JPH04138648A - Neutral particle mass analyzer - Google Patents

Neutral particle mass analyzer

Info

Publication number
JPH04138648A
JPH04138648A JP2261513A JP26151390A JPH04138648A JP H04138648 A JPH04138648 A JP H04138648A JP 2261513 A JP2261513 A JP 2261513A JP 26151390 A JP26151390 A JP 26151390A JP H04138648 A JPH04138648 A JP H04138648A
Authority
JP
Japan
Prior art keywords
ion
electrode
neutral particle
ions
generated
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
JP2261513A
Other languages
Japanese (ja)
Other versions
JP3055159B2 (en
Inventor
Yutaka Ido
豊 井戸
Yoshifumi Yoshioka
吉岡 善文
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.)
Shimadzu Corp
Original Assignee
Shimadzu 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 Shimadzu Corp filed Critical Shimadzu Corp
Priority to JP2261513A priority Critical patent/JP3055159B2/en
Publication of JPH04138648A publication Critical patent/JPH04138648A/en
Application granted granted Critical
Publication of JP3055159B2 publication Critical patent/JP3055159B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To improve mass resolution by constituting an ionizing chamber of a three-dimensional electrode, provided with an opening part for light to permeate and an opening part for an ion of ionizing a neutral particle to permeate, and a draw out electrode provided in parallel to the ion permeating opening part. CONSTITUTION:When a sample surface 3 is irradiated by a primary ion 2 from an ion gun 1, a neutral particle 5 or the like is generated. Next, the neutral particle 5 passes through an opening part 8 to advance into the inside of a cylindrical electrode 7. Then, laser light 14 is irradiated to light-ionize the neutral particle 5. Potential distribution is generated in the electrode 7 to decrease a spread of initial energy given to the ion, and an ion 15, generated in accordance with the potential distribution formed by the electrode 7 and a draw out electrode 16, is guided to a mass analyzing part 17. Thereafter, the ion 15 is converted into an electrical signal to analyze a sample element. In this way, mass resolution is improved, and deterioration of sensitivity by slight fluctuation of a converging point of laser light can be prevented by collecting the ion on the center axis.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は、分析する試料にイオンを照射し、試料表面よ
りスパッタされる中性粒子をポストイオン化して、その
イオンの質量分析を行う中性粒子質量分析装置、特に、
そのイオン化室に関する。
[Detailed Description of the Invention] [Industrial Application Field] The present invention is directed to a method in which a sample to be analyzed is irradiated with ions, neutral particles sputtered from the sample surface are post-ionized, and the ions are subjected to mass spectrometry. particle mass spectrometers, especially
Regarding the ionization chamber.

[従来技術] 現在、元素の微量分析方法として広く用いられている二
次イオン質量分析(SIMS)方法の欠点を補い、将来
SIMSを代替するものと期待されている中性粒子質量
分析(SNMS)方法が注目されている。試料面にイオ
ンビームを照射すると、試料面からは二次イオン、中性
粒子、電子等の粒子が放出され、これらの粒子を質量分
析することにより、試料の元素分析を行うことができる
[Prior art] Neutral particle mass spectrometry (SNMS) is expected to compensate for the shortcomings of secondary ion mass spectrometry (SIMS), which is currently widely used as a method for trace analysis of elements, and to replace SIMS in the future. The method is attracting attention. When the sample surface is irradiated with an ion beam, particles such as secondary ions, neutral particles, and electrons are emitted from the sample surface, and elemental analysis of the sample can be performed by mass spectrometry of these particles.

このとき発生する二次イオン量は試料種、試料表面の状
態によって敏感に変化し、測定が不安定で再現性に乏し
い。一方、試料面からの中性粒子の出易さは元素の特性
であり、共存他元素の影響も受けに<<、試料中のその
元素の濃度に比例して試料から放出される上、二次イオ
ンより放射量が大であるので、二次イオンの質量分析よ
りも中性粒子の質量分析のほうが有利と考えられている
The amount of secondary ions generated at this time changes sensitively depending on the sample type and the state of the sample surface, making measurement unstable and lacking in reproducibility. On the other hand, the ease with which neutral particles come out from the sample surface is a characteristic of the element, and is influenced by other coexisting elements. Mass spectrometry of neutral particles is considered more advantageous than mass spectrometry of secondary ions because the amount of radiation is larger than that of secondary ions.

従来の中性粒子質量分析装置を第4図により説明する。A conventional neutral particle mass spectrometer will be explained with reference to FIG.

