CN101997120A - Lithium ion battery conductive additive and preparation method thereof - Google Patents
Lithium ion battery conductive additive and preparation method thereof Download PDFInfo
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Abstract
The invention discloses a lithium ion battery conductive additive and a preparation method thereof, and solves the technical problems of improving the conductive performance and cycle life of anode and cathode materials of a lithium ion battery. The lithium ion battery conductive additive is graphene, is black powder with grain size distribution of between 10 nanometers and 100 microns, and is a carbonaceous material consisting of single or 1,000 parallel or approximately parallel graphene lamellae. The preparation method comprises oxidization and stripping reduction. Compared with the prior art, the additive has higher electric conductivity; when the additive is applied to the electrode material, the performance of the conventional battery can be greatly improved only by a little amount; the material serving as the conductive additive has good conductive performance, is easy for dispersion, and can effectively enhance the conductive performance and the magnification charging and discharging performance of the electrode material of the lithium ion battery and prolong the cycle life; and the preparation method has low requirements for raw materials and equipment, is easy to control the process, and is suitable for industrialized production.
Description
Technical field
The present invention relates to a kind of lithium ion battery material and preparation method thereof, particularly conductive additive of a kind of lithium ion battery material and preparation method thereof.
Technical background
The Graphene of two-dimensional structure is the elementary cell that forms various sp2 hydridization material with carbon elements, and graphite is typical case's representative of being piled up the sp2 hydridization material with carbon element with layer structure that forms by the Graphene lamella, and carbon nano-tube also can be regarded as and is curled into Graphene cylindraceous.After the layer structure of graphite is determined, along with the fullerene-based material of zero dimension, the carbon nano-tube material of one dimension, especially the discovery in succession of Single Walled Carbon Nanotube has caused that can people produce great interest by stable existence for the ideal graphite alkene sheet layer material of two dimension.Past, people thought always, and strict two dimensional crystal has unsteadiness on thermodynamics, were impossible exist.2004, people such as the Novoselov of Univ Manchester UK utilized the mechanical stripping method to obtain the Graphene lamella of individual layer, bilayer and three layers first, and this Graphene lamella can be in external environment stable existence.2007, people such as Meyer reported the single-layer graphene lamella that can freely be attached on the micro metal support in vacuum or air, and these lamellas have only a carbon atom thickness 0.35nm, but showed the crystallographic order of long-range.The Graphene lamella of free state can this discovery of stable existence have been overthrown the argumentation of always putative " perfectly two dimensional crystal structure can't under non-absolute zero stable existence ".The Graphene individual layer of free state is the thinnest material that manually makes in the world at present, also is first two-dimensional material truly.It shows many peculiar electrical properties, becomes the focus of present condensed state physics research.In single-layer graphene, each carbon atom is all contributed the not electronics of Cheng Jian, and these electronics can move freely in crystal, give Graphene very good conductivity, and the typical conduction velocity of electronics is 8 * 10 in the Graphene
5M/s, more faster than the electrical conductivity speed in the general semiconductor.The band structure of the uniqueness that it has is separated from each other hole and electronics, has caused the generation of new electrical conductivity phenomenon, for example irregular quantum hall effect.
Known graphene preparation method comprises mechanical stripping method, SiC pyrolysismethod, chemical vapour deposition technique, carbon nano-tube patterning method at present.The mechanical stripping method is to go out the Graphene lamella by mechanical force from fresh graphite crystal sur-face peeling, and the Graphene lamella yardstick that uses this method to obtain can reach about 100 μ m; The SiC pyrolysismethod is to remove Si by heating 6H-SiC monocrystalline, decomposites the Graphene lamella on specific single facet; Chemical vapour deposition (CVD) is to be matrix with transition metal such as Ni, Ru, utilizes the carbon atom of carbon source cracking to separate out at matrix surface, obtains the Graphene of single or multiple lift; Carbon nano-tube cutting rule is to utilize laser that thereby the curling lamella of carbon nano-tube is axially cut acquisition individual layer and multi-layer graphene.
