Nickel composite hydroxide and manufacturing method thereof, cathode active material for nonaqueous-electrolyte secondary battery and manufacturing method thereof, and nonaqueous-electrolyte secondary battery
US-2015364761-A1 · Dec 17, 2015 · US
US10547052B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10547052-B2 |
| Application number | US-201615739216-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 9, 2016 |
| Priority date | Jun 26, 2015 |
| Publication date | Jan 28, 2020 |
| Grant date | Jan 28, 2020 |
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The presently disclosed subject matter is directed to transition metal-containing composite hydroxides, their use, and manufacturing methods thereof. More particularly, the subject matter describes a positive electrode active material for a non-aqueous electrolyte secondary battery that uses a transition metal-containing composite hydroxide as a precursor and a manufacturing method thereof. In some embodiments, the non-aqueous electrolyte secondary battery uses a positive electrode active material for a non-aqueous electrolyte secondary battery as a positive electrode material.
Opening claim text (preview).
What is claimed is: 1. A transition metal-containing composite oxide that is a precursor to a positive electrode active material for a non-aqueous electrolyte secondary battery, comprising: secondary particles formed by aggregates of plate-shaped primary particles and fine primary particles that are smaller than the plate-shaped primary particles; the secondary particles having a center section formed by aggregates of the plate-shaped primary particles, and at least one layered structure formed on an outside of the center section, the at least one layered structure in which a low-density layer formed by aggregates of the plate-shaped primary particles and the fine primary particles, and a high-density layer formed by aggregates of the plate-shaped primary particles are layered; the high-density layer connected with the center section and/or another high-density layer by a high-density section formed inside the low-density layer by aggregates of the plate-shaped primary particles; and the secondary particles having an average particle size within a range 1 μm to 15 μm, and an index [(d90−d10)/average particle size] that indicates a particle size distribution of the secondary particles is 0.65 or less. 2. The transition metal-containing composite hydroxide according to claim 1 , wherein the transition metal-containing composite hydroxide has a composition that is expressed by a general formula (A): Ni x Mn y Co z M t (OH) 2+a (where x+y+z+t=1, 0.3≤x≤0.95, 0.05≤y≤0.55, 0≤z≤0.4, 0≤t≤0.1, 0≤a≤0.5, and M is at least one additional element selected from among Mg, Ca, Al, Ti, V, Cr, Zr, Nb, Mo, Hf, Ta and W). 3. The transition metal-containing composite hydroxide according to claim 2 , wherein the additional element(s) (M) is uniformly distributed inside the secondary particles and/or uniformly coated on a surface of the secondary particles. 4. A manufacturing method of the transition metal-containing composite hydroxide that is a precursor to a positive electrode active material for a non-aqueous electrolyte secondary battery of claim 1 , the method comprising forming a reaction aqueous solution by supplying a raw material aqueous solution including at least a transition metal and an aqueous solution including an ammonium ion donor into a reaction tank and performing a crystallization reaction; comprising: a nucleation process adjusting a pH value of the reaction aqueous solution to a value within a range 12.0 to 14.0 at a reference liquid temperature of 25° C., and generating nuclei; and a particle-growth process controlling a pH value of the reaction aqueous solution including the nuclei that are obtained in the nucleation process to a value that is lower than the pH value of the nucleation process and that is within a range 10.5 to 12.0 at a reference liquid temperature of 25° C., and causing the nuclei to grow; a reaction atmosphere in the nucleation process and in an initial stage of the particle-growth process being adjusted to be a non-oxidizing atmosphere in which an oxygen concentration is 5% by volume or less; after the initial stage of the particle-growth process, atmosphere control being performed at least one time in which the reaction atmosphere is switched from the non-oxidizing atmosphere to an oxidizing atmosphere having an oxygen concentration that is greater than 5% by volume by directly introducing oxidizing gas into the reaction aqueous solution while continuing the supply of the raw material aqueous solution, and is further switched from the oxidizing atmosphere to a non-oxidizing atmosphere having an oxygen concentration that is 5% by volume or less by directly introducing inert gas into the reaction aqueous solution while continuing the supply of the raw material aqueous solution. 5. The manufacturing method of the transition metal-containing composite hydroxide according to claim 4 , wherein the oxidizing gas and the inert gas are introduced by a diffusing pipe. 6. The manufacturing method of the transition metal-containing composite hydroxide according to claim 4 , wherein in the particle-growth process, the total amount of time during which the oxidizing gas is introduces is within a range 1% to 25% with respect to the total time of the particle-growth process. 7. The manufacturing method of the transition metal-containing composite hydroxide according to claim 4 , wherein the amount of time of the crystallization reaction in the initial stage of the particle-growth process is within a range 0.5% to 30% with respect to the total time of the particle-growth process. 8. The manufacturing method of the transition metal-containing composite hydroxide according to claim 4 , wherein the transition metal-containing composite hydroxide has a composition that is expressed by a general formula (A): Ni x Mn y Co z M t (OH) 2+a (where x+y+z+t=1, 0.3≤x≤0.95, 0.05≤y≤0.55, 0≤z≤0.4, 0≤t≤0.1, 0≤a≤0.5, and M is at least one additional element selected from among Mg, Ca, Al, Ti, V, Cr, Zr, Nb, Mo, Hf, Ta and W). 9. The manufacturing method of the transition metal-containing composite hydroxide according to claim 8 , further comprising a coating process after the particle-growth process that coats the transition metal-containing composite hydroxide with compounds that include at least part of the additional element(s) (M). 10. A manufacturing method of a positive electrode active material for a non-aqueous electrolyte secondary battery, comprising: a mixing process forming a lithium mixture by mixing the transition metal-containing composite hydroxide according to claim 1 with a lithium compound; and a calcination process calcining the lithium mixture formed in the mixing process in an oxidizing atmosphere at a temperature within the range 650° C. to 980° C. 11. The manufacturing method of the positive electrode active material for a non-aqueous electrolyte secondary battery according to claim 10 , wherein, in the mixing process, the lithium mixture is adjusted so that a ratio of a sum of the number of atoms of metals other than lithium included in the lithium mixture and the number of atoms of lithium is within a range 1:0.95 to 1.5. 12. The manufacturing method of the positive electrode active material for a non-aqueous electrolyte secondary battery according to claim 10 , further comprising a heat-treatment process before the mixing process that heat treats the transition metal-containing composite hydroxide at 105° C. to 750° C. 13. The manufacturing method of the positive electrode active material for a non-aqueous electrolyte secondary battery according to claim 10 , wherein the positive electrode active material for a non-aqueous electrolyte includes a layered hexagonal crystal type of lithium transition metal-containing composite oxide that is expressed by the general formula (B): Li 1+u Ni x Mn y Co z M t O 2 (where, −0.05≤u≤0.50, x+y+z+t=1, 0.3≤x≤0.95, 0.05≤y≤0.55, 0≤z≤0.4, 0≤t≤0.1, and M is at least one additional element selected from among Mg, Ca, Al, Ti, V, Cr, Zr, Nb, Mo, Hf, Ta and W).
Physical characteristics, e.g. porosity, surface area · CPC title
of the type (MnO2)n-, e.g. Li(NixMn1-x)O2 or Li(MyNixMn1-x-y)O2 · CPC title
obtained by SEM · CPC title
as layered products · CPC title
Li-accumulators · CPC title
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