arXiv subjects

Christine Martin

Publications and source records attributed to Christine Martin.

15 recordsLinked to original sources

arXiv2016

Magnetization reversal in mixed ferrite-chromite perovskites with non magnetic cation on the A-site

In this work, we have performed Monte Carlo simulations in a classical model for RFe$_{1-x}$Cr$_x$O$_3$ with R=Y and Lu, comparing the numerical simulations with experiments and mean field calculations. In the analyzed compounds, the antisymmetric exchange or Dzyaloshinskii-Moriya (DM) interaction induced a weak ferromagnetism due to a canting of the antiferromagnetically ordered spins. This model is able to reproduce the magnetization reversal (MR) observed experimentally in a field cooling process for intermediate $x$ values and the dependence with $x$ of the critical temperatures. We also analyzed the conditions for the existence of MR in terms of the strength of DM interactions between Fe$^{3+}$ and Cr$^{3+}$ ions with the x values variations.

cond-mat.mtrl-sci↗

arXiv2012

Multiferroicity in Geometrically Frustrated α-MCr_2O_4 systems (M=Ca, Sr, Ba)

We have successfully synthesized three quasi-2D geometrically frustrated magnetic compounds (α-MCr_2O_4, M=Ca, Sr, Ba) using the spark-plasma-sintering technique. All these members of the α-MCr_2O_4 family consist of the stacking planar triangular lattices of Cr$^{3+}$ spins (${\rm S}=3/2$), separated by non-magnetic alkaline earth ions. Their corresponding magnetic susceptibility, specific heat, dielectric permittivity and ferroelectric polarization are systematically investigated. A long-range magnetic ordering arises below the Néel temperature (around 40K) in each member of the α-MCr_2O_4 family, which changes to the quasi-120\degree proper-screw-type helical spin structure at low temperature. A very small but confirmed spontaneous electric polarization emerges concomitantly with this magnetic ordering. The direction of electric polarization is found within the basal triangular plane. The multiferroicity in α-MCr_2O_4 can not be explained within the frameworks of the magnetic exchange striction or the inverse Dzyaloshinskii-Moriya interaction. The observed results are more compatible with the newly proposed Arima mechanism that is associated the d-p hybridization between the ligand and transition metal ions, modified by the spin-orbit coupling. The evolution of multiferroic properties with the increasing inter-planar spacing (as M changes from Ca to Ba) reveals the importance of interlayer interaction in this new family of frustrated magnetic systems.

cond-mat.mtrl-sci↗

arXiv2011

Magneto-elastic coupling and unconventional magnetic ordering in triangular multiferroic AgCrS2

The temperature evolution of the crystal and magnetic structures of ferroelectric sulfide AgCrS2 have been investigated by means of neutron scattering. AgCrS2 undergoes at TN = 41.6 K a first-order phase transition, from a paramagnetic rhombohedral R3m to an antiferromagnetic monoclinic structure with a polar Cm space group. In addition to being ferroelectric below TN, the low temperature phase of AgCrS2 exhibits an unconventional collinear magnetic structure that can be described as double ferromagnetic stripes coupled antiferromagnetically, with the magnetic moment of Cr+3 oriented along b within the anisotropic triangular plane. The magnetic couplings stabilizing this structure are discussed using inelastic neutron scattering results. Ferroelectricity below TN in AgCrS2 can possibly be explained in terms of atomic displacements at the magneto-elastic induced structural distortion. These results contrast with the behavior of the parent frustrated antiferromagnet and spin-driven ferroelectric AgCrO2.

cond-mat.mtrl-sci↗

arXiv2009

Magnetoelectric coupling in polycrystalline FeVO4

We report coupling between magnetic and electric orders for antiferromagnetic polycrystalline FeVO4 in which magnetism-induced polarization has been recently found in noncollinear antiferromagnetic state below the second antiferromagnetic phase transition at TN2=15.7K. In this low symmetry phase space group P-1, the magnetic field dependence of electric polarization evidences a clear magnetoelectric coupling in the noncollinear spin-configured antiferromagnetic phase. The discontinuity of magnetodielectric effect observed at the vicinity of the polar to nonpolar transition evidences competition between different magnetodielectric couplings in the two different antiferromagnetic states. The existence of thermal expansion anomaly near TN2 and magnetostriction effect support magnetoelastically mediated scenario of the observed magnetoelectric effect.

