A kind of nickel cobalt lithium manganate cathode material and preparation method thereof
A technology of nickel cobalt lithium manganate and positive electrode material, which is applied in the field of positive electrode material and its preparation, can solve the problems of low stability of structure and composition electrochemical performance, slow solid-phase diffusion, difficult to mix uniformly, etc., and achieves excellent performance. Rate and cycle performance, uniform distribution, good crystallization effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0034] Prepare nickel cobalt lithium manganese oxide cathode material according to the following steps:
[0035] (1) Weigh 2kg of nickel-cobalt-manganese hydroxide, 1.1kg of lithium hydroxide monohydrate, and 3kg of deionized water into a 10L autoclave;
[0036] (2) Turn on the stirring, keep the stirring speed at 60 rpm, and the reaction temperature is 50°C, at 10m 3 Ozone with a concentration of 60mg / L is introduced at a flow rate of / h to cause the nickel-cobalt-manganese hydroxide to undergo an oxidation reaction, and the reaction time is 2h;
[0037] (3) Raise the reaction temperature of the autoclave to 200°C, control the pressure inside the autoclave at 3.0MPa, react for 1h, and form nickel-cobalt-lithium manganate precipitate, and cool to 40-50°C;
[0038] (4) Pour the nickel-cobalt-lithium-manganese oxide precipitate into a centrifuge for filtration, put the filtered material into a muffle furnace for sintering, the sintering temperature is 800°C, the sintering time ...
Embodiment 2
[0048] Prepare nickel cobalt lithium manganese oxide cathode material according to the following steps:
[0049] (1) Weigh 2kg of nickel-cobalt-manganese hydroxide, 1.1kg of lithium hydroxide monohydrate, and 3kg of deionized water into a 10L autoclave;
[0050] (2) Turn on the stirring, keep the stirring speed at 60 rpm, and the reaction temperature is 50°C, at 10m 3 Ozone with a concentration of 80mg / L is introduced at a flow rate of / h to make the nickel-cobalt-manganese hydroxide oxidize, and the reaction time is 2h;
[0051] (3) Raise the reaction temperature of the autoclave to 250 °C, control the pressure inside the autoclave at 5.0 MPa, react for 1 hour, and form nickel-cobalt lithium manganate precipitate, and cool to 40-50 °C;
[0052] (4) Pour the nickel-cobalt-lithium-manganese-oxide precipitation into a centrifuge to filter, put the filtered material into a muffle furnace for sintering, the sintering temperature is 850°C, the sintering time is 8h, and the sintere...
Embodiment 3
[0076] Prepare nickel cobalt lithium manganese oxide cathode material according to the following steps:
[0077] (1) Weigh 2kg of nickel-cobalt-manganese hydroxide, 0.5kg of lithium hydroxide monohydrate, and 2kg of deionized water into a 10L autoclave;
[0078] (2) Turn on the stirring, keep the stirring speed at 60 rpm, and the reaction temperature is 40°C, 3 Ozone with a concentration of 100mg / L is introduced at a flow rate of / h to cause the nickel-cobalt-manganese hydroxide to undergo an oxidation reaction, and the reaction time is 10h;
[0079] (3) Raise the reaction temperature of the autoclave to 150°C, control the pressure inside the autoclave at 0.2MPa, react for 5h, and form nickel-cobalt-lithium-manganate precipitate, and cool to 40-50°C;
[0080] (4) Pour the nickel-cobalt-lithium-manganese-oxide precipitate into a centrifuge for filtration, put the filtered material into a muffle furnace for sintering, the sintering temperature is 600°C, the sintering time is 15...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com