Abstract

The understanding of the metal and transition metal dichalcogenide (TMD) interface is critical for future electronic device technologies based on this new class of two-dimensional semiconductors. Here, we investigate the initial growth of nanometer-thick Pd, Au, and Ag films on monolayer MoS<sub>2</sub>. Distinct growth morphologies are identified by atomic force microscopy: Pd forms a uniform contact, Au clusters into nanostructures, and Ag forms randomly distributed islands on MoS<sub>2</sub>. The formation of these different interfaces is elucidated by large-scale spin-polarized density functional theory calculations. Using Raman spectroscopy, we find that the interface homogeneity shows characteristic Raman shifts in E<sub>2g</sub><sup>1</sup> and A<sub>1g</sub> modes. Interestingly, we show that insertion of graphene between metal and MoS<sub>2</sub> can effectively decouple MoS<sub>2</sub> from the perturbations imparted by metal contacts (<i>e.g.</i>, strain), while maintaining an effective electronic coupling between metal contact and MoS<sub>2</sub>, suggesting that graphene can act as a conductive buffer layer in TMD electronics.

Keywords:
Monolayer Graphene Metal Raman spectroscopy Density functional theory Electrical conductor Transition metal Homogeneity (statistics)

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Topics

2D Materials and Applications
Physical Sciences →  Materials Science →  Materials Chemistry
Graphene research and applications
Physical Sciences →  Materials Science →  Materials Chemistry
Surface and Thin Film Phenomena
Physical Sciences →  Physics and Astronomy →  Atomic and Molecular Physics, and Optics

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