CN113380971B - Composite negative electrode material of thin-film lithium ion battery and preparation method thereof - Google Patents

Composite negative electrode material of thin-film lithium ion battery and preparation method thereof Download PDF

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CN113380971B
CN113380971B CN202110631096.1A CN202110631096A CN113380971B CN 113380971 B CN113380971 B CN 113380971B CN 202110631096 A CN202110631096 A CN 202110631096A CN 113380971 B CN113380971 B CN 113380971B
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lithium ion
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film lithium
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CN113380971A (en
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吴显明
龙芮涞
陈上
吴贤文
石青峰
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Jishou University
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    • 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
    • H01M4/04Processes of manufacture in general
    • H01M4/0402Methods of deposition of the material
    • H01M4/0404Methods of deposition of the material by coating on electrode collectors
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/05Accumulators with non-aqueous electrolyte
    • H01M10/052Li-accumulators
    • H01M10/0525Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • 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
    • H01M4/04Processes of manufacture in general
    • H01M4/0471Processes of manufacture in general involving thermal treatment, e.g. firing, sintering, backing particulate active material, thermal decomposition, pyrolysis
    • 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
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/362Composites
    • 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
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/48Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/485Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
    • 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
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/58Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
    • H01M4/5825Oxygenated metallic salts or polyanionic structures, e.g. borates, phosphates, silicates, olivines
    • 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 provides a preparation method of a composite cathode material of a film lithium ion battery, which comprises the following steps: dissolving lithium salt, aluminum nitrate and a phosphorus-containing compound in a solvent, and then dripping a titanium organic compound to obtain a precursor solution; depositing the precursor solution on a substrate, and carrying out heat treatment on the substrate at the temperature of 400-450 ℃ for 10-12 minutes to obtain a material matrix; soaking the material matrix in 0.2-0.3mol/L silver nitrate solution for 1-5 minutes, taking out, and then performing heat treatment at 700-850 ℃ for 2-30 minutes to obtain a material intermediate, wherein the content of silver element in the material intermediate is 0.5-5%; and (3) evaporating a 1-3 mu m Mo layer on the surface of the intermediate material to obtain the thin-film lithium ion battery composite negative electrode material. The invention also provides a composite cathode material of the film lithium ion battery. The composite negative electrode material of the film lithium ion battery provided by the invention has small internal resistance.

Description

Composite negative electrode material of thin-film lithium ion battery and preparation method thereof
[ technical field ] A method for producing a semiconductor device
The invention relates to the technical field of lithium ion batteries, in particular to a thin-film lithium ion battery composite negative electrode material and a preparation method thereof.
[ background ] A method for producing a semiconductor device
The lithium ion battery has the advantages of high energy density, long cycle life, stable working voltage, low self-discharge, no memory effect, small pollution and the like, so that the lithium ion battery is rapidly developed and widely applied and becomes a secondary battery with the most extensive application. The all-solid-state thin-film lithium ion battery is used as a branch of the lithium ion battery, all components in the battery structure exist in a solid state form and are formed by overlapping compact positive electrode films, electrolyte films and negative electrode films on a substrate, the all-solid-state thin-film lithium ion battery has extremely high safety, the solid electrolyte of the all-solid-state thin-film lithium ion battery is nonflammable, non-corrosive, non-volatile and liquid-tight, meanwhile, the dendritic lithium phenomenon is overcome, and the spontaneous combustion probability of an automobile carrying the all-solid-state lithium battery is greatly reduced.
In the related art, the thin film lithium ion battery has large internal resistance (more prominent when the thickness of an electrode thin film is increased), which hinders the application and development of the thin film battery. The internal resistance of the thin-film battery depends on the resistance of the positive and negative thin films to a great extent, and the reason for the large resistance of the positive and negative thin films mainly includes two points: compared with the conventional lithium ion battery electrode, the carbon black electronic conductive agent is lacked in the positive electrode and the negative electrode of the thin film battery, so that the electronic conductivity of the electrode thin film is lower; on the other hand, the thin film battery uses a solid electrolyte, which cannot be impregnated into the electrode as a liquid electrolyte, resulting in a low ionic conductivity of the electrode thin film. Therefore, it is necessary to provide a composite negative electrode material for a thin film lithium ion battery and a preparation method thereof to solve the above problems.
[ summary of the invention ]
The invention discloses a composite cathode material of a thin film lithium ion battery and a preparation method thereof, which aim to reduce the internal resistance of the thin film battery.
