Search Results (100)

The mechanism by which voltage-gated ion channels open and close has been the subject of intensive investigation for decades. For a large class of potassium channels and related sodium channels, the consensus has been that the gating current preceding the main ionic current is a large movement of positively charged segments of protein from voltage-sensing domains that are mechanically connected to the gate through linker sections of the protein, thus opening and closing the gate. We have pointed out that this mechanism is based on evidence that has alternate interpretations in which protons move. Very little literature considers the role of water and protons in gating, although water must be present, and there is evidence that protons can move in related channels. It is known that water has properties in confined spaces and at the surface of proteins different from those in bulk water. In addition, there is the possibility of quantum properties that are associated with mobile protons and the hydrogen bonds that must be present in the pore; these are likely to be of major importance in gating. In this review, we consider the evidence that indicates a central role for water and the mobility of protons, as well as alternate ways to interpret the evidence of the standard model in which a segment of protein moves. We discuss evidence that includes the importance of quantum effects and hydrogen bonding in confined spaces. K⁺ must be partially dehydrated as it passes the gate, and a possible mechanism for this is considered; added protons could prevent this mechanism from operating, thus closing the channel. The implications of certain mutations have been unclear, and we offer consistent interpretations for some that are of particular interest. Evidence for proton transport in response to voltage change includes a similarity in sequence to the H_v1 channel; this appears to be conserved in a number of K⁺ channels. We also consider evidence for a switch in -OH side chain orientation in certain key serines and threonines. Full article

This study focuses on addressing the issues of water flooding and mass transfer limitations in proton exchange membrane fuel cells (PEMFCs) under high current density conditions. A multi-scale gradient pore gas diffusion layer (GDL) is designed to enhance fuel cell performance. The pore structure is precisely controlled using a self-assembled mold, resulting in the fabrication of a GDL with a gradient distribution of pore diameters ranging from 80 to 170 μm. Experimental results indicate that, with the optimized gradient pore GDL, the peak power density of the fuel cell reaches 1.18 W·cm−², representing a 20% improvement compared to the traditional structure. A mechanism analysis reveals that this structure establishes a concentrated water transport pathway through channels while enabling gas diffusion and transport driven by concentration gradients, thereby achieving the collaborative optimization of gas–liquid transport. This approach offers a novel solution for managing water in PEMFCs operating under high current density conditions, and holds significant implications for advancing the commercialization of PEMFC technology. Full article

Proton exchange membrane water electrolyzers (PEMWEs) are a promising technology for green hydrogen production. However, the adoption of PEMWE-based hydrogen production systems remains limited due to several challenges, including high material costs, limited performance and durability, and difficulties in scaling the technology. Computational modeling serves as a powerful tool to address these challenges by optimizing system design, improving material performance, and reducing overall costs, thereby accelerating the commercial rollout of PEMWE technology. Despite this, conventional models often oversimplify key components, such as porous transport and catalyst layers, by assuming constant porosity and neglecting the spatial heterogeneity found in real electrodes. This simplification can significantly impact the accuracy of performance predictions and the overall efficiency of electrolyzers. This study develops a mathematical framework for modeling variable porosity distributions—including constant, linearly graded, and stepwise profiles—and derives analytical expressions for permeability, effective diffusivity, and electrical conductivity. These functions are integrated into a three-dimensional multi-domain COMSOL simulation to assess their impact on electrochemical performance and transport behavior. The results reveal that although porosity variations have minimal effect on polarization at low voltages, they significantly influence internal pressure, species distribution, and gas evacuation at higher loads. A notable finding is that reversing stepwise porosity—placing high porosity near the membrane rather than the channel—can alleviate oxygen accumulation and improve current density. A multi-factor comparison highlights this reversed configuration as the most favorable among the tested strategies. The proposed modeling approach effectively connects porous media theory and system-level electrochemical analysis, offering a flexible platform for the future design of porous electrodes in PEMWE and other energy conversion systems. Full article

