Abstract

We investigate the nanostructures and phase diagrams of ABC linear triblock copolymers confined in spherical cavities by using real-space self-consistent field theory. Various 3D morphologies, such as spherical concentric lamellae, dumbbell-like cylinder, and rotational structures, are identified in the phase diagrams, which are constructed on the basis of the diameters of spherical cavities and the interaction between the polymers and preferential surfaces. We designate specific monomer-monomer interactions and block compositions, with which the polymers spontaneously form a cylindrical morphology in bulk, and firstly study morphology transformation with a neutral surface when a confining radius progressively increases. We then focus on phase morphologies under the preferential surfaces and consolidate them into phase diagrams. The spherical radius and the degree of preferential interactions can obviously induce the formation of a cylindrical morphology. Theoretical results correspond to an amount of recent experimental observations to a high degree and contribute to synthesising functional materials.

Highlights

  • Block copolymers are extensively circulated for their ability to self-assemble and form ordered morphologies at a nanoscale, thereby providing a development platform for fabrication techniques of multifunctional materials

  • On the basis of this basis of this foundation structure, we explore the effects of a neutral spherical confinement on a 1D

  • Foundation structure, we explore the effects of a neutral spherical confinement on a 1D phase diagram phase diagram by gradually increasing the effective diameter deff from 2.60 Rg to 8.60 Rg

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Summary

Introduction

Block copolymers are extensively circulated for their ability to self-assemble and form ordered morphologies at a nanoscale, thereby providing a development platform for fabrication techniques of multifunctional materials. Various external techniques have been developed in theoretical and experimental studies because the physical morphologies and properties of polymer nanoparticles are subject to the internal controlling parameters of polymers and influenced by external fields and space conditions. Hybrid nanomaterials that incorporate inorganic nanoparticles into self-assembled block copolymers under spherical nanoparticle confinement may be used in electronic and optics devices, which can combine the inherent properties of the two units and generate desirable properties [7]. Our work aims to reveal the mechanisms of phase separation and recombination into various nanostructures at the level of molecules

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