CN102593464A - Current collector and preparation method thereof - Google Patents
Current collector and preparation method thereof Download PDFInfo
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- CN102593464A CN102593464A CN2012100504108A CN201210050410A CN102593464A CN 102593464 A CN102593464 A CN 102593464A CN 2012100504108 A CN2012100504108 A CN 2012100504108A CN 201210050410 A CN201210050410 A CN 201210050410A CN 102593464 A CN102593464 A CN 102593464A
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- 238000002360 preparation method Methods 0.000 title claims abstract description 27
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 94
- 229910021389 graphene Inorganic materials 0.000 claims abstract description 76
- 238000000576 coating method Methods 0.000 claims abstract description 67
- 239000011248 coating agent Substances 0.000 claims abstract description 64
- 239000002002 slurry Substances 0.000 claims abstract description 53
- 239000011230 binding agent Substances 0.000 claims abstract description 30
- 239000011888 foil Substances 0.000 claims abstract description 27
- 239000002904 solvent Substances 0.000 claims abstract description 11
- 238000001035 drying Methods 0.000 claims abstract description 6
- 238000000034 method Methods 0.000 claims description 22
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 20
- 238000003756 stirring Methods 0.000 claims description 9
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 150000001336 alkenes Chemical class 0.000 claims description 6
- 229910002804 graphite Inorganic materials 0.000 claims description 6
- 239000010439 graphite Substances 0.000 claims description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 5
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 4
- 239000004917 carbon fiber Substances 0.000 claims description 4
- 239000006185 dispersion Substances 0.000 claims description 4
- 239000012046 mixed solvent Substances 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 239000006230 acetylene black Substances 0.000 claims description 3
- 238000004945 emulsification Methods 0.000 claims description 3
- 238000007581 slurry coating method Methods 0.000 claims description 3
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000011149 active material Substances 0.000 abstract description 21
- 239000011247 coating layer Substances 0.000 abstract description 11
- 239000010410 layer Substances 0.000 abstract description 9
- 238000007599 discharging Methods 0.000 abstract description 4
- 230000001070 adhesive effect Effects 0.000 abstract description 3
- 239000000853 adhesive Substances 0.000 abstract description 2
- 230000009467 reduction Effects 0.000 abstract description 2
- 238000000926 separation method Methods 0.000 abstract 1
- 238000012360 testing method Methods 0.000 description 29
- 239000005030 aluminium foil Substances 0.000 description 12
- 239000008367 deionised water Substances 0.000 description 12
- 229910021641 deionized water Inorganic materials 0.000 description 12
- 238000005303 weighing Methods 0.000 description 10
- 239000007788 liquid Substances 0.000 description 8
- 239000000523 sample Substances 0.000 description 8
- ZPOLNCDBPYJDSE-UHFFFAOYSA-N 3-[4-[bis(2-chloroethyl)amino]phenyl]-2-formamidopropanoic acid Chemical compound O=CNC(C(=O)O)CC1=CC=C(N(CCCl)CCCl)C=C1 ZPOLNCDBPYJDSE-UHFFFAOYSA-N 0.000 description 7
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 7
- 239000001768 carboxy methyl cellulose Substances 0.000 description 7
- 150000004040 pyrrolidinones Chemical class 0.000 description 7
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 7
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 7
- 238000012545 processing Methods 0.000 description 6
- 238000012546 transfer Methods 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 5
- 239000011889 copper foil Substances 0.000 description 5
- 229910052744 lithium Inorganic materials 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- -1 Kynoar Polymers 0.000 description 4
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 229910001416 lithium ion Inorganic materials 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
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- 230000008569 process Effects 0.000 description 4
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- 239000006229 carbon black Substances 0.000 description 3
- 239000004020 conductor Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000001132 ultrasonic dispersion Methods 0.000 description 3
- 241000446313 Lamella Species 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000004146 energy storage Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- 230000002411 adverse Effects 0.000 description 1
- 238000000627 alternating current impedance spectroscopy Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 238000012983 electrochemical energy storage Methods 0.000 description 1
- 238000003487 electrochemical reaction Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
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- 238000004381 surface treatment Methods 0.000 description 1
Images
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
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- Battery Electrode And Active Subsutance (AREA)
- Cell Electrode Carriers And Collectors (AREA)
Abstract
The invention provides a current collector and a preparation method thereof. The current collector comprises a current collector foil and at least one surface of the current collector foil is coated with coating layers containing graphene and a binder. The preparation method comprises the following steps of dispersing graphene and the binder in a solvent to obtain slurry, coating the slurry on at least one surface of the current collector foil and drying. Graphene of the coating layer has a two-dimensional sheet structure and thus the graphene forms a uniform and compact coating on the surface of the current collector foil so that a contact area of the graphene and the surface of the current collector is greatly improved; a conductive contact between an active material and the current collector is improved; the interface resistance of the current collector and the active material is effectively reduced; and internal resistance of a cell is reduced. Contact areas of graphene layers paved on the surface of the current collector and contact areas of the graphene layers and the current collector are large and thus interactional forces are strong; falling off is difficult; adhesive forces are strong; separation of the active material and the current collector is avoided in charging and discharging; and internal resistance reduction is promoted.
