arXiv subjects

Dominik Daisenberger

Publications and source records attributed to Dominik Daisenberger.

13 recordsLinked to original sources

arXiv2026

Comparative high-pressure study on rare-earth entropy fluorite-type oxides

We report a comparative high-pressure study of two fluorite-type rare-earth oxides with increasing configurational entropy, (CePr)O$_{2-δ}$ and (CePrLa)O$_{2-δ}$. Synchrotron-based powder X-ray diffraction and Raman spectroscopy were carried out up to 30 GPa and 20 GPa, respectively. Both compounds retain the cubic fluorite structure throughout the pressure range explored, although an anomaly is observed between 9-16 GPa, characterized by a compressibility plateau and changes in vibrational modes. This behavior is attributed to local lattice distortions and a progressive bond angle bending rather than abrupt phase transitions. In (CePrLa)O$_{2-δ}$, the onset of amorphization is observed above 22 GPa, highlighting its reduced structural stability. The bulk modulus of both systems shows a slight decrease after the onset of the anomaly, suggesting subtle lattice softening. Raman spectroscopy reveals suppression of the F$_{2g}$ mode intensity with increasing cationic disorder, and under compression, partial reordering is evidenced by an increase in the RE-O mode intensity. Our results highlight the complex interplay between configurational entropy, cation size, and pressure in determining the structural stability and vibrational properties of rare-earth high-entropy oxides and provide insight into the mechanisms governing their resilience and local disorder under extreme conditions.

cond-mat.mtrl-sci↗

arXiv2026

Emergent Polar Metal Phase in a Van der Waals Mott Magnet

We report the emergence of a two-dimensional (2D) polar metal phase in van der Waals compound FePSe$_3$ under moderate pressures. This layered material is a Mott insulator with antiferromagnetic order under ambient conditions. We show that FePSe$_3$ uniquely allows tuning a 2D correlated insulator into an exotic metal state where a loss of inversion symmetry leads to periodic polar displacements of ions, within a conducting phase - a polar metal. Our combined synchrotron and neutron diffraction data allow us to present a long-sought, unambiguous high-pressure structural model and show the polar displacements of this new phase. We also observe the suppression of magnetic ordering at the insulator-to-metal transition correspondent with this structural change. Our work outlines a comprehensive temperature-pressure phase diagram of FePSe$_3$, combining detailed structural, magnetic and transport data. The high-pressure phase exhibits activated semiconductor behavior at high temperatures, a $T^2$-dependence in its resistivity at lower temperatures - despite the conditions required for a `good metal' Fermi-Liquid description not being met in this case - and a low-temperature resistivity upturn which is suppressed as the system is tuned away from the concomitant transitions. The realisation of a tunable 2D polar metal state in FePSe$_3$ due to the loss of its inversion symmetry combined with pressure-induced metallicity offers a promising new platform to investigate this exotic phase at accessible pressures.

cond-mat.str-el↗

arXiv2025

Prediction and Synthesis of Mg$_4$Pt$_3$H$_6$: A Metallic Complex Transition Metal Hydride Stabilized at Ambient Pressure

The low-pressure stabilization of superconducting hydrides with high critical temperatures ($T_c$s) remains a significant challenge, and experimentally verified superconducting hydrides are generally constrained to a limited number of structural prototypes. Ternary transition-metal complex hydrides (hydrido complexes)-typically regarded as hydrogen storage materials-exhibit a large range of compounds stabilized at low pressure with recent predictions for high-$T_c$ superconductivity. Motivated by this class of materials, we investigated complex hydride formation in the Mg-Pt-H system, which has no known ternary hydride compounds. Guided by ab initio structural predictions, we successfully synthesized a novel complex transition-metal hydride, Mg$_4$Pt$_3$H$_6$, using laser-heated diamond anvil cells. The compound forms in a body-centered cubic structural prototype at moderate pressures between 8-25 GPa. Unlike the majority of known hydrido complexes, Mg$_4$Pt$_3$H$_6$ is metallic, with formal charge described as 4[Mg]$^{2+}$.3[PtH$_2$]$^{2-}$. X-ray diffraction (XRD) measurements obtained during decompression reveal that Mg$_4$Pt$_3$H$_6$ remains stable upon quenching to ambient conditions. Magnetic-field and temperature-dependent electrical transport measurements indicate ambient-pressure superconductivity with $T_c$ (50%) = 2.9 K, in reasonable agreement with theoretical calculations. These findings clarify the phase behavior in the Mg-Pt-H system and provide valuable insights for transition-metal complex hydrides as a new class of hydrogen-rich superconductors.

