Preparation of open-porous stereocomplex PLA/PBAT scaffolds and correlation between their morphology,mechanical behavior,and cell compatibility

For tissue engineering applications, it is essential that biodegradable scaffolds have accessible mechanical properties, high porosity, and good biocompatibility to support the formation of new tissues. In this study, we have prepared stereocomplex polylactide (sc-PLA) incorporated poly(butylene adipate-co-terephthalate) (PBAT) scaffolds by non-solvent induced phase separation (NIPS). Also, we have characterized and compared the morphology, thermal, mechanical, and wettability properties as well as preliminary biocompatibility of scaffolds. The developed sc-PLA/PBAT scaffolds possess high porosity (>94%), well-connected open microporous structures, accessible mechanical properties, and excellent water permeability. As the content of PBAT increased, the average diameter of the sc-PLA/PBAT scaffolds decreased while the mechanical properties improved. The tensile strength was improved to 3.8 MPa while the neat PLA scaffold was 0.3 MPa, and the elongation of the scaffold was six times higher than neat PLA scaffold. Fibroblasts cells seeded on the structure maintained phenotypic shape, and the developed scaffold structure was observed to be highly capable of supporting the cell attachment and proliferation.

For tissue engineering applications, it is essential that biodegradable scaffolds have accessible mechanical properties, high porosity, and good biocompatibility to support the formation of new tissues.     

Crystallization,thermal and mechanical properties of stereocomplexed poly(lactide) with flexible PLLA/PCL multiblock copolymer

In this work, the synthesized PLLA/PCL multi-block copolymers with different compositions were introduced into a stereocomplexed poly(lactide) (sc-PLA) matrix to accelerate the stereocomplexation of PLA enantiomers and improve its inherent brittleness. The PLLA/PCL multi-block copolymers were in different compositions to adjust the molecular weight of the PLLA block. The structure, molecular weight, crystallization behavior, crystal structure and thermal stability of PLLA/PCL multi-block copolymers were investigated. The results indicated that PLLA/PCL multi-block copolymers with controllable structure and composition were successfully synthesized. On this basis, the blends of sc-PLA and PLLA/PCL multi-block copolymers were prepared by solution casting, and characterized. The results revealed that the introduction of PLLA/PCL multi-block copolymers promoted the stereocomplexation of the PLA enantiomers during the melting crystallization process to obtain a complete stereocomplexed material. But the presence of the PCL block leads to a decrease in the melting temperature of the stereocomplex and difficulty in homogeneous nucleation. Compared with sc-PLA, the elongation at break of the blends was significantly improved and their tensile strengths were only slightly reduced. And the thermal stability and mechanical properties of the blends could be adjusted by controlling the content and composition of PCL/PLLA multi-block copolymers. These results revealed that the degree of stereocomplexation and toughness of sc-PLA were improved, which may expand the application fields of PLA-based materials.

The PLLA/PCL multi-block copolymer was introduced into the stereocomplexed PLA matrix, and its effect on the crystallization, thermal and mechanical properties of the stereocomplexed PLA was discussed.     

Blends of poly(butylene adipate-co-terephthalate) (PBAT) and stereocomplex polylactide with improved rheological and mechanical properties

Biodegradable blends of poly(butylene adipate-co-terephthalate) (PBAT) and stereocomplex polylactide (sc-PLA) were prepared herein via a melt blending method at various sc-PLA loadings. Wide-angle X-ray diffraction and differential scanning calorimetry results verified that complete stereocomplex polylactide crystallites in the PBAT could be achieved. Scanning electron microscopy observation indicated that sc-PLA was dispersed in the PBAT matrix as spherical particles; the dispersed size of the sc-PLA did not display a pronounced increase once the content of sc-crystallites reached a critical gel point. As solid fillers, sc-PLA could reinforce the PBAT matrix in a relatively wider temperature region and accelerate the non-isothermal crystallization of PBAT. The properties of PBAT were greatly improved after blending with sc-PLA, particularly when a percolation network structure of spherical filler had formed in the blends. In addition, all the blends showed higher yield stresses and moduli than those of the neat PBAT but exhibited reduction in elongations in tensile mechanical tests. These results would be interesting to the industrial polymer materials community, and may be of significant use and importance for the wider practical application of PBAT.

Schematic representation of formed solid sc-PLA in the PBAT melting during melt processing.     

