CN101488584A - Asymmetric lithium iron phosphate cell using lithium titanate as main active substance of negative pole - Google Patents
Asymmetric lithium iron phosphate cell using lithium titanate as main active substance of negative pole Download PDFInfo
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Abstract
本发明公开了属于非水电解液的锂离子电池或混合电池技术领域的一种负极以钛酸锂为主要活性物质的非对称磷酸铁锂电池。包括正极、负极、隔膜和电解液，所述正极的主要活性物质为磷酸铁锂粉末、添加活性炭的磷酸铁锂粉末或添加碳纳米管的磷酸铁锂粉末，正极材料还包括粘结剂、导电剂和分散剂；所述负极的主要活性物质为钛酸锂粉末、添加碳纳米管的钛酸锂粉末、复合铜、银或碳纳米管的钛酸锂粉末或半导改性的钛酸锂粉末，负极材料还包括粘结剂、导电剂和分散剂。所述粘结剂为聚偏氟乙烯，所述导电剂为乙炔黑，所述分散剂为N－甲基吡咯烷酮。本发明在大电流下的充放电性能好，可以在快速充放电下同时保持高比功率和高比能量。
The invention discloses an asymmetric lithium iron phosphate battery whose negative electrode uses lithium titanate as the main active material and belongs to the technical field of lithium ion batteries or hybrid batteries of non-aqueous electrolytes. Including positive electrode, negative electrode, diaphragm and electrolyte, the main active material of the positive electrode is lithium iron phosphate powder, lithium iron phosphate powder added with activated carbon or lithium iron phosphate powder added with carbon nanotubes, the positive electrode material also includes binder, conductive agent and dispersant; the main active material of the negative electrode is lithium titanate powder, lithium titanate powder added with carbon nanotubes, lithium titanate powder compounded with copper, silver or carbon nanotubes, or semiconducting modified lithium titanate Powder, negative electrode material also includes binder, conductive agent and dispersant. The binder is polyvinylidene fluoride, the conductive agent is acetylene black, and the dispersant is N-methylpyrrolidone. The invention has good charging and discharging performance under high current, and can simultaneously maintain high specific power and high specific energy under fast charging and discharging.
Description
Technical field
The invention belongs to the lithium ion battery or the hybrid battery technical field of nonaqueous electrolytic solution, particularly a kind of negative pole is the asymmetric ferric phosphate lithium cell of main active substances with the lithium titanate.
Background technology
The lithium titanate of spinel structure is " a zero strain material ", have the excellent cyclical stability and the useful life of overlength, also having good, the safe and specific capacity of anti-over-charging performance and thermal stability simultaneously, big (theoretical specific capacity is 175mAh/g, actual specific capacity can reach 165mAh/g) etc. characteristics, be a kind of novel battery material of excellence.
The olivine-type LiFePO4 is made the positive electrode of lithium ion battery and is reported in 1997 by Goodenough research group at first, this material because have cheap, nontoxic, nonhygroscopic, Environmental compatibility is fine, rich in mineral resources, the battery circulation volume is higher, and (theoretical capacity is 170mAh/g, energy density is 550Wh/kg), stability characteristics such as fine, by vast researcher is paid close attention to.But the charge/discharge capacity of LiFePO4 under high current density is very low.
Make the charge/discharge capacity of battery under high current density of active material in order to improve LiFePO4, adopt the notion of hybrid battery.Along with the development of lithium-ion electric pool technology, the Amatucci of calendar year 2001 U.S. Telcordia Technologies company has reported the AC/Li of active carbon and the combination of lithium ion battery intercalation materials of li ions
4Ti
5O
12Asymmetric hybrid battery uses nonaqueous electrolytic solution, and positive and negative electrode relies on Faraday pseudo-capacitance and lithium ion to embed/take off the machine-processed energy storage of embedding respectively.This prototype battery charging and discharging speed and cyclical stability and ultracapacitor are similar, and energy density has reached 20Wh/kg, is higher than common ultracapacitor.When hybrid battery uses battery and capacitor electrode material at the same time, combine the big and big advantage of power density of energy density that these two kinds of traditional energy storage devices have.In contrast to other new forms of energy device, such as fuel cell and solar cell, hybrid battery has more advantage based on traditional energy storage technology development of maturation.
Summary of the invention
The purpose of this invention is to provide the asymmetric ferric phosphate lithium cell that a kind of negative pole is main active substances with the lithium titanate.
