Mechanisms of Multiple Reentrant Transitions between Frank-Kasper and Classical Spherical Phases in AB-Type Dendron-Like Copolymer

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Hongyan Chen, , , Qingshu Dong, , , Yicheng Qiang*, , , Li Peng, , , Xianbo Huang*, , and , Weihua Li*, 
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Abstract

It has been commonly accepted that Frank-Kasper spherical phases are stabilized over the classical phases in AB-type block copolymers by expanding the spherical region toward a large volume fraction of the A-block (f). Qiang et al. drastically expand the spherical region to f > 0.5 and find multiple reentrant transitions between Frank-Kasper and classical phases, the mechanisms of which have not yet been fully understood. In this work, we probe into the mechanisms by quantitatively analyzing the geometrical deformation of domains as well as its relationship with the chain architecture. As f increases, domains undergo convex deformation, followed by concave deformation to release the nonuniformity of stretching of short B-blocks filling the matrix. When convex deformation solely occurs, Frank-Kasper phases are favorable due to their milder deformation. As concave deformation starts to appear, the classical phases become more stable because their more convex deformation at the vertices of the Voronoi cell can alleviate the concave deformation on the faces. Moreover, it is revealed that the geometrical deformation is closely related with the dendritic architecture.

Abstract Image

Abstract Image

ab型枝状共聚物中Frank-Kasper相与经典球形相多重可重入跃迁机理
人们普遍认为,在ab型嵌段共聚物中,Frank-Kasper球形相通过向a嵌段的较大体积分数(f)扩展球形区域而比经典相稳定。Qiang等人将球面区域大幅扩展到f >; 0.5,并发现了Frank-Kasper相与经典相之间的多次可重入跃迁,其机制尚未完全了解。在这项工作中,我们通过定量分析域的几何变形及其与链结构的关系来探讨其机制。随着f的增大,区域先发生凸变形,再发生凹变形,以解除填充矩阵的短b块拉伸的不均匀性。当仅发生凸变形时,Frank-Kasper相由于其较温和的变形而有利。当凹变形开始出现时,经典相变得更加稳定,因为它们在Voronoi细胞顶点处的凸变形可以缓解面上的凹变形。此外,几何变形与枝晶结构密切相关。
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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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