Preparation method of carbon cloth based cathode iron oxide of lithium ion battery
A lithium-ion battery and carbon cloth-based technology, which is applied in the field of preparation of lithium-ion battery carbon cloth-based negative electrode iron oxide, can solve the problems of strong toxicity and sensitization, difficult waste liquid treatment, and high recycling costs, and achieve high Charge-discharge specific capacity, improve electrochemical activity and rate performance, and improve conductivity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0047] (1) Set the surface area to 30cm 2 The carbon cloth was ultrasonically cleaned in acetone, ethanol and ultrapure water for 40 minutes respectively, and after drying, it was immersed in 67% concentrated nitric acid and heated and stirred in a water bath at 60 ° C for 8 hours, cleaned with ultrapure water and dried .
[0048] (2) 1.3515 g of ferric chloride hexahydrate was dissolved in 49 milliliters of deionized water to prepare a ferric chloride solution with a concentration of 0.1 mol / L. The pretreated carbon cloth in step (1) was completely immersed in the above-mentioned ferric chloride solution, and heated in a water bath at 60° C. for 5 hours after ultrasonication for 15 minutes. The ultrasonic conditions are 40KHz, 20°C.
[0049] (3) The carbon cloth was taken out from the solution, rinsed with deionized water and dried at 80°C.
[0050] (4) Calcining the above-mentioned carbon cloth at 450° C. for 8 hours in air to obtain a carbon cloth-based negative electrod...
Embodiment 2
[0052] (1) Set the surface area to 100cm 2 The carbon cloth was ultrasonically cleaned in acetone, ethanol and ultrapure water for 40 minutes respectively, and after drying, it was immersed in 67% concentrated nitric acid and heated and stirred in a water bath at 120 ° C for 6 hours, cleaned with ultrapure water and dried .
[0053] (2) 1.3515 g of ferric chloride hexahydrate was dissolved in 49 milliliters of deionized water to prepare a ferric chloride solution with a concentration of 0.1 mol / L. The carbon cloth after the pretreatment in the step (1) is taken 90cm 2 Completely immerse in the above-mentioned ferric chloride solution, conduct ultrasonic heating reaction at 70° C. for 3 hours after ultrasonication for 15 minutes. The ultrasonic conditions are 40KHz, 25°C.
[0054] (3) The carbon cloth was taken out from the solution, rinsed with deionized water and dried at 80°C.
[0055] (4) Calcining the above-mentioned carbon cloth at 450° C. for 8 hours in the air to ob...
Embodiment 3
[0057] (1) Set the surface area to 300cm 2 The carbon cloth was ultrasonically cleaned in acetone, ethanol and ultrapure water for 40 minutes respectively, and after drying, it was immersed in 67% concentrated nitric acid and heated and stirred in a water bath at 120 ° C for 8 hours, cleaned with ultrapure water and dried .
[0058] (2) 1.3515 g of ferric chloride hexahydrate was dissolved in 49 milliliters of deionized water to prepare a ferric chloride solution with a concentration of 0.1 mol / L. The carbon cloth after the pretreatment in step (1) is taken 60cm 2 Completely immersed in the above-mentioned ferric chloride solution, ultrasonicated for 15 minutes, then heated in a water bath at 80°C for 4 hours. The ultrasonic conditions are 40KHz, 30°C.
[0059] (3) The carbon cloth was taken out from the solution, rinsed with deionized water and dried at 80°C.
[0060] (4) Calcining the above-mentioned carbon cloth at 450° C. for 8 hours in the air to obtain the carbon clo...
PUM
| Property | Measurement | Unit |
|---|---|---|
| diameter | aaaaa | aaaaa |
| diameter | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 


