Disclosure of Invention
In order to solve the problems of complex equipment, complex process, complex and time-consuming operation, low product utilization rate, difficult raw material acquisition, low nitrogen doping content caused by the loss of a large amount of nitrogen-doped precursors in the nitrogen doping process and the like in the preparation of the nitrogen-doped graphene material in the prior art, the invention provides a method for efficiently, quickly and massively synthesizing the high-nitrogen-content doped graphene material.
In order to achieve the above technical object, a first aspect of the present invention provides a method for preparing a nitrogen-doped graphene material, including the following steps:
(1) Dispersing graphene oxide in a formaldehyde aqueous solution to obtain a dispersion liquid A;
(2) Dispersing melamine into deionized water to obtain a dispersion liquid B;
(3) Mixing the dispersion liquid A and the dispersion liquid B, heating to 50-80 ℃, reacting for 10-60min, adjusting the pH of the reaction liquid to 7-9, heating to 100-200 ℃ in a sealed manner, carrying out hydrothermal reaction for 5-30 h, filtering, and drying to obtain black solid powder;
(4) And (4) placing the black solid powder obtained in the step (3) in a microwave reaction chamber, and heating for 1-60min at the microwave power of 300-1200W to obtain the nitrogen-doped graphene material.
In the above-mentioned production method, the concentration of the aqueous formaldehyde solution in the step (1) is not particularly limited, and in a preferred embodiment of the present invention, the concentration of formaldehyde is 37% to 40% by mass. And mixing the graphene oxide with formaldehyde solution according to the solid-to-liquid ratio of 1g (10-100) mL. Preferably, the mixture is uniformly mixed and dispersed in an ultrasonic mode, and the ultrasonic time is 5-30min.
In the above production method, the dispersion liquid a and the dispersion liquid B are mixed in the step (3), and the dispersion liquid a is preferably poured into the dispersion liquid B. Mixing the graphene in the dispersion liquid A and the melamine in the dispersion liquid B in a ratio of 1-20 by mass. After mixing, the mixture is preferably mixed and dispersed uniformly in an ultrasonic mode, and the ultrasonic time is 5-30min.
In the above preparation method, the pH of the reaction solution in the step (3) may be adjusted by using an organic base or an inorganic base, and as a more specific embodiment, the pH is selected from one or more of methylamine, ethylamine, ethylenediamine, propylamine, isopropylamine, triethanolamine, aniline, cyclohexylamine, o-aminophenol, 2-chlorophenol, potassium carbonate, sodium bicarbonate, potassium hydroxide, and sodium hydroxide.
In the preparation method, the hydrothermal reaction temperature in the step (3) is preferably 120 to 160 ℃, and the time is preferably 12 to 18h.
In the preparation method, the power of the microwave reaction in the step (4) is preferably 600 to 1000W, and the time is preferably 10 to 30min.
In the preparation method, the microwave reaction cavity is purged by nitrogen or inert gas before and during the microwave reaction, and preferably, argon is used for purging.
In the above preparation method, the graphene oxide is selected from among graphene oxides having the following properties: the area of the sheet layer is 100 mu m 2 The conductivity is 3500S/m or more.
In the above preparation method, the graphene oxide is obtained by oxidizing graphite, and the graphene oxide of the present invention is synthesized by Hummers method, and as a more specific embodiment, the present invention discloses a specific preparation method of the graphite oxide as follows: adding natural crystalline flake graphite into ice-bath concentrated sulfuric acid under the condition of stirring, cooling to 0-10 ℃, adding sodium nitrate and potassium permanganate, stirring for reaction, adding deionized water, heating to 50-100 ℃, reacting at constant temperature until the reaction solution turns bright yellow, adding hydrogen peroxide, stirring for reaction, cooling, washing and drying to obtain the graphene oxide.
The specification of the natural crystalline flake graphite is 100-500 meshes. After the reaction is finished, repeatedly settling with deionized water during post-treatment to remove unreacted graphite particles, centrifuging with hydrochloric acid, cleaning, removing Cl ions in the reaction solution, washing with deionized water until the pH value is close to neutral, drying, and grinding.
