Patent Application
20230093960
The present disclosure relates to a positive electrode active material, a positive electrode material, a battery, and a method for manufacturing a positive electrode active material.
Japanese Unexamined Patent Application Publication No. 2018-125214 discloses an all-solid battery including an active material particle and a coating layer that coats at least part of the surface of the active material particle and using a positive electrode active material in which the amount of water that is generated at 200° C. is a predetermined amount or less and a sulfide solid electrolyte. The patent application publication discloses that a lithium ion conductive oxide, such as lithium niobate, lithium titanate, lithium lanthanum zirconate, lithium tantalate, or lithium tungstate, is used as the coating material and that lithium niobate is particularly suitably used.
One non-limiting and exemplary embodiment provides a battery with a high initial charge and discharge efficiency.
In one general aspect, the techniques disclosed here feature a positive electrode active material of including a complex oxide represented by a formula (1): LiNixMe1-xO2 as a main component and containing water generated during heating at 300° C. in Karl Fischer titration in an amount of 317.5 ppm by mass or less. Here, x satisfies 0.5 ≤ x ≤ 1, and Me is at least one element selected from the group consisting of Mn, Co, and Al.
According to the present disclosure, a battery with a high initial charge and discharge efficiency can be obtained.
It should be noted that general or specific embodiments may be implemented as a system, a method, an integrated circuit, a computer program, a storage medium, or any selective combination thereof.
Additional benefits and advantages of the disclosed embodiments will become apparent from the specification and drawings. The benefits and/or advantages may be individually obtained by the various embodiments and features of the specification and drawings, which need not all be provided in order to obtain one or more of such benefits and/or advantages.
The present inventors diligently studied factors that vary the initial efficiency of a battery. As a result, the present inventors have found that trace amounts of water, hydrated water, hydroxyl groups, etc. contained in an active material cause side reactions with a solid electrolyte to decrease the initial efficiency. The present inventors considered based on this finding that when an active material is manufactured, treatment for significantly reducing the amount of water in the active material and hydrated water, hydroxyl groups, and so on originated from the water is necessary and proceeded with further research. As a result, it was possible to find that when an active material is manufactured, water, hydrated water, hydroxyl groups, etc. contained in the active material can be greatly reduced by performing drying under specified conditions. In addition, it was found that water, hydrated water, and hydroxyl groups contained in an active material can be quantitatively measured with the amount of water generated when the active material is heated to 300° C. In detail, the amount of water generated by heating an active material to 200° C. generally corresponds to the water including hydrated water present on the active material surface, and the amount of water generated by heating to 200° C. to 300° C. corresponds to the water generated by decomposition of hydroxyl groups on the active material surface or impurities derived therefrom. A battery having a high initial charge and discharge efficiency could be obtained by manufacturing the battery using the thus-manufactured active material. Outline of an aspect according to the present disclosure
A positive electrode active material according to a 1st aspect of the present disclosure includes a complex oxide represented by a formula (1): LiNixMe1-x02 as a main component and contains water generated during heating at 300° C. in Karl Fischer titration in an amount of 317.5 ppm by mass or less. Here, x satisfies 0.5 ≤ x ≤ 1; and Me is at least one element selected from the group consisting of Mn, Co, and Al.
In the positive electrode active material according to the 1st aspect, a high initial charge and discharge efficiency of a battery can be realized.
In a 2nd aspect of the present disclosure, for example, the positive electrode active material according to the 1st aspect further includes a coating material coating the surface of the positive electrode active material, and the coating material may include lithium element (Li) and at least one element selected from the group consisting of oxygen element (O), fluorine element (F), and chlorine element (Cl).
In the positive electrode active material according to the 2nd aspect, a high initial charge and discharge efficiency of a battery can be realized.
In a 3rd aspect of the present disclosure, for example, in the positive electrode active material according to the 2nd aspect, the coating material may include at least one selected from the group consisting of lithium niobate, lithium phosphate, lithium titanate, lithium tungstate, lithium fluorozirconate, lithium fluoroaluminate, lithium fluorotitanate, and lithium fluoromagnesate.
