WO2011074199A1 - 非水電解質二次電池の充電方法、及び電池パック - Google Patents
非水電解質二次電池の充電方法、及び電池パック Download PDFInfo
- Publication number
- WO2011074199A1 WO2011074199A1 PCT/JP2010/007027 JP2010007027W WO2011074199A1 WO 2011074199 A1 WO2011074199 A1 WO 2011074199A1 JP 2010007027 W JP2010007027 W JP 2010007027W WO 2011074199 A1 WO2011074199 A1 WO 2011074199A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- charging
- voltage
- current
- secondary battery
- charge
- Prior art date
Links
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/42—Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells
- H01M10/44—Methods for charging or discharging
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/052—Li-accumulators
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
- H01M4/52—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
- H01M4/525—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
-
- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02J—CIRCUIT ARRANGEMENTS OR SYSTEMS FOR SUPPLYING OR DISTRIBUTING ELECTRIC POWER; SYSTEMS FOR STORING ELECTRIC ENERGY
- H02J7/00—Circuit arrangements for charging or depolarising batteries or for supplying loads from batteries
- H02J7/007—Regulation of charging or discharging current or voltage
- H02J7/0071—Regulation of charging or discharging current or voltage with a programmable schedule
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Definitions
- the present invention relates to a technique for shortening the charging time while suppressing deterioration of a nonaqueous electrolyte secondary battery.
- a lithium ion secondary battery is a kind of non-aqueous electrolyte secondary battery that uses a non-aqueous electrolyte as an electrolyte, and a negative electrode active material generally includes a carbon material that can occlude and release lithium. Used.
- a lithium-containing composite oxide LiCoO 2 or the like is used as the positive electrode active material.
- cycle characteristics In order to increase the capacity of the secondary battery, it is generally effective to increase the packing density of the active material.
- the packing density of the active material is increased, in the lithium ion secondary battery, the acceptability of the lithium ion of the active material is likely to be reduced during charging. As a result, the charge / discharge cycle life characteristics (hereinafter simply referred to as cycle characteristics) may deteriorate.
- the upper limit value of the charging voltage is high, the decomposition of the nonaqueous electrolyte is promoted, thereby reducing the cycle characteristics. Therefore, it is possible to prevent the cycle characteristics from being deteriorated by suppressing the upper limit value of the charging voltage.
- the charging current when the charging current is reduced, the amount of electricity that can be charged to the secondary battery per unit time is reduced, so that the charging time naturally becomes longer.
- the charging time of the secondary battery is required to be shortened in various fields. Therefore, if the charging current is simply reduced, the demand cannot be met.
- the upper limit value of the charging voltage is suppressed, the discharge capacity is reduced, and the time during which the device can be used by one charge is shortened.
- Patent Document 1 a lithium ion secondary battery is initially charged with a constant current at a high current, and when the terminal voltage of the battery reaches a predetermined cut-off voltage, the charging current is reduced to lower the battery voltage. At the same time, it has been proposed to switch the cut-off voltage after switching the current according to the voltage drop due to the internal resistance of the battery.
- Patent Document 2 a lithium ion secondary battery is charged at a constant current until the battery voltage reaches a specified voltage at a high current, and when the battery voltage reaches the specified voltage, the battery voltage is reduced by reducing the current. It is proposed to repeat the procedure of descending.
- Patent Document 1 when switching the charging current, the internal resistance of the battery is calculated, and the voltage drop corresponding to the internal resistance is added to the initial cutoff voltage (charging end voltage), so that the cutoff voltage is also calculated. Switching.
- the cut-off voltage when the cut-off voltage is set by the method of Patent Document 1, the cut-off voltage may become too high when the internal resistance of the battery increases. In such a case, the secondary battery is overcharged and the cycle characteristics are deteriorated.
- Patent Documents 1 and 2 in order to charge with a high current until a cutoff voltage that is substantially equal to the end-of-charge voltage or a specified voltage is reached, deterioration of the secondary battery may not be sufficiently suppressed. .
- the charging time tends to be long because the charging current is rapidly switched as the battery voltage drops.
- an object of the present invention is to provide an effective means for shortening the charging time of a nonaqueous electrolyte secondary battery.
- One aspect of the present invention is a method of charging a nonaqueous electrolyte secondary battery by repeating constant current charging and subsequent constant voltage charging n + 1 times, where n is an integer of 1 or more, (1) In the n-th charging, the secondary battery is charged to the voltage Ec (n) with the current Ic (n), and then the current is changed from Ic (n) to Ic (n +) with the voltage Ec (n). Charge the secondary battery until it decreases to 1), (2) In the (n + 1) th charge, the secondary battery is charged to the voltage Ec (n + 1) with the current Ic (n + 1), and then the current is Ic with the voltage Ec (n + 1).
- the present invention relates to a charging method for charging a secondary battery until it decreases from (n + 1) to Ic (n + 2).
- the multi-step charging is composed of three steps, for example, the first step constant voltage Ec (1) is 3.8 to 4.0 V, and the first step constant current Ic ( 1) is 0.7 to 2.0 It (0.7 to 2.0 C), the constant voltage Ec (2) of the second step is Ec (2)> Ec (1), and the second step is constant.
- the current Ic (2) is Ic (2) ⁇ Ic (1)
- the third step constant voltage Ec (3) is Ec (3)> Ec (2)
- the first step constant voltage Ec (1) is 3.8 to 4.0 V
- the first step constant current Ic (1) Is 0.7 to 2.0 It (0.7 to 2.0 C)
- the second step constant voltage Ec (2) is 4.0 to 4.4 V
- the second step constant current Ic (2 ) Is 0.3 to 0.7 It (0.3 to 0.7 C).
- Another aspect of the present invention includes at least one non-aqueous electrolyte secondary battery, a charging circuit that charges the secondary battery with electric power from an external power source, and a control that controls charging of the secondary battery by the charging circuit.
- a battery pack comprising: The control unit repeats constant current charging and subsequent constant voltage charging n + 1 times to charge the nonaqueous electrolyte secondary battery (where n is an integer of 1 or more), and (1) In the n-th charging, the secondary battery is charged to the voltage Ec (n) with the current Ic (n), and then the current is changed from Ic (n) to Ic (n +) with the voltage Ec (n).
- the present invention relates to a battery pack that controls the charging circuit such that a secondary battery is charged until it decreases from (n + 1) to Ic (n + 2).
