WO2020175506A1 - 活物質、それを用いた正極合剤及び固体電池 - Google Patents
活物質、それを用いた正極合剤及び固体電池 Download PDFInfo
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- WO2020175506A1 WO2020175506A1 PCT/JP2020/007578 JP2020007578W WO2020175506A1 WO 2020175506 A1 WO2020175506 A1 WO 2020175506A1 JP 2020007578 W JP2020007578 W JP 2020007578W WO 2020175506 A1 WO2020175506 A1 WO 2020175506A1
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- C01G53/50—Nickelates containing alkali metals, e.g. LiNiO2 containing manganese of the type [MnO2]n-, e.g. Li(NixMn1-x)O2, Li(MyNixMn1-x-y)O2
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- H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
- H01M4/50—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese
- H01M4/505—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
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- H01M4/52—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
- H01M4/525—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
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- C01P2004/82—Particles consisting of a mixture of two or more inorganic phases two phases having the same anion, e.g. both oxidic phases
- C01P2004/84—Particles consisting of a mixture of two or more inorganic phases two phases having the same anion, e.g. both oxidic phases one phase coated with the other
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- H01M4/131—Electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx
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- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
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- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Definitions
- the present invention relates to an active material used for a solid state battery.
- Solid electrolytes used for solid-state batteries are required to have as high ionic conductivity as possible and be chemically and electrochemically stable.
- lithium halide, lithium nitride, lithium salt or their derivatives are known as candidate materials for the solid electrolyte.
- a sulfide solid electrolyte has been studied as one of solid electrolytes used for a solid-state battery.
- the interfacial resistance between the electrode active material and the sulfide solid electrolyte becomes high, which limits the movement of lithium ions.
- the reason for this is believed to be that the electrode active material and the sulfide solid electrolyte react with each other to form a resistance layer at the interface between the two.
- Patent Documents 1 and 2 attempt to suppress the increase in interfacial resistance by coating the surface of the positive electrode active material with a specific compound.
- Patent Document 1 ⁇ 32009081 554 eight 1
- Patent Document 2 113 201 82 1 9229 8 1
- the present invention provides a lithium battery between a positive electrode active material and a solid electrolyte. ⁇ 0 2020/175 506 2 (: 170? 2020 /007578
- the main purpose of the invention is to provide an active material capable of quickly transferring and receiving muion.
- the present invention relates to an active material used in a solid-state battery,
- At least one peak was observed in the range of 0.145 nm or more and 0.185 n or less, and 0.280 nm or more.
- ⁇ At least one peak is observed in the range of 3 310 n or less,
- Laser diffraction scattering particle size mode diameter of the active material due to volume particle size distribution measurement obtained by measuring the distribution measuring method and the mouth 1 0 (respectively "mode diameter", referred. To as “mouth 1 0") relates to, for mode diameter , Is the percentage of the absolute value of the difference between the mode diameter and ⁇ ! ⁇ ( ⁇ Mode diameter 10 ! ⁇
- Fig. 1 is a radial distribution function obtained by measurement of an X-ray absorption fine structure measured for an oxide containing lithium and niobium.
- FIG. 2 shows whether or not there is a peak in the radial distribution function obtained by measuring the X-ray absorption fine structure measured for the positive electrode active material obtained in Example 3. It is a graph which shows a method.
- FIG. 3 is a radial distribution function obtained by measuring the X-ray absorption fine structure measured for the positive electrode active material obtained in Example 3.
- the present invention relates to an active material used for a solid state battery.
- the active material of the present invention has an X-ray absorption fine structure (hereinafter Also called. ), at least one peak is observed in the range of 0.145 nm or more and 0.185 nm or less, and 0.2. ⁇ 02020/175506 3 ⁇ (: 170? 2020 /007578
- the active material of the present invention has a radial distribution function obtained by the measurement of 8 3 in a range of 0.1 45 nm or more and 0.1 85 n or less. At least one peak is observed. The peak position is specified by the position of the peak apex. The definition of peak will be described later.
- the peak position observed in the present invention may be, for example, 0.18 nm or more, 0.151 or more, or 0.154 or more. On the other hand, the peak position may be, for example, 0.180 n or less.
- the number of peaks observed in the above range may be at least one, and may be only one, or may be two or more.
- the active material of the present invention is: At least one peak is observed in the following range.
- the peak position observed in the present invention may be, for example, ⁇ .285 ⁇ ! or more. On the other hand, the peak position is, for example, ⁇ . It may be the following.
- the active material of the present invention preferably has core particles and a coating layer arranged on the surfaces of the core particles.
- a coating layer composed of an element of lithium (!_ ⁇ ), a metal element of 8 (excluding lithium (!_ ⁇ ) element) and an oxygen element and containing an oxide having a specific chemical structure is used. Is preferred.
- this oxide is referred to as "!_ _80 compound” for convenience.
- the !_ ⁇ compound used in the present invention is characterized by observing a peak at a specific interatomic distance in the radial distribution function obtained by measurement of the active material.
- the metal element eight is niobium
- the vertical axis shows the existence probability of atoms located around niobium.
- the peak observed in the range of 0.145 nm or more and 0.185 n or less corresponds to the distance between the niobium atom and the oxygen atom, and is 0.280 nm or more.
- the active material of the present invention has an interface with the solid electrolyte. It is possible to suppress an increase in resistance and consequently improve battery performance.
- the peak is observed in the radial distribution function, which means that the radial distribution function may include a portion or Shiyoruda _ moiety, such as a convex upward.
- the presence/absence of a peak was determined by differentiating the radial distribution function twice using a 3 I ⁇ 1 ⁇ company. Note that, for example, in Example 3 described later, as shown in FIG. A minimum value is obtained by differentiating the radial distribution function twice for the peaks observed in the following range. From this, it can be said that in Example 3, peaks are observed in the range of 0.145 nm or more and 0.185 n or less.
- the !__80 compound preferably used in the present invention is Has a peak at a specific position of a specific interatomic distance in the radial distribution function obtained from the measurement. In contrast to this, so far known !_
- the compound of the I_8_O system does not have a peak at the predetermined position defined in the present invention in the radial distribution function obtained from Eq.
- !_ ⁇ 1 ⁇ 1 ⁇ ⁇ 3 which is one of the conventionally known !_ ⁇ 1810 series compounds, is ⁇ . 1 4 5 ⁇ !
- Also known in the past! -1 _ ⁇ 3 1 ⁇ 1 13 ⁇ 4 which is another kind of ⁇ 18100 series compounds is 0.28
- XA FS is a method for analyzing an absorption spectrum obtained by irradiating a substance with X-rays. In the absorption spectrum obtained by irradiating a substance with X-rays, a sharp rising edge peculiar to the elements contained in the substance, that is, the absorption edge is observed. The fine structure that appears in the soil near the absorption edge of about 50 eV is called XANES (X-ray Absorption Near Edge Structure).
- the vibrating structure that appears from the absorption edge to the high energy side of about 1000 eV is called EXAFS (Extended X-ray Absorption Fine Structure).
- the area that combines XANES and EXAFS is called XAFS.
