Search Results (4,567)

Self-sustained metal aerogels are emerging as advanced porous materials with a 3D network of nanostructures that are exclusively made of metals. Metal aerogels possess a distinctive combination of metallic nanoparticles with excellent electronic conductivity, and the excellent porosity of the aerogels allows the extensive exposure of electrocatalytic active sites, together with remarkable mass transport networks in a single entity, unlocking widespread application potential ranging from energy storage and conversion to environmental remediation. In this review, we systematically examine the potential of metal aerogels as electrocatalysts for ethanol electro-oxidation. Various synthesis routes, structure–property relationships, and their function as anode electrocatalysts have been critically reviewed. Due to their 3D porous metallic nature, noble metal aerogel catalysts were found to exhibit excellent ethanol oxidation currents, anti-poisoning for reaction intermediates, high mass, and specific activities of 5–20 times those of traditional Pd/C catalysts. In conclusion, it is shown that metal aerogel catalysts exhibit enhanced activity for ethanol electro-oxidation currents over traditional Pd/C catalysts. Despite this, several challenges exist in realizing the commercial applications of metal aerogels, which have been clearly and elaborately stated as future perspectives and research directions in the field of metal aerogel electrocatalysis. Full article

Innovations in nanomaterial science, engineering and printing technologies have increasingly driven advances in electrochemical sensing. Screen-printed electrodes (SPEs) have become a versatile, low-cost, and scalable solution for developing portable electrochemical detection platforms. However, their analytical performance remains intrinsically limited by surface area, electron transfer efficiency, and the immobilization of biomolecules. Recent developments in nanostructured materials, ranging from two-dimensional (2D) materials such as graphene, MXenes, and transition metal dichalcogenides, to one-dimensional nanostructures and hybrid nanocomposites, have transformed the signal transduction landscape of SPE-based electrochemical sensors. Integration of nanomaterials into SPEs has successfully transformed their analytical capabilities, but the diversity of materials and modification strategies has made it difficult to consolidate current knowledge in the field. Strategies that integrate nanomaterials via ink formulation, surface modification, or in situ growth have yielded sensors with unprecedented sensitivity, reproducibility, and selectivity across various chemical and biological targets. This review offers a cross-material synthesis of how nanomaterial engineering transforms the electrochemical performance of SPEs. By integrating insights across morphology, interfacial chemistry, and device-level behavior, it establishes a unified perspective that has been missing from the current literature and clarifies the design principles driving next-generation SPE-based sensing platforms. Full article

The production of green hydrogen via aqueous electrolysis of hydrogen sulfide (H₂S) holds significant potential to address challenges related to sustainable energy generation and environmental protection. The electrocatalytic splitting of water polluted with highly toxic H₂S is attractive for industrial applications because the process: (i) is less power-consuming than direct thermal H₂S decomposition; (ii) achieves high Faradaic efficiencies for hydrogen production; and (iii) yields elemental sulfur as an added-value by-product. This review covers a brief discussion on sulfide-containing water sources and electrochemical methods for hydrogen production from H₂S, specifically Direct, Indirect, and Electrochemical Membrane Reactor (EMR) systems. To become commercially and economically attractive, these approaches require improvements in electrolysis efficiency through the development of low-cost electrode materials that are resistant to sulfur poisoning and corrosion, while possessing high catalytic activity, enhanced stability, and durability. Early research focused on carbon-based materials combined with noble metal oxides, transition metal compounds, and related materials. Since their practical performance is limited, investigations have shifted toward nanostructured electrocatalysts with unique crystal structures and designs, which show significantly improved efficiency for H₂S electrolysis. This review highlights the potential of H₂S electrolysis for hydrogen production, giving special attention to recent advancements in electrode materials. Full article

