JP7249885B2 - All solid state lithium ion secondary battery system and device and method for charging all solid state lithium ion secondary battery - Google Patents

Description

The present invention relates to an all-solid-state lithium-ion secondary battery system, and an apparatus and method for charging an all-solid-state lithium-ion secondary battery.

In recent years, in order to cope with global warming, reduction of the amount of carbon dioxide is earnestly desired. In the automobile industry, expectations are gathering for the reduction of carbon dioxide emissions through the introduction of electric vehicles (EV) and hybrid electric vehicles (HEV). Development of electrolyte secondary batteries has been actively carried out.

Secondary batteries for motor driving are required to have extremely high output characteristics and high energy compared to consumer lithium-ion secondary batteries used in mobile phones, notebook computers, and the like. Therefore, lithium-ion secondary batteries, which have the highest theoretical energy among all practical batteries, have attracted attention and are being rapidly developed.

Lithium ion secondary batteries, which are currently in widespread use, use a combustible organic electrolyte as an electrolyte. Such a liquid type lithium ion secondary battery requires stricter safety measures against liquid leakage, short circuit, overcharge, etc. than other batteries.

Therefore, in recent years, research and development on all-solid-state lithium-ion secondary batteries using oxide-based or sulfide-based solid electrolytes have been actively carried out. A solid electrolyte is a material composed mainly of an ionic conductor capable of conducting ions in a solid. Therefore, in all-solid-state lithium ion secondary batteries, in principle, various problems due to combustible organic electrolytes do not occur unlike conventional liquid-type lithium ion secondary batteries. In general, the use of a high-potential, large-capacity positive electrode material and a large-capacity negative electrode material can significantly improve the output density and energy density of the battery. A promising candidate is an all-solid-state lithium-ion secondary battery that uses a sulfide-based material as a positive electrode active material and metallic lithium or a lithium-containing alloy as a negative electrode active material.

By the way, in a lithium ion secondary battery, the negative electrode potential decreases as the charging progresses. When the negative electrode potential drops below 0 V (vs. Li/Li ⁺ ), metallic lithium precipitates on the negative electrode and dendrite (dendritic) crystals precipitate (this phenomenon is also referred to as metallic lithium electrodeposition). When the electrodeposition of metallic lithium occurs, there is a problem that the deposited dendrite penetrates the electrolyte layer and causes an internal short circuit of the battery. Moreover, in the liquid type lithium ion secondary battery, there is also a problem that the organic electrolytic solution constituting the electrolyte is reductively decomposed by reacting with highly active dendrites.

Here, in an all-solid battery using a sulfide solid electrolyte (sulfide all-solid battery), internal resistance may increase when used in a heated state. When a sulfide all-solid-state battery with increased internal resistance is rapidly charged, the reaction tends to concentrate on the active material on the surface of the negative electrode active material layer, and the potential on the surface of the negative electrode active material layer decreases, resulting in the electrodeposition of metallic lithium. may occur.

As a means for solving such problems, Patent Document 1 discloses an all-solid-state battery using a sulfide solid electrolyte containing Li, P and S and having PS ₄ ^3- as a main skeleton. A first output unit that outputs a heating signal for heating above, a second output unit that outputs a charging signal for charging the heated all-solid-state battery based on the heating signal, and a control that controls the heating signal A charging control device for a sulfide all-solid-state battery is disclosed. According to Patent Document 1, since the resistance of the sulfide all-solid-state battery as described above does not easily increase even if the temperature is raised to 60 ° C. or higher, the electrodeposition of metallic lithium can be achieved by charging at an elevated temperature. It is stated that it is possible to prevent the occurrence of such as, and that it is also compatible with quick charging.

JP 2014-86209 A

Here, the sulfide all-solid-state battery disclosed in Patent Document 1 is based on the assumption that an active material capable of intercalating and deintercalating lithium ions, such as graphite, is used as the negative electrode active material instead of metal lithium or a lithium-containing alloy. be. In such a negative electrode active material, electrodeposited metallic lithium becomes irreversible, resulting in a decrease in battery capacity. Therefore, in Patent Document 1, the charging process is stopped when it is determined that electrodeposition has occurred based on a rapid drop in battery voltage during charging.

On the other hand, negative electrode active materials such as metallic lithium and lithium-containing alloys have large capacities and are advantageous in significantly improving the output density and energy density of batteries. It is synonymous with the generation of analysis. Therefore, in an all-solid-state battery using metallic lithium or a lithium-containing alloy as the negative electrode active material, it is necessary to control the charging process so that the charging process can be continued without problems even if electrodeposition occurs, while presupposing the occurrence of electrodeposition. be. If the charging process can be continued even if electrodeposition occurs in this way, the large capacity of these negative electrode active materials can be fully utilized, contributing to a significant improvement in the output density and energy density of the battery. be able to.

Therefore, in an all-solid-state battery using metallic lithium or a lithium-containing alloy as a negative electrode active material, on the premise that metallic lithium is electrodeposited, a means for continuing the charging process even if electrodeposition occurs is provided. intended to provide

The present inventors have made intensive studies to solve the above problems. As a result, when charging an all-solid-state lithium-ion secondary battery using metallic lithium or a lithium-containing alloy as a negative electrode active material, the strain energy generated in the solid electrolyte layer due to charging of the battery increases the strain energy of the solid electrolyte layer. The above problem can be solved by calculating the threshold temperature from the temperature at which the crack growth energy calculated from the fracture toughness value becomes smaller, and controlling the temperature of the battery so as to exceed the calculated threshold temperature. and completed the present invention.

An all-solid-state lithium-ion secondary battery system according to one embodiment of the present invention includes, first, a positive electrode containing a positive electrode active material layer containing a positive electrode active material, and a negative electrode active material containing a negative electrode active material containing metallic lithium or a lithium-containing alloy. An all-solid-state lithium-ion secondary battery including a power generation element having a negative electrode including a material layer and a solid electrolyte layer interposed between the positive electrode active material layer and the negative electrode active material layer. Further, the system includes a charger for charging the all-solid-state lithium ion secondary battery, a temperature detection unit for detecting the temperature of the all-solid-state lithium-ion secondary battery, and the temperature of the all-solid-state lithium ion secondary battery. and a control unit for controlling the temperature of the all-solid-state lithium ion secondary battery. Then, when the charger charges the all-solid-state lithium-ion secondary battery, the controller controls that the strain energy generated in the solid electrolyte layer accompanying charging of the all-solid-state lithium-ion secondary battery causes the solid-state A first threshold temperature is calculated from a temperature lower than the crack growth energy calculated from the fracture toughness value of the electrolyte layer, and the all-solid lithium ion secondary battery is heated so as to exceed the calculated first threshold temperature. Control the temperature.

An all-solid-state lithium-ion secondary battery charging device according to another aspect of the present invention includes a charger for charging the all-solid-state lithium-ion secondary battery, and a temperature detector for detecting the temperature of the all-solid-state lithium-ion secondary battery. a temperature control unit that adjusts the temperature of the all-solid-state lithium ion secondary battery; and a control unit that controls the temperature of the all-solid-state lithium ion secondary battery. Then, when the charger charges the all-solid-state lithium-ion secondary battery, the controller controls that the strain energy generated in the solid electrolyte layer accompanying charging of the all-solid-state lithium-ion secondary battery causes the solid-state A first threshold temperature is calculated from a temperature lower than the crack growth energy calculated from the fracture toughness value of the electrolyte layer, and the all-solid lithium ion secondary battery is heated so as to exceed the calculated first threshold temperature. Control the temperature.

According to yet another aspect of the present invention, a "method for charging an all-solid-state lithium-ion secondary battery" includes charging the all-solid-state lithium-ion secondary battery when a charger charges the all-solid-state lithium-ion secondary battery. The first threshold temperature is calculated from the temperature at which the strain energy generated in the solid electrolyte layer due to the and controlling the temperature of the all-solid-state lithium-ion secondary battery so as to exceed the threshold temperature.

