Temperature-dependent Measurements Research Articles

Structural behavior and electrical transport properties of Mg2Ge under high pressure

The structural and electrical transport properties are investigated from ambient pressure to 40 GPa for Mg2Ge using first-principles calculations and in situ high-pressure electrical experiments. Mg2Ge undergoes reversible phase transitions from anti-fluorite structure to anti-cotunnite structure and then to Ni2In-type structure by enthalpy calculations, both reflected in the cell volume collapse and discontinuous axial ratios of lattice constants. The inter- and intra-layer sliding of Mg and Ge atomic pairs is revealed induced by phase transitions. The metallization transition is determined by the energy-band closure, in good agreement with the enhancing metallic behavior experimentally evidenced above approximately 7 GPa according to the temperature-dependent resistivity measurement. The structural phase transitions are determined at around 9.6 GPa and 35.8 GPa based on discontinuous electrical parameters. The paper tends to shed light on the structural behaviors and electrical transport properties of intermetallic compounds Mg2X-type (X = IVA group elements) family under extreme conditions.

Optically Tunable Electrical Oscillations in Oxide-Based Memristors for Neuromorphic Computing.

The application of hardware-based neural networks can be enhanced by integrating sensory neurons and synapses that enable direct input from external stimuli. This work reports direct optical control of an oscillatory neuron based on volatile threshold switching in V3O5. The devices exhibit electroforming-free operation with switching parameters that can be tuned by optical illumination. Using temperature-dependent electrical measurements, conductive atomic force microscopy (C-AFM), in situ thermal imaging, and lumped element modelling, it is shown that the changes in switching parameters, including threshold and hold voltages, arise from overall conductivity increase of the oxide film due to the contribution of both photoconductive and bolometric characteristics of V3O5, which eventually affects the oscillation dynamics. Furthermore, V3O5 is identified as a new bolometric material with a temperature coefficient of resistance (TCR) as high as -4.6% K-1 at 423 K. The utility of these devicesis illustrated by demonstrating in-sensor reservoir computing with reduced computational effort and an optical encoding layer for spiking neural network (SNN), respectively, using a simulated array of devices.

Enabling High Activation of Glucose-6-Phosphate Dehydrogenase Activity Through Liquid Condensate Formation and Compression.

Droplet formation via liquid-liquid phase separation is thought to be involved in the regulation of various biological processes, including enzymatic reactions. We investigated a glycolytic enzymatic reaction, the conversion of glucose-6-phosphate to 6-phospho-D-glucono-1,5-lactone with concomitant reduction of NADP+ to NADPH both in the absence and presence of dynamically controlled liquid droplet formation. Here, the nucleotide serves as substrate as well as the scaffold required for the formation of liquid droplets. To further expand the process parameter space, temperature and pressure dependent measurements were performed. Incorporation of the reactants in the liquid droplet phase led to a boost in enzymatic activity, which was most pronounced at medium-high pressures. The crowded environment of the droplet phase induced a marked increase of the affinity of the enzyme and substrate. An increase in turnover number in the droplet phase at high pressure contributed to a further strong increase in catalytic efficiency. Enzyme systems that are dynamically coupled to liquid condensate formation may be the key to deciphering many biochemical reactions. Expanding the process parameter space by adjusting temperature and pressure conditions can be a means to further increase the efficiency of industrial enzyme utilization and help uncover regulatory mechanisms adopted by extremophiles.

Electron paramagnetic resonance as a tool to determine the sodium charge storage mechanism of hard carbon

Hard carbon is a promising negative electrode material for rechargeable sodium-ion batteries due to the ready availability of their precursors and high reversible charge storage. The reaction mechanisms that drive the sodiation properties in hard carbons and subsequent electrochemical performance are strictly linked to the characteristic slope and plateau regions observed in the voltage profile of these materials. This work shows that electron paramagnetic resonance (EPR) spectroscopy is a powerful and fast diagnostic tool to predict the extent of the charge stored in the slope and plateau regions during galvanostatic tests in hard carbon materials. EPR lineshape simulation and temperature-dependent measurements help to separate the nature of the spins in mechanochemically modified hard carbon materials synthesised at different temperatures. This proves relationships between structure modification and electrochemical signatures in the galvanostatic curves to obtain information on their sodium storage mechanism. Furthermore, through ex situ EPR studies we study the evolution of these EPR signals at different states of charge to further elucidate the storage mechanisms in these carbons. Finally, we discuss the interrelationship between EPR spectroscopy data of the hard carbon samples studied and their corresponding charging storage mechanism.