第4図において、1はイオン銃、2は一次イオン、3は
被分析試料、4.5は発生した二次イオン及び中性粒子
、6はイオン化室であり、板電極61.62により均一
電界を発生している。13は集光用レンズ、14はレー
ザ光であり、光子エネルギーの高い紫外光で高い尖頭パ
ワーを持つエキシマレーザを用いることが多い。15は
多光子イオン化されたイオン、17は質量分析部、18
はイオン検出器、19はプリアンプ、20は測定及びデ
ータ処理装置である。なお、イオン銃1ないしイオン検
出器18はすべて高真空または超高真空の雰囲気中に置
かれている。
In Fig. 4, 1 is an ion gun, 2 is a primary ion, 3 is a sample to be analyzed, 4.5 is a generated secondary ion and neutral particles, 6 is an ionization chamber, and a uniform electric field is generated by plate electrodes 61 and 62. is occurring. Reference numeral 13 indicates a condensing lens, and reference numeral 14 indicates a laser beam, and an excimer laser having ultraviolet light with high photon energy and high peak power is often used. 15 is a multiphoton ionized ion, 17 is a mass spectrometer, 18
19 is an ion detector, 19 is a preamplifier, and 20 is a measurement and data processing device. Note that the ion gun 1 to the ion detector 18 are all placed in a high vacuum or ultrahigh vacuum atmosphere.

次に、この装置の動作を説明する。Next, the operation of this device will be explained.

イオン銃1からの一次イオン2によって試料表面3を照
射すると、試料表面3は照射された一次イオン2でスパ
ッタされ、二次イオン4や中性粒子5が発生する。発生
した二次イオン4は電極61に適当な電位を与えること
によって反射、除去される。中性粒子5はそのまま通過
し、電極61と電極62の間で、レンズ13で集光され
たレーザ光14が照射されることにより多光子イオン化
されるとともに、電極61と電極62の間の電界により
加速される。そして、多光子イオン化され、加速された
イオン15は質量分析部17を通り、イオン検出器18
で電気信号に変換された後、プリアンプ19を介して測
定及びデータ処理装置20に導かれ、試料元素が分析さ
れる。
When the sample surface 3 is irradiated with primary ions 2 from the ion gun 1, the sample surface 3 is sputtered with the irradiated primary ions 2, and secondary ions 4 and neutral particles 5 are generated. The generated secondary ions 4 are reflected and removed by applying an appropriate potential to the electrode 61. The neutral particles 5 pass through as they are, and are irradiated with the laser beam 14 focused by the lens 13 between the electrodes 61 and 62 to be multiphoton ionized, and the electric field between the electrodes 61 and 62 is is accelerated by Then, the multiphoton ionized and accelerated ions 15 pass through the mass spectrometer 17 and are detected by the ion detector 18.
After being converted into an electrical signal, the signal is guided to a measurement and data processing device 20 via a preamplifier 19, where the sample elements are analyzed.

[発明が解決しようとする課題] 従来の中性粒子質量分析装置は上記のように構成され、
板電極を平行に対峙させて均一電界を発生し、この空間
領域で高出力のパルスレーザを照射して多光子イオン化
することにより、ポストイオン化を行っており、イオン
化する領域がレーザ光をレンズで集光した集光径程度の
広がりを有している。従って、従来の中性粒子質量分析
装置のイオン化室の構造では第3図aのようにイオン化
領域の広がりに対応した加速イオンの初期エネルギー分
布が必然的に発生し、後に続く質量分析部での質量分解
能を低下させる一因となっている。
[Problem to be solved by the invention] A conventional neutral particle mass spectrometer is configured as described above,
Post-ionization is performed by arranging plate electrodes facing each other in parallel to generate a uniform electric field, and irradiating this spatial region with a high-power pulsed laser to produce multiphoton ionization. It has a spread approximately equal to the diameter of the condensed light. Therefore, in the structure of the ionization chamber of a conventional neutral particle mass spectrometer, an initial energy distribution of accelerated ions corresponding to the spread of the ionization region inevitably occurs as shown in Figure 3a, and the initial energy distribution of accelerated ions in the subsequent mass spectrometer This is one of the causes of lower mass resolution.

