JPH0618109B2 - Liquid metal ion source cleaning method - Google Patents
Liquid metal ion source cleaning methodInfo
- Publication number
- JPH0618109B2 JPH0618109B2 JP62204254A JP20425487A JPH0618109B2 JP H0618109 B2 JPH0618109 B2 JP H0618109B2 JP 62204254 A JP62204254 A JP 62204254A JP 20425487 A JP20425487 A JP 20425487A JP H0618109 B2 JPH0618109 B2 JP H0618109B2
- Authority
- JP
- Japan
- Prior art keywords
- emitter
- ion source
- liquid metal
- metal ion
- lmis
- 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 - Lifetime
Links
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- Electron Sources, Ion Sources (AREA)
Description
【発明の詳細な説明】 (産業上の利用分野) この発明は、集束イオンビームによるイオン注入装置に
用いる液体金属イオン源を洗浄化方法に関するものであ
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for cleaning a liquid metal ion source used in an ion implantation apparatus using a focused ion beam.
(従来の技術) 半導体素子の集積化、微細化に伴い、集束イオンビーム
(Focused Ion Beam;以下FIBという)技術が注目を集
めている。この技術はマスクなしで、かつミクロン(μ
m)以下のオーダーの領域で、ミリング、エッチング、
レジスト露光、インオ注入が行なえるので微細加工技術
として極めて重要である。上記の方法で微細加工を行な
うには液体金属イオン源(Liquid Metal Ion Source;
以下LMISという)が必要不可欠であり、これをFIB装置
に搭載してマイクロビームを形成する。(Prior Art) Focused ion beam (FIB) technology has been attracting attention as semiconductor elements are integrated and miniaturized. This technology is maskless and micron (μ
m) Milling, etching,
It is extremely important as a microfabrication technology because it can perform resist exposure and implantation. Liquid metal ion source (Liquid Metal Ion Source;
(Hereinafter referred to as LMIS) is indispensable and is mounted on the FIB device to form a microbeam.
従来、LMIS材料として、文献、マイクロエレクトロニク
ス−ホトニクス,マテリアルズ,センサーズアンドテク
ノロジー(Microelectronics-Photonics,Materials,Sen
sors and Technology)Vol.10.p21に記載の如く、比較
的安定した動作イオン電流を供給することができる、Ga
(ガリウム),Au(金)−Si(シリコン),Au(金)−
Si(シリコン)−Be(ベリリウム)が広く用いられてき
た。Conventionally, as LMIS materials, literature, microelectronics-photonics, materials, sensors and technology (Microelectronics-Photonics, Materials, Sen
sors and Technology) Vol.10.p21, it can supply a relatively stable operating ion current, Ga
(Gallium), Au (gold) -Si (silicon), Au (gold)-
Si (silicon) -Be (beryllium) has been widely used.
(発明が解決しよとする問題点) しかしながら上記のGa,Au−Si,Au−Si−BeのLMISにお
いてもイオン源動作時に、スパッタリング原子によるLM
ISの汚染、あるいは動作中の残留ガスによるLMISの汚染
があり、それによるイオン電流の低下がみられた。特
に、FIB装置のLMIS動作中、エミッタ表面に付着する炭
素が合金のエミッタ表面での流れを悪化させ、それ故FI
Bのイオン電流の低下をひき起すという欠点があった。(Problems to be solved by the invention) However, even in the above LMIS of Ga, Au-Si, and Au-Si-Be, the LM caused by the sputtering atoms is generated during the operation of the ion source.
Contamination of IS or LMIS due to residual gas during operation caused a decrease in ion current. In particular, during LMIS operation of the FIB device, carbon adhering to the emitter surface aggravates the flow of alloy at the emitter surface, and
It had the drawback of causing a decrease in the ionic current of B.
この発明の目的は、安定したFIBのイオン電流を得るこ
とができる液体金属イオン源の洗浄化方法を提供するこ
とにある。An object of the present invention is to provide a method for cleaning a liquid metal ion source capable of obtaining a stable FIB ion current.
