# US 10,122,013 B2 · Cathode active material and process for its production

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- Number: US 10,122,013 B2
- Document ID: US10122013B2
- Status: Granted
- Kind: B2
- Application number: 14/663,033
- Filed: 2015-03-19
- Published: 2015-07-16
- Granted: 2018-11-06
- Earliest claimed: 2012-10-29
- Assignees: Sumitomo Chemical Company, Limited
- Applicants: Sumitomo Chemical Co., Ltd.
- Inventors: Tomohiro Sakai; Kentaro Tsunozaki; Michinori Suehara
- Web page: https://patentgrep.com/patent/US10122013B2

## CPC

- H01M 4/505: of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
- H01M 4/0471: {involving thermal treatment, e.g. firing, sintering, backing particulate active material, thermal decomposition, pyrolysis}
- H01M 4/0497: {Chemical precipitation}
- H01M 4/525: of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
- H01M 10/052: Li-accumulators
- H01M 2004/028: {Positive electrodes}
- Y02E 60/10: Energy storage using batteries
- H01M: PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- Y02E: REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION

## Abstract

To provide a cathode active material having excellent cycle characteristics and a small decrease in the discharge voltage, and a process for its production. A process for producing a cathode active material, which comprises a step of mixing at least one sulfate (A) selected from the group consisting of a sulfate of Ni, a sulfate of Co and a sulfate of Mn with at least one carbonate (B) selected from the group consisting of sodium carbonate and potassium carbonate in an aqueous solution state to obtain a coprecipitated compound, a step of mixing the coprecipitated compound with an aqueous phosphate solution, a step of volatilizing a water content from the mixture of the coprecipitated compound and the aqueous phosphate solution to obtain a precursor compound, and a step of mixing the precursor compound with lithium carbonate and firing the mixture at from 500 to 1000° C.; and a cathode active material obtainable by the production process, which comprises Li, at least one transition metal element (X) selected from the group consisting of Ni, Co and Mn, and P, wherein the average coefficient of variation (CV value) of the calculated peak intensity ratio (Ip/Ix) of P to the transition metal element (X) is from 0 to 20% as determined by a method for measuring coefficient of variation.

## Claims

### Claim 1

A cathode active material, comprising:
Li;
P; and
at least one transition metal element (X) selected from the group consisting of Ni, Co, and Mn;
wherein the material satisfies formula (1):
Li1+aPbNicCodMneO2+f (1)
wherein 0.1≤a≤0.6, 0.001≤b≤0.1, 0.1≤c≤0.5, 0≤d≤0.3, 0.2≤e≤0.9, 0.9≤c+d+e≤1.05, and f is a value determined from the valences of Li, P, Ni, Co, and Mn
wherein:
an average coefficient of variation (CV value) of a calculated peak intensity ratio (Ip/Ix) of P to the transition metal element (X) is from 0 to 20%; and
the average CV value is determined by:
scanning a cross section of each of three samples of the cathode active material with an electron probe microanalyzer at 2 μm intervals in a diameter direction with a spot diameter of 2 μm to measure a calculated peak intensity (Ip) of P and a calculated peak intensity (Ix) of the transition metal element (X) and determine the calculated peak intensity ratio (Ip/Ix) of P to the transition metal element (X) at each measurement spot;
determining CV values of the calculated peak intensity ratio (Ip/Ix) for each sample; and
determining the average CV value of the samples.

### Claim 2 (depends on 1)

A process for producing the cathode active material according to claim 1, which comprises the following steps (I) to (IV):
(I) a step of mixing at least one sulfate (A) selected from the group consisting of a sulfate of Ni, a sulfate of Co and a sulfate of Mn, with at least one carbonate (B) selected from the group consisting of sodium carbonate and potassium carbonate in an aqueous solution state to obtain a coprecipitated compound containing at least one transition metal element (X) selected from the group consisting of Ni, Co and Mn;
(II) a step of mixing the coprecipitated compound with an aqueous phosphate solution;
(III) a step of volatilizing a water content from the mixture of the coprecipitated compound and the aqueous phosphate solution to obtain a precursor compound; and
(IV) a step of mixing the precursor compound with lithium carbonate and firing the mixture at from 500 to 1000° C.

### Claim 3 (depends on 2)

The process for producing a cathode active material according to claim 2, wherein in the step (I), the concentration of the transition metal element (X) in the aqueous solution of the sulfate (A) is from 0.1 to 3 mol/kg, and the concentration of the carbonate (B) in the aqueous solution of the carbonate (B) is from 0.1 to 2 mol/kg.

### Claim 4 (depends on 2)

The process for producing a cathode active material according to claim 2, wherein in the step (I), the pH of the solution mixture is from 7 to 12 when the aqueous solution of the sulfate (A) and the aqueous solution of the carbonate (B) are mixed.

### Claim 5 (depends on 2)

The process for producing a cathode active material according to claim 2, wherein the coprecipitated compound in the step (I) is a carbonate containing Ni, Co and Mn.

### Claim 6 (depends on 2)

The process for producing a cathode active material according to claim 2, wherein in the step (II), mixing of the coprecipitated compound and the aqueous phosphate solution is carried out by a spray coating method.

### Claim 7 (depends on 2)

The process for producing a cathode active material according to claim 2, wherein the aqueous phosphate solution in the step (II) and the step (III) is an aqueous solution of at least one member selected from the group consisting of phosphoric acid, ammonium dihydrogen phosphate and diammonium hydrogen phosphate.

### Claim 8 (depends on 2)

The process for producing a cathode active material according to claim 2, wherein in the step (II), the ratio (P/X) of the total number of moles of P contained in the phosphate to the total number of moles of the transition metal element (X) contained in the coprecipitated compound is from 0.01 to 10 mol%.

### Claim 9 (depends on 2)

The process for producing a cathode active material according to claim 2, wherein in the step (IV), the ratio (Li/X) of the total number of moles of Li contained in the lithium carbonate to the total number of moles of the transition metal element (X) contained in the precursor compound is at least 1.1 times.

### Claim 10 (depends on 1)

The cathode active material according to claim 1, wherein an average of the calculated peak intensity ratios (Ip/Ix) of each sample is from 0.001 to 0.1.

### Claim 11 (depends on 1)

The cathode active material according to claim 1, wherein:
a ratio (Li/X) of a number of moles of Li to a number of moles of the transition metal element (X) is at least 1.1 times; and
a ratio (P/X) of a number of moles of P to the number of moles of the transition metal element (X) is from 0.01 to 10 mol%.

### Claim 12 (depends on 1)

A cathode for a lithium ion secondary battery, comprising a cathode current collector and a cathode active material layer formed on the cathode current collector;
wherein the cathode active material layer comprises the cathode active material as defined in claim 1, an electrically conductive material, and a binder.

### Claim 13 (depends on 12)

A lithium ion secondary battery, comprising the cathode for a lithium ion secondary battery according to claim 12, an anode, and a non-aqueous electrolyte.

### Claim 14 (depends on 1)

The cathode active material according to claim 1, wherein the transition metal element (X) comprises Co.