CN102701187A - Preparation method of graphene and graphene prepared by same - Google Patents
Preparation method of graphene and graphene prepared by same Download PDFInfo
- Publication number
- CN102701187A CN102701187A CN2011101208681A CN201110120868A CN102701187A CN 102701187 A CN102701187 A CN 102701187A CN 2011101208681 A CN2011101208681 A CN 2011101208681A CN 201110120868 A CN201110120868 A CN 201110120868A CN 102701187 A CN102701187 A CN 102701187A
- Authority
- CN
- China
- Prior art keywords
- graphene
- compound
- graphite
- preparation
- graphite layers
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Images
Landscapes
- Carbon And Carbon Compounds (AREA)
Abstract
The invention relates to a preparation method of graphene and graphene prepared by the method, and is characterized in that the method adopts graphite as a raw material; a graphite intercalation compound is prepared by intercalating metal between graphite layers; and then graphene is prepared by peeling the graphite intercalation compound. The graphene prepared by the method has a length and a width of 5-15000 nm, and a thickness of 0.3-15 nm. The advantages of the invention are that: the raw material source is wide; the cost is low; the preparation method is simple; the product performance is stable and controllable; and the method is suitable for industrial production.
Description
[technical field]
The present invention relates to the Graphene technical field, specifically, the present invention relates to a kind of preparation method of graphene and the Graphene that uses this method preparation.
[background technology]
Graphene (Graphene) is a kind ofly after soccerballene, carbon nanotube to be the allotropic substance of the human carbon of being familiar with recently.Graphene is that a kind of carbon atom is with sp
2Hybridized orbital Cheng Jian, the carbon material of the individual layer bi-dimensional cellular shape crystalline network that forms with six-membered ring structure.This particular structure of Graphene has been brought a series of novelties, special nature to it; Such as water white transparency (absorb light intensity is merely 2.3%), electric conductivity high (single-layer graphene electric conductivity and copper are close), (tensile strength can reach 50～200GPa to the mechanical property excellence; Young's modulus can reach 1TPa, and the tensile strength of single-layer graphene is 100 times of condition of equivalent thickness steel disc).Above characteristic makes Graphene have broad application prospects in many new forms of energy, field of new such as touch-screen, solar cell, aerospace materials.Therefore the preparation and the property research thereof of Graphene have become the focus in the nano science research in recent years.
Preparation method of graphene is concluded, and mainly contains micromechanics and peels off method, chemical Vapor deposition process (CVD), reduction-oxidation graphite method etc.
Wherein, to peel off method be successfully to prepare the method for Graphene the earliest to micromechanics.This method is to utilize tearing repeatedly to take off and from highly oriented pyrolytic graphite, separating (K.S.Novoselov to graphene film of adhesive tape; Et al.Science, 306,666 (2004)); Can prepare high-quality Graphene though adopt this method; But this method expensive raw materials, the preparation process is consuming time serious, can't realize scale operation.
Chemical Vapor deposition process is under pyrocarbon hydrogen compound (like methane) atmosphere, thereby makes the carbon laydown in the hydrocarbon polymer to the transition metal substrate, make Graphene (Jessica Campos-Delgado, et al.Nano Letters, 8,9 (2008)).This method can make larger-size grapheme material, and still, the manufacturing cost Graphene product number of plies too high and gained is difficult to control, and then has limited the application of product.
Reduction-oxidation graphite method is the main method of a large amount of at present preparation Graphenes.This method obtains graphene oxide through peeling off then earlier with graphite oxidation, at last the graphene oxide that obtains is obtained Graphene through reduction.Though this method can prepare Graphene (Vincent C., et al.Nat Nanotech, 4 in a large number; 25 (2008)), still, because this method relates to oxidation, reduction process; Final gained Graphene still can contain the partially oxidation group, and these oxide groups have destroyed the sp of Graphene
2Structure can cause the performance of Graphene, particularly conductivity to have a strong impact on.
For solving the problem that above-mentioned preparation method exists, the related patent U.S. Patent No. of present domestic existence partly is exemplified below.
One Chinese patent application number: 200910084879.1, patent name: preparation method of graphene.This inventive method is to react in ionic liquid through carbon nanotube and oxygenant to make Graphene.This method steps is simple, and easy handling is fit to large-scale commercial prodn.
One Chinese patent application number: 200880112966.7, patent name: a kind of preparation method of two-dimension single layer plumbago alkene.This invention prepares the catalyzer that single-layer graphene is used earlier, under inert gas environment, in the container that catalyzer is housed, feeds the carbon source Pintsch process afterwards and makes two-dimension single layer plumbago alkene.
In sum, the technology for preparing Graphene at present can't satisfy industriallization basic demands such as the preparation method is simple, with low cost, product performance stable and controllable, and this has just limited Graphene in wider, the more application of wide field greatly.
[summary of the invention]
The objective of the invention is to overcome the deficiency of prior art, a kind of preparation method of graphene and the Graphene that uses this method preparation are provided.
The objective of the invention is to realize through following technical scheme:
A kind of preparation method of graphene is a raw material with graphite, makes compound between graphite layers through inserting metal in graphite layers, peels off said compound between graphite layers then and makes Graphene.
The selection of described graphite does not have particular restriction, can comprise natural graphite, synthetic graphite, specifically, comprises natural flake graphite, highly oriented pyrolytic graphite or special spherical graphite etc.Therefore can reach raw material sources purpose extensive, with low cost.
Described insertion metal be in basic metal, earth alkali metal, the rare earth metal a kind of, two or more:
Described basic metal is lithium (Li), sodium (Na), potassium (K), rubidium (Ru), caesium (Cs), francium (Fr);
Described earth alkali metal is beryllium (Be), magnesium (Mg), calcium (Ca), strontium (Sr), barium (Ba), radium (Ra);
Described rare earth metal is lanthanum (La), cerium (Ce), praseodymium (Pr), neodymium (Nd), promethium (Pm), samarium (Sm), europium (Eu), gadolinium (Gd), terbium (Tb), dysprosium (Dy), holmium (Ho), erbium (Er), thulium (Tm), ytterbium (Yb), lutetium (Lu), scandium (Sc), yttrium (Y);
Also can be to be selected from the aforementioned metal two or more, as: lithium (Li)/calcium (Ca), potassium (K)/magnesium (Mg), potassium (K)/scandium (Sc), magnesium (Mg)/calcium (Ca), lithium (Li)/magnesium (Mg)/lanthanum (La) etc.
Insert metal with in basic metal, the earth alkali metal a kind of, two or more serve as preferably, comparatively preferably basic metal, more preferably lithium (Li), potassium (K), rubidium (Ru), caesium (Cs), most preferably lithium (Li).
The preparation method of described compound between graphite layers is selected from a kind of, two or more the combination in the following method: solid phase pressurization, scorification, two warm area vapor transportation methods, liquid phase interpolation, molten salt electrolysis of metals method, battery charging and discharging method.
Wherein, described solid phase pressurization: metal-powder is mixed back reaction under pressurized conditions generate compound between graphite layers with graphite matrix, use this method key to be to have only when the vp of metal surpasses a certain threshold value, insertion reaction just can carry out.Be prone to cause metal and graphite to generate the side reaction of carbide but temperature is too high, so temperature of reaction must be controlled within the specific limits, for needs very high-temperature the metal of insertion reaction could take place, needs pressurize and reduce temperature of reaction.
Described scorification is for directly mixing graphite with metal-powder; Make compound between graphite layers with single thermal source reacting by heating, this method speed of response is fast, and reactive system and process are simple; Be suitable for a large amount of synthesizing, but the reactant that is attached to after the reaction on the compound between graphite layers is difficult to remove.
Described two warm area vapor transportation methods will be for being inserted into material and graphite is respectively charged into the heat-resistant glass tube both sides, and steam and graphite that the inset heating evaporation is produced react.The temperature of inserting material one side in the experiment will be higher than the temperature of graphite one side, is beneficial to insert material and forms steam, prevents that simultaneously the compound between graphite layers that generates from decomposition reaction taking place when temperature is too high.The advantage of this method is to be easy to separated product and reactant after reaction finishes, and shortcoming is that reaction unit is complicated, be difficult to carry out synthesize in a large number, and long reaction time, temperature is high, needs operation under vacuum condition.
