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P. Bonville

Publications and source records attributed to P. Bonville.

At least 55 records · Page 3Linked to original sources

Magnetic excitations in dipolar pyrochlore antiferromagnet Gd$_2$Sn$_2$O$_7$

The spin dynamics in the geometrically frustrated pyrochlore antiferromagnet $\rm Gd_2Sn_2O_7$ is studied by means of the electron spin resonance. In the ordered phase ($T_N = 1$ K), we have detected three gapped resonance modes. Their values agree well with the developed spin-wave theory which takes into account the Heisenberg nearest-neighbor exchange, the single-ion anisotropy and the long-range dipolar interactions. The theory also predicts a fourth lowest-frequency gap, which lies beyond the experimental range of frequencies, but determines the exponential decrease of the specific heat at low temperature.

cond-mat.str-el↗

Low temperature magnetization of the S=1/2 kagome antiferromagnet ZnCu_3(OH)_6Cl_2

The dc-magnetization of the unique S=1/2 kagome antiferromagnet Herbertsmithite has been measured down to 0.1K. No sign of spin freezing is observed in agreement with former muSR and ac-susceptibility results. The low temperature magnetic response is dominated by a defect contribution which exhibits a new energy scale $\simeq 1$ K, likely reflecting the coupling of the defects. The defect component is saturated at low temperature by H>8T applied magnetic fields which enables us to estimate an upper bound for the non saturated intrinsic kagome susceptibility at T=1.7K.

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Spin-liquid dynamics of pyrochlore magnets Gd2Ti2O7 and Gd2Sn2O7

The spin-liquid phase of two highly frustrated pyrochlore magnets Gd2Ti2O7 and Gd2Sn2O7 is probed using electron spin resonance in the temperature range 1.3 - 30 K. The deviation of the absorption line from the paramagnetic position ν=γH observed in both compounds below the Curie-Weiss temperature Θ_CW ~ 10 K, suggests an opening up of a gap in the excitation spectra. On cooling to 1.3 K (which is above the ordering transition T_N ~ 1.0 K) the resonance spectrum is transformed into a wide band of excitations with the gap amounting to Δ~ 26 GHz (1.2 K) in Gd2Ti2O7 and 18 GHz (0.8 K) in Gd2Sn2O7. The gaps increase linearly with the external magnetic field. For Gd2Ti2O7 this branch co-exists with an additional nearly paramagnetic line absent in Gd2Sn2O7. These low lying excitations with gaps, which are preformed in the spin-liquid state, may be interpreted as collective spin modes split by the single-ion anisotropy.

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Ferromagnetic -spin glass transition induced by pressure in Gd$_2$Mo$_2$O$_7$

R$_2$Mo$_2$O$_7$ compounds show a ferromagnetic metal-insulator spin glass transition tuned by the radius of the rare earth ion R$^{3+}$. We have studied Gd$_2$Mo$_2$O$_7$ located on the verge of the transition, by neutron diffraction on a $^{160}$Gd isotopic sample, $μ$SR and X ray diffraction using the synchrotron radiation. All measurements were done both at ambient and under applied pressure. At ambient pressure, a ferromagnetic state is observed below the Curie temperature (T$_{\rm C}$ = 70 K). The ordered magnetic moments at 1.7 K are parallel and equal to 5.7(5) $μ_{\rm B}$ and 0.8(2) $μ_{\rm B}$ for Gd and Mo, respectively. The relaxation rate measured by $μ$SR evidences strong spin fluctuations below T$_{\rm C}$ and down to the lowest temperature (6.6 K). A spin reorientation occurs in the range 20 K$<$T$<$T$_{\rm C}$. The ferromagnetic state is strongly unstable under pressure. T$_{\rm C}$ sharply decreases (down to 38 K at 1.3 GPa) and Bragg peaks start to coexist with mesoscopic ferromagnetic correlations. The ordered moments decrease under pressure. At 2.7 GPa long range magnetic order completely breaks down. In this spin glass state, Gd-Gd spin correlations remain ferromagnetic with a correlation length limited to the fourth neighbor, and Gd-Mo spin correlations turn to antiferromagnetic. The unique combination of three microscopic probes under pressure provides a detailed description of the magnetic transition, crucial for further theories.