cond-mat.mtrl-sci↗

arXiv2009

On the strong impact of doping in the triangular antiferromagnet CuCrO2

Electronic band structure calculations using the augmented spherical wave method have been performed for CuCrO2. For this antiferromagnetic (T_N = 24 K) semiconductor crystallizing in the delafossite structure, it is found that the valence band maximum is mainly due to the t_2g orbitals of Cr^3+ and that spin polarization is predicted with 3 mu_B per Cr^3+. The structural characterizations of CuCr1-xMgxO2 reveal a very limited range of Mg^2+ substitution for Cr^3+ in this series. As soon as x = 0.02, a maximum of 1% Cr ions substituted by Mg site is measured in the sample. This result is also consistent with the detection of Mg spinel impurities from X-ray diffraction for x = 0.01. This explains the saturation of the Mg^2+ effect upon the electrical resistivity and thermoelectric power observed for x > 0.01. Such a very weak solubility limit could also be responsible for the discrepancies found in the literature. Furthermore, the measurements made under magnetic field (magnetic susceptibility, electrical resistivity and Seebeck coefficient) support that the Cr^4+ "holes", created by the Mg^2+ substitution, in the matrix of high spin Cr^3+ (S = 3/2) are responsible for the transport properties of these compounds.

cond-mat.str-el↗

arXiv2009

Electronic structure and thermoelectric properties of CuRh(1-x)MgxO2

Electronic structure calculations using the augmented spherical wave method have been performed for CuRhO2. For this semiconductor crystallizing in the delafossite structure, it is found that the valence band maximum is mainly due to the 4d t2g orbitals of Rh^{3+}. The structural characterizations of CuRh(1-x)MgxO2 show a broad range of Mg^{2+} substitution for Rh^{3+} in this series, up to about 12%. Measurements of the resistivity and thermopower of the doped systems show a Fermi liquid-like behavior for temperatures up to about 1000K, resulting in a large weakly temperature dependent power factor. The thermopower is discussed both within the Boltzmann equation approach as based on the electronic structure calculations and the temperature independent correlation functions ratio approximation as based on the Kubo formalism.

cond-mat.str-el↗

arXiv2009

Zig-zag ladders with staggered magnetic chirality in S = 3/2 compound beta-CaCr2O4

The crystal and magnetic structures of the S = 3/2 chain antiferromagnet beta-CaCr2O4 have been investigated by means of specific heat, magnetization, muon relaxation and neutron powder diffraction between 300K and 1.5K. Owing to the original topology of the Cr3+ magnetic lattice, which can be described as a network of triangular ladders, equivalent to chains with nearest and next-nearest neighbors interactions, evolution of the magnetic scattering intensity in this compound evidences two magnetic regimes : for 21K < T < 270K, a low-dimensionality magnetic ordering of the Cr3+ spins is observed, simultaneously with a strong contraction of the ladder legs, parallel to c. Below TN = 21K, a complex antiferromagnetic ordering is evidenced, with an incommensurate propagation vector k = (0, 0, q) (q ~ 0.477 at 1.5K), as exchange interactions between ladders become significant. This complex magnetic ordering can be described as a honeycomb-like arrangement of cycloids, running along c, with staggered chiralities. The experimental observation of this staggered chirality can be understood by taking into account antisymmetric Dzyaloshinskii-Moriya exchange terms.

cond-mat.mtrl-sci↗

arXiv2008

Effect of magnetic field and temperature on the ferroelectric loop in MnWO4

The ferroelectric properties of MnWO4 single crystal have been investigated. Despite a relatively low remanent polarization, we show that the sample is ferroelectric. The shape of the ferroelectric loop of MnWO4 strongly depends on magnetic field and temperature. While its dependence does not directly correlate with the magnetocapacitance effect before the paraelectric transition, the effect of magnetic field on the ferroelectric polarization loop supports magnetoelectric coupling.

cond-mat.mtrl-sci↗

arXiv2008

Magnetic field induced ferroelectric loop in Bi0.75Sr0.25FeO3

Magnetic field induced ferroelectric hysteresis loop observed in Bi0.75Sr0.25FeO3-delta is of prime importance. The coexistence of antiferromagnetism and weak ferromagnetism is responsible for the original magnetoelastic and magnetoferroelectric properties. Upon external magnetic field application, the existence of a magnetostrictive effect supports a structural transition towards a homogeneous antiferromagnetic and ferroelectric phase. The magnetic field induced polarization is among the highest reported for BiFeO3 based systems in either thin film or bulk forms (Pr=96 microC/cm2 at 10T) while the ferroelectric coercive field is among the lowest reported (Hc=661(V/cm) at 10T). These properties make this material very attractive for technical applications.

cond-mat.mtrl-sci↗

arXiv2006

Coupled Negative magnetocapacitance and magnetic susceptibility in a Kagome staircase-like compound Co3V2O8

The dielectric constant of the Kagome staircase-like Co3V2O8 polycrystalline compound has been measured as function of temperature and magnetic field up to 14T. It is found that the application of an external magnetic field suppresses the anomaly for the dielectric constant beyond 6.1K. Furthermore, its magnetic field dependence reveals a negative magnetocapacitance which is proportional to the magnetic susceptibility, suggesting a common magnetostrictive origin for the magnetic field dependence of the two quantities. This result is very different from that obtained from the isostructural compound Ni3V2O8 that presents a peak in the dielectric constant at the incommensurate magnetic phase transition coupled to a sign change of the magnetocapacitance.

