CN101106189A - Making method for nano LiFePO4-carbon composite cathode material - Google Patents
Making method for nano LiFePO4-carbon composite cathode material Download PDFInfo
- Publication number
- CN101106189A CN101106189A CNA2006101481216A CN200610148121A CN101106189A CN 101106189 A CN101106189 A CN 101106189A CN A2006101481216 A CNA2006101481216 A CN A2006101481216A CN 200610148121 A CN200610148121 A CN 200610148121A CN 101106189 A CN101106189 A CN 101106189A
- Authority
- CN
- China
- Prior art keywords
- carbon
- preparation
- nano
- composite cathode
- lifepo
- 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.)
- Granted
Links
Images
Classifications
-
- 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
Landscapes
- Battery Electrode And Active Subsutance (AREA)
Abstract
The invention relates to a method for preparing a nano-ferrous lithium phosphate-carbon compound positive material, which is characterized in that based on the ethers organic solvent system and by a sol-process of precursor materials, the mixture at the molecular level of Fe3+, Li+1 and PO42- is realized, and then the technology of low-temperature sintering is used to prepare. Ferrous lithium phosphate in the prepared compound material is in an olivine type with carbon wrapping outside in an amorphous form and the particle size of 45-60nm, and a stable charging and discharging voltage platform at 3.4V is provided, and the charging-discharging capacity under the current of 2C can reach to 133mAh/g. The invention is characterized by simple technique, environment-friendly performance and so on.
Description
Technical field
The present invention relates to a kind of preparation method of anode composite material of lithium ion battery, particularly a kind of preparation method of nano LiFePO 4-carbon composite cathode material.Belong to the lithium ion battery material field.
Background technology
What at present, the research of anode material for lithium-ion batteries mainly concentrated on Co, Ni and Mn contains potassium transition metal oxide aspect.LiCoO
2Be the positive electrode of unique large-scale commercial, the research comparative maturity, high comprehensive performance, but the preparation cost height of material, and also thermal stability is relatively poor, and toxicity is bigger, has certain safety issue, and the new material that needs to seek high-performance and low-cost replaces it.LiNiO
2Have higher specific discharge capacity and lower preparation cost, but its preparation condition harshness, and its crystal structure decay of generation from three parts to the monocline easily in charge and discharge process, capacitance descends very fast, material poor heat stability in addition,＞200 ℃ are just easily decomposed and produce O
2, have comparatively serious safety problem.Spinel-type LiMn
2O
4Cost is low, and fail safe is good, but cycle performance especially high temperature cyclic performance is poor, certain dissolubility is arranged in electrolyte, storge quality is poor.The research of two yuan or multi-element composite positive pole material mainly concentrates on LiNi
1-xCo
xO
2And LiNi
xCo
yMn
1-x-yO
2The lamellar compound aspect, they are than LiCoO
2Positive electrode has advantages such as the cost of raw material is lower, specific capacity is higher, energy density is bigger, and fail safe is better, but large current discharging capability and tap density are than LiCoO
2On the low side, preparation cost increases, and has increased the difficulty of carrying out the secondary resource recovery from now on to a certain extent.Therefore, the novel anode material of further researching and developing high energy, safety, environmental protection becomes the research focus of lithium ion battery circle.
LiFePO 4 (LiFePO
4) material has abundant raw material, cost is low, specific capacity is higher, thermal stability and cyclical stability is good, nontoxic, environmental friendliness etc. is outstanding advantages, from people such as Padhi in 1997 first with the LiFePO of quadrature olivine structural
4As anode material for lithium-ion batteries, the research of this material is become gradually the research focus of various countries' researcher.It is the lithium ion cell positive substitution material of future generation that has much potentiality.But the conductivity of this material is very poor, can only discharge and recharge under minimum multiplying power under the room temperature, has influenced its high rate performance; In addition, preparation technology is usually with Fe
2+As source of iron, price is than Fe
3+Salt is high and need multistep to grind and heat treatment step, and preparation technology is complicated, and product purity is not easy control, thereby cost is increased, and these have all hindered its application in practical lithium-ion.
