Core-shell Structure Research Articles

Fabrication of highly biocompatible SiO2@au-BSA nanoconjugates: Towards a promising thermal therapy route

SiO2@Au nanoshells have gained relevance in recent years, especially in biomedical areas, acting as thermal therapy agents due to their high capacity to absorb light and transform it into heat that increases the temperature of the medium. Therefore, it is important to develop methodological strategies to obtain stable, highly specific and biocompatible nanoparticles. In this work, the synthesis of core-shell structures based on SiO2@Au is reported, where the growth a thin shell ⁓ 46 nm on silica platform was possible. Subsequently, optimal conditions were developed for the binding of a bovine serum albumin (BSA) protein using a thiolated linker such as mercaptoethanol. Likewise, the photothermal conversion capacity was investigated using thermal lens spectroscopy. Thermal diffusivity values were reported for the first time during the conjugation process of gold nanoshells, where an increase of 37.5 % was recorded as the conjugation was completed. Finally, the cytotoxic potential of the developed nanoconjugates was evaluated through their hemolytic rate in human red blood cells. The findings suggest high hemocompatibility of the SiO2@Au-BSA complex because they did not cause significant oxidative stress and are classified as nonhemolytic. Therefore, in this work we propose a synthesis route for a thermal agent based on SiO2@Au and bovine serum albumin, highly biocompatible and with high photothermal conversion. The results of this work aim to clarify the safety of using gold nanoshells as a thermal therapy agent.

Synthesis and Characterization of Submicron Spherical Core-Shell High-Energy Composites via Electrospray Method

In this study, submicron spherical core-shell high-energy composites of RDX/F2311@CuO/Al were synthesized using the electrospray method. The results demonstrate that the combustion time of composite high-energy microspheres, prepared via electrospraying, was significantly reduced to 460.0 ms from an original 2296.0 ms observed in samples prepared by physical mixing. Additionally, the flame burning was more concentrated, and the combustion process exhibited greater stability. Additionally, the flame combustion exhibited greater concentration and the overall combustion process was more stable. Furthermore, by manipulating the proportion of non-energy-containing components, it is possible to obtain composites with adjustable combustion rates. By manipulating the ratio of aluminium thermal agent, it is possible to procure a composite material with a more vigorous combustion process, thereby enabling the functional modulation of said composite material. Compared to the raw material RDX, the H50 value of the composite microspheres has increased from 14.49cm to 25.16cm, indicating a significant enhancement in impact resistance along with a remarkable desensitization effect. Additionally, the explosion percentage of the composite microspheres has been reduced from 84% to 68%. These significant desensitization effects highlight the morphological advantages of the core-shell structure and the synergistic reaction energy benefits of the components involved.

Functional recycling of grain boundary diffusion processed Nd-Fe-B sintered magnets

Sintered Nd-Fe-B magnets industrially produced employing the grain boundary diffusion process (GBD) were recycled by the so-called functional or short-loop recycling approach, based on hydrogen decrepitation (HD). Microstructural and magnetic differences between the original and the recycled materials were analyzed. The functional recycling of GBD magnets leads to the dissolution of the core (heavy rare earth lean) - shell (heavy rare earth rich) structure through the different heat treatment steps which include hydrogen decrepitation, sintering, and annealing. The recycled magnets show similar rectangular demagnetization curves with squareness of 96 %, and only a slightly decreased remanence of 5 % to 1.31 T, but a larger decrease in coercivity of 21 % to 1703 kA/m. A new GBD step using 1.5 wt.% Tb with a pure Tb-foil as diffusion source leads again to the formation of a core-shell structure with 0.5 µm thick Tb-shells which is similar to the microstructure of the original magnets prior to recycling. The coercivity of the recycled magnets is increased by 35 % from 1315 kA/m to 1780 kA/m at 50°C and shows similar magnetic values as the original industrial magnets at 150°C and 200°C, respectively. The temperature coefficients for the remanence, α, and for the coercivity, β, can also be fully restored and even exceed the original values which leads to an improved temperature stability of the recycled magnets compared to the original magnets.

