JP2014229563A - Method for manufacturing power storage device - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a manufacturing method which allows a power storage device to be manufactured in a short length of time while preventing Li deposition and an undesired reaction on a negative electrode.SOLUTION: A method for manufacturing a power storage device having a positive electrode, a negative electrode including at least SiO(0<x<2), and an electrolyte containing an additive agent for forming a film on SiOat a decomposition potential of 1.7 V(vsLi/Li) or below comprises: a first charging step of charging the power storage device at a first temperature at least until the potential of the negative electrode reaches the decomposition potential; and a second charging step of charging the power storage device at a second temperature higher than the first temperature at least for a predetermined period of time after the potential of the negative electrode reaches the decomposition potential.

Description

  The present invention relates to a method for manufacturing a power storage device.

  Lithium-ion secondary batteries are lightweight and have high capacity, so they are widely applied as power sources for portable electronic devices, etc., and have recently been listed as promising candidates for power sources mounted in hybrid vehicles and electric vehicles. Yes.

As the negative electrode active material of the lithium ion secondary battery, a material that is alloyed with lithium is used from the viewpoint of increasing the capacity of the battery. Among such materials, in particular, SiO _x (0 <x <2) having a larger theoretical capacity than that of conventionally used carbon materials is expected (Patent Documents 1 to 3).

JP 2011-249046 A JP 2011-065841 A JP 2012-209195 A

By the way, from the viewpoint of production efficiency, it is desired to shorten the time required for battery production. However, since the above-mentioned SiO _x contains high-resistance SiO ₂ as a component, there is a problem that when initial charging is performed at a high rate, the negative electrode potential becomes 0 V or less due to a voltage drop and Li is deposited. In order to avoid this problem, when the initial charge is performed at a high temperature, the resistance of the electrolytic solution is lowered, so that Li does not easily precipitate even when charged at a high rate, but it is not preferable such as a decomposition reaction of a solvent on the negative electrode. Reaction occurs. Such a reaction leads to swelling of the battery or contamination of the electrolyte, etc., so that the battery itself deteriorates. Therefore, in a battery using SiO _x as a negative electrode active material, the initial charge must be performed at a low rate at a low temperature.

  The present invention has been made in view of the above-described problems, and an object of the present invention is to provide a manufacturing method capable of manufacturing a power storage device in a short time while preventing Li precipitation and an undesirable reaction on the negative electrode. And

The present invention relates to an electrolysis comprising a positive electrode, a negative electrode containing at least SiO _x (0 <x <2), and an additive that forms a film on SiO _x at a decomposition potential of 1.7 V (vsLi / Li ⁺ ) or less. And a liquid storage device comprising the liquid. The method includes a first charging step of charging the power storage device at a first temperature at least until the potential of the negative electrode reaches the decomposition potential, and the power storage device for at least a predetermined period after the potential of the negative electrode reaches the decomposition potential. And a second charging step of performing further charging at a second temperature higher than the first temperature.

According to such a manufacturing method, first, in the first charging step, a film called SEI (Solid Electrode Interface) is formed on the negative electrode active material. In the first charging step, since the power storage device is not heated, an undesirable reaction such as a decomposition reaction of a solvent on the negative electrode active material before film formation is suppressed. On the other hand, in the second charging step, by heating, reaction resistance such as Li movement resistance in the electrolytic solution and Li intercalation in SiO _x is lowered. Therefore, it becomes possible to charge at high speed while suppressing the precipitation of Li. In addition, after a film called SEI is formed on the surface of the negative electrode active material, even when the power storage device is heated, undesirable reactions such as a decomposition reaction of the solvent hardly occur and the battery can be charged at a high rate. It becomes like this. Therefore, the time required for manufacturing the power storage device can be shortened.

  In the said manufacturing method, it is preferable that 1st temperature is 15-30 degreeC. Thereby, the undesirable reaction on the negative electrode in the first charging step can be more effectively prevented.

