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Water pollution is a global issue as a consequence of rapid industrialization and urbanization. Organic compounds which are generated from various industries produce problematic pollutants in water. Recently, metal oxide (TiO2, SnO2, CeO2, ZrO2, WO3, and ZnO)-based semiconductors have been explored as excellent photocatalysts in order to degrade organic pollutants in wastewater. However, their photocatalytic performance is limited due to their high band gap (UV range) and recombination time of photogenerated electron–hole pairs. Strategies for improving the performance of these metal oxides in the fields of photocatalysis are discussed. To improve their photocatalytic activity, researchers have investigated the concept of doping, formation of nanocomposites and core–shell nanostructures of metal oxides. Rare-earth doped metal oxides have the advantage of interacting with functional groups quickly because of the 4f empty orbitals. More precisely, in this review, in-depth procedures for synthesizing rare earth doped metal oxides and nonocomposites, their efficiency towards organic pollutants degradation and sources have been discussed. The major goal of this review article is to propose high-performing, cost-effective combined tactics with prospective benefits for future industrial applications solutions.

External manipulation of emission colour is of significance for scientific research and applications, however, the general stimulus-responsive colour modulation method requires both stringent control of microstructures and continously adjustment of particular stimuli conditions. Here, we introduce pathways to manipulate the kinetics of time evolution of both intensity and spectral characteristics of X-ray excited afterglow (XEA) by regioselective doping of lanthanide activators in core-shell nanostructures. Our work reported here reveals the following phenomena: 1. The XEA intensities of multiple lanthanide activators are significantly enhanced via incorporating interstitial Na + ions inside the nanocrystal structure. 2. The XEA intensities of activators exhibit diverse decay rates in the core and the shell and can largely be tuned separately, which enables us to realize a series of core@shell NPs featuring distinct time-dependent afterglow colour evolution. 3. A core/multi-shell NP structure can be designed to simultaneously generate afterglow, upconversion and downshifting to realize multimode time-dependent multicolour evolutions. These findings can promote the development of superior XEA and plentiful spectral manipulation, opening up a broad range of applications ranging from multiplexed biosensing, to high-capacity information encryption, to multidimensional displays and to multifunctional optoelectronic devices. X-ray activated afterglow nanomaterials are desirable components for advanced optoelectronic applications. Here, the authors present pathways to modulate the stimulus-responsive color emissions in lanthanide-doped fluoride core-shell nanoparticles.

The development of Pt-based core/shell nanoparticles represents an emerging class of electrocatalysts for fuel cells, such as methanol oxidation reaction (MOR) and ethanol oxidation reaction (EOR). Here, we present a one-pot synthesis approach to prepare hexagonal PtBi/Pt core/shell nanostructure composed of an intermetallic Pt 1 Bi 1 core and an ultrathin Pt shell with well-defined shape, size, and composition. The structure and the synergistic effect among different components enhanced their MOR and EOR performance. The optimized Pt 2 Bi nanoplates exhibit excellent mass activities in both MOR (4,820 mA·mgPt –1 ) and EOR (5,950 mA·mgPt –1 ) conducted in alkaline media, which are 6.15 times and 8.63 times higher than those of commercial Pt/C, respectively. Pt 2 Bi nanoplates also show superior operation durability to commercial Pt/C. This work may inspire the rational design and synthesis of Pt-based nanoparticles with improved performance for fuel cells and other applications.

With the pace of time, synthesis of nanomaterials has paved paths to blend two or more materials having different properties into hybrid nanoparticles. Therefore, it has become possible to combine two different functionalities in a single nanoparticle and their properties can be enhanced or modified by coupling of two different components. Core–shell technology has now represented a new trend in analytical sciences. Core–shell nanostructures are in demand due to their specific design and geometry. They have internal core of one component (metal or biomolecules) surrounded by a shell of another component. Core–shell nanoparticles have great importance due to their high thermal stability, high solubility and lower toxicity. In this review, recent progress in development of new and sophisticated core–shell nanostructures has been explored. The first section covers introduction throwing light on basics of core–shell nanoparticles. Following section classifies core–shell nanostructures into single core/shell, multicore/single shell, single core/multishell and multicore/multishell nanostructures. Next main section gives a brief description on types of core–shell nanomaterials followed by processes for the synthesis of core–shell nanostructures. Ultimately, the final section focuses on the application areas such as drug delivery, bioimaging, solar cell applications etc.Graphic abstract

