JPH01196116A - Manufacture of polycrystalline silicon thin film - Google Patents
Manufacture of polycrystalline silicon thin filmInfo
- Publication number
- JPH01196116A JPH01196116A JP1967488A JP1967488A JPH01196116A JP H01196116 A JPH01196116 A JP H01196116A JP 1967488 A JP1967488 A JP 1967488A JP 1967488 A JP1967488 A JP 1967488A JP H01196116 A JPH01196116 A JP H01196116A
- Authority
- JP
- Japan
- Prior art keywords
- substrate
- thin film
- silicon thin
- amorphous silicon
- polycrystalline silicon
- 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
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- Recrystallisation Techniques (AREA)
Abstract
Description
【発明の詳細な説明】
[技術分野]
本発明は多結晶シリコン薄膜の製法に関し、特に低温に
おける多結晶シリコン薄;1りの形成に関する。DETAILED DESCRIPTION OF THE INVENTION [Technical Field] The present invention relates to a method for manufacturing polycrystalline silicon thin films, and particularly to the formation of polycrystalline silicon thin films at low temperatures.
[背景技術]
薄膜半導体装置として結晶質や非晶質の半導体薄膜が利
用されている。結晶質の半導体薄膜として、単結晶薄膜
や多結晶の薄膜が多数使用されている。多結晶薄膜は各
種の基板上に形成されて用いられるが、結晶化促進のた
めに、多結晶薄膜の形成時に基板温度を高温化せねばな
らないと云う問題点があり、または低温で形成された後
、高温におけるアニール工程を必要としていた。このた
めに、基板としては高温に耐える材料が要求されていた
。高温耐性の基板はコストア・ンプとなり、また基板の
種類も限られたものとなっていた。[Background Art] Crystalline and amorphous semiconductor thin films are used as thin film semiconductor devices. Many single crystal thin films and polycrystalline thin films are used as crystalline semiconductor thin films. Polycrystalline thin films are used by being formed on various substrates, but there is a problem in that the substrate temperature must be raised to a high temperature when forming the polycrystalline thin film to promote crystallization, or After that, a high-temperature annealing process was required. For this reason, materials that can withstand high temperatures have been required for the substrate. High-temperature resistant substrates are costly, and the types of substrates available are also limited.
しかして、安価で実用性のあるガラス基板のなかでも、
青板ガラスはもっともコストが低く、かつ、大量に生産
されているものであるが、高温における耐久性に乏しい
ため、多結晶薄膜形成用の基板としてはいままで、用い
ることができなかった。However, among the inexpensive and practical glass substrates,
Although blue plate glass has the lowest cost and is produced in large quantities, it has until now been unable to be used as a substrate for forming polycrystalline thin films because of its poor durability at high temperatures.
本発明者らは、かかる点に鑑の鋭意検討した結果、青板
ガラスの使用をも可能にする効果的な低温での結晶成長
の促進方法を見いだしたので、ここにその技術内容を詳
細に開示するとともに、代償として独占排他権たる特許
権の付与を請求するものである。As a result of intensive investigation into this point, the present inventors have discovered an effective method for promoting crystal growth at low temperatures that also enables the use of soda-lime glass.The present inventors hereby disclose the technical content in detail. At the same time, it requests the granting of patent rights, which are exclusive and exclusive rights, in return.
[発明の開示]
本発明は、基板を加熱しつつ、基板上に形成された非晶
質シリコン薄膜に光を照射することを特徴とするもので
ある。[Disclosure of the Invention] The present invention is characterized in that an amorphous silicon thin film formed on a substrate is irradiated with light while heating the substrate.
本発明において用いられる光は、レーザー光線のような
スペクトル幅の狭い光でもスペクトル幅の広い光でもよ
い。好ましくは、非晶質シリコンの吸収係数の大きい1
μm以下の波長を有する光である。とくに、好ましくは
照射光の光子数を大きく出来る可視光ならびに紫外線レ
ーザーが用いられる。具体的には、アルゴンイオンレー
ザ−やNd¥ACレーザーなどが好ましい。The light used in the present invention may be light with a narrow spectrum width such as a laser beam or light with a wide spectrum width. Preferably, 1 has a large absorption coefficient of amorphous silicon.
