Search Results (54)

Photoelectrochemical water splitting (PEC-WS) provides a sustainable route to transform solar energy into hydrogen; however, its overall efficiency is constrained by the inherently slow kinetics of the oxygen evolution reaction. Bismuth vanadate (BiVO₄) is considered an attractive visible-light-responsive photoanode due to its suitable band gap (~2.4 eV) and chemical stability; however, its efficiency is restricted by limited charge transport and significant charge carrier recombination. To overcome these limitations, BiVO₄–MoS₂ (BVO–MS) heterostructures were synthesized through a simple in situ hydrothermal approach, ensuring robust interfacial coupling and uniform dispersion of MS nanosheets over BVO dendritic surfaces. This intimate contact promotes rapid charge transfer and improved light-harvesting capability. Structural and spectroscopic analyses confirmed the formation of monoclinic BVO with uniformly integrated amorphous MS. The optimized BVO–MS10 electrode delivered a photocurrent density of 4.72 mA cm⁻² at 0.6 V vs. SCE, approximately 5.3 times higher than pristine BVO, and achieved an applied bias photon-to-current efficiency of 0.49%. Mott–Schottky analysis revealed a distinct negative shift in the flat-band potential for BVO–MS10, indicative of an upward movement of its conduction band and the establishment of a strong internal electric field that enhances charge separation and interfacial electron transport. These synergistic effects collectively endow the in situ engineered BVO–MS heterostructure with superior PEC water oxidation performance and highlight its promise for efficient solar-driven hydrogen generation. Full article

The commercialization of rechargeable alkaline zinc–air batteries has been constrained by critical challenges associated with the zinc electrode, including passivation, dendrite growth, and hydrogen evolution reaction. These issues severely limit the cycle life and pose a major barrier to large-scale industrial deployment. Integration of porous anode structures and electrode additives—two widely investigated approaches for mitigating challenges related to zinc anode—shows significant promise. However, effectively combining these approaches remains challenging. This study introduces a method for fabricating zinc anodes that can combine the benefits of a porous structure and electrode additive. The polytetrafluoroethylene (PTFE) polymer binder used in fabricating the anode material resulted in a stable scaffold, providing the desired anode porosity of approximately 60% and effectively anchoring ZnO nanoparticles. The zinc anodes prepared using a nickel mesh current collector without any electrode additives demonstrated stable cycling performance, sustaining 350 cycles at a current density of 60 mA g_Zn⁻¹ with a coulombic efficiency of approximately 95%. Incorporating 2 wt.% Bi₂O₃ as an electrode additive further enhanced the cycling performance, achieving 200 stable cycles with 100% coulombic efficiency under an increased current density of 120 mA g_Zn⁻¹, signifying the effectiveness of the proposed fabrication strategy. Full article

Bisphenol A diglycidyl ether (BADGE) is the main component of epoxy resin and is used for the inner coating of canned foods and plastic food containers. BADGE can easily migrate from containers and result in food contamination; the compound is known as an endocrine-disrupting chemical. We previously reported that maternal exposure to bisphenol A bis (2,3-dihydroxypropyl) ether (BADGE·2H₂O), which is the most detected BADGE derivative not only in canned foods but also in human specimens, during gestation and lactation, could accelerate neuronal differentiation in the cortex of fetuses and induce anxiety-like behavior in juvenile mice. In this study, we investigated the effects of low-dose BADGE·2H₂O (1–100 pM) treatment on neurites and the mechanism of neurite outgrowth in cortical neurons. BADGE·2H₂O exposure significantly increased the number of dendrites and neurite length in cortical neurons; these accelerating effects were inhibited by estrogen receptor (ER) antagonist ICI 182,780 and G-protein-coupled estrogen receptor (GPER) antagonist G15. BADGE·2H₂O down-regulated Hes1 expression, which is a transcriptional repressor, and increased levels of neuritogenic factor neurogenin-3 (Ngn3) in the cortical neurons; the changes were significantly blocked by G15. These data suggest that direct BADGE·2H₂O exposure can accelerate neuritogenesis and outgrowth in cortical neurons through down-regulation of Hes1 and by increasing Ngn3 levels through ERs, particularly GPER. Full article

