arXiv subjects

Karin Schmalzl

Publications and source records attributed to Karin Schmalzl.

16 recordsLinked to original sources

arXiv2026

Tilted and Twisted Magnetic Moments in the Kitaev Magnet $α$-RuCl$_3$

The layered honeycomb magnet $α$-RuCl$_3$ has attracted intense scrutiny as a prime candidate for realizing the Kitaev quantum spin liquid, yet a consensus on its microscopic Hamiltonian remains elusive due to the material's extreme sensitivity to structural details. Here, we report a comprehensive reexamination of the low-temperature crystallographic and magnetic structures of high-quality $α$-RuCl$_3$ single crystals using unpolarized and polarized neutron diffraction. We confirm a sharp, first-order structural phase transition to the rhombohedral $R\bar{3}$ space group with a pronounced thermal hysteresis. Crucially, using both spherical and longitudinal neutron polarization analysis, we determine the 3D orientation of the ordered magnetic moment without the ambiguity typically arising from domain distributions. We find that the Ru$^{3+}$ magnetic moments in the zigzag phase are tilted by $15.7^\circ$ out of the hexagonal plane and, remarkably, exhibit an additional in-plane twist of $-13.8^\circ$. This "tilted and twisted" geometry differentiates the ground state from the previously reported models based on unpolarized neutron diffraction or resonant elastic X-ray scattering (REXS) analysis.

cond-mat.str-el↗

arXiv2026

Non-reciprocal spin excitations across the skyrmion-paramagnetic phase transition in MnSi

The magnetic excitations of the skyrmion lattice in MnSi comprise a multitude of individual modes, which are non-reciprocal and thereby propagate unidirectionally. We report inelastic neutron scattering experiments for temperatures near and above the skyrmion-paramagnetic phase transition in the chiral magnet MnSi tracking the evolution from the skyrmion lattice towards the high-temperature paramagnetic state. Within the resolution of the triple-axis measurements the excitations vary smoothly across the skyrmion-paramagnetic boundary, and, the quasi-elastic paramagnetic signal under applied field retains the non-reciprocal character seen in the skyrmion phase even far above the critical temperature. Using a resolution-convolution our results are consistent with linear spin-wave theory.

cond-mat.str-el↗

arXiv2025

Giant Magnetocaloric Effect in Spin Supersolid Candidate Na$_2$BaCo(PO$_4$)$_2$

Supersolid, an exotic quantum state of matter that consists of particles forming an incompressible solid structure while simultaneously showing superfluidity of zero viscosity [1], is one of the long-standing pursuits in fundamental research [2, 3]. Although the initial report of $^4$He supersolid turned out to be an artifact [4], this intriguing quantum matter has inspired enthusiastic investigations into ultracold quantum gases [5-8]. Nevertheless, the realization of supersolidity in condensed matter remains elusive. Here we find evidence for a quantum magnetic analogue of supersolid -- the spin supersolid -- in the recently synthesized triangular-lattice antiferromagnet Na$_2$BaCo(PO$_4$)$_2$ [9]. Notably, a giant magnetocaloric effect related to the spin supersolidity is observed in the demagnetization cooling process, manifesting itself as two prominent valley-like regimes, with the lowest temperature attaining below 100 mK. Not only is there an experimentally determined series of critical fields but the demagnetization cooling profile also shows excellent agreement with the theoretical simulations with an easy-axis Heisenberg model. Neutron diffractions also successfully locate the proposed spin supersolid phases by revealing the coexistence of three-sublattice spin solid order and interlayer incommensurability indicative of the spin superfluidity. Thus, our results indicate a strong entropic effect of the spin supersolid phase in a frustrated quantum magnet and open up a viable and promising avenue for applications in sub-Kelvin refrigeration, especially in the context of persistent concerns about helium shortages [10, 11].

cond-mat.str-el↗

arXiv2024

Ground-state magnetic structures of topological kagome metals RV$_6$Sn$_6$ (R = Tb, Dy, Ho, Er)