In order to achieve the purpose, the technical scheme of the invention is as follows:
a preparation method of a composite cathode material of a thin-film lithium ion battery comprises the following steps:
s1: dissolving lithium salt, aluminum nitrate and phosphorus-containing compound in solvent, and then dripping titanium organic compound to obtain Li 4 Ti 5 O 12 /Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 Precursor solution of the Li 4 Ti 5 O 12 /Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 The ratio of the amount of lithium, aluminum, titanium and phosphorus in the precursor solution is (3.53-3.953): (0.03-0.003): 4.42-4.942): 0.3-0.03;
s2: the Li is subjected to spray pyrolysis or spin coating technology 4 Ti 5 O 12 /Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 Depositing the precursor solution on a substrate, and performing heat treatment on the substrate at the temperature of 400-450 ℃ for 10-12 minutes to obtain a material matrix;
s3: soaking the material matrix in 0.2-0.3mol/L silver nitrate solution for 1-5 minutes, taking out, and then placing at 700-850 ℃ for heat treatment for 2-30 minutes to obtain a material intermediate, wherein the content of silver element in the material intermediate is 0.5-5%;
s4: and (3) evaporating a 1-3 mu m Mo layer on the surface of the intermediate material to obtain the thin-film lithium ion battery composite negative electrode material.
Preferably, the solvent is ethanol or ethylene glycol methyl ether.
Preferably, the lithium salt is lithium acetate or lithium nitrate.
Preferably, the titanium organic compound is a titanate.
Preferably, the titanium organic compound is tetrabutyl titanate or isopropyl titanate.
Preferably, the phosphorus-containing compound is ammonium dihydrogen phosphate, trimethyl phosphate, triethyl phosphate, tripropyl phosphate or tributyl phosphate.
Preferably, the substrate is a silicon wafer, a platinized silicon wafer or a lithium ion solid electrolyte Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 And sintering the sheet.
The invention also provides a film lithium ion battery composite negative electrode material prepared by the preparation method.
Preferably, the thickness of the composite negative electrode material of the thin-film lithium ion battery is less than 100 μm.
Compared with the prior art, the Li can be obtained by adopting soluble lithium salt, aluminum nitrate, titanium organic compound and phosphorus-containing compound as raw materials in proper proportion and controlling the synthesis conditions 4 Ti 5 O 12 /Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 And finally, plating a Mo/Ag composite plating layer on the material matrix. Due to Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 Is an excellent lithium ion conductor, the Mo/Ag composite coating is an excellent electronic conductor, and the prepared Li 4 Ti 5 O 12 The thin film contains Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 And the Mo/Ag composite coating can improve Li at the same time 4 Ti 5 O 12 Film(s)Ionic and electronic conductivity of, reducing Li 4 Ti 5 O 12 The film resistance is beneficial to preparing the low-resistance film lithium ion battery.
[ detailed description ] embodiments
The following detailed description of the present invention is provided to enable those skilled in the art to better understand the technical solutions in the embodiments of the present invention and to make the above objects, features and advantages of the present invention more comprehensible.
The invention provides a preparation method of a composite cathode material of a film lithium ion battery, which comprises the following steps:
s1: dissolving lithium salt, aluminum nitrate and phosphorus-containing compound in solvent, and then dripping organic titanium compound to obtain Li 4 Ti 5 O 12 /Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 Precursor solution of the Li 4 Ti 5 O 12 /Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 The ratio of the amount of lithium, aluminum, titanium and phosphorus in the precursor solution is (3.53-3.953): (0.03-0.003): 4.42-4.942): 0.3-0.03.
Lithium and titanium can react to form Li 4 Ti 5 O 12 And Li, al, ti and P may react to form Li 1.3 Al 0.3 Ti 1.7 (PO 4)3 Therefore, by appropriately controlling the amount ratio of lithium, aluminum, titanium, and phosphorus and the reaction conditions, li can be produced simultaneously 4 Ti 5 O 12 With Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 ,Li 4 Ti 5 O 12 As a negative electrode material of a lithium ion battery, can be mixed with LiMn 2 O 4 、LiCoO 2 And the 4V-grade anode material is used for forming the lithium ion battery with the working voltage of 2.4V. Li 4 Ti 5 O 12 The intercalation and deintercalation of lithium ions in the process of charging and discharging have little influence on the material structure, are called zero-strain materials, and are ideal cathode materials of solid film lithium ion batteries.
