Synthesis, characterization and field-effect transistor performance of poly[2,6-bis(3-alkylthiophen-2-yl)benzo[1,2-b;4,5-b']diselenophene]s
Articolo
Data di Pubblicazione:
2010
Citazione:
Synthesis, characterization and field-effect transistor performance of poly[2,6-bis(3-alkylthiophen-2-yl)benzo[1,2-b;4,5-b']diselenophene]s / M.A.M. Leenen, F. Vian, F. Cucinotta, W. Pisula, H. Thiem, R. Anselmann, L. De Cola. - In: MACROMOLECULAR CHEMISTRY AND PHYSICS. - ISSN 1022-1352. - 211:21(2010), pp. 2286-2291. [10.1002/macp.201000447]
Abstract:
Benzo[1,2-b:4,5-b']diselenophene (BDS) has been incorporated for the first time in a polymer. bis(Stannyl)-functionalized BDS was copolymerized with 3,3'-bis(alkyl)-5,5'-bithiophenes (dodecyl and tetradecyl side chains) through Stille copolymerization, to yield p-type polymer semiconductors for organic field-effect transistor application. The electronic and structural effect of the selenium atoms, compared to sulphur atoms in analogous copolymers, is described. The molecular weight has a decisive influence on the photophysical properties and supramolecular ordering, expressed in field-effect transistor measurements. Saturation mobilities around 10-2cm2• V-1s-1 are obtained on standard silicon substrates. Benzo[1,2-b:4,5-b']diselenophene-based copolymers have been synthesized by Stille copolymerization. The effect of the selenium atoms and the molecular weight on physical properties and field-effect transistor performance is discussed.
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
charge transport; conjugated polymers; photophysics; synthesis; wide-angle X-ray scattering (WAXS)
Elenco autori:
M.A.M. Leenen, F. Vian, F. Cucinotta, W. Pisula, H. Thiem, R. Anselmann, L. De Cola
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