Method for synthesizing and collecting MXene material under assistance of organic solvent
阅读说明：本技术 一种有机溶剂辅助合成和收集MXene材料的方法 (Method for synthesizing and collecting MXene material under assistance of organic solvent ) 是由 吴巍炜 屈丹瑶 杜韬 胡文文 于 2021-07-19 设计创作，主要内容包括：本发明提供了一种有机溶剂辅助合成和收集MXene材料的方法,具体包括：1)将MXene前驱体(包括Ti-(3)AlC-(2)、Ti-(2)Al-(C)、Nb-(2)AlC、Mo-(2)Ga-(2)C、Cr-(2)TiAlC-(2)、Ti-(3)AlCN和(Nb-(0.8)Zr-(0.2))-(4)AlC-(3)中的任意一种)陶瓷粉末缓慢加入制备好的HCl溶液或LiF溶液中刻蚀,得到多层MXene材料；2)在多层MXene材料中加入二甲基亚砜插层剂进行搅拌插层；3)在二甲基亚砜和MXene材料的混合液中加入与水不互溶的插层剂的有机良溶剂洗涤,然后真空干燥；4)离心分离产物；5)得到的沉淀物重复2)-4)的操作,共循环4-8次。6)通过冷冻干燥便可得到多种尺寸的MXene材料,并随着循环次数的增加,产物的尺寸逐渐变大。本发明不仅能够可控合成不同尺寸的MXene材料纳米片,还可以大幅度提升MXene材料的产率。(The invention provides a method for synthesizing and collecting MXene materials under the assistance of an organic solvent, which specifically comprises the following steps: 1) mixing MXene precursor (including Ti) 3 AlC 2 、Ti 2 Al C 、Nb 2 AlC、Mo 2 Ga 2 C、Cr 2 TiAlC 2 、Ti 3 AlCN and (Nb) 0.8 Zr 0.2 ) 4 AlC 3 Any one of the above) ceramic powder is slowly added into the prepared HCl solution or LiF solution for etchingEtching to obtain a multilayer MXene material; 2) adding a dimethyl sulfoxide intercalation agent into the multilayer MXene material for stirring and intercalation; 3) adding an organic good solvent of an intercalation agent which is not mutually soluble with water into the mixed solution of dimethyl sulfoxide and MXene materials for washing, and then carrying out vacuum drying; 4) centrifuging the product; 5) the obtained precipitate is subjected to the operations 2) to 4) repeatedly, and is circulated for 4 to 8 times. 6) MXene materials of various sizes were obtained by freeze drying, and the product size gradually increased with increasing cycle number. The method can be used for controllably synthesizing MXene material nanosheets of different sizes, and can also be used for greatly improving the yield of the MXene material.)
1. A method for synthesizing and collecting MXene materials by assistance of organic solvents is characterized by comprising the following steps:
1) firstly, mixing 10-30 mL of HCl solution and 0.8-2 g of LiF to generate HF in situ, wherein the concentration of the HCl solution is 6-15M, and then slowly adding 0.5-2 g of MXene precursor ceramic powder into the mixture to perform stirring reaction to obtain a multilayer MXene, wherein the reaction temperature is 20-60 ℃, and the stirring speed is 500 rpm;
2) adding dimethyl sulfoxide intercalation agent into the multiple layers of MXene to carry out stirring intercalation;
3) after intercalation, adding an organic good solvent of an intercalating agent which is immiscible with water into the mixed solution of dimethyl sulfoxide and MXene for centrifugal washing, and then carrying out vacuum drying;
4) centrifuging the product;
5) repeating the operations 2) -4) on the precipitate obtained in the step 1), and performing circulation for 4-8 times to maximally squeeze the product;
6) MXene products of different sizes were obtained by freeze drying.
2. The organic solvent assisted method for synthesizing and collecting MXene materials as claimed in claim 1, wherein: the precursor ceramic powder of MXene in the step 1) is Ti3AlC2、Ti2AlC、Nb2AlC、Mo2Ga2C、Cr2TiAlC2、Ti3AlCN and (Nb)0.8Zr0.2)4AlC3Any one of them.
3. The organic solvent assisted synthesis and collection of MXene materials of claim 1 or 2, wherein: the etching time of the MXene precursor ceramic powder in the HF generated in situ by mixing HCl and LiF in the step 1) is 12-50 h.
4. The method for organic solvent assisted synthesis and collection of MXene materials according to claim 3, wherein: the feeding ratio of the multiple layers of MXene and dimethyl sulfoxide in the step 2) is 0.2-5 g: 10-50 mL, and the stirring and intercalation time is 1-24 h.
5. The organic solvent assisted synthesis and collection of MXene materials of claim 1 or 4, wherein: the volume ratio of the good organic solvent of the water-immiscible intercalating agent in the step 3) to the dimethyl sulfoxide is 1: 1, the rotation speed of centrifugal washing is 1000-.
6. The method for organic solvent assisted synthesis and collection of MXene materials according to claim 5, wherein: the good organic solvent of the water-immiscible intercalating agent in the step 3) is dichloromethane or carbon tetrachloride or trichloromethane or dichloroethane or methyl ethyl ketone or toluene or xylene.
7. The organic solvent assisted synthesis and collection of MXene materials of claim 1 or 6, wherein: the vacuum drying time in the step 3) is 1-3 h.
8. The organic solvent assisted method for synthesizing and collecting MXene materials of claim 7, wherein: the centrifugation speed for separating the products in the step 4) is 2000-4000 rpm, and the centrifugation time is 15-60 min.
9. The organic solvent assisted synthesis and collection of MXene materials of claim 1 or 8, wherein: the freeze-drying time in the step 6) is 12-36 h.
Technical Field
The invention belongs to the technical field of MXene synthesis, and particularly relates to a method for synthesizing and collecting MXene under the assistance of an organic solvent.
Background
MXene materials are leading-edge two-dimensional nanomaterials and have a wide range of potential applications including electromagnetic interference shielding, electrochemical energy storage, catalysis, sensors, biomedicine and the like. As an important cornerstone for these applications, many researchers are currently focusing on the study of synthetic methods that meet the needs of industrial applications or large scale. A good nano material synthesis method requires good controllability, high yield, low cost, green process, safety and the like, which are main factors for determining whether a synthesis method can be separated from laboratory demonstration and enter mass production. In the development of MXene materials, new synthetic methods are continuously emerging. Initially, MXene materials were prepared in a two-step process, first etching the MAX phase with hydrofluoric acid HF and then embedding the multilayer sheet with organic molecules (e.g., hydrazine, urea, and dimethyl sulfoxide). But the use of hydrofluoric acid not only carries a risk, but the low yield (less than 20%) further indicates that it is not possible to use for large-scale production. Later, a more gentle etch system using fluoride salt LiF mixed with HCl was reported. In this system, HF is formed in situ to give a multilayer MXene material, and then after sonication in water, a submicron single layer MXene flake can be obtained, although the use of HF is avoided, the resulting MXene flake is small in size and low in yield. Recently, there have been some related studies to increase the yield or size of MXene flakes. However, it still has certain challenges to meet all the above requirements, including synthesis controllability, high yield, low cost, green process, safety, etc.