Preferably, the solvent is ethanol or ethylene glycol methyl ether; the lithium salt isLithium acetate or nitrate; the titanium organic compound is titanate; the titanium organic compound is tetrabutyl titanate or isopropyl titanate; the phosphorus-containing compound is ammonium dihydrogen phosphate, trimethyl phosphate, triethyl phosphate, tripropyl phosphate or tributyl phosphate; the substrate is a silicon wafer, a platinized silicon wafer or a lithium ion solid electrolyte Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 And sintering the sheet.
S2: the Li is subjected to spray pyrolysis or spin coating technology 4 Ti 5 O 12 /Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 Depositing the precursor solution on a substrate, and carrying out heat treatment on the substrate at the temperature of 400-450 ℃ for 10-12 minutes to obtain the material matrix.
S3: and (2) soaking the material substrate in 0.2-0.3mol/L silver nitrate solution for 1-5 minutes, taking out the material substrate, and then performing heat treatment at 700-850 ℃ for 2-30 minutes to obtain a material intermediate, wherein the content of silver element in the material intermediate is 0.5-5%.
During the soaking process, silver nitrate solution is attached to the surface of the material matrix, and under the high-temperature condition, because silver nitrate cannot enter Li 4 Ti 5 O 12 And Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 And the silver nitrate is decomposed into simple substance silver to be attached to the surface of the material matrix when being heated at high temperature.
S4: and (3) evaporating a 1-3 mu m Mo layer on the surface of the material intermediate body to obtain the thin-film lithium ion battery composite negative electrode material.
Because the evaporation temperature of Mo is higher than the melting temperature of silver, in the evaporation process, the high-temperature gasified Mo particles can re-melt the silver layer on the surface of the material matrix and combine with Mo to form a composite coating, thereby increasing the adhesive force of the composite coating and the material matrix. And the addition of Mo can also increase the strength and toughness of the plating layer and prolong the service life of the cathode.
Due to Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 Is an excellent lithium ion conductor, and the molybdenum-silver coating is an excellent electronic conductor, so that the preparation method is realizedThe composite cathode material of the thin-film lithium ion battery can improve Li simultaneously 4 Ti 5 O 12 Ion and electron conductivity of the film, reduction of Li 4 Ti 5 O 12 A sheet resistance.
The invention also provides a thin film lithium ion battery composite negative electrode material prepared by the preparation method.
Preferably, the thickness of the composite negative electrode material of the thin-film lithium ion battery is less than 100 micrometers.
Example 1
Weighing 1.9765 mol of lithium acetate, 0.0015g of aluminum nitrate and 0.015g of tributyl phosphate, dissolving the lithium acetate, the aluminum nitrate and the tributyl phosphate into 1000 ml of ethanol, fully stirring, and dripping 2.471 mol of isopropyl titanate into the mixed solution under the condition of continuous stirring after all solutes are completely dissolved to obtain Li 4 Ti 5 O 12 /Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 Precursor solution;
spray pyrolysis method is adopted to lead Li 4 Ti 5 O 12 /Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 Deposition of precursor solution on Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 Sintering sheet at 380 deg.c, nozzle and Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 The distance between the solid electrolyte sintered sheets is 8cm, and the deposited film is subjected to heat treatment at 800 ℃ for 10 minutes to obtain a material matrix;
placing the material matrix into 0.2mol/L silver nitrate solution to be soaked for 1 minute, taking out the material matrix, and then placing the material matrix at the temperature of 700 ℃ to be subjected to heat treatment for 2 minutes to obtain a material intermediate, wherein the content of silver element in the material intermediate is 0.5%;
and evaporating a 1-micron Mo layer on the surface of the material intermediate to obtain the film lithium ion battery composite negative electrode material.
The thickness of the thin film lithium ion battery composite negative electrode material is 20 mu m, and Li in the thin film lithium ion battery composite negative electrode material 4 Ti 5 O 12 、Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 The ratio of the amount of Ag material is 0.985.
