arXiv subjects

Yoav Kalcheim

Publications and source records attributed to Yoav Kalcheim.

At least 19 recordsLinked to original sources

arXiv2026

Electrical Control over Volatile Mott Switching through Non-Volatile Memory Effects

Vanadium Dioxide (VO2) and Vanadium Sesquioxide (V2O3) are Mott insulators that undergo an Insulator-to-Metal Transition (IMT) at ~340K and ~160K, respectively, manifested as an orders-of-magnitude reduction in their electrical resistance. These transitions provide the physical basis for their Volatile Resistive Switching (VRS) behavior, making them promising candidates for threshold-switching devices. Here, we show that the volatile switching in these materials can be strongly affected by non-volatile processes associated with the creation and annihilation of the conducting filament. These processes give rise to pronounced memory effects in which the initial switching voltage substantially exceeds that of subsequent cycles. We identify two distinct mechanisms underlying this behavior in different thermal regimes. In the phase-coexistence regime, a memory effect is observed in V2O3, arising from the spatial redistribution of metallic and insulating domains. Well below the hysteresis regime, an additional electroforming-like memory effect is observed in both VO2 and V2O3 which is attributed to the formation and/or migration of defects under the influence of a high electric field and a current surge associated with the IMT-driven switching. Using a protective internal resistor and a multi-step writing protocol, this normally destructive process can be harnessed to tune the switching voltage and power over a wide temperature range. These results demonstrate a route toward controlled programming of switching parameters in IMT-based resistive switching devices.

cond-mat.mtrl-sci↗

arXiv2026

Harnessing the VO2 Phase Transition for Automatic Gain Control in Transimpedance Amplifiers

Transimpedance amplifiers (TIAs) are essential in sensor electronics, converting input currents into output voltages. Conventional TIAs utilize fixed-gain resistors, which saturate under high input currents and consequently result in undesirable recovery times. To overcome this limitation, volatile resistive switching devices have emerged as a promising alternative, offering intrinsic automatic gain control (AGC). Among these, vanadium dioxide (VO2) devices stand out for their reversible insulator-metal transition (IMT), producing abrupt, energy-efficient resistance changes near the transition temperature (67 C). In this work, a switching device was fabricated by sputtering a VO2 thin film and patterning 200 nm electrode gaps atop it. Before integrating this device into the TIA circuit, its switching dynamics were characterized under electrical pulse excitation. Slightly exceeding the temperature-dependent IMT threshold voltage (Vth) yielded fast and reproducible switching. Complementary pump-probe measurements showed that operating well below TC effectively suppresses short-term memory effects linked to the stochastic nature of the first-order transition. Leveraging these insights, a custom VO2-based TIA was developed, demonstrating variable gain and AGC functionality. Furthermore, applying a constant DC current bias during switching induced self-sustained oscillations (2 pJ per spike) with frequencies up to 60 MHz, consistent with the thermal timescale of the VO2 devices. Overall, these results provide a detailed understanding of VO2 switching dynamics and demonstrate their potential for enabling compact, energy-efficient AGC in high-speed TIAs for advanced sensing applications.

cond-mat.str-el↗

arXiv2026

Martensitic laminate geometry controls electronic phase transitions in a Mott insulator

Symmetry-lowering structural phase transitions result in multiple degenerate structures whose coexistence is determined by macroscopic strain compatibility. In quantum materials, these structural transformations often couple to electronic degrees of freedom, yet how the structural arrangements influence electronic phase transitions remains poorly understood. By analyzing hundreds of diffraction peaks from X-ray reciprocal space mapping, we determine the lattice basis vectors and mutual orientations of all coexisting phases in epitaxial V2O3 thin films after a symmetry-lowering transformation coincident with a metal-insulator transition. We identify the orientations of interfaces between all coexisting structures using the theory of martensitic phase transformations and find that the low temperature structure comprises finely tuned layered mixtures of alternating twin variants, akin to metal alloys. By comparing films grown on various substrate orientations, we show that the metal-insulator transition temperature increases monotonically with the degree to which these layered mixtures satisfy macroscopic strain compatibility imposed by the substrate.

cond-mat.mtrl-sci↗

arXiv2025

Reversal of strain state in a Mott insulator thin film by controlling substrate morphology

