1072 results about "Ruthenium" patented technology

The invention relates to the technical field of high-entropy oxide and electrocatalyst synthesis, in particular to a double-phase hollow high-entropy oxide catalyst and a preparation method and application thereof, the double-phase hollow high-entropy oxide catalyst comprises metal elements and non-metal elements, the metal elements comprise ruthenium, nickel, cobalt, iron, manganese and chromium; the non-metallic element is oxygen; the chemical formula of the double-phase hollow high-entropy oxide catalyst is NiCoFeMnCrRuO. The invention further discloses a preparation method of the catalyst. The double-phase hollow high-entropy oxide catalyst has a multi-shell hollow structure, provides a larger specific surface area and exposes a large number of reaction active sites, so that the double-phase hollow high-entropy oxide catalyst has lower overpotential, higher reaction efficiency and good electrochemical stability; meanwhile, the preparation method of the double-phase hollow high-entropy oxide catalyst is simple in process, low in cost, high in repeatability and suitable for industrial mass production, and has a wide application prospect.

Provided herein are methods and apparatuses for reducing line bending when depositing a metal such as tungsten, molybdenum, ruthenium, or cobalt into features on substrates by periodically exposing the feature to nitrogen, oxygen, or ammonia during atomic layer deposition, chemical vapor deposition, or sequential chemical vapor deposition to reduce interactions between metal deposited onto sidewalls of a feature. Methods are suitable for deposition into V-shaped features.

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 rare earth oxide post-supported ruthenium-based ammonia decomposition catalyst, a preparation method and application thereof in hydrogen preparation through ammonia decomposition, and belongs to the technical field of hydrogen production. The ammonia decomposition catalyst takes an oxide or a carbon material as a carrier, firstly, ruthenium metal is loaded to form an active center, then, rare earth oxide is introduced in a post-loading mode, the structure and electronic characteristics of a metal-carrier interface are regulated and controlled, and finally, the ammonia decomposition catalyst with high dispersity and stability is obtained through reduction treatment. The low-temperature ammonia decomposition performance and the operation stability are obviously improved. Under the conditions that the temperature is 400 DEG C and the air speed of ammonia gas is 18000 mL.gcat <-1 >. H <-1 >, the ammonia conversion rate of the catalyst is close to the thermodynamic limit, and the catalyst has good anti-sintering and anti-poisoning capabilities. The catalyst is simple and convenient in preparation process, can be produced on a large scale, is suitable for various scenes of hydrogen production through ammonia decomposition, is particularly suitable for distributed and on-demand hydrogen production systems, and provides powerful technical support for efficient utilization and green conversion of hydrogen energy.

The invention discloses a hydroxyl-rich ruthenium / titanium dioxide catalyst as well as a preparation method and application thereof, and the preparation method comprises the following steps: step 1, loading a ruthenium precursor on a titanium dioxide carrier by adopting an impregnation method or a deposition-precipitation method, and drying and calcining to obtain a Ru / TiO2 catalyst; and step 2, placing the Ru / TiO2 catalyst in an atmosphere environment containing water vapor or forming a physical adsorption water film on the surface of the Ru / TiO2 catalyst, and performing ultraviolet irradiation treatment to obtain the Ru / TiO2 catalyst. According to the method, water is physically adsorbed through ultraviolet light dissociation, hydroxyl is directly generated on the surface of Ru / TiO2 in an in-situ mode, the method is easy to operate, complex liquid phase treatment is not needed, and the stability of the generated hydroxyl under the subsequent high-temperature gas-solid phase hydrogen-rich reaction condition is obviously superior to that of hydroxyl introduced through a traditional method. The stable hydroxyl enriched on the surface serves as an effective Lewis base site and cooperates with a Ru active site, adsorption and activation of CO2 molecules are remarkably promoted, and therefore the catalytic activity of the CO2 methanation reaction is greatly improved.

