JP2874271B2 - Method for manufacturing semiconductor device - Google Patents
Method for manufacturing semiconductor deviceInfo
- Publication number
- JP2874271B2 JP2874271B2 JP9690990A JP9690990A JP2874271B2 JP 2874271 B2 JP2874271 B2 JP 2874271B2 JP 9690990 A JP9690990 A JP 9690990A JP 9690990 A JP9690990 A JP 9690990A JP 2874271 B2 JP2874271 B2 JP 2874271B2
- Authority
- JP
- Japan
- Prior art keywords
- film
- hydrogen
- temperature
- annealing
- layer
- 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 60
- 239000004065 semiconductor Substances 0.000 title claims description 32
- 238000004519 manufacturing process Methods 0.000 title claims description 15
- 239000001257 hydrogen Substances 0.000 claims description 49
- 229910052739 hydrogen Inorganic materials 0.000 claims description 49
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 47
- 239000013078 crystal Substances 0.000 claims description 30
- 229910021421 monocrystalline silicon Inorganic materials 0.000 claims description 19
- 239000012535 impurity Substances 0.000 claims description 11
- 238000009792 diffusion process Methods 0.000 claims description 10
- 239000010408 film Substances 0.000 description 65
- 238000000137 annealing Methods 0.000 description 46
- 229910021417 amorphous silicon Inorganic materials 0.000 description 38
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 38
- 239000000758 substrate Substances 0.000 description 28
- 239000007790 solid phase Substances 0.000 description 22
- 238000005268 plasma chemical vapour deposition Methods 0.000 description 21
- 238000005984 hydrogenation reaction Methods 0.000 description 20
- 239000007789 gas Substances 0.000 description 19
- 238000010438 heat treatment Methods 0.000 description 19
- 230000007547 defect Effects 0.000 description 17
- 239000010409 thin film Substances 0.000 description 15
- 230000015572 biosynthetic process Effects 0.000 description 11
- 230000000694 effects Effects 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- 230000008569 process Effects 0.000 description 9
- 238000004544 sputter deposition Methods 0.000 description 8
- 229910004298 SiO 2 Inorganic materials 0.000 description 7
- 238000003795 desorption Methods 0.000 description 7
- 230000005669 field effect Effects 0.000 description 6
- 239000011521 glass Substances 0.000 description 6
- 238000005468 ion implantation Methods 0.000 description 6
- 239000004973 liquid crystal related substance Substances 0.000 description 6
- 229910021424 microcrystalline silicon Inorganic materials 0.000 description 6
- 238000009832 plasma treatment Methods 0.000 description 6
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 4
- 229910052804 chromium Inorganic materials 0.000 description 4
- 238000002161 passivation Methods 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- YZCKVEUIGOORGS-UHFFFAOYSA-N Hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 description 3
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 229910052796 boron Inorganic materials 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000000280 densification Methods 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- 239000011810 insulating material Substances 0.000 description 3
- 238000004518 low pressure chemical vapour deposition Methods 0.000 description 3
- 229910052750 molybdenum Inorganic materials 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000010453 quartz Substances 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- 229910052719 titanium Inorganic materials 0.000 description 3
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000005229 chemical vapour deposition Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000010894 electron beam technology Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 238000005224 laser annealing Methods 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000004767 nitrides Chemical class 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 230000007261 regionalization Effects 0.000 description 2
- 230000000630 rising effect Effects 0.000 description 2
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 2
- 238000009751 slip forming Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 229910004261 CaF 2 Inorganic materials 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- 229910017875 a-SiN Inorganic materials 0.000 description 1
- 229910021486 amorphous silicon dioxide Inorganic materials 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229910052594 sapphire Inorganic materials 0.000 description 1
- 239000010980 sapphire Substances 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
Landscapes
- Thin Film Transistor (AREA)
- Recrystallisation Techniques (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関する。The present invention relates to a method for manufacturing a semiconductor device.
[従来の技術] ガラス、石英等の絶縁性非晶質基板や、SiO2、Si3N4
等の絶縁性非晶質層等の絶縁性非晶質材料上に高性能な
半導体素子を形成する試みが成されている。[Prior art] Insulating amorphous substrates such as glass and quartz, SiO 2 , Si 3 N 4
Attempts have been made to form a high-performance semiconductor element on an insulating amorphous material such as an insulating amorphous layer.
近年、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等へのニーズ
が高まるにつれて、上述のような絶縁材料上に形成する
半導体素子の高性能化、大面積化、低コスト化の実現が
必須となっている。In recent years, as the need for large, high-resolution liquid crystal display panels, high-speed, high-resolution contact-type image sensors, three-dimensional ICs, and the like has increased, the performance of semiconductor elements formed on insulating materials as described above has increased, It is essential to increase the area and reduce the cost.
特に、大型の液晶表示パネル等においては、低コスト
の要求を満たすために、安価なガラス基板上に薄膜トラ
ンジスタ(TFT)を形成することが必須の要求になりつ
つある。(Solid State Electronics Vol.32(5)p.39
1(1989)、 IEEE Electron Device Letters Vol.10
(3)p.123(1989)、 IEEE Transactions on Electro
n Devices,Vol.36(3)p.529(1989)) また、TFTの高性能化のためには、a−Si(非晶質シ
リコン)よりもpoly−Si(多結晶シリコン)を用いた方
が有利ではあるが、結晶粒界等にダングリングボンドが
多数存在し、キャリアに対するトラップ準位となりキャ
リアの伝導に対して障壁として働く。(J.Y.W.Seto,J.A
ppl.Phys.,46,p5247(1975))。従って、多結晶シリコ
ン薄膜トランジスタの性能を向上させる為には、前記欠
陥を低減させる必要がある。(J.Appl.Phys.,53(2),
p1193(1982))。この為に水素による前記欠陥の終端
化が行われており、この様な水素化の方法としては、水
素プラズマ処理法、水素イオン注入法、あるいはプラズ
マ窒化膜からの水素の拡散法等が知られている。In particular, in the case of large-sized liquid crystal display panels and the like, forming a thin film transistor (TFT) on an inexpensive glass substrate is becoming an essential requirement in order to satisfy the requirement of low cost. (Solid State Electronics Vol.32 (5) p.39
1 (1989), IEEE Electron Device Letters Vol.10
(3) p.123 (1989), IEEE Transactions on Electro
n Devices, Vol. 36 (3) p. 529 (1989)) To improve the performance of TFTs, poly-Si (polycrystalline silicon) was used rather than a-Si (amorphous silicon). Although it is more advantageous, a large number of dangling bonds are present at the crystal grain boundaries and the like, and serve as trap levels for carriers and act as barriers for carrier conduction. (JYWSeto, JA
ppl.Phys., 46, p5247 (1975)). Therefore, in order to improve the performance of the polycrystalline silicon thin film transistor, it is necessary to reduce the defects. (J. Appl. Phys., 53 (2),
p1193 (1982)). For this reason, the above-mentioned defects are terminated with hydrogen. As such a hydrogenation method, a hydrogen plasma treatment method, a hydrogen ion implantation method, a method of diffusing hydrogen from a plasma nitride film, and the like are known. ing.
