CN103849394A - Lanthanum gallate luminescent material and preparation method thereof - Google Patents

Lanthanum gallate luminescent material and preparation method thereof Download PDF

Info

Publication number
CN103849394A
CN103849394A CN201210499959.5A CN201210499959A CN103849394A CN 103849394 A CN103849394 A CN 103849394A CN 201210499959 A CN201210499959 A CN 201210499959A CN 103849394 A CN103849394 A CN 103849394A
Authority
CN
China
Prior art keywords
luminescent material
lanthanum gallate
span
preparation
cala
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201210499959.5A
Other languages
Chinese (zh)
Inventor
周明杰
王荣
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Oceans King Lighting Science and Technology Co Ltd
Shenzhen Oceans King Lighting Science and Technology Co Ltd
Shenzhen Oceans King Lighting Engineering Co Ltd
Original Assignee
Oceans King Lighting Science and Technology Co Ltd
Shenzhen Oceans King Lighting Engineering Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Oceans King Lighting Science and Technology Co Ltd, Shenzhen Oceans King Lighting Engineering Co Ltd filed Critical Oceans King Lighting Science and Technology Co Ltd
Priority to CN201210499959.5A priority Critical patent/CN103849394A/en
Publication of CN103849394A publication Critical patent/CN103849394A/en
Pending legal-status Critical Current

Links

Abstract

The invention belongs to the field of luminescent materials and discloses a lanthanum gallate luminescent material and a preparation method thereof. The lanthanum gallate luminescent material has a general molecular formula of CaLa1-xGa3-yO7: Dy<x><3+>, Sny; and in the general molecular formula, Sn is used as a doping element, x is >0 and <=0.2, and y is > 0 and <= 0.1. The lanthanum gallate luminescent material utilizes the Sn element and the Sn element can produce sensitization effects on rare earth ions in the lanthanum gallate luminescent material. Compared with a luminescent material without the Sn element, the lanthanum gallate luminescent material provided by the invention has greatly improved luminescence properties under the excitation condition of same emitted light wavelength. Therefore, the lanthanum gallate luminescent material has good luminescence properties.

