arXiv subjects

P. Manuel

Publications and source records attributed to P. Manuel.

At least 91 records · Page 5Linked to original sources

arXiv2015

$μ$SR and Neutron Diffraction Investigations on Reentrant Ferromagnetic Superconductor Eu(Fe{0.86}Ir{0.14})2As2

Results of muon spin relaxation ($μ$SR) and neutron powder diffraction measurements on a reentrant superconductor Eu(Fe$_{0.86}$Ir$_{0.14}$)$_2$As$_2$ are presented. Eu(Fe$_{0.86}$Ir$_{0.14}$)$_2$As$_2$ exhibits superconductivity at $T_{\rm c\,on} \approx 22.5$~K competing with long range ordered Eu$^{+2}$ moments below $\approx 18$ K. A reentrant behavior (manifested by nonzero resistivity in the temperature range 10--17.5 K) results from an exquisite competition between the superconductivity and magnetic order. The zero field $μ$SR data confirm the long range magnetic ordering below $T_{\rm Eu} = 18.7(2)$ K. The transition temperature is found to increase with increasing magnetic field in longitudinal field $μ$SR which along with the neutron diffraction results, suggests the transition to be ferromagnetic. The neutron diffraction data reveal a clear presence of magnetic Bragg peaks below $T_{\rm Eu}$ which could be indexed with propagation vector k = (0, 0, 0), confirming a long range magnetic ordering in agreement with $μ$SR data. Our analysis of the magnetic structure reveals an ordered magnetic moment of $6.29(5)\,μ_{\rm B}$ (at 1.8 K) on the Eu atoms and they form a ferromagnetic structure with moments aligned along the $c$-axis. No change in the magnetic structure is observed in the reentrant or superconducting phases and the magnetic structure remains same for 1.8 K $\leq T \leq T_{\rm Eu}$. No clear evidence of structural transition or Fe moment ordering was found.

cond-mat.supr-con↗

arXiv2015

Anisotropy tuned magnetic order in pyrochlore iridates

The magnetic behavior of polycrystalline samples of Er$_2$Ir$_2$O$_7$ and Tb$_2$Ir$_2$O$_7$ pyrochlores is studied by magnetization measurements and neutron diffraction. Both compounds undergo a magnetic transition at 140 and 130 K respectively, associated with an ordering of the Ir sublattice, signaled by thermomagnetic hysteresis. In Tb$_2$Ir$_2$O$_7$, we show that the Ir molecular field leads the Tb magnetic moments to order below 40 K in the all-in/all-out magnetic arrangement. No sign of magnetic long range order on the Er sublattice is evidenced in Er$_2$Ir$_2$O$_7$ down to 0.6 K where a spin freezing is detected. These contrasting behaviors result from the competition between the Ir molecular field and the different single-ion anisotropy of the rare-earths on which it is acting. Additionally, this strongly supports the all-in/all-out iridium magnetic order.

cond-mat.str-el↗

arXiv2014

Field tunable spin density wave phases in Sr3Ru2O7

The conduction electrons in a metal experience competing interactions with each other and the atomic nuclei. This competition can lead to many types of magnetic order in metals. For example, in chromium the electrons order to form a spin-density-wave (SDW) antiferromagnetic state. A magnetic field may be used to perturb or tune materials with delicately balanced electronic interactions. Here we show that the application of a magnetic field can induce SDW magnetic order in a metal, where none exists in the absence of the field. We use magnetic neutron scattering to show that the application of a large (~8T) magnetic field to the metamagnetic perovskite metal Sr3Ru2O7 can be used to tune the material through two magnetically-ordered SDW states. The ordered states exist over relatively small ranges in field (<0.4T) suggesting that their origin is due to a new mechanism related to the electronic fine structure near the Fermi energy, possibly combined with the stabilising effect of magnetic fluctuations. The magnetic field direction is shown to control the SDW domain populations which naturally explains the strong resistivity anisotropy or electronic nematic behaviour observed in this material.

cond-mat.str-el↗

arXiv2014

Symmetry of re-entrant tetragonal phase in Ba1-xNaxFe2As2: Magnetic versus orbital ordering mechanism

Magneto-structural phase transitions in Ba1-xAxFe2As2 (A = K, Na) materials are discussed for both magnetically and orbitally driven mechanisms, using a symmetry analysis formulated within the Landau theory of phase transitions. Both mechanisms predict identical orthorhombic space-group symmetries for the nematic and magnetic phases observed over much of the phase diagram, but they predict different tetragonal space-group symmetries for the newly discovered re-entrant tetragonal phase in Ba1-xNaxFe2As2 (x ~ 0.24-0.28). In a magnetic scenario, magnetic order with moments along the c-axis, as found experimentally, does not allow any type of orbital order, but in an orbital scenario, we have determined two possible orbital patterns, specified by P4/mnc1' and I4221' space groups, which do not require atomic displacements relative to the parent I4/mmm1' symmetry and, in consequence, are indistinguishable in conventional diffraction experiments. We demonstrate that the three possible space groups are however, distinct in resonant X-ray Bragg diffraction patterns created by Templeton & Templeton scattering. This provides an experimental method of distinguishing between magnetic and orbital models.