[発明が解決しようとする課題] しかし、従来の水素化の方法では、以下に述べる欠点
があった。(1)水素イオン注入法においては、イオン
注入装置と言う高価な装置を必要とし、数百Å程度の多
結晶シリコン層に制御性良く水素を打ち込むことが困難
である等の欠点がある。(2)プラズマ窒化膜からの水
素の拡散法においては、水素の供給が不十分であるため
に、水素プラズマ処理と比べて特性が十分向上しない等
の欠点がある。(3)水素プラズマ処理法においては、
特性の向上という点では優れているが、プラズマダメー
ジによるゲート耐圧不良、閾値電圧(Vth)のシフト等
の不良が多発する等の欠点がある。[Problems to be Solved by the Invention] However, the conventional hydrogenation method has the following disadvantages. (1) The hydrogen ion implantation method has a drawback that an expensive apparatus called an ion implantation apparatus is required, and it is difficult to implant hydrogen into a polycrystalline silicon layer of about several hundreds of square meters with good controllability. (2) In the method of diffusing hydrogen from a plasma nitride film, there is a drawback that characteristics are not sufficiently improved as compared with the hydrogen plasma treatment due to insufficient supply of hydrogen. (3) In the hydrogen plasma processing method,
Although it is excellent in terms of improvement in characteristics, it has disadvantages such as a frequent occurrence of defects such as gate breakdown voltage failure and threshold voltage (Vth) shift due to plasma damage.
そこで、本発明は水素化によるTFT特性向上の効果を
確保しつつ、前述の問題を解決した半導体装置の製造方
法を提供することを目的とする。Therefore, an object of the present invention is to provide a method of manufacturing a semiconductor device which solves the above-mentioned problem while securing the effect of improving TFT characteristics by hydrogenation.
[課題を解決するための手段] 本発明の半導体装置の製造方法は、以下の特徴を有す
る。[Means for Solving the Problems] The method for manufacturing a semiconductor device of the present invention has the following features.
本発明の半導体装置の製造方法は、基板上にゲート電
極と、ゲート絶縁膜と、チャンネル領域となる非単結晶
シリコン層と、ソース・ドレイン領域となる不純物がド
ープされた非単結晶半導体層とをこの順で形成し、前記
非単結晶半導体層上に水素の拡散を防止するキャップ層
を形成して熱処理することにより、前記非単結晶半導体
層から脱離した水素によって前記非単結晶シリコン層の
水素化を行うことを特徴とする。The method for manufacturing a semiconductor device according to the present invention includes the steps of: forming a gate electrode, a gate insulating film, a non-single-crystal silicon layer serving as a channel region, and a non-single-crystal semiconductor layer doped with impurities serving as source / drain regions on a substrate. Are formed in this order, and a heat treatment is performed by forming a cap layer on the non-single-crystal semiconductor layer to prevent diffusion of hydrogen, so that the non-single-crystal silicon layer is formed by hydrogen released from the non-single-crystal semiconductor layer. Is characterized by performing hydrogenation.
[実施例] 以下、第1図をもとに本発明の実施例を説明する。第
1図は本発明に基づく半導体装置の製造工程図である。Embodiment An embodiment of the present invention will be described below with reference to FIG. FIG. 1 is a manufacturing process diagram of a semiconductor device according to the present invention.
第1図(a)は、ガラス、石英等の絶縁性非晶質基
板、若しくはSiO2、Si3N4等の絶縁性非晶質材料層、若
しくはサファイア基板(Al2O3)あるいはMgO・Al2O3,B
P,CaF2等の絶縁性結晶基板等の絶縁材料101上にゲート
電極102を形成する工程である。具体的には、(1)プ
ラズマCVD法、ECR−PCVD法、スパッタ法、多結晶Si薄膜
中へのSiイオンインプランテーション法等の手段によっ
て、ボロン等の不純物をドープしたa−Si層を約3000〜
7000Å形成し、固相成長法やレーザーアニール法等で多
結晶化する方法、(2)スパッタ法等でMo、Cr、Ta等の
高融点金属を形成する方法等がある。本実施例では、プ
ラズマCVD法で形成したa−Si層を固相成長法で多結晶
化する場合を例に取って説明する。プラズマCVD法の成
膜ガスはSiH4、H2ガスを用い、ドーピングガスにはB2H6
ガスを用いた。基板温度は150〜250℃、内圧は0.8Torr
で、13.56MHzのrf電源を用いた。B2H6、SiH4の流量比は
[B2H6]/[SiH4]=3×10-3〜5×10-2程度となるよ
うに設定した。尚、成膜されたa−Si層中に含まれるボ
ロン濃度は上述のガス混合比とほぼ対応している。続い
て、a−Si層を固相成長させ、ゲート電極102の形にパ
ターン形成する。尚、固相成長はパターン形成後に行っ
てもよい。続いて、固相成長のアニール条件に関して述
べる。まず、450℃で30min.N2雰囲気中でプリアニール
してa−Si層中に含まれる水素を脱離させる。これは、
水素がa−Si中に含まれたまま固相成長アニールを行う
と、水素が抜けた部分が空孔となり、多孔質の膜になっ
てしまうのを防ぐ目的とする。尚、プラズマCVD法を用
いる場合、成膜ガスにHeガスを用いて希釈を行うと、a
−Si層中に取り込まれる水素量を減らすことができると
いう利点があるので更に望ましい。この後、固相成長ア
ニール工程に移る。アニール条件はN2ガス中、550〜650
℃の温度で4〜72時間程度である。この固相成長アニー
ルによって、a−Si層は多結晶化し、ゲート電極中のSi
グレイン平均粒径は約1〜3μmまでになり、5μm以
上の粒径をしめすグレインも多数現れる。アニールはN2
アニールに限ることはなく、レーザービームアニール、
ハロゲンランプアニール等でもよい。このアニール工程
時にはa−Si層成膜時に混入させたボロン原子も同時に
活性化される。この結果、多結晶シリコンゲート電極
(p+poly−Si)106の抵抗率は、1〜3×10-3Ω・cm
となり、通常のLPCVDで成膜した平均粒径3000Å以下で
粒径1μm以上の結晶粒を全く含まない多結晶Siを用い
たn型ドープトゲート電極の抵抗率 2.5×10-3Ω・cm
と、ほぼ同程度の低効率が得られる。尚、ゲート電極の
固成長アニールは、第1図(c)に示す工程で行うチャ
ンネル領域とソースドレイン領域の固相成長アニール工
程で行うことも可能である。即ち、ゲート電極のパター
ン形成までを行い、工程(c)で固相成長させることも
可能であり、工程の短縮になる。FIG. 1A shows an insulating amorphous substrate such as glass or quartz, an insulating amorphous material layer such as SiO 2 or Si 3 N 4 , or a sapphire substrate (Al 2 O 3 ) or MgO. Al 2 O 3 , B
This is a step of forming a gate electrode 102 on an insulating material 101 such as an insulating crystal substrate such as P or CaF 2 . Specifically, (1) the a-Si layer doped with impurities such as boron is removed by a method such as a plasma CVD method, an ECR-PCVD method, a sputtering method, or a Si ion implantation method into a polycrystalline Si thin film. 3000 ~
There is a method of forming 7000 ° and polycrystallizing by a solid phase growth method or a laser annealing method, and (2) a method of forming a high melting point metal such as Mo, Cr, and Ta by a sputtering method or the like. In this embodiment, a case where an a-Si layer formed by a plasma CVD method is polycrystallized by a solid phase growth method will be described as an example. The plasma CVD method uses SiH 4 and H 2 gases as the deposition gas, and B 2 H 6 as the doping gas.