- XAFS it is possible to evaluate the local structure (interatomic distance, coordination number) and chemical state (valence, coordination structure) around the element of interest in the sample.
- XAFS is a non-destructive measurement method and is a measurement method capable of obtaining information on the outermost surface of a substance
- the active material itself of the present invention can be used as a measurement target, and the coating layer of the active material Can get information
- the operation is performed, for example, by the procedure described below.
- the amount of the sample and boron nitride is optimized as appropriate according to the concentration of the A element contained in the sample to be measured and the X-ray absorption coefficient of the L i AO compound and the compound forming the core material particles.
- X-ray absorbance (y axis) is calculated by the following formula, and XAFS scan is performed by plotting on X axis _ y axis. I got a vector.
- the P re-edge region (the region from 150 eV to 45 eV below the absorption edge), which is the background absorption, and P ⁇ st
- the XAFS spectrum is standardized by fitting with the _ edge region (a region of about 150 eV or more and 1 300 eV or less from the absorption edge).
- fitting with a spline curve is performed.
- the parameters used for fitting the spline curve in the analysis with the software are as follows.
- the active material of the present invention preferably has core particles and a coating layer arranged on the surfaces of the core particles.
- the coating layer is selected from the group consisting of L i, A element (A is T i, Z r, T a, N b, Z n, W and AI). 1 or 2 or more elements) and ⁇ , that is, the above-mentioned L i AO compound.
- the compound includes, on the surface of the core material particles, a mode of existing as particles, a mode of existing as agglomerated particles formed by agglomeration of particles, and a mode of existing as a layer. “Existing in the form of a layer” means a state in which the Li AO compound exists with a thickness.
- the thickness thereof is preferably 0.5 nm or more and 200 nm or less, of which 0.7 nm or more or 100 nm or less, and 1 nm or more or 90 nm or more thereof. It is preferably not more than nm, more preferably not more than 80 nm, still more preferably not more than 70 nm, still more preferably not more than 60 nm, still more preferably not more than 50 nm. It is preferably not more than 40 nm, and more preferably not more than 40 nm. By setting it in such a range, it can be made to function as a favorable lithium ion conductive layer with a small interface resistance. Layer thickness ⁇ 0 2020/175 506 8 ⁇ (: 170? 2020 /007578
- the surface of the core material particle There may be a part of the surface of the core material particle or a part thereof where the 1_O compound does not exist. Above all, it is preferable that the 1-800 compound covers 30% or more of the entire surface area of the core material particles, of which 40% or more, and more preferably 50% or more.
- the fact that the surface of the core particles is covered with 1_O compound means that, for example, the scanning transmission electron microscope (3 chome 1 ⁇ /1) and the energy dispersive X-ray This can be confirmed by observing the surface of the core material particles by combining analysis (Mr.
- the thickness of the 1-880 compound coating the surface of the core material particles does not have to be uniform.
- the 1_80 compound is preferably amorphous. Since the 1__80 compound is amorphous, the 1__80 compound exists as a buffer layer between the active material and the solid electrolyte, and the interface resistance can be further reduced. Whether the compound coating the surface of the core material particles is crystalline or amorphous can be judged by confirming whether or not a halo pattern can be obtained by selected area electron diffraction. A halo-battern is a low-angle, broad diffraction pattern with no distinct diffraction peaks.
- each element in the compound can be shown as, for example, !_ ⁇ , 80 ⁇ , if the element is at least one element of the 3 and 1 ⁇ 1 ⁇ .
- X and S in the formula can take arbitrary values within the range according to the valence of the element. Above all, for 1 mol of eight elements,! It is particularly preferable that the composition has a composition containing more than 1 mol of _ (father> 1). By doing so, it is possible to suppress the formation of the compound of 8 and O and effectively reduce the interface resistance.
- the core particle is not particularly limited as long as it functions as an active material.
- the core material particles may include, for example, a lithium metal composite oxide.
- a lithium metal composite oxide a known lithium metal composite oxide can be used.
- a lithium-containing complex oxide with a layered rock-salt structure represented by the general formula 1_ ⁇ 1 ⁇ /1 ⁇ 2 (IV! is a metallic element
- Lithium-containing composite oxide, general formula (IV! is a metal element) or 1_ ⁇ 1 ⁇ /1 3 1 0 4 (IV! is a metal element), and any one or a combination of two or more of the olivine-structured lithium-containing composite oxides. It may be. However, it is not limited to these.
- the core particles are! _ ⁇ , IV! n and 0, and particles of spinel-type composite oxide containing one or more, preferably two or more elements other than these, are preferable. Is also referred to as "core material particle eight.”).
- the active material of the present invention containing the core particle 8 When used as the positive electrode active material, it has an operating potential of 4.5 V or more in terms of metal standard potential.
- Metal !_ has a working potential of 4.5 or more at reference potential” means that it is not necessary to have only a working potential of 4.5 V or more as a plateau region, and a working potential of 4.5 V or more is required. It also includes the case where a part of the electric potential is included.
- the present invention is not limited to the positive electrode active material composed only of the 5 V class positive electrode active material having an operating potential of 4.5 or more as the plateau region.
- the active material of the present invention may include a positive electrode active material having an operating potential of 4.5 as a plateau region. Specifically, ⁇ 0 2020/175 506 10 (: 170? 2020 /007578
- the V-class positive electrode active material accounts for 30% by mass or more, preferably 50% by mass or more, and particularly preferably 80% by mass or more (including 100% by mass). Is tolerated.
- the core particle 8 is! It is preferable that the particles are made of a spinel-type composite oxide containing Mn and ⁇ and two or more kinds of elements other than these. At least one element of “two or more elements other than these” is preferably a metal element IV! 1 selected from the group consisting of 1 ⁇ ! and ⁇ and 6, and the other one element is N 3, IV! 9, 8 I,, [ ⁇ , ⁇ 3, Ding I, V, ⁇ “, 6, ⁇ , ⁇ ri, ⁇ , ⁇ , “, It is preferable that the metal element IV! 2 is composed of one kind or a combination of two or more kinds selected from the group consisting of ⁇ and ⁇ 6.
- the metal element IV! 1 is a substitution element that mainly contributes to the development of an operating potential of 4.5 V or more at the metal !_ ⁇ reference potential, and 1 ⁇ 1 and XX and 6 are listed. However, it is only necessary to contain at least one of these elements, and it is particularly preferable to contain at least one element selected from 1 ⁇ 1 and 000.
- the metal element IV! 2 is a substitution element which mainly contributes to stabilizing the crystal structure and enhancing the characteristics.
- a substitutional element that contributes to improving the capacity retention rate for example, N 8, 1 ⁇ /19, 8 ⁇ , [ ⁇ , D, V, ⁇ ”, ⁇ , ⁇ ⁇ , ⁇ re, ⁇
- the metallic element IV! 2 may be one or a combination of two or more of the above-mentioned elements.
- the metal element IV! 2 preferably contains at least one of the above-mentioned elements, and may contain a metal element other than the above-mentioned elements. ⁇ 02020/175506 11 ⁇ (: 170? 2020 /007578
- the metal element IV! 2 contained in the structure is a different element species from the metal element IV! 1.