The V2O3 phase diagram contains two insulating phases and one metallic phase with different lattice structures. The stability of these phases is very sensitive to pressure, offering a mechanism to tune phase transitions by inducing strain in thin films. The most studied source of strain is lattice mismatch between the film and the substrate. In this work, however, we find that the film/substrate thermal expansion mismatch can be made to play a dominant role by modifying the substrate morphology. When grown on sapphire, the lattice mismatch induces compressive strain in the V2O3 films, whereas thermal expansion mismatch induces tensile strain. We find that minute changes in substrate morphology may relax the compressive strain component, allowing the thermally-induced tensile component to overcome it. Thus, by simple annealing of the substrates to create either a flat or stepped morphology, strongly compressive or tensile strains may be induced in the films. This results in either full suppression of the metal-insulator transition or stabilization of insulating phases at all temperatures, exhibiting many orders of magnitude differences in film resistivity. To elucidate the strain relaxation mechanism, we use high-resolution scanning transmission electron microscopy (HRSTEM) to image the atomic steps in the substrate and the adjacent crystallographic defects in the V2O3. These findings offer a hitherto underexplored mechanism to tune strain in thin films, deepen our understanding of the effects of structural degrees of freedom on phase stability of a canonical Mott insulator and may allow for applications requiring insulator-metal switching above room temperature.

cond-mat.mtrl-sci↗

arXiv2025

Disentangling pre-transitional fluctuations in metallic VO2

VO2 features concomitant structural and metal-insulator transitions. This poses a challenge for understanding the underlying mechanism: is the transition triggered by a structural or by an electronic instability? The two scenarios are expected to produce very different pre-transitional fluctuations above TC. By combining magnetic susceptibility, IR reflectivity and X-ray diffuse scattering measurements, we observe that metallic VO2 features strong electronic and structural fluctuations towards the insulating monoclinic phase. By measuring resonant diffuse X-ray scattering across the Vanadium K-edge, we search for a potential decoupling between electronic and structural ordering in these fluctuations, finding no evidence of it. While our results do not completely rule out pure electronic fluctuations, they constrain them, favoring the interpretation that the VO2 metal-insulator transition is triggered by a structural instability. Our work offers a novel approach to solve similar problems in other strongly correlated systems.

cond-mat.str-el↗

arXiv2024

Magnetic precursor to the structural phase transition in V$_2$O$_3$

The coupling between structural, electronic and magnetic degrees of freedom across the metal-insulator transition in V2O3 makes it hard to determine the main driving mechanism behind the transition. Specifically, the role of magnetism has been debated and its interplay with the other transitions has not been established. To address this issue, we use a combination of muon spin relaxation/rotation, electrical transport and reciprocal space mapping which allows to correlate magnetic, electronic and structural degrees of freedom in strain-engineered V2O3 thin films. Evidence is found for a magnetic instability in the vicinity of the structural transition. This is manifested as a decrease in the antiferromagnetic moment with temperature leading to a virtual N\'eel transition temperature which coincides with that of the structural and electronic transitions. Moreover, we find evidence for an onset of antiferromagnetic (AF) fluctuations in the rhombohedral phase even without a structural transition to the monoclinic phase. The non-congruence of the structural and magnetic transitions increases as the transition temperature is reduced by strain. In samples where the transition is most strongly suppressed by strain, a depth-dependent magnetic state is observed. These results reveal the importance of an AF instability in the paramagnetic phase in triggering the metal-insulator transition and the crucial role of the structural transition in allowing for the formation of an ordered AF state.

cond-mat.str-el↗

arXiv2024

X-ray Nano-imaging of a Heterogeneous Structural Phase Transition in V2O3

Controlling the Mott transition through strain engineering is crucial for advancing the development and application of memristive and neuromorphic computing devices. Yet, Mott insulators are heterogeneous due to intrinsic phase boundaries and extrinsic defects, posing significant challenges to fully understanding the impact of local microscopic distortions on the local Mott transition. Addressing these challenges demands structural characterizations at the relevant length scale. Here, using a synchrotron-based scanning X-ray nanoprobe, we studied the real-space structural heterogeneity during the structural phase transition in a V2O3 thin film. Through temperature-dependent metal-insulator phase coexistence mapping, we report a variation in the local transition temperature of up to 7 K across the film and the presence of the transition hysteresis at the nanoscale. Furthermore, a detailed quantitative analysis demonstrates that the spatial heterogeneity of the transition is closely tied to the tilting of crystallographic planes in the pure insulating phase. Our work highlights the impact of local heterogeneity on the Mott transition and lays the groundwork for future innovations in harnessing strain heterogeneity within Mott systems for the next-generation computational technologies.

