arXiv subjects

C. Ritter

Publications and source records attributed to C. Ritter.

At least 19 recordsLinked to original sources

arXiv2026

Hidden Magnetic Octupolar Order driven by Spin-Orbit coupling in KFeF$_3$

Phase transitions are typically driven by symmetry-breaking structural distortions that lift electronic degeneracies, yet in some cases, these transitions may be driven by a hidden order without conventional structural signatures. Here, we demonstrate that the 3$d$ perovskite, KFeF$_3$, hosts such a hidden instability. Using a combination of high-resolution powder diffraction, magnetometry, symmetry-based analysis and first principles calculations, we reveal that while the 90 K cubic to rhombohedral transition arises from conventional magnetostriction accompanying antiferromagnetic order, a second transition at 40 K lowers the symmetry to monoclinic without any detectable Jahn-Teller distortion or translational symmetry-breaking. Symmetry-based Landau analysis supports a hidden zone centered magnetic octupole order parameter, whose improper coupling accounts for the weak ferromagnetism and pronounced symmetry-breaking strain. Density functional calculations show that spin-orbit coupling suppresses the competing Jahn-Teller instability, and thereby favors higher rank magnetic multipolar degrees of freedom. These findings establish KFeF$_3$ as a model system in which the competing energy scales between spin-orbit coupling and orbital degeneracy result in the emergence of hidden, multipolar order. We show that the control of such magnetic, multipolar order could, in principle, provide a route to induce altermagnetism.

cond-mat.str-el↗

arXiv2026

Unveiling the magnetic ground states in the iridate double perovskite Pr(2-x)SrxMgIrO6 (x = 0 and 0.5) series

We report here the results of a detailed magnetic, thermodynamic, and neutron powder diffraction (NPD) studies carried out on the double perovskite iridates Pr(2-x)SrxMgIrO6 (x = 0 and 0.5). Temperature dependent bulk DC susceptibility data clearly reveals a sharp antiferromagnetic (AFM) transition at 14.5 K in Pr2MgIrO6(x = 0). Next, a weaker signature of an AFM transition at a lower temperature (6 K) is observed in x = 0.5 i.e., Pr1.5Sr0.5MgIrO6 (PSMIO1505). The observed magnetic transitions are further corroborated by the presence of anomalies around the same temperatures in our T-dependent specific heat results. The charge states of both Pr and Ir cations have been confirmed to be the expected ones (3+ for Pr in both the compounds, while Ir is in a pure 4+ state for x = 0 and in a mixed 4+/5+ state for x = 0.5) from the core-level x-ray photoemission spectroscopy (XPS) measurements. Using neutron powder diffraction (NPD) the magnetic ground states and the magnetic moment values were determined for both compounds. Both the Pr- and Ir-sites undergo AFM ordering below the respective transition temperatures, designated by the propagation vector k = ( 1/2 , 0, 1/2 ), in both the compounds.

cond-mat.str-el↗

arXiv2026

Microscopic origin of hard-plane antiferromagnetism in the Kondo lattice Ce2Rh3Ge5

Hard plane antiferromagnetic order where ordered moments lie perpendicular to the single-ion crystal electric field easy axis is rare in Ce-based Kondo lattices and is a subject of active interest. Here we show that Ce$_2$Rh$_3$Ge$_5$ realizes a hard-plane antiferromagnetic state in which partial delocalization of the local moment gives rise to an RKKY exchange that overturns the single-ion easy-axis preference. Neutron diffraction reveals moments in the $ab$ plane, while inelastic neutron scattering and susceptibility establish a magnetic easy axis along $c$ in the paramagnetic regime, highlighting a clear inversion between single-ion and ordered-state anisotropies. In this work, we establish a unified microscopic framework to consistently account for partial $4f$-moment delocalization, enhanced in-plane RKKY exchange, and the resulting hard-plane antiferromagnetic order. Ce$_2$Rh$_3$Ge$_5$ thus provides a benchmark system in which single-ion anisotropy, Kondo screening, and RKKY exchange compete on comparable energy scales, revealing a cooperative route to hard-axis ordering in strongly hybridized Kondo lattices.

