JPS5895687A - Growth of crystal granule of thin film - Google Patents
Growth of crystal granule of thin filmInfo
- Publication number
- JPS5895687A JPS5895687A JP56192543A JP19254381A JPS5895687A JP S5895687 A JPS5895687 A JP S5895687A JP 56192543 A JP56192543 A JP 56192543A JP 19254381 A JP19254381 A JP 19254381A JP S5895687 A JPS5895687 A JP S5895687A
- Authority
- JP
- Japan
- Prior art keywords
- film
- thin film
- thin
- silicon
- heated
- 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.)
- Pending
Links
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P34/00—Irradiation with electromagnetic or particle radiation of wafers, substrates or parts of devices
- H10P34/40—Irradiation with electromagnetic or particle radiation of wafers, substrates or parts of devices with high-energy radiation
- H10P34/42—Irradiation with electromagnetic or particle radiation of wafers, substrates or parts of devices with high-energy radiation with electromagnetic radiation, e.g. laser annealing
Landscapes
- Crystals, And After-Treatments Of Crystals (AREA)
- Recrystallisation Techniques (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は薄膜の結晶粒の成長または単結晶化を行う方法
に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for growing crystal grains or single crystallizing a thin film.
薄[Kレーずビームや電子ビームを照射・加熱すること
Kよ抄シリコン等の薄膜の結晶粒の成長または単結晶化
を行おうとするいわゆるビームアニール法を用−た薄膜
の結晶粒の成長もしくは単結晶化技術は、80 I (
8i1icon on In5ulator)と呼ばれ
イーる非晶質絶縁基板上に単結晶または結晶較径の大き
なシリコン薄膜を形成した構造の実現と一〇九点で多く
の人々の注目を集めている。Growth of crystal grains in thin films such as silicon by irradiating and heating them with laser beams or electron beams, or using the so-called beam annealing method to achieve single crystallization. Single crystallization technology is 80 I (
It has attracted the attention of many people for its 109 points and the realization of a structure in which a silicon thin film with a single crystal or a large crystal diameter is formed on an amorphous insulating substrate.
従来のビームアニール法を用い丸薄膜の結晶成長技術で
は、結晶成長を行わそうとする薄膜自体にレーザビーム
や電子ビームエネルギーの大部分を直接吸収させて加熱
する方式が採られていた@しかし、この様な直接加熱方
式を用いた場合には被加熱体の材料や構造が決まると、
それに応じた適切なビームの種−や照射条件の1i囲が
、自動的に決まり、ビームのm*や照射条件の自由度が
少ないとい)欠点があった。たとえば、レーザアニール
技術を用いてシリコン薄膜を単結晶化しようとする場合
、@取係数の小さい炭酸ガスレーず(波長10.4i7
1m)を用−ることは、エネルギーの利用効率という観
点必ら好ましくな―だけでなく、薄膜を通してその下地
や基板をも同時に直接加熱してしまうことにな抄、高出
力が得られる炭酸ガスレーずを有効に利用することがで
きなかつた・また、電子ビームを用いる場合においても
、加熱される薄膜の膜厚が数千A揚度以下になってくる
と、電子ビームによる発熱を主としてその薄膜内に閉じ
こめるためKは電子ビームの加速エネルギーを数ke
V以下という低−値に限定する必要が生じる。その様な
低加速領域においては、引出し電極電圧も低くしなけれ
ばならなψため、充分な電子ビーム電流密度が得難いと
いう問題が生じる。In the conventional crystal growth technology for round thin films using the beam annealing method, a method was adopted in which the thin film itself was heated by directly absorbing most of the laser beam or electron beam energy. When using such a direct heating method, once the material and structure of the heated object is determined,
The appropriate beam type and irradiation condition range are automatically determined accordingly, which has the disadvantage that there is less freedom in beam m* and irradiation conditions. For example, when trying to single-crystallize a silicon thin film using laser annealing technology, carbon dioxide laser with a small coefficient (wavelength 10.4i7)
1 m) is not only undesirable from the point of view of energy utilization efficiency, but also avoids directly heating the substrate and substrate through the thin film. In addition, even when using an electron beam, when the thickness of the thin film to be heated becomes less than several thousand amps, the heat generated by the electron beam is mainly absorbed by the thin film. In order to confine the electron beam, K reduces the acceleration energy of the electron beam to several ke.
It becomes necessary to limit the value to a low value of V or less. In such a low acceleration region, the extraction electrode voltage must also be lowered, which causes the problem that it is difficult to obtain a sufficient electron beam current density.