Disclosure of Invention
The invention aims to solve the technical problem of providing a milder and more convenient method for synthesizing and collecting MXene materials under the assistance of an organic solvent aiming at the problems in the prior art, and the MXene materials with controllable size and improved yield are obtained.
The technical scheme is as follows for solving the technical problem of the invention:
a method for organic solvent assisted synthesis and collection of MXene material comprising the steps of:
1) firstly, mixing 10-30 mL of HCl solution and 0.8-2 g of LiF to generate HF in situ, wherein the concentration of the HCl solution is 6-15M, and then slowly adding 0.5-2 g of MXene precursor ceramic powder into the mixture to perform stirring reaction to obtain a multilayer MXene, wherein the reaction temperature is 20-60 ℃, and the stirring speed is 500 rpm;
2) adding dimethyl sulfoxide intercalation agent into the multiple layers of MXene to carry out stirring intercalation;
3) after intercalation, adding an organic good solvent of an intercalating agent which is immiscible with water into the mixed solution of dimethyl sulfoxide and MXene for centrifugal washing, and then carrying out vacuum drying;
4) centrifuging the product;
5) repeating the operations 2) -4) on the precipitate obtained in the step 1), and performing circulation for 4-8 times to maximally squeeze the product;
6) MXene products of different sizes were obtained by freeze drying.
The precursor ceramic powder of MXene in the step 1) is Ti3AlC2、Ti2AlC、Nb2AlC、Mo2Ga2C、Cr2TiAlC2、Ti3AlCN and (Nb)0.8Zr0.2)4AlC3Any one of them.
The etching time of the MXene precursor ceramic powder in the HF generated in situ by mixing HCl and LiF in the step 1) is 12-50 h.
The feeding ratio of the multiple layers of MXene and dimethyl sulfoxide in the step 2) is 0.2-5 g: 10-50 mL, and the stirring and intercalation time is 1-24 h.
The volume ratio of the good organic solvent of the water-immiscible intercalating agent in the step 3) to the dimethyl sulfoxide is 1: 1, the rotation speed of centrifugal washing is 1000-.
The good organic solvent of the water-immiscible intercalating agent in the step 3) is dichloromethane or carbon tetrachloride or trichloromethane or dichloroethane or methyl ethyl ketone or toluene or xylene.
The vacuum drying time in the step 3) is 1-3 h.
The centrifugation speed for separating the products in the step 4) is 2000-4000 rpm, and the centrifugation time is 15-60 min.
The freeze-drying time in the step 6) is 12-36 h.
The invention provides a method for synthesizing and collecting MXene materials under the assistance of an organic solvent, which adopts a method of intercalation collection under the assistance of the organic solvent, namely a dimethyl sulfoxide intercalation is utilized, an organic good solvent of an intercalating agent which is immiscible with water is utilized to remove the dimethyl sulfoxide and collect a product, the whole process has no ultrasonic treatment, and a centrifugal speed of more than 4000rpm is not used, so that MXene nanosheets with different sizes can be controllably synthesized, and the yield of the MXene materials can be greatly improved. Compared with the prior art, the invention has the following advantages: (1) in the invention, dimethyl sulfoxide is used for intercalation, organic good solvent of an intercalating agent immiscible with water is used for washing and collecting a product, and one of the products MXene Ti is obtained by using the method3C2TxThe yield of the product is improved to 46.3 percent. (2) The organic good solvent of the intercalation agent which is not mutually soluble with water is added when the product is collected, so that the requirement of experimental equipment is reduced, and the centrifugal speed in the whole process is lower than 4000 rpm. (3) The MXene sheets with different sizes can be prepared by repeating the operations of intercalation, product collection and the like for multiple times. (4) MXene Ti prepared by the invention3C2TxThe film had good conductivity (8672S cm-1) and excellent capacitance performance (352F g-1).
Drawings
FIG. 1 shows MXene Ti as a product of 1 cycle of step 5) in example 1 of the present invention3C2TxTEM images corresponding to the lamella;
FIG. 2 shows the step 5) of example 1 of the present invention being cycled 2 timesProduct MXene Ti3C2TxTEM images corresponding to the lamella;
FIG. 3 shows MXene Ti as a product of 3 cycles of step 5) in example 1 of the present invention3C2TxTEM images corresponding to the lamella;
FIG. 4 shows MXene Ti as a product of 4 cycles of step 5) in example 1 of the present invention3C2TxTEM images corresponding to the lamella;
FIG. 5 shows MXene Ti as a product of 5 cycles of step 5) in example 1 of the present invention3C2TxTEM images corresponding to the lamella;
FIG. 6 shows MXene Ti as a product of 6 cycles of step 5) in example 1 of the present invention3C2TxTEM images corresponding to the lamella;
FIG. 7 shows MXene Ti obtained in step 5) 6 cycles of example 13C2TxRespectively corresponding average area histograms;
FIG. 8 shows MXene Ti in 6 cycles of step 5) in example 1 of the present invention3C2TxHistogram of yield of (c).
Detailed Description
In order to make the contents, technical solutions and advantages of the present invention more apparent, the present invention is further described below with reference to specific embodiments and drawings, and these embodiments are merely used to illustrate the present invention, and the present invention is not limited to the following embodiments.
Example 1
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, mixing 20mL of 9M HCl solution with 1g of LiF to generate HF in situ, and mixing 1g of Ti3AlC2Slowly adding ceramic powder, etching for 24h at 35 ℃ and with the stirring speed of 350rpm, and then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain multilayer MXene Ti3C2Tx；
2) In multiple layers of MXene Ti3C2TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethylSulfoxide and MXene Ti3C2TxThe volume ratio of the mixed solution of (1): 1, adding dichloromethane for washing (centrifugal washing, 2000 rpm), washing with dichloromethane at least three times, and after dimethyl sulfoxide in the MXene solution is basically removed, drying in vacuum at room temperature for 2 hours to remove residual dichloromethane;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti3C2TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Obtaining MXene Ti with 6 sizes by respectively freeze drying3C2TxThe size of the product gradually increased with increasing number of cycles (0.47 μm)2 ～ 4.60 μm2) The yield after 6 cycles was 46.3%, good conductivity (8672S cm-1) and excellent capacitance performance (352F g-1).
