Strong Electric Field Research Articles

Electrocatalytic reduction of nitrate by Cu valence-regulated heterojunction electrode: A key role of Cu(I/II) composites and high nitrate reduction efficiency

Cu – based composite electrode has aroused great concern among NO3− reduction. There are few reports on the synergistic effect of different Cu valence states. It is not clear how to regulate the valence ratio of copper by or controlling the dosage of reducing agent in the synthesis process. Herein, a Cu(I) and Cu(II) heterogeneous electrode with different Cu valences was prepared to build a Cu(I/II)@NF-UX composite electrode on nickel foam. Urea was used as a gentle reductant to construct the heterogeneous structure of Cu(I) and Cu(II) during a one-step hydrothermal process for in – situ growth of Cu(I/II)@NF-UX, and the ratio between Cu(I) and Cu(II) and the microstructure were adjusted by changing the amount of urea added during the preparation process. The strong NO3− adsorption effect of traditional Cu – based electrode is still maintained in the Cu(I/II)@NF composite. The strong interfacial electric field constructed in the Cu(I/II) heterostructure efficiently promoted the electron transfer, and the electrons subsequently reduced the NO3− directly or helped form the atomic H* for NO3− indirect reduction. More importantly, there is almost no accumulation of NO2− and NH4+, efficient and stable nitrate reduction (93.2%) was achieved and 96.2% N2 selectivity was achieved with the help of electric chlorination. It is worth noting that the high pH adaptability, low energy consumption, good stability, and low Cu/Ni leaching would make the Cu(I/II)@NF composite electrode have an excellent application prospect for NO3− removal engineering.

Interfacial [S─Cu─C] Bonds Induced π-d Electron Coupling Toward Modulating Charge Transfer for Efficient Solar Water Oxidation.

Regulating the interfacial electric field to achieve rapid charge transfer is crucial for superior photoelectrochemical water splitting. Herein, the ultra-thin hydrogen-substituted graphdiyne (HsGDY) is precisely assembled on the surface of CdS nanorod array (Cu-CdS-HsGDY) by an in situ polymerization strategy. The strong π-d electron coupling is aroused by the delocalized π electrons of HsGDY and the delocalized d electrons of CdS through the interfacial [S─Cu─C] bonds. The strong interfacial electric field can effectively promote the charge localization distribution and reduce the charge transfer resistance. The optimized Cu-CdS-HsGDY photoanode obtain a photocurrent density as high as 4.83 mA cm-2 at 1.23 V versus reversible hydrogen electrode in neutral electrolyte solution under AM 1.5G illumination, which is 6.8 times that of the pristine CdS. Moreover, the photoanode maintains an initial photocurrent density of 84% within 4 h without any assistance of sacrificial agents, which is a rather competitive performance of similar sulfide photoanodes. The mechanism of strong π-d electron coupling on interfacial charge transfer and surface reaction kinetics is investigated by transient spectroscopy measurements, density functional theory calculation, and finite element simulation analysis. This work provides new insights into designing a reasonable interface structure to regulate charge transfer for achieve efficient PEC water splitting.

Unveiling Frequency-Dependent Electromechanical Dynamics in Ferroelectric BaTiO3 Nanofilm with a Core-Shell Structure

Diverse domain patterns significantly influence the nonlinear electromechanical behaviors of ferroelectric nanomaterials, with polarization switching under strong electric fields being inherently a frequency-dependent phenomenon. Nevertheless, research in this area remains limited. In this study, we present a phase-field investigation of frequency-dependent electromechanical dynamics of a polycrystalline BaTiO3 nanofilm with a core-shell structure, subjected to applied frequencies ranging from 1 to 80 kHz. Our findings elucidate the microstructural mechanisms underlying the electromechanical behaviors observed in these materials. The effect of the grain size and the strains effect are also taken into account. Hysteresis and butterfly loops exhibit a marked change in shape as the frequency changes. We discuss the underlying domain-switching dynamics as a basis for evaluating such frequency-dependent properties. In addition, we examine the scaling behaviors of the dynamic hysteresis and the influence of grain boundaries on the domain structure. We can also observe from hysteresis loops that the remnant polarization and coercive field significantly diminish when grain sizes decrease from 60 to 5 nm. A smaller grain size of the nanofilm yields a larger percentage of the dielectric grain boundary, which “dilutes” the overall ferroelectricity of the film. A vortex domain structure is more likely to form at low frequency and a small grain size.

