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Register a new userIsotropic and Anisotropic Regimes of the Field-Dependent Spin Dynamics in Sr2IrO4: Raman Scattering Studies
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A major focus of experimental interest in Sr2IrO4 has been to clarify how the magnetic excitations of this strongly spin-orbit coupled system differ from the predictions of anisotropic 2D spin-1/2 Heisenberg model and to explore the extent to which strong spin-orbit coupling affects the magnetic properties of iridates. Here, we present a high-resolution inelastic light (Raman) scattering study of the low energy magnetic excitation spectrum of Sr2IrO4 and doped Eu-doped Sr2IrO4 as functions of both temperature and applied magnetic field. We show that the high-field (H>1.5 T) in-plane spin dynamics of Sr2IrO4 are isotropic and governed by the interplay between the applied field and the small in-plane ferromagnetic spin components induced by the Dzyaloshinskii-Moriya interaction. However, the spin dynamics of Sr2IrO4 at lower fields (H<1.5 T) exhibit important effects associated with interlayer coupling and in-plane anisotropy, including a spin-flop transition at Hc in Sr2IrO4 that occurs either discontinuously or via a continuous rotation of the spins, depending upon the in-plane orientation of the applied field. These results show that in-plane anisotropy and interlayer coupling effects play important roles in the low-field magnetic and dynamical properties of Sr2IrO4.
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We have used Raman scattering to investigate the magnetic excitations and lattice dynamics in the prototypical spin-orbit Mott insulators Sr2IrO4 and Sr3Ir2O7. Both compounds exhibit pronounced two-magnon Raman scattering features with different energies, lineshapes, and temperature dependencies, which in part reflect the different influence of long-range frustrating exchange interactions. Additionally, we find strong Fano asymmetries in the lineshapes of low-energy phonon modes in both compounds, which disappear upon cooling below the antiferromagnetic ordering temperatures. These unusual phonon anomalies indicate that the spin-orbit coupling in Mott-insulating iridates is not sufficiently strong to quench the orbital dynamics in the paramagnetic state.
As a simple cubic system with only one f electron per cerium ion, CeB6 is of model character to investigate the interplay of orbital phenomena with magnetism. It is also a textbook example of a compound that exhibits magnetically hidden order -- a low-temperature magnetic phase with ordered quadrupolar moments. It is difficult to identify the symmetry of such hidden-order states in common x-ray or neutron scattering experiments, as there is no signal in zero field, however alternative techniques like neutron diffraction in external field, resonant x-ray scattering, or ultrasonic investigations can be applied. Another possible method for characterizing hidden order is to look at the magnetic excitation spectrum, which carries the imprint of the multipolar interactions and the hidden order parameter in its dispersion relations. Using a specific candidate model, the dispersion is calculated and then compared to that measured with inelastic neutron scattering. Until recently, only a limited amount of data which show the presence of dispersing excitations measured along a few high-symmetry directions in an applied magnetic field were available. Early attempts to compare such calculations with experiments showed that only strongest modes at high-symmetry points could be identified. The present review of the most recent neutron-scattering results is intended to satisfy the need of more accurate inelastic neutron-scattering experiments as a function of field and temperature, giving us the opportunity to identify existing excitation branches in CeB6 and conclusively compare them with the theoretically predicted multipolar excitations.
Strong spin-orbit interaction in the two dimensional compound Sr2IrO4 leads to the formation of Jeff=1/2 isospins with unprecedented dynamics. In Raman scattering a continuum attributed to double spin scattering is observed. With higher excitation energy of the incident Laser this signal crosses over to an incoherent background. The characteristic energy scale of this cross over is identical to that of intensity resonance effects in phonon scattering. It is related to exciton-like orbital excitations that are also evident in resonant X-Ray scattering. The crossover and evolution of incoherent excitations are proposed to be due to their coupling to spin excitations. This signals a spin-orbit induced entanglement of spin, lattice and charge degrees of freedoms in Sr2IrO4.
We develop a theory of the dynamical response of a minimal model of quantum spin ice (QSI) by means of inelastic light scattering. In particular, we are interested in the Raman response of the fractionalized U(1) spin liquid realized in the XXZ QSI. We show that the low-energy Raman intensity is dominated by spinon and gauge fluctuations. We find that the Raman response in the QSI state of that model appears only in the $T_{2g}$ polarization channel. We show that the Raman intensity profile displays a broad continuum from the spinons and coupled spinon and gauge fluctuations, and a low-energy peak arising entirely from gauge fluctuations. Both features originate from the exotic interaction between photon and the fractionalized excitations of QSI. Our theoretical results suggest that inelastic Raman scattering can in principle serve as a promising experimental probe of the nature of a U(1) spin liquid in QSI.
The ferrimagnetic spinel Mn3O4 exhibits large and anisotropic changes in electronic and structural properties in response to an applied magnetic field. These changes are thought to result from the field-dependent tuning---via strong spin-lattice coupling---between two nearly degenerate magnetostructural phases. Recent variable-magnetic-field studies of Mn3O4 have been performed on melt-grown crystals, which can exhibit twin domains due to a Jahn-Teller structural transition below the melting temperature. Because of the near degeneracy of the magnetostructural phases, however, strain associated with the twin domains likely affects the magnetic responses of Mn3O4. In this report, we present a variable-magnetic-field Raman scattering study of untwinned Mn3O4 crystals grown out of a flux below the Jahn-Teller structural transition. We measure distinct q = 0 magnetic and vibrational excitation spectra for each isolated magnetostructural phase of untwinned Mn3O4 crystals and determine the symmetries of the observed excitations. We determine how the magnetostructural phase mixture changes in response to magnetic fields applied in the magnetic easy plane. Lastly, by comparing results on flux- and melt-grown Mn3O4 crystals, we show that the intrinsic mixture of the two magnetostructural phases is indeed strongly influenced by the presence of twin domains.
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