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dc.contributor.authorReiser, Patrick
dc.contributor.authorBenneckendorf, Frank S.
dc.contributor.authorBarf, Marc-Michael
dc.contributor.authorMüller, Lars
dc.contributor.authorBäuerle, Rainer
dc.contributor.authorHillebrandt, Sabina
dc.contributor.authorBeck, Sebastian
dc.contributor.authorLovrincic, Robert
dc.contributor.authorMankel, Eric
dc.contributor.authorFreudenberg, Jan
dc.contributor.authorJänsch, Daniel
dc.contributor.authorKowalsky, Wolfgang
dc.contributor.authorPucci, Annemarie
dc.contributor.authorJaegermann, Wolfram
dc.contributor.authorBunz, Uwe H. F.
dc.contributor.authorMüllen, Klaus
dc.identifier.citationReiser , P , Benneckendorf , F S , Barf , M-M , Müller , L , Bäuerle , R , Hillebrandt , S , Beck , S , Lovrincic , R , Mankel , E , Freudenberg , J , Jänsch , D , Kowalsky , W , Pucci , A , Jaegermann , W , Bunz , U H F & Müllen , K 2019 , ' n-type doping of organic semiconductors : immobilization via covalent anchoring ' , Chemistry of Materials , vol. 31 , no. 11 , pp. 4213-4221 .
dc.identifier.otherPURE: 259453254
dc.identifier.otherPURE UUID: 6a79e9cc-dcb4-420c-9b57-45bc339908ac
dc.identifier.otherRIS: urn:8083857F8B682A73E1B3885C4D28F80E
dc.identifier.otherScopus: 85066493769
dc.identifier.otherWOS: 000471728200039
dc.descriptionWe gratefully acknowledge the German Federal Ministry of Education and Research (BMBF) for financial support within the InterPhase project (FKZ 13N13659, 13N13656, 13N13657, and 13N13658).en
dc.description.abstractElectrical doping is an important tool in the design of organic devices to modify charge carrier concentration in and Fermi level position of organic layers. The undesired diffusion of dopant molecules within common transport materials adversely affects both lifetime and device performance. To overcome this drawback, we developed a strategy to achieve immobilization of dopants through their covalent attachment to the semiconductor host molecules. Derivatization of the commonly employed n-type dopant 2-(2-methoxyphenyl)-1,3-dimethyl-2,3-dihydro-1H-benzoimidazole (ο-MeO-DMBI) with a phenylazide enables the resulting o-AzBnO-DMBI to photochemically generate a reactive nitrene, which subsequently binds covalently to the host material, 6,6-phenyl-C61-butyric acid methyl ester (PCBM). Both the activation and addition reactions are monitored by mass spectrometry as well as optical and photoelectron spectroscopy. A suppression of desorption and a decrease in volatility of the DMBI derivative in ultrahigh vacuum were observed after activation of a bilayer structure of PCBM and o-AzBnO-DMBI. Electrical measurements demonstrate that the immobilized o-AzBnO-DMBI can (i) dope the PCBM at conductivities comparable to values reported for o-MeO-DMBI in the literature and (ii) yield improved electrical stability measured in a lateral two terminal device geometry. Our immobilization strategy is not limited to the specific system presented herein but should also be applicable to other organic semiconductor–dopant combinations.
dc.relation.ispartofChemistry of Materialsen
dc.rightsCopyright © 2019 American Chemical Society. This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.en
dc.subjectQC Physicsen
dc.titlen-type doping of organic semiconductors : immobilization via covalent anchoringen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Physics and Astronomyen
dc.description.statusPeer revieweden

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