CN100399608C - Olivine carbon bobbles composite material and use thereof - Google Patents
Olivine carbon bobbles composite material and use thereof Download PDFInfo
- Publication number
- CN100399608C CN100399608C CNB2005100797645A CN200510079764A CN100399608C CN 100399608 C CN100399608 C CN 100399608C CN B2005100797645 A CNB2005100797645 A CN B2005100797645A CN 200510079764 A CN200510079764 A CN 200510079764A CN 100399608 C CN100399608 C CN 100399608C
- Authority
- CN
- China
- Prior art keywords
- carbon
- olivine
- composite material
- bobbles
- matrix
- 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.)
- Active
Links
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
Abstract
The present invention relates to a olivine carbon wool ball composite material. It one olivine basal body and wheresoever grown carbon nanotube or/and nano fiber, wherein the particle average diameter of said olivine basal body being 50 nm-50 micrometer, chemical constitution: LixAaMmBbPOzNn, said carbon nanotube or nano fiber diameter being 1-200 nm, length being 50 nm-100 um. Said composite material also includes olivine basal body surface covered single-layer carbon with thickeness 2-100 nm, carbon content being 1-20 wt per cent of basal body weight. Said composite material can directly be used as positive electrode active material in secondary lithium battery, also used as additive mixing use with existing positive electrode material. Said composite material can raise current positive electrode material and battery multiplying factor and safety feature. Secondary lithium battery Containing said olivine carbon wool composite material has large power density and high security etc advantages.
Description
Technical field
The present invention relates to a kind of positive electrode of serondary lithium battery, specifically relate to the olivine carbon bobbles composite material that a kind of basis material by olivine structural and carbon nano-tube and nanofiber are formed, and be used for the purposes of the positive electrode of serondary lithium battery.
Background technology
Transition metal phosphoric acid lithium salts (LiMPO with olivine structural
4, M=Fe, Co, Mn Ni) is a kind of positive electrode active materials that is mainly used in serondary lithium battery.It is cheap to have the prices of raw and semifnished materials, and storage is abundant, environmentally safe, and chemical property is stable, and when serondary lithium battery was used, security performance was very good, and lithium storage content is higher, and voltage is than advantages such as height.That performance is best in present this series material is iron lithium phosphate (LiFePO
4).After the development LiMPO that mix in the position and phosphate potential is alternative that taps a blast furnace again
4The shortcoming of this class material is that electronic conductivity and ionic conductivity are low.As the positive electrode active materials of serondary lithium battery, the multiplying power property of battery is relatively poor.That is to say that battery is when high current charge-discharge, battery capacity obviously reduces (for example, less than 70%) when charging and discharging with respect to little electric current.In order to address these problems, often adopted at LiMPO
4The method of coated with carbon or plated metal is improved the electronics contact between the particle, perhaps attempt to improve the intrinsic electronic conductance of material in the method for Li position doping high valence ion, perhaps improve its electronic conductance and ionic conductance in lithium position and iron position doping low price metal, perhaps replace oxygen, perhaps form intrinsic electronic conductance and ionic conductance that material is improved in the oxygen room with nitrogen.
Electrically contact the aspect from raising, the method that adopts mainly is at surface deposition or coats one deck carbon at present, further adds conductive additive such as carbon black when the preparation electrode again, and acetylene black waits to improve and electrically contacts.Because the black carbon surface as conductive additive can deposit nonconducting material in charge and discharge process, therefore in charge and discharge process, the continuous circulation along with battery can't remain good electrical contact between the active particle.
Recently, the someone proposes at LiCoO
2Deng the carbon fiber or the carbon nano-tube of adding conduction in the positive electrode, wish that carbon fiber or carbon nano-tube can form continuous conductive network.But in actual Composite Preparation process,, be difficult to its and positive electrode are evenly disperseed because the raw material of carbon nano-tube or nanofiber are generally aggregate, make it with active particle between contact well, and the phase lap is tied the formation contiguous network.
In ultra high power serondary lithium battery repid discharge process, we discover, on the one hand, the electronics contact that remains between the particle, active material have high intrinsic electronics and ionic conductance very important, on the other hand, the infiltration degree of electrolyte and electrode material surface, ion is in the transmission rate on active material surface, also the performance that discharges and recharges of appreciable impact high power.Present material modification is not also paid close attention to these problems, does not propose solution yet.So just limit the application of this material in the high power electrokinetic cell, do not given full play to the advantage of olivine class positive electrode.
Summary of the invention
The objective of the invention is in order to overcome existing olivine structural LiMPO
4The class material can not remain the good electron contact during as the positive electrode of serondary lithium battery, and the shortcoming of interface ion transport property difference; Be difficult for the shortcoming of disperseing when simultaneously in positive electrode, directly adding conductive carbon nanotube or nanofiber, thereby provide that a kind of ion transfer character is good, olivine carbon bobbles composite material that carbon nano-tube wherein or nanofiber are difficult for reunion.
The objective of the invention is to realize by the following technical solutions:
The invention provides a kind of olivine carbon bobbles composite material, comprise an olivine matrix; It is characterized in that: direct growth has carbon nano-tube or/and nanofiber on described olivine matrix, and described carbon nano-tube or nanofiber diameter are 1～200nm, and length is 50nm～100um.
Also be included in described olivine matrix surface and coat the carbon film that a layer thickness is 2～100nm, the content of carbon accounts for 1～20wt% of olivine matrix weight.On described coating one deck carbon film olivine matrix, the direct growth carbon nano-tube is or/and the olivine carbon bobbles composite material that nanofiber obtains again, and described carbon nano-tube or nanofiber diameter are 1～200nm, and length is 50nm～100um.
The average grain diameter of described olivine matrix is 50nm～50um, preferred 50～500nm, and its pattern both can be irregular, also can be for rule, preferred geometric shape be a sphere.
Described olivine matrix promptly has the basis material of olivine structural, and it is the LiMPO of pure phase or doping
4, its chemical composition can be represented with following formula:
Li
xA
aM
mB
bPO
zN
n
Wherein, A is Na, Mg, Ti, V, Cr, Cu, Mn, Co, Ni, Zn, Ga, In, Ge, Ag, Hg, Au, Zr, Nb, or W;
M is Fe, Co, Mn, Ni, or V;
B is Li, Na, K, Ca, Mg, Ti, V, Cr, Cu, Mn, Co, Ni, Zn, Ga, In, Ge, Ag, Hg, Au, Zr, Nb, or W;
And M and B are not with a kind of element simultaneously;
X, a, m, b, z, n represents molar percentage, 0.9≤x≤1.8; 0≤a≤0.1; 0.5≤m≤1; 0≤b≤0.5; 3≤z≤4; 0≤n≤1;
Preferred olivine matrix is LiFePO
4
Described carbon nano-tube or nanofiber diameter are 1～200nm, and length is 50nm～100um, and preferred diameter is 10～100nm, length is 200nm～20um, it both can have straight geometry appearance, also can have the geometry appearance of bending or spiral, both vertical matrix LiMPO
4The particle surface oriented growth also can the non-directional growth.
