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dc.contributor.authorYao, Yuan-
dc.contributor.authorMetwalli, Ezzeldin-
dc.contributor.authorSu, Bo-
dc.contributor.authorKörstgens, Volker-
dc.contributor.authorMoseguí González, Daniel-
dc.contributor.authorMiasnikova, Anna-
dc.contributor.authorLaschewsky, Andre-
dc.contributor.authorOpel, Matthias-
dc.contributor.authorSantoro, Gonzalo-
dc.contributor.authorRoth, Stephan V.-
dc.contributor.authorMüller-Buschbaum, Peter-
dc.date.accessioned2019-05-29T11:44:21Z-
dc.date.available2019-05-29T11:44:21Z-
dc.date.issued2015-06-17-
dc.identifierdoi: 10.1021/acsami.5b03308-
dc.identifiere-issn: 1944-8252-
dc.identifierissn: 1944-8244-
dc.identifier.citationACS Applied Materials and Interfaces 7(23): 13080-13091 (2015)-
dc.identifier.urihttp://hdl.handle.net/10261/182778-
dc.description.abstractThe structure and magnetic behavior of hybrid films composed of maghemite (-Fe<inf>2</inf>O<inf>3</inf>) nanoparticles (NPs) and an asymmetric diblock copolymer (DBC) polystyrene<inf>61</inf>-block-polyN-isopropylacrylamide<inf>115</inf> are investigated. The NPs are coated with PS chains, which allow for a selective incorporation inside the PS domains at different NP concentrations. Upon incorporation of low amounts of NPs into the DBC thin films, the initial parallel (to film surface) cylinder morphology changes to a well ordered, perpendicularly oriented one. The characteristic domain distance of the DBC is increased due to the swelling of the PS domains with NPs. At higher NP concentrations, the excess NPs which can no longer be embedded in the PS domains, are accumulated at the film surface, and NP aggregates form. Irrespective of NP concentration, a superparamagnetic behavior of the metal oxide-DBC hybrid films is found. Such superparamagnetic properties make the established hybrid films interesting for high density magnetic storage media and thermoresponsive magnetic sensors.-
dc.description.sponsorshipThis work was supported by the BMBF (German Ministry of Research and Education) Grant No. 03DU03MU and by the Nanosystems Initiative Munich (NIM). Y.Y. and B.S. acknowledge the China Scholarship Council (CSC). V.K. thanks the Bavarian State Ministry of Education, Science and the Arts for funding this research work via project “Energy Valley Bavaria”.-
dc.publisherAmerican Chemical Society-
dc.relation.isversionofPublisher's version-
dc.rightsopenAccess-
dc.subjectMaghemite nanoparticles-
dc.subjectBlock copolymer-
dc.subjectNanocomposites-
dc.subjectHybrid films-
dc.subjectGISAXS-
dc.titleArrangement of Maghemite Nanoparticles via Wet Chemical Self-Assembly in PS- b -PNIPAM Diblock Copolymer Films-
dc.typeartículo-
dc.description.peerreviewedPeer reviewed-
dc.relation.publisherversionhttps://doi.org/10.1021/acsami.5b03308-
dc.date.updated2019-05-29T11:44:22Z-
dc.language.rfc3066eng-
dc.rights.licensehttp://creativecommons.org/licenses/by/4.0/-
dc.contributor.funderNanosystems Initiative Munich-
dc.contributor.funderChina Scholarship Council-
dc.contributor.funderBavarian State Ministry of Education, Science and the Arts-
dc.contributor.funderFederal Ministry of Education and Research (Germany)-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100002347es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004563es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004543es_ES
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