Ionic magnetic core–shell nanoparticles for DNA extraction

Magnetic nanoparticles with specific surface features are interesting materials for biomedical applications. The combination of molecular interactions on small particles with macroscopic cohesion forces offers unique opportunities. This work reports the synthesis of magnetic core–shell nanoparticles with alkylimidazolium coated surface for effective DNA extraction. A magnetic Fe₂O₃ core was coated with a silica shell and functionalized with an organic halide. This enabled a surface coating with organic cations to mediate effective molecular interactions with polyanionic DNA. The large surface area of the ∼20 nm small particles with a magnetization of 25 emu g⁻¹ enabled high DNA particle loading of 1/30 m% with easy isolation based on an external magnetic field. Moreover, the coating of the particles stabilized DNA against ultrasound initiated fragmentation.

The fabrication ionic magnetic core-shell nanoparticles were simple synthesize with a super-ferromagnetic and small particle size properties, which enabled sufficient DNA particle loading with easy isolation based on an external magnetic field.     

Colorimetric sensing of glucose and GSH using core–shell Cu/Au nanoparticles with peroxidase mimicking activity

The catalytic properties of bimetallic nanoparticles have been widely studied by researchers in many fields. In this paper, core–shell Cu/Au nanoparticles (Cu/Au NPs) were synthesized by a simple and mild one-pot method, and their peroxidase activity was proved by catalyzing the oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) with color change to blue. The change of solution color and absorbance strongly depends on the concentration of H₂O₂, so it can be used for direct detection of H₂O₂ and indirect detection of glucose. What''s more, GSH can efficiently react with the hydroxyl radicals from H₂O₂ catalyzed by core–shell Cu/Au NPs to inhibit the production of ox-TMB. Thus, the concentration of GSH can be determined by the decrease in the absorbance of the solution at 652 nm. The results showed that our proposed strategy had good detection range and detection limit for the detection of glucose and GSH. This method has been used in the detection of practical samples and has great application potential in environmental monitoring and clinical diagnosis.

Core–shell Cu/Au nanoparticles were synthesized by a one pot method, their peroxidase activity was proved by catalysing the oxidation of 3,3′,5,5′-tetramethylbenzidine with colour change to blue. Results showed a good range and limit for the detection of glucose and GSH.     

Au–Ag core–shell composite nanoparticles as a selective and sensitive plasmonic chemical probe for l-cysteine detection in Lens culinaris (lentils)

The present work reported is a simple and selective method for the colorimetrical detection of l-cysteine in Lens culinaris (or lentils) using Au–Ag core–shell (Au core Ag shell) composite nanoparticles as a chemical probe. The phenomenon is based on the color change of composite nanoparticles from yellowish brown to light blue, followed by a shift of the localized surface plasmon resonance (LSPR) absorption band in the UV-visible region (i.e., 200–800 nm) with the addition of l-cysteine into the solution of bimetallic nanoparticles. The mechanism for the detection of l-cysteine is based on the electrostatic interaction of the metal ion with the thiol group of the amino acid, which causes the red shift of the LSPR band at 685 nm. The size distribution, morphology, composition and optical properties of the Au–Ag core–shell composite nanoparticles were characterized by transmission electron microscopy (TEM), dynamic light scattering (DLS), energy dispersive X-ray diffraction (EDX), UV-visible spectrophotometer and Fourier transform infrared spectroscopy (FTIR) techniques. An excellent linearity range for the present method was observed in the range of 20–140 μg mL⁻¹ with a limit of detection at 1.95 μg mL⁻¹ and correlation coefficient (R²) of 0.986. A good% recovery of 4.0% showed the selectivity of the method for l-cysteine determination from sample matrices. The advantageous features of the present method are being simple, rapid, low cost and selectivity towards the determination of l-cysteine in lentils.

The present work reported is a simple and selective method for the colorimetrical detection of l-cysteine in Lens culinaris (or lentils) using Au–Ag core–shell (Au core Ag shell) composite nanoparticles as a chemical probe.     

