Method for reproducing negative electrode active material

Abstract

To provide a reproducing method for obtaining a negative electrode active material having improved rapid charge / discharge characteristics from a used lithium ion secondary battery.SOLUTION: A method for reproducing a negative electrode active material from a used lithium ion secondary battery includes a preparation step S10 for preparing a used lithium ion secondary battery 1 including a positive electrode 30, a negative electrode 40 including a negative electrode active material containing a carbon material, and an electrolyte, a charging step S20 for charging the lithium ion secondary battery 1, a discharging step S30 for discharging the lithium ion secondary battery 1 after the charging step S20, the discharging being performed at a discharge rate higher than the charge rate of the charging step S20, and a recovery step S40 for recovering the negative electrode active material containing the carbon material from the negative electrode 40 for the lithium ion secondary battery 1 after the discharging step S30.SELECTED DRAWING: Figure 3

Description

[Technical field]

[0001] The present disclosure relates to a method for regenerating negative electrode active materials. [Background technology]

[0002] Secondary batteries are suitably used in various applications, including as driving power sources mounted on vehicles such as hybrid electric vehicles (HEVs), plug-in hybrid electric vehicles (PHEVs), and electric vehicles (BEVs), and the demand for secondary batteries is rapidly expanding. In response to such demand, there is also an increasing demand for technology related to the reproduction of negative electrode active materials from used lithium-ion secondary batteries. For example, Patent Document 1 discloses a technology related to the reproduction of negative electrode active materials, in which a negative electrode is removed from a lithium-ion secondary battery, the negative electrode is washed with a liquid containing water, the negative electrode is separated into a negative electrode mixture containing a negative electrode active material and a binder, and a current collecting substrate, and then the negative electrode mixture is mixed with a solvent capable of dissolving or dispersing the binder to prepare a negative electrode paste, which is then applied onto a negative electrode current collector. [Prior art documents] [Patent documents]

[0003] [Patent Document 1] JP 2006-228509 A Summary of the Invention [Problem to be solved by the invention]

[0004] In the case of negative electrode active materials, not only is there a need for technology related to the reproduction of negative electrode active materials, but there is also a need for improved performance of the reproduced negative electrode active materials, for example, improved rapid charge / discharge characteristics. In the case of negative electrode active materials recovered by conventional techniques such as those disclosed in Patent Document 1, no consideration is given to rapid charge / discharge characteristics. Therefore, the demand for rapid charge / discharge characteristics as described above cannot be fully met.

[0005] The technology disclosed herein has been made in consideration of the above circumstances, and relates to a remanufacturing method for obtaining a negative electrode active material with improved rapid charge / discharge characteristics from a used lithium ion secondary battery. [Means for solving the problem]

[0006] The technology disclosed herein is a method for reproducing a negative electrode active material from a used lithium ion secondary battery, and includes a preparation step of preparing a used lithium ion secondary battery comprising a positive electrode, a negative electrode comprising a negative electrode active material containing a carbon material, and an electrolyte; a charging step of charging the lithium ion secondary battery; a discharging step of discharging the lithium ion secondary battery after the charging step, the discharging step comprising discharging at a discharge rate higher than the charge rate of the charging step; and a recovery step of recovering the negative electrode active material containing a carbon material from the negative electrode of the lithium ion secondary battery after the discharging step.

[0007] According to this configuration, by discharging the lithium ion secondary battery at a discharge rate higher than the charge rate, the surface layer of the negative electrode active material of the negative electrode becomes amorphous, and the rapid charge / discharge characteristics of the negative electrode active material are improved, so that the negative electrode active material with improved rapid charge / discharge characteristics can be reproduced. [Brief description of the drawings]

[0008] [Figure 1] FIG. 1 is a vertical cross-sectional view that illustrates a schematic internal structure of a lithium-ion secondary battery according to one embodiment. [Diagram 2] FIG. 2 is a perspective view that typically shows an electrode assembly of the lithium ion secondary battery shown in FIG. [Diagram 3] FIG. 3 is a flowchart illustrating a reproduction method according to one embodiment. [Figure 4] FIG. 4 is a flow chart illustrating a sub-step of the recovery step according to one embodiment. [Diagram 5] FIG. 5 is a partially enlarged view that illustrates a schematic view of the surface layer of a negative electrode active material (carbon material) and the state of lithium ions according to one embodiment. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0009] Hereinafter, embodiments of the technology disclosed herein will be described with reference to the drawings. Note that matters other than those specifically mentioned in this specification and necessary for implementing the technology disclosed herein can be understood as design matters for a person skilled in the art based on the prior art in the field. The technology disclosed herein can be implemented based on the contents disclosed in this specification and the technical common sense in the field.

[0010] In the following drawings, the same reference numerals are used for components and parts that perform the same function, and duplicated descriptions may be omitted or simplified. In the present specification, the expression "A to B" indicating a range includes the meanings of "preferably larger than A" and "preferably smaller than B" as well as A or more and B or less. In the present specification, the term "secondary battery" refers to a repeatedly chargeable and dischargeable power storage device, and includes so-called storage batteries and power storage elements such as electric double layer capacitors. In the present specification, the term "lithium ion secondary battery" refers to a secondary battery that uses lithium ions as a charge carrier and realizes charging and discharging by the transfer of charge associated with lithium ions between positive and negative electrodes.

[0011] 1. Preparation target In the method for reproducing the negative electrode active material according to the present embodiment, a specified lithium ion secondary battery is prepared, and the negative electrode active material is reproduced. An example of the preparation subject here is a used lithium ion secondary battery. This lithium ion secondary battery will be specifically described below. FIG. 1 is a vertical cross-sectional view that typically shows the internal structure of a lithium ion secondary battery. FIG. 2 is a perspective view that typically shows an electrode body of the lithium ion secondary battery shown in FIG. 1. As shown in FIG. 1, the lithium ion secondary battery 1 includes a case 10, an electrode body 20, and an electrolyte (not shown).