Olivine carbon bobbles composite material provided by the invention also is included in described olivine matrix surface and coats the carbon film that a layer thickness is 2～100nm, the content of carbon accounts for 1～20wt% of olivine matrix weight, the thickness of preferred carbon coating layer is 2～20nm, and the content of carbon accounts for 1～5wt% of olivine matrix weight.
Olivine carbon bobbles composite material provided by the invention is to prepare by following method, specifically comprises the steps:
The preparation of step 1, olivine basis material.
Chemical composition is Li
xA
aM
mB
bPO
zN
nPure phase or the LiMPO of doping
4Preparation technology with reference to United States Patent (USP) 5,910,382 and 6,514,640, disclosed method among the Chinese patent 200410031151.x, 200410101618.3 and 200410003477.1, use conventional solid phase synthesis process, solvent thermal process, the LiMPO of preparation such as fuse salt growth method pure phase
4, use conventional solid phase synthesis process, the LiMPO that preparation such as liquid phase coprecipitation is mixed
4
Preparation technology's list of references 1:J.Electrochem.Soc.149 (9) of the olivine matrix of coated with carbon, A1184-A1189 (2002) is at the LiMPO for preparing pure phase or doping
4After, by conventional chemical vapour deposition (CVD), methods such as solid-phase sintering coat carbon-coating, also can be at solid phase synthesis LiFePO on its surface
4Process in, add carbon matrix precursor, form carbon coating layer during again by solid-phase sintering.
Consider that from cost and technology controlling and process the present invention prepares all preferred solid phase synthesis process of above-mentioned three kinds of olivine basis materials, but is not limited to this.
Step 2, on the olivine basis material carbon nano-tube or/and nanofiber.
The present invention preferably use the slaine infusion process on the olivine basis material carbon nano-tube or/and nanofiber,
Specifically comprise the steps:
1) preparation is used for carbon nano-tube or/and the catalyst solution of nanofiber.
With the Fe (NO that is selected from as catalyst
3)
39H
2O, FeSO
47H
2O, FeCl
36H
2O, Co (NO
3)
26H
2O, Co (CH
3COO)
24H
2O, Ni (NO
3)
26H
2O, (NH
4)
6Mo
7O
244H
2O, and Cu (NO
3)
26H
2One or more salt among the O add in distilled water, ethanol, methyl alcohol, isopropyl alcohol, ethylene glycol or the glycerol solution one or more, are mixed with the catalyst solution of 0.0001～0.1M.
2) with olivine substrate material surface supported catalyst particles.
The olivine basis material for preparing in the step 1 is added step 2 1) in catalyst solution in, the weight ratio of catalyst in the catalyst solution and olivine matrix is 1: 1～1000, ℃ abundant the stirring 5 minutes～48 hours in room temperature～200, left standstill then 5～72 hours, Separation of Solid and Liquid, isolated solid obtains the olivine basis material of catalyst supported on surface particle 20～200 ℃ of dryings 30 minutes～48 hours.
3) at olivine substrate material surface carbon nano-tube or/and nanofiber.
With step 2 2) in the olivine basis material of the catalyst supported on surface particle that obtains place a heatproof container (as graphite boat, aluminium oxide boat, the iron boat, or stainless steel boat), the tube furnace that the air-tightness of packing into then is good, box type furnace or rotary drum furnace, feed the gaseous mixture of argon gas or argon gas and hydrogen, temperature programming to 450 then～900 ℃ will be reduced to metal as the slaine of catalyst precursor; After being raised to target temperature, furnace gas is converted to carbon-source gas (acetylene, ethene, methane, carbon monoxide, toluene or other carbon-source gas) or is converted to the gaseous mixture of argon gas, nitrogen or hydrogen and above-mentioned carbon-source gas, after constant temperature carried out chemical vapour deposition (CVD) in 20 minutes～48 hours, naturally cool to room temperature, the product that obtains is olivine carbon bobbles composite material of the present invention.
Can be in step 2) in add the load capacity that surfactant comes control catalyst, particle size;
Can be in step 2) in add chemical reducing agent, in liquid phase, directly metallic reducing is deposited on the olivine basis material.
According to existing literature report, the method that load is used for the catalyst granules of carbon nano-tube and nanofiber on other class basis material comprises that also the physical mechanical ball milling mixes several different methods such as vapour deposition.The present invention also can adopt these methods metal supported catalyst on the olivine basis material.But from preparation cost, the complexity of technology controlling and process and technology is considered, preferable alloy salt dipping method of the present invention, but be not limited to this.
Olivine carbon bobbles composite material provided by the invention both can directly use in serondary lithium battery as positive electrode active materials, also can be used as additive, with existing LiCoO
2, LiMn
2O
4, LiNiCoMnO
2Mix use Deng positive electrode, its content accounts for 5～98wt% of the total weight of positive electrode.
Olivine carbon bobbles composite material provided by the invention can improve the multiplying power and the security performance of existing positive electrode and battery.It is big that the serondary lithium battery that contains this olivine carbon bobbles composite material has power density, remarkable advantages such as fail safe height.This class serondary lithium battery is applicable to that various mobile electronic devices maybe need the equipment of mobile driven by energy, mobile phone for example, notebook computer, portable video recorder, electronic toy, high power electrokinetic cell particularly, as be used in electric tool, electric automobile, hybrid vehicle, electric topedo, fields such as accumulation power supply, and be not limited to this.
The advantage of olivine carbon bobbles composite material provided by the invention is:
1) the present invention has prepared the LiMPO with the pure phase with olivine structural first
4, the LiMPO that mixes
4Or the LiMPO of coated with carbon
4Be matrix, the olivine carbon bobbles composite material of the carbon nano-tube of having grown on it or nanofiber.
2) because in this olivine carbon bobbles composite material provided by the invention, carbon nano-tube or nanofiber are the LiMPO that is grown directly upon dispersion
4On the particle, avoided adopting the uneven shortcoming of dispersion that carbon nano-tube or nanofiber were caused by time in the physical mixed in active material.In addition, because the carbon nano-tube or the nanofiber of conduction are grown directly upon the active particle surface, its length generally surpasses inner LiMPO as basis material
4The diameter of particle; like this when the particle of these composite materials contacts; carbon nano-tube or carbon fiber that can be by particle surface overlap mutually with adjacent particle and to form continuous uniform conductive network, therefore can keep good electrical contact by a direct sum active material.
