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Register a new userEmergent magnetic behaviour in the frustrated Yb$_3$Ga$_5$O$_{12}$ garnet
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We report neutron scattering, magnetic susceptibility and Monte Carlo theoretical analysis to verify the short range nature of the magnetic structure and spin-spin correlations in a Yb$_3$Ga$_5$O$_{12}$ single crystal. The quantum spin state of Yb$^{3+}$ in Yb$_3$Ga$_5$O$_{12}$ is verified. The quantum spins organise into a short ranged emergent director state for T $<$ 0.4 K derived from anisotropy and near neighbour exchange. We derive the magnitude of the near neighbour exchange interactions $0.6; {rm K} < J_1 < 0.7; {rm K}, J_2 = 0.12$~K and the magnitude of the dipolar exchange interaction, $D$, in the range $0.18 < D < 0.21$ K. Certain aspects of the broad experimental dataset can be modelled using a $J_1D$ model with ferromagnetic near neighbour spin-spin correlations while other aspects of the data can be accurately reproduced using a $J_1J_2D$ model with antiferromagnetic near neighbour spin-spin correlation. As such, although we do not quantify all the relevant exchange interactions we nevertheless provide a strong basis for the understanding of the complex Hamiltonian required to fully describe the magnetic state of Yb$_3$Ga$_5$O$_{12}$.
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We investigate ytterbium gallium garnet Yb$_{3}$Ga$_{5}$O$_{12}$ in the paramagnetic phase above the supposed magnetic transition at $T_{lambda} approx 54$ mK. Our study combines susceptibility and specific heat measurements with neutron scattering experiments and theoretical calculations. Below 500 mK, the elastic neutron response is strongly peaked in the momentum space. Along with that the inelastic spectrum develops flat excitation modes. In magnetic field, the lowest energy branch follows a Zeeman shift in accordance with the field-dependent specific heat data. An intermediate state with spin canting away from the field direction is evidenced in small magnetic fields. In the field of 2 T, the total magnetization almost saturates and the measured excitation spectrum is well reproduced by the spin-wave calculations taking into account solely the dipole-dipole interactions. The small positive Curie-Weiss temperature derived from the susceptibility measurements is also accounted for by the dipole spin model. Altogether, our results suggest that Yb$_{3}$Ga$_{5}$O$_{12}$ is a quantum dipolar magnet.
The transverse acoustic wave propagating along the [100] axis of the cubic Tb$_3$Ga$_5$O$_{12}$ (acoustic $c_{44}$ mode) is doubly degenerate. A magnetic field applied in the direction of propagation lifts this degeneracy and leads to the rotation of the polarization vector - the magneto-acoustic Faraday rotation. Here, we report on the observation and analysis of the magneto-acoustic Faraday-effect in Tb$_3$Ga$_5$O$_{12}$ in static and pulsed magnetic fields. We present also a theoretical model based on magnetoelastic coupling of 4$f$ electrons to both, acoustic and optical phonons and an effective coupling between them. This model explains the observed linear frequency dependence of the Faraday rotation angle.
Terbium gallium garnet (TGG), Tb$_3$Ga$_5$O$_{12}$, is well known for its applications in laser optics, but also exhibits complex low-temperature magnetism that is not yet fully understood. Its low-temperature magnetic order is determined by means of time-of-flight neutron powder diffraction. It is found to be a multiaxial antiferromagnet with magnetic Tb$^{3+}$ ions forming six sublattices of magnetic moments aligned parallel and anti-parallel to the $langle100rangle$ crystallographic directions of the cubic unit cell. The structure displays strong easy-axis anisotropy with respect to a two-fold axis of symmetry in the local orthorhombic environment of the Tb$^{3+}$ sites. The crystal-field splitting within the single-ion ground-state manifold is investigated by inelastic neutron scattering on powder samples. A strong temperature dependence of the quasidoublet ground-state is observed and revised parameters of the crystal-field Hamiltonian are given. The results of bulk magnetic susceptibility and magnetisation measurements are in good agreement with values based on the crystal-field model down to 20~K, where the onset of magnetic correlations is observed.
Ferrimagnetic Y$_3$Fe$_5$O$_{12}$ (YIG) is the prototypical material for studying magnonic properties due to its exceptionally low damping. By substituting the yttrium with other rare earth elements that have a net magnetic moment, we can introduce an additional spin degree of freedom. Here, we study the magnetic coupling in epitaxial Y$_3$Fe$_5$O$_{12}$/Gd$_3$Fe$_5$O$_{12}$ (YIG/GIG) heterostructures grown by pulsed laser deposition. From bulk sensitive magnetometry and surface sensitive spin Seebeck effect (SSE) and spin Hall magnetoresistance (SMR) measurements, we determine the alignment of the heterostructure magnetization through temperature and external magnetic field. The ferromagnetic coupling between the Fe sublattices of YIG and GIG dominates the overall behavior of the heterostructures. Due to the temperature dependent gadolinium moment, a magnetic compensation point of the total bilayer system can be identified. This compensation point shifts to lower temperatures with increasing thickness of YIG due the parallel alignment of the iron moments. We show that we can control the magnetic properties of the heterostructures by tuning the thickness of the individual layers, opening up a large playground for magnonic devices based on coupled magnetic insulators. These devices could potentially control the magnon transport analogously to electron transport in giant magnetoresistive devices.
The N$acute{rm e}$el temperature of the new frustrated family of Sremph{RE}$_2$O$_4$ (emph{RE} = rare earth) compounds is yet limited to $sim$ 0.9 K, which more or less hampers a complete understanding of the relevant magnetic frustrations and spin interactions. Here we report on a new frustrated member to the family, SrTb$_2$O$_4$ with a record $T_{rm N}$ = 4.28(2) K, and an experimental study of the magnetic interacting and frustrating mechanisms by polarized and unpolarized neutron scattering. The compound SrTb$_2$O$_4$ displays an incommensurate antiferromagnetic (AFM) order with a transverse wave vector textbf{Q}$^{rm 0.5 K}_{rm AFM}$ = (0.5924(1), 0.0059(1), 0) albeit with partially-ordered moments, 1.92(6) $mu_{rm B}$ at 0.5 K, stemming from only one of the two inequivalent Tb sites mainly by virtue of their different octahedral distortions. The localized moments are confined to the emph{bc} plane, 11.9(66)$^circ$ away from the emph{b} axis probably by single-ion anisotropy. We reveal that this AFM order is dominated mainly by dipole-dipole interactions and disclose that the octahedral distortion, nearest-neighbour (NN) ferromagnetic (FM) arrangement, different next NN FM and AFM configurations, and in-plane anisotropic spin correlations are vital to the magnetic structure and associated multiple frustrations. The discovery of the thus far highest AFM transition temperature renders SrTb$_2$O$_4$ a new friendly frustrated platform in the family for exploring the nature of magnetic interactions and frustrations.
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