arXiv subjects

Pascal Manuel

Publications and source records attributed to Pascal Manuel.

At least 37 records · Page 2Linked to original sources

arXiv2023

Evidence for Conical Magnetic Structure in M-type BaFe12O19 Hexaferrite: A Combined Single-Crystal XMCD and Neutron Diffraction Study

The magnetic ground state of BaFe12O19 (BFO) was investigated using X-ray absorption at 1.2 K and 1.5 K, respectively. The XMCD measurements on single-crystals of BFO in grazing incidence geometry reveal the canting of the spins away from the c-axis of the hexagonal unit cell. Single-crystal neutron diffraction studies reveal magnetic satellite peaks along the 00l reciprocal lattice row around the forbidden l = 2n +/- 1 positions confirming conical-type magnetic structure in the ground state of BFO. The observation of the conical magnetic structure of BFO opens the possibility of type-II multiferroicity in undoped BFO also.

cond-mat.mtrl-sci↗

arXiv2023

Successive magnetic phase transitions with magnetoelastic and magnetodielectric coupling in the ordered triple perovskite Sr$_3$CaRu$_2$O$_9$

We report a comprehensive temperature-dependent investigation of the 1:2 ordered triple perovskite system Sr$_3$CaRu$_2$O$_9$. It crystallizes in the monoclinic structure with space group $P21/c$, consisting of corner-sharing CaO$_6$ and RuO$_6$ octahedra. Using DC magnetization and neutron diffraction measurements, we show that this system undergoes successive magnetic transitions ~190 K and ~160 K. From the analysis of the temperature-dependent neutron diffraction and dielectric data, we demonstrate two distinguishing features of the Sr$_3$CaRu$_2$O$_9$ system: (i) magnetoelastic coupling associated with the two magnetic transitions, as revealed by a change in the unit cell volume, direct Ru-Ru distance, and bond angles and (ii) magnetodielectric coupling, as revealed by the anomalies across the two magnetic transitions. The present results would add significantly to the current understanding of the triple perovskites with incipient spin-orbit coupling.

cond-mat.str-el↗

arXiv2023

Charge density wave-templated spin cycloid in topological semimetal $NdSb_{x}Te_{2-x-δ}$

Magnetic topological semimetals present open questions regarding the interplay of crystal symmetry, magnetism, band topology, and electron correlations. $LnSb_{x}Te_{2-x-δ}$ (Ln= lanthanide) is a family of square-net-derived topological semimetals that allows compositional control of band filling, and access to different topological states via an evolving charge density wave (CDW) distortion. Previously studied Gd and Ce members containing a CDW have shown complex magnetic phase diagrams, which implied that spins localized on Ln interact with the CDW, but to this date, no magnetic structures have been solved within the CDW regime of this family of compounds. Here, we report on the interplay of the CDW with magnetism in $NdSb_{x}Te_{2-x-δ}$, by comparing the undistorted square net member $NdSb_{0.94}Te_{0.92}$ with the CDW-distorted phase $NdSb_{0.48}Te_{1.37}$, via single-crystal x-ray diffraction, magnetometry, heat capacity, and neutron powder diffraction. $NdSb_{0.94}Te_{0.92}$ is a collinear antiferromagnet with $T_N$ $\sim$ 2.7 K, where spins align antiparallel to each other, but parallel to the square net of the nuclear structure. $NdSb_{0.48}Te_{1.37}$ exhibits a nearly five-fold modulated CDW ($q_{CDW}=0.18b^*$), isostructural to other $LnSb_{x}Te_{2-x-δ}$ at similar x. $NdSb_{0.48}Te_{1.37}$ displays more complex magnetism with $T_N = 2.3 K$, additional metamagnetic transitions, and an elliptical cycloid magnetic structure with $q_{mag}=-0.41b^*$.The magnitudes of $q_{CDW}$ and $q_{mag}$ exhibit a integer relationship, $1+2q_{mag}=q_{CDW}$, implying a coupling between the CDW and magnetic structure. Given that the CDW is localized within the nonmagnetic distorted square net, we propose that conduction electrons "template" the spin modulation via the Ruderman-Kittel-Kasuya-Yosida interaction.

cond-mat.mtrl-sci↗

arXiv2023

Fragmented spin ice and multi-$k$ ordering in rare-earth antiperovskites

We study near-neighbour and dipolar Ising models on a lattice of corner-sharing octahedra. In an extended parameter range of both models, frustration between antiferromagnetism and a spin-ice-like three-in-three-out rule stabilises a Coulomb phase with correlated dipolar and quadrupolar spin textures, both yielding distinctive neutron-scattering signatures. Strong further-neighbour perturbations cause the two components to order independently, resulting in unusual multi-$k$ orders. We propose experimental realisations of our model in rare-earth antiperovskites.

