CN100364167C - Chargeable lithium cell and preparing method - Google Patents
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- CN100364167C CN100364167C CNB021524270A CN02152427A CN100364167C CN 100364167 C CN100364167 C CN 100364167C CN B021524270 A CNB021524270 A CN B021524270A CN 02152427 A CN02152427 A CN 02152427A CN 100364167 C CN100364167 C CN 100364167C
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Abstract
This invention disclosed a chargeable lithium battery, which includes an anode and a cathode that can be embedded and extricated themself from the lithium, and an electrolyte which contains a polyacrylate with three or more acrylic groups.
Description
The cross reference of<this application 〉
The application based on and require to submit to December 3 calendar year 2001 the priority of Japanese patent application 2001-369366 number of Japan Patent office, its disclosed content is incorporated herein by reference.
Technical field
The present invention relates to a kind of rechargeable lithium battary and preparation method thereof.
Background technology
Along with the increase of the use of portable electric appts such as portable phone, portable video camera and notebook computer, the needs of high-energy-density lithium battery are increased day by day.Particularly, when charging the battery, if negative pole has electronegative potential, then it tends to decompose electrolyte, so battery performance key element such as capacity, capacity reservation, cycle life characteristics and cryogenic property worsen.Therefore, prevent that importantly negative pole and electrolyte from reacting, so that improve the battery performance of chargeable lithium cell with electrolyte organic solution or polyelectrolyte.
Should consider the reactivity of itself and negative pole when selecting electrolyte material.The a lot of solvent that is used for electrolyte and mixtures that do not react with negative pole have been proposed.Except non-reacted, when selecting the solvent of electrolyte, also should be taken into account the solubility that supports salt (supporting salt), with anodal reactivity, ionic conductivity and cost.
The examples of non-aqueous that is used for chargeable lithium cell that has proposed comprises ethylene carbonate, butylene carbonate, dimethyl carbonate, methyl ethyl carbonate, diethyl carbonate, gamma-butyrolacton, methyl propionate, butyl propionate, ethyl propionate and their mixture.
The another kind of approach of having attempted is to suppress reaction between negative pole and the electrolyte by add some compound in electrolyte, and then improves the performance of battery.But this mixture causes adverse influence to charging and exoelectrical reaction, and is difficult to the voltage and current that provides required in the battery.
Japanese Patent Application Publication discloses the battery that lithium or lithium metal could be sneaked into and deviate to a kind of negative material for 1996-96852 number, and nonaqueous solvents wherein is made up of vinylene carbonate.But, still can not expect to improve the battery performance that negative pole is a carbonaceous material, because vinylene carbonate can not be coated with negative pole fully.
When adding vinylene carbonate, produce excessive gas, and the battery distortion.The generation that it is believed that gas be owing to the coating in charging for the first time form during the decomposition of electrolyte cause.Electrolyte causes the weakening of battery performance because of the generation sex change of gas.
Summary of the invention
In one embodiment, the invention provides and comprise positive pole, negative pole and electrolyte rechargeable lithium battary.This electrolyte comprises the many acrylate compounds with three or more acrylic acid groups.
The present invention also provides the chargeable lithium cell that comprises positive pole, negative pole and electrolyte, wherein should positive pole and negative pole can embed and deviate from lithium.Electrolyte is to form by the polymer that electrolyte organic solution is flooded many acrylate compounds, and negative terminal surface has been coated with the organic coating of many acrylate compounds.These many acrylate compounds are the compound with three or more acrylic acid groups.
The present invention also provides and comprises positive pole, negative pole and comprise the chargeable lithium cell that electrolyte organic solution is the electrolyte of main component.Negative terminal surface has been coated with the organic coating of the many acrylate compounds with three or more acrylic acid groups.
The present invention also provides a kind of method for preparing chargeable lithium cell, this battery comprises positive pole and the negative pole and the electrolyte that can embed and deviate from lithium, wherein this method comprises that the many acrylate compounds that will have three or more acrylic acid groups are added in the electrolyte, and this electrolyte is placed between positive pole and the negative pole.This method may further include subsequently 40~120 ℃ down heating place electrolyte between the electrode.
Description of drawings
With reference to following specific descriptions also in conjunction with the accompanying drawings, the lot of advantages that can more completely understand the present invention and be followed, in the accompanying drawings:
Fig. 1 is the curve chart that concerns between the period of battery of the explanation embodiment of the invention 11 and Comparative Examples 2 and the discharge capacity; With
Fig. 2 is the curve chart that concerns between the period of battery of the explanation embodiment of the invention 12 and Comparative Examples 3 and the discharge capacity.
