Search Results (106)

Impaired wound healing arises from interacting biological and material challenges, including persistent infection, biofilm formation, oxidative stress, unresolved inflammation, impaired angiogenesis, defective epithelialization, hemorrhage, and insufficient real-time assessment of wound status. Quantum dot (QD) and nanodot nanosystems have emerged as a versatile class of bioactive wound interfaces capable of addressing these barriers through functions that extend beyond passive coverage. This review synthesizes the design rationale, material composition, validation strategies, functional outcomes, mechanistic interpretation, and translational relevance of QD-enabled platforms for precision wound repair. Across the reviewed literature, carbon dots, graphene QDs, black phosphorus QDs, metal and metal oxide QDs, transition-metal nanodots, and hybrid nanocomposites were incorporated into hydrogels, films, sponges, nanofibers, microneedles, scaffolds, membranes, sprays, and injectable matrices. Their major precision-enabling attributes include localized antimicrobial and antibiofilm activity, redox-adaptive behavior, photothermal and photodynamic activation, inflammatory and macrophage modulation, hemostasis, controlled therapeutic delivery, angiogenic and epithelial support, and fluorescence-based monitoring. The strongest conceptual advance is the transition from static wound dressings toward adaptive biointerfaces that can sense, respond to, or compensate for local wound state abnormalities. Nevertheless, the field remains largely preclinical, with important gaps in long-term safety, standardized characterization, clinically predictive models, manufacturing reproducibility, regulatory alignment, and human validation. Future progress will depend on rationally simplified multifunctional platforms, rigorous comparative testing, wound state-specific evaluation frameworks, and translation-oriented safety and usability studies. QD nanosystems therefore represent a promising foundation for precision wound repair, provided that their multifunctionality is matched by equally rigorous evidence of safety, reproducibility, and clinical relevance. Full article

The development of highly efficient, stable, and cost-effective non-precious metal electrocatalysts to replace conventional platinum-based materials holds profound significance for accelerating the commercialization of advanced energy conversion devices, such as zinc–air batteries (ZABs). Herein, we propose a facile and highly efficient strategy to prepare a defect-rich, highly active nitrogen-doped porous carbon-based electrocatalyst (denoted U-Fe-N-C, urea-assisted iron–nitrogen–carbon material), via high-temperature co-pyrolysis of heme with urea. Our results demonstrate that urea not only serves as an excellent nitrogen source during pyrolysis, introducing abundant topological defects and heteroatom doping sites, but also induces the carbon substrate to form a hierarchical sponge-like porous structure with a high specific surface area. This unique microenvironment effectively prevents the agglomeration of iron species at high temperatures, achieving enhanced dispersion of iron species stabilized within the nitrogen-rich carbon matrix. Electrochemical evaluations reveal that under the optimal synthesis conditions (a precursor mass ratio of 1:3, calcination at 900 °C), U-Fe-N-C exhibits excellent oxygen reduction reaction (ORR) catalytic performance, delivering a half-wave potential of 0.731 V vs. RHE, and shows long-term operational durability that significantly surpasses that of commercial Pt/C. Furthermore, liquid rechargeable zinc–air batteries assembled with U-Fe-N-C as the air cathode deliver remarkable cycling stability, operating for up to 270 h of charge–discharge cycling without noticeable performance degradation. This study not only provides useful insights into the mechanisms of pore formation and assistance but also offers a practical perspective for the rational design and scalable synthesis of high-performance metal–nitrogen–carbon (M-N-C) electrocatalysts. Full article

As a widely used sponge facility, the permeable pavement system (PPS) frequently exhibited a decline in pollutant removal after long-term operation. However, the long-term impacts of different cushion fillers on pollutant removal and ecological risk remain unclear. This study modified a conventional sand-based PPS (S1) by replacing the cushion layer with five materials: construction waste bricks (S2), coal gangue (S3), activated carbon (S4), carbon nanotubes (S5), and graphene (S6). A 5-year laboratory experiment evaluated the removal efficiency, fraction distribution, and ecological risk of heavy metals (HMs: Mn, Pb, Zn, Cu, Cd, Ni) from rainfall. The key findings demonstrated significant variations among fillers. S2 showed the poorest performance with a removal efficiency of 83.26% ± 13.02 across all HMs, whereas carbonaceous-modified systems (S4–S6) exhibited high removal efficiencies, exceeding 97.00% ± 1.89. Residual and Fe/Mn oxide states were predominant among the HMs, exceeding 43.69%, indicating enhanced metal immobilization. The ecological risks of carbon nanotubes and graphene were the highest, with risk indices of 1123.02 and 1129.63, respectively. These findings demonstrated that carbonaceous fillers achieved superior HM sequestration, leading to an overall reduction in ecological risk in the effluent of PPS after long-term operation. Overall, this study provided new perspectives on elucidating long-term removal efficiency and the ecological risk mitigation of PPS, and supported future application of carbonaceous fillers in sustainable PPS design and construction. Full article