Example 2
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, mixing 20mL of 9M HCl solution with 1g of LiF to generate HF in situ, and mixing 1g of Ti3AlC2Slowly adding ceramic powder, etching for 24h at 35 ℃ and with the stirring speed of 350rpm, and then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain multilayer MXene Ti3C2Tx；
2) In multiple layers of MXene Ti3C2TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti3C2TxThe volume ratio of the mixed solution of (1): 1, adding carbon tetrachloride for washing (centrifugal washing, 2000 rpm), washing with carbon tetrachloride for at least three times, and after dimethyl sulfoxide in the MXene solution is basically removed, carrying out vacuum drying for 2 hours to remove residual carbon tetrachloride;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti3C2TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Respectively freeze-drying to obtain 6 MXene Ti powders with gradually increased sizes3C2TxAnd (3) obtaining the product.
Example 3
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, mixing 20mL of 9M HCl solution with 1g of LiF to generate HF in situ, and mixing 1g of Ti3AlC2Slowly adding ceramic powder, etching for 24h at 35 ℃ and with the stirring speed of 350rpm, and then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain multilayer MXene Ti3C2Tx；
2) In multiple layers of MXene Ti3C2TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti3C2TxThe volume ratio of the mixed solution of (1): 1, adding trichloromethane for washing (centrifugal washing, 2000 rpm), washing with trichloromethane for at least three times, and after dimethyl sulfoxide in the MXene solution is basically removed, carrying out vacuum drying for 2 hours to remove residual trichloromethane;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti3C2TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Respectively freeze-drying to obtain 6 MXene Ti powders with gradually increased sizes3C2TxAnd (3) obtaining the product.
Example 4
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, mixing 20mL of 9M HCl solution with 1g of LiF to generate HF in situ, and mixing 1g of Ti3AlC2Ceramic materialSlowly adding the powder, etching for 24h at 35 ℃ and with the stirring speed of 350rpm, and then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a multilayer MXene Ti3C2Tx；
2) In multiple layers of MXene Ti3C2TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti3C2TxThe volume ratio of the mixed solution of (1): 1, adding dichloroethane for washing (centrifugal washing, 2000 rpm), washing with dichloroethane at least three times until dimethyl sulfoxide in the MXene solution is basically removed, and then drying in vacuum for 2 hours to remove residual dichloroethane;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti3C2TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Respectively freeze-drying to obtain 6 MXene Ti powders with gradually increased sizes3C2TxAnd (3) obtaining the product.
Example 5
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, mixing 20mL of 9M HCl solution with 1g of LiF to generate HF in situ, and mixing 1g of Ti3AlC2Slowly adding ceramic powder, etching for 24h at 35 ℃ and with the stirring speed of 350rpm, and then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain multilayer MXene Ti3C2Tx；
2) In multiple layers of MXene Ti3C2TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti3C2TxThe volume ratio of the mixed solution of (1): 1, adding methyl ethyl ketone for washing (centrifugal washing, 2000 rpm), and washing with methyl ethyl ketone at least three times until dimethyl is added into MXene solutionAfter the sulfoxide is basically removed, vacuum drying is carried out for 2 hours to remove the residual methyl ethyl ketone;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti3C2TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Respectively freeze-drying to obtain 6 MXene Ti powders with gradually increased sizes3C2TxAnd (3) obtaining the product.
Example 6
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, mixing 20mL of 9M HCl solution with 1g of LiF to generate HF in situ, and mixing 1g of Ti3AlC2Slowly adding ceramic powder, etching for 24h at 35 ℃ and with the stirring speed of 350rpm, and then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain multilayer MXene Ti3C2Tx；
2) In multiple layers of MXene Ti3C2TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti3C2TxThe volume ratio of the mixed solution of (1): 1, adding toluene for washing (centrifugal washing, 2000 rpm), washing with toluene for at least three times, and after dimethyl sulfoxide in the MXene solution is basically removed, carrying out vacuum drying for 2 hours to remove residual toluene;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti3C2TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Respectively freeze-drying to obtain 6 MXene Ti powders with gradually increased sizes3C2TxAnd (3) obtaining the product.
Example 7
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, mixing 20mL of 9M HCl solution with 1g of LiF to generate HF in situ, and mixing 1g of Ti3AlC2Slowly adding ceramic powder, etching for 24h at 35 ℃ and with the stirring speed of 350rpm, and then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain multilayer MXene Ti3C2Tx；
2) In multiple layers of MXene Ti3C2TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti3C2TxThe volume ratio of the mixed solution of (1): 1, adding dimethylbenzene for washing (centrifugal washing, 2000 rpm), washing with dimethylbenzene for at least three times, and after dimethyl sulfoxide in the MXene solution is basically removed, carrying out vacuum drying for 2 hours to remove residual dimethylbenzene;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti3C2TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Respectively freeze-drying to obtain 6 MXene Ti powders with gradually increased sizes3C2TxAnd (3) obtaining the product.
Example 8
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first 20mL of 4M HCl solution was mixed with 2.07g LiF to generate HF in situ, and 0.5g Ti was added2Slowly adding AlC ceramic powder into the HCl/LiF mixed solution prepared in advance, and etching for 48 hours at the temperature of 50 ℃ and at the stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a plurality of layers of MXene Ti2CTx；
2) In multiple layers of MXene Ti2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti2CTxThe volume ratio of the mixed solution of (1): 1 ratio, washing with dichloromethane (centrifugal washing, 1000 rpm) at least three times to MXene Ti2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual dichloromethane;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was subjected to the operations of 2) to 4) repeatedly for 8 cycles.
6) Obtaining 8 MXene Ti with gradually increased sizes by freeze drying2CTxAnd (3) obtaining the product.
Example 9
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first 20mL of 4M HCl solution was mixed with 2.07g LiF to generate HF in situ, and 0.5g Ti was added2Slowly adding AlC ceramic powder into the HCl/LiF mixed solution prepared in advance, and etching for 48 hours at the temperature of 50 ℃ and at the stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a plurality of layers of MXene Ti2CTx；
2) In multiple layers of MXene Ti2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti2CTxThe volume ratio of the mixed solution of (1): 1 is washed at least three times by adding carbon tetrachloride (centrifugal washing, 1000 rpm) until MXene Ti is obtained2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual carbon tetrachloride;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was subjected to the operations of 2) to 4) repeatedly for 8 cycles.
6) Obtaining 8 MXene Ti with gradually increased sizes by freeze drying2CTxAnd (3) obtaining the product.
