Search Results (149)

Electrochemical CO₂ reduction reaction (CO₂RR) is a key technology for achieving carbon neutrality and efficient utilization of renewable energy, capable of converting CO₂ into high-value-added carbon-based fuels and chemicals. Copper (Cu)-based catalysts have attracted significant attention due to their unique performance in generating multi-carbon (C₂₊) products such as ethylene and ethanol; however, there are still many controversies regarding their complex reaction mechanisms, active sites, and the dynamic evolution of intermediates. In situ Raman spectroscopy, with its high surface sensitivity, applicability in aqueous environments, and precise detection of molecular vibration modes, has become a powerful tool for studying the structural evolution of Cu catalysts and key reaction intermediates during CO₂RR. This article reviews the principles of electrochemical in situ Raman spectroscopy and its latest developments in the study of CO₂RR on Cu-based catalysts, focusing on its applications in monitoring the dynamic structural changes of the catalyst surface (such as Cu⁺, Cu⁰, and Cu²⁺ oxide species) and identifying key reaction intermediates (such as *CO, *OCCO(*O=C-C=O), *COOH, etc.). Numerous studies have shown that Cu-based oxide precursors undergo rapid reduction and surface reconstruction under CO₂RR conditions, resulting in metallic Cu nanoclusters with unique crystal facets and particle size distributions. These oxide-derived active sites are considered crucial for achieving high selectivity toward C₂₊ products. Time-resolved Raman spectroscopy and surface-enhanced Raman scattering (SERS) techniques have further revealed the dynamic characteristics of local pH changes at the electrode/electrolyte interface and the adsorption behavior of intermediates, providing molecular-level insights into the mechanisms of selectivity control in CO₂RR. However, technical challenges such as weak signal intensity, laser-induced damage, and background fluorescence interference, and opportunities such as coupling high-precision confocal Raman technology with in situ X-ray absorption spectroscopy or synchrotron radiation Fourier transform infrared spectroscopy in researching the mechanisms of CO₂RR are also put forward. Full article

Efficient use of nitrogen and phosphorus is crucial for achieving sustainable wheat production. Slow-release nano-fertilizers offer a targeted strategy to minimize nutrient losses, reduce excessive fertilizer application, and improve crop yield. This study introduces urea–hydroxyapatite (n-UHA) nanohybrid as a slow-release fertilizer synthesized to enhance nitrogen (N) and phosphorus (P) delivery efficiency in wheat (Triticum aestivum L.). Physical characterization techniques, including Scanning Electron Microscopy (SEM), Energy-Dispersive X-ray Spectroscopy (EDS), Zetasizer, and Fourier Transform Infrared Spectroscopy (FTIR), confirmed the formation of spherical n-UHA with a particle size of 106 nm. FTIR results indicated the formation of physically bound urea as a coating layer on the particle surface. Foliar application of n-UHA at 2500 and 5000 ppm N significantly increased tiller intensity and grain yield compared to conventional urea. The highest biological yield, approximately 16 t ha⁻¹, was achieved with 5000 ppm n-UHA plus supplemental soil phosphorus (P), representing a 4-fold increase over the control. Conventional urea treatments, in comparison, only doubled yield. Notably, increasing conventional urea concentration from 2500 to 5000 ppm N did not significantly increase the yield even with additional P-soil supplement, while applying 5000 ppm N from n-UHA with supplemental P provided an approximate 25% yield increase compared to 2500 ppm n-UHA without P. The n-UHA’s slow-release mechanism supported prolonged tiller intensity, enhanced protein content, and higher biomass yield and chlorophyll content. This study showed that the slow-release mechanism of urea in the monohybrid due to hydrolysis resulted in localized acidity from carbonic acid production on the leaf surface area and contributed to dissociating phosphate ions from hydroxyapatite, making phosphorous more accessible. The enhanced performance of n-UHA is due to its controlled nutrient release, enabled by the physical binding of urea with hydroxyapatite nanoparticles. This binding ensures a synchronized supply of nitrogen and phosphorus aligned with plant demand. The nano-hydroxyapatite composite (N/Ca 6:1) supplies balanced nutrients via efficient stomatal absorption and gradual release. As an eco-friendly alternative to conventional fertilizers, n-UHA improves nitrogen delivery efficiency and reduces N-evaporation, supporting sustainable agriculture. Full article

