1631 results about "Hydrogen evolution" patented technology

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.

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 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 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.

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 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 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 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 relates to a catalyst for the hydrogen evolution reaction (HER) and methods for using the catalyst in a water-splitting process. A hydrogen evolution reaction (HER) electrocatalyst, and a method and use for preparing a HER electrocatalyst are disclosed. The method comprises the step of forming a two-dimensional electron gas (2DEG) interface at a heterojunction of at least one of two or more alternating layers of a first complex oxide and a second complex oxide, wherein the or each 2DEG interface exhibits a current density, corresponding to an intrinsic hydrogen evolution reaction (HER) activity that renders the 2DEG interface(s) suitable as an HER electrocatalyst for producing hydrogen (H2) from a water-based electrolyte by water electrolysis.

The invention discloses a zinc-bromine flow battery electrolyte, a negative electrode cosolvent and a preparation method thereof, and belongs to the technical field of electrochemical energy storage, the negative electrode cosolvent of the zinc-bromine flow battery electrolyte is a carboxyl-containing butenoic acid substance, the butenoic acid substance is used as the cosolvent, and zinc is induced to preferentially deposit on a (002) plane by modifying a solid-liquid interface, so that the zinc-bromine flow battery electrolyte is obtained. And the deposition process of zinc is converted from an irregular form which tends to form a dendritic crystal shape and a moss shape into a deposition layer which tends to form a flat and compact deposition layer which is parallel to the substrate. The highly uniform zinc deposition fundamentally and effectively inhibits the formation and growth of zinc dendrites, and greatly improves the stability of the negative electrode and the cycle life of the battery. Chlorides improve ionic conductivity to reduce internal resistance, and sodium acetate buffer inhibits hydrogen evolution on stable pH; and synergistic optimization of positive and negative components ensures efficient reaction. And moreover, the raw materials are easy to obtain, the preparation is simple and convenient, the industrialization threshold is reduced, and the large-scale energy storage requirement is met.

The invention provides a synchronous electrochemical test and hydrogen evolution test experimental device and method, and belongs to the field of metal corrosion research. The experimental device provided by the invention comprises a hydrogen evolution test module, an electrochemical test module and a control system module, and the control system module controls the hydrogen evolution test module and the electrochemical test module to work through circuit connection. By combining the hydrogen evolution test and the electrochemical test, the automatic accurate measurement of the hydrogen evolution amount in the metal corrosion process can be realized, the measurement of the corrosion rate, the corrosion potential and the charge transfer amount in the oxidation-reduction reaction can also be realized, and the problems of poor sustainability and low precision of the traditional hydrogen evolution test method are avoided; the hydrogen evolution test data and the electrochemical test data are automatically obtained while one-time sample preparation is realized.

The invention relates to the technical field of catalysts, in particular to an alkaline electrolytic water hydrogen evolution catalyst of a Pt-Co core-shell nanocluster loaded VN / CNT composite carrier, which comprises a composite carrier and a core-shell nanocluster loaded on the composite carrier, the composite carrier is a VN / CNT composite carrier, and the core-shell nano-cluster is a Pt-Co core-shell nano-cluster; the Pt-Co core-shell nano-cluster takes Pt as a core and Co as a shell, and the particle size of the core-shell is 1-15 nm; the VN / CNT composite carrier comprises CNT and VN nanoparticles loaded on the CNT, and the mass fraction of VN is 5%-40%. In the Pt-Co core-shell structure, the Co shell layer optimizes the d band center of Pt through an electronic effect, and reduces the adsorption energy barrier of H *; meanwhile, the Co shell serves as a co-catalyst, dissociation of H2O under the alkaline condition is remarkably promoted, and compared with a single Pt catalyst, the activity is improved by 30% or above under the same Pt dosage.

