JPH0665571A - Blue emitting phosphor - Google Patents

Blue emitting phosphor

Info

Publication number
JPH0665571A
JPH0665571A JP6374692A JP6374692A JPH0665571A JP H0665571 A JPH0665571 A JP H0665571A JP 6374692 A JP6374692 A JP 6374692A JP 6374692 A JP6374692 A JP 6374692A JP H0665571 A JPH0665571 A JP H0665571A
Authority
JP
Japan
Prior art keywords
phosphor
thulium
compd
baking
yttrium
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
JP6374692A
Other languages
Japanese (ja)
Inventor
Shunichi Kubota
俊一 窪田
Hirotane Takizawa
博胤 滝沢
Tadashi Endo
忠 遠藤
Masahiko Shimada
昌彦 島田
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.)
Mitsubishi Kasei Corp
Original Assignee
Mitsubishi Kasei Corp
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 Mitsubishi Kasei Corp filed Critical Mitsubishi Kasei Corp
Priority to JP6374692A priority Critical patent/JPH0665571A/en
Publication of JPH0665571A publication Critical patent/JPH0665571A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a thulium-activated yttrium tantalate phosphor which exhibits a blue emission with a high color purity when excited by a electron beams, ultraviolet rays, or X-rays by increasing the amt. of activation by thuli um. CONSTITUTION:This phosphor represented by the general formula: (Y1-xTmx)Ta7 O19 (wherein (x) is 1X10<-2> or higher, pref. 2X10<-2=x<=1.2X10<-1>) is produced by thoroughly mixing specified amts. of a yttrium compd., a thulium compd., and a tantalum compd. with a flux such as ammonium chloride or fluoride by the or dry method, baking the mixture at least once at 800-1,600 deg.C in air or in an inert atmosphere for 1-12hr provided the last baking is carried out at 100 deg.C or above, and grinding, washing, drying, and sifting the baking product.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、電子線、紫外線及びX
線の励起によって青色発光を示すツリウム付活イットリ
ウムタンタル酸塩蛍光体に関する。
BACKGROUND OF THE INVENTION The present invention relates to electron beams, ultraviolet rays and X-rays.
The present invention relates to a thulium-activated yttrium tantalate phosphor that emits blue light when excited by a line.

【0002】[0002]

【従来の技術】ツリウム(Tm3+)やセリウム(C
3+)を付活剤とする蛍光体は、一般に色純度の良い青
色発光を示すため、種々の研究がなされている。特にT
m付活の蛍光体として実用化が検討されている蛍光体と
しては、例えばツリウム付活イットリウムアルミン酸塩
蛍光体(YAlO3 :Tm)等が知られている。しかし
ながらYAlO3 :Tm蛍光体は良好な色純度を示すも
のの、輝度の点で不十分であるため、より高輝度の蛍光
体が求められていた。
2. Description of the Related Art Thulium (Tm 3+ ) and cerium (C
Since phosphors using e 3+ ) as an activator generally emit blue light with good color purity, various studies have been conducted. Especially T
As a phosphor that is being put into practical use as an m-activated phosphor, for example, a thulium-activated yttrium aluminate phosphor (YAlO 3 : Tm) is known. However, although the YAlO 3 : Tm phosphor exhibits good color purity, it is insufficient in terms of brightness, and therefore a phosphor with higher brightness has been demanded.

【0003】[0003]

【発明が解決しようとする課題】そこで、本発明者等は
Tmを付活剤とする色純度の良い青色発光蛍光体であっ
て高輝の蛍光体を得るべく研究を重ねた結果、Tmの付
活量を増加させると、本来発光強度は増大すべきものが
蛍光体母体の構造により濃度消光現象が生じ、発光強度
が大きくならない事を見出した。
Therefore, the inventors of the present invention have conducted research to obtain a high-luminance phosphor that is a blue light-emitting phosphor that has Tm as an activator and has good color purity. It has been found that when the activity is increased, the emission intensity should originally be increased, but the concentration quenching phenomenon occurs due to the structure of the phosphor matrix, and the emission intensity is not increased.