In the positive electrode active material according to the 3rd aspect, a high initial charge and discharge efficiency of a battery can be realized.
The positive electrode material according to a 4th aspect of the present disclosure includes the positive electrode active material according to any one of the 1st to 3rd aspects and a solid electrolyte.
In the positive electrode material according to the 4th aspect, a high initial charge and discharge efficiency of a battery can be realized.
In a 5th aspect of the present disclosure, for example, in the positive electrode material according to the 4th aspect, the solid electrolyte is represented by a formula (2): LiαMβXγ. Here, α, β, and γ are each independently a value larger than 0; M includes at least one selected from the group consisting of metallic elements excluding Li and metalloid elements; and X includes at least one selected from the group consisting of F, Cl, Br, and I.
In the positive electrode material according to the 5th aspect, a high initial charge and discharge efficiency of a battery can be realized.
In a 6th aspect of the present disclosure, for example, in the positive electrode material according to the 5th aspect, M may include yttrium.
In the positive electrode material according to the 6th aspect, a high initial charge and discharge efficiency of a battery can be realized.
In a 7th aspect of the present disclosure, for example, in the positive electrode material according to the 5th or 6th aspect, the formula (2) may satisfy 2.5 ≤ α ≤ 3, 1 ≤ β ≤ 1.1, and γ = 6.
In the positive electrode material according to the 7th aspect, a high initial charge and discharge efficiency of a battery can be realized.
In an 8th aspect of the present disclosure, for example, in the positive electrode material according to any one of the 5th to 7th aspects, X may include at least one selected from the group consisting of Cl and Br.
In the positive electrode material according to the 8th aspect, a high initial charge and discharge efficiency of a battery can be realized.
A battery according to a 9th aspect of the present disclosure includes a positive electrode containing the positive electrode material according to any one of the 4th to 8th aspects, a negative electrode, and an electrolyte layer disposed between the positive electrode and the negative electrode.
In the battery according to the 9th aspect, a high initial charge and discharge efficiency of a battery can be realized.
In a 10th aspect of the present disclosure, for example, in the battery according to the 9th aspect, the electrolyte layer may contain the solid electrolyte.
In the battery according to the 10th aspect, a high initial charge and discharge efficiency of a battery can be realized.
In an 11th aspect of the present disclosure, for example, in the battery according to the 9th or 10th aspect, the electrolyte layer may contain a halide solid electrolyte different from the solid electrolyte.
In the battery according to the 11th aspect, a high initial charge and discharge efficiency of a battery can be realized.
In a 12th aspect of the present disclosure, for example, in the battery according to any one of the 9th to 11th aspects, the electrolyte layer may contain a sulfide solid electrolyte.
In the battery according to the 12th aspect, a high initial charge and discharge efficiency of a battery can be realized.
A method for manufacturing a positive electrode active material according to a 13th aspect of the present disclosure is a method for manufacturing the positive electrode active material according to any one of the 1st to 3rd aspects, wherein
According to the manufacturing method according to the 13th aspect, a positive electrode active material containing a low amount of water that is generated during heating at 300° C. in Karl Fischer titration can be manufactured. Consequently, a high initial charge and discharge efficiency of a battery can be realized.
Embodiments of the present disclosure will now be described with reference to the drawings.
The positive electrode material 1000 in the embodiment includes a solid electrolyte 100 and a positive electrode active material 110. As shown in
Here, the positive electrode active material 110 includes a complex oxide represented by a formula (1): LiNixMe1-xO2 as a main component and contains water generated during heating at 300° C. in Karl Fischer titration in an amount of 317.5 ppm by mass or less, wherein X satisfies 0.5 ≤ x ≤ 1, and Me is at least one element selected from Mn, Co, and Al.
According to the above configuration, a high initial charge and discharge efficiency of a battery can be improved.
Here, the term “main component” refers to the most abundant component by mass ratio.
The amount of water in the positive electrode active material 110 is specified by measuring the amount of water generated during heating at 300° C. in Karl Fischer titration. The water generated at 300° C. is inferred to be mainly water physically adsorbed to the positive electrode active material 110 and hydrated water and hydroxyl groups binding to, for example, surface impurities.
