CN1958440A - Method for synthesizing Nano level powder of lithium iron phosphate - Google Patents
Method for synthesizing Nano level powder of lithium iron phosphate Download PDFInfo
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- CN1958440A CN1958440A CNA2006101367371A CN200610136737A CN1958440A CN 1958440 A CN1958440 A CN 1958440A CN A2006101367371 A CNA2006101367371 A CN A2006101367371A CN 200610136737 A CN200610136737 A CN 200610136737A CN 1958440 A CN1958440 A CN 1958440A
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Abstract
This invention relates to a quenching method for preparing nanoscale anode material lithium iron phosphate for lithium-ion batteries. The method comprises: mixing lithium salt, iron salt, phosphate, organic precursor of carbon, and doping metal ions by high energy ball milling, oven-drying, loading into an inert atmosphere furnace, reacting at 300-400 deg.C for 2-6 h, cooling to room temperature, taking out the powder, pressing into block, loading into a stainless steel container, vacuumizing, sealing, placing the sealed stainless steel container into a muffle furnace, calcining, taking out the stainless steel container at the calcining temperature, and quenching to obtain nanoscale anode material lithium iron phosphate, which has such advantages as high electronic-ionic conductivity and excellent electrochemical properties.
Description
Technical field the invention belongs to a kind of preparation method of nano-scale lithium ion battery anode material, particularly a kind of method that adopts the LiFePO 4 of anode material of the synthetic high electron-ion electroconductibility of quenching method.
The LiFePO of background technology olivine structural
4Have raw material sources extensive, cheap, as the anode material for lithium-ion batteries high-temperature behavior good and by the people for being a kind of comparatively ideal lithium ion secondary power battery anode material.But, LiFePO
4Have the shortcoming of electron-ion poorly conductive, thus improve its electron-ion electroconductibility be iron lithium phosphate application-oriented the problem that must solve.
At present synthetic LiFePO
4Method mainly contain high temperature solid-state method, hydrothermal method, sol-gel method, liquid-phase oxidation reduction method, solid phase microwave method.
The high temperature solid-state method that is widely adopted at present is with ferrous oxalate or acetate, mixes with ammonium hydrogen phosphate and lithium salts, obtains product through high-temperature calcination then under inert atmosphere argon gas or nitrogen protection.The crystal grain of this method synthetic iron lithium phosphate is thick, the ion-electron poorly conductive of material.
Carbothermic method also is a kind of in the high temperature solid-state method, and generally adopting ferric oxide or Z 250 is source of iron, and under high temperature and argon gas or nitrogen protection, carbon is reduced to ferrous iron with ferric iron.Long and problem that excessive grain is grown up still exists for this method reaction times, thereby is difficult to prepare the good positive electrode material of chemical property.
Though hydrothermal method can prepare the high lithium iron phosphate positive material of nano level electron-ion electroconductibility, hydrothermal method will be used the reactor of high temperature high voltage resistant, and often there is the also very difficult control of preparation process in final product with dephasign.
Sol-gel method presoma dry shrinkage is big, the suitability for industrialized production difficulty is big, synthesis cycle is longer.Metal alkoxide costs an arm and a leg in addition, and the solvent of alkoxide is poisonous usually.
Vitamins C acid, H have been used in the liquid-phase oxidation method of reducing
2O
2, LiI, etc. Chemicals, thereby increased the cost of product and the complicacy of technology, therefore also be not suitable for industrial production.
Summary of the invention is at the disadvantage of iron lithium phosphate ion-electron poorly conductive, the present invention with the iron lithium phosphate for preparing high electron-ion electroconductibility with nano-scale as target and proposed a kind of method preparing phosphate iron lithium, this method adopts the quenching technology to prepare nano-scale lithium iron phosphate, can prepare the electrode materials of high electron-ion electroconductibility, chemical property is good.
The way that the present invention prepares lithium iron phosphate positive material is as follows:
A kind of method of synthesizing Nano level powder of lithium iron phosphate, adopting lithium salts, molysite, phosphoric acid salt, doped element and conductive agent is raw material, with lithium salts, molysite, doped metal ion (Me
N+) and phosphoric acid salt according to mol ratio be: lithium: iron: Me
N+: phosphatase 11 .0: x (x=0.80-0.99): (1-x): 1.0, add the conductive agent of above-mentioned raw materials total mass 0.5-2.0% simultaneously; The process ball milling mixes and is placed in the inert atmosphere Reaktionsofen, and temperature of reaction is 300-400 ℃, and soaking time is 2-6 hour, is cooled to room temperature then; With powder taking-up, briquetting, again the block presoma is placed in the heat-resistance stainless steel container, vacuumize sealing, place in the retort furnace through 500-800 ℃ of calcining, calcination time is 10-20 hour, in calcining temperature quenching is carried out in the heat-resistance stainless steel container taking-up of sealing then, obtain the Nano level powder of lithium iron phosphate material behind the quenching.