- the charging time can be shortened without greatly impairing the charge / discharge cycle life characteristics of a non-aqueous electrolyte secondary battery typified by a lithium ion secondary battery.
- FIG. 1 is a functional block diagram of a battery pack to which a method for charging a lithium ion secondary battery according to an embodiment of the present invention is applied. It is a longitudinal cross-sectional view of an example of the lithium ion secondary battery contained in a battery pack same as the above. It is sectional drawing of the principal part of the positive electrode of a lithium ion secondary battery same as the above. It is a graph which shows the time change of the charging current of a charging process. It is a flowchart of a charging process.
- the present invention relates to a method for charging a nonaqueous electrolyte secondary battery by constant current-constant voltage charging.
- the non-aqueous electrolyte secondary battery is charged by repeating constant current charging and subsequent constant voltage charging n + 1 times. More specifically, (1) in the n-th charging, the secondary battery is charged to the voltage Ec (n) with the current Ic (n), and then the current is Ic (n) at the voltage Ec (n). ) To the secondary battery until it decreases from Ic (n + 1). (2) In the (n + 1) th charge, the secondary battery is charged to the voltage Ec (n + 1) with the current Ic (n + 1), and then the current is Ic with the voltage Ec (n + 1). The secondary battery is charged until it decreases from (n + 1) to Ic (n + 2).
- the upper limit voltage of constant current charging is switched stepwise to Ec (1), Ec (2),..., Ec (f) until reaching the end-of-charge voltage Ec (f).
- f is the maximum value of n and is an integer of 2 or more.
- a preferable value of f is 2 to 10, and 2 and 3 are particularly preferable.
- the constant current charging current Ic (n + 1) with the voltage Ec (n + 1) as the upper limit voltage is used, and the constant current charging current Ic (n) with the voltage Ec (n) as the upper limit voltage.
- the charging current decreases from the current Ic (n) to the current Ic (n + 1).
- the charging voltage reaches the charging end voltage Ec (f)
- constant voltage charging is performed at the charging end voltage Ec (f) until the charging current is reduced to a predetermined charging end current.
- the upper limit voltage for constant current charging is increased stepwise to the end-of-charge voltage Ec (f), and the charging current is decreased as the upper limit voltage increases.
- Ec (f) end-of-charge voltage
- the cycle characteristics refer to the relationship between the number of cycles and the discharge capacity when the secondary battery is repeatedly charged and discharged under a predetermined voltage range and under predetermined conditions.
- the number of cycles until the discharge capacity decreases from the initial capacity by a predetermined rate is also referred to as the cycle life of the secondary battery or simply as the life. It is said that the cycle characteristics deteriorate when the life of the secondary battery is shortened.
- the charging current when the charging current is switched, the charging current is switched by gradually decreasing the charging current instead of immediately decreasing the charging current.
- the average value of the charging current is increased, so that the charging time can be further shortened. Therefore, it is possible to further shorten the charging time while suppressing the deterioration of the cycle characteristics of the secondary battery.
- the positive electrode of the nonaqueous electrolyte secondary battery has the general formula: LiNi x Co y M 1- xy O 2 ( however, M is in the long period periodic table, Group 2 elements, Group III elements, Group 4 It is at least one element selected from the group consisting of an element, a group 7 element and a group 13 element, and preferably contains a material represented by 0.3 ⁇ x ⁇ 1, 0 ⁇ y ⁇ 0.4).
- a lithium ion secondary battery (hereinafter referred to as a Ni-based positive battery) using a lithium nickelate-based lithium-containing composite oxide (hereinafter referred to as a Ni-based positive electrode material) as a positive electrode active material is a lithium cobaltate lithium-containing composite.
- a lithium cobaltate lithium-containing composite Compared to lithium ion secondary batteries (hereinafter referred to as Co-based positive batteries) that use oxides (hereinafter referred to as Co-based positive electrode materials) as positive electrode active materials, the charging time when charging by constant current-constant voltage charging is shortened. Is easy. Note that, as x in the general formula increases, the positive electrode material approaches the Ni-based positive electrode material.
- the Ni-based positive electrode material has a lower potential than the Co-based positive electrode material when compared at the same charge depth.
- the Ni-based positive battery has a lower charging voltage profile than the Co-based positive battery. Therefore, even when batteries of the same capacity are charged with the same current, the time required for the charging voltage to reach the minimum target voltage is longer for Ni-based positive batteries than for Co-based positive batteries. As a result, the ratio of the constant current charging area to the entire charging can be increased.
- the Ni-based positive electrode battery charges a larger amount of electricity by constant current charging than the Co-based positive electrode battery. It is possible. Since constant current charging has a larger charging rate (charging current) than constant voltage charging, the charging time can be shortened by increasing the proportion of the constant current charging region in the entire charging.
- the Ni-based positive electrode battery can be charged in the same charging time as the Co-based positive electrode battery even if the charging current is reduced.
- the Ni-based positive electrode battery can improve the cycle characteristics even if the charging time is comparable to that of the Co-based positive electrode battery. Therefore, by setting the general formula of the lithium-containing composite oxide used for the positive electrode material as described above, it is possible to easily shorten the charging time while suppressing deterioration in cycle characteristics.
- the voltage Ec (1) is preferably a predetermined voltage in the range of 3.8 to 4V, and the constant current charging current Ic (1) with the voltage Ec (1) as the upper limit voltage is preferable.
- Is preferably a predetermined current in the range of 0.7 to 2C.
- the current of 1 C (1 It) is a current that can charge or discharge the amount of electricity corresponding to the nominal capacity of the secondary battery in one hour.
- the current of 0.7C is 0.7 times that of the current, and the current of 2C is twice that of the current.
- the current Ic (1) is the largest charging current in this method, and when the secondary battery is charged with a constant current with such a current Ic (1), the upper limit voltage is set to a voltage Ec (1) of 4 V or less. By setting, it can prevent that the lithium ion acceptance property of a negative electrode falls. Therefore, it is possible to prevent the cycle life from being shortened. On the other hand, by setting the voltage Ec (1) to 3.8 V or more, it is possible to prevent the charging time from becoming too long. From the above, by setting the voltage Ec (1) within the above range, it becomes easy to achieve both shortening the charging time and improving the cycle characteristics.
- a more preferable range of the current Ic (1) is 0.7 to 1.5C.
- the charge end voltage Ec (f) is 4 to 4.4 V
- the constant current charge current Ic (f) having the charge end voltage Ec (f) as the upper limit voltage is 0.3 to 0. .7C is preferred.
