Positive electrode, battery, and method for manufacturing a positive electrode

Abstract

A positive electrode 1000 comprises a mixture of a positive electrode active material 110, a solid electrolyte 100, and a conductive material 140. The conductive material 140 contains carbon black 150 having an average particle diameter of 100nm or less. When a cross-section of the positive electrode 1000 is observed using a scanning electron microscope, a region is observed between the positive electrode active material 110 and the solid electrolyte 100, the region having a concentration of carbon black 150 present therein.

Description

[Technical Field]

[0001] This disclosure relates to a positive electrode, a battery, and a method for manufacturing a positive electrode. [Background technology]

[0002] Patent Document 1 discloses a battery comprising a positive electrode containing a positive electrode active material and a solid electrolyte. [Prior art documents] [Patent Documents]

[0003] [Patent Document 1] Japanese Patent Publication No. 2015-076180 [Overview of the project]

[0004] In conventional technology, it is desirable to further reduce the resistance of the battery.

[0005] In one aspect of this disclosure, the positive electrode is: A positive electrode comprising a mixture of a positive electrode active material, a solid electrolyte, and a conductive material, The conductive material contains carbon black having an average particle size of 100 nm or less. When the cross-section of the positive electrode is observed using a scanning electron microscope, a region in which the carbon black is concentrated between the positive electrode active material and the solid electrolyte is observed.

[0006] According to this disclosure, the resistance of the battery can be reduced. [Brief explanation of the drawing]

[0007] [Figure 1] Figure 1 is a cross-sectional view showing the schematic configuration of the positive electrode in Embodiment 1. [Figure 2] Figure 2 is a flowchart showing the method for manufacturing the positive electrode in Embodiment 1. [Figure 3] Figure 3 is a cross-sectional view showing the schematic configuration of the positive electrode in Modification 1. [Figure 4] Figure 4 is a flowchart showing the method for manufacturing the positive electrode in Modification Example 1. [Figure 5] Figure 5 is a cross-sectional view showing the schematic configuration of the positive electrode in Modification Example 2. [Figure 6] Figure 6 is a cross-sectional view showing the schematic configuration of the positive electrode in modified example 3. [Figure 7] Figure 7 is a cross-sectional view showing the schematic configuration of the battery in Embodiment 2. [Figure 8] Figure 8 shows a cross-sectional SEM image of the positive electrode of Example 1. [Modes for carrying out the invention]

[0008] (Knowledge that forms the basis of this disclosure) Patent Document 1 discloses a battery having a positive electrode comprising a positive electrode active material and a solid electrolyte. Patent Document 1 also states that the positive electrode may contain a conductive additive such as carbon black.

[0009] The inventors diligently researched methods to reduce the resistance of all-solid-state lithium-ion batteries. As a result, they found that the battery's resistance decreases as the amount of carbon black particles placed on the surface of the positive electrode active material increases. This is presumed to be because the carbon black increases the number of electron conduction paths formed on the surface of the positive electrode active material, thereby increasing the effective reaction area of ​​the positive electrode active material. Based on this finding, the inventors further discovered an optimal carbon black coverage ratio of the positive electrode active material surface that minimizes the inhibition of lithium ion conduction between the positive electrode active material and the solid electrolyte.

[0010] (Summary of one aspect of this disclosure) The positive electrode relating to the first aspect of this disclosure is A positive electrode comprising a mixture of a positive electrode active material, a solid electrolyte, and a conductive material, The conductive material contains carbon black having an average particle size of 100 nm or less. When observing the cross-section of the positive electrode using a scanning electron microscope, a region where the carbon black is concentrated and present between the positive electrode active material and the solid electrolyte is observed.

[0011] According to the above configuration, due to the region where the carbon black present between the positive electrode active material and the solid electrolyte is concentrated and present, the effective reaction area of the positive electrode active material increases. Thereby, the resistance of the battery can be reduced.

[0012] In the second aspect of the present disclosure, for example, in the positive electrode according to the first aspect, x obtained by the following formula (1) may satisfy 0% < x < 100%. x = (3·c) / (4·a·b)×10 5 ···(1) In the formula (1), a is the BET (Brunauer-Emmett-Teller) specific surface area (m 2 / g) of the positive electrode active material, b is the average particle diameter (nm) of the carbon black, c is the ratio of the mass of the carbon black to the mass of the positive electrode active material contained in the positive electrode, and the density of the carbon black is 2.0 (g / cm 3 ). According to the above configuration, the resistance of the battery can be reduced.

[0013] In the third aspect of the present disclosure, for example, in the positive electrode according to the second aspect, in the formula (1), x may satisfy 5% ≤ x ≤ 60%. According to the above configuration, the resistance of the battery can be further reduced.

[0014] In the fourth aspect of the present disclosure, for example, in the positive electrode according to the second aspect, in the formula (1), x may satisfy 10% ≤ x ≤ 50%. According to the above configuration, the resistance of the battery can be further reduced.

[0015] In the fifth aspect of the present disclosure, for example, in the positive electrode according to the second aspect, in the formula (1), x1 may satisfy 15% ≤ x1 ≤ 40%. According to the above configuration, the resistance of the battery can be further reduced.

[0016] In the sixth aspect of the present disclosure, for example, in the positive electrode according to any one of the second to fifth aspects, in the formula (1), a may satisfy 0 < a ≤ 1.5. According to the above configuration, it is easy to effectively arrange carbon black on the surface of the positive electrode active material.

[0017] In the seventh aspect of the present disclosure, for example, in the positive electrode according to any one of the first to sixth aspects, the conductive material may further include a fibrous carbon material. According to the above configuration, the electron conductivity in the positive electrode can be further improved.

[0018] In the eighth aspect of the present disclosure, for example, in the positive electrode according to any one of the first to seventh aspects, the ratio of the mass of the conductive material to the mass of the positive electrode active material may be 0.03 or less. According to the above configuration, it is difficult for the conductive material to inhibit the lithium ion conduction between the positive electrode active material and the solid electrolyte.

[0019] In the ninth aspect of the present disclosure, for example, in the positive electrode according to any one of the first to eighth aspects, the carbon black may have an average particle size of 25 nm or less. According to the above configuration, it becomes easier for carbon black to adhere to the surface of the positive electrode active material.

[0020] In the tenth aspect of the present disclosure, for example, in the positive electrode according to any one of the first to ninth aspects, the carbon black may include acetylene black. According to the above configuration, the electron conductivity in the positive electrode can be further improved.

[0021] In the eleventh aspect of the present disclosure, for example, in the positive electrode according to any one of the first to tenth aspects, the solid electrolyte may include at least one selected from the group consisting of a sulfide solid electrolyte and a halide solid electrolyte. According to the above configuration, the output characteristics of the battery can be improved.

[0022] In a twelfth aspect of this disclosure, for example, in a positive electrode according to any one of the first to eleventh aspects, the positive electrode active material may have a layered rock salt structure. In a layered rock salt structure, the transition metal and lithium are regularly arranged to form a two-dimensional plane, thus enabling two-dimensional diffusion of lithium. Therefore, with the above configuration, the energy density of the battery can be improved.

[0023] In a thirteenth aspect of this disclosure, for example, the positive electrode according to any one of the first to twelfth aspects may further include a coating layer that covers at least a portion of the surface of the positive electrode active material. With this configuration, the resistance of the battery can be further reduced.

[0024] The battery relating to the 14th aspect of this disclosure is A positive electrode relating to any one of the first to thirteenth embodiments, The negative electrode and, An electrolyte layer provided between the positive electrode and the negative electrode, It is equipped with.

[0025] With the above configuration, the effective reaction area of ​​the positive electrode active material is increased at the positive electrode. This makes it possible to reduce the resistance of the battery.

[0026] In a 15th aspect of this disclosure, for example, in the battery according to the 14th aspect, the electrolyte layer may include a sulfide solid electrolyte. With the above configuration, the output characteristics of the battery can be improved.

