2588 results about "Hydrogen evolution" patented technology

The invention discloses a pipe network health real-time monitoring system and an evaluation method. According to the invention, through real-time health monitoring and dynamic deduction capability, the flexibility and safety of energy supply are significantly improved. The healthy twin module constructs a digital mirror image of the full life cycle of energy equipment, solar hydrogen production efficiency fluctuation, hydrogen storage tank pressure change and fuel cell attenuation trend can be accurately tracked, and risk points such as electrolytic cell abnormal hydrogen evolution and proton exchange membrane aging can be recognized in advance. The all-weather transparent monitoring enables the system to dynamically adjust the ratio of hydrogen production to power generation, the fuel cell is automatically switched to supply power in cloudy and rainy days, continuous energy supply is guaranteed, and the system can generate a coping plan in advance by simulating extreme scenes such as sudden drop of photovoltaic output and hydrogen leakage, so that the system is convenient to use. The energy interruption risk caused by sudden equipment failure is greatly reduced, meanwhile, the service life of key components is prolonged, the maintenance cost of a distributed energy network is reduced, and meanwhile the overall energy efficiency utilization rate is also improved.

The invention discloses an alkaline electrolytic water hydrogen evolution electrode, a preparation method thereof and an electrolytic bath based on the electrode. The electrode comprises a nickel net base material, raney nickel located on the nickel net base material and a catalytic layer which is electrochemically deposited on the surface of the raney nickel to cover a zigzag edge to form a smooth surface. The catalytic layer is a platinum catalytic layer, a nickel-sulfur alloy catalytic layer, a nickel-cobalt-zinc layer or a nickel-iron-zinc layer, and an electroplate liquid for electrochemical deposition comprises sulfosalicylic acid. According to the electrolytic cell, an alkaline electrolytic water hydrogen evolution electrode is used as a cathode, and Raney nickel / nickel net is used as an anode. According to the alkaline electrolytic water hydrogen evolution electrode, the catalyst layer which is high in binding force with the base material is deposited on the Raney nickel / nickel net base material in a specific electrochemical deposition mode, and the catalyst layer can effectively cover the sawtooth-shaped edge of the surface of the electrode and keep a part of the original high-specific-surface-surface structure of Raney nickel at the same time; the catalytic performance of the electrode is improved, and the overpotential of the electrode under 100mA / cm < 2 > can be lower than 241mV.

The invention discloses a complex electrolyte additive for a battery, an aqueous zinc ion battery electrolyte and an aqueous zinc ion battery. The electrolyte additive is a complex containing metal complex ions; the complex is composed of a central ion and an internal ligand. The electrolyte additive can respectively form metal and alloy electrode-electrolyte interfaces on the surface of a zinc negative electrode through replacement and electrochemical reaction, and regulate and control the deposition behavior of zinc ions to inhibit the generation of zinc dendrites and accelerate deposition / dissolution kinetics, so that the service life of the zinc negative electrode is remarkably prolonged, and the rate capability is enhanced; a solvation structure of zinc ions can be regulated and controlled, side reactions such as hydrogen evolution, corrosion and passivation are slowed down, and capacity fading of the water-based zinc ion battery can be remarkably delayed when the positive electrode is coupled with a high-efficiency positive electrode; meanwhile, the aqueous zinc ion battery electrolyte additive is low in price, green, environment-friendly, high in functionality and beneficial to development of an aqueous zinc ion battery electrolyte and an aqueous zinc ion battery which are excellent in performance, safe, environment-friendly and low in cost.

The invention discloses a preparation process of a modified porous carbon material catalyst. The preparation process comprises the following steps: (1) mixing and calcining a biomass precursor and a template agent to prepare graded porous carbon; (2) low-frequency plasma pretreatment and high-frequency plasma fluorination modification are adopted; (3) introducing the pulse plasma into a nitrogen doping site; (4) spraying ionic liquid and activating H2 plasma to form a B / F co-doped layer; and (5) loading alloy nanoparticles such as PtRu through pulse electrodeposition. According to the obtained catalyst, biomass derived porous carbon serves as a carrier, a fluorine / nitrogen co-doped active layer is constructed on the surface of the carrier through multi-frequency plasma synergistic modification and ionic liquid auxiliary modification, superfine precious metal nanoparticles are loaded, the hydrogen evolution overpotential of the catalyst is smaller than or equal to 28 mV under the current density of 10 mA / cm < 2 >, the activity attenuation is smaller than 5% after 1000 times of circulation, and the catalyst has a good catalytic activity. The water electrolysis hydrogen production device is suitable for a large-scale water electrolysis hydrogen production device.

