arXiv subjects

Alberto Quintana

Publications and source records attributed to Alberto Quintana.

12 recordsLinked to original sources

arXiv2026

Light-modulated exchange bias in multiferroic heterostructures

Magnetic straintronics, the strain-mediated control of magnetic anisotropy, has emerged as a key direction for next-generation energy-efficient technologies. In multiferroic heterostructures, magnetoelectric coupling is typically achieved by applying an electric field on a ferroelectric phase, inducing strain through the converse piezoelectric effect, which is then transferred to the adjacent ferromagnetic phase. As an alternative, strain can be remotely modulated through the photostrictive effect induced by light. While light-driven control of magnetic anisotropy has been explored, optical modulation of more complex phenomena such as exchange bias remains largely unaddressed. Here, we demonstrate significant light-induced modulation of exchange bias and magnetization switching at room temperature in a Pb(Mg1/3Nb2/3)O3-Pb(Zr,Ti)O3 (PMN-PZT)/Fe80Ga20(FeGa)/Ir20Mn80(IrMn) multiferroic heterostructure, driven by visible-light-photostriction. The magnetization state correlates with the light intensity, enabling multi-level states with light power densities as low as 0.1 W cm-2. These findings suggest a promising route toward low-power, multistate, and wireless opto-magnetic memory applications.

cond-mat.mtrl-sci↗

arXiv2025

Carbon magneto-ionics: Control of magnetism through voltage-driven carbon transport

Control of magnetism through voltage-driven ionic processes (i.e., magneto-ionics) holds potential for next-generation memories and computing. This stems from its non-volatility, flexibility in adjusting the magnitude and speed of magnetic modulation, and energy efficiency. Since magneto-ionics depends on factors like ionic radius and electronegativity, identifying alternative mobile ions is crucial to embrace new phenomena and applications. Here, the feasibility of C as a prospective magneto-ionic ion is investigated in a Fe-C system by electrolyte gating. In contrast to most magneto-ionic systems, Fe-C presents a dual-ion mechanism: Fe and C act as cation and anion, respectively, moving uniformly in opposite directions under an applied electric field. This leads to a 7-fold increase in saturation magnetization with magneto-ionic rates larger than 1 emu cm-3 s-1, and a 25-fold increase in coercivity. Since carbides exhibit minimal cytotoxicity, this introduces a biocompatible dimension to magneto-ionics, paving the way for the convergence of spintronics and biotechnology.

cond-mat.mtrl-sci↗

arXiv2025

Charge-transfer-mediated boron magneto-ionics: Towards voltage-driven multi-ion transport

Voltage control of magnetism via magneto-ionics, where ion transport and/or redox processes drive magnetic modulation, holds great promise for next-generation memories and computing. This stems from its non-volatility and ability to precisely tune both the magnitude and speed of magnetic properties in an energy-efficient manner. However, expanding magneto-ionics to incorporate novel mobile ions or even multiple ion species is crucial for unlocking new phenomena and enabling multifunctional capabilities. Here, we demonstrate voltage-driven multi-ion transport in a FeBO system with increasing oxygen content, progressively transitioning from an electrostatic-like response to a more pronounced electrochemical (magneto-ionic) behavior. The voltage-driven transport of both B and Fe is activated by oxidation state tuning, owing to the larger electronegativity of oxygen. Such charge-transfer effects allow multi-ion magneto-ionics, where O ions move oppositely to Fe and B ions. These results pave the way for programmable functionalities by leveraging elements with different electron affinities through charge-transfer engineering.

cond-mat.mtrl-sci↗

arXiv2023

Nitrogen-Based Magneto-Ionic Manipulation of Exchange Bias in CoFe/MnN Heterostructures

