JPH01196816A - Introduction of impurity - Google Patents
Introduction of impurityInfo
- Publication number
- JPH01196816A JPH01196816A JP63023090A JP2309088A JPH01196816A JP H01196816 A JPH01196816 A JP H01196816A JP 63023090 A JP63023090 A JP 63023090A JP 2309088 A JP2309088 A JP 2309088A JP H01196816 A JPH01196816 A JP H01196816A
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- JP
- Japan
- Prior art keywords
- doping
- atmosphere
- gas
- tube
- impurity
- Prior art date
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Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、半導体装置の製造方法であって特に、基板に
熱処理により、不純物を導入する方法に関する。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a method of manufacturing a semiconductor device, and more particularly to a method of introducing impurities into a substrate by heat treatment.
従来の技術
従来より行なわれているSiウェーノーへのドーピング
層形成の1方法として、固相拡散法がある。2. Description of the Related Art One conventional method for forming a doped layer on Si wafer is the solid phase diffusion method.
この方法は、ウェーノ・と同形状の固体拡散源、及び、
81 ウェーハを石英チューブ内に入れて、不活性ガス
雰囲気中で、常圧下に於て8oo℃〜10oQ℃の高温
にする事により、不純物原子を拡散源からウェーハ表面
に移動させて、不純物をSi 中に拡散させるものであ
る。(R、K 、Tressler等0.ソリッド ス
テート テクノロジー(S01工dstate tec
hnology ) 日本版、p54−60.12日
(1984年)、〕
発明が解決しようとする課題
従来の方法では、少なくともSOO℃〜900℃程度の
高温を要する為、サブミクロンの構造制御を必要とする
微細化デバイスの作成に用いると、前工程で導入した不
純物が再拡散するという問題点があった。この理由を、
例えば、ムS固体拡散源(ム$As04)の場合につい
て考える。AlAsO4は次式■の様な分解反応を起す
。This method uses a solid diffusion source with the same shape as Waeno, and
81 By placing the wafer in a quartz tube and heating it to a high temperature of 80°C to 100°C under normal pressure in an inert gas atmosphere, impurity atoms are transferred from the diffusion source to the wafer surface, and the impurities are converted to Si. It is meant to diffuse inside. (R, K, Tressler, etc.0.Solid state technology (S01 Engineering dstate tec
hnology) Japanese Edition, p54-60.12 (1984)] Problems to be Solved by the Invention Conventional methods require high temperatures of at least SOO°C to 900°C, so submicron structural control is required. When used to create miniaturized devices, there is a problem in that impurities introduced in the previous process re-diffuse. The reason for this is
For example, consider the case of a MuS solid diffusion source (Mu$As04). AlAsO4 undergoes a decomposition reaction as shown in the following formula (2).
2U!AS04(solid):ム’J203(sol
id)十人s203(gas)+02 (gas )
−−−(ト)
AlAsO4は熱分解を起し、生成されたAs2O3が
81表面へ飛来し、砒素原子と酸素原子に分解し人Sは
Si中に拡散してドーピング層を形成する。従って熱分
解温度より高温にしないとドーピングはできない。その
為、ム5203の場合、860°C以上の温度を要した
。2U! AS04 (solid): Mu'J203 (sol
id) Ten people s203 (gas) +02 (gas)
---(g) AlAsO4 undergoes thermal decomposition, and the generated As2O3 flies to the surface of 81 and decomposes into arsenic atoms and oxygen atoms, and S diffuses into Si to form a doped layer. Therefore, doping cannot be performed unless the temperature is higher than the thermal decomposition temperature. Therefore, in the case of Mu5203, a temperature of 860°C or higher was required.
課題を解決するための手段
そこで、本発明においては、たとえばム1ist4゜5
iP20.又はBN等を含む平板を81基板とほぼ平行
に配置し、不活性ガス又はこれに微量の酸素を含むガス
雰囲気中で、減圧下においてプラズマを発生させながら
低温で熱処理を施す工程を含む方法を採用する。Means for Solving the Problems Therefore, in the present invention, for example,
iP20. Alternatively, a method including a step of arranging a flat plate containing BN or the like almost parallel to the 81 substrate and performing heat treatment at a low temperature while generating plasma under reduced pressure in an inert gas or a gas atmosphere containing a trace amount of oxygen. adopt.
作用
本発明では、上記拡散源の分解をプラズマにより促進す
る為、はぼ室温でもドーピングが可能である。Function: In the present invention, since the decomposition of the above-mentioned diffusion source is promoted by plasma, doping can be performed even at almost room temperature.
また、本発明は、減圧雰囲気下で行なわれる為。Furthermore, the present invention is carried out under a reduced pressure atmosphere.
不純物を含む分子の平均自由工程が大きくなり、例えば
、81基板表面に設けられたトレンチ溝の中へも不純物
を含む分子が侵入し易く、溝側壁へも均一なドーピング
層を形成する。The mean free path of the impurity-containing molecules becomes large, and for example, the impurity-containing molecules easily penetrate into the trenches provided on the surface of the 81 substrate, forming a uniform doping layer on the sidewalls of the trenches as well.
