CN104393293A - Positive pole lithium iron phosphate/carbon composite material for low-temperature battery and preparation method of composite material - Google Patents
Positive pole lithium iron phosphate/carbon composite material for low-temperature battery and preparation method of composite material Download PDFInfo
- Publication number
- CN104393293A CN104393293A CN201410667397.XA CN201410667397A CN104393293A CN 104393293 A CN104393293 A CN 104393293A CN 201410667397 A CN201410667397 A CN 201410667397A CN 104393293 A CN104393293 A CN 104393293A
- Authority
- CN
- China
- Prior art keywords
- lithium
- iron phosphate
- lithium iron
- compound
- low
- 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
Links
Classifications
-
- 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
- H01M4/587—Carbonaceous material, e.g. graphite-intercalation compounds or CFx for inserting or intercalating light metals
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B25/00—Phosphorus; Compounds thereof
- C01B25/16—Oxyacids of phosphorus; Salts thereof
- C01B25/26—Phosphates
- C01B25/45—Phosphates containing plural metal, or metal and ammonium
-
- 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
- H01M4/5825—Oxygenated metallic salts or polyanionic structures, e.g. borates, phosphates, silicates, olivines
-
- 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
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Battery Electrode And Active Subsutance (AREA)
Abstract
本发明公开了一种低温电池用正极材料磷酸铁锂/碳复合材料的制备方法。该方法是采用二价铁化合物为原料，按照摩尔比为Fe：Li：P＝0.98-1:1-1.02:1的比例称取二价铁化合物、锂化合物和磷化合物，各自溶解或分散在去离子水中，以一定顺序加入到适量体积的液相还原剂中，在特定温度下回流反应，固液分离后得到磷酸铁锂前驱体，再惰性气体保护下煅烧制得LiFePO4/C复合正极材料。与其他方法相比，本发明工艺设备简单，条件温和，前驱体结晶完整，高温煅烧时间大大缩短，能耗大幅度降低，磷酸铁锂粒径细小，具有较优异的常温放电性能和低温充放电性能。
The invention discloses a method for preparing a positive electrode material lithium iron phosphate/carbon composite material for a low-temperature battery. The method is to use a ferrous compound as a raw material, weigh the ferrous compound, lithium compound and phosphorus compound according to the molar ratio of Fe:Li:P=0.98-1:1-1.02:1, dissolve or disperse them in Add deionized water to an appropriate volume of liquid-phase reducing agent in a certain order, reflux reaction at a specific temperature, and obtain a lithium iron phosphate precursor after solid-liquid separation, and then calcinate under the protection of an inert gas to obtain a LiFePO 4 /C composite positive electrode Material. Compared with other methods, the present invention has simple process equipment, mild conditions, complete precursor crystallization, greatly shortened high-temperature calcination time, greatly reduced energy consumption, fine particle size of lithium iron phosphate, and excellent normal-temperature discharge performance and low-temperature charge-discharge performance.
Description
Technical field
The present invention relates to field of lithium ion battery anode, particularly relate to the preparation method of a kind of low temp lithium ion battery LiFePO 4 of anode material/carbon composite.
Technical background
Along with the appearance of new material and the improvement of battery design technology, the range of application of lithium ion battery is constantly widened.Civil area expands to energy traffic from information industry.And in national defense and military fields, lithium ion battery then covers many arm of the services such as land, sea, air, sky.Wherein, when military equipment needs to work at Han Qu, (as less than-40 DEG C) are just high to the low temperature electrochemical performance requirement of lithium ion battery, but the charge-discharge performance decay of lithium ion battery below-20 DEG C in low temperature environment significantly, significantly limit the normal operation of corps under adverse weather condition.
