JPS6054734B2 - thermionic emission cathode - Google Patents
thermionic emission cathodeInfo
- Publication number
- JPS6054734B2 JPS6054734B2 JP52116868A JP11686877A JPS6054734B2 JP S6054734 B2 JPS6054734 B2 JP S6054734B2 JP 52116868 A JP52116868 A JP 52116868A JP 11686877 A JP11686877 A JP 11686877A JP S6054734 B2 JPS6054734 B2 JP S6054734B2
- Authority
- JP
- Japan
- Prior art keywords
- boride
- cathode
- layer
- deposited
- vapor
- 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.)
- Expired
Links
- 229910052751 metal Inorganic materials 0.000 claims description 24
- 239000002184 metal Substances 0.000 claims description 24
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 6
- 229910052791 calcium Inorganic materials 0.000 claims description 6
- 239000011575 calcium Substances 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- 229910052721 tungsten Inorganic materials 0.000 claims description 4
- 150000002739 metals Chemical class 0.000 claims description 3
- 239000010955 niobium Substances 0.000 claims description 3
- 229910003468 tantalcarbide Inorganic materials 0.000 claims description 3
- 229910052715 tantalum Inorganic materials 0.000 claims description 3
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims description 3
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 3
- 239000010937 tungsten Substances 0.000 claims description 3
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 2
- 229910026551 ZrC Inorganic materials 0.000 claims description 2
- LRTTZMZPZHBOPO-UHFFFAOYSA-N [B].[B].[Hf] Chemical compound [B].[B].[Hf] LRTTZMZPZHBOPO-UHFFFAOYSA-N 0.000 claims description 2
- OTCHGXYCWNXDOA-UHFFFAOYSA-N [C].[Zr] Chemical compound [C].[Zr] OTCHGXYCWNXDOA-UHFFFAOYSA-N 0.000 claims description 2
- VDZMENNHPJNJPP-UHFFFAOYSA-N boranylidyneniobium Chemical compound [Nb]#B VDZMENNHPJNJPP-UHFFFAOYSA-N 0.000 claims description 2
- XTDAIYZKROTZLD-UHFFFAOYSA-N boranylidynetantalum Chemical compound [Ta]#B XTDAIYZKROTZLD-UHFFFAOYSA-N 0.000 claims description 2
- 238000005304 joining Methods 0.000 claims description 2
- 238000010030 laminating Methods 0.000 claims description 2
- NFFIWVVINABMKP-UHFFFAOYSA-N methylidynetantalum Chemical compound [Ta]#C NFFIWVVINABMKP-UHFFFAOYSA-N 0.000 claims description 2
- 229910052750 molybdenum Inorganic materials 0.000 claims description 2
- 239000011733 molybdenum Substances 0.000 claims description 2
- 229910052758 niobium Inorganic materials 0.000 claims description 2
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 claims description 2
- MZLGASXMSKOWSE-UHFFFAOYSA-N tantalum nitride Chemical compound [Ta]#N MZLGASXMSKOWSE-UHFFFAOYSA-N 0.000 claims description 2
- 229910052726 zirconium Inorganic materials 0.000 claims description 2
- ZVWKZXLXHLZXLS-UHFFFAOYSA-N zirconium nitride Chemical compound [Zr]#N ZVWKZXLXHLZXLS-UHFFFAOYSA-N 0.000 claims description 2
- 150000004767 nitrides Chemical class 0.000 claims 1
- 238000004544 sputter deposition Methods 0.000 description 19
- 238000006243 chemical reaction Methods 0.000 description 9
- 239000013078 crystal Substances 0.000 description 9
- 230000004888 barrier function Effects 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 229910025794 LaB6 Inorganic materials 0.000 description 6
- 239000000758 substrate Substances 0.000 description 6
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 238000007740 vapor deposition Methods 0.000 description 4
- 229910004533 TaB2 Inorganic materials 0.000 description 3
- 229910052786 argon Inorganic materials 0.000 description 3
- 239000010408 film Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000003466 welding Methods 0.000 description 3
- 239000000020 Nitrocellulose Substances 0.000 description 2
- -1 ZrNl Chemical compound 0.000 description 2
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 2
- 239000012300 argon atmosphere Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- 238000001552 radio frequency sputter deposition Methods 0.000 description 2
