Search Results (476)

The detection of trace chemicals at low and ultra-low concentrations is critical for applications in environmental monitoring, medical diagnostics, food safety and other fields. Conventional detection techniques often lack the required sensitivity, specificity, or cost-effectiveness, making real-time, in situ analysis challenging. Surface-enhanced Raman spectroscopy (SERS) is a powerful analytical tool, offering improved sensitivity through the enhancement of Raman scattering by plasmonic nanostructures. While noble metals such as Ag and Au are currently the reference choices for SERS substrates, fabrication methods should balance enhancement efficiency, reproducibility and scalability. In this study, we propose a novel approach for SERS substrate fabrication using reactive Aerosol Jet Printing (r-AJP) as an innovative additive manufacturing technique. The r-AJP process enables in-flight Ag seed reduction and nucleation of Ag nanoparticles (NPs) by mixing silver nitrate and ascorbic acid aerosols before deposition, as suggested by computational fluid dynamics (CFD) simulations. The resulting coatings were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM) analyses, revealing the formation of nanoporous crystalline Ag agglomerates partially covered by residual matter. The as-prepared SERS substrates exhibited remarkable SERS activity, demonstrating a high enhancement factor (10⁶) for rhodamine (R6G) detection. Our findings highlight the potential of r-AJP as a scalable and cost-effective fabrication strategy for next-generation SERS sensors, paving the way for the development of a new additive manufacturing tool for noble metal material deposition. Full article

In the field of green chemistry, the development of more sustainable and cost-efficient methods for synthesizing primary amines is of paramount importance, with catalyst research being central to this effort. This work presents a facile, aqueous-phase synthesis of highly active cobalt catalysts (Co-Ph@SiO₂(x)) via pyrolysis of silica-supported cobalt–phenanthroline complexes. The optimized Co-Ph@SiO₂(900) catalyst achieved exceptional performance (>99% conversion, >98% selectivity) in the reductive amination of acetophenone to 1-phenylethanamine using NH₃/H₂. Systematic studies revealed that its exceptional performance originates from the in situ pyrolysis of the cobalt–phyllosilicate complex. This process promotes the uniform distribution of metal cobalt nanoparticles, simultaneously enhancing porosity and imparting bifunctional (acidic and basic) properties to the catalyst, resulting in outstanding catalytic activity and selectivity. The catalyst demonstrated broad applicability, efficiently converting diverse ketones (aryl-alkyl, dialkyl, bioactive) and aldehydes (halogenated, heterocyclic, biomass-derived) into primary amines with high yields (up to 99%) and chemoselectivity (>40 examples). This sustainable, non-noble metal-based catalyst system offers significant potential for industrial primary amine synthesis and provides a versatile tool for developing highly selective and active heterogeneous catalysts. Full article

Glancing Angle Deposition (GLAD) has emerged as a versatile and powerful nanofabrication technique for developing next-generation gas sensors by enabling precise control over nanostructure geometry, porosity, and material composition. Through dynamic substrate tilting and rotation, GLAD facilitates the fabrication of highly porous, anisotropic nanostructures, such as aligned, tilted, zigzag, helical, and multilayered nanorods, with tunable surface area and diffusion pathways optimized for gas detection. This review provides a comprehensive synthesis of recent advances in GLAD-based gas sensor design, focusing on how structural engineering and material integration converge to enhance sensor performance. Key materials strategies include the construction of heterojunctions and core–shell architectures, controlled doping, and nanoparticle decoration using noble metals or metal oxides to amplify charge transfer, catalytic activity, and redox responsiveness. GLAD-fabricated nanostructures have been effectively deployed across multiple gas sensing modalities, including resistive, capacitive, piezoelectric, and optical platforms, where their high aspect ratios, tailored porosity, and defect-rich surfaces facilitate enhanced gas adsorption kinetics and efficient signal transduction. These devices exhibit high sensitivity and selectivity toward a range of analytes, including NO₂, CO, H₂S, and volatile organic compounds (VOCs), with detection limits often reaching the parts-per-billion level. Emerging innovations, such as photo-assisted sensing and integration with artificial intelligence for data analysis and pattern recognition, further extend the capabilities of GLAD-based systems for multifunctional, real-time, and adaptive sensing. Finally, current challenges and future research directions are discussed, emphasizing the promise of GLAD as a scalable platform for next-generation gas sensing technologies. Full article

