CN111477870A - Composition, preparation method and application of composition in conductive paste - Google Patents

Composition, preparation method and application of composition in conductive paste Download PDF

Info

Publication number
CN111477870A
CN111477870A CN201911305394.0A CN201911305394A CN111477870A CN 111477870 A CN111477870 A CN 111477870A CN 201911305394 A CN201911305394 A CN 201911305394A CN 111477870 A CN111477870 A CN 111477870A
Authority
CN
China
Prior art keywords
dispersant
composition
agent
graphite
preparation
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.)
Pending
Application number
CN201911305394.0A
Other languages
Chinese (zh)
Inventor
王建兴
刘才超
魏鹏亮
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Guangdong Yina Technology Co ltd
Original Assignee
Guangdong Yina Technology Co ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Guangdong Yina Technology Co ltd filed Critical Guangdong Yina Technology Co ltd
Priority to CN201911305394.0A priority Critical patent/CN111477870A/en
Publication of CN111477870A publication Critical patent/CN111477870A/en
Pending legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/62Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H01M4/624Electric conductive fillers
    • H01M4/625Carbon or graphite
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/04Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of carbon-silicon compounds, carbon or silicon
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Abstract

The invention belongs to the field of research and development of battery products, and particularly relates to a composition, a preparation method and application of the composition in conductive paste. The present invention provides a composition comprising: a dispersant and a carbon material; the carbon material is selected from: any one or more of expanded graphite, flake graphite, crystalline graphite, cryptocrystalline graphite, carbon fiber, pyrolytic carbon, foam graphite, and ketjen black. The invention provides a preparation method of the composition, and application of the composition or a product obtained by the preparation method in conductive paste. According to the invention, the aqueous graphene conductive slurry is directly prepared by a physical stripping method, so that the preparation cost and time are effectively saved, and simultaneously, the graphene can be uniformly and stably dispersed in the solvent; the technical defects that in the prior art, the graphite emulsion in the battery is difficult to give consideration to good conductivity, corrosion resistance, adhesive force and small pollution are overcome.