  In the said manufacturing method, it is preferable that 2nd temperature is 30-60 degreeC. Thereby, even if it charges with a higher rate in a 2nd charge process, since it becomes difficult to precipitate Li, the time which initial charge requires can be shortened more.

  The additive preferably contains an oxalato complex. When the oxalato complex reacts on the negative electrode, the reaction proceeds while the oxalato complexes are polymerized, so that a stronger SEI film tends to be formed. More preferably, the oxalato complex contains lithium bisoxalatoborate (LiBOB).

  In the above manufacturing method, the power storage device is preferably a lithium ion secondary battery.

  ADVANTAGE OF THE INVENTION According to this invention, the manufacturing method which can manufacture an electrical storage apparatus in a short time can be provided, preventing the precipitation of Li and the undesirable reaction on a negative electrode.

FIG. 1 is a schematic cross-sectional view of a lithium ion secondary battery according to an embodiment of the present invention. FIG. 2 is a potential profile of the positive electrode and the negative electrode in the initial charge of the lithium ion secondary battery according to the embodiment of the present invention.

  Hereinafter, an example of an embodiment according to the present invention will be described with reference to the drawings.

(Power storage device)
Hereinafter, a lithium ion secondary battery which is one of the power storage devices according to this embodiment will be described as an example. FIG. 1 is a schematic cross-sectional view of a lithium ion secondary battery according to this embodiment. As shown in FIG. 1, the lithium ion secondary battery 100 mainly includes a positive electrode 10, a separator 20, a negative electrode 30, a case 70, and an electrolytic solution.

(Positive electrode)
The positive electrode 10 includes a positive electrode current collector 12 and a positive electrode active material layer 14 provided on the positive electrode current collector 12. The positive electrode active material layer 14 refers to a region where the active material is applied in the positive electrode current collector 12. As shown in FIG. 1, the positive electrode active material layer 14 may be provided only on one surface of the positive electrode current collector 12, or may be provided on both surfaces of the positive electrode current collector 12.

  The positive electrode current collector 12 is made of a conductive material. Examples of the material of the positive electrode current collector 12 are metal materials such as stainless steel, titanium, nickel, aluminum, and copper, or conductive resins. In particular, aluminum is suitable as a material for the positive electrode current collector 12. Although the thickness of the positive electrode current collector 12 is not particularly limited, for example, the positive electrode current collector 12 can have a foil shape (15 to 20 μm).

The positive electrode active material layer 14 includes a positive electrode active material and a binder. An example of the positive electrode active material is a composite oxide containing Li and at least one element selected from the group consisting of lithium oxide, Ni, Mn, and Co. Examples of the composite oxide include lithium cobalt composite oxide LiCoO ₂ , lithium nickel composite oxide LiNiO ₂ , lithium manganese composite oxide LiMnO ₂ , LiMn ₂ O ₄ , lithium nickel cobalt composite oxide LiNi _a Co _b O ₂ ( a + b = 1,0 <a < 1,0 <b <1), lithium-manganese-cobalt composite oxide _{LiMn a Co b O 2 (a} + b = 1,0 <a <1,0 <b <1), lithium cobalt nickel manganese composite oxide _{LiCo p Ni q Mn r O 2} (p + q + r = 1,0 <p <1,0 <q <1,0 <r <1).

  The binder fixes the active material to the current collector. Examples of the binder are fluorine-containing resins such as polyvinylidene fluoride, polytetrafluoroethylene, and fluororubber, thermoplastic resins such as polypropylene and polyethylene, imide resins such as polyimide and polyamideimide, and alkoxysilyl group-containing resins. The quantity of a binder can be 1-30 mass parts with respect to 100 mass parts of active materials.

  The positive electrode active material layer 14 can further contain a conductive additive as necessary. Examples of the conductive aid are carbon-based particles such as carbon black, graphite, acetylene black (AB), ketjen black (registered trademark) (KB), vapor grown carbon fiber (VGCF). These can be added alone or in combination of two or more. Although it does not specifically limit about the usage-amount of a conductive support agent, For example, it can be set as 1-30 mass parts with respect to 100 mass parts active material.

