Effects of Chloride Ions on Passive Oxide Films Formed on Cr-Fe-Co-Ni(-Mo) Multi-Principal Element Alloy Surfaces

The composition and stratification of the passive oxide films formed on three Cr-Fe-Co-Ni(-Mo) multi-principal element alloys by electrochemical anodic passivation in sulfuric acid electrolyte containing 0.2 and 4.7 M NaCl were investigated, combining X-ray photoelectron spectroscopy and time-of-flight secondary ion mass spectrometry surface analysis. The passive films show a bilayer structure similar to that formed in Cl--free electrolyte with an inner layer mostly consisting of Cr oxide and an outer layer containing of Cr hydroxide, Ni hydroxide, Mo oxides, and Fe (hydr)oxide. The Mo-free alloy exhibits a thickening of the inner Cr oxide layer and the thinning of the outer layer in 0.2 M Cl-, whereas the two Mo-containing alloys do not show significant alteration even in 4.7 M Cl- evidencing their higher stability in Cl--containing solutions. The chloride penetration is limited to the external part of the outer oxide layer, except in the most severe tested conditions where traces reach the inner barrier layer, and the chloride entry into the layer is strongly reduced after pre-passivation in Cl--free solution. The results allow us to discuss the beneficial effects of pre-passivation in Cl--free conditions and Mo addition providing these alloys enhanced resistance to passivity breakdown.

Automated summary

The composition and stratification of passive oxide films on multi-principal element alloys were investigated using X-ray photoelectron spectroscopy and time-of-flight secondary ion mass spectrometry surface analysis. The results showed that the alloys with Mo exhibit higher stability in Cl--containing solutions compared to the Mo-free alloy. Furthermore, pre-passivation in Cl--free conditions and Mo addition enhance the resistance of these alloys to passivity breakdown.