Fabrication of hollow Fe3O4 microspheres encapsulated by single-walled carbon nanohorns for high-performance microwave absorption

Due to the increasingly serious electromagnetic radiation and pollution problems, it is urgent to develop high-performance electromagnetic wave absorbing materials. Herein, the hollow Fe3O4 microspheres encapsulated by single-walled carbon nanohorns (H-Fe3O4@SWCNHs) have been synthesized via facile solvothermal approach. The obtained H-Fe3O4@SWCNHs composite exhibits a unique hollow core-shell structure and superior microwave absorption performance. When the matching thickness is 2.0 mm, the composite shows a minimum reflection loss value of −42.2 dB at 13.6 GHz and a maximum effective absorption broadband value of 6.2 GHz covering from 11.8 to 18 GHz. The excellent microwave absorption performance of the H-Fe3O4@SWCNHs composite is mainly attributed to the unique hollow core-shell structure, optimal impedance matching, and synergistic effects of dielectric loss and magnetic loss. Therefore, the present work provides a new kind of ideal microwave absorbing material with light weight, thin thickness, wide bandwidth and strong absorption capability for high-performance microwave absorption.

Versatile hybrid magnetic core silver-shell (Fe3O4@PEI@Ag) microspheres based SERS substrates for detection of organic dyes pollutant

In recent years, the development of highly sensitive and versatile substrates for Surface-Enhanced Raman Scattering (SERS) has become pivotal in environmental monitoring. This study introduces a hybrid SERS substrate designed to enhance the detection and discrimination of organic dyes in aqueous environments. In this report, we present silver shell magnetic core (Fe3O4@PEI@Ag) microspheres as a versatile SERS substrate for the detection and differentiation of organic dyes, specifically malachite green (MG), crystal violet (CV), Rhodamine 6G (R6G), and Safranin O (S.O), which are often overlooked water pollutants. The core-shell structure of Fe3O4@PEI@Ag microspheres have been synthesized via seed-mediated growth method. The microspheres, integrates a magnetic core of iron oxide (Fe3O4) through a polymeric layer of polyethyleneimine (PEI) with silver shell (Ag), are optimized to act as magnetic separator and show SERS activity. The SEM measurements confirm the spherical shape of grown nano-particles whereas magnetization experiments confirm the presence of magnetic cores as well non-magnetic layers coating in the end products. These microspheres with aluminium (Al) base combination demonstrate high SERS sensitivity with enhancement factor of 1 × 105, 5.6 × 106, 6.4 × 106, and 4.2 × 105 for MG, CV, R6G, and S.O respectively. The detection limits have been found in the range between 10–8–10–10 for all four dyes. A linear relationship between Raman intensity and concentrations of dyes make it suitable for quantitative analysis of unknown concentration. Principal component analysis (PCA), a multivariate analysis has been adopted to discrimination of dyes. These dyes have been effectively detected quantitative in tap water to express substrate's suitability in real-world application. Their dual functionality, as SERS-active substrate and as magnetic separator, enhances their utility in real-world applications such as organic contaminants in aquatic environments.

Hierarchical core-shell ZIF-11@ZIF-8 composite nanocatalyst for high-yield simultaneous transesterification-esterifications of sunflower oil to produce biodiesel

Decreasing the mass transfer resistance is a promising technique to prepare an efficient catalyst for improving biomass macromolecules conversion in biodiesel production. In this study, hierarchical core–shell composite nanocatalysts were prepared through a solvothermal technique using zeolitic imidazolate framework-8 (ZIF-8) and ZIF-11 metal–organic frameworks (MOFs). The nanocatalysts were characterized by XRD, FT-IR, BET, FE-SEM, EDS, XPS, TEM, NH3-TPD, and CO2-TPD analyses. The results showed high crystallinity, high surface area (1446.86 m2/g), high pore volume (0.65 cm3 g−1), and mesoscale pore size (2.37 nm). Furthermore, TEM images confirmed the formation of core–shell structure for the composites. The catalytic activity was evaluated in the transesterification of sunflower oil at different operating conditions. The highest biodiesel yield (96.4 %) and full free fatty acid (FFA) conversion were obtained over the ZIF-11@ZIF-8 nanocatalyst at the optimum operating conditions: 120 °C, catalyst concentration of 8 wt%, methanol to oil ratio of 40:1, and 10 h. The ZIF-11@ZIF-8 nanocatalyst showed high thermal and chemical stability after several sequence cycles, leading to high reusability.

Exploring Magnetic Disorder in Inverted Core-Shell Nanoparticles: The Role of Surface Anisotropy and Core/Shell Coupling.

