Rapid preparation method of lithium ion battery positive electrode material vanadium pentoxide nanosheet
A technology of vanadium pentoxide nanometer and lithium ion battery, which is applied in the direction of vanadium oxide, battery electrode, nanotechnology for materials and surface science, etc. It can solve the problems of reducing the advantages of two-dimensional nanosheet structure and achieve good rate performance and cycle stability, shorten the diffusion transport path, and increase the effect of the contact area
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0030] (1) Add 0.6 g of commercial vanadium pentoxide and 1.9 g of citric acid into 20 mL of deionized water, stir at 80°C for 0.5 h to obtain a 0.33 mol / L vanadyl citrate solution; take 3 mL of vanadyl citrate solution and 0.032g of ammonium fluoride solid (the molar ratio of vanadyl citrate to ammonium fluoride is 1:0.88) was added to 30 mL of ethylene glycol solvent, stirred at room temperature for 0.5h, and then transferred to an autoclave for 200 React at ℃ for 12 hours. After natural cooling, solid-liquid separation, washing and drying with ethanol, dark green powder is obtained, which is the VO organic ligand precursor;
[0031] (2) The VO organic ligand precursor was heat-treated in the air at a rate of 4° / min to 400°C for 4 hours. After natural cooling, the product was collected to obtain a two-dimensional large-area V 2 o 5 Nanosheets.
[0032] (3) Preparation of lithium-ion battery electrode pole pieces for testing: the two-dimensional large-area V 2 o 5 Nano fl...
Embodiment 2
[0040] (1) Add 1.2 g of commercial vanadium pentoxide and 3.8 g of citric acid into 40 mL of deionized water, stir at 80°C for 0.5 h to obtain a 0.33 mol / L vanadyl citrate solution; take 6 mL of vanadyl citrate solution and 0.073g of ammonium fluoride solid (the molar ratio of vanadyl citrate and ammonium fluoride is 1:1) was added to 60 mL of ethylene glycol solvent, stirred at room temperature for 0.5h, then transferred to a high-pressure reactor for 200 React at ℃ for 12 hours. After natural cooling, solid-liquid separation, washing and drying with ethanol, dark green powder is obtained, which is the VO organic ligand precursor;
[0041] (2) Heat the VO organic ligand precursor in the air at a heating rate of 1 °C / min to 350 °C for 1 h. After natural cooling, collect the product to obtain a two-dimensional large-area V 2 o 5 Nanosheets.
[0042] (3) Preparation of lithium-ion battery electrode pole pieces for testing: the two-dimensional large-area V 2 o 5 Nano flake ac...
Embodiment 3
[0046] (1) Add 2.4 g of commercial vanadium pentoxide and 7.6 g of citric acid into 80 mL of deionized water, stir at 80°C for 0.5 h to obtain a 0.33 mol / L vanadyl citrate solution; take 12 mL of vanadyl citrate solution and 0.146g of ammonium fluoride solid (the molar ratio of vanadyl citrate and ammonium fluoride is 1:1) was added to 120 mL of ethylene glycol solvent, stirred at room temperature for 0.5h, and then transferred to an autoclave for 200 React at ℃ for 12 hours. After natural cooling, solid-liquid separation, washing and drying with ethanol, dark green powder is obtained, which is the VO organic ligand precursor;
[0047] (2) The VO organic ligand precursor was heat-treated in air at a rate of 4°C / min to 400°C for 4 hours. After natural cooling, the product was collected to obtain a two-dimensional large-area V 2 o 5 Nanosheets.
[0048] (3) Preparation of lithium-ion battery electrode pole pieces for testing: the two-dimensional large-area V 2 o 5 Nano flake...
PUM
| Property | Measurement | Unit |
|---|---|---|
| thickness | aaaaa | aaaaa |
| size | aaaaa | aaaaa |
| thickness | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 