Nanomaterials and methods of preparation and use thereof, are disclosed. The nanomaterials include a non-noble metal substrate and noble metal atoms on a surface of the non-noble metal substrate. The noble metal atoms simultaneously coordinate with a halogen and oxygen. The substrate has a large specific surface area and a large electrochemical active area, and the surface coordination environment of the noble metal affects the electronic structure and catalytic activity of a resulting catalyst. The noble metal surface coordination structure may be regulated and controlled by a synthesis temperature, an alkalinity, a reaction time, and an electrodeposition voltage range. A hydroxide ion and the halogen coordinate with the noble metal, exhibiting an unsaturated pentacoordinate state. Doping the substrate with reducing metal ions may increase the loading capacity, anchor the noble metal atoms, and improve anodic oxygen evolution and cathodic hydrogen evolution in seawater electrolysis.

The present application relates to the technical field of catalysts and relates to a non-noble metal cathode hydrogen evolution catalyst for PEM water electrolysis and a use thereof. The present application provides a method for preparing a cathode hydrogen evolution catalyst. A nickel-molybdenum heteropoly acid having a specific structure is generated in situ on the surface of a porous carbon material carrier, and is used as a hydrogen evolution catalyst active component precursor, and an in-situ generated nickel-containing molybdenum sulfide active component is subjected to sulfidation treatment to prepare a non-noble-metal-supported cathode hydrogen evolution catalyst, wherein the in-situ generated nickel-containing molybdenum sulfide active component has a hydrogen adsorption free energy similar to that of Pt and catalytic hydrogen evolution activity, the dispersity is good, and the number of active sites is large, thereby reducing the costs of the catalyst; in addition, during the sulfidation treatment of the nickel-molybdenum heteropoly acid, nitrogen or phosphorus atoms in the carrier can be doped into the lattice of molybdenum disulfide, thereby reducing the hydrogen evolution Gibbs free energy of sulfur atoms on an MoS2 crystal basal surface, and more active sites are formed on a sulfur edge and a molybdenum edge, facilitating a hydrogen evolution reaction.

The invention provides a hydrogen production electrode doped with platinum, ruthenium, tin and praseodymium, a preparation method of the hydrogen production electrode and a water electrolysis hydrogen production device, and relates to the field of water electrolysis hydrogen production. The preparation method of the hydrogen production electrode doped with platinum, ruthenium, tin and praseodymium comprises the following steps: coating the surface of a conductive substrate with mixed powder; the conductive base material coated with the mixed powder is subjected to thermal oxidation treatment, the mixed powder comprises first metal powder, second metal powder and a pore forming agent, the first metal powder comprises Ni powder, and the second metal powder comprises Pt powder, Ru powder, Sn powder and Pr powder; and putting the structure subjected to thermal oxidation treatment into an alkaline solution, and activating to obtain the hydrogen production electrode doped with platinum, ruthenium, tin and praseodymium. The platinum, the ruthenium, the tin and the praseodymium are introduced into the hydrogen production electrode, so that the hydrogen evolution overpotential can be reduced. The hydrogen production electrode prepared by the method disclosed by the invention has relatively high catalytic activity, relatively high stability and a uniformly distributed porous structure, the electrolytic efficiency can be remarkably improved, and the service life of equipment is prolonged.

The invention relates to the technical field of electrochemical carbon dioxide reduction reaction catalysts, and discloses a preparation method and application of a mixed ionomer modified cuprous oxide catalyst, a hydrophobic ionomer and a proton exchange ionomer are used for performing surface modification on cuprous oxide powder, an effective hydrophobic structure is constructed on a Cu2O active site in a physical coating form, and the cuprous oxide modified cuprous oxide catalyst is prepared. A stable and controllable hydrophobic gas-liquid-solid three-phase reaction micro-interface is formed, so that the problems of low C-2 Faraday efficiency, poor selectivity, serious competitive hydrogen evolution reaction, carbonate deposition and the like in the existing process of preparing a C-2 product by electrocatalytic carbon dioxide reduction are solved, and the industrial current density (gt; and the method has the advantages of simple process flow, low price, high product selectivity and the like.