- equation (1) 1_ ⁇ X
- "X” is ...! .00 or more! It is preferably .20 or less, more preferably 1.01 or more or 1.10 or less, and even more preferably 1.02 or more or 1.08 or less.
- “V”, which indicates the content of metallic element IV! 1, is ⁇ .20 or more! It is preferably .20 or less, more preferably ⁇ .30 or more or 1.10 or less, and even more preferably ⁇ .35 or more or 1.05 or less. It is preferable that the value “A” indicating the content of the metal element IV! 2 is ⁇ 0.001 and ⁇ 400.
- it is 002 or more or ⁇ .400 or less, of which 0.005 or more or 0.30 or less, and more preferably ⁇ 10 or more. Particularly, by setting it to 0.10 or more, the cycle characteristics can be more effectively improved.
- the formula (2) - general formula [!_ ⁇ X (1 ⁇ 1 ⁇ 3 2 -5 ] and a spinel-type lithium manganese-containing composite oxide.
- “X” is 1.00 or more 1.
- “So” is preferably 0.20 or more and ⁇ .70 or less, particularly ⁇ .30 or more or ⁇ .60 or less, and ⁇ .35 or more or 0.55 or less among them. It is even more preferred to be present.
- the metal element IV! 3 may be, for example, N 3, IV! 9 , 8 ⁇ , [ ⁇ , 03 % ⁇ , V, ⁇ ‘ ⁇
- the metal element M3 may be one kind or a combination of two or more kinds of the above-mentioned elements. “Z” indicating the molar ratio of the metal element M3 is preferably larger than 0 and not more than 0.5, more preferably not less than 0.01 or not more than 0.45, and even more preferably not less than 0.55 or 0. It is even more preferably 0.40 or less, more preferably 0.10 or more or 0.35 or less. In particular, by setting it to 0.10 or more, the cycle characteristics can be improved more effectively.
- S is preferably 0 or more or 0.2 or less, more preferably 0.1 or less, and most preferably 0.05 or less.
- the core material particles A may contain components other than the above Li, Mn, metal element M 1, metal element M 2, metal element M 3 and ⁇ .
- other elements may be contained as long as they are 0.5% by weight or less, respectively. This is because it is considered that the amount of this amount has almost no effect on the performance of the core material particles.
- the core material particles A may contain B (boron).
- the existing state of B may include a complex oxide phase containing Ni, Mn and B in addition to the spinel crystal phase.
- N i examples of the composite oxide phase containing M n and B, for example, N i 5 M n 0 4 (can be cited a crystal phase of Boy 2.
- the content of the complex oxide phase containing Ni, Mn and B should be 0.02% by mass or more and 0.80% by mass or less. It is preferable to contain the complex oxide phase in ⁇ 0 2020/175 506 13 ⁇ (: 170? 2020 /007578
- the complex oxide phase in an amount of 0.60 mass% or less, of which 0.30 mass% or less, and particularly 0.25 mass% or less. If the content of the Min element is 0.02 mass% or more, the discharge capacity at a high temperature (for example, 45 ° ⁇ can be maintained, and the content of the Min element is 0.80 mass% or less. This is preferable because rate characteristics can be maintained.
- the core material particles 8 are, for example, (0 r I 9 I n ⁇ ⁇
- the structure is a spinel structure.
- the primary particles of the core material particles 8 are preferably not a single crystal body but a polycrystal body.
- the single crystal means a particle in which a primary particle is composed of one crystallite
- the polycrystal means a particle in which a plurality of crystallites exist in the primary particle.
- the core particles are! _ ⁇ , IV! element (IV! is at least And a combination of one or more elements selected from the group consisting of 8 I. It is also preferable that the particles are composed of a lithium nickel metal composite oxide having a layered structure containing (1) and () (hereinafter, the core particles are also referred to as “core particles”).
- the active material of the present invention may contain other components in addition to the core particle. However, from the viewpoint that the characteristics of the core particle can be effectively obtained, the core particle content is 80% by mass or more, 90% by mass or more, and 95% by mass or more (100% by mass) % Is included).
- the core material particle is represented by the general formula (3) (In the formula, IV! is 1 ⁇ 1 ⁇
- Equation (3) May contain the three elements 1 ⁇ / ⁇ , ⁇ and ⁇ .
- it may be composed of only three elements of Mn, 0.00, and ⁇ , the three elements may contain one or more kinds of the other elements, or may have another structure.
- transition metal elements existing between Group 3 elements and Group 11 elements of the Periodic Table and typical metal elements from the 1st to 3rd periods of the Periodic Table include
- the atomic ratio of oxygen content is described as “2” for convenience, but it may have some non-stoichiometry. That is, the atomic ratio of oxygen content may be "2-5", in which "1-5" indicates oxygen deficiency, and 5 is preferably 0 or more or 0.2 or less. Above all, it is less than 0.1, and even more preferably below 0.05.
- the core material particle may contain unavoidable impurities.
- each element of unavoidable impurities may be contained in an amount of 0.17% by mass or less. This is because it is considered that the amount of this amount has almost no effect on the characteristics of the core particle.
- the core particle M represents, for example, the degree of agreement between the observed intensity and the calculated intensity when fitted with the hexagonal crystal structure model of space group 3,
- the primary particles of the core material particles are preferably not a single crystal body but a polycrystal body.
- the definition of single crystal and polycrystal is the same as that of the core particle 8.
- the active material of the present invention preferably has the following features.
- the primary particles of the active material of the present invention are preferably polycrystalline rather than single crystalline. Specifically, it is preferable that an amorphous amorphous compound is present on the surface of the core material particles that are polycrystalline.
- a single crystal means a particle in which a primary particle is composed of one crystallite, and a polycrystal means a particle in which a plurality of crystallites are present in the primary particle.
- the primary particles of the active material are not single-crystal, that is, whether they are polycrystalline or not is determined by the ratio of the crystallite size to the average _ primary particle diameter (crystallite size/average _ secondary particle diameter) being 0. It can be judged by confirming that it is close to, specifically, larger than 0 and smaller than 1. Close to 0 means that there are many crystallites in the primary particles. ⁇ 0 2020/175 506 16 ⁇ (: 170? 2020 /007578
- the term "primary particle” means 3 1 1//1 (scanning electron microscope, for example, 5
- the average primary particle size is 3 1//1 (scanning electron microscope, for example, 500 times or more and 500 times or less), and arbitrarily select 30 primary particles and The particle size of the selected primary particles can be calculated using analysis software, and the average particle size of 30 primary particles can be obtained.
- the “secondary particle” means a particle in which a plurality of primary particles are aggregated so as to share a part of their outer circumferences (grain boundaries) and are isolated from other particles. ..
- crystallite means a primary particle that can be regarded as a single crystal, It can be obtained by measuring and performing a Rietveld analysis.
- the mode diameter of the active material of the present invention is preferably 0.40 or more and 11.0 or less. Greater than 1 . ⁇ or less than 1 1 .01, among them ...! .0 0 0 greater than 1 or less than 1 0 0 0, especially greater than 1 .50 0 or less than 1 0 0 0, Further, among them, it is particularly preferable that it is greater than 2.001 or less than 9.0.