  The positive electrode current collector 12 has a tab portion 12t at the end thereof where the positive electrode active material layer 14 is not formed. A lead 16 described later is electrically connected to the tab portion 12t.

(Negative electrode)
The negative electrode 30 includes a negative electrode current collector 32 and a negative electrode active material layer 34 provided on the negative electrode current collector 32. The negative electrode active material layer 34 refers to a region of the negative electrode current collector 32 where the negative electrode active material is applied. The negative electrode current collector 32 is made of a conductive material. Examples of the material of the negative electrode current collector 32 include those exemplified as the material of the positive electrode current collector 12 described above, and copper is particularly preferable. The negative electrode current collector 32 can be formed in a foil shape like the positive electrode current collector 12.

  The negative electrode active material layer 34 has a negative electrode active material and a binder. The negative electrode active material layer 34 may contain a conductive additive as necessary. Examples and blending amounts of the binder and the conductive auxiliary agent can be the same as those described for the positive electrode 10.

In the present embodiment, the negative electrode active material is SiO _x (0 <x <2). SiO _x has a Si phase and a SiO ₂ phase in each particle. The Si phase is very fine and is dispersed in the SiO ₂ phase. Further, the SiO ₂ phase covering the Si phase has a function of suppressing decomposition of the electrolytic solution.
Here, when x is less than 0.5, the proportion of the Si phase increases, so that the volume change during charge / discharge becomes too large, and the cycle characteristics tend to be difficult to improve. Moreover, when x exceeds 1.5, the ratio of Si phase may fall and energy density may fall. Therefore, x is preferably 0.5 to 1.5, and more preferably 0.7 to 1.2.

Such SiO _x can be obtained by disproportionating SiO, which is an amorphous silicon oxide obtained using silicon dioxide (SiO ₂ ) and simple silicon (Si) as raw materials, by heat treatment or the like. The disproportionation reaction is a reaction in which SiO is decomposed into a Si phase and a SiO ₂ phase. In general, when oxygen is turned off, it is said that almost all SiO is disproportionated and separated into two phases at 800 ° C. or higher. Specifically, non-crystalline SiO powder is subjected to heat treatment at 800 to 1200 ° C. for 1 to 5 hours in an inert atmosphere such as in a vacuum or in an inert gas. SiO _x containing two phases, a _two- phase and a crystalline Si phase, is obtained.

  The particle size D50 of the silicon oxide powder is preferably 4 μm or more. The particle diameter D50 is a median diameter, and can be obtained based on a volume-based particle size distribution by a laser diffraction method. The particle size D50 of the silicon oxide powder is preferably 20 μm or less, and preferably 15 μm or less.

The negative electrode current collector 32 has a tab portion 32t at the end thereof where the negative electrode active material layer 34 is not formed. A lead 36 described later is electrically connected to the tab portion 32t. The negative electrode can also contain a negative electrode active material other than SiO _x .

(Separator)
The separator 20 separates the positive electrode 10 and the negative electrode 30 and allows lithium ions to pass through while preventing a short circuit of current due to contact between both electrodes. As the separator 20, for example, a porous film made of a synthetic resin such as polytetrafluoroethylene, polypropylene, or polyethylene, or a porous film made of ceramics can be used. The positive electrode active material layer 14 of the positive electrode 10 and the negative electrode active material layer 34 of the negative electrode 30 are in contact with each surface of the separator 20.

(Electrolyte)
The electrolytic solution includes an electrolyte and a solvent that dissolves the electrolyte. The electrolyte is impregnated in the positive electrode active material layer 14, the separator 20, and the negative electrode active material layer 34.

Examples of the electrolyte are lithium salts such as LiBF ₄ , LiPF ₆ , LiClO ₄ , LiAsF ₆ , LiCF ₃ SO ₃ , and LiN (CF ₃ SO ₂ ) ₂ . These lithium salts may be used alone or in combination of two or more.

