阅读说明：本技术 一种表面掺杂修饰MoS2的CoS纳米线催化剂的制备方法和应用 (Surface doping modification MoS2Preparation method and application of CoS nanowire catalyst ) 是由 何元纯 王妍 于 2020-09-19 设计创作，主要内容包括：本发明涉及纳米结构析氢反应催化剂技术领域,特别涉及一种表面掺杂修饰MoS_2的CoS纳米线催化剂的制备方法和应用。以碳布为衬底,利用水热或溶剂热的合成方法,将CoS纳米线负载于碳布上,然后将MoS_2纳米片负载于CoS纳米线上,得到纳米线加纳米片的复合纳米阵列结构,CoS@CC+MoS_2。本发明选择在碳布表面上生长CoS纳米线,碳布经过亲水处理后拥有良好的导电性以及多种优良的电化学性能。通过负载纳米片结构的MoS_2进行结构的改良,从而对催化剂材料的表面进行改性,提高反应活性并实现高效电解水析氢。(The invention relates to the technical field of nano-structure hydrogen evolution reaction catalysts, in particular to a surface-doped modified MoS 2 The preparation method and the application of the CoS nanowire catalyst. Using carbon cloth as a substrate, loading CoS nanowires on the carbon cloth by using a hydrothermal or solvothermal synthesis method, and then loading MoS 2 Loading nano-sheets on the CoS nano-wires to obtain a nano-wire and nano-sheet composite nano-array structure, CoS @ CC + MoS 2 . The invention selects the CoS nanowire growing on the surface of the carbon cloth, and the carbon cloth has good conductivity after hydrophilic treatmentAnd various excellent electrochemical properties. MoS by loading nanosheet structure 2 The structure is improved, so that the surface of the catalyst material is modified, the reaction activity is improved, and the efficient electrolysis of water for hydrogen evolution is realized.)

1. Surface doping modification MoS₂The preparation method of the CoS nanowire catalyst is characterized by comprising the following steps: using carbon cloth as a substrate, loading CoS nanowires on the carbon cloth by using a hydrothermal or solvothermal synthesis method, and then loading MoS₂Loading nano-sheets on the CoS nano-wires to obtain a nano-wire and nano-sheet composite nano-array structure, CoS @ CC + MoS₂。

2. The surface-doped modified MoS of claim 1₂The preparation method of the CoS nanowire catalyst is characterized by comprising the following preparation steps:

1) selecting a substrate and pretreating to remove impurities on the surface of the substrate and improve the hydrophilicity of the substrate;

2) preparation of precursor CoS nanowire: dissolving inorganic metal cobalt salt in water, mixing the inorganic metal cobalt salt with urea to prepare a solution, reacting for a period of time at a certain temperature and pressure to generate cobaltosic oxide nanowires on a substrate, selecting a proper sulfur source, vulcanizing the cobaltosic oxide nanowires at the same temperature, cleaning, carrying out ultrasonic treatment for several seconds, and drying to obtain CoS nanowires loaded on the substrate, namely CoS @ CC;

3)MoS₂preparing a nano sheet: dissolving ammonium molybdate tetrahydrate and thiourea in water to prepare a solution, stirring vigorously, reacting for a period of time at a certain temperature and pressure to obtain a black solution, cleaning, and drying to obtain MoS₂Nanosheets;

4) preparation of CoS @ CC + MoS₂: the prepared MoS₂Dispersing the nanosheets in an organic solvent, placing CoS @ CC in the solution after ultrasonic dispersion, and reacting for a plurality of hours at a certain temperature by adopting a solvothermal method to obtain a nanosheet and nanowire structure with a composite surface, wherein CoS @ CC + MoS₂。

3. Surface doped modified MoS according to claim 2₂The preparation method of the CoS nanowire catalyst is characterized by comprising the following steps: the substrate is hydrophilic carbon cloth;

the pretreatment method of the substrate in the step 1) comprises the following steps of soaking the carbon cloth in a mixed solution of nitric acid, sulfuric acid and water, wherein the volume ratio of the nitric acid to the sulfuric acid to the water is as follows: sulfuric acid: soaking for 24 hours in water at a ratio of 1:1: 10; then respectively soaking the carbon cloth in acetone, ethanol and deionized water, and ultrasonically cleaning for 10 minutes respectively; finally, the treated carbon cloth is placed in an oven at 60 ℃ for drying.

