Abstract

This study investigates the design, microstructure, and performance profile of a novel composite coating combining a high-entropy alloy (HEA) matrix with cermet reinforcement. A 50wt.%CoCrFeMnNi0.8V–50wt.% Cr3C2-Ni80Cr20 powder mixture was successfully deposited onto steel substrates via high-velocity oxy-fuel (HVOF) thermal spraying. Microstructural analysis revealed a highly dense, well-bonded coating architecture (450–500 μm thick) where partially melted, spherical HEA splats were uniformly surrounded by the Cr3C2-Ni80Cr20 phase. X-ray diffraction confirmed a complex multiphase evolution consisting of FCC, BCC, and σ-NiCr phases driven by the rapid solidification inherent to the HVOF process. Tribological evaluations via ball-on-disc testing demonstrated that incorporating the Cr3C2-Ni80Cr20 reinforcement significantly improves wear resistance compared to the monolithic HEA coating. The composite’s wear behavior is governed by a synergistic mechanism: the ductile HEA matrix accommodates plastic deformation, while the harder carbide particles enhance load-bearing capacity, transitioning from adhesive wear to mild third-body abrasion and protective tribo-oxidation. Conversely, electrochemical testing in a 3.5 wt.% NaCl solution showed that the composite coating exhibits higher corrosion current densities (10.53 × 10−6 A/cm2) and more active corrosion potentials than the pure HEA matrix. This behavior is attributed to localized micro-galvanic cells forming at the heterogeneous interfaces between the different phases, alongside chloride-induced destabilization of the surface oxide film. Overall, the novel composite coating offers a compelling, sustainable alternative for surface engineering applications requiring a balanced trade-off between mechanical toughness and acceptable environmental durability. This behavior is also verified by the comparison with previous results dealing with monolithic CoCrFeMnNi0.8V and 75wt.%CoCrFeMnNi0.8V–25wt.% Cr3C2-Ni80Cr20 thermal sprayed coatings, where it is evident that the increase of the reinforcing phase leads to an optimum combination of properties.

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