Interface-Engineered CuxO@Bi2MoO6 Heterojunctions to Inhibit Piezoelectric Screening Effect and Promote Double-Nanozyme Catalysis for Antibacterial Treatment.

Sonodynamic therapy is confronted with the low acoustic efficiency of sonosensitizers, and nanozymes are accompanied by intrinsic low catalytic activity. Herein, to increase the piezopotential of N-type piezoelectric semiconductors, the P-N heterojunction is designed to inhibit the piezoelectric screening effect (PSE) and increase electron utilization efficiency to enhance nanozyme activity. P-type CuxO nanoparticles are in situ grown on N-type piezoelectric Bi2MoO6 (BMO) nanoflakes (NFs) to construct heterostructured CuxO@BMO by interface engineering. CuxO deposition leads to lattice distortion of BMO NFs to improve piezoelectric response, and the strong interface electric field (IEF) suppresses PSE and increases piezopotential. The nonlocal piezopotential, local IEF, and glutathione (GSH) inoculation enhances electron-hole separation and increases peroxidase (POD)-like activity of BMO and GSH oxidase (GSHOx)-like activity of CuxO with high selectivity. The heterojunction formation causes the transfer and rearrangement of interface electrons, and the increased piezopotential accelerates electron transfer at interfaces with bacteria, thus increasing the production of reactive oxidative species and interfering with adenosine triphosphate synthesis. The heterostructured nanozymes produce abundant intracellular ·OH and achieve 4log magnitude reductions in viable bacteria and effective biofilm dispersion. This study elucidates integral mechanisms of nanozyme and acoustic catalysis and opens up a new way to synergize high piezopotential and nanozyme-catalyzed therapy.

Construction of a MoOx/MoS2 Heterojunction via the Surface Sulfurization of the Oxide and Its Photocurrent-Switching Characteristics in the Range of the Broadband Light Spectrum

In order to utilize the longer wavelength light, the surface sulfurization of MoO3 was carried out. The photocurrent responses to typical 650, 808, 980, and 1064 nm light sources with Au gap electrodes were investigated. The results showed that the surface S–O exchange of MoO3 improved the interfacial charge transfer in the range of the broadband light spectrum. The S and O can be exchanged on the surface of MoO3 nanosheets under the hydrothermal condition, leading to the formation of a surface MoOx/MoS2 heterojunction. The interfacial interaction between the MoO3 nanosheets and MoS2 easily generated free electrons and holes, and it effectively avoided the recombination of photogenerated carriers. Meanwhile, the surface S-doping of MoO3 also resulted in the generation of an oxygen vacancy and sulfur vacancy on MoO3−xS2−y. The plasmonic characteristics of MoO3−x contributed to the enhancement of the interfacial charge transfer by photoexcitation. Otherwise, even with zero bias applied, a good photoelectric signal was still obtained with polyimide film substrates and carbon electrodes. This indicates that the formation of the heterojunction generates a strong built-in electric field that drives the photogenerated carrier transport, which can be self-powered. This study provides a simple and low-cost method for the surface functionalization of some metal oxides with a wide bandgap.

Impact of electron velocity modulation on microwave power performance for AlGaN/GaN HFETs

In this study, we demonstrate the effects of electron velocity modulation (Δve/ΔVgs) on the microwave power performance for AlGaN/GaN HFETs. In order to conduct the experiments, AlGaN/GaN HFETs with gate lengths ranging from 500 to 80 nm were fabricated. Electron transport was investigated by coupling a drift-diffusion solver with the Monte Carlo method. As gate lengths (Lg) varied from 500 to 200 nm, the increased polarization Coulomb field scattering led to an increase in Δve/ΔVgs and the stronger electric field (E) increased ve and enhanced the transconductance (gm), which in turn led to a greater power gain (Gp) in the HFETs. The higher power output (Pout) was also due to the increased ve that boosted the saturated output current (Ids,sat). The unique phenomenon that occurs from electron velocity modulation of AlGaN/GaN HFETs at electron densities (ns) < 3.42 × 1012cm−2 can be used as an effective mechanism to enhance the power gain of AlGaN/GaN HFETs.

