CN113816425A - MoS2Nitrogen-doped carbon/modified activated carbon sodium ion battery negative electrode material and preparation method thereof - Google Patents

MoS2Nitrogen-doped carbon/modified activated carbon sodium ion battery negative electrode material and preparation method thereof Download PDF

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CN113816425A
CN113816425A CN202111084322.5A CN202111084322A CN113816425A CN 113816425 A CN113816425 A CN 113816425A CN 202111084322 A CN202111084322 A CN 202111084322A CN 113816425 A CN113816425 A CN 113816425A
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activated carbon
modified activated
ion battery
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CN113816425B (en
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许占位
王盈
陆凡宇
刘鑫悦
任宇川
严皓
黄剑锋
杨军
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Shaanxi Coal and Chemical Technology Institute Co Ltd
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Shaanxi University of Science and Technology
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Abstract

The invention discloses a MoS2Nitrogen-doped carbon/modified activated carbon sodium ion battery negative electrode materialFirstly, modifying active carbon by adopting a nitric acid solution water bath heat treatment method to obtain modified active carbon, then synthesizing iron phthalocyanine/modified active carbon by adopting an in-situ solid phase method, finally mixing the iron phthalocyanine/modified active carbon and sulfur powder, then placing the mixture in an inert atmosphere for heat treatment, pyrolyzing the iron phthalocyanine/modified active carbon to form nitrogen-doped carbon/modified active carbon, and simultaneously reacting a byproduct molybdenum trioxide generated in the process of synthesizing the iron phthalocyanine/modified active carbon with gaseous sulfur at high temperature to grow molybdenum disulfide in situ to obtain MoS2The nitrogen-doped carbon/modified activated carbon sodium ion battery negative electrode material. The method has the characteristics of simple process, good repeatability, high safety and the like, the prepared material has a high specific surface area, and the stability of sodium storage is improved by using the phthalocyanine iron cracking nitrogen-doped carbon as a molybdenum disulfide/modified activated carbon interface.

Description

MoS2Nitrogen-doped carbon/modified activated carbon sodium ion battery negative electrode material and preparation method thereof
Technical Field
The invention relates to the technical field of sodium ion batteries, in particular to a MoS2A nitrogen-doped carbon/modified activated carbon sodium ion battery cathode material and a preparation method thereof.
Background
The problem of environmental pollution is increasingly prominent, clean energy sources such as wind energy and solar energy are more and more concerned by people, but the energy sources are intermittent and limit the development and wide application of the clean energy sources, and a large-scale energy storage technology is a key technology for solving the bottleneck of efficient utilization of renewable energy sources. The lithium ion battery is an important energy storage technology, is widely applied to portable electronic equipment and new energy automobiles, and is restricted by lithium resource shortage and high price in large-scale development along with the development of electric automobiles and smart power grids. Sodium and lithium have the same main group, similar electronic configuration and chemical properties, abundant sodium reserves and low price, so that the sodium-ion battery is considered as a secondary rechargeable battery which is most easy to replace a lithium-ion battery. The distance between graphite layers is 0.335nm, and the theoretical specific capacity of the graphite layer when the graphite layer is used as the cathode of a lithium ion battery is 372mAh g-1However, sodium graphite intercalation compounds are difficult to form, with only a small amount of Na+Can store upIn the presence of graphite, the reversible capacity is therefore low (. apprxeq.35 mAh g)-1) And the requirements of the sodium ion battery cannot be met.
Molybdenum disulfide (MoS)2) Is a two-dimensional layered compound with a structure similar to graphite, atoms in the S-Mo-S layer are strongly bonded by covalent bonds, and S-Mo-S layers are bonded by Van der Waals force, the interlayer spacing is up to 0.62nm, is 1.85 times of the graphite interlayer spacing (0.335nm), is favorable for repeated intercalation/deintercalation of sodium ions with larger radius, and the theoretical specific capacity reaches 670mAh g-1Is one of the most potential sodium ion battery cathode materials. However, MoS2The lamella is easy to stack in the charging and discharging process, active sites are necrotic, the circulation stability and the rate capability are poor, and MoS2Poor conductivity limits its application.
Disclosure of Invention
In order to solve the problems in the prior art, the invention provides a MoS2The preparation method has the advantages of simple process, short period, high repeatability, lower cost, environmental protection and safety, is beneficial to large-scale production, and the prepared MoS2the/NC/FAC nano composite material has a stable structure and has excellent cycling stability when being used as a negative electrode material of a sodium-ion battery.