In this work, we have studied the effect of internal coupling in magnetic nanoparticles with inverted core-shell structure (antiferromagnet-ferrimagnet) and also magnetic surface anisotropy, performing Monte Carlo simulations based on a micromagnetic model applied in the limit of lattice size equal to the crystalline unit cell. In the treatment, different internal regions of the particle were labeled in order to analyze the magnetic order and the degree of coupling between them. The results obtained are in agreement with experimental observations in CoO/CoFe2O4 and ZnO/CoFe2O systems, which we have taken as reference. It is observed that the surface anisotropy decreases the coercive field and the blocking temperature of the system. However, the core/shell coupling improves these properties and magnetically hardens the system. Our study shows that a significant magnetic stress is generated in the system, leading to magnetic disorder in the spins of the particle interface. On the other hand, in cases of high surface anisotropy, within a range of interfacial exchange values, a clear magnetic disorder is observed in the shell, which leads to anomalous behavior because the magnetization reversal process is no longer coherent.&#xD.

Preparation of Novel Hierarchical Catalysts by Simultaneous Generation of β-Zeolite and Mesoporous Silica for Catalytic Cracking.

The gel skeletal reinforcement (GSR) method was applied at the preparation stage of β-zeolite to prepare a novel hierarchical catalyst. A solution of hexamethyldisiloxane (HMDS) and acetic anhydride, a GSR reagent, was added to the mixture of colloidal silica, sodium aluminate, tetraethylammonium hydroxide, sodium hydroxide and water, and successive aging and hydrothermal treatment gave microporous β-zeolite surrounded by mesoporous silica like core-shell structure. Its properties were characterized by XRD, nitrogen adsorption and desorption, NH3-TPD, TEM, and TG-DTA measurements, and further characteristics of the catalysts produced were clarified by the catalytic cracking of n-dodecane. The hierarchical structure of microporous zeolite and mesoporous silica was shown from GSR-2.9HS-H-Beta to GSR-3.2HS-H-Beta, where the molar ratio of HMDS and silica source of β-zeolite was 2.9~3.2 : 100. It was found that in the catalytic cracking of n-dodecane, the relative activity (the conversion per the amount of zeolite crystals) increased with the increase in mesopore volume and surface area. The result indicated that the introduction of mesopores was effective even in catalytic cracking of small molecule of n-dodecane.

Core-shell structures assembled from magnetic covalent organic frameworks as a Ti4+-fixed affinity substrate for the identification of phosphopeptides in colorectal cancer serum.

When it comes to the early detection of colorectal cancer (CRC), the study of protein phosphorylation is crucial. This work used magnetic covalent organic framework (COF) materials as substrates. The magCOF@PM-Ti4+ composites were obtained by constructing the three-dimensional cross-linked structures and chelating them with Ti4+ in a green and economical way, which was utilized to identify the phosphopeptides. This material possesses magnetic properties that facilitate simplified experimental manipulation, has superior sensitivity (0.2 fmol), excellent selectivity (1000:1), and good reusability (10 cycles), and achieves outstanding recovery rates (103.4 ± 1.2%). In addition, magCOF@PM-Ti4+ was utilized to identify phosphopeptides in human serum. One hundred phosphopeptides were identified from three normal control serums, whereas 98 phosphopeptides were identified from three CRC serums. The results demonstrated that magCOF@PM-Ti4+ has great potential in efficiently identifying low-abundance phosphopeptides.

Upcycling of waste polyethylene terephthalate (PET) into CoFe@C for highly efficient PV-driven bifunctional seawater splitting via a “waste materialization” strategy

Developing green and efficient techniques to convert plastic wastes into functional materials is attractive and remains highly challenging. This study employs a hydrothermal combining with pyrolysis process for constructing a Co3Fe1@C heterostructure from the polyethylene terephthalate (PET) waste-mediated metal-organic frameworks. The as-obtained Co3Fe1@C shows a core-shell structure and possesses good performance towards water electrolysis. The Co3Fe1@C can attain the current density of 100 mA cm−2 with an overpotential of 250 mV for oxygen evolution reaction (OER). In addition, the bifunctional Co3Fe1@C can realize the overall seawater electrolysis at 50 mA cm−2 with good stability for 280 h driven by a 2.2 V commercial silicon solar cell. Overall, this study demonstrates a green chemistry approach to simultaneous plastic waste upcycling and cost-effective electrocatalyst fabrication, which may stimulate further research on the “waste materialization” approach to converting solid waste into highly efficient catalysts for various chemistry and energy industry applications.