cond-mat.str-el↗

arXiv2022

Probing the Manipulation of Antiferromagnetic Order in CuMnAs Films Using Neutron Diffraction

We describe measurements of the uniaxial magnetic anisotropy and spin-flop rotation of the Néel vector in antiferromagnetic CuMnAs thin films using neutron diffraction. The suppression of the magnetic (100) peak under magnetic fields is observed for films as thin as 20 nm indicating that they undergo a spin-flop transition. Good agreement is found between neutron diffraction and electron transport measurements of the spin-flop rotation in the same layer, with a similar shape and hysteresis of the obtained curves, while the neutron measurements provide a quantitative determination of the spin flop extent throughout the antiferromagnet layer.

cond-mat.mtrl-sci↗

arXiv2022

Creating and controlling Dirac fermions, Weyl fermions, and nodal lines in the magnetic antiperovskite Eu$_3$PbO

The band topology of magnetic semimetals is of interest both from the fundamental science point of view and with respect to potential spintronics and memory applications. Unfortunately, only a handful of suitable topological semimetals with magnetic order have been discovered so far. One such family that hosts these characteristics is the antiperovskites, A$_3$BO, a family of 3D Dirac semimetals. The A=Eu$^{2+}$ compounds magnetically order with multiple phases as a function of applied magnetic field. Here, by combining band structure calculations with neutron diffraction and magnetic measurements, we establish the antiperovskite Eu$_3$PbO as a new topological magnetic semimetal. This topological material exhibits a multitude of different topological phases with ordered Eu moments which can be easily controlled by an external magnetic field. The topological phase diagram of Eu$_3$PbO includes an antiferromagnetic Dirac phase, as well as ferro- and ferrimagnetic phases with both Weyl points and nodal lines. For each of these phases, we determine the bulk band dispersions, the surface states, and the topological invariants by means of $\textit{ab-initio}$ and tight-binding calculations. Our discovery of these topological phases introduces Eu$_3$PbO as a new platform to study and manipulate the interplay of band topology, magnetism, and transport.

cond-mat.mtrl-sci↗

arXiv2021

Heisenberg spins on an anisotropic triangular lattice: PdCrO2 under uniaxial stress

When Heisenberg spins interact antiferromagnetically on a triangular lattice and nearest-neighbor interactions dominate, the ground state is 120$^{\circ}$ antiferromagnetism. In this work, we probe the response of this state to lifting the triangular symmetry, through investigation of the triangular antiferromagnet PdCrO$_2$ under uniaxial stress by neutron diffraction and resistivity measurements. The periodicity of the magnetic order is found to change rapidly with applied stress; the rate of change indicates that the magnetic anisotropy is roughly forty times the stress-induced bond length anisotropy. At low stress, the incommensuration period becomes extremely long, on the order of 1000 lattice spacings; no locking of the magnetism to commensurate periodicity is detected. Separately, the magnetic structure is found to undergo a first-order transition at a compressive stress of $\sim$0.4 GPa, at which the interlayer ordering switches from a double- to a single-q structure.

cond-mat.str-el↗

arXiv2021

Magnetic field induced quantum spin liquid in the two coupled trillium lattices of K$_2$Ni$_2$(SO$_4$)$_3$

Quantum spin liquids are exotic states of matter which form when strongly frustrated magnetic interactions induce a highly entangled quantum paramagnet far below the energy scale of the magnetic interactions. Three-dimensional cases are especially challenging due to the significant reduction of the influence of quantum fluctuations. Here, we report the magnetic characterization of {\kni} forming a three dimensional network of Ni$^{2+}$ spins. Using density functional theory calculations we show that this network consists of two interconnected spin-1 trillium lattices. In the absence of a magnetic field, magnetization, specific heat, neutron scattering and muon spin relaxation experiments demonstrate a highly correlated and dynamic state, coexisting with a peculiar, very small static component exhibiting a strongly renormalized moment. A magnetic field $B \gtrsim 4$ T diminishes the ordered component and drives the system in a pure quantum spin liquid state. This shows that a system of interconnected $S=1$ trillium lattices exhibit a significantly elevated level of geometrical frustration.