Example 10
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first 20mL of 4M HCl solution was mixed with 2.07g LiF to generate HF in situ, and 0.5g Ti was added2Slowly adding AlC ceramic powder into the HCl/LiF mixed solution prepared in advance, and etching for 48 hours at the temperature of 50 ℃ and at the stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a plurality of layers of MXene Ti2CTx；
2) In multiple layers of MXene Ti2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti2CTxThe volume ratio of the mixed solution of (1): 1 is added with chloroform for washing (centrifugal washing, 1000 rpm) for at least three times until MXene Ti2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual trichloromethane;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was subjected to the operations of 2) to 4) repeatedly for 8 cycles.
6) Obtaining 8 MXene Ti with gradually increased sizes by freeze drying2CTxAnd (3) obtaining the product.
Example 11
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first 20mL of 4M HCl solution was mixed with 2.07g LiF to generate HF in situ, and 0.5g Ti was added2Slowly adding AlC ceramic powder into the HCl/LiF mixed solution prepared in advance, and etching for 48 hours at the temperature of 50 ℃ and at the stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a plurality of layers of MXene Ti2CTx；
2) In multiple layers of MXene Ti2CTxAccording to 1 g: feed ratio of 20mLAdding dimethyl sulfoxide, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti2CTxThe volume ratio of the mixed solution of (1): 1 is washed at least three times by adding dichloroethane (centrifugal washing, 1000 rpm) to MXene Ti2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual dichloroethane;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the obtained precipitate was subjected to the operations 2) to 4) repeatedly for 8 cycles.
6) Obtaining 8 MXene Ti with gradually increased sizes by freeze drying2CTxAnd (3) obtaining the product.
Example 12
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first 20mL of 4M HCl solution was mixed with 2.07g LiF to generate HF in situ, and 0.5g Ti was added2Slowly adding AlC ceramic powder into the HCl/LiF mixed solution prepared in advance, and etching for 48 hours at the temperature of 50 ℃ and at the stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a plurality of layers of MXene Ti2CTx；
2) In multiple layers of MXene Ti2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti2CTxThe volume ratio of the mixed solution of (1): 1, adding methyl ethyl ketone for washing (centrifugal washing, 1000 rpm) for at least three times until MXene Ti2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual methyl ethyl ketone;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was subjected to the operations of 2) to 4) repeatedly for 8 cycles.
6) Obtaining 8 MXene Ti with gradually increased sizes by freeze drying2CTxAnd (3) obtaining the product.
Example 13
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first 20mL of 4M HCl solution was mixed with 2.07g LiF to generate HF in situ, and 0.5g Ti was added2Slowly adding AlC ceramic powder into the HCl/LiF mixed solution prepared in advance, and etching for 48 hours at the temperature of 50 ℃ and at the stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a plurality of layers of MXene Ti2CTx；
2) In multiple layers of MXene Ti2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti2CTxThe volume ratio of the mixed solution of (1): 1 ratio of toluene to MXene Ti (centrifugal washing, 1000 rpm) for at least three times2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual toluene;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was subjected to the operations of 2) to 4) repeatedly for 8 cycles.
6) Obtaining 8 MXene Ti with gradually increased sizes by freeze drying2CTxAnd (3) obtaining the product.
Example 14
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first 20mL of 4M HCl solution was mixed with 2.07g LiF to generate HF in situ, and 0.5g Ti was added2Slowly adding AlC ceramic powder into the HCl/LiF mixed solution prepared in advance, and etching for 48 hours at the temperature of 50 ℃ and at the stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a plurality of layers of MXene Ti2CTx；
2) In multiple layers of MXene Ti2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti2CTxThe volume ratio of the mixed solution of (1): 1 ratio of xylene washing (centrifugal washing, 1000 rpm) at least three times to MXene Ti2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual xylene;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was subjected to the operations of 2) to 4) repeatedly for 8 cycles.
6) Obtaining 8 MXene Ti with gradually increased sizes by freeze drying2CTxAnd (3) obtaining the product.
Example 15
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, 30 mL of 6M HCl solution is mixed with 1.98g of LiF to generate HF in situ, and 3g of Nb is added2Slowly adding AlC ceramic powder, etching for 45h at 40 ℃ under the condition that the stirring speed is 350rpm, and then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a multilayer MXene Nb2CTx；
2) In multiple layers of MXene Nb2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 24h, and intercalating;
3) in dimethyl sulfoxide and MXene Nb2CTxThe volume ratio of the mixed solution of (1): 1 ratio, adding dichloromethane for washing (centrifugal washing, 4000 rpm) for at least three times until MXene Nb2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual dichloromethane;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Nb2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the obtained precipitate was subjected to the operations 2) to 4) repeatedly for 6 cycles.
6) Obtaining 6 MXene Nb with gradually enlarged size by freeze drying2CTxAnd (3) obtaining the product.
Example 16
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, 30 mL of 6M HCl solution is mixed with 1.98g of LiF to generate HF in situ, and 3g of Nb is added2Slowly adding AlC ceramic powder, etching for 45h at 40 ℃ under the condition that the stirring speed is 350rpm, and then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a multilayer MXene Nb2CTx；
2) In multiple layers of MXene Nb2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 24h, and intercalating;
3) in dimethyl sulfoxide and MXene Nb2CTxThe volume ratio of the mixed solution of (1): 1 is added with carbon tetrachloride for washing (centrifugal washing, 1000 rpm) for at least three times until MXene Nb is obtained2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual carbon tetrachloride;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Nb2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Obtaining 6 MXene Nb with gradually enlarged size by freeze drying2CTxAnd (3) obtaining the product.
Example 17
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, 30 mL of 6M HCl solution is mixed with 1.98g of LiF to generate HF in situ, and 3g of Nb is added2Slowly adding AlC ceramic powder, etching for 45h at 40 ℃ under the condition that the stirring speed is 350rpm, and then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a multilayer MXene Nb2CTx；
2) In multiple layers of MXene Nb2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 24h, and intercalating;
3) in dimethyl sulfoxide and MXene Nb2CTxThe volume ratio of the mixed solution of (1): 1 is added with chloroform for washing (centrifugal washing, 4000 rpm) for at least three times until MXene Nb2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual trichloromethane;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Nb2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Obtaining 6 MXene Nb with gradually enlarged size by freeze drying2CTxAnd (3) obtaining the product.
