Charge-discharge Rate Research Articles

Improving the Energy Storage Performance in Bi0.5Na0.5TiO3-Based Ceramics by Combining Relaxor and Antiferroelectric Properties.

Ceramic capacitors have received great attention for use in pulse power systems owing to their ultra-fast charge-discharge rate, good temperature stability, and excellent fatigue resistance. However, the low energy storage density and low breakdown strength (BDS) of ceramic capacitors limit the practical applications of energy storage technologies. In this work, we present a series of relaxor ferroelectric ceramics (1-x) [0.94 Bi0.5Na0.5TiO3 -0.06BaTiO3]- x Sr0.7Bi0.2TiO3 (1-x BNT-BT- x SBT; x = 0, 0.20, 0.225, 0.25, 0.275 and 0.30) with improved energy storage performances by combining relaxor and antiferroelectric properties. XRD, Raman spectra, and SEM characterizations of BNT-BT-SBT ceramics revealed a rhombohedral-tetragonal phase, highly dynamic polar nanoregions, and a reduction in grain size with a homogeneous and dense microstructure, respectively. A high dielectric constant of 1654 at 1 kHz and low remnant polarization of 1.39 µC/cm2 were obtained with the addition of SBT for x = 0.275; these are beneficial for improving energy storage performance. The diffuse phase transition of these ceramics displays relaxor behavior, which is improved with SBT and confirmed by modified the Curie-Weiss law. The combining relaxor and antiferroelectric properties with fine grain size by the incorporation of SBT enables an enhanced maximum polarization of a minimized P-E loop, leading to an improved BDS. As a result, a high recoverable energy density Wrec of 1.02 J/cm3 and a high energy efficiency η of 75.98% at 89 kV/cm were achieved for an optimum composition of 0.725 [0.94BNT-0.06BT]-0.275 SBT. These results demonstrate that BNT-based relaxor ferroelectric ceramics are good candidates for next-generation ceramic capacitors and offer a potential strategy for exploiting novel high-performance ceramic materials.

Unleashed Remarkable Energy Storage Performance in Bi0.5K0.5TiO3-based Relaxor Ferroelectrics by Local Structural Fluctuation.

Dielectric capacitors harvest energy through an electrostaticprocess, which enables an ultrafast charging-discharging rate and ultrahigh power density. However, achieving high energy density (Wrec) and efficiency (η) simultaneously, especially when preserving them across a wide frequency/temperature range or cycling numbers, remains challenging. In this work, by especially introducing NaTaO3 into the representative ferroelectric relaxor of Bi0.5K0.5TiO3-Bi0.5Na0.5TiO3 and leveraging the mismatch between B-site atoms, we proposed a method of enhancing local structural fluctuation to refine the polar configuration and to effectively improve its overall energy-storage performances. As a consequence, the ceramic exhibits an ultrahigh Wrec of 15.0 J/cm3 and high η up to 80%, along with a very wide frequency stability of 10 - 200 Hz and extensive cycling number up to 108. In-depth local structure and chemical environment investigations, consisting of atom-scale electron microscopy, neutron total scattering, and solid-state nuclear magnetic resonance, reveal that the randomly distributed A/B-site atom pairs emerge in the system, leading to the evident local structural fluctuations and concomitant polymorphic polar nanodomains. These key ingredients contribute to the large polarization, minimal hysteresis, and high breakdown strength, thereby promoting energy-storage performances. This work opens a new path for designing high-performance dielectric capacitors via manipulating local structural fluctuations.