Inhibition of amyloid fibrillation of single amino acid tryptophan by tannic acid: An insight into targeted therapy of hypertryptophanemia disorder

Amyloid fibrillation involving specific amino acids is a key factor contributing to the development of various neurodegenerative disorders, which remain being investigated. A promising therapeutic approach for treatment involves the use of small molecules to inhibit this amyloid fibrillation. In this study, we present experimental evidence demonstrating the efficacy of tannic acid (TA) as a potent inhibitor of fibrillation, particularly in the case of the single amino acid tryptophan (Trp), which is associated with hypertryptophanemia disorder. To investigate the kinetics of fibril formation and its suppression by TA, we have employed a combination of steady-state and time-resolved fluorescence measurements. These techniques have allowed us to monitor changes in the intrinsic fluorescence of Trp and an amyloid-specific fluorophore over time. To visualize the effects of TA on Trp fibrils, we have employed various imaging techniques such as, atomic force microscopy, transmission electron microscopy, and field emission scanning electron microscopy. These imaging techniques have vividly captured the TA-induced disruption of long Trp fibrils. Dynamic light scattering measurements have complemented these microscopic observations, further supporting the notion that TA effectively hinders the formation and stability of Trp fibrils. Additionally, we have determined the binding constant and calculated changes in the free energy associated with Trp-TA interactions through temperature-dependent spectroscopic measurements. These thermodynamic analyses provide valuable insights into the underlying mechanisms of TA-induced disaggregation of larger Trp fibrils.

Incidence of the Brownian Relaxation Process on the Magnetic Properties of Ferrofluids.

Ferrofluids containing magnetic nanoparticles represent a special class of magnetic materials due to the added freedom of particle tumbling in the fluids. We studied this process, known as Brownian relaxation, and its effect on the magnetic properties of ferrofluids with controlled magnetite nanoparticle sizes. For small nanoparticles (below 10 nm diameter), the Néel process is expected to dominate the magnetic response, whereas for larger particles, Brownian relaxation becomes important. Temperature- and magnetic-field-dependent magnetization studies, differential scanning calorimetry, and AC susceptibility measurements were carried out for 6 and 13.5 nm diameter magnetite nanoparticles suspended in water. We identify clear fingerprints of Brownian relaxation for the sample of large-diameter nanoparticles as both magnetic and thermal hysteresis develop at the water freezing temperature, whereas the samples of small-diameter nanoparticles remain hysteresis-free down to the magnetic blocking temperature. This is supported by the temperature-dependent AC susceptibility measurements: above 273 K, the data show a low-frequency Debye peak, which is characteristic of Brownian relaxation. This peak vanishes below 273 K.

Origin and Recovery of Negative VTH Shift on 4H–SiC MOS Capacitors: An Analysis Based on Inverse Laplace Transform and Temperature-Dependent Measurements

SiC power MOSFETs are reported to suffer from both positive and negative threshold voltage shifts. Positive shift is well understood in the literature and attributed to electron trapping in near interface oxide traps (NIOTs). Negative shift is explained by hole generation and trapping in the oxide via impact ionization favored by the strong oxide field. However, studies on negative shift are still ongoing, and the origin and nature of the process are not fully understood. This study advances the comprehension of negative threshold voltage shift by investigating MOS capacitors subject to positive bias stress.We demonstrate that: a) a significant negative threshold shift is observed when the electric field is greater than 7.5 MV/cm; b) the detected shift is not recoverable at zero bias. Recovery can be obtained only by applying a positive gate voltage indicating a field-driven detrapping process. c) Trap-state mapping measurements were carried out to extract the activation energy of the detrapping processes, and a weak thermal activation was observed.Results collected within this paper indicate that holes are trapped at deep centers, and thermal detrapping is not possible. Hole release is only possible when a high field is applied to the insulator, possibly due to the recombination between leaking electrons and trapped holes.

