Pathways toward controlled assembly of functional polymer-based nanostructures

 |  Login

Show simple item record

dc.contributor Aalto-yliopisto fi
dc.contributor Aalto University en
dc.contributor.author Laiho, Ari
dc.date.accessioned 2012-08-21T12:35:14Z
dc.date.available 2012-08-21T12:35:14Z
dc.date.issued 2009
dc.identifier.isbn 978-951-22-9815-0
dc.identifier.isbn 978-951-22-9814-3 (printed) #8195;
dc.identifier.issn 1795-4584
dc.identifier.uri https://aaltodoc.aalto.fi/handle/123456789/4599
dc.description.abstract This thesis deals with a common drawback that is often encountered in self-assembled nanostructured soft matter. Even though spontaneous self-assembly can be used to create diverse nanostructures, the structures, as such, are typically polydomain, consisting of locally ordered small domains that lack mutual orientation and/or long range correlation. As a result, the material remains macroscopically isotropic and disordered. The aim here is to explore feasible ways, on one hand, to control the assembly and, on the other hand, to obtain macroscopically anisotropic materials and functions. We show the first example of how charge-transfer complexation between C60 fullerenes and electron-donating units of block copolymers can enable control of the morphology and properties of fullerene based materials. We also study the alignment of randomly oriented domains of nanostructured material over macroscopic length scales by using a real-time rheo-optical apparatus in combination with more detailed ex-situ structural characterization. Alignment of randomly oriented domains is not only useful for obtaining macroscopically anisotropic materials and functions but it can also be a prerequisite for detailed characterization of the local structures. This aspect is demonstrated for hierarchical liquid crystalline (LC) diblock copolymer structures which, upon inducing shear alignment, exhibit coexistence of two orthogonal orientations of the LC phase within the copolymer lamellae. Furthermore we demonstrate that ionic complexes forming a columnar LC phase can be efficiently aligned within polymer blends upon shearing, taken that the matrix polymers have sufficiently high molecular weight. This concept allows a simple route for macroscopically aligned nanocomposites with conjugated columnar LC functional additives. Finally, control of the nanoscale morphology in polymer/fullerene nanocomposite thin film devices is shown to allow tuning of the electrical switching that can enable construction of a memory unit. The working principles of such thin film organic memory devices have remained debated and the first systematic approach is here undertaken to tailor the active material composition and to study the morphology vs. functionality relationship. en
dc.format.extent Verkkokirja (7349 KB, 50 s.)
dc.format.mimetype application/pdf
dc.language.iso en en
dc.publisher Teknillinen korkeakoulu en
dc.relation.ispartofseries TKK dissertations, 156 en
dc.relation.haspart [Publication 1]: Ari Laiho, Robin H. A. Ras, Sami Valkama, Janne Ruokolainen, Ronald Österbacka, and Olli Ikkala. 2006. Control of self-assembly by charge-transfer complexation between C60 fullerene and electron donating units of block copolymers. Macromolecules, volume 39, number 22, pages 7648-7653. en
dc.relation.haspart [Publication 2]: Ari Laiho and Olli Ikkala. 2007. A rheo-optical apparatus for real time kinetic studies on shear-induced alignment of self-assembled soft matter with small sample volumes. Review of Scientific Instruments, volume 78, number 1, 015109. © 2007 American Institute of Physics. By permission. en
dc.relation.haspart [Publication 3]: Ari Laiho, Panu Hiekkataipale, Janne Ruokolainen, and Olli Ikkala. 2009. Coexisting parallel and perpendicular orientations of smectic layers within copolymer lamellae in a shear aligned liquid crystalline diblock copolymer. Helsinki University of Technology Publications in Engineering Physics, Report TKK-F-A856. Macromolecular Chemistry and Physics, submitted for publication. en
dc.relation.haspart [Publication 4]: Ari Laiho, Bernd M. Smarsly, Charl F. J. Faul, and Olli Ikkala. 2008. Macroscopically aligned ionic self-assembled perylene-surfactant complexes within a polymer matrix. Advanced Functional Materials, volume 18, number 13, pages 1890-1897. © 2008 Wiley-VCH Verlag. By permission. en
dc.relation.haspart [Publication 5]: Jayanta K. Baral, Himadri S. Majumdar, Ari Laiho, Hua Jiang, Esko I. Kauppinen, Robin H. A. Ras, Janne Ruokolainen, Olli Ikkala, and Ronald Österbacka. 2008. Organic memory using [6,6]-phenyl-C61 butyric acid methyl ester: morphology, thickness and concentration dependence studies. Nanotechnology, volume 19, number 3, 035203. © 2008 Institute of Physics Publishing. By permission. en
dc.relation.haspart [Publication 6]: Ari Laiho, Himadri S. Majumdar, Jayanta K. Baral, Fredrik Jansson, Ronald Österbacka, and Olli Ikkala. 2008. Tuning the electrical switching of polymer/fullerene nanocomposite thin film devices by control of morphology. Applied Physics Letters, volume 93, number 20, 203309. © 2008 American Institute of Physics. By permission. en
dc.subject.other Physics en
dc.title Pathways toward controlled assembly of functional polymer-based nanostructures en
dc.type G5 Artikkeliväitöskirja fi
dc.contributor.department Teknillisen fysiikan laitos fi
dc.subject.keyword self-assembly en
dc.subject.keyword shear alignment en
dc.subject.keyword block copolymer en
dc.subject.keyword fullerene en
dc.subject.keyword organic electronics en
dc.identifier.urn URN:ISBN:978-951-22-9815-0
dc.type.dcmitype text en
dc.type.ontasot Väitöskirja (artikkeli) fi
dc.type.ontasot Doctoral dissertation (article-based) en


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search archive


Advanced Search

article-iconSubmit a publication

Browse

My Account