The persistent emphasis on safety issues in lithium-ion batteries (LIBs) with organic liquid electrolytes revolves around thermal runaway and dendrite formation. The high thermal stability and non-leakage properties of polymer electrolytes (PEs) make them attractive as next-generation electrolytes for LIBs. This study presents a blended terpolymer electrolyte (BTPE) membrane, integrating the high ionic conductivity of dual ion conducting polymer electrolytes (DICPEs) with the elevated lithium transference number ($t_{+}$) of single-ion conducting polymer electrolytes (SICPEs). The BTPE was synthesized by blending PAA–PVA with lithiated acrylic acid (LiAA), lithiated 2–acrylamido–2–methylpropane sulfonic acid (LiAMPS), and a 2–hydroxyethyl methacrylate (HEMA)–based terpolymer, using lithium bis(fluorosulfonyl)imide (LiFSI) as the lithium salt. The synthesized BTPE showed excellent physical and electrochemical stability; it also exhibited an enhanced lithium transference number ($t_{+}$ = 0.47) and high ionic conductivity (5.21 × 10⁻⁴ S cm⁻¹ at 30 °C), attributed to the interaction between the FSI anion and the NH group of AMPS. This research presents an innovative strategy for the design of next-generation LIB electrolytes by integrating polymer electrolytes. Full article

The electrochemical CO₂ reduction reaction (CO₂RR) to formate offers a promising pathway to mitigate the energy crisis and realize carbon neutrality. Bismuth (Bi), as a metal catalyst for the CO₂RR, is considered to have great potential in producing formate, yet hindered in low current density and selectivity. Herein, we constructed an oxide-derived copper foam substrate (OD-Cu) to improve the electrocatalytic properties of Bi dendrites loaded on its surface. Bi electrodeposited on the OD-Cu (Bi/OD-Cu) grows as pinecone-like dendrites, exhibiting a high formate faradaic efficiency (FE_formate) of 97.2% and a formate partial current density of ~24 mA·cm⁻² at −0.97 V vs. RHE (reversible hydrogen electrode) in an H-cell. Notably, the Bi/OD-Cu electrode demonstrates an FE_formate of 95.8% at −0.97 V vs. RHE and a total current density close to 90 mA·cm⁻² at −1.17 V vs. RHE in a neutral flow cell. The experimental studies reveal that the remarkable CO₂RR performance of the Bi/OD-Cu results from the electron transfer from Cu to Bi, which optimizes adsorption of the CO₂^•− and boosts reaction kinetics. This study emphasizes the crucial role of substrate engineering strategies in enhancing catalytic activity and shows the possibility for a porous metal electrode in advancing the industrialization of formate production. Full article

Background: The innate immune response aims to prevent pathogens from entering the organism and/or to facilitate pathogen clearance. Innate immune cells, such as macrophages, mast cells (MCs), natural killer cells and neutrophils, bear pattern recognition receptors and are thus able to recognize common molecular patterns, such as pathogen-associated molecular patterns (PAMPs), and damage-associated molecular patterns (DAMPs), the later occurring in the context of neuroinflammation. An inflammatory component in the pathology of otherwise “primary cerebrovascular and neurodegenerative” disease has recently been recognized and targeted as a means of therapeutic intervention. Activated MCs are multifunctional effector cells generated from hematopoietic stem cells that, together with dendritic cells, represent first-line immune defense mechanisms against pathogens and/or tissue destruction. Methods: This review aims to summarize evidence of MC implication in the pathogenesis of neurodegenerative diseases, namely, Alzheimer’s disease, Parkinson’s disease, amyotrophic lateral sclerosis, Huntington’s disease, and multiple sclerosis. Results: In view of recent evidence that the gut–brain axis may be implicated in the pathogenesis of neurodegenerative diseases and the characterization of the neuroinflammatory component in the pathology of these diseases, this review also focuses on MCs as potential mediators in the gut–brain axis bi-directional communication and the possible role of Helicobacter pylori, a gastric pathogen known to alter the gut–brain axis homeostasis towards local and systemic pro-inflammatory responses. Conclusion: As MCs and Helicobacter pylori infection may offer targets of intervention with potential therapeutic implications for neurodegenerative disease, more clinical and translational evidence is needed to elucidate this field. Full article