- 239000003870 refractory metal Substances 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- QYEXBYZXHDUPRC-UHFFFAOYSA-N B#[Ti]#B Chemical compound B#[Ti]#B QYEXBYZXHDUPRC-UHFFFAOYSA-N 0.000 description 1
- 229910052693 Europium Inorganic materials 0.000 description 1
- 229910052688 Gadolinium Inorganic materials 0.000 description 1
- 229910003862 HfB2 Inorganic materials 0.000 description 1
- 229910019742 NbB2 Inorganic materials 0.000 description 1
- 229910033181 TiB2 Inorganic materials 0.000 description 1
- 229910007948 ZrB2 Inorganic materials 0.000 description 1
- DBNPLCUZNLSUCT-UHFFFAOYSA-N [B].[B].[B].[B].[B].[B].[Ba] Chemical compound [B].[B].[B].[B].[B].[B].[Ba] DBNPLCUZNLSUCT-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- VWZIXVXBCBBRGP-UHFFFAOYSA-N boron;zirconium Chemical compound B#[Zr]#B VWZIXVXBCBBRGP-UHFFFAOYSA-N 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- OGPBJKLSAFTDLK-UHFFFAOYSA-N europium atom Chemical compound [Eu] OGPBJKLSAFTDLK-UHFFFAOYSA-N 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- UIWYJDYFSGRHKR-UHFFFAOYSA-N gadolinium atom Chemical compound [Gd] UIWYJDYFSGRHKR-UHFFFAOYSA-N 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Solid Thermionic Cathode (AREA)
Description
【発明の詳細な説明】
本発明は、熱電子放射陰極、特に六硼化カルシウム型構
造を有する硼化物を主材料とする熱電子放射陰極に関す
るものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a thermionic-emitting cathode, particularly a thermionic-emitting cathode whose main material is a boride having a calcium hexaboride type structure.
六硼化ランタンLaB6に代表される六硼化カルシウム
型構造を有する硼化物は、仕事関数が小さ゛一龜叡−゛
゛』に^ものが一般的に使用されている。Borides having a calcium hexaboride type structure, such as lanthanum hexaboride LaB6, have a small work function and are generally used.
しかし、この熱電子放射陰極チップを高温下で作動させ
た場合、通常の支持金属であるタングステン、タンタル
などと化学反応を起し、熱電子放射陰極のチップ風化し
たり、支持金属が脆化するなど長時間安定に作動させる
ことが困難であつた。However, when this thermionic-emitting cathode chip is operated at high temperatures, a chemical reaction occurs with normal supporting metals such as tungsten and tantalum, causing weathering of the thermionic-emitting cathode chip and embrittlement of the supporting metal. It was difficult to operate stably for long periods of time.
この困難を解決するために、加熱用構体を熱電子放射陰
極チップと接触せずに、熱電子放射陰極チップの支持は
冷却器を備えた構体によつて実現し、もつて化学反応を
阻止する提案(特公昭45−40576)があるが、こ
のような提案では、構造が複雑であり、しかも、熱電子
放射陰極が通常使用される個所、例えば電子顕微鏡陰極
、電子管陰極などでは加熱時の電力は小さく10ワット
以下が普通である。従つて上記のような構造では加熱電
力が大きすぎるという欠点があつた。本発明はこれらの
欠点を解決したすぐれた熱電子放射陰極を提供しようと
するものである。To overcome this difficulty, the heating structure does not come into contact with the thermionic-emitting cathode chip, and the support of the thermionic-emitting cathode chip is realized by a structure equipped with a cooler, thereby preventing the chemical reaction. There is a proposal (Japanese Patent Publication No. 45-40576), but such a proposal would have a complicated structure, and in places where a thermionic emission cathode is normally used, such as an electron microscope cathode or an electron tube cathode, the power consumption during heating would be too low. is small, usually less than 10 watts. Therefore, the above structure has the disadvantage that the heating power is too large. The present invention aims to provide an excellent thermionic emission cathode that solves these drawbacks.
すなわち、本発明は六硼化カルシウム型構造を有する硼
化物チップを用いた熱電子放射陰極のにおいて、前記チ
ップの一端にこれと反応し難い物質の蒸着層、反応し難
い物質と支持金属との混合物の蒸着層及び支持金属蒸着
層を積層し、さらに支持金属の蒸着層と電極とを支持金
属線を介して接合してなる熱電子放射陰極である。以下
さらに詳しく本発明を説明する。That is, the present invention provides a thermionic emission cathode using a boride chip having a calcium hexaboride type structure, in which a vapor deposited layer of a substance that is difficult to react with the cathode is formed on one end of the chip, and a layer of a material that is difficult to react with the cathode is formed between the substance that is difficult to react with the cathode and a supporting metal. This is a thermionic emission cathode formed by laminating a vapor-deposited layer of a mixture and a vapor-deposited supporting metal layer, and further joining the vapor-deposited supporting metal layer and an electrode via a supporting metal wire. The present invention will be explained in more detail below.