[0012] (1) Case The case 10 is a box-shaped container. An electrode body 20 and an electrolyte are accommodated inside the case 10. For example, a metal material (such as aluminum (Al)) having a certain strength is used for the case 10. A liquid injection hole 16 may be provided in the case 10. The liquid injection hole 16 is a hole for injecting the electrolyte. After the electrolyte is injected, the liquid injection hole 16 is sealed by a sealing member 18. In addition, a positive electrode terminal 12 and a negative electrode terminal 14 are attached to the case 10. The positive electrode terminal 12 and the negative electrode terminal 14 are connected to the electrode body 20 inside the case 10. Specifically, the positive electrode terminal 12 is connected to the positive electrode 30 (see FIG. 2) of the electrode body 20. The positive electrode terminal 12 is made of aluminum (Al) or the like. On the other hand, the negative electrode terminal 14 is connected to the negative electrode 40 of the electrode body 20. The negative electrode terminal 14 is made of copper (Cu) or the like.

[0013] (2) Electrode body The electrode body 20 is a power generating element of the lithium ion secondary battery 1. As shown in Fig. 2, the electrode body 20 includes a positive electrode 30, a negative electrode 40, and a separator 50. The electrode body 20 shown in Fig. 2 is a wound electrode body. This wound electrode body is produced by laminating the positive electrode 30, the negative electrode 40, and the separator 50 to form a long strip-shaped laminate, and then winding the laminate. However, the structure of the electrode body 20 is not particularly limited, and may be any other conventionally known structure (such as a laminated electrode body).

[0014] The positive electrode 30 includes a positive electrode core 32, which is a metal foil having electrical conductivity, and a positive electrode active material layer 34 applied to the surface of the positive electrode core 32. Aluminum (Al) or the like is used for the positive electrode core 32. The positive electrode active material layer 34 is a composite layer containing a positive electrode active material, a conductive material, a binder, and the like. The positive electrode active material is a particulate material that can reversibly absorb and release charge carriers. Examples of the positive electrode active material include lithium nickel composite oxides (e.g., LiNiO2, etc.), lithium cobalt composite oxides (e.g., LiCoO2, etc.), lithium nickel cobalt manganese composite oxides (e.g., LiNi 1 / 3 Co 1 / 3 Mn 1 / 3O2, etc.), lithium nickel cobalt aluminum composite oxides (e.g., LiNi 0.8 Co 0.15 Al 0.5 O2, etc.), lithium manganese composite oxides (e.g., LiMn2O4, etc.), lithium nickel manganese composite oxides (e.g., LiNi 0.5 Mn 1.5 Examples of the conductive material include carbon materials such as acetylene black and graphite. Examples of the binder include resin materials such as polyvinylidene fluoride (PVdF).

[0015] The negative electrode 40 includes a negative electrode core 42, which is a metal foil having electrical conductivity, and a negative electrode active material layer 44 applied to the surface of the negative electrode core 42. The negative electrode core 42 is made of copper (Cu) or the like. The negative electrode active material layer 44 is a composite layer containing a negative electrode active material, a binder, a thickener, and the like. The negative electrode active material is a particulate material capable of reversibly absorbing and releasing charge carriers. The negative electrode active material to be prepared essentially contains a carbon material. Examples of the carbon material include graphite, hard carbon, and soft carbon, and among these, graphite is preferably used. The graphite may be natural graphite or artificial graphite. In addition to the above carbon materials, lithium titanate (LTO), silicon carbide, a composite containing carbon and silicon (Si-C composite), silicon oxide (SiO X ) may be included. Although not particularly limited, from the viewpoint of remanufacturing efficiency, the ratio of the carbon material is preferably 50% by mass or more when the entire negative electrode active material is taken as 100% by mass. Examples of the binder include resin materials such as styrene butadiene rubber (SBR). Examples of the thickener include resin materials such as carboxymethyl cellulose (CMC).

[0016] In some preferred embodiments, the positive and negative electrode capacity ratio of the lithium ion secondary battery 1 is preferably 1.0 or more. This makes it possible to more suitably reproduce the negative electrode active material with excellent rapid charge and discharge performance. The positive and negative electrode capacity ratio is preferably 1.0 or more, more preferably 1.05 or more, more preferably 1.2 or more, and even more preferably 1.5 or more. When the positive and negative electrode capacity ratio is closer to 1.0, the utilization rate of the negative electrode active material is increased, so that the surface of the negative electrode active material can be suitably amorphized, and a negative electrode active material with excellent rapid charge and discharge performance can be obtained. In addition, when the positive and negative electrode capacity ratio is below 1.0 (less than 1.0), metallic lithium is precipitated on the negative electrode, which may cause a short circuit, so that the positive and negative electrode capacity ratio is preferably 1.0 or more. The upper limit of the positive and negative electrode capacity ratio is not particularly limited, but is preferably 2.2 or less, more preferably 2.0 or less, more preferably 1.9 or less, and even more preferably 1.7 or less. In this specification, the "positive and negative electrode capacity ratio" can be calculated by separately calculating the positive electrode capacity and the negative electrode capacity, and the positive and negative electrode capacity ratio can be calculated by the following formula: positive and negative electrode capacity ratio = negative electrode capacity / positive electrode capacity. Here, the positive and negative electrode capacity ratio can be easily adjusted, for example, by changing the basis weight of the positive and negative electrodes or by changing the type of the positive and negative electrode active material. The "basis weight" refers to the value obtained by dividing the mass of the electrode active material layer by the area of ​​the formation region (mass of the electrode active material layer / area of ​​the formation region). In addition, the positive electrode capacity can be calculated as the capacity (i.e., the initial positive electrode charge capacity) when a half cell is prepared with Li metal as the counter electrode and initially charged in a voltage range corresponding to the full cell (for example, about 2 to 4.2 V). The negative electrode capacity can be calculated, for example, by adding up the initial negative electrode discharge capacity and the use voltage range of the negative electrode.

