Indium tin oxide compound and its preparation method and photocatalytic application
A technology of indium tin oxide and compounds, which is applied in the fields of indium tin oxide compounds and its preparation and photocatalysis application, and can solve the problems of pressing the door, harsh preparation and process conditions, etc.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0033] Example 1: 0.90SnO 2 :0.10In compound
[0034] Taking stannous chloride, indium chloride and potassium hydroxide as starting materials, weigh 4.50 mmol of stannous chloride and 0.5 mmol of indium chloride, dissolve them in 70 mL of deionized water, and stir for 10 minutes to make It mixes evenly; Add 10 mmol potassium hydroxide to the above-mentioned mixed solution, continue stirring for 30 minutes to obtain a clear solution; Put the clear solution into a hydrothermal reaction kettle for heat treatment, control the temperature at 160 o C, continuous reaction for 12 hours, and then the reacted solution was separated to obtain a precipitate; the obtained precipitate was washed 10 times with deionization, and dried at 60°C for 4 hours to obtain the final product.
[0035] The plasma emission spectrum of the synthesized product shows the actual composition and theoretical composition of indium tin oxide material 0.90SnO 2 :0.10In close. figure 1 The 0.90SnO prepared for ...
Embodiment 2
[0037] Example 2: 0.80SnO 2 :0.20In compound
[0038]Taking stannous chloride, indium chloride, and potassium hydroxide as starting materials, weigh 8 mmol of stannous chloride and 2 mmol of indium chloride, dissolve them in 70 mL of deionized water, and stir for 10 minutes to make It mixes evenly; Add 10mmol ammoniacal liquor to above-mentioned mixed solution, continue stirring for 30 minutes to obtain clear solution; Clear solution is put into hydrothermal reaction kettle and carry out heat treatment, control temperature 180 o C, continuous reaction for 24 hours, and then the reacted solution was separated to obtain a precipitate; the obtained precipitate was washed 10 times with deionization, and dried at 60°C for 4 hours to obtain the final product.
[0039] The plasma emission spectrum of the synthesized product shows the actual composition and theoretical composition of indium tin oxide material 0.80SnO 2 :0.20In close. Figure 5 0.80SnO prepared for this example 2 :...
Embodiment 3
[0041] Example 3: 0.70SnO 2 :0.30In compound
[0042] Using stannous nitrate, indium nitrate, and urea as starting materials, weigh 2.8 mmol of stannous nitrate and 1.2 mmol of indium nitrate, dissolve the two in 70 mL of deionized water, and stir for 10 minutes to mix them evenly; Add 15mmol urea to the mixed solution, and continue to stir for 30 minutes to obtain a clear solution; the clear solution is put into a hydrothermal reactor for heat treatment, and the temperature is controlled at 100 o C, continuous reaction for 48 hours, and then the reacted solution was separated to obtain a precipitate; the obtained precipitate was washed 10 times with deionization, and dried at 60°C for 4 hours to obtain the final product.
[0043] The plasma emission spectrum of the synthesized product shows the actual composition and theoretical composition of indium tin oxide material 0.70SnO 2 :0.30In close. Figure 9 0.70SnO prepared for this example 2 : The X-ray diffraction pattern o...
PUM
| Property | Measurement | Unit |
|---|---|---|
| particle diameter | aaaaa | aaaaa |
| diameter | aaaaa | aaaaa |
| diameter | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More - R&D
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com



