The ruthenium halide $alpha$-RuCl$_{3}$ is a promising candidate for a Kitaev spin liquid. However, the microscopic model describing $alpha$-RuCl$_{3}$ is still debated partly because of a lack of analogue materials for $alpha$-RuCl$_{3}$, which prev
ents tracking of electronic properties as functions of controlled interaction parameters. Here, we report a successful synthesis of RuBr$_{3}$. The material RuBr$_{3}$~possesses BiI$_3$-type structure (space group: $Roverline{3}$) where Ru$^{3+}$ form an ideal honeycomb lattice. Although RuBr$_{3}$ has a negative Weiss temperature, it undergoes a zigzag antiferromagnetic transition at $T_mathrm{N}=34$ K, as does $alpha$-RuCl$_{3}$. Our analyses indicate that the Kitaev and non-Kitaev interactions can be modified in ruthenium trihalides by changing the ligand sites, which provides a new platform for exploring Kitaev spin liquids.
The search for topological insulators has been actively promoted in the field of condensed matter physics for further development in energy-efficient information transmission and processing. In this context, recent studies have revealed that not only
electrons but also bosonic particles such as magnons can construct edge states carrying nontrivial topological invariants. Here we demonstrate topological triplon bands in the spin-1/2 two-dimensional dimerized quantum antiferromagnet Ba$_2$CuSi$_2$O$_6$Cl$_2$, which is closely related to a pseudo-one-dimensional variant of the Su-Schrieffer-Heeger (SSH) model, through inelastic neutron scattering experiments. The excitation spectrum exhibits two triplon bands and a clear band gap between them due to a small alternation in interdimer exchange interactions along the $a$-direction, which is consistent with the crystal structure. The presence of topologically protected edge states is indicated by a bipartite nature of the lattice.
In an ideal classical pyrochlore antiferromagnet without perturbations, an infinite degeneracy at a ground state leads to absence of a magnetic order and spin-glass transition. Here we present Na$_3$Mn(CO$_3$)$_2$Cl as a new candidate compound where
classical spins are coupled antiferromagnetically on the pyrochlore lattice, and report its structural and magnetic properties.The temperature dependences of the magnetic susceptibility and heat capacity, and the magnetization curve are consistent with those of an $S$ = 5/2 pyrochlore lattice antiferromagnet with nearest-neighbor interactions of 2 K. Neither an apparent signature of a spin-glass transition nor a magnetic order is detected in magnetization and heat capacity measurements, or powder neutron diffraction experiments. On the other hand, an antiferromagnetic short-range order from the nearest neighbors is evidenced by the $Q$-dependence of the diffuse scattering which develops around 0.85 AA$^{-1}$. A high degeneracy near the ground state in Na$_3$Mn(CO$_3$)$_2$Cl is supported by the magnetic entropy estimated as almost 4 J K$^{-2}$ mol$^{-1}$ at 0.5 K.
We investigated magnetic and thermodynamic properties of $S$ = 1/2 quasi-one-dimensional antiferromagnet KCuMoO$_4$(OH) through single crystalline magnetization and heat capacity measurements. At zero field, it behaves as a uniform $S$ = 1/2 Heisenbe
rg antiferromagnet with $J$ = 238 K, and exhibits a canted antiferromagnetism below $T_mathrm{N}$ = 1.52 K. In addition, a magnetic field $H$ induces the anisotropy in magnetization and opens a gap in the spin excitation spectrum. These properties are understood in terms of an effective staggered field induced by staggered g-tensors and Dzyaloshinsky-Moriya (DM) interactions. Temperature-dependencies of the heat capacity and their field variations are consistent with those expected for quantum sine-Gordon model, indicating that spin excitations consist of soliton, anti-soliton and breather modes. From field-dependencies of the soliton mass, the staggered field normalized by the uniform field $c_mathrm{s}$ is estimated as 0.041, 0.174, and 0.030, for $H parallel a$, $b$, and $c$, respectively. Such a large variation of $c_mathrm{s}$ is understood as the combination of staggered g-tensors and DM interactions which induce the staggered field in the opposite direction for $H parallel a$ and $c$ but almost the same direction for $H parallel b$ at each Cu site.
We report on the electronic ground state of a layered perovskite vanadium oxide Sr$_2$VO$_4$ studied by the combined use of synchrotron radiation x-ray diffraction (SR-XRD) and muon spin rotation/relaxation ($mu$SR) techniques, where $mu$SR measureme
nts were extended down to 30 mK. We found an intermediate orthorhombic phase between $T_{rm c2} sim$~130 K and $T_{rm c1} sim$~100 K, whereas a tetragonal phase appears for $T > T_{rm c2}$ and $T < T_{rm c1}$. The absence of long-range magnetic order was confirmed by $mu$SR at the reentrant tetragonal phase below $T_{rm c1}$, where the relative enhancement in the $c$-axis length versus that of the $a$-axis length was observed. However, no clear indication of the lowering of the tetragonal lattice symmetry with superlattice modulation, which is expected in the orbital order state with superstructure of $d_{yz}$ and $d_{zx}$ orbitals, was observed by SR-XRD below $T_{rm c1}$. Instead, it was inferred from $mu$SR that a magnetic state developed below $T_{rm c0} sim$~10 K, which was characterized by the highly inhomogeneous and fluctuating local magnetic fields down to 30 mK. We argue that the anomalous magnetic ground state below $T_{rm c0}$ originates from the coexistence of ferromagnetic and antiferromagnetic correlations.
In a frustrated J_1-J_2 chain with the nearest-neighbor ferromagnetic interaction J_1 and the next-nearest-neighbor antiferromagnetic interaction J_2, novel magnetic states such as a spin-nematic state are theoretically expected. However, they have b
een rarely examined in experiments because of the difficulty in obtaining suitable model compounds. We show here that the quasi-one-dimensional antiferromagnet NaCuMoO_4(OH), which comprises edge-sharing CuO_2 chains, is a good candidate J_1-J_2 chain antiferromagnet. The exchange interactions are estimated as J_1 = - 51 K and J_2 = 36 K by comparing the magnetic susceptibility, heat capacity, and magnetization data with the data obtained using calculations by the exact diagonalization method. High-field magnetization measurements at 1.3 K show a saturation above 26 T with little evidence of a spin nematic state expected just below the saturation field, which is probably due to smearing effects caused by thermal fluctuations and the polycrystalline nature of the sample.
