Room-temperature epitaxy of metal thin films on tungsten diselenide

Kayla A. Cooley, Rajeh Alsaadi, Ramya L. Gurunathan, Anna C. Domask, Lauren Kerstetter, Wissam A. Saidi, Suzanne E. Mohney

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

The orientation of selected metals (Pd, Ni, Al, and Co) deposited on WSe2 by physical vapor deposition was examined using transmission electron microscopy and selected area electron diffraction. We discovered that Ni demonstrates room-temperature epitaxy, similarly to other face centered cubic (FCC) metals Au, Ag, and Cu. These epitaxial metals exhibit the following orientation relationship, where M stands for metal: M (111) || WSe2 (0001); M [22¯0] || WSe2 [112¯0]. Hexagonally close-packed Co, and FCC Pd and Al, were not epitaxial on deposition; however, Pd became epitaxial after annealing at 673 K for 5 h. To uncover critical variables for epitaxial growth, we correlated our experimental work and reports from the literature on Cu, Ag, and Au with density functional theory calculations of the energetics of metal atoms on the surface of WSe2 and thermodynamic calculations of metal-W-Se phase equilibria. Furthermore, we compared the findings to our previous work on metal/MoS2 systems to draw conclusions more generally applicable to epitaxial growth of metals on transition metal dichalcogenides (TMDs). We observed that epitaxy of metals on TMDs can occur when there is a match in crystallographic symmetry, even with a large lattice mismatch, and it is favored by metals exhibiting a low diffusion barrier on the TMD surface. However, reaction processes between the metal and WSe2 can prevent epitaxy even when the other factors are favorable, as occurred for Al/WSe2 with the formation of aluminum selenide, tungsten aluminide, and elemental tungsten. Consideration of crystallographic symmetry, surface diffusion barriers, and reactivity can be used to predict room-temperature epitaxy in other metal/TMD systems.
Original languageEnglish (US)
Pages (from-to)44-51
Number of pages8
JournalJournal of Crystal Growth
Volume505
DOIs
StatePublished - Jan 2019
Externally publishedYes

Bibliographical note

KAUST Repository Item: Exported on 2021-03-11
Acknowledgements: The computational work is supported in part by the University of Pittsburgh Center for Research Computing through the resources provided.

ASJC Scopus subject areas

  • Materials Chemistry
  • Inorganic Chemistry
  • Condensed Matter Physics

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