JPH04273142A - Ion implantation monitoring method - Google Patents
Ion implantation monitoring methodInfo
- Publication number
- JPH04273142A JPH04273142A JP3330591A JP3330591A JPH04273142A JP H04273142 A JPH04273142 A JP H04273142A JP 3330591 A JP3330591 A JP 3330591A JP 3330591 A JP3330591 A JP 3330591A JP H04273142 A JPH04273142 A JP H04273142A
- Authority
- JP
- Japan
- Prior art keywords
- dose
- oxide film
- board
- monitoring method
- substrate
- 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
Links
- 238000000034 method Methods 0.000 title claims abstract description 26
- 238000012544 monitoring process Methods 0.000 title claims abstract description 15
- 238000005468 ion implantation Methods 0.000 title claims description 8
- 238000002513 implantation Methods 0.000 claims abstract description 8
- 150000002500 ions Chemical class 0.000 claims abstract description 8
- 239000000758 substrate Substances 0.000 claims description 21
- 239000000523 sample Substances 0.000 abstract description 11
- 238000005259 measurement Methods 0.000 abstract description 7
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 239000007943 implant Substances 0.000 abstract 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 33
- 239000012535 impurity Substances 0.000 description 17
- 229910052681 coesite Inorganic materials 0.000 description 16
- 229910052906 cristobalite Inorganic materials 0.000 description 16
- 239000000377 silicon dioxide Substances 0.000 description 16
- 235000012239 silicon dioxide Nutrition 0.000 description 16
- 229910052682 stishovite Inorganic materials 0.000 description 16
- 229910052905 tridymite Inorganic materials 0.000 description 16
- 229910052710 silicon Inorganic materials 0.000 description 13
- 239000010703 silicon Substances 0.000 description 13
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 12
- 238000010586 diagram Methods 0.000 description 6
- 238000009826 distribution Methods 0.000 description 6
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- 238000000137 annealing Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 230000001066 destructive effect Effects 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 1
- -1 boron ion Chemical class 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 150000003376 silicon Chemical class 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
Abstract
Description
【0001】0001
【産業上の利用分野】本発明はイオン注入装置の管理方
法に関する。近年, イオン注入技法は半導体デバイス
製造プロセスに不可欠であるが, そのために速くて,
且つ正確なドーズモニタリング技術が必要になってき
ている。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for managing an ion implanter. In recent years, ion implantation techniques have become essential to semiconductor device manufacturing processes;
Moreover, accurate dose monitoring technology is becoming necessary.
【0002】0002
【従来の技術】従来のドーズモニタリング技術は, 高
ドーズ領域( ドーズ量が1x1014 cm −2以
上)に対してはイオン注入された測定試料(TP) の
シート抵抗を測定する方法によっているが, 低ドーズ
領域( ドーズ量が1x1014 cm −2 以下
)に対しては測定値が大きく, ドーズの変動に追従で
きないという難点があった。[Prior Art] Conventional dose monitoring technology relies on a method of measuring the sheet resistance of an ion-implanted measurement sample (TP) for high-dose regions (dose of 1x1014 cm-2 or more); The measurement value is large in the dose region (dose amount is 1 x 1014 cm -2 or less), and there is a problem in that it cannot follow changes in the dose.
【0003】近時, サーマプローブ法が登場してから
は低ドーズ領域に対しては約10分という短時間でTP
の結果が判明する状態になっている。 サーマプローブ
法はサーマプローブ(商品名 DTHERMA−PRO
BE 300, 製造元 THERMA−WAVE I
nc.) を使用してイオン注入された不純物に基づ
く結晶欠陥を光学的に測定し,これをドーズ量に換算す
る方法であるから, TPのアニーリングを行なう必要
はなく, 非破壊的測定方法であり且つ簡便である。[0003]Recently, since the appearance of the thermal probe method, TP can be completed in a short time of about 10 minutes for low dose regions.
The results are now known. The thermaprobe method is the thermaprobe (product name DTHERMA-PRO).
BE 300, Manufacturer THERMA-WAVE I
nc. ) is used to optically measure crystal defects based on ion-implanted impurities and convert this into a dose, so there is no need to TP annealing, and it is a non-destructive measurement method. It's simple.
【0004】一方, 高ドーズ領域に対して行なわれて
いる従来のシート抵抗の測定は, イオン注入されたT
Pをアニーリングし, その後, 酸化膜( シリコン
の場合はSiO2膜)を除去してから4端針測定器によ
って測定するために,結果が判明するまでに3乃至4
時間が必要である。
しかもこれは破壊的な方法であってTPを再利用するこ
とはできない。On the other hand, conventional sheet resistance measurements performed on high-dose regions are based on ion-implanted T
Because the P is annealed, the oxide film (SiO2 film in the case of silicon) is removed, and the measurement is performed using a four-point needle measuring device, it takes 3 to 4 hours before the results are known.
