JPS59105234A - Cathode - Google Patents

Cathode

Info

Publication number
JPS59105234A
JPS59105234A JP57215751A JP21575182A JPS59105234A JP S59105234 A JPS59105234 A JP S59105234A JP 57215751 A JP57215751 A JP 57215751A JP 21575182 A JP21575182 A JP 21575182A JP S59105234 A JPS59105234 A JP S59105234A
Authority
JP
Japan
Prior art keywords
layer
emitting material
electron emitting
electron
base metal
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
JP57215751A
Other languages
Japanese (ja)
Inventor
Iwao Sato
佐藤 「巌」
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 Electric Corp
Original Assignee
Mitsubishi Electric 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 Electric Corp filed Critical Mitsubishi Electric Corp
Priority to JP57215751A priority Critical patent/JPS59105234A/en
Publication of JPS59105234A publication Critical patent/JPS59105234A/en
Pending legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J1/00Details of electrodes, of magnetic control means, of screens, or of the mounting or spacing thereof, common to two or more basic types of discharge tubes or lamps
    • H01J1/02Main electrodes
    • H01J1/13Solid thermionic cathodes
    • H01J1/14Solid thermionic cathodes characterised by the material

Abstract

PURPOSE:To improve an emission life by a simple means while enabling to perform stable electron emission for a long time by preparing a film-shaped barrier layer selected from high melting metals having transmission holes, between the first-and-second layers of an electron emission substance laid on the base metal. CONSTITUTION:A barrier layer 12 made of Ni is a film having one or plural transmission holes 13 while being prepared between the first layer 3 of an electron emission substance made of powder, wherein a ternary oxide of Ba, Sr and Ca is mixed with Zr, and the second layer 4 of the electron emission substance made of powder of the ternary oxide of Ba, Sr and Ca while both layers being prepared on the base metal 2 consisting of Mg acting as a reduction element and Ni containing silicon. Said barrier layer 12 can be obtained by means of vacuum evaporation of Ni on a mixture of the ternary carbonate of Ba, Sr and Ca, which are the starting substances of the ternary oxide laid on the base metal 2, and the hydrogenated zirconium by an ordinary spray method or the like.

Description

【発明の詳細な説明】 この発明は受像管などに用いられる陰極に関し、特に電
子放射層を改良した陰極に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a cathode used in a picture tube or the like, and particularly to a cathode with an improved electron emitting layer.

受像管の高性能化に伴って、高電流密度動作に長時間耐
えられる陰極の提奈が種々なされている。
As the performance of picture tubes has improved, various types of cathode tubes have been developed that can withstand high current density operation for long periods of time.

たとえば第1図に示すように、ニッケルを主成分とする
基体金属(2)上に電子放射物質第一層(3)、さらに
電子放射物質第一層(3)に積nして電子放射物質第二
層(4)を被着した溝成の陰極(1)がある。基体金属
(2)には不純物程度のシリコン、ジルコニウム、マグ
ネシウム、アルミニウムなどの還元性の強い元素が含ま
れている。電子放射物IR第二府(4)は複数種のアル
カリ土類金6の酸化物よシなり、通常アルカリ土類金属
群の中よシバリウム、ストロンチウム、カルシウムが選
ばれる。電子放射物質第一層(3)は電子放射物質第二
層(4)と同様にバリウム、ストロンチウム、カルシウ
ムよシなるアルカリ土類金属の酸化物を主成分とし、こ
れに0.011&−〜数−の還元性元素、たとえばジル
コニウム。
For example, as shown in Figure 1, the first layer of electron emitting material (3) is deposited on the base metal (2) mainly composed of nickel, and then the first layer of electron emitting material (3) is laminated with the electron emitting material. There is a grooved cathode (1) coated with a second layer (4). The base metal (2) contains highly reducing elements such as silicon, zirconium, magnesium, and aluminum, which are at the level of impurities. The electron emitter IR No. 2 (4) is composed of oxides of a plurality of alkaline earth metals, typically sybarium, strontium, and calcium from the alkaline earth metal group. The first layer of electron emitting material (3), like the second layer of electron emitting material (4), mainly contains oxides of alkaline earth metals such as barium, strontium, and calcium, and contains 0.011 - reducing elements such as zirconium.

ハフニウム、チタン等が含まれている。Contains hafnium, titanium, etc.

