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The high-entropy concept was applied to synthesize a set of rare-earth perovskites REBO3 (RE = La, Pr, Nd, Sm, Eu, Gd) with the B-site occupied by Sc, Al, Cr, Ni, and Fe in equimolar ratios. All samples crystallize in the orthorhombic Pnma space group. Using an extended set of characterization measurements, the effects of multi-component material design and rare-earth selection on the electronic properties are explored. Transport measurements show semiconducting behavior. PrBO3, SmBO3, and LaBO3 show low-temperature magnetic ordering, with the ordering temperature shifting with the moment on the A-site. 

Abstract The mechanical behavior and microstructural evolution of a BCC‐phase NbTaTiV refractory multi‐principal element alloy (RMPEA) is studied over a wide range of strain rates (10⁻³to 10³s⁻¹) and temperatures (room temperature to 850 °C). The mechanical property of present RMPEA shows less strain‐rate dependence and strong resistance to softening at high temperatures. Under high strain‐rate loading, the formation of thin type‐I twins is observed, which could lead to an increase in strain‐hardening rates. However, this hardening mechanism competes with adiabatic heating effects, resulting in the deterrence of strain‐hardening behaviors. In contrast, substantial strain‐hardening occurs at cryogenic temperatures due to the formation of twins, which act as stronger barriers to dislocation motion and interact with each other. To further understand the different strain‐hardening behaviors, density functional theory (DFT) calculations predict relatively low stacking fault energies and high twinning stress for the NbTaTiV RMPEA. 

The coupling between ferroelectric and magnetic order provides a powerful means to control magnetic properties with electric fields. In this study, we have investigated the magnetoelectric (ME) coupling in iridate-oxide based superlattices employing first-principles density functional theory (DFT) calculations. In particular, we have investigated several oxide superlattices, including (SrIrO 3 ) 1 –(CaTiO 3 ) 1 (SIO–CTO) and (SrIrO 3 ) 1 –(BaTiO 3 ) 1 (SIO–BTO), with an alternating single layer of SIO and CTO/BTO. We identify a very large ME coupling in SIO–BTO mediated by both lattice and electronic contributions. In comparison, moderate ME coupling constants are found in SIO–CTO. Further electronic and structural analyses reveal that the large ME coupling of SIO–BTO is caused by the large spin–orbit coupling of 5d iridium as well as the significant polarization induced in the SIO–BTO. Interestingly, we find that the ME coupling in SIO–BTO can further be enhanced by modulating epitaxial strain. These results suggest a route to significantly enhance the ME coupling effects, which might be applicable for other materials and practical applications.