A kind of negative pole is the asymmetric ferric phosphate lithium cell of main active substances with the lithium titanate, comprise positive pole, negative pole, barrier film and electrolyte, it is characterized in that, the main active substances of described positive pole is an iron phosphate powder, add the iron phosphate powder of active carbon or the iron phosphate powder of interpolation carbon nano-tube, positive electrode also comprises binding agent, conductive agent and dispersant, wherein, each material proportion is closed and is active carbon or carbon nano-tube: iron phosphate powder: binding agent: conductive agent: g:(8～10 dispersant=(0～30) g:(50～80)) g:(10～12) g:(0.6～0.8) L; The main active substances of described negative pole is the lithium titanate powder of lithium titanate powder, lithium titanate powder, complex copper, silver or the carbon nano-tube of adding carbon nano-tube or the lithium titanate powder of partly leading modification, negative material also comprises binding agent, conductive agent and dispersant, wherein, each material proportion is closed and is copper, silver or carbon nano-tube: lithium titanate powder: binding agent: conductive agent: g:(8～10 dispersant=(0～30) g:(50～80)) g:(10～12) g:(0.6～0.8) L.
Described binding agent is a Kynoar.
Described conductive agent is an acetylene black.
Described dispersant is the N-methyl pyrrolidone.
Described complex copper, the potassium titanate powder of silver or carbon nano-tube is at the lithium titanate powder of particle surface clad metal silver or copper or be wound with the lithium titanate nanotube of carbon nano-tube, wherein, the lithium titanate powder of compound silver or copper is by lithium titanate powder and liquor argenti nitratis ophthalmicus or copper-bath, acetaldehyde or hydrazine hydrate, and ammoniacal liquor prepares by chemical deposition, the lithium titanate nanotube of composite carbon nanometer tube is with titanium dioxide, sodium hydroxide solution and salpeter solution are that raw material is when carrying out Hydrothermal Preparation lithium titanate nanotube, carbon nano-tube is added in the reactor with raw material, obtains the lithium titanate nanotube of composite carbon nanometer tube.
Described lithium titanate powder of partly leading modification is for being raw material with metatitanic acid and titanium dioxide, mixture was calcined 3～5 hours at 700～850 ℃ behind ball milling, product after reaction finishes under nitrogen atmosphere through 300～500 ℃ of heat treatments 2～4 hours, with stove cooling, the lithium titanate powder of partly being led modification.
Described iron phosphate powder is the olivine-type iron phosphate powder.
Described lithium titanate powder is the spinel type lithium titanate powder.
Beneficial effect of the present invention is: the battery among the present invention is asymmetric hybrid battery, anodal main active substances is an iron phosphate powder, add the iron phosphate powder of active carbon or the iron phosphate powder of interpolation carbon nano-tube, the main active substances of negative pole is a potassium titanate powder, add the lithium titanate powder of carbon nano-tube, complex copper, the lithium titanate powder of silver or carbon nano-tube or the lithium titanate powder of partly leading modification, mix the hybrid battery of the LiFePO4 of active carbon as positive pole, its charge-discharge performance under the big electric current than existing be that the charge-discharge performance of capacitor under big electric current of electrode is good with active carbon and lithium titanate, can under fast charging and discharging, keep high-specific-power and high-energy-density simultaneously, be fit to be applied in aspects such as electric automobile.
Description of drawings
Fig. 1 is the charging/discharging voltage curve of the hybrid battery of assembling among the embodiment 1;
Fig. 2 is the constant current charge-discharge cycle performance curve of the hybrid battery of assembling among the embodiment 1;
Fig. 3 is the cyclic voltammetry curve of the hybrid battery of assembling among the embodiment 1;
Fig. 4 is a charging/discharging voltage curve of executing the hybrid battery of assembling in the example 2;
Fig. 5 is the constant current charge-discharge cycle performance curve of the hybrid battery of assembling among the embodiment 2;
Fig. 6 is the charging/discharging voltage curve of the hybrid battery of assembling among the embodiment 3;
Fig. 7 is the constant current charge-discharge cycle performance curve of the hybrid battery of assembling among the embodiment 3;
Fig. 8 is the charging/discharging voltage curve of the hybrid battery of assembling among the embodiment 4;
Fig. 9 is the constant current charge-discharge cycle performance curve of the hybrid battery of assembling among the embodiment 4.
