اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدSpin-lozenge thermodynamics and magnetic excitations in Na$_3$RuO$_4$
98
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We report inelastic and elastic neutron scattering, magnetic susceptibility, and heat capacity measurements of polycrystalline sodium ruthenate (Na$_3$RuO$_4$). Previous work suggests this material consists of isolated tetramers of $S=3/2$ Ru$^{5+}$ ions in a so-called lozenge configuration. Using a Heisenberg antiferromagnet Hamiltonian, we analytically determine the energy eigenstates for general spin $S$. From this model, the neutron scattering cross-sections for excitations associated with spin-3/2 spin-tetramer configurations is determined. Comparison of magnetic susceptibility and inelastic neutron scattering results shows that the proposed lozenge model is not distinctly supported, but provides evidence that the system may be better described as a pair of non-interacting inequivalent dimers, textit{i.e} double dimers. However, the existence of long-range magnetic order below $T_c approx 28$ K immediately questions such a description. Although no evidence of the lozenge model is observed, future studies on single crystals may further clarify the appropriate magnetic Hamiltonian.
قيم البحث
اقرأ أيضاً
Magnetic properties and underlying magnetic models of the synthetic A$_2$Cu$_3$O(SO$_4)_3$ fedotovite (A = K) and puninite (A = Na) minerals, as well as the mixed euchlorine-type NaKCu$_3$O(SO$_4)_3$ are reported. We show that all these compounds con
tain magnetic Cu$_6$ hexamer units, which at temperatures below about 100 K act as single spin-1 entities. Weak interactions between these magnetic molecules lead to long-range order below $T_N$ = 3.4 K (A = Na), 4.7 K (A = NaK), and about 3.0 K (A = K). The formation of the magnetic order is elucidated by ab initio calculations that reveal two-dimensional inter-hexamer interactions within crystallographic $bc$ planes. This model indicates the presence of a weakly distorted square lattice of $S=1$ magnetic ions and challenges the earlier description of the A$_2$Cu$_3$O(SO$_4)_3$ minerals in terms of Haldane spin chains.
All-solid-state batteries using sodium are promising candidates for next-generation rechargeable batteries due to the limited lithium resources. A practical sodium battery requires an electrolyte with high conductivity. Cubic Na$_3$PS$_4$ exhibiting
high conductivity of over 10$^{-4}$ S cm$^{-1}$ is obtained by crystallizing amorphous Na$_3$PS$_4$ synthesized by ball milling. Amorphous Na$_3$PS$_4$ crystallizes in a cubic structure and then is transformed into a tetragonal phase upon heating. In this study, in situ observation by transmission electron microscopy demonstrates that the crystallite size drastically increases during the transition from the cubic phase to the tetragonal phase. Moreover, an electron diffraction analysis reveals that amorphous domains and nano-sized crystallites coexist in the cubic Na$_3$PS$_4$ specimen, while the tetragonal phase contains micro-sized crystallites. The nano-sized crystallites and the composite formed by crystallites and amorphous domains are most likely responsible for the increase in conductivity in the cubic Na$_3$PS$_4$ specimens.
Using a combination of density functional theory (DFT) and spin-wave theory methods, we investigate the magnetic interactions and spin excitations in semiconducting VI$_3$. Exchange parameters of monolayer, bilayer, and bulk forms are evaluated by ma
pping the magnetic energies of various spin configurations, calculated using DFT+$U$, onto the Heisenberg model. The intralayer couplings remain largely unchanged in three forms of VI$_3$, while the interlayer couplings show stronger dependence on the dimensionality of the materials. We calculate the spin-wave spectra within a linear spin-wave theory and discuss how various exchange parameters affect the magnon bands. The magnon-magnon interaction is further incorporated, and the Curie temperature is estimated using a self-consistently renormalized spin-wave theory. To understand the roles of constituent atoms on magnetocrystalline anisotropy energy (MAE), we resolve MAE into sublattices and find that a strong negative V-I inter-sublattice contribution is responsible for the relatively small easy-axis MAE in VI$_3$.
We use Ru $L_3$-edge (2838.5 eV) resonant inelastic x-ray scattering (RIXS) to quantify the electronic structure of Ca$_2$RuO$_4$, a layered $4d$-electron compound that exhibits a correlation-driven metal-insulator transition and unconventional antif
erromagnetism. We observe a series of Ru intra-ionic transitions whose energies and intensities are well described by model calculations. In particular, we find a $rm{J}=0rightarrow 2$ spin-orbit excitation at 320 meV, as well as Hunds-rule driven $rm{S}=1rightarrow 0$ spin-state transitions at 750 and 1000 meV. The energy of these three features uniquely determines the spin-orbit coupling, tetragonal crystal-field energy, and Hunds rule interaction. The parameters inferred from the RIXS spectra are in excellent agreement with the picture of excitonic magnetism that has been devised to explain the collective modes of the antiferromagnetic state. $L_3$-edge RIXS of Ru compounds and other $4d$-electron materials thus enables direct measurements of interactions parameters that are essential for realistic model calculations.
We report a combined experimental and theoretical investigation of the magnetic structure of the honeycomb lattice magnet Na$_2$IrO$_3$, a strong candidate for a realization of a gapless spin-liquid. Using resonant x-ray magnetic scattering at the Ir
L$_3$-edge, we find 3D long range antiferromagnetic order below T$_N$=13.3 K. From the azimuthal dependence of the magnetic Bragg peak, the ordered moment is determined to be predominantly along the {it a}-axis. Combining the experimental data with first principles calculations, we propose that the most likely spin structure is a novel zig-zag structure.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
