Carbon nitride/titanium dioxide nanosheet array heterojunction photocatalyst and preparation method
A nanosheet array and titanium dioxide technology, applied in the direction of catalyst activation/preparation, physical/chemical process catalysts, chemical instruments and methods, etc., can solve the problem of easy recombination of photogenerated electrons/holes, uneven recombination of composite materials, and solar energy utilization. Low-level problems, to achieve the effect of improving photocatalytic hydrogen production activity, good commercial application prospects, and improving photocatalytic activity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0025] (1) g-C 3 N 4 preparation of
[0026] Accurately weigh 10g of urea and transfer it into an alumina crucible, put the crucible into a muffle furnace, raise the temperature to 550°C at a rate of 10°C / min, and keep it for 3h to obtain a light yellow powder g-C 3 N 4 The crude product was ground, washed successively with deionized water, 0.4% HCl solution, 1% NaOH solution, and finally washed with deionized water until neutral, and dried at 60°C for 12 hours to obtain pure yellow powder g-C 3 N 4 . Then, accurately measure 50mL of isopropanol and transfer it into a beaker, add 150mg of the obtained pure g-C 3 N 4 , ultrasonic dispersion for 30min to obtain pure g-C 3 N 4 exfoliation dispersion. (2)g-C 3 N 4 / TiO 2 Precursor preparation
[0027] Replace the above g-C 3 N 4 Transfer the exfoliation dispersion liquid into a hydrothermal kettle, add 21mL isopropanol, then add 0.09mL diethylenetriamine and 4.5mL isopropyl titanate in sequence, mix the solution ev...
Embodiment 2
[0033] (1) g-C 3 N 4 preparation of
[0034] Accurately weigh 10g of urea and transfer it into an alumina crucible, put the crucible into a muffle furnace, raise the temperature to 550°C at a rate of 10°C / min, and keep it for 3h to obtain a light yellow powder g-C 3 N 4 The crude product was ground, washed successively with deionized water, 0.4% HCl solution, 1% NaOH solution, and finally washed with deionized water until neutral, and dried at 60°C for 12 hours to obtain pure yellow powder g-C 3 N 4 . Then, accurately measure 50mL of isopropanol and transfer it into a beaker, add 50mg of the obtained pure g-C 3 N 4 , ultrasonic dispersion for 30min to obtain pure g-C 3 N 4 exfoliation dispersion. (3) g-C 3 N 4 / TiO 2 Precursor preparation
[0035] Replace the above g-C 3 N 4 Transfer the exfoliation dispersion liquid into a hydrothermal kettle, add 21mL isopropanol, then add 0.09mL diethylenetriamine and 4.5mL isopropyl titanate in sequence, mix the solution ev...
Embodiment 3
[0039] (1) g-C 3 N 4 preparation of
[0040] Accurately weigh 10g of urea and transfer it into an alumina crucible, put the crucible into a muffle furnace, raise the temperature to 550°C at a rate of 10°C / min, and keep it for 3h to obtain a light yellow powder g-C 3 N 4 The crude product was ground, washed successively with deionized water, 0.4% HCl solution, 1% NaOH solution, and finally washed with deionized water until neutral, and dried at 60°C for 12 hours to obtain pure yellow powder g-C 3 N 4 . Then, accurately measure 50mL of isopropanol into a beaker, add 100mg of the obtained pure g-C 3 N 4 , ultrasonic dispersion for 30min to obtain pure g-C 3 N 4 exfoliation dispersion. (2)g-C 3 N 4 / TiO 2 Precursor preparation
[0041]Replace the above g-C 3 N 4 Transfer the exfoliation dispersion liquid into a hydrothermal kettle, add 21mL isopropanol, then add 0.09mL diethylenetriamine and 4.5mL isopropyl titanate in sequence, mix the solution evenly, react at 20...
PUM
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