本発明は上記従来方法における問題点を大幅に改善し九
新規な薄膜の結晶粒成長または単結晶化を行う方法に関
するものである。The present invention significantly improves the problems of the conventional methods described above and relates to a novel method for growing crystal grains or forming single crystals in thin films.
本発明による方法は、第1の薄膜上に直!Iまたは菖2
の薄膜を介して第3の薄膜を堆積した構造に1光もしく
は電子ビームを照射することKより主として線光もしく
は電子ビーム照射によって加熱され九II3の薄膜ふも
の熱伝導によって第1の薄膜を加熱することによシ嬉1
の薄膜の結晶粒の成長を九は単結晶化を行うことを特徴
とするものである・従って、本発明による方法にお−で
は、たとえばレーザアニール法を用−る場合には、結晶
粒の成長または単結晶化を行うべき第1の薄膜の吸収係
数や反射係数といった光学的性質と無関係にレーザの種
類を決め、それに応じた表面吸収層としての第3の薄膜
の材料や膜厚を選ぶことがで吉る◎また、電子ビームア
ニール法を用いる場合には、結晶粒径を成長させるべき
lNl0薄膜の厚さに無関係に電子ビームの加速エネル
ギーを決め、それに応じ九表面吸取層としてのI!3の
薄膜の材料や膜厚を選べばよい。さもに本発明による方
法においては、第1の薄膜は主として表面吸収層として
の第3の薄膜からの熱伝導によって加熱されるので、レ
ーザや電子ビームのビームスgyF内でのミクロな強度
変動は熱拡散により平均化され、#11の薄膜の温炭分
布に与える影響が緩和されるという新たな利点も生じる
ことが判った。The method according to the present invention allows direct application of the first film onto the first thin film. I or irises 2
The structure in which the third thin film is deposited is irradiated with one light or electron beam through the thin film of K. The first thin film is heated by the heat conduction of the thin film of 9II3, which is heated mainly by line light or electron beam irradiation. I'm happy to do it 1
The growth of crystal grains in a thin film is characterized by single crystallization. Therefore, in the method according to the present invention, for example, when using a laser annealing method, the growth of crystal grains in a thin film is Decide the type of laser regardless of the optical properties such as absorption coefficient and reflection coefficient of the first thin film to be grown or single crystallized, and select the material and thickness of the third thin film as the surface absorption layer accordingly. In addition, when using the electron beam annealing method, the acceleration energy of the electron beam is determined regardless of the thickness of the lNl0 thin film whose crystal grain size is to be grown, and the I ! All you have to do is choose the material and thickness of the thin film in step 3. In the method according to the present invention, the first thin film is heated mainly by heat conduction from the third thin film as a surface absorption layer, so that microscopic intensity fluctuations within the beam gyF of the laser or electron beam are caused by heat. It has been found that a new advantage arises in that it is averaged by diffusion and the influence of #11 thin film on hot coal distribution is alleviated.
次に本発明による方法の実施例を図を用いて具体的’に
説明する。第1の実施例は、炭酸ガスレーザ照射によ)
多結晶シリコン膜の結晶粒の成長を行わせ九場合であり
、その主要1根での試料断面略図tttIN1図(−〜
(@に示す。先ず、I!1図(荀の如く、シリコン基板
llの熱酸化によ抄形成したシリコン醗化膜12上に化
学蒸着法により 5oooムの厚さの多結晶シリコン膜
13を堆積する。次に、周知のホトエツチング法および
選択酸化法等の組合せにより111図(鴫に示した様に
島状13’に多結晶シリコン領域を残して周囲を酸化膜
14に変換する。次に熱酸化により島状多結晶シリコン
領域13’の上に約500ムの薄−熱羨化膜15を形成
するC第1図化〉)。Next, embodiments of the method according to the present invention will be described in detail with reference to the drawings. The first example uses carbon dioxide laser irradiation)
This is a case in which the crystal grains of a polycrystalline silicon film are grown.
(As shown in @. First, as shown in Figure I! Next, by a combination of well-known photoetching methods and selective oxidation methods, the polycrystalline silicon region is left in an island shape 13' as shown in FIG. A thin thermally oxidized film 15 of approximately 500 μm is formed on the island-shaped polycrystalline silicon region 13' by thermal oxidation (see Figure C1).
