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M. J. P. Gingras

Publications and source records attributed to M. J. P. Gingras.

48 records · Page 3Linked to original sources

Magnetic anisotropy of the spin ice compound Dy2Ti2O7

We report magnetization and ac susceptibility of single crystals of the spin ice compound Dy2Ti2O7. Saturated moments at 1.8 K along the charasteristic axes [100] and [110] agree with the expected values for an effective ferromagnetic nearest-neighbor Ising pyrochlore with local <111> anisotropy, where each magnetic moment is constrained to obey the `ice-rule'. At high enough magnetic fields along the [111] axis, the saturated moment exhibits a beaking of the ice-rule; it agrees with the value expected for a three-in one-out spin configuration. Assuming the realistic magnetic interaction between Dy ions given by the dipolar spin ice model, we completely reproduce the results at 2 K by Monte Carlo calculations. However, down to at least 60 mK, we have not found any experimental evidence of the long-range magnetic ordering predicted by this model to occur at around 180 mK. Instead, we confirm the spin freezing of the system below 0.5 K.

cond-mat.str-el↗

Spin Correlations in Ho$_{2}$Ti$_{2}$O$_{7}$: a Dipolar Spin Ice System

The pyrochlore material $\rm Ho_{2}Ti_{2}O_{7}$ has been suggested to show ``spin ice'' behaviour. We present neutron scattering and specific heat results that establish unambiguously that Ho$_2$Ti$_2$O$_7$ exhibits spin ice correlations at low temperature. Diffuse magnetic neutron scattering from Ho$_2$Ti$_2$O$_7$ is found to be quite well described by a near neighbour spin ice model and very accurately described by a dipolar spin ice model. The heat capacity is well accounted for by the sum of a dipolar spin ice contribution and an expected nuclear spin contribution, known to exist in other Ho$^{3+}$ salts. These results settle the question of the nature of the low temperature spin correlations in $\rm Ho_{2}Ti_{2}O_{7}$ for which contradictory claims have been made.

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Frustrated Order by Disorder: the Pyrochlore Antiferromagnet with Bond Disorder

The classical Heisenberg antiferromagnet on the pyrochlore lattice is macroscopically and continuously degenerate and the system remains disordered at all temperatures, even in the presence of weak dilution with nonmagnetic ions. We show that, in stark contrast, weak bond disorder lifts the ground state degeneracy in favour of locally collinear spin configurations. We present a proof that for a single tetrahedron the ground state is perfectly collinear but identify two mechanisms which preclude the establishment of a globally collinear state; one due to frustration and the other due to higher-order effects. We thus obtain a rugged energy landscape, which is necessary to account for the glassy phenomena found in real systems such as the pyrochlore Y_2Mo_2O_7 recently reported by Booth et al. [Booth] to contain a substantial degree of bond disorder.

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Magnetic and Thermodynamic Properties of the Collective Paramagnet-Spin Liquid Pyrochlore Tb2Ti2O7

In a recent letter [Phys. Rev. Lett. {\bf 82}, 1012 (1999)] it was found that the Tb$^{3+}$ magnetic moments in the Tb$_2$Ti$_2$O$_7$ pyrochlore lattice of corner-sharing tetrahedra remain in a {\it collective paramagnetic} state down to 70mK. In this paper we present results from d.c. magnetic susceptibility, specific heat data, inelastic neutron scattering measurements, and crystal field calculations that strongly suggest that (1) the Tb$^{3+}$ ions in Tb$_2$Ti$_2$O$_7$ possess a moment of approximatively 5$μ_{\rm B}$, and (2) the ground state $g-$tensor is extremely anisotropic below a temperature of $O(10^0)$K, with Ising-like Tb$^{3+}$ magnetic moments confined to point along a local cubic $<111>$ diagonal (e.g. towards the middle of the tetrahedron). Such a very large easy-axis Ising like anisotropy along a $<111>$ direction dramatically reduces the frustration otherwise present in a Heisenberg pyrochlore antiferromagnet. The results presented herein underpin the conceptual difficulty in understanding the microscopic mechanism(s) responsible for Tb$_2$Ti$_2$O$_7$ failing to develop long-range order at a temperature of the order of the paramagnetic Curie-Weiss temperature $θ_{\rm CW} \approx -10^1$K. We suggest that dipolar interactions and extra perturbative exchange coupling(s)beyond nearest-neighbors may be responsible for the lack of ordering of Tb$_2$Ti$_2$O$_7$.