The development of non-noble metal catalysts for gas-phase propylene epoxidation with H₂/O₂ remains challenging due to their inadequate activity and stability. Herein, we report a Cs⁺-modified Ni/TS-1 catalyst (9%Ni-Cs/TS-1), which exhibits unprecedented catalytic performance, giving a state-of-the-art PO formation rate of 382.9 g_PO·kg_cat⁻¹·h⁻¹ with 87.8% selectivity at 200 °C. The catalyst stability was sustainable for 150 h, far surpassing reported Ni-based catalysts. Ni/TS-1 exhibited low catalytic activity. However, the Cs modification significantly enhanced the performance of Ni/TS-1. Furthermore, the intrinsic reason for the enhanced performance was elucidated by multiple techniques such as XPS, N₂ physisorption, TEM, ²⁹Si NMR, NH₃-TPD-MS, UV–vis, and so on. The findings indicated that the incorporation of Cs⁺ markedly boosted the reduction of Ni, enhanced Ni⁰ formation, strengthened Ni-Ti interactions, reduced acid sites to inhibit PO isomerization, improved the dispersion of Ni nanoparticles, reduced particle size, and improved the hydrophobicity of Ni/TS-1 to facilitate propylene adsorption/PO desorption. The 9%Ni-Cs/TS-1 catalyst demonstrated exceptional performance characterized by a low cost, high activity, and long-term stability, offering a viable alternative to Au-based systems. Full article

It is difficult to simultaneously achieve surface-enhanced Raman scattering (SERS) and surface-enhanced fluorescence (SEF) for noble metals. Herein, a composite substrate is demonstrated based on the rational construction of Ag nanoparticles (Ag NPs) and inverse opal polydimethylsiloxane (PDMS) for surface Raman fluorescence dual enhancement. The well-designed Ag nanoparticle (Ag NP)-decorated inverse opal PDMS (AIOP) composite substrate is fabricated using the polystyrene (PS) photonic crystal method and the sensitization reduction technique. The inverse opal PDMS enhances the electromagnetic (EM) field by increasing the loading of Ag NPs and plasmonic coupling of Ag NPs, leading to SERS activity. The thin shell layer of polyvinyl pyrrolidone (PVP) in core–shell Ag NPs isolates the detected molecule from the Ag core to prevent the fluorescence resonance energy transfer and charge transfer to eliminate fluorescence quenching and enable SEF performance. Based on the blockage of the core–shell structure and the enhanced EM field originating from the inverse opal structure, the as-fabricated AIOP composite substrate shows dual enhancement in surface Raman fluorescence. The AIOP composite substrate in this work, which combines improved SERS activity and SEF performance, not only promotes the development of surface-enhanced spectroscopy but also shows promise for applications in flexible sensors. Full article

This paper presents the synthesis of La₂Ti₂O₇ nanoparticles by the sol–gel method starting from lanthanum nitrate and titanium alkoxide (noted as LTA). Subsequently, the lanthanum titanium oxide nanoparticles are modified with noble metals (platinum) using the chemical impregnation method, followed by a reduction process with NaBH₄. The comparative analysis of the structure and surface characteristics of the nanopowders subjected to thermal treatment at 900 °C is conducted using Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) with energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray fluorescence (XRF), ultraviolet-visible (UV–Vis) spectroscopy, as well as specific surface area and porosity measurements. The photocatalytic activity is evaluated in the oxidative photodegradation of ethanol (CH₃CH₂OH) under simulated solar irradiation. The modified sample shows higher specific surfaces areas and improved photocatalytic properties, proving the better conversion of CH₃CH₂OH than the pure sample. The highest conversion of ethanol (29.75%) is obtained in the case of LTA-Pt after 3 h of simulated solar light irradiation. Full article