4. Surface doped modified MoS according to claim 2₂The preparation method of the CoS nanowire catalyst is characterized in that the inorganic metal cobalt salt in the step 2) is selected from cobalt chloride hexahydrate; the sulfur source is selected from sodium sulfide nonahydrate; the reaction temperature for synthesizing the cobaltosic oxide is 90 ℃ and the time is 8 hours; the reaction temperature of the cobaltosic oxide sulfide is 90 ℃ and the reaction time is 16 hours.

5. Surface doped modified MoS according to claim 2₂The preparation method of the CoS nanowire catalyst is characterized by comprising the following steps: the concentration of the inorganic metal cobalt salt in the step 2) is 10 mM; the urea accounts for 0.42 wt% of the total mass of the inorganic metal cobalt salt and the urea.

6. Surface doped modified MoS according to claim 2₂The preparation method of the CoS nanowire catalyst is characterized by comprising the following steps: the concentration of the sulfur source in the step 2) is 10 mM; the reaction vessel is a reaction kettle.

7. Surface doped modified MoS according to claim 2₂The preparation method of the CoS nanowire catalyst is characterized by comprising the following steps: the organic solvent in the step 4) is selected from diethylenetriamine.

8. The surface of claim 2Doping modified MoS₂The preparation method of the CoS nanowire catalyst is characterized by comprising the following steps: MoS in the step 4)₂The molar ratio to CoS attached to the substrate is 1:1 or 1: 10.

9. Surface doped modified MoS according to claim 2₂The preparation method of the CoS nanowire catalyst is characterized by comprising the following steps: and 4) coating RTV silicon rubber on the substrate after the step 4).

10. Surface doping modification MoS₂The use of a CoS nanowire catalyst of (a), prepared according to the method of any one of claims 1-9, characterized in that: the CoS @ CC + MoS₂The catalyst is used as a hydrogen evolution catalyst for improving the efficiency of hydrogen evolution of electrolyzed water.

Technical Field

The invention relates to the technical field of nano-structure hydrogen evolution reaction catalysts, in particular to a surface-doped modified MoS₂The preparation method and the application of the CoS nanowire catalyst.

Background

Along with the continuous progress of human society, the scientific technology and material living standard which are closely related to us are continuously improved, and the demand of energy sources is increased day by day, so that the energy crisis and the environmental problems caused by the energy sources are not realized on the converter and the converter. At present, the dominance force of energy structures in China is still traditional fossil fuels such as coal, petroleum, natural gas and the like, and the consumption of non-renewable energy sources can not only generate a large amount of polluting gases, but also aggravate the greenhouse effect, so that the active research and development of renewable efficient clean energy sources are imperative. To date, sustainable energy sources that are favored are: solar energy, wind energy, water energy, geothermal energy, tidal energy, nuclear energy, biological energy and the like, and the defects in the united states are that the novel energy sources have intermittent time and space and cannot ensure long-time stable output, so that hydrogen energy is widely concerned by researchers.