It is light having a wavelength of μm or less. In particular, visible light and ultraviolet lasers, which can increase the number of photons of irradiated light, are preferably used. Specifically, argon ion laser, Nd\AC laser, etc. are preferable.
本発明において、基板の加熱温度は600 ’C以下で
十分である。好ましくは、400〜600°C程度の温
度に加熱される。この温度領域においては、青板ガラス
も十分に使用可能である。該基板の加熱は遠赤外綿ヒー
タ、シースヒータやランプヒータ等を単独または併用し
て行われる。ランプヒータは可視光のスペクトルを含む
ので非晶質シリコンの吸収係数が大きく基板ならびに非
晶質シリコン薄膜の温度上昇に効果的であり、用いるに
好ましい。In the present invention, it is sufficient to heat the substrate at a temperature of 600'C or less. Preferably, it is heated to a temperature of about 400 to 600°C. In this temperature range, blue plate glass can also be used satisfactorily. The substrate is heated using a far-infrared cotton heater, a sheath heater, a lamp heater, etc. alone or in combination. Since the lamp heater includes the visible light spectrum, the absorption coefficient of amorphous silicon is large, and it is effective in raising the temperature of the substrate and the amorphous silicon thin film, and is therefore preferably used.
本発明に用いることのできる非晶質シリコン薄膜はプラ
ズマCVD法、マイクロ波CVD法、スパッター法や熱
CVD法等で形成されるものであり、−船釣に水素化非
晶質シリコンとしてよびなられされているものが用いら
れる。非晶質シリコンは不純物を含有していてもよいし
、意図的に不純物を導入しないものでもよい。不純物と
して、■族や■族の不純物を含有する非晶質シリコン薄
膜を用いることにより得られる多結晶薄膜はそれぞれ、
P型およびN型の電気伝導性を示す。意図的に不純物が
導入されていない非晶質シリコンは弱P型または弱N型
の電気伝導性を示す多結晶薄膜を与える。非晶質シリコ
ンゲルマン合金や非晶質ソリコンカーボン合金も本発明
の原料とすることができる。The amorphous silicon thin film that can be used in the present invention is formed by a plasma CVD method, a microwave CVD method, a sputtering method, a thermal CVD method, etc. What is specified is used. The amorphous silicon may contain impurities, or may not contain any impurities intentionally. Polycrystalline thin films obtained by using an amorphous silicon thin film containing group ■ or group ■ impurities as impurities are as follows:
Shows P-type and N-type electrical conductivity. Amorphous silicon to which impurities are not intentionally introduced provides a polycrystalline thin film exhibiting weak P-type or weak N-type electrical conductivity. Amorphous silicon-germane alloys and amorphous solicon carbon alloys can also be used as raw materials for the present invention.
本発明の別の特徴は低温における多結晶薄膜の成長速度
を効果的に増大できることである。本発明で用いる温度
領域においては、通常、5人/秒以上のような高速度で
シリコン薄膜を堆積、成長させようとすれば、得られる
シリコン薄膜は非晶質となってしまい、多結晶薄膜とす
ることは困難である。しかしながら、本発明を用いるこ
とにより、この問題は容易に解決される。すなわち、非
晶質シリコンは高速度で形成することができるので、こ
れに、本発明を適用することにより、成長速度を阻害す
る要因を排除できる。成長速度は照射光の強度にも影響
されるが、5人/秒以」二の成長速度を達成することは
容易である。Another feature of the present invention is that it can effectively increase the growth rate of polycrystalline thin films at low temperatures. In the temperature range used in the present invention, if a silicon thin film is deposited and grown at a high rate of 5 people/second or more, the resulting silicon thin film will become amorphous, and the polycrystalline thin film will become amorphous. It is difficult to do so. However, by using the present invention, this problem is easily solved. That is, since amorphous silicon can be formed at a high rate, by applying the present invention thereto, factors that inhibit the growth rate can be eliminated. Although the growth rate is also affected by the intensity of the irradiated light, it is easy to achieve a growth rate of 5 or more people/second.
