JP2811763B2 - Method for manufacturing insulated gate field effect transistor - Google Patents
Method for manufacturing insulated gate field effect transistorInfo
- Publication number
- JP2811763B2 JP2811763B2 JP17232889A JP17232889A JP2811763B2 JP 2811763 B2 JP2811763 B2 JP 2811763B2 JP 17232889 A JP17232889 A JP 17232889A JP 17232889 A JP17232889 A JP 17232889A JP 2811763 B2 JP2811763 B2 JP 2811763B2
- Authority
- JP
- Japan
- Prior art keywords
- film
- temperature
- gas
- effect transistor
- insulated gate
- 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.)
- Expired - Fee Related
Links
- 238000000034 method Methods 0.000 title claims description 37
- 230000005669 field effect Effects 0.000 title claims description 17
- 238000004519 manufacturing process Methods 0.000 title claims description 14
- 239000007789 gas Substances 0.000 claims description 31
- 239000004065 semiconductor Substances 0.000 claims description 18
- 230000000694 effects Effects 0.000 claims description 15
- 238000004544 sputter deposition Methods 0.000 claims description 14
- 239000013078 crystal Substances 0.000 claims description 12
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 6
- 239000001307 helium Substances 0.000 claims description 5
- 229910052734 helium Inorganic materials 0.000 claims description 5
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 claims description 5
- 230000005684 electric field Effects 0.000 claims description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 3
- 229910052786 argon Inorganic materials 0.000 claims description 3
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 2
- 239000010408 film Substances 0.000 description 81
- 238000010438 heat treatment Methods 0.000 description 22
- 239000010410 layer Substances 0.000 description 19
- 239000000758 substrate Substances 0.000 description 19
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 16
- 238000000137 annealing Methods 0.000 description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 11
- 239000001257 hydrogen Substances 0.000 description 10
- 229910052739 hydrogen Inorganic materials 0.000 description 10
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 8
- 229910021417 amorphous silicon Inorganic materials 0.000 description 8
- 229910052710 silicon Inorganic materials 0.000 description 8
- 239000010703 silicon Substances 0.000 description 8
- 229910004298 SiO 2 Inorganic materials 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 7
- 239000012535 impurity Substances 0.000 description 7
- 239000011521 glass Substances 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 239000011229 interlayer Substances 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 238000002425 crystallisation Methods 0.000 description 4
- 230000008025 crystallization Effects 0.000 description 4
- 230000007547 defect Effects 0.000 description 4
- 150000002500 ions Chemical class 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000005268 plasma chemical vapour deposition Methods 0.000 description 4
- 239000007790 solid phase Substances 0.000 description 4
- 239000002344 surface layer Substances 0.000 description 4
- 238000005229 chemical vapour deposition Methods 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 238000005468 ion implantation Methods 0.000 description 3
- 238000004518 low pressure chemical vapour deposition Methods 0.000 description 3
- 229910021424 microcrystalline silicon Inorganic materials 0.000 description 3
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000003795 desorption Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 239000004973 liquid crystal related substance Substances 0.000 description 2
- 229910021421 monocrystalline silicon Inorganic materials 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 238000005036 potential barrier Methods 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 238000005224 laser annealing Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000002161 passivation Methods 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Electrodes Of Semiconductors (AREA)
- Thin Film Transistor (AREA)
- Insulated Gate Type Field-Effect Transistor (AREA)
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に係わり、特に絶縁
ゲート型電界効果トランジスタのゲート絶縁膜の形成方
法に関する。The present invention relates to a method for manufacturing a semiconductor device, and more particularly to a method for forming a gate insulating film of an insulated gate field effect transistor.
[従来の技術] 近年、三次元ICや、大型で高解像度の液晶表示パネル
や、高速で高解像度の密着型イメージセンサ等へのニー
ズが高まるにつれて、低温で良質のゲート絶縁膜を形成
する技術が重要となってきた。熱酸化法は、900〜1200
℃程度の高温プロセスであるため、(1)安価なガラス
基板上に素子を形成できない。(2)三次元ICでは下層
部の素子に悪影響(不純物の拡散等)を与える等の問題
があり、CVD法等で低温で酸化膜を形成する技術の検討
が進められている。[Prior art] In recent years, as the need for three-dimensional ICs, large, high-resolution liquid crystal display panels, and high-speed, high-resolution contact-type image sensors has increased, technology for forming high-quality gate insulating films at low temperatures has been increasing. Has become important. The thermal oxidation method is 900-1200
(1) An element cannot be formed on an inexpensive glass substrate. (2) The three-dimensional IC has a problem of giving an adverse effect (diffusion of impurities, etc.) to an element in a lower layer portion, and a technique for forming an oxide film at a low temperature by a CVD method or the like is being studied.