- Mouth 5 ⁇ by mouth 5 0, i.e. the volume particle size distribution measurement obtained by measuring Ri by the laser diffraction scattering particle size distribution measuring method of the active material of the present invention is preferably for example ⁇ . 5 or more, 1. It is preferably 0 or more, 2. ⁇ 02020/175506 17 ⁇ (: 170? 2020 /007578
- the mouth 50 is, for example, preferably 150 or less, more preferably 10.0 or less, and particularly preferably 8.0 or less.
- the percentage of the absolute value of the difference between the mode diameter and the mouth 50 with respect to the mode diameter (( ⁇ mode diameter _ 0 5 . ⁇ /mode diameter) X 1 ⁇ ⁇ ) is 0% £ ( (
- ⁇ / mode _ de diameter) X 1 00 it is preferable to satisfy (( ⁇ mode diameter over B 50 I / mode diameter) X 1 00) £ 20% , in particular ((I mode diameter _ port 50 I / mod diameter) X 100) It is preferable to meet £ 17%, and (( I mode diameter -50 I / mod diameter) X 100 ) It is preferable to satisfy £ 16%, and above all ((
- I/mode diameter) X 100 is preferably 0% ⁇ ((( mode diameter bit 5 1. 1/mode diameter) X 100), among which 1% £ (
- ⁇ / mode diameter) X 100 value in the above range means that the particle size distribution is unimodal, that is, it does not have multiple peaks. , It means a normal distribution or a distribution close to it.
- Mouth of the active material of the present invention ⁇ That is, it is preferable that the mouth 10 measured by the laser diffraction/scattering particle size distribution measurement method by volume particle size distribution measurement is, for example, 0.2 or more and 8.0 or less.
- the active material mouth 10 is 1. ⁇ 02020/175506 18 ⁇ (: 170? 2020 /007578
- the mouth 10 of the active material is preferably 6.0 or less, and particularly preferably 5.0 or less. mouth! By adjusting ⁇ within the above range, side reactions can be suppressed.
- the active material of the present invention has a mode diameter and a mouth diameter that are different from the mode diameter.
- the percentage of the absolute value of the difference with ⁇ ((
- (( ⁇ mode diameter _ ⁇ 10 ⁇ / mode diameter) XI 00) is preferably (( ⁇ mode diameter one bit ] ⁇ I / mode diameter) X 1 00) £55.0%, Especially (( ⁇ mode diameter bite!.
- / mode diameter) X 100) It is preferable to satisfy £45.0%, and further ((
- / mode diameter) X 100) can satisfy 1% £ ((
- /mode diameter) XI 00) in the above range means that the mode diameter of the active material is equal to the value! It means that the range of distribution up to ⁇ is narrow.
- the percentage of the absolute value of the difference between the mode diameter and the mouth 5 ⁇ ((
- the particles of the active material having a sharp particle size distribution have the coating layer containing the above-mentioned 1_O compound, the advantageous effect that the charging characteristics are improved can be obtained. Played.
- the active material manufacturing method described below the phenomenon of adsorption to the core particles is used when introducing the structure of the coating layer containing the above-mentioned 1_0 compound, so that a sharp particle with a uniform particle size is used.
- the coverage ratio and coating thickness of each particle can be leveled successfully, and the coating state of the particles is uniform for each particle, and the active material has a sharp particle size distribution. Particles are obtained. Due to this, the movement of lithium ions during charging is leveled for each particle, and the charging characteristics are improved.
- the volume average particle size distribution measured by the laser diffraction/scattering particle size distribution measurement method is, for example, preferably 0.1 or more, and more preferably 0.15 or more, and particularly 2 .. is preferably larger than .0, and more preferably larger than .0.6.
- it is preferably not more than 6.0, particularly preferably less than 5.0, particularly preferably less than 4.0, and further preferably less than 3.0. Further, among them, it is preferably 2.0 or less, and further preferably less than 1.8 IX. Side reactions can be suppressed and cycle characteristics can be improved.
- the average primary particle diameter of the active material of the present invention is preferably, for example, ⁇ .10 or more, and more preferably greater than ⁇ 25. In particular, it is preferable that it is larger than 0.40, and it is further preferable that it is larger than 0.50.
- the average primary ⁇ 2020/175506 20 20 (: 170? 2020/007578
- the particle size is, for example, preferably 5.0 or less, more preferably 4.00 or less, and particularly preferably 3.0 or less. When the average primary particle diameter is within the above range, improvement in rate characteristics can be achieved.
- the above ratio is preferably 0.1 or more, particularly preferably 0.2 or more, among them, preferably 0.3 or more, and further preferably 0.4 or more. ..
- the above ratio is preferably 0.9 or less, particularly preferably 0.85 or less, and particularly preferably 0.7 or less.
- Average primary particle size/mouth 5 By setting the above range, the dispersibility of the primary particles can be increased.
- each of the primary particles can sufficiently come into contact with the solid electrolyte. With this! _ As the reaction area between the particles and the particles increases, the resistance at the interface between the primary particles in the secondary particles can be reduced, which leads to the improvement of the end-of-life characteristics of the discharge.
- a firing temperature may be adjusted, or a substance such as a boron compound or a fluorine compound which enhances reactivity during firing may be used. It is preferable to produce an active material by adding and firing. However, it is not limited to this method.
- the active material of the present invention preferably has a crystallite size of, for example, 80 n or more and 490 n or less.
- the crystallite size is preferably 100 nm or more, particularly preferably 110 nm or more, further preferably 120 n or more, and among them, 130 mm or more. Is preferred.
- the crystallite size is preferably 350 n or less, and more preferably 240 n or less. To define the crystallite size within the above range ⁇ 0 2020/175 506 21 ⁇ (: 170? 2020 /007578
- the ionic conductivity in the crystallite can be increased and the resistance can be reduced. Further, by reducing the resistance, it is possible to suppress polarization during cycling, and it is possible to suppress a gradual decrease in discharge capacity that accompanies repeated charging and discharging at high temperatures.
- the ratio of the average primary particle size to the crystallite size is preferably, for example, 0.011 or more and 0.50 or less.
- the above ratio is preferably 0.02 or more, particularly preferably 0.03 or more, further preferably 0.04 or more, and among them, 0.05 or more. It is preferable.
- the above ratio is ⁇ .
- the active material of the present invention is preferably a polycrystal
- the crystallite size/average primary particle diameter is a value of less than 1, and within the above range, the primary particles in the powder are The dispersibility is improved, the contact area between the primary particles and the solid electrolyte is increased, and the resistance at the interface between the primary particles in the secondary particles can be reduced, which improves the end-of-discharge characteristics.
- the active material of the present invention has an X-ray diffraction pattern measured by an X-ray diffractometer ([0]), and the strain value obtained from the Rietveld analysis is, for example, ⁇ .
- the strain of the active material of the present invention is less than 0.35 among them, less than 0.32 among them, less than 0.30 among them, and further less than 0.28 among them, and among them with ⁇ . Less than .25, of which ⁇ . ⁇ 02020/175506 22 ⁇ (: 170? 2020 /007578
- heat treatment may be performed under preferable conditions. However, it is not limited to these methods.
