Search Results (4,933)

This study develops a multi-stage, Arrhenius-type reaction rate model for exothermic heat release during thermal runaway (TR) that depends on the local active material temperature, T_Cell, and the remaining reactant fraction, Y. Model parameters are identified from an accelerating rate calorimetry (ARC) test on an NMC721 pouch cell. Validation across other cell formats (cylindric and prismatic) and cathode chemistries (LCO, LMO, NCA, LFP) is left for future work. Model performance is evaluated in a 3D CFD (AVL FIRE™ M 2021.2) representation of the ARC assembly and benchmarked against Gaussian and polynomial one-step TR formulations that depend solely on T_Cell. The three TR models are further applied to a generic 4S4P pouch cell module under stagnant and actively cooled conditions to assess thermal propagation. In the ARC test, the Arrhenius-type model shows improved agreement with measured cell skin temperatures for the NMC721 cell; in the 4S4P module, it exhibits a trend toward higher thermal propagation rates relative to the Gaussian and polynomial models. Full article

Plant Microbial Fuel Cells (PMFCs) represent a promising technology that uses electroactive bacteria to convert the chemical energy in organic matter into electrical energy. The addition of carbon pellet on electrodes may increase the specific surface area for colonization via bacteria. Use of nutrients such as urea could enhance plant growth. Our study aims to address the following questions: (1) Does carbon pellet layering affect the electrical performance of PMFCs? (2) Does urea treatment of the plants used to feed the PMFCs affect the electrical performance? A new prototype of PMFC has been tested: the plant pot is on the top, drainage water percolates to the tub below, containing the Microbial Fuel Cells (MFCs). To evaluate the best layering setup, two groups of MFCs were constructed: a “Double layer” group (with carbon pellet both on the cathode and on the anode), and a “Single layer” group (with graphite only on the cathode). All MFCs were plant-fed by Spathiphyllum lanceifolium L leachate. After one year, each of the previous two sets has been divided into two subsets: one wetted with percolate from plants fertilized with urea, and the other with percolate from unfertilized plants. Open circuit voltage (mV), short circuit peak current, and short circuit current after 5 s (mA) produced values that were measured on a weekly basis. PMFCs characterized by a “Single layer” group performed better than the “Double layer” group most times, in terms of higher and steadier values for voltage and calculated power. Undesirable results regarding urea treatment suggest the use of less concentrated urea solution. The treatment may provide consistency but appears to limit voltage and peak values, particularly in the “Double layer” configuration. Full article

Potassium–selenium (K-Se) batteries have emerged as a promising energy storage system in view of their high theoretical energy density and low cost. However, their practical application is restricted due to challenges such as polyselenide shuttling, low redox activity, and significant cathode volume expansion during cycling, leading to inferior Coulombic efficiency and a short cycling lifespan. Carbon-based materials, with their superior electronic conductivity, adjustable pore structures, and robust chemical stability, have been extensively studied and employed as cathode materials in K-Se batteries, demonstrating remarkable potential in addressing the above-mentioned issues. Considering the rapidly growing research interest in this topic in recent years, herein, we comprehensively summarize recent advances in the application of carbon-based materials as cathodes in K-Se batteries. First, we introduce the properties, key challenges, and optimization strategies of K-Se batteries, including encapsulating Se within carbon materials, engineering chemisorptive hosts, and electrocatalyzing redox reactions. Furthermore, we discuss the relationship between fabrication strategies, micro/nanostructures, and electrochemical performances. Finally, we propose future prospects for the rational design and application of carbon-based cathodes in K-Se batteries and other alkaline metal–chalcogen batteries. Full article