cond-mat.str-el↗

arXiv2014

Unconventional magnetic order on the hyperhoneycomb Kitaev lattice in $β$-Li2IrO3: full solution via magnetic resonant x-ray diffraction

The recently-synthesized iridate $β$-Li$_2$IrO$_3$ has been proposed as a candidate to display novel magnetic behavior stabilized by frustration effects from bond-dependent, anisotropic interactions (Kitaev model) on a three-dimensional "hyperhoneycomb" lattice. Here we report a combined study using neutron powder diffraction and magnetic resonant x-ray diffraction to solve the complete magnetic structure. We find a complex, incommensurate magnetic order with non-coplanar and counter-rotating Ir moments, which surprisingly shares many of its features with the related structural polytype "stripyhoneycomb" $γ$-Li$_2$IrO$_3$, where dominant Kitaev interactions have been invoked to explain the stability of the observed magnetic structure. The similarities of behavior between those two structural polytypes, which have different global lattice topologies but the same local connectivity, is strongly suggestive that the same magnetic interactions and the same underlying mechanism governs the stability of the magnetic order in both materials, indicating that both $β$- and $γ$-Li$_2$IrO$_3$ are strong candidates to realize dominant Kitaev interactions in a solid state material.

cond-mat.str-el↗

arXiv2014

Coupling of magnetic order to planar Bi electrons in the anisotropic Dirac metals AMnBi2 (A = Sr, Ca)

We report powder and single crystal neutron diffraction measurements of the magnetic order in AMnBi2 (A = Sr and Ca), two layered manganese pnictides with anisotropic Dirac fermions on a Bi square net. Both materials are found to order at TN approx 300 K in k = 0 antiferromagnetic structures, with ordered Mn moments at T = 10 K of approximately 3.8 muB aligned along the c axis. The magnetic structures are Neel-type within the Mn--Bi layers but the inter-layer ordering is different, being antiferromagnetic in SrMnBi2 and ferromagnetic in CaMnBi2. This allows a mean-field coupling of the magnetic order to Bi electrons in CaMnBi2 but not in SrMnBi2. We find clear evidence that magnetic order influences electrical transport. First principles calculations explain the experimental observations and suggest that the mechanism for different inter-layer ordering in the two compounds is the competition between the anteiferromagnetic superexchange and ferromagnetic double exchange carried by itinerant Bi electrons.

cond-mat.str-el↗

arXiv2014

Luttinger-Liquid Behavior in the Alternating Spin-Chain System Copper Nitrate

We determine the phase diagram of copper nitrate Cu(NO$_3$)$_2\cdot$2.5D$_2$O in the context of quantum phase transitions and novel states of matter. We establish this compound as an ideal candidate to study quasi-1D Luttinger liquids, 3D Bose-Einstein-Condensation of triplons, and the crossover between 1D and 3D physics. Magnetocaloric effect, magnetization, and neutron scattering data provide clear evidence for transitions into a Luttinger liquid regime and a 3D long-range ordered phase as function of field and temperature. Theoretical simulations of this model material allow us to fully establish the phase diagram and to discuss it in the context of dimerized spin systems.

cond-mat.str-el↗

arXiv2014

Polar and antipolar polymorphs of metastable perovskite BiFe0.5Sc0.5O3

A metastable perovskite BiFe0.5Sc0.5O3 synthesized under high-pressure (6 GPa) and high- temperature (1500 K) conditions was obtained in two different polymorphs, antipolar Pnma and polar Ima2, through an irreversible behaviour under a heating/cooling thermal cycling. The Ima2 phase represents an original type of a canted ferroelectric structure where Bi3+ cations exhibit both polar and antipolar displacements along the orthogonal [110]p and [1-10]p pseudocubic directions, respectively, and are combined with antiphase octahedral tilting about the polar axis. Both the Pnma and Ima2 structural modifications exhibit a long-range antiferromagnetic ordering with a weak-ferromagnetic component below TN ~ 220 K. Analysis of the coupling between the dipole, magnetic and elastic order parameters based on a general phenomenological approach revealed that the weak-ferromagnetism in both phases is mainly caused by the presence of the antiphase octahe- dral tilting whose axial nature directly represents the relevant part of Dzyaloshinskii vector. The magnetoelectric contribution to the spontaneous magnetization allowed in the polar Ima2 phase is described by a fifth-degree free-energy invariant and is expected to be small.