The insertion metal that described liquid phase interpolation will be in a liquid state mixes with graphite, reacts and generates compound between graphite layers, and temperature, the stage structure of time to product have very big influence in the reaction.This method equipment is simple, and speed of response is fast, be suitable for a large amount of synthesizing, but because requirement must be with metal melting, temperature is big to the melting point metal dependency in the actually operating.
Described molten salt electrolysis of metals method is an ionogen to insert metal melting salt, is that electrode forms chemical system with graphite, is inserted into graphite as anode, prepares compound between graphite layers through the control of regulating current potential, electric weight.This method synthesis device is simple, and resultant quantity is big, and weak point is that the stability of synthetic product is than additive method difference.
Described battery charging and discharging method can know from name and specifically promptly be divided into two kinds, and a kind of is the battery discharge method, and another kind is the battery charge method.Wherein said battery discharge method is to be anodal with graphite, and metal is a negative pole, adds electrolytic solution and forms battery system.Move according to preset discharge step, metal is inserted into forms compound between graphite layers in the graphite;
Wherein said battery charge method is with agent structure in the process of charging not or rare variation, and the metal that does not react with electrolytic solution is intercalation compound, and graphite is negative pole for anodal, adds electrolytic solution and forms battery system.Move according to the preset charged step, metal is inserted into forms compound between graphite layers in the graphite.
This method technology is simple, and reaction conditions is gentle, and can discharge and recharge end condition through preset, obtains the controlled compound between graphite layers of exponent number, is suitable for suitability for industrialized production.
In a preferred embodiment; The method for preparing compound between graphite layers serves as preferred with solid phase pressurization, scorification, liquid phase interpolation, molten salt electrolysis of metals method and battery charging and discharging method; More preferably electrolytic process and battery charging and discharging method, most preferably battery charging and discharging method.
The described method of peeling off compound between graphite layers is selected from a kind of, two or more the combination in the following method: mechanically peel, stripper are peeled off, electrolytic stripping.
Described mechanically peel makes its bending, depression for compound between graphite layers used, the power of swiping, being pressed into or fracture, thus separate the method for Graphene.The instance of mechanically peel can be to utilize adhesive tape to tear repeatedly to take off compound between graphite layers, makes its attenuation, thereby obtains Graphene.Also can be the compound between graphite layers that utilizes the needleless pointed probe scraping of AFM (AFM) fixing, obtain the thin slice that scrapes and continue abovementioned steps, finally obtain Graphene.Also can be to utilize ball mill that the compound between graphite layers powder that is scattered in the organic solvent is carried out ball milling, thereby obtain Graphene.Use mechanically peel can on the gained Graphene, not introduce heteroatoms, but gained Graphene out-of-shape, and the preparation process is consuming time longer.
It is ionogen that described electrolytic stripping inserts metal melting salt; With graphite is that electrode forms chemical system; Compound between graphite layers makes Graphene as anode thereby through the control of regulating current potential, electric weight the metal continuation insertion compound between graphite layers interlayer of electrolysis generation is peeled off.Use the electrolytic stripping can the mass preparation Graphene, but can leave impurity, for example metal-salt on the gained Graphene.And entire reaction course needs higher temperature, reaction environment is required comparatively harsh.
Described stripper is peeled off and can be utilized two kinds of strippers to peel off: the one, utilize can with the stripper of compound between graphite layers reaction; The gas or the bulking effect that discharge through reaction further enlarge the graphite layers distance; Make graphite flake layer mutually away from obtaining Graphene to breaking away from the constraint of Van der Waals force to each other, finally peeling off; The 2nd, adopt the surface energy stripper close with graphite; Because can reduce the entropy of mixing of stripper and graphite under the close situation of surface energy; Be similar to " similar mixing " principle; So just can let stripper be inserted in the compound between graphite layers, continuing increases the graphite layers distance, obtains Graphene thereby peel off compound between graphite layers.The surface tension of selected stripper needs at 10-70mJ/m
2, more preferably at 20-50mJ/m
2Scope in; Above-mentioned surface tension numerical value all is at 20 ℃ of following sessile drop method test gained.Use the stripper strip operation simple, the stripper wide material sources, the chemical reagent for often having can not introduced heteroatoms on prepared Graphene mostly.
Stripping means most preferably stripper is peeled off.
Described stripper be selected from inorganic liquid and the organic liquid a kind of, two or more.
Described inorganic liquid is selected from water, inorganic acid aqueous solution, water phase surfactant mixture.
The aqueous solution that described inorganic aqueous acid instance is a hydrogenchloride, dilute sulphuric acid, rare nitric acid etc.
Described tensio-active agent instance is polyoxyethylene stearic acid ester (Brij 76); Cetyl trimethylammonium bromide (CTAB); TTAB (TTAB); 1-pyridine acid (PBA); Sodium lauryl sulphate (SDS); X 2073 (SDBS); Lithium dodecyl sulfate (LDS); Sodium cholic acid (SC); Sodium desoxycholate (DOC); Cow-bezoar Sodium desoxycholate (TDOC); Sodium (CHAPS) in 3-[3-(courage amido propyl) dimethylamino] propanesulfonic acid; Lewatit (PSS); Vinylpyrrolidone polymer (PVP); Dodecyl-β-D-maltoside (DBDM); Nonoxynolum (IGEPAL CO-890); Octadecanoic acid ester of polyethylene glycol (Tween 80) etc.
Described organic liquid is selected from alcohol, ketone, ester, amine, sulfone, chlorobenzene, organic acid, ionic liquid.
Wherein said alcohol is the alcohol that contains 1-6 carbon atom.Instance can be methyl alcohol, ethanol, terepthaloyl moietie, 1-propyl alcohol, 2-propyl alcohol, 1,2-Ucar 35,1, ammediol, USP Kosher, 1-butanols, 1-amylalcohol, 1-hexanol etc.;
Wherein said acid is the acid that fowl has 1-6 carbon atom.Instance can be formic acid, acetate, oxalic acid, 1-propionic acid, 2-propionic acid, 1,2-propanedioic acid, 1,3-propanedioic acid, the third three acid, 1-butyric acid, 1-valeric acid, 1-caproic acid etc.;
The instance of wherein said ketone can be acetone, 1-Methyl-2-Pyrrolidone, N-vinyl pyrrolidone, octylpyrrolidone, dodecyl pyrrolidone, 1,3-dimethyl--2-imidazolone etc.;
The instance of wherein said ester can be gamma-butyrolactone, peruscabin etc.;
The instance of wherein said amine can be N, N, accelerine, N, dinethylformamide etc.;
The instance of wherein said sulfone can be a DMSO 99.8MIN. etc.;
The instance of wherein said chlorobenzene can be an orthodichlorobenzene etc.;
Wherein said ion liquid instance can be [Bmim] [BF
4], [Bmim] [Tf
2N], [C
4Mim] [PF
6], [C
8Mim] [PF
6], [C
4Mim] Cl, [C
8Mim] Cl etc.
Also can be selected from the mixture of aforesaid two or more composition of liquid, as: water/methyl alcohol, water/ethanol, water/formic acid, ethanol/acetate, water/ethanol/acetate, N-Methyl pyrrolidone/water, [BMIm] [BF
4]/water, [C
4Mim] [PF
6]/N etc.
The length and the width of the Graphene that makes according to method of the present invention are 5～15000nm, and thickness is 0.3～15nm.The thickness of known single-layer graphene is about 0.335nm, so the thickness of Graphene can not be lower than 0.3nm.Because the thickness of Graphene of the present invention is to be recorded by AFM (AFM); But the interaction between AFM probe and substrate and the Graphene can bring measuring error; Therefore the Graphene thickness that records of AFM is generally than about the big 0.4～0.5nm of actual value, and specifically for instance, the single-layer graphene thickness that AFM records is about 0.8nm; The thickness of double-layer graphite alkene is about 1.1nm, and three layer graphene thickness are about 1.5nm.Based on this reason, after state the thickness of listed Graphene among the embodiment owing to all be that employing AFM records, so numerical value is all greater than 0.8.Gained Graphene thickness is at 0.3～15nm among the present invention, and the number of plies is between about 1～45 layer.
