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Using a time-dependent density matrix renormalization group approach, we study the dynamical structure factor of the $J_1 - J_2$ spin-1 chain. As $J_2$ increases, the magnon mode develops incommensurability. The system undergoes a first-order transition at $J_2 = 0.76 J_1$, and at that point, domain walls lead to a continuum of fractional quasi-particles or spinons. By studying small variations in $J_2$ around the transition point, we observe the confinement of spinons into bound states in the spectral function and find a smooth evolution of the spectrum into magnon modes away from the phase transition. We employ the single-mode approximation to accurately account for the dispersion of the magnon mode away from the phase transition and describe the associated continua and bound states. We extend the single-mode approximation to describe the dispersion of a spinon at the phase transition point and obtain its dispersion throughout the Brillouin zone. This allows us to relate the incommensurability at and around the transition point to the competition between a negative nearest-neighbour hopping amplitude and a positive next-nearest-neighbour one for the domain wall., Comment: 16 pages, 13 Figures

We probe the spectrum of elementary excitations in SrIrO$_3$ by using heterostructured [(SrIrO$_3$)$_m$/(SrTiO$_3$)$_l$] samples to approach the bulk limit. Our resonant inelastic x-ray scattering (RIXS) measurements at the Ir $L_3$-edge reveal a robust low-lying collective magnetic mode with an antiferromagnetic (AF) dispersion similar to the insulators Sr$_2$IrO$_4$ and Sr$_3$Ir$_2$O$_7$, albeit with a large gap and much larger linewidth. At higher energies we find the spin-orbit exciton, also strongly broadened, but with an inverted dispersion and doubled periodicity that are controlled by the charge hopping. These results demonstrate that the AF paramagnon persists, somewhat counterintuitively, far into the metallic regime of the insulator-metal transition driven by the degree of confinement in the heterostructure. We conclude that these two excitations, which are contrasting but coexisting hallmarks of strong AF pseudospin and charge fluctuations in a spin-orbit-coupled Mott-Slater material, are properties intrinsic to the ground state of semimetallic perovskite SrIrO$_3$.

The simultaneous application of high magnetic fields and high pressures for controlling magnetic ground states is important for testing our understanding of many-body quantum theory. However, the implementation for neutron scattering experiments presents a technical challenge. To overcome this challenge we present an optimized pressure-cell design with a novel bullet shape, which is compatible with horizontal-field magnets, in particular the high-field magnet operating at the Helmholtz-Zentrum Berlin. The cell enabled neutron diffraction and spectroscopy measurements with the combination of three extreme conditions: high pressures, high magnetic fields, and dilution temperatures, simultaneously reaching 0.7 GPa, 25.9 T, and 200 mK. Our results demonstrate the utility of informed material choices and the efficiency of finite-element analysis for future pressure-cell designs to be used in combination with magnetic fields and dilution temperatures for neutron scattering purposes.

Quantum entanglement between the spin, orbital and lattice degrees of freedom in condensed matter systems can emerge due to an interplay between spin-orbit and vibronic interactions. Heavy transition metal ions decorated on a face-centered cubic lattice, for example in $5d^1$ double perovskites, are particularly suited to support these quantum entangled states, but direct evidence has not yet been presented. In this work, we report additional peaks in the low-energy spectra of a $5d^1$ double perovskite, Ba$_2$CaReO$_6$, which cannot be explained by adopting a purely classical description of lattice vibrations. Instead, our theoretical analysis demonstrates that these spectroscopic signatures are characteristic of orbital-lattice entangled states in Ba$_2$CaReO$_6$. Crucially, both theory and experiment demonstrate that these quantum-entangled states persist to low temperatures, despite the onset of multipolar order., Comment: 7 pages, 4 figures

Exotic quantum phases, arising from a complex interplay of charge, spin, lattice and orbital degrees of freedom, are of immense interest to a wide research community. A well-known example of such an entangled behavior is the Jahn-Teller effect, where the lifting of orbital degeneracy proceeds through lattice distortions, often accompanied by ordering of spins and metal-insulator transitions. Static distortions, including cooperative behavior, have been associated with colossal magneto-resistance, multiferroicity, high-$T_\mathrm{C}$ superconductivity and other correlated phenomena. Realizations of the dynamic Jahn-Teller effect, on the other hand, are scarce since the preservation of vibronic symmetries requires subtle tuning of the local environment. Here we demonstrate that a highly-symmetrical 5d$^1$ double perovskite Ba$_2$MgReO$_6$, comprising of a 3D array of isolated ReO$_6$ octahedra, fulfils these requirements, resulting in a unique case of a dynamic Jahn-Teller system with strong spin-orbit coupling. Thermodynamic and resonant inelastic x-ray scattering experiments undoubtedly show that the Jahn-Teller instability leads to a ground-state doublet, invoking a paradigm shift for this family of compounds. The restoration of vibronic degrees of freedom arises from a quantum-mechanical zero-point motion, as revealed by detailed quantum chemistry calculations. The dynamic state of ReO$_6$ octahedra persists down to the lowest temperatures, where a multipolar order sets in, allowing for investigations of the interplay between a dynamic JT effect and strongly correlated electron behavior.