本発明は前記したように六硼化カルシウム型構造を有す
る硼化物(以下硼化物という)チップの一端にこれと反
応し難い物質蒸着層(以下反応障壁層という)支持金属
蒸着層(以下支持金属層という)との間に、これらの混
合物からなる蒸着層(以下混合物層という)を設けたこ
とを特徴とするもので、硼化物チップの一端に均一で密
着性にすぐれた層が、積層され、しかも混合物層がある
ため熱サイクルを100(0]以上受けても熱陰極にク
ラックを生じたりすることはなく、加熱効率にすぐれた
ものである。As described above, the present invention provides a support metal vapor deposition layer (hereinafter referred to as a support metal) on one end of a boride (hereinafter referred to as boride) chip having a calcium hexaboride type structure, a vapor deposited layer of a substance that does not easily react with the boride (hereinafter referred to as a reaction barrier layer), and a support metal deposited layer (hereinafter referred to as a reaction barrier layer). The feature is that a vapor deposited layer (hereinafter referred to as a mixture layer) made of a mixture of these is provided between the boride chip and the boride chip. Moreover, since there is a mixture layer, the hot cathode does not crack even when subjected to thermal cycles of 100(0) or more, and has excellent heating efficiency.
これを図面に従つて説明すると、第1図は、六硼化カル
シウム型構造を有する硼化物チップの一端に反応障壁層
、支持金属層を蒸着した熱電子放射材料の断面図である
。To explain this according to the drawings, FIG. 1 is a cross-sectional view of a thermionic emission material in which a reaction barrier layer and a supporting metal layer are deposited on one end of a boride chip having a calcium hexaboride type structure.
1は、硼化物チップ、2は反応障壁層、3は混合物層、
4は支持金属層である。1 is a boride chip, 2 is a reaction barrier layer, 3 is a mixture layer,
4 is a supporting metal layer.
また第2図は、本発明品の使用例を示した説明図であつ
て、熱電子放射陰極チップに前記各層をスパッタリング
法により蒸着した後、支持金属層と電極とを支持金属線
を介して接合して電極を支持台に取付けたものである。FIG. 2 is an explanatory diagram showing an example of the use of the product of the present invention, in which the above-mentioned layers are deposited on a thermionic emission cathode chip by sputtering, and then the supporting metal layer and the electrode are connected via a supporting metal wire. The electrodes are attached to a support base.
5はセラミック支持台を示し、6は電極、7は支持金属
線である。第1図に示したような熱電子放射陰極チップ
を、第2図のように熱電子放射陰極として使用すること
ができる。障壁層のターゲットとしては、硼化物及び支
持金属と反応し難く、1900C以上の融点を持ち、か
つ1600′Cにおける平衡蒸気圧が10−5T0rr
以のものであれば、全て使用可能であ一るが、硼化物で
は、硼化ニオブNbB2、硼化ジルコニウムZrB2、
硼化ハフニウムHfB2、硼化タンタルTaB2、炭化
物では、炭化タンタルTaC、炭化ジルコニウムZrc
l窒化物では窒化ジルコニウムZrNl窒化タンタルT
aNなどが特に好ましい。.又、支持金属のターゲット
としては、タンタルTalタングステンW1ニオブNb
lモリブデンMOなどが特に好ましい。次にスパッタリ
ング法により蒸着層の形成させるには一般的に不活性雰
囲気下グロー放電によソー行われる。5 is a ceramic support base, 6 is an electrode, and 7 is a support metal wire. A thermionic emitting cathode chip as shown in FIG. 1 can be used as a thermionic emitting cathode as shown in FIG. Targets for the barrier layer include materials that are difficult to react with borides and supporting metals, have a melting point of 1900C or higher, and have an equilibrium vapor pressure of 10-5T0rr at 1600'C.
Any of the following can be used, but among borides, niobium boride NbB2, zirconium boride ZrB2,
Hafnium boride HfB2, tantalum boride TaB2, carbides include tantalum carbide TaC, zirconium carbide Zrc
lNitrides include zirconium nitride, ZrNl, tantalum nitride, and T.