Gas was used. Substrate temperature is 150 ~ 250 ℃, internal pressure is 0.8Torr
A 13.56 MHz rf power source was used. The flow ratio of B 2 H 6 and SiH 4 was set so that [B 2 H 6 ] / [SiH 4 ] = about 3 × 10 −3 to 5 × 10 −2 . The concentration of boron contained in the formed a-Si layer substantially corresponds to the above-mentioned gas mixture ratio. Subsequently, the a-Si layer is solid-phase grown and patterned in the shape of the gate electrode 102. The solid phase growth may be performed after the pattern formation. Next, the annealing conditions for solid phase growth will be described. First, hydrogen contained in the a-Si layer is desorbed by pre-annealing at 450 ° C. in a 30 min. N 2 atmosphere. this is,
When the solid phase growth annealing is performed while hydrogen is contained in a-Si, the portion from which hydrogen has escaped becomes a hole, and the purpose is to prevent a porous film from being formed. In the case of using the plasma CVD method, if dilution is performed using He gas as a film forming gas, a
-It is more desirable because there is an advantage that the amount of hydrogen taken into the Si layer can be reduced. Thereafter, the process proceeds to a solid phase growth annealing step. 2 gas annealing conditions are N, 550 to 650
It is about 4 to 72 hours at a temperature of ° C. By this solid phase growth annealing, the a-Si layer is polycrystallized and the Si in the gate electrode is
The average grain size is up to about 1 to 3 μm, and many grains having a grain size of 5 μm or more appear. Annealing is N 2
Not limited to annealing, laser beam annealing,
Halogen lamp annealing may be used. At the time of this annealing step, boron atoms mixed during the formation of the a-Si layer are also activated at the same time. As a result, the resistivity of the polycrystalline silicon gate electrode (p + poly-Si) 106 is 1-3 × 10 −3 Ω · cm.
The resistivity of an n-type doped gate electrode using polycrystalline Si formed by ordinary LPCVD and having an average particle diameter of 3000 ° or less and containing no crystal grains having a particle diameter of 1 μm or more is 2.5 × 10 −3 Ω · cm.
, Almost the same efficiency can be obtained. The solid growth annealing of the gate electrode can be performed in a solid phase growth annealing step of the channel region and the source / drain region performed in the step shown in FIG. That is, it is also possible to perform the process up to the pattern formation of the gate electrode and to perform the solid phase growth in the step (c), thereby shortening the process.
第1図(b)は、プラズマCVD法またはECR−PCVD法ま
たはCVD法またはスパッタ法等により、ゲート絶縁膜103
を成すSiO2層を約300Å〜2000Å程度形成する工程であ
る。尚、ゲート電極に多結晶シリコンを用いた場合は、
該多結晶シリコンを熱酸化法によって酸化し、SiO2層を
形成する方法もある。又、ゲート絶縁膜としては、SiO2
以外にもSi1-xOx(0<x<1)、Si1-xNx(0<x<
1)、Si1-x-yOxNy(0<x<1,0<y<1)等の絶縁膜
を用いてもよい。Si1-xNx(0<x<1)をプラズマCVD
法で形成する場合を例にとると、成膜ガスとしては、Si
H4、NH3、N2を用い、基板温度を300℃〜400℃程度に保
ち、rfパワーを印加し上記ガスを分解することでSi1-xN
x(0<x<1)層を形成することができる。FIG. 1B shows a gate insulating film 103 formed by a plasma CVD method, an ECR-PCVD method, a CVD method, a sputtering method, or the like.
This is a step of forming a SiO 2 layer of about 300 to 2000 °. When polycrystalline silicon is used for the gate electrode,
There is also a method of oxidizing the polycrystalline silicon by a thermal oxidation method to form an SiO 2 layer. Also, as the gate insulating film, SiO 2
In addition, Si 1-x O x (0 <x <1), Si 1-x N x (0 <x <
1), an insulating film such as Si 1-xy O x Ny (0 <x <1, 0 <y <1) may be used. Plasma CVD of Si 1-x N x (0 <x <1)
In the case of forming by the method, for example, Si is used as a film forming gas.
H 4, NH 3, using N 2, keeping the substrate temperature at about 300 ° C. to 400 ° C., by decomposing the gas to apply the rf power Si 1-x N
x (0 <x <1) layers can be formed.