Embodiment
The invention will be further described below in conjunction with accompanying drawing:
Embodiment 1
The preparation of iron phosphate powder is with reference to " a kind of polycrystalline LiFePO of olivine structural
4Powder preparation method " (publication number: CN1410349) with " a kind of LiFePO
4The preparation method of spherical powder " (publication number: CN1648036), iron phosphate powder adopts following method preparation: at first press LiFePO
4In the mole proportioning of each atom, 0.5:1:1 takes by weighing raw material Li in molar ratio
2CO
3, Fe (CO
2)
22H
2O and NH
4H
2PO
4, with raw material ball milling 6 hours and oven dry, about 400 ℃ of The pre-heat treatment are 8 hours under the weakly reducing atmosphere environment, take out after cooling to room temperature with the furnace, and secondary ball milling 6 hours, dry, sieve.For the tap density that increases material to improve the battery volume energy density, powder is carried out mist projection granulating, put it into porcelain boat subsequently, 700 ℃ of roastings 8 hours, take out after cooling to room temperature with the furnace, obtain the LiFePO of olivine structural
4Powder (particle diameter is about 5～20 μ m).
A kind of negative pole is the asymmetric ferric phosphate lithium cell of main active substances with the lithium titanate, comprise positive pole, negative pole, barrier film and electrolyte, the main active substances of described positive pole is for adding the olivine-type iron phosphate powder of active carbon, positive electrode also comprises binding agent, conductive agent and dispersant, wherein, each material proportion is closed, active carbon: iron phosphate powder: binding agent: conductive agent: dispersant=30g:50g:10g:10g:0.7L, described binding agent is a Kynoar, described conductive agent is an acetylene black, and described dispersant is the N-methyl pyrrolidone.Get the LiFePO of the spherical olivine structural of above-mentioned preparation
4Powder (particle diameter is about 5～20 μ m) 2.5g, specific area is about 1500m
2The active carbon 1.5g of/g, binding agent Kynoar (PVDF) 0.5g and conductive agent acetylene black 0.5g, mix the back and add dispersant N-methyl pyrrolidone (NMP) 35ml, stirred 4 hours, on aluminium foil, carry out curtain coating with scraping the skill in using a kitchen knife in cookery then, and place 120 ℃ of following vacuum to obtain anodal diaphragm after dry 1.5 hours.
The main active substances of described negative pole is that the spinel type lithium titanate powder is (commercially available, the lithium titanate powder is a nanoscale, average grain diameter is about 500nm), negative material also comprises binding agent, conductive agent and dispersant, and wherein, each material proportion is closed and is, lithium titanate powder: binding agent: conductive agent: dispersant=80g:10g:10g:0.8L, described binding agent is a Kynoar, and described conductive agent is an acetylene black, and described dispersant is the N-methyl pyrrolidone.Get spinel-type Li
4Ti
5O
12Powder 4.8g, binding agent Kynoar (PVDF) 0.6g and conductive agent acetylene black 0.6g, mix the back and add dispersant N-methyl pyrrolidone (NMP) 48ml, stirred 4 hours, on aluminium foil, carry out curtain coating with scraping the skill in using a kitchen knife in cookery then, and place 120 ℃ of following vacuum to obtain cathode membrane after dry 1.5 hours.
The process of assembling test battery: with positive and negative electrode diaphragm diameter is 12 millimeters drift punching, with assembling CR2032 type button test battery, adopts 1mol/L lithium hexafluoro phosphate (LiPF
6) mixed liquor in ethylene carbonate (EC) and dimethyl carbonate (DMC) (volume ratio of ethylene carbonate and dimethyl carbonate is 1:1) is as electrolyte, it is the barrier film of Sai Er Goethe 2400 (Celgard 2400) that barrier film adopts the U.S. to produce model, packaged battery carries out in the glove box of argon gas atmosphere, makes hybrid battery.
The hybrid battery of present embodiment preparation obtains the charging/discharging voltage curve as shown in Figure 1 through the constant current charge-discharge test, and charge and discharge process comprises A-B, B-C, C-D, E-F, F-G, six processes of G-H.In the A-B stage, along with the carrying out of constant current charge, system voltage constantly raises, and when voltage is elevated to the 1.8V left and right sides, is the B-C stage, and charging is proceeded, and that cell voltage keeps substantially is constant, this moment Li
+Constantly from anodal LiFePO
4In spin off, embed negative pole Li
4Ti
5O
12In.C-D is the last stage of charging, at this moment Li
+Deviate from totally or owing to the reason Li of voltage polarizing
+Can not continue to deviate from from material, in this stage, the voltage of hybrid battery raises along with the rising of specific capacity, is similar to linear relationship, and final charging process finishes.The E-H stage is the discharge overall process, E-F wherein, and F-G, G-H are respectively C-D, the inverse process of B-C and A-B.The constant current charge-discharge cycle performance as shown in Figure 2, along with the raising of charge-discharge magnification, the capacity of battery descends thereupon.Under identical charge-discharge magnification, the circulation repeatedly capacity of back battery also can descend slightly.Discharge capacity in preceding 10 circulations is starkly lower than the charging capacity, and the discharging efficiency of battery in back tens circulations is all more than 95%.Record cyclic voltammetry curve as shown in Figure 3 through cyclic voltammetry, sweep limits is 1.0-3.5V, and sweep speed is 0.01V/s.Hybrid battery is the Faraday pseudo-capacitance characteristic, at 1.5V and 2.2V a pair of redox peak than broad is arranged.