3) according to the transport theory of solid state ionics about ion and electronics, transporting of ion and electronics is to be mutually related.Electron transport fast will help transporting of ion, otherwise slower electron transport will slow down transporting of ion.The particle surface of olivine carbon bobbles composite material provided by the invention is carbon nano-tube or carbon fiber, when this material uses as positive electrode active materials in containing the serondary lithium battery of liquid electrolyte, in nanotube surface, because strong adsorption capacity, electrolyte solution forms thin electrolyte adsorption layer in carbon nano tube surface, in charge and discharge process, under effect of electric field, electronics will transport along carbon nano-tube or electric conduction of carbon fiber network high-speed, this will play pulling function to the ion transport on surface, strengthened surperficial ionic conduction, thereby help the transmission of lithium ion in electrode material surface, promptly be particularly conducive to the high-speed transfer of ion on the electrode active material surface, the fast charging and discharging performance of material is just superior especially like this, so this material is highly suitable in the high power serondary lithium battery and directly uses as positive electrode.
4) composite material provided by the invention, because the inner base material is the active material of storage lithium, the outside can be connected to form the favorable conductive network.Mix use with it or as conductive additive with other positive electrode, can improve the multiplying power of existing positive electrode and battery when being used for serondary lithium battery, have the big remarkable advantage that waits of power density.In addition, since the material of olivine structural, LiFePO when special
4The material of class has good fail safe, can also improve the security performance of other positive electrode.
Embodiment
Embodiment 1, pure phase LiFePO4 carbon bobbles composite material 1
Pure phase LiFePO
4Can be by following steps by the solid phase synthesis process preparation of two steps.At first, take by weighing LiF, FeC according to mol ratio
2O
42H
2O and NH
4H
2PO
4(mol ratio is 1: 1: 1), after the mechanical mixture (ball milling, rotating speed are 500 rev/mins, 3 hours), with this mixture at high-purity Ar gas/H
2Gas gaseous mixture (H
2The gas volume ratio accounts for 8%) (heat treated step is: be warming up to 400 ℃ with 1 hour from room temperature to protect heat treatment down; at 400 ℃ of constant temperature after 4 hours; with dropping to room temperature in two hours); (rotating speed is 500 rev/mins to ball milling once more; 1 hour) after; mixture once more sintering (sintering step is: be warming up to 600 ℃ with 2 hours from room temperature, at 600 ℃ of constant temperature after 8 hours, with dropping to room temperature in 3 hours.Obtain pure phase LiFePO
4Dusty material, average grain diameter are 200nm.
Being prepared as of catalyst solution: take by weighing 0.01mol Ni (NO
3)
26H
2O puts into beaker, adds 100ml ethylene glycol, and stirring and dissolving obtains 0.1M Ni (NO
3)
26H
2In the ethylene glycol solution of O.The method of load is: with the LiFePO of the above-mentioned preparation of 2g
4Powder joins the 0.1M Ni (NO of 100ml
3)
26H
2In the O ethylene glycol solution, stirred 10 hours at 60 ℃, by Buchner funnel or other filter plant with Separation of Solid and Liquid, then 80 ℃ of following vacuumizes 10 hours.The method of carbon nano-tube is: the gained material is placed in the aluminium oxide boat, the tube furnace of packing into then charges into argon gas, and flow is 80sccm, after the temperature programming to 600 ℃, gas is converted to the gaseous mixture of acetylene and hydrogen, and its ratio is 3: 2 (v/v), and total flow is 100sccm, after constant temperature carried out chemical vapour deposition (CVD) in 2 hours, gas is converted to argon gas, naturally cools to room temperature, products therefrom is LiFePO
4Carbon bobbles composite material 1, wherein the average diameter of carbon nano-tube is 20nm, length is 100 μ m.
Use: with the LiFePO that obtains
4Carbon bobbles composite material 1 mixes formation slurry (active material: acetylene black: PVDF=90: 5: 5) at normal temperatures and pressures with the n-formyl sarcolysine base pyrrolidone solution of acetylene black and 10% Kynoar (PVDF), evenly be coated on the aluminum substrates, then 100 ℃ of vacuumizes after 5 hours, the film of gained is compressed under 10MPa pressure, the about 100 μ m of the film thickness of gained are cut into the positive pole of the electrode slice of 1x1cm as simulated battery.
The negative pole of simulated battery uses the lithium sheet, and electrolyte is 1mol LiPF
6Be dissolved in the mixed solvent of 1L EC and DMC (volume ratio 1: 1).With positive pole, negative pole, electrolyte, barrier film is assembled into simulated battery in the glove box of argon shield.
The electro-chemical test step of simulated battery: at first charge to 4.2V with 30mA/g, the multiplying power current discharge is to 2.0V then, and the capacity of being emitted is with LiFePO
4The Mass Calculation of carbon bobbles composite material reaches 120mAh/g, when discharging current increases to 1500mA/g, the discharge capacity of this material is 80mAh/g, this current density, the charge-discharge magnification that is equivalent to 10C, when further raising current density during to 6000mA/g, the discharge capacity of this material is 60mAh/g.This result shows LiFePO
4Carbon bobbles composite material 1 has high-multiplying power discharge characteristic preferably.
Embodiment 2, doped iron lithium phosphate carbon bobbles composite material 2
Doped iron lithium phosphate Li
0.99Na
0.01FePO
4Can prepare (with reference to Chinese patent 200410031151.x) by following steps.At first, take by weighing Li according to mol ratio
2CO
3, Na
2CO
3, FeC
2O
42H
2O and NH
4H
2PO
4, behind the mechanical ball milling (rotating speed is 500 rev/mins, 3 hours), with this mixture at Ar-H
2Gaseous mixture (Ar: H
2=92: 8; v/v) (heat treated step is: be warming up to 500 ℃ with 1 hour from room temperature to protect heat treatment down; at 500 ℃ of constant temperature after 8 hours; with dropping to room temperature in two hours); once more behind the ball milling (rotating speed is 500 rev/mins, 1 hour), mixture once more sintering (sintering step is: be warming up to 700 ℃ with 2 hours from room temperature; at 700 ℃ of constant temperature after 24 hours, with dropping to room temperature in 3 hours).Obtain doped iron lithium phosphate Li
0.99Na
0.01FePO
4Dusty material, average grain diameter are 500nm.
Take by weighing 0.001mol Co (NO
3)
26H
2O puts into beaker, adds 100ml ethanol, stirring and dissolving; Then with 10g Li
0.99Na
0.01FePO
4Join in this solution, stirred 10 hours at 25 ℃, by Buchner funnel or other filter plant with Separation of Solid and Liquid, then 80 ℃ of following vacuumizes 10 hours; The gained material is placed in the aluminium oxide boat, the tube furnace of packing into then charges into argon gas, and flow is 80sccm, after the temperature programming to 800 ℃, gas is converted to the gaseous mixture of ethene and hydrogen, and its ratio is 4: 1 (v/v), and total flow is 100sccm, after constant temperature carried out chemical vapour deposition (CVD) in 2 hours, gas is converted to argon gas, naturally cools to room temperature, products therefrom is LiFePO
4Carbon bobbles composite material 2, wherein the average diameter of carbon nano-tube is 5nm, length is 10um.