The invention belongs to the technical field of electro-catalysis and energy conversion, and provides a carbon skeleton loaded platinum monatomic-cobalt nanoparticle catalyst, a preparation method thereof and application in electro-catalysis hydrogen evolution, a ZIF-67-ZIF-8 precursor is prepared in an epitaxial growth mode, and the precursor is pyrolyzed to construct a carbon matrix containing cobalt nanoparticles; in the preparation process of ZIF-67-ZIF-8, the treatment duration of tannic acid is regulated and controlled, and the size of cobalt nanoparticles is accurately controlled; meanwhile, uniform N holes generated in the high-temperature pyrolysis process are beneficial to precise range limitation of PtN bonds, and finally the carbon skeleton loaded platinum monatomic-cobalt nanoparticle catalyst is constructed. The concentration of local protons around platinum sites is enriched through cobalt, and therefore adsorption of protons on platinum single atoms and generation of hydrogen are remarkably promoted. Due to the display of the bifunctional catalytic effect, the overall catalytic efficiency of the alkaline hydrogen evolution reaction is effectively improved. The catalyst shows excellent catalytic performance in alkaline hydrogen evolution reaction, and is expected to be widely applied to the water electrolysis hydrogen production technology.

The invention provides a platinum-carbon catalyst taking hollow carbon nanospheres as a carrier and a preparation method of the platinum-carbon catalyst. The method comprises the following steps: adding a polymer monomer into a nano template dispersion liquid with a uniform size; then adding a proper amount of platinum salt into the solution to obtain a mixed solution, and stirring to react for 0.5-30 hours to obtain a reaction product; and annealing the reaction product, and then removing the nano template to obtain the platinum-carbon catalyst. The obtained platinum-carbon catalyst takes the hollow carbon nanospheres as a carrier and has a larger specific surface area, the platinum catalyst is loaded on the surfaces of the carbon nanospheres and can be in better contact with an electrolyte, and the obtained catalyst has good electrochemical activity and shows excellent electro-catalytic hydrogen evolution performance and oxygen reduction performance; and the related preparation method is simple and reliable, is suitable for preparation of an electrocatalytic hydrogen evolution electrode and an oxygen reduction electrode, and has a good application prospect in the fields of proton exchange membrane electrolytic cells, hydrogen fuel cells and the like.

The invention belongs to the technical field of water electrolysis hydrogen production, and particularly relates to an electrolytic hydrogen production electrolytic bath. Comprising a composite electrode assembly; the composite electrode assembly comprises an electrode frame, a bipolar plate, an electrode conductive frame, an oxygen evolution electrode and a hydrogen evolution electrode, the electrode frame is arranged on the outer side of the bipolar plate, the electrode frame and the bipolar plate are both made of plastic materials, the electrode conductive frame is arranged in the electrode frame, and the oxygen evolution electrode and the hydrogen evolution electrode are arranged on the two sides of the bipolar plate respectively and both connected with the electrode conductive frame. By adopting the plastic-based bipolar plate, a sealing effect can be achieved, a sealing gasket part of a traditional electrolytic cell is removed, and the cost of the electrolytic cell is greatly reduced; and the plastic-based bipolar plate, the electrode and the electrode conductive frame are integrated into a whole, so that the assembling and integrating process of the electrolytic cell is greatly simplified.

The invention belongs to the technical field of zinc battery electrolyte, and discloses application of pyridine hydrochloride as an electrolyte additive in stabilizing a zinc negative electrode and realizing four-electron transfer of a zinc-iodine secondary battery. The hydrochloride containing the pyridine structure is used as an electrolyte additive, molecules of the pyridine structure are adsorbed on the surface of the zinc negative electrode to form a shielding layer, the deposition / stripping reversibility of the zinc negative electrode is improved, stabilization of the zinc negative electrode can be achieved, and the problems of zinc dendritic crystal, corrosion and hydrogen evolution are solved. Meanwhile, molecules with pyridine structures can activate and stabilize I- / I0 / I < + > four-electron redox reaction, inhibit I < + > hydrolysis side reaction and improve the energy density and cycling stability of the zinc-iodine battery. The problem of poor electrochemical deposition / stripping reversibility of a zinc negative electrode and the problem of poor stability of positive valence I < + > species of an iodine positive electrode of a four-electron transfer reaction are solved. The electrolyte containing the additive is low in cost, simple in method, easy to produce and high in practical value.

