Lithium iron phosphate modified material, preparation method and lithium battery using modified material
A technology of lithium iron phosphate and modified materials, applied in battery electrodes, secondary batteries, circuits, etc., can solve the problems of poor rate performance and cycle life
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0023] The present invention provides a kind of preparation method of lithium iron phosphate modified material, wherein, this preparation method comprises:
[0024] (1) first mixing and drying the first lithium source, the first iron source, the first phosphorus source and the solvent to obtain solid particles;
[0025] (2) Oxidize the solid particles to obtain a first precursor, which contains Li 3 Fe 2 (PO 4 ) 3 and Fe 2 o 3 ;
[0026] (3) The second lithium source, the second iron source, the manganese source, the second phosphorus source and the solvent are mixed for the second time;
[0027] (4) The first precursor and the second mixed product are mixed for the third time, and then the third mixed product is mixed with the carbon source for the fourth time to obtain the second precursor;
[0028] (5) Calcining the second precursor in a protective atmosphere to obtain a lithium iron phosphate modified material containing lithium iron phosphate, lithium iron manganes...
Embodiment 1
[0056] This example is used to illustrate the lithium iron phosphate composite material and its preparation method of the present invention.
[0057] (1) 150.82g FePO 4 , 36.95g Li 2 CO 3 and 200g of distilled water were placed in a ball mill for wet ball milling for 2 hours at a speed of 600r / min; the product after ball milling was spray-dried with an inlet temperature of 200°C and an outlet temperature of 90°C; The diameter is 1 μm;
[0058] (2) The product obtained in step (1) is oxidized at 450°C for 4 hours in an air atmosphere to obtain the first precursor, which contains Fe enriched on the surface 2 o 3 Li 3 Fe 2 (PO 4 ) 3 Solid particles; mix and disperse the first precursor and 180g distilled water to form suspension A;
[0059] (3) 3.91g Fe 2 o 3 , 4.58g Mn 3 o 4 , 10.39gLiH 2 PO 4 and 19g of distilled water were sequentially added into a ball mill tank for wet ball milling for 2 hours, and the rotating speed of the ball mill was 600r / min to form a sus...
Embodiment 2
[0065] (1) 150.82g FePO 4 , 41.96gLiOH·H 2 0 and 290g distilled water are placed in ball mill and carry out wet ball milling 2.5h, and the rotating speed of ball milling is 700r / min; The product after ball milling is carried out spray drying, and inlet temperature is 240 ℃, and outlet temperature is 95 ℃; Spray drying forms spherical product, The average particle size is 1.2μm;
[0066] (2) The product obtained in step (1) was oxidized at 420°C for 6 hours in an air atmosphere to obtain the first precursor, which contained Fe enriched on the surface 2 o 3 Li 3 Fe 2 (PO 4 ) 3 Solid particles; mix and disperse the first precursor and 200g distilled water to form suspension A;
[0067] (3) 4.83g FePO 4 , 5.52g MnCO 3 , 4.99gLiH 2 PO 4 , 1.34gLiOH·H 2 0 and 17g of water were sequentially added into a ball mill tank for wet ball milling for 2 hours, and the rotating speed of the ball mill was 700r / min to form a suspension B;
[0068] (4-1) After uniformly mixing suspen...
PUM
| Property | Measurement | Unit |
|---|---|---|
| The average particle size | aaaaa | aaaaa |
| Specific capacity | aaaaa | aaaaa |
| Discharge specific capacity | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More - R&D
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com