cond-mat.str-el↗

arXiv2025

Signatures of Orbital Order and Disorder in Fluoro-Perovskites with $t_{2g}$ Electronic Degeneracies

A detailed high-resolution, variable temperature powder diffraction study of the fluoro-perovskites NaFeF$_3$ and NaCoF$_3$ is performed to probe their orbital ordering transitions. Through analysis of the symmetry adapted macrostrains and atomic distortions, we show that NaFeF$_3$ undergoes a C-type orbital order transition associated with the $t_{2g}^4$ states of Fe$^{2+}$. Counter-intuitively, the phase transition leading to the orbital order appears second order-like, which contradicts the thermodynamic requirements for electronic and isosymmeric phase transitions, implying that there must be an associated hidden symmetry breaking. On the other hand, for NaCoF$_3$, consideration of the symmetry adapted strains allows us to confidently rule out the occurrence of any long-range orbital orders down to 4 K. Since NaCoF$_3$ is an insulator with quenched orbital angular momentum at this temperature, our findings point towards a novel kind of orbital disorder associated to the $t_{2g}^5$ electronic degeneracy.

cond-mat.str-el↗

arXiv2025

Goldstone-mediated polar instability in hexagonal barium titanate

We discover a rare structural manifestation of the Goldstone paradigm in a hexagonal polytype of the archetypal ferroelectric BaTiO3. First-principles calculations confirm the Goldstone character of the order parameter, and high-resolution diffraction measurements link this to a quasi-continuous domain texture in the vicinity of the low-temperature phase transitions. Our findings highlight how changes in structural topology may be exploited to realize rich polar topologies in bulk ferroelectric perovskites.

cond-mat.mtrl-sci↗

arXiv2025

Quasi-two-dimensional magnetism and antiferromagnetic ground state in Li$_2$FeSiO$_4$

Our experimental (neutron diffraction, M\"ossbauer spectroscopy, magnetic susceptibility, specific heat) and numerical studies on the evolution of short- and long-range magnetic order in $\gamma_{\rm II}$-Li$_2$FeSiO$_4$ suggest a quasi-two-dimensional (2D) nature of magnetism. The experimental data obtained on single crystals imply long-range antiferromagnetic order below $T_{\rm N}= 17$~K. A broad maximum in magnetic susceptibility $\chi$ at $T_{\rm m}\simeq 28$~K, observation of magnetic entropy changes up to 100~K and anisotropy in $\chi$ are indicative of low-dimensional magnetism and suggest short-range magnetic correlations up to 200~K. Neutron diffraction shows that long-range antiferromagnetic order is characterised by the propagation vector k=(1/2,0,1/2). The ordered moment $\mu = 2.50(2) \mu_B$ /Fe, at $T = 1.5$~K, is along the crystallographic $a$-axis. This is consistent with the observed static hyperfine field of $B_{\rm hyp}=14.8(3)$\,T by M\"ossbauer spectroscopy which indicates significant orbital contributions. The temperature dependence of $B_{\rm hyp}$ yields the critical exponent $\beta=0.116(12)$ which is in the regime of the 2D Ising behaviour. LSDA+U studies exploiting the experimental spin structure suggest dominating magnetic exchange coupling within the $ac$-layers (i.e., $J_3\simeq -6$~K and $J_6\simeq-2$~K) while interlayer coupling is much smaller and partly frustrated. This confirms the 2D nature of magnetism and is in full agreement with the experimental findings.

cond-mat.str-el↗

arXiv2024

Magnetic structure and crystal field states of antiferromagnetic CeNiGe$_3$: Neutron scattering and $\mu$SR investigations

