Multilayered Core Shell Structure Research Articles

Potentiometric enzymatic aptasensing of paralytic shellfish toxins using graphene-wrapped magnetic nanospheres and an all-solid-state cadmium-selective microelectrode

A highly sensitive potentiometric enzymatic aptasensing system for the detection of paralytic shellfish toxins (PSTs) is developed by integrating graphene-wrapped magnetic nanospheres (Fe3O4@SiO2@rGO) with an all-solid-state ion-selective microelectrode. The multilayered core-shell structure of Fe3O4@SiO2@rGO enhances the efficient adsorption of aptamer molecules tagged with cadmium sulfide (CdS) nanoparticles. These CdS-aptamer conjugates, when bound with PST molecules, can be desorbed from the Fe3O4@SiO2@rGO surface into the sample solution and subsequently digested by deoxyribonuclease I (DNase I). This digestion process releases the PST molecules for recirculation, significantly reducing the retention of CdS on the surface of Fe3O4@SiO2@rGO. After magnetic separation and acid dissolution, the released Cd2+ from the magnetic nanospheres are measured using an all-solid-state Cd2+-selective microelectrode, enabling sensitive potentiometric detection of PSTs. Using gonyautoxin 1/4 (GTX 1/4) as a model, the sensing system exhibits a linear concentration range from 5 to 150 pM and a low detection limit of 1.7 pM for GTX 1/4, and has been successfully applied in the analysis of seawater samples.

Enhanced red UC emission of Er3+ ions by constructing multi-heterojunction core-shell nanoparticles

The construction of core-shell structures with multiple heterojunctions facilitates ion energy transfer and minimizes surface quenching effects, which are essential for enhancing and regulating the upconversion emission of materials. In this study, we effectively regulated the spatial distribution of Yb3+ and Er3+ ions in multilayered heterogeneous core-shell structures to significantly enhance the red upconversion emission of Er3+ ions. Specifically, the red emission intensity of the NaErF4@NaYbF4: 2 %Er3+@NaYF4 core-shell nanoparticles was enhanced nearly 24.4-fold compared to that of NaErF4 nanoparticles. This enhancement results from a bidirectional energy transfer process. Moreover, when we swapped the positions of the NaErF4 core and the NaYbF4: 2 %Er3+ shell and introduced NaYF4 inert isolation layer and Yb3+ ions, the red emission intensity of the NaYbF4:2 %Er3+@NaYF4:20 %Yb3+@NaErF4@ NaYF4 multilayer core-shell structure increased significantly by nearly 254.3-fold compared to NaErF4 nanoparticles. The remarkable enhancement of the red emission of Er3+ ions is primarily attributed to a well-organized bidirectional energy transfer process between the heavily doped core and shell Er3+-Yb3+ ion pairs. The energy transfer behavior of these multi-heterojunction core-shell nanoparticles was studied based on their spectral characteristics. The multilayer heterogeneous core-shell nanoparticles exhibited colorful emissions under different excitation conditions, highlighting their potential for biomedical applications and colorful anti-counterfeiting.

Exploration of Unconventional excitation wavelength and dynamic emission in rare-earth doped multilayer core-shell Structures: Application for optical “Hard” and “Soft” switching

Optical switches are increasingly acknowledged for their potential advantages over mechanical counterparts in various domains. However, research on optical switches remains relatively nascent, primarily focusing on applications like anti-counterfeiting, switching chemical reactions, etc., while neglecting the control of photocurrent switching. Here, we have developed NaYF4:30 %Er-NaYF4-NaYF4:20 %Ho-NaYF4 core–shell nanocrystals with unique upconversion (UC) multi-color emission properties under 1530 nm, 980 nm and 1150 nm laser excitations. These nanocrystals allow for optical control of circuit switching by modulating photocurrent signals in photosensitive circuits. The UC emission is due to the self-sensitization of rare earth ions in the core and shell. By adjusting the intermediate shell thickness, we have optimized the luminescence and investigated the mechanism. Combining these nanocrystals with a WO3 quantum dots (QDs) photochromic hydrogel, dynamic variation of UC emissions could be realized. Moreover, by combining with a commercial silicon photodetector, we constructed a photosensitive circuit demonstrating the modulation of photocurrent signal output and realized the “hard switching” of rapid circuit cutoff. Furthermore, by using the photochromic effect of WO3 QDs, the “soft switching” of slow circuit cutoff and recovery were also achieved. This work has significant implications for the development and application such as energy management system and smart home of optical switches in various fields.

