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Corrosion-inhibited wear in Fe-based amorphous alloy coatings: Role of antagonistic interactions and rapid repassivation in chloride media

  • Xinlong Zhang
  • , Qiang Li*
  • , Chengwu Zhang
  • , Lei Xie
  • , Guan Zhang
  • , Jie Yin
  • , Yongjiang Huang
  • *Corresponding author for this work
  • Xinjiang University
  • Xinjiang Key Laboratory of Advanced Metallic Materials Design and Application
  • Xinjiang Institute of Engineering
  • Yili Normal University
  • Ltd.
  • Harbin Institute of Technology

Research output: Contribution to journalArticlepeer-review

Abstract

The coupled electrochemical-mechanical degradation of a high-velocity oxygen-fuel (HVOF) sprayed Fe57Cr15Mo8P10C7B3 amorphous alloy coating (AAC) was systematically investigated in a 3.5 wt% NaCl solution and benchmarked against 316 L stainless steel (316 L SS). By coupling in-situ electrochemical techniques with wear-track topometry and X-ray photoelectron spectroscopy (XPS) depth profiling, the fundamental mechanisms governing dynamic wear–corrosion interactions were elucidated. Notably, despite exhibiting a higher static corrosion rate than the 316 L SS, the AAC demonstrated a localized antagonistic contribution to wear-corrosion interaction during sliding. Specifically, the electrochemically driven passivation process actively suppressed mechanical attrition, yielding a negative corrosion-accelerated wear volume (ΔWfc = - (2.75 ± 0.91) × 10−3 mm3). Conversely, the 316 L SS suffered from severe positive synergy (ΔWfc= + (2.22 ± 0.47) × 10−3 mm3), resulting in a nearly threefold higher total material loss. In-situ tribo-electrochemical analyses revealed that the homogeneous amorphous structure of the AAC facilitates ultra-fast repassivation kinetics (trep = 4.4 s, vs. 15.4 s for the 316 L SS), dynamically sustaining a highly stable duplex passive film. XPS profiling further corroborated that this rapidly regenerated tribofilm is significantly thicker (10.55 nm vs. 7.84 nm) and strongly enriched in gel-like FeOOH and protective Mo oxides. Under continuous sliding contact, these tribochemically generated species are proposed to contribute to the formation of a shear-accommodating solid boundary layer, which may reduce direct asperity contact and mitigate abrasive damage. This study provides fundamental insights into the "corrosion-inhibited wear" mechanism of Fe-based AACs, demonstrating that the synergistic coupling of rapid self-healing kinetics and tailored tribofilm chemistry is a highly effective design principle for robust marine tribological applications.

Original languageEnglish
Article number112264
JournalTribology International
Volume223
DOIs
StatePublished - Nov 2026
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 14 - Life Below Water
    SDG 14 Life Below Water

Keywords

  • Corrosion-inhibited wear
  • Fe-based amorphous alloy coating
  • Repassivation kinetics
  • Tribocorrosion

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