Local Electric Field Research Articles

Turbulence Embedded Into the Ionosphere by Electromagnetic Waves

AbstractWhen charged particles are accelerated from Earth's magnetosphere and precipitate into the atmosphere, their impact with neutral gas creates the aurora. Structured electric fields drive the acceleration processes but they are also passed down to the ionosphere, meaning that turbulence can in part be embedded into the ionosphere rather than emerge through instability processes locally. Applying a point‐cloud analysis technique adapted from observational cosmology, we show how observed turbulence in the ionosphere matches electrical current signatures in the pulsating aurora in a series of conjunctions between space‐ and ground‐based instruments. We propose that the temporal spectrum of pulsations in the pulsating aurora is the driver of a clearly observed energy injection into the ionosphere's unstable bottomside. Precipitating electrons produce electric fields through charge deposition, and we observe wave characteristics that are present in this pattern. Next, the relative electron‐ion drifts excite the Farley‐Buneman instability, the distribution of whose waves are organized according to the local electric field. It is the temporal characteristics of chorus wave interactions in the magnetosphere that is imparted, via precipitating electrons, to the pulsating aurora, and so we propose that chorus wave interactions are capable of embedding turbulent structure into the ionosphere. This structure (now pressure gradients) dissipate energy in the E‐region through turbulent processes, observed by the icebear coherent scatter radar.

An Infrared Nanospectroscopy Technique for the Study of Electric-Field-Induced Molecular Dynamics.

Static electric fields play a considerable role in a variety of molecular nanosystems as diverse as single-molecule junctions, molecules supporting electrostatic catalysis, and biological cell membranes incorporating proteins. External electric fields can be applied to nanoscale samples with a conductive atomic force microscopy (AFM) probe in contact mode, but typically, no structural information is retrieved. Here we combine photothermal expansion infrared (IR) nanospectroscopy with electrostatic AFM probes to measure nanometric volumes where the IR field enhancement and the static electric field overlap spatially. We leverage the vibrational Stark effect in the polymer poly(methyl methacrylate) for calibrating the local electric field strength. In the relevant case of membrane protein bacteriorhodopsin, we observe electric-field-induced changes of the protein backbone conformation and residue protonation state. The proposed technique also has the potential to measure DC currents and IR spectra simultaneously, insofar enabling the monitoring of the possible interplay between charge transport and other effects.

Diffusosphere engineering in BNT-based multilayer heterogeneous film capacitors for high performance

Combining layers with high breakdown resistance and high polarization is a promising approach for designing dielectric capacitors with high energy density and efficiency. However, such combinations often accompany strong interfacial polarization, magnification of local electric fields, leading to premature breakdown. This work addresses this issue via controlled formation of diffusospheres. We constructed multilayer heterogeneous films using two Bi0.5Na0.5TiO3 (BNT)-based substances with high breakdown resistance and high polarization properties. Experimental results and finite element simulations demonstrate that the energy storage capacity of these films effectively harnesses the advantages of both phases. Notably, the interface polarization is minimal. Instead, a solid solution-like diffusosphere, formed by the mutual diffusion of ions between the two phases, plays a crucial role. The diffusosphere acts as a transition zone, mitigating charge aggregation at the interfaces and optimizing the relaxor and breakdown characteristics of the capacitor. With six diffusospheres, the multilayer heterogeneous capacitor achieves a recoverable energy storage density of 94 J/cm3, a significant advancement in BNT-based energy storage films. This work proposes and validates the concept of diffusospheres and their role in reducing interfacial polarization in multilayer heterogeneous films, enhancing the understanding of heterogeneous composite structures and advancing the field of dielectric energy storage.

