Patent Application
20240282944
This nonprovisional application is based on Japanese Patent Application No. 2023-021504 filed on Feb. 15, 2023, with the Japan Patent Office, the entire contents of which are hereby incorporated by reference.
The present disclosure relates to a lithium metal negative electrode secondary battery.
Japanese Patent Laying-Open No. 2021-166195 discloses forming a layer that includes lithium phosphate, on the surface of a negative electrode current collector.
Generally, at a negative electrode of a lithium (Li) ion secondary battery, an insertion reaction takes place. The insertion reaction refers to a reaction of Li ions moving in and out of crystals of a host material (such as graphite, for example).
At a negative electrode of a Li metal negative electrode secondary battery, a dissolution/deposition reaction takes place. More specifically, during charging, Li metal becomes deposited from the electrolyte solution. During discharging, Li metal dissolves into the electrolyte solution. Due to the dissolution/deposition reaction, energy density is expected to be increased. However, there is still some room for improvement in cycle endurance of Li metal negative electrode secondary batteries.
An object of the present disclosure is to improve cycle endurance of Li metal negative electrode secondary batteries.
Hereinafter, the technical configuration and effects of the present disclosure will be described. It should be noted that the action mechanism according to the present specification includes presumption. The action mechanism does not limit the technical scope of the present disclosure.
1. A lithium metal negative electrode secondary battery comprises a positive electrode, a separator, a negative electrode, and an electrolyte solution. The electrolyte solution includes lithium ions. The separator is interposed between the positive electrode and the negative electrode. The negative electrode includes a negative electrode base material and a lithium metal layer. The lithium metal layer includes a continuous phase and a dispersed phase. The continuous phase includes lithium metal. The dispersed phase includes a lithium-ion conductor. The lithium-ion conductor has a lithium-ion conductivity from 1.0×10−13 to 2.0×10−9 S/cm.
Conventionally, in a Li metal negative electrode secondary battery, during charging, Li metal may become deposited non-uniformly. As a result of repeated charge and discharge (repeated dissolution and deposition), non-uniformity of Li metal may be increased. For example, Japanese Patent Laying-Open No. 2021-166195 suggests forming a protective layer on the surface of a negative electrode base material. The protective layer includes lithium phosphate (Li3PO4). Japanese Patent Laying-Open No. 2021-166195 states that due to the presence of the protective layer, the deposition of Li metal becomes uniform.
However, the presence of the protective layer may also facilitate capacity degradation. Li ions move through the protective layer to reach the surface of the negative electrode base material. At the surface of the negative electrode base material, Li ions receive electrons and thereby Li metal becomes deposited. The Li metal may form a Li metal layer. As the Li metal becomes deposited (as charging proceeds), the Li metal layer may become thicker. The Li metal layer thus grows and pushes up the protective layer, and thereby a three-layer structure is formed. The resulting three-layer structure includes the negative electrode base material, the Li metal layer, and the protective layer in this order. In the three-layer structure ((negative electrode base material)/(Li metal layer)/(protective layer)), the protective layer may inhibit contact between the Li metal layer and the electrolyte solution. As a result, the Li metal layer may not be sufficiently impregnated with the electrolyte solution. With the insufficient impregnation with the electrolyte solution, electric charge carriers (Li ions) are not easily transported to the interface between the negative electrode base material and the Li metal layer. Due to the insufficient supply of Li ions, the size of Li metal deposition becomes small. Due to the small size of Li metal deposition, at the interface between the Li metal layer and the negative electrode base material, a side reaction between Li metal and the electrolyte solution may be facilitated. As a result, peel strength between the Li metal layer and the negative electrode base material may be impaired. When peeling occurs at the interface between the Li metal layer and the negative electrode base material, capacity degradation may proceed rapidly.
Usually, Li3PO4 in the protective layer according to Japanese Patent Laying-Open No. 2021-166195 has a Li-ion conductivity of about 1.0×10−7 S/cm. In the present disclosure, a Li-ion conductor with a markedly lower Li-ion conductivity is used. More specifically, the Li-ion conductivity of the Li-ion conductor is 2.0×10−9 S/cm or less.
Based on conventional findings, it is conjectured that the presence of a Li-ion conductor with a low Li-ion conductivity on the surface of the negative electrode base material inhibits Li-ion movement and thereby facilitates capacity degradation. However, according to a novel finding of the present disclosure, when the Li-ion conductivity is 2.0×10−9 S/cm or less, the state of Li metal deposition may change and capacity degradation may be reduced. More specifically, the Li metal layer may grow with the Li-ion conductor trapped therein. Inside the Li metal layer, Li metal forms a continuous phase and the Li-ion conductor forms a dispersed phase. Inside the Li metal layer, mobility of Li ions at the interface of the three phases, namely the Li metal, the Li-ion conductor, and the electrolyte solution may be increased. This may facilitate Li-ion supply to the interface between the Li metal layer and the negative electrode base material. As a result, at the interface between the Li metal layer and the negative electrode base material, occurrence of side reaction between Li metal and the electrolyte solution may become less frequent. With the peel strength between the Li metal layer and the negative electrode base material being maintained, capacity degradation is expected to be reduced. That is, cycle endurance is expected to be improved.
It should be noted that when the Li-ion conductivity is below 1.0×10−13 S/cm, Li-ion movement may be excessively inhibited and thereby capacity degradation may be facilitated. Hence, the Li-ion conductivity is equal to or more than 1.0×10−13 S/cm.
2. The lithium metal negative electrode secondary battery according to “1” above may include the configuration described below, for example. The lithium-ion conductor includes a first component, a second component, and a third component.
The first component is Li.
The second component is at least one selected from the group consisting of Mg, Al, Ti, Zn, Zr, Nb, Mo, Ta, W, and a rare earth element.
The third component is at least one selected from the group consisting of B, N, O, Si, P, S, Ge, and a halogen.
3. The lithium metal negative electrode secondary battery according to “1” or “2” above may include the configuration described below, for example. The dispersed phase further includes a binder. The volume fraction of the binder relative to a sum of the lithium-ion conductor and the binder is less than 0.2.
With the volume fraction of the binder being less than 0.2, trapping of the Li-ion conductor into the Li metal layer tends to be facilitated.
4. The lithium metal negative electrode secondary battery according to any one of “1” to “3” above may include the configuration described below, for example. The lithium metal negative electrode secondary battery satisfies a relationship of the following expression (1-1).
In the above expression (1-1), each of A0 and A1 is a value measured at an SOC of 100%. A0 represents an area of a cross section of the lithium metal layer occupied by the lithium metal. A1 represents an area of the cross section of the lithium metal layer occupied by the lithium-ion conductor.
Hereinafter, “A1/A0” in the above expression (1-1) is also called “the presence ratio of the Li-ion conductor”. When the presence ratio of the Li-ion conductor is from 0.1 to 0.5 (from 10 to 50%), cycle endurance is expected to be improved.
5. The lithium metal negative electrode secondary battery according to any one of “1” to “4” above may include the configuration described below, for example. The lithium-ion conductor includes lithium phosphate.
As described above, usually, Li3PO4 may have a Li-ion conductivity of about 1.0×10−7 S/cm. In the present disclosure, the Li-ion conductivity of Li3PO4 may be adjusted to 2.0×10−9 S/cm or less by subjecting Li3PO4 to, for example, a treatment that causes disturbance in the crystallinity of the particle surface.
6. The lithium metal negative electrode secondary battery according to any one of “1” to “5” above may be an anode-free battery, for example.
With the lithium metal negative electrode secondary battery being an anode-free battery, energy density is expected to be enhanced, for example.
Next, an embodiment of the present disclosure (which may also be simply called “the present embodiment” hereinafter) and an example of the present disclosure (which may also be simply called “the present example” hereinafter) will be described. It should be noted that neither the present embodiment nor the present example limits the technical scope of the present disclosure. The present embodiment and the present example are illustrative in any respect. The present embodiment and the present example are non-restrictive. The technical scope of the present disclosure encompasses any modifications within the meaning and the scope equivalent to the terms of the claims. For example, it is originally planned that certain configurations of the present embodiment and the present example can be optionally combined.
The foregoing and other objects, features, aspects and advantages of the present disclosure will become more apparent from the following detailed description of the present disclosure when taken in conjunction with the accompanying drawings.
A description will be provided for terms that are used in the present specification. Terms that are not described here may be described in the specification when the term is used.
