Center for Functional Nanomaterials, Brookhaven National Laboratory , Upton, New York 11973, United States.
ACS Nano. 2014 Jan 28;8(1):243-9. doi: 10.1021/nn4060539. Epub 2013 Dec 23.
Nanostructured grating surfaces with groove widths less than 200 nm impose boundary conditions that frustrate the natural molecular orientational ordering within thin films of blended polymer semiconductor poly(3-hexlythiophene) and phenyl-C61-butyric acid methyl ester, as revealed by grazing incidence X-ray scattering measurements. Polymer interactions with the grating sidewall strongly inhibit the polymer lamellar alignment parallel to the substrate typically found in planar films, in favor of alignment perpendicular to this orientation, resulting in a preferred equilibrium molecular configuration difficult to achieve by other means. Grating surfaces reduce the relative population of the parallel orientation from 30% to less than 5% in a 400 nm thick film. Analysis of in-plane X-ray scattering with respect to grating orientation shows polymer backbones highly oriented to within 10 degrees of parallel to the groove direction.
具有小于 200nm 槽宽的纳米结构光栅表面施加了边界条件,这些条件阻碍了混合聚合物半导体聚(3-己基噻吩)和苯基-C61-丁酸甲酯薄膜中分子的自然取向有序,这一点可以通过掠入射 X 射线散射测量揭示。与光栅侧壁的聚合物相互作用强烈抑制了通常在平面薄膜中发现的与衬底平行的聚合物层状排列,有利于与该方向垂直的排列,导致一种优选的平衡分子构象,这很难通过其他手段来实现。在 400nm 厚的薄膜中,光栅表面将平行取向的相对比例从 30%降低到小于 5%。相对于光栅取向的面内 X 射线散射分析表明,聚合物主链在与槽方向平行的 10 度以内高度取向。