No Arabic abstract
Using classical Monte Carlo simulations, we study a simple statistical mechanical model of relevance to the emergence of polarisation from local displacements on the square and cubic lattices. Our model contains two key ingredients: a Kitaev-like orientation-dependent interaction between nearest neighbours, and a steric term that acts between next-nearest neighbours. Taken by themselves, each of these two ingredients is incapable of driving long-range symmetry breaking, despite the presence of a broad feature in the corresponding heat capacity functions. Instead each component results in a hidden transition on cooling to a manifold of degenerate states, the two manifolds are different in the sense that they reflect distinct types of local order. Remarkably, their intersection---emph{i.e.} the ground state when both interaction terms are included in the Hamiltonian---supports a spontaneous polarisation. In this way, our study demonstrates how local ordering mechanisms might be combined to break global inversion symmetry in a manner conceptually similar to that operating in the hybrid improper ferroelectrics. We discuss the relevance of our analysis to the emergence of spontaneous polarisation in well-studied ferroelectrics such as BaTiO$_3$ and KNbO$_3$.
Dabconium hybrid perovskites include a number of recently-discovered ferroelectric phases with large spontaneous polarisations. The origin of ferroelectric response has been rationalised in general terms in the context of hydrogen bonding, covalency, and strain coupling. Here we use a combination of simple theory, Monte Carlo simulations, and density functional theory calculations to assess the ability of these microscopic ingredients---together with the always-present through-space dipolar coupling---to account for the emergence of polarisation in these particular systems whilst not in other hybrid perovskites. Our key result is that the combination of A-site polarity, preferred orientation along $langle111rangle$ directions, and ferroelastic strain coupling drives precisely the ferroelectric transition observed experimentally. We rationalise the absence of polarisation in many hybrid perovskites, and arrive at a set of design rules for generating FE examples beyond the dabconium family alone.
Our detailed temperature dependent synchrotron powder x-ray diffraction studies along with first-principles density functional perturbation theory calculations, enable us to shed light on the origin of ferroelectricity in GdCrO3. The actual lattice symmetry is found to be noncentrosymmetric orthorhombic Pna21 structure, sup- porting polar nature of the system. Polar distortion is driven by local symmetry breaking and by local distortions dominated by Gd off-centering. Our study reveals an intimate analogy between GdCrO3 and YCrO3. However, a distinctive difference exists that Gd is less displacive compared to Y, which results in an orthorhombic P na21 structure in GdCrO3 in contrast to monoclinic structure in YCrO3 and consequently, decreases its polar property. This is due to the subtle forces involving Gd-4f electrons either directly or indirectly. A strong magneto-electric coupling is revealed using Raman measurements based analysis in the system below Cr-ordering temperature, indicating their relevance to ferroelectric modulation.
We show that compounds in a family that possess time-reversal symmetry and share a non-centrosymmetric cubic structure with the space group F-43m (No. 216) host robust ideal Weyl semi-metal fermions with desirable topologically protected features. The candidates in this family are compounds with different chemical formulas AB2, ABC, ABC2, and ABCD and their Fermi levels are predominantly populated by nontrivial Weyl fermions. Symmetry of the system requires that the Weyl nodes with opposite chirality are well separated in momentum space. Adjacent Weyl points have the same chirality, thus these Weyl nodes would not annihilate each other with respect to lattice perturbations. As Fermi arcs and surface states connect Weyl nodes with opposite chirality, the large separation of the latter in momentum space guarantees the appearance of very long arcs and surface states. This work demonstrates the use of system symmetry by first-principles calculations as a powerful recipe for discovering new Weyl semi-metals with attractive features whose protected fermions may be candidates of many applications.
Whereas low-temperature ferroelectrics have a well understood ordered spatial dipole arrangement, the fate of these dipoles in paraelectric phases remains poorly understood. This is studied here as an energy minimization problem using both static and molecular dynamic (MD) density functional theory (DFT). We find that considering the non-thermal internal energy already reveals the formation of a distribution of static local displacements that (i) mimic the symmetries of the low temperature phases, while (ii) being the precursors of what high temperature DFT MD finds as thermal motifs.
In a one-dimensional (1D) system with degenerate ground states, their domain boundaries, dubbed solitons, emerge as topological excitations often carrying unconventional charges and spins; however, the soliton excitations are only vital in the non-ordered 1D regime. Then a question arises; how do the solitons conform to a 3D ordered state? Here, using a quasi-1D organic ferroelectric, TTF-CA, with degenerate polar dimers, we pursue the fate of a spin-soliton charge-soliton composite matter in a 1D polar-dimer liquid upon its transition to a 3D ferroelectric order by resistivity, NMR and NQR measurements. We demonstrate that the soliton matter undergoes neutral spin-spin soliton pairing and spin-charge soliton pairing to form polarons, coping with the 3D order. The former contributes to the magnetism through triplet excitations whereas the latter carries electrical current. Our results reveal the whole picture of a soliton matter that condenses into the 3D ordered state.