Nuclearity of Copper Clusters on hBN/SiC Heterostructure Modulates Molecular Adsorption

Abstract

Defect engineering can transform inert two-dimensional (2D) materials into chemically active and electronically tunable platforms by creating anchoring sites for metal atoms and clusters. Nevertheless, precise control over the formation, thermodynamic and kinetic stability, electronic structure, and chemical reactivity of metal species confined at these defect sites remains a challenge. Here, we use density functional theory (DFT) calculations assisted by machine-learning molecular dynamics (MLMD) simulations to elucidate the stability, electronic structure, and reactivity of Cu clusters anchored at boron vacancies (VB) in hBN/SiC heterostructures. Systematic variation of the Cu-to-vacancy ratio reveals a transition from isolated Cu atoms to multiatom Cu clusters at VB sites, with cluster growth reshaping the stability, electronic structure, and surface reactivity. Our results show that a single VB defect can be passivated by three Cu atoms, which compensate the local charge deficiency and stabilize the defect through Cu-N coordination. Capturing further Cu introduces localized midgap states that could influence the reactivity of the Cu-decorated defect sites. We probe the response of the Cu-decorated surface to chemically relevant gases CO, H2, O2, N2, H2S, and CO2, revealing implications for surface reactivity and stability. The calculations show pronounced cluster-size-dependent reactivity of Cu clusters at VB sites, with CO forming strong Cu-C bonds and O2 undergoing enhanced adsorption and molecular activation. Overall, this work identifies defect-engineered hBN/SiC as a versatile 2D platform for stabilizing Cu clusters and tuning gas-surface reactivity. By correlating Cu nuclearity at VB sites with electronic structure, molecular activation, and environmental robustness, our findings provide design guidelines for nuclearity-dependent metal functionalization of 2D heterostructures.