[0027] A method for manufacturing a positive electrode according to the sixteenth aspect of this disclosure is: A method for manufacturing a positive electrode according to any one of the first to thirteen embodiments, Mixing the positive electrode active material and the carbon black, The mixture containing the positive electrode active material and the carbon black is further mixed with the solid electrolyte, Includes.

[0028] With the above configuration, carbon black can be preferentially arranged on the surface of the positive electrode active material. Therefore, carbon black tends to concentrate on the surface of the positive electrode active material. This results in a positive electrode with an increased effective reaction area of ​​the positive electrode active material. As a result, a battery with reduced resistance can be obtained.

[0029] Embodiments of the present disclosure will be described below with reference to the drawings.

[0030] (Embodiment 1) [Positive electrode] Figure 1 is a cross-sectional view showing the schematic configuration of the positive electrode 1000 in Embodiment 1.

[0031] The positive electrode 1000 comprises a mixture of positive electrode active material 110, a solid electrolyte 100, and a conductive material 140. The conductive material 140 contains carbon black 150 having an average particle size of 100 nm or less. When a cross-section of the positive electrode 1000 is observed using a scanning electron microscope (SEM), a region in which carbon black 150 is concentrated between the positive electrode active material 110 and the solid electrolyte 100 is observed.

[0032] With the above configuration, the region where carbon black 150 is concentrated between the positive electrode active material 110 and the solid electrolyte 100 facilitates the formation of electron conduction paths on the surface of the positive electrode active material 110. As a result, the effective reaction area of ​​the positive electrode active material 110 increases. This reduces the resistance of the battery.

[0033] In this disclosure, the magnification used when observing the cross-section of the positive electrode 1000 using a scanning electron microscope (SEM) is 10,000 times.

[0034] The average particle size of carbon black 150 can be measured, for example, using TEM images obtained with a transmission electron microscope (TEM). Specifically, the average particle size can be determined by calculating the average of the area circle equivalent diameter of 20 arbitrarily selected carbon black 150 particles using TEM images.

[0035] When observing the cross-section of the positive electrode 1000 using a scanning electron microscope, the area covered by the carbon black 150 on the surface of the positive electrode active material 110 may be larger than the area covered by the carbon black 150 on the surface of the solid electrolyte 100. According to the above configuration, the effective reaction area of the positive electrode active material 110 is further increased.

[0036] When observing the cross-section of the positive electrode 1000 using a scanning electron microscope, the carbon black 150 may be concentrated and present on the surface of the positive electrode active material 110. According to the above configuration, the effective reaction area of the positive electrode active material 110 is further increased.

[0037] The x obtained by the following formula (1) may satisfy 0% < x < 100%.

[0038] x = (3·c) / (4·a·b)×10 5 ···(1)

[0039] In formula (1), a is the BET (Brunauer - Emmett - Teller) specific surface area (m 2 / g) of the positive electrode active material 110. b is the average particle size (nm) of the carbon black 150. c is the ratio of the mass of the carbon black 150 to the mass of the positive electrode active material 110 contained in the positive electrode 1000. The density ρ of the carbon black 150 is 2.0 (g / cm 3 )

[0040] The value of x obtained by formula (1) is a parameter corresponding to the coverage rate of the surface of the positive electrode active material 110 by the carbon black 150. Therefore, according to the above configuration, the resistance of the battery can be reduced.

[0041] Formula (1) is derived as follows. Assume that there are n carbon blacks 150 per unit mass (1 g) of the positive electrode active material 110. The cross-sectional area (m 2) is defined as σ. At this time, the value of x obtained by Equation (1) is the cross-sectional area σ (m of carbon black 150 per unit mass (1 g) of the positive electrode active material 110 2 ) The total σt of is divided by the surface area of carbon black 150 per unit mass (1 g) of the positive electrode active material 110 (that is, the BET specific surface area a (m of the positive electrode active material 110 2 / g)) and can be obtained by converting to a percentage.

[0042] The total cross-sectional area σ (m of carbon black 150 per unit mass (1 g) of the positive electrode active material 110 2 ) The total σt is obtained using the following equation (i).

[0043] σt = σ1 + σ2 + σ3… + σn = Σσn ···(i)

[0044] In Equation (i), the cross-sectional area σ (m of carbon black 150 2 ) is obtained by the following equation (ii) using the average particle size b (nm) of carbon black 150.

[0045] σ = (b / 2)×(b / 2)×π×10 -18 ···(ii)

[0046] In Equation (i), the number n of carbon black 150 per unit mass (1 g) of the positive electrode active material 110 is the ratio c of the mass of carbon black 150 to the mass of the positive electrode active material 110 contained in the positive electrode 1000 and the known density ρ (g / cm of carbon black 150 3 ) and is obtained by the following equation (iii). v is the volume (cm per carbon black 150 3 ) is.

[0047] n = c / (ρ·v) ···(iii)

[0048] In Equation (iii), the volume v (cm of carbon black 150 3 ) is obtained by the following equation (iv) using the average particle size b (nm) of carbon black 150.

[0049] v = (4π / 3)×(b / 2) 3 ×10 -21 ···(iv)

[0050] In formula (1), x may satisfy 5% ≤ x ≤ 60%. According to the above configuration, the resistance of the battery can be further reduced.

[0051] In formula (1), x may satisfy 10% ≤ x ≤ 50%. According to the above configuration, the resistance of the battery can be further reduced.

[0052] In formula (1), x may satisfy 15% ≤ x ≤ 40%. According to the above configuration, the resistance of the battery can be further reduced.

[0053] In formula (1), a may satisfy 0 < a ≤ 1.5. According to the above configuration, it is easy to effectively arrange the carbon black 150 on the surface of the positive electrode active material 110.

[0054] The ratio of the mass of the conductive material 140 to the mass of the positive electrode active material 110 may be 0.03 or less. According to the above configuration, it is difficult for the conductive material to inhibit the lithium ion conduction between the positive electrode active material and the solid electrolyte.

[0055] (Conductive material) The conductive material 140 may contain carbon black 150 as a main component, and may further contain inevitable impurities, starting materials, by-products, decomposition products, etc. used when synthesizing the carbon black 150. In the present disclosure, "main component" means the component contained most in terms of mass ratio.

[0056] The conductive material 140 may contain 100% of the carbon black 150 in terms of the mass ratio to the whole of the conductive material 140, excluding inevitable impurities due to mixing.

[0057] Thus, the conductive material 140 may consist solely of carbon black 150.

[0058] The conductive material 140 may also contain carbon black 150 having an average particle size of 25 nm or less. With this configuration, the carbon black 150 adheres more easily to the surface of the positive electrode active material 110.

[0059] The shape of the conductive material 140 is not particularly limited. The shape of the conductive material 140 may be, for example, needle-shaped, spherical, or ellipsoidal.

[0060] The shape of the carbon black 150 contained in the conductive material 140 may be, for example, spherical or ellipsoidal. The shape of the carbon black 150 may be spherical. If the shape of the carbon black 150 is spherical or ellipsoidal, the surface of the spherical or ellipsoidal material may have an uneven surface.

[0061] Examples of carbon black 150 include acetylene black, furnace black, channel black, thermal black, and Ketjen black. Carbon black 150 may contain acetylene black or furnace black. Carbon black 150 may contain either acetylene black or furnace black. When carbon black 150 contains acetylene black, the electronic conductivity at the positive electrode can be further improved. Carbon black 150 may be acetylene black or furnace black. Carbon black 150 may be composed of acetylene black and furnace black.

