Search Results (462)

The O3-type layered oxide materials have the advantage of high specific capacity, which makes them more competitive in the practical application of cathode materials for sodium-ion batteries (SIBs). However, the existing reported O3-type layered oxide materials still have a complex irreversible phase transition phenomenon, and the cycle life of batteries needs, with these materials, to be further improved to meet the requirements. Herein, we performed structural characterization and electrochemical performance tests on O3-NaNi_0.6−xFe_0.25Mn_0.15Mg_xO₂ (x = 0, 0.025, 0.05, and 0.075, denoted as NFM, NFM-2.5Mg, NFM-5.0Mg, and NFM-7.5Mg). The optimized NFM-2.5Mg has the largest sodium layer spacing, which can effectively enhance the transmission rate of sodium ions. Therefore, the reversible specific capacity can reach approximately 148.1 mAh g⁻¹ at 0.2C, and it can even achieve a capacity retention of 85.4% after 100 cycles at 1C, demonstrating excellent cycle stability. Moreover, at a low temperature of 0 °C, it also can keep capacity retention of 86.6% after 150 cycles at 1C. This study provides a view on the cycling performance improvement of sodium-ion layered oxide cathodes with a high theoretical specific capacity. Full article

The corrosion behavior and electrochemical performance of Mg-La-Zr and Mg-La alloys were studied. Microstructural observation indicated that the trace alloying of Zr refined the grain size of Mg-La alloy, which improved the discharge activity of Mg-La alloys. At the same time, the addition of Zr led to a transformation of the second-phase distribution from intracrystalline to grain boundary central distribution. This change inhibited the self-corrosion of the alloy during discharge and improved the anode utilization efficiency. Therefore, an air battery based on a Mg-La-Zr alloy anode with a unique microstructure demonstrated a high discharge performance. In this paper, the relationship between the microstructure and anodic properties of Mg-La-Zr alloy are systematically elucidated. Full article

The existing standalone microgrids (MGs) require good energy management systems (EMSs) to respond to energy needs. The EMS presented in this paper is used for an MG based on PV and wind energy sources. The energy storage system is implemented using three packs of batteries. Power smoothing is carried out via the introduction of supercapacitors (SCs) in parallel to the loads and sources. The distribution of energy of the presented MG is focused on the multi-agent system (MAS) using Fuzzy Logic Supervisor control. The MAS is used in order to leverage autonomous and interacting agents to optimize operations and achieve system objectives. To reduce the stress on batteries and avoid damaging all the batteries together by the charge and discharge cycles, one pack of batteries can usually be used. When this pack of batteries is fully discharged and there is a need for energy, it can be taken from another pack of batteries. The same analysis applies to the charge; when batteries of the first pack are fully charged and there is a surplus of energy, it can be stored in other packs of batteries. Two simulation results are used to demonstrate the efficiency of the EMS control used. These simulation tests are proposed with and without SCs. Full article

The broad-spectrum insect growth regulator (IGR) and insecticide 2-((1-(4-Phenoxyphenoxy)propan-2-yl)oxy)pyridine (MPEP; also known as pyriproxyfen) is increasingly being used to address public health programs for vector control, initiated by the spread of Zika virus in 2015–2016. While considered relatively safe for humans under normal conditions, limited toxicology data are available. Current studies were undertaken to address the data gap regarding potential immunotoxicity of MPEP, with particular emphasis on host resistance to viral infection. Hsd:Harlan Sprague Dawley SD^® rats were treated for 28 days by oral gavage with doses of 0, 62.5, 125, 250 or 500 mg/kg/day of MPEP in corn oil. There was a dose-dependent increase in liver weights which is consistent with the liver playing a dominant role in MPEP metabolism. However, no histological correlates were observed. Following treatment, rats were subjected to a battery of immune tests as well as an established rat model of influenza virus infection to provide a comprehensive assessment of immune function and host resistance. While several of the immune tests showed minor exposure-related changes, evidenced by negative dose–response trends, most did not show significant differences in any of the MPEP treatment groups relative to vehicle control. Most notable was a negative trend in pulmonary mononuclear cell phagocytosis with increases in dose of MPEP. There was also a positive trend in early humoral immune response (5 days after immunization) to keyhole limpet hemocyanin (KLH) as evidenced by increased serum anti-KLH IgM antibodies which was followed later (14 days following immunization) by decreasing trends in anti-KLH IgM and IgG antibody levels. However, MPEP treatment had no effect on the ability of rats to clear the influenza virus nor the T-dependent IgM and IgG antibody response to the virus. The lack of effects of MPEP on host resistance to influenza suggests the immune effects were minimal and unlikely to present a hazard with respect to susceptibility to respiratory viral infection. Full article