Summary of the invention
The preparation method who the purpose of this invention is to provide a kind of original position carbon-coated nano LiFePO 4 is by the synthetic Li that shortens of nano material as far as possible
+Diffusion length, increasing specific surface area in conjunction with original position carbon-coated nano particle, improves the apparent lithium ion conductivity and the diffusion coefficient of material greatly, thereby prepares the good nanometer LiFePO of chemical property
4/ C composite material.Promptly based on the ether organic solvent system, by the process realization Fe of simple sol-gelization
3+, Li
+And PO
4 2-Molecular level mix, obtain the nano LiFePO 4-carbon composite material by low-temperature sintering then.
1. the preparation method of nano LiFePO 4-carbon composite cathode material comprises as follows:
1) with Fe
3+Compound is dissolved in the ether organic solvent, at room temperature fully mix stirring, be mixed with 1～2mol/L solution, according to Li: Fe: the P mol ratio is to take by weighing lithium salts and phosphate at 1: 1: 1, mix excessive carbon source (consumption of carbon source makes that carbon content is 1～10% in the product), add distilled water and make it dissolving, then with contain the homodisperse colloidal sol of the miscible formation of ethereal solution, and the stirring evaporation became gel in 3～8 hours under 60～80 ℃, last vacuumize obtains lithium iron phosphate precursor to xerogel;
2) lithium iron phosphate precursor being put into tube type resistance furnace, is under 5～50 liters/minute the inert gas protection, in 250 ℃～500 ℃ preliminary treatment 0.5～5 hour, to get rid of residual moisture and CO in the presoma at flow velocity
2, NH
3Deng gas;
3) mixture that preliminary treatment obtained grinds evenly, and under identical inert atmosphere, heat treatment is 4～24 hours under 550 ℃～800 ℃ temperature, is cooled to room temperature and promptly obtains the nano-lithium iron phosphate composite material that carbon coats (average grain particle diameter＜100nm).
Organic solvent used in the present invention is gylcol ether, diethylene glycol (DEG) ethers, propylene glycol ethers etc.
The used molysite of the present invention can be selected from ferric nitrate, ironic citrate, ferric acetate etc.; Lithium salts can be selected from lithium hydroxide, lithium acetate etc., and phosphate can be phosphoric acid, perhaps adopts lithium salts and phosphatic combination LiH
2PO
4
The carbon source that the present invention uses is sucrose, glucose, maltose, fructose or lactose etc.It mainly plays reducing agent (reduction Fe
3+Be Fe
2+) and increase the promotion of solution phase viscosity, the sol-gel conversion process plays the effect of carbon original position clad nano LiFePO 4 simultaneously.
The gas that the present invention uses is the mist (volume content of hydrogen is 2～10% in the mist) of argon gas, nitrogen, argon gas and hydrogen.
The present invention is based on the ether organic solvent system, the sol-gel process by precursor material has prepared the nano LiFePO 4-carbon composite material in conjunction with the low-temperature bake Technology for Heating Processing.LiFePO 4 is an olivine-type in the prepared composite material, and carbon is coated on outside it with amorphous form, and average grain diameter is between 45-60nm.This anode composite material has the charging/discharging voltage platform about 3.4V stably, and electric conductivity and heavy-current discharge performance are good, and charging and discharging capacity reversible under the 2C electric current reaches 133mAh/g; This composite structure is stable, and cyclical stability is good; This composite material does not contain Co, Ni etc. has the element of bigger pollution to environment, thereby is environmentally friendly material; The raw material that is adopted is Fe
3+Compound, cheap, wide material sources, and process route is simple, the cycle is shorter, energy consumption is low, is fit to the scale volume production.
Description of drawings
Fig. 1 is the X ray diffracting spectrum by the prepared nano LiFePO 4-carbon composite cathode material of embodiment 1, adopts Rigaku-D/MAX 2200 type X ray polycrystalline diffractometer (Cu target k
αRay, wavelength X=0.1540562nm).
Fig. 2 is FE-SEM (the Field emission scan electron microscope) photo according to the prepared nano LiFePO 4-carbon composite cathode material of embodiment 1, adopts S-4700 type field emission scanning electron microscope, and multiplication factor is 80000 times.