Example 18
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, 30 mL of 6M HCl solution is mixed with 1.98g of LiF to generate HF in situ, and 3g of Nb is added2Slowly adding AlC ceramic powder, etching for 45h at 40 ℃ under the condition that the stirring speed is 350rpm, and then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a multilayer MXene Nb2CTx；
2) In multiple layers of MXene Nb2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 24h, and intercalating;
3) in dimethyl sulfoxide and MXene Nb2CTxThe volume ratio of the mixed solution of (1): 1 is washed at least three times by adding dichloroethane (centrifugal washing, 4000 rpm) until MXene Nb is obtained2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual dichloroethane;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Nb2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Obtaining 6 MXene Nb with gradually enlarged size by freeze drying2CTxAnd (3) obtaining the product.
Example 19
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, 30 mL of 6M HCl solution is mixed with 1.98g of LiF to generate HF in situ, and 3g of Nb is added2Slowly adding AlC ceramic powder, etching for 45h at 40 ℃ under the condition that the stirring speed is 350rpm, and then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a multilayer MXene Nb2CTx；
2) In multiple layers of MXene Nb2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 24h, and intercalating;
3) in dimethyl sulfoxide and MXene Nb2CTxThe volume ratio of the mixed solution of (1): 1, adding methyl ethyl ketone for washing (centrifugal washing, 4000 rpm) for at least three times until MXene Nb is obtained2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual methyl ethyl ketone;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Nb2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Obtaining 6 MXene Nb with gradually enlarged size by freeze drying2CTxAnd (3) obtaining the product.
Example 20
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, 30 mL of 6M HCl solution is mixed with 1.98g of LiF to generate HF in situ, and 3g of Nb is added2Slowly adding AlC ceramic powder, etching for 45h at 40 ℃ under the condition that the stirring speed is 350rpm, and then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a multilayer MXene Nb2CTx；
2) In multiple layers of MXene Nb2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 24h, and intercalating;
3) in dimethyl sulfoxide and MXene Nb2CTxThe volume ratio of the mixed solution of (1): 1 ratio, adding toluene for washing (centrifugal washing, 4000 rpm) at least three times until MXene Nb2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual toluene;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Nb2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Obtaining 6 MXene Nb with gradually enlarged size by freeze drying2CTxAnd (3) obtaining the product.
Example 21
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, 30 mL of 6M HCl solution is mixed with 1.98g of LiF to generate HF in situ, and 3g of Nb is added2Slowly adding AlC ceramic powder, etching for 45h at 40 ℃ under the condition that the stirring speed is 350rpm, and then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a multilayer MXene Nb2CTx；
2) In multiple layers of MXene Nb2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 24h, and intercalating;
3) in dimethyl sulfoxide and MXene Nb2CTxThe volume ratio of the mixed solution of (1): 1, adding xylene to wash (centrifugal washing, 4000 rpm) for at least three times until MXene Nb is obtained2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual xylene;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Nb2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Obtaining 6 MXene Nb with gradually enlarged size by freeze drying2CTxAnd (3) obtaining the product.
Example 22
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, 20mL of 12M HCl solution is mixed with 3M LiF to generate HF in situ, and 1g of Mo is added2Ga2C ceramic powder is slowly added and etched at 35 ℃ and a stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain multilayer MXene Mo2CTx；
2) In multiple layers of MXene Mo2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Mo2CTxThe volume ratio of the mixed solution of (1): 1 ratio, washing with dichloromethane (centrifugal washing, 2000 rpm) at least three times to obtain MXene Mo2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual dichloromethane;
4) adding a proper amount of deionized water, and carrying out vortex oscillation to disperse MXene Mo2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 4 times.
6) 4 MXene Mo with gradually increased sizes can be obtained by freeze drying2CTxAnd (3) obtaining the product.
Example 23
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, 20mL of 12M HCl solution is mixed with 3M LiF to generate HF in situ, and 1g of Mo is added2Ga2C ceramic powder is slowly added and etched at 35 ℃ and a stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain multilayer MXene Mo2CTx；
2) In multiple layers of MXene Mo2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Mo2CTxThe volume ratio of the mixed solution of (1): 1 is added with carbon tetrachloride for washing (centrifugal washing, 2000 rpm) for at least three times until MXene Mo2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual carbon tetrachloride;
4) adding a proper amount of deionized water, and carrying out vortex oscillation to disperse MXene Mo2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 4 times.
6) 4 MXene Mo with gradually increased sizes can be obtained by freeze drying2CTxAnd (3) obtaining the product.
Example 24
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, 20mL of 12M HCl solution is mixed with 3M LiF to generate HF in situ, and 1g of Mo is added2Ga2C ceramic powder is slowly added and etched at 35 ℃ and a stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain multilayer MXene Mo2CTx；
2) In multiple layers of MXene Mo2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Mo2CTxThe volume ratio of the mixed solution of (1): 1 is added with chloroform for washing (centrifugal washing, 2000 rpm) for at least three times until MXene Mo2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual trichloromethane;
4) adding a proper amount of deionized water, and carrying out vortex oscillation to disperse MXene Mo2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 4 times.
6) 4 MXene Mo with gradually increased sizes can be obtained by freeze drying2CTxAnd (3) obtaining the product.
Example 25
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, 20mL of 12M HCl solution is mixed with 3M LiF to generate HF in situ, and 1g of Mo is added2Ga2C ceramic powder is slowly added and etched at 35 ℃ and a stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain multilayer MXene Mo2CTx；
2) In multiple layers of MXene Mo2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Mo2CTxThe volume ratio of the mixed solution of (1): 1 is added with dichloroethane for washing (centrifugal washing, 2000 rpm) at least three times until MXene Mo2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual dichloroethane;
4) adding a proper amount of deionized water, and carrying out vortex oscillation to disperse MXene Mo2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 4 times.
6) 4 MXene Mo with gradually increased sizes can be obtained by freeze drying2CTxAnd (3) obtaining the product.
Example 26
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, 20mL of 12M HCl solution is mixed with 3M LiF to generate HF in situ, and 1g of Mo is added2Ga2C ceramic powder is slowly added and etched at 35 ℃ and a stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain multilayer MXene Mo2CTx；
2) In multiple layers of MXene Mo2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Mo2CTxThe volume ratio of the mixed solution of (1): 1, adding methyl ethyl ketone to wash (centrifugal washing, 2000 rpm) for at least three times until MXene Mo2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual methyl ethyl ketone;
4) adding a proper amount of deionized water, and carrying out vortex oscillation to disperse MXene Mo2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 4 times.
6) 4 MXene Mo with gradually increased sizes can be obtained by freeze drying2CTxAnd (3) obtaining the product.
