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Register a new userOctupolar vs N{e}el Order in Cubic 5$d^2$ double perovskites
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We report time-of-flight neutron spectroscopic and diffraction studies of the 5$d^2$ cubic double pervoskite magnets, Ba$_2$MOsO$_6$ ($M$ = Zn, Mg, Ca). These cubic materials are all described by antiferromagnetically-coupled 5$d^2$ Os$^{6+}$ ions decorating a face-centred cubic (FCC) lattice. They all exhibit thermodynamic anomalies consistent with phase transitions at a temperature $T^*$, and exhibit a gapped magnetic excitation spectrum with spectral weight concentrated at wavevectors typical of type I antiferromagnetic orders. While muon spin resonance experiments show clear evidence for time reversal symmetry breaking, no corresponding magnetic Bragg scattering is observed at low temperatures. These results, consistent with low temperature octupolar or quadrupolar order, are discussed in the context of other 5$d^2$ DP magnets, and theories for $d^2$ ions on a FCC lattice which predict exotic orders driven by multipolar interactions.
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Conflicting interpretations of experimental data preclude the understanding of the quantum magnetic state of spin-orbit coupled d$^2$ double perovskites. Whether the ground state is a Janh-Teller-distorted order of quadrupoles or the hitherto elusive octupolar order remains debated. We resolve this uncertainty through direct calculations of all-rank inter-site exchange interactions and inelastic neutron scattering (INS) cross-section for the d$^2$ double perovskite series Ba$_2M$OsO$_6$ ($M$= Ca, Mg, Zn). Using advanced many-body first principles methods we show that the ground state is formed by ferro-ordered octupoles coupled within the ground-stated $E_g$ doublet. Computed ordering temperature of the single second-order phase-transition and gapped excitation spectra are fully consistent with observations. Minuscule distortions of the parent cubic structure are shown to qualitatively modify the structure of magnetic excitations.
Spin correlations in the pyrochlore antiferromagnet Y_2Ru_2O_7 with Curie-Weiss temperature $Theta_{CW}=-1100$ K and critical temperature T_N=77 K were examined through neutron scattering. For $T_N<T<Theta_{CW}/3$ the data show spin relaxation with a rate $hbarGamma= 1.17(9)k_BT$. For T<T_N spectral weight moves to higher energies with substantial changes up to $4times k_BT_N$. For T<<T_N there is a $Delta=11(1)$ meV energy gap and a pronounced spectral maximum at 19.7 meV. Throughout the temperature range examined the wave vector dependence of inelastic scattering exhibits a broad peak for $Qdapprox 3.8$ (d is Ru-Ru spacing) consistent with dipolar spin correlations.
Motivated by experimental and theoretical interest in realizing multipolar orders in $d$-orbital materials, we discuss the quantum magnetism of $J!=!2$ ions which can be realized in spin-orbit coupled oxides with $5d^2$ transition metal ions. Based on the crystal field environment, we argue for a splitting of the $J!=!2$ multiplet, leading to a low lying non-Kramers doublet which hosts quadrupolar and octupolar moments. We discuss a microscopic mechanism whereby the combined perturbative effects of orbital repulsion and antiferromagnetic Heisenberg spin interactions leads to ferro-octupolar coupling between neighboring sites, and stabilizes ferro-octupolar order for a face-centered cubic lattice. This same mechanism is also shown to disfavor quadrupolar ordering. We show that studying crystal field levels via Raman scattering in a magnetic field provides a probe of octupolar order. We study spin dynamics in the ferro-octupolar state using a slave-boson approach, uncovering a gapped and dispersive magnetic exciton. For sufficiently strong magnetic exchange, the dispersive exciton can condense, leading to conventional type-I antiferromagnetic (AFM) order which can preempt octupolar order. Our proposal for ferrooctupolar order, with specific results in the context of a model Hamiltonian, provides a comprehensive understanding of thermodynamics, $mu$SR, X-ray diffraction, and inelastic neutron scattering measurements on a range of cubic $5d^2$ double perovskite materials including Ba$_2$ZnOsO$_6$, Ba$_2$CaOsO$_6$, and Ba$_2$MgOsO$_6$. Our proposal for exciton condensation leading to type-I AFM order may be relevant to materials such as Sr$_2$MgOsO$_6$.
We present results for the phase diagram of an SU($N$) generalization of the Heisenberg antiferromagnet on a bipartite three-dimensional anisotropic cubic (tetragonal) lattice as a function of $N$ and the lattice anisotropy $gamma$. In the isotropic $gamma=1$ cubic limit, we find a transition from N{e}el to valence bond solid (VBS) between N=9 and N=10. We follow the N{e}el-VBS transition to the limiting cases of $gamma ll 1 $ (weakly coupled layers) and $gamma gg 1$ (weakly coupled chains). Throughout the phase diagram we find a direct first-order transition from N{e}el at small-$N$ to VBS at large-$N$. In the three-dimensional models studied here, we find no evidence for either an intervening spin-liquid photon phase or a continuous transition, even close to the limit $gamma ll 1$ where the isolated layers undergo continuous N{e}el-VBS transitions.
Quantum magnets with spin $J=2$, which arise in spin-orbit coupled Mott insulators, can potentially display multipolar orders. We carry out an exact diagonalization study of a simple octahedral crystal field Hamiltonian for two electrons, incorporating spin-orbit coupling (SOC) and interactions, finding that either explicitly including the $e_g$ orbitals, or going beyond the rotationally invariant Coulomb interaction within the $t_{2g}$ sector, causes a degeneracy breaking of the $J!=!2$ level degeneracy. This can lead to a low-lying non-Kramers doublet carrying quadrupolar and octupolar moments and an excited triplet which supports magnetic dipole moments, bolstering our previous phenomenological proposal for the stabilization of ferro-octupolar order in heavy transition metal oxides. We show that the spontaneous time-reversal symmetry breaking due to ferro-octupolar ordering within the non-Kramers doublet leads to electronic orbital loop currents. The resulting internal magnetic fields can potentially explain the small fields inferred from muon-spin relaxation ($mu$SR) experiments on cubic $5d^2$ osmate double perovskites Ba$_2$ZnOsO$_6$, Ba$_2$CaOsO$_6$, and Ba$_2$MgOsO$_6$, which were previously attributed to weak dipolar magnetism. We make further predictions for oxygen NMR experiments on these materials. We also study the reversed level scheme, where the $J!=!2$ multiplet splits into a low-lying magnetic triplet and excited non-Kramers doublet, presenting single-ion results for the magnetic susceptibility in this case, and pointing out its possible relevance for the rhenate Ba$_2$YReO$_6$. Our work highlights the intimate connection between the physics of heavy transition metal oxides and that of $f$-electron based heavy fermion compounds.
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