- the present invention includes at least one non-aqueous electrolyte secondary battery, a charging circuit that charges the secondary battery with power from an external power source, and a control unit that controls charging of the secondary battery by the charging circuit. Battery pack.
- the control unit controls the current and voltage of the charging circuit so as to charge the nonaqueous electrolyte secondary battery by repeating constant current charging and subsequent constant voltage charging n + 1 times.
- the control unit (1) charges the secondary battery up to the voltage Ec (n) with the current Ic (n) in the n-th charging, and then the voltage Ec (n). Then, the secondary battery is charged until the current decreases from Ic (n) to Ic (n + 1).
- the secondary battery In the (n + 1) th charge, the secondary battery is charged to the voltage Ec (n + 1) with the current Ic (n + 1), and then the current is Ic with the voltage Ec (n + 1).
- Control is performed so that the secondary battery is charged until it decreases from (n + 1) to Ic (n + 2).
- the voltage and current of the charging circuit are equal to the voltage for charging the secondary battery and the current for charging the secondary battery.
- FIG. 1 is a functional block diagram showing a battery pack to which a method for charging a lithium ion secondary battery according to Embodiment 1 of the present invention is applied.
- the battery pack 10 includes a secondary battery 12, a charging circuit 14, a discharging circuit 15, a voltage sensor 16 that detects the voltage of the secondary battery 12, a current sensor 17 that detects a charging current and a discharging current of the secondary battery 12, and two A control unit 18 that controls charging and discharging of the secondary battery 12 is included.
- the battery pack 10 can be connected to the load device 20 and the external power supply 22. When the secondary battery 12 is charged, the secondary battery 12 and the charging circuit 14 are connected, and when the secondary battery 12 is discharged, the secondary battery 12 and the discharging circuit 15 are connected.
- the secondary battery 12 of the battery pack 10 may be a single lithium ion secondary battery or an assembled battery in which a plurality of lithium ion secondary batteries are connected in parallel and / or in series.
- the control unit 18 may be provided with a part of the control function of the control unit 18 described later in the load device 20 or may be provided in a charger or the like for charging the battery pack 10.
- the secondary battery 12 is connected to the load device 20 via the discharge circuit 15 and connected to an external power source 22 such as a commercial power source via the charging circuit 14. Detection values of the voltage sensor 16 and the current sensor 17 are sent to the control unit 18.
- the load device 20 has a wiring that receives power supply only from the secondary battery 12 in order to simplify the description.
- the present invention is not limited to this, and includes a case where power is supplied from the external power supply 22 to the load device 20 while charging the secondary battery 12. In that case, the secondary battery 12 (charging circuit 14) and the load device 20 are connected in parallel to the external power source 22 during charging.
- the control unit 18 controls the charging circuit 14 and the discharging circuit 15 so as to maintain the voltage of the secondary battery 12 at a voltage within a predetermined range.
- a control unit can be composed of a microcomputer, a CPU (Central Processnng Unnt), an MPU (Mncro Processnng Unnt), a main storage device, an auxiliary storage device, and the like.
- auxiliary storage device nonvolatile memory or the like
- information on a plurality of upper limit voltages when the secondary battery 12 is charged with constant current information on charge currents corresponding to the respective upper limit voltages, charge end voltage and charge Information on the cutoff current, information on the discharge cutoff voltage, and the like are stored.
- the lithium ion secondary battery 24 in the illustrated example has a cylindrical shape
- the present invention is not limited to this and is applied to lithium ion secondary batteries having various shapes such as a square shape, a flat shape, and a pin shape. be able to.
- the lithium ion secondary battery 24 includes an electrode group 31 formed by spirally winding a positive electrode 26, a negative electrode 28, and a separator 30 interposed therebetween.
- the electrode group 31 is housed in a bottomed cylindrical metal case 32 having an opening together with a non-aqueous electrolyte (not shown). Inside the case 32, an upper insulating plate 36 and a lower insulating plate 38 are disposed on the upper and lower sides of the electrode group 31, respectively.
- the opening of the case 32 is sealed by the assembly sealing plate 34, and the electrode group 31 and the nonaqueous electrolyte are thereby sealed inside the case 32.
- the assembly sealing plate 34 is placed on a small diameter portion 46 provided on the upper portion of the case 32 in a state where the assembly sealing plate 34 is electrically insulated from the case 32 by an insulating gasket 44. In this state, the assembly sealing plate 34 is crimped by crimping the opening end of the case 32 so that the peripheral edge of the assembly sealing plate 34 is sandwiched between the small diameter portion 46 and the opening end from above the gasket 44. Attach to the opening of the case 32.
- the assembly sealing plate 34 is connected to the positive electrode 26 via the positive electrode lead 40. Thereby, the assembly sealing plate 34 functions as an external terminal of the positive electrode 26.
- the negative electrode 28 is connected to the case 32 via a negative electrode lead 48. Thereby, the case 32 functions as an external terminal of the negative electrode 28.
- the positive electrode 26 includes a positive electrode current collector 26a made of, for example, aluminum foil, and a positive electrode active material layer 26b formed on at least one surface of the positive electrode current collector 26a.
- the positive electrode active material layer 26b is made of a mixture of a positive electrode active material, a conductive material, and a binder.
- the positive electrode active material the general formula: LiNi x Co y M 1- xy O 2 (where, M is in the long period periodic table, Group 2 elements, Group III elements, Group 4 elements, Group 7 elements and 13
- a lithium-containing composite oxide which is at least one element selected from the group consisting of group elements and is represented by 0.3 ⁇ x ⁇ 1.0, 0 ⁇ y ⁇ 0.4).
- x is preferably 0.6 ⁇ x ⁇ 0.9
- y is preferably 0.05 ⁇ y ⁇ 0.2.
- M When x is 0.3 or more, the effect of reducing the charging voltage by using the Ni-based positive electrode material is remarkably obtained. Similarly, when y is less than 0.4, the effect of reducing the charging voltage is remarkably obtained.
- group 2 elements include Mg and Ca.
- Group 3 elements include Sc and Y.
- group 4 elements include Ti and Zr.
- An example of a Group 7 element is Mn.
- group 13 elements include B and Al. Among these, M is most preferably Al in terms of excellent stability of the crystal structure and ensuring safety.
- a carbon material such as natural graphite, artificial graphite, carbon black, or acetylene black can be used.