According to the present invention, in an all-solid-state battery using metallic lithium or a lithium-containing alloy as a negative electrode active material, it is possible to continue the charging process even if the electrolytic deposition occurs on the premise that metallic lithium is electrodeposited. It becomes possible. As a result, the large capacity of these negative electrode active materials can be fully utilized, which contributes to significant improvement in the output density and energy density of the battery.

1 is a block diagram for explaining the configuration of an all solid state lithium ion secondary battery system according to one embodiment of the present invention; FIG. As an example of a second map, it is a graph showing the temperature dependence of the Young's modulus E(Li) of the negative electrode active material layer (here, metallic lithium) when metallic lithium is used as the negative electrode active material. 4 is a flowchart showing a procedure of charging processing in the secondary battery system; A graph for explaining an example of a method of calculating the battery temperature T from the measured temperature _Tm of the secondary battery by a temperature sensor (the vertical axis is the temperature; the horizontal axis is the position inside the battery where the battery temperature T to be calculated (temperature estimation position). 1 is a cross-sectional view schematically showing a bipolar all-solid-state lithium-ion secondary battery (bipolar secondary battery) according to an embodiment of the present invention; FIG. 1 is a perspective view showing the appearance of a flat lithium-ion secondary battery, which is a representative embodiment of a bipolar secondary battery; FIG. 1 is a perspective view showing the appearance of a flat lithium-ion secondary battery, which is a representative embodiment of a bipolar secondary battery; FIG.

Hereinafter, the above-described embodiments of the present invention will be described with reference to the drawings, but the technical scope of the present invention should be determined based on the description of the claims and is not limited only to the following embodiments. Hereinafter, the present invention will be described by taking a bipolar all-solid lithium ion secondary battery, which is one form of secondary battery, as an example. Note that the dimensional ratios in the drawings are exaggerated for convenience of explanation, and may differ from the actual ratios.

[Secondary battery system]
FIG. 1 is a block diagram for explaining the configuration of an all solid state lithium ion secondary battery system according to one embodiment of the present invention.

This all solid lithium ion secondary battery system (hereinafter also referred to as "secondary battery system 1") includes an all solid lithium ion secondary battery (hereinafter also referred to as "secondary battery 2"). A voltage sensor 3 for measuring the cell voltage (inter-terminal voltage) of the secondary battery 2, a temperature sensor 4 for measuring the outer surface temperature (environmental temperature) of the secondary battery 2, and charging power are supplied to the secondary battery 2. A voltage/current adjusting unit 5, a current sensor 6 for measuring the charging/discharging current of the secondary battery 2, a heater 7 capable of heating the secondary battery 2, and a control unit 8 for controlling the temperature and charging/discharging of the secondary battery 2 are provided. Prepare. The voltage/current adjuster 5 is connected to an external power supply 9 and receives power during charging, and discharges to the external power supply 9 via the voltage/current adjuster 5 during discharging (details will be described later).

The details of each part will be described below.

The secondary battery 2 is a normal all-solid lithium ion secondary battery, and includes a positive electrode including a positive electrode active material layer containing a positive electrode active material, a negative electrode including a negative electrode active material layer containing a negative electrode active material, and the positive electrode and a solid electrolyte layer interposed between the active material layer and the negative electrode active material layer. The details of the all-solid lithium ion secondary battery will be described later.

The voltage sensor 3 may be a voltmeter, for example, and measures the cell voltage (inter-terminal voltage) between the positive electrode and the negative electrode of the secondary battery 2 . The mounting position of the voltage sensor 3 is not particularly limited as long as it can measure the cell voltage between the positive electrode and the negative electrode in the circuit connected to the secondary battery 2 .

A temperature sensor 4 measures the outer surface temperature (environmental temperature) of the secondary battery 2 . The temperature sensor 4 is attached, for example, to the surface of the case (exterior body, housing) of the secondary battery 2 . In the present embodiment, the temperature of the secondary battery 2 is obtained by estimating the temperature inside the secondary battery 2 by the control unit 8, which will be described later, from the outer surface temperature of the secondary battery 2 measured by the temperature sensor 4. do. That is, temperature sensor 4 and control unit 8 function as a temperature detection unit that detects the temperature of secondary battery 2 .

When charging the secondary battery 2 , the voltage/current adjusting unit 5 adjusts the voltage and current of the power from the external power source 9 based on the command from the control unit 8 and supplies the power to the secondary battery 2 . Further, when the secondary battery 2 is discharged, the voltage/current adjustment unit 5 discharges the electricity discharged from the secondary battery 2 to the external power supply 9 . In this manner, the voltage/current adjusting unit 5 , the external power supply 9 and the control unit 8 described later function as a charger that charges the secondary battery 2 .

Here, the external power supply 9 is a power supply for an electric vehicle called a so-called power supply grid used for charging an electric vehicle or the like, and outputs direct current. Such a power source for an electric vehicle converts commercial power (AC) into a DC voltage and current necessary for charging the secondary battery 2 and provides the DC power. In addition, the external power supply 9 has a power regeneration function, and when the secondary battery 2 discharges, it can convert direct current to alternating current and regenerate it to the commercial power supply. As a device constituting such an external power supply 9, a well-known power supply with a power regeneration function may be used, so a detailed description is omitted here (a power supply with a power regeneration function includes: For example, Japanese Unexamined Patent Publication No. 7-222369, Japanese Unexamined Patent Publication No. 10-080067, etc.).

When the external power supply 9 is not connected to an external power supply device such as a commercial power supply, for example, when charging the secondary battery 2 by using another secondary battery installed outside as a power supply, the power discharged from the secondary battery 2 is preferably stored in another secondary battery. This can reduce the waste of energy.

The current sensor 6 is, for example, an ammeter. The current sensor 6 measures the current value of the power supplied from the voltage/current adjustment unit 5 to the secondary battery 2 when the secondary battery 2 is charged, and is supplied from the secondary battery 2 to the voltage/current adjustment unit 5 when the secondary battery 2 is discharged. Measure the current value of power. The mounting position of the current sensor 6 is not particularly limited, as long as it is placed in the circuit that supplies power from the voltage/current adjustment unit 5 to the secondary battery 2 and the current value during charging and discharging can be measured. good.

The heater 7 functions as heating means for heating the secondary battery 2 . Any conventionally known heater can be preferably used as the heater. Although the heater 7 is used as a heating means for heating the secondary battery 2 in this embodiment, a heating means other than the heater may be used. For example, when the secondary battery system 1 is mounted on a vehicle, the secondary battery 2 may be heated using the heat of the exhaust gas from the vehicle on which the system is mounted. Thus, the heating means such as the heater 7 and the control section 8 described later function as a temperature control section that controls the temperature of the secondary battery 2 .

The control unit 8 is, for example, a so-called computer that includes a CPU 81, a storage unit 82, and the like. The control unit 8 controls the temperature of the secondary battery 2 when charging the secondary battery 2 according to the procedure described later. The control unit 8 also controls the conditions of the charging process. As such a control unit 8, for example, an ECU (Electronic Control Unit) may be used in an electric vehicle. When the secondary battery 2 is mounted on the vehicle, the secondary battery 2 and the control unit 8 may be mounted on the vehicle, and the charger may be installed outside the vehicle. Alternatively, the charger may be installed outside the vehicle, and the controller 8 may also be mounted on the charger.

Here, the storage unit 82 includes a RAM used as a working area by the CPU 81 as well as a non-volatile memory. The nonvolatile memory stores a program for controlling the temperature of the secondary battery 2 and controlling the charging process conditions in this embodiment.

