4.7 Article

Functional nanoparticle-driven self-assembled diblock copolymer hybrid nano-patterns

Journal

POLYMER CHEMISTRY
Volume 13, Issue 13, Pages 1920-1930

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2py00121g

Keywords

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Funding

  1. Doctoral School (ED211) of E2S UPPA

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In this study, we demonstrate how functional gold nanoparticles can manipulate the morphology of block copolymer thin films. By employing post-polymerization modifications, we synthesized a unique block copolymer with special structure and investigated its self-assembly behavior. Additionally, the impact of incorporating polystyrene-capped gold nanoparticles on the morphology of the block copolymer thin film was analyzed.
Herein, we report how functional gold nanoparticles can drive the block copolymer BCP thin film morphologies of polystyrene-block-poly(vinylbenzyl-3-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)prop-1-yne (PS-b-PVBEG). PS-b-PVBEG was obtained via Nitroxide Mediated Polymerization and two consecutive post-polymerization modifications, a nucleophilic substitution (S(N)2) between polystyrene-b-poly(vinylbenzyl chloride) (PS-b-PVBC) and NaN3, and a Huisgen cycloaddition with mPEG3-propargyl. The self-assembly in bulk of the intermediate block copolymers PS-b-PVBC and PS-b-PVBN3 and the final PS-b-PVBEG one were studied as well as the change of the morphology of PS-b-PVBEG with the incorporation of polystyrene-capped gold nanoparticles (GNPs@PS). The morphology of the hybrid films was characterized by Atomic Force Microscopy (AFM) and the correlation between the morphology and the chemical composition of the surface is finely investigated by X-ray Photo-electron Spectroscopy (XPS). A high correlation is observed between the chemical composition of the surface of the hybrid film and its morphology transition from PS lamellae to out-of-plane PVBEG cylinders by GNPs@PS addition.

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