Described lithium salts comprises: one or more in Quilonum Retard, lithium hydroxide, lithium nitrate, lithium chloride, the monometallic;
Described molysite comprises: one or more in Ferrox, ferric oxide, ferrous sulfate, the tertiary iron phosphate;
Described phosphoric acid salt comprises: one or more in ammonium hydrogen phosphate, primary ammonium phosphate, tertiary iron phosphate, the monometallic;
Described doped element is one or more in the elements such as manganese, zinc, titanium, magnesium, aluminium, zirconium, niobium, chromium and rare earth,
Described conductive agent is the presoma of carbon or carbon, comprises in acetylene black, crystalline flake graphite, sucrose, glucose, the polyvinyl alcohol one or more.
The present invention falls by product by a low temperature 300-400 ℃ calcining and decomposing, again the gained presoma is carried out the tap density that briquetting can significantly improve product; The quenching technology is applied to the present invention, it is short to have temperature fall time, the characteristics that synthesis temperature is low, and the iron lithium phosphate product purity height of preparation, carbon content is low, chemical property and physicals are good, adopt quenching technology synthetic material and have the grain-size of nano-scale, electron-ion electroconductibility height.
Adopt the iron lithium phosphate of the nano-scale of the present invention's preparation can reduce the evolving path of lithium ion effectively at electrode process, because particle is tiny thereby can be so that material and electrolytic solution fully contact the utilization ratio of raising active substance, can improve the intrinsic conductivity of this material and improve the interfacial charge transmission capacity that electrode-electric is separated liquid by bulk phase-doped and surperficial coating, loading capacity reaches 155mAh/g first, and the prepared iron lithium phosphate of traditional high temperature solid-state method under the 0.2C multiplying power first loading capacity have only 110mAh/g.
Description of drawings
Fig. 1: the SEM of sample figure, A-embodiment 1 gained sample wherein, B-embodiment 2 gained samples, C-embodiment 3 gained samples;
Fig. 2: the XRD figure of sample, A-embodiment 1 gained sample wherein, B-embodiment 2 gained samples, C-embodiment 3 gained samples;
Fig. 3: the charging and discharging curve-voltage pattern of sample, A-embodiment 1 gained sample wherein, B-embodiment 2 gained samples, C-embodiment 3 gained samples.
Embodiment
Embodiment 1: with lithium carbonate containing 3.71 grams; Ferrox 18 grams; the mixture of NiO 0.37 gram primary ammonium phosphate 11.52 gram sucrose 1.2 grams is through high-energy ball milling; place homemade inert atmosphere Reaktionsofen through 60 ℃ of oven dry of low temperature; begin to heat up, temperature of reaction is that 300-400 ℃ of soaking time is 4 hours, decomposes and discharges by product; be cooled to room temperature then, feed rare gas element in the whole process and protect.With powder taking-up, briquetting, again the block presoma is placed in the heat-resistance stainless steel container, vacuumize sealing.The heat-resistance stainless steel container of sealing is placed in the retort furnace through 650 ℃ of calcining certain hours, in calcining temperature the heat-resistance stainless steel container of sealing is taken out then and carry out quenching, product is taken out the Nano level powder of lithium iron phosphate material of the nickel ion that just obtains mixing.The specific storage of Zhi Bei material is 155mAh/g after testing.Embodiment 2: with lithium carbonate containing 3.71 grams, and Ferrox 18 grams, MnCO
30.114 the mixture of gram primary ammonium phosphate 11.52 gram sucrose 1.2 grams is through high-energy ball milling; place homemade inert atmosphere Reaktionsofen through 60 ℃ of oven dry of low temperature; begin to heat up; temperature of reaction is that 300-400 ℃ of soaking time is 4 hours; decompose and discharge by product; be cooled to room temperature then, feed rare gas element in the whole process and protect.With powder taking-up, briquetting, again the block presoma is placed in the heat-resistance stainless steel container, vacuumize sealing.The heat-resistance stainless steel container of sealing is placed in the retort furnace through 650 ℃ of calcining certain hours, in calcining temperature the heat-resistance stainless steel container of sealing is taken out then and carry out quenching, product is taken out just obtain doped with manganese ionic Nano level powder of lithium iron phosphate material.The specific storage of Zhi Bei material is 149mAh/g after testing.