In the rich phases of van der Waals (vdW) materials featuring intertwined electronic order and collective phenomena, characterizing elementary dynamics that entail the low-energy Hamiltonian and electronic degrees of freedom is of paramount importance. Here we performed resonant inelastic X-ray scattering (RIXS) to elaborate the spin-orbital ground and excited states of the vdW antiferromagnetic insulator FePS$_{3}$, as well as their relation to magnetism. We observed the spectral enhancement of spin-orbital multiplet transitions about $\sim$ 100 and $\sim$ 220 meV, as well as quasielastic response, when entering the zig-zag antiferromagnetic phase, where the spectral changes develop an order-parameter-like evolution with temperature. By comparing with ligand field theory calculations, we discovered the essential role of trigonal lattice distortion and negative metal-ligand charge-transfer to account for these emergent excitations. Such spectral profiles are further examined upon confinement by mechanical exfoliation. We reveal their spectral robustness down to the few atomic layer limit, in accordance with the persistent antiferromagnetic state previously reported in optical measurements. Our study demonstrates the versatile RIXS capability that resolves magneto-crystalline anisotropy and charge-transfer energetics. These provide the crucial insight to understand how the spontaneous magnetic symmetry-breaking stabilizes in the quasi-two-dimensional limit for the vdW magnet FePS$_{3}$.

Non-collinear magnetic skyrmion lattices provide novel magnonic functionalities due to their topological magnon bands and asymmetric dispersion relations. Magnon excitations with intermediate wavelengths comparable to inter-skyrmion distances are particularly interesting but largely unexplored so far due to experimental challenges. Here, we report the detection of such magnons with wavevectors q $\simeq$ 48 rad/um in the metastable skyrmion lattice phase of the bulk chiral magnet Cu$_2$OSeO$_3$ using micro-focused Brillouin light scattering microscopy. Thanks to its high sensitivity and broad bandwidth we resolved various excitation modes of a single skyrmion lattice domain over a wide magnetic field regime. Besides the known modes with dipole character, quantitative comparison of frequencies and spectral weights to theoretical predictions enabled the identification of a quadrupole mode and observation of signatures which we attribute to a decupole and a sextupole mode. Our combined experimental and theoretical work highlights that skyrmionic phases allow for the design of magnonic devices exploiting topological magnon bands.

The detection of inelastically scattered soft X-rays with high energy resolution usually requires large grating spectrometers. Recently, photoelectron spectrometry for analysis of X-rays (PAX) has been rediscovered for modern spectroscopy experiments at synchrotron light sources. By converting scattered photons to electrons and using an electron energy analyser, the energy resolution for resonant inelastic X-ray scattering (RIXS) becomes decoupled from the X-ray spot size and instrument length. In this work, we develop PAX towards high energy resolution using a modern photoemission spectroscopy setup studying Ba2Cu3O4Cl2 at the Cu L3-edge. We measure a momentum transfer range of 24% of the first Brillouin zone simultaneously. Our results hint at the observation of a magnon excitation below 100 meV energy transfer and show intensity variations related to the dispersion of dd-excitations. With dedicated setups, PAX can become an alternative to the best and largest RIXS instruments, while at the same time opening new opportunities to acquire RIXS at a range of momentum transfers simultaneously and combine it with angle-resolved photoemission spectroscopy in a single instrument.

