No Arabic abstract
The rotation of octahedra (octahedral tilting) is common in ABO3 perovskites and relevant to many physical phenomena, ranging from electronic and magnetic properties, metal-insulator transitions to improper ferroelectricity. Hydrostatic pressure is an efficient way to tune and control octahedral tiltings. However, the pressure behavior of such tiltings can dramatically differ from one material to another, with the origins of such differences remaining controversial. In this work, we discover several new mechanisms and formulate a set of simple rules that allow to understand how pressure affects oxygen octahedral tiltings, via the use and analysis of first-principles results for a variety of compounds. Besides the known A-O interactions, we reveal that the interactions between specific B-ions and oxygen ions contribute to the tilting instability. We explain the previously reported trend that the derivative of the oxygen octahedral tilting with respect to pressure (dR/dP) usually decreases with both the tolerance factor and the ionization state of the A-ion, by illustrating the key role of A-O interactions and their change under pressure. Furthermore, three new mechanisms/rules are discovered. We further predict that the polarization associated with the so-called hybrid improper ferroelectricity could be manipulated by hydrostatic pressure, by indirectly controlling the amplitude of octahedral rotations.
The structure of ABO3 perovskites is dominated by two types of unstable modes, namely, the oxygen octahedral rotation (AFD) and ferroelectric (FE) mode. It is generally believed that such AFD and FE modes tend to compete and suppress each other. Here we use first-principles methods to show that a dual nature of the AFD-FE coupling, which turns from competitive to cooperative as the AFD mode strengthens, occurs in numerous perovskite oxides. We provide a unified model of such a dual interaction by introducing novel high-order coupling terms, and explain the atomistic origin of the resulting new form of ferroelectricity in terms of universal steric mechanisms. We also predict that such a novel form of ferroelectricity leads to atypical behaviors, such as an enhancement of the electric polarization under hydrostatic pressure.
We present a resonant x-ray scattering study of the octahedral tilt order between 50K and 310K in La_7/8Sr_1/8MnO_3. At the La L_II-edge the resonant (300) reflection probes cooperative tilts of the MnO_6-octahedra in this material, as verified by a model caclulation as well as a LDA+U study. The investigation of the octahedral tilts as a function of temperature and the comparison to the lattice parameters, the magnetization and the superlattice reflections related to charge and/or orbital order reveal an intimate coupling between electronic and tilt degrees of freedom in La_7/8Sr_1/8MnO_3.
One-dimensional inorganic nanotubes hold promise for technological applications due to their distinct physical/chemical properties, but so far advancements have been hampered by difficulties in producing single-wall nanotubes with a well-defined radius. In this work we investigate, based on Density Functional Theory (DFT), the formation mechanism of 135 different inorganic nanotubes formed by the intrinsic self-rolling driving force found in asymmetric 2D Janus sheets. We show that for isovalent Janus sheets, the lattice mismatch between inner and outer atomic layers is the driving force behind the nanotube formation, while in the non-isovalent case it is governed by the difference in chemical bond strength of the inner and outer layer leading to steric effects. From our pool of candidate structures we have identified more than 100 tubes with a preferred radius below 35 {AA}, which we hypothesize can display unique properties compared to their parent 2D monolayers. Simple descriptors have been identified to accelerate the discovery of small-radius tubes and a Bayesian regression approach has been implemented to assess the uncertainty in our predictions on the radius.
The structural stability of thermoelectric materials is a subject of growing importance for their energy harvesting applications. Here, we study the microscopic mechanisms governing the structural stability change of zinc antimony at its working temperature, using molecular dynamics combined with experimental measurements of the electrical and thermal conductivity. Our results show that the temperature-dependence of the thermal and electrical transport coefficients is strongly correlated with a structural transition. This is found to be associated with a relaxation process, in which a group of Zn atoms migrates between interstitial sites. This atom migration gradually leads to a stabilizing structural transition of the entire crystal framework, and then results in a more stable crystal structure of $beta-$ Zn4Sb3 at high temperature.
Given the consensus that pressure improves cation order in most of known materials, a discovery of pressure-induced disorder could require reconsideration of order-disorder transition in solid state physics/chemistry and geophysics. Double perovskites Y2CoIrO6 and Y2CoRuO6 synthesized at ambient pressure show B-site order, while the polymorphs synthesized at 6 and 15 GPa are partially-ordered and disordered respectively. With the decrease of ordering degrees, the lattices are shrunken and the crystal structures alter from monoclinic to orthorhombic symmetry. Correspondingly, long-range ferrimagnetic order in the B-site ordered phases are gradually overwhelmed by B-site disorder. Theoretical calculations suggest that unusual unit cell compressions under external pressures unexpectedly stabilize the disordered phases of Y2CoIrO6 and Y2CoRuO6.