To successfully prepare cellulose hydrogels through a dissolution–regeneration process, 60 wt% LiBr aqueous solution was used as a green solvent. Carboxyl groups were precisely introduced onto the surface of the cellulose hydrogels through a TEMPO-mediated oxidation reaction, while the three-dimensional network structure and open pore morphology were completely retained. This modification strategy significantly enhanced the loading capacity of the hydrogels with copper nanoparticles (Cu NPs). The experimental results show that the LiBr aqueous solution can efficiently dissolve cellulose, and the TEMPO oxidation introduces carboxyl groups without destroying the stability of the hydrogels. Cu NPs are uniformly dispersed and highly loaded on the surface of the hydrogel because of the anchoring effect of the carboxyl groups. Cu NP-loaded hydrogels exhibit excellent catalytic activity in the NaBH₄ reduction of 4-nitrophenol (4-NP). Cu NP-loaded hydrogels maintain their complete structure and good catalytic performance after five consecutive cycles. Moreover, Cu NP-loaded hydrogels demonstrate high efficiency in degrading organic dyes such as methyl orange and Congo red. This study successfully developed efficient, low-cost, and environmentally friendly Cu NP-loaded hydrogel catalysts through the synergistic effect of LiBr green solvent and TEMPO oxidation modification, providing a feasible alternative to noble metal catalysts. Full article

Acetone detection is crucial for non-invasive health monitoring and environmental safety, so there is an urgent demand to develop high-performance gas sensors. Here, platinum (Pt)-functionalized layered flower-like nickel ferrite (NiFe₂O₄) sheets were efficiently fabricated via facile hydrothermal synthesis and wet chemical reduction processes. When the Ni/Fe molar ratio is 1:1, the sensing material forms a Ni/NiO/NiFe₂O₄ composite, with performance further optimized by tuning Pt loading. At 1.5% Pt mass fraction, the sensor shows a high acetone response (R_g/R_a = 58.33 at 100 ppm), a 100 ppb detection limit, fast response/recovery times (7/245 s at 100 ppm), and excellent selectivity. The enhancement in performance originates from the synergistic effect of the structure and Pt loading: the layered flower-like morphology facilitates gas diffusion and charge transport, while Pt nanoparticles serve as active sites to lower the activation energy of acetone redox reactions. This work presents a novel strategy for designing high-performance volatile organic compound (VOC) sensors by combining hierarchical nanostructured transition metal ferrites with noble metal modifications. Full article

The electrocatalytic reduction of nitrate is an efficient and green method for NH₃ production. In this study, a Co-containing MOF with a stable three-dimensional carbon framework that offers abundant metal active sites is prepared as a precursor to a Co-N-C electrocatalyst. Facile pyrolysis of the three-dimensional MOF affords the desired Co-N-C electrocatalyst, which exhibits excellent stability, an NH₃ yield of 1.12 mmol h⁻¹ mg⁻¹, and faradaic efficiency of 86.7% at −0.23 V in a 0.1 M KOH/0.1 M KNO₃. The excellent activity and durability are ascribed to the highly exposed active centres, large surface area, and high porosity structure. N doping allows the electronic properties to be modulated and provides outstanding stability owing to the strong interaction between the nitrogen-doped carbon support and Co nanoparticles. This study presents a simple and efficient synthesis strategy for the production of non-noble-metal electrocatalysts with abundant active sites for the nitrate reduction reaction. Full article