Example 27
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, 20mL of 12M HCl solution is mixed with 3M LiF to generate HF in situ, and 1g of Mo is added2Ga2C ceramic powder is slowly added and etched at 35 ℃ and a stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain multilayer MXene Mo2CTx；
2) In multiple layers of MXene Mo2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Mo2CTxThe volume ratio of the mixed solution of (1): 1 ratio of toluene is added for washing (centrifugal washing, 2000 rpm) for at least three times until MXene Mo2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual toluene;
4) adding a proper amount of deionized water, and carrying out vortex oscillation to disperse MXene Mo2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and circulated 4 times.
6) 4 MXene Mo with gradually increased sizes can be obtained by freeze drying2CTxAnd (3) obtaining the product.
Example 28
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, 20mL of 12M HCl solution is mixed with 3M LiF to generate HF in situ, and 1g of Mo is added2Ga2C ceramic powder is slowly added and etched at 35 ℃ and a stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain multilayer MXene Mo2CTx；
2) In multiple layers of MXene Mo2CTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Mo2CTxThe volume ratio of the mixed solution of (1): 1, adding xylene to wash (centrifugal washing, 2000 rpm) for at least three times until MXene Mo2CTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual xylene;
4) adding a proper amount of deionized water, and carrying out vortex oscillation to disperse MXene Mo2CTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 4 times.
6) 4 MXene Mo with gradually increased sizes can be obtained by freeze drying2CTxAnd (3) obtaining the product.
Example 29
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first, 20mL of 6M HCl solution was mixed with 1.28g LiF to generate HF in situ, and 2g of Cr was added2TiAlC2The ceramic powder was slowly added and etched for 42h at 55 ℃ with a stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a multilayer MXene Cr2TiC2Tx；
2) In multiple layers of MXene Cr2TiC2TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Cr2TiC2TxThe volume ratio of the mixed solution of (1): 1 ratio, adding dichloromethane for washing (centrifugal washing, 2000 rpm) for at least three times until MXene Cr2TiC2TxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual dichloromethane;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Cr2TiC2TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) 6 MXene Cr with gradually increased size can be obtained by freeze drying2TiC2TxAnd (3) obtaining the product.
Example 30
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first, 20mL of 6M HCl solution was mixed with 1.28g LiF to generate HF in situ, and 2g of Cr was added2TiAlC2The ceramic powder was slowly added and etched for 42h at 55 ℃ with a stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a multilayer MXene Cr2TiC2Tx；
2) In multiple layers of MXene Cr2TiC2TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Cr2TiC2TxThe volume ratio of the mixed solution of (1): 1 is added with carbon tetrachloride for washing (centrifugal washing, 2000 rpm) for at least three times until MXene Cr is obtained2TiC2TxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual carbon tetrachloride;
4) adding proper amount ofIonized water and vortex vibration to disperse MXene Cr2TiC2TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) 6 MXene Cr with gradually increased size can be obtained by freeze drying2TiC2TxAnd (3) obtaining the product.
Example 31
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first, 20mL of 6M HCl solution was mixed with 1.28g LiF to generate HF in situ, and 2g of Cr was added2TiAlC2The ceramic powder was slowly added and etched for 42h at 55 ℃ with a stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a multilayer MXene Cr2TiC2Tx；
2) In multiple layers of MXene Cr2TiC2TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Cr2TiC2TxThe volume ratio of the mixed solution of (1): 1 is added with trichloromethane for washing (centrifugal washing, 2000 rpm) for at least three times until MXene Cr2TiC2TxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual trichloromethane;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Cr2TiC2TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) 6 MXene Cr with gradually increased size can be obtained by freeze drying2TiC2TxAnd (3) obtaining the product.
Example 32
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first dissolve 20mL of 6M HClThe solution was mixed with 1.28g LiF to generate HF in situ, 2g Cr2TiAlC2The ceramic powder was slowly added and etched for 42h at 55 ℃ with a stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a multilayer MXene Cr2TiC2Tx；
2) In multiple layers of MXene Cr2TiC2TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Cr2TiC2TxThe volume ratio of the mixed solution of (1): 1 is added with dichloroethane for washing (centrifugal washing, 2000 rpm) at least three times until MXene Cr2TiC2TxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual dichloroethane;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Cr2TiC2TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) 6 MXene Cr with gradually increased size can be obtained by freeze drying2TiC2TxAnd (3) obtaining the product.
Example 33
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first, 20mL of 6M HCl solution was mixed with 1.28g LiF to generate HF in situ, and 2g of Cr was added2TiAlC2The ceramic powder was slowly added and etched for 42h at 55 ℃ with a stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a multilayer MXene Cr2TiC2Tx；
2) In multiple layers of MXene Cr2TiC2TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Cr2TiC2TxThe volume ratio of the mixed solution of (1): 1 ofAdding methyl ethyl ketone in proportion for washing (centrifugal washing, 2000 rpm) for at least three times until MXene Cr2TiC2TxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual methyl ethyl ketone;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Cr2TiC2TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the obtained precipitate was subjected to the operations 2) to 4) repeatedly for 6 cycles.
6) 6 MXene Cr with gradually increased size can be obtained by freeze drying2TiC2TxAnd (3) obtaining the product.
Example 34
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first, 20mL of 6M HCl solution was mixed with 1.28g LiF to generate HF in situ, and 2g of Cr was added2TiAlC2The ceramic powder was slowly added and etched for 42h at 55 ℃ with a stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a multilayer MXene Cr2TiC2Tx；
2) In multiple layers of MXene Cr2TiC2TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Cr2TiC2TxThe volume ratio of the mixed solution of (1): 1 ratio of toluene is added for washing (centrifugal washing, 2000 rpm) for at least three times until MXene Cr2TiC2TxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual toluene;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Cr2TiC2TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) 6 MXene with gradually increased size can be obtained by freeze drying Cr2TiC2TxAnd (3) obtaining the product.
Example 35
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first, 20mL of 6M HCl solution was mixed with 1.28g LiF to generate HF in situ, and 2g of Cr was added2TiAlC2The ceramic powder was slowly added and etched for 42h at 55 ℃ with a stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a multilayer MXene Cr2TiC2Tx；
2) In multiple layers of MXene Cr2TiC2TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Cr2TiC2TxThe volume ratio of the mixed solution of (1): 1, adding xylene to wash (centrifugal washing, 2000 rpm) for at least three times until MXene Cr2TiC2TxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual xylene;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Cr2TiC2TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) 6 MXene Cr with gradually increased size can be obtained by freeze drying2TiC2TxAnd (3) obtaining the product.