The stripping efficiency of the Hummers method is more than 93%, the yield is more than 90%, the structural integrity of the obtained graphene oxide sheet layer is high, and the crystal lattice is complete after thermal reduction.
The technical purpose of the second aspect of the invention is to provide the nitrogen-doped graphene material prepared by the method. In the preparation process of the method, formaldehyde and melamine are mixed firstly to generate moderate crosslinking reaction to form a water-soluble nitrogen-doped precursor, and then hydrothermal reaction is carried out to carry out graphene nitrogen doping, so that the nitrogen-doped precursor and graphene components are easy to interact, conditions are created for uniformly fusing composite materials, and the nitrogen-doped process is more favorably realized; subsequent microwave reaction heating rate is fast, the heating is even, and graphite oxide is reduced into graphite alkene by heat rapidly, and the nitrogen-doped precursor is heated and is decomposed simultaneously, because graphite oxide and nitrogen-doped precursor evenly fuse together in the preparation process before, make graphite alkene nitrogen doping more even, are favorable to synthesizing high content nitrogen doping graphite alkene more.
The technical purpose of the third aspect of the invention is to provide application of the nitrogen-doped graphene material, and the material can be used as a lithium ion battery cathode material and shows good cycle stability and rate capability.
Compared with the prior art, the invention has the following advantages:
(1) According to the preparation method, formaldehyde is used as a bridge in the preparation process of the nitrogen-doped graphene material, and the formaldehyde and melamine are appropriately crosslinked to form the nitrogen-doped precursor, so that the problem of low nitrogen-doping efficiency caused by large loss of the nitrogen-doped precursor due to strong sublimation of the nitrogen-doped precursor in the heating process in the traditional solid nitrogen-doping reaction is solved.
(2) In the preparation process, the formaldehyde and the melamine are subjected to a cross-linking reaction to form a water-soluble nitrogen-doped precursor, so that the nitrogen-doped precursor and the graphene are uniformly fused through interaction in the subsequent hydrothermal reaction, and the preparation of the high-nitrogen-content doped graphene material is realized.
(3) Above-mentioned microwave reaction stage in the preparation process, the rate of heating is fast, the heating is even, can avoid the loss that the sublimation of the nitrogen-doped precursor that slowly heaies up in traditional reaction caused on the one hand, on the other hand, under the microwave condition, graphite oxide is rapidly by thermal reduction for graphite alkene, nitrogen-doped precursor is heated simultaneously and decomposes, because graphite oxide and nitrogen-doped precursor evenly fuse together in hydrothermal reaction process before, make graphite alkene nitrogen doping more even, more be favorable to synthesizing high nitrogen content doping graphite alkene, effectively alleviate long-time heat treatment in-process nanoparticle's gathering and piling up.
(4) The microwave reaction in the preparation process adopts a solvent-free treatment mode, so that the post-treatment processes of washing, separating, drying and the like of the product are omitted, and the production process is simplified.
(5) The nitrogen-doped graphene material prepared by the method has good stability, is not easy to denature in air, is easy to store, has a large specific surface area, is used as a lithium ion battery cathode material, provides a good channel for lithium ion transmission, and shows a large specific capacity and a good cycling stability performance.
Additional features and advantages of the invention will be set forth in the detailed description which follows.
Detailed Description
The following non-limiting examples are presented to enable those of ordinary skill in the art to more fully understand the present invention and are not intended to limit the invention in any way.