Particularly preferred is aN. .. In addition, as supporting metal targets, tantalum, Tal, tungsten, W1, niobium, Nb
Particularly preferred is molybdenum MO. Next, forming a deposited layer by sputtering is generally performed by glow discharge under an inert atmosphere.
スパッタリング法には直卯χスパッタ装置と高周波RF
スパッタ装置を用いる方法がある。■スパッタ装置は真
空槽内にターゲットと基板とを対向するように配置し、
陰極はターゲット、陽極は基板ホールダーとし、電極間
に数KVの直流電圧を印加すると、電極間にグロー放電
が発生するようにしたものから構成されている。グロー
放電すると放電空間にアルゴンプラズマが形成され、プ
ラズマ中のアルゴンイオンが陰極電位降下で加速されタ
ーゲット陰極表面に衝突し、ターゲット表面をスパッタ
蒸発させる。The sputtering method uses a straight chi sputtering device and high frequency RF.
There is a method using a sputtering device. ■The sputtering equipment is placed in a vacuum chamber with the target and substrate facing each other.
The cathode is a target, the anode is a substrate holder, and when a DC voltage of several kilovolts is applied between the electrodes, a glow discharge is generated between the electrodes. When the glow discharge occurs, argon plasma is formed in the discharge space, and argon ions in the plasma are accelerated by the cathode potential drop and collide with the target cathode surface, sputtering and vaporizing the target surface.
このようにして蒸発したスパッタ粒子が対向して置かれ
た基板上に沈着して薄膜が形成される。導電性のターゲ
ットを用いない場合はxスパッタ装置で十分であるが導
電性のターゲットでない場合はRFスパッタ装置を用い
る。RFスパッタ装置はスパッタ入射イオンとなる10
−21′0rr程度の不活性ガス(Arガス)をスパッ
タ室内に導入し、ターゲット電極とアースされたスパッ
タ空間に数KVの高周波(13.56MH2)を印加す
ると、スパッタ室内にグロー放電が発生するように構成
されている。グロー放電で発生したプラズマ中の電子と
Ar+イオンが印加した高周波電圧によりターゲットに
交互に衝突する。高周波放電においては、電子が高周波
電界により電極間を往復するため衝突電離が効果的に行
われる。The sputtered particles evaporated in this way are deposited on the opposing substrates to form a thin film. If a conductive target is not used, an x sputtering device is sufficient, but if a conductive target is not used, an RF sputtering device is used. The RF sputtering equipment becomes sputtering incident ions10
When an inert gas (Ar gas) of about -21'0rr is introduced into the sputtering chamber and a high frequency of several KV (13.56MH2) is applied to the sputtering space that is grounded to the target electrode, glow discharge occurs in the sputtering chamber. It is configured as follows. Electrons and Ar+ ions in the plasma generated by the glow discharge alternately collide with the target due to the applied high frequency voltage. In high-frequency discharge, impact ionization is effectively performed because electrons travel back and forth between electrodes due to the high-frequency electric field.
蒸着開始にあたつてはまずアルゴンガスで基材表面をス
パッターすると基材の表面がクリーニングされ、密着性
が良好となる。When starting vapor deposition, first sputtering the surface of the substrate with argon gas cleans the surface of the substrate and improves adhesion.
さらに反応障壁層と支持金属層との間に生じる熱膨張率
の差による歪応力は、中間に反応障壁材料と支持金属材
料とを同時にスパッタリング蒸着することにより緩和す
ることができる。実施例では、HB6単結晶について説
明するが、本発明の方法は、他の硼化物、例えば硼化バ
リウム、硼化イットリウム、硼化ユーロピウム、硼化ガ
ドリニウムなどの六硼化物単結晶熱電子放射陰極にも適
用できる。Furthermore, the strain stress caused by the difference in thermal expansion coefficient between the reaction barrier layer and the supporting metal layer can be alleviated by simultaneously depositing the reaction barrier material and the supporting metal material in the middle by sputtering. Although the examples describe HB6 single crystals, the method of the present invention can be applied to other borides, such as hexaboride single crystal thermionic emitting cathodes such as barium boride, yttrium boride, europium boride, and gadolinium boride. It can also be applied to
又、ホットブレス法等により成型した多結晶焼結体の熱
電子放射陰極にも適用できる。以下実施例によつて本発
明を説明する。It can also be applied to a thermionic emitting cathode made of a polycrystalline sintered body formed by a hot-breathing method or the like. The present invention will be explained below with reference to Examples.