- the active material of the present invention has a specific surface area, for example, from the viewpoint of suppressing side reactions.
- 1 0 12/9 or more 1 2. is 0 2/9 or less, preferably ⁇ . 20 12/9 greater than or 1 ⁇ . More preferably less than ⁇ 2/9, the inter alia 8.0 less than 2/9, further 7.0 less than 2/9 among them, it is more preferable in particular 5. hundred! 2 / less among them.
- the specific surface area of the active material of the present invention for example, 0.40 ⁇ / 9 or more or 1 2. ⁇ 2 /
- the specific surface area is measured as follows. First, sample 2.09 is weighed in a glass cell (standard cell) for a fully automatic specific surface area measuring device IV! 8 ⁇ 3 ⁇ “Tsubo (manufactured by Mountech Co., Ltd.), and set on a Saito Tosun Blur. After replacing the inside of the glass cell with gas, heat-treat in the nitrogen gas atmosphere at 200 ° for 15 minutes, and then cool for 4 minutes while flowing a nitrogen-helium mixed gas.After cooling, sample (powder) The mixed gas of nitrogen 30 V 0%% : helium 70% 0% is used for the adsorption gas during cooling and measurement.
- the ratio of !__ and element on the surface of the active material is controlled within a predetermined range.
- the ⁇ I ratio (1_ ⁇ /) of 1- ⁇ content to the element content on the surface of the active material (particles) obtained by X-ray photoelectron spectroscopy analysis (3) is 0.5 or more. 33.3 or less ⁇ 0 2020/175 506 23 ⁇ (: 170? 2020 /007578
- the ⁇ ratio (1- ⁇ /) is 0.5 or more and 3.5 or less, and in particular, it is greater than 0.7 or less than 3.4, in particular greater than 1.0 or It is preferably less than 3.0, more preferably more than 1.1 or less than 2.5, and still more preferably more than 1.2 or less than 2.1.
- the above-mentioned I ratio (1_ ⁇ /) is a value including 1_ ⁇ due to lithium carbonate.
- carbonate ion amount i.e. ⁇ 3_Rei 3 2 considered from carbonate -.. Amount is preferably 4 less than 0 wt% with respect to the active material of the present invention, among them 3 less than 0 wt%, the It is particularly preferably less than 2.5% by mass, more preferably less than 2.0% by mass, and most preferably less than 1.0% by mass.
- firing is performed in a carbon dioxide-free atmosphere such as an oxygen atmosphere, and more preferably, hydrolysis is performed while irradiating ultrasonic waves. preferable.
- the active material of the present invention is, for example,! _Shi IV! element (IV! is one or a combination of two or more elements selected from the group consisting of 0, IV! n and 8 I.
- the core material particles are added to a mixed solution of a lithium raw material and an element raw material dissolved in a solvent, followed by drying and firing under predetermined conditions.
- the core material particles are subjected to surface coating treatment by adding the core material particles to a mixed solution of a lithium raw material and an elemental raw material dissolved in a solvent, followed by drying and firing under predetermined conditions.
- these manufacturing methods are preferable examples, and the present invention is not limited to such manufacturing methods.
- the rolling fluid coating method sol-gel method
- mechanofusion method mechanofusion method
- XX method and V0 method can also be manufactured by adjusting the conditions.
- the method for producing the core particles there can be mentioned a production method including a raw material mixing step, a wet pulverizing step, a granulating step, a firing step, a heat treatment step, a washing/drying step and a pulverizing step.
- a production method including a raw material mixing step, a wet pulverizing step, a granulating step, a firing step, a heat treatment step, a washing/drying step and a pulverizing step.
- a manufacturing method is a preferable example, and the manufacturing method is not limited to such a manufacturing method.
- a core material particle powder is added to a mixed solution of a lithium raw material and an eight-element raw material dissolved in a solvent, It may be dried and fired under predetermined conditions. For example, by dissolving a water-soluble octo-element salt and a lithium raw material in water to prepare a surface treatment liquid, introducing core material particles into the surface treatment liquid, kneading the mixture to form a slurry, and drying it. It can be suitably manufactured.
- the method for producing the active material is not limited to such a method. For example, rolling fluid coating method (sol-gel method)
- the mechanofusion method, the ⁇ method and the ⁇ method can also be manufactured by adjusting the conditions.
- the active material of the present invention can be reduced, and the end-of-discharge characteristics and cycle characteristics can be improved.
- the method of simply spraying the complex solution on the active material particles serving as the core can obtain the above effects. May not be.
- the method of reducing !! is not limited to this method.
- the active material of the present invention can be usually used as a positive electrode active material. Further, the active material of the present invention is used for a solid state battery. In particular, the active material of the present invention is advantageously used in a solid battery containing a solid electrolyte as the solid electrolyte. In the solid state battery, the effect of the present invention can be enjoyed by the existence of the contact portion between the active material of the present invention and the solid electrolyte.
- “there is a contact portion between the active material and the solid electrolyte” means that (a) the solid electrolyte should be contained in the electrode mixture such as the positive electrode mixture (in this case, the solid electrolyte layer may be a sulfide.
- Non-sulphide is also possible.
- Electrode mixture such as positive electrode mixture does not contain solid electrolyte and solid electrolyte layer contains solid electrolyte
- electrode such as positive electrode mixture. This means that either the solid electrolyte is contained in the mixture, and the solid electrolyte is contained in the solid electrolyte layer.
- the electrode mixture of the present invention such as a positive electrode mixture contains an active material and a solid electrolyte.
- the active material contained in the electrode mixture can be the same as the content described in the above section ". Active material", and thus the description thereof is omitted here.
- the solid electrolyte used in the present invention may be the same as the solid electrolyte used in a general solid battery. Examples thereof include sulfide solid electrolytes, oxide solid electrolytes, nitride solid electrolytes, halide solid electrolytes, and the like. Among them, sulfide solid electrolytes containing a sulfur (3) element are preferable.
- the sulfide solid electrolyte in the present invention may be, for example, one containing a lithium (!_ ⁇ ) element and a sulfur (3) element and having lithium ion conductivity, or ⁇ 02020/175506 26 ⁇ (: 170? 2020 /007578
- the sulfide solid electrolyte may be any of crystalline materials, glass ceramics, and glass.
- the sulfide solid electrolyte may have a crystal phase having an aldyrodiite type structure.
- Such sulfide solid electrolytes include, for example, 1_ ⁇ 2 3_? 2 3 5 , 1_ ⁇ 2 3_? 2 3 5 _1_ 1
- the active material contained in the electrode mixture of the present invention may be only the active material of the present invention, or may be used in combination with other active materials.
- the other active material include particles made of the above-mentioned known lithium-transition metal composite oxide, and the particles may or may not have a coating layer.
- the active material of the present invention is contained in an amount of 50 mol% or more, more preferably 70% or more, based on the whole active material.
- the proportion of the sulfide solid electrolyte in the electrode mixture of the present invention is typically 5% by mass or more and 50% by mass or less.
- the electrode mixture may contain other materials such as a conductive auxiliary agent and a binder, if necessary.