Time and angle-resolved photoemission spectroscopy (trARPES) allows direct mapping of the electronic band structure and its dynamic response on femtosecond timescales. Here, we present a new ARPES system, powered by a new fiber-based femtosecond light source in the vacuum ultraviolet (VUV) range, accessing the complete first Brillouin zone for most materials. We present trARPES data on Au(111), polycrystalline Au, Bi2Se3 and TaTe2, demonstrating an energy resolution of 21 meV with a time resolution of <360 fs, at a high repetition rate of 1 MHz. The system is integrated with an extreme ultraviolet (EUV) high harmonic generation (HHG) beamline, enabling excellent tunability of the time-bandwidth resolution., Comment: The following article has been published in Review of Scientific Instruments. The article can be found at https://doi.org/10.1063/5.0179549

Clarifying the underlying mechanisms that govern ordering transitions in condensed matter systems is crucial for comprehending emergent properties and phenomena. While transitions are often classified as electronically driven or lattice-driven, we present a departure from this conventional paradigm in the case of the double perovskite Ba$_2$MgReO$_6$. Leveraging resonant and non-resonant elastic x-ray scattering techniques, we unveil the simultaneous ordering of structural distortions and charge quadrupoles at a critical temperature of $T_\mathrm{q}$$\sim$33 K. Using a variety of complementary first-principles-based computational techniques, we demonstrate that while electronic interactions drive the ordering at $T_\mathrm{q}$, it is ultimately the lattice that dictates the specific ground state that emerges. Our findings highlight the crucial interplay between electronic and lattice degrees of freedom, providing a unified framework to understand and predict unconventional emergent phenomena in quantum materials.

Quantum spin liquids are highly entangled magnetic states with exotic properties. The $S = 1/2$ square-lattice Heisenberg model is one of the foundational models in frustrated magnetism with a predicted, but never observed, quantum spin liquid state. Isostructural double perovskites Sr$_2$CuTeO$_6$ and Sr$_2$CuWO$_6$ are physical realizations of this model, but have distinctly different types magnetic order and interactions due to a $d^{10}/d^0$ effect. Long-range magnetic order is suppressed in the solid solution Sr$_2$CuTe$_{1-x}$W$_x$O$_6$ in a wide region of $x = 0.05-0.6$, where the ground state has been proposed to be a disorder-induced spin liquid. Here we show that the spin-liquid-like $x = 0.2$ and $x = 0.5$ samples have distinctly different local spin correlations, which suggests they have different ground states. Furthermore, the previously ignored interlayer coupling between the square-planes is likely to play a role in the suppression of magnetic order on the W-rich side at $x \approx 0.6$. These results highlight the complex magnetism of Sr$_2$CuTe$_{1-x}$W$_x$O$_6$ and hint at a new quantum critical point at $x \approx 0.3$., Comment: 19+8 pages, 6+8 figures

In the rapidly expanding field of topological materials there is growing interest in systems whose topological electronic band features can be induced or controlled by magnetism. Magnetic Weyl semimetals, which contain linear band crossings near the Fermi level, are of particular interest owing to their exotic charge and spin transport properties. Up to now, the majority of magnetic Weyl semimetals have been realized in ferro- or ferrimagnetically ordered compounds, but a disadvantage of these materials for practical use is their stray magnetic field which limits the minimum size of devices. Here we show that Weyl nodes can be induced by a helical spin configuration, in which the magnetization is fully compensated. Using a combination of neutron diffraction and resonant elastic x-ray scattering, we find that EuCuAs develops a planar helical structure below $T_\textrm{N}$ = 14.5 K which induces Weyl nodes along the $\Gamma$--A high symmetry line in the Brillouin zone.

We report the discovery of a novel skyrmion phase in the multiferroic insulator Cu2OSeO3 for magnetic fields below the equilibrium skyrmion pocket. This phase can be accessed by exciting the sample out of equilibrium with near-infrared (NIR) femtosecond laser pulses but can not be reached by any conventional field cooling protocol. From the strong wavelength dependence of the photocreation process and via spin dynamics simulations, we identify the magnetoelastic effect as the most likely photocreation mechanism. This effect results in a transient modification of the magnetic interaction extending the equilibrium skyrmion pocket to lower magnetic fields. Once created, the skyrmions rearrange and remain stable over a long time, reaching minutes. The presented results are relevant for designing high-efficiency non-volatile data storage based on magnetic skyrmions., Comment: 11 pages, 5 figures

We address magnetic neutron scattering in the presence of local non-centrosymmetric asymmetries of the magnetization density. Such inversion-symmetry breaking, combined with the absence of time-reversal symmetry, can be described in terms of magnetoelectric multipoles which form the second term after the magnetic dipole in the multipole expansion of the magnetization density. We provide a pedagogical review of the theoretical formalism of magnetic neutron diffraction in terms of the multipole expansion of the scattering cross-section. In particular, we show how to compute the contribution of magnetoelectric multipoles to the scattering amplitude starting from ab initio calculations. We also provide general guidelines on how to experimentally detect long-ranged order of magnetoelectric multipoles using either unpolarized or polarized neutron scattering. As a case study, we search for the presence of magnetoelectric multipoles in CuO by comparing theoretical first-principle predictions with experimental spherical neutron polarimetry measurements., Comment: 17 pages, 8 figures

