arXiv subjects

Xavier Moya

Publications and source records attributed to Xavier Moya.

At least 19 recordsLinked to original sources

arXiv2025

Large electrocaloric strength in ferroelectric nematic liquid crystals with a tuneable operational temperature range

The electrocaloric (EC) effect offers a promising energy-efficient and clean cooling technology. We present the first direct measurements of EC temperature change in a new family of EC fluids, ferroelectric nematic liquid crystals (FNLCs), demonstrating in two such materials temperature jumps of $|{\Delta}T_j|$ ~ 0.2 K for field changes as low as ${\Delta}E$ ~ 0.1 $V {\mu}m^{-1}$. Indirect measurements of adiabatic temperature change $|{\Delta}T|$ confirm that these direct measurements are an underestimate and that ${\Delta}E$ = 2 $V {\mu}m^{-1}$ can induce up to $|{\Delta}T|$ ~ 1.6 K, yielding EC strengths $|{\Delta}T/{\Delta}E|$ up to 100% higher than incumbent materials. For temperature spans of 5-10 K, we predict a coefficient of performance of ~21-40. We find $|{\Delta}T|$ ~ 1 K for >100 FNLCs that collectively span all temperatures between $0{^\circ}$C and $100{^\circ}$C. This, together with the new device concepts conceivable with fluid EC materials, offers huge potential for cooling applications.

cond-mat.soft↗

arXiv2025

Enhanced reversible barocaloric effect at low pressure in neopentyl plastic crystal solid solutions

The discovery of colossal barocaloric effects in neopentyl glycol (NPG) makes plastic crystals promising candidates for solid-state refrigerants with lower environmental impact than vapour compression fluids. Optimising operational temperatures and low-pressure operability remains challenging without compromising thermodynamic parameters. Here, we implement a strategy to improve the viability of NPG derivatives as barocaloric refrigerants. We blend pentaglycerine (PG) with NPG to lower the phase transition temperature, then dope the blend with 2% pentaerythritol (PE) to improve transition reversibility. In comparison with NPG under the same conditions, this ternary system has a seven-fold increase in reversible isothermal entropy change (|$\Delta S_{(it,rev)}$ | = 13.4 J kg$^{-1}$ K$^{-1}$) and twenty-fold increase in operational temperature span ($\Delta T_{span}$ = 18 K) at pressures of 1 kbar. Synchrotron x-ray diffraction and quasielastic neutron scattering reveal structural and dynamical effects that broaden the temperature range of the first-order phase transition due to intermolecular hydrogen bond network disruption by the molecular dopants. We propose that exploiting the compositional phase space of multi-component molecular blends is effective for designing practicable molecular BCs.

cond-mat.mtrl-sci↗

arXiv2024

Direct observation of thermal hysteresis in the molecular dynamics of barocaloric neopentyl glycol

Barocalorics (BCs) are emerging as promising alternatives to vapour-phase refrigerants, which are problematic as they exacerbate climate change when they inevitably leak into the atmosphere. However, the commercialisation of BC refrigerants is significantly hindered by hysteresis in the solid-solid phase transition that would be exploited in a refrigeration cycle. Here, we provide new insight into the hysteresis that is a critical step towards the rational design of viable BCs. By studying the benchmark BC plastic crystal, neopentyl glycol (NPG), we observe directly the liberation of the hydroxyl rotational modes that unlock the hydrogen bond network, distinguishing for the first time the molecular reorientation and hydroxymethyl rotational modes. We showcase the use high-resolution inelastic fixed-window scans in combination with quasielastic neutron scattering (QENS) measurements to build a comprehensive microscopic understanding of the NPG phase transition, directly tracking the molecular dynamics of the phase transition. Hysteresis previously observed in calorimetric studies of NPG is now observed directly as hysteresis in molecular rotational modes, and hence in the formation and disruption of hydrogen bonding. Furthermore, by tracking the thermal activation of three main reorientation modes, we suggest that their fractional excitations may resolve an outstanding discrepancy between measured and calculated entropy change. These results allow for direct study of the molecular dynamics that govern the thermal hysteresis of small molecule energy materials. They will be broadly applicable, as many promising BC material families possess first-order transitions involving molecular reorientations.

cond-mat.mtrl-sci↗

arXiv2020

Suppression of acoustic emission during superelastic tensile cycling of polycrystalline Ni$_{50.4}$Ti$_{49.6}$