本発明は、上記のような従来技術の欠点を解消するため
に創案されたものであり、イオン化室での初期エネルギ
ーの広がりを抑え、質量分解能を向上することができる
中性粒子質量分析装置を提供することを目的とする。
The present invention was devised to eliminate the drawbacks of the prior art as described above, and provides a neutral particle mass spectrometer that can suppress the spread of initial energy in the ionization chamber and improve mass resolution. The purpose is to provide.

[課題を解決するための手段] 上記目的を達成するために、本発明の中性粒子質量分析
装置は、イオン化室を、光が通過する開孔部と、中性粒
子が通過する開孔部と、中性粒子をイオン化したイオン
が通過する開孔部とを設けた立体状電極と、上記イオン
通過開孔部に平行に設けられた引出し電極とで構成して
いる。
[Means for Solving the Problems] In order to achieve the above object, the neutral particle mass spectrometer of the present invention has an ionization chamber that has an aperture through which light passes and an aperture through which neutral particles pass. and an aperture through which ions obtained by ionizing neutral particles pass, and an extraction electrode provided in parallel to the ion-passing aperture.

[作用] 本発明の中性粒子質量分析装置は、上記のように構成さ
れており、立体状電極及び引出し電極に所定の電圧を引
加すると、立体状電極内部には従来のイオン化室のよう
に直線的な傾斜分布ではなく、イオン化領域の近傍では
ゆるやかな電位変化を有する電位分布が得られる。従っ
て、イオンに与えられる初期エネルギー分布も小さくな
り、質量分解能を改善することができる。
[Function] The neutral particle mass spectrometer of the present invention is configured as described above, and when a predetermined voltage is applied to the three-dimensional electrode and the extraction electrode, the interior of the three-dimensional electrode is similar to a conventional ionization chamber. Instead of a linearly sloped distribution, a potential distribution with gradual potential changes near the ionization region is obtained. Therefore, the initial energy distribution given to ions is also reduced, and mass resolution can be improved.

[実施例] 本発明の実施例を以下図面に基づいて説明する。[Example] Embodiments of the present invention will be described below based on the drawings.

第1図は本発明の実施例を示す図であり、1はイオン銃
、2は一次イオン、3は被分析試料、4.5は発生した
二次イオン及び中性粒子、6はシールド電極、7は円筒
状電極であり、開孔部8〜11を有している。12は絶
縁体、13は集光用レンズ、14は励起レーザ光1.1
5は多光子イオン化されたイオン、16は引出し電極、
17は質量分析部、18はイオン検出器、19はプリア
ンプ、20は測定及びデータ処理装置である。なお、イ
オン銃工ないしイオン検出器18はすべて高真空または
超高真空の雰囲気中に置かれている。
FIG. 1 is a diagram showing an embodiment of the present invention, in which 1 is an ion gun, 2 is a primary ion, 3 is a sample to be analyzed, 4.5 is a generated secondary ion and neutral particles, 6 is a shield electrode, 7 is a cylindrical electrode, which has openings 8-11. 12 is an insulator, 13 is a focusing lens, 14 is an excitation laser beam 1.1
5 is a multiphoton ionized ion, 16 is an extraction electrode,
17 is a mass spectrometer, 18 is an ion detector, 19 is a preamplifier, and 20 is a measurement and data processing device. Incidentally, the ion gun device or the ion detector 18 are all placed in a high vacuum or ultrahigh vacuum atmosphere.

円筒状電極7と引出し電極16間に所定の電圧を引加す
ると、円筒状電極の内部には、第2図に示すような非直
線的な電位分布が発生する。
When a predetermined voltage is applied between the cylindrical electrode 7 and the extraction electrode 16, a nonlinear potential distribution as shown in FIG. 2 is generated inside the cylindrical electrode.

この分析装置を用いた試料元素の分析動作を説明する。The operation of analyzing sample elements using this analyzer will be explained.