The positive electrode active material 110 may contain a material that can be used as the active material of an all-solid lithium ion battery in addition to the complex oxide represented by the formula (1).
Examples of the material that can be used as the active material of an all-solid lithium ion battery include LiCoO2, LiNixCo1-xO2 (0 < x < 0.5), LiNi⅓Co⅓Mn⅓O2, LiMnO2, a different kind element substituent Li—Mn spinel (e.g., LiMn1.5Ni0.5O4, LiMn1.5Al0.5O4, LiMn1.5Mg0.5O4, LiMn1.5Co0.5O4, LiMn1.5Fe0.5O4, or LiMn1.5Zn0.5O4), lithium titanate (e.g., Li4Ti5O12), lithium metal phosphate (e.g., LiFePO4, LiMnPO4, LiCoPO4, and LiNiPO4), and a transition metal oxide (e.g., V2O5 and MoO3).
Among the above-mentioned materials, a lithium-containing complex oxide selected from, for example, LiCoO2, LiNixCo1-xO2 (0 < x < 0.5), LiNi⅓Co⅓Mn⅓O2, LiMnO2, a different kind element substituent Li—Mn spinel, and lithium metal phosphate is preferable.
In the positive electrode active material 110, the amount of water generated during heating at 300° C. in Karl Fischer titration is 317.5 ppm by mass or less. In application to an all-solid lithium ion battery, the solid electrolyte 100 described later can be prevented from being deteriorated due to water contained in the positive electrode active material 110 by suppressing the amount of water in the positive electrode active material 110 to 317.5 ppm by mass or less to maintain a high conductivity of the solid electrolyte 100. Accordingly, a battery with a low battery resistance is provided by using the positive electrode active material 110.
The positive electrode active material 110 is dried by heating at a temperature of 70° C. or more and 850° C. or less for 1 hour or more prior to constituting a positive electrode material. On this occasion, the atmosphere during drying may be vacuum or normal pressure and may be an atmosphere of a dew point of -60° C. or less. As long as the dew point is -60° C. or less, the drying may be performed in a nitrogen gas or in an oxygen gas. The dried positive electrode active material is subjected to measurement of the amount of water generated during heating at 300° C. with a Karl Fischer moisture analyzer.
For a complex oxide having a composition satisfying 0.5 ≤ x ≤ 1 in the formula (1), deterioration of the surface due to a reaction between the physically adsorbed water and the active material during high-temperature drying is of concern. Accordingly, it is desirable to sufficiently remove physically adsorbed water from the complex oxide at low temperature.
The positive electrode active material 110 may be dried by heating at a temperature of 70° C. or more and less than 150° C. for 12 hours or more or by heating at a temperature of 150° C. or more and 850° C. or less for 0.5 hours or more in advance prior to constituting a positive electrode material.
Heating within a range of 70° C. or more and less than 150° C. may be performed for 500 hours or less. That is, heating within a range of 70° C. or more and less than 150° C. may be performed for 12 hours or more and 500 hours or less. Heating within a range of 70° C. or more and less than 150° C. may be performed for 24 hours or more and 350 hours or less.
Heating within a range of 150° C. or more and 850° C. or less may be performed for 24 hours or less. That is, heating within a range of 150° C. or more and 850° C. or less may be performed for 0.5 hours or more and 24 hours or less. Heating within a range of 150° C. or more and 850° C. or less may be performed for 1 hour or more and 12 hours or less.
In the positive electrode active material 110, the amount of water generated during heating at 300° C. in Karl Fischer titration may be 8.8 ppm by mass or more. That is, the amount of water generated during heating at 300° C. in Karl Fischer titration may be 8.8 ppm by mass or more and 317.5 ppm by mass or less.
The positive electrode active material 110 may include a coating material 120 on the surface thereof. Incidentally, the coating material 120 may coat the entire surface of the positive electrode active material 110 or may partially coat the surface.
The coating material 120 may contain Li and at least one element selected from the group consisting of O, F, and Cl.