Supported Pd-based catalysts have been widely applied in the hydrogenation of specific functional groups. Recent trends have focused on employing Pd-based heterogeneous catalysts supported on inorganic nanotubes, wherein inner surface functionalization modulates both palladium nanoparticle (Pd-NP) dispersion and the interaction between reactants and the catalyst surface, thereby influencing catalytic properties. This study aims to develop a catalytic system using amine-lumened halloysite nanotubes immobilizing Pd-NPs (Pd/HNTA) as catalysts for hydrogenation reactions. The formation of Pd-NPs within the organo-functionalized lumen—modified by 3-aminopropyltrimethoxysilane—is confirmed by transmission electron microscopy (TEM) imaging, which reveals a particle size of 2.2 ± 0.4 nm. For comparison, Pd-NPs supported on pristine halloysite (Pd/HNTP) were used as control catalysts, displaying a metal particle size of 2.8 ± 0.8 nm and thereby demonstrating the effect of organic functionalization on the halloysite nanotubes. Both catalysts were employed in the hydrogenation of furfural (FUR) and nitrobenzene (NB) as model reactions. Pd/HNTA demonstrated superior catalytic performance for both substrates, with TOF values of 880 h⁻¹ for FUR and 946 h⁻¹ for NB, and selectivities exceeding 98% for tetrahydrofurfuryl alcohol (THFOH) and aniline (AN), respectively. However, recyclability studies displayed that Pd/HNTA was deactivated at the 10 catalytic cycles during the hydrogenation of FUR, whereas, in the hydrogenation of NB, 5 catalytic cycles were achieved with maximum conversion and selectivity at 360 min. These results revealed that the liquid-phase environment plays a pivotal role in catalyst stability. In the hydrogenation of NB, the coproduction of H₂O adversely affects the interaction between the Pd particles and the inner amine-modified surface, increasing the deactivation of the catalyst with reuse. Thus, the Pd/HNTA catalyst holds significant promise for the development of noble-metal-based catalysts and their application in the transformation of other reducible organic functional groups via hydrogenation reaction. Full article

Non-radiative decay of surface plasmon (SP) offers a novel paradigm for efficient conversion of photons into carriers. However, the narrow bandwidth of SP has been a significant obstacle to the widespread applications. Previously, research and applications mainly focused on noble metals such as Au, Ag, and Cu. In this article, we report an Ag-Al alloy material, μ-Ag₃Al, in which the surface plasmon operating bandwidth is 1.7 times that of Ag and hot carrier transport properties are comparable with those of AuAl. The results show that μ-Ag₃Al allows efficient direct interband electronic transitions from ultraviolet (UV) to near infrared range. Spherical nanoparticles of μ-Ag₃Al exhibit the localized surface plasmon resonance (LSPR) effect in the ultraviolet region. Its surface plasmon polariton (SPP) shows strong non-radiative decay at 3.36 eV, which is favorable for the generation of high-energy hot carriers. In addition, the penetration depth of SPP in μ-Ag₃Al remains high across the UV to the near-infrared range. Moreover, the transport properties of hot carriers in μ-Ag₃Al are comparable with those in Al, borophene and Au-Al intermetallic compounds. These properties can provide guidance for the design of plasmon-based photodetectors, solar cells, and photocatalytic reactors. Full article

Colloidal noble metal nanoparticle aggregates have demonstrated significant advantages in surface-enhanced Raman scattering (SERS) analysis, particularly for online detection, due to their excellent optical properties, spatial homogeneity, and fluidic compatibility. However, conventional chemically induced aggregation methods (such as salt-induced nanoparticle aggregation) suffer from uncontrolled aggregation, limited stability, and narrow detection windows, which restrict their quantitative and long-term applications. In this study, we developed a non-chemical method for fabricating stable colloidal aggregates from uniform β-cyclodextrin-stabilized silver nanoparticles (β-CD@AgNPs) via centrifugation. By precisely controlling the addition rate of silver nitrate, we synthesized β-cyclodextrin-stabilized silver nanoparticles with a uniform size. Surprisingly, these nanoparticles can form highly dispersed and homogeneous colloidal aggregates simply via centrifugation, which is completely different from the behavior of traditional ligand-modified nanoparticles. Notably, the resulting aggregates exhibit excellent SERS enhancement, enabling the sensitive detection of various dyes at nanomolar levels. Furthermore, they maintain a stable SERS signal (RSD = 6.99%) over a detection window exceeding 1 h, markedly improving signal stability and reproducibility compared with salt-induced aggregates. Additionally, using pyocyanin as a model analyte, we evaluated the quantitative performance of these aggregates (LOD = 0.2 nM), achieving satisfactory recovery (82–117%) in spiked samples of drinking water, lake water, and tap water. This study provides a facile strategy for fabricating stable colloidal SERS substrates and paves the way for the advancement of SERS applications in analytical sciences. Full article