The productive rate of Graphene is the ratio of quality with the raw material graphite quality of obtained Graphene.The quality of the Graphene directly final solid graphite alkene of weighing obtains, and also can derive from the concentration of Graphene in the Graphene dispersion liquid.In the Graphene dispersion liquid concentration of Graphene be utilize the absorbancy measure the Graphene dispersion liquid (testing tool as: 722N visible spectrophotometer (Shanghai Precision Scientific Apparatus Co., Ltd's manufacturing)), follow that Law of Lambert-Beer calculates.
The structural information of compound between graphite layers X ray diffracting spectrum capable of using (XRD) measures that (testing tool is like D/MAX 2550 VB/PC (Japanese Rigaku manufactured), target source: the copper target).
The thickness number of plies of said Graphene and length and width size atomic force microscope images capable of using (AFM) are confirmed (testing tool as: NanoScope IIIa MultiMode AFM (U.S. Veeco manufactured), operator scheme: rap pattern).
The length and width size of said Graphene also can use sem (SEM) confirm (testing tool as: SEM (JSM-6360LV) (Japanese JEOL manufactured)).
Strength ratio (the I at D peak and G peak among the defect level of Graphene Raman spectrum capable of using (Raman) figure
D/ I
G) value confirms I
D/ I
GBe worth greatly more, Graphene contained defective is more, and (testing tool is like inVia+Reflex (Britain Renishaw manufactured), laser wavelength: 514nm).
Compared with prior art, positively effect of the present invention is:
(1) raw material sources are extensive, with low cost, and various types of graphite all can be used for preparing Graphene, and used stripper is also mostly to be chemical reagent commonly used; Conveniently be easy to get; Mostly used metal is common metal, particularly lithium, and its reactive behavior is moderate; The success that can guarantee stripping process is carried out, also can be as easy fire that causes of too active metal such as sodium, potassium;
(2) easy, the product performance stable and controllable of preparation method is fit to suitability for industrialized production;
Need Graphene to contain more defective when (3) being used for support of the catalyst and electrode materials, the Graphene of the inventive method preparation itself has more defective, need not further processing, promptly can be used as support of the catalyst or electrode materials.
[description of drawings]
Fig. 1 prepares the method process flow diagram of Graphene for the present invention.
Fig. 2 makes the lithium-compound between graphite layers of single order and X-ray diffraction (XRD) figure of raw material graphite according to embodiment 1, and wherein a is meant compound between graphite layers, and b is meant graphite.
Fig. 3 is that Graphene according to embodiment 1 preparation is at Si0
2AFM on the/Si substrate (AFM) Fig. 5 .00 * 5.00 μ m sizes (a), 1.95 * 1.95 μ m sizes (b) and altitude profile figure (c).
Fig. 4 is the Raman spectrogram according to the Graphene of embodiment 1 preparation.
Fig. 5 is sem (SEM) figure according to the Graphene of embodiment 3 preparations.
[embodiment]
The embodiment of a kind of preparation method of graphene of the present invention below is provided.
Embodiment 1
The battery discharge legal system is equipped with compound between graphite layers
With special spherical graphite SSG (active material) (deriving from Loudi, Hunan brightness space Science and Technology Ltd.), acetylene black (static eliminator; About 10nm), pvdf PVDF (sticker) presses 8: 1: 1 mixed of mass ratio particle diameter:; Adding 1-Methyl-2-Pyrrolidone (NMP) makes PVDF concentration in 0.005～0.03g/ml scope; Stir the furnishing pasty slurry.It is evenly overlayed on the Copper Foil shop; After treating that solvent evaporates is studied carefully entirely; Utilize punch tool to make circular Graphite Electrodes sheet, after 12 hours, select for use metal lithium sheet 80 ℃ of following vacuum-dryings the Graphite Electrodes sheet that makes as GND; Graphite Electrodes is as anode; With lithium hexafluoro phosphate be dissolved in volume ratio be solution in 1: 1: 1 EC/EMC/DMC (NSC 11801/Methyl ethyl carbonate/methylcarbonate) ternary mixed solvent as electrolytic solution, barrier film adopts polypropylene porous film, water, oxygen level less than the glove box of 1ppm in assembled battery.
(testing tool is like: BTS high accuracy battery detection system (the new Weir Electronics Co., Ltd. of China makes) then the battery of assembling to be carried out impulsive discharge; Model: CT-3008W-5V10mA-S1); After being provided with according to parameter given below; Can carry out impulsive discharge: carried out constant-current discharge 5 minutes with the discharge rate of 0.05C in each circulation, left standstill 12 minutes, successively circulation.Pulse discharge time is 7 days, stops discharge then, in water, the glove box of oxygen level less than 1ppm, disassembles battery, takes out the single order lithium-compound between graphite layers of negative pole.After treating the electrolytic solution volatilization; Lithium-compound between graphite layers scraped from the copper sheet gently leave; Place in the agate mortar and grind to form uniform powder; Pour into rapidly the deionized water after in glove box, taking out powdered lithium-compound between graphite layers, deionized water described herein is as stripper, and the metallic lithium in lithium-compound between graphite layers is peeled off and made Graphene.
Utilize spectrophotometer to record the concentration of gained Graphene aqueous dispersions, thus the output of the Graphene that obtains making, and then obtain productive rate.Adopting the Graphene productive rate of preceding method gained present embodiment is 0.56%.
Fig. 2 is the single order compound between graphite layers of embodiment 1 gained lithium and the XRD figure of raw material graphite.Can find out: after graphite layers is inserted metallic lithium, originally disappeared at 26.6 ° of graphite characteristic peaks of locating, replacing is a tangible spike near 24 °, to have occurred.This phenomenon has proved the formation of single order lithium-compound between graphite layers.
Fig. 3 schemes for the AFM that embodiment 1 makes Graphene, and Graphene height that figure (c) is corresponding is 0.8nm, is individual layer.Graphene thickness is between 0.8～7nm, and the number of plies is between about 1～20 layer.Length and width are all between 100nm～5000nm.
Fig. 4 has provided the Raman spectrogram (X-coordinate is a wave number, and ordinate zou is an intensity) of the Graphene of embodiment 1 preparation, can find out the existence of graphite-structure in the G peak explanation Graphene, the existence of defective in the D peak explanation Graphene.The strength ratio I at D peak and G peak
D/ I
GValue is 0.69.
Embodiment 2
The battery discharge legal system is equipped with compound between graphite layers
Except pulse discharge time is 3 beyond the highest heavens, all the other operations are identical with embodiment 1, thereby obtain second order lithium-compound between graphite layers.Final gained Graphene productive rate is 0.59%, gained Graphene thickness between 2.1～9.2, promptly the number of plies between about 5～26 layers, length and width all between 100～6300nm, the strength ratio I at D peak and G peak in the Raman spectrum
D/ I
GValue is 0.68.
Embodiment 3
The battery discharge legal system is equipped with compound between graphite layers
Except pulse discharge time is 2 beyond the highest heavens, all the other operations are identical with embodiment 1, thereby obtain three rank lithium-compound between graphite layers.Final gained Graphene productive rate is 0.45%, gained Graphene thickness between 4.5～11.3, promptly the number of plies between about 12～32 layers, length and width all between 130～7000nm, the strength ratio I at D peak and G peak in the Raman spectrum
D/ I
GValue is 0.67.
Embodiment 4
The battery discharge legal system is equipped with compound between graphite layers
Except pulse discharge time is 32 hours, all the other operations are identical with embodiment 1, thereby obtain quadravalence lithium-compound between graphite layers.Final gained Graphene productive rate is 0.32%, gained Graphene thickness between 6.5～14.4, promptly the number of plies between about 18～42 layers, length and width all between 130～6800nm, the strength ratio I at D peak and G peak in the Raman spectrum
D/ I
GValue is 0.66.
Embodiment 5
The battery discharge legal system is equipped with compound between graphite layers
The battery positive and negative polarities of the assembling described in the embodiment 1 are linked to each other, carried out short circuit dischange 48 hours, all the other operations are identical with embodiment 1.Final gained Graphene productive rate is 0.62%, gained Graphene thickness between 1.5～8.2, promptly the number of plies between about 3～24 layers, length and width all between 50～6500nm, the strength ratio I at D peak and G peak in the Raman spectrum
D/ I
GValue is 0.71.
Embodiment 6
The battery charge legal system is equipped with compound between graphite layers.