cond-mat.str-el↗

arXiv2021

Discovery of Superconductivity in (Ba,K)SbO$_{3}$

Superconducting bismuthates (Ba,K)BiO$_{3}$ (BKBO) constitute an interesting class of superconductors in that superconductivity with a remarkably high $T_\mathrm{c}$ of 30 K arises in proximity to charge density wave (CDW) order. Prior understanding on the driving mechanism of the CDW and superconductivity emphasizes the role of either bismuth (negative $U$ model) or oxygen ions (ligand hole model). While holes in BKBO presumably reside on oxygen owing to their negative charge transfer energy, so far there has been no other comparative material studied. Here, we introduce (Ba,K)SbO$_{3}$ (BKSO) in which the Sb 5$s$ orbital energy is higher than that of the Bi 6$s$ orbitals enabling tuning of the charge transfer energy from negative to slightly positive. The parent compound BaSbO$_{3-δ}$ shows a larger CDW gap compared to the undoped bismuthate BaBiO$_{3}$. As the CDW order is suppressed via potassium substitution up to 65 %, superconductivity emerges, rising up to $T_\mathrm{c}$ = 15 K. This value is lower than the maximum $T_\mathrm{c}$ of BKBO, but higher by more than a factor of two at comparable potassium concentrations. The discovery of an enhanced CDW gap and superconductivity in BKSO indicates that the sign of the charge transfer energy may not be crucial, but instead strong metal-oxygen covalency plays the essential role in constituting a CDW and high-$T_\mathrm{c}$ superconductivity in the main-group perovskite oxides.

cond-mat.supr-con↗

arXiv2021

Magnetic and electronic ordering phenomena in the [Ru$_2$O$_6$] honeycomb lattice compound AgRuO$_3$

The silver ruthenium oxide AgRuO$_3$ consists of honeycomb [Ru$_2^{5+}$O$_6^{2-}$] layers, and can be considered an analogue of SrRu$_2$O$_6$ with a different intercalation stage. We present measurements of magnetic susceptibility and specific heat on AgRuO$_3$ single crystals which reveal a sharp antiferromagnetic transition at 342(3)K. The electrical transport in single crystals of AgRuO$_3$ is determined by a combination of activated conduction over an intrinsic semiconducting gap of $\approx$ 100 meV and carriers trapped and thermally released from defects. From powder neutron diffraction data a Néel-type antiferromagnetic structure with the Ru moments along the $c$ axis is derived. Raman and muon spin rotation spectroscopy measurements on AgRuO$_3$ powder samples indicate a further weak phase transition or a crossover in the temperature range 125-200 K. The transition does not show up in magnetic susceptibility and its origin is argued to be related to defects but cannot be fully clarified. The experimental findings are complemented by DFT-based electronic structure calculations. It is found that the magnetism in AgRuO$_3$ is similar to that of SrRu$_2$O$_6$, however with stronger intralayer and weaker interlayer magnetic exchange interactions.

cond-mat.str-el↗

arXiv2020

Magnetically induced metal-insulator transition in Pb2CaOsO6

We report on the structural, magnetic, and electronic properties of two new double-perovskites synthesized under high pressure; Pb2CaOsO6 and Pb2ZnOsO6. Upon cooling below 80 K, Pb2CaOsO6 simultaneously undergoes a metal--insulator transition and develops antiferromagnetic order. Pb2ZnOsO6, on the other hand, remains a paramagnetic metal down to 2 K. The key difference between the two compounds lies in their crystal structure. The Os atoms in Pb2ZnOsO6 are arranged on an approximately face-centred cubic lattice with strong antiferromagnetic nearest-neighbor exchange couplings. The geometrical frustration inherent to this lattice prevents magnetic order from forming down to the lowest temperatures. In contrast, the unit cell of Pb2CaOsO6 is heavily distorted up to at least 500 K, including antiferroelectric-like displacements of the Pb and O atoms despite metallic conductivity above 80 K. This distortion relieves the magnetic frustration, facilitating magnetic order which in turn drives the metal--insulator transition. Our results suggest that the phase transition in Pb2CaOsO6 is spin-driven, and could be a rare example of a Slater transition.

