CN111785534A - Method for immobilizing MXene by ionic liquid covalent bonding and product thereof - Google Patents

Method for immobilizing MXene by ionic liquid covalent bonding and product thereof Download PDF

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CN111785534A
CN111785534A CN202010516463.9A CN202010516463A CN111785534A CN 111785534 A CN111785534 A CN 111785534A CN 202010516463 A CN202010516463 A CN 202010516463A CN 111785534 A CN111785534 A CN 111785534A
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mxene
ionic liquid
covalent bonding
metal
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CN111785534B (en
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赵龙
文迪
谢康俊
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Huazhong University of Science and Technology
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
    • H01G11/00Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/84Processes for the manufacture of hybrid or EDL capacitors, or components thereof
    • H01G11/86Processes for the manufacture of hybrid or EDL capacitors, or components thereof specially adapted for electrodes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00Nanotechnology for materials or surface science, e.g. nanocomposites
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y40/00Manufacture or treatment of nanostructures
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B21/00Nitrogen; Compounds thereof
    • C01B21/082Compounds containing nitrogen and non-metals and optionally metals
    • C01B21/0828Carbonitrides or oxycarbonitrides of metals, boron or silicon
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00Carbon; Compounds thereof
    • C01B32/90Carbides
    • C01B32/914Carbides of single elements
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00Carbon; Compounds thereof
    • C01B32/90Carbides
    • C01B32/914Carbides of single elements
    • C01B32/921Titanium carbide
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
    • H01G11/00Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/22Electrodes
    • H01G11/24Electrodes characterised by structural features of the materials making up or comprised in the electrodes, e.g. form, surface area or porosity; characterised by the structural features of powders or particles used therefor
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
    • H01G11/00Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/22Electrodes
    • H01G11/30Electrodes characterised by their material

Abstract

The invention belongs to the field of nano functional materials, and discloses a method for immobilizing MXene by ionic liquid covalent bonding and a product thereof. Adding MXene materials containing-OH, -F, -O end groups into an ionic liquid monomer solution containing unsaturated double bonds, carrying the ionic liquid on the surface of the MXene materials through covalent bonding and immobilization by an ionizing radiation technology, and washing and centrifuging to obtain a series of ionic liquid covalent bonding and immobilization MXene materials containing different structures. The preparation method provided by the invention can be used for reaction at normal temperature, does not need a catalyst, and has the advantages of fast reaction, easiness in control and low energy consumption. The method solves the problem of MXene nanosheet stacking, enriches the types of active sites of the MXene nanosheets or increases the chemical effective active area of the MXene nanosheets. The synthesized MXene composite material maintains the nano structure of the MXene material, has the advantages of MXene and ionic liquid, and has good application prospects in the aspects of energy storage, catalysis, sensing and adsorption.

Description

Method for immobilizing MXene by ionic liquid covalent bonding and product thereof
Technical Field
The invention belongs to the field of nano functional materials, and particularly relates to a method for immobilizing MXene by ionic liquid covalent bonding and a product thereof.
Background
The two-dimensional transition metal carbide and nitride (MXene) is obtained by selectively corroding an A atomic layer of MAX phase in a specific chemical environment, has terminal functional groups of-OH, -O, -H, -F and the like on the surface, has a structure similar to that of graphene, has a large specific surface area, excellent chemical properties, good conductivity and Lewis-acidity, and is widely applied to the aspects of energy storage/conversion, optical/electro-catalysis, chemical sensing, electrostatic shielding and adsorption. However, the MXene lamellar structure is susceptible to re-stacking, resulting in a large loss of active surface area, affecting the diffusion of ions between layers, and thus limiting its application.
Recently, chinese patent CN 109449002 a discloses the direct irradiation of aqueous Ti3C2Tx dispersions with gamma rays or electron beams for surface modification. The modified Ti3C2Tx material has a fold structure and amorphous carbon, and is beneficial to improving the active specific surface area and improving the capacitance performance. Chinese patent CN110760075A discloses a method for preparing Ti by radiation polymerization initiated by gamma rays or electron beams3C2TxComposite double-network hydrogel, wherein Ti3C2TxAs an additive, Ti is imparted with its highly strain-dependent electrical resistance characteristics3C2TxThe composite double-network hydrogel has high-sensitivity strain sensor performance. However, the modification of MXene by radiation technology in these studies is relatively single, and only MXene itself is modified and used as an additive, which cannot satisfy different purposes. The modification of MXene materials by covalent bonding with monomers with specific functions needs to be further investigated.
