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Heat-induced spontaneous and damage-free separation of transparent polymer thin films based on clickable decomposition of pyrolytic core-shell nanocapsules

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dc.contributor.authorAn, Jongil-
dc.contributor.authorKim, Soyern-
dc.contributor.authorChoi, Jin-Wook-
dc.contributor.authorSon, Seung-Rak-
dc.contributor.authorPark, Jisung-
dc.contributor.authorPark, Chan Beom-
dc.contributor.authorLee, Jun Hyup-
dc.date.accessioned2022-03-11T05:40:06Z-
dc.date.available2022-03-11T05:40:06Z-
dc.date.created2022-03-11-
dc.date.issued2022-03-
dc.identifier.issn2352-4928-
dc.identifier.urihttp://scholarworks.bwise.kr/ssu/handle/2018.sw.ssu/42002-
dc.description.abstractThe automatic and damage-free manipulation for efficient separation of polymer thin films from various substrates has received growing interests in a broad range of applications from electronic devices to optical films because it can realize the innovative recycling and on-demand spontaneous detachment of scarce and valuable materials. Herein, we demonstrate a spontaneous and damage-free separation methodology for transparent polymer thin films based on the heat-induced microbubble generation from pyrolytic core-shell nanocapsules at the interface between the substrate and the thin film. The pyrolytic polymer nanocapsules were fabricated by encapsulating a latent gas-forming agent of benzenesulfonyl hydrazine in the crosslinked copolymer nanoparticle comprising polyacrylonitrile and poly(methyl methacrylate). The heat-induced clickable decomposition of pyrolytic core-shell nanocapsules generated a significant number of microbubbles inside the thin film, thereby inducing instantaneous and effortless detachment of the transparent film from substrate. The fabricated polymer thin films embedded with a small number of pyrolytic polymer nanocapsules afforded an excellent debonding performance with a maximum efficiency of 93.4% after short thermal treatment compared to that of the pristine thin films, simultaneously maintaining a remarkable optical clarity of about 99% and a high initial adhesion strength with a maximum of approximately 22 kgf cm(-2).-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER-
dc.relation.isPartOfMATERIALS TODAY COMMUNICATIONS-
dc.titleHeat-induced spontaneous and damage-free separation of transparent polymer thin films based on clickable decomposition of pyrolytic core-shell nanocapsules-
dc.typeArticle-
dc.identifier.doi10.1016/j.mtcomm.2021.103079-
dc.type.rimsART-
dc.identifier.bibliographicCitationMATERIALS TODAY COMMUNICATIONS, v.30-
dc.description.journalClass1-
dc.identifier.wosid000736583100001-
dc.identifier.scopusid2-s2.0-85121223170-
dc.citation.titleMATERIALS TODAY COMMUNICATIONS-
dc.citation.volume30-
dc.contributor.affiliatedAuthorLee, Jun Hyup-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.subject.keywordAuthorMicrobubbles-
dc.subject.keywordAuthorPolymer thin films-
dc.subject.keywordAuthorPyrolytic nanocapsules-
dc.subject.keywordAuthorSpontaneous separation-
dc.subject.keywordAuthorThermal decomposition-
dc.subject.keywordPlusTHERMALLY-EXPANDABLE MICROSPHERES-
dc.subject.keywordPlusSUSPENSION POLYMERIZATION-
dc.subject.keywordPlusADHESIVES-
dc.subject.keywordPlusBEHAVIOR-
dc.subject.keywordPlusSTRENGTH-
dc.subject.keywordPlusPMMA-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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