Expressions such as “comprise”, “include”, and “have”, and other similar expressions (such as “be composed of”, for example) are open-ended expressions. In an open-ended expression, in addition to an essential component, an additional component may or may not be further included. The expression “consist of” is a closed-end expression. However, even when a closed-end expression is used, impurities present under ordinary circumstances as well as an additional element irrelevant to the technique according to the present disclosure are not excluded. The expression “consist essentially of” is a semiclosed-end expression. A semiclosed-end expression tolerates addition of an element that does not substantially affect the fundamental, novel features of the technique according to the present disclosure.
Expressions such as “may” and “can” are not intended to mean “must” (obligation) but rather mean “there is a possibility” (tolerance).
A singular form also includes its plural meaning, unless otherwise specified. For example, “a particle” may mean not only “one particle” but also “a plurality of particles (a particle group)” and “a group of particles (powder)”.
A numerical range such as “from m to n %” includes both the upper limit and the lower limit, unless otherwise specified. That is, “from m to n %” means a numerical range of “not less than m % and not more than n %”. Moreover, “not less than m % and not more than n %” includes “more than m % and less than n %”. “Not less than” and “not more than” are represented by an inequality symbol with an equality symbol, e.g., “≤”. “More than” and “less than” are represented by an inequality symbol without an equality symbol, e.g., “<”. Any numerical value selected from a certain numerical range may be used as a new upper limit or a new lower limit. For example, any numerical value from a certain numerical range may be combined with any numerical value described in another location of the present specification or in a table or a drawing to set a new numerical range.
All the numerical values are regarded as being modified by the term “about”. The term “about” may mean ±5%, ±3%, ±1%, and/or the like, for example. Each numerical value may be an approximate value that can vary depending on the implementation configuration of the technique according to the present disclosure. Each numerical value may be expressed in significant figures. Unless otherwise specified, each measured value may be the average value obtained from multiple measurements performed. The number of measurements may be 3 or more, or may be 5 or more, or may be 10 or more. Generally, the greater the number of measurements is, the more reliable the average value is expected to be. Each measured value may be rounded off based on the number of the significant figures. Each measured value may include an error occurring due to an identification limit of the measurement apparatus, for example.
A stoichiometric composition formula represents a typical example of a compound. A compound may have a non-stoichiometric composition. For example, “Al2O3” is not limited to a compound where the ratio of the amount of substance (molar ratio) is “Al/O=2/3”. “Al2O3” represents a compound that includes Al and O in any composition ratio, unless otherwise specified. For example, the compound may be doped with a trace element. Some of Al and/or O may be replaced by another element.
“Derivative” refers to a compound that is derived from its original compound by at least one partial modification selected from the group consisting of substituent introduction, atom replacement, oxidation, reduction, and other chemical reactions. The position of modification may be one position, or may be a plurality of positions. “Substituent” may include, for example, at least one selected from the group consisting of alkyl group, alkenyl group, alkynyl group, cycloalkyl group, unsaturated cycloalkyl group, aromatic group, heterocyclic group, halogen atom (F, Cl, Br, I, etc.), OH group, SH group, CN group, SCN group, OCN group, nitro group, alkoxy group, unsaturated alkoxy group, amino group, alkylamino group, dialkylamino group, aryloxy group, acyl group, alkoxycarbonyl group, acyloxy group, aryloxycarbonyl group, acylamino group, alkoxycarbonylamino group, aryloxy carbonylamino group, sulfonylamino group, sulfamoyl group, carbamoyl group, alkylthio group, arylthio group, sulfonyl group, sulfinyl group, ureido group, phosphoramide group, sulfo group, carboxy group, hydroxamic acid group, sulfino group, hydrazino group, imino group, silyl group, and the like. These substituents may be further substituted. When there are two or more substituents, these substituents may be the same as one another or may be different from each other. A plurality of substituents may be bonded together to form a ring. A derivative of a polymer compound (a resin material) may also be called “a modified product”.
“Copolymer” includes at least one selected from the group consisting of unspecified-type, statistical-type, random-type, alternating-type, periodic-type, block-type, and graft-type.
“SOC (state of charge)” refers to the percentage of the charged capacity of the battery at a particular point in time relative to the full charge capacity of the battery.
“Lithium metal negative electrode secondary battery” refers to a battery in which negative electrode reaction includes Li metal dissolution/deposition reaction. For example, Li metal dissolution/deposition reaction may be responsible for 1 to 100%, or 25 to 100%, or 50 to 100%, or 75 to 100% of the negative electrode capacity. The negative electrode capacity exhibits reversible capacity loss. For example, at an SOC from 1 to 100%, or from 1 to 75%, or from 1 to 50%, or from 1 to 25%, Li metal may be deposited on the negative electrode. At an SOC of 0% (at a fully discharged state), Li metal may be fully dissolved in the electrolyte solution. At an SOC of 0%, Li metal may partially remain at the negative electrode. Even when Li metal is fully dissolved at an SOC of 0%, as long as a Li metal layer can be formed at an SOC above 0%, it is regarded that the negative electrode includes a Li metal layer.
In the case when the Li metal layer includes a dispersed phase (a Li-ion conductor) at an SOC of 100%, it is regarded that the Li metal layer includes a dispersed phase. The description of “1” above that reads “The lithium metal layer includes a continuous phase and a dispersed phase.” may be interpreted as “The lithium metal negative electrode secondary battery is configured in such a manner that the lithium metal layer includes a continuous phase and a dispersed phase at an SOC of 100%.”, for example.
Usually, Li metal deposition in a Li-ion secondary battery may cause irreversible capacity loss. For example, Li metal deposition in a Li-ion secondary battery is an unintended reaction. For example, Li metal deposition in a Li-ion secondary battery may occur under abnormal conditions, at the time of improper use, and/or the like.
In “an anode-free battery”, no Li metal is present at the negative electrode before initial charging (after assembly and before first-time charging). An anode-free battery is assembled in a state where the negative electrode does not include Li metal (a negative electrode active material). At the time of initial charging, Li is supplied from the positive electrode to the negative electrode, and thereby, for the first time, Li metal becomes deposited on the negative electrode. In an anode-free battery, at a fully discharged state, Li metal may be fully dissolved.
“Li-ion conductivity” is measured by the procedure described below.
“Presence ratio of the Li-ion conductor” is measured by the procedure described below. The SOC of the Li metal negative electrode secondary battery is adjusted to 100%. At an SOC of 100%, the Li metal negative electrode secondary battery is disassembled and the negative electrode is collected. A cross section of the Li metal layer is exposed, and thus a sample is prepared. The resulting sample includes a cross section parallel to the thickness direction of the Li metal layer. By SEM-EDS (Scanning Electron Microscope Energy Dispersive x-ray Spectroscopy), elemental mapping analysis of the cross section of the Li metal layer is carried out. For example, the region subjected to analysis (the analysis region) is rectangular. For example, the analysis region may be defined so as to include the interface between the Li metal layer and a negative electrode base material as well as the surface of the Li metal layer. Within an elemental mapping image, from the number of pixels attributable to Li metal, the area occupied by Li metal (A0) is determined. Within the elemental mapping image, from the number of pixels attributable to the Li-ion conductor, the area occupied by the Li-ion conductor (A1) is determined. A1 is divided by A0, and thereby the presence ratio of the Li-ion conductor (A1/A0) is determined. The presence ratio is a dimensionless amount. The presence ratio may be expressed in percentage.
The description of “4” above that reads “The lithium metal negative electrode secondary battery satisfies a relationship of the expression (1-1).” may be interpreted as “The lithium metal negative electrode secondary battery is configured in such a manner that the relationship of the expression (1-1) is satisfied at an SOC of 100%.”, for example.
“Average particle size” refers to a particle size in volume-based particle size distribution (cumulative distribution) at which the cumulative value reaches 50%. The particle size may also be called “D50”. The average particle size may be measured by laser diffraction.
Battery 100 may include an exterior package (not illustrated). The exterior package may accommodate power generation element 50 and an electrolyte solution. The exterior package may have any configuration. The exterior package may be a case made of metal, or may be a pouch made of a metal foil laminated film, for example. The case may have any shape. The case may be cylindrical, prismatic, flat, coin-shaped, and/or the like, for example. The exterior package may include Al and/or the like, for example. The exterior package may accommodate a single power generation element 50, or may accommodate a plurality of power generation elements 50, for example. The plurality of power generation elements 50 may form a series circuit, or may form a parallel circuit, for example. Inside the exterior package, the plurality of power generation elements 50 may be stacked in the thickness direction of battery 100.