We present the results of microscopic investigations of antiferromagnetic CeNiGe$_3$, using neutron powder diffraction (NPD), inelastic neutron scattering (INS), and muon spin relaxation ($\mu$SR) measurements. CeNiGe$_3$ crystallizes in a centrosymmetric orthorhombic crystal structure (space group: $Cmmm$) and undergoes antiferromagnetic (AFM) ordering. The occurrence of long-range AFM ordering at $T_{\rm N} \approx 5.2$~K is confirmed by magnetic susceptibility, heat capacity, neutron diffraction, and $\mu$SR measurements. The NPD data characterize the AFM state with an incommensurate helical magnetic structure having a propagation vector $k$ = (0, 0.41, 1/2). In addition, INS measurements at 10~K identified two crystal electric field (CEF) excitations at 9.17~meV and 18.42~meV. We analyzed the INS data using a CEF model for an orthorhombic environment of Ce$^{3+}$ ($J=5/2$) and determined the CEF parameters and ground state wavefunctions of CeNiGe$_3$. Moreover, zero-field $\mu$SR data for CeNiGe$_3$ at $T< T_{\rm N}$ show long-range AFM ordering with three distinct oscillation frequencies corresponding to three different internal fields at the muon sites. The internal fields at the muon-stopping sites have been further investigated using density functional theory calculations.

cond-mat.str-el↗

arXiv2024

Growth of Ba_2CoWO_6 Single Crystals and their Magnetic, Thermodynamic and Electronic Properties

This study explores the bulk crystal growth, structural characterization, and physical property measurements of the cubic double perovskite Ba_2CoWO_6(BCWO). In BCWO, Co+2 ions form a face-centered cubic (FCC) lattice with non-distorted cobalt octahedra. The compound exhibits long-range antiferromagnetic order below TN = 14 K. Magnetization data indicated a slight anisotropy along with a spin-flop transition at 10 kOe , a saturation field of 310 kOe and an ordered moment of 2.17 Mu_B at T = 1.6 K. Heat capacity measurements indicate an effective j = 1/2 ground state configuration, resulting from the combined effects of the crystal electric field and spin-orbit interaction. Surface photovoltage analysis reveals two optical gaps in the UV-Visible region, suggesting potential applications in photocatalysis and photovoltaics. The magnetic and optical properties highlight the significant role of orbital contributions within BCWO, indicating various other potential applications.

cond-mat.str-el↗

arXiv2024

High-entropy magnetism of murunskite

Murunskite (K$_2$FeCu$_3$S$_4$) is a bridging compound between the only two known families of high-temperature superconductors. It is a semiconductor like the parent compounds of cuprates, yet isostructural to metallic iron-pnictides. Moreover, like both families, it has an antiferromagnetic (AF)-like response with an ordered phase occurring below $\approx$ 100 K. Through comprehensive neutron, M\"ossbauer, and XPS measurements on single crystals, we unveil AF with a nearly commensurate quarter-zone wave vector. Intriguingly, the only identifiable magnetic atoms, iron, are randomly distributed over one-quarter of available crystallographic sites in 2D planes, while the remaining sites are occupied by closed-shell copper. Notably, any interpretation in terms of a spin-density wave is challenging, in contrast to the metallic iron-pnictides where Fermi-surface nesting can occur. Our findings align with a disordered-alloy picture featuring magnetic interactions up to second neighbors. Moreover, in the paramagnetic state, iron ions are either in Fe$^{3+}$ or Fe$^{2+}$ oxidation states, associated with two distinct paramagnetic sites identified by M\"ossbauer spectroscopy. Upon decreasing the temperature below the appearance of magnetic interactions, these two signals merge completely into a third, implying an orbital transition. It completes the cascade of (local) transitions that transform iron atoms from fully orbitally and magnetically disordered to homogeneously ordered in inverse space, but still randomly distributed in real space.

