Search Results (1,214)

Aqueous zinc-ion batteries offer a safe and economical platform for large-scale energy storage, yet vanadium oxide cathodes remain hindered by sluggish Zn²⁺ migration, poor electronic conductivity, and structural degradation during cycling. Herein, a PEDOT regulated interfacial engineering strategy is proposed to construct surface modified sodium vanadium oxide nanostructures with coordinated ion and electron transport. The 1P-NaVO cathode retains the layered framework while introducing a PEDOT-derived surface component that strengthens interfacial charge transfer and preserves accessible Zn²⁺ diffusion pathways, delivering 655 mAh g⁻¹ at 0.1 A g⁻¹. Kinetic analyses further reveal accelerated charge storage behavior, including an increased pseudocapacitive contribution, a low charge transfer activation energy of 20.6 kJ mol⁻¹, and improved Zn²⁺ diffusion, with D_Zn²⁺ values of approximately 10^−10.8 to 10^−9.8 cm² s⁻¹. Ex situ XRD and SEM disclose a reversible structural response during Zn²⁺ insertion and extraction, involving interlayer perturbation, local framework relaxation, transient electrolyte-derived surface species, and partial morphology recovery after recharge. These findings show that controlled PEDOT-derived surface regulation promotes efficient coupling between interfacial electron transfer and Zn²⁺ diffusion, offering a practical design principle for durable vanadium-based cathodes in aqueous zinc-ion batteries. Full article

Polymer electrolyte membranes serving in proton exchange membrane fuel cells (PEMFCs) and direct methanol fuel cells (DMFCs) must possess sufficient mechanical–dimensional stability and excellent proton conducting capacity. Derived from the successful syntheses of two different sulfonated poly(aryl ether ketone)s bearing functional amine groups, two series of novel epoxy-crosslinked and silane-crosslinked sulfonated poly(aryl ether ketone) electrolyte networks are constructed for highly conductive and mechanically stable proton exchange membranes. The designed multi-component architecture, which integrates a moderate-ion-exchange-capacity sulfonated poly(aryl ether ketone) (moderate-IEC SPAEK), a high-IEC SPAEK, and a tailored crosslinker (epoxy or silane), enables a breakthrough in decoupling the traditional trade-off between conductivity and stability. The resulting membranes exhibit an outstanding combination of properties: exceptional proton conductivity exceeding 0.18 S cm⁻¹ at 100 °C, tensile strength above 28.80 MPa, and enhanced chemical resistance, thermo-oxidative stability, and competitive direct methanol fuel cell performance. This work establishes a rational design strategy for crosslinked multi-component membranes as a promising platform for next-generation high-performance fuel cells. Full article

The increasing global demand for high-performance, reliable, and sustainable energy storage systems has accelerated the development of supercapacitors as technologies capable of bridging the performance gap between conventional capacitors and batteries. Supercapacitors combine rapid charge–discharge capability, high power density, and exceptional cycle life through charge storage mechanisms based on ion adsorption and fast surface redox reactions at the electrode–electrolyte interface. This review examines the fundamental operating principles, charge storage mechanisms, electrode materials, mechanical and functional properties, fabrication methods, and engineering applications of modern supercapacitors. Carbon-based materials, metal oxides, conducting polymers, MXenes, sulfides, nitrides, borides, and emerging hybrid systems are critically compared in terms of capacitance, energy density, cycling stability, and mechanical robustness. Additionally, recent advances in scalable manufacturing approaches, including thin-film deposition and printing technologies, are discussed alongside key challenges such as limited energy density, interfacial instability, mechanical degradation, electrolyte compatibility, and large-scale processing. By consolidating recent developments across materials science, electrochemistry, and device engineering, this review provides insight into future directions for next-generation high-performance supercapacitor technologies. Full article