With the development of electronic packaging technology toward miniaturization, integration, and high reliability, the diameter and pitch of solder joints continue to shrink. Adjacent solder joints are highly susceptible to electrochemical migration (ECM) due to the synergistic effects of high-density electric fields, water vapor, and contaminants. Dust has become one of the non-negligible causal factors in ECM studies due to air pollution. In this study, 0.2 mM/L NaCl and Na₂SO₄ solutions were used to simulate soluble salt in dust, and the failure mechanism of an Sn-58Bi solder ECM in the soluble salt in dust was analyzed by a water-droplet experimental method. It was shown that the mean failure time of the ECM of an Sn-58Bi solder in an NaCl solution (53 s) was longer than that in an Na₂SO₄ solution (32 s) due to the difference in the anodic dissolution characteristics in the two soluble salt solutions. XPS analysis revealed that the dendrites produced by the ECM process were mainly composed of Sn, SnO, and SnO₂, and there were precipitation products—Sn(OH)₂ and Na₂SO₄—attached to the dendrites. The corrosion potential in the NaCl solution (−0.351 V) was higher than that in the Na₂SO₄ solution (−0.360 V), as shown by a polarization test, indicating that the Sn-58Bi solder had better corrosion resistance in the NaCl solution. Therefore, an Sn-58Bi solder has better resistance to electrochemical migration in an NaCl solution compared to an Na₂SO₄ solution. Full article

FeCrMn_xAlCu (x = 2.0, 1.5, 1.0, 0.5, and 0.0) high-entropy alloys (HEAs) were prepared using vacuum arc melting. The phase structure, microstructure, and element distribution of FeCrMn_xAlCu (x = 2.0, 1.5, 1.0, 0.5, and 0.0) HEAs were analyzed using X-ray diffraction, scanning electron microscopy, and energy-dispersive spectroscopy. The corrosion resistance of the alloy in a NaOH solution was evaluated using a potentiodynamic polarization curve, electrochemical impedance spectroscopy, an immersion test, WLI, and X-ray photoelectron spectroscopy. The results showed that FeCrMn_xAlCu HEAs are an FCC+BCC bi-phase mixed structure with typical dendrite and interdendrite structures. The corrosion test demonstrated that the HEAs presented a breakthrough characteristic of activation–passivation–passivation. With an increase in Mn content, the corrosion potential shifted first positively and then negatively, and the corrosion current first decreased and then increased. Among HEAs, the FeCrMn_0.5AlCu HEA had the best electrochemical corrosion resistance. After corrosion, both oxide and hydroxide corrosion product films were formed on the surface, which reduced the ion diffusion rate, slowed down the corrosion process, and improved the corrosion resistance. Full article

High ionic conductivity, outstanding mechanical stability, and a wide electrochemical window are the keys to the application of solid-state lithium metal batteries (LMBs). Due to their regular channels for ion transport and tailored functional groups, covalent organic frameworks (COFs) have been applied to solid electrolytes to improve their performance. Herein, we report a flexible polyethylene oxide-COF-LZU1 (abbreviated as PEO-COF) electrolyte membrane with a high lithium ion transference number and satisfactory mechanical strength, allowing for dendrite-free and long-time cycling for LMBs. Benefiting from the interaction between bis(triflfluoromethanesulonyl)imide anions (TFSI⁻) and aldehyde groups in COF-LZU1, the Li⁺ transference number of the PEO-5% COF-LZU1 electrolyte reached up to 0.43, much higher than that of neat PEO electrolyte (0.18). Orderly channels are conducive to the homogenous Li-⁺ deposition, thereby inhibiting the lithium dendrites. The assembled LiFePO₄|PEO-5% COF-LZU1/Li cells delivered a discharge specific capacity of 146 mAh g⁻¹ and displayed a capacity retention of 80% after 200 cycles at 0.1 C (60 °C). The Li/Li symmetrical cells of the PEO-5% COF-LZU1 electrolyte presented a longer working stability at different current densities compared to that of the PEO electrolyte. Therefore, the enhanced comprehensive performance of the solid electrolyte shows potential application prospects for use in LMBs. Full article