Embodiment
In following specifying, only provide and illustrated the preferred embodiments of the invention to set forth the form that the inventor finishes best mode of the present invention.Should be appreciated that the present invention can make amendment aspect conspicuous a lot, and all do not break away from the present invention.Therefore, drawing and description are indicative rather than restrictive in fact.
Chargeable lithium cell of the present invention comprises positive pole and the negative pole and the electrolyte that can embed and deviate from lithium.This electrolyte comprises the many acrylate compounds with three or more acrylic acid groups.
When the chargeable lithium cell primary charging, the polymerization of many acrylate compounds, and be formed with organic coating in negative terminal surface.Because this organic coating even the charging voltage of recharge increases, also can prevent the electrolyte decomposition of negative terminal surface.Therefore, can prevent advantageously that gas from producing and the electrolyte sex change, charge/discharge capacity does not worsen, and cycle life characteristics improves, and can prevent the battery distortion.
The content of many acrylate compounds is preferably 0.001~10% of electrolyte weight, and more preferably 0.1~5% of electrolyte weight.
Electrolyte can further include at least a in acrylonitrile and the methacrylonitrile.The content of acrylonitrile and/or methacrylonitrile is preferably 0.001~10% weight, more preferably 0.05~1% weight.
Electrolyte is to form by the polymer that electrolyte organic solution is flooded many acrylate compounds.
Negative terminal surface preferably is coated with at least a organic coating in many acrylate compounds and/or acrylonitrile and the methacrylonitrile.
Preferred many acrylate compounds chemical formula in the formula of (1)~(3) below being selected from is represented:
Wherein, 0≤a≤15,0≤b≤15,0≤c≤15,3≤a+b+c≤15.
Many acrylate compounds of formula 1 are trimethylolpropane triacrylate, have three acrylic acid groups in its molecule.Many acrylate compounds of formula 2 are trimethylolpropane tris ethyoxyl triacrylate, have three acrylic acid groups in its molecule.Many acrylate compounds of formula 3 are trimethylolpropane tris propoxyl group triacrylate, have three acrylic acid groups in its molecule.
Preferred many acrylate compounds have the dipentaerythritol structure shown in the following formula 4, and more preferably it comprises six acrylate groups shown in following formula 5:
Ac1:-CO-CH=CH
2
Ac2:-CO-(CH
2)
5-O-CO-CH=CH
2
In chargeable lithium cell of the present invention, dissolved CO in the preferred electrolyte
2
According to the present invention, preparation comprises that the method for the chargeable lithium cell of the positive pole that can embed and deviate from lithium and negative pole and electrolyte comprises that the many acrylate compounds that will have three or more acrylic acid groups are added in the electrolyte, and this electrolyte is placed between positive pole and the negative pole.This method may further include subsequently 40~120 ℃ down heating place electrolyte between the electrode.After heating steps, obtain polyelectrolyte.
In adding step, preferably when adding many acrylate compounds, also in electrolyte, add at least a in acrylonitrile and the methacrylonitrile.
Preferably during handling with CO
2Be dissolved in the electrolyte.If electrolyte had dissolved CO before it places between the electrode
2, then some lithium ions and CO near the negative pole
2Reaction forms the lithium carbonate layer, and it can compensate the reduction of ionic conductivity under the low temperature.Therefore, the cryogenic property of chargeable lithium cell is improved.
Many acrylate compounds polymerization of the present invention forms the polyelectrolyte that comprises electrolyte organic solution, and is formed with organic coating in negative terminal surface.If do not form polyelectrolyte, then the main component of electrolyte is an electrolyte organic solution.
When the content of many acrylate compounds is higher, can prepare better polymerization thing electrolyte, and when its content was low, the main component of electrolyte was electrolytical organic solution.
According to the present invention, many acrylate compounds preferably have the structure of the formula of being selected from 1~3, promptly have trifunctional group acrylate's derivative of three or more carbon-carbon double bond.But many acrylate compounds are to carry out the monomer that radical polymerization produces the anionic polymerization of polyelectrolyte by heating.In addition, when negative pole had electronegative potential during the battery charge, many acrylate compounds were formed with organic coating in negative terminal surface.When many acrylate compounds of heating, cause anionic polymerization, three or more carbon-carbon double bond is opened in the molecule, and all combines with other many acrylate molecule in chain reaction.As a result, because the negative terminal surface that is aggregated in of many acrylate compounds is formed with organic coating.