Agricultural nondestructive testing technology is pivotal in safeguarding food quality assurance, safety monitoring, and supply chain transparency. While conventional optical methods such as near-infrared spectroscopy and hyperspectral imaging demonstrate proficiency in surface composition analysis, their constrained penetration depth and environmental sensitivity limit effectiveness in dynamic agricultural inspections. This review highlights the transformative potential of microwave technologies, systematically examining their operational principles, current implementations, and developmental trajectories for agricultural quality control. Microwave technology leverages dielectric response mechanisms to overcome traditional limitations, such as low-frequency penetration for grain silo moisture testing and high-frequency multi-parameter analysis, enabling simultaneous detection of moisture gradients, density variations, and foreign contaminants. Established applications span moisture quantification in cereal grains, oilseed crops, and plant tissues, while emerging implementations address storage condition monitoring, mycotoxin detection, and adulteration screening. The high-frequency branch of the microwave–millimeter wave systems enhances analytical precision through molecular resonance effects and sub-millimeter spatial resolution, achieving trace-level contaminant identification. Current challenges focus on three areas: excessive absorption of low-frequency microwaves by high-moisture agricultural products, significant path loss of microwave high-frequency signals in complex environments, and the lack of a standardized dielectric database. In the future, it is essential to develop low-cost, highly sensitive, and portable systems based on solid-state microelectronics and metamaterials, and to utilize IoT and 6G communications to enable dynamic monitoring. This review not only consolidates the state-of-the-art but also identifies future innovation pathways, providing a roadmap for scalable deployment of next-generation agricultural NDT systems. Full article

Potassium bromide (KBr) thin films were deposited by resistive thermal evaporation at substrate temperatures ranging from 50 °C to 250 °C to systematically elucidate the temperature-dependent evolution of their physical properties. Structural, morphological, and optical characteristics were examined by X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM), and Fourier transform infrared spectroscopy (FTIR). The results reveal a complex, non-monotonic response to temperature rather than a simple linear trend. As the substrate temperature increases, growth evolves from a mixed polycrystalline texture to a pronounced (200) preferred orientation. Morphological analysis shows that the film surface is smoothest at 150 °C, while the microstructure becomes densest at 200 °C. These structural variations directly modulate the optical constants: the refractive index attains its highest values in the 150–200 °C window, approaching that of bulk KBr. Cryogenic temperature (6 K) FTIR measurements further demonstrate that suppression of multi-phonon absorption markedly enhances the infrared transmittance of the films. Taken together, the data indicate that 150–200 °C constitutes an optimal process window for fabricating KBr films that combine superior crystallinity, low defect density, and high packing density. This study elucidates the temperature-driven structure–property coupling and offers valuable guidance for optimizing high-performance infrared and cryogenic optical components. Full article

In this study, Bacillus tropicus (BT), a non-toxic and eco-friendly microorganism, was employed to substitute traditional inorganic depressants in the flotation separation of copper-molybdenum sulfides. Single mineral flotation tests were performed to examine BT’s impact on the flotation behavior of molybdenite and chalcopyrite. The results indicated that excessive BT inhibited the flotation of both minerals, reducing their recoveries below 40%. At a BT dosage of 2.5 kg/t and pH 9.0, chalcopyrite recovery was 74.10%, while molybdenite recovery was 20.47%, achieving an effective separation of the two minerals. BT’s adsorption mechanism on molybdenite and chalcopyrite was analyzed through contact angle tests, thermogravimetric analysis, and Fourier transform infrared spectroscopy. These analyses revealed that increased BT absorption on molybdenite enhanced its surface hydrophilicity. This research offers a novel perspective on utilizing microorganisms as efficient flotation reagents. Full article