We present a new method of Ba$_{2}$MgWO$_{6}$ single crystal synthesis that allows to grow larger crystals using BaCl$_{2}$ and MgCl$_{2}$ flux. Difficulties to grow single crystal of a size suitable for macroscopic material property measurements caused the majority of characterisation being published on polycrystalline samples. Single crystal diffraction and energy dispersive X-ray analysis confirmed high quality of synthesised samples. Heat capacity measurements from 300~K to 2~K do not show any transitions. However, Raman spectra measured down to 77~K contain additional peaks at all temperatures probed, which is in a contrast with only 4 Raman active modes expected from the reducible representation. This calls for a more detailed study of potential symmetry breaking that could also influence the electronic properties of the material.

Dark blue single crystals of Al$_{1.75}^{3+}$ Ti$_{1.0}^{4+}$ Ti$_{0.25}^{3+}$O$_5$ were grown with a novel synthesis method based on the reaction of a Ti3+/Ti4+ containing langbeinite melt and Al$_2$O$_3$. The obtained needles crystallize in the pseudobrookite structure and undergo two reversible phase transitions from orthorhombic Cmcm to C2/m first and subsequently to C2 symmetry. Like the known aluminum titanate pseudobrookites, anistropic thermal expansion is observed. The temperature evolution of the crystal structure reveals some insights into the mechanism leading to the decomposition of the Al$_{1.75}$Ti$_{1.25}$O$_5$ above 725$^\circ$C. The magnetic and electrical properties are discussed and compared to other reported aluminum titanate pseudobrookites., Comment: 5 figures in the main text

Recent discovery of topologically non-trivial behavior in Co3Sn2S2 stimulated a notable interest in this itinerant ferromagnet (Tc = 174 K). The exact magnetic state remains ambiguous, with several reports indicating the existence of a second transition in the range 125 -- 130 K, with antiferromagnetic and glassy phases proposed to coexist with the ferromagnetic phase. Using detailed angle-dependent DC and AC magnetization measurements on large, high-quality single crystals we reveal a highly anisotropic behavior of both static and dynamic response of Co3Sn2S2. It is established that many observations related to sharp magnetization changes when B || c are influenced by the demagnetization factor of a sample. On the other hand, a genuine transition has been found at Tp = 128 K, with the magnetic response being strictly perpendicular to the c-axis and several orders of magnitude smaller than for B || c. Calculations using density-functional theory indicate that the ground state magnetic structure consist of magnetic moments canted away from the c-axis by a small angle (~ 1.5deg). We argue that the second transition originates from a small additional canting of moments within the kagome plane, with two equivalent orientations for each spin., Comment: accepted as a Letter in PRB

We address the degeneracy of the ground state multiplet on the 5$d^1$ Re$^{6+}$ ion in double perovskite Ba$_{2}$MgReO$_{6}$ using a combination of specific heat measurements and density functional calculations. For Ba$_{2}$MgReO$_{6}$, two different ground state multiplets have previously been proposed - a quartet (with degeneracy $N$=4) [1] and a doublet ($N$=2) [2]. Here we employ two independent methods for the estimation of phonon contribution in heat capacity data to obtain the magnetic entropy $S_{mag}$, which reflects the degeneracy of the ground state multiplet $N$ through $S_{mag}=R$ln$N$. In both cases, we obtain a better fit to $S_{mag}=R$ln2 indicating evidence of $N$=2 degeneracy in the range from 2 to 120~K. The detailed nature of the ground state multiplet in Ba$_{2}$MgReO$_{6}$ remains an open question., Comment: 5 pages, 4 figures

Control of magnetization and electric polarization is attractive in relation to tailoring materials for data storage and devices such as sensors or antennae. In magnetoelectric materials, these degrees of freedom are closely coupled, allowing polarization to be controlled by a magnetic field, and magnetization by an electric field, but the magnitude of the effect remains a challenge in the case of single-phase magnetoelectrics for application. We demonstrate that the magnetoelectric properties of the mixed-anisotropy antiferromagnet LiNi$_{1-x}$Fe$_x$PO$_4$ are profoundly affected by replacing a fraction of the Ni$^{2+}$ ions with Fe$^{2+}$ on the transition metal site. This introduces random site-dependent single-ion anisotropy energies and causes a lowering of the magnetic symmetry of the system. In turn, magnetoelectric couplings that are symmetry-forbidden in the parent compounds, LiNiPO$_4$ and LiFePO$_4$, are unlocked and the dominant coupling is enhanced by two orders of magnitude. Our results demonstrate the potential of mixed-anisotropy magnets for tuning magnetoelectric properties.