- binder polyvinylidene fluoride (PVDF) or polytetrafluoroethylene (PTFE) can be used.
- PVDF polyvinylidene fluoride
- PTFE polytetrafluoroethylene
- a metal foil such as an aluminum foil can be used for the positive electrode current collector.
- the positive electrode is obtained by applying a positive electrode paste obtained by dispersing a mixture of a positive electrode active material, a conductive material, and a binder in a dispersion medium such as N-methyl-2-pyrrolidone on a positive electrode current collector. It can be obtained by drying.
- the negative electrode 28 also includes a negative electrode current collector and a negative electrode active material layer formed on the negative electrode current collector.
- the negative electrode active material layer may be a deposited film formed by vapor deposition or the like, or may be a mixture of a negative electrode active material, a conductive material, and a binder.
- a carbon material capable of inserting and extracting lithium, artificial graphite, or natural graphite can be used. Silicon alloys and silicon oxides can also be used.
- a metal foil such as a nickel foil or a copper foil can be used for the negative electrode current collector.
- the conductive material and the binder the same materials as the positive electrode can be used.
- a negative electrode paste obtained by dispersing a mixture of a negative electrode active material, a conductive material, and a binder in a dispersion medium such as N-methyl-2-pyrrolidone was applied on the negative electrode current collector. Thereafter, it can be obtained by drying.
- the electrolytic solution includes a non-aqueous solvent and a supporting salt that dissolves in the non-aqueous solvent.
- a lithium salt such as lithium hexafluorophosphate (LiPF 6 ) can be used as the supporting salt.
- cyclic esters such as ethylene carbonate (EC) and propylene carbonate (PC) with chain esters such as dimethyl carbonate (DMC), diethyl carbonate (DEC), and methyl ethyl carbonate (MEC)
- DMC dimethyl carbonate
- DEC diethyl carbonate
- MEC methyl ethyl carbonate
- the charging process executed by the control unit 18 will be described.
- the secondary battery 12 is charged by alternately executing constant current charging and constant voltage charging. That is, the constant current charging in a plurality of steps is executed by switching the upper limit voltage and the charging current step by step. And constant voltage charge is performed after the constant current charge of each step.
- the voltage value of the upper limit voltage for constant current charging at each step is expressed as Ec (n).
- n 1, 2,..., F (f is an integer equal to or greater than 2), and Ec (1) ⁇ Ec (2) ⁇ ... ⁇ Ec (f).
- the constant current charging current whose upper limit voltage is the voltage Ec (n) is represented by Ic (n).
- the highest voltage Ec (f) among the upper limit voltages is the charge end voltage.
- FIG. 4 is an example of charge switching in the above charging process, and here, the current of constant current charging is switched to three stages of Ic (1), Ic (2), and Ic (f).
- Ic (e) is a charge termination current.
- the number of steps of constant current charging according to the present invention is not limited to three steps as shown in FIG. 4, and can be set to an arbitrary number of steps of two or more steps.
- FIG. 5 is a flowchart of processing executed by, for example, the CPU of the control unit.
- the process of FIG. 5 is repeatedly executed at predetermined time intervals.
- step S1 when charging of the secondary battery 12 is started, a value “1” is substituted for the variable n (step S1), and the voltage E of the secondary battery 12 is detected by the voltage sensor 16 (step S2).
- step S3 the voltage E and the voltage Ec (n) are compared to determine whether E is smaller than Ec (n) (step S3).
- Ec (1) is preferably a voltage in the range of 3.8 to 4V.
- the voltage E a value calculated by detecting the voltage of the secondary battery 12 every predetermined time (for example, 25 ms) and moving average thereof can be used.
- the current Ic (1) is preferably a current in the range of 0.7 to 2C. If E is equal to or greater than Ec (n) (No in step S3), the process proceeds to step S8 described later.
- Step S5 When the secondary battery 12 is charged at a constant current with the current Ic (n), the voltage E and the voltage Ec (n) are compared to determine whether E is equal to or greater than Ec (n) (step S5). . If E is less than Ec (n) (No in Step S5), Step S5 is repeatedly executed until the voltage E becomes equal to or higher than the voltage Ec (n) (Yes in Step S5).
- step S7 it is determined whether or not the current I detected by the current sensor 17 during the constant voltage charging is equal to or less than Ic (n + 1) (step S7). If the current I is larger than Ic (n + 1) (No in step S7), this step S7 is repeated until the current I decreases below Ic (n + 1). If the current I is equal to or less than Ic (n + 1) (Yes in step S7), the value “1” is added to the variable n (step S8), and the variable n that is the addition result is the value “f”. Is reached (step S9).
- the constant current charging current Ic (f) when the voltage is the charge end voltage Ec (f) is read. Thereby, the secondary battery 12 is charged with a constant current with the current Ic (f) (step S10).
- Step S11 the voltage E and the voltage Ec (f) are compared to determine whether E is equal to or greater than Ec (f) (step S11). If E is less than Ec (f) (No in Step S11), Step S11 is repeatedly executed until the voltage E becomes equal to or higher than the voltage Ec (f) (Yes in Step S11).
- step S11 If voltage E is equal to or higher than voltage Ec (f) (Yes in step S11), the charging mode is switched from constant current charging to constant voltage charging, and constant voltage charging is performed with voltage Ec (f) (step S12).
- the charge end current Ic (e) is read out from the information on the charge current.
- step S13 it is determined whether or not the current I detected by the current sensor 17 during the constant voltage charging is equal to or less than Ic (e) (step S13). If the current I is larger than Ic (e) (No in step S13), this step S13 is repeated until the current I decreases below Ic (e). If the current I is equal to or less than Ic (e) (Yes in step S13), the charging is stopped (step S14), and the process is terminated.
- Example 1 A cylindrical lithium ion secondary battery shown in FIG. 2 used in the charging method of the present invention was produced by the following procedure.
- the positive electrode paste was applied to both surfaces of a positive electrode current collector made of an aluminum foil having a thickness of 15 ⁇ m and dried to form a positive electrode active material layer on both surfaces of the positive electrode current collector. In this way, a plate-like positive electrode was obtained. Thereafter, this positive electrode was rolled and cut to obtain a belt-like positive electrode (thickness 0.110 mm, width 57 mm, length 720 mm).
- LiPF 6 was dissolved at a concentration of 1 mol / L in a non-aqueous solvent in which EC, MEC, and DMC were mixed at a volume ratio of 1: 1: 8 to obtain a non-aqueous electrolyte.
