Preparation method of monovalent ion-doped spinel rich-lithium lithium manganate anode material
A technology of lithium-rich lithium manganese oxide and positive electrode materials, applied in battery electrodes, electrical components, circuits, etc., can solve the problems of cycle performance attenuation, poor discharge performance, and unstable structure, and achieve low raw material cost, good cycle performance, The effect of the simple preparation process
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0036] Weigh lithium hydroxide, manganese acetate and sodium hydroxide respectively according to the molar ratio of lithium ion, manganese ion and sodium ion at 1: 1.15: 0.10. Mix the weighed lithium hydroxide, manganese acetate, and sodium hydroxide, add ethanol 10 times the volume of the total solid volume, and use a super energy ball mill for wet grinding and mixing for 8 hours to prepare precursor 1. Precursor 1 was dried at 160° C. and a pressure of 1000 Pa to prepare Precursor 2 . Precursor 2 was placed in an oxygen-enriched air atmosphere with an oxygen volume content of 52%, sintered at 180°C for 9 hours, then heated from 180°C to 510°C at a heating rate of 5°C / min, and kept at the temperature for sintering for 19 hours to prepare a tip. Spar lithium-rich lithium manganese oxide cathode material.
[0037] Compared with other inventive methods, the present invention has lower cost of raw materials, wide sources of raw materials, simple preparation process, good dischar...
Embodiment 2
[0039] Weigh lithium carbonate, manganese monoxide, and sodium oxide respectively according to the molar ratio of lithium ions, manganese ions, and dopant ions being 0.95: 1.05: 0.15. Mix the weighed lithium carbonate, manganese monoxide, and sodium oxide, add deionized water that is 1 times the volume of the total solid volume, and use a super energy ball mill for wet grinding and mixing for 3 hours to prepare precursor 1. Precursor 1 was vacuum-dried at 80° C. and 10 Pa pressure to prepare Precursor 2 . Precursor 2 was placed in an oxygen-enriched air atmosphere with an oxygen volume content of 22%, sintered at 150°C for 3 hours, then heated from 150°C to 400°C at a heating rate of 1°C / min, and kept at the temperature for sintering for 3 hours to prepare the tip. Spar lithium-rich lithium manganese oxide cathode material.
[0040] Compared with other inventive methods, the invention has lower cost of raw materials, wide sources of raw materials, simple preparation process, ...
Embodiment 3
[0042]Weigh lithium citrate, manganese acetate, and sodium citrate respectively according to the molar ratio of lithium ions, manganese ions, and sodium ions at 1.06: 1.20: 0.02. Mix the weighed lithium citrate, manganese acetate, and sodium citrate, add formaldehyde 15 times the volume of the total solid volume, and wet grind and mix for 15 hours with a wet mill to prepare precursor 1. Precursor 1 was vacuum-dried at 280° C. and 10132 Pa to prepare Precursor 2 . Precursor 2 was placed in an oxygen-enriched air atmosphere with an oxygen volume content of 99%, sintered at 300°C for 15 hours, then heated from 300°C to 600°C at a heating rate of 30°C / min, and kept at the temperature for sintering for 24 hours to prepare the tip. Spar lithium-rich lithium manganese oxide cathode material.
[0043] Compared with other inventive methods, the invention has lower cost of raw materials, wide sources of raw materials, simple preparation process, good discharge performance under high cu...
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