Embodiment 2
A kind of negative pole is the asymmetric ferric phosphate lithium cell of main active substances with the lithium titanate, comprise positive pole, negative pole, barrier film and electrolyte, the main active substances of described positive pole is for adding the olivine-type iron phosphate powder of active carbon, positive electrode also comprises binding agent, conductive agent and dispersant, wherein, each material proportion is closed, active carbon: iron phosphate powder: binding agent: conductive agent: dispersant=10g:70g:10g:10g:0.7L, described binding agent is a Kynoar, described conductive agent is an acetylene black, and described dispersant is the N-methyl pyrrolidone.Get the LiFePO of spherical olivine structural
4Powder (LiFePO
4Powder diameter is about 5～20 μ m, and the preparation method is identical with embodiment 1) 3.5g, specific area is about 1500m
2The active carbon 0.5g of/g, binding agent Kynoar (PVDF) 0.5g and conductive agent acetylene black 0.5g, mix the back and add dispersant N-methyl pyrrolidone (NMP) 35ml, stirred 4 hours, on aluminium foil, carry out curtain coating with scraping the skill in using a kitchen knife in cookery then, and place 120 ℃ of following vacuum to obtain anodal diaphragm after dry 1.5 hours.
The main active substances of described negative pole is the spinel type lithium titanate powder of partly leading modification, (with metatitanic acid and titanium dioxide is raw material, mixture was calcined 4 hours at 800 ℃ behind ball milling, product after reaction finishes under nitrogen atmosphere through 400 ℃ of heat treatments 2 hours, cool off with stove, partly led the lithium titanate powder of modification, the lithium titanate powder of partly leading modification is a nanoscale, average grain diameter is about 500nm), negative material also comprises binding agent, conductive agent and dispersant, wherein, it is that lithium titanate powder: binding agent: conductive agent: dispersant=80g:10g:10g:0.8L, described binding agent are Kynoar that each material proportion is closed, described conductive agent is an acetylene black, and described dispersant is the N-methyl pyrrolidone.Learn from else's experience nitrogen atmosphere second lead the spinel-type Li of modification
4Ti
5O
12Powder 4.8g, binding agent Kynoar (PVDF) 0.6g and conductive agent acetylene black 0.6g, mix the back and add dispersant N-methyl pyrrolidone (NMP) 48ml, stirred 4 hours, on aluminium foil, carry out curtain coating with scraping the skill in using a kitchen knife in cookery then, and place 120 ℃ of following vacuum to obtain cathode membrane after dry 1.5 hours.
The process of assembling test battery: with positive and negative electrode diaphragm diameter is 12 millimeters drift punching, with assembling CR2032 type button test battery, adopts 1mol/L lithium hexafluoro phosphate (LiPF
6) mixed liquor in ethylene carbonate (EC) and dimethyl carbonate (DMC) (volume ratio of ethylene carbonate and dimethyl carbonate is 1:1) is as electrolyte, it is the barrier film of Sai Er Goethe 2400 (Celgard 2400) that barrier film adopts the U.S. to produce model, packaged battery carries out in the glove box of argon gas atmosphere, obtains (the LiFePO that positive pole contains 10% active carbon
4-AC)/Li
4Ti
5O
12Hybrid battery.
The hybrid battery for preparing in the present embodiment obtains the charging/discharging voltage curve as shown in Figure 4 through the constant current charge-discharge test, and similar with Fig. 1, charge and discharge process also comprises A-B, B-C, C-D, E-F, F-G, six processes of G-H, E-F wherein, F-G, G-H are respectively C-D, the inverse process of B-C and A-B.As can be seen, the battery in the embodiment 1, the voltage platform of this battery is longer more flat.The constant current charge-discharge cycle performance as shown in Figure 5, and is similar with Fig. 2, and along with the raising of charge-discharge magnification, the capacity of battery descends thereupon.Under identical charge-discharge magnification, the circulation repeatedly capacity of back battery also can descend slightly.Discharge capacity in preceding 10 circulations is starkly lower than the charging capacity, and the discharging efficiency of battery in back tens circulations is all more than 95%.