[発明が解決しようとする課題] ところが、CVD法で形成した酸化膜は、ゲート絶縁耐
圧、界面準位密度が高い等の問題があり、実用レベルの
素子を安定して形成することが困難であった。そこで本
発明はこの様な問題点を解決するものであり、その目的
とするところは、ゲート絶縁耐圧が高く、界面準位密度
が低い絶縁ゲート型電界効果トランジスタ用のゲート絶
縁膜の形成方法を提供するところにある。[Problems to be Solved by the Invention] However, the oxide film formed by the CVD method has problems such as a high gate dielectric strength and a high interface state density, and it is difficult to stably form a practical-level element. there were. Accordingly, the present invention is to solve such a problem, and an object of the present invention is to provide a method for forming a gate insulating film for an insulated gate field effect transistor having a high gate withstand voltage and a low interface state density. To provide.
[課題を解決するための手段] 本発明は、絶縁ゲート型電界効果トランジスタの製造
方法において、 少なくともアルゴンガスとヘリウムガスを含むガス槽
内に導入して、スパッタ法によりシリコン酸化膜からな
るゲート絶縁膜を形成することを特徴とする。[Means for Solving the Problems] The present invention relates to a method of manufacturing an insulated gate field effect transistor, which comprises introducing a gate insulating film made of a silicon oxide film by sputtering into a gas tank containing at least argon gas and helium gas. The method is characterized in that a film is formed.
本発明の絶縁ゲート型電界効果トランジスタの製造方
法は、前記ヘリウムガスの濃度が5%以上であることを
特徴とする。In the method of manufacturing an insulated gate field effect transistor according to the present invention, the concentration of the helium gas is 5% or more.
本発明の絶縁ゲート型電界効果トランジスタの製造方
法は、前記ゲート絶縁膜が、前記槽内の内圧が1.0Pa未
満で形成されることを特徴とする。In the method for manufacturing an insulated gate field effect transistor according to the present invention, the gate insulating film is formed such that an internal pressure in the tank is less than 1.0 Pa.
本発明の絶縁ゲート型電界効果トランジスタの製造方
法は、前記絶縁ゲート型電界効果トランジスタのチャン
ネル領域の少なくとも一部が非単結晶半導体であること
を特徴とする。The method of manufacturing an insulated gate field effect transistor according to the present invention is characterized in that at least a part of a channel region of the insulated gate field effect transistor is a non-single-crystal semiconductor.
[実施例] 第1図は、本発明の実施例における半導体装置の製造
工程図の一例である。尚、第1図では半導体素子として
薄膜トランジスタ(TFT)を形成する場合を例としてい
る。Embodiment FIG. 1 is an example of a manufacturing process diagram of a semiconductor device according to an embodiment of the present invention. FIG. 1 shows an example in which a thin film transistor (TFT) is formed as a semiconductor element.
第1図において、(a)は、ガラス、石英等の絶縁性
非晶質基板、もしくはSiO2等の絶縁性非晶質材料層等の
絶縁性非晶質材料101上にシリコン層102を形成する工程
である。成膜条件の一例としては、LPCVD法で500℃〜56
0℃程度で膜厚100Å〜2000Å程度のシリコン膜を形成す
る等の方法、プラズマCVD法で基板温度を室温〜600℃程
度に保持し、モノシラン若しくはモノシランを水素、ア
ルゴン、ヘリウム等で希釈したガスを反応室内に導入
し、高周波エネルギー等を加えガスを分解して所望の基
板上にシリコン層を膜厚100Å〜2000Å程度形成する等
の方法がある。ただし、成膜方法はこれに限定されるも
のではなく、例えば、スパッタ法、蒸着法、EB蒸着法、
MBE法等で非晶質シリコン、若しくは微結晶シリコンを
形成する方法がある。In FIG. 1, (a) shows a silicon layer 102 formed on an insulating amorphous material 101 such as an insulating amorphous substrate such as glass or quartz or an insulating amorphous material layer such as SiO 2. This is the step of performing As an example of the film forming conditions, 500 ° C. to 56 ° C. by the LPCVD method
A method of forming a silicon film with a thickness of about 100 to 2000 mm at about 0 ° C., a gas obtained by diluting monosilane or monosilane with hydrogen, argon, helium, etc. while maintaining the substrate temperature at room temperature to about 600 ° C. by a plasma CVD method. Is introduced into a reaction chamber, and high-frequency energy or the like is applied to decompose the gas to form a silicon layer on a desired substrate with a thickness of about 100 to 2000 mm. However, the film formation method is not limited to this, for example, a sputtering method, an evaporation method, an EB evaporation method,
There is a method of forming amorphous silicon or microcrystalline silicon by MBE or the like.
第1図(b)は、該シリコン層102を熱処理等により
結晶成長させる工程である。熱処理条件は、工程(a)
のシリコン層の成膜方法によってその最適条件が異な
る。FIG. 1 (b) shows a step of crystal growth of the silicon layer 102 by heat treatment or the like. The heat treatment conditions include the step (a)
The optimum conditions differ depending on the method of forming the silicon layer.
例えば、LPCVD法で成膜した場合は、550℃〜650℃程
度で2〜50時間程度窒素もしくはAr等の不活性ガス雰囲
気中で熱処理することで多結晶シリコン層103が形成さ
れる。For example, when the film is formed by the LPCVD method, the polycrystalline silicon layer 103 is formed by performing a heat treatment at about 550 ° C. to 650 ° C. for about 2 to 50 hours in an atmosphere of an inert gas such as nitrogen or Ar.