The invention discloses a catalyst for hydrogen production through tar steam reforming and a preparation method and application thereof. The catalyst comprises a cobalt-magnesium-aluminum composite spinel carrier and an active component loaded on the cobalt-magnesium-aluminum composite spinel carrier, the active component comprises nickel and at least one metal additive selected from iron, zirconium and ruthenium. The preparation method mainly comprises the following steps: preparing the carrier by adopting a coprecipitation method, loading the active component by adopting an impregnation method, and drying and reducing to obtain the final catalyst. The catalyst is used for tar component steam reforming hydrogen production reaction, especially for treating raw materials containing phenol and water vapor at 600-700 DEG C, tar conversion can be efficiently catalyzed, product gas rich in hydrogen can be generated, hydrogen selectivity is high, and almost no methane is generated. The catalyst has the advantages of high activity, good stability, strong carbon deposition resistance and the like, and is suitable for purification and high-value utilization of biomass pyrolysis tar.

The invention relates to the technical field of chemical catalysts, in particular to a cerium-based solid solution loaded iron-based oxygen vacancy enhanced low-temperature ammonia synthesis catalyst. The heterovalent ions are doped in CeO2 crystal lattices to introduce strain and defects, so that the oxygen vacancy formation energy and concentration are greatly improved. Experiments show that the oxygen vacancy concentration (delta) of the Ce0. 8Zr0. 2O2-delta carrier disclosed by the invention can reach 0.12, which is 3-5 times that of pure CeO2. Under the conditions of 250 DEG C and 5 MPa, the ammonia synthesis rate reaches 120 [mu] mol / g / h, which is more than 20 times that of a traditional molten iron catalyst; under the conditions of 350 DEG C and 10 MPa, the ammonia synthesis rate exceeds 1000 [mu] mol / g / h and is close to the level of a noble metal ruthenium-based catalyst. As the working temperature is reduced by 100-150 DEG C, the reaction heat consumption is reduced by more than 30%, and the overall energy consumption is reduced by 25-40%.

This invention relates to a method for using a low-content ruthenium-based catalyst modified with nitrogen and oxygen ligands in the hydrochlorination of acetylene. The invention utilizes 2-pyridine carboxylate as a ligand, commercial activated carbon as a support, trace amounts of ruthenium as the main active component, and water as a solvent. An improved synthesis procedure yields a low-content ruthenium-based catalyst with ruthenium ions coordinated by a modifier and commercial activated carbon as a support, significantly improving catalyst performance while reducing ruthenium content. This catalyst exhibits high activity and vinyl chloride selectivity in the fixed-bed hydrochlorination of acetylene to vinyl chloride, and its low cost makes it highly valuable for industrial applications. The ruthenium loading is 0.1%, and the reaction gas space velocity is 170 h⁻¹. ‑1 V (C2H2) / V (HCl) With a ratio of 1:1.05 and a reaction temperature of 180℃, the acetylene conversion rate can reach 84.3%, the vinyl chloride selectivity is greater than 99%, and the activity remains basically unchanged within 10 hours.

The present invention relates to an ammonia decomposition catalyst and a manufacturing method thereof, and more particularly to an ammonia decomposition catalyst containing alumina (Al2O3), cerium (Ce), lanthanum (La), ruthenium (Ru) and potassium (K).

The invention discloses a method for controlling CMP (chemical mechanical polishing) dish-shaped pits, corrosion pits and interface corrosion of ruthenium barrier layer copper wiring, which is suitable for a manufacturing process of integrated circuits of 14 nanometers and below. According to the method, a specifically synthesized TTAK corrosion inhibitor is introduced into a polishing solution system, the oriented adsorption characteristic of the molecular structure of the TTAK corrosion inhibitor is utilized, the corrosion reaction of copper is selectively inhibited, meanwhile, the normal material removal efficiency of a ruthenium barrier layer and a TEOS dielectric layer is maintained, and cooperative regulation and control of the removal rate of the Cu / Ru / TEOS material are achieved. By means of the method, dished pits, corrosion pits and Fang type interface defects generated in the fine polishing and barrier layer polishing process can be effectively eliminated, and copper / ruthenium interface corrosion is improved. According to the method, the global planarization quality of the copper interconnection ruthenium barrier layer is remarkably improved, the interface bonding strength and the electrical reliability of an interconnection circuit are enhanced, and an effective solution is provided for performance optimization of an advanced process integrated circuit device.