[0017] The separator 50 is an insulating sheet interposed between the positive electrode 30 and the negative electrode 40. For example, a resin material such as polyethylene (PE), polypropylene (PP), polyester, cellulose, or polyamide is used for the separator 50. A heat-resistant layer containing an inorganic filler may be formed on the surface of the separator 50. Examples of such inorganic fillers include inorganic oxides such as aluminum oxide, magnesium oxide, silicon oxide, and titanium oxide; nitrides such as aluminum nitride and silicon nitride; metal hydroxides such as calcium hydroxide, magnesium hydroxide, and aluminum hydroxide; and clay minerals such as mica, talc, boehmite, zeolite, apatite, and kaolin.

[0018] (3) Electrolyte The electrolyte exists between the positive electrode 30 and the negative electrode 40. This allows charge carriers to move between the positive electrode 30 and the negative electrode 40. Examples of the electrolyte include non-aqueous electrolytes and gel electrolytes. The electrolyte can be any electrolyte that can be used in conventional lithium ion secondary batteries without any particular limitations. The electrolyte typically includes a solvent and a supporting salt. As the solvent, various non-aqueous solvents used in this type of lithium ion secondary battery, for example, carbonate-based non-aqueous solvents such as ethylene carbonate (EC), diethyl carbonate (DEC), dimethyl carbonate (DMC), and ethyl methyl carbonate (EMC), are used. As the supporting salt, for example, lithium salts such as LiPF6, LiBF4, and lithium bis(fluorosulfonyl)imide (LiFSI) can be suitably used. The concentration of the supporting salt is not particularly limited, but is preferably about 0.7 mol / L or more and 1.3 mol / L or less. The electrolyte may contain components other than the above-mentioned solvent and supporting salt, so long as the effect of the present technology is not significantly impaired, and may contain various additives such as a gas generating agent, a film forming agent, a dispersing agent, a thickener, etc. Examples of additives used in the nonaqueous electrolyte 80 include positive and negative electrode film forming agents such as vinylene carbonate (VC), fluoroethylene carbonate (FEC), 1,3-propane sultone (PS), etc.; overcharge inhibitors such as biphenyl (BP), cyclohexylbenzene (CHB), t-butylbenzene, t-amylbenzene, etc.

[0019] The lithium ion secondary battery 1 has been described above as an example of a preparation target for the remanufacturing method according to the present embodiment. However, the remanufacturing method disclosed herein is not limited to a method in which the lithium ion secondary battery 1 having the above configuration is prepared. In other words, the lithium ion secondary battery prepared for the remanufacturing method disclosed herein may include a positive electrode, a negative electrode, and an electrolyte, and is not particularly limited to a specific structure.

[0020] 2. Method for reproducing negative electrode active material Hereinafter, the method for reproducing the negative electrode active material according to the present embodiment will be described. Fig. 3 is a flowchart for explaining the method for reproducing according to one embodiment. Fig. 4 is a flowchart for explaining a sub-step of the recovery step S40 according to one embodiment.

[0021] As shown in Fig. 3, the method for reproducing a negative electrode active material according to the first embodiment includes a preparation step S10, a charging step S20, a discharging step S30, and a recovery step S40. The reproducing method disclosed herein may further include other steps at any stage, and the other processes may be the same as those of the conventional method. Each step will be described below.

[0022] (1) Preparation process S10 In the preparation step S10, a lithium ion secondary battery for reproducing the negative electrode active material is prepared. The lithium ion secondary battery prepared here includes a positive electrode, a negative electrode having a negative electrode active material containing a carbon material, and an electrolyte. The details of the lithium ion secondary battery have already been described, so duplicated descriptions will be omitted.

[0023] (2) Charging process S20 In the charging step S20, the lithium ion secondary battery prepared in the preparation step S10 is charged. The charging step S20 is characterized in that the lithium ion secondary battery is charged at a charge rate that is relatively lower than the discharge rate in the discharging step S30.

[0024] In some preferred embodiments, it is preferable to perform the charging step S20 at a charging rate of 0.5C or less. This allows the negative electrode active material with excellent rapid charge / discharge performance to be reproduced. The charging rate of the charging step S20 is preferably 0.5C or less, more preferably 0.3C or less, and even more preferably 0.2C or less. The charging rate of the charging step S20 is not particularly limited, but is, for example, 0.01C or more, and preferably 0.1C or more.

[0025] In some preferred embodiments, in the charging step S20, it is preferable to charge the lithium ion secondary battery 1 until the state of charge (SOC) is 50% or more. This allows the anode active material with excellent rapid charge / discharge performance to be reproduced. It is more preferable to charge the lithium ion secondary battery 1 until the SOC is 80% or more, and even more preferable to charge until the SOC is 100% (rated voltage). The higher the SOC in the charging step S20, the more widely the lithium ions diffuse into the layer of the anode active material, so that the surface of the anode active material can be more suitably amorphized. That is, it is possible to suitably reproduce the anode active material with excellent rapid charge / discharge performance. Also, charging may be performed once, or may be repeated two or more times, for example, with a discharge in between.

[0026] The temperature when the charging step S20 is performed is not particularly limited, but is, for example, 100° C. or lower, and preferably 80° C. or lower. The temperature when the charging step S20 is performed is not particularly limited, but is, for example, 0° C. or higher, preferably 40° C. or higher, and more preferably 50° C. or higher.

[0027] (3) Discharge process S30 In the discharging step S30, the lithium ion secondary battery that has been through the charging step S20 is charged. Here, the discharging step S30 is characterized in that the lithium ion secondary battery is discharged at a discharge rate higher than the charge rate in the charging step S20.