第1図(c)は、該ゲート絶縁膜103上にチャンネル
領域を成す非晶質シリコンまたは微結晶シリコンまたは
多結晶シリコン等の非単結晶シリコン層104を100Å〜20
00Å程度形成し、熱処理等によって該非単結晶シリコン
層を結晶成長させ多結晶化する工程である。FIG. 1C shows that a non-single-crystal silicon layer 104 such as amorphous silicon, microcrystalline silicon, or polycrystalline silicon forming a channel region is
In this step, the non-single-crystal silicon layer is crystal-grown by heat treatment or the like to form a polycrystal.
該非単結晶シリコン層の形成方法としては以下に述べ
るような方法がある。As a method for forming the non-single-crystal silicon layer, there is a method described below.
(1)減圧CVD法で580℃〜650℃程度で多結晶シリコン
薄膜を堆積させる。(1) A polycrystalline silicon thin film is deposited at about 580 ° C. to 650 ° C. by a low pressure CVD method.
(2)EB(Electron Beam)蒸着法、スパッタ法、プラ
ズマCVD法等で非晶質シリコン薄膜を堆積後、550℃〜65
0℃程度で2〜70時間程度、固相成長アニール(レーザ
ーアニール法等で短時間で多結晶化する方法もある)を
行い、粒径1〜2μm以上の大粒径の多結晶シリコン薄
膜を形成する。(2) After depositing an amorphous silicon thin film by EB (Electron Beam) evaporation method, sputtering method, plasma CVD method, etc.
A solid phase growth anneal (some methods such as a laser anneal method to polycrystallize in a short time) is performed at about 0 ° C. for about 2 to 70 hours to form a polycrystalline silicon thin film having a large grain size of 1 to 2 μm or more. Form.
(3)減圧CVD法等で多結晶シリコン薄膜を堆積後、イ
オンインプラ法により、Si等を打ち込み、該多結晶シリ
コン薄膜を非晶質化した後、550℃〜650℃程度で固相成
長アニール(レーザーアニール法等で短時間で多結晶化
する方法もある)を行い、粒径1〜2μm程度の大粒径
多結晶シリコン薄膜を形成する。(3) After depositing a polycrystalline silicon thin film by a low-pressure CVD method or the like, implanting Si or the like by an ion implantation method to amorphize the polycrystalline silicon thin film, and then perform solid phase growth annealing at about 550 ° C. to 650 ° C. (There is also a method of polycrystallizing in a short time by a laser annealing method or the like) to form a large-diameter polycrystalline silicon thin film having a particle diameter of about 1 to 2 μm.
尚、上述の方法で多結晶シリコンを形成した場合、結
晶化度が100%に近い、文字通りの多結晶シリコンとな
る場合と、結晶化度が50%程度〜90%程度の多結晶シリ
コンとなる場合がある。この場合、後者は多結晶シリコ
ンと呼ぶよりも微結晶シリコンと呼ぶ方がふさわしいか
も知れないが、本特許では、特に断わりが無い場合は、
両者を含めて多結晶シリコンと呼ぶことにする。また、
非単結晶性のシリコン薄膜としては、上述の多結晶シリ
コン薄膜以外にも、微結晶シリコンや非晶質シリコン薄
膜を用いてもよい。Note that when polycrystalline silicon is formed by the above-described method, the crystallinity is close to 100%, literally polycrystalline silicon, and the polycrystalline silicon has a crystallinity of about 50% to about 90%. There are cases. In this case, the latter may be more appropriate to be called microcrystalline silicon than polycrystalline silicon, but in this patent, unless otherwise specified,
Both of them will be referred to as polycrystalline silicon. Also,
As the non-single-crystal silicon thin film, microcrystalline silicon or amorphous silicon thin film may be used in addition to the above-described polycrystalline silicon thin film.
成膜条件の一例を、以下に述べる。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。尚、ゲート絶縁膜をプラズマCV
D法で形成した場合は、a−SiTFTの製造工程と全く同様
にゲート絶縁膜と非晶室シリコン層を真空を破らずに連
続形成することができ、ゲート絶縁膜とシリコン層の界
面準位の低減や再現性の向上等の効果がある。An example of the film forming conditions is described below. The substrate temperature is maintained at about room temperature to about 600 ° C. by plasma CVD, and monosilane or a gas obtained by diluting monosilane with hydrogen, argon, helium, or the like is introduced into the reaction chamber, and high-frequency energy is applied to decompose the gas to obtain a desired substrate. A silicon layer on top is 100 mm thick
Formed about 2000 mm. In addition, the gate insulating film is plasma CV
In the case of forming by the D method, the gate insulating film and the amorphous silicon layer can be continuously formed without breaking the vacuum in exactly the same manner as in the manufacturing process of the a-Si TFT, and the interface state between the gate insulating film and the silicon layer can be formed. This has the effect of reducing the noise and improving the reproducibility.
続いて、該非単結晶シリコン層104を熱処理等により
結晶成長させ多結晶化する。熱処理条件は、非単結晶シ
リコン層の成膜方法によってその最適条件が異なる。プ
ラズマCVD法で成膜した場合を例にとると、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。Subsequently, the non-single-crystal silicon layer 104 is polycrystallized by crystal growth by heat treatment or the like. The optimum conditions for the heat treatment differ depending on the method of forming the non-single-crystal silicon layer. Taking a case where the film is formed by the plasma CVD method as an example, there are the following differences depending on the substrate temperature during the film formation.
(1)プラズマCVD法で基板温度が室温〜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法
で成膜後、真空を破る前に非晶質シリコン膜をアニール
する。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
無され、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このアニ
ールを省くこともできる。(1) A film formed by plasma CVD 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 is formed at about 200 to 300 ° C. Hydrogen in the film can be removed by a heat treatment at a lower temperature than that of the formed film. An example of the heat treatment condition is described below. After the film is formed by the plasma CVD method, the amorphous silicon film is annealed before breaking the vacuum. 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 a proper heat treatment is performed, the film is not densified, and the incorporation of oxygen and the like is prevented. The heat treatment temperature is
300 ° C. or higher is desirable, 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,
When annealing is performed continuously without breaking the vacuum, the annealing can be omitted.
続いて、熱処理等によって前記非晶質シリコン膜を固
相成長させる。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程度以上のの大粒径の結晶粒を
含む多結晶シリコンが形成される。尚、前記緻密化のた
めのアニール及び固相成長時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。Subsequently, the amorphous silicon film is solid-phase grown by heat treatment or the like. 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 containing crystal grains having a large grain size of about 2 μm or more is formed. In addition, it is not preferable that both the annealing for densification and the annealing during solid phase growth 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 is increased (especially when the temperature exceeds 300 ° C.), hydrogen in the film is desorbed, and when the rate of temperature rise is rapid, defects are easily formed in the film. In some cases, pinholes are formed or the film is peeled off. 20 at least at temperatures above 300 ° C
When the temperature is gradually increased at a temperature rising rate lower than 5 ° C./min (a temperature rising rate lower than 5 ° C./min is particularly desirable), the number of defects in the film decreases.
