Issue 40, 2024

Constructing phase diagrams of block copolymers with A-block-(B-stat-C) architecture

Abstract

Block copolymers (BCPs) are capable of self-organizing into precise nanoscale structures, generating interest across diverse fields such as drug delivery, catalysis, and lithography. Introducing new functionalities to BCPs through post-modification is a widely used approach. To further advance the design of functional BCPs, it is essential to understand how the incorporated functional groups affect their morphology. In this study, we focus on BCPs with an A-block-(B-statistical-C) architecture, where A is poly(styrene), B is poly(methyl methacrylate), and C is poly(2-hydroxyethyl methacrylate), which allows for the addition of photo-crosslinkable groups like methacrylates. In particular, we have synthesized a library of over twenty well-defined BCPs with different compositions and molecular weights using RAFT polymerization. Afterwards, we created a second library by introducing methacrylate groups through post-functionalization. The morphologies of these two sets of BCPs were carefully analyzed using small-angle X-ray scattering (SAXS), scanning electron microscopy (SEM), and infrared scanning near-field optical microscopy (IR-SNOM). By combining this data, we have built phase diagrams for both the original and functionalized copolymers and examined how post-functionalization affects their morphology. Our findings reveal that even small changes in the polymer composition significantly impact the morphological behavior.

Graphical abstract: Constructing phase diagrams of block copolymers with A-block-(B-stat-C) architecture

Supplementary files

Article information

Article type
Paper
Submitted
07 Aug 2024
Accepted
17 Sep 2024
First published
20 Sep 2024
This article is Open Access
Creative Commons BY license

Polym. Chem., 2024,15, 4093-4100

Constructing phase diagrams of block copolymers with A-block-(B-stat-C) architecture

B. Weidinger, N. von Coelln, G. Yang, H. Nirschl, I. Wacker, R. R. Schröder, P. Tegeder and E. Blasco, Polym. Chem., 2024, 15, 4093 DOI: 10.1039/D4PY00872C

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