cond-mat.supr-con↗

arXiv2025

Dome-like pressure-temperature phase diagram of the cooperative Jahn--Teller distortion in NaNiO$_2$

NaNiO$_2$ is a Ni$^{3+}$-containing layered material consisting of alternating triangular networks of Ni and Na cations, separated by octahedrally-coordinated O anions. At ambient pressure, it features a collinear Jahn--Teller distortion below $T^\mathrm{JT}_\mathrm{onset}\approx480$ K, which disappears in a first-order transition on heating to $T^\mathrm{JT}_\mathrm{end}\approx500$ K, corresponding to the increase in symmetry from monoclinic to rhombohedral. It was previously studied by variable-pressure neutron diffraction [ACS Inorganic Chemistry 61.10 (2022): 4312-4321] and found to exhibit an increasing $T^\mathrm{JT}_\mathrm{onset}$ with pressure up to ~5 GPa. In this work, powdered NaNiO$_2$ was studied via variable-pressure synchrotron x-ray diffraction up to pressures of ~67 GPa at 294 K and 403 K. Suppression of the collinear Jahn--Teller ordering is observed via the emergence of a high-symmetry rhombohedral phase, with the onset pressure occurring at ~18 GPa at both studied temperatures. Further, a discontinuous decrease in unit cell volume is observed on transitioning from the monoclinic to the rhombohedral phase. These results taken together suggest that in the vicinity of the transition, application of pressure causes the Jahn--Teller transition temperature, $T^\mathrm{JT}_\mathrm{onset}$, to decrease rapidly. We conclude that the pressure-temperature phase diagram of the cooperative Jahn--Teller distortion in NaNiO$_2$ is dome-like.

cond-mat.mtrl-sci↗

arXiv2025

Pressure induced enhancement of polar distortions in a metal, and implications on the Rashba spin-splitting

Polar metals are an intriguing class of materials in which electric polarisation and metallicity can coexist within a single phase. The unique properties of polar metals challenge expectations, making way for the exploration of exotic phenomena such as unconventional magnetism, hyperferroelectric multiferroicity and developing multifunctional devices that can leverage both the materials electric polarization and its asymmetry in the spin conductivity, that arises due to the Rashba effect. Here, via a high pressure single crystal diffraction study, we report the pressure-induced enhancement of polar distortions in such a metal, Ca$_3$Ru$_2$O$_7$. Our DFT calculations highlight that naive assumptions about the linear dependency between polar distortion amplitudes and the magnitude of the Rashba spin splitting may not be generally valid.

cond-mat.str-el↗

arXiv2024

Robustness of the pyrochlore structure in rare-earth A2Ir2O7 iridates and pressure-induced structural transformation in IrO2

A comprehensive study of the structural properties of the heavily investigated rare-earth A2Ir2O7 series under extreme conditions is presented. The series is covered by studying iridates with A = Pr, Sm, Dy-Lu. Temperature- and pressure-dependent synchrotron X-ray powder diffraction experiments reveal robustness of the pyrochlore structure throughout the rare-earth series, down to 4 K and up to 20 GPa. The thermal expansivity and pressure compressibility are determined, including Debye temperature, bulk modulus and Grüneisen parameter. Temperature and pressure evolution of the fractional coordinate of oxygen at 48f Wyckoff position, the sole free atomic position parameter, is investigated and discussed regarding the antiferromagnetic ordering of the Ir magnetic moments. In addition, the pressure evolution of the crystal structure of an IrO2 minority phase is followed. The tetragonal rutile-type structure is orthorhombically distorted at 15 GPa, and the orthorhombic structure is not fully stabilised up to 20 GPa.

cond-mat.mtrl-sci↗

arXiv2023

High pressure behaviour of the magnetic van der Waals molecular framework Ni(NCS)$_2$