In this study, three kinds of electrohydrodynamic atomization (EHDA) processes (electrospraying, electrospinning, and coaxial electrospinning) are implemented to create hydroxypropyl methylcellulose (HPMC) based ultra‐thin products for providing the fast dissolution of a poorly water‐soluble drug ketoprofen (KET). An EHDA apparatus, characterized by a novel spinneret, is homemade for conducting the three processes. The three types of products are electrospun nanofibers E1, electrosprayed microparticles E2, and core‐shell nanofibers E3. SEM and TEM results indicate that they have the anticipated morphologies and inner structures. X‐ray diffraction and Fourier Transform Infrared results verify that KET is mainly amorphous in all the composites due to its fine compatibility with HPMC. In vitro dissolution tests demonstrate that the drug rapid release performances has an order of E3>E1>E2≫KET powders. The fast dissolution mechanisms are suggested and the advantages of the three products are compared. The super performance of E3 in furnishing the rapid release is attributed to a synergistic action of small size (of the shell thickness), high porosity, amorphous state of drug, and the solubility of HPMC. EHDA nanostructures can support the development of nano drug delivery systems (DDSs) through tailoring the spatial distribution of drug molecules within the nano products.

Defect and interface engineering are efficient approaches to adjust the physical and chemical properties of nanomaterials. In order to effectively utilize these strategies for the improvement of microwave absorption properties (MAPs), in this study, we reported the synthesis of hollow carbon shells and hollow carbon@MoS 2 nanocomposites by the template-etching and template-etching-hydrothermal methods, respectively. The obtained results indicated that the degree of defect for hollow carbon shells and hollow carbon@MoS 2 could be modulated by the thickness of hollow carbon shell, which effectively fulfilled the optimization of electromagnetic parameters and improvement of MAPs. Furthermore, the microstructure investigations revealed that the precursor of hollow carbon shells was encapsulated by the sheet-like MoS 2 in high efficiency. And the introduction of MoS 2 nanosheets acting as the shell effectively improved the interfacial effects and boosted the polarization loss capabilities, which resulted in the improvement of comprehensive MAPs. The elaborately designed hollow carbon@MoS 2 samples displayed very outstanding MAPs including strong absorption capabilities, broad absorption bandwidth, and thin matching thicknesses. Therefore, this work provided a viable strategy to improve the MAPs of microwave absorbers by taking full advantage of their defect and interface engineering.

HighlightsThree-dimension hierarchical core–shell Mo2N@CoFe@C/CNT composites were successfully constructed via a fast MOF-based ligand exchange strategy.Abundant magnetic CoFe nanoparticles suspended within “nanotubes on microrods” matrix exhibited strong magnetic loss capability, confirmed by off-axis electron holography.Hierarchical Mo2N@CoFe@C/CNT composites displayed remarkable microwave absorption value of − 53.5 dB.Hierarchical magnetic-dielectric composites are promising functional materials with prospective applications in microwave absorption (MA) field. Herein, a three-dimension hierarchical “nanotubes on microrods,” core–shell magnetic metal–carbon composite is rationally constructed for the first time via a fast metal–organic frameworks-based ligand exchange strategy followed by a carbonization treatment with melamine. Abundant magnetic CoFe nanoparticles are embedded within one-dimensional graphitized carbon/carbon nanotubes supported on micro-scale Mo2N rod (Mo2N@CoFe@C/CNT), constructing a special multi-dimension hierarchical MA material. Ligand exchange reaction is found to determine the formation of hierarchical magnetic-dielectric composite, which is assembled by dielectric Mo2N as core and spatially dispersed CoFe nanoparticles within C/CNTs as shell. Mo2N@CoFe@C/CNT composites exhibit superior MA performance with maximum reflection loss of − 53.5 dB at 2 mm thickness and show a broad effective absorption bandwidth of 5.0 GHz. The Mo2N@CoFe@C/CNT composites hold the following advantages: (1) hierarchical core–shell structure offers plentiful of heterojunction interfaces and triggers interfacial polarization, (2) unique electronic migration/hop paths in the graphitized C/CNTs and Mo2N rod facilitate conductive loss, (3) highly dispersed magnetic CoFe nanoparticles within “tubes on rods” matrix build multi-scale magnetic coupling network and reinforce magnetic response capability, confirmed by the off-axis electron holography.