実施例1
TaNおよびTaをスパッターターゲットとし、3×1
0−3T0rrのアルゴン雰囲気中、加速電圧5KVの
条件で、スパッター蒸着を行なつた。Example 1 TaN and Ta are used as sputter targets, 3×1
Sputter deposition was carried out in an argon atmosphere of 0-3T0rr under conditions of an accelerating voltage of 5KV.
被スパッター物質はLaB8単結晶チップであり、該チ
ノブの先端は熱電子放射材料として使用するため蒸着物
が付着しないようにアルミ箔で覆つた。まず最初にTa
N3紛間スパッタ蒸着し、厚さ50μの膜とし、次の3
紛間では、Ta<!:.TaNを共にスパッター蒸着し
、厚さ50μの膜とした。次にTaだけのスパッター蒸
着をさらに3紛間行ない厚さ50μの膜を形成した。得
られた熱陰極をスポット溶接によりW線と結合し、5刈
0−5T0rrの真空下でLaBe,単結晶チップ先端
の温度が1600℃、50CJIi!f間加熱したがF
B,単結晶部分には何の変化も見られなかつた。The material to be sputtered was a LaB8 single crystal chip, and the tip of the chinobu was covered with aluminum foil to prevent deposits from adhering to it because it was used as a thermionic emission material. First of all, Ta
N3 powder was sputter deposited to form a film with a thickness of 50μ, and the following 3
In the confusion, Ta<! :. TaN was also sputter deposited to form a 50μ thick film. Next, sputter deposition of only Ta was performed three more times to form a film with a thickness of 50 μm. The obtained hot cathode was joined to the W wire by spot welding, and the temperature at the tip of the single crystal tip was 1600°C and 50CJIi! under a vacuum of 0-5T0rr. Although it was heated for f
B: No change was observed in the single crystal part.
比較のために特願昭52−116864号(特公昭関一
26766号公報)の実施例1で作成した陰極と実施例
1で作成した陰極の熱サイクル試験を行つた。その結果
を表に示す。熱サイクル試験は温度1600℃で1時間
加熱し冷却後常温で3紛間放置の繰り返しを行つた。な
お比較例の熱陰極の製法は次のとおりである。For comparison, a thermal cycle test was conducted on the cathode prepared in Example 1 of Japanese Patent Application No. 52-116864 (Japanese Patent Publication No. 116864/1983) and the cathode prepared in Example 1. The results are shown in the table. The thermal cycle test was repeated by heating at 1600° C. for 1 hour, cooling, and then leaving at room temperature for 3 times. The method for manufacturing the hot cathode of the comparative example is as follows.
LaB6からなるチップ下部側面に、反応障壁層を形成
するTiB2粉末、硝酸セルロール及びブタノールから
なるペーストを約60ミクロンの厚さに塗布被覆し、こ
れを充分乾燥後、さらにその上に難融性金属層を形成す
るW粉末と硝酸セルロース及びブタノールからなるペー
ストを約40ミクロンの厚さに塗布した。A paste consisting of TiB2 powder, cellulose nitrate, and butanol to form a reaction barrier layer is coated on the lower side surface of the chip made of LaB6 to a thickness of about 60 microns, and after it is sufficiently dried, a refractory metal is further applied on top of it. A paste consisting of W powder, cellulose nitrate and butanol forming a layer was applied to a thickness of about 40 microns.
このチップをアルゴン雰囲気中で、温度1800Cで1
紛間焼結して焼付けた。得られた三層構造を側面にもつ
LaB6チップの難融性金属層の上に、支持金属として
w線をスポット溶接により接合固定し、LlB6陰極と
した。実施例2スパッターターゲットとして、TaB,
とWを使用し、実施例1と同じ条件で、LaB6単結晶
上にスパッター蒸着を行なつた。This chip was heated at 1800C in an argon atmosphere for 1
Sintered and baked. On the refractory metal layer of the LaB6 chip having the obtained three-layer structure on its side surface, a W wire was bonded and fixed as a supporting metal by spot welding to form an LlB6 cathode. Example 2 As a sputter target, TaB,
Sputter deposition was performed on a LaB6 single crystal under the same conditions as in Example 1 using and W.
