{"title":"周期自洽场理论中的动态掩模和外场:以双陀螺薄膜为例","authors":"Benjamin R. Magruder, and , Kevin D. Dorfman*, ","doi":"10.1021/acs.macromol.5c01458","DOIUrl":null,"url":null,"abstract":"<p >Self-consistent field theory (SCFT) accurately models the equilibrium thermodynamics of polymeric systems, including those under geometric confinement. Confinement is typically imposed in SCFT using a mask that modifies the incompressibility constraint─an approach that is limited to systems with rigid boundaries. Here we derive a “dynamic mask method” that allows a nonrigid boundary to be modeled within standard periodic SCFT by optimizing the confining geometry during a single calculation. The method requires only that the confining geometry be defined in terms of the lattice parameters of the calculation box. A corresponding technique is also derived to optimize externally imposed chemical potential fields. The method is then used to model thin films of self-assembled diblock polymers in a high-throughput manner, where the film thickness can be relaxed within a single SCFT calculation to a commensurate value that minimizes the areal excess free energy. Specifically, we extend our previous work on thin films of the double-gyroid phase, revealing that changes in segregation strength χ<i>N</i> and conformational asymmetry <i>b</i><sub>A</sub>/<i>b</i><sub>B</sub> do not significantly affect the relative stability of different orientations of the double gyroid, meaning that the “boundary frustration” model developed previously is generalizable to any neat melt of AB diblock polymer.</p>","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"58 15","pages":"8555–8567"},"PeriodicalIF":5.2000,"publicationDate":"2025-07-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dynamic Masks and External Fields in Periodic Self-Consistent Field Theory: A Case Study on Double-Gyroid Thin Films\",\"authors\":\"Benjamin R. Magruder, and , Kevin D. Dorfman*, \",\"doi\":\"10.1021/acs.macromol.5c01458\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Self-consistent field theory (SCFT) accurately models the equilibrium thermodynamics of polymeric systems, including those under geometric confinement. Confinement is typically imposed in SCFT using a mask that modifies the incompressibility constraint─an approach that is limited to systems with rigid boundaries. Here we derive a “dynamic mask method” that allows a nonrigid boundary to be modeled within standard periodic SCFT by optimizing the confining geometry during a single calculation. The method requires only that the confining geometry be defined in terms of the lattice parameters of the calculation box. A corresponding technique is also derived to optimize externally imposed chemical potential fields. The method is then used to model thin films of self-assembled diblock polymers in a high-throughput manner, where the film thickness can be relaxed within a single SCFT calculation to a commensurate value that minimizes the areal excess free energy. Specifically, we extend our previous work on thin films of the double-gyroid phase, revealing that changes in segregation strength χ<i>N</i> and conformational asymmetry <i>b</i><sub>A</sub>/<i>b</i><sub>B</sub> do not significantly affect the relative stability of different orientations of the double gyroid, meaning that the “boundary frustration” model developed previously is generalizable to any neat melt of AB diblock polymer.</p>\",\"PeriodicalId\":51,\"journal\":{\"name\":\"Macromolecules\",\"volume\":\"58 15\",\"pages\":\"8555–8567\"},\"PeriodicalIF\":5.2000,\"publicationDate\":\"2025-07-16\",\"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.5c01458\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecules","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.macromol.5c01458","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Dynamic Masks and External Fields in Periodic Self-Consistent Field Theory: A Case Study on Double-Gyroid Thin Films
Self-consistent field theory (SCFT) accurately models the equilibrium thermodynamics of polymeric systems, including those under geometric confinement. Confinement is typically imposed in SCFT using a mask that modifies the incompressibility constraint─an approach that is limited to systems with rigid boundaries. Here we derive a “dynamic mask method” that allows a nonrigid boundary to be modeled within standard periodic SCFT by optimizing the confining geometry during a single calculation. The method requires only that the confining geometry be defined in terms of the lattice parameters of the calculation box. A corresponding technique is also derived to optimize externally imposed chemical potential fields. The method is then used to model thin films of self-assembled diblock polymers in a high-throughput manner, where the film thickness can be relaxed within a single SCFT calculation to a commensurate value that minimizes the areal excess free energy. Specifically, we extend our previous work on thin films of the double-gyroid phase, revealing that changes in segregation strength χN and conformational asymmetry bA/bB do not significantly affect the relative stability of different orientations of the double gyroid, meaning that the “boundary frustration” model developed previously is generalizable to any neat melt of AB diblock polymer.
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.