Core-shell Structure Research Articles

Dressing AgNWs with MXenes Nanosheets: Transparent Printed Electrodes Combining High-Conductivity and Tunable Work Function for High-Performance Opto-Electronics.

High-work function transparent electrodes (HWFTEs) are key for establishing Schottky and Ohmic contacts with n-type and p-type semiconductors, respectively. However, the development of printable materials that combine high transmittance, low sheet resistance, and tunable work function remains an outstanding challenge. This work reports a high-performance HWFTE composed of Ag nanowires enveloped conformally by Ti3C2Tx nanosheets (TA), forming a shell-core network structure. The printed TA HWFTEs display an ultrahigh transmittance (>94%) from the deep-ultraviolet (DUV) to the entire visible spectral region, a low sheet resistance (<15 Ωsq-1), and a tunable work function ranging from 4.7 to 6.0eV. The introduction of additional oxygen terminations on the Ti3C2Tx surface generates positive dipoles, which not only increases the work function of the TA HWFTEs but also elevates the TA/Ga2O3 Schottky barrier, resulting in a high self-powered responsivity of 18mAW-1 in Ga2O3 diode DUV photodetectors, as demonstrated via experimental characterizations and theoretical calculations. Furthermore, the TA HWFTEs-based organic light-emitting transistors exhibit exceptional emission brightness of 5020cd m-2, being four-fold greater than that in Au electrodes-based devices. The innovative nano-structure design, work function tuning, and the revealed mechanisms of electrode-semiconductor contact physics constitute a substantial advancement in high-performance optoelectronic technology.

Analysis of mechanical properties and stress distribution in self-healing microcapsules using micro-compressive test, nanoindentation test, and finite element analysis

Abstract This study analyzed self-healing microcapsules composed of melamine, urea, and formaldehyde (MUF). The thin shell’s mechanical properties were predicted using various techniques to gain a comprehensive understanding of their behavior. The compressive behavior of the microcapsules was assessed through micro-compression testing. The elastic modulus of the thin shell was precisely determined using nanoindentation, a method known for its accuracy in measuring material properties. Finite element analysis (FEA) was then applied, modeling the microcapsule between two plates and treating the core, which contains the healing agent, as an incompressible liquid. The mechanical properties of the thin shell, based on the elastic modulus derived from the nanoindentation test, were incorporated into the FEA, and the results were compared with those from the micro-compression test. Additionally, we analyzed the von Mises stress distribution to evaluate stress concentration within the spherical core–shell structure, ensuring the reliability of our conclusions. The test methods and analysis techniques presented in this study provide guidelines for improving the stiffness of MUF microcapsules. They can be further applied to predict the properties of materials with a spherical core–shell structure.

Formation of core–shell structures and viscous fingering in cellulose beads regenerated from [DBNH][OAc]/DMSO

AbstractSuperbase Ionic Liquids (SBILs) are efficient direct-dissolution solvents for cellulose and have found applications such as manufacturing of man-made textile fibers. In this study cellulose beads were prepared from microcrystalline cellulose dissolved in a mixture of SBIL 1,5-diazabicyclo[4.3.0]non-5-enium acetate with dimethyl sulfoxide, [DBNH][OAc]/DMSO, by drop-wise regeneration using water as an antisolvent. This resulted in cellulose regeneration by spinodal decomposition phase separation. The cross-sections of freeze-dried beads were thoroughly investigated using SEM, revealing a complex internal bead structure. Special attention was paid to structures resulting from the inwards moving regeneration front, where the solvent and antisolvent interdiffuse in opposite directions. The phase boundary at the regeneration front showed evidence of Saffman–Taylor instability, i.e., viscous fingering. Altering the diffusion environment surrounding the bead during regeneration resulted in nested layers of cores and shells. The number and placement of the core–shell separations was regulated by the number of transfers between two antisolvent baths and the duration of alternating periods of fast and slow interdiffusion of water and [DBNH][OAc]/DMSO through the bead perimeter. Graphical abstract

LnIII/CuI Bimetallic Nanoclusters with Enhanced NIR-II Luminescence.