This study experimentally investigates various flow field designs for a direct ethanol-based proton exchange membrane (PEM) fuel cell operated at a temperature above the vaporization temperature of water. It expands the designs of flow fields investigated for high-temperature (HT) direct ethanol fuel cells by comparing four designs. It investigates the performance of these designs at various ethanol concentrations and flow rates. A series of polarization, constant current, and impedance spectroscopy experiments were carried out at different combinations of operating conditions. The result shows that all flow fields provide poorer performance at a high ethanol concentration (6 M), regardless of ethanol inlet flow rates. At a low concentration (3 M), the 2-channel spiral flow field exhibits higher cell power output (12–18% higher) with less mass transport loss and charge transfer resistance compared to other flow fields, although it has some voltage instability. As such, it is identified as a promising design, particularly for higher-power applications. The 4-channel serpentine, dual-triangle sandwich, and hybrid flow fields offer similar cell power output (max power: ~23 mW/cm²) and cell potentials. However, the cell potential instability and mass transport losses are higher in the hybrid flow field compared to the other two designs. Thus, it is not as promising a design for ethanol-based HT-PEM fuel cells. Since the dual-triangle has similar performance to the 4-channel serpentine, it could be an alternative to the serpentine for ethanol-based HT-PEM fuel cells. Full article

Proton exchange membrane fuel cells (PEMFCs) offer a promising zero-emission power solution for maritime transportation, yet thermal management remains challenging due to localized overheating and non-uniform temperature distribution. To address the trade-off between pressure drop and thermal performance in marine PEMFC cooling plates, this study developed and systematically evaluated six flow channel configurations through CFD simulations. Parametric analysis coupled with orthogonal experimental design was employed to explore the effects of secondary flow channel number (N), angle (α), width (d), and spacing (L). The results demonstrated that Type B (parallel flow with secondary channels) reduced the pressure drop by 28.2% while achieving the highest cooling efficiency coefficient (2.66 × 10⁴) compared to conventional configuration. Range analysis further ranked parameter sensitivity and identified optimal parameter combinations for distinct optimization objectives: thermal performance (N = 7, α = 30°, d = 0.5 mm, and L = 2.5 mm), pressure drop (N = 8, α = 75°, d = 1.5 mm, and L = 2.5 mm), and cooling efficiency (N = 8, α = 90°, d = 1.5 mm, and L = 2.5 mm). These findings provide practical guidelines for designing cooling plates that address thermal-hydraulic requirements in marine PEMFC systems, advancing their viability for maritime propulsion applications. Full article

Proton exchange membrane fuel cells (PEMFCs), recognized as promising sources of waste heat for space heating, domestic hot water supply, and industrial thermal applications, have garnered substantial interest owing to their environmentally benign operation and high energy conversion efficiency. Since the uniformity of oxygen diffusion toward catalytic layers critically governs electrochemical performance, this study establishes a three-dimensional, non-isothermal computational fluid dynamics (CFD) model to systematically optimize the cathode flow channel width distribution, targeting the maximization of power output through enhanced reactant homogeneity. Numerical results reveal that non-uniform flow channel geometries markedly improve oxygen distribution uniformity, reducing the flow inhomogeneity coefficient by 6.6% while elevating maximum power density and limiting current density by 9.1% and 7.8%, respectively, compared to conventional equal-width designs. There were improvements attributed to the establishment of longitudinal oxygen concentration gradients and we alleviated mass transfer limitations. Synergistic integration with gas diffusion layer (GDL) gradient porosity optimization further amplifies performance, yielding a 12.4% enhancement in maximum power density and a 10.4% increase in limiting current density. These findings validate the algorithm’s efficacy in resolving coupled transport constraints and underscore the necessity of multi-component optimization for advancing PEMFC design. Full article