The invention relates to a membrane electrode and application thereof in deuterium-enriched water, and belongs to the field of clean energy development and utilization. The membrane electrode comprises a proton exchange membrane, an anode catalyst and a cathode catalyst, the anode catalyst is an iridium / iridium oxide catalyst with a three-dimensional porous network structure, and the cathode catalyst is a platinum-ruthenium alloy catalyst. The preparation method comprises the following steps: coating one side of the N117 proton exchange membrane with the anode catalyst, coating the other side of the N117 proton exchange membrane with the cathode catalyst, and then performing hot pressing to prepare the membrane electrode. The method comprises the following steps: assembling a membrane electrode into an electrolytic cell, and electrolyzing water by using the electrolytic cell to realize deuterium enrichment. The membrane electrode and the electrolytic cell are reasonable in design, the preparation process is simple and controllable, and the obtained product is high in efficiency and long in service life when used for enriching deuterium and facilitates industrial application.

The invention discloses a surface oxidation monatomic nano-alloy catalyst as well as a preparation method and application thereof, and belongs to the technical field of advanced nano-energy materials and electro-catalysis. A surface-oxidized monatomic nano-alloy catalyst comprises a hydroxylated carbon nanotube carrier and bimetallic nano-alloy particles loaded on the hydroxylated carbon nanotube carrier, in the bimetallic nano-alloy particles, non-noble metal elements are dispersed in noble metal nano-particles in a monatomic form, the size of the bimetallic nano-alloy particles is 3-4 nm, and the surface-oxidized monatomic nano-alloy catalyst is prepared from a surface-oxidized monatomic nano-alloy catalyst. An oxide layer with the thickness of 0.3-0.6 nm is arranged on the surface of the bimetallic nano-alloy particle; the loading amount of the noble metal is 5-15wt%. Ruthenium and other non-noble metal elements are alloyed and anchored on the carbon material substrate, the conductivity of the catalyst can be greatly improved, the size of alloy particles is accurately controlled within the range of 3-4 nm, active sites can be exposed to the maximum extent, and structural stability is considered.

The invention relates to the technical field of catalyst preparation, and discloses a preparation method and application of a ruthenium / cerium oxide composite nanofiber catalyst, and the preparation method comprises the following steps: (1) adding cerium salt and P123 into a mixed solution of DMF (Dimethyl Formamide) and an alcohol solvent according to a molar ratio of 1: (0.1-0.4), stirring and mixing, and carrying out hydrothermal reaction at 160-180 DEG C for 4-12 hours to obtain a spinning solution; (2) performing electrostatic spinning on the spinning solution to obtain a cerium fiber precursor; (3) pre-oxidizing the cerium fiber precursor, and then carrying out aerobic roasting to obtain a cerium oxide nanofiber carrier; and (4) dipping the cerium oxide nanofiber carrier in a ruthenium salt solution, drying, and performing hydrogen reduction to obtain the catalyst. According to the invention, the ruthenium / cerium oxide composite nanofiber catalyst with a unique cavity-containing nanofiber form is prepared by adopting an electrostatic spinning technology, and the ruthenium / cerium oxide composite nanofiber catalyst has good catalytic selectivity and stability in an ammonia decomposition reaction.

The invention belongs to the technical field of catalysts, and discloses an ammonia decomposition hydrogen production catalyst and a preparation method and application thereof. The preparation method of the catalyst for hydrogen production through ammonia decomposition comprises the following steps: in an inert atmosphere, successively carrying out calcination and acid treatment on a carbon carrier to prepare an acid-treated graphitized carbon carrier; adding a ruthenium precursor, a rare earth element precursor and an alkali metal precursor into ethanol, and mixing to prepare a mixed solution; then adding a graphitized carbon carrier into the mixed solution, and mixing; then adding urea and a surfactant, continuously mixing, and standing to obtain a solid precipitate; and finally, carrying out heat treatment on the solid precipitate in a reducing atmosphere. The catalyst takes a highly graphitized carbon material as a carrier, an alkali metal is doped to provide an alkaline environment, and a rare earth metal oxide and Ru form dual-assistant synergistic regulation of an interface, so that low-temperature high-activity ammonia decomposition hydrogen production and long-acting stable operation are realized.