Example 2
Weighing 1.765 mol of lithium acetate, 0.015 mol of aluminum nitrate and 0.15 mol of ammonium dihydrogen phosphate, dissolving in 1000 ml of ethylene glycol monomethyl ether, then dropwise adding 5 ml of concentrated nitric acid, fully stirring, dropwise adding 2.21 mol of tetrabutyl titanate into the mixed solution under the condition of continuous stirring after all solutes are completely dissolved to obtain Li 4 Ti 5 O 12 /Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 Precursor solution;
li is coated by spin coating 4 Ti 5 O 12 /Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 Deposition of precursor solution on Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 Obtaining a wet film on a sintering sheet, heating the obtained wet film to 350 ℃ in air at a heating rate of 10 ℃/min for 20 minutes, then repeatedly carrying out rotary coating and heating decomposition to obtain a film with required thickness, and finally carrying out heat treatment in an air atmosphere at 800 ℃ for 5 minutes to obtain a material substrate;
placing the material matrix into 0.25mol/L silver nitrate solution to be soaked for 2 minutes, taking out the material matrix, and then placing the material matrix at the temperature of 800 ℃ to be subjected to heat treatment for 20 minutes to obtain a material intermediate, wherein the content of silver element in the material intermediate is 5%;
and (3) evaporating a 2-micron Mo layer on the surface of the material intermediate to obtain the film lithium ion battery composite negative electrode material.
The thickness of the thin film lithium ion battery composite negative electrode material is 30 mu m, and Li in the thin film lithium ion battery composite negative electrode material 4 Ti 5 O 12 、Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 The ratio of the amount of Ag substance is 0.85.
Example 3
1.752 mol of lithium acetate, 0.012 mol of aluminum nitrate and 0.12 mol of ammonium dihydrogen phosphate are weighed and dissolved in 1000 ml of ethanol, then 5 ml of concentrated nitric acid is dripped in, and the mixture is fully stirred until all solutes are completely dissolvedAfter dissolution, 2.318 mol of tetrabutyl titanate is added into the mixed solution dropwise under the condition of continuous stirring to obtain Li 4 Ti 5 O 12 /Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 Precursor solution;
li is coated by spin coating 4 Ti 5 O 12 /Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 Depositing the precursor solution on a silicon wafer to obtain a wet film, heating the wet film to 380 ℃ in air at a heating rate of 10 ℃/min for 20 minutes, then repeatedly performing rotary coating and thermal decomposition to obtain a thin film with required thickness, and finally performing heat treatment at 800 ℃ in an air atmosphere for 5 minutes to obtain a material substrate;
placing the material matrix into 0.3mol/L silver nitrate solution to be soaked for 5 minutes, taking out the material matrix, and then placing the material matrix at 850 ℃ for heat treatment for 30 minutes to obtain a material intermediate, wherein the content of silver element in the material intermediate is 2%;
and (3) evaporating a 1-micrometer Mo layer on the surface of the material intermediate to obtain the film lithium ion battery composite negative electrode material, wherein the content of silver in the film lithium ion battery composite negative electrode material is 2%.
The thickness of the thin film lithium ion battery composite negative electrode material is 8 mu m, and Li in the thin film lithium ion battery composite negative electrode material 4 Ti 5 O 12 、Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 The ratio of the amount of Ag material is 0.9.
Example 4
Weighing 1.8925 mol of lithium acetate, 0.0075 mol of aluminum nitrate and 0.075 mol of tributyl phosphate, dissolving in 1000 ml of ethanol, stirring, and dripping 2.3675 mol of tetrabutyl titanate into the mixed solution under the condition of continuous stirring after all solutes are dissolved to obtain Li 4 Ti 5 O 12 /Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 Precursor solution;
spraying Li 4 Ti 5 O 12 /Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 The precursor solution is deposited on a platinized silicon wafer, the temperature of the platinized silicon wafer is controlled at 400 ℃, and a nozzle and Li are mixed 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 The distance between the solid electrolyte sintering sheets is 8cm, and finally the deposited film is subjected to heat treatment for 5 minutes at 800 ℃ in air atmosphere to obtain a material matrix;
placing the material matrix into a silver nitrate solution to be soaked for 4 minutes, taking out the material matrix, and then placing the material matrix at the temperature of 700 ℃ to be subjected to heat treatment for 18 minutes to obtain a material intermediate, wherein the content of silver element in the material intermediate is 2%;
and (3) evaporating a 3-micrometer Mo layer on the surface of the intermediate material to obtain the thin-film lithium ion battery composite negative electrode material.
The thickness of the thin film lithium ion battery composite negative electrode material is 10 mu m, and Li in the thin film lithium ion battery composite negative electrode material 4 Ti 5 O 12 、Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 The ratio of the amount of Ag substance is 0.93.
