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The difficult synthesis and low purity of 413 high-entropy MAX phase powders have severely constrained their development in the field of electromagnetic wave absorption. To address this, the present study optimized a two-step solid-phase synthesis process. By examining how different raw-material pretreatment methods affect the structural evolution of carbide precursors, we proposed a “structural genetic mechanism” that systematically explains the synthesis pathway of the 413 high-entropy MAX phase. The results show that cubic-phase carbide precursors are essential for producing 413 high-purity high-entropy MAX. Using the optimized method, we synthesized pure-phase 413 high-entropy MAX and, for the first time, successfully prepared (Mo0.2Ta0.2Nb0.2Ti0.2V0.2)4AlC3 via a conventional pressureless solid-state reaction route. Wave absorption tests indicate that the synthesized 413 high-entropy MAX phases all exhibit good absorption performance. In particular, (Mo0.2Cr0.2Nb0.2Ti0.2V0.2)4AlC3 achieved a maximum effective absorption bandwidth (EABmax) of 4.24 GHz at a thickness of 1.57 mm and a minimum reflection loss (RLmin) of −52.88 dB at 1.87 mm. (Mo0.2Ta0.2Nb0.2Ti0.2V0.2)4AlC3 showed a clear advantage at small thicknesses, with an EABmax of 3.44 GHz at 0.93 mm and an RLmin of −51.60 dB at 0.89 mm. This study fully demonstrated the effective regulation of wave absorption performance by high-entropy engineering and provided an effective approach to expand the types of 413 high-entropy MAX phase powders, offering a useful reference for exploring this material in the field of wave absorption.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, http://creativecommons.org/licenses/by/4.0/).
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