arXiv subjects

Trevor A. Tyson

Publications and source records attributed to Trevor A. Tyson.

16 recordsLinked to original sources

arXiv2026

Magnetic field induced modification of a first-order ferromagnetic transition in Eu2In

We present a comprehensive study of the temperature- and magnetic-field-dependent magnetization, specific heat, and local crystal structure across the first-order ferromagnetic-paramagnetic transition in Eu$_2$In. Anomalies in the magnetocaloric response are observed near $H \approx 25$~kOe, including changes in field scaling of magnetic entropy, local entropy exponent, and universal master curve, which suggest an apparent weakening of the first-order character of the transition. However, quantitative analysis of the magnetocaloric parameters together with modified Arrott plots demonstrates that the transition remains first order up to at least 70~kOe. Specific-heat measurements reveal a field-induced splitting of the sharp zero-field anomaly into a doublet, providing a natural explanation for the change in the magnetocaloric response. Magnetic field dependent extended x-ray absorption fine structure (EXAFS) measurements show no detectable field-induced changes in the local coordination environment of Eu. We therefore attribute these observations to a magnetic field induced two-step transition process in Eu$_2$In.

physics.app-ph↗

arXiv2024

Origin of Pressure-Induced Structural Instability in CsPbX$_3$ Photovoltaic Perovskites

Under external stimuli, lead halide perovskites exhibit large atomic fluctuations, impacting optical and electron transport properties that affect device performance in operational settings. However, a thorough understanding of the atomic basis for the underlying structural instability is still absent. Focusing on the model material CsPbBr$_3$, the inherent lattice softness of halide perovskites is elucidated at the atomic level through in-situ single-crystal X-ray diffraction measurements under pressure complemented by atomic level simulations. We identify and explore the nature of the first-order phase transition to a distorted P21/c phase at 1.3 GPa, induced by the sudden Cs-Br bonds breaking. Unlike classical transition metal oxide perovskites, where the internal energy term dominates, we show explicitly that pressure primarily influences the Gibbs free energy for halide perovskites through the pressure-volume term. As such, strategically mitigating bond strains from volume shrinkage is the key to suppressing the first-order behavior for maintaining the coordinates of PbX$_6$ polyhedral upon external perturbation. Our thermodynamic calculation reveals the demand for high entropy in the -T*del-S term, which can be achieved by exploring a broader spectrum of doped A site and B sites in ABX$_3$ systems, enabling continuous structural changes that facilitate recovery from mechanical damage in practical applications.

cond-mat.mtrl-sci↗

arXiv2016

Size-Dependent Structural Phase Transitions in SrTiO3 Nanoparticles

Understanding the structural phase diagram of nano scale SrTiO3 has important implications on the basic physics and applications of the general class of transition metal oxide perovskites. Pressure dependent structural measurements on monodispersed nanoscale SrTiO3 samples with average diameters of 10 to ~80 nm were conducted. A robust pressure independent polar structure was detected in the 10 nm sample for pressures of up to 13 GPa while a size dependent cubic to tetragonal transition occurs (at P = Pc) for larger particle sizes. The results suggest that the growth of ~10 nm STO particles on substrates with large lattice mismatch will not alter the polar state of the system for a large range of strain values, possibly enabling device use.

cond-mat.mtrl-sci↗

arXiv2015

Unveiling hidden ferrimagnetism and giant magnetoelectricity in polar magnet Fe2Mo3O8

Magnetoelectric (ME) effect is recognized for its utility for low-power electronic devices.Largest ME coefficients are often associated with phase transitions in which ferroelectricity is induced by magnetic order. Unfortunately, in these systems, large ME response is revealed only upon elaborate poling procedures. These procedures may become unnecessary in single-polar-domain crystals of polar magnets. Here we report giant ME effects in a polar magnet Fe2Mo3O8 at temperatures as high as 60 K.Polarization jumps of 0.3 μC/cm2, and repeated mutual control of ferroelectric and magnetic moments with differential ME coefficients on the order of 10$^4$ ps/m are achieved.Importantly, no electric or magnetic poling is needed, as necessary for applications.The sign of the ME coefficients can be switched by changing the applied "bias" magnetic field. The observed effects are associated with a hidden ferrimagnetic order unveiled by application of a magnetic field.

cond-mat.mtrl-sci↗

arXiv2014

Polar State in Freestanding Strontium Titanate Nanoparticles

Monodispersed strontium titanate nanoparticles were prepared and studied in detail. It is found that ~10 nm as-prepared stoichiometric nanoparticles are in a polar structural state (with possibly ferroelectric properties) over a broad temperature range. A tetragonal structure, with possible reduction of the electronic hybridization is found as the particle size is reduced. In the 10 nm particles, no change in the local Ti-off centering is seen between 20 and 300 K. The results indicate that nanoscale motifs of SrTiO3 may be utilized in data storage as assembled nano-particle arrays in applications where chemical stability, temperature stability and low toxicity are critical issues.