cond-mat.str-el↗

arXiv2023

Experimental Evidence for the Spiral Spin Liquid in LiYbO$_2$

Spiral spin liquids are an exotic class of correlated paramagnets with an enigmatic magnetic ground state composed of a degenerate manifold of fluctuating spin spirals. Experimental realisations of the spiral spin liquid are scarce, mainly due to the prominence of structural distortions in candidate materials that can trigger order-by-disorder transitions to more conventionally ordered magnetic ground states. Expanding the pool of candidate materials that may host a spiral spin liquid is therefore crucial to realising this novel magnetic ground state and understanding its robustness against perturbations that arise in real materials. Here, we show that the material LiYbO$_2$ is the first experimental realisation of a spiral spin liquid predicted to emerge from the $J_1$-$J_2$ Heisenberg model on an elongated diamond lattice. Through a complementary combination of high-resolution and diffuse neutron magnetic scattering studies on a polycrystalline sample, we demonstrate that LiYbO$_2$ fulfils the requirements for the experimental realisation of the spiral spin liquid and reconstruct single-crystal diffuse neutron magnetic scattering maps that reveal continuous spiral spin contours -- a characteristic experimental hallmark of this exotic magnetic phase.

cond-mat.str-el↗

arXiv2022

Magnetically ordered and kagome quantum spin liquid states in the Zn-doped claringbullite series

Neutron scattering measurements have been performed on deuterated powder samples of claringbullite and Zn-doped claringbullite (Zn$_x$Cu$_{4-x}$(OD)$_{6}$FCl). At low temperatures, claringbullite Cu$_4$(OD)$_{6}$FCl forms a distorted pyrochlore lattice with long-range magnetic order and spin-wave-like magnetic excitations. Partial Zn doping leads to the nominal ZnCu$_3$(OD)$_{6}$FCl compound, a geometrically frustrated spin-1/2 kagome antiferromagnet that shows no transition to magnetic order down to 1.5 K. The magnetic excitations form a gapless continuum, a signature of fractional excitations in a quantum spin liquid.

cond-mat.str-el↗

arXiv2022

Quantum critical spin-liquid-like behavior in S = 1/2 quasikagome lattice CeRh1-xPdxSn investigated using muon spin relaxation and neutron scattering

We present the results of muon spin relaxation ($\mu$SR) and neutron scattering on the Ce-based quasikagome lattice CeRh$_{1-x}$Pd$_{x}$Sn ($x=0.1$ to 0.75). Our ZF-$\mu$SR results reveal the absence of static long-range magnetic order down to 0.05~K in $x = 0.1$ single crystals. The weak temperature-dependent plateaus of the dynamic spin fluctuations below 0.2~K in ZF-$\mu$SR together with its longitudinal-field (LF) dependence between 0 and 3~kG indicate the presence of dynamic spin fluctuations persisting even at $T$ = 0.05~K without static magnetic order. On the other hand, $C_{\text{4f}}$/$T$ increases as --log $T$ on cooling below 0.9~K, passes through a broad maximum at 0.13~K and slightly decreases on further cooling. The ac-susceptibility also exhibits a frequency independent broad peak at 0.16~K, which is prominent with an applied field $H$ along $c$-direction. We, therefore, argue that such a behavior for $x=0.1$ (namely, a plateau in spin relaxation rate ($\lambda$) below 0.2~K and a linear $T$ dependence in $C_{\text{4f}}$ below 0.13~K) can be attributed to a metallic spin-liquid (SL) ground state near the quantum critical point in the frustrated Kondo lattice. The LF-$\mu$SR study suggests that the out of kagome plane spin fluctuations are responsible for the SL behavior. Low energy inelastic neutron scattering (INS) of $x$ = 0.1 reveals gapless magnetic excitations, which are also supported by the behavior of $C_{\text{4f}}$ proportional to $T^{1.1}$ down to 0.06~K.

cond-mat.str-el↗

arXiv2022

Neutron diffraction in MnSb2O6: Magnetic and structural domains in a helicoidal polar magnet with coupled chiralities