[0062] (Cathode active material) As the positive electrode active material 110, materials usable as positive electrode active materials for all-solid-state lithium-ion batteries can be used. Examples of positive electrode active material 110 include LiCoO2 and LiNi x Me 1-x O2, LiLiLi x Co 1-xO2, LiNi 1 / 3 Co 1 / 3 Mn 1 / 3 Examples include O2, LiMnO2, hetero-element substituted Li-Mn spinel, lithium titanate, lithium metal phosphate, and transition metal oxides. LiNi x Me 1-x In O2, x satisfies 0.5 ≦ x < 1, and Me contains at least one selected from the group consisting of Co, Mn, and Al. LiNi x Co 1-x In O2, x satisfies 0 < x < 0.5. Examples of hetero-element substituted Li-Mn spinel include LiMn 1.5 Ni 0.5 O4, LiMn 1.5 Al 0.5 O4, LiMn 1.5 Mg 0.5 O4, LiMn 1.5 Co 0.5 O4, LiMn 1.5 Fe 0.5 O4, and LiMn 1.5 Zn 0.5 O4. Examples of lithium titanate include Li4Ti5O 12 . Examples of lithium metal phosphate include LiFePO4, LiMnPO4, LiCoPO4, and LiNiPO4. Examples of transition metal oxides include V2O5 and MoO3.

[0063] The positive electrode active material 110 may be a lithium-containing composite oxide selected from LiCoO2, LiNi x Me 1-x O2, LiNi x Co 1-x O2, LiNi 1 / 3 Co 1 / 3 Mn 1 / 3 O2, LiMnO2, hetero-element substituted Li-Mn spinel, lithium metal phosphate, etc.

[0064] When the positive electrode active material 110 is a lithium-containing composite oxide, the positive electrode active material 110 may have a layered rock salt structure. In a layered rock salt structure, the transition metal and lithium are regularly arranged to form a two-dimensional plane, thus enabling two-dimensional diffusion of lithium. Therefore, with the above configuration, the energy density of the battery can be improved.

[0065] (solid electrolyte) The solid electrolyte 100 may include at least one selected from the group consisting of sulfide solid electrolytes and halide solid electrolytes. With the above configuration, the output characteristics of the battery can be improved.

[0066] The solid electrolyte 100 may be a mixture of a sulfide solid electrolyte and a halide solid electrolyte.

[0067] Examples of sulfide solid electrolytes include Li2S-P2S5, Li2S-SiS2, Li2S-B2S3, Li2S-GeS2, and Li 3.25 Ge 0.25 P 0.75 S4, Li 10 GeP2S 12 These are some examples. In addition, sulfide solid electrolytes with an argyrodite structure, such as Li6PS5Cl, Li6PS5Br, and Li6PS5I, can be used. These sulfide solid electrolytes include LiX, Li2O, and MO q Li p MO q The following may be added. Here, X is at least one selected from the group consisting of F, Cl, Br, and I. Also, M is at least one selected from the group consisting of P, Si, Ge, B, Al, Ga, In, Fe, and Zn. p and q are natural numbers, respectively. One or more sulfide solid electrolytes selected from the above materials may be used.

[0068] With the above configuration, the ionic conductivity of the sulfide solid electrolyte can be further improved. This, in turn, can improve the charge and discharge efficiency of the battery.

[0069] Halide solid electrolytes are represented, for example, by the following compositional formula (2).

[0070] Li α M β X γ ...Equation (2)

[0071] Here, α, β, and γ are each independently greater than 0. M includes at least one element selected from the group consisting of metallic and metalloid elements other than Li. X includes at least one element selected from the group consisting of F, Cl, Br, and I.

[0072] In this disclosure, “metalloid elements” refers to B, Si, Ge, As, Sb, and Te. “Metallic elements” refers to all elements in groups 1 through 12 of the periodic table, excluding hydrogen, and all elements in groups 13 through 16 of the periodic table, excluding B, Si, Ge, As, Sb, Te, C, N, P, O, S, and Se. In other words, “metalloid elements” or “metallic elements” are the group of elements that can become cations when forming inorganic compounds with halogen elements.

[0073] The halide solid electrolyte represented by compositional formula (2) has higher ionic conductivity compared to halide solid electrolytes such as LiI, which consists of Li and halogen elements. Therefore, the halide solid electrolyte represented by compositional formula (2) can further improve the ionic conductivity of the halide solid electrolyte.

[0074] In compositional formula (2), M may be at least one element selected from the group consisting of metallic elements and metalloid elements other than Li.

[0075] In composition formula (2), X may be at least one selected from the group consisting of F, Cl, Br, and I.

[0076] The composition formula (2) may satisfy 2.5 ≤ α ≤ 3, 1 ≤ β ≤ 1.1, and γ = 6. With the above configuration, the ionic conductivity of the halide solid electrolyte can be further improved.

[0077] In compositional formula (2), M may also contain Y (=yttrium). That is, the halide solid electrolyte may contain Y as a metallic element. With the above configuration, the ionic conductivity of the halide solid electrolyte can be further improved.

[0078] A solid halogen electrolyte containing Y is, for example, Li a Me b Y c The compound may be represented by the empirical formula X6, where a+mb+3c=6 and c>0. Me is at least one element selected from the group consisting of metallic and metalloid elements, excluding Li and Y. m is the valence of element Me. X is at least one element selected from the group consisting of F, Cl, Br, and I.

[0079] Me may be, for example, 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.

[0080] With the above configuration, the ionic conductivity of the halide solid electrolyte can be further improved.

[0081] As a halide solid electrolyte, for example, the following materials can be used. The following configuration can further improve the ionic conductivity of the halide solid electrolyte.

[0082] The halide solid electrolyte may be a material represented by the following compositional formula (A1).

[0083] Li 6-3d Y d X6...Formula (A1)

[0084] In the compositional formula (A1), X is at least one selected from the group consisting of F, Cl, Br, and I. Also, 0 < d < 2 is satisfied.

[0085] The halide solid electrolyte may be a material represented by the following compositional formula (A2).

[0086] Li3YX6 ··· Formula (A2)

[0087] In the compositional formula (A2), X is at least one selected from the group consisting of F, Cl, Br, and I.

[0088] The halide solid electrolyte may be a material represented by the following compositional formula (A3).

[0089] Li 3-3δ Y 1+δ Cl6 ··· Formula (A3)

[0090] In the compositional formula (A3), 0 < δ ≦ 0.15 is satisfied. <0000​​​​​​​​​​​​​​​​​​​​​​​​​​​​​​​​​​​​​​In the composition formula (A5), Me contains at least one selected from the group consisting of Mg, Ca, Sr, Ba, and Zn. Me may be at least one selected from the group consisting of Mg, Ca, Sr, Ba, and Zn.

[0097] In the composition formula (A5), -1 < δ < 2, 0 < a < 3, 0 < (3 - 3δ + a), 0 < (1 + δ - a), 0 ≤ x ≤ 6, 0 ≤ y ≤ 6, and (x + y) ≤ 6 are satisfied.

[0098] The halide solid electrolyte may be a material represented by the following composition formula (A6).

[0099] Li 3-3δ Y 1+δ-a Me a Cl 6-x-y Br x I y ··· Formula (A6)

[0100] In the composition formula (A6), Me contains at least one selected from the group consisting of Al, Sc, Ga, and Bi. Me may be at least one selected from the group consisting of Al, Sc, Ga, and Bi.

[0101] In the composition formula (A6), -1 < δ < 1, 0 < a < 2, 0 < (1 + δ - a), 0 ≤ x ≤ 6, 0 ≤ y ≤ 6, and (x + y) ≤ 6 are satisfied.

[0102] The halide solid electrolyte may be a material represented by the following composition formula (A7).

[0103] Li 3-3δ-a Y 1+δ-a Me a Cl 6-x-y Br x I y ··· Formula (A7)

[0104] In compositional formula (A7), Me contains at least one selected from the group consisting of Zr, Hf, and Ti. Me may be at least one selected from the group consisting of Zr, Hf, and Ti.

[0105] In compositional formula (A7), -1 < δ < 1, 0 < a < 1.5, 0 < (3 - 3δ - a), 0 < (1 + δ - a), 0 ≤ x ≤ 6, 0 ≤ y ≤ 6, and (x + y) ≤ 6 are satisfied.