Plasmonic nanoprobes based on the shape transition of Au/Ag core–shell nanorods to dumbbells for sensitive Hg-ion detection

We report a sensitive and selective localized surface plasmon resonance (LSPR) nanoprobe for the detection of mercuric ions (Hg²⁺) using gold/silver core–shell nanorods as an optical nanosubstrate. Sulfide can quickly react with silver atoms to generate Ag₂S at room temperature in the presence of oxygen. The transformation from Ag shell to Ag₂S on the nanorod surface results in its LSPR absorption band shifting to a longer wavelength, which is attributed to their different refractive indices. Interestingly, the morphology also changed from a rod-like to dumbbell shape. However, in the presence of Hg²⁺, this morphology transformation is inhibited because the sulfide reacts with free Hg²⁺ prior to the Ag atoms. The amount of Ag₂S reduced with the increasing concentration of Hg²⁺, and the absorption band shift was also decreased. According to this “rod-like to dumbbell or not” shape change, a sensitive and selective LSPR nanoprobe was established, assisted by UV-Vis absorption spectroscopy. The detection limit of this probe for Hg²⁺ was as low as 13 nM. The efficiency of this probe in complex samples was evaluated by the detection of Hg²⁺ in spiked water samples.

Sensitive plasmonic nanoprobes for the sensitive detection of mercury ions based on a “rod-like to dumbbell or not” morphology transition of the Au/Ag core–shell hybrid nanorods.     

X-ray powder diffraction to analyse bimetallic core–shell nanoparticles (gold and palladium; 7–8 nm)

A comparative X-ray powder diffraction study on poly(N-vinyl pyrrolidone) (PVP)-stabilized palladium and gold nanoparticles and bimetallic Pd–Au nanoparticles (both types of core–shell nanostructures) was performed. The average diameter of Au and Pd nanoparticles was 5 to 6 nm. The two types of core–shell particles had a core diameter of 5 to 6 nm and an overall diameter of 7 to 8 nm, i.e. a shell thickness of 1 to 2 nm. X-ray powder diffraction on a laboratory instrument was able to distinguish between a physical mixture of gold and palladium nanoparticles and bimetallic core–shell nanoparticles. It was also possible to separate the core from the shell in both kinds of bimetallic core–shell nanoparticles due to the different domain size and because it was known which metal was in the core and which was in the shell. The spherical particles were synthesized by reduction with glucose in aqueous media. After purification by multiple centrifugation steps, the particles were characterized with respect to their structural, colloid-chemical, and spectroscopic properties, i.e. particle size, morphology, and internal elemental distribution. Dynamic light scattering (DLS), differential centrifugal sedimentation (DCS), atomic absorption spectroscopy (AAS), ultraviolet-visible spectroscopy (UV-vis), high-angle annular dark field imaging (HAADF), and energy-dispersed X-ray spectroscopy (EDX) were applied for particle characterization.

A comparative X-ray powder diffraction study on poly(N-vinyl pyrrolidone) (PVP)-stabilized palladium and gold nanoparticles and bimetallic Pd–Au nanoparticles (both types of core–shell nanostructures) was performed.     

Hydrophilic and antimicrobial core–shell nanoparticles containing guanidine groups for ultrafiltration membrane modification

Physical blending is a common technique to improve the water flux and antifouling performance of ultrafiltration (UF) membranes. In the present work, a novel hydrophilic and antimicrobial core–shell nanoparticle was synthesized through the chemical grafting of poly(guanidine-hexamethylenediamine-PEI) (poly(GHPEI)) on the surface of silica nanoparticles (SNP). The synthesized core–shell nanoparticles, poly(GHPEI) functionalized silica nanoparticles (SNP@PG), were incorporated into polyethersulfone (PES) to fabricate hybrid UF membranes by a phase inversion process. The chemical composition, surface and cross section morphologies, hydrophilicity, water flux and protein rejection of the membranes were evaluated by a series of characterizations. Results show that the prepared PES/SNP@PG hybrid membrane exhibits not only improved water flux, which is around 2.6 times that of the pristine PES membrane, but also excellent resistance to organic fouling and biofouling.

Hydrophilic and antimicrobial core–shell nanoparticles containing guanidine groups (SNP@PG) were applied to fabricate membranes with improved water flux and fouling resistance.     

