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Register a new userCompeting Ferri- and Antiferromagnetic Phases in Geometrically Frustrated LuFe2O4
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We present a detailed study of magnetism in LuFe2O4, combining magnetization measurements with neutron and soft x-ray diffraction. The magnetic phase diagram in the vicinity of T_N involves a metamagnetic transition separating an antiferro- and a ferrimagnetic phase. For both phases the spin structure is refined by neutron diffraction. Observed diffuse magnetic scattering far above T_N is explained in terms of near degeneracy of the magnetic phases.
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The transmission electron microscopy observations of the charge ordering (CO) which governs the electronic polarization in LuFe2O4-x clearly show the presence of a remarkable phase separation at low temperatures. Two CO ground states are found to adopt the charge modulations of Q1 = (1/3, 1/3, 0) and Q2 = (1/3 + y, 1/3 + y, 3/2), respectively. Our structural study demonstrates that the incommensurately Q2-modulated state is chiefly stable in samples with relatively lower oxygen contents. Data from theoretical simulations of the diffraction suggest that both Q1- and Q2-modulated phases have ferroelectric ordering. The effects of oxygen concentration on the phase separation and electric polarization in this layered system are discussed.
The layered FeTe2O5Cl compound was studied by specific-heat, muon spin relaxation, nuclear magnetic resonance, dielectric, as well as neutron and synchrotron x-ray diffraction measurements, and the results were compared to isostructural FeTe2O5Br. We find that the low-temperature ordered state, similarly as in FeTe2O5Br, is multiferroic - the elliptical amplitude-modulated magnetic cycloid and the electric polarization simultaneously develop below 11 K. However, compared to FeTe2O5Br, the magnetic elliptical envelop rotates by 75(4) deg and the orientation of the electric polarization is much more sensitive to the applied electric field. We propose that the observed differences between the two isostructural compounds arise from geometric frustration, which enhances the effects of otherwise subtle Fe3+ (S = 5/2) magnetic anisotropies. Finally, x-ray diffraction results imply that, on the microscopic scale, the magnetoelectric coupling is driven by shifts of the O1 atoms, as a response to the polarization of the Te4+ lone-pair electrons involved in the Fe-O-Te-O-Fe exchange bridges.
In quantum spin systems, singlet phases often develop in the vicinity of an antiferromagnetic order. Typical settings for such problems arise when itinerant fermions are also present. In this work, we develop a theoretical framework for addressing such competing orders in an itinerant system, described by Dirac fermions strongly coupled to an O(3) nonlinear sigma model. We focus on two spatial dimensions, where upon disordering the antiferromagnetic order by quantum fluctuations the singular tunneling events also known as (anti)hedgehogs can nucleate competing singlet orders in the paramagnetic phase. In the presence of an isolated hedgehog configuration of the nonlinear sigma model field, we show that the fermion determinant vanishes as the dynamic Euclidean Dirac operator supports fermion zero modes of definite chirality. This provides a topological mechanism for suppressing the tunneling events. Using the methodology of quantum chromodynamics, we evaluate the fermion determinant in the close proximity of magnetic quantum phase transition, when the antiferromagnetic order parameter field can be described by a dilute gas of hedgehogs and antihedgehogs. We show how the precise nature of emergent singlet order is determined by the overlap between dynamic fermion zero modes of opposite chirality, localized on the hedgehogs and antihedgehogs. For a Kondo-Heisenberg model on the honeycomb lattice, we demonstrate the competition between spin Peierls order and Kondo singlet formation, thereby elucidating its global phase diagram. We also discuss other physical problems that can be addressed within this general framework.
We present a comprehensive review of nuclear magnetic resonance (NMR) studies performed on three nanoscale molecular magnets with different configurations of geometrically frustrated antiferromagnetic (AFM) triangles, new spin frustration systems with different novel structures: (1) the isolated single AFM triangle K$_6$[V$_{15}$As$_6$O$_{42}$(H$_2$O)]$cdot$8H$_2$O (in short V15), (2) the spin ball [Mo$_{72}$Fe$_{30}$O$_{252}$(Mo$_2$O$_7$(H$_2$O))$_2$ (Mo$_2$O$_8$H$_2$(H$_2$O))(CH$_3$COO)$_{12}$(H$_2$O)$_{91}$]$cdot$150H$_2$O (in short Fe30 spin ball), and (3) the twisted triangular spin tube [(CuCl$_2$tachH)$_3$Cl]Cl$_2$ (in short Cu3 spin tube).
The nature of the low temperature ground state of the pyrochlore compound Tb2Ti2O7 remains a puzzling issue. Dynamic fluctuations and short-range correlations persist down to 50 mK, as evidenced by microscopic probes. In parallel, magnetization measurements show irreversibilities and glassy behavior below 200 mK. We have performed magnetization and AC susceptibility measurements on four single crystals down to 57 mK. We did not observe a clear plateau in the magnetization as a function of field along the [111] direction, as suggested by the quantum spin ice model. In addition to a freezing around 200 mK, slow dynamics are observed in the AC susceptibility up to 4 K. The overall frequency dependence cannot be described by a canonical spin-glass behavior.
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