The cointercalation of solvated Mg²⁺ ions into graphite has typically been considered challenging because of concerns regarding the instability of the electrolyte and the potential for structural degradation. However, recent developments in electrolyte design suggest that this process may be reversible under appropriate conditions. In this study, the interfacial behavior of graphite in a magnesium-ion system was investigated using in situ electrochemical atomic force microscopy. Electrochemical tests in a triglyme-based electrolyte revealed a reversible capacity of 158 mAh g⁻¹, attributed to the insertion of triglyme-solvated Mg²⁺ ions. Real-time surface imaging of highly oriented pyrolytic graphite revealed the formation of a passivating surface film during the initial cycle, along with nanoscale hill-like (~1 nm) and blister-like (~5 nm) structures, which were partially reversible and showed good correlation with the redox peaks observed in the cyclic voltammetry experiments, suggesting that the surface film enables Mg²⁺ transport while mitigating electrolyte decomposition. These findings demonstrate that stable co-intercalation of solvated Mg²⁺ ions is achievable in the early cycles in graphite and highlight the importance of interfacial engineering and solvation structures in the development of magnesium-ion batteries. Full article

Asbolane is a secondary source of cobalt (Co) and manganese (Mn), essential for battery and alloy production. Enhancing the utilization of low-grade ores, typically containing ~1.2% Co and 14.7% Mn, is vital for conserving high-grade resources. However, fine grinding for such ores presents challenges for conventional gravity separation. This study investigates the effectiveness of the Multi-Gravity Separator (MGS) in processing finely disseminated asbolane ore from Agios Ioannis, Greece. The study was conducted at the Mineral Processing Laboratory of UPC/Bases Manresa. Two size fractions, D₈₀ (−100 +50 µm and −50 µm), were tested under varying drum speeds, tilt angles, and wash water flows. Response surface methodology (RSM) was implemented using Python-optimized (version 3.15) process parameters. The results demonstrate that a concentrate with 2.6% Co and 32.5% Mn can be obtained, achieving 82.1% Co recovery. Independent and multi-objective optimizations confirm MGS as a viable method for recovering Co and Mn from complex low-grade ores, with reduced overgrinding-related energy losses essential for production. The study aimed to implement and enhance low-grade asbolane ore from a feed containing 2.6% Co and 32.5% Mn. Variables were optimized with a multi-objective target, demonstrating their effectiveness. Full article

Trigeminal neuralgia is a chronic pain disorder due to neuronal damage. The present study was designed to investigate the effect of 7,8-dimethoxy coumarin (DMC) in a rat model of trigeminal neuralgia. The neuropathic pain was induced by the single endoneural injection of tumor necrosis factor-alpha (TNF-α; 0.1 μL: stock 10 pg/mL) in the rat trigeminal nerve. The DMC (100 and 200 mg/kg) and carbamazepine (100 mg/kg) were administered orally for 10 consecutive days from the 5th day of TNF-α injection. The battery of behavioral tests, i.e., acetone drop and Von Frey filament test, was performed to assess the degree of thermal and mechanical allodynia on 0, 1st, 7th, and 14th days. In addition, the biochemical tests, i.e., total protein, thiobarbituric acid reactive substances (TBARS), reduced glutathione (GSH), and TNF-α, were also performed in trigeminal nerve tissue. Furthermore, TNF-α-induced neuronal histopathological changes were also evaluated by the eosin and hematoxylin staining method. The administration of DMC was shown to demonstrate the significant (p < 0.05) reversal of TNF-α-induced percentage reduction of thermal and mechanical sensitivity, along with a rise in TBARS and TNF-α and a decrease in GSH levels. Further, DMC also attenuates the histopathological changes. It may be concluded that DMC may be a potential therapeutic agent for the management of trigeminal neuralgia disorders. Full article