- the negative electrode lead pulled out from the negative electrode was welded to the inner bottom surface of the case.
- the positive electrode lead pulled out from the positive electrode was welded to the lower surface of the assembly sealing plate.
- the opening end of the case was caulked to the peripheral edge of the assembly sealing plate via a gasket to seal the opening of the case. In this way, a 18650 size cylindrical lithium ion secondary battery for test (diameter: 18 mm, height: 65 mm, nominal capacity: 1800 mAh) was produced.
- Example 2 The charge / discharge treatment was repeated 300 cycles in the same manner as in Example 1 except that LiCoO 2 was used as the positive electrode active material and the discharge end voltage was set to 3V.
- Comparative Example 2 The charge / discharge treatment was repeated 300 cycles in the same manner as in Comparative Example 1 except that LiCoO 2 was used as the positive electrode active material and the discharge end voltage was set to 3V.
- Example 3 The charge / discharge treatment was repeated 300 cycles in the same manner as in Example 1 except that the upper limit voltage of the first step was set to 3.8V.
- Comparative Example 3 The charge / discharge treatment was repeated 300 cycles in the same manner as in Comparative Example 1 except that the upper limit voltage of the first step was set to 3.8V.
- Example 4 The charge / discharge treatment was repeated 300 cycles in the same manner as in Example 1 except that the current (Ic (1)) in the first step constant current charging was set to 2C.
- Comparative Example 4 The charge / discharge treatment was repeated 300 cycles in the same manner as in Comparative Example 1 except that the current (Ic (1)) in the constant current charging in the first step was set to 2C.
- Example 5 The charge / discharge process was repeated 300 cycles in the same manner as in Example 1 except that the lower limit current in constant voltage charging in the first step was set to 0.3 C (Ic (2)) and the second step was omitted. .
- Example 6 The charge / discharge treatment was repeated 300 cycles in the same manner as in Example 5 except that LiCoO 2 was used as the positive electrode active material and the upper limit voltage of constant current charging in the third step was set to 4.4V.
- Comparative Example 6 The charge / discharge treatment was repeated 300 cycles in the same manner as in Comparative Example 5 except that LiCoO 2 was used as the positive electrode active material and the upper limit voltage of constant current charging in the third step was set to 4.4V.
- Example 1 Comparing Example 1 in which the charging current is gradually reduced when switching the charging current with Comparative Example 1 in which the charging current is switched immediately, only the charging time is shortened without reducing the capacity maintenance rate. I understand that. This is the result of comparison between Example 2 and Comparative Example 2, Example 3 and Comparative Example 3, Example 4 and Comparative Example 4, Example 5 and Comparative Example 5, and Example 6 and Comparative Example 6, respectively. The same applies to.
- the present invention basically charges a lithium ion secondary battery by high rate charging in a constant voltage region where the charging depth is small, and charges a lithium ion secondary battery by low rate charging in a high voltage region where the charging depth is large. By doing so, the life of the lithium ion secondary battery is extended. The charging time is shortened by gradually switching the charging current. According to the results of the respective examples and the corresponding comparative examples, it can be seen that the present invention can achieve both shortening of the charging time and improvement of the cycle characteristics.
- the third embodiment has an initial charge time because the upper limit voltage of the constant current charging in the first step, which is high rate charging, is lower than that of the first embodiment. It is longer than 1. On the other hand, the capacity maintenance rate is further improved. In Example 4 in which the current of constant voltage charging in the first step is 2C, the capacity retention rate is lower than in other examples. In Examples 5 and 6 in which the second step is omitted, the charging time is slightly longer.