The invention discloses a hydrogen energy fuel cell catalyst carrier based on a graphene graft polymer, which is characterized in that two-dimensional graphene is used as a substrate, the surface of the two-dimensional graphene is modified with an oxygen-containing functional group, and a functional polymer branch chain containing nitrogen, sulfur or phosphorus heteroatoms is covalently grafted to form a local three-dimensional network winding structure; the carrier is loaded with platinum, palladium, ruthenium and other metal or alloy nanoparticles, the particle size is 2-8 nm, the loading capacity is 10%-40%, and the particles are anchored to polymer functional sites or reduced in situ to a graphene defect area through coordination. A polymer branch chain has pH responsiveness and can adjust the local proton transmission efficiency; the grafting density is 3-15 grafting points per 100 carbon atoms, so that high dispersion and stable anchoring of metal particles are effectively realized; the specific surface area of the carrier is 400-800m < 2 > / g, the electrochemical active area is not less than 80m < 2 > / g, and the activity retention rate is greater than 80% after 5000 circles of accelerated durability tests. The activity, the stability and the proton conduction performance of the catalyst are remarkably improved, and the catalyst is suitable for high-performance fuel cells.

The invention relates to the technical field of biological aviation kerosene, and discloses a process for preparing biological aviation kerosene from waste grease. The method comprises the following steps: introducing waste oil into a hydrofining reactor, introducing hydrogen, carrying out a hydrodeoxygenation reaction under the catalysis of a hydrogenation catalyst, carrying out a reaction on the obtained hydrodeoxygenated oil in an isomerization pour point depressing reactor, and finally carrying out isomerization hot high-pressure separation treatment, isomerization cold high-pressure separation treatment and rectification tower segmentation to obtain the biological aviation kerosene. The specific surface area of a carbon matrix of the hydrogenation catalyst is large, the void structure is rich, a large number of Ni-Mo-P active catalytic centers can be exposed, precious metals such as platinum and ruthenium do not need to be added, the hydrodeoxygenation reaction efficiency of waste oil and fat is remarkably improved, the mass fraction of branched paraffin and cycloparaffin in biological aviation fuel is high, and the combustion performance is better.

The invention provides a ruthenium-based carbon dioxide hydrogenation catalyst based on MoS2 as well as a preparation method and application of the ruthenium-based carbon dioxide hydrogenation catalyst. The carbon dioxide hydrogenation catalyst comprises silicon dioxide, ruthenium and molybdenum disulfide, and the ruthenium and the molybdenum disulfide are loaded on the silicon dioxide. Therefore, in the carbon dioxide hydrogenation catalyst, the molybdenum disulfide is used as an auxiliary agent, so that the generation of methane (CH4) can be remarkably inhibited while a high CO2 conversion rate is maintained, the reversion of a product from CH4 leading to carbon monoxide (CO) leading is realized, and the inherent core defects that an existing Ru-based CO2 hydrogenation catalyst is too high in methanation activity, low in CO selectivity and difficult to consider activity-selectivity at the same time are overcome.

The invention relates to the technical field of magnetron sputtering, and provides a preparation method of a ruthenium sputtering target material. The method comprises the following steps: sequentially carrying out hydrogen introduction reduction treatment, crushing and sieving on ruthenium powder to obtain reduced ruthenium powder; and the reduced ruthenium powder is sequentially subjected to compression molding, cold isostatic pressing treatment and sintering treatment, and the ruthenium sputtering target material is obtained. According to the method, the technical problems that the ruthenium sputtering target material is high in oxygen content and random in grain orientation in a traditional powder metallurgy process are effectively solved by combining a dual deoxidization mechanism of'hydrogen feeding reduction-hydrogen sintering 'and cooperative regulation and control of cold isostatic pressing treatment and sintering process parameters. Results of the embodiment show that the ruthenium sputtering target material prepared by the method can realize the following performance indexes: the purity is greater than or equal to 99.95%, the oxygen content is less than or equal to 20 ppm, the average grain size is less than or equal to 2 microns, the density is greater than or equal to 99%, the required specific crystallographic orientation can be stably formed, and a foundation is laid for subsequent magnetron sputtering preparation of a high-performance film.

