CN1594498A - Yttrium gallate based trichromatic fluorescent material and method for making same - Google Patents

Yttrium gallate based trichromatic fluorescent material and method for making same Download PDF

Info

Publication number
CN1594498A
CN1594498A CN 200410025792 CN200410025792A CN1594498A CN 1594498 A CN1594498 A CN 1594498A CN 200410025792 CN200410025792 CN 200410025792 CN 200410025792 A CN200410025792 A CN 200410025792A CN 1594498 A CN1594498 A CN 1594498A
Authority
CN
China
Prior art keywords
gallic acid
acid yttrium
fluorescent material
yttrium base
fluorescence
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.)
Granted
Application number
CN 200410025792
Other languages
Chinese (zh)
Other versions
CN100336885C (en
Inventor
李永祥
徐志华
王东
刘志甫
葛万银
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.)
Shanghai Institute of Ceramics of CAS
Original Assignee
Shanghai Institute of Ceramics of CAS
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 Shanghai Institute of Ceramics of CAS filed Critical Shanghai Institute of Ceramics of CAS
Priority to CNB2004100257924A priority Critical patent/CN100336885C/en
Publication of CN1594498A publication Critical patent/CN1594498A/en
Application granted granted Critical
Publication of CN100336885C publication Critical patent/CN100336885C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Images

Landscapes

  • Luminescent Compositions (AREA)

Abstract

The invention discloses an yttrium gallate based trichromatic fluorescent material and method for making same by using yttrium oxide (Y2O3), gallium oxide (Ga2O3), europium oxide (Eu2O3), terbium oxide (Tb4O7), and bismuth oxide (Bi2O3) as raw material through solid-phase sintering method, the synthesized material has the chemical formula of Y#-[3(1-x)]M#-[3x]Ga#-[5]O#-[12], wherein M is Eu or Tb or Bi (x=0.001-0.20).