High-sensitivity refractive index of Au@Cu2−xS core–shell nanorods

A high refractive index sensitivity of Au@Cu_2−xS core–shell nanorods working in the near-infrared is theoretically demonstrated. The sensitivity of our sensor reaches 1200 nm per Refractive Index Unit (RIU), which is higher than that of other metal–metal core–shell nanorods. The reason is that the new materials and structure of Au@Cu_2−xS core–shell nanorods lead to a unique sensing principle. It is noteworthy that the refractive index (RI) sensitivity is more susceptible to the effects of the shell-thickness to core-radius ratio than to the aspect ratio. These results show that the excellent sensitivity performance of Au@Cu_2−xS core–shell nanorods working in the near-infrared can be treated as a new tool to detect the minute variations in refractive index for small amounts of chemicals and biomolecules.

A high refractive index sensitivity of Au@Cu_2−xS core–shell nanorods working in the near-infrared is theoretically demonstrated.     

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.     

Preparation of MoS2-based polydopamine-modified core–shell nanocomposites with elevated adsorption performances

New molybdenum disulfide (MoS₂)-based core–shell nanocomposite materials were successfully prepared through the self-assembly of mussel-inspired chemistry. Characterization by Fourier transform infrared, thermogravimetric analysis, scanning electron microscope and transmission electron microscopy revealed that the surface of the flaked MoS₂ was homogeneously coated with a thin layer of polydopamine (PDA). Dye adsorption performances of the synthesized MoS₂–PDA nanocomposites were investigated at different pH values and reaction times. Compared with pure MoS₂ nanosheets, the obtained core–shell nanocomposites showed elevated adsorption performances and high stability, indicating their potential applications in wastewater treatment and composite materials.

New core–shell MoS₂–PDA nanocomposites are prepared via mussel-inspired chemistry and a simple interfacial self-assembly process, demonstrating potential applications in wastewater treatment and self-assembled core–shell composite materials.     

A core–shell structured polyacrylonitrile@poly(vinylidene fluoride-hexafluoro propylene) microfiber complex membrane as a separator by co-axial electrospinning

A novel and facile core–shell structured polyacrylonitrile@poly (vinylidene fluoride-hexafluoro propylene) (PAN@PVDF-HFP) microfiber complex membrane was designed and fabricated via co-axial electrospinning, which was used as a separator in lithium-ion batteries. Poly(vinylidene fluoride-co-hexafluoro propene) (PVDF-HFP) and polyacrylonitrile (PAN) were used as the shell (outer) layer and core (inner), respectively. Structure, surface morphology, porosity, and thermal properties of the core–shell structured microfiber membranes were investigated. Compared with the traditional commercial porous polyethylene (PE) separator, the PAN@PVDF-HFP microfiber complex membranes exhibited higher porosity, superior thermal stability, better electrolyte wettability and higher ionic conductivity. As a consequence, batteries assembled with the PAN@PVDF-HFP microfiber complex membrane display better cycling stability and superior rate performance compared to those with the PE separator.

A novel and facile core–shell structured polyacrylonitrile@poly (vinylidene fluoride-hexafluoro propylene) (PAN@PVDF-HFP) microfiber complex membrane was designed and fabricated via co-axial electrospinning.     

Core–shell fibremats comprising a poly(AM/DAAM)/ADH nanofibre core and nylon6 shell layer are an attractive immobilization platform for constructing immobilised enzymes

Core–shell fibremats, comprising poly(acrylamide)-co-poly(diacetone–acrylamide)/adipic dihydrazide [poly(AM/DAAM)/ADH] core-nanofibres and hydrophobic polymer shell layers, are a new class of platforms for constructing various immobilised enzymes. In this study, to elucidate the impacts of the shell-layer material on fibremat properties and enzymatic activities, we synthesised core–shell fibremats with shell layers comprising nylon6 or acetyl cellulose (AcCel) instead of poly(ε-caprolactone) (PCL), as in our previous study. Transmission and scanning electron microscopy images revealed that the lactase-encapsulated poly(AM/DAAM)/ADH-nylon6 and -AcCel fibremats were both constructed like the poly(AM/DAAM)/ADH-PCL one. Leakage measurements of the beforehand loaded molecules inside the core-nanofibres revealed that both fibremats exhibited efficient permeability for low-molecular-weight molecules and stable retention of enzyme molecules inside the core-nanofibres. Meanwhile, the fibremats'' mechanical properties considerably depended on the choice of shell-layer material. The thermal analyses of the lactase-encapsulated fibremats revealed residual water inside the core nanofibres. The core–shell fibremats fabricated with a nylon6 or PCL shell exhibited excellent enzymatic activities (102 and 114%, respectively, compared to that of free lactase), superior to that of the same amount of free enzyme in a buffer. Furthermore, both core–shell fibremats retained over 95% of their initial enzymatic activities, even after they were re-used 10 times.