Power generation element 50 includes a positive electrode 10, a negative electrode 20, and a separator 30. Separator 30 is interposed between positive electrode 10 and negative electrode 20. Power generation element 50 may have any configuration. For example, power generation element 50 may be a stack-type one. For example, positive electrode 10 and negative electrode 20 may be alternately stacked with separator 30 interposed between positive electrode 10 and negative electrode 20 to form power generation element 50. For example, separator 30 having a belt-like shape may be folded into a Z-shape, and at each turn of separator 30, positive electrode 10 and negative electrode 20 may be placed alternately. For example, power generation element 50 may be a wound-type one. For example, each of positive electrode 10, negative electrode 20, and separator 30 may have a belt-like shape. For example, positive electrode 10, separator 30, and negative electrode 20 may be stacked in this order to form a stack. The resulting stack may be wound spirally to form power generation element 50. After being wound, the wound power generation element 50 may be shaped into a flat form.
Negative electrode 20 includes a negative electrode base material 21 and a Li metal layer 22. Negative electrode base material 21 may serve as a place for Li metal deposition. Negative electrode base material 21 is electrically conductive. Negative electrode base material 21 may function as a current collector. Negative electrode base material 21 may have a thickness from 5 to 50 μm, for example. Negative electrode base material 21 may include a metal foil, a metal porous body, and/or the like, for example. Negative electrode base material 21 may include at least one selected from the group consisting of Cu, Ni, Fe, Zn, Pb, Ag, and Au, for example. Negative electrode base material 21 may include a Cu foil, a Cu alloy foil, and/or the like, for example.
Along with the increase and decrease of SOC, the thickness of Li metal layer 22 also increases or decreases. Li metal layer 22 includes a continuous phase 22a and a dispersed phase 22b. Continuous phase 22a includes Li metal. Dispersed phase 22b includes a Li-ion conductor. With dispersed phase 22b including a Li-ion conductor, cycle endurance is expected to be improved.
Dispersed phase 22b is dispersed in continuous phase 22a. The average distance between dispersed phases 22b may be from 1 to 10 μm, for example. The average distance between dispersed phases 22b may be measured in a cross-sectional image of Li metal layer 22, for example. Dispersed phase 22b may consist of a single particle, or may include aggregated particles (a plurality of particles). The Feret diameter of dispersed phase 22b may be from 0.1 to 5 μm, or from 0.5 to 3 μm, or from 1 to 3 μm, for example. The Feret diameter of dispersed phase 22b refers to the distance between two points located farthest apart from each other on the outline of dispersed phase 22b in a cross-sectional image of Li metal layer 22.
As long as dispersed phase 22b is distributed inside Li metal layer 22, part of the Li-ion conductor may be distributed outside Li metal layer 22. For example, part of the Li-ion conductor may be distributed between Li metal layer 22 and negative electrode base material 21.
The presence ratio of the Li-ion conductor may be from 0.05 to 0.6 (from 5 to 60%), or from 0.1 to 0.5 (from 10 to 50%), for example. With the presence ratio of the Li-ion conductor being from 0.1 to 0.5, cycle endurance is expected to be improved. The presence ratio of the Li-ion conductor may be 0.2 or more, or 0.3 or more, or 0.4 or more, for example. The presence ratio of the Li-ion conductor may be 0.4 or less, or 0.3 or less, or 0.2 or less, for example.
Dispersed phase 22b may further include a binder. The volume fraction of the binder relative to the sum of the Li-ion conductor and the binder may be less than 0.2 (less than 20%), for example. That is, dispersed phase 22b may include the binder in a volume fraction of less than 20%, with the remainder being made up of the Li-ion conductor. With the volume fraction of the binder being less than 0.2, dispersed phase 22b tends to be formed. The volume fraction of the binder may be expressed in percentage. The volume fraction of the binder may be 0.19 or less, or 0.15 or less, or 0.1 or less, or 0.05 or less, or 0.03 or less, or 0.01 or less, for example. The volume fraction of the binder may be 0.001 or more, or 0.005 or more, or 0.01 or more, or 0.03 or more, or 0.05 or more, or 0.1 or more, or 0.15 or more, or 0.19 or more, for example.
The binder may include any component. The binder may include a material that may be swollen with the electrolyte solution, for example. With the binder becoming swollen, formation of dispersed phase 22b may be facilitated. The binder may include, for example, at least one selected from the group consisting of polyvinylidene difluoride (PVDF), vinylidene difluoride-hexafluoropropylene copolymer (PVDF-HFP), polytetrafluoroethylene (PTFE), carboxymethylcellulose (CMC), polyacrylic acid (PAA), polyvinyl alcohol (PVA), polyvinylpyrrolidone (PVP), polyoxyethylene alkyl ether, styrene-butadiene rubber (SBR), acrylate butadiene rubber (ABR), polyacrylonitrile (PAN), and derivatives of these.
The Li-ion conductor has a Li-ion conductivity of 1.0×10−13 to 2.0×10−9 S/cm. With the Li-ion conductivity being from 1.0×10−13 to 2.0×10−9 S/cm, cycle endurance is expected to be improved. The Li-ion conductivity may be 1.0×10−12 S/cm or more, or 1.0×10−11 S/cm or more, or 1.0×10−10 S/cm or more, for example. The Li-ion conductivity may be 1.0×10−10 S/cm or less, or 1.0×10−11 S/cm or less, or 1.0×10−12 S/cm or less, for example.
The Li-ion conductor is solid. The Li-ion conductor may be a particle group. The Li-ion conductor may have an average particle size from 100 to 3000 nm (from 0.1 to 3 μm), or from 200 to 2000 nm, or from 300 to 1500 nm, for example. The average particle size of the Li-ion conductor may be 500 nm or more, or 1000 nm or more, or 1300 nm or more, for example. The average particle size of the Li-ion conductor may be 1300 nm or less, or 1000 nm or less, or 500 nm or less, for example.
As long as having a Li-ion conductivity of 1.0×10−13 to 2.0×10−9 S/cm, the Li-ion conductor may have any composition. The Li-ion conductor may include a first component, a second component, and a third component, for example. The first component is Li.
The second component is at least one selected from the group consisting of Mg, Al, Ti, Zn, Zr, Nb, Mo, Ta, W, and a rare earth element. The “rare earth element” may include lanthanoid, for example. The rare earth element may include, for example, at least one selected from the group consisting of Sc, Y, La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu.
The third component is at least one selected from the group consisting of B, N, O, Si, P, S, Ge, and a halogen. The “halogen” may include, for example, at least one selected from the group consisting of F, Cl, Br, and I.
The Li-ion conductor may include a phosphoric acid compound, for example. The Li-ion conductor may include Li3PO4, for example.
The Li-ion conductor may include a nitride phosphate compound (LIPON), for example. The Li-ion conductor may have a composition of the following formula (1-3), for example.
In the above formula (1-3), x may satisfy the relationship of 2≤x<3, for example. y may satisfy the relationship of 3≤y<4, for example. z may satisfy the relationship of 0.1<z<0.5, for example.
The Li-ion conductor may be of NASICON type, for example. The Li-ion conductor may have a composition of the following formula (1-4), for example.
In the above formula (1-4), M is at least one selected from the group consisting of Ti and Ge. x satisfies the relationship of 0≤x≤2.
The Li-ion conductor may have a composition of the following formula (1-5), for example.
In the above formula (1-5), M is at least one selected from the group consisting of Ti and Ge. x satisfies the relationship of 0.3≤x≤0.4.
The Li-ion conductor may include a composite oxide, for example. The Li-ion conductor may include at least one selected from the group consisting of LiNbO3, Li2WO4, Li3BO3, LiBO2, Li2SO4, LizSO3, LizTiO3, LizTi2O5, Li2MOO4, Li2ZrO3, and LiAlO2, for example.
The Li-ion conductor may include a garnet-type oxide, for example. The Li-ion conductor may have a composition of the following formula (1-6), for example.
In the above formula (1-6), M1 is a rare earth element. M1 may be La, for example. M2 is at least one selected from the group consisting of Mg, Nb, and Ta, for example. x may satisfy the relationship of O≤x≤1, for example. y may satisfy the relationship of O≤y≤1, for example.
The Li-ion conductor may include a perovskite-type oxide, for example. The Li-ion conductor may have a composition of the following formula (1-7), for example.
In the above formula (1-7), x may satisfy the relationship of 0<x<0.66, for example.
