Saito Masayuki, Yamada Norifumi L, Ito Kohzo, Yokoyama Hideaki
Graduate School of Frontier Sciences, The University of Tokyo, 5-1-5 Kashiwano-ha, Kashiwa, Chiba 277-8561, Japan.
Neutron Science Laboratory, High Energy Accelerator Research Organization, Ibaraki 319-1106, Japan.
Langmuir. 2020 Jun 16;36(23):6465-6472. doi: 10.1021/acs.langmuir.0c00764. Epub 2020 Jun 5.
Herein, the interfacial energy of a reconstructive polymer surface formed by segregation is analyzed by measuring the change in the size of elastomer thin films floating on water. When a system in which amphiphilic diblock copolymers are mixed with the hydrophobic elastomer is in contact with water, surface reconstruction is triggered by the segregation of copolymers with a gain in the hydration energy of the hydrophilic blocks. The hydrophilic brush layer spontaneously formed at the elastomer-water interface is named the dynamic polymer brush. Although it is anticipated that the interfacial energy will significantly decrease in the dynamic polymer brush system, a direct measurement of the interfacial energy of the reconstructive interface is a challenge. We propose a novel method to measure the interfacial energy of a reconstructive polymer surface by measuring the deformation of elastomer thin films floating on water and apply it to the dynamic polymer brush system. The interfacial energy of the dynamic polymer brush formed by the segregation of amphiphilic diblock copolymers with longer hydrophilic chains drastically decreased to zero due to the high hydration energy of hydrophilic chains. Based on the neutron reflectometry results, the graft density and thickness of the dynamic polymer brush system floating on water were found to be lower than those of the system fixed onto solid substrates. This indicates that the floating system can respond to an external environment with a high degree of freedom (graft density, brush thickness, and interface area).
在此,通过测量漂浮在水面上的弹性体薄膜尺寸的变化,分析了由偏析形成的重构聚合物表面的界面能。当两亲性二嵌段共聚物与疏水性弹性体混合的体系与水接触时,共聚物的偏析引发表面重构,亲水性嵌段的水合能增加。在弹性体 - 水界面自发形成的亲水性刷层被称为动态聚合物刷。尽管预计在动态聚合物刷体系中界面能会显著降低,但直接测量重构界面的界面能是一项挑战。我们提出了一种通过测量漂浮在水面上的弹性体薄膜的变形来测量重构聚合物表面界面能的新方法,并将其应用于动态聚合物刷体系。由于亲水性链的高水合能,由具有较长亲水性链的两亲性二嵌段共聚物偏析形成的动态聚合物刷的界面能急剧降至零。基于中子反射测量结果,发现漂浮在水面上的动态聚合物刷体系的接枝密度和厚度低于固定在固体基质上的体系。这表明漂浮体系能够以高度的自由度(接枝密度、刷厚度和界面面积)响应外部环境。