Coinage-metal clusters with excellent luminescence properties have attracted considerable interest due to their intriguing structures and potential applications. However, achieving strong near-infrared (NIR) luminescence in these clusters is highly challenging. Here, we have successfully synthesized the first LnIII/CuI bimetallic clusters, formulated as [LnCu54O6Cl3(2-MeO-PhC≡C)36] (ClO4)6 (Ln = Yb for YbCu54, Er for ErCu54, and Gd for GdCu54). Single crystal X-ray diffraction showed that the LnCu54 clusters have a three-layered core-shell structure, consisting of (LnO6)@Cu18Cl3@Cu36 units protected by 36 2-MeO-PhC≡C- ligands. Notably, the YbCu54 cluster exhibits significant NIR-II luminescence at 986 nm with the solid quantum efficiency of 33.3%, the highest among Cu clusters with NIR-II emission. This work not only reports the first category of LnIII/CuI clusters but also presents a method to enhance NIR luminescence in coinage-metal clusters through the incorporation of LnIII ions.

High Coverage Sub-Nano Iridium Cluster on Core-Shell Cobalt-Cerium Bimetallic Oxide for Highly Efficient Full-pH Water Splitting.

The construction of sub-nanometer cluster catalysts (<1nm) with almost complete exposure of active atoms serves as a promising avenue for the simultaneous enhancement of atom utilization efficiency and specific activity. Herein, a core-shell cobalt-cerium bimetallic oxide protected by high coverage sub-nanometer Ir clusters (denoted as Ir cluster@CoO/CeO2) is constructed by a confined in situ exsolution strategy. The distinctive core-shell structure endows Ir cluster@CoO/CeO2 with enhanced intrinsic activity and high conductivity, facilitating efficient charge transfer and full-pH water splitting. The Ir cluster@CoO/CeO2 achieves low overpotentials of 49/215, 52/390, and 54/243mV at 10mAcm-2 for hydrogen evolution reaction/oxygen evolution reaction (HER/OER) in 0.5m H2SO4, 1.0m PBS, and 1.0m KOH, respectively. The small decline in performance after 300h of operation renders it one of the most effective catalysts for full-pH water splitting. DFT calculations indicate that oriented electron transfer (along the path from Ce to Co and then to Ir) creates an electron-rich environment for surface Ir clusters. The reconstructed interface electronic environment provides optimized intermediates adsorption/desorption energy at the Ir site (for HER) and at the Ir-Co site (for OER), thus simultaneously speeding up the HER/OER kinetics.

Sub-10 nm PdNi@PtNi Core–Shell Nanoalloys for Efficient Ethanol Electro-Oxidation

By controlling the structure and composition of Pt-based nanoalloys, the ethanol oxidation reaction (EOR) performances of Pt alloy catalysts can be effectively improved. Herein, we successfully synthesis sub-10 nm PdNi@PtNi nanoparticles (PdNi@PtNi NPs) with a core–shell structure by a one-pot method. The sub 10 nm core–shell nanoparticles possess more effective atoms and exhibit a synergistic effect which can lead to a shift in the d-band center and alter binding energies toward adsorbates. Due to the synergistic effect and unique core–shell structure, the PdNi@PtNi NP catalysts exhibit excellent electrocatalytic performance for ethanol oxidation reactions in alkaline, achieving 9.30 times more mass activity and 7.05 times more specific activity that of the state-of-the-art Pt/C catalysts. Moreover, the stability of PdNi@PtNi NPs was also greatly improved over PtNi nanoparticles, PtPd nanoparticles, and commercial Pt/C. This strategy provides a new idea for improving the electrocatalytic performance of Pt-based catalysts for EORs.