The Li-ion conductor may have a composition of the following formula (1-8), for example.
In the above formula (1-8), x may satisfy the relationship of 0<x<0.33, for example.
The Li-ion conductor may include an inverted-perovskite-type compound, for example. The Li-ion conductor may have a composition of the following formula (1-9), for example.
In the above formula (1-9), x may satisfy the relationship of 0≤x≤1, for example.
The Li-ion conductor may be of LISICON type, for example. The Li-ion conductor may have a composition of the following formula (1-10), for example.
In the above formula (1-10), x may satisfy the relationship of −0.36<x<0.87, for example.
The Li-ion conductor may include an oxide glass, for example. The oxide glass may be glass ceramic (partially crystallized glass). The glass may be a solid solution. For example, the composition of the glass may be expressed as its raw material composition. For example, “Li2O—Al2O3—SiO2—P2O5—TiO2” represents a material produced by mixing Li2O, Al2O3, SiO2, P2O5, and TiO2 in a freely-selected molar ratio. The mixing ratio may be expressed with the number placed in front of each raw material. For example, “50Li4SiO4-50Li3BO3” means that the mixing ratio is “Li4SiO4/Li3BO3=50/50 (molar ratio)”. The raw material of the glass may include at least one selected from the group consisting of Li2O, Al2O3, SiO2, P2O5, TiO2, Li2SO4, Li3BO3, Li3BO4, Li4SiO4, and Li3PO4, for example. The Li-ion conductor may include at least one selected from the group consisting of Li2O—Al2O3—SiO2—P2O5—TiO2, LizSO4—Li3BO3, Li3BO4—Li4SiO4, and Li3PO4—Li3BO3, for example.
The Li-ion conductor may include a sulfide, a halide, and/or the like, for example. The sulfide may be glass, glass ceramic, argyrodite, and/or the like, for example. The Li-ion conductor may include at least one selected from the group consisting of Li10GeP2S12, Li7P3S11, Li3.25Ge0.25P0.75S4, Li3.25P0.95S4, Li6PS5Cl, LiI, B2S3, Li2S, and Si2S2, for example. The Li-ion conductor may include at least one selected from the group consisting of Li2S—B2S3—LiI, Li2S—Si2S2-Lil, and Li2S—Si2S2—Li4SiO4, for example.
The Li-ion conductor may include at least one selected from the materials listed in
Usually, the Li-ion conductor having the composition described above has a Li-ion conductivity of 10−5 S/cm or more. In order to achieve a Li-ion conductivity from 1.0×10−13 to 2.0×10−9 S/cm, the Li-ion conductivity is reduced. For example, the Li-ion conductor may be subjected to pulverization treatment and sintering treatment that are repeated alternately. The pulverization treatment may be carried out with a mechanochemical apparatus and/or the like, for example. The sintering treatment may be carried out at a low temperature. The sintering temperature may be about 200° C., for example.
Positive electrode 10 may be in sheet form, for example. Positive electrode 10 may include a positive electrode base material 11 and a positive electrode active material layer 12, for example. Positive electrode base material 11 is electrically conductive. Positive electrode base material 11 may function as a current collector. Positive electrode base material 11 supports positive electrode active material layer 12. Positive electrode base material 11 may be in sheet form, for example. Positive electrode base material 11 may have a thickness from 5 to 50 μm, for example. Positive electrode base material 11 may include a metal foil, for example. Positive electrode base material 11 may include at least one selected from the group consisting of Al, Mn, Ti, Fe, and Cr, for example. Positive electrode base material 11 may include an Al foil, an Al alloy foil, a Ti foil, an SUS foil, and/or the like, for example.
Between positive electrode base material 11 and positive electrode active material layer 12, an intermediate layer (not illustrated) may be formed. The intermediate layer does not include a positive electrode active material. The intermediate layer may have a thickness from 0.1 to 5 μm, for example. The intermediate layer may include a conductive material, an insulation material, a binder, and/or the like, for example. The conductive material and the binder are described below. The insulation material may include alumina, boehmite, aluminum hydroxide, and/or the like, for example.
Positive electrode active material layer 12 is placed on the surface of positive electrode base material 11. Positive electrode active material layer 12 may be placed on only one side of positive electrode base material 11. Positive electrode active material layer 12 may be placed on both sides of positive electrode base material 11. Positive electrode active material layer 12 may have a thickness from 10 to 1000 μm, or from 50 to 500 μm, or from 100 to 300 μm, for example. Positive electrode active material layer 12 includes a positive electrode active material. Positive electrode active material layer 12 may further include a conductive material, a binder, and the like, for example.
The conductive material may form an electron conduction path inside the positive electrode active material layer 12. The amount of the conductive material to be used may be, for example, from 0.1 to 10 parts by mass relative to 100 parts by mass of the positive electrode active material. The conductive material may include any component. The conductive material may include, for example, at least one selected from the group consisting of graphite, acetylene black (AB), Ketjenblack (registered trademark), vapor grown carbon fiber (VGCF), carbon nanotube (CNT), and graphene flake (GF).
The binder is capable of fixing positive electrode active material layer 12 to positive electrode base material 11. The amount of the binder to be used may be, for example, from 0.1 to 10 parts by mass relative to 100 parts by mass of the positive electrode active material. The binder may include any component. The binder may include, for example, at least one selected from the group consisting of PVDF, PVDF-HFP, PTFE, CMC, PAA, PVA, PVP, polyoxyethylene alkyl ether, and derivatives of these.
Positive electrode active material layer 12 may further include an inorganic filler, an organic filler, a solid electrolyte, a surface modifier, a lubricant, a flame retardant, a protective agent, a flux, a coupling agent, an adsorbent, and/or the like, for example. Positive electrode active material layer 12 may include polyoxyethylene allylphenyl ether phosphate, zeolite, a silane coupling agent, MoS2, WO3, and/or the like, for example.
The positive electrode active material may be in particle form, for example. The positive electrode active material may include any component. The positive electrode active material may include a transition metal oxide, a polyanion compound, and/or the like, for example. In a single particle (positive electrode active material), the composition may be uniform, or may be non-uniform. For example, there may be a gradient in the composition from the surface of the particle toward the center. The composition may change contiguously, or may change non-contiguously (in steps).
The transition metal oxide may have any crystal structure. For example, the transition metal oxide may include a crystal structure that belongs to a space group R-3m and/or the like. For example, a compound represented by the general formula “LiMO2” may have a crystal structure that belongs to a space group R-3m. The transition metal oxide may be represented by the following formula (2-1), for example.
In the above formula (2-1), M may include, for example, at least one selected from the group consisting of Co, Mn, and Al. For example, the relationships of −0.5≤a≤0.5, 0<x≤1 may be satisfied.
For example, the relationship of −0.4≤a≤0.4, −0.3≤a≤0.3, −0.2≤a≤0.2, or −0.1≤a≤0.1 may be satisfied.
For example, the relationship of 0<x≤0.1, 0.1≤x≤0.2, 0.2≤x≤0.3, 0.3≤x≤0.4, 0.4≤x≤0.5, 0.5≤x≤0.6, 0.6≤x≤0.7, 0.7≤x≤0.8, 0.8≤x≤0.9, or 0.9≤x≤1 may be satisfied.
The transition metal oxide may include, for example, at least one selected from the group consisting of LiCoO2, LiMnO2, LiNi0.9Co0.1O2, LiNi0.9Mn0.1O2, and LiNiO2.
The transition metal oxide may be represented by the following formula (2-2), for example. A compound represented by the following formula (2-2) may also be called “NCM”.
In the above formula (2-2), the relationships of −0.5≤a≤0.5, 0<x<1, 0<y<1, 0<z<1, x+y+z=1 may be satisfied, for example.
For example, the relationship of 0<x≤0.1, 0.1≤x≤0.2, 0.2≤x≤0.3, 0.3≤x≤0.4, 0.4≤x≤0.5, 0.5≤x≤0.6, 0.6≤x≤0.7, 0.7≤x≤0.8, 0.8≤x≤0.9, or 0.9≤x<1 may be satisfied.
For example, the relationship of 0<y≤0.1, 0.1≤y≤0.2, 0.2≤y≤0.3, 0.3≤y≤0.4, 0.4≤y≤0.5, 0.5≤y≤0.6, 0.6≤y≤0.7, 0.7≤y≤0.8, 0.8≤y≤0.9, or 0.9≤y<1 may be satisfied.