The invention relates to the field of preparation of nano materials, in particular to a preparation method of a metal-oxide cluster electro-catalytic material based on an ammonia-mediated electrostatic adsorption principle, and aims to solve the problem that a metal-oxide cluster heterogeneous interface is difficult to accurately construct by an existing method. The preparation method comprises the following steps: dispersing a carbon carrier, a soluble inorganic compound containing platinum, ruthenium and rhodium, a soluble metal complex anion salt and dopamine hydrochloride in a water-alcohol mixed solution, adding ammonia water, and preparing a metal-oxide heterogeneous cluster precursor through an ammonia-mediated electrostatic adsorption effect; and pyrolyzing the precursor in a reducing atmosphere to prepare the metal-oxide cluster electro-catalytic material. The prepared electro-catalytic material has a definite heterogeneous cluster interface and has excellent performance in alkaline hydroxide reaction. The method is simple and convenient to operate, low in cost and low in energy consumption, can be popularized to various metal-oxide cluster electro-catalytic materials, and has application potential.

The invention provides a metal Ru catalyst as well as a preparation method and application thereof, and particularly, the metal Ru catalyst is prepared by using a specific carbon source and a ruthenium source as precursors through a simple one-step method. The method is simple in process, low in cost and high in controllability, the obtained metal Ru catalyst has excellent seawater electrolysis activity and stability, the overpotential (mV) shown under 10 mA cm <-2 > under the real seawater condition is 39 mV which is far lower than the overpotential (53 mV) shown under 10 mA cm <-2 > of commercial Pt / C, and the metal Ru catalyst can be applied to the cathodic hydrogen evolution reaction of seawater electrolysis.

The application discloses a kind of heteropoly acid assisted ball milling modified micron zero-valent iron particles, preparation method and application.The micron zero-valent iron particles are mainly prepared by mixing micron zero-valent iron, heteropoly acid and relatively cheap noble metal compound, and the specific preparation is that micron zero-valent iron, heteropoly acid and noble metal compound are placed in a ball mill jar and a specific atmosphere to carry out ball milling modification to obtain heteropoly acid modified ultra-low ruthenium loaded micron zero-valent iron particles.The particles provided by the application have extremely strong reaction performance on chlorinated hydrocarbons, and the performance does not attenuate for more than 30 cycles, and can achieve complete dechlorination on low concentration and high concentration chlorinated hydrocarbons, which has great water treatment application value.

The application discloses a high-activity and high-stability catalyst for synthesizing methacrylonitrile and a preparation method and application thereof, and has the technical scheme that (1) manganese dioxide powder is added into an acid solution and placed in an oven, and the manganese dioxide powder is pickled at 120-150 DEG C for 10-24h; the pickling solution is filtered, washed, dried and calcined to obtain a pickling-treated catalyst carrier; (2) a ruthenium precursor is added into a solvent and fully dissolved to obtain a ruthenium solution; the pickling-treated catalyst carrier is added into the ruthenium solution and loaded under ultrasonic, and then the solution is filtered, washed, dried and calcined to obtain a ruthenium monatomic catalyst. The method is simple, the reaction condition is mild, the production cost is low, raw materials are easy to obtain, the conversion rate of methacrolein is high, the yield of methacrylonitrile is high, and the stability is good.

The invention belongs to the technical field of hydrogen production catalysis, and particularly relates to an ammonia decomposition hydrogen production catalyst and a preparation method thereof. According to the catalyst for hydrogen production through ammonia decomposition, potassium-modified porous aluminum oxide serves as a carrier of the catalyst, ruthenium serves as an active component of the catalyst, and ruthenium is mainly loaded on the surface of the carrier and is of a core-shell structure. The prepared catalyst for hydrogen production through ammonia decomposition has high activity, high stability and high mass transfer performance, the preparation technology is simple, the whole process is environmentally friendly and green, and the catalyst is suitable for large-scale production.