To investigate the impermeability of foam concrete in various challenging environments, this study evaluates its water resistance by measuring the water contact angle and water absorption. Polyurethane (PU) was used to fabricate polyurethane foam concrete (PFC), enabling a monolithic hydrophobic modification to improve the permeation performance of foam concrete. The study also examines the effects of carbonation and freeze–thaw environments on the permeation resistance of PFC. Graphene oxide (GO), KH-550, and a composite hydrophobic coating (G/S) consisting of GO and KH-550 were employed to enhance the permeation resistance of PFC through surface hydrophobic modification. The functionality of the G/S composite hydrophobic coating was confirmed using energy dispersive X-ray spectrometry (EDS) and Fourier transform infrared spectroscopy (FTIR). The results showed the following: (1) The water contact angle of PFC increased by 20.2° compared to that of ordinary foam concrete, indicating that PU-based hydrophobic modification can significantly improve its impermeability. (2) After carbonation, a micro–nano composite structure resembling the surface of a lotus leaf developed on the surface of PFC, further enhancing its impermeability. However, freeze–thaw cycles led to the formation and widening of microcracks in the PFC, which compromised its hydrophobic properties. (3) Surface hydrophobic modifications using GO, KH-550, and the G/S composite coating improved the anti-permeability properties of PFC, with the G/S composite showing the most significant enhancement. (4) GO filled the tiny voids and pores on the surface of the PFC, thereby improving its anti-permeability properties. KH-550 replaced water on the surface of PFC and encapsulated surface particles, orienting its R-groups outward to enhance hydrophobicity. The G/S composite emulsion coating formed a hydrophobic silane layer inside the concrete, which enhanced water resistance by blocking water penetration, reducing microscopic pores in the hydrophobic layer, and improving impermeability characteristics. Full article

Optical sensors have undergone significant evolution, transitioning from discrete optical microsystems toward sophisticated photonic integrated circuits (PICs) that leverage artificial intelligence (AI) for enhanced functionality. This review systematically explores the integration of optical sensing technologies with AI, charting the advancement from conventional optical microsystems to AI-driven smart devices. First, we examine classical optical sensing methodologies, including refractive index sensing, surface-enhanced infrared absorption (SEIRA), surface-enhanced Raman spectroscopy (SERS), surface plasmon-enhanced chiral spectroscopy, and surface-enhanced fluorescence (SEF) spectroscopy, highlighting their principles, capabilities, and limitations. Subsequently, we analyze the architecture of PIC-based sensing platforms, emphasizing their miniaturization, scalability, and real-time detection performance. This review then introduces the emerging paradigm of in-sensor computing, where AI algorithms are integrated directly within photonic devices, enabling real-time data processing, decision making, and enhanced system autonomy. Finally, we offer a comprehensive outlook on current technological challenges and future research directions, addressing integration complexity, material compatibility, and data processing bottlenecks. This review provides timely insights into the transformative potential of AI-enhanced PIC sensors, setting the stage for future innovations in autonomous, intelligent sensing applications. Full article