Example 36
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first, 10 mL of 6M HCl solution was mixed with 0.66g LiF to generate HF in situ, and 1g of Ti was added3AlCN ceramic powder is slowly added, and etching is carried out for 12 hours at the temperature of 30 ℃ and the stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a plurality of layers of MXene Ti3CNTx；
2) In multiple layers of MXene Ti3CNTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti3CNTxThe volume ratio of the mixed solution of (1): 1 ratio of dichloromethane (centrifugal washing, 4000 rpm) at least three times to MXene Ti3CNTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours at room temperature to remove residual dichloromethane;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti3CNTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Obtaining 6 MXene Ti with gradually enlarged size by freeze drying3CNTxAnd (3) obtaining the product.
Example 37
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first, 10 mL of 6M HCl solution was mixed with 0.66g LiF to generate HF in situ, and 1g of Ti was added3AlCN ceramic powder is slowly added, and etching is carried out for 12 hours at the temperature of 30 ℃ and the stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a plurality of layers of MXene Ti3CNTx；
2) In multiple layers of MXene Ti3CNTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti3CNTxThe volume ratio of the mixed solution of (1): 1 is washed at least three times by adding carbon tetrachloride (centrifugal washing, 4000 rpm) until MXene Ti is obtained3CNTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours at room temperature to remove residual carbon tetrachloride;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti3CNTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Obtaining 6 MXene Ti with gradually enlarged size by freeze drying3CNTxAnd (3) obtaining the product.
Example 38
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first, 10 mL of 6M HCl solution was mixed with 0.66g LiF to generate HF in situ, and 1g of Ti was added3AlCN ceramic powder is slowly added, and etching is carried out for 12 hours at the temperature of 30 ℃ and the stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a plurality of layers of MXene Ti3CNTx；
2) In multiple layers of MXene Ti3CNTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti3CNTxThe volume ratio of the mixed solution of (1): 1 is added with chloroform for washing (centrifugal washing, 4000 rpm) for at least three times until MXene Ti3CNTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours at room temperature to remove residual trichloromethane;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti3CNTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Obtaining 6 MXene Ti with gradually enlarged size by freeze drying3CNTxAnd (3) obtaining the product.
Example 39
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first, 10 mL of 6M HCl solution was mixed with 0.66g LiF to generate HF in situ, and 1g of Ti was added3AlCN ceramic powder is slowly added, and etching is carried out for 12 hours at the temperature of 30 ℃ and the stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a plurality of layers of MXene Ti3CNTx；
2) In multiple layers of MXene Ti3CNTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti3CNTxThe volume ratio of the mixed solution of (1): 1 is washed at least three times by adding dichloroethane (centrifugal washing, 4000 rpm) to MXene Ti3CNTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours at room temperature to remove residual dichloroethane;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti3CNTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Obtaining 6 MXene Ti with gradually enlarged size by freeze drying3CNTxAnd (3) obtaining the product.
Example 40
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first, 10 mL of 6M HCl solution was mixed with 0.66g LiF to generate HF in situ, and 1g of Ti was added3AlCN ceramic powder is slowly added, and etching is carried out for 12 hours at the temperature of 30 ℃ and the stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a plurality of layers of MXene Ti3CNTx；
2) In multiple layers of MXene Ti3CNTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti3CNTxThe volume ratio of the mixed solution of (1): 1, adding methyl ethyl ketone for washing (centrifugal washing, 4000 rpm) for at least three times until MXene Ti3CNTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours at room temperature to remove residual methyl ethyl ketone;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti3CNTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Obtaining 6 MXene Ti with gradually enlarged size by freeze drying3CNTxAnd (3) obtaining the product.
EXAMPLE 41
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first, 10 mL of 6M HCl solution was mixed with 0.66g LiF to generate HF in situ, and 1g of Ti was added3AlCN ceramic powder is slowly added, and etching is carried out for 12 hours at the temperature of 30 ℃ and the stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a plurality of layers of MXene Ti3CNTx；
2) In multiple layers of MXene Ti3CNTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti3CNTxThe volume ratio of the mixed solution of (1): 1 ratio of toluene is added for washing (centrifugal washing, 4000 rpm) at least three times until MXene Ti is obtained3CNTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours at room temperature to remove residual toluene;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti3CNTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Obtaining 6 MXene Ti with gradually enlarged size by freeze drying3CNTxAnd (3) obtaining the product.
Example 42
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first, 10 mL of 6M HCl solution was mixed with 0.66g LiF to generate HF in situ, and 1g of Ti was added3AlCN ceramic powder is slowly added, and etching is carried out for 12 hours at the temperature of 30 ℃ and the stirring speed of 350 rpm. Then centrifugally washing for 4-6 times by using deionized water until the solution is neutral to obtain a plurality of layers of MXene Ti3CNTx；
2) In multiple layers of MXene Ti3CNTxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 3h, and intercalating;
3) in dimethyl sulfoxide and MXene Ti3CNTxThe volume ratio of the mixed solution of (1): 1 ratio of xylene washing (centrifugal washing, 4000 rpm) at least three times to MXene Ti3CNTxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours at room temperature to remove residual xylene;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene Ti3CNTxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) Obtaining 6 MXene Ti with gradually enlarged size by freeze drying3CNTxAnd (3) obtaining the product.
Example 43
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first, 10 mL of 12M HCl solution was mixed with 0.6g LiF to form HF in situ, and 1g of (Nb)0.8Zr0.2)4AlC3Slowly adding ceramic powder, etching at 50 deg.C and stirring speed of 350rpm for 168h, and centrifuging and washing with deionized water for 4-6 times until neutral to obtain multilayer MXene (Nb)0.8Zr0.2)4C3Tx；
2) In multiple layers of MXene (Nb)0.8Zr0.2)4C3TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 1h, and intercalating;
3) in dimethyl sulfoxide and MXene (Nb)0.8Zr0.2)4C3TxThe volume ratio of the mixed solution of (1): 1 ratio, washing with dichloromethane (centrifugal washing, 3000 rpm) at least three times to obtain MXene (Nb)0.8Zr0.2)4C3TxThe dimethyl sulfoxide in the solution is basically removed to be cleanAfter that, vacuum drying is carried out for 2h to remove residual dichloromethane;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene (Nb)0.8Zr0.2)4C3TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) 6 MXene (Nb) with gradually increased size can be obtained by freeze drying0.8Zr0.2)4C3TxAnd (3) obtaining the product.