[0028] Fig. 5 is a partially enlarged view showing a schematic view of the surface layer of the negative electrode active material 46 and the lithium ions 60 according to one embodiment. Fig. 5(A) shows the state before the charging step S20 is performed. Fig. 5(B) and Fig. 5(C) show the state during the charging step S20. Fig. 5(D) shows the state during the discharging step S30. For ease of explanation, the behavior of the lithium ions 60 is illustrated by hollow arrows in Figs. 5(B) to (D). In FIG. 5, the negative electrode active material 46 is a carbon material. Before the charging step S20, the lithium ions 60 are typically stabilized in the electrolyte in a state where the solvent molecules 62 constituting the electrolyte are coordinated (solvation) (see FIG. 5(A)). Here, as shown in FIG. 5(B), the lithium ion 60 in the electrolyte is inserted between the layers of the surface layer of the negative electrode active material 46 by performing the charging step S20 on the lithium ion secondary battery 1. As shown in FIG. 5(C), the inserted lithium ions 60 are released from the solvent molecules 62 (desolvation) as the charging step S20 progresses, and are diffused into the layers of the negative electrode active material 46. This expands the gap between the layers of the negative electrode active material 46. Then, by performing the discharging step S30 with a discharge rate relatively higher than the charge rate of the charging step S20, the lithium ions 60 inserted between the layers of the negative electrode active material 46 are released again to the outside of the negative electrode active material 46 as shown in FIG. 5(D). The charging step S20 and the discharging step S30 cause the surface layer of the negative electrode active material 46, in which lithium ions 60 have been inserted and extracted, to become amorphous (see FIG. 5(D)). The amorphous nature of the surface layer of the negative electrode active material 46 improves the rapid charge / discharge performance of the negative electrode active material 46. Then, the recovery step S40, which will be described later, allows the recovery of the negative electrode active material 46 with improved rapid charge / discharge performance.

[0029] In some preferred embodiments, it is preferable to perform the discharge step S30 at a discharge rate of 0.5C or more. The discharge rate of the discharge step S30 is preferably 0.5C or more, more preferably 0.8C or more, and even more preferably 1.0C or more. This makes it possible to reproduce a negative electrode active material with excellent rapid charge / discharge performance. The discharge rate of the discharge step S30 is not particularly limited, but is 20C or less, preferably 10C or less.

[0030] In some preferred embodiments, in the discharging step S30, it is preferable to discharge the lithium ion secondary battery 1 until its state of charge (SOC) is 30% or less. It is more preferable to discharge the lithium ion secondary battery 1 until its SOC is 20% or less, more preferably 10% or less, more preferably 5% or less, and even more preferably 0%. Discharging may be performed once, or may be repeated two or more times, for example, with charging in between.

[0031] The difference between the discharge rate and the charge rate (discharge rate-charge rate) is preferably 0.4C or more, preferably 0.7C or more, preferably 0.8C or more, preferably 0.9C or more, and more preferably 3.9C or more. The larger the difference between the discharge rate and the charge rate, the more favorably the anode active material surface can be amorphized. Therefore, anode active material with excellent rapid charge / discharge performance can be reproduced. The upper limit of the difference between the discharge rate and the charge rate (discharge rate-charge rate) is not particularly limited, but may be, for example, 10C or less.

[0032] (4) Recovery process S40 In the recovery step S40, the negative electrode active material is recovered from the lithium ion secondary battery that has been through the charging step S20 and the discharging step S30. The method for recovering the negative electrode active material in the recovery step S40 is not particularly limited since it can use a conventionally known technique. The recovery step S40 may include sub-steps, such as a roasting step S41, a sorting step S43, an acid treatment step S45, and a magnetic sorting step S47, as shown in FIG. 4. The following is a detailed description.

[0033] (4-1) Roasting process S41 In the roasting step S41, the lithium ion secondary battery is roasted at a predetermined temperature. This removes liquid components (electrolyte, etc.) from the object to be recovered and carbonizes resin components (binder, separator, etc.). In addition, by carrying out the roasting step S41, the function of the battery can be stopped. As the method of the roasting step S41 can be any technique used in conventional recovery techniques without particular limitations, and does not characterize the technique disclosed herein, detailed description will be omitted.

[0034] (4-2) Sorting process S43 In the sorting step S43, each member included in the lithium ion secondary battery 1 is sorted. The sorting step S43 may be carried out by a conventionally known method, for example, by using a sieve or by visual inspection.

[0035] In addition, in the sorting step S43, a crushing process may be performed on the lithium ion secondary battery 1 as necessary. This makes it possible to obtain crushed lithium ion secondary batteries 1, and improves the efficiency of sorting each component. For example, when the lithium ion secondary battery 1 is to be collected, it is preferable to crush the case 10 and the electrode body 20. This makes it easier to remove the case 10, the negative electrode core 42, and the positive electrode 30 from the lithium ion secondary battery 1.

[0036] Although not limited thereto, the crushed material of the lithium ion secondary battery 1 obtained by the above-mentioned crushing process is sorted using a sieve. In this case, typically, metal components (Al, Cu, etc.) derived mainly from the case 10, the positive electrode core 32, and the negative electrode core 42 remain as coarse particles on the sieve, and black mass from which most of the metal components (Al, Cu, etc.) have been removed is obtained as fine particles below the sieve. The black mass typically contains a negative electrode active material and a positive electrode active material (e.g., Ni, Co, etc.).

[0037] In addition, in the sorting step S43, the sorted black mass can be further sorted by a flotation method. This makes it possible to remove most of the components (e.g., Ni, Co, etc.) other than the negative electrode active material in the black mass. As the flotation method, any known technique such as a multi-oil flotation method, a water surface flotation method, or a foam flotation method can be used without any particular restrictions.

