Metallic Hydrogen in Atomically Precise Gold Nanoclusters

Guoxiang Hu, Qing Tang, Dongil Lee, Zili Wu, De En Jiang

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31 Citations (Scopus)

Abstract

Hydrogen-metal interaction is the foundation of many technologies and processes, but how hydrogen behaves in atomically precise gold nanoclusters remains unknown even though they have been used in hydrogenation catalysis and water splitting. Herein, we investigate how hydrogen interacts with [Au25(SR)18]q clusters and mono-atom-doped bimetallic [M1Au24(SR)18]q clusters (M = Pt, Pd, Ag, Cu, Hg, or Cd) from first principles. We find that hydrogen behaves as a metal in these clusters and contributes its 1s electron to the superatomic free-electron count. This opposite behavior compared to that of the hydride in Cu and Ag clusters allows the small hydrogen to interstitially dope the gold clusters and tune their superatomic electronic structure. The doping energetics shows that when an eight-electron superatom is formed after H doping, the binding energy of H is much stronger, while binding of H with an already eight-electron superatom is much weaker. Indeed, frontier orbitals and the HOMO-LUMO gaps of [Au25H1(SR)18]0, [Au25H2(SR)18]+, [PtAu24H2(SR)18]0, [PdAu24H2(SR)18]0, [AgAu24H(SR)18]0, and [CuAu24H(SR)18]0 all have very similar features, because they are all eight-electron superatoms. By calculating the Gibbs free energies of hydrogen adsorption, we predict that PtAu24(SR)18, PdAu24(SR)18, and center-doped CuAu24(SR)18 can be good electrocatalysts for the hydrogen evolution reaction.

Original languageEnglish
Pages (from-to)4840-4847
Number of pages8
JournalChemistry of Materials
Volume29
Issue number11
DOIs
Publication statusPublished - 2017 Jun 13

Bibliographical note

Funding Information:
This research is sponsored by the U.S. Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division. D.L. acknowledges support by a Korea CCS R&D Center (KCRC) grant (NRF-2014M1A8A1074219) and NRF grants (NRF- 2014R1A2A1A11051032 and 2009-0093823). This research used resources of the National Energy Research Scientific Computing Center, a DOE Office of Science User Facility supported by the Office of Science of the U.S. Department of Energy under Contract DE-AC02-05CH11231.

All Science Journal Classification (ASJC) codes

  • Chemistry(all)
  • Chemical Engineering(all)
  • Materials Chemistry

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