ところで、基体金属(2)、電子放射物質第一層(3)
、電子放射物質第二層(4)はヒータ(5)によって8
00℃程度に加熱される。したがって、基体金属(2)
中に含すれるシリコン、ジルコニウム、マグネシウム等
の元素と基体金属(2)に接する電子放射物質第一層(
3)のアルカリ土類金属酸化物との間で近元反応を生じ
、また電子放射物質第−j習(3)の中の前述シタジル
コニウム、ハフニウム等とアルカリ土類金属酸化物との
間で同様に還元反応が進み、遊たしたアルカリ土類金属
が生じる。遊だ(アルカリ土類金属は電子放射物質第一
層(3)および電子放射物質第二層(4)を拡散して電
子放射物質第二層(4)の表面に達し、ド九−レベルを
与えて熱電子放射を容易にする。前記還元反応の例を(
1) 、 (2)式に示す。
By the way, base metal (2), electron emitting material first layer (3)
, the second layer of electron emitting material (4) is heated to 8 by the heater (5).
It is heated to about 00°C. Therefore, base metal (2)
The first layer of electron-emitting material (
A near-element reaction occurs between the alkaline earth metal oxides in 3), and between the alkaline earth metal oxides and the aforementioned sitazirconium, hafnium, etc. Similarly, the reduction reaction proceeds and liberated alkaline earth metals are produced. (The alkaline earth metal diffuses through the first layer of electron-emitting material (3) and the second layer of electron-emitting material (4), reaches the surface of the second layer of electron-emitting material (4), and reaches the nine-level level. An example of the reduction reaction is (
1) and (2).

BaO+ Mg : Ba + MgO、、・・・・−
・・・(1)2EaO+Zr 4! 2Ba + Zr
O2−・−・・−・・・・(2)上記説明から理解でき
るように、電子放射物質第一層(3)は電子放射物質第
二層(4)に対してたとえば遊離バリウムの供給源とな
っている。
BaO+Mg: Ba+MgO,...-
...(1)2EaO+Zr 4! 2Ba + Zr
O2-・-・・・・・・・(2) As can be understood from the above explanation, the first layer of electron emitting material (3) is a source of free barium, for example, for the second layer of electron emitting material (4). It becomes.

しかしながら、以上の構成による従来の陰極(1)はエ
ミッション寿命特性の点で以下に述べる欠点があること
が判明した。すなわち、電子放射物質第一層(3)内で
生じた遊離バリウムは、電子放射物質第二層(4)の表
面に達したとき、その蒸気圧が高いために蒸発消耗が大
きくなる。(1)式を例にとると、(1)式の反応は平
衡反応であシ、バリウムの拡散、蒸発による消耗によシ
還元元素マグネシウムの消費を誘起する。したがって、
バリウムの消耗が早ければマグネシウムの消耗も早期に
きたし、エミッション員も早期に減少する。つまりエミ
ッション寿命特性は潤足すべきものが得られない。
However, it has been found that the conventional cathode (1) having the above configuration has the following drawbacks in terms of emission life characteristics. That is, when the free barium generated in the first layer of electron emitting material (3) reaches the surface of the second layer of electron emitting material (4), its vapor pressure is high, so that the free barium is consumed by evaporation to a large extent. Taking Equation (1) as an example, the reaction of Equation (1) is an equilibrium reaction, which induces consumption of the silica-reducing element magnesium through diffusion and evaporation of barium. therefore,
If barium is depleted quickly, magnesium is depleted quickly, and the number of emission members decreases quickly. In other words, the emission life characteristics cannot be satisfied.

さらに、バリウムの蒸発が多いことによってバリウムが
近接の電極構成部品へ付着し、電極同絶縁劣化を低下さ
せたジストレーエミッション源トなって管の特性を害す
ることになる。
Furthermore, the high evaporation of barium causes barium to adhere to adjacent electrode components, becoming a source of stray emissions that reduce electrode insulation deterioration and impairing tube properties.

この発明はこれら従来の欠点を解消するためになされた
もので、二つの電子放射物質層の間に透孔を備えたバリ
ア層を設けることによシ、エミッション寿命特性を改曽
するとともに、管の絶縁劣化等を生じない陰極を提供す
ることを目的としている。
This invention was made to eliminate these conventional drawbacks, and by providing a barrier layer with holes between two electron-emitting material layers, it not only improves the emission lifetime characteristics but also improves the tube efficiency. The purpose is to provide a cathode that does not cause insulation deterioration or the like.