Effects of Ion Valence States and Radii on the Performance of Solid-State PEDOT:PSS Electrochromic Devices.

Ion transport is a critical factor influencing the performance of electrochromic devices (ECDs). In this work, the effects of the valence state and ionic radius of six cations, Li+, Na+, K+, Mg2+, Zn2+, and Al3+, on the performance of poly(3,4-ethylenedioxythiophene)-polystyrene sulfonic acid (PEDOT:PSS)-based ECDs are investigated. Both ion migration and diffusion are discussed as processes that were analyzed, with results indicating that the primary contributor to the response of ECDs is ion migration. The response time decreases with increasing ionic valence and ionic radius, with the valence state having the predominant effect on response speed. Multivalent ions, due to strong electric field forces, migrate more rapidly and intercalate fewer ions at equivalent reaction charges, thereby facilitating a faster response. ECDs with larger-radius ions, which exhibit slower diffusion rates, also achieve faster response speeds. Among the tested ECDs with various electrolytes, the Al3+-based ECD demonstrates the fastest colored/bleached response time of 0.36/0.4 s. In addition, ions with larger radii introduce greater steric hindrance and structural damage during insertion and extraction, leading to ion retention issues and reduced cycling stability. After 500 cycles (2025 s) under a square wave voltage of ±1.5 V, the peak current of ECDs with Li+ (0.60 Å) electrolyte decreased by only 5.07/5.66%, whereas for K+ (1.33 Å) electrolyte, the decrease was 11.55/12.37%. ECDs utilizing small-radius, higher-valence ions, such as Al3+, achieved both fast response and high cycling stability, with peak current reductions of only 6.98/5.01%. Additionally, the charge storage dynamics were examined by analyzing the contributions from surface-controlled and diffusion-controlled charges, further confirming that ion migration dominates in ECDs. The high contribution of surface-controlled charges (80%) supports the fast response of ECDs and contributes to the high coloration efficiency (592.6 cm2/C for Al3+-based devices).

Microscale Templating of Functional Particles Using Self-Limiting Electrospray Deposition.

Electrospray deposition (ESD) uses strong electric fields applied to solutions and dispersions exiting a capillary to produce charged monodisperse droplets driven toward grounded targets. Self-limiting electrospray deposition (SLED) is a phenomenon in which highly directed, uniform, and even 3D coatings can be achieved by trapping charge in the deposited film, redirecting the field lines to uncoated regions of the target. However, when inorganic particles are added to SLED sprays, the buildup of charge required to repel incoming material is disrupted as particle loading increases. Due to its fibril gelling behavior, methylcellulose (MC) SLED can form nanowire morphologies. These wires, when used as a binder, can separate particles and prevent percolation. In this work, a variety of conductive and insulating particles are explored using patterned and un-patterned substrates. This exploration allows us to maximally load particles for high-concentration and highly controlled self-limiting functional sprays. This is demonstrated using Ti3C2Tx MXene to functionalize an interdigitated electrode for use as a supercapacitor.

Fabrication and Mechanism Insight of Multidimensional Coupled Metal-Free van der Waals Heterostructures for Enhanced Photocatalytic Hydrogen Evolution.