cond-mat.mtrl-sci↗

arXiv2006

Magnetic field dependence of the magnetic phase separation in Pr1-xCaxMnO3 manganites studied by small-angle neutron scattering

Transport properties of manganese oxides suggest that their colossal magnetoresistance (CMR) is due to percolation between ferromagnetic metallic (FM) clusters in an antiferromagnetic insulating (AFI) matrix. We have studied small-angle neutron scattering under applied magnetic field in CMR Pr1-xCaxMnO3 crystals for x around 0.33. Quantitative analysis of the small-angle magnetic neutron scattering shows that the magnetic heterogeneities take place at different scales. At the mesoscopic scale (200nm), the inhomogeneities correspond to the percolation of the conducting ferromagnetic phase into the insulating phases. It is at the origin of the colossal magnetoresistance of the compound. The other inhomogeneities are nanoscopic: inside the antiferromagnetic phase (AFI), there exist small ferromagnetic clusters. Inside the ferromagnetic phase which exists in absence of magnetic field in some compounds and is in fact insulating (FI), there also exist small non ferromagnetic objects. No evolution of this nanostructure is observed when the magnetic field is applied. The existence of such nanoscale objects is discussed in relation to the cationic disorder of these compounds.

cond-mat.str-el↗

arXiv2005

Non-linear effects and Joule heating in I-V curves in manganites

We study the influence of the Joule effect on the non-linear behavior of the transport I-V curves in polycrystalline samples of the manganite Pr0.8Ca0.2MnO3 by using the crystalline unit cell parameters as an internal thermometer in X-ray and neutron diffraction. We develop a simple analytical model to estimate the temperature profile in the samples. Under the actual experimental conditions we show that the internal temperature gradient or the difference between the temperature of the sample and that of the thermal bath are at the origin of the non-linearity observed in the I-V curves. Consequences on other compounds with colossal magnetoresistance are also discussed.

cond-mat.str-el↗

arXiv2003

Field dependence of the electronic phase separation in Pr0.67Ca0.33MnO3 by small angle magnetic neutron scattering

We have studied by small angle neutron scattering the evolution induced by the application of magnetic field of the coexistence of ferromagnetism (F) and antiferromagnetism (AF) in a crystal of Pr$_{0.67}$Ca$_{0.33}$MnO$_3$. The results are compared to magnetic measurements which provide the evolution of the ferromagnetic fraction. These results show that the growth of the ferromagnetic phase corresponds to an increase of the thickness of the ferromagnetic ''cabbage'' sheets.

cond-mat↗

arXiv2001

Induced Ferromagnetism and Colossal Magnetoresistance by Ir-Doping in Pr1-xCaxMnO3

The doping of the manganese site by iridium (up to 15%) in the small A cation manganites Pr_{1-x}Ca_xMnO_3 (0.4 < x < 0.8), has been investigated as a new method to suppress charge-ordering and induce CMR effects. Ir doping leads to ferromagnetism and to insulator to metal transitions, with high transition temperatures reaching 180K and CMR ratio in 7T as large as 10^4. The efficiency with which iridium induces ferromagnetism and CMR is compared to previous results obtained with other substitutions (Ru, Rh, Ni, Cr, ...). The ionic radius of the foreign cations and their mixed-valencies are found to be the main parameters governing the ability to collapse the charge-ordered state.

cond-mat.str-el↗

arXiv2001

Large Thermopower in Metallic Oxides: Misfit Cobaltites and Mangano-Ruthenates

Two different kinds of metal transition oxides have been studied for their large thermopower values. The first one corresponds to the Tl-based misfit cobaltite which is a hole-doped metal. We demonstrate that the partial Bi-substitution for Tl in this phase induces an increase of the room temperature (RT) thermopower (TEP) value. Same result is obtained with the new Pb_{1/3}SrCoO_{3+delta} misfit corresponding to the Tl complete replacement by lead. Simultaneously, the T dependence of their resistivity exhibits a re-entrance below 70-90K where a large negative magnetoresistance is observed. Magnetic measurements reveal a strong interplay between spins and charges for this class of materials. Electron-doped (n-type) perovskite manganites are a second class of potential candidates for applications. In particular, the Ru^{4+/5+} substitution for Mn in the CaMnO_3 semi-conductor induces a drastic drop of the resistivity values. Metals with large RT TEP values and not too large thermal conductivities are generated. A comparison with best known materials, Bi_2Te_3 and NaCo_2O_4 is made.

cond-mat.str-el↗