  Examples of the solvent are cyclic esters, chain esters, and ethers. Two or more of these solvents can be mixed. Examples of cyclic esters are ethylene carbonate, propylene carbonate, butylene carbonate, gamma butyrolactone, vinylene carbonate, 2-methyl-gamma butyrolactone, acetyl-gamma butyrolactone, gamma valerolactone. Examples of chain esters are dimethyl carbonate, diethyl carbonate, dibutyl carbonate, dipropyl carbonate, ethyl methyl carbonate, propionic acid alkyl ester, malonic acid dialkyl ester, and acetic acid alkyl ester. Examples of ethers are tetrahydrofuran, 2-methyltetrahydrofuran, 1,4-dioxane, 1,2-dimethoxyethane, 1,2-diethoxyethane, 1,2-dibutoxyethane.

  The density | concentration of the electrolyte in electrolyte solution can be 0.5-1.7 mol / L, for example. The electrolytic solution may contain a gelling agent.

The electrolytic solution of this embodiment further has an additive that forms a film called SEI on a negative electrode active material such as SiO _x at a decomposition potential Vr of 1.7 V or less. Note that the electrode potential in this specification is the potential with respect to Li / Li ⁺ for both the positive electrode and the negative electrode.

  As such an additive, an oxalato complex is preferable. The oxalato complex easily forms a strong film on the negative electrode active material by the polymerization reaction of the oxalato part of the additive with the oxalate part of the other additive on the surface of the negative electrode active material. As the oxalato complex, a complex whose central element is boron or phosphorus is particularly preferable. Further, when the central element is phosphorus, it is more preferable that the complex contains halogen. Examples of such oxalato complexes include lithium bisoxalatoborate (LiBOB: Vr = 1.8 V) represented by the following chemical formula (1) and lithium oxalatophosphates represented by the following general formula (2). Is mentioned. These additives may be used alone or in combination of two or more.

  Moreover, the compound which the organic group which carries out an ester bond with a carbonate group has a double bond as said additive can also be used. Examples of such compounds include vinylene carbonate (Vr = 1.35V) and vinylene carbonate derivatives.

  The concentration of the additive in the electrolytic solution can be, for example, 0.01 to 0.2 mol / L.

(Case)
The case 70 accommodates the positive electrode 10, the separator 20, the negative electrode 30, and the electrolytic solution. The material and form of the case are not particularly limited, and various known materials such as resins and metals can be used.

  Leads 16 and 36 are connected to the tab portion 12t of the positive electrode current collector 12 and the tab portion 32t of the negative electrode current collector 32, respectively. One ends of the leads 16 and 36 are out of the case 70.

(Method for manufacturing power storage device)
Next, a method for manufacturing the power storage device according to this embodiment will be described with reference to the drawings as necessary.

  The above-described positive electrode 10, separator 20, negative electrode 30, case 70, and lithium ion secondary battery 100 mainly including an electrolytic solution are prepared. Next, the lithium ion secondary battery 100 is initially charged.

FIG. 2 is an example of potential profiles of the positive electrode and the negative electrode in the initial charge of the lithium ion secondary battery according to the embodiment of the present invention. In FIG. 2, a curve 41 represents the positive electrode potential, and a curve 42 represents the negative electrode potential. In the production method of this embodiment, first, in the first charging step T _1, until the potential of at least the negative electrode reaches the decomposition potential Vr of the additive, to charge the lithium ion secondary cell 100 at a first temperature. Here, the first temperature is the temperature of the battery in the first charging step T _1, preferably a 15 to 30 ° C.. First charging step _{T 1,} for example, it can be performed at a charge rate of 0.02C～0.5C.

As charging progresses, the potential of the negative electrode decreases, and the potential of the negative electrode reaches a potential Vr at which the decomposition reaction of the additive contained in the electrolytic solution occurs. As described above, in this embodiment, Vr is 1.7V or less. When the potential of the negative electrode reaches the decomposition potential Vr of the additive, a film called SEI is formed on the negative electrode active material such as SiO _x .