Zinc oxide (ZnO) varistors are a core component of surge arresters; their failure can directly affect the secure and reliable operation of power equipment. Therefore, this paper conducts an impulse degradation test on ZnO varistors, combining electrical and microstructural tests to systematically explore the intrinsic correlation mechanism between the electrical properties and microstructural characteristics. Test results show that this type of ZnO varistor is susceptible to side-glaze surface flashover under an impulse current with a waveform of 8/20 μs and an amplitude of 27 kA, and the discharge branches exhibit an extension from the negative electrode towards the positive electrode. Moreover, surface flashover causes the formation of local conductive channels in the side glaze layer, resulting in a significant drop in the direct-current (DC) reference voltage U_1mA. However, the residual voltage U_10kA increases slightly with an increase in the number of impulse groups, with a change in amplitude of less than 1.5%. Additionally, the microstructural testing reveals that the impulse currents cause the bismuth (Bi) element in ZnO grains to precipitate and form more Bi-rich phases at the grain boundaries. This results in an increase in the thickness of the grain boundary layer, which is negatively correlated with the U_1mA. Meanwhile, the grain morphology and size distribution of brand-new samples, samples with different degrees of degradation, and samples with side-glaze surface flashover damage are not significantly different. This is consistent with the fact that the change range of the residual voltage U_10kA during impulse degradation is very small. This test phenomenon indicates that the failure of this type of ZnO varistor to withstand an impulse current with a waveform of 8/20 μs and an amplitude of 27 kA is mainly due to changes in the volt-ampere properties of the small-current regions caused by ion migration within the grain boundary layer. This research provides an experimental basis and theoretical support for improving the impulse withstand capacity of ZnO varistors in their design. Full article

Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) dysfunction is increasingly recognized as a key contributor to a broad spectrum of human diseases beyond classical cystic fibrosis (CF). CFTR is a cAMP-regulated chloride and bicarbonate ion channel expressed in both epithelial and non-epithelial tissues, where it regulates ion homeostasis, mucosal hydration, and cellular signaling. Both inherited CFTR mutations and acquired dysfunction resulting from environmental or inflammatory factors can disrupt these physiological processes and drive disease progression. Current evidence linking CFTR dysregulation to respiratory diseases, such as cystic fibrosis, chronic obstructive pulmonary disease (COPD), asthma, and HIV-associated airway disease, as well as cardiovascular, renal, neurological diseases, and cancer, is comprehensively discussed. Mechanistically, impaired CFTR function promotes oxidative stress, chronic inflammation, epithelial barrier dysfunction, altered mucociliary clearance, and dysregulation of signaling pathways, including NF-κB, TGF-β, PI3K/Akt, MAPK, and Wnt/β-catenin. In the context of HIV infection and cigarette smoke exposure, CFTR suppression is mediated in part by TGF-β signaling and miRNA-dependent mechanisms, resulting in compromised airway defense and increased susceptibility to pulmonary complications. Recent studies further demonstrate that CFTR dysregulation alters the expression of genes involved in fibrosis, inflammation, angiogenesis, and epithelial–mesenchymal transition (EMT). Notably, CFTR may act as either a tumor suppressor or a context-dependent oncogene, depending on tissue type and signaling milieu, highlighting its complex role in cancer biology. Advances in CFTR-targeted therapies, including potentiators, correctors, gene therapy, and combination approaches, have markedly improved outcomes in CF and may offer therapeutic potential for diseases associated with acquired CFTR dysfunction. We summarize the systemic consequences of CFTR dysregulation and the need for further mechanistic and translational research to clarify its role across diverse human diseases. Full article

Green synthesis of silver nanoparticles (CP-AgNPs) using Calotropis procera (CP) offers a sustainable approach to producing multifunctional therapeutic nanomaterials. This study aimed to synthesize CP-AgNPs and evaluate their antimicrobial, antioxidant, anti-inflammatory, and anticancer potential, with a focus on Helicobacter pylori and gastric cancer cells. CP-AgNPs were prepared by phytochemical reduction using CP leaf extract and characterized by UV–Vis, XRD, FTIR, SEM, EDX, TEM, and Zeta. Antibacterial activity against H. pylori, time-kill kinetics, and SEM imaging of membrane damage were performed. Antioxidant (DPPH, ABTS) and anti-inflammatory assays, together with cytotoxicity studies in AGS cells (DAPI, AO/EtBr, and SEM), were also conducted. CP-AgNPs exhibited an SPR peak at 432 nm, face-centered cubic crystallinity, and spherical morphology (8–32 nm). They showed strong, dose-dependent antibacterial activity against H. pylori, surpassing metronidazole at higher doses. Time-kill assays and SEM confirmed membrane disruption. Antioxidant activity was notable (IC₅₀: 40 µg/mL for DPPH; 60 µg/mL for ABTS). CP-AgNPs demonstrated significant anti-inflammatory effects and dose-dependent cytotoxicity in AGS cells, inducing apoptosis and morphological alterations. The broad biological activity of CP-AgNPs likely arises from the synergy between silver ions and CP phytochemicals. Their superior antibacterial effects, combined with antioxidant and anti-inflammatory properties, indicate strong therapeutic potential for gastric diseases. Anticancer activity in AGS cells suggests additional biomedical relevance, which may involve ROS-associated and apoptosis-related pathways, as suggested by previous studies. CP-AgNPs represent a promising natural nanoplatform for managing H. pylori infection, oxidative stress, inflammation, and gastric cancer, warranting further mechanistic and in vivo studies. Full article