We investigate acoustic emission (AE) that arises during the martensitic transition in a polycrystalline specimen of the prototypical superelastic/elastocaloric alloy Ni$_{50.4}$Ti$_{49.6}$ (at. %) driven using tensile strain. We use two independent AE sensors in order to locate AE events, and focus on contributions to the AE that arise away from the grips of the mechanical testing machine. Significant AE activity is present during the first mechanical loading primarily due to nucleation and growth of wide Lüders-like bands during the forward martensitic transition (imaged using visible light and infrared (IR) radiation) that lead to persistent changes in intergranular interactions. AE activity is suppressed during the subsequent reverse martensitic transition on unloading, and in successive loading/unloading cycles, for which the Lüders-like bands narrow and modify intergranular interactions to much less extent. After the first loading, we find that the AE activity associated with the martensitic transition is weak, and we suggest that this is because the elastic anisotropy and strain incompatibility in Ni-Ti are low. We also find that the AE activity becomes weaker on mechanically cycling due to increased retained martensite.

cond-mat.mtrl-sci↗

arXiv2020

Large magnetoelectric coupling in multiferroic oxide heterostructures assembled via epitaxial lift-off

The strain dependent functional properties of epitaxial transition metal oxide films can be significantly modified via substrate selection. However, large lattice mismatches preclude dislocation-free epitaxial growth on ferroelectric substrates, whose strain states are modified by applied electric fields. Here we overcome this mismatch problem by depositing an epitaxial film of ferromagnetic La0.7Sr0.3MnO3 on a single crystal substrate of well lattice matched SrTiO3 via a film of SrRuO3 that we subsequently dissolved, permitting the transfer of unstrained La0.7Sr0.3MnO3 to a ferroelectric substrate of 0.68Pb(Mg1/3Nb2/3)O3 0.32PbTiO3 in a different crystallographic orientation. Ferroelectric domain switching, and a concomitant ferroelectric phase transition, produced large non volatile changes of magnetization that were mediated by magnetic domain rotations at locations defined by the microstructure - as revealed via high resolution vector maps of magnetization constructed from photoemission electron microscopy data, with contrast from x-ray magnetic circular dichroism. In future, our method may be exploited to control functional properties in dislocation free epitaxial films of any composition.

cond-mat.mtrl-sci↗

arXiv2020

High-contrast imaging of 180° ferroelectric domains by optical microscopy using ferroelectric liquid crystals

Ferroelectric liquid crystals (FLCs) couple the direction of their spontaneous electric polarization to the direction of tilt of their optic axis. Consequently, reversal of the electric polarization by an electric field gives rise to an immediate and lasting optical response when an appropriately aligned FLC is observed between crossed polarizers, with one field direction yielding a dark image, and the opposite direction yielding a bright image. Here this peculiar electro-optic response is used to image, with high optical contrast, 180° ferroelectric domains in a crystalline substrate of magnesium-doped lithium niobate. The lithium niobate substrate contains a few domains with upwards electric polarization surrounded by regions with downward electric polarization. In contrast to a reference non-chiral liquid crystal that is unable to show ferroelectric behavior due to its high symmetry, the FLC, which is used as a thin film confined between the lithium niobate substrate and an inert aligning substrate, reveals ferroelectric domains as well as their boundaries, with strong black and white contrast. The results show that FLCs can be used for non-destructive read-out of domains in underlying ferroelectrics, with potential applications in e.g. photonic devices and non-volatile ferroelectric memories.

cond-mat.mtrl-sci↗

arXiv2019

Colossal barocaloric effects near room temperature in plastic crystals of neopentylglycol

There is currently great interest in replacing the harmful volatile hydrofluorocarbon fluids used in refrigeration and air-conditioning with solid materials that display magnetocaloric, electrocaloric or mechanocaloric effects. However, the field-driven thermal changes in all of these caloric materials fall short with respect to their fluid counterparts. Here we show that plastic crystals of neopentylglycol (CH3)2C(CH2OH)2 display unprecedentedly large pressure-driven thermal changes near room temperature due to molecular reconfiguration, and that these changes are comparable with those exploited commercially in hydrofluorocarbons. Our discovery of colossal barocaloric effects in a plastic crystal should bring barocaloric materials to the forefront of research and development in order to achieve safe environmentally friendly cooling without compromising performance.

