RESUMEN
Rare-earth (RE)-based honeycomb-lattice materials with strong spin-orbit coupled Jeff = 1/2 moments have attracted great interest as a platform to realize the Kitaev quantum spin liquid (QSL) state. Herein, we report the discovery of a family of RE-based honeycomb-lattice magnets Ba9RE2(SiO4)6 (RE = Ho-Yb), which crystallize into the rhombohedral structure with the space group R3Ì . In these serial compounds, magnetic RE3+ ions are arranged on a perfect honeycomb lattice within the ab-plane and stacked in the "ABCABC"-type fashion along the c-axis. All synthesized Ba9RE2(SiO4)6 (RE = Ho-Yb) polycrystals exhibit the dominant antiferromagnetic interaction and absence of magnetic order down to 2 K. In combination with the magnetization and electron spin resonance results, magnetic behaviors are discussed for the compounds with different RE ions. Moreover, the as-grown Ba9Yb2(SiO4)6 single crystals show large magnetic frustration with frustration index f = θCW/TN > 8 and no long-range magnetic ordering down to 0.15 K, being a possible QSL candidate material. These series of compounds are attractive for exploring the exotic magnetic phases of Kitaev materials with 4f electrons.
RESUMEN
Monoclinic Li3Co2SbO6 has been proposed as a Kitaev spin liquid candidate and investigated intensively, whereas the properties of its polymorph, the orthorhombic phase, are less known. Here we report the magnetic properties of orthorhombic Li3Co2SbO6 as revealed by dc and ac magnetic susceptibility, muon spin relaxation (µSR), and neutron diffraction measurements. Successive magnetic transitions at 115, 89, and 71 K were observed in the low-field dc susceptibility measurements. The transitions below TN (115 K) are suppressed at higher applied fields. However, zero-field ac susceptibility measurements reveal distinct frequency-independent transitions at about 114, 107, 97, 79, and 71 K. A long-range magnetic ordered state was confirmed by specific heat, µSR, and neutron diffraction measurements, all indicating a single transition at about 115 K. The discrepancy between different measurements is attributed to possible stacking faults and/or local disorders of the ferromagnetic zigzag chains, resulting in ferromagnetic boundaries within the overall antiferromagnetic matrix.
RESUMEN
In this work, strontium diazenide (SrN2) was synthesized using strontium azide as a starting material in a Walker-type module under high-pressure and high-temperature conditions. The synthesized SrN2 was further studied under high pressure up to 43.2 GPa using in situ synchrotron X-ray diffraction to supplement the high-pressure exploration of alkaline earth diazenides. The SrN2 underwent a possible phase transition from a tetragonal structure into an orthorhombic structure at 12.0 GPa. SrN2 shows anisotropic compressibility due to the orientation of the diazenide anions. The bulk modulus of SrN2 is 132.4 (10.2) GPa, which is larger than that of Sr(N3)2. The larger bulk modulus of SrN2 is attributed to the stronger covalent strength between Sr and N atoms in SrN2, which is confirmed by our theoretical calculations.