The coating material 120 may contain at least one selected from the group consisting of lithium niobate, lithium phosphate, lithium titanate, lithium tungstate, lithium fluorozirconate, lithium fluoroaluminate, lithium fluorotitanate, and lithium fluoromagnesate.
As the solid electrolyte material included in the solid electrolyte 100, a halide solid electrolyte may be used.
The solid electrolyte 100 may be a compound represented by a formula (2): LiaMβXy. Here, α, β, and y are values larger than 0; M includes at least one selected from the group consisting of metallic elements excluding Li and metalloid elements; and X includes at least one element selected from the group consisting of F, Cl, Br, and I.
Here, the metalloid element is B, Si, Ge, As, Sb, or Te. The metallic element is any of all elements in Groups 1 to 12 of the Periodic Table excluding hydrogen or any of all elements in Groups 13 to 16 excluding the above-mentioned metalloid elements, C, N, P, O, S, and Se. That is, the metallic elements are those in a group of elements that can become cations when form a halogen compound or an inorganic compound.
As the solid electrolyte 100, for example, Li3YX6, Li2MgX4, Li2FeX4, Li(Al,Ga,In)X4, or Li3(Al,Ga,In)X6 can be used. Here, X is at least one selected from the group consisting of F, Cl, Br, and I.
In the present disclosure, “(A,B,C)” means “at least one selected from the group consisting of A, B, and C”.
According to the above configuration, the resistance of a battery can be reduced. Accordingly, the charge and discharge characteristics of a battery are improved.
The formula (2) may satisfy 2.5 ≤ α ≤ 3, 1 ≤ β ≤ 1.1, and y = 6.
In the formula (2), X may include at least one selected from the group consisting of Cl and Br.
In the formula (2), M may include yttrium (Y).
The solid electrolyte including Y may be, for example, a compound represented by a composition formula of LiaM'bYcX6. Here, a + mb + 3c = 6 and c > 0 are satisfied; M′ is at least one selected from the group consisting of metallic elements excluding Li and Y and metalloid elements; m denotes the valence of M′; and X is at least one selected from the group consisting of F, Cl, Br, and I.
As the M′, at least one selected from the group consisting of Mg, Ca, Sr, Ba, Zn, Sc, Al, Ga, Bi, Zr, Hf, Ti, Sn, Ta, and Nb may be used.
As the solid electrolyte including Y, specifically, Li3YF6, Li3YCl6, Li3YBr6, Li3YI6, Li3YBrCl5, Li3YBr3Cl3, Li3YBr5Cl, Li3YBr5I, Li3YBr3I3, Li3YBrI5, Li3YClI5, Li3YCl3I3, Li3YCl5I, Li3YBr2Cl2I2, Li3YBrCl4I, Li2.7Y1.1Cl6, Li2.5Y0.5Zr0.5Cl6, Li2.5Y0.3Zr0.7Cl6, etc. can be used.
According to the above configuration, the resistance of a battery can be further reduced.
Incidentally, the halide solid electrolyte does not have to include sulfur. In addition, the shapes of the solid electrolyte 100 and the positive electrode active material 110 in Embodiment 1 are not particularly limited and may be, for example, needle, spherical, or oval spherical. For example, the shapes of the solid electrolyte 100 and positive electrode active material 110 may be particulate.
For example, when the shape of the solid electrolyte 100 in Embodiment 1 is particulate (e.g., spherical), the median diameter may be 100 µm or less.
When the median diameter of the solid electrolyte 100 is 100 µm or less, the positive electrode active material 110 and the solid electrolyte 100 can form a good dispersion state in the positive electrode material 1000. Consequently, the charge and discharge characteristics of a battery are improved.
In addition, in Embodiment 1, the median diameter of the solid electrolyte 100 may be 10 µm or less.
According to the above configuration, in the positive electrode material 1000, the positive electrode active material 110 and the solid electrolyte 100 can form a good dispersion state.
In addition, in Embodiment 1, the median diameter of the solid electrolyte 100 may be smaller than that of the positive electrode active material 110.
According to the above configuration, the solid electrolyte 100 and the positive electrode active material 110 can form a better dispersion state in the positive electrode material 1000.