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Ferromagnetic - spin glass transition induced by pressure in the geometrically frustrated pyrochlore (Tb$_{1-x}$La$_x$)$_2$Mo$_2$O$_7$

We have studied (Tb$_{1-x}$La$_x$)$_2$Mo$_2$O$_7$ pyrochlores by neutron diffraction and $μ$SR at ambient and under applied pressure. Substitution of Tb for La expands the lattice and induces a change from a spin-glass like state ({\itshape x}=0) to a non collinear ferromagnet ({\itshape x}=0.2). In the ferromagnetic structure, the Tb moments orient close to their local anisotropy axis as for an ordered spin ice, while the Mo moments orient close to the net moment. The $μ$SR dynamical relaxation rate shows a cusp-like peak at the Curie temperature T$_C$ and a broad anomaly at T$^\star$$<$T$_C$, suggesting a second transition of local or dynamical nature. Under pressure, the long range order breaks down and a spin glass-like state is recovered. The whole set of data provide a microscopic picture of the spin correlations and fluctuations in the region of the ferromagnetic-spin glass threshold.

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Magnetic ordering in Gd2Sn2O7: the archetypal Heisenberg pyrochlore antiferromagnet

Low-temperature powder neutron diffraction measurements are performed in the ordered magnetic state of the pyrochlore antiferromagnet Gd2Sn2O7. Symmetry analysis of the diffraction data indicates that this compound has the ground state predicted theoretically for a Heisenberg pyrochlore antiferromagnet with dipolar interactions. The difference in magnetic structures of Gd2Sn2O7 and of nominally analogous Gd2Ti2O7 is found to be determined by a specific type of third-neighbor superexchange interaction on the pyrochlore lattice between spins across empty hexagons.

cond-mat.mtrl-sci↗

Studies of R2Ti2O7 (R=Gd and Yb); new results

Specific heat and muon spin rotation and relaxation data are presented for two geometrically frustrated systems: Gd2Ti2O7 which antiferromagnetically orders and Yb2Ti2O7 which presents dynamical short range correlations at low temperature. The muon data help to characterize the spin dynamics of these two compounds.

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ESR study of the single-ion anisotropy in the pyrochlore antiferromagnet Gd2Sn2O7

Single-ion anisotropy is of importance for the magnetic ordering of the frustrated pyrochlore antiferromagnets Gd2Ti2O7 and Gd2Sn2O7. The anisotropy parameters for the Gd2Sn2O7 were measured using the electron spin resonance (ESR) technique. The anisotropy was found to be of the easy plane type, with the main constant D=140mK. This value is 35% smaller than the value of the corresponding anisotropy constant in the related compound Gd2Ti2O7.

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Magnetic density of states at low energy in geometrically frustrated systems

Using muon-spin-relaxation measurements we show that the pyrochlore compound Gd2Ti2O7, in its magnetically orderered phase below ~ 1 K, displays persistent spin dynamics down to temperatures as low as 20 mK. The characteristics of the induced muon relaxation can be accounted for by a scattering process involving two magnetic excitations, with a density of states characterized by an upturn at low energy and a small gap depending linearly on the temperature. We propose that such a density of states is a generic feature of geometrically frustrated magnetic materials.

cond-mat.str-el↗

Magnetic order and spin fluctuations in the spin liquid Tb$\_2$Sn$\_2$O$\_7$

We have studied the spin liquid Tb$\_2$Sn$\_2$O$\_7$ by neutron diffraction and specific heat measurements. Below about 2 K, the magnetic correlations change from antiferromagnetic to ferromagnetic. Magnetic order settles in two steps, with a smeared transition at 1.3(1) K then an abrupt transition at 0.87(2) K. A new magnetic structure is observed, not predicted by current models, with both ferromagnetic and antiferromagnetic character. It suggests that the spin liquid degeneracy is lifted by dipolar interactions combined with a finite anisotropy along $<111>$ axes. In the ground state, the Tb$^{3+}$ ordered moment is reduced with respect to the free ion moment (9 $μ\_{\rm B}$). The moment value of 3.3(3) $μ\_{\rm B}$ deduced from the specific heat is much smaller than derived from neutron diffraction of 5.9(1) $μ\_{\rm B}$. This difference is interpreted by the persistence of slow collective magnetic fluctuations down to the lowest temperatures.