Fast and on-site detection of fenthion in rice using core-shell Au@Ag nanoparticles and a portable Raman spectrometer

The residue of pesticide fenthion is a common issue in food safety, and how to conveniently detect it is a challenge in the food industry. Therefore, combined with a portable Raman spectrometer, a surface enhanced Raman spectroscopy (SERS) method based on a high-performance substrate Au@AgNPs had been designed for the rapid and sensitive detection of fenthion. Au@AgNPs can be induced to generate more hot spots to improve SERS signals because of their core-shell structure. The quantitative detection of fenthion was achieved under the optimal conditions: pH 7.0, 10−3 M CaCl2, 70 % Au@AgNPs concentration, and 4 min of incubation time. The results showed that the method had a wider detection range of 0.1–100 mg/L, a low detection limit (LOD) of 0.036 mg/L, excellent anti-interference ability, and reproducibility. In addition, the method was successfully validated with the actual sample rice. Therefore, the method had the advantages of being fast, on-site, and easy to use, which is useful for promoting its application.

Cascade enzyme-mimicking with spatially separated gold-ceria for dual-mode detection of superoxide anions

Metal-semiconductor nanozyme of dumbbell Au-CeO2 with spatially separated heterostructure has cascade superoxide dismutase (SOD)-like and peroxidase (POD)-like activities for superoxide anions detection. It was synthesized by selective growth of CeO2 at the ends of Au nanorod (Au NR). Taking advantage of the excellent local surface plasmon resonance (LSPR) effect of Au NR, the spatially separated Au-CeO2 has a higher photothermal effect than the continuously growing core-shell structure of Au@CeO2. Meanwhile, the hot electrons of Au NR could transfer to CeO2 under 808 nm laser irradiation, changing the ratio of Ce3+/Ce4+ redox couples over CeO2 and facilitating H2O2 decomposition thus enhancing POD-like activity. Based on the SOD-like activity of Au-CeO2, superoxide anion (O2·−) can be transformed into hydrogen peroxide (H2O2). Dual-mode including absorbance and temperature sensing detection of O2·−, with the detection range from nM to μM i.e., 0.1–150 μM and LOD of 0.033 μM (S/N = 3) was achieved through the cascade catalysis and photothermal effect. The as-proposed method was applicable to both cancer and normal cell samples with satisfactory accuracy and recovery.

A multifunctional platform based on ZIF-67 templated NiCo-LDH and Fe3O4 hollow spheres for photocatalytic CO2 conversion and supercapacitors

This work presented a series of hybrid materials F@P-LDHs exhibiting the core-shell structure with PPy as the interface modifier, explored as dual-functional materials for studying photocatalytic reduction of CO2 and electrochemical behaviors. F@P-LDHs served as photocatalysts, effectively convert CO2 into CO without using any sacrificial agents and photosensitizers via the gas-solid mode under the visible light irradiation. The generation rate of CO was as high as 10.32 μmol g−1h−1, which was 5.4 and 6.4 times higher than the original Fe3O4@PPy and NiCo-LDH. The well performance might be ascribed to the generation of type Z heterojunction with the interface modifier PPy, jointly accelerating the separation and migration of photo-generated charge carriers between Fe3O4@PPy and NiCo-LDH. Besides, F@P-LDHs were also developed as supercapacitors, and their electrochemical behaviors were investigated. Their good electrochemical performances were attributed to the synergistic effect among hollow Fe3O4 microspheres, polypyrrole and NiCo-LDH. Therefore, as dual-functional materials, the hybrid materials have great potential in the field of CO2 conversion and supercapacitors.

