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R. Mathieu

Publications and source records attributed to R. Mathieu.

At least 37 records · Page 2Linked to original sources
arXiv2012

Investigation of the magnetic phase transition and magnetocaloric properties of the Mn$_2$FeSbO$_6$ ilmenite

The magnetic phase transition and magnetocaloric properties of mineral and synthetic melanostibite Mn$_2$FeSbO$_6$ with ilmenite-type structure have been studied. Mn$_2$FeSbO$_6$ orders ferrimagnetically below 270 K and is found to undergo a second-order magnetic phase transition. The associated magnetic entropy change amounts to 1.7 J/kgK for the mineral and 1.8 J/kgK synthetic melanostibite for 5 T field change. For the synthetic Mn$_2$FeSbO$_6$ the adiabatic temperature change was estimated from magnetic- and specific heat measurements and amounts to 0.2 K in 1 T field change. Perspectives of the promising functional properties of Mn$_2$FeSbO$_6$-based materials are discussed.

cond-mat.mtrl-sci↗
arXiv2012

Ferrimagnetism, Antiferromagnetism and Magnetic Frustration in La$_{2-x}$Sr$_{x}$CuRuO$_{6}$ (0 <= x <= 1)

We studied structural and magnetic properties of a series of insulating double perovskite compounds, La$_{2-x}$Sr$_{x}$CuRuO$_{6}$ (0 $\le$ x $\le$ 1), representing doping via \textit{A}-site substitution. The end members La$_{2}$CuRuO$_{6}$ and LaSrCuRuO$_{6}$ form in monoclinic structure while the intermediate Sr doped compounds stabilise in triclinic structure. The Cu and Ru ions sit on alternate B-sites of the perovskite lattice with $\sim$15% anti-site defects in the undoped sample while the Sr doped samples show a tendency to higher ordering at B-sites. The undoped (x = 0) compound shows a ferrimagnetic-like behaviour at low temperatures. In surprising contrast to the usual expectation of an enhancement of ferromagnetic interaction on doping, an antiferromagnetic-like ground state is realized for all doped samples (x $>$ 0). Heat capacity measurements indicate the absence of any long range magnetic order in any of these compounds. The magnetic relaxation and memory effects observed in all compounds suggest glassy dynamical properties associated with magnetic disorder and frustration. We show that the observed magnetic properties are dominated by the competition between the nearest neighbour Ru -- O -- Cu 180$^\circ$ superexchange interaction and the next nearest neighbour Ru -- O -- O -- Ru 90$^\circ$ superexchange interaction as well as by the formation of anti-site defects with interchanged Cu and Ru positions. Our calculated exchange interaction parameters from first principles calculations for $x$ = 0 and $x$ = 1 support this interpretation.

cond-mat.str-el↗
arXiv2012

Mott versus Slater-type metal-insulator transition in Mn-substituted Sr3Ru2O7

We present a temperature-dependent x-ray absorption (XAS) and resonant elastic x-ray scattering (REXS) study of the metal-insulator transition (MIT) in Sr3(Ru1-xMnx)2O7. The XAS results reveal that the MIT drives the onset of local antiferromagnetic correlations around the Mn impurities, a precursor of the long-range antiferromagnetism detected by REXS at T_order<T_MIT. This establishes that the MIT is of the Mott-type (electronic correlations) as opposed to Slater-type (magnetic order). While this behavior is induced by Mn impurities, the (1/4,1/4,0) order exists for a wide range of Mn concentrations, and points to an inherent instability of the parent compound.

cond-mat.str-el↗
arXiv2012

Near room-temperature colossal magnetodielectricity and multiglass properties in partially-disordered La2NiMnO6

We report magnetic, dielectric and magnetodielectric responses of pure monoclinic bulk phase of partially-disordered La2NiMnO6, exhibiting a spectrum of unusual properties and establish that this system intrinsically is a true multiglass with a large magnetodielectric coupling (8-20%) over a wide range of temperatures (150 - 300 K). Specifically, our results establish a unique way to obtain colossal magnetodielectricity, independent of any striction effects, by engineering the asymmetric hopping contribution to the dielectric constant via the tuning of the relative spin orientations between neighboring magnetic ions in a transition metal oxide system. We discuss the role of anti-site (Ni-Mn) disorder in emergence of these unusual properties.

