Search Results (67)

The peripheries of rare-metal metallogenic systems frequently host skarn-type or hydrothermal vein-type Pb-Zn deposits, though their genetic connections with parental systems remain debated. The newly identified Gariatong W-Mo polymetallic metallogenic system in the Lhasa Terrane displays well-defined Nb-Ta-Rb, Mo-W, W-Mo, W-Bi, and Pb-Zn-Ag metallogenic zoning, establishing it as an exemplary site for investigating genetic relationships between Pb-Zn and rare-metal mineralization. This investigation targets skarn-type Pb-Zn deposits spatially associated with rare-metal orebodies at Gariatong, utilizing integrated analytical approaches, including in situ LA-ICP-MS trace-element analysis of sulfides, sulfur isotope geochemistry, and LA-ICP-MS elemental mapping of sphalerite, to constrain metal sources, characterize fluid evolution, and establish genetic correlations with the rare-metal system. Key findings include the following: (1) sphalerite shows enrichment in Fe, Mn, Co, and Cd, while pyrite contains elevated As, Pb, Co, Cu, and Mn. Fe, Cd, and Mn primarily occur as solid solutions or nanoparticles, whereas As and Pb exist as micro-inclusions. (2) Sphalerite Zn/Cd ratios (73.6–184) and Co-Ni-As ternary diagrams confirm a magmatic–hydrothermal skarn origin. (3) Mineralization occurred under moderate-temperature, mildly oxidized conditions, as constrained by sphalerite Fe contents and mineral assemblages. Sulfur isotope compositions (δ³⁴S = −1.0‰ to 3.2‰; mean: 1.9‰) indicate a magmatic sulfur source. This study reveals that the Nb-Ta-Rb mineralization, quartz-vein- and greisen-type W-Mo deposits, and skarn-type Pb-Zn orebodies—all genetically associated with highly fractionated granites—constitute an integrated magmatic–hydrothermal system with vertical (depth-related) zoning relative to the granitic intrusion. These results provide critical constraints for understanding rare-metal–Pb-Zn genetic associations and suggest that Pb-Zn mineralization may serve as a key exploration indicator for rare metals in the Lhasa Terrane. Full article

Background: Minimally invasive hyperthermia and regenerative therapies require materials that deliver precise, localized heat without compromising biocompatibility. Most conventional polymers are thermally insulating and challenging to control in vivo, motivating this review. Objectives: We aimed to (i) examine the use of thermally enhanced biopolymers in hyperthermia-based therapies, (ii) appraise evidence from clinical and preclinical studies, (iii) identify and classify principal applications in regenerative medicine. Methods: A PRISMA-guided systematic review (2020–2025) with predefined inclusion/exclusion criteria was conducted and complemented by a bibliometric analysis using VOSviewer for mapping and visualization. Results: Modifying biopolymers—via functionalization with photothermal or magnetic nanoagents (Au; Fe₂O₃/Fe₃O₄/CoFe₂O₄; CuS; Ag; MXenes, e.g., Nb₂C), crosslinking strategies, and hybrid formulations—significantly increased thermal conductivity, enabling localized hyperthermia and controlled drug release. In vitro and in vivo studies showed that europium-doped iron oxide nanoparticles embedded in chitosan generated heat efficiently while sparing healthy tissues, underscoring the need to balance biocompatibility and thermal performance. Hydrogel systems enriched with carbon nanomaterials (graphene, carbon nanotubes) and matrices such as GelMA, PNIPAM, hyaluronic acid, and PLA/PLGA demonstrated tissue compatibility and effective thermal behavior; graphene was compatible with neural tissue without inducing inflammation. Conclusions: Thermally conductive biopolymers show growing potential for oncology and regenerative medicine. The evidence supports further academic and interdisciplinary research to optimize safety, performance, and translational pathways. Full article