本発明における非晶質シリコン薄膜の膜厚は原理的には
限定されるものではないが、実用上からは20μmのl
IU厚まで処理可能である。また、100人程0超薄膜
においても本発明は効果的であることを確認した。The thickness of the amorphous silicon thin film in the present invention is not limited in principle, but from a practical standpoint it is 20 μm.
It is possible to process up to IU thickness. Furthermore, it was confirmed that the present invention is effective even in ultra-thin films containing about 100 people.
本発明において使用する基板としては、単結晶または非
単結晶、透明または不透明の材料等特に限定されるもの
ではないが、実用上からはガラス基板が、そのなかでも
変形温度が低く耐熱性に乏しいが安価である低融点ガラ
スたる青板ガラスでさえ基板として好適に用いることが
できる。この点が本発明の最も特徴とする点であり、シ
リコンウェハを基板に用いている従来の技術と著しい対
象をなす点なのである。The substrate used in the present invention is not particularly limited, such as single-crystal or non-single-crystal, transparent or opaque materials, but from a practical standpoint, glass substrates are preferred because of their low deformation temperature and poor heat resistance. Even soda-lime glass, which is a low-melting glass that is inexpensive, can be suitably used as the substrate. This point is the most distinctive feature of the present invention, and is in marked contrast to conventional techniques that use silicon wafers as substrates.
[発明を実施するための好ましい形態]つぎに本発明の
実施の態様についてしるす。非晶質シリコン薄膜が形成
されたガラス基板をランプヒータならびに熱線ヒータに
より400〜600°Cに加熱しつつ、可視光線または
紫外線レーザーによって、照射する。可視光線はガラス
基板を透過するので、照射の方向は限定されない。非晶
質シリコンを直接またはガラスを通して間接的に照射す
ることもできる。もちろん、紫外線はガラスの吸収係数
が大きいので非晶質シリコン薄膜を直接照射することが
効果的である。[Preferred Modes for Carrying Out the Invention] Next, embodiments of the present invention will be described. The glass substrate on which the amorphous silicon thin film is formed is heated to 400 to 600° C. using a lamp heater and a hot wire heater, and irradiated with visible light or ultraviolet laser. Since visible light passes through the glass substrate, the direction of irradiation is not limited. Amorphous silicon can also be irradiated directly or indirectly through glass. Of course, since the absorption coefficient of glass is large for ultraviolet rays, it is effective to directly irradiate the amorphous silicon thin film.
[発明の効果及び産業上の利用可能性]本発明において
は、多結晶シリコン薄膜が、非品質シリコン薄膜から、
基板の温度が600°C以下と云う低温で高速度で形成
されるものである。[Effects and industrial applicability of the invention] In the present invention, the polycrystalline silicon thin film is made from a non-quality silicon thin film.
The substrate is formed at a low temperature of 600° C. or less at high speed.
本発明においては、このように、低融点のガラス基板が
利用できることから大面積の半導体装置用の材料として
有効に用いられる。とくに、太陽電池や液晶駆動用トラ
ンジスタ用に高性能でかつ安価で実用的な材料を提供す
るものである。In the present invention, since a glass substrate with a low melting point can be used, it can be effectively used as a material for a large area semiconductor device. In particular, it provides high-performance, inexpensive, and practical materials for solar cells and liquid crystal driving transistors.