- Example 6 where the charge end voltage is 4.4V, the initial charge time is longer than in Example 1 where the charge end voltage is 4.2V. However, as the end-of-charge voltage increases, the discharge capacity increases accordingly, and it is natural that the charging time increases accordingly. On the other hand, the capacity retention rate of Example 6 is 69%, which is a sufficiently acceptable result.
- the charging method of the present invention can be suitably used as a power source for electronic devices such as portable devices and information devices because the lifetime of the nonaqueous electrolyte secondary battery can be extended and the charging time can be shortened.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Inorganic Chemistry (AREA)
- Power Engineering (AREA)
- Secondary Cells (AREA)
- Charge And Discharge Circuits For Batteries Or The Like (AREA)
- Battery Electrode And Active Subsutance (AREA)
- Battery Mounting, Suspending (AREA)
Abstract
Description
(1)n回目の充電は、電流Ic(n)で、電圧Ec(n)まで二次電池を充電し、続いて、電圧Ec(n)で、電流がIc(n)からIc(n+1)に減少するまで二次電池を充電し、
(2)(n+1)回目の充電は、電流Ic(n+1)で、電圧Ec(n+1)まで二次電池を充電し、続いて、電圧Ec(n+1)で、電流がIc(n+1)からIc(n+2)に減少するまで二次電池を充電する、充電方法に関する。
前記制御部が、定電流充電と、それに続く定電圧充電とをn+1回繰り返して非水電解質二次電池を充電し(ただし、nは1以上の整数)、かつ、
(1)n回目の充電は、電流Ic(n)で、電圧Ec(n)まで二次電池を充電し、続いて、電圧Ec(n)で、電流がIc(n)からIc(n+1)に減少するまで二次電池を充電し、
(2)(n+1)回目の充電は、電流Ic(n+1)で、電圧Ec(n+1)まで二次電池を充電し、続いて、電圧Ec(n+1)で、電流がIc(n+1)からIc(n+2)に減少するまで二次電池を充電する、ように、前記充電回路を制御する、電池パックに関する。
(実施形態1)
図1に、本発明の実施形態1に係るリチウムイオン二次電池の充電方法が適用される、電池パックを機能ブロック図により示す。
下記手順により本発明の充電方法に用いられる、図2に示す円筒形リチウムイオン二次電池を作製した。
正極活物質としてのLiNi0.8Co0.15Al0.05O2の100重量部と、結着剤としてのPVDFの1.7重量部と、導電材としてのアセチレンブラックの2.5重量部と、適量のN-メチル-2-ピロリドンとを、双腕式練合機にて攪拌し、正極ペーストを得た。
負極活物質としての黒鉛100重量部と、結着剤としてのPVDF0.6重量部と、増粘剤としてのカルボキシメチルセルロース1重量部と、適量の水とを、双腕式練合機にて攪拌し、負極ペーストを得た。この負極ペーストを厚み8μmの銅箔からなる負極集電体の両面に塗布し、乾燥して、負極集電体の両面に負極活物質層を形成した。このようにして、プレート状の負極を得た。その後、この負極を圧延及び裁断して、帯状の負極(厚み0.130mm、幅58.5mm、長さ800mm)を得た。
ECと、MECと、DMCとを体積比1:1:8の割合で混合した非水溶媒に、LiPF6を1mol/Lの濃度で溶解して非水電解質を調製した。
上記で得られた正極及び負極と、両電極を隔離するセパレータとを渦巻き状に巻回して電極群を構成した。セパレータには、厚み20μmのポリプロピレン製の微多孔膜を用いた。この電極群をケース(直径:18mm、高さ:65mm)内に挿入した。このとき、電極群の上部及び下部にそれぞれ絶縁部材を配した。上記で得られた非水電解質をケース内に注入した。
上述の試験用のリチウムイオン二次電池を、上限電圧を4V(Ec(1))に設定して、0.7Cの電流(Ic(1))で、定電流充電(CC充電)した。充電電圧が4Vに達すると、その電圧で、下限電流を0.5C(Ic(2))として、上記二次電池を定電圧充電(CV充電)した。
次に、上記二次電池を、上限電圧を4.1V(Ec(2))に設定して、上記0.5Cの電流(Ic(2))で、定電流充電した。充電電圧が4.1Vに達すると、その電圧で、下限電流を0.3C(Ic(f))として、上記二次電池を定電圧充電した。
次に、上記二次電池を、上限電圧を4.2Vの充電終止電圧(Ec(f))に設定して、上記0.3Cの電流(Ic(f))で、定電流充電した。充電電圧が4.2Vに達すると、その電圧で、充電電流が充電終止電流50mAに減少するまで、上記二次電池を定電圧充電した。
第1ステップ及び第2ステップで、定電圧充電を行わず、充電電流を、直ちに0.7C(Ic(1))から0.5C(Ic(2))に切り替えたこと、並びに、直ちに0.5C(Ic(2))から0.3C(Ic(f))に切り替えたこと、以外は実施例1と同様にして、充放電処理を300サイクル繰り返した。
正極活物質にLiCoO2を使用するとともに、放電終止電圧を3Vに設定したこと以外は実施例1と同様にして、充放電処理を300サイクル繰り返した。
正極活物質にLiCoO2を使用するとともに、放電終止電圧を3Vに設定したこと以外は比較例1と同様にして、充放電処理を300サイクル繰り返した。
第1ステップの上限電圧を3.8Vに設定したこと以外は実施例1と同様にして、充放電処理を300サイクル繰り返した。
第1ステップの上限電圧を3.8Vに設定したこと以外は比較例1と同様にして、充放電処理を300サイクル繰り返した。
第1ステップの定電流充電における電流(Ic(1))を2Cに設定したこと以外は実施例1と同様にして、充放電処理を300サイクル繰り返した。
第1ステップの定電流充電における電流(Ic(1))を2Cに設定したこと以外は比較例1と同様にして、充放電処理を300サイクル繰り返した。
第1ステップの定電圧充電における下限電流を0.3C(Ic(2))に設定するとともに、第2ステップを省略したこと以外は実施例1と同様にして、充放電処理を300サイクル繰り返した。
第2ステップを省略したこと以外は比較例1と同様にして、充放電処理を300サイクル繰り返した。
正極活物質にLiCoO2を使用するとともに、第3ステップの定電流充電の上限電圧を4.4Vに設定したこと以外は実施例5と同様にして、充放電処理を300サイクル繰り返した。
正極活物質にLiCoO2を使用するとともに、第3ステップの定電流充電の上限電圧を4.4Vに設定したこと以外は比較例5と同様にして、充放電処理を300サイクル繰り返した。
容量維持率(%)=300サイクル目の放電容量/1サイクル目の放電容量×100 (1)
12 二次電池
14 充電回路
16 電圧センサ
17 電流センサ
18 制御部
Claims (5)
- 定電流充電と、それに続く定電圧充電とをn+1回繰り返して非水電解質二次電池を充電する方法、ただし、nは1以上の整数、であって、
(1)n回目の充電は、電流Ic(n)で、電圧Ec(n)まで二次電池を充電し、続いて、電圧Ec(n)で、電流がIc(n)からIc(n+1)に減少するまで二次電池を充電し、
(2)(n+1)回目の充電は、電流Ic(n+1)で、電圧Ec(n+1)まで二次電池を充電し、続いて、電圧Ec(n+1)で、電流がIc(n+1)からIc(n+2)に減少するまで二次電池を充電する、充電方法。 - 前記非水電解質二次電池が、正極、負極及び非水電解質を具備し、
前記正極が、一般式:LiNixCoyM1-x-yO2(ただし、Mは、長周期型周期表における、2族元素、3族元素、4族元素、7族元素及び13族元素からなる群より選択される少なくとも1つの元素であり、0.3≦x<1、0<y<0.4)で表される材料を含む、請求項1記載の非水電解質二次電池の充電方法。 - 電圧Ec(1)が3.8~4Vであり、電流Ic(1)が、0.7~2Cの電流である、請求項1または2記載の非水電解質二次電池の充電方法。
- 充電終止電圧Ec(f)(ただし、fは、nの最大値であり、かつ2以上の整数)が4~4.4Vであり、電流Ic(f)が、0.3~0.7Cの電流である、請求項3記載の非水電解質二次電池の充電方法。
- 少なくとも1つの非水電解質二次電池と、前記二次電池を外部電源からの電力により充電する充電回路と、前記充電回路による前記二次電池の充電を制御する制御部とを具備した電池パックであって、
前記制御部が、定電流充電と、それに続く定電圧充電とをn+1回繰り返して非水電解質二次電池を充電し(ただし、nは1以上の整数)、かつ、
(1)n回目の充電は、電流Ic(n)で、電圧Ec(n)まで二次電池を充電し、続いて、電圧Ec(n)で、電流がIc(n)からIc(n+1)に減少するまで二次電池を充電し、
(2)(n+1)回目の充電は、電流Ic(n+1)で、電圧Ec(n+1)まで二次電池を充電し、続いて、電圧Ec(n+1)で、電流がIc(n+1)からIc(n+2)に減少するまで二次電池を充電する、ように、前記充電回路を制御する、電池パック。