In said method, for the mechanical stripping method, the Graphene and the very difficult sub-argument that only can access minute quantity go out pure individual layer or which floor Graphene; For heating SiC method, though can control the number of plies of Graphene by the control heating-up temperature, severe reaction conditions and can't carry out large-scale production; Also there is same problem in chemical vapour deposition (CVD), and the regular deposition of carbon atom bunch can only occur on some specific matrix and the number of plies is difficult to accurate control; Operating on the Nano grade of carbon nano-tube patterning method, high to equipment precision requirement, only can study at present at laboratory level.
In lithium ion battery negative material and Research on conductive material, be still everybody and pay close attention to and one of the emphasis of research as studying for people the earliest and being applied to the business-like carbonaceous material of lithium ion battery, research emphasis from now on is still how better utilizes cheap native graphite and develops valuable amorphous carbon material.The lithium rechargeable battery of prior art mainly uses electrically conductive graphite, acetylene black and carbon nano-tube as conductive additive, the chain thing that acetylene black is made up of amorphous carbon particle spherical in shape, it is present the most widely used conductive additive, cheap, but in order to reach the purpose that contacts with each other between the intensifier electrode active material, needed addition is bigger, thereby causes the decline of electrode capacity; Carbon nano-tube is the one dimension carbonaceous material that is line style, compare with acetylene black, carbon nano-tube has better electric conductivity and addition still less, but costing an arm and a leg of carbon current nanotube, and the shortcoming that has difficulties in dispersion when using as conductive additive becomes and hinders the principal element that it is further used.
Summary of the invention
The purpose of this invention is to provide a kind of lithium ion battery conductive additive and preparation method thereof, the technical problem of solution is to improve the electric conductivity and the cycle life of lithium ion battery positive and negative electrode material, the professional etiquette of going forward side by side modelling industrial production.
The present invention is by the following technical solutions: a kind of lithium ion battery conductive additive, described lithium ion battery conductive additive is a Graphene, be the black powder of particle size distribution between 10nm-100 μ m, be layer to parallel or approach the carbonaceous material that parallel Graphene lamella constitutes by individual layer-1000, specific area is 50-1500m
2/ g, conductivity is 1 * 10
4-9 * 10
4S/m.
A kind of preparation method of lithium ion battery conductive additive, may further comprise the steps: one, strongly acidic solution is cooled to 0-4 ℃, with carbon content at the natural flake graphite powder more than 94%, the mixture of potassium nitrate and/or sodium nitrate adds in the strongly acidic solution, under the mixing speed of 60-3000rpm, after adding strong oxidizer potassium permanganate, continue to stir 0.5-12h, this mixture temperature is controlled in the 32-38 ℃ of scope, continue to stir 0.5-12h again, add volume 0.5-4 doubly to the deionized water of employed strongly acidic solution, make this mixture system temperature be controlled at 85-100 ℃, after continuing to stir 15min-2h, add deionized water and make the volume of mixture system increase 1-2 doubly, add hydrogenperoxide steam generator again, filter after mixing, washing does not have SO to filtrate
4 2-Ion keeps 2-96h under 50-120 ℃, atmosphere or vacuum condition, obtain the graphite oxide powder; Described graphite powder: strongly acidic solution: nitrate: strong oxidizer: the hydrogen peroxide mass ratio is: 1: 10-50: 0.5-2: 30-60: 1-5; Two, with graphite oxide powder nitrogen, helium or argon gas deaeration, subsequently under vacuum degree is lower than atmospheric pressure, to 200-1000 ℃, keep 5min-24h with the programming rate of 5-100 ℃/min, naturally cool to room temperature then, the graphene oxide powder that obtains peeling off; Or press mass ratio 1: 2-20, the graphite oxide powder is scattered in deionized water or the ethanol, at ultrasonic frequency 20-25kHz, power density 30-650W/cm