Compared with the prior art, the Li can be obtained by adopting soluble lithium salt, aluminum nitrate, titanium organic compound and phosphorus-containing compound as raw materials in proper proportion and controlling the synthesis conditions 4 Ti 5 O 12 /Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 Finally, a Mo/Ag composite coating is plated on the material substrate. Due to Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 Is an excellent lithium ion conductor, the Mo/Ag composite coating is an excellent electronic conductor, and the prepared Li 4 Ti 5 O 12 The thin film contains Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 And the Mo/Ag composite coating can improve Li at the same time 4 Ti 5 O 12 Ion and electron conductivity of the film, reduction of Li 4 Ti 5 O 12 The film resistance is beneficial to preparing the low-resistance film lithium ion battery.

Claims (9)

1. A preparation method of a composite cathode material of a thin-film lithium ion battery is characterized by comprising the following steps:
s1: dissolving lithium salt, aluminum nitrate and phosphorus-containing compound in solvent, and then dripping organic titanium compound to obtain Li 4 Ti 5 O 12 /Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 Precursor solution of the Li 4 Ti 5 O 12 /Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 The ratio of the amount of lithium, aluminum, titanium and phosphorus in the precursor solution is (3.53-3.953): (0.03-0.003): 4.42-4.942): 0.3-0.03;
s2: the Li is subjected to spray pyrolysis or spin coating 4 Ti 5 O 12 /Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 Depositing the precursor solution on a substrate, and performing heat treatment on the substrate at the temperature of 400-450 ℃ for 10-12 minutes to obtain a material matrix;
s3: soaking the material matrix in 0.2-0.3mol/L silver nitrate solution for 1-5 minutes, taking out, and then placing at 700-850 ℃ for heat treatment for 2-30 minutes to obtain a material intermediate, wherein the content of silver element in the material intermediate is 0.5-5%;
s4: and (3) evaporating a 1-3 mu m Mo layer on the surface of the intermediate material to obtain the thin-film lithium ion battery composite negative electrode material.
2. The preparation method of the thin-film lithium ion battery composite anode material according to claim 1, wherein the solvent is ethanol or ethylene glycol monomethyl ether.
3. The method for preparing the thin-film lithium ion battery composite anode material according to claim 1, wherein the lithium salt is lithium acetate or lithium nitrate.
4. The method for preparing the thin-film lithium ion battery composite anode material according to claim 1, wherein the titanium organic compound is titanate.
5. The preparation method of the thin-film lithium ion battery composite anode material according to claim 4, wherein the titanium organic compound is tetrabutyl titanate or isopropyl titanate.
6. The method for preparing the thin-film lithium ion battery composite anode material according to claim 1, wherein the phosphorus-containing compound is ammonium dihydrogen phosphate, trimethyl phosphate, triethyl phosphate, tripropyl phosphate, or tributyl phosphate.
7. The preparation method of the thin-film lithium ion battery composite anode material according to claim 1, wherein the substrate is a silicon wafer, a platinized silicon wafer or a lithium ion solid electrolyte Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 And sintering the sheet.
8. The composite negative electrode material of the thin-film lithium ion battery is characterized by being prepared by the preparation method of any one of claims 1 to 7.
9. The thin-film lithium ion battery composite anode material of claim 8, wherein the thickness of the thin-film lithium ion battery composite anode material is less than 100 μm.
CN202110631096.1A 2021-06-07 2021-06-07 Composite negative electrode material of thin-film lithium ion battery and preparation method thereof Active CN113380971B (en)

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CN101609883B (en) * 2009-07-13 2011-01-05 北京安华联合能源科技有限责任公司 Preparation method of nano-silver particle dispersed Li4Ti5O12 thin film lithium ion battery negative electrode
CN101673846A (en) * 2009-09-28 2010-03-17 吴显明 All solid state lithium ion thin-film battery
CN105789583B (en) * 2016-03-28 2018-08-14 辽宁大学 A kind of lithium ion battery negative material Li4Ti5O12/TiO2/ Ag and preparation method thereof
CN105655563B (en) * 2016-03-30 2018-02-27 吉首大学 A kind of composite cathode material for lithium ion cell and preparation method thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005119816A1 (en) * 2004-05-28 2005-12-15 Commissariat A L'energie Atomique Polymer separator for a lithium battery
JP2010040439A (en) * 2008-08-07 2010-02-18 Sumitomo Electric Ind Ltd Lithium battery
FR2956523A1 (en) * 2010-02-18 2011-08-19 Centre Nat Rech Scient PROCESS FOR PREPARING A MONOLITHIC BATTERY BY PULSE CURRENT SINTING

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