cond-mat.mtrl-sci↗

arXiv2012

A Structural Phase Transition in Ca3Co4O9 Associated with Enhanced High Temperature Thermoelectric Properties

Temperature dependent electrical resistivity, crystal structure and heat capacity measurements reveal a resistivity drop and metal to semiconductor transition corresponding to first order structural phase transition near 400 K in Ca3Co4O9. The lattice parameter c varies smoothly with increasing temperature, while anomalies in the a, b1 and b2 lattice parameters occur at ~ 400 K. Both Ca2CoO3 and CoO2 layers become distorted above ~ 400 K associated with the metal to semiconductor transport behavior change. Resistivity and heat capacity measurements as a function of temperature under magnetic field indicates low spin contribution to this transition. Reduced resistivity associated with this first order phase transition from metallic to semiconducting behavior enhances the thermoelectric properties at high temperatures and points to the metal to semiconductor transition as a mechanism for improved ZT in high temperature thermoelectric oxides.

cond-mat.mtrl-sci↗

arXiv2010

Bulk magnetic order in a two dimensional Ni1+/Ni2+ (d9/d8) nickelate, isoelectronic with superconducting cuprates

Bulk magnetic order in two dimensional La4Ni3O8 nickelate with Ni1+/Ni2+ (d9/d8), isoelectronic with superconducting cuprates is demonstrated experimentally and theoretically. Magnetization, specific heat and 139La NMR evidence a transition at 105 K to an antiferromagnetic state. Theoretical calculations by DFT relate the transition to a nesting instability of the Fermi surface with ordering wave-vector Q = [1/3, 1/3, 0].

cond-mat.str-el↗

arXiv2008

Pressure Effects on the Atomic and Electronic Structure of Aligned Small Diameter Carbon Nanotubes

Density functional methods have been used to calculate the electronic properties of aligned smalldiameter single-walled carbon nanotubes under hydrostatic pressures. Abrupt pressure induced semiconductor-metal and metal-semiconductor transitions concomitant with changes in structure are observed. Novel and unexpected unit cell nanotube cross-sections are found. These tubes are observed to form interlinking structures at very high pressures. The large changes in electronic structure and the ability of different small diameter nanotubes to respond in different pressure regimes suggest their use in high pressure multiple switching devices.

cond-mat.mtrl-sci↗

arXiv2007

Observation of Ferromagnetic Clusters in Bi0.125Ca0.875MnO3

The electron doped manganite system, Bi0.125Ca0.875MnO3, exhibits large bulk magnetization of unknown origin. To select amongst possible magnetic ordering models, we have conducted temperature and magnetic field dependent small-angle neutron scattering measurements. Nontrivial spin structure has been revealed. Ferromagnetic spin clusters form in the antiferromagnetic background when temperature is decreased to Tc~108K. With a further reduction in temperature or the application of external magnetic field, the clusters begin to form in larger numbers, which gives an overall enhancement of magnetization below Tc.

cond-mat.mtrl-sci↗

arXiv2004

The structure and stability of beta-Ta thin films

Ta films with tetragonal crystalline structure (beta-phase), deposited by magnetron sputtering on different substrates (steel, silicon and silicon dioxide), have been studied. In all cases, very highly preferred (001) orientation was observed in x-ray diffraction (XRD) measurements. All diffraction data revealed two weak reflections corresponding to d-spacing of 0.5272 and 0.1777 nm. The presence of the two peaks, attributed to (001) and (003) reflections, indicates that beta-Ta films exhibit a high preference for the space group of P-421m over P42/mnm, previously proposed for beta-Ta. Differences in relative intensities of (00l) reflections, calculated for single crystal beta-Ta sigma-type Frank-Kasper structure and those measured in the films, are attributed to defects in the films. Molecular dynamics simulations performed on tantalum clusters with six different initial configurations using the embedded-atom-method (EAM) potential revealed the stability of beta-Ta, which might explain its growth on many substrates under various deposition conditions.

cond-mat.mtrl-sci↗

arXiv2003

Transport and structural study of pressure-induced magnetic states in Nd0.55Sr0.45MnO3 and Nd0.5Sr0.5MnO3