Ionic Liquids (ILs) are liquid substances which consist of ions only at room temperature and have negligible evaporationVapor pressure, adjustable solubility and high thermal stability. Moreover, the physicochemical properties of the anions and the cations can be modulated by changing the types or the structures of the anions and the cations to obtain the functionalized ionic liquid. The ionic liquid modified MXene material has been reported. The Chinese invention patent CN 108379876A discloses an adsorbent obtained by mixing functionalized ionic liquid and MXene materials by utilizing electrostatic action, and the method has the advantages of long reaction time, weak binding force between the ionic liquid and the MXene and easy loss. Sun Yiming et al (EnergyStorage Science and Technology, 2095-3C2Tx) As an electrode material of a super capacitor. However, this method is complicated in operation and has a long reaction time.
Disclosure of Invention
Aiming at the defects of the prior art, the invention aims to provide a method for immobilizing MXene by ionic liquid covalent bonding and a product thereof, solves the technical problems that MXene materials are easy to re-accumulate and few in active sites, and overcomes the defects of high energy consumption, complex operation and the like of the existing modification method.
In order to achieve the aim, the invention provides a method for immobilizing MXene by ionic liquid covalent bonding, which comprises the following steps
Preparing MXene material nanosheet dispersion liquid;
carrying out ultrasonic treatment and deoxidization sealing on the MXene material nanosheet dispersion liquid, adding an ionic liquid monomer containing unsaturated double bonds for mixing, and carrying out radiation grafting reaction;
and centrifuging and washing a product obtained by the radiation grafting reaction to obtain the ionic liquid covalent bonding immobilized MXene material.
Further, the MXene material nanosheet dispersion is obtained by adding a MAX phase material into a fluorine-containing solution for etching and ultrasonic processing.
Further, the MXene material is MXene, a metal nano material @ MXene composite material or a metal oxide nano material @ MXene composite material.
Further, MXene has a general formula of Mn+1XnTxWherein M is an early transition metal, X is carbon and/or nitrogen, Tx is a surface termination group, and n is 1 or 2 or 3.
Further, the metal nano material comprises one or more of ferromagnetic metal and alloy thereof, gold, silver and copper.
Further, the mass concentration of MXene is 0.5-60 mg/mL, and the addition amount of the metal salt ensures the mass of the provided metal: the ratio of the MXene to the MXene is (1-9) to (1-30).
Furthermore, the ionic liquid is one or more of imidazole salt, pyridine salt, quaternary ammonium salt and quaternary phosphonium salt room-temperature ionic liquid containing unsaturated double bonds.
Further, the concentration of the ionic liquid is 5 wt% -30 wt%, and the solvent is water, methanol, toluene, N-dimethylformamide or an emulsion system.
Furthermore, the volume ratio of the MXene material to the ionic liquid is (1-5): (1-50).
According to another aspect of the invention, the product prepared by the method is provided, and the form of the ionic liquid covalently bonded and immobilized MXene material is a lamellar structure.
Through the technical scheme, compared with the prior art, the invention has the following beneficial effects:
(1) the method for modifying the radiation grafting ionic liquid solves the problem of re-accumulation of the MXene nanosheets, and enriches the types of active sites of the MXene nanosheets or increases the chemical effective active area of the MXene nanosheets. The prepared ionic liquid covalent bonding MXene composite material maintains the nano structure of the MXene material, has the advantages of the ionic liquid and the MXene, and has good application prospects in the aspects of energy storage, catalysis, sensing and adsorption.
(2) Compared with the defects of complex modification operation, difficult control, long reaction time, difficult realization of mass production and the like of the traditional chemical method, the radiation grafting technology related by the invention is a modification method with mild reaction condition, fast reaction, environmental protection, simple and convenient operation and easy control. A series of ionic liquids containing unsaturated double bonds are grafted on an MXene substrate, so that the method has the advantages of low loss of the ionic liquids, no need of adding an initiator or a catalyst in the reaction, high yield and the like; moreover, modified materials with different grafting ratios can be obtained by adjusting the radiation dose and the dose ratio, and the large-scale industrial production of the ionic liquid covalently bonded MXene can be realized.
Drawings
Fig. 1 is a scanning electron microscope spectrogram of an MXene nanosheet provided by an embodiment of the present invention.
Fig. 2 is a thermogravimetric diagram of MXene nanosheets, 10%, 20%, 30% ionic liquid covalently bonded to MXene material provided by an embodiment of the present invention.