Exploring Cu-Doped Co3O4 Bifunctional Oxygen Electrocatalysts for Aqueous Zn-Air Batteries.

The efficiency of oxygen electrocatalysis is a key factor in diverse energy domain applications, including the performance of metal-air batteries, such as aqueous Zinc (Zn)-air batteries. We demonstrate here that the doping of cobalt oxide with optimal amounts of copper (abbreviated as Cu-doped Co3O4) results in a stable and efficient bifunctional electrocatalyst for oxygen reduction (ORR) and evolution (OER) reactions in aqueous Zn-air batteries. At high Cu-doping concentrations (≥5%), phase segregation occurs with the simultaneous presence of Co3O4 and copper oxide (CuO). At Cu-doping concentrations ≤5%, the Cu ion resides in the octahedral (Oh) site of Co3O4, as revealed by X-ray diffraction (XRD)/Raman spectroscopy investigations and molecular dynamics (MD) calculations. The residence of Cu@Oh sites leads to an increased concentration of surface Co3+-ions (at catalytically active planes) and oxygen vacancies, which is beneficial for the OER. Temperature-dependent magnetization measurements reveal favorable d-orbital configuration (high eg occupancy ≈ 1) and a low → high spin-state transition of the Co3+-ions, which are beneficial for the ORR in the alkaline medium. The influence of Cu-doping on the ORR activity of Co3O4 is additionally accounted in DFT calculations via interactions between solvent water molecules and oxygen vacancies. The application of the bifunctional Cu-doped (≤5%) Co3O4 electrocatalyst resulted in an aqueous Zn-air battery with promising power density (=84 mW/cm2), stable cyclability (over 210 cycles), and low charge/discharge overpotential (=0.92 V).

Piezoelectric and Pyroelectric Properties of Organic MDABCO-NH4Cl3 Perovskite for Flexible Energy Harvesting

This study describes the synthesis and characterization of the lead-free organic ferroelectric perovskite N-methyl-N’-diazabicyclo [2.2.2]octonium)-ammonium trichloride (MDABCO-NH4Cl3). The electrospinning technique was employed to obtain nanofibers embedded with this perovskite in a PVC polymer for hybrid fiber production. The dielectric, piezoelectric, and pyroelectric properties of these fibers were carefully examined. Based on measurements of the dielectric permittivity temperature and frequency dependence, together with the pyroelectric results, a transition from a high temperature paraelectric to a ferroelectric phase that persisted at room temperature was found to occur at 438 K. The measured pyroelectric coefficient yielded values as high as 290 μC K−1 m−2, which is in between the values reported for MDABCO-NH4I3 and the semiorganic ferroelectric triglycine sulfate (TGS). The hybrid nanofibers exhibited good morphological characteristics and demonstrated very good piezoelectric properties. Specifically, a piezoelectric coefficient of 42 pC/N was obtained when applying a periodical force of 3 N and a piezoelectric voltage coefficient of geff = 0.65 V mN−1. The performance of these fibers is on par with that of materials discussed in the existing literature for the fabrication of nano energy-harvesting generators. Importantly, the perovskite nanocrystals within the fibers are protected from degradation by the surrounding polymer, making them a promising environmentally friendly platform for flexible mechanical energy harvesting.