捷た減圧雰囲気にする事により、As、Pの相対濃度を
低くできるので1018−台の比較的低濃度領域に於て
も人s、Pの濃度の制御性も向上する。By creating a decompressed atmosphere, the relative concentrations of As and P can be lowered, so that the controllability of the concentrations of As and P can be improved even in a relatively low concentration region of 1018-level.
実施例
図は本発明の1実施例として、減圧プラズマ雰囲気の基
板熱処理装置の断面図を示す。石英チューブ6内に、ム
1kso4を表面に含んだウェーハと同形状のムS固体
拡散源6(例えば、カーボランダム社製、ムs 1oo
oL )とSlつx −” 7 f、1枚の固体拡散源
の両側に、1枚づつ配置した石英ボート8を挿入する。Embodiment The figure shows a sectional view of a substrate heat treatment apparatus in a reduced pressure plasma atmosphere as an embodiment of the present invention. In the quartz tube 6, a MU S solid diffusion source 6 having the same shape as the wafer containing MU 1KSO4 on the surface (for example, MU S 1OO made by Carborundum) is placed.
oL) and Slx-''7f, one quartz boat 8 is inserted on each side of one solid diffusion source.
雰囲気ガスとしては純度6Nのフルボ7 (Ar )と
50001)9m酸素(02)を含む、アルゴン/酸素
の混合体を使用する。アルゴンの流量1eooCC/分
、アルゴン/酸素の混合気体の流量’r100cc/分
に設定して、酸素の含有量を約700ppmとする。An argon/oxygen mixture containing fulvic 7 (Ar) with a purity of 6N and 50001)9m oxygen (02) is used as the atmospheric gas. The flow rate of argon is set to 1 eoo CC/min, and the flow rate of argon/oxygen mixed gas is set to 100 cc/min, so that the oxygen content is approximately 700 ppm.
チューブ内は、メカニカルポンプにより0.2Torr
の減圧雰囲気9に設定し、チューブ内温度は、外部ヒー
タ1oにより40Q℃に設定する。The inside of the tube is 0.2 Torr by a mechanical pump.
The reduced pressure atmosphere 9 is set to 9, and the temperature inside the tube is set to 40Q°C using an external heater 1o.
これは、プラズマにより温度は上昇するが、これでは温
度が不均一になるので、外部ヒータ1oにより温度を制
御し、均一性を向上させる為である。This is because although the temperature increases due to plasma, this makes the temperature non-uniform, so the temperature is controlled by the external heater 1o to improve uniformity.
この状態で、石英管内部のプラズマ電極12.13に高
周波電力と、直流バイ′アス電圧を印加する。In this state, high frequency power and DC bias voltage are applied to the plasma electrodes 12 and 13 inside the quartz tube.
この場合、高周波としては13.56 Ml−1,、直
流バイアス電圧は数百ボルト印加した。In this case, a high frequency of 13.56 Ml-1 and a DC bias voltage of several hundred volts were applied.
この時、分子の平均自由工程は、5μm程度になる事か
ら、6μm以下の深さのトレンチ溝には。At this time, the mean free path of molecules is about 5 μm, so for trenches with a depth of 6 μm or less.
底面でも不純物原子の到達量は表面と変わりなく溝側壁
2にも深さに関係なく均一にドーピング層3を形成でき
る。なお、プラズマを用いない場合。The amount of impurity atoms that reach the bottom surface is the same as that on the surface, and the doped layer 3 can be uniformly formed on the trench sidewall 2 regardless of the depth. In addition, when plasma is not used.
6インチ径の人S固体拡散源6より、熱分解して出テぐ
ル人5203の量は、900℃、酸素700ppm を
含んだアルゴン雰囲気では、30分間の熱処理により、
4.5 X 10”ケ発生する、減圧プラズマ雰囲気9
においては、それ以上のムSを発生させることが可能で
この量は、6インチウェーハの、4MDRAM相当のト
レンチ溝側壁にドーピングされるムSの必要量が約10
15ケ/ウヱーハである事から、発生量との間に約3桁
の差を有してお9、Asの基板への付着係数、及び、A
s 0として排気される量を考慮しても、十分な量であ
る。The amount of pyrolyzed 5203 released from the 6-inch diameter 6-inch solid diffusion source 6 was as follows:
4.5 x 10” generated reduced pressure plasma atmosphere 9
In this case, it is possible to generate more S than that amount, and the required amount of S to be doped on the sidewall of a trench corresponding to 4M DRAM in a 6-inch wafer is about 10.
Since it is 15 pieces/wafer, there is a difference of about 3 orders of magnitude between the generation amount and the adhesion coefficient of As to the substrate.
Even considering the amount exhausted as s0, this is a sufficient amount.
また、装置として、石英管の周囲に、高周波コイル全巻
いた物も使用できる。この場合、管内のプラズマの均一
性が向上し、外部から加熱する必要がない。Furthermore, a device in which a high-frequency coil is completely wound around a quartz tube can also be used. In this case, the uniformity of the plasma inside the tube is improved and there is no need for external heating.
