Abstract
Seven equimolar, five-component, metal diborides were fabricated via high-energy ball milling and spark plasma sintering. Six of them, including (Hf0.2Zr0.2Ta0.2Nb0.2Ti0.2)B2, (Hf0.2Zr0.2Ta0.2Mo0.2Ti0.2)B2, (Hf0.2Zr0.2Mo0.2Nb0.2Ti0.2)B2, (Hf0.2Mo0.2Ta0.2Nb0.2Ti0.2)B2, (Mo0.2Zr0.2Ta0.2Nb0.2Ti0.2)B2, and (Hf0.2Zr0.2Ta0.2Cr0.2Ti0.2)B2, possess virtually one solid-solution boride phase of the hexagonal AlB2 structure. Revised Hume-Rothery size-difference factors are used to rationalize the formation of high-entropy solid solutions in these metal diborides. Greater than 92% of the theoretical densities have been generally achieved with largely uniform compositions from nanoscale to microscale. Aberration-corrected scanning transmission electron microscopy (AC STEM), with high-angle annular dark-field and annular bright-field (HAADF and ABF) imaging and nanoscale compositional mapping, has been conducted to confirm the formation of 2-D high-entropy metal layers, separated by rigid 2-D boron nets, without any detectable layered segregation along the c-axis. These materials represent a new type of ultra-high temperature ceramics (UHTCs) as well as a new class of high-entropy materials, which not only exemplify the first high-entropy non-oxide ceramics (borides) fabricated but also possess a unique non-cubic (hexagonal) and layered (quasi-2D) high-entropy crystal structure that markedly differs from all those reported in prior studies. Initial property assessments show that both the hardness and the oxidation resistance of these high-entropy metal diborides are generally higher/better than the average performances of five individual metal diborides made by identical fabrication processing.
Highlights
Seven equimolar, five-component, metal diborides were fabricated via high-energy ball milling and spark plasma sintering
This work has greatly extended the knowledge of high-entropy materials, since it is the first time crystalline high-entropy non-oxide ceramics have been synthesized, and because these high-entropy metal diborides exhibit a unique layered hexagonal crystal structure with alternating rigid two-dimensional (2D) boron nets and high-entropy 2D layers of metal cations, as schematically shown in Fig. 1, which distinctly differs from any other high-entropy crystalline phases reported to date
To synthesize high-entropy metal diborides, five commercial metal diboride powders of equimolar amounts were mixed and mechanically alloyed via high energy ball milling (HEBM) for six hours; subsequently, the HEBM powders were compacted into disks of 20-mm diameter and densified utilizing spark plasmas sintering (SPS) at 2000 °C for 5 minutes under a pressure of 30 MPa
Summary
Five-component, metal diborides were fabricated via high-energy ball milling and spark plasma sintering. Aberrationcorrected scanning transmission electron microscopy (AC STEM), with high-angle annular dark-field and annular bright-field (HAADF and ABF) imaging and nanoscale compositional mapping, has been conducted to confirm the formation of 2-D high-entropy metal layers, separated by rigid 2-D boron nets, without any detectable layered segregation along the c-axis These materials represent a new type of ultra-high temperature ceramics (UHTCs) as well as a new class of high-entropy materials, which exemplify the first high-entropy non-oxide ceramics (borides) fabricated and possess a unique non-cubic (hexagonal) and layered (quasi-2D) high-entropy crystal structure that markedly differs from all those reported in prior studies. This work has greatly extended the knowledge of high-entropy materials, since it is the first time crystalline high-entropy non-oxide ceramics ( borides) have been synthesized, and because these high-entropy metal diborides exhibit a unique layered hexagonal crystal structure with alternating rigid two-dimensional (2D) boron nets and high-entropy 2D layers of metal cations (as essentially a class of quasi-2D high-entropy materials), as schematically shown in Fig. 1, which distinctly differs from any other high-entropy crystalline phases reported to date
Sign-in/Register to view highlights & summary Sign-in/Register to access full text options 
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