Core-Shell Interface Engineering Strategies for Modulating Energy Transfer in Rare Earth-Doped Nanoparticles.

Rare earth-doped nanoparticles (RENPs) are promising biomaterials with substantial potential in biomedical applications. Their multilayered core-shell structure design allows for more diverse uses, such as orthogonal excitation. However, the typical synthesis strategies-one-pot successive layer-by-layer (LBL) method and seed-assisted (SA) method-for creating multilayered RENPs show notable differences in spectral performance. To clarify this issue, a thorough comparative analysis of the elemental distribution and spectral characteristics of RENPs synthesized by these two strategies was conducted. The SA strategy, which avoids the partial mixing stage of shell and core precursors inherent in the LBL strategy, produces RENPs with a distinct interface in elemental distribution. This unique elemental distribution reduces unnecessary energy loss via energy transfer between heterogeneous elements in different shell layers. Consequently, the synthesis method choice can effectively modulate the spectral properties of RENPs. This discovery has been applied to the design of orthogonal RENP biomedical probes with appropriate dimensions, where the SA strategy introduces a refined inert interface to prevent unnecessary energy loss. Notably, this strategy has exhibited a 4.3-fold enhancement in NIR-II in vivo imaging and a 2.1-fold increase in reactive oxygen species (ROS)-related photodynamic therapy (PDT) orthogonal applications.

Low-cycle fatigue behavior and microstructure evolution of ODS steel pipes at high temperatures

Oxide-dispersion-strengthened (ODS) steels are candidate materials for application in advanced nuclear reactors. In this study, the low-cycle fatigue performances of 13Cr-ODS ferritic steel pipes were investigated at 600, 700, and 800 °C. Cyclic softening was observed at high strain amplitudes with an increase in the number of fatigue cycles. However, cyclic hardening appeared first, and then cyclic softening occurred at a low strain amplitude with the increase in the number of fatigue cycles. By comparing the cyclic stress–strain curves and the monotonic stress–strain curves, it was found that cyclic softening occurred regardless of the strain amplitude. The Coffin–Manson and Basquin equations were used to predict the fatigue of the pipes. Microstructure analysis indicated that cyclic softening was induced by the dynamic recovery and recrystallization, which reduced the number of low-angle grain boundaries in the deformed grains by promoting dislocation annihilation and reorganization. A complex multi-layer core–shell structure with a large size (∼500 nm) was observed.

In-situ Ag SPR assisted S-scheme ZnO-CdS multi-layer core-shell heterojunction for enhanced photocatalytic degradation: Energy band engineering and reactive dynamics

Constructing an efficient photocatalyst to accelerate charge separation with strong redox capacity is in pursuit all the way. Herein, a novel heterojunction was achieved for efficient organic degradation, which took advantages of S-scheme mechanism, metal surface plasma resonance (SPR) and unique morphology. The multi-layer core-shell structure can be regulated by aging time with template-free, and Ag nanoparticles were modified on the heterojunction by photochemical deposition in situ to facilitate electron transport and improve stability. S-scheme and SPR endues the heterojunction with broad light absorption, increased light utilization, efficient carrier separation, and strong redox capacity. An examination of reactive dynamics revealed that superoxide radicals and hydroxyl radicals are crucial for oxidative degradation. Introducing oxygen during the reaction process has been found to enhance the efficiency by 7 %. This article furnishes novel insights into a coordination of energy band engineering, structure regulation, as well as reaction process adjustment for facilitating photo-degradation reactions.