次に、アルゴン(Ar)と酸素(0,)との混合雰囲気
中でチタン(Ti)をターゲットとして、いわゆる反応
性スパッタリングを行うことにより、第1図(山の如く
表面V&収層としての鹸化チタン膜16を約5oooム
の厚さに堆積した。次K 1000℃の酸素雰囲気中で
熱処理を行−1酸化チタン膜16の緻密化および下地の
酸化シリコン膜との密着強度の向上を図って必ら第1図
(e)に示した如く炭酸ガスレーザ光17(波長IQ、
6 Jlm)を照射した。この際、酸化チダン膜16
の炭酸ガスレーザ光に対する吸収係数は多結晶シリコン
膜1fK対するものより著して大きいため、炭酸ガスレ
ーザ光に対する良好な吸収層として作用する。従って、
多結晶シリコン膜13’は、酸化チタン膜166らの熱
伝導によ抄加熱され、その結晶粒径が数sm〜数士am
と炭酸ガスレーザ照射しない場合に比して1〜2桁増大
した。Next, by performing so-called reactive sputtering using titanium (Ti) as a target in a mixed atmosphere of argon (Ar) and oxygen (0. The titanium film 16 was deposited to a thickness of about 5 mm.Next, heat treatment was performed in an oxygen atmosphere at 1000°C to make the titanium oxide film 16 denser and to improve the adhesion strength with the underlying silicon oxide film. As shown in FIG. 1(e), the carbon dioxide laser beam 17 (wavelength IQ,
6 Jlm). At this time, the titanium oxide film 16
Since the absorption coefficient for carbon dioxide laser light is significantly larger than that for the polycrystalline silicon film 1fK, it acts as a good absorption layer for carbon dioxide laser light. Therefore,
The polycrystalline silicon film 13' is heated by thermal conduction through the titanium oxide film 166 and the like, and its crystal grain size ranges from several sm to several am.
This increased by one to two orders of magnitude compared to the case without carbon dioxide laser irradiation.
jllD実施例は、多結晶シリコン膜が単結晶シリコン
基板と一部で直接接している構造で、いわゆる1ate
rsil seeding法と呼げれているものに対応
するものである。第1の実施例の場合1同様に周知のホ
トエツチング法、選択酸化法、化学蒸着法、反応性スパ
ッタリング法等を用いて第2図に断面略図として示した
様な構造を形成する。The jllD example has a structure in which a polycrystalline silicon film is in direct contact with a single crystal silicon substrate in a part, so-called 1ate
This corresponds to what is called the Rsil seeding method. In the case of the first embodiment, a structure as shown in the schematic cross-sectional view of FIG. 2 is formed using the well-known photoetching method, selective oxidation method, chemical vapor deposition method, reactive sputtering method, etc., as in the case of the first embodiment.
ここに21はシリコン単結晶基板、22はシリコン酸化
膜、23は多結晶シリコン膜、24はシリコン酸化膜、
25は酸化チタン膜である。次に第2図の左から右の方
向に炭酸ガスレーザ光を走査させて照射するととKより
、単結晶シリコン基板21に接して―る領域2SThら
連続的に右横方向にエピタキシャル的に多結晶Vリコゾ
膜23を単結晶化することができた。Here, 21 is a silicon single crystal substrate, 22 is a silicon oxide film, 23 is a polycrystalline silicon film, 24 is a silicon oxide film,
25 is a titanium oxide film. Next, when the carbon dioxide laser beam is scanned and irradiated in the direction from left to right in FIG. The V-licozo film 23 could be made into a single crystal.
第3の実施例では、第2の実施例における炭酸ガスレー
ず照射の代bK加速エネルギー15 ke VO電子ビ
ームを用−1かつ、表面吸収層25として酸化チタンの
代ヤにスパッタリングで形成し九厚さ6000A Oチ
タン膜を用いた。また、多結晶シリコン膜23の膜厚は
30GOAであシ、酸化シリコンJII22の膜厚は5
00ムを用−九。15 ke Vの電子ビームをシリコ
ンKWA射し九場会の発熱ピーク位置は表面から約63
00ムの深さの所であるので、従来の方法の様に15k
eVO電子ビームを直接部■ムの厚さのシリコン膜に照
射すると発熱のピーク位置はシリコン膜を超え丸下地の
中になってしまう、しかし、本発明による方法を用−る
と、15keVの電子ビームのチタン中での発熱ピーク
位置は約3300ムであるので、電子ビーム照射による
発熱の大部分はチタン膜中で生じる。従って、多結晶シ
9コ>膜23は実効的にはチタン膜25からの熱伝導に
よりて加熱され、下地の酸化膜22の蟲赴シリコン膜2
3より低く抑えることがで自た〇また、今まで述べ九実
施例ではシリコン膜と酸化チタン膜あるいはシリコン膜
とチタン膜はシリコン酸化膜を介して積層していたが、
シリコン膜と酸化チタン膜の場合ならば、加熱しても互
いに度応しないので、シリコン酸化膜を介さず直接積層
することがIv能である。以上述べた様に′F地の不必
要な加熱を抑えることは、3次元集積回路等多層にデバ
イスが集積された構造において、既に形成された下層の
デバイス特性を熱的に変化させないということで、極め
て重要である。In the third embodiment, an electron beam with acceleration energy of 15 ke VO was used for the carbon dioxide laser beam irradiation in the second embodiment, and a surface absorption layer 25 was formed by sputtering on titanium oxide with a thickness of 9. A 6000A titanium film was used. Further, the film thickness of the polycrystalline silicon film 23 is 30 GOA, and the film thickness of the silicon oxide JII 22 is 5 GOA.