Background: Sensorineural hearing loss (SNHL) is increasingly recognized as a disorder involving not only hair-cell damage but also selective degeneration of spiral ganglion neurons (SGNs). Recent single-cell, molecular, and functional studies have refined the classical type I/type II classification of SGNs by identifying distinct Ia, Ib, and Ic subtypes within type I neurons. This review aims to synthesize current evidence on how SGN vulnerability is shaped by the interaction between subtype identity, life stage, and injury context. Methods: We conducted a critical narrative review of recent studies on SGN heterogeneity and subtype-specific vulnerability across development, maturity, and aging, with particular attention to molecular profiling, functional studies, and emerging therapeutic strategies. Results: SGN degeneration in SNHL is not uniform. During development, the available evidence mainly supports the vulnerability of subtype specification, synaptogenesis, and activity-dependent maturation, rather than direct selective degeneration of mature Ia/Ib/Ic identities. In the mature cochlea, subtype-specific differences in synaptic architecture, ion-channel composition, and metabolic demand appear to shape responses to noise, ototoxic drugs, and ischemic stress, with Ic-related populations often showing greater vulnerability. During aging, cumulative mitochondrial dysfunction, oxidative stress, chronic inflammation, and declining neurotrophic support may progressively unmask differences in subtype resilience and contribute to age-related auditory decline. Conclusions: A lifespan-oriented and subtype-informed framework may improve the current understanding of selective SGN degeneration and support the development of more precise neuroprotective and reparative strategies for SNHL. Full article

The rapid expansion of artificial intelligence has intensified the demand for hardware systems capable of emulating brain-like information processing with high accuracy, energy efficiency, and reliability. Neuromorphic computing based on memristive artificial synapses has emerged as a promising approach to overcome the limitations of conventional von Neumann architectures. Although inorganic and oxide-based synaptic memristors have been widely explored for neuromorphic systems, they often suffer from poor linearity, asymmetric potentiation/depression behavior, limited conductance states, and device variability, which restrict learning accuracy and scalability. In contrast, polymer-based memristors have gained significant attention owing to their intrinsic advantages, including mechanical flexibility, molecular tunability, controllable electronic/ionic transport, low-temperature processability, and compatibility with large-area fabrication. This review critically examines recent advances in polymer—based memristive materials and devices for achieving linear and symmetric artificial synaptic behavior. Polymer synapses are classified into pure polymer, polymer composite, and polymer-hybrid systems through a mechanism to function framework. Rather than providing a general compilation of organic memristor studies, this review analyzes how polymer chemistry, ion-migration control, trap state distribution, redox activity, electrode selection, active layer thickness, and interface engineering govern conductance update linearity, symmetry, and uniformity. Fundamental switching mechanisms, material classifications, device architectures, key synaptic characteristics, and system-level neuromorphic performance, including pattern-recognition applications, are critically discussed. By explicitly linking material and device design to conductance update fidelity, learning accuracy, training convergence, and pattern-recognition reliability, this review provides practical design guidelines and future perspectives for next-generation polymer-based neuromorphic hardware with improved linearity, symmetry, reliability, and scalability. Full article

Sodium-ion batteries (SIBs) are emerging as a viable alternative to lithium-ion batteries (LIBs) due to their material sustainability and cost-effectiveness, helping address the high costs, supply limits, and environmental concerns associated with lithium. This paper reviews SIB materials, designs, and applications, and surveys their electrochemical performance, challenges, and future prospects. Recent advances in electrode materials (e.g., layered oxides, hard carbon composites, metallic alloys) are greatly improving SIB stability, conductivity, capacity, and cycle life. Improvements in both solid-state and liquid electrolytes have likewise enhanced ionic conductivity, capacity retention, thermal stability, and safety. Despite their lower energy density, SIBs tolerate wider temperature ranges and carry a significantly lower risk of thermal runaway compared to lithium-based systems, making them attractive for industrial, transportation, and large-scale power storage. Continuous progress in materials and cell engineering is narrowing the performance gap between SIBs and LIBs. Meanwhile, nascent battery recycling strategies for SIBs show promise for economic and environmental viability. Overall, SIBs represent a promising option for safer, more accessible, and more sustainable energy storage technology. Full article

