8594results about "Material nanotechnology" patented technology

The invention relates to an iridium dioxide catalyst and a preparation method and application thereof, the iridium dioxide catalyst is a material with a three-dimensional porous structure, and the three-dimensional porous structure comprises mesopores and macropores; the characteristic peak of rutile type iridium dioxide exists in the XRD spectrogram of the iridium dioxide catalyst. When the catalyst disclosed by the invention is used as an anode catalyst in water electrolysis hydrogen production, the loading capacity of the catalyst can be effectively reduced, the dispersity is improved, and meanwhile, the catalyst has better mass transfer effect and conductivity, higher catalytic activity and excellent stability.

The invention discloses a self-energy-supply multi-mode sensing electronic skin based on ionic gel heterojunction array integration and a preparation method and application of the self-energy-supply multi-mode sensing electronic skin. The electronic skin adopts a multi-layer composite structure design and comprises an electrode array layer, a silver paste connecting layer, a nano material doped ionic gel array layer and a pure ionic gel continuous layer, and passive self-energized work is realized through a space ion migration effect at a heterogeneous gel interface. The method is characterized in that the design of a multi-layer flexible composite structure is adopted, space-time coded light, temperature, pressure and humidity four-mode stimulation can be synchronously converted into electroneurographic signals, and a collaborative identification strategy of response intensity dynamic range and synaptic learning / delay time difference is utilized; and high-precision decoupling of the multi-source signals is realized in combination with a classification decision tree algorithm. The electronic skin has the characteristics of flexibility, deformation, environment self-repairing and bionic synapse, and geometrical characteristics of a reconfigurable target source are fused through time-space domain multi-modal data.

The invention relates to a carbon quantum dot for strengthening and promoting growth of microalgae and application thereof. In the process of preparing the carbon quantum dots by a conventional hydrothermal method, a precursor mixture is subjected to acidification modification in advance, the pH value is adjusted to 2 by using nitric acid, and then a hydrothermal reaction is performed, so that the prepared carbon quantum dots have the capability of promoting the growth of microalgae. However, if other acids are adopted or pH adjustment is not in place, the effect cannot be achieved, and even the inhibition effect can be achieved. The obtained product is good in effect and stable in performance, no special reaction device needs to be additionally arranged in the acidification modification process, and the method has the advantages that operation is easy and convenient, raw materials are easy to obtain, and the process can be quantified; the method is simple and convenient in process operation, has universality and is easy for industrial production.

The invention relates to the technical field of proton exchange membrane fuel cell cathode catalysts, and discloses a nanoscale high-entropy intermetallic compound catalyst and a preparation method and application thereof. According to the nanoscale high-entropy intermetallic compound catalyst, a nitrogen-doped porous carbon material derived from zeolite imidazole skeleton-8 is taken as a carrier, and the metal elements of a high-entropy intermetallic compound comprise platinum, copper, cobalt, nickel and iron or platinum, ruthenium, copper, cobalt, nickel and iron. The preparation method of the catalyst comprises the following steps: step 1, preparing a zeolite imidazole framework 8; 2, preparing and purifying a nitrogen-doped porous carbon material carrier; step 3, loading a metal precursor; and 4, preparing the nano-scale high-entropy intermetallic compound catalyst. Nanoscale, high dispersity and structure ordering of the high-entropy intermetallic compound are achieved, the high-entropy intermetallic compound serves as a PEMFC cathode catalyst, the ORR quality activity and durability can be remarkably improved, and Pt loading capacity and cost are effectively reduced.

The invention discloses a dry-process high-temperature-resistant lithium battery diaphragm and a preparation method thereof, and relates to the technical field of lithium battery diaphragms. The specific preparation method comprises the following steps: activating and cross-linking polypropylene, polyimide, a PP-b-PI block copolymer and a cross-linking agent BIBP under the protection of nitrogen to prepare a polypropylene-polyimide matrix; after melting, adding a pre-sintered ZrO2-coated Al2O3 core-shell filler, hydroxylated boron nitride and zinc borate, and carrying out double-stage screw extrusion, ultrasonic orientation, nitrogen annealing and cold roller quenching to obtain a mixed melt; carrying out warm stretching and hot air circulation heat treatment to prepare a hard elastic crystal base film; carrying out stretching, thermal relaxation and thermal shaping to obtain a microporous base membrane; after slitting, plasma activation is carried out, epoxy silane and tetraethyl orthosilicate / polybenzimidazole aerogel precursors are sprayed, and a nano closed-pore coating is formed through pre-curing and heat shrinkage curing; and finally eliminating static electricity and rolling to obtain a finished product. The lithium battery diaphragm prepared by the invention is excellent in high temperature resistance and low in thermal shrinkage rate.

