Search Results (2,166)

A multifunctional diagnosis and treatment carrier, ZIF-8@CDs, based on carbon quantum dots (CDs) and the zeolitic imidazolate framework-8 (ZIF-8) metal–organic framework which serves as a core structure for constructing the responsive delivery platform, is developed in this paper. The anticancer drug doxorubicin (DOX) and Survivin oligo (siRNA) are loaded to form a ZIF-8@CDs/DOX@siRNA dual loading platform. CDs of 5–10 nm are synthesized by the solvent method and combined with ZIF-8. Electron microscopy shows that the composites are nearly spherical particles of approximately 200 nm, and the surface potential decreases from +36 mV before loading CDs to +25.7 mV after loading. The composite system shows unique advantages: (1) It has Fenton-like catalytic activity, catalyzes H₂O₂ to generate hydroxyl radicals, and consumes glutathione in the tumor microenvironment. The level of reactive oxygen species (ROS) in the ZIF-8@CDs group is significantly higher than that in the control group. (2) To achieve visual diagnosis and treatment, its fluorescence intensity is superior to that of the traditional Fluorescein isothiocyanate (FITC)-labeled vector; (3) It has a high loading capacity, with the loading amount of small nucleic acids reaching 36.25 μg/mg, and the uptake rate of siRNA by liver cancer cells is relatively ideal. The ZIF-8@CDs/DOX@siRNA dual-loading system is further constructed. Flow cytometry shows that the apoptosis rate of HepG2 cells induced by the ZIF-8@CDs/DOX@siRNA dual-loading system is 49%, which is significantly higher than that of the single-loading system (ZIF-8@CDs/DOX: 34.3%, ZIF-8@CDs@siRNA: 24.2%) and the blank vector (ZIF-8@CDs: 12.6%). The platform provides a new strategy for the integration of tumor diagnosis and treatment through the multi-mechanism synergy of chemical kinetic therapy, gene silencing and chemotherapy. Full article

This study developed a composite binder cold briquetting-direct reduction process for zinc removal and resource recovery from zinc-containing dust. Through systematic briquetting and reduction experiments, the optimal briquette parameters were identified, and the mechanisms of zinc migration and removal during reduction were discussed. The results showed that under optimized reduction conditions at 1275 °C for 25 min and with 4% carbon content in the briquettes, the process achieved a zinc removal rate of 98.25% and an iron metallization rate of 90.54%, indicating high Zn removal performance under the tested conditions. Notably, compared with briquettes prepared with conventional organic binders (OB1), the composite binder (CB1) briquettes exhibited higher compressive strength while maintaining comparable Zn removal and metallization performance. The CB1 offers both economic advantages and improved mechanical strength, being successfully applied in industrial lines. Moreover, this process offers an industrially applicable route for the efficient treatment and resource utilization of zinc-bearing dust in the steel industry. Full article

Zinc (Zn) in excess is very toxic for plants and can limit agriculture. Carbon-based engineered nanomaterials with high electron mobility and electron-accepting capability may be essential for mitigating heavy metal stress. In the present study, the protective role of some fullerene C₆₀ derivatives (fullerenol [C₆₀(OH)_22–24] and the arginine C₆₀ [C₆₀(C₆H₁₃N₄O₂)₈H₈]) were tested for the first time against Zn toxicity in Cucumis sativus L. (cucumber). Plants were grown hydroponically at three concentrations of fullerenes (0, 2, and 10 mg L⁻¹) without or with 40 µM Zn for 17 days. Plant growth, leaf chlorosis, and nutritional imbalances in combination with a metabolomics approach were analyzed. The Zn-treated plants show chlorotic leaves, the retarded growth of shoots (−20%), and roots (−49%) and nutrient imbalance. Addition of fullerene C₆₀ derivatives suppressed loss in the dry biomass of leaves (15%) and roots (40%; fullerenol only) induced by high Zn. However, they did not alter leaf chlorophyll, shoot dry biomass, and elemental composition, including leaf Zn. Moreover, the Zn of xylem sup from roots remained unchanged by fullerenes. In an adsorption experiment, the amounts of Zn adsorbed by tested C₆₀ were below the detection limits. The addition of C₆₀ derivatives slightly changed the metabolite profiling in stressed plants. Nevertheless, in fullerene-treated plants, the abundance of some Zn-responsible metabolites tended to be altered in the opposite direction as compared with the metabolic responses to excessive Zn alone. There were several up-regulated metabolites protecting plants under oxidative stress. We speculate that fullerene C₆₀ derivatives have the ability to increase antioxidant non-enzyme activity at least, improving some growth parameters. However, fullerenes did not reduce Zn transport from the root to the shoots. We concluded that the low capacity of these compounds to buffer Zn in the root zone might limit the efficiency of fullerene derivatives against Zn toxicity. Our results provide new evidence for the crucial role of Zn–fullerene interactions in the amelioration of Zn toxicity in plants. Full article