For example, the relationship of 0<z≤0.1, 0.1≤z≤0.2, 0.2≤z≤0.3, 0.3≤z≤0.4, 0.4≤z≤0.5, 0.5≤z≤0.6, 0.6≤z≤0.7, 0.7≤z≤0.8, 0.8≤z≤0.9, or 0.9≤z<1 may be satisfied.
NCM may include, for example, at least one selected from the group consisting of LiNi1/3Co1/3Mn1/3O2, LiNi0.4Co0.3Mn0.3O2, LiNi0.3Co0.4Mn0.3O2, LiNi0.3Co0.3Mn0.4O2, LiNi0.5Co0.2Mn0.3O2, LiNi0.5Co0.3Mn0.2O2, LiNi0.5Co0.4Mn0.1O2, LiNi0.5Co0.1Mn0.4O2, LiNi0.6Co0.2Mn0.2O2, LiNi0.6Co0.3Mn0.1O2, LiNi0.6Co0.1Mn0.3O2, LiNi0.7Co0.1Mn0.2O2, LiNi0.7Co0.2Mn0.1O2, LiNi0.8Co0.1Mn0.1O2, and LiNi0.9Co0.05Mn0.05O2.
The transition metal oxide may be represented by the following formula (2-3), for example. A compound represented by the following formula (2-3) may also be called “NCA”.
In the above formula (2-3), the relationships of −0.5≤a≤0.5, 0<x<1, 0<y<1, 0<<1, x+y+z=1 may be satisfied, for example.
For example, the relationship of 0<x≤0.1, 0.1≤x≤0.2, 0.2≤x≤0.3, 0.3≤x≤0.4, 0.4≤x≤0.5, 0.5≤x≤0.6, 0.6≤x≤0.7, 0.7≤x≤0.8, 0.8≤x≤0.9, or 0.9≤x<1 may be satisfied.
For example, the relationship of 0<y≤0.1, 0.1≤y≤0.2, 0.2≤y≤0.3, 0.3≤y≤0.4, 0.4≤y≤0.5, 0.5≤y≤0.6, 0.6≤y≤0.7, 0.7≤y≤0.8, 0.8≤y≤0.9, or 0.9≤y<1 may be satisfied. For example, the relationship of 0<z≤0.1, 0.1≤z≤0.2, 0.2≤z≤0.3, 0.3≤z≤0.4, 0.4≤z≤0.5, 0.5≤z≤0.6, 0.6≤z≤0.7, 0.7≤z≤0.8, 0.8≤z≤0.9, or 0.9≤z<1 may be satisfied.
NCA may include, for example, at least one selected from the group consisting of LiNi0.7Co0.1Al0.2O2, LiNi0.7Co0.2Al0.1O2, LiNi0.&Co0.1Al0.1O2, LiNi0.8Co0.17Al0.03O2, LiNi0.8Co0.15Al0.05O2, and LiNi0.9Co0.05Al0.05O2.
The positive electrode active material may include two or more NCMs and/or the like, for example. The positive electrode active material may include NCM (0.6≤x) and NCM (x<0.6), for example. “NCM (0.6≤x)” refers to a compound in which x (Ni ratio) in the above formula (2-2) is 0.6 or more. NCM (0.6≤x) may also be called “a high-nickel material”, for example. NCM (0.6≤x) includes LiNi0.8Co0.1Mn0.1O2 and/or the like, for example. “NCM(x<0.6)” refers to a compound in which x (Ni ratio) in the above formula (2-2) is less than 0.6. NCM (x<0.6) includes LiNi1/3Co1/3Mn1/3O2 and/or the like, for example. The mixing ratio (mass ratio) between NCM (0.6≤x) and NCM (x<0.6) may be “NCM (0.6≤x)/NCM (x<0.6)=9/1 to 1/9”, or “NCM (0.6≤x)/NCM (x<0.6)=9/1 to 4/6”, or “NCM (0.6≤x)/NCM (x<0.6)=9/1 to 3/7”, for example.
The positive electrode active material may include NCA and NCM, for example. The mixing ratio (mass ratio) between NCA and NCM may be “NCA/NCM=9/1 to 1/9”, “NCA/NCM=9/1 to 4/6”, or “NCA/NCM=9/1 to 3/7”, for example. Between NCA and NCM, the Ni ratio may be the same or may be different. The Ni ratio of NCA may be more than the Ni ratio of NCM. The Ni ratio of NCA may be less than the Ni ratio of NCM.
The transition metal oxide may include a crystal structure that belongs to a space group C2/m and/or the like, for example. The transition metal oxide may be represented by the following formula (2-4), for example.
In the above formula (2-4), M may include, for example, at least one selected from the group consisting of Ni, Co, Mn, and Fe.
The positive electrode active material may include a mixture of LiMO2 (space group R-3m) and Li2MO3 (space group C2/m), for example. The positive electrode active material may include a solid solution that is formed of LiMO2 and Li2MO3 (Li2MO3-LiMO2), and/or the like, for example.
The transition metal oxide may include a crystal structure that belongs to a space group Fd-3m, and/or the like, for example. The transition metal oxide may be represented by, for example, the following formula (2-5):
In the above formula (2-5), M may include, for example, at least one selected from the group consisting of Ni, Fe, and Zn. For example, the relationship of 0≤x≤2 may be satisfied.
LiM2O4 (space group Fd-3m) may include, for example, at least one selected from the group consisting of LiMn2O4 and LiMn1.5Ni0.5O4. The positive electrode active material may include a mixture of LiMO2 (space group R-3m) and LiM2O4 (space group Fd-3m), for example. The mixing ratio (mass ratio) between LiMO2 (space group R-3m) and LiM2O4 (space group Fd-3m) may be “LiMO2/LiM2O4=9/1 to 9/1”, “LiMO2/LiM2O4=9/1 to 5/5”, or “LiMO2/LiM2O4=9/1 to 7/3”, for example.
The polyanion compound may include a phosphoric acid salt (such as LiFePO4 for example), a silicic acid salt, a boric acid salt, and/or the like, for example. The polyanion compound may be represented by the following formulae (2-6) to (2-9), for example.
In the above formulae (2-6) to (2-9), M may include, for example, at least one selected from the group consisting of Fe, Mn, Co. In the above formula (2-7), the relationship of 0≤x≤2 may be satisfied, for example.
The positive electrode active material may include a mixture of LiMO2 (space group R-3m) and the polyanion compound, for example. The mixing ratio (mass ratio) between LiMO2 (space group R-3m) and the polyanion compound may be “LiMO2/(polyanion compound)=9/1 to 9/1”, “LiMO2/(polyanion compound)=9/1 to 5/5”, or “LiMO2/(polyanion compound)=9/1 to 7/3”, for example.
To the positive electrode active material, a dopant may be added. The dopant may be diffused throughout the entire particle, or may be locally distributed. For example, the dopant may be locally distributed on the particle surface. The dopant may be a substituted solid solution atom, or may be an intruding solid solution atom. The amount of the dopant to be added (the molar fraction relative to the total amount of the positive electrode active material) may be from 0.01 to 5%, or may be from 0.1 to 3%, or may be from 0.1 to 1%, for example. A single type of dopant may be added, or two or more types of dopant may be added. The two or more dopants may form a complex.
The dopant may include, for example, at least one selected from the group consisting of B, C, N, a halogen, Si, Na, Mg, Al, Mn, Co, Cr, Sc, Ti, V, Cu, Zn, Ga, Ge, Se, Sr, Y, Zr, Nb, Mo, In, Pb, Bi, Sb, Sn, W, La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, and an actinoid.
For example, to NCA, a combination of “Zr, Mg, W, Sm”, a combination of “Ti, Mn, Nb, Si, Mo”, or a combination of “Er, Mg” may be added. For example, to NCM, Ti may be added. For example, to NCM, a combination of “Zr, W”, a combination of “Si, W”, or a combination of “Zr, W, Al, Ti, Co” may be added.
Positive electrode 10 may include a composite particle. The composite particle includes a core particle and a shell layer. The core particle includes a positive electrode active material. The shell layer covers at least part of the surface of the core particle. The shell layer may have a thickness from 1 to 3000 nm, or from 5 to 2000 nm, or from 10 to 1000 nm, or from 10 to 100 nm, or from 10 to 50 nm, for example. The thickness of the shell layer may be measured in an SEM image of a cross section of the particle, and/or the like, for example. More specifically, the composite particle is embedded in a resin material to prepare a sample. With the use of an ion milling apparatus, a cross section of the sample is exposed. For example, an ion milling apparatus with the trade name “ArBlade (registered trademark) 5000” manufactured by Hitachi High-Technologies (or a similar product) may be used. The cross section of the sample is examined by an SEM. For example, an SEM apparatus with the trade name “SU8030” manufactured by Hitachi High-Technologies (or a similar product) may be used. For each of ten composite particles, the thickness of the shell layer is measured in twenty fields of view. The arithmetic mean of a total of 200 thickness measurements is used.