Manipulating the phase stability of a halide perovskite, CH3NH3PbI3 by high-pressure cycling

Methylammonium lead iodide perovskite, CH3NH3PbI3 (MAPbI3) is a highly promising photovoltaic material, whose structural and electronic properties are very sensitive to applied stresses. Here, we show that the phase stability of a MAPbI3 crystal can be controlled by structural defects and strains. We synthesized a single crystal of MAPbI3 and measured its electrical properties across two successive structural phase transitions under applied pressure up to 4–9 GPa under multiple high-pressure cycling. We revealed three types of effects of this high-pressure treatment. (i) An increasing the level of defects and strains in the crystal greatly delays the first reconstructive phase transition, conserving the ambient-pressure tetragonal phase up to a record pressure of ∼1.4 GPa, much higher compared to its typical stability range of up to 0.3–0.5 GPa only. (ii) A time exposure of the crystal at a fixed pressure corresponding to the beginning of the second phase transition to a “destabilized” structure eliminated some of defects and strains; it down-shifted the phase boundaries back. (iii) A recrystallization of the sample after pressure-induced amorphization enhanced its structural stability against amorphization upon subsequent pressurization cycle. We proposed that the most abundant defects and strains, which could appear in the pressure-cycled MAPbI3 crystals, were related to migration of iodine atoms from their regular sites to the MA interstices. Temperature-dependent photoluminescence measurements indicated that the sample recovered after the high-pressure cycling crystallized back into the initial tetragonal crystal structure. Whereas, its stability range expanded toward lower temperatures by 20 K and a band gap slightly increased, from 1.59 to 1.625 eV (at 290 K). Using this organic-inorganic perovskite as an example, we show how the phase stability of such materials can be manipulated by creation and elimination of structural defects and local strains.

Enhanced structural, optical and electrical properties of polycrystalline WO3 thin films achieved by aluminum nanosheets coating

Herein the effects of aluminum nanosheets on the structural, morphological, optical and electrical properties of tungsten oxide thin films are reported. Polycrystalline phase of the thermally evaporated WO3 was achieved by the pulsed laser welding technique. The polycrystalline films are then coated with Al nanosheets of thicknesses of 100 nm and 150 nm by the ion coating technique. It is observed that Al induces the domination of the hexagonal structure of WO3 over the tetragonal. Associated with the enhanced crystallinity the light absorption in the films increased by more than 60% and the energy band gap narrowed significantly. Namely the energy band gap of the as grown WO3 decreased from 3.15 eV to 2.85 eV and 2.59 eV as the Al layer thickness increased from 100 to 150 nm, respectively. It is also observed that crystalline films of WO3 exhibited lower electrical resistivity compared to films fabricated by other techniques. The temperature dependent electrical resistivity measurement was carried out in the temperature range of 310–420 K. It showed room temperature values of 2.5 ( Ω cm), 2.2 ( Ω cm) and 1.9 ( Ω cm) and impurity levels centered at 0.25 eV, 0.34 eV and 0.16 eV for uncoated and films coated with Al nanosheets of thicknesses of 100 nm and 150 nm, respectively. The enhanced crystallinity that is accompanied with narrower energy band gap and lower electrical resistivity values make crystalline WO3 films promising for optoelectronic applications.

Synthesis of lithium doped magnesium ferrites and their vibrational and magnetic properties: Correlation of experimental and density functional theory

