Abstract

Graphene and hexagonal boron nitride (h-BN), as typical two-dimensional (2D) materials, have long attracted substantial attention due to their unique properties and promise in a wide range of applications. Although they have a rather large difference in their intrinsic bandgaps, they share a very similar atomic lattice; thus, there is great potential in constructing heterostructures by lateral stitching. Herein, we present the in situ growth of graphene and h-BN lateral heterostructures with tunable morphologies that range from a regular hexagon to highly symmetrical star-like structure on the surface of liquid Cu. The chemical vapor deposition (CVD) method is used, where the growth of the h-BN is demonstrated to be highly templated by the graphene. Furthermore, large-area production of lateral G-h-BN heterostructures at the centimeter scale with uniform orientation is realized by precisely tuning the CVD conditions. We found that the growth of h-BN is determined by the initial graphene and symmetrical features are produced that demonstrate heteroepitaxy. Simulations based on the phase field and density functional theories are carried out to elucidate the growth processes of G-h-BN flakes with various morphologies, and they have a striking consistency with experimental observations. The growth of a lateral G-h-BN heterostructure and an understanding of the growth mechanism can accelerate the construction of various heterostructures based on 2D materials.

Highlights

  • Conventional heteroepitaxy refers to the formation of an extended single-crystal film on the two-dimensional (2D) surface of a single crystal of a different material, as exemplified by the growth of GaP on Si1,2

  • We report the in situ growth of graphene and hBN lateral heterostructures with a tunable morphology on a liquid Cu surface by the chemical vapor deposition (CVD) method, where the highly templated growth of hexagonal boron nitride (h-BN) induced by pregrown graphene crystals is demonstrated

  • Theoretical calculations based on phase field theory (PFT) are conducted to probe the morphology evolution of the h-BN domains grown from a graphene seed crystal and the results are consistent with the experimental observations

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Summary

Introduction

Conventional heteroepitaxy refers to the formation of an extended single-crystal film on the two-dimensional (2D) surface of a single crystal of a different material, as exemplified by the growth of GaP on Si1,2. The atomic lattice of the surface can act as a template for the initial growth of the epilayer if the different materials have similar lattice constants. As two typical 2D materials, graphene (G) and hexagonal boron nitride (h-BN), have fueled enormous interest; importantly, they have similar crystal structures with a lattice constant mismatch of only 2% and possess great promise in constructing in-plane heterostructures via heteroepitaxial growth[3,4]. We report the in situ growth of graphene and hBN lateral heterostructures with a tunable morphology on a liquid Cu surface by the CVD method, where the highly templated growth of h-BN induced by pregrown graphene crystals is demonstrated. It is found that the subsequent growth of the h-BN is templated by the inner graphene, resulting in morphology engineering of the hBN by modulating the CVD conditions. Theoretical calculations based on phase field theory (PFT) are conducted to probe the morphology evolution of the h-BN domains grown from a graphene seed crystal and the results are consistent with the experimental observations

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