Semiconductor photonic nanowires are critical components for nanoscale light manipulation in integrated photonic and electronic devices. Optimizing their optical performance requires enhanced photon conversion efficiency, for which a promising solution is to combine semiconductors with noble metals, using the surface plasmon resonance of noble metals to enhance the photon absorption efficiency. Here, we report plasmon-enhanced light emission in a hybrid nanowire device composed of perovskite semiconductor nanowires and silver nanoparticles formed using superfluid helium droplets. A cesium lead halide perovskite-based four-layer structure (CsPbBr₃/PMMA/Ag/Si) effectively reduces the metal’s plasmonic losses while ensuring efficient surface plasmon–photon coupling at moderate power. Microphotoluminescence and time-resolved spectroscopy techniques are used to investigate the optical properties and emission dynamics of carriers and excitons within the hybrid device. Our results demonstrate an intensity enhancement factor of 29 compared with pure semiconductor structures at 4 K, along with enhanced carrier recombination dynamics due to plasmonic interactions between silver nanoparticles and perovskite nanowires. This work advances existing approaches for exciting photonic nanowires at low photon densities, with potential applications in optimizing single-photon excitations and emissions for quantum information processing. Full article

Metal–organic frameworks (MOFs) or coordination polymers have gained enormous interest in recent years due to their extraordinary properties, including their high surface area, tunable pore size, and ability to form nanocomposites with various functional materials. MOF materials possess redox-active properties that are beneficial for electrochemical sensing applications. Furthermore, the tunable pore size and high surface area improve the adsorption or immobilization of enzymes, which can enhance the sensitivity and selectivity for specific analytes. Additionally, MOF-derived metal sulfides, phosphides, and nitrides demonstrate superior electrical conductivity and structural stability, ideal for electrochemical sensing. Moreover, the functionalization of MOFs further increases sensitivity by enhancing electrode–analyte interactions. The inclusion of carbon materials within MOFs enhances their electrical conductivity and reduces background current through optimized loading, preventing agglomeration and ensuring uniform distribution. Noble metals immobilized on MOFs offer improved stability and catalytic performance, providing larger surface areas and uniform nanoparticle dispersion. This review focuses on recent developments in MOF-based biosensors specifically for glucose, dopamine, H₂O₂, ascorbic acid, and uric acid sensing. Full article

The optical sensing of chirality is widely used in many fields, such as pharmaceuticals, agriculture, food, and environmental materials. In this context, the color-based cascade amplification of chirality, coupled with chiral recognition for analytes, provides a low-cost and straightforward detection method that avoids the use of expensive and sophisticated instrumentation. However, the realization of chiral detection using this approach is still challenging because the construction of a three-dimensional optical recognition site is required to easily discern differences in chirality. Therefore, considerable efforts have been dedicated to developing a hierarchical approach based on molecular organization to provide colorimetric sensors for chirality detection. This review covers function-integrated molecular sensors with colorimetric responsive sites based on absorption, fluorescence, and aggregation-induced emission enabled by molecular organization. In line with the hierarchical approach, data-driven chemometrics is a useful method for quantitative and accurate chiral pattern recognition. Finally, colorimetric nanomaterials are discussed, focusing on sensing platforms using noble-metal nanoparticles, carbon dots, and photonic crystal gels. Full article