Preparation and properties of multilayer core-shell structure ammonium polyphosphate synergistic with THEIC for flame retardant LDPE

In this paper, a new type of highly efficient intumescent flame-retardant low-density polyethylene composite was prepared using two key technologies, namely, microencapsulation encapsulation technology and novel carbon formation technology. Precisely, β-cyclodextrin encapsulated modified ammonium polyphosphate@melamine formaldehyde resin (β-CDMCAPP@MF) was prepared by using Si-IFR synergistic flame retardant effect combined with the gel-solution method, and then flame retardant low-density polyethylene (LDPE) was prepared by compounding with tris-(2-hydroxyethyl) isocyanate (THEIC). The results showed that β-CDMCAPP@MF was modified with MF, β-CD, and silica coating. This modification resulted in excellent hydrophobicity and good compatibility with LDPE. The addition of IFR containing β-CDMCAPP@MF significantly improved the flame retardancy of the LDPE composites. Specifically, when 30 wt% of β-CDMCAPP@MF was added, the ultimate oxygen index of the composites reached 24.7 %, and V-0 grade and the tensile strength went 11.41 MPa. Compared with IFR/LDPE with the same proportion of MF@MCAPP and β-CD@MCAPP, the ultimate oxygen indices were increased by 9.72 % and 12.15 %, respectively. The introduction of THEIC into the flame retardant system resulted in a LOI value of 36.5 % and an FRI value of 2.523, which is 32.33 % higher than that of the composites containing 30 wt% of the flame retardant system (without THEIC). Cone calorimetry test results showed that introducing β-CDMCAPP@MF and THEIC significantly improved the smoke emission.

Multilayered Core–Shell Structure in an Impact Polypropylene Copolymer Investigated by Atomic Force Microscopy–Infrared

Multilayered Core–Shell Structure in an Impact Polypropylene Copolymer Investigated by Atomic Force Microscopy–Infrared

Heterostructure CoFe@(Co0.5Fe0.5)S@NCNT anchored on rice husk-based hierarchical porous carbon as a bifunctional cathode catalyst for Zn–air batteries

A bifunctional catalyst, characterized by its sea urchin-like morphology and multi-layer core–shell structure (CoFe@(Co0.5Fe0.5)S@NCNT), was synthesized within the restriction of RHPC' hierarchical pore structure.

Robust vibrational coherence protected by a core-shell structure in silver nanoclusters.

Vibrational coherence has attracted considerable research interests because of its potential functions in light harvesting systems. Although positive signs of vibrational coherence in metal nanoclusters have been observed, the underlying mechanism remains to be verified. Here, we demonstrate that robust vibrational coherence with a lifetime of 1 ps can be clearly identified in Ag44(SR)30 core-shell nanoclusters, in which an icosahedral Ag12 core is well protected by a dodecahedral Ag20 cage. Ultrafast spectroscopy reveals that two vibrational modes at around 2.4 THz and 1.6 THz, corresponding to the breathing mode and quadrupolar-like mode of the icosahedral Ag12 core, respectively, are responsible for the generation of vibrational coherence. In addition, the vibrational coherence of Ag44 has an additional high frequency mode (2.4 THz) when compared with that of Ag29, in which there is only one low frequency vibration mode (1.6 THz), and the relatively faster dephasing in two-layer Ag29 relative to that in Ag44 further supports the fact that the robust vibrational coherence in Ag44 is ascribed to its unique matryoshka-like core-shell structure. Our findings not only present unambiguous experimental evidence for a multi-layer core-shell structure protected vibrational coherence under ambient conditions but also offers a practical strategy for the design of highly efficient quantum optoelectronic devices.

