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

Patent metadata

Field	Value
Publication number	US-2017110726-A1
Application number	US-201515129159-A
Country	US
Kind code	A1
Filing date	Mar 12, 2015
Priority date	Mar 28, 2014
Publication date	Apr 20, 2017
Grant date	—

Abstract

Provided is a precursor of a positive electrode active material containing, in a reduced amount, impurities which do not contribute to a charge/discharge reaction but rather corrode a firing furnace and peripheral equipment and thus having excellent battery characteristics and safety, and production method thereof. A method for producing a precursor of a positive electrode active material for nonaqueous electrolyte secondary batteries having a hollow structure or porous structure includes obtaining the precursor by washing nickel-manganese composite hydroxide particles having a particular composition ratio and a pore structure in which pores are present within the particles with an aqueous carbonate solution having a carbonate concentration of 0.1 mol/L or more.

First claim

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
obtaining the precursor by washing nickel-manganese composite hydroxide particles represented by the general formula (1) and having a pore structure in which pores are present within the particles, with an aqueous carbonate solution having a carbonate concentration of 0.1 mol/L or more,
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.

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 panicle 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 precursor of a positive electrode active material for nonaqueous electrolyte secondary batteries having a hollow structure or porous structure, the precursor consisting of
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 the precursor has a sulfate group content of 0.4% by mass or less and a sodium content of 0.035% by mass or less,
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.

9 . The precursor of the positive electrode active .material for nonaqueous electrolyte secondary batteries of claim 8 , wherein the precursor has a chlorine content of 0.1% by mass or less.

10 . 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 mixing step of mixing the precursor of the positive electrode active material for nonaqueous electrolyte secondary batteries of claim 8 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.

11 . The method for producing the positive electrode active material for nonaqueous electrolyte secondary batteries of claim 10 , wherein the lithium compound is at least one selected from a group consisting of a hydroxide, oxyhydroxide, oxide, carbonate, nitrate, and halide of lithium.

12 . A positive electrode active material for nonaqueous electrolyte secondary batteries, consisting of
lithium-nickel-manganese composite oxide particles represented by the general formula (2) and having a hollow structure or porous structure, wherein the positive electrode active material has a sulfate group content of 0.4% by mass or less and a sodium content of 0.035% by mass or less,
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).

13 . The positive electrode active material for nonaqueous electrolyte secondary batteries of claim 12 , wherein the positive electrode active material has a chlorine content of 0.05% by mass or less.

14 . A nonaqueous electrolyte secondary battery using the positive electrode active material for nonaqueous electrolyte secondary batteries of claim 1 .

Assignees

• Sumitomo Metal Mining Co

Inventors

• Aida Taira
• Toya Hiroyuki

Classifications

• C01P2002/52

  containing elements as dopants · CPC title

• C01G51/50

  of the type (MnO2)n-, e.g. Li(CoxMn1-x)O2 or Li(MyCoxMn1-x-y)O2 · CPC title

• C01P2002/50

  Solid solutions · CPC title

• C01G53/50

  of the type (MnO2)n-, e.g. Li(NixMn1-x)O2 or Li(MyNixMn1-x-y)O2 · CPC title

• C01P2006/80

  Compositional purity · CPC title