cond-mat.mtrl-sci↗
arXiv2012

Spatially controlled formation of superparamagnetic (Mn,Ga)As nanocrystals in high temperature annealed (Ga,Mn)As/GaAs superlattices

The annealing-induced formation of (Mn,Ga)As nanocrystals in (Ga,Mn)As/GaAs superlattices was studied by X-ray diffraction, transmission electron microscopy and magnetometry. The superlattice structures with 50 A thick (Ga,Mn)As layers separated by 25, 50 and 100 A thick GaAs spacers were grown by molecular beam epitaxy at low temperature (250 C), and then annealed at high temperatures of: 400, 560 and 630 C. The high temperature annealing causes decomposition to GaMnAs ternary alloy and formation of (Mn,Ga)As nanocrystals inside the GaAs matrix. The nanocrystals are confined in the planes that were formerly occupied by (Ga,Mn)As layers for up to the 560 C of annealing and diffuse throughout the GaAs spacer layers at 630 C annealing. The corresponding magnetization measurements show the evolution of the magnetic properties of as-grown and annealed samples from ferromagnetic, through superparamagnetic to the combination of both.

cond-mat.mtrl-sci↗
arXiv2011

Structural and magnetic properties of Mn3-xCdxTeO6 (x = 0, 1, 1.5 and 2)

Mn3TeO6 exhibits a corundum-related A3TeO6 structure and a complex magnetic structure involving two magnetic orbits for the Mn atoms [*]. Mn3-xCdxTeO6 (x=0, 1, 1.5 and 2) ceramics were synthesized by solid state reaction and investigated using X-ray powder diffraction, electron microscopy, calorimetric and magnetic measurements. Cd2+ replaces Mn2+ cations without greatly affecting the structure of the compound. The Mn and Cd cations were found to be randomly distributed over the A-site. Magnetization measurements indicated that the samples order antiferromagnetically at low temperature with a transition temperature that decreases with increasing Cd doping. The nuclear and magnetic structure of one specially prepared 114Cd containing sample: Mn1.5(114Cd)1.5TeO6, was studied using neutron powder diffraction over the temperature range 2 to 295 K. Mn1.5(114Cd)1.5TeO6 was found to order in an incommensurate helical magnetic structure, very similar to that of Mn3TeO6 [*]. However, with a lower transition temperature and the extension of the ordered structure confined to order 240(10) Å. [*] S. A. Ivanov et al. Mater. Res. Bull. 46 (2011) 1870.

cond-mat.mtrl-sci↗
arXiv2011

Temperature-dependent multi-k magnetic structure in multiferroic Co3TeO6

A complex magnetic order of the multiferroic compound Co3TeO6 has been revealed by neutron powder diffraction studies on ceramics and crushed single crystals. The compound adopts a monoclinic structure (s.g. C2/c) in the studied temperature range 2 K - 300 K but exhibits successive antiferromagnetic transitions at low temperature. Incommensurate antiferromagnetic order with the propagation vector k1 = (0, 0.485, 0.055) sets in at 26 K. A transition to a second antiferromagnetic structure with k2 = (0, 0, 0) takes place at 21.1 K. Moreover, a transition to a commensurate antiferromagnetic structure with k3 = (0, 0.5, 0.25) occurs at 17.4 K. The magnetic structures have been determined by neutron powder diffraction using group theory analysis as a preliminary tool. Different coordinations of the Co2+ ions involved in the low-symmetry C2/c structure of Co3TeO6 render the exchange-interaction network very complex by itself. The observed magnetic phase transformations are interpreted as an evidence of competing magnetic interactions. The temperature dependent changes in the magnetic structure, derived from refinements of high-resolution neutron data, are discussed and possible mechanisms connected with the spin reorientations are described.

cond-mat.mtrl-sci↗
arXiv2011

Tuning of dielectric properties and magnetism of SrTiO3 by site-specific doping of Mn

Combining experiments with first principles calculations, we show that site-specific doping of Mn into SrTiO3 has a decisive influence on the dielectric properties of these doped systems. We find that phonon contributions to the dielectric constant invariably decrease sharply on doping at any site. However, a sizable, random dipolar contribution only for Mn at the Sr site arises from a strong off-centric displacement of Mn in spite of Mn being in a non-d0 state; this leads to a large dielectric constant at higher temperatures and gives rise to a relaxor ferroelectric behavior at lower temperatures. We also investigate magnetic properties in detail and critically reevaluate the possibility of a true multi-glass state in such systems.

