Redistribution Of Ions Research Articles

Charge Carrier Dynamics at the Perovskite Interface with Self-Assembled Monolayers.

Self-assembled monolayers (SAMs) deposited on the hole-collecting electrodes of p-i-n perovskite solar cells effectively replace bulky hole transporting layers. However, the mechanism by which monolayers control the electronic processes and how they depend on the properties of the monolayer molecules remain poorly understood. In this study, we developed a simplified perovskite solar cell imitator with blocked electron extraction to investigate the photocurrent dynamics between the perovskite and the hole-collecting ITO electrode. We investigated the photoluminescence and photovoltage dynamics under short laser pulse excitation and addressed the influence of bulky and monomolecular hole transport layers. Our findings reveal that the photovoltage dynamics is significantly affected by the properties of the transport and perovskite layers, which in turn depend on the methods of sample preparation and exploration. Photocurrent dynamics is determined by several processes, including charge carrier displacement in the local electric field, hole transport to ITO, trapping of holes in interface trap states, and electron-hole recombination at the interface. We propose a model that takes into account molecular dipole moments and their ionization potentials to partially explain the different influences of different monolayers on the hole extraction and interfacial recombination rates. Additionally, the photovoltage dynamics also strongly depends on the illumination of the sample and shows memory effects that persist over minutes and hours and are attributed to the redistribution of ions.

Prolonged Hyperactivity Elicits Massive and Persistent Chloride Ion Redistribution in Subsets of Cultured Hippocampal Dentate Granule Cells.

Maintaining low [Cl - ] in is important for inhibitory function, however, hyperactivity, such as that seen in epilepsy, may lead to elevated [Cl - ] in. Pilocarpine induces hyperactivity in dentate granule cells (DGCs) in hippocampal organotypic slice cultures. Multicellular imaging using a chloride sensing dye with a fluorescence lifetime imaging approach revealed that [Cl - ] in is elevated in a subpopulation of DGCs. Gaussian mixture model analysis is a powerful tool for studying the emergence of cellular heterogeneity in a pathological condition.

Effect of gamma and neutron irradiations on the physical, magnetic and electrical properties of Ni–Cu–Cd nano-ferrites

The physical, magnetic and electrical properties variations for the sol-gel auto combustion synthesized Ni0.3Cu0.2Cd0.5Fe2O4 by gamma (γ) and neutron irradiations dose applications are studied in this research. The irradiation have been done through 2.0 × 1011 and 1.9 × 1012 cm−2s−1 per min fast neutron flux and γ rays from the research reactor of TRIGA MARK-II and 64 KCi cylindrical 60Co source respectively within room temperature. The rate of 1 Mrad and 3 Mrad dose is 1.067 Mrad/h. XRD results show greater intensities for the irradiation doses. Due to the redistribution of ions, changes in the lattice constant have been found by the irradiation through the results of XRD and Rietveld Refinement process. The saturated magnetization obtained from the VSM is found to decrease first by the irradiation and then increase drastically. This analysis is performed by the popular pulse field technique of hysteresis loop for nano ferrites and further analyzed by LAS. The frequency dependent characteristics such as dielectric constant, electric modulus, impedance analysis and ac conductivity are inspected for all samples with both types of irradiation process. The electrical modulus Cole-Cole plots insure the dominant property as electric stiffness for investigated ferrties. Extreme decrease has been found in the dielectric natures which also show good agreement in the higher ac conductivity nature at the higher frequencies. Electrical parametric dependent overlapping two semicircles which are not complete have been found in the plots of Cole-Cole for impedance data. The energy of activation for the process of diffusion decreases by the irradiation.

Revealing the Chemical and Structural Complexity of Electrochemical Ion Exchange in Layered Oxide Materials.

Soft chemistry techniques, such as ion exchange, hold great potential for the development of battery electrode materials that cannot be stabilized via conventional equilibrium synthesis methods. Nevertheless, the intricate mechanisms governing ion exchange remain elusive. Herein, we investigate the evolution of the long-range and local structure, as well as the ion (de)intercalation mechanism during electrochemical Li-to-Na ion exchange initiated from an O3-type lithium-layered oxide cathode. The in situ-formed mixed-cation electrolyte leads to competitive intercalation of Li and Na ions. While Li ion intercalation predominates at the beginning of initial discharge, Na ion cointercalation into a different layer results in ion redistribution and phase separation, with the emergence of a P3-Na phase alongside an O3-Li phase. Further, this study spatially resolves the heterogeneous nature of electrochemical ion exchange reactions within individual particles and provides insights into the correlations between local Ni redox processes and phase separation. Overall, electrochemical ion exchange leads to a mixed-phase cathode and alters its reaction kinetics. Those findings have important implications for the development of new metastable materials for renewable energy devices and ion separation applications.