Core–shell fibremats, comprising poly(AM/DAAM)/ADH core-nanofibres and hydrophobic shell layers, are a new class of attractive platform for constructing various immobilised enzymes.     

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.     

Counterion coupled (COCO) gemini surfactant capped Ag/Au alloy and Ag@Au core–shell nanoparticles for cancer therapy

Hybrid silver (Ag)–gold (Au) nanoparticles (NPs) with different sizes and compositions were synthesized. Ag/Au alloy and Ag@Au core–shell type NPs were prepared from Ag and Au with various ratios using the COCO gemini surfactant, 1,6-bis (N,N-hexadecyldimethylammonium) adipate (COCOGS), 16-6-16 as a stabilizer. The formation of the Ag/Au alloy and Ag@Au core–shell was confirmed by UV-visible absorption spectroscopy, high-resolution transmission electron microscopy (HRTEM), energy-dispersive X-ray spectroscopy (EDX) and selected area electron diffraction (SAED) patterns. Depending on the composition of the Ag/Au alloy NPs, the λ_max values varied from 408 nm to 525 nm. FTIR measurements were used to evaluate the adsorption of the COCO gemini surfactant (16-6-16) on the Ag/Au alloy and Ag@Au core–shell surface. In this present work, we study how to achieve the stability and activity of the COCO gemini surfactant (16-6-16) capped Ag/Au alloy and Ag@Au core–shell NPs for developing novel anti-cancer agents by evaluating their potentials in the Hep-2 cell line model. Thus the developed core–shell NPs were possibly involved in inducing cytotoxicity followed by inhibition of cell proliferation to the cancer cells with apoptosis induction. The developed core–shell NPs might serve as highly applicable agents in the development of next-generation cancer chemotherapeutic agents.

In this work hybrid silver (Ag)–gold (Au) nanoparticles (NPs) with different sizes and compositions were synthesized and applied for anticancer evaluations and which is effectively involved in cancer cell apoptosis through DNA damage.     

In situ synthesis of copper nanoparticles encapsulated by nitrogen-doped graphene at room temperature via solution plasma

Metal–carbon core–shell nanostructures have gained research interest due to their better performances in not only stability but also other properties, such as catalytic, optical, and electrical properties. However, they are limited by complicated synthesis approaches. Therefore, the development of a simple method for the synthesis of metal–carbon core–shell nanostructures is of great significance. In this work, a novel Cu–core encapsulated by a N-doped few-layer graphene shell was successfully synthesized in a one-pot in-liquid plasma discharge, so-called solution plasma (SP), to our knowledge for the first time. The synthesis was conducted at room temperature and atmospheric pressure by using a pair of copper electrodes submerged in a DMF solution as the precursor. The core–shell structure of the obtained products was confirmed by HR-TEM, while further insight information was explained from the results of XRD, Raman, and XPS measurements. The obtained Cu-core encapsulated by the N-doped few-layer graphene shell demonstrated relatively high stability in acid media, compared to the commercial bare Cu particles. Moreover, the stability was found to depend on the thickness of the N-doped few-layer graphene shell which can be tuned by adjusting the SP operating conditions.

An excellent corrosion protection for copper nanoparticles by nitrogen-doped few-layer graphene via solution plasma process.     

Photocatalytic hydrogen production and storage in carbon nanotubes: a first-principles study

As it is a promising clean energy source, the production and storage of hydrogen are crucial techniques. Here, based on first-principles calculations, we proposed an integral strategy for the production and storage of hydrogen in carbon nanotubes via photocatalytic processes. We considered a core–shell structure formed by placing a carbon nitride nanowire inside a carbon nanotube to achieve this goal. Photo-generated holes on the carbon nanotube surface promote water splitting. Driven by intrinsic electrostatic field in the core–shell structures, protons produced by water splitting penetrate the carbon nanotube and react with photo-generated electrons on the carbon nitride nanowire to produce hydrogen molecules in the carbon nanotube. Because carbon nanotubes have high hydrogen storage capacity, this core–shell structure can serve as a candidate system for photocatalytic water splitting and safe hydrogen storage.

The production and storage of hydrogen in CNNW/CNT core–shell structures via photocatalytic processes.     

