Rechargeable Research Articles

Anode‐Free Solid‐State Rechargeable Batteries: Mechanisms, Challenges, and Design Strategies

Anode‐free solid‐state alkali metal batteries (AFSSAMBs) have emerged as promising high‐performance battery systems, attracting significant scientific interest due to their exceptional safety, high theoretical energy density, and cost‐effectiveness. Recently, extensive research efforts have focused on addressing the key issues impeding their practical deployment, primarily centered around severe dendrite growth, unstable electrolyte‐electrode interface, and low Coulombic efficiency. Despite this progress, a comprehensive framework for the fundamental understanding of AFSSAMBs is still lacking. This paper presents a comprehensive concept, outlining detailed construction, mechanisms, challenges, and strategies of AFSSAMBs. First, the basic configuration and internal mechanisms of AFSSAMBs are summarized. Subsequently, we discuss the existing challenges hindering the cycling lifespan of AFSSAMBs, offering several promising approaches to overcome these obstacles. In the end, insightful perspectives and viewpoints are briefly proposed on the further developments of AFSSAMBs.

Sodium Vanadates for Metal-Ion Batteries: Recent Advances and Perspectives.

Rechargeable metal-ion batteries (MIBs) play a pivotal role in advancing the stable supply of renewable energy by efficiently storing and discharging electrical energy. In recent years, to propel the continuous advancement of MIB technology, numerous studies have concentrated on exploring and innovating electrode materials, aiming to engineer commercial batteries with high energy density, superior power density, and extended cycle life. Notably, sodium vanadates have garnered significant attention in the realm of MIBs owing to their distinctive crystal structures, abundant resource reservoirs, and exceptional electrochemical properties. This paper provides a prompt and comprehensive review of the research landscape for various sodium vanadates (such as NaxV2O5, Na1+ xV3O8, Na2V6O16·xH2O, etc.) in the domain of MIBs over the past five years. It delves into the structural characteristics, electrochemical performances, and energy storage mechanisms of these materials, while also proposing some effective strategies to augment their electrochemical capabilities. Building upon these insights and prevailing research outcomes, this review envisions the future developmental pathways of sodium vanadates for MIBs and aims to reveal the vast potential of sodium vanadates in the emerging energy storage field and provide researchers with clear insights and perspectives for developing optimal sodium vanadate electrodes.

Exploring Hidden Connections: Endophytic System and Flower Meristem Development of Pilostyles berteroi (Apodanthaceae) and Interaction with Its Host Adesmia trijuga (Fabaceae)

Pilostyles, an endoparasitic genus within the Apodanthaceae family, grows inside host stems with flowers and fruits being the only external manifestations. Previous studies of P. berteroi growing on Adesmia trijuga provided limited details of the endophyte and omitted the origin of flowers and sinker structure. This study, using classical methods of optical microscopy applied to the analysis with scanning electron microscopy and confocal laser scanning microscopy, expands the understanding of the P. berteroi/A. trijuga complex. We find that P. berteroi develops isophasically with its host, forming endophytic patches between the host’s secondary phloem cells. The parasitized Adesmia stem’s cambium primarily produces xylem parenchyma, with limited vessel production and halting fiber formation. The radial polarization of endophytic patches led to the formation of floral meristems. Flowers develop endogenously and emerge by the breakthrough of the host stem. Flowers are connected to the host cambium via chimeric sinkers, combining P. berteroi parenchyma and tracheoids with Adesmia vessels. Unlike previous studies that show uniformity among Pilostyles species, our analysis reveals new insights into the structural interaction between P. berteroi and A. trijuga.

Carbon Dots Enabling High-Performances Sodium-Ion Batteries.