Description
Technical field
The present invention relates to the lithium secondary battery field, relate in particular to a kind of collector and preparation method thereof.
Background technology
Lithium secondary battery in the small portable electronic product, obtained being widely used, and its application prospect in high power electrokinetic cell and big capacity energy-storage battery has more attracted global sight as a kind of high power capacity, long-life energy-storage system.The research and development of high performance lithium ion battery are vital tasks in electrochemical energy storage field.
In lithium secondary battery, active material is evenly coated aluminium foil or Copper Foil collection liquid surface, and collector is through contacting the electronics that electrochemical reaction is produced and compile and export to external circuit with the physics of active material, thereby realizes that chemical energy is converted into the process of electric energy.Can know by inference thus, contacting between collector and active material is the important factor in order of lithium ion battery charge-discharge performance.
In the conventional at present lithium secondary battery pole piece manufacture craft, active material slurry is directly coated aluminium foil or copper foil surface, and dry back realizes that through binding agent active material is fixed in collection liquid surface.Yet; There is the defective of following two aspects in such structural design: 1) metal collector of rigidity and the contact area between active material particle are limited; Interface resistance is bigger, causes the rising of the internal resistance of cell, for battery performance particularly the performance under the high current charge-discharge condition have negative effect; 2) adhesion strength of binding agent is limited, and in the charge and discharge process that continues, the expansion that is easy to take place between active material and collector breaks away from, and causes the internal resistance of cell further to strengthen, and makes the security performance of cycle life and battery be affected.Therefore, reduce the interface resistance between collector and active material, the adhesion strength that improves between the two is the important means that promotes the lithium secondary battery performance.
It is the main path that realizes above-mentioned target that collector is carried out surface treatment.Reported method mainly contains two kinds at present, and a kind of is through the method for chemistry or physics collector to be carried out surface etch, forms concavo-convex not clear rough surface, thereby improves the contact area of collector and active material, and strengthens adhesive force.But this method and technology technological requirement is higher, and cost is comparatively expensive, is unfavorable for producing on a large scale needs.Another kind method is to apply the thin layer that contains electric conducting material at collection liquid surface; This thin layer needs favorable conductive ability, higher specific surface area, high adhesive property; And has better deformability with respect to metal collector; Contact with conduction between collector thereby increase active material, reduce interface resistance, and raising adhesion strength between the two.This method can be utilized the conventional battery coating apparatus simultaneously, and is easy and simple to handle, with low cost, is an important development direction of collection liquid surface modification.
In above-mentioned conductive coating, the selection of electric conducting material is undoubtedly most important link.Take all factors into consideration the selection that material with carbon element is best suited for from electric conductivity and cost.Material with carbon element is of a great variety, and common have graphite, carbon black, CNT and a carbon fiber etc.But because graphite or carbon black are three-dimensional structures, graphite or carbon black constitute the some contact with contacting of Copper Foil, thereby make the conductive coating of formation not fine and close, are prone to come off, and influence interface resistance and adhesion strength to a certain extent, finally influence the performance of battery.