Hydrogen is regarded as the most potential environment-friendly energy carrier in the 21 st century, and compared with other energy sources, hydrogen energy is superior in the following aspects: (1) the storage capacity of hydrogen is large; (2) the hydrogen energy is green clean environment-friendly energy, and the product after the combustion of the hydrogen and the oxygen is water without generating sulfur dioxide, carbon dioxide and other polluting gases; (3) the energy of hydrogen energy is relatively higher. More importantly, Hydrogen can be obtained by utilizing a Hydrogen Evolution Reaction (HER), and the method has different performances under the participation of different catalysts, so that the selection of the high-efficiency catalyst is very important. At present, the catalyst widely studied is mainly transition metal compounds, such as oxides, sulfides, selenides, carbides, phosphides and the like, wherein the oxygen group metal compound plays an important role in the field of catalysis due to the characteristics of superior structure, easy preparation and the like. Different structures exhibit different performance in electrolyzing water. At present, the main methods for improving the performance of the catalyst are to increase the conductivity of the catalyst, compound the structure, construct the active sites of the electrolyzed water and the like.

CoS and MoS in transition metal sulfide₂Is considered to be a very potential catalyst, the two-dimensional lattice structure of the catalyst is similar to that of graphene, the specific surface area of a CoS nanowire structure is large, and the catalyst can be prepared for electrolyzing waterHydrogen provides a relatively rich active site, thus making the efficiency of electrocatalytic energy conversion relatively ideal. However, the surface active sites of the catalyst still need to be improved so as to prepare a catalyst with higher reaction activity for water decomposition and hydrogen evolution.

Disclosure of Invention

Aiming at the defects in the prior art, the technical problem to be solved by the invention is to provide a method for improving hydrogen production by water electrolysis by utilizing a strategy of complementation of advantages of nanowires and nanosheets, and a uniform composite nanostructure array is prepared on carbon cloth by utilizing a hydrothermal/solvothermal synthesis method, so that the stability and improvement of the structure are realized, and the efficiency of hydrogen evolution by water electrolysis is improved.

The technical scheme adopted by the invention for realizing the purpose is as follows: surface doping modification MoS₂The preparation method of the CoS nanowire catalyst comprises the steps of taking carbon cloth as a substrate, utilizing a hydrothermal or solvothermal synthesis method to load CoS nanowires on the carbon cloth, and then loading MoS nanowires on the carbon cloth₂Loading nano-sheets on the CoS nano-wires to obtain a nano-wire and nano-sheet composite nano-array structure, CoS @ CC + MoS₂。

Further, the preparation steps are as follows:

1) selecting a substrate and pretreating to remove impurities on the surface of the substrate and improve the hydrophilicity of the substrate;

2) preparation of precursor CoS nanowire: dissolving inorganic metal cobalt salt in water, mixing the inorganic metal cobalt salt with urea to prepare a solution, reacting for a period of time at a certain temperature and pressure to generate cobaltosic oxide nanowires on a substrate, selecting a proper sulfur source, vulcanizing the cobaltosic oxide nanowires at the same temperature, cleaning, carrying out ultrasonic treatment for several seconds, and drying to obtain CoS nanowires loaded on the substrate, namely CoS @ CC;

3)MoS₂preparing a nano sheet: dissolving ammonium molybdate tetrahydrate and thiourea in water to prepare a solution, stirring vigorously, reacting for a period of time at a certain temperature and pressure to obtain a black solution, cleaning, and drying to obtain MoS₂Nanosheets;

4) preparation of CoS @ CC + MoS₂: the prepared MoS₂The nano-sheets are dispersed in an organic solvent,after ultrasonic dispersion, placing CoS @ CC into a solution, and reacting for a plurality of hours at a certain temperature by adopting a solvothermal method to obtain a surface composite nanosheet and nanowire structure, wherein CoS @ CC + MoS₂。

Further, the substrate is hydrophilic carbon cloth;

the pretreatment method of the substrate in the step 1) comprises the following steps of soaking the carbon cloth in a mixed solution of nitric acid, sulfuric acid and water, wherein the volume ratio of the nitric acid to the sulfuric acid to the water is as follows: sulfuric acid: soaking for 24 hours in water at a ratio of 1:1: 10; then respectively soaking the carbon cloth in acetone, ethanol and deionized water, and ultrasonically cleaning for 10 minutes respectively; finally, the treated carbon cloth is placed in an oven at 60 ℃ for drying.