(2)プラズマCVD法で基板温度が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、上述の緻密化
のためのアーニルを省くこともできる。固相成長条件
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1〜2
μm程度の大粒径の結晶粒を含む多結晶シリコンが形成
される。尚、550℃〜650℃までの昇温方法は、(1)の
場合と同様に少なくとも300℃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。
尚、基板温度は、150℃〜200℃の間が、結晶粒径が比較
的大きく、固相成長時に所定の固相成長温度まで昇温す
る際発生する膜の剥離等も起こり難く、特に好ましい。(2) A film formed at a substrate temperature of about 150 ° C. to 300 ° C. by a plasma CVD method has a smaller amount of hydrogen in the film but has a smaller amount of hydrogen than an amorphous silicon film formed at a low temperature. The release temperature shifts to higher temperatures. However, since the film after film formation is denser than a film formed at a low temperature, arnyl for the above-described densification can be omitted. Solid phase growth conditions are as follows: When heat treatment at about 550 ° C. to 650 ° C. is performed for several hours to about 40 hours, desorption of hydrogen and crystal growth occur, and the crystal grain size is 1 to 2 hours.
Polycrystalline silicon containing crystal grains having a large grain size of about μm is formed. The method of raising the temperature from 550 ° C. to 650 ° C. is similar to the case of (1), in that at least at a temperature of 300 ° C. or more, the temperature is raised at a rate of 20 ° C./min (preferably 5 ° C./min). Is desirably gradually increased to reduce defects in the film.
The substrate temperature is preferably between 150 ° C. and 200 ° C., the crystal grain size is relatively large, and it is difficult to cause peeling of the film that occurs when the temperature is raised to a predetermined solid phase growth temperature during solid phase growth, which is particularly preferable. .
(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場合がある。(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 may be important.
第1図(d)は、ソースドレイン領域を成す不純物を
ドープした非単結晶半導体層105を形成し、該非単結晶
半導体層上に水素の拡散を防止するキャップ層106を形
成し、300℃〜600℃程度でアニールを行い該非単結晶層
を多結晶化すると同時に、該非単結晶層から脱離した水
素によって、チャンネル領域の非単結晶シリコン層を水
素化する工程である。FIG. 1D shows a case where a non-single-crystal semiconductor layer 105 doped with impurities forming a source / drain region is formed, and a cap layer 106 for preventing diffusion of hydrogen is formed on the non-single-crystal semiconductor layer. This is a step of annealing at about 600 ° C. to polycrystallize the non-single-crystal layer and hydrogenate the non-single-crystal silicon layer in the channel region with hydrogen released from the non-single-crystal layer.
nチャンネルTFTの場合はn型半導体層を、pチャン
ネルTFTの場合はp型半導体層を形成する。本実施例で
は、プラズマCVD法で形成した不純物をドープしたa−S
i層を固相成長法で多結晶化する場合を例に取って説明
する。プラズマCVD法の成膜ガスはSiH4、H2ガスを用
い、ドーピングガスにはB2H6ガス(pチャンネル)若し
くはPH3ガス(nチャンネル)を用いた。基板温度は150
〜250℃、内圧は0.8Torrで、13.56MHzのrf電源を用い
た。B2H6、PH3とSiH4の流量比は[B2H6]/[SiH4]=
3×10-3〜5×10-2、[PH3]/[SiH4]=3×10-3〜
5×10-2程度となるように設定した。尚、成膜されたa
−Si層中に含まれる不純物濃度は上述のガス混合比とほ
ぼ対応している。また、非晶質シリコン薄膜中には10%
程度の水素が含まれている。In the case of an n-channel TFT, an n-type semiconductor layer is formed, and in the case of a p-channel TFT, a p-type semiconductor layer is formed. In this embodiment, a-S doped with an impurity formed by a plasma CVD method is used.
The case where the i-layer is polycrystallized by the solid phase growth method will be described as an example. As a film forming gas of the plasma CVD method, SiH 4 and H 2 gases were used, and as a doping gas, a B 2 H 6 gas (p channel) or a PH 3 gas (n channel) was used. Substrate temperature is 150
250250 ° C., the internal pressure was 0.8 Torr, and a 13.56 MHz rf power source was used. The flow ratio of B 2 H 6 , PH 3 and SiH 4 is [B 2 H 6 ] / [SiH 4 ] =
3 × 10 −3 to 5 × 10 −2 , [PH 3 ] / [SiH 4 ] = 3 × 10 −3 to
It was set to be about 5 × 10 -2 . In addition, the formed a
-The concentration of impurities contained in the Si layer substantially corresponds to the gas mixture ratio described above. 10% in amorphous silicon thin film
Contains about hydrogen.