The graphene oxide used in the following examples was prepared by the following method:
100mL of 98% concentrated sulfuric acid was slowly added to 500mL of a dry three-necked flask, and the three-necked flask was placed on a magnetic stirrer with ice-bath cooling. 2.0g of natural crystalline flake graphite (180 mesh) was added with rapid stirring, and when the temperature of the reaction solution was reduced to about 0 ℃, 4.0g of sodium nitrate was slowly added, and stirring was continued for 2 hours. Then slowly adding 10g of potassium permanganate in batches within 1h, continuously stirring for 2h, and controlling the reaction temperature below 10 ℃. The three-necked flask is transferred into a water bath at 40 ℃, and the reaction is continuously stirred for 2 hours. Subsequently, 200mL of warm deionized water was added slowly and the reaction solution was kept at a temperature within 100 ℃. The reaction was carried out at a constant temperature of 98 ℃ until the reaction solution became bright yellow. Adding 20mL of 30% hydrogen peroxide into the reaction solution, and continuously stirringStirring to make it fully react. And after cooling, replacing deionized water with the obtained solution for repeated sedimentation, removing unreacted graphite particles, centrifugally cleaning with hydrochloric acid to remove Cl ions in the reaction solution, and then washing with deionized water until the pH value is close to neutral. And finally, vacuum drying for 12h at 80 ℃ to obtain graphene oxide, and grinding the graphene oxide into powder for later use. Its XRD pattern is shown in FIG. 1 and is located at 11 o To the left and right is the typical 001 diffraction peak of graphene oxide, which is mainly due to the intercalation of a large number of oxygen-containing functional groups between graphene sheets. The distance between graphite oxide sheets can be calculated to be 0.7 nm by the Sheer formula, and is obviously larger than the interlayer spacing of graphite by 0.3254 nm. The increased interlayer spacing is primarily due to oxygen-containing functional groups intercalated between graphene sheets.
Nitrogen-doped graphene materials of the present invention were prepared in examples 1 to 8:
example 1
(1) 1.0g of graphene oxide was weighed and dispersed in 20mL of 37% formaldehyde aqueous solution, and the dispersion was uniformly dispersed in an ultrasonic instrument and recorded as dispersion A.
(2) 3.0g of melamine is weighed and added into 40mL of deionized water, and the mixture is placed in an ultrasonic instrument to be uniformly dispersed by ultrasonic, and the dispersion liquid B is marked.
(3) Mixing the dispersion A and the dispersion B, heating in water bath to 60 ℃, and stirring for 10min. And adding triethanolamine into the reaction solution, adjusting the pH value of a reaction solution system to 8.0, ultrasonically mixing uniformly, pouring the reaction solution into a high-pressure reaction kettle, and heating to 120 ℃ for reaction for 12 hours. And (4) carrying out suction filtration and vacuum drying to obtain black solid powder.
(4) And (4) placing the black solid powder obtained in the step (3) in a microwave reaction chamber, and purging for 1h by 100mL/min argon. And heating for 10min at the microwave power of 600W to obtain the nitrogen-doped graphene material.
Example 2
(1) 1.0g of graphene oxide was weighed and dispersed in 30mL of 37% aqueous formaldehyde solution, and the dispersion was uniformly dispersed in an ultrasonic instrument and recorded as dispersion A.
(2) 5.0g of melamine is weighed and added into 40mL of deionized water, and the mixture is placed in an ultrasonic instrument and is uniformly dispersed by ultrasound to be marked as dispersion B.
(3) Mixing the dispersion A and the dispersion B, heating to 60 ℃ in a water bath, and stirring for 10min. And adding triethanolamine into the reaction solution, adjusting the pH value of a reaction solution system to 8.0, uniformly mixing by ultrasonic waves, pouring the reaction solution into a high-pressure reaction kettle, and heating to 120 ℃ for reaction for 12 hours. And (4) carrying out suction filtration and vacuum drying to obtain black solid powder.
(4) And (4) placing the black solid powder obtained in the step (3) in a microwave reaction chamber, and purging with 100mL/min of argon for 1h. Heating for 10min at 600W of microwave power to obtain the nitrogen-doped graphene material.
Example 3
(1) 1.0g of graphene oxide was weighed and dispersed in 30mL of 37% aqueous formaldehyde solution, and the dispersion was uniformly dispersed in an ultrasonic instrument and recorded as dispersion A.
(2) 10.0g of melamine is weighed and added into 40mL of deionized water, and the mixture is placed in an ultrasonic instrument to be uniformly dispersed by ultrasonic, and the dispersion liquid B is marked.