To achieve the above object, the present invention provides a MoS2The preparation method of the/nitrogen-doped carbon/modified activated carbon sodium ion battery negative electrode material comprises the following steps:
1) transferring the activated carbon into a nitric acid solution by adopting a water bath heating method, stirring, heating at 50-100 ℃, and keeping the temperature for 6-30 hours to obtain modified activated carbon;
2) an in-situ solid phase method is adopted, 0.41-1.71 g of phthalic anhydride, 1.02-2.56 g of urea, 0.16-2.48 g of ammonium molybdate and 0.69-2.02 g of ferrous ammonium sulfate hexahydrate are used as raw materials, 0.06-0.41 g of modified activated carbon is used as a substrate, sintering is carried out at 270 ℃, and heat preservation is carried out for 2 hours, so as to synthesize iron phthalocyanine/modified activated carbon;
3) keeping the equal mass of iron phthalocyanine/modified activated carbon and sulfur powder at 800-1000 ℃ in inert atmosphere for 1-E2 hours, cracking the mixture at high temperature into nitrogen-doped carbon and growing molybdenum disulfide in situ to obtain MoS2The nitrogen-doped carbon/modified activated carbon sodium ion battery negative electrode material.
Preferably, the concentration of the nitric acid solution in the step 1) is 1-5 mol/L.
Preferably, after the heat preservation in the step 1) is finished, the product is washed, filtered and dried by water.
Preferably, in the step 2), phthalic anhydride, urea, ammonium molybdate, ammonium ferrous sulfate hexahydrate and modified activated carbon are mixed, ground uniformly and then sintered in a muffle furnace.
Preferably, the sintering in step 2) is performed at 10 ℃ for min-1The temperature rising rate is increased from room temperature to 270 ℃, the temperature is kept for 2h, the product is naturally cooled to room temperature after the temperature keeping is finished, and the product is purified by ultrapure water and then dried to obtain the iron phthalocyanine/modified activated carbon.
Preferably, in the step 3), the iron phthalocyanine/modified activated carbon and the sulfur powder are mixed and ground uniformly and then placed in a tubular furnace for reaction.
Preferably, the reaction in the step 3) is carried out under an argon atmosphere, and the flow rate of argon is 10-50 sccm.
Preferably, the tubular furnace in the step 3) is used for 10 ℃ min-1The temperature rising rate is increased from room temperature, the reaction product is naturally cooled to room temperature after the reaction is finished, the product is purified and dried, the purification is that the product is respectively washed for a plurality of times by using ultrapure water and absolute ethyl alcohol, and the drying is that the product is dried in vacuum for 12-36 hours.
The invention also provides a MoS2The nitrogen-doped carbon/modified activated carbon sodium ion battery cathode material adopts the MoS2The preparation method of the/N-doped carbon/modified activated carbon sodium ion battery cathode material comprises the steps of taking the modified activated carbon as a substrate, taking the N-doped carbon as a transition layer, and preparing MoS2The nanosheets are uniformly grown on the substrate and the transition layer at 0.5A g-1The initial discharge capacity was 831.5mAh g when cycled at a current density of (1)-1The first coulombic efficiency was 67.3%, and after 100 cycles, the capacity remained 353.1mAh g-1。
Compared with the prior art, the preparation method of the inventionFirstly, performing water-bath heat treatment on activated carbon by using a nitric acid solution to modify the activated carbon to obtain modified activated carbon (FAC) with surfaces rich in active functional groups; then, the iron phthalocyanine/modified activated carbon (FePc/FAC) is prepared in one step by an in-situ solid phase method, and finally, the iron phthalocyanine/modified activated carbon and sulfur powder are fully mixed and then subjected to heat treatment, so that on one hand, the iron phthalocyanine/modified activated carbon is cracked into nitrogen-doped carbon, and on the other hand, molybdenum disulfide grows in situ by utilizing the action of a byproduct molybdenum trioxide generated in the process of synthesizing the iron phthalocyanine/modified activated carbon and gaseous sulfur at high temperature, and the MoS is obtained2The nitrogen-doped carbon/modified activated carbon sodium ion battery negative electrode material. MoS2The carbon material is compounded with the carbon material, so that the conductivity can be improved, the volume change in the charging and discharging process is relieved, the stability of the electrode structure is improved, the activated carbon is not easy to adhere, and the carbon material has the advantages of high specific surface area, simple production process, low cost and the like. Wherein, nitric acid modifies the activated carbon to increase the surface active functional groups, which is favorable for MoS2Provides nucleation sites and can also significantly inhibit MoS2Stacking the sheets; reconstructing a transition layer to further stabilize the structure and improving MoS by regulating and controlling the chemical structure and microstructure2The stability and the conductivity of/NC/FAC are realized by adopting nitric acid modified activated carbon (FAC) as a conductive substrate, and the nitric acid modification treatment is favorable for increasing oxygen-containing functional groups on the surface of the FAC so as to increase MoS2The interface bonding strength of (2), stability and conductivity are improved. In addition, on the basis of nitric acid modified activated carbon, a carbon transition layer doped with iron phthalocyanine cracking nitrogen is introduced to further regulate and control a molybdenum disulfide/modified activated carbon interface. Through the synergistic effect among three components in the composite structure system, the stability is improved, and the conductivity is improved, so that the high-performance sodium storage is realized. The preparation process is simple and easy to control, low in energy consumption and good in repeatability, and is beneficial to industrial production.