With cobalt acid lithium (active material (Beijing Zhongxinguoan Mengguli Electric Source Technology Co., Ltd)), acetylene black (static eliminator; About 10nm), pvdf PVDF (sticker) presses 90: 5: 5 mixed of mass ratio particle diameter:; Adding 1-Methyl-2-Pyrrolidone (NMP) makes pvdf PVDF concentration in 0.005～0.03g/ml scope; Stir the furnishing pasty slurry.It is evenly overlayed on the aluminium foil shop; After treating that solvent evaporates fully; Utilize punch tool to make the positive electrical pole piece; After 12 hours, select for use natural graphite (particle diameter 20～30 μ m) as GND 120 ℃ of following vacuum-dryings the positive electrical pole piece that makes, it is that solution in 1: 1: 1 EC/EMC/DMC (NSC 11801/Methyl ethyl carbonate/methylcarbonate) ternary mixed solvent is as electrolytic solution that lithium hexafluoro phosphate is dissolved in volume ratio; Barrier film adopts polypropylene porous film, water, oxygen level less than the glove box of 1ppm in assembled battery.
Then the battery of assembling is carried out constant current charge to cell voltage with the charge rate of 0.2C and rise to 4.2V.Carry out constant voltage charge to charge rate afterwards and reduce to 0.02C; After shelving 30min; Again battery is carried out constant current charge with the charge rate of 0.2C and be charged to 4.35V earlier; Constant voltage charge to charge rate is reduced to 0.02C (testing tool is like: BTS high accuracy battery detection system (the new Weir Electronics Co., Ltd. of China makes), model: CT-3008W-5V10mA-S1) again.Stop charging then, in water, the glove box of oxygen level, disassemble battery, take out the single order lithium-compound between graphite layers of negative pole less than 1ppm.After treating the electrolytic solution volatilization; Lithium-compound between graphite layers scraped from the copper sheet gently leave; Place in the agate mortar and grind to form uniform powder; Pour into rapidly the deionized water after in glove box, taking out powdered lithium-compound between graphite layers, deionized water described herein is as stripper, and the metallic lithium in lithium-compound between graphite layers is peeled off and made Graphene.Final gained Graphene productive rate is 0.61%, gained Graphene thickness between 0.8～12nm, promptly the number of plies between about 1～35 layer, length and width all between 100～15000nm, the strength ratio I at D peak and G peak in the Raman spectrum
D/ I
GValue is 0.74.
The SEM figure of the wherein a slice Graphene that makes for embodiment 6 shown in Figure 5.Can find out that by this SEM figure this Graphene has taken place by folding curling to a certain degree.This Graphene is studied carefully being about behind the full expand and is 10600nm, the wide 10000nm that is about.
Embodiment 7
A, solid phase pressurization prepare compound between graphite layers.
In water, the glove box of oxygen level less than 1ppm, graphite (particle diameter 40～50 μ m) 1.44g and lithium (particle diameter 200～400 μ m) 2g are mixed, place tightness system to be forced into 15kbar.Be heated to 200 ℃ afterwards, kept this pressure and temperature 24 hours, can make lithium-compound between graphite layers.
B, prepare Graphene by the compound between graphite layers that makes.
Remove the residual raw material of lithium-compound between graphite layers surface attachment, place in the agate mortar and grind to form uniform powder, in glove box, pour into rapidly the deionized water behind taking-up powdered lithium-compound between graphite layers, react immediately, thereby obtain Graphene.Final gained Graphene productive rate is 0.61%, gained Graphene thickness between 1.8～9.0nm, promptly the number of plies between about 4～26 layers, length and width all between 90～8000nm, the strength ratio I at D peak and G peak in the Raman spectrum
D/ I
GValue is 0.75.
Embodiment 8
A, solid phase pressurization prepare compound between graphite layers.
In water, the glove box of oxygen level less than 1ppm, graphite (particle diameter 40～50 μ m) 1.44g and ytterbium (particle diameter 300～500 μ m) 4g are mixed, place tightness system to be forced into 20kbar.Be heated to 390 ℃ afterwards, keep two weeks of this pressure and temperature, can get ytterbium-compound between graphite layers.
B, prepare Graphene by the compound between graphite layers that makes.
Remove the residual raw material of ytterbium-compound between graphite layers surface attachment; Place in the agate mortar and grind to form uniform powder; Pour into rapidly the deionized water after in glove box, taking out powdered ytterbium-compound between graphite layers, ytterbium-compound between graphite layers and deionized water react, and deionized water is as stripper here; Metallic lithium in ytterbium-compound between graphite layers is peeled off, thereby obtains Graphene.Final gained Graphene productive rate is 0.42%, gained Graphene thickness between 5.6～14nm, promptly the number of plies between about 15～40 layers, length and width all between 200～7600nm, the strength ratio I at D peak and G peak in the Raman spectrum
D/ I
GValue is 0.79.
Embodiment 9
A, solid phase pressurization prepare compound between graphite layers.
In water, the glove box of oxygen level less than 1ppm, graphite (diameter 40～50 μ m) 1.44g and thulium (particle diameter 300～500 μ m) 4g are mixed, place tightness system to be forced into 20kbar.Be heated to 500 ℃ afterwards, keep two weeks of this pressure and temperature, can get thulium-compound between graphite layers.
B, prepare Graphene by the compound between graphite layers that makes.
Remove the residual raw material of thulium-compound between graphite layers surface attachment, place the powder that grinds to form homogeneous in the agate mortar, in glove box, pour into rapidly the deionized water behind taking-up powdered thulium-compound between graphite layers, react immediately, thereby obtain Graphene.Final gained Graphene productive rate is 0.40%, gained Graphene thickness between 4.7～14.8nm, promptly the number of plies between about 13～43 layers, length and width all between 340～7000nm, the strength ratio I at D peak and G peak in the Raman spectrum
D/ I
GValue is 0.78.
Embodiment 10
A, scorification prepare compound between graphite layers.
In water, the glove box of oxygen level less than 1ppm; To place flat 100ml there-necked flask with the potassium 3.9g that is cut into irregular bulk and a stirrer at 400 ℃ of degassing natural graphite (graphitiferous carbon 97～98%, particle diameter 90～145 μ m) 9.6g after 12 hours of constant temperature under the vacuum.With the there-necked flask sealing, take out glove box, connect vacuum line, vacuumize, and feed helium, make bottle internal gas pressure a little more than normal atmosphere.Begin heating afterwards, temperature potassium to about 100 ℃ the time melts fully, begins to carry out fierce stirring this moment.Insulation is 45 minutes after temperature rises to 170 ℃, and cooling afterwards obtains the potassium-compound between graphite layers of single order.
B, prepare Graphene by the compound between graphite layers that makes.
Remove the residual raw material of potassium-compound between graphite layers surface attachment, place in the agate mortar and grind to form uniform powder, in glove box, pour into rapidly the deionized water behind taking-up powdered potassium-compound between graphite layers, react immediately, thereby obtain Graphene.Final gained Graphene productive rate is 0.45%, gained Graphene thickness between 0.9～6.0nm, promptly the number of plies between about 1～17 layer, length and width all between 95～9500nm, the strength ratio I at D peak and G peak in the Raman spectrum
D/ I
GValue is 0.77.
Embodiment 11
A, liquid phase interpolation prepare compound between graphite layers.
In water, the glove box of oxygen level, highly oriented pyrolytic graphite is cut into the parallelpiped of 1 * 2 * 0.3cm, at 400 ℃ of temperature, air pressure 10 less than 1ppm
-3Outgas under the torr.In 304 Stainless Steel Crucibles (internal diameter 25mm, height 17mm), hold molten lithium, the height of molten lithium is about 15mm, and the temperature of crucible is remained on 350 ± 5 ℃.Highly oriented pyrolytic graphite bar after the degassing finished is submerged in the molten lithium 6-8 hour, can obtain single order lithium-compound between graphite layers.Single order lithium-compound between graphite layers is taken out, with the stainless steel substrates residual lithium of its coated outside of pruning while hot.
B, prepare Graphene by the compound between graphite layers that makes.
Lithium-compound between graphite layers is placed the powder that grinds to form homogeneous in the agate mortar, in glove box, pour into rapidly the deionized water behind taking-up powdered lithium-compound between graphite layers, react immediately, thereby obtain Graphene.Final gained Graphene productive rate is 0.42%, gained Graphene thickness between 0.8～8.3nm, promptly the number of plies between about 1～25 layer, length and width all between 140～12000nm, the strength ratio I at D peak and G peak in the Raman spectrum
D/ I
GValue is 0.75.
