arXiv subjects

Alannah M. Hallas

Publications and source records attributed to Alannah M. Hallas.

At least 19 recordsLinked to original sources

arXiv2026

Geometric Approach to the High-Throughput Identification of Honeycomb Materials

The honeycomb lattice is an iconic structural motif in condensed matter physics. However, emerging theoretical models require the identification of new honeycomb lattice materials with strict specification on their structural, magnetic, and electronic characteristics. In this work, we introduce a filtering algorithm using simple geometric arguments to detect materials with honeycomb structural motifs. We classify four unique categories of lattices: conventional honeycombs, hyperhoneycombs, staircase or zigzag honeycombs, and fully 3D honeycombs. We also identify several distortion motifs in the conventional honeycomb set: elongated, sheared, and buckled honeycombs. We describe several screening criteria for further analysis of honeycomb systems, specifically the quantification of exfoliability in 2D materials, the identification of magnetic honeycombs, and a density-of-states peak quality metric for identification of electronic instabilities. The database containing the results of the filters and subsequent analysis is a useful tool for identifying novel materials for targeted physical phenomena for experimental characterization.

cond-mat.str-el↗

arXiv2026

Prominent Dimensional Effects on High-order Harmonic Generation in Strongly Correlated Electron Systems

Dimensionality strongly affects elementary excitations in correlated quantum materials, yet its impact on extreme nonlinear optical responses remains largely unexplored. Here, we combine high-harmonic generation (HHG) experiments on quasi-one-dimensional SrCuO$_2$ and quasi-two-dimensional Pr$_2$CuO$_4$ with nonequilibrium simulations of Hubbard models. We find a pronounced dimensional contrast: SrCuO$_2$ exhibits a robust plateau-like high-harmonic spectrum with weak temperature dependence, whereas Pr$_2$CuO$_4$ shows a monotonic decrease in harmonic yield and strong thermal suppression, especially at higher harmonics. The simulations qualitatively reproduce these trends and identify dimensionality-dependent doublon--holon dephasing, governed by spin--charge coupling, as their microscopic origin. These results establish dimensionality and spin--charge coupling as key control parameters for extreme nonlinear optical responses in correlated insulators.

cond-mat.str-el↗

arXiv2026

Rare-earth oxysulfides RE$_2$O$_2$S as model mixed-anion frustrated magnets

The study of low-dimensional and anisotropic magnetism is a promising avenue for the discovery of novel quantum phenomena. Mixed-anion materials, defined by the coordination of metal cations by two or more distinct anionic species, provide an intrinsically anisotropic platform for the tuning of structural, magnetic, and electronic properties. In this work, we report the synthesis and characterization of a family of rare-earth oxysulfide (RE$_2$O$_2$S) antiferromagnets (AFM) possessing a triangular-bilayer slab lattice geometry. Long-range AFM order is observed for the majority of compositions, with several (RE = Ce, Pr, Nd, Sm) having been previously unreported. Although assumed to form stoichiometrically, pair distribution function (PDF) analysis provides evidence for significant, synthesis-dependent interslab structural disorder as RE$_2$O$_{2+x}$S$_{1-x}$, resulting in significant variability in the bulk magnetic response of the Nd member. This work highlights the tunability of frustrated magnetic ground states in rare-earth-based mixed-anion materials, and the importance of thorough structural characterization in the discovery of new mixed-anion magnets.

cond-mat.str-el↗

arXiv2026

Machine Learning Guided Discovery of Corundum High Entropy Oxides

Early thinking in the field of high entropy oxides (HEOs) emphasized their likely abundance, with combinatorial arguments hinting at a myriad of new materials. The experimental reality has proven more challenging: the stability of HEOs cannot be straightforwardly predicted based on ionic radii, lattice geometry, and charge-balancing considerations alone. In this work, we employ machine learning interatomic potentials (MLIPs) to predict the synthesizability of HEOs of the form $A_2$O$_3$ derived from a selection of trivalent cations. From nearly 500 possible compositions, we identify 16 promising candidates for experimental validation with solid-state and combustion synthesis. We discover three new HEOs in the corundum structure, including (Al,Cr,Fe,Rh,Sc)$_2$O$_3$, and one novel cation-ordered phase, (Al,Fe,Ga,Sc)$_2$O$_3$. By far the most common synthesis outcome was a mixture of competing phases, sometimes involving redox reactions. Our results also reveal profound synthesis method dependence for the final product, where qualitatively equivalent outcomes between the two synthesis methods were only observed for 3 of the 16 tested compositions. We conclude that the occurrence rate of HEOs is far rarer than initially believed and that machine learning approaches can effectively guide us to the "needle in the haystack".

