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dc.contributor.authorInoue, R.en
dc.contributor.authorKanaya, Toshijien
dc.contributor.authorNishida, K.en
dc.contributor.authorTsukushi, I.en
dc.contributor.authorTelling, M. T. F.en
dc.contributor.authorGabrys, B. J.en
dc.contributor.authorTyagi, M.en
dc.contributor.authorSoles, C.en
dc.contributor.authorWu, W.-l.en
dc.contributor.alternative金谷, 利治ja
dc.date.accessioned2009-11-16T05:49:24Z-
dc.date.available2009-11-16T05:49:24Z-
dc.date.issued2009-09-
dc.identifier.issn1539-3755-
dc.identifier.urihttp://hdl.handle.net/2433/87317-
dc.description.abstractExtensive studies on polymer thin films to date have revealed their interesting but unusual properties such as film thickness dependence of glass transition temperature Tg and thermal expansivity. Recent studies have shown that the lower Tg is not always related to the higher mobility in polymer thin films, which contradicts our current understanding of the glass transition process. In this work, we report the results of inelastic neutron-scattering measurements on polystyrene thin films using two spectrometers with different energy resolutions as well as ellipsometry measurements. The results are interpreted in terms of cooperatively rearranging region and motional slowing down due to the surface effect that explain plausibly the anomalous relationship between the glass transition temperature Tg and the molecular mobility in thin films.en
dc.language.isoeng-
dc.publisherAmerican Physical Societyen
dc.rightsc 2009 The American Physical Society.en
dc.titleGlass transition and molecular mobility in polymer thin filmsen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitlePhysical Review E - Statistical, Nonlinear, and Soft Matter Physicsen
dc.identifier.volume80-
dc.identifier.issue3-
dc.relation.doi10.1103/PhysRevE.80.031802-
dc.textversionpublisher-
dc.identifier.artnum031802-
dc.identifier.pmid19905138-
dcterms.accessRightsopen access-
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