Fig. 3 is that voltage range is 2.5-4.2V according to the prepared discharge curve of simulation lithium ion battery under different charge-discharge magnifications of embodiment 1, and electrolyte is 1mol/L LiPF
6/ EC-DMC (1: 1), charge-discharge magnification is respectively 0.2C, 0.5C, 2C, and the measurement temperature is a room temperature.
Fig. 4 is that voltage range is 2.5-4.2V according to the prepared cycle performance curve of simulation lithium ion battery under different charge-discharge magnifications of embodiment 1, and electrolyte is 1mol/L LiPF
6/ EC-DMC (1: 1), charge-discharge magnification is respectively 0.2C, 0.5C, 2C, and the measurement temperature is a room temperature.
Embodiment
Embodiment 1
1) takes by weighing 0.5molFe (NO
3)
39H
2O is dissolved in the EGME organic solvent, at room temperature fully mix stirring, be mixed with 1.5mol/L solution, take by weighing 0.5mol lithium dihydrogen phosphate and excessive sucrose (consumption of sucrose makes that carbon content is 6% in the product), add distilled water 50ml, make it dissolving, mix with EGME solution then and form homodisperse colloidal sol, and under 70 ℃, stir 6 hours one-tenth of evaporation gel, last vacuumize obtains lithium iron phosphate precursor to xerogel;
2) lithium iron phosphate precursor being put into tube type resistance furnace, is under 5～50 liters/minute the argon stream protection, in 300 ℃ of preliminary treatment 5 hours at flow velocity;
3) mixture that preliminary treatment is obtained grinds evenly, and under the argon gas atmosphere, heat treatment is 10 hours under 725 ℃ of temperature, is cooled to room temperature and promptly obtains the nano-lithium iron phosphate composite material that carbon coats.
What record the content of residual carbon in the gained composite material and actual design quite is about 6.12%, and its XRD spectra is seen Fig. 1, and the reference standard card is the intact olivine-type LiFePO of crystalline form
4(belong to Pnma space group), and fail to observe the diffraction maximum of carbon, illustrate that residual carbon mainly exists with the form of amorphous carbon.Fig. 2 is the FE-SEM surface topography analysis chart under 80000 times of the multiplication factors, and the gained material is average grain diameter equally distributed nano particle between 45 to 60nm as we can see from the figure, and does not significantly reunite.
Composite material with embodiment 1 gained is made electrode according to following method.
Take by weighing the composite material of embodiment 1 gained respectively with 80: 10: 10 mass ratioes: conductive carbon (SuperP): polytetrafluoroethylene (PTFE) grinds mixing and paint electrode on aluminium foil, 120 ℃ of vacuum obtained positive plate in dry 24 hours, with the pure metal lithium sheet is negative pole, to be dissolved in the 1.0mol/L LiPF in ethylene fat+dimethyl carbonate (volume ratio is 1: 1) mixed solvent
6Be electrolyte, the polypropylene microporous membrane is a diaphragm material, forms the simulation lithium ion battery.From Fig. 3, can see on the discharge curve of 0.2C multiplying power when the 2.5V-4.2V cut-ff voltage, the battery of surveying has 3.42V discharge voltage plateau stably, the reversible specific capacity that can calculate composite material among this embodiment is 152mAh/g, and reversible specific capacity can reach 133mAh/g under the 2C multiplying power.Fig. 4 is the respective battery cycle performance under 0.2C, 0.5C and 2C multiplying power respectively.Wherein, specific capacity is with LiFePO
4Mass Calculation, but not LiFePO
4The quality of+carbon composite.
1) takes by weighing 0.5molFe (NO
3)
39H
2O is dissolved in the propylene glycol monomethyl ether organic solvent, at room temperature fully mix stirring, be mixed with 1.5mol/L solution, take by weighing 0.5mol potassium dihydrogen phosphate and excessive sucrose (consumption of sucrose makes that carbon content is 6% in the product), add distilled water 50ml, make it dissolving, form homodisperse colloidal sol with the propylene glycol monomethyl ether solution blending then, and under 70 ℃, stir 6 hours one-tenth of evaporation gel, last vacuumize obtains lithium iron phosphate precursor to xerogel;
2) lithium iron phosphate precursor being put into tube type resistance furnace, is under 5～50 liters/minute the argon stream protection, in 300 ℃ of preliminary treatment 5 hours at flow velocity;
3) mixture that preliminary treatment is obtained grinds evenly, and under the argon gas atmosphere, heat treatment is 10 hours under 725 ℃ of temperature, is cooled to room temperature and promptly obtains the nano-lithium iron phosphate composite material that carbon coats.All the other are with embodiment 1.
