Kinetics unveil microstructure development in high-entropy carbide systems, suggesting tailored properties through controlled synthesis.
In this study, medium- and high-entropy carbide systems with compositions WC-TiC-TaC-HfC and WC-TiC-TaC-HfC-ZrC were successfully synthesized via a combination of mechanical activation (using high-energy ball milling, HEBM) and spark plasma sintering (SPS) at 1900 °C. Investigation of the SPS consolidation kinetics revealed that both systems undergo single-stage active densification via a solid-state sintering mechanism within the temperature range of 1316–1825 °C. The introduction of ZrC into the five-component system led to a 22% decrease in the maximum shrinkage rate (from 0.9 to 0.7 mm·min−1), which is attributed to the manifestation of a sluggish diffusion effect, characteristic of high-entropy systems. X-ray diffraction analysis of the consolidated samples confirmed the formation of predominantly single-phase high-entropy solid solutions (W-Ti-Ta-Hf)C and (W-Ti-Ta-Hf-Zr)C with a NaCl-type cubic structure (space group Fm-3m) and lattice parameters of 4.4101 Å and 4.4604 Å, respectively. Energy-dispersive X-ray spectroscopy revealed a near-equimolar distribution of metallic components with deviations not exceeding ±1.9 at. %. The addition of ZrC increased the average crystallite size by 84.3% (from 83.6 to 153.1 nm). Both systems achieved comparable relative densities of ~91.75%; however, they exhibited differences in hardness distribution: the four-component system is characterized by a higher average microhardness (1860 HV), while the five-component system exhibits a higher macrohardness HV30 (2008.1). The established correlations between composition, phase formation, microstructure, and properties provide a fundamental basis for the targeted design of high-entropy carbide ceramics with tailored characteristics for high-temperature applications.
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Buravlev et al. (2025) studied this question.
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