Summary of the invention
The technical problem that the present invention solves is to provide a kind of secondary cell collector; Coating modified through collection liquid surface being carried out Graphene; Reduced the contact resistance between collector and active material, improved cohesive force between the two, the final comprehensive lifting that realizes battery performance.
The invention discloses a kind of collector, comprise the collector foil, said collector foil has the coating of graphitiferous alkene and binding agent on the one side at least.
The invention also discloses a kind of preparation method of collector, comprising:
Graphene and binding agent are disperseed in solvent, form slurry; Said slurry coating at least one surface of collector foil, is formed the coating that contains Graphene and binding agent; Carry out drying then.
Preferably, the mass ratio of said Graphene and binding agent is (1～49): 1.
Preferably, the number of plies of said Graphene is an individual layer or between 1～30 layer; Carbon content＞the 95wt% of said Graphene, the body conductance＞100S/cm of said Graphene.
Preferably, the method for said dispersion be stirring, high speed shear, emulsification and ultrasonic in one or more.
Preferably, said solvent is water, water and ethanol mixed solvent or N-methyl pyrrolidone.
Preferably, also comprise after the said step that Graphene and binding agent are disperseed in solvent: deaeration is handled and is sieved.
Preferably, said solid content of slurry is 0.2～20wt%, and the viscosity of said slurry is 50～5000mPas.
Preferably, the thickness of said coating is 0.005～10 micron.
Preferably, said coating is 30%～100% in the coverage rate on collector foil surface.
Preferably, said coating also comprises one or more in graphite, carbon black, acetylene black, CNT, the carbon fiber.
The invention provides a kind of preparation method of collector, compared with prior art, the collection liquid surface of preparing according to method provided by the invention has the coating of graphitiferous alkene and binding agent.The graphene conductive performance is very excellent in the coating, and its conductivity can reach 10
6S/cm can strengthen the conductivity between collector and the active material, reduces the internal resistance of battery; Simultaneously because exclusive two-dimentional laminar structured of Graphene; Make Graphene form even, fine and close coating on collector foil surface; Improved Graphene greatly in collector foil surface contact area; Increase active material and contact, can reduce the interface resistance between collector and the active material effectively, the reduction internal resistance with conduction between the collector; Be tiled between the Graphene lamella of collection liquid surface and and the collector foil between contact area big; Interaction force is strong; Difficult drop-off, adhesion strength is strong, and the disengaging between active material and collector can not take place in charging and discharging process; Help reducing internal resistance, thereby improve the performance of battery comprehensively.
Description of drawings
Fig. 1 is the structural representation of the collector of the embodiment of the invention 1 preparation;
Fig. 2 is the sem photograph of the collector of the embodiment of the invention 1 preparation;
Fig. 3 is the AC impedance spectrogram before and after the test of battery high magnification;
Fig. 4 is the internal resistance variation diagram of battery in different phase;
Fig. 5 is the discharge curve of battery under the 5C multiplying power;
Fig. 6 is battery battery surface temperature variations when under the 5C multiplying power, discharging;
Fig. 7 is the discharge curve of battery in the time of-20 ℃.
Embodiment
In order further to understand the present invention, below in conjunction with embodiment the preferred embodiment of the invention is described, describe just to further specifying feature and advantage of the present invention but should be appreciated that these, rather than to the restriction of claim of the present invention.
The embodiment of the invention discloses a kind of secondary cell collector, comprise the collector foil, said collector foil has the coating of graphitiferous alkene and binding agent on the one side at least.Said collector foil is preferably Copper Foil or aluminium foil.
As preferred version, the content of Graphene is 50wt%～98wt% in the said coating.The effect of binding agent in coating be make Graphene can firm attachment on collector, be unlikely in use to come off.Binding agent is originally as insulator, and addition can influence the conductivity of Graphene coating.Therefore, the addition of binding agent is preferably 2wt%～50wt%, too much can cause the collector too high in resistance, and I haven't seen you for ages excessively influences the adhesion strength of Graphene coating.Said binding agent is preferably one or more in sodium carboxymethylcellulose, Kynoar, polytetrafluoroethylene, butadiene-styrene rubber and the LA series binding agent.