The invention discloses a silicon-carbon negative electrode material, a preparation method thereof and a lithium ion battery, and relates to the technical field of lithium ion battery negative electrode materials. The material sequentially comprises a porous silicon core, a transition layer and a shell from inside to outside, the transition layer is a nitrogen-doped SiC / C composite layer, the shell comprises a graphene / carbon nanotube skeleton and MXene quantum dots, the MXene quantum dots are embedded in the graphene / carbon nanotube skeleton, boric acid ester bonds exist between carbon nanotubes and graphene, and the MXene quantum dots are embedded in the graphene / carbon nanotube skeleton. The silicon-carbon negative electrode material is based on dual-network dynamic bonding and stress gradient regulation and control, the cycle performance of the material can be remarkably improved, and the service life of the material can be remarkably prolonged.

The invention provides a phenolic resin-based spherical silicon-carbon composite material as well as a preparation method and application thereof, and belongs to the technical field of lithium battery materials. The preparation method comprises the following steps: preparing spherical phenolic resin by adopting a suspension polymerization method, curing to obtain phenolic resin microspheres, preparing porous carbon spheres by taking the phenolic resin microspheres as a carbon precursor in a carbonization and alkali activation manner, carrying out CVD vapor deposition on nano silicon, and carrying out carbon coating to obtain the phenolic resin-based spherical silicon-carbon composite material. The phenolic resin is utilized to form a highly cross-linked network structure after curing, the carbon spheres obtained after carbonization have good mechanical strength and rigidity, the porous structure of the porous carbon spheres provides a volume change buffering structure for nano-silicon, the lithium ion path is shortened, the spherical structure is beneficial to uniform dispersion, nano-silicon particles are prevented from gathering, and the performance of the lithium ion battery is improved. And the porous carbon spheres with high specific surface area can also improve the interface reaction activity, so that the problems of high volume expansion, low conductivity and slow ion diffusivity of silicon are solved.

The invention provides embedded metal fullerene and a preparation method thereof. The preparation method comprises the following steps: mixing a metal source and graphite powder, and filling a hollow graphite rod with the mixture to prepare an anode; the electrode is installed at the anode end of an electric arc furnace, and on-line activation is conducted through anode and cathode short-circuit current under the inert atmosphere; then carrying out arc discharge under specific air pressure and current, and collecting generated carbon ash; performing ultrasonic extraction by using an organic solvent to obtain a fullerene crude extracting solution; and finally, performing multi-stage separation and purification by high performance liquid chromatography, and performing primary and fine separation by sequentially adopting preparative and semi-preparative chromatographic columns to obtain a high-purity product. According to the method, a complete technical path capable of efficiently and controllably preparing the ultra-high-purity embedded metal fullerene is formed through a synthesis process integrating online activation and accurate atmosphere regulation and control and a multi-stage gradient chromatography purification strategy, and a solid foundation is laid for application of atomic-scale accurate materials in the frontier fields of quantum devices and the like.

This invention provides a transdermal nanoparticle delivery system for skin anti-inflammation, comprising a protein-blue calyx methyl ether-polymer shell capsule composite structure. The protein has an affinity for the skin, blue calyx methyl ether is loaded within the protein, and the polymer layer coats the surface of the protein. The blue calyx methyl ether nanoparticle transdermal delivery system has a size of 30-80 nm, and the polymer shell thickness is 10-35 nm. The surface properties of the polymer shell can be controlled according to the required transdermal delivery depth, enabling the protein to penetrate the skin barrier and be efficiently delivered deep into the skin, where the blue calyx methyl ether is then slowly released, targeting and alleviating skin inflammation. This addresses the drawback of low therapeutic efficacy of blue calyx methyl ether in treating skin inflammation due to unsatisfactory transdermal effects.