Sodium batteries are receiving increasing interest as an alternative to reduce dependence on lithium-based systems. Furthermore, the development of solid-state electrolytes will lead to higher-performing and safer devices. In this work, a Zn-based metal–organic framework (Zn-MOF-74) is combined as a physical barrier against the growth of dendrites, together with 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([EMIm][TFSI]) ionic liquid, which provides improved mobility to sodium ions. It is demonstrated that the incorporation of the appropriate amount of ionic liquid within the pores of the MOF produces a considerable increase in ionic conductivity, achieving values as high as 5 × 10⁻⁴ S cm⁻¹ at room temperature, in addition to an acceptable Na⁺ transference number. Furthermore, the developed Na[EMIm][TFSI]@Zn-MOF-74 hybrid solid electrolyte contributes to stable and dendrite-free sodium plating/stripping for more than 100 h. Finally, a more than notable extension of the electrochemical stability window of the electrolyte has been determined, being useful even above 7 V vs. Na⁺/Na. Overall, this work presents a suitable strategy for the next generation of solid-state sodium batteries. Full article

To reduce the use of the toxic Pb element in the Cu-Sn alloy with high friction performance, Cu-xBi-10Sn alloys with different Bi contents were prepared by gravity casting, and the effect of Bi content on the microstructure, mechanical properties and wear property of Cu-Sn alloys were studied. The results showed that the Bi element was distributed in bands or long strips on the dendritic arms and did not form compounds with other elements. With the increase in Bi content, the hardness and tensile strength of Cu-xBi-10Sn alloys present a trend of increasing first and then decreasing. When the Bi content was 7 wt.%, the maximum hardness value was obtained, and the ultimate tensile strength was close to that of Cu-10Pb-10Sn alloy. Compared with Cu-10Pb-10Sn alloy, Cu-7Bi-10Sn alloy also possessed better friction reduction and wear resistance under the oil lubrication condition. Full article

In this study, robust composite solid electrolytes were developed and employed to enhance the performance of Li-metal batteries significantly. The robust composite solid electrolytes are composed of a soft polymer, poly(ethylene oxide), a Li salt, bis(trifluoromethanesulfonyl)imide (LiTFSI), and super ionic conductive ceramic fillers such as Li_1.5Al_0.5Ti_1.5(PO₄)₃ (LATP), and Li_6.4La₃Zr_1.4Ta_0.6O₁₂ (LLZTO). The main goal of this study is to enhance the electrochemical stability and ionic conductivity. The ionic conductivities of the composite solid electrolytes were found to be 2.08 × 10⁻⁴ and 1.64 × 10⁻⁴ S cm⁻¹ with the introduction of LATP and LLZTO fillers, respectively. The results prove that the fabricated solid electrolyte was electrochemical stable at voltage exceeding 4.25 V vs. Li/Li⁺. The internal resistance of the solid electrolyte significantly reduced compared to gel electrolyte. This reduction can be attributed to the alleviation of bulk electrolyte, charge-transfer, and interfacial electrolyte/electrode impedance. When LiFePO₄ cathode sheets are coated with a composite solid electrolyte containing LATP powders, the resulting Li-metal battery displays high capacity at 5 C (with a capacity retention of 65.2% compared to the original capacity at 0.2 C) as well as superior cyclic stability and excellent Coulombic efficiency (>99.5%, 200 cycles). These results confirm that the composite solid electrolyte acts as a protective layer which has the ability to prevent the growth of Li dendrites. Consequently, the fabricated electrolyte configuration can be engineered to enable high energy/power density and electrochemical stable cyclability in Li-metal batteries. Full article

