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dc.contributor.authorRivnay, Jonathan
dc.contributor.authorSteyrleuthner, Robert
dc.contributor.authorJimison, Leslie H.
dc.contributor.authorCasadei, Alberto
dc.contributor.authorChen, Zhihua
dc.contributor.authorToney, Michael F.
dc.contributor.authorFacchetti, Antonio
dc.contributor.authorNeher, Dieter
dc.contributor.authorSalleo, Alberto
dc.date.accessioned2016-02-25T13:11:07Z
dc.date.available2016-02-25T13:11:07Z
dc.date.issued2011-07-12
dc.identifier.citationRivnay J, Steyrleuthner R, Jimison LH, Casadei A, Chen Z, et al. (2011) Drastic Control of Texture in a High Performance n-Type Polymeric Semiconductor and Implications for Charge Transport. Macromolecules 44: 5246–5255. Available: http://dx.doi.org/10.1021/ma200864s.
dc.identifier.issn0024-9297
dc.identifier.issn1520-5835
dc.identifier.doi10.1021/ma200864s
dc.identifier.urihttp://hdl.handle.net/10754/598020
dc.description.abstractControl of crystallographic texture from mostly face-on to edge-on is observed for the film morphology of the n-type semicrystalline polymer {[N,N-9-bis(2-octyldodecyl)naphthalene-1,4,5,8-bis(dicarboximide)-2,6-diyl] -alt-5,59-(2,29-bithiophene)}, P(NDI2OD-T2), when annealing the film to the polymer melting point followed by slow cooling to ambient temperature. A variety of X-ray diffraction analyses, including pole figure construction and Fourier transform peak shape deconvolution, are employed to quantify the texture change, relative degree of crystallinity and lattice order. We find that annealing the polymer film to the melt leads to a shift from 77.5% face-on to 94.6% edge-on lamellar texture as well as to a 2-fold increase in crystallinity and a 40% decrease in intracrystallite cumulative disorder. The texture change results in a significant drop in the electron-only diode current density through the film thickness upon melt annealing, while little change is observed in the in-plane transport of bottom gated thin film transistors. This suggests that the texture change is prevalent in the film interior and that either the (bottom) surface structure is different from the interior structure or the intracrystalline order and texture play a secondary role in transistor transport for this material. © 2011 American Chemical Society.
dc.description.sponsorshipPortions of this research were carried out at the Stanford Synchrotron Radiation Lightsource, a national user facility operated by Stanford University on behalf of the U.S. Department of Energy, Office of Basic Energy Sciences. A.S. and J.R. gratefully acknowledge financial support from the National Science Foundation in the form of respectively a Career Award and a Graduate Student Fellowship. A.C. gratefully acknowledges funding from Amber Capital Investment Management received through the Italian Scientists and Scholars of North America Foundation. This publication was partially based on work supported by the Center for Advanced Molecular Photovoltaics (Award No. KUS-C1-015-21), made by King Abdullah University of Science and Technology (KAUST). The work in Potsdam was financially supported by the German Federal Ministry of Science and Education (BMBF FKZ 03X3525D). We thank Dr. Eric Verploegen for use of the in-situ heating chamber at SSRL beamline 11-3 and Dr. Stefan Mannsfeld for providing the 2D GIXS analysis software WxDiff. Polyera Corp. thanks the FexTech Alliance for supporting the synthesis of P(NDI2OD-T2).
dc.publisherAmerican Chemical Society (ACS)
dc.titleDrastic Control of Texture in a High Performance n-Type Polymeric Semiconductor and Implications for Charge Transport
dc.typeArticle
dc.identifier.journalMacromolecules
dc.contributor.institutionStanford University, Palo Alto, United States
dc.contributor.institutionUniversitat Potsdam, Potsdam, Germany
dc.contributor.institutionAlma Mater Studiorum Universita di Bologna, Bologna, Italy
dc.contributor.institutionPolyera Corporation, Skokie, United States
dc.contributor.institutionStanford Synchrotron Radiation Laboratory, Menlo Park, United States
kaust.grant.numberKUS-C1-015-21
kaust.grant.fundedcenterCenter for Advanced Molecular Photovoltaics (CAMP)


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