- an electrode layer such as a positive electrode layer can be prepared by mixing an electrode mixture and a solvent to prepare a paste, applying the mixture on a current collector such as an aluminum foil, and drying.
- the solid battery of the present invention includes a positive electrode layer, a negative electrode layer, and a solid electrolyte layer, and the positive electrode layer contains the positive electrode mixture described above.
- the solid-state battery of the present invention can be produced, for example, by stacking three layers of the positive electrode layer, the solid electrolyte layer, and the negative electrode layer produced as described above under pressure.
- Solid-state battery means a solid substance that does not contain any liquid or gelled substance as an electrolyte. ⁇ 0 2020/175 506 27 ⁇ (: 170? 2020 /007578
- embodiments including, for example, 50% by mass or less, 30% by mass or less, and 10% by mass or less of a liquid substance or a gel substance as an electrolyte are also included.
- the negative electrode active material used for the negative electrode layer may be the same as the negative electrode active material used for general solid-state batteries.
- a specific negative electrode active material a material that absorbs and releases lithium ion, for example, a known material such as carbon material, silicon and silicon oxide compounds such as 3___, tin compounds, and lithium titanate is used. be able to.
- the carbon material include polyacrylonitrile, a phenol resin, a phenol novolac resin, a sintered material of an organic polymer compound such as cellulose, artificial graphite and natural graphite.
- the negative electrode layer can be produced in the same manner as the positive electrode layer except that such a negative electrode active material is used.
- An average particle diameter ( ⁇ 5 0) 7 of lithium carbonate, average particle size (0 5 ⁇ ) and 2 3 a specific surface area of 4 0 0 ⁇ / 9 of the electrolytic manganese dioxide, average particle size (0 5 ⁇ ) 2 2 Of nickel hydroxide and titanium oxide having an average particle size of (0 50 ) 2 were weighed.
- An aqueous solution of ammonium polycarboxylic acid salt (3 1 ⁇ 1 Dispersant 5 4 6 8 manufactured by San Nobuco Co., Ltd.) was added as a dispersant to ion-exchanged water.
- the weighed 1 ⁇ 1 IV!n raw material is added to the ion-exchanged water in which the dispersant has been dissolved in advance, mixed and stirred, and subsequently, a wet mill is used for 1300° , 1 2 0 minutes ground to an average particle diameter (mouth 5 0) was obtained ⁇ . 6 0 ground slurry follows. then, by adding the remaining ingredients in the slurry, and stirred, followed by 1 3 0 0 ", grind for 120 minutes to obtain an average particle size (0 50 ) of 0 ⁇ 0 2020/175 506 28 ⁇ (: 170? 2020 /007578
- a pulverized slurry of .60 or less was obtained.
- the solid content concentration at this time was 40 mass %.
- the obtained pulverized slurry is a hot spray dryer (spray dryer, manufactured by Okawara Kakoki Co., Ltd.). 0") was used for granulation and drying. At this time, a twin-jet nozzle was used for atomization, the atomization pressure was 0.46 1 ⁇ /1 3, and the slurry supply amount 3 4 n % Drying tower exit temperature 100. Granulation drying was performed by adjusting the temperature so that it was ⁇ or more and 110° or less.
- the obtained granulated powder was calcined in a static electric furnace in an air atmosphere so as to hold 900 ° ⁇ for 37 hours, and then crushed by a crusher (Orient rigid crusher, Orient It was crushed with a crusher (manufactured by Co., Ltd.).
- the disintegrated using a stationary electric furnace, in air atmosphere, 7 5 0 ° ⁇ heat-treated to hold 3 7 hours (first heat treatment), disintegrator (Orient Ken type powder mill, Orient crusher (Made by a corporation).
- the mixture was put into a plastic beaker (capacity 500 0 !_) containing 1 to 16 or more and 7 or less and a temperature of 25 ° ⁇ and ion-exchanged water 200 0 !_.
- a propeller area of 3300! 2 the mixture was stirred for 40 minutes at 40 0 " ⁇ 1 or more and 5 50 0" or less.
- the stirring was stopped and the stirrer was taken out of the water.
- the supernatant was removed by decantation, and the remaining sediment was collected using a suction filter (filter paper 1 ⁇ 10. 1 31 1), and the collected sediment was collected 1 2 It was dried in an environment of 0 ° for 12 hours, and then dried for 7 hours while being heated so that the product temperature was 500°.
- the powder after the second heat treatment is classified with a sieve with a mesh size of 53, and the bottom of the sieve is collected and reprocessed. ⁇ 02020/175506 29 ⁇ (: 170? 2020 /007578
- a um-manganese-containing composite oxide was prepared. As described later, this lithium manganese-containing composite oxide was identified by measurement to be a spinel-type lithium manganese-containing composite oxide. The same applies to the following examples and comparative examples.
- the temperature during the firing and the heat treatment is the temperature of the processed product measured by bringing a thermocouple into contact with the processed product in the furnace.
- Example described later ⁇ Comparative example is the same
- An aqueous solution was obtained by dissolving 1_5 1 of 13.5 9 1 to 1.1 to 1 2 0 and ammonium peroxoniobate 29.39 containing fluorine in water of 5861_. This water solution I got a crystal.
- the core material particles 109 obtained in the above (1) were A slurry was prepared by adding it to an aqueous solution of lithium hydroxide 45 1_ whose concentration was adjusted to 1 1. 4 9 / 1_. The slurry was heated to 90° ⁇ or more, and 1_ _ _1 ⁇ 1 ⁇ _ ⁇ aqueous solution 1 5 1_ was added thereto. 1_ ⁇ 1 1 ⁇ 1 sq. 10 Aqueous solution is 1 _ ⁇ 1 1 ⁇ 1 sq. 10 crystals ⁇ .
- This sample has one peak in the range of 0.1 45 ⁇ ⁇ 1 or more ⁇ 0.1 85 ⁇ or less in the radial distribution function obtained by the measurement of X 8 3 and 0.28 01 ⁇ ⁇ ! or more ⁇ . There was also one peak in the range below 3 1 01 ⁇ !
- Example 1 heat treatment (second heat treatment) was performed in a tubular static furnace so that the holding time was maintained for 6 hours, and after drying at 1 30 ° ⁇ at the time of manufacturing the positive electrode active material, at 3 50 ° ⁇ A positive electrode active material was obtained in the same manner as in Example 1 except that the heat treatment was performed for 2 hours.
- This sample has one peak in the radial distribution function obtained by the measurement of X 8 3 in the range of 0. 1 45 doors or more and 0. 1 85 doors or less.
- Example 1 a static electric furnace was used to perform heat treatment (first heat treatment) so as to maintain 750° ⁇ for 38 hours in the air atmosphere, and after drying at 1 30° ⁇ during production of the positive electrode active material, A positive electrode active material was obtained in the same manner as in Example 1 except that heat treatment was performed at 500° for 2 hours.
- This sample has one peak in the range of 0.145 nm or more and 0.185 n or less in the radial distribution function obtained by the measurement of 8.3. It also had a single peak in the range below 3 10 mm.