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Low temperature spin fluctuations in geometrically frustrated Yb3Ga5O12

In the garnet structure compound Yb3Ga5O12, the Yb3+ ions (ground state effective spin S' = 1/2) are situated on two interpenetrating corner sharing triangular sublattices such that frustrated magnetic interactions are possible. Previous specific heat measurements evidenced the development of short range magnetic correlations below 0.5K and a lambda-transition at 54mK (Filippi et al. J. Phys. C: Solid State Physics 13 (1980) 1277). From 170-Yb M"ossbauer spectroscopy measurements down to 36mK, we find there is no static magnetic order at temperatures below that of the lambda-transition. Below 0.3K, the fluctuation frequency of the short range correlated Yb3+ moments progressively slows down and as the temperature tends to 0, the frequency tends to a quasi-saturated value of 3 x 10^9 s^-1. We also examined the Yb3+ paramagnetic relaxation rates up to 300K using 172-Yb perturbed angular correlation measurements: they evidence phonon driven processes.

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Magnetic properties of Yb2Mo2O7 and Gd2Mo2O7 from rare earth Mossbauer measurements

Using 170-Yb and 155-Gd Mossbauer measurements down to 0.03K, we have examined the semiconducting pyrochlore Yb2Mo2O7 where the Mo intra-sublattice interaction is anti-ferromagnetic and the metallic pyrochlore Gd2Mo2O7 where this interaction is ferromagnetic. Additional information was obtained from susceptibility, magnetisation and 172-Yb perturbed angular correlation measurements. The microscopic measurements evidence lattice disorder which is important in Yb2Mo2O7 and modest in Gd2Mo2O7. Magnetic irreversibilities occur at 17K in Yb2Mo2O7 and at 75K in Gd2Mo2O7 and below these temperatures the rare earths carry magnetic moments which are induced through couplings with the Mo sublattice. In Gd2Mo2O7, we observe the steady state Gd hyperfine populations at 0.027K are out of thermal equilibrium, indicating that Gd and Mo spin fluctuations persist at very low temperatures. Frustration is thus operative in this essentially isotropic pyrochlore where the dominant Mo intra-sublattice interaction is ferromagnetic.

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Transition and spin dynamics at very low temperature in the pyrochlores Yb2Ti2O7 and Gd2Sn2O7

The very low temperature properties of two pyrochlore compounds, Yb2Ti2O7 and Gd2Sn2O7, were investigated using an ensemble of microscopic and bulk techniques. In both compounds, a first order transition is evidenced, as well as spin dynamics persisting down to the 20mK range. The transition however has a quite different character in the two materials: whereas that in Gd2Sn2O7$ (at 1K) is a magnetic transition towards long range order, that in Yb2Ti2O7 (at 0.24K) is reminiscent of the liquid-gas transition, in the sense that it involves a 4 orders of magnitude drop of the spin fluctuation frequency; furthermore, no long range order is observed. These unusual features we attribute to frustration of the antiferromagnetic exchange interaction in the pyrochlore lattice.