Further, the storage unit 82 stores a map (hereinafter also referred to as "first map") showing the relationship between the battery voltage V of the secondary battery 2 and the state of charge (SOC) of the secondary battery. ) is remembered. Further, the storage unit 82 stores a map (hereinafter also referred to as “second map”) showing the temperature dependence of the Young's modulus E in the negative electrode active material layer that constitutes the secondary battery 2 . FIG. 2 is a graph showing the temperature dependence of the Young's modulus E(Li) of the negative electrode active material layer (here, metallic lithium) when metallic lithium is used as the negative electrode active material, as an example of the second map. As shown in FIG. 2, the value of the Young's modulus E(Li) of metallic lithium used as the negative electrode active material in this embodiment changes with changes in temperature (that is, shows temperature dependence). Specifically, the value of the Young's modulus E of metallic lithium sharply decreases at about 80°C. In addition to the above map, the storage unit 82 also stores the value of the crack growth energy Ψ of the solid electrolyte layer. Here, the value of the crack growth energy Ψ of the solid electrolyte layer is calculated from the value of the fracture toughness value K _1C [Pa·m ^1/2 ] of the solid electrolyte layer, and is almost unique once the material of the solid electrolyte layer is determined. It is a determined parameter, and its temperature dependence can be ignored. Specifically, the value of the crack growth energy Ψ of the solid electrolyte layer is
ψ=(K _1C ) ² /E′
can be calculated according to the formula, where E' is
E′=E/(1−ν) ²
is a value calculated according to the formula At this time, E is the Young's modulus [Pa] of the solid electrolyte layer, and ν is the Poisson's ratio of the solid electrolyte layer.

[Charging process]
A charging process procedure in the secondary battery system 1 configured in this way will be described.

This charging process is performed in a state where the secondary battery system 1 is connected to the external power supply 9 and charging power can be supplied to the secondary battery 2 . Further, the control of the charging process in this embodiment is a constant current (CC) charging method that is performed until the voltage of the secondary battery 2 reaches a predetermined voltage. However, the form of the charging process is not limited to this. A current-constant voltage (CC-CV) charging scheme may be used.

In the charging process in the present embodiment, the strain energy generated in the solid electrolyte layer that constitutes the secondary battery 2 as the secondary battery 2 is charged is greater than the crack growth energy calculated from the fracture toughness value of the solid electrolyte layer. A first threshold temperature is calculated from the temperature at which the temperature becomes smaller, and the temperature of the secondary battery 2 is controlled so as to exceed the calculated first threshold temperature. Note that the control unit 8 controls the charging process and the temperature of the secondary battery unless otherwise specified. The procedure of this charging process will be described below with reference to FIG. FIG. 3 is a flow chart showing the procedure of the charging process in the secondary battery system 1. As shown in FIG.

First, the control unit 8 starts control for charging the secondary battery 2 (step S101). Specifically, electric power is introduced from the external power supply 9 to the voltage/current adjusting unit 5 to start the charging process (in this embodiment, constant current (CC) charging is started).

Subsequently, the controller 8 obtains the charging current I from the current sensor 6, the measured temperature _Tm from the temperature sensor 4, and the battery voltage V from the voltage sensor 3 (step S102). Then, in the present embodiment, the control unit 8 stores the “map indicating the relationship between the battery voltage V of the secondary battery 2 and the state of charge (SOC) of the secondary battery 2” (first map) stored in the storage unit 82. , and based on the battery voltage V obtained from the voltage sensor 3, the SOC of the secondary battery 2 is calculated and obtained. Further, in the present embodiment, the control unit 8 calculates and acquires the internal temperature (battery temperature T) of the secondary battery 2 from the measured temperature _Tm acquired from the temperature sensor 4 . At this time, the control unit 8 controls the temperature of the secondary battery detected by the temperature sensor 4 based on the thermal resistance value (thermal conductivity) between the position where the temperature is detected by the temperature sensor 4 and the power generation element of the secondary battery 2. Correct the temperature _Tm . Here, FIG. 4 is a graph for explaining an example of a method of calculating the battery temperature T from the temperature _Tm of the secondary battery 2 measured by the temperature sensor 4 (the vertical axis is the temperature; the horizontal axis is the battery temperature T to be calculated). is the position inside the battery (distance from the position where the temperature is estimated). As shown in FIG. 4, the distance from the temperature estimation position to the battery surface is Δx ₁ , the distance from the battery surface to the measurement position (for example, the surface of the battery case) from the battery surface is Δx ₂ , and both sides of the battery surface are be T _s1 and T _s2 (T _s1 >T _s2 ), respectively. Then the heat transfer coefficients h ₁ and h ₂ respectively at the battery surface and the battery case surface, which are all known parameters, the thermal conductivity λ _c at the battery, the thermal conductivity λ _M from the battery to the measuring point, and the measured With temperature _Tm and ambient temperature _T∞ , the heat flux J in this system is
J=λ _c (TT _s1 )/Δx ₁
J=h ₁ (Ts ₁ −Ts ₂ )
J=λ _M (Ts ₂ −T _∞ )/Δx ₂
J=h ₂ (T _m −T _∞ )
is represented as By solving these for T, the battery temperature T can be calculated. By performing the following control using the battery temperature T corrected in this way, it is possible to perform more precise control and more reliably prevent the occurrence of a short circuit due to the growth of dendrites.

Subsequently, the control unit 8 calculates the deposition rate of metallic lithium in the negative electrode active material layer based on the charging current I obtained above or its integrated value (step S103). In the negative electrode active material layer according to the present embodiment, since the deposition of metallic lithium proceeds with the progress of charging, the amount of metallic lithium deposited can be calculated from the magnitude of the charging current I or its integrated value. is. After calculating the deposition rate of metallic lithium, the control unit 8 calculates the amount of metallic lithium deposited at that time, and further calculates the value of strain generated in the solid electrolyte layer based on the calculated value. The value of the strain generated in the solid electrolyte layer may be obtained directly by installing a strain gauge on the secondary battery 2 . After that, the controller 8 calculates the strain energy U as an integral value of the elastic deformation region of the stress-strain curve from the value of the strain generated in the solid electrolyte layer (step S103). Here, in the elastic deformation region of the stress-strain curve, the stress σ and strain ε are in a proportional relationship (σ=E×ε) via Young's modulus E as a constant of proportionality. Therefore, the control unit 8 creates a map (second map) showing the temperature dependence of the Young's modulus E(Li) of the negative electrode active material layer (here, metallic lithium) when metallic lithium is used as the negative electrode active material. With reference to this, the value of Young's modulus E(Li) corresponding to the battery temperature T is obtained, and the strain energy U as an integral value of the elastic deformation region of the stress-strain curve is calculated according to the following formula.

U=1/2×E× ^ε2
It is possible that metallic lithium is not uniformly deposited over the entire surface of the negative electrode active material layer (the deposition amount varies depending on the part of the negative electrode active material layer). A permissible variation between parts is set in advance, and the strain value at the part of the solid electrolyte layer corresponding to the part where the amount of metallic lithium deposited is maximum within the range of the variation is used as a representative value. may be used to calculate the strain energy U.

After that, the control unit 8 refers to the value of the crack growth energy Ψ of the solid electrolyte layer stored in the storage unit 82 and the second map described above, and converts the value of the strain generated in the solid electrolyte layer to the above measured value. , when the battery temperature T changes, the strain energy U (calculated in step S103) that similarly changes through changes in the Young's modulus E (Li) of the negative electrode active material layer changes to A temperature (T _K (U<Ψ); hereinafter also simply referred to as “T _K ”) at which the crack growth energy Ψ becomes smaller is calculated as a first threshold temperature (step S104). If the battery temperature T is higher than the first threshold temperature (T _K ) calculated in this way, the strain energy U generated in the solid electrolyte layer due to the electrodeposition of the negative electrode active material layer (metallic lithium) is Since it is smaller than the crack propagation energy Ψ in the electrolyte layer, controlling the battery temperature T to such a value can prevent crack propagation in the solid electrolyte layer caused by electrodeposited metallic lithium. This specific control will be described below with reference to FIG.

