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Corrosion Behavior of FeCrxMnAlCu High-Entropy Alloys in 3.5wt% NaCl Solution
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Affiliation:

1.School of Material Science and Engineering, Lanzhou University of Technology, Lanzhou 730050, China;2.State Key Laboratory of Advanced Processing and Recycling of Nonferrous Metals, Lanzhou University of Technology, Lanzhou 730050, China

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Gansu Provincial Science and Technology Major Special Program (24ZDWA008); Fourth Batch of Top Leading Talents Fund Projects in Gansu Province (ZZ2023G50100013)

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    Abstract:

    In this study, FeCr?MnAlCu (x=0, 0.5, 1.0, 1.5, 2.0) high-entropy alloys were fabricated using vacuum arc melting, and the corrosion behavior of these alloys in 3.5wt% NaCl solution at room temperature was investigated by electrochemical dynamic potential polarization curves and immersion experiments. The microstructure results show that the high-entropy alloy with x=0 has a body-centered cubic phase structure, whereas the high-entropy alloys with x=0.5–2.0 have a mixed face-centered cubic+body-centered cubic dual-phase structure. The corrosion results show that the corrosion resistance of the high-entropy alloy is increased with the increase in Cr content. Among them, the high-entropy alloy with x=2.0 exhibits the optimal corrosion resistance: the highest self-corrosion potential (Ecorr=-0.354 V vs. Ag/AgCl), the smallest self-corrosion current density (Icorr=1.991×10-6 A·cm-2), and the smallest corrosion rate (0.0292 mm/a). The composite passivation film of oxides and hydroxides is formed on the surface of the corroded high-entropy alloys, and the Cr2O3 content is increased with the increase in Cr content, which effectively improves the stability and protective properties of the passivation film.

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[Feng Li, Zhang Xian, Ma Kai, Zhao Yanchun, Ling Yajun, Liu Ruilong, Fu Xuan. Corrosion Behavior of FeCrxMnAlCu High-Entropy Alloys in 3.5wt% NaCl Solution[J]. Rare Metal Materials and Engineering,2026,55(4):877~889.]
DOI:10.12442/j. issn.1002-185X.20250060

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History
  • Received:February 08,2025
  • Revised:March 18,2025
  • Adopted:March 20,2025
  • Online: February 11,2026
  • Published: January 31,2026