The invention is suitable for the technical field of water electrolysis hydrogen production, and provides an alkyne-rich carbon-ruthenium nickel alloy catalyst and a preparation method and application thereof. The preparation method comprises the following steps: simultaneously adding a ruthenium salt solution, a nickel salt solution and an organic molecule solution into an alkyne-enriched carbon dispersion liquid for reaction; and carrying out centrifugation, cleaning and vacuum drying treatment on the reacted mixed solution to obtain the alkyne-rich carbon-ruthenium nickel alloy catalyst. According to the invention, the acetylene-rich carbon-ruthenium nickel alloy catalyst uniformly loaded with ruthenium nickel (RuNi) clusters is successfully prepared. In the performance evaluation of hydrogen production by water electrolysis in a simulated seawater environment, the material shows excellent hydrogen evolution activity as a cathode catalyst. Experimental results show that under the applied potential of-0.6 V (relative to a reversible hydrogen electrode, RHE), the absolute value of the current density can reach 0.847 A cm <-2 > to 0.896 A cm <-2 >. The invention provides a feasible material solution for developing a high-performance water electrolysis hydrogen production catalyst suitable for a complex water quality environment.

The invention belongs to the technical field of anion exchange membrane fuel cells, and discloses a high-stability ruthenium-based hydroxide electrocatalyst used as an anode of an anion exchange membrane fuel cell and a preparation method of the high-stability ruthenium-based hydroxide electrocatalyst. The catalyst is prepared by taking ruthenium as a unique active component, fullerene (C60) as a carbon substrate and polydopamine (PDA) as an additive through argon heat treatment. The preparation method disclosed by the invention is simple and easy to implement, and through the design scheme that C60 with high electron affinity is used as a carrier, the electronic structure of a ruthenium active site is effectively adjusted, and excessive adsorption of a ruthenium-based catalyst to hydroxyl species in a hydrogen oxidation reaction (HOR) process is weakened, so that the ruthenium reaction active site is greatly reserved for hydrogen adsorption, and the hydrogen adsorption efficiency is improved. Therefore, the stability of ruthenium-based electro-catalysis in hydrogen oxidation reaction can be greatly improved.

The invention discloses a catalyst for preparing cyclohexanone by cyclohexanol dehydrogenation coupled phenol hydrogenation, the catalyst has a composite metal hydrotalcite structure, the metal components comprise ruthenium, magnesium and aluminum, the metal components are uniformly dispersed in hydrotalcite, and the ruthenium, the magnesium and the aluminum respectively account for 1-5wt%, 10-30wt% and 1-10wt% of the total mass of the catalyst. The acid-base property, the specific surface area and the pore structure of the catalyst are optimized by adjusting the ratio of magnesium to aluminum, so that the dispersion of ruthenium is improved, the interaction between ruthenium and a hydrotalcite carrier is increased, and the synergistic effect of all the element components enables active centers in cyclohexanol dehydrogenation, hydrogen transfer and phenol hydrogenation processes to be efficiently combined together, so that the catalytic activity of the catalyst is improved. Rich alkaline sites are generated in the catalyst, the dehydration side reaction of cyclohexanol can be effectively inhibited, meanwhile, the selectivity of cyclohexanone prepared through phenol hydrogenation is improved, it is ensured that the phenol hydrogenation reaction and the cyclohexanol dehydrogenation reaction can be effectively coupled, and cyclohexanone is efficiently prepared.