イオン銃1からの一次イオン2によって試料表面3を照
射すると、試料表面3は照射された一次イオン2でスパ
ッタされ、二次イオン4や中性粒子5が発生する。発生
した二次イオン4はシールド電極6と円筒状電極7とが
作る反射電界により反射、除去される。一方、発生した
中性粒子5は開孔部8を通って円筒状電極内部に入り、
レンズ13で集2光されたレーザ光14が開孔部9を通
って照射されることにより光イオン化される。使用済み
のレーザ光は開孔部10通って円筒状電極7の外へ出る
。このとき、上記のように円筒状電極7の内部には、第
2図に示すような非直線的変化を有する電位分布が発生
しているので、第3図すに示すようにイオンに与えられ
る初期エネルギーの広がりは非常に小さくなる。発生し
たイオン15は円筒状電極7と引出し電極16によって
形成される電位分布にしたがって開孔部11を通って質
量分析部17へ導かれる。質量分析部17を通過したイ
オンはイオン検出器18で電気信号に変換された後、プ
リアンプ19を介して測定及びデータ処理装置20に導
かれ、試料元素が分析される。
When the sample surface 3 is irradiated with primary ions 2 from the ion gun 1, the sample surface 3 is sputtered with the irradiated primary ions 2, and secondary ions 4 and neutral particles 5 are generated. The generated secondary ions 4 are reflected and removed by the reflected electric field created by the shield electrode 6 and the cylindrical electrode 7. On the other hand, the generated neutral particles 5 enter the inside of the cylindrical electrode through the opening 8.
The laser beam 14 focused by the lens 13 is irradiated through the aperture 9 and photoionized. The used laser light exits the cylindrical electrode 7 through the aperture 10. At this time, as described above, a potential distribution with a nonlinear change as shown in FIG. 2 is generated inside the cylindrical electrode 7, so that the potential distribution is applied to the ions as shown in FIG. 3. The initial energy spread becomes very small. The generated ions 15 are guided to the mass spectrometer 17 through the aperture 11 according to the potential distribution formed by the cylindrical electrode 7 and the extraction electrode 16. The ions that have passed through the mass spectrometer 17 are converted into electrical signals by the ion detector 18, and then guided to the measurement and data processing device 20 via the preamplifier 19, where the sample elements are analyzed.

なお、上記実施例では円筒状電極を使用したが、この電
極を立方体又は直方体形状としても、同様な効果を得る
ことができる。
Although a cylindrical electrode was used in the above embodiment, the same effect can be obtained by using a cubic or rectangular parallelepiped electrode.

[発明の効果] 本発明は、以上のように、イオン化室を立体状電極と引
出し電極とで構成しているので、立体状電極内部には従
来のイオン化室のように直線的な傾斜分布ではなく、イ
オン化領域の近傍ではゆるやかな電位変化を有する電位
分布が得られる。従って、イオンに与えられる初期エネ
ルギー分布が小さくなり、質量分解能を改善することが
できる。
[Effects of the Invention] As described above, in the present invention, since the ionization chamber is constituted by a three-dimensional electrode and an extraction electrode, there is no linear gradient distribution inside the three-dimensional electrode unlike in the conventional ionization chamber. Therefore, a potential distribution with gradual potential changes is obtained in the vicinity of the ionization region. Therefore, the initial energy distribution given to the ions becomes smaller, and mass resolution can be improved.

また、電位分布の形状がイオンを中心軸上に集める効果
があり、レーザ光の集光点が多少変動し、イオン発生点
が中心軸上になくとも感度の低下を防止することができ
る。
In addition, the shape of the potential distribution has the effect of concentrating ions on the central axis, and even if the focal point of the laser beam changes somewhat and the ion generation point is not on the central axis, it is possible to prevent a decrease in sensitivity.

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

第1図は本発明の中性粒子質量分析装置を示す図、第2
図は円筒状電極内部での電位分布を示す図、第3図は円
筒状電極内部での電位分布とイオン初期エネルギーの広
がりの関係を示す図、第4図は従来の中性粒子質量分析
装置を示す図である。 1・・・・・・イオン銃、2・・・・・・−次イオン、
3・・・・・・被分析試料、4・・・・・・二次イオン
、5・・・・・・中性粒子、6・・・・・・シールド電
極、7・・・・・・円筒状電極、8〜11・・・・・・
開孔部、12・・・・・・絶縁体、13・・・・・・集
光用レンズ、14・・・・・・励起レーザ光、15・・
・・・・中性粒子がイオン化されたイオン、16・・・
・・・引出し電極、17・・・・・・質量分析部、18
・・・・・・イオン検出器、19・・・・・・プリアン
プ、20・・・・・・測定及びデータ処理装置
Figure 1 is a diagram showing the neutral particle mass spectrometer of the present invention, Figure 2 is a diagram showing the neutral particle mass spectrometer of the present invention.
The figure shows the potential distribution inside the cylindrical electrode. Figure 3 shows the relationship between the potential distribution inside the cylindrical electrode and the spread of ion initial energy. Figure 4 shows the conventional neutral particle mass spectrometer. FIG. 1...Ion gun, 2...-Next ion,
3... Sample to be analyzed, 4... Secondary ions, 5... Neutral particles, 6... Shield electrode, 7... Cylindrical electrode, 8-11...
Opening portion, 12... Insulator, 13... Focusing lens, 14... Excitation laser beam, 15...
...Ions that are ionized neutral particles, 16...
... Extraction electrode, 17 ... Mass spectrometry section, 18
...Ion detector, 19 ...Preamplifier, 20 ...Measurement and data processing device