Description

A kind of lanthanum gallate calcium luminescent material and preparation method thereof
Technical field
The present invention relates to field of light emitting materials, relate in particular to a kind of preparation method of lanthanum gallate calcium luminescent material.
Background technology
Field Emission Display (FED) is a kind of flat panel display that has very much development potentiality.The operating voltage of field emission display is lower than the operating voltage of cathode tube (CRT), be conventionally less than 5kV, and working current density is relatively large, generally at 10~100 μ Acm -2.Therefore, higher to the requirement of the luminescent powder for Field Emission Display, as to have better saturation, luminous efficiency under low voltage higher and under high current density without luminance saturation phenomenon etc.At present, the research of Field Emission Display luminescent powder is mainly concentrated on to two aspects: the one, utilize and improve existing cathode tube luminescent powder; The 2nd, find new luminescent material.Commercial cathodoluminescence powder, take sulfide as main, in the time being used for fabricating yard emission display screen, because sulphur wherein can react with Microamounts of Mo, silicon or germanium etc. in negative electrode, thereby having weakened its electron emission, and then has affected the performance of whole device.Exist potential using value in luminescent material Application Areas.
In the fluorescent material that feds adopts at present, there is a type oxide series fluorescence
Powder, gallate luminous material wherein, doping with rare-earth ions is luminous, has the advantages that stability is good, and still, the gallate luminous material luminous efficiency of preparing in prior art is not high, has limited its application in illumination and demonstration field.
Summary of the invention
The lanthanum gallate calcium luminescent material that provides a kind of luminous efficiency higher is provided problem to be solved by this invention.
Technical scheme of the present invention is as follows:
A kind of lanthanum gallate calcium luminescent material, its general molecular formula is: CaLa 1-xga 3-yo 7: Dy x 3+, Sn y; Wherein, Sn is doped element, and the span of x is 0 < x≤0.2, and the span of y is 0 < y≤0.1; Preferably, the span of x is 0.001≤x≤0.1, and the span of y is 0.005≤y≤0.05.
The present invention also provides the preparation method of above-mentioned lanthanum gallate calcium luminescent material, comprises the steps:
According to molecular formula CaLa 1-xga 3-yo 7: Dy x 3+, Sn yin the metering of each element chemistry ratio, respectively compound and the SnO to contain Ca, La, Ga and Dy 2for raw material, by even all raw material ground and mixed, process 1 ~ 8h at 900 ~ 1400 ℃ of temperature lower calcinations, be cooled to room temperature, the molecular formula that obtains Sn and be doped element is CaLa 1-xga 3-yo 7: Dy x 3+, Sn ylanthanum gallate calcium luminescent material;
Wherein, the span of x is 0 < x≤0.2, and the span of y is 0 < y≤0.1.
The preparation method of described lanthanum gallate calcium luminescent material, preferably, the compound of Ca, La, Ga, Dy is respectively the oxide compound, carbonate, oxalate, nitrate or the muriate that contain Ca, La, Ga, Dy.
The preparation method of described lanthanum gallate calcium luminescent material, preferably, the span of x is 0.001≤x≤0.1, the span of y is 0.005≤y≤0.05.
The preparation method of described lanthanum gallate calcium luminescent material, preferably, when described calcination processing, calcining temperature is 900 ~ 1200 ℃, calcination time is 2 ~ 6h.
Lanthanum gallate calcium luminescent material of the present invention, introduce Sn element, sensibilized by Sn element to luminescent material Rare Earth Ion, compared with not introducing the luminescent material of Sn element, the luminescent properties of this luminescent material under the shooting conditions of same transmit optical wavelength is greatly improved, and therefore luminescent properties is good.
Preparation method's processing step of the present invention is few, and technique is simple, with low cost, can be widely used in the manufacture of luminescent material, and the lanthanum gallate calcium luminescent material obtaining do not introduce other impurity, and quality is high.
Accompanying drawing explanation
Fig. 1 is that lanthanum gallate calcium luminescent material prepared by the embodiment of the present invention 4 is the luminescent spectrum comparison diagram under the cathode-ray exciting under 1.5KV with contrast luminescent material at acceleration voltage; Wherein, curve 1 is lanthanum gallate calcium luminescent material prepared by embodiment 4: the CaLa of doping Sn element 0.95ga 2.98o 7: Dy 0.05 3+, Sn 0.02the luminescent spectrum of luminescent material, curve 2 is contrast luminescent materials: the CaLa of the Sn element that do not adulterate 0.95ga 2.98o 7: Dy 0.05 3+the luminescent spectrum of luminescent material.
Embodiment
Below in conjunction with accompanying drawing, preferred embodiment of the present invention is described in further detail.
Embodiment 1:CaLa 0.9ga 2.95o 7: Dy 0.1 3+, Sn 0.05:
Preparation method: adopt CaCl 2, LaCl 3, GaCl 3, DyCl 3and SnO 2for main raw material, take CaCl 20.4439g, LaCl 30.8829g, GaCl 32.0777g, DyCl 30.1075g, SnO 20.0301g, mixes above-mentioned raw materials to be placed in High Temperature Furnaces Heating Apparatus, at 900 ℃, calcines 6h, and calcinate cools to room temperature with the furnace, and obtained product is ground to powder, and obtaining chemical formula is CaLa 0.9ga 2.95o 7: Dy 0.1 3+, Sn 0.05lanthanum gallate calcium luminescent material.
Embodiment 2:CaLa 0.999ga 2.9o 7: Dy 0.001 3+, Sn 0.1
Preparation method: adopt CaCO 3, La 2(CO 3) 3, Ga 2(CO 3) 3, Dy 2(CO 3) 3and SnO 2for main raw material, take CaCO 30.4004g, La 2(CO 3) 30.9147g, Ga 2(CO 3) 31.8529g, Dy 2(CO 3) 30.0010g, SnO 20.0602g, mixes above-mentioned raw materials to be placed in High Temperature Furnaces Heating Apparatus, at 1200 ℃, calcines 2h, and calcinate cools to room temperature with the furnace, and obtained product is ground to powder, and obtaining chemical formula is CaLa 0.999ga 2.9o 7: Dy 0.001 3+, Sn 0.1lanthanum gallate calcium luminescent material.
Embodiment 3:CaLa 0.8ga 2.999o 7: Dy 0.2 3+, Sn 0.001:
Preparation method: adopt Ca (NO 3) 2, La (NO 3) 3, Ga (NO 3) 3, Dy (NO 3) 3and SnO 2for main raw material, take Ca (NO 3) 20.6563g, La (NO 3) 31.0397g, Ga (NO 3) 33.0678g, Dy (NO 3) 30.2788g, SnO 20.0006g, mixes above-mentioned raw materials to be placed in High Temperature Furnaces Heating Apparatus, at 1400 ℃, calcines 1h, and calcinate cools to room temperature with the furnace, and obtained product is ground to powder, and obtaining chemical formula is CaLa 0.8ga 2.999o 7: Dy 0.2 3+, Sn 0.001lanthanum gallate calcium luminescent material.
Embodiment 4:CaLa 0.95ga 2.98o 7: Dy 0.05 3+, Sn 0.02:
Preparation method: adopt CaO, La 2o 3, Ga 2o 3, Dy 2o 3and SnO 2for main raw material, take CaO0.2243g, La 2o 30.6190g, Ga 2o 31.1171g, Dy 2o 30.0373g, SnO 20.0120g, mixes above-mentioned raw materials to be placed in High Temperature Furnaces Heating Apparatus, at 1100 ℃, calcines 5h, and calcinate cools to room temperature with the furnace, and obtained product is ground to powder, and obtaining chemical formula is CaLa 0.95ga 2.98o 7: Dy 0.05 3+, Sn 0.02lanthanum gallate calcium luminescent material.
Fig. 1 is that lanthanum gallate calcium luminescent material prepared by the embodiment of the present invention 4 is the luminescent spectrum comparison diagram under the cathode-ray exciting under 1.5KV with contrast luminescent material at acceleration voltage; Wherein, curve 1 is lanthanum gallate calcium luminescent material prepared by embodiment 4: the CaLa of doping Sn element 0.95ga 2.98o 7: Dy 0.05 3+, Sn 0.02the luminescent spectrum of luminescent material, curve 2 is contrast luminescent materials: the CaLa of the Sn element that do not adulterate 0.95ga 2.98o 7: Dy 0.05 3+the luminescent spectrum of luminescent material.
As can be seen from Figure 1,, at the emission peak at 575nm place, after doping Sn element, the luminous intensity of the luminous intensity of luminescent material before not adulterating strengthened 27%.
Embodiment 5:CaLa 0.85ga 2.995o 7: Dy 0.15 3+, Sn 0.005:
Preparation method: adopt CaC 2o 4, La2 (C2O4) 3, Ga 2o 3, and SnO 2for main raw material, take CaC 2o 40.5124g, La 2(C 2o 4) 30.8225g, Ga 2(C 2o 4) 32.1295g, Dy 2(C 2o 4) 30.1623g, SnO 20.0030g, mixes above-mentioned raw materials to be placed in High Temperature Furnaces Heating Apparatus, at 900 ℃, calcines 8h, and calcinate cools to room temperature with the furnace, and obtained product is ground to powder, and obtaining chemical formula is CaLa 0.85ga 2.995o 7: Dy 0.15 3+, Sn 0.005gallate luminous material.
Embodiment 6:CaLa 0.92ga 2.92o 7: Dy 0.08 3+, Sn 0.08:
Preparation method: adopt CaCO 3, La 2o 3, Ga 2o 3, Dy 2o 3and SnO 2for main raw material, take CaCO 30.4004g, La 2o 30.5995g, Ga 2o 31.0946g, Dy 2o 30.0597g, SnO 20.0482g, mixes above-mentioned raw materials to be placed in High Temperature Furnaces Heating Apparatus, at 1300 ℃, calcines 3h, and calcinate cools to room temperature with the furnace, and obtained product is ground to powder, and obtaining chemical formula is CaLa 0.92ga 2.92o 7: Dy 0.08 3+, Sn 0.08gallate luminous material.
Should be understood that, the above-mentioned statement for preferred embodiment of the present invention is comparatively detailed, can not therefore think the restriction to scope of patent protection of the present invention, and scope of patent protection of the present invention should be as the criterion with claims.