[0038] (4-3) Acid treatment step S45 In the acid treatment step S45, the black mass obtained in the sorting step S43 is mixed with an acid solution. As a result, metal elements (Al, Cu, Ni, Co, etc.) in the black mass are dissolved in the acid solution, while the negative electrode active material is not dissolved in the acid solution and remains as a residue. Depending on the configuration of the object to be recovered and the composition of the acid solution, some metal elements (Fe, etc.) in the black mass may not be dissolved in the acid solution and remain as a residue. That is, the residue obtained in the acid treatment step S45 may contain, for example, Fe, in addition to the negative electrode active material. In this case, the metal elements in the residue can be removed, for example, by the magnetic sorting step S47 described later. The procedure of the acid treatment step S45 can be a conventionally known procedure without any particular restrictions. As an example, the pH of the acid solution used in the acid treatment step S45 is preferably -1.5 to 1.5 (more preferably -0.5 to 0.5). This allows the metal components in the black mass to be suitably dissolved. Specific examples of the acid solution include inorganic acids such as sulfuric acid, nitric acid, hydrochloric acid, and phosphoric acid, and organic acids such as citric acid, ascorbic acid, oxalic acid, and acetic acid. In addition to the acid solution, a reducing agent such as hydrogen peroxide can be added in the acid treatment step S45, but this is not limited thereto. This allows the metal elements in the black mass to dissolve in the acid solution, and the treatment time for the acid treatment step S45 can be shortened.

[0039] The acid solution after the acid treatment step S45 and the residue are subjected to solid-liquid separation by filtration or the like, thereby obtaining a residue containing a negative electrode active material. The method of solid-liquid separation can be any conventionally known means without particular limitation. The acid solution after solid-liquid separation can be, but is not limited to, recovered from the acid solution by, for example, a conventionally known treatment method to recover metal elements (Ni, Co, etc.) in the acid solution.

[0040] (4-4) Magnetic sorting process S47 In the magnetic sorting step S47, the residue obtained in the acid treatment step S45 is sorted by magnetic force. This makes it possible to separate the negative electrode active material as a non-magnetic material in the residue from the magnetic material (metallic components). That is, the negative electrode active material according to the present embodiment can be obtained by the magnetic sorting step S47. In the magnetic sorting step S47, a conventionally known procedure can be adopted without particular limitation.

[0041] The method for reproducing the negative electrode active material according to the present embodiment has been described above. As described above, the method for reproducing the negative electrode active material according to the present embodiment includes the preparation step S10, the charging step S20, the discharging step S30, and the recovery step S40, and it is possible to obtain a negative electrode active material in which the surface of the negative electrode active material (hereinafter, referred to as the "active material substrate") to be prepared is amorphous. Therefore, the method for reproducing the negative electrode active material according to the present embodiment can obtain a negative electrode active material with excellent rapid charge / discharge characteristics.

[0042] 3. Recovered negative electrode active material (negative electrode active material obtained in recovery step S40) The negative electrode active material obtained by the method for reproducing a negative electrode active material according to this embodiment (hereinafter also referred to as "recovered negative electrode active material") is a prepared negative electrode active material whose surface has been amorphized by the charging step S20 and the discharging step S30, as described above. That is, it has characteristics different from the negative electrode active material contained in the lithium ion secondary battery 1 prepared in the preparation step S10. The characteristics of the recovered negative electrode active material will be described below.

[0043] The recovered negative electrode active material corresponds to the carbon material among the negative electrode active materials to be prepared. In other words, the recovered negative electrode active material is a carbon material whose surface has been made amorphous by the charging step S20 and the discharging step S30. The recovered negative electrode active material is a particulate material that can reversibly store and release charge carriers. Typically, a carbon material such as graphite, hard carbon, or soft carbon is used as the active material substrate. The graphite may be natural graphite or artificial graphite.

[0044] As an example of an index relating to the surface properties of the recovered negative electrode active material according to this embodiment, the G band intensity (I G ) versus D band intensity (I D ) ratio (I D / I G ) can be mentioned. D / I G The ratio is average information showing the crystallinity at a depth of nano-order from the surface of the negative electrode active material. G ) versus D band intensity (I D ) ratio (I D / I G The "Raman spectrum" can be measured using a known Raman spectrometer as follows. Specifically, the Raman spectrum of the negative electrode active material is measured using a laser with a wavelength of 532 nm. -1 The peak intensity near the D band intensity (I D ), 1590cm -1 The peak intensity near the G band intensity (I G ), and I D / I G It can be found by calculating the value of

[0045] In some preferred embodiments, the G band intensity (I G ) versus D band intensity (I D ) ratio (I D / I G) is preferably 0.38 or more. G ) is a typical indicator of a regular graphite structure, and the D band intensity (I D ) is an index that typically indicates an irregular graphite structure. That is, the I D / I G It can be said that the larger the ratio, the more favorably the surface of the recovered negative electrode active material is amorphous. D / I G The larger the ratio, the higher the lithium ion acceptance capacity. In other words, the discharge capacity of the recovered negative electrode active material is improved, and the rapid charge / discharge performance is good. D / I G The ratio is preferably 0.38 or more, more preferably 0.40 or more, more preferably 0.42 or more, and even more preferably 0.47 or more. D / I G The upper limit of the ratio is not particularly limited, but may be, for example, 1.0 or less.

[0046] Another example of an index relating to the surface properties of the recovered negative electrode active material according to this embodiment is the interlayer distance d(002) of the recovered negative electrode active material based on X-ray diffraction (XRD). The interlayer distance d(002) of the negative electrode active material is average information indicating the crystallinity at a depth of the order of microns from the surface of the negative electrode active material. Note that the "interlayer distance d(002) of the negative electrode active material" in this specification can be measured by a commercially available X-ray diffraction device using a CuKα radiation source according to a known method.