続いて、該非単結晶半導体層105上にキャップ層106を
形成し、300℃〜650℃程度の温度で水素化と多結晶化の
ためのアニールを施す。アニール時間は1時間〜20時間
程度である。このアニールの目的は、該非単結晶半導体
層を熱処理により結晶成長させ、多結晶化すると同時
に、膜中に含まれる水素を脱離、拡散させ、チャンネル
領域を成す多結晶シリコンを水素化することにある。こ
のアニールによって、不純物をドープしたa−Si:Hから
原子状の水素が脱離、拡散し、チャンネル領域を成す多
結晶シリコンの結晶粒界やゲート絶縁膜との界面に存在
するダングリングボンドを終端化する。尚、キャップ層
106としては、a−Si:Hから発生する水素が拡散しにく
い材料が望ましい。例えば、(1)Ti、Cr、Mo、Al等の
金属薄膜をスパッタ法、蒸着法等で300Å〜1μm程度
形成する方法、(2)非晶質窒素珪素(a−SiNx)を10
00Å〜1μm程度形成する方法等がある。特に、Ti、C
r、Mo等をキャップ層に用いた場合は、水素化アニール
の後、キャップ層を全面剥離する必要がなく、ソースド
レイン領域上にそのまま残し、Al等で形成されるソース
ドレイン電極とソースドレイン領域の良好なコンタクト
を確保するためのバッファ層として、そのまま用いるこ
とができる。尚、キャップ層の材質は上記材料に限らず
非晶質二酸化珪素(SiO2)よりも水素が拡散しにくい
(拡散係数が小さい)材料が好ましい。Subsequently, a cap layer 106 is formed on the non-single-crystal semiconductor layer 105, and annealing for hydrogenation and polycrystallization is performed at a temperature of about 300 ° C. to 650 ° C. The annealing time is about 1 hour to 20 hours. The purpose of this annealing is to crystallize the non-single-crystal semiconductor layer by heat treatment and polycrystallize it, and at the same time, desorb and diffuse hydrogen contained in the film to hydrogenate the polycrystalline silicon forming the channel region. is there. By this annealing, atomic hydrogen is desorbed and diffused from the impurity-doped a-Si: H to form dangling bonds existing at the crystal grain boundaries of the polycrystalline silicon forming the channel region and at the interface with the gate insulating film. Terminate. In addition, cap layer
As 106, a material that hardly diffuses hydrogen generated from a-Si: H is desirable. For example, (1) a method of forming a metal thin film of Ti, Cr, Mo, Al or the like to a thickness of about 300 to 1 μm by a sputtering method, a vapor deposition method, or the like; (2) amorphous silicon nitride (a-SiN x )
For example, there is a method of forming about 00Å to about 1 μm. In particular, Ti, C
When r, Mo, or the like is used for the cap layer, there is no need to remove the cap layer entirely after the hydrogenation annealing, and leave the cap layer on the source / drain region, and form a source / drain electrode and a source / drain region formed of Al or the like. Can be used as it is as a buffer layer for ensuring good contact. The material of the cap layer is not limited to the above-mentioned material, but is preferably a material in which hydrogen is less likely to diffuse (has a smaller diffusion coefficient) than amorphous silicon dioxide (SiO 2 ).
続いて、水素化及び多結晶化のためのアニール条件に
関して述べる。まず、所定のアニール温度までの昇温方
法について述べる。本発明では、非晶質シリコン上に水
素拡散防止用のキャップ層を形成してあるため、アニー
ルの方法を最適化しないと、水素の急激な脱離に伴う非
晶質シリコン層の剥離やピンホール等の欠陥発生等の問
題を生ずる。そこで、水素化アニールの条件、特に、所
定の水素化アニール温度までの昇温方法は重要である。
所定の温度に保たれたアニール炉に試料を挿入し、所定
の水素化アニール温度まで所定の昇温速度で昇温して、
所定の水素化温度でアニールする場合、昇温速度は、5
℃/分より遅い方が水素の脱離に伴う欠陥の発生や膜の
剥離が抑制され望ましい。尚、昇温速度は常に一定であ
る必要はなく、上述の値の範囲で変動しても無論構わな
い。尚、アニール温度は300℃〜650℃の間に最適値が存
在する。多結晶化のためには、550℃〜650℃程度の高温
のアニールが必要であるが、450℃程度以上のアニール
温度では、非晶質シリコンからの水素の脱離と脱離した
水素の拡散は効率的に起こるが、多結晶シリコンのダン
グリングボンドへの水素付加の効率が低下する(水素の
付加と脱離が同時に起こるようになるため)。そこで、
一旦550℃〜650℃程度の温度まで昇温し、20分〜1時間
程度アニールを行い、多結晶化と水素の脱離と拡散を促
進した後、400℃程度以下まで冷却し、多結晶シリコン
のダングリングボンド等の欠陥への水素の付加を促進す
るアニールを30分〜2時間程度行うアニール方法はきわ
めて有効である。Subsequently, annealing conditions for hydrogenation and polycrystallization will be described. First, a method for raising the temperature to a predetermined annealing temperature will be described. In the present invention, since a cap layer for preventing hydrogen diffusion is formed on amorphous silicon, if the annealing method is not optimized, peeling of the amorphous silicon layer due to rapid desorption of hydrogen and Problems such as generation of defects such as holes occur. Therefore, conditions for the hydrogenation annealing, particularly, a method of raising the temperature to a predetermined hydrogenation annealing temperature are important.
The sample is inserted into an annealing furnace maintained at a predetermined temperature, and heated to a predetermined hydrogenation annealing temperature at a predetermined heating rate,
When annealing at a predetermined hydrogenation temperature, the heating rate is 5
It is desirable that the temperature be lower than ° C./min because the generation of defects and the peeling of the film due to the desorption of hydrogen are suppressed. It is to be noted that the heating rate does not need to be always constant, and may be changed within the above range. The annealing temperature has an optimum value between 300 ° C and 650 ° C. For polycrystallization, high-temperature annealing at about 550 ° C to 650 ° C is necessary, but at annealing temperatures above 450 ° C, desorption of hydrogen from amorphous silicon and diffusion of desorbed hydrogen Occurs efficiently, but the efficiency of hydrogen addition to dangling bonds in polycrystalline silicon decreases (because hydrogen addition and desorption occur simultaneously). Therefore,
Once the temperature is raised to about 550 ° C to 650 ° C, annealing is performed for about 20 minutes to 1 hour to promote polycrystallization and desorption and diffusion of hydrogen. An annealing method of performing annealing for promoting the addition of hydrogen to defects such as dangling bonds for about 30 minutes to 2 hours is extremely effective.
尚、不純物をドープした非単結晶シリコン層として、
非晶質シリコンでなく微結晶シリコンをプラズマCVD法
等で形成する方法も有効である。微結晶シリコンをプラ
ズマCVDで形成する場合は基板温度を350℃〜400℃程度
と高めにし、SiH4/H2流量比を低めにして、rfパワーを
高めにすることで、容易に形成できる。該半導体層に微
結晶シリコンを用いた場合は、多結晶化しなくても、十
分抵抗率が低いため、上述のアニールの際、550℃〜650
℃程度の高温のアニールを省くことも可能となる。従っ
て、300℃〜450℃程度のアニールを30分〜2時間程度行
うだけで、十分な水素化が成される。As a non-single-crystal silicon layer doped with impurities,
A method of forming microcrystalline silicon instead of amorphous silicon by a plasma CVD method or the like is also effective. When microcrystalline silicon is formed by plasma CVD, it can be easily formed by increasing the substrate temperature to about 350 ° C. to 400 ° C., lowering the SiH 4 / H 2 flow rate ratio, and increasing the rf power. In the case where microcrystalline silicon is used for the semiconductor layer, even if it is not polycrystallized, the resistivity is sufficiently low.