MoS prepared by the invention2N-doped carbon/modified activated carbon sodium ion battery negative electrode material (MoS)2/NC/FAC)，MoS2The nano-sheet grows uniformly on a material with FAC as a substrate and NC as a transition layer, the size distribution is uniform, the size distribution is about 100nm, and MoS2The ternary composite material of/NC/FAC is 0.5A g-1When circulating at a current density of (2), it is initiallyThe discharge capacity is 831.5mAh g-1The first coulombic efficiency was 67.3%, and after 100 cycles, the capacity remained 353.1mAh g-1. The results show that MoS2The sodium storage stability of/NC/FAC is higher than that of MoS2a/FAC electrode material. The ternary system MoS2The negative electrode material of the/NC/FAC sodium-ion battery shows excellent conductivity, cycling stability and high specific discharge capacity, and can be widely used as the negative electrode material of the sodium-ion battery.
Drawings
FIG. 1 shows MoS obtained in example 32XRD pattern of/NC/FAC sodium ion battery cathode material;
FIG. 2 shows MoS obtained in example 32SEM image of/NC/FAC sodium ion battery cathode material;
FIG. 3 shows MoS obtained in example 32Negative electrode material of/NC/FAC sodium ion battery and MoS prepared by comparative example2Comparative chart of cycle performance test of negative electrode material of FAC sodium ion battery.
Detailed Description
The present invention will be further explained with reference to the drawings and specific examples in the specification, and it should be understood that the examples described are only a part of the examples of the present application, and not all examples. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present application.
The invention discloses a MoS2The preparation method of the/nitrogen-doped carbon/modified activated carbon sodium ion battery negative electrode material specifically comprises the following steps:
1) transferring the activated carbon into a nitric acid solution with the concentration of 1-5 mol/L by adopting a water bath heating method, stirring, heating and insulating for 6-30 hours at 50-100 ℃, and washing, filtering, and drying a product after the insulation to obtain modified activated carbon;
2) by adopting an in-situ solid phase method, 0.41-1.71 g of phthalic anhydride, 1.02-2.56 g of urea, 0.16-2.48 g of ammonium molybdate and 0.69-2.02 g of ferrous ammonium sulfate hexahydrate are used as raw materials, 0.06-0.41 g of modified activated carbon is used as a substrate, the raw materials are mixed and ground uniformly, and then the mixture is subjected to in-situ solid phase methodSintering the mixture in a muffle furnace at 270 ℃ and preserving heat for 2 hours to synthesize iron phthalocyanine/modified activated carbon; preferably, the sintering is performed at 10 ℃ for min-1The temperature rising rate is increased from room temperature to 270 ℃, the temperature is preserved for 2 hours, the temperature is naturally cooled to room temperature after the temperature preservation is finished, and the product is purified by ultrapure water and then dried;
3) uniformly mixing and grinding the iron phthalocyanine/modified activated carbon and the sulfur powder with equal mass, placing the mixture in a tube furnace, preserving the heat for 1-2 hours at 800-1000 ℃ under inert atmosphere, cracking the mixture at high temperature to form nitrogen-doped carbon, and growing molybdenum disulfide in situ to obtain MoS2and/NC/FAC. Preferably, the reaction is carried out in an argon atmosphere at an argon flow rate of 10-50 sccm and in a tube furnace at 10 ℃ for min-1The temperature rising rate is increased from room temperature, the reaction product is naturally cooled to room temperature after the reaction is finished, the product is purified and dried, the purification is that the product is respectively washed for a plurality of times by using ultrapure water and absolute ethyl alcohol, and the drying is that the product is dried in vacuum for 12-36 hours.
