Abstract

We report the lateral order and self-organized morphology of diblock copolymer polystyrene-block-poly(2-vinylpyridine), P(S-b-2VP), and micelles on silicon substrates (SiOx/Si). These micellar films were prepared by spin coating from polymer solutions of varied concentration of polymer in toluene onto SiOx/Si, and were investigated with grazing-incidence small-angle X-ray scattering (GISAXS) and an atomic force microscope (AFM). With progressively increased surface coverage with increasing concentration, loosely packed spherical micelles, ribbon-like nanostructures, and a second layer of spherical micelles were obtained sequentially. Quantitative analysis and simulations of the micellar packing demonstrates that the spatial ordering of the loosely packed spherical micelles altered from short-range order to hexagonal order when the micellar coverage increased from small to moderate densities of the covered surface. At large densities, anisotropic fusion between spherical micelles caused the ribbon-like nanostructures to have a short-range spatial order; the ordering quality of the second layer was governed by the rugged surface of the underlying layer because the valleys between the ribbon-like nanostructures allowed for further deposition of spherical micelles.

Highlights

  • Block copolymers (BCP) can self-assemble into ordered nanodomains with dimensional tunability and morphological diversity through control of such molecular parameters as the block volume fraction, molecular weight, chemical architecture, and segregation strength [1,2,3,4,5,6]

  • In contrast to that system [40], the micelles spun from toluene solutions reveal remarkably different packing and morphology of micelles on SiOx /Si, as reported by Li et al, but little interpretation was addressed to the packing and self-assembly of micelles that were spun from toluene [26]

  • Our intention here is to present a complete investigation of the packing and surface morphology of micelles spun from toluene by means of an atomic force microscope (AFM) and grazing-incidence small-angle X-ray scattering (GISAXS)

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Summary

Introduction

Block copolymers (BCP) can self-assemble into ordered nanodomains with dimensional tunability and morphological diversity through control of such molecular parameters as the block volume fraction, molecular weight, chemical architecture, and segregation strength [1,2,3,4,5,6]. Variation of solution conditions, such as solvent quality and polymer concentration, can yield ordered nanostructures in a wide range of morphologies or hierarchical assemblies, which form via kinetic control or in an equilibrium state [7,8,9,10]. Ordered arrays of spherical micelles of controlled size and inter-micelle distance are achievable through the manipulation of molecular masses, block volume fractions, interactions between segment and segment, segment and solvent and segment and substrate, and polymer concentrations [26,27,28,29,30,31,32,33].

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