発明の効果
以上の2うに、本発明を用いると、はぼ室温でも人Sや
P等をドーピングすることができる。これは、熱拡散で
はなく、プラズマ中に81等の基板を曝すことにより、
基板中に不純物が拡散されるものである。従って、前工
程で形成された不純物導入領域内の不純物が熱拡散によ
り再分布することは極めて少なくすることができる。Effects of the Invention As described above, by using the present invention, it is possible to dope S, P, etc. even at room temperature. This is not done by thermal diffusion, but by exposing the substrate such as 81 to plasma.
Impurities are diffused into the substrate. Therefore, redistribution of impurities in the impurity introduction region formed in the previous step due to thermal diffusion can be extremely reduced.
しかも、本発明の減圧プラズマ雰囲気下に於ける不純物
ドーピング方法を用いる事により、不純働程平均自由工
程が長くなりトレンチ溝側壁への均一ドーピングが可能
になった。又、開孔0.5μm、3μm深さのトレンチ
溝へのドーピング量の精密制御を、10 cm のオー
ダーで可能になった。又、低温、かつ減圧雰囲気で酸素
の巻き込みを押える事により、基板表面に酸化膜が形成
される事を防ぎ、制御性、均一性、再現性の良いドーピ
ングを可能にした。Moreover, by using the impurity doping method in a reduced pressure plasma atmosphere of the present invention, the mean free path of the impurity work becomes longer, making it possible to uniformly dope the side walls of the trench. Furthermore, it has become possible to precisely control the amount of doping into a trench with an opening of 0.5 μm and a depth of 3 μm on the order of 10 cm 2 . In addition, by suppressing the entrainment of oxygen at low temperatures and in a reduced pressure atmosphere, it is possible to prevent the formation of an oxide film on the substrate surface, making it possible to perform doping with good controllability, uniformity, and reproducibility.
図は本発明の方法を用いたドーピング装置の−構成例を
示す構成図である。
5・・・・・・石英チューブ、6・・・・・・人S固体
拡散源、7・・・・・・S1ウエーハ、8・・・・・・
石英ボート、9・・・・・・減圧雰囲気、1Q・・・・
・・外部ヒータ、12.13・・・・・・プラズマ発生
電極。
代理人の氏名 弁理士 中 尾 敏 男 ほか1名5−
ミー石英ナユ〜ブ
6−−−As固体=9.源
’7−−−SL ウェー7\
1O−−一タト部 ヒータ
/2,13−−−ブラスマ妾生電極The figure is a configuration diagram showing an example of the configuration of a doping apparatus using the method of the present invention. 5...Quartz tube, 6...S solid diffusion source, 7...S1 wafer, 8...
Quartz boat, 9... reduced pressure atmosphere, 1Q...
...External heater, 12.13...Plasma generation electrode. Name of agent: Patent attorney Toshio Nakao and 1 other person5-
Me quartz nayu ~bu 6---As solid = 9. Source '7---SL Way 7\ 1O---One part Heater/2,13---Brassma female electrode
Claims (2)
板をほぼ平行に配置し、不活性ガス、又はこれに微量の
酸素を含むガス雰囲気中で、減圧プラズマを発生させる
不純物導入方法。(1) An impurity introduction method in which a flat plate containing a doping impurity compound and a semiconductor substrate are arranged almost parallel to each other, and low-pressure plasma is generated in an atmosphere of an inert gas or a gas containing a trace amount of oxygen.
4、SiP_2O_7、又はBNを含む特許請求の範囲
第1項記載の不純物導入方法。(2) As a doping impurity compound, AlASO_
4. The impurity introduction method according to claim 1, which contains SiP_2O_7 or BN.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2309088A JPH0752723B2 (en) | 1988-02-02 | 1988-02-02 | Impurity introduction method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2309088A JPH0752723B2 (en) | 1988-02-02 | 1988-02-02 | Impurity introduction method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01196816A true JPH01196816A (en) | 1989-08-08 |
| JPH0752723B2 JPH0752723B2 (en) | 1995-06-05 |
Family
ID=12100729
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2309088A Expired - Lifetime JPH0752723B2 (en) | 1988-02-02 | 1988-02-02 | Impurity introduction method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0752723B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012104578A (en) * | 2010-11-09 | 2012-05-31 | Panasonic Corp | Plasma doping method and apparatus |
| CN102933897A (en) * | 2010-09-28 | 2013-02-13 | 李冰 | Lamp and method for generating diffuse reflection light |
-
1988
- 1988-02-02 JP JP2309088A patent/JPH0752723B2/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102933897A (en) * | 2010-09-28 | 2013-02-13 | 李冰 | Lamp and method for generating diffuse reflection light |
| JP2012104578A (en) * | 2010-11-09 | 2012-05-31 | Panasonic Corp | Plasma doping method and apparatus |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0752723B2 (en) | 1995-06-05 |
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