It is also possible to omit annealing at a high temperature of about ° C. Therefore, sufficient hydrogenation can be achieved only by performing annealing at about 300 ° C. to 450 ° C. for about 30 minutes to 2 hours.
第1図(e)は、チャンネル領域を成す非単結晶シリ
コン層104及びソースドレイン領域を成す非単結晶シリ
コン層105及びTi、Mo、Cr等で形成されたキャップ層106
を所定のパターンにエッチングし、続いて、配線材の導
電膜(Al、Cr、ITO等)を1000Å〜1μm程度スパッタ
法等で成膜し、ソース電極110、ドレイン電極109を形成
し、該キャップ層106及び該非単結晶層105をパターン形
成し、ソース領域108及びドレイン領域107を形成する工
程である。FIG. 1 (e) shows a non-single-crystal silicon layer 104 forming a channel region, a non-single-crystal silicon layer 105 forming a source / drain region, and a cap layer 106 formed of Ti, Mo, Cr or the like.
Is etched into a predetermined pattern. Subsequently, a conductive film (Al, Cr, ITO, etc.) of a wiring material is formed to a thickness of about 1000 to 1 μm by a sputtering method or the like, and a source electrode 110 and a drain electrode 109 are formed. This is a step of patterning the layer 106 and the non-single-crystal layer 105 to form the source region 108 and the drain region 107.
第1図(f)は、CVD法、プラズマCVD法、スパッタ法
等により、パッシベーション層111を成膜する工程であ
る。パッシベーション層には窒化シリコン膜のほか酸化
シリコン膜等でもよい。又、シリケイト等の無機系SOG
(スピンオングラス)、シリコーン等の有機系SOGを用
いてもよい。特に、シリコーン等の有機系SOGは塗布後
の熱処理による応力の発生が小さく、大面積に渡りクラ
ック等の欠陥の無い良質のパッシベーション層を形成で
きる。FIG. 1F shows a step of forming the passivation layer 111 by a CVD method, a plasma CVD method, a sputtering method, or the like. The passivation layer may be a silicon oxide film or the like in addition to the silicon nitride film. In addition, inorganic SOG such as silicate
(Spin-on-glass) or organic SOG such as silicone may be used. In particular, an organic SOG such as silicone generates a small amount of stress due to heat treatment after coating, and can form a high-quality passivation layer having no defects such as cracks over a large area.
第1図に示した製造方法で形成したpoly−SiTFTの電
界効果移動度は80〜100cm2/V・s(Nチャンネル)、30
〜40cm2/V・s(Pチャンネル)であり、優れた特性のT
FTをガラス基板上に低温形成することができた。The field-effect mobility of the poly-Si TFT formed by the manufacturing method shown in FIG. 1 is 80 to 100 cm 2 / V · s (N channel),
~ 40cm 2 / V · s (P channel)
FT could be formed on a glass substrate at low temperature.
続いて水素化に伴う閾値電圧制御の問題に関して述べ
る。多結晶シリコンTFTを水素化すると、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
フトするが、チャンネル領域に1015〜1019/cm3程度の不
純物をドープすることで、Vthを制御することができ
る。例えば、第1図において、(1)イオンインプラ法
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。Next, the problem of threshold voltage control accompanying hydrogenation will be described. When polycrystalline silicon TFT is hydrogenated, Nth transistor shifts Vth in depletion direction,
Although the P-channel transistor shifts in the enhancement direction, Vth can be controlled by doping the channel region with an impurity of about 10 15 to 10 19 / cm 3 . For example, in FIG. 1, (1) a method of implanting impurities such as B (boron) at a dose of about 10 11 to 10 13 / cm 2 by ion implantation or the like.
(2)チャンネル領域を成す非単結晶シリコン層成膜時
に、1015〜1019/cm3程度の不純物をドープする方法。
(プラズマCVD法で成膜する場合を例にとると、成膜ガ
スとしてSiH4、H2、B2H6等を用いることで容易に形成で
きる)等がある。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。また、前述の様に、ゲート電極として、従来の熱
拡散法によるN+poly−Siを用いる代わりに、固相成長法
等で形成したP+poly−Siを用いることで、チャンネルド
ープを行わずに、Vthを制御することもできる。(2) A method of doping an impurity of about 10 15 to 10 19 / cm 3 when forming a non-single-crystal silicon layer forming a channel region.
(Taking a case where a film is formed by a plasma CVD method as an example, the film can be easily formed by using SiH4, H2, B2H6, or the like as a film forming gas). In particular, when the dose is about the above-described value, Vth can be controlled such that the off-state current of both the P-channel transistor and the N-channel transistor is minimized. 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. Also, as described above, instead of using N + poly-Si by a conventional thermal diffusion method as a gate electrode, by using P + poly-Si formed by a solid phase growth method or the like, channel doping is not performed. Alternatively, Vth can be controlled.
次に、従来の水素プラズマ処理で多発したプラズマ損
傷による不良が、本発明の水素化では、全く発生しない
理由に関して述べる。Next, the reason why the failure due to the plasma damage frequently generated in the conventional hydrogen plasma processing does not occur at all in the hydrogenation of the present invention will be described.
水素プラズマ処理で発生するダメージの原因は、今の
ところ明らかではないが、プラズマ雰囲気中に浸された
ことにより、チャージアップが起こり、ゲート膜に電圧
が加わった状態になる。更に、基板温度が300℃程度と
比較的高いため、一種のBT(Bias−Temperature)スト
レスが加わり、水素プラズマ時間も1〜2時間程度と長
いために、TFTの不良が生じたとするモデルが現象をよ
く説明する。Although the cause of the damage generated by the hydrogen plasma treatment is not clear at present, charge-up occurs due to immersion in a plasma atmosphere, and a voltage is applied to the gate film. In addition, a relatively high substrate temperature of about 300 ° C. applies a kind of BT (Bias-Temperature) stress, and the hydrogen plasma time is as long as about 1 to 2 hours. Is explained well.
一方、本発明の水素化の方法では、非晶質シリコンを
プラズマCVD法で形成し、アニールによって非晶質シリ
コンから脱離した水素原子によって水素化を行ってい
る。従って、非晶質シリコン成膜時に上述のようなBTス
トレスが加わらなければ、ダメージが発生しなくなる。
実際、非晶質シリコンをプラズマCVD法で成膜しただけ
では、上述のようなBTストレスは殆ど加わらず、本発明
で形成したTFTでは、ダメージによる不良を皆無にする
ことができた。その理由としては、以下の2点が考えら
れる。On the other hand, in the hydrogenation method of the present invention, amorphous silicon is formed by a plasma CVD method, and hydrogenation is performed using hydrogen atoms released from the amorphous silicon by annealing. Therefore, if the BT stress as described above is not applied during the formation of the amorphous silicon, no damage occurs.