Local Electric Field Accelerates Zn2+ Diffusion Kinetics for Zn‐V Battery

AbstractVanadium‐based aqueous zinc‐ion batteries (AZIBs) exhibit significant potential for large‐scale energy storage applications, attributed to their inherent safety characteristics. Addressing the slow transport kinetics of divalent Zn2+ within the cathode lattice, thereby enhancing the rate capability and stability, is essential for the Zn‐V battery system. In this study, a local electric field (LEF) strategy is introduced to accelerate the Zn2+ diffusion by creating abundant oxygen vacancies (Ov) in V2O5. Comprehensive characterization and density functional theory (DFT) calculations reveal the formation of the Ov induced atomic‐level donor‐acceptor couple configuration, verify and visualize the LEF. The fabricated LEF‐enhanced vanadium oxide (LEF‐VO) exhibits exceptional rate capability, achieving 338.3 mA h g−1 at a current density of 10 A g−1, and maintaining 66.4% of its capacity over a range from 0.2 to 20 A g−1. Furthermore, the influence of the LEF on expediting Zn2+ diffusion kinetics is elucidated, correlating to the electrical force. This novel LEF approach offers valuable insights for advancing high‐rate cathode materials.

Application of Gap Mode Ultrasensitive P-GERTs in SERS-Based Rapid Detection

In surface-enhanced Raman scattering (SERS) detection research, the shape, structure, surface modification, and material selection of nanoparticles can significantly impact the SERS intensity. Petal-like gap-enhanced Raman tags (P-GERTs) possess numerous sharp tips and edges, which generate localized electric field enhancements, further amplifying the electric field enhancement effect on neighboring molecules and enhancing the SERS signal. Additionally, the surface of P-GERTs can be modified with functional molecules, enabling their application in the detection of disease biomarkers. Using COVID-19 as an example, the performance of P-GERTs in disease biomarker detection was validated, demonstrating that the signal intensity of this probe can reach 55 times that of regular gold nanoparticles and 36.7 times that of smooth shell gap-enhanced Raman tags (S-GERTs). Furthermore, in combination with magnetically retrievable magnetic bead substrates, the N-protein antigen was specifically detected in a one-step process. N-protein was detected within 15 min using a portable Raman spectrometer. The limit of detection (LOD) for the standard sample was 4.28 pg/mL, and the LOD for the actual throat swab sample system was 25.4 pg/mL. This workflow can be extended to the detection of other biomarkers, making it widely applicable.

Highly sensitive near-field leakage-enhanced optical fiber SPR sensor based on gold nanoarrays modulation

A novel near-field leakage-enhanced optical fiber surface plasmon resonance (NLF-SPR) sensor based on the synergistic sensitization of cuboid gold nanoarrays and WSe2 film is proposed for the first time to our knowledge. The sensor is composed of a side-polished multimode fiber, a continuous gold film, a continuous tungsten selenide (WSe2) film, and well-arranged cuboid gold nanoarrays. The sensor leverages the high carrier mobility characteristic of the WSe2 film, the near-field leakage enhancement arising from the nanoarrays structure, and the localized electric field enhancement property introduced by nanotips to enhance the refractive index sensitivity. In order to optimize the spectral characteristic, the modulation of electric field distribution and spectral characteristic by the structural parameters of gold nanoarrays is investigated through three-dimensional (3D) finite element simulation. Results show that in the refractive index range of 1.3332–1.3432 refractive index unit (RIU), the average sensitivity of the NLF-SPR sensor can reach up to 10108 nm/RIU, and the highest sensitivity can reach up to 14692.46 nm/RIU. The average sensitivity and the highest sensitivity are 1.87 times and 2.56 times higher, respectively, than those of the side-polished fiber SPR sensor with a monolayer gold film. Furthermore, the experimental results demonstrate that the near-field leakage enhancement introduced by gold nanoarrays improves the performance of the fiber SPR sensor, resulting in a 49.3 % increment in sensitivity. The experimental results are in agreement with the trend of the simulation results. Even better performance improvements have been achieved compared to existing methods and a more flexible approach to performance tuning is provided. With the maturity and development of various nanoarray processing techniques such as focused ion beam, electron beam lithography, and nanoimprint lithography, the proposed NLF-SPR sensor has the potential to be fabricated on a large scale and is expected to be widely employed in biomedical, clinical applications, and other fields.

Local Excitation of Kagome Spin Ice Magnetism Seen by Scanning Tunneling Microscopy.