[実施例1]
1μmの非晶質シリコン薄膜が形成された青板ガラスを
準備し、これをランプヒータで400°Cに加熱しつつ
、514nmのアルゴンイオンレーザ−を照射した。レ
ーザービーム径は0.2cmで非晶質シリコン上を走査
して10cm角のサイズの多結晶シリコン薄膜を得た。[Example 1] A blue plate glass on which a 1 μm thick amorphous silicon thin film was formed was prepared, and while it was heated to 400° C. with a lamp heater, it was irradiated with a 514 nm argon ion laser. A laser beam with a diameter of 0.2 cm was scanned over the amorphous silicon to obtain a polycrystalline silicon thin film with a size of 10 cm square.
走査速度は1cm/秒であり、成膜速度に換算すると2
0人/秒以上に匹敵する高速度で多結晶シリコンを得る
ことができた。この多結晶シリコン薄膜の導電率はI
Xl0−7S 7cmであり、太陽電池用の基板として
十分使用できるものであった。X線回折(XRD)によ
り推算された粒径は0.1 μmであった。The scanning speed is 1 cm/sec, which is converted to a film formation speed of 2
Polycrystalline silicon could be obtained at a high speed comparable to 0 person/second or higher. The conductivity of this polycrystalline silicon thin film is I
It was Xl0-7S 7 cm and could be sufficiently used as a substrate for solar cells. The particle size estimated by X-ray diffraction (XRD) was 0.1 μm.
[実施例2]
1μmのN型非晶質シリコンが形成された青板ガラスを
準備し、これをランプヒータで400°Cに加熱しつつ
、514nmのアルゴンイオンレーザ−を照射した。レ
ーザービーム径はQ、2cmで非晶質シリコン上を走査
して10cm角のサイズの多結晶シリコン薄膜を得た。[Example 2] A blue plate glass on which 1 μm of N-type amorphous silicon was formed was prepared, and while it was heated to 400° C. with a lamp heater, it was irradiated with a 514 nm argon ion laser. The laser beam diameter was Q and the amorphous silicon was scanned with a diameter of 2 cm to obtain a polycrystalline silicon thin film having a size of 10 cm square.
走査速度は2cm/秒であり、成膜速度に換算すると4
0人/秒以上に匹敵する高速度で多結晶シリコンを得る
ことができた。このN型多結晶シリコン薄膜の導電率は
600S/cmであり、太陽電池用の基板として十分使
用できるものであった。The scanning speed is 2 cm/sec, which is converted into a film formation speed of 4.
Polycrystalline silicon could be obtained at a high speed comparable to 0 person/second or higher. The conductivity of this N-type polycrystalline silicon thin film was 600 S/cm, and it could be sufficiently used as a substrate for solar cells.
[実施例3]
1μmのP型非晶質シリコンが形成された青板ガラス準
備し、これをランプヒータで400°Cに加熱しつつ、
514nmのアルゴンイオンレーザ−を照射した。レー
ザービーム径は0 、2cmで非晶質シリコン」二を走
査して10cm角のサイズの多結晶シリコン薄膜を得た
。走査速度は0.5cm /秒であり、成膜速度に換算
すると10/秒以上に匹敵する高速度で多結晶シリコン
を得ることができた。このP型多結晶シリコン薄膜の導
電率は300 S/cmであり、太陽電池用の基板とし
て十分使用できるものであった。[Example 3] A blue plate glass on which 1 μm of P-type amorphous silicon was formed was prepared, and while it was heated to 400°C with a lamp heater,
It was irradiated with a 514 nm argon ion laser. A polycrystalline silicon thin film having a size of 10 cm square was obtained by scanning amorphous silicon with a laser beam diameter of 0.2 cm. The scanning speed was 0.5 cm 2 /sec, and polycrystalline silicon could be obtained at a high speed equivalent to 10/sec or more when converted into a film deposition rate. The conductivity of this P-type polycrystalline silicon thin film was 300 S/cm, and it could be sufficiently used as a substrate for solar cells.
特許出願人 三井東圧化学株式会社Patent applicant: Mitsui Toatsu Chemical Co., Ltd.
Claims (4)
リコン薄膜に光を照射することを特徴とする多結晶シリ
コン薄膜の製法。(1) A method for producing a polycrystalline silicon thin film, which is characterized by irradiating light onto an amorphous silicon thin film formed on a substrate while heating the substrate.