cond-mat.mtrl-sci↗

arXiv2026

Disentangling the contributions of individual cations to magnetic order in a spinel high entropy oxide

High entropy oxides (HEOs) can possess long-range ordered magnetic states despite their extreme chemical disorder. Very little is known about how the different chemical constituents in HEOs contribute to the emergence of these magnetic states. In this work, we leverage element-specific magnetometry attained via x-ray magnetic circular dichroism (XMCD) to understand how magnetic order is driven in two ferrimagnetic spinel-structured HEOs with compositions (Cr,Mn,Fe,Co,Ni)$_3$O$_4$ and (Cr,Mn,Fe,Co,Ni)$_{2.4}$Ga$_{0.6}$O$_4$. We find that while the magnetic transition is simultaneous for all chemical species, the rate at which their magnetic moments grow is strongly cation dependent. This behavior is explained by the varying $\textit{3d}$ crystal field level fillings of the magnetic cations, which in turn determine their ability to participate in the different magnetic exchange pathways available in the spinel structure. Dominant $A$-$B$ sublattice exchange enables some species to harden rapidly ($\textit{e.g.}$ tetrahedral Fe$^{3+}$ and octahedral Ni$^{2+}$) while others exhibit a sluggish transition due to frustration from competing interactions ($\textit{e.g.}$ octahedral Fe$^{3+}$ and Cr$^{3+}$). Non-magnetic substitution suppresses these differences, introducing broken magnetic linkages that relieve frustration. Tailoring the magnetism of HEO spinels therefore requires detailed knowledge of both their site selectivities and their exchange pathways.

cond-mat.mtrl-sci↗

arXiv2026

Coherent high-velocity chiral magnons in the metallic altermagnet CrSb

We report the collective magnetism of the metallic altermagnet CrSb. Magnetic susceptibility and polarized neutron diffraction measurements show that CrSb is a perfectly compensated Ising altermagnet below a Néel temperature of $T_N = 733(4)$ K. Inelastic neutron scattering experiments reveal coherent and highly-dispersive antiferromagnetic spin waves with large group velocities of 61(2) km s$^{-1}$ and 58(2) km s$^{-1}$ along the in-plane and out-of-plane directions, respectively. The observed magnon dispersions along high-symmetry directions of the Brillouin zone are well described by a minimal Heisenberg model up to third nearest neighbors of alternating antiferromagnetic and ferromagnetic character, $J_1 = 23(4)$ meV, $J_2 = -5.4(8)$ meV, $J_3 = 5.2(8)$ meV, and an Ising single-ion anisotropy term $D = 0.15(4)$ meV. We observe clear momentum space signatures of chiral spin splitting along the low-symmetry $Γ$-$L$ direction, characteristic of higher-order altermagnetic exchange interactions, the first such observation in a metallic altermagnet. These findings identify CrSb as a singular material: a metallic altermagnet in which coherent spin-split magnons persist well above room temperature, providing a compelling platform for spintronic applications.

cond-mat.mtrl-sci↗

arXiv2026

Direct Fabrication of a Superconducting Two-Dimensional Electron Gas on KTaO3(111) via Mg-Induced Surface Reduction

