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Selective inclusion of chromophore molecules into poly(styrene-b-methylmethacrylate) block copolymer nanodomains: a study of morphological, optical and electrical properties

TitleSelective inclusion of chromophore molecules into poly(styrene-b-methylmethacrylate) block copolymer nanodomains: a study of morphological, optical and electrical properties
Publication TypeArticolo su Rivista peer-reviewed
Year of Publication2015
AuthorsDiletto, C., Morvillo Pasquale, Di Girolamo R., Auriemma F., and De Rosa C.
JournalJournal of Sol-Gel Science and Technology
Volume73
Pagination634-640
ISSN09280707
Keywords6]-phenyl-C61-butyric acid methyl esters, Block copolymers, butyric acid, Chromophores, Copolymers, Film preparation, Indium thin oxides, Innovative approaches, Lamellar morphology, Methyl methacrylates, Molecules, Nanocomposites, Optical and electrical properties, Oxide films, Polymer matrix composites, Selective inclusion, Selective incorporations, styrene, [6
Abstract

Innovative nanocomposites based on a nanostructured block copolymer (BCP) matrix whose lamellar nanodomains are selectively loaded with organic molecules, were prepared. A symmetric poly(styrene-b-methylmethacrylate) (PS-b-PMMA) amorphous BCP showing a lamellar morphology was employed. Thin films of PS-b-PMMA were deposited by spin-coating on indium thin oxide (ITO) substrate in order to achieve orientation of lamellae with the lamellar surface perpendicular to the substrate. Nanocomposites were then prepared by selective incorporation of [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) molecules into the PS lamellar domain. The self-assembly of the BCP generated the nanotemplate to selectively control the spatial location of the PCBM molecules, in which the apolar properties of PS block provided the physical stabilization for achieving uniform PCBM distribution. These innovative approaches can be utilized as a tool to realize memory devices. © 2014, Springer Science+Business Media New York.

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URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84925535110&doi=10.1007%2fs10971-014-3572-5&partnerID=40&md5=88a9e3b15480ba8c4871f8fa90ebfe5e
DOI10.1007/s10971-014-3572-5
Citation KeyDiletto2015634