以下、この発明の実施例を第2図を参照しながら詳述す
る。第2図において、(2)は還元元素として0.05
重量パーセントのマグネシウムおよびシリコンを含む厚
さ0.11 mnのニッケルからなる基体金Jfi、(
3)はバリウム、ストロンチウム、カルシウムの三元酸
化物に0.1重量パーセントのジルコニウムを混合した
粉末からなる厚さ0.06mの冗子放射物質第−ffl
、(4)はバリウム、ストロンチウム、カルシウムの三
元酸化物の粉末よシなる厚さ0.04門の電子放射物質
第二層、(ロ)は500人程鹿の厚みを有するニッケル
からなるバリア層である。バリアJ(’70乃は電子放
射物質第一層(3) 、 M二ffV (4)の間に設
けられ、1個あるいは複数個の透孔a3を有する薄膜で
ある。
Hereinafter, embodiments of the present invention will be described in detail with reference to FIG. In Figure 2, (2) is 0.05 as a reducing element.
Substrate gold Jfi, consisting of 0.11 mn thick nickel containing weight percent magnesium and silicon (
3) is a 0.06 m thick radioactive material consisting of a powder of ternary oxides of barium, strontium, and calcium mixed with 0.1% by weight of zirconium.
, (4) is a second layer of electron-emitting material made of powder of ternary oxides of barium, strontium, and calcium with a thickness of 0.04 mm, and (b) is a barrier made of nickel with a thickness of about 500 deer. It is a layer. Barrier J ('70) is a thin film provided between the first layer of electron emitting material (3) and the second layer of MffV (4) and having one or more through holes a3.

バリア層(6)は、通常のスプレー法により基体金属(
2)の上に被着された三元酸化物の出発物質であるバリ
ウム、ストロンチウム、カルシウムの三元炭酸塩と水素
化ジルコニウムの混合物の上に、ニッケルを真空蒸着す
ることによって得られる。
The barrier layer (6) is coated with the base metal (
2) is obtained by vacuum evaporation of nickel onto a mixture of ternary carbonates of barium, strontium, calcium and zirconium hydride, which are the starting materials for the ternary oxide deposited on 2).

500人程鹿の厚みの蒸M膜の場合、多数の透孔を有し
ている。バリア層(財)を設けた後、バリア層(財)の
上に通常のスプレー法によシミ子放射物質第二居(4)
の出発物質であるバリウム、ストロンチウム、カルシウ
ムの三元炭a塩を積層塗布して陰+fi (1)を形成
する。その後上記陰極(ロ)は電子銃の一部品として組
立てられ、電子管製造における周知の排気9分解、陰極
の活性化処理が施されて電子放射機能が具備される。
In the case of a vaporized M film with a thickness of about 500 deer, it has many through holes. After providing the barrier layer (material), apply the second stain emitter (4) on top of the barrier layer (material) using the usual spray method.
The ternary carbon a salts of barium, strontium, and calcium, which are the starting materials, are coated in a layered manner to form the shade +fi (1). Thereafter, the cathode (b) is assembled as a part of an electron gun, and subjected to the well-known evacuation process and cathode activation process in electron tube manufacturing to provide an electron emission function.

前記の(1) 、 (2)式等の反応によシ生じた遊に
バリウムは、ヒータ(5)による加熱によって電子放射
物質第一層(3)よシミ子放射物質第二唐(4)の方向
へ拡散移動するが、バリア1301)によル拡散は制限
を受け、電子放射物質第二n(4)へは透孔(1?1を
通してのみ供給される。との透孔01の大きさおよび数
は取シ出し電流穴等の使用条件を考慮して適宜決定し得
る。透孔α場を通過した遊離バリウムは電子放射物質第
二層(4)表面に達し、電子放射に寄与する。
The free barium generated by the reactions of formulas (1) and (2) above is heated by the heater (5) to form the first layer of electron emitting material (3) and the second layer of simulator emitting material (4). However, the diffusion is restricted by the barrier 1301), and the electron emitting material 2nd n(4) is supplied only through the through hole (1?1). The size and number can be determined as appropriate in consideration of the usage conditions such as the current extraction hole, etc. The free barium that has passed through the through-hole α field reaches the surface of the second layer of electron emitting material (4) and contributes to electron emission. .

このように、バリア層に)の存在にあシネ所望の遊離バ
リウムの拡散、蒸発による消耗量が激減し、長期にわた
って安定した電子放射を得ることができる。また、バリ
ウムの付着による電極同絶縁劣化等の特性低下も生じな
い。
Thus, due to the presence of the barrier layer), the amount of free barium consumed due to diffusion and evaporation is drastically reduced, and stable electron emission can be obtained over a long period of time. Further, properties such as deterioration of electrode insulation due to adhesion of barium do not occur.

t43図は電子放射の寿命特性を表わすグフフである。The t43 diagram is a guffaw representing the lifetime characteristics of electron radiation.

突栓aで示すこの発明による陰極(均を実装した受像管
の場合、破線すで示す従来の陰極(1)を実装した受像
管の場合に比べて寿命特性が著しく改善されていること
がわかる。
It can be seen that in the case of the picture tube equipped with the cathode (uniform) according to the present invention shown by the protruding plug a, the life characteristics are significantly improved compared to the case of the picture tube mounted with the conventional cathode (1) shown by the broken line. .