The invention relates to the technical field of chemical catalysis, and particularly discloses a covalent organic framework material loaded bimetallic monatomic electrocatalyst and a preparation method and application thereof, the catalyst comprises a carrier and atomic-scale dispersed metal diatomic active sites; the atomic-scale dispersed metal diatomic active sites are anchored in the carrier through a simple post-impregnation method; the carrier is a triazinyl covalent organic framework; a coordination structure is formed between the atomic-scale dispersed metal diatomic active sites and the carrier through a nitrogen-metal-chlorine bridging structure; the diatom-dispersed difunctional electrocatalyst has good overall water decomposition performance, under the condition of 1M KOH, the overpotential of hydrogen evolution reaction is 39.3 mV at 10 mA cm <-2 >, the overpotential of oxygen evolution reaction is 251.2 mV at 10 mA cm <-2 >, the synthesis process is simple and easy to implement, the preparation cost is low, and the diatom-dispersed difunctional electrocatalyst has industrial production and application prospects.

This invention relates to the field of alkaline water electrolysis for hydrogen production, and discloses a water electrolysis hydrogen evolution catalyst, its preparation method, and a method for water electrolysis to produce hydrogen. The catalyst contains Ru, Co, Ni, C, and N; wherein C exists in the catalyst in the form of carbon nanotubes; the Ru content in the catalyst is 0.1-5 wt%, and the average particle size of Ru is 2-5 nm. This invention uses a carbon nanotube composite structure generated by ZIF pyrolysis as a support, which improves the charge transfer capacity by increasing the Ru loading and dispersion. Furthermore, the synergistic effect of Ru with Co and Ni effectively enhances the catalytic hydrogen evolution activity of the Ru-Co-Ni water electrolysis hydrogen evolution catalyst.

The invention relates to a liquid flow battery electrolyte storage device, and relates to the technical field of liquid flow battery electrolytes.The liquid flow battery electrolyte storage device comprises a tank shell and a heat exchange pipe, a spiral storage pipe barrel arranged in the vertical direction is arranged in the tank shell, electrolyte is arranged in the storage pipe barrel, the storage pipe barrel is connected with a liquid pump, the heat exchange pipe is spiral, and the heat exchange pipe is connected with the liquid pump. The storage pipe barrel is arranged vertically in a spiral mode and arranged outside the storage pipe barrel in a sleeving mode, heat exchange liquid is arranged in the heat exchange pipe, the heat exchange pipe is connected with a liquid supply circulating device, the flowing direction of the electrolyte is opposite to that of the heat exchange liquid, the storage pipe barrel is vertically arranged in a spiral mode, the electrolyte in the storage pipe barrel can form ordered layering in the storage pipe barrel, and therefore the heat exchange effect is improved. According to the utility model, the generation of a flowing dead zone is avoided, the occurrence of a side reaction, namely a hydrogen evolution reaction, caused by the mixing of two different ions is also reduced, the heat exchange area is increased, countercurrent flow heat exchange is realized, and the heat exchange efficiency of the device is further ensured.

The invention provides an Au nanocluster-Cu monatomic / titanium dioxide photocatalyst as well as a preparation method and application thereof, and belongs to the technical field of photocatalysis. According to the invention, the Cu monatomic atom is used as a catalyst for hydrogen evolution reaction, the Cu monatomic atom and the Au nano-cluster are loaded at the same time, the Cu monatomic atom can be used as an electron transport bridge to regulate the electronic structure of the Au nano-cluster, the synergistic effect of the Cu monatomic atom and the Au nano-cluster is realized, the catalytic activity is regulated and controlled together, and efficient series connection of multi-step reaction is realized; therefore, the product selectivity can be accurately regulated and controlled; the catalytic oxidation reaction can be dynamically adjusted through carrier mediation or direct contact by virtue of the electron interaction between the Cu monatomic and the Au nano-cluster, so that the electron distribution in the catalytic process is favorably optimized, the reaction energy barrier of C-C bond breakage and hydroxymethyl oxidation is regulated and controlled, and the dynamic performance of generating GA and hydrogen through photocatalytic oxidation of EG is improved.