Carbon dots (CDs), known for their quantum size, abundant surface functional groups, excellent biocompatibility, and non-toxicity, have emerged as promising candidates for enhancing various advanced rechargeable batteries. Recent research indicates that electrodes based on or modified with CDs in sodium-ion batteries (SIBs) have shown significant improvements in key performance metrics such as Coulombic efficiency, cycle life, and capacity compared to traditional electrodes. Several key impacts of CDs contribute to these enhancements, including increased conductivity due to their conductive graphitized core, rich absorption sites, and excellent dispersity facilitated by abundant surface functional groups. These features accelerate ion transport through interface edges and ion diffusion paths, inhibit electrode material dissolution, buffer electrode material volume expansion, ensure electrode uniformity and stability, and promote the electrochemical reaction process between the electrode and electrolyte. This review summarizes recent developments, challenges, and opportunities in leveraging CDs as additives in SIBs, focusing on their impact on electrolyte properties, electrode materials, and overall battery performance. It provides a comprehensive understanding of the potential of CDs to significantly advance SIB technology.

Na ions doped Fe2VO4 cathode for high performance aqueous zinc‐ion batteries

Aqueous zinc ion batteries are thought to be a new generation of secondary batteries that will replace lithium ion batteries due to their great safety and inexpensive cost. In the cathode materials of aqueous zinc ion batteries with long life and high capacity, abundant active sites and crystal structure stability play an important role. In the present work, the strategy of Na+ intercalation of Fe2VO4 (FVO) is proposed, aiming at the insertion of Na+, which not only enriches the active sites, but also sodium and iron ions act as guest species with the negatively charged VOx lattice to provide strong electrostatic attraction to stabilize the lamellar structure. In terms of electrochemical performance, the discharge specific capacity is 370 mAh g‐1 at a current density of 0.1 A g‐1, and when the current density is arising 5 A g‐1, the specific capacity also reaches 200 mAh g‐1 after cycling 2000 with a capacity retention of 99%, which is better than the electrochemical performance of Fe2VO4 (FVO) alone at 50 mAh g‐1. The superior electrochemical performance proves that FVO‐Na is an ideal cathode material for zinc ion batteries.

In Situ Construction of Perovskite Pr0.5Ba0.5Mn0.8Co0.1Ru0.1O2.5+δ/CoRu Nanoparticles with Co-N-C Composite Enabling Efficient Bifunctional Electrocatalyst for Zinc-Air Batteries.

Bifunctional catalysts for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) are essential components of rechargeable zinc-air batteries. In this study, we synthesized a Pr0.5Ba0.5Mn0.8Co0.1Ru0.1O2.5+δ (PBMCRO) perovskite composite with in situ exsolved CoRu nanoparticles and Co-N-C, functioning as an efficient bifunctional electrocatalyst for zinc-air batteries. The in situ exsolution of CoRu nanoparticles from the perovskite oxide was facilitated by the reducing action of 2-methylimidazole (2-MIM). Concurrently, Co-N-C was used to decorate PBMCRO, forming a novel bifunctional composite electrode of Co-N-C-PBMCRO. The incorporation of CoRu nanoparticles introduces a significant number of electrochemically active oxygen vacancies in the perovskite matrix, enhancing ORR and OER performance. Additionally, the Co-N-C synergistically improves electrochemical activity while preserving the structural stability of the perovskite oxide. The prepared Co-N-C-PBMCRO catalyst demonstrates significantly enhanced bifunctional performance compared to the undecorated pristine perovskite Pr0.5Ba0.5MnO3-δ (PBMO). The zinc-air battery with Co-N-C-PBMCRO catalyst achieve a peak power density of approximately 90 mW/cm2 and exhibit remarkable cycling stability for 788 h. This study presents a novel and effective strategy to enhance the catalytic performance of perovskite-based air electrodes for rechargeable metal-air batteries.