Magnetic kagome metals have attracted tremendous research interests recently, because they represent an ideal playground for exploring the fascinating interplay between their intrinsically inherited topologically non-trivial electron band structures, magnetism and electronic correlation effects, and the resultant novel electronic/magnetic states and emergent excitations. In this work, we report a comprehensive single-crystal neutron diffraction investigation of the ground-state magnetic structures of the recently discovered V-based topological kagome metals RV$_6$Sn$_6$ (R = Tb, Dy, Ho, Er). Furthermore, the sample synthesis details and our systematic studies of crystal structure, low-temperature magnetic and thermodynamic properties of these compounds via various in-house characterization techniques are also reported. It can be revealed that RV$_6$Sn$_6$ (R = Tb, Dy, Ho) have a collinear ferromagnetic order in the ground state, with the ordered magnetic moment aligned along the c axis for R = Tb, Ho, while approximately 20${^\circ}$ tilted off from the c axis for R = Dy. In contrast, ErV$_6$Sn$_6$ shows an A-type antiferromagnetic structure with a magnetic propagation vector k = (0, 0, 0.5), and with the ordered magnetic moment aligned in the ab plane. A comparison of the low-temperature magnetic structures for both the extensively investigated topological kagome metal series of RV$_6$Sn$_6$ and RMn$_6$Sn$_6$ is given in details. This allows to gain new insights into the complex magnetic interactions, diverse single-ion magnetic anisotropies and spin dynamics in these compounds. The reported ground-state magnetic structures in RV$_6$Sn$_6$ (R = Tb, Dy, Ho, Er) can pave the way for further explorations of the possible interplay between magnetism and topologically non-trivial electron band structures in the magnetically ordered phase regime.

cond-mat.str-el↗

arXiv2024

Crystal structure and absence of magnetic order in single crystalline RuO$_2$

RuO$_2$ was considered for a long time to be a paramagnetic metal with an ideal rutile-type structure down to low temperatures, but recent studies on single-crystals claimed evidence for antiferromagnetic order and some symmetry breaking in the crystal structure. We have grown single-crystals of RuO2 by vapor transport using either O$_2$ or TeCl$_4$ as transport medium. These crystals exhibit metallic behavior following a $T^2$ low-temperature relation and a small paramagnetic susceptibility that can be attributed to Pauli paramagnetism. Neither the conductance nor the susceptibility measurements yield any evidence for a magnetic or a structural transition between 300K and $\sim$4 K. Comprehensive single-crystal diffraction studies with neutron and X-ray radiation reveal the rutile structure to persist until 2K in our crystals, and show nearly perfect stoichiometry. Previous observations of symmetry forbidden reflections can be attributed to multiple diffraction. Polarized single-crystal neutron diffraction experiments at 1.6K exclude the proposed antiferromagnetic structures with ordered moments larger than 0.01 Bohr magnetons.

cond-mat.mtrl-sci↗

arXiv2023

Multiferroic domain relaxation in (NH4)2[FeCl5(H2O)]

The molecular compound (NH4)2[FeCl5(H2O)] is a type-II multiferroic material, in which incommensurate cycloidal order directly induces ferroelectric polarization. The multiferroic domain kinetics in (NH4)2[FeCl5(H2O)] were studied by time-resolved neutron diffraction experiments utilizing neutron polarization analysis. The temperature and electric-field dependent multiferroic relaxation obeys the simple combined Arrhenius-Merz law, which was reported to describe domain kinetics in the prototype multiferroics TbMnO3 and NaFeGe2O6. However, the characteristic time scale of the multiferroic relaxation is considerably larger than those in TbMnO3 or NaFeGe2O6. Temperature-dependent diffraction on (NH4)2[FeCl5(H2O)] reveals the emergence of higher-order and commensurate magnetic contributions upon cooling in the multiferroic phase in zero field. The good agreement with studies of higher-harmonic contributions in the deuterated material indicates that the isotopes only posses a minor impact on the magnetic ordering. But in contrast to similar observations in multiferroic MnWO4, this anharmonic modification of magnetic ordering does not depin multiferroic domain walls or alter the temperature dependence of the multiferroic relaxation.