Lithium-ion batteries have been widely used as energy storage and power batteries due to their unique advantages. However, with increasing demands for battery performance and application scenarios, battery safety has become a significant obstacle to their application. To address this issue, this paper proposes and fabricates an advanced polyimide (PI) separator material with high porosity and excellent thermal stability. By introducing sodium chloride (NaCl) as a pore-forming template into a polyamic acid (PAA) precursor, a PI-based separator with a uniformly interpenetrating sponge-like pore structure was successfully constructed. The obtained PI-NaCl separator exhibits outstanding thermal structural stability, maintaining dimensional integrity without significant thermal shrinkage even when tested at temperatures as high as 250 °C. Furthermore, the porous structure of the PI-NaCl separator demonstrates excellent electrolyte wettability, as the electrolyte rapidly spreads upon contact (contact angle approaching 0°), which is significantly superior to commercial separators. In lithium symmetric cell tests, this separator achieves long-term stable stripping/plating cycling by virtue of its outstanding ionic conductivity, effectively mitigating interfacial side reactions with lithium metal. In LiFePO₄||C full-cell applications, the PI-NaCl-based battery exhibits good rate capability and cycling stability. Additionally, in an open-circuit voltage (OCV) monitoring experiment at a high temperature of 80 °C, the voltage of the PI-NaCl-based battery remained stable continuously for 8 h in comparison to that of the commercial separator-based battery. Full article

High-performance polyethersulfone (PES) ultrafiltration membranes integrating antibacterial activity and antifouling performance were fabricated via the in situ construction of bimetallic polyphenol networks (BMPNs) throughout the membrane architecture. Tannic acid (TA) functioned as a multifunctional molecular bridge, functionalizing silver metal–organic frameworks (Ag-MOFs) to yield hydrophilic T-Ag-MOFs and chelating Fe³⁺ ions from the coagulation bath to form a polyphenol network during phase inversion. T-Ag-MOF incorporation generated asymmetric morphologies featuring highly porous surfaces and sponge-like cross-sections, improving pure water permeability, mechanical integrity, and bovine serum albumin (BSA) rejection. TA-mediated functionalization increased hydrophilicity, imparted a negative surface charge, suppressed nonspecific protein adhesion, and enhanced flux recovery with low irreversible fouling. At an optimal loading of 0.4 wt%, the resultant T-Ag-MOF/Fe³⁺/PES composite membrane achieved a pure water permeability of 593.4 L m⁻² h⁻¹ bar⁻¹—1.77-fold higher than that of the pristine PES control—while sustaining a BSA rejection of 96.5%. Notably, interfacial compatibility between the T-Ag-MOFs and PES matrix was enhanced, facilitating strong, covalent-like filler–matrix adhesion. Moreover, the composite membrane delivered synergistic multifunctionality, including exceptional long-term aqueous stability, precisely tuned Ag⁺ release kinetics, and potent antibacterial activity, as evidenced by negligible uncontrolled ion leaching and a lack of structural degradation under prolonged hydration. Full article

