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Register a new userNematic Spin Liquid State in the $S=frac{5}{2}$ Heisenberg Kagome Antiferromagnet Li$_9$Fe$_3$(P$_2$O$_7$)$_3$(PO$_4$)$_2$
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We investigate the low temperature magnetic properties of a $S=frac{5}{2}$ Heisenberg kagome antiferromagnet, the layered monodiphosphate Li$_9$Fe$_3$(P$_2$O$_7$)$_3$(PO$_4$)$_2$, using magnetization measurements and $^{31}$P nuclear magnetic resonance. An antiferromagnetic-type order sets in at $T_{rm N}=1.3$ K and a characteristic magnetization plateau is observed at 1/3 of the saturation magnetization below $T^* sim 5$ K. A moderate $^{31}$P NMR line broadening reveals the development of anisotropic short-range correlations within the plateau phase concomitantly with a gapless spin-lattice relaxation time $T_1 sim k_B T / hbar S$, which both point to the presence of a semiclassical nematic spin liquid state predicted for the Heisenberg kagome antiferromagnetic model.
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We report on thermodynamic, magnetization, and muon spin relaxation measurements of the strong spin-orbit coupled iridate Ba$_3$IrTi$_2$O$_9$, which constitutes a new frustration motif made up a mixture of edge- and corner-sharing triangles. In spite of strong antiferromagnetic exchange interaction of the order of 100~K, we find no hint for long-range magnetic order down to 23 mK. The magnetic specific heat data unveil the $T$-linear and -squared dependences at low temperatures below 1~K. At the respective temperatures, the zero-field muon spin relaxation features a persistent spin dynamics, indicative of unconventional low-energy excitations. A comparison to the $4d$ isostructural compound Ba$_3$RuTi$_2$O$_9$ suggests that a concerted interplay of compass-like magnetic interactions and frustrated geometry promotes a dynamically fluctuating state in a triangle-based iridate.
Magnetic properties and magnetic structure of the Ba$_{2}$Mn(PO$_{4}$)$_{2}$ antiferromagnet featuring frustrated zigzag chains of $S=frac{5}{2}$ Mn$^{2+}$ ions are reported based on neutron diffraction, density-functional band-structure calculations, as well as temperature- and field-dependent measurements of the magnetization and specific heat. A magnetic transition at $T_Nsimeq 5$,K marks the onset of the antiferromagnetic order with the propagation vector ${mathbf k} = (frac12, 0, frac12)$ and ordered moment of $4.33pm0.08~mu_B$/Mn$^{2+}$ at 1.5,K, pointing along the $c$ direction. Direction of the magnetic moment is chosen by the single-ion anisotropy, which is relatively weak compared to the isostructural Ni$^{2+}$ compound. Geometrical frustration has strong impact on thermodynamic properties of Ba$_2$Mn(PO$_4)_2$, but manifestations of the frustration are different from those in Ba$_2$Ni(PO$_4)_2$, where frustration by isotropic exchange couplings is minor, yet strong and competing single-ion anisotropies are present. A spin-flop transition is observed around 2.5,T. The evaluation of the magnetic structure from the ground state via the spin-flop state to the field-polarized ferromagnetic state has been revealed by a comprehensive neutron diffraction study as a function of magnetic field below $T_N$. Finally, a magnetic phase diagram in the $H-T$ plane is obtained.
We have discovered a novel candidate for a spin liquid state in a ruthenium oxide composed of dimers of $S = $ 3/2 spins of Ru$^{5+}$,Ba$_3$ZnRu$_2$O$_9$. This compound lacks a long range order down to 37 mK, which is a temperature 5000-times lower than the magnetic interaction scale of around 200 K. Partial substitution for Zn can continuously vary the magnetic ground state from an antiferromagnetic order to a spin-gapped state through the liquid state. This indicates that the spin-liquid state emerges from a delicate balance of inter- and intra-dimer interactions, and the spin state of the dimer plays a vital role. This unique feature should realize a new type of quantum magnetism.
Structure with orbital degeneracy is unstable toward spontaneous distortion. Such orbital correlation usually has a much higher energy scale than spins, and therefore, magnetic transition takes place at a much lower temperature, almost independently from orbital ordering. However, when the energy scales of orbitals and spins meet, there is a possibility of spin-orbital entanglement that would stabilize novel ground state such as spin-orbital liquid and random singlet state. Here we review on such a novel spin-orbital magnetism found in the hexagonal perovskite oxide Ba$_3$CuSb$_2$O$_9$, which hosts a self-organized honeycomblike short-range order of a strong Jahn-Teller ion Cu$^{2+}$. Comprehensive structural and magnetic measurements have revealed that the system has neither magnetic nor Jahn-Teller transition down to the lowest temperatures, and Cu spins and orbitals retain the hexagonal symmetry and paramagnetic state. Various macroscopic and microscopic measurements all indicate that spins and orbitals remain fluctuating down to low temperatures without freezing, forming a spin-orbital entangled liquid state.
Here, we report both ac and dc magnetization, thermodynamic and electric properties of hexagonal Ba$_3$NiIr$_2$O$_9$. The Ni$^{2+}$ (spin-1) forms layered triangular-lattice and interacts antiferromagnetically while Ir$^{5+}$ is believed to act as magnetic link between the layers. This complex magnetic interaction results in magnetic frustration leading to a spin-glass transition at $T_f$ $sim$ 8.5 K. The observed magnetic relaxation and aging effect also confirms the nonequilibrium ground state. The system further shows large exchange bias which is tunable with cooling field. Below the Curie-Weiss temperature $theta_{CW}$ ($sim$ -29 K), the magnetic specific heat $C_m$ displays a broad hump and at low temperature follows $C_m = gamma T^alpha$ dependence where both $gamma$ and $alpha$ show dependence on temperature and magnetic field. A sign change in magnetoresistace is observed which is due to an interplay among magnetic moment, field and spin-orbit coupling.
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