Embodiment 3
1) taking by weighing the 0.5mol ironic citrate is dissolved in the EGME organic solvent, at room temperature fully mix stirring, be mixed with 1.5mol/L solution, take by weighing 0.5mol lithium dihydrogen phosphate and excessive sucrose (consumption of sucrose makes that carbon content is 6% in the product), add distilled water 50ml, make it dissolving, mix with EGME solution then and form homodisperse colloidal sol, and under 60 ℃, stir 6 hours one-tenth of evaporation gel, last vacuumize obtains lithium iron phosphate precursor to xerogel;
2) lithium iron phosphate precursor being put into tube type resistance furnace, is under 5～50 liters/minute the argon stream protection, in 300 ℃ of preliminary treatment 5 hours at flow velocity;
3) mixture that preliminary treatment is obtained grinds evenly, and under the argon gas atmosphere, heat treatment is 10 hours under 725 ℃ of temperature, is cooled to room temperature and promptly obtains the nano-lithium iron phosphate composite material that carbon coats.All the other are with embodiment 1.
Embodiment 4
1) takes by weighing 0.5molFe (NO
3)
39H
2O is dissolved in the EGME organic solvent, at room temperature fully mixes stirring, is mixed with 1.5mol/L solution, takes by weighing 0.5mol phosphoric acid and 0.5LiOHH
2O is dissolved in the 200ml distilled water, fully the reaction back adds excessive sucrose (consumption of sucrose makes that residual carbon content is 1～10% in the product), make it dissolving, mix with EGME solution then and form homodisperse colloidal sol, and the stirring evaporation became gel in 6 hours under 70 ℃, last vacuumize obtains lithium iron phosphate precursor to xerogel;
2) lithium iron phosphate precursor being put into tube type resistance furnace, is under 5～50 liters/minute the inert gas protection, in 300 ℃ of preliminary treatment 5 hours at flow velocity;
3) mixture that preliminary treatment is obtained grinds evenly, and under the same inert atmosphere, heat treatment is 10 hours under 725 ℃ of temperature, is cooled to room temperature and promptly obtains the nanometer ferrousphosphate potassium composite material that carbon coats.All the other are with embodiment 1.
Embodiment 5
1) takes by weighing 0.5molFe (NO
3)
39H
2O is dissolved in the EGME organic solvent, at room temperature fully mixes stirring, is mixed with 1.5mol/L solution, takes by weighing 0.5mol phosphoric acid and 0.5LiOHH
2O is dissolved in the 200ml distilled water, fully the reaction back adds excessive glucose (consumption of glucose makes that residual carbon content is 1～10% in the product), make it dissolving, mix with EGME solution then and form homodisperse colloidal sol, and the stirring evaporation became gel in 6 hours under 70 ℃, last vacuumize obtains lithium iron phosphate precursor to xerogel;
2) lithium iron phosphate precursor being put into tube type resistance furnace, is under 5～50 liters/minute the inert gas protection, in 350 ℃ of preliminary treatment 5 hours at flow velocity;
3) mixture that preliminary treatment is obtained grinds evenly, and under the same inert atmosphere, heat treatment is 10 hours under 725 ℃ of temperature, is cooled to room temperature and promptly obtains the nano-lithium iron phosphate composite material that carbon coats.All the other are with embodiment 1.