Effect of T’-YSZ@Al2O3 core-shell structure on fracture toughness of YSH24 ceramics

To meet the demands of higher operating temperatures in aero-engines, yttrium oxide fully stabilized cubic (C) phase hafnium oxide (YFSH) has emerged as a promising candidate for thermal barrier coatings due to its ultra-high melting and phase transition temperatures. However, its application is constrained by its inherently low fracture toughness. To enhance the fracture toughness of C-HfO2 phase ceramic, the metastable non-equilibrium tetragonal (T’) phase of Y0.08Zr0.92O1.96 (YSZ8) was synthesized using the sol-gel method. An Al2O3 layer was then coated on YSZ, forming a T’-YSZ@Al2O3 core-shell structure (with Al2O3 comprising 20 % of the YSZ volume). The phase organization stability and diffusion resistance of this T’-YSZ@Al2O3 core-shell structure were investigated. Composite ceramic bulks, with compositions x T’-YSZ@Al2O3/(1-x) YSH24 (where x is the volume fraction, x = 0, 0.1, 0.2, 0.3, 0.4), were prepared using spark plasma sintering (SPS). The impact of the T’-YSZ@Al2O3 addition on the fracture toughness of the YSH24 matrix and the toughening mechanisms were analyzed. The results indicate that the introduction of the T’-YSZ@Al2O3 core-shell structure with good structural integrity into YSH24 ceramics prevents phase transitions. As the volume fraction of the core-shell structure increases from x = 0–0.4, the fracture toughness initially rises and then decreases, reaching a maximum of 2.36 MPa·m1/2 at x = 0.3. This value represents a 38.8 % improvement compared to that of the single C-HfO2 phase YSH24 bulks. The primary toughening mechanism is attributed to the ferroelastic domain switching of T’-YSZ within the T’-YSZ@Al2O3 core-shell structure.

Core-shell MIL-53(Al)–NH2@UiO-66 coated solid-phase microextraction Arrow for the selective enrichment of nine alkylphenols in milk

Metal-organic frameworks (MOFs) hold significant potential for sample preparation, but single-MOF materials often face limitations in selectivity and extraction efficiency. To overcome these, a mesoporous MIL-53(Al)–NH2@UiO-66 composites with a core–shell structure was synthesized using an epitaxial growth strategy. This composite leverages the complementary properties of both MOFs, offering enhanced active sites and interaction forces for analytes. The structure and integration of the composite were characterized using Fourier-transform infrared spectroscopy, scanning electron microscopy, and X-ray diffraction, confirming their successful integration. To address the challenge of detecting alkylphenols (APs) in food matrices, known for their endocrine-disrupting properties and low concentrations, a new solid-phase microextraction (SPME) Arrow was fabricated using the MIL-53(Al)–NH2@UiO-66 composite combined with polyacrylonitrile as a binder. APs were detected using ultra-performance liquid chromatography and quadrupole time-of-flight tandem mass spectrometry (UPLC-ESI-Q-ToF/MS). The developed SPME Arrow-UPLC-ESI-Q-ToF/MS method exhibits good linearity (R2 ≥ 0.9958), wide linear range (0.01–1000 μg L–1), and high sensitivity (limits of detection ranging from 0.005 to 0.01 μg L–1) for APs determination. This method was validated for determining nine APs in milk samples from various packing materials, with spiked recoveries ranging from 85.2 % to 115 % and relative standard deviations from 3.4 % to 13.6 %. This study demonstrates the potential of MOF-on-MOF composites in enhancing the performance of adsorbents for SPME pretreatment, offering a promising approach for improving analytical methodologies in food safety.

Preparation of core-shell Si/C/graphene composite for high-performance lithium-ion battery anodes

One of the important objectives for the development of enhanced lithium-ion batteries is developing high-performance silicon-based anodes with durable operational capability. Herein, a three-dimensional graphene-decorated core-shell Si/C composite is fabricated by the in-situ polymerization of organic pyrrole molecule and pyrolysis process, in which the melamine formaldehyde resin is subtly used as three-dimensional porous framework to offer abundant loading area for the uniform dispersion of active silicon nanoparticles. Meanwhile, the core-shell structure deriving from polypyrrole in the composite can effectively buffer the volume change of silicon ingredient and avoid the direct contact with the electrolyte during the cycling process, leading to the improved structural stability and electrochemical performance. The outermost layer of graphene nanosheets is designed to enhance the electrical conductivity of the electrode. As a result, the synthesized Si/C/graphene composite exhibits a high capacity and excellent cycling performance. This work reveals that combining a three-dimensional carbon substrate with a core-shell structure might be a promising solution for anode materials with obvious volume transformation.