The median diameter of the positive electrode active material 110 may be 0.1 µm or more and 100 µm or less.
When the median diameter of the positive electrode active material 110 is 0.1 µm or more, in the positive electrode material 1000, the positive electrode active material 110 and the solid electrolyte 100 can form a good dispersion state. As this result, the charge and discharge characteristics of a battery are improved.
When the median diameter of the positive electrode active material 110 is 100 µm or less, the diffusion speed of lithium in the positive electrode active material 110 can be sufficiently secured. Consequently, high-output operation of the battery is possible.
In the present disclosure, the “median diameter” means the particle diameter at which the accumulated volume is equal to 50% in a volume-based particle size distribution. The volume-based particle size distribution is measured with, for example, a laser diffraction measurement apparatus or an image analyzer.
Incidentally, in the positive electrode material 1000 in Embodiment 1, particles of the solid electrolyte 100 and particles of the positive electrode active material 110 may be in contact with each other as shown in
The positive electrode material 1000 in Embodiment 1 may include particles of a plurality of solid electrolytes 100 and particles of a plurality of positive electrode active materials 110.
In addition, in the positive electrode material 1000 in Embodiment 1, the content of the solid electrolyte 100 and the content of the positive electrode active material 110 may be the same as or different from each other.
Embodiment 2 will now be described. The description overlapping with that of Embodiment 1 will be appropriately omitted.
The battery 2000 in Embodiment 2 includes a positive electrode 201, an electrolyte layer 202, and a negative electrode 203.
The positive electrode 201 includes the positive electrode material 1000.
The electrolyte layer 202 is disposed between the positive electrode 201 and the negative electrode 203.
According to the above configuration, the discharge voltage of a battery can be improved.
The volume ratio of the positive electrode active material 110 and the solid electrolyte 100 contained in the positive electrode 201, “v1 : 100 - v1”, may satisfy 30 ≤ v1 ≤ 95. When 30 ≤ v1 is satisfied, an energy density of the battery 2000 is sufficiently secured. When v1 ≤ 95 is satisfied, high-output operation is possible.
The thickness of the positive electrode 201 may be 10 µm or more and 500 µm or less. When the thickness of the positive electrode 201 is 10 µm or more, an energy density of the battery 2000 is sufficiently secured. When the thickness of the positive electrode 201 is 500 µm or less, high-output operation is possible.
The electrolyte layer 202 is a layer containing an electrolyte material. The electrolyte material is, for example, a solid electrolyte material. That is, the electrolyte layer 202 may be a solid electrolyte layer. As the solid electrolyte, the materials exemplified as the material of the solid electrolyte 100 in Embodiment 1 may be used. That is, the electrolyte layer 202 may contain a solid electrolyte having the same composition as that of the solid electrolyte 100 contained in the positive electrode material 1000.
According to the above configuration, the charge and discharge efficiency of the battery 2000 can be further improved.
The electrolyte layer 202 may contain a halide solid electrolyte having a composition different from that of the solid electrolyte contained in the positive electrode material 1000.
The electrolyte layer 202 may contain a sulfide solid electrolyte.
The electrolyte layer 202 may contain only one solid electrolyte selected from the group of the above-mentioned solid electrolytes or may contain two or more solid electrolytes selected from the group of the above-mentioned solid electrolytes. Plurality of solid electrolytes have compositions different from each other. For example, the electrolyte layer 202 may contain a halide solid electrolyte and a sulfide solid electrolyte.
The thickness of the electrolyte layer 202 may be 1 µm or more and 300 µm or less. When the thickness of the electrolyte layer 202 is 1 µm or more, the positive electrode 201 and the negative electrode 203 are unlikely to be short-circuited. When the thickness of the electrolyte layer 202 is 300 µm or less, high-output operation is possible.
The negative electrode 203 contains a material that has a property of occluding and releasing metal ions (e.g., lithium ions). The negative electrode 203 contains, for example, a negative electrode active material.
