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High-entropy alloys (HEAs) are a class of multi-element materials that exhibit unique structural and functional properties. This study reports on the synthesis and characterization of a superconducting HEA, (NbTa)0.55(HfTiZr)0.45 fabricated using the vacuum arc melting technique. Scanning electron microscopy and energy-dispersive x-ray spectroscopy were employed to analyze the material's morphology and composition. X-ray diffraction analysis revealed a single-phase body-centered cubic (BCC) structure with a measured nanoindentation hardness of 6.4 GPa and Young's modulus of 132 GPa. This HEA superconductor was investigated by x-ray diffraction at Beamline 13BM-C, Advanced Photon Source, and the BCC phase was stable to the highest pressure of 50 GPa. Superconductivity was characterized by four-probe resistivity measurements in a quantum design physical property measurement system, yielding a superconducting transition temperature (Tc) of 7.2 K at ambient pressure and reaching a maximum of 10.1 K at the highest applied pressure of 23.6 GPa. The combination of high structural stability enhanced superconducting performance under pressure and superior mechanical properties highlights (NbTa)0.55(HfTiZr)0.45 as a promising superconductor under extreme environments. 

We have studied magnetic ordering in polycrystalline erbium at high pressures up to 32 GPa and low temperatures down to 10 K using neutron diffraction techniques at the Spallation Neutron Source at Oak Ridge National Laboratory, USA. For the hexagonal close-packed (hcp) phase, strong nuclear and magnetic satellite intensities permit a simultaneous refinement of the nuclear and magnetic structures. At 1 GPa of applied pressure, a modulation vector q=γc^* with γ≈2/7 for the c-axis modulated and cycloidal phases is consistent with prior single-crystal studies at low pressures. At 6.7 GPa in the hcp phase, we find γ≈0.31, indicating a reduction in the period of the magnetic structure with respect to the crystal lattice. The magnetic ordering temperature at 6.7 GPa is slightly above 60 K. At 32 GPa in the double hexagonal close-packed phase, the magnetic scattering constrains the magnetic ordering temperature to 25±5 K. Our neutron diffraction study demonstrates that the magnetic ordering persists in the high-pressure double hexagonal close-packed phase of erbium to the highest pressure of 32 GPa. 

A boron-rich boron–carbide material (B4+δC) was synthesized by spark plasma sintering of a ball-milled mixture of high-purity boron powder and graphitic carbon at a pressure of 7 MPa and a temperature of 1930 °C. This high-pressure, high-temperature synthesized material was recovered and characterized by X-ray diffraction, X-ray photoelectron spectroscopy, Raman spectroscopy, Vickers hardness measurements, and thermal oxidation studies. The X-ray diffraction studies revealed a single-phase rhombohedral structure (space group R-3m) with lattice parameters in hexagonal representation as a = 5.609 ± 0.007 Å and c = 12.082 ± 0.02 Å. The experimental lattice parameters result in a value of δ = 0.55, or the composition of the synthesized compound as B4.55C. The high-resolution scans of boron binding energy reveal the existence of a B-C bond at 188.5 eV. Raman spectroscopy reveals the existence of a 386 cm−1 vibrational mode representative of C-B-B linear chain formation due to excess boron in the lattice. The measured Vickers microhardness at a load of 200 gf shows a high hardness value of 33.8 ± 2.3 GPa. Thermal gravimetric studies on B4.55C were conducted at a temperature of 1300 °C in a compressed dry air environment, and its behavior is compared to other high-temperature ceramic materials such as high-entropy transition metal boride. The high neutron absorption cross section, high melting point, high mechanical strength, and thermal oxidation resistance make this material ideal for applications in extreme environments. 

Polydopamine-based bioinspired surface coating can augment improved adhesive nature and functional performance to materials. Here in, we report for the first time the capability of low-temperature hydrogen plasma treatment to enhance the polydopamine coating on 3D-Printed Polymer Scaffolds. The hydrogen plasma-treated scaffolds were systematically characterized with different analytical techniques. It was seen that hydrogen plasma treatment can significantly enhance the polydopamine coating on scaffolds. This observed finding of the utility of plasma to enhance the polydopa- mine coating on 3D-printed polymer scaffolds could significantly reduce the current processing time of polydopamine coating on material surfaces.