cond-mat.mtrl-sci↗

arXiv2024

Electric field induced resistive switching in M$^{3+}_x$V$_{1-x}$O$_2$ (M$^{3+}$= Ga$^{3+}$, Al$^{3+}$) single crystals at temperatures below the T $\to$ M2 phase transition

The phase diagram of VO$_2$ strained or doped with several trivalent ions consists of four phases; in order of increasing temperatures, three (M1, T and M2) are insulating while the fourth (R), above ~340 K, is metallic. These phases and the three phase transitions have been thoroughly investigated for about half a century by a wide variety of techniques, including electronic transport. While an upwards jump of the resistance of up to a factor of 2 was observed at the T-M2 transition and a drop of several orders of magnitude was observed at the M2$\to$R one, resistive switching at the M1$\to$T transition remained elusive over all these years. Here we report on the investigation of Ga- and Al-doped VO$_2$ single crystals, following the rather surprising appearance of a small and steep drop of a factor of ~ 0.12 in the resistance of Ga-doped VO$_2$ single crystals detected by pulsed and DC I-V measurements carried out at room temperature, below the T$\to$M2 phase transition. Similar results were obtained also from measurements on Al-doped VO2 single crystals. Raman spectra of Ga-, and Al-doped crystals resolved their structures as function of temperature. The accumulated results of the measurements on Ga-, and Al-doped single crystals provide evidence for identifying the resistive switching at T$_{\rm RS}$<T$_{\rm T\to M2}$ with the M1$\to$T transition.

cond-mat.str-el↗

arXiv2024

Laser-induced quenching of metastability at the Mott-insulator to metal transition

There is growing interest in strongly correlated insulator thin films because the intricate interplay of their intrinsic and extrinsic state variables causes memristive behavior that might be used for bio-mimetic devices in the emerging field of neuromorphic computing. In this study we find that laser irradiation tends to drive V$_2$O$_3$ from supercooled/superheated metastable states towards thermodynamic equilibrium, most likely in a non-thermal way. We study thin films of the prototypical Mott-insulator V$_2$O$_3$, which show spontaneous phase separation into metal-insulator herringbone domains during the Mott transition. Here, we use low-temperature microscopy to investigate how these metal-insulator domains can be modified by scanning a focused laser beam across the thin film surface. We find that the response depends on the thermal history: When the thin film is heated from below the Mott transition temperature, the laser beam predominantly induces metallic domains. On the contrary, when the thin film is cooled from a temperature above the transition, the laser beam predominantly induces insulating domains. Very likely, the V$_2$O$_3$ thin film is in a superheated or supercooled state, respectively, during the first-order phase transition, and the perturbation by a laser beam drives these metastable states into stable ones. This way, the thermal history is locally erased. Our findings are supported by a phenomenological model with a laser-induced lowering of the energy barrier between the metastable and equilibrium states.

cond-mat.str-el↗

arXiv2023

Coupled pyroelectric-photovoltaic effect in 2D ferroelectric $\alpha$-In$_2$Se$_3$

Pyroelectric and photovoltaic effects are vital in cutting-edge thermal imaging, infrared sensors, thermal and solar energy harvesting. Recent advances revealed the great potential of the bulk photovoltaic effect in two-dimensional (2D) semiconductor-ferroelectric materials to enable reconfigurable p-n junction operation with the potential to surpass the Shockley-Queiseer limit. Moreover, the extremely low thickness, high thermal conductivity, dangling bonds free interface, and room-temperature stable ferroelectricity down to a single monolayer endow 2D ferroelectrics with a superior pyroelectric figure of merit. Herein, we performed direct pyroelectric measurements of 2D $\alpha$-In$_2$Se$_3$ under dark and light conditions. The results reveal a gigantic pyroelectric coefficient of 30.7 mC/m$^2$K and a figure of merit of 135.9 m$^2$/C. In addition, we perform temperature-dependent short-circuit photovoltaic response measurements in which the excess photocurrent is modulated in proportion with the temperature variations due to the induced in-plane potential variations. Consequently, the discovered pyroelectric-photovoltaic effect allows the combination of direct temperature (photovoltaic) and temperature-derivative (pyroelectric) sensing. Finally, we utilized the intercoupled ferroelectricity of In$_2$Se$_3$ to realize a non-volatile, self-powered photovoltaic memory operation, demonstrating a stable short-circuit current switching with a decent 103 ON-OFF ratio. The coupled pyroelectric-photovoltaic effect, along with reconfigurable photocurrent, pave the way for a novel monolithic device technology with integrated thermal and optical response, in-memory logic and energy harvesting.

