{"title":"Mechanisms of Multiple Reentrant Transitions between Frank-Kasper and Classical Spherical Phases in AB-Type Dendron-Like Copolymer","authors":"Hongyan Chen, , , Qingshu Dong, , , Yicheng Qiang*, , , Li Peng, , , Xianbo Huang*, , and , Weihua Li*, ","doi":"10.1021/acs.macromol.5c02113","DOIUrl":null,"url":null,"abstract":"<p >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 (<i>f</i>). Qiang et al. drastically expand the spherical region to <i>f</i> > 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 <i>f</i> 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.</p>","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"58 18","pages":"10192–10202"},"PeriodicalIF":5.2000,"publicationDate":"2025-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecules","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.macromol.5c02113","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
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.
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.