The invention relates to an electrolyzed water catalyst and a preparation method and application thereof, the electrolyzed water catalyst is a three-dimensional porous material of elemental iridium and / or iridium oxide, the specific surface area of the electrolyzed water catalyst is greater than or equal to 65 m < 2 > / g, the porosity is greater than or equal to 40%, and the electrolyzed water catalyst has a mesoporous and macroporous structure. The electrolyzed water catalyst disclosed by the invention has a large specific surface area, high porosity and a three-dimensional porous structure of mesopores and macropores, so that the electrolyzed water catalyst has better mass transfer performance and apparent catalytic activity. The three-dimensional porous structure of the catalyst can improve the utilization rate of the iridium element, so that the loading amount of iridium in a membrane electrode is reduced, and the catalyst has excellent stability. The preparation method provided by the invention is simple and convenient, and has relatively high economical efficiency.

The invention relates to a preparation method and application of a carbon dot-based nano enzyme. The preparation method of the carbon dot-based nano-enzyme comprises the following steps: taking sucralose and B vitamins as raw materials, and preparing the carbon dot-based nano-enzyme through a one-pot hydrothermal method. The preparation method of the carbon dot-based nano-enzyme provided by the invention is simpler in catalytic condition and higher in safety. The carbon dot-based nano-enzyme prepared by the invention has the advantages of high oxidase-like activity, low drug resistance, high biocompatibility and the like, can inhibit multi-drug-resistant bacteria, and can be applied to the aspects of aquatic product preservation and the like.

A copper-aluminum composite plate material prepared by aluminum liquid continuous casting and a process thereof. The method includes: S1, heating an aluminum ingot to 700-800° C. and smelting for 1-3 h; S2, degassing smelted aluminum liquid, and keeping the temperature and standing; S3, texturing a copper strip, and then cleaning; S4, heating the pretreated copper strip to 200-650° C.; S5, under the protection of inert gas, continuously casting the treated aluminum liquid on the treated copper strip, performing quenching crystallization on a copper-aluminum composite material, and performing oxygen-free continuous casting; and S6, continuous rolling: rolling the continuously cast copper-aluminum composite material to obtain the copper-aluminum composite plate material prepared by aluminum liquid continuous casting.

Microparticles for detecting biological materials are provided. Each of the microparticles includes: a core-shell structured microparticle consisting of a core including a magnetically responsive metal and a shell layer surrounding the core and having a uniform thickness; and capture probes introduced onto the shell layer to capture biological materials.

The invention relates to 500MPa-grade preheating-free welding structural steel and a preparation method thereof, belongs to the technical field of structural steel, and solves the problems that in the prior art, traditional structural steel is poor in welding performance, high in carbon equivalent, high in cold crack sensitivity and difficult to consider both high strength and good plasticity. The structural steel comprises the following chemical components in percentage by weight: less than 0.002% of C, less than 0.02% of Si, less than 0.03% of Mn, 1.5-2.0% of Ni, 1.5-2.0% of Cu, less than 0.0008% of S, less than 0.006% of P and the balance of Fe and inevitable impurities, wherein the carbon equivalent Ceq is less than or equal to 0.27. The combination of high strength (the yield strength is larger than or equal to 550 MPa, and the tensile strength is larger than or equal to 650 MPa), excellent welding performance (Pcm is smaller than or equal to 0.14), good plasticity (the percentage elongation after fracture is larger than or equal to 25%, and excellent low-temperature toughness (the impact energy at the temperature of-20 DEG C is larger than or equal to 200 J) is achieved, and the steel is suitable for the structural fields of ships, bridges, buildings and the like with strict requirements for welding performance and mechanical performance.

The invention relates to a textured KCu7S4 thermoelectric material and a preparation method thereof, and the method comprises the steps: sequentially adding a prepared KOH aqueous solution, CuCl2. 2H2O and Na2S. 9H2O into a high-pressure kettle, and fully stirring for dissolving; dropwise adding an N2H4.H2O aqueous solution into the mixed solution, fully stirring, sealing, transferring to a microwave chemical synthesis instrument, heating, keeping stirring, and reacting at a target temperature and self-generated pressure to generate a KCu7S4 nanowire preferentially growing along a [001] crystal orientation; and after the reaction is finished and natural cooling is carried out, a product is collected through centrifugation, full cleaning and vacuum drying are carried out, and then the KCu7S4 thermoelectric material with [001] preferred orientation in the direction perpendicular to the pressure direction is obtained through spark plasma sintering. According to the method, a surfactant and an organic solvent are not used, and macro, rapid, efficient and controllable preparation of the KCu7S4 nanowire is realized through a low-temperature, low-cost and low-energy-consumption microwave-assisted hydrothermal process.