Improved Interfacial Interactions by Core-Shell CoFe2O4@SiO2 Composites to Enhance the Ability of Corrosion Resistance and Electromagnetic Wave Absorption.

With the rapid development of science and technology, stealth and anti-corrosion activities in oceans have attracted widespread attention. This study successfully prepares CoFe2O4@SiO2 with a core-shell structure. This core-shell structure endows the CoFe2O4@SiO2 with good impedance matching and interfacial polarization. Thus, the CoFe2O4@SiO2 exhibits an excellent electromagnetic wave absorption performance with a minimum reflection loss of -45.16dB. Moreover, the CoFe2O4@SiO2 exhibits an excellent dispersion ability in epoxy. The corrosion resistance of the CoFe2O4@SiO2/epoxy is enhanced. After 60 days of immersion, the low-frequency impedance modulus of the CoFe2O4@SiO2/epoxy is still >109Ωcm2. The CoFe2O4@SiO2 realize the dual functions of stealth and anti-corrosion, which provide ideas for developing marine stealth applications.

Dramatic droplet deformation through interfacial particles jamming

Droplets of one fluid in a second, immiscible fluid are typically spherical in shape due to the interfacial tension between the two fluids. Shear forces can lead to droplet deformation when they are subjected to flow, and these effects can be further modified when the droplet is stabilized by a surfactant due to a flow-induced gradients in the surfactant concentration. An alternative method of stabilizing droplets is through the use of colloidal particles, whose stabilization behavior is intrinsically different from molecular surfactants. Under the same flow condition, a gradient of particle concentration can result in the jamming of particles in regions with a high packing density, making the interface solid-like, albeit only under compression and not tension. However, how this asymmetry in the surfactant properties alters the droplet shape under shear is unknown. Here, we show that shear of particle-stabilized droplets can lead to a remarkable array of shape deformations as the droplets flow through a constrained microchannel. The shear-induced migration of particles on the surface results in the formation of an elastic shell at the back of the droplet, which can wrinkle and invaginate, ultimately leading to a unique core-shell structure. The shapes depend on the Peclet number of the flow, reflecting the balance of shear forces that drive the particles and diffusion that randomizes them. These findings highlight the consequences of the asymmetry in the forces between the particles and provide a unique method to controllably create droplets with a vast array of different shapes.

Preparation of a branched hierarchical Co3O4@Fe2O3 core–shell structure with high-density catalytic sites for efficient catalytic conversion of nitrate in wastewater to ammonia

This work employs a high-efficiency, low cost and environmentally friendly electrochemical nitrate reduction (NO3RR) strategy to realize the highly selective conversion of a typical environmental pollutant-nitrate to an extremely important chemical product-ammonia. To ensure high ammonia selectivity and Faradaic efficiency, a branched hierarchical Co3O4@Fe2O3 core–shell structure was synthesized on carbon cloth (CC) using a simple two-step hydrothermal method. After material characterization and parameter optimization, a nitrate conversion rate of 88.4 %, ammonia selectivity of 89.4 %, Faradaic efficiency of 87.2 % and NH3-N yield rate of 3810 μg h−1 cm−2 were obtained at Co3O4@Fe2O3|CC, which also displayed durability by retaining a high Faradaic efficiency of 79.3 % after six consecutive NO3RR cycles. Investigation of the mechanism reveals that active atomic *H plays a key role in the NO3RR. The excellent NO3RR performance of Co3O4@Fe2O3|CC is attributed to its branched hierarchical core–shell structure with large electrochemical surface area and fully exposed catalytic sites. In addition, both experimental and density functional theory (DFT) calculations indicate that the Co3O4@Fe2O3 core–shell structure is superior to Co3O4|CC and Fe2O3|CC in catalyzing NO3RR due to the synergistic effect between Co3O4 and Fe2O3. This synergistic effect can promote the adsorption of NO3–, release of NH3 and inhibition of hydrogen evolution, ensuring the highly selective and efficient conversion of NO3– to NH3. This work demonstrates that the morphology of an electrocatalyst can significantly affect its performance for the NO3RR, and has potential for practical application purposes.