Targeted Delivery of Celastrol by GA-Modified Liposomal Calcium Carbonate Nanoparticles to Enhance Antitumor Efficacy Against Breast Cancer

Background/Objectives: Breast cancer, a leading health threat affecting millions worldwide, requires effective therapeutic interventions. Celastrol (CEL), despite its antitumor potential, is limited by poor solubility and stability. This study aimed to enhance CEL’s efficacy by encapsulating it within glycyrrhizic acid (GA)-modified lipid calcium carbonate (LCC) nanoparticles for targeted breast cancer therapy. Methods: The 4T1 mouse breast cancer cells were used for the study. GA-LCC-CEL nanoparticles were prepared using a gas diffusion method and a thin-film dispersion method. GA-LCC-CEL were characterized using the zeta-potential, dynamic light scattering and transmission electron microscope (TEM). The in vitro release behavior of nanoparticles was assessed using the in vitro dialysis diffusion method. Cellular uptake was examined using flow cytometry and confocal microscopy. Intracellular ROS and Rhodamine 123 levels were observed under fluorescence microscopy. MTT and colony formation assays assessed cytotoxicity and proliferation, and apoptosis was analyzed by Annexin V-FITC/PI staining. Wound healing and transwell assays evaluated migration, and Western blotting confirmed protein expression changes related to apoptosis and migration. Results: GA-LCC-CEL nanoparticles displayed a well-defined core-shell structure with a uniform size distribution. They showed enhanced anti-proliferative and pro-apoptotic effects against 4T1 cells and significantly reduced breast cancer cell invasion and migration. Additionally, GA-LCC-CEL modulated epithelial-mesenchymal transition (EMT) protein expression, downregulating Snail and ZEB1, and upregulating E-cadherin. Conclusions: GA-LCC-CEL nanoparticles represent a promising targeted drug delivery approach for breast cancer, enhancing CEL’s antitumor efficacy and potentially inhibiting cancer progression by modulating EMT-related proteins.

Optimization and performance assessment of Ag@SiO2 core–shell nanofluids for spectral splitting PV/T system: Theoretical and experiment analysis

Ag@SiO2 nanofluid is widely used in spectral splitting PV/T system. Its core–shell structure has great influence on the optical properties. In this work, we focus on the comprehensive analysis and structure optimization of Ag@SiO2 nanofluid to achieve its optimal spectral performance. DDA method is used to predict the optical properties of Ag@SiO2 nanofluid and an optimization model based on filter efficiency is proposed. The effect of the SiO2 shell thickness and Ag core mass concentration is analyzed. It indicates that the spectral performance of Ag@SiO2 nanofluid can be improved with SiO2 shell thickness of 15–40 nm and Ag core mass concentration of 81–135 mg/L. To achieve the same theoretical merit function of 1.46, the usage of Ag mass can be reduced by 25/33/44/62 % with SiO2 coating of 10/20/40/70 nm. The optimal structure to achieve the highest filter efficiency η of 37.8 % is with a shell thickness of 20 nm and a mass concentration of 113.9 mg/L. An indoor PV/T operation testing is conducted to verify the optimization results. The merit function of Ag-based nanofluids increases from 1.58 to 1.598 and a reduction in Ag usage of 17 % is achieved with a SiO2 coating shell of 17.8 nm. Operation stability is also enhanced with no aggregation observed during the working cycle and 7-day static experiment.

High-Yield Production of SiV-Doped Nanodiamonds for Spectroscopy and Sensing Applications.

Nanodiamonds (NDs) containing optically active centers have gained significant relevance as the material of choice for biological, optoelectronic, and quantum applications. However, current production methods lag behind their real needs. This study introduces two CVD-based approaches for fabricating NDs with optically active silicon-vacancy (SiV) color centers: bottom-up (BU) and top-down (TD) methods. The BU approach generates nanoporous diamond films with a core-shell structure, while the TD method employs molten-salt thermal etching to create uniform porous structures from nanocrystalline diamond films. Comprehensive characterization using advanced techniques revealed distinct morphologies and optical properties for each approach. The BU method yielded higher-quality diamond phases with top-surface incorporation of SiV centers, while the TD method demonstrated efficient nondiamond phase removal. Ultrasonic disintegration of both porous films produced NDs ranging from 40 to 500 nm, with unique morphologies characteristic of each approach. Photoluminescence measurements confirmed SiV centers (738 nm) in all NDs, exhibiting sensitivity to surface terminations, particularly in BU samples. Temperature-resolved spectroscopy shows the potential of the fabricated NDs for nano thermometry over a wide range of temperatures up to 100 °C. The zero-phonon line shows 0.022 ± 0.003 nm/K sensitivity, while the line width exhibits 0.068 ± 0.004 nm/K broadening. The presented BU and TD methods offer significant advantages over existing techniques, including streamlined production processes, high-yield ND synthesis with tailored properties, and the potential for scalable, cost-effective manufacturing.