cond-mat.mtrl-sci↗
arXiv2011

Complex magnetism and magnetic field-driven electrical polarization in Co$_3$TeO$_6$

The magnetic and electrical properties of Co$_3$TeO$_6$ single-crystals with corundum related structure reveal a magnetic-field induced polarization below 21 K. A sharp peak in the specific heat at \approx 18 K indicates a reconstructive-type first-order phase transition. From second-harmonic generation (SHG) measurements breaking of inversion symmetry is evident and the point-group symmetry was determined as m. The temperature and magnetic-field dependence of the magnetic and electrical polarizations are discussed in the light of the SHG results.

cond-mat.str-el↗
arXiv2011

Short-range spin order and frustrated magnetism in Mn2InSbO6 and Mn2ScSbO6

The complex metal oxides Mn2ASbO6 (A=In, Sc) with a corundum-related structure A3BO6 have been prepared as polycrystalline powders by a solid state reaction route. The crystal structure and magnetic properties have been investigated using a combination of X-ray and neutron powder diffraction, electron microscopy, calorimetric and magnetic measurements. At room temperature these compounds adopt a trigonal structure, space group R-3 with a = 8.9313(1) Å, c = 10.7071(2) Å (for In) and a = 8.8836(1) Å, c = 10.6168(2) Å (for Sc) which persists down to 1.6 K. The Mn and A cations were found to be randomly distributed over the A-sites. The overall behavior of the magnetization of Mn2InSbO6 and Mn2ScSbO6 is quite similar. In spite of the relatively large amount of Mn ions on the A-site, only short-ranged magnetism is observed. Neutron diffraction patterns of Mn2InSbO6 showed no evidence of a long-range magnetic ordering at 1.6 K, instead only a weak diffuse magnetic peak was observed at low temperatures. The factors governing the observed structural and magnetic properties of Mn2ASbO6 are discussed and compared with those of other Mn-containing complex metal oxides with a corundum-related structure. The influence of the A-cation sublattice on magnetic properties is also considered.

cond-mat.mtrl-sci↗
arXiv2011

Magnetic order near 270 K in mineral and synthetic Mn$_2$FeSbO$_6$ ilmenite

The structural and magnetic properties of Mn$_2$FeSbO$_6$ single-crystalline mineral and ceramic samples synthesized under thermobaric treatment have been investigated, and compared to theoretical predictions based on first-principles electronic structure calculations. This ilmenite system displays a sharp magnetic transition just below the room temperature related to a ferrimagnetic ordering of the Mn$^{2+}$ and Fe$^{3+}$ cations, which makes Mn$_2$FeSbO$_6$ a promising candidate for designing functional magnetic materials.

cond-mat.str-el↗
arXiv2011

New type of incommensurate magnetic ordering in Mn3TeO6

The complex metal oxide Mn3TeO6 exhibits a corundum related structure and has been prepared both in forms of single crystals by chemical transport reactions and of polycrystalline powders by a solid state reaction route. The crystal structure and magnetic properties have been investigated using a combination of X-ray and neutron powder diffraction, electron microscopy, calorimetric and magnetic measurements. At room temperature this compound adopts a trigonal structure, space group R3 with a = 8.8679(1) Å, c = 10.6727(2) Å. A long-range magnetically ordered state is identified below 23 K. An unexpected feature of this magnetic structure is several types of Mn-chains. Under the action of the incommensurate magnetic propagation vector k = [0, 0, 0.4302(1)] the unique Mn site is split into two magnetically different orbits. One orbit forms a perfect helix with the spiral axis along the c-axis while the other orbit has a sine wave character along the c-axis.

cond-mat.mtrl-sci↗
arXiv2011

Influence of the $A$ cation on the low-temperature antiferromagnetism of ordered antiferroelectric $A_2$CoTeO$_6$ perovskites

We have investigated the structural and magnetic properties of antiferroelectric $A_2$CoTeO$_6$ perovskites with $A$ = Cd, Ca, Sr, Pb, and Ba. All compounds are antiferromagnetic at low temperatures, with the antiferromagnetic transition temperature slightly decreasing with decreasing ionic size of the $A$ cation. Such a decrease in antiferromagnetic interaction is not observed in $A^{2+}_2$Co$M^{6+}$O$_6$ materials with other $M^{6+}$ cations of similar ionic sizes, suggesting that Te$^{6+}$ cations affect the electronic and in turn the magnetic structure of the system.