Wood coatings play a critical role in protecting wood substrates from environmental degradation, particularly ultraviolet (UV)-induced photodegradation. This review comprehensively examines the mechanisms of wood coating photodegradation, the factors influencing their durability, and current anti-aging strategies. Photodegradation arises from polymer chain scission, chemical structure reorganization, and photo-oxidation of lignin and cellulose, leading to coating chalking, cracking, gloss loss, and color changes, ultimately compromising wood mechanical properties and service life. Key anti-aging strategies include UV absorbers, which convert harmful UV radiation into heat; hindered amine light stabilizers (HALSs) that capture free radicals and quench excited-state molecules; barrier and shielding materials that form dense physical or nanostructured networks to block UV penetration and enhance mechanical and water resistance; and antioxidants that neutralize free radicals or decompose peroxides at the molecular level. Each approach can be employed individually or synergistically to enhance coating durability. Challenges remain in achieving long-term outdoor stability, balancing transparency and UV shielding, optimizing nanoparticle dispersion, and maintaining the activity of natural antioxidants. Future research should focus on multifunctional composite coatings integrating bio-based materials and nanotechnology, smart responsive systems, adaptive protection mechanisms, and standardized long-term evaluation protocols. These advancements will facilitate the development of high-performance, sustainable wood coatings and promote the value-added utilization of wood resources. Full article

With the rapid advancement of artificial intelligence and wearable technologies, the demand for soft, multifunctional electronic materials has grown substantially. Hydrogels have emerged as a promising platform due to their intrinsic softness, stretchability, and biocompatibility. Among them, cellulose-based conductive hydrogels uniquely integrate the sustainability of natural polymers with tunable electrical functionality, offering significant potential for flexible and biointegrated electronics. This review provides a comprehensive and critical perspective on the recent progress in cellulose-based conductive hydrogels. We systematically summarize key design strategies, including physical and chemical crosslinking and interpenetrating network engineering. More importantly, we present a comparative analysis of distinct conductive mechanisms, including ionic conduction, conductive polymers, metallic nanostructures, and carbon-based fillers, highlighting the inherent trade-offs among electrical conductivity, mechanical robustness, and environmental stability. Emerging applications in flexible electronics, energy storage, bioelectronics, and self-powered systems are discussed through structure–property relationships. Finally, we outline current challenges and future directions, emphasizing multifunctional integration, scalable fabrication, and long-term operational stability, thereby providing a framework for the rational design of next-generation sustainable electronic materials. Full article

This study investigates the effect of complex nanomodification combined with the simultaneous application of magnetic fields and mechanical vibration on the structure formation and performance properties of medium-alloy steel 40CrNi3MoV. Improving the structural homogeneity and operational characteristics of such steels remains an important task due to their widespread use in components operating under severe loading and wear conditions. The introduction of the nanostructured modifier InSteel-7 at a concentration of 0.03%, together with simultaneous magnetic and vibrational treatment of the melt, resulted in pronounced structural homogenization and grain refinement. Quantitative metallographic analysis using Thixomet Pro image analyzer revealed a significant refinement of the dendritic structure, with the secondary dendrite arm spacing decreasing from 73.9 μm to 27.9 μm. X-ray phase analysis confirmed the preservation of phase composition while indicating increased structural uniformity of the BCC matrix. Energy-dispersive spectroscopy and elemental micro-mapping demonstrated high chemical purity of the alloy and a uniform distribution of the modifier components. The combined treatment significantly improved the mechanical and tribological characteristics of the material. The average hardness increased from 390 HV to 510 HV, while tribological tests showed a reduction in wear track depth from 5.16 μm to 0.87 μm and a decrease in surface roughness from Ra 2.13 μm to 0.20 μm, indicating enhanced wear resistance. Full article