Epitaxial Growth of Multicolor Lanthanide MOFs by Ultrasound for Photonic Barcodes.

Epitaxially grown lanthanide metal-organic frameworks (Ln MOFs) exhibit multicolor and characteristic Ln emission with sharp emission bands, which are of great value in the field of information security and anti-counterfeiting. Epitaxial growth of Ln MOFs is generally achieved by solvothermal or hydrothermal methods, which suffer from challenges such as high reaction temperature and long growth time. Here, we report the fast epitaxial growth of multicolor lanthanide MOFs by an ultrasonic method at room temperature. The TbSmSQ shows a core-shell type structure with the Tb ion in the core and Sm in the shell within one crystal and exhibits the characteristic emission lines of Tb and Sm, respectively. The nonporous structure and large distance between lanthanide ions effectively avoid the influence of solvent vapor on the intensity and color of luminescence emission. Its application as photonic barcodes has been studied. This work demonstrates the feasibility of epitaxial growth of multicolor Ln MOFs by the ultrasonic method and its value for anti-counterfeiting and information security applications.

The Design of Ternary Nanofibers with Core–Shell Structure for Electromagnetic Stealthy Antenna

The Design of Ternary Nanofibers with Core–Shell Structure for Electromagnetic Stealthy Antenna

Fabrication of hydrogel mini-capsules as carrier systems

Conventional drug administration often results in systemic action, thus needing high dosages and leading to potentially pronounced side effects. Targeted delivery, employing carriers like nanoparticles, aims to release drugs at a target site, but only a small fraction of nanoparticles actually reaches it. Microrobots have been proposed to overcome this issue since they can be guided to hard-to-reach sites and locally deliver payloads. To enhance their functionality, we propose microrobots made as deformable capsules with hydrogel shells and aqueous cores, having the potential added advantages of biocompatibility, permeability, and stimulus-responsiveness. Endowing microrobots with deformability could allow them to navigate inside capillaries and cross barriers to finally reach the target site. In this study, we present a cost-effective method for fabricating core-shell structures without the use of organic solvents, surfactants, or extreme pH conditions unlike other techniques (e.g. Layer by Layer). The process begins with the dripping of a mixture of hydrogels, agarose and alginate, into a solution to gelate the drops into beads. After they are loaded with calcium ions at different concentrations, they are immersed in an alginate solution to form the shell. Finally, the beads are heated to let the agarose melt and diffuse out, leaving a liquid core. By varying the concentration of calcium ions, we obtain shells of different thicknesses. To estimate it, we have developed a method using the colour intensity from microscope images. This allowed us to observe that lowering the calcium ions concentration below a threshold does not lead to the formation of continuous shells. For higher concentrations, although the core may remain partially gelled, continuous shells successfully form. Therefore, our fabrication process could find applications in drug delivery, encapsulation systems, and microrobotics.

Biobased amphoteric aerogel with core-shell structure for the hierarchically efficient adsorption of anionic and cationic dyes