physics.app-ph↗

arXiv2023

Domain nucleation across the metal-insulator transition of self-strained V2O3 films

Bulk V2O3 features concomitant metal-insulator (MIT) and structural (SPT) phase transitions at TC ~ 160 K. In thin films, where the substrate clamping can impose geometrical restrictions on the SPT, the epitaxial relation between the V2O3 film and substrate can have a profound effect on the MIT. Here we present a detailed characterization of domain nucleation and growth across the MIT in (001)-oriented V2O3 films grown on sapphire. By combining scanning electron transmission microscopy (STEM) and photoelectron emission microscopy (PEEM), we imaged the MIT with planar and vertical resolution. We observed that upon cooling, insulating domains nucleate at the top of the film, where strain is lowest, and expand downwards and laterally. This growth is arrested at a critical thickness of 50 nm from the substrate interface, leaving a persistent bottom metallic layer. As a result, the MIT cannot take place in the interior of films below this critical thickness. However, PEEM measurements revealed that insulating domains can still form on a very thin superficial layer at the top interface. Our results demonstrate the intricate spatial complexity of the MIT in clamped V2O3, especially the strain-induced large variations along the c-axis. Engineering the thickness-dependent MIT can provide an unconventional way to build out-of-plane geometry devices by using the persistent bottom metal layer as a native electrode.

cond-mat.mtrl-sci↗

arXiv2023

Anomalous T-dependence of phonon lifetimes in metallic VO2

We investigate phonon lifetimes in VO2 single crystals. We do so in the metallic state above the metal-insulator transition (MIT), where strong structural fluctuations are known to take place. By combining inelastic X-ray scattering and Raman spectroscopy, we track the temperature dependence of several acoustic and optical phonon modes up to 1000 K. Contrary to what is commonly observed, we find that phonon lifetimes decrease with decreasing temperature. Our results show that pre-transitional fluctuations in the metallic state give rise to strong electron-phonon scattering that onsets hundreds of degrees above the transition and increases as the MIT is approached. Notably, this effect is not limited to specific points of reciprocal space that could be associated with the structural transition.

cond-mat.str-el↗

arXiv2022

Imaging the itinerant-to-localized transmutation of electrons across the metal-to-insulator transition in V$_2$O$_3$

In solids, strong repulsion between electrons can inhibit their movement and result in a "Mott" metal-to-insulator transition (MIT), a fundamental phenomenon whose understanding has remained a challenge for over 50 years. A key issue is how the wave-like itinerant electrons change into a localized-like state due to increased interactions. However, observing the MIT in terms of the energy- and momentum-resolved electronic structure of the system, the only direct way to probe both itinerant and localized states, has been elusive. Here we show, using angle-resolved photoemission spectroscopy (ARPES), that in V$_2$O$_3$ the temperature-induced MIT is characterized by the progressive disappearance of its itinerant conduction band, without any change in its energy-momentum dispersion, and the simultaneous shift to larger binding energies of a quasi-localized state initially located near the Fermi level.

cond-mat.str-el↗

arXiv2022

Direct visualization of percolating metal-insulator transition in V2O3 using scanning microwave impedance microscopy

Using the extensively studied V2O3 as a prototype system, we investigate the role of percolation in metal-insulator transition (MIT). We apply scanning microwave impedance microscopy to directly determine the metallic phase fraction p and relate it to the macroscopic conductance G, which shows a sudden jump when p reaches the percolation threshold. Interestingly, the conductance G exhibits a hysteretic behavior against p, suggesting two different percolating processes upon cooling and warming. Based on our image analysis and model simulation, we ascribe such hysteretic behavior to different domain nucleation and growth processes between cooling and warming, which is likely caused by the decoupled structural and electronic transitions in V2O3 during MIT. Our work provides a microscopic view of how the interplay of structural and electronic degrees of freedom affects MIT in strongly correlated systems.

cond-mat.str-el↗

arXiv2021

Uniform structural phase transition in V$_2$O$_3$ without short-range distortions of the local structure