The doped iron lithium phosphate carbon bobbles composite material 2 that obtains is mixed formation slurry (active material: PVDF=98: 2) at normal temperatures and pressures with the n-formyl sarcolysine base pyrrolidone solution of 10% Kynoar (PVDF), evenly be coated on the aluminum substrates, then 100 ℃ of vacuumizes after 5 hours, the film of gained is compressed under 10MPa pressure, the about 60 μ m of the film thickness of gained are cut into the positive pole of the electrode slice of 1x1cm as simulated battery.
The negative pole of simulated battery uses the lithium sheet, and electrolyte is 1mol LiPF
6Be dissolved in the mixed solvent of 1L EC and DMC (volume ratio 1: 1).With positive pole, negative pole, electrolyte, barrier film is assembled into simulated battery in the glove box of argon shield.
The electro-chemical test step of simulated battery: at first charge to 4.2V with 30mA/g, the multiplying power current discharge is to 2.0V then, the capacity of being emitted reaches 130mAh/g with doped iron lithium phosphate carbon bobbles composite material 2 Mass Calculation, when discharging current increases to 1500mA/g, the discharge capacity of this material is 110mAh/g, and this current density is equivalent to the charge-discharge magnification of 10C, when further raising current density during to 6000mA/g, the discharge capacity of this material is 80mAh/g.This result shows that doped iron lithium phosphate carbon bobbles composite material 2 has high-multiplying power discharge characteristic preferably.
Embodiment 3, doped iron lithium phosphate carbon bobbles composite material 3
Doped iron lithium phosphate LiFe
0.99Na
0.01PO
4Can prepare (with reference to Chinese patent 200410031151.x) by following steps.At first, take by weighing Li according to mol ratio
2CO
3, Na
2CO
3, FeC
2O
42H
2O and NH
4H
2PO
4, behind the mechanical ball milling (rotating speed is 500 rev/mins, 3 hours), with this mixture at Ar-H
2Gaseous mixture (Ar: H
2=92: 8; v/v) (heat treated step is: be warming up to 450 ℃ with 1 hour from room temperature to protect heat treatment down; at 450 ℃ of constant temperature after 8 hours; with dropping to room temperature in 5 hours); once more behind the ball milling (rotating speed is 500 rev/mins, 1 hour), mixture once more sintering (sintering step is: be warming up to 800 ℃ with 2 hours from room temperature; at 800 ℃ of constant temperature after 24 hours, with dropping to room temperature in 3 hours).Obtain doped iron lithium phosphate LiFe
0.99Na
0.01PO
4Dusty material, average grain diameter are 300nm.
Take by weighing 0.0001mol Fe (NO
3)
26H
2O puts into beaker, adds the 100ml isopropyl alcohol, stirring and dissolving; Then with 10g LiFe
0.99Na
0.01PO
4Powder (average grain diameter is 200nm) joins in this solution, stirred 1 hour at 25 ℃, by Buchner funnel or other filter plant with Separation of Solid and Liquid, then 100 ℃ of following vacuumizes 10 hours; The gained material is placed in the aluminium oxide boat, the tube furnace of packing into then, charge into argon gas, flow is 80sccm, after the temperature programming to 600 ℃, gas is converted to acetylene gas, total flow is 100sccm, and constant temperature was converted to argon gas with gas after carrying out chemical vapour deposition (CVD) in 2 hours, naturally cool to room temperature, products therefrom is LiFePO
4Carbon bobbles composite material, wherein the average diameter of carbon nano-tube is 50nm, length is 0um.
Embodiment 4, doped iron lithium phosphate carbon bobbles composite material 4
Nitrogen doped iron phosphate lithium anode material Li
1.8Co
0.1FePO
3N can prepare by following steps.At first, with Li
3N mixes the back in high-purity N with the Co powder
2Made Li in 12 hours 700 ℃ of heating down
2.4Co
0.3N.Take by weighing LiPO then
3, Li
2.4Co
0.3N, Fe
3N
2(mol ratio is 3: 1: 1) filling high-purity N
2In the sealing ball grinder of gas behind the mechanical ball milling (rotating speed is 500 rev/mins, 3 hours), with this mixture in high-purity N
2Sample is taken out in heat treatment under the gas shiled (heat treated step is: be warming up to 600 ℃ with 3 hours from room temperature, at 600 ℃ of constant temperature after 8 hours, with dropping to room temperature in two hours).Obtain doped iron lithium phosphate Li
1.8Co
0.1FePO
3N dusty material, average grain diameter are 1um.
Take by weighing 0.0001mol (NH
4)
6Mo
7O
244H
2O puts into beaker, adds 100ml methyl alcohol, stirring and dissolving; Then with 10g Li
1.8Co
0.1FePO
3N powder (average grain diameter is 500nm) joins in this solution, stirred 10 hours at 25 ℃, by Buchner funnel or other filter plant with Separation of Solid and Liquid, then 100 ℃ of following vacuumizes 10 hours; The gained material is placed in the aluminium oxide boat, the tube furnace of packing into then, charge into argon gas, flow is 80sccm, after the temperature programming to 800 ℃, gas is converted to argon gas stream crosses the toluene bottle, flow is 100sccm, and constant temperature was converted to argon gas with gas after carrying out chemical vapour deposition (CVD) in 20 hours, naturally cool to room temperature, products therefrom is LiFePO
4Carbon bobbles composite material, average diameter of carbon fiber is 100nm on it, length is 50um.
The LiFePO4 carbon bobbles composite material of embodiment 5, oxygen-containing vacancy
The LiFePO4 matrix material LiFePO of oxygen-containing vacancy
3.998Can prepare by following steps.At first, take by weighing LiF, FeC at 1: 1: 1 according to mol ratio
2O
42H
2O and NH
4H
2PO
4, behind the mechanical ball milling (rotating speed is 500 rev/mins, 3 hours), with this mixture at high-purity Ar gas/H
2Gas gaseous mixture (H
2The gas volume ratio accounts for 8%) (heat treated step is: be warming up to 400 ℃ with 1 hour from room temperature to protect heat treatment down; at 400 ℃ of constant temperature after 4 hours; with dropping to room temperature in two hours); (rotating speed is 500 rev/mins to ball milling once more; 1 hour) after; mixture once more sintering (sintering step is: be warming up to 600 ℃ with 2 hours from room temperature, at 600 ℃ of constant temperature after 8 hours, with dropping to room temperature in 3 hours.Obtain the LiFePO4 matrix material LiFePO of oxygen-containing vacancy
3.998Dusty material, average grain diameter are 100nm.
