Quantifying Image Charge Effects in Molecular Tunnel Junctions Based on Self-Assembled Monolayers of Substituted Oligophenylene Ethynylene Dithiols

Zuoti Xie*, Valentin Diez Cabanes, Quyen Van Nguyen, Sandra Rodriguez-Gonzalez, Lucie Norel, Olivier Galangau, Stéphane Rigaut, Jérôme Cornil, C. Daniel Frisbie

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

A number of factors contribute to orbital energy alignment with respect to the Fermi level in molecular tunnel junctions. Here, we report a combined experimental and theoretical effort to quantify the effect of metal image potentials on the highest occupied molecular orbital to Fermi level offset, ϵh, for molecular junctions based on self-assembled monolayers (SAMs) of oligophenylene ethynylene dithiols (OPX) on Au. Our experimental approach involves the use of both transport and photoelectron spectroscopy to extract the offsets, ϵhtrans and ϵhUPS, respectively. We take the difference in these quantities to be the image potential energy eVimage. In the theoretical approach, we use density functional theory (DFT) to calculate directly eVimage between positive charge on an OPX molecule and the negative image charge in the Au. Both approaches yield eVimage ∼-0.1 eV per metal contact, meaning that the total image potential energy is a-0.2 eV for an assembled junction with two Au contacts. Thus, we find that the total image potential energy is 25-30% of the total offset ϵh, which means that image charge effects are significant in OPX junctions. Our methods should be generally applicable to understanding image charge effects as a function of molecular size, for example, in a variety of SAM-based junctions. © 2021 American Chemical Society.
Original languageEnglish
JournalACS applied materials & interfaces
DOIs
StatePublished - 16 Nov 2021

Keywords

  • molecular junction
  • tunneling
  • charge transport
  • image charge
  • Fermi level-HOMO offset
  • single level model
  • photoelectron spectroscopy

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