Exploiting inhalable microparticles incorporating hybrid polymer-lipid nanoparticles loaded with Iloprost manages lung hyper-inflammation

This study focuses on developing of a novel inhalation therapy for managing lung hyper-inflammation, producing hybrid polymer-lipid nanoparticles loaded with Iloprost (Ilo). These nanoparticles showed a size of approximately 100 nm with a core–shell structure and provided prolonged drug release, reaching 28 wt% after 6 h of incubation. The phospholipid composition and quantity (64 wt% on the total sample weight) result in minimal interaction with mucin and a significant effect on the rheology of a cystic fibrosis mucus model, in terms of reducing complex viscosity.To obtain an inhalable microparticulate matrix suitable for incorporating Ilo@PEG-LPHNPs, the qualitative and quantitative composition of the feed fluid for the spray drying (SD) process was optimized. The selected composition (10 % wt/vol of mannitol and 10 % wt of ammonium bicarbonate relative to the weight of mannitol) was used to produce Nano-into Microparticles (NiM). The characterization of NiM revealed excellent aerodynamic properties, with a Mass Median Aerodynamic Diameter (MMAD) of 4.34 μm and a Fine Particle Fraction (FPF) of approximately 57 %. Biological characterization revealed that the particles are non-toxic to 16-HBE cells and can effectively evade macrophage uptake, likely due to the presence of PEG in their composition. Moreover, the delivered Iloprost significantly downregulates the production of the pro-inflammatory cytokine IL-6, showing the therapeutic potential of this drug delivery system.

Light-Responsive Smart Nanoliposomes: Harnessing the Azobenzene Moiety for Controlled Drug Release under Near-Infrared Irradiation.

The azobenzene moiety is an intriguing structure that deforms under UV and visible light, indicating a high potential for biomedical applications. However, its reaction to UV radiation is problematic because of its high energy and low tissue penetration. Unlike previous research on azobenzene structures in photoresponsive materials, this study presents a novel method for imparting photostimulation-responsive properties to liposomes by incorporating the azobenzene moiety and extending the light wavelength with up-conversion nanoparticles. First, the azobenzene structure was incorporated into a phospholipid molecule to create Azo-PSG, which could spontaneously form vesicle assemblies in aqueous solutions and isomerizes within 1 h of light exposure. Furthermore, orthogonal up-conversion nanoparticles with a core-shell structure were created by sequentially growing lanthanide rare earths in the shell layer, which efficiently converts near-infrared light into ultraviolet (400 nm) and blue-green (540 nm) light. Combining these core-shell structured up-conversion nanomaterials with Azo-PSG molecules resulted in the creation of a near-infrared light-responsive smart nanoliposome system. Under near-infrared light irradiation, UCNPs emit UV and blue-green light, causing conformational changes in Azo-PSG molecules that allow drug release within 6 h. The reversible structural shift of Azo-PSG in response to light stimulation holds enormous promise for improving drug release techniques. This novel technique also expands the usage of UV-responsive compounds beyond their constraints of low penetration and high biotoxicity, allowing for rapid medication release under NIR light.

A novel core–shell structure composed of polypyrrole shell and high-entropy oxide/carbon cloth core for high-performance supercapatteries

