Abstract

This photoemission study shows that the work function (Φ) of indium–tin-oxide (ITO) can be increased from 4.2 up to 6.5 eV upon the deposition of the molecular electron acceptors tetrafluoro-tetracyanoquinodimethane (F4TCNQ) and hexaazatriphenylene-hexacarbonitrile (HATCN). The evolution of sample Φ and the hole injection barrier upon subsequent deposition of the hole transport material <i>N</i>,<i>N</i>′-bis­(1-naphthyl)-<i>N</i>,<i>N</i>′-diphenyl-1,1′-biphenyl-4,4′-diamine (α-NPD) was studied for different acceptor precoverages of ITO, corresponding to different initial Φ values. When Φ of the acceptor covered substrate exceeds a critical value Φ<sub>crit</sub>, the highest occupied molecular level of multilayer α-NPD is found to be pinned 0.5 eV below the Fermi level (E<sub>F</sub>). Noteworthy, Φ<sub>crit</sub> is found at 5.2 eV, which is 0.4 eV higher than expected for α-NPD (4.8 eV), and vacuum level alignment does not apply even before E<sub>F</sub>-pinning sets in. An electrostatic model that accounts for nonuniformity of the substrate at acceptor submonolayer coverages and the associated local work function changes explains the origin of “delayed” E<sub>F</sub>-pinning

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