The invention also provides a MoS2The nitrogen-doped carbon/modified activated carbon sodium ion battery cathode material is prepared by the preparation method, namely MoS2the/NC/FAC takes modified active carbon as a substrate, nitrogen-doped carbon as a transition layer and MoS2The nanosheets are uniformly grown on the substrate and the transition layer at 0.5A g-1The initial discharge capacity was 831.5mAh g when cycled at a current density of (1)-1The first coulombic efficiency was 67.3%, and after 100 cycles, the capacity remained 353.1mAh g-1。
The present invention will be described in detail with reference to specific examples.
Example 1:
the method comprises the following steps:
1) adding activated carbon into a nitric acid solution with the concentration of 1mol/L, heating to 100 ℃ while magnetically stirring, preserving heat for 6 hours, washing, filtering, and drying after the heat preservation is finished to obtain nitric acid modified activated carbon (FAC);
2) weighing 0.41g of phthalic anhydride, 1.02g of urea, 0.16g of ammonium molybdate, 0.69g of ammonium ferrous sulfate hexahydrate and 0.06g of FAC, grinding uniformly in a glass mortar, and placing in a muffle furnace at 10 ℃ for min-1The temperature rising rate is increased from room temperature to 270 ℃, the temperature is kept for 2 hours, and after the temperature keeping is finishedNaturally cooling to room temperature, purifying with ultrapure water, and drying to obtain FePc/FAC;
3) 0.38g of FePc/FAC and 0.38g of sulfur powder are mixed and ground uniformly, and the mixture is transferred into a tube furnace in the argon atmosphere and is heated for 10 min-1The temperature rising rate is increased from room temperature to 1000 ℃, the temperature is kept for 1h, and the mixture is naturally cooled;
4) collecting the above products, washing with deionized water and anhydrous ethanol for 3 times respectively, and vacuum drying for 36h to obtain MoS2The negative electrode material of the/NC/FAC sodium-ion battery.
Example 2:
the method comprises the following steps:
1) adding activated carbon into a nitric acid solution with the concentration of 2mol/L, heating to 60 ℃ while magnetically stirring, preserving heat for 12 hours, washing, filtering and drying after the heat preservation is finished to obtain nitric acid modified activated carbon (FAC);
2) weighing 0.73g of phthalic anhydride, 1.42g of urea, 0.31g of ammonium molybdate, 1.05g of ammonium ferrous sulfate hexahydrate and 0.13g of FAC, grinding uniformly in a glass mortar, and placing in a muffle furnace at 10 ℃ for min-1Raising the temperature from room temperature to 270 ℃ at the temperature raising rate, preserving the heat for 2 hours, naturally cooling to room temperature after the heat preservation is finished, purifying with ultrapure water, and drying to obtain FePc/FAC;
3) 0.38g of FePc/FAC and 0.38g of sulfur powder are mixed and ground uniformly, and the mixture is transferred into a tube furnace in the argon atmosphere and is heated for 10 min-1The temperature rising rate is increased from room temperature to 950 ℃, the temperature is kept for 1h, and the mixture is naturally cooled;
4) collecting the above products, washing with deionized water and anhydrous ethanol for 3 times respectively, and vacuum drying for 24h to obtain MoS2The negative electrode material of the/NC/FAC sodium-ion battery.
Example 3:
the method comprises the following steps:
1) adding activated carbon into a nitric acid solution with the concentration of 3mol/L, heating to 80 ℃ while magnetically stirring, preserving heat for 18 hours, washing, filtering and drying after the heat preservation is finished to obtain nitric acid modified activated carbon (FAC);
2) 1.05g of phthalic anhydride, 1.81g of urea, 0.62g of ammonium molybdate, 1.38g of ammonium ferrous sulfate hexahydrate and 0.23g of FAC are weighed and ground in a glass mortarAfter being homogenized, the mixture is placed in a muffle furnace for 10 ℃ min-1Raising the temperature from room temperature to 270 ℃ at the temperature raising rate, preserving the heat for 2 hours, naturally cooling to room temperature after the heat preservation is finished, purifying with ultrapure water, and drying to obtain FePc/FAC;
3) 0.38g of FePc/FAC and 0.38g of sulfur powder are mixed and ground uniformly, and the mixture is transferred into a tube furnace in the argon atmosphere and is heated for 10 min-1The temperature rising rate is increased from room temperature to 900 ℃, the temperature is kept for 2h, and the product is naturally cooled;
4) collecting the above products, washing with deionized water and anhydrous ethanol for 3 times respectively, and vacuum drying for 12h to obtain MoS2The negative electrode material of the/NC/FAC sodium-ion battery.