【0004】即ち、Tm付活蛍光体の発光強度を向上さ
せるためには、母体中に多くのTmを発光中心として取
り込ませてもいかに濃度消光が始まらないようにするか
が重要な着眼点である。このため濃度消光の原因である 1.共鳴伝達による交差緩和 2.共鳴伝達による非発光中心へのエネルギー回遊 等を考慮する必要がある。共鳴伝達がTmイオン間距離
RのR-nに比例することから、共鳴伝達を抑えるため
に、Tmイオンの置換されるサイト間距離が長いことが
母体には求められる。しかし、Tmイオン間での共鳴伝
達が起こらないようなサイト間距離を母体自身に求める
ことや、Tmイオンをそのような距離で等間隔で置換す
ることは困難であると考えられる。そこで次に、共鳴伝
達による非発光中心へのエネルギー回遊をいかに抑える
かが問題となる。エネルギー回遊によって「ある一定時
間内に励起エネルギーが移動できる結晶内の空間の体
積」が大きい程、欠陥などの非発光中心に会う機会が多
くなる。このとき、発光中心となるTmイオンが結晶中
において、より低次元(1,2次元)に配置されていれ
ば、励起エネルギーが同じ格子点を訪れる確率が大きく
なるため「移動できる体積」は小さくなり、非発光中心
への励起エネルギーの回遊は抑えられる。
That is, in order to improve the emission intensity of the Tm-activated phosphor, it is important to consider how the concentration quenching does not start even if a large amount of Tm is incorporated into the matrix as an emission center. is there. This is the cause of concentration quenching. Cross relaxation by resonance transfer 2. It is necessary to consider energy migration to non-radiative centers due to resonance transfer. Since the resonance transfer is proportional to R −n of the distance R between Tm ions, the distance between sites where Tm ions are replaced is required to be long in the mother body in order to suppress the resonance transfer. However, it is considered difficult to determine the distance between sites in the matrix itself such that resonance transfer between Tm ions does not occur, or to replace Tm ions with such a distance at equal intervals. Then, the next issue is how to suppress the energy migration to the non-radiative center due to resonance transmission. The larger the “volume of the space in the crystal in which the excitation energy can be transferred within a certain period of time” due to energy migration, the greater the chance of meeting non-radiative centers such as defects. At this time, if the Tm ions, which are the luminescence centers, are arranged in a lower dimension (one-dimensional or two-dimensional) in the crystal, the probability that the excitation energy visits the same lattice point increases, so that the “movable volume” is small. Therefore, the migration of the excitation energy to the non-radiative centers is suppressed.

【0005】以上のような点から、Tmを付活剤とする
蛍光体の母体として適していると考えられるものは、酸
化物の場合、発光中心となるTmイオンの置換されるサ
イト同士が、他のカチオンと酸素イオンが形成するクラ
スターによって離され、しかも低次元に配置されたよう
な結晶構造をもつ化合物である。このような化合物とし
ては、ホウ酸塩、リン酸塩などが一般に考えられるが、
本発明者等は高温安定性、化学的安定性等により優れて
いると考えられる、特定のタンタル酸塩が母体として最
適であると判断し、発光強度と色純度の良好なTmを付
活剤とするタンタル酸塩青色蛍光体を提供しようとする
ものである。
From the above points, in the case of an oxide, what is considered to be suitable as a matrix of a phosphor having Tm as an activator is that the sites where the Tm ions, which are the emission centers, are substituted. It is a compound having a crystal structure such that it is separated by a cluster formed by other cations and oxygen ions, and is arranged in a low dimension. As such a compound, borate, phosphate, etc. are generally considered,
The inventors of the present invention have determined that a specific tantalate salt, which is considered to be excellent in high-temperature stability, chemical stability, etc., is the most suitable as a base material, and has Tm with good emission intensity and color purity as an activator. The present invention is intended to provide a tantalate blue phosphor.

【0006】[0006]

【課題を解決するための手段】本発明は一般式(Y1-X
Tmx )Ta7 19で表され、式中のxは1×10-2
上であることを特徴とする青色発光蛍光体である。本発
明の新規な蛍光体は、電子線、紫外線及びX線の励起に
より青色発光を示す。本発明の蛍光体は次のようにして
合成することができる。
The present invention has the general formula (Y 1 -X
The blue-emitting phosphor is represented by Tm x ) Ta 7 O 19 and x in the formula is 1 × 10 −2 or more. The novel phosphor of the present invention emits blue light when excited by electron beams, ultraviolet rays and X-rays. The phosphor of the present invention can be synthesized as follows.