又、プラズマCVD法で形成した場合は、例えば、成膜
時の基板温度によって以下に述べるような違いがある。Further, when the film is formed by the plasma CVD method, for example, there is a difference as described below depending on the substrate temperature at the time of film formation.
(1)基板温度が室温〜150℃程度の比較的低温で成膜
した膜は、膜中に多量の水素を含む非晶質シリコンにな
るが、200〜300℃程度で成膜した膜と比べてより低温の
熱処理で膜中の水素を抜くことが出来る。熱処理条件の
一例を以下に述べる。プラズマCVD反応室内で成膜後の
非晶質シリコン膜に第一のアニールを行う。成膜温度が
低い非晶質シリコン膜はポーラスな膜であるため、成膜
後そのまま大気中に取り出すと膜中に酸素等が取り込ま
れ易く、膜質低下の原因となるが、大気中に取り出す前
に適切な熱処理を行うと膜の緻密化が成され、酸素等の
取り込みが防止される。熱処理温度は300℃以上が望ま
しく、400〜500℃程度まで温度を上げると特に効果が大
きい。尚、熱処理温度が300℃未満であっても熱処理に
よる膜の緻密化の効果はある。但し、真空を破らずに連
続してアニールを行う場合は第一のアニールを省くこと
もできる。(1) A film formed at a relatively low substrate temperature of about room temperature to about 150 ° C becomes amorphous silicon containing a large amount of hydrogen in the film, but compared with a film formed at about 200 to 300 ° C. Thus, hydrogen in the film can be removed by heat treatment at a lower temperature. An example of the heat treatment condition is described below. First annealing is performed on the formed amorphous silicon film in the plasma CVD reaction chamber. Since an amorphous silicon film having a low film formation temperature is a porous film, if the film is taken out to the atmosphere as it is after film formation, oxygen and the like are easily taken into the film, which causes a deterioration in film quality. When the heat treatment is performed appropriately, the film is densified, and the incorporation of oxygen and the like is prevented. The heat treatment temperature is desirably 300 ° C. or higher, and increasing the temperature to about 400 to 500 ° C. is particularly effective. Even if the heat treatment temperature is lower than 300 ° C., there is an effect of densification of the film by the heat treatment. However, if annealing is performed continuously without breaking vacuum, the first annealing can be omitted.
続いて、第二のアニールを行う。低い成膜温度で形成
された非晶質シリコン膜は550℃〜650℃程度の比較的低
温の熱処理を数時間〜20時間程度行なうと、水素の脱離
と結晶成長が起こり、結晶粒径1〜2μm程度の大粒径
の多結晶シリコンが形成される。尚、第一のアニール及
び第二のアニールとも所定のアニール温度まで昇温する
際に短時間で急激に温度を上昇させるのは好ましくな
い。その理由は、温度を上昇するにつれて(特に、300
℃を越えると)膜中の水素の脱離が起こり、昇温速度が
急激であると膜中に欠陥を形成し易くなる。場合によっ
てはピンホールができたり、膜が剥離することもある。
少なくとも300℃以上の温度では20℃/分よりも遅い昇
温速度(5℃/分よりも遅い昇温速度が特に望ましい)
で温度を徐々に上昇すると膜中の欠陥は少なくなる。
尚、昇温方法の詳細は後述する。Subsequently, a second annealing is performed. When a relatively low-temperature heat treatment at about 550 ° C. to 650 ° C. is performed for several hours to about 20 hours, desorption of hydrogen and crystal growth occur in an amorphous silicon film formed at a low film formation temperature, and a crystal grain size of 1 Polycrystalline silicon having a large grain size of about 2 μm is formed. In addition, it is not preferable that both the first annealing and the second annealing rapidly increase the temperature in a short time when the temperature is increased to a predetermined annealing temperature. The reason is that as the temperature increases (especially 300
When the temperature rises rapidly, defects are easily formed in the film. In some cases, pinholes are formed or the film is peeled off.
At a temperature of at least 300 ° C. or higher, a heating rate lower than 20 ° C./min (a heating rate lower than 5 ° C./min is particularly desirable)
When the temperature is gradually raised in step (b), the number of defects in the film decreases.
The details of the heating method will be described later.
(2)基板温度が150℃〜300℃程度で成膜した膜は、上
述の低温で形成した非晶質シリコン膜に比べて、膜中の
水素量は減少するが水素が脱離する温度はより高温側に
シフトする。ただし、成膜後の膜は低温で形成した膜に
比べて緻密であるため上述の第一のアニールを省くこと
もできる。第二のアニール条件は、550〜650℃程度の熱
処理を数時間〜40時間程度行うと、水素の脱離と結晶成
長が起こり、結晶粒径1〜2μmの大粒径の多結晶シリ
コンが形成される。尚、550℃〜650℃までの昇温方法の
詳細は後述するが、(1)の場合と同様に少なくとも30
0℃以上の温度では20℃/分(望ましくは、5℃/分)
よりも遅い昇温速度で温度を徐々に上昇すると膜中の欠
陥が少なくなり望ましい。(2) The film formed at a substrate temperature of about 150 ° C. to 300 ° C. has a reduced amount of hydrogen in the film but has a lower temperature at which hydrogen is desorbed than the amorphous silicon film formed at a low temperature. Shift to higher temperature. However, since the film after film formation is denser than a film formed at a low temperature, the first annealing described above can be omitted. The second annealing condition is that when a heat treatment at about 550 to 650 ° C. is performed for several hours to about 40 hours, desorption of hydrogen and crystal growth occur, and polycrystalline silicon having a large grain size of 1 to 2 μm is formed. Is done. The details of the method of raising the temperature from 550 ° C. to 650 ° C. will be described later, but at least 30 ° C. as in (1).
