A kind of synthetic method of nano manganese lithium stannate of novel lithium-ion battery cathode material
A technology for lithium-ion batteries and cathode materials, applied in battery electrodes, nanotechnology for materials and surface science, tin compounds, etc., can solve problems such as inability to mass-produce, achieve high equipment utilization, shorten transmission channels, The effect of easy process
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0029] (1) According to the element molar ratio Mn:Sn=1:1.5, weigh 49.02g of manganese acetate and add it to 300mL of deionized water to prepare a transparent solution. Weigh 80.02g of sodium stannate and add it to 100mL of deionized water to obtain a concentrated sodium stannate solution. The sodium stannate solution was added dropwise to the manganese acetate solution to form a precipitate. The precipitate was separated by suction filtration, washed with deionized water and absolute ethanol, and then baked in a vacuum drying oven at 120 °C for 12 h to obtain MnSn(OH) 6 precursor material;
[0030] (2) MnSn(OH) will be obtained 6 Precursor material in N 2 Atmosphere, calcination at 600℃ for 24h to obtain nano-MnSnO 3 Material;
[0031] (3) According to the molar ratio of MnSnO 3 : Li=1:1.2 Weigh 33.24g nanometer MnSnO 3 materials and 6.65g lithium carbonate, adding 60g ethanol as a dispersing medium, 0.4g PEG20000 as a dispersing agent, and preparing a uniform slurry wit...
Embodiment 2
[0035] (1) According to the element molar ratio Mn:Sn=1:1, weigh 30.20g of manganese sulfate and add it to 300mL of deionized water to prepare a transparent solution. Weigh 53.35g of sodium stannate and add it to 100mL of deionized water to obtain a concentrated sodium stannate solution. The sodium stannate solution was added dropwise to the manganese acetate solution to form a precipitate. The precipitate was separated by suction filtration, washed with deionized water and absolute ethanol, and then baked in a vacuum drying oven at 100 °C for 24 hours to obtain MnSn(OH) 6 precursor material;
[0036] ⑵ will get MnSn (OH )6 Precursor material in N 2 Atmosphere, calcination at 400℃ for 12h to obtain nano-MnSnO 3 Material;
[0037] (3) According to the molar ratio of MnSnO 3 : Li=1:1.2 Weigh 33.24g nanometer MnSnO 3Materials and 6.65g lithium carbonate, adding 27g ethylene glycol as a dispersing medium and 0.2g PEG4000 as a dispersing agent, prepared into a uniform slurry w...
Embodiment 3
[0041] (1) According to the element molar ratio Mn:Sn=1:1, weigh 49.02g of manganese acetate and add it to 300mL of deionized water to prepare a transparent solution. Weigh 53.35g of sodium stannate and add it to 100mL of deionized water to obtain a concentrated sodium stannate solution. The sodium stannate solution was added dropwise to the manganese acetate solution to form a precipitate. The precipitate was separated by suction filtration, washed with deionized water and absolute ethanol, and then baked in a vacuum drying oven at 100 °C for 12 h to obtain MnSn(OH) 6 precursor material;
[0042] (2) MnSn(OH) will be obtained 6 Precursor material in N 2 Atmosphere, calcination at 400℃ for 24h to obtain nano-MnSnO 3 Material;
[0043] (3) According to the molar ratio of MnSnO 3 : Li=1:1 Weigh 33.24g nanometer MnSnO 3 materials and 5.54g lithium carbonate, adding 27g ethanol as a dispersing medium, 0.4g PEG20000 as a dispersing agent, and preparing a uniform slurry with a ...
PUM
Property | Measurement | Unit |
---|---|---|
particle diameter | aaaaa | aaaaa |
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