Preferred these many acrylate compounds have the dipentaerythritol structure shown in the formula 4, and more preferably it has six acrylic acid groups as shown in Equation 5.
Except many acrylate compounds, can also comprise acrylonitrile and/or methacrylonitrile according to organic coating of the present invention.Similarly, when providing many acrylate compounds separately, anionic polymerization also takes place in the negative terminal surface that has low-voltage between charge period, so, on negative pole, be coated with organic coating equally.
Although concrete structure is not confirmed, by inference, it is the copolymer of many acrylate compounds and acrylonitrile and/or methacrylonitrile.This organic coating has high lithium ion conductive, and is the durable coating of anti-electrolysis.
This organic coating is extremely thin, has several thickness to tens nanometer scale.If this thickness is several micron dimensions, then lithium ion is difficult to penetrate this coating, so be difficult to discharge and recharge reaction.When this thickness during, not preferred because the shape of coating can not get keeping less than 1 nanometer.
Because organic coating is formed at negative terminal surface, directly contacts with electrolyte so prevented negative pole.Therefore, the reproducibility of electrolyte is decomposed and to be inhibited on the negative terminal surface, so the gas that produces because of electrolyte decomposition reduces and no longer sex change of electrolyte.Owing to reduced the gas generation, the interior pressure of battery no longer increases, so not redeformation of battery.Owing to prevented the electrolyte sex change, the amount of electrolyte no longer reduces.Because discharging and recharging reacting balance ground carries out, thus the efficiency for charge-discharge increase, and cycle life characteristics improves.
Because the reaction between electrolyte and the negative pole is inhibited, so no longer sex change of electrolyte, and battery performance factor such as efficiency for charge-discharge and cycle characteristics no longer worsen, though battery at high temperature long time stored also be like this.
Because organic coating has high ionic conductivity, so it can transmit lithium ion between electrolyte and negative pole.
Although negative terminal surface has been coated with organic coating, it does not disturb the motion of lithium ion, carries out so discharge and recharge reacting balance ground, thereby efficiency for charge-discharge is improved, and cycle characteristics improves.In addition, the internal resistance of battery does not increase, and charge/discharge capacity reduces indistinctively.
The example of described electrolyte is the electrolyte organic solution that lithium salts is dissolved in nonaqueous solvents.
Examples of non-aqueous includes but not limited to propylene carbonate, ethylene carbonate, butylene carbonate, benzonitrile, acetonitrile, oxolane, the 2-methyltetrahydrofuran, gamma-butyrolacton, dioxolanes, 4-methyl dioxolanes, N, dinethylformamide, dimethylacetylamide, methyl-sulfoxide, dioxane, 1, the 2-dimethoxy-ethane, sulfolane, dichloroethanes, chlorobenzene, nitrobenzene, dimethyl carbonate, methyl ethyl carbonate, diethyl carbonate, carbonic acid first propyl ester, carbonic acid isopropyl methyl ester, carbonic acid ethyl butyl ester, dipropyl carbonate, the carbonic acid diisopropyl ester, dibutyl carbonate, diethylene glycol, dimethyl ether and their mixture, and known any conventional solvent in the chargeable lithium cell field.Preferably it comprises in propylene carbonate, ethylene carbonate or the butylene carbonate any one, also comprises in dimethyl carbonate, methyl ethyl carbonate and the diethyl carbonate any one.
Spendable lithium salts comprises and is selected from LiPF
6, LiBF
4, LiSbF
6, LiAsF
6, LiClO
4, LiCF
3SO
3, Li (CF
3SO
2)
2N, LiC
4F
9SO
3, LiAlO
4, LiAlCl
4, LiN (C
xF
2x+1SO
2) (C
yF
2y+1SO
2) (wherein x and y are natural number), the lithium salts of LiCl and LiI, and their mixture.It also comprises conventional lithium salts known in the chargeable lithium cell field.Preferably it comprises LiPF
6Or LiBF
4In any one.
Other suitable electrolyte comprises polymer such as ethylene oxide (PEO), propylene oxide (PPO), polyacrylonitrile (PAN), polyvinylidene fluoride (PVDF), polymethyl acrylate (PMA), polymethyl methacrylate (PMMA), and polymer impregnated polyelectrolyte in electrolyte organic solution.