High efficiency deep ultraviolet micro-LED and optical fiber coupling for low power charge management applications

During space gravitational wave detection missions, it is necessary to manage the charge accumulated on the surface of the test mass. A common method involves using optical fibers to transmit ultraviolet (UV) light, leveraging the photoelectric effect for charge management. An important issue in this process is achieving efficient coupling between the UV light source and the optical fiber. In this paper, for the first time we proposed to use DUV micro-LEDs as light sources for charge management systems, which will have lower power consumption. We conducted simulations to investigate the effect of the size ratio between deep ultraviolet (DUV) micro-LEDs and optical fibers on the coupling efficiency. We further employed a direct coupling method to conduct coupling experiments of DUV micro-LEDs and optical fibers with varying wavelengths and sizes. The simulation and experiment results both indicate that, under the influence of both size and divergence angle, there exists an optimal DUV micro-LED size responsible for maximum coupling efficiency between DUV micro-LEDs and optical fibers which is 80 μm when the optical fiber size is 1000 μm. Applying the 80 μm DUV micro-LED in charge management experiments demonstrated the feasibility of using DUV micro-LEDs as light sources for low power charge management systems, achieving rapid charge–discharge rates and high photoelectric current at lower driving electrical power.

Theoretical study on arsenene as anode material for magnesium ion battery in rail transit

The development and regulation of high-performance anode materials contribute to the rapid development of ion batteries in rail transit. In this paper, based on the first-principles calculation method of density functional theory, the properties of two-dimensional arsenene materials are regulated by torsional deformation, and the feasibility of torsionally deformed arsenene as an electrode material for magnesium ion batteries is studied. The results show that the arsenene monolayer remains stable after being adsorbed by a single Mg ion. The properties of arsenene are indirect bandgap semiconductors with a band gap of 1.60 eV. In the current research scope, deformation does not change the semiconductor properties of intrinsic arsenene. As the torsion angle increases, the band gap gradually decreases. The Mg-adsorbed arsenene system exhibits quasi-metallic properties with a band gap of 0.07 eV. The torsional deformation transforms the adsorption system into a small band gap semiconductor. The torsion deformation makes the diffusion energy barrier of magnesium ions on the arsenene monolayer only 0.09 eV, which ensures an excellent charge–discharge rate. The research results provide a theoretical basis for the design of magnesium ion batteries in rail transit.

MnO2‐Infused PAN Carbon Nanofibers Synthesized via Electrospinning for Enhanced Supercapacitor Performance

AbstractSupercapacitors (SCs) are crucial for high‐performance energy storage, offering high power density, swift charge–discharge rates, and durability. The enhancement of their performance hinges on the development of advanced electrode materials. This study presents an innovative method involving polyacrylonitrile (PAN) nanofibers adorned with manganese dioxide (MnO₂) nanoparticles (NPs), created through electrospinning and subsequent thermal treatment. This synergy exploits the extensive surface area and electrical conductivity of PAN nanofibers along with the substantial capacitance of MnO₂. The MnO₂‐coated PAN nanofibers reached an impressive specific capacitance of 247 F g−1 at a scan rate of 10 mVs−1, markedly boosting the efficacy of all‐solid‐state asymmetric SCs. The SCs, incorporating a polyvinyl alcohol (PVA)/potassium hydroxide (KOH) gel electrolyte, exhibited an energy density of 8.2 Wh kg−1 at a power density of 700 W kg−1, preserving 80.4% of their original capacitance after 5000 cycles. This research is pioneering in combining MnO₂ with PAN nanofibers, marking a significant leap forward in supercapacitor technology with enhanced energy storage capacity and prolonged stability. These findings underscore the promise of these composite materials in future energy storage solutions.

Production of rGO based hybrid composite buckypaper cathodes by using copper oxide polysulfide adsorbent for Li-S batteries

