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dc.contributor.authorLee, Yeonhee-
dc.contributor.authorLee, Jihye-
dc.contributor.authorLim, Weon Cheol-
dc.contributor.authorShin, Kwanwoo-
dc.contributor.authorKim, Kang-Jin-
dc.date.accessioned2024-01-20T18:00:49Z-
dc.date.available2024-01-20T18:00:49Z-
dc.date.created2021-09-05-
dc.date.issued2011-01-
dc.identifier.issn0142-2421-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/130750-
dc.description.abstractThe morphology from symmetric diblock copolymers of poly(styrene-b-propylmethacrylate) (PS-PPrMA), where polystyrene (PS) block was perdeuterated near the copolymer/air and copolymer/substrate interfaces and in the bulk, was characterized by using time-of-flight secondary ion mass spectrometry (TOF-SIMS). Elemental depth profiles measured in the negative ion mode by a Cs+ primary ion beam demonstrate variations in hydrogen, deuterium, carbon, oxygen and hydrocarbons within the diblock copolymer according to the depth. The annealed deuterated poly(styrene-b-propylmethacrylate) (dPS-PPrMA) copolymer samples showed a decrease in the deuterated PS secondary ion peak intensity as compared to the as-cast samples. TOF-SIMS depth profiling was obtained for the lamellar morphology of dPS-PPrMA which is found to orient parallel to the surface of the substrate. This preferential orientation resulted in a periodic variation in the composition of each block that continued through the entire copolymer film with thickness of 700 and 2100 angstrom. Temperature-dependent annealing studies on dPS-PPrMA thin film on the silicon substrates were performed to investigate the lower critical ordering transition (LCOT) properties of diblock copolymers. Copyright (C) 2010 John Wiley & Sons, Ltd.-
dc.languageEnglish-
dc.publisherWILEY-BLACKWELL-
dc.subjectION MASS-SPECTROMETRY-
dc.subjectPOLYMER THIN-FILMS-
dc.subjectBLOCK-COPOLYMERS-
dc.subjectX-RAY-
dc.subjectSURFACE-
dc.subjectAFM-
dc.subjectORIENTATION-
dc.subjectMORPHOLOGY-
dc.subjectSUBSTRATE-
dc.subjectBEHAVIOR-
dc.titleDepth profiling of lamella-phase diblock copolymers using SIMS-
dc.typeArticle-
dc.identifier.doi10.1002/sia.3511-
dc.description.journalClass1-
dc.identifier.bibliographicCitationSURFACE AND INTERFACE ANALYSIS, v.43, no.1-2, pp.277 - 280-
dc.citation.titleSURFACE AND INTERFACE ANALYSIS-
dc.citation.volume43-
dc.citation.number1-2-
dc.citation.startPage277-
dc.citation.endPage280-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000287669500070-
dc.identifier.scopusid2-s2.0-78951475282-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle; Proceedings Paper-
dc.subject.keywordPlusION MASS-SPECTROMETRY-
dc.subject.keywordPlusPOLYMER THIN-FILMS-
dc.subject.keywordPlusBLOCK-COPOLYMERS-
dc.subject.keywordPlusX-RAY-
dc.subject.keywordPlusSURFACE-
dc.subject.keywordPlusAFM-
dc.subject.keywordPlusORIENTATION-
dc.subject.keywordPlusMORPHOLOGY-
dc.subject.keywordPlusSUBSTRATE-
dc.subject.keywordPlusBEHAVIOR-
dc.subject.keywordAuthordepth profiling-
dc.subject.keywordAuthordiblock copolymer-
dc.subject.keywordAuthorphase separation-
dc.subject.keywordAuthorTOF-SIMS-
dc.subject.keywordAuthorPS-
dc.subject.keywordAuthorPPrMA-
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