Embodiment 12
A, liquid phase interpolation prepare compound between graphite layers.
In the glove box of water, oxygen fowl amount, highly oriented pyrolytic graphite is cut into the parallelpiped of 1 * 2 * 0.3cm, at 400 ℃ of temperature, pressure 10 less than 1ppm
-3Outgas under the torr.Calcium (purity >=99.99%) and lithium (purity >=99.99%) are added in 304 Stainless Steel Crucibles (internal diameter 25mm, height 17mm) according to 1: 2 mol ratio, and fusion also stirs, and add-on guarantees that the height of molten metal is about 15mm.Graphite bar after will outgasing afterwards is immersed in the liquid metal, and tightly covers crucible cover.Be incubated 10 days down at 350 ℃, take out the graphite bar afterwards while hot, scrape off top kish, can obtain triple lithium-calcium-compound between graphite layers.
B, prepare Graphene by the compound between graphite layers that makes.
Lithium-calcium-compound between graphite layers placed grind to form uniform powder in the agate mortar, pour into rapidly the deionized water after in glove box, taking out powdered lithium-calcium-compound between graphite layers, react immediately, thereby obtain Graphene.Final gained Graphene productive rate is 0.39%, gained Graphene thickness between 5.8～13.6nm, promptly the number of plies between about 15～40 layers, length and width all between 130～6700nm, the strength ratio I at D peak and G peak in the Raman spectrum
D/ I
GValue is 0.78.
Embodiment 13
A, molten salt electrolysis of metals legal system are equipped with compound between graphite layers.
As negative electrode (diameter 6mm), high purity graphite (impurity is less than 35ppm) crucible (high 140mm, internal diameter 20mm, external diameter 30mm) is as anode with high purity graphite (impurity is less than 35ppm) rod for electrolyzer, and fusion sodium-chlor is as ionogen.Use one can temperature control vertical heater and the sealing corundum tubular reactor that is connected with water cooling plant.99% pure sodium-chlor is adding in the reactor drum after super-dry, and the speed with 150ml/min pours into high-purity argon in reactor drum then, is used for the gas of purge reactor, and the inert atmosphere that keeps reactor drum is in case the generation of oxidation reaction.After continue feeding high-purity argon, begin to heat up, reach 850 ℃ after about 3 hours, treat the sodium-chlor fusing after, negative electrode is slowly inserted in the melting salt.The length of inserting in the fused salt is remained a constant.Continuous current with 5A carried out electrolysis 3 hours afterwards.After electrolysis finishes, treat the device cooling after, take out sealed reactor and transfer in water, the glove box of oxygen level less than 1ppm, scrape off sodium-chlor residual on the negative electrode, can obtain sodium-compound between graphite layers.
B, prepare Graphene by the compound between graphite layers that makes.
Sodium-compound between graphite layers placed grind to form uniform powder in the agate mortar, pour into rapidly the deionized water after in glove box, taking out powdered sodium-compound between graphite layers, react immediately, thereby obtain Graphene.Final gained Graphene productive rate is 0.39%, and gained Graphene thickness is between 3.8～9.2nm, and promptly the number of plies is between about 10～27 layers.Length and width all between 150～6700nm, the strength ratio I at D peak and G peak in the Raman spectrum
D/ I
GValue is 0.76.
Embodiment 14
A, two warm area vapor transportation legal systems are equipped with compound between graphite layers.
Natural graphite (diameter＜30 μ m) 1.92g and potassium 0.78g are respectively charged into the heat-resistant glass tube both sides, vacuumize, reach about 1.33Pa to vacuum tightness.Heat with two groups of electrothermal ovens, first heating graphite end, treat graphite end temperature rise to 450 ℃ after reheat potassium end, and make potassium end temperature maintenance at 250 ℃.Begin slowly to reduce graphite end temperature this moment, makes it remain on 280～300 ℃, heated 3 days, finally obtains bronze spherical product at the graphite end, is the potassium-compound between graphite layers that makes.Heat-resistant glass tube is transferred in water, the glove box of oxygen level less than 1ppm, taken out potassium-compound between graphite layers wherein.
B, prepare Graphene by the compound between graphite layers that makes.
Heat-resistant glass tube is transferred in water, the glove box of oxygen level less than 1ppm; Take out potassium-compound between graphite layers; Remove the residual raw material of potassium-compound between graphite layers surface attachment, place the powder that grinds to form homogeneous in the agate mortar, in glove box, pour into the deionized water rapidly behind taking-up powdered potassium-compound between graphite layers; React immediately, thereby obtain Graphene.Final gained Graphene productive rate is 0.45%, and gained Graphene thickness is between 0.8～6.7nm, and promptly the number of plies is between about 1～20 layer.Length and width all between 110～6700nm, the ratio I at D peak and G peak in the Raman spectrum
D/ I
GValue is 0.79.
Embodiment 15
A, two warm area vapor transportation legal systems are equipped with compound between graphite layers.
(median size: 220 μ m) 1.92g and strontium 1.94g are respectively charged into the heat-resistant glass tube both sides, vacuumize, and reach about 0.1MPa to vacuum tightness with natural graphite.Heat with two groups of electrothermal ovens, first heating graphite end, treat graphite end temperature rise to 600 ℃ after reheat strontium end, and make strontium end temperature maintenance at 450 ℃.Begin slowly to reduce graphite end temperature this moment, makes it remain on 480～500 ℃, heated for two weeks, finally obtains the spherical product of reddish-brown at the graphite end, is the strontium-compound between graphite layers that makes.
B, prepare Graphene by the compound between graphite layers that makes.
Heat-resistant glass tube is transferred in water, the glove box of oxygen fowl amount less than 1ppm; Take out strontium-compound between graphite layers; Remove the residual raw material of strontium-compound between graphite layers surface attachment, place the powder that grinds to form homogeneous in the agate mortar, in glove box, pour into the deionized water rapidly behind taking-up powdered strontium-compound between graphite layers; React immediately, thereby obtain Graphene.Final gained Graphene productive rate is 0.44%, gained Graphene thickness between 4.2～13.8nm, promptly the number of plies between about 11～40 layers, length and width all between 80～7800nm, the strength ratio I at D peak and G peak in the Raman spectrum
D/ I
GValue is 0.77.
Embodiment 16
The mechanically peel method is peeled off compound between graphite layers and is prepared Graphene
With the prepared lithium-compound between graphite layers of embodiment 5 said battery discharge methods is raw material, in water, the glove box of oxygen level less than 1ppm, gets 0.02g lithium-compound between graphite layers powder and is scattered in the dimethyl benzene acid amides (DMF), stirs.Then and zirconia ball (diameter 2.0-2.5mm, heavy 200g) put into a tetrafluoroethylene bottle together, the tetrafluoroethylene bottle is sealed.Utilize ball mill (use instrument as: QM-3SP2 planetary ball mill (Nanjing Univ. Instrument Factory)) with the rotating speed ball milling 30h of 300rpm.Take out the gained dispersion liquid afterwards with 4000rpm, carried out centrifugal 30 minutes, finally obtain containing the upper strata dispersion liquid of Graphene.Final gained Graphene productive rate is 0.61%, gained Graphene thickness between 0.9～4.6nm, promptly the number of plies between about 1～13 layer, length and width all between 70～8600nm, the strength ratio I at D peak and G peak in the Raman spectrum
D/ I
GValue is 0.75.
Embodiment 17
The electrolytic stripping method is peeled off compound between graphite layers and is prepared Graphene
Electrolyzer is used as negative electrode with the compound between graphite layers electrode that embodiment 5 said battery discharge methods make, and high purity graphite (impurity is less than 35ppm) crucible (high 140mm, internal diameter 20mm, external diameter 30mm) is as anode, and the fusion lithium chloride is as ionogen.Use one can temperature control vertical heater and the sealing corundum tubular reactor that is connected with water cooling plant.99% pure lithium chloride is adding in the reactor drum after super-dry, and the speed with 150ml/min pours into high-purity argon in reactor drum then, is used for the gas of purge reactor, and the inert atmosphere that keeps reactor drum is in case the generation of oxidation reaction.After continue feeding high-purity argon, begin to heat up, reach 850 ℃ after about 3 hours, treat the sodium-chlor fusing after, negative electrode is slowly inserted in the melting salt.Continuous current with 10A carried out electrolysis 3 hours afterwards.After electrolysis finishes, treat the device cooling after, take out sealed reactor and transfer in water, the glove box of oxygen level less than 1ppm, scrape off sodium-chlor residual on the negative electrode, negative electrode is cleaned with deionized water repeatedly obtains Graphene after removing impurity.Final gained Graphene productive rate is 0.61%, gained Graphene thickness between 4.5～13nm, promptly the number of plies between about 12～38 layers, length and width all between 69～5400nm, the strength ratio I at D peak and G peak in the Raman spectrum
D/ I
GValue is 0.75.