(問題点を解決するための手段) この発明は前述した問題点を解決するために、イオン化
すべき金属を溶融保存する溜め部と、エミッタと、引き
出し電極とを有する液体金属イオン源の清浄化方法にお
いて、 水素ガスとアルゴンガスのいずれか一方または両方を前
記液体金属イオン源に供給した後、前記エミッタと前記
引き出し電極との間に電圧を加えて放電を起こし、 この放電により、前記エミッタ表面に付着した炭素を炭
化水素化して揮発させるか、前記エミッタに付着した炭
素をスパッタして除去することを特徴とする。(Means for Solving the Problems) In order to solve the above-mentioned problems, the present invention purifies a liquid metal ion source having a reservoir for melting and storing a metal to be ionized, an emitter, and an extraction electrode. In the method, after supplying one or both of hydrogen gas and argon gas to the liquid metal ion source, a voltage is applied between the emitter and the extraction electrode to cause a discharge, and the discharge causes the surface of the emitter to be discharged. It is characterized in that the carbon attached to the above is converted into a hydrocarbon to be volatilized, or the carbon attached to the emitter is removed by sputtering.
(作用) 以上のように本発明によれば、FIB装置のイオン源部分
に設けられたガス供給手段によりH2ガス及び又はArガス
をLMIS部分に導入すると共にガス排気手段により排気
し、且つLMIS部分に設けられた放電手段によりLMIS部分
を放電させているのでその結果、エミッタ表面に付着し
た炭素は炭化水素(CmHn(m,n=整数))化し、エミ
ッタ表面から揮発する。それ故、エミッタ表面の合金の
流れが改善でき、安定したイオン電流を得ることができ
る。(Operation) As described above, according to the present invention, the H 2 gas and / or the Ar gas is introduced into the LMIS portion by the gas supply means provided in the ion source portion of the FIB device, and is exhausted by the gas exhaust means, and Since the LMIS portion is discharged by the discharge means provided in the portion, as a result, the carbon attached to the emitter surface becomes hydrocarbon (C m H n (m, n = integer)) and volatilizes from the emitter surface. Therefore, the flow of the alloy on the emitter surface can be improved and a stable ion current can be obtained.
(実施例) 第1図〜第3図は本発明の実施例を説明するための図で
あり、以下図面を用いて説明する。第1図はFIB装置の
概略構成図である。1は鏡筒、2はエミッタ、3はイオ
ン化すべき金属を溶融保持する溜め部を兼ねたヒータ
ー、4は引き出し電極、5はレンズ系、6は偏向電極、
7は試料、8はバルブ、9はエミッタ2とヒーター3と
引き出し電極4とで構成されるLMIS部分にガスを供給す
るためのガス導入管、10は加熱電源、11はイオン引
き出し電源、12はイオン加速電源、13はレンズ用電
源、14と15はビーム偏向用電源、16と17は絶縁
端子、18は真空ゲージである。(Embodiment) FIGS. 1 to 3 are views for explaining an embodiment of the present invention, which will be described below with reference to the drawings. FIG. 1 is a schematic configuration diagram of a FIB device. 1 is a lens barrel, 2 is an emitter, 3 is a heater also serving as a reservoir for melting and holding a metal to be ionized, 4 is an extraction electrode, 5 is a lens system, 6 is a deflection electrode,
Reference numeral 7 is a sample, 8 is a valve, 9 is a gas introduction pipe for supplying a gas to the LMIS portion composed of the emitter 2, the heater 3 and the extraction electrode 4, 10 is a heating power supply, 11 is an ion extraction power supply, and 12 is Ion acceleration power source, 13 is a lens power source, 14 and 15 are beam deflection power sources, 16 and 17 are insulating terminals, and 18 is a vacuum gauge.
FIBによるイオン注入時に、エミッタ2の表面に付着し
た炭素は、以下に示す方法で除去される。鏡筒1を1×
10-6Torr程度の真空まで排気した後、バルブ8を開口
し、ガス導入管9を通して水素(H2)ガスを導入する。During the ion implantation by FIB, carbon attached to the surface of the emitter 2 is removed by the method described below. 1x lens barrel 1
After evacuating to a vacuum of about 10 −6 Torr, the valve 8 is opened and hydrogen (H 2 ) gas is introduced through the gas introducing pipe 9.