Dynamical perturbations modify the states of classical systems in surprising ways and give rise to important applications in science and technology. For example, Floquet engineering exploits the possibility of band formation in the frequency domain when a strong, periodic variation is imposed on parameters such as spring constants. We describe here Kapitza engineering, where a drive field oscillating at a frequency much higher than the characteristic frequencies for the linear response of a system changes the potential energy surface so much that maxima found at equilibrium become local minima, in precise analogy to the celebrated Kapitza pendulum where the unstable inverted configuration, with the mass above rather than below the fulcrum, actually becomes stable. Our starting point is a quantum field theory of the Ginzburg-Devonshire type, suitable for many condensed matter systems, including particularly ferroelectrics and quantum paralectrics. We show that an off-resonance oscillatory electric field generated by a laser-driven THz source can induce ferroelectric order in the quantum-critical limit. Heating effects are estimated to be manageable using pulsed radiation; ``hidden" radiation-induced order can persist to low temperatures without further pumping due to stabilization by strain. We estimate the Ginzburg-Devonshire free-energy coefficients in SrTiO${}_{3}$ using density-functional theory (DFT) and the stochastic self-consistent harmonic approximation accelerated by a machine-learned force field. Although we find that SrTiO${}_{3}$ is not an optimal choice for Kapitza stabilization, we show that scanning for further candidate materials can be performed at the computationally convenient density-functional theory level. We suggest second-harmonic-generation, soft-mode-spectroscopy, and X-ray-diffraction experiments to characterize the induced order., Comment: 9+4 pages, 5+2 figures, submitted to Physical Review X

We examine the role of charge, structural, and spin degrees of freedom in the previously poorly understood phase transition in the 5$d^1$ transition-metal double perovskite Cs$_2$TaCl$_6$, using a combination of computational and experimental techniques. Our heat capacity measurements of single-crystalline Cs$_2$TaCl$_6$, reveal a clear anomaly at the transition temperature, $T_\mathrm{Q}$, which was not previously observed in polycrystalline samples. Density functional calculations indicate the emergence of local charge quadrupoles in the cubic phase, mediated by the paramagnetic spins or local structural distortions which then develop into long-range ordered charge quadrupoles in the tetragonal phase. Our resonant elastic x-ray scattering on Cs$_2$TaCl$_6$, single crystals lend support to our calculations. Our work provides new insight into the phase transition in Cs$_2$TaCl$_6$, at $T_\mathrm{Q}$, and demonstrates the utility of this combination of techniques in understanding the complex physics of hidden orders in paramagnetic spin-orbit-entangled compounds.

The magnetic, dielectric and structural properties of type-I multiferroic KNiPO$_4$ have been investigated by neutron powder diffraction, magnetization, dielectric and high temperature synchrotron-XRD measurements. Below the N\'{e}el transition of $T_\mathrm{N}$ = 25 K, KNiPO$_4$ displays a weakly non-collinear antiferromagnetic (AFM) structure with the orientation of the Ni$^{2+}$ magnetic moments mainly along $a$ axis. The compound crystallizes in the polar orthorhombic $Pna2_1$ space group at room temperature. A second-order structural phase transition corresponding to the onset ferroelectricity is observed at around $T_\mathrm{C}\sim$ 594(3)$^\circ$C, above which the crystal structure of KNiPO$_4$ adopts the centrosymmetric $Pnma$ space group. The compound also displays another structural phase transition at $T_\mathrm{0}\sim$ 469 -- 488$^\circ$C, with a first-order character, which is attributed to the rearrangement of oxygen ligands, resulting in a change in the nickel ion co-ordination from four to five.

Topological spin textures such as skyrmions hold high potential for use as magnetically active elements in diverse near-future applications. While skyrmions in metallic multilayers attract great attention in this context, unleashing the myriad potential of skyrmions for various applications requires the discovery and customization of alternative host system paradigms. Here we developed and applied a chemical method to synthesize octahedral particles of the chiral insulating skyrmion host Cu2OSeO3 with both narrow size distribution, and tailored dimensions approaching the nanoscale. Combining magnetometry and neutron scattering experiments with micromagnetic simulations, we show that the bulk phase diagram of Cu2OSeO3 changes dramatically below octahedral heights of 400 nm. Further particle size-dependent regimes are identified where various topological spin textures such as skyrmions, merons and bobbers can stabilize, prior to a lower critical octahedral height of approx. 190 nm below which no topological spin texture is found stable. These findings suggest conditions under which sparse topological spin textures confined to chiral magnet nanoparticles can be stable, and provide fresh potential for insulator-based application paradigms.

