Search Results (200)

The rapid and accurate detection of pathogenic bacteria and viruses is critical for infectious disease control and public health protection. While conventional methods (e.g., culture, microscopy, serology, and PCR) are widely used, they are often limited by lengthy processing times, high costs, and specialized equipment requirements. In recent years, metal nanocluster (MNC)-based biosensors have emerged as powerful diagnostic platforms due to their unique optical, catalytic, and electrochemical properties. This systematic review comprehensively surveys advancements in MNC-based biosensors for bacterial and viral pathogen detection, focusing on optical (colorimetric and fluorescence) and electrochemical platforms. Three key aspects are emphasized: (1) detection mechanisms, (2) nanocluster types and properties, and (3) applications in clinical diagnostics, environmental monitoring, and food safety. The literature demonstrates that MNC-based biosensors provide high sensitivity, specificity, portability, and cost-efficiency. Moreover, the integration of nanotechnology with biosensing platforms enables real-time and point-of-care diagnostics. This review also discusses the limitations and future directions of the technology, emphasizing the need for enhanced stability, multiplex detection capability, and clinical validation. The findings offer valuable insights for developing next-generation biosensors with improved functionality and broader applicability in microbial diagnostics. Full article

Background/Objectives: Airborne viral diseases pose a health risk, due to which there is a growing interest in developing filter materials capable of capturing fine particles containing virions from the air and that also have a virucidal effect. Nanofiber membranes made of poly(vinylidene fluoride) dissolved in N,N-dimethylacetamide and functionalized with copper, silver, and zinc nanoclusters were fabricated via electrospinning. This study aims to evaluate and compare the virucidal effects of nanofibers functionalized with metal nanoclusters against the human influenza A virus A/WSN/1933 (H1N1) and SARS-CoV-2. Methods: A comprehensive characterization of materials, including X-ray diffraction, scanning electron microscopy, microwave plasma atomic emission spectroscopy, thermogravimetric analysis, contact angle measurements, nitrogen sorption analysis, mercury intrusion porosimetry, filtration efficiency, and virucidal tests, was used to understand the interdependence of the materials’ physical characteristics and biological effects, as well as to determine their suitability for application as antiviral materials in air filtration systems. Results: All the filter materials tested demonstrated very high particle filtration efficiency (≥98.0%). The material embedded with copper nanoclusters showed strong virucidal efficacy against the SARS-CoV-2 alpha variant, achieving an approximately 1000-fold reduction in infectious virions within 12 h. The fibrous nanowire polymer functionalized with zinc nanoclusters was the most effective material against the human influenza A virus strain A/WSN/1933 (H1N1). Conclusions: The materials with Cu nanoclusters can be used with high efficiency to passivate and kill the SARS-CoV-2 alpha variant virions, and Zn nanoclusters modified activated porous membranes for killing human influenza A virus A7WSN/1933 (H1N1) virions. Full article

The fundamental chemistries and electronic structures of platinum catalysts over nitrogen-doped carbon supports were examined to determine the subtle yet important roles graphitic defect-based and pyridinic defect-based nitrogen defects have in stabilizing platinum. These roles address and extend previously gathered incomplete knowledge of how combinations of graphitic defect and pyridinic defect affect the local electronic structure, leading to a greater unified understanding of platinum stability. A theoretical study was designed where different atomically sized platinum clusters were investigated over seven different nitrogen defect combinations on graphene carbon support. Differently sized platinum clusters offered parametric insights into the differences in metal–support interactions. Full article