Solar interfacial evaporation is promising for freshwater production, yet thermodynamic energy limits and mass transfer attenuation in high-salinity environments restrict practical applications. To address these challenges, a 3D high-efficiency evaporator is developed by cross-linking a hydrophilic composite gel onto a macroporous sponge scaffold. This spatially decoupled architecture enables fundamental water-state regulation and efficient environmental heat harvesting. Specifically, hydrophilic functional groups in the gel network reduce the equivalent enthalpy of vaporization of water to 1181.8 J g⁻¹. Simultaneously, the 3D columnar structure induces a sidewall cold sink effect to extract additional ambient thermal energy. Through this synergy, the PCPH delivers a remarkable apparent evaporation rate of 8.59 kg m⁻² h⁻¹ under one standard sun. Furthermore, interconnected macropores within the sponge establish excellent convective pathways for rapid ion diffusion. Consequently, the device operated continuously for 8 h in a 10 wt% NaCl solution without significant blockage and decreased key metal ion concentrations in 3.5 wt% simulated seawater by 4 to 5 orders of magnitude. The purified water fully satisfies World Health Organization standards. This study offers an innovative strategy to surpass conventional photothermal bottlenecks and design highly durable water treatment materials. Full article

The Rio Grande Rise (RGR) is the largest oceanic plateau in the South Atlantic and represents a key natural laboratory for understanding oceanic plateau formation, deep-sea circulation, ecosystem functioning, and ferromanganese crust development. This study presents a critical synthesis of current scientific knowledge on the RGR, integrating geological, geophysical, oceanographic, biological, and geochemical evidence published over the last two decades. Geophysical data reveal a complex tectono-magmatic evolution involving Late Cretaceous plume-related volcanism, crustal thickening, rifting, and subsequent subsidence. The structural framework of the plateau is dominated by the Cruzeiro do Sul Rift, which plays a central role in controlling sedimentation, magmatism, and seawater circulation. Oceanographic studies demonstrate that the interaction between the southern branch of the South Equatorial Current and the complex topography of the RGR generates intense internal tides and bottom currents, strongly influencing sediment transport and benthic habitats. Biological investigations indicate that the RGR hosts diverse deep-sea communities, including sponge grounds, cold-water corals, and associated fauna, whose distribution is tightly linked to geomorphology and hydrodynamics. Ferromanganese crusts occurring on the plateau preserve valuable geochemical records of oceanographic and redox conditions, although their spatial distribution, thickness, and metal budgets remain incompletely constrained. Despite major advances, significant knowledge gaps persist regarding crustal structure, sedimentary evolution, ecosystem functioning, and mineral formation processes. This review highlights these uncertainties and outlines research priorities necessary to improve understanding of oceanic plateaus and deep-sea systems in the South Atlantic. Full article

Porous Ca₂Mg₂Al₂₈O₄₆ (C₂M₂A₁₄) ceramics are highly competitive candidates in the field of critical metal filtration due to their attractive non-metallic-inclusions removal capacity. However, the low mechanical strength and inadequate thermal shock resistance (TSR) of these materials restrict their further application. In this work, ZrO₂-toughened C₂M₂A₁₄-based porous ceramics are fabricated by using the polymer sponge replica method. Nano-sized ZrO₂ particles derived from nano-ZrO₂ sol are beneficial to enhance the mechanical properties and TSR of porous ceramics. The optimized porous C₂M₂A₁₄ ceramics exhibit robust compressive strength (2.15 MPa), good residual strength ratio (66.4%) and excellent filtration efficiency in the reduction in total oxygen content (68.4%) by adding 3 wt% ZrO₂ sol. These excellent comprehensive properties show that as-prepared porous C₂M₂A₁₄ ceramics are promising candidate materials for application in the field of critical metal filtration. Full article

In this study, the metallic Y, CaF₂, and sponge Ti were employed to regulate the composition and achieve the deoxidation of the SHS-TiAl alloy, respectively. The results indicate that the metallic Y could effectively reduce the oxygen concentration of the SHS-TiAl alloys, which could all be controlled below 0.06 wt.%. The alloying control of SHS-TiAl could be further realized by adding sponge Ti with the achievement of a typical α + γ phase microstructure. Additionally, the CaF₂ could adsorb the Y₂O₃ products, which were formed during the deoxidation reaction. However, due to the relatively high initial oxygen content in the SHS-TiAl alloy, the generated Y₂O₃ could not be fully removed, leading to the partial inclusions remaining in the alloy matrix. Also, the residual Y would react with Al in the alloy to form YAl₂ inclusions. Full article