Further, the inorganic metal cobalt salt in the step 2) is selected from cobalt chloride hexahydrate; the sulfur source is selected from sodium sulfide nonahydrate; the reaction temperature for synthesizing the cobaltosic oxide is 90 ℃ and the time is 8 hours; the reaction temperature of the cobaltosic oxide sulfide is 90 ℃ and the reaction time is 16 hours.

Further, the concentration of the inorganic metal cobalt salt in the step 2) is 10 mM; the urea accounts for 0.42 wt% of the total mass of the inorganic metal cobalt salt and the urea.

Further, the concentration of the sulfur source in the step 2) is 10 mM; the reaction vessel is a reaction kettle.

Further, the organic solvent in the step 4) is selected from diethylenetriamine.

Further, MoS in the step 4)₂The molar ratio to CoS attached to the substrate is 1:1 or 1: 10.

Further, coating RTV silicon rubber on the substrate after the step 4).

The invention also comprises a surface doping modified MoS₂The CoS @ CC + MoS₂The catalyst is used as a hydrogen evolution catalyst for improving the efficiency of hydrogen evolution of electrolyzed water.

The surface of the invention is doped and modified with MoS₂The preparation method and the application of the CoS nanowire catalyst have the beneficial effects that:

(1) the invention provides a method for synthesizing a composite material, which optimizes the proportion of two materials, and obtains the optimal sample morphology through parameter adjustment, so that the obtained catalyst material has better electro-catalytic performance.

(2) Through hydrophilic treatment of the carbon cloth, hydrothermal/solvent thermal processes and the like for preparing CoS @ CC + MoS2 on the carbon cloth are optimized, and the uniformity and high catalytic performance of compounding the CoS @ CC + MoS2 nano wires and nano sheets on the carbon cloth are ensured.

(3) The method has the advantages of simple required equipment, low cost, convenient operation and good repeatability.

The CoS nanowire grows on the surface of the carbon cloth, and the carbon cloth has good conductivity and various excellent electrochemical properties after hydrophilic treatment. MoS by loading nanosheet structure₂The structure is improved, so that the surface of the catalyst material is modified, the reaction activity is improved, and the efficient electrolysis of water for hydrogen evolution is realized.

Drawings

FIG. 1 shows different ratios of CoS @ CC + MoS in an embodiment of the present invention₂Scanning Electron Microscope (SEM) images of nanowire and nanosheet structures;

FIG. 2 shows Co in an embodiment of the present invention₃O₄Scanning Electron Microscope (SEM) images of @ CC nanowire structures;

FIG. 3 shows Co in an embodiment of the present invention₃O₄An Energy Dispersive Spectroscopy (EDS) plot of the @ CC nanowire structure;

FIG. 4 is a Scanning Electron Microscope (SEM) image of a CoS @ CC nanowire structure in an embodiment of the invention;

FIG. 5 is a graph of Energy Dispersive Spectroscopy (EDS) of a CoS @ CC nanowire structure in an embodiment of the present invention;

FIG. 6 shows an embodiment of the invention in which MoS₂Scanning Electron Microscope (SEM) images of the nanosheet structure;

FIG. 7 shows different reaction times CoS @ CC + MoS in DETA according to an embodiment of the present invention₂A hydrogen evolution performance (HER) profile of the composite;

FIG. 8 shows different ratios of CoS @ CC + MoS according to an embodiment of the present invention₂Hydrogen evolution performance (HER) profile of the composite.