Form from the structure of lithium ion battery, the performance of battery anode active material chemical property is one of important factor in order of lithium ion battery cryogenic property.Due to LiFePO
4there is the advantages such as abundant raw material source, cheap and excellent high temperature cyclic performance and security performance, LiFePO
4be suitable as very much the positive electrode of motor vehicle and all kinds of energy storage device, but its intrinsic characteristic (under room temperature its electronic conductivity and ion diffusion rates low, be respectively 10
-8-10
-10s/cm and 10
-12-10
-14cm
2/ s) cause LiFePO
4as positive electrode battery at low temperatures time charge-discharge performance have remarkable decay.At present, mainly its cryogenic property is improved from aspects such as shortening lithium ion the evolving path, Surface coating electric conducting material and doping.
Reduce LiFePO4 primary particle size, the conventional method shortening lithium ion the evolving path is generally divided into Mechanical Method and liquid phase synthesizing method.The general step of Mechanical Method is all carry out high-energy ball milling once or twice after being mixed by basic material to calcine for a long time to increase response area again, if number of patent application is for as described in 201210155024.5 and 201310504706.7, its shortcoming is a large amount of milling apparatus of needs and energy consumption is large.Conventional liquid phase synthesizing method is hydro-thermal or solvent-thermal process, as as described in Authorization Notice No. CN100454615C, the method not only needs to carry out in high pressure reactor, require higher to consersion unit, and productive rate is lower, increase cost pressure, obtained average grain diameter is that the dispersed lithium iron phosphate nanometer crystal low temperature performance of 200-500nm is not good enough.
Summary of the invention
The object of the present invention is to provide a kind of low temperature battery lithium iron phosphate/carbon composite cathode material and preparation method thereof, composite positive pole obtained by this method has higher specific capacity and good low temperature charge-discharge performance.
The preparation method of low temperature battery LiFePO 4 of anode material/carbon composite of the present invention, is characterized in that: comprise the following steps:
A. ferro-compound, lithium compound, phosphorus compound and carbon source is disperseed respectively to be formed in deionized water solution or suspension-turbid liquid that concentration is 0.5-1.5mol/L; Described ferro-compound in molar ratio: lithium compound: phosphorus compound=0.98 ~ 1:1:1 ~ 1.02; Described carbon source is 1% ~ 10% of the quality by basic material gained lithium iron phosphate positive material;
B. join in the liquid-phase reduction agent of certain volume by gained solution or suspension-turbid liquid in step a, after forming mixed solution, under uniform temperature, atmospheric pressure reflux reacts 4-16h, and then Separation of Solid and Liquid obtains ferric lithium phosphate precursor powder;
C. ferric lithium phosphate precursor powder is placed in inert atmosphere sintering furnace and is warming up to 550-750 DEG C of calcining 1-5h, after cooling, namely obtain low form lithium iron phosphate/carbon composite cathode material.
Further, described ferro-compound is one or more mixtures in ferrous acetate, ferrous carbonate, ferrous phosphate, ferrous sulfate, ferrous oxalate, frerrous chloride; Described lithium compound is one or more mixtures in lithium hydroxide, lithium carbonate, lithium acetate, lithium oxalate, lithium nitrate; One or more mixtures in described phosphorus compound organic phosphorus sources; Described carbon source is one or more mixtures in organic acid, organic carbohydrate, inorganic conductive agent;
Further, described phosphorus compound is one or more mixtures in ammonium dihydrogen phosphate, diammonium hydrogen phosphate, phosphoric acid, phytic acid; Described carbon source is one or more mixtures in citric acid, ascorbic acid, glucose, sucrose, fructose, acetylene black, carbon nano-tube, electrically conductive graphite;