Take by weighing 0.001mol Ni (NO
3)
26H
2O and 0.000015mol Cu (NO
3)
26H
2O adds the 100ml isopropyl alcohol, stirring and dissolving in beaker.Then with 10g LiFePO
3.998Powder joins in this solution, stirred 5 hours at 25 ℃, by Buchner funnel or other filter plant with Separation of Solid and Liquid, then 100 ℃ of following vacuumizes 10 hours; The gained material is placed in the aluminium oxide boat, the tube furnace of packing into then, charge into argon gas, flow is 80sccm, after the temperature programming to 800 ℃, gas is converted to methane gas, total flow is 100sccm, and constant temperature was converted to argon gas with gas after carrying out chemical vapour deposition (CVD) in 20 hours, naturally cool to room temperature, products therefrom is LiFePO
4Carbon bobbles composite material, average diameter of carbon fiber is 100nm on it, length is 10um.
Embodiment 6～51, olivine carbon bobbles composite material 6～51
Similar with embodiment 2～5, different is to have prepared the Li doped MPO that contains different doped chemicals and ratio
4, basis material, and the LiMPO of oxygen-containing vacancy
4Basis material, its expression formula can be written as Li
xA
aM
mB
bPO
zN
nWherein, A is Na, Mg, Ti, V, Cr, Cu, Mn, Co, Ni, Zn, Ga, In, Ge, Ag, Hg, Au, Zr, Nb, W; M is Fe, Co, Mn, Ni, V; B is Li, Na, K, Ca, Mg, Ti, V, Cr, Cu, Mn, Co, Ni, Zn, Ga, In, Ge, Ag, Hg, Au, Zr, Nb, W; And M and B are not a kind of element simultaneously; X, a, m, b, z, n represents molar percentage, 0.9≤x≤1.8; 0≤a≤0.1; 0.5≤m≤1; 0≤b≤0.5; 3≤z≤4; 0≤n≤1.
The preparation method of above-mentioned basis material is similar to embodiment 2～5, different is the raw material difference that adopts, the doped chemical difference of adding, about the preparation of these materials, can be with reference to (Wang Deyu, Chen Liquan, Li Hong, yellow-study outstanding person, a kind of positive electrode and purposes that is used for serondary lithium battery, 200410031151.x; Li Hong, yellow-study outstanding person is used for the lithium iron phosphate positive material and uses thereof of the oxygen-containing vacancy of serondary lithium battery, 200410101618.3; Li Hong, yellow-study outstanding person, Wang Deyu, Chen Liquan, positive electrode of a kind of nitrogen phosphate that is used for serondary lithium battery and uses thereof, 200410037502.8).The chemical composition of basis material 6～51 is referring to subordinate list 1.
On above-mentioned different basis material, the method and the embodiment 1～5 of growth carbon nano-fiber and carbon nano-tube are similar, different is the catalyst system therefor kind, content, the carbon-source gas kind, synthesis temperature, the time there are differences, these differences cause the carbon nano-tube that grows out or nanofiber at diameter, there are differences on the length.The feature of these olivine carbon bobbles composite materials is listed in table 1.
Embodiment 52, carbon coat olivine carbon bobbles composite material 52
Carbon coats olivine LiMPO
4Can prepare by following steps.At first, take by weighing Li according to mol ratio
2CO
3, FeC
2O
42H
2O and NH
4H
2PO
4, behind the mechanical ball milling (rotating speed is 500 rev/mins, 3 hours), with this mixture at Ar-H
2Gaseous mixture (Ar: H
2=92: 8; v/v) (heat treated step is: be warming up to 400 ℃ with 1 hour from room temperature to protect heat treatment down; at 400 ℃ of constant temperature after 8 hours; with dropping to room temperature in two hours); add the carbon black of 10% weight ratio then; the water soluble starch of 10% weight ratio; and the ethanol of 20ml (volume of a container is 100ml) once more ball milling (rotating speed is 500 rev/mins; 1 hour) after; mixture once more sintering (sintering step is: be warming up to 600 ℃ with 2 hours from room temperature; at 600 ℃ of constant temperature after 24 hours, with dropping to room temperature in 3 hours).The basis material that obtains is the LiFePO of coated with carbon particle
4, LiFePO wherein
4Average grain diameter is 100nm, and the mass percent of carbon is 12% in the product, and the mass percent of LiFePO4 is 88%, and the thickness of carbon-coating is 20-30nm.
With the basis material that obtains, adopt similar and method embodiment 1～51, catalyst in the load, according to the condition of table 1, the carbon that obtains superficial growth carbon nano-tube or nanofiber coats olivine carbon bobbles composite material 52.The diameter of epontic carbon nano-tube is 50nm, and length is about 20um.
Embodiment 53～57, carbon coat olivine carbon bobbles composite material 53～57
Be similar to embodiment 52, obtain carbon and coat olivine LiMPO
4The olivine LiMPO that different coated
4The material difference, its preparation method is identical with embodiment 6～51.Carbon coats the final content difference of back carbon in basis material, not being both because due to the part by weight difference of carbon black that adds and water soluble starch of content.The amount of carbon black is adding fashionable 0～20% weight ratio that generally is controlled at, and the carbon residue rate of water soluble starch generally about 25%, generally is controlled at about 0～40% during interpolation.Water soluble starch and carbon black can not add when synthetic carbon coats the olivine material simultaneously, but must add one of them.Final carbon is no more than 20% in the mass percent that carbon coats in the olivine basis material, is not less than 1%.All these test difference, referring to table 2.
With the basis material that obtains, adopt similar and method embodiment 1～52, catalyst in the load is then by chemical vapor deposition growth carbon nano-tube or carbon fiber.It is irrelevant that the diameter of carbon nano-tube and carbon fiber and length and carbon coat the olivine basis material, only relevant with the load and the growth conditions of catalyst, and the carbon that finally obtains coats the principal character of olivine carbon bobbles composite material and lists in table 2.
Embodiment 58, olivine carbon bobbles composite material are as the purposes 1 of anode of secondary lithium battery additive
With the pure phase LiFePO4 carbon bobbles composite material of embodiment 1 preparation, with cobalt acid lithium (LiCoO
2, commercial product, diameter are 20 microns, bulk density is 3g/cm
3) and the n-formyl sarcolysine base pyrrolidone solution of 10% Kynoar (PVDF) mix at normal temperatures and pressures and form slurry (pure phase LiFePO4 carbon bobbles composite material 1: LiCoO wherein
2: PVDF=10: 85: 5), evenly be coated on the aluminum substrates, then 100 ℃ of vacuumizes after 5 hours, the film of gained compressed under 10MPa pressure, the about 100 μ m of the film thickness of gained are cut into the positive pole of the electrode slice of 1x1cm as simulated battery.
The negative pole of simulated battery uses the lithium sheet, and electrolyte is 1mol LiPF
6Be dissolved in the mixed solvent of 1L EC and DMC (volume ratio 1: 1).With positive pole, negative pole, electrolyte, barrier film is assembled into simulated battery in the glove box of argon shield.
