Band formation at interfaces between N-heteropolycycles and gold electrodes

Efficient charge injection at organic semiconductor/metal interfaces is crucial for the performance of organic field effect transistors. Interfacial hybrid band formation between electronic states of the organic compound and the metal electrode facilitates effective charge injection. Here, we show t...

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Hauptverfasser: Stein, Arnulf (VerfasserIn) , Rolf, Daniela (VerfasserIn) , Lotze, Christian (VerfasserIn) , Günther, Benjamin (VerfasserIn) , Gade, Lutz H. (VerfasserIn) , Franke, Katharina J. (VerfasserIn) , Tegeder, Petra (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: January 13, 2021
In: The journal of physical chemistry letters
Year: 2021, Jahrgang: 12, Heft: 2, Pages: 947-951
ISSN:1948-7185
DOI:10.1021/acs.jpclett.0c03630
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/acs.jpclett.0c03630
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Verfasserangaben:Arnulf Stein, Daniela Rolf, Christian Lotze, Benjamin Günther, Lutz H. Gade, Katharina J. Franke, and Petra Tegeder
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Zusammenfassung:Efficient charge injection at organic semiconductor/metal interfaces is crucial for the performance of organic field effect transistors. Interfacial hybrid band formation between electronic states of the organic compound and the metal electrode facilitates effective charge injection. Here, we show that a long-range ordered monolayer of a flat-lying N-heteropolycyclic aromatic compound on Au(111) leads to dispersing occupied and unoccupied interfacial hybrid bands. Using angle-resolved two-photon photoemission we determine their energy level alignment and dispersion relations. We suggest that band formation proceeds via hybridization of a localized occupied molecular state with the d-bands of the Au substrate, where the large effective mass of the d-bands is significantly reduced in the hybrid band. Hybridization of an unoccupied molecular state with the Au sp-band leads to a band with an even smaller effective mass.
Beschreibung:Gesehen am 10.09.2021
Beschreibung:Online Resource
ISSN:1948-7185
DOI:10.1021/acs.jpclett.0c03630