No Arabic abstract
The hyperkagome antiferromagnet Na$_{4}$Ir$_3$O$_8$ represents the first genuine candidate for the realisation of a three-dimensional quantum spin-liquid. It can also be doped towards a metallic state, thus offering a rare opportunity to explore the nature of the metal-insulator transition in correlated, frustrated magnets. Here we report thermodynamic and transport measurements in both metallic and weakly insulating single crystals down to 150 mK. While in the metallic sample the phonon thermal conductivity ($kappa^{ph}$) is almost in the boundary scattering regime, in the insulating sample we find a large reduction $kappa^{ph}$ over a very wide temperature range. This result can be ascribed to the scattering of phonons off nanoscale disorder or off the gapless magnetic excitations that are seen in the low-temperature specific heat. This works highlights the peculiarity of the metal-insulator transition in Na$_{3+x}$Ir$_3$O$_8$ and demonstrates the importance of the coupling between lattice and spin degrees of freedom in the presence of strong spin-orbit coupling.
We develop high temperature series expansions for $ln{Z}$ and the uniform structure factor of the spin-half Heisenberg model on the hyperkagome lattice to order $beta^{16}$. These expansions are used to calculate the uniform susceptibility ($chi$), the entropy ($S$), and the heat capacity ($C$) of the model as a function of temperature. Series extrapolations of the expansions converge well down to a temperature of approximately $J/4$. A comparison with the experimental data for Na$_4$Ir$_3$O$_8$ shows that its magnetic susceptibility is reasonably well described by the model with an exchange constant $Japprox 300 K$, but there are also additional smaller terms present in the system. The specific heat of the model has two peaks. The lower temperature peak, which is just below our range of convergence contains about 40 percent of the total entropy. Despite being a 3-dimensional lattice, this model shares many features with the kagome lattice Heisenberg model and the material must be considered a strong candidate for a quantum spin-liquid.
The optical properties of a V4O7 single crystal have been investigated from the high temperature metallic phase down to the low temperature antiferromagnetic insulating one. The temperature dependent behavior of the optical conductivity across the metal-insulator transition (MIT) can be explained in a polaronic scenario. Charge carriers form strongly localized polarons in the insulating phase as suggested by a far-infrared charge gap abruptly opening at T_MIT = 237 K. In the metallic phase instead the presence of a Drude term is indicative of fairly delocalized charges with a moderately renormalized mass m* = 5m_e. The electronic spectral weight is almost recovered on an energy scale of 1 eV, which is much narrower compared to VO2 and V2O3 cases. Those findings suggest that electron-lattice interaction rather than electronic correlation is the driving force for V4O7 metal-insulator transition.
The celebrated Wiedemann-Franz (WF) law is believed to be robust in metals as long as interactions between electrons preserve their fermion-quasiparticle character. We study thermal transport and the fate of the WF law close to a continuous metal-insulator transition (MIT) in the Falicov-Kimball model (FKM) using cluster-dynamical mean-field theory (CDMFT). Surprisingly, as for electrical transport, we find robust and novel quantum critical scaling in thermal transport across the MIT. We unearth the deeper reasons for these novel findings in terms of (i) the specific structure of energy-current correlations for the FKM and (ii) the microscopic electronic processes which facil- itate energy transport while simultaneously blocking charge transport close to the MIT. However, within (C)DMFT, we also find that the WF law survives at T=0 in the incoherent metal right up to the MIT, even in absence of Landau quasiparticles.
We report on the effects of introducing magnetic and non-magnetic disorder in the hyperkagome iridate quantum spin liquid (QSL) candidate Na$_4$Ir$_3$O$_8$ by partially replacing Ir$^{4+}$ ($S = 1/2$) with Ru$^{4+}$ ($S = 1$) or Ti$^{4+}$ ($S = 0$). Specifically, we synthesized Na$_4$(Ir$_{1-x}$Ru$_x$)$_3$O$_8 (x = 0.05, 0.10, 0.2, 0.3)$ and Na$_4$Ir$_{2.7}$Ti$_{0.3}$O$_8$ samples and measured electrical transport, AC and DC magnetization, and heat capacity down to $T = 1.8$ K. Na$_4$Ir$_3$O$_8$ is associated with a large Weiss temperature $theta = -650$ K, a broad anomaly in magnetic heat capacity C$_{mag}$ at T $approx25$ K, low temperature power-law heat capacity, and spin glass freezing below $T_f approx 6$ K. We track the change in these characteristic features as Ir is partially substituted by Ru or Ti. We find that for Ru substitution, $theta$ increases and stays negative, the anomaly in C$_{mag}$ is suppressed in magnitude and pushed to lower temperatures, low temperature $C sim T^alpha$ with $alpha$ between $2$ and $3$ and decreasing towards $2$ with increasing $x$, and $T_f$ increases with increase in Ru concentration $x$. For Ti substitution we find that $theta$ and T$_f$ become smaller and the anomaly in $C_{mag}$ is completely suppressed. In addition, introducing non-magnetic Ti leads to the creation of orphan spins which show up in the low temperature magnetic susceptibility.
Recent experiments indicate that Na$_4$Ir$_3$O$_8$, a material in which s=1/2 iridium local moments form a three dimensional network of corner-sharing triangles, may have a quantum spin liquid ground state with gapless spin excitations. Using a combination of exact diagonalization, symmetry analysis of fermionic mean field ground states and Gutzwiller projected variational wavefunction studies, we propose a quantum spin liquid with spinon Fermi surfaces as a favorable candidate for the ground state of the Heisenberg model on the hyper-kagome lattice of Na$_4$Ir$_3$O$_8$. We present a renormalized mean field theory of the specific heat of this spin liquid and also discuss possible low temperature instabilities of the spinon Fermi surfaces.