This study explores the development of aluminum-doped MgV₂O₄ spinel cathodes for aqueous zinc-ion batteries (AZIBs), addressing the challenges of poor Zn²⁺ ion diffusion and structural instability. Al³⁺ ions were pre-inserted into the spinel structure using a sol-gel method, which enhanced the material’s structural stability and electrical conductivity. The doping of Al³⁺ mitigates the electrostatic interactions between Zn²⁺ ions and the cathode, thereby improving ion diffusion and facilitating efficient charge/discharge processes. While pseudocapacitive behavior plays a dominant role in fast charge storage, the diffusion of Zn²⁺ within the bulk material remains crucial for long-term performance and stability. Our findings demonstrate that Al-MgV₂O₄ exhibits enhanced Zn²⁺ diffusion kinetics and robust structural integrity under high-rate cycling conditions, contributing to its high electrochemical performance. The Al-MgVO cathode retains a capacity of 254.3 mAh g⁻¹ at a high current density of 10 A g⁻¹ after 1000 cycles (93.6% retention), and 186.8 mAh g⁻¹ at 20 A g⁻¹ after 2000 cycles (90.2% retention). These improvements, driven by enhanced bulk diffusion and the stabilization of the crystal framework through Al³⁺ doping, make it a promising candidate for high-rate energy storage applications. Full article

The need for electrical energy is dramatically increasing, pushing researchers and industrial communities towards the development and improvement of microgrids (MGs). It also encourages the use of renewable energies to benefit from available sources. Thereby, the implementation of a photovoltaic (PV) system with a hybrid energy storage system (HESS) can create a standalone MG. This paper presents an MG that uses photovoltaic energy as a principal source. An HESS is required, combining batteries and supercapacitors. This MG responds “insure” both alternating current (AC) and direct current (DC) loads. The batteries and supercapacitors have separate parallel connections to the DC bus through bidirectional converters. The DC loads are directly connected to the DC bus where the AC loads use a DC-AC inverter. A control strategy is implemented to manage the fluctuation of solar irradiation and the load variation. This strategy was implemented with a new logic control based on Boolean analysis. The logic analysis was implemented for analyzing binary data by using Boolean functions (‘0’ or ‘1’). The methodology presented in this paper reduces the stress and the faults of analyzing a flowchart and does not require a large concentration. It is used in this paper in order to simplify the control of the EMS. It permits the flowchart to be translated to a real application. This analysis is based on logic functions: “Or” corresponds to the addition and “And” corresponds to the multiplication. The simulation tests were executed at T_au  =  6 s of the low-pass filter and conducted in 60 s. The DC bus voltage was 400 V. It demonstrates that the proposed management strategy can respond to the AC and DC loads. Full article

