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In this paper, we study the elastic properties of the entropy-stabilized oxide (Mg, Co, Ni, Cu, Zn)O using experimental and first principles techniques. Our measurements of the indentation modulus on grains with a wide range of crystallographic orientations of the entropy-stabilized oxide revealed a high degree of elastic isotropy at ambient conditions. First principles calculations predict mild elastic anisotropy for the paramagnetic structure, which decreases when the system is considered to be non-magnetic. When the antiferromagnetic state of CoO, CuO, and NiO is accounted for in the calculations, a slight increase in elastic anisotropy is observed, suggesting a coupling between magnetic ordering and the orientation dependent elastic properties. Furthermore, an examination of the local structure reveals that the isotropy is favored through local ionic distortions of Cu and Zn—due to their tendencies to form tenorite and wurtzite phases. The relationships between the elastic properties of the multicomponent oxide and those of its constituent binary oxides are reviewed. These insights open up new avenues for controlling isotropy for technological applications through tuning composition and structure in the entropy-stabilized oxide or the high-entropy compounds in general. [ABSTRACT FROM AUTHOR]

The Ruddlesden–Popper (RP) layered perovskite structure is of great interest due to its inherent tunability, and the emergence and growth of the compositionally complex oxide (CCO) concept endows the RP family with further possibilities. Here, a comprehensive assessment of thermodynamic stabilization, local order/disorder, and lattice distortion was performed in the first two reported examples of lanthanum-deficient Lan+1BnO3n+1 (n = 1, B = Mg, Co, Ni, Cu, Zn) obtained via various processing conditions. Chemical short-range order (CSRO) at the B-site and the controllable excess interstitial oxygen (δ) in RP-CCOs are uncovered by neutron pair distribution function analysis. Reverse Monte Carlo analysis of the data, Metropolis Monte Carlo simulations, and extended x-ray absorption fine structure analysis implies a modest degree of magnetic element segregation on the local scale. Further, ab initio molecular dynamics simulations results obtained from special quasirandom structure disagree with experimentally observed CSRO but confirm Jahn–Teller distortion of CuO6 octahedra. These findings highlight potential opportunities to control local order/disorder and excess interstitial oxygen in layered RP-CCOs and demonstrate a high degree of freedom for tailoring application-specific properties. They also suggest a need for expansion of theoretical and data modeling approaches in order to meet the innate challenges of CCO and related high-entropy phases. [ABSTRACT FROM AUTHOR]

The dependence of the polarization texture topology in ferroelectric PbTiO3 nanoparticles, embedded in a dielectric matrix, on the particle shape and size was investigated with a time-dependent Landau-Ginzburg-Devonshire approach combined with coupled-physics finite-element-method based simulations. Particle shapes belonging to the superellipsoidal family were probed, including octahedral, cubic, and intermediate geometries. For each shape, a parametric sweep of particle sizes ranging from 2 to 40 nm was conducted, revealing a general trend for the texture transformations from a monodomain, through a vortex-like, to a multidomain state, as the size increases. Critical particle sizes for the texture instabilities were found to be strongly dependent on the particle shape, with octahedral particles undergoing transitions at much larger volumes, compared to the cubic particles. Furthermore, for each of the considered non-spherical shapes of appropriate size, it was possible to obtain multiple vortex-like textures whose paraelectric cores are aligned with every rotational axis of the particle point symmetry group. The shape-dependent metastability of the vortex-like textures opens up new avenues for controlling polarization at the nanoscale in a variety of technological applications. [ABSTRACT FROM AUTHOR]

A general approach for fitting Landau-Devonshire thermodynamic potentials directly from first principles is developed for simple displacive ferroelectric perovskite materials. As the first step, a PbTiO3 potential is parameterized completely from density functional theory calculations as a test case, under the only assumption that the transition between the non-polar and polar phases is of first order. The utility of this approach is assessed by comparing quantities characterizing the phase transition, dielectric and piezoelectric properties and equibiaxial strain-temperature phase diagrams with the predictions of several thermodynamic potentials parameterized from experimental data. In the second step, a similar parameterization is generated for a fictitious polar perovskite SnTiO3, enabling us to predictively evaluate an approximate 'equibiaxial strain-temperature-spontaneous polarization' phase diagram for its thin films. [ABSTRACT FROM AUTHOR]