Access to clean water remains a critical global challenge, particularly in arid and fog-rich regions where conventional resources are limited. Fog water harvesting has emerged as a low-energy alternative; however, the performance of traditional collectors (typically 3–10 L m⁻² day⁻¹) remains constrained by inefficient droplet capture and transport. This review provides a systematic and critical analysis of recent advances in membrane-based fog harvesting technologies, focusing on material design, surface engineering, and structural optimization. The analysis shows that nanostructured and electrospun membrane systems can enhance water collection rates to ~20–60 L m⁻² day⁻¹, representing up to a 5–6 times improvement over conventional meshes. Furthermore, biomimetic and Janus wettability designs significantly improve droplet nucleation and directional transport, while hierarchical micro/nanostructures accelerate coalescence and runoff dynamics. At the structural level, optimized collector geometries (vertical harp designs) demonstrate ~3–4 times higher collection efficiency compared to traditional Raschel mesh due to reduced clogging and enhanced drainage. Despite these advances, key challenges remain, including material durability, fouling resistance, lack of standardized testing protocols, and limited large-scale validation. This review identifies critical design–performance relationships and proposes a framework linking surface wettability, morphology, and environmental parameters to harvesting efficiency. Future directions emphasize the development of durable, scalable membrane systems and the integration of fog harvesting with hybrid water supply technologies. Full article

The development of high-performance electrode materials with controlled morphology remains a key challenge for advancing supercapacitor technologies. In this study, polyethylene glycol (PEG)-assisted hydrothermal synthesis was employed to engineer NiCo₂S₄ nanostructures with controlled morphology for enhanced supercapacitor performance. The influence of PEG concentration on nucleation behavior, structural evolution, and electrochemical characteristics was systematically investigated. The optimized NiCo₂S₄ electrode synthesized with 0.2% PEG (NiCoS-P2) exhibited a hierarchical flower-like nanosheet architecture with reduced agglomeration and improved electrochemically accessible surface area. As a result, the electrode delivered a high areal capacitance of 13.689 F/cm² (specific capacitance of 6845 F/g) at 5 mA/cm², along with excellent rate capability and superior cycling stability, retaining 84.16% capacitance after 12,000 cycles. Electrochemical analysis revealed that the charge storage process is predominantly diffusion-controlled with enhanced ion transport kinetics. Furthermore, an asymmetric supercapacitor device assembled using NiCoS-P2 as the positive electrode and activated carbon as the negative electrode demonstrated a wide operating voltage of 1.5 V, delivering an areal capacitance of 0.409 F/cm² (specific capacitance of 204.5 F/g), an energy density of 0.128 mWh/cm², and a power density of 2.99 mW/cm². The device also exhibited excellent long-term stability with 85.3% capacitance retention after 7000 cycles. This work highlights the effectiveness of polymer-assisted structural engineering in optimizing transition metal sulfide electrodes for advanced energy storage applications.: Full article

Nanotechnology has emerged as a key driver in radioisotope batteries, which offer unique advantages for long-term, maintenance-free energy supply in deep space exploration, medical implants, and nuclear waste utilization. This review summarizes recent progress in applying nanomaterials and nanostructures to overcome the limitations of nuclear batteries, including low energy conversion efficiency and poor stability. The main content focuses on the three primary conversion mechanisms of thermoelectric, radio-voltaic, and radio-photovoltaic batteries, discussing high-performance thermoelectric nanomaterials such as SiGe alloys, wide-bandgap semiconductors including diamond and SiC for enhanced carrier collection, and nanoscale radionuclide ources to mitigate self-absorption losses. This review further elaborates on how nanostructure regulation and interface engineering have significantly improved carrier collection efficiency and device stability. These advances have enabled notable civilian applications, such as the BV100 and “Zhulong No.1” nuclear batteries. Despite this progress, challenges remain in ensuring long-term material stability under extreme environments, maintaining performance consistency during macroscopic device integration, and addressing the high fabrication costs. The review concludes by outlining future research directions, including the development of novel nanomaterial systems, innovative nanostructure designs, scalable manufacturing processes, and enhanced device stability and safety, to further advance next-generation radioisotope batteries. Full article

