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Register a new userSpin order and dynamics in the diamond-lattice Heisenberg antiferromagnets CuRh2O4 and CoRh2O4
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Antiferromagnetic insulators on the diamond lattice are candidate materials to host exotic magnetic phenomena ranging from spin-orbital entanglement to degenerate spiral ground-states and topological paramagnetism. Compared to other three-dimensional networks of magnetic ions, such as the geometrically frustrated pyrochlore lattice, the investigation of diamond-lattice magnetism in real materials is less mature. In this work, we characterize the magnetic properties of model A-site spinels CoRh2O4 (cobalt rhodite) and CuRh2O4 (copper rhodite) by means of thermo-magnetic and neutron scattering measurements and perform group theory analysis, Rietveld refinement, mean-field theory, and spin wave theory calculations to analyze the experimental results. Our investigation reveals that cubic CoRh2O4 is a canonical S=3/2 diamond-lattice Heisenberg antiferromagnet with a nearest neighbor exchange J = 0.63 meV and a Neel ordered ground-state below a temperature of 25 K. In tetragonally distorted CuRh2O4, competiting exchange interactions between up to third nearest-neighbor spins lead to the development of an incommensurate spin helix at 24 K with a magnetic propagation vector k = (0,0,0.79). Strong reduction of the ordered moment is observed for the S=1/2 spins in CuRh2O4 and captured by our 1/S corrections to the staggered magnetization. Our work identifies CoRh2O4 and CuRh2O4 as reference materials to guide future work searching for exotic quantum behavior in diamond-lattice antiferromagnets.
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Single crystal neutron diffraction, inelastic neutron scattering, bulk magnetization measurements, and first-principles calculations are used to investigate the magnetic properties of the honeycomb lattice $rm Tb_2Ir_3Ga_9$. While the $Rln2$ magnetic contribution to the low-temperature entropy indicates a $rm J_{eff}=1/2$ moment for the lowest-energy crystal-field doublet, the Tb$^{3+}$ ions form a canted antiferromagnetic structure below 12.5 K. Due to the Dzyalloshinskii-Moriya interactions, the Tb moments in the $ab$ plane are slightly canted towards $b$ by $6^circ$ with a canted moment of 1.22 $mu_{rm B} $ per formula unit. A minimal $xxz$ spin Hamiltonian is used to simultaneously fit the spin-wave frequencies along the high symmetry directions and the field dependence of the magnetization along the three crystallographic axes. Long-range magnetic interactions for both in-plane and out-of-plane couplings up to the second nearest neighbors are needed to account for the observed static and dynamic properties. The $z$ component of the exchange interactions between Tb moments are larger than the $x$ and $y$ components. This compound also exhibits bond-dependent exchange with negligible nearest exchange coupling between moments parallel and perpendicular to the 4$f$ orbitals. Despite the $J_{{rm eff}}=1/2$ moments, the spin Hamiltonian is denominated by a large in-plane anisotropy $K_z sim -1$ meV. DFT calculations confirm the antiferromagnetic ground state and the substantial inter-plane coupling at larger Tb-Tb distances.
The correlated spin dynamics and the temperature dependence of the correlation length $xi(T)$ in two-dimensional quantum ($S=1/2$) Heisenberg antiferromagnets (2DQHAF) on square lattice are discussed in the light of experimental results of proton spin lattice relaxation in copper formiate tetradeuterate (CFTD). In this compound the exchange constant is much smaller than the one in recently studied 2DQHAF, such as La$_2$CuO$_4$ and Sr$_2$CuO$_2$Cl$_2$. Thus the spin dynamics can be probed in detail over a wider temperature range. The NMR relaxation rates turn out in excellent agreement with a theoretical mode-coupling calculation. The deduced temperature behavior of $xi(T)$ is in agreement with high-temperature expansions, quantum Monte Carlo simulations and the pure quantum self-consistent harmonic approximation. Contrary to the predictions of the theories based on the Non-Linear $sigma$ Model, no evidence of crossover between different quantum regimes is observed.
Counterintuitive order-disorder phenomena emerging in antiferromagnetically coupled spin systems have been reported in various studies. Here we perform a systematic effective field theory analysis of two-dimensional bipartite quantum Heisenberg antiferromagnets subjected to either mutually aligned -- or mutually orthogonal -- magnetic and staggered fields. Remarkably, in the aligned configuration, the finite-temperature uniform magnetization $M_T$ grows as temperature rises. Even more intriguing, in the orthogonal configuration, $M_T$ first drops, goes through a minimum, and then increases as temperature rises. Unmasking the effect of the magnetic field, we furthermore demonstrate that the finite-temperature staggered magnetization $M^H_s$ and entropy density -- both exhibiting non-monotonic temperature dependence -- are correlated. Interestingly, in the orthogonal case, $M^H_s$ presents a maximum, whereas in mutually aligned magnetic and staggered fields, $M^H_s$ goes through a minimum. The different behavior can be traced back to the existence of an easy XY-plane that is induced by the magnetic field in the orthogonal configuration.
The spin-wave excitation spectrum, the magnetization, and the N{e}el temperature for the quasi-two-dimensional spin-1/2 antiferromagnetic Heisenberg model with compass-model interaction in the plane proposed for iridates are calculated in the random phase approximation. The spin-wave spectrum agrees well with data of Lanczos diagonalization. We find that the Neel temperature is enhanced by the compass-model interaction and is close to the experimental value for Ba2IrO4.
Thermodynamic properties of a spin ice model on a Kagome lattice are obtained from dynamic simulations and compared with properties in square lattice spin ice. The model assumes three-component Heisenberg-like dipoles of an array of planar magnetic islands situated on a Kagome lattice. Ising variables are avoided. The island dipoles interact via long-range dipolar interactions and are restricted in their motion due to local shape anisotropies. We define various order parameters and obtain them and thermodynamic properties from the dynamics of the system via a Langevin equation, solved by the Heun algorithm. Generally, a slow cooling from high to low temperature does not lead to a particular state of order, even for a set of coupling parameters that gives well thermalized states and dynamics. Some suggestions are proposed for the alleviation of the geometric frustration effects and for the generation of local order in the low temperature regime.
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