Multishell Silver Indium Selenide-Based Quantum Dots and Their Poly(methyl methacrylate) Composites for Application in Red-Light-Emitting Diodes.

In this work, the production of novel multishell silver indium selenide quantum dots (QDs) shelled with zinc selenide and zinc sulfide through a multistep synthesis precisely designed to develop high-quality red-emitting QDs is explored. The formation of the multishell nanoheterostructure significantly improves the photoluminescence quantum yield of the nanocrystals from 3% observed for the silver indium selenide core to 27 and 46% after the deposition of the zinc selenide and zinc sulfide layers, respectively. Moreover, the incorporation of the multishelled QDs in a poly(methyl methacrylate) (PMMA) matrix via in situ radical polymerization is investigated, and the role of thiol ligand passivation is proven to be fundamental for the stabilization of the QDs during the polymerization step, preventing their decomposition and the relative luminescence quenching. In particular, the role of interface chemistry is investigated by considering both surface passivation by inorganic zinc chalcogenide layers, which allows us to improve the optical properties, and organic thiol ligand passivation, which is fundamental to ensuring the chemical stability of the nanocrystals during in situ radical polymerization. In this way, it is possible to produce silver-indium selenide QD-PMMA composites that exhibit bright red luminescence and high transparency, making them promising for potential applications in photonics. Finally, it is demonstrated that the new silver indium selenide QD-PMMA composites can serve as an efficient color conversion layer for the production of red light-emitting diodes.

Boron Nitride Nanosheet-Magnetic Nanoparticle Composites for Water Remediation Applications.

The combination of 0D nanoparticles with 2D nanomaterials has attracted a lot of attention over the last years due to the unique multimodal properties of resulting 0D-2D nanocomposites. In this work, we developed boron nitride nanosheets (BNNS) functionalized with manganese ferrite magnetic nanoparticles (MNPs). The functionalization process involved attachment of MNPs to exfoliated BNNS by refluxing the precursor materials in a polyol medium. Characterization of the produced BNNS-MNP composites was carried out using powder X-ray diffraction, transmission electron microscopy, vibrating sample magnetometry, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy. The adhesion of MnFe2O4 magnetic nanoparticles onto the BNNS remained unaffected by repeated sonication and heating in a furnace at 400 °C, underscoring the robust nature of the formed bond. FTIR spectra and XPS deconvolution confirmed the presence of strong bonding between BNNS and the MNPs. Membranes were fabricated from the BNNS and the BNNS-MnFe2O4 nanocomposites for evaluating their efficiency in removing the methylene blue dye pollutant. The membranes have been characterized by scanning electron microscopy, Brunauer-Emmett-Teller surface area analysis, and mercury intrusion porosimetry. The effectiveness of dye removal was monitored using ultraviolet-visible spectroscopy. The BNNS-MnFe2O4 nanocomposite membranes exhibited enhanced MB capture compared to membranes made from pure BNNS alone. The recyclability assessment of BNNS-MnFe2O4 demonstrated exceptional performance, retaining 92% efficiency even after eight cycles. These results clearly demonstrate the high potential of these magnetic nanocomposites as reusable materials for water filtration membranes. Furthermore, the introduction of magnetic functionality as part of the membrane brings an exciting opportunity for in situ magnetic heating of the membrane, which shall be explored in future work.

Boron Nitride Nanosheets Functionalized with Fe3O4 and CoFe2O4 Magnetic Nanoparticles for Nanofiltration Applications.

Nanofiltration (NF) is one of the emerging technologies that is very promising for water purification among many other applications. 2D boron nitride (BN) based nanomaterials are excellent building blocks for NF membranes. In our work, BN nanosheets (BNNS) have been functionalized with magnetic nanoparticles (MNPs) to form BNNS-MNP nanocomposites. It was found that the nanocomposites are stable with the MNPs giving very good coverage with both magnetite and cobalt ferrite MNPs and showing good attachment and stability to sonication. These nanocomposites have been tested for removal of methylene blue (MB) dye and MNPs from water. BNNS-magnetite nanocomposites showed higher removal efficiency of the MB from water than the corresponding pure BNNS, while the BNNS-cobalt ferrite removal efficiency was slightly less than the pure BNNS. The BNNS-cobalt ferrite material was regenerated by burning off the MB and recycled to show the recyclability of this material. The BNNS membranes were tested for filtration of 14 ± 4 nm magnetite MNPs and were found to capture 100% of the nanoparticles with no MNPs left in the filtrate. Thus, we have developed magnetic nanocomposite membranes, which have demonstrated great potential for water remediation. We believe that this research opens up promising ways for production of 2D nanocomposite materials with multiple applications.

MnFe2O4@SiO2@CeO2 core-shell nanostructures for applications in water remediation.

Removal of dye pollutants from wastewater is among the most important emerging needs in environmental science and engineering. The main objective of our work is to develop new magnetic core-shell nanostructures and explore their use for potential removal of pollutants from water using an external magnetic field. Herein, we have prepared magnetic core-shell nanoparticles that demonstrated excellent dye pollutant adsorbent properties. These nanoparticles are composed of a manganese ferrite magnetic core coated with silica, to protect the core and enable further functionalisation, then finally coated with ceria, which is shown to be an effective adsorbent. The magnetic core-shell nanostructures have been synthesized by a modification of solvothermal synthesis. The nanoparticles were fully characterised at each stage of the synthesis by powder X-ray diffraction (pXRD), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM) and Fourier transform infrared spectroscopy (FTIR). These particles were found to be effective in removing methylene blue (MB) dye from water, which was validated by UV-visible (UV-vis) spectroscopy. These particles can be quickly removed from solution using a permanent magnet and then can be recycled after being placed in the furnace at 400 °C to burn off any organic residues. The particles were found to retain their ability to adsorb the pollutant after several cycles and TEM images of the particles after several cycles showed no change in the morphology. This research demonstrated the capacity of magnetic core-shell nanostructures to be used for water remediation.

