Web Release Date: January 15,
Enhancement of Field-Effect Mobility and Stability of Poly(3-hexylthiophene) Field-Effect Transistors by Conformational Change
Department of Chemical Engineering, Pohang University of Science and Technology, Pohang, 790-784, Korea
Received: September 5, 2007
In Final Form: October 27, 2007
Abstract:
With the aim of enhancing the field-effect mobility and air stability of self-aligned regioregular poly(3-hexylthiophene), P3HT, by promoting two-dimensional molecular ordering, we transformed the chemical structure of the P3HT chain from a benzoid to a quinoid structure by doping the P3HT solution with HAuCl4 prior to film formation. We found that, for the appropriate HAuCl4 concentration, the P3HT nanocrystals adopt a highly ordered molecular structure with a field-effect mobility of 0.03 cm2 V-1 s-1, which is an improvement by a factor of more than 100. This increase in field-effect mobility is due to a significant enhancement of molecular ordering and the perpendicular orientation of the nanocrystals with respect to the insulator substrate. This resulted from the change in the P3HT chain conformation from a benzoid to a quinoid structure due to oxidation by HAuCl4. The quinoid structure favors a linear or expanded-coil conformation, so the thiophene inter-ring bonds have increased double-bond character, which improves the molecular ordering. Furthermore, the electrical properties of a doped P3HT device had highly improved stability to air without encapsulation. These results suggest that the effect of unintentional doping by oxygen on HAuCl4-doped P3HT film is insignificant because the p-type doping effect of HAuCl4 is the major contributor.
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