The surface phase diagram of Fe₃O₄(001) revisited

Abstract

Understanding how the physical and electronic structures of metal-oxide surfaces evolve under varying conditions is crucial for optimizing their performance in applications such as catalysis. In this study, we compute the surface phase diagram of the Fe₃O₄(001) facet using density functional theory (DFT)-based calculations, with an emphasis on understanding the terminations observed in surface science experiments. Our results reveal two stable terminations in addition to the subsurface cation vacancy (SCV) structure, which dominates under oxidizing conditions. The commonly reported octahedral Fe pair, also known as the Fe-dimer termination, is stable within an oxygen chemical potential range of −3.1 eV < μₒ < −2.3 eV. We identify the lowest-energy structure of this surface as the one proposed by J. R. Rustad, E. Wasserman and A. R. Felmy, A Molecular Dynamics Investigation of Surface Reconstruction on Magnetite (001), Surf. Sci., 1999, 432, 1–2, where a tetrahedrally coordinated FeA atom is replaced by two octahedrally coordinated FeB atoms in the surface layer. This transformation serves as a precursor to the emergence of an FeO-like termination under highly reducing conditions. A key insight from our study is the importance of thoroughly sampling different charge-order configurations to identify the global minima across varying stoichiometries.