Dendrite growth and parasitic reactions with liquid electrolyte are the two key factors that restrict the practical application of the lithium metal anode. Herein, a bis(benzene sulfonyl)imide based single-ion polymer artificial layer for a lithium metal anode is successfully constructed, which is prepared via blending the as-prepared copolymer of lithiated 4, 4′-dicarboxyl bis(benzene sulfonyl)imide and 4,4′-diaminodiphenyl ether on the surface of lithium foil. This single-ion polymer artificial layer enables compact structure with unique continuous aggregated Li⁺ clusters, thus reducing the direct contact between lithium metal and electrolyte simultaneously, ensuring Li⁺ transport is fast and homogeneous. Based on which, the coulombic efficiency of the Li|Cu half-cell is effectively improved, and the cycle stability of the Li|Li symmetric cell can be prolonged from 160 h to 240 h. Surficial morphology and elemental valence analysis confirm that the bis(benzene sulfonyl)imide based single-ion polymer artificial layer effectively facilitates the Li⁺ uniform deposition and suppresses parasitic reactions between lithium metal anode and liquid electrolyte in the LFP|Li full-cell. This strategy provides a new perspective to achieve a steady lithium metal anode, which can be a promising candidate in practical applications. Full article

Anode-less sodium metal batteries have drawn dramatica attention owing to their high specific energy and low cost. However, the growth of sodium dendrites and the resulting loss of active materials and serious safety concerns hinder their practical applications. In this work, a bismuth-based modification layer with good sodiophilicity is constructed on the surface of Cu foil (denoted as Cu@Bi) to control the deposition of Na metal. The activation-derived porous Na-rich alloy phase can provide abundant nucleation sites and reduce the nucleation overpotential to induce the uniform and dense deposition of Na metal. When evaluated in half cell, the Cu@Bi current collectors can operate for 750 h at 1 mA cm⁻² and 1 mAh cm⁻², with an average coulombic efficiency (CE) of 99.5%. When the current density is improved to 2 mA cm⁻², the Cu@Bi can also stably maintain for 750 cycles, demonstrating the remarkable effect of the modification layer. When coupled with the Na₃V₂(PO₄)₃ cathode, the full cell exhibits stable cycle performance over 80 cycles. The modification strategy of alloy modification can provide fresh ideas for the research and application of anode-less and even anode-free metal batteries. Full article

Chromatin regulators (CRs) are essential upstream regulatory factors of epigenetic modification. The role of CRs in the pathogenesis of renal ischemia-reperfusion injury (IRI) remains unclear. We analyzed a bioinformatic analysis on the differentially expressed chromatin regulator genes in renal IRI patients using data from public domains. The hub CRs identified were used to develop a risk prediction model for renal IRI, and their expressions were also validated using Western blot, qRT-PCR, and immunohistochemistry in a murine renal IRI model. We also examined the relationships between hub CRs and infiltrating immune cells in renal IRI and used network analysis to explore drugs that target hub CRs and their relevant downstream microRNAs. The results of machine learning methods showed that five genes (DUSP1, GADD45A, GADD45B, GADD45G, HSPA1A) were upregulated in renal IRI, with key roles in the cell cycle, p38 MAPK signaling pathway, p53 signaling pathway, FoxO signaling pathway, and NF-κB signaling pathway. Two genes from the network, GADD45A and GADD45B (growth arrest and DNA damage-inducible protein 45 alpha and beta), were chosen for the renal IRI risk prediction model. They all showed good performance in the testing and validation cohorts. Mice with renal IRI showed significantly upregulated GADD45A and GADD45B expression within kidneys compared to sham-operated mice. GADD45A and GADD45B showed correlations with plasmacytoid dendritic cells (pDCs) in infiltrating immune cell analysis and enrichment in the MAPK pathway based on the weighted gene co-expression network analysis (WGCNA) method. Candidate drugs that target GADD45A and GADD45B include beta-escin, sertraline, primaquine, pimozide, and azacyclonol. The dysregulation of GADD45A and GADD45B is related to renal IRI and the infiltration of pDCs, and drugs that target GADD45A and GADD45B may have therapeutic potential for renal IRI. Full article