Germanium/tin-containing silicon oxide [SiO–(GeO/SnO)] nanoclusters have been designed with different Si/Ge/Sn particles and characterized as electrodes for magnesium-ion batteries (MIBs) due to forming MgBe [SiO–GeO], MgBe [SiO–SnO], MgCa [SiO–GeO], and MgCa [SiO–SnO] complexes. In this work, alkaline earth metals of magnesium (Mg), beryllium (Be), and calcium (Ca) have been studied in hybrid Mg-, Be-, and Ca-ion batteries. An expanded investigation on H capture by MgBe [SiO–(GeO/SnO)] or MgCa [SiO–(GeO/SnO)] complexes was probed using computational approaches due to density state analysis of charge density differences (CDD), total density of states (TDOS), and electron localization function (ELF) for hydrogenated hybrid clusters of MgBe [SiO–GeO], MgBe [SiO–SnO], MgCa [SiO–GeO], and MgCa [SiO–SnO]. Replacing Si by Ge/Sn content can increase battery capacity through MgBe [SiO–GeO], MgBe [SiO–SnO], MgCa [SiO–GeO], and MgCa [SiO–SnO] nanoclusters for hydrogen adsorption processes and could improve the rate performances by enhancing electrical conductivity. A small portion of Mg, Be, or Ca entering the Si–Ge or Si–Sn layer to replace the alkaline earth metal sites could improve the structural stability of the electrode material at high multiplicity, thereby improving the capacity retention rate. In fact, the MgBe [SiO–GeO] remarks a small enhancement in charge transfer before and after hydrogen adsorption, confirming the good structural stability. In addition, [SiO–(GeO/SnO)] anode material could augment the capacity owing to higher surface capacitive impacts. Full article

The global energy shortage and the gradual depletion of lithium resources have become increasingly prominent. Improving the energy density of lithium-based secondary batteries and developing other high-performance alkali-metal secondary batteries have become the research focus. In this study, two-dimensional (2D) hexagonal metal borides (h-MBenes) are investigated as ordered alkali metal adsorption substrates for alkali-metal-based battery anode materials using density functional theory (DFT). Twelve thermodynamically stable h-MBenes are screened out from thirty-three structures, and their excellent stability and metallic electronic characteristics are confirmed. The ordered multilayered growth in alkali metal adsorption is found to depend on two factors: low lattice mismatching and dynamic matching of the work function. In particular, Mg/Al/V-based h-MBenes exhibit excellent lithium lattice matching (<3.35% mismatch), enabling layer-by-layer hexagonal (001) Li growth for ≥5 layers. They have ultrahigh lithium capacities (2170–3818 mAh·g⁻¹), low migration barriers (0.01–0.05 eV), and low voltages (0.003–0.714 V). Mg/Y-based h-MBenes enable three Na layers’ adsorption with a capacity of 1717/605 mAh·g⁻¹, and Al₂B₂ achieves a 472 mAh·g⁻¹ potassium storage capacity, respectively. Due to the orderly multilayered growth mechanism, Mg/Al/V-based h-MBenes show great potential as high-safety and ultrahigh-capacity alkali-metal battery anode materials. Full article

The removal of heavy metals from industrial wastewater remains a major environmental challenge, demanding efficient, sustainable solutions. This study explores the combined use of Chlorella vulgaris and amine-functionalized magnesium ferrite (MgFe₂O₄-NH₂) nanoparticles to remove cobalt ions from battery effluents. The research aims to explore the capacity of C. vulgaris to adsorb heavy metals, followed by their separation using magnetic nanoparticles. Cobalt adsorption by C. vulgaris was facilitated through the interaction of metal ions on the cell wall, achieving a removal efficiency of 96.44% within 30 min, which increased to 98.78% over 10 h. Amine-functionalized MgFe₂O₄ nanoparticles, synthesized and characterized using HRTEM, FTIR, and VSM, displayed high surface reactivity due to the presence of -NH₂ and -OH groups. At neutral pH, zeta potential measurements revealed a slightly negative charge (−5.6 ± 4.3 mV), while protonation at lower pH levels enhanced electrostatic interactions with the negatively charged algal biomass. Magnetic separation of the cobalt-adsorbed biomass achieved efficiencies ranging from 94.9% to 99.2% within 60 s, significantly outperforming conventional sedimentation methods. SEM and FTIR analyses confirmed the binding of nanoparticles to algal cell walls. The even distribution of MgFe₂O₄ nanoparticles on algal surfaces was further validated by TEM imaging, and the strong magnetic properties of the nanoparticles enabled rapid and efficient separation under an external magnetic field. Full article