Claims (8)
1. the preparation method of a nano LiFePO 4-carbon composite cathode material is characterized in that based on the ether organic solvent system, by the colloidal sol process of precursor material, realizes Fe
3+, Li
+ 1And PO
4 2-Molecular level mix, then by the low temperature sintering technology preparation, concrete steps are:
(1) takes by weighing Fe
3+Compound is dissolved in the ether organic solvent, at room temperature fully mix stirring, be mixed with the solution of 1～2mol/L, according to Li: Fe: the P mol ratio is to take by weighing lithium salts and phosphate at 1: 1: 1, mix excessive carbon source, the consumption of carbon source makes that the quality percentage composition of carbon is 1～10% in the end product, add distilled water, make it dissolving, then with contain ethereal solution and dissolve each other and form homodisperse colloidal sol, and stirring flashes to gel under 60～80 ℃, and last vacuumize obtains lithium iron phosphate precursor to xerogel;
(2) lithium iron phosphate precursor being put into tube type resistance furnace, is under 5～50 liters/minute the inert gas protection, in 250 ℃～500 ℃ preliminary treatment at flow velocity;
(3) mixture that preliminary treatment is obtained grinds evenly, under identical inert atmosphere, in 550 ℃～800 ℃ following heat treatments, is cooled to room temperature and promptly obtains the nano-lithium iron phosphate composite material that carbon coats;
Wherein, 1. employed ether organic solvent is gylcol ether, diethylene glycol (DEG) ethers or propylene glycol ethers;
2. described Fe
3+Compound is selected from ferric nitrate, ironic citrate or ferric acetate;
3. described lithium salts is lithium hydroxide or lithium acetate, and phosphate is phosphoric acid or lithium dihydrogen phosphate;
4. described carbon source is sucrose, glucose, maltose, fructose or lactose.
2. the preparation method of nano LiFePO 4-carbon composite cathode material according to claim 1 is characterized in that the time that the 1. middle stirring of step flashes to gel is 3-8 hour.
3. the preparation method of nano LiFePO 4-carbon composite cathode material according to claim 1 is characterized in that the 2. middle pretreatment time of step is 0.5-5 hour.
4. the preparation method of nano LiFePO 4-carbon composite cathode material according to claim 1 is characterized in that the 3. middle heat treatment time of step is 4-24 hour.
5. according to the preparation method of claim 1,3 or 4 described nano LiFePO 4-carbon composite cathode materials, it is characterized in that employed inert gas is the mist of argon gas, nitrogen or argon gas and hydrogen.
6. the preparation method of nano LiFePO 4-carbon composite cathode material according to claim 5, it is characterized in that hydrogen in the mist volume percent content be 2-10%.
7. according to the preparation method of claim 1,2,3,4 or 6 any described nano LiFePO 4-carbon composite cathode materials, it is characterized in that LiFePO 4 is an olivine-type in the prepared composite material, carbon is coated on outside it with amorphous form, and average grain diameter is between 45-60nm.
8. the preparation method of nano LiFePO 4-carbon composite cathode material according to claim 7 is characterized in that described anode composite material has 3.4V charging/discharging voltage platform stably, and charging and discharging capacity reversible under the 2C electric comb reaches 133mAh/g.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006101481216A CN100461507C (en) | 2006-12-27 | 2006-12-27 | Making method for nano LiFePO4-carbon composite cathode material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006101481216A CN100461507C (en) | 2006-12-27 | 2006-12-27 | Making method for nano LiFePO4-carbon composite cathode material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101106189A true CN101106189A (en) | 2008-01-16 |
| CN100461507C CN100461507C (en) | 2009-02-11 |
Family
ID=38999963
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2006101481216A Expired - Fee Related CN100461507C (en) | 2006-12-27 | 2006-12-27 | Making method for nano LiFePO4-carbon composite cathode material |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100461507C (en) |
