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تسجيل مستخدم جديدPrediction of Stoner-Type Magnetism in Low-Dimensional Electrides
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Electrides are special ionic solids with excess cavity-trapped electrons serving as anions. Despite the extensive studies on electrides, the interplay between electrides and magnetism is not well understood due to the lack of stable magnetic electrides, particularly the lack of inorganic magnetic electrides. Here, based on the mechanism of Stoner-type magnetic instability, we propose that in certain electrides the low-dimensionality can facilitate the formation of magnetic ground state because of the enhanced density of states near the Fermi level. To be specific, A5B3 (A = Ca, Sr, Ba; B = As, Sb, Bi) (1D), Sr11Mg2Si10 (0D), Ba7Al10 (0D) and Ba4Al5 (0D) have been identified as stable magnetic electrides with spin-polarization energies of tens to hundreds of meV per formula unit. Especially for Ba5As3, the spin-polarization energy can reach up to 220 meV. Furthermore, we demonstrate that the magnetic moment and spin density mainly derive from the interstitial anionic electrons near the Fermi level. Our work paves a way to the searching of stable magnetic electrides and further exploration of the magnetic properties and related applications in electrides.
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Electrides are an emerging class of materials with excess electrons localized in interstices and acting as anionic interstitial quasi-atoms (ISQs). The spatial ion-electron separation means that electrides can be treated physically as ionic crystals,
and this unusual behavior leads to extraordinary physical and chemical phenomena. Here, a completely different effect in electrides is predicted. By recognizing the long-range Coulomb interactions between matrix atoms and ISQs that are unique in electrides, a nonanalytic correction to the forces exerted on matrix atoms is proposed. This correction gives rise to an LA-TA splitting in the acoustic branch of lattice phonons near the zone center, similar to the well-known LO-TO splitting in the phonon spectra of ionic compounds. The factors that govern this splitting are investigated, with isotropic fcc-Li and anisotropic hP4-Na as the typical examples. It is found that not all electrides can induce a detectable splitting, and criteria are given for this type of splitting. The present prediction unveils the rich phenomena in electrides and could lead to unprecedented applications.
We propose a design scheme for potential electrides derived from conventional materials. Starting with rare-earth-based ternary halides, we exclude halogens and perform global structure optimization to obtain thermodynamically stable or metastable ph
ases but having an excess of electrons confined inside interstitial cavities. Then, spin-polarized interstitial states are induced by chemical substitution with magnetic lanthanides. To demonstrate the capability of our approach, we test with 11 ternary halides and successfully predict 30 stable and metastable phases of nonmagnetic electrides subject to 3 different stoichiometric categories, and successively 28 magnetic electrides via chemical substitution with Gd. 56 out of these 58 designed electrides are discovered for the first time. Two electride systems, the monoclinic $A$C ($A=$ La, Gd) and the orthorhombic $A_2$Ge ($A=$ Y, Gd), are thoroughly studied to exemplify the set of predicted crystals. Interestingly, both systems turn out to be topological nodal line electrides (TNLE) in the absence of spin-orbit coupling and manifest spin-polarized interstitial states in the case of $A=$ Gd. Our work establishes a novel computational approach of functional electrides design and highlights the magnetism and topological phases embedded in electrides.
It is commonly believed that in typical collinear antiferromagnets, with no net magnetization, the energy bands are spin-(Kramers-degenerate. The opposite case is usually associated with a global time-reversal symmetry breaking (e.g., via ferro(i)mag
netism), or with the spin-orbit interaction is combined with the broken spatial inversion symmetry. Recently, another type of spin splitting was demonstrated to emerge in some fully compensated by symmetry, nonrelativistic, collinear magnets, and not even necessarily non-centrosymmetric. These materials feature non-zero spin density staggered not only in real, but also in momentum space. This duality results in a combination of characteristics typical of ferro- and antiferromagnets. Here we discuss this novel concept in application to a well-known semiconductor, FeSb2, and predict that upon certain alloying it becomes magnetic, and features such magnetic duality. The calculated energy bands split antisymmetrically with respect to spin degenerate nodal surfaces (and not nodal points, as in the case of spin-orbit splitting. This combination of a large (0.2 eV) spin splitting, compensated net magnetization and metallic ground-state, and a particular magnetic easy axis generate a large anomalous Hall conductivity (~150 S/cm) and a sizable magneto-optical Kerr effect, all deemed to be hallmarks of nonzero net magnetization. We identify a large contribution to the anomalous response originating from the spin-orbit interaction gapped anti-Kramers nodal surfaces, a mechanism distinct from the nodal lines and Weyl {it points} in ferromagnets.
The recently developed theory of topological quantum chemistry (TQC) has built a close connection between band representations in momentum space and orbital characters in real space. It provides an effective way to diagnose topological materials, lea
ding to the discovery of lots of topological materials after the screening of all known nonmagnetic compounds. On the other hand, it can also efficiently reveal spacial orbital characters, including average charge centers and site-symmetry characters. By using TQC theory with the computed irreducible representations in the first-principles calculations, we demonstrate that the electrides with excess electrons serving as anions at vacancies can be well identified by analyzing band representations (BRs), which cannot be expressed as a sum of atomic-orbital-induced band representations (aBRs). In fact, the floating bands (formed by the excess electrons) belong to the BRs induced from the pseudo-orbitals centered at vacancies. In other words, the electrides are proved to be unconventional ionic crystals, where a set of occupied bands is not a sum of aBRs but necessarily contains a BR from vacancies. The TQC theory provides a promising avenue to pursue more electride candidates in ionic crystals.
Plasmon opens up the possibility to efficiently couple light and matter at sub-wavelength scales. In general, the plasmon frequency is dependent of carrier density. This dependency, however, renders fundamentally a weak plasmon intensity at low frequ
ency, especially for Dirac plasmon (DP) widely studied in graphene. Here we demonstrate a new type of DP, excited by a Dirac nodal-surface state, which exhibits an anomalously density-independent frequency. Remarkably, we predict realization of anomalous DP (ADP) in 1D topological electrides, such as Ba3CrN3 and Sr3CrN3, by first-principles calculations. The ADPs in both systems have a density-independent frequency and high intensity, and their frequency can be tuned from terahertz to mid-infrared by changing the excitation direction. Furthermore, the intrinsic weak electron-phonon coupling of anionic electrons in electrides affords an added advantage of ultra-low phonon-assisted damping and hence a long lifetime of the ADPs. Our work paves the way to developing novel plasmonic and optoelectronic devices by combining topological physics with electride materials.
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