[0047] In some preferred embodiments, the interlayer distance d(002) of the recovered negative electrode active material based on X-ray diffraction (XRD) is preferably 3.350 Å or more and 3.369 Å or less. In the recovered negative electrode active material in this embodiment, the surface of the negative electrode active material is amorphous by passing through the above-mentioned charging step S20 and discharging step S30, so that when recovered as a recovered negative electrode active material, the interlayer distance d(002) becomes smaller. The smaller the interlayer distance d(002) of the recovered negative electrode active material, the more favorably the surface of the recovered negative electrode active material is amorphous, and the easier it is to insert or remove lithium ions from the negative electrode active material, so that the rapid charge / discharge performance is good. The interlayer distance d(002) of the recovered negative electrode active material is preferably 3.369 Å or less, more preferably 3.361 Å or less, and even more preferably 3.359 Å or less. The interlayer distance d(002) of the recovered negative electrode active material is preferably 3.350 Å or more.

[0048] The average particle diameter (median diameter: D50) of the recovered negative electrode active material is not particularly limited, but is, for example, 0.1 μm to 50 μm, preferably 1 μm to 25 μm. The average particle diameter (D50) of the recovered negative electrode active material can be determined, for example, by a laser diffraction scattering method.

[0049] An embodiment of the technology disclosed herein has been described above. Note that the technology disclosed herein is not limited to the above embodiment, and includes other embodiments with various modifications.

[0050] <Applications of negative electrode active materials> The negative electrode active material (recovered negative electrode active material) obtained by the remanufacturing method according to this embodiment can be used as, for example, a negative electrode active material of a secondary battery, although it is not limited thereto. A secondary battery including the negative electrode active material obtained by the remanufacturing method according to this embodiment can be used for various applications, and can be suitably used as, for example, a power source (driving power source) for a motor mounted on a vehicle such as a passenger car or truck. The type of vehicle is not particularly limited, and examples thereof include a plug-in hybrid vehicle (PHEV), a hybrid vehicle (HEV), and an electric vehicle (BEV; Battery Electric Vehicle). The secondary battery can also be suitably used as a battery pack in which a plurality of secondary batteries are arranged in a predetermined arrangement direction and a load is applied from the arrangement direction by a restraining mechanism. The shape of the secondary battery is not limited to a square shape, and may be a coin type, a button type, a cylindrical type, or the like. It can also be configured as a secondary battery including a laminated case.

[0051] Hereinafter, examples of the technology disclosed herein will be described, but it is not intended that the technology disclosed herein be limited to those shown in these examples.

[0052] <Study 1: Study of charging and discharging conditions> [Preparation of lithium-ion secondary batteries] (Example 1) First, a used lithium ion secondary battery was prepared in which an electrode assembly including a positive electrode, a negative electrode, and a separator, and an electrolyte were housed inside a case. The positive electrode is made of aluminum and has a positive electrode active material, LiNi 1 / 3 Co 1 / 3 Mn 1 / 3 A positive electrode active material layer containing O2 (lithium nickel cobalt manganese composite oxide) was provided. The negative electrode was prepared by providing a negative electrode active material layer containing natural graphite as a negative electrode active material on the surface of a copper negative electrode core. The electrolyte was prepared by dissolving LiPF6 as a supporting salt in a mixed solvent containing ethylene carbonate (EC), dimethyl carbonate (DMC), and ethyl methyl carbonate (EMC) in a volume ratio of EC:DMC:EMC = 30:30:40 to a concentration of 1 mol / L.

[0053] [Charging process] The lithium ion secondary battery prepared above was subjected to constant current constant voltage (CCCV) charging at a charge rate of 0.1 C in a temperature environment of 25° C. until the SOC at the end of charging reached 100%.

[0054] [Discharge process] The lithium ion secondary battery that had been subjected to the charging process described above was subjected to constant current constant voltage (CCCV) discharge at a discharge rate of 1C in a temperature environment of 25°C until the SOC at the end of discharge reached 10%.

[0055] [Recovery of negative electrode active material] The lithium ion secondary battery that had been subjected to the above-mentioned discharge step was disassembled, and the negative electrode was taken out. The negative electrode active material layer was peeled off from the negative electrode by washing with water. The negative electrode active material was recovered from the negative electrode active material layer, and the moisture was removed by drying at 100°C. In this way, the powdered negative electrode active material was recovered.

[0056] (Example 2 to Example 4) In Examples 2 to 4, lithium ion secondary batteries having the same configuration as in Example 1 were prepared, and a charging step was performed at the charging rate shown in Table 1. Otherwise, the charging step and discharging step were performed under the same conditions as in Example 1, and the negative electrode active materials according to Examples 2 to 4 were recovered.

[0057] (Example 5 to Example 6) In Examples 5 and 6, lithium ion secondary batteries having the same configuration as in Example 1 were prepared, and a charging process was performed until the SOC at the end of charging reached the value shown in Table 1. Otherwise, the charging process and discharging process were performed under the same conditions as in Example 1, and the negative electrode active materials according to Examples 5 and 6 were recovered.

[0058] (Examples 7 to 10) In Examples 7 to 10, lithium ion secondary batteries having the same configuration as in Example 1 were prepared, and a discharging step was performed at the discharge rate shown in Table 1. Otherwise, the charging step and discharging step were performed under the same conditions as in Example 1, and the negative electrode active materials according to Examples 7 to 10 were recovered.

[0059] (Example 11 to Example 14) In Examples 11 to 14, lithium ion secondary batteries having the same configuration as in Example 1 were prepared, and a discharging process was performed until the SOC at the end of discharge reached the value shown in Table 1. Otherwise, the charging process and discharging process were performed under the same conditions as in Example 1, and the negative electrode active materials according to Examples 11 to 14 were recovered.

[0060] (Example 15) In Example 15, a lithium ion secondary battery having the same configuration as in Example 1 was prepared. In Example 15, the charging and discharging steps were not performed, and the negative electrode active material was recovered as it was. The rest of the procedure was the same as in Example 1.