The invention belongs to the field of electrochemistry, and particularly relates to a method for electrochemical lithium extraction of a decommissioned lithium battery assisted by a pseudocapacitor cathode, which comprises the following steps: a) providing an anode electrode and a cathode electrode; the anode electrode is an anode electrode made of a recycled retired lithium battery anode material or an retired lithium battery anode plate; the cathode electrode contains a Prussian blue analogue, the Prussian blue analogue is prepared by mixing citrate, transition metal salt and cyanide in water for reaction, and the transition metal salt is one or more of cobalt salt, ferric salt, copper salt and nickel salt; and b) immersing the anode electrode and the cathode electrode into the electrolyte, and electrifying to carry out electrochemical lithium extraction. According to the method, a pseudocapacitance material with a lithium discharging characteristic is adopted as a cathode to replace a common metal pole plate or a carbon material, a pseudocapacitance reaction with a corrected electrode potential is adopted to replace a hydrogen evolution reaction on the cathode of an existing system, and finally, low-energy-consumption and high-selectivity recovery of lithium is realized.

The invention discloses an efficient difunctional alkaline electrolysis water electrode which comprises a nickel net, an N deposition layer is deposited on the surface of the nickel net, and a NiFeW alloy layer is deposited on the surface of the N deposition layer. The invention further discloses a preparation method of the electrolyzed water electrode. The preparation method comprises the following steps: pre-treating the nickel net substrate; dissolving a nickel salt, a conductive salt and an additive in water to obtain a nickel electrodeposition solution; dissolving a nickel salt, an iron salt, a tungsten salt and an additive in water to obtain a nickel-iron-tungsten electro-deposition solution; and then the nickel net substrate is placed in a nickel electrodeposition solution to be subjected to constant-current deposition, a first electrode of an N deposition layer loaded on the nickel net substrate is obtained, the first electrode is placed in a nickel-iron-tungsten electrodeposition solution to be subjected to constant-current deposition, an N < iFeW > alloy layer loaded on the N deposition layer is obtained, and a finished electrode is obtained. The method has the advantages of low hydrogen evolution overpotential, low oxygen evolution overpotential, good stability, short-time deposition at room temperature, simplicity, easiness in control and low cost, and can be expanded to actual industrial application.

The invention relates to a NiCoW-CoP / Co3O4 (at) NF self-supporting heterostructure catalyst and a preparation method thereof. The preparation method comprises the following steps: preparing a CoP-coated NF precursor on foamed nickel through a constant potential electrodeposition method, then carrying out annealing treatment in a muffle furnace, and finally carrying out electrodeposition on NiCoW-LDH to obtain the NiCoW-CoP / Co3O4-coated NF material. According to the preparation method, the microsphere material with the surface covered with the dendritic dendrites is synthesized, and exposure of active sites is increased through the special surface structure of the microsphere material. The compounding of the trimetal hydroxide containing high-valence tungsten and the introduction of oxygen vacancies can effectively enhance the local electron density of oxygen atoms on the surface of the catalyst, thereby enhancing the catalytic performance and seawater corrosion resistance of the material. Compared with the prior art, the method disclosed by the invention is simple to operate and low in cost, and the prepared catalyst has high electrocatalytic activity, relatively low hydrogen evolution overpotential and oxygen evolution overpotential and long-time stability. And the method has important theoretical significance and potential application value for developing a bifunctional electrocatalyst suitable for electrolyzing seawater.

The invention discloses a zinc-bromine flow battery multifunctional negative electrode electrolyte and a preparation method thereof, and belongs to the technical field of electrochemical energy storage, and the method comprises the following steps: uniformly stirring and mixing a solvent, deionized water and a cosolvent, adding an electrolyte, stirring until the electrolyte is completely dissolved, then adding a supporting electrolyte and a negative electrode additive, stirring until the supporting electrolyte and the negative electrode additive are completely dissolved, and obtaining the zinc-bromine flow battery multifunctional negative electrode electrolyte. The multifunctional negative electrode electrolyte of the zinc-bromine flow battery is obtained; the negative electrode cosolvent is dimethylformamide; and the negative electrode additive is at least one of saponin and cinnamyl aldehyde. Saponin molecules are adsorbed on the surface of the zinc electrode, and electronegative carboxyl groups of the saponin molecules form an electrostatic repulsion net in an electric double layer, so that zinc ions are forced to be uniformly dispersed, local ion concentration hot spots are eliminated, and dendritic crystal nucleation is inhibited from the source. In cinnamyl aldehyde, the strong electronegativity of oxygen atoms and the electronegativity of aldehyde oxygen are far higher than those of hydrogen, so that electrons are strongly attracted, adjacent carbon atoms are positively charged, polar adsorption sites are formed, the hydrogen evolution reaction is effectively inhibited, and the stability and the cycle life of the battery are greatly improved.