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Transition to Long Range Magnetic Order in the Highly Frustrated Insulating Pyrochlore Antiferromagnet Gd_2Ti_2O_7

Experimental evidence from measurements of the a.c. and d.c. susceptibility, and heat capacity data show that the pyrochlore structure oxide, Gd_2Ti_2O_7, exhibits short range order that starts developing at 30K, as well as long range magnetic order at $T\sim 1$K. The Curie-Weiss temperature, $θ_{CW}$ = -9.6K, is largely due to exchange interactions. Deviations from the Curie-Weiss law occur below $\sim$10K while magnetic heat capacity contributions are found at temperatures above 20K. A sharp maximum in the heat capacity at $T_c=0.97$K signals a transition to a long range ordered state, with the magnetic specific accounting for only $\sim$ 50% of the magnetic entropy. The heat capacity above the phase transition can be modeled by assuming that a distribution of random fields acts on the $^8S_{7/2}$ ground state for Gd$^{3+}$. There is no frequency dependence to the a.c. susceptibility in either the short range or long range ordered regimes, hence suggesting the absence of any spin-glassy behavior. Mean field theoretical calculations show that no long range ordered ground state exists for the conditions of nearest-neighbor antiferromagnetic exchange and long range dipolar couplings. At the mean-field level, long range order at various commensurate or incommensurate wave vectors is found only upon inclusion of exchange interactions beyond nearest-neighbor exchange and dipolar coupling. The properties of Gd$_2Ti_2O_7 are compared with other geometrically frustrated antiferromagnets such as the Gd_3Ga_5O_{12} gadolinium gallium garnet, RE_2Ti_2O_7 pyrochlores where RE = Tb, Ho and Tm, and Heisenberg-type pyrochlore such as Y_2Mo_2O_7, Tb_2Mo_2O_7, and spinels such as ZnFe_2O_4

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Evidence for a Genuine Ferromagnetic to Paramagnetic Reentrant Phase Transition in a Potts Spin Glass Model

uch experimental and theoretical efforts have been devoted in the past twenty years to search for a genuine thermodynamic reentrant phase transition from a ferromagnetic to either a paramagnetic or spin glass phase in disordered ferromagnets. So far, no real system or theoretical model of a short-range spin glass system has been shown to convincingly display such a reentrant transition. We present here results from Migdal-Kadanoff real-space renormalization-group calculations that provide for the first time strong evidence for ferromagnetic to paramagnetic reentrance in Potts spin glasses on hierarchical lattices. Our results imply that there is no fundamental reason ruling out thermodynamic reentrant phase transitions in all non mean-field randomly frustrated systems, and may open the possibility that true reentrance might occur in some yet to be discovered real randomly frustrated materials.

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Muon Spin Relaxation Study of Reentrant Spin Glasses: Amorphous-Fe_{1-x}Mn_x

We have performed an extensive muon spin relaxation study of the well known (Fe$_{1-x}$Mn$_{x}$)$_{75}$P$_{16}$B$_6$Al$_3$ reentrant spin glass. We find a strong increase of the dynamic as well as static muon depolarization rate at the paramagnetic to ferromagnetic transition temperature, $T_c$, and at $T_f$ ($T_f<T_c$) that corresponds to the onset of strong bulk magnetic irreversabilities. We find no critical dynamic signature of a freezing of the transverse $XY$ spin components at an intermediate temperature $T_{xy}$ ($T_f < T_{xy} < T_c$) where extra static order not contributing to the magnetization starts developping.