First, the control unit 8 compares the battery temperature T obtained above with the calculated T _K to determine whether or not T is greater than T _K (T>T _K ) (step S105). Here, if it is determined that T is greater than T _K (T>T _K ) (S105: YES), the control based on the battery temperature T is terminated and the process proceeds to the next step. In these flows, since the battery temperature T is sufficiently high, metallic lithium electrodeposited in the negative electrode active material layer grows in the thickness direction of the battery, and cracks in the solid electrolyte layer due to the electrolytically deposited metallic lithium progress. It means that it is considered that there is no risk of In this case, the control unit 8 determines that the SOC value of the secondary battery 2 calculated in step S102 is larger than the target SOC set in advance as a sufficient value to end the charging process (SOC>target SOC ) (step S106). Here, if it is determined that the SOC value of the secondary battery 2 is greater than the target SOC (SOC>target SOC) (S106: YES), the control unit 8 controls the voltage/current adjustment unit 5 to perform charging. The process ends (step S107).

On the other hand, if it is not determined in step S107 that the SOC value of the secondary battery 2 is greater than the target SOC (SOC>target SOC) (S106: NO), the controller 8 repeats the control from step S102.

Further, if it is not determined in step S105 that T is greater than T _K (T>T _K ) (S105: NO), the control unit 8 controls the heater 7 to raise the battery temperature T. The battery 2 is heated (step S108). Further, in this embodiment, the control unit 8 controls the voltage/current adjustment unit 5 so as to reduce the charging current in this case. After that, the control unit 8 repeats the control from step S105. In the present invention, it is essential to control the heating of the secondary battery 2, but it is not necessary to control the charging conditions. In step S108, the control unit 8 controls the heater 7 to heat the secondary battery 2. In the present embodiment, the heater 7 controls the temperature of the positive electrode side of the single cell constituting the secondary battery 2 to the negative electrode temperature. The secondary battery 2 is arranged so as to be able to heat the secondary battery 2 so as to be higher than the temperature on the side. With such a configuration, the tip of the dendrite of metallic lithium grown from the negative electrode active material layer side is exposed to a higher temperature as it approaches the positive electrode active material layer. Since the mechanical properties (Young's modulus) of metallic lithium exposed to higher temperatures become smaller values, it is possible to further reduce the possibility that dendrites reach the positive electrode active material layer.

Although the control according to the present invention has been described in detail above, the embodiment described with reference to the drawings is merely an example, and can be modified as appropriate within the scope of the technical concept of the invention described in the claims. You may carry out this invention. For example, in the above-described embodiment, the temperature (T _K (U<Ψ)) at which the strain energy U generated in the solid electrolyte layer as the secondary battery 2 is charged becomes smaller than the crack growth energy Ψ of the solid electrolyte layer is The temperature obtained by multiplying T _K (U<Ψ) by a predetermined safety factor or the temperature obtained by adding a predetermined temperature range to T _K (U<Ψ) was used as the first threshold temperature. may be adopted as

In addition, according to another aspect of the present invention, there is provided a charging device for charging the secondary battery 2 described above (charging device for all-solid-state lithium-ion secondary battery). A charging device for charging an all-solid-state lithium-ion secondary battery includes a charger for charging the all-solid-state lithium-ion secondary battery, a temperature detection unit for detecting the temperature of the all-solid-state lithium-ion secondary battery, and the all-solid-state lithium ion secondary battery. A temperature control unit that adjusts the temperature of the solid state lithium ion secondary battery, and the solid electrolyte that accompanies charging of the all solid state lithium ion secondary battery when the charger charges the all solid state lithium ion secondary battery. A first threshold temperature is calculated from the temperature at which the strain energy generated in the layer becomes smaller than the crack growth energy calculated from the fracture toughness value of the solid electrolyte layer, and the calculated first threshold temperature is exceeded. and a control unit for controlling the temperature of the all solid state lithium ion secondary battery.

Further, according to still another aspect of the present invention, a secondary battery charging method for charging the secondary battery 2 described above is also provided. A charging method for an all-solid-state lithium ion secondary battery includes strain energy generated in the solid electrolyte layer accompanying charging of the all-solid-state lithium-ion secondary battery when a charger charges the all-solid-state lithium ion secondary battery. is calculated from the temperature at which the crack growth energy calculated from the fracture toughness value of the solid electrolyte layer becomes smaller than the first threshold temperature, and the all-solid lithium ion It includes controlling the temperature of the secondary battery.

The constituent elements of the all-solid-state lithium-ion secondary battery system according to this embodiment will be described below. In this specification, the bipolar all-solid lithium ion secondary battery is also simply referred to as "bipolar secondary battery", and the electrode for bipolar all-solid lithium ion secondary battery is simply referred to as "bipolar electrode". There is

<Bipolar secondary battery>
FIG. 6 is a cross-sectional view schematically showing a bipolar all-solid-state lithium-ion secondary battery (bipolar secondary battery) according to an embodiment of the present invention. A bipolar secondary battery 10 shown in FIG. 6 has a structure in which a substantially rectangular power generation element 21 in which charge/discharge reactions actually progress is sealed inside a laminate film 29 that is a battery exterior body.

As shown in FIG. 6, the power generation element 21 of the bipolar secondary battery 10 of the present embodiment has the positive electrode active material layer 13 electrically coupled to one surface of the current collector 11, and the current collector 11 It has a plurality of bipolar electrodes 23 with a negative electrode active material layer 15 electrically coupled to the opposite surface. Each bipolar electrode 23 is laminated via the solid electrolyte layer 17 to form the power generation element 21 . In addition, the solid electrolyte layer 17 has a structure in which a solid electrolyte is formed into a layer. At this time, the positive electrode active material layer 13 of one bipolar electrode 23 and the negative electrode active material layer 15 of the other bipolar electrode 23 adjacent to the one bipolar electrode 23 face each other with the solid electrolyte layer 17 interposed therebetween. , bipolar electrodes 23 and solid electrolyte layers 17 are alternately stacked. That is, the solid electrolyte layer 17 is sandwiched between the positive electrode active material layer 13 of one bipolar electrode 23 and the negative electrode active material layer 15 of the other bipolar electrode 23 adjacent to the one bipolar electrode 23. It is However, the technical scope of the present invention is not limited to the bipolar secondary battery as shown in FIG. may be

Adjacent positive electrode active material layer 13 , solid electrolyte layer 17 , and negative electrode active material layer 15 constitute one cell layer 19 . Therefore, it can be said that the bipolar secondary battery 10 has a structure in which the cell layers 19 are stacked. The positive electrode active material layer 13 is formed only on one side of the outermost current collector 11 a on the positive electrode side located in the outermost layer of the power generating element 21 . In addition, the negative electrode active material layer 15 is formed only on one side of the outermost current collector 11b on the negative electrode side located in the outermost layer of the power generating element 21 .

Furthermore, in the bipolar secondary battery 10 shown in FIG. 6, a positive electrode current collector plate (positive electrode tab) 25 is arranged adjacent to the outermost layer current collector 11a on the positive electrode side, and this is extended to form the battery exterior. It is led out from the laminate film 29 . On the other hand, a negative electrode current collector plate (negative electrode tab) 27 is arranged adjacent to the outermost layer current collector 11 b on the negative electrode side, and is similarly extended to lead out from the laminate film 29 .

Note that the number of times the cell layers 19 are stacked is adjusted according to the desired voltage. Moreover, in the bipolar secondary battery 10, the number of times the cell layers 19 are stacked may be reduced if sufficient output can be secured even if the thickness of the battery is made as thin as possible. In the bipolar secondary battery 10 as well, in order to prevent external impact and environmental deterioration during use, the power generating element 21 is enclosed under reduced pressure in a laminate film 29 that is a battery outer body, and a positive current collector plate 25 and a negative electrode collector are enclosed. A structure in which the electric plate 27 is taken out of the laminate film 29 is preferable.