Improved electrocatalysts for promoting a hydrogen evolution reaction (HER) or an oxygen evolution reaction (OER) from alkaline fresh water and seawater are disclosed. By incorporating metals, such as tungsten and rare earth elements, into the nickel molybdenum nitride framework, Ni1-xMoxN, the disclosed electrocatalysts demonstrate improved catalytic activity and stability compared to the original Ni&Ni0.2Mo0.8N catalysts, particularly under high-current alkaline conditions, in water electrolysis for hydrogen and oxygen production.

The invention belongs to the technical field of electrocatalytic materials, and relates to a two-phase bimetallic carbide heterostructure electrocatalyst and a preparation method and application thereof. The composition of the two-phase bimetallic carbide heterostructure electrocatalyst is WMoC2 / WVC2, and preferably, the mass percent of the WMoC2 is 40%-80%, and the mass percent of the WVC2 is 20%-60%. According to the invention, the bimetallic heterostructure WMoC2 / WVC2 electro-catalytic hydrogen evolution material is prepared through a step-by-step hydrothermal method and a solid-phase reaction method. The preparation method is green and pollution-free, the raw material cost is low, and the electrocatalytic activity in an alkaline environment is good.

The invention belongs to the field of secondary batteries, and particularly relates to an aqueous zinc ion battery electrolyte additive and an electrolyte. The additive is a beta-diketone organic reagent. When the additive is added into the zinc salt-containing electrolyte, dendritic crystal growth and hydrogen evolution corrosion of zinc can be remarkably inhibited, so that the cycle performance and coulombic efficiency of the zinc ion battery are improved. According to the invention, the zinc ion battery has good cycle performance, is easy for industrial production, and has an application prospect in the technical field of energy storage.

The invention relates to the technical field of oil and gas field produced water, and discloses a method for degrading organic matters in oil and gas field produced water through electrochemical lithium extraction coupled with electrooxidation. The method comprises the following steps: (1) preparing a hydrophilic-oleophobic lithium ion sieve electrode; (2) electrochemical lithium extraction is coupled with electrooxidative degradation of organic matters, wherein a first electrochemical reaction system is constructed, and the first electrochemical reaction system comprises an anode, a cathode, a sealed electrolytic tank, a wire and a voltage-stabilized direct-current power supply; and (3) electrochemical enrichment lithium coupling hydrogen evolution: constructing a second electrochemical reaction system, wherein the second electrochemical reaction system comprises an anode, a cathode, a sealed electrolytic tank, a wire and a voltage-stabilized direct-current power supply. According to the method for degrading the organic matters by coupling electrochemical lithium extraction and electrooxidation of the oil and gas field produced water, circulation of lithium extraction and release and synchronous degradation of organic pollutants can be realized.

The present invention discloses a Ni‑Se‑C hydrogen evolution electrode and a preparation method thereof, belonging to the technical field of electrocatalytic hydrogen evolution. The Ni‑Se‑C hydrogen evolution electrode is composed of a conductive substrate and a Ni‑Se‑C coating electroplated on the surface of the conductive substrate. First, the conductive substrate is pretreated in the present invention; then, Ni, Se, and C elements are deposited on the pretreated conductive substrate by electroplating to form a Ni‑Se‑C hydrogen evolution electrode with excellent hydrogen evolution performance. The synthesis method of the present invention is simple and the catalytic layer structure is stable. The synthesized Ni‑Se‑C hydrogen evolution electrode can be widely applied to the industrial production of hydrogen by electrolyzing water, and has significant practical value and economic value.

The invention relates to a ruthenium nano-cluster / trinickel disulfide heterojunction composite material as well as a preparation method and application thereof. According to the composite material, foamed nickel serves as a substrate material, a Ni3S2 nanosheet array grows on the surface of the substrate material in situ, and ruthenium nanoclusters are anchored on the surface of the Ni3S2 nanosheet array to form the heterojunction composite material. According to the preparation method, the Ni3S2 nanosheet array grows on the foamed nickel substrate in situ, then the composite material with the ruthenium nanocluster anchored on the Ni3S2 surface is prepared through a chemical etching method, and the preparation method is simple, relatively low in cost and suitable for large-scale production; the prepared heterojunction composite material forms a nanosheet array structure and shows a honeycomb structure, so that the catalyst has a relatively large specific surface area, provides more active sites for catalytic reaction, is high in catalytic activity, and can be used as a catalyst applied to hydrogen evolution and oxygen evolution of water electrolysis reaction in electro-catalysis.