A non-isolated converter of switching current stress in DC-DC converter for integrating PV and battery storage system

ABSTRACT High-gain DC-DC converters have seen significant adoption in renewable energy systems like Photovoltaic (PV), Fuel Cells (FC), and other systems. However, their effectiveness is increasingly tied to the availability of renewable resources. As Renewable Energy Sources (RES) typically generate electricity at low voltage levels, integrating high-gain DC-DC converters with RES is crucial for optimal performance. This paper introduces an innovative DC-DC converter design that achieves high gain and is specifically able to integrate smoothly with RES like PV systems and battery storage. The innovation of the proposed converter lies in its integration of conventional boost and buck-boost converters, enabling a high voltage gain while minimizing output voltage ripple and reducing switch current stress. Additionally, its unidirectional power transfer port allows efficient energy flow from solar PV or battery sources to the load, making it highly adaptable for managing fluctuating energy sources, a feature that distinguishes it from current modern converters. Its design simplifies architecture by combining traditional converter types, reducing the number of components, which leads to cost savings, lower weight, and improved reliability. Additionally, the design minimizes output voltage ripple and reduces switching current stress, enhancing the converter’s durability under variable operating conditions. The converter’s performance is evaluated through simulation and experimental studies, demonstrating a 96.3% efficiency and 5.5 times of voltage gain. The converter’s feasibility and effectiveness are validated under dynamic scenarios with varying solar irradiation, making it an ideal solution for clean energy generation systems, including hybrid energy generation setups. The proposed converter topology offers an auspicious solution for high-gain DC-DC conversion in renewable energy systems.

The Potential Role of PeMAP65-18 in Secondary Cell Wall Formation in Moso Bamboo

Microtubule-associated proteins (MAPs) play a pivotal role in the assembly and stabilization of microtubules, which are essential for plant cell growth, development, and morphogenesis. A class of plant-specific MAPs, MAP65, plays largely unexplored roles in moso bamboo (Phyllostachys edulis). This study identified 19 PeMAP65 genes in moso bamboo, systematically examining their phylogenetic relationships, conserved motifs, gene structures, collinearity, and cis-acting elements. Analysis of gene expression indicated that PeMAP65s exhibit tissue-specific expression patterns. Functional differentiation was investigated among the members of different PeMAP65 subfamilies according to their expression patterns in different development stages of bamboo shoots. The expression of PeMAP65-18 was positively correlated with the expression of genes involved in secondary cell wall (SCW) biosynthesis. Y1H and Dual-LUC assays demonstrated that the transcription of PeMAP65-18 was upregulated by PeMYB46, a key transcription factor of SCW biosynthesis. The result of subcellular localization showed that PeMAP65-18 was located in cortical microtubules. We speculate that PeMAP65-18 may play a crucial role in the SCW deposition of moso bamboo. This comprehensive analysis of the MAP65 family offers novel insights into the roles of PeMAP65s in moso bamboo, particularly in relation to the formation of SCWs.

The Development and Prospect of Stable Polyanion Compound Cathodes in LIBs and Promising Complementers.

Cathode materials are usually the key to determining battery capacity, suitable cathode materials are an important prerequisite to meet the needs of large-scale energy storage systems in the future. Polyanionic compounds have significant advantages in metal ion storage, such as high operating voltage, excellent structural stability, safety, low cost, and environmental friendliness, and can be excellent cathode options for rechargeable metal-ion batteries. Although some polyanionic compounds have been commercialized, there are still some shortcomings in electronic conductivity, reversible specific capacity, and rate performance, which obviously limits the development of polyanionic compound cathodes in large-scale energy storage systems. Up to now, many strategies including structural design, ion doping, surface coating, and electrolyte optimization have been explored to improve the above defects. Based on the above contents, this paper briefly reviews the research progress and optimization strategies of typical polyanionic compound cathodes in the fields of lithium-ion batteries (LIBs) and other promising metal ion batteries (sodium ion batteries (SIBs), potassium ion batteries (PIBs), magnesium ion batteries (MIBs), calcium ion batteries (CIBs), zinc ion batteries (ZIBs), aluminum ion batteries (AIBs), etc.), aiming to provide a valuable reference for accelerating the commercial application of polyanionic compound cathodes in rechargeable battery systems.