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201080025120.7A CN102473969B (zh) | 2009-12-14 | 2010-12-02 | 非水电解质二次电池的充电方法及电池包 |
US13/388,636 US8912762B2 (en) | 2009-12-14 | 2010-12-02 | Charging method for non-aqueous electrolyte secondary battery by repeating a set of constant current charge and constant voltage charge and battery pack implementing the charging method |
JP2011526732A JP4818491B2 (ja) | 2009-12-14 | 2010-12-02 | 非水電解質二次電池の充電方法、及び電池パック |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2009282511 | 2009-12-14 | ||
JP2009-282511 | 2009-12-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2011074199A1 true WO2011074199A1 (ja) | 2011-06-23 |
Family
ID=44166974
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2010/007027 WO2011074199A1 (ja) | 2009-12-14 | 2010-12-02 | 非水電解質二次電池の充電方法、及び電池パック |
Country Status (4)
Country | Link |
---|---|
US (1) | US8912762B2 (ja) |
JP (1) | JP4818491B2 (ja) |
CN (1) | CN102473969B (ja) |
WO (1) | WO2011074199A1 (ja) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012127775A1 (ja) * | 2011-03-18 | 2012-09-27 | パナソニック株式会社 | 非水電解質二次電池の充電方法、及び電池パック |
JP2013045590A (ja) * | 2011-08-23 | 2013-03-04 | Shin Etsu Chem Co Ltd | 非水電解質二次電池の充電方法及び非水電解質二次電池 |
WO2013046690A1 (ja) * | 2011-09-30 | 2013-04-04 | パナソニック株式会社 | リチウムイオン電池の充電方法及び電池搭載機器 |
JP2014164801A (ja) * | 2013-02-21 | 2014-09-08 | Shin Kobe Electric Mach Co Ltd | 非水電解液、それを用いた非水電解液二次電池、および該非水電解液二次電池を用いた二次電池システム |
JPWO2019167493A1 (ja) * | 2018-02-28 | 2021-03-11 | パナソニックIpマネジメント株式会社 | 非水電解質二次電池の充電方法、及び非水電解質二次電池の充電システム |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103427125B (zh) * | 2012-05-15 | 2016-04-13 | 清华大学 | 硫基聚合物锂离子电池的循环方法 |
US9728995B2 (en) * | 2015-04-08 | 2017-08-08 | Intel Corporation | Systems, methods and devices for adaptable battery charging |
KR102285148B1 (ko) * | 2016-08-22 | 2021-08-04 | 삼성에스디아이 주식회사 | 배터리 충전 방법 및 이를 이용하는 배터리 충전 장치 |
TWI625915B (zh) * | 2016-11-18 | 2018-06-01 | Industrial Technology Research Institute | 智慧型充電方法 |
KR102254353B1 (ko) * | 2017-03-10 | 2021-05-21 | 주식회사 엘지화학 | 이차전지의 충전방법 |
CN107204493B (zh) | 2017-04-28 | 2020-09-29 | 宁德时代新能源科技股份有限公司 | 电池充电方法、装置和设备 |
KR102544462B1 (ko) * | 2018-01-25 | 2023-06-19 | 삼성전자 주식회사 | 배터리를 포함하는 전자 장치 및 이의 충전구간을 제어하는 방법 |
WO2019227419A1 (zh) * | 2018-05-31 | 2019-12-05 | Oppo广东移动通信有限公司 | 充电方法和充电装置 |
KR20200099416A (ko) * | 2019-02-14 | 2020-08-24 | 삼성전자주식회사 | 배터리를 충전하는 방법 및 그 방법을 적용한 전자 장치 |
CN112768795A (zh) * | 2019-11-06 | 2021-05-07 | 北京小米移动软件有限公司 | 一种电池充电方法、装置及介质 |
CN111509803A (zh) * | 2020-04-26 | 2020-08-07 | 深圳润丰新能源有限公司 | 一种阶梯式锂电池充电控制方法 |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09121462A (ja) * | 1995-10-24 | 1997-05-06 | Matsushita Electric Ind Co Ltd | 定電流・定電圧充電装置 |
JPH09289741A (ja) * | 1996-04-19 | 1997-11-04 | Suzuki Motor Corp | 充電器 |
JP2003333706A (ja) * | 2002-05-10 | 2003-11-21 | Sumitomonacco Materials Handling Co Ltd | 車両用バッテリ充電装置およびバッテリ充電システム |
JP2007228701A (ja) * | 2006-02-22 | 2007-09-06 | Sharp Corp | 携帯端末装置 |
JP2008130278A (ja) * | 2006-11-17 | 2008-06-05 | Matsushita Electric Ind Co Ltd | 充電システム、充電装置、及び電池パック |
JP2008167642A (ja) * | 2006-12-04 | 2008-07-17 | Matsushita Electric Ind Co Ltd | 充電システム、充電装置、及び電池パック |
JP2009022078A (ja) * | 2007-07-10 | 2009-01-29 | Sanyo Electric Co Ltd | リチウムイオン二次電池の充電方法 |
JP2009033843A (ja) * | 2007-07-26 | 2009-02-12 | Panasonic Electric Works Co Ltd | 充電装置および充電方法 |
JP2009290931A (ja) * | 2008-05-27 | 2009-12-10 | Kyocera Corp | 充電回路 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3692547B2 (ja) | 1994-04-22 | 2005-09-07 | ソニー株式会社 | 充電方法 |
JP3884802B2 (ja) | 1996-11-07 | 2007-02-21 | 日産自動車株式会社 | リチウムイオン電池の充電方法 |
US6081097A (en) * | 1998-01-19 | 2000-06-27 | Matsushita Electric Industrial Co., Ltd. | Method for charging lithium secondary battery |
JP2005085566A (ja) * | 2003-09-08 | 2005-03-31 | Sanyo Electric Co Ltd | 非水電解質二次電池の充放電制御方法 |
US8013577B2 (en) | 2006-12-04 | 2011-09-06 | Panasonic Corporation | Charging system, charging apparatus and battery pack |
KR20110022556A (ko) * | 2008-06-12 | 2011-03-07 | 파나소닉 주식회사 | 리튬 이온 이차전지의 충전 방법 및 충방전 방법 |
JP5077386B2 (ja) * | 2010-04-28 | 2012-11-21 | ソニー株式会社 | 充電制御方法および電池パック |
-
2010
- 2010-12-02 WO PCT/JP2010/007027 patent/WO2011074199A1/ja active Application Filing
- 2010-12-02 US US13/388,636 patent/US8912762B2/en active Active
- 2010-12-02 CN CN201080025120.7A patent/CN102473969B/zh active Active