Referring to FIG. 1, it can be seen from FIG. 1 that the product produced is MoS2Comparing with standard PDF card, the NC/FAC shows that the peak position of the diffraction peak is basically completely matched, which indicates that the prepared product is the target product MoS2/NC/FAC。
See FIG. 2, by MoS2MoS can be found in a topographic map of/NC/FAC2The nano-sheet grows uniformly on a material which takes FAC as a substrate and NC as a transition layer, and the size distribution is uniform and about 100 nm.
For comparison, design MOS2Comparative example prepared by FAC: mixing ammonium molybdate 1.05g, sulfur powder 2.03g and modified active carbon 0.12g, grinding uniformly, transferring into a tube furnace at 10 deg.C for 10 min-1The heating rate is increased from room temperature to 750 ℃, the temperature is kept for 2h, the mixture is naturally cooled to room temperature, and the mixture is washed for 3 times by deionized water and absolute ethyl alcohol and then is dried for 12h in vacuum, so that MoS is obtained2A negative electrode material of FAC sodium ion battery.
Referring to FIG. 3, MoS can be seen from FIG. 32When the/NC/FAC nano composite material is used as the cathode material of the sodium-ion battery, compared with the M prepared by the comparative exampleOS2/FAC with significant capacity increase and improved cycling stability, MoS2(NC/FAC at 0.5A g-1The initial discharge capacity of 831.5mAh g when cycled at a current density of-1The first coulombic efficiency was 67.3%, and after 100 cycles, the capacity remained 353.1mAh g-1. The results show that MoS2Sodium storage stability of/NC/FACQualitative higher than MoS2a/FAC electrode material.
Example 4:
the method comprises the following steps:
1) adding activated carbon into a nitric acid solution with the concentration of 4mol/L, heating to 50 ℃ while magnetically stirring, preserving heat for 24 hours, washing, filtering and drying after the heat preservation is finished to obtain nitric acid modified activated carbon (FAC);
2) weighing 1.37g of phthalic anhydride, 2.21g of urea, 1.24g of ammonium molybdate, 1.71g of ammonium ferrous sulfate hexahydrate and 0.32g of FAC, grinding uniformly in a glass mortar, and placing in a muffle furnace at 10 ℃ for min-1Raising the temperature from room temperature to 270 ℃ at the temperature raising rate, preserving the heat for 2 hours, naturally cooling to room temperature after the heat preservation is finished, purifying with ultrapure water, and drying to obtain FePc/FAC;
3) 0.38g of FePc/FAC and 0.38g of sulfur powder are mixed and ground uniformly, and the mixture is transferred into a tube furnace in the argon atmosphere and is heated for 10 min-1The temperature rising rate is increased from room temperature to 900 ℃, the temperature is kept for 2h, and the product is naturally cooled;
4) collecting the above products, washing with deionized water and anhydrous ethanol for 3 times respectively, and vacuum drying for 20h to obtain MoS2The negative electrode material of the/NC/FAC sodium-ion battery.
Example 5:
the method comprises the following steps:
1) adding activated carbon into a nitric acid solution with the concentration of 5mol/L, heating to 70 ℃ while magnetically stirring, preserving heat for 30 hours, washing, filtering, and drying after the heat preservation is finished to obtain nitric acid modified activated carbon (FAC);
2) weighing 1.71g of phthalic anhydride, 2.56g of urea, 2.48g of ammonium molybdate, 2.02g of ammonium ferrous sulfate hexahydrate and 0.41g of FAC, grinding uniformly in a glass mortar, and placing in a muffle furnace at 10 ℃ for min-1Raising the temperature from room temperature to 270 ℃ at the temperature raising rate, preserving the heat for 2 hours, naturally cooling to room temperature after the heat preservation is finished, purifying with ultrapure water, and drying to obtain FePc/FAC;
3) 0.38g of FePc/FAC and 0.38g of sulfur powder are mixed and ground uniformly, and the mixture is transferred into a tube furnace in the argon atmosphere and is heated for 10 min-1The temperature rising rate is increased from room temperature to 800 ℃, the temperature is kept for 1h, and the mixture is naturally cooled;
4) collecting the above products, washing with deionized water and anhydrous ethanol for 3 times respectively, and vacuum drying for 30h to obtain MoS2The negative electrode material of the/NC/FAC sodium-ion battery.