Sugar based cationic magnetic core–shell silica nanoparticles for nucleic acid extraction

Nucleic acid (NA) extraction is an essential step in molecular testing for a wide range of applications. Conventional extraction protocols usually suffer from time consuming removal of non-nucleic acid impurities. In this study, a new magnetic nanoparticle (MNP) is presented to simplify the NA extraction. A core–shell design, comprising of a ferromagnetic core coated with mesoporous silica, forms the basis of the functional nanoparticle. Chemical functionalization of the silica coating includes a multistep synthesis, in which an activated nanoparticle is coupled with a triethylene glycol spaced glycosyl imidazole. The molecular design aims for charge interactions between the imidazolium-based positive nanoparticle surface and nucleic acids, with specific hydrogen bonding between the surface bonded carbohydrate and nucleic acid targets to ensure nucleic acid selectivity and avoid protein contamination. Two different carbohydrates, differing in molecular size, were selected to compare the efficiency in terms of NA extraction. A triethylene glycol spacer provides sufficient flexibility to remove particle surface constraints for the interaction. The Brunauer–Emmett–Teller (BET) analysis shows a significantly larger surface area for the disaccharide-based particles NpFeSiImMalt (∼181 m² g⁻¹) compared to the monosaccharide analogue NpFeSiImGlc (∼116 m² g⁻¹) at small particles sizes (range ∼ 15 nm) and sufficient magnetization (29 emu g⁻¹) for easy isolation by an external magnetic field. The particles enabled a high DNA particle loading ratio of 30–45 wt% (MNP/DNA ratio), reflecting an efficient extraction process. A high desorption rate (7 min) with more than 86% of unchanged DNA loading was recorded, indicating low damage to the target extract.

New design of cationic magnetic core–shell nanoparticles fabricated with a large hydrophilic group (carbohydrate molecules) enabled high adsorption of a nucleic acid, easy isolation and controlled the movement by applying an external magnetic field.     

Green synthesis of biocompatible core–shell (Au–Ag) and hybrid (Au–ZnO and Ag–ZnO) bimetallic nanoparticles and evaluation of their potential antibacterial,antidiabetic, antiglycation and anticancer activities

The fabrication of bimetallic nanoparticles (BNPs) using plant extracts is applauded since it is an environmentally and biologically safe method. In this research, Manilkara zapota leaf extract was utilized to bioreduce metal ions for the production of therapeutically important core–shell Au–Ag and hybrid (Au–ZnO and Ag–ZnO) BNPs. The phytochemical profiling of the leaf extract in terms of total phenolic and flavonoid content is attributed to its high free radical scavenging activity. FTIR data also supported the involvement of these phytochemicals (polyphenols, flavonoids, aromatic compounds and alkynes) in the synthesis of BNPs. Whereas, TEM and XRD showed the formation of small sized (16.57 nm) spherical shaped core–shell Au–Ag BNPs and ZnO nano-needles with spherical AuNPs (48.32 nm) and ZnO nano-rods with spherical AgNP (19.64 nm) hybrid BNPs. The biological activities of BNPs reinforced the fact that they show enhanced therapeutic efficacy as compared to their monometallic components. All BNPs showed comparable antibacterial activities as compared to standard tetracycline discs. While small sized Au–Ag BNPs were most effective in killing human hepato-cellular carcinoma cells (HepG2) in terms of lowest cell viability, highest intracellular ROS/RNS production, loss of mitochondrial membrane potential, induction of caspase-3 gene expression and enhanced caspase-3/7 activity. BNPs also effectively inhibited advanced glycation end products and carbohydrate digesting enzymes which can be used as a nano-medicine for aging and diabetes. The most important finding was the permissible biocompatibility of these BNPs towards brine shrimp larvae and human RBCs, which suggests their environmental and biological safety. This research study gives us insight into the promise of using a green route to synthesize commercially important BNPs with enhanced therapeutic efficacy as compared to conventional treatment options.

Graphical demonstartion of the Manikara zapota-mediated biosynthesis of Bimetallic nanoparticles (BNPs) and evalution of their biological activities.     

Au/Fe3O4 core–shell nanoparticles are an efficient immunochromatography test strip performance enhancer—a comparative study with Au and Fe3O4 nanoparticles