Core–shell particles with earth-abundant cores represent an effective design strategy for improving the performance of noble metal catalysts, while simultaneously reducing the content of expensive noble metals 1 – 4 . However, the structural and catalytic stabilities of these materials often suffer during the harsh conditions encountered in important reactions, such as the oxygen reduction reaction (ORR) 3 – 5 . Here, we demonstrate that atomically thin Pt shells stabilize titanium tungsten carbide cores, even at highly oxidizing potentials. In situ, time-resolved experiments showed how the Pt coating protects the normally labile core against oxidation and dissolution, and detailed microscopy studies revealed the dynamics of partially and fully coated core–shell nanoparticles during potential cycling. Particles with complete Pt coverage precisely maintained their core–shell structure and atomic composition during accelerated electrochemical ageing studies consisting of over 10,000 potential cycles. The exceptional durability of fully coated materials highlights the potential of core–shell architectures using earth-abundant transition metal carbide (TMC) and nitride (TMN) cores for future catalytic applications. Using core–shell particles represents an effective design strategy for improving the performance of noble metal catalysts, but their stabilities can suffer during reactions. Atomically thin Pt shells are shown to stabilize titanium tungsten carbide cores, even at highly oxidizing potentials.

CoS 2 is considered to be a promising electrocatalyst for hydrogen evolution reaction (HER). However, its further widespread applications are hampered by the unsatisfactory activity due to relatively high chemisorption energy for hydrogen atom. Herein, theoretical predictions of first-principles calculations reveal that the introduction of a Cl-terminated MXenes-Ti 3 CNCl 2 can significantly reduce the HER potential of CoS 2 -based materials and the Ti 3 CNCl 2 @CoS 2 core-shell nanostructure has Gibbs free energy of hydrogen adsorption (∣ΔG H ∣) close to zero, much lower than that of the pristine CoS 2 and Ti 3 CNCl 2 . Inspired by the theoretical predictions, we have successfully fabricated a unique Ti 3 CNCl 2 @CoS 2 core-shell nanostructure by ingeniously coupling CoS 2 with a Cl-terminated MXenes-Ti 3 CNCl 2 . Interface-charge transfer between CoS 2 and Ti 3 CNCl 2 results in a higher degree of electronic localization and a formation of chemical bonding. Thus, the Ti 3 CNCl 2 @CoS 2 core-shell nanostructure achieves a significant enhancement in HER activity compared to pristine CoS 2 and Ti 3 CNCl 2 . Theoretical calculations further confirm that the partial density of states of CoS 2 after hybridization becomes more non-localized, and easier to interact with hydrogen ions, thus boosting HER performance. In this work, the success of oriented experimental fabrication of high-efficiency Ti 3 CNCl 2 @CoS 2 electrocatalysts guided by theoretical predictions provides a powerful lead for the further strategic design and fabrication of efficient HER electrocatalysts.

The high catalytic performance of core–shell nanoparticles is usually attributed to their distinct geometric and electronic structures. Here we reveal a dynamic mechanism that overturns this conventional understanding by a direct environmental transmission electron microscopy visualization coupled with multiple state-of-the-art in situ techniques, which include synchrotron X-ray absorption spectroscopy, infrared spectroscopy and theoretical simulations. A Ni–Au catalytic system, which exhibits a highly selective CO production in CO 2 hydrogenation, features an intact ultrathin Au shell over the Ni core before and after the reaction. However, the catalytic performance could not be attributed to the Au shell surface, but rather to the formation of a transient reconstructed alloy surface, promoted by CO adsorption during the reaction. The discovery of such a reversible transformation urges us to reconsider the reaction mechanism beyond the stationary model, and may have important implications not only for core–shell nanoparticles, but also for other well-defined nanocatalysts. The structure of core–shell catalysts is often assumed to be conserved over a reaction. Now, an in situ study reveals that the shell of Ni@Au nanoparticles is reversibly converted into a Ni–Au alloy during CO 2 hydrogenation, with important mechanistic implications.