The effect of CO₂ laser treatment on the surface composition and properties of a woven fabric (polyester (PET) fiber (59 wt%)/cotton (CO) fiber (31 wt%)/stainless-steel (SS) metal fibers (10 wt%)) was investigated across a range of laser intensities (19.1 × 10⁶ to 615.0 × 10⁶ W/m²). Elemental analysis using wavelength-dispersive X-ray fluorescence (WD-XRF) revealed that for an intensity up to 225.4 × 10⁶ W/m², the carbon content on the fabric surface increased while the oxygen content decreased, indicating thermally induced surface modification. Fourier transform infrared (FT-IR) spectroscopy confirmed that no new chemical bonds were formed, suggesting that the changes observed were predominantly physical in nature. High-resolution scanning electron microscopy (HR-SEM) showed progressive fiber fusion and surface smoothing with increasing laser intensity, consistent with polyester melting. Tensile testing demonstrated a significant decline in peak load and elongation at peak load with rising laser fluence, indicating mechanical embrittlement. Overall, CO₂ laser treatment alters the morphology and elemental composition of the fabric surface without inducing major chemical decomposition, markedly reducing its mechanical strength. Full article

Herein, we propose a simple and cost-effective method for fabricating moderate-sensitivity surface-enhanced Raman scattering (SERS) substrates using Cu-plasma polymer fluorocarbon (Cu-PPFC) nanocomposite films fabricated through RF sputtering. The use of a composite target composed of carbon nanotube (CNT), Cu, and polytetrafluoroethylene (PTFE) powders (5:60–80:35–15 wt%) offers the advantage of the simple fabrication of moderate-sensitivity SERS substrates with a single cathode compared to co-sputtering. X-ray photoelectron spectroscopy (XPS) revealed that the film surface was partially composed of metallic Cu with Cu-F bonds and Cu–O bonds, confirming the coexistence of the conducting and plasmon-active domains. UV-VIS spectroscopy revealed a distinct absorption peak at approximately 680 nm, indicating the excitation of localized surface plasmon resonances in the Cu nanoclusters embedded in the plasma polymer fluorocarbon (PPFC) matrix. Atomic force microscopy and grazing incidence small-angle X-ray scattering analyses confirmed that the Cu nanoparticles were uniformly distributed with interparticle distances of 20–35 nm. The Cu-PPFC nanocomposite film with the highest Cu content (80 wt%) exhibited a Raman enhancement factor of 2.18 × 10⁴ for rhodamine 6G, demonstrating its potential as a moderate-sensitivity SERS substrate. Finite-difference time-domain (FDTD) simulations confirmed the strong electromagnetic field localization at the Cu-Cu nanogaps separated by the PPFC matrix, corroborating the experimentally observed SERS enhancement. These results suggest that a Cu-PPFC nanocomposite film, easily fabricated using a composite target, provides an efficient and scalable route for fabricating reproducible, inexpensive, and moderate-sensitivity SERS substrates suitable for practical sensing applications. Full article