Immunochromatography test strips that use metal particles constructed from Au, Fe₃O₄, and Au/Fe₃O₄ nanoparticles were developed for the rapid detection of avian influenza virus subtype H7 (AIV H7). The principle of this immunochromatography test strip was based on a sandwich immunoreaction in which AIV H7 antigens bind specifically to their corresponding antibodies on a nitrocellulose membrane. An antibody–metal (Au, Fe₃O₄ or Au/Fe₃O₄) nanoparticle conjugate was used as a label and coated onto a glass fiber membrane, which was used as a conjugate pad. To create a test and a control zone, an anti-H7 polyclonal antibody and an anti-IgG antibody were immobilized onto the nitrocellulose membrane, respectively. Positive samples displayed brown/red lines in the test and control zones of the nitrocellulose membrane, whereas negative samples resulted in a brown/red line only in the control zone. The limit of detection (LOD) of the Au/Fe₃O₄ nanoparticle-based immunochromatography test strips was found to be 10^3.5 EID₅₀ (EID₅₀: 50% Egg Infective Dose), which could be visually detected by the naked eye within 15 min. In addition, 200 clinical samples were tested using the Au/Fe₃O₄ nanoparticle-based immunochromatography test strip to estimate its performance, and seven were positive for AIV H7. In summary, the Au/Fe₃O₄ nanoparticle-based immunochromatography test strip offers a simple and cost-effective tool for the rapid detection of AIV H7.

Immunochromatography test strips that use metal particles constructed from Au, Fe₃O₄, and Au/Fe₃O₄ nanoparticles were developed for the rapid detection of avian influenza virus subtype H7 (AIV H7).     

Synthesis and biological characterization of alloyed silver–platinum nanoparticles: from compact core–shell nanoparticles to hollow nanoalloys

Bimetallic nanoparticles consisting of silver and platinum were prepared by a modified seeded-growth process in water in the full composition range in steps of 10 mol%. The particles had diameters between 15–25 nm as determined by disc centrifugal sedimentation (DCS) and transmission electron microscopy (TEM). Whereas particles with high platinum content were mostly spherical with a solid silver core/platinum shell structure, mostly hollow alloyed nanoparticles were observed with increasing silver content. The internal structure and the elemental distribution within the particles were elucidated by high-resolution transmission electron microscopy (HRTEM) in combination with energy-dispersive X-ray spectroscopy (EDX). The particles were cytotoxic for human mesenchymal stem cells (hMSC) above 50 mol% silver. This was explained by dissolution experiments where silver was only released at and above 50 mol% silver. In contrast, platinum-rich particles (less than 50 mol% silver) did not release any silver ions. This indicates that the presence of platinum inhibits the oxidative dissolution of silver.

Bimetallic nanoparticles consisting of silver and platinum were prepared by a modified seeded-growth process in water in the full composition range in steps of 10 mol%.     

Semiconductor ZnO based photosensitizer core–shell upconversion nanoparticle heterojunction for photodynamic therapy

Photodynamic therapy (PDT) as a noninvasive technique is widely used to treat cancer diseases due to its low side effects. PDT based on upconversion nanoparticles (UCNPs) improved tissue penetration and photo-stability. However, traditional photosensitizers and UCNPs were difficult to incorporate, which limited the circulation of the UCNPs in blood and decreased the PDT effect. Herein, we designed NaErF₄@ZnO UCNPs for potential application in thyroid tumor cell PDT. With ZnO coated on NaErF₄, the blue (415 nm), green (525 nm/545 nm) and red (661 nm) upconversion luminescence enhanced compared with that of NaErF₄ core nanoparticles. Particularly, the generation of UV upconversion emission by NaErF₄ sensitized ZnO, which catalyzed H₂O and O₂ to produce ROS reactive oxygen species (ROS) to induce papillary thyroid carcinoma (PTC) cell lines BHP 5-16. With 1000 μg mL⁻¹ of NaErF₄@ZnO UCNPs, the viability of BHP 5-16 cells decreased to about 41% as measured by CCK8 assay with 980 nm NIR irradiation. Moreover, it was confirmed that NaErF₄@ZnO UCNPs had low toxicity for BHP 5-16 cells. All these results indicated that NaErF₄@ZnO upconversion nanoparticles were an excellent platform for PDT treatment.

NaErF₄@ZnO UCNPs for potential application in thyroid tumor cell PDT.     

Chemically activated core–shell structured IF-WS2@C nanoparticles enhance sugarcane-based carbon/epoxy nanocomposites