Epitaxial thin films of CuMnAs have recently attracted attention due to their potential to host relativistic antiferromagnetic spintronics and exotic topological physics. Here, we report on the structural and electronic properties of a tetragonal CuMnAs thin film studied using scanning tunneling microscopy (STM) and density functional theory (DFT). STM reveals a surface terminated by As atoms, with the expected semi-metallic behavior. An unexpected zigzag step edge surface reconstruction is observed with emerging electronic states below the Fermi energy. DFT calculations indicate that the step edge reconstruction can be attributed to an As deficiency that results in changes in the density of states of the remaining As atoms at the step edge. This understanding of the surface structure and step edges on the CuMnAs thin film will enable in-depth studies of its topological properties and magnetism. [ABSTRACT FROM AUTHOR]

We report the results of a computational first-principles study of the structural and electrical properties of three ferroelectric diisopropylammonium halides containing chlorine, bromine, and iodine. Calculations were carried out using density-functional theory with maximally-localized Wannier functions utilized for computing electrical polarization within the Modern Theory of Polarization formalism. For each of the crystals, the polar properties for all of the relevant polymorphs were evaluated and decomposed into contributions from individual positive diisopropylammonium and negative halogen-ion charge centers. The calculations show that each diisopropylammonium-halide unit in the crystal possesses a substantial dipole moment with magnitude of 10 to 15 Debye, but that these dipoles are arranged in a mutually opposing manner, leading to full cancellation in the paraelectric phase. In the ferroelectric phase, the dipoles cant along a common polar axis, inducing a small net dipole moment in the crystallographic unit cell, with spontaneous polarization ranging from 5 μC cm−2 for the iodide to 6 μC cm−2 for the bromide and 7 μC cm−2 for the chloride, suggesting no strong dependence of the polarization on the chemical identity of the halide counter ion. We propose that structural modifications of the diisopropylammonium-halide system aimed at stabilization of large unit-dipole cantings could produce molecular crystals with greatly increased spontaneous polarization. [ABSTRACT FROM AUTHOR]

PbTiO3-based ferroelectrics have impressive electroactive properties, originating from the Pb2+ 6s2 electron lone-pair, which cause large elastic distortion and electric polarization due to cooperative pseudo Jahn-Teller effect. Recently, tin-based perovskite oxide (SnTiO3) containing Sn2+ and a chemistry similar to that of the 6s2 lonepair has been identified as a thermally stable, environmentally friendly substitute for PbTiO3-based ferroelectrics. However experimental attempts to stabilize Sn2+ on the A-site of perovskite ATiO3 have so far failed. In this work, we report on the growth of atomically smooth, epitaxial, and coherent Sn-alloyed SrTiO3 films on SrTiO3 (001) substrates using a hybrid molecular beam epitaxy approach. With increasing Sn concentration, the out-of-plane lattice parameter first increases in accordance with the Vegard's law and then decreases for Sn/(Sr+Ti+Sn) at. % ratio > 0.1 due to the incorporation of Sn2+ at the A-site. Using a combination of high-resolution X-ray photoelectron spectroscopy and density functional calculations, we show that while majority of Sn is on the B-site, there is a quantitatively unknown fraction of Sn being consistent with the A-site occupancy making SrTiO3 polar. A relaxor-like ferroelectric local distortion with monoclinic symmetry, induced by A-site Sn2+, was observed in Sn-doped SrTiO3 with Sn/(Sr+Ti+Sn) at. % ratio = 0.1 using optical second harmonic generation measurements. The role of growth kinetics on the stability of Sn2+ in SrTiO3 is discussed. [ABSTRACT FROM AUTHOR]

Using the van der Waals density functional with C09 exchange (vdW-DF-C09), which has been applied to describing a wide range of dispersion-bound systems, we explore the physical properties of prototypical ABO3 bulk ferroelectric oxides. Surprisingly, vdW-DF-C09 provides a superior description of experimental values for lattice constants, polarization and bulk moduli, exhibiting similar accuracy to the modified Perdew-Burke-Erzenhoff functional which was designed specifically for bulk solids (PBEsol). The relative performance of vdW-DF-C09 is strongly linked to the form of the exchange enhancement factor which, like PBEsol, tends to behave like the gradient expansion approximation for small reduced gradients. These results suggest the general-purpose nature of the class of vdW-DF functionals, with particular consequences for predicting material functionality across dense and sparse matter regimes. [ABSTRACT FROM AUTHOR]