Description

A kind of gallic acid yttrium base three fluorescence material and preparation method thereof
Technical field
The present invention relates to a kind of gallic acid yttrium base three fluorescence material and preparation method thereof, belong to the fluorescent material field.
Background technology
Fluorescent material is mainly used in technical fields such as illumination and display device, and wherein sulfide and oxide compound (comprising oxysalt) are the two big class materials that are most widely used.In the last few years in field of display, various flat pannel display (Flat Panel Display, FPD) technology obtains flourish, but sulfide luminescent material in the technique of display of electroluminescent demonstration (ELD), Field Emission Display (FED) and vacuum fluorescence demonstration active illuminating types such as (VFD), such as ZnS:Cu, Al, ZnS:Ag, Cl, GdOS:Tb, SrGa 2S 4: Eu etc. are also using at present widely, but sulfide material poor chemical stability, to decompose the infringement cause components and parts be to need a problem solving for a long time to sulfide under electron-bombardment, and it has water vapor sensitive, behind the life-time service under the luminous efficiency degradation shortcoming not only the manufacturing process of device is had higher requirement, and influence the permanent stability of device.These shortcomings are that sulfide intrinsic chemical property causes, and are difficult to improve by research.Chemical stability is good, material category is many and the metal oxide luminescent material has, and obtains advantages such as three primary colours easily, becomes the splendid candidate who replaces sulfide material, is one of research focus in this field in the world in recent years.At lighting field, with the metal oxide fluorescent RE powder of matrix owing to have under narrowband emission, short ultraviolet (185nm) radiation that advantages such as luminous intensity is stable have obtained good application under good stability, the high temperature in many novel florescent lamps, as three-color fluorescent lamp, compact fluorescent lamp, high color rendering index (CRI) lamp and some high-quality special lamps of using.Therefore development research is that the phosphor material powder of matrix can play very big promoter action for the development of flat pannel display and lighting engineering with the novel metal oxide.
The a collection of in the last few years novel metal oxide fluorescent material that has very much application prospect obtains research and development in succession, as ZnGa 2O 4, ZnGa 2O 4: Mn, SrTiO 3: Pr etc., but these materials are compared gap in addition with the sulfide material that tradition is used aspect luminescent properties, still can not perfect marketizations, and further explore the novel metal oxide luminescent material and seem and be necessary very much.Gallic acid yttrium (Y 3Ga 5O 12) have an A 3B 5O 12The garnet structure of type has chemical stability with Heat stability is good, compare characteristics such as synthesis temperature is lower with other metal oxide fluorescent materials, up to the present also is not the research report of matrix fluorescent material with the gallic acid yttrium.
Summary of the invention
The objective of the invention is synthetic a kind of be the metal oxide fluorescent material of matrix with the gallic acid yttrium, for the set lights under the different application environment and display device provide a class new fluorescent material.
The prescription of gallic acid yttrium base fluorescent material is as follows: with Y 2O 3(analytical pure), Ga 2O 3(analytical pure) is main component, respectively with Eu 2O 3(analytical pure) or Tb 4O 7(analytical pure) or Bi 2O 3(analytical pure) is doping agent: according to chemical formula Y 3 (1-x)M 3xGa 5O 12Mix, M is Eu or Tb or Bi, and the variation range of x can from 0.001 to 0.2.
The preparation method is as follows: raw material, was calcined 2-4 hour down at 1000-1200 ℃, again through cooling off, grind, sieve the gallic acid yttrium base fluorescent material that can obtain different glow colors after 1-5 hour with the planetary ball mill batch mixing.
The chemical formula of the gallic acid yttrium base fluorescent material of preparation gained is Y 3 (1-x)M 3xGa 5O 12, M is Eu or Tb or Bi, the variation range of x can from 0.001 to 0.2.
The gallic acid yttrium series luminescent material synthesis temperature of the present invention's preparation is low, do not need fusing assistant, technology is simple, a calcination forms, can on same matrix, realize the red, green, blue three-color light-emitting, therefore luminous intensity has a good application prospect with the main aluminate serial fluorescent material of using is suitable at present.
This class material has advantages such as luminous intensity height, stable chemical performance, synthesis temperature be low, can be used as set lights and display device fluorescent material.
Description of drawings
Fig. 1 is gallic acid yttrium rouge and powder material Y 2.85Eu 0.15Ga 5O 12Emmission spectrum under the 254nm ultraviolet excitation.
Fig. 2 is the green powder material Y of gallic acid yttrium 2.85Tb 0.15Ga 5O 12Emmission spectrum under the 254nm ultraviolet excitation.
Fig. 3 is gallic acid yttrium blue powder material Y 2.85Bi 0.15Ga 5O 12Emmission spectrum under the 254nm ultraviolet excitation.
Embodiment
Embodiment 1.
Gallic acid yttrium rouge and powder material: press chemical formula Y 2.85Eu 0.15Ga 5O 12Prepare burden, take by weighing Y 2O 3(analytical pure) 6.44 grams; Ga 2O 3(analytical pure) 9.37 grams; Eu 2O 3(analytical pure) 0.53 gram.Their with planetary ball mill batch mixing after 3 hours, 1100 ℃ of following sintering 4 hours, again by cooling off, grind, sieving, just can be obtained gallic acid yttrium base red fluorescent powder, and under the 254nm ultraviolet excitation, the main glow peak of this fluorescent material is at 593nm and 612nm.
Embodiment 2.
The green powder material of gallic acid yttrium: press chemical formula Y 2.85Tb 0.15Ga 5O 12Prepare burden, take by weighing Y 2O 3(analytical pure) 6.44 grams; Ga 2O 3(analytical pure) 9.37 grams; Tb 4O 7(analytical pure) 0.67 gram.Their with planetary ball mill batch mixing after 3 hours, 1100 ℃ of following sintering 4 hours, again through cooling off, grind, sieving, just can be obtained gallic acid yttrium base green emitting phosphor, and under the 254nm ultraviolet excitation, the main glow peak of this fluorescent material is at 543nm.
Embodiment 3.
Gallic acid yttrium blue powder material: press chemical formula Y 2.85Bi 0.15Ga 5O 12Prepare burden, take by weighing Y 2O 3(analytical pure) 6.44 grams; Ga 2O 3(analytical pure) 9.37 grams; Bi 2O 3(analytical pure) 0.70 gram.Their with planetary ball mill batch mixing after 3 hours, 1100 ℃ of following sintering 4 hours, again through cooling off, grind, sieving, just can be obtained gallic acid yttrium base blue colour fluorescent powder, and under the 254nm ultraviolet excitation, the main glow peak of this fluorescent material is at 454nm.

Claims (6)

1, a kind of gallic acid yttrium base three fluorescence material, the chemical formula that it is characterized in that this material is Y 3 (1-x)M 3xGa 5O 12, M is Eu or Tb or Bi, the variation range of x can from 0.001 to 0.2.
2, by the described a kind of gallic acid yttrium base three fluorescence preparation methods of claim 1, comprise the steps:
(1) with Y 2O 3, Ga 2O 3Be main component, respectively with Eu 2O 3Or Tb 4O 7Or Bi 2O 3Be doping agent, according to chemical formula Y 3 (1-x)M 3xGa 5O 12Prepare burden, M is Eu or Tb or Bi, the variation range of x from 0.001 to 0.2;
(2) batching after raw material through batch mixing, calcining, cooling, grinding, sieving to obtain gallic acid yttrium base fluorescent material.
3, by the described a kind of gallic acid yttrium base three fluorescence preparation methods of claim 1, it is characterized in that mixing time is 1-5 hour.
4,, it is characterized in that calcination condition is 1000-1200 ℃ and calcined 2-4 hour down by the described a kind of gallic acid yttrium base three fluorescence preparation methods of claim 1.
5, by claim 2 or 3 or 4 described a kind of gallic acid yttrium base three fluorescence preparation methods, it is characterized in that used raw material is more than the analytical pure level.
6, be used as set lights and display device fluorescent material by the described a kind of gallic acid yttrium base three fluorescence material of claim 1.
CNB2004100257924A 2004-07-06 2004-07-06 Yttrium gallate based trichromatic fluorescent material and method for making same Expired - Fee Related CN100336885C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2004100257924A CN100336885C (en) 2004-07-06 2004-07-06 Yttrium gallate based trichromatic fluorescent material and method for making same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2004100257924A CN100336885C (en) 2004-07-06 2004-07-06 Yttrium gallate based trichromatic fluorescent material and method for making same