As the negative electrode active material, for example, a metal material, a carbon material, an oxide, a nitride, a tin compound, or a silicon compound can be used. The metal material may be a single metal. Alternatively, the metal material may be an alloy. Examples of the metal material include lithium metals and lithium alloys. Examples of the carbon material include natural graphite, coke, carbon under graphitization, carbon fibers, spherical carbon, artificial graphite, and amorphous carbon. From the viewpoint of capacity density, silicon (Si), tin (Sn), a silicon compound, or a tin compound can be suitably used.
The negative electrode 203 may contain a solid electrolyte material. According to the above configuration, the lithium ion conductivity in the negative electrode 203 can be enhanced, and high-output operation is possible. As the solid electrolyte, the materials exemplified in Embodiment 1 may be used. That is, the negative electrode 203 may contain a solid electrolyte having the same composition as that of the solid electrolyte contained in the positive electrode material 1000.
The median diameter of the negative electrode active material may be 0.1 µm or more and 100 µm or less.
When the median diameter of the negative electrode active material is 0.1 µm or more, the negative electrode active material and the solid electrolyte material can form a good dispersion state. As a result, the charge and discharge characteristics of a battery are improved.
In addition, when the median diameter of the negative electrode active material is 100 µm or less, the diffusion speed of lithium in the negative electrode active material can be sufficiently secured. Consequently, high-output operation of the battery is possible.
The median diameter of the negative electrode active material may be larger than that of the solid electrolyte material. Consequently, the negative electrode active material and the solid electrolyte material can form a good dispersion state.
The volume ratio of the negative electrode active material and the solid electrolyte material contained in the negative electrode 203, “v2 : 100 - v2”, may satisfy 30 ≤ v2 ≤ 95. When 30 ≤ v2 is satisfied, an energy density of the battery 2000 is sufficiently secured. When v2 ≤ 95 is satisfied, high-output operation is possible.
The thickness of the negative electrode 203 may be 10 µm or more and 500 µm or less. When the thickness of the negative electrode 203 is 10 µm or more, an energy density of the battery 2000 is sufficiently secured. When the thickness of the negative electrode 203 is 500 µm or less, high-output operation is possible.
At least one selected from the group consisting of the positive electrode 201, the electrolyte layer 202, and the negative electrode 203 may include a binder for the purpose of improving the adhesion between particles. The binder is used for improving the adhesion of the materials constituting the electrode. Examples of the binder include polyvinylidene fluoride, polytetrafluoroethylene, polyethylene, polypropylene, aramid resin, polyamide, polyimide, polyamideimide, polyacrylonitrile, polyacrylic acid, polyacrylic acid methyl ester, polyacrylic acid ethyl ester, polyacrylic acid hexyl ester, polymethacrylic acid, polymethacrylic acid methyl ester, polymethacrylic acid ethyl ester, polymethacrylic acid hexyl ester, polyvinyl acetate, polyvinyl pyrrolidone, polyether, polyether sulfone, hexafluoropolypropylene, styrene-butadiene-rubber, and carboxymethylcellulose. In addition, as the binder, a copolymer of two or more materials selected from tetrafluoroethylene, hexafluoroethylene, hexafluoropropylene, perfluoroalkylvinylether, vinylidene fluoride, chlorotrifluoroethylene, ethylene, propylene, pentafluoropropylene, fluoromethylvinylether, acrylic acid, and hexadiene can be used. Moreover, a mixture of two or more selected from these materials may be used as the binder.
At least one selected from the group consisting of the positive electrode 201 and the negative electrode 203 may include a conductive assistant for the purpose of enhancing the electron conductivity. As the conductive assistant, for example, graphite such as natural graphite or artificial graphite, carbon black such as acetylene black or Ketjen black, a conductive fiber such as a carbon fiber or a metal fiber, a metal powder such as fluorinated carbon or aluminum, a conductive whisker such as zinc oxide or potassium titanate, a conductive metal oxide such as titanium oxide, or a conductive polymer compound such as polyaniline, polypyrrole, or polythiophene can be used. In the case of using a carbon conductive assistant, it is possible to reduce the cost.
Incidentally, the battery in Embodiment 2 can be configured as batteries of various shapes, such as a coin type, a cylindrical type, a square type, a sheet type, a button type, a flat type, and a stacked type.