The local structure of V$_{2}$O$_{3}$, an archetypal strongly correlated electron system that displays a metal-insulator transition around 160 K, has been investigated via pair distribution function (PDF) analysis of neutron and x-ray total scattering data. The rhombohedral-to-monoclinic structural phase transition manifests as an abrupt change on all length scales in the observed PDF. No monoclinic distortions of the local structure are found above the transition, although coexisting regions of phase-separated rhombohedral and monoclinic symmetry are observed between 150 K and 160 K. This lack of structural fluctuations above the transition contrasts with the known presence of magnetic fluctuations in the high-temperature state, suggesting that the lattice degree of freedom plays a secondary role behind the spin degree of freedom in the transition mechanism.

cond-mat.str-el↗

arXiv2020

Direct observation of the electrically triggered Insulator-Metal transition in V3O5 far below the transition temperature

Resistive switching is one of the key phenomena for applications such as nonvolatile memories or neuromorphic computing. V3O5, a compound of the vanadium oxide Magn\'eli series, is one of the rare materials to exhibit an insulator-metal transition (IMT) above room temperature (Tc ~ 415 K). Here we demonstrate both static dc resistive switching (RS) and fast oscillatory spiking regimes in V3O5 devices at room temperature (120 K below the phase transition temperature) by applying an electric field. We use operando optical imaging to track a reflectivity change during the RS and find that a percolating high temperature metallic phase filament is formed. This demonstrates that the electrically induced RS triggers the phase transition. Furthermore, we optically capture the spiking oscillations that we link to the negative differential resistance regime and find the filament forms and dissolves via a periodic spatio-temporal instability that we describe by numerical simulations.

cond-mat.mtrl-sci↗

arXiv2020

A hybrid optoelectronic Mott insulator

The coupling of electronic degrees of freedom in materials to create hybridized functionalities is a holy grail of modern condensed matter physics that may produce novel mechanisms of control. Correlated electron systems often exhibit coupled degrees of freedom with a high degree of tunability which sometimes lead to hybridized functionalities based on external stimuli. However, the mechanisms of tunability and the sensitivity to external stimuli are determined by intrinsic material properties which are not always controllable. A Mott metal-insulator transition, which is technologically attractive due to the large changes in resistance, can be tuned by doping, strain, electric fields, and orbital occupancy but cannot be, in and of itself, controlled externally with light. Here we present a new approach to produce hybridized functionalities using a properly engineered photoconductor/strongly-correlated hybrid heterostructure, showing control of the Metal-to-Insulator transition (MIT) using optical means. This approach combines a photoconductor, which does not exhibit an MIT, with a strongly correlated oxide, which is not photoconducting. Due to the close proximity between the two materials, the heterostructure exhibits large volatile and nonvolatile, photoinduced resistivity changes and substantial photoinduced shifts in the MIT transition temperatures. This approach can potentially be extended to other judiciously chosen combinations of strongly correlated materials with systems which exhibit optically, electrically or magnetically controllable behavior.

physics.app-ph↗

arXiv2020

Optical imaging of strain-mediated phase coexistence during electrothermal switching in a Mott insulator

Resistive-switching -- the current-/voltage-induced electrical resistance change -- is at the core of memristive devices, which play an essential role in the emerging field of neuromorphic computing. This study is about resistive switching in a Mott-insulator, which undergoes a thermally driven metal-to-insulator transition. Two distinct switching mechanisms were reported for such a system: electric-field-driven resistive switching and electrothermal resistive switching. The latter results from an instability caused by Joule heating. Here, we present the visualization of the reversible resistive switching in a planar V$_2$O$_3$ thin-film device using high-resolution wide-field microscopy in combination with electric transport measurements. We investigate the interaction of the electrothermal instability with the strain-induced spontaneous phase-separation in the V$_2$O$_3$ thin film at the Mott-transition. The photomicrographs show the formation of a narrow metallic filament with a minimum width $\lesssim$ 500\,nm. Although the filament formation and the overall shape of the current-voltage characteristics (IVCs) are typical of an electrothermal breakdown, we also observe atypical effects like oblique filaments, filament splitting, and hysteretic IVCs with sawtooth-like jumps at high currents in the low-resistance regime. We were able to reproduce the experimental results in a numerical model based on a two-dimensional resistor network. This model demonstrates that resistive switching, in this case, is indeed electrothermal and that the intrinsic heterogeneity is responsible for the atypical effects. This heterogeneity is strongly influenced by strain, thereby establishing a link between switching dynamics and structural properties.

cond-mat.mtrl-sci↗