The electro-chemical test step of simulated battery: at first charge to 4.2V with 30mA/g, the multiplying power current discharge is to 2.0V then, and the capacity of being emitted is with LiFePO
4The Mass Calculation that carbon bobbles composite material adds cobalt acid lithium reaches 130mAh/g, when discharging current increases to 1500mA/g, the discharge capacity of this material is 90mAh/g, this current density, the charge-discharge magnification that is equivalent to 10C, when further raising current density during to 6000mA/g, the discharge capacity of this material is 60mAh/g, this current density is equivalent to the charge-discharge magnification of 40C. and this result shows LiFePO
4Carbon bobbles composite material 1 has significantly improved the high-multiplying power discharge characteristic of cobalt acid lithium as functional additive.
Embodiment 59, olivine carbon bobbles composite material are as the purposes 2 of anode of secondary lithium battery additive
With the doped iron lithium phosphate carbon bobbles composite material 2 of embodiment 2 preparations, with LiMn2O4 (LiMn
2O
4, commercial product, diameter are 15 microns, bulk density is 2.8g/cm
3) and the n-formyl sarcolysine base pyrrolidone solution of 10% Kynoar (PVDF) mix at normal temperatures and pressures and form slurry (wherein the doped iron lithium phosphate carbon bobbles composite material 2: LiMn
2O
4: PVDF=20: 75: 5), evenly be coated on the aluminum substrates, then 100 ℃ of vacuumizes after 5 hours, the film of gained compressed under 10MPa pressure, the about 100 μ m of the film thickness of gained are cut into the positive pole of the electrode slice of 1x1cm as simulated battery.
The negative pole of simulated battery uses the lithium sheet, and electrolyte is 1mol LiPF
6Be dissolved in the mixed solvent of 1L EC and DMC (volume ratio 1: 1).With positive pole, negative pole, electrolyte, barrier film is assembled into simulated battery in the glove box of argon shield.
The electro-chemical test step of simulated battery: at first charge to 4.2V with 30mA/g, the multiplying power current discharge is to 2.0V then, and the capacity of being emitted is with LiFePO
4The Mass Calculation that carbon bobbles composite material adds LiMn2O4 reaches 110mAh/g, when discharging current increases to 1500mA/g, the discharge capacity of this material is 80mAh/g, this current density, the charge-discharge magnification that is equivalent to 10C, when further raising current density during to 6000mA/g, the discharge capacity of this material is 70mAh/g, this current density is equivalent to the charge-discharge magnification of 40C. and this result shows that doped iron lithium phosphate carbon bobbles composite material 2 has significantly improved the high-multiplying power discharge characteristic of LiMn2O4 as functional additive.
Embodiment 60, olivine carbon bobbles composite material are as the purposes 3 of anode of secondary lithium battery additive
According to embodiment 59, with the doped iron lithium phosphate carbon bobbles composite material 2 and lithium nickel cobalt manganese oxygen (LiNi of embodiment 2 preparations
0.4Co
0.2Mn
0.4O
2, commercial product, diameter are 5 microns, bulk density is 2.4g/cm
3) and the n-formyl sarcolysine base pyrrolidone solution of 10% Kynoar (PVDF) mix at normal temperatures and pressures and form slurry (wherein the doped iron lithium phosphate carbon bobbles composite material 2: LiNi
0.4Co
0.02Mn
0.4O
2: PVDF=30: 60: 5), evenly be coated on the aluminum substrates, then 100 ℃ of vacuumizes after 5 hours, the film of gained compressed under 10MPa pressure, the about 100 μ m of the film thickness of gained are cut into the positive pole of the electrode slice of 1x1cm as simulated battery.
The negative pole of simulated battery uses the lithium sheet, and electrolyte is 1mol LiPF
6Be dissolved in the mixed solvent of 1L EC and DMC (volume ratio 1: 1).With positive pole, negative pole, electrolyte, barrier film is assembled into simulated battery in the glove box of argon shield.
The electro-chemical test step of simulated battery: at first charge to 4.2V with 30mA/g, the multiplying power current discharge is to 2.0V then, and the capacity of being emitted is with LiFePO
4The Mass Calculation that carbon bobbles composite material adds lithium nickel cobalt manganese oxygen reaches 130mAh/g, when discharging current increases to 1500mA/g, the discharge capacity of this material is 100mAh/g, this current density, the charge-discharge magnification that is equivalent to 10C, when further raising current density during to 6000mA/g, the discharge capacity of this material is 90mAh/g, this current density is equivalent to the charge-discharge magnification of 40C.This result shows that doped iron lithium phosphate carbon bobbles composite material 2 has significantly improved the high-multiplying power discharge characteristic of lithium nickel cobalt manganese oxygen as functional additive.
Embodiment 61, olivine carbon bobbles composite material are as the purposes 4 of anode of secondary lithium battery additive
According to embodiment 59, with the doped iron lithium phosphate carbon bobbles composite material 2 and lithium nickel cobalt manganese oxygen (LiNi of embodiment 2 preparations
0.33Co
0.33Mn
0.33O
2, commercial product, diameter are 8 microns, bulk density is 2.6g/cm
3) and the n-formyl sarcolysine base pyrrolidone solution of 10% Kynoar (PVDF) mix at normal temperatures and pressures and form slurry (wherein the doped iron lithium phosphate carbon bobbles composite material 2: LiNi
0.4Co
0.2Mn
0.4O
2: PVDF=5: 90: 5), evenly be coated on the aluminum substrates, then 100 ℃ of vacuumizes after 5 hours, the film of gained compressed under 10MPa pressure, the about 100 μ m of the film thickness of gained are cut into the positive pole of the electrode slice of 1x1cm as simulated battery.
The negative pole of simulated battery uses the lithium sheet, and electrolyte is 1mol LiPF
6Be dissolved in the mixed solvent of 1L EC and DMC (volume ratio 1: 1).With positive pole, negative pole, electrolyte, barrier film is assembled into simulated battery in the glove box of argon shield.
The electro-chemical test step of simulated battery: at first charge to 4.2V with 30mA/g, the multiplying power current discharge is to 2.0V then, and the capacity of being emitted is with LiFePO
4The Mass Calculation that carbon bobbles composite material adds lithium nickel cobalt manganese oxygen reaches 150mAh/g, when discharging current increases to 1500mA/g, the discharge capacity of this material is 120mAh/g, this current density, the charge-discharge magnification that is equivalent to 10C, when further raising current density during to 6000mA/g, the discharge capacity of this material is 100mAh/g, this current density is equivalent to the charge-discharge magnification of 40C.This result shows that doped iron lithium phosphate carbon bobbles composite material 2 has significantly improved the high-multiplying power discharge characteristic of lithium nickel cobalt manganese oxygen as functional additive.