To elucidate the modification mechanism of waterborne polyurethane (WPU) on emulsified asphalt, anionic and cationic WPUs are utilized as modifiers. As well, their effects on physical properties, microstructure, and compatibility are characterized using basic performance tests, Fourier transform infrared spectroscopy (FTIR), and atomic force microscopy (AFM). The results show that WPU-modified emulsified asphalt exhibited a higher softening point, reduced penetration, and decreased ductility, suggesting enhanced high-temperature stability but diminished low-temperature flexibility. Among all samples, the combination of cationic WPU with cationic emulsified asphalt shows the highest softening point (54.1 °C), whereas cationic emulsified asphalt alone exhibits the lowest one (52.9 °C). Anionic emulsified asphalt demonstrates the highest penetration (79 mm), while non-ionic WPU combined with cationic emulsified asphalt shows the lowest one (59.3 mm). The ductility decreases from 90.3 cm to 28.7 cm. The storage stability varies with WPU ion type. Cationic WPU-modified samples showed the poorest storage stability (0.7% residue), while anionic-modified samples exhibit the best one (0.4% residue). FTIR analysis confirms the presence of characteristic WPU absorption peaks, indicating that physical blending occurs, and chemical interaction is limited. AFM observations reveal that anionic WPUs provide superior compatibility, forming fine, uniformly distributed particles with the lowest surface roughness (5.655 nm). In contrast, cationic WPUs form chain-like structures that cure effectively but exhibit poor dispersion. This study provides a basis for the development of high-performance WPU-modified emulsified asphalt. Full article

Papilloscopy, the science of human identification through fingerprints, has seen notable advancements in developing less toxic latent fingerprint developers (LFDs), especially from natural feedstock. Tannins, the second most abundant natural polyphenol, present a potential eco-friendly and cost-effective alternative, with no record of their use as LFDs in the existing literature. This study characterized four types of tannins from black wattle, using Fourier Transform Infrared Spectroscopy, revealing key functional groups like C=O, C=C, and O–H. Ultraviolet–visible absorption spectra showed similar behaviors for all tannins, indicating phenolic and benzenoid structures. Energy-dispersive X-ray Spectroscopy identified high concentrations of chlorine, sodium, potassium, and sulfur, naturally found in biomass and soil. Finally, elements in significant concentrations, such as sodium, potassium, iron, zinc, and copper, were found through the incineration of the spent bark. On the basis of these findings, the tannin with the highest potential for LFD was selected. Combining this tannin with spent bark ash resulted in a composite whose performance was evaluated using different methods, including depletion studies, tests with various donors, and assessments on different surfaces. The results demonstrated that this combination significantly enhanced the material’s efficiency by integrating organic and inorganic properties, which improved visual contrast and powder adhesion. Full article

In recent years, protecting stainless steel from corrosion has become crucial, particularly in harsh environments. The present study focuses on improving the photocathodic corrosion resistance of 304 stainless steel (304SS) by fabricating TiO₂/CuO composite coatings using the spin coating technique with varying CuO weight percentages. Structural characterization through X-ray diffraction (XRD) confirmed the presence of the anatase phase of TiO₂ and the successful integration of CuO. Raman spectroscopy demonstrated redshifts in the TiO₂ characteristic peaks, suggesting changes in bond lengths attributed to CuO incorporation. These findings were further corroborated by Fourier-transform infrared (FTIR) spectroscopy. Surface characterization showed uniform, porous coatings with pore sizes ranging from 75 to 200 nm, which contributed to improved barrier properties. UV–visible diffuse reflectance spectroscopy (UV-DRS) demonstrated enhanced visible light absorption in the heterostructures. Mott–Schottky analysis confirmed improved charge carrier density and favorable band alignment, facilitating efficient charge separation. The electrochemical performance was evaluated in 3.5% NaCl solution under dark and light environments. The results demonstrated that the TiO₂/CuO heterostructure significantly enhanced electron transfer and suppressed electron-hole recombination, providing adequate photocathodic protection. Notably, under illumination, the TiO₂/CuO (0.005 g) coating achieved a corrosion potential of −255 mV vs SCE and reduced the corrosion current density to 0.460 × 10⁻⁶ mA cm⁻². These findings suggest that TiO₂/CuO coatings offer a promising, durable, and cost-effective solution for corrosion protection in industries such as oil, shipbuilding, and pipelines. Full article