[0061] [Evaluation of interlayer distance d(002) of recovered negative electrode active material] The recovered negative electrode active materials according to Examples 1 to 15 (hereinafter also referred to as "recovered negative electrode active materials") were evaluated. First, the interlayer distance d(002) of the recovered negative electrode active materials was evaluated by X-ray diffraction (XRD). Specifically, XRD measurement was performed on the recovered negative electrode active material particles under the following conditions. The results are shown in Table 1. Measurement device: Smart Lab (Rigaku Corporation) Measurement method: Wide angle method Radiation source: CuKα radiation Measurement range: 5~90° Voltage: 45kV Current: 200mA

[0062] [Raman peak intensity ratio of recovered negative electrode active material (I D / I G ) Evaluation Next, the Raman peak intensity ratio (I D / I GSpecifically, a commercially available laser microscopic Raman analyzer (manufactured by Thermo Fisher Scientific) was used to obtain a Raman spectrum under the following conditions. -1 The peak intensity of I D , 1570cm -1 The peak intensity of I G , the Raman peak intensity ratio (I D / I G The above-mentioned Raman spectrum measurement was carried out 10 times (n=10), and the average value was calculated. The results are shown in Table 1. Objective lens: 50x Laser wavelength: 532nm Laser output: 1mV

[0063] [Preparation of evaluation coin cells] In order to evaluate the performance of the recovered negative electrode active material, a coin cell was prepared as a single-electrode cell in which a negative electrode as a working electrode and metallic lithium as a counter electrode were opposed to each other. First, a negative electrode was prepared using the recovered negative electrode active material. Specifically, the recovered negative electrode active material, styrene butadiene rubber (SBR) as a binder, and carboxymethyl cellulose (CMC) as a thickener were mixed with ion-exchanged water as a solvent so that the mass ratio of the solid content was recovered negative electrode active material:SBR:CMC=98:1:1 to prepare a negative electrode paste. The negative electrode paste was applied to one side of a long sheet-shaped copper foil (thickness 10 μm) as a negative electrode core (negative electrode current collector), dried, and pressed with a roll press machine to prepare a sheet-shaped negative electrode. The sheet-shaped negative electrode was punched out to the size of a coin cell, and the weight (g) of the negative electrode after punching was measured. The weight of the negative electrode core was subtracted from the weight of the negative electrode, and the result was multiplied by 0.98 (the ratio of the recovered negative electrode active material to the entire negative electrode active material layer) to obtain the weight (g) of the negative electrode active material.

[0064] The separator used was a 24 μm-thick porous polyolefin sheet with a three-layer structure of PP / PE / PP, with a ceramic layer (4 μm thick) containing alumina (Al2O3), boehmite, etc., applied to one side of the separator.

[0065] The electrolyte was prepared by dissolving LiPF6 as a supporting salt at a concentration of 1.0 mol / L in a mixed solvent containing ethylene carbonate (EC), dimethyl carbonate (DMC), and ethyl methyl carbonate (EMC) in a volume ratio of 30:30:40.

[0066] A coin cell was fabricated by stacking the negative electrode, separator, and metallic lithium in that order and impregnating them with an electrolyte, with the ceramic layer of the separator facing the negative electrode.

[0067] [Evaluation of discharge specific capacity] Using the evaluation coin cells obtained above, the discharge specific capacity of the recovered negative electrode active materials according to Examples 1 to 15 was evaluated. Specifically, each evaluation coin cell was placed in an environment of 25°C, and charged at a constant current to 3 mV against the lithium counter electrode at a current rate of 0.2 C, and then charged at a constant voltage of 3 mV until the current rate became 1 / 10 C. Then, each evaluation coin cell was discharged at a constant current to 1.6 V against the lithium electrode at a current value of 0.2 C, and then discharged at a constant voltage of 1.6 V until the current rate became 1 / 10 C. In this way, the discharge capacity (mAh) at 0.2 C discharge was obtained. The discharge specific capacity (mAh / g) of the negative electrode active material was calculated from this discharge capacity and the weight (g) of the negative electrode active material. The results are shown in Table 1.

[0068] [Rate performance evaluation] Next, the rate performance was evaluated as an index of the rapid charge / discharge performance of the recovered negative electrode active material according to Example 1 to Example 15 using the above-mentioned evaluation coin cell. Specifically, each evaluation coin cell after the above-mentioned discharge specific capacity measurement was placed in an environment of 25°C, and was charged at a constant current of 3 mV against the lithium counter electrode at a current rate of 1C, and was further charged at a constant voltage of 3 mV until the current rate became 1 / 10C. Then, each evaluation coin cell was discharged at a constant current of 1C against the lithium electrode at a current value of 1.6V, and was further discharged at a constant voltage of 1.6V until the current rate became 1 / 10C. In this way, the discharge capacity (mAh) at 1C discharge was obtained. The rate performance (%) was obtained by the following formula (1) using the discharge capacity (mAh) at 1C discharge and the discharge capacity (mAh) at 0.2C discharge measured during the above-mentioned discharge specific capacity evaluation. It can be said that the higher the value of the rate performance (%), the better the charge / discharge performance of the recovered negative electrode active material. The results are shown in Table 1. Rate performance (%) = (discharge capacity at 1C discharge (mAh) / discharge capacity at 0.2C discharge (mAh)) × 100 Formula (1)

[0069] [Table 1]

[0070] As shown in the results in Table 1, in Example 1, the negative electrode active material was recovered without performing the charging and discharging steps, and the I D / I G and interlayer distance d(002), and good results were obtained for both the discharge specific capacity and rate performance. In addition, from the results of Examples 2 to 4 and Examples 7 to 10, it was found that when the discharge rate was relatively higher than the charge rate, the I D / I G and interlayer distance d(002), and it was found that good results were obtained for both the discharge specific capacity and rate performance. In addition, for Examples 5 and 6, which have different charge end SOCs from Example 1, and Examples 11 to 14, which have different discharge end SOCs, I D / I Gand the interlayer distance d(002), and good results were obtained for both the discharge specific capacity and the rate performance.

