Related Experiment Video
Updated: Apr 8, 2026

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
Published on: June 20, 2019
Arbitrary lattice symmetries via block copolymer nanomeshes
Pawel W Majewski1, Atikur Rahman1, Charles T Black1
1Center for Functional Nanomaterials, Brookhaven National Laboratory, Upton, New York 11973, USA.
Abstract:
Self-assembly of block copolymers is a powerful motif for spontaneously forming well-defined nanostructures over macroscopic areas. Yet, the inherent energy minimization criteria of self-assembly give rise to a limited library of structures; diblock copolymers naturally form spheres on a cubic lattice, hexagonally packed cylinders and alternating lamellae. Here, we demonstrate multicomponent nanomeshes with any desired lattice symmetry. We exploit photothermal annealing to rapidly order and align block copolymer phases over macroscopic areas, combined with conversion of the self-assembled organic phase into inorganic replicas. Repeated photothermal processing independently aligns successive layers, providing full control of the size, symmetry and composition of the nanoscale unit cell. We construct a variety of symmetries, most of which are not natively formed by block copolymers, including squares, rhombuses, rectangles and triangles. In fact, we demonstrate all possible two-dimensional Bravais lattices. Finally, we elucidate the influence of nanostructure on the electrical and optical properties of nanomeshes.
Related Concept Videos
Characteristics and Nomenclature of Copolymers
Lattice Centering and Coordination Number
Types of Unit Cells
Imagine taking a large number of identical...
The Seven Crystal Systems: Overview
Structures of Solids