It is an arduous issue to significantly improve the charge separation efficiency of polymer photocatalysts due to their inherently high exciton binding energy. Herein, based on an interfacial coupling and atom diffusion strategy, a metal-free 3D/2D van der Waals (VdW) heterojunction is fabricated through the modification of rich-vacancy wrinkle-like S8 (Vs-S8) microspheres on the surface of S-doped polymeric carbon nitride (S-PCN) nanosheets. The insight into the mechanism reveals that the interfacial coupling effect induces a strong built-in electric field from S-PCN to Vs-S8, and the carrier transfer behavior abides by the type-II charge transfer pathway, thereby dramatically improving the separation efficiency and transport kinetics of photogenerated carriers. As a result, the as-prepared metal-free 3D/2D Vs-S8/S-PCN VdW heterojunction is endowed with more superior photocatalytic hydrogen evolution (PHE) performance than PCN. The highest average PHE rate is about 11.3 times higher than that of PCN, and the apparent quantum efficiency reaches 30.1% at 400 nm on the optimal 3%-Vs-S8/S-PCN sample. This work contributes a new design strategy for a metal-free VdW heterojunction and provides a feasible avenue for improving the carrier separation efficiency of polymer photocatalysts.

Construction of 2D/2D Pd Metallene/COFs System with Strong Internal Electric Field for Outstanding Solar Energy Photocatalysis.

Due to the severe recombination of charge carriers, the photocatalytic activity of covalent organic frameworks (COFs) materials is limited. Herein, through simple ultrasound and stirring processes, the Pd metallene (Pde) is successfully combined with 2D COFs to form Pde/TpPa-1-COF (Pde/TPC) composites. Obviously, a strong internal electric field (IEF) is successfully formed in Pde/TPC hybrid materials, which significantly boosts the separation of photogenerated charges. In addition, the matched 2D structure of the two materials can also lead to electronic coupling effects, plentiful active sites, and shortened carrier migration paths. Thus, the Pde/TPC hybrid materials own extraordinary carrier separation ability with a longer carriers lifetime (3.3 ns for Pde/TPC and 2.7 ns for TPC), which can be proved series of photoelectrochemical and spectroscopic tests. Benefiting from the formation of IEF and the matched 2D structure, the 8% Pde/TPC demonstrates the highest photocatalytic H2 evolution efficiency, with H2 production rate reaching up to 5.85 mmolg-1h-1, which is over 25 times greater than that of pristine COFs, also exceeding that of many reported COFs-based photocatalysts. This research provides new perspectives and innovative approaches to further research on enhancing the internal electric field of COFs to promote their photocatalytic performance.

DBD plasma induced SMOSI and encapsulation for regulation of Brønsted-Lewis acid sites of Cr-MOFs@ZrO2

Dielectric barrier discharge (DBD) plasma for the synthesis of Zr-MOFs followed by the calcination and combination with Cr-MOFs was presented to prepare a Brønsted-Lewis bifunctional catalyst for the conversion of glucose to 5-hydroxymethylfurfural (HMF). The strong electric field on the catalyst surface formed by DBD plasma induced the enhancement of strong metal oxide support interaction (SMOSI), which could be indicated by XPS. SMOSI could change the embedding degree of metal micro-particles. SMOSI accompanied with the encapsulation of Zr metal nanoparticles could regulate the acid sites of the catalysts. Lewis acid played an important role in the isomerization of glucose to fructose, while Brønsted acid played a key role in the further conversion of glucose. The strong Brønsted acid sites determined the conversion of glucose to HMF. Cr-MOFs@ZrO2-D with the DBD plasma method afforded a higher Brønsted to Lewis acid ratio, compared with Cr-MOFs@ZrO2-S with the hydrothermal method. Glucose conversion of 97.9 % and HMF yield of 38 % were obtained with DMF solvent system and Cr-MOFs@ZrO2-D at 150 °C for 2h. This research provided a new method for preparing Zr-MOFs by DBD plasma and a new idea to comprehensively understand the role of Brønsted and Lewis acid sites in glucose conversion.