The main components of the bipolar secondary battery described above will be described below.

[Current collector]
The current collector has a function of mediating transfer of electrons from one surface in contact with the positive electrode active material layer to the other surface in contact with the negative electrode active material layer. There are no particular restrictions on the material that constitutes the current collector. As the constituent material of the current collector, for example, a metal or a conductive resin can be used.

Specifically, examples of metals include aluminum, nickel, iron, stainless steel, titanium, and copper. In addition to these, a clad material of nickel and aluminum, a clad material of copper and aluminum, or the like may be used. Alternatively, a foil in which a metal surface is coated with aluminum may be used. Among them, aluminum, stainless steel, copper, and nickel are preferable from the viewpoint of electronic conductivity, battery operating potential, adhesion of the negative electrode active material to the current collector by sputtering, and the like.

As the latter conductive resin, a resin obtained by adding a conductive filler to a non-conductive polymeric material as necessary can be used.

Examples of non-conductive polymer materials include polyethylene (PE; high-density polyethylene (HDPE), low-density polyethylene (LDPE), etc.), polypropylene (PP), polyethylene terephthalate (PET), polyethernitrile (PEN), and polyimide. (PI), polyamideimide (PAI), polyamide (PA), polytetrafluoroethylene (PTFE), styrene-butadiene rubber (SBR), polyacrylonitrile (PAN), polymethylacrylate (PMA), polymethylmethacrylate (PMMA) , polyvinyl chloride (PVC), polyvinylidene fluoride (PVdF), or polystyrene (PS). Such non-conductive polymeric materials can have excellent electrical potential or solvent resistance.

Conductive fillers may be added to the conductive polymer material or non-conductive polymer material as necessary. In particular, when the resin serving as the base material of the current collector consists of only a non-conductive polymer, a conductive filler is inevitably essential in order to impart conductivity to the resin.

Any electrically conductive filler can be used without particular limitation. Examples of materials having excellent conductivity, potential resistance, or lithium ion blocking properties include metals and conductive carbon. The metal is not particularly limited, but includes at least one metal selected from the group consisting of Ni, Ti, Al, Cu, Pt, Fe, Cr, Sn, Zn, In, and Sb, or these metals. It preferably contains alloys or metal oxides. Also, the conductive carbon is not particularly limited. Preferably, it is selected from the group consisting of acetylene black, Vulcan (registered trademark), Black Pearl (registered trademark), carbon nanofiber, Ketjenblack (registered trademark), carbon nanotube, carbon nanohorn, carbon nanoballoon, and fullerene. At least one type is included.

The amount of the conductive filler added is not particularly limited as long as it is an amount that can impart sufficient conductivity to the current collector, and is generally 5 to 80% by mass with respect to 100% by mass of the total mass of the current collector. is.

The current collector may have a single-layer structure made of a single material, or may have a laminated structure in which layers made of these materials are appropriately combined. From the viewpoint of reducing the weight of the current collector, it is preferable to include at least a conductive resin layer made of a resin having conductivity. Moreover, from the viewpoint of blocking movement of lithium ions between the single cell layers, a metal layer may be provided on a part of the current collector.

[Negative electrode active material layer]
The negative electrode active material layer contains a negative electrode active material. In the present invention, the negative electrode active material essentially contains metallic lithium or a lithium-containing alloy. The types of these negative electrode active materials are not particularly limited, but examples of Li-containing alloys include alloys of Li and at least one of In, Al, Si and Sn. In some cases, two or more kinds of negative electrode active materials may be used together. Needless to say, negative electrode active materials other than those described above may be used as long as they essentially contain metallic lithium or a lithium-containing alloy.

Examples of the shape of the negative electrode active material include particulate (spherical, fibrous), thin film, and the like. When the negative electrode active material is in the form of particles, its average particle size (D ₅₀ ) is, for example, preferably in the range of 1 nm to 100 μm, more preferably in the range of 10 nm to 50 μm, still more preferably 100 nm. to 20 μm, particularly preferably 1 to 20 μm. In addition, in this specification, the value of the average particle size (D ₅₀ ) of the active material can be measured by a laser diffraction scattering method.

The content of the negative electrode active material in the negative electrode active material layer is not particularly limited. more preferred.

The negative electrode active material layer preferably further contains a solid electrolyte. By including the solid electrolyte in the negative electrode active material layer, the ion conductivity of the negative electrode active material layer can be improved. Solid electrolytes include, for example, sulfide solid electrolytes and oxide solid electrolytes. Generally, they are not easily affected by grain boundaries, so they have a substantial fracture toughness value (i.e., cracks caused by dendrites). from the viewpoint of high ionic conductivity), it is preferable to contain a sulfide solid electrolyte.

Examples of sulfide solid electrolytes include LiI—Li ₂ S—SiS ₂ , LiI—Li ₂ SP ₂ O ₅ , LiI—Li ₃ PO ₄ —P ₂ S ₅ , Li ₂ SP ₂ S ₅ , LiI _{- Li3PS4} , _{LiI - LiBr - Li3PS4 , Li3PS4 , Li2SP2S5 , Li2SP2S5} -LiI _{, Li2SP2S5-} Li ₂ O, Li ₂ SP ₂ S ₅ —Li ₂ O—LiI, Li ₂ S—SiS ₂ , Li ₂ S—SiS ₂ —LiI, Li ₂ S—SiS ₂ —LiBr, Li ₂ S—SiS ₂ -LiCl, _Li2S - _SiS2 - _{B2S3 - LiI} , _{Li2S - SiS2 - P2S5} -LiI, _Li2S - _B2S3 , _{Li2SP2S5 -} Z _m S _n (where m and n are positive numbers and Z is one of Ge, Zn and Ga), Li ₂ S—GeS ₂ , Li ₂ S—SiS ₂ —Li ₃ PO ₄ , Li ₂ S—SiS ₂ —Li _x MO _y (where x and y are positive numbers and M is any one of P, Si, Ge, B, Al, Ga and In), and the like. . The description of “Li ₂ SP ₂ S ₅ ” means a sulfide solid electrolyte using a raw material composition containing Li ₂ S and P ₂ S ₅ , and the same applies to other descriptions.

The sulfide solid electrolyte may have, for example, a Li ₃ PS ₄ skeleton, a Li ₄ P ₂ S ₇ skeleton, or a Li ₄ P ₂ S ₆ skeleton. . Examples of sulfide solid electrolytes having a Li ₃ PS ₄ skeleton include LiI--Li ₃ PS ₄ , LiI--LiBr--Li ₃ PS _{4 and} Li ₃ PS ₄ . Examples of sulfide solid electrolytes having a Li ₄ P ₂ S ₇ skeleton include Li—P—S solid electrolytes called LPS (eg, Li ₇ P ₃ S ₁₁ ). As the sulfide solid electrolyte, for example, LGPS represented by Li _(4-x) Ge _(1-x) P _x S ₄ (where x satisfies 0<x<1) may be used. Among them, the sulfide solid electrolyte is preferably a sulfide solid electrolyte containing the element P, and more preferably a material containing Li ₂ SP ₂ S ₅ as a main component. Furthermore, the sulfide solid electrolyte may contain halogens (F, Cl, Br, I).

When the sulfide solid electrolyte is Li ₂ S—P ₂ S ₅ system, the molar ratio of Li ₂ S and P ₂ S ₅ is Li ₂ S:P ₂ S ₅ =50:50 to 100. :0, and more preferably Li ₂ S:P ₂ S ₅ =70:30 to 80:20.

The sulfide solid electrolyte may be sulfide glass, crystallized sulfide glass, or a crystalline material obtained by a solid phase method. The sulfide glass can be obtained, for example, by subjecting the raw material composition to mechanical milling (such as a ball mill). Crystallized sulfide glass can be obtained, for example, by heat-treating sulfide glass at a temperature equal to or higher than the crystallization temperature. Further, the ionic conductivity (eg, Li ion conductivity) of the sulfide solid electrolyte at room temperature (25° C.) is, for example, preferably 1×10 ⁻⁵ S/cm or more, and 1×10 ⁻⁴ S/cm. cm or more is more preferable. Incidentally, the value of the ionic conductivity of the solid electrolyte can be measured by the AC impedance method.