The present invention also provides a kind of preparation method of secondary cell collector, comprising: Graphene and binding agent are disperseed in solvent, form slurry; Said slurry coating at least one surface of collector foil, is formed the coating that contains Graphene and binding agent; Carry out drying then.
In order to make coating have good electrical conductivity, as preferred version, the mass ratio of above-mentioned Graphene and binding agent is (1～49): 1; The number of plies of said Graphene is preferably between individual layer or 1～30 layer, is sp in the layer
2Carbon atom six sides of hydridization are tightly packed, the coating carbon material that interlayer combines with the π key; Carbon content＞the 95wt% of Graphene, bulk conductivity＞100S/cm.Said binding agent is preferably one or more in sodium carboxymethylcellulose, Kynoar, polytetrafluoroethylene, butadiene-styrene rubber and the LA series binding agent.
In the preparation method of collector, the method for above-mentioned dispersion is preferably stirring, high speed shear, emulsification, in ultrasonic one or more.In order to make in the coating Graphene and binding agent more tiny evenly, as preferred version, also comprise after the above-mentioned step that Graphene and binding agent are disperseed in solvent: deaeration is handled and is sieved, thereby guarantees the coating of formation even compact on the collector foil.According to the present invention, above-mentioned slurry can apply through coating process, and said coating process is preferably coating machine coating, casting, dip coating or printing.Continuous or discrete application pattern can be preferably adopted in said coating.The temperature of above-mentioned drying is preferably 30～200 ℃.As preferred version, said drying can be right after coating process carries out synchronously, also can be dry in the lump after coating finishes.
In the preparation method, said solvent is preferably water, water and ethanol mixed solvent or n-formyl sarcolysine base pyrrolidones, and the mass ratio of water and ethanol is preferably (20～400) in said water and the alcohol mixed solvent: 1, more preferably (50～300): 1.Said solid content of slurry is preferably 0.2～20wt%; The viscosity of said slurry is preferably 50～5000mPas; 500～1000mPas more preferably; The viscosity of slurry too little or too big city influence the coating or the printing performance of slurry, the uniformity of coating and continuity are affected, even can't be coated with or print.In order to make coating have better conductivity, the present invention also can add other electric conducting materials in solvent, is preferably in graphite, carbon black, acetylene black, CNT, the carbon fiber one or more.
According to the present invention, coating is as the non-active material in the electrode, and itself can reduce the energy density of battery along with the increase of coating layer thickness on the contrary for the not contribution of capacity of battery, and therefore, in theory, coating is to get over Bao Yuehao.But, might adverse effect be arranged to its performance along with the coating attenuate.For the material with carbon element of routine, the scope of conductive coating is usually at one micron to tens microns.And for Graphene, because the distinguished two-dimensional structure of Graphene even its thickness has only tens to the hundreds of nanometer, can both play good effect, the thickness of coating of the present invention is preferably 0.005～10 micron, more preferably 0.1～5 micron.Coating is preferably 30%～100% in the coverage rate on collector foil surface.
The present invention has prepared the secondary cell collector, and at least one mask of the collector foil of preparation has the coating of graphitiferous alkene and binding agent, because the electric conductivity of Graphene is excellent; Greatly strengthened the conductivity between collector and active material, the exclusive two-dimensional structure of Graphene makes Graphene can form the coating of even compact on collector foil surface simultaneously; Having increased collector contacts with conduction between active material; Reduced interface resistance, and be tiled between the Graphene lamella on collector foil surface and and the collector foil between contact area big, interaction force is strong; Difficult drop-off, adhesion strength is strong.Therefore can improve the performance of battery effectively through the coating that has Graphene in collector foil surface applied.
In order further to understand the present invention, below in conjunction with embodiment the preparation method of collector provided by the invention is described in detail, protection scope of the present invention is not limited by the following examples.
Taking by weighing the 2g sodium carboxymethylcellulose joins in the 1000g deionized water; The employing mixer mixes, and then adding 40g Graphene slurry mixes graphitiferous alkene 8g in the Graphene slurry; Add the 2000g deionized water and regulate slurry viscosity; Viscosity Control is 800mPas, adds 30g ethanol at last and carries out low speed vacuum stirring deaeration processing, crosses 150 eye mesh screens and obtains slurry; This slurry is coated on aluminium foil surface uniformly through the transfer type coating machine, and in air dry oven, dries, obtaining the single face coating layer thickness is the graphene conductive coating of 500 nanometers.