Germanium/tin-containing silicon oxide [SiO–(GeO/SnO)] nanoclusters have been designed with different Si/Ge/Sn particles and characterized as electrodes for magnesium-ion batteries (MIBs) due to forming MgBe [SiO–GeO], MgBe [SiO–SnO], MgCa [SiO–GeO], and MgCa [SiO–SnO] complexes. In this work, alkaline earth metals of magnesium (Mg), beryllium (Be), and calcium (Ca) have been studied in hybrid Mg-, Be-, and Ca-ion batteries. An expanded investigation on H capture by MgBe [SiO–(GeO/SnO)] or MgCa [SiO–(GeO/SnO)] complexes was probed using computational approaches due to density state analysis of charge density differences (CDD), total density of states (TDOS), and electron localization function (ELF) for hydrogenated hybrid clusters of MgBe [SiO–GeO], MgBe [SiO–SnO], MgCa [SiO–GeO], and MgCa [SiO–SnO]. Replacing Si by Ge/Sn content can increase battery capacity through MgBe [SiO–GeO], MgBe [SiO–SnO], MgCa [SiO–GeO], and MgCa [SiO–SnO] nanoclusters for hydrogen adsorption processes and could improve the rate performances by enhancing electrical conductivity. A small portion of Mg, Be, or Ca entering the Si–Ge or Si–Sn layer to replace the alkaline earth metal sites could improve the structural stability of the electrode material at high multiplicity, thereby improving the capacity retention rate. In fact, the MgBe [SiO–GeO] remarks a small enhancement in charge transfer before and after hydrogen adsorption, confirming the good structural stability. In addition, [SiO–(GeO/SnO)] anode material could augment the capacity owing to higher surface capacitive impacts. Full article

The measurement of humidity is of great significance for precision instruments, semiconductor integrated circuits, and element manufacturing factories. The oxygen-containing groups and noble metals in graphene-based sensing materials can significantly influence their humidity-sensing performance. Herein, 1,3,5-benzenetricarboxylic acid-functionalized reduced graphene oxide (H3BTC-rGO) loaded with Ag nanocluster nanocomposites (H3BTC-rGO/Ag) was synthesized via a facile one-step reduction method. The H3BTC-rGO/Ag-based sensor exhibited excellent humidity-sensing performance, including a higher sensitivity of 88.9% and a faster response/recovery time of 9 s/16 s towards 50% RH than those of other GO-, rGO-, and H3BTC-rGO-based sensors. The proposed humidity sensor was tested in the range of 0% to 100% RH and showed excellent sensitivity even at a low relative humidity of 0–10% or a high relative humidity of 90–100%. In addition, the H3BTC-rGO/Ag-based sensor had excellent selectivity, reliable repeatability, and good stability over 30 days under different relative humidities. Compared with H3BTC-rGO-200, the H3BTC-rGO/Ag-0.25-based sensor exhibited a low hysteresis of less than ±5% RH. The high performance was ascribed to the high density of the carboxyl groups and good conductivity of H3BTC-rGO, as well as the catalytic role of the Ag nanoclusters, resulting in high water adsorption rates. The potential applications of the H3BTC-rGO/Ag-based humidity sensor in human exhalation monitoring are also discussed. This work provides a reference for the application of graphene-based flexible sensors in monitoring very wet and dry environments. Full article

The novel pyridine oxime-based complexing agents 2-pyridinecarboxaldehyde oxime, 2-acetylpyridine ketoxime and 2-pyridine amidoxime were synthesized for alkaline Zn-Ni alloy electrodeposition, outperforming conventional citrate/TEPA systems in corrosion resistance and microstructural control. The N,O-bidentate chelation mechanism governs metal ion reduction kinetics via diffusion-limited pathways, enabling γ-phase Ni₅Zn₂₁ intermetallic formation and nanocrystalline refinement. Electrochemical and microstructural analyses demonstrate suppressed random nucleation and hydrogen evolution side reactions, leading to enhanced charge transfer resistance and reduced corrosion current density. Notably, 2-pyridine amidoxime achieves ultrasmooth surfaces through defect-free nanocluster growth, while 2-pyridinecarboxaldehyde oxime maximizes γ-phase crystallinity. The synergy between grain boundary density and surface integrity establishes a dual protection mechanism combining barrier layer formation and active dissolution suppression. This work advances microstructure engineering via coordination chemistry, offering a breakthrough over traditional zincate electroplating for high-performance anti-corrosion coatings. Full article

Oxide dispersion-strengthened (ODS) steels are among the most promising candidate structural materials for fusion and Generation-IV (Gen-IV) fission reactors, but the ductility of ODS steels is inferior to its strength properties. Therefore, we investigate void nucleation, considered as the first step of ductile damage in metal, using molecular dynamics simulations. Given that the materials are subjected to extremely complex stress states within the reactor, we present the void nucleation process of 1–4 nm Y₂O₃ nanoclusters in bcc iron during uniaxial, biaxial, and triaxial tensile deformation. We find that the void nucleation process is divided into two stages depending on whether the dislocations are emitted. Void nucleation occurs at smaller strain in biaxial and triaxial tensile deformation in comparation to uniaxial tensile deformation. Increasing the size of clusters results in a smaller strain for void nucleation. The influence of 1 nm clusters on the process of void nucleation is slight, and the void nucleation process of 1 nm cluster cases is similar to that of pure iron. In addition, void nucleation is affected by both stress and strain concentration around the clusters, and the voids grow first in the areas of high stress triaxiality. Full article