すなわち、LaB6単結晶に直接TaB2を30分間ス
パッター蒸着(厚さ50μ)し、次に30分間TaB2
とWとをそれぞれ1:1の割合となるように同時に蒸着
(厚さ50μ)した。次にWだけのスパッター蒸着を3
紛間実施した。こうして得られた陰極をスポット溶接に
よりTa線と結合し、3×10−5T0rrの真空下で
、LaB6単結晶チップ先端温度が1700℃になるよ
うに308間加熱した後、急冷して常温とし、すぐに又
加熱するサイクルを100徊繰り返したがLlB6単結
晶部分には何の変化もなかつた。本発明品は、小電力で
作動し、長寿命てあり、かつ電子放射特性に優れ、冷却
、加熱に強い熱電子放射陰極を得ることができる。スパ
ッタリング法による蒸着では、通常の真空蒸着と比較し
て基材への密着性が極めて良好て緻密な薄膜が形成され
る。That is, TaB2 was directly sputter deposited on the LaB6 single crystal for 30 minutes (thickness 50μ), and then TaB2 was deposited for 30 minutes.
and W were simultaneously deposited (thickness: 50 μm) at a ratio of 1:1. Next, sputter deposition of only W is performed 3 times.
It was carried out in the interim. The cathode thus obtained was bonded to a Ta wire by spot welding, heated under a vacuum of 3 x 10-5 T0rr for 308 minutes so that the tip temperature of the LaB6 single crystal tip reached 1700°C, and then rapidly cooled to room temperature. Immediately, the heating cycle was repeated 100 times, but there was no change in the LlB6 single crystal portion. The product of the present invention can provide a thermionic emission cathode that operates with low power, has a long life, has excellent electron emission characteristics, and is resistant to cooling and heating. Vapor deposition by sputtering forms a dense thin film with extremely good adhesion to the substrate compared to normal vacuum vapor deposition.
第1図は本発明の実施例の熱電子放射陰極チップの断面
図;第2図は本発明品の説明図である。FIG. 1 is a sectional view of a thermionic emitting cathode chip according to an embodiment of the present invention; FIG. 2 is an explanatory diagram of the product of the present invention.
Claims (1)
いた熱電子放射陰極において、前記チップの一端にこれ
と反応し難い物質の蒸着層、反応し難い物質と支持金属
との混合物の蒸着層及び支持金属蒸着層を積層し、さら
に支持金属の蒸着層と電極とを支持金属線を介して接合
してなる熱電子放射陰極。 2 反応し難い物質が硼化ニオブ、硼化ジルコニウム、
硼化ハハフニウム、硼化タンタル、から撰ばれた硼化物
、炭化タンタル、炭化ジルコニウムから撰ばれた炭化物
、窒化ジルコニウム、窒化タンタルから撰ばれた窒化物
である特許請求の範囲第1項記載の熱電子放射陰極。 3 支持金属がタンタル、タングステン、ニオブ、モリ
ブデンから撰ばれた1種以上上の金属である特許請求の
範囲第1項記載の熱電子放射陰極。[Claims] 1. In a thermionic emission cathode using a boride chip having a calcium hexaboride type structure, at one end of the chip there is a vapor deposited layer of a substance that does not easily react with the boride, and a layer of a substance that does not easily react with the boride and a support metal. A thermionic emission cathode formed by laminating a vapor-deposited layer of a mixture of the above and a vapor-deposited supporting metal layer, and further joining the vapor-deposited supporting metal layer and an electrode via a supporting metal wire. 2 Substances that are difficult to react with are niobium boride, zirconium boride,
The thermoelectron according to claim 1, which is hafnium boride, tantalum boride, a boride selected from tantalum carbide, a carbide selected from zirconium carbide, zirconium nitride, and a nitride selected from tantalum nitride. Emitting cathode. 3. The thermionic emitting cathode according to claim 1, wherein the supporting metal is one or more metals selected from tantalum, tungsten, niobium, and molybdenum.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP52116868A JPS6054734B2 (en) | 1977-09-30 | 1977-09-30 | thermionic emission cathode |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP52116868A JPS6054734B2 (en) | 1977-09-30 | 1977-09-30 | thermionic emission cathode |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5451464A JPS5451464A (en) | 1979-04-23 |
| JPS6054734B2 true JPS6054734B2 (en) | 1985-12-02 |
Family
ID=14697609
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP52116868A Expired JPS6054734B2 (en) | 1977-09-30 | 1977-09-30 | thermionic emission cathode |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6054734B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58225527A (en) * | 1982-06-24 | 1983-12-27 | Denki Kagaku Kogyo Kk | Hot cathode and manufacturing method thereof |
-
1977
- 1977-09-30 JP JP52116868A patent/JPS6054734B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5451464A (en) | 1979-04-23 |
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