(3) Mixing the dispersion A and the dispersion B, heating in water bath to 70 ℃, and stirring for 10min. And adding triethanolamine into the reaction solution, adjusting the pH value of a reaction solution system to 8.0, ultrasonically mixing uniformly, pouring the reaction solution into a high-pressure reaction kettle, and heating to 120 ℃ for reaction for 12 hours. And (4) carrying out suction filtration and vacuum drying to obtain black solid powder.
(4) And (4) placing the black solid powder obtained in the step (3) in a microwave reaction chamber, and purging for 1h by 100mL/min argon. And heating for 20min at the microwave power of 600W to obtain the nitrogen-doped graphene material.
Example 4
(1) 1.0g of graphene oxide was weighed and dispersed in 30mL of 37% aqueous formaldehyde solution, and the dispersion was uniformly dispersed in an ultrasonic instrument and recorded as dispersion A.
(2) 10.0g of melamine is weighed and added into 40mL of deionized water, and the mixture is placed in an ultrasonic instrument and is uniformly dispersed by ultrasound to be marked as dispersion B.
(3) Mixing the dispersion A and the dispersion B, heating to 70 ℃ in a water bath, and stirring for 20min. And adding triethanolamine into the reaction solution, adjusting the pH value of a reaction solution system to 8.0, ultrasonically mixing uniformly, pouring the reaction solution into a high-pressure reaction kettle, and heating to 120 ℃ for reaction for 12 hours. And (4) carrying out suction filtration and vacuum drying to obtain black solid powder.
(4) And (4) placing the black solid powder obtained in the step (3) in a microwave reaction chamber, and purging with 100mL/min of argon for 1h. And heating for 30min at the microwave power of 600W to obtain the nitrogen-doped graphene material.
Example 5
(1) 1.0g of graphene oxide is weighed and dispersed in 30mL of 37% formaldehyde aqueous solution, and the obtained product is placed in an ultrasonic instrument and uniformly dispersed to obtain a dispersion A.
(2) 10.0g of melamine is weighed and added into 40mL of deionized water, and the mixture is placed in an ultrasonic instrument to be uniformly dispersed by ultrasonic, and the dispersion liquid B is marked.
(3) Mixing the dispersion A and the dispersion B, heating in water bath to 70 ℃, and stirring for 20min. And then adding potassium hydroxide into the reaction liquid, adjusting the pH value of a reaction liquid system to 9.0, carrying out ultrasonic mixing uniformly, then pouring the reaction liquid into a high-pressure reaction kettle, and heating to 120 ℃ for reaction for 12 hours. And (4) carrying out suction filtration and vacuum drying to obtain black solid powder.
(4) And (4) placing the black solid powder obtained in the step (3) in a microwave reaction chamber, and purging with 100mL/min of argon for 1h. Heating for 10min at the microwave power of 800W to obtain the nitrogen-doped graphene material.
Example 6
(1) 1.0g of graphene oxide was weighed and dispersed in 30mL of 37% aqueous formaldehyde solution, and the dispersion was uniformly dispersed in an ultrasonic instrument and recorded as dispersion A.
(2) 10.0g of melamine is weighed and added into 40mL of deionized water, and the mixture is placed in an ultrasonic instrument and is uniformly dispersed by ultrasound to be marked as dispersion B.
(3) Mixing the dispersion A and the dispersion B, heating to 80 ℃ in a water bath, and stirring for 30min. And then adding potassium hydroxide into the reaction liquid, adjusting the pH value of a reaction liquid system to 9.0, carrying out ultrasonic mixing uniformly, then pouring the reaction liquid into a high-pressure reaction kettle, and heating to 140 ℃ for reaction for 15 hours. And (4) carrying out suction filtration and vacuum drying to obtain black solid powder.
(4) And (4) placing the black solid powder obtained in the step (3) in a microwave reaction chamber, and purging with 100mL/min of argon for 1h. Heating for 10min at the microwave power of 800W to obtain the nitrogen-doped graphene material.