2, sonic oscillation is handled 5min-5h, the graphene oxide solution that obtains peeling off under the temperature 4-50 ℃ condition; Or press mass ratio 1: 2-20, and the graphite oxide powder is scattered in deionized water or the ethanol, under the rotating speed of 1000-8000rpm, stir 10min-5h, the graphene oxide solution that obtains peeling off; Three, with the graphene oxide powder of peeling off, or the graphene oxide solution of peeling off joins in the liquid reducer solution, the graphene oxide powder of peeling off and the mass ratio of liquid reducer are 1: 0.5-10, under 0-70 ℃ bath temperature, kept 0.5-24 hour, filter then, washing keeps 2-96h under 50-120 ℃, atmosphere or vacuum condition, obtain the lithium ion battery conductive additive; Maybe with graphite oxide powder nitrogen, helium or the argon gas deaeration peeled off, subsequently with the programming rate of 5-100 ℃/min to 200-1000 ℃, nitrogen, helium or argon gas are switched to reducibility gas, flow is 10ml/min-10L/min, under this temperature, keep 5min-24h, naturally cool to room temperature then, obtain the lithium ion battery conductive additive.
Method strongly acidic solution of the present invention is the concentrated sulfuric acid, red fuming nitric acid (RFNA) or perchloric acid, and concentrated sulfuric acid concentration is not less than 70%, and red fuming nitric acid (RFNA) is not less than 65%, and perchloric acid concentration is not less than 60%.
Method of the present invention is cooled to 0 ℃ with strongly acidic solution.
Method graphite powder granularity of the present invention is less than 30 orders.
Method of the present invention adds 2 times of deionized water volumes to employed strongly acidic solution.
Method of the present invention adds 2 times of deionized water volumes to employed strongly acidic solution, makes this mixture system temperature be controlled at 95-98 ℃.
The HCl solution that method of the present invention is cleaned with 5% washs filter cake, uses the deionized water wash filter cake then.
Method liquid reducer of the present invention is sodium borohydride or solution of potassium borohydride, or the solution of amine and soluble derivative thereof: hydrazine hydrate, to diphenylamines, adjacent diphenylamines or a diphenylamines, its chemical general formula is: X-NH2, wherein X is NH2, R
1NH2, NHOH, NHR
1OH or NHR
1OHR
2OH, R
1, R
2For phenyl ring or-(CH2)
n-, n=1,2,3 ... 10.
Method reducibility gas of the present invention is hydrogen or carbon monoxide.
The present invention compared with prior art, set out by graphite type material, through peroxidating, peel off and reduce processing, obtain thin layer nano-graphene material, has higher conductivity, be applied in the electrode material, only use addition seldom just can significantly improve the performance that has battery now, this material is as conductive additive, and electric conductivity is good, be easy to disperse, can effectively strengthen the electric conductivity and the rate charge-discharge performance of lithium ion battery electrode material, improve cycle life, its preparation method is lower to the requirement of raw material and equipment, technical process is controlled easily, is fit to suitability for industrialized production.
Description of drawings
Fig. 1 is the low power SEM figure of the embodiment of the invention 1 prepared grapheme material.
Fig. 2 is the high power SEM figure of the embodiment of the invention 1 prepared grapheme material.
Fig. 3 is the low power TEM figure of the embodiment of the invention 1 prepared grapheme material.
Fig. 4 is the high power TEM figure of the embodiment of the invention 1 prepared grapheme material.
Embodiment
Below in conjunction with drawings and Examples the present invention is described in further detail.
Lithium ion battery conductive additive of the present invention is Graphene, is the black powder of particle size distribution between 10nm-100 μ m, is layer to parallel or approach the carbonaceous material that parallel Graphene lamella constitutes by individual layer-1000, and specific area is 50-1500m
2/ g, conductivity is 1 * 10
4-9 * 10
4S/m.