Claims (6)

1. a lanthanum gallate calcium luminescent material, is characterized in that, its general molecular formula is: CaLa 1-xga 3-yo 7: Dy x 3+, Sn y; Wherein, Sn is doped element, and the span of x is 0 < x≤0.2, and the span of y is 0 < y≤0.1.
2. lanthanum gallate calcium luminescent material according to claim 1, is characterized in that, the span of x is 0.001≤x≤0.1, and the span of y is 0.005≤y≤0.05.
3. a preparation method for lanthanum gallate calcium luminescent material, is characterized in that, comprises the steps:
According to molecular formula CaLa 1-xga 3-yo 7: Dy x 3+, Sn yin the metering of each element chemistry ratio, respectively compound and the SnO to contain Ca, La, Ga and Dy 2for raw material, by even all raw material ground and mixed, process 1 ~ 8h at 900 ~ 1400 ℃ of temperature lower calcinations, be cooled to room temperature, the molecular formula that obtains Sn and be doped element is CaLa 1-xga 3-yo 7: Dy x 3+, Sn ylanthanum gallate calcium luminescent material;
Wherein, the span of x is 0 < x≤0.2, and the span of y is 0 < y≤0.1.
4. the preparation method of lanthanum gallate calcium luminescent material according to claim 3, is characterized in that, the compound of Ca, La, Ga, Dy is respectively the oxide compound, carbonate, oxalate, nitrate or the muriate that contain Ca, La, Ga, Dy.
5. the preparation method of lanthanum gallate calcium luminescent material according to claim 3, is characterized in that, the span of x is 0.001≤x≤0.1, and the span of y is 0.005≤y≤0.05.
6. the preparation method of lanthanum gallate calcium luminescent material according to claim 3, is characterized in that, when described calcination processing, calcining temperature is 900 ~ 1200 ℃, and calcination time is 2 ~ 6h.
CN201210499959.5A 2012-11-29 2012-11-29 Lanthanum gallate luminescent material and preparation method thereof Pending CN103849394A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201210499959.5A CN103849394A (en) 2012-11-29 2012-11-29 Lanthanum gallate luminescent material and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201210499959.5A CN103849394A (en) 2012-11-29 2012-11-29 Lanthanum gallate luminescent material and preparation method thereof

