Majewski Pawel W, Rahman Atikur, Black Charles T, Yager Kevin G
Center for Functional Nanomaterials, Brookhaven National Laboratory, Upton, New York 11973, USA.
Nat Commun. 2015 Jun 23;6:7448. doi: 10.1038/ncomms8448.
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.
嵌段共聚物的自组装是一种强大的模式,可在宏观区域自发形成定义明确的纳米结构。然而,自组装固有的能量最小化标准导致结构库有限;二嵌段共聚物自然会在立方晶格上形成球体、六方密堆积圆柱体和交替的片层。在这里,我们展示了具有任何所需晶格对称性的多组分纳米网格。我们利用光热退火在宏观区域快速排列和对齐嵌段共聚物相,并将自组装的有机相转化为无机复制品。重复的光热加工独立地对齐连续的层,从而全面控制纳米级晶胞的尺寸、对称性和组成。我们构建了多种对称性结构,其中大多数并非嵌段共聚物天然形成的,包括正方形、菱形、矩形和三角形。事实上,我们展示了所有可能的二维布拉维晶格。最后,我们阐明了纳米结构对纳米网格电学和光学性质的影响。