arXiv subjects

Llibertat Abad

Publications and source records attributed to Llibertat Abad.

6 recordsLinked to original sources

arXiv2026

Layer- and Field-Dependent Magnetic Order in 2D CrSBr Revealed by Pulsed Nanocalorimetry

Understanding the evolution of magnetic order in the two-dimensional limit remains a central challenge in van der Waals magnets, where thermodynamic measurements are constrained by the femtogram-scale mass of exfoliated flakes. Here, microsecond pulse-heating nanocalorimetry is used to measure the heat capacity and magnetic entropy of CrSBr flakes down to the monolayer limit. The measurements reveal the entropy landscape associated with magnetic ordering, uncovering a decreasing interlayer transition temperature toward the monolayer limit and an entropy-derived effective moment per layer that increases with thickness toward the expected spin-only scale. Thermodynamic anomalies capture a crossover from bulk-like interlayer antiferromagnetism to a regime dominated by intralayer ferromagnetic correlations. A pronounced layer-parity effect further emerges, with odd-layer samples displaying an additional high-temperature contribution associated with uncompensated magnetic layers. Under in-plane magnetic fields applied along the easy axis, antiferromagnetic order is progressively suppressed, allowing extraction of a thickness-dependent characteristic suppression field reflecting weakened interlayer exchange coupling. Entropy analysis further reveals an extended regime of magnetic fluctuations persisting well above the interlayer ordering transition. Together, these results establish nanocalorimetry as a powerful thermodynamic probe of low-dimensional magnetism, providing direct access to magnetic entropy, exchange interactions, and dimensional crossover in atomically thin van der Waals magnets.

cond-mat.mtrl-sci↗

arXiv2025

Microsecond-Pulsed Nanocalorimetry: A Scalable Approach for Ultrasensitive Heat Capacity Measurements

We introduce a nanocalorimetric technique based on microsecond-pulsed heating (μs-PHnC) that enables high-sensitivity, quasi-isothermal heat capacity measurements on nanoscale samples. Such resolution is critical for exploring thermodynamic signatures in low-dimensional materials, where conventional techniques fall short. By confining thermal excitation to microsecond timescales, this approach minimizes lateral heat diffusion, reduces heat capacity addenda to below 10^{-9} J K^{-1}, and achieves noise densities as low as 75 pJ K^{-1} Hz^{-1/2} mm^{-2}, unlocking precise thermodynamic characterization of subnanogram samples in areas as small as 30 x 30 μm^{2}. The method delivers exceptional temperature homogeneity, as demonstrated by resolving sharp phase transitions, such as the antiferromagnetic transition in ultrathin CoO films, with unprecedented clarity. Its quasi-static operation is inherently compatible with external stimuli, including magnetic and electric fields, thereby expanding its utility for in-operando thermodynamic studies. This advancement establishes a robust and scalable platform for probing thermal phenomena in nanostructured and low-dimensional materials, significantly broadening the scope of nanocalorimetry.

cond-mat.mtrl-sci↗

arXiv2023

Wireless magneto-ionics: voltage control of magnetism by bipolar electrochemistry

Modulation of magnetic properties through voltage-driven ion motion and redox processes, i.e., magneto-ionics, is a unique approach to control magnetism with electric field for low-power memory and spintronic applications. So far, magneto-ionics has been achieved through direct electrical connections to the actuated material. Here we evidence that an alternative way to reach such control exists in a wireless manner. Induced polarization in the conducting material immersed in the electrolyte, without direct wire contact, promotes wireless bipolar electrochemistry, an alternative pathway to achieve voltage-driven control of magnetism based on the same electrochemical processes involved in direct-contact magneto-ionics. A significant tunability of magnetization is accomplished for cobalt nitride thin films, including transitions between paramagnetic and ferromagnetic states. Such effects can be either volatile or non-volatile depending on the electrochemical cell configuration. These results represent a fundamental breakthrough that may inspire future device designs for applications in bioelectronics, catalysis, neuromorphic computing, or wireless communications.

cond-mat.mtrl-sci↗

arXiv2020

Nitrogen magneto-ionics

So far, magneto-ionics, understood as voltage-driven ion transport in magnetic materials, has largely relied on controlled migration of oxygen ion/vacancy and, to a lesser extent, lithium and hydrogen. Here, we demonstrate efficient, room-temperature, voltage-driven nitrogen transport (i.e., nitrogen magneto-ionics) by electrolyte-gating of a single CoN film (without an ion-reservoir layer). Nitrogen magneto-ionics in CoN is compared to oxygen magneto-ionics in Co3O4, both layers showing a nanocrystalline face-centered-cubic structure and reversible voltage-driven ON-OFF ferromagnetism. In contrast to oxygen, nitrogen transport occurs uniformly creating a plane-wave-like migration front, without assistance of diffusion channels. Nitrogen magneto-ionics requires lower threshold voltages and exhibits enhanced rates and cyclability. This is due to the lower activation energy for ion diffusion and the lower electronegativity of nitrogen compared to oxygen. These results are appealing for the use of magneto-ionics in nitride semiconductor devices, in applications requiring endurance and moderate speeds of operation, such as brain-inspired computing.

cond-mat.mtrl-sci↗

arXiv2020

Boosting room temperature magneto-ionics in Co3O4

Voltage control of magnetism through electric field-induced oxygen motion (magneto-ionics) could represent a significant breakthrough in the pursuit for new strategies to enhance energy efficiency in a large variety of magnetic devices, such as magnetic micro-electro-mechanical systems (MEMS), magnetic logics, spin electronics, or neuromorphic computing, i.e., envisaging ultra-low power emulation of the biological synapse. Boosting the induced changes in magnetization, magneto-ionic motion and cyclability (endurance) continue to be key challenges to turn magneto-ionic phenomena into real applications. Here, we demonstrate that, without degrading cyclability, room temperature magneto-ionic motion in electrolyte-gated paramagnetic and fairly thick (> 100 nm) Co3O4 films largely depends on the configuration used to apply the electric field. In particular, magneto-ionic effects are significantly increased both in terms of generated magnetization (6 times larger: from 118.5 to 699.2 emu cm-3) and speed (35 times faster: from 33.1 to 1170.8 emu cm-3 h-1) if the electric field is applied across a conducting buffer layer (grown underneath the Co3O4 films), instead of directly contacting Co3O4. This is attributed to a greater uniformity and strength of the applied electric field when using the conducting layer. These results may trigger the use of oxygen magneto-ionics into promising new technologies, such as magnetic MEMS or brain-inspired computing, which require endurance and moderate speeds of operation.

cond-mat.mtrl-sci↗

arXiv2017

Evidence of thermal transport anisotropy in stable glasses of vapour deposited organic molecules

Vapour-deposited organic glasses are currently in use in many optoelectronic devices. Their operation temperature is limited by the glass transition temperature of the organic layers and thermal management strategies become increasingly important to improve the lifetime of the device. Here we report the unusual finding that molecular orientation heavily influences heat flow propagation in glassy films of small molecule organic semiconductors. The thermal conductivity of vapour-deposited thin-film semiconductor glasses is anisotropic and controlled by the deposition temperature. We compare our data with extensive molecular dynamics simulations to disentangle the role of density and molecular orientation on heat propagation. Simulations do support the view that thermal transport along the backbone of the organic molecule is strongly preferred with respect to the perpendicular direction. This is due to the anisotropy of the molecular interaction strength that limit the transport of atomic vibrations. This approach could be used in future developments to implement small molecule glassy films in thermoelectric or other organic electronic devices.

cond-mat.mtrl-sci↗