[0106] The halide solid electrolyte may be a material represented by the following compositional formula (A8).

[0107] Li 3-3δ-2a Y 1+δ-a Me a Cl 6-x-y Br x I y ··· Formula (A8)

[0108] In compositional formula (A8), Me contains at least one selected from the group consisting of Ta and Nb. Me may be at least one selected from the group consisting of Ta and Nb.

[0109] In compositional formula (A8), -1 < δ < 1, 0 < a < 1.2, 0 < (3 - 3δ - 2a), 0 < (1 + δ - a), 0 ≤ x ≤ 6, 0 ≤ y ≤ 6, and (x + y) ≤ 6 are satisfied.

[0110] More specifically, as the halide solid electrolyte, for example, Li3YX6, Li2MgX4, Li2FeX4, Li(Al, Ga, In)X4, Li3(Al, Ga, In)X6, etc. can be used. Here, X is at least one selected from the group consisting of F, Cl, Br, and I.

[0111] In the present disclosure, the notation "(A, B, C)" in the chemical formula means "at least one selected from the group consisting of A, B, and C". For example, "(Al, Ga, In)" is synonymous with "at least one selected from the group consisting of Al, Ga, and In". The same applies to other elements.

[0112] The halide solid electrolyte does not necessarily have to contain sulfur. With the above configuration, the generation of hydrogen sulfide gas can be suppressed. Therefore, it becomes possible to realize a battery with improved safety.

[0113] The shape of the solid electrolyte 100 is not particularly limited. The shape of the solid electrolyte 100 may be, for example, needle-shaped, spherical, or ellipsoidal. For example, the shape of the solid electrolyte 100 may be particulate.

[0114] For example, if the solid electrolyte 100 is particulate (e.g., spherical), the median diameter of the solid electrolyte 100 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 1000. This improves the charge and discharge characteristics of the battery.

[0115] The median diameter of the solid electrolyte 100 may be 10 μm or less. With the above configuration, the positive electrode active material 110 and the solid electrolyte 100 can form a good dispersion state in the positive electrode 1000.

[0116] The median diameter of the solid electrolyte 100 may be smaller than the median diameter of the positive electrode active material 110. With the above configuration, the positive electrode active material 110 and the solid electrolyte 100 can form a better dispersion state in the positive electrode 1000.

[0117] The shape of the positive electrode active material 110 is not particularly limited. The shape of the positive electrode active material 110 may be, for example, needle-shaped, spherical, or ellipsoidal. For example, the shape of the positive electrode active material 110 may be particulate.

[0118] 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, the positive electrode active material 110 and the solid electrolyte 100 can form a good dispersion state in the positive electrode 1000. This improves the charge and discharge characteristics of the battery. When the median diameter of the positive electrode active material 110 is 100 μm or less, the diffusion rate of lithium within the positive electrode active material 110 is sufficiently ensured. This allows the battery to operate at high power.

[0119] The median diameter of the positive electrode active material 110 may be larger than the median diameter of the solid electrolyte 100. This allows the positive electrode active material 110 and the solid electrolyte 100 to form a good dispersion state.

[0120] In this disclosure, median diameter means particle size (d50) when the cumulative volume in the volume-based particle size distribution is equal to 50%. The volume-based particle size distribution is measured, for example, by a laser diffraction measuring device or an image analysis device.

[0121] In the positive electrode 1000, the solid electrolyte 100 and the positive electrode active material 110 may be in contact with each other.

[0122] The positive electrode 1000 may contain a plurality of solid electrolyte 100 particles and a plurality of positive electrode active material 110 particles.

[0123] In the positive electrode 1000, the content of the solid electrolyte 100 and the content of the positive electrode active material 110 may be the same or different.

[0124] The positive electrode 1000 may contain multiple conductive materials 140.

[0125] The positive electrode 1000 may contain multiple carbon black 150 particles.

[0126] <Manufacturing method for positive electrode> The manufacturing method for the positive electrode 1000 will be explained with reference to Figure 2. Figure 2 is a flowchart showing the manufacturing method for the positive electrode 1000. The positive electrode 1000 can be manufactured by each step shown in the flowchart.

[0127] First, the positive electrode active material 110 and carbon black 150 are mixed (step S1). The positive electrode active material 110 and carbon black 150 satisfy the parameter limitations of formula (1) above. In step S1, for example, a solvent and carbon black 150 may be prepared, the carbon black 150 may be mixed with the solvent, and then the positive electrode active material 110 may be added to the resulting mixture and mixed. Next, solid electrolyte 100 is further mixed into the mixture containing the positive electrode active material 110 and carbon black 150 (step S2). This yields a slurry of positive electrode material containing a mixture of positive electrode active material 110, solid electrolyte 100, and carbon black 150. The prepared slurry is applied to a current collector and dried to obtain the positive electrode 1000.

[0128] In this embodiment, instead of mixing the positive electrode active material 110, solid electrolyte 100, and carbon black 150 all at once, the positive electrode active material 110 and carbon black 150 are mixed first. Then, the solid electrolyte 100 is further mixed into the resulting mixture. This manufacturing method allows the carbon black 150 to be preferentially arranged on the surface of the positive electrode active material 110. As a result, the carbon black 150 tends to be concentrated on the surface of the positive electrode active material 110. This results in a positive electrode 1000 with an increased effective reaction area of ​​the positive electrode active material 110. Consequently, a battery with reduced resistance can be obtained.

[0129] Even if the positive electrode active material 110 and carbon black 150 satisfy the parameter limitations of formula (1) above, the positive electrode 1000 of this disclosure cannot be obtained when the positive electrode active material 110, solid electrolyte 100, and carbon black 150 are mixed simultaneously.

[0130] The method for mixing the positive electrode active material 110 and the carbon black 150 is not particularly limited. The method for further mixing the solid electrolyte 100 into the mixture containing the positive electrode active material 110 and the carbon black 150 is also not particularly limited. For example, the positive electrode active material 110 and the carbon black 150 may be mixed using a machine such as a homogenizer. Similarly, the solid electrolyte 100 may be further mixed into the mixture containing the positive electrode active material 110 and the conductive material 140 using a machine such as a homogenizer. Using a homogenizer allows for uniform mixing. The mixing ratio of the positive electrode active material 110 and the solid electrolyte 100 is not particularly limited.

[0131] (Variation 1) Figure 3 is a cross-sectional view showing the schematic configuration of the positive electrode 1001 in Modification 1. In the positive electrode 1001, the conductive material 140 further comprises a fibrous carbon material 160. That is, in Modification 1, the conductive material 140 comprises carbon black 150 and a fibrous carbon material 160. Thus, the conductive material 140 may further comprise a fibrous carbon material 160. With the above configuration, the electronic conductivity of the positive electrode 1001 can be further improved.

[0132] Examples of fibrous carbon materials 160 include fibrous carbon such as vapor-phase carbon fibers, carbon nanotubes, and carbon nanofibers. The fibrous carbon material 160 may contain one of these materials, or two or more of these materials. The fibrous carbon material 160 may be composed of one of these materials, or two or more of these materials.

[0133] In modified example 1, the positive electrode 1001 may contain a plurality of fibrous carbon materials 160.

[0134] <Manufacturing method for positive electrode> The manufacturing method for the positive electrode 1001 will be explained with reference to Figure 4. Figure 4 is a flowchart showing the manufacturing method for the positive electrode 1001. The positive electrode 1001 can be manufactured by each step shown in the flowchart.

[0135] First, the positive electrode active material 110 and carbon black 150 are mixed (step S11). Step S11 is the same as step S1 in Figure 2. Next, the solid electrolyte 100 and fibrous carbon material 160 are further mixed into the mixture containing the positive electrode active material 110 and carbon black 150 (step S12). This yields a slurry of positive electrode material containing the mixture of positive electrode active material 110, solid electrolyte 100, carbon black 150, and fibrous carbon material 160. The prepared slurry is applied to a current collector and dried to obtain the positive electrode 1001.