We investigate the prospect of achieving negative permittivity and permeability at optical frequencies in a dielectric crystal containing stoichiometric rare-earth ions. We derive the necessary transition linewidth, ion density and electric and magnetic oscillator strengths using a simplified model of non-interacting dipoles. We identify Erbium crystals in a magnetically ordered phase as the most promising material to meet these conditions, and describe initial optical measurements of two potential candidates, \ercl{} and ${}^7$\lierf{}, which display linewidths of 3~GHz and 250~MHz, respectively. The properties of ${}^7$\lierf{} satisfied our criterion for negative permeability.

We report high-resolution single-crystal inelastic neutron scattering measurements on the spin-1/2 antiferromagnet Ba(TiO)Cu$_4$(PO$_4$)$_4$. This material is formed from layers of four-site \cupola" structures, oriented alternately upwards and downwards, which constitute a rather special realization of two-dimensional (2D) square-lattice magnetism. The strong Dzyaloshinskii-Moriya (DM) interaction within each cupola, or plaquette, unit has a geometry largely unexplored among the numerous studies of magnetic properties in 2D Heisenberg models with spin and spatial anisotropies. We have measured the magnetic excitations at zero field and in fields up to 5 T, finding a complex mode structure with multiple characteristic features that allow us to extract all the relevant magnetic interactions by modelling within the linear spin-wave approximation. We demonstrate that Ba(TiO)Cu$_4$(PO$_4$)$_4$ is a checkerboard system with almost equal intra- and inter-plaquette couplings, in which the intra-plaquette DM interaction is instrumental both in enforcing robust magnetic order and in opening a large gap at the Brillouin-zone center. We place our observations in the perspective of generalized phase diagrams for spin-1/2 square-lattice models and materials, where exploring anisotropies and frustration as routes to quantum disorder remains a frontier research problem., Comment: 13 pages, 8 figures

We explore the interplay between randomness and magnetic frustration in the series of $S = 1/2$ Heisenberg square-lattice compounds Sr$_2$CuTe$_{1-x}$W$_x$O$_6$. Substituting W for Te alters the magnetic interactions dramatically, from strongly nearest-neighbor to next-nearest-neighbor antiferromagnetic coupling. We perform neutron scattering measurements to probe the magnetic ground state and excitations over a range of $x$. We propose a bond-disorder model that reproduces ground states with only short-ranged spin correlations in the mixed compounds. The calculated neutron diffraction patterns and powder spectra agree well with the measured data and allow detailed predictions for future measurements. We conclude that quenched randomness plays the major role in defining the physics of Sr$_2$CuTe$_{1-x}$W$_x$O$_6$ with frustration being less significant.

We present first principles calculations of the dynamic susceptibility in strained and doped ferromagnetic MnBi using time-dependent density functional theory. In spite of being a metal, MnBi exhibits signatures of strong correlation and a proper description in the framework of density functional theory requires Hubbard corrections to the Mn $d$-orbitals. To permit calculations of the dynamic susceptibility with Hubbard corrections applied to the ground state electronic structure, we use a consistent rescaling of the exchange-correlation kernel maintaining the delicate balance between the magnon dispersion and the Stoner continuum. We find excellent agreement with the experimentally observed magnon dispersion for pristine MnBi and show that the material undergoes a phase transition to helical order under application of either doping or strain. The presented methodology paves the way for future LR-TDDFT studies of magnetic phase transitions, also for the wide range of materials with pronounced static correlation effects that are not accounted for at the LDA level., Comment: 14 pages, v2

Exotic magnetic textures emerging from the subtle interplay between thermodynamic and topological fluctuation have attracted intense interest due to their potential applications in spintronic devices. Recent advances in electron microscopy have enabled the imaging of random photo-generated individual skyrmions. However, their deterministic and dynamical manipulation is hampered by the chaotic nature of such fluctuations and the intrinsically irreversible switching between different minima in the magnetic energy landscape. Here, we demonstrate a method to coherently control the rotation of a skyrmion crystal by discrete amounts at speeds which are much faster than previously observed. By employing circularly polarized femtosecond laser pulses with an energy below the bandgap of the Mott insulator Cu2OSeO3, we excite a collective magnon mode via the inverse Faraday effect. This triggers coherent magnetic oscillations that directly control the rotation of a skyrmion crystal imaged by cryo-Lorentz Transmission Electron Microscopy. The manipulation of topological order via ultrafast laser pulses shown here can be used to engineer fast spin-based logical devices.