Owing to global energy demands and climate change resulting from fossil fuel use, technologies capable of converting greenhouse gases into renewable energy resources are needed. One such technology is photocatalytic CO₂ reduction, which utilises solar energy to transform CO₂ into value-added hydrocarbons. However, the application of photocatalytic CO₂ reduction is limited by the inefficiency of existing photocatalysts. In this study, we developed a nitrogen-deficient g-C₃N₄-confined PtCu dual-atom catalyst (PtCu/V_N-C₃N₄) for photocatalytic CO₂ reduction. Aberration-corrected high-angle annular dark-field scanning transmission electron microscopy and X-ray absorption fine structure spectroscopy confirmed the atomic-level anchoring of PtCu pairs onto the nitrogen-vacancy-rich g-C₃N₄ nanosheets. The optimised PtCu/V_N-C₃N₄ exhibited superior photocatalytic performance, with CO and CH₄ evolution rates of 13.3 µmol/g/h and 2.5 µmol/g/h, respectively, under visible-light irradiation. Mechanistic investigations revealed that CO₂ molecules were preferentially adsorbed onto the PtCu dual sites, initiating a stepwise reduction pathway. In situ diffuse reflectance infrared Fourier-transform spectroscopy identified the formation of a key intermediate (HCOO*), whereas interfacial wettability studies demonstrated efficient H₂O adsorption on PtCu sites, providing essential proton sources for CO₂ protonation. Photoelectrochemical characterisation further confirmed the enhanced charge-transfer kinetics in PtCu/V_N-C₃N₄, which were attributed to the synergistic interplay between the nitrogen vacancies and dual-atom sites. Notably, the dual-active-site architecture minimised the competitive adsorption between CO₂ and H₂O molecules, thereby optimising the surface reaction pathways. This study establishes a rational strategy for designing atomically precise dual-atom catalysts through defect engineering, achieving concurrent improvements in activity, selectivity, and charge carrier utilisation for solar-driven CO₂ conversion. Full article

This study employed response surface methodology to optimize the conditions for ultrahigh-pressure-assisted enzymatic extraction (UHPEE) of pectin from hawthorn using cellulase. The effects of this method on the characteristics of the extracted pectin were investigated. The optimal extraction parameters were determined to be a solid-to-liquid ratio of 1:70 g/mL, an extraction pressure of approximately 300 MPa, and a holding time of roughly 600 s, yielding a pectin recovery of 4.02%. The optimized UHPEE process resulted in reductions in both the degree of esterification and molecular weight of the pectin, while concurrently increasing the content of total galacturonic acid and total polyphenols. Ion chromatography analysis identified five monosaccharides in the hawthorn pectin, with galacturonic acid being the most predominant. Fourier-transform infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM) analyses revealed the presence of characteristic absorption peaks of pectin and a rough surface topology with a loose, flaky structure, respectively. Rheological measurements demonstrated that the hawthorn pectin exhibited shear-thinning behavior, characteristic of a pseudoplastic fluid. In vitro antioxidant assays showed that hawthorn pectin scavenged 1,1-diphenyl-2-picrylhydrazyl (DPPH) radicals with a rate of 92.72%, comparably to vitamin C at the same concentration (96.30%). These results indicate that the optimized UHPEE method is a more efficient technique for extracting hawthorn pectin and effectively enhances its antioxidant activity, suggesting its potential application in the food industry. Full article

Chemically modified starch is a widely used food additive for tailoring the quality of wheat flour products. However, the effects of octenyl succinic anhydride (OSA)-modified wheat starch with varying degrees of substitution on the quality of dough and noodles remain unclear. In this study, we prepared two types of OSA-modified wheat starch with different degrees of substitution and incorporated them as additives into a wheat starch–gluten protein model flour system to evaluate their impact on dough processing characteristics. Fourier transform infrared (FTIR) spectroscopy results revealed the introduction of ester carbonyl (C=O) and carboxylate (RCOO−) functional groups into the starch structure. X-ray diffraction (XRD) analysis demonstrated that OSA modification reduced the relative crystallinity of starch and disrupted the long-range structural order of the native starch. Scanning electron microscopy (SEM) observations indicated that the surface of OSA-modified wheat starch granules became rougher. OSA modification enhanced the solubility, water absorption capacity, and apparent viscosity but lowered the gelatinization temperature of starch, making starch more prone to gelatinization. Furthermore, the incorporation of OSA-modified wheat starch significantly altered the gelatinization behavior and dynamic rheological properties of wheat dough, whilst the noodle with the addition of OSA-modified starch (DS = 0.019) reduced the cooking time by 29.0% compared to the control group noodle and improved its water absorption rate. This study provides a theoretical foundation for the application of OSA-modified wheat starch as a food additive in wheat-based foods. Full article

