Nitride red light conversion master batch and preparation method thereof
A light-converting masterbatch and nitride technology, which is applied in the direction of chemical instruments and methods, luminescent materials, etc., can solve the problems of short fluorescence life, poor matching, high preparation cost, etc., and achieve high luminous efficiency, small doping ratio, and terminal cost low effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0053] (1) Synthesis of nitride red light conversion agent: weigh Ca respectively according to stoichiometric ratio 3 N 2 ,Sr 3 N 2 ,ZnO,AlN,Si 3 N 4 , Eu 2 o 3 After fully mixing, transfer it to a boron nitride crucible for heating, then transfer it to a graphite furnace, and react at 1700°C for 4 hours under a high-purity nitrogen environment. After cooling, perform powder selection, crushing, and sieving to obtain sample A1. A1 is red.
[0054] The composition formula of sample A1 is: (Ca 0.950 Sr 0.04 Zn 0.010 ) 0.988 AlSiN 3 :Eu 0.012
[0055] For absorption and excitation spectra see figure 1 . figure 1 It shows that the red light conversion agent (A1) can effectively absorb ultraviolet light and yellow-green light that are not absorbed or are weakly absorbed by plant photosynthesis, and emit red light with a wavelength of 600nm-780nm required by plant photosynthesis. The action spectra are in good agreement.
[0056] (2) Preparation of nitride light con...
Embodiment 2
[0061] (1) Synthesis of nitride red light conversion agent: weigh Ca respectively according to stoichiometric ratio 3 N 2 ,Sr 3 N 2 , BaCO 3 ,MgO,AlN,Si 3 N 4 , Eu 2 o 3 ,NH 4 After Cl is fully mixed, heat it in a molybdenum nitride crucible, then transfer it to a graphite furnace, and react at 1850°C for 4 hours in a high-purity nitrogen environment. After cooling, perform powder selection, crushing, and sieving to obtain samples. It is orange-red, and the general formula of the sample composition is: (Ca 0.800 Sr 0.050 Ba 0.100 Mg 0.050 ) 0.980 AlSiN 3 :Eu 0.018 , Cl - 0.002
[0062] Experiments have proved that the excitation spectrum of the sample is the same as that of A1, which can effectively absorb ultraviolet light and yellow-green light that are not absorbed or are weakly absorbed by plant photosynthesis, and emit red light with a wavelength of 600nm-780nm required by plant photosynthesis. It is in good agreement with the photosynthesis spectrum.
...
Embodiment 3
[0068] (1) Synthesis of nitride red light conversion agent: weigh Ca respectively according to stoichiometric ratio 3 N 2 ,ZnO,AlN,Si 3 N 4 , Eu 2 o 3 , After KCl is fully mixed, it is transferred to a molybdenum nitride crucible for heating, then transferred to a graphite furnace, and reacted at 1800°C for 6 hours under a high-purity nitrogen environment. The sample is orange-red, and the general formula of the sample composition is: (Ca 0.990 Zn 0.010 ) 0.985 AlSiN 3 :Eu 0.012 , K + 0.003
[0069] Experiments have proved that the excitation spectrum of the sample is the same as that of A1, which can effectively absorb ultraviolet light and yellow-green light that are not absorbed or are weakly absorbed by plant photosynthesis, and emit red light with a wavelength of 600nm-780nm required by plant photosynthesis. It is in good agreement with the photosynthesis spectrum.
[0070] (2) Preparation of nitride light converting agent masterbatch
[0071]Get the sample ...
PUM
Property | Measurement | Unit |
---|---|---|
wavelength | aaaaa | aaaaa |
wavelength | aaaaa | aaaaa |
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