Further, in step b, join in the liquid-phase reduction agent of certain volume according to following order, form mixed solution: first add ferro-compound solution or suspension-turbid liquid, then add phosphorus compound solution, then add carbon source solution or suspension-turbid liquid, finally add lithium compound solution or suspension-turbid liquid;
Further, described liquid-phase reduction agent is the mixture of one or more arbitrary proportions in ethylene glycol, diethylene glycol (DEG), triethylene glycol, tetraethylene glycol, methyl-sulfoxide, glycerol, oleyl amine; The volume ratio of liquid-phase reduction agent and deionized water is: liquid-phase reduction agent: deionized water=1:0.2 ~ 5;
Further, in step b, reaction temperature is 150 DEG C of boiling temperatures to liquid-phase reduction agent;
Further, described Separation of Solid and Liquid comprises centrifugation step, decompression distillation step, filtration step;
Further, in step c, the heating rate in calcination process is 2 ~ 5 DEG C/min;
Further, described ferro-compound in molar ratio: lithium compound: phosphorus compound=1.0:1.0:1.0 disperses the ferrous phosphate turbid liquid concentration formed afterwards in deionized water to be 1.5mol/L respectively, and the concentration of lithium hydroxide, phosphoric acid, citric acid solution is respectively 1.0mol/L, 0.5mol/L, 0.5mol/L;
The present invention also discloses a kind of low form lithium iron phosphate/carbon composite cathode material, and described composite positive pole is obtained by the preparation method of above-mentioned low temperature battery LiFePO 4 of anode material/carbon composite.
Beneficial effect of the present invention: the preparation method of low temperature battery LiFePO 4 of anode material/carbon composite of the present invention, synthesis technique is simple, and without the need to high energy milling equipment and high pressure reactor, process conditions are gentle, raw material sources are extensive, greatly reduce energy consumption and production cost; The strongly reducing atmosphere utilizing liquid-phase reduction agent to provide, prevents ferrous oxidation; Presoma crystallization is more complete, shortens the high-temperature calcination time, stops the reduction of growing up, promoting energy consumption of particle further; Realize in-situ carbon coated, LiFePO4 particle diameter is little, under normal temperature 0.1C first discharge capacity be greater than 150, at-20 DEG C, capability retention is 70%.
Accompanying drawing explanation
Below in conjunction with the drawings and specific embodiments to further instruction of the present invention.
Fig. 1 is the SEM figure of lithium ion cell positive lithium iron phosphate/carbon composite material prepared by embodiment 1;
Fig. 2 is the XRD figure of lithium ion cell positive lithium iron phosphate/carbon composite material prepared by embodiment 1;
Fig. 3 is lithium ion cell positive lithium iron phosphate/carbon composite material room temperature capacity curve prepared by embodiment 1
Fig. 4 is-20 DEG C of test curves of lithium ion cell positive lithium iron phosphate/carbon composite material prepared by embodiment 1;
Embodiment
The preparation method of the low temperature battery LiFePO 4 of anode material/carbon composite of the present embodiment, is characterized in that: comprise the following steps:
A. ferro-compound, lithium compound, phosphorus compound and carbon source is disperseed respectively to be formed in deionized water solution or suspension-turbid liquid that concentration is 0.5-1.5mol/L; Described ferro-compound in molar ratio: lithium compound: phosphorus compound=0.98 ~ 1:1:1 ~ 1.02; Described carbon source is 1% ~ 10% of the quality by basic material gained lithium iron phosphate positive material;
B. join in the liquid-phase reduction agent of certain volume by gained solution or suspension-turbid liquid in step a, after forming mixed solution, under uniform temperature, atmospheric pressure reflux reacts 4-16h, and then Separation of Solid and Liquid obtains ferric lithium phosphate precursor powder;
C. ferric lithium phosphate precursor powder is placed in inert atmosphere sintering furnace and is warming up to 550-750 DEG C of calcining 1-5h, after cooling, namely obtain low form lithium iron phosphate/carbon composite cathode material.