Aqueous zinc-ion batteries (ZIBs) have emerged as a promising candidate for large-scale energy storage due to their inherent safety, low cost, and environmental friendliness. However, manganese dioxide (MnO₂)-based cathodes, which are widely studied for ZIBs owing to their high theoretical capacity and low cost, face severe capacity fading issues that hinder the commercialization of ZIBs. This performance degradation mainly stems from the weak van der Waals forces between MnO₂ layers leading to structural collapse during repeated Zn²⁺ insertion and extraction; it is also exacerbated by irreversible Mn dissolution via Mn³⁺ disproportionation that depletes active materials, and further aggravated by dynamic electrolyte pH fluctuations promoting insulating zinc hydroxide sulfate (ZHS) formation to block ion diffusion channels. To address these interconnected challenges, in this study, a synergistic strategy was developed combining crystal engineering and pH buffer regulation. We synthesized three MnO₂ polymorphs (α-, δ-, γ-MnO₂), identified δ-MnO₂ with flower-like microspheres as optimal, and introduced sodium dihydrogen phosphate (NaH₂PO₄) as a pH buffer (stabilizing pH at 2.8 ± 0.2). The modified electrolyte improved δ-MnO₂ wettability (contact angle of 17.8° in NaH₂PO₄-modified electrolyte vs. 26.1° in base electrolyte) and reduced charge transfer resistance (Rct = 78.17 Ω), enabling the optimized cathode to retain 117.25 mAh g⁻¹ (82.16% retention) after 2500 cycles at 1 A g⁻¹. This work provides an effective strategy for stable MnO₂-based ZIBs, promoting their application in renewable energy storage. Full article

This study investigates the impact of vibration frequency on the performance of a 10-cell open-cathode direct methanol fuel cell (OC-DMFC) stack. Experiments were conducted using three different vibration frequencies (15, 30, and 60 Hz) and compared against a baseline condition without vibration. Performance was evaluated under varying methanol–water fuel flow rates (1, 5, 25, and 50 mL·min⁻¹) while maintaining constant operating conditions: methanol temperature at 70 °C, methanol concentration at 1 M, and cathode air flow velocity at 4.8 m·s⁻¹. The optimal performance was observed at a fuel flow rate of 5 mL·min⁻¹, where the maximum power density reached 26.05 mW·cm⁻² under 15 Hz vibration—representing a 14% increase compared to the non-vibrated condition. These findings demonstrate that low-frequency vibration can enhance fuel cell performance by improving mass transport characteristics. Full article

A hydrophobic deep eutectic solvent (HDES) composed of Aliquat 336, decanoic acid, and n-hexanol, diluted with kerosene, was investigated for the selective leaching of LiNi_0.33Mn_0.33Co_0.33O₂ (NMC-111) cathode materials. While conventional choline chloride-based DESs co-dissolve Li and transition metals almost completely, the present HDES–acid hybrid system deliberately sacrifices maximum recovery to achieve selectivity. In combination with a low concentration of H₂SO₄, the HDES enabled preferential dissolution of Co and Ni (~84% and ~80% after 6 h at 90 °C, respectively), while Li and Mn largely remained in the solid residue (>93%). Kinetic modeling indicated that the process is controlled by a surface chemical reaction with apparent activation energies of ~~49 kJ mol⁻¹ (for Ni recovery) and ~51 kJ mol⁻¹ (for Co recovery). The leaching residues were enriched in stable Li-Mn-O phases in a way that offers a basis for stepwise recovery. These findings show that hydrophobic eutectic media coupled with mild acid activation provide a sustainable pathway for the selective recycling of LIB cathodes. Full article

The paper presents experimental results for a modified pulsed plasma thruster (PPT) with solid propellant, using a coaxial anode–cathode design. Graphite from pencil leads served as propellant, and a tungsten trigger electrode was tested to reduce carbonization effects. Experiments were performed in a vacuum chamber at 0.001 Pa, employing diagnostics such as discharge current/voltage recording, power measurement, ballistic pendulum, time-of-flight (TOF) method, and a Faraday cup. Current and voltage waveforms matched an oscillatory RLC circuit with variable plasma channel resistance. Key discharge parameters were measured, including current pulse duration/amplitude and plasma channel formation/decay dynamics. Impulse bit values, obtained with a ballistic pendulum, reached up to 8.5 μN·s. Increasing trigger capacitor capacitance reduced thrust due to unstable “pre-plasma” formation and partial pre-discharge energy loss. Using TOF and Faraday cup diagnostics, plasma front velocity, ion current amplitude, current density, and ion concentration were determined. Tungsten electrodes produced lower charged particle concentrations than graphite but offered better adhesion resistance, minimal carbonization, and stable long-term performance. The findings support optimizing trigger electrode materials and PPT operating modes to extend lifetime and stabilize thrust output. Full article

