Issue 12, 2012

Solvent and polymermatrix effects on TIPS-pentacene/polymer blend organic field-effect transistors

Abstract

We report on a systematic study of solvent and polymer matrix effects on the phase segregation behavior of 6,13-bis(triisopropylsilylethynyl) pentacene (TIPS-pentacene) blends incorporated into two different amorphous polymer matrices, poly (α-methyl styrene) and poly (triarylamine), and using two solvents, chlorobenzene and tetralin. Optical microscopy, X-ray diffraction analyses, and optical absorption measurements are used to evaluate the film morphology, crystallinity, and optical density, respectively. These analyses are correlated with the extent of vertical segregation of TIPS-pentacene, as observed for the blended films by depth-profile XPS analyses. The microstructure and vertical phase segregation of TIPS-pentacene in blend films are found to be strongly influenced by the choice of solvent. Tetralin, a solvent with a high boiling temperature, was found to be more desirable for achieving distinct phase segregation/crystallization of TIPS-pentacene in blend films and best performance in OFETs with a dual-gate geometry. The electrical properties of top and bottom channels were consistent with the morphological characterization and OFETs processed from tetralin showed higher mobility values than those from chlorobenzene. Further modification of the annealing conditions in the TIPS-pentacene/PTAA/tetralin ternary system led to top-gate OFETs with mobility values up to 2.82 cm2/Vs.

Graphical abstract: Solvent and polymer matrix effects on TIPS-pentacene/polymer blend organic field-effect transistors

Supplementary files

Article information

Article type
Paper
Submitted
09 Dec 2011
Accepted
31 Jan 2012
First published
08 Feb 2012

J. Mater. Chem., 2012,22, 5531-5537

Solvent and polymer matrix effects on TIPS-pentacene/polymer blend organic field-effect transistors

D. K. Hwang, C. Fuentes-Hernandez, J. D. Berrigan, Y. Fang, J. Kim, W. J. Potscavage, H. Cheun, K. H. Sandhage and B. Kippelen, J. Mater. Chem., 2012, 22, 5531 DOI: 10.1039/C2JM16487F

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