The preparation method of lithium ion battery conductive additive of the present invention adopts oxidation, the preparation technology that peels off, reduces, and may further comprise the steps:
One, the oxidation of graphite: under the room temperature, strongly acidic solution is placed container, adopt the DC-2006 type low temperature thermostat bath of the new sesame bio tech ltd in Ningbo, water-bath is cooled to 0-4 ℃, be preferably 0 ℃, the mixture of graphite powder and nitrate is added in the above-mentioned strongly acidic solution, adopt Jintan City, Jiangsu Province Jin Cheng state to win the JJ-1 type timing electric mixer of laboratory apparatus factory, under the mixing speed of 60-3000rpm, slowly add strong oxidizer, after treating that strong oxidizer is reinforced and finishing, continue to stir 0.5-12h, this mixture temperature is controlled in the 32-38 ℃ of scope then, continue to stir 0.5-12h again, slowly add volume 0.5-4 subsequently doubly, be preferably 2 times of deionized waters to employed strongly acidic solution, make this mixture system temperature be controlled at 85-100 ℃, be preferably 95-98 ℃, after continuing to stir 15min-2h, make the volume of mixture system increase 1-2 doubly, add hydrogenperoxide steam generator again to wherein adding deionized water, filter after mixing, and with 5% HCl solution filter cake is washed, use the deionized water wash filter cake then, in filtrate, there is not SO
4 2-Ion places filter cake in the DZF-6050 type vacuum drying chamber of the grand experimental facilities of Nereid Co., Ltd and carries out dried, keeps 2-96h under 50-120 ℃, atmosphere or vacuum condition, obtains the graphite oxide powder.The mass ratio of above-mentioned each reactant is: graphite powder: strongly acidic solution: nitrate: strong oxidizer: hydrogen peroxide=1: 10-50: 0.5-2: 30-60: 1-5.
Described graphite powder be granularity less than 30 orders, carbon content at the natural flake graphite more than 94%.
Described strongly acidic solution is the concentrated sulfuric acid, red fuming nitric acid (RFNA) or perchloric acid, and wherein concentrated sulfuric acid concentration is not less than 70%, and red fuming nitric acid (RFNA) is not less than 65%, and perchloric acid concentration is not less than 60%.
Described nitrate is potassium nitrate and/or sodium nitrate.
Described strong oxidizer is a potassium permanganate.
Two, peeling off of graphite oxide:
First method; heat treatment is peeled off; the graphite oxide powder is placed unlimited quartz boat; put into CVD-(D) the type low temperature tube furnace of Hefei Risine Heatek Co., Ltd.; with protective gas furnace chamber is carried out exhaust to remove the air in the furnace chamber; vacuumize subsequently; make the interior vacuum degree of stove be lower than atmospheric pressure; with the programming rate of 5-100 ℃/min to 200-1000 ℃; keep 5min-24h, in stove, naturally cool to room temperature then, between temperature raising period with stove; tangible volumetric expansion takes place in the graphite oxide powder, the graphene oxide powder that obtains peeling off.
Nitrogen, helium or the argon gas of described protective gas for not reacting with graphite.
Second method, ultrasonic wave is peeled off, press mass ratio 1: 2-20, the graphite oxide powder is scattered in deionized water or the ethanol, this mixture solution is placed the JY92-IIN type cell Ultrasonic Cell Disruptor of Ningbo Xin Zhi Bioisystech Co., Ltd, at ultrasonic frequency 20-25kHz, power density 30-650W/cm
2, sonic oscillation is handled 5min-5h under the temperature 4-50 ℃ condition, that realizes graphite oxide peels off the graphene oxide solution that obtains peeling off.
The third method, stirring is peeled off, press mass ratio 1: 2-20, the graphite oxide powder is scattered in deionized water or the ethanol, this mixture solution is put into the Changzhou Wujin F-0.4 type high speed dispersor of machinery plant from all directions, under the rotating speed of 1000-8000rpm, stir 10min-5h, peel off the graphene oxide solution that obtains peeling off with what realize graphite oxide.
