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Register a new userSynthesis of superfine high-entropy metal diboride powders
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High-purity and superfine high-entropy metal diboride powders, namely (Hf0.2Zr0.2Ta0.2Nb0.2Ti0.2)B2, were successfully synthesized via a facile borothermal reduction method at 1973 K for the first time. The as-synthesized powders with an average particle size of ~ 310 nm had a single-crystalline hexagonal structure of metal diborides and simultaneously possessed high compositional uniformity from nanoscale to microscale. In addition, their formation mechanisms were well interpreted by analyzing the thermodynamics of the possible chemical reactions based on the first principles calculations. This work will open up a new research field on the synthesis of high-entropy metal diboride powders.
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High-entropy nanomaterials have been arousing considerable interest in recent years due to their huge composition space, unique microstructure, and adjustable properties. Previous studies focused mainly on high-entropy nanoparticles, while other high-entropy nanomaterials were rarely reported. Herein, we reported a new class of high-entropy nanomaterials, namely (Ta0.2Nb0.2Ti0.2W02Mo0.2)B2 high-entropy diboride (HEB-1) nanoflowers, for the first time. The formation possibility of HEB-1 was first theoretically analyzed from two aspects of lattice size difference and chemical reaction thermodynamics. We then successfully synthesized HEB-1 nanoflowers by a facile molten salt synthesis method at 1473 K. The as-synthesized HEB-1 nanoflowers showed an interesting chrysanthemum-like morphology assembled from numerous well-aligned nanorods with the diameters of 20-30 nm and lengths of 100-200 nm. Meanwhile, these nanorods possessed a single-crystalline hexagonal structure of metal diborides and highly compositional uniformity from nanoscale to microscale. In addition, the formation of the as-synthesized HEB-1 nanoflowers could be well interpreted by a classical surface-controlled crystal growth theory. This work not only enriches the categories of high-entropy nanomaterials but also opens up a new research field on the high-entropy diboride nanomaterials.
High-entropy materials have attracted considerable interest due to the combination of useful properties and promising applications. Predicting their formation remains the major hindrance to the discovery of new systems. Here we propose a descriptor - entropy forming ability - for addressing synthesizability from first principles. The formalism, based on the energy distribution spectrum of randomized calculations, captures the accessibility of equally-sampled states near the ground state and quantifies configurational disorder capable of stabilizing high-entropy homogeneous phases. The methodology is applied to disordered refractory 5-metal carbides - promising candidates for high-hardness applications. The descriptor correctly predicts the ease with which compositions can be experimentally synthesized as rock-salt high-entropy homogeneous phases, validating the ansatz, and in some cases, going beyond intuition. Several of these materials exhibit hardness up to 50% higher than rule of mixtures estimations. The entropy descriptor method has the potential to accelerate the search for high-entropy systems by rationally combining first principles with experimental synthesis and characterization.
High-entropy alloys, near-equiatomic solid solutions of five or more elements, represent a new strategy for the design of materials with properties superior to those of conventional alloys. However, their phase space remains constrained, with transition metal high-entropy alloys exhibiting only face- or body-centered cubic structures. Here, we report the high-pressure synthesis of a hexagonal close-packed phase of the prototypical high-entropy alloy CrMnFeCoNi. This martensitic transformation begins at 14 GPa and is attributed to suppression of the local magnetic moments, destabilizing the initial fcc structure. Similar to fcc-to-hcp transformations in Al and the noble gases, the transformation is sluggish, occurring over a range of >40 GPa. However, the behaviour of CrMnFeCoNi is unique in that the hcp phase is retained following decompression to ambient pressure, yielding metastable fcc-hcp mixtures. This demonstrates a means of tuning the structures and properties of high-entropy alloys in a manner not achievable by conventional processing techniques.
Flash sintering phenomena are predominantly associated with ceramics due to thermal runaway of their electric conductivity noticeably represented in materials such as zirconia or silicon carbide. Because of their high electric conductivity, flash sintering of metals is nearly inexistent. In this work, an original metal powder flash sintering method based on a microwave approach is presented. Within the developed approach, an unusually fast (60 s) thermal and sintering runaway of Ti-6Al-4V powder is experimentally revealed under microwave illumination. This phenomenon is simulated based on an electromagnetic-thermal-mechanical (EMTM) model. The developed multiphysics model reveals that the metal powder specimens runaway does not result from its intrinsic material properties, but results from the resonance phenomenon thermally activated by the surrounding tooling material. The EMTM simulation predicts with a very good accuracy the microwave repartition and the resulting densification and powder specimens shape distortions observed experimentally. The comparison of the microwave and conventional sintering kinetics indicates an important acceleration of the sintering behavior under microwave heating. The developed sintering approach has a potential of the implementation for time-effective mass production of small metal parts.
In this work we report a study of the magnetic behavior of ferrimagnetic oxide CoFe2O4 treated by mechanical milling with different grinding balls. The cobalt ferrite nanoparticles were prepared using a simple hydrothermal method and annealed at 500oC. The non-milled sample presented coercivity of about 1.9 kOe, saturation magnetization of 69.5 emu/g, and a remanence ratio of 0.42. After milling, two samples attained coercivity of 4.2 and 4.1 kOe, and saturation magnetization of 67.0 and 71.4 emu/g respectively. The remanence ratio MR/MS for these samples increase to 0.49 and 0.51, respectively. To investigate the influence of the microstructure on the magnetic behavior of these samples, we used X-ray powder diffraction (XPD), transmission electron microscopy (TEM), and vibrating sample magnetometry (VSM). The XPD analysis by the Williamson-Hall plot was used to estimate the average crystallite size and strain induced by mechanical milling in the samples.
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