cond-mat.str-el↗

arXiv2013

Magnetic ordering with reduced cerium moments in hole-doped CeOs2Al10

The lightly hole-doped system CeOs1.94Re0.06Al10 has been studied by muon spin relaxation and neutron diffraction measurements. A long-range antiferromagnetic ordering of the Ce-sublattice with substantially reduced value of the magnetic moment 0.18(1) μ_B has been found below T_N = 21 K. Similar to the undoped parent compound, the magnetic ground state of CeOs1.94Re0.06Al10 preserves the anomalous direction of the ordered moments along the c-axis. The obtained result reveals the crucial difference between electron- and hole-doping effects on the magnetic ordering in CeOs2Al10. The former suppresses the anisotropic c-f hybridization and promotes localized Ce moments. On the contrary, the latter increases the hybridization and shifts the system towards delocalized non-magnetic state.

cond-mat.str-el↗

arXiv2013

Change of magnetic ground state by light electron-doping in CeOs2Al10

The effect of Ir substitution for Os in CeOs2Al10, with an unusually high Neel temperature of T~28.5K, has been studied by high-resolution neutron diffraction and magnetization measurements. A small amount of Ir (~ 8%) results in a pronounced change of the magnetic structure of the Ce-sublattice. The new magnetic ground state is controlled by the single ion anisotropy and implies antiferromagnetic arrangement of the Ce-moments along the a-axis, as expected from the anisotropy of the paramagnetic susceptibility. The value of the ordered moments, 0.92(1) mu_B, is substantially bigger than in the undoped compound, whereas the transition temperature is reduced down to 21K. A comparison of the observed phenomena with the recently studied CeRu1.9Rh0.1Al10 system, exhibiting similar behaviour [A. Kondo et al., J. Phys. Soc. Jpn. 82, 054709 (2013)], strongly suggests the electron doping as the main origin of the ground state changes. This provides a new way of exploring the anomalous magnetic properties of the Ce(Ru/Os)2Al10 compounds.

cond-mat.str-el↗

arXiv2013

MnSb2O6: A polar magnet with a chiral crystal structure

Structural and magnetic chiralities are found to coexist in a small group of materials in which they produce intriguing phenomenologies such as the recently discovered skyrmion phases. Here, we describe a previously unknown manifestation of this interplay in MnSb2O6, a trigonal oxide with a chiral crystal structure. Unlike all other known cases, the MnSb2O6 magnetic structure is based on co-rotating cycloids rather than helices. The coupling to the structural chirality is provided by a magnetic axial vector, related to the so-called vector chirality. We show that this unique arrangement is the magnetic ground state of the symmetric-exchange Hamiltonian, based on ab-initio theoretical calculations of the Heisenberg exchange interactions, and is stabilised by out-of-plane anisotropy. MnSb2O6 is predicted to be multiferroic with a unique ferroelectric switching mechanism.

cond-mat.str-el↗

arXiv2013

Highly frustrated magnetism in SrHo2O4: Coexistence of two types of short-range order

SrHo2O4 is a geometrically frustrated magnet in which the magnetic Ho3+ ions form honeycomb layers connected through a network of zigzag chains. At low-temperature two distinct types of short-range magnetic order can be inferred from single crystal diffraction data, collected using both polarized and unpolarized neutrons. In the (hk0) plane the diffuse scattering is most noticeable around the k = 0 positions and its intensity rapidly increases at temperatures below 0.7 K. In addition, planes of diffuse scattering at Q = (hk +/- l/2) are visible at temperatures as high as 4.5 K. These planes coexist with the broad peaks of diffuse scattering in the (hk0) plane at low-temperatures. Correlation lengths associated with the broad peaks are L ~ 150 Å in the a-b plane and L ~ 190 Å along c axis, while the correlation length associated with the diffuse scattering planes is L ~ 230 Å along the c axis at the lowest temperature. Both types of diffuse scattering are elastic in nature. The highly unusual coexistance of the two types of diffuse scattering in SrHo2O4 is likely to be the result of the presence of two crystallographically inequivalent sites for Ho3+ in the unit cell.

cond-mat.str-el↗

arXiv2013

Field-induced long-range magnetic order in the spin-singlet ground state system YbAl3C3: Neutron diffraction study