Two-dimensional materials offer a unique range of magnetic, electronic and mechanical properties which can be controlled by external stimuli. Pressure is a particularly important stimulus, as it can be achieved readily and can produce large responses, especially in low-dimensional materials. In this paper we explore the pressure-dependence of the structural and magnetic properties of a two-dimensional van der Waals (vdW) molecular framework antiferromagnet with ferromagnetic layers, Ni(NCS)$_2$, up to 8.4 kbar. Through a combination of X-ray and neutron diffraction analysis, we find that Ni(NCS)$_2$ is significantly more compressible than comparable vdW metal halides, and its response is anisotropic not only out of the plane, but also within the layers. Using bulk magnetisation and neutron diffraction data, we show that the ambient layered antiferromagnetic phase is maintained up to the largest investigated pressure, but with an enhanced Néel temperature, $T_\mathrm{N}$, ($ΔT_\mathrm{N} / T_\mathrm{N} = +19$ %) and a large pressure sensitivity ($Q = \frac{1}{T_\mathrm{N}} \frac{\mathrm{d}T_\mathrm{N}}{\mathrm{d}P} = +2.3$ % kbar$^{-1}$), one of the larger values of magnetic pressure responsiveness for a vdW material. Density functional theory calculations suggest that this is due to increasing three-dimensionality. These results provide some of the first insights into the pressure response of molecular framework vdW magnets and suggest investigation of other molecular framework vdW magnets might uncover contenders for future pressure-switchable devices.

cond-mat.mtrl-sci↗

arXiv2022

Comparative structural evolution under pressure of powder and single crystals of the layered antiferromagnet FePS$_3$

The layered antiferromagnet FePS$_3$ has been shown to undergo a structural transition under pressure linked to an insulator-metal transition, with two incompatible models previously proposed for the highest-pressure structure. We present a study of the high-pressure crystal structures of FePS$_3$ using both single-crystal and powder x-ray diffraction. We show that the highest pressure transition involves a collapse of the inter-planar spacing of this material, along with an increase in symmetry from a monoclinic to a trigonal structure, to the exclusion of other models. The extent of this volume collapse is shown to be sensitive to the presence of a helium pressure medium in the sample environment, indicating that consideration of such experimental factors is important for understanding high-pressure behaviours in this material.

cond-mat.str-el↗

arXiv2021

Pressure-Dependent Phase Transitions in Hybrid Improper Ferroelectric Ruddlesden-Popper Oxides

The temperature-dependent phase transitions in Ruddlesden-Popper oxides with perovskite bilayers have been under increased scrutiny in recent years due to the so-called hybrid improper ferroelectricity that some chemical compositions exhibit. However, little is currently understood about the hydrostatic pressure dependence of these phase transitions. Herein we present the results of a high-pressure powder synchrotron X-ray diffraction experiment and $ab~initio$ calculations on the bilayered Ruddlesden-Popper phases Ca$_{3}$Mn$_{2}$O$_{7}$ and Ca$_{3}$Ti$_{2}$O$_{7}$. In both compounds we observe a first-order phase transition between polar $A2_{1}am$ and non-polar $Acaa$ structures. Interestingly, we show that while the application of pressure ultimately favours a non-polar phase -- as is commonly observed for proper ferroelectrics -- regions of response exist where pressure actually acts to increase the polar mode amplitudes. The reason for this can be untangled by considering the varied response of octahedral tilts and rotations to hydrostatic pressure and their trilinear coupling with the polar instability.

cond-mat.mtrl-sci↗

arXiv2020

Pressure-induced reconstructive phase transition in Cd$_3$As$_2$

Cadmium arsenide Cd$_3$As$_2$ hosts massless Dirac electrons in its ambient-conditions tetragonal phase. We report X-ray diffraction and electrical resistivity measurements of Cd$_3$As$_2$ upon cycling pressure beyond the critical pressure of the tetragonal phase and back to ambient conditions. We find that at room temperature the transition between the low- and high-pressure phases results in large microstrain and reduced crystallite size both on rising and falling pressure. This leads to non-reversible electronic properties including self-doping associated with defects and a reduction of the electron mobility by an order of magnitude due to increased scattering. Our study indicates that the structural transformation is sluggish and shows a sizable hysteresis of over 1~GPa. Therefore, we conclude that the transition is first-order reconstructive, with chemical bonds being broken and rearranged in the high-pressure phase. Using the diffraction measurements we demonstrate that annealing at ~200$^\circ$C greatly improves the crystallinity of the high-pressure phase. We show that its Bragg peaks can be indexed as a primitive orthorhombic lattice with a_HP~8.68 A b_HP~17.15 A and c_HP~18.58 A. The diffraction study indicates that during the structural transformation a new phase with another primitive orthorhombic structure may be also stabilized by deviatoric stress, providing an additional venue for tuning the unconventional electronic states in Cd3As2.