Reactive co-sputtering was applied to deposit TaN-(Ag,Cu) nanocomposite films on Si and tool steels. Prior to post-deposition annealing, the films were deposited with TaN cap (diffusion barrier) layers in various thicknesses in order to slow down the nucleation and growth of emerging Ag and Cu particles. The thickness of the cap layers was set at 5, 10, 20, or 50 nm. The films were then annealed using Rapid Thermal Annealing (RTA) at 400 °C to induce the nucleation and growth of Ag and Cu nanoparticles. These films’ surface morphologies and structures were examined. The samples were tested for their anti-wear and antibacterial behaviors against Gram-positive S. aureus and Gram-negative E. coli, with a variation in cap layer thickness. It is found that, through the application of TaN cap layers, the out-diffusion of Ag and Cu atoms may be slowed down. The surface concentrations of Ag and Cu might decrease from 35 at.% and 17 at.% to 18 at.% and 6 at.%, respectively, when the cap layer thickness increases to 50 nm (after being annealed for 12 min). The diffusion mechanism is proposed to explain the formation of nanoparticles on the surface through boundary diffusion. Antibacterial behaviors against both bacteria, as well as tribological properties, could still be effective but become less significant with an increase in the cap layer thickness. The antibacterial efficiency after 3 h testing decreased from 99% to 5% and 8% against E. coli and S. aureus, respectively. At 12 h, all the samples reached >99% antibacterial efficiency, despite the variation in cap thickness. For sliding wear, the wear rate was doubled when the cap thickness increased to 50 nm (when the normal load was 1 N). On the other hand, the difference was minor when the normal load was changed to 5 N. The sliding lifetime of the samples was studied using a tribometer. The total lifetime may increase with an increase in the cap thickness. The wear is found to be due to the oxidation of Ag and Cu nanoparticles, which results in the loss of low coefficient behaviors. Full article

As the global energy industry shifts away from fossil fuels, there is a growing need for sustainable and renewable hydrogen production methods. This research investigates the potential of using biochar derived from animal waste as a precursor for creating effective catalysts for the hydrogen evolution reaction (HER). By incorporating copper and nickel into the biochar through hydrothermal processing, the study examined the resulting catalysts’ structural, chemical, and catalytic properties. Techniques such as scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and Fourier transform infrared spectroscopy (FTIR) confirmed the successful integration of metallic nanoparticles and revealed notable changes in surface morphology, elemental composition, and functional group distribution. The Cu–Ni co-doped biochar catalyst (Cu–Ni/BC) demonstrated a significant 45% increase in hydrogen evolution efficiency compared to the undoped biochar control sample. These results highlight the synergistic effects of copper and nickel in enhancing the catalyst’s electron transfer capabilities and active site availability. This study offers a sustainable, cost-effective, and environmentally friendly alternative to conventional hydrogen production catalysts, presenting considerable potential for waste valorization while promoting clean energy solutions. The research aligns with circular economy principles, contributing to the advancement of sustainable energy technologies. Full article

Tomatoes are a fundamental part of the daily diet, rich in carbohydrates, vitamins, minerals, carotenoids, and polyphenols. Nonetheless, optimal fruit yield and quality typically depend on the application of synthetic agrochemicals. However, the irrational use of these agrochemicals has caused various environmental problems. Therefore, it is necessary to develop alternatives to conventional agrochemical products. Applying nanomaterials as fertilizers in tomato production is emerging as a promising approach, with documented improvements in germination, vegetative development, and fruit yield. Therefore, we present a comprehensive review of recent developments (2015–2024) in the application of nanomaterials in tomato crops, with a particular emphasis on the significance of nanomaterial characteristics in their role as fertilizers. Several types of nanomaterials, such as ZnO, Ag, TiO₂, Si, hydroxyapatite, P, Zn, Se, CuO, Cu, Fe, Fe₂O₃, CaO, CaCO₃, and S, have been evaluated as fertilizers for tomato crops, with ZnO nanoparticles being the most extensively studied. However, it is pertinent to conduct further research on the less-explored nanomaterials to gain a deeper understanding of their effects on seed germination, plant growth, and fruit quality and quantity. Full article

Cobalt-based perovskite oxides exhibit remarkable catalytic activity owing to abundant oxygen vacancies and mixed ionic–electronic conductivity, but they suffer from structural instability. In contrast, iron-based perovskite oxides are thermochemically stable under oxidizing and reducing conditions but are catalytically limited. To combine these complementary properties, a composite perovskite oxide was designed and prepared by infiltrating Sr_0.95Ce_0.05CoO_3−δ (SCC) into Ba_0.5Sr_0.5Fe_0.8Cu_0.2O_3−δ (BSFC). The SCC precursor solution was dropwise applied to a BSFC|SDC|BSFC symmetric cell and heat treated. Surface morphology and compositional analyses confirmed the distribution of SCC nanoparticles on the BSFC surface. High-temperature X-ray diffraction and Rietveld refinement results revealed that both BSFC and SCC retained the cubic perovskite structure (space group Pm-3m) at room temperature. No phase transition or secondary phase formation was observed during heating from 200 to 800 °C, and the peak shifts are attributed to thermal expansion and possible oxygen loss at elevated temperatures. Upon cooling, the diffraction patterns returned to their initial state, confirming a high-temperature structural stability. XPS analysis showed an increase in the satellite peak intensity associated with Fe³⁺ after SCC infiltration, and the average oxidation state of Fe decreased from 3.52 (BSFC) to 3.49 (composite perovskite oxide). The O 1s spectra revealed a higher relative content of surface-adsorbed oxygen species in the composite, indicating increased oxygen vacancy formation. Full article