Two-dimensional electron gases (2DEGs) at the surfaces of KTaO3 have become an exciting platform for exploring strong spin-orbit coupling, Rashba physics, and low-carrier-density superconductivity. Yet, a large fraction of reported KTaO3-based 2DEGs has been realized through chemically complex overlayers that both generate carriers and can obscure the native electronic structure, making spectroscopic access to the underlying 2DEG challenging. Here, we demonstrate a simple and direct method to generate a superconducting 2DEG on KTaO3(111) using Mg-induced surface reduction in molecular-beam epitaxy (MBE). Mg has an extremely low sticking coefficient at elevated temperatures, enabling the formation of an ultrathin (less than 1-2 monolayers) MgO layer that is transparent to soft x-ray photoemission spectroscopy (XPS) and angle-resolved photoemission spectroscopy (ARPES). This allows direct measurement of the surface chemistry and low-energy electronic structure of the pristine reduced surface without the need for a several-nanometer-thick capping layer. XPS shows clear reduction of Ta5+ to lower oxidation states, while ARPES reveals a parabolic Ta 5d conduction band with an approximately 150 meV bandwidth and additional subband features arising from quantum confinement. Transport measurements confirm a superconducting transition below 0.7 K. Together, these results demonstrate a chemically straightforward and controllable pathway for fabricating spectroscopically accessible superconducting 2DEGs on KTaO3(111), and provide a powerful new platform for investigating the mechanisms underlying orientation-dependent superconductivity in KTaO3-based oxide interfaces.

cond-mat.supr-con↗

arXiv2026

K$_2$Co$_2$(TeO$_{3}$)$_{3}$ $\cdot$ 2.5 H$_2$O : A mineral-inspired pseudo-honeycomb cobalt dimer antiferromagnet

In recent years, magnetically-frustrated triangular and honeycomb lattice cobaltates have seen extensive study in the pursuit of a quantum spin liquid (QSL) state in a real material. In this work, we describe the hydroflux synthesis of K$_2$Co$_2$(TeO$_{3}$)$_{3}$ $\cdot$ 2.5 H$_2$O (KCoTOH), a novel zemannite-type antiferromagnet (AFM) possessing structural elements of both triangular dimer and honeycomb structural motifs. Bulk magnetometry and specific heat data support the onset of long-range AFM order below $T_\text{N}$ = 7.6(1) K, with neutron diffraction and muon spin relaxation ($μ$SR) measurements placing the majority of the ordered moment within the pseudo-honeycomb plane. We resolve three unique oscillation frequencies from the zero-field $μ$SR spectra, additionally suggesting a remarkably low level of structural disorder in as-grown KCoTOH crystals. Whereas interactions between dimerized chains of Co$^{2+}$ cations are typically observed to be negligible or ferromagnetic in nature, the largely planar ordering motif observed in KCoTOH is instead stabilized by net antiferromagnetic interactions through bridging tellurite groups. This work highlights the potential of hydroflux synthesis methods in the stabilization of magnetic materials possessing novel and potentially more frustrated lattice geometries.

cond-mat.str-el↗

arXiv2026

Vanishing ordered moment in the frustrated triangular lattice antiferromagnet CuNdO$_2$

We investigate the magnetic ground state of CuNdO$_2$, which is a delafossite with a triangular lattice of magnetic Nd$^{3+}$ ions that are well separated by non-magnetic Cu spacer layers. From inelastic neutron scattering measurements of the crystal electric field, we determine the strong Ising character of the pseudo-spin 1/2 Nd$^{3+}$ moments. Magnetic susceptibility and heat capacity measurements reveal the onset of long-range antiferromagnetic order at $T_N=0.78$ K. While the magnetic transition is definitively observed with muon spin relaxation, accompanied by the formation of a weakly dispersing spin wave excitation, no dipole-ordered moment is detected with neutron diffraction. We show that the apparent absence of a dipolar ordered moment is a consequence of the dominant Ising character of the antiferromagnetically coupled Nd$^{3+}$ moments, which experience extreme frustration on the triangular lattice. Consequently, the frustration in CuNdO$_2$ is relieved through in-plane ordering of the substantially smaller perpendicular component of the Nd$^{3+}$ moments into a 120\textdegree\ structure, with a nearly vanishing ordered moment.

cond-mat.str-el↗

arXiv2025

More is different: How chemical complexity influences stability in high entropy oxides