Fig. 3 is an infrared diagram of MXene nanosheet, Fe @ MXene material and 10% ionic liquid covalently bonded Fe/MXene material provided by an embodiment of the present invention.
Fig. 4 is a thermogram of MXene nanoplatelets, ionic liquid covalently bonded Fe @ MXene material and 10% ionic liquid covalently bonded Fe @ MXene material according to an embodiment of the present invention.
FIG. 5 is an XRD pattern of an ionic liquid covalently bonded Fe @ MXene material and a 10% ionic liquid covalently bonded Fe @ MXene material according to an embodiment of the invention.
Detailed Description
In order to make the objects, technical solutions and advantages of the present invention more apparent, the present invention is described in further detail below with reference to the accompanying drawings and embodiments. It should be understood that the specific embodiments described herein are merely illustrative of the invention and are not intended to limit the invention. In addition, the technical features involved in the embodiments of the present invention described below may be combined with each other as long as they do not conflict with each other.
The invention provides a preparation method of MXene immobilized by ionic liquid covalent bonding, which comprises the following steps:
step one, preparing MXene nano-sheets: adding MAX phase materials into a fluorine-containing solution for etching and ultrasonic treatment to obtain MXene nanosheet dispersion.
And step two, taking MXene nanosheet dispersion liquid with a certain concentration, ultrasonically dispersing uniformly, introducing inert gas, sealing, and adding an ionic liquid monomer containing unsaturated double bonds to perform radiation grafting reaction with MXene.
And step three, centrifuging and washing the product obtained in the step two to obtain the ionic liquid covalent bonding immobilized MXene material.
The general formula of MXene in the first step is Mn+1XnTx(n-1-3) wherein M is an early transition metal (Sc, Ti, Zr, Hf, V, Nb, Ta, Cr, Mo, etc.), X is carbon and/or nitrogen, and Tx is a surface termination group (e.g., OH, O, or F).
Preferably, MXene is Ti2CTx、Ti3C2Tx、Ti3CNTx、Ta4C3Tx、Nb2CTx、V2CTxOr Nb4C3Tx
In the first step, the MXene nano sheet material is in a sheet structure, and the sheet structure is formed by a single layer or multiple layers of Mn+1XnFormed of, or consisting of, single or multiple layers Mn+1And X. Preferably, the transverse dimension of the lamellar structure is 5 nm-50 mu m, and the thickness of each single sheet is 0.5-100 nm.
In the first step, the MXene material can also be a composite material of a metal nano material @ MXene or a composite material of a metal oxide nano material @ MXene.
Preferably, the metal nanomaterial comprises one or more of ferromagnetic metals and alloys thereof, gold, silver, copper. The metal oxide nano material comprises one or more of ferric oxide, zinc oxide, magnesium oxide, copper oxide, nickel oxide, praseodymium oxide, tin dioxide, silicon dioxide, titanium dioxide, zirconium dioxide, cerium dioxide, aluminum oxide, manganese oxide, zinc ferrite, nickel ferrite and cobalt ferrite.
Preferably, the mass concentration of MXene is 0.5-60 mg/mL, and the addition amount of the metal salt ensures the mass of the metal provided by the MXene: the ratio of the MXene to the MXene is (1-9) to (1-30).
And the kind of the ionic liquid in the second step is one or more of imidazole salt, pyridine salt, quaternary ammonium salt and quaternary phosphonium salt room-temperature ionic liquids containing unsaturated double bonds.
Preferably, the ionic liquid species selected are vinyl and allyl with cations containing unsaturated double bonds and the anion X is Cl, Br, I, BF4,PF6And NTF2One or more of the alkenyl functional ionic liquid(s).
Preferably, the concentration of the ionic liquid in the second step is 5 wt% -30 wt%, and the solvent is water, methanol, toluene, N-dimethylformamide or an emulsion system.
The ratio of the MXene material to the ionic liquid in the second step is (1-5) to (1-50).
Preferably, the radiation grafting dose in the second step is 5 kGy-300 kGy, and the grafting rate of the graft polymerization is 3% -100%.
In addition, according to the material obtained by the preparation method, the ionic liquid is immobilized on the MXene material by the radiation grafting technology, the grafting rate is 3% -100%, and the obtained ionic liquid is in a lamellar structure in a covalent bonding mode; the transverse size of the lamellar structure is 5 nm-200 mu m, and the thickness of each single piece is 0.5-1 mu m.