In this study, a new edible gel of Perilla essential oil (PE)/grape seed extract (GSE)–chitosan/gelatin was prepared, and it was applied to the preservation of silver carp. By establishing a fuzzy mathematical model, using a single-factor experiment and Box–Behnken response surface optimization combined with matlab analysis, the optimum preparation conditions of composite gel films were determined: the addition of PE (p < 0.01) was 6.91 μL/mL, the addition of GSE (p < 0.05) was 0.45 mg/mL, and the addition of gelatin (p > 0.05) was 1.63%. Under these conditions, the composite gel films exhibited an excellent water vapor barrier and mechanical properties. Using Fourier-transform infrared spectroscopy (FTIR) analysis, it was found that the addition of PE enhanced or weakened the absorption peaks, indicating the molecular interaction between PE and the substrate. Scanning electron microscopy (SEM) observed that the surfaces of the composite gel films with added PE were smooth, but there were a few pores in the cross-section. X-ray diffraction (XRD) analysis showed that PE had good compatibility with other components. The fresh-keeping experiment showed that the composite gel films could significantly prolong the fresh-keeping period of grass carp. After 10 days of storage at 4 °C, compared with the blank group (without plastic wrap) and the control group (with composite gel film, no PE added), the experimental group (with composite gel films, PE added) showed better fresh-keeping effect in terms of sensory score, moisture content, pH value, TBARS value, and TVB-N value (p < 0.05). Correlation analysis further confirmed the positive effects of composite gel films on water content, pH value, TVB-N, and other quality indexes of silver carp, indicating that the composite gel films will have broad application prospects in the food preservation field. This study provides an innovative basis and theoretical basis for the development and application of natural polysaccharide/protein composite edible film, which is helpful to promote the development of green food-packaging materials. Full article

This study successfully prepared MIL-101(Fe)@MoS₂ composite photocatalysts via hydrothermal methods to address the efficient removal of refractory organic dyes in dye wastewater. Characterization using X-ray diffraction (XRD), Fourier transform infrared (FT-IR), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS) confirmed that molybdenum disulfide (MoS₂) was uniformly loaded onto the surface of MIL-101(Fe), forming a heterojunction that significantly enhanced light absorption capacity and charge separation efficiency. In a visible-light-driven photo-Fenton system, this material exhibited excellent degradation performance for Congo red (CR). At an initial CR concentration of 50 mg/L, a catalyst dosage of 0.2 g/L, 4 mL of added H₂O₂, and pH 7, CR was completely degraded within 30 min, with the total organic carbon (TOC) removal reaching 72.5%. The material maintained high degradation efficiency (>90%) across a pH range of 3–9, overcoming the traditional Fenton system’s dependency on acidic media. Radical-trapping experiments indicated that superoxide radicals (·O₂⁻) and photogenerated holes (·h⁺) were the primary active species responsible for degradation, revealing a synergistic catalytic mechanism at the heterojunction interface. Recyclability tests showed that the material retained 90.8% degradation efficiency after five cycles, and an X-ray photoelectron spectroscopy (XPS) analysis demonstrated the stable binding of Fe and Mo, preventing secondary pollution. This study provides a scientific basis for developing efficient, stable, and wide-pH adaptable photo-Fenton catalytic systems, contributing significantly to the advancement of green water treatment technologies. Full article