Enhancement in ignition and combustion of solid propellants by interfacial modification of Al/AP composites with transition metals

To improve the ignition and combustion behaviors of Al, the strategy of interfacial modification using transition metals (TMs) for the Al/AP composites to produce the multi-layered core-shell structured Al@TMs@AP composite fuels is provided. The relevant Al-based composite fuels are fabricated using spray granulation method and their morphologies are characterized by SEM and TEM techniques. The ignition and combustion of the solid propellants prepared with the core-shell structured composite fuels are evaluated and compared with that of reference propellant formulated with typical compositions using laser ignition setup and combustion diagnostic system. Results indicate that the heats of reaction measured for the Al@TMs@AP contained propellants are increased by as high as 13%, suggesting the completeness in combustion of Al is greatly improved by construction of Al composites with the multi-layered core-shell structure. The ignition delay times are apparently shortened from 421 ms to 373 ms for the propellants with Al@TMs@AP involved, which proves that the promoted ignition of Al is achieved by surface modification with transition metals. Additionally, the significantly increased burning velocity is monitored for the Al@TMs@AP contained propellants at low-pressure regime leading to the corresponding pressure exponents to be reduced by more than 20%, which is beneficial to the stability in operation of solid rocket motors. At last, the higher combustion wave temperature and finer particle size in CCPs are observed for the propellants containing surface modified Al, and the plausible combustion mechanism is proposed based on the phase composition analysis for the CCPs of studied propellants.

Multifunctional core-shell nanoparticles for temperature sensing and anti-counterfeiting

In this paper, the multi-functional multi-layer core-shell structure NaYF4: Ce3+/Eu3+@NaYF4 @NaYF4: Ho3+/Yb3+ nanoparticles (NPs) were prepared. These multi-layer NPs can be applied in temperature sensing with high relative sensitivity. Moreover, these NPs can be used in multimode optical anti-counterfeiting. Based on structure design and doped earth ions optimized, the maximum relative sensitivity is further promoted from 0.9 %·K−1 at 234 K (Eu/Ho) to 5.1 %·K−1 at 113 K (Ce/Eu@Y@Ho/Yb) by the blocking effect of the inter layer and by cross-relaxation of introducing Ce3+ and Yb3+ ions. Meanwhile, by introducing Ce3+ and Yb3+ ions, the NPs provide multimode emissions under multiple excitations, which are beneficial for the application of optical anti-counterfeiting. The NPs present increased sensitivity of temperature sensing and improved security of optical anti-counterfeiting, which has promising applications in biological cell calibration, micro-integrated circuits, etc.

A Multifunctional Nanocarrier System for Highly Efficient and Targeted Delivery of Ketamine to NMDAR Sites for Improved Treatment of Depression.

Ketamine (KA), commonly used as an anesthetic, is now widely studied as an antidepressant for the treatment of depression. However, due to its side effects, such as addiction and cognitive impairment, the dosage and frequency of (S)-ketamine approved by the FDA for the treatment of refractory depression is very low, which limits its efficacy. Here, a new multifunctional nanocarrier system (AC-RM@HA-MS) with specific targeting capabilities is developed to improve the efficacy of KA treatment. KA-loaded NPs (AC-RM@HA-MS-KA) are constructed with a multilayer core-shell structure. KA-loaded mesoporous silica NPs are prepared, conjugated with hyaluronic acid (HA) as pore gatekeepers, and sheathed with an RBC-membrane (RM) for camouflage. Finally, the surface is tagged with bifunctional peptides (Ang-2-Con-G, AC) to achieve specific targeting. One peptide (Ang-2) is acted as a guide to facilitate the crossing of the blood-brain barrier (BBB), while the other (Con-G) is functioned as a ligand for the targeted delivery of KA to the N-methyl-D-aspartate receptor sites. Animal experiments reveal that AC-RM@HA-MS-KA NPs effectively cross the BBB and directionally accumulate in the curing areas, thereby alleviating the depressive symptoms and improving the cognitive functions of depressed mice. After treatment, the depressed mice almost completely return to normal without obvious symptoms of addiction.