[0136] (Modification 2) Figure 5 is a cross-sectional view showing the schematic configuration of the positive electrode 1002 in Modification 2. The positive electrode 1002 further comprises a coating layer 120 that covers at least a portion of the surface of the positive electrode active material 110. The positive electrode active material 110 whose surface is at least partially covered by the coating layer 120 is referred to as the "coated positive electrode active material 130". Thus, the positive electrode 1002 may further include a coating layer 120 that covers at least a portion of the surface of the positive electrode active material 110. With the above configuration, the resistance of the battery can be further reduced.

[0137] The coating layer 120 is in direct contact with the positive electrode active material 110.

[0138] Hereinafter, the material constituting the coating layer 120 will be referred to as the "coating material." The coated positive electrode active material 130 in Embodiment 2 includes the positive electrode active material 110 and the coating material. The coating material is present on at least a portion of the surface of the positive electrode active material 110 to form the coating layer 120.

[0139] The coating layer 120 may uniformly cover the positive electrode active material 110. With this configuration, the positive electrode active material 110 and the coating layer 120 are in close contact, which can further reduce the resistance of the battery.

[0140] The coating layer 120 may cover only a portion of the surface of the positive electrode active material 110. Direct contact between the particles of the positive electrode active material 110 through the portion not covered by the coating layer 120 improves the electron conductivity between the particles of the positive electrode active material 110. As a result, the battery can operate at high power.

[0141] The coating layer 120 over the positive electrode active material 110 suppresses the formation of an oxide film due to the oxidative decomposition of other solid electrolytes during battery charging. As a result, the battery's charge and discharge efficiency is improved. An example of another solid electrolyte is solid electrolyte 100.

[0142] The coating material may include Li and at least one selected from the group consisting of O, F, and Cl.

[0143] The coating material may include at least one selected from the group consisting of lithium niobate, lithium phosphate, lithium titanate, lithium tungstate, lithium zirconate fluoride, lithium aluminum fluoride, lithium titanate fluoride, and lithium magnesium fluoride.

[0144] The coating material may also be lithium niobate (LiNbO3).

[0145] <Manufacturing method for positive electrode> The positive electrode 1002 can be manufactured by replacing the positive electrode active material 110 with the coated positive electrode active material 130 in the manufacturing method of the positive electrode 1000 shown in Figure 2. The positive electrode active material 110 and carbon black 150 contained in the coated positive electrode active material 130 satisfy the parameter limitations of formula (1) above.

[0146] Here, the coated positive electrode active material 130 can be manufactured, for example, by the following method. First, a coating layer 120 is formed on the surface of the particles of the positive electrode active material 110. The method for forming the coating layer 120 is not particularly limited. Examples of methods for forming the coating layer 120 include liquid-phase coating and gas-phase coating.

[0147] For example, in the liquid-phase coating method, a precursor solution of the ion-conducting material is applied to the surface of the positive electrode active material 110. When forming a coating layer 120 containing LiNbO3, the precursor solution may be a mixed solution (sol solution) of a solvent, lithium alkoxide, and niobalkoxide. Examples of lithium alkoxides include lithium ethoxide. Examples of niobalkoxides include niobethoxide. The solvent is, for example, an alcohol such as ethanol. The amounts of lithium alkoxide and niobalkoxide are adjusted according to the target composition of the coating layer 120. Water may be added to the precursor solution as needed. The precursor solution may be acidic or alkaline.

[0148] The method for applying the precursor solution to the surface of the positive electrode active material 110 is not particularly limited. For example, the precursor solution can be applied to the surface of the positive electrode active material 110 using a rolling fluid granulation coating apparatus. With the rolling fluid granulation coating apparatus, the precursor solution can be sprayed onto the positive electrode active material 110 while rolling and fluidizing it, thereby coating the surface of the positive electrode active material 110. This forms a precursor film on the surface of the positive electrode active material 110. Subsequently, the positive electrode active material 110 coated with the precursor film is heat-treated. The heat treatment promotes gelation of the precursor film, forming a coating layer 120. This yields a coated positive electrode active material 130. At this point, the coating layer 120 covers almost the entire surface of the positive electrode active material 110. The thickness of the coating layer 120 is generally uniform.

[0149] Examples of vapor phase coating methods include pulsed laser deposition (PLD), vacuum deposition, sputtering, thermochemical vapor deposition (CVD), and plasma chemical vapor deposition. For example, in the PLD method, a high-energy pulsed laser (e.g., a KrF excimer laser, wavelength: 248 nm) is irradiated onto an ion-conducting material target, and the sublimated ion-conducting material is deposited on the surface of the positive electrode active material 110. When forming a LiNbO3 coating layer 120, high-density sintered LiNbO3 is used as the target.

[0150] (Variation 3) Figure 6 is a cross-sectional view showing the schematic configuration of the positive electrode 1003 in Modification 3. The positive electrode 1003 has the same configuration as the positive electrode 1001 in Modification 1, except that it further includes a coating layer 120 that covers at least a portion of the surface of the positive electrode active material 110. Furthermore, the positive electrode 1003 has the same configuration as the positive electrode 1002 in Modification 2, except that the conductive material 140 further includes a fibrous carbon material 160. Thus, the positive electrode 1003 may further include a coating layer 120 that covers at least a portion of the surface of the positive electrode active material 110, and the conductive material 140 may further include a fibrous carbon material 160. With the above configuration, the electronic conductivity of the positive electrode 1003 can be further improved.

[0151] In modified example 3, the positive electrode 1003 may contain multiple fibrous carbon materials 160.

[0152] <Manufacturing method for positive electrode> The positive electrode 1003 can be manufactured by replacing the positive electrode active material 110 with the coated positive electrode active material 130 in the manufacturing method of the positive electrode 1001 shown in Figure 4. The positive electrode active material 110 and carbon black 150 contained in the coated positive electrode active material 130 satisfy the parameter limitations of formula (1) above. The coated positive electrode active material 130 can be manufactured, for example, by the method described in Modification 2.

[0153] (Embodiment 2) Embodiment 2 will be described below. Descriptions that overlap with Embodiment 1 will be omitted as appropriate.

[0154] Figure 7 is a cross-sectional view showing the schematic configuration of the battery 2000 in Embodiment 2.

[0155] The battery 2000 in Embodiment 2 comprises a positive electrode 201, an electrolyte layer 202, and a negative electrode 203. The positive electrode 201 is one of the positive electrodes from Embodiment 1 and Modifications 1 to 3. The electrolyte layer 202 is disposed between the positive electrode 201 and the negative electrode 203.

[0156] With the above configuration, the effective reaction area of ​​the positive electrode active material 110 in the positive electrode 201 is increased. This makes it possible to reduce the resistance of the battery 2000.

[0157] If the positive electrode 201 is the positive electrode 1000 or positive electrode 1001 in Embodiment 1, the volume ratio "v1:100-v1" of the positive electrode active material 110 and the solid electrolyte 100 contained in the positive electrode 201 may satisfy 30≦v1≦95. Here, v1 represents the volume ratio of the positive electrode active material 110 when the total volume of the positive electrode active material 110 and the solid electrolyte 100 contained in the positive electrode 201 is set to 100. If 30≦v1 is satisfied, a sufficient energy density of the battery 2000 can be secured. If v1≦95 is satisfied, the battery 2000 can operate at high output.

[0158] If the positive electrode 201 is the positive electrode 1002 or positive electrode 1003 in Embodiment 1, the volume ratio "v11:100-v11" of the coated positive electrode active material 130 and the solid electrolyte 100 contained in the positive electrode 201 may satisfy 30 ≤ v11 ≤ 95. Here, v11 represents the volume ratio of the coated positive electrode active material 130 when the total volume of the coated positive electrode active material 130 and the solid electrolyte 100 contained in the positive electrode 201 is set to 100. If 30 ≤ v11 is satisfied, a sufficient energy density of the battery 2000 can be secured. If v11 ≤ 95 is satisfied, the battery 2000 can operate at high output.

