Nielsen Bjarke Frost, Linga Gaute, Christensen Amalie, Mathiesen Joachim
Niels Bohr Institute, University of Copenhagen, 2100 Copenhagen, Denmark.
PoreLab, The Njord Centre, Department of Physics, University of Oslo, P. O. Box 1048, 0316 Oslo, Norway.
Soft Matter. 2020 Apr 8;16(14):3395-3406. doi: 10.1039/c9sm02389e.
Self-assembly of ordered nanometer-scale patterns is interesting in itself, but its practical value depends on the ability to predict and control pattern formation. In this paper we demonstrate theoretically and numerically that engineering of extrinsic as well as intrinsic substrate geometry may provide such a controllable ordering mechanism for block copolymers films. We develop an effective two-dimensional model of thin films of striped-phase diblock copolymers on general curved substrates. The model is obtained as an expansion in the film thickness and thus takes the third dimension into account, which crucially allows us to predict the preferred orientations even in the absence of intrinsic curvature. We determine the minimum-energy textures on several curved surfaces and arrive at a general principle for using substrate curvature as an ordering field, namely that the stripes will tend to align along directions of maximal curvature.
有序纳米尺度图案的自组装本身就很有趣,但其实际价值取决于预测和控制图案形成的能力。在本文中,我们通过理论和数值证明,外在以及内在衬底几何结构的工程设计可为嵌段共聚物薄膜提供这样一种可控的有序机制。我们针对一般弯曲衬底上的条纹相双嵌段共聚物薄膜开发了一个有效的二维模型。该模型是通过薄膜厚度的展开得到的,因此考虑了第三维,这至关重要地使我们即使在没有内在曲率的情况下也能预测优选取向。我们确定了几个曲面上的最低能量织构,并得出了将衬底曲率用作有序场的一般原则,即条纹将倾向于沿最大曲率方向排列。