Antiferromagnetically coupled S=1/2 spins on an isotropic triangular lattice is the paradigm of frustrated quantum magnetism, but structurally ideal realizations are rare. Here we investigate NaYbO2, which hosts an ideal triangular lattice of Jeff=1/2 moments with no inherent site disorder. No signatures of conventional magnetic order appear down to 50 mK, strongly suggesting a quantum spin liquid ground state. We observe a two-peak specific heat and a nearly quadratic temperature dependence in accord with expectations for a two-dimensional Dirac spin liquid. Application of a magnetic field strongly perturbs the quantum disordered ground state and induces a clear transition into a collinear ordered state consistent with a long-predicted "up-up-down" structure for a triangular lattice XXZ Hamiltonian driven by quantum fluctuations. The observation of spin liquid signatures in zero field and quantum-induced ordering in intermediate fields in the same compound demonstrate an intrinsically quantum disordered ground state. We conclude that NaYbO2 is a model, versatile platform for exploring spin liquid physics with full tunability of field and temperature.Exotic ground states of quantum antiferromagnets are encouraged by the combination of low dimensionality, geometric frustration, and inherent anisotropies. Planar triangular lattices have long been sought as platforms for stabilizing them 1-7 ; however, ideal manifestations that do not break crystallographic or exchange symmetries upon approaching the quantum regime are rare. The organic compounds κ-(BEDT-TTF)2Cu2(CN)3 8 and EtMe3Sb[Pd(dmit)2]2 9 are two promising examples of triangular lattices with S=1/2 moments and a dynamically disordered spin ground state. However, S=1/2 inorganic analogs such as Ba3CoSb2O9 10 , Ba8CoNb6O24 11 , and NaTiO2 12-14 either order magnetically or undergo a lattice deformation and dimerization upon cooling. A key roadblock in inorganic systems is the identification of a material with a high crystallographic symmetry, rigid structure, and minimal defect mechanisms that also contains magnetic ions possessing strong quantum fluctuations. Ideally, the magnetic ions should be located at high symmetry positions that preclude antisymmetric Dzyaloshinskii-Moriya exchange from lifting geometric frustration at low temperatures.As an alternative to S=1/2 based compounds, rare earth ions with ground state doublets may also engender enhanced quantum fluctuations when decorating a triangular lattice. Specifically, recent studies have shown that the spin-orbit entangled Jeff=1/2 moments of Yb 3+ ions on this lattice may exhibit a variety of nearly degenerate magnetic states 15-22 . Given the appropriate anisotropies and when driven close

The evolution of the electronic properties of electron-doped (Sr1−xLax)2IrO4 is experimentally explored as the doping limit of La is approached. As electrons are introduced, the electronic ground state transitions from a spin-orbit Mott phase into an electronically phase separated state, where long-range magnetic order vanishes beyond x = 0.02 and charge transport remains percolative up to the limit of La substitution (x ≈ 0.06). In particular, the electronic ground state remains inhomogeneous even beyond the collapse of the parent state's long-range antiferromagnetic order, while persistent short-range magnetism survives up to the highest La-substitution levels. Furthermore, as electrons are doped into Sr2IrO4, we observe the appearance of a low temperature magnetic glass-like state intermediate to the complete suppression of antiferromagnetic order. Universalities and differences in the electron-doped phase diagrams of single layer and bilayer Ruddlesden-Popper strontium iridates are discussed.

Hybrid main group halide perovskites hold great technological promise in optoelectronic applications and present rich and complex evolution of structure and dynamics. Here we present low-temperature dielectric measurements and calorimetry of APbI3 [A = CH3NH3 +, HC­(NH2)2 +] that suggest glassy behavior on cooling. In both compounds, the dielectric loss displays frequency-dependent peaks below 100 K characteristic of a glassy slowing of relaxation dynamics, with HC­(NH2)2PbI3 exhibiting greater glass fragility. Consistent with quenched disorder, the low-temperature heat capacity of both perovskites deviates substantially from the ∼T 3 acoustic phonon contribution predicted by the Debye model. We suggest that static disorder of the A-site molecular cation, potentially coupled to local distortions of the Pb–I sublattice, is responsible for these phenomena. The distinct low-temperature dynamics observed in these two perovskites suggest qualitative differences in the interaction between the molecular cation and the surrounding inorganic framework, with potential implications for defect screening and device performance at ambient temperatures.