FUZZY LOGIC-BASED POWER MANAGEMENT IN GRID-CONNECTED SOLAR ENERGY SYSTEMS

With the ever-increasing application of photovoltaic systems on the power grid, energy flow management and grid stability have become a key factor, especially under varying conditions like variable cloud cover and fluctuating load demands. The paper looks forward to proposing a fuzzy logic approach to the management of energy regarding a solar energy system connected to a grid, aiming at obtaining an optimised power distribution among PV generation, the grid, and battery storage. The proposed system will be driven by five input parameters, PV value, grid availability, load demand, battery state of charge, and tariff rate, to regulate the energy flow activity within different scenarios. The simulation results developed in the MATLAB Simulink environment proved the effectiveness of the applied controller in maintaining energy stability and fulfilling the requirements of a load within seven case studies for a 24-hour duration. The work points out the potential of fuzzy logic, besides reliability, in enhancing the efficiency of various renewable energy systems integrated with conventional energy supply grids.<p> </p><p><strong> Article visualizations:</strong></p><p><img src="/-counters-/soc/0799/a.php" alt="Hit counter" /></p>

Redox Activity of Co Species in the Active Sites of CoNx/CoOx Facilitates Oxygen Electrocatalysis for Zn-Air Batteries.

Developing efficient bifunctional oxygen electrocatalysts is crucial for enhancing the performance of rechargeable Zn-air batteries (ZABs). In this study, cobalt/cobalt oxides embedded in N-doped carbon nanofibers (Co/CoOx/NCNFs) were synthesized through a combination of electrospinning and annealing processes. The resulting Co/CoOx/NCNFs catalysts feature abundant CoNx and CoOx active species, leveraging the large specific surface area of nanofibers to facilitate oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). The optimized Co/CoOx/NCNFs-0.1 achieved a half-wave potential (vs. RHE) of 0.82 V and required only 429 mV to reach 10 mA cm-2 in a typical three-electrode system with 0.1 M KOH using an electrochemical workstation equipped with a pine instruments rotator, outperforming the Pt/C+RuO2. The assembled ZABs exhibited high specific capacity (771 mAh gZn -1), substantial power density (981.6 mWh gZn -1), and long-term stability (>325 h). In situ Raman spectroscopy confirmed that the electrocatalytic processes involve the redox activity of Co (II and III) species derived from abundant CoNx and CoOx, elaborating the origin of the catalysts' exceptional oxygen electrocatalysis performance. This work not only presents a straightforward and effective approach for producing bifunctional oxygen electrocatalysts in ZABs but also sheds light on the catalytic mechanisms underlying ORR and OER for CoNx/CoOx-based oxygen electrocatalysts.

Helmholtz Plane Regulation Empowers PF6− Permselectivity Towards High Coulombic Efficiency Dual Ion Battery of 5.5 V

AbstractHigh‐voltage dual ion battery (DIB) is promising for stationary energy storage applications owing to its cost‐effectiveness, which has been a hot topic of research in rechargeable battery fields. However, it still suffers from rapid battery failure caused by the severe solvent co‐intercalation and electrolyte oxidation. To address these bottlenecks, herein a functional electrolyte additive hexafluoroglutaric anhydride (HFGA) is presented based on a Helmholtz plane regulation strategy. It is demonstrated that the HFGA can precisely enter into the Helmholtz plane and positively regulate anion solvation behaviors near the graphite electrode surface owing to its considerable H−F affinity with ethyl methyl carbonate (EMC), thus alleviating EMC‐related co‐intercalation and oxidation decomposition during DIB charging. Meanwhile, HFGA can copolymerize with the presence of PF5 at the Helmholtz plane to participate in forming a CF2‐rich CEI layer with excellent PF6− permselectivity, conducive to achieving PF6− de‐solvation and simultaneously suppressing electrolyte oxidation decomposition. By virtue of such beneficial effects, the graphite cathode enables a 5.5 V DIB with a prominent capacity retention of 92 % and a high average Coulombic efficiency exceeding 99 % within 2000 cycles at 5 C, demonstrating significantly enhanced electrochemical reversibility. The Helmholtz plane regulation strategy marks a milestone in advancing DIB technologies.