Adopting the peeling strength test machine to record peel strength above-mentioned prepared collector is 0.5N, and adopting the resistivity of four probe method test pole piece is 4.553E
-6Ohm.cm.
Fig. 1 is the structural representation of the collector of embodiment 1 preparation, and this sketch map comprises tinsel 1 and be overlying on said tinsel 1 coating surfaces 2 that coating comprises Graphene and binding agent.
Collection liquid surface to present embodiment preparation scans, and Fig. 2 is the sem photograph of graphene conductive coating, as can be seen from the figure, and the densification that on the collector foil, is evenly distributed of graphene conductive coating.
Taking by weighing the 1.5g sodium carboxymethylcellulose joins in the 1000g deionized water; The employing mixer mixes, and then adds 30g Graphene slurry and 0.5g conductive carbon black (Super P) mixes, and contains the 8g Graphene in the Graphene slurry; Add the 2000g deionized water and regulate slurry viscosity; Viscosity Control is 600mPas, adds 30g ethanol at last and carries out low speed vacuum stirring deaeration processing, crosses 150 eye mesh screens and obtains slurry; This slurry is coated on aluminium foil surface uniformly through the transfer type coating machine, and in air dry oven, dries, obtaining the single face coating layer thickness is the graphene conductive coating of 200 nanometers.
Adopting the peeling strength test machine to record peel strength above-mentioned prepared collector is 0.5N, and adopting the resistivity of four probe method test pole piece is 4.761E
-6Ohm.cm.
Embodiment 3
Take by weighing the 8g graphene powder and join in the 500g n-formyl sarcolysine base pyrrolidones and to soak 8 hours, ultrasonic dispersion 10 minutes, supersonic frequency is 15KHz; Taking by weighing the 2g Kynoar joins in the 1000g n-formyl sarcolysine base pyrrolidones; The employing mixer mixes; And then the Graphene slurry mixes after adding the ultrasonic dispersion of 508g; Add 1500g n-formyl sarcolysine base pyrrolidones then and regulate slurry viscosity, viscosity Control is 1000mPas, crosses 150 eye mesh screens and obtains slurry; This slurry is coated on aluminium foil surface uniformly through the transfer type coating machine, and in air dry oven, dries, obtaining the single face coating layer thickness is the graphene conductive coating of 200 nanometers.
Adopting the peeling strength test machine to record peel strength above-mentioned prepared collector is 0.25N, and adopting the resistivity of four probe method test pole piece is 5.653E
-6Ohm.cm.
Embodiment 4
Take by weighing the 8g graphene powder and join in the 500g n-formyl sarcolysine base pyrrolidones and to soak 8 hours, ultrasonic then dispersion 10 minutes, supersonic frequency is 15KHz; Taking by weighing the 1.5g Kynoar adds in the 1000g n-formyl sarcolysine base pyrrolidones; The employing mixer mixes; Add 0.5g SP and mix, and then the 508g Graphene slurry that adds after the ultrasonic dispersion mixes adding 1500g n-formyl sarcolysine base pyrrolidones adjusting slurry viscosity; Viscosity Control is 1000mPas, crosses 150 eye mesh screens and obtains slurry; This slurry is coated on aluminium foil surface uniformly through the transfer type coating machine, and in air dry oven, dries, obtaining the single face coating layer thickness is the graphene conductive coating of 500 nanometers.
Adopting the peeling strength test machine to record peel strength above-mentioned prepared collector is 0.25N, and adopting the resistivity of four probe method test pole piece is 5.362E
-6Ohm.cm.
Taking by weighing 53.3g LA133 (solid content is 15%) joins in the 1100g deionized water; The employing mixer mixes, and then adds 40g Graphene slurry and mix, and contains the 8g Graphene in the Graphene slurry; Add the 1900g deionized water and regulate slurry viscosity; Viscosity Control is 800mPas, adds 30g ethanol at last and carries out low speed vacuum stirring deaeration processing, crosses 150 eye mesh screens and obtains slurry; This slurry is coated on aluminium foil surface uniformly through the transfer type coating machine, and in air dry oven, dries, obtaining the single face coating layer thickness is the graphene conductive coating of 100 nanometers.
