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Register a new userRandom singlet state in Ba$_5$CuIr$_3$O$_{12}$ single crystals
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Added by
Pavel Volkov Andreevich
Publication date
2020
fields
Physics
and research's language is
English
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We study the thermodynamic and high-magnetic-field properties of the magnetic insulator Ba$_5$CuIr$_3$O$_{12}$, which shows no magnetic order down to 2 K consistent with a spin liquid ground state. While the temperature dependence of the magnetic susceptibility and the specific heat shows only weak antiferromagnetic correlations, we find that the magnetization does not saturate up to a field of 59 Tesla, leading to an apparent contradiction. We demonstrate that the paradox can be resolved, and all of the experimental data can be consistently described within the framework of random singlet states. We demonstrate a generic procedure to derive the exchange coupling distribution $P(J)$ from the magnetization measurements and use it to show that the experimental data is consistent with the power-law form $P(J)sim J^{-alpha}$ with $alpha approx 0.6 $. Thus, we reveal that high-magnetic-field measurements can be essential to discern quantum spin liquid candidates from disorder dominated states that do not exhibit long-range order.
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Terbium gallium garnet (TGG), Tb$_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.
Magnetic susceptibility and the magnetization process have been measured in green polycrystal. In this compound, the magnetic manganese ion exists as Mn$^{5+}$ in a tetrahedral environment, and thus the magnetic interaction can be described by an S=1 Heisenberg model. The ground state was found to be a spin singlet with an excitation gap $Delta/k_{rm B}=11.2$ K. Magnetization plateaus were observed at zero and at half of the saturation magnetization. These results indicate that the present system can be represented by a coupled antiferromagnetic dimer model.
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.
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.
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