Synergistic Interaction of Strongly Polar Zinc Selenide and Highly Conductive Carbon Nanoframeworks Accelerates Redox Kinetics of Polysulfides.

Lithium-sulfur batteries (LSBs) have become strong competitors in secondary battery systems because of their superior theoretical capacity and energy density. However, due to the serious shuttle effect of soluble long-chain lithium polysulfides (LiPSs) and the slow solid-solid reaction kinetics, LSBs face some specific challenges, such as a short cycle life and low rate performance. The introduction of selenide/carbon composites derived from zeolite imidazolate frameworks (ZIFs) into separator coatings is a direct and effective solution to the aforementioned problems. Here, a zinc selenide/carbon catalyst material (ZnSe@C) was constructed and employed to modify commercial polypropylene (PP) separators to accelerate the conversion of intermediates. The highly polar ZnSe effectively fixes the active material on the cathode side by transferring electrons between elements with LiPSs and improves the utilization rate of sulfur. Concurrently, the highly conductive carbon nanoskeleton generated following the pyrolysis of ZIF-8 ensures the rapid transfer of charges during the catalytic reaction. The prepared ZnSe@C has a large specific surface area (250.07 m2 g-1) and mesoporous ratio (78.03%), which not only enhances adsorption and catalysis but also promotes the penetration of the electrolyte and the transport of Li+. Based on this, ZnSe@C/PP separator cells exhibit a low average capacity decay rate of 0.051% per cycle after 500 cycles at 1 C.

Helmholtz Plane Regulation Empowers PF6 - Permselectivity Towards High Coulombic Efficiency Dual Ion Battery of 5.5 V.

High-voltage dual ion battery (DIB) is promising for stationary energy storage applications owing to its cost-effectiveness, which has been a hot topic of research in rechargeable battery fields. However, it still suffers from rapid battery failure caused by the severe solvent co-intercalation and electrolyte oxidation. To address these bottlenecks, herein a functional electrolyte additive hexafluoroglutaric anhydride (HFGA) is presented based on a Helmholtz plane regulation strategy. It is demonstrated that the HFGA can precisely enter into the Helmholtz plane and positively regulate anion solvation behaviors near the graphite electrode surface owing to its considerable H-F affinity with ethyl methyl carbonate (EMC), thus alleviating EMC-related co-intercalation and oxidation decomposition during DIB charging. Meanwhile, HFGA can copolymerize with the presence of PF5 at the Helmholtz plane to participate in forming a CF2-rich CEI layer with excellent PF6 - permselectivity, conducive to achieving PF6 - de-solvation and simultaneously suppressing electrolyte oxidation decomposition. By virtue of such beneficial effects, the graphite cathode enables a 5.5 V DIB with a prominent capacity retention of 92 % and a high average Coulombic efficiency exceeding 99 % within 2000 cycles at 5 C, demonstrating significantly enhanced electrochemical reversibility. The Helmholtz plane regulation strategy marks a milestone in advancing DIB technologies.

A microscale soft lithium-ion battery for tissue stimulation

AbstractAdvances in the development of tiny devices with sizes below a few cubic millimeters require a corresponding decrease in the volume of driving power sources. To be minimally invasive, prospective power sources in biomedical devices must be fabricated from soft materials. Previous endeavors with droplet-based devices have produced promising miniature power sources; however, a droplet-based rechargeable battery has remained out of reach. Here we report a microscale soft flexible lithium-ion droplet battery (LiDB) based on the lipid-supported assembly of droplets constructed from a biocompatible silk hydrogel. Capabilities such as triggerable activation, biocompatibility and biodegradability and high capacity are demonstrated. We have used the LiDB to power the electrophoretic translocation of charged molecules between synthetic cells and to mediate the defibrillation and pacing of ex vivo mouse hearts. By the inclusion of magnetic particles to enable propulsion, the LiDB can function as a mobile energy courier. Our tiny versatile battery will thereby enable a variety of biomedical applications.

