Otsuka Issei, Isono Takuya, Rochas Cyrille, Halila Sami, Fort Sébastien, Satoh Toshifumi, Kakuchi Toyoji, Borsali Redouane
Centre de Recherches sur les Macromolécules Végétales (CERMAV, UPR-CNRS 5301), affiliated with the Université Joseph Fourier (UJF) and member of the Institut de Chimie Moléculaire de Grenoble (ICMG, FR-CNRS 2607), BP53, 38041 Grenoble Cedex 9, France.
Graduate School of Chemical Sciences and Engineering and Faculty of Engineering, Hokkaido University, Sapporo 060-8628, Japan.
ACS Macro Lett. 2012 Dec 18;1(12):1379-1382. doi: 10.1021/mz300543u. Epub 2012 Nov 19.
To date, the feature size of microphase separation in block copolymers has been downsizing to 10 nm scale. However, morphological control for such a small feature is still a challenging task. The present Letter discusses a phase transition in a natural/synthetic "hybrid" block copolymer system based on an oligosaccharide and poly(ε-caprolactone) via thermal annealing. Time-resolved small-angle X-ray scattering investigation as a function of temperature indicated the phase transition from hexagonally close-packed cylinder to body-centered cubic at 10 nm scale. Atomic force microscope images of the block copolymer thin films annealed at different temperatures clearly confirmed the existence of these morphologies. The driving force of this phase transition (from cylinder to cubic) is the change of volume fraction of the block copolymer due to thermal caramelization.
迄今为止,嵌段共聚物中微相分离的特征尺寸已缩小至10纳米尺度。然而,对如此小的特征进行形态控制仍是一项具有挑战性的任务。本信函讨论了基于低聚糖和聚(ε-己内酯)的天然/合成“杂化”嵌段共聚物体系通过热退火发生的相变。作为温度函数的时间分辨小角X射线散射研究表明,在10纳米尺度上发生了从六方密排圆柱到体心立方的相变。在不同温度下退火的嵌段共聚物薄膜的原子力显微镜图像清楚地证实了这些形态的存在。这种相变(从圆柱到立方)的驱动力是由于热焦糖化导致的嵌段共聚物体积分数的变化。