Example 7
(1) 1.0g of graphene oxide is weighed and dispersed in 30mL of 37% formaldehyde aqueous solution, and the obtained product is placed in an ultrasonic instrument and uniformly dispersed to obtain a dispersion A.
(2) 10.0g of melamine is weighed and added into 40mL of deionized water, and the mixture is placed in an ultrasonic instrument and is uniformly dispersed by ultrasound to be marked as dispersion B.
(3) Mixing the dispersion A and the dispersion B, heating to 80 ℃ in a water bath, and stirring for 30min. And adding triethanolamine into the reaction solution, adjusting the pH value of a reaction solution system to 9.0, ultrasonically mixing uniformly, pouring the reaction solution into a high-pressure reaction kettle, and heating to 160 ℃ for reaction for 15 hours. And (4) carrying out suction filtration and vacuum drying to obtain black solid powder.
(4) And (4) placing the black solid powder obtained in the step (3) in a microwave reaction chamber, and purging with 100mL/min of argon for 1h. Heating for 10min at the microwave power of 800W to obtain the nitrogen-doped graphene material.
Example 8
(1) 1.0g of graphene oxide is weighed and dispersed in 30mL of 37% formaldehyde aqueous solution, and the obtained product is placed in an ultrasonic instrument and uniformly dispersed to obtain a dispersion A.
(2) 10.0g of melamine is weighed and added into 40mL of deionized water, and the mixture is placed in an ultrasonic instrument to be uniformly dispersed by ultrasonic, and the dispersion liquid B is marked.
(3) Mixing the dispersion A and the dispersion B, heating in water bath to 80 ℃, and stirring for 30min. And adding triethanolamine into the reaction solution, adjusting the pH value of a reaction solution system to 9.0, ultrasonically mixing uniformly, pouring the reaction solution into a high-pressure reaction kettle, and heating to 160 ℃ for reacting for 18 hours. And (4) carrying out suction filtration and vacuum drying to obtain black solid powder.
(4) And (4) placing the black solid powder obtained in the step (3) in a microwave reaction chamber, and purging for 1h by 100mL/min argon. And heating for 30min at the microwave power of 1000W to obtain the nitrogen-doped graphene material.
An SEM image of the nitrogen-doped graphene material obtained in example 8 is shown in fig. 2, and it can be clearly seen that the nitrogen-doped graphene is a two-dimensional film, has a layered structure, and has some wrinkles on the surface.
Comparative example 1
In the step (1), formaldehyde solution is not used, and deionized water is used for replacing:
(1) 1.0g of graphene oxide is weighed and dispersed in 30mL of deionized water, and the obtained product is placed in an ultrasonic instrument and is uniformly dispersed, and the obtained product is marked as a dispersion liquid A.
(2) 10.0g of melamine is weighed and added into 40mL of deionized water, and the mixture is placed in an ultrasonic instrument and is uniformly dispersed by ultrasound to be marked as dispersion B.
(3) Mixing the dispersion A and the dispersion B, heating in water bath to 80 ℃, and stirring for 30min. And adding triethanolamine into the reaction solution, adjusting the pH value of a reaction solution system to 9.0, ultrasonically mixing uniformly, pouring the reaction solution into a high-pressure reaction kettle, and heating to 160 ℃ for reacting for 18 hours. And (4) carrying out suction filtration and vacuum drying to obtain black solid powder.
(4) And (4) placing the black solid powder obtained in the step (3) in a microwave reaction chamber, and purging for 1h by 100mL/min argon. Heating the graphene material for 30min at the microwave power of 1000W to obtain the comparative nitrogen-doped graphene material.
Comparative example 2
And (3) adjusting the pH value of the reaction solution without adding alkali liquor, and directly carrying out hydrothermal reaction after uniformly mixing the dispersion solution A and the dispersion solution B:
(1) 1.0g of graphene oxide is weighed and dispersed in 30mL of 37% formaldehyde aqueous solution, and the obtained product is placed in an ultrasonic instrument and uniformly dispersed to obtain a dispersion A.
(2) 10.0g of melamine is weighed and added into 40mL of deionized water, and the mixture is placed in an ultrasonic instrument to be uniformly dispersed by ultrasonic, and the dispersion liquid B is marked.