cond-mat.mtrl-sci↗

arXiv2018

Multi-site exchange enhanced barocaloric response in Mn$_{3}$NiN

We have studied the barocaloric effect (BCE) in the geometrically frustrated antiferromagnet Mn$_{3}$NiN across the Néel transition temperature. Experimentally we find a larger barocaloric entropy change by a factor of 1.6 than that recently discovered in the isostructural antiperovskite Mn$_{3}$GaN despite greater magnetovolume coupling in the latter. By fitting experimental data to theory we show that the larger BCE of Mn$_{3}$NiN originates from multi-site exchange interactions amongst the local Mn magnetic moments and their coupling with itinerant electron spins. Using this framework, we discuss the route to maximise the BCE in the wider Mn$_{3}$AN family.

cond-mat.str-el↗

arXiv2012

A ferroelectric memristor

Memristors are continuously tunable resistors that emulate synapses. Conceptualized in the 1970s, they traditionally operate by voltage-induced displacements of matter, but the mechanism remains controversial. Purely electronic memristors have recently emerged based on well-established physical phenomena with albeit modest resistance changes. Here we demonstrate that voltage-controlled domain configurations in ferroelectric tunnel barriers yield memristive behaviour with resistance variations exceeding two orders of magnitude and a 10 ns operation speed. Using models of ferroelectric-domain nucleation and growth we explain the quasi-continuous resistance variations and derive a simple analytical expression for the memristive effect. Our results suggest new opportunities for ferroelectrics as the hardware basis of future neuromorphic computational architectures.

cond-mat.mtrl-sci↗

arXiv2009

Lattice dynamics in magnetic superelastic Ni-Mn-In alloys. Neutron scattering and ultrasonic experiments

Neutron scattering and ultrasonic methods have been used to study the lattice dynamics of two single crystals of Ni-Mn-In Heusler alloys close to Ni$_{50}$Mn$_{34}$In$_{16}$ magnetic superelastic composition. The paper reports the experimental determination of the low-lying phonon dispersion curves and the elastic constants for this alloy system. We found that the frequencies of the TA$_{2}$ branch are relatively low and it exhibits a small dip anomaly at a wave number $ξ_{0} \approx 1/3$, which softens with decreasing temperature. Associated with the softening of this phonon, we also observed the softening of the shear elastic constant $C'=(C_{11}-C_{12})/2$. Both temperature softenings are typical for bcc based solids which undergo martensitic transformations and reflect the dynamical instability of the cubic lattice against shearing of $\{110\}$ planes along $<1\bar{1}0>$ directions. Additionally, we measured low-lying phonon dispersion branches and elastic constants in applied magnetic fields aimed to characterize the magnetoelastic coupling.

cond-mat.mtrl-sci↗

arXiv2008

Phase diagram of Fe-doped Ni-Mn-Ga ferromagnetic shape-memory alloys

We have studied the effect of Fe addition on the structural and magnetic transitions in the magnetic shape memory alloy Ni-Mn-Ga by substituting systematically each atomic species by Fe. Calorimetric and AC susceptibility measurements have been carried out in order to study the magnetic and structural transformation properties. We find that the addition of Fe modifies the structural and magnetic transformation temperatures. Magnetic transition temperatures are displaced to higher values when Fe is substituted into Ni-Mn-Ga, while martensitic and premartensitic transformation temperatures shift to lower values. Moreover, it has been found that the electron per atom concentration essentially governs the phase stability in the quaternary system. However, the observed scaling of transition temperatures with $e/a$ differs from that reported in the related ternary system Ni-Mn-Ga.

cond-mat.mtrl-sci↗

arXiv2007

Effects of hydrostatic pressure on the magnetism and martensitic transition of Ni-Mn-In magnetic superelastic alloys

We report magnetization and differential thermal analysis measurements as a function of pressure accross the martensitic transition in magnetically superelastic Ni-Mn-In alloys. It is found that the properties of the martensitic transformation are significantly affected by the application of pressure. All transition temperatures shift to higher values with increasing pressure. The largest rate of temperature shift with pressure has been found for Ni$_{50}$Mn$_{34}$In$_{16}$ as a consequence of its small entropy change at the transition. Such a strong pressure dependence of the transition temperature opens up the possibility of inducing the martensitic transition by applying relatively low hydrostatic pressures.

cond-mat.mtrl-sci↗

arXiv2007

Tailoring magnetic and magnetocaloric properties of martensitic transitions in ferromagnetic Heusler alloys