It takes time. Moreover, this is a destructive method and the TP cannot be reused.
【0005】[0005]
【発明が解決しようとする課題】そのために高ドーズ領
域に対しても, 当然 サーマプローブ法が適用される
べきである。然しサーマプローブ法において測定可能の
不純物濃度範囲は, ドーズ量が略1x1014 cm
−2 以下であって, サーマプローブ法を高ドー
ズ領域に対してモニタリングに利用することはできなか
った。[Problem to be Solved by the Invention] For this reason, the thermaprobe method should naturally be applied to high-dose regions as well. However, the impurity concentration range that can be measured using the thermaprobe method is approximately 1x1014 cm in dose.
-2 or less, making it impossible to use the thermaprobe method for monitoring high-dose regions.
【0006】そこで本発明の目的は, 高ドーズ領域に
対してもサーマプローブ法を適用してドーズモニタリン
グの効率が向上する方法を提供することであり, ひい
てはTPを再利用することによるコストダウンにも寄与
することである。[0006] Therefore, the purpose of the present invention is to provide a method that improves the efficiency of dose monitoring by applying the thermal probe method even to high dose regions, and further reduces costs by reusing TP. It is also a contribution.
【0007】[0007]
【課題を解決するための手段】上記の課題は, 注入基
板(TP)上に酸化膜を形成し, 該酸化膜を介して該
基板にイオン注入を行ない, サーマプローブ法を用い
てドーズ量を測定する方法及び,ドーズ量の測定後,
前記基板の酸化膜を除去し, 次いでこれを熱処理し,
改めて該基板上に酸化膜を形成し, 再度TPとして
利用する方法によって解決される。[Means for solving the problem] The above problem is solved by forming an oxide film on an implanted substrate (TP), implanting ions into the substrate through the oxide film, and controlling the dose using the therma probe method. How to measure and after measuring the dose,
Remove the oxide film on the substrate, then heat treat it,
The problem can be solved by forming an oxide film on the substrate again and using it as TP again.
【0008】図1 は本発明の原理説明図である。図中
, 実線はシリコン酸化膜(SiO2膜)が形成された
シリコン基板に高ドーズの不純物イオン注入を行なった
場合の不純物濃度分布を示している。又, 点線は S
iO2膜の無いシリコン基板に同様の条件で高ドーズの
不純物イオン注入を行なった場合の不純物濃度分布を示
している。SiO2膜のある場合にはシリコン基板に注
入される不純物は, SiO2膜の無い場合に較べると
一桁以上減少する。従って, この状態はサーマプロー
ブによる測定可能な範囲に入っているので, サーマプ
ローブによるモニタリングが実施できる。FIG. 1 is a diagram explaining the principle of the present invention. In the figure, the solid line indicates the impurity concentration distribution when a high dose of impurity ions is implanted into a silicon substrate on which a silicon oxide film (SiO2 film) is formed. Also, the dotted line is S
It shows the impurity concentration distribution when high-dose impurity ions are implanted into a silicon substrate without an iO2 film under similar conditions. When there is a SiO2 film, the amount of impurities implanted into the silicon substrate is reduced by more than an order of magnitude compared to when there is no SiO2 film. Therefore, since this condition is within the range that can be measured by the therm probe, monitoring using the therm probe can be carried out.
【0009】[0009]
【作用】SiO2膜中の不純物の拡散係数は, シリコ
ン基板中のそれよりも小さいことが知られている。従っ
て, SiO2膜は注入されたイオンをトラップするド
ーズトラップの性質を持つことになり, 大部分のイオ
ンはSiO2膜にトラップされてシリコン基板に注入さ
れる量は少なくなる。[Operation] It is known that the diffusion coefficient of impurities in a SiO2 film is smaller than that in a silicon substrate. Therefore, the SiO2 film has the property of a dose trap that traps the implanted ions, and most of the ions are trapped in the SiO2 film, reducing the amount implanted into the silicon substrate.
【0010】SiO2膜にトラップされる不純物の量は
, 注入エネルギーとSiO2膜の厚さに依存する。
従って, 常用の注入エネルギーで,シリコン基板中
に低ドーズ量が注入されるようにSiO2膜の厚さを設
定する。このようにSiO2膜の厚さを設定することに
ょって, 高ドーズ注入の場合も実際シリコン基板に注
入されるドーズ量は低ドーズになる。従って, この場
合サーマプローブ法による測定が可能になる。[0010] The amount of impurities trapped in the SiO2 film depends on the implantation energy and the thickness of the SiO2 film.
Therefore, the thickness of the SiO2 film is set so that a low dose is implanted into the silicon substrate using conventional implantation energy. By setting the thickness of the SiO2 film in this manner, even in the case of high-dose implantation, the actual dose implanted into the silicon substrate becomes low. Therefore, in this case, measurement using the thermaprobe method becomes possible.
