Preparation method of non-stoichiometry ruthenium dioxide electrode material
A non-stoichiometric, ruthenium dioxide technology, applied in hybrid capacitor electrodes, hybrid/electric double-layer capacitor manufacturing, etc., can solve the problem of lack of electrochemical activity, affect the quality of tantalum ruthenium capacitor products, and limit the high specific capacity of ruthenium dioxide and other issues to achieve the effect of high specific capacitance
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0013] Dissolve 10g of commercially available industrially pure ruthenium trichloride in 150ml of deionized water, add 5ml of anhydrous low-molecular alcohol (methanol) and fuming hydrochloric acid respectively during the dissolution process, stir vigorously for 30 minutes, and continue stirring after completely dissolving Next, add deionized water continuously, and continue to stir until the pH value of the solution reaches 4.5. Ammonium bicarbonate with a concentration of 0.5M was added to the reaction system by spraying. While continuing to stir the reaction liquid, add 5ml of perchloric acid into the system by spraying, keep stirring the reaction liquid for 30 minutes, let it stand, age for 10 hours, wash with water under reduced pressure and filter for 3 times to obtain a filter cake. The filter cake is blast-dried at 60°C for 6 hours and crushed into fine particles, then placed in a muffle furnace for sintering for 8 hours at a sintering temperature of 175°C, dried at 80...
Embodiment 2
[0015] Dissolve 20g of commercially available commercially pure ruthenium trichloride in 150ml of deionized water, add 8ml of anhydrous low-molecular alcohol (ethylene glycol) and fuming hydrochloric acid respectively during the dissolution process, stir vigorously for 30 minutes, and continue stirring after completely dissolving In the case of continuous addition of deionized water, and continue stirring until the pH value of the solution reaches 5.3. Sodium bicarbonate with a concentration of 0.5M was added to the reaction system by spraying. In the case of continuing to stir the reaction liquid, the reaction system was passed into ozone for 60 minutes and left to stand, aged for 8 hours, washed with water under reduced pressure and filtered for 3 times to obtain a filter cake. The filter cake is blast-dried at 60°C for 6 hours and crushed into fine particles, then placed in a muffle furnace for sintering for 8 hours at a sintering temperature of 145°C, dried at 80°C and the...
Embodiment 3
[0017] Dissolve 10g of commercially available commercially pure ruthenium trichloride in 150ml of deionized water, add 5ml of anhydrous low-molecular alcohol (isopropanol) and fuming hydrochloric acid during the dissolution process, stir vigorously for 30 minutes, and continue stirring after completely dissolving In the case of DI water was added continuously until the pH of the solution reached 6.7. Add ammonium bicarbonate with a concentration of 0.5M to the reaction system by spraying, and add 4ml of hydrogen peroxide to the system by spraying while continuing to stir the reaction liquid, keep stirring the reaction liquid for 30 minutes, let it stand, and age for 10 hours Then wash and filter under reduced pressure for 3 times to obtain a filter cake. The filter cake is blast-dried at 60°C for 6 hours and crushed into fine particles, then placed in a muffle furnace for sintering for 8 hours at a sintering temperature of 160°C, dried at 80°C and then ball-milled to finally o...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More