Recently, there has been an increased focus on investigating the possible use of ferrite nanoparticles as magnetic memory devices. In this study, we report on the structural, microstructural, Raman, density functional theory and magnetic characteristics of Mg1-xLixFe2O4 (x = 0, 0.15, 0.3, 0.45, 0.5 and 0.75). Samples were synthesized by solution combustion synthesis method. Samples were subjected to characterize X-ray diffraction (XRD), Scanning electron microscopy (SEM) and Raman Spectra. XRD reveals that all synthesized samples show a single phase formation and unit cell volume, crystallite size varied with an increase in Lithium-ion concentration. SEM micrographs confirmed the porous nature increases with the rise of Li concentration. Particles are agglomeration and spherical type of nature was confirmed by TEM images. Further, Raman Spectra confirms the spinel cubic structure of MgFe2O4 nanoparticles belongs to the Fd3m space group. Despite the fact that the full unit cell has 56 atoms (Z = 8), the smallest Bravais cell consists of only 14 atoms (Z = 2). Consequently, in order to understand this effect, the electronic structure of pure and doped models was investigated through the Band Structure and Density of States (D.O.S.) profiles. First the crystalline structure of pure and Li-doped MgFe2O4 was analyzed based on the optimized lattice parameters and M − O (M = Mg, Li and Fe) bond distances. The band-gap was computed to be 2.54 eV being a direct transition between two points, in an excellent agreement with the experimental measurements. To investigate the temperature dependent magnetic properties, the M − H loops of Li doped MgFe2O4 nanoparticles traced at below and above room temperature over the applied magnetic field ±60 kOe. The M − H loops recorded at above and below room temperature demonstrated that the ferromagnetic nature of the sample. Further, the magnetic properties was investigated using temperature dependent FC and ZFC magnetization measurements. Above room temperature, the ZFC and FC curves show irreversibility and split at certain temperatures, as well as a broad maximum in ZFC curves at blocking temperature (TB). Saturation magnetization (Ms) values are higher at 15 K compared to 300 K, attributed to reduced thermal fluctuation. Our results suggest that synthesized materials are useful for room temperature magnetic memory device application.

Influence of Crystallization Kinetics and Flow Behavior on Structural Inhomogeneities in 3D-Printed Parts Made from Semi-Crystalline Polymers.

We report the results of a study focusing on the influence of crystallization kinetics and flow behavior on structural inhomogeneities in 3D-printed parts made from polyamide 12 (PA12) and poly(lactic acid) (PLA) by dynamic mechanical analysis (DMA), differential scanning calorimetry (DSC), fast scanning calorimetry (FSC), and wide-angle X-ray diffraction (WAXD). Temperature-dependent WAXD measurements on the neat PLA filament reveal that PLA forms a single orthorhombic α phase during slow cooling and subsequent 2nd heating. The PA12 filament shows a well pronounced polymorphism with a reversible solid-solid phase transition between the (pseudo)hexagonal γ phase near room temperature and the monoclinic α' phase above the Brill transition temperature TB = 140 °C. The influence of the print bed temperature Tb on structure formation, polymorphic state, and degree of crystallinity χc of the 3D-printed parts is investigated by height and depth-dependent WAXD scans and compared with that of 3D-printed single layers, used as a reference. It is found that the heat transferred from successive layers has a strong influence on the polymorphic state of PA12 since a superimposed mixture of γ and α phases is present in the 3D-printed parts. In the case of PLA, a single α phase is formed. The print bed temperature has, in comparison to PA12, a major influence on the degree of crystallinity χc and thus the homogeneity of the 3D-printed parts, especially close to the print bed. By comparing the obtained results from WAXD, DMA, DSC, and FSC measurements with relevant printing times, guidelines for 3D-printed parts with a homogeneous structure are derived.

Intertwined crystal structure, magnetic, and charge transport properties in mixed valent A-site ordered manganite NdBaMn2O6

In the present work, we report a correlation between crystal structure, magnetic, and electrical properties in an exotic magnetic compound, NdBaMn2O6 having ∼92% ordering between Nd and Ba, investigated using temperature-dependent synchrotron x-ray diffraction (XRD), dc magnetization and transport measurements. Temperature-dependent XRD data reveals that the compound undergoes various complex crystallographic phase transitions from high-temperature (T > 320 K) P4/mmm phase to intermediate (320 K – 280 K) Cmmm phase to a mixed (Cmmm and P21am) phase (280 K – 220 K) and to low-temperature P21am phase (T < 220 K). It is found that these crystallographic phase compositions play a crucial role in controlling its magnetic and transport properties. Temperature-dependent dc magnetization data show a sharp drop at the onset of mixed phase (Cmmm + P21am) at 280 K followed by a broad hump at ∼ 220 K where mixed phase to P21am transition occurs, thus indicating a correlation between the structural and magnetic properties. The dc magnetization in the mixed phase region is calculated by considering a superposition of the magnetic moments of Cmmm and P21am phases weighted by the fraction of each phase, which exactly follows the experimental magnetization data. Temperature variation of resistivity data shows a jump at ∼260 K, a temperature corresponding to 50–50% phase composition of Cmmm and P21am phases. The compound shows insulating behavior over a whole temperature range as confirmed from the resistivity data. Further, application of magnetic field causes a shift of magnetic and transport transition temperatures which may be due to the magnetic field induced structural transition in the system.