Ternary composites have demonstrated better capability than binary composites in enhancing the mechanical properties of the modified epoxy resins and are, therefore, currently under intensive investigation. Herein, we report a novel ternary nanocomposite prepared by filling a binary BPF (bisphenol F epoxy resin)/SCPs (sugarcane-based carbon powders) matrix with C-coated inorganic fullerene-like tungsten disulfide (IF-WS₂@C) nanoparticles, and the analysis of its interface synergetic effect using XPS/FTIR. This activated nano-carbon core–shell structure filler is considered an ideal nanofiller and shows the excellent mechanical performance of the ternary composites. XRD, IR, XPS, SEM, and TEM characterizations were applied in investigating this nanocomposite. The improvement of the thermal and mechanical properties demonstrated the enhancement effects of this nanofiller. The results show that the great improvement of the bending modulus of 39.4% increased with the addition of 0.5 wt% IF-WS₂@C nanoparticles, while 34.1% enhancement of bending strength was obtained with the addition of 0.2 wt% IF-WS₂@C nanoparticles. The hardness and thermal conductivity were also boosted up to 5.2% and 33.1% with 0.5 wt% addition, respectively. The incorporation of a chemically activated coating may provide a novel means for improving graphite crystallization, which could somehow expand the potential application of IF-WS₂@C nanoparticles.

Schematic diagram and typical curing mechanism of epoxy resins and the unique interactions of the IF-WS₂@C nanoparticles introduced into the matrix.     

A robust electrochemical immunosensor based on core–shell nanostructured silica-coated silver for cancer (carcinoembryonic-antigen-CEA) diagnosis

This work addresses the fabrication of an efficient, novel, and economically viable immunosensing armamentarium that will detect the carcinoembryonic antigen (CEA) typically associated with solid tumors (sarcomas, carcinomas, and lymphomas) and is used as a clinical tumor marker for all these malignancies. We synthesized silver nanoparticles by single-step chemical reduction and coated with silica using a modified Stober method to fabricate silica-coated silver core–shell nanoparticles. The morphologies, structure, and size of the nanoparticles were characterized by Transmission Electron Microscopy (TEM), UV-Visible spectroscopy, X-ray diffraction (XRD), Raman spectroscopy, Fourier Transform Infra-Red Spectroscopy (FTIR), and Dynamic Light Scattering (DLS), respectively. The results indicated that the average size of Ag nanoparticles and silica-coated Ag nanoparticles is 50 nm and 80 nm, respectively. Our TEM results indicate that the silica-shell uniformly encapsulates silver core particles. Further, a disposable electrochemical immunosensor for carcinoembryonic antigen (CEA) was proposed based on the antigen immobilized in a silica-coated silver core–shell nanoparticle film on the surface of an indium–tin–oxide (ITO) flat substrate. The morphological characteristics of the constructed biosensor were observed by scanning electron microscopy (SEM) and electrochemical methods. Electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) were employed for the characterization of the proposed bioelectrode. The cyclic voltammogram appears to be more irreversible on silica coated silver core–shell nanoparticles. It is found that the fabricated immunosensor shows fast potentiometric response under the optimized conditions. The CEA could be determined in the linear range from 0.5 to 10 ng mL⁻¹ with a detection limit of 0.01 ng mL⁻¹ using the interface. The developed flat substrate of ITO for CEA detection (the model reagent) is a potentially promising immunosensing system, manifests good stability, and allows batch fabrication because of its economic feasibility.

The process flow of disposable electrochemical immunosensor fabrication.     

One-pot one-step synthesis of Au@SiO2 core–shell nanoparticles and their shell-thickness-dependent fluorescent properties

Herein, we report a one-pot one-step method for the preparation of Au@SiO₂ core–shell nanoparticles (NPs) via a facile heating treatment of an alcoholic-aqueous solution of chloroauric acid (HAuCl₄), 2-methylaminoethanol (2-MAE), cetyltrimethylammonimum bromide (CTAB), and tetraethylorthosilicate (TEOS). The size of the Au core and the thickness of the silica shell can be easily controlled by simply adjusting the volume of HAuCl₄ and TEOS, respectively, which can hardly be achieved by other approaches. The as-prepared Au@SiO₂ core–shell NPs exhibited shell-thickness-dependent fluorescent properties. The optimum fluorescence enhancement of fluorescein isothiocyanate (FITC) was found to occur at a silica shell thickness of 34 nm with an enhancement factor of 5.0. This work provides a new approach for the preparation of Au@SiO₂ core–shell NPs and promotes their potential applications in ultrasensitive analyte detection, theranostics, catalysts and thin-film solar cells.

Au@SiO₂ core–shell nanoparticles with tunable Au core size and silica shell thickness were prepared by a facile one-pot one-step method.     