The present disclosure will now be described in more detail with reference to Examples.
A positive electrode active material, LiNi0.8(Co,Mn)0.2O2, was vacuum-dried at 100° C. for 2 weeks and was then taken out in a dry atmosphere with a dew point of -20° C. or less. Hereinafter, LiNi0.8(Co,Mn)0.2O2 is referred to as NCM. Thus, a positive electrode active material of Example 1 was obtained.
In the present Example, it was confirmed that a positive electrode active material with sufficiently removed physically adsorbed water is obtained by vacuum drying at 100° C. for 2 weeks. Specifically, it was confirmed that in the positive electrode active material according to the present Example, the amount of water measured by Karl Fischer titration at about 120° C. is 1 ppm or less.
The amount of water generated at 300° C. in the positive electrode active material produced in Example 1 was measured with a Karl Fischer moisture analyzer (manufactured by Nittoseiko Analytech Co., Ltd., CA-310). The heating temperature of the measurement sample was set to 300° C. The amount of water generated in the positive electrode active material of Example 1 was 317.5 ppm by mass.
Raw material powders, LiCl, LiBr, and YCl3, were weighed at a molar ratio, LiCl : LiBr : YCl3, of 1 : 2 : 1 in an argon glove box with a dew point of -60° C. or less. These powders were pulverized and mixed in a mortar. Subsequently, milling treatment was performed using a planetary ball mill at 600 rpm for 12 hours.
As in above, a powder of halide solid electrolyte represented by a composition formula Li3YBr2Cl4 was obtained.
A halide solid electrolyte and the positive electrode active material of Example 1 were weighed at a mass ratio of 20 : 80 in an argon glove box with a dew point of -60° C. or less. These materials were mixed in an agate mortar to produce a positive electrode material of Example 1.
Li2S and P2S5 were weighed at a molar ratio, Li2S : P2S5, of 75 : 25 in an argon glove box with a dew point of -60° C. or less. These materials were pulverized and mixed in a mortar. Subsequently, milling treatment was performed using a planetary ball mill (manufactured by Fritsch, P-7 type) at 510 rpm for 10 hours to obtain a glass-like solid electrolyte. The glass-like solid electrolyte was heat-treated in an inert atmosphere at 270° C. for 2 hours. Consequently, a glass-ceramic-like sulfide solid electrolyte was obtained.
The following process was performed using the above-described halide solid electrolyte, positive electrode material of Example 1, and sulfide solid electrolyte.
First, the sulfide solid electrolyte (80 mg), the halide solid electrolyte (40 mg), and the positive electrode material (12 mg) of Example 1 were stacked in this order in an insulating outer cylinder and were pressure-molded at a pressure of 720 MPa to obtain a positive electrode and a solid electrolyte layer.
Subsequently, metallic Li (thickness: 200 µm) was stacked on the solid electrolyte layer on the opposite side to the side in contact with the positive electrode, followed by pressure-molding at a pressure of 80 MPa to produce a stack composed of the positive electrode, the solid electrolyte layer, and a negative electrode.
Subsequently, current collectors made of stainless steel were disposed on opposite sides of the stack, and the current collectors were provided with current collector leads.
Ultimately, the inside of the insulating outer cylinder was isolated from the outside atmosphere by sealing the insulating outer cylinder using an insulating ferrule to produce a battery of Example 1.
A charge and discharge test was performed using the battery of Example 1 under the following conditions.
The battery was disposed in a thermostatic tank of 25° C. and connected to a potentiostat (manufactured by Solartron Analytical) loaded with a frequency response analyzer.
Constant current charging was performed at a current value of 96 µA corresponding to 0.05 C rate (20-hour rate) with respect to the theoretical capacity of the battery, and the charging was ended at a voltage of 4.3 V. Subsequently, similarly, constant current discharging was performed at a current value of 96 µA corresponding to 0.05 C rate (20-hour rate), and the discharging was ended at a voltage of 2.5 V.
The charging capacity of the battery of Example 1 was 2006.7 µAh, the discharging capacity was 1819.6 µAh, and the initial charge and discharge efficiency was 90.7%.