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., Comment: accepted in PRL

In condensed matter systems, the atoms, electrons or spins can sometimes arrange themselves in ways that result in unexpected properties but that cannot be detected by conventional experimental probes. Several historical and contemporary examples of such hidden orders are known and more are awaiting discovery, perhaps in the form of more complex composite, entangled or dynamical hidden orders., Comment: Author Accepted Manuscript

The magnetic and structural properties of polycrystalline Co$_{4-x}$ Ni$_x$ Nb$_2$ O$_9$ (x=1,2) have been investigated by neutron powder diffraction, magnetization and heat capacity measurements, and density functional theory (DFT) calculations. For x=1, the compound crystallizes in the trigonal P$\bar{3}$c1 space group. Below T$_N$ = 31 K it develops a weakly non-collinear antiferromagnetig structure with magnetic moments in the ab-plane. The compound with x=2 has crystal structure of the orthorhombic Pbcn space group and shows a hard ferrimagnetic behavior below T$_C$ =47 K. For this compound a weakly non-collinear ferrimagnetic structure with two possible configurations in ab plane was derived from ND study. By calculating magnetic anisotropy energy via DFT, the ground-state magnetic configuration was determined for this compound. The heat capacity study in magnetic fields up to 140 kOe provide further information on the magnetic structure of the compounds., Comment: Published in Physical Review B, 8 pages, 8 figures

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 Kagom\'e 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., Comment: Published in Physical Review B

The discovery of multiple coexisting magnetic phases in a crystallographically homogeneous compound Ca$_3$Co$_2$O$_6$ has stimulated an ongoing research activity. In recent years the main focus has been on the zero field state properties, where exceedingly long time scales have been established. In this study we report a detailed investigation of static and dynamic properties of Ca$_3$Co$_2$O$_6$ across the magnetic field induced transition around 3.5 T. This region has so far been practically neglected while we argue that in some aspects it represents a simpler version of the transition across the $B = 0$ state. Investigating the frequency dependence of the ac susceptibility we reveal that on the high field side ($B > 3.5$ T) the response corresponds to a relatively narrow distribution of magnetic clusters. The distribution appears very weakly dependent on magnetic field, with an associated energy barrier of around 200 K. Below 3.5 T a second contribution arises, with much smaller characteristic frequencies and a strong temperature and magnetic field dependence. We discuss these findings in the context of intra-chain and inter-chain clustering of magnetic moments., Comment: accepted in PRB

We report on the commissioning results of the cold neutron multiplexing secondary spectrometer CAMEA (\textbf{C}ontinuous \textbf{A}ngle \textbf{M}ulti-\textbf{E}nergy \textbf{A}nalysis) at the Swiss Spallation Neutron Source (SINQ) at the Paul Scherrer Institut, Switzerland. CAMEA is optimized for an efficient data acquisition of scattered neutrons in the horizontal scattering plane, allowing for detailed and rapid mapping of low-energy excitations under extreme sample environment conditions.

Transition-metal dichalcogenides (TMDs) are layered compounds that support many electronic phases, including various charge density waves, superconducting, and Mott insulating states. Their intercalation with magnetic ions introduces magnetic sublayers, which strongly influence the coupling between host layers, and feature various magnetic states adjustable by external means. Co$_{1/3}$NbS$_2$ hosts a particularly sensitive magnetic subsystem with the lowest magnetic ordering temperature in the family of magnetically intercalated TMDs, and the only one where the complete suppression of magnetic order under pressure has been recently suggested. By combining the results of several experimental methods, electronic ab initio calculations, and modeling, we develop insights into the mechanisms of electric transport, magnetic ordering, and their interaction in this compound. The elastic neutron scattering is used to directly follow the evolution of the antiferromagnetic order parameter with pressure and temperature. Our results unambiguously disclose the complete suppression of the observed magnetic order around 1.7 GPa. We delve into possible mechanisms of magnetic order suppression under pressure, highlighting the role of magnetic frustrations indicated by magnetic susceptibility measurements and ab-initio calculations. Electronic conduction anisotropy is measured in the wide temperature and pressure range. Here we show that the transport in directions along and perpendicular to layers respond differently to the appearance of magnetic ordering or the application of the hydrostatic pressure. We propose the 'spin-valve' mechanism where the intercalated Co ions act as spin-selective electrical transport bridges between host layers. The mechanism applies to various magnetic states and can be extended to other magnetically intercalated TMDs., Comment: 36 pages, 19 figures