Cu-based layered double hydroxides (LDH) have been extensively employed as catalyst precursors. However, due to the Jahn–Teller effect of copper ions, it is a challenge to synthesize well-crystallized LDH with a high Cu content, which usually contains considerable CuO impurity. By adding competitive ligands during the coprecipitation process, such as glycine, a well-crystallized Cu-rich LDH with less CuO impurity was successfully synthesized. The Cu-Mg-Al mixed oxides derived from the well-crystallized Cu-rich LDH have relatively high S_BET, large pore volume, and well dispersion of Cu nanoparticles. The derived catalyst exhibited unexpectedly high catalytic activity in the water–gas shift (WGS) reaction, and the mass-specific reaction rate was reached as high as 33.5 μmol_CO${·\mathrm{g}}_{\mathrm{cat}}^{-1}$·s⁻¹ at 200 °C. The high catalytic activity of this catalyst may originate from the high S_BET and well dispersion of Cu particles and metal oxides. Moreover, the derived catalyst also displayed outstanding long-term stability in the WGS reaction, which should benefit from the enhanced metal–support interaction. Full article

This study evaluates the wear and corrosion resistance of the Cu-50Ni-5Al alloy reinforced with CeO₂ nanoparticles for potential use as anodes in molten carbonate fuel cells (MCFCs). Cu–50Ni–5Al alloys were synthesized, with and without the incorporation of 1% CeO₂ nanoparticles, by the mechanical alloying method and spark plasma sintering (SPS). The samples were evaluated using a single scratch test with a cone-spherical diamond indenter under progressive normal loading conditions. A non-contact 3D surface profiler characterized the scratched surfaces to support the analysis. Progressive loading tests indicated a reduction of up to 50% in COF with 1% NPs, with specific values drop-ping from 0.48 in the unreinforced alloy to 0.25 in the CeO₂-doped composite at 15 N of applied load. Furthermore, the introduction of CeO₂ decreased scratch depths by 25%, indicating enhanced wear resistance. The electrochemical behavior of the samples was evaluated by electrochemical impedance spectroscopy (EIS) in a molten carbonate medium under a H₂/N₂ atmosphere at 550 °C for 120 h. Subsequently, the corrosion products were characterized using X-ray diffraction (XRD), scanning electron microscopy coupled with energy dispersive spectroscopy (SEM-EDS), and X-ray photoelectron spectroscopy (XPS). The results demonstrated that the CeO₂-reinforced alloy exhibits superior electro-chemical stability in molten carbonate environments (Li₂CO₃-K₂CO₃) under an H₂/N₂ atmosphere at 550 °C for 120 h. A marked reduction in polarization resistance and a pronounced re-passivation effect were observed, suggesting enhanced anodic protection. This effect is attributed to the formation of aluminum and copper oxides in both compositions, together with the appearance of NiO as the predominant phase in the materials reinforced with nanoparticles in a hydrogen-reducing atmosphere. The addition of CeO₂ nanoparticles significantly improves wear resistance and corrosion performance. Recognizing this effect is vital for creating strategies to enhance the material’s durability in challenging environments like MCFC. Full article

This study examines the impact of Au nanoparticles (Au-NPs) on the chemoresistive gas sensing properties as a function of particle size. The sensing material is composed of ultrathin CuO/Cu₂O films, which are fabricated by either thermal deposition technology or spray pyrolysis. These are used on a silicon nitride (Si₃N₄) micro hotplate (µh) chip with Pt electrodes and heaters. The gas sensing material is then functionalised with Au-NP of varying sizes (12, 20, and 40 nm, checked by transmission electron microscopy) using drop coating technology. The finalised sensors are tested by measuring the electrical resistance against various target gases, including carbon monoxide (CO), carbon dioxide (CO₂), and a mixture of hydrocarbons (HC_Mix), in order to evaluate any cross-sensitivity issues. While the sensor response is markedly contingent on the structural surface, our findings indicate that the dimensions of the Au-NPs exert a discernible influence on the sensor’s behaviour in response to varying target gases. The 50 nm thermally evaporated CuO/Cu₂O layers exhibited the highest sensor response of 78% against 2000 ppm CO₂. In order to gain further insight into the surface of the sensors, a scanning electron microscope (SEM) was employed, and to gain information about the composition, Raman spectroscopy was also utilised. Full article