Use 00mu-9. When a 15 ke V electron beam was irradiated onto the silicon KWA, the heat generation peak position of Kuba-kai was approximately 63 mm from the surface.
Since it is at a depth of 0.00 m, it is necessary to
When an eVO electron beam is directly irradiated onto a silicon film with a thickness of 1.5 keV, the peak position of heat generation exceeds the silicon film and becomes inside the base.However, when the method of the present invention is used, the 15 keV electron Since the heat generation peak position of the beam in titanium is about 3300 μm, most of the heat generated by electron beam irradiation occurs in the titanium film. Therefore, the polycrystalline silicon film 23 is effectively heated by heat conduction from the titanium film 25, and the silicon film 23 of the underlying oxide film 22 is heated.
In addition, in the nine embodiments described so far, the silicon film and the titanium oxide film or the silicon film and the titanium film were laminated with the silicon oxide film interposed in between.
In the case of a silicon film and a titanium oxide film, they do not interact with each other even when heated, so it is possible to directly stack them without using a silicon oxide film. As mentioned above, suppressing unnecessary heating of the 'F' ground means not thermally changing the device characteristics of the lower layer that has already been formed in a structure where devices are integrated in multiple layers, such as a three-dimensional integrated circuit. , is extremely important.
第1〜2図は、本発明による方法の実施例における主要
工程での素子断面略図。
11.21・−・・・・・・シリコン基板、12.14
.15.22.24−・・・・・・・・−一酸化シリコ
ン% 13. la;23・・・・−・多結晶シリコン
、16−−−−−−・酸化チタン、17・−・・・・−
炭酸ガスレーザビーム25−・・・−・・・酸化チタン
またはチタン、2t・甲jp扇晶シリコン威、μ゛ンシ
コン差板と捗丁り傾城。
も1図
(ル)1 and 2 are schematic cross-sectional views of elements at main steps in an embodiment of the method according to the present invention. 11.21 --- Silicon substrate, 12.14
.. 15.22.24--Silicon monoxide% 13. la; 23·······Polycrystalline silicon, 16········Titanium oxide, 17········
Carbon dioxide laser beam 25-------Titanium oxide or titanium, 2t/A fan crystal silicon, micro-insulator difference plate and tilting. Figure 1 (le)
Claims (1)
の薄膜を堆積した構造に1光鬼しくは電子ビームを照射
することにより、主として該光もしくは電子ビーム照射
によって加熱された第3の薄膜ふらの熱伝導によってI
llの薄膜を加熱するととKよ9第1の薄膜の結晶粒の
成長または単結晶化を行うことを特徴とする薄膜の結晶
粒成長方法。Directly on the thin film of III or! 3rd through 12 thin films
By irradiating a structure with a thin film deposited with a single light or electron beam, I
A method for growing crystal grains in a thin film, characterized in that when the thin film of 11 is heated, the crystal grains of the first thin film grow or become single crystallized.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56192543A JPS5895687A (en) | 1981-11-30 | 1981-11-30 | Growth of crystal granule of thin film |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56192543A JPS5895687A (en) | 1981-11-30 | 1981-11-30 | Growth of crystal granule of thin film |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS5895687A true JPS5895687A (en) | 1983-06-07 |
Family
ID=16293021
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56192543A Pending JPS5895687A (en) | 1981-11-30 | 1981-11-30 | Growth of crystal granule of thin film |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5895687A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6054426A (en) * | 1983-09-05 | 1985-03-28 | Agency Of Ind Science & Technol | Manufacture of semiconductor thin film crystal layer |
| JPS60105219A (en) * | 1983-11-14 | 1985-06-10 | Agency Of Ind Science & Technol | Manufacture of semiconductor thin film crystal layer |
-
1981
- 1981-11-30 JP JP56192543A patent/JPS5895687A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6054426A (en) * | 1983-09-05 | 1985-03-28 | Agency Of Ind Science & Technol | Manufacture of semiconductor thin film crystal layer |
| JPS60105219A (en) * | 1983-11-14 | 1985-06-10 | Agency Of Ind Science & Technol | Manufacture of semiconductor thin film crystal layer |
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