Ultra-responsive and selective ethanol and acetone sensor based on Ce-doped Co3O4 microspheres assembled by submicron spheres with multilayer core-shell structure

The sensitive detection of ethanol and acetone is of great significance to address environmental toxicity concerns. Herein, a novel Ce-doped Co3O4 microsphere is precisely fabricated and assembled by abundant submicron spheres with multilayer core-shell configuration employing metal-organic frameworks (MOFs) as template and PVP as the structure-directing agent, and the formation mechanism of the microspheres with hierarchical structure is explored. Moreover, the gas sensing performance of Ce-doped Co3O4 sensor are investigated toward ethanol and acetone. The sensor based on CoCe0.025-350 (the molar ratio of CeCo = 0.025) microspheres exhibits remarkable responsiveness toward ethanol and acetone at relatively low operating temperatures (180 and 200 °C, respectively) and excellent long-term durability. The excellent sensing properties are firstly ascribed to the existence of abundant active sites and surface defects induced by Ce doping, and secondly originated from the hierarchical structure which benefits the absorption, diffusion of the gases on the sensor surface. Furthermore, detection limits as low as 0.1 ppm are achieved by the CoCe0.025–350 sensor. The sensing dynamics of the sensors are also investigated. The versatile strategy report herein can be employed to construct other transition metal oxides with excellent gas sensing properties.

A multi-layer core-shell structure CoFe2O4@Fe3C@NiO composite with high broadband electromagnetic wave-absorption performance.

Enhancing the absorption strength of electromagnetic waves and broadening the absorption band are constant goals in designing and preparing absorbing materials. The use of composites has shown to be a very efficient method for acquiring broadband-absorbing materials, while the construction of a core-shell structure has demonstrated a significant enhancement in absorption capability. In this paper, the nanocomposite metal-organic framework (MOF) derivative CoFe2O3@C with a double core-shell structure and the nanocomposite MOF derivative CoFe2O4@Fe3C@NiO with a three-layered core-shell structure have been prepared using a chemical compound. The multi-layer structure provides more active sites for the multiple reflection and scattering of electromagnetic waves, effectively improving the attenuation capability. The effective absorption band (EAB) (reflection loss (RL) ≤ -5 dB) of both CoFe2O3@C and CoFe2O4@Fe3C@NiO are broadened compared to that of the ZIF-67 derivative. In particular, the minimum reflection loss (RLmin) of CoFe2O3@C was -52.7 dB at 13.3 GHz and 2.04 mm, and the EAB (RL ≤ -5 dB) is as wide as 9.35GHz. Compared with the ZIF-67 derivative, the EAB exhibits a twofold rise, accompanied by a corresponding thickness increase of just 0.24 mm. At a matched thickness of 2.2 mm, the EAB of CoFe2O4@Fe3C@NiO can even reach 11.9 GHz.

High-intensity first near-infrared emission through energy migration in multilayered upconversion nanoparticles.

The development of Tm3+ 807 nm first near-infrared (NIR-I, 700-1000 nm) emission with second near-infrared (NIR-II, 1000-1700 nm) excitation is urgently needed, due to its potential application in biomedicine. In this work, a range of NaErF4:Yb@NaYF4:Yb@NaYF4:Yb,Tm@NaYF4 multilayer core-shell structure upconversion nanoparticles (UCNPs) were successfully prepared by a co-precipitation method. The strongest UC emissions can be obtained by changing the concentration of Yb3+ in the core and the first shell, and the proposed UC process was discussed in detail. The analysis shows that high-intensity NIR-I emission (807 nm) from Tm3+ and visible light from Er3+ were achieved through the energy migration among Yb3+ and the energy back transfer from Yb3+ to Er3+ under 1532 nm excitation. Besides, compared to bilayer UCNPs, multilayer core-shell UCNPs display superior optical performance. The high-intensity NIR-I emission at 807 nm (Tm3+:3H4 → 3H6) under 1532 nm NIR-II excitation demonstrates huge advantages in bioimaging.

Fabrication of novel multilayer core-shell structured nanofibers network reinforced carbon matrix composites for bone tissue engineering

To further optimize the structure of bone tissue engineering composites, silicon nitride nanowires-pyrolytic carbon-hydroxyapatite-carbon matrix (Si3N4nws@PyCnls-HA-C) composites with multilayer core–shell structures are synthesized by chemical vapor deposition (CVD), pulsed electrodeposition (PED), and chemical vapor infiltration (CVI) methods. The microstructure, in-vitro bioactivity, and in-vivo histocompatibility of Si3N4nws@PyCnls-HA-C (SPHC) composites are evaluated. In-vitro, the SPHC exhibited a cell proliferation rate of 157.7% and demonstrated outstanding protein adsorption. In-vivo, the SPHC demonstrated excellent histocompatibility. Therefore, the SPHC composites can serve as an alternative suitable biomaterial for bone tissue engineering.