Detailed Description

The invention is further explained in detail with reference to the drawings and the specific embodiments;

example 1:

surface doping modification MoS₂The preparation method of the CoS nanowire catalyst comprises the steps of taking carbon cloth as a substrate, utilizing a hydrothermal or solvothermal synthesis method to load CoS nanowires on the carbon cloth, and then loading MoS nanowires on the carbon cloth₂Loading nano-sheets on the CoS nano-wires to obtain a nano-wire and nano-sheet composite nano-array structure, CoS @ CC + MoS₂。

The preparation steps are as follows:

1) selecting a substrate and pretreating to remove impurities on the surface of the substrate and improve the hydrophilicity of the substrate;

2) preparation of precursor CoS nanowire: dissolving inorganic metal cobalt salt in water, mixing the inorganic metal cobalt salt with urea to prepare a solution, reacting for a period of time at a certain temperature and pressure to generate cobaltosic oxide nanowires on a substrate, selecting a proper sulfur source, vulcanizing the cobaltosic oxide nanowires at the same temperature, cleaning, carrying out ultrasonic treatment for several seconds, and drying to obtain CoS nanowires loaded on the substrate, namely CoS @ CC;

3)MoS₂preparing a nano sheet: dissolving ammonium molybdate tetrahydrate and thiourea in water to prepare a solution, stirring vigorously, reacting for a period of time at a certain temperature and pressure to obtain a black solution, cleaning, and drying to obtain MoS₂Nanosheets;

4) preparation of CoS @ CC + MoS₂: the prepared MoS₂Dispersing the nanosheets in an organic solvent, placing CoS @ CC in the solution after ultrasonic dispersion, and reacting for a plurality of hours at a certain temperature by adopting a solvothermal method to obtain a nanosheet and nanowire structure with a composite surface, wherein CoS @ CC + MoS₂。

The substrate is hydrophilic carbon cloth;

the pretreatment method of the substrate in the step 1) comprises the following steps of soaking the carbon cloth in a mixed solution of nitric acid, sulfuric acid and water, wherein the volume ratio of the nitric acid to the sulfuric acid to the water is as follows: sulfuric acid: soaking for 24 hours in water at a ratio of 1:1: 10; then respectively soaking the carbon cloth in acetone, ethanol and deionized water, and ultrasonically cleaning for 10 minutes respectively; finally, the treated carbon cloth is placed in an oven at 60 ℃ for drying.

The inorganic metal cobalt salt in the step 2) is selected from cobalt chloride hexahydrate; the sulfur source is selected from sodium sulfide nonahydrate; the reaction temperature for synthesizing the cobaltosic oxide is 90 ℃ and the time is 8 hours; the reaction temperature of the cobaltosic oxide sulfide is 90 ℃ and the reaction time is 16 hours.

The concentration of the inorganic metal cobalt salt in the step 2) is 10 mM; the urea accounts for 0.42 wt% of the total mass of the inorganic metal cobalt salt and the urea.

The concentration of the sulfur source in the step 2) is 10 mM; the reaction vessel is a reaction kettle.

The organic solvent in the step 4) is selected from diethylenetriamine.

MoS in the step 4)₂The molar ratio to CoS attached to the substrate is 1:1 or 1: 10.

Coating RTV silicon rubber on the substrate after the step 4) to ensure that the surface area of the sample participating in the reaction is as close to 1cm as possible²Wherein, the RTV silicon rubber can effectively prevent the electrolyte in the electrolytic cell from seeping out of the working range of the sample and even seeping into the electrode clamp.

The invention also comprises a surface doping modified MoS₂The CoS @ CC + MoS₂The catalyst is used as a hydrogen evolution catalyst for improving the efficiency of hydrogen evolution of electrolyzed water.

In the invention, CV (cyclic voltammetry) test is firstly carried out on a sample, so that the contingency of the experiment is reduced, and the HER electrochemical water decomposition performance of the material is more stable. CV voltage range of-0.075V to 1.025V (vs. RHE), scan speed of 100m V/s, interval voltage of 0.001V, and cycle number of 10. And then, carrying out HER performance test, and selecting an LSV (Linear Sweep Voltammetry) mode in an electrochemical workstation to test the hydrogen evolution reaction performance of the sample, wherein the electrolyte used for the test is a 1mol/L KOH solution.