The ratio of the part of the surface of the core particle covered by the shell layer is also called “a covering rate”. The covering rate may be 1% or more, or 10% or more, or 30% or more, or 50% or more, or 70% or more, for example. The covering rate may be 100% or less, or 90% or less, or 80% or less, for example.
For example, the covering rate may be measured by XPS (X-ray Photoelectron Spectroscopy). For example, an XPS apparatus with the trade name “PHI X-tool” manufactured by ULVAC-PHI (or a similar product) may be used. A sample (powder) is loaded in the XPS apparatus. Narrow scan analysis is carried out. The measurement data is processed with an analysis software. For example, an analysis software with the trade name “MulTiPak” manufactured by ULVAC-PHI (or a similar product) may be used. The measurement data is analyzed to detect a plurality of types of elements. From the area of each peak, the ratio of the detected element is determined. By the following equation (2-10), the covering rate is determined.
For example, when the core particle includes NCM, I0 represents the total ratio of the elements “Ni, Co, Mn”. For example, when the core particle includes NCA, I0 represents the total ratio of the elements “Ni, Co, Al”. For example, when the shell layer includes P and B, I1 represents the total ratio of the elements “P, B”.
The shell layer may include any component. The shell layer may include an elementary substance, organic matter, an inorganic acid salt, an organic acid salt, a hydroxide, an oxide, a carbide, a nitride, a sulfide, a halide, and/or the like, for example. The shell layer may include, for example, at least one selected from the group consisting of B, Al, W, Zr, Ti, Co, F, lithium compound (such as Li2CO3, LiHCO3, LiOH, Li2O, for example), tungsten oxide (such as WO3, for example), titanium oxide (such as TiO2, for example), zirconium oxide (such as ZrO2, for example), boron oxide, boron phosphate (such as BPO4, for example), aluminum oxide (such as Al2O3, for example), boehmite, aluminum hydroxide, phosphoric acid salt [such as Li3PO4, (NH4)3PO4, AIPO4, for example], boric acid salt (such as Li2B4O7, LiBO3, for example), polyacrylic acid salt (such as Li salt, Na salt, NH4 salt), acetic acid salt (such as Li salt, for example), CMC (such as Na salt, Li salt, NH4 salt), LiNbO3, LizTiO3, and Li-containing halide (such as LiAlCl4, LiTiAlF6, LiYBr6, LiYCl6, for example).
Each of “a hollow particle” and “a solid particle” is a secondary particle (an aggregate of primary particles). In a cross-sectional image of “a hollow particle”, the proportion of the area of the central cavity relative to the entire cross-sectional area of the particle is 30% or more. The proportion of the cavity in the hollow particle may be 40% or more, or 50% or more, or 60% or more, for example. In a cross-sectional image of “a solid particle”, the proportion of the area of the central cavity relative to the entire cross-sectional area of the particle is less than 30%. The proportion of the cavity in the solid particle may be 20% or less, or 10% or less, or 5% or less, for example. The positive electrode active material may be hollow particles, or may be solid particles. A mixture of hollow particles and solid particles may be used. The mixing ratio (mass ratio) between hollow particles and solid particles may be “(hollow particles)/(solid particles)=1/9 to 9/1”, or “(hollow particles)/(solid particles)=2/8 to 8/2”, or “(hollow particles)/(solid particles)=3/7 to 7/3”, or “(hollow particles)/(solid particles)=4/6 to 6/4”, for example.
The positive electrode active material may have a unimodal particle size distribution (based on the number), for example. The positive electrode active material may have a multimodal particle size distribution, for example. The positive electrode active material may have a bimodal particle size distribution, for example. That is, the positive electrode active material may include “large particles” and “small particles”. When the particle size distribution is bimodal, the particle size corresponding to the peak top of the larger particle size is regarded as the particle size of the large particles (dL). The particle size corresponding to the peak top of the smaller particle size is regarded as the particle size of the small particles (dS). The particle size ratio (dL/dS) may be from 2 to 10, or from 2 to 5, or from 2 to 4, for example. dL may be from 8 to 20 μm, or from 8 to 15 μm, for example. dS may be from 1 to 10 μm, or from 1 to 5 μm, for example.
For example, with the use of a waveform analysis software, peak separating processing may be carried out for the particle size distribution. The ratio between the peak area of the large particles (SL) and the peak area of the small particles (SS) may be “SL/SS=1/9 to 9/1”, or “SL/SS=5/5 to 9/1”, or “SL/SS=7/3 to 9/1”, for example.
The number-based particle size distribution is measured by a microscope method. From positive electrode active material layer 12, a plurality of cross-sectional samples are taken. The cross-sectional sample may include a cross section vertical to the surface of positive electrode active material layer 12, for example. By ion milling and/or the like, for example, cleaning is carried out to the side that is to be observed. By SEM, the cross-sectional sample is examined. The magnification for the examination is adjusted in such a way that 10 to 100 particles are contained within the examination field of view. The Feret diameters of all the particles in the image are measured. “Feret diameter” refers to the distance between two points located farthest apart from each other on the outline of the particle. The plurality of the cross-sectional samples are examined to obtain a total of 1000 or more Feret diameters. From the 1000 or more Feret diameters, number-based particle size distribution is created.
The bimodal particle size distribution may be formed by two types of particles mixed together. These two types of particles have different particle size distributions.
For example, the two types of particles may have different D50. For example, the large particles may have a D50 from 8 to 20 μm, or from 8 to 15 μm. For example, the small particles may have a D50 from 1 to 10 μm, or from 1 to 5 μm. The ratio of the D50 of the large particles to the D50 of the small particles may be from 2 to 10, or from 2 to 5, or from 2 to 4, for example. The mixing ratio (mass ratio) between the large particles and the small particles may be “(large particles)/(small particles)=1/9 to 9/1”, or “(large particles)/(small particles)=5/5 to 9/1”, or “(large particles)/(small particles)=7/3 to 9/1”, for example.
The large particles and the small particles may have the same composition, or may have different compositions. For example, the large particles may be NCA and the small particles may be NCM. For example, the large particles may be NCM (0.6≤x) and the small particles may be NCM (x<0.6).
The electrolyte solution is a liquid electrolyte. The electrolyte solution includes Li ions. The electrolyte solution may include a solute and a solvent, for example.
The concentration of the solute may be from 0.5 to 1 mol/L, or from 1 to 1.5 mol/L, or from 1.5 to 2 mol/L, or from 2 to 2.5 mol/L, or from 2.5 to 3 mol/L, for example. The solute includes a supporting salt (a Li salt). The solute may include an inorganic acid salt, an imide salt, an oxalato complex, a halide, and/or the like, for example. The solute may include, for example, at least one selected from the group consisting of LiPF6, LiBF4, LiCIO4, LiAsF6, LiSbF6, LIN(SO2F)2 which has the common name “LiFSI”, LIN(SO2CF3)2 which has the common name “LiTFSI”, LiB(C2O4)2 which has the common name “LiBOB”, LiBF2(C2O4) which has the common name “LiDFOB”, LiPF2(C2O4)2 which has the common name “LiDFOP”, LiPO2F2, FSO3Li, LiI, LiBr, and derivatives of these.
The electrolyte solution may include an ether-based solvent, for example. The solvent may include, for example, at least one selected from the group consisting of tetrahydrofuran (THF), 1,4-dioxane (DOX), 1,3-dioxolane (DOL), 1,2-dimethoxyethane (DME), 1,2-diethoxyethane (DEE), ethylglyme, triglyme, tetraglyme, hydrofluoroether (HFE), and derivatives of these.
HFE may include, for example, at least one selected from the group consisting of a difluoromethyl group, a 2,2-difluoroethyl group, a 2,2,2-trifluoroethyl group, a 1,1,2,2-tetrafluoroethyl group, a 2,2,3,3,3-pentafluoropropyl group, a 2,2,3,3-tetrafluoropropyl group, a 1,1,1,3,3,3-hexafluoroisopropyl group, a 1,1,2,3,3,3-hexafluoropropyl group, a 2,2,3,3,4,4,4-heptafluorobutyl group, a 2,2,3,3,4,4-hexafluorobutyl group, and a 2,2,3,3,4,4,5,5-octafluoropentyl group.
