Thermodynamic feasibility of the four-stage chloride-induced depassivation mechanism of iron
Qin Pang, H. DorMohammadi, O. Burkan Isgor, Líney Árnadóttir
Abstract
Abstract The atomistic mechanism of chloride-induced depassivation of iron is still debated. A recent study suggests a four-stage depassivation mechanism, in general agreement with the point defect model. The proposed four-stage mechanism is based on reactive force field molecular dynamics simulations and is rather complex but here we use density functional theory to confirm the thermodynamic feasibility of the proposed mechanism. We find that the four surface species, formed in the four stages, have decreasing surface stability, which is consistent with the order of species formed in the depassivation process proposed in the reactive force field molecular dynamics study. The Fe vacancy formation energy, that is the energy needed to form a surface Fe vacancy by removing different surface species, indicates that surface species with more chlorides dissolve more easily from the surface, suggesting that chloride acts as catalyst in the iron dissolution process. The results are consistent with the suggested four-stage reaction mechanism and the point defect model.