Description

Composition, preparation method and application of composition in conductive paste
Technical Field
The invention belongs to the field of research and development of battery products, and particularly relates to a composition, a preparation method and application of the composition in conductive paste.
Background
With the advance of technology and the rapid development of economy, more and more electronic products are produced, which require a large amount of chemical power sources, and the common chemical power sources include: alkaline batteries, carbon batteries, lithium iron batteries, lead storage batteries, lithium ion batteries, and the like. Most of the positive and negative active materials of the battery are directly placed in the metal shell through the metal current collectors, and the contact with the metal can cause the phenomena of large internal resistance of the battery and corrosion of the shell.
The alkaline zinc-manganese battery has small internal resistance, low self-discharge during storage and MnO 2 The high-efficiency energy-saving battery has the excellent performances of high utilization rate, repeated charging and the like, and is a commonly used energy supply battery for large-current working equipment used in daily life. The alkaline battery comprises a steel shell, a positive electrode, a negative electrode, a diaphragm and electrolyte; the steel shell is a container for loading chemical active substances, and is also a current collector of the anode, so that in order to reduce the contact resistance between the steel shell and the anode ring and prevent the electrolyte from corroding the inner surface of the steel shell, a layer of conductive graphite emulsion is usually sprayed on the inner wall of the steel shell.
In the prior art, the graphite emulsion used in the battery is usually prepared from an organic solvent with strong volatility, so that the graphite emulsion has great harm to human bodies and the environment, is easy to pollute, and needs to be further improved in conductivity, corrosion resistance and adhesion.
Therefore, a composition, a preparation method and an application thereof in conductive paste are developed to solve the technical defects that in the prior art, graphite emulsion in a battery has difficulty in simultaneously achieving good conductivity, corrosion resistance, adhesion and small pollution, and thus the problem to be solved by the technical staff in the field is urgently needed.
Disclosure of Invention
In view of the above, the invention provides a composition, a preparation method and an application thereof in conductive paste, which are used for solving the technical defects that in the prior art, graphite emulsion in a battery is difficult to have good conductivity, corrosion resistance, adhesion and low pollution.
The invention provides a composition, which comprises the following raw materials: a dispersant and a carbon material;
the carbon material is selected from: any one or more of expanded graphite, flake graphite, crystalline graphite, cryptocrystalline graphite, carbon fiber, pyrolytic carbon, foam graphite, and ketjen black.
Preferably, the raw materials of the composition comprise the following components in parts by mass: 15-30 parts of dispersing agent and 50-100 parts of carbon material.
Preferably, the dispersant is selected from: any one or more of an anionic wetting dispersant, a cationic wetting dispersant and a non-ionic wetting dispersant.
Preferably, the anionic wetting dispersant is selected from: any one or more of carboxylate dispersant, sulfate dispersant, phosphate dispersant and sulfonate dispersant.
Preferably, the cationic wetting and dispersing agent is selected from: any one or more of amine salt dispersant, quaternary ammonium salt dispersant and pyridinium salt dispersant.
Preferably, the non-ionic wetting dispersant is selected from: any one or more of ethylene glycol dispersant, polyhydric alcohol dispersant and cellulose dispersant.
Preferably, the raw materials of the composition further comprise: an auxiliary agent;
the auxiliary agent is selected from: any one or more of an emulsifier, a defoaming agent, a wetting agent, a curing agent, a film forming agent, a leveling agent and a rheological agent.
The invention provides a preparation method of the composition, which comprises the following steps: dispersing after dissolving the dispersant in deionized water, mixing with carbon material and shearing to obtain the product.
Preferably, the preparation method further comprises the following steps: any one or more of homogenization, ball milling, sanding and ultrasonic dispersion;
the homogenizing, ball milling, sanding and ultrasonic dispersing are carried out after the shearing step.
The invention provides an application of the composition or the product obtained by the preparation method in conductive paste.
In summary, the present invention provides a composition, which comprises the following raw materials: a dispersant and a carbon material; the carbon material is selected from: any one or more of expanded graphite, flake graphite, crystalline graphite, cryptocrystalline graphite, carbon fiber, pyrolytic carbon, foam graphite, and ketjen black. The invention provides a preparation method of the composition, and application of the composition or a product obtained by the preparation method in conductive paste. According to the technical scheme provided by the invention, the aqueous graphene conductive slurry is directly prepared by a physical stripping method, so that the preparation cost and time are effectively saved, and simultaneously, the graphene can be uniformly and stably dispersed in the solvent; further, through detection, compared with a commercially available reference product, the product prepared by the technical scheme provided by the invention has good conductivity, corrosion resistance and water resistance, and has better adhesive force with a base material. The composition, the preparation method and the application of the composition in the conductive paste solve the technical defects that in the prior art, the graphite emulsion in the battery is difficult to give consideration to good conductivity, corrosion resistance, adhesive force and small pollution.
Detailed Description
The invention provides a composition, a preparation method and application thereof in conductive paste, which are used for solving the technical defects that in the prior art, the graphite emulsion in a battery is difficult to give consideration to good conductivity, corrosion resistance, adhesive force and small pollution.
The technical solutions in the embodiments of the present invention will be described clearly and completely below, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
In order to illustrate the present invention in more detail, a composition, a preparation method and an application thereof in conductive paste provided by the present invention are specifically described below with reference to examples.
Example 1
This example is a specific example of preparing a graphene conductive paste product 1.
Dissolving 15g of dispersing agent in 1L of deionized water, dispersing for 2h at the rotating speed of 500r/min, mixing with 5g of carbon material, and shearing for 3h at the rotating speed of 3000r/min to obtain the graphene conductive slurry product 1.