The field of electrochemical devices, encompassing energy storage, fuel cells, electrolysis, and sensing, is fundamentally reliant on the electrode materials that govern their performance, efficiency, and sustainability. Traditional materials, while foundational, often face limitations such as restricted reaction kinetics, structural deterioration, and dependence on costly or scarce elements, driving the need for continuous innovation. Emerging electrode materials are designed to overcome these challenges by delivering enhanced reaction activity, superior mechanical robustness, accelerated ion diffusion kinetics, and improved economic feasibility. In energy storage, for example, the shift from conventional graphite in lithium-ion batteries has led to the exploration of silicon-based anodes, offering a theoretical capacity more than tenfold higher despite the challenge of massive volume expansion, which is being mitigated through nanostructuring and carbon composites. Simultaneously, the rise of sodium-ion batteries, appealing due to sodium’s abundance, necessitates materials like hard carbon for the anode, as sodium’s larger ionic radius prevents efficient intercalation into graphite. In electrocatalysis, the high cost of platinum in fuel cells is being addressed by developing Platinum-Group-Metal-free (PGM-free) catalysts like metal–nitrogen–carbon (M-N-C) materials for the oxygen reduction reaction (ORR). Similarly, for the oxygen evolution reaction (OER) in water electrolysis, cost-effective alternatives such as nickel–iron hydroxides are replacing iridium and ruthenium oxides in alkaline environments. Furthermore, advancements in materials architecture, such as MXenes—two-dimensional transition metal carbides with metallic conductivity and high volumetric capacitance—and Single-Atom Catalysts (SACs)—which maximize metal utilization—are paving the way for significantly improved supercapacitor and catalytic performance. While significant progress has been made, challenges related to fundamental understanding, long-term stability, and the scalability of lab-based synthesis methods remain paramount for widespread commercial deployment. The future trajectory involves rational design leveraging advanced characterization, computational modeling, and machine learning to achieve holistic, system-level optimization for sustainable, next-generation electrochemical devices. Full article

Carbon–metal composite NiCrFeC coatings, prepared with and without controlled oxygen addition, were investigated to evaluate the influence of oxygen on the structure, mechanical response, and tribological performance. X-ray diffraction revealed that oxygen-containing films (NiCrFeC + O₂) exhibit a mixed metallic–oxide microstructure with CrNi, CrO, and NiO phases, whereas oxygen-free coatings show only CrNi crystalline peaks. The incorporation of oxygen led to a substantial increase in nano-hardness, from 0.84 GPa for NiCrFeC to 1.59 GPa for NiCrFeC + O₂. Scratch testing up to 100 N indicated improved adhesion and higher critical loads for the oxygen-rich coatings. Tribological measurements performed under dry sliding conditions using a sapphire ball showed a significant reduction in friction: NiCrFeC + O₂ stabilized at ~0.20, while NiCrFeC exhibited values between 0.25 and 0.35 at 0.5 N and 0.4–0.5 at 1 N, accompanied by non-uniform sliding due to coating failure. Wear-track analysis confirmed shallower penetration depths and narrower wear scars for NiCrFeC + O₂, despite similar initial roughness (~35 nm). These findings demonstrate that oxygen incorporation enhances hardness, adhesion, and wear resistance while substantially lowering friction, making NiCrFeC + O₂ coatings promising for low-friction dry-sliding applications. Full article

Zeolite imidazolate frameworks (ZIFs)-derived carbon materials have garnered widespread attention as peroxymonosulfate (PMS) activators in removing antibiotics because of their excellent catalytic performance. However, most carbon materials derived from ZIFs exhibit limited efficacy in treating high-concentration (>10 ppm) antibiotic wastewater, and their synthesis methods are environmentally unfriendly. Herein, we develop a simple and environmentally friendly preparation method to synthesize a new type of nitrogen-doped carbon-supported carbon nanotubes coated with cobalt nanoparticle (Co-CNTs@NC) composites via high-temperature calcination of cobalt–zinc bimetallic ZIFs. The material characterization results confirm the successful preparation of Co-CNTs@NC composites featuring a high specific surface area (512.13 m²/g) and a Co content of 5.38 wt%. Across an initial pH range of 3.24–9.00, the Co-CNTs@NC/PMS catalytic system achieved over 84.17% degradation of 20 mg/L tetracycline hydrochloride within 90 min, demonstrating its favorable pH tolerance. The singlet oxygen-dominated degradation mechanism was confirmed by quenching experiments and electron paramagnetic resonance characterization. This work can provide technical guidance and reference significance for the preparation of metal–carbon materials derived from ZIFs with excellent efficiency of removal of high-concentration antibiotics. Full article