Preferred CO
2Be dissolved in advance in the electrolyte organic solution (or electrolyte).Thus, CO
2Can form the lithium carbonate layer by reacting with some lithium ions that move to the negative pole position.The lithium carbonate layer compensates the reduction of the ionic conductivity that causes because of organic coating, therefore improves the cryogenic property of battery.
With the amount of 0.001~10% weight, more preferably the amount with 0.1~5% weight is added in the electrolyte preferred many acrylate compounds before being formed with organic coating.
The content of preferred many acrylate compounds is not less than 0.001% weight, because can not be formed with organic coating fully.If this content is greater than 10% weight, then organic coating is blocked up, and impedance increases inevitably.
With the amount of 0.001~10% weight, more preferably the amount with 0.05~1% weight is added in the electrolyte before being formed with organic coating for preferred acrylonitrile and/or methacrylonitrile.
The content of not preferred acrylonitrile and/or methacrylonitrile is less than 0.001% weight, because can not be formed with organic coating fully.If this content is greater than 10% weight, then organic coating is blocked up, and impedance increases inevitably.
Negative pole for example comprises by mixing the negative electrode active material powder with adhesive (as polyvinylidene fluoride) and the conductive agent of choosing wantonly (as carbon black) and make it to be configured as those negative poles that the roundel on plane prepares.The example of negative electrode active material is a carbonaceous material, as Delanium, native graphite, carbon fiber and graphite, the mesomorphic carbon of graphite (graphite meso carbon) microballon or amorphous carbon.Spendable negative electrode active material comprises can form the metal of alloy and the compound that comprises metal and carbonaceous material with lithium.Can comprise Al, Si, Sn, Pb, Zn, Bi, In, Mg, Ga and Cd with the metal that lithium forms alloy.In addition, also can use lithium metal foil as negative pole.
Should consider the form of organic coating on the negative terminal surface, and the coating state that is formed at the organic coating on the granular materials surface that constitutes negative electrode active material, perhaps be formed at the coating state of the organic coating on lithium metal foil surface.
Positive pole for example comprises by mixed cathode active material powder and adhesive (as polyvinylidene fluoride) and optional conductive agent (as carbon black) and makes it to be configured as sheet or circular those positive poles that prepare.The example of positive active material comprises lithium and at least a composite oxides that are selected from the metal of cobalt, manganese and nickel.Preferred LiMn
2O
4, LiCoO
2, LiNiO
2, LiFeO
2Perhaps V
2O
5It can also comprise the compound that can reversibly embed or deviate from lithium ion, as TiS, MoS, organic disulfide or organic polysulfide.
The illustrative methods of preparation chargeable lithium cell of the present invention hereinafter will be described.
Chargeable lithium cell comprises many acrylate compounds are added in the electrolyte, and gained electrolyte is placed between positive pole and the negative pole according to the assembly technology preparation.
Electrolyte can be polyelectrolyte or electrolyte organic solution.This method may further include before described interpolation step and prepares polyelectrolyte.At least a can the adding in acrylonitrile and the methacrylonitrile with many acrylate compounds.
The content of many acrylate compounds is preferably 0.01~10% weight, more preferably 0.1~5% weight.The content of acrylonitrile or methacrylonitrile is preferably 0.01~10% weight, more preferably 0.05~1% weight.
In this case, preferred CO
2Be dissolved in the electrolyte in advance.For with CO
2Be dissolved in the electrolyte, can adopt to blast CO
2Any method of gas.Because in advance with CO
2Be dissolved in electrolyte, move to some lithium ions and the CO of negative pole
2Reaction forms the lithium carbonate layer.The lithium carbonate layer has compensated the deterioration of the ionic conductivity of organic coating under the low temperature, so the cryogenic property of battery is improved.
Subsequently electrolyte is positioned between positive pole and the negative pole.When electrolyte is in liquid phase, its dipping be sealed in positive pole, the negative pole in the container and place positive pole and negative pole between dividing plate.And when electrolyte was solid phase or semi-solid phase, it inserted between positive pole and the negative pole.
Then, make comprise many acrylate compounds at least and place positive pole and negative pole between electrolyte stand 40~120 ℃ heating steps.In case heating electrolyte, then many acrylate compounds carry out radical polymerization and form polymer, and this polymer is immersed in the electrolyte organic solution.In addition, negative terminal surface is adsorbed some many acrylate compounds and/or acrylonitrile and/or methacrylonitrile.