[0071] <Study Example 2: Study of the positive and negative electrode capacity ratio in the prepared lithium ion secondary battery> (Example 16 to Example 21) Here, the positive and negative electrode capacity ratios in the lithium ion secondary batteries to be prepared were examined. Specifically, in Examples 16 to 21, lithium ion secondary batteries were prepared with the same configuration as in Example 1 except that the positive and negative electrode capacity ratios were as shown in Table 2. Then, the lithium ion secondary batteries according to Examples 16 to 21 were subjected to a charging process and a discharging process under the same conditions as in Example 1, and the negative electrode active materials according to Examples 16 to 21 were recovered (hereinafter, referred to as "recovered negative electrode active materials"). The recovered negative electrode active materials according to Examples 16 to 21 were evaluated in the same manner as in Study Example 1. The results are shown in Table 2. Thereafter, coin cells for evaluation according to Examples 16 to 21 were produced and evaluated in the same manner as in Study Example 1. The results are shown in Table 2.

[0072] [Table 2]

[0073] As shown in the results in Table 2, in all of Examples 16 to 21 in which the positive and negative electrode capacity ratio was 1.0 or more, better results were obtained in terms of both the discharge specific capacity and the rate performance compared to Example 15 in which the negative electrode active material was recovered without performing the charging and discharging steps.

[0074] As described above, specific aspects of the technology disclosed herein include those described in the following sections. Item 1: A method for regenerating a negative electrode active material from a used lithium ion secondary battery, comprising: A preparation step of preparing a used lithium ion secondary battery including a positive electrode, a negative electrode including a negative electrode active material including a carbon material, and an electrolyte; a charging step of charging the lithium ion secondary battery; a discharging step of discharging the lithium ion secondary battery after the charging step at a discharge rate higher than the charge rate of the charging step; A recovery step of recovering the negative electrode active material including a carbon material from the negative electrode of the lithium ion secondary battery after the discharge step. A method for reproducing negative electrode active material. Item 2: The positive and negative electrode capacity ratio (negative electrode capacity / positive electrode capacity) of the lithium ion secondary battery prepared in the preparation step is 1.0 or more. Item 1. A method for reproducing the negative electrode active material according to item 1. Item 3: The method for reproducing a negative electrode active material according to Item 1 or 2, wherein the charging step is carried out at a charging rate of 0.5 C or less. Item 4: The method for reproducing a negative electrode active material according to any one of Items 1 to 3, wherein the charging step is carried out until the state of charge (SOC) of the lithium ion secondary battery becomes 50% or more. Item 5: The method for reproducing a negative electrode active material according to any one of Items 1 to 4, wherein the discharge step is carried out at a discharge rate of 0.5 C or more. Item 6: The method for reproducing a negative electrode active material according to any one of Items 1 to 5, wherein the discharging step is carried out until the SOC of the lithium ion secondary battery becomes 30% or less. Item 7: The method for reproducing a negative electrode active material according to any one of Items 1 to 6, wherein the ratio (ID / IG) of D band intensity (ID) to G band intensity (IG) of the negative electrode active material recovered in the recovery step, as determined by Raman spectroscopy, is 0.38 or more. Item 8: The method for reproducing a negative electrode active material according to Item 7, wherein the interlayer distance d(002) of the negative electrode active material recovered in the recovery step based on an X-ray diffraction method is 3.350 Å or more and 3.369 Å or less. [Explanation of symbols]

[0075] 1. Lithium-ion secondary battery 10 Cases 12 Positive terminal 14 Negative terminal 16 Liquid injection hole 18 Sealing member 20 Electrode body 30 positive electrode 32 Positive electrode core 34 Cathode active material layer 40 negative electrode 42 Negative electrode core 44 Negative electrode active material layer 46 Negative electrode active material 50 Separator 60 Lithium-ion 62 Solvent molecules

Claims

1. A method for regenerating a negative electrode active material from a used lithium ion secondary battery, comprising the steps of: A preparation step of preparing a used lithium ion secondary battery including a positive electrode, a negative electrode including a negative electrode active material including a carbon material, and an electrolyte; a charging step of charging the lithium ion secondary battery; a discharging step of discharging the lithium ion secondary battery after the charging step at a discharge rate higher than a charge rate of the charging step; A recovery step of recovering the negative electrode active material including a carbon material from the negative electrode of the lithium ion secondary battery after the discharge step. A method for reproducing negative electrode active material.

2. The positive and negative electrode capacity ratio (negative electrode capacity / positive electrode capacity) of the lithium ion secondary battery prepared in the preparation step is 1.0 or more. The method for reproducing the negative electrode active material according to claim 1 .

3. The method for reproducing a negative electrode active material according to claim 1 or 2, wherein the charging step is carried out at a charging rate of 0.5 C or less.

4. 3. The method for reproducing a negative electrode active material according to claim 1, wherein the charging step is performed until the state of charge (SOC) of the lithium ion secondary battery becomes 50% or more.

5. The method for reproducing a negative electrode active material according to claim 1 or 2, wherein the discharging step is carried out at a discharge rate of 0.5 C or more.

6. 3. The method for reproducing a negative electrode active material according to claim 1, wherein the discharging step is performed until the SOC of the lithium ion secondary battery becomes 30% or less.

7. The G band intensity (I Ｇ ) versus D band intensity (I Ｄ ) ratio (I Ｄ / I Ｇ 3. The method for reproducing a negative electrode active material according to claim 1 , wherein the ratio of the positive electrode active material content to the negative electrode active material content is 0.38 or more.

8. 8. The method for reproducing a negative electrode active material according to claim 7, wherein the interlayer distance d(002) of the negative electrode active material recovered in the recovery step based on an X-ray diffraction method is 3.350 Å or more and 3.369 Å or less.

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