Embodiment 3: with lithium carbonate containing 3.71 grams, and Ferrox 18 grams, CoCO
30.236 the mixture of gram primary ammonium phosphate 11.52 gram sucrose 1.2 grams is through high-energy ball milling; place homemade inert atmosphere Reaktionsofen through 60 ℃ of oven dry of low temperature; begin to heat up; temperature of reaction is that 300-400 ℃ of soaking time is 4 hours; decompose and discharge by product; be cooled to room temperature then, feed rare gas element in the whole process and protect.With powder taking-up, briquetting, again the block presoma is placed in the heat-resistance stainless steel container, vacuumize sealing.The heat-resistance stainless steel container of sealing is placed in the retort furnace through 650 ℃ of calcining certain hours, in calcining temperature the heat-resistance stainless steel container of sealing is taken out then and carry out quenching, product is taken out the Nano level powder of lithium iron phosphate material of the cobalt that just obtains mixing.The specific storage of Zhi Bei material is 145mAh/g after testing.
Claims (6)
1. the method for a synthesizing Nano level powder of lithium iron phosphate is characterized in that: adopting lithium salts, molysite, phosphoric acid salt, doped element and conductive agent is raw material, with lithium salts, molysite, doped metal ion and phosphoric acid salt according to the mol ratio lithium: iron: Me
N+: phosphoric acid is 1.0: x: (1-x): 1.0, and x=0.80-0.99 wherein adds the conductive agent of above-mentioned raw materials total mass 0.5-2.0% simultaneously; The process ball milling mixes and is placed in the inert atmosphere Reaktionsofen, and temperature of reaction is 300-400 ℃, and soaking time is 2-6 hour, is cooled to room temperature then; With powder taking-up, briquetting, again the block presoma is placed in the heat-resistance stainless steel container, vacuumize sealing, place in the retort furnace through 500-800 ℃ of calcining, calcination time is 10-20 hour, in calcining temperature quenching is carried out in the heat-resistance stainless steel container taking-up of sealing then, obtain the Nano level powder of lithium iron phosphate material behind the quenching.
2. according to the preparation method of the described LiFePO 4 powder of claim 1, it is characterized in that: described lithium salts comprises: one or more in Quilonum Retard, lithium hydroxide, lithium nitrate, lithium chloride, the monometallic.
3. according to the preparation method of the described LiFePO 4 powder of claim 1, it is characterized in that: described molysite comprises: one or more in Ferrox, ferric oxide, ferrous sulfate, the tertiary iron phosphate.
4. according to the preparation method of the described LiFePO 4 powder of claim 1, it is characterized in that: described phosphoric acid salt comprises: one or more in ammonium hydrogen phosphate, primary ammonium phosphate, tertiary iron phosphate, the monometallic.
5. according to the preparation method of the described LiFePO 4 powder of claim 1, it is characterized in that: described doped element is one or more in the elements such as manganese, zinc, titanium, magnesium, aluminium, zirconium, niobium, chromium and rare earth.
6. according to the preparation method of the described LiFePO 4 powder of claim 1, it is characterized in that: described conductive agent is the presoma of carbon or carbon, comprises in acetylene black, crystalline flake graphite, sucrose, glucose, the polyvinyl alcohol one or more.
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| CN101800310A (en) * | 2010-04-02 | 2010-08-11 | 中国科学院苏州纳米技术与纳米仿生研究所 | Method for preparing graphene-doped anode material for lithium-ion batteries |
| CN102013489A (en) * | 2010-10-28 | 2011-04-13 | 河北工业大学 | Metallic titanium doped carbon-coating lithium iron phosphate and preparation method thereof |
| CN102064317A (en) * | 2009-11-13 | 2011-05-18 | 深圳市比克电池有限公司 | LiFe1-xMxPO4 compound containing carbon element and preparation method thereof |
| CN101359731B (en) * | 2007-07-31 | 2012-03-14 | 深圳市比克电池有限公司 | Method for synthesizing lithium ionic cell positive pole material lithium iron phosphate |
| CN102502562A (en) * | 2011-11-14 | 2012-06-20 | 东莞市长安东阳光铝业研发有限公司 | Preparation method of lithium iron phosphate, lithium ion battery and anode material and anode thereof |
| CN102593447A (en) * | 2011-03-23 | 2012-07-18 | 江苏菲思特新能源有限公司 | Metal doping method of lithium iron phosphate anode material |
| CN101373831B (en) * | 2007-08-24 | 2012-07-25 | 比克国际(天津)有限公司 | Method for preparing lithium ion battery anode material lithium iron phosphate |
