اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدEvaluation of Exchange Interactions of the Spin Doughnut Mo_{75}V_{20}
115
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
Magnetic properties of the spin doughnut Mo_{75}V_{20}, which is a frustrated magnetic cluster with twenty spins, are studied by using the finite-temperature Lanczos method. Our model Hamiltonian consists of one ten-spin ring and two five-spin rings with nearest-neighbor antiferromagnetic couplings J and J. The five-spin rings are coupled to the ten-spin ring by an antiferromagnetic exchange interaction J so as to form isosceles triangles of one J-bond and two J-bonds. Fitting the theoretical magnetic susceptibility with the experimental one measured by Muller et al., the exchange parameters are estimated as J=388 K, J=163 K and J=81 K. The most interesting feature of this system is that the two five-spin rings behave like two free-spins at low temperatures in despite of J>J. We also calculate temperature dependence of the specific heat, and find three peaks at T sim J, J and J/100.
قيم البحث
اقرأ أيضاً
The spin-1/2 triangular lattice antiferromagnet YbMgGaO$_{4}$ has attracted recent attention as a quantum spin-liquid candidate with the possible presence of off-diagonal anisotropic exchange interactions induced by spin-orbit coupling. Whether a qua
ntum spin-liquid is stabilized or not depends on the interplay of various exchange interactions with chemical disorder that is inherent to the layered structure of the compound. We combine time-domain terahertz spectroscopy and inelastic neutron scattering measurements in the field polarized state of YbMgGaO$_{4}$ to obtain better microscopic insights on its exchange interactions. Terahertz spectroscopy in this fashion functions as high-field electron spin resonance and probes the spin-wave excitations at the Brillouin zone center, ideally complementing neutron scattering. A global spin-wave fit to all our spectroscopic data at fields over 4T, informed by the analysis of the terahertz spectroscopy linewidths, yields stringent constraints on $g$-factors and exchange interactions. Our results paint YbMgGaO$_{4}$ as an easy-plane XXZ antiferromagnet with the combined and necessary presence of sub-leading next-nearest neighbor and weak anisotropic off-diagonal nearest-neighbor interactions. Moreover, the obtained $g$-factors are substantially different from previous reports. This works establishes the hierarchy of exchange interactions in YbMgGaO$_{4}$ from high-field data alone and thus strongly constrains possible mechanisms responsible for the observed spin-liquid phenomenology.
Magnetism of transition metal (TM) oxides is usually described in terms of the Heisenberg model, with orientation-independent interactions between the spins. However, the applicability of such a model is not fully justified for TM oxides because spin
polarization of oxygen is usually ignored. In the conventional model based on the Anderson principle, oxygen effects are considered as a property of the TM ion and only TM interactions are relevant. Here, we perform a systematic comparison between two approaches for spin polarization on oxygen in typical TM oxides. To this end, we calculate the exchange interactions in NiO, MnO, and hematite (Fe2O3) for different magnetic configurations using the magnetic force theorem. We consider the full spin Hamiltonian including oxygen sites, and also derive an effective model where the spin polarization on oxygen renormalizes the exchange interactions between TM sites. Surprisingly, the exchange interactions in NiO depend on the magnetic state if spin polarization on oxygen is neglected, resulting in non-Heisenberg behavior. In contrast, the inclusion of spin polarization in NiO makes the Heisenberg model more applicable. Just the opposite, MnO behaves as a Heisenberg magnet when oxygen spin polarization is neglected, but shows strong non-Heisenberg effects when spin polarization on oxygen is included. In hematite, both models result in non-Heisenberg behavior. General applicability of the magnetic force theorem as well as the Heisenberg model to TM oxides is discussed.
We derive a set of equations expressing the parameters of the magnetic interactions characterizing a strongly correlated electronic system in terms of single-electron Greens functions and self-energies. This allows to establish a mapping between the
initial electronic system and a spin model including up to quadratic interactions between the effective spins, with a general interaction (exchange) tensor that accounts for anisotropic exchange, Dzyaloshinskii-Moriya interaction and other symmetric terms such as dipole-dipole interaction. We present the formulas in a format that can be used for computations via Dynamical Mean Field Theory algorithms.
We perform inelastic neutron scattering measurements on the molecular nanomagnet Mn_12-acetate to measure the excitation spectrum up to 45meV (500K). We isolate magnetic excitations in two groups at 5-6.5meV (60-75K) and 8-10.5meV (95-120K), with hig
her levels appearing only at 27meV (310K) and 31meV (360K). From a detailed characterization of the transition peaks we show that all of the low-energy modes appear to be separate S = 9 excitations above the S = 10 ground state, with the peak at 27meV (310K) corresponding to the first S = 11 excitation. We consider a general model for the four exchange interaction parameters of the molecule. The static susceptibility is computed by high-temperature series expansion and the energy spectrum, matrix elements and ground-state spin configuration by exact diagonalization. The theoretical results are matched with experimental observation by inclusion of cluster anisotropy parameters, revealing strong constraints on possible parameter sets. We conclude that only a model with dominant exchange couplings J_1 ~ J_2 ~ 5.5meV (65K) and small couplings J_3 ~ J_4 ~ 0.6meV (7K) is consistent with the experimental data.
The applicability of a broken symmetry version of the $G_0W_0$ approximation to the calculation of isotropic exchange coupling constants has been studied. Using a simple H--He--H model system the results show a significant and consistent improvement
of the results over both broken symmetry Hartree--Fock and broken symmetry density functional theory. In the case of more realistic bimetallic Cu(II) complexes, inclusion of the $G_0W_0$ correction does not lead to obvious improvement in the results. The discrepancies are explained by improved description of the interactions within the magnetic orbital space upon inclusion of the $G_0W_0$ corrections but deterioration of the description of charge- and spin-polarization effects outside the magnetic orbital space. Overall the results show that computational methods based on the $GW$ method have a potential to improve computational estimates of exchange coupling constants.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
