Lithium ion battery negative nanometer material SnO2/MCMB (Mesophase Carbon Micro Beads) shell, and preparation method and application thereof
A lithium ion battery and nanomaterial technology, which is applied in the field of lithium ion battery negative electrode nanomaterial SnO2/MCMB core-shell and its preparation, can solve the problems of cycle performance degradation, internal structure change, reduction of specific capacity, etc., and achieves improved cycle performance, The effect of improving performance and simple preparation process
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0057] (1) Mix 25mL of 98wt% concentrated sulfuric acid and 75mL of 60wt% concentrated nitric acid to obtain a mixed acid; disperse 2g of MCMB (5-12 microns) in the mixed acid, reflux at 50°C for 10h, then add 10mL of 35wt% H 2 o 2 , continue to stir for 5 hours, then centrifuge three times with deionized water and ethanol, collect the precipitate, and dry it in vacuum at 80°C for 5 hours to obtain pretreated MCMB;
[0058] (2) Ultrasonic disperse 0.5 g of pretreated MCMB from step (1) in 100 mL of deionized water, and take 5.21 g of SnCl 4 As a tin source, make the molar concentration ratio of tin atoms 0.2mol / L, add 25wt% ammonia water dropwise until the pH of the solution is 7, stir for 2h, centrifuge three times with deionized water and ethanol successively, collect the precipitate, and vacuum dry at 90°C 8h, get Pre-MCMB-SnO 2 ;
[0059] (3) Add 0.6g of Pre-MCMB-SnO from step (2) 2 , 2.13g sodium stannate and 0.32g sodium hydroxide are added to 40mL mixed solution (de...
Embodiment 2
[0063] (1) Mix 25mL of 98wt% concentrated sulfuric acid and 75mL of 60wt% concentrated nitric acid to obtain a mixed acid; disperse 2g of MCMB (5-12 microns) in the mixed acid, reflux at 50°C for 11h, and then add 15mL of 30wt% H 2 o 2 , continue to stir for 5 hours, then centrifuge three times with deionized water and ethanol, collect the precipitate, and dry it in vacuum at 80°C for 5 hours to obtain pretreated MCMB;
[0064] (2) Ultrasonic disperse 0.5 g of pretreated MCMB from step (1) in 100 mL of deionized water, and take 6.51 g of SnCl 4 As a tin source, make the molar concentration ratio of tin atoms 0.25mol / L, add 30wt% ammonia water dropwise until the pH of the solution is 8, stir for 2h, centrifuge three times with deionized water and ethanol successively, collect the precipitate, and dry it under vacuum at 80°C 12h, get Pre-MCMB-SnO 2 ;
[0065] (3) Add 0.6g of Pre-MCMB-SnO from step (2) 2 , 2.66g sodium stannate and 0.48g sodium hydroxide are added to 40mL mix...
Embodiment 3
[0069] (1) Mix 25mL of 98wt% concentrated sulfuric acid and 75mL of 60wt% concentrated nitric acid to obtain a mixed acid; disperse 2g of MCMB (5-12 microns) in the mixed acid, reflux at 50°C for 12h, then add 20mL of 32wt% H 2 o 2 , continue to stir for 5 hours, then centrifuge three times with deionized water and ethanol, collect the precipitate, and dry it in vacuum at 80°C for 5 hours to obtain pretreated MCMB;
[0070] (2) Ultrasonic disperse 0.5 g of pretreated MCMB from step (1) in 100 mL of deionized water, and take 7.81 g of SnCl 4 As a tin source, make the molar concentration ratio of tin atoms 0.3mol / L, add 35wt% ammonia water dropwise until the pH of the solution is 8, stir for 2h, centrifuge three times with deionized water and ethanol successively, collect the precipitate, and dry it under vacuum at 60°C 24h, get Pre-MCMB-SnO 2 ;
[0071] (3) Add 0.6g of Pre-MCMB-SnO from step (2) 2 , 3.2g sodium stannate and 0.64g sodium hydroxide are added to 40mL mixed sol...
PUM
Property | Measurement | Unit |
---|---|---|
thickness | 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