共聚物
块(置换群论)
聚合物
材料科学
化学物理
形态学(生物学)
自组装
光学(聚焦)
明星(博弈论)
超分子化学
高分子化学
纳米技术
化学
结晶学
物理
复合材料
数学
组合数学
光学
地质学
天体物理学
古生物学
晶体结构
作者
Yushu Matsushita,Atsushi Takano,Marylène Vayer,Christophe Sinturel
标识
DOI:10.1002/admi.201902007
摘要
Abstract During the self‐assembly process of block copolymers, interfaces are formed as a result of the microphase separation between the blocks. The location of the polymer chains and block junctions with respect to these interfaces is crucial and drives the morphology. It depends on the dispersities (e.g., molecular mass and composition) of the blocks, their architectures (e.g., linear vs star), and the type of interaction (e.g., repulsion vs attraction). In this review, the authors focus on the formation of unusual morphologies that are obtained in the following three categories: i) multimodal blends of block polymers, ii) star block polymers, and iii) supramolecular assemblies composed of block copolymers. Although these three examples seem to be very different from one another, the authors demonstrate in this review that they all share a constrained location of their chains and/or junctions with respect to the interfaces. In this sense, they deviate from the common behavior of simple linear block copolymers, in which the junctions are located on the interface and homogeneously distributed onto it.
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