【0007】蛍光体原料として、 1)酸化イットリウム、しゅう酸イットリウム、炭酸イ
ットリウム等のイットリウム化合物。 2)酸化ツリウム、しゅう酸ツリウム、炭酸ツリウム等
のツリウム化合物 3)五酸化タンタル、塩化タンタル等のタンタル化合物
を所定量秤量し、塩化アンモニウム、弗化アンモニウム
等のフラックスを配合し、原料混合物を充分に湿式又は
乾式混合する。尚、イットリウムとツリウム希土類同志
は共沈にて混合してもよい。
As the phosphor raw material, 1) yttrium compounds such as yttrium oxide, yttrium oxalate, and yttrium carbonate. 2) Thulium compounds such as thulium oxide, thulium oxalate, and thulium carbonate 3) Weigh a predetermined amount of tantalum compounds such as tantalum pentoxide and tantalum chloride, add a flux of ammonium chloride, ammonium fluoride, etc., and mix the raw material mixture sufficiently. Wet or dry mix. The yttrium and the thulium rare earth elements may be mixed by coprecipitation.

【0008】この混合物をルツボ等の耐熱容器に充填
し、空気中もしくは中性雰囲気中800〜1600℃で
1〜12時間1回以上焼成する。尚、最終焼成は必ず1
100℃以上とする。この焼成物を粉砕、水洗、乾燥、
篩を行い、本発明の青色発光のタンタル酸塩蛍光体を得
ることができる。
This mixture is filled in a heat-resistant container such as a crucible and fired once or more at 800 to 1600 ° C. in air or a neutral atmosphere for 1 to 12 hours. The final firing is always 1
The temperature is 100 ° C or higher. This fired product is crushed, washed with water, dried,
By performing sieving, the blue light emitting tantalate phosphor of the present invention can be obtained.

【0009】[0009]

【作用】図1は、本発明の(Y1-x Tmx )Ta7 19
蛍光体(○印)と周知の(Y1- x Tmx )AlO3 蛍光
体(△印)を紫外線(365nm)で励起した場合の発
光強度とTm濃度(x)との関係を示す図である。図1
で明らかな如く、本発明の蛍光体はxが1×10-2以上
で有意な発光強度を示し、又、xが2×10-2以上にお
いて周知の(Y1-x Tmx )AlO3 蛍光体に比べ発光
強度が高い。特にxの上限値は1.4×10-1、より好
ましくは1.2×10-1である。
FIG. 1 shows (Y 1-x Tm x ) Ta 7 O 19 of the present invention.
FIG. 3 is a diagram showing the relationship between the emission intensity and the Tm concentration (x) when the phosphor (◯ mark) and the well-known (Y 1- x Tm x ) AlO 3 phosphor (Δ mark) are excited by ultraviolet rays (365 nm). is there. Figure 1
As is clear from the above, the phosphor of the present invention shows a significant emission intensity when x is 1 × 10 -2 or more, and the known (Y 1-x Tm x ) AlO 3 when x is 2 × 10 -2 or more. The emission intensity is higher than that of a phosphor. In particular, the upper limit value of x is 1.4 × 10 -1 , and more preferably 1.2 × 10 -1 .

【0010】図2は、紫外線365nm励起下での本発
明の(Y0.93Tm0.007 )Ta7 19蛍光体の発光スペ
クトルを示す。発光は456nmにピークを持つTmイ
オン特有の色純度の良好な青色発光スペクトルを示し
た。
FIG. 2 shows the actual emission under excitation of ultraviolet rays of 365 nm.
Ming (Y0.93Tm0.007) Ta7O 19Luminescent emission of phosphor
Show Koutor. The emission is Tm with a peak at 456 nm.
Shows a good blue emission spectrum with a unique color purity of ON
It was

【0011】[0011]

【実施例】 (実施例)[Example] (Example)

【0012】[0012]

【表1】 表 1 Y2 3 2.1g (0.93モル) Tm2 3 0.3g (0.07モル) Ta2 5 30.9g (7.0モル) NH4 Cl 0.3g (0.6モル)Table 1 Table 1 Y 2 O 3 2.1 g (0.93 mol) Tm 2 O 3 0.3 g (0.07 mol) Ta 2 O 5 30.9 g (7.0 mol) NH 4 Cl 0. 3 g (0.6 mol)

