Abstract

Electron microscopy has proved to be a major tool to study the structure of self-assembled amphiphilic block copolymer particles. These specimens, like supramolecular biological structures, are problematic for electron microscopy because of their poor capacity to scatter electrons and their susceptibility to radiation damage and dehydration. Sub-50 nm core-shell spherical particles made up of poly(hydroxyethyl acrylate)–b–poly(styrene) are prepared via polymerization-induced self-assembly (PISA). For their morphological characterization, we discuss the advantages, limitations, and artefacts of TEM with or without staining, cryo-TEM, and SEM. A number of technical points are addressed such as precisely shaping of particle boundaries, resolving the particle shell, differentiating particle core and shell, and the effect of sample drying and staining. TEM without staining and cryo-TEM largely evaluate the core diameter. Negative staining TEM is more efficient than positive staining TEM to preserve native structure and to visualize the entire particle volume. However, no technique allows for a satisfactory imaging of both core and shell regions. The presence of long protruding chains is manifested by patched structure in cryo-TEM and a significant edge effect in SEM. This manuscript provides a basis for polymer chemists to develop their own specimen preparations and to tackle the interpretation of challenging systems.

Highlights

  • One major interest of amphiphilic block copolymers lies in their ability to form aggregates of high morphological complexity

  • We reported the morphological characterization of two PHEAx –b–PS130 copolymer nanoparticles bearing short and long PHEA stabilizing blocks (x = 23 and 85) using TEM, cryo-TEM, and SEM

  • PHEA23 –b–PS130 was too short to be resolved, regardless of the method. This explains why the particle size given by the three electron microscopy (EM) techniques were in the same average order

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Summary

Introduction

One major interest of amphiphilic block copolymers lies in their ability to form aggregates of high morphological complexity. There is an abundance of studies using amphiphilic block copolymers of different compositions and block lengths that are able to self-assemble into a variety of supramolecular aggregates, such as spheres, rods, lamellae, and vesicles [1]. It should be noted that not all these block copolymer supramolecular structures can be deemed nano-objects (or nanoparticles)—only those whose three dimensions span from approximately 1 to 100 nm can be [2]. Spherical nanoparticles are the most common and investigated copolymer nano-objects [3]. Among the plethora of methods developed for the formation of spherical, amphiphilic block copolymer nanoparticles, nanoprecipitation and polymerization-induced self-assembly (PISA) are the most popular

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