Three, the reduction of graphene oxide:
First method, liquid-phase reduction, with the graphene oxide powder of peeling off, or the graphene oxide solution of peeling off joins in the liquid reducer solution, the graphene oxide powder of peeling off (if the graphene oxide solution of peeling off, then be meant solids content wherein) with the mass ratio of liquid reducer be 1: 0.5-10, the container that fills this mixture solution is placed water-bath, under 0-70 ℃ bath temperature, kept 0.5-24 hour, filter then, and filter cake is washed with deionized water, filter cake is placed in the DZF-6050 type vacuum drying chamber of the grand experimental facilities of Nereid Co., Ltd, at 50-120 ℃, atmosphere or vacuum condition keep 2-96h down, carry out drying, obtain the nano-graphene powder, i.e. the lithium ion battery conductive additive.
Described liquid reducer is sodium borohydride or solution of potassium borohydride, or the solution of amine and soluble derivative thereof: hydrazine hydrate, to diphenylamines, adjacent diphenylamines or a diphenylamines, its chemical general formula is: X-NH2, wherein X is NH2, R
1NH2, NHOH, NHR
1OH or NHR
1OHR
2OH, R
1, R
2For phenyl ring or-(CH2)
n-, n=1,2,3 ... 10.
Second method; vapour phase reduction; the graphite oxide powder of peeling off is placed unlimited quartz boat; put into CVD-(D) the type low temperature tube furnace of Hefei Risine Heatek Co., Ltd.; with protective gas furnace chamber is carried out exhaust to remove the air in the furnace chamber; subsequently with the programming rate of 5-100 ℃/min to 200-1000 ℃; protective gas is switched to reducibility gas; gas flow is 10ml/min-10L/min; and under this temperature, keep 5min-24h; in stove, naturally cool to room temperature then, obtain the Graphene powder body material, be i.e. the lithium ion battery conductive additive with stove.
Nitrogen, helium or the argon gas of described protective gas for not reacting with graphite.
Described reducibility gas is hydrogen or carbon monoxide.
The lithium ion battery conductive additive of method preparation of the present invention, adopt Hitachi S-4800 type scanning electron microscopy SEM that pattern is observed, adopt the JEM-1230 type transmission electron microscope TEM of Jeol Ltd. that microstructure is observed, with Quantachrome NOVA 1000e type ratio table ﹠amp; Aperture tester contrast table area is tested, and uses the marine rainbow fortune FZ-9601 of instrument plant type powder resistivity tester this additive agent powder conductivity of electrolyte materials is tested.
Lithium ion battery conductive additive with method preparation of the present invention carries out the produced with combination anode with lithium cell anode material lithium manganate or LiFePO 4.Positive electrode, conductive additive, binding agent PVDF are according to mass ratio 90-96: 2-5: 2-5, after making solvent and evenly size mixing with N-methyl pyrrolidone NMP, be applied on the aluminium foil, dry down at 120 ℃, pass through roll-in, cut-parts, coiling, fluid injection, packaging process then, make 18650 cylindrical batteries, employed negative material is carbonaceous mesophase spherules MCMB, barrier film is Celgard2400, and electrolyte is 1MLiPF
6/ EC+DMC+EMC.
Lithium ion battery conductive additive with method preparation of the present invention carries out the produced with combination battery cathode with lithium ion battery negative material carbonaceous mesophase spherules MCMB or native graphite.Negative material, conductive additive, binding agent SBR, thickener CMC are according to mass ratio 90-95: 1-5: 2-3: 1-2, after evenly sizing mixing as solvent with water, be coated on the Copper Foil, dry down at 100 ℃, pass through roll-in, cut-parts, coiling, fluid injection, packaging process then, make 18650 cylindrical batteries, employed positive electrode is a LiFePO 4, barrier film is Celgard2400, and electrolyte is 1MLiPF
6/ EC+DMC+EMC.