The invention provides a gradient composite graphene electrolysis electrode plate and an in-situ preparation method thereof. The electrode plate comprises a metal conductive base material (such as titanium alloy), a porous ceramic skeleton layer (Al2O3-40% ZrO2, the porosity of which is 30 + / -5%), a chemical copper plating layer for filling pores, an electroplated nickel-ruthenium alloy catalytic layer (Ni: Ru = 9: 1) and 3-5 graphene functional layers (ID / IG is less than or equal to 0.08) grown in situ, wherein the porous ceramic skeleton layer (Al2O3-40% ZrO2) is laser-cladded on the surface of the porous ceramic skeleton layer (Al2O3-40% ZrO2). The preparation method comprises the following steps: performing laser cladding on a ceramic skeleton, wherein the power density is 300-500W / mm < 2 >, and sintering at 1600 DEG C to form metallurgical bonding; gradient plating: electroless copper plating (containing nano-diamond enhancement) and pulse electroplating of Ni Ru (duty ratio is 1: 5); and performing directional CVD growth: after reducing the catalyst layer by H2 at 1050 DEG C, introducing CH4 / H2 (the volume ratio is 1: 4) in a pulse manner, and realizing full coverage of the inner wall of the mesh by vortex air intake. The technical effects are as follows: (1) the overpotential of chlorine evolution in saturated salt water at 80 DEG C is as low as 268mV (1A / cm < 2 >); (2) strong acid environment service life gt; the time is 100 thousand hours (12 times that of the national standard); (3) the production cost is lt; and 620 / m < 2 > (90% lower than that of a traditional ruthenium-iridium coating). The problems of graphene transfer damage and special-shaped electrode covering are solved.

The invention belongs to the technical field of heterogeneous phase intermetallic compounds, and discloses a ruthenium-germanium heterogeneous phase intermetallic compound and a preparation method and application thereof. The preparation method comprises the following steps: step 1, dissolving Ge precursor salt, Ru precursor salt and a carrier material in a water-soluble polymer solution; the mmol ratio of the Ru precursor salt to the Ge precursor salt is 0.05: (0.05-0.09); step 2, performing freeze drying treatment on a product in the step 1; 3, performing high-temperature heat treatment on the product obtained in the step 2 in a reducing atmosphere at the temperature of 800-1000 DEG C, and preparing the ruthenium-germanium heterogeneous phase intermetallic compound after the high-temperature heat treatment; according to the ruthenium-germanium heterogeneous phase intermetallic compound prepared through the preparation method, the ruthenium-germanium heterogeneous phase can be obviously observed through a spherical aberration electron microscope, the synergistic effect is generated through strong interaction among different components, the physical and chemical properties of the material can be obviously optimized, and when the ruthenium-germanium heterogeneous phase intermetallic compound is used as a catalyst, the catalytic effect is extremely good.

The present invention addresses the problem of providing: a technology related to a catalyst for a Fischer-Tropsch synthesis reaction (FT synthesis reaction) capable of, in the FT synthesis reaction, more easily obtaining a hydrocarbon having a specific number of carbon atoms, and a method for producing said catalyst; and a technology related to a hydrocarbon production apparatus and a hydrocarbon production method.　In order to solve said problem, provided are: a catalyst for FT synthesis, in which an active metal is supported on the surface of a carrier, the carrier contains silicon or aluminum, the active metal contains at least one selected from cobalt, ruthenium, and iron, and the metal density per specific surface area of the carrier is within a specific range; a method for producing said catalyst; and a hydrocarbon production apparatus and a hydrocarbon production method using the catalyst.　According to the present invention, it is possible to: improve the CO conversion rate in an FT synthesis reaction and improve the selectivity of the number of carbon atoms in an obtained hydrocarbon; and more easily generate a hydrocarbon having a specific number of carbon atoms.

The invention relates to the field of efficient integrated assemblies of PEM water electrolysis hydrogen production systems, and discloses an efficient integrated assembly for a PEM exchange membrane water electrolysis hydrogen production system, an anode electrode unit in the integrated assembly comprises a ruthenium-based high-entropy metal oxide electrocatalyst, and the ruthenium-based high-entropy metal oxide electrocatalyst comprises ruthenium, tin, manganese, chromium and tantalum elements; the preparation method of the ruthenium-based high-entropy metal oxide electrocatalyst comprises the following steps: grinding solid inorganic ruthenium salt, tin salt, manganese salt, chromium salt, tantalum salt and sodium chloride to obtain a metal salt mixture; carrying out ball milling to obtain a high-entropy metal oxide precursor; and carrying out heat treatment and water washing treatment on the precursor to obtain the ruthenium-based high-entropy metal oxide electrocatalyst. The invention also discloses application of the electrocatalyst in water electrolysis oxygen evolution reaction in an acid solution and water electrolysis hydrogen production reaction of a PEM proton exchange membrane, and the electrocatalyst shows excellent electrocatalytic activity.