H2ガスは鏡筒1が1×10-3Torr程度の真空になるまで導
入する。その後、エミッタ2と、引き出し電極4との間
にイオン引き出し電源11を用いて、5〜10kVの電流
電圧を加える。この状態で、エミッタ2と引き出し電極
4との間に放電が起こり、通常1〜10mA程度のイオン
電流が流れる。これにより、エミッタ2の表面に付着し
た炭素は炭化水素(CmHn(m,n=整数))化し、エミ
ッタ2の表面から揮発し、それ故清浄化される。この表
面処理は、通常、LMISの動作前ないしは動作後に行な
う。The H 2 gas is introduced until the lens barrel 1 becomes a vacuum of about 1 × 10 −3 Torr. After that, a current voltage of 5 to 10 kV is applied between the emitter 2 and the extraction electrode 4 by using the ion extraction power supply 11. In this state, a discharge occurs between the emitter 2 and the extraction electrode 4, and an ion current of about 1 to 10 mA usually flows. As a result, the carbon attached to the surface of the emitter 2 becomes a hydrocarbon (C m H n (m, n = integer)), volatilizes from the surface of the emitter 2, and is therefore cleaned. This surface treatment is usually performed before or after the operation of LMIS.
第2図はPd-Ni-As-B〔Pd:Ni:As:B=3:3:2:2〕の共晶合
金を用いたLMISの引き出し電圧(VEX)−イオン電流
(Ii)放出特性である。引き出し電圧VEXは、イオン引
き出し電流11により、操作し、イオン電流Iiは、試料
7の位置で測定した。第2図において(a)はイオン源動
作20時間経過後の放出特性であり、この状態では、エ
ミッタ2は炭素により汚染されている。第2図において
(b)は第2図(a)の状態で水素放電を10分間ほどこした
場合のイオン源の放出特性であり、(a)に比べ(b)の方が
引き出し電圧VEXに対するイオン電流Iiが大きく安定し
ていることがわかる。第3図はLMISのエミッタ2の先端
部分の組成分析(Augerスペクトル)した結果を示す。
第3図において(a)はイオン源動作20時間経過後、水
素放電を行なう前の組成、第3図において(b)はイオン
源動作20時間経過後、水素放電を10分間ほどこした
後の組成分析結果である。Figure 2 shows the extraction voltage (V EX ) -ion current (I i ) of LMIS using a eutectic alloy of Pd-Ni-As-B [Pd: Ni: As: B = 3: 3: 2: 2]. It is a release characteristic. The extraction voltage V EX was operated by the ion extraction current 11, and the ion current I i was measured at the position of the sample 7. In FIG. 2, (a) shows the emission characteristics after 20 hours of operation of the ion source, and in this state, the emitter 2 is contaminated with carbon. In Figure 2
(b) shows the emission characteristics of the ion source when hydrogen discharge is applied for about 10 minutes in the state of FIG. 2 (a). Compared to (a), (b) is the ion current I i with respect to the extraction voltage V EX. It can be seen that is large and stable. FIG. 3 shows the result of composition analysis (Auger spectrum) of the tip of the emitter 2 of LMIS.
In FIG. 3, (a) shows the composition after the ion source operation for 20 hours and before the hydrogen discharge, and (b) in FIG. 3 shows the composition after the ion source operation for 20 hours and the hydrogen discharge for about 10 minutes. It is an analysis result.
第3図に示されるように、水素放電後では、エミッタ表
面に付着した炭素が除去されていることがわかる。この
水素放電処理により、エミッタ2表面での液体金属の流
れを抑止する汚染が除去され、再び、清浄なLMISの表面
が露出する。As shown in FIG. 3, it is understood that the carbon adhering to the emitter surface is removed after the hydrogen discharge. By this hydrogen discharge treatment, the contamination that suppresses the flow of the liquid metal on the surface of the emitter 2 is removed, and the clean surface of the LMIS is exposed again.
第2図および第3図に示した結果は、上記に示した水素
放電以外に、Arガスをガス導入管9を通して導入し、且
つLMIS部分を放電させ物理スパッタにより、表面汚染を
除去する方法においても同様の効果が得られる。The results shown in FIG. 2 and FIG. 3 are obtained in the method of removing surface contamination by physical sputtering by introducing Ar gas through the gas introducing tube 9 and discharging the LMIS portion in addition to the hydrogen discharge described above. Also has the same effect.