Example 2:

surface doping modification MoS₂The preparation method of the CoS nanowire catalyst comprises the following preparation steps:

1) selection and pretreatment of substrates

A Cetech carbon cloth WOS1009 with high relative hydrophilicity was selected as a substrate and cut into a rectangle with a size of 40mm × 20mm × 0.33 mm. And then carrying out hydrophilic treatment on the substrate, specifically soaking the carbon cloth in a mixed solution of nitric acid, sulfuric acid and water, wherein the volume ratio of the nitric acid to the sulfuric acid to the water is as follows: sulfuric acid: soaking for 24 hours in water at the ratio of 1:1:10 to remove oxides and other impurities on the surface of the substrate; then respectively soaking the carbon cloth in acetone, ethanol and deionized water, and ultrasonically cleaning for 10 minutes respectively; finally, the treated carbon cloth is dried in an oven at 60 ℃.

2) Preparation of cobalt sulfide nanowires

Selecting a 50mL explosion-proof hydrothermal reaction kettle as a reaction container, and weighing 0.1538g of urea and 10mM CoCl prepared in advance by using an analytical balance₂·6H₂And uniformly mixing O35 mL of solution to obtain a transparent solution, transferring the solution to a 50mL reaction kettle lining, obliquely placing the treated carbon cloth (40mm multiplied by 20mm) in the reaction kettle lining as much as possible, preserving the heat at 90 ℃ for 8 hours, cooling to room temperature, preparing a cobaltosic oxide precursor on the carbon cloth, and then drying in an oven at 60 ℃.

Then sulfurizing to prepare a certain amount of 10mM Na₂40mL of S.9H 2O solution is weighed into a reaction kettle lining, and Co prepared in advance is put into the reaction kettle lining₃O₄@ CC, keeping the temperature at 90 ℃ for 16 hours, and naturally cooling to room temperature to obtain the CoS @ CC nanowire.

FIGS. 2 to 5 are each Co₃O₄The Scanning Electron Microscope (SEM) picture and the corresponding Energy Dispersion Spectrum (EDS) picture of the @ CC nanowire and CoS @ CC nanowire structures can show a uniform nanowire array structure.

Wherein in fig. 3, element C accounts for 88.87%; the content of O element is 10.62 percent; the content of Co element is 0.51%.

Wherein in FIG. 5, element C accounts for 65.28%; the content of O element is 22.9 percent; the content of S element is 6.7%; the content of Co element is 5.13%.

3) CoS @ CC nanowire electrochemical testing

A three-electrode system is adopted to carry out electrochemical performance test on a sample, the prepared sample is used as a working electrode, Pt is used as a counter electrode, Ag/AgCl is used as a reference electrode, cyclic voltammetry scanning is firstly carried out on the sample, the test conditions are that the CV voltage range is-0.075V to 1.025V (vs. RHE), the scanning speed is 100m V/s, the interval voltage is 0.001V, and the cycle number is 10 times. And then subjected to a hydrogen evolution performance (HER) test.

4) Preparation of molybdenum disulfide nanosheet

Selecting a 50mL explosion-proof hydrothermal reaction kettle as a reaction vessel, weighing 1.2360g (1mmol) of ammonium molybdate tetrahydrate and 2.2840g (30mmol) of thiourea in 35mL deionized water by using an analytical balance, stirring vigorously for 30 minutes, transferring the solution into a 50mL reaction kettle lining, preserving heat at 220 ℃ for 10 hours, cooling to room temperature to obtain a black solution, washing with deionized water and ethanol respectively for three times, and then placing the obtained powder in an oven at 60 ℃ for drying.

FIG. 6 shows MoS₂The Scanning Electron Microscope (SEM) picture of the nano-sheet structure shows a uniform nano-sheet array structure.