[0159] The thickness of the positive electrode 201 may be 10 μm or more and 500 μm or less. If the thickness of the positive electrode 201 is 10 μm or more, sufficient energy density of the battery 2000 can be ensured. If the thickness of the positive electrode 201 is 500 μm or less, the battery 2000 can operate at high power.

[0160] The electrolyte layer 202 is a layer containing an electrolyte. This electrolyte is, for example, a solid electrolyte. That is, the electrolyte layer 202 may be a solid electrolyte layer. As the solid electrolyte contained in the electrolyte layer 202, the material exemplified as 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 solid electrolyte 100. With the above configuration, the charge and discharge efficiency of the battery 2000 can be further improved.

[0161] The electrolyte layer 202 may contain a halogen solid electrolyte having a composition different from that of the solid electrolyte 100.

[0162] The electrolyte layer 202 may contain a sulfide solid electrolyte.

[0163] The electrolyte layer 202 may contain only one solid electrolyte selected from the materials listed as solid electrolytes.

[0164] The electrolyte layer 202 may contain two or more solid electrolytes selected from the materials listed as solid electrolytes. In this case, the multiple solid electrolytes may have different compositions from each other. For example, the electrolyte layer 202 may contain a halide solid electrolyte and a sulfide solid electrolyte.

[0165] 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, short circuits between the positive electrode 201 and the negative electrode 203 become less likely. When the thickness of the electrolyte layer 202 is 300 μm or less, the battery 2000 can operate at high output.

[0166] The negative electrode 203 includes a material having the property of intercalating and releasing metal ions (e.g., lithium ions). The negative electrode 203 includes, for example, a negative electrode active material.

[0167] The negative electrode active material can be a metallic material, a carbon material, an oxide, a nitride, a tin compound, a silicon compound, or the like. The metallic material may be a pure metal or an alloy. Examples of metallic materials include lithium metal and lithium alloys. Examples of carbon materials include natural graphite, coke, carbon in the process of graphitization, carbon fibers, spheroidal carbon, artificial graphite, and amorphous carbon. The capacity density can be improved by using silicon (Si), tin (Sn), silicon compounds, and tin compounds.

[0168] The negative electrode 203 may contain a solid electrolyte. With the above configuration, the lithium ion conductivity inside the negative electrode 203 is increased, and the battery 2000 can operate at high power. As the solid electrolyte contained in the negative electrode 203, the material exemplified as solid electrolyte 100 in Embodiment 1 may be used. That is, the negative electrode 203 may contain a solid electrolyte having the same composition as solid electrolyte 100.

[0169] The shape of the solid electrolyte contained in the negative electrode 203 in Embodiment 2 is not particularly limited. The shape of the solid electrolyte contained in the negative electrode 203 may be, for example, needle-shaped, spherical, or ellipsoidal. For example, the shape of the solid electrolyte contained in the negative electrode 203 may be particulate.

[0170] When the solid electrolyte contained in the negative electrode 203 is particulate (for example, spherical), the median diameter of the solid electrolyte may be 100 μm or less. When the median diameter of the solid electrolyte is 100 μm or less, the negative electrode active material and the solid electrolyte can form a good dispersion state in the negative electrode 203. This improves the charge and discharge characteristics of the battery 2000.

[0171] The median diameter of the solid electrolyte contained in the negative electrode 203 may be 10 μm or less, or 1 μm or less. With the above configuration, the negative electrode active material and the solid electrolyte can form a good dispersion state in the negative electrode 203.

[0172] The median diameter of the solid electrolyte contained in the negative electrode 203 may be smaller than the median diameter of the negative electrode active material. With this configuration, the negative electrode active material and the solid electrolyte can form a better dispersion state in the negative electrode 203.

[0173] The shape of the negative electrode active material in Embodiment 2 is not particularly limited. The shape of the negative electrode active material may be, for example, needle-shaped, spherical, or ellipsoidal. For example, the shape of the negative electrode active material may be particulate.

[0174] 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 can form a good dispersion state in the negative electrode 203. This improves the charge and discharge characteristics of the battery 2000. When the median diameter of the negative electrode active material is 100 μm or less, a sufficient lithium diffusion rate is ensured within the negative electrode active material. This allows the battery 2000 to operate at high power.

[0175] The median diameter of the negative electrode active material may be larger than the median diameter of the solid electrolyte contained in the negative electrode 203. This allows the negative electrode active material and the solid electrolyte to form a good dispersion state.

[0176] The volume ratio "v2:100-v2" of the negative electrode active material and solid electrolyte contained in the negative electrode 203 may satisfy the condition 30 ≤ v2 ≤ 95. Here, v2 represents the volume ratio of the negative electrode active material when the total volume of the negative electrode active material and solid electrolyte contained in the negative electrode 203 is set to 100. If 30 ≤ v2 is satisfied, a sufficient energy density of battery 2000 can be secured. If v2 ≤ 95 is satisfied, battery 2000 can operate at high power.

[0177] 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, sufficient energy density of the battery 2000 can be ensured. When the thickness of the negative electrode 203 is 500 μm or less, the battery 2000 can operate at high power.

[0178] At least one selected from the group consisting of a positive electrode 201, an electrolyte layer 202, and a negative electrode 203 may contain a binder for the purpose of improving the adhesion between particles. The binder is used to improve the bonding properties of the materials constituting the electrode. Examples of binders include polyvinylidene fluoride, polytetrafluoroethylene, polyethylene, polypropylene, aramid resin, polyamide, polyimide, polyamideimide, polyacrylonitrile, polyacrylic acid, polymethyl polyacrylate, polyethyl polyacrylate, polyhexyl polyacrylate, polymethacrylic acid, polymethyl polymethacrylate, polyethyl polymethacrylate, polyhexyl polymethacrylate, polyvinyl acetate, polyvinylpyrrolidone, polyether, polyethersulfone, hexafluoropolypropylene, styrene-butadiene rubber, and carboxymethylcellulose. Furthermore, copolymers of two or more materials selected from the group consisting of tetrafluoroethylene, hexafluoroethylene, hexafluoropropylene, perfluoroalkyl vinyl ether, vinylidene fluoride, chlorotrifluoroethylene, ethylene, propylene, pentafluoropropylene, fluoromethyl vinyl ether, acrylic acid, and hexadiene can also be used as binders. Alternatively, a mixture of two or more materials selected from the above materials may be used as a binder.

[0179] The negative electrode 203 may contain a conductive additive to improve its electronic conductivity. Examples of conductive additives include graphites such as natural or artificial graphite, carbon blacks such as acetylene black, furnace black, and Ketjen black, conductive fibers such as carbon fibers or metal fibers, metal powders such as carbon fluoride and aluminum, conductive whiskers such as zinc oxide or potassium titanate, conductive metal oxides such as titanium oxide, and conductive polymer compounds such as polyaniline, polypyrrole, and polythiophene. Using a carbon conductive additive can reduce costs.

[0180] Examples of the shapes of the battery 2000 in Embodiment 2 include coin-shaped, cylindrical, rectangular, sheet-shaped, button-shaped, flat, and stacked types. [Examples]

[0181] Details of this disclosure will be explained below using examples and comparative examples.

[0182] First, the details of this disclosure will be explained using Examples 1 to 7 and Comparative Examples 1 to 2. In Examples 1 to 7 and Comparative Examples 1 to 2, LiNi is used as the positive electrode active material. 0.8 (Co,Mn) 0.2 O2 (hereinafter referred to as NCM) was used.

[0183] Example 1 [Preparation of sulfide solid electrolytes] In an argon glove box with a dew point of -60°C or lower, the raw material powders, Li2S and P2S5, were weighed in a molar ratio of Li2S:P2S5 = 75:25. The raw material powders were ground and mixed in a mortar to obtain a mixture. The mixture was then milled using a planetary ball mill (Fritsch, P-7 type) at 510 rpm for 10 hours. This yielded a glassy solid electrolyte. The obtained solid electrolyte was heat-treated in an inert atmosphere at 270°C for 2 hours. This produced a glass-ceramic Li2S-P2S5 (hereinafter referred to as LPS), which is a sulfide solid electrolyte.