In the present embodiment, described ferro-compound is one or more mixtures in ferrous acetate, ferrous carbonate, ferrous phosphate, ferrous sulfate, ferrous oxalate, frerrous chloride; Described lithium compound is one or more mixtures in lithium hydroxide, lithium carbonate, lithium acetate, lithium oxalate, lithium nitrate; One or more mixtures in described phosphorus compound organic phosphorus sources; Described carbon source is one or more mixtures in organic acid, organic carbohydrate, inorganic conductive agent;
In the present embodiment, described phosphorus compound is one or more mixtures in ammonium dihydrogen phosphate, diammonium hydrogen phosphate, phosphoric acid, phytic acid; Described carbon source is one or more mixtures in citric acid, ascorbic acid, glucose, sucrose, fructose, acetylene black, carbon nano-tube, electrically conductive graphite;
In the present embodiment, in step b, join in the liquid-phase reduction agent of certain volume according to following order, form mixed solution: first add ferro-compound solution or suspension-turbid liquid, then add phosphorus compound solution, then add carbon source solution or suspension-turbid liquid, finally add lithium compound solution or suspension-turbid liquid;
In the present embodiment, described liquid-phase reduction agent is the mixture of one or more arbitrary proportions in ethylene glycol, diethylene glycol (DEG), triethylene glycol, tetraethylene glycol, methyl-sulfoxide, glycerol, oleyl amine; The volume ratio of liquid-phase reduction agent and deionized water is: liquid-phase reduction agent: deionized water=1:1 ~ 5;
In the present embodiment, in step b, reaction temperature is 150 DEG C of boiling temperatures to liquid-phase reduction agent;
In the present embodiment, described Separation of Solid and Liquid comprises centrifugation step, decompression distillation step, filtration step;
In the present embodiment, in step c, the heating rate in calcination process is 2 ~ 5 DEG C/min;
In the present embodiment, described ferro-compound in molar ratio: lithium compound: phosphorus compound=1.0:1.0:1.0 disperses the ferrous phosphate turbid liquid concentration formed afterwards in deionized water to be 1.5mol/L respectively, and the concentration of lithium hydroxide, phosphoric acid, citric acid solution is respectively 1.0mol/L, 0.5mol/L, 0.5mol/L;
The low form lithium iron phosphate/carbon composite cathode material of this enforcement, described composite positive pole is obtained by the preparation method of above-mentioned low temperature battery LiFePO 4 of anode material/carbon composite.
Below by specific embodiment, the present invention is further elaborated.
Embodiment 1
Take basic material ferrous phosphate according to the ratio of elemental mole ratios Fe:Li:P=1.0:1.0:1.0, lithium hydroxide and phosphoric acid, the amount taking carbon source citric acid by acquisition lithium iron phosphate positive material 10%, above-mentioned raw materials is disperseed in deionized water separately, ferrous phosphate turbid liquid concentration is 1.5mol/L, the concentration of lithium hydroxide, phosphoric acid and citric acid solution is respectively 1.0mol/L, 0.5mol/L and 0.5mol/L, the volume summation of suspension-turbid liquid and solution and the volume ratio of liquid-phase reduction agent triethylene glycol are 1.0, join in liquid-phase reduction agent according to following order, stir while adding: ferrous phosphate suspension-turbid liquid-phosphoric acid solution-citric acid solution-lithium hydroxide solution, after mixing at 250 DEG C back flow reaction 8h, carry out centrifugally operated after cooling and realize Separation of Solid and Liquid, namely course of reaction obtains the more complete ferric lithium phosphate precursor material of crystallization of Surface coating one deck conductive agent without the need to inert gas shielding, after the vacuumize of gained presoma in inert atmosphere sintering furnace with the speed that heating rate is 5 DEG C/min, 650 DEG C of insulation 2h, namely lithium iron phosphate/carbon combination electrode is obtained with after stove cooling.