On the BS-303Q of Qingtian Industry Co., Ltd., Guangzhou type secondary cell automatic checkout equipment, above-mentioned battery is carried out electrochemical property test, content measurement comprise the internal resistance of cell, different multiplying discharge and recharge under the condition capability retention and at separately the capability retention after 500 weeks of circulation of charging and discharging under voltage, the 1C charging and discharging currents density.
The technological parameter of embodiment 1-9 sees Table 1.
Table 1 embodiment 1-9 technological parameter
The Graphene powder that embodiment 1 prepares, after tested, specific area is 200-400m
2/ g, conductivity is 5 * 10
4-9 * 10
4S/m.As depicted in figs. 1 and 2, the black powder of particle size distribution between 5-50 μ m.As shown in Figure 3 and Figure 4, be to parallel or approach the carbonaceous material that parallel Graphene lamella constitutes by the 5-500 layer.
Graphene powder and lithium iron phosphate cathode material that embodiment 1 is prepared carry out compound, the manufacture method of anode pole piece is as follows: lithium iron phosphate cathode material, conductive additive, binding agent PVDF were according to mass ratio 94: 3: 3, make solvent with NMP, in mixer, stir 4h with the 2000rpm rotating speed, slurry after mixing is applied on the aluminium foil, dry under 120 ℃, pass through roll-in then, obtain anode pole piece; Pass through again cut-parts, with barrier film and cathode pole piece coiling, fluid injection, packaging process in order, make 18650 cylindrical batteries, carry out electrochemical property test.
Comparative Examples 1, adopt carbon black to carry out compound as conductive additive and positive electrode material LiFePO 4 of lithium, wherein lithium iron phosphate cathode material, conductive black, binding agent PVDF were according to mass ratio 91: 5: 4, make solvent with NMP, in mixer, stir 6h, the slurry after mixing is applied on the aluminium foil with the 2000rpm rotating speed, dry down at 120 ℃, pass through roll-in then, obtain anode pole piece; Pass through again cut-parts, with barrier film and cathode pole piece coiling, fluid injection, packaging process in order, make 18650 cylindrical batteries of Comparative Examples 1.
Embodiment 1 is identical with employed cathode pole piece in the Comparative Examples 1, its manufacture method is as follows: negative material carbonaceous mesophase spherules MCMB, graphene conductive additive, binding agent SBR, thickener sodium carboxymethylcellulose CMC were according to mass ratio 94: 2: 2.5: 1.5, with water as solvent, in mixer, stir 5h with the 1500rpm rotating speed, slurry after mixing is coated on the Copper Foil, dry under 120 ℃, pass through roll-in then, obtain cathode pole piece.
Stir easily in the Graphene powder of embodiment 1 and the cell positive material allotment slurry process, be difficult for taking place the reunion sedimentation phenomenon, with Comparative Examples 1 relatively when sizing mixing with identical mixing speed the slurry viscosity value reach that to stablize the needed time shorter.The electric performance test of embodiment 1 and Comparative Examples 1 sees Table 2.
Table 2 embodiment 1 and Comparative Examples 1 electric performance test result
Graphene powder and positive-material lithium manganate that embodiment 2 is prepared carry out compound, manganate cathode material for lithium, conductive additive, binding agent PVDF were according to mass ratio 95: 2: 3, make solvent with NMP, in mixer, stir 4h with the 2000rpm rotating speed, slurry after mixing is applied on the aluminium foil, dry under 120 ℃, pass through roll-in then, obtain anode pole piece; Pass through again cut-parts, with barrier film and cathode pole piece coiling, fluid injection, packaging process in order, make 18650 cylindrical batteries.
