4.8 Article

Hexagonal metal oxide monolayers derived from the metal-gas interface

Journal

NATURE MATERIALS
Volume 20, Issue 8, Pages 1073-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41563-020-00899-9

Keywords

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Funding

  1. Australian Research Council [DE160100715]
  2. McKenzie Fellowship programme
  3. National Natural Science Foundation of China [11904026]
  4. Beijing Natural Science Foundation [1194021]
  5. ARC Future Low Energy Electronics Technologies (FLEET) centre of excellence [CE170100039]

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Metal oxides as two-dimensional materials can be produced by cleavage of weak interlayer van der Waals bonds in layered bulk crystals, but obtaining pure and fully stoichiometric monolayers is challenging. Researchers have discovered a layered planar hexagonal phase of oxides from transition metals, post-transition metals, lanthanides and metalloids, which can be mechanically exfoliated without ionic dopants or vacancies, showing potential for further exploration in the 2D quantum regime.
Two-dimensional (2D) crystals are promising materials for developing future nano-enabled technologies(1-6). The cleavage of weak, interlayer van der Waals bonds in layered bulk crystals enables the production of high-quality 2D, atomically thin monolayers(7-10). Nonetheless, as earth-abundant compounds, metal oxides are rarely accessible as pure and fully stoichiometric monolayers owing to their ion-stabilized 'lamellar' bulk structure(11-14). Here, we report the discovery of a layered planar hexagonal phase of oxides from elements across the transition metals, post-transition metals, lanthanides and metalloids, derived from strictly controlled oxidation at the metal-gas interface. The highly crystalline monolayers, without the support of ionic dopants or vacancies, can easily be mechanically exfoliated by stamping them onto substrates. Monolayer and few-layered hexagonal TiO2 are characterized as examples, showing p-type semiconducting properties with hole mobilities of up to 950 cm(2) V-1 s(-1) at room temperature. The strategy can be readily extended to a variety of elements, possibly expanding the exploration of metal oxides in the 2D quantum regime.

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