Tailoring the chemical composition of a high entropy oxide (HEO) is a powerful approach to enhancing desirable material properties. However, the targeted synthesis of HEO materials is often hindered by competing stabilizing and destabilizing factors, which are difficult to predict. This work examines the effects of increased configurational entropy on the phase formation and stability of four notable complex oxide families: perovskite ($AB$O$_3$), pyrochlore ($A_2B_2$O$_7$), Ruddlesden-Popper ($A_2B$O$_4$), and zirconium tungstate ($AB_2$O$_8$). Each of these structures has a tetravalent cation site, which we attempt to substitute with an entropic mixture of four cations, benchmarked by the parallel synthesis of a non-disordered reference compound. While all four target high entropy materials can be expected to form based on ionic radii criteria, only the high entropy perovskite Ba(Ti,Zr,Hf,Sn)O$_3$ is successfully synthesized. In the case of the pyrochlore, an entropy-stabilized defect fluorite is formed instead, while the Ruddlesden-Popper phase co-exists with multiple competing phases. For the tungstate, an unexpected deep eutectic point between the precursors results in melting that precedes the formation of a high entropy phase. Our case studies therefore illustrate that the stability of HEOs cannot be straightforwardly predicted based on ionic radii, lattice geometry, and charge-balancing considerations alone due to the underlying complexity of the interactions between the many chemical constituents.

cond-mat.mtrl-sci↗

arXiv2025

Intrinsic defect intolerance in the ultra-pure metal PtSn$_4$

Ultra-pure materials are highly valued as model systems for the study of intrinsic physics. Frequently, however, the crystal growth of such pristine samples requires significant optimization. PtSn$_4$ is a rare example of a material that naturally forms with a very low concentration of crystalline defects. Here, we investigate the origin of its low defect levels using a combination of electrical resistivity measurements, computational modeling, and scanning tunneling microscopy imaging. While typical flux-grown crystals of PtSn$_4$ can have residual resistivity ratios (RRRs) that exceed 1000, we show that even at the most extreme formation speeds, the RRR cannot be suppressed below 100. This aversion to defect formation extends to both the Pt and Sn sublattices, which contribute with equal weight to the conduction properties. Direct local imaging with scanning tunneling microscopy further substantiates the rarity of point defects, while the prohibitive energetic cost of forming a defect is demonstrated through density functional theory calculations. Taken together, our results establish PtSn$_4$ as an intrinsically defect-intolerant material, making it an ideal platform to study other properties of interest, including extreme magnetoresistance and topology.

cond-mat.mtrl-sci↗

arXiv2025

Expanding the search space of high entropy oxides and predicting synthesizability using machine learning interatomic potentials

We propose an efficient computational methodology for predicting the synthesizability of high entropy oxides (HEOs) in a large space of possible candidate compounds. HEOs are a growing field with an enormous potential chemical composition space, and yet the discovery of new HEOs is slow and driven by experimental trial-and-error. In this work, we attempt to speed up this process by using a machine learned interatomic potential offering DFT-level accuracy. Our methodology starts by identifying a set of crystal structures and elements for screening, building a large random unit cell of each composition and structure, then relaxing this structure. The most promising candidates are distinguished based on the variance of the individual cation energies, which we introduce as our entropy descriptor, and the enthalpy of mixing, which is used as the enthalpy descriptor. The approach is applied to tetravalent HEOs, and its validity is confirmed by comparison to alternative descriptors and DFT calculations for a set of 7 elements. The search is then extended to a set of 14 elements and three crystal structures, where it successfully identifies the only known stable 4-component HEO in the $α$-PbO$_2$ structure, as well as predicting several new 5-component candidate systems. This approach can straightforwardly be applied to new sets of elements and structures, allowing for the accelerated discovery of new HEOs.

