No Arabic abstract
Magnetic transition phenomena in cubic chiral antiferromagnet EuPtSi with $T_{rm N}$=4.0~K were investigated by means of single crystal neutron diffraction. At 0.3~K in the ground state, magnetic peaks emerge at positions represented by an ordering vector ${q}_{1}$=$(0.2, 0.3, 0)$ and its cyclic permutation. Upon heating, an additional magnetic peak splitting with hysteresis was uncovered at around $T^*_{rm N}{sim}$2.5~K, indicating the presence of a first-order commensurate-incommensurate transition with ${q}^*_{1}$=$(0.2, 0.3, {delta})$ (${delta}_{rm max}{simeq}$0.04) at $T^*_{rm N}$. A half-polarized neutron scattering experiment for polarization parallel to the scattering vector revealed that polarization antiparallel to the scattering vector has stronger intensity in both magnetic phases. This feature clarifies the single chiral character of the helical structure with moments lying perpendicular to the ordering vector in both ordered states. Under a vertical magnetic field of 1.2~T for ${B}{parallel}$[1,1,1] at 1.9~K entering into the so-called $A$ phase, magnetic peaks form characteristic hexagonal patterns in the equatorial scattering plane around nuclear peaks. An ordering vector ${q}_{A}{simeq}({pm}0.09, {pm}0.20, {mp}0.28)$ of the $A$-phase has similar periodic length as $q_{1}$, and could be the hallmark of a formation of skyrmion lattice in EuPtSi.
{alpha}-CaCr2O4 is a distorted triangular antiferromagnet. The magnetic Cr3+ ions which have spin-3/2 and interact with their nearest neighbors via Heisenberg direct exchange interactions, develop long-range magnetic order below T_N=42.6 K. Powder and single-crystal neutron diffraction reveal a helical magnetic structure with ordering wavevector k=(0,~1/3,0) and angles close to 120{deg} between neighboring spins. Spherical neutron polarimetry unambiguously proves that the spins lie in the ac plane perpendicular to k. The magnetic structure is therefore that expected for an ideal triangular antiferromagnet where all nearest neighbor interactions are equal, in spite of the fact that {alpha}-CaCr2O4 is distorted with two inequivalent Cr3+ ions and four different nearest neighbor interactions. By simulating the magnetic order as a function of these four interactions it is found that the special pattern of interactions in {alpha}-CaCr2O4 stabilizes 120{deg} helical order for a large range of exchange interactions.
High resolution time-of-flight neutron scattering measurements on Tb2Ti2O7 reveal a rich low temperature phase diagram in the presence of a magnetic field applied along [110]. In zero field at T=0.4 K, terbium titanate is a highly correlated cooperative paramagnet with disordered spins residing on a pyrochlore lattice of corner-sharing tetrahedra. Application of a small field condenses much of the magnetic diffuse scattering, characteristic of the disordered spins, into a new Bragg peak characteristic of a polarized paramagnet. At higher fields, a magnetically ordered phase is induced, which supports spin wave excitations indicative of continuous, rather than Ising-like spin degrees of freedom.
Taking the pseudobinary C15-Laves phase compound Ce(Fe$_{0.96}$Al$_{0.04}$)$_2$ as a paradigm for studying a ferromagnetic(FM) to antiferromagnetic(AFM) phase transition, we present interesting thermomagnetic history effects in magnetotransport measurements across this FM-AFM transition. We argue that these distinctive hysteretic features can be used to identify the exact nature -first order or second order - of this kind of transition in magnetic systems where electrical transport is strongly correlated with the underlying magnetic order. A comparison is made with the similar FM-AFM transitions observed in Nd and Pr-based manganese compounds with perovskite-type structure.
The thermal properties of antiferromagnetic films -- in particular, the square-lattice antiferromagnet -- subjected to an external magnetic field pointing into the direction of the staggered magnetization are explored. The effective field theory analysis of the free energy density is carried out to two-loop order. While the emphasis is on finite temperature, we also discuss the behavior of the magnetization and staggered magnetization at zero temperature. Our results imply that the staggered magnetization increases in presence of the magnetic field -- reminiscent of magnetic catalysis. Most remarkably, if staggered and magnetic field strength are kept fixed, the magnetization initially grows when temperature increases.
Yb- and Ce-based delafossites were recently identified as effective spin-1/2 antiferromagnets on the triangular lattice. Several Yb-based systems, such as NaYbO2, NaYbS2, and NaYbSe2, exhibit no long-range order down to the lowest measured temperatures and therefore serve as putative candidates for the realization of a quantum spin liquid. However, their isostructural Ce-based counterpart KCeS2 exhibits magnetic order below TN = 400 mK, which was so far identified only in thermodynamic measurements. Here we reveal the magnetic structure of this long-range ordered phase using magnetic neutron diffraction. We show that it represents the so-called stripe-yz type of antiferromagnetic order with spins lying approximately in the triangular-lattice planes orthogonal to the nearest-neighbor Ce-Ce bonds. No structural lattice distortions are revealed below TN, indicating that the triangular lattice of Ce3+ ions remains geometrically perfect down to the lowest temperatures. We propose an effective Hamiltonian for KCeS2, based on a fit to the results of ab initio calculations, and demonstrate that its magnetic ground state matches the experimental spin structure.