The performance of electrodes is the most critical factor determining the output characteristics of high-temperature proton exchange membrane fuel cells (HT-PEMFCs), and the electrode structure directly determines the strength of mass transfer and electrochemical reactions. Therefore, exploring the mechanism of increasing the specific surface area of electrodes is crucial for the design of electrode structures. In this paper, the electrochemical characteristics and mass transport of an HT-PEMFC are investigated based on a three-dimensional single-channel model, and a mathematical model of the fin structure on the electrode surface is established to make comparisons with calculations. The results indicate that the oxygen mole concentration decreases with an increase in fin density. Meanwhile, the fuel cell reaches optimal performance at a low operating voltage and in high fin density conditions. In addition, the output performance of the PEMFC increases with the aspect ratio. Finally, the potential distribution of the simulation results coincides with the theoretical model, and the mechanism of electrode polarization on the performance of fin geometry can significantly support the interpretation of kinetic characteristics obtained from simulations. The research result contributes to the efficient design and preparation of future electrode structures of HT-PEMFCs. Full article

With the implementation of strict emission regulations, new energy technologies are widely used in the field of maritime transportation. Fuel cells can be used as the power sources of ships due to the advantages of high efficiency, low noise and zero emissions. In this study, a three-dimensional non-isothermal numerical model of a high temperature proton exchange membrane fuel cell (HT-PEMFC) is established and used to investigate the effect of a flow field with baffles on cell performance. The effects of the number, height and length of baffles in the flow field on the species concentration distribution, current density and power density are comprehensively studied. Compared with the traditional straight channel, the baffles in the channel can effectively improve cell performance. When the number of baffles is nine, the height of the baffles is 0.75 mm and the length of the baffles is 1 mm, the current density is increased from 1.390 A/cm² to 1.524 A/cm² at a voltage of 0.4 V, which is an increase of 9.64%. This study can provide guidelines for flow channel design. Full article

The current opinion manuscript posits that not only Piezo2 voltage block, but also proton affinity and availability in relation to Piezo2, a mechanically gated ion channel, may count in the mediation of pain and its sensitivity. Moreover, this paper argues that autonomously acquired Piezo2 channelopathy on somatosensory terminals is likely the initiating peripheral impaired input source that drives the central sensitization of spinal nociceptive neurons on the chronic path as being the autonomous pain generator. In parallel, impaired proprioception and the resultant progressive deficit in neuromuscular junctions of motoneurons might be initiated on the chronic path by the impairment of the proton-based ultrafast proprioceptive feedback to motoneurons due to disconnection through vesicular glutamate transporter 1. The irreversible form of this autonomously acquired Piezo2 ion channel microdamage, in association with genetic predisposition and/or environmental risk factors, is suggested to lead to progressive motoneuron death in addition to loss of pain sensation in amyotrophic lateral sclerosis. Furthermore, the impairment of the proton-based ultrafast long-range oscillatory synchronization to the hippocampus through vesicular glutamate transporter 2 may gain further importance in pain modulation and formation on the chronic path. Overall, this novel, unaccounted Piezo2-initiated protonic extrafast signaling, including both the protonic ultrafast proprioceptive and the rapid nociceptive ones, within the nervous system seems to be essential in order to maintain life. Hence, its microdamage promotes neurodegeneration and accelerates aging, while the complete loss of it is incompatible with life sustainment, as is proposed in amyotrophic lateral sclerosis. Full article

The present study investigated the ¹H Nuclear Magnetic Resonance (NMR) spectra of hydrogen-rich water (HRW) produced using the EVObooster device. The analyzed HRW has pH = 7.1 ± 0.11, oxidation–reduction potential (ORP) of (−450 ± 11) mV, and a dissolved hydrogen concentration of 1.2 ppm. The control sample was tap water filtered by patented technology. A 600 NMR spectrometer was used to measure NMR spectra. Isotropic 1H nuclear magnetic shielding constants of the most stable clusters (H₂O)_n with n from 3 to 28 have been calculated by employing the gauge-including-atomic-orbital (GIAO) method at the MPW1PW91/6-311+G(2d,p) density function level of theory (DFT). The HRW chemical shift is downfield (higher chemical shifts) due to increased hydrogen bonding. More extensive formations were formed in HRW than in control filtered tap water. The exchange of protons between water molecules is rapid in HRW, and the ¹H NMR spectra are in fast exchange mode. Therefore, we averaged the calculated chemical shifts of the investigated water clusters. As the size of the clusters increases, the number of hydrogen bonds increases, which leads to an increase in the chemical shift. The dependence is an exponential saturation that occurs at about N = 10. The modeled clusters in HRW are structurally stabilized, suggesting well-ordered hydrogen bonds. In the article, different processes are described for the transport of water molecules and clusters. These processes are with aquaporins, fusion pores, gap-junction channels, and WAT FOUR model. The exponential trend of saturation shows the dynamics of water molecules in clusters. In our research, the chemical shift of 4.257 ppm indicates stable water clusters of 4–5 water molecules. The pentagonal rings in dodecahedron cage H₃O⁺(H₂O)₂₀ allow for an optimal arrangement of hydrogen bonds that minimizes the potential energy. Full article