Embodiment 3
A kind of negative pole is the asymmetric ferric phosphate lithium cell of main active substances with the lithium titanate, comprise positive pole, negative pole, barrier film and electrolyte, the main active substances of described positive pole is the olivine-type iron phosphate powder, positive electrode also comprises binding agent, conductive agent and dispersant, wherein, each material proportion is closed, iron phosphate powder: binding agent: conductive agent: dispersant=80g:10g:10g:0.67L, described binding agent is a Kynoar, described conductive agent is an acetylene black, and described dispersant is the N-methyl pyrrolidone.Get the LiFePO of spherical olivine structural
4Powder (LiFePO
4Powder diameter is about 5～20 μ m, the preparation method is identical with embodiment 1) 4.8g, binding agent Kynoar (PVDF) 0.6g and conductive agent acetylene black 0.6g, mix the back and add dispersant N-methyl pyrrolidone (NMP) 40ml, stirred 4 hours, on aluminium foil, carry out curtain coating with scraping the skill in using a kitchen knife in cookery then, and place 120 ℃ of following vacuum to obtain anodal diaphragm after dry 1.5 hours.
The main active substances of described negative pole is that (with metatitanic acid and titanium dioxide is raw material for the spinel type lithium titanate powder of compound silver, mixture was calcined 4 hours at 800 ℃ behind ball milling, obtaining the lithium titanate powder, is the spinel-type Li of 0.01mol/L liquor argenti nitratis ophthalmicus, pH value compound 8% (weight) silver that to be 8～9 weak aqua ammonia and acetaldehyde obtain by chemical deposition with lithium titanate powder and concentration
4Ti
5O
12Powder, the spinel type lithium titanate powder of the compound silver that obtains is a nanoscale, average grain diameter is 500nm), negative material also comprises binding agent, conductive agent and dispersant, and wherein, each material proportion is closed and is, silver: lithium titanate powder: binding agent: conductive agent: dispersant=6.4:73.6g:10g:10g:0.8L, described binding agent is a Kynoar, and described conductive agent is an acetylene black, and described dispersant is the N-methyl pyrrolidone.Get the spinel-type Li of compound silver
4Ti
5O
12Powder 4.8g, binding agent Kynoar (PVDF) 0.6g and conductive agent acetylene black 0.6g, mix the back and add dispersant N-methyl pyrrolidone (NMP) 48ml, stirred 4 hours, on aluminium foil, carry out curtain coating with scraping the skill in using a kitchen knife in cookery then, and place 120 ℃ of following vacuum to obtain cathode membrane after dry 1.5 hours.
The process of assembling test battery: with positive and negative electrode diaphragm diameter is 12 millimeters drift punching, with assembling CR2032 type button test battery, adopts 1mol/L lithium hexafluoro phosphate (LiPF
6) mixed liquor in ethylene carbonate (EC) and dimethyl carbonate (DMC) (volume ratio of ethylene carbonate and dimethyl carbonate is 1:1) is as electrolyte, it is the barrier film of Sai Er Goethe 2400 (Celgard 2400) that barrier film adopts the U.S. to produce model, packaged battery carries out in the glove box of argon gas atmosphere, obtains the anodal LiFePO that does not contain active carbon
4/ Li
4Ti
5O
12Hybrid battery.
The hybrid battery for preparing in the present embodiment obtains the charging/discharging voltage curve as shown in Figure 6 through the constant current charge-discharge test, and similar with Fig. 4, charge and discharge process also comprises A-B, B-C, C-D, E-F, F-G, six processes of G-H, E-F wherein, F-G, G-H are respectively C-D, the inverse process of B-C and A-B.Owing to added carbon nano-tube, the voltage platform of battery is not a definite value, but at 1.5V between the 1.9V.The constant current charge-discharge cycle performance as shown in Figure 7, and is similar with Fig. 5, and along with the raising of charge-discharge magnification, the capacity of battery descends thereupon.Under identical charge-discharge magnification, the circulation repeatedly capacity of back battery also can descend slightly.Discharge capacity in preceding 10 circulations is starkly lower than the charging capacity, and the discharging efficiency of battery in back tens circulations is all more than 95%.
