Preparation method of supercapacitor electrode material nickel and cobalt composite nanometer oxide
A technology of supercapacitors and nano-oxides, which is applied in the manufacture of hybrid capacitor electrodes and hybrid/electric double-layer capacitors, etc., to achieve the effects of easy-to-obtain raw materials, simple preparation methods, and low prices
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0026] (1) Weigh nickel acetate tetrahydrate (C 4 h 6 NiO 4 4H 2 O), cobalt acetate tetrahydrate (C 4 h 6 CoO 4 4H 2 (2) and urea, the corresponding quality is respectively 0.474g, 0.948g and 1.08g, is dissolved in 30mL deionized water, stirs 20 minutes, three are dissolved completely, then adds 0.5mL ethanolamine, continues to stir again 10 minutes to obtain mixed solution ;
[0027] (2) Pour the obtained mixed solution into a polytetrafluoroethylene hydrothermal reaction kettle to maintain a filling degree of 61%, then place the hydrothermal reaction kettle in a blast drying oven at 120°C for hydrothermal reaction for 24 hours, and then Cool the reactor to room temperature to obtain the reaction product;
[0028] (3) The obtained reaction product was centrifuged, washed with deionized water and ethanol respectively, and dried, and the dried sample was placed in a muffle furnace and calcined at 300°C (the heating rate was 5°C / min) for 3 hours to obtain The final prod...
Embodiment 2
[0034] (1) Weigh nickel acetate tetrahydrate (C 4 h 6 NiO 4 4H 2 O), cobalt acetate tetrahydrate (C 4 h 6 CoO 4 4H 2 (2) and urea, the corresponding quality is respectively 0.474g, 0.948g and 1.08g, is dissolved in 30mL deionized water, stirs 20 minutes, makes the three dissolve completely, then adds 1.0mL ethanolamine, continues to stir again 10 minutes to obtain mixed solution ;
[0035] (2) Pour the resulting mixed solution into a polytetrafluoroethylene hydrothermal reaction kettle to maintain a filling degree of 62%, then place the hydrothermal reaction kettle in a blast drying oven at 110°C for hydrothermal reaction for 48 hours, and then Cool the reactor to room temperature to obtain the reaction product;
[0036] (3) The obtained reaction product was centrifuged, washed with deionized water and ethanol respectively, and dried, and the dried sample was calcined in a muffle furnace at 350°C (heating rate: 5°C / min) for 3 hours to obtain The final product is super...
Embodiment 3
[0038] (1) Weigh nickel acetate tetrahydrate (C 4 h6 NiO 4 4H 2 O), cobalt acetate tetrahydrate (C 4 h 6 CoO 4 4H 2 (2) and urea, the corresponding quality is respectively 0.474g, 0.948g and 1.08g, is dissolved in 30mL deionized water, stirs 20 minutes, three are dissolved completely, then adds 0.5mL ethanolamine, continues to stir again 10 minutes to obtain mixed solution ;
[0039] (2) Pour the obtained mixed solution into a polytetrafluoroethylene hydrothermal reaction kettle to maintain a filling degree of 61%, then place the hydrothermal reaction kettle in a blast drying oven at 120°C for hydrothermal reaction for 24 hours, and then Cool the reactor to room temperature to obtain the reaction product;
[0040] (3) The obtained reaction product was centrifuged, washed with deionized water and ethanol respectively, and dried, and the dried sample was calcined in a muffle furnace at 400°C (the heating rate was 5°C / min) for 3 hours to obtain The final product is superc...
PUM
Property | Measurement | Unit |
---|---|---|
Diameter | aaaaa | aaaaa |
Specific capacitance | aaaaa | aaaaa |
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