Embodiment 18～38
Stripper is peeled off method and is peeled off compound between graphite layers and prepare Graphene
With the prepared lithium-compound between graphite layers of embodiment 5 said battery discharge methods is raw material; Lithium-compound between graphite layers powder is dropped in the stripper; (use instrument at UW like ultrasonic cleaner (Chinese Shanghai section leads ultrasonic instrument ltd and makes); Model: SK2510LHC) under the 53Hz environment ultrasonic 30 minutes; Under the 500rpm rotating speed, (use instrument afterwards like flying pigeon board whizzer (Chinese Shanghai peace booth scientific instrument factory makes), model: TDL80-2B) centrifugal 90 minutes, obtain Graphene.The used stripper of present embodiment is selected from alcohol, ketone, ester, amine, sulfone, chlorobenzene, organic acid, the ionic liquid in inorganic acid aqueous solution, water phase surfactant mixture and the organic liquid in the aforementioned inorganic liquid.NMP:1-N-methyl-2-2-pyrrolidone N-wherein, DMF: dimethyl benzene acid amides.
Embodiment 39～47
Stripper is peeled off method and is peeled off compound between graphite layers and prepare Graphene.
With the prepared lithium-compound between graphite layers of embodiment 5 said battery discharge methods is raw material; Lithium-compound between graphite layers powder is dropped in the stripper; (use instrument at the 53Hz UW like ultrasonic cleaner (Chinese Shanghai section leads ultrasonic instrument ltd and makes); Model: SK2510LHC) under the environment ultrasonic 30 minutes; Under the 500rpm rotating speed, (use instrument afterwards like flying pigeon board whizzer (Chinese Shanghai peace booth scientific instrument factory makes), model: TDL80-2B) centrifugal 90 minutes, obtain Graphene.The used stripper of present embodiment is selected from two or more the mixture of component of aforementioned inorganic liquid and organic liquid.
Embodiment 48
A, scorification/solid phase pressurization combined preparation compound between graphite layers.
In water, the glove box of oxygen level less than 1ppm, graphite (particle diameter 40～50 μ m) 1.44g and potassium (particle diameter 200～400 μ m) 2g are mixed, place tightness system to be forced into 15kbar.Be heated to 200 ℃ afterwards, kept this pressure and temperature 10 hours, afterwards cooling.Utilize agate mortar that the gained solid is clayed into power.
In glove box, the gained pressed powder is placed flat 100ml there-necked flask with the potassium 1.9g that is cut into irregular bulk and a stirrer then.With the there-necked flask sealing, take out glove box, connect vacuum line, vacuumize, and feed helium, make bottle internal gas pressure a little more than normal atmosphere.Begin heating afterwards, temperature potassium to about 100 ℃ the time melts fully, begins to carry out fierce stirring this moment.After temperature rises to 150 ℃ the insulation 20 minutes, get final product potassium-compound between graphite layers.
B, stripper peel off/and the combination of mechanically peel method peels off compound between graphite layers and prepares Graphene
In glove box, remove the residual raw material on the potassium-compound between graphite layers surface of gained; Getting potassium-compound between graphite layers powder 0.02g drops in the dimethyl benzene acid amides (DMF); (use instrument at the 53Hz UW like ultrasonic cleaner (Chinese Shanghai section leads ultrasonic instrument ltd and makes); Model: SK2510LHC) under the environment ultrasonic 40 minutes; Afterwards this dispersion liquid and zirconia ball (diameter 2.0-2.5mm, heavy 200g) are put into a tetrafluoroethylene bottle together, the tetrafluoroethylene bottle is sealed.Utilize ball mill (use instrument as: QM-3SP2 planetary ball mill (Nanjing Univ. Instrument Factory)) with the rotating speed ball milling of 300rpm 25 hours.Take out the gained dispersion liquid afterwards with 4000rpm, carry out centrifugally (using instrument like flying pigeon board whizzer (Chinese Shanghai peace booth scientific instrument factory makes), model: TDL80-2B) 30 minutes, finally to obtain containing the upper strata dispersion liquid of Graphene.Final gained Graphene productive rate is 0.70%, gained Graphene thickness between 0.8～8.7nm, promptly the number of plies between about 1～25 layer, length and width all between 65～13000nm, the strength ratio I at D peak and G peak in the Raman spectrum
D/ I
GValue is 0.78.
The above only is a preferred implementation of the present invention; Should be pointed out that for those skilled in the art, under the prerequisite that does not break away from the present invention's design; Can also make some improvement and retouching, these improvement and retouching also should be regarded as in protection scope of the present invention.
Claims (13)
1. a preparation method of graphene is characterized in that, is raw material with graphite, makes compound between graphite layers through inserting metal in graphite layers, peels off said compound between graphite layers then and makes Graphene.
2. preparation method of graphene as claimed in claim 1 is characterized in that, described metal be in basic metal, earth alkali metal, the rare earth metal a kind of, two or more.
3. preparation method of graphene as claimed in claim 2 is characterized in that, described metal is a basic metal.
4. preparation method of graphene as claimed in claim 3 is characterized in that, described metal is a lithium.
5. preparation method of graphene as claimed in claim 1; It is characterized in that; The preparation method of described compound between graphite layers is selected from a kind of in the following method, two or more combination: solid phase pressurization, scorification, two warm area vapor transportation methods, liquid phase interpolation, molten salt electrolysis of metals method, battery charging and discharging method.
6. preparation method of graphene as claimed in claim 1 is characterized in that, the described method of peeling off compound between graphite layers is selected from a kind of in the following method, and two or more combination: mechanically peel, stripper are peeled off, electrolytic stripping.
7. preparation method of graphene as claimed in claim 6 is characterized in that, the described method of peeling off compound between graphite layers is that stripper is peeled off.
8. preparation method of graphene as claimed in claim 7 is characterized in that, described stripper be selected from inorganic liquid and the organic liquid a kind of, two or more.
9. preparation method of graphene as claimed in claim 8 is characterized in that described inorganic liquid is selected from water, inorganic acid aqueous solution, water phase surfactant mixture.
10. preparation method of graphene as claimed in claim 9 is characterized in that, described inorganic liquid is a water.
11. preparation method of graphene as claimed in claim 8 is characterized in that, described organic liquid is selected from: alcohol, ketone, ester, amine, sulfone, chlorobenzene, organic acid, ionic liquid.