20 ° C / min (preferably 5 ° C / min) at temperatures above 0 ° C
It is desirable to gradually increase the temperature at a slower rate of temperature increase because the number of defects in the film is reduced.
(3)基板温度が300℃を越えると膜中の水素量はさら
に減少するが、550℃〜650℃程度のアニールでは水素の
脱離が起こり難くなるため、前記温度よりもより高い温
度での熱処理が重要となる。尚、基板温度が500℃程度
以上で形成した膜を固相成長した場合は、<110>もし
くは<100>に配向した多結晶シリコンが得られる為、T
FTの界面準位密度の低減や電界効果移動度の向上等の効
果がある。(3) When the substrate temperature exceeds 300 ° C., the amount of hydrogen in the film further decreases, but the annealing at about 550 ° C. to 650 ° C. makes it difficult for hydrogen to be desorbed. Heat treatment is important. When a film formed at a substrate temperature of about 500 ° C. or higher is subjected to solid phase growth, polycrystalline silicon oriented in <110> or <100> is obtained.
There are effects such as reduction of the interface state density of FT and improvement of field effect mobility.
第1図(c)は、工程(b)より高い所定の熱処理温
度で該多結晶シリコン層103を熱処理する工程である。
尚、工程(c)は、省くこともできるが、結晶化率を向
上させる為に、重要な工程である。工程(b)で固相成
長法で結晶成長させた多結晶シリコン層103の結晶化率
は必ずしも高くない。特に、LPCVD法で500℃〜560℃程
度の比較的低温で形成したシリコン膜(非晶質シリコ
ン、若しくは非晶質相中に微少な結晶領域が存在する微
結晶シリコンになっている。)を熱処理で固相成長させ
た場合は、その結晶化率は、50%〜70%程度と低い。そ
こで、工程(c)で工程(b)より高い温度で熱処理す
ることで、該多結晶シリコン層の未結晶化領域を結晶化
させる工程を設けることが重要となる。その結果、結晶
化率を99%以上に高めることができる。熱処理温度とし
ては、700℃〜1200℃程度の間に最適値が存在する。但
し、基板としてガラスを用いた場合は、上述のような高
温にさらすことはできないため、エキシマレーザ等の短
波長光を照射することで半導体の表面層近傍のみを上述
の温度まで昇温させ、半導体層と基板界面近傍は600℃
程度以下になるように、照射強度及び照射時間を最適化
することが重要である。一例としては、XeClエキシマレ
ーザ(波長308nm)を用い、照射強度0.1〜1.0J/cm2程度
で1〜10パルス(1パルス数+ns)照射する等の条件が
上述の条件を満たす。尚、レーザを照射した際、半導体
層と基板の界面が600℃程度以下であれば、半導体層の
表面を溶融させる条件の方が、半導体表面層の結晶性が
良好となり好ましい。特に、該表面層は反転層が形成さ
れる領域であるため、表面層の結晶性向上は、トランジ
スタ特性の向上につながる。その他の熱処理方法として
は、アニール炉で窒素若しくはAr等の不活性ガス雰囲気
中で、例えば850℃ならば1時間程度、1000℃ならば10
〜20分程度熱処理する方法、ハロゲンランプ・アークラ
ンプ・赤外線ランプ・キセノンランプ・水銀ランプ等を
用いたランプアニール、Arレーザ・He−Neレーザ等を用
いたレーザアニール等もある。FIG. 1C shows a step of heat-treating the polycrystalline silicon layer 103 at a predetermined heat treatment temperature higher than that of the step (b).
Although step (c) can be omitted, it is an important step to improve the crystallization rate. The crystallization ratio of the polycrystalline silicon layer 103 grown by the solid phase growth method in the step (b) is not always high. In particular, a silicon film formed of LPCVD at a relatively low temperature of about 500 ° C. to 560 ° C. (amorphous silicon or microcrystalline silicon in which a fine crystal region exists in an amorphous phase). When solid phase growth is performed by heat treatment, the crystallization ratio is as low as about 50% to 70%. Therefore, it is important to provide a step of crystallizing an uncrystallized region of the polycrystalline silicon layer by performing a heat treatment at a higher temperature in the step (c) than in the step (b). As a result, the crystallization rate can be increased to 99% or more. As the heat treatment temperature, an optimum value exists between about 700 ° C. and 1200 ° C. However, when glass is used as the substrate, since it is not possible to expose to the above-mentioned high temperature, only the vicinity of the semiconductor surface layer is heated to the above-described temperature by irradiating short wavelength light such as an excimer laser, 600 ° C near the interface between the semiconductor layer and the substrate
It is important to optimize the irradiation intensity and irradiation time so as to be less than the degree. As an example, conditions such as irradiation of 1 to 10 pulses (1 pulse number + ns) at an irradiation intensity of about 0.1 to 1.0 J / cm 2 using a XeCl excimer laser (wavelength 308 nm) satisfy the above-described conditions. If the interface between the semiconductor layer and the substrate is about 600 ° C. or less when laser irradiation is performed, the condition for melting the surface of the semiconductor layer is preferable because the crystallinity of the semiconductor surface layer becomes better. In particular, since the surface layer is a region where the inversion layer is formed, improvement in crystallinity of the surface layer leads to improvement in transistor characteristics. As another heat treatment method, for example, about 1 hour at 850 ° C. or 10 hours at 1000 ° C. in an inert gas atmosphere such as nitrogen or Ar in an annealing furnace.