Water electrolysis has emerged as a strategically appealing route for the sustainable production of green hydrogen (H₂) via the hydrogen evolution reaction (HER), though the sluggish kinetics of the oxygen evolution reaction (OER) remains a bottleneck hindering large-scale practical applications. In this regard, an attractive solution is offered by the integration of the ethanol oxidation reaction (EOR) into hybrid water-splitting systems, favorably reducing anodic overpotentials. Nonetheless, an open challenge is related to the fabrication of eco-friendly and economically viable catalysts free from noble metals, combining efficiency and stability. Herein, we explore nickel-oxide-based nanostructures grown onto porous Ni foam scaffolds by a scalable hydrothermal (HT) approach as EOR electrocatalysts. Material properties arising from modulation of the sole HT growth time are investigated by complementary structural, microscopic, and spectroscopic techniques. Electrochemical tests demonstrate good durability and very attractive EOR performances, mainly influenced by the morphology and the NiOOH surface content of the target systems. Overall, the present work advances an attractive route to transition-metal-based electrocatalysts for efficient alcohol-oxidation-assisted water electrolysis. Full article

Biodegradable poly(lactide)/poly(ε-caprolactone) (PLA/PCL) systems functionalized with TiO₂-SiO₂ were synthesized via in situ ring-opening polymerization of a eutectic L-lactide/ε-caprolactone system. This work introduces a TiO₂-SiO₂ composite with a dual function, acting as a catalytic initiator that governs polymerization and microstructure, while simultaneously serving as a reinforcing and photocatalytic phase. The system exhibits high polymerization efficiency, reaching conversions up to 99% with low filler loadings (0.1–1.0 wt%). Structural analyses confirm polymer formation and reveal modifications in ester groups associated with coordination-driven mechanisms. Notably, the presence of TiO₂-SiO₂ promotes increased PLA tacticity, directly influencing mechanical performance. The resulting materials show enhanced tensile strength (~250,000 Pa) and Young’s modulus (1.5–2.0 MPa) compared to conventional systems. In addition, excellent photocatalytic activity was achieved, with up to 99.7% degradation of methyl orange. These findings demonstrate a synergistic strategy to simultaneously control polymer structure and functionality, positioning PLA/PCL–TiO₂-SiO₂ systems as promising multifunctional materials for environmental applications. Full article

The corrosion protection of copper in acidic urban rain environments was studied using self-assembled hydrophobic layers (SAHLs) based on stearic acid (SA), with and without rosehip seed oil (RH). The limited durability of fatty acid-based self-assembled layers under acidic conditions was addressed by correlating surface wettability, morphology, and electrochemical behaviour. Contact angle and SEM analyses showed that SA alone forms a moderately hydrophobic but structurally irregular layer, whereas the addition of 2.0 wt.% RH produces a hierarchical micro/nanostructure with near-superhydrophobic characteristics (CA ≈ 149°). Electrochemical measurements in simulated acid rain solutions (pH 5, 3, and 1) revealed a strong pH dependence of protective performance. While SA-derived layers provided effective protection at pH 5, they deteriorated at lower pH due to protonation of carboxylate anchoring groups and electrolyte ingress. In contrast, SAHLs containing 2.0 wt.% RH maintained polarisation resistance in the MΩ cm² range and inhibition efficiencies above 99% at pH 3, and remained effective even at pH 1. Long-term EIS results indicate a predominantly diffusion-controlled, barrier-type inhibition mechanism associated with defects sealing and interfacial reorganisation. Notably, the rosehip seed oil used is a commercially available, bio-based material with expired shelf life, highlighting the potential of waste-derived resources for sustainable corrosion protection. Full article

