Precursor of positive electrode active material for nonaqueous electrolyte secondary batteries and production method thereof and positive electrode active material for nonaqueous electrolyte secondary batteries and production method thereof

1. A method for producing a precursor of a positive electrode active material for nonaqueous electrolyte secondary batteries having a hollow structure or porous structure, the method comprising

providing nickel-manganese composite hydroxide particles represented by the general formula (1) and having a pore structure in which pores are present within the particles, wherein

Ni x Co y Mn z M t (OH) 2   General Formula (1)

where 0.2≤x≤0.8; 0≤y<0.3; 0.07<z≤0.8; 0≤t≤0.1; x+y+z+t=1; and M is at least one element selected from Mg, Ca, Ba, Sr, Al, Ti, V, Cr, Zr, Mo, Hf, Ta, and W;

washing the nickel-manganese composite hydroxide particles with an aqueous carbonate solution having a carbonate concentration of 0.1 mol/L or more and 1.50 mol/L or less, thereby obtaining the precursor.

2. The method for producing the precursor of the positive electrode active material for nonaqueous electrolyte secondary batteries of claim 1 , wherein a porosity measured by observing a cross-section of the nickel-manganese composite hydroxide particles is 15% or more.

3. The method for producing the precursor of the positive electrode active material for nonaqueous electrolyte secondary batteries of claim 1 , wherein

the aqueous carbonate solution is an aqueous solution of at least one selected from potassium carbonate, sodium carbonate, potassium bicarbonate, and sodium bicarbonate, and a pH of the aqueous carbonate solution is 11.2 or more.

4. The method for producing the precursor of the positive electrode active material for nonaqueous electrolyte secondary batteries of claim 1 , wherein the nickel-manganese composite hydroxide particles are washed with the aqueous carbonate solution having a temperature of 15 to 50° C.

5. The method for producing the precursor of the positive electrode active material for nonaqueous electrolyte secondary batteries of claim 1 , wherein the nickel-manganese composite hydroxide particles are obtained by effecting neutralization and crystallization by charging a mixed aqueous solution of a metal compound containing nickel and manganese and optionally cobalt and the element M and an aqueous solution containing an ammonium ion donor into a warmed reaction vessel while adding, to a reaction solution, a sufficient amount of an aqueous alkali metal hydroxide solution to maintain alkalinity as necessary, and

in the neutralization crystallization, a nuclei formation step of forming nuclei and a particle growth step of growing the formed nuclei are separately performed by controlling a pH value of the reaction solution.

6. The method for producing the precursor of the positive electrode active material for nonaqueous electrolyte secondary batteries of claim 5 , wherein

the pH value in the nuclei formation step is controlled so as to become 12.0 to 14.0 at a reference solution temperature of 25° C., and

the pH value in the particle growth step is controlled so as to become 10.5 to 12.5 at a reference solution temperature of 25° C. and to be lower than the pH value in the nuclei formation step.

7. The method for producing the precursor of the positive electrode active material for nonaqueous electrolyte secondary batteries of claim 6 , wherein the mixed aqueous solution contains a chloride of at least one of nickel, manganese, and cobalt.

8. A method for producing a positive electrode active material for nonaqueous electrolyte secondary batteries, the positive electrode active material consisting of lithium-nickel-manganese composite oxide that is represented by the general formula (2) and has a hollow structure or porous structure, the method comprising:

a step of producing the precursor by the method according to claim 1 ;

a mixing step of mixing the precursor with a lithium compound to obtain a lithium mixture; and

a firing step of firing the lithium mixture in an oxidizing atmosphere at 800 to 1100° C. to obtain lithium-nickel-manganese composite oxide,

Li a Ni x Co y Mn z M t O 2   General Formula (2)

where 0.95≤a≤1.20; 0.2≤x≤0.8; 0≤y<0.3; 0.07<z≤0.8; 0≤t≤0.1; x+y+z+t=1; and M is at least one element selected from Mg, Ca, Ba, Sr, Al, Ti, V, Cr, Zr, Mo, Hf, Ta, and W.

9. The method for producing the positive electrode active material for nonaqueous electrolyte secondary batteries of claim 8 , wherein the lithium compound is at least one selected from a group consisting of a hydroxide, oxyhydroxide, oxide, carbonate, nitrate, and halide of lithium.

10. The method for producing the precursor of the positive electrode active material for nonaqueous electrolyte secondary batteries of claim 1 , wherein the nickel-manganese composite hydroxide particles are washed so that the precursor has a sulfate group content of 0.4% by mass or less.

11. The method for producing the precursor of the positive electrode active material for nonaqueous electrolyte secondary batteries of claim 1 , wherein the nickel-manganese composite hydroxide particles are washed so that the precursor has a sodium content of 0.035% by mass or less.

12. The method for producing the precursor of the positive electrode active material for nonaqueous electrolyte secondary batteries of claim 1 , wherein the nickel-manganese composite hydroxide particles are washed so that the precursor has a chlorine content of 0.1% by mass or less.