Ionospheric Disturbances Observed Over the Peruvian Sector During the Mother's Day Storm (G5‐Level) on 10–12 May 2024

AbstractThis article presents the recent extreme and rare G5‐level geomagnetic storm (Mother's Day Storm) effects on the equatorial and low‐latitude ionosphere observed at the Peruvian sector by the Jicamarca (11.9°S, 76.8°W, magnetic dip 1°N) incoherent scatter radar and associated instruments. This storm was produced by multiple Earth‐directed coronal mass ejections, which generated significant modifications in the Earth's magnetic field, leading to the Sym‐H of ∼−518 nT. On the dayside, due to the strong eastward penetration electric field, vertical plasma drift and equatorial electrojet (EEJ) enhanced for 2–3 hr and remained consistent at values of ∼95 m/s and 260 nT between 1700 and 1900 UT (1200 and 1400 LT). At the same time, vertical E B plasma drift uplifted the equatorial ionosphere, producing the dusk‐side super plasma fountain and transferring electron density to higher latitudes. A huge increase (∼1,325%) in electron density (from 11 to 142 TECu) is observed at low and mid‐latitudes from ∼20°S to 50°S between 2000 and 0400 UT (1500–2300 LT). The strong westward penetration electric field suppressed pre‐reversal enhancement, leading to downward plasma drift (∼−96 m/s) at around 2400 UT (1900 LT). Overnight, vertical plasma drift fluctuated between ±90 m/s, and the combined effect of penetration and disturbance dynamo electric fields caused a significant increase (∼530 km) in ionospheric virtual height. In the main and early recovery phase, consistent short‐ and long‐duration electric field disturbances persisted for approximately 30 hr, with periods of ∼48 and 90 min.

Rational design of ZnO/SrTiO3 S-scheme heterojunction for photo-enhanced piezocatalytic hydrogen production

Photopiezocatalysis have been frequently investigated for hydrogen evolution reactions in recent years. Herein, ZnO, SrTiO3 and ZnO/SrTiO3 S-scheme heterojunction were investigated for photo/piezocatalytic hydrogen production. Piezocatalytic hydrogen production under ultrasonic vibration by using ZnO, SrTiO3 and ZnO/SrTiO3 was obtained as 270 µmol g-1h−1, 200 µmol g-1h−1 and 1265 µmol g-1h−1, respectively. In addition, ZnO/SrTiO3 S-scheme heterojunction showed 2200 µmol g-1h−1 photopiezocatalytic hydrogen production under simultaneous exposure to white LED light and ultrasonic sound. ZnO/SrTiO3 heterojunction displayed significantly higher hydrogen production rate due to the decreased charge recombination, increased charge transfer with strong piezoelectric polarization and internal electrical field. The piezoelectric effect of ZnO/SrTiO3 heterojunction is also confirmed by piezoresponse force microscope technique with butterfly and phase hysteresis loops. Also, piezoelectric coefficient of ZnO/SrTiO3 found about 2-folds higher than those of their pristine forms. Electron transfer and reaction mechanism of ZnO/SrTiO3 and activity differences are confirmed by advanced optical and electrochemical techniques such as diffuse reflectance spectroscopy, electronic impedance spectroscopy, Mott-Schottky calculation and chronoamperometry. The whole electrochemical measurements have been performed with or without mechanical stress and light irradiation, which signify their band bending properties, electron transfer mechanism and catalytic activities.

Magnetic field and photon co-enhanced S-scheme MXene/In2S3/CoFe2O4 heterojunction for high-performance lithium-oxygen batteries

Under the spotlight for their potential to reduce over-potential, photo-assisted Li–O2 batteries still face a key challenge: the rapid recombination of photo-generated electron-hole pairs, which limits their efficiency. In this study, we address this limitation by designing a Li–O2 battery that integrates both photo and magnetic field assistance, using an S-scheme MXene/In2S3/CoFe2O4 heterojunction photocathode. This unique combination enhances visible light absorption and generates a strong built-in electric field, facilitating effective charge separation and boosting photocatalytic activity. During discharge, photo-generated electrons participate in the oxygen reduction reaction, while photo-induced holes contribute to the decomposition of discharge products during charging. Furthermore, the introduction of a magnetic field, confirmed through vibrating sample magnetometer, Mössbauer spectroscopy, X-ray absorption near edge structure, and cyclic voltammetry analyses, enhances electron-hole separation via Lorentz forces and spin–orbit coupling, accelerating the formation and decomposition of Li2O2. With this synergistic approach, the battery achieves a high specific capacity of 26500 mAh g−1, ultra-low oxygen reduction/evolution reaction over-potentials of 0.08 V/0.17 V, and a long cycle life of 2000 cycles with energy efficiency of 98.11 %. This work demonstrates the promising potential of combining photo and magnetic field effects to improve the electrochemical performance of Li–O2 batteries, opening new avenues for high-performance energy storage systems.