Preferably do not heat under less than 40 ℃ temperature and carry out, because radical polymerization is carried out insufficiently, also not preferred temperature surpasses 120 ℃, because electrolyte generation sex change causes battery behavior to worsen.
In assembly technology, when electrolyte placed between positive pole and the negative pole, heating steps can omit.When adopting basically the electrolyte of forming by electrolyte organic solution, also can omit heating steps.
When acrylonitrile and/or methacrylonitrile are added in the electrolyte organic solution with many acrylate compounds, on negative pole, form the organic coating that comprises many acrylate compounds and acrylonitrile and/or methacrylonitrile.When comprising acrylonitrile and/or methacrylonitrile, organic coating has improved ionic conductivity and efficiency for charge-discharge, because internal resistance has reduced.Acrylonitrile and/or methacrylonitrile are formed with organic coating with the polymerization of many acrylate compounds.As selection, acrylonitrile and/or methacrylonitrile can be dissolved in the polymer of many acrylate compounds and be formed with organic coating.
In addition, in case be formed with organic coating, the many acrylate compounds in the electrolyte organic solution and the content of acrylonitrile and/or methacrylonitrile significantly reduce.
According to the method for preparing chargeable lithium cell, many acrylate compounds carry out radical polymerization by heating and form polymer, simultaneously, immerse this polymer by electrolyte organic solution and form polyelectrolyte.Thereby before the gained electrolyte decomposition, be formed with organic coating in negative terminal surface.
The following examples are used for setting forth in more detail the present invention, limit the scope of the present invention and can not be used as.
<utilize the electrolyte that includes only many acrylate compounds to prepare rechargeable lithium battary 〉
Embodiment 1
The electrolyte organic solution of trimethylolpropane triacrylate shown in the formula 1 of 0.2% weight (molecular weight is 269) and 99.8% weight was mixed 30 minutes, make electrolyte precursor.As for electrolyte organic solution, adopt 1M LiPF
6Ethylene carbonate and dimethyl carbonate (EC/DMC, volume ratio is 3: 7) solution.
Will be with LiCoO
2Placing with the carbon fiber for the sheet positive pole of positive active material is on the sheet negative pole of negative electrode active material, and they are inserted in the container, injects electrolyte then in container.With container encloses, obtain the Coin-shaped battery of 20 millimeters of diameters, 1.6 millimeters of thickness.
This Coin-shaped battery was heated 8 hours down at 40 ℃, obtain not have electric lithium battery.By heating battery, unreacted many acrylate compounds polymerization is formed with organic coating on negative pole.
Embodiment 2
Prepare chargeable lithium cell by the mode identical with embodiment 1, different is, (in formula 2, a+b+c=14) the electrolyte organic solution of the trimethylolpropane tris ethyoxyl triacrylate shown in (mean molecule quantity is 912) and 99.8% weight is mixed with the formula 2 of 0.2% weight.
Embodiment 3
Prepare chargeable lithium cell by the mode identical with embodiment 1, different is, (in formula 3, a+b+c=3) the electrolyte organic solution of the trimethylolpropane tris propoxyl group triacrylate shown in (mean molecule quantity is 460) and 99.8% weight is mixed with the formula 3 of 0.2% weight.
Embodiment 4
Prepare chargeable lithium cell by the mode identical with embodiment 1, different is, the dipentaerythritol acrylate of the caprolactone modification of 0.2% weight is mixed with the electrolyte organic solution of 99.8% weight.
<adopt to comprise that the electrolyte of many acrylate compounds and acrylonitrile or methacrylonitrile prepares rechargeable lithium battary
Embodiment 5
Prepare chargeable lithium cell by the mode identical with embodiment 1, different is, (in formula 1, a+b+c=14) methacrylonitrile of the trimethylolpropane tris ethyoxyl triacrylate shown in (mean molecule quantity is 405) and 0.1% weight mixes with the electrolyte organic solution of 99.8% weight with the formula 1 of 0.1% weight.
Embodiment 6
Prepare chargeable lithium cell by the mode identical with embodiment 1, different is, (in formula 2, a+b+c=14) methacrylonitrile of the trimethylolpropane tris ethyoxyl triacrylate shown in (mean molecule quantity is 912) and 0.1% weight mixes with the electrolyte organic solution of 99.8% weight with the formula 2 of 0.1% weight.