Lithium-sulfur batteries are particularly noteworthy for applications requiring large capacity and long battery life. Transition metal oxides have emerged as polar host materials for lithium polysulfides to further modulate the bonding energy with polysulfides and increase the coupling density of the electrodes. Polar metal oxides naturally adsorb polysulfides on their hydrophilic surfaces. In this study, the polysulfide adsorbing ability of CuO against the shuttle effect is utilized. For this purpose, copper(II) oxide (CuO) is used as polysulfide adsorbent and CuO - reduced Graphene Oxide / Sulphur (CuO-rGO/S) hybrid composite buckypaper electrodes are produced as cathodes in Li-S batteries without using binders. In this work, optical, morphological and structural analyzes of composite films were carried out by Fourier transformed infrared spectroscopy (FT-IR), Raman spectroscopy, field emission gun scanning electron microscopy (FEG-SEM), energy dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Brunauer-Emmett-Teller (BET) analysis, respectively. After the CR2032 button cell was assembled using the produced cathode materials, cyclic voltammetry (CV), charge-discharge performance tests, rate capability and electrochemical impedance spectroscopy (EIS) analyzes were performed to investigate the Li-S battery capacities. With the CuO-rGO/S hybrid composite cathode containing 2 % CuO, a discharge capacity of 1205 mAh g−1 was obtained in the first cycle. At the end of the 1000 cycles, the discharge capacity of the cathode was achieved as high as 696 mAh g−1. As a result, the battery capacity of rGO/S-based composite electrodes has been improved by taking advantage of CuO added to the cathode structure to adsorb polysulfides.

Advanced MOF/MXene heterostructure with carbon aerogel to boosts the ions movement in asymmetric supercapacitors and hydrogen production

Supercapacitors represent a promising avenue for advanced energy storage solutions. However, achieving devices that simultaneously possess all the ideal properties, such as high capacitance, fast charge-discharge rates, and excellent cyclability, remains a significant challenge. Herein, a facile approach for fabricating carbon aerogel-induced chromium metal-organic framework (CA@MIL-101) integrated with titanium carbide MXene (CA@MIL-101-(Cr)/Ti3C2Tx) nanocomposites was demonstrated via hydrothermal method. The CA@MIL-101-(Cr)/Ti3C2Tx nanocomposites offer numerous divalent ion active sites and significantly improve charge transfer kinetics, attributed to their interconnected porous structure. This novel anode exhibits an outstanding specific capacity of 1632 Cg-1 with a PVDF binder-based electrode and a high rate of performance. Moreover, a full-cell supercapacitor was developed with carbon aerogel as the cathode and CA@MIL-101 (Cr)/Ti3C2Tx as the anode. With its hierarchical pore structure and functional groups, the CA@MIL-101 (Cr)/Ti3C2Tx anode achieves an energy density of 38 Wh-kg−1, a high-power density of 1280 W-kg−1, and robust anti-self-discharge behavior. The CA@MIL-101 (Cr)/Ti3C2Tx//CA supercapattery uses both adsorption/desorption processes and faradaic reactions for charge storage. The synthesized materials also perform exceptionally well electro-catalytically. This research advances high-performance CA@MIL-101 (Cr)/Ti3C2Tx electrodes, enhances understanding of supercapacitor charge storage, and paves the way for next-generation energy storage technologies.

Advanced CeO2 doped with different elements: A new preparation method and multifunctional properties

Energy demands are increasing daily, driven by the growth of developing countries and their populations. Supercapacitors have been employed extensively in the field of energy in recent years due to their high energy density, rapid charge-discharge rates, and long-lasting structures. In this study, the electrochemical properties of CeO2 varying with different types of additives were investigated. Four different compounds were synthesized using Ba, Er, and Tb. Syntheses were carried out with the sol-gel method, and X-ray diffraction and Raman spectra were used in crystal structure analysis. It was determined that the crystal lattice was cubic and it possessed Ce-O vibration bands and oxygen vacancy structures. Morphological features were determined by field-emission scanning electron microscope and Brunauer–Emmett–Teller analysis. Cyclic voltammetry measurements were performed for electrochemical properties. According to all results, the highest capacitance was calculated as 1752 F g−1 for the Ba-Er-doped ternary CeO2 compound.