An iridium-based catalyst. Relative to the total mass of the catalyst, the mass percentage content of an iridium element is 70% or higher. The apparent density of the catalyst is not higher than 0.55 g / cm3. The catalyst has a large specific surface area, high porosity and low apparent density, and therefore has excellent mass transfer performance and apparent catalytic activity. A three-dimensional porous structure of the catalyst can improve the utilization rate of the iridium element, thereby reducing the loading of iridium in a membrane electrode, and the catalyst has excellent stability. A preparation method provided is simple and convenient, and has relatively high economic efficiency.

The invention provides a sulfide solid electrolyte and a preparation method and application thereof, and relates to the technical field of lithium ion batteries. The preparation method comprises the following steps: S1, carrying out dry ball milling treatment on raw materials Li2S, P2S5 and LiX according to a required stoichiometric ratio, so that the raw materials are amorphized; s2, adding a solvent into the non-crystallized raw material obtained in the step S1, and carrying out wet ball-milling treatment to obtain a precursor with the particle size of 0.05-0.5 mu m; s3, the solvent is removed from the precursor slurry, the sulfide solid electrolyte is obtained through solid-phase sintering, all the steps are carried out in an inert atmosphere, and X is a halogen element. According to the present invention, the non-crystallization of the raw material is achieved through the dry ball milling, the uniform precursor slurry with the small particle size is obtained by combining the wet ball milling, and the sub-micron / nano-scale pure phase electrolyte material can be obtained after the sintering treatment, such that the electrode / electrolyte interface contact is improved, the impedance is reduced, and the battery performance is significantly improved.

The application discloses a MnFe2O4 / GO wave-absorbing aerogel with a directional aperture structure and a preparation method thereof, belongs to the technical field of wave-absorbing material preparation, and is characterized in that manganese ferrite (MnFe2O4) magnetic particles are uniformly loaded on the surface of graphene to obtain a graphene aerogel with a three-dimensional loose porous structure and magnetic particle assembly; the MnFe2O4 is prepared by using a low-temperature co-precipitation method, and the MnFe2O4 / GO wave-absorbing aerogel is prepared by combining directional freezing and heat treatment, and the method is mild and simple. The application improves the impedance mismatch problem of the graphene material, enhances the magnetic loss of the material, and obtains a novel porous aerogel wave-absorbing material which has both dielectric loss and magnetic loss by introducing the manganese ferrite.

The invention belongs to the field of carbon nanomaterials, and provides a method for preparing a carbon quantum dot material doped with elements such as silicon and aluminum by oxidative depolymerization and stripping of coal gangue. Comprising the steps of screening and matching of coal gangue, oxidative depolymerization stripping, centrifugal dialysis membrane filtration and modification, drying and the like, raw materials and all the steps are specifically set, and the particle size or fluorescence performance of fluorescent carbon dots can be specifically selected and set according to selective oxidative depolymerization stripping conditions. The main particle size of the prepared multi-inorganic-element doped carbon quantum dot material is kept within the range of 1.5-2.0 nm, the structure is stable, the optical performance also meets the requirements, and the material can be further modified and is expected to be applied to the fields of photovoltaic equipment, biological imaging, photocatalytic degradation of organic pollutants or sensing and the like.

The invention belongs to the technical field of lithium ion batteries, and particularly relates to a preparation method of a graded ordered silicon-carbon negative electrode material for a lithium ion battery, which comprises the following steps: (S1) mixing phenolic resin and a template agent, calcining, and etching to obtain porous carbon containing macropores; (S2) carrying out cracking and carbon coating on the silicon source gas to obtain nano crystalline silicon containing a carbon coating layer; (S3) mixing the porous carbon with the nano crystalline silicon containing the carbon coating layer, and then carrying out ultrasonic vibration, so that macropores of the porous carbon are filled with the nano crystalline silicon to obtain a silicon-carbon composite material I; (S4) treating the silicon-carbon composite material I by using a carbon-containing sealing agent, and then activating to obtain a silicon-carbon composite material II; and (S5) carrying out vapor phase silicon deposition on the silicon-carbon composite material II to fill the amorphous silicon in the pores of the porous carbon, and then carrying out carbon coating to obtain the graded ordered silicon-carbon negative electrode material. The silicon-carbon negative electrode material prepared by the invention is of a composite structure in which crystalline silicon and amorphous silicon are spatially and orderly distributed, so that the structural stability and the uniform distribution of silicon are realized.