cond-mat.mtrl-sci↗

arXiv2019

Characterization and decomposition of the natural van der Waals heterostructure SnSb2Te4 under compression

This joint experimental and theoretical study of the structural, vibrational and electrical properties of rhombohedral SnSb2Te4 at high pressure unveils the internal mechanisms of its compression. The equation of state and the internal polyhedral compressibility, the symmetry and behavior of the Raman-active modes and the electrical behavior of this topological insulator under compression have been discussed and compared with the parent binary alpha-Sb2Te3 and SnTe compounds and with related ternary compounds. Our X-ray diffraction and Raman measurements together with theoretical calculations, which include topological electron density and electronic localization function analysis, evidence the presence of an isostructural phase transition around 2 GPa and a Fermi resonance around 3.5 GPa. The Raman spectrum of SnSb2Te4 shows vibrational modes that are forbidden in rocksalt SnTe; thus showing a novel way to experimentally observe the forbidden vibrational modes of some compounds. Additionally, since SnSb2Te4 is an incipient metal, like its parent binary compounds, we establish a new criterion to identify the recently proposed metavalent bonding in complex materials when different bond characters coexist in the system. Finally, SnSb2Te4 exhibits a pressure-induced decomposition into the high-pressure phases of its parent binary compounds above 7 GPa, which is supported by an analysis of their formation enthalpies. We have framed the behavior of SnSb2Te4 within the extended orbital radii map of BA2Te4 compounds, which paves the way to understand the pressure behavior and stability ranges of other layered van der Waals-type compounds with similar stoichiometry.

cond-mat.mtrl-sci↗

arXiv2017

Structural evolution of CO2 filled pure silica LTA zeolite under high-pressure high-temperature conditions

The crystal structure of CO2 filled pure SiO2 LTA zeolite has been studied at high pressures and temperatures using synchrotron based x ray powder diffraction. Its structure consists of 13 CO2 guest molecules, 12 of them accommodated in the large alpha cages and 1 in the beta cages, giving a SiO2:CO2 stoichiometric ratio smaller than 2. The structure remains stable under pressure up to 20 GPa with a slight pressure dependent rhombohedral distortion, indicating that pressure induced amorphization is prevented by the insertion of guest species in this open framework. The ambient-temperature lattice compressibility has been determined. In situ high pressure resistive heating experiments up to 750 K allow us to estimate the thermal expansivity at 5 GPa. Our data confirm that the insertion of CO2 reverses the negative thermal expansion of the empty zeolite structure. No evidence of any chemical reaction was observed. The possibility of synthesizing a silicon carbonate at high temperatures and higher pressures is discussed in terms of the evolution of C-O and Si-O distances between molecular and framework atoms.

cond-mat.mtrl-sci↗

arXiv2016

Encoding Complexity within Supramolecular Analogues of Frustrated Magnets

At the heart of systems chemistry lies the idea that supramolecular interactions can give rise to complex and unexpected collective states that emerge on a fundamentally different lengthscale to that of the interactions themselves. While in certain cases - e.g. the self-assembly of virus-like polyhedral cages from coordination building blocks - it is possible to control emergence in a systematic manner, the development of general approaches remains a fundamental challenge in the field. In the conceptually-related domain of frustrated magnetism - where collective states give rise to exotic physics of relevance to data storage and spintronics - the task of predicting emergent behaviour is simplified through control over the geometry and form of the magnetic interactions from which complexity arises. Seeking to combine approaches from these two fields, we study here the solid phases of inorganic polymer chains assembled from non-magnetic gold(I)/silver(I) cations and cyanide anions. We show the periodic inter-chain potential encodes a supramolecular interaction that can be tuned to mimic different magnetic interactions between XY spins ("spin rotors"). Because the chains pack on a triangular lattice, the crystal structures of gold(I)/silver(I) cyanides can be interpreted in terms of the phase behaviour of triangular XY magnets. Complex magnetic states predicted for this family - including hidden quadrupolar order and emergent spin-vortex quasiparticles - are realised for the first time in the structural chemistry of these cyanide polymers. In this way we demonstrate both how simple inorganic materials might behave as structural analogues of otherwise-unrealisable "toy" spin models, and also how a theoretical understanding of those models might be used to predict and control emergent phenomena in chemical systems.

cond-mat.mtrl-sci↗