Cited By (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7722848B2 (en) | 2007-09-25 | 2010-05-25 | Byd Company Limited | Lithium iron phosphate cathode material |
| CN101841016A (en) * | 2010-06-11 | 2010-09-22 | 成都中科来方能源科技有限公司 | Ferrous silicate lithium/carbon/carbon nano tube compound anode material and manufacture method thereof |
| CN101841025A (en) * | 2009-03-16 | 2010-09-22 | Tdk株式会社 | The manufacture method of active material, active material, the lithium rechargeable battery that uses the electrode of this active material and possess this electrode |
| CN101630742B (en) * | 2008-07-15 | 2011-04-13 | 中国科学院化学研究所 | Lithium iron phosphate/carbon nanometer compound and preparation method and application thereof |
| CN102064313A (en) * | 2009-03-12 | 2011-05-18 | 巴莱诺斯清洁能源控股公司 | Open porous electrically conductive nanocomposite material |
| CN102097616A (en) * | 2011-01-11 | 2011-06-15 | 清华大学深圳研究生院 | Preparation method of high-energy and high-power density nano-scale lithium iron phosphate powder |
| US8052897B2 (en) | 2008-02-29 | 2011-11-08 | Byd Company Limited | Composite compound with mixed crystalline structure |
| US8057711B2 (en) | 2008-02-29 | 2011-11-15 | Byd Company Limited | Composite compound with mixed crystalline structure |
| US8062560B2 (en) | 2008-02-29 | 2011-11-22 | Byd Company Limited | Composite compound with mixed crystalline structure |
| US8062559B2 (en) | 2008-02-29 | 2011-11-22 | Byd Company Limited | Composite compound with mixed crystalline structure |
| CN102290565A (en) * | 2011-07-05 | 2011-12-21 | 中国科学院金属研究所 | Preparation method for porous conductive block anode of lithium ion battery |
| US8088305B2 (en) * | 2008-02-22 | 2012-01-03 | Byd Company Limited | Lithium iron phosphate cathode material |
| US8148015B2 (en) | 2008-03-21 | 2012-04-03 | Byd Company Limited | Cathode materials for lithium batteries |
| US8153032B2 (en) | 2008-06-06 | 2012-04-10 | Byd Company Limited | Transition metal hydroxide and oxide, method of producing the same, and cathode material containting the same |
| US8216725B2 (en) | 2008-01-25 | 2012-07-10 | Byd Company Limited | Electrolyte for batteries and battery packs |
| CN103956462A (en) * | 2014-04-28 | 2014-07-30 | 张家港智电芳华蓄电研究所有限公司 | Preparation method of lithium iron phosphate-ferrous lithium carbonate composite electrode material |
| US8883356B2 (en) | 2008-07-30 | 2014-11-11 | Byd Company Limited | Electrolyte for lithium batteries |
| CN104282904A (en) * | 2013-07-03 | 2015-01-14 | 河南科隆新能源有限公司 | Method for improving processing performance and cycle performance of lithium iron phosphate positive electrode material |
| US20150037665A1 (en) * | 2013-01-10 | 2015-02-05 | Lg Chem, Ltd. | Method for preparing lithium iron phosphate nanopowder coated with carbon |
| CN104583130A (en) * | 2013-01-10 | 2015-04-29 | 株式会社Lg化学 | Method for preparing lithium iron phosphate nanopowder |
| CN104603060A (en) * | 2013-01-10 | 2015-05-06 | 株式会社Lg化学 | Method for producing lithium iron phosphate nano powder |
| CN103500832B (en) * | 2013-10-23 | 2017-05-24 | 山东大学 | Method of preparing nanoscale lithium iron phosphate / carbon composite anode material |
| US10076344B2 (en) | 2014-11-19 | 2018-09-18 | Zimmer, Inc. | Gap referencing femoral sizer |
| US11491016B2 (en) | 2013-09-18 | 2022-11-08 | Stryker Corporation | Patient specific bone preparation for consistent effective fixation feature engagement |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4187524B2 (en) * | 2002-01-31 | 2008-11-26 | 日本化学工業株式会社 | Lithium iron phosphorus composite oxide carbon composite, method for producing the same, lithium secondary battery positive electrode active material, and lithium secondary battery |
| CN1280185C (en) * | 2004-02-20 | 2006-10-18 | 北大先行科技产业有限公司 | Preparation process of lithium ferrous phosphate for positive pole of lithium ion cell |
| CN100356617C (en) * | 2005-07-15 | 2007-12-19 | 中国科学院上海微系统与信息技术研究所 | Nanometer phosphate ferrolithium/carbon composite materials, production of solid-phase and use thereof |
-
2006