Embodiment 7
Prepare chargeable lithium cell by the mode identical with embodiment 1, different is, (in formula 3, a+b+c=3) acrylonitrile of the trimethylolpropane tris propoxyl group triacrylate shown in (mean molecule quantity is 460) and 0.1% weight mixes with the electrolyte organic solution of 99.8% weight with the formula 3 of 0.1% weight.
Embodiment 8
Prepare chargeable lithium cell by the mode identical with embodiment 1, different is, (in formula 3, a+b+c=3) acrylonitrile of the trimethylolpropane tris propoxyl group acrylate shown in (mean molecule quantity is 460) and 0.25% weight mixes with the electrolyte organic solution of 99.5% weight with the formula 3 of 0.25% weight.
Embodiment 9
Prepare chargeable lithium cell by the mode identical with embodiment 1, different is, (in formula 3, a+b+c=3) acrylonitrile of the trimethylolpropane tris propoxyl group triacrylate shown in (mean molecule quantity is 460) and 0.25% weight mixes with the electrolyte organic solution of 98.75% weight with the formula 3 of 1% weight.
Embodiment 10
Prepare chargeable lithium cell by the mode identical with embodiment 1, different is, the dipentaerythritol acrylate of the caprolactone modification of 0.1% weight and the acrylonitrile of 0.1% weight are mixed with the electrolyte organic solution of 99.8% weight.
Comparative Examples 1
Prepare chargeable lithium cell by the mode identical with embodiment 1, different is not use the trimethylolpropane triacrylate shown in the formula 1 (mean molecule quantity is 269).
The reserve capacity of<embodiment 1~10 and Comparative Examples 1 〉
The chargeable lithium cell of embodiment 1~10 and Comparative Examples 1 is discharged and recharged 50 times, and measure first capacitance and the 50th discharge capacity of visiting.
According to the 50th discharge capacity ratio to first discharge capacity, calculated capacity keeps percentage.The results are shown in the following table 1.
Table 1
Capacity keeps percentage | |
Embodiment 1 | 100 |
Embodiment 2 | 88 |
Embodiment 3 | 86 |
Embodiment 4 | 100 |
Embodiment 5 | 80 |
Embodiment 6 | 75 |
Embodiment 7 | 100 |
Embodiment 8 | 89 |
Embodiment 9 | 72 |
Embodiment 10 | 88 |
Comparative Examples 1 | 55 |
Table 1 clearly illustrates that the battery that has wherein added the embodiment 1~10 of many acrylate compounds has greater than 70% reserve capacity, and is better than the reserve capacity of the battery of Comparative Examples 1.
Embodiment 11
The dipentaerythritol acrylate of the caprolactone modification of 0.2% weight was mixed 30 minutes with the electrolyte organic solution of 99.8% weight, make electrolyte precursor.As for electrolyte organic solution, adopt 1M LiPF
6Ethylene carbonate and dimethyl carbonate (EC/DMC, volume ratio is 3: 7) solution.
Will be with LiCoO
2Being stacked on the carbon fiber for the sheet positive pole of positive active material is on the sheet negative pole of negative electrode active material, and they are bent to oval-shaped jelly web-like, is inserted in the rectangular tank.Encapsulate this container, obtain the prismatic lithium battery of 4 millimeters of thickness, 3 millimeters of width, 60 millimeters of height.
Comparative Examples 2
Prepare two prismatic lithium batteries by the mode identical with embodiment 11, different is not use the dipentaerythritol acrylate of caprolactone modification.
<keep about the initial discharge capacity of embodiment 11 and Comparative Examples 2
With the speed that discharges and recharges of 0.2C, make it activation for twice by four battery charging and dischargings to embodiment 11 (two batteries: be numbered 1 and 2) and Comparative Examples 2 (two batteries: be numbered 1 and 2).Then they are charged under 0.5C, and under the speed of 0.2C, 0.5C, 1C and 2C, discharge, and measure its discharge capacity under each speed.The results are shown in Table 2.
Table 2
The velocity of discharge (C) | Discharge capacity (nAh) | |
Embodiment 11 (1) | 2 | 584 |
1 | 645 | |
0.5 | 655 | |
0.2 | 662 | |
Embodiment 11 (2) | 2 | 586 |
1 | 647 | |
0.5 | 654 | |
0.2 | 661 | |
Comparative Examples 2 (1) | 2 | 549 |
1 | 634 | |
0.5 | 643 | |
0.2 | 649 | |
Comparative Examples 2 (2) | 2 | 555 |
1 | 632 | |
0.5 | 642 | |
0.2 | 649 |
As shown in table 2, to compare with the battery of Comparative Examples 2, the battery of embodiment 11 has discharge capacity and initial discharge capacity preferably, and this shows that adding many acrylate compounds can improve discharge capacity.