HFE may include, for example, at least one selected from the group consisting of 1,1,2,2-tetrafluoroethyl 2,2,3,3-tetrafluoropropyl ether, 2,2,2-trifluoroethyl ether, difluoromethyl 2,2,3,3-tetrafluoropropyl ether, 2,2,3,3-tetrafluoropropyl 1,1,2,3,3,3-hexafluoropropyl ether, 2,2,3,3,4,4,5,5-octafluoropentyl 1,1,2,2-tetrafluoroethyl ether, and derivatives of these.
The electrolyte solution may include a carbonate-based solvent (a carbonate-ester-based solvent), for example. The solvent may include a cyclic carbonate, a chain carbonate, a fluorinated carbonate, and/or the like, for example. The solvent may include, for example, at least one selected from the group consisting of ethylene carbonate (EC), propylene carbonate (PC), butylene carbonate (BC), dimethyl carbonate (DMC), diethyl carbonate (DEC), ethyl methyl carbonate (EMC), monofluoroethylene carbonate (FEC), difluoroethylene carbonate, 4,4-difluoroethylene carbonate, trifluoroethylene carbonate, perfluoroethylene carbonate, fluoropropylene carbonate, difluoropropylene carbonate, and derivatives of these.
The solvent may include a cyclic carbonate (such as EC, PC, FEC) and a chain carbonate (such as EMC, DMC, DEC). The mixing ratio between the cyclic carbonate and the chain carbonate (volume ratio) may be “(cyclic carbonate)/(chain carbonate)=1/9 to 4/6”, or “(cyclic carbonate)/(chain carbonate)=2/8 to 3/7”, or “(cyclic carbonate)/(chain carbonate)=3/7 to 4/6”, for example.
The solvent may include a cyclic carbonate (such as EC, PC) and a fluorinated cyclic carbonate (such as FEC). The mixing ratio between the cyclic carbonate and the fluorinated cyclic carbonate (volume ratio) may be “(cyclic carbonate)/(fluorinated cyclic carbonate)=99/1 to 90/10”, or “(cyclic carbonate)/(fluorinated cyclic carbonate)=9/1 to 1/9”, or “(cyclic carbonate)/(fluorinated cyclic carbonate)=9/1 to 7/3”, or “(cyclic carbonate)/(fluorinated cyclic carbonate)=3/7 to 1/9”, for example.
The solvent may include EC, FEC, EMC, DMC, and DEC, for example. The volume ratio of these components may satisfy the relationship represented by the following equation (3-1), for example.
In the above equation (3-1), VEC, VFEC, VEMC, VDMC, and VDEC represent the volume ratios of EC, FEC, EMC, DMC, and DEC, respectively.
For example, the relationships of 1≤VEC≤4, 0≤VFEC≤3, VEC+VFEC≤4, 0≤VEMC≤9, 0≤VDMC≤9, 0≤VDEC≤9, and 6≤VEMC+VDMC+VDEC≤9 may be satisfied.
In the above equation (3-1),
The solvent may have a composition of “EC/EMC-3/7”, “EC/DMC=3/7”, “EC/FEC/DEC=1/2/7”, “EC/DMC/EMC=3/4/3”, “EC/DMC/EMC=3/3/4”, “EC/FEC/DMC/EMC=2/1/4/3”, “EC/FEC/DMC/EMC=1/2/4/3”, “EC/FEC/DMC/EMC=2/1/3/4”, “EC/FEC/DMC/EMC=1/2/3/4” (volume ratio), and/or the like, for example.
The electrolyte solution may include any additive. The amount to be added (the mass fraction to the total amount of the electrolyte solution) may be from 0.01 to 5%, or from 0.05 to 3%, or from 0.1 to 1%, for example. The additive may include an SEI (Solid Electrolyte Interphase) formation promoter, an SEI formation inhibitor, a gas generation agent, an overcharging inhibitor, a flame retardant, an antioxidant, an electrode-protecting agent, a surfactant, and/or the like, for example.
The additive may include, for example, at least one selected from the group consisting of vinylene carbonate (VC), vinylethylene carbonate (VEC), 1,3-propane sultone (PS), tert-amylbenzene, 1,4-di-tert-butylbenzene, biphenyl (BP), cyclohexylbenzene (CHB), ethylene sulfite (ES), propane sultone (PS), ethylene sulfate (DTD), γ-butyrolactone, phosphazene compound, carboxylate ester [such as methyl formate (MF), methyl acetate (MA), methyl propionate (MP), diethyl malonate (DEM), for example], fluorobenzene (such as monofluorobenzene (FB), 1,2-difluorobenzene, 1,3-difluorobenzene, 1,4-difluorobenzene, 1,2,3-trifluorobenzene, 1,2,4-trifluorobenzene, 1,3,5-trifluorobenzene, 1,2,3,4-tetrafluorobenzene, 1,2,3,5-tetrafluorobenzene, 1,2,4,5-tetrafluorobenzene, pentafluorobenzene, hexafluorobenzene, for example), fluorotoluene (such as 2-fluorotoluene, 3-fluorotoluene, 4-fluorotoluene, 2,3-difluorotoluene, 2,4-difluorotoluene, 2,5-difluorotoluene, 2,6-difluorotoluene, 3,4-difluorotoluene, octafluorotoluene, for example), benzotrifluoride (such as benzotrifluoride, 2-fluorobenzotrifluoride, 3-fluorobenzotrifluoride, 4-fluorobenzotrifluoride, 2-methylbenzotrifluoride, 3-methylbenzotrifluoride, 4-methylbenzotrifluoride, for example), fluoroxylene (such as 3-fluoro-o-xylene, 4-fluoro-o-xylene, 2-fluoro-m-xylene, 5-fluoro-m-xylene, for example), sulfur-containing heterocyclic compound (such as benzothiazole, 2-methylbenzothiazole, tetrathiafulvalene, for example), nitrile compound (such as adiponitrile, succinonitrile, for example), phosphate (such as trimethyl phosphate, triethyl phosphate, for example), carboxylic anhydride (such as acetic anhydride, propionic anhydride, oxalic anhydride, succinic anhydride, maleic anhydride, phthalic anhydride, benzoic anhydride, for example), alcohol (such as methanol, ethanol, n-propyl alcohol, ethylene glycol, diethylene glycol monomethyl ether, for example), and derivatives of these.
The components described above as the solute and the solvent may be used as the additive (a trace component). The additive may include, for example, at least one selected from the group consisting of LiBF4, LiFSI, LiTFSI, LiBOB, LIDFOB, LiDFOP, LiPO2F2, FSO3Li, LiI, LiBr, HFE, DOX, PC, FEC, and derivatives of these.
The electrolyte solution may include an ionic liquid. The electrolyte solution may include, for example, at least one selected from the group consisting of a sulfonium salt, an ammonium salt, a pyridinium salt, a piperidinium salt, a pyrrolidinium salt, a morpholinium salt, a phosphonium salt, an imidazolium salt, and derivatives of these.
Battery 100 may include a gelled electrolyte. The gelled electrolyte includes an electrolyte solution and a polymer material. The polymer material may form a polymer matrix. The polymer material may include, for example, at least one selected from the group consisting of PVdF, PVdF-HFP, PAN, PVdF-PAN, polyethylene oxide (PEO), polyethylene glycol (PEG), and derivatives of these.
Separator 30 is electrically insulating. Separator 30 may include, for example, at least one selected from the group consisting of a resin film, an inorganic particle layer, and an organic particle layer. Separator 30 may include a resin film and an inorganic particle layer, for example.
The resin film is porous. The resin film may include a microporous film, a nonwoven fabric, and/or the like, for example. The resin film includes a resin skeleton. The resin skeleton may be contiguous in mesh form, for example. Gaps in the resin skeleton form pores. The resin film allows the electrolyte solution to permeate therethrough. The resin film may have an average pore size of 1 μm or less, for example. The resin film may have an average pore size from 0.01 to 1 μm, or from 0.1 to 0.5 μm, for example. “Average pore size” may be measured by mercury porosimetry. The resin film may have a Gurley value from 50 to 250 s/100 cm3, for example. “Gurley value” may be measured by a Gurley test method.