Coherent Oscillations in a SrRuO3/BiFeO3 Superlattice.

We investigated the ultrafast dynamics of a SrRuO3/BiFeO3 superlattice grown on a SrTiO3 substrate using a near infrared pump-probe technique at various temperatures. The superlattice exhibits a ferromagnetic order inherited from the SrRuO3 layer. The pump-induced changes in the reflectivity reveal periodic oscillations. We found that the oscillation frequency can be well explained by zone-folded acoustic phonon oscillations, whose dispersion depends on the sound velocity, density, and thickness within the supercell of each constituent layer. It is found that the observed oscillation frequency corresponds to the A1 mode, which suggests that oscillations are excited due to pump-induced expansion of the SrRuO3 layer that absorbs the pump photon. Temperature-dependent measurements reveal significant suppression of the oscillation amplitude in the ferromagnetic state. The suppressed amplitude is proportional to the square of the magnetization, M(T)2. This phenomenon can be attributed to a strong magnetostriction effect of SrRuO3 that suppresses lattice expansion upon pumping.

Electronic structure of superconducting VN(111) films

Vanadium nitride (VN) is a transition-metal nitride with remarkable properties that have prompted extensive experimental and theoretical investigations in recent years. However, there is a current paucity of experimental research investigating the temperature-dependent electronic structure of single-crystalline VN. In this study, high-quality VN(111) films were successfully synthesized on α\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\alpha$$\\end{document}-Al2\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$_2$$\\end{document}O3\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$_3$$\\end{document}(0001) substrates using magnetron sputtering. The crystal and electronic structures of the VN films were characterized by a combination of high-resolution X-ray diffraction, low-energy electron diffraction, resonant soft X-ray absorption spectroscopy, and ultraviolet photoelectron spectroscopy. The electrical transport measurements indicate that the superconducting critical temperature of the VN films is around 8.1 K. Intriguingly, the temperature-dependent photoelectron spectroscopy measurements demonstrate a weak temperature dependence in the electronic structure of the VN films, which is significant for understanding the ground state of VN compounds.

Space-Confined Growth of Ultrathin P-Type GeTe Nanosheets for Broadband Photodetectors.

As p-type phase-change degenerate semiconductors, crystalline and amorphous germanium telluride (GeTe) exhibit metallic and semiconducting properties, respectively. However, the massive structural defects and strong interface scattering in amorphous GeTe films significantly reduce their performance. In this work, two-dimensional (2D) p-type GeTe nanosheets are synthesized via a specially designed space-confined chemical vapor deposition (CVD) method, with the thickness of the GeTe nanosheets reduced to 1.9nm. The space-confined CVD method improves the crystallinity of ultrathin GeTe by lowering the partial pressure of the reactant gas, resulting in GeTe nanosheets with excellent p-type semiconductor properties, such as a satisfactory on/off ratio of 105. Temperature-dependent electrical measurements demonstrate that variable-range hopping and optical-phonon-assisted hopping mechanisms dominate transport behavior at low and high temperatures, respectively. GeTe devices exhibit significantly high responsivity (6589 and 2.2 A W-1 at 633 and 980nm, respectively) and detectivity (1.67 × 1011 and 1.3 × 108 Jones at 633 and 980nm, respectively), making them feasible for broadband photodetectors in the visible to near-infrared range. Furthermore, the fabricated GeTe/WS2 diode exhibits a rectification ratio of 103 at zero gate voltage. These satisfactory p-type semiconductor properties demonstrate that ultrathin GeTe exhibits enormous potential for applications in optoelectronic interconnection circuits.

