Lithium transition metal-based compound powder for positive electrode material in lithium rechargeable battery, method for manufacturing the powder, spray dried product of the powder, firing precursor of the powder, and positive electrode for lithium rechargeable battery and lithium rechargeable battery using the powder

1. A powder of a lithium transition-metal compound for a positive-electrode material in a lithium secondary battery, comprising:

a lithium transition-metal compound, as a main component, capable of intercalating and deintercalating lithium ions;

wherein the powder is prepared by (a) incorporating at least one additive, that inhibits grain growth and sintering during firing in the main component, in an amount greater than or equal to 0.01 mol % and less than 2 mol % with respect to the total molar amount of the transition-metal elements in the main component, and then (b) performing firing;

wherein the atomic ratio of the total amount of the additive element to the total amount of metal elements except Li and the additive element on surfaces of primary particles of the lithium transition-metal compound is 5 to 150 times the atomic ratio of the total amount of the additive element to the total amount of the metal elements except Li and the additive element in the entire particles of the lithium transition-metal compound; and

wherein the lithium transition-metal compound is a lithium-nickel-manganese-cobalt composite oxide that has a crystal structure which has a layered structure and is represented by formula (I″):

LiMO 2   (I″)

where the ratio of Li to M is in the range of 0.001 to 0.2 and M is represented by formula (II″):

M=Li z″/(2+z″) {(Ni (1+y″)/2 Mn (1−y″)/2 ) 1−x″ Co x″} 2/(2+z″)   (II″)

where 0≦x″≦0.1, −0.1≦y″≦0.1, and (1−x″)(0.0531 0.98y″)≦z″≦(1−x″)(0.20−0.88y″).

2. The powder of the lithium transition-metal compound for a positive-electrode material in a lithium secondary battery according to claim 1 , wherein the additive is an oxide that contains at least one element selected from the group consisting of Mo, W, Nb, Ta, and Re.

3. The powder of the lithium transition-metal compound for a positive-electrode material in a lithium secondary battery according to claim 1 , wherein the median diameter of the powder of the lithium transition-metal compound is in the range from 0.1 μm to 3 μm and is determined from volume-based particle diameters measured with a laser diffraction/scattering particle size distribution analyzer using the refractive index set at 1.24, and the measurement is made after a five-minute ultrasonic dispersion.

4. The powder of the lithium transition-metal compound for a positive-electrode material in a lithium secondary battery according to claim 1 , wherein the primary particles have an average diameter of 0.1 μm to 0.9 μm.

5. The powder of the lithium transition-metal compound for a positive-electrode material in a lithium secondary battery according to claim 1 , wherein the BET specific surface area of the powder of the lithium transition-metal compound is in the range of 1.5 m 2 /g to 5 m 2 /g.

6. The powder of the lithium transition-metal compound for a positive-electrode material in a lithium secondary battery according to claim 1 , wherein in a mercury intrusion curve obtained by mercury intrusion porosimetry of the powder of the lithium transition-metal compound, the amount of mercury intruded is in the range of 0.7 cm 3 /g to 1.5 cm 3 /g when the pressure is increased from 3.86 kPa to 413 MPa.

7. The powder of the lithium transition-metal compound for a positive-electrode material in a lithium secondary battery according to claim 1 , wherein a pore-size distribution curve obtained by mercury intrusion porosimetry of the powder of the lithium transition-metal compound has at least one main peak with a peak top that is present at a pore radius of 300 nm to 1,000 nm and does not have a sub-peak with a peak top that is present at a pore radius greater than or equal to 80 nm and less than 300 nm.

8. The powder of the lithium transition-metal compound for a positive-electrode material in a lithium secondary battery according to claim 1 , wherein in a pore-size distribution curve obtained by mercury intrusion porosimetry of the powder of the lithium transition-metal compound, a peak with a peak top that is present at a pore radius of 300 nm to 1,000 nm has a pore volume of 0.4 cm 3 /g to 1 cm 3 /g.

9. The powder of the lithium transition-metal compound for a positive-electrode material in a lithium secondary battery according to claim 1 , wherein the bulk density of the powder of the lithium transition-metal compound is in the range of 0.5 g/cm 3 to 1.7 g/cm 3 .

10. The powder of the lithium transition-metal compound for a positive-electrode material in a lithium secondary battery according to claim 1 , wherein the volume resistivity of the powder of the lithium transition-metal compound that is compacted at a pressure of 40 MPa is in the range of 1×10 3 Ω·cm to 1×10 6 Ω·cm.

11. The powder of the lithium transition-metal compound for a positive-electrode material in a lithium secondary battery according to claim 1 , wherein the powder is prepared by firing at 970° C. or higher in an oxygen-containing gas atmosphere.

12. The powder of the lithium transition-metal compound for a positive-electrode material in a lithium secondary battery according to claim 1 , wherein the carbon content C of the powder of the lithium transition-metal compound is in the range of 0.005% by weight to 0.05% by weight.

13. The powder of the lithium transition-metal compound for a positive-electrode material in a lithium secondary battery according to claim 1 , wherein in powder X-ray diffraction measurement using CuKα radiation, 0.01≦FWHM (110)≦0.2, where FWHM (110) represents the half-width of the (110) diffraction peak observed at a diffraction angle 2 θ of about 64.5°.

14. The powder of the lithium transition-metal compound for a positive-electrode material in a lithium secondary battery according to claim 1 , wherein in powder X-ray diffraction measurement using CuKα radiation, no diffraction peak from a heterophase is observed on the higher-angle side of the peak top of each of the (018) diffraction peak at a diffraction angle 2 θ of about 64° , the (110) diffraction peak at a diffraction angle 2 θ of about 64.5° , and the (113) diffraction peak at a diffraction angle 2 θ of about 68° , or in the case where a diffraction peak from a heterophase is observed, the ratio of the integrated intensity of the diffraction peak from the heterophase to the integrated intensity of a corresponding one of the diffraction peaks from a target crystal phase is within ranges described below:

0 ≦I 018* /I 018 ≦0.20,

0 ≦I 110* /I 110 ≦0.25, and

0 ≦I 113* /I 113 ≦0.30,

where I 018 represents the integrated intensity of the (018) diffraction peak, I 110 represents the integrated intensity of the (110) diffraction peak, I 113 represents the integrated intensity of the (113) diffraction peak, I 018 * represents the integrated intensity of the diffraction peak from the heterophase observed on the higher-angle side of the peak top of the (018) diffraction peak, I 110* represents the integrated intensity of the diffraction peak from the heterophase observed on the higher-angle side of the peak top of the (110) diffraction peak, and I 113* represents the integrated intensity of the diffraction peak from the heterophase observed on the higher-angle side of the peak top of the (113) diffraction peak.