The invention discloses a preparation method of a lithium iron phosphate positive electrode material, three iron sources with different forms and different particle sizes participate in preparation of the lithium iron phosphate positive electrode material, and gradation is formed to improve the compaction density and rate capability of the material. The EDTMPA reduces the viscosity of the slurry, is anchored on the surface of FePO4 particles through strong adsorption, inhibits particle aggregation through steric hindrance and electrostatic repulsion effect, and introduces hydrophilic groups to enhance wettability, reduce the viscosity of the system, optimize dispersion stability, accelerate particle crushing and refining, reduce the particle size and shorten the grinding time; in the sintering process, a reducing agent is generated through pyrolysis to inhibit too fast oxalic acid decomposition to cooperate with the generated reducing gas, Fe < 3 + > is completely reduced, the reduction temperature is reduced to inhibit grain growth, and the grading effect between large and small particles is improved; in addition, an N-doped carbon coating layer is formed through high-temperature cracking, pores are filled with residual carbon generated through decomposition of ferrous oxalate, the coating density is improved, the carbon-coated graphitization degree is improved, and then the electronic conductivity and the rate capability of the material are improved.

The invention relates to a metallized microbubble and a preparation method thereof, a construction method of a multifunctional composite probe, and a rapid bacterium capturing and sterilizing method, and belongs to the technical field of functional material preparation. The method aims at solving the technical problems that in the prior art, a metal coating on the surface of the hollow glass microbubble is not uniform, combination is not firm, and stability is poor. According to the technical scheme, the method is characterized by comprising the following steps: mixing surface-activated hollow glass microbubbles with a polyethyleneimine solution for reaction, and washing and drying to obtain polyethyleneimine-coated hollow glass microbubbles; then reacting with a single-stranded DNA buffer solution to obtain an intermediate product loaded with DNA; then introducing a silver nitrate solution to load silver ions on the surface of the compound; and finally, reducing through a sodium borohydride solution to prepare the metallized microbubbles. The metalized microbubbles prepared by the method can be used for constructing a multifunctional composite probe to realize efficient capture and synergistic antibiosis of targets such as bacteria.

The invention discloses a fuel cell cathode catalyst and a preparation method thereof, and belongs to the technical field of fuel cells. The preparation method of the fuel cell cathode catalyst comprises the following steps: adding a modified multi-walled carbon nanotube into a chloroplatinic acid aqueous solution with the mass concentration of 5g / L, carrying out ultrasonic treatment at 30-50 DEG C for 1-2 hours, and then carrying out freeze drying; and putting the dry powder into a horizontal tube furnace, introducing inert gas as protective gas, heating to 450-500 DEG C, preserving heat for 1 hour, cooling to room temperature along with the furnace, and taking out to obtain the fuel cell cathode catalyst. The modified multi-walled carbon nanotube is MWCNT / PEI / 5-formyl-2-thiopheneboronic acid, and the 5-formyl-2-thiopheneboronic acid is grafted after the PEI is grafted on the surface of the MWCNT, so that the dispersity of the MWCNT can be obviously improved, the agglomeration phenomenon of the MWCNT is reduced, the dispersion is more uniform, the loading capacity of platinum is high, the electrocatalytic activity of the catalyst is obviously enhanced, and the dosage of platinum is reduced.

The present invention generally relates to a process for synthesizing a graphene oxide quantum dots-iron phthalocyanine (FePc-GOQDs) nanocomposite with enhanced electrochemical properties, particularly for oxygen reduction reactions (ORR). The process begins by dispersing 500 mg of graphene oxide (GO) in a hydrogen peroxide and deionized water solution in a 1:10 volume ratio, followed by hydrothermal treatment at 180° C. for 8 hours to produce GO quantum dots (GOQDs). The resulting material is freeze-dried to obtain GOQDs powder. Subsequently, 60 mg of GOQDs are combined with 10 mg of iron phthalocyanine (FePc) and 20 mL of dimethyl sulfoxide (DMSO), and the mixture is subjected to microwave irradiation at 500 W and 150° C. for 30 minutes. The resulting composite is rinsed repeatedly with deionized water and ethanol, then dried at 120° C. to yield the FePc-GOQDs nanocomposite. This composite demonstrates superior ORR performance due to strong Fe—O bonding and optimized electronic interactions.