NASICON-type Na₃V₂(PO₄)₃ (NVP) is widely regarded as a promising cathode for sodium-ion batteries owing to its robust three-dimensional framework and high operating voltage (~3.4 V vs. Na⁺/Na). However, NVP suffers severe capacity degradation under fast-charging conditions due to its intrinsically low electronic conductivity, which critically impedes its practical deployment. Herein, we systematically investigate the fast-charging failure mechanism of NVP and propose a trace Sm³⁺ doping strategy (x = 0.03) to address this limitation. Undoped NVP retains only 13.5% and 56.62% of its initial capacity after 1000 cycles at 5000 mA g⁻¹ and 1307 cycles at 2000 mA g⁻¹, respectively. Post-cycling scanning electron microscopy (SEM) reveals extensive crack formation and particle pulverization, providing direct morphological evidence for structural failure. To overcome this, Sm³⁺-doped Na₃V_1.97Sm_0.03(PO₄)₃/C (NVPSM) is synthesized via a sol–gel method. X-ray diffraction (XRD) confirms that the NASICON phase is preserved. Raman spectroscopy reveals an improved graphitization degree (I_D/I_G = 0.97 vs. 1.02 for NVP), and X-ray photoelectron spectroscopy (XPS) verifies the V³⁺ oxidation state and the incorporation of Sm³⁺. Electrochemically, NVPSM achieves capacity retentions of 60.3% after 2300 cycles at 5000 mA g⁻¹ and 83.89% after 1436 cycles at 2000 mA g⁻¹. Electrochemical impedance spectroscopy confirms reduced charge-transfer resistance, and post-cycling SEM shows markedly improved structural integrity. These results demonstrate that trace rare-earth doping effectively mitigates fast-charging-induced structural failure in NVP-based cathodes. Full article

Since the first successful synthesis of borophene in 2015, this atomically thin boron allotrope has attracted extensive attention due to its polymorphic structures, metallic conductivity, and outstanding mechanical flexibility. As a new member of the two-dimensional (2D) materials family, borophene exhibits a unique triangular lattice with tunable hexagonal vacancies, leading to rich structural diversity and anisotropic physical properties. Recent breakthroughs in synthesis—particularly molecular beam epitaxy (MBE), chemical vapor deposition (CVD), and solvothermal-assisted liquid-phase exfoliation (S-LPE)—have significantly expanded the accessible structural phases and improved control over film quality and stability. Meanwhile, borophene’s distinctive combination of structural and electronic characteristics has enabled its rapid development in both energy and biomedical applications. In energy storage, borophene serves as a promising anode material for lithium/sodium-ion batteries and a lightweight medium for hydrogen storage and supercapacitors, owing to its metallic conductivity, high surface charge density, and large adsorption capacity. In biomedicine, borophene-based nanoplatforms exhibit excellent photothermal conversion efficiency, enabling multifunctional roles in cancer diagnosis and therapy. Despite these advances, several challenges—such as environmental instability, oxidation susceptibility, and limited scalable synthesis—continue to restrict practical implementation. Future progress will depend on chemical functionalization, surface passivation, and machine-learning-assisted materials design to achieve oxidation-resistant, large-area, and biocompatible borophene derivatives. This review summarizes recent advances in borophene synthesis, structural engineering, and multifunctional applications, while outlining key scientific challenges and future opportunities for the realization of borophene-based materials in next-generation energy and biomedical systems. Full article

This study presents a hierarchical conductive-network strategy to overcome the performance trade-off in cement structural supercapacitors (CSSCs). By incorporating one-dimensional carbon nanotubes (CNTs) and two-dimensional graphene oxide (GO) into Portland cement, we simultaneously enhance its electrochemical and mechanical properties. The approach exploits the complementary roles of the two nanomaterials: CNTs establish a three-dimensional percolation network that facilitates electron transport, while GO promotes formation of a denser calcium silicate hydrate (C-S-H) gel and refines the pore structure by complexing with calcium ions, thereby improving ionic pathways. The k12gc sample attains a specific capacitance of 66.8 F g⁻¹ at 0.1 mA cm⁻², a 58.4% rise in conductivity and a 63% reduction in charge-transfer resistance. At the same time, the composite reduces harmful macropores by 27.9% and strengthens the material, with compressive and flexural strengths increasing by 4.8% and 8.3%, respectively. This work establishes a rational design principle based on functional division between CNTs and GO for developing high-performance, multifunctional CSSCs. Full article