The kagome spin ice can host frustrated magnetic excitations by flipping its local spin. Under an inelastic tunneling condition, the tip in a scanning tunneling microscope can flip the local spin, and we apply this technique to kagome metal HoAgGe with a long-range ordered spin ice ground state. Away from defects, we discover a pair of pronounced dips in the local tunneling spectrum at symmetrical bias voltages with negative intensity values, serving as a striking inelastic tunneling signal. This signal disappears above the spin ice formation temperature and has a dependence on the magnetic fields, demonstrating its intimate relation with the spin ice magnetism. We provide a two-level spin-flip model to explain the tunneling dips considering the spin ice magnetism under spin-orbit coupling. Our results uncover a local emergent excitation of spin ice magnetism in a kagome metal, suggesting that local electrical field induced spin flip climbs over a barrier caused by spin-orbital locking.

Piezoelectric Analgesia Blocks Cancer-Induced Bone Pain.

The manipulation of cell surface receptors' activity will open a new frontier for drug development and disease treatment. However, limited by the desensitization of drugs, effective physical intervention strategy remains challenging. Here, the controllable internalization of transient receptor potential vanilloid 1 (TRPV1) on neural cells by local piezoelectric field is reported. Single-cell-level local electric field is construct by synthesizing piezoelectric BiOIO3 nanosheets (BIONSs). Upon a mild ultrasound of 0.08Wcm-2, an electric field of 15.29µV is generated on the surface of BIONSs, further inducing TRPV1 internalization in 5min. The as-downregulated TRPV1 expression results in the reduction of Ca2+ signal in a spinal neuron and the inhibition of the activity of wide range dynamic neurons, therefore effectively preventing the transmission of cancer-induced bone pain (CIBP). This strategy not only charts a new course for CIBP alleviation, but also introduces a promising nanotechnology for regulating cell surface receptors, showing significant potential in neuropathological and receptor-related diseases.

Spatially engineered local electric field for enhanced water electrolysis

Alkaline water electrolysis (AWE) stands as a well-established and promising route for sustainable hydrogen production. However, traditional AWE cells suffer from low performance and bulky size. Here, we introduce the integrated design, a streamlined architecture that maximizes space utilization and enhances inter-component contact. This geometric innovation requires only minor modifications in the manufacturing process to effectively double the gas production capacity without increasing the volume of the device across a wide voltage range. Utilizing Ni foam electrodes, the device achieves a 205 mA cm−3 output at 2.0 V. Through visual inspections and simulations, we compared the new and traditional designs, attributing performance improvements to optimized local electric fields. These findings not only demonstrate the feasibility of spatial engineering, but also illuminate a promising path to advance alkaline water electrolyzer technology.

Topologically-protected optical bistability based on two-dimensional photonic crystal L6 nanocavity dimer array

We numerically investigate the optical bistability from a two-dimensional photonic crystal L6 nanocavity dimer array structure configured under the Su-Schrieffer-Heeger model. The localized electric field in the topological edge state is highly enhanced, which gives rise to strong nonlinear phenomena such as optical bistability. In comparison, a topologically trivial nanocavity is also designed and its field strength distribution and optical bistable response are also simulated. In order to test the robustness, three types of defects and interferences are introduced in both the topologically non-trivial and trivial cavities. Benefiting from the topological feature, the proposed topological cavity exhibits superior optical bistable performance with low threshold power and high switching contrast compared to that in the trivial cavity. Our work suggests what we believe to be a novel avenue toward the insertion of optical bistable devices with high robustness into future photonic integrated circuits and photonic neural networks.

Employing lattice compression spin polarization electric field for boosting degradation of mixed antibiotics in wastewater

Localized polarization electric field is a key factor affecting photocatalytic activity. In this study, the localized polarization electric field of lattice strain was introduced into the electronic structure of Bi2WO6 by using the high and low valence state doping method. The impurity energy level induced by lattice strain further affects the gap energy level. As an intermediate state for electron transfer, the gap level further promotes the dynamics of photo generated charges, reducing the band gap by 0.4 eV and improving the photoelectric performance by 60 %. Various tests and theoretical calculations have confirmed that the internal electric field of local polarization significantly improves the generation and transfer rate of photo-generated charges, thereby boosting catalytic activity. The removal ratios of ciprofloxacin (CIP) and tetracycline (TC) in the mixed wastewater reach 91.5 % and 97.1 % in 90 min, respectively. Cyclic tests have shown that the electronic structure control exhibits excellent stability with removal ratios of CIP and TC of 83.9 % and 85.7 %, respectively. Finally, the 8C of CIP and the 11C and 19O of TC are most susceptible to the attack of free radicals generated by lattice compression spin polarization electric fields based on the theoretical calculations of the Fukui function and the analysis of intermediates. This work provides new insights into the design of catalysts for efficient photo generated charge dynamics with lattice strain.