Potential of the negative electrode after reaching the decomposition potential Vr of the additive, at a predetermined timing, to start the heating of the lithium ion secondary battery 100, the process proceeds to the second charging step T _2. Here, the battery is further charged for at least a predetermined period after reaching the decomposition potential Vr of the additive at the second temperature, which is higher than the first temperature. A method for heating the lithium ion secondary battery 100 is not particularly limited, and for example, a method of heating using a heater or a thermostatic bath can be used. Here, the second temperature is preferably 30 to 60 ° C.

In the second charging step T _2, since it is formed films already called SEI on the anode active material, hardly occur undesirable reactions such as decomposition reaction of the solvent on the anode active material, charging at a high rate be able to. The charge rate is, for example, 0.1C to 1.0C. Since charging can be performed at a high rate in this way, the time required for initial charging can be shortened. After the voltage between the positive and negative electrodes reaches a predetermined voltage, for example, 4.2 V, the constant current charging can be changed to the constant voltage charging.

Transitioning from the first charging step T ₁ to the second charging step T _2, i.e., the timing of starting the heating, after the negative electrode potential has reached the Vr, ie, it may be anytime less than the negative electrode potential Vr, It is preferable to start heating when the negative electrode potential is Vr-1.0 V or more. It is preferable to start charging at the above timing because it is possible to prevent the potential of the negative electrode from being lowered too much before starting heating and to start charging at a high rate early.

  In addition, the lithium ion secondary battery 100 according to the present embodiment is not limited to the above embodiment, and various modifications are possible. For example, a plurality of positive electrodes, negative electrodes, and separators may be provided, the positive electrodes and the negative electrodes may be alternately disposed, and the separators may be disposed between the positive electrodes and the negative electrodes. Further, the positive electrode and the negative electrode may be wound so that a separator is interposed between them.

Moreover, the negative electrode 30 in the lithium ion secondary battery 100 according to the present embodiment may be one in which the irreversible capacity of SiO _x contained in the negative electrode active material is reduced in advance before the initial charge. As a method of reducing the irreversible capacity of SiO _x , powder or foil-like metal Li and SiO _x are contacted in a dry or wet manner, and an intercalation reaction between the metal Li and SiO _x is performed on SiO _x . Examples include a method of pre-doping Li. Further, in the intercalation reaction, aging may be performed at a high temperature in order to proceed the reaction uniformly.

  Furthermore, although the lithium ion secondary battery was illustrated in the said embodiment, it is applicable also to electrical storage apparatuses, such as a lithium ion capacitor, for example.

DESCRIPTION OF SYMBOLS 10 ... Positive electrode, 30 ... Negative electrode, 12, 32 ... Current collector, 12t, 32t ... Tab part, 14 ... Positive electrode active material layer, 34 ... Negative electrode active material layer, 20 ... Separator, 16, 36 ... Lead, 70 ... Case , 100: lithium ion secondary battery, 41: positive electrode potential, 42: negative electrode potential.

Claims (6)

A positive electrode;
A negative electrode containing at least SiO _x (0 <x <2);
An electrolyte containing an additive that forms a film on SiO _x at a decomposition potential of 1.7 V (vsLi / Li ⁺ ) or less;
A method of manufacturing a power storage device comprising:
A first charging step of charging the power storage device at a first temperature until at least the potential of the negative electrode reaches the decomposition potential;
A second charging step of further charging the power storage device at a second temperature higher than the first temperature in at least a predetermined period after the potential of the negative electrode reaches the decomposition potential;
A manufacturing method comprising:   The manufacturing method of the electrical storage apparatus of Claim 1 whose said 1st temperature is 15-30 degreeC.   The manufacturing method of the electrical storage apparatus of Claim 1 or 2 whose said 2nd temperature is 30-60 degreeC.   The manufacturing method of the electrical storage apparatus of any one of Claims 1-3 in which the said additive contains an oxalato complex.   The method for manufacturing a power storage device according to claim 4, wherein the oxalato complex includes lithium bisoxalatoborate (LiBOB).   The method for manufacturing a power storage device according to claim 1, wherein the power storage device is a lithium ion secondary battery.

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