【0011】図2 は, 注入エネルギーに対してSi
O2膜の厚さが不適当な場合の説明図である。 図2
(a)は, 高ドーズ量の不純物が全部シリコン基板中
に注入されている場合の不純物濃度分布を示している。
図2(b)は, 不純物濃度分布が図2(a)のよ
うな場合に, サーマプローブの出力(TW)が一定の
ドーズ量を越えると不安定になり,ドーズ量に比例しな
くなる様子を示している。[0011] Figure 2 shows the Si
FIG. 4 is an explanatory diagram of a case where the thickness of the O2 film is inappropriate. Figure 2
(a) shows the impurity concentration distribution when all high-dose impurities are implanted into the silicon substrate. Figure 2(b) shows how when the impurity concentration distribution is as shown in Figure 2(a), the output (TW) of the thermal probe becomes unstable and is no longer proportional to the dose when it exceeds a certain dose. It shows.
【0012】図3 は, 注入エネルギーに対してSi
O2膜の厚さが適当な場合の説明図である。図3(a)
は, 高ドーズ量の不純物の大部分がSiO2膜にトラ
ップされて, 少量の不純物がシリコンン基板中に注入
されている場合の不純物濃度分布を示している。図3(
b)は, 不純物濃度分布が図3(a)のような場合に
, サーマプローブの出力(TW)がドーズ量に比例し
ている様子を示している。この様な場合が, 高ドーズ
モニタリングが サーマプローブ法によって行なわれる
本発明の場合である。一般に, 不純物の拡散係数は基
板の酸化膜中の方が基板中よりも小さいので, 上記事
柄はシリコン以外の基板及びその酸化膜の組合わせに対
しても当てはまる。[0012] Figure 3 shows the Si
FIG. 4 is an explanatory diagram when the thickness of the O2 film is appropriate. Figure 3(a)
shows the impurity concentration distribution when most of the high-dose impurities are trapped in the SiO2 film and a small amount of impurities are implanted into the silicon substrate. Figure 3 (
Figure 3b) shows how the output (TW) of the thermal probe is proportional to the dose when the impurity concentration distribution is as shown in Figure 3(a). Such a case is the case of the present invention, in which high dose monitoring is performed by the thermaprobe method. Generally, the diffusion coefficient of impurities is smaller in the oxide film of the substrate than in the substrate, so the above also applies to combinations of substrates other than silicon and their oxide films.
【0013】[0013]
【実施例】本発明の実施例に対して説明する。p 型,
比抵抗が15Ωcmのシリコンウェファに対して通常
の表面洗浄を行って後に, このシリコンウェファ表面
に通常の熱酸化法により厚さ約100 nmのSiO2
膜を形成する。[Embodiment] An embodiment of the present invention will be explained. p type,
After performing normal surface cleaning on a silicon wafer with a specific resistance of 15 Ωcm, SiO2 with a thickness of approximately 100 nm is deposited on the surface of this silicon wafer using a normal thermal oxidation method.
Forms a film.
【0014】このウェファを高ドーズイオン注入のTP
として使用する。このTPに対して, 硼素イオン(B
+ ) をエネルギー15KeV, ドーズ量2x1
015 で注入を行う。その後,このTPをサーマプ
ローブ法によって測定する。 サーマプローブの出力
は注入のドース量に予めキャリイブレーションしてある
からサーマプローブの出力から直ちにドーズ量が得られ
る。 イオン注入を行って後, ドーズ量の値が得ら
れるまでの時間は20分乃至40分である。
このように, TPをサーマプローブ法によって測定す
ることにより高ドーズモニタリングを行なう。This wafer was subjected to high-dose ion implantation TP.
Use as. For this TP, boron ion (B
+) with an energy of 15KeV and a dose of 2x1
Injection is performed at 015. Thereafter, this TP is measured by the thermaprobe method. Since the output of the therma probe is calibrated in advance to the implantation dose, the dose can be obtained immediately from the output of the therma probe. After ion implantation, it takes 20 to 40 minutes to obtain a dose value. In this way, high dose monitoring is performed by measuring TP using the thermaprobe method.
【0015】このTPのSiO2膜を弗酸で除去し,
次いで, これを真空又は不活性ガス雰囲気中において
, 900 °C 乃至1000°で約30分間アニー
ルし, イオン注入に伴って生じた結晶欠陥を除去し,
改めて前記同様の酸化膜を形成すればこれを新しいT
Pとして再利用することができる。更に,またTPのS
iO2膜を除去せずに残し,不活性ガス雰囲気中におい
て同様のアニールを行い,これを新しいTPとして再利
用することもできる。[0015] This TP SiO2 film was removed with hydrofluoric acid,
This is then annealed at 900°C to 1000° for about 30 minutes in a vacuum or inert gas atmosphere to remove crystal defects caused by ion implantation.