Comparative Examples 2, adopt carbon black to carry out compound as conductive additive and positive-material lithium manganate, wherein positive electrode, conductive black, binding agent PVDF were according to mass ratio 91: 5: 4, make solvent with NMP, in mixer, stir 6h, the slurry after mixing is applied on the aluminium foil with the 2000rpm rotating speed, dry down at 120 ℃, pass through roll-in then, obtain anode pole piece; Pass through again cut-parts, with barrier film and cathode pole piece coiling, fluid injection, packaging process in order, make 18650 cylindrical batteries of Comparative Examples 2.
Embodiment 2 is identical with employed cathode pole piece in the Comparative Examples 2, and its manufacture method is identical with cathode pole piece in embodiment 1 and the Comparative Examples 1.The electric performance test of embodiment 2 and Comparative Examples 2 sees Table 3.
Table 3 embodiment 2 and Comparative Examples 2 electric performance test results
Graphene powder and lithium ion battery negative material native graphite that embodiment 3 is prepared carry out the produced with combination battery cathode.The manufacture method of cathode pole piece is as follows: graphite cathode material, conductive additive Graphene powder, binding agent SBR, thickener CMC were according to mass ratio 94: 2: 2.5: 1.5, with water as solvent, in mixer, stir 3h with the 1500rpm rotating speed, slurry after mixing is coated on the Copper Foil, dry down at 100 ℃, pass through roll-in then, obtain cathode pole piece; Pass through again cut-parts, with barrier film and anode pole piece coiling, fluid injection, packaging process in order, make 18650 cylindrical batteries.
Comparative Examples 3, adopt conductive black to carry out compound as conductive additive and graphite cathode material, wherein graphite cathode material, conductive black, binding agent SBR, thickener CMC were according to mass ratio 94: 2: 2.5: 1.5, with water as solvent, in mixer, stir 5h with the 1500rpm rotating speed, slurry after mixing is coated on the Copper Foil, dry under 120 ℃, obtain cathode pole piece; Pass through again cut-parts, with barrier film and anode pole piece coiling, fluid injection, packaging process in order, make 18650 cylindrical batteries of Comparative Examples 3.
Embodiment 3 is identical with employed anode pole piece in the Comparative Examples 3, and its manufacture method is identical with ferrous lithium phosphate cathode pole piece among the embodiment 1.The electric performance test of embodiment 3 and Comparative Examples 3 sees Table 4.
Table 4 embodiment 3 and Comparative Examples 3 electric performance test results
Claims (10)
1. lithium ion battery conductive additive, it is characterized in that: described lithium ion battery conductive additive is a Graphene, be the black powder of particle size distribution between 10nm-100 μ m, be layer to parallel or approach the carbonaceous material that parallel Graphene lamella constitutes by individual layer-1000, specific area is 50-1500m
2/ g, conductivity is 1 * 10
4-9 * 10
4S/m.