MnSb$_{2}$O$_{6}$ is based on the structural chiral $P$321 space group #150 where the magnetic Mn$^{2+}$ moments ($S=5/2$, $L\approx 0$) order antiferromagnetically at $T_\mathrm{N}=12$ K. Unlike the related iron based langasite (Ba$_3$NbFe$_3$Si$_2$O$_{14}$) where the low temperature magnetism is based on a proper helix characterized by a time-even pseudoscalar `magnetic' chirality, the Mn$^{2+}$ ions in MnSb$_{2}$O$_{6}$ order with a cycloidal structure at low temperatures, described instead by a time-even vector `magnetic' polarity. A tilted cycloidal structure has been found [M. Kinoshita et al. Phys. Rev. Lett. 117, 047201 (2016)] to facilitate ferroelectric switching under an applied magnetic field. In this work, we apply polarized and unpolarized neutron diffraction analyzing the magnetic and nuclear structures in MnSb$_{2}$O$_{6}$ with the aim of understanding this magnetoelectric coupling. We find no evidence for a helicoidal magnetic structure with one of the spin envelope axes tilted away from the cycloidal $c$-axis. However, on application of a magnetic field $\parallel$ $\vec{c}$ the spin rotation plane can be tilted, giving rise to a cycloid-helix admixture that evolves towards a distorted helix (zero cycloidal component) for fields great than $\approx$ 2 T. We propose a mechanism for the previously reported ferroelectric switching based on coupled structural and magnetic chiralities requiring only an imbalance of structural chiral domains.

cond-mat.str-el↗

arXiv2022

Magnetic structures of geometrically frustrated SrGd$_2$O$_4$ derived from powder and single-crystal neutron diffraction

We present the low-temperature magnetic structures of SrGd$_2$O$_4$ combining neutron diffraction methods on polycrystalline and single-crystal samples containing the $^{160}$Gd isotope. In contrast to other members of the Sr$Ln_2$O$_4$ family ($Ln$ = lanthanide) this system reveals two long-range ordered magnetic phases, which our diffraction data unambiguously identify. Below $T_{\rm N1}$ = 2.73~K, a $\mathbf{q}_1$ = (0 0 0) magnetic structure is stabilized where ferromagnetic chains along the $c$~axis (space group $Pnam$) are coupled antiferromagnetically with neighboring chains. On cooling below $T_{\rm N2}$ = 0.48~K, an additional incommensurate component modulated by $\mathbf{q}_2$ = (0~0~0.42) evolves and aligned along either of the perpendicular axes for the two different Gd sites, resulting in a fan-like magnetic structure. The identification of the particular Gd sites with the magnetic order observed with neutron diffraction is facilitated by a detailed analysis of the crystal fields acting on the sites. The observed ordering phenomena underline the complex multiaxial anisotropy in this system.

cond-mat.str-el↗

arXiv2021

Crystal Electic Field and Possible Coupling with Phonon in Kondo lattice CeCuGa3

We investigate the magnetic and crystal electric field (CEF) states of the Kondo lattice system CeCuGa3 by muon spin relaxation (muSR), neutron diffraction, and inelastic neutron scattering (INS) measurements. A noncentrosymmetric BaNiSn3-type tetragonal crystal structure (space group I4mm) is inferred from x-ray as well as from neutron powder diffraction. The low-temperature magnetic susceptibility and heat capacity data show an anomaly near 2.3 - 2.5~K associated with long range magnetic ordering, which is further confirmed by muSR and neutron diffraction data. The neutron powder diffraction collected at 1.7 K shows the presence of magnetic Bragg peaks indexed by an incommensurate magnetic propagation vector k = (0.148, 0.148, 0) and the magnetic structure is best described by a longitudinal spin density wave with ordered moments lying in ab-plane. An analysis of the INS data based on a CEF model reveals the presence of two magnetic excitations near 4.5 meV and 6.9 meV. The magnetic heat capacity data suggest an overall CEF splitting of 20.7 meV, however the excitation between 20 and 30 meV is very broad and weak in our INS data, but could provide an evidence of CEF level in this energy range in agreement with the magnetic entropy. Our analysis of INS data based on the CEF-phonon model indicates that the two excitations at 4.5 meV and 6.9 meV have their origin in CEF-phonon coupling (i.e. splitting of one CEF peak into two peaks, called vibron), with an overall splitting of 28.16 meV, similar to the case of CeCuAl3 and CeAuAl3.