XRD and Spectroscopic Investigations of ZIF-Microchannel Glass Plates Composites.

In this study, new composite materials comprising zeolitic imidazolate framework (ZIF) structures and microchannel glass (MCG) plates were fabricated using the hydrothermal method and their morphological and spectral properties were investigated using XRD, SEM, FTIR, and Raman spectroscopy. XRD studies of powder samples revealed the presence of an additional phase for a ZIF-8 sample, whereas ZIF-67 samples, which were prepared through two different chemical routes, showed no additional phases. A detailed analysis of the FTIR and micro-Raman spectra of the composite samples revealed the formation of stable ZIF structures inside the macropores of the MCG substrate. The hydrophilic nature of the MCG substrate and its interaction with the ZIF structure resulted in the formation of stable ZIF-MCG composites. We believe that these composite materials may find a wide range of important applications in the field of sensors, molecular sieving.

Design and Development of Magnetic Iron Core Gold Nanoparticle-Based Fluorescent Multiplex Assay to Detect Salmonella.

Salmonella is a bacterial pathogen which is one of the leading causes of severe illnesses in humans. The current study involved the design and development of two methods, respectively using iron oxide nanoparticle (IONP) and iron core gold nanoparticle (ICGNP), conjugated with the Salmonella antibody and the fluorophore, 4-Methylumbelliferyl Caprylate (4-MUCAP), used as an indicator, for its selective and sensitive detection in contaminated food products. Twenty double-blind beverage samples, spiked with Salmonella enteritidis, Staphylococcus aureus, and Escherichia coli, were prepared in sterile Eppendorf® tubes at room temperature. The gold layer and spikes of ICGNPs increased the surface areas. The ratio of the surface area is 0.76 (IONPs/ICGNPs). The comparative sensitivity and specificity of the IONP-based and the ICGNP-based methods to detect Salmonella were determined. The ICGNP method shows the limit of detection is 32 Salmonella per mL. The ICGNPs had an 83.3% sensitivity and a 92.9% specificity value for the presence and detection of Salmonella. The IONP method resulted in a limit of detection of 150 Salmonella per mL, and a 66.7% sensitivity and 83.3% specificity for the presence and detection of Salmonella. The higher surface area of ICGNPs increases the efficiency of detection. The monitoring of Salmonella can thus be achieved by a rapid magnetic fluorescent assay using a smartphone for image capture and analyze, providing quantitative results. The findings from the present study would help to detect Salmonella rapidly in water. It can improve the microbial quality of water and food safety due to the presence of Salmonella in the water environment.

Correction: Electrostatically modulated magnetophoretic transport of functionalised iron-oxide nanoparticles through hydrated networks.

Correction for 'Electrostatically modulated magnetophoretic transport of functionalised iron-oxide nanoparticles through hydrated networks' by Stephen Lyons et al., Nanoscale, 2020, 12, 10550-10558, DOI: 10.1039/D0NR01602K.

Electrostatically modulated magnetophoretic transport of functionalised iron-oxide nanoparticles through hydrated networks.

Factors that determine magnetophoretic transport of magnetic nanoparticles (MNPs) through hydrated polymer networks under the influence of an external magnetic field gradient were studied. Functionalised iron oxide cores (8.9 nm core diameter) were tracked in real-time as they moved through agarose gels under the influence of an inhomogeneous magnetic field. Terminal magnetophoretic velocities were observed in all cases, these were quantified and found to be highly reproducible and sensitive to the conditions. Increasing agarose content reduced magnetophoretic velocity, we attribute this to increasingly tortuous paths through the porous hydrated polymer network and propose a new factor to quantify the tortuosity. The impact of MNP surface functionalisation, charge, network fixed charge content, and ionic strength of the aqueous phase on velocity were studied to separate these effects. For MNPs functionalised with polyethylene glycol (PEG) increasing chain length reduced velocity but the tortuosity extracted, which is a function of the network, was unchanged; validating the approach. For charged citrate- and arginine-functionalised MNPs, magnetophoretic velocities were found to increase for particles with positive and decrease for particles with negative zeta potential. In both cases these effects could be moderated by reducing the number of agarose anionic residues and/or increasing the ionic strength of the aqueous phase; conditions under which tortuosity again becomes the critical factor. A model for MNP transport identifying the contributions from the tortuous pore network and from electrostatic effects associated with the pore constrictions is proposed.

Luminescent lanthanide (Eu(iii)) cross-linked supramolecular metallo co-polymeric hydrogels: the effect of ligand symmetry.

Two lanthanide luminescent naphthyl-dipicolinic amide (dpa) methacrylate monomers for the synthesis of grafted supramolecular co-polymer gels (hydrogels), and their use as additional crosslinks in robust covalently cross-linked HEMA hydrogels is presented; the results demonstrate the importance of the ligand symmetry for the Eu(iii) emission from the hydrogels.