(発明の効果) 以上詳細に説明したように本発明による水素放電を行な
うことにより、エミッタ表面の炭素が炭素原子含有化合
物(CmHn(m,n1,整数))となり、揮発するの
で、LMISが清浄され、イオン化すべき合金の流れが安定
し、良好なイオン放出特性を得ることができる。(Effect of the Invention) As described in detail above, by performing hydrogen discharge according to the present invention, carbon on the emitter surface becomes a carbon atom-containing compound (C m H n (m, n1, integer)) and volatilizes. The LMIS is cleaned, the flow of the alloy to be ionized is stable, and good ion emission characteristics can be obtained.
また、Arガスを用いた放電を行なうことにおいても、ス
パッタにより炭素が除去できるので上記と同一の効果を
得ることができる。Also, when performing discharge using Ar gas, carbon can be removed by sputtering, and the same effect as described above can be obtained.
第1図は、本発明の実施例を説明するための、FIB装置
の概略構成図、第2図はLMISの引き出し電圧−イオン電
流放出特性を示す図、第3図はLMISのエミッタ先端の組
成分析図である。FIG. 1 is a schematic configuration diagram of an FIB device for explaining an embodiment of the present invention, FIG. 2 is a diagram showing extraction voltage-ion current emission characteristics of LMIS, and FIG. 3 is a composition of an emitter tip of LMIS. It is an analysis chart.
Claims (1)
と、エミッタと、引き出し電極とを有する液体金属イオ
ン源の清浄化方法において、 水素ガスとアルゴンガスのいずれか一方または両方を前
記液体金属イオン源に供給した後、前記エミッタと前記
引き出し電極との間に電圧を加えて放電を起こし、 この放電により、前記エミッタ表面に付着した炭素を炭
化水素化して揮発させるか、前記エミッタに付着した炭
素をスパッタして除去することを特徴とする液体金属イ
オン源の清浄化方法。1. A method for cleaning a liquid metal ion source having a reservoir for melting and holding a metal to be ionized, an emitter, and an extraction electrode, wherein one or both of hydrogen gas and argon gas are used for the liquid metal. After supplying to the ion source, a voltage is applied between the emitter and the extraction electrode to cause discharge, and the discharge causes carbon adhering to the surface of the emitter to be converted into hydrocarbon and volatilized, or adhered to the emitter. A method for cleaning a liquid metal ion source, which comprises removing carbon by sputtering.
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62204254A JPH0618109B2 (en) | 1987-08-19 | 1987-08-19 | Liquid metal ion source cleaning method |
| US07/227,255 US4892752A (en) | 1987-08-12 | 1988-08-02 | Method of ion implantation |
| DE3855897T DE3855897T2 (en) | 1987-08-12 | 1988-08-11 | Ion implantation method |
| EP88307442A EP0303486B1 (en) | 1987-08-12 | 1988-08-11 | Method of ion implantation |
| KR1019880010320A KR920005348B1 (en) | 1987-08-12 | 1988-08-12 | Ion implantation method |
| US07/371,976 US4946706A (en) | 1987-08-12 | 1989-06-27 | Method of ion implantation |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62204254A JPH0618109B2 (en) | 1987-08-19 | 1987-08-19 | Liquid metal ion source cleaning method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6448353A JPS6448353A (en) | 1989-02-22 |
| JPH0618109B2 true JPH0618109B2 (en) | 1994-03-09 |
Family
ID=16487415
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62204254A Expired - Lifetime JPH0618109B2 (en) | 1987-08-12 | 1987-08-19 | Liquid metal ion source cleaning method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0618109B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009187950A (en) * | 2008-02-08 | 2009-08-20 | Ict Integrated Circuit Testing Ges Fuer Halbleiterprueftechnik Mbh | Dual-mode gas field ion source |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6056342A (en) * | 1983-09-08 | 1985-04-01 | Anelva Corp | Ion beam generating apparatus |
| JPS6122537A (en) * | 1984-07-09 | 1986-01-31 | Hitachi Ltd | liquid metal ion source |
-
1987
- 1987-08-19 JP JP62204254A patent/JPH0618109B2/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009187950A (en) * | 2008-02-08 | 2009-08-20 | Ict Integrated Circuit Testing Ges Fuer Halbleiterprueftechnik Mbh | Dual-mode gas field ion source |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6448353A (en) | 1989-02-22 |
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