The present invention discloses an aqueous zinc-ion battery, comprising: a positive electrode sheet, a negative electrode sheet and an electrolyte. The positive electrode material of the positive electrode sheet is a layered vanadium-based positive electrode material. Since cations and water molecules are inserted into the layers of vanadium pentoxide, the interlayer spacing is increased and the structure of the host material is supported and stabilized. Therefore, the fast and reversible insertion and extraction performance of charge and discharge ions can be improved, and the high rate and long cycle life of the layered vanadium-based positive electrode material can be achieved. The negative electrode sheet is a zinc foil with a surface coating. By defining the thickness of the surface coating to be 100 nm to 20 μm, the surface coating can prevent the zinc foil from directly contacting the electrolyte, and zinc will be deposited between the coating and the zinc foil during the charge and discharge process. In this way, the direct contact between zinc and the electrolyte is avoided, which helps to solve problems such as dendrites, corrosion and hydrogen evolution of the zinc negative electrode. Compared with the traditional aqueous zinc-ion battery, the electrochemical performance of this aqueous zinc-ion battery is enhanced.

The invention discloses a synthesis method of an in-situ carbon-loaded osmium-platinum single-phase solid solution nano-alloy catalyst and application of the nano-alloy catalyst in a hydrogen evolution reaction, and solves the technical problems that when an existing osmium-platinum alloy catalyst is used, the loading process is tedious and time-consuming, and the catalytic performance becomes poor due to non-uniform loading. The method comprises the following steps: respectively weighing an osmium compound and a platinum compound, mixing the osmium compound and the platinum compound, and adding the mixture into a polyol solvent until the mixture is completely dissolved to obtain a precursor solution; the preparation method comprises the following steps: preparing a carbon carrier, adding the carbon carrier into a polyol solvent until the carbon carrier is completely dissolved to obtain a carrier solution, and heating the carrier solution to 150-300 DEG C; in an inert atmosphere, adding the precursor solution into the heated carrier solution within two minutes, uniformly stirring, and preserving heat to obtain a mixed solution; and sequentially washing, centrifuging and drying to obtain the in-situ carbon loaded osmium-platinum solid solution nano-alloy catalyst. The method is simple in synthesis and high in synthesis efficiency, and the catalyst which is uniformly dispersed in a loaded state can be obtained.

The invention belongs to the technical field of electro-catalysis full water splitting, and discloses a nickel-based self-supporting hydrogen evolution electrode and a preparation method and application thereof.The preparation method comprises the steps that nickel chloride hexahydrate and terephthalic acid are dissolved in N, N-dimethylformamide, the concentration of the nickel chloride hexahydrate is controlled to be 0.1-0.15 mol / L, the concentration of the terephthalic acid is controlled to be 0.1-0.15 mol / L, the nickel chloride hexahydrate and the terephthalic acid are stirred to be uniform, ultrasonic treatment is conducted, and an electrolyte is obtained; the pretreated foamed nickel is immersed in the electrolyte to serve as a working electrode, a platinum net serves as a counter electrode, an Ag / AgCl electrode is adopted as a reference electrode, current of-10 mA to-20 mA is applied for deposition for 1.5-2.5 h, and the nickel-based self-supporting hydrogen evolution electrode is obtained after electro-deposition and cleaning and drying are conducted. The nickel-based self-supporting catalytic material prepared by the invention fully exposes active sites, has high catalytic performance, has a good application prospect in the technical field of electro-catalytic materials, and is expected to improve energy and environment problems.