Neutron diffraction measurements are presented exploring the magnetic and structural phase behaviors of the candidate J ef f = 1/2 Mott insulating iridate Sr2IrO4. Comparisons are drawn between the correlated magnetism in this single layer system and its bilayer analog Sr3Ir2O7 where both materials exhibit magnetic domains originating from crystallographic twinning and comparable moment sizes. Weakly temperature dependent superlattice peaks violating the reported tetragonal space group of Sr2IrO4 are observed supporting the notion of a lower structural symmetry arising from a high temperature lattice distortion, and we use this to argue that moments orient along a unique in-plane axis demonstrating an orthorhombic symmetry in the resulting spin structure. Our results demonstrate that the correlated spin order and structural phase behaviors in both single and bilayer Srn+1IrnO3n+1 systems are remarkably similar and suggest comparable correlation strengths in each system.

Vous avez des questions? Nous pouvons vous aider. Pour communiquer directement avec un auteur, consultez la première page de la revue dans laquelle son article a été publié afin de trouver ses coordonnées. Si vous n'arrivez pas à les repérer, communiquez avec nous à PublicationsArchive-ArchivesPublications@nrc-cnrc.gc.ca. Questions? Contact the NRC Publications Archive team atPublicationsArchive-ArchivesPublications@nrc-cnrc.gc.ca. If you wish to email the authors directly, please see the first page of the publication for their contact information. NRC Publications Archive Archives des publications du CNRCThis publication could be one of several versions: author's original, accepted manuscript or the publisher's version. / La version de cette publication peut être l'une des suivantes : la version prépublication de l'auteur, la version acceptée du manuscrit ou la version de l'éditeur. NRC Publications Record / Notice d'Archives des publications de CNRC:http://nparc.cisti-icist.nrc-cnrc.gc.ca/eng/view/object/?id=52705cc0-e17a-4735-a2b2-c0250cf7e564 http://nparc.cisti-icist.nrc-cnrc.gc.ca/fra/voir/objet/?id=52705cc0-e17a-4735-a2b2-c0250cf7e564 The electronic phase diagram of the weak spin-orbit Mott insulator (Sr 1−x La x Þ 3 Ir 2 O 7 is determined via an exhaustive experimental study. Upon doping electrons via La substitution, an immediate collapse in resistivity occurs along with a narrow regime of nanoscale phase separation comprised of antiferromagnetic, insulating regions and paramagnetic, metallic puddles persisting until x ≈ 0.04. Continued electron doping results in an abrupt, first-order phase boundary where the Néel state is suppressed and a homogenous, correlated, metallic state appears with an enhanced spin susceptibility and local moments. As the metallic state is stabilized, a weak structural distortion develops and suggests a competing instability with the parent spin-orbit Mott state. First-Order Melting of a Weak Spin-Orbit Mott Insulator into a Correlated Metal

Interest in many strongly spin-orbit-coupled 5d-transition metal oxide insulators stems from mapping their electronic structures to a J eff ¼ 1/2 Mott phase. One of the hopes is to establish their Mott parent states and explore these systems' potential of realizing novel electronic states upon carrier doping. However, once doped, little is understood regarding the role of their reduced Coulomb interaction U relative to their strongly correlated 3d-electron cousins. Here we show that, upon hole-doping a candidate J eff ¼ 1/2 Mott insulator, carriers remain localized within a nanoscale phase-separated ground state. A percolative metal-insulator transition occurs with interplay between localized and itinerant regions, stabilizing an antiferromagnetic metallic phase beyond the critical region. Our results demonstrate a surprising parallel between doped 5d-and 3d-electron Mott systems and suggest either through the near-degeneracy of nearby electronic phases or direct carrier localization that U is essential to the carrier response of this doped spin-orbit Mott insulator.

Through a neutron scattering, charge transport, and magnetization study, the correlated ground state in the bilayer iridium oxide Sr3Ir2O7 is explored. Our combined results resolve scattering consistent with a high temperature magnetic phase that persists above 600 K, reorients at the previously defined TAF = 280 K, and coexists with an electronic ground state whose phase behavior suggests the formation of a fluctuating charge or orbital phase that freezes below T * ≈ 70 K.Our study provides a window into the emergence of multiple electronic order parameters near the boundary of the metal to insulator phase transition of the 5d J ef f = 1/2 Mott phase.

We report a combined muon spin relaxation/rotation, bulk magnetization, neutron scattering, and transport study of the electronic properties of the pyrochlore iridate Nd 2 Ir 2 O 7 . We observe the onset of strongly hysteretic behavior in the temperature dependent magnetization below 120 K, and an abrupt increase in the temperature dependent resistivity below 8 K. Zero field muon spin relaxation measurements show that the hysteretic magnetization is driven by a transition to a magnetically disordered state, and that below 8 K a complex magnetically ordered ground state sets in, as evidenced by the onset of heavily damped spontaneous muon precession. Our measurements point toward the absence of a true metal-to-insulator phase transition in this material and suggest that Nd 2 Ir 2 O 7 lies either within or on the metallic side of the boundary of the Dirac semimetal regime within its topological phase diagram.