The development of single-crystal Ni-rich layered cathode materials (SC-NCMs) is regarded as an effective strategy to address the mechanical failure issues commonly associated with polycrystalline counterparts. However, the industrial production of SC-NCM faces challenges such as lengthy processing steps, high manufacturing costs, and inconsistent product quality. In this study, we innovatively propose a metal/organic framework (MOF)-mediated one-step synthesis strategy to achieve controllable structural preparation and in situ Nb⁵⁺ doping in SC-NCM. Using a Ni–Co–Mn-based MOF as both precursor and self-template, we precisely regulated the thermal treatment pathway to guide the nucleation and oriented growth of high-density SC-NCM particles. Simultaneously, Nb⁵⁺ was pre-anchored within the MOF framework, enabling atomic-level homogeneous doping into the transition metal layers during crystal growth. Exceptional electrochemical performance is revealed in the in situ Nb-doped SC-NCM, with an initial discharge capacity reaching 176 mAh/g at a 1C rate and a remarkable capacity retention of 86.36% maintained after 200 cycles. This study paves a versatile and innovative pathway for the design of high-stability, high-energy-density cathode materials via a MOF-mediated synthesis strategy, enabling precise manipulation of both morphology and chemical composition. Full article

With the rapid advancement of energy storage technologies, there is a growing demand for affordable, efficient, and environmentally benign battery systems. Sodium-ion batteries (SIBs) present a promising alternative to lithium-ion systems due to sodium’s high abundance and similar electrochemical properties. Particular attention is given to developing NASICON -sodium (Na) super ionic conductor, type cathode materials, especially Na3V2(PO4)3, which exhibits high thermal and structural stability. This study focuses on the sol–gel synthesis of Na₃V₂(PO₄)₃ using citric acid and ethylene glycol, as well as investigating the effect of annealing temperature (400–1000 °C) on its structural and electrochemical properties. Phase composition, morphology, textural characteristics, and electrochemical performance were systematically analyzed. Above 700 °C, a highly crystalline NASICON phase free of secondary impurities was formed, as confirmed by X-ray diffraction (XRD). Microstructural evolution revealed a transition from a loose amorphous structure to a dense granular morphology, accompanied by changes in specific surface area and porosity. The highest surface area (67.40 m²/g) was achieved at 700 °C, while increasing the temperature to 1000 °C caused pore collapse due to sintering. X-ray photoelectron spectroscopy (XPS) confirmed the predominant presence of V³⁺ ions and the formation of V⁴⁺ at the highest temperature. The optimal balance of high crystallinity, uniform elemental distribution, and stable texture was achieved at 900 °C. Electrochemical testing in a Na/NVP half-cell configuration delivered an initial capacity of 70 mAh/g, which decayed to 55 mAh/g by the 100th cycle, attributed to solid-electrolyte interphase (SEI) formation and irreversible Na⁺ trapping. These results demonstrate that the proposed approach yields high-quality Na₃V₂(PO₄)₃ cathode materials with promising potential for sodium-ion battery applications. Full article