Nanoparticle-mediated photothermal conversion exploits the unique light-to-heat transduction properties of engineered nanomaterials to address challenges in energy, water, and healthcare. This review first examines fundamental mechanisms—localized surface plasmon resonance (LSPR) in plasmonic metals and broadband interband transitions in semiconductors—demonstrating how tailored nanoparticle compositions can achieve >96% absorption across 250–2500 nm and photothermal efficiencies exceeding 98% under one-sun illumination (1000 W·m⁻², AM 1.5G). Next, we highlight advances in solar steam generation and desalination: floating photothermal receivers on carbonized wood or hydrogels reach >95% efficiency in solar-to-vapor conversion and >2 kg·m⁻²·h⁻¹ evaporation rates; three-dimensional architectures recapture diffuse flux and ambient heat; and full-spectrum nanofluids (LaB₆, Au colloids) extend photothermal harvesting into portable, scalable designs. We then survey photothermal-enhanced thermal energy storage: metal-oxide–paraffin composites, core–shell phase-change material (PCM) nanocapsules, and MXene– polyethylene glycol—PEG—aerogels deliver >85% solar charging efficiencies, reduce supercooling, and improve thermal conductivity. In biomedicine, gold nanoshells, nanorods, and transition-metal dichalcogenide (TMDC) nanosheets enable deep-tissue photothermal therapy (PTT) with imaging guidance, achieving >94% tumor ablation in preclinical and pilot clinical studies. Multifunctional constructs combine PTT with chemotherapy, immunotherapy, or gene regulation, yielding synergistic tumor eradication and durable immune responses. Finally, we explore emerging opto-thermal nanobiosystems—light-triggered gene silencing in microalgae and poly(N-isopropylacrylamide) (PNIPAM)–gold nanoparticle (AuNP) membranes for microfluidic photothermal filtration and control—demonstrating how nanoscale heating enables remote, reversible biological and fluidic functions. We conclude by discussing challenges in scalable nanoparticle synthesis, stability, and integration, and outline future directions: multicomponent high-entropy alloys, modular photothermal–PCM devices, and opto-thermal control in synthetic biology. These interdisciplinary innovations promise sustainable solutions for global energy, water, and healthcare demands. Full article

Although carbon filters (CF) can exhibit limited adsorption/selectivity for certain emerging pollutants and operating conditions, incorporating carbon–metal-oxide composites provides a platform to study how surface chemistry, charge distribution and oxide dispersion influence adsorption behavior. This study investigates the incorporation of metal oxides (Fe₃O₄, TiO₂ and CaO) into a commercial carbon filter via mechanical milling, focusing on fundamental changes in surface properties and methylene blue (MB) adsorption mechanisms. The synthesized oxides were characterized by X-ray diffraction and scanning electron microscopy, confirming crystalline structures with crystalline sizes between 11 and 23 nm. Composite filters with varying oxide contents (10–30 wt%) were evaluated for point of zero charge (PZC), surface charge distribution and methylene blue (MB) adsorption. The kinetic experiments were adjusted to pseudo-second order (PSO). Although the maximum adsorption capacity (2.75 mg·g⁻¹ for CaO-modified filters) is lower than commercially activated carbons, this work clarifies how oxide type and dispersion control adsorption performance and interaction mechanisms. Langmuir and Freundlich models revealed monolayer adsorption with favorable dye-surface interactions. These models provide key insights into the role of oxide type and pH in the dye removal process. Full article

Nitrogen dioxide (NO₂) is a major atmospheric pollutant and also a recoverable nitrogen resource, for which adsorption offers a promising technical pathway. This review systematically summarizes the recent progress in the removal of NO₂ from flue gas by adsorption methods, with a focus on material-level and process-level advancements. From the material perspective, three representative adsorbents—zeolites, activated carbons, and metal oxides—are comparatively evaluated in terms of their physicochemical properties, active sites, and adsorption mechanisms. Emphasis is placed on their adsorption capacity, selectivity, and hydrothermal stability, supported by both experimental and theoretical insights. From the process perspective, four adsorption-based technologies—Pressure Swing Adsorption (PSA), Temperature Swing Adsorption (TSA), Vacuum Pressure Swing Adsorption (VPSA), and Vacuum Temperature Swing Adsorption using multiple Gas circulations (GVTSA)—are analyzed regarding their principles, operational workflows, and engineering applications, with particular attention to the process intensification potential of GVTSA. The review identifies existing challenges in terms of material stability under complex conditions and process scalability, especially for severe environments such as nuclear reprocessing tail gases. Finally, future research directions are proposed toward developing multifunctional composite adsorbents with high capacity, strong environmental tolerance, and excellent regenerability, along with optimized and integrated adsorption processes, to achieve efficient NO₂ abatement and high-value recovery. Full article

