Phase Variations and Layer Epitaxy of 2D PdSe₂ Grown on 2D Monolayers by Direct Selenization of Molecular Pd Precursors.

Abstract

Two-dimensional (2D) materials and van der Waals heterostructures with atomic-scale thickness provide enormous potential for advanced science and technology. However, insufficient knowledge of compatible synthesis impedes wafer-scale production. PdSe₂ and Pd₂Se₃ are two of the noble transition-metal chalcogenides with excellent physical properties that have recently emerged as promising materials for electronics, optoelectronics, catalyst, and sensors. This research presents a feasible approach to synthesize PdSe₂ and Pd₂Se₃ with inherently asymmetric structure on honeycomb lattice 2D monolayer substrates of graphene and MoS₂. We directly deposit a molecular transition-metal precursor complex on the surface of the 2D substrates, followed by low-temperature selenization by chemical vapor flow. Parameter control leads to tuning of the material from monolayer nanocrystals with Pd₂Se₃ phase, to continuous few-layer PdSe₂ films. Annular dark-field scanning transmission electron microscopy (ADF-STEM) reveals the structure, phase variations, and heteroepitaxy at the atomic level. PdSe₂ with unconventional interlayer stacking shifts appeared as the kinetic product, whereas the bilayer PdSe₂ and monolayer Pd₂Se₃ are the thermodynamic product. The epitaxial alignment of interlayer rotation and translation between the PdSe₂ and underlying 2D substrate was also revealed by ADF-STEM. These results offer both nanoscale and atomic-level insights into direct growth of van der Waals heterostructures, as well as an innovative method for 2D synthesis by predetermined nucleation.