2. the preparation method of a lithium ion battery conductive additive, may further comprise the steps: one, strongly acidic solution is cooled to 0-4 ℃, with carbon content at the natural flake graphite powder more than 94%, the mixture of potassium nitrate and/or sodium nitrate adds in the strongly acidic solution, under the mixing speed of 60-3000rpm, after adding strong oxidizer potassium permanganate, continue to stir 0.5-12h, this mixture temperature is controlled in the 32-38 ℃ of scope, continue to stir 0.5-12h again, add volume 0.5-4 doubly to the deionized water of employed strongly acidic solution, make this mixture system temperature be controlled at 85-100 ℃, after continuing to stir 15min-2h, add deionized water and make the volume of mixture system increase 1-2 doubly, add hydrogenperoxide steam generator again, filter after mixing, washing does not have SO to filtrate
4 2-Ion keeps 2-96h under 50-120 ℃, atmosphere or vacuum condition, obtain the graphite oxide powder; Described graphite powder: strongly acidic solution: nitrate: strong oxidizer: the hydrogen peroxide mass ratio is: 1: 10-50: 0.5-2: 30-60: 1-5; Two, with graphite oxide powder nitrogen, helium or argon gas deaeration, subsequently under vacuum degree is lower than atmospheric pressure, to 200-1000 ℃, keep 5min-24h with the programming rate of 5-100 ℃/min, naturally cool to room temperature then, the graphene oxide powder that obtains peeling off; Or press mass ratio 1: 2-20, the graphite oxide powder is scattered in deionized water or the ethanol, at ultrasonic frequency 20-25kHz, power density 30-650W/cm
2, sonic oscillation is handled 5min-5h, the graphene oxide solution that obtains peeling off under the temperature 4-50 ℃ condition; Or press mass ratio 1: 2-20, and the graphite oxide powder is scattered in deionized water or the ethanol, under the rotating speed of 1000-8000rpm, stir 10min-5h, the graphene oxide solution that obtains peeling off; Three, with the graphene oxide powder of peeling off, or the graphene oxide solution of peeling off joins in the liquid reducer solution, the graphene oxide powder of peeling off and the mass ratio of liquid reducer are 1: 0.5-10, under 0-70 ℃ bath temperature, kept 0.5-24 hour, filter then, washing keeps 2-96h under 50-120 ℃, atmosphere or vacuum condition, obtain the lithium ion battery conductive additive; Maybe with graphite oxide powder nitrogen, helium or the argon gas deaeration peeled off, subsequently with the programming rate of 5-100 ℃/min to 200-1000 ℃, nitrogen, helium or argon gas are switched to reducibility gas, flow is 10ml/min-10L/min, under this temperature, keep 5min-24h, naturally cool to room temperature then, obtain the lithium ion battery conductive additive.
3. the preparation method of lithium ion battery conductive additive according to claim 2, it is characterized in that: described strongly acidic solution is the concentrated sulfuric acid, red fuming nitric acid (RFNA) or perchloric acid, concentrated sulfuric acid concentration is not less than 70%, and red fuming nitric acid (RFNA) is not less than 65%, and perchloric acid concentration is not less than 60%.
4. the preparation method of lithium ion battery conductive additive according to claim 3 is characterized in that: described strongly acidic solution is cooled to 0 ℃.
5. the preparation method of lithium ion battery conductive additive according to claim 4 is characterized in that: described graphite powder granularity is less than 30 orders.
6. the preparation method of lithium ion battery conductive additive according to claim 5 is characterized in that: 2 times of described adding deionized water volumes are to employed strongly acidic solution.
7. the preparation method of lithium ion battery conductive additive according to claim 6 is characterized in that: 2 times of described adding deionized water volumes make this mixture system temperature be controlled at 95-98 ℃ to employed strongly acidic solution.
8. the preparation method of lithium ion battery conductive additive according to claim 7 is characterized in that: described cleaning is washed filter cake with 5% HCl solution, uses the deionized water wash filter cake then.
9. the preparation method of lithium ion battery conductive additive according to claim 8, it is characterized in that: described liquid reducer is sodium borohydride or solution of potassium borohydride, or the solution of amine and soluble derivative thereof: hydrazine hydrate, to diphenylamines, adjacent diphenylamines or a diphenylamines, its chemical general formula is: X-NH2, wherein X is NH2, R
1NH2, NHOH, NHR
1OH or NHR
1OHR
2OH, R
1, R
2For phenyl ring or-(CH2)
n-, n=1,2,3 ... 10.
10. the preparation method of lithium ion battery conductive additive according to claim 9 is characterized in that: described reducibility gas is hydrogen or carbon monoxide.
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| CN2010105033215A CN101997120A (en) | 2010-10-09 | 2010-10-09 | Lithium ion battery conductive additive and preparation method thereof |
| CN201110157325.7A CN102263265B (en) | 2010-10-09 | 2011-06-13 | Conductive additives for lithium-ion batteries and preparation method of conductive additives |
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