Electric field control of the exchange bias effect across ferromagnet/antiferromagnet (FM/AF) interfaces has offered exciting potentials for low-energy-dissipation spintronics. In particular, the solid state magneto-ionic means is highly appealing as it may allow reconfigurable electronics by transforming the all-important FM/AF interfaces through ionic migration. In this work, we demonstrate an approach that combines the chemically induced magneto-ionic effect with the electric field driving of nitrogen in the Ta/Co$_{0.7}$Fe$_{0.3}$/MnN/Ta structure to electrically manipulate exchange bias. Upon field-cooling the heterostructure, ionic diffusion of nitrogen from MnN into the Ta layers occurs. A significant exchange bias of 618 Oe at 300 K and 1484 Oe at 10 K is observed, which can be further enhanced after a voltage conditioning by 5% and 19%, respectively. This enhancement can be reversed by voltage conditioning with an opposite polarity. Nitrogen migration within the MnN layer and into the Ta capping layer cause the enhancement in exchange bias, which is observed in polarized neutron reflectometry studies. These results demonstrate an effective nitrogen-ion based magneto-ionic manipulation of exchange bias in solid-state devices.

physics.app-ph↗

arXiv2022

Hydroxide-based magneto-ionics: electric-field control of reversible paramagnetic-to-ferromagnetic switch in $α$-Co(OH)$_{2}$ films

Magneto-ionics has emerged as a promising approach to manipulate magnetic properties, not only by drastically reducing power consumption associated with electric current based devices but also by enabling novel functionalities. To date, magneto-ionics have been mostly explored in oxygen-based systems, while there is a surge of interests in alternative ionic systems. Here we demonstrate highly effective hydroxide-based magneto-ionics in electrodeposited $α$-Co(OH)$_{2}$ films. The $α$-Co(OH)$_{2}$, which is a room temperature paramagnet, is switched to ferromagnetic after electrolyte gating with a negative voltage. The system is fully, magnetically reversible upon positive voltage application. The origin of the reversible paramagnetic-to-ferromagnetic transition is attributed to the ionic diffusion of hydroxyl groups, promoting the formation of metallic cobalt ferromagnetic regions. Our findings demonstrate one of the lowest turn-on voltages reported for propylene carbonate gated experiments. By tuning the voltage magnitude and sample area we demonstrate that the speed of the induced ionic effect can be drastically enhanced.

physics.app-ph↗

arXiv2021

Ion irradiation and implantation modifications of magneto-ionically induced exchange bias in Gd/NiCoO

Magneto-ionic control of magnetic properties through ionic migration has shown promise in enabling new functionalities in energy-efficient spintronic devices. In this work, we demonstrate the effect of helium ion irradiation and oxygen implantation on magneto-ionically induced exchange bias effect in Gd/Ni$_{0.33}$Co$_{0.67}$O heterostructures. Irradiation using $He^+$ leads to an expansion of the Ni$_{0.33}$Co$_{0.67}$O lattice due to strain relaxation. At low He+ fluence ($\leq$ 2$\times$10$^{14}$ ions cm$^{-2}$), the redox-induced interfacial magnetic moment initially increases, owing to enhanced oxygen migration. At higher fluence, the exchange bias is suppressed due to reduction of pinned uncompensated interfacial Ni$_{0.33}$Co$_{0.67}$O spins. For oxygen implanted samples, an initial lattice expansion below a dose of 5$\times$10$^{15}$ cm$^{-2}$ is subsequently dominated at higher dose by a lattice contraction and phase segregation into NiO and CoO-rich phases, which in turn alters the exchange bias. These results highlight the possibility of ion irradiation and implantation as an effective means to tailor magneto-ionic effects.