The development of polymer binders with tailored functionalities and green manufacturing processes is highly needed for high-performance lithium–sulfur batteries. In this study, a readily hydrolyzable 3,9-divinyl-2,4,8,10-tetraoxaspiro-[5.5]-undecane is utilized to prepare a water-based binder. Specifically, the acrolein produced by hydrolysis undergoes in situ polymerization to form a linear polymer, while the other hydrolyzed product, pentaerythritol, physically crosslinks these polymer chains via hydrogen bonding, generating a network polymer (BTU). Additionally, gallic acid (GA), a substance derived from waste wood, is further introduced into BTU during slurry preparation, forming a biphenol-containing binder (BG) with a multi-hydrogen-bonded structure. This resilience and robust cathode framework effectively accommodate volumetric changes during cycling while maintaining efficient ion and electron transport pathways. Furthermore, the abundant polar groups in BG enable strong polysulfide adsorption. As a result, sulfur cathode with a high mass loading of 5.3 mg cm⁻² employing the BG (7:3) binder still retains an areal capacity of 4.7 mA h cm⁻² after 50 cycles at 0.1 C. This work presents a sustainable strategy for battery manufacturing by integrating renewable biomass-derived materials and eco-friendly aqueous processing to develop polymer binders, offering a green pathway to high-performance lithium–sulfur batteries. Full article

Exploring advanced sulfur cathode materials is important for the development of lithium-sulfur batteries (LSBs), but they still present challenges. Herein, zinc oxide dots-modified vanadium nitride flower-like heterojunctions (Zn-QDs-VN) as sulfur hosts are prepared by a phase separation strategy. Characterizations confirm that the flower structure with high specific surface area and pores improves active site exposure and electron/mass transfer. In situ phase separation enriches the Zn-QDs-VN interface, addressing the issues of uneven distribution and interface reduction of Zn-QDs-VN. Further theoretical computations reveal that ZnO-QDs-VN with optimized intermediate spin states can constitute a stable LiS* bond sequence, which can conspicuously facilitate the adsorption and conversion of LiPSs and reduce the battery reaction energy barrier. Therefore, the ZnO-QDs-VN@S cathode shows a high initial specific capacity of 1109.6 mAh g⁻¹ at 1.0 C and long cycle stability (maintaining 984.2 mAh g⁻¹ after 500 cycles). Under high S loading (8.5 mg cm⁻²) and lean electrolyte conditions (E/S = 6.5 μL mg⁻¹), it also exhibits a high initial area capacity (10.26 mAh cm⁻²) at 0.2 C. The interfacial synergistic effect accelerates the adsorption and conversion of LiPSs and reduces the energy barriers in cell reactions. The study provides a new method for designing heterojunctions to achieve high-performance LSBs. Full article

In the pursuit of advancing sustainable energy storage solutions, solid-state batteries (SSBs) have emerged as a formidable contender to traditional lithium-ion batteries, distinguished by their superior energy density, augmented safety measures, and improved cyclability. Amid escalating concerns regarding resource scarcity, environmental ramifications, and the safety hazards posed by lithium-ion technologies, the exploration into non-lithium SSBs has emerged as a crucial frontier for technological breakthroughs. This exhaustive review delves into the latest progressions and persisting challenges within the sphere of sodium (Na), potassium (K), and magnesium (Mg) SSBs, spotlighting seminal materials, cutting-edge technologies, and strategic approaches propelling advancements in this vibrant domain. Despite considerable progress, hurdles such as amplifying ionic conductivity, mitigating the intricacies at the electrode–electrolyte interface, and realizing scalable production methodologies continue to loom. Nevertheless, the trajectory for non-lithium SSBs holds considerable promise, poised to redefine the landscape of electric vehicles, portable electronics, and grid stabilization technologies, thereby marking a significant leap toward realizing a sustainable and energy-secure future. This review article aims to provide a detailed overview of the materials and methodologies underpinning the development of these next-generation energy storage devices, underscoring their potential to catalyze a paradigm shift in our approach to energy storage and utilization. Full article