In the Ca$_{1-x}$La$_x$FeAs$_2$ (112) family of pnictide superconductors, we have investigated a highly overdoped composition (x = 0.56), prepared by high-pressure, high-temperature synthesis. Magnetic measurements show an antiferromagnetic transition at TN = 120K, well above the one at lower doping (0.15 < x < 0.27). Below the onset of long-range magnetic order at TN, the electrical resistivity is strongly reduced and is dominated by electron-electron interactions, as evident from its temperature dependence. The Seebeck coefficient shows a clear metallic behavior as in narrow band conductors. The temperature dependence of the Hall coefficient and the violation of Kohler's rule agree with the multiband character of the material. No superconductivity was observed down to 1.8 K. The success of the high-pressure synthesis encourages further investigations of the so far only partially explored phase diagram in this family of Iron-based high temperature superconductors.

Chiral magnetic textures with non-trivial topology are known as skyrmions, and due to their unique properties they are promising in novel magnetic storage applications. While the electric manipulation of either isolated skyrmions or a whole skyrmion lattice have been intensively reported, the electric effects on skyrmion clusters remain scarce. In magnetoelectric compound Cu$_2$OSeO$_3$, a skyrmion cluster can be created near the helical-skyrmion phase boundary. Here, we report the in situ electric field writing/erasing of skyrmions in such a skyrmion cluster. Our real space/time image data obtained by Lorentz transmission electron microscopy and the quantitative analysis evidence the linear increase of the number of skyrmions in the cluster upon the application of a creating electric field. The energy needed to create a single skyrmion is estimated to be $\mathcal{E}=4.7 \times 10^{-24}$ J.

Skyrmions are twirling magnetic textures whose non-trivial topology leads to particle-like properties promising for information technology applications. Perhaps the most important aspect of interacting particles is their ability to form thermodynamically distinct phases from gases and liquids to crystalline solids. Dilute gases of skyrmions have been realized in artificial multilayers, and solid crystalline skyrmion lattices have been observed in bulk skyrmion hosting materials. Yet, to date melting of the skyrmion lattice into a skyrmion liquid has not been reported experimentally. Through direct imaging with cryo-Lorentz transmission electron microscopy, we demonstrate that the skyrmion lattice in the material Cu$_2$OSeO$_3$ can be dynamically melted. Remarkably, we discover this melting process to be a topological defects mediated two-step transition via a theoretically hypothesized hexatic phase to the liquid phase. The existence of hexatic and liquid phases instead of a simple fading of the local magnetic moments upon thermal excitations implies that even in bulk materials skyrmions possess considerable particle nature, which is a pre-requisite for application schemes.

We present an experimental investigation of the magnetic structure in a tetramer system SeCuO$_3$ using neutron diffraction and nuclear resonance techniques. We establish a non-collinear, commensurate antiferromagnetic ordering with a propagation vector $\textbf{k} = \left(0,0,1 \right)$. The order parameter follows a critical behavior near $T_N = 8$ K, with a critical exponent $\beta = 0.32$ in agreement with a 3D universality class. Evidence is presented that a singlet state starts to form on tetramers at temperatures as high as 200 K, and its signature is preserved within the ordered state through a strong renormalization of the ordered magnetic moment on two non-equivalent copper sites, $m_{Cu1} \approx 0.4 \mu_B$ and $m_{Cu2} \approx 0.7 \mu_B$ at 1.5 K.

Resonant inelastic X-ray scattering (RIXS) experiments performed at the oxygen-$K$ edge on the iridate perovskites {\SIOS} and {\SION} reveal a sequence of well-defined dispersive modes over the energy range up to $\sim 0.8$ eV. The momentum dependence of these modes and their variation with the experimental geometry allows us to assign each of them to specific collective magnetic and/or electronic excitation processes, including single and bi-magnons, and spin-orbit and electron-hole excitons. We thus demonstrated that dispersive magnetic and electronic excitations are observable at the O-$K$ edge in the presence of the strong spin-orbit coupling in the $5d$ shell of iridium and strong hybridization between Ir $5d$ and O $2p$ orbitals, which confirm and expand theoretical expectations. More generally, our results establish the utility of O-$K$ edge RIXS for studying the collective excitations in a range of $5d$ materials that are attracting increasing attention due to their novel magnetic and electronic properties. Especially, the strong RIXS response at O-$K$ edge opens up the opportunity for investigating collective excitations in thin films and heterostructures fabricated from these materials., Comment: 6 pages, 4 figures with supplementary material. Accepted by PRB Rapid Communications