Self-assembly of poly(diethylhexyloxy-p-phenylenevinylene)-b-poly(4-vinylpyridine) rod-coil block copolymer systems
- Sary, Nicolas Department of Physics and Fribourg Center for Nanomaterials, University of Fribourg, Switzerland
- Rubatat, Laurent Department of Physics and Fribourg Center for Nanomaterials, University of Fribourg, Switzerland
- Brochon, Cyril Laboratoire d'Ingénierie des Polymères pour les Hautes Technologies, UMR 7165, Université Louis Pasteur, Strasbourg, France
- Hadziioannou, Georges Laboratoire d'Ingénierie des Polymères pour les Hautes Technologies, UMR 7165, Université Louis Pasteur, Strasbourg, France
- Ruokolainen, Janne Physics Laboratory, Helsinki University of Technology, Finland
- Mezzenga, Raffaele Nestlé Research Center, Lausanne, Switzerland - Department of Physics and Fribourg Center for Nanomaterials, University of Fribourg, Switzerland
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22.08.2007
Published in:
- Macromolecules. - 2007, vol. 40, no. 19, p. 6990 -6997
English
We describe the synthesis, the morphology, and self-assembly behavior of semiconducting poly(4-vinylpyridine-b-diethylhexyloxy-p-phenylenevinylene) (P4VP-b-PPV) rod-coil block copolymer systems. Three different block copolymers with 55%, 80%, and 88% coil volume fraction were synthesized by convergent anionic polymerization in THF using lithium α-methylstyrene as initiator. The morphology of the block copolymers was studied by transmission electron microscopy, small-angle X-ray scattering, and small-angle neutron scattering as a function of the volume fraction of the rod block as well as different annealing conditions. The microphase-separated morphologies in these block copolymers vary from lamellar, to hexagonal, and spherical, when the volume fraction of the rod is progressively reduced. By combining the lattice parameter measured by scattering techniques with the volume fraction of rod domains obtained by nuclear magnetic resonance, it was shown that the block copolymers in the lamellar structure are organized in a smectic C double layer, while in the hexagonal phase they self-organize in a homeotropic arrangement, with the rod blocks forming the dispersed phase. Furthermore, while self-assembly of rod-coil block copolymers in columnar hexagonal phase prevents close rod packing, for the lamellar phase evidence of this configuration among rods is shown by wide-angle X-ray scattering. As a consequence, the morphology and long-range order in the lamellar phase are the result of simultaneous inter-rods liquid crystalline interactions and the tendency to microphase segregation of rod and coil. As a result, depending on temperature, the lamellar phase can exist both with rods oriented in a smectic configuration and with randomly packed rods. We show that annealing the lamellar phase below its order-disorder transition temperature, TODT, but above the maximum affordable temperature for inter-rods liquid crystalline interactions, called smectic-in-lamellar to lamellar order-disorder transition temperature, TSL (with TSL<TODT), leads to highly improved long-range lamellar order, which is then preserved when the system is cooled below TSL, at which temperature rod close packing is fully recovered.
- Faculty
- Faculté des sciences et de médecine
- Department
- Département de Physique
- Language
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- English
- Classification
- Physics
- License
- License undefined
- Identifiers
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- RERO DOC 9403
- DOI 10.1021/ma0710885
- Persistent URL
- https://folia.unifr.ch/unifr/documents/300696
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