Efficient and simultaneous removal of anionic and cationic dyes from wastewater using low-cost and environmentally-friendly adsorbent is highly required. Herein, the carboxylated cellulose (carboxyl content: 2.97 mmol/g) derived from pomelo peel was extracted by a one-step H2O2/H2SO4-mediated oxidation method. Subsequently, a novel pomelo-peel cellulose/chitosan/sodium alginate (PCS) amphoteric aerogel with a specific core-shell structure was synthesized by multiple physical cross-linking strategies. The shell layer and core layer of the optimized P3CS0.75 aerogel can selectively adsorb cationic dyes and anionic dyes, in which, the theoretical maximum adsorption capacities were 888.27 mg/g and 1816.87 mg/g towards methylene blue (MB) and Congo red (CR), respectively. Especially, the aerogel’s core/shell layer exhibited hierarchical adsorption behavior without overlapping sites even in the binary dye systems. The adsorption performance of obtained amphoteric aerogel remained effective in a wide pH range and under different practical water systems. Moreover, the removal efficiencies for MB and CR were slightly reduced from 90.76 % and 99.66 % to 88.08 % and 91.39 %, respectively, after 5 adsorption-desorption cycles, and the aerogel’s structural integrity was also maintained due to its good compressive strength (487.16 KPa). In addition, the adsorption mechanism of PCS aerogel was investigated using adsorption kinetics, isotherm, thermodynamics, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy. It was proved that the adsorption process was endothermic spontaneous-monolayer adsorption driven by electrostatic attraction and hydrogen bonding. Therefore, the prepared biobased aerogel was expected to be a prospective material for removing mixed dyes from wastewater.

Improving the Electrocatalytic Activity of a Core/Shell NiCo-ZIF@PBA Catalyst by Co-O-Fe Bridge Bonds for Water Oxidation.

In response to the limitations of slow reaction kinetics and elevated overpotentials in the OER, a novel core-shell structured electrocatalyst, termed NiCo-ZIF-67@Fe-Co-Ni-PBA or NiCo-ZIF@PBA, has been developed. This material demonstrates exceptional catalytic performance, exhibiting a minimal overpotential of approximately 188 mV at 10 mA cm-2, alongside a Tafel slope of 109 mV dec-1. Its robust stability in a 1 M KOH solution during the OER operations is noteworthy. Theoretical insights from DFT calculations reveal that a Co-O-Fe bridging configuration within NiCo-ZIF@PBA lowers the energy barrier for the reaction to 1.79 eV, a significant reduction from 2.67 eV observed with NiCo-ZIF-67. The improvement in electrochemical performance is primarily due to the emergence of Co3+ ions, which results from the efficient charge transfer occurring at the interface of the PBA and NiCo-ZIF core-shell structure. These findings suggest a promising strategy for designing advanced core-shell materials for electrocatalytic applications.

Coupling Effect of Elemental Carbon and Organic Carbon on the Changes of Optical Properties and Oxidative Potential of Soot Particles under Visible Light.

Soot particles, coming from the incomplete combustion of fossil or biomass fuels, feature a core-shell structure with inner elemental carbon (EC) and outer organic carbon (OC). Both EC and OC are known to be photoactive under solar radiation. However, research on their coupling effect during photochemical aging remains limited. This study examines how the optical properties and oxidative potential (OP) of wood, coal, and diesel soot particles with varying EC and OC levels are affected by exposure to visible light. Wood soot, which has the highest OC content, showed the most significant changes in both optical properties and OP, indicating its highest sensitivity to visible light aging. Molecular composition analysis revealed that the reduction of polycyclic aromatic hydrocarbons (PAHs) and methyl-PAHs primarily affects the optical properties, while oxygenated PAHs play a major role in OP. Combined with the results from reactive oxygen species detection, it is suggested that EC initiates photoreactions by generating superoxide anions, while OC undergoes compositional changes that result in subsequent atmospheric effects. These findings enhance our understanding of the photochemical aging process of soot particles and their implications for climate and health.

Tribological and Corrosion Properties of Al2O3@Y2O3-Reinforced Ni60A Composite Coatings Deposited Using Laser Cladding

Since rare earth oxides and hard ceramic particles improve coating quality, a novel Al2O3@Y2O3 core–shell structure was prepared. Then, Ni60A coatings with different amounts (2~6 wt.%) of Al2O3@Y2O3 core–shell structures were prepared using laser cladding technology on an H13 steel surface. To demonstrate the unique effect of the core–shell structure on the performance of the coatings, a set of controlled experiments was also conducted with different proportions of Al2O3-Y2O3 mechanically mixed powders. The effect of Al2O3@Y2O3 addition on the phase composition, element distribution, microstructure, wear, and corrosion resistance of the coatings was characterized and tested thoroughly. By comparing the forming quality, hardness, wear, and corrosion resistance of the different coatings, 2 wt.% was confirmed as the optimal concentration of Al2O3@Y2O3, and its corresponding friction coefficient was about 0.44. The wear rate was approximately 4.15 × 10−3 mm3·(N·m)−1, the self-corrosion potential was around −0.3659 V, and the self-corrosion current density was about 1.248 × 10−6 A·cm−2.