SEM Fig. 1 and XRD Fig. 2 of the lithium iron phosphate/carbon combination electrode material that this embodiment obtains can find out, the average grain diameter of corynebacterium lithium iron phosphate/carbon composite material is 100-200nm, and be olivine-type orthohormbic structure, perfect crystalline is without dephasign.First charge-discharge curve under the experiment half-cell room temperature made by embodiment 1 gained positive electrode is shown in Fig. 3, and its 0.1C first discharge specific capacity is 160mAh/g as seen, and at-20 DEG C, the discharge capacity first of 0.1C is 110mAh/g.
Embodiment 2
Take basic material ferrous carbonate according to the ratio of elemental mole ratios Fe:Li:P=0.98:1.0:1.0, lithium acetate and ammonium dihydrogen phosphate, the amount taking carbon source glucose by acquisition lithium iron phosphate positive material 10%, above-mentioned raw materials is disperseed in deionized water separately, ferrous carbonate turbid liquid concentration is 1.2mol/L, the concentration of lithium acetate, ammonium dihydrogen phosphate and glucose solution is respectively 0.5mol/L, 1.0mol/L and 1.0mol/L, the volume summation of suspension-turbid liquid and solution and the volume ratio of liquid-phase reduction agent diethylene glycol (DEG) are 0.5, join in liquid-phase reduction agent according to following order, stir while adding: ferrous carbonate suspension-turbid liquid-ammonium dihydrogen phosphate-glucose solution-lithium acetate solution, after mixing at 240 DEG C back flow reaction 12h, carry out centrifugally operated after cooling and realize Separation of Solid and Liquid, namely course of reaction obtains the more complete ferric lithium phosphate precursor material of crystallization of Surface coating one deck conductive agent without the need to inert gas shielding, after the vacuumize of gained presoma in inert atmosphere sintering furnace with the speed that heating rate is 4 DEG C/min, 700 DEG C of insulation 2h, namely lithium iron phosphate/carbon combination electrode is obtained with after stove cooling.
The surface sweeping electromicroscopic photograph of the lithium iron phosphate/carbon combination electrode material that this embodiment obtains as shown in Figure 1, therefrom the XRD figure of lithium iron phosphate/carbon composite material, first charge-discharge curve chart under room temperature and low temperature and Fig. 2 to Fig. 4 without essential distinction, repeat no more herein.Room temperature 0.1C first charge-discharge capacity is 158mAh/g, at-20 DEG C 0.1C first discharge capacity be 109mAh/g.
Embodiment 3
Take basic material ferrous oxalate according to the ratio of elemental mole ratios Fe:Li:P=1.0:1.02:1.0, careless lithium and phosphoric acid, the amount taking carbon source sucrose by acquisition lithium iron phosphate positive material 8%, above-mentioned raw materials is disperseed in deionized water separately, ferrous oxalate turbid liquid concentration is 1.0mol/L, the concentration of lithium oxalate, phosphoric acid and sucrose solution is respectively 1.5mol/L, 1.0mol/L and 1.0mol/L, and the volume summation of suspension-turbid liquid and solution and the volume ratio of liquid-phase reduction agent ethylene glycol are 0.5, join in liquid-phase reduction agent according to following order, stir while adding: ferrous oxalate suspension-turbid liquid-phosphoric acid solution-sucrose solution-lithium oxalate solution, after mixing at 180 DEG C back flow reaction 14h, carry out centrifugally operated after cooling and realize Separation of Solid and Liquid, namely course of reaction obtains the more complete ferric lithium phosphate precursor material of crystallization of Surface coating one deck conductive agent without the need to inert gas shielding, after the vacuumize of gained presoma in inert atmosphere sintering furnace with the speed that heating rate is 3 DEG C/min, 750 DEG C of insulation 2h, namely lithium iron phosphate/carbon combination electrode is obtained with after stove cooling.
The surface sweeping electromicroscopic photograph of the lithium iron phosphate/carbon combination electrode material that this embodiment obtains as shown in Figure 1, therefrom the XRD figure of lithium iron phosphate/carbon composite material, first charge-discharge curve chart under room temperature and low temperature and Fig. 2 to Fig. 4 without essential distinction, repeat no more herein.Room temperature 0.1C first charge-discharge capacity is 155mAh/g, at-20 DEG C 0.1C first discharge capacity be 109mAh/g.