This application relates to the field of hydrogel electrolyte technology, specifically disclosing a modified sodium alginate crosslinked hydrogel electrolyte, its preparation method, and its applications. This application reduces environmental toxicity and pollution by introducing modified sodium alginate as a crosslinking agent into the hydrogel electrolyte. The interaction between sodium alginate and zinc ions inhibits zinc dendrite formation, regulates the interfacial growth between the negative electrode and the electrolyte, and thus extends battery life; it also has a certain inhibitory effect on hydrogen evolution reaction. This application can prepare the modified sodium alginate crosslinked hydrogel electrolyte using a simple free radical polymerization method. Furthermore, compared to conventional aqueous batteries, the hydrogel electrolyte can better control the interfacial growth of the positive and negative electrodes.

The invention discloses a Ce-doped CoP / NiCoP-coated NM self-supporting structure electrode and a preparation method and application thereof, the electrode takes a pretreated nickel net as a conductive substrate, a two-step method combining pulse electrodeposition and constant potential deposition is adopted, a compact NiCoP bottom layer and a Ce-doped CoP outer layer are constructed in sequence, and a CoP / NiCoP heterojunction structure with a three-dimensional coralline open morphology is formed. The method is mild in process, green, simple and convenient, and a traditional high-temperature phosphating step is abandoned. The prepared self-supporting electrode combines the charge regulation advantage of a heterojunction interface, the Ce-doped electronic structure optimization effect and the mass transfer advantage of a three-dimensional porous structure, so that the self-supporting electrode has extremely high hydrogen evolution catalytic activity, strong bonding force with a substrate and excellent long-period operation stability.

A nanocomposite catalyst for use as an electrode in water electrolysis includes a cobalt triazole (Co-Tri) metal-organic framework (MOF), carbon quantum dots (CQDs), carbon nanosheets (CNs), and an ionically conductive polymer binder. The mass ratio of the nanocomposite catalyst includes cobalt triazole metal-organic framework to the carbon quantum dots is in the range of 1:2 to 1:4, and the mass ratio of the cobalt triazole metal organic framework to the carbon nanosheets mass ratio is in the range of 1:4 to 1:6. The nanocomposite catalyst includes current density less than or equal to (≤) −5 milliampere per centimeter square (mA·cm−2) at an applied potential of −100 millivolts (mV) when catalyzing the hydrogen evolution reaction (HER) in water electrolysis.

The invention discloses a composite cathode and anode plate made of a lead-carbon composite material, the composite cathode and anode plate comprises a current collector, a transition layer and an active layer which are compounded in sequence, the transition layer tightly coats the outer surface of the current collector, the active layer tightly coats the outer surface of the transition layer, and the composite cathode and anode plate is prepared by the following method: S1, preparing the composite cathode and anode plate; raw material pretreatment: placing the carbon material in a vacuum oven; according to the invention, the structural design of the composite negative plate and the preparation process are integrated, so that accurate matching of the raw material ratio and the process parameters is realized, and many defects of the traditional electrode are effectively solved; the three-layer gradient structure improves the interface bonding force, and delamination is avoided; the optimized raw material system and the preparation process have a synergistic effect, so that the hydrogen evolution overpotential is remarkably improved, the internal resistance is reduced, the cycle life is prolonged, the low-temperature performance is improved, the energy density is improved, and a reliable technical scheme is provided for the application of the lead-acid storage battery in the high-end field.

A surface-modified catalyst, a multilayer cathode and a system for the electrochemical reduction of carbon dioxide in an acidic medium releasing protons are described. More particularly, the surface-modified catalyst, the multilayer cathode and the system comprise least one heterocyclic organic molecule preventing protons from accessing an active site on a surface of the cathode catalyst material to decrease an hydrogen evolution reaction, as compared to the absence of said heterocyclic organic molecule. The use of the surface-modified catalyst, the multilayer cathode and the system for the production of multicarbon products as well as their processes of manufacturing are also described. Finally, also described are methods for electrochemical production of a multicarbon product using the multilayer cathode and the system.