Feature selection and data‐driven model for predicting the remaining useful life of lithium‐ion batteries

AbstractTo ensure long and reliable operation of lithium‐ion battery storage workstations, accurate, fast, and stable lifetime prediction is crucial. However, due to the complex and interrelated ageing mechanisms of Li‐ion batteries, using physical model‐based methods for accurate description is challenging. Therefore, building data‐driven models based on direct measurement data (voltage, current, capacity, etc.) during battery operation may be a more effective approach. This paper employs a time series analysis of discharge capacity/voltage curves to perform feature predication. The goal is to predict the state of health using a short‐term model and the remaining useful life of batteries using a long‐term iterative model. The validity of this method is verified using the open‐source MIT battery dataset. Comparisons with models reported in the literature demonstrate that this method is generalisable and ensures accuracy across a wider range of predictions.

An Organic Small Molecule Electrode with Intermolecular Intercalation and Synergistic Effects for High‐Rate Alkali Metal‐Ion Batteries

AbstractDesignable molecular structures, unique ion‐coordination charge storage mechanisms, and resource sustainability enable organic electrode materials to become potential candidates for alkali metal‐ion batteries (AMIBs). Herein, integrating the excellent π–π stacking ability of Hexaazatriphenylene units and strong electron‐withdrawing properties of cyano (C≡N) groups into one moleuce, a π‐conjugated organic compound 1,4,5,8,9,11‐Hexaazatriphenylenehexacarbonitrile (HAT‐CN) is synthesized and systematically investigated as electrodes in Li/Na/K‐ion batteries. Explored by mechanism characterizations and density functional theory calculations, HAT‐CN can provide nine redox‐active sites for Na/K‐ions to intercalate/de‐intercalate, among which six Na/K‐ions are distributed evenly to both sides of conjugated skeletons through intermolecular intercalation and three Na/K‐ions are stored with the synergistic effect of C≡N groups. Employing HAT‐CN as electrodes, AMIBs are found to exhibit high reversible capacities, excellent rate capabilities, and stable cycle performances. After 100 cycles at the current density of 100 mA g−1, Na‐ion batteries present 415.6 mAh g−1 with a capacity fading rate of 1.2% per cycle. Meanwhile, K‐ion batteries maintain 345 mAh g−1 with a coulombic efficiency ≈100%. Li‐ion batteries display superlithiation performances with ultra‐high reversible capacity. This work emphasizes the necessity of comprehensively studying the electrochemical performance of organic electrodes in different secondary battery systems and is conducive to maximizing electrode functionality.

Application of an Optimal Fractional-Order Controller for a Standalone (Wind/Photovoltaic) Microgrid Utilizing Hybrid Storage (Battery/Ultracapacitor) System

Nowadays, standalone microgrids that make use of renewable energy sources have gained great interest. They provide a viable solution for rural electrification and decrease the burden on the utility grid. However, because standalone microgrids are nonlinear and time-varying, controlling and managing their energy can be difficult. A fractional-order proportional integral (FOPI) controller was proposed in this study to enhance a standalone microgrid’s energy management and performance. An ultra-capacitor (UC) and a battery, called a hybrid energy storage scheme, were employed as the microgrid’s energy storage system. The microgrid was primarily powered by solar and wind power. To achieve optimal performance, the FOPI’s parameters were ideally generated using the gorilla troop optimization (GTO) technique. The FOPI controller’s performance was contrasted with a conventional PI controller in terms of variations in load power, wind speed, and solar insolation. The microgrid was modeled and simulated using MATLAB/Simulink software R2023a 23.1. The results indicate that, in comparison to the traditional PI controller, the proposed FOPI controller significantly improved the microgrid’s transient performance. The load voltage and frequency were maintained constant against the least amount of disturbance despite variations in wind speed, photovoltaic intensity, and load power. In contrast, the storage battery precisely stores and releases energy to counteract variations in wind and photovoltaic power. The outcomes validate that in the presence of the UC, the microgrid performance is improved. However, the improvement is very close to that gained when using the proposed controller without UC. Hence, the proposed controller can reduce the cost, weight, and space of the system. Moreover, a Hardware-in-the-Loop (HIL) emulator was implemented using a C2000™ microcontroller LaunchPad™ TMS320F28379D kit (Texas Instruments, Dallas, TX, USA) to evaluate the proposed system and validate the simulation results.

