CN109929553B - Borophosphate orange-red fluorescent powder and preparation method and application thereof - Google Patents
Borophosphate orange-red fluorescent powder and preparation method and application thereof Download PDFInfo
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- CN109929553B CN109929553B CN201811594355.2A CN201811594355A CN109929553B CN 109929553 B CN109929553 B CN 109929553B CN 201811594355 A CN201811594355 A CN 201811594355A CN 109929553 B CN109929553 B CN 109929553B
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- 239000000843 powder Substances 0.000 title claims abstract description 68
- 238000002360 preparation method Methods 0.000 title abstract description 15
- 239000000126 substance Substances 0.000 claims abstract description 7
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 25
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 14
- 238000000227 grinding Methods 0.000 claims description 13
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 12
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 12
- 229910052808 lithium carbonate Inorganic materials 0.000 claims description 11
- 238000005245 sintering Methods 0.000 claims description 10
- 229910017677 NH4H2 Inorganic materials 0.000 claims description 9
- 238000004321 preservation Methods 0.000 claims description 9
- FKTOIHSPIPYAPE-UHFFFAOYSA-N samarium(III) oxide Inorganic materials [O-2].[O-2].[O-2].[Sm+3].[Sm+3] FKTOIHSPIPYAPE-UHFFFAOYSA-N 0.000 claims description 9
- 230000005284 excitation Effects 0.000 claims description 8
- 230000008569 process Effects 0.000 claims description 8
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 108010043121 Green Fluorescent Proteins Proteins 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 4
- 239000012535 impurity Substances 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 239000002245 particle Substances 0.000 claims description 4
- 238000005303 weighing Methods 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims 1
- 238000004020 luminiscence type Methods 0.000 abstract description 2
- YZYDPPZYDIRSJT-UHFFFAOYSA-K boron phosphate Chemical compound [B+3].[O-]P([O-])([O-])=O YZYDPPZYDIRSJT-UHFFFAOYSA-K 0.000 abstract 1
- 229910000149 boron phosphate Inorganic materials 0.000 abstract 1
- 239000002994 raw material Substances 0.000 description 9
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 4
- 230000002596 correlated effect Effects 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 238000005286 illumination Methods 0.000 description 4
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 3
- 229910052593 corundum Inorganic materials 0.000 description 2
- 239000010431 corundum Substances 0.000 description 2
- 238000004134 energy conservation Methods 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000000695 excitation spectrum Methods 0.000 description 2
- 238000012544 monitoring process Methods 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 230000001133 acceleration Effects 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 238000009529 body temperature measurement Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229940097139 perfect choice Drugs 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02B—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO BUILDINGS, e.g. HOUSING, HOUSE APPLIANCES OR RELATED END-USER APPLICATIONS
- Y02B20/00—Energy efficient lighting technologies, e.g. halogen lamps or gas discharge lamps
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- Luminescent Compositions (AREA)
Abstract
The invention discloses borophosphate orange red fluorescent powder and a preparation method and application thereof, wherein the chemical formula of the fluorescent powder isX is more than or equal to 0.01 and less than or equal to 0.04. The borophosphate orange-red fluorescent powder disclosed by the invention is boron phosphate orange-red fluorescent powder which can be excited by near ultraviolet light, can be excited by a near ultraviolet light LED chip to realize orange-red luminescence, and is used as a component of tricolor fluorescent powder for outputting white light.
Description
Technical Field
The invention relates to fluorescent powder, in particular to borophosphate orange-red fluorescent powder and a preparation method and application thereof.
Background
In recent years, with the acceleration of urbanization and the application of new-generation information technologies such as the internet, urban lighting has made higher demands on artificial lighting technologies, and intelligent lighting, healthy lighting, and green lighting have become hot directions for people to study.
Due to the excellent light, color and electricity controllability of the LED, the LED becomes a perfect choice for a green illumination light source. As a novel all-solid-state lighting source, the white light LED has the advantages of energy conservation, environmental protection, high luminous efficiency, high stability, low voltage, extremely high response speed, small volume, long service life, strong designability and the like, has replaced incandescent lamps, fluorescent lamps and high-pressure mercury lamps to become a fourth generation lighting source, and is regarded as one of the most important green lighting sources in the new century because of wide application prospect and market.