Cation-pumping membrane pyrophosphatases (mPPases; EC 7.1.3.1) vary in their transport specificity from obligatory H⁺ transporters found in all kingdoms of life, to Na⁺/H⁺-co-transporters found in many prokaryotes. The available data suggest a unique “direct-coupling” mechanism of H⁺ transport, in which the transported proton is generated from nucleophilic water molecule. Na⁺ transport is best rationalized by assuming that the water-borne proton propels a prebound Na⁺ ion through the ion conductance channel (“billiard” mechanism). However, the “billiard” mechanism, in its simple form, is not applicable to the mPPases that simultaneously transport Na⁺ and H⁺ without evident competition between the cations (Na⁺,H⁺-PPases). In this study, we used a pyranine-based fluorescent assay to explore the relationship between the cation transport reactions catalyzed by recombinant Bacteroides vulgatus Na⁺,H⁺-PPase in membrane vesicles. Under appropriately chosen conditions, including the addition of an H⁺ ionophore to convert Na⁺ influx into equivalent H⁺ efflux, the pyranine signal measures either H⁺ or Na⁺ translocation. Using a stopped-flow version of this assay, we demonstrate that H⁺ and Na⁺ are transported by Na⁺,H⁺-PPase in a ratio of approximately 1:8, which is independent of Na⁺ concentration. These findings were rationalized using an “extended billiard” model, whose most likely variant predicts the kinetic limitation of Na⁺ delivery to the pump-loading site. Full article

In the small intestine, nutrients from ingested food are absorbed and broken down by enterocytes, which constitute over 95% of the intestinal epithelium. Enterocytes demonstrate diet- and segment-dependent metabolic flexibility, enabling them to take up large amounts of glutamine and glucose to meet their energy needs and transfer these nutrients into the bloodstream. During glycolysis, ATP, lactate, and H⁺ ions are produced within the enterocytes. Based on extensive but incomplete glutamine oxidation large amounts of alanine or lactate are produced. Lactate, in turn, promotes hypoxia-inducible factor-1α (Hif-1α) activation and Hif-1α-dependent transcription of various proton channels and exchangers, which extrude cytoplasmic H⁺-ions into the intestinal lumen. In parallel, the vitamin C-dependent and duodenal cytochrome b-mediated conversion of ferric iron into ferrous iron progresses. Finally, the generated electrochemical gradient is utilized by the divalent metal transporter 1 for H⁺-coupled uptake of non-heme Fe²⁺-ions. Iron efflux from enterocytes, subsequent binding to the plasma protein transferrin, and systemic distribution supply a wide range of cells with iron, including erythroid precursors essential for erythropoiesis. In this review, we discuss the impact of vitamin C on the redox capacity of human erythrocytes and connect enterocyte function with iron metabolism, highlighting its effects on erythropoiesis. Full article

Aluminum (Al) makes up a third of the Earth’s crust and is a widespread toxic contaminant, particularly in acidic soils. It impacts crops at multiple levels, from cellular to whole plant systems. This review delves into Al’s reactivity, including its cellular transport, involvement in oxidative redox reactions, and development of specific metabolites, as well as the influence of genes on the production of membrane channels and transporters, alongside its role in triggering senescence. It discusses the involvement of channel proteins in calcium influx, vacuolar proton pumping, the suppression of mitochondrial respiration, and the initiation of programmed cell death. At the cellular nucleus level, the effects of Al on gene regulation through alterations in nucleic acid modifications, such as methylation and histone acetylation, are examined. In addition, this review outlines the pathways of Al-induced metabolic disruption, specifically citric acid metabolism, the regulation of proton excretion, the induction of specific transcription factors, the modulation of Al-responsive proteins, changes in citrate and nucleotide glucose transporters, and overall metal detoxification pathways in tolerant genotypes. It also considers the expression of phenolic oxidases in response to oxidative stress, their regulatory feedback on mitochondrial cytochrome proteins, and their consequences on root development. Ultimately, this review focuses on the selective metabolic pathways that facilitate Al exclusion and tolerance, emphasizing compartmentalization, antioxidative defense mechanisms, and the control of programmed cell death to manage metal toxicity. Full article