If an oxide film similar to the above is formed again, this will become a new T.
It can be reused as P. Furthermore, TP's S
It is also possible to leave the iO2 film without removing it, perform similar annealing in an inert gas atmosphere, and reuse it as a new TP.
【0016】[0016]
【発明の効果】本発明によって, TPの測定結果が判
明するまでの時間が従来の1/5 に短縮されて, 高
ドーズイオン注入モニタリングの効率が格段に向上する
。又, TPは再利用することができる結果, コスト
ダウンにも寄与するところが大きい。[Effects of the Invention] According to the present invention, the time required to obtain TP measurement results is shortened to 1/5 of the conventional method, and the efficiency of high-dose ion implantation monitoring is greatly improved. Additionally, since TP can be reused, it greatly contributes to cost reduction.
【図1】 本発明の原理説明図である。FIG. 1 is a diagram explaining the principle of the present invention.
【図2】 注入エネルギーに対してSiO2膜の厚さ
が不適当な場合の説明図である。FIG. 2 is an explanatory diagram when the thickness of the SiO2 film is inappropriate for the implantation energy.
【図3】 注入エネルギーに対してSiO2膜の厚さ
が適当な場合の説明図である。FIG. 3 is an explanatory diagram when the thickness of the SiO2 film is appropriate for the implantation energy.
Claims (2)
ング方法において,注入基板上に酸化膜を形成する工程
と,該酸化膜を介して該基板にイオン注入を行なう工程
と, サーマプローブ法を用いてドーズ量を測定する工
程とを有することを特徴とするドーズモニタリング方法
。Claim 1. A dose monitoring method for high-dose ion implantation, which comprises: forming an oxide film on an implantation substrate; implanting ions into the substrate through the oxide film; and controlling the dose using a thermaprobe method. A dose monitoring method comprising the step of measuring the amount.
ング方法において,更に, ドーズ量の測定後, 前記
基板上に形成された酸化膜を除去する工程と,酸化膜が
除去された基板を熱処理する工程と, 再度, 該基板
上に酸化膜を形成する工程とを有することを特徴とする
請求項1記載のドーズモニタリング方法。2. A dose monitoring method for high-dose ion implantation, further comprising: after measuring the dose, removing an oxide film formed on the substrate; and heat-treating the substrate from which the oxide film has been removed. 2. The dose monitoring method according to claim 1, further comprising the steps of: forming an oxide film on the substrate again.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3033305A JP2626275B2 (en) | 1991-02-28 | 1991-02-28 | Ion implantation monitoring method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3033305A JP2626275B2 (en) | 1991-02-28 | 1991-02-28 | Ion implantation monitoring method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04273142A true JPH04273142A (en) | 1992-09-29 |
JP2626275B2 JP2626275B2 (en) | 1997-07-02 |
Family
ID=12382845
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3033305A Expired - Lifetime JP2626275B2 (en) | 1991-02-28 | 1991-02-28 | Ion implantation monitoring method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2626275B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105977181A (en) * | 2016-07-27 | 2016-09-28 | 上海华虹宏力半导体制造有限公司 | Method for monitoring quality of ion implantation equipment and ion implantation method |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62229934A (en) * | 1986-03-31 | 1987-10-08 | Toshiba Corp | Manufacture of semiconductor device |
JPH0246745A (en) * | 1988-07-01 | 1990-02-16 | Siemens Ag | Nondestructive detection of electronic nonuniformity |
JPH02283016A (en) * | 1989-04-25 | 1990-11-20 | Sony Corp | Forming method of semiconductor layer containing boron |
JPH0314251A (en) * | 1989-06-13 | 1991-01-22 | Toshiba Corp | Evaluation method for silicon semiconductor substrate |
-
1991
- 1991-02-28 JP JP3033305A patent/JP2626275B2/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62229934A (en) * | 1986-03-31 | 1987-10-08 | Toshiba Corp | Manufacture of semiconductor device |
JPH0246745A (en) * | 1988-07-01 | 1990-02-16 | Siemens Ag | Nondestructive detection of electronic nonuniformity |
JPH02283016A (en) * | 1989-04-25 | 1990-11-20 | Sony Corp | Forming method of semiconductor layer containing boron |
JPH0314251A (en) * | 1989-06-13 | 1991-01-22 | Toshiba Corp | Evaluation method for silicon semiconductor substrate |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105977181A (en) * | 2016-07-27 | 2016-09-28 | 上海华虹宏力半导体制造有限公司 | Method for monitoring quality of ion implantation equipment and ion implantation method |
Also Published As
Publication number | Publication date |
---|---|
JP2626275B2 (en) | 1997-07-02 |
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