A perturbative multi-mode model with finite parallel electric field for fast-ion-driven Alfvén eigenmodes

Abstract Alfvén eigenmodes are of great interest in any fusion device as they can be excited by fast ions in the plasma. If the modes grow to large amplitudes, they can cause transport and redistribution of the fast ions, thus limiting fusion performance. To save computational resources, the resonant kinetic interaction between the fast-particle species and the modes is often modelled by MHD-kinetic hybrid codes. Here, we present such a hybrid model which is applicable to three-dimensional magnetic fields, accounts for a finite parallel electric field and multiple MHD modes present at the same time. The model extends the one previously implemented in the CKA-EUTERPE code allowing for a better estimate of the damping due to the parallel electric field and nonlinear mode-mode interaction. The capabilities of our model are illustrated by applying the code to model nonlinear frequency chirping and fast-ion profile flattening.

Solution-Processed Polymer Memcapacitors with Stimulus-Controlled and Evolvable Synaptic Functionalities: From Short-Term Plasticity to Long-Term Plasticity to Metaplasticity.

In the vanguard of neuromorphic engineering, we develop a paradigm of biocompatible polymer memcapacitors using a seamless solution process, unleashing comprehensive synaptic capabilities depending on both the stimulation form and history. Like the human brain to learn and adapt, the memcapacitors exhibit analogue-type and evolvable capacitance shifts that mirror the complex flexibility of synaptic strengthening and weakening. With increasing frequency and intensity of the stimulation, the memcapacitors demonstrate an evolution from short-term plasticity (STP) to long-term plasticity (LTP), and even to metaplasticity (MP) at a higher level. A physical picture, featuring the stimulus-controlled spatiotemporal ion redistribution in the polymer, elaborates the origin of the memcapacitive prowess and resultant versatile synaptic plasticity. The distinctive MP behavior endows the memcapacitors with a dynamic learning rate (LR), which is utilized in an artificial neural network. The superiority of implementing a dynamic LR compared with conventional practices of using constant LR shines light on the potential of the memcapacitors to exploit organic neuromorphic computing hardware.

Nonlinear simulations of GAEs in NSTX-U

A set of nonlinear simulations has been performed in order to study the nonlinear evolution of unstable global Alfvén eigenmodes in the National Spherical Torus Experiment-Upgrade (NSTX-U). Results of the single toroidal mode number, n, simulations are compared with a full nonlinear simulation (all toroidal harmonics included). In single-n simulations, the conservation of two integrals of motion of a particle in a cyclotron resonance with a monochromatic wave is demonstrated, resulting in a one-dimensional evolution of the particle distribution in (E,μ,pϕ) phase-space. Nonlinear simulations (both single-n and full nonlinear) show a significant redistribution of the resonant fast ions, especially in the pitch parameter. Thus, the changes in the resonant particle's parallel and perpendicular energies can be several times larger than the total particle energy change, with only a small fraction transferring into the excitation of the mode itself. This implies that even a relatively small amplitude mode can significantly modify the beam distribution in the resonant region. For the NSTX-U case considered, the single-n simulation results are close to full nonlinear simulation only for the most unstable mode, in which case the saturation amplitudes and changes in the fast ion distribution are comparable. In contrast, peak amplitudes of subdominant modes in all-n simulations are smaller by a factor of 3–10 compared to single-n runs due to the flattening of the beam ion distribution by the fastest growing mode.

Emerging role of MXene in energy storage as electrolyte, binder, separator, and current collector: A review

Numerous energy storage parts can benefit from valuable and unique properties of MXenes. MXenes serve a variety of purposes in batteries and supercapacitors, including substrates for electrodeposition, steric hindrance, ion redistribution, bilayer and oxidation/reduction ion storage, ion transfer regulation, and more. They have been used to improve the performance and stability of separators, electrolytes and electrodes. Here, we discuss about various MXene preparation methods, its numerous physicochemical properties, and then present some recent studies in which MXene-based materials have been used as electrolytes, separators, current collectors, and binders in energy storage devices. Finally, we provide an outlook on the prospects and challenges associated with energy storage device components based on MXene and probable direction for future applications.

Applied Electric Field Effects on Diffusivity and Electrical Double-Layer Thickness.