At present, the LED illumination market at home and abroad is briskly developed, the policy of continuously banning the selling of incandescent lamps in all countries in the world is popularized, the global LED industry is advanced in the mature period, and the application technologies of white light LEDs, ultraviolet LEDs, vehicle LEDs, intelligent illumination, plant illumination and the like are continuously developed.
In LED lighting, the development of white LED technology has become one of the hot research spots in the optical field. At present, one of the technical ways to realize white light of an LED is to add three primary colors fluorescent powder to obtain white light with high luminous efficiency. However, red phosphors capable of being excited by ultraviolet light are still lacking in the market.
Most of red fluorescent powder with higher conversion efficiency is a sulfide system, but the sulfide has poor luminous stability and chemical stability, so that the performance attenuation is serious in the working process, and the large-scale application of the red fluorescent powder is limited. Therefore, there is a need to develop a novel red phosphor with high luminous efficiency, good stability and excellent performance.
Disclosure of Invention
The invention aims to provide borophosphate orange-red fluorescent powder, a preparation method and application thereof, the fluorescent powder solves the problem of low luminous efficiency of the existing sulfide system, and has the advantages of high color purity, low correlated color temperature, low raw material price and the like.
In order to achieve the purpose, the invention provides a borophosphate orange-red fluorescent powder, and the chemical formula of the fluorescent powder is0.01≤x≤0.04。
Preferably, the fluorescent powder is effectively excited by near ultraviolet light with the wavelength of 350-400 nm.
Preferably, the emission centers of the fluorescent powder are positioned at 561nm, 597nm, 643nm and 699nm under the excitation wavelength of 400 nm.
The invention also provides a preparation method of the borophosphate orange-red fluorescent powder, which comprises the following steps:
(1) mixing Li2CO3Anhydrous Na2CO3、H3BO3、NH4H2PO4And Sm2O3Sintering the powder at 300-450 ℃, and keeping the temperature to remove gas and impurities generated in the reaction process;
(2) after the heat preservation is finished, sintering at 550-650 ℃, preserving heat, and repeating the process of taking out the powder, grinding and preserving heat for a plurality of times in the heat preservation process;
(3) and after the heat preservation is finished, cooling and grinding to obtain the borophosphate orange-red fluorescent powder.
Preferably, the method further comprises: weighing Li2CO3Anhydrous Na2CO3、H3BO3、NH4H2PO4And Sm2O3And grinding to obtain powder with uniform particles.
Preferably, in step (1), the Li2CO3Anhydrous Na2CO3、H3BO3、NH4H2PO4And Sm2O3The weight ratio of (A) to (B) is 0.369: 0.260: 0.309: 1.150: 0.017.
preferably, in the step (1), the powder is sintered and insulated for 5 hours at 400 ℃ in a resistance furnace.
Preferably, in the step (2), the powder is sintered and insulated for 24 hours in a resistance furnace at 600 ℃.
The present invention also provides a white light LED, comprising: the LED fluorescent lamp comprises red fluorescent powder, green fluorescent powder, blue fluorescent powder and an LED chip for exciting the fluorescent powder; wherein the red phosphor comprises: the borophosphate is orange-red fluorescent powder.
The borophosphate orange-red fluorescent powder, the preparation method and the application thereof solve the problem of low luminous efficiency of the existing sulfide system, and have the following advantages:
(1) the borophosphate orange-red fluorescent powder can be excited by near ultraviolet light, can be excited by a near ultraviolet light LED chip to realize orange-red luminescence, and is used as a component of tricolor fluorescent powder for outputting white light;
(2) the borophosphate orange-red fluorescent powder disclosed by the invention is high in color purity and low in correlated color temperature, the color purity is over 85%, and the correlated color temperature is 2104-2483K;
(3) the invention takes the borophosphate as a matrix material, and has the advantages of low price of raw materials, low sintering temperature, mild reaction condition, energy conservation, environmental protection, good thermal stability and the like;
(4) the preparation method provided by the invention is simple and efficient, the adopted raw materials are easy to obtain, the cost is low, the popularization is easy, and the preparation method is suitable for large-scale industrial production;
(5) sm is selected and used in the invention3+Sm ion as activator in orange red fluorescent powder3+Ions can be effectively excited under ultraviolet light, and orange red light with main peaks at 561, 597, 643 and 699nm wavelengths is emitted;
(6) the green fluorescent powder has stronger luminous performance under the excitation of ultraviolet light with the wavelength of 400nm, can be well matched with a near ultraviolet LED chip (350-400nm), and can be used as fluorescent powder for a white light LED based on the ultraviolet LED chip.
