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Register a new userPartial ferromagnetic ordering and indirect exchange interaction in spatially anisotropic kagome antiferromagnet Cs_2Cu_3CeF_{12}
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We report the crystal structure and unconventional magnetic ordering of Cs_2Cu_3CeF_{12}, which is composed of buckled kagome lattice of Cu^{2+} ions. The exchange network in the buckled kagome lattice is fairly anisotropic, so that the present spin system can be divided into two subsystems: alternating Heisenberg chains with strong antiferromagnetic exchange interactions and dangling spins. Although the direct exchange interactions between neighboring spins were found to be all antiferromagnetic, ferromagnetic magnetic ordering of the dangling spins was observed. Magnetization exhibits a plateau at one-third of the saturation magnetization. These observations can be understood in terms of the indirect interaction between dangling spins mediated by the chain spin.
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In the search for spin-1/2 kagome antiferromagnets, the mineral volborthite has recently been the subject of experimental studies [Hiroi et al.,2001]. It has been suggested that the magnetic properties of this material are described by a spin-1/2 Heisenberg model on the kagome lattice with spatially anisotropic exchange couplings. We report on investigations of the Sp(N) symmetric generalisation of this model in the large N limit. We obtain a detailed description of the dependence of possible ground states on the anisotropy and on the spin length S. A fairly rich phase diagram with a ferrimagnetic phase, incommensurate phases with and without long range order and a decoupled chain phase emerges.
We have performed time-resolved resonant x-ray scattering studies in the Lanthanide metal Dy to reveal the dynamic response of the helical order exchange coupling to injection of unpolarized spins. The observed spin dynamics are significantly slower than that exhibited by the ferromagnetic phase in Lanthanide metals and are strongly dependent on temperature and excitation fluence. This unique behavior results from transient changes in the shape of the conduction electron Fermi surface and subsequent scattering events that transfer the excitation to the core spin.
We study the properties of the Heisenberg antiferromagnet with spatially anisotropic nearest-neighbour exchange couplings on the kagome net, i.e. with coupling J in one lattice direction and couplings J along the other two directions. For J/J > 1, this model is believed to describe the magnetic properties of the mineral volborthite. In the classical limit, it exhibits two kinds of ground states: a ferrimagnetic state for J/J < 1/2 and a large manifold of canted spin states for J/J > 1/2. To include quantum effects self-consistently, we investigate the Sp(N) symmetric generalisation of the original SU(2) symmetric model in the large-N limit. In addition to the dependence on the anisotropy, the Sp(N) symmetric model depends on a parameter kappa that measures the importance of quantum effects. Our numerical calculations reveal that in the kappa-J/J plane, the system shows a rich phase diagram containing a ferrimagnetic phase, an incommensurate phase, and a decoupled chain phase, the latter two with short- and long-range order. We corroborate these results by showing that the boundaries between the various phases and several other features of the Sp(N) phase diagram can be determined by analytical calculations. Finally, the application of a block-spin perturbation expansion to the trimerised version of the original spin-1/2 model leads us to suggest that in the limit of strong anisotropy, J/J >> 1, the ground state of the original model is a collinearly ordered antiferromagnet, which is separated from the incommensurate state by a quantum phase transition.
The ground state of the simple Heisenberg nearest-neighbor quantum kagome antiferromagnetic model is a magnetically disordered spin liquid, yet various perturbations may lead to fundamentally different states. Here we disclose the origin of magnetic ordering in the structurally-perfect kagome material YCu$_3$(OH)$_6$Cl$_3$, which is free of the widespread impurity problem. {it Ab-initio} calculations and modeling of its magnetic susceptibility reveal that, similar to the archetypal case of herbertsmithite, the nearest-neighbor exchange is by far the dominant isotropic interaction. Dzyaloshinskii-Moriya (DM) magnetic anisotropy deduced from electron spin resonance and specific-heat measurements is, however, significantly larger than in herbertsmithite. By enhancing spin correlations within kagome planes, this anisotropy is essential for magnetic ordering. Our study isolates the effect of DM anisotropy from other perturbations and unambiguously confirms the theoretical phase diagram.
In doped manganites, the strong electron-phonon coupling due to the Jahn-Teller effect localizes the conduction-band electrons as polarons. This results in polarons are carriers responsible for transport and ferromagnetic ordering rather than the bare eg electrons, and sequentially polaron exchange model is emerged for describing ferromagnetic ordering. In Pr0.7(Sr1-xCax)0.3MnO3(x=0.3-0.6) epitaxial thin films, for higher-temperature paramagnetic state and lower-temperature ferromagnetic state, both the temperature dependent transports present behaviors of small polaron; for paramagnetic-ferromagnetic transition, the experimental data of Curie temperature are well described by an energy balance expression induced by polaron exchange model. These results demonstrate that the polaron models are proper ways to describe the strongly correlated electrons in the doped manganites.
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