One-Step Macroscopic Alignment of Conjugated Polymer Systems by Epitaxial Crystallization during Spin-Coating
Artikel i vetenskaplig tidskrift, 2013

The one-step preparation of highly anisotropic polymer semiconductor thin films directly from solution is demonstrated. The conjugated polymer poly(3-hexylthiophene) (P3HT) as well as P3HT:fullerene bulk–heterojunction blends can be spin-coated from a mixture of the crystallizable solvent 1,3,5-trichlorobenzene (TCB) and a second carrier solvent such as chlorobenzene. Solidification is initiated by growth of macroscopic TCB spherulites followed by epitaxial crystallization of P3HT on TCB crystals. Subsequent sublimation of TCB leaves behind a replica of the original TCB spherulites. Thus, highly ordered thin films are obtained, which feature square-centimeter-sized domains that are composed of one spherulite-like structure each. A combination of optical microscopy and polarized photoluminescence spectroscopy reveals radial alignment of the polymer backbone in case of P3HT, whereas P3HT:fullerene blends display a tangential orientation with respect to the center of spherulite-like structures. Moreover, grazing-incidence wide-angle X-ray scattering reveals an increased relative degree of crystallinity and predominantly flat-on conformation of P3HT crystallites in the blend. The use of other processing methods such as dip-coating is also feasible and offers uniaxial orientation of the macromolecule. Finally, the applicability of this method to a variety of other semi-crystalline conjugated polymer systems is established. Those include other poly(3-alkylthiophene)s, two polyfluorenes, the low band-gap polymer PCPDTBT, a diketopyrrolopyrrole (DPP) small molecule as well as a number of polymer:fullerene and polymer:polymer blends.

polymer semiconductors

fullerene

bulk–heterojunction

spherulite

nucleation

epitaxy

Författare

Christian Müller

Chalmers, Kemi- och bioteknik, Polymerteknologi

M. Aghamohammadi

Universitat Autonoma de Barcelona (UAB)

Scott Himmelberger

Stanford University

P. Sonar

Institute of Materials Research and Engineering, A-Star, Singapore

M. Garriga

Universitat Autonoma de Barcelona (UAB)

Alberto Salleo

Stanford University

M. Campoy-Quiles

Universitat Autonoma de Barcelona (UAB)

Advanced Functional Materials

1616-301X (ISSN)

Vol. 23 2368-2377

Ämneskategorier

Polymerteknologi

DOI

10.1002/adfm.201202983