Traditional liquid electrolyte batteries face safety concerns such as leakage and flammability, while further optimization has reached a bottleneck. Solid electrolytes are therefore considered a promising solution. Here, a PEO–LiTFSI–LATP (PELT) composite electrolyte was developed by incorporating nanosized Li_1.3Al_0.3Ti_1.7(PO₄)₃ fillers into a polyethylene oxide matrix, effectively reducing crystallinity, enhancing mechanical robustness, and providing additional Li⁺ transport channels. The PELT electrolyte exhibited an electrochemical stability window of 4.9 V, an ionic conductivity of 1.2 × 10⁻⁴ S·cm⁻¹ at 60 °C, and a Li⁺ transference number (tLi+) of 0.46, supporting stable Li plating/stripping for over 600 h in symmetric batteries. More importantly, to address poor electrode–electrolyte contact in conventional layered cells, we proposed an integrated electrode–electrolyte architecture by in situ coating the PELT precursor directly onto LiFePO₄ cathodes. This design minimized interfacial impedance, improved ion transport, and enhanced electrochemical stability. The integrated PELT/LFP battery retained 74% of its capacity after 200 cycles at 1 A·g⁻¹ and showed superior rate capability compared with sandwich-type batteries. These results highlight that coupling LATP-enhanced polymer electrolytes with an integrated architecture is a promising pathway toward high-safety, high-performance solid-state lithium-ion batteries. Full article

The aim of this work was to investigate the evolutionary mechanisms of an artificial sedimentary agglomerate formed by cathodic polarization in natural seawater during its abandonment to a natural environment. Previous studies indicate that the mineralogical evolution of the material is controlled by kinetic factors and/or the local precipitation of aragonite on the brucite surface. However, the observation of the precipitation of metastable phase precipitation during the initial immersion of this material (in powder form) has suggested the possibility of a more complex mechanism. The present study builds upon previous experimental work and includes thermogravimetric analysis and infrared spectrometry. The results are analyzed using numerical experimentation to evaluate the proposed hypotheses. Findings show that the transformation mechanism is characterized by the precipitation of metastable calcium carbonate phases. Under supersaturation conditions, these hydrated phases form on the brucite surface, limiting the mineral’s contact with the solution. The subsequent transformation of these amorphous phases into aragonite further reduces brucite–solution interaction, which explains the persistence of brucite both in the residual powder after 120 h of immersion and in the consolidated material after more than 20 years of exposure to natural seawater. Full article

Microbial electrolysis cells (MECs) present a viable platform for sustainable hydrogen generation from organic waste, but their scalability is limited by cathode performance, cost, and durability. This study evaluates three hybrid carbon nanotube (CNT) cathodes—acid-washed CNT (AW-CNT), thin layer non-acid-washed CNT (TN-NAW-CNT), and thick layer non-acid-washed CNT (TK-NAW-CNT)—each composed of stainless-steel-supported CNTs coated with molybdenum phosphide (MoP). These were benchmarked against woven carbon cloth (WCC) under varied operational conditions. A custom multi-channel reactor operated for 341 days, testing cathode performance across applied voltages (0.7–1.2 V), buffer types (phosphate vs. bicarbonate), pH (7.0 and 8.5), buffer concentrations (10–200 mM), and substrates including acetate, lactate, and treated acid whey. CNT-based cathodes consistently showed higher current densities than WCC across most conditions with significant difference found at higher applied voltages. TK-NAW-CNT achieved peak current densities of 259 A m⁻² at 1.2 V and maintained >41 A m⁻² in real-waste conditions with no added buffer. Long-term performance losses were minimal: 4.5% (TN-NAW-CNT), 0.1% (TK-NAW-CNT), 10.8% (AW-CNT), and 6.8% (WCC). CNT cathodes showed improved performance from reduced resistance and greater electrochemical stability, while proton transfer improvements benefited all materials due to buffer type and pH conditions. These results highlight CNT-based cathodes as promising, scalable alternatives to WCC for energy-positive wastewater treatment. Full article