Embodiment 62, olivine carbon bobbles composite material are as the purposes 5 of active material of anode of secondary lithium battery
According to embodiment 59, with the doped iron lithium phosphate carbon bobbles composite material 2 and Li-Ni-Mn-O (LiNi of embodiment 2 preparations
0.8Mn
0.2O
2, commercial product, diameter are 10 microns, bulk density is 2.9g/cm
3) and the n-formyl sarcolysine base pyrrolidone solution of 10% Kynoar (PVDF) mix at normal temperatures and pressures and form slurry (wherein the doped iron lithium phosphate carbon bobbles composite material 2: LiNi
0.8Mn
0.O
2: PVDF=90: 5: 5), evenly be coated on the aluminum substrates, then 100 ℃ of vacuumizes after 5 hours, the film of gained compressed under 10MPa pressure, the about 100 μ m of the film thickness of gained are cut into the positive pole of the electrode slice of 1x1cm as simulated battery.
The negative pole of simulated battery uses the lithium sheet, and electrolyte is 1mol LiPF
6Be dissolved in the mixed solvent of 1L EC and DMC (volume ratio 1: 1).With positive pole, negative pole, electrolyte, barrier film is assembled into simulated battery in the glove box of argon shield.
The electro-chemical test step of simulated battery: at first charge to 4.2V with 30mA/g, the multiplying power current discharge is to 2.0V then, and the capacity of being emitted is with LiFePO
4The Mass Calculation that carbon bobbles composite material adds Li-Ni-Mn-O reaches 150mAh/g, when discharging current increases to 1500mA/g, the discharge capacity of this material is 110mAh/g, this current density, the charge-discharge magnification that is equivalent to 10C, when further raising current density during to 6000mA/g, the discharge capacity of this material is 95mAh/g, this current density is equivalent to the charge-discharge magnification of 40C.This result shows that the anode composite that doped iron lithium phosphate carbon bobbles composite material 2 and Li-Ni-Mn-O are formed has shown good high-multiplying power discharge characteristic.
The principal character of table 1, olivine carbon bobbles composite material provided by the invention
Table 2, carbon provided by the invention coat the feature of olivine carbon bobbles composite material
Claims (8)
1. an olivine carbon bobbles composite material comprises an olivine matrix; It is characterized in that: direct growth has carbon nano-tube or/and nanofiber on described olivine matrix, and described carbon nano-tube or nanofiber diameter are 1～200nm, and length is 50nm～100um.
2. olivine carbon bobbles composite material as claimed in claim 1, it is characterized in that: the olivine matrix in the described olivine carbon bobbles composite material, also be included in described olivine matrix surface and coat the carbon film that a layer thickness is 2～100nm, the content of carbon accounts for 1～20wt% of olivine matrix weight, on described coating one deck carbon film olivine matrix, the direct growth carbon nano-tube is or/and the olivine carbon bobbles composite material that nanofiber obtains again, described carbon nano-tube or nanofiber diameter are 1～200nm, and length is 50nm～100um.
3. olivine carbon bobbles composite material as claimed in claim 1 or 2 is characterized in that: the average grain diameter of described olivine matrix is 50nm～50um.
4. olivine carbon bobbles composite material as claimed in claim 1 or 2 is characterized in that: the average grain diameter of described olivine matrix is 50～500nm.
5. olivine carbon bobbles composite material as claimed in claim 1 or 2 is characterized in that: the chemical composition of described olivine matrix is represented with following formula:
Li
xA
aM
mB
bPO
zN
n
Wherein, A is Na, Mg, Ti, V, Cr, Cu, Mn, Co, Ni, Zn, Ga, In, Ge, Ag, Hg, Au, Zr, Nb, or W;
M is Fe, Co, Mn, Ni, or V;
B is Li, Na, K, Ca, Mg, Ti, V, Cr, Cu, Mn, Co, Ni, Zn, Ga, In, Ge, Ag, Hg, Au, Zr, Nb, or W;
And M and B are not with a kind of element simultaneously;
X, a, m, b, z, n represents molar percentage, 0.9≤x≤1.8; 0≤a≤0.1; 0.5≤m≤1; 0≤b≤0.5; 3≤z≤4; 0≤n≤1.
6. olivine carbon bobbles composite material as claimed in claim 1 or 2 is characterized in that: described carbon nano-tube or nanofiber diameter are 10～100nm, and length is 200nm～20um.
7. the described olivine carbon bobbles composite material of one of claim 1～6 is as the application of positive electrode active materials in serondary lithium battery.
8. the described olivine carbon bobbles composite material of one of claim 1～6 is mixed with existing positive electrode and use as the application of positive electrode active materials in serondary lithium battery, the content of described olivine carbon bobbles composite material accounts for 5～98wt% of the total weight of positive electrode.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100797645A CN100399608C (en) | 2005-06-28 | 2005-06-28 | Olivine carbon bobbles composite material and use thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100797645A CN100399608C (en) | 2005-06-28 | 2005-06-28 | Olivine carbon bobbles composite material and use thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1889290A CN1889290A (en) | 2007-01-03 |
| CN100399608C true CN100399608C (en) | 2008-07-02 |
Family
ID=37578553
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2005100797645A Active CN100399608C (en) | 2005-06-28 | 2005-06-28 | Olivine carbon bobbles composite material and use thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100399608C (en) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5118877B2 (en) | 2007-04-27 | 2013-01-16 | トヨタ自動車株式会社 | Secondary battery |
| US20120021291A1 (en) * | 2009-04-01 | 2012-01-26 | Shan Ji | Method for Producing a Carbon Composite Material |
| JP5623544B2 (en) * | 2009-12-04 | 2014-11-12 | ルート ジェイジェイ カンパニー リミテッド | Cathode active material precursor for lithium secondary battery containing nano hollow fiber type carbon, active material and method for producing the same |
| CN101834288A (en) * | 2010-03-23 | 2010-09-15 | 浙江大学 | Lithium iron phosphate/nano carbon composite material and preparation method thereof |
| CN101969112B (en) * | 2010-09-30 | 2013-05-08 | 湛江市聚鑫新能源有限公司 | Anode material and cathode material for lithium ion battery and modifying method thereof |
| CN102456881B (en) * | 2010-10-18 | 2014-03-12 | 中国科学院物理研究所 | Olivine type phosphate cathode material and preparation method thereof as well as positive electrode and battery both containing olivine type phosphate cathode material |
| CN102427130B (en) * | 2011-03-23 | 2013-11-06 | 上海中兴派能能源科技有限公司 | Lithium iron phosphate-carbon nanotube composite material, preparation method, and application thereof |
| CN103493265B (en) * | 2011-04-28 | 2016-10-12 | 昭和电工株式会社 | Anode materials for lithium secondary cells and manufacture method thereof |