Co(OH)F nanorods@KxMnO2 nanosheet core–shell structured arrays for pseudocapacitor application

In this work, Co(OH)F nanorods@K_xMnO₂ nanosheet core–shell nanostructure was assembled on Ni foam by a facile hydrothermal method and incorporated with an electrodeposition process. Benefiting from their core–shell nanostructure and heterogeneous nanocomposites, the arrays present high areal capacitance up to 1046 mF cm⁻² at 1 mA cm⁻² and display a remarkable specific capacitance retention of 118% after 3000 cycles. When the current density increases to 10 mA cm⁻², the capacitance is 821 mF cm⁻² displaying a good rate capability. The excellent electrochemical properties allow them to be used as a promising electrode material for pseudocapacitors and display wide application potential in the field of electrochemical capacitors.

In this work, Co(OH)F nanorods@K_xMnO₂ nanosheet core–shell nanostructure was assembled on Ni foam by a facile hydrothermal method and incorporated with an electrodeposition process.     

Catalytically active and thermally stable core–shell gold–silica nanorods for CO oxidation

Deactivation based on sintering phenomena is one of the most costly issues for the industrial application of metal nanoparticle catalysts. To address this drawback, mesoporous silica encapsulation is reported as a promising strategy to stabilize metallic nanoparticles towards use in high temperature catalytic applications. These protective shells provide significant structural support to the nanoparticles, while the mesoporosity allows for efficient transport of the reactants to the catalytically active surface of the metallic nanoparticle in the core. Here, we extend the use of gold nanorods with mesoporous silica shells by investigating their stability in the CO oxidation reaction as an example of high temperature gas phase catalysis. Gold nanorods were chosen as the model system due to the availability of a simple, high yield synthesis method for both the metallic nanorods and the mesoporous silica shells. We demonstrate the catalytic activity of gold nanorods with mesoporous silica shells at temperatures up to 350 °C over several cycles, as well as the thermal stability up to 500 °C, and compare these results to surfactant-stabilized gold nanorods of similar size, which degrade, and lose most of their catalytic activity, before reaching 150 °C. These results show that the gold nanorods protected by the mesoporous silica shells have a significantly higher thermal stability than surfactant-stabilized gold nanorods and that the mesoporous silica shell allows for stable catalytic activity with little degradation at high temperatures.

Gold nanorods stabilized with mesoporous silica shells are characterized and used as the catalyst for a model CO oxidation reaction to counter the costly sintering phenomena found in many industrial nanoparticle catalysts.     

Double-exponential refractive index sensitivity of metal–semiconductor core–shell nanoparticles: the effects of dual-plasmon resonances and red-shift

In order to improve the refractive index sensitivity of a localized surface plasmon resonance (LSPR) sensor, we present a new type of LSPR sensor whose refractive index sensitivity can be improved by greatly increasing the plasmon wavelength red-shift of metal–semiconductor core–shell nanoparticles (CSNs). Using extended Mie theory and Au@Cu_2−xS CSNs, we theoretically investigate the optical properties of metal–semiconductor CSNs in the entire near-infrared band. Compared with dielectric–metal and metal–metal CSNs under the same conditions, the metal–semiconductor CSNs have a higher double-exponential sensitivity curve because their core and shell respectively support two LSPRs that greatly increase the LSPR red-shift to the entire near-infrared range. It is worth noting that the sensitivity can be improved effectively by increasing the ratio of the shell-thickness to core-radius, instead of decreasing it in the case of the dielectric–metal CSNs. The underlying reason for the enhancement of sensitivity is the increase of repulsive force with the enlargement of shell thickness, which is different from the dielectric–metal CSNs. This design method not only paves the way for utilizing metal–semiconductor CSNs in biology and chemistry, but also proposes new ideas for the design of sensors with high sensitivity.

We present a new type of localized surface plasmon resonance (LSPR) sensor whose refractive index sensitivity can be improved by greatly increasing the plasmon wavelength red-shift of metal–semiconductor core–shell nanoparticles (CSNs).     