cond-mat.str-el↗

arXiv2020

Ferrimagnetic 120$^\circ$ magnetic structure in Cu2OSO4

We report magnetic properties of a 3d$^9$ (Cu$^{2+}$) magnetic insulator Cu2OSO4 measured on both powder and single crystal. The magnetic atoms of this compound form layers, whose geometry can be described either as a system of chains coupled through dimers or as a Kagomé lattice where every 3rd spin is replaced by a dimer. Specific heat and DC-susceptibility show a magnetic transition at 20 K, which is also confirmed by neutron scattering. Magnetic entropy extracted from the specific heat data is consistent with a $S=1/2$ degree of freedom per Cu$^{2+}$, and so is the effective moment extracted from DC-susceptibility. The ground state has been identified by means of neutron diffraction on both powder and single crystal and corresponds to a $\sim120$ degree spin structure in which ferromagnetic intra-dimer alignment results in a net ferrimagnetic moment. No evidence is found for a change in lattice symmetry down to 2 K. Our results suggest that \sample \ represents a new type of model lattice with frustrated interactions where interplay between magnetic order, thermal and quantum fluctuations can be explored.

cond-mat.str-el↗

arXiv2020

Realising square and diamond lattice $S=1/2$ Heisenberg antiferromagnet models in the $α$ and $β$ phases of the coordination framework, KTi(C$_2$O$_4$)$_2\cdot$\textit{x}H$_2$O

We report the crystal structures and magnetic properties of two psuedo-polymorphs of the $S=1/2$ Ti$^{3+}$ coordination framework, KTi(C$_2$O$_4$)$_2\cdot$xH$_2$O. Single-crystal X-ray and powder neutron diffraction measurements on $α$-KTi(C$_2$O$_4$)$_2\cdot$xH$_2$O confirm its structure in the tetragonal $I4/mcm$ space group with a square planar arrangement of Ti$^{3+}$ ions. Magnetometry and specific heat measurements reveal weak antiferromagnetic interactions, with $J_1\approx7$ K and $J_2/J_1=0.11$ indicating a slight frustration of nearest- and next-nearest-neighbor interactions. Below $1.8$ K, $α$ undergoes a transition to G-type antiferromagnetic order with magnetic moments aligned along the $c$ axis of the tetragonal structure. The estimated ordered moment of Ti$^{3+}$ in $α$ is suppressed from its spin-only value to $0.62(3)~μ_B$, thus verifying the two-dimensional nature of the magnetic interactions within the system. $β$-KTi(C$_2$O$_4$)$_2\cdot$2H$_2$O, on the other hand, realises a three-dimensional diamond-like magnetic network of Ti$^{3+}$ moments within a hexagonal $P6_222$ structure. An antiferromagnetic exchange coupling of $J\approx54$ K -- an order of magnitude larger than in $α$ -- is extracted from magnetometry and specific heat data. $β$ undergoes Néel ordering at $T_N=28$ K, with the magnetic moments aligned within the $ab$ plane and a slightly reduced ordered moment of $0.79~μ_B$ per Ti$^{3+}$. Through density-functional theory calculations, we address the origin of the large difference in the exchange parameters between the $α$ and $β$ psuedo-polymorphs. Given their observed magnetic behaviors, we propose $α$-KTi(C$_2$O$_4$)$_2\cdot$xH$_2$O and $β$-KTi(C$_2$O$_4$)$_2\cdot$2H$_2$O as close to ideal model $S=1/2$ Heisenberg square and diamond lattice antiferromagnets, respectively.

cond-mat.str-el↗

arXiv2020

Evolution of the structural, magnetic and electronic properties of the triple perovskite Ba$_{3}$CoIr$_{2}$O$_{9}$

We report a comprehensive investigation of the triple perovskite iridate Ba$_{3}$CoIr$_{2}$O$_{9}$. Stabilizing in the hexagonal $P6_{3}/mmc$ symmetry at room temperature, this system transforms to a monoclinic $C2/c$ symmetry at the magnetic phase transition. On further reduction in temperature, the system partially distorts to an even lower symmetry ($P2/c$), with both these structurally disparate phases coexisting down to the lowest measured temperatures. The magnetic structure as determined from neutron diffraction data indicates a weakly canted antiferromagnetic structure, which is also supported by first-principles calculations. Theory indicates that the Ir$^{5+}$ carries a finite magnetic moment, which is also consistent with the neutron data. This suggests that the putative $J=0$ state is avoided. Measurements of heat capacity, electrical resistance noise and dielectric susceptibility all point towards the stabilization of a highly correlated ground state in the Ba$_{3}$CoIr$_{2}$O$_{9}$ system.

cond-mat.str-el↗

arXiv2020

Unusual effects of magnetic dilution in the ferrimagnetic columnar ordered $\mathrm{Sm_2MnMnMn_{4-x}Ti_xO_{12}}$ perovskites