- Example 1 a static electric furnace was used to perform heat treatment (first heat treatment) in an air atmosphere so as to maintain 750° ⁇ for 36 hours, and after drying at 1 30° ⁇ during production of the positive electrode active material, A positive electrode active material was obtained in the same manner as in Example 1 except that heat treatment was performed at 700° for 2 hours.
- This sample has one peak in the range of 0.145 nm or more and 0.185 n or less in the radial distribution function obtained by the measurement of 8.3. It also had a single peak in the range below 3 10 mm.
- the electrolytic manganese dioxide of and the nickel hydroxide having an average particle size of (0 50 ) 22 were weighed.
- a polycarboxylic acid ammonium salt aqueous solution (3! ⁇ 1 Dispersant 5468 manufactured by San Nobuco Co., Ltd.) was added to the ion-exchanged water as a dispersant.
- ⁇ 02020/175506 31 ⁇ (: 170? 2020 /007578
- the amount of dispersant added is the same as above! -It was made to be 6% by mass with respect to the total of the raw materials, the raw materials and the IV! n raw materials, and sufficiently dissolved and mixed in the ion exchange water.
- the weighed raw materials were added to the ion-exchanged water in which the dispersant was dissolved in advance, and mixed and stirred to prepare a slurry having a solid content concentration of 40% by mass.
- the obtained pulverized slurry is a hot spray dryer (spray dryer, manufactured by Okawara Kakoki Co., Ltd.). 0") was used for granulation and drying. At this time, a twin jet nozzle was used for spraying, and the spray pressure was 0.1 Slurry supply amount 35 n % Drying tower exit temperature 100. Granulation drying was performed by adjusting the temperature so that it was ⁇ or more and 110° or less.
- the obtained granulated powder was subjected to oxygen partial pressure ⁇ .
- calcination was carried out so that 950° was maintained for 37 hours, and then heat treatment was carried out so that 750° was maintained for 37 hours in an atmosphere with an oxygen partial pressure of 0.02 11 1 ⁇ /1 3.
- the calcined powder obtained by the heat treatment was classified with a sieve having openings of 53, and the powder under the sieve was collected to obtain a spinel type lithium manganese-containing composite oxide powder, that is, a positive electrode active material (sample).
- a spinel type lithium manganese-containing composite oxide powder was prepared.
- a chemical analysis of the obtained spinel-type lithium-manganese-containing composite oxide powder was carried out.
- This sample has a radial distribution function obtained by the measurement of X 8 3 ⁇ .1 45 ⁇ ! The following ranges, and ⁇ .
- the port 50 of the recovered layered lithium metal oxide powder that is, the core material particles, was 6.8. Cross-section of primary particles III. Photo! It was confirmed from the photograph that the core particles were polycrystalline.
- the positive electrode active material was obtained by drying at 310 ° by a spray dry granulation method.
- a positive electrode active material was obtained in the same manner as in Example 1 except these. This sample is more than 0.145 n in the radial distribution function obtained by measuring X 83. There was one peak in the following range, and one peak in the range of 0.2081 ⁇ 111 or more and 0.301 n or less.
- Example 5 a layered lithium metal oxide 0 50 powder i.e. core particles child was recovered was 2.4 Rei_1. Drying was carried out at 320° ⁇ by the spray dry granulation method, and further vacuum drying was carried out at 120° ⁇ for 2 hours.
- a positive electrode active material was obtained in the same manner as in Example 5 except for the above. This sample has one peak in the radial distribution function obtained by measurement of ⁇ 8 3 in the range of 0.145 nm or more and 0.185 n or less, and ⁇ 280 or more and ⁇ 0.31 or less There was one peak in the range.
- Example 5 ammonium peroxoniobate 59 and lithium hydroxide .709 were dissolved in ion-exchanged water 100!_ to prepare a surface treatment solution.
- This surface treatment liquid is called a treatment liquid tank.
- the lithium raw material reacts with the ammonium peroxoniobate in the solution. This makes it easy to adsorb onto the surface of core particles 1- A compound is formed on the surface of the core particles. After that, it was dried in a hot-air oven at 120 ° ⁇ and heat-treated at 500 ° ⁇ for 5 hours.
- a positive electrode active material was obtained in the same manner as in Example 5 except for the above. This sample has no peak in the range of 0.145 nm or more and 0.185 or less in the radial distribution function obtained by the measurement of VIII. It had one peak in the range of 310 n or less.
- an automatic sample feeder for a laser diffraction particle size distribution measuring device manufactured by Microtrac Bell Co., Ltd. "1 ⁇ /1 ⁇ ⁇ " ⁇ Using 30(3), put the sample (powder) in the water-soluble solvent, irradiate 40 ultrasonic waves multiple times for 360 seconds at a flow rate of 40%, and then use laser diffraction measuring the particle size distribution using a particle size distribution measuring instrument "1 ⁇ / 1 chome 300011", Chiyato the resulting volume-based particle size distribution Karamo - de diameter was measured ⁇ 50 and ⁇ 10.
- the number of times of ultrasonic wave irradiation was the number of times until the rate of change of the mouth 50 before and after ultrasonic wave irradiation was 8% or less.
- the water-soluble solvent used in the measurement was passed through a 60 filter, the "solvent refractive index” was 1.33, the particle permeability condition was "transmitted”, the particle refractive index was 2.46, and the "shape" was "non-spherical".
- the measurement range was set to 0.133 or more and 704.0 or less, and the measurement time was set to 30 seconds.
- the average primary particle diameters of the positive electrode active materials obtained in Examples and Comparative Examples were measured as follows.
- the sample (powder) was observed at 1 000 times, and selecting the size of the particles corresponding to the mouth 5 ⁇ .
- the magnification was changed to 20000 or more and 10000 or less, and the image was taken.
- An example of the magnification is mouth 5 . When the value is about 7, it is 10000 times, when it is about 15 it is 5 000 times, and when it is about 22, it is 2000 times, and it is an image suitable for obtaining the average primary particle size in the image analysis software described later. Can be taken.
- the average primary particle diameter, cumulative 50% particle diameter on volume distribution is that of (1-1 6 7 ⁇ Rei_rei_1 diameter circle equivalent diameter).
- the average primary particle diameter it is preferable to measure 30 or more primary particles and calculate the average value. If the measured number is insufficient, taken by adding selecting the size of the particles corresponding to the mouth 5 0, a total of primary particles was measured to be 3 0 than on.
- the crystal structure was identified as follows using an X 8 mouth device.
- the core material particle it is attributed to the hexagonal crystal of the space group _ 301, 1_ ⁇ in 3 3 sites, 1 ⁇ 1 ⁇ , ⁇ ⁇ , IV! IV! It is assumed that ⁇ is occupied in an excess of 1 _ ⁇ , 60 sites, and the seat occupancy rate and atomic displacement parameter of 3 3, 3 and 60 sites are set to 1, and the observed intensity and the calculated intensity are calculated. It represents the degree of agreement [3 ⁇ 4, repeated calculations were performed until 3 converged.
- Scattering slit Open
- Light receiving slit Open
- Offset angle 0 °
- the X-ray diffraction pattern for determining the crystallite size was measured using an X-ray diffractometer (D8 ADV ANCE manufactured by Bruker AXS KK) using Cu _Ka line under the following measurement conditions 2. I went.