NCM was vacuum-dried at 100° C. for 2 weeks and was then heat-treated at 300° C. for 1 hour in a nitrogen gas atmosphere. Subsequently, the NCM was taken out in a dry atmosphere with a dew point of -20° C. or less. Thus, a positive electrode active material of Example 2 was obtained.
NCM was vacuum-dried at 100° C. for 2 weeks and was then heat-treated at 400° C. for 1 hour in a nitrogen gas atmosphere. Subsequently, the NCM was taken out in a dry atmosphere with a dew point of -20° C. or less. Thus, a positive electrode active material of Example 3 was obtained.
NCM was vacuum-dried at 100° C. for 2 weeks and was then heat-treated at 500° C. for 1 hour in a nitrogen gas atmosphere. Subsequently, the NCM was taken out in a dry atmosphere with a dew point of -20° C. or less. Thus, a positive electrode active material of Example 4 was obtained.
NCM was vacuum-dried at 100° C. for 2 weeks and was then heat-treated at 600° C. for 1 hour in a nitrogen gas atmosphere. Subsequently, the NCM was taken out in a dry atmosphere with a dew point of -20° C. or less. Thus, a positive electrode active material of Example 5 was obtained.
NCM was vacuum-dried at 100° C. for 2 weeks and was then heat-treated at 800° C. for 1 hour in a nitrogen gas atmosphere. Subsequently, the NCM was taken out in a dry atmosphere with a dew point of -20° C. or less. Thus, a positive electrode active material of Example 6 was obtained.
The amounts of water generated at 300° C. in the positive electrode active materials produced in Examples 2 to 6 were measured as in Example 1. The amounts of water generated in the positive electrode active materials of Examples 2 to 6 are shown in Table 1 below.
Positive electrode materials of Examples 2 to 6 were produced as in Example 1 except that the positive electrode active materials of Examples 2 to 6 were respectively used as the positive electrode active materials.
Batteries of Examples 2 to 6 were produced as in Example 1 except that the positive electrode materials of Examples 2 to 6 were respectively used as the positive electrode materials.
A charge and discharge test was performed as in Example 1 using the batteries of Examples 2 to 6. The initial charge and discharge efficiencies of the batteries of Examples 2 to 6 are shown in Table 1 below.
NCM that has not been subjected to vacuum drying and heat treatment was used as the positive electrode active material of Comparative Example 1.
The amount of water generated at 300° C. in the positive electrode active material of Comparative Example 1 was measured as in Example 1. The amount of water generated in the positive electrode active material of Comparative Example 1 is shown Table 1 below.
A positive electrode material of Comparative Example 1 was produced as in Example 1 except that the positive electrode active material of Comparative Example 1 was used as the positive electrode active material.
A battery of Comparative Example 1 was produced as in Example 1 using Li3YBr2Cl4, the positive electrode material of Comparative Example 1, and the sulfide solid electrolyte.
A charge and discharge test was performed as in Example 1 using the battery of Comparative Example 1. The initial charge and discharge efficiency of the battery of Comparative Example 1 is shown in Table 1 below.
It is demonstrated from the results shown in Table 1 that it is not easy to remove water-driven impurities from an active material even by drying treatment at 300° C. or more. This is related to the fact that the surface activity of the active material is increased by removing water-driven impurities and thereby water-driven impurities are generated again due to the dew-point environment.
The initial charge and discharge efficiency of a battery is improved by using a positive electrode active material in which the amount of water generated is reduced to 317.5 ppm by mass or less. Further desirably, the amount of water generated may be 52.6 ppm by mass or less. In addition, the amount of water generated at 300° C. may be 8.8 ppm by mass or more. That is, the amount of water generated may be 8.8 ppm by mass or more and 317.5 ppm by mass or less or 8.8 ppm by mass or more and 52.6 ppm by mass or less. The amount of water generated may be 8.8 ppm by mass or more and 35.2 ppm by mass or less.
The battery of the present disclosure can be used, for example, as an all-solid battery.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2020-092708 | May 2020 | JP | national |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/JP2021/019286 | May 2021 | WO |
| Child | 18051873 | US |