The $4f$-electron system YbAl$_3$C$_3$ with a non-magnetic spin-dimer ground state has been studied by neutron diffraction in an applied magnetic field. A long-range magnetic order involving both ferromagnetic and antiferromagnetic components has been revealed above the critical field H$_C\sim $ 6T at temperature T=0.05K. The magnetic structure indicates that the geometrical frustration of the prototype hexagonal lattice is not fully relieved in the low-temperature orthorhombic phase. The suppression of magnetic ordering by the remanent frustration is the key factor stabilizing the non-magnetic singlet ground state in zero field. Temperature dependent measurements in the applied field H=12T revealed that the long-range ordering persists up to temperatures significantly higher than the spin gap indicating that this phase is not directly related to the singlet-triplet excitation. Combining our neutron diffraction results with the previously published phase diagram, we support the existence of an intermediate disordered phase as the first excitation from the non-magnetic singlet ground state. Based on our results, we propose YbAl$_3$C$_3$ as a new material for studying the quantum phase transitions of heavy-fermion metals under the influence of geometrical frustration.

cond-mat.str-el↗

arXiv2012

A possible chiral spin-liquid phase in non-centrosymmetric $R$BaCo$_4$O$_7$

Based on a symmetry approach, we propose a possible explanation of the weak ferromagnetic component recently observed in YBaCo$_3$FeO$_7$ (Valldor et al. Phys Rev B, $\bf {84}$ 224426 (2011)) and other isostructural compounds in the high-temperature spin-liquid phase. Due to the polar nature of their crystal structure, a coupling between time-odd scalar spin chirality which we suggest as the primary order parameter and macroscopic magnetization is possible as follows from the general form of the appropriate free-energy invariant. The deduced pseudoproper coupling between both physical quantities provides a unique possibility to study the critical behaviour of the chiral order parameter.

cond-mat.str-el↗

arXiv2011

Giant improper ferroelectricity in the ferroaxial magnet CaMn7O12

In rhombohedral CaMn7O12, an improper ferroelectric polarization of magnitude 2870 μC m-2 is induced by an incommensurate helical magnetic structure that evolves below TN1 = 90 K. The electric polarization was found to be constrained to the high symmetry three-fold rotation axis of the crystal structure, perpendicular to the in-plane rotation of the magnetic moments. The multiferroicity is explained by the ferroaxial coupling mechanism, which in CaMn7O12 gives rise to the largest magnetically induced, electric polarization measured to date.

cond-mat.str-el↗

arXiv2011

The magnetic structures of the anisotropic inter-metallic compounds Er$_2$CoGa$_8$ and Tm$_2$CoGa$_8$

Two members of the iso-structural R$_2$CoGa$_8$ inter-metallic series, Er$_2$CoGa$_8$ and Tm$_2$CoGa$_8$, have been studied by powder neutron diffraction. Antiferromagnetic ordering of the rare-earth sublattices was confirmed to occur at 3.0 K and 2.0 K, respectively. Furthermore, determination of the critical exponent showed Er$_2$CoGa$_8$ to adopt a 3D universality class. In spite of a common magnetic easy axis and similar structural characteristics, the antiferromagnetic structures were found to be different for the erbium and thulium based compounds. The corresponding magnetic space groups were determined to be $P_{2a}mmm'$ and $P_Cmmm$. The difference in magnetic structures is discussed based on crystal electric field effects that are known to be prevalent in such materials.

cond-mat.str-el↗

arXiv2011

Coexistence of the long-range and short-range magnetic order components in SrEr$_2$O$_4$

Single crystal neutron diffraction reveals two distinct components to the magnetic ordering in geometrically frustrated SrEr$_2$O$_4$. One component is a long-range ordered ${\bf k}=0$ structure which appears below $T_N = 0.75$ K. Another component is a short-range incommensurate structure which manifests itself by the presence of a strong diffuse scattering signal. On cooling from higher temperatures down to 0.06 K, the partially ordered component does not undergo a pronounced phase transition. The magnetic moments in the long-range commensurate and short-range incommensurate structures are predominantly pointing along the [001] and [100] axes respectively. The unusual coexistence of two magnetic structures is probed using both unpolarised and XYZ-polarised neutron scattering techniques. The observed diffuse scattering pattern can be satisfactorily reproduced with a classical Monte Carlo simulation by using a simple model based on a ladder of triangles.

cond-mat.str-el↗

arXiv2011

Molecular spin-orbit excitations in the J_eff = 1/2 frustrated spinel GeCo$_2$O$_4$

We describe powder and single-crystal inelastic neutron scattering experiments on a spinel-type antiferromagnet GeCo$_2$O$_4$, represented by an effective total angular momentum J_eff = 1/2. Several types of non-dispersive short-range magnetic excitations were discovered. The scattering intensity maps in $\vec{Q}$ space are well reproduced by dynamical structure factor analyses using molecular model Hamiltonians. The results of analyses strongly suggest that the molecular excitations below T_N arise from a hidden molecular-singlet ground state, in which ferromagnetic subunits are antiferromagnetically coupled. The quasielastic excitations above T_N are interpreted as its precursor. A combination of frustration and J_eff = 1/2 might induce these quantum phenomena.

cond-mat.str-el↗