Adopting the peeling strength test machine to record peel strength above-mentioned prepared collector is 0.6N, and adopting the resistivity of four probe method test pole piece is 4.453E
-6Ohm.cm.
Taking by weighing the 2g sodium carboxymethylcellulose joins in the 1000g deionized water; The employing mixer mixes, and then adds 40g Graphene slurry and mix, and contains the 8g Graphene in the Graphene slurry; Add the 2000g deionized water and regulate slurry viscosity; Viscosity Control is 800mPas, adds 30g ethanol at last and carries out low speed vacuum stirring deaeration processing, crosses 150 eye mesh screens and obtains slurry; This slurry is coated on copper foil surface uniformly through the transfer type coating machine, and in air dry oven, dries, obtaining the single face coating layer thickness is the graphene conductive coating of 200 nanometers.
Adopting the peeling strength test machine to record peel strength above-mentioned prepared collector is 0.5N, and adopting the resistivity of four probe method test pole piece is 1.353E
-6Ohm.cm.
Embodiment 7
Taking by weighing the 2g sodium carboxymethylcellulose joins in the 1000g deionized water; The employing mixer mixes, and then adds 40g Graphene slurry and mix, and contains the Graphene of 8g in the Graphene slurry; Add the 2000g deionized water and regulate slurry viscosity; Viscosity Control is 200mPas, adds 30g ethanol at last and carries out low speed vacuum stirring deaeration processing, crosses 150 eye mesh screens and obtains slurry; This slurry is coated on aluminium foil surface uniformly through screen process press, and in air dry oven, dries, obtaining the single face coating layer thickness is 200 nanometers, and is the graphene conductive coating of discontinuous gridding, and the Graphene coating is 50% in the coverage rate of aluminium foil surface.
Adopting the peeling strength test machine to record peel strength above-mentioned prepared collector is 0.5N, and adopting the resistivity of four probe method test pole piece is 3.632E
-6Ohm.cm.
Taking by weighing the 2g sodium carboxymethylcellulose joins in the 1000g deionized water; The employing mixer mixes, and then adds 40g Graphene slurry and mix, and contains the 8g Graphene in the Graphene slurry; Add the 2000g deionized water and regulate slurry viscosity; Viscosity Control is 200mPas, adds 30g ethanol at last and carries out low speed vacuum stirring deaeration processing, crosses 150 eye mesh screens and obtains slurry; This slurry is coated on aluminium foil surface uniformly through extrusion coater, and in air dry oven, dries, obtaining the single face coating layer thickness is the graphene conductive coating of 100 nanometers.
Adopting the peeling strength test machine to record peel strength above-mentioned prepared collector is 0.5N, and adopting the resistivity of four probe method test pole piece is 4.372E
-6Ohm.cm.
Comparative example 1
The tinsel that employing is buied from market is as collector, and tinsel is an aluminium foil.
Adopt the collector of embodiment 1 to prepare 18650 column type power lithium-ion batteries, be numbered: battery 1; Adopt the collector of Comparative Examples 1 to prepare lithium ion battery simultaneously, be numbered: battery 2.Test the ac impedance spectroscopy of above-mentioned two kinds of battery high magnifications front and back; Test result is as shown in Figure 3; Fig. 3 is the AC impedance spectrogram of battery 1 and battery 2 high magnifications test front and back, and the ■ curve is the AC impedance spectral curve before the test of battery 2 high magnifications among Fig. 3, ● curve is the AC impedance spectral curve after the test of battery 2 high magnifications; ▲ curve is the AC impedance spectral curve before the test of battery 1 high magnification; The ★ curve is the AC impedance spectral curve after the test of battery 1 high magnification, and as can beappreciated from fig. 3, the internal resistance of battery 1 will be lower than the internal resistance of battery 2.