The invention relates to a preparation method of an in-situ growth neutral gel electrolyte membrane regulated and controlled by ethanolamine and application of the neutral gel electrolyte membrane in negative electrode protection of an aqueous zinc ion battery. The gel is promoted to form a film on the surface of a zinc plate by utilizing the crosslinking effect of ethanolamine, acrylamide and 2-acrylamide-2-methylpropanesulfonic acid and the strong bonding effect of ethanolamine and the zinc plate. The membrane can improve the problems of low ion transfer rate, high free water molecule content and high activity of the traditional gel electrolyte, effectively inhibit the generation of hydrogen evolution reaction, and improve the ion transfer number, thereby improving the stability of the negative electrode and the intestinal circulation performance of the battery. The method is simple and safe to operate and shows excellent electrochemical performance, and the invention provides the method for protecting the negative electrode of the aqueous zinc ion battery.

A hybrid electrochemical device configuration that comprises a first electrode that includes a redox reactive material or an alloy based on a transition metal, a second electrode that includes a multi-functional catalyst to catalyze hydrogen evolution reaction, hydrogen oxidation reaction, and water oxidation reaction at the second electrode, a separator disposed between the first and second electrode, an electrolyte disposed between the first electrode and the second electrode, and a conduit which provides the means to compensate for water loss in the electrolyte during electrochemical device operation. At least one valve is included that connects the electrolyte management system to the conduit system and a valve to connect the gas formed in the electrode to the gas management system. The electrochemical device configurations include several individual devices stacked on top of each other and separated from each other using separation plates.

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 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 provides a hydrated eutectic electrolyte as well as a preparation method and application thereof. The electrolyte comprises water-soluble zinc salt, deionized water and a deep eutectic solution, the deep eutectic solution is formed by mixing zinc perchlorate and a polar deep eutectic solvent and performing deep eutectic crystallization. The electrolyte has the characteristics of low water activity, low freezing point and efficient induction of uniform deposition of zinc, can be compatible with an iodine-loaded positive electrode and can inhibit dissolution of iodine, and the characteristics are beneficial to inhibition of hydrogen evolution reaction, polyiodine shuttling and other side reactions in the battery circulation process, promote uniform deposition of zinc, protect the integrity of an iodine electrode, and improve the electrochemical performance of the battery. The stable operation of the zinc-iodine battery is ensured; the electrolyte is a zinc sulfate solution containing a ZnClO4 / dimethyl sulfoxide deep eutectic solvent, the solution is combined with free water to form a eutectic structure, the eutectic structure participates in construction of a Zn < 2 + > ion solvation shell, extra intramolecular hydrogen bonds are introduced for the electrolyte, meanwhile, hydrogen bonds among water molecules are weakened, so that the internal energy of the electrolyte is enhanced, the freezing point is reduced, and the flowability is improved.

The invention belongs to the technical field of electrode plates, and particularly relates to a high-activity binary alloy hydrogen evolution electrode plate and a preparation process method. The preparation process method comprises the following steps: obtaining a metal nickel electrode substrate and white corundum sand with different particle sizes; carrying out cleaning treatment on the metal nickel initial electrode substrate; the pretreated metal nickel initial base body serves as a working electrode, and sand blasting pretreatment is conducted on a metal nickel electrode base body through white corundum sand; dust removal operation is conducted on the metal nickel electrode base body subjected to sand blasting pretreatment; and spraying binary metal alloy powder on the intermediate hydrogen evolution electrode plate through an atmospheric plasma spraying process to form the high-activity binary alloy hydrogen evolution electrode plate. The whole preparation process method sequentially comprises the steps of cleaning treatment, sand blasting pretreatment, atmospheric plasma spraying, natural cooling and the like, the process method for preparing the electrode plate is optimized, it is guaranteed that the electrode plate has excellent long-time hydrogen evolution stability when the electrode plate is subjected to a hydrogen evolution reaction, and the excellent hydrogen production effect can be achieved.