5)[email protected]+MoS₂Preparation of nanowire and nanosheet composites

Using Diethyltriamine (DETA) as solvent according to CoS: MoS₂1:1 according to CoS: MoS₂Dispersing the prepared molybdenum disulfide at the ratio of 10:1, putting the prepared CoS @ CC into a solution after ultrasonic dispersion, and reacting at 120 ℃ for 2h/4h/8h/16h/32h by adopting a solvothermal method to obtain the surface composite nanowire and nano-sheet structure CoS @ CC + MoS₂。

6)[email protected]+MoS₂Electrochemical testing of nanowire and nanosheet composites

A three-electrode system is adopted to carry out electrochemical performance test on a sample, the prepared sample is used as a working electrode, Pt is used as a counter electrode, Ag/AgCl is used as a reference electrode, cyclic voltammetry scanning is firstly carried out on the sample, the test conditions are that the CV voltage range is-0.075V to 1.025V (vs. RHE), the scanning speed is 100m V/s, the interval voltage is 0.001V, and the cycle number is 10 times. And then subjected to a hydrogen evolution performance (HER) test. FIG. 7 shows the different reaction times CoS @ CC + MoS in DETA₂Figure 8 is a graph of hydrogen evolution performance (HER) of the composite material with different ratios of CoS @ CC + MoS₂Hydrogen evolution Performance (HER) diagram of composite materials(ii) a FIG. 1 shows different ratios of CoS @ CC + MoS₂Scanning Electron Microscope (SEM) images of nanowire and nanosheet structures.

The preparation method has the advantages that efficient hydrogen production through water electrolysis is realized, on the premise that a proper high-catalytic-activity electrode material is found, transition metal sulfide CoS is abundant in reserves, low in price and easy to obtain, and attracts great attention among a plurality of catalytic materials, the CoS nanowire has a linear structure, so that the CoS nanowire has a large specific surface area and provides a large number of reaction active sites for hydrogen production through water electrocatalytic decomposition, and CoS shows good catalytic activity. But the catalytic efficiency is still not ideal due to the single material obtained. It is known that sulfur has a lower electronegativity than oxygen, metal sulfides have a slightly better conductivity than oxides, and transition metal sulfides have a better electrochemical performance than oxides. For this, we chose MoS₂Surface doping modification is carried out on the mixture, MoS₂The quasi-two-dimensional material has good flexibility and large specific surface area, and also has standard MX₂The structure is characterized in that Mo atoms are used as the center in the middle and are coordinated with surrounding S atoms to form an S-Mo-S alternate structure, the edge atoms S of the molybdenum disulfide nanosheet layered structure are active sites for hydrogen production through water electrolysis, and through the compounding of two metal sulfide materials, the active sites on the surface of the material can be effectively increased, the charge transfer rate is accelerated, the advantage complementation of different morphological structures is realized, and the electro-catalysis hydrogen evolution efficiency is improved.

As can be seen from FIG. 1, CoS @ CC + MoS prepared by the invention₂The nano wire and nano sheet composite material is uniform and regular, the specific surface area is larger, the molybdenum disulfide nano sheets are uniformly and completely coated on the outer layer of the cobalt sulfide nano wire, the collapse and the breakage of the structure of the cobalt sulfide nano wire are effectively inhibited, the flexibility of the material is increased, and the integral stability of the structure is improved.

The experimental methods used in the above examples are all conventional methods unless otherwise specified.

The materials and reagents used in the above examples were commercially available or synthesized from commercially available raw materials, unless otherwise specified.

The above embodiments are only for illustrating the technical concept and features of the present invention, and the purpose thereof is to enable those skilled in the art to understand the contents of the present invention and implement the present invention accordingly, and not to limit the protection scope of the present invention accordingly. All equivalent changes or modifications made in accordance with the spirit of the present disclosure are intended to be covered by the scope of the present disclosure.