cond-mat.str-el↗

arXiv2023

Spin dynamics of the $E_8$ particles

In this article, we report on inelastic neutron scattering measurements on a quasi-1D antiferromagnet BaCo$_2$V$_2$O$_8$ under a transverse magnetic field applied along the (0,1,0) direction. Combining results of inelastic neutron scattering experiments, analytical analysis, and numerical simulations, we precisely studied the $E_8$ excitations appearing in the whole Brillouin zone at $B_c^{1D}\approx 4.7$ T. The energy scan at $Q=(0,0,2)$ reveals a match between the data and the theoretical prediction of energies of multiple $E_8$ excitations. Furthermore, dispersions of the lightest three $E_8$ particles have been clearly observed, confirming the existence of the $E_8$ particles in BaCo$_2$V$_2$O$_8$. Our results lay down a concrete ground to systematically study the physics of the exotic $E_8$ particles.

cond-mat.str-el↗

arXiv2023

Flat band-engineered spin-density wave and the emergent multi-$k$ magnetic state in the topological kagome metal Mn$_{3}$Sn

Magnetic kagome metals, in which topologically non-trivial band structures and electronic correlation are intertwined, have recently emerged as an exciting platform to explore exotic correlated topological phases, that are usually not found in weakly interacting materials described within the semi-classical picture of electrons. Here, via a comprehensive single-crystal neutron diffraction and first-principles density functional theory study of the archetypical topological kagome metal Mn$_3$Sn, which is also a magnetic Weyl fermion material and a promising chiral magnet for antiferromagnetic spintronics, we report the realisation of an emergent spin-density wave (SDW) order, a hallmark correlated many-body phenomenon, that is engineered by the Fermi surface nesting of topological flat bands. We further reveal that the phase transition, from the well-known high-temperature coplanar and non-collinear k = 0 inverse triangular antiferromagnetic order to a double-$k$ non-coplanar modulated incommensurate magnetic structure below $T_1$ = 280 K, is primarily driven by the SDW instability. The double-$k$ nature of this complex low-temperature magnetic order, which can be regarded as an intriguing superposition of a longitudinal SDW with a modulation wavevector k$_L$ and a transverse incommensurate helical magnetic order with a modulation wavevector k$_T$, is unambiguously confirmed by our observation of the inter-modulation high-order harmonics of the type of 2k$_L$+k$_T$. This discovery not only solves a long-standing puzzle concerning the nature of the phase transition at $T_1$, but also provides an extraordinary example on the intrinsic engineering of correlated many-body phenomena in topological matter. The identified multi-$k$ magnetic state can be further exploited for the engineering of the new modes of magnetization and chirality switching in antiferromagnetic spintronics.

cond-mat.str-el↗

arXiv2021

Topological magnon insulators in two-dimensional van der Waals ferromagnets CrSiTe$_3$ and CrGeTe$_3$: towards intrinsic gap-tunability

The bosonic analogues of topological insulators have been proposed in numerous theoretical works, but their experimental realization is still very rare, especially for spin systems. Recently, two-dimensional (2D) honeycomb van der Waals (vdW) ferromagnets have emerged as a new platform for topological spin excitations. Here, via a comprehensive inelastic neutron scattering study and theoretical analysis of the spin-wave excitations, we report the realization of topological magnon insulators in CrXTe$_3$ (X=Si, Ge) compounds. The nontrivial nature and intrinsic tunability of the gap opening at the magnon band-crossing Dirac points are confirmed, while the emergence of the corresponding in-gap topological edge states is demonstrated theoretically. The realization of topological magnon insulators with intrinsic gap-tunability in this class of remarkable 2D materials will undoubtedly lead to new and fascinating technological applications in the domain of magnonics and topological spintronics.

cond-mat.str-el↗

arXiv2020

In-plane uniaxial pressure-induced out-of-plane antiferromagnetic moment and critical fluctuations in BaFe$_2$As$_2$