なお上記実施例においては、バリア層θ枠を形成する金
属としてニッケルを用いたが、(Ba 、 Sr 。
In the above example, nickel was used as the metal forming the barrier layer θ frame, but (Ba, Sr).

0a)Oとの還元反応が生じ難い高融点金属群、たとえ
ばコバ/l/)、プフチナ、モリブデン、白金等を随意
に選ぶことが可能である。またバリア烈(J5’Jは上
記実施例では一層のみとしたが、¥5数層であっても同
じ作用効果を呈することは勿論のことである。
0a) It is possible to arbitrarily select a group of high-melting point metals that are unlikely to undergo a reduction reaction with O, such as Koba/l/), Puchina, molybdenum, platinum, and the like. Further, although only one layer of barrier layer (J5'J) was used in the above embodiment, it goes without saying that the same effect can be obtained even with several layers.

以上のように、この発明によれば、透孔を有するバリア
を設けるだけの簡単な手段によシエミッション寿命を改
善でき、長期にわたって安定した電子放射を行なうとと
もに、電子管の特性低下をもたらさない陰極を得ること
ができる。
As described above, according to the present invention, the emission life can be improved by simply providing a barrier having through holes, and a cathode that emits electrons stably over a long period of time and does not cause deterioration in the characteristics of the electron tube can be obtained. can be obtained.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は従来の陰極の要部断面図、第2図はこの発明の
陰極の実施例を示す要部断面図、第3図は従来の陰極と
この発明の陰はの寿命特性を比駿して示したグラフであ
る。 (2)・・・基体金属、(3)・・・電子放射物質第二
層、(4)・・・電子放射物質第二層、(財)・・・バ
リアノアη、(1枠・・・透孔。 なお、図中同一符号は同一または相当部分を示す。 代理人、葛野信−(外1名)
Fig. 1 is a cross-sectional view of the main part of a conventional cathode, Fig. 2 is a cross-sectional view of the main part showing an embodiment of the cathode of the present invention, and Fig. 3 is a comparison of the life characteristics of the conventional cathode and the cathode of the present invention. This is a graph shown as follows. (2)...Base metal, (3)...Second layer of electron emitting material, (4)...Second layer of electron emitting material, (Foundation)...Barrier η, (1 frame... Through hole. In addition, the same reference numerals in the drawings indicate the same or corresponding parts. Agent: Makoto Kuzuno (1 other person)

Claims (1)

【特許請求の範囲】[Claims] (1)微量の還元性元素を含有する基体金IFへと、こ
の基体金属上に被着された電子放射物質第一層と、この
電子放射物質第一層に積層して設けられる電子放射物質
第二層とを備え、前記電子数WJ物質第一層はアルカリ
土類金属の単種または複数種の酸化物に微量の亘元性元
素を混合した粉末からなり、前記電子放射物質第二層は
アルカリ土類金属の単種または複数種の酸化物粉末から
なる陰極において、前記電子放射物質第一層と電子放射
物質第二層との間に単数まだは複数個の透孔を有する高
融点金属より選定された薄膜状のバリア層を設けたこと
を特徴とする陰極。
(1) A first layer of electron emitting material deposited on the base metal IF containing a trace amount of reducing element, and an electron emitting material provided in a layered manner on the first layer of electron emitting material. The first layer of the electron number WJ material is made of a powder of a single or multiple oxide of an alkaline earth metal mixed with a trace amount of a universal element, and the second layer of the electron emitting material is a cathode made of oxide powder of one or more kinds of alkaline earth metals, with a high melting point having one or more through holes between the first layer of electron emitting material and the second layer of electron emitting material. A cathode characterized by having a thin film barrier layer selected from metal.
JP57215751A 1982-12-07 1982-12-07 Cathode Pending JPS59105234A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57215751A JPS59105234A (en) 1982-12-07 1982-12-07 Cathode

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57215751A JPS59105234A (en) 1982-12-07 1982-12-07 Cathode

Publications (1)

Publication Number Publication Date
JPS59105234A true JPS59105234A (en) 1984-06-18

Family

ID=16677610

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57215751A Pending JPS59105234A (en) 1982-12-07 1982-12-07 Cathode

Country Status (1)

Country Link
JP (1) JPS59105234A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4904896A (en) * 1984-11-27 1990-02-27 Rca Licensing Corporation Vacuum electron tube having an oxide cathode comprising chromium reducing agent

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4904896A (en) * 1984-11-27 1990-02-27 Rca Licensing Corporation Vacuum electron tube having an oxide cathode comprising chromium reducing agent

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