Two-dimensional charge transport in self-organized, high-mobility conjugated polymers
H. Sirringhaus (),
P. J. Brown,
R. H. Friend,
M. M. Nielsen,
K. Bechgaard,
B. M. W. Langeveld-Voss,
A. J. H. Spiering,
R. A. J. Janssen,
E. W. Meijer,
P. Herwig and
D. M. de Leeuw
Additional contact information
H. Sirringhaus: Cavendish Laboratory, University of Cambridge
P. J. Brown: Cavendish Laboratory, University of Cambridge
R. H. Friend: Cavendish Laboratory, University of Cambridge
M. M. Nielsen: Risø National Laboratory
K. Bechgaard: Risø National Laboratory
B. M. W. Langeveld-Voss: Laboratory of Macromolecular and Organic Chemistry, Eindhoven University of Technology
A. J. H. Spiering: Laboratory of Macromolecular and Organic Chemistry, Eindhoven University of Technology
R. A. J. Janssen: Laboratory of Macromolecular and Organic Chemistry, Eindhoven University of Technology
E. W. Meijer: Laboratory of Macromolecular and Organic Chemistry, Eindhoven University of Technology
P. Herwig: Philips Research Laboratories
D. M. de Leeuw: Philips Research Laboratories
Nature, 1999, vol. 401, issue 6754, 685-688
Abstract:
Abstract Self-organization in many solution-processed, semiconducting conjugated polymers results in complex microstructures, in which ordered microcrystalline domains are embedded in an amorphous matrix1. This has important consequences for electrical properties of these materials: charge transport is usually limited by the most difficult hopping processes and is therefore dominated by the disordered matrix, resulting in low charge-carrier mobilities2 (⩽10-5 cm2 V-1 s-1). Here we use thin-film, field-effect transistor structures to probe the transport properties of the ordered microcrystalline domains in the conjugated polymer poly(3-hexylthiophene), P3HT. Self-organization in P3HT results in a lamella structure with two-dimensional conjugated sheets formed by interchain stacking. We find that, depending on processing conditions, the lamellae can adopt two different orientations—parallel and normal to the substrate—the mobilities of which differ by more than a factor of 100, and can reach values as high as 0.1 cm2 V-1 s-1 (refs 3, 4). Optical spectroscopy of the field-induced charge, combined with the mobility anisotropy, reveals the two-dimensional interchain character of the polaronic charge carriers, which exhibit lower relaxation energies than the corresponding radical cations on isolated one-dimensional chains. The possibility of achieving high mobilities via two-dimensional transport in self-organized conjugated lamellae is important for applications of polymer transistors in logic circuits5 and active-matrix displays4,6.
Date: 1999
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DOI: 10.1038/44359
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