The invention belongs to the technical field of industrial wastewater purification, and discloses a membrane-free single-tank water electrolysis hydrogen production-electroplating wastewater enrichment coupling method and device, and the method comprises the following steps: injecting a neutral electroplating wastewater mixed solution into a membrane-free single tank; discharging air in the membrane-free single tank, and heating the neutral electroplating wastewater mixed solution to a preset temperature; direct current is firstly introduced into the heated neutral electroplating wastewater mixed solution, so that metal ions in the neutral electroplating wastewater mixed solution migrate to the hydrogen evolution electrode, then the direct current is converted into pulse current, so that the metal ions deposit on the hydrogen evolution electrode, and hydrogen precipitated on the hydrogen evolution electrode is continuously collected; closing the current, taking out the hydrogen evolution electrode and collecting metal ions on the hydrogen evolution electrode; and adding an oxygen evolution catalyst into the membrane-free single tank, starting the magnetic rotor to carry out oxygen evolution reaction, and taking out the oxygen evolution catalyst until bromate in the neutral electroplating wastewater mixed solution is completely reduced. According to the invention, the preparation of high-purity hydrogen and oxygen and the enrichment of metal ions can be realized.

The invention belongs to the technical field of hydrolysis hydrogen production, and particularly relates to a preparation method of a CoPx-CeO2 loaded platinum catalyst with a core-shell structure and application of the CoPx-CeO2 loaded platinum catalyst in seawater electrolysis hydrogen production. A Co (CO3) 0.5 (OH) nanorod precursor is prepared on foamed nickel through a hydrothermal method and then calcined to obtain CoPx, a CeO2 film is electrically deposited to obtain a CoPx-CeO2 composite carrier, and platinum is impregnated and loaded to obtain the CoPx-CeO2-Pt catalyst. The catalyst shows excellent hydrogen evolution catalytic activity in seawater, and the CoPx-CeO2 composite carrier prevents Pt nano-particles from being agglomerated through interaction of metal carriers, so that the atom utilization rate of Pt is increased. Meanwhile, the CeO2 film actively enriches OH <-> in an alkaline electrolyte to construct a local high-alkalinity microenvironment on the surface of the catalyst, Cl <-> in seawater is prevented from getting close to an active site corroding the catalyst through electrostatic repulsion, and the stability and durability of the catalyst are improved.

A preparation method of a high-activity nitrogen-doped carbon-loaded CoRu nano-alloy is used for enhancing pH universal hydrogen evolution, and is characterized by comprising the following steps: dissolving dopamine hydrochloride in an aqueous solution containing H2O2 and CuSO4. 5H2O, and magnetically stirring to form a uniform mixture; and pre-wetting carbon cloth with ethanol, immersing the pre-wetted carbon cloth in the dopamine solution for 10 minutes, taking out the pre-wetted carbon cloth, washing the pre-wetted carbon cloth with deionized water for three times, and carrying out vacuum drying to obtain the polydopamine modified carbon cloth marked as PDA / CC. And immersing the obtained PDA / CC into 20 mL of aqueous solution containing Co (NO3) 2.6 H2O and RuCl3 for 6 hours to realize metal ion adsorption. And washing and drying a sample, and calcining the sample in a tubular furnace at 700 DEG C in an N atmosphere for 2 hours to obtain the self-supporting nitrogen-doped porous carbon-loaded CoRu alloy material which is recorded as CoxRu (at) CN / CC. Through a synthesis strategy based on active ion capture and in-situ carbon thermal reduction, and through construction of a nitrogen-doped carbon cobalt ruthenium alloy nanostructure and a strong metal-carrier synergistic effect, efficient hydrogen overflow and establishment of stable active sites are realized; therefore, the performance bottleneck that high activity and high stability of a traditional electrocatalyst in a wide pH range are difficult to cooperate is broken through.