Examples of oxide solid electrolytes include compounds having a NASICON structure. Examples of compounds having a NASICON structure include compounds represented by the general formula Li _1+x Al _x Ge _2-x (PO ₄ ) ₃ (0≦x≦2) (LAGP) and general formula Li _1+x Al _x Ti _{2 -x} (PO ₄ ) ₃ (0≦x≦2) (LATP) and the like. Other examples of oxide solid electrolytes include LiLaTiO (e.g., Li _0.34 La _0.51 TiO ₃ ), LiPON (e.g., Li _2.9 PO _3.3 N _0.46 ), LiLaZrO (e.g., , Li ₇ La ₃ Zr ₂ O ₁₂ ) and the like.

Examples of the shape of the solid electrolyte include particle shapes such as spherical and ellipsoidal shapes, and thin film shapes. When the solid electrolyte is in the form of particles, the average particle size (D ₅₀ ) is not particularly limited, but is preferably 40 μm or less, more preferably 20 μm or less, and even more preferably 10 μm or less. On the other hand, the average particle diameter (D ₅₀ ) is preferably 0.01 μm or more, more preferably 0.1 μm or more.

The content of the solid electrolyte in the negative electrode active material layer is, for example, preferably in the range of 1 to 60% by mass, more preferably in the range of 10 to 50% by mass.

The negative electrode active material layer may further contain at least one of a conductive aid and a binder in addition to the negative electrode active material and solid electrolyte described above.

Examples of conductive aids include metals such as aluminum, stainless steel (SUS), silver, gold, copper, and titanium, alloys containing these metals, and metal oxides; carbon fibers (specifically, vapor-grown carbon fibers (VGCF), polyacrylonitrile-based carbon fiber, pitch-based carbon fiber, rayon-based carbon fiber, activated carbon fiber, etc.), carbon nanotubes (CNT), carbon black (specifically, acetylene black, Ketjenblack (registered trademark) , furnace black, channel black, thermal lamp black, etc.), but are not limited thereto. In addition, a particulate ceramic material or resin material coated with the above metal material by plating or the like can also be used as a conductive aid. Among these conductive aids, from the viewpoint of electrical stability, it is preferable to include at least one selected from the group consisting of aluminum, stainless steel, silver, gold, copper, titanium, and carbon. , silver, gold, and carbon, and more preferably at least one carbon. These conductive aids may be used alone or in combination of two or more.

The shape of the conductive aid is preferably particulate or fibrous. When the conductive agent is particulate, the shape of the particles is not particularly limited, and may be powdery, spherical, rod-like, needle-like, plate-like, columnar, amorphous, scaly, spindle-like, or the like. I don't mind.

The average particle size (primary particle size) of the conductive additive in the form of particles is not particularly limited, but is preferably 0.01 to 10 μm from the viewpoint of the electrical characteristics of the battery. In this specification, the "particle diameter of the conductive aid" means the maximum distance L among the distances between any two points on the outline of the conductive aid. The value of the "average particle size of the conductive aid" is the particle size of particles observed in several to several tens of fields using observation means such as a scanning electron microscope (SEM) or a transmission electron microscope (TEM). shall be calculated as the average value of

When the negative electrode active material layer contains a conductive agent, the content of the conductive agent in the negative electrode active material layer is not particularly limited, but is preferably 0 to 10% by mass with respect to the total mass of the negative electrode active material layer. , more preferably 2 to 8% by mass, more preferably 4 to 7% by mass. Within such a range, it becomes possible to form a stronger electron conduction path in the negative electrode active material layer, which can effectively contribute to the improvement of battery characteristics.

On the other hand, the binder is not particularly limited, but includes, for example, the following materials.

Polybutylene terephthalate, polyethylene terephthalate, polyvinylidene fluoride (PVDF) (including compounds in which hydrogen atoms are replaced with other halogen elements), polyethylene, polypropylene, polymethylpentene, polybutene, polyethernitrile, polytetrafluoroethylene, Polyacrylonitrile, polyimide, polyamide, ethylene-vinyl acetate copolymer, polyvinyl chloride, styrene-butadiene rubber (SBR), ethylene-propylene-diene copolymer, styrene-butadiene-styrene block copolymer and hydrogenated products thereof , thermoplastic polymers such as styrene/isoprene/styrene block copolymers and their hydrogenated products, tetrafluoroethylene/hexafluoropropylene copolymers (FEP), tetrafluoroethylene/perfluoroalkyl vinyl ether copolymers (PFA) , ethylene/tetrafluoroethylene copolymer (ETFE), polychlorotrifluoroethylene (PCTFE), ethylene/chlorotrifluoroethylene copolymer (ECTFE), fluorine resins such as polyvinyl fluoride (PVF), vinylidene fluoride- Hexafluoropropylene fluororubber (VDF-HFP fluororubber), vinylidene fluoride-hexafluoropropylene-tetrafluoroethylene fluororubber (VDF-HFP-TFE fluororubber), vinylidene fluoride-pentafluoropropylene fluororubber (VDF-PFP fluororubber), vinylidene fluoride-pentafluoropropylene-tetrafluoroethylene fluororubber (VDF-PFP-TFE fluororubber), vinylidene fluoride-perfluoromethyl vinyl ether-tetrafluoroethylene fluororubber ( VDF-PFMVE-TFE fluororubber), vinylidene fluoride-chlorotrifluoroethylene fluororubber (VDF-CTFE fluororubber) and other vinylidene fluoride fluororubbers, and epoxy resins. Among them, polyimide, styrene-butadiene rubber, carboxymethylcellulose, polypropylene, polytetrafluoroethylene, polyacrylonitrile, and polyamide are more preferable.

Although the thickness of the negative electrode active material layer varies depending on the configuration of the intended all-solid-state battery, it is preferably in the range of 0.1 to 1000 μm, for example.

[Positive electrode active material layer]
The positive electrode active material layer contains a positive electrode active material. The type of positive electrode active material is not particularly limited, but layered rock salt type active materials such as LiCoO ₂ , LiMnO ₂ , LiNiO 2 , LiVO _{2 ,} Li(Ni--Mn--Co)O ₂ , LiMn ₂ O ₄ and LiNi _{0 Spinel} -type active materials such as _.5Mn1.5O4 , olivine _- type _active materials such as _LiFePO4 and _LiMnPO4 , and Si _- containing active materials such as _Li2FeSiO4 and _Li2MnSiO4 . As an oxide active material other than the above, for example, Li ₄ Ti ₅ O ₁₂ can be mentioned. Among them, composite oxides containing lithium and nickel are preferably used, and more preferably Li(Ni--Mn--Co) O ₂ and those in which a part of these transition metals are replaced with other elements (hereinafter , also simply referred to as “NMC composite oxide”) is used. The NMC composite oxide has a layered crystal structure in which a lithium atomic layer and a transition metal (Mn, Ni and Co are arranged in an orderly manner) atomic layer are alternately stacked via an oxygen atomic layer. It contains one Li atom, and the amount of Li that can be extracted is twice that of the spinel-based lithium manganese oxide, that is, the supply capacity is doubled, and a high capacity can be obtained.

NMC composite oxides also include composite oxides in which a portion of the transition metal element is replaced with another metal element, as described above. Other elements in that case include Ti, Zr, Nb, W, P, Al, Mg, V, Ca, Sr, Cr, Fe, B, Ga, In, Si, Mo, Y, Sn, V, and Cu. , Ag, Zn, etc., preferably Ti, Zr, Nb, W, P, Al, Mg, V, Ca, Sr, Cr, more preferably Ti, Zr, P, Al, Mg, Cr, more preferably Ti, Zr, Al, Mg, or Cr from the viewpoint of improving cycle characteristics.