Drift of Schottky Barrier Height in Phase Change Materials.

Phase-change memory (PCM) devices have great potential as multilevel memory cells and artificial synapses for neuromorphic computing hardware. However, their practical use is hampered by resistance drift, a phenomenon commonly attributed to structural relaxation or electronic mechanisms primarily in the context of bulk effects. In this study, we reevaluate the electrical manifestation of resistance drift in sub-100 nm Ge2Sb2Te5 (GST) PCM devices, focusing on the contributions of bulk vs interface effects. We employ a combination of measurement techniques to elucidate the current transport mechanism and the electrical manifestation of resistance drift. Our steady-state temperature-dependent measurements reveal that resistance in these devices is predominantly influenced by their electrical contacts, with conduction occurring through thermionic emission (Schottky) at the contacts. Additionally, temporal current-voltage characterization allows us to link the resistance drift to a time-dependent increase in the Schottky barrier height. These findings provide valuable insights, pinpointing the primary contributor to resistance drift in PCM devices: the Schottky barrier height for hole injection at the interface. This underscores the significance of contacts (interface) in the electrical manifestation of drift in PCM devices.

Orbital Magneto-Nonlinear Anomalous Hall Effect in Kagome Magnet Fe_{3}Sn_{2}.

It has been theoretically predicted that perturbation of the Berry curvature by electromagnetic fields gives rise to intrinsic nonlinear anomalous Hall effects that are independent of scattering. Two types of nonlinear anomalous Hall effects are expected. The electric nonlinear Hall effect has recently begun to receive attention, while very few studies are concerned with the magneto-nonlinear Hall effect. Here, we combine experiment and first-principles calculations to show that the kagome ferromagnet Fe_{3}Sn_{2} displays such a magneto-nonlinear Hall effect. By systematic field angular and temperature-dependent transport measurements, we unambiguously identify a large anomalous Hall current that is linear in both applied in-plane electric and magnetic fields, utilizing a unique in-plane configuration. We clarify its dominant orbital origin and connect it to the magneto-nonlinear Hall effect. The effect is governed by the intrinsic quantum geometric properties of Bloch electrons. Our results demonstrate the significance of the quantum geometry of electron wave functions from the orbital degree of freedom and open up a new direction in Hall transport effects.

Ag-CsPbI3 nanocomposite structure in glasses boosts photoluminescence for efficient light emitting diodes

Nanocomposite structures based on perovskite nanocrystals (NCs) and metal nanostructures within transparent monolithic media hold promise for a wide range of applications in optoelectronics. However, the microstructure of such nanocomposites and the reason for enhanced emissions remain incompletely understood. In this work, we present the successful creation of Ag-CsPbI3 nanocomposite within a highly transparent borosilicate glass (Ag-CsPbI3 NCs@glass). We reveal that Ag and CsPbI3 NCs form after thermal treatment of the glass, either in the form of Ag-CsPbI3 heterostructures or of separate Ag and CsPbI3 NCs. Based on combined characterization of Mott-Schottky and steady-state photoluminescence (PL) of the products, we attribute the enhanced PL in the nanocomposite of Ag-CsPbI3 to the regulation of CsPbI3 lattice by Ag ions and/or the plasmonic effect of Ag NCs. Temperature-dependent time-resolved PL decay measurements suggest that Ag NCs could play an important role in the relaxation process of excited carriers by increasing the radiative recombination. Moreover, the Ag-CsPbI3 nanocomposite structure within the glass matrix curtails PL quenching caused by water molecules and high temperature. Using the Ag-CsPbI3 nanocomposite, we achieve high-performance white light-emitting diodes with a color rendering index of 83.9 and luminous efficiency of 58.07 lmW−1. This work elucidates the underlying mechanism on the enhanced PL in nanocomposites containing perovskite NCs and metal nanostructures, and aids in the rational design of glass-based perovskite nanocomposites for a diversity of optoelectronic applications.