Controllable synthesis of AgNWs@PDA@AgNPs core–shell nanocobs based on a mussel-inspired polydopamine for highly sensitive SERS detection

In this work, a series of AgNWs@PDA@AgNPs core–shell nanocobs based on a mussel-inspired polydopamine (PDA) were controllably synthesized and achieve highly sensitive SERS detection. Owing to the existence of abundant catechol and amine functional groups, PDA molecules could assemble a functional layer on the surface of silver nanowires (AgNWs) and exhibit exceptional adhesion performance. More importantly, silver nanoparticles (AgNPs) with controlled coverage and size were achieved on the surface of the PDA layer by in situ reduction of silver ions into AgNPs with catechol functional groups, forming AgNWs@PDA@AgNPs core–shell nanocobs. By regulating synergistical effect between the AgNWs and AgNPs, the AgNWs@PDA@AgNPs core–shell nanocobs demonstrated a highly sensitive and stable SERS response to Rhodamine 6G (R6G) molecules, and a low limit of detection down to 10⁻¹² M. Furthermore, the AgNWs@PDA@AgNPs core–shell nanocobs showed an excellent reproducibility and superior stability as a SERS substrate to achieve trace detection. This strategy would have great potential to fabricate multifarious SERS-active substrates that make it possible to detect single molecules and singles cell in chemical and biological fields.

An effective strategy was developed to controllably synthesize a series of AgNWs@PDA@AgNP core–shell nanocobs based on a mussel-inspired polydopamine and achieve highly sensitive SERS detection.     

Magnetic–plasmonic Ni@Au core–shell nanoparticle arrays and their SERS properties

In this paper, large-area magnetic–plasmonic Ni@Au core–shell nanoparticle arrays (NPAs) with tunable compositions were successfully fabricated by a direct laser interference ablation (DLIA) incorporated with thermal dewetting method. The magnetic properties of the Ni@Au core–shell NPAs were analyzed and the saturation magnetization (M_s) of the Ni₈₀@Au₂₀ nanoparticles was found to be higher than that of nickel-only nanoparticles with the same diameter. Using Rhodamine 6G (R6G) as a Raman reporter molecule, the surface enhanced Raman scattering (SERS) property of the Ni@Au core–shell NPAs with a grain size distribution of 48 ± 42 nm and a short-distance order of about 200 nm was examined. A SERS enhancement factor of 2.5 × 10⁶ was realized on the Ni₅₀@Au₅₀ NPA substrate, which was 9 times higher than that for Au nanoparticles with the same size distribution. This was due to the enhanced local surface plasmon resonance (LSPR) between the ferromagnetic Ni cores and the surface polariton of the Au shells of each nanoparticle. The fabrication of the Ni@Au core–shell NPAs with different compositions offers a new avenue to tailor the optical and magnetic properties of the nanostructured films for chemical and diagnostic applications.

In this paper, large-area magnetic–plasmonic Ni@Au core–shell nanoparticle arrays (NPAs) with tunable compositions were successfully fabricated by a direct laser interference ablation (DLIA) incorporated with thermal dewetting method.     

Core–shell Pd–P@Pt–Ni nanoparticles with enhanced activity and durability as anode electrocatalyst for methanol oxidation reaction

Pd–P@Pt–Ni core–shell nanoparticles, which consisted of a Pd–P alloy as a core and Pt–Ni thin layer as a shell, were explored as electrocatalysts for methanol oxidation reaction. The crystallographic information and the electronic properties were fully investigated by X-ray diffraction and X-ray photoelectron spectroscopy. In the methanol electrooxidation reaction, the particles showed high catalytic activity and strong resistance to the poisoning carbonaceous species in comparison with those of commercial Pt/C and the as-prepared Pt/C catalysts. The excellent durability was demonstrated by electrochemically active surface area loss and chronoamperometric measurements. These results would be due to the enhanced catalytic properties of Pt by the double synergistic effects from the core part and the nickel species in the shell part.

The Pd–P@Pt–Ni core–shell nanoparticles consist of an amorphous core and a low-crystalline shell. They exhibit the excellent catalytic properties in MOR owing to the double synergistic effects from the core and the nickel species in the shell.     

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.     

