Method for preparing hierarchical porous oxygen-rich carbon nanocones from organic metal complexes
A carbon nanocone and hierarchical porous technology, which is applied in the manufacture of hybrid/electric double layer capacitors, hybrid capacitor electrodes, electrochemical generators, etc., to achieve simple equipment and production processes, easy large-scale application, excellent cycle performance and rate performance Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0029] 0.811gFeCl 3 Dissolve in 50mL water, combine magnetic stirring and ultrasonic vibration to make FeCl 3 Fully dissolve. Dissolve 4.803g of o-hydroxybenzoic acid in 50mL of water, combine magnetic stirring and ultrasonic vibration to make FeCl 3 Fully dissolve. Then a homogeneous aqueous solution of o-hydroxybenzoic acid was slowly added to the FeCl 3 In the aqueous solution, stir at room temperature for 2h, once drop into the aqueous solution of o-hydroxybenzoic acid, FeCl 3 The aqueous solution changed from red to deep purple, and the solution began to become cloudy, indicating that the complexation reaction had occurred. After continuous magnetic stirring for 2 h, the obtained precipitate was centrifuged, dried, and then heat-treated in a tube furnace at 600° C. for 2 h under the protection of nitrogen, and finally hierarchical porous heteroatom-rich carbon nanocones were obtained. The prepared hierarchical porous heteroatom-rich carbon nanocone has a length of 2-...
Embodiment 2
[0031] 0.811gFeCl 3 Dissolve in 50mL water, combine magnetic stirring and ultrasonic vibration to make FeCl 3 Fully dissolve. Dissolve 4.803g of o-hydroxybenzoic acid in 50mL of water, combine magnetic stirring and ultrasonic vibration to make FeCl 3 Fully dissolve. Then the homogeneous o-hydroxybenzoic acid aqueous solution was slowly added dropwise to the FeCl 3 In the aqueous solution, stir at room temperature for 2h, once drop into the aqueous solution of o-hydroxybenzoic acid, FeCl 3 The aqueous solution changed from red to deep purple, and the solution began to become cloudy, indicating that the complexation reaction had occurred. After continuous magnetic stirring for 2 h, the obtained precipitate was centrifuged, dried, and then heat-treated in a tube furnace at 700° C. for 2 h under the protection of nitrogen, and finally hierarchical porous heteroatom-rich carbon nanocones were obtained. When used as a negative electrode material for lithium-ion batteries, at 50...
Embodiment 3
[0033] 2.02Fe(NO 3 ) 3 Dissolve in 50mL water, combine magnetic stirring and ultrasonic vibration to make Fe(NO 3 ) 3 Fully dissolve. Dissolve 4.803g of o-hydroxybenzoic acid in 50mL of water, combine magnetic stirring and ultrasonic vibration to make Fe(NO 3 ) 3 Fully dissolve. Then the homogeneous o-hydroxybenzoic acid aqueous solution was slowly added dropwise to the FeCl 3 In the aqueous solution, stir at room temperature for 2 hours, once the aqueous solution of o-hydroxybenzoic acid is dropped, Fe(NO 3 ) 3 The aqueous solution changed from red to deep purple, and the solution began to become cloudy, indicating that the complexation reaction had occurred. After continuous magnetic stirring for 2 h, the obtained precipitate was centrifuged, dried, and then heat-treated in a tube furnace at 600° C. for 2 h under the protection of nitrogen, and finally hierarchical porous heteroatom-rich carbon nanocones were obtained. The material has multifunctional energy storage...
PUM
Property | Measurement | Unit |
---|---|---|
length | aaaaa | aaaaa |
diameter | 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