(3) And mixing the dispersion liquid A and the dispersion liquid B, uniformly mixing by ultrasonic waves, pouring the reaction liquid into a high-pressure reaction kettle, and heating to 160 ℃ for reacting for 18 hours. And (4) carrying out suction filtration and vacuum drying to obtain black solid powder.
(4) And (4) placing the black solid powder obtained in the step (3) in a microwave reaction chamber, and purging with 100mL/min of argon for 1h. Heating for 30min with 1000W of microwave power to obtain the contrast nitrogen-doped graphene material.
The materials of examples 1 to 8, comparative example 1 and comparative example 2 were used as negative electrode materials for lithium ion batteries. Taking the synthesized nitrogen-doped graphene as an active component, selecting a 2016 type battery shell, a metal lithium sheet (phi 16 mm multiplied by 1 mm), and 1.0M LiPF 6 The mixed solution of Ethylene Carbonate (EC)/diethyl carbonate (DEC) (volume ratio 1). The materials are assembled into a button cell in a glove box filled with Ar gas, and the test is carried out after the working electrode is fully soaked by the electrolyte. The method comprises the following five steps:
(1) Size mixing
The material used has a large specific surface and is easy to adsorb moisture in the air, so the material for preparing the electrode is firstly dried fully in a vacuum drying oven at 120 ℃ to remove the surface moisture. Then, adding an active substance, a conductive additive (acetylene black) and a binder (PVDF) into the dispersing agent according to the mass percentage of 80N-methylpyrrolidone (NMP) mixed grinding, resulting in uniform mixing of the materials, making a viscous slurry.
(2) Coating film
The resulting viscous paste was uniformly coated on a copper foil (thickness of about 100 μm). The specific operation is as follows: 1) The copper foil of appropriate size is cut and laid flat on a table top. 2) Removing stains on the surface of the copper foil. 3) The slurry was dispersed on a copper foil and the slurry was spread evenly on the copper foil using a die. 4) The copper foil coated with the slurry was dried in a vacuum drying oven at 120 ℃ for 12 hours.
(3) Rolling compaction
After the completion of drying, the copper foil coated with the slurry was rolled with a small-sized rolling machine to prevent the electrode material from falling off from the surface of the copper foil.
(4) Tabletting
And cutting the rolled film into a plurality of circular electrode slices with the diameter of 12mm by using a manual slicer. In order to prevent the coating film from falling off during charge and discharge cycles, it was pressed into a sheet by an oil press. And taking out and weighing after drying, and waiting for battery loading.
(5) Assembled battery
The process of assembling the button cells was carried out in a glove box filled with Ar gas. The battery is assembled according to the sequence of negative electrode battery shell/electrolyte/working electrode plate/electrolyte/diaphragm/lithium plate/positive electrode battery shell. And standing for 24 hours, and performing electrochemical test after the electrolyte is fully soaked.
And carrying out charge and discharge tests on the assembled button type simulation battery. The material of example 8 was used at a voltage in the range of 0.01 to 3.0V and at 100mA g -1 The results of the cycle stability test at the current density of (a) are shown in fig. 3. The contents of nitrogen elements in the electrode materials of examples 1 to 8 and comparative examples 1 to 2, the corresponding first charge-discharge capacity and the discharge capacity after 100 charge-discharge tests are shown in table 1. Wherein the content of nitrogen element is determined by element analysis.
TABLE 1
According to test data, the content of nitrogen doped in the graphene is improved, and the nitrogen content can reach 10.2% at most. Secondly, the specific capacity of the button cell for the first discharge is increased, and the maximum discharge capacity for the first discharge in the embodiment 8 can reach 425.8 mAh.g -1 Compared with the comparative example 1, the reversible capacity is improved by about 14%, and the reversible capacity is still kept higher after 100 times of circulation, the reversible capacity retention rate exceeds 80.0% and reaches 91.3% at most, which shows that the material prepared by the invention has higher reversible capacity and good cycle performance.