Overestimation of Astrophysical Gamma-Ray Energies during Thunderstorms: Synergy of Galactic and Atmospheric Accelerators

Particle accelerators abound in space plasmas, saturating the cosmos with fully stripped nuclei and gamma rays, with energies surpassing the capabilities of human-made accelerators by orders of magnitude. Upon reaching Earth’s atmosphere, these particles trigger extensive air showers (EASs), generating millions of secondary cosmic rays of lower energies. Free electrons from EASs developing in the atmosphere are seeds for atmospheric electron accelerators. Strong atmospheric electric fields (AEFs) evolving during thunderstorms act as accelerators, amplifying the intensity of electrons many times, significantly enlarging the EAS size (number of electrons). Thus, the energy of the primary cosmic ray recovered by EAS size can be significantly overestimated. Recently discovered by high-altitude EAS arrays, PeVatron candidates (ultra–high-energy (UHE) astrophysical gamma-ray sources) must be carefully examined according to the atmospheric conditions during EAS detection. Large High Altitude Air Shower Observatory and High-Altitude Water Cherenkov Observatory arrays are located in regions of frequent thunderstorms, and an AEF’s strength can reach and surpass the critical strength to start relativistic runaway electron avalanches. A few registered UHE gamma rays from stellar sources can be registered at just this time when the AEF highly enhances the EAS size. Thunderstorm ground enhancements are copiously registered at mountain peaks of Eastern Europe, Germany, and Armenia, with energies well above the threshold energy of EAS array scintillators. Thus, the overestimation of the energy of primary particles is not an exotic process but a consequence of already well-established physical phenomena. Consequently, a report on each registered UHE gamma ray should include the recorded time and corresponding weather conditions.

Kinetics of optical phonons and DP depolarization of spins in drift transport: Hot carrier spin effect in semiconductors

<p>Spin-<strong>c</strong>onserving transport of carriers is an essential requirement for the practical semiconductor-based spintronic devices. Kinetics of optical phonons and Dyakonov-Perel (DP) depolarization of spins in drift transport in semiconductor gallium arsenide (GaAs) is theoretically investigated<strong>. </strong>We consider electrons in <em>n</em>-type bulk GaAs subjected to a strong electric field, where the electron distribution is assumed to be drifted Maxwellian. The momentum drift of this distribution results in the enhanced drift velocity, and electrons with the corresponding energy emit optical hot phonons in the drifting process. The hot phonons are incorporated via the longitudinal polar optical phonon (POP) mechanism in the momentum relaxation. It is found that a finite phonon lifetime can reduce the momentum relaxation rate, which results in a delay in the runaway to higher fields, where the effect increases with the electron density. The electron spin is found to relax with the DP relaxation frequencies, and the DP spin lifetimes are found to decrease with increasing the drift field. However, a high field completely depolarizes the electron spin due to an increase of the DP spin precession frequency of the hot electrons in the POP scattering process. It is also found that the DP spin precession frequency decreases with decreasing electron temperature or increasing electron density in the moderate range. However, the findings resulting from this investigation demonstrate the hot carrier effect in the spin transport in semiconductors. The results are discussed in comparison with those obtained in earlier experimental and theoretical studies with different approaches.</p>

Wafer-Scale Semitransparent MoS2/WS2 Heterojunction Catalyst on a Silicon Photocathode for Efficient Hydrogen Evolution.