【0013】上記各原料を充分硝酸溶液中で混合し、蒸
発乾固後、空気中に於て800℃で3時間焼成した。得
られた焼成物を粉砕後1200℃で更に4時間焼成し、
粉砕、水洗、乾燥、篩を行い蛍光体を得た。この蛍光体
の組成は(Y0.93Tm0.07)Ta7 19であり、紫外線
365nm励起下で図1に示す発光スペクトルを示し
た。
The above raw materials were sufficiently mixed in a nitric acid solution, evaporated to dryness, and then calcined in air at 800 ° C. for 3 hours. After pulverizing the obtained fired product, it is further fired at 1200 ° C. for 4 hours,
The phosphor was obtained by crushing, washing with water, drying and sieving. The composition of this phosphor was (Y 0.93 Tm 0.07 ) Ta 7 O 19 and the emission spectrum shown in FIG.

【0014】[0014]

【発明の効果】本発明は、上記母体組成を採用すること
により、Tm濃度が高濃度付活の明るい青色蛍光体が可
能になり、電子管用、ランプ用及び増感紙用に好適な蛍
光体が得られた。
EFFECTS OF THE INVENTION The present invention makes it possible to provide a bright blue phosphor having a high Tm concentration by adopting the above-mentioned base composition, which is suitable for electron tubes, lamps and intensifying screens. was gotten.

【図面の簡単な説明】[Brief description of drawings]

【図1】Tm濃度(x)と発光強度の関係を示したグラ
フである。
FIG. 1 is a graph showing the relationship between Tm concentration (x) and emission intensity.

【図2】(Y0.93Tm0.07)Ta7 19蛍光体の発光ス
ペクトルを示したグラフである。
FIG. 2 is a graph showing an emission spectrum of a (Y 0.93 Tm 0.07 ) Ta 7 O 19 phosphor.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 島田 昌彦 宮城県仙台市青葉区荒巻字青葉(番地な し) 東北大学工学部内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Masahiko Shimada Aoba, Aoba-ku, Sendai-shi, Miyagi Aoba (No house number), Faculty of Engineering, Tohoku University

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 一般式(Y1-X Tmx )Ta7 19で表
され、式中のxは1×10-2以上であることを特徴とす
る青色発光蛍光体。
1. A represented by the general formula (Y 1-X Tm x) Ta 7 O 19, a blue-emitting phosphor, wherein the x in the formula is 1 × 10 -2 or more.
【請求項2】 請求項1記載の青色発光蛍光体におい
て、xが2×10-2≦x≦1.2×10-1の範囲にある
ことを特徴とする青色発光蛍光体。
2. The blue light-emitting phosphor according to claim 1, wherein x is in the range of 2 × 10 −2 ≦ x ≦ 1.2 × 10 −1 .
JP6374692A 1992-03-19 1992-03-19 Blue emitting phosphor Pending JPH0665571A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6374692A JPH0665571A (en) 1992-03-19 1992-03-19 Blue emitting phosphor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6374692A JPH0665571A (en) 1992-03-19 1992-03-19 Blue emitting phosphor

Publications (1)

Publication Number Publication Date
JPH0665571A true JPH0665571A (en) 1994-03-08

Family

ID=13238278

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6374692A Pending JPH0665571A (en) 1992-03-19 1992-03-19 Blue emitting phosphor

Country Status (1)

Country Link
JP (1) JPH0665571A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0820773A (en) * 1994-07-01 1996-01-23 Rhone Poulenc Chim Use of tantalate doped with yttrium, lutetium or gadolinium in low-voltage luminescence
JP2015040226A (en) * 2013-08-20 2015-03-02 学校法人東海大学 Upconversion type phosphor and method of manufacturing the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0820773A (en) * 1994-07-01 1996-01-23 Rhone Poulenc Chim Use of tantalate doped with yttrium, lutetium or gadolinium in low-voltage luminescence
JP2015040226A (en) * 2013-08-20 2015-03-02 学校法人東海大学 Upconversion type phosphor and method of manufacturing the same

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