Embodiment 4
The preparation method of lithium titanate nanotube is with reference to " the spinel lithium titanate nanotube/line preparation method who is used for lithium battery and capacitor " (publication number: CN1725530): with 5g TiO
2With 70mL concentration is that the NaOH solution of 10m/L mixes, and is 0.2～0.5W/cm at power
2Following sonochemistry reaction 30 minutes, to move into volume then be 100mL, have in the autoclave of teflon lined and carried out hydro-thermal reaction 24 hours, hydrothermal temperature is 150 ℃, after reaction finishes, takes out reactor, naturally cool to room temperature, filtering after opening kettle cover, is that the product to hydro thermal method washed 30 minutes under 2 the condition at pH with the nitric acid of 0.2mol/L concentration, behind the vacuum filtration, product obtains the fluffy powder product of white after 80 ℃ of dryings, be H
2Ti
3O
7Nanotube; With 1.5gH
2Ti
3O
7Nanotube and 40mLLiOH aqueous solution, stir, to move into volume then be 50mL, have in the autoclave of teflon lined and carry out more than the hydro-thermal reaction 24h, preparation nanotube hydrothermal temperature is 100～150 ℃, after reaction finishes, take out reactor, naturally cool to room temperature, filter after opening kettle cover, with deionized water wash for several times, behind the vacuum filtration, filter cake with absolute ethanol washing for several times, product obtains the product of white after 80 ℃ of vacuumize, white product obtains having spinel-type Li through 400 ℃ of heat treatments after 2 hours in air atmosphere
4Ti
5O
12Nanotube, its external diameter is about 10nm, and internal diameter is 4～5nm, is about the hundreds of nanometer to micron order.
A kind of negative pole is the asymmetric ferric phosphate lithium cell of main active substances with the lithium titanate, comprise positive pole, negative pole, barrier film and electrolyte, the main active substances of described positive pole is the olivine-type iron phosphate powder, positive electrode also comprises binding agent, conductive agent and dispersant, wherein, each material proportion is closed, iron phosphate powder: binding agent: conductive agent: dispersant=80g:10g:10g:0.6L, described binding agent is a Kynoar, described conductive agent is an acetylene black, and described dispersant is the N-methyl pyrrolidone.Get the LiFePO of spherical olivine structural
4Powder (LiFePO
4The preparation method of powder is identical with embodiment 1) 4.0g, binding agent Kynoar (PVDF) 0.5g and conductive agent acetylene black 0.5g, mix the back and add dispersant N-methyl pyrrolidone (NMP) 30ml, stirred 4 hours, on aluminium foil, carry out curtain coating with scraping the skill in using a kitchen knife in cookery then, and place 120 ℃ of following vacuum to obtain anodal diaphragm after dry 1.5 hours.
The main active substances of described negative pole is spinel type lithium titanate powder (a lithium titanate nanotube), negative material also comprises binding agent, conductive agent and dispersant, wherein, each material proportion is closed, lithium titanate powder: binding agent: conductive agent: dispersant=80g:10g:10g:0.8L, described binding agent is a Kynoar, and described conductive agent is an acetylene black, and described dispersant is the N-methyl pyrrolidone.Get the spinel-type Li that adopts method for preparing
4Ti
5O
12(its external diameter is about 10nm to lithium titanate nanotube 4.0g, internal diameter is 4～5nm, be about the hundreds of nanometer to micron order), binding agent Kynoar (PVDF) 0.5g and conductive agent acetylene black 0.5g, mix the back and add dispersant N-methyl pyrrolidone (NMP) 40ml, carry out ultrasonicly in supersonic generator, ultrasonic power is 0.2～0.5W/cm
2, 1 hour time, stirred then 4 hours, on aluminium foil, carry out curtain coating with scraping the skill in using a kitchen knife in cookery then, and place 120 ℃ of following vacuum to obtain cathode membrane after dry 1.5 hours.
The process of assembling test battery: with positive and negative electrode diaphragm diameter is 12 millimeters drift punching, with assembling CR2032 type button test battery, adopts 1mol/L lithium hexafluoro phosphate (LiPF
6) mixed liquor in ethylene carbonate (EC) and dimethyl carbonate (DMC) (volume ratio of ethylene carbonate and dimethyl carbonate is 1:1) is as electrolyte, it is the barrier film of Sai Er Goethe 2400 (Celgard 2400) that barrier film adopts the U.S. to produce model, packaged battery carries out in the glove box of argon gas atmosphere, obtains negative pole and uses Li
4Ti
5O
12The LiFePO of nanotube
4/ Li
4Ti
5O
12Hybrid battery.