An imaging lens assembly module, which defines an optical axis, includes an optical element. The optical element includes a light blocking portion and an anti-reflecting thin film. The light blocking portion is opaque, and the light blocking portion is closer to the optical axis than the other portion of the optical element to the optical axis. The anti-reflecting thin film is disposed at least on a surface of the light blocking portion, and the anti-reflecting thin film includes a nano structure layer and at least one intermediate layer. The nano structure layer has a plurality of ridge-like protrusions which extends non-directionally. The intermediate layer is disposed between the nano structure layer and the optical element.

The invention relates to the field of optical elements, in particular to a coating method of a high-precision intense laser optical lens. The film coating method comprises the following steps: step 1, substrate pretreatment; step 2, surface activation; 3, a preparation stage; step 4, coating treatment; and step 5, post-processing. According to the method disclosed by the invention, the problems of adhesive force, uniformity, damage resistance and the like of a traditional method in strong laser lens coating are solved through fusion of double-plasma cooperation and a self-adaptive gradient composite coating technology. The method provided by the invention can be used for customized production for different laser scenes, and is suitable for high-end fields such as high-energy laser industry, quantum calculation, infrared imaging and the like.

The invention relates to an iridium-based catalyst, a preparation method thereof and application of the iridium-based catalyst in proton exchange membrane water electrolysis hydrogen production, the iridium-based catalyst is a material with a three-dimensional porous structure, and the iridium-based catalyst contains more than 80% by mass of iridium element; a characteristic peak of elemental iridium exists in an XRD spectrogram of the iridium-based catalyst. Compared with an existing iridium black catalyst, when the iridium-based catalyst disclosed by the invention is used for producing hydrogen by electrolyzing water, the usage amount of the catalyst can be reduced, and meanwhile, the iridium-based catalyst has better mass transfer effect and conductivity, higher catalytic activity and excellent stability.

The invention provides a separation and purification method of urokinase, and relates to the technical field of separation and extraction. The separation and purification method comprises the following steps: S1, regulating the pH value of male urine to 8.5, standing, and taking supernate; s2, mixing the supernate with an adsorption material, and eluting with an eluent to obtain a urokinase crude product solution; the adsorption material is a core-shell silica gel polymer, Fe3O4atSiO2-NH2 is taken as a core, and polystyrene is taken as a shell; the eluent is a sodium citrate buffer solution with the concentration of 0.5 to 0.15 M, acetonitrile with the concentration of 1 to 5 weight percent and EDTA (Ethylene Diamine Tetraacetic Acid) with the concentration of 0.5 to 1.5 mM; and S3, carrying out anion exchange column chromatography on the urokinase crude product solution, eluting with an eluent, and precipitating to obtain the urokinase. The urokinase prepared by the method has the advantages of high polymer urokinase content, high recovery rate and high activity yield.

The invention provides quantum dot aerogel, a quantum dot light-emitting device and a preparation method thereof, and the preparation method comprises the following steps: adding a silane coupling agent into quantum dots to form modified quantum dots with silanol groups on the surfaces; uniformly stirring a silicon dioxide precursor and absolute ethyl alcohol, slowly adding deionized water and a catalyst, and stirring to form silicon dioxide sol; adding the modified quantum dots into silicon dioxide sol to form a mixed solution; placing the mixed solution in a closed container, and standing to form gel; putting the gel into absolute ethyl alcohol for aging treatment; and carrying out supercritical drying treatment on the aged gel to obtain the quantum dot aerogel composite material. The light-emitting performance of the quantum dots and the heat insulation performance of the aerogel are perfectly combined, the high temperature resistance and blue light resistance of the quantum dot aerogel composite material film layer can be greatly improved, the preparation method is simple, and the application range of the quantum dots can be greatly widened.

The present application provides a positive electrode material, and a preparation method therefor and the use thereof. The positive electrode material of the present application comprises a substrate and an island-shaped coating layer provided on the surface of the substrate, wherein the substrate is a lithium-ion layered oxide having an O2 stacking structure; and the coating layer is selected from one or more of the oxides of the element M, the element M being selected from one or more of Al, Mg, Ti, Y, Zr, La, Ce, Pr, Si, Sn, Cu, W, Sm, Gd, In, Zn, and Fe. In the positive electrode material of the present application, by coating the surface of the lithium-ion layered oxide substrate having an O2 stacking structure with the specific island-shaped oxide coating layer, the positive electrode material is made to have relatively high specific capacity, structural stability and positive electrode interface stability at high voltages, thereby obtaining good cycling performance.