Pressure effects on the electron transport and structure of Nd1-xSrxMnO3 (x = 0.45, 0.5) were investigated in the range from ambient to ~6 GPa. In Nd0.55Sr0.45MnO3, the low-temperature ferromagnetic metallic state is suppressed and a low temperature insulating state is induced by pressure. In Nd0.5Sr0.5MnO3, the CE-type antiferromagnetic charge-ordering state is suppressed by pressure. Under pressure, both samples have a similar electron transport behavior although their ambient ground states are much different. It is surmised that pressure induces an A-type antiferromagnetic state at low temperature in both compounds.

cond-mat↗

arXiv2003

Pressure effects on charge, spin, and metal-insulator transitions in narrow bandwidth manganite Pr$_{1-x}$Ca$_{x}$MnO$_{3}$

Pressure effects on the charge and spin states and the relation between the ferromagnetic and metallic states were explored on the small bandwidth manganite Pr$_{1-x}$Ca$_{x}$MnO$_{3}$ (x = 0.25, 0.3, 0.35). Under pressure, the charge ordering state is suppressed and a ferromagnetic metallic state is induced in all three samples. The metal-insulator transition temperature (T$_{MI}$) increases with pressure below a critical point P*, above which T$_{MI}$ decreases and the material becomes insulating as at the ambient pressure. The e$_{g}$ electron bandwidth and/or band-filling mediate the pressure effects on the metal-insulator transition and the magnetic transition. In the small bandwidth and low doping concentration compound (x = 0.25), the T$_{MI}$ and Curie temperature (T$_{C}$) change with pressure in a reverse way and do not couple under pressure. In the x = 0.3 compound, the relation of T$_{MI}$ and T$_{C}$ shows a critical behavior: They are coupled in the range of $\sim$0.8-5 GPa and decoupled outside of this range. In the x = 0.35 compound, T$_{MI}$ and T$_{C}$ are coupled in the measured pressure range where a ferromagnetic state is present.

cond-mat↗

arXiv2003

Correlations between pressure and bandwidth effects in metal-insulator transitions in manganites

The effect of pressure on the metal-insulator transition in manganites with a broad range of bandwidths is investigated. A critical pressure is found at which the metal-insulator transition temperature, T$_{MI}$, reaches a maximum value in every sample studied. The origin of this universal pressure and the relation between the pressure effect and the bandwidth on the metal-insulator transition are discussed.

cond-mat↗

arXiv2003

Pressure Induced Reentrant Electronic and Magnetic State in Pr0.7Ca0.3MnO3 Manganite

In Pr$_{0.7}$Ca$_{0.3}$MnO$_{3}$, pressure induces reentrant magnetic and electronic state changes in the range 1 atm to $\sim$ 6 GPa. The metal-insulator and magnetic transition temperatures coincide from $\sim$1 to 5 GPa, decouple outside of this range and do not change monotonically with pressure. The effects may be explained by pressure tuned competition between double exchange and super exchange. The insulating state induced by pressure above $\sim$5 GPa is possibly ferromagnetic, different from the ferromagnetic and antiferromagnetic phase-separated insulating state below $\sim$0.8 GPa.

cond-mat↗

arXiv2003

Effects of Pressure on Electron Transport and Local Structure of Manganites: Low to High Pressure Regime

The pressure dependence of the resistivity and structure of La0.60Y0.07Ca0.33MnO3 has been explored in the pressure range from 1 atm to ~7 GPa. The metal to insulator transition temperature (TMI) was found to reach a maximum and the resistivity achieves a minimum at ~3.8 GPa. Beyond this pressure, TMI is reduced with a concomitant increase in the resistivity. Structural measurements at room temperature show that at low pressure (below 2 GPa) the Mn-O bond lengths are compressed. Between ~2 and ~4 GPa, a pressure induced enhancement of the Jahn-Teller (JT) distortion occurs in parallel with an increase in Mn-O1-Mn bond angle to ~180 (degree). Above ~4 GPa, the Mn-O1-Mn bond angle is reduced while the JT distortion appears to remain unchanged. The resistivity above TMI is well modeled by variable range hopping. The pressure dependence of the localization length follows the behavior of TMI.

cond-mat.mtrl-sci↗

arXiv2002

Investigation of the structure of beta-Tantalum

The local structure of beta-tantalum was investigated by comparing experimental extended x-ray absorption fine structure (EXAFS) measurements with calculated spectra of proposed models. Four possible structure candidates were examined: a beta-Uranium based structure, a distorted A15 structure, a bcc-Ta based superlattice structure with N interstitials and a simple hcp structure. The local structural measurements were found to be consistent with the beta-Uranium based model containing 30 atoms per unit cell and having the space group P42/mnm. The thermal effect analysis on x-ray diffraction and EXAFS spectra, which reveals that beta-Ta is highly disordered, agrees with the low symmetry and anisotropic system of the beta-U model.

cond-mat↗