Can We Predict Interface Dipoles Based on Molecular Properties?

Johannes Cartus, Andreas Jeindl, Oliver Hofmann*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

We apply high-throughput density functional theory calculations and symbolic regression to hybrid inorganic/organic interfaces with the intent to extract physically meaningful correlations between the adsorption-induced work function modifications and the properties of the constituents. We separately investigate two cases: (1) hypothetical, free-standing self-assembled monolayers with a large intrinsic dipole moment and (2) metal–organic interfaces with a large charge-transfer-induced dipole. For the former, we find, without notable prior assumptions, the Topping model, as expected from the literature. For the latter, highly accurate correlations are found, which are, however, clearly unphysical.
Original languageEnglish
Pages (from-to)32270-32276
Number of pages7
JournalACS Omega
Volume6
Issue number47
DOIs
Publication statusPublished - 30 Nov 2021

ASJC Scopus subject areas

  • Chemical Engineering(all)
  • Chemistry(all)

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