CN107293698A - A kind of preparation method of tin ash/carbon negative pole material - Google Patents
A kind of preparation method of tin ash/carbon negative pole material Download PDFInfo
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- CN107293698A CN107293698A CN201610190416.3A CN201610190416A CN107293698A CN 107293698 A CN107293698 A CN 107293698A CN 201610190416 A CN201610190416 A CN 201610190416A CN 107293698 A CN107293698 A CN 107293698A
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- tin
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- negative pole
- deionized water
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/362—Composites
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/052—Li-accumulators
- H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/58—Selection 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
- H01M4/583—Carbonaceous material, e.g. graphite-intercalation compounds or CFx
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
- H01M4/624—Electric conductive fillers
- H01M4/625—Carbon or graphite
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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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- Inorganic Chemistry (AREA)
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- Manufacturing & Machinery (AREA)
- Battery Electrode And Active Subsutance (AREA)
Abstract
Added the invention discloses a kind of preparation method of tin ash/carbon negative pole material, including by citric acid and glucose in deionized water, stir to clarify, form solution A;In the deionized water that Tin tetrachloride pentahydrate is added to 50 milliliters, stirring forms tin chloride solution B;Under stirring condition, solution A is slowly dropped into tin chloride solution B, continuing stirring makes solution form uniform suspension, is put into baking oven and is heated to 120 DEG C, is incubated 6 hours, obtains sediment;Dry, then calcined under argon gas protection at 60 DEG C after being centrifuged, cleaned to sediment with ethanol and deionized water, that is, obtain tin ash/carbon composite.Preparation technology of the present invention is simple, is not introduced into strong acid and strong base or other noxious materials, employs the route of green syt, and prepared negative material cycle performance is good, and specific capacity is high.
Description
Technical field
The present invention relates to technical field of lithium ion, and in particular to a kind of preparation method of tin ash/carbon negative pole material.
Background technology
Electrode material is the key of lithium ion battery.At present, commercialized lithium ion battery negative material is mainly graphite, graphite cost is low, wide material sources, suitable for commercialization, but can form SEI films after the embedding lithium of graphite, cause the irreversible loss of initial capacity, make its capacity relatively low, theoretical capacity is only 372 mAh/g, the application in the field for needing high-energy output is restricted.And Carbon anode current potential and lithium metal current potential closely, the easy precipitating metal lithium in Carbon anode surface formation Li dendrite causes battery short circuit, there is certain potential safety hazard.Metal oxide such as Fe2O3, SnO2There is very high specific capacity Deng as lithium ion battery negative material.Wherein SnO2Specific capacity is up to 782 mAh/g, but SnO2As electrode material, Volume Changes are up to 200~300% in charge and discharge process, and this can cause the efflorescence of electrode, cause the open circuit of active material and collector.Therefore, most of SnO2All there is the problem of capacity attenuation is rapid in electrode, the development as lithium ion battery negative material and practical application which also limits metal oxide.Therefore, researchers are conducted in-depth research to this, including being coated to material, doping vario-property, it is prepared into compound or nano material etc., the performance of electrode material is improved by these methods, particularly metal oxide carries out the compound of nanoscale with Carbon Materials, prepares new nanostructured and has become the focus studied at present.
The content of the invention
Regarding the issue above, the present invention provides a kind of preparation method of tin ash/carbon negative pole material.
The technical scheme for realizing the object of the invention is:
A kind of preparation method of tin ash/carbon negative pole material, comprises the following steps:
(1)By Tin tetrachloride pentahydrate:Citric acid:Glucose or sucrose are 2:0.5:0.5~1 mass ratio is weighed, and citric acid and glucose are added in 30-50 ml deionized waters, stirred to clarify, solution A is formed;
(2)In the deionized water that Tin tetrachloride pentahydrate is added to 50 milliliters, stirring forms tin chloride solution B;
(3)Under agitation, toward solution A is slowly dropped into tin chloride solution B, continuing stirring makes solution form uniform suspension, is put into baking oven and is heated to 120 DEG C, is incubated 6 hours, obtains sediment;
(4)Sediment is centrifuged with ethanol and deionized water, cleaned, is dried, then is calcined under argon gas protection, that is, obtains tin ash/carbon negative pole material.
The temperature of the calcining is 300 to 500 DEG C, and calcination time is 3 to 5 hours.
Advantages of the present invention is:Preparation technology of the present invention is simple, is not introduced into strong acid and strong base or other noxious materials, employs the route of green syt, and prepared tin ash/carbon negative pole material cycle performance is good, and specific capacity is high.