Influence of Ti3AlC2 addition on water vapor resistance of low‐carbon Al2O3–C refractories

AbstractAl2O3–C refractories are potential candidates for use in gasifiers, and they are Cr2O3‐free. However, the oxidation of the carbon species and ceramic phases within the high‐temperature water vapor environment may deteriorate the integrity of the working lining. Ti3AlC2 has been verified as an effective antioxidant for Al2O3–C refractories in air. In this study, the structural transformation of Ti3AlC2 during heat treatment and the water vapor resistance of Ti3AlC2‐containing Al2O3–C refractories are investigated. The results show that the oxidation of Ti3AlC2 and Si in the matrix contributes to the in situ formation of a multilayer core–shell structure of TiC–AlTi2O5–Al6Si2O13. These structural evolutions improve densification and stimulate pore size refinement, which enhances the mechanical properties and thermal stress resistance of the specimens. In particular, the refined pore size contributes to the significantly improved water vapor resistance at high temperatures.

D-Cysteine Functionalized Superhydrophobic Nanocomposite Coating with Multiple-Action Antibacterial Property and Enhanced Mechanical Durability

In this study, a durable superhydrophobic antibacterial coating was developed by a facile spraying method. A mixture of bisphenol A diglycidyl ether (BADGE) and hydrophobic SiO2 nanoparticles was sprayed on carbon steel to provide a superhydrophobic substrate. D-cysteine (D-cys) functionalized SiO2/dopamine/silver nanoparticles with multilayer core-shell structure were then sprayed on superhydrophobic substrate to enhance antibacterial performance. The results of morphology observation and X-ray photoelectron spectroscopy (XPS) indicated the successful preparation of antibacterial nanoparticles and presented the hierarchical micro/nanostructures of coating surface. The as-prepared coating exhibited superhydrophobicity, with the water contact angle of ~153°. The coating was endowed with good mechanical durability, which maintained the water contact angle of ~150° after 180 cycles in tape-peel tests. The results of electrochemical impedance spectroscopy showed satisfactory corrosion resistance of this coating during 3 days of immersion in 3.5% NaCl solution. Furthermore, the coating showed excellent antibacterial performances against Escherichia coli and Pseudomonas aeruginosa, which benefited from the synergistic actions of low wettability of superhydrophobic surface, bactericidal behavior of Ag nanoparticles, and biofilm inhibition effect of D-cys.

Study on improving the self-repairing effect of cement-based materials by microbial mineralization coupled with inorganic minerals

As a green and intelligent method, the self-repairing technology based on microbial mineralization had obvious defects. In this study, microbial mineralization coupled with inorganic minerals was used to realize the full-depth repair of cracks in cement-based materials, and the feasibility was systematically demonstrated. The self-repairing carrier with multilayer core-shell structure was prepared, and the average particle strength was 36.12 N; Protective layer was composed of hydrated calcium silicate, hydrated calcium aluminate and other hydration products, which had relatively dense structure. Compatibility between microorganisms and carrier was deeply studied, and the growth performance of microorganisms after long-term storage was basically equivalent to that of the initial microorganisms. Composition and microstructure of products in crack area were studied by X ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS), and products were mainly composed of calcium carbonate and ettringite with particle sizes of approximately 5–10 µm.The repair effect was studied by stereomicroscope, X ray computed tomography (X-CT) and ultrasonic detector. A large number of products were deposited on the two surfaces of the specimen, the crack was effectively filled; In addition, more products were deposited around the carrier, and a large number of cracks were repaired. Based on the above research, repair mechanism of the full-depth was identified. Microbial mineralization was mainly committed to the repair of crack surface, while ettringite prepared by inorganic reaction could repair the interior of crack, and the combination of the two paths could achieve the full-depth repair.