The design of efficient hydrogen evolution reaction (HER) catalysts to minimize reaction overpotentials plays a pivotal role in advancing water electrolysis and clean energy solutions. Ru-based catalysts, regarded as potential replacements for Pt-based catalysts, face stability challenges during catalytic process. The precise regulation of metal–support interactions effectively prevents Ru nanoparticle degradation while optimizing interfacial electronic properties, enabling the simultaneous enhancement of catalytic activity and stability. Herein, we design an amorphous/crystalline support and employ in situ replacement to develop a Ru-NiP_x-Ni structure. The crystalline Ni phase with ordered atomic arrangement ensures efficient charge transport, while the amorphous phase with unsaturated dangling bonds provides abundant anchoring sites for Ru nanoclusters. This synergistic structure significantly enhances HER performance, which attains overpotentials of 19 mV at 10 mA cm⁻² and 70 mV at 100 mA cm⁻² in 1 m KOH, with sustained operation exceeding 55 h at 100 mA cm⁻². Electrochemical impedance spectroscopy analysis confirms that the Ru-NiP_x-Ni structure not only has a high density of active centers for HER, but also reduces the charge transfer resistance at the electrode–electrolyte interface, which effectively enhances HER kinetics. This study presents new directions for designing high-efficiency HER catalysts. Full article

This research introduces a novel synthetic method for introducing highly luminescent silver nanoclusters (AgNCs). The technique relies on coffee Arabica seed extraction (CSE), which is the focus of this study. Our developed and manufactured ecologically friendly approach has enhanced the selectivity of AgNCs for Hg(II) ions. The coffee extract was employed in the synthesis process to stabilize and enhance the quantity of AgNCs generated. Various advanced techniques were used to characterize the AgNCs precisely in their prepared condition concerning size, surface modification, and composition. The fluorescence quenching of the AgNCs was the mechanism via which the CSE-AgNCs reacted to the principal metal ions in the experiment. Using this sensing methodology, a very accurate and selective sensing method is provided for Hg(II) in the dynamic range of 0.117 µM to 1.4 µM, with a limit of detection (LOD) equal to 35.21 nM. Comparative research was conducted to determine how selective CSE-AgNCs are for Hg(II) ions compared to other ions. Consequently, a notable degree of selectivity of AgNCs towards these Hg(II) metal ions was achieved, allowing the sensitive detection of Hg(II) metal ions, even their interfering metal ions, in the environment. AgNCs can detect Hg(II) at acceptable values within the nanomolar range. Based on their characteristics, Hg(II) ions were detected in real samples using CSE-AgNCs. Full article

Adatoms as co-catalysts may play a key role in photocatalysis, yet control of their exact configuration remains challenging. Specifically, there is converging evidence that ultra-small structures may be optimal as co-catalysts; however, a comprehensive distinction between single atoms (SAs), sub-nanoclusters (SNCs), and quantum-sized small particles (QSSPs) has yet to be established. Herein, we present a critical review addressing these distinctions, along with challenges related to the controlled synthesis of SAs, SNCs, and QSSPs; their detection methods; and their functional benefits in photocatalysis. Our discussion focuses on perovskite oxides (e.g., such as ABO₃, where A and B are cations) and metal oxides (M_xO_y, where M is a metal) decorated with adatoms, which demonstrate superior photocatalytic performance compared to their unmodified counterparts. Finally, we highlight cases of misinterpretation between SA, SNC, and QSSP configurations emerging from limitations in high-resolution detection techniques and synthesis methods. Full article

The early detection of genetic diseases is a critical need in modern medicine, underscoring the importance of developing deoxyribonucleic acid (DNA) biosensors. In recent years, metal nanoclusters (MNCs) have demonstrated significant potential as biosensors for DNA detection due to their ultra-small size, excellent photostability, bright photoluminescence, low toxicity and other outstanding properties. This review firstly discusses the characteristics of MNCs, which are effective in the early diagnosis of DNA diseases. Subsequently, different synthesis methods of MNCs are introduced. In the following section, DNA sensors based on different types of MNCs and their respective detection mechanisms are discussed in detail. Finally, the opportunities and challenges faced by DNA sensors based on MNCs are analyzed. Full article