The hybrid battery for preparing in the present embodiment obtains the charging/discharging voltage curve as shown in Figure 8 through the constant current charge-discharge test, and similar with Fig. 6, charge and discharge process also comprises A-B, B-C, C-D, E-F, F-G, six processes of G-H, E-F wherein, F-G, G-H are respectively C-D, the inverse process of B-C and A-B.Because negative pole adopts the lithium titanate nanotube, the voltage platform of battery is not a definite value, but at 1.5V between the 2.2V.The constant current charge-discharge cycle performance as shown in Figure 9, and is similar with Fig. 7, and along with the raising of charge-discharge magnification, the capacity of battery descends thereupon.Under identical charge-discharge magnification, the circulation repeatedly capacity of back battery also can descend slightly.
Claims (8)
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| CN101789315A (en) * | 2010-03-19 | 2010-07-28 | 常州康维电子科技有限公司 | Hybrid super capacitor and preparation method thereof |
| CN102201565A (en) * | 2011-04-14 | 2011-09-28 | 杭州万好万家动力电池有限公司 | High-capacity metal lithium powder composite cathode and preparation method thereof, and multi-layer composite electrode |
| CN102502799A (en) * | 2011-11-11 | 2012-06-20 | 东莞市迈科科技有限公司 | A modification method of commercial spinel lithium titanate and its product |
| CN102544438A (en) * | 2010-12-20 | 2012-07-04 | 梅岭化工厂 | Lithium titanate electrode doped with nanometer silver powder for lithium ion battery and preparation method for electrode |
| CN102903930A (en) * | 2012-10-23 | 2013-01-30 | 中国科学院过程工程研究所 | A kind of lithium ion secondary battery and preparation method thereof |
| CN103280554A (en) * | 2013-05-22 | 2013-09-04 | 南京双登科技发展研究院有限公司 | Paste mixing process of lithium titanate battery |
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| CN103531773A (en) * | 2013-10-30 | 2014-01-22 | 合肥恒能新能源科技有限公司 | Compound lithium titanate negative-electrode material and preparation method thereof |
| CN103531767A (en) * | 2013-10-30 | 2014-01-22 | 合肥恒能新能源科技有限公司 | Lithium battery special-purpose modified lithium titanate negative electrode material and preparation method thereof |
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| CN103545499A (en) * | 2013-10-30 | 2014-01-29 | 合肥恒能新能源科技有限公司 | Carbon black-modified lithium titanate negative electrode material as well as preparation method thereof |
| CN103560239A (en) * | 2013-10-30 | 2014-02-05 | 合肥恒能新能源科技有限公司 | Graphite-modified lithium titanate negative electrode material and preparation method thereof |
| CN103682278A (en) * | 2013-12-26 | 2014-03-26 | 山东精工电子科技有限公司 | Preparation method of nanocarbon coated lithium titanate cathode material |
| CN103825008A (en) * | 2014-03-21 | 2014-05-28 | 中国科学院新疆理化技术研究所 | Preparation method of three-dimensional porous lithium battery positive plate |
| CN104733710A (en) * | 2015-03-03 | 2015-06-24 | 深圳市翔丰华科技有限公司 | Lithium titanate negative electrode material and preparation method thereof |
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| CN107658448A (en) * | 2017-09-15 | 2018-02-02 | 江汉大学 | The preparation method of zero strain hydridization LTO lithium cell cathode materials and the cathode of lithium battery containing the negative material |
| CN108199077A (en) * | 2017-12-29 | 2018-06-22 | 天津市捷威动力工业有限公司 | A kind of lithium ion battery with Good Security and preparation method thereof |
| CN111533107A (en) * | 2020-05-08 | 2020-08-14 | 蒋达金 | Preparation method of lithium cobalt phosphate-lithium vanadium phosphate composite positive electrode material |
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| CN101789315A (en) * | 2010-03-19 | 2010-07-28 | 常州康维电子科技有限公司 | Hybrid super capacitor and preparation method thereof |
| CN101789315B (en) * | 2010-03-19 | 2013-03-13 | 苏州能斯特新能源有限公司 | Hybrid super capacitor and preparation method thereof |