The preparation method comprises the steps of firstly modifying the activated carbon by adopting a nitric acid solution water-bath heat treatment method to obtain modified activated carbon (FAC), then synthesizing iron phthalocyanine/FAC (FePc/FAC) by adopting an in-situ solid-phase method, finally uniformly mixing the FePc/FAC and sulfur powder, then placing the mixture in an argon atmosphere, cracking the FePc/FAC into nitrogen-doped carbon/FAC at high temperature, and simultaneously utilizing the action of molybdenum trioxide and sulfur powder which are byproducts of FePc synthesis to grow MoS in situ2Obtaining MoS2The method has novel design thought, and the MoS is prepared by adopting a high-temperature heat treatment process2a/NC/FAC nanocomposite material, thereby avoiding MOS2The cyclic stability of the material is improved. The method adopted by the invention has the characteristics of simple process, good repeatability, high safety and the like. MoS prepared by the invention2The/nitrogen-doped carbon/modified activated carbon ternary nano composite material has a high specific surface area, and can be used as an excellent sodium ion battery cathode material by using the phthalocyanine iron cracking nitrogen-doped carbon as a molybdenum disulfide/modified activated carbon interface to improve the sodium storage stability.
Finally, it should be noted that: the above embodiments are only used to illustrate the technical solution of the present invention, and not to limit the same; although the present invention has been described in detail with reference to the foregoing embodiments, it will be understood by those of ordinary skill in the art that: the technical solutions described in the foregoing embodiments may still be modified, or some or all of the technical features may be equivalently replaced; and the modifications or the substitutions do not make the essence of the corresponding technical solutions depart from the scope of the technical solutions of the embodiments of the present invention.

Claims (9)

1. MoS2The preparation method of the/nitrogen-doped carbon/modified activated carbon sodium ion battery negative electrode material is characterized by comprising the following steps of:
1) transferring the activated carbon into a nitric acid solution by adopting a water bath heating method, stirring, heating at 50-100 ℃, and keeping the temperature for 6-30 hours to obtain modified activated carbon;
2) an in-situ solid phase method is adopted, 0.41-1.71 g of phthalic anhydride, 1.02-2.56 g of urea, 0.16-2.48 g of ammonium molybdate and 0.69-2.02 g of ferrous ammonium sulfate hexahydrate are used as raw materials, 0.06-0.41 g of modified activated carbon is used as a substrate, sintering is carried out at 270 ℃, and heat preservation is carried out for 2 hours, so as to synthesize iron phthalocyanine/modified activated carbon;
3) keeping the same mass of iron phthalocyanine/modified activated carbon and sulfur powder at 800-1000 ℃ for 1-2 hours in an inert atmosphere, pyrolyzing the iron phthalocyanine/modified activated carbon and sulfur powder to form nitrogen-doped carbon, and growing molybdenum disulfide in situ to obtain MoS2The nitrogen-doped carbon/modified activated carbon sodium ion battery negative electrode material.
2. A MoS according to claim 12The preparation method of the/nitrogen-doped carbon/modified activated carbon sodium ion battery negative electrode material is characterized in that the concentration of a nitric acid solution in the step 1) is 1-5 mol/L.
3. A MoS according to claim 12The preparation method of the/nitrogen-doped carbon/modified activated carbon sodium ion battery cathode material is characterized in that a product is washed, filtered and dried by water after the heat preservation in the step 1) is finished.
4. A MoS according to claim 12The preparation method of the/nitrogen-doped carbon/modified activated carbon sodium ion battery cathode material is characterized in that phthalic anhydride, urea, ammonium molybdate, ammonium ferrous sulfate hexahydrate and modified activated carbon in the step 2) are mixed, ground uniformly and then sintered in a muffle furnace.
