Cathode active material, method for preparing same, and lithium secondary battery comprising same
By using lithium transition metal oxide particles and specific composite particles in the cathode active material of lithium secondary batteries to form a coating layer or internal doping, the problems of cracking and shortening of the lifespan of the cathode active material of lithium secondary batteries are solved and achieved Higher structural stability and battery cycle performance.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
preparation example Construction
[0080] The preparation method of the positive electrode active material according to an embodiment of the present invention may include the steps of mixing and heat-treating lithium transition metal oxide particles and composite particles. (La (1-x) Sr x MnO 3 ), CSZ, SSZ, and Ni-YSZ, or a mixture of two or more of them.
[0081] Preferably, according to an embodiment of the present invention, the above-mentioned composite particles include one or a mixture of two or more selected from the group consisting of YSZ, CSZ and SSZ.
[0082] According to an embodiment of the present invention, the above heat treatment may be performed at a temperature range of 100° C. to 1200° C. for 4 hours to 24 hours.
[0083] According to a method for preparing a positive electrode active material according to an embodiment of the present invention, a coating layer is formed on the surface of the lithium transition metal oxide particles or the composite particles are contained in the lithium ...
Embodiment
[0123] Hereinafter, the present invention will be further described with examples and experimental examples, but the present invention is not limited by these examples and experimental examples.
[0124]
preparation example 1
[0126] 55.84g of LiOH (H 2 O), the average particle diameter of 123.61g is the Ni of 12 μ m 0.6 mn 0.2 co 0.2 (OH) 2 The experimental stirrer was placed, and mixing was performed for 1 minute so that the rotational speed of the central part of the experimental stirrer was 18000 rpm.
[0127]The obtained above-mentioned precursor was put into a 500 cc aluminum crucible, and calcined at a temperature of about 900° C. and an air (Air) atmosphere for 6 hours. The cake obtained after calcination was pulverized, and then classified using a 400-mesh sieve (manufactured by Taylor Standard Sieve in the United States) to obtain LiNi 0.6 mn 0.2 co 0.2 o 2 .
[0128]
PUM
| Property | Measurement | Unit |
|---|---|---|
| compressive strength | aaaaa | aaaaa |
| particle diameter | aaaaa | aaaaa |
| particle diameter | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 