Block copolymer (BCP) research has been developed extensively over the past few years due to its potential to form a variety of periodic structures via microphase separation. In addition, BCP films hold great potential for generating periodic nanostructures over large areas. Achieving well-ordered BCP nanopatterns is essential for understanding the self-assembly behavior of BCPs and the factors influencing these phenomena. Therefore, our group focuses on investigating the kinetics and phase separation behavior of block copolymer self-assembly in confined systems.
The following topics are of current interest to our group.
A. Fine-tuning of ordered structures of BCPs in thin films
B. Controlling disorder in BCP thin films
C. Interfacial self-assembly of BCPs at the air–water interface
In the self-assembly of sphere-forming block copolymers, the optimal packing structure is determined by a balance between entropic and enthalpic contributions. These contributions can be modulated by controlling external environments such as temperature and solvent quality. We investigate process-condition-dependent structural transformations of BCPs in thin films.
Representative paper
Direct Approach to High-Resolution, Square-Lattice Alternating Nanodot Array by Breaking Hexagonal Symmetry of Block Copolymer Spheres (Sci. Adv., 2025)
A Single Crystal 2D Hexagonal Array in a Centimeter Scale with a Self-Directed Assembly of Diblock Copolymer Spheres (ACS Nano, 2022)
Shear-Solvo Defect Annihilation of Diblock Copolymer Thin Films over a Large Area (Sci. Adv., 2019)
Disordered structures at the nanoscale have received increasing interest owing to their unique capability to localize wave-like quasiparticles - a renowned phenomenon known as Anderson localization. We present a methodology to construct such disordered structures by deliberately introducing a controlled degree of defects into hexagonal arrays of sphere- and cylinder-forming BCPs. By tuning various parameters such as metal precursor concentration and temperature, the spectrum of disorder is broadened. Our research potentially offers a platform for designing and engineering disordered systems that could mediate quasiparticle localization.
Amphiphilic block copolymers (BCPs) can form two-dimensionally confined structures through self-assembly at the air–water interface. These interfacial self-assembled BCP nanostructures can be used directly or applied to control interfacial energy. In both cases, we conduct systematic experiments by controlling various experimental parameters and investigate how these parameters affect the nanostructures of BCPs. Our research provides a new strategy for fabricating uniform arrays of diverse BCP nanopatterns and exploring their further applications.
Representative paper