MAX phase coatings: synthesis, protective performance, and functional characteristics

Abstract

Mn+1AXn (MAX) phases are a novel class of materials with a closely packed hexagonal structure that bridge the gap between metals and ceramics, garnering tremendous research interest worldwide in recent years. Benefiting from their unique layered structure and mixed covalent–ionic–metallic bonding characteristics, MAX phase coatings possess excellent oxidation resistance, and exceptional electrical and thermal conductivities, making them highly promising for applications in advanced nuclear materials, battery plate protection materials, and aero-engine functional materials. This review aims to provide a comprehensive understanding of MAX phase coatings. It presents an overview of their compositions and microstructure, highlighting well-established structures like 211, 312, and 413. Furthermore, it delves into the various synthesis methods employed in fabricating MAX phase coatings, including physical vapor deposition, chemical vapor deposition, spraying methods, and laser cladding, among others. The potential applications of MAX phase coatings, high-temperature oxidation resistance, mechanical protection, salt spray corrosion resistance, etc., are also investigated. Finally, this review discusses the future potential of MAX phase coatings and proposes areas for further research and improvement. The primary goal is to offer theoretical guidance and innovative ideas for the synthesis and development of superior MAX phase coatings for commercial applications.

Graphical abstract: MAX phase coatings: synthesis, protective performance, and functional characteristics

Article information

Article type
Review Article
Submitted
30 juil. 2024
Accepted
13 déc. 2024
First published
18 déc. 2024

Mater. Horiz., 2025, Advance Article

MAX phase coatings: synthesis, protective performance, and functional characteristics

G. Ma, A. Zhang, Z. Wang, K. Wang, J. Zhang, K. Xu, Y. Xu, S. Zhou and A. Wang, Mater. Horiz., 2025, Advance Article , DOI: 10.1039/D4MH01001A

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