Study on the influence of high rate charge and discharge on thermal runaway behavior of lithium-ion battery

With the development of the new energy industry, battery life and rapid charge-discharge capacity have attracted much attention. At the same time, the high temperature inside the cell during high-rate charging and discharging may increase the probability of the battery thermal runaway. This paper studied the thermal runaway reaction of Li-ion batteries under different state of charge (SOC) and charge rates using a self-made experimental platform. The experimental phenomena and the changes in the temperature field were recorded. The key parameters, such as trigger temperature (T1, Lithium battery back thermal runaway triggers temperature), maximum temperature (Tmax),voltage, and mass loss (ML) of thermal runaway, were measured. The morphology changes of electrode materials, the battery remains, and the dynamics of thermal runaway reaction after high rate charge and discharge were further analyzed. The results show that for the 4 C-100 % battery, the T1 and Ea are reduced by 22.6 ℃ and 82.2 %, and the Tmax and maximum mass loss rate (MLRmax) are increased by 218.14 ℃ and five times, compared with the 1 C-50 % battery. With the increase of charge-discharge rate, the thermal stability of the battery decreases, and the gravity degree of accident increases.

Hydrothermally synthesized copper telluride nanoparticles: First approach to flexible solid-state symmetric supercapacitor

Supercapacitors, with their high-power density, rapid charge–discharge rates, and long cycle life, have emerged as promising energy storage devices for numerous applications. Among the various materials explored for supercapacitor electrodes, copper-based chalcogenides have gathered significant attention due to their intriguing electrochemical properties and simple synthesis routes. While there have been thorough investigations in other fields, only a limited number of studies have focused on the specific application of copper telluride nanoparticles as supercapacitors. In this study, we present a novel approach utilizing hydrothermally synthesized copper telluride (Cu2-xTe) nanoparticles as binder-free electrodes on flexible stainless steel (SS) substrates. The Cu2-xTe nanoparticles, with their small particle (38 nm) and highly crystalline structure, enhance charge storage and promotes a pseudocapacitive behavior, resulting in a high specific capacitance [381 F/g (163 mF/cm2) at 2 mV/s] in a 2 M KCl electrolyte solution. Moreover, we studied and explained the distinct contributions of surface-controlled and diffusion-limited processes to the overall charge storage capacity of the electrode. Our pioneering effort includes the fabrication and analysis of flexible, symmetric solid-state supercapacitor devices utilizing Cu2-xTe electrodes with PVA-LiClO4 gel electrolyte. These devices demonstrate an energy density of 11 Wh/kg, a power density of 800 W/kg, and an impressive 85 % retention of cyclic stability after 5000 cycles.

Ultra-small one-dimensional rice-like CoMoO4 nanorods as a promising pseudocapacitive electrode for high-performance supercapacitors

The demand for sustainable energy sources increases as society progresses. Supercapacitors possess a long lifespan, have a high power density, are ecologically sound, and have the ability to rapidly charge and discharge. Among the several binary transition metal oxides (BTMOs), metal molybdates (AMoO4) are notable for their significant redox activity, widespread availability, affordability, and small ecological footprint. The exceptional theoretical capacitance of CoMoO4, resulting from the presence of active cobalt ions, distinguishes it from other materials. However, the synthesis of CoMoO4 in nanostructured forms presents a challenge. This study introduces a straightforward one-pot solvothermal technique for producing ultra-small, one-dimensional (1D) rice-like CoMoO4 nanorods. The electrochemical performance of rice-like CoMoO4 nanorods as a supercapacitor electrode material was thoroughly investigated, along with larger CoMoO4 nanorods made using the hydrothermal process for comparison. The structural, morphological, and surface characteristics of the rice-like CoMoO4 nanorods were comprehensively examined. The nanorods, formed like rice grains, exhibited exceptional ability to store electric charge, with an outstanding specific capacitance of 1608.8 F g−1. They demonstrated remarkable cycling stability, retaining 96 % of their capacitance after numerous charge and discharge cycles, indicating their durability and reliability. The nanorods also exhibited a high rate capability of 71 %, which is crucial for applications that demand quick energy delivery. This capability enables the nanorods to maintain considerable capacitance even at higher charge-discharge rates. The results indicate that rice-like CoMoO4 nanorods can be used as a material in supercapacitors.

