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تسجيل مستخدم جديدPrediction of a native ferroelectric metal
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The possibility that metals may support ferroelectricity is an open issue. Anderson and Blount showed that certain martensitic transitions involve inversion symmetry breaking and the formal existence of a polar axis, so metallic ferroelectric behavior has been claimed for metals undergoing a centrosymmetric (CS) to non-CS structural transformation (Cd2ReO7, LiOsO3) or natively non-CS (SrCaRu2O), or for ferroelectric insulators whose polar distortion survives moderate metallicity induced by doping or proximity. However, none of these systems, nor any other to our knowledge, embodies a truly ferroelectric metal with native switchable polarization and native metallicity coexisting in a single phase. Here we report the first-ever theoretical prediction of such a material. By first-principles calculations, we show that the layered perovskite Bi5Ti5O17 has a non-zero density of states at the Fermi level and metal-like conductivity, as well as a spontaneous polarization in zero field. Further, we predict that the polarization of Bi5Ti5O17 is switchable both in principle, as the material complies with the sufficient symmetry requirements, and in practice, as Bi5Ti5O17 can sustain a sizable potential drop along the polar direction, as needed to revert its polarization by application of an electric bias.
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Metals cannot exhibit ferroelectricity because static internal electric fields are screened by conduction electrons, but in 1965, Anderson and Blount predicted the possibility of a ferroelectric metal, in which a ferroelectric-like structural transit
ion occurs in the metallic state. Up to now, no clear example of such a material has been identified. Here we report on a centrosymmetric (R-3c) to non-centrosymmetric (R3c) transition in metallic LiOsO3 that is structurally equivalent to the ferroelectric transition of LiNbO3. The transition involves a continuous shift in the mean position of Li+ ions on cooling below 140K. Its discovery realizes the scenario described by Anderson and Blount, and establishes a new class of materials whose properties may differ from those of normal metals.
Materials with reduced dimensions have been shown to host a wide variety of exotic properties and novel quantum states that often defy textbook wisdom1-5. Ferroelectric polarization and metallicity are well-known examples of mutually exclusive proper
ties that cannot coexist in bulk solids because the net electric field in a metal can be fully screened by free electrons6. An atomically thin metallic layer capped by insulating layers has shown decent conductivity at room temperature7. Moreover, a penetrating polarization field can be employed to induce an ion displacement and create an intrinsic polarization in the metallic layer. Here we demonstrate that a ferroelectric metal can be artificially synthesized through imposing a strong polarization field in the form of ferroelectric/unit-cell-thin metal superlattices. In this way the symmetry of an atomically thin conductive layer can be broken and manipulated by a neighboring polar field, thereby forming a two-dimensional (2D) ferroelectric metal. The fabricated of (SrRuO3)1/(BaTiO3)10 superlattices exhibit ferroelectric polarization in an atomically thin layer with metallic conductivity at room temperature. A multipronged investigation combining structural analyses, electrical measurements, and first-principles electronic structure calculations unravels the coexistence of 2D electrical conductivity in the SrRuO3 monolayer accompanied by the electric polarization. Such 2D ferroelectric metal paves a novel way to engineer a quantum multi-state with unusual coexisting properties, such as ferroelectrics, ferromagnetics and metals, manipulated by external fields8,9.
Ferroelectric materials contain a switchable spontaneous polarization that persists even in the absence of an external electric field. The coexistence of ferroelectricity and metallicity in a material appears to be illusive, since polarization is ill
-defined in metals, where the itinerant electrons are expected to screen the long-range dipole interactions necessary for dipole ordering. The surprising discovery of the polar metal, LiOsO3 has generated interest in searching for new polar metals motivated by the prospects of exotic quantum phenomena such as unconventional pairing mechanisms giving rise to superconductivity, topological spin currents, anisotropic upper critical fields, and Mott multiferroics. Previous studies have suggested that the coordination preferences of the Li atom play a key role in stabilizing the polar metal phase of LiOsO3, but a thorough understanding of how polar order and metallicity can coexist remains elusive. Here, we use XUV-SHG as novel technique to directly probe the broken inversion-symmetry around the Li atom. Our results agree with previous theories that the primary structural distortion that gives rise to the polar metal phase in LiOsO3 is a consequence of a sub-Angstrom Li atom displacement along the polar axis. A remarkable agreement between our experimental results and ab initio calculations provide physical insights for connecting the nonlinear response to unit-cell spatial asymmetries. It is shown that XUV-SHG can selectively probe inversion-breaking symmetry in a bulk material with elemental specificity. Compared to optical SHG methods, XUV-SHG fills a key gap for studying structural asymmetries when the structural distortion is energetically separated from the Fermi surface. Further, these results pave the way for time-resolved probing of symmetry-breaking structural phase transitions on femtosecond timescales with element specificity.
We propose a ferromagnetic Heusler alloy that can switch between a metal and a half-metal. Thiseffect can provide tunable spintronics properties. Using the density functional theory (DFT) withreliable implementations of the electron correlation effec
ts, we find Mn2ScSi total energy curvesconsisting of distinct branches with a very small energy difference. The phase at low lattice crystalvolume is a low magnetic half-metallic state while the phase at high lattice crystal volume is a highmagnetic metallic state. We suggest that the transition between half-metallic and metallic statescan be triggered by a triaxial contraction/expansion of the crystal lattice or by an external magneticfield if we assume that the lattice is cubic and remains cubic under expansion/contraction. However,the phase at high volume can also undergo an austenite-martensite phase transition because of thepresence of Jahn-Teller active3delectrons on the Mn atoms.
Integrating multiple properties in a single system is crucial for the continuous developments in electronic devices. However, some physical properties are mutually exclusive in nature. Here, we report the coexistence of two seemingly mutually exclusi
ve properties-polarity and two-dimensional conductivity-in ferroelectric Ba$_{0.2}$Sr$_{0.8}$TiO$_3$ thin films at the LaAlO$_3$/Ba$_{0.2}$Sr$_{0.8}$TiO$_3$ interface at room temperature. The polarity of a ~3.2 nm Ba$_{0.2}$Sr$_{0.8}$TiO$_3$ thin film is preserved with a two-dimensional mobile carrier density of ~0.05 electron per unit cell. We show that the electronic reconstruction resulting from the competition between the built-in electric field of LaAlO$_3$ and the polarization of Ba$_{0.2}$Sr$_{0.8}$TiO$_3$ is responsible for this unusual two-dimensional conducting polar phase. The general concept of exploiting mutually exclusive properties at oxide interfaces via electronic reconstruction may be applicable to other strongly-correlated oxide interfaces, thus opening windows to new functional nanoscale materials for applications in novel nanoelectronics.
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