{"title":"圆柱约束下层次结构的产生与稳定性","authors":"Tiancheng Chen, Yuci Xu","doi":"10.1002/mats.202200076","DOIUrl":null,"url":null,"abstract":"<p>Focusing on the formation of hierarchical structure under cylindrical confinement, the self-assembly of A(BC)<sub>2</sub>B multiblock copolymer of chain length <i>N</i> in a nanopore with size <i>R</i> is studied using the self-consistent field theory. The hierarchical concentric ring (HC<sub><i>k</i></sub>), hierarchical perforated cylinder (HP<sub><i>k</i></sub>), hierarchical helix (HH<sub><i>k</i></sub>), and even hierarchical disk (HD<sub><i>k</i></sub>) is obtained with different number of mid-thin layers <i>k</i> via a proposed design principle. The results show that large pore size and <i>χ</i><sub>AB</sub> favor the hierarchical structure with more <i>k</i>, while <i>χ</i><sub><i>BC</i></sub> prefers hierarchical structure with less <i>k</i>, consistent with the results of hierarchical structure in bulk. By investigating the effect of the volume fraction of the tail A block (<i>f</i><sub>A</sub>), the phase transition sequence, HC<sub><i>k</i></sub> → HP<sub><i>k</i></sub> → HH<sub><i>k</i></sub> → HD<sub><i>k</i></sub> is explored, which shares the same transition of multiblock copolymer in bulk with L<sub><i>k</i></sub> → G<sub><i>k</i></sub> → C<sub><i>k</i></sub> → S<sub><i>k</i></sub>. Finally, the phase diagram with respect to the <i>f</i><sub>A</sub> and <i>R</i> is explored, where the stability regime of these hierarchical structures is well understood. The results provide a compelling panacea for the fabrication of hierarchical 3D nanostructures under confinement.</p>","PeriodicalId":18157,"journal":{"name":"Macromolecular Theory and Simulations","volume":"32 3","pages":""},"PeriodicalIF":1.8000,"publicationDate":"2023-02-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Emergence and Stability of Hierarchical Structures under Cylindrical Confinement\",\"authors\":\"Tiancheng Chen, Yuci Xu\",\"doi\":\"10.1002/mats.202200076\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Focusing on the formation of hierarchical structure under cylindrical confinement, the self-assembly of A(BC)<sub>2</sub>B multiblock copolymer of chain length <i>N</i> in a nanopore with size <i>R</i> is studied using the self-consistent field theory. The hierarchical concentric ring (HC<sub><i>k</i></sub>), hierarchical perforated cylinder (HP<sub><i>k</i></sub>), hierarchical helix (HH<sub><i>k</i></sub>), and even hierarchical disk (HD<sub><i>k</i></sub>) is obtained with different number of mid-thin layers <i>k</i> via a proposed design principle. The results show that large pore size and <i>χ</i><sub>AB</sub> favor the hierarchical structure with more <i>k</i>, while <i>χ</i><sub><i>BC</i></sub> prefers hierarchical structure with less <i>k</i>, consistent with the results of hierarchical structure in bulk. By investigating the effect of the volume fraction of the tail A block (<i>f</i><sub>A</sub>), the phase transition sequence, HC<sub><i>k</i></sub> → HP<sub><i>k</i></sub> → HH<sub><i>k</i></sub> → HD<sub><i>k</i></sub> is explored, which shares the same transition of multiblock copolymer in bulk with L<sub><i>k</i></sub> → G<sub><i>k</i></sub> → C<sub><i>k</i></sub> → S<sub><i>k</i></sub>. Finally, the phase diagram with respect to the <i>f</i><sub>A</sub> and <i>R</i> is explored, where the stability regime of these hierarchical structures is well understood. The results provide a compelling panacea for the fabrication of hierarchical 3D nanostructures under confinement.</p>\",\"PeriodicalId\":18157,\"journal\":{\"name\":\"Macromolecular Theory and Simulations\",\"volume\":\"32 3\",\"pages\":\"\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2023-02-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Macromolecular Theory and Simulations\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/mats.202200076\",\"RegionNum\":4,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecular Theory and Simulations","FirstCategoryId":"5","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/mats.202200076","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Emergence and Stability of Hierarchical Structures under Cylindrical Confinement
Focusing on the formation of hierarchical structure under cylindrical confinement, the self-assembly of A(BC)2B multiblock copolymer of chain length N in a nanopore with size R is studied using the self-consistent field theory. The hierarchical concentric ring (HCk), hierarchical perforated cylinder (HPk), hierarchical helix (HHk), and even hierarchical disk (HDk) is obtained with different number of mid-thin layers k via a proposed design principle. The results show that large pore size and χAB favor the hierarchical structure with more k, while χBC prefers hierarchical structure with less k, consistent with the results of hierarchical structure in bulk. By investigating the effect of the volume fraction of the tail A block (fA), the phase transition sequence, HCk → HPk → HHk → HDk is explored, which shares the same transition of multiblock copolymer in bulk with Lk → Gk → Ck → Sk. Finally, the phase diagram with respect to the fA and R is explored, where the stability regime of these hierarchical structures is well understood. The results provide a compelling panacea for the fabrication of hierarchical 3D nanostructures under confinement.
期刊介绍:
Macromolecular Theory and Simulations is the only high-quality polymer science journal dedicated exclusively to theory and simulations, covering all aspects from macromolecular theory to advanced computer simulation techniques.