Example 44
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first, 10 mL of 12M HCl solution was mixed with 0.6g LiF to form HF in situ, and 1g of (Nb)0.8Zr0.2)4AlC3Slowly adding ceramic powder, etching at 50 deg.C and stirring speed of 350rpm for 168h, and centrifuging and washing with deionized water for 4-6 times until neutral to obtain multilayer MXene (Nb)0.8Zr0.2)4C3Tx；
2) In multiple layers of MXene (Nb)0.8Zr0.2)4C3TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 1h, and intercalating;
3) in dimethyl sulfoxide and MXene (Nb)0.8Zr0.2)4C3TxThe volume ratio of the mixed solution of (1): 1 is washed at least three times by adding carbon tetrachloride (centrifugal washing, 3000 rpm) until MXene (Nb)0.8Zr0.2)4C3TxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual carbon tetrachloride;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene (Nb)0.8Zr0.2)4C3TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) 6 MXene (Nb) with gradually increased size can be obtained by freeze drying0.8Zr0.2)4C3TxAnd (3) obtaining the product.
Example 45
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first, 10 mL of 12M HCl solution was mixed with 0.6g LiF to form HF in situ, and 1g of (Nb)0.8Zr0.2)4AlC3Slowly adding ceramic powder, etching at 50 deg.C and stirring speed of 350rpm for 168h, and centrifuging and washing with deionized water for 4-6 times until neutral to obtain multilayer MXene (Nb)0.8Zr0.2)4C3Tx；
2) In multiple layers of MXene (Nb)0.8Zr0.2)4C3TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 1h, and intercalating;
3) in dimethyl sulfoxide and MXene (Nb)0.8Zr0.2)4C3TxThe volume ratio of the mixed solution of (1): 1 ratio, at least three times, to MXene (Nb)0.8Zr0.2)4C3TxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual trichloromethane;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene (Nb)0.8Zr0.2)4C3TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) 6 MXene (Nb) with gradually increased size can be obtained by freeze drying0.8Zr0.2)4C3TxAnd (3) obtaining the product.
Example 46
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) firstly, 10 mL of 12Mixing M HCl solution with 0.6g LiF to generate HF in situ, and mixing 1g (Nb)0.8Zr0.2)4AlC3Slowly adding ceramic powder, etching at 50 deg.C and stirring speed of 350rpm for 168h, and centrifuging and washing with deionized water for 4-6 times until neutral to obtain multilayer MXene (Nb)0.8Zr0.2)4C3Tx；
2) In multiple layers of MXene (Nb)0.8Zr0.2)4C3TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 1h, and intercalating;
3) in dimethyl sulfoxide and MXene (Nb)0.8Zr0.2)4C3TxThe volume ratio of the mixed solution of (1): 1, at least three times, to MXene (Nb)0.8Zr0.2)4C3TxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual dichloroethane;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene (Nb)0.8Zr0.2)4C3TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) 6 MXene (Nb) with gradually increased size can be obtained by freeze drying0.8Zr0.2)4C3TxAnd (3) obtaining the product.
Example 47
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first, 10 mL of 12M HCl solution was mixed with 0.6g LiF to form HF in situ, and 1g of (Nb)0.8Zr0.2)4AlC3Slowly adding ceramic powder, etching at 50 deg.C and stirring speed of 350rpm for 168h, and centrifuging and washing with deionized water for 4-6 times until neutral to obtain multilayer MXene (Nb)0.8Zr0.2)4C3Tx；
2) In multiple layers of MXene (Nb)0.8Zr0.2)4C3TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 1h, and intercalating;
3) in dimethyl sulfoxide and MXene (Nb)0.8Zr0.2)4C3TxThe volume ratio of the mixed solution of (1): 1, adding methyl ethyl ketone for washing (centrifugal washing, 3000 rpm) at least three times to obtain MXene (Nb)0.8Zr0.2)4C3TxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual methyl ethyl ketone;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene (Nb)0.8Zr0.2)4C3TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the obtained precipitate was subjected to the operations 2) to 4) repeatedly for 6 cycles.
6) 6 MXene (Nb) with gradually increased size can be obtained by freeze drying0.8Zr0.2)4C3TxAnd (3) obtaining the product.
Example 48
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first, 10 mL of 12M HCl solution was mixed with 0.6g LiF to form HF in situ, and 1g of (Nb)0.8Zr0.2)4AlC3Slowly adding ceramic powder, etching at 50 deg.C and stirring speed of 350rpm for 168h, and centrifuging and washing with deionized water for 4-6 times until neutral to obtain multilayer MXene (Nb)0.8Zr0.2)4C3Tx；
2) In multiple layers of MXene (Nb)0.8Zr0.2)4C3TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 1h, and intercalating;
3) in dimethyl sulfoxide and MXene (Nb)0.8Zr0.2)4C3TxThe volume ratio of the mixed solution of (1): 1 ratio of toluene addition washing (centrifugal washing, 3)000 rpm) at least three times, to MXene (Nb)0.8Zr0.2)4C3TxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual toluene;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene (Nb)0.8Zr0.2)4C3TxThen centrifuging at 3500rpm for 30min to separate the product;
5) the obtained precipitate was subjected to the operations 2) to 4) repeatedly for 6 cycles.
6) 6 MXene (Nb) with gradually increased size can be obtained by freeze drying0.8Zr0.2)4C3TxAnd (3) obtaining the product.
Example 49
A method for synthesizing and collecting MXene with the assistance of organic solvent comprises the following steps:
1) first, 10 mL of 12M HCl solution was mixed with 0.6g LiF to form HF in situ, and 1g of (Nb)0.8Zr0.2)4AlC3Slowly adding ceramic powder, etching at 50 deg.C and stirring speed of 350rpm for 168h, and centrifuging and washing with deionized water for 4-6 times until neutral to obtain multilayer MXene (Nb)0.8Zr0.2)4C3Tx；
2) In multiple layers of MXene (Nb)0.8Zr0.2)4C3TxAccording to 1 g: adding dimethyl sulfoxide into 20mL of feed ratio, stirring for 1h, and intercalating;
3) in dimethyl sulfoxide and MXene (Nb)0.8Zr0.2)4C3TxThe volume ratio of the mixed solution of (1): 1 ratio, xylene wash (centrifuge wash, 3000 rpm) at least three times to MXene (Nb)0.8Zr0.2)4C3TxAfter dimethyl sulfoxide in the solution is basically removed, vacuum drying is carried out for 2 hours to remove residual xylene;
4) adding a proper amount of deionized water, and performing vortex oscillation to disperse MXene (Nb)0.8Zr0.2)4C3TxThen at 3Centrifuging at 500rpm for 30min to separate the product;
5) the resulting precipitate was repeated 2) to 4), and the cycle was repeated 6 times.
6) 6 MXene (Nb) with gradually increased size can be obtained by freeze drying0.8Zr0.2)4C3TxAnd (3) obtaining the product.