The invention discloses a method for constructing a foamed nickel hydrogen evolution electrode with a multi-layer gradient structure based on two-step electrodeposition. According to the method, the in-situ growth of a multilayer gradient structure catalyst layer is realized by regulating and controlling the current density, and the core process comprises the following steps: 1, pretreatment of an electrode substrate: carrying out ultrasonic cleaning on foamed nickel through hydrochloric acid, absolute ethyl alcohol and deionized water in sequence, and removing surface impurities; 2, step-by-step electro-deposition of the gradient catalyst layer: firstly, electro-deposition is carried out under low current density to form a uniform and compact transition catalyst layer, the contact area between the catalyst layer and the base material is increased, and the durability and stability of the catalyst layer are improved; and then switching to high current density for bubble template method electrodeposition, spontaneously forming a catalyst layer with an inverted cone-shaped hole array structure by utilizing the dynamic template effect of violent hydrogen evolution bubbles, and promoting rapid removal of the bubbles by utilizing the hole array. The electrode prepared by the method has excellent stability, bubble removal capability and catalytic activity in hydrogen evolution reaction.

The present invention relates to the field of water electrolysis and hydrogen production. Disclosed is a carbon nanotube-supported nitrogen-doped catalyst. The catalyst has a carbon nanotube structure as a support, and cobalt and ruthenium as active components, wherein the content of the cobalt element is 30-45w%, the content of the ruthenium element is 1-7wt%, and the proportion of the ruthenium element present in the form of RuN is 60-90wt% relative to the total ruthenium element. A graphitized structure of the catalyst is conducive to charge conduction, Ru is uniformly loaded on the surface of the support by means of a low-temperature reduction process and interaction with defect sites on the surface of the support, and then after high-temperature roasting, Ru interacts with the N element and the metal Co, thereby improving the hydrogen evolution catalytic activity of the catalyst.

The invention relates to a MnWO4 / ZnIn2S4 heterojunction photocatalyst as well as a preparation method and application thereof, and belongs to the technical field of photocatalytic materials. In the experiment process, MnWO4 is dissolved in a precursor solution of ZnIn2S4, the MnWO4 / ZnIn2S4 heterojunction composite materials with different molar ratios are obtained by changing the molar ratio of an Mn source, and the MnWO4 / ZnIn2S4 heterojunction composite materials can be applied to the field of hydrogen evolution through photocatalytic water decomposition. Compared with an existing photocatalyst, the MnWO4 / ZnIn2S4 heterojunction has the advantages that the controllability is good when the MnWO4 / ZnIn2S4 heterojunction serves as a catalyst, the separation efficiency of current carriers can be further improved, and it is obtained through experiments that the composite material has high hydrogen yield and good stability when being used for photocatalytic water splitting. The method is green and environment-friendly, simple, convenient to operate and low in material preparation cost, conforms to the green and environment-friendly concept advocated at present, and has a wide application market prospect.

The invention discloses a preparation method of a rare earth element doped nickel-based selenide nano-material and application of the rare earth element doped nickel-based selenide nano-material in electro-catalysis water full-hydrolysis reaction. According to the method, nickel salt, cerium salt, selenium dioxide and potassium chloride are prepared into electrolyte, and the electrolyte is subjected to electro-deposition on a foamed nickel substrate to obtain Ce-doped Ni0.85Se nanoparticles growing on foamed nickel. The crystal structure and electron distribution of Ni0.85Se are optimized by doping trace rare earth element cerium, so that the HER and OER performances of the Ni0.85Se are greatly improved. The prepared catalyst is self-supporting closely-packed nanoparticles, the formed amorphous structure is easy to expose more active sites, the catalyst has good electrocatalytic hydrogen evolution and oxygen evolution performance under alkaline conditions, the overpotential in electrocatalysis of nickel-based selenide is greatly reduced, and the electrocatalytic performance of nickel-based selenide is improved. And excellent electro-catalytic activity is shown in electro-catalytic water full hydrolysis. And the self-supporting electrode is not easy to fall off due to generation of bubbles in the reaction process, so that the working stability of the catalyst is improved.

The invention belongs to the technical field of all-vanadium redox flow battery electrodes, and discloses a graphite felt electrode for a vanadium battery and a preparation method and application of the graphite felt electrode. Preparing a spinel composite graphite felt; preparing a spinel inlaid perovskite composite graphite felt electrode; preparing a composite graphite felt electrode; the nano petal-shaped spinel composite perovskite nanospheres are synthesized by adopting an electro-deposition and sol-gel method, the structure is stable, the effective active area is increased, the oxidation reduction capacity of vanadium is catalyzed, the reaction energy barrier is reduced, the precipitation amount of oxygen and hydrogen in an electrolyte is effectively reduced, the oxygen evolution / hydrogen evolution side reaction is inhibited, the utilization rate of the electrolyte is improved, and the service life of the electrolyte is prolonged. And the energy loss generated by side reaction during battery operation is reduced.