Novel high-nickel ternary anode material and preparation
A positive electrode material and high-nickel technology, which is applied in the field of new high-nickel ternary positive electrode materials and their preparation, can solve the problems of difficult mining, low specific capacity, and increased material production costs, and achieve good thermal and electrochemical stability , Excellent cycle stability and rate performance, low degree of cation mixing
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0035] Example 1 The preparation of a novel high-nickel ternary positive electrode material comprises the following steps:
[0036] S1. Preparation of precursor by co-precipitation method: Weigh analytically pure nickel sulfate, cobalt sulfate, and manganese sulfate according to the stoichiometric ratio of the target sample and dissolve them in deionized water as a reaction feed solution for later use; take the corresponding amount of NaOH and dissolve them in deionized water As a precipitant for standby; use a four-necked flask as a reaction vessel, add a certain amount of deionized water into the four-necked flask as the reaction bottom liquid, seal the four-necked flask before the reaction starts, and pass argon gas into the bottle for a period of time , get rid of the oxygen in the reaction system; when the reaction starts, add an appropriate amount of ammonia water as a complexing agent in the bottom liquid, and add the reaction feed liquid and the precipitating agent (NaO...
Embodiment 2
[0039] Example 2 The preparation of a novel high-nickel ternary positive electrode material comprises the following steps:
[0040] S1. Preparation of precursor by co-precipitation method: Weigh analytically pure nickel sulfate, cobalt sulfate, and manganese sulfate according to the stoichiometric ratio of the target sample and dissolve them in deionized water as a reaction feed solution for later use; take the corresponding amount of NaOH and dissolve them in deionized water As a precipitant for standby; use a four-necked flask as a reaction vessel, add a certain amount of deionized water into the four-necked flask as the reaction bottom liquid, seal the four-necked flask before the reaction starts, and pass argon gas into the bottle for a period of time , get rid of the oxygen in the reaction system; when the reaction starts, add an appropriate amount of ammonia water as a complexing agent in the bottom liquid, and add the reaction feed liquid and the precipitating agent (NaO...
Embodiment 3
[0043] Example 3 The preparation of a novel high-nickel ternary positive electrode material comprises the following steps:
[0044] S1. Preparation of precursor by co-precipitation method: Weigh analytically pure nickel sulfate, cobalt sulfate, and manganese sulfate according to the stoichiometric ratio of the target sample and dissolve them in deionized water as a reaction feed solution for later use; take the corresponding amount of NaOH and dissolve them in deionized water As a precipitant for standby; use a four-necked flask as a reaction vessel, add a certain amount of deionized water into the four-necked flask as the reaction bottom liquid, seal the four-necked flask before the reaction starts, and pass argon gas into the bottle for a period of time , get rid of the oxygen in the reaction system; when the reaction starts, add an appropriate amount of ammonia water as a complexing agent in the bottom liquid, and add the reaction feed liquid and the precipitating agent (NaO...
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