RESUMEN
Pyrochlore magnets have attracted interest as systems for realizing critical phenomena, rich magnetic structures, associated topological band structures, and nontrivial quantum phases. Na3Co(CO3)2Cl is a pseudospin-1/2 antiferromagnet in which the Co2+ions form a pyrochlore network. Its structural and magnetic properties were investigated using magnetization, heat capacity, ESR, single-crystal x-ray diffraction, powder neutron diffraction and powder inelastic neutron scattering. Magnetization and heat capacity measurements indicated a ground-state doublet, which is regarded as pseudospin 1/2, dominated the magnetic properties at low temperatures, with a magnetic exchange of 9.6 K. As the temperature decreases, a magnetic transition is observed at 1.6 K, which is confirmed to be an all-in-all-out magnetic order. The crystal field excitations observed by inelastic neutron scattering experiments indicated the Ising nature of the ground-state doublet. This thorough study revealed that Na3Co(CO3)2Cl can be regarded as a pseudospin-1/2 pyrochlore lattice antiferromagnet with dominant Ising-type interactions.
RESUMEN
The discovery of topological insulators and semimetals triggered enormous interest in exploring emergent electromagnetic responses in solids. Particular attention has been focused on ternary half-Heusler compounds, whose electronic structure bears analogy to the topological zinc-blende compounds while also including magnetic rare-earth ions coupled to conduction electrons. However, most of the research in this system has been in band-inverted zero-gap semiconductors such as GdPtBi, which still does not fully exhaust the large potential of this material class. Here, we report a less-studied member of half-Heusler compounds, HoAuSn, which we show is a trivial semimetal or narrow-gap semiconductor at zero magnetic field but undergoes a field-induced transition to a Weyl semimetal, with a negative magnetoresistance exceeding four orders of magnitude at low temperatures. The combined study of Shubnikov-de Haas oscillations and first-principles calculation suggests that the exchange field from Ho 4f moments reconstructs the band structure to induce Weyl points which play a key role in the strong suppression of large-angle carrier scattering. Our findings demonstrate the unique mechanism of colossal negative magnetoresistance and provide pathways towards realizing topological electronic states in a large class of magnetic half-Heusler compounds.
RESUMEN
Magnetic skyrmions are topologically stable swirling spin textures with particle-like character, and have been intensively studied as a candidate of high-density information bit. While magnetic skyrmions were originally discovered in noncentrosymmetric systems with Dzyaloshinskii-Moriya interaction, recently a nanometric skyrmion lattice has also been reported for centrosymmetric rare-earth compounds, such as Gd2PdSi3 and GdRu2Si2. For the latter systems, a distinct skyrmion formation mechanism mediated by itinerant electrons has been proposed, and the search of a simpler model system allowing for a better understanding of their intricate magnetic phase diagram is highly demanded. Here, we report the discovery of square and rhombic lattices of nanometric skyrmions in a centrosymmetric binary compound EuAl4, by performing small-angle neutron and resonant elastic X-ray scattering experiments. Unlike previously reported centrosymmetric skyrmion-hosting materials, EuAl4 shows multiple-step reorientation of the fundamental magnetic modulation vector as a function of magnetic field, probably reflecting a delicate balance of associated itinerant-electron-mediated interactions. The present results demonstrate that a variety of distinctive skyrmion orders can be derived even in a simple centrosymmetric binary compound, which highlights rare-earth intermetallic systems as a promising platform to realize/control the competition of multiple topological magnetic phases in a single material.