cond-mat.mtrl-sci↗

arXiv2021

Electrically Enhanced Exchange Bias via Solid State Magneto-Ionics

Electrically induced ionic motion offers a new way to realize voltage-controlled magnetism, opening the door to a new generation of logic, sensor, and data storage technologies. Here, we demonstrate an effective approach to magneto-ionically and electrically tune exchange bias in Gd/Ni$_{1-x}$Co$_{x}$O thin films (x=0.50, 0.67), where neither of the layers alone is ferromagnetic at room temperature. The Gd capping layer deposited onto antiferromagnetic Ni$_{1-x}$Co$_{x}$O initiates a solid-state redox reaction that reduces an interfacial region of the oxide to ferromagnetic NiCo. Exchange bias is established after field cooling, which can be enhanced by up to 35% after a voltage conditioning and subsequently reset with a second field cooling. These effects are caused by the presence of an interfacial ferromagnetic NiCo layer, which further alloys with the Gd layer upon field cooling and voltage application, as confirmed by electron microscopy and polarized neutron reflectometry studies. These results highlight the viability of the solid-state magneto-ionic approach to achieve electric control of exchange bias, with potentials for energy-efficient magneto-ionic devices.

cond-mat.mtrl-sci↗

arXiv2021

Efficient and Robust Metallic Nanowire Foams for Deep Submicrometer Particulate Filtration

The on-going COVID-19 pandemic highlights the severe health risks posed by deep submicron sized airborne viruses and particulates in the spread of infectious diseases. There is an urgent need for the development of efficient, durable and reusable filters for this size range. Here we report the realization of efficient particulate filters using nanowire-based low-density metal foams which combine extremely large surface areas with excellent mechanical properties. The metal foams exhibit outstanding filtration efficiencies (>96.6%) in the PM_{0.3} regime, with potentials for further improvement. Their mechanical stability and light weight, chemical and radiation resistance, ease of cleaning and reuse, and recyclability further make such metal foams promising filters for combating COVID-19 and other types of airborne particulates.

cond-mat.mtrl-sci↗

arXiv2020

Systematic Characterization of Hydrophilized Polydimethylsiloxane

Flexible microfluidics have found extensive utility in the biological and biomedical fields. A leading substrate material for compliant devices is polydimethylsiloxane (PDMS). Despite its many advantages, PDMS is inherently hydrophobic and consequently its use in passive (pumpless) microfluidics becomes problematic. To this end, many physical and chemical modifications have been introduced to render PDMS hydrophilic, ranging from amphiphilic molecule additions to surface plasma treatments. However, when transitioning from lab benchtop to realized medical devices, these modifications must exhibit long-term stability. Unfortunately, these modifications are often presented but their mechanisms and long-term stability are not studied in detail. We have investigated an array of PDMS modifications, utilizing contact angle goniometry to study surface energy over a 30-day evolution study. Samples were stored in air and water, and Fourier Transform Infrared-Attenuated Total Reflectance (FTIR-ATR) analysis was used to confirm surface functional group uniformity. We have identified preferred modification techniques for long-lasting PDMS devices and characterized often overlooked material stability.

physics.app-ph↗

arXiv2020

Reversible and magnetically unassisted voltage-driven switching of magnetization in FeRh/PMN-PT

Reversible control of magnetization by electric fields without assistance from a subsidiary magnetic field or electric current could help reduce the power consumption in spintronic devices. When increasing temperature above room temperature, FeRh displays an uncommon antiferromagnetic to ferromagnetic phase transition linked to a unit cell volume expansion. Thus, using the strain exerted by an adjacent piezoelectric layer, the relative amount of antiferromagnetic and ferromagnetic regions can be tuned by an electric field applied to the piezoelectric material. Indeed, large variations in the saturation magnetization have been observed when straining FeRh films grown on suitable piezoelectric substrates. In view of its applications, the variations in the remanent magnetization rather than those of the saturation magnetization are the most relevant. Here, we show that in the absence of any bias external magnetic field, permanent and reversible magnetization changes as high as 34% can be induced by an electric field, which remain after this has been zeroed. Bulk and local magnetoelectric characterization reveals that the fundamental reason for the large magnetoelectric response observed at remanence is the expansion (rather than the nucleation) of ferromagnetic nanoregions.

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↗