Copper nanoparticles have been integrated onto the framework of modified NH₂–MIL–125(Ti), a metal–organic framework (MOF), and evaluated as catalysts for converting CO₂ into valuable products. The modified MOF was achieved through a post-synthetic modification process involving the partial replacement of titanium with zirconium or cerium within the MOF’s structure. The objective behind this alteration is to create a synergistic effect between the MOF, serving as a support matrix, and the embedded copper nanoparticles, thereby enhancing the performance of the catalyst. The obtained catalysts were characterized and evaluated in the hydrogenation of CO₂ to methanol under different experimental conditions, reaching CO₂ conversions of up to 5%, with a selectivity towards methanol that reached values of up to 60%. According to the obtained results, the catalyst composed of Ti, Zr and Cu stood out for having the highest CO₂ conversion and selectivity towards methanol, in addition to practically inhibiting the production of methane. These results demonstrate that the interaction of the framework with the Cu nanoparticles, and thus its catalytic properties, can be changed by modifying the properties of the MOF. Full article

Copper oxide nanoparticles (CuO-NPs) induce neurological diseases, including neurobehavioral defects and neurodegenerative diseases. Direct evidence indicates that CuO-NPs induce inflammation in the central nervous system and cause severe neurotoxicity. However, the mechanism of CuO-NP-induced damage to the nervous system has rarely been studied, and the toxicity of different CuO-NP particle sizes and their copper ion (Cu²⁺) precipitation in microglia (BV2 cells) is worth exploring. Therefore, this study investigated CuO-NPs with different particle sizes (small particle size: S-CuO-NPs; large particle size: L-CuO-NPs), Cu²⁺ with equal molar mass (replaced by CuCl₂ [Equ group]), and Cu²⁺ precipitated in a cell culture solution with CuO-NPs (replaced by CuCl₂ [Pre group]), and examined the mechanism of action of each on BV2 microglia after co-culture for 12 h and 24 h. The activity of BV2 cells decreased, the morphology was damaged, and the apoptosis rate increased in all the exposed groups. Toxicity increased time- and dose-dependently, and was highest in the Equ group, followed by the S-CuO-NPs, L-CuO-NPs, and Pre groups, respectively. Subsequently, we investigated the mechanism of S-CuO-NP-induced cell injury, and revealed that S-CuO-NPs induced oxidative stress and inflammatory response and increased the membrane permeability of BV2 cells. Moreover, S-CuO-NPs reduced the ratio of p-CSF-1R/CSF-1R, p-PLCγ2/PLCγ2, p-extracellular signal-regulated kinase (ERK)/ERK, p-Nrf2/Nrf2, and Bcl-2/Bax protein expression in microglia, and elevated cleaved caspase-3 expression. The CSF-1R/PLCγ2/ERK/Nrf2 apoptotic pathway was activated. The downregulation of CX3CR1, CSF-1R, brain-derived neurotrophic factor (BDNF), and IGF-1 protein expression indicates impairment of the repair and protection functions of microglia in the nervous system. In summary, our results reveal that CuO-NPs promote an increase in inflammatory molecules in BV2 microglia through oxidative stress, activate the CSF-1R/PLCγ2/ERK/Nrf2 pathway, cause apoptosis, and ultimately result in neurofunctional damage to microglia. Full article

Large-scale superconductor applications necessitate a superconducting matrix with pinning sites (PSs) that immobilize vortices at elevated temperatures and magnetic fields. While previous works focused on the single addition of nanoparticles, the simultaneous inclusion of different nanoparticles into a superconducting matrix can be an effective way to achieve an improved flux pinning capacity. The purpose of this study is to explore the influence of mixed-nanoparticle pinning, with the co-addition of non-magnetic (BaTiO₃; BT) and various types of magnetic spinel ferrite (MFe₂O₄, abbreviated as MFO, where M = Mn, Co, Cu, Zn, and Ni) nanoparticles, on the superconductivity and flux pinning performances of the high-temperature superconductor YBa₂Cu₃O_y (YBCO). An analysis of X-Ray diffraction (XRD) data of BT–MFe₂O₄-co-added YBCO samples showed the formation of an orthorhombic structure with Pmmm symmetry. According to electrical resistivity measurements, the emergence of the superconducting state below $T_c^{offset}$ (zero-resistivity temperature) was proven for all samples. The highest $T_c^{offset}$ value was recorded for the Y-BT-MnFO sample, while the minimum value was obtained for the Y-BT-ZnFO sample. Direct current (DC) magnetization results showed good magnetic flux pinning performance for all the co-added samples compared to the pristine sample but with some discrepancies. At 77 K, the values of the self-critical current density (self-$J_{cm}$) and maximum pinning force ($F_{pmax}$) for the Y-BT-MnFO sample were found to be eight times higher and seventeen times greater than those for the pristine sample, respectively. The results acquired suggested that mixing the BT phase with an appropriate type of spinel ferrite nanoparticles can be a practical solution to the problem of degradation of the critical current density of the YBCO material. Full article