There is also a method of performing heat treatment for about 20 minutes, a lamp annealing using a halogen lamp, an arc lamp, an infrared lamp, a xenon lamp, a mercury lamp, a laser annealing using an Ar laser, a He-Ne laser, or the like.
第1図(d)は、ゲート絶縁膜104をスパッタ法で形
成する工程である。Arガスのみでスパッタした場合は、
酸化膜の絶縁耐圧が低く、Si/SiO2の界面準位密度も低
い。しかし、Arガスに加えて、Heガスを導入すること
で、上述の問題を解決できることが、我々の検討の結果
明らかとなった。成膜方法の一例としては、ArガスとHe
ガスを真空槽内に導入して、SiO2をターゲットとし、ス
パッタさせる方法がある。混合ガス中のHeガスの濃度は
5%以上でダメージ低減の効果が現れ、10%以上でその
効果が顕著に現れ、実用的には10%〜50%程度が望まし
い。(50%以上ではダメージ低減の効果が飽和し、さら
に、スパッタレイトが低下するため。)又、スパッタ時
の内圧もダメージの低減と重要な関係がある。即ち、内
圧を下げるほど、ダメージが低減する傾向があり、2.0P
a未満でダメージ低減の効果が現れはじめ、特に、1.0Pa
未満でダメージ低減の効果が顕著になる。FIG. 1D shows a step of forming the gate insulating film 104 by a sputtering method. When sputtering with only Ar gas,
The dielectric strength of the oxide film is low, and the interface state density of Si / SiO 2 is also low. However, as a result of our investigation, it has been clarified that the above problem can be solved by introducing He gas in addition to Ar gas. As an example of the film formation method, Ar gas and He
There is a method in which a gas is introduced into a vacuum chamber and sputtering is performed using SiO 2 as a target. When the concentration of the He gas in the mixed gas is 5% or more, the effect of reducing the damage appears, and when the concentration is 10% or more, the effect becomes remarkable. Practically, about 10% to 50% is desirable. (If it is 50% or more, the effect of reducing the damage is saturated, and the sputter rate is further reduced.) Further, the internal pressure at the time of sputtering also has an important relationship with the reduction of the damage. In other words, the lower the internal pressure, the more the damage tends to decrease.
The effect of damage reduction begins to appear below a, especially at 1.0 Pa
At less than this, the effect of reducing the damage becomes remarkable.
尚、真空槽内に導入するガスは、Arガス、Heガスの他
に、酸素等を混入してもよい。また、ターゲットとし
て、SiO2の代わりにSiを用い、Arガス、Heガス、酸素ガ
ス等を真空槽内に導入し、酸化膜を形成する方法もあ
る。また、Heガスの代わりに、Neガスを用いても、Heガ
スと同様の効果があるが、Heガスを用いたほうが良質の
酸化膜が得られた。The gas introduced into the vacuum chamber may contain oxygen and the like in addition to Ar gas and He gas. There is also a method of forming an oxide film by using Si instead of SiO 2 as a target and introducing an Ar gas, a He gas, an oxygen gas or the like into a vacuum chamber. In addition, even if Ne gas is used instead of He gas, the same effect as that of He gas is obtained. However, a higher quality oxide film is obtained by using He gas.
また、酸化膜を形成する前に、真空槽内に少なくとも
水素ガスを含むガスを導入し、シリコン層102上の自然
酸化膜を、水素プラズマに曝すことで除去する手段も有
効である。この場合、(1)基板温度が室温から300℃
程度の低温で自然酸化膜を除去できる。(2)自然酸化
膜を除去した後、真空を破らずに連続してゲート絶縁膜
を形成できる。等のメリットがあり、Si/SiO2の界面準
位を低減する効果がある。In addition, it is also effective to introduce a gas containing at least hydrogen gas into the vacuum chamber and remove the natural oxide film on the silicon layer 102 by exposing it to hydrogen plasma before forming the oxide film. In this case, (1) the substrate temperature is from room temperature to 300 ° C.
The natural oxide film can be removed at a low temperature. (2) After removing the natural oxide film, a gate insulating film can be formed continuously without breaking vacuum. This has the effect of reducing the interface state of Si / SiO 2 .