High-entropy oxides (HEOs) are promising candidates for supercapattery applications owing to their unique high entropy effect and abundant metal elements to provide high capacitance. However, their poor electrical conductivity, low specific capacitance, and limited stability still need to be addressed. Herein, coaxial core–shell structured electrodes (CoCrFeMnNi)3O4@CC-PPy are prepared by a two-step electrodeposition method. The core–shell electrode structure is formed by depositing (CoCrFeMnNi)3O4 (HEO) nanoparticles on a conductive carbon (CC) cloth followed by electrodeposition of a shell layer composed of highly conductive polypyrrole (PPy) nanospheres. The optimized HEO@CC-PPy-140s electrode prepared by electrodeposition for 140 s exhibits excellent specific capacitance reaching 791 F·g−1 at a current density of 0.5 A·g−1, and a specific capacitance retention of 63 % at a high current density of 10 A·g−1. Importantly, the use of HEO@CC-PPy as a negative electrode in a supercapattery device assembled with an electrodeposited NiCo2O4@CC positive electrode displays a high energy density of 49.2 Wh·kg−1 and good cycling stability, with a capacitance retention rate of 88.2 % after 3000 charge/discharge cycles. Overall, the proposed coaxial core–shell structure electrode design offers promising potential for the fabrication of supercapatteries with advanced characteristics.

Multispectral compatible anti-reconnaissance strategy: Implementing a modulation system integrating visible light-hyperspectral-radar wave

To tackle the challenges of multi-spectral reconnaissance technology, a pioneering anti-reconnaissance device that integrates visible-light, hyperspectral, and microwave radar functionalities has been developed for the first time. By oxidative polymerization method to create a core–shell Fe3O4@polyaniline composite material for the counter electrode. This design optimized impedance matching, achieving wideband radar wave absorption up to 10.5 GHz (reflection loss < -10 dB). The core–shell structure enhanced specific surface area, improving charge exchange and electrochemical performance to meet stringent counter electrode requirements. And, constructed a frequency-selective metal electrode based on metamaterial principles, complementing the radar wave absorption capabilities of the counter electrode material. Additionally, synthesized an asymmetric viologen molecule as the working electrode, mimicking vegetation color transitions from green to yellow while preserving hyperspectral characteristics and radar wave absorption properties. To enhance hyperspectral compatibility without compromising radar wave absorption or color dynamics, we developed a cross-linked polyvinyl alcohol/hydroxyethyl cellulose film based on biomimetic principles. The device can switch between yellow and green under voltages of 0 or −1.2 V, with both states exhibiting a spectral similarity to foliage exceeding 0.95 and an effective bandwidth reaching 13.44 GHz. The integration of these three functionalities allows the device to operate independently without interference.

Facile Preparation of Raspberry-Like SiO2@Polyurea Microspheres with Tunable Wettability and Their Application for Oil-Water Separation.

Raspberry-like microspheres have been widely used as superhydrophobic materials, photonic crystals, drug carriers, etc. Nevertheless, their preparation methods, usually consisting of multiple steps, are generally time- and energy-consuming. Herein raspberry-like SiO2@polyurea microspheres (SiO2@PUM) are readily prepared via a one-step precipitation polymerization of isophorone diisocyanate in a H2O/acetone mixture with the presence of SiO2 particles. The sphere size, surface roughness, and SiO2 content of SiO2@PUM are easily adjustable by varying the experimental conditions. TEM and SEM observations reveal that the final SiO2@PUM exhibits a core-shell structure, with polyurea (PU) in the core and SiO2 particles as the shell. In the process, the SiO2 particles were initially located on the PUM surface as a monolayer. With the reaction proceeding, the monolayer of SiO2 particles became thicker, forming a thicker layer of SiO2 particles on PUM due to the accumulation of SiO2 particles, leading to a multilayer structure of SiO2 particles on the shell of SiO2@PUM. The formation mechanism of the raspberry-like SiO2@PUM was thoroughly discussed and ascribed to electrostatic attraction between the positively charged PU and negatively charged SiO2 particles. Once dried, SiO2@PUM was superhydrophobic and turned hydrophilic if water-wetted. Using a layer of SiO2@PUM, effective separation with good reusability for a variety of oil-water mixtures was achieved regardless of the oil density and types of oil-water emulsions. This work presents a novel protocol for the preparation of raspberry-like microspheres with tunable wettability via a rapid and green process, and the resulting microspheres are highly effective for the separation of diverse types of oil-water mixtures.