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Danielle Yahne

Publications and source records attributed to Danielle Yahne.

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Pressure-Stabilized MnSb$_2$ with Complex Incommensurate Magnetic Order

Marcasite-type compounds have been proposed as promising hosts of exotic magnetic quantum states, yet experimental realizations in stoichiometric, disorder-free systems remain limited. Here, we report the high-pressure stabilization and magnetic characterization of MnSb$_2$, a marcasite-type compound that is thermodynamically metastable under ambient pressure. Single crystals were synthesized using a cubic multi-anvil press, and powder and single-crystal X-ray diffraction confirm the orthorhombic $Pnnm$ structure. These crystals are stable at ambient pressure for a long time up to between 450-500 K. Heat-capacity measurements reveal phase transitions at approximately 220 K and 118 K. Neutron diffraction uncovers an unconventional magnetic ground state below 220 K. Magnetic powder neutron diffraction refinements reveal possible multiple magnetic configurations that provide comparably acceptable fits to the experimental data. While most solutions are consistent with a spin-density-wave (SDW) description, helical models systematically yield inferior agreement factors. Across a broad range of models, the Mn ordered moment reaches a maximum value of approximately 2 $\mu_B$ and remains predominantly collinear, with minimal canting along the $c$-axis. At 200 K, the magnetic propagation vector is $q$ = (0, 0.3975, 0.3783); upon cooling, the $b$ component increases toward 0.5, reflecting a temperature-dependent evolution of the modulation. The need for modification of the magnetic model between high and low temperatures further highlights the complex and strongly temperature-dependent nature of the magnetic order in this system. These results establish MnSb$_2$ as a pressure-stabilized marcasite magnet with a highly tunable, complex magnetic ground state and a compelling stoichiometric platform for exploring unconventional magnetic behavior, including potential altermagnetism.

cond-mat.str-el

Jeff = 1/2 Diamond Magnet CaCo2TeO6: A Pathway toward New Spin Physics and Quantum Functions

Diamond lattice magnets, formed by a framework of corner-sharing tetrahedra of magnetic cations, offer unique opportunities to realize novel states of matter for potential utility in information technology. However, research has mostly focused on AB2X4 spinels with Td magnetic ions. This hinders the atomically enabled tunability of competing interactions at different energy scales and the ability to harness many-body electronic states in quantum materials, making the discovery of quantum fluctuations and spin dynamics less accessible. We discover a new material CaCo2TeO6 featuring a diamond lattice of two distinct Oh-Co2+ sites. This material displays strong quantum fluctuations, increased competing magnetic exchange interactions, and field-induced tunability of magnetic structures. The results demonstrate how simple, fundamental refinements in ligand fields can profoundly influence the phase space of quantum matter.

cond-mat.mtrl-sci