Charge-induced dipole vs. relativistically enhanced covalent interactions in Ar-tagged Au-Ag tetramers and pentamers

A. Shayeghi*, R. Schäfer, D. M. Rayner, R. L. Johnston, A. Fielicke

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

22 Citations (Scopus)
246 Downloads (Pure)

Abstract

Vibrational spectra of Au n Ag m + · Ar k (n + m = 4, 5; k = 1-4) clusters are determined by far-infrared resonant multiple photon dissociation spectroscopy in the range ν = 100 -250 cm<sup>-1</sup>. The experimental spectra are assigned using density functional theory for geometries obtained by the Birmingham cluster genetic algorithm. Putative global minimum candidates of the Ar complexes are generated by adding Ar atoms to the Au n Ag m + low energy isomers and subsequent local optimization. Differential Ar binding energies indicate exceptionally strong Au-Ar bonds in Au-rich clusters, leading to fundamental changes to the IR spectra. The stronger Ar binding is attributed to a relativistically enhanced covalent character of the Au-Ar bond, while in Au-rich species charge-induced dipole interactions overcompensate the relativistic affinity to Au. Moreover, not only the absolute composition but also the topologies are essential in the description of Ar binding to a certain cluster.

Original languageEnglish
Article number024310
JournalJournal of Chemical Physics
Volume143
Issue number2
DOIs
Publication statusPublished - 14 Jul 2015

ASJC Scopus subject areas

  • General Physics and Astronomy
  • Physical and Theoretical Chemistry

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