Oxygen-vacancy-rich cobalt oxide nanocomposites doped with high-valence metal ions and its preparation and application
A nanocomposite material and metal ion technology, which is applied in the field of high-valence metal ion doped cobalt oxide nanocomposite rich in oxygen vacancies and its preparation, and achieves the effects of improving oxygen evolution performance, low overpotential and good reproducibility
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0042] Example 1: CoO x Preparation and Oxygen Evolution Performance (Undoped High-valence Metal Ions)
[0043] Get cobalt nitrate (0.582g, 2mmol) and dissolve in 20mL DI, get urea (0.6g, 10mmol) and dissolve in 20mL DI, after the two are mixed evenly, the solution is transferred to 50mL hydrothermal kettle; add pretreated 4 × 1cm The foamed nickel substrate was reacted at 120°C for 6 hours. After the reaction is completed, it is naturally cooled to room temperature, the foamed nickel substrate is taken out, washed several times with deionized water and absolute ethanol, and dried in vacuum at 60° C. for 12 hours to obtain the precursor material.
[0044] The prepared nickel foam (loaded with 0.01 g of precursor material) was placed in a porcelain boat, and 1.0 g of NaBH was weighed. 4 placed in another porcelain boat. loaded with NaBH 4 The porcelain boat is placed upstream, and the porcelain boat with nickel foam is placed in the middle section of the tube furnace. Unde...
Embodiment 2
[0047] Example 2: W / CoO x Preparation of -1 and its oxygen evolution properties
[0048] Take cobalt chloride (0.582g, 2.45mmol) and sodium tungstate (0.04g, 0.12mmol) and dissolve them in 20mL DI, take urea (0.6g, 10mmol) and dissolve them in 20mL DI, mix them well and transfer the solution to 50mL hydrothermal kettle; add the pretreated 4 × 1 cm nickel foam matrix, and react at 120 °C for 6 hours. After the reaction is completed, it is naturally cooled to room temperature, the foamed nickel substrate is taken out, washed several times with deionized water and absolute ethanol, and dried in vacuum at 60° C. for 12 hours to obtain the precursor material.
[0049] The prepared nickel foam (loaded with 0.007g of precursor material) was placed in the porcelain boat, and 1.0g of NaBH was weighed. 4 placed in another porcelain boat. loaded with NaBH 4 The porcelain boat is placed upstream, and the porcelain boat with nickel foam is placed in the middle section of the tube furna...
Embodiment 3
[0051] Example 3: Mo / CoO x Preparation of -2 and Its Oxygen Evolution Properties
[0052] Take cobalt acetate (0.582g, 2.3mmol), sodium molybdate (0.12g, 0.5mmol) and dissolve in 20mL DI, take urea (0.6g, 10mmol) and dissolve it in 20mL DI, mix the two and transfer the solution to 50mL In a hydrothermal kettle; add the pretreated 4×1cm nickel foam matrix, and react at 120°C for 6 hours. After the reaction is completed, it is naturally cooled to room temperature, the foamed nickel substrate is taken out, washed several times with deionized water and absolute ethanol, and dried in vacuum at 60° C. for 12 hours to obtain the precursor material.
[0053] The prepared nickel foam (loaded with 0.008g of precursor material) was placed in a porcelain boat, and 1.0g of NaBH was weighed. 4 placed in another porcelain boat. loaded with NaBH 4 The porcelain boat is placed upstream, and the porcelain boat with nickel foam is placed in the middle section of the tube furnace. In a nitro...
PUM
Property | Measurement | Unit |
---|---|---|
thickness | 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