Nanozyme Hydrogels Promote Nerve Regeneration in Spinal Cord Injury by Reducing Oxidative Stress.

Inhibiting secondary cell death and promoting neuronal regeneration are critical for nerve repair after spinal cord injury (SCI). The excessive accumulation of reactive oxygen species (ROS) after SCI causes cell death and induces apoptosis. These reactions further increase the level of ROS production, leading to a vicious cycle of spinal cord tissue damage. Therefore, intervention targeting ROS is a potential therapeutic approach to improve the recovery of locomotor function after SCI. In this study, we designed and synthesized a nanozyme hydrogel delivery system loaded with multiple drugs, LA/Me/Se NPs-h. LA/Me/Se NPs-h exhibited a satisfactory size distribution and excellent stability, enhancing the bioavailability of therapeutic drugs. Moreover, we explored the antioxidant and protective effects of LA/Me/Se NPs-h against oxidative stress-induced cell damage caused by ROS production after SCI in vitro. In the mice SCI model, the Basso mouse scale and gait analysis showed that LA/Me/Se NPs-h significantly promoted the recovery of locomotor function after SCI. The histological and immunofluorescence results of the injury site revealed that LA/Me/Se NPs-h upregulated the expression of GFAP, NF-200, and superoxide dismutase in spinal cord lesion, reduced caspase-3 expression, improved spinal cord continuity, reduced lesion cavity, and inhibited the axonal demyelination. Consequently, LA/Me/Se NPs-h increased the activity of antioxidant enzymes and reduced neuronal apoptosis by reducing oxidative stress and ultimately promoted nerve regeneration. Taken together, this study demonstrated promising nanozyme hydrogels and provided an effective therapeutic strategy for SCI and other ROS-related diseases.

FeCo Bimetallic ZIF Derivatives decorated with CoFe-LDH to Promote Bifunctional Oxygen Electrocatalysis Activation.

Reasonably screening the targeted oxygen reduction reaction (ORR)/oxygen evolution reaction (OER) constituents and constructing high-efficiency and stabilized ORR/OER bifunctional electrocatalysts are pivotal for the advancement of rechargeable zinc-air batteries (ZABs). Here, CoFe layered double hydroxide (CoFe-LDH) nanosheets are deposited on nitrogen-doped graphite-carbon polyhedra with FeCo alloy nanoparticles (FeCo/LDH-NGCP). Due to the synergic effect between FeCo-NGCP, CoFe-LDH and FeCo/LDH-NGCP, the electrocatalyst with the abundant and accessible active sites can provide good charge/mass transfer, and thus shows wonderful ORR and OER bifunctional electrocatalytic performance. In ORR tests, FeCo/LDH-NGCP catalyst displays larger half-wave potential (E1/2, 0.89 V vs. 0.85 V), higher limiting current density (JL, 5.91 mA/cm2 vs. 5.14 mA/cm2) and better stability than commercial Pt/C. As for OER, FeCo/LDH-NGCP possesses a smaller overpotential (η) of 299.6 mV at a current density of 10 mA/cm2 and more durable stability than commercial RuO2 (330.6 mV). Furthermore, in ZAB tests, the cycling stability of ZAB-FeCo/LDH-NGCP (over 470 h) outperforms the ZAB-Pt/C+RuO2 (92 h) with commercial electrocatalyst (Pt/C+RuO2). Therefore, the FeCo/LDH-NGCP catalyst offers a new perspective to construct ZABs bifunctional catalysts and their commercial application in ZABs.