Major depressive disorder (MDD) is a prevalent and disabling condition. Transcranial direct current stimulation (tDCS) may improve symptoms by modulating neuroplastic and inflammatory mechanisms. This randomized, double-blind, placebo-controlled trial will recruit adult outpatients with MDD showing residual symptoms despite at least four weeks of stable SSRI treatment. Participants will be randomized to active or sham add-on tDCS while continuing their antidepressant regimen. The intervention will consist of 15 sessions over 3 weeks, targeting the left dorsolateral prefrontal cortex (anode F3, cathode F4) at 2 mA for 30 min per session. The primary outcome is the reduction of depressive symptoms measured by the Hamilton Depression Rating Scale-17 (HDRS), with remission defined as HDRS-17 ≤ 7. Secondary outcomes include cognitive performance (attention, executive functioning, memory), serum biomarkers (BDNF, VEGF, NGF, NRG1, angiogenin, IGF1, IL-6, TNF-α), cortical excitability assessed by transcranial magnetic stimulation (motor threshold, silent period, intracortical inhibition/facilitation), and cerebral hemodynamics by transcranial Doppler sonography (blood flow velocity, pulsatility, resistivity). Assessments will occur at baseline, post-treatment, and 3- and 6-month follow-ups. This trial aims to evaluate the efficacy of adjunctive tDCS in MDD with residual symptoms and its biological correlates, bridging clinical improvement with electrophysiological and neurovascular mechanisms. Full article

MXenes, a rapidly emerging family of two-dimensional transition metal carbides and nitrides, have attracted considerable attention in recent years for their potential in next-generation energy storage technologies. In solid-state batteries (SSBs), they combine metallic-level conductivity (>10³ S cm⁻¹), adjustable surface terminations, and mechanical resilience, which makes them suitable for diverse functions within the cell architecture. Current studies have shown that MXene-based anodes can deliver reversible lithium storage with Coulombic efficiencies approaching ~98% over 500 cycles, while their use as conductive additives in cathodes significantly improves electron transport and rate capability. As interfacial layers or structural scaffolds, MXenes effectively buffer volume fluctuations and suppress lithium dendrite growth, contributing to extended cycle life. In solid polymer and composite electrolytes, MXene fillers have been reported to increase Li⁺ conductivity to the 10⁻³–10⁻² S cm⁻¹ range and enhance Li⁺ transference numbers (up to ~0.76), thereby improving both ionic transport and mechanical stability. Beyond established Ti-based systems, double transition metal MXenes (e.g., Mo₂TiC₂, Mo₂Ti₂C₃) and hybrid heterostructures offer expanded opportunities for tailoring interfacial chemistry and optimizing energy density. Despite these advances, large-scale deployment remains constrained by high synthesis costs (often exceeding USD 200–400 kg⁻¹ for Ti₃C₂T_x at lab scale), restacking effects, and stability concerns, highlighting the need for greener etching processes, robust quality control, and integration with existing gigafactory production lines. Addressing these challenges will be crucial for enabling MXene-based SSBs to transition from laboratory prototypes to commercially viable, safe, and high-performance energy storage systems. Beyond summarizing performance, this review elucidates the mechanistic roles of MXenes in SSBs—linking lithiophilicity, field homogenization, and interphase formation to dendrite suppression at Li|SSE interfaces, and termination-assisted salt dissociation, segmental-motion facilitation, and MWS polarization to enhanced electrolyte conductivity—thereby providing a clear design rationale for practical implementation. Full article

With their considerable capacity and structurally favorable characteristics, layered transition metal oxides have become strong contenders for cathode use in sodium-ion batteries (SIBs). Nevertheless, their practical deployment is challenged by pronounced capacity loss, predominantly induced by unstable cathode–electrolyte interphase (CEI) at elevated voltages. In this study, difluoroethylene carbonate (DFEC) is introduced as a functional electrolyte additive to engineer a robust and uniform CEI. The fluorine-enriched CEI effectively suppresses parasitic reactions, mitigates continuous electrolyte decomposition, and facilitates stable Na⁺ transport. Consequently, Na/NaNi_1/3Fe_1/3Mn_1/3O₂ (Na/NFM) cells with 2 wt.% DFEC retain 78.36% of their initial capacity after 200 cycles at 1 C and 4.2 V, demonstrating excellent long-term stability. Density functional theory (DFT) calculations confirm the higher oxidative stability of DFEC compared to conventional solvents, further supporting its interfacial protection role. This work offers valuable insights into electrolyte additive design for high-voltage SIBs and provides a practical route to significantly improve long-term electrochemical performance. Full article