry. Langmuir, 23(25), 12693-12703. https://doi.org/10.1021/la701906n