In this example, the carbon material was expanded graphite, and the dispersant was an anionic wetting dispersant phosphate dispersant.
In the embodiment, the whole preparation process is carried out in a room temperature environment, and a circulating cold water bath cooling mode can be adopted to cool the reaction system, so that agglomeration in the reaction system is prevented.
In the practical application process, any one or more of an emulsifier, a defoaming agent, a wetting agent, a curing agent, a film forming agent, a leveling agent and a rheological agent can be added into the raw materials according to specific individual requirements.
In the process of practical application, any one or more steps of homogenizing, ball milling, sanding and ultrasonic dispersion can be added after shearing according to the specific real-time shearing effect and the requirements of different application scenes, so that the preparation process is further optimized.
Example 2
This example is a specific example of preparing a graphene conductive paste product 2.
And after 20g of dispersing agent is dissolved in 1L of deionized water, dispersing for 2h at the rotating speed of 500r/min, mixing with 6g of carbon material, and shearing for 3h at the rotating speed of 3000r/min to obtain a graphene conductive slurry product 2.
In this example, the carbon material is flake graphite, and the dispersant is a mixture of an anionic wetting dispersant, a sulfate dispersant, and a sulfonate dispersant.
In the embodiment, the whole preparation process is carried out in a room temperature environment, and a circulating cold water bath cooling mode can be adopted to cool the reaction system, so that caking in the reaction system is prevented.
In the practical application process, any one or more of an emulsifier, a defoaming agent, a wetting agent, a curing agent, a film forming agent, a leveling agent and a rheological agent can be added into the raw materials according to specific individual requirements.
In the process of practical application, any one or more steps of homogenizing, ball milling, sanding and ultrasonic dispersion can be added after shearing according to the specific real-time shearing effect and the requirements of different application scenes, so that the preparation process is further optimized.
Example 3
This example is a specific example of preparing a graphene conductive paste product 3.
Dissolving 25g of dispersing agent in 1L of deionized water, dispersing for 2h at the rotating speed of 500r/min, mixing with 10g of carbon material, and shearing for 3h at the rotating speed of 3000r/min to obtain a graphene conductive slurry product 3.
In this embodiment, the carbon material is crystalline graphite, and the dispersant is an anionic wetting dispersant carboxylate dispersant.
In the embodiment, the whole preparation process is carried out in a room temperature environment, and a circulating cold water bath cooling mode can be adopted to cool the reaction system, so that caking in the reaction system is prevented.
In the practical application process, any one or more of an emulsifier, a defoaming agent, a wetting agent, a curing agent, a film forming agent, a leveling agent and a rheological agent can be added into the raw materials according to specific individual requirements.
In the process of practical application, any one or more steps of homogenizing, ball milling, sanding and ultrasonic dispersion can be added after shearing according to the specific real-time shearing effect and the requirements of different application scenes, so that the preparation process is further optimized.
Example 4
This example is a specific example of preparing a graphene conductive paste product 4.
And dissolving 30g of dispersing agent in 1L of deionized water, dispersing for 2h at the rotating speed of 500r/min, mixing with 8g of carbon material, and shearing for 3h at the rotating speed of 3000r/min to obtain a graphene conductive slurry product 4.
In this embodiment, the carbon material is cryptocrystalline graphite, and the dispersant is a cationic wetting dispersant amine salt dispersant.
In the embodiment, the whole preparation process is carried out in a room temperature environment, and a circulating cold water bath cooling mode can be adopted to cool the reaction system, so that caking in the reaction system is prevented.
In the practical application process, any one or more of an emulsifier, a defoaming agent, a wetting agent, a curing agent, a film forming agent, a leveling agent and a rheological agent can be added into the raw materials according to specific individual requirements.
In the process of practical application, any one or more steps of homogenizing, ball milling, sanding and ultrasonic dispersion can be added after shearing according to the specific real-time shearing effect and the requirements of different application scenes, so that the preparation process is further optimized.
Example 5
This example is a specific example of preparing a graphene conductive paste product 5.
Dissolving 18g of dispersing agent in 1L of deionized water, dispersing for 2h at the rotating speed of 500r/min, mixing with 7g of carbon material, and shearing for 3h at the rotating speed of 3000r/min to obtain the graphene conductive slurry product 5.
In this embodiment, the carbon material is carbon fiber, and the dispersant is a cationic wetting dispersant quaternary ammonium salt dispersant.
In the embodiment, the whole preparation process is carried out in a room temperature environment, and a circulating cold water bath cooling mode can be adopted to cool the reaction system, so that caking in the reaction system is prevented.
In the practical application process, any one or more of an emulsifier, a defoaming agent, a wetting agent, a curing agent, a film forming agent, a leveling agent and a rheological agent can be added into the raw materials according to specific individual requirements.
In the process of practical application, any one or more steps of homogenizing, ball milling, sanding and ultrasonic dispersion can be added after shearing according to the specific real-time shearing effect and the requirements of different application scenes, so that the preparation process is further optimized.
Example 6
This example is a specific example of preparing a graphene conductive paste product 6.
And dissolving 30g of dispersing agent in 1L of deionized water, dispersing for 2h at the rotating speed of 500r/min, mixing with 5g of carbon material, and shearing for 3h at the rotating speed of 3000r/min to obtain a graphene conductive slurry product 6.
In this embodiment, the carbon material is pyrolytic carbon, and the dispersant is a cationic wetting dispersant pyridinium salt dispersant.
In the embodiment, the whole preparation process is carried out in a room temperature environment, and a circulating cold water bath cooling mode can be adopted to cool the reaction system, so that caking in the reaction system is prevented.
In the practical application process, any one or more of an emulsifier, a defoaming agent, a wetting agent, a curing agent, a film forming agent, a leveling agent and a rheological agent can be added into the raw materials according to specific individual requirements.
In the practical application process, any one or more steps of homogenizing, ball milling, sanding and ultrasonic dispersion can be added after shearing according to the specific real-time shearing effect and the requirements on different application scenes, so that the preparation process is further optimized.