By inference, owing to the organic coating of the battery of embodiment 11 having been used the many acrylate compounds that prevent that negative pole and electrolyte from reacting, thus the electrolyte consistency, and efficiency for charge-discharge improves.
The cycle life characteristics of the chargeable lithium cell of<embodiment 11 and Comparative Examples 2 〉
Fig. 1 shows the period of chargeable lithium cell of embodiment 11 and Comparative Examples 2 and the relation between the discharge capacity, and this is to measure when they charge with the charging rate of 0.5C and discharge with the velocity of discharge of 1C.
As shown in Figure 1, the discharge capacity of the battery of the embodiment 11 that records after 50 circulations is a little more than Comparative Examples 2.If along with charge and discharge cycles come the comparison discharge capacity, then can make discharge capacity because of adding the judgement that many acrylate compounds are improved.
This is because formed many acrylate organic coating on the negative terminal surface of embodiment 11, thereby can prevent the decomposition of electrolyte, prevents the sex change of electrolyte, and improves efficiency for charge-discharge.
And in Comparative Examples 2, because negative pole contacts with the direct of electrolyte, electrolyte sex change and efficiency for charge-discharge reduce along with the increase of circulation.
Embodiment 12
Trimethylolpropane triacrylate shown in the formula 1 of 0.2% weight (molecular weight is 269) was mixed 30 minutes with the electrolyte organic solution of 99.8% weight.To wherein blasting CO
2Gas makes electrolyte precursor.As for electrolyte organic solution, adopt 1M LiPF
6Ethylene carbonate, diethyl carbonate and gamma-butyrolacton (EC/DEC/GBL, volume ratio is 1: 1: 1) solution.
Will be with LiCoO
2Being stacked on the carbon fiber for the sheet positive pole of positive active material is on the sheet negative pole of negative electrode active material, and they are bent to oval-shaped jelly web-like, is inserted in the rectangular tank.Encapsulate this container, obtain the prismatic lithium battery of 4 millimeters of thickness, 30 millimeters of width, 60 millimeters of height.
The gained prismatic batteries was heated 3 hours down at 60 ℃.
Comparative Examples 3
Prepare the prismatic lithium battery by the mode identical with embodiment 12, different is not use trimethylolpropane triacrylate.
The cycle life characteristics of the chargeable lithium cell of<embodiment 12 and Comparative Examples 3 〉
Fig. 2 shows the period of prismatic lithium battery of embodiment 12 and Comparative Examples 3 and the relation between the discharge capacity, and this is to measure when they charge with the charging rate of 0.5C and discharge with the velocity of discharge of 1C.
In addition, table 3 has provided under the room temperature with respect to first discharge capacity (600mAh) embodiment 12 and the Comparative Examples 3 discharge reservation amount at the 50th time and the 100th time circulation time.Discharge capacity when it gives battery and discharges and recharges under-20 ℃.
Table 3
When capacitance reservation amount (%, room temperature) | Discharge capacity (mAh ,-20 ℃) | ||
The 50th circulation | The 100th circulation | ||
Embodiment 12 | 93.7 | 81.7 | 521 |
Comparative Examples 3 | 71.6 | 28.7 | 515 |
Shown in Fig. 2 and table 3, proceed to 100 circulation times, the discharge capacity of the battery of embodiment 12 is apparently higher than the discharge capacity of the battery of Comparative Examples 3.When the solvent of electrolyte organic solution comprised GBL, discharge capacity was improved by adding many acrylate compounds.
And in Comparative Examples 3, owing to negative pole contacts with the direct of electrolyte, thus the electrolyte sex change, and efficiency for charge-discharge reduces along with repeating of circulation.
As shown in table 3, to compare with the battery of Comparative Examples 3, the battery of embodiment 12 charge/discharge capacity at low temperatures is because many acrylate compounds and CO
2Adding and be improved.It is believed that these improvement are because many acrylate compounds and CO
2Adding cause.