5. A MoS according to claim 42The preparation method of the/N-doped carbon/modified activated carbon sodium ion battery cathode material is characterized in that the sintering in the step 2) is carried out for 10 min-1Heating up to 270 ℃ from room temperature at the heating rate, keeping the temperature for 2h, naturally cooling to room temperature after the heat preservation is finished, purifying the product with ultrapure water, and drying to obtain the iron phthalocyanineModified activated carbon.
6. A MoS according to claim 12The preparation method of the/N-doped carbon/modified activated carbon sodium ion battery cathode material is characterized in that in the step 3), the iron phthalocyanine/modified activated carbon and the sulfur powder are mixed, ground uniformly and then placed in a tubular furnace for reaction.
7. A MoS according to claim 62The preparation method of the/nitrogen-doped carbon/modified activated carbon sodium ion battery negative electrode material is characterized in that the reaction in the step 3) is carried out in an argon atmosphere, and the flow rate of argon is 10-50 sccm.
8. A MoS according to claim 62The preparation method of the/N-doped carbon/modified activated carbon sodium ion battery cathode material is characterized in that the tubular furnace in the step 3) is used for 10 ℃ min-1The temperature rising rate is increased from room temperature, the reaction product is naturally cooled to room temperature after the reaction is finished, the product is purified and dried, the purification is that the product is respectively washed for a plurality of times by using ultrapure water and absolute ethyl alcohol, and the drying is that the product is dried in vacuum for 12-36 hours.
9. MoS2A/N-doped carbon/modified activated carbon sodium ion battery negative electrode material, characterized in that the MoS of any one of claims 1 to 8 is adopted2The preparation method of the/N-doped carbon/modified activated carbon sodium ion battery cathode material comprises the steps of taking the modified activated carbon as a substrate, taking the N-doped carbon as a transition layer, and preparing MoS2The nanosheets are uniformly grown on the substrate and the transition layer at 0.5A g-1The initial discharge capacity was 831.5mAh g when cycled at a current density of (1)-1The first coulombic efficiency was 67.3%, and after 100 cycles, the capacity remained 353.1mAh g-1。
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114597400A (en) * 2022-03-02 2022-06-07 陕西科技大学 MoS2Acetylene black flexible sulfur fixation material, preparation method thereof, sulfur fixation method and lithium-sulfur battery positive electrode

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108923050A (en) * 2018-07-04 2018-11-30 武汉大学 A kind of carbon nano-structured elctro-catalyst of the nucleocapsid of high catalytic performance and preparation method thereof
CN109065867A (en) * 2018-08-03 2018-12-21 西北工业大学 Molybdenum disulfide/nitrogen-doped carbon nano wire negative electrode material preparation method
CN111063889A (en) * 2019-12-20 2020-04-24 陕西科技大学 Iron phthalocyanine/active carbon Li/SOCl2Preparation method of battery anode catalytic material
CN111276679A (en) * 2020-01-22 2020-06-12 天津大学 Double-carbon composite molybdenum sulfide composite material for sodium ion battery cathode material and preparation method thereof
CN112928260A (en) * 2021-02-23 2021-06-08 多助科技(武汉)有限公司 Molybdenum disulfide/iron sulfide/nitrogen-doped carbon composite material and preparation and application thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108923050A (en) * 2018-07-04 2018-11-30 武汉大学 A kind of carbon nano-structured elctro-catalyst of the nucleocapsid of high catalytic performance and preparation method thereof
CN109065867A (en) * 2018-08-03 2018-12-21 西北工业大学 Molybdenum disulfide/nitrogen-doped carbon nano wire negative electrode material preparation method
CN111063889A (en) * 2019-12-20 2020-04-24 陕西科技大学 Iron phthalocyanine/active carbon Li/SOCl2Preparation method of battery anode catalytic material
CN111276679A (en) * 2020-01-22 2020-06-12 天津大学 Double-carbon composite molybdenum sulfide composite material for sodium ion battery cathode material and preparation method thereof
CN112928260A (en) * 2021-02-23 2021-06-08 多助科技(武汉)有限公司 Molybdenum disulfide/iron sulfide/nitrogen-doped carbon composite material and preparation and application thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
刘鑫悦: "活性炭支撑纳米MoS2的制备及储钠性能研究", 《中国优秀博硕士学位论文全文数据库（硕士） 工程科技I辑》 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114597400A (en) * 2022-03-02 2022-06-07 陕西科技大学 MoS2Acetylene black flexible sulfur fixation material, preparation method thereof, sulfur fixation method and lithium-sulfur battery positive electrode

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