Example 7
This example is a specific example of preparing a graphene conductive paste product 7.
Dissolving 22g of dispersing agent in 1L of deionized water, dispersing for 2h at the rotating speed of 500r/min, mixing with 9g of carbon material, and shearing for 3h at the rotating speed of 3000r/min to obtain a graphene conductive slurry product 7.
In this example, the carbon material is graphite foam, and the dispersant is a non-ionic wetting dispersant, glycol dispersant.
In the embodiment, the whole preparation process is carried out in a room temperature environment, and a circulating cold water bath cooling mode can be adopted to cool the reaction system, so that caking in the reaction system is prevented.
In the practical application process, any one or more of an emulsifier, a defoaming agent, a wetting agent, a curing agent, a film forming agent, a leveling agent and a rheological agent can be added into the raw materials according to specific individual requirements.
In the process of practical application, any one or more steps of homogenizing, ball milling, sanding and ultrasonic dispersion can be added after shearing according to the specific real-time shearing effect and the requirements of different application scenes, so that the preparation process is further optimized.
Example 8
This example is a specific example of preparing a graphene conductive paste product 8.
Dissolving 25g of dispersing agent in 1L of deionized water, dispersing for 2h at the rotating speed of 500r/min, mixing with 10g of carbon material, and shearing for 3h at the rotating speed of 3000r/min to obtain a graphene conductive slurry product 8.
In this example, the carbon material was ketjen black, and the dispersant was a nonionic wetting dispersant, a polyol dispersant.
In the embodiment, the whole preparation process is carried out in a room temperature environment, and a circulating cold water bath cooling mode can be adopted to cool the reaction system, so that caking in the reaction system is prevented.
In the practical application process, any one or more of an emulsifier, a defoaming agent, a wetting agent, a curing agent, a film forming agent, a leveling agent and a rheological agent can be added into the raw materials according to specific individual requirements.
In the process of practical application, any one or more steps of homogenizing, ball milling, sanding and ultrasonic dispersion can be added after shearing according to the specific real-time shearing effect and the requirements of different application scenes, so that the preparation process is further optimized.
Example 9
This example is a specific example of preparing a graphene conductive paste product 9.
Dissolving 50g of dispersing agent in 3L of deionized water, dispersing for 2h at the rotating speed of 500r/min, mixing with 150g of carbon material, and shearing for 3h at the rotating speed of 3000r/min to obtain the graphene conductive slurry product 9.
In this example, the carbon material is expanded graphite, and the dispersant is a cellulose dispersant as a nonionic wetting dispersant.
In the embodiment, the whole preparation process is carried out in a room temperature environment, and a circulating cold water bath cooling mode can be adopted to cool the reaction system, so that caking in the reaction system is prevented.
In the practical application process, any one or more of an emulsifier, a defoaming agent, a wetting agent, a curing agent, a film forming agent, a leveling agent and a rheological agent can be added into the raw materials according to specific individual requirements.
In the process of practical application, any one or more steps of homogenizing, ball milling, sanding and ultrasonic dispersion can be added after shearing according to the specific real-time shearing effect and the requirements of different application scenes, so that the preparation process is further optimized.
Example 10
This example is a specific example for measuring the conductivity, corrosion resistance and adhesion of the graphene conductive paste products 1 to 10 prepared in examples 1 to 10. In this example, the control used was a commercially available homogeneous graphite emulsion.
10.1 measurement of conductivity
The prepared slurry is evenly spread on a PET film by scraping, the wet film thickness is 100 mu m, after the slurry is fully dried, the surface resistance is tested by adopting a four-probe method, and the average value is obtained by taking points for multiple times. The coating was 10cm long ﹡ cm wide.
10.2 determination of Corrosion resistance
The salt spray resistance test is carried out according to the regulation of GB/T1733-93.
10.3 determination of adhesion
The paint film adhesion is tested by adopting a cross-cut method according to the GB/T9286-1998 standard.
10.4 results of the experiment
The above measurement results are shown in Table 1.
TABLE 1
Figure BDA0002320343880000071
Figure BDA0002320343880000081
As can be seen from the table 1, compared with a reference substance, the product prepared by the technical scheme provided by the invention has good conductivity, water resistance, corrosion resistance and adhesive force; further combining with the embodiments 1 to 9, in the preparation process, high-pollution, high-toxicity and high-volatility raw materials are not used, the preparation process is simple and convenient, no pollution is generated, and the raw materials are low in price and easy to obtain, so that the method is suitable for large-scale popularization in the field.
In summary, the present invention provides a composition, which comprises the following raw materials: a dispersant and a carbon material; the carbon material is selected from: any one or more of expanded graphite, flake graphite, crystalline graphite, cryptocrystalline graphite, carbon fiber, pyrolytic carbon, foam graphite, and ketjen black. The invention provides a preparation method of the composition, and application of the composition or a product obtained by the preparation method in conductive paste. According to the technical scheme provided by the invention, the aqueous graphene conductive slurry is directly prepared by a physical stripping method, so that the preparation cost and time are effectively saved, and simultaneously, the graphene can be uniformly and stably dispersed in the solvent; further, through detection, compared with a commercially available reference product, the product prepared by the technical scheme provided by the invention has good conductivity, corrosion resistance and water resistance, and has better adhesive force with a base material. The composition, the preparation method and the application of the composition in the conductive paste solve the technical defects that in the prior art, the graphite emulsion in the battery is difficult to give consideration to good conductivity, corrosion resistance, adhesive force and small pollution.
The foregoing is only a preferred embodiment of the present invention, and it should be noted that, for those skilled in the art, various modifications and decorations can be made without departing from the principle of the present invention, and these modifications and decorations should also be regarded as the protection scope of the present invention.