cond-mat.mtrl-sci↗

arXiv2025

Kramers nodal lines in intercalated TaS$_2$ superconductors

Kramers degeneracy is one fundamental embodiment of the quantum mechanical nature of particles with half-integer spin under time reversal symmetry. Under the chiral and noncentrosymmetric achiral crystalline symmetries, Kramers degeneracy emerges respectively as topological quasiparticles of Weyl fermions and Kramers nodal lines (KNLs), anchoring the Berry phase-related physics of electrons. However, an experimental demonstration for ideal KNLs well isolated at the Fermi level is lacking. Here, we establish a class of noncentrosymmetric achiral intercalated transition metal dichalcogenide superconductors with large Ising-type spin-orbit coupling, represented by In$_x$TaS$_2$, to host an ideal KNL phase. We provide evidence from angle-resolved photoemission spectroscopy with spin resolution, angle-dependent quantum oscillation measurements, and ab-initio calculations. Our work not only provides a realistic platform for realizing and tuning KNLs in layered materials, but also paves the way for exploring the interplay between KNLs and superconductivity, as well as applications pertaining to spintronics, valleytronics, and nonlinear transport.

cond-mat.supr-con↗

arXiv2025

The origin and scarcity of breathing pyrochlore lattices in spinel oxides

Breathing pyrochlores are a unique class of materials characterized by a three-dimensional lattice of corner-sharing tetrahedra. However, unlike conventional pyrochlores where all tetrahedra are identical in size, the breathing pyrochlore lattice is composed of alternating large and small tetrahedra. Experimental realizations of the breathing pyrochlore lattice are rare but they do occur in $A$-site ordered spinels, as in the prototype materials LiGaCr$_4$O$_8$ and LiInCr$_4$O$_8$. In this work, we demonstrate that Cr cannot be straightforwardly substituted with other magnetic transition metals while retaining the breathing pyrochlore structure. To explain this observation, we perform density functional theory (DFT) calculations to investigate the formation and stability of LiGaCr$_4$O$_8$ and LiInCr$_4$O$_8$, focusing on the energy scales associated with $A$ and $B$-site orderings as well as the magnetic exchange interactions of Cr ions. We identify the strong octahedral site preference of Cr$^{3+}$ as a key factor in protecting the structural integrity of the pyrochlore sublattice, which in turn enables the breathing distortion to proceed. We also demonstrate that the charge order between the $A$ (Li) and $A'$ sites (Ga or In) is maintained at all temperatures up to decomposition. Furthermore, while the magnetic exchange interactions constitute a relatively small energy scale and therefore do not play a fundamental role in the structural stability of LiGaCr$_4$O$_8$ and LiInCr$_4$O$_8$, magnetism may play a critical role in setting the magnitude of the tetrahedral distortion. Ultimately, we conclude that the scarcity of breathing pyrochlores is a consequence of the stringent requirement on site ordering for their formation.

cond-mat.mtrl-sci↗

arXiv2024

Impact of synthesis method on the structure and function of high entropy oxides

The term sample dependence describes the troublesome tendency of nominally equivalent samples to exhibit different physical properties. High entropy oxides (HEOs) are a class of materials where sample dependence has the potential to be particularly profound due to their inherent chemical complexity. In this work, we prepare a spinel HEO of identical nominal composition by five distinct methods, spanning a range of thermodynamic and kinetic conditions: solid state, high pressure, hydrothermal, molten salt, and combustion syntheses. By structurally characterizing these five samples across all length scales with a variety of x-ray methods, we find that while the average structure is unaltered, the samples vary significantly in their local structures and their microstructures. The most profound differences are observed at intermediate length scales, both in terms of crystallite morphology and cation homogeneity. As revealed by x-ray fluorescence microscopy ideal cation homogeneity is achieved only in the case of combustion synthesis. These structural differences in turn significantly alter the observed functional properties, which we demonstrate via characterization of their magnetic response. While ferrimagnetic order is retained across all five samples, the sharpness of the transition, the size of the saturated moment, and the coercivity all show marked variations with synthesis method. We conclude that the chemical flexibility inherent to HEOs is complemented by strong synthesis method dependence, providing another axis along which to optimize these materials for a wide range of applications.

cond-mat.mtrl-sci↗

arXiv2024

Tetragonal BaCoO$_3$: A Co$^{4+}$ Ferromagnetic Mott Insulator with Inverted Spin Crossover