cond-mat.str-el↗

arXiv2021

Investigation of the magnetic ground state of GaV$_4$S$_8$ using powder neutron diffraction

The magnetic ground state of polycrystalline N\'eel skyrmion hosting material GaV$_4$S$_8$ has been investigated using ac susceptibility and powder neutron diffraction. In the absence of an applied magnetic field GaV$_4$S$_8$ undergoes a transition from a paramagnetic to a cycloidal state below 13~K and then to a ferromagnetic-like state below 6~K. With evidence from ac susceptibility and powder neutron diffraction, we have identified the commensurate magnetic structure at 1.5 K, with ordered magnetic moments of $0.23(2)~\mu_{\mathrm{B}}$ on the V1 sites and $0.22(1)~\mu_{\mathrm{B}}$ on the V2 sites. These moments have ferromagnetic-like alignment but with a 39(8)$^{\circ}$ canting of the magnetic moments on the V2 sites away from the V$_4$ cluster. In the incommensurate magnetic phase that exists between 6 and 13 K, we provide a thorough and careful analysis of the cycloidal magnetic structure exhibited by this material using powder neutron diffraction.

cond-mat.str-el↗

arXiv2021

Magnetic structure and low temperature properties of geometrically frustrated SrNd$_2$O$_4$

We report the low-temperature properties of SrNd$_2$O$_4$, a geometrically frustrated magnet. Magnetisation and heat capacity measurements performed on polycrystalline samples indicate the appearance of a magnetically ordered state at $T_{\rm N}=2.28(4)$~K. Powder neutron diffraction measurements reveal that an \afm\ state with the propagation vector \QV\ is stabilised below this temperature. The magnetic order is incomplete, as only one of the two Nd$^{3+}$ sites carries a significant magnetic moment while the other site remains largely disordered. The presence of a disordered magnetic component below $T_{\rm N}$ is confirmed with polarised neutron diffraction measurements. In an applied magnetic field, the bulk properties measurements indicate a phase transition at about 30~kOe. We construct a tentative $H$-$T$ phase diagram of \sno\ from these measurements.

cond-mat.str-el↗

arXiv2021

Distinct magnetic ground states of $R_2$ZnIrO$_6$ ($R$ = La and Nd) determined by neutron powder diffraction

Double perovskite iridates $A_2$ZnIrO$_6$ ($A$ = alkaline or lanthanide) show complex magnetic behaviors ranging from weak ferromagnetism to successive antiferromagnetic transitions. Here we report the static ($dc$) and dynamic ($ac$) magnetic susceptibility, and neutron powder diffraction measurements for $A$ = La and Nd compounds to elucidate the magnetic ground state. Below 10~K, the $A$ = La compound is best described as canted iridium moments in an antiferromagnet arrangement with a propagation vector \textbf{k} = 0 and a net ferromagnetic component along the $c$-axis. On the other hand, Nd$_2$ZnIrO$_6$ is described well as an antiferromagnet with a propagation vector \textbf{k} = (1/2~1/2~0) below $T_\mathrm{N} \sim$ 17 K. Scattering from both the Nd and Ir magnetic sublattices were required to describe the data and both were found to lie almost completely within the $ab$-plane. $Dc$ susceptibility revealed a bifurcation between the zero-field-cooled and field-cooled curves below $\sim$13 K in Nd$_2$ZnIrO$_6$. A glassy state was ruled out by $ac$ susceptibility but detailed magnetic isotherms revealed the opening of the loop below 13~K. These results suggest a delicate balance exists between the Dzyaloshinskii-Moriya, crystal field schemes, and $d$-$f$ interaction in this series of compounds.

cond-mat.str-el↗