As mentioned above, many acrylate compounds are at first polymerization when primary charging, is formed with organic coating in negative terminal surface, therefore, also can prevent electrolyte decomposition even charging voltage raises.Like this, the gas that produces because of electrolyte decomposition descends, and the sex change of electrolyte reduces.Therefore, in the chargeable lithium cell that is provided, charge/discharge capacity does not reduce, but cycle life characteristics has improved.
Although the present invention is had been described in detail with reference to preferred embodiment, but those skilled in the art is to be understood that, under the situation of design of the present invention that does not break away from the appended claims to be set forth and scope, can make various modifications or replacement to the present invention.
Claims (16)
1. rechargeable lithium battary comprises:
Can embed and deviate from the positive pole of lithium;
Can embed and deviate from the negative pole of lithium; With
Electrolyte,
Wherein this electrolyte comprises the many acrylate compounds with three or more acrylic acid groups of 0.001~1% weight, and at least a in acrylonitrile and the methacrylonitrile.
2. according to the chargeable lithium cell of claim 1, wherein this electrolyte comprises at least a in the acrylonitrile of 0.001~10% weight and the methacrylonitrile.
3. according to the chargeable lithium cell of claim 2, wherein this electrolyte comprises at least a in the acrylonitrile of 0.005~1% weight and the methacrylonitrile.
5. according to the chargeable lithium cell of claim 1, wherein these many acrylate compounds have the dipentaerythritol structure.
6. according to the chargeable lithium cell of claim 1, wherein these many acrylate compounds have six acrylic acid groups.
7. according to the chargeable lithium cell of claim 1, wherein this electrolyte further comprises CO
2
8. rechargeable lithium battary comprises:
Anodal;
Negative pole; With
The electrolyte that comprises electrolyte organic solution, this electrolyte comprise the many acrylate with three or more acrylic acid groups of 0.001~1% weight,
Wherein this negative terminal surface has been coated with and has comprised at least a organic layer in many acrylate compounds and acrylonitrile and the methacrylonitrile.
10. chargeable lithium cell according to Claim 8, wherein these many acrylate compounds have the dipentaerythritol structure.
11. chargeable lithium cell according to Claim 8, wherein these many acrylate compounds have six acrylic acid groups.
12. chargeable lithium cell according to Claim 8, wherein this electrolyte further comprises CO
2
13. a method for preparing rechargeable lithium battary comprises:
Many acrylate compounds with three or more acrylic acid groups of 0.001~1% weight are added in the electrolyte, and when adding many acrylate compounds, further in electrolyte, add at least a in acrylonitrile and the methacrylonitrile; And
This electrolyte is placed between positive pole and the negative pole, and wherein said positive pole and negative pole can embed and deviate from lithium.
14., further be included in the step that 40~120 ℃ temperature range heats this electrolyte according to the method for claim 13.
15., wherein in this electrolyte, add at least a in the acrylonitrile of 0.01~10% weight and the methacrylonitrile according to the method for claim 13.
16. the method according to claim 13 further comprises CO
2Be dissolved in this electrolyte.
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KR100529085B1 (en) * | 2003-09-24 | 2005-11-15 | 삼성에스디아이 주식회사 | Electrolyte for lithium secondary battery and lithium secondary battery fabricated using same |
KR100866764B1 (en) | 2006-09-25 | 2008-11-03 | 주식회사 엘지화학 | Non-aqueous electrolyte and electrochemical device comprising the same |
CN103038930B (en) * | 2010-07-28 | 2017-12-05 | 株式会社Lg化学 | Secondary lithium batteries nonaqueous electrolyte and the lithium secondary battery for including it |
KR101545432B1 (en) * | 2013-01-28 | 2015-08-18 | 주식회사 엘지화학 | Lithium secondary battery |
EP2790260B1 (en) | 2013-01-28 | 2016-03-23 | LG Chem, Ltd. | Composition for gel polymer electrolyte and lithium secondary battery comprising same |
WO2014116085A1 (en) | 2013-01-28 | 2014-07-31 | 주식회사 엘지화학 | Lithium secondary battery |
TWI760922B (en) * | 2020-11-17 | 2022-04-11 | 國立成功大學 | Electrolyte and fabricating method thereof, and lithium battery |
CN114552026B (en) * | 2021-03-30 | 2023-08-25 | 天津力神电池股份有限公司 | Lithium battery adopting targeted in-situ polyelectrolyte and preparation method thereof |
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CN1317512A (en) * | 2001-05-25 | 2001-10-17 | 复旦大学 | Process for preparing gel-state lithium ion polymer as electrolyte and bettery |
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