Drawings
Fig. 1 is an XRD diffraction pattern of the borophosphate orange-red phosphor of example 1 of the present invention.
Fig. 2 is an excitation spectrum obtained by the borophosphate orange-red phosphor of embodiment 1 of the present invention at a monitoring wavelength of 597 nm.
FIG. 3 is a spectrum of light emitted from borophosphate orange-red phosphor of examples 1-4 of the present invention at an excitation wavelength of 400 nm.
FIG. 4 is a graph showing the relationship between the luminous intensity and the value of x of the borophosphate orange-red phosphor.
FIG. 5 is a CIE chromaticity coordinate diagram of the borophosphate orange-red phosphor of the present invention taken at a wavelength of 400 nm.
Detailed Description
The technical solutions in the embodiments of the present invention will be clearly and completely described below, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
Further, the fluorescent powder is effectively excited by near ultraviolet light with the wavelength of 350-400 nm.
Further, the emission centers of the phosphors at an excitation wavelength of 400nm are located at 561nm, 597nm, 643nm, and 699 nm.
The invention also provides a preparation method of the borophosphate orange-red fluorescent powder, which comprises the following steps:
(1) mixing Li2CO3Anhydrous Na2CO3、H3BO3、NH4H2PO4And Sm2O3Sintering the powder at 300-450 ℃, and keeping the temperature to remove gas and impurities generated in the reaction process;
(2) after the heat preservation is finished, sintering at 550-650 ℃, preserving heat, and repeating the process of taking out the powder, grinding and preserving heat for a plurality of times in the heat preservation process;
(3) and after the heat preservation is finished, cooling and grinding to obtain the borophosphate orange-red fluorescent powder.
Further, the method further comprises: weighing Li2CO3Anhydrous Na2CO3、H3BO3、NH4H2PO4And Sm2O3And grinding to obtain powder with uniform particles.
Further, in the step (1), Li2CO3Anhydrous Na2CO3、H3BO3、NH4H2PO4And Sm2O3The weight ratio of (A) to (B) is 0.369: 0.260: 0.309: 1.150: 0.017.
further, in the step (1), the powder is sintered and insulated for 5 hours at 400 ℃ in a resistance furnace.
Further, in the step (2), the powder is sintered and insulated for 24 hours in a resistance furnace at 600 ℃.
The present invention also provides a white light LED, comprising: the LED fluorescent lamp comprises red fluorescent powder, green fluorescent powder, blue fluorescent powder and an LED chip for exciting the fluorescent powder; wherein, the red phosphor comprises: borophosphate orange-red phosphor.
More specifically, the borophosphate green phosphor and the preparation method thereof provided by the present invention are described in detail below with reference to examples 1 to 4.
(1) weighing 0.369g Li according to stoichiometric ratio2CO30.260g of anhydrous Na2CO3、0.309g H3BO3、1.150gNH4H2PO4And 0.017g Tb4O7Fully grinding the weighed reactant in a mortar until powder with uniform particles is obtained;
(2) after uniform mixing, transferring the mixture into a corundum crucible, placing the corundum crucible into a box-type resistance furnace, pre-sintering at 400 ℃, and keeping the temperature for 5 hours so as to remove gas and other impurities generated in the reaction process;
(3) taking out and grinding, sintering at 600 ℃, preserving heat for 1 day at 600 ℃, taking out and grinding for many times in the process of preserving heat, ensuring that reactants are in full contact, reducing agglomeration of powder and ensuring that experiments are carried out completely and fully;
(4) cooling to room temperature, taking out the sample, and grinding to obtainThe green phosphor, as shown in FIG. 1, is an XRD diffraction pattern obtained by sintering at 600 ℃ in example 1 of the present invention.
As shown in FIG. 2, which is an excitation spectrum obtained by the borophosphate orange-red phosphor of embodiment 1 of the present invention at a monitoring wavelength of 597nm, it can be seen from the graph that the positions of the excitation peaks are respectively located at 343, 361, 374, 400, 415-420, and 438nm, which respectively correspond to Sm3+Ion(s)6H5/2→4D9/2,6H5/2→4D3/2,6H5/2→4D1/2,6H5/2→(4F7/2+6P3/2),6H5/2→(6P5/2+4P5/2),6H5/2→4G9/2Is detected. Of these, the strongest excitation peak is located at 400 nm.
