Square lithium ion power battery and preparation method thereof
A power battery and lithium-ion technology, which is applied in the field of square lithium-ion power batteries and their preparation, can solve the problems of poor charge and discharge characteristics, cycle performance and safety performance, and achieve improved high-power charge and discharge characteristics, improved arrangement structure, Good safety and reliability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example 1
[0038] 1) Preparation of positive electrode active material: The raw material LiNO 3 , Mn(CH 3 COO) 2 4H 2 O, Ni(CH 3 COO) 2 ·6H 2 O and Co(CH 3 COO) 2 4H 2 O is dissolved in absolute ethanol (an excess of 3% lithium salt is added to offset the loss of lithium at high temperature) to form a metal salt ethanol solution, and the lithium salt, nickel salt, manganese salt and cobalt salt in the metal salt ethanol solution The total concentration is 1mol / L.
[0039] Take 10mL metal salt ethanol solution and put it into a 100mL corundum crucible, put the corundum crucible into a box furnace preheated to 500°C, ignite, react vigorously in the air for 10 minutes, cool to room temperature 25°C, and obtain the preliminary The product, after grinding the preliminary product, put it into the box furnace again, annealed it at a high temperature of 800°C for 16 hours, and then cooled it to room temperature 25°C with the furnace to obtain the positive electrode active material.
[...
preparation example 2
[0043] 1) Preparation of positive electrode active material: The raw material LiNO 3 , Mn(NO 3 ) 2 ·6H 2 O, Ni(NO 3 ) 2 ·6H 2 O and Co(CH 3 COO) 2 4H 2 O is dissolved in absolute ethanol (an excess of 3% lithium salt is added to offset the loss of lithium at high temperature) to form a metal salt ethanol solution, and the lithium salt, nickel salt, manganese salt and cobalt salt in the metal salt ethanol solution The total concentration is 2mol / L.
[0044]Take 10mL metal salt ethanol solution and put it into a 100mL corundum crucible, put the corundum crucible into a box furnace preheated to 500°C, ignite, react vigorously in the air for 10 minutes, cool to room temperature 25°C, and obtain the preliminary The product, after grinding the preliminary product, put it into the box furnace again, annealed it at a high temperature of 800°C for 16 hours, and then cooled it to room temperature 25°C with the furnace to obtain the positive electrode active material.
[0045] ...
preparation example 3
[0048] The preparation of the negative electrode plate with the negative active material coating on one side left uncoated: Weigh 93% modified natural graphite (Shenzhen Bestray Electronic Materials Co., Ltd., model CG-8), 3% conductive agent (Cabot50 conductive carbon black) and 4% water-based binder (the volume ratio of sodium carboxymethyl cellulose: styrene-butadiene rubber (SBR-1500) is 1:1), to obtain a mixture, adding relative to the mixing After vacuum stirring with 60% deionized water of the weight of the material, it is continuously double-sided coated on the copper foil and left on the same side of the same side of the copper foil, and the part that is not coated with the negative electrode active material coating is left on one side, and dried Continuous roll pressing after deionized water; after slitting, a negative electrode plate with an uncoated negative electrode active material coating on one side remains.
PUM
Property | Measurement | Unit |
---|---|---|
length | aaaaa | aaaaa |
width | aaaaa | aaaaa |
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