No Arabic abstract
We report magnetic susceptibility, specific heat and muon spin relaxation (muSR) experiments on the triangular antiferromagnet La2Ca2MnO7 which develops a genuine two-dimensional, three-sublattice sqrt{3} times sqrt{3} magnetic order below T_N = 2.8 K. From the susceptibility and specific heat data an estimate of the exchange interaction is derived. A value for the spin-wave gap is obtained from the latter data. The analysis of a previously reported inelastic neutron scattering study yields values for the exchange and spin-wave gap compatible with the results obtained from macroscopic measurements. An appreciable entropy is still missing at 10 K that may be ascribed to intense short-range correlations. The critical paramagnetic fluctuations extend far above T_N, and can be partly understood in terms of two-dimensional spin-wave excitations. While no spontaneous muSR field is observed below T_N, persistent spin dynamics is found. Short-range correlations are detected in this temperature range. Their relation to a possible molecular spin substructure and the observed exotic spin fluctuations is discussed.
We report a spin S = 3/2 triangular antiferromagnet with nearest-neighbor coupling J = 0.29 meV in La2Ca2MnO7. A genuinely two-dimensional, three-sublattice order develops below 2.80 K << the Weiss constant (25 K). The spin excitations deviate substantially from linear spin-wave theory, suggesting that magnon breakdown occurs in the material. Such a breakdown has been anticipated in recent theoretical studies, although the excitation spectrum remains to be accounted for.
We have investigated the spin fluctuations in the langasite compound Ba3NbFe3Si2O14 in both the ordered state and as a function of temperature. The low temperature magnetic structure is defined by a spiral phase characterized by magnetic Bragg peaks at q=(0,0,tau ~ 1/7) onset at TN=27 K as previously reported by Marty et al. The nature of the fluctuations and temperature dependence of the order parameter is consistent with a classical second order phase transition for a two dimensional triangular antiferromagnet. We will show that the physical properties and energy scales including the ordering wavevector, Curie-Weiss temperature, and the spin-waves can be explained through the use of only symmetric exchange constants without the need for the Dzyaloshinskii-Moriya interaction. This is accomplished through a set of ``helical exchange pathways along the c direction imposed by the chiral crystal structure and naturally explains the magnetic diffuse scattering which displays a strong vector chirality up to high temperatures well above the ordering temperature. This illustrates a strong coupling between magnetic and crystalline chirality in this compound.
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.
We report a high-resolution neutron diffraction study of the crystal and magnetic structure of the orbitally-degenerate frustrated metallic magnet AgNiO2. At high temperatures the structure is hexagonal with a single crystallographic Ni site, low-spin Ni3+ with spin-1/2 and two-fold orbital degeneracy, arranged in an antiferromagnetic triangular lattice with frustrated spin and orbital order. A structural transition occurs upon cooling below 365 K to a tripled hexagonal unit cell containing three crystallographically-distinct Ni sites with expanded and contracted NiO6 octahedra, naturally explained by spontaneous charge order on the Ni triangular layers. No Jahn-Teller distortions occur, suggesting that charge order occurs in order to lift the orbital degeneracy. Symmetry analysis of the inferred Ni charge order pattern and the observed oxygen displacement pattern suggests that the transition could be mediated by charge fluctuations at the Ni sites coupled to a soft oxygen optical phonon breathing mode. At low temperatures the electron-rich Ni sublattice (assigned to a valence close to Ni2+ with S = 1) orders magnetically into a collinear stripe structure of ferromagnetic rows ordered antiferromagnetically in the triangular planes. We discuss the stability of this uncommon spin order pattern in the context of an easy-axis triangular antiferromagnet with additional weak second neighbor interactions and interlayer couplings.
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.