Enhanced oxygen reduction activity of Pt shells on PdCu truncated octahedra with different compositions

Pd@Pt core–shell nanocrystals with ultrathin Pt layers have received great attention as active and low Pt loading catalysts for oxygen reduction reaction (ORR). However, the reduction of Pd loading without compromising the catalytic performance is also highly desired since Pd is an expensive and scarce noble-metal. Here we report the epitaxial growth of ultrathin Pt shells on Pd_xCu truncated octahedra by a seed-mediated approach. The Pd/Cu atomic ratio (x) of the truncated octahedral seeds was tuned from 2, 1 to 0.5 by varying the feeding molar ratio of Pd to Cu precursors. When used as catalysts for ORR, these three Pd_xCu@Pt core–shell truncated octahedra exhibited substantially enhanced catalytic activities compared to commercial Pt/C. Specifically, Pd₂Cu@Pt catalysts achieved the highest area-specific activity (0.46 mA cm⁻²) and mass activity (0.59 mA μg_Pt⁻¹) at 0.9 V, which were 2.7 and 4.5 times higher than those of the commercial Pt/C. In addition, these Pd_xCu@Pt core–shell catalysts showed a similar durability with the commercial Pt/C after 10 000 cycles due to the dissolution of active Cu and Pd in the cores.

Pd_xCu@Pt core–shell truncated octahedra were synthesized and exhibited substantially enhanced catalytic properties for oxygen reduction reaction relative to Pt/C.     

SiO2@MnOx@Na2WO4@SiO2 core–shell-derived catalyst for oxidative coupling of methane

SiO₂@MnO_x@Na₂WO₄@SiO₂ core–shell catalysts were prepared and their fabrication was confirmed using transmission electron microscopy. The formation of Mn-based nanosheets on the silica spheres is important for the deposition of nanoscopic Na₂WO₄. The SiO₂@MnO_x@Na₂WO₄@SiO₂ core–shell catalysts were used for the oxidative coupling of methane at a temperature of 700–800 °C at which the nanostructures were completely destroyed. Although the core–shell structures did not survive the high-temperature oxidative coupling of methane, the selective production of olefins and paraffins can be attributed to highly dispersed Na₂WO₄ derived from confined core–shell structures.

SiO₂@MnO_x@Na₂WO₄@SiO₂ core–shell catalysts were prepared for the oxidative coupling of methane.     

Facilely controlled synthesis of a core-shell structured MOF composite and its derived N-doped hierarchical porous carbon for CO2 adsorption

A new strategy for controlled synthesis of a MOF composite with a core–shell structure, ZIF-8@resorcinol–urea–formaldehyde resin (ZIF@RUF), is reported for the first time through in situ growth of RUF on the surface of ZIF-8 nanoparticles via an organic–organic self-assembly process by using hexamethylenetetramine as a formaldehyde-releasing source to effectively control the formation rate of RUF, providing the best opportunity for RUF to selectively grow around the nucleation seeds ZIF-8. Compared with the widely reported method for MOF composite synthesis, our strategy not only avoids the difficulty of incorporating MOF crystals into small pore sized materials because of pore limitation, but also effectively guarantees the formation of a MOF composite with a MOF as the core. After carbonization, a morphology-retaining N-doped hierarchical porous carbon characterized by its highly developed microporosity in conjunction with ordered mesoporosity was obtained. Thanks to this unique microporous core–mesoporous shell structure and significantly enhanced porosity, simultaneous improvements of CO₂ adsorption capacity and kinetics were achieved. This strategy not only paves a way to the design of other core–shell structured MOF composites, but also provides a promising method to prepare capacity- and kinetics-increased carbon materials for CO₂ capture.

New strategy for controlled synthesis of core–shell structured ZIF-8 composite and hierarchical N-doped carbon via an effective in situ self-assembly process.     

Understanding metal-enhanced fluorescence and structural properties in Au@Ag core–shell nanocubes

Au@Ag core–shell structures have received particular interest due to their localized surface plasmon resonance properties and great potential as oxygen reduction reaction catalysts and building blocks for self-assembly. In this study, Au@Ag core–shell nanocubes (Au@AgNCs) were fabricated in a facile manner via stepwise Ag reduction on Au nanoparticles (AuNPs). The size of the Au@AgNCs and their optical properties can be simply modulated by changing the Ag shell thickness. Structural characterization has been carried out by TEM, SAED, and XRD. The metal-induced fluorescence properties of probe molecules near the Au@AgNCs were measured during sedimentation of the Au@AgNCs. The unique ring-like building block of Au@AgNCs has dual optical functions as a fluorescence quencher or fluorescence enhancement medium depending on the assembled regions.

The unique ring-like building block of Au@AgNCs has dual optical functions as a fluorescence quencher and fluorescence enhancement medium.