cond-mat.mtrl-sci↗

The magnetic state of Yb in Kondo-lattice YbNi2B2C

We report neutron scattering experiments performed to investigate the dynamic magnetic properties of the Kondo-lattice compound YbNi2B2C. The spectrum of magnetic excitations is found to be broad, extending up to at least 150 meV, and contains inelastic peaks centred near 18 meV and 43 meV. At low energies we observe quasielastic scattering with a width Gamma = 2.1 meV. The results suggest a Yb3+ ground state with predominantly localized 4f electrons subject to (i) a crystalline electric field (CEF) potential, and (ii) a Kondo interaction, which at low temperatures is about an order of magnitude smaller than the CEF interaction. From an analysis of the dynamic magnetic response we conclude that the crystalline electric field acting on the Yb ions has a similar anisotropy to that in other RNi2B2C compounds, but is uniformly enhanced by almost a factor of 2. The static and dynamic magnetic properties of YbNi2B2C are found to be reconciled quite well by means of an approximation scheme to the Anderson impurity model, and this procedure also indicates that the effective Kondo interaction varies with temperature due to the crystal field splitting. We discuss the nature of the correlated-electron ground state of YbNi2B2C based on these and other experimental results, and suggest that this compound might be close to a quantum critical point on the non-magnetic side.

cond-mat.str-el↗

First Order Transition in the Spin Dynamics of Geometrically Frustrated Yb2Ti2O7

Using neutron diffraction, 170Yb Mossbauer and muSR spectroscopies, we have examined the pyrochlore Yb2Ti2O7 where the Yb3+ S'=1/2 ground state has planar anisotropy. Below ~0.24K, the temperature of the known specific heat lambda transition, there is no long range magnetic order. We show that the transition corresponds to a first order change in the fluctuation rate of the Yb3+ spins. Above the transition temperature, the rate, in the GHz range, follows a thermal excitation law, whereas below, the rate, in the MHz range, is essentially temperature independent indicative of a quantum fluctuation regime.

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Effective nuclear temperature in a fluctuating spin system

We report on very low temperature (27 mK) Mossbauer absorption spectra on Gd 155 in the Heisenberg frustrated antiferromagnets Gd2 Sn2 O7 (GdSn) and Gd2 Ti2 O7. We show that electronic fluctuations of correlated Gd3+ moments are present near T=0 in GdSn by observing that the hyperfine levels are out of equilibrium. Using a model spin 1/2 system, submitted to a magnetic (hyperfine) field reversing randomly in time, we find an analytical expression for the stationary probability distribution of the level populations (or magnetization). This quantity is a simple function of the ratio of the nuclear relaxation time to the average electronic flip time. These two time scales are found to be of the same magnitude in GdSn, and we discuss a relevant mechanism for nuclear relaxation and the influence of electronic fluctuations on the nuclear specific heat.

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Non-Langevin behaviour of the uncompensated magnetisation in nanoparticles of artificial ferritin

The magnetic behaviour of nanoparticles of antiferromagnetic ferritin has been investigated by 57Fe Mossbauer absorption spectroscopy and magnetisation measurements, in the temperature range 2.5K-250K and with magnetic fields up to 7T. Samples containing nanoparticles with an average number of Fe atoms ranging from 400 to 2500 were studied. The value of the anisotropy energy per unit volume was determined and found to be in the range 3-6 10**5 ergs/cm3, which is a value typical for ferric oxides. By comparing the results of the two experimental methods at large field, we show that, contratry to what is currently assumed, the uncompensated magnetisation of the feritin cores in the superparamagnetic regime does not follow a Langevin law. For magnetic fields below the spin-flop field, we propose an approximate law for the field and temperature variation of the uncompensated magnetisation which has so far never been applied in antiferromagnetic systems. This approach should more generally hold for randomly oriented antiferro- magnetic nanoparticles systems with weak uncompensated moments.

cond-mat.mtrl-sci↗

Search for incoherent tunnel fluctuations of the magnetisation in nanoparticles of artificial ferritin

The magnetic behaviour of nanoparticles of antiferromagnetic ferritin, with a mean Fe loading of 410 atoms per core, has been investigated by 57Fe Mossbauer absorption spectroscopy down to very low temperature (34mK). In previous experi- ments of frequency dependent magnetic susceptibility and magnetic noise performed at 25mK in similar samples, it was claimed that a resonance at a frequency of about 10**8 Hz, due to a macroscopic coherent state, had been observed. However, our search of incoherent tunnel fluctuations around 10**8 Hz using 57Fe Mossbauer spectroscopy, whose "window" of measurement of fluctuation frequencies lies in this frequency range, was unsuccessful. This casts a doubt about the previous observa- tion of macroscopic quantum coherence in ferritin.

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