This study utilizes molecular dynamics (MD) simulations and continuum frameworks to explore electroosmotic flow (EOF) in nanoconfined aqueous electrolytes, offering a promising alternative to conventional micro-/nanofluidic systems. Although osmotic behavior in these environments is deeply linked to local fluid properties and interfacial dynamics between the fluid and electrolyte solutions, achieving a complete molecular-level understanding has remained challenging. The findings establish a linear relationship between electric field strength and fluid velocity, uncovering two distinct transport regimes separated by a critical threshold, with a markedly intensified flow in the second regime. It is demonstrated that rising electric field strengths significantly enhance water diffusion coefficients, supported by a detailed analysis of fluid hydration structures, the potential of mean force (PMF), and local stress tensors. Due to the applied electric field strength, the motion of ions and water accelerates, leading to the redistribution of ions and intensification of electrostatic forces. This expands the thickness of the electric double layer (EDL) and amplifies fluid diffusivity, thereby enhancing nanoscale fluid activity. These insights enhance the molecular-level understanding of EOF and define the stability of flow regimes, providing valuable guidelines for advancing nanofluidic technologies, such as drug delivery systems and lab-on-a-chip devices.

Efficient mitigation of lithium dendrite by two-dimensional A-type molecular sieve membrane for lithium metal battery

Uneven lithium deposition poses a primary challenge for lithium-ion batteries, as it often triggers the growth of lithium dendrites, thereby significantly compromising battery performance and potentially giving rise to safety concerns. Therefore, the high level of safety must be guaranteed to achieve the large-scale application of battery energy storage systems. Here, we present a novel separator design achieved by incorporating a two-dimensional A-type molecular sieve coating onto the polypropylene separator surface, which functions as an effective lithium ion redistribution layer. The results demonstrated that even after undergoing 1000 cycles, the cell equipped with a two-dimensional A-type molecular sieve-Polypropylene (2D-A-PP) separator still maintains an impressive capacity retention rate of 70 %. In contrast, cells equipped with Polypropylene (PP) separators exhibit capacity retention rates below 50 % after only 500 cycles. Additionally, the incorporation of a two-dimensional molecular sieve enhances the mechanical properties of the PP separator, thereby bolstering battery safety. This study proposes a novel concept for the design of lithium-ion battery separator materials, offering a fresh perspective on the development of separators with exceptional thermal stability, enhanced porosity, superior electrolyte affinity, and effective inhibition of lithium dendrite formation.

Self‐Selective Crossbar Synapse Array with n‐ZnO/p‐NiOx/n‐ZnO Structure for Neuromorphic Computing

AbstractArtificial synapse devices are essential elements for highly energy‐efficient neuromorphic computing. They are implemented as crossbar array architecture, where highly selective synaptic weight updates for training and sneak leakage‐free inference operations are required. In this study, self‐selective bipolar artificial synapse device is proposed with n‐ZnO/p‐NiOx/n‐ZnO heterojunction, and its analog synapse operation with high selectivity is demonstrated in 32 × 32 crossbar array architecture without the aid of selector devices. The built‐in potential barrier at p‐NiOx/n‐ZnO junction and the Zener tunneling effect provided nonlinear current–voltage characteristics at both voltage polarities for self‐selecting function for synaptic potentiation and depression operations. Voltage‐driven redistribution of oxygen ions inside n–p–n oxide structure, evidenced by x‐ray photoelectron spectroscopy, modulated the distribution of oxygen vacancies in the layers and consequent conductance in an analog manner for the synaptic weight update operation. It demonstrates that the proposed n–p–n oxide device is a promising artificial synapse device implementing self‐selectivity and analog synaptic weight update in a crossbar array architecture for neuromorphic computing.

Fabrication of Isotope-Enriched Nanostructures Using Ultrafast Laser Pulses under Ambient Conditions for Biomolecular Sensing.

Recent advances in the use of stable isotopes necessitate novel synthesis techniques for isotope separation and enrichment that are scalable and offer high throughput. Stable-isotope-enriched nanostructures can offer unique advantages as nanomedicines, safe tracers, and labels and are critical for applications in various industrial processes, metabolic research, and medicine. So far, there exists no method to synthesize miniature isotope-enriched materials at the nanoscale. In this study, an ultrafast Laser-induced isotope enrichment at nanoscale (LIIEN) is put forward to synthesize isotope-enriched nanostructures, eliminating the need for large equipment and expenses, thereby demonstrating a lab-scale isotope enrichment process. A significant isotope enrichment for Carbon nanostructures is observed. The isotope enrichment can be attributed to the redistribution of isotope ions in the plasma plume explained by the plasma centrifuge model. The LIIEN synthesized structures exhibit excellent Surface-Enhanced Raman Scattering (SERS)signal enhancement and reproducibility, making them potential candidates for SERS-based biomolecule sensing. This technique is an efficient method to fabricate nanosized isotope-enriched structures of characteristic properties by carefully tuning laser parameters at ambient conditions.