- 2010-12-02 JP JP2011526732A patent/JP4818491B2/ja active Active
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09121462A (ja) * | 1995-10-24 | 1997-05-06 | Matsushita Electric Ind Co Ltd | 定電流・定電圧充電装置 |
JPH09289741A (ja) * | 1996-04-19 | 1997-11-04 | Suzuki Motor Corp | 充電器 |
JP2003333706A (ja) * | 2002-05-10 | 2003-11-21 | Sumitomonacco Materials Handling Co Ltd | 車両用バッテリ充電装置およびバッテリ充電システム |
JP2007228701A (ja) * | 2006-02-22 | 2007-09-06 | Sharp Corp | 携帯端末装置 |
JP2008130278A (ja) * | 2006-11-17 | 2008-06-05 | Matsushita Electric Ind Co Ltd | 充電システム、充電装置、及び電池パック |
JP2008167642A (ja) * | 2006-12-04 | 2008-07-17 | Matsushita Electric Ind Co Ltd | 充電システム、充電装置、及び電池パック |
JP2009022078A (ja) * | 2007-07-10 | 2009-01-29 | Sanyo Electric Co Ltd | リチウムイオン二次電池の充電方法 |
JP2009033843A (ja) * | 2007-07-26 | 2009-02-12 | Panasonic Electric Works Co Ltd | 充電装置および充電方法 |
JP2009290931A (ja) * | 2008-05-27 | 2009-12-10 | Kyocera Corp | 充電回路 |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012127775A1 (ja) * | 2011-03-18 | 2012-09-27 | パナソニック株式会社 | 非水電解質二次電池の充電方法、及び電池パック |
JP5089825B2 (ja) * | 2011-03-18 | 2012-12-05 | パナソニック株式会社 | 非水電解質二次電池の充電方法、及び電池パック |
US9246344B2 (en) | 2011-03-18 | 2016-01-26 | Panasonic Intellectual Property Management Co., Ltd. | Charging method for non-aqueous electrolyte secondary battery, and battery pack |
JP2013045590A (ja) * | 2011-08-23 | 2013-03-04 | Shin Etsu Chem Co Ltd | 非水電解質二次電池の充電方法及び非水電解質二次電池 |
WO2013046690A1 (ja) * | 2011-09-30 | 2013-04-04 | パナソニック株式会社 | リチウムイオン電池の充電方法及び電池搭載機器 |
JPWO2013046690A1 (ja) * | 2011-09-30 | 2015-03-26 | パナソニックIpマネジメント株式会社 | リチウムイオン電池の充電方法及び電池搭載機器 |
US9368995B2 (en) | 2011-09-30 | 2016-06-14 | Panasonic Intellectual Property Management Co., Ltd. | Lithium ion battery charging method and battery-equipped device |
JP2014164801A (ja) * | 2013-02-21 | 2014-09-08 | Shin Kobe Electric Mach Co Ltd | 非水電解液、それを用いた非水電解液二次電池、および該非水電解液二次電池を用いた二次電池システム |
JPWO2019167493A1 (ja) * | 2018-02-28 | 2021-03-11 | パナソニックIpマネジメント株式会社 | 非水電解質二次電池の充電方法、及び非水電解質二次電池の充電システム |
US11949091B2 (en) | 2018-02-28 | 2024-04-02 | Panasonic Intellectual Property Management Co., Ltd. | Charging method of non-aqueous electrolyte secondary battery, and charging system of non-aqueous electrolyte secondary battery |
Also Published As
Publication number | Publication date |
---|---|
US20120133338A1 (en) | 2012-05-31 |
US8912762B2 (en) | 2014-12-16 |
JP4818491B2 (ja) | 2011-11-16 |
CN102473969B (zh) | 2014-07-02 |
CN102473969A (zh) | 2012-05-23 |
JPWO2011074199A1 (ja) | 2013-04-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP4818491B2 (ja) | 非水電解質二次電池の充電方法、及び電池パック | |
JP5089825B2 (ja) | 非水電解質二次電池の充電方法、及び電池パック | |
WO2011065009A1 (ja) | リチウムイオン二次電池の充電方法、及び電池パック | |
WO2009150773A1 (ja) | リチウムイオン二次電池の充電方法および充放電方法 | |
EP2905831B1 (en) | Cathode additive for high-capacity lithium secondary battery | |
KR101222220B1 (ko) | 비수 전해질 이차전지의 충전방법 및 충전장치 | |
US9368995B2 (en) | Lithium ion battery charging method and battery-equipped device | |
US9065292B2 (en) | Methods and systems for charging electrochemical cells | |
KR100802851B1 (ko) | 비수 전해액 이차전지 | |
KR20170100526A (ko) | 리튬 이온 이차 전지의 충전 방법 및 그 충전 제어 시스템, 및 그 충전 제어 시스템을 구비한 전자기기 및 전지 팩 | |
JPH07296853A (ja) | 充電方法 | |
JP2008262827A (ja) | コイン形非水電解液二次電池 | |
JP2012124026A (ja) | 非水電解液二次電池 | |
KR101520118B1 (ko) | 리튬이차전지의 사이클 성능 개선 방법 | |
JP5122899B2 (ja) | 放電制御装置 | |
JP2012252951A (ja) | 非水電解質二次電池 | |
JP2009158142A (ja) | 非水電解質二次電池の充電方法 | |
JP2013131426A (ja) | 非水電解質二次電池の充電方法、及び電池パック | |
JP2010086862A (ja) | 組電池パック及び組電池パックの製造方法 | |
JP2001052760A (ja) | 非水電解液二次電池の充電方法 | |
JP2004227931A (ja) | 非水電解質二次電池 | |
JP2008300178A (ja) | 非水二次電池 | |
CN106605330B (zh) | 非水电解质二次电池的控制方法 | |
JP2012209026A (ja) | 組電池の製造方法 | |
KR101676404B1 (ko) | 리튬 이차전지용 음극 활물질 및 이를 포함한 리튬 이차전지 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 201080025120.7 Country of ref document: CN |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2011526732 Country of ref document: JP |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 10837236 Country of ref document: EP Kind code of ref document: A1 |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 10837236 Country of ref document: EP Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 13388636 Country of ref document: US |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 10837236 Country of ref document: EP Kind code of ref document: A1 |