This experimental review discusses evolutionarily approved, naturally pre-designed skeletal architectures of marine keratosan sponges in the form of 3D scaffolds, which have garnered increasing interest in the fields of structural and functional biomimetics as well as in tissue engineering. It has been demonstrated that these renewable, ready-to-use natural scaffolds can undergo further modifications through specialized treatments such as metallization and carbonization, enabling the creation of functional biomaterials while maintaining the species-specific hierarchical 3D structure. The study presented remarkable findings, including the demonstration of the unique shape-memory behavior of these scaffolds even after two months of exposure to high mechanical pressure at temperatures exceeding 100 °C. Additionally, the cytocompatibility and biological performance of natural and carbonized (1200 °C) spongin scaffolds, derived from selected bath sponges, were comparatively investigated with respect to growth and proliferation of human MG-63 osteoblastic cells. Understanding whether carbonization universally enhances osteogenic capabilities or selectively amplifies the inherent architectural advantages remains to be critical for the rational design of sponge-derived scaffolds in bone and structural tissue engineering applications. Full article

Chitosan is a natural biopolymer for advanced wound healing due to its antimicrobial activity, biocompatibility, and hemostatic properties. However, its clinical utility is limited by its low solubility and poor mechanical properties. This review summarizes recent strategies that have successfully overcome these shortcomings, focusing on the development of multifunctional chitosan hybrid dressings. These dressings, which include hydrogels, hydrocolloids, films, sponges, and scaffolds, are now being fabricated using advanced systems like electrospinning, 3D printing, microneedle (MN), and nanocomposites technologies to maximize wound healing efficacy. Specifically, modification techniques used to overcome chitosan’s shortcomings include: (1) chemical derivatization to enhance solubility, (2) polymer hybridization with natural and synthetic materials to enhance mechanical properties, and (3) functionalization with active ingredients. These materials, including metal/inorganic nanoparticles, natural compounds, and amino acids, are added to maximize therapeutic efficacy. In conclusion, chitosan hybrid materials and dressings provide an excellent foundation for next-generation wound dressings. However, overcoming challenges associated with material diversity and establishing standardized manufacturing processes and clinical trials remain critical for successful commercialization. Full article

Four new porous homochiral metal–organic frameworks (MOFs), [M₂(camph)₂(bpa)]∙Solv (M = Co(II), Ni(II), Cu(II) and Zn(II)), based on (+)-camphoric acid (H₂camph) and 1,2-bis(4-pyridyl)ethane (bpa) were synthesized and characterized. The crystal structures of [Ni₂(camph)₂(bpa)] and [Zn₂(camph)₂(bpa)] were established by single-crystal X-ray diffraction analysis. Powder X-ray data prove the phase purity and isostructural nature of all four compounds. The thermal stability of [M₂(camph)₂(bpa)] was found to depend on the electronic configuration, as well as on the redox properties of the metal cation, and varied from 225 °C (M = Zn²⁺) to 375 °C (M = Ni²⁺). The reversible, solvent-induced sponge-like dynamics of the coordination frameworks was thoroughly investigated. Changes in the positions of reflexes, related to the length of the flexible bpa linker, were observed by powder XRD, pointing to transitions between an open-framework phase and a squeezed, non-porous phase in a crystal-to-crystal manner, while the integrity and connectivity of the coordination network were maintained. Size-selective adsorption from a benzene–cyclohexane 1:1 mixture on [Zn₂(camph)₂(bpa)] was studied by ¹H NMR analysis. The benzene-favorable composition of guest molecules (C₆H₆:C₆H₁₂ = 5:1) occluded within the host crystalline sponge revealed a preferable adsorption affinity towards smaller benzene compared with larger cyclohexane. High framework stability in various solvents, as well as successful molecular separation in the liquid state, validates the potential utilization of chiral porous metal(II) camphorate MOFs in important stereoselective applications. Full article