The interplay between crystal electric field splitting of d states and Hund's rule exchange energy in cobalt-based perovskites offers a promising avenue for inducing spin-state transitions. This study reports a new body-centered tetragonal (BCT) phase of BaCoO$_3$ (BCT-BaCoO$_3$), synthesized under high pressure (15 GPa) and high temperature (1200 °C) conditions. BCT-BaCoO$_3$ adopts a double perovskite structure of EuTiO$_3$-type (space group I4/mcm, #140), confirmed by high-resolution scanning transmission electron microscopy. X-ray photoelectron spectroscopy reveals a rare Co$^{4+}$ valence state. Magnetization and X-ray absorption measurements reveal a low-spin to high-spin transition that takes place between 200 and 300 K. While spin crossovers are relatively common among common oxides, the one observed in BCT-BaCoO$_3$ is remarkable in that it proceeds in the opposite direction from conventional spin transitions. BCT-BaCoO$_3$ exhibits a low-spin (S = 1/2) state at high temperatures and transitions to a high-spin (S = 5/2) state at low temperatures. Within the high-spin state, hard ferromagnetic order onsets at T$_C$ = 107 K. Electrical resistivity indicates weak magnetoresistance and insulating behavior. Overall, BCT-BaCoO$_3$ presents an exceptional model for the exploration of spin-state transitions and the study of Co spin states in cobalt-based perovskites.

cond-mat.mtrl-sci↗

arXiv2024

Short-range order and local distortions in entropy stabilized oxides

An idealized high entropy oxide is characterized by perfect chemical disorder and perfect positional order. In this work, we investigate the extent to which short-range order (SRO) and local structural distortions impede that idealized scenario. Working in the entropy stabilized $α$-PbO$_2$ structure, we compare a two-component system, (Ti,Zr)O$_2$, with a four-component system, (Ti,Zr,Hf,Sn)O$_2$, using a combination of experimental and computational approaches. Special quasi-random structures are used in conjunction with density functional theory calculations to investigate the local distortions around specific elements revealing significant local distortions that are relatively insensitive to the number of chemical constituents. Using finite temperature Monte Carlo simulations, we are able to reproduce the previously experimentally observed SRO and transition temperature for the two-component system. However, the ideal configurational entropy is never reached, so SRO is expected even at synthesis temperatures. On the other hand, the order-disorder transition temperature is dramatically lower and experimentally inaccessible for the four-component system, while the configurational entropy is closer to ideal and less sensitive to temperature. Total scattering measurements and pair distribution function analysis of slow-cooled and quenched samples support this view. In general, we demonstrate that SRO effects in high entropy materials are less prevalent as more components are added in, provided the pairwise interaction strengths remain comparable, while local distortions are less affected by the number of components.

cond-mat.mtrl-sci↗

arXiv2024

Effect of high pressure synthesis conditions on the formation of high entropy oxides

High entropy materials are often entropy stabilized, meaning that the configurational entropy from multiple elements sharing a single lattice site stabilizes the structure. In this work, we study how high-pressure synthesis conditions can stabilize or destabilize a high entropy oxide (HEO). We study the high-pressure and high-temperature phase equilibria of two well-known families of HEOs: the rock-salt structured compound (Mg,Co,Ni,Cu,Zn)O including some cation substitutions and the spinel structured (Cr,Mn,Fe,Co,Ni)$_3$O$_4$. Syntheses were performed at various temperatures, pressures, and oxygen activity levels resulting in dramatically different synthesis outcomes. In particular, in the rock salt HEO we observe the competing tenorite and wurtzite phases and the possible formation of a layered rock salt phase, while the spinel HEO is highly susceptible to decomposition into a mixture of rock-salt and corundum phases. At the highest tested pressures, 15 GPa, we discover the transformation of the spinel HEO into a metastable modified ludwigite-type structure with nominal formula (Cr,Mn,Fe,Co,Ni)$_4$O$_5$. The relationship between the synthesis conditions and the final reaction product is not straightforward. Nonetheless, we conclude that high-pressure conditions provide an important opportunity to synthesize high entropy phases that cannot be formed any other way.

cond-mat.mtrl-sci↗