- 2006-12-27 CN CNB2006101481216A patent/CN100461507C/en not_active Expired - Fee Related
Cited By (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7722848B2 (en) | 2007-09-25 | 2010-05-25 | Byd Company Limited | Lithium iron phosphate cathode material |
| US8216725B2 (en) | 2008-01-25 | 2012-07-10 | Byd Company Limited | Electrolyte for batteries and battery packs |
| US8088305B2 (en) * | 2008-02-22 | 2012-01-03 | Byd Company Limited | Lithium iron phosphate cathode material |
| US8057711B2 (en) | 2008-02-29 | 2011-11-15 | Byd Company Limited | Composite compound with mixed crystalline structure |
| US8062559B2 (en) | 2008-02-29 | 2011-11-22 | Byd Company Limited | Composite compound with mixed crystalline structure |
| US8062560B2 (en) | 2008-02-29 | 2011-11-22 | Byd Company Limited | Composite compound with mixed crystalline structure |
| US8052897B2 (en) | 2008-02-29 | 2011-11-08 | Byd Company Limited | Composite compound with mixed crystalline structure |
| US8148015B2 (en) | 2008-03-21 | 2012-04-03 | Byd Company Limited | Cathode materials for lithium batteries |
| US8153032B2 (en) | 2008-06-06 | 2012-04-10 | Byd Company Limited | Transition metal hydroxide and oxide, method of producing the same, and cathode material containting the same |
| CN101630742B (en) * | 2008-07-15 | 2011-04-13 | 中国科学院化学研究所 | Lithium iron phosphate/carbon nanometer compound and preparation method and application thereof |
| US8883356B2 (en) | 2008-07-30 | 2014-11-11 | Byd Company Limited | Electrolyte for lithium batteries |
| CN102064313B (en) * | 2009-03-12 | 2015-09-02 | 巴莱诺斯清洁能源控股公司 | Open type stephanoporate conductive nano composite material |
| CN102064313A (en) * | 2009-03-12 | 2011-05-18 | 巴莱诺斯清洁能源控股公司 | Open porous electrically conductive nanocomposite material |
| CN101841025A (en) * | 2009-03-16 | 2010-09-22 | Tdk株式会社 | The manufacture method of active material, active material, the lithium rechargeable battery that uses the electrode of this active material and possess this electrode |
| US8524396B2 (en) | 2009-03-16 | 2013-09-03 | Tdk Corporation | Method of manufacturing active material, active material, electrode using the same, and lithium-ion secondary battery equipped therewith |
| CN101841025B (en) * | 2009-03-16 | 2016-04-13 | Tdk株式会社 | Manufacture method, the active material of active material, use the electrode of this active material and possess the lithium rechargeable battery of this electrode |
| CN101841016A (en) * | 2010-06-11 | 2010-09-22 | 成都中科来方能源科技有限公司 | Ferrous silicate lithium/carbon/carbon nano tube compound anode material and manufacture method thereof |
| CN102097616A (en) * | 2011-01-11 | 2011-06-15 | 清华大学深圳研究生院 | Preparation method of high-energy and high-power density nano-scale lithium iron phosphate powder |
| CN102290565A (en) * | 2011-07-05 | 2011-12-21 | 中国科学院金属研究所 | Preparation method for porous conductive block anode of lithium ion battery |
| US10581076B2 (en) | 2013-01-10 | 2020-03-03 | Lg Chem, Ltd. | Method for preparing lithium iron phosphate nanopowder |
| CN104583130A (en) * | 2013-01-10 | 2015-04-29 | 株式会社Lg化学 | Method for preparing lithium iron phosphate nanopowder |
| CN104603060A (en) * | 2013-01-10 | 2015-05-06 | 株式会社Lg化学 | Method for producing lithium iron phosphate nano powder |
| US20150037665A1 (en) * | 2013-01-10 | 2015-02-05 | Lg Chem, Ltd. | Method for preparing lithium iron phosphate nanopowder coated with carbon |
| US10020499B2 (en) * | 2013-01-10 | 2018-07-10 | Lg Chem, Ltd. | Method for preparing lithium iron phosphate nanopowder coated with carbon |
| US9865875B2 (en) | 2013-01-10 | 2018-01-09 | Lg Chem, Ltd. | Method for preparing lithium iron phosphate nanopowder |
| CN104603060B (en) * | 2013-01-10 | 2018-01-26 | 株式会社Lg 化学 | The preparation method of lithium iron phosphate nano powder |
| CN104583130B (en) * | 2013-01-10 | 2017-11-24 | 株式会社Lg 化学 | The preparation method of lithium iron phosphate nano powder |
| CN104282904B (en) * | 2013-07-03 | 2016-12-28 | 河南科隆新能源有限公司 | A kind of method improving lithium iron phosphate positive material processing characteristics and cycle performance |