The internal resistance of battery 1 and battery 2 is tested; Test result is as shown in Figure 4, and Fig. 4 is battery 1 and the internal resistance variation diagram of battery 2 in different phase, and the ■ curve is the internal resistance change curve of battery 2 among Fig. 4; ▲ curve is the internal resistance change curve of battery 1; As can beappreciated from fig. 4, the internal resistance of battery 1 reduces by 10%～50% than the internal resistance of battery 2, and the internal resistance of battery 1 changes more steady.
Voltage when battery 1 and battery 2 are discharged under the 5C multiplying power is tested; Test result is as shown in Figure 5; Fig. 5 is battery 1 and the discharge curve of battery 2 under the 5C multiplying power, and curve a is the discharge curve of battery 1 under the 5C multiplying power, and curve b is the discharge curve of battery 2 under the 5C multiplying power; As can beappreciated from fig. 5, battery 1 improves 0.1～0.2V than pressing in the discharge of battery 2 under the 5C multiplying power.
The surface temperature variation that battery 1 and battery 2 discharge under the 5C multiplying power is tested; Test result is as shown in Figure 6; Fig. 6 is battery 1 a battery surface variations in temperature when discharging under the 5C multiplying power with battery 2, and curve a is the surface temperature change curve that battery 2 discharges under the 5C multiplying power among Fig. 6, and curve b is the surface temperature change curve that battery 1 discharges under the 5C multiplying power; Surface temperature when as can beappreciated from fig. 6, battery 1 discharges under the 5C multiplying power than battery 2 fully reduces more than 20 ℃.
Can know from above test result, adopt in the battery use of collector preparation of the present invention, for the battery that adopts conventional collector preparation; Internal resistance stability better; Reduced internal resistance, strengthened cyclical stability, the performance of battery is improved.
The explanation of above embodiment just is used for helping to understand method of the present invention and core concept thereof.Should be pointed out that for those skilled in the art, under the prerequisite that does not break away from the principle of the invention, can also carry out some improvement and modification to the present invention, these improvement and modification also fall in the protection range of claim of the present invention.
To the above-mentioned explanation of the disclosed embodiments, make this area professional and technical personnel can realize or use the present invention.Multiple modification to these embodiment will be conspicuous concerning those skilled in the art, and defined General Principle can realize under the situation that does not break away from the spirit or scope of the present invention in other embodiments among this paper.Therefore, the present invention will can not be restricted to these embodiment shown in this paper, but will meet and principle disclosed herein and features of novelty the wideest corresponding to scope.
Claims (11)
1. a collector comprises the collector foil, it is characterized in that, said collector foil has the coating of graphitiferous alkene and binding agent on the one side at least.
2. the preparation method of a collector is characterized in that, comprising:
Graphene and binding agent are disperseed in solvent, form slurry; Said slurry coating at least one surface of collector foil, is formed the coating that contains Graphene and binding agent; Carry out drying then.
3. preparation method according to claim 2 is characterized in that, the mass ratio of said Graphene and binding agent is (1～49): 1.
4. preparation method according to claim 2 is characterized in that, the number of plies of said Graphene is between individual layer or 1～30 layer; Carbon content＞the 95wt% of said Graphene, the bulk conductivity＞100S/cm of said Graphene.
5. preparation method according to claim 2 is characterized in that, the method for said dispersion be stirring, high speed shear, emulsification and ultrasonic in one or more.
6. preparation method according to claim 2 is characterized in that, said solvent is water, water and ethanol mixed solvent or N-methyl pyrrolidone.
7. preparation method according to claim 2 is characterized in that, also comprise after the said step that Graphene and binding agent are disperseed in solvent: deaeration is handled and sieved.
8. manufacturing approach according to claim 2 is characterized in that, said solid content of slurry is 0.2～20wt%, and the viscosity of said slurry is 50～5000mPas.
9. preparation method according to claim 2 is characterized in that, the thickness of said coating is 0.005～10 micron.
10. preparation method according to claim 2 is characterized in that, said coating is 30%～100% in the coverage rate on collector foil surface.
11. preparation method according to claim 2 is characterized in that, said coating also comprises one or more in graphite, carbon black, acetylene black, CNT, the carbon fiber.
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