Embodiment 4
Take basic material ferrous sulfate according to the ratio of elemental mole ratios Fe:Li:P=0.98:1.2:1.0, lithium carbonate and phytic acid, the amount taking conductive agent acetylene black by acquisition lithium iron phosphate positive material 3%, above-mentioned raw materials is disperseed in deionized water separately, copperas solution concentration is 2.0mol/L, the concentration of lithium carbonate suspension-turbid liquid, phytic acid and acetylene black suspension-turbid liquid is respectively 0.5mol/L, 1.0mol/L and 1.0mol/L, the volume summation of suspension-turbid liquid and solution and the volume ratio of liquid-phase reduction agent triethylene glycol are 2.0, join in liquid-phase reduction agent according to following order, stir while adding: copperas solution-plant acid solution-acetylene black suspension-turbid liquid-lithium carbonate suspension-turbid liquid, after mixing at 280 DEG C back flow reaction 16h, carry out centrifugally operated after cooling and realize Separation of Solid and Liquid, namely course of reaction obtains the more complete ferric lithium phosphate precursor material of crystallization of Surface coating one deck conductive agent without the need to inert gas shielding, after the vacuumize of gained presoma in inert atmosphere sintering furnace with the speed that heating rate is 2 DEG C/min, 650 DEG C of insulation 2h, namely lithium iron phosphate/carbon combination electrode is obtained with after stove cooling.
The surface sweeping electromicroscopic photograph of the lithium iron phosphate/carbon combination electrode material that this embodiment obtains as shown in Figure 1, therefrom the XRD figure of lithium iron phosphate/carbon composite material, first charge-discharge curve chart under room temperature and low temperature and Fig. 2 to Fig. 4 without essential distinction, repeat no more herein.Room temperature 0.1C first charge-discharge capacity is 155mAh/g, at-20 DEG C 0.1C first discharge capacity be 108mAh/g.
What finally illustrate is, above embodiment is only in order to illustrate technical scheme of the present invention and unrestricted, although with reference to preferred embodiment to invention has been detailed description, those of ordinary skill in the art is to be understood that, can modify to technical scheme of the present invention or equivalent replacement, and not departing from aim and the scope of technical solution of the present invention, it all should be encompassed in the middle of right of the present invention.
Claims (10)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201410667397.XA CN104393293A (en) | 2014-11-20 | 2014-11-20 | Positive pole lithium iron phosphate/carbon composite material for low-temperature battery and preparation method of composite material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201410667397.XA CN104393293A (en) | 2014-11-20 | 2014-11-20 | Positive pole lithium iron phosphate/carbon composite material for low-temperature battery and preparation method of composite material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN104393293A true CN104393293A (en) | 2015-03-04 |
Family
ID=52611157
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201410667397.XA Pending CN104393293A (en) | 2014-11-20 | 2014-11-20 | Positive pole lithium iron phosphate/carbon composite material for low-temperature battery and preparation method of composite material |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN104393293A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106129337A (en) * | 2016-06-27 | 2016-11-16 | 华中农业大学 | A kind of preparation method of cathode of lithium iron phosphate lithium ion battery electrode |
| CN109904409A (en) * | 2019-01-14 | 2019-06-18 | 广东工业大学 | A kind of lithium iron phosphate nanorod/graphene composite material and preparation method and application thereof |