Claims (10)

1. A composition, characterized in that the raw materials of the composition comprise: a dispersant and a carbon material;
the carbon material is selected from: any one or more of expanded graphite, flake graphite, crystalline graphite, cryptocrystalline graphite, carbon fiber, pyrolytic carbon, foam graphite, and ketjen black.
2. The composition according to claim 1, wherein the composition comprises the following raw materials in parts by mass: 15-30 parts of dispersing agent and 5-10 parts of carbon material.
3. Composition according to claim 1 or 2, characterized in that the dispersant is chosen from: any one or more of an anionic wetting dispersant, a cationic wetting dispersant and a non-ionic wetting dispersant.
4. The composition according to claim 3, wherein the anionic wetting dispersant is selected from the group consisting of: any one or more of carboxylate dispersant, sulfate dispersant, phosphate dispersant and sulfonate dispersant.
5. The composition according to claim 3, characterized in that the cationic wetting and dispersing agent is chosen from: any one or more of amine salt dispersant, quaternary ammonium salt dispersant and pyridinium salt dispersant.
6. The composition according to claim 3, wherein the non-ionic wetting dispersant is selected from the group consisting of: any one or more of glycol dispersants, polyhydric alcohol dispersants and cellulose dispersants.
7. The composition of claim 1, wherein the raw materials of the composition further comprise: an auxiliary agent;
the auxiliary agent is selected from: any one or more of an emulsifier, a defoaming agent, a wetting agent, a curing agent, a film forming agent, a leveling agent and a rheological agent.
8. A process for the preparation of a composition comprising any one of claims 1 to 7, wherein the process comprises: dispersing after dissolving the dispersant in deionized water, mixing with carbon material and shearing to obtain the product.
9. The production method according to claim 8, characterized by further comprising: any one or more of homogenization, ball milling, sanding and ultrasonic dispersion;
the homogenizing, ball milling, sanding and ultrasonic dispersing are carried out after the shearing step.
10. Use of a composition according to any one of claims 1 to 7 or a product obtained by the preparation method according to any one of claims 8 to 9 in an electroconductive paste.
CN201911305394.0A 2019-12-16 2019-12-16 Composition, preparation method and application of composition in conductive paste Pending CN111477870A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201911305394.0A CN111477870A (en) 2019-12-16 2019-12-16 Composition, preparation method and application of composition in conductive paste

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201911305394.0A CN111477870A (en) 2019-12-16 2019-12-16 Composition, preparation method and application of composition in conductive paste

Publications (1)

Publication Number Publication Date
CN111477870A true CN111477870A (en) 2020-07-31

