Lithium ion secondary battery cathode material, lithium ion secondary battery cathode and lithium ion secondary battery that use same, and method for manufacturing lithium ion secondary battery cathode material

1. A cathode material for lithium ion secondary battery, made from an agglomerate including secondary particles formed via aggregation of primary particles of a lithium metal composite oxide having a layered structure, represented by the following composition formula (I)

Li 1+x M1 1−x−y M2 y O 2   (I)

where x is a number satisfying a relationship of −0.1≤x≤0.3; y is a number satisfying a relationship of 0≤y≤0.1; M1 is at least one kind of an element selected from a group of Ni, Co, Mn; and M2 is at least one kind of an element selected from a group of Mg, Al, Ti, Zr, Mo, Nb, Fe, B, wherein

the secondary particles forming the agglomerate have a particle size D10, which corresponds to 10% in volume-based cumulative particle size distribution encompassed within the range from 0.5 μm to 10 μm, and simultaneously a particle size D90, which corresponds to 90% in volume-based cumulative particle size distribution encompassed within the range of more than 10 μm and equal to 50 μm or less, when analyzed by laser diffraction/scattering particle size distribution measurement; and

a mean porosity of the secondary particles having the particle size D90 is higher than a mean porosity of the secondary particles having the particle size D10.

2. The cathode material for lithium ion secondary battery described in claim 1 , wherein

the mean porosity of the secondary particles having the particle size D90 is in the range from 5% to 70%; and

the mean porosity of the secondary particles having the particle size D10 is in the range equal to 5% or less.

3. The cathode material for lithium ion secondary battery described in claim 1 , further comprising primary particles of a lithium metal composite oxide having a different crystal structure from the lithium metal composite oxide having the layered structure.

4. The cathode material for lithium ion secondary battery described in claim 3 , comprised of any one selected from:

the secondary particles formed via aggregation of the primary particles of the lithium metal composite oxide having the layered structure and the primary particles of the lithium metal composite oxide having the different crystal structure;

a combination of the secondary particles formed via aggregation of the primary particles of the lithium metal composite oxide having the layered structure and the secondary particles formed via aggregation of the primary particles of the lithium metal composite oxide having the different crystal structure; or

a combination of the secondary particles formed via aggregation of the primary particles of the lithium metal composite oxide having the layered structure;

the secondary particles formed via aggregation of the primary particles of the lithium metal composite oxide having the different crystal structure; and the secondary particles formed via aggregation of the primary particles of the lithium metal composite oxide having the layered structure and the primary particles of the lithium metal composite oxide having the different crystal structure.

5. A lithium ion secondary battery cathode comprising a cathode material for lithium ion secondary battery described in claim 1 .

6. A lithium ion secondary battery provided with a lithium ion secondary battery cathode described in claim 5 .

7. A method for manufacturing a cathode material for lithium ion secondary battery, comprising the steps of:

preparing primary particles of a lithium metal composite oxide having a layered structure, and further primary particles of a lithium metal composite oxide having a different crystal structure from the lithium metal composite oxide having the layered structure, wherein each of the lithium metal composite oxides is represented by the following formula (I)

Li 1+x M1 1−x−y M2 y O 2   (I)

where x is a number satisfying a relationship of −0.1≤x≤0.3; y is a number satisfying a relationship of 0≤y≤0.1; M1 is at least one kind of an element selected from a group of Ni, Co and Mn; and M2 is at least one kind of an element selected from a group of Mg, Al, Ti, Zr, Mo, Nb, Fe and B;

wet-granulating a first aggregate of secondary particles each having particle size distribution encompassed within the range from 0.5 μm to 10 μm via using the primary particles as well as a second aggregate of secondary particles each having particle size distribution encompassed within the range of more than 10 μm and equal to 50 μm or less via using the primary particles, wherein the wet-granulation of the second aggregate is performed at a higher drying rate or by using slurry with higher viscosity than the wet-granulation of the first aggregate;

mixing the first aggregate and the second aggregate thus granulated; and

preparing an agglomerate of secondary particles, wherein in the secondary particles, a particle size D10, which corresponds to 10% in volume-based undersize cumulative particle size distribution is encompassed within the range from 0.5 μm to 10 μm, and simultaneously a particle size D90, which corresponds to 90% in volume-based undersize cumulative particle size distribution is encompassed within the range of more than 10 μm and equal to 50 μm or less, when analyzed by laser diffraction/scattering particle size distribution measurement; and a mean porosity of the secondary particles having the particle size D90 is higher than a mean porosity of the secondary particles having the particle size D10.