Effects of liquid-phase carbon combining surfactant coatings on the performance of LiMn0.2Fe0.8PO4 cathode materials

Efforts to reduce the particle size of LiFexMn1-xPO4 materials and apply conductive carbon coatings have yielded substantial benefits in terms of obtaining lithium-ion batteries (LIBs) with enhanced electrochemical performance. However, LiFexMn1-xPO4 materials with small particle sizes and uniform carbon layers cannot be obtained by the conventional high-temperature solid-phase method, which is the most convenient and applicable method for the industrial-scale preparation of the cathode materials used in commercial LIBs. The present work addresses this issue by applying the cationic surfactant cetyltrimethylammonium bromide (CTAB) in conjunction with LiMn0.2Fe0.8PO4 (LMFP) particles, and obtaining a carbon layer by replacing the conventional in-situ solid-phase carbon coating process with a secondary liquid-phase coating process using sucrose as the carbon source. The CTAB surfactant is observed to be uniformly adsorbed on the surface of LMFP particles, and maintains small LMFP particle sizes by operating as a dispersant preventing their agglomeration. Additionally, the carbon network formed by CTAB pyrolysis acts as an intermediate medium ensuring that the conductive carbon layer is uniformly and firmly adhered to the LMFP particle surfaces at a high preparation temperature of 680°C. This composite carbon layer is demonstrated to enhance lithium-ion transport, while concurrently acting as a barrier interfering with manganese diffusion within the electrolyte during charge-discharge cycling. As a result, the optimal LMFP-based cathode material achieves reversible specific capacities of 160 mAh g−1 and 120 mAh g−1 at charge-discharge rates of 0.1 C and 5 C, respectively, and the capacity retention is 88 % after 500 cycles at 1 C. Hence, the results verify that the proposed surfactant-mediated liquid-phase carbon coating process is an effective method for enhancing the overall electrochemical performance of LMFP-based cathode materials.

Nickel sulfide nanoparticles decorated on carbon spheres derived from Verbena officinalis for high-performance asymmetric all-solid-state flexible supercapacitors

The crafting and development of electrode materials possessing extensive energy storage capacities, alongside their adherence to environmental and economic principles, along with their outstanding capacitive behaviors, stand as pivotal elements in propelling the technological progress of supercapacitors. In this study, we utilized discarded Verbena officinalis (VOCs) as a carbon substrate and successfully synthesized porous hollow carbon spheres through an in-situ hydrothermal method, subsequently depositing NiS nanoparticles to form a shell-like structured material. The optimized VOCs/NiS-3 composite material exhibited an exceptional specific capacitance of 202.8 mAh g−1 at a current density of 1.0 A g−1; it maintained 71 % of its capacitance even at a high current density of 10 A g−1 (144.2 mAh g−1). After enduring 10,000 charge-discharge iterations, the preservation of charge storage capacity was 81.7 %, highlighting the material's outstanding performance in terms of rapid charge-discharge rates and enduring stability. Furthermore, within a PVA/KOH gel electrolyte, we fabricated an asymmetric all-solid-state supercapacitor device that delivered an energy density of 32.58 Wh k g−1 at a power density of 800 W k g−1. The device sustained a capacitance loss rate of 9.9 % and a coulombic efficiency of 96.8 % after 5000 cycles. Even after 3000 repeated bending at 120°, the capacitance retention reached 88.3 %, indicating the device's exceptional specific capacitance, flexibility and longevity. This research offers a renewable and waste-resource recycling design strategy for synthesizing outstanding-performance, flexible, all-solid-state supercapacitor electrode materials with NiS deposited on discarded biomass carbon, unveiling considerable potential for enhancing energy storage efficiency.