cond-mat.str-el↗
arXiv2011

Voids and Mn-rich inclusions in a (Ga,Mn)As ferromagnetic semiconductor investigated by transmission electron microscopy

Voids adjacent to both cubic (ZnS-type) and hexagonal (NiAs-type) Mn-rich nanocrystals are characterized using aberration-corrected transmission electron microscopy in annealed Ga0.995Mn0.005As magnetic semiconductor specimen grown by molecular beam epitaxy. Nano-beam electron diffraction measurements suggest that the nanocrystals exhibit deviations in lattice parameter from that of bulk MnAs. In situ annealing inside the electron microscope is used to study the nucleation, coalescence, and grain growth of individual nanocrystals. After annealing at 903 K, the magnetic transition temperature of the specimen likely to be dominated by the presence of cubic ferromagnetic nanocrystals.

cond-mat.mtrl-sci↗
arXiv2010

Neutron diffraction studies and the magnetism of an ordered perovskite: Ba2CoTeO6

The complex perovskite Ba2CoTeO6 (BCTO) has been synthesised, and the crystal structure and magnetic properties have been investigated using a combination of X-ray and neutron powder diffraction, electron microscopy and dielectric, calorimetric and magnetic measurements. It was shown that at room temperature this compound adopts the 6L-trigonal perovskite structure, space group P-3m (N 164) (a= 5.7996(1)Å, c=14.2658(3)Å). The structure comprises dimers of face-sharing octahedra as well as octahedra which share only vertices with their neighbours. A long-range antiferromagnetically ordered state has been identified from neutron diffraction and magnetic studies. The magnetic diffraction peaks were registered below the magnetic transition at about 15 K and a possible model for the magnetic structure is proposed. The structural and magnetic features of this compound are discussed and compared with those of other Co-based quaternary oxides adopting the perovskite structure.

cond-mat.mtrl-sci↗
arXiv2010

Structural and magnetic properties of the ordered perovskite Pb2CoTeO6

The complex perovskite Pb2CoTeO6 (PCTO) has been prepared as polycrystalline powders by solid state reaction route, and the crystal structure and magnetic properties have been investigated using a combination of X-ray and neutron powder diffraction, electron microscopy, dielectric, calorimetric and magnetic measurements. It was shown that at room temperature this compound adopts a trigonal perovskite structure, space group R-3 (a= 5.6782(1)Å, c= 13.8552(3)Å). The compound undergoes a number of temperature-induced phase transitions and adopts four different structures in the temperature range 5-500 K: monoclinic in P21/n(5<T<125K, tilt system (a+b-b-)), monoclinic in I2/m (125<T<210 K, tilt system (a0b-b-)), rhombohedral in R-3 (210<T<370K, tilt system (a-a-a-)), and finally cubic in Fm-3m (above 370K without any tilting). These structural phase transitions are coupled to a change in the dielectric constant and the heat capacity around 210 and 370K. A long-range antiferromagnetically ordered state has been identified from neutron powder diffraction and magnetic studies at different temperatures. Magnetic diffraction peaks were registered below the transition at about 16 K and a possible model for the magnetic structure is proposed. Possible coexistence of long-range ordering of electrical dipoles and magnetic moments at low temperatures making PCTO a multiferroic candidate is discussed and compared with those of other Co-based quaternary oxides adopting the perovskite structure.

cond-mat.mtrl-sci↗
arXiv2010

Memory and rejuvenation in a spin glass

The temperature dependence of the magnetisation of a Cu(Mn) spin glass ($T_g$ $\approx$ 57 K) has been investigated using weak probing magnetic fields ($H$ = 0.5 or 0 Oe) and specific thermal protocols. The behaviour of the zero-field cooled, thermoremanent and isothermal remanent magnetisation on (re-)cooling the system from a temperature (40 K) where the system has been aged is investigated. It is observed that the measured magnetisation is formed by two parts: (i) a temperature- and observation time-dependent thermally activated relaxational part governed by the age- and temperature-dependent response function and the (latest) field change made at a lower temperature, superposed on (ii) a weakly temperature-dependent frozen-in part. Interestingly we observe that the spin configuration that is imprinted during an elongated halt in the cooling, if it is accompanied by a field induced magnetisation, also includes a unidirectional excess magnetisation that is recovered on returning to the ageing temperature.

cond-mat.dis-nn↗