[0184] [Fabrication of coated cathode active material] NCM was used as the positive electrode active material. LiNbO3 was used as the coating material. A coating layer containing LiNbO3 was formed by a liquid-phase coating method. Specifically, first, a precursor solution of the ion-conducting material was applied to the surface of the NCM. This formed a precursor film on the surface of the NCM. Then, the NCM coated with the precursor film was heat-treated. The heat treatment caused the gelation of the precursor film, forming a coating layer made of LiNbO3. This resulted in the acquisition of a coated positive electrode active material (hereinafter referred to as Nb-NCM). The BET specific surface area a of the fabricated Nb-NCM was 0.36 m². 2 It was / g.

[0185] [Fabrication of the positive electrode] Acetylene black with an average particle size of 23 nm was used as the conductive material. The binder, solvent, and acetylene black were mixed in an argon glove box with a dew point of -60°C or lower and dispersed using a homogenizer. This obtained a mixture of the binder, solvent, and acetylene black. Nb-NCM, a coating active material, was added to the mixture and mixed, and dispersed using a homogenizer. Subsequently, LPS, a solid electrolyte, was further added to the mixture and mixed, and dispersed using a homogenizer to prepare a slurry of positive electrode material. The mixing ratio of Nb-NCM and LPS was 70:30 by volume. The ratio c of the mass of acetylene black to the mass of Nb-NCM was 0.0030. The ratio of the total mass of the conductive material to the mass of Nb-NCM was 0.0030. The prepared slurry was applied to a current collector and dried on a hot plate to produce a positive electrode.

[0186] [Battery construction] Li2TiO3 (hereinafter referred to as LTO) was used as the negative electrode active material. In an argon glove box with a dew point of -60°C or lower, the binder, solvent, LPS, and carbon fiber (VGCF-H, manufactured by Showa Denko Corporation) were mixed and dispersed using a homogenizer. This yielded a mixture of the binder, solvent, LPS, and VGCF-H. LTO, a solid electrolyte, was added to the mixture and mixed, then dispersed using a homogenizer to prepare a slurry of the negative electrode material. The prepared slurry was applied to a current collector and dried on a hot plate to produce the negative electrode. The mixing ratio of LTO and LPS was 65:35 by volume. The ratio of the mass of VGCF-H to the mass of LTO was 0.024. "VGCF" is a registered trademark of Showa Denko Corporation.

[0187] LPS, a binder, and a solvent were mixed and dispersed using a homogenizer. This prepared an LPS-containing slurry. The prepared slurry was applied to a substrate and dried on a hot plate to create an electrolyte layer.

[0188] The fabricated negative electrode and electrolyte layer were laminated and pressure-molded while heating, after which the substrate was removed from the electrolyte layer. Next, the positive electrode was laminated on the opposite side of the resulting molded body from the negative electrode, so that the electrolyte layer and the positive electrode were in contact, and pressure-molded while heating. After attaching the current collector lead to the resulting molded body, it was placed in a laminate packaging material and the packaging material was sealed. This produced the battery of Example 1.

[0189] Example 2 In the process of preparing the positive electrode, the ratio c of the mass of acetylene black to the mass of Nb-NCM was 0.0048. Except for this, the battery of Example 2 was obtained in the same manner as in Example 1.

[0190] Example 3 In the process of preparing the positive electrode, the ratio of the mass of acetylene black to the mass of Nb-NCM was 0.0065. Aside from this, the battery of Example 2 was obtained in the same manner as in Example 1.

[0191] Example 4 In the cathode fabrication process, the ratio of the mass of acetylene black to the mass of Nb-NCM was 0.0048. Furthermore, in the cathode fabrication process, when adding and mixing LPS as a solid electrolyte, carbon fiber (VGCF-H) was added and mixed as a conductive material, and the mixture was dispersed in a homogenizer to prepare a cathode material slurry. The ratio of the mass of VGCF-H to the mass of Nb-NCM was 0.016. The ratio c of the mass of acetylene black to the mass of Nb-NCM was 0.0048. The ratio of the total mass of conductive materials to the mass of Nb-NCM was 0.0208. Except for these points, the battery of Example 4 was obtained in the same manner as in Example 1.

[0192] Example 5 In the process of fabricating the positive electrode, the ratio of the mass of VGCF-H to the mass of Nb-NCM was 0.020. The ratio c of the mass of acetylene black to the mass of Nb-NCM was 0.0013. The ratio of the total mass of conductive materials to the mass of Nb-NCM was 0.0213. Except for these factors, the battery of Example 5 was obtained in the same manner as in Example 4.

[0193] ≪Example 6≫ In the process of fabricating the positive electrode, the ratio of the mass of VGCF-H to the mass of Nb-NCM was 0.020. The ratio c of the mass of acetylene black to the mass of Nb-NCM was 0.0030. The ratio of the total mass of conductive materials to the mass of Nb-NCM was 0.0230. The battery of Example 6 was obtained in the same manner as in Example 4.

[0194] Example 7 In the process of fabricating the positive electrode, the ratio of the mass of VGCF-H to the mass of Nb-NCM was 0.020. The ratio c of the mass of acetylene black to the mass of Nb-NCM was 0.0048. The ratio of the total mass of conductive materials to the mass of Nb-NCM was 0.0248. The battery of Example 7 was obtained in the same manner as in Example 4.

[0195] ≪Comparative Example 1≫ In the process of fabricating the positive electrode, only carbon fiber (VGCF-H) was used as the conductive material. The binder, solvent, and VGCF-H were mixed in an argon glove box with a dew point of -60°C or lower and dispersed using a homogenizer. Nb-NCM, the coating active material, and LPS, the solid electrolyte, were added and mixed at once and dispersed using a homogenizer to prepare a slurry of positive electrode material. The ratio of the mass of VGCF-H to the mass of Nb-NCM was 0.008. The ratio of the total mass of the conductive material to the mass of Nb-NCM was 0.0080. A battery of Comparative Example 1 was obtained in the same manner as in Example 1, except for these points.

[0196] ≪Comparative Example 2≫ In the process of fabricating the positive electrode, the ratio of the mass of VGCF-H to the mass of Nb-NCM was 0.024. The ratio of the total mass of the conductive material to the mass of Nb-NCM was 0.0240. The battery of Comparative Example 2 was obtained in the same manner as in Comparative Example 1.

[0197] (Charge / Discharge Test) Charge and discharge tests were conducted using the batteries of Examples 1 to 7 and Comparative Examples 1 to 2 under the following conditions.

[0198] The battery was placed in a constant temperature bath at 25°C and connected to a charge / discharge device.

[0199] The battery was charged with a constant current of 2mA, which corresponds to a 0.1C rate (10-hour rate) relative to its theoretical capacity, up to a voltage of 2.7V. Then, it was charged with a constant voltage of 2.7V and terminated at a current of 0.2mA, which corresponds to a 0.01C rate. Subsequently, it was discharged with a constant current of 0.1C rate (10-hour rate) down to a voltage of 1.5V, and then discharged with a constant voltage of 1.5V down to a 0.01C rate.

[0200] Thereafter, charging was performed again under the same conditions. After constant-current discharging at a rate of 0.1C until a voltage of 2.2V, constant-voltage discharging was performed at a voltage of 2.2V until a rate of 0.01C. Furthermore, after the rest, constant-current discharging was performed at a current value of 24mA for 10 seconds. The direct current resistance of the battery calculated from the following formula (4) is described as DCR (Direct Current Resistance).

[0201] DCR = (Vo - V) × S / I ··· (4)

[0202] Here, Vo is the voltage before discharging for 10 seconds. V is the voltage after discharging for 10 seconds. S is the contact area between the positive electrode and the electrolyte layer. I is the current value, which is 24mA.