The resin film may include, for example, at least one selected from the group consisting of an olefin-based resin, a urethane-based resin, a polyamide-based resin, a cellulose-based resin, a polyether-based resin, an acrylic-based resin, a polyester-based resin, and the like. The resin film may include, for example, at least one selected from the group consisting of polyethylene (PE), polypropylene (PP), polyamide (PA), polyamide-imide (PAI), polyimide (PI), aromatic polyamide (aramid), and polyphenylene ether (PPE), and derivatives of these. The resin film may be formed by stretching, phase separation, and/or the like, for example. The resin film may have a thickness from 5 to 50 μm, or from 10 to 25 μm, for example.
The resin film may have a monolayer structure. The resin film may consist of a PE layer, for example. A skeleton of a PE layer is formed of PE. The PE layer may have shut-down function. The resin film may have a multilayer structure, for example. The resin film may include a PP layer and a PE layer, for example. A skeleton of a PP layer is formed of PP. The resin film may have a three-layer structure, for example. The resin film may be formed by stacking a PP layer, a PE layer, and a PP layer in this order, for example. The thickness of the PE layer may be from 5 to 20 μm, for example. The thickness of the PP layer may be from 3 to 10 μm, for example.
The inorganic particle layer may be formed on the surface of the resin film. The inorganic particle layer may be formed on only one side of the resin film, or may be formed on both sides of the resin film. The inorganic particle layer may be formed on the side facing positive electrode 10, or may be formed on the side facing negative electrode 20.
The inorganic particle layer is porous. The inorganic particle layer includes inorganic particles. The inorganic particles may also be called “an inorganic filler”. Gaps between the inorganic particles form pores. The inorganic particle layer may have a thickness from 0.5 to 10 μm, or from 1 to 5 μm, for example. The inorganic particles may include a heat-resistant material, for example. The inorganic particle layer that includes a heat-resistant material is also called “HRL (Heat Resistance Layer)”. The inorganic particles may include at least one selected from the group consisting of boehmite, alumina, zirconia, titania, magnesia, silica, and the like. The inorganic particles may have any shape. The inorganic particles may be spherical, rod-like, plate-like, fibrous, and/or the like, for example. The inorganic particles may have a D50 from 0.1 to 10 μm, or from 0.5 to 3 μm, for example. The inorganic particle layer may further include a binder. The binder may include, for example, at least one selected from the group consisting of an acrylic-based resin, a polyamide-based resin, a fluorine-based resin, an aromatic-polyether-based resin, and a liquid-crystal-polyester-based resin, and the like.
Separator 30 may include an organic particle layer, for example. Separator 30 may include an organic particle layer instead of the resin film, for example. Separator 30 may include an organic particle layer instead of the inorganic particle layer, for example. Separator 30 may include both the resin film and an organic particle layer. Separator 30 may include both the inorganic particle layer and an organic particle layer. Separator 30 may include the resin film, the inorganic particle layer, and an organic particle layer.
The organic particle layer may have a thickness from 0.1 to 50 μm, or from 0.5 to 20 μm, or from 0.5 to 10 μm, or from 1 to 5 μm, for example. The organic particle layer includes organic particles. The organic particles may also be called “an organic filler”. The organic particles may include a heat-resistant material. The organic particles may include, for example, at least one selected from the group consisting of PE, PP, PTFE, PI, PAI, PA, aramid, and the like. The organic particles may be spherical, rod-like, plate-like, fibrous, and/or the like, for example. The organic particles may have a D50 from 0.1 to 10 μm, or from 0.5 to 3 μm, for example.
Separator 30 may include a mixed layer, for example. The mixed layer includes both inorganic particles and organic particles.
In the present embodiment, as long as dispersed phase 22b (a Li-ion conductor) is positioned within Li metal layer 22 and a Li metal dissolution/deposition reaction takes place at negative electrode 20, the other configurations (such as the combination of the positive electrode, the separator, and the electrolyte solution, and the like) are not particularly limited. For example, certain elements may be extracted from the first configuration example, the second configuration example, and the third configuration example, and they may be combined together in a freely-selected manner.
Test batteries (anode-free batteries) according to Nos. 1 to 55 were produced in the procedure described below. For example, hereinafter, “the test battery according to No. 1” may be simply referred to as “No. 1” and the like.
As a positive electrode base material, an Al foil was prepared. A positive electrode coating material was applied to the surface of the Al foil with the use of a die coater, and dried. By this, a positive electrode active material layer was formed.
With a rolling mill, the resulting positive electrode active material layer was compressed. Thus, a positive electrode raw sheet was produced. The resulting positive electrode raw sheet was cut into a predetermined shape, and thereby a positive electrode was prepared. The positive electrode active material was LiNi1/3Co1/3Mn1/3O2.
As a separator, a resin film (thickness, 20 μm) was prepared. The resin film included an olefin-based resin.
As a negative electrode base material, a Cu foil was prepared. The Cu foil was cut into a predetermined shape, and thereby a negative electrode was prepared.
The positive electrode, the separator, and the negative electrode were stacked in this order, and thereby a power generation element was formed. The resulting power generation element was placed inside an exterior package. Into the exterior package, an electrolyte solution was injected. The composition of the electrolyte solution was as described below.
After the electrolyte solution was injected, the exterior package was hermetically sealed. Thus, a test battery was assembled. The resulting test battery was charged in a constant-current mode, and thereby a Li metal layer was formed on the surface of the negative electrode base material. In this manner, a test battery was produced.
Commercially available Li3PO4 powder (Li-ion conductivity, 1×10−7 S/cm) was pulverized with the use of a mechanochemical apparatus. The pulverized product was sintered at a low temperature. Pulverization and low-temperature sintering were repeated alternately. In this manner, the Li-ion conductivity of Li3PO4 was adjusted to 2×10−9 S/cm.
A PVDF solution was prepared. The Li3PO4 powder (Li-ion conductivity, 2×10−9 S/cm) and the PVDF solution were mixed to prepare a coating material. The mixing ratio was “(Li-ion conductor)/(PVDF solution)=80/20 (mass ratio)”. The coating material was applied to the surface of the negative electrode base material by gravure coating, and dried. By this, a negative electrode was prepared. Except for these, in the same manner as in No. 1, a test battery was assembled. The resulting test battery was charged in a constant-current mode, and thereby a Li metal layer was formed on the surface of the negative electrode base material. In this manner, a test battery was produced.
Li3PO4 powder (Li-ion conductivity, 1×10−7 S/cm) and a PVDF solution were mixed to prepare a coating material. The mixing ratio was “(Li-ion conductor)/(PVDF solution)=99/1 (mass ratio)”. The coating material was applied to the surface of the negative electrode base material by gravure coating, and dried. By this, a negative electrode was prepared. Except for these, in the same manner as in No. 1, a test battery was assembled. The resulting test battery was charged in a constant-current mode, and thereby a Li metal layer was formed on the surface of the negative electrode base material. In this manner, a test battery was produced.
Li3PO4 powder (Li-ion conductivity, 2×10−9 S/cm) and a PVDF solution were mixed to prepare a coating material. Except for this, in the same manner as in No. 3, a test battery was produced.
The OCV (Open Circuit Voltage) of the test battery was adjusted to 3.7 V. In an environment at a temperature of −10° C., at a current of 5 C, the battery was discharged for 8 seconds. By the following equation (5-1), battery resistance was determined.
Battery resistance is shown in Table 1 to Table 4 (
The discharged capacity at the 200th cycle was divided by the discharged capacity at the first cycle to determine cycle capacity retention. The cycle capacity retention is expressed in percentage. The cycle capacity retention is shown in Table 1 to Table 4 (
The test battery was disassembled at an SOC of 100%, and the negative electrode was collected. In a cross section of the Li metal layer, distribution of the Li-ion conductor was checked. Further, the presence ratio of the Li-ion conductor was measured in the procedure described above.
No. 3 and No. 2 are different in the volume fraction of the binder. In No. 3, the Li-ion conductor was distributed inside the Li metal layer (see
No. 4 and No. 3 are different in the Li-ion conductivity of the Li-ion conductor. In No. 4, the Li-ion conductor was distributed inside the Li metal layer. Cycle endurance of No. 4 was markedly improved as compared to No. 3.
When the Li-ion conductivity of the Li-ion conductor having various compositions is from 1.0×10−13 to 2.0×10−9 S/cm, cycle endurance tends to be improved (see
| Number | Date | Country | Kind |
|---|---|---|---|
| 2023-021504 | Feb 2023 | JP | national |
