Abstract
The electrochemical behavior of a bulk-synthesized MgZn2 intermetallic compound in aerated 0.1 M NaCl solutions has been studied as a function of pH and applied potential using polarization techniques, electrochemical impedance spectroscopy (EIS), X-ray photoelectron spectroscopy (XPS), and focused ion beam-transmission electron microscopy (FIB-TEM). The anodic activity of MgZn2 is seen to decrease with an increase in pH value. Polarization tests reveal two limiting current densities in pH 4 solution at relatively high and low potentials. At pH 12, passivity is observed with a lower limiting current density compared to those observed at pH 4. The corrosion film formed after potentiostatic polarization in the pH 4 solution is composed of a bilayer at a less negative potential and a single layer at a more negative potential. In the case of pH 12 solution, a protective compact bilayer film is formed irrespective of the potential within the passive zone. Overall, the corrosion mechanism of MgZn2 is by early dissolution of Mg leading to a Zn-enriched surface whose subsequent dissolution depends on the value of the applied potential.
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This work was financially supported by the National Natural Science Foundation of China (Grant No. 51571201).
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Ikeuba, A.I., Kou, F., Duan, H. et al. Understanding the electrochemical behavior of bulk-synthesized MgZn2 intermetallic compound in aqueous NaCl solutions as a function of pH. J Solid State Electrochem 23, 1165–1177 (2019). https://doi.org/10.1007/s10008-019-04210-y
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DOI: https://doi.org/10.1007/s10008-019-04210-y