第1図(e)は、半導体素子を形成する工程である。
尚、第1図(e)では、半導体素子としてTFTを形成す
る場合を例としている。図において、104はゲート絶縁
膜、105はゲート電極、106はソース・ドレイン領域、10
7は層間絶縁膜、108はコンタクト穴、109は配線を示
す。TFT形成法の一例としては、ゲート電極を形成後、
ソース・ドレイン領域をイオン注入法、熱拡散法、プラ
ズマド ーピング法、イオンシャワードーピング法等で形成し、
層間絶縁膜をCVD法、スパッタ法、プラズマCVD法等で形
成する。さらに、該層間絶縁膜にコンタクト穴を開け、
配線を形成することでTFTが形成される。基板としてガ
ラスを用いた場合のソース・ドレイン領域の形成方法
は、イオン注入法でB、P等の不純物を打ち込んだ後、
600℃程度の低温で数時間〜数十時間熱処理することで
不純物の活性化を行う方法の他、イオンシャワードーピ
ング法、プラズマドーピング法等が有効である。FIG. 1 (e) shows a step of forming a semiconductor element.
FIG. 1E shows an example in which a TFT is formed as a semiconductor element. In the figure, 104 is a gate insulating film, 105 is a gate electrode, 106 is a source / drain region, 10
7 is an interlayer insulating film, 108 is a contact hole, and 109 is a wiring. As an example of a TFT forming method, after forming a gate electrode,
Source / drain regions are formed by ion implantation, thermal diffusion, plasma doping, ion shower doping, etc.
An interlayer insulating film is formed by a CVD method, a sputtering method, a plasma CVD method, or the like. Further, a contact hole is formed in the interlayer insulating film,
The TFT is formed by forming the wiring. When glass is used as a substrate, a source / drain region is formed by implanting impurities such as B and P by ion implantation,
An ion shower doping method, a plasma doping method, and the like are effective in addition to a method of activating impurities by performing a heat treatment at a low temperature of about 600 ° C. for several hours to several tens hours.
本発明は、従来の熱酸化法に代わり、スパッタ法で低
温で良質の酸化膜を形成できる点が重要である。以下に
その詳細を述べる。SiO2をターゲットとしてArガスでス
パッタする従来の方法では、前述の通り絶縁耐圧が低
く、Si/SiO2界面準位密度が高く、実用レベルの酸化膜
を形成することができなかった。Arイオンが基板表面に
入射したことによるダメージが、その原因の一つと考え
られる。そこで、基板表面に入射するArイオン数、エネ
ルギー等を低減する手段が必須となる。Arガスに加えて
Heガスを導入することで、上述のダメージが低減され、
絶縁耐圧、界面準位密度とも熱酸化膜と同等以上の特性
が得られることを確認した。特に、多結晶シリコン上で
は、熱酸化膜(絶縁耐圧3〜4MV/cm程度)よりも絶縁耐
圧が向上し、7〜8MV/cm程度になることが明らかとなっ
た。その原因は、多結晶シリコンを熱酸化した場合は、
結晶粒界に沿って酸化が進み易いため、酸化膜が突起状
になり電界集中が起こり易い。一方、スパッタ法で酸化
膜を低温形成した場合は、結晶粒界に沿った酸素の拡散
がほとんどなく、上述のような電界集中が起こり難いた
め、絶縁耐圧が向上するものと考えられる。更に、結晶
粒界に沿った酸化は、結晶粒界部に高い電位障壁を形成
するため、TFTの電界効果移動度を低下させる原因とも
なっていたが、本発明のスパッタ法による酸化膜を用い
た場合は、結晶粒界部に沿った酸素の拡散が殆ど無く、
粒界部の電位障壁を低くできる為、電界効果移動度が大
きく向上するという効果もある。The present invention is important in that a high-quality oxide film can be formed at a low temperature by a sputtering method instead of the conventional thermal oxidation method. The details are described below. In the conventional method of sputtering with Ar gas using SiO 2 as a target, as described above, the withstand voltage was low, the Si / SiO 2 interface state density was high, and a practical level oxide film could not be formed. Damage caused by Ar ions incident on the substrate surface is considered to be one of the causes. Therefore, means for reducing the number of Ar ions, energy, and the like incident on the substrate surface is essential. In addition to Ar gas
By introducing He gas, the above-mentioned damage is reduced,
It has been confirmed that characteristics that are equal to or higher than those of the thermal oxide film can be obtained in both the withstand voltage and the interface state density. In particular, it has been clarified that the dielectric strength on polycrystalline silicon is higher than that of a thermal oxide film (dielectric strength 3-4 MV / cm), and is about 7-8 MV / cm. The cause is that when polycrystalline silicon is thermally oxidized,
Oxidation easily proceeds along the crystal grain boundaries, so that the oxide film becomes protruding and electric field concentration tends to occur. On the other hand, when an oxide film is formed at a low temperature by a sputtering method, oxygen is hardly diffused along the crystal grain boundaries, and the above-described electric field concentration is unlikely to occur. Furthermore, the oxidation along the crystal grain boundaries forms a high potential barrier at the crystal grain boundaries, thus causing a reduction in the field-effect mobility of the TFT, but using an oxide film formed by the sputtering method of the present invention. In the case, there is almost no diffusion of oxygen along the grain boundary,
Since the potential barrier at the grain boundary can be lowered, there is also an effect that the field effect mobility is greatly improved.