12. Graphene that adopts the described method of claim 1-11 to make.
13. Graphene as claimed in claim 12 is characterized in that, the length of said Graphene and width are 5～15000nm, and thickness is 0.3～15nm.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201110120868.1A CN102701187B (en) | 2011-07-13 | 2011-07-13 | Graphene prepared by a kind of preparation method of Graphene and use the method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201110120868.1A CN102701187B (en) | 2011-07-13 | 2011-07-13 | Graphene prepared by a kind of preparation method of Graphene and use the method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102701187A true CN102701187A (en) | 2012-10-03 |
| CN102701187B CN102701187B (en) | 2016-03-09 |
Family
ID=46894327
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201110120868.1A Expired - Fee Related CN102701187B (en) | 2011-07-13 | 2011-07-13 | Graphene prepared by a kind of preparation method of Graphene and use the method |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN102701187B (en) |
Cited By (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102815694A (en) * | 2012-03-13 | 2012-12-12 | 华东理工大学 | Graphene preparation method, and graphene prepared through using method |
| CN103771395A (en) * | 2012-10-23 | 2014-05-07 | 海洋王照明科技股份有限公司 | Graphene material and preparation method thereof |
| CN104003372A (en) * | 2013-02-21 | 2014-08-27 | 海洋王照明科技股份有限公司 | Graphene material and preparation method thereof |
| CN104108709A (en) * | 2014-07-25 | 2014-10-22 | 深圳新宙邦科技股份有限公司 | Porous graphene and preparation method thereof |
| CN104157834A (en) * | 2014-08-26 | 2014-11-19 | 四川理工学院 | Application of spiral nanometer carbon fiber as lithium ion battery cathode material and preparation method of battery cathode |
| CN104176727A (en) * | 2013-05-28 | 2014-12-03 | 安炬科技股份有限公司 | Graphene suspended solution and making method thereof |
| CN104291327A (en) * | 2014-09-24 | 2015-01-21 | 北京化工大学常州先进材料研究院 | Method for preparing graphene by peeling graphite in electrochemical manner by using molten salt |
| CN104870364A (en) * | 2013-03-06 | 2015-08-26 | 积水化学工业株式会社 | Method for producing random-structure gic, method for producing flaked graphite dispersion, flaked graphite dispersion, and flaked graphite |
| CN105271205A (en) * | 2015-11-20 | 2016-01-27 | 复旦大学 | Method for preparing layer-number-controllable high-quality graphene through electrochemical process |
| CN105502357A (en) * | 2015-12-22 | 2016-04-20 | 成都新柯力化工科技有限公司 | Stripping agent special for preparing graphene through mechanical stripping and preparation method |
| CN105916807A (en) * | 2013-09-24 | 2016-08-31 | 康斯乔最高科学研究公司 | Exfoliation of graphite with deep eutectic solvents |
| CN106435632A (en) * | 2016-09-20 | 2017-02-22 | 南昌大学 | Preparation method for boron-doped graphene |
| CN106517166A (en) * | 2016-10-19 | 2017-03-22 | 成都新柯力化工科技有限公司 | Composite stripping agent used for preparing graphene in stripping manner through slurry stirring |
| CN106543471A (en) * | 2016-10-21 | 2017-03-29 | 华东理工大学 | The preparation method of graphene nanometer sheet and Chitosan Composites |
| CN106573780A (en) * | 2014-09-09 | 2017-04-19 | 东北泰克诺亚奇股份有限公司 | Method for producing porous graphite, and porous graphite |
| CN106672958A (en) * | 2017-01-18 | 2017-05-17 | 丽水市知科科技有限公司 | Preparation method of graphene oxide |
| CN106744888A (en) * | 2017-01-18 | 2017-05-31 | 丽水市知科科技有限公司 | A kind of preparation method of Graphene |
| CN106927444A (en) * | 2015-08-06 | 2017-07-07 | 成都中医药大学 | A kind of graphene oxide with ketenes structure and preparation method thereof |
| CN107416809A (en) * | 2017-06-01 | 2017-12-01 | 黄凯 | A kind of method for preparing graphene |
| EP3216757A4 (en) * | 2014-11-07 | 2018-04-04 | Sun, Xuyang | Method for preparing graphene by molten state inorganic salt reaction bed |
| CN107902647A (en) * | 2017-11-27 | 2018-04-13 | 广西师范大学 | A kind of method that graphene is prepared as electrolyte electrochemical cathodic disbonding graphite using TTAB |
| CN108190868A (en) * | 2018-03-06 | 2018-06-22 | 绍兴文理学院 | A kind of preparation method of grapheme material |
| CN108190959A (en) * | 2018-01-23 | 2018-06-22 | 福州大学 | A kind of method that individual layer molybdenum sulfide is prepared based on the insertion stripping of molten alkali metal liquid |
| CN108270008A (en) * | 2018-01-23 | 2018-07-10 | 福州大学 | A kind of method that single-layer graphene is prepared based on the insertion stripping of molten alkali metal liquid |
| CN108586737A (en) * | 2018-03-19 | 2018-09-28 | 厦门理工学院 | A kind of conducting polymer/graphene complex and preparation method thereof |
| CN109052314A (en) * | 2018-09-17 | 2018-12-21 | 柯良节 | A method of removing multilayer two-dimension material |
| CN110117807A (en) * | 2019-03-09 | 2019-08-13 | 深圳市中科墨磷科技有限公司 | A kind of two-dimensional material-transition metal hetero-junctions preparation of sections method |
| CN110364731A (en) * | 2018-04-09 | 2019-10-22 | 北京航空航天大学 | A kind of graphene conductive slurry |
| CN110482536A (en) * | 2019-09-25 | 2019-11-22 | 维沃泰克仪器(扬州)有限公司 | A method of graphene microchip is prepared using fused carbonate one-step electrolysis |
| CN111304673A (en) * | 2020-03-19 | 2020-06-19 | 德阳烯碳科技有限公司 | Graphite electrode for electrochemically preparing graphene and preparation method thereof |
| CN111377438A (en) * | 2020-02-28 | 2020-07-07 | 清华大学 | Graphene and preparation method thereof |
| CN114555520A (en) * | 2019-11-15 | 2022-05-27 | 株式会社Lg新能源 | Preparation method of graphene nanosheet |
| CN117383549A (en) * | 2023-02-19 | 2024-01-12 | 烯源科技无锡有限公司 | Method for preparing low-defect nanoscale graphene by physical method |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101460393A (en) * | 2006-06-08 | 2009-06-17 | 戴雷克塔普拉斯专利及科技有限公司 | Production of nano-structures |
-
2011
- 2011-07-13 CN CN201110120868.1A patent/CN102701187B/en not_active Expired - Fee Related
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101460393A (en) * | 2006-06-08 | 2009-06-17 | 戴雷克塔普拉斯专利及科技有限公司 | Production of nano-structures |
Non-Patent Citations (3)
| Title |
|---|
| LISA M. VICULIS ET AL.: "Intercalation and exfoliation routes to graphite nanoplatelets", 《JOURNAL OF MATERIALS CHEMISTRY》 * |
| 卢锦花等: "石墨层间化合物的制备、结构与应用", 《炭素技术》 * |
| 袁小亚: "石墨烯的制备研究进展", 《无机材料学报》 * |
Cited By (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102815694A (en) * | 2012-03-13 | 2012-12-12 | 华东理工大学 | Graphene preparation method, and graphene prepared through using method |
| CN103771395A (en) * | 2012-10-23 | 2014-05-07 | 海洋王照明科技股份有限公司 | Graphene material and preparation method thereof |
| CN104003372A (en) * | 2013-02-21 | 2014-08-27 | 海洋王照明科技股份有限公司 | Graphene material and preparation method thereof |
| US9919926B2 (en) | 2013-03-06 | 2018-03-20 | Sekisui Chemical Co., Ltd. | Method for producing random-structure GIC, method for producing exfoliated graphite dispersion liquid, exfoliated graphite dispersion liquid, and exfoliated graphite |
| CN104870364A (en) * | 2013-03-06 | 2015-08-26 | 积水化学工业株式会社 | Method for producing random-structure gic, method for producing flaked graphite dispersion, flaked graphite dispersion, and flaked graphite |
| CN104870364B (en) * | 2013-03-06 | 2017-09-01 | 积水化学工业株式会社 | Disordered structure GIC manufacture method, the manufacture method of sheet graphite dispersing solution, sheet graphite dispersing solution and thin slice graphite |
| CN104176727B (en) * | 2013-05-28 | 2016-04-06 | 安炬科技股份有限公司 | Graphene aaerosol solution and preparation method thereof |
| CN104176727A (en) * | 2013-05-28 | 2014-12-03 | 安炬科技股份有限公司 | Graphene suspended solution and making method thereof |
| CN105916807A (en) * | 2013-09-24 | 2016-08-31 | 康斯乔最高科学研究公司 | Exfoliation of graphite with deep eutectic solvents |
| CN104108709A (en) * | 2014-07-25 | 2014-10-22 | 深圳新宙邦科技股份有限公司 | Porous graphene and preparation method thereof |
| CN104157834B (en) * | 2014-08-26 | 2017-03-08 | 四川理工学院 | Spiral sodium rice carbon fiber is used as application and the GND preparation method of lithium ion battery negative material |