| CN102956874B (en) * | 2011-08-17 | 2014-12-31 | 珠海银隆新能源有限公司 | Positive electrode film and lithium ion power battery, and preparation method thereof |
| CN102299308B (en) * | 2011-09-03 | 2014-05-07 | 深圳市贝特瑞新能源材料股份有限公司 | Lithium ion battery cathode material, and preparation method and lithium ion battery thereof |
| CN102867956A (en) * | 2012-09-24 | 2013-01-09 | 恒正科技（苏州）有限公司 | Preparation method of electro-chemical active material |
| CN103022495A (en) * | 2012-12-11 | 2013-04-03 | 彩虹集团公司 | Preparation method of high-electrical conductivity lithium iron phosphate |
| CN104638235A (en) * | 2015-01-16 | 2015-05-20 | 苏州容电储能科技有限公司 | Composite carbon nano tube array coated LiFePO4(lithium iron phosphate) electrode material and preparation method thereof |
| CN106129330B (en) * | 2016-08-29 | 2019-08-20 | 深圳市沃特玛电池有限公司 | A kind of positive plate of iron phosphate lithium battery and preparation method thereof, ferric phosphate lithium cell |
| CN109817907B (en) * | 2019-01-03 | 2021-02-26 | 北京泰丰先行新能源科技有限公司 | Positive electrode active material, positive electrode containing the same, and lithium secondary battery |
| CN111799459B (en) * | 2020-08-21 | 2021-09-17 | 中南大学 | Preparation method of sulfur composite cathode material and all-solid-state lithium sulfur battery |
| JP7460687B2 (en) | 2022-06-10 | 2024-04-02 | 株式会社日本製鋼所 | Functional base material manufacturing method |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1442917A (en) * | 2003-04-08 | 2003-09-17 | 复旦大学 | Carbon film and LiFePO4 composite nm conductive material and its synthesis method |
| WO2004001881A2 (en) * | 2002-06-21 | 2003-12-31 | Umicore | Carbon-coated li-containing powders and process for production thereof |
| JP2005123107A (en) * | 2003-10-20 | 2005-05-12 | Hitachi Maxell Ltd | Active material for electrochemical element, its manufacturing method, and the electrochemical element using the same |
-
2005
- 2005-06-28 CN CNB2005100797645A patent/CN100399608C/en active Active
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004001881A2 (en) * | 2002-06-21 | 2003-12-31 | Umicore | Carbon-coated li-containing powders and process for production thereof |
| CN1442917A (en) * | 2003-04-08 | 2003-09-17 | 复旦大学 | Carbon film and LiFePO4 composite nm conductive material and its synthesis method |
| JP2005123107A (en) * | 2003-10-20 | 2005-05-12 | Hitachi Maxell Ltd | Active material for electrochemical element, its manufacturing method, and the electrochemical element using the same |
Non-Patent Citations (1)
| Title |
|---|
| Various strategies to tune the ionic/electronic propertiersof electrode materials. J.M.Tarascon .etc.Dalton Trans. 2004 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1889290A (en) | 2007-01-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN100399608C (en) | Olivine carbon bobbles composite material and use thereof | |
| CN1328805C (en) | Negative electrode active material and use of secondary lithium battery | |
| CN101533904B (en) | Method for preparing lithium iron phosphate/nanometer carbon composite anode material | |
| Yao et al. | Novel carbon nanofiber-cobalt oxide composites for lithium storage with large capacity and high reversibility | |
| CN102468485B (en) | Lithium titanate composite material, preparation method thereof, and application thereof | |
| CN102456881B (en) | Olivine type phosphate cathode material and preparation method thereof as well as positive electrode and battery both containing olivine type phosphate cathode material | |
| CN100499223C (en) | Lamina-structure lithium-contained composite metal oxide coated with carbon and use thereof | |
| TW201212356A (en) | Negative electrode material for secondary battery with non-aqueous electrolyte, method for manufacturing negative electrode material for secondary battery with non-aqueous electrolyte, and lithium ion secondary battery | |
| CN101527353A (en) | Lithium ion battery anode composite material and manufacturing method thereof | |
| WO2011009231A1 (en) | Method for preparing carbon-coated positive material of lithium ion battery | |
| JP2018106974A (en) | Lithium ion secondary battery, method of producing electrode active material particle, and method of manufacturing lithium ion secondary battery | |
| Yuan et al. | Surfactant-assisted hydrothermal synthesis of V2O5 coated LiNi1/3Co1/3Mn1/3O2 with ideal electrochemical performance | |
| CN102522546A (en) | Method for preparing lithium iron phosphate serving as cathode material of nano-level lithium ion battery | |
| CN103384001B (en) | A kind of graphene combination electrode material and solid catalysis preparation method thereof | |
| Liu et al. | Carbonized polydopamine coated single-crystalline NiFe2O4 nanooctahedrons with enhanced electrochemical performance as anode materials in a lithium ion battery | |
| CN107611425B (en) | Fusiform zinc ferrite/carbon lithium ion battery nano composite negative electrode material and preparation method and application thereof | |
| Zhao et al. | Li4Ti5O12 epitaxial coating on LiNi0. 5Mn1. 5O4 surface for improving the electrochemical performance through solvothermal-assisted processing | |
| Wang et al. | ZnFe2O4-nanocrystal-assembled microcages as an anode material for high performance lithium-ion batteries | |
| Song et al. | Recent Progress in MOF‐Derived Porous Materials as Electrodes for High‐Performance Lithium‐Ion Batteries | |
| WO2002027822A1 (en) | Nanometer metal or nanometer alloy/carbon composite material, producing method thereof and the application thereof in a secondary lithium battery | |
| Wei et al. | Synthesis of a High-Capacity α-Fe2O3@ C Conversion Anode and a High-Voltage LiNi0. 5Mn1. 5O4 Spinel Cathode and Their Combination in a Li-Ion Battery | |
| Sen et al. | Nano dimensionality: a way towards better Li-ion storage | |
| Wang et al. | Micro/nanostructured MnCo2O4. 5 anodes with high reversible capacity and excellent rate capability for next generation lithium-ion batteries | |
| Wang et al. | Improving the stability properties of 5 V lithium nickel manganese oxide spinel by surface coating with cobalt aluminum oxides for lithium ion batteries | |
| JP2013258135A (en) | Silicon oxide particle, manufacturing method thereof, lithium ion secondary battery, and electrochemical capacitor |
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 | ||
| EE01 | Entry into force of recordation of patent licensing contract |
Assignee: Jiangsu Jing Yuan Li Energy Materials Co., Ltd. Assignor: Research Institute of Physics, Chinese Academy of Sciences Contract record no.: 2011320000531 Denomination of invention: Olivine carbon bobbles composite material and use thereof Granted publication date: 20080702 License type: Exclusive License Open date: 20070103 Record date: 20110406 |