Goldene

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Goldene is a 2-dimensional allotrope of gold. The thinnest commercial gold leaf is some 400 times thicker than goldene.[1] It features 9% lattice contraction compared to bulk gold.[1]

History[edit]

Goldene was first synthesized as a free-standing material in 2024 by a team at Linköping University in Sweden. A 2022 claim by a team at New York University Abu Dhabi has been disputed as actually containing multiple layers.[2]

Synthesis[edit]

The team used a material containing silicene between layers of titanium carbide. Gold layered on top of this combination diffused into the structure and replaced the silicon. Etching away the titanium carbide released free-standing goldene sheets that were up to 100 nanometres wide. The etching was performed using Murukami's reagent, in a 100-year-old technique used to decorate ironwork by Japanese blacksmiths. Surfactant molecules formed a barrier between goldene and the surrounding liquid — to stop the sheets from adhering.[2]

The team is exploring the potential for preparing goldene from other non-van der Waals Au-intercalated phases, including developing etching schemes.[1]

Graphene comparison[edit]

Forming 2D allotropes of metals such as gold has been difficult because metal atoms tend to cluster together and form nanoparticles instead of nanosheets.[2]

Properties[edit]

The material displayed Au 4f binding energy increase of 0.88 eV. The material is a semiconductor, with the valence band maximum 50 meV below the Fermi level.[1]

Applications[edit]

Potential applications included sensing and catalysis.

See also[edit]

References[edit]

  1. ^ a b c d Kashiwaya, Shun; Shi, Yuchen; Lu, Jun; Sangiovanni, Davide G.; Greczynski, Grzegorz; Magnuson, Martin; Andersson, Mike; Rosen, Johanna; Hultman, Lars (2024-04-16). "Synthesis of goldene comprising single-atom layer gold". Nature Synthesis: 1–8. doi:10.1038/s44160-024-00518-4. ISSN 2731-0582.
  2. ^ a b c Peplow, Mark (2024-04-18). "Meet 'goldene': this gilded cousin of graphene is also one atom thick". Nature. doi:10.1038/d41586-024-01118-0.

External links[edit]