Abstract

The corrosion behavior of NiCoCu nanocrystalline coatings in neutral salt environments was systematically investigated by potentiodynamic polarization, linear polarization, electrochemical impedance spectroscopy, and long-term salt spray tests. The electrodeposited ternary coatings were Ni-based solid solution alloys that contained markedly different contents of Co and Cu. Greater Co and Cu contents strongly reduced the polarization and charge-transfer resistance of the coatings, thus decreasing their corrosion resistance in neutral NaCl solutions. In salt spray tests, the initial porous corrosion product film on the Co-/Cu-poor coating evolved into a compact film that finally grew to cover the coating surface, while such morphological transition was absent on the Co-/Cu-rich coating, where the formed film showed a continuous deterioration in its initial porous structure. Abundant Co-/Cu-substituted α-Ni(OH)2 might grow to form the primary compact films that could coalesce and thicken as corrosion was suppressed. A large amount of Cu(OH)2 together with high corrosion rates might be detrimental to the formation of compact films. A mechanism of the formation of the corrosion product films was proposed based on the corrosion characteristics of the ternary system and detailed corrosion product film analysis.

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