Atomically precise noble metal nanoclusters protected by ligands are broadly discussed in the literature as a promising new class of materials with many interesting properties. Of those, the most prominent is the characteristic luminescence in the visible and near-infrared light. Within the plethora of conjugates of metal nanoclusters to various protective ligands, protein-enveloped systems present several unique features arising from an interplay of the nanocluster photophysics and the protein chemistry along its macromolecular dynamics. The specific properties of protein–metal nanocluster conjugates underlie various applications of these systems, especially in bioimaging. This review, in contrast to many already published, focuses on protein-protected gold nanoclusters (AuNCs) from the standpoint of the proteinaceous shell which plays a crucial role in the biocompatibility, solubility, and excellent in-solution stability of such nanohybrid complexes. Factors such as the protein’s size, structural rigidity, amino acid composition, electric charge, and the electron donor properties of composite amino acids are discussed. Full article

Metal nanoclusters (MNCs) are emerging as a novel class of luminescent nanomaterials with unique properties, bridging the gap between individual atoms and nanoparticles. Among these, DNA-templated MNCs have gained significant attention due to the synergistic combination of MNCs’ properties (such as exceptional resistance to photostability, size-tunable emission, and excellent optical characteristics) with the inherent advantages of DNA, including programmability, functional modification, molecular recognition, biocompatibility, and water solubility. The programmability and biocompatibility of DNA offer precise control over the size, shape, and composition of MNCs, leading to tunable optical, electrical, and magnetic properties. This review delves into the complex relationship between DNA sequence, structure, and the resulting MNC properties. By adjusting parameters such as DNA sequence, length, and conformation, the size, morphology, and composition of the corresponding MNCs can be fine-tuned, enabling insights into how DNA structure influences the optical, electrical, and magnetic properties of MNCs. Finally, this review highlights the remarkable versatility and latest advancements of DNA-templated MNCs, particularly in biosensing and imaging, and explores their future potential to revolutionize biomedical applications. Full article

Metal nanoclusters (NCs) are promising alternatives to organic dyes and quantum dots. These NCs exhibit unique physical and chemical properties, such as fluorescence, chirality, magnetism and catalysis, which contribute to significant advancements in biosensing, biomedical diagnostics and therapy. Through adjustments in composition, size, chemical environments and surface ligands, it is possible to create NCs with tunable optoelectronic and catalytic activity. This review focuses on the integration of aptamers with metal NCs, detailing molecular detection strategies that utilise the effect of aptamers on optical signal emission of metal NC-based biosensing systems. This review also highlights recent advancements in biosensing and biomedical applications, as well as illustrative case studies. To conclude, the strengths, limitations, current challenges and prospects for metal NC-based systems were examined. Full article

Designing and developing highly active, stable, and cost-effective hydrogen evolution reaction (HER) catalysts is crucial in the field of water electrolysis. In this study, we utilize N-doped porous carbon (CoNC) derived from zeolite imidazole metal–organic frameworks (ZIF-67) as support and prepare CoNC-Pt-IM-P via chemical impregnation (CoNC-Pt-IM) and plasma treatment. Systematic analyses reveal that calcined CoNC with pyridinic nitrogen could serve as a robust support to strongly anchor PtCo nanoclusters, while argon plasma treatment could lead to a noticeable aggregation of Co and Pt atoms so as to alter the electronic environment and enhance intrinsic HER catalytic activity. CoNC-Pt-IM-P could exhibit outstanding catalytic activity toward HER, achieving an exceptionally low overpotential of 31 mV at the current density of −10 mA cm⁻² and a Tafel slope of 36 mV dec⁻¹. At an overpotential of 50 mV, its mass activity reaches 4.90 A mg_Pt⁻¹, representing enhancements of 1.5 times compared to CoNC-Pt-IM and 12.3 times compared to commercial 20 wt% Pt/C. Furthermore, it could operate stably for over 110 h at a current density of −10 mA cm⁻², demonstrating its exceptional durability. This work uses plasma treatment to achieve the controllable aggregation of Co and Pt atoms to enhance their catalytic activity, which has the advantage of avoiding excessive particle aggregation compared to the commonly used method of high-temperature calcination. Full article