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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/35297
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dc.contributor.authorCastro, Fernando A.-
dc.contributor.authorGraeff, Carlos Frederico de Oliveira-
dc.contributor.authorHeier, Jakob-
dc.contributor.authorHany, Roland-
dc.date.accessioned2014-05-20T15:24:45Z-
dc.date.accessioned2016-10-25T17:59:03Z-
dc.date.available2014-05-20T15:24:45Z-
dc.date.available2016-10-25T17:59:03Z-
dc.date.issued2007-04-05-
dc.identifierhttp://dx.doi.org/10.1016/j.polymer.2007.02.059-
dc.identifier.citationPolymer. Oxford: Elsevier B.V., v. 48, n. 8, p. 2380-2386, 2007.-
dc.identifier.issn0032-3861-
dc.identifier.urihttp://hdl.handle.net/11449/35297-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/35297-
dc.description.abstractWe present atomic force microscopic images of the interphase morphology of vertically segregated thin films spin coated from two-component mixtures of poly[2-methoxy-5-(2'-ethylhexyloxy)-1,4-phenylene-vinylene] (MEH-PPV) and polystyrene (PS). We investigate the mechanism leading to the formation of wetting layers and lateral structures during spin coating using different PS molecular weights, solvents and blend compositions. Spinodal decomposition competes with the formation of surface enrichment layers. The spinodal wavelength as a function of PS molecular weight follows a power-law similar to bulk-like spinodal decomposition. Our experimental results indicate that length scales of interface topographical features can be adjusted from the nanometer to micrometer range. The importance of controlled arrangement of semiconducting polymers in thin film geometries for organic optoelectronic device applications is discussed. (c) 2007 Elsevier Ltd. All rights reserved.en
dc.format.extent2380-2386-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectpolymer demixingpt
dc.subjectpolymer blendspt
dc.subjectMEH-PPVpt
dc.titleInterface morphology snapshots of vertically segregated thin films of semiconducting polymer/polystyrene blendsen
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionEMPA-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUniv São Paulo, Dept Fis & Matemat, FFCLRP, BR-14040901 Ribeirao Preto, SP, Brazil-
dc.description.affiliationEMPA, Swiss Fed Labs Mat Testing & Res, Lab Funct Polymers, CH-8600 Dubendorf, Switzerland-
dc.description.affiliationUNESP, Dept Fis, Fac Ciências, BR-17033360 Bauru, Brazil-
dc.description.affiliationUnespUNESP, Dept Fis, Fac Ciências, BR-17033360 Bauru, Brazil-
dc.identifier.doi10.1016/j.polymer.2007.02.059-
dc.identifier.wosWOS:000246330200024-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofPolymer-
dc.identifier.orcid0000-0003-0162-8273pt
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