A quantitative correlation between the mobility and crystallinity of photo-cross-linkable P3HT
KAUST DepartmentChemical Science Program
Office of the VP
Physical Science and Engineering (PSE) Division
Online Publication Date2012-03-20
Print Publication Date2012-04-10
Permanent link to this recordhttp://hdl.handle.net/10754/562152
MetadataShow full item record
AbstractThe performance of polymer field effect transistors (FETs) can vary by orders of magnitude by applying different processing conditions. Although it is generally believed that a higher degree of crystallinity results in a higher mobility, the correlation is not straightforward. In addition, the effect of cross-linking on polymer thin film microstructural order is relatively unknown. This study investigates the effect of thermal annealing and UV-initiated photo-cross-linking on the FET performance and microstructural order of a photo-cross-linkable P3HT derivative. Our results demonstrate that while cross-linking did not disrupt the overall crystallinity of the polymer thin film, the photo-cross-linking process likely induced doping in the semiconductor layer, leading to the absence of saturation behavior in the FET. Annealing after cross-linking slightly improved the FET performance but only minimally affected the microstructural order of the polymer film since the 3D morphology had been "locked in" during the first cross-linking step. Importantly, annealing and cross-linking simultaneously was a successful method to preserve polymer crystallinity while also achieving effective cross-linking. Using newly developed quantitative X-ray analysis techniques, our study established a quantitative correlation between FET charge mobility and thin film crystallinity. © 2012 American Chemical Society.
SponsorsThe authors acknowledge financial support by the U.S. Department of Energy, Basic Energy Sciences, under Contract DE-AC03-76SF00098. Partial support from the Frechet "other donors" fund is also acknowledged. C.H.W. and T.W.H. thank the National Science Foundation for Graduate Research Fellowships. Portions of this research were carried out at the Stanford Synchrotron Radiation Laboratory, a national user facility operated by Stanford University on behalf of the U.S. Department of Energy, Office of Basic Energy Sciences. The authors also thank Leslie Jimison and Jonathan Rivnay for helpful discussions.
PublisherAmerican Chemical Society (ACS)