| CN102544438A (en) * | 2010-12-20 | 2012-07-04 | 梅岭化工厂 | Lithium titanate electrode doped with nanometer silver powder for lithium ion battery and preparation method for electrode |
| CN102201565A (en) * | 2011-04-14 | 2011-09-28 | 杭州万好万家动力电池有限公司 | High-capacity metal lithium powder composite cathode and preparation method thereof, and multi-layer composite electrode |
| CN102201565B (en) * | 2011-04-14 | 2013-11-06 | 美国电化学动力公司 | High-capacity metal lithium powder composite cathode and preparation method thereof, and multi-layer composite electrode |
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| CN102903930A (en) * | 2012-10-23 | 2013-01-30 | 中国科学院过程工程研究所 | A kind of lithium ion secondary battery and preparation method thereof |
| CN102903930B (en) * | 2012-10-23 | 2016-06-08 | 中国科学院过程工程研究所 | A kind of lithium rechargeable battery and preparation method thereof |
| CN103280554A (en) * | 2013-05-22 | 2013-09-04 | 南京双登科技发展研究院有限公司 | Paste mixing process of lithium titanate battery |
| CN103531769A (en) * | 2013-10-30 | 2014-01-22 | 合肥恒能新能源科技有限公司 | Lithium battery modified lithium titanate negative electrode material and preparation method thereof |
| CN103531768A (en) * | 2013-10-30 | 2014-01-22 | 合肥恒能新能源科技有限公司 | Doped modified lithium titanate negative electrode material and preparation method thereof |
| CN103531774A (en) * | 2013-10-30 | 2014-01-22 | 合肥恒能新能源科技有限公司 | Modified lithium titanate negative electrode material made of nanometer material and preparing method thereof |
| CN103531773A (en) * | 2013-10-30 | 2014-01-22 | 合肥恒能新能源科技有限公司 | Compound lithium titanate negative-electrode material and preparation method thereof |
| CN103545499A (en) * | 2013-10-30 | 2014-01-29 | 合肥恒能新能源科技有限公司 | Carbon black-modified lithium titanate negative electrode material as well as preparation method thereof |
| CN103560239A (en) * | 2013-10-30 | 2014-02-05 | 合肥恒能新能源科技有限公司 | Graphite-modified lithium titanate negative electrode material and preparation method thereof |
| CN103531767A (en) * | 2013-10-30 | 2014-01-22 | 合肥恒能新能源科技有限公司 | Lithium battery special-purpose modified lithium titanate negative electrode material and preparation method thereof |
| CN103682278A (en) * | 2013-12-26 | 2014-03-26 | 山东精工电子科技有限公司 | Preparation method of nanocarbon coated lithium titanate cathode material |
| CN103682278B (en) * | 2013-12-26 | 2016-05-11 | 山东精工电子科技有限公司 | The preparation method of the coated lithium titanate anode material of a kind of nanometer carbon |
| CN103825008A (en) * | 2014-03-21 | 2014-05-28 | 中国科学院新疆理化技术研究所 | Preparation method of three-dimensional porous lithium battery positive plate |
| CN103825008B (en) * | 2014-03-21 | 2016-01-13 | 中国科学院新疆理化技术研究所 | A method for preparing a three-dimensional porous lithium battery cathode |
| CN104733710A (en) * | 2015-03-03 | 2015-06-24 | 深圳市翔丰华科技有限公司 | Lithium titanate negative electrode material and preparation method thereof |
| CN104882611A (en) * | 2015-04-01 | 2015-09-02 | 广东烛光新能源科技有限公司 | An electrochemical anode electrode, an energy storage device comprising the anode electrode, and a preparation method thereof |
| CN104882611B (en) * | 2015-04-01 | 2017-12-08 | 广东烛光新能源科技有限公司 | A kind of Anodic electrode, energy storage device comprising the anode electrode and preparation method thereof |
| WO2016202173A1 (en) * | 2015-06-15 | 2016-12-22 | 山东玉皇新能源科技有限公司 | Method for preparing high-purity lithium titanate negative electrode material and use thereof |
| CN107658448A (en) * | 2017-09-15 | 2018-02-02 | 江汉大学 | The preparation method of zero strain hydridization LTO lithium cell cathode materials and the cathode of lithium battery containing the negative material |
| CN108199077A (en) * | 2017-12-29 | 2018-06-22 | 天津市捷威动力工业有限公司 | A kind of lithium ion battery with Good Security and preparation method thereof |
| CN111533107A (en) * | 2020-05-08 | 2020-08-14 | 蒋达金 | Preparation method of lithium cobalt phosphate-lithium vanadium phosphate composite positive electrode material |
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