Modified positive electrode material and preparation method thereof and secondary battery
A positive electrode material and modification technology, applied to battery electrodes, circuits, electrical components, etc., can solve problems such as reducing the capacity and energy density of single batteries, affecting the cycle life of fast-charging batteries, and reducing the first Coulombic efficiency. Effects on Structural Stability and Dynamic Properties
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0022] According to the preparation method of the modified positive electrode material described in the second aspect of the present invention, it is used to prepare the modified positive electrode material described in the first aspect of the present invention, comprising the steps of: (1) combining Ma source, Mo source and P source by atoms The ratio Ma:Mo:P=x:y:z is uniformly mixed and processed to obtain Ma with a NASICON-like crystal structure x Mo y P z o n ; (2) will get Ma x Mo y P z o n After being uniformly mixed with the positive active material, calcining is carried out to obtain a coating layer Ma on the surface of the positive active material. x Mo y P z o n modified cathode materials. Wherein, Ma is selected from Li or Na, x is an integer within 1 to 3, and y, z, n are integers greater than 0.
[0023] In the preparation method of the modified cathode material according to the second aspect of the present invention, the Ma source is selected from one ...
Embodiment 1
[0044] (1) Mo source MoO 3 After mixing with oxalic acid and stirring evenly (MoO 3 The molar ratio to oxalic acid is 1:3~1:4) dissolved in deionized water at 75°C, and then added P source NH 4 h 2 PO 4 with Ma Yuan Li 2 CO 3 , and control the molar ratio of Li, Mo, P to 3:4:5. Then the mixed solution was stirred for 4 hours and then heated in an oven at 100 °C, dried with deionized water to prepare a gel, and then sintered at 650 °C for 6 hours to obtain Li 3 Mo 4 P 5 o 24 . Will Li 3 Mo 4 P 5 o 24 Grind and sieve to ensure that the particle size of the particles is within 10 μm.
[0045] (2) The sieved Li 3 Mo 4 P 5 o 24 and positive active material LiNi 0.3 co 0.2 mn 0.5 o 2 According to the mass ratio of 0.5:100 solid-phase ball milling and mixing, and then calcining the mixed powder at 450 ° C for 3 hours, the modified positive electrode material is obtained, and the modified positive electrode material obtained after calcining is sieved, and the par...
Embodiment 2
[0047] (1) Mo source H 2 MoO 4 After mixing with oxalic acid and stirring evenly (H 2 MoO 4 The molar ratio to oxalic acid is 1:3~1:4) dissolved in deionized water at 75°C, and then added P source NH 4 h 2 PO 4 with Ma Yuan Li 2 CO 3 , and control the molar ratio of Li, Mo, P to 3:4:5. Then, the mixed solution was stirred for 4 hours and then heated in an oven at 100°C, dried with deionized water to prepare a gel, and then sintered at 700°C for 6 hours to obtain Li 3 Mo 4 P 5 o 24 . Will Li 3 Mo 4 P 5 o 24 Grind and sieve to ensure that the particle size of the particles is within 15 μm.
[0048] (2) The sieved Li 3 Mo 4 P 5 o 24 and positive active material LiNi 0.3 co 0.3 mn 0.4 o 2 According to the mass ratio of 1:100, solid-phase ball milling and mixing, and then calcining the mixed powder at 480°C for 3.5h, the modified positive electrode material is obtained, and the modified positive electrode material obtained after calcining is sieved, and the pa...
PUM
| Property | Measurement | Unit |
|---|---|---|
| Particle size | aaaaa | aaaaa |
| Particle size | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 