Homo–hetero/core–shell structure design strategy of NaYF4 nanocrystals for superior upconversion luminescence

A comprehensive strategy has been developed to construct nano-sized homogeneous and heterogeneous core/shell structures of NaYF₄ host. Synthesis conditions of cubic phase/α-NaYF₄ and hexagonal phase/β-NaYF₄ are discussed. Pure cubic NaYF₄:Yb,Er nanocrystals were synthesized with different average sizes extending from 7 nm to 15 nm by varying the reaction time. Temperature and time thresholds of hexagonal nucleation were determined and utilized for controlled core/shell structures of different phases. α-NaYF₄:Yb,Er@α-NaYF₄, α-NaYF₄:Yb,Er@β-NaYF₄, β-NaYF₄:Yb,Er@α-NaYF₄, and β-NaYF₄:Yb,Er@β-NaYF₄ core/shell structures were prepared by adopting the required conditions to achieve the desired phase. Excess sodium was used to grow hexagonal shell over metastable cubic core under controlled conditions of reaction time and temperature to prevent the structural transition of the core. Upconversion emission spectra have also been obtained. UCL integrated intensities demonstrated about 5-fold enhancement for α-shell over α-core as compared to the core alone and 22-fold enhancement with β-shell. On the other hand, α-shell over β-core exhibited 5-fold enhancement and β-shell over β-core exhibited 6-fold enhancement.

Establishment of essential conditions of different phases of NaYF₄ and their utilization for the synthesis of core/shell structures to achieve the enhancement of UCL intensities.     

The structural transition of bimetallic Ag–Au from core/shell to alloy and SERS application

It is well-known that Ag–Au bimetallic nanoplates have attracted significant research interest due to their unique plasmonic properties and surface-enhanced Raman scattering (SERS). In recent years, there have been many studies on the fabrication of bimetallic nanostructures. However, controlling the shape, size, and structure of bimetallic nanostructures still has many challenges. In this work, we present the results of the synthesis of silver nanoplates (Ag NPls), and Ag–Au bimetallic core/shell and alloy nanostructures, using seed-mediated growth under green LED excitation and a gold salt (HAuCl₄) as a precursor of gold. The results show that the optical properties and crystal structure strongly depend on the amount of added gold salt. Interestingly, when the amount of gold(x) in the sample was less than 0.6 μmol (x < 0.6 μmol), the structural nature of Ag–Au was core/shell, in contrast x > 0.6 μmol gave the alloy structure. The morphology of the obtained nanostructures was investigated using the field emission scanning electron microscopy (FESEM) technique. The UV–Vis extinction spectra of Ag–Au nanostructures showed localized surface plasmon resonance (LSPR) bands in the spectral range of 402–627 nm which changed from two peaks to one peak as the amount of gold increased. Ag–Au core/shell and alloy nanostructures were utilized as surface enhanced Raman scattering (SERS) substrates to detect methylene blue (MB) (10⁻⁷ M concentration). Our experimental observations indicated that the highest enhancement factor (EF) of about 1.2 × 10⁷ was obtained with Ag–Au alloy. Our detailed investigations revealed that the Ag–Au alloy exhibited significant EF compared to pure metal Ag and Ag–Au core/shell nanostructures. Moreover, the analysis of the data revealed a linear dependence between the logarithm of concentration (log C) and the logarithm of SERS signal intensity (log I) in the range of 10⁻⁷–10⁻⁴ M with a correlation coefficient (R²) of 0.994. This research helps us understand better the SERS mechanism and the application of Raman spectroscopy on a bimetallic surface.

It is well-known that Ag–Au bimetallic nanoplates have attracted significant research interest due to their unique plasmonic properties and surface-enhanced Raman scattering (SERS).     

Facile fabrication and low-temperature bonding of Cu@Sn–Bi core–shell particles for conductive pastes

The rapid development of flexible wearable electronics arouses huge demand for low-temperature sintering metal inks applied to temperature-sensitive substrates. The high sintering temperature and easy oxidation limited the application of Cu-based pastes. A two-step method involving liquid co-reduction and heat ripening was developed to synthesize Cu@Sn–Bi core–shell particles. The thickness of Sn–Bi shells can be flexibly adjusted via changing the mass ratio of Cu to Sn–Bi. The volume resistivity of printed circuits using Cu@Sn–Bi pastes solidified at 200 °C was as low as 481 μΩ cm, which increased by 11.8% after an aging process at 190 °C for 6 h. The outstanding stability in a harsh environment would attribute to the effective protection of Sn–Bi alloy shells. This work suggests a new pathway toward the low-temperature bonding and anti-oxidation of Cu particles as conductive fillers, which can be widely applied to the additive manufacturing of flexible wearable electronics.

Cu@Sn–Bi core–shell particles were synthesized and used as conductive fillers of ink applied to flexible printed circuits. This work provides new insights into the low-temperature bonding and anti-oxidation protection of Cu-based conductive pastes.