A small in-plane external uniaxial pressure has been widely used as an effective method to acquire single domain iron pnictide BaFe$_2$As$_2$, which exhibits twin-domains without uniaxial strain below the tetragonal-to-orthorhombic structural (nematic) transition temperature $T_s$. Although it is generally assumed that such a pressure will not affect the intrinsic electronic/magnetic properties of the system, it is known to enhance the antiferromagnetic (AF) ordering temperature $T_N$ ($<T_s$) and create in-plane resistivity anisotropy above $T_s$. Here we use neutron polarization analysis to show that such a strain on BaFe$_2$As$_2$ also induces a static or quasi-static out-of-plane ($c$-axis) AF order and its associated critical spin fluctuations near $T_N/T_s$. Therefore, uniaxial pressure necessary to detwin single crystals of BaFe$_2$As$_2$ actually rotates the easy axis of the collinear AF order near $T_N/T_s$, and such effect due to spin-orbit coupling must be taken into account to unveil the intrinsic electronic/magnetic properties of the system.

cond-mat.supr-con↗

arXiv2020

Magnetic structures, spin-flop transition and coupling of Eu and Mn magnetism in the Dirac semimetal EuMnBi$_2$

We report here a comprehensive study of the AFM structures of the Eu and Mn magnetic sublattices as well as the interplay between Eu and Mn magnetism in this compound by using both polarized and non-polarized single-crystal neutron diffraction. Magnetic susceptibility, specific heat capacity measurements and the temperature dependence of magnetic diffractions suggest that the AFM ordering temperature of the Eu and Mn moments is at 22 and 337 K, respectively. The magnetic moments of both Eu and Mn ions are oriented along the crystallographic $c$ axis, and the respective magnetic propagation vector is $\textbf{k}_{Eu} = (0,0,1)$ and $\textbf{k}_{Mn}=(0,0,0)$. With proper neutron absorption correction, the ordered moments are refined at 3 K as 7.7(1) $μ_B$ and 4.1(1) $μ_B$ for the Eu and Mn ions, respectively. In addition, a spin-flop (SF) phase transition of the Eu moments in an applied magnetic field along the $c$ axis was confirmed to take place at a critical field of B$_c$ $\sim$ 5.3 T. The evolution of the Eu magnetic moment direction as a function of the applied magnetic field in the SF phase was also determined. Clear kinks in both field and temperature dependence of the magnetic reflections ($\pm1$, 0, 1) of Mn were observed at the onset of the SF phase transition and the AFM order of the Eu moments, respectively. This unambiguously indicates the existence of a strong coupling between Eu and Mn magnetism. The interplay between two magnetic sublattices could bring new possibilities to tune Dirac fermions via changing magnetic structures by applied fields in this class of magnetic topological semimetals.

cond-mat.str-el↗

arXiv2017

Evolution of the partially frustrated magnetic order in CePd$_{1-x}$Ni$_x$Al

We report on a single-crystal neutron diffraction study of the evolution of the antiferromagnetic order in the heavy-fermion compound CePd$_{1-x}$Ni$_x$Al which exhibits partial geometric frustration due to its distorted Kagomé structure. The magnetic structure is found to be unchanged with a propagation vector $Q_\mathrm{AF} \approx (0.5~0~0.35)$ for all Ni concentrations $x$ up to $x_c \approx 0.14$. Upon approaching the quantum critical concentration $x_c$, the ordered moment vanishes linearly with Néel temperature $T_{\rm N}$, in good agreement with CePdAl under hydrostatic pressure. For all Ni concentrations, substantial short-range magnetic correlations are observed above $T_{\rm N}$ as a result of frustration.

cond-mat.str-el↗

arXiv2015

Distinct itinerant spin-density waves and local-moment antiferromagnetism in an intermetallic ErPd$_2$Si$_2$ single crystal

Identifying the nature of magnetism, itinerant or localized, remains a major challenge in condensed-matter science. Purely localized moments appear only in magnetic insulators, whereas itinerant moments more or less co-exist with localized moments in metallic compounds such as the doped-cuprate or the iron-based superconductors, hampering a thorough understanding of the role of magnetism in phenomena like superconductivity or magnetoresistance. Here we distinguish two antiferromagnetic modulations with respective propagation wave vectors of $Q_{\pm}$ = ($H \pm 0.557(1)$, 0, $L \pm 0.150(1)$) and $Q_\text{C}$ = ($H \pm 0.564(1)$, 0, $L$), where $\left(H, L\right)$ are allowed Miller indices, in an ErPd$_2$Si$_2$ single crystal by neutron scattering and establish their respective temperature- and field-dependent phase diagrams. The modulations can co-exist but also compete depending on temperature or applied field strength. They couple differently with the underlying lattice albeit with associated moments in a common direction. The $Q_{\pm}$ modulation may be attributed to localized 4\emph{f} moments while the $Q_\text{C}$ correlates well with itinerant conduction bands, supported by our transport studies. Hence, ErPd$_2$Si$_2$ represents a new model compound that displays clearly-separated itinerant and localized moments, substantiating early theoretical predictions and providing a unique platform allowing the study of itinerant electron behavior in a localized antiferromagnetic matrix.