又、本発明に基づくスパッタ法による酸化膜は、300
℃程度以下の低温で成膜できるため、安価なガラス基板
を用いた低温プロセスに応用することもできる。The oxide film formed by the sputtering method according to the present invention has a thickness of 300
Since the film can be formed at a low temperature of about ° C or less, it can be applied to a low-temperature process using an inexpensive glass substrate.
本発明に基づく半導体装置の製造方法を用い、低温プ
ロセスで形成した多結晶シリコンTFT(Nチャンネル)
の電界効果移動度は、200〜250cm2/V・sec程度であり熱
酸化法で形成したTFTよりも優れた特性が得られた。Polycrystalline silicon TFT (N-channel) formed by a low-temperature process using the semiconductor device manufacturing method according to the present invention
Has a field-effect mobility of about 200 to 250 cm 2 / V · sec, which is superior to TFT formed by thermal oxidation.
さらに、前記TFT製造工程に水素ガスもしくはアンモ
ニアガスを少なくとも含む気体のプラズマ雰囲気に半導
体素子をさらす工程等を設け、前記TFTを水素化する
と、結晶粒界に存在する欠陥密度が低減され、前記電界
効果移動度はさらに向上する。Further, a step of exposing the semiconductor element to a plasma atmosphere of a gas containing at least hydrogen gas or ammonia gas is provided in the TFT manufacturing step, and when the TFT is hydrogenated, a defect density existing at a crystal grain boundary is reduced, and the electric field is reduced. The effect mobility is further improved.
また、チャンネル領域に不純物をドーピングして、Vt
h(しきい値電圧)を制御する手段も極めて有効であ
る。固相成長法で形成した多結晶シリコンTFTでは、N
チャンネルトランジスタがデプレッション方向にVthが
シフトし、Pチャンネルトランジスタがエンハンスメン
ト方向にシャフトする傾向がある。又、上記TFTを水素
化した場合、その傾向がより顕著になる。そこで、チャ
ンネル領域に1015〜1019/cm3程度の不純物をドープする
と、Vthのシフトを抑えることができる。例えば、第1
図において、ゲート電極を形成する前に、イオン注入法
等でB(ボロン)等の不純物を1011〜1013/cm2程度のド
ーズ量で打ち込む等の方法がある。特に、ドーズ量が前
述の値程度であれば、Pチャンネルトランジスタ、Nチ
ャンネルトランジスタ共オフ電流が最小になるように、
Vthを制御することができる。従って、CMOS型のTFT素子
を形成する場合においてもPch,Nchを選択的にチャンネ
ルドープせずに、全面を同一の工程でチャンネルドープ
することもできる。Also, doping the channel region with an impurity, Vt
Means for controlling h (threshold voltage) is also very effective. In a polycrystalline silicon TFT formed by the solid phase growth method, N
Vth of the channel transistor shifts in the depletion direction, and P-channel transistor tends to shaft in the enhancement direction. When the TFT is hydrogenated, the tendency becomes more remarkable. Therefore, if the channel region is doped with an impurity of about 10 15 to 10 19 / cm 3 , the shift of Vth can be suppressed. For example, the first
In the figure, there is a method of implanting an impurity such as B (boron) at a dose of about 10 11 to 10 13 / cm 2 by ion implantation or the like before forming a gate electrode. In particular, when the dose is about the above value, the off-state current of both the P-channel transistor and the N-channel transistor is minimized.
Vth can be controlled. Therefore, even when a CMOS type TFT element is formed, the entire surface can be channel-doped in the same step without selectively channel-doping Pch and Nch.
尚、本発明は、第1図の実施例に示したPoly−SiTFT
に限らず、単結晶シリコン上のゲート絶縁膜、多結晶シ
リコン・微結晶シリコン・非晶質シリコン等の非単結晶
シリコン上のゲート絶縁膜等に用いることもできる。
又、本発明はTFTに限らず、絶縁ゲート型半導体素子全
般に応用できる。更に、本発明の酸化膜はゲート絶縁膜
以外にも、層間絶縁膜・バッシベーション膜等にも用い
ることができ、絶縁耐圧が高い絶縁膜を低温形成できる
という大きなメリットがある。In addition, the present invention relates to a poly-Si TFT shown in the embodiment of FIG.
The present invention is not limited to this, and can be used for a gate insulating film over single crystal silicon, a gate insulating film over non-single-crystal silicon such as polycrystalline silicon, microcrystalline silicon, and amorphous silicon.
Further, the present invention is not limited to TFTs, but can be applied to insulated gate semiconductor devices in general. Further, the oxide film of the present invention can be used not only as a gate insulating film but also as an interlayer insulating film, a passivation film, and the like, and has a great merit that an insulating film having a high withstand voltage can be formed at a low temperature.
