Lithium-rich manganese-based positive electrode material and preparation method and application thereof
A cathode material, lithium-rich manganese-based technology, applied in the field of lithium-rich manganese-based cathode materials and its preparation, can solve the problems of capacity fading, low initial efficiency, etc., and achieve the effect of improved cycle performance, high specific capacity, and good rate performance
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0067] (1) Weigh 1mol of Mn 0.6 Ni 0.2 co 0.2 CO 3 and transferred to a mortar and ground until the D50 particle size is not greater than 8 μm, and the ground precursor material is subjected to the first calcination treatment in an oxygen atmosphere furnace at 500°C to obtain the first calcination product, wherein the calcination time is 8h, oxygen The concentration is 20v%; (2) the first calcined product is mixed with 1.55mol of LiOH·H 2 O mixed and ground for 1 h, and then the second calcination treatment was carried out in an oxygen atmosphere furnace at 800 ° C to obtain the positive electrode preparation material 0.5 Li 2 MnO 3 -0.5LiMn 0.6 Ni 0.2 co 0.2 o 2 , wherein the time of the second calcination treatment is 12h, the oxygen concentration is 20v%, and the D50 particle diameter of the first calcination product and the lithium salt after grinding is not more than 8 μm; (3) Weigh 5g of the positive electrode preparation material and add a concentration of 0.1m...
Embodiment 2
[0069] (1) Weigh 1mol of Mn 0.6 Ni 0.2 co 0.2 CO 3 and transferred to a mortar and ground until the D50 particle size is not greater than 8 μm, and the ground precursor material is subjected to the first calcination treatment in an oxygen atmosphere furnace at 500°C to obtain the first calcination product, wherein the calcination time is 8h, oxygen The concentration is 20v%; (2) the first calcined product is mixed with 1.5mol of LiOH·H 2 O mixed and ground for 1 h, and then the second calcination treatment was carried out in an oxygen atmosphere furnace at 800 ° C to obtain a positive electrode preparation material of 0.45 Li 2 MnO 3 -0.55LiMn 0.6 Ni 0.2 co 0.2 o 2 , wherein the time of the second calcination treatment is 12h, the oxygen concentration is 20v%, and the D50 particle diameter of the first calcination product and the lithium salt after grinding is not more than 8 μm; (3) Weigh 5g of the positive electrode preparation material and add a concentration of 0....
Embodiment 3
[0071] (1) Weigh 1mol of Mn 0.6 Ni 0.2 co 0.2 CO 3 and transferred to a mortar and ground until the D50 particle size is not greater than 8 μm, and the ground precursor material is subjected to the first calcination treatment in an oxygen atmosphere furnace at 500°C to obtain the first calcination product, wherein the calcination time is 8h, oxygen The concentration is 20v%; (2) the first calcined product is mixed with 1.6mol of LiOH·H 2 O mixed and ground for 1 h, and then the second calcination treatment was carried out in an oxygen atmosphere furnace at 800 ° C to obtain the positive electrode preparation material 0.55 Li 2 MnO 3 -0.45LiMn 0.6 Ni 0.2 co 0.2 o 2 , wherein the time of the second calcination treatment is 12h, the oxygen concentration is 20v%, and the D50 particle diameter of the first calcination product and the lithium salt after grinding is not more than 8 μm; (3) Weigh 5g of the positive electrode preparation material and add a concentration of 0.1...
PUM
| Property | Measurement | Unit |
|---|---|---|
| particle diameter | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More - R&D
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com