cond-mat.str-el↗

arXiv2014

Incommensurate antiferromagnetic order in the manifoldly-frustrated SrTb$_2$O$_4$ with transition temperature up to 4.28 K

The N$\acute{\rm e}$el temperature of the new frustrated family of Sr\emph{RE}$_2$O$_4$ (\emph{RE} = rare earth) compounds is yet limited to $\sim$ 0.9 K, which more or less hampers a complete understanding of the relevant magnetic frustrations and spin interactions. Here we report on a new frustrated member to the family, SrTb$_2$O$_4$ with a record $T_{\rm N}$ = 4.28(2) K, and an experimental study of the magnetic interacting and frustrating mechanisms by polarized and unpolarized neutron scattering. The compound SrTb$_2$O$_4$ displays an incommensurate antiferromagnetic (AFM) order with a transverse wave vector \textbf{Q}$^{\rm 0.5 K}_{\rm AFM}$ = (0.5924(1), 0.0059(1), 0) albeit with partially-ordered moments, 1.92(6) $μ_{\rm B}$ at 0.5 K, stemming from only one of the two inequivalent Tb sites mainly by virtue of their different octahedral distortions. The localized moments are confined to the \emph{bc} plane, 11.9(66)$^\circ$ away from the \emph{b} axis probably by single-ion anisotropy. We reveal that this AFM order is dominated mainly by dipole-dipole interactions and disclose that the octahedral distortion, nearest-neighbour (NN) ferromagnetic (FM) arrangement, different next NN FM and AFM configurations, and in-plane anisotropic spin correlations are vital to the magnetic structure and associated multiple frustrations. The discovery of the thus far highest AFM transition temperature renders SrTb$_2$O$_4$ a new friendly frustrated platform in the family for exploring the nature of magnetic interactions and frustrations.

cond-mat.str-el↗

arXiv2014

Nonmagnetic ordering state of single-crystal SrTm$_2$O$_4$: A polarized and unpolarized neutron-scattering study

Our single-crystal polarized neutron scattering at 65 mK and powder unpolarized neutron diffraction at 0.5 K show no evidence for a long-range magnetic order and even detect no sign of diffuse magnetic neutron scattering in single-crystal SrTm2O4. The data refinements reveal that the two TmO6 octahedral distortion modes are the same as those of the TbO6 octahedra in SrTb2O4, i.e., one distortion is stronger than the other one especially at low temperatures, which is attributed probably to different crystal electric fields for the two inequivalent octahedra. Consequently, we conclude that SrTm2O4 has no magnetic order, neither long-ranged nor short-ranged, even down to 65 mK. Therefore, SrTm2O4 is a different compound from its brethren in the new family of frustrated SrRE2O4 (RE = Gd, Tb, Dy, Ho, Er, and Yb) magnets. We propose that crystal field anisotropy may dominate over weak dipolar spin interactions in SrTm2O4, leading to a virtually nonmagnetic ordering state.

cond-mat.str-el↗

arXiv2011

Cooperative long range protein-protein dynamics in Purple Membrane

We present experimental evidence for a long-range protein-protein interaction in purple membrane (PM). The interprotein dynamics were quantified by measuring the spectrum of the acoustic phonons in the 2D bacteriorhodopsin (BR) protein lattice using inelastic neutron scattering. Phonon energies of about 1 meV were determined. The data are compared to an analytical model, and the effective spring constant for the interaction between neighboring protein trimers are determined to be k=53 N/m. Additional, optical-like excitations at 0.45 meV were found and assigned to intraprotein dynamics between neighboring BR monomers.

physics.bio-ph↗