[0203] For the batteries of Examples 1 to 7 and Comparative Examples 1 to 2, the DCR ratio based on the DCR calculated by the above formula (4) is shown in Table 1 together with the value of x obtained by the above formula (1). The DCR ratio in Table 1 is a value normalized with the DCR of the battery of Comparative Example 2 as 100.

[0204]

Table 1

[0205] Next, Examples 8 to 10 and Comparative Example 3 are used to explain the details of the present disclosure. In Examples 8 to 10 and Comparative Example 3, as the positive electrode active material, LiNi 0.8 (Co,Al) 0.2 O2 (hereinafter referred to as NCA) was used.

[0206] ≪Example 8≫ In the production process of the coated positive electrode active material, NCA was used as the positive electrode active material. Except for these processes, in the same manner as in Example 1, a coated positive electrode active material (hereinafter referred to as Nb-NCA) was produced. The BET specific surface area a of the produced Nb-NCA was 0.75m 2 / g.

[0207] In the process of fabricating the positive electrode, the ratio c of the mass of acetylene black to the mass of Nb-NCA was 0.0048. The ratio of the total mass of the conductive material to the mass of Nb-NCA was 0.0048. Except for these steps, the battery of Example 8 was obtained in the same manner as in Example 1.

[0208] ≪Example 9≫ In the process of preparing the positive electrode, the ratio c of the mass of acetylene black to the mass of Nb-NCA was 0.0013. Furthermore, in the process of preparing the positive electrode, when adding and mixing LPS as a solid electrolyte, carbon fiber (VGCF-H) was added and mixed as a conductive material, and the mixture was dispersed in a homogenizer to prepare a slurry of the positive electrode material. The ratio of the mass of VGCF-H to the mass of Nb-NCA was 0.020. The ratio of the total mass of the conductive material to the mass of Nb-NCA was 0.0213. Except for these points, the battery of Example 9 was obtained in the same manner as in Example 8.

[0209] Example 10 In the process of fabricating the positive electrode, the ratio c of the mass of acetylene black to the mass of Nb-NCA was 0.0030. The ratio of the total mass of the conductive material to the mass of Nb-NCA was 0.0230. The battery of Example 10 was obtained by performing the same steps as in Example 9.

[0210] ≪Comparative Example 3≫ In the process of fabricating the positive electrode, only carbon fiber (VGCF-H) was used as the conductive material. The binder, solvent, and VGCF-H were mixed in an argon glove box with a dew point of -60°C or lower and dispersed using a homogenizer. Nb-NCA, the coating active material, and LPS, the solid electrolyte, were added and mixed at once and dispersed using a homogenizer to prepare a slurry of positive electrode material. The ratio of the mass of VGCF-H to the mass of Nb-NCA was 0.024. The ratio of the total mass of the conductive material to the mass of Nb-NCA was 0.0240. The battery of Comparative Example 3 was obtained in the same manner as in Example 8, except for these points.

[0211] (Charge / Discharge Test) Charge and discharge tests were conducted using the batteries from Examples 8 to 10 and Comparative Example 3 under the same conditions as in Examples 1 to 7 and Comparative Examples 1 to 2.

[0212] Table 2 shows the DCR ratios for the batteries of Examples 8 to 10 and Comparative Example 3, based on the DCR calculated by formula (4) above, along with the value of x obtained by formula (1) above. The DCR ratios in Table 2 are normalized values ​​with the DCR of the battery of Comparative Example 3 set to 100.

[0213] [Table 2]

[0214] ≪Consideration≫ The results shown in Tables 1 and 2 indicate that when carbon black is preferentially placed on the surface of the positive electrode active material using the positive electrode manufacturing method according to this disclosure, the DCR ratio decreases. This is thought to be because the number of electron conduction paths formed on the surface of the positive electrode active material increases, thereby increasing the effective reaction area of ​​the positive electrode active material.

[0215] As shown in Examples 1 to 10, when the value of x obtained by formula (1) satisfies 5% ≤ x ≤ 60%, the DCR ratio was low and lithium ion conduction between the positive electrode active material and the solid electrolyte was smooth.

[0216] (Cross-sectional observation of the positive electrode) Figure 8 shows a cross-sectional SEM image of the positive electrode of Example 1, obtained using a scanning electron microscope. The magnification was 10,000x. According to the positive electrode fabrication method described above, carbon black could be preferentially arranged on the surface of the positive electrode active material. Therefore, when the cross-section of the positive electrode was observed using a scanning electron microscope, a region in which carbon black was concentrated between the positive electrode active material and the solid electrolyte was observed. Specifically, the area covered by carbon black on the surface of the positive electrode active material was larger than the area covered by carbon black on the surface of the solid electrolyte. Similar results were observed in the other examples as well. [Industrial applicability]

[0217] The battery described herein can be used, for example, as an all-solid-state lithium secondary battery. [Explanation of symbols]

[0218] 1000,1001,1002,1003 Positive electrode 100 solid electrolyte 110 Cathode active material 120 Covering layer 130 Coated positive electrode active material 140 Conductive materials 150 Carbon Black 160 Fibrous carbon materials 2000 batteries 201 Positive electrode 202 Electrolyte layer 203 Negative electrode

Claims

1. A positive electrode comprising a mixture of a positive electrode active material, a solid electrolyte, and a conductive material, The conductive material includes carbon black having an average particle size of 100 nm or less. When the cross-section of the positive electrode is observed using a scanning electron microscope, the area of ​​the positive electrode active material covered by the carbon black is larger than the area of ​​the solid electrolyte covered by the carbon black. Positive electrode.

2. The value of x obtained by the following equation (1) satisfies 0% < x < 100%, x=(3・c) / (4・a・b)×10 5 ・・・(1) In formula (1) above, a is the BET (Brunauer-Emmett-Teller) specific surface area (m²) of the positive electrode active material. 2 The density of the carbon black is 2.0 (g / cm³), where b is the average particle size (nm) of the carbon black, c is the ratio of the mass of the carbon black to the mass of the positive electrode active material contained in the positive electrode, and the density of the carbon black is 2.0 (g / cm³). 3 ) The positive electrode according to claim 1.

3. In the above formula (1), x satisfies 5% ≤ x ≤ 60%. The positive electrode according to claim 2.

4. In the above formula (1), x satisfies 10% ≤ x ≤ 50%. The positive electrode according to claim 2.

5. In the above formula (1), x satisfies 15% ≤ x ≤ 40%. The positive electrode according to claim 2.

6. In the above formula (1), a satisfies 0 < a ≤ 1.

5. The positive electrode according to claim 2.

7. The conductive material further comprises a fibrous carbon material. The positive electrode according to claim 1.

8. The ratio of the mass of the conductive material to the mass of the positive electrode active material is 0.03 or less. The positive electrode according to claim 1.

9. The carbon black has an average particle size of 25 nm or less. The positive electrode according to claim 1.

10. The carbon black includes acetylene black. The positive electrode according to claim 1.

11. The solid electrolyte includes at least one selected from the group consisting of sulfide solid electrolytes and halide solid electrolytes. The positive electrode according to claim 1.

12. The positive electrode active material has a layered rock salt structure. The positive electrode according to claim 1.

13. The coating further comprises a coating layer that covers at least a portion of the surface of the positive electrode active material. The positive electrode according to claim 1.

14. A positive electrode according to any one of claims 1 to 13, The negative electrode and, An electrolyte layer disposed between the positive electrode and the negative electrode, Equipped with, battery.

15. The electrolyte layer contains a sulfide solid electrolyte. The battery according to claim 14.

16. A method for manufacturing a positive electrode according to any one of claims 1 to 13, Mixing the positive electrode active material and the carbon black, The mixture containing the positive electrode active material and the carbon black is further mixed with the solid electrolyte, including, A method for manufacturing a positive electrode.

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