Powder neutron diffraction experiments have been employed to establish the effects of site-selective magnetic dilution in the Sm2MnMnMn4-x Tix O12 A-site columnar ordered quadruple perovskite manganites (x = 1, x = 2 and x = 3). We show that in all three compositions the Mn ions adopt a collinear ferrimagnetic structure below 27 K, 62 K and 34 K, respectively. An unexpected increase in the ordering temperature was observed between the x = 1 and x = 2 samples, which indicates a considerable departure from mean field behaviour. This result is corroborated by large reductions in the theoretical ground state magnetic moments observed across the series, which indicate the presence of spin fluctuations and or disorder. We show that long range magnetic order in the x = 3 sample, which occurs below the percolation threshold for B-B exchange, can only be understood to arise if magnetic order in Sm2MnMnMn4-xTixO12 is mediated via both A-B and B-B exchange, hence confirming the importance of A-B exchange interactions in these materials. Finally we show that site-selective magnetic dilution enables the tuning of a ferrimagnetic compensation point and the introduction of temperature-induced magnetization reversal.

cond-mat.str-el↗

arXiv2020

Nature of Partial Magnetic Order in the Frustrated Antiferromagnet Gd2Ti2O7

Partially-ordered magnets are distinct from both spin liquids and conventional ordered magnets because order and disorder coexist in the same magnetic phase. Here, we determine the nature of partial order in the canonical frustrated pyrochlore antiferromagnet Gd$_2$Ti$_{2}$O$_{7}$. Using single-crystal neutron-diffraction measurements in applied magnetic field, magnetic symmetry analysis, inelastic neutron-scattering measurements, and spin-wave modeling, we show that its low-temperature magnetic structure involves two propagation vectors (2-$\mathbf{k}$ structure) with suppressed ordered magnetic moments and enhanced spin-wave fluctuations. Our experimental results support theoretical predictions of thermal fluctuation-driven order in Gd$_{2}$Ti$_{2}$O$_{7}$.

cond-mat.str-el↗

arXiv2020

Emergent helical texture of electric dipoles

Long-range ordering of magnetic dipoles in bulk materials gives rise to a broad range of magnetic structures, from simple collinear ferromagnets and antiferromagnets, to complex magnetic helicoidal textures stabilized by competing exchange interactions. In contrast, in the context of dipolar order in dielectric crystals, only parallel (ferroelectric) and antiparallel (antiferroelectric) collinear alignments of electric dipoles are typically considered. Here, we report an observation of incommensurate helical ordering of electric dipoles by light hole-doping of the quadruple perovskite BiMn7O12. In analogy with magnetism, the electric dipole helicoidal texture is also stabilized by competing instabilities. Specifically, orbital ordering and lone electron pair stereochemical activity compete, giving rise to phase transitions from a non-chiral cubic structure, to an incommensurate electric dipole and orbital helix, via an intermediate density wave.

cond-mat.str-el↗

arXiv2020

Strengthening the magnetic interactions in pseudobinary first-row transition metal thiocyanates, $\it{M}$(NCS)$_{2}$

Understanding the effect of chemical composition on the strength of magnetic interactions is key to the design of magnets with stronger exchange interactions. The magnetic divalent first-row transition metal (TM) thiocyanates are a class of chemically simple layered molecular frameworks. Here, we report two new members of the family, manganese (II) thiocyanate, Mn(NCS)$_{2}$, and iron (II) thiocyanate, Fe(NCS)$_{2}$. Using magnetic susceptibility measurements on these materials and on cobalt (II) thiocyanate and nickel (II) thiocyanate, Co(NCS)$_{2}$ and Ni(NCS)$_{2}$, respectively, we identify significantly stronger net antiferromagnetic interactions between the earlier TM ions-a decrease in the Weiss constant, θ, from 29 K for Ni(NCS)$_{2}$ to -115 K for Mn(NCS)$_{2}$-a consequence of more diffuse 3d orbitals, increased orbital overlap and increasing numbers of unpaired $\it{t}$$_{2g}$ electrons. We elucidate the magnetic structures of these materials: Mn(NCS)$_{2}$, Fe(NCS)$_{2}$ and Co(NCS)$_{2}$ order into the same antiferromagnetic commensurate ground state, whilst Ni(NCS)$_{2}$ adopts a ground state structure consisting of ferromagnetically ordered layers stacked antiferromagnetically. We show that magnetic molecular frameworks with significantly stronger net exchange interactions can be constructed by using earlier TMs.

cond-mat.mtrl-sci↗