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dc.contributor.authorLin, Yu-Liangen_US
dc.contributor.authorCheng, Ming-Hsiangen_US
dc.contributor.authorChang, Chun-Weien_US
dc.contributor.authorChu, Chien-Weien_US
dc.contributor.authorLiu, Chih-Tingen_US
dc.contributor.authorChen, Jiun-Taien_US
dc.date.accessioned2019-12-13T01:12:18Z-
dc.date.available2019-12-13T01:12:18Z-
dc.date.issued2019-11-07en_US
dc.identifier.issn1744-683Xen_US
dc.identifier.urihttp://dx.doi.org/10.1039/c9sm01633cen_US
dc.identifier.urihttp://hdl.handle.net/11536/153167-
dc.description.abstractIn this work, we study the structure transformations of cylinder-forming polystyrene-block-polydimethylsiloxane (PS31k-b-PDMS14.5k) confined in cylindrical nanopores. PS-b-PDMS nanotubes, nanospheres, and curved nanodiscs are ingeniously prepared by a facile template wetting strategy using anodic aluminum oxide (AAO) templates. Quantitative analyses of the structure transformations from nanospheres to curved nanodiscs are also conducted, showing that the lengths of the curved nanodiscs can be controlled by adjusting the annealing temperature and time. Furthermore, the PDMS domains of the nanostructures can be selectively etched using HF solutions, generating porous PS nanostructures. This work not only offers versatile routes to prepare block copolymer nanostructures with controlled shapes but also provides a deeper understanding of the structure transformation of block copolymers in confined geometries.en_US
dc.language.isoen_USen_US
dc.titleCurved block copolymer nanodiscs: structure transformations in cylindrical nanopores using the nonsolvent-assisted template wetting methoden_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c9sm01633cen_US
dc.identifier.journalSOFT MATTERen_US
dc.citation.volume15en_US
dc.citation.issue41en_US
dc.citation.spage8201en_US
dc.citation.epage8209en_US
dc.contributor.department交大名義發表zh_TW
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentNational Chiao Tung Universityen_US
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000491944400002en_US
dc.citation.woscount0en_US
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