Nanophotonics, an interdisciplinary field merging nanotechnology and photonics, has enabled transformative advancements across diverse sectors, including green energy, biomedicine, and optical computing. This review comprehensively examines recent progress in nanophotonic principles and applications, highlighting key innovations in material design, device engineering, and system integration. In renewable energy, nanophotonics allows the use of light-trapping nanostructures and spectral control in perovskite solar cells, concentrating solar power systems, and thermophotovoltaics. This has significantly enhanced solar conversion efficiencies, approaching theoretical limits. In biosensing, nanophotonic platforms achieve unprecedented sensitivity in detecting biomolecules, pathogens, and pollutants, enabling real-time diagnostics and environmental monitoring. Medical applications leverage tailored light–matter interactions for precision photothermal therapy, image-guided surgery, and early disease detection. Furthermore, nanophotonics underpins next-generation optical neural networks and neuromorphic computing, offering ultrafast, energy-efficient alternatives to von Neumann architectures. Despite rapid growth, challenges in scalability, fabrication costs, and material stability persist. Future advancements will rely on novel materials, AI-driven design optimization, and multidisciplinary approaches to enable scalable, low-cost deployment. This review summarizes recent progress and highlights future trends, including novel material systems, multidisciplinary approaches, and enhanced computational capabilities, paving the way for transformative applications in this rapidly evolving field. Full article

Photocatalytic reduction of carbon dioxide (CO₂) into high-value multicarbon products, such as ethylene (C₂H₄), remains a significant challenge due to the difficult C-C coupling process. Potassium poly(heptazine imide) (K-PHI) is a promising photocatalyst, yet efficiently exchanging its interlayer cations to tune catalytic selectivity without causing structural degradation is difficult. Herein, an efficient and green supercritical CO₂ (SC CO₂) assisted ion-exchange strategy was developed to successfully prepare a series of mono-/di-/trivalent cation-doped M-PHI photocatalysts (M = H⁺, Na⁺, Sr⁺, Ca²⁺, Co²⁺, Fe³⁺). Systematic characterizations confirmed that the SC-CO₂ treatment successfully achieved in-depth cation substitution without destroying the intrinsic heptazine framework, effectively regulating the interlayer structure and significantly optimizing the photoelectrochemical charge separation. Among the prepared samples, H-PHI exhibited the optimal photocatalytic CO₂ reduction performance with an outstanding selectivity toward C₂H₄ generation. Under simulated sunlight irradiation for 3 h, the yields of CO, CH₄, and C₂H₄ C₂H₄ C₂H₄ reached 3564.87, 807.32, and 40.00 μmol·g⁻¹, respectively, significantly outperforming pristine K-PHI and other metal-doped samples. Crucially, isotope-tracing experiments utilizing a SC CO₂-DCl treatment detected deuterated CH₄ and C₂H₄ products, providing direct evidence that the hydrogen in the carbon products originates from the introduced protons, thereby elucidating the precise reaction pathway for C-C coupling. This study provides a green and efficient supercritical CO₂ ion exchange strategy for the cation engineering of crystalline carbon nitride, and also offers new ideas and methods for designing high-activity photocatalysts for photocatalytic CO₂ reduction. Full article

In this study, composite silica-containing nanostructures were biosynthesized from residual rice husk through a fermentative process using Aspergillus niger at room temperature without calcination. The obtained nanostructures were initially characterized by UV–Vis spectrophotometry, Fourier-transform infrared spectroscopy (FTIR), and field-emission scanning electron microscopy (FE-SEM) to determine their optical and structural properties compared with chemically synthesized silica. The results demonstrated the successful formation of composite silica-containing amorphous nanostructures under ambient conditions without the use of calcination or mineral acids. UV–Vis analysis revealed intense absorption in the deep ultraviolet region, attributed to electronic transitions associated with Si–O–Si bonds within the amorphous silica network. FTIR analysis enabled the identification of functional groups present on the material surface, providing direct evidence of the nanostructures’ chemical composition. Additionally, FE-SEM micrographs showed that the rice husk surface after biosynthesis exhibited a rough and porous texture with a morphology consistent with the formation of composite silica-containing amorphous nanostructures, in agreement with the characteristic Si–O–Si vibrational bands observed in the FTIR spectra and the strong ultraviolet absorption detected by UV–Vis analysis. Full article