Near-infrared detection based on the excitation of hot electrons in Au/Si microcone array

Although the photoresponse cut-off wavelength of Si is about 1100 nm due to the Si bandgap energy, the internal photoemission effect (IPE) of the Au/Si junction in Schottky detector can extend the absorption wavelength, which makes it a promising candidate for the Si-based infrared detector. However, due to low light absorption, low photon–electron interaction, and poor electron injection efficiency, the near-infrared light detection efficiency of the Schottky detector is still insufficient. The synergistic effect of Si nano/microstructures with a strong light trapping effect and nanoscale Au films with surface plasmon enhanced absorption may provide an effective solution for improving the detection efficiency. In this paper, a large-area periodic Si microcone array covered by an Au film has successfully been fabricated by one-time dry etching based on the mature polystyrene microspheres lithography technique and vacuum thermal deposition, and its properties for hot electron-based near infrared photodetection are investigated. Optical measurements show that the 20 nm-thick Au covered Si microcone array exhibits a low reflectance and a strong absorption (about 85%) in wide wavelength range (900–2500 nm), and the detection responsivity can reach a value as high as 17.1 and 7.0 mA W−1 at 1200 and 1310 nm under the front illumination, and 35.9 mA W−1 at 1310 nm under the back illumination respectively. Three-dimensional finite difference time domain (3D-FDTD) simulation results show that the enhanced local electric field in the Au layer distributes near the air/Au interface under the front illumination and close to the Au/Si interface under the back illumination. The back illumination favors the injection of photo-generated hot electrons in Au layer into Si, which can explain the higher responsivity under the back illumination. Our research is expected to promote the practical application of Schottky photodetectors to Si-compatible near infrared photodetectors.

Quantifying Induced Dipole Effects in Small Molecule Permeation in a Model Phospholipid Bilayer.

The cell membrane functions as a semipermeable barrier that governs the transport of materials into and out of cells. The bilayer features a distinct dielectric gradient due to the amphiphilic nature of its lipid components. This gradient influences various aspects of small molecule permeation and the folding and functioning of membrane proteins. Here, we employ polarizable molecular dynamics simulations to elucidate the impact of the electronic environment on the permeation process. We simulated eight distinct amino-acid side chain analogs within a 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine bilayer using the Drude polarizable force field (FF). Our approach includes both unbiased and umbrella sampling simulations. By using a polarizable FF, we sought to investigate explicit dipole responses in relation to local electric fields along the membrane normal. We evaluate molecular dipole moments, which exhibit variation based on their localization within the membrane, and compare the outcomes with analogous simulations using the nonpolarizable CHARMM36 FF. This comparative analysis aims to discern characteristic differences in the free energy surfaces of permeation for the various amino-acid analogs. Our results provide the first systematic quantification of the impact of employing an explicitly polarizable FF in this context compared to the fixed-charge convention inherent to nonpolarizable FFs, which may not fully capture the influence of the membrane dielectric gradient.

Hierarchical Modeling of the Local Reaction Environment in Electrocatalysis.