Embodiment
Embodiment 1
(1)0.5 gram of citric acid and 1 gram of glucose are added in 50 ml deionized waters, stirs to clarify, forms solution A;
(2)In the deionized water that 2 grams of Tin tetrachloride pentahydrates are added to 50 milliliters, stirring forms tin chloride solution B;
(3)Under agitation, toward solution A is slowly dropped into tin chloride solution B, continuing stirring makes solution form uniform suspension, is put into baking oven and is heated to 120 DEG C, is incubated 6 hours, obtains sediment;
(4)Sediment is centrifuged with ethanol and deionized water, cleans after three times and to be dried at 60 DEG C, then 300 DEG C of calcinings obtain tin ash/carbon negative pole material after 5 hours under argon gas protection.
Embodiment 2
(1)0.5 gram of citric acid and 0.5 gram of sucrose are added in 30 ml deionized waters, stirs to clarify, forms solution A;
(2)In the deionized water that 2 grams of Tin tetrachloride pentahydrates are added to 50 milliliters, stirring forms tin chloride solution B;
(3)Under agitation, toward solution A is slowly dropped into tin chloride solution B, continuing stirring makes solution form uniform suspension, is put into baking oven and is heated to 120 DEG C, is incubated 6 hours, obtains sediment;
(4)Sediment is centrifuged with ethanol and deionized water, cleans after three times and is dried at 60 DEG C, then after 500 DEG C under argon gas is protected are calcined 3 hours, that is, obtains tin ash/carbon negative pole material.
Claims (2)
1. a kind of preparation method of tin ash/carbon negative pole material, it is characterised in that comprise the following steps:
(1)By Tin tetrachloride pentahydrate:Citric acid:Glucose or sucrose are 2:0.5:0.5~1 mass ratio is weighed, and citric acid and glucose are added in 30-50 ml deionized waters, stirred to clarify, solution A is formed;
(2)In the deionized water that Tin tetrachloride pentahydrate is added to 50 milliliters, stirring forms tin chloride solution B;
(3)Under agitation, toward solution A is slowly dropped into tin chloride solution B, continuing stirring makes solution form uniform suspension, is put into baking oven and is heated to 120 DEG C, is incubated 6 hours, obtains sediment;
(4)Sediment is centrifuged by ethanol and deionized water, cleaned, is dried, then is calcined under argon gas protection, that is, obtains tin ash/carbon negative pole material.
2. a kind of preparation method of tin ash/carbon negative pole material according to claim 1, it is characterised in that the temperature of the calcining is 300 to 500 DEG C, calcination time is 3 to 5 hours.
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CN201610190416.3A CN107293698A (en) | 2016-03-30 | 2016-03-30 | A kind of preparation method of tin ash/carbon negative pole material |
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CN201610190416.3A CN107293698A (en) | 2016-03-30 | 2016-03-30 | A kind of preparation method of tin ash/carbon negative pole material |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108258216A (en) * | 2018-01-11 | 2018-07-06 | 电子科技大学 | Biomass carbon-tin energy storage material and preparation method thereof |
CN108400315A (en) * | 2018-01-29 | 2018-08-14 | 北京航空航天大学 | A kind of preparation method of the ion battery cathode material of carbon-coated antimony doping stannic oxide |
CN112436127A (en) * | 2020-12-02 | 2021-03-02 | 天津工业大学 | Preparation method of novel nano-structure tin-carbon composite negative electrode material |
CN113880130A (en) * | 2021-12-06 | 2022-01-04 | 中博龙辉装备集团股份有限公司 | Stannous sulfide carbon composite material and preparation method and application thereof |
-
2016
- 2016-03-30 CN CN201610190416.3A patent/CN107293698A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108258216A (en) * | 2018-01-11 | 2018-07-06 | 电子科技大学 | Biomass carbon-tin energy storage material and preparation method thereof |
CN108400315A (en) * | 2018-01-29 | 2018-08-14 | 北京航空航天大学 | A kind of preparation method of the ion battery cathode material of carbon-coated antimony doping stannic oxide |
CN112436127A (en) * | 2020-12-02 | 2021-03-02 | 天津工业大学 | Preparation method of novel nano-structure tin-carbon composite negative electrode material |
CN113880130A (en) * | 2021-12-06 | 2022-01-04 | 中博龙辉装备集团股份有限公司 | Stannous sulfide carbon composite material and preparation method and application thereof |
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