Comparative electrochemical properties of MO (ZrO2, V2O5) based polyaniline nanocomposites for high-performance supercapacitor applications

Due to its distinctive qualities, such as its moderate energy density, extended service life, rapid discharge–charge rates, and superior safety, supercapacitors (SCs) are gaining more and more attention. A zirconium oxide ZrO2 (Zr) and vanadium oxide V2O5 (VO) based PANI nanocomposites, denoted as (ZrP for ZrO2/PANI, and VOP for V2O5/PANI) are fabricated using hydrothermal technique in this research work. Morphological and phase investigations validated the random particle shapes with good crystallinity and purity of the samples. The N2 sorption/desorption isotherm reveals a mesoporous feature of the electrodes and the highest BET surface area (36.5 m2/g) with large electroactive sites, which offers abundant faradaic reactions for charge storage. The I-V characteristics confirm their excellent conduction capabilities as well. When utilized as electrodes for SCs in the three-electrode setup, the VOP composite electrode attains the highest capacitance of 1372 F g−1 at a scan rate of 5 mV s−1 compared with other active electrodes. Besides that, the VOP electrodes offer superior cyclic stability, with a retention rate of 94.28% even after 7000 consecutive charge/discharge cycles. It has been discovered that the in two electrode VOP asymmetric device exhibited remarkable specific capacitance of 651.36 Fg−1 at 5 mV s−1 demonstrating a significant capacitance retention of 87.6% over 6000 cycles. The results suggest that the material could be a good contender for electrode materials in supercapacitors.

Triarylamine-based polyimide COFs for achieving high performance ambipolar multi-color electrochromic energy-storage films

Electrochromic energy storage materials that possess both electrochromic and electrochemical energy-storage properties have attracted significant attention for applications in visual energy-storage, energy-efficient windows, as well as displays. To fulfill their comprehensive applications, electrochromic energy-storage materials require specific characteristics, such as transparency, ambipolarity, multi-color capabilities, and high capacitance. Here, the polyimide covalent-organic framework based on triarylamine (PM-TPI and NT-TPI) COF films were grown successfully on FTO glass through solvothermal polycondensation, and exhibited crystallization, hierarchical porous structures, and ambipolar electrochemical redox activity. Notably, NT-TPI COF film displayed transparent bleached state, ambipolar electrochromism, multi-color (transparent, orange-red, cyan, gray), and high optical contrast. Due to their large specific surface area and efficient electron/ion transport ability, the NT-TPI COF film effectively controlled visible and near-infrared light, achieving optical contrasts of 49.8 % and 70.0 % at 420 and 850 nm, respectively. Moreover, the NT-TPI COF films showed promising electrochemical energy-storage properties and excellent charge–discharge rate performance, with a specific capacitance of 141.0 mAh/g. Additionally, NT-TPI COF/WO3-based ambipolar eclectrochromic energy-storage devices also exhibited high optical contrast from visible to near-infrared regions, and large capacitance. In summary, the NT-TPI COF film effectively combines the electrochromic and electrochemical energy-storage capabilities, making it a promising candidate for electrochromic energy-storage materials with transparency, ambipolarity, high optical contrast, multi-color functionality, and high specific capacitance.

HBN/PVDF‐HFP and BNNS/PVDF‐HFP nanocomposites as flexible and lightweight dielectric capacitors: High energy storage performance via electrically insulating nanoparticles