ConspectusElectrocatalytic reactions, such as oxygen reduction/evolution reactions and CO2 reduction reaction that are pivotal for the energy transition, are multistep processes that occur in a nanoscale electric double layer (EDL) at a solid-liquid interface. Conventional analyses based on the Sabatier principle, using binding energies or effective electronic structure properties such as the d-band center as descriptors, are able to grasp overall trends in catalytic activity in specific groups of catalysts. However, thermodynamic approaches often fail to account for electrolyte effects that arise in the EDL, including pH, cation, and anion effects. These effects exert strong impacts on electrocatalytic reactions. There is growing consensus that the local reaction environment (LRE) prevailing in the EDL is the key to deciphering these complex and hitherto perplexing electrolyte effects. Increasing attention is thus paid to designing electrolyte properties, positioning the LRE at center stage. To this end, unraveling the LRE is becoming essential for designing electrocatalysts with specifically tailored properties, which could enable much needed breakthroughs in electrochemical energy science.Theory and modeling are getting more and more important and powerful in addressing this multifaceted problem that involves physical phenomena at different scales and interacting in a multidimensional parametric space. Theoretical models developed for this purpose should treat intrinsic multistep kinetics of electrocatalytic reactions, EDL effects from subnm scale to the scale of 10 nm, and mass transport phenomena bridging scales from <0.1 to 100 μm. Given the diverse physical phenomena and scales involved, it is evident that the challenge at hand surpasses the capabilities of any single theoretical or computational approach.In this Account, we present a hierarchical theoretical framework to address the above challenge. It seamlessly integrates several modules: (i) microkinetic modeling that accounts for various reaction pathways; (ii) an LRE model that describes the interfacial region extending from the nanometric EDL continuously to the solution bulk; (iii) first-principles calculations that provide parameters, e.g., adsorption energies, activation barriers and EDL parameters. The microkinetic model considers all elementary steps without designating an a priori rate-determining step. The kinetics of these elementary steps are expressed in terms of local concentrations, potential and electric field that are codetermined by EDL charging and mass transport in the LRE model. Vital insights on electrode kinetic phenomena, i.e., potential-dependent Tafel slopes, cation effects, and pH effects, obtained from this hierarchical framework are then reviewed. Finally, an outlook on further improvement of the model framework is presented, in view of recent developments in first-principles based simulation of electrocatalysis, observations of dynamic reconstruction of catalysts, and machine-learning assisted computational simulations.

Pilot Study on the Production of Negative Oxygen Ions Based on Lower Voltage Ionization Method and Application in Air Purification

In the current highly industrialized living environment, air quality has become an increasing public health concern. Natural environments like forests have excellent air quality due to high concentrations of negative oxygen ions originating from low-voltage ionization, without harmful ozone. Traditional negative oxygen ion generators require high voltage for corona discharge to produce ions. However, high voltage can increase electron collisions and excitations, leading to more dissociation and recombination of oxygen molecules and consequently higher ozone production. To address the challenge of generating negative oxygen ions without accompanying ozone production, this study designed and constructed a low-voltage negative oxygen ion generator based on nanometer-tip carbon fiber electrodes. The advantage of this device lies in the high curvature radius of carbon fibers, which provides high local electric field strength. This allows for efficient production of negative oxygen ions at low operating voltages without generating ozone. Experiments demonstrated that the device can efficiently generate negative oxygen ions at a working voltage as low as 2.16 kV, 28% lower than the lowest voltage reported in similar studies. The purification device manufactured in this study had a total decay constant for PM2.5 purification of 0.8967 min−1 within five minutes, compared to a natural decay constant of only 0.0438 min−1, resulting in a calculated Clean Air Delivery Rate (CADR) of 0.1535 m3/min. Within half an hour, concentrations of PM2.5, PM1, PM10, formaldehyde, and TVOC were reduced by 99.09%, 99.40%, 99.37%, 94.39%, and 99.35%, respectively, demonstrating good decay constants and CADR. These findings confirm its effectiveness in improving indoor air quality, highlighting its significant application value in air purification.

Boosting visible-light-driven photocatalytic H2 production by optimizing surface hydrogen desorption of NiS/CdS–P photocatalyst

Metal chalcogenides are regarded as favorable H2-evolution cocatalysts; however, they often exhibit unfavorable H desorption characteristics due to the strong affinity of nascent H and highly electronegative S sites, which significantly inhibit H2 generation. To address this issue, a general approach to electron-enriched control of sulfur-active sites is developed for weakening the strong interaction of S–H bonds. This is achieved through the formation of a nanostructured model composed of NiS/CdS–P, in which the surface phosphorus (P) atoms are incorporated in CdS NRs to create an imbalanced charge distribution and a localized built-in electric field in the crystal structure of CdS. In this situation, the built-in electric field not only separates the photogenerated electron hole pairs, but it also accelerates the photogenerated electrons from the CdS–P conduction band to the NiS surface for rapid hydrogen reduction rather than hydrogen adsorption. Photocatalytic tests show that the resultant NiS/CdS–P photocatalyst displays a significant H2-generation rate of 44.39 mmol g−1 h−1 and an apparent quantum efficiency of 41% at 420 nm. Valance band XPS analysis shows that CdS–P has a higher electron density than CdS, leading to the production of electron-rich Sδ− active centers. This better photocatalytic hydrogen generation might be due to the synergistic impact of tailoring the intrinsic built-in electric field for the acceleration of photogenerated charges by P-doping and the fabrication of a NiS cocatalyst for hydrogen reduction rather than hydrogen adsorption. The concept of optimizing the electron densities of active sites by morphology tailoring, with an extra built-in electric field, gives a method for rationally constructing artificial photocatalysts for solar power conversion.