Furthermore, it is also one of preferred embodiments that a sulfur-based positive electrode active material is used. Examples of the sulfur-based positive electrode active material include particles or thin films of organic sulfur compounds or inorganic sulfur compounds, which can release lithium ions during charging and absorb lithium ions during discharging by utilizing the oxidation-reduction reaction of sulfur. Any substance that can Examples of organic sulfur compounds include disulfide compounds, sulfur-modified polyacrylonitrile represented by compounds described in WO 2010/044437, sulfur-modified polyisoprene, rubeanic acid (dithiooxamide), polysulfide carbon, and the like. Among these, disulfide compounds, sulfur-modified polyacrylonitrile, and rubeanic acid are preferred, and sulfur-modified polyacrylonitrile is particularly preferred. As the disulfide compound, those having a dithiobiurea derivative, a thiourea group, a thioisocyanate group, or a thioamide group are more preferable. Here, sulfur-modified polyacrylonitrile is sulfur-atom-containing modified polyacrylonitrile obtained by mixing sulfur powder and polyacrylonitrile and heating the mixture under an inert gas or under reduced pressure. Its putative structure is described, for example, in Chem. Mater. 2011, 23, 5024-5028, polyacrylonitrile is ring-closed to form a polycyclic structure, and at least part of S is bonded to C. The compound described in this document has strong peak signals near 1330 cm ^-1 and 1560 cm ^-1 in the Raman spectrum, and further peaks near 307 cm ^-1 , 379 cm ^-1 , 472 cm ^-1 and 929 cm ^-1 . do. On the other hand, inorganic sulfur compounds are preferable because of their excellent stability. Specifically, sulfur (S), S-carbon composite, TiS ₂ , TiS ₃ , TiS ₄ , NiS, NiS ₂ , CuS, FeS ₂ , Li ₂ S, MoS ₂ , MoS ₃ and the like. Among them, S, S-carbon composites, TiS ₂ , TiS ₃ , TiS ₄ , FeS ₂ and MoS ₂ are preferred, and S-carbon composites, TiS ₂ and FeS ₂ are more preferred. Here, the S-carbon composite includes a sulfur powder and a carbon material, and is in a composite state by subjecting them to heat treatment or mechanical mixing. More specifically, the state in which sulfur is distributed on the surface and in the pores of the carbon material, the state in which sulfur and the carbon material are uniformly dispersed at the nano level and are aggregated into particles, and the state in which fine sulfur It is a state in which the carbon material is distributed on the surface or inside of the powder, or a state in which a plurality of these states are combined.

In some cases, two or more positive electrode active materials may be used together. It goes without saying that positive electrode active materials other than those described above may be used.

Examples of the shape of the positive electrode active material include particulate (spherical, fibrous), thin film, and the like. When the positive electrode active material is in the form of particles, its average particle size (D ₅₀ ) is, for example, preferably in the range of 1 nm to 100 μm, more preferably in the range of 10 nm to 50 μm, and still more preferably 100 nm. to 20 μm, particularly preferably 1 to 20 μm. In addition, in this specification, the value of the average particle size (D ₅₀ ) of the active material can be measured by a laser diffraction scattering method.

The content of the positive electrode active material in the positive electrode active material layer is not particularly limited. more preferred. In addition, the positive electrode active material layer may also contain at least one of a solid electrolyte, a conductive aid, and a binder, if necessary, similarly to the negative electrode active material layer described above. Since the specific forms of these materials are the same as those described above, detailed description is omitted here.

[Solid electrolyte layer]
The solid electrolyte layer of the bipolar secondary battery according to this embodiment is a layer containing a solid electrolyte as a main component and interposed between the positive electrode active material layer and the negative electrode active material layer. Since the specific form of the solid electrolyte contained in the solid electrolyte layer is the same as described above, detailed description is omitted here.

The content of the solid electrolyte in the solid electrolyte layer is, for example, preferably in the range of 10 to 100% by mass, more preferably in the range of 50 to 100% by mass, and in the range of 90 to 100% by mass. is more preferable.

The solid electrolyte layer may further contain a binder in addition to the solid electrolyte described above. Since the specific form of the binder that can be contained in the solid electrolyte layer is the same as described above, detailed description is omitted here.

The thickness of the solid electrolyte layer varies depending on the configuration of the intended bipolar secondary battery, but for example, it is preferably in the range of 0.1 to 1000 μm, more preferably in the range of 0.1 to 300 μm. is more preferred.

[Positive collector plate and negative collector plate]
The material constituting the current collectors (25, 27) is not particularly limited, and known highly conductive materials conventionally used as current collectors for secondary batteries can be used. Metal materials such as aluminum, copper, titanium, nickel, stainless steel (SUS), and alloys thereof are preferable as the constituent material of the current collector plate. From the viewpoint of light weight, corrosion resistance and high conductivity, aluminum and copper are more preferred, and aluminum is particularly preferred. The same material or different materials may be used for the positive electrode collector plate 27 and the negative electrode collector plate 25 .

[Positive lead and negative lead]
Although not shown, the current collector 11 and the current collector plates (25, 27) may be electrically connected via a positive lead or a negative lead. Materials used in known lithium-ion secondary batteries can also be employed as the constituent materials of the positive and negative electrode leads. In addition, the parts taken out from the exterior should be heat-shrunk with heat-resistant insulation so that they do not come into contact with peripheral equipment or wiring and cause electric leakage and affect the product (for example, automobile parts, especially electronic equipment, etc.). Covering with a tube or the like is preferred.

[Battery exterior body]
As the battery outer package, a known metal can case can be used, or a bag-like case using a laminate film 29 containing aluminum that can cover the power generation element as shown in FIG. 6 can be used. The laminated film may be, for example, a laminated film having a three-layer structure in which PP, aluminum and nylon are laminated in this order, but is not limited thereto. A laminate film is desirable from the viewpoint that it is excellent in high power output and cooling performance and can be suitably used for batteries for large equipment for EV and HEV. Moreover, since the group pressure applied to the power generating element from the outside can be easily adjusted, the outer package is more preferably a laminate film containing aluminum.

The bipolar secondary battery of this embodiment has a structure in which a plurality of single cell layers are connected in series, and thus has excellent output characteristics at a high rate. Therefore, the bipolar secondary battery of this embodiment is suitably used as a power source for driving EVs and HEVs.

FIG. 7 is a perspective view showing the appearance of a flat lithium-ion secondary battery, which is a representative embodiment of a bipolar secondary battery.

As shown in FIG. 7, the flat bipolar secondary battery 50 has a rectangular flat shape, and from both sides thereof, a positive electrode tab 58 and a negative electrode tab 59 for extracting electric power are pulled out. there is The power generation element 57 is wrapped by the battery outer body (laminate film 52) of the bipolar secondary battery 50, and its periphery is heat-sealed. sealed in place. Here, the power generation element 57 corresponds to the power generation element 21 of the bipolar secondary battery 10 shown in FIG. 6 described above. The power generation element 57 is formed by stacking a plurality of bipolar electrodes 23 with the solid electrolyte layer 17 interposed therebetween.

In addition, the lithium ion secondary battery is not limited to a laminated flat shape. The wound type lithium ion secondary battery may have a cylindrical shape, or may have a rectangular flat shape obtained by deforming such a cylindrical shape. etc. is not particularly limited. In the case of the cylindrical container, the exterior body may be a laminate film or a conventional cylindrical can (metal can), and is not particularly limited. Preferably, the power generating element is wrapped with an aluminum laminate film. Weight reduction can be achieved by this configuration.

Also, the removal of the tabs 58 and 59 shown in FIG. 7 is not particularly limited. The positive electrode tab 58 and the negative electrode tab 59 may be pulled out from the same side, or the positive electrode tab 58 and the negative electrode tab 59 may be divided into a plurality of pieces and pulled out from each side, as shown in FIG. is not limited to In a wound type lithium ion battery, terminals may be formed using, for example, cylindrical cans (metal cans) instead of tabs.