The preparation method is basically the same as that of the example 1, except that the dosage of each raw material is different, and the specific dosage of the raw material is Li2CO3:0.369g,Na2CO3:0.262g,H3BO3:0.309g,NH4H2PO4:1.150g,Tb4O7:0.009g。
The preparation method is basically the same as that of the example 1, except that the dosage of each raw material is different, and the specific dosage of the raw material is Li2CO3:0.369g,Na2CO3:0.257g,H3BO3:0.309g,NH4H2PO4:1.150g,Tb4O7:0.026g。
The preparation method is basically the same as that of the example 1, except that the dosage of each raw material is different, and the specific dosage of the raw material is Li2CO3:0.369g,Na2CO3:0.254g,H3BO3:0.309g,NH4H2PO4:1.150g,Tb4O7:0.035g。
The experimental results are as follows:
as shown in FIG. 3, which is a spectrum of the emission light of the borophosphate orange-red phosphor of examples 1-4 of the present invention at an excitation wavelength of 400nm, it can be seen that the emission centers are located at 561, 597, 643 and 699nm, respectively, wherein the maximum emission light is obtained at 597 nm.
As shown in FIG. 4, it is a graph of the relationship between the luminous intensity of borophosphate orange red fluorescent powder and the value of x, and Sm is shown in the graph3+The optimum doping amount of (3) is 0.02 mol.
As shown in fig. 5, which is a CIE chromaticity diagram of the borophosphate orange-red phosphor of the present invention obtained at a wavelength of 400nm, it can be seen that the color coordinates of the sample are located in the orange-red region on the CIE chromaticity diagram.
Color purity and color temperature measurements of examples 1-5, example 1Color purity of (2) was 85%, of example 2Color purity of (2) 85%, example 3Color purity of 86%, example 4The color purity of (2) was 96%. Examples 1 to 4The correlated color temperature of (2) is 2104-2483K.
While the present invention has been described in detail with reference to the preferred embodiments, it should be understood that the above description should not be taken as limiting the invention. Various modifications and alterations to this invention will become apparent to those skilled in the art upon reading the foregoing description. Accordingly, the scope of the invention should be determined from the following claims.
Claims (10)
2. The borophosphate orange-red phosphor of claim 1, wherein the phosphor is effectively excited by near ultraviolet light having a wavelength of 350-400 nm.
3. The borophosphate orange-red phosphor of claim 2, wherein the phosphor has emission centers at 561nm, 597nm, 643nm, and 699nm at an excitation wavelength of 400 nm.
5. A method of making the borophosphate orange-red phosphor of any of claims 1-4, comprising:
(1) mixing Li2CO3Anhydrous Na2CO3、H3BO3、NH4H2PO4And Sm2O3Sintering the powder at 300-450 ℃, and keeping the temperature to remove gas and impurities generated in the reaction process;
(2) after the heat preservation is finished, sintering at 550-650 ℃, preserving heat, and repeating the process of taking out the powder, grinding and preserving heat for a plurality of times in the heat preservation process;
(3) and after the heat preservation is finished, cooling and grinding to obtain the borophosphate orange-red fluorescent powder.
6. The method of claim 5, further comprising: weighing Li2CO3Anhydrous Na2CO3、H3BO3、NH4H2PO4And Sm2O3And grinding to obtain powder with uniform particles.
7. The method of claim 5, wherein in step (1), the Li is added to the phosphor2CO3Anhydrous Na2CO3、H3BO3、NH4H2PO4And Sm2O3The weight ratio of (A) to (B) is 0.369: 0.260: 0.309: 1.150: 0.017.
8. the method for preparing borophosphate orange-red fluorescent powder according to claim 5, wherein in the step (1), the powder is sintered and insulated for 5 hours at 400 ℃ in a resistance furnace.
9. The method for preparing borophosphate orange-red fluorescent powder according to claim 5, wherein in the step (2), the powder is sintered and insulated in a resistance furnace at 600 ℃ for 24 hours.
10. A white LED, comprising: the LED fluorescent lamp comprises red fluorescent powder, green fluorescent powder, blue fluorescent powder and an LED chip for exciting the fluorescent powder; wherein the red phosphor comprises: the borophosphate orange-red phosphor of any one of claims 1-4.
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