Supercapacitors have long suffered from low energy density. Here, we present a high-energy, high-safety, and temperature-adaptable aqueous proton battery utilizing two-dimensional Ti₃C₂T_x MXenes as anode materials. Additionally, our work aims to provide further insights into the energy storage mechanism of Ti₃C₂T_x in acid electrolytes. Our findings reveal that the ion transport mechanism of Ti₃C₂T_x remains consistent in both H₂SO₄ and H₃PO₄ electrolytes. The mode of charge transfer depends on its terminal groups. Specifically, the hydrogen bonding network formed by water molecules adsorbed by hydroxyl functional groups under van der Waals forces enables charge transfer in the form of naked H⁺ through the Grotthuss mechanism. In contrast, the hydrophobic channel formed by oxygen and halogen terminal groups facilitates rapid charge transfers in the form of hydronium ion via the vehicle mechanism, owing to negligible interfacial effect. Herein, we propose an aqueous proton battery based on porous hydroxy-poor Ti₃C₂T_x MXene anode and pre-protonated Cu^II[Fe^III(CN)₆]_2/3∙4H₂O (H-TBA) cathode in a 9.5 M H₃PO₄ solution. This proton battery operates through hydrated H⁺/H⁺ transfer, leading to good electrochemical performance, as evidenced by 26 Wh kg⁻¹ energy density and 162 kW kg⁻¹ power density at room temperature and an energy density of 17 Wh kg⁻¹ and a power density of 7.4 kW kg⁻¹ even at −60 °C. Full article

pH homeostasis is crucial for spermatogenesis, sperm maturation, sperm physiological function, and fertilization in mammals. HCO₃⁻ and H⁺ are the most significant factors involved in regulating pH homeostasis in the male reproductive system. Multiple pH-regulating transporters and ion channels localize in the testis, epididymis, and spermatozoa, such as HCO₃⁻ transporters (solute carrier family 4 and solute carrier family 26 transporters), carbonic anhydrases, and H⁺-transport channels and enzymes (e.g., Na⁺-H⁺ exchangers, monocarboxylate transporters, H⁺-ATPases, and voltage-gated proton channels). Hormone-mediated signals impose an influence on the production of some HCO₃⁻ or H⁺ transporters, such as NBCe1, SLC4A2, MCT4, etc. Additionally, ion channels including sperm-specific cationic channels for Ca²⁺ (CatSper) and K⁺ (SLO3) are directly or indirectly regulated by pH, exerting specific actions on spermatozoa. The slightly alkaline testicular pH is conducive to spermatogenesis, whereas the epididymis’s low HCO₃⁻ concentration and acidic lumen are favorable for sperm maturation and storage. Spermatozoa pH increases substantially after being fused with seminal fluid to enhance motility. In the female reproductive tract, sperm are subjected to increasing concentrations of HCO₃⁻ in the uterine and fallopian tube, causing a rise in the intracellular pH (pH_i) of spermatozoa, leading to hyperpolarization of sperm plasma membranes, capacitation, hyperactivation, acrosome reaction, and ultimately fertilization. The physiological regulation initiated by SLC26A3, SLC26A8, NHA1, sNHE, and CFTR localized in sperm is proven for certain to be involved in male fertility. This review intends to present the key factors and characteristics of pH_i regulation in the testes, efferent duct, epididymis, seminal fluid, and female reproductive tract, as well as the associated mechanisms during the sperm journey to fertilization, proposing insights into outstanding subjects and future research trends. Full article