Memristive Characteristics in an Asymmetrically Charged Nanochannel.

The emergent nanofluidic memristor provides a promising way of emulating neuromorphic functions in the brain. The conical-shaped nanopore showed promising features for a nanofluidic memristor, inspiring us to investigate the memory effects in asymmetrically charged nanochannels due to their high current rectification, which may result in good memory effects. Here, the memory effects of an asymmetrically charged nanofluidic channel were numerically simulated by Poisson-Nernst-Planck equations. Our results showed that the I-V curves represented a diode in low scanning frequency and then became a memristor and finally a resistor as frequency increased. We successfully replicated the learning behavior in our system with history-dependent ion redistribution in the nanochannel. Some critical factors were quantitatively analyzed for the memory effects including voltage amplitude, optimal frequency, and Dukhin number. Experimental characterizations were also carried out. Our findings are useful for the design of nanofluidic memristors by the principle of enrichment and depletion as well as the determination of the best memory settings.

Revealing the characteristics of oxygen evolution reaction performance of NiZn ferrites

Magnetic field-assisted method has been proved as an effective method to improve oxygen evolution reaction performance (OER) of water splitting, however, the essential reason for the improvement of OER performance still remains unclear. Herein, Ni1-xZnxFe2O4 ferrites were prepared by the combination of hydrothermal and calcination method, the magnetic properties, oxygen evolution reaction performance and the effect of applied magnetic field on OER performance were studied and discussed according to the magnetic properties and ion site situation. The magnetic field effect depended on the applied magnetic field strength and the magnetic magnetization density of catalysts, it was attributed to changes of electron state and redistribution of ions in the spinel structure. The overpotential decreased by approximately 50 mV and its double layer capacitance increased about 60 % at 125 mT applied magnetic field. The results provided a newness research view for the domain of electrochemistry.

A universal pre-charging method for enhancing transient speed in Organic Electrochemical Transistors

Organic electrochemical transistors (OECT) have shown great potential in diverse applications; however, in many OECTs, their slow transient response has thus far limited their practical use. One reason for the slow response is the complex interplay between lateral and vertical ion transport that has so far been poorly understood. In this work, we study the impact of lateral ion transport on OECT transient response, introduce a robust pre-charging method to manipulate the slow lateral ion transport. This approach leads to quicker ion redistribution and improved switching speeds. We show the general utility of pre-charging method in enhancing the switching speeds across various material systems, characterized by both low and high ion mobilities, and across different device architectures, achieving nearly symmetric speeds for both on-switching and off-switching. Moreover, we showcase the efficacy of the pre-charging method in enabling slow OECTs to capture rapid signals in real-world applications. Our findings present a groundbreaking strategy for enhancing the response times of OECT devices and deepening our understanding of the transient mechanisms in OECT device.

Effect of rare earth (Ho and Er) co-substitution on the magnetic and dielectric properties of nanocrystalline cobalt ferrites

Nanocrystalline cobalt ferrites co-substituted with rare earth Ho and Er (CoFe2-2xHoxErxO4, 0 ≤x≤0.10) have been synthesized via the sol-gel method. X-ray Diffraction (XRD) confirmed the single-phase spinel structure with reduced crystallite sizes (65 nm–12 nm), micro-strain (ε) and increased lattice constant (a) with Ho–Er co-substitution. Rietveld refinement and theoretical computation revealed Ho and Er occupancy at octahedral sites and Fe and Co ions redistribution between the tetrahedral and octahedral sites. Infrared spectroscopy, Field Emission Scanning Electron Microscopy (FESEM), Energy Dispersive X-ray spectroscopy (EDX) and X-ray Photoelectron Spectroscopy (XPS) supported the formation of the desired spinel structure, aggregated spherical morphology, chemical stoichiometry and elemental states. Magnetic measurements showed a systematic decrease in saturation magnetization (Ms), magnetocrystalline anisotropy (K1), coercivity (Hc) and Curie temperature (Tc) with Ho–Er co-substitution. Electron Spin Resonance (ESR) exhibited asymmetric resonance peaks, reduced resonance field (Hr), linewidth (ΔHpp) and deviation in Lande g values. Impedance spectroscopy revealed two conduction mechanisms (holes and electrons) with distinct activation energies (EaI and EaII). Modulus spectrum analysis confirmed the thermally activated sample-electrode effects and the Nyquist plots indicated the dominant contribution of the grain boundary resistance to the conduction process. A notable enhancement in the dielectric constant (ε′) was observed with Ho–Er co-substitution. The ac conductivity (σac) followed the Jonscher Power Law (JPL). The temperature-dependent frequency exponent s(T), suggests the existence of two conduction mechanisms: non-overlapping small polaron tunneling (NSPT) and correlated barrier hopping (CBH).