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Observation of Spin Freezing in CaV4O9 and CaV2O5 by uSR

We have performed muon spin relaxation and susceptibility measurements of CaV_4O_9 and CaV_2O_5, systems in which spin gap-like behavior has been found. We observe spin freezing in the two compounds below 12K and 50K, respectively. Our results indicate the possibility that a substantial fraction of the of the vanadium magnetic moment is not in a spin singlet sate at low temperatures in either material.

cond-mat.str-el↗

Ferroelectric and Dipolar Glass Phases of Non-Crystalline Systems

In a recent letter [Phys. Rev. Lett. {\bf 75}, 2360 (1996)] we briefly discussed the existence and nature of ferroelectric order in positionally disordered dipolar materials. Here we report further results and give a complete description of our work. Simulations of randomly frozen and dynamically disordered dipolar soft spheres are used to study ferroelectric ordering in non-crystalline systems. We also give a physical interpretation of the simulation results in terms of short- and long-range interactions. Cases where the dipole moment has 1, 2, and 3 components (Ising, XY and XYZ models, respectively) are considered. It is found that the Ising model displays ferroelectric phases in frozen amorphous systems, while the XY and XYZ models form dipolar glass phases at low temperatures. In the dynamically disordered model the equations of motion are decoupled such that particle translation is completely independent of the dipolar forces. These systems spontaneously develop long-range ferroelectric order at nonzero temperature despite the absence of any fined-tuned short-range spatial correlations favoring dipolar order. Furthermore, since this is a nonequilibrium model we find that the paraelectric to ferroelectric transition depends on the particle mass. For the XY and XYZ models, the critical temperatures extrapolate to zero as the mass of the particle becomes infinite, whereas, for the Ising model the critical temperature is almost independent of mass and coincides with the ferroelectric transition found for the randomly frozen system at the same density. Thus in the infinite mass limit the results of the frozen amorphous systems are recovered.

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Muon Spin Relaxation Investigation of the Spin Dynamics of Geometrically Frustrated Antiferromagnets Y2Mo2O7 and Tb2Mo2O7 Static Critical Behavior of the Spin-Freezing

The spin dynamics of geometrically frustrated pyrochlore antiferromagnets Y2Mo2O7 and Tb2Mo2O7 have been investigated using muon spin relaxation. A dramatic slowing down of the moment fluctuations occurs as one approaches the spin freezing temperatures (TF=22 K and 25 K respectively) from above. Below TF there is a disordered magnetic state similar to that found in a spin glass but with a residual muon spin relaxation rate at low temperatures. These results show that there is a large density of states for magnetic excitations in these systems near zero energy.

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Static Critical Behavior of the Spin-Freezing Transition in the Geometrically Frustrated Pyrochlore Antiferromagnet Y2Mo2O7

Some frustrated pyrochlore antiferromagnets, such as Y2Mo2O7, show a spin-freezing transition and magnetic irreversibilities below a temperature Tf similar to what is observed nonlinear magnetization measurements on Y2Mo2O7 that provide strong evidence that there is an underlying thermodynamic phase transition at Tf, which is characterized by critical exponents γ\approx 2.8 and β\approx 0.8. These values are typical of those found in random spin glasses, despite the fact that the level of random disorder in Y2Mo2O7 is immeasurably small.

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Orientational Ordering in Spatially Disordered Dipolar Systems

This letter addresses basic questions concerning ferroelectric order in positionally disordered dipolar materials. Three models distinguished by dipole vectors which have one, two or three components are studied by computer simulation. Randomly frozen and dynamically disordered media are considered. It is shown that ferroelectric order is possible in spatially random systems, but that its existence is very sensitive to the dipole vector dimensionality and the motion of the medium. A physical analysis of our results provides significant insight into the nature of ferroelectric transitions.

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