Publications (1)

Publication Number Publication Date
CN103849394A true CN103849394A (en) 2014-06-11

Family

ID=50857525

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201210499959.5A Pending CN103849394A (en) 2012-11-29 2012-11-29 Lanthanum gallate luminescent material and preparation method thereof

Country Status (1)

Country Link
CN (1) CN103849394A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI717185B (en) * 2019-01-23 2021-01-21 億光電子工業股份有限公司 Near-infrared phosphor, optoelectronic device comprising the same, and method of preparing optoelectronic device
CN117363354A (en) * 2023-09-20 2024-01-09 枣庄学院 Tm3+ regulated dysprosium activated lanthanum calcium gallate white light fluorescent powder and preparation method and application thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000034479A (en) * 1998-07-17 2000-02-02 Kasei Optonix Co Ltd Rare earth composite oxide phosphor
CN1729268A (en) * 2002-12-20 2006-02-01 丰田合成株式会社 Luminescent body and optical device including the same

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000034479A (en) * 1998-07-17 2000-02-02 Kasei Optonix Co Ltd Rare earth composite oxide phosphor
CN1729268A (en) * 2002-12-20 2006-02-01 丰田合成株式会社 Luminescent body and optical device including the same

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
赵文玉等: "CaLaGa3O7:Dy3+荧光粉的光致和阴极射线发光性能", 《科学通报》 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI717185B (en) * 2019-01-23 2021-01-21 億光電子工業股份有限公司 Near-infrared phosphor, optoelectronic device comprising the same, and method of preparing optoelectronic device
CN117363354A (en) * 2023-09-20 2024-01-09 枣庄学院 Tm3+ regulated dysprosium activated lanthanum calcium gallate white light fluorescent powder and preparation method and application thereof

Similar Documents

Publication Publication Date Title
CN101760195B (en) Silicate blue luminescent material and preparation method thereof
CN102666783B (en) Borate luminous material and preparation method thereof
CN102618272A (en) Phosphate red luminescent material and preparation method thereof
CN103275713A (en) Rare earth molybdate red phosphor, and preparation method and application thereof
EP2597133B1 (en) Luminescent material of silicate and preparing method thereof
CN101812294A (en) White light emitting dysprosium-doped dodecacalcium heptaluminate fluorescent powder used for LED and preparation method thereof
CN102051170B (en) Calcium yttrium stannate light-emitting material doped with light-emitting ions and preparation method thereof
EP2915863B1 (en) Silicate luminescent material and preparation method therefor
CN103849394A (en) Lanthanum gallate luminescent material and preparation method thereof
CN104059658B (en) Gadolinium acid calcium luminescent material of doping In and/or Sn and preparation method thereof
CN102585818A (en) Rare earth niobium tantalate fluorescent powder with adjustable luminous chroma, preparation method and application thereof
CN102443394A (en) Vanadium phosphate phosphor and preparation method thereof
US8709284B2 (en) ZnO green luminescent material and its preparation
US20120068117A1 (en) Green luminescent materials and their preparing methods
CN103361053A (en) Silicate luminous material and preparation method thereof
CN102341478A (en) Oxide luminescent materials activated by trivalent thulium and their preparations
CN103849391B (en) Silicate luminescent material and preparation method thereof
CN104059666A (en) Sn-doped gallate red light luminescent material and preparation method thereof
CN101705091B (en) Yellow light-emitting rare earth luminescent material for field emission display and preparation method thereof
CN101717638A (en) Fluorescent powder for field emission and method for preparing same
CN102899042A (en) Pr, Eu/Tb co-doped tungstate/molybdate fluorescent powder and preparation method thereof
CN101962546B (en) Luminescent material and production method thereof
EP2505631B1 (en) Silicate luminescent material and its preparation method
CN102994083B (en) Tungstate based luminescent material as well as preparation method and application of tungstate based luminescent material
CN101864310A (en) Blue or green fluorescent material for field emission

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20140611