| CN102810670A (en) * | 2012-08-01 | 2012-12-05 | 因迪能源（苏州）有限公司 | Composite anode material of lithium ion battery and preparation method |
| CN108199041A (en) * | 2017-12-29 | 2018-06-22 | 桑德集团有限公司 | A kind of modified phosphate iron lithium material, preparation method and application |
| WO2018129883A1 (en) * | 2017-01-11 | 2018-07-19 | 宁德时代新能源科技股份有限公司 | Lithium iron phosphate/carbon composite material and preparation method therefor |
| CN113363483A (en) * | 2021-04-27 | 2021-09-07 | 北京当升材料科技股份有限公司 | Olivine-structure positive electrode material, preparation method and application thereof, and lithium ion battery |
| CN114188519A (en) * | 2021-12-09 | 2022-03-15 | 合肥工业大学 | Preparation method and energy storage application of nano spherical carbon-coated lithium iron phosphate composite material |
| CN114368736A (en) * | 2022-01-28 | 2022-04-19 | 中南大学 | Preparation method of olivine type sodium iron phosphate cathode material |
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| CN100418255C (en) * | 2005-12-23 | 2008-09-10 | 清华大学 | Method for preparing lithium enriched lithium ion phosphate powder |
| CN100551821C (en) * | 2005-12-23 | 2009-10-21 | 清华大学 | The preparation method of rare earth doped iron lithium phosphate powder |
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- 2006-11-24 CN CNB2006101367371A patent/CN100450919C/en not_active Expired - Fee Related
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| CN101359731B (en) * | 2007-07-31 | 2012-03-14 | 深圳市比克电池有限公司 | Method for synthesizing lithium ionic cell positive pole material lithium iron phosphate |
| CN101373831B (en) * | 2007-08-24 | 2012-07-25 | 比克国际(天津)有限公司 | Method for preparing lithium ion battery anode material lithium iron phosphate |
| CN102064317A (en) * | 2009-11-13 | 2011-05-18 | 深圳市比克电池有限公司 | LiFe1-xMxPO4 compound containing carbon element and preparation method thereof |
| CN102064317B (en) * | 2009-11-13 | 2014-11-19 | 深圳市比克电池有限公司 | LiFe1-xMxPO4 compound containing carbon element and preparation method thereof |
| CN101800310B (en) * | 2010-04-02 | 2013-02-13 | 中国科学院苏州纳米技术与纳米仿生研究所 | Method for preparing graphene-doped anode material for lithium-ion batteries |
| CN101800310A (en) * | 2010-04-02 | 2010-08-11 | 中国科学院苏州纳米技术与纳米仿生研究所 | Method for preparing graphene-doped anode material for lithium-ion batteries |
| CN102013489A (en) * | 2010-10-28 | 2011-04-13 | 河北工业大学 | Metallic titanium doped carbon-coating lithium iron phosphate and preparation method thereof |
| CN102593447A (en) * | 2011-03-23 | 2012-07-18 | 江苏菲思特新能源有限公司 | Metal doping method of lithium iron phosphate anode material |
| CN102593447B (en) * | 2011-03-23 | 2016-03-16 | 江苏菲思特新能源有限公司 | A kind of metal-doped method of lithium iron phosphate positive material |
| CN102502562B (en) * | 2011-11-14 | 2014-06-11 | 东莞市长安东阳光铝业研发有限公司 | Preparation method of lithium iron phosphate, lithium ion battery and anode material and anode thereof |
| CN102502562A (en) * | 2011-11-14 | 2012-06-20 | 东莞市长安东阳光铝业研发有限公司 | Preparation method of lithium iron phosphate, lithium ion battery and anode material and anode thereof |
| CN102810670A (en) * | 2012-08-01 | 2012-12-05 | 因迪能源（苏州）有限公司 | Composite anode material of lithium ion battery and preparation method |
| CN102810670B (en) * | 2012-08-01 | 2015-03-04 | 因迪能源（苏州）有限公司 | Composite anode material of lithium ion battery and preparation method |
| WO2018129883A1 (en) * | 2017-01-11 | 2018-07-19 | 宁德时代新能源科技股份有限公司 | Lithium iron phosphate/carbon composite material and preparation method therefor |
| CN108305991A (en) * | 2017-01-11 | 2018-07-20 | 宁德时代新能源科技股份有限公司 | Lithium iron phosphate/carbon composite material and preparation method thereof |
| CN108199041A (en) * | 2017-12-29 | 2018-06-22 | 桑德集团有限公司 | A kind of modified phosphate iron lithium material, preparation method and application |
| CN108199041B (en) * | 2017-12-29 | 2020-09-08 | 桑德新能源技术开发有限公司 | Modified lithium iron phosphate material, preparation method and application |
| CN113363483A (en) * | 2021-04-27 | 2021-09-07 | 北京当升材料科技股份有限公司 | Olivine-structure positive electrode material, preparation method and application thereof, and lithium ion battery |
| CN114188519A (en) * | 2021-12-09 | 2022-03-15 | 合肥工业大学 | Preparation method and energy storage application of nano spherical carbon-coated lithium iron phosphate composite material |
| CN114368736A (en) * | 2022-01-28 | 2022-04-19 | 中南大学 | Preparation method of olivine type sodium iron phosphate cathode material |
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