| CN110350191A (en) * | 2019-07-12 | 2019-10-18 | 西南大学 | Sodium/lithium ion battery phosphate cathode material preparation method |
| CN111916725A (en) * | 2019-05-08 | 2020-11-10 | 中国石油化工股份有限公司 | Phosphorus-doped lithium battery high-nickel positive electrode material and preparation process thereof |
| CN113321198A (en) * | 2021-05-28 | 2021-08-31 | 西南大学 | Binary metal phosphate anode material and preparation method and application thereof |
| CN113942988A (en) * | 2021-11-22 | 2022-01-18 | 青岛九环新越新能源科技股份有限公司 | Iron phosphate and preparation method thereof |
| CN114084879A (en) * | 2021-11-22 | 2022-02-25 | 青岛九环新越新能源科技股份有限公司 | Lithium iron phosphate and production method and application thereof |
| CN115321508A (en) * | 2022-09-06 | 2022-11-11 | 国网内蒙古东部电力有限公司通辽供电公司 | Positive electrode porous lithium iron phosphate material for low temperature battery and preparation method thereof |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7390473B1 (en) * | 2002-10-29 | 2008-06-24 | Nei Corp. | Method of making fine lithium iron phosphate/carbon-based powders with an olivine type structure |
| CN102447108A (en) * | 2011-11-02 | 2012-05-09 | 宁波大学 | Preparation method of lithium iron phosphate/carbon composite cathode material of lithium ion battery |
| CN103427079A (en) * | 2013-08-09 | 2013-12-04 | 中物院成都科学技术发展中心 | Preparation method of lithium ion phosphate/carbon composite material for high-rate-capability lithium ion battery |
-
2014
- 2014-11-20 CN CN201410667397.XA patent/CN104393293A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7390473B1 (en) * | 2002-10-29 | 2008-06-24 | Nei Corp. | Method of making fine lithium iron phosphate/carbon-based powders with an olivine type structure |
| CN102447108A (en) * | 2011-11-02 | 2012-05-09 | 宁波大学 | Preparation method of lithium iron phosphate/carbon composite cathode material of lithium ion battery |
| CN103427079A (en) * | 2013-08-09 | 2013-12-04 | 中物院成都科学技术发展中心 | Preparation method of lithium ion phosphate/carbon composite material for high-rate-capability lithium ion battery |
Non-Patent Citations (1)
| Title |
|---|
| 李绍敏等: "液相沉淀-多元醇还原法合成LiFePO4/C正极材料的电化学性能", 《中国有色金属学报》, vol. 22, no. 5, 31 May 2012 (2012-05-31), pages 1311 - 1318 * |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106129337B (en) * | 2016-06-27 | 2018-10-12 | 华中农业大学 | A kind of preparation method of cathode of lithium iron phosphate lithium ion battery electrode |
| CN106129337A (en) * | 2016-06-27 | 2016-11-16 | 华中农业大学 | A kind of preparation method of cathode of lithium iron phosphate lithium ion battery electrode |
| CN109904409A (en) * | 2019-01-14 | 2019-06-18 | 广东工业大学 | A kind of lithium iron phosphate nanorod/graphene composite material and preparation method and application thereof |
| CN111916725A (en) * | 2019-05-08 | 2020-11-10 | 中国石油化工股份有限公司 | Phosphorus-doped lithium battery high-nickel positive electrode material and preparation process thereof |
| CN111916725B (en) * | 2019-05-08 | 2023-05-02 | 中国石油化工股份有限公司 | Phosphorus-doped high-nickel cathode material for lithium battery and preparation process thereof |
| CN110350191A (en) * | 2019-07-12 | 2019-10-18 | 西南大学 | Sodium/lithium ion battery phosphate cathode material preparation method |
| CN113321198B (en) * | 2021-05-28 | 2022-03-01 | 西南大学 | Binary metal phosphate cathode material, preparation method and application thereof |
| CN113321198A (en) * | 2021-05-28 | 2021-08-31 | 西南大学 | Binary metal phosphate anode material and preparation method and application thereof |
| CN113942988A (en) * | 2021-11-22 | 2022-01-18 | 青岛九环新越新能源科技股份有限公司 | Iron phosphate and preparation method thereof |
| CN114084879A (en) * | 2021-11-22 | 2022-02-25 | 青岛九环新越新能源科技股份有限公司 | Lithium iron phosphate and production method and application thereof |
| CN114084879B (en) * | 2021-11-22 | 2023-09-12 | 青岛九环新越新能源科技股份有限公司 | Lithium iron phosphate and production method and application thereof |