- the crystal structure was assigned to a cubic crystal of the space group F d _3m (Origin Choice 2), and L i was present at the 8 a site, and the 16 d site was present. Mn, metallic element M 1, metallic element M 2, and excess L i are present in
- the hexagonal crystals of the space group R— 3 m (Origin Choice 2) are assigned, and L i is at the 3a site, N i, C ⁇ , Mn is at the 3b site. , M element and excess L i, and occupy 6 c sites, ⁇ is assumed to be occupied, and the seat occupancy and atomic displacement parameter B of 3 a and 3 b sites are set to 1 and 6 c sites.
- the fractional coordinate and the seat occupancy rate were changed and repeated calculations were performed until Rw p and GO F, which represent the degree of agreement between the observed intensity and the calculated intensity, converged.
- the crystallite size was calculated by analysis using a Gaussian function.
- a positive electrode mixture was prepared using the positive electrode active material and solid electrolyte prepared in Examples and Comparative Examples, and a solid lithium secondary battery (solid Gr/positive electrode active material cell) was prepared, and battery characteristics were evaluated. It was
- the positive electrode active materials prepared in Examples and Comparative Examples were used, the negative electrode active material was graphite (G r) powder, and the solid electrolyte powder was sulfide solid electrolyte having an aldirodite structure. ..
- the positive electrode mixture powder is the positive electrode active material, the solid electrolyte powder and the conductive material (force carbon material) produced in the examples and comparative examples.
- the powder is mixed in a mortar in a ratio of 60% by mass: 30% by mass: 10% by mass. I adjusted it by doing.
- the negative electrode mixture powder was prepared by mixing graphite (G r) powder and solid electrolyte powder in a mortar mixture at a ratio of 50% by mass: 50% by mass.
- a positive electrode mixture powder pellet was prepared by filling 13 mg of the positive electrode mixture powder (sample) into the insulating cylinder (09 mm) of a closed cell and uniaxially molding at 368 MPa. The positive electrode mixture powder pellets obtained were placed in an insulating cylinder of a closed cell ( ⁇ 10.
- solid electrolyte powder was axially molded at 1 84 M Pa together with the positive electrode material mixture powder pellets. Further, 10 mg of the negative electrode mixture powder was filled on the solid electrolyte, uniaxially molded at 55 1 MPa, and tightened with a pressure screw to provide a positive electrode layer, a negative electrode layer, and a solid electrolyte layer.
- a solid-state battery solid-state lithium secondary battery
- the solid-state batteries of Examples 1 to 4 were subjected to constant current charging at a charge end voltage of 5.0 V at ⁇ 0.10 in the first cycle. After that, constant voltage charging was performed until the current value reached 0.010 at 5.0.
- the capacity obtained by constant-current charging until reaching 5.0 V was defined as the XX capacity.
- the value obtained by multiplying 100 by the value obtained by dividing the capacity by the total charging capacity in the first cycle was used as the charging characteristic.
- the value obtained by subtracting the charge characteristic of Comparative Example 1 from the charge characteristics of Examples 1 to 4 was divided by the charge characteristic of Comparative Example 1 and multiplied by 100, and the value obtained thereby was used as the charge characteristic improvement index. , Listed in Table 1.
- the charge characteristic improvement index shows the improvement rate of the mobility (desorption property) of lithium ions during charging, and the charge characteristic improvement index can be used to evaluate rapid charging.
- the solid-state batteries of Examples 5 to 7 were subjected to constant current charging at a charge end voltage of 4.5 V at 0.30 in the first cycle. After that, constant voltage charging was performed at a voltage of 4.5 V until the current value reached 0.01. With respect to the charging characteristics of Comparative Example 2, the charging characteristic improvement indexes of Examples 5 to 7 were calculated in the same manner as in Examples 1 to 4, and are shown in Table 1.
- FIG. 3 shows the radial distribution function obtained by the X-83 measurement for the positive electrode active material of Example 3.
- an active material having improved desorption of lithium ions during charging. Therefore, by using the active material of the present invention, solid-state batteries can be rapidly charged.
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JP2021502292A JP6940716B2 (ja) | 2019-02-27 | 2020-02-26 | 活物質、それを用いた正極合剤及び固体電池 |
CN202080012950.XA CN113396495B (zh) | 2019-02-27 | 2020-02-26 | 活性物质、使用了该活性物质的正极合剂和固体电池 |
US17/431,907 US20220149354A1 (en) | 2019-02-27 | 2020-02-26 | Active material, positive electrode mixture using same, and solid-state battery |
KR1020217027647A KR102376785B1 (ko) | 2019-02-27 | 2020-02-26 | 활물질, 그것을 사용한 정극 합제 및 고체 전지 |
EP20762064.2A EP3933979A4 (en) | 2019-02-27 | 2020-02-26 | ACTIVE MATERIAL, POSITIVE ELECTRODE MIXTURE WITH IT AND SOLID STATE BATTERY |
US17/987,974 US20230074796A1 (en) | 2019-02-27 | 2022-11-16 | Active Material, Positive Electrode Mixture Using Same, And Solid-State Battery |
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JP2020140839A (ja) * | 2019-02-27 | 2020-09-03 | 三井金属鉱業株式会社 | 活物質、それを用いた正極合剤及び固体電池 |
JP2020140837A (ja) * | 2019-02-27 | 2020-09-03 | 三井金属鉱業株式会社 | 活物質、それを用いた正極合剤及び固体電池 |
EP4122890A1 (en) * | 2021-07-23 | 2023-01-25 | Samsung SDI Co., Ltd. | Positive active material for an all-solid-state battery, method of preparing the same, and all-solid-state battery |
US11569503B2 (en) | 2016-07-20 | 2023-01-31 | Samsung Sdi Co., Ltd. | Nickel-based active material for lithium secondary battery, method of preparing the same, and lithium secondary battery including positive electrode including the nickel-based active material |
WO2023140288A1 (ja) * | 2022-01-20 | 2023-07-27 | 住友金属鉱山株式会社 | 被覆付きリチウム二次電池用正極活物質、リチウム二次電池 |
US11742482B2 (en) | 2016-07-20 | 2023-08-29 | Samsung Sdi Co., Ltd. | Nickel-based active material for lithium secondary battery, method of preparing the same, and lithium secondary battery including positive electrode including the nickel-based active material |
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KR20210105254A (ko) * | 2020-02-18 | 2021-08-26 | 삼성에스디아이 주식회사 | 음극 및 이를 포함하는 전고체 이차전지 |
CN116799337B (zh) * | 2023-08-21 | 2024-01-23 | 深圳海辰储能控制技术有限公司 | 正极片、补钠颗粒分布均匀的确定方法及储能装置 |
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US20230074796A1 (en) | 2023-03-09 |
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CN113396495B (zh) | 2022-06-07 |
KR102376785B1 (ko) | 2022-03-21 |
US20220149354A1 (en) | 2022-05-12 |
KR20210112393A (ko) | 2021-09-14 |
JPWO2020175506A1 (ja) | 2021-09-13 |
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