Ni$_{50}$Mn$_{34}$In$_{16}$ undergoes a martensitic transformation around 250 K and exhibits a field induced reverse martensitic transformation and substantial magnetocaloric effects. We substitute small amounts Ga for In, which are isoelectronic, to carry these technically important properties to close to room temperature by shifting the martensitic transformation temperature.

cond-mat.mtrl-sci↗

arXiv2007

Magnetization easy-axis in martensitic Heusler alloys estimated by strain measurements under magnetic-field

We study the temperature dependence of strain under constant magnetic-fields in Ni-Mn based ferromagnetic Heusler alloys in the form Ni-Mn-$X$ ($X$: Ga, In, Sn, Sb) which undergo a martensitic transformation. We discuss the influence of the applied magnetic-field on the nucleation of ferromagnetic martensite and extract information on the easy-axis of magnetization in the martensitic state.

cond-mat.mtrl-sci↗

arXiv2007

Effect of Co and Fe on the inverse magnetocaloric properties of Ni-Mn-Sn

At certain compositions Ni-Mn-$X$ Heusler alloys ($X$: group IIIA-VA elements) undergo martensitic transformations, and many of them exhibit inverse magnetocaloric effects. In alloys where $X$ is Sn, the isothermal entropy change is largest among the Heusler alloys, particularly in Ni$_{50}$Mn$_{37}$Sn$_{13}$ where it reaches a value of 20 Jkg$^{-1}$K$^{-1}$ for a field of 5T. We substitute Ni with Fe and Co in this alloy, each in amounts of 1 at% and 3 at% to perturb the electronic concentration and examine the resulting changes in the magnetocaloric properties. Increasing both Fe and Co concentrations causes the martensitic transition temperature to decrease, whereby the substitution by Co at both compositions or substituting 1 at% Fe leads to a decrease in the magnetocaloric effect. On the other hand, the magnetocaloric effect in the alloy with 3 at% Fe leads to an increase in the value of the entropy change to about 30 Jkg$^{-1}$K$^{-1}$ at 5T.

cond-mat.mtrl-sci↗

arXiv2007

Magnetic superelasticity and inverse magnetocaloric effect in Ni-Mn-In

Applying a magnetic field to a ferromagnetic Ni$_{50}$Mn$_{34}$In$_{16}$ alloy in the martensitic state induces a structural phase transition to the austenitic state. This is accompanied by a strain which recovers on removing the magnetic field giving the system a magnetically superelastic character. A further property of this alloy is that it also shows the inverse magnetocaloric effect. The magnetic superelasticity and the inverse magnetocaloric effect in Ni-Mn-In and their association with the first order structural transition is studied by magnetization, strain, and neutron diffraction studies under magnetic field.

cond-mat.mtrl-sci↗

arXiv2007

Cooling and heating by adiabatic magnetization in the Ni$_{50}$Mn$_{34}$In$_{16}$ magnetic shape memory alloy

We report on measurements of the adiabatic temperature change in the inverse magnetocaloric Ni$_{50}$Mn$_{34}$In$_{16}$ alloy. It is shown that this alloy heats up with the application of a magnetic field around the Curie point due to the conventional magnetocaloric effect. In contrast, the inverse magnetocaloric effect associated with the martensitic transition results in the unusual decrease of temperature by adiabatic magnetization. We also provide magnetization and specific heat data which enable to compare the measured temperature changes to the values indirectly computed from thermodynamic relationships. Good agreement is obtained for the conventional effect at the second-order paramagnetic-ferromagnetic phase transition. However, at the first order structural transition the measured values at high fields are lower than the computed ones. Irreversible thermodynamics arguments are given to show that such a discrepancy is due to the irreversibility of the first-order martensitic transition.

cond-mat.mtrl-sci↗

arXiv2006

Temperature and magnetic field dependences of the elastic constants of Ni-Mn-Al magnetic Heusler alloys

We report on measurements of the adiabatic second order elastic constants of the off-stoichiometric Ni$_{54}$Mn$_{23}$Al$_{23}$ single crystalline Heusler alloy. The variation in the temperature dependence of the elastic constants has been investigated across the magnetic transition and over a broad temperature range. Anomalies in the temperature behaviour of the elastic constants have been found in the vicinity of the magnetic phase transition. Measurements under applied magnetic field, both isothermal and variable temperature, show that the value of the elastic constants depends on magnetic order, thus giving evidence for magnetoelastic coupling in this alloy system.

cond-mat.mtrl-sci↗