Example one
The preparation method of the ionic liquid covalent immobilized MXene comprises the following steps:
step one, preparing MXene nano-sheets: adding 1g of LiF into a 50mL polytetrafluoroethylene container, adding 20mL of 9MHCl, stirring at room temperature for 30min to obtain a colorless and transparent solution, weighing 1g of Ti3AlC2, slowly adding the solution in batches, stirring at 35 ℃ for 48h, centrifuging the obtained reaction solution (3500rpm, 5min), washing until the pH value of the supernatant poured out after centrifugation is more than 5, preferably 5-7, and taking the precipitate. Adding 80mL of H2O, performing ice bath ultrasonic treatment (600W, 20min), collecting the upper-layer black Zongzi color liquid, namely the less-layer Ti3C2Tx dispersion liquid, repeatedly adding water into the multilayer Ti3C2Tx to obtain more less-layer Ti3C2Tx, shaking up the ultrasonic treatment to collect the upper-layer black Zongzi color liquid, preferably, repeating for 3-5 times, and combining the collected black Zongzi color liquidThe rice dumpling is colored liquid. Obtaining Ti with a concentration of about 7.5mg/mL in a single layer or in a few layers3C2TxAnd (3) dispersing the mixture.
Step two, preparing an ionic liquid covalent immobilized MXene material: 5mL of the Ti layer of small thickness obtained in the first step3C2TxThe suspension is put into a polyethylene bag and spread flat, and is vacuumized and sealed, 5mL of 10 wt% 1-vinyl ethyl imidazole chloride ionic liquid solution which is aerated with nitrogen and deoxidized is injected and sealed, radiation grafting is carried out under accelerator beams, the radiation dose rate is 20kGy/pass, and the absorption dose is 160 kGy.
Step three: and (5) washing the product obtained in the step two with ethanol and water or performing soxhlet extraction with toluene, and then centrifuging and freezing to obtain the needed MXene immobilized by the ionic liquid.
SEM test of the product of the first step in example one, as shown in FIG. 1, is a SEM image of Ti3C2Tx with a single layer or few layers, and it can be seen that Ti3C2Tx is in the form of thin yarn, indicating that MXene was successfully exfoliated.
Example two
An improvement was made over the process provided in example one, except that the ionic liquid concentration was 20 wt%.
EXAMPLE III
An improvement was made over the process provided in example one, except that the ionic liquid concentration was 30 wt%.
The products from examples one to three were subjected to thermogravimetric testing. As shown in fig. 2, a thermogravimetric analysis diagram of MXene, 10%, 20%, 30% ionic liquid covalently bonded immobilized MXene is shown, the grafting rate of 10% ionic liquid covalently bonded immobilized MXene is about 22%, and the grafting rate of 20% ionic liquid and 30% ionic liquid covalently bonded immobilized MXene is about 50%. The grafting rate is gradually increased along with the increase of the ion concentration, and the grafting rate is kept unchanged after the MXene surface is increased to a certain concentration due to the limited surface area of the MXene surface.
Example four
A method for preparing an ionic liquid covalent immobilization-magnetic metal/MXene composite material comprises the following steps:
s1, preparation of MXene nanosheets: the same procedure as in example one.
S2, preparation of MXene nano-sheets loaded with magnetic Fe nano-particles: 1g of FeSO is taken47H2O in a beaker, 20mL of water are added, after complete dissolution, the flask is transferred to a three-neck flask, and 20mL of ultrasonically dispersed, less-layered Ti are added3C2TxSuspending the mixture in a sealed environment at room temperature under N2Protecting and stirring for 24h, adding 10mL of 2mol/L sodium borohydride solution by using an injector, reacting for 30min, and quickly filtering out the reaction solution. Washing with anhydrous ethanol and oxygen-free deionized water, centrifuging (10000W, 10min) for multiple times, preferably 3-8 times, and drying in vacuum drying oven to obtain black powder as Fe/Ti3C2And (c) a complex.
S3, ionic liquid covalent immobilization Fe/Ti3C2Preparation of the complex:
s31, taking 2mg of the few-layer Ti obtained in the step 23C2TxPlacing the suspension into a polyethylene bag, paving the polyethylene bag, vacuumizing and sealing the polyethylene bag, injecting 5mL of 10 wt% 1-vinyl ethyl imidazole chloride ionic liquid solution which is filled with nitrogen and deoxidized, sealing the polyethylene bag, and carrying out radiation grafting under an accelerator beam, wherein the radiation dose rate is 20kGy/pass, and the absorption dose is 160 kGy;
s32, washing the product obtained in the step S31 with ethanol and water or performing soxhlet extraction with toluene, and centrifuging to obtain the required ionic liquid covalently immobilized Fe/Ti3C2A composite material.
