Fruitful discussions with Dr. Bernard Lotz, Dr. Marc Schmutz, and Dr. Jean-Claude Wittmann are gratefully acknowledged. We also thank Dr. Tony Jenkins (Merck Chemicals Ltd.) for kindly providing one of the P3HT samples used in this study. Dr. Christian Chaumont is gratefully acknowledged for performing the XRD measurements on oriented TCB thin films. Supporting Information is available online from Wiley InterScience or from the author.
Effect of Molecular Weight on the Structure and Morphology of Oriented Thin Films of Regioregular Poly(3-hexylthiophene) Grown by Directional Epitaxial Solidification†
Article first published online: 29 NOV 2006
Copyright © 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Advanced Functional Materials
Volume 17, Issue 1, pages 101–108, January, 2007
How to Cite
Brinkmann, M. and Rannou, P. (2007), Effect of Molecular Weight on the Structure and Morphology of Oriented Thin Films of Regioregular Poly(3-hexylthiophene) Grown by Directional Epitaxial Solidification. Adv. Funct. Mater., 17: 101–108. doi: 10.1002/adfm.200600673
- Issue published online: 4 JAN 2007
- Article first published online: 29 NOV 2006
- Manuscript Revised: 13 SEP 2006
- Manuscript Received: 27 JUL 2006
- Epitaxial growth;
- Polymeric materials;
- Thin films, polymer
Regioregular head-to-tail (HT)-coupled poly(3-hexylthiophene-2,5-diyl) (P3HT) with a weight-average molecular weight (Mw) in the 7.3–69.6 kDa range is crystallized by directional epitaxial solidification in 1,3,5-trichlorobenzene (TCB) to yield highly oriented thin films. An oriented and periodic lamellar structure consisting of crystalline lamellae separated by amorphous interlamellar zones is evidenced by atomic force microscopy (AFM) and transmission electron microscopy (TEM). Both the overall crystallinity as well as the orientation of the crystalline lamellae decrease significantly with increasing Mw. The total lamellar periodicity is close to the length of “fully extended” chains for Mw = 7.3 kDa (polystyrene-equivalent molecular weight, eq. PS) and it saturates to a value of ca. (25–28) ± 2 nm for Mw ≥ 18.8 kDa (eq. PS). This behavior is attributed to a transition from an oligomeric-like system, for which P3HT chains are essentially in a fully extended all-trans conformation and do not fold, to a semicrystalline system that involves a periodic alternation of crystalline lamellae separated by extended amorphous interlamellar zones, which harbor chain folds, chain ends, and tie molecules. For P3HT with Mw of ca. 7.3 kDa (eq. PS), epitaxial crystallization on TCB allows for the growth of both “edge-on” and “flat-on” oriented crystalline lamellae on the TCB substrate. The orientation of the lamellae is attributed to 1D epitaxy. Because of the large size of the “flat-on” crystalline lamellae, a characteristic single-crystal electron diffraction pattern corresponding to the  zone was obtained by selected area electron diffraction (SAED), indicating that P3HT crystallizes in a monoclinic unit cell with a = 16.0 Å, b = 7.8 Å, c = 7.8 Å, and γ = 93.5°.