Bilayer piezoionic sensors for enhanced detection of dynamic, static, and directional forces with self-healing capabilities

Electronic skin (e-skin) aims to replicate the tactile feedback mechanism of natural skin, offering great potential across robotics, healthcare monitoring, and human-machine interfaces. Traditional e-skin systems utilize electron-based sensing through capacitance and piezoresistivity for static forces, and piezoelectricity and triboelectricity for dynamic forces. However, the former group struggles with dynamic stimuli and external power dependencies, while the latter excels in self-powering but fails in static detection. Addressing these gaps, iontronics emerges as a versatile solution, providing innovative avenues for energy harvesting, sensing, and actuation through ion redistribution in response to varied stimuli, but shows limitations in output signals and response times. We report herein the development of bilayerstructured piezoionic materials with significantly enhanced output signal and response time. The piezoionic bilayer structure not only harnesses an ion accumulation interface, leading to amplified output signals and fast response times, but also exhibits an ion-dipole interactive self-healing property. Our sensor generates a signal output of 95 mV and features a quick response time of 30 ms, with an impressive self-healing capability of ∼100%. It demonstrates the ability to accurately detect both static and dynamic forces, including specific movements like bending and vibrations, maintaining its robustness through 8000 cycles of repetitive deformation. Its utility is further proven in a practical setting with a braille reader device, highlighting its potential for incorporation into a wide array of soft, autonomous iontronic systems that require enhanced sensitivity, rapid detection capabilities, and self-sustainability.

Study of the cationic substitution effect on the magnetic properties of the ferrite MnxZn1-xFe2O4 nanoparticles prepared by TREG-mediated solvothermal route

MnxZn1-xFe2O4 (x = 0–1) solid solution was prepared using the TREG-mediated solvothermal method. 10–12 nm spherical superparamagnetic particles (except for ZnFe2O4) were obtained. At room temperature, the ferrites have lower magnetic saturation (Ms) than magnetite. However, at 10 K, it is precisely the opposite. DRX and EXAFS showed that incorporating Zn2+ ions in tetrahedral A-sites provokes a redistribution of Mn and Fe ions in octahedral B-sites of the mixed spinel structure. For Zn concentrations from x = 0.5 and below, the Mn and Fe ions are almost equally distributed between A and B-sites. Therefore, at low Zn concentrations, the small migration of Fe and Mn ions to B-sites increases the magnetic moment of B sub-lattices and, consequently, the total magnetic saturation. In addition, Mn2+ oxidized to Mn3+ and, simultaneously, Fe3+ reduced to Fe2+, affecting the magnetic properties. The increment of Zn concentration severely reduces the magnetization.

Influence of sawtooth oscillations on fast ions in a stellarator

Sawtooth oscillations in tokamaks frequently lead to the redistribution of energetic ions, mainly on passing orbits, causing their expulsion from the core. This paper discusses the first measurements of the interaction of fast ions and sawteeth in the Large Helical Device. The crashes were caused by the plasma current induced by Electron Cyclotron Current Drive and Neutral Beam Current Drive. Despite these crashes, there was no detectable redistribution effect on fast ions in either the core or at the edge of the plasma.

Spatiotemporal dynamic temperature variation dominated by ion behaviors during groundwater remediation using direct current

Direct current (DC) electric field has shown promising performance in contaminated site remediation, in which the Joule heating effect plays an important role but has been previously underappreciated. This study focuses on the spatiotemporal characteristics and mechanism of temperature change in heterogeneous porous media with applied DC. The heating process can be divided into four phases: preferential heating of the low permeability zone (LPZ), rapid heating in the middle region, temperature drop and hot zone shift, and reheating. The dynamic ion behaviors with complex interplays among reactions, electrokinetic-driven migration, and mixed convection induced an uneven redistribution of ions and dominated the heating rate and temperature distribution. The concentration of major ions near the pH jump decreased to 1% of the initial value, even though ions were continuously pumped into the heating zone. This ion depletion caused a drop in current, heating rate, and temperature. Here ions cannot be delivered rapidly into the ion-depleted zone by electromigration due to the potential flattening in the surrounding region. The presence of LPZ intensified the nonuniformity of ion redistribution, where a regional focusing of water-soluble ions was observed, and weakened the temperature rebound compared with that using homogeneous sand. These results provide a new perspective on the regulation of DC heating in site remediation.