Extreme environments such as low pressure, high temperature, and intense radiation pose severe challenges for humidity sensors, causing conventional hygroscopic materials to exhibit sluggish responses, drift, and instability. In response, recent research has adopted multi-level strategies involving material modification, structural engineering, and packaging optimization to enhance the adaptability of humidity-sensitive materials in extreme environments. This review examines humidity sensing from an environmental perspective, integrating sensing mechanisms, material classifications, and application scenarios. The performance, advantages, and limitations of six major categories of humidity-sensitive materials, including carbon-based, metal oxides, conductive and insulating polymers, two-dimensional (2D) materials, and composites, are systematically summarized under extreme conditions. Finally, emerging development trends are discussed, highlighting a shift from material-driven to system-driven approaches. Future progress will rely on multidisciplinary integration, including interface engineering, multiscale structural design, and intelligent algorithms, to achieve higher accuracy, stability, and durability in extreme-environment humidity sensing. Full article

The development of efficient and stable oxygen evolution reaction (OER) electrocatalysts based on non-precious metals is pivotal for advancing sustainable energy conversion technologies. We present a facile and green strategy for synthesizing a high-performance HO-CDs-FeOOH/NF(D) composite catalyst by leveraging a synergistic system of FeCl₃/urea deep eutectic solvent (DES) and hydroxyl-functionalized carbon dots (HO-CDs). This system orchestrates the rapid, in situ growth of FeOOH on nickel foam (NF) via simple immersion, wherein the DES acts as both an etchant and an iron source, while the HO-CDs induce a morphological transformation from sheet-like to granular stacking, thereby constructing highly active interfaces and increasing the density of accessible catalytic sites. The optimized catalyst exhibits exceptional OER performance, requiring an overpotential of only 251 mV to achieve 50 mA cm⁻², with a Tafel slope of 55.4 mV dec⁻¹. Moreover, it demonstrates outstanding stability, maintaining 98% of its initial current density after 24 h of continuous operation and showing negligible performance decay after 3000 cycles. This work presents a straightforward approach for designing high-performance Fe-based electrocatalysts through carbon dot-mediated morphology control via a facile DES-based impregnation strategy. Full article

To obtain an excellent electromagnetic wave (EMW) absorption material, a strategy was proposed in this study with the aid of in-situ growth of carbon nanotubes (CNTs) on the surface of a metal–organic framework (MOF)-derived FeCoNiMnMg high-entropy alloy (HEA). The HEA@CNT composite was successfully prepared via a solvothermal method combined with a one-step pyrolysis process. With the pyrolysis temperature increasing from 600 °C to 800 °C, the length of CNTs grew from 200 nm to about 600 nm approximately, while the defect density of CNTs was enhanced. This structural evolution significantly improved the dielectric properties and impedance matching. Consequently, the sample prepared at 800 °C (HEA@CNT-800) exhibited outstanding microwave absorption performances, achieving a minimum reflection loss (RL_min) of −57.52 dB at a matched thickness of 2.3 mm and an effective absorption bandwidth (EAB) of 4.4 GHz at a thinner thickness of 1.9 mm. This work provides a novel perspective for designing high-performance MOF-derived absorption materials. Full article

Metal-composite joints, leveraging the high specific strength/stiffness and superior fatigue resistance of carbon fiber reinforced polymers (CFRP) alongside metallic materials’ excellent toughness and formability, have become prevalent in aerospace structures. Fastener flexibility serves as a critical parameter governing load distribution prediction and fatigue life assessment, where accurate quantification directly impacts structural reliability. Current approaches face limitations: experimental methods require extended testing cycles, numerical simulations exhibit computational inefficiency, and conventional machine learning (ML) models suffer from “black-box” characteristics that obscure mechanical principle alignment, hindering aerospace implementation. This study proposes an integrated framework combining numerical simulation with explainable ML for fastener flexibility analysis. Initially, finite element modeling (FEM) constructs a dataset encompassing geometric features, material properties, and flexibility values. Subsequently, a random forest (RF) prediction model is developed with five-fold cross-validation and residual analysis ensuring accuracy. SHapley Additive exPlanations (SHAP) methodology then quantifies input features’ marginal contributions to flexibility predictions, with results interpreted in conjunction with theoretical flexibility formulas to elucidate key parameter influence mechanisms. The approach achieves 0.99 R2 accuracy and 0.11 s computation time while resolving explainability challenges, identifying fastener diameter-to-plate thickness ratio as the dominant driver with negligible temperature/preload effects, thereby providing a validated efficient solution for aerospace joint optimization. Full article