Publications (2)

Publication Number Publication Date
CN1594498A true CN1594498A (en) 2005-03-16
CN100336885C CN100336885C (en) 2007-09-12

Family

ID=34663855

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2004100257924A Expired - Fee Related CN100336885C (en) 2004-07-06 2004-07-06 Yttrium gallate based trichromatic fluorescent material and method for making same

Country Status (1)

Country Link
CN (1) CN100336885C (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100519694C (en) * 2005-06-29 2009-07-29 北京大学 Y3(Al, ga)5O12rare earth fluorescent powder
CN109868507A (en) * 2017-12-05 2019-06-11 长春理工大学 A kind of New Type Magneto crystal Tb2YGa5O12(TYGG) preparation method
CN113755172A (en) * 2021-10-26 2021-12-07 长江大学 Fluorescent powder and preparation method thereof

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08170077A (en) * 1994-12-19 1996-07-02 Hitachi Ltd Fluorescent substance, its production, luminescent screen and cathode ray tube using the fluophor
JP3879298B2 (en) * 1999-01-22 2007-02-07 双葉電子工業株式会社 Field emission display

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100519694C (en) * 2005-06-29 2009-07-29 北京大学 Y3(Al, ga)5O12rare earth fluorescent powder
CN109868507A (en) * 2017-12-05 2019-06-11 长春理工大学 A kind of New Type Magneto crystal Tb2YGa5O12(TYGG) preparation method
CN113755172A (en) * 2021-10-26 2021-12-07 长江大学 Fluorescent powder and preparation method thereof
CN113755172B (en) * 2021-10-26 2023-11-14 长江大学 Fluorescent powder and preparation method thereof

Also Published As

Publication number Publication date
CN100336885C (en) 2007-09-12

Similar Documents

Publication Publication Date Title
CN101445729B (en) Preparation method of phosphor powder for white LED
CN101402857A (en) Red luminous material for LED and producing process thereof
CN110028964B (en) Dysprosium-silicon synergistic apatite structure blue-light fluorescent powder for white light LED and preparation method thereof
CN102352244B (en) LED red fluorescent material and its preparation method
CN1948426A (en) Preparation method of nanometer silicate long afterglow luminous material
CN109988575A (en) A kind of Eu3+Ion-activated vanadium phosphorus niobates red fluorescence powder, preparation method and applications
CN109181697A (en) A kind of niobates fluorescent powder of strong red emission and preparation method thereof
CN110484251B (en) Phosphor-aluminum acid strontium lithium sodium phosphor and preparation method thereof
CN112625683A (en) Germanate type red fluorescent powder and preparation method thereof
CN1952039A (en) Sialon fluorescent powder for white light LED and electric light sources manufactured therefrom
CN101760191B (en) High-brightness barium-silicate-based blue-green fluorescent powder for LED and high-temperature reducing preparation method thereof
CN100336885C (en) Yttrium gallate based trichromatic fluorescent material and method for making same
CN101463254B (en) Blue light excited orange fluorescent powder for white light LED and preparation thereof
CN110003901A (en) A kind of Eu3+And Ti4+Ion co-doped niobium tantalates red fluorescence powder, preparation method and applications
CN102320833B (en) Preparation method of Eu3+ doped yttrium lanthanum oxide transparent ceramic
CN102690659B (en) Orange red fluorescent powder for LED (Light Emitting Diode) and preparation method thereof
CN106833643B (en) A kind of green emitting phosphor and preparation method thereof of ultraviolet/near ultraviolet excitation
CN102071021A (en) Orange red fluorescent powder for LED and preparation method thereof
CN108070374A (en) A kind of white light emitting diode rubescent light luminescence rare earth material and preparation method thereof
CN111635756B (en) Non-rare earth fluorescent material with high quantum yield and synthetic method thereof
CN107541211A (en) Blue luminescent phosphor suitable near ultraviolet excitation and its preparation method and application
CN114479860A (en) Narrow-band green light fluorescent powder, preparation method thereof and white light LED light-emitting device
CN112480918A (en) Manganese-doped deep red light fluorescent powder material and preparation method thereof
CN103694998B (en) A kind of oxysulfide red long afterglow luminous material and preparation method thereof
CN101372617A (en) Blue fluorescent powder for field emission and vacuum fluorescence display and preparation thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20070912

Termination date: 20110706