Family

ID=71746228

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201911305394.0A Pending CN111477870A (en) 2019-12-16 2019-12-16 Composition, preparation method and application of composition in conductive paste

Country Status (1)

Country Link
CN (1) CN111477870A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114789998A (en) * 2021-11-01 2022-07-26 广东一纳科技有限公司 Negative electrode material, preparation method thereof and battery

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105110318A (en) * 2015-07-23 2015-12-02 深圳市国创新能源研究院 Graphene aqueous slurry, and preparation method thereof
CN109110750A (en) * 2018-09-30 2019-01-01 青岛岩海碳材料有限公司 The method for preparing graphene using expanded graphite
CN109928386A (en) * 2017-12-18 2019-06-25 深圳先进技术研究院 A kind of graphene aqueous dispersions and preparation method thereof
CN110564233A (en) * 2019-06-17 2019-12-13 山东欧铂新材料有限公司 Water-based graphene conductive coating and preparation method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105110318A (en) * 2015-07-23 2015-12-02 深圳市国创新能源研究院 Graphene aqueous slurry, and preparation method thereof
CN109928386A (en) * 2017-12-18 2019-06-25 深圳先进技术研究院 A kind of graphene aqueous dispersions and preparation method thereof
CN109110750A (en) * 2018-09-30 2019-01-01 青岛岩海碳材料有限公司 The method for preparing graphene using expanded graphite
CN110564233A (en) * 2019-06-17 2019-12-13 山东欧铂新材料有限公司 Water-based graphene conductive coating and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114789998A (en) * 2021-11-01 2022-07-26 广东一纳科技有限公司 Negative electrode material, preparation method thereof and battery
CN114789998B (en) * 2021-11-01 2024-03-19 广东一纳科技有限公司 Negative electrode material, preparation method thereof and battery

Similar Documents

Publication Publication Date Title
CN108598490B (en) Three-dimensional porous metal negative current collector and preparation method and application thereof
CN104966822A (en) Multilayer coated lithium titanate cathode material of lithium ion battery and preparation method of multilayer coated lithium titanate cathode material
CN110010863A (en) A kind of method of lithium ion battery negative material prelithiation
CN105742641A (en) Conductive coating and lithium-ion battery employing same
CN103682327B (en) Based on the lithium ion battery and preparation method thereof of the hollow porous nickel oxide composite material of N doping carbon-coating parcel
CN104091937A (en) Lithium titanate-coated surface-treated graphite negative electrode material, preparation method and application of negative electrode material
CN111668493A (en) Three-dimensional current collector for inhibiting dendritic crystal of lithium metal negative electrode and application of three-dimensional current collector in metal lithium battery
CN108807886A (en) Double-coating anode material for lithium-ion batteries LiNi0.6Co0.2Mn0.2O2And preparation method thereof
CN107611337B (en) Method for coating positive electrode of lithium ion power battery
CN103972466B (en) Positive pole of a kind of high-temperature lithium thionyl chloride battery and preparation method thereof
CN110010878A (en) The porous carbon coating Co of N doping3O4Composite nano materials, preparation method and applications
CN111471369A (en) Composition, preparation method and application of composition in field of chemical power supply
CN109103433A (en) A kind of nitrogen mixes carbon-coated lithium iron phosphate composite and preparation method thereof
CN102664247B (en) Method for preparing LiFePO4/SiC lithium battery positive plate by microwave heating
CN103427072A (en) In-situ carbon coating method for lithium iron phosphate
CN109037552A (en) A kind of preparation method of the diaphragm material for sodium-sulphur battery
CN102185154A (en) Nano ferric phosphate hollow sphere lithium ion battery and preparation method thereof
CN111477870A (en) Composition, preparation method and application of composition in conductive paste
CN114613933A (en) Porous CeO2Zinc cathode coating design and aqueous zinc ion battery
CN112103499B (en) Graphene-based negative electrode material and preparation method thereof
CN110085864A (en) The preparation method and application of potassium or based lithium-ion battery positive plate
CN105895878A (en) Lithium titanate modified material and preparation method thereof
CN101504981A (en) Lithium iron phosphate/carbon composite electrode material and preparation method thereof
CN103441274B (en) Method for preparing high-density high-power spherical lithium iron phosphate positive material
GB2622164A (en) Modified iron phosphate precursor, modified lithium iron phosphate, and preparation methods therefor

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication

Application publication date: 20200731

RJ01 Rejection of invention patent application after publication