Dissolution of iron oxides in water plays a critical role in corrosion, mineral cycling, and surface reactivity; yet, the atomic-scale mechanisms governing Fe release remain poorly understood. Here, we employ ab initio molecular dynamics and well-tempered metadynamics simulations to investigate the stepwise dissolution of surface Fe atoms from the -Fe2O3(0001) surface in aqueous solution. The dissolution process initiates from a stable surface configuration in which Fe is coordinated to three lattice oxygen atoms and one water molecule. It proceeds through a series of metastable states involving additional water coordination, proton-assisted Fe-O bond weakening, and eventual detachment from the substrate. The first major transition, requiring 46.5 kJ/mol, involves breaking the hydrogen-bonding net and overcoming steric hindrance to allow adsorption of a second water molecule. Intermediate barriers (10.9–30.3 kJ/mol) are associated with further coordination and bond cleavage steps. In contrast, the final release of Fe into the solution, corresponding to a state coordinated with four water molecules and no lattice oxygen, exhibits a much higher free-energy barrier of ~ 93.0 kJ/mol. This barrier arises from the formation of a rigid hydrogen-bonded water cage and the loss of proton access to the remaining surface oxygen site, as confirmed by radial distribution function analysis. Our findings reveal why -Fe2O3(0001) is highly resistant to complete dissolution yet prone to surface roughening, defect formation, and adatom structures under aqueous conditions.
Zhou et al. (Sun,) studied this question.