The product from example four was tested by infrared. As shown in FIG. 3, an infrared image of MXene, MXene @ Fe and 10% ionic liquid covalently bonded immobilized MXene @ Fe is shown, and as can be seen from the figure, MXene has a distinct infrared characteristic peak, and 10% ionic liquid covalently bonded immobilized MXene @ Fe also appears at 1228cm-1、1560cm-1C-N, C ═ N peak of imidazole of (2), 1506cm-1C ═ C, indicating that the vinylimidazole ionic liquid was successfully immobilized on MXene @ Fe.
The product from example four was subjected to thermogravimetric testing. Referring to FIG. 4, a thermogravimetric analysis of covalent bonding of MXene, MXene @ Fe and 10% ionic liquid to immobilized MXene @ Fe is shown, and the grafting rate of the ionic liquid is 45% calculated from thermogravimetric weight data.
XRD testing was performed on the product obtained in example four. Referring to FIG. 5, an XRD pattern of MXene @ Fe and 10% ionic liquid covalently bonded to immobilized MXene @ Fe is shown, and it can be seen that: the XRD peak of the MXene @ Fe composite material has the reported characteristic peak of few or single MXene, the characteristic peak of Fe is displayed at the 2 theta-44 degrees, and the characteristic peak of Fe in MXene @ Fe is not obvious when the 10% ionic liquid is covalently bonded and immobilized, so that the Fe content is reduced and the detection is difficult. And the change of XRD spectrogram before and after grafting is small, which shows that the crystallinity and the structure change of MXene are small in the radiation grafting process.
Comparative example 1
Different from the method in the embodiment, the irradiation dose is 20kGy, the grafting rate of the ionic liquid is very low, and the requirement of MXene material modification cannot be met.
It will be understood by those skilled in the art that the foregoing is only a preferred embodiment of the present invention, and is not intended to limit the invention, and that any modification, equivalent replacement, or improvement made within the spirit and principle of the present invention should be included in the scope of the present invention.

Claims (10)

1. The method for immobilizing MXene by ionic liquid covalent bonding is characterized by comprising the following steps
Preparing MXene material nanosheet dispersion liquid;
carrying out ultrasonic treatment and deoxidization sealing on the MXene material nanosheet dispersion liquid, adding an ionic liquid monomer containing unsaturated double bonds for mixing, and carrying out radiation grafting reaction;
and centrifuging and washing a product obtained by the radiation grafting reaction to obtain the ionic liquid covalent bonding immobilized MXene material.
2. The method of claim 1, wherein the MXene material nanoplatelet dispersion is obtained by adding MAX phase material to a fluorine-containing solution for etching and sonication.
3. The method of claim 2, wherein the MXene material is MXene, a metal nanomaterial @ MXene composite, or a metal oxide nanomaterial @ MXene composite.
4. The method of claim 3, wherein the MXene has the formula Mn+1XnTxWherein M is an early transition metal, X is carbon and/or nitrogen, Tx is a surface termination group, and n is 1 or 2 or 3.
5. The method of claim 3, wherein the metallic nanomaterial comprises one or more of a ferromagnetic metal and alloys thereof, gold, silver, and copper.
6. The method according to claim 5, wherein the MXene has a mass concentration of 0.5-60 mg/mL, and the metal salt is added in an amount that ensures the mass of the metal provided by the MXene: the ratio of the MXene to the MXene is (1-9) to (1-30).
7. The method according to claim 1, wherein the ionic liquid is one or more of imidazole salts, pyridine salts, quaternary ammonium salts and quaternary phosphonium salts room-temperature ionic liquids containing unsaturated double bonds.
8. The method of claim 1, wherein the ionic liquid has a concentration of 5 wt% to 30 wt% and the solvent is water, methanol, toluene, N-dimethylformamide, or an emulsion system.
9. The method according to claim 1, wherein the ratio of the MXene material to the ionic liquid by volume is (1-5): (1-50).
10. The product prepared by the method according to any one of claims 1 to 9, wherein the ionic liquid covalently bonded supported MXene material is in a lamellar structure.
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