Pharmacotherapy of neuropathic pain (NP) remains challenging due to its heterogeneous etiology, lack of objective diagnostic tools, and the limited efficacy of currently available treatments, including antidepressants, anticonvulsants, and local anesthetics. Therefore, the search for novel therapies with improved analgesic efficacy and reduced adverse effects is of growing importance. In this context, natural alkaloids have emerged as promising candidates, demonstrating analgesic potential in both diabetes-induced neuropathy and various experimental models of NP. This review outlines NP pathophysiology, emphasizing maladaptive changes within the somatosensory nervous system, including peripheral and central sensitization, as well as glial cell activation. Furthermore, it discusses the mechanisms through which alkaloids may modulate NP-related pathways, with particular focus on their interactions with ion channels, signaling pathways, inflammatory responses, and oxidative stress. A literature search was conducted using the Scopus, Google Scholar and PubMed databases for papers published between 2015 and 2026, using the keywords “alkaloids” and “neuropathic pain”, and focused on recent findings regarding the antinociceptive effects of berbamine, tetrandrine, fangchinoline, and sinomenine, and their derivatives. The analysis indicates that, despite promising preclinical evidence, further rigorous preclinical and clinical studies are necessary to fully assess their therapeutic potential in the treatment of NP. Full article

The growing penetration of renewable energy sources has intensified the demand for safe, sustainable, and cost-effective energy-storage technologies. Aqueous lithium-ion batteries are promising candidates because of their intrinsic safety and high ionic conductivity, though their deployment is limited by narrow electrochemical stability window of water. Lithium titanate oxide (LTO) has emerged as an ideal anode material for aqueous systems because of its exceptional structural stability, negligible volume change during lithiation/delithiation, and relatively high operating potential that suppresses hydrogen evolution. This review examines the peer-reviewed literature (2010–2026) on LTO-based aqueous lithium-ion batteries, focusing on the interdependence between material synthesis, electrode fabrication, electrolyte engineering, and electrochemical performance. Scalable fabrication techniques, such as spray deposition and tape casting, are discussed alongside their pact on electrode quality. Attention is given to water-in-salt, gel-polymer, and localized high-concentration electrolytes that expand the stability window and improve interfacial behavior. Overall, the review highlights how electrolyte design, electrode architecture, and processing methods can be jointly tailored to support stable and scalable LTO-based aqueous lithium-ion batteries systems. Full article

Candida albicans is a common opportunistic pathogen. Long-term use of azole antifungals faces challenges like resistance, necessitating novel agents. Tea tree oil (TTO), a natural broad-spectrum antimicrobial, shows promise, but its molecular mechanisms, particularly concerning novel cell death pathways, require clarification. This study comprehensively evaluated the antifungal mechanism of TTO against C. albicans using transcriptomics. Antifungal susceptibility assays were conducted to assess the effects of TTO and its components (4-terpineol, terpenes, and γ-pinene) on the growth of C. albicans hyphae and biofilms. Fluorescent labeling and biochemical analysis were employed to detect ferroptosis markers. Transcriptomic results indicate that TTO induces 423 differentially expressed genes and systematically inhibits the development of C. albicans hyphae through mechanisms such as oxidative stress, iron homeostasis disruption, disruption of cell wall integrity, and interference with ergosterol metabolism. Notably, the significant enrichment of redox enzyme activity and iron ion binding functions, along with changes in the glutathione metabolic pathway, suggest that ferroptosis may be involved in this process. Subsequent studies revealed that the compound 4-pinene most effectively inhibits the pathogenicity of C. albicans by suppressing its adhesion, hyphae formation, and biofilm formation, whereas terpinene induces the accumulation of reactive oxygen species (ROS) and increases lipid peroxidation in C. albicans; furthermore, following treatment with an iron-mediated apoptosis inhibitor, terpinene enhances the viability of the treated C. albicans cells. Full article