[Assembled battery]
An assembled battery is an object configured by connecting a plurality of batteries. Specifically, at least two or more are used, and serialization or parallelization or both of them are used. By connecting in series and in parallel, it is possible to freely adjust the capacity and voltage.

A plurality of batteries can be connected in series or in parallel to form a small detachable assembled battery. Then, a plurality of these detachable small assembled batteries are further connected in series or in parallel to form a large-capacity, large-capacity battery suitable for a vehicle drive power supply or an auxiliary power supply that requires high volumetric energy density and high volumetric output density. An assembled battery with an output can also be formed. How many batteries are connected to make an assembled battery, and how many stages of small assembled batteries are stacked to make a large-capacity assembled battery, depends on the battery capacity of the vehicle (electric vehicle) in which it is installed. It should be decided according to the output.

When the charging method according to the present invention is applied to the assembled battery, the charging process can be performed while measuring the AC impedance of each individual battery (single cell) constituting the assembled battery, for example. With such a configuration, the charging process can be performed while separately monitoring the occurrence of electrodeposition in each individual battery (single cell).

[vehicle]
The non-aqueous electrolyte secondary battery of the present embodiment maintains discharge capacity even after long-term use, and has good cycle characteristics. Furthermore, it has a high volumetric energy density. Vehicle applications such as electric vehicles, hybrid electric vehicles, fuel cell vehicles, and hybrid fuel cell vehicles require higher capacity, larger size, and longer life compared to electrical and portable electronic equipment applications. . Therefore, the non-aqueous electrolyte secondary battery can be suitably used as a power source for vehicles, for example, a power source for driving a vehicle or an auxiliary power source.

Specifically, a battery or an assembled battery formed by combining a plurality of these batteries can be mounted on a vehicle. In the present invention, it is possible to configure a long-life battery with excellent long-term reliability and output characteristics, so when such a battery is installed, a plug-in hybrid electric vehicle with a long EV driving range and an electric vehicle with a long driving range per charge can be configured. . Batteries or assembled batteries made by combining a plurality of these, for example, in the case of automobiles, hybrid vehicles, fuel cell vehicles, electric vehicles (all four-wheeled vehicles (commercial vehicles such as passenger cars, trucks, buses, light vehicles, etc.) , two-wheeled vehicles (motorcycles) and three-wheeled vehicles) will provide a long-lasting and highly reliable automobile. However, the application is not limited to automobiles, for example, it can be applied to various power sources for other vehicles, such as moving bodies such as trains, and power sources for installation such as uninterruptible power supplies. It can also be used as

When the charging method according to the present invention is applied to a battery (assembled battery) mounted on a vehicle, charging is performed under charging conditions such as rapid charging where electrodeposited metallic lithium tends to grow. Even so, there is an advantage that it is possible to fully utilize the capacity of the battery while detecting the occurrence of metallic lithium electrodeposition with high accuracy.

In the above description, the embodiment of the present invention is described by taking a bipolar secondary battery as an example, but the type of secondary battery to which the present invention can be applied is not particularly limited. So-called parallel-stacked all-solid-state batteries in which are connected in parallel, and any conventionally known bipolar or non-bipolar (parallel-stacked) non-aqueous electrolyte secondary batteries (batteries using electrolyte) Applicable.

1 all solid state lithium ion secondary battery system,
2 all-solid lithium ion secondary battery,
3 voltage sensor,
4 temperature sensor,
5 voltage and current adjustment unit,
6 current sensor,
7 heater,
8 control unit,
9 external power supply,
10, 50 bipolar secondary battery,
11 current collector,
11a outermost current collector on the positive electrode side,
11b outermost current collector on the negative electrode side,
13 positive electrode active material layer,
15 negative electrode active material layer,
17 electrolyte layer,
19 cell layer,
21, 57 power generation element,
23 bipolar electrodes,
25 positive collector plate (positive tab),
27 negative electrode current collector (negative electrode tab),
29, 52 laminate film,
58 positive tab,
59 negative tab,
81 CPUs,
82 storage unit;

Claims (6)

a positive electrode including a positive electrode active material layer containing a positive electrode active material;
a negative electrode comprising a negative electrode active material layer containing a negative electrode active material containing metallic lithium or a lithium-containing alloy;
a solid electrolyte layer interposed between the positive electrode active material layer and the negative electrode active material layer;
an all-solid lithium ion secondary battery comprising a power generation element having
a charger for charging the all-solid-state lithium-ion secondary battery;
a temperature detection unit that detects the temperature of the all-solid-state lithium ion secondary battery;
a temperature control unit that controls the temperature of the all-solid lithium ion secondary battery;
When the charger charges the all-solid-state lithium ion secondary battery, the strain energy generated in the solid electrolyte layer accompanying charging of the all-solid-state lithium ion secondary battery is calculated from the fracture toughness value of the solid electrolyte layer. A control unit that calculates a first threshold temperature from a temperature that is lower than the calculated crack growth energy, and controls the temperature of the all-solid lithium ion secondary battery so that it exceeds the calculated first threshold temperature; ,
An all-solid-state lithium-ion secondary battery system. 2. The all-solid lithium ion secondary battery system according to claim 1, wherein said solid electrolyte layer comprises a sulfide solid electrolyte. The control unit corrects the temperature of the all-solid-state lithium ion secondary battery detected by the temperature detection unit based on the thermal resistance value between the temperature detection position by the temperature detection unit and the power generation element. The all-solid lithium ion secondary battery system according to claim 1 or 2. The temperature control unit may heat the all-solid-state lithium-ion secondary battery so that the temperature on the positive electrode side of the single cell constituting the all-solid-state lithium-ion secondary battery is higher than the temperature on the negative electrode side. The all-solid lithium ion secondary battery system according to any one of claims 1 to 3, which is a heating means capable of. a positive electrode including a positive electrode active material layer containing a positive electrode active material;
a negative electrode comprising a negative electrode active material layer containing a negative electrode active material containing metallic lithium or a lithium-containing alloy;
a solid electrolyte layer interposed between the positive electrode active material layer and the negative electrode active material layer;
A charging device for charging an all-solid-state lithium ion secondary battery comprising a power generation element having
a charger for charging the all-solid-state lithium-ion secondary battery;
a temperature detection unit that detects the temperature of the all-solid-state lithium ion secondary battery;
a temperature control unit that controls the temperature of the all-solid lithium ion secondary battery;
When the charger charges the all-solid-state lithium ion secondary battery, the strain energy generated in the solid electrolyte layer accompanying charging of the all-solid-state lithium ion secondary battery is calculated from the fracture toughness value of the solid electrolyte layer. A control unit that calculates a first threshold temperature from a temperature that is lower than the calculated crack growth energy, and controls the temperature of the all-solid lithium ion secondary battery so that it exceeds the calculated first threshold temperature; ,
A charging device for an all-solid lithium ion secondary battery. a positive electrode including a positive electrode active material layer containing a positive electrode active material;
a negative electrode comprising a negative electrode active material layer containing a negative electrode active material containing metallic lithium or a lithium-containing alloy;
a solid electrolyte layer interposed between the positive electrode active material layer and the negative electrode active material layer;
A charging method for an all-solid-state lithium ion secondary battery comprising a power generating element having
When the charger charges the all-solid-state lithium ion secondary battery, the strain energy generated in the solid electrolyte layer accompanying charging of the all-solid-state lithium ion secondary battery is calculated from the fracture toughness value of the solid electrolyte layer. Calculate the first threshold temperature from the temperature lower than the crack growth energy calculated, and control the temperature of the all-solid lithium ion secondary battery to exceed the calculated first threshold temperature, A charging method for an all-solid-state lithium-ion secondary battery.

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