AbstractAs the energy demand continuously increases, polymer‐based materials have attracted much attention for energy storage systems as dielectric capacitors due to their higher power density and charge–discharge rate than lithium‐ion batteries and supercapacitors. However, it is necessary to increase the energy density of dielectric capacitors. In this context, poly(vinylidene fluoride‐co‐hexafluoropropylene), PVDF‐HFP, matrix nanocomposites are produced by solution casting method reinforced with hexagonal boron nitride (hBN) nanoparticles and silane‐modified boron nitride nanosheets ‐BNNSs‐ (BNNS‐VTS) up to 10 wt.% filler content. The effects of filler content and surface modification of hBN/BNNSs on PVDF‐HFP matrix nanocomposites' microstructure, phase evolution, crystalization behavior, dielectric properties, and energy storage performance are discussed. 4% hBN/PVDF‐HFP nanocomposite demonstrates 641 MV·m−1 of breakdown strength and 23.2 J·cm−3 of discharged energy density due to hexagonal boron nitride's excellent electrical insulating behavior. The achieved values are 3.0 and 10.5 times superior to the values of the neat thin film, respectively, and they are noteworthy among hBN‐ or BNNS‐reinforced PVDF‐based nanocomposites, even in multi‐layered structures. Furthermore, 4% hBN/PVDF‐HFP presents a giant charge–discharge energy efficiency (92%). It is thus demonstrated that hBN/PVDF‐HFP nanocomposites hold a great potential to be used in energy storage applications as flexible and lightweight dielectric capacitors.Highlights PVDF‐HFP matrix nanocomposites for electrical energy storage as flexible dielectric capacitors hBN NPs and silane‐modified BNNSs are reinforced into the matrix by 0–10 wt.%. The effects of filler content and surface modification of hBN/BNNSs are discussed. 4% hBN loading results in 23.2 J·cm−3 energy density and 92% efficiency at 641 MV·m−1 breakdown strength. Those metrics are relatively high in hBN‐ or BNNS‐reinforced PVDF‐based nanocomposites.

(Digital Presentation) In-Situ Growth of CNT and Macroporous ZIF on Bacterial Cellulose for High Frequency Electrochemical Capacitor

High frequency electrochemical capacitors (HF-ECs) represent a class of devices characterized by their high capacitive density and operational capability within the hundreds or kilohertz range. As electronic devices continue to undergo downsizing trends, HF-ECs emerge as promising alternatives to bulky aluminum electrolytic capacitors (AECs), which are constrained by their limited working frequency of approximately 1 Hz and slow charge-discharge rates. The designing of electrodes of HF-ECs combines large surface area for capacitive density along with open porous network to facilitate rapid ion transport. In this study, we synthesized nickel coordinated ZIF-8 (Zeolitic Imidazole Framework-8) cages on bacterial cellulose (BC). The samples underwent rapid carbonization in the presence of dicyandiamide at ~950˚C for 20 minutes, during which the zinc centers inside the MOF cages evaporated forming macroporous structures, while the nickel particles gave rise to carbon nanotube (CNT) growth through tip growth mechanism. The uniform coverage of BC with macroporous ZIF cages reduces the microporous effect, while the CNT growth also imparts higher electronic conductivity via graphitic nitrogen groups. The HF-ECs made with these electrodes and 6M KOH aqueous electrolyte gave a capacitive density of ~3.4 mFcm-2 and a phase angle of -81.3˚. The electrodes were stacked in pairs of 2 and 3 to achieve higher capacitance of 6.3 mFcm-2 and 8.9 mFcm-2 respectively. The HF-ECs were also assembled with 1 M TEABF4 in acetonitrile to show higher working voltage of these electrodes. The device maintained a capacitance just above 3 mFcm-2 and a phase angle over -80˚. The cells show an excellent working capability at higher discharge rates of 100 mAcm-2, where they retained ~70% of the initial capacitance. Figure 1

Improving rate performance of FeC2O4/rGO composites on lithium storage via single-polymerization‐induced electrostatic self‐assembly