Self-doped CuS nanoparticles (NPs) were successfully synthesized via microwave-assisted polyol process to act as co-catalysts to TiO₂ nanofiber (NF)-based photoanodes to achieve higher photocurrents on visible light-assisted water electrolysis. The strategy adopted to perform the copper cation sulfidation in polyol allowed us to overcome the challenges associated with the copper cation reactivity and particle size control. The impregnation of the CuS NPs on TiO₂ NFs synthesized via hydrothermal corrosion of a metallic Ti support resulted in composites with increased visible and near-infrared light absorption compared to the pristine support. This allows an improved overall efficiency of water oxidation (and consequently hydrogen generation at the Pt counter electrode) in passive electrolyte (pH = 7) even at 0 V bias. These low-cost and easy-to-achieve composite materials represent a promising alternative to those involving highly toxic co-catalysts. Full article

The presence of engineered nanoparticles (ENPs) in soil systems can modify their properties and the availability of nutrients. This study evaluated the effect of 1% CuO or ZnO ENPs on the physicochemical properties and on the phosphorus (P) adsorption–desorption processes of a volcanic ash soil (Lautaro; LAU). The dynamics of P were conducted through kinetic and isotherm batch experiments. The results showed that LAU soil with 1% CuO or ZnO ENPs increased pH_H2O (from 5.67 to 6.03 and 6.82, respectively), electrical conductivity (from 0.119 to 0.143 and 0.150 dS m⁻¹, respectively), Zn availability (597.7 times higher for LAU with 1% ZnO ENPs in relation to soil without ENPs), and Cu availability (41.8 times higher for LAU with 1% CuO ENPs in relation to soil without ENPs). Moreover, the presence of ENPs decreased Brunauer, Emmett, and Teller specific surface area. The adsorption kinetic studies of P on LAU soil without and with 1% ENPs fitted well to the Elovich model (r² ≥ 0.923), which indicated a chemiadsorption mechanism, whereas the adsorption isotherms were described by Langmuir–Freundlich model (r² ≥ 0.939). The desorption percentage was LAU > LAU + 1% CuO–ENPs > LAU + 1% ZnO–ENPs, demonstrating an increased stability of the P–soil surface binding with 1% ENPs. Co–existing NO₃⁻, SeO₄²⁻, and SO₄²⁻ anions did not generate a steric hindrance between P and LAU soil binding. Finally, both ENPs could alter the quality of the soil due to changes in their physicochemical properties and decrease the availability of P in volcanic ash soils. Full article

This study evaluates the preparation of novel ternary functional adsorbents based on polyaniline, zinc oxide nanoparticles, and moringa oleifera gum to produce zinc oxide/Moringa oleifera gum-grafted L-methionine-functionalized polyaniline bionanocomposites (ZM-g-Pani) and employed to sequestrate divalent metal ions (Cd²⁺, Hg²⁺ and Pb²⁺) from wastewater samples. The morphological and structural properties of ZM-g-Pani were exploited using FT-IR, FE-SEM/EDS, TEM, and XRD. FT-IR and FE-SEM studies show that the as prepared nanocomposite has an abundant number of reactive groups and a porous structure, thus demonstrating outstanding divalent metal cation removal. FT-IR study confirms that the attachment of L-methionine to polyaniline is facilitated by the C-S linkage. Both TEM and FE-SEM techniques confirmed the clustered granules of ZnO over the surface of polyaniline, which ultimately provided more surface area to adsorb metal ions. The study demonstrated that Cd²⁺, Hg²⁺ and Pb²⁺ ions could undergo physical sorption and chemisorption simultaneously during the adsorption process. The maximum adsorption capacity was 840.33, 497.51, and 497.51 mg/g for Cd²⁺, Hg²⁺, and Pb²⁺, respectively. The impact of co-existing ions, including NO₃⁻, PO₄³⁻, SO₄²⁻, Cl⁻, Na⁺, Cu²⁺, and Al³⁺, showed that there were no notable alterations in the adsorption of the selected metal ions with ZM-g-Pani. ZM-g-Pani showed eight successive regeneration cycles for Cd²⁺, Hg²⁺, and Pb²⁺ with more than 85% removal efficiency. Full article