| CN113942988B (en) * | 2021-11-22 | 2023-09-12 | 青岛九环新越新能源科技股份有限公司 | Ferric phosphate and preparation method thereof |
| CN115321508A (en) * | 2022-09-06 | 2022-11-11 | 国网内蒙古东部电力有限公司通辽供电公司 | Positive electrode porous lithium iron phosphate material for low temperature battery and preparation method thereof |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN104393293A (en) | Positive pole lithium iron phosphate/carbon composite material for low-temperature battery and preparation method of composite material | |
| CN103840157B (en) | A kind of preparation method of nano-sheet lithium ion battery anode material vanadium lithium phosphate | |
| CN102569794B (en) | Carbon-coating method for lithium iron phosphate anode material | |
| CN109860572A (en) | The preparation method of the compound carbon-coated nano-scale lithium iron phosphate of three-dimensional net structure | |
| CN109607505A (en) | A kind of preparation method for the LiFePO4 improving cryogenic property | |
| CN106450239B (en) | A kind of iron manganese phosphate for lithium composite material and preparation method and lithium ion battery | |
| CN109817904B (en) | High-voltage long-cycle high-nickel single crystal positive electrode material and preparation method and application thereof | |
| CN101339991B (en) | Composite coating modified high tap density lithium ion battery positive electrode material and its preparation method and application | |
| CN103545522A (en) | Preparation method of positive electrode active material for lithium ion battery | |
| CN109860526B (en) | Preparation method of graphite material doped with metal oxalate lithium battery composite negative electrode material | |
| CN108448113B (en) | Preparation method of doped modified lithium iron phosphate positive-grade material | |
| CN103078113A (en) | Vanadium-titanium ion-codoped lithium iron phosphate material and preparation method thereof | |
| CN110611080A (en) | A transition metal-doped sodium titanomanganese phosphate/carbon composite positive electrode material and its preparation and application in sodium-ion batteries | |
| CN111180709A (en) | Carbon nanotube and metal copper co-doped lithium ferrous oxalate battery composite negative electrode material and preparation method thereof | |
| CN108899505A (en) | Fluorophosphoric acid vanadium sodium positive electrode of doping vario-property and preparation method thereof | |
| CN103427079A (en) | Preparation method of lithium ion phosphate/carbon composite material for high-rate-capability lithium ion battery | |
| CN107978738A (en) | A kind of composite positive pole of manganese pyrophosphate sodium/carbon and its preparation and application | |
| CN102623705A (en) | Lithium ion battery cathode material LiFePO4/C, and preparation method and application thereof | |
| CN102299317A (en) | High-rate LiFePO4/mesoporous carbon composite cathode material and preparation method thereof | |
| CN103413944A (en) | Lithium manganese phosphate positive electrode material and preparation method thereof | |
| CN100490221C (en) | Composite doped modified lithium-ion battery anode material and its manufacture method | |
| CN116741975A (en) | Double-carbon-layer heterogeneous composite positive electrode material, preparation method thereof and sodium ion battery | |
| CN103693632B (en) | A kind of preparation method of lithium vanadyl phosphate positive material for lithium ion battery | |
| CN110085854B (en) | Lithium vanadium phosphate cathode material and preparation method thereof | |
| CN112186151A (en) | Cobalt phosphide nanoparticle inlaid carbon nanosheet array material and preparation and application thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| RJ01 | Rejection of invention patent application after publication | ||
| RJ01 | Rejection of invention patent application after publication |
Application publication date: 20150304 |