[発明の効果] 以上述べたように、本発明によれば絶縁耐圧が高く、
界面準位密度の低い酸化膜を低温で形成することができ
る。特に、多結晶シリコン上に本発明によるスパッタ法
で酸化膜を形成した場合は、多結晶シリコンを熱酸化し
酸化膜を形成した場合よりも、絶縁耐圧を高く、界面準
位密度を低くすることができた。更に、熱酸化膜よりも
TFTの電界効果移動度が大幅に向上するという効果もあ
る。その結果、絶縁性非晶質材料上に高性能な半導体素
子を形成することが可能となり、大型で高解像度の液晶
表示パネルや高速で高解像度の密着型イメージセンサや
三次元IC等を容易に形成できるようになった。又、本発
明による酸化膜の形成方法は低温プロセスであるため、
基板として安価なガラス基板を用いることも可能であ
る。三次元ICにおいては下層部の素子に悪影響(例え
ば、不純物の再分布等)を与えずに上層部の素子を形成
することもできる。[Effects of the Invention] As described above, according to the present invention, the withstand voltage is high,
An oxide film having a low interface state density can be formed at a low temperature. In particular, when an oxide film is formed on polycrystalline silicon by the sputtering method according to the present invention, the withstand voltage is higher and the interface state density is lower than when an oxide film is formed by thermally oxidizing polycrystalline silicon. Was completed. Furthermore, compared to thermal oxide film
Another effect is that the field-effect mobility of the TFT is greatly improved. As a result, it is possible to form a high-performance semiconductor device on an insulating amorphous material, and it is easy to produce a large, high-resolution liquid crystal display panel, a high-speed, high-resolution contact-type image sensor, or a three-dimensional IC. Can be formed. Also, since the method for forming an oxide film according to the present invention is a low-temperature process,
It is also possible to use an inexpensive glass substrate as the substrate. In a three-dimensional IC, an upper-layer element can be formed without adversely affecting the lower-layer element (for example, redistribution of impurities).
また、本発明は、第1図の実施例に示したTFT以外に
も、絶縁ゲート型半導体素子全般に応用できる。Further, the present invention can be applied to general insulated gate semiconductor devices other than the TFT shown in the embodiment of FIG.
第1図(a)〜(e)は本発明の実施例における半導体
装置の製造工程図である。 101……絶縁性非晶質材料 102……シリコン層 103……多結晶シリコン層 104……ゲート絶縁膜 105……ゲート電極 106……ソース・ドレイン領域 107……層間絶縁膜 108……コンタクト穴 109……配線1 (a) to 1 (e) are manufacturing process diagrams of a semiconductor device according to an embodiment of the present invention. 101 insulating amorphous material 102 silicon layer 103 polycrystalline silicon layer 104 gate insulating film 105 gate electrode 106 source / drain region 107 interlayer insulating film 108 contact hole 109 ... Wiring
Claims (4)
方法において、 少なくともアルゴンガスとヘリウムガスを含むガスを槽
内に導入して、スパッタ法によりシリコン酸化膜からな
るゲート絶縁膜を形成することを特徴とする絶縁ゲート
型電界効果トランジスタの製造方法。In a method of manufacturing an insulated gate field effect transistor, a gas containing at least argon gas and helium gas is introduced into a tank, and a gate insulating film made of a silicon oxide film is formed by a sputtering method. Of manufacturing an insulated gate field effect transistor.
ことを特徴とする請求項1記載の絶縁ゲート型電界効果
トランジスタの製造方法。2. The method according to claim 1, wherein the concentration of the helium gas is 5% or more.
0Pa未満で形成されることを特徴とする請求項1又は請
求項2に記載の絶縁ゲート型電界効果トランジスタの製
造方法。3. The gate insulating film has an internal pressure of 1.
3. The method for manufacturing an insulated gate field effect transistor according to claim 1, wherein the method is performed at less than 0 Pa.
チャンネル領域の少なくとも一部が非単結晶半導体であ
ることを特徴とする請求項1乃至請求項3のいずれか一
項に記載の絶縁ゲート型電界効果トランジスタの製造方
法。4. The insulated gate electric field according to claim 1, wherein at least a part of a channel region of the insulated gate field effect transistor is made of a non-single-crystal semiconductor. Method for manufacturing effect transistor.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17232889A JP2811763B2 (en) | 1989-07-04 | 1989-07-04 | Method for manufacturing insulated gate field effect transistor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17232889A JP2811763B2 (en) | 1989-07-04 | 1989-07-04 | Method for manufacturing insulated gate field effect transistor |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0336768A JPH0336768A (en) | 1991-02-18 |
| JP2811763B2 true JP2811763B2 (en) | 1998-10-15 |
Family
ID=15939870
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17232889A Expired - Fee Related JP2811763B2 (en) | 1989-07-04 | 1989-07-04 | Method for manufacturing insulated gate field effect transistor |
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| Country | Link |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3921548A1 (en) * | 1989-06-30 | 1991-01-10 | Waasner Elektrotechnische Fabr | SHEET PACKAGE FROM EDGE STRIP TAPE SHEETS AND METHOD FOR THE PRODUCTION THEREOF |
| JP3637069B2 (en) | 1993-03-12 | 2005-04-06 | 株式会社半導体エネルギー研究所 | Method for manufacturing semiconductor device |
| JP4689079B2 (en) * | 2001-06-01 | 2011-05-25 | 株式会社モリタ | Opening support system, opening support method |
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1989
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