The development of catalysts that are optically transparent, electrically charge-transferable, and capable of protecting underlying photoactive semiconductors is crucial for efficient photoelectrochemical (PEC) hydrogen production. However, meeting all these requirements simultaneously poses significant challenges. In this study, the fabrication of a wafer-scale transparent bilayer MoS2/WS2 catalyst is presented with a staggered heterojunction, optimized for photon absorption, extraction of photogenerated charge carriers, and surface passivation of p-Si photocathode. The MoS2 and WS2 monolayers are grown via metal-organic chemical vapor deposition, followed by sequential transfer and stacking onto the p-Si photocathode. The resulting type-II heterojunction film establishes a strong built-in electric field for rapid charge carrier transport and effectively protects the Si surface from oxidation and corrosion. The fabricated MoS2/WS2/p-Si photocathode demonstrates outstanding PEC performance, achieving a high photocurrent density of -25mAcm-2 at 0V versus reversible hydrogen electrode, along with enhanced stability compared to monolayer MoS2/p-Si. This work provides promising strategies for developing optically transparent, electrically active, and protective catalysts for practical PEC energy conversion systems.

Photoexcitation‐Enhanced High‐Ionic Conductivity in Polymer Electrolytes for Flexible, All‐Solid‐State Lithium‐Metal Batteries Operating at Room Temperature

Designing solid polymer electrolytes (SPEs) with high ionic conductivity for room‐temperature operation is essential for advancing flexible all‐solid‐state energy storage devices. Innovative strategies are urgently required to develop SPEs that are safe, stable, and high‐performing. In this work, we introduce photoexcitation‐modulated heterojunctions as catalytically active fillers within SPEs, guided by photocatalytic design principles, and employ natural bacterial cellulose to enhance the mechanical properties of the inorganic‐filled SPEs. In‐situ photothermal experiments and theoretical calculations reveal that the strong photogenerated electric field produced by trace heterojunctions within poly(ethylene oxide) electrolytes under photoexcitation significantly enhances lithium salt dissociation, increasing the concentration of mobile Li+. This results in a substantial increase in ionic conductivity, reaching 0.135 mS cm−1 at 25 °C, with a Li+ transference number as high as 0.46. The flexible all‐solid‐state lithium‐metal pouch cells exhibit an impressive discharge capacity of 178.8 mAh g−1 even after repeated bending and folding, and demonstrate exceptional long‐term cycling stability, retaining 86.7% of their initial capacity after 250 cycles at 1 C (25 °C). This research offers a novel approach to developing high‐performance flexible lithium‐metal batteries.

Multi-scale and time-resolved structure analysis of relaxor ferroelectric crystals under an electric field

Lead-based relaxor ferroelectrics exhibit giant piezoelectric properties owing to their heterogeneous structures. The average and local structures measured by single-crystal X-ray diffraction under DC and AC electric fields are reviewed in this article. The position-dependent local lattice strain and the distribution of polar nanodomains and nanoregions show strong electric field dependence, which contributes to the giant piezoelectric properties.

Deriving the Ionospheric Electric Field From the Bulk Motion of Radar Aurora in the E‐Region

AbstractIn the auroral E‐region strong electric fields can create an environment characterized by fast plasma drifts. These fields lead to strong Hall currents which trigger small‐scale plasma instabilities that evolve into turbulence. Radio waves transmitted by radars are scattered off of this turbulence, giving rise to the ‘radar aurora’. However, the Doppler shift from the scattered signal does not describe the F‐region plasma flow, the drift imposed by the magnetosphere. Instead, the radar aurora Doppler shift is typically limited by nonlinear processes to not exceed the local ion‐acoustic speed of the E‐region. This being stated, recent advances in radar interferometry enable the tracking of the bulk motion of the radar aurora, which can be quite different and is typically larger than the motion inferred from the Doppler shift retrieved from turbulence scatter. We argue that the bulk motion inferred from the radar aurora tracks the motion of turbulent source regions (provided by auroras). This allows us to retrieve the electric field responsible for the motion of field tubes involved in auroral particle precipitation, since the precipitating electrons must drift. Through a number of case studies, as well as a statistical analysis, we demonstrate that, as a result, the radar aurora bulk motion is closely associated with the high‐latitude convection electric field. We conclude that, while still in need of further refinement, the method of tracking structures in the radar aurora has the potential to provide reliable estimates of the ionospheric electric field that are consistent with nature.