Individual Addressing and State Readout of Trapped Ions Utilizing Radio-Frequency Micromotion.

Excess "micromotion" of trapped ions due to the residual radio-frequency (rf) trapping field at their location is often undesirable and is usually carefully minimized. Here, we induce precise amounts of excess micromotion on individual ions by adjusting the local static electric field they experience. Micromotion modulates the coupling of an ion to laser fields, ideally tuning it from its maximum value to zero as the ion is moved away from the trap's rf null. We use tunable micromotion to vary the Rabi frequency of stimulated Raman transitions over two orders of magnitude, and to individually control the rates of resonant fluorescence from three ions under global laser illumination without any changes to the driving light fields. The technique is amenable to situations where addressing individual ions with focused laser beams is challenging, such as tightly packed linear ion strings or two-dimensional ion arrays illuminated from the side.

Ultralow electric-field poling of LiNbO3 single-crystal devices

The LiNbO3 (LNO) single crystal receives wide applications in nonvolatile memories, surface acoustic wave devices, and electro-optic modulators. However, engineering of antiparallel domain patterns within micrometer-sized devices generally requires a poling voltage more than a few thousands of volts. The high poling voltage could invoke dielectric breakdown. Here, we found an effective method to increase the local electric field significantly for domain nucleation at the interfaces of an etched LNO mesa in contact to two concave side electrodes, while the electric field across the protruding intra-electrode area can be lower by 10 times after the metal diffusion at the surface. Subsequent piezoresponse force microscopy mapping shows the nucleating domains to grow up through the entire intra-electrode area. This method is universal and analogous to other ferroelectric devices for the realization of low-voltage operations.

An Anti-Scaling Strategy for Electrochemical Wastewater Treatment: Leveraging Tip-Enhanced Electric Fields.

Electrode scaling poses a critical barrier to the adoption of electrochemical processes in wastewater treatment, primarily due to electrode inactivation and increased internal reactor resistance. We introduce an antiscaling strategy using tip-enhanced electric fields to redirect scale-forming compounds (e.g., Mg(OH)2 and CaCO3) from the electrode-electrolyte interface to the bulk solution. Our study utilized Cu nanowires (Cu NW) with high-curvature nanostructures as the cathode, in contrast to Cu nanoparticles (Cu NP), Cu foil (CF), and Cu mesh (CM), to evaluate the electrochemical nitrate reduction reaction (NO3RR) performance in hard water conditions. The Cu NW/CF cathode demonstrated superior NO3RR efficiency, with an apparent rate constant (Kapp) of 1.04 h-1, significantly outperforming control electrodes under identical conditions (Kapp < 0.051 h-1). Through experimental and theoretical analysis, including COMSOL simulations, we show that the high-curvature design of Cu NW induced localized electric field enhancements, propelling OH- ions away from the electrode surface into the bulk solution, thus mitigating scale formation on the cathode. Testing with real nitrate-contaminated wastewater confirms that the Cu NW/CF cathode maintained excellent denitrification efficiency over a 60-day period. This study offers a promising perspective on preventing electrode scaling in electrochemical wastewater treatment, paving the way for more efficient and sustainable practices.

Local Electric Field Driving Selective Formation of High-Valent Co(IV)═O Species by Regulating Coordination Microenvironment of Co Single Atom

Local Electric Field Driving Selective Formation of High-Valent Co(IV)═O Species by Regulating Coordination Microenvironment of Co Single Atom