ザーを照射する特許請求の範囲第1項記載の多結晶シリ
コン薄膜の製法。(2) The method for producing a polycrystalline silicon thin film according to claim 1, wherein the amorphous silicon thin film is irradiated with visible light or ultraviolet laser.
1項記載の多結晶シリコン薄膜の製法。(3) The method for producing a polycrystalline silicon thin film according to claim 1, wherein the substrate is a low melting point glass substrate.
囲第3項記載の多結晶シリコン薄膜の製法。(4) The method for producing a polycrystalline silicon thin film according to claim 3, wherein heating is performed at a temperature below the melting point of the glass substrate.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63019674A JP2698363B2 (en) | 1988-02-01 | 1988-02-01 | Manufacturing method of polycrystalline silicon thin film |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63019674A JP2698363B2 (en) | 1988-02-01 | 1988-02-01 | Manufacturing method of polycrystalline silicon thin film |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01196116A true JPH01196116A (en) | 1989-08-07 |
| JP2698363B2 JP2698363B2 (en) | 1998-01-19 |
Family
ID=12005782
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63019674A Expired - Fee Related JP2698363B2 (en) | 1988-02-01 | 1988-02-01 | Manufacturing method of polycrystalline silicon thin film |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2698363B2 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04288817A (en) * | 1991-03-18 | 1992-10-13 | G T C:Kk | Manufacture of polycrystalline semiconductor film |
| US5254208A (en) * | 1990-07-24 | 1993-10-19 | Semiconductor Energy Laboratory Co., Ltd. | Method for manufacturing a semiconductor device |
| US6008078A (en) * | 1990-07-24 | 1999-12-28 | Semiconductor Energy Laboratory Co., Ltd. | Method for manufacturing a semiconductor device |
| US6429483B1 (en) | 1994-06-09 | 2002-08-06 | Semiconductor Energy Laboratory Co., Ltd. | Semiconductor device and method for forming the same |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62229924A (en) * | 1986-03-31 | 1987-10-08 | Canon Inc | Method of reforming semiconductor |
-
1988
- 1988-02-01 JP JP63019674A patent/JP2698363B2/en not_active Expired - Fee Related
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62229924A (en) * | 1986-03-31 | 1987-10-08 | Canon Inc | Method of reforming semiconductor |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5254208A (en) * | 1990-07-24 | 1993-10-19 | Semiconductor Energy Laboratory Co., Ltd. | Method for manufacturing a semiconductor device |
| US5716857A (en) * | 1990-07-24 | 1998-02-10 | Semiconductor Energy Laboratory Co., Ltd. | Method for manufacturing a semiconductor device |
| US6008078A (en) * | 1990-07-24 | 1999-12-28 | Semiconductor Energy Laboratory Co., Ltd. | Method for manufacturing a semiconductor device |
| US6486495B2 (en) | 1990-07-24 | 2002-11-26 | Semiconductor Energy Laboratory Co., Ltd. | Method for manufacturing a semiconductor device |
| US7026200B2 (en) | 1990-07-24 | 2006-04-11 | Semiconductor Energy Laboratory Co. Ltd. | Method for manufacturing a semiconductor device |
| JPH04288817A (en) * | 1991-03-18 | 1992-10-13 | G T C:Kk | Manufacture of polycrystalline semiconductor film |
| US6429483B1 (en) | 1994-06-09 | 2002-08-06 | Semiconductor Energy Laboratory Co., Ltd. | Semiconductor device and method for forming the same |
| US7547915B2 (en) | 1994-06-09 | 2009-06-16 | Semiconductor Energy Laboratory Co., Ltd. | Semiconductor device having SiOxNy film |
| US8330165B2 (en) | 1994-06-09 | 2012-12-11 | Semiconductor Energy Laboratory Co., Ltd. | Semiconductor device and method for forming the same |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2698363B2 (en) | 1998-01-19 |
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