Magnetite nanoparticles (MNPs) play an important role in geological and environmental systems because of their redox reactivity and ability to sequester a wide range of metals and metalloids. X-ray absorption spectroscopy conducted at metal and metalloid edges has suggested that the magnetite {111} faces of octahedrally shaped nanoparticles play a dominant role in the redox and sorption processes of these elements. However, studies directly probing the magnetite surfaces, especially in their fully solvated state, are scarce. Therefore, we investigated the speciation and stability over a wide Eh/pH range of octahedrally shaped MNPs of 2 nm size by means of Kohn-Sham density functional theory with Hubbard correction (DFT+U). By altering the protonation state of the crystals, a redox-sensitive response of the octahedrally coordinated Fe could be achieved. Furthermore, the preferential H distribution could be identified, highlighting the difference between the edges, vertices, and facets of the nanocrystals. Subsequently, the interactions of the MNPs with a solvent of pure water or a 0.5 M NaCl solution were studied by classical molecular dynamics (MD) simulations. Finally, a comparison of the corresponding macroscopic magnetite (111) surface to the investigated MNPs was conducted.
Keywords: interaction with NaCl; interaction with water; magnetite; magnetite nanoparticles; oxidation/reduction; {111} facet.