Based on the wide interlayer distance for ions diffusion, iron (II) oxalate exhibits excellent lithium storage ability. However, the local deposition of metallic nanoparticles of Fe0 leads to low electrochemical reactivity, which hinders the actual application of FeC2O4 in large current regions (>5C). To solve this problem, a strong cationic polymeric electrolyte, polyelectrolyte diallyl dimethyl ammonium (PDDA), was introduced to construct a [FeC2O4(PDDA)]+ ligand. By single-polymerization‐induced electrostatic self-assembly, the [FeC2O4(PDDA)]+ ligand was combined with the surface-charged rGO to produce a FeC2O4/rGO material. It is proved that the rGO carrier improves the interparticle conductivity, electrochemical activity and structure stability of the iron (II) oxalate particles, ensuring the stability of Li || FeC2O4/rGO battery at a rapid charging rate of 20C (8 A g−1) for more than 500 cycles (with the special capacity of 713 mAh g−1). Compared with FeC2O4 electrode, owning to high reactivity of rGO and continuously activating on the nanoscale Fe metal generated at ∼0.75 V, FeC2O4/rGO shows higher electrochemical activity of conversion reaction in the first 50 cycles and better reversibility in the rate charge–discharge test (the capacity rapidly increased to 1158.8 mAh g−1 after 20C cycles). This work reveals how the structural design of conducting and supporting the carrier can achieve fast charging for iron (II) oxalate lithium-ion batteries.

Binder-dependent electrochemical properties of high entropy oxide anodes for lithium-ion batteries

High entropy oxide (HEO) materials have recently emerged as promising anodes for lithium-ion batteries (LIBs). In this study, we conduct the first comparative analysis to investigate the influence of various electrode binders on electrochemical properties of (CrMnFeNiCu)3O4 HEO anodes. The organic-solvent-soluble polyvinylidene fluoride and water-soluble polyvinyl formamide, sodium carboxymethyl cellulose, sodium alginate, and sodium polyacrylate (NaPAA) binders are examined. Notably, the NaPAA binder leads to a significant enhancement in the HEO performance. The NaPAA coating on (CrMnFeNiCu)3O4 effectively improves the electrode charge-discharge Coulombic efficiency and mitigates the electrode deterioration. Binder adhesion strength and stability toward electrolyte are assessed. The charge-transfer resistance and apparent Li+ diffusion of the HEO electrodes with various binders, accompanied by the post-cycling analyses, are examined. By employing the NaPAA binder, exceptional electrode capacities of 800 and 495 mAh g–1 are attained at charge-discharge rates of 50 and 2000 mA g–1, respectively, without noticeable capacity degradation after 300 cycles. The thermal reactivity of the lithiated electrodes is investigated using differential scanning calorimetry, and the impact of binders on the electrode exothermic onset temperature and total heat released is studied. Our findings provide valuable insights for enhancing the performance and safety of HEO anodes for LIBs.

Relaxation and energy storage properties of NaNb0.98Ta0.02O3 modulated (Na0.5Bi0.5)0.935Sr0.065TiO3 ceramics

Dielectric capacitors with excellent power density and rapid charge-discharge rates have received significant attention in the field of pulsed power. In this study, anti-ferroelectric NaNb0.98Ta0.02O3 was doped into (Na0.5Bi0.5)0.935Sr0.065TiO3 ceramics, resulting in a substantial improvement of the integrated energy storage performance of the ceramics. Multiscale testing confirmed that the ceramic system formed a dense solid solution with a single-phase perovskite structure. Increasing the content of NaNb0.98Ta0.02O3 effectively enhances the relaxation and energy storage properties of the ceramics, while reducing average grain size improves their breakdown field strength, leading to excellent electrical properties at 30 kV/mm field strength when x = 0.2 for this ceramic system - exhibiting recoverable energy storage density Wrec = 7.98 J/cm3 and energy storage efficiency η = 90 %. Furthermore, it demonstrates excellent stability over a wide frequency range (5–90 Hz): Wrec = 7.97 ± 2 % J/cm3, η = 89 ± 1 %; as well as stability over a wide temperature range (30–200 °C): Wrec = 7 ± 2 % J/cm3, η = 89 ± 1 %, along with a rapid charging-discharging rate t0.9 = 0.32 μs. These outstanding properties indicate great prospects for future applications of this ceramic system in the field of energy storage capacitors.