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Novel quantum materials offer the opportunity to expand next-generation computers, high-precision sensors, and new energy technologies. Among the most important factors influencing the development of quantum materials research is the ability of inorganic and materials chemists to grow high-quality single crystals. Here, the synthesis, structure characterization and magnetic properties of Na2Cu3(SeO3)4 are reported. It exhibits a novel two-dimensional (2D) structure with isolated layers of Cu nets. Single crystals of Na2Cu3(SeO3)4 were grown using a low-temperature hydrothermal method. Single-crystal X-ray diffraction reveals that Na2Cu3(SeO3)4 crystallizes in the monoclinic crystal system and has space group symmetry of P21/n (No.14) with a unit cell of a = 8.1704(4) Å, b = 5.1659(2) Å, c = 14.7406(6) Å, β = 100.86(2), V = 611.01(5) Å3 and Z = 2. Na2Cu3(SeO3)4 comprises a 2D Cu-O-Cu lattice containing two unique copper sites, a CuO6 octahedra and a CuO5 square pyramid. The SeO3 groups bridge the 2D Cu-O-Cu layers isolating the neighboring Cu-O-Cu layers, thereby enhancing their 2D nature. Magnetic properties were determined by measuring the magnetic susceptibility of an array of randomly oriented single crystals of Na2Cu3(SeO3)4. The temperature-dependent magnetic measurement shows an antiferromagnetic transition at TN = 4 K. These results suggest the fruitfulness of hydrothermal synthesis in achieving novel quantum materials and encourage future work on the chemistry of transition metal selenite. 

Single crystals of a new transition metal adelite-descloizite-type structure were synthesized using a high temperature (580 °C) high-pressure hydrothermal technique. Single crystal X-ray diffraction and energy dispersive X-ray analysis (EDX) were used to investigate the structure and elemental composition, respectively. SrNi(VO4)(OH) crystallizes in an acentric orthorhombic crystal system in the space group P212121 (no. 19); Z = 4, a = 5.9952(4) Å, b = 7.5844(4) Å, c = 9.2240(5) Å. The structure is comprised of a Ni–O–V framework where Sr2+ ions reside inside the channels. Single-crystal magnetic measurements display a significant anisotropy in both temperature- and field-dependent data. The temperature dependent magnetic measurement shows antiferromagnetic behavior at TN~8 K. Overall, the magnetic properties indicate the presence of competing antiferromagnetic and ferromagnetic interactions of SrNi(VO4)(OH). 

Abstract Topological kagome magnets RMn₆Sn₆(R = rare earth element) attract numerous interests due to their non-trivial band topology and room-temperature magnetism. Here, we report a high entropy version of kagome magnet, (Gd_0.38Tb_0.27Dy_0.20Ho_0.15)Mn₆Sn₆. Such a high entropy material exhibits multiple spin reorientation transitions, which is not seen in all the related parent compounds and can be understood in terms of competing magnetic interactions enabled by high entropy. Furthermore, we also observed an intrinsic anomalous Hall effect, indicating that the high entropy phase preserves the non-trivial band topology. These results suggest that high entropy may provide a route to engineer the magnetic structure and expand the horizon of topological materials.