No Arabic abstract
We present a microscopic study of a doped quantum spin liquid candidate, the hyperkagome Na$_3$Ir$_3$O$_8$ compound by using $^{23}$Na NMR. We determine the intrinsic behavior of the uniform textbf{q} $ = 0$ susceptibility via shift measurements and the dynamical response by probing the spin-lattice relaxation rate. Throughout the studied temperature range, the susceptibility is consistent with a semimetal behavior, though with electronic bands substantially modified by correlations. Remarkably, the antiferromagnetic fluctuations present in the insulating parent compound Na$_4$Ir$_3$O$_8$ survive in the studied compound. The spin dynamics are consistent with 120$^o$ excitations modes displaying short-range correlations.
The complex iridium oxide Na3Ir3O8 with a B-site ordered spinel structure was synthesized in single crystalline form, where the chiral hyper-kagome lattice of Ir atoms, as observed in the spin-liquid candidate Na4Ir3O8, was identified. The average valence of Ir is 4.33+ and, therefore, Na3Ir3O8 can be viewed as a doped analogue of the hyper-kagome spin liquid with Ir4+. The transport measurements showed that Na3Ir3O8 is in fact a semi-metal. The electronic structure calculation demonstrated that the strong spin-orbit coupling of Ir yields the semi-metallic state out of an otherwise band insulating state, which may harbor exotic topological effects embedded in the hyper-kagome lattice.
The kagome Hubbard model (KHM) is a paradigmatic example of a frustrated two-dimensional model. While its strongly correlated regime, described by a Heisenberg model, is of topical interest due to its enigmatic prospective spin-liquid ground state, the weakly and moderately correlated regimes remain largely unexplored. Motivated by the rapidly growing number of metallic kagome materials (e.g., Mn$_3$Sn, Fe$_3$Sn$_2$, FeSn, Co$_3$Sn$_2$S$_2$, Gd$_3$Ru$_4$Al$_{12}$), we study the respective regimes of the KHM by means of three complementary numerical methods: the dynamical mean-field theory (DMFT), the dynamical vertex approximation (D$Gamma$A), and determinant quantum Monte Carlo (DQMC). In contrast to the archetypal square-lattice, we find no tendencies towards magnetic ordering, as magnetic correlations remain short-range. Nevertheless, the magnetic correlations undergo a remarkable crossover as the system approaches the metal-to-insulator transition. The Mott transition itself does however not affect the magnetic correlations. Our equal-time and dynamical structure factors can be used as a reference for inelastic neutron scattering experiments on the growing family of metallic kagome materials.
By using a combination of heteroepitaxial growth, structure refinement based on synchrotron x-ray diffraction and first-principles calculations, we show that the symmetry-protected Dirac line nodes in the topological semimetallic perovskite SrIrO3 can be lifted simply by applying epitaxial constraints. In particular, the Dirac gap opens without breaking the Pbnm mirror symmetry. In virtue of a symmetry-breaking analysis, we demonstrate that the original symmetry protection is related to the n-glide operation, which can be selectively broken by different heteroepitaxial structures. This symmetry protection renders the nodal line a nonsymmorphic Dirac semimetallic state. The results highlight the vital role of crystal symmetry in spin-orbit-coupled correlated oxides and provide a foundation for experimental realization of topological insulators in iridate-based heterostructures.
The realization of Kitaev spin liquid, where spins on a honeycomb lattice are coupled ferromagnetically by bond-dependent anisotropic interactions, has been a sought-after dream. 5d iridium oxides $alpha$-Li2IrO3 and $alpha$-Na2IrO3 with a honeycomb lattice of Jeff = 1/2 moments recently emerged as a possible materialization. Strong signature of Kitaev physics, however, was not captured. Here we report the discovery of a complex iridium oxide $beta$-Li2IrO3 with Jeff = 1/2 moments on hyper-honeycomb lattice, a three-dimensional analogue of honeycomb lattice. A positive Curie-Weiss temperature $theta_{CW}$ ~ 40 K indicated dominant ferromagnetic interactions among Jeff = 1/2 moments in $beta$-Li2IrO3. A magnetic ordering with a small entropy change was observed at Tc = 38 K, which, with the application of magnetic field of only 3 T, changed to a fully polarized state of Jeff = 1/2 moments. Those results imply that hyper-honeycomb beta-Li2IrO3 is located in the vicinity to a Kitaev spin liquid.
Temperature-dependent dynamical spin correlations, which can be readily accessed via a variety of experimental techniques, hold the potential of offering a unique fingerprint of quantum spin liquids and other intriguing dynamical states. In this work we present an in-depth study of the temperature-dependent dynamical spin structure factor $S({bf q}, omega)$ of the antiferromagnetic (AFM) Heisenberg spin-1/2 model on the kagome lattice with additional Dzyaloshinskii--Moriya (DM) interactions. Using the finite-temperature Lanczos method on lattices with up to $N = 30$ sites we find that even without DM interactions, chiral low-energy spin fluctuations of the $120^circ$ AFM order parameter dominate the dynamical response. This leads to a nontrivial frequency dependence of $S({bf q}, omega)$ and the appearance of a pronounced low-frequency mode at the M point of the extended Brillouin zone. Adding an out-of-plane DM interactions $D^z$ gives rise to an anisotropic dynamical response, a softening of in-plane spin fluctuations, and, ultimately, the onset of a coplanar AFM ground-state order at $D^z > 0.1 J$. Our results are in very good agreement with existing inelastic neutron scattering and temperature-dependent NMR spin-lattice relaxation rate ($1/T_1$) data on the paradigmatic kagome AFM herbertsmithite, where the effect of its small $D^z$ on the dynamical spin correlations is shown to be rather small, as well as with $1/T_1$ data on the novel kagome AFM YCu$_3$(OH)$_6$Cl$_3$, where its substantial $D^z approx 0.25 J$ interaction is found to strongly affect the spin dynamics.