Basalt fiber reinforced polymer (BFRP) is one of the new materials that can be used for making photovoltaic scaffolds, which can effectively solve the problem of the rapid deterioration of complex environmental performance and high maintenance cost of traditional scaffold materials. This paper focuses on the BFRP photovoltaic support in the cold and arid irrigation area of northwest China, carries out the durability test under the action of chloride salt, freeze-thaw cycle, and chloride salt freeze-thaw environment coupling, and it compares and analyzes the degradation law of the mechanical properties of BFRP sheets under different environmental effects. The performance degradation mechanism of BFRP materials under different environmental effects was revealed by SEM scanning electron microscopy and EDS energy spectrum analysis. The main conclusions are as follows: (1) Under the action of chloride salt, the tensile strength, elastic modulus and elongation at break of the specimen decreased by 11.46%, 7.02%, and 10.27%, respectively. Under the freeze-thaw cycle, the tensile strength and elongation at break of the specimen decreased by 9.62% and 6.85%, while the elastic modulus first increased and then decreased, with a maximum decrease of 12.95%. The degradation of mechanical properties is the most serious under the coupling effect of chloride salt and the freeze-thaw environment. The tensile strength, elastic modulus, and elongation at break of the specimens decreased by 25.73%, 9.55%, and 24.81%, respectively. (2) In the chloride environment, the distribution of elements on the surface of the specimen changed, the metal ions of the fibers precipitated, and ‘black spots‘ and corrosion pits appeared. The resin matrix forms ‘sponge-like‘ pores; under the freeze-thaw cycle, the fiber–resin interface cracks and fiber shedding intensifies; under the coupling effect of chloride freeze-thaw, ‘black spots‘, pits, resin holes, and interface cracks increased, and chloride penetration corrosion accelerated. Full article

The efficient degradation of antibiotics in pharmaceutical wastewater remains a critical challenge against environmental contaminants. Conventional photocatalysts face potential limitations such as narrow visible-light absorption, rapid carrier recombination, and reliance on precious metal cocatalysts. This review investigates the coordination structure of MXene as a cocatalyst to synergistically enhance photocatalytic antibiotic degradation efficiency and the coordination structure modification mechanisms. MXene’s tunable bandgap (0.92–1.75 eV), exceptional conductivity (100–20,000 S/cm), and abundant surface terminations (-O, -OH, -F) enable the construction of Schottky or Z-scheme heterojunctions with semiconductors (Cu₂O, TiO₂, g-C₃N₄), achieving 50–70% efficiency improvement compared to pristine semiconductors. The “electron sponge” effect of MXene suppresses electron-hole recombination by 3–5 times, while its surface functional groups dynamically optimize pollutant adsorption. Notably, MXene’s localized surface plasmon resonance extends light harvesting from visible (400–800 nm) to near-infrared regions (800–2000 nm), tripling photon utilization efficiency. Theoretical simulations demonstrate that d-orbital electronic configurations and terminal groups cooperatively regulate catalytic active sites at atomic scales. The MXene composites demonstrate remarkable environmental stability, maintaining over 90% degradation efficiency of antibiotic under high salinity (2 M NaCl) and broad pH range (4–10). Future research should prioritize green synthesis protocols and mechanistic investigations of interfacial dynamics in multicomponent wastewater systems to facilitate engineering applications. This work provides fundamental insights into designing MXene-based photocatalysts for sustainable water purification. Full article

Marine-derived Actinomycetota have emerged as promising sources of bioactive natural products, particularly filamentous actinomycetes (e.g., Streptomyces). However, members from non-filamentous genera have showed potential biotechnological importance. In this study, we performed a comprehensive genomic characterization of two bioactive Brevibacterium strains, Brevibacterium luteolum (B. luteolum) 26C and Brevibacterium casei (B. casei) 13A, isolated from two Red Sea sponges. Whole-genome sequencing and taxonomic analysis confirmed species-level identification, marking the first documented report of these species within the Red Sea ecosystem. The two strains displayed antimicrobial activity against Staphylococcus aureus, Escherichia coli, and Candida albicans. Additionally, functional annotation revealed multiple genomic islands (GIs) enriched with genes conferring heavy metal resistance, DNA repair enzymes, nutrient acquisition, and mobile genetic elements, highlighting potential evolutionary adaptations to the harsh physicochemical conditions of the Red Sea. Genome mining identified biosynthetic gene clusters, including those encoding ε-poly-L-lysine, tropodithietic acid, ectoine, and carotenoids. The comparative analysis of orthologous gene clusters from both strains and their counterparts from terrestrial ecosystems highlighted potential marine adaptive genetic mechanisms. This study highlights the biosynthetic potential of B. luteolum 26C and B. casei 13A and their ecological role as active competitors and potential defensive associates within the sponge microbiome. Full article