Claims (1)

【特許請求の範囲】[Claims] (1)分析する試料にイオンを照射し、試料表面よりス
パッタされる中性粒子をポストイオン化して、そのイオ
ンの質量分析を行う中性粒子質量分析装置において、光
が通過する開孔部と、中性粒子が通過する開孔部と、中
性粒子をイオン化したイオンが通過する開孔部とを設け
た立体状電極と、上記イオン通過開孔部に平行に設けら
れた引出し電極とでイオン化室を構成したことを特徴と
する中性粒子質量分析装置。
(1) In a neutral particle mass spectrometer that irradiates the sample to be analyzed with ions, post-ionizes the neutral particles sputtered from the sample surface, and performs mass spectrometry on the ions, there is an opening through which light passes. , a three-dimensional electrode provided with an aperture through which neutral particles pass, an aperture through which ions obtained by ionizing the neutral particles pass, and an extraction electrode provided in parallel to the ion-passing aperture. A neutral particle mass spectrometer comprising an ionization chamber.
JP2261513A 1990-09-28 1990-09-28 Neutral particle mass spectrometer Expired - Fee Related JP3055159B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2261513A JP3055159B2 (en) 1990-09-28 1990-09-28 Neutral particle mass spectrometer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2261513A JP3055159B2 (en) 1990-09-28 1990-09-28 Neutral particle mass spectrometer

Publications (2)

Publication Number Publication Date
JPH04138648A true JPH04138648A (en) 1992-05-13
JP3055159B2 JP3055159B2 (en) 2000-06-26

Family

ID=17362950

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2261513A Expired - Fee Related JP3055159B2 (en) 1990-09-28 1990-09-28 Neutral particle mass spectrometer

Country Status (1)

Country Link
JP (1) JP3055159B2 (en)

Also Published As

Publication number Publication date
JP3055159B2 (en) 2000-06-26

Similar Documents

Publication Publication Date Title
US4442354A (en) Sputter initiated resonance ionization spectrometry
US4686366A (en) Laser mass spectrometer
US9035244B2 (en) Automatic gain control with defocusing lens
US5365063A (en) Method and apparatus of quantitative non-resonant photoionization of neutral particles and the use of such apparatus
Ebata et al. Development of laser ionization mass nanoscope (LIMAS)
JPS5829578B2 (en) Sonoi ion Senbetsu Sochi
Held et al. Molecular Cesium Component in Multiphoton Ionization of a Cesium Atomic Beam by a Q-Switched Neodymium-Glass Laser at 1.06 μm
US5204530A (en) Noise reduction in negative-ion quadrupole mass spectrometry
US5763875A (en) Method and apparatus for quantitative, non-resonant photoionization of neutral particles
JP3055159B2 (en) Neutral particle mass spectrometer
WO2018092271A1 (en) Ion analyzer
JP3055160B2 (en) Neutral particle mass spectrometer
Miltenberger Secondary ion emission in MeV-SIMS
JP6309381B2 (en) Mass spectrometer and mass spectrometry method
JP3079585B2 (en) Neutral particle mass spectrometer
JPH06103625B2 (en) Ion micro analyzer
JPH04233149A (en) Analyzing device for surface of sample
JP2707097B2 (en) Method and apparatus for ionizing sputtered neutral particles
JPH0622109B2 (en) Secondary ion mass spectrometer
JP3140557B2 (en) Laser ionization neutral particle mass spectrometer and analysis method using the same
KR20000033909A (en) Mass spectrometer and spectrometry
JPH05251035A (en) Spatter neutral particle mass spectrometry device
JPS59201357A (en) Secondary ion mass spectrometer
JPH0828202B2 (en) Secondary Neutral Particle Mass Spectrometer
Rottmann et al. Technical background

Legal Events

Date Code Title Description
FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20080414

Year of fee payment: 8

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090414

Year of fee payment: 9

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100414

Year of fee payment: 10

LAPS Cancellation because of no payment of annual fees