| CN104282904A (en) * | 2013-07-03 | 2015-01-14 | 河南科隆新能源有限公司 | Method for improving processing performance and cycle performance of lithium iron phosphate positive electrode material |
| US11491016B2 (en) | 2013-09-18 | 2022-11-08 | Stryker Corporation | Patient specific bone preparation for consistent effective fixation feature engagement |
| CN103500832B (en) * | 2013-10-23 | 2017-05-24 | 山东大学 | Method of preparing nanoscale lithium iron phosphate / carbon composite anode material |
| CN103956462A (en) * | 2014-04-28 | 2014-07-30 | 张家港智电芳华蓄电研究所有限公司 | Preparation method of lithium iron phosphate-ferrous lithium carbonate composite electrode material |
| US10076344B2 (en) | 2014-11-19 | 2018-09-18 | Zimmer, Inc. | Gap referencing femoral sizer |
Also Published As
| Publication number | Publication date |
|---|---|
| CN100461507C (en) | 2009-02-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN100461507C (en) | Making method for nano LiFePO4-carbon composite cathode material | |
| CN103515594B (en) | Lithium manganese phosphate/LiFePO4 Core-shell structure material that carbon is coated and preparation method thereof | |
| CN101081696B (en) | Ferric phosphate lithium material for lithium ion powder cell and preparation method thereof | |
| CN102655231B (en) | A kind of method preparing high power performance anode material for lithium-ion batteries LiMn2O4 | |
| CN101591012B (en) | Preparation method of lithium iron phosphate as cathode material of lithium ion battery | |
| CN103219493B (en) | A kind of sulphur conductive oxide composite material and the application as lithium sulfur battery anode material thereof | |
| CN102956887A (en) | Preparation method of nano-grade lithium manganese phosphate anode material | |
| KR20230142698A (en) | Manufacturing method of lithium manganese iron phosphate, cathode material and lithium ion battery | |
| CN109167035A (en) | Carbon-coated ferrous sulfide negative electrode material, preparation method and its sodium-ion battery of preparation | |
| CN101931073B (en) | Preparation method of lithium iron phosphate/carbon composite cathode material | |
| CN105355908A (en) | Composite negative electrode material for lithium ion battery, preparing method thereof, negative electrode using material and lithium ion battery | |
| CN103159264A (en) | Method for preparing positive material NCA of lithium ion cell by virtue of pure solid phase method | |
| CN105226273A (en) | A kind of iron manganese phosphate for lithium and preparation method thereof and application | |
| CN103928680A (en) | Spray drying auxiliary synthesis method for preparing sheet type lithium manganese phosphate/graphene composite material | |
| CN105226267A (en) | Three dimensional carbon nanotubes modifies spinel nickel lithium manganate material and its preparation method and application | |
| CN104868110A (en) | Graphene-oriented mesoporous Co2V2O7 nanosheet material and production method and application thereof | |
| CN104617293A (en) | Preparation method of fluorine-modified carbon-cladded lithium iron phosphate composite material | |
| CN116169264A (en) | Carbon-coated sodium-rich ferric sodium pyrophosphate composite positive electrode material, preparation method and application | |
| Li et al. | Influence of synthesis method on the performance of the LiFePO4/C cathode material | |
| CN102386408B (en) | Preparation method for manganese lithium borate cathode material of lithium ion battery | |
| CN102157727B (en) | Preparation method for nano MnO of negative electrode material of lithium ion battery | |
| CN101593831A (en) | Process for preparing sol-gel based on the lithium iron phosphate cathode material of ferric phosphate | |
| CN100527482C (en) | Making method for LiFePO4-carbon composite cathode material of lithium ion battery | |
| CN114171729A (en) | Preparation method of graphene-based lithium iron phosphate positive electrode material | |
| CN102079517A (en) | Method for preparing fluorizated lithium vanadium phosphate as lithium-ion battery anode material by using spray pyrolysis method |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C17 | Cessation of patent right | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20090211 Termination date: 20100127 |