| CN104157834A (en) * | 2014-08-26 | 2014-11-19 | 四川理工学院 | Application of spiral nanometer carbon fiber as lithium ion battery cathode material and preparation method of battery cathode |
| CN106573780B (en) * | 2014-09-09 | 2019-08-02 | 东北泰克诺亚奇股份有限公司 | The preparation method and Porous Graphite of Porous Graphite |
| CN106573780A (en) * | 2014-09-09 | 2017-04-19 | 东北泰克诺亚奇股份有限公司 | Method for producing porous graphite, and porous graphite |
| CN104291327A (en) * | 2014-09-24 | 2015-01-21 | 北京化工大学常州先进材料研究院 | Method for preparing graphene by peeling graphite in electrochemical manner by using molten salt |
| EP3216757A4 (en) * | 2014-11-07 | 2018-04-04 | Sun, Xuyang | Method for preparing graphene by molten state inorganic salt reaction bed |
| CN106927444A (en) * | 2015-08-06 | 2017-07-07 | 成都中医药大学 | A kind of graphene oxide with ketenes structure and preparation method thereof |
| CN106927444B (en) * | 2015-08-06 | 2019-11-26 | 成都中医药大学 | A kind of graphene oxide and preparation method thereof with enone structure |
| CN105271205B (en) * | 2015-11-20 | 2017-12-29 | 复旦大学 | A kind of method that the controllable high-quality graphene of the number of plies is prepared using electrochemical process |
| CN105271205A (en) * | 2015-11-20 | 2016-01-27 | 复旦大学 | Method for preparing layer-number-controllable high-quality graphene through electrochemical process |
| CN105502357A (en) * | 2015-12-22 | 2016-04-20 | 成都新柯力化工科技有限公司 | Stripping agent special for preparing graphene through mechanical stripping and preparation method |
| CN106435632A (en) * | 2016-09-20 | 2017-02-22 | 南昌大学 | Preparation method for boron-doped graphene |
| CN106517166A (en) * | 2016-10-19 | 2017-03-22 | 成都新柯力化工科技有限公司 | Composite stripping agent used for preparing graphene in stripping manner through slurry stirring |
| CN106543471B (en) * | 2016-10-21 | 2018-08-07 | 华东理工大学 | The preparation method of graphene nanometer sheet and Chitosan Composites |
| CN106543471A (en) * | 2016-10-21 | 2017-03-29 | 华东理工大学 | The preparation method of graphene nanometer sheet and Chitosan Composites |
| CN106672958A (en) * | 2017-01-18 | 2017-05-17 | 丽水市知科科技有限公司 | Preparation method of graphene oxide |
| CN106744888A (en) * | 2017-01-18 | 2017-05-31 | 丽水市知科科技有限公司 | A kind of preparation method of Graphene |
| CN107416809A (en) * | 2017-06-01 | 2017-12-01 | 黄凯 | A kind of method for preparing graphene |
| CN107902647A (en) * | 2017-11-27 | 2018-04-13 | 广西师范大学 | A kind of method that graphene is prepared as electrolyte electrochemical cathodic disbonding graphite using TTAB |
| CN108270008A (en) * | 2018-01-23 | 2018-07-10 | 福州大学 | A kind of method that single-layer graphene is prepared based on the insertion stripping of molten alkali metal liquid |
| CN108190959A (en) * | 2018-01-23 | 2018-06-22 | 福州大学 | A kind of method that individual layer molybdenum sulfide is prepared based on the insertion stripping of molten alkali metal liquid |
| CN108190868A (en) * | 2018-03-06 | 2018-06-22 | 绍兴文理学院 | A kind of preparation method of grapheme material |
| CN108586737A (en) * | 2018-03-19 | 2018-09-28 | 厦门理工学院 | A kind of conducting polymer/graphene complex and preparation method thereof |
| CN110364731A (en) * | 2018-04-09 | 2019-10-22 | 北京航空航天大学 | A kind of graphene conductive slurry |
| CN109052314A (en) * | 2018-09-17 | 2018-12-21 | 柯良节 | A method of removing multilayer two-dimension material |
| CN110117807A (en) * | 2019-03-09 | 2019-08-13 | 深圳市中科墨磷科技有限公司 | A kind of two-dimensional material-transition metal hetero-junctions preparation of sections method |
| CN110482536A (en) * | 2019-09-25 | 2019-11-22 | 维沃泰克仪器(扬州)有限公司 | A method of graphene microchip is prepared using fused carbonate one-step electrolysis |
| CN114555520A (en) * | 2019-11-15 | 2022-05-27 | 株式会社Lg新能源 | Preparation method of graphene nanosheet |
| CN114555520B (en) * | 2019-11-15 | 2024-01-02 | 株式会社Lg新能源 | Preparation method of graphene nanosheets |
| CN111377438A (en) * | 2020-02-28 | 2020-07-07 | 清华大学 | Graphene and preparation method thereof |
| CN111377438B (en) * | 2020-02-28 | 2021-07-27 | 清华大学 | Graphene and preparation method thereof |
| CN111304673A (en) * | 2020-03-19 | 2020-06-19 | 德阳烯碳科技有限公司 | Graphite electrode for electrochemically preparing graphene and preparation method thereof |
| CN117383549A (en) * | 2023-02-19 | 2024-01-12 | 烯源科技无锡有限公司 | Method for preparing low-defect nanoscale graphene by physical method |
| CN117383549B (en) * | 2023-02-19 | 2024-04-26 | 烯源科技无锡有限公司 | Method for preparing low-defect nanoscale graphene by physical method |
Also Published As
| Publication number | Publication date |
|---|---|
| CN102701187B (en) | 2016-03-09 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN102701187B (en) | Graphene prepared by a kind of preparation method of Graphene and use the method | |
| CN102815694A (en) | Graphene preparation method, and graphene prepared through using method | |
| CN102868006A (en) | Method for preparing graphene through waste lithium batteries | |
| CN102791628B (en) | Material with carbon element and manufacture method thereof | |
| Wang et al. | Synthesis and manipulation of single-crystalline lithium nickel manganese cobalt oxide cathodes: A review of growth mechanism | |
| CN102070140B (en) | Method for preparing high-specific surface area graphene material by utilizing strong base chemical treatment | |
| WO2011162348A1 (en) | Silicic acid compound, positive electrode for secondary cell, and method for producing secondary cell | |
| Gauthier et al. | Melt casting LiFePO4: I. Synthesis and characterization | |
| CN102378738A (en) | Process for production of lithium iron phosphate particles and process for production of secondary battery | |
| JP2014056722A (en) | Phosphate compound, positive electrode material for secondary battery, and method for producing secondary battery | |
| CN105189346A (en) | Process for pure carbon production, compositions, and methods thereof | |
| Duan et al. | Novel efficient synthesis of nanosized carbon coated LiMnPO4 composite for lithium ion batteries and its electrochemical performance | |
| Jeong et al. | Characteristics of an electrochemical reduction of Ta2O5 for the preparation of metallic tantalum in a LiCl–Li2O molten salt | |
| Sha et al. | Appraisal of carbon-coated Li4Ti5O12 acanthospheres from optimized two-step hydrothermal synthesis as a superior anode for sodium-ion batteries | |
| WO2012067249A1 (en) | Silicate compound, secondary-battery positive electrode, secondary battery, and manufacturing methods therefor | |
| Gan et al. | Preparation of Si-SiOx nanoparticles from volatile residue produced by refining of silicon | |
| CN102583271A (en) | Spine-like SbSe3 semiconductor hydrogen storage material and preparation method thereof | |
| WO2012161055A1 (en) | Production method for material employed in energy device and/or electrical storage device, and material employed in energy device and/or electrical storage device | |
| JP2013067543A (en) | Silicate compound, positive electrode for secondary battery, and method for producing secondary battery | |
| Kawaura et al. | Scalable Synthesis of Porous Silicon by Acid Etching of Atomized Al–Si Alloy Powder for Lithium-Ion Batteries | |
| Guntlin et al. | Transition metal trifluoroacetates (M= Fe, Co, Mn) as precursors for uniform colloidal metal difluoride and phosphide nanoparticles | |
| Xu et al. | High efficiency Al-based multicomponent composites for low-temperature hydrogen production and its hydrolysis mechanism | |
| Zhang et al. | Research Development on Spinel Lithium Manganese Oxides Cathode Materials for Lithium-Ion Batteries | |
| JPWO2012057341A1 (en) | Silicic acid compound, positive electrode for secondary battery, secondary battery, and production method thereof | |
| Martins et al. | Mild hydrothermal synthesis and crystal morphology control of LiFePO4 by lithium nitrate |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20160309 Termination date: 20170713 |
|
| CF01 | Termination of patent right due to non-payment of annual fee |