Actually, the BT stress as described above was hardly applied only by forming the amorphous silicon film by the plasma CVD method, and the TFT formed by the present invention was able to eliminate defects caused by damage. The following two points can be considered as the reason.
(1)水素プラズマ処理と非晶質シリコンの成膜では、
高周波のパワーが1桁程度違うため(20cm径の電極サイ
ズで水素プラズマ処理:100〜200W、非晶質シリコンの成
膜:10〜20W)、水素プラズマ処理程チャージアップが起
こりにくい。(1) In hydrogen plasma treatment and amorphous silicon film formation,
Since the high-frequency power is different by about one digit (hydrogen plasma processing with electrode size of 20 cm diameter: 100 to 200 W, amorphous silicon film formation: 10 to 20 W), charge-up is less likely to occur as compared with hydrogen plasma processing.
(2)水素プラズマ処理では、水素ガスを分解し原子状
水素を供給しながら、熱拡散によって水素原子を多結晶
シリコン層まで拡散させる必要がある。従って、基板温
度を250℃〜350℃程度の高温に保たなければ、水素化の
効果が激減する。一方、本発明では、原子状水素の供給
とその熱拡散による水素化を、非晶質シリコン成膜時に
行うのではなく、それとは別のアニール工程で行うた
め、非晶質シリコン成膜時の基板温度を低温化すること
が出来る。また、基板温度を低温化(例えば200℃以
下)したほうが、低温で水素が脱離しやすいため、本発
明では非晶質シリコンの成膜温度を低温化したほうが望
ましい。従って、本発明ではBTストレスはより軽減され
る。(2) In the hydrogen plasma treatment, it is necessary to diffuse hydrogen atoms to the polycrystalline silicon layer by thermal diffusion while decomposing hydrogen gas and supplying atomic hydrogen. Therefore, unless the substrate temperature is maintained at a high temperature of about 250 ° C. to 350 ° C., the effect of hydrogenation is drastically reduced. On the other hand, in the present invention, the supply of atomic hydrogen and the hydrogenation by thermal diffusion thereof are performed not in the amorphous silicon film formation but in a separate annealing step. The substrate temperature can be lowered. In addition, since hydrogen is easily desorbed at a low temperature when the substrate temperature is lowered (for example, 200 ° C. or lower), it is preferable in the present invention to lower the film formation temperature of amorphous silicon. Therefore, in the present invention, BT stress is further reduced.
以上述べたように、本発明を応用すれば、ON電流が大
きく、OFF電流が小さく、サブスレッシュホルド領域の
立ち上がりが急峻で、信頼性の優れた薄膜トランジスタ
をプラズマ損傷等による不良を皆無にして製造可能とな
る。更に、本発明によれば、大面積の基板を水素化する
ことも容易である上、量産性も向上するという大きな利
点がある。As described above, by applying the present invention, a thin-film transistor having a large ON current, a small OFF current, a steep rise of a sub-threshold region, and excellent reliability can be manufactured without any defects such as plasma damage. It becomes possible. Further, according to the present invention, there is a great advantage that hydrogenation of a large-area substrate is easy and mass productivity is improved.
本発明の応用としては、例えば、非単結晶シリコンを
素子材としたTFTによって構成された液晶表示パネル、
密着型イメージセンサー、ドライバー内蔵型のサーマル
ヘッド、有機系EL等を発光素子としたドライバー内蔵型
の光書き込み素子や表示素子、三次元IC等が考えられ
る。本発明を用いることで、これらの素子の高速、高解
像度化等の高性能化が実現される。更に、実施例で説明
したように、600℃程度以下の低温プロセスに本発明を
応用することにより、基板として安価なガラスを用いた
大面積で高性能な半導体装置も実現可能となる。As an application of the present invention, for example, a liquid crystal display panel configured by TFT using non-single-crystal silicon as an element material,
A contact-type image sensor, a thermal head with a built-in driver, an optical writing element and a display element with a built-in driver using an organic EL as a light emitting element, a three-dimensional IC, and the like can be considered. By using the present invention, high performance such as high speed and high resolution of these elements is realized. Further, as described in the embodiment, by applying the present invention to a low-temperature process of about 600 ° C. or less, a large-area, high-performance semiconductor device using inexpensive glass as a substrate can be realized.
更に、少なくともゲート絶縁膜とチャンネル領域を成
す非単結晶シリコン層をプラズマCVD法等で真空を破ら
ずに連続形成し、固相成長アニールを行い本発明による
方法で水素化を行うことで、Si/SiO2界面準位密度の低
い(1〜3×1011cm-2程度)poly−SiTFTを再現性良く
形成できるようになった。Furthermore, at least a non-single-crystal silicon layer forming a channel region with a gate insulating film is continuously formed without breaking a vacuum by a plasma CVD method or the like, solid-phase growth annealing is performed, and hydrogenation is performed by the method according to the present invention. A poly-Si TFT having a low / SiO 2 interface state density (about 1 to 3 × 10 11 cm −2 ) can be formed with good reproducibility.
また、本発明は基本的にa−SiTFTの製造プロセスに
固相成長アニールを付加するだけで、高性能なpoly−Si
TFTを形成できるという極めて大きな特徴を有する。従
って、基板の大型化(例えば35cm角以上)や製造コスト
の低減等に対しても大きな効果があるほか、a−SiTFT
のラインを兼用して、poly−SiTFTを形成することがで
き、製造ライン新設のための新規の巨額の投資がいらな
い等のメリットもある。In addition, the present invention basically provides a high-performance poly-Si TFT by simply adding solid phase growth annealing to the a-Si TFT manufacturing process.
It has an extremely large feature that a TFT can be formed. Therefore, it has a great effect on the enlargement of the substrate (for example, 35 cm square or more) and the reduction of the manufacturing cost.
The poly-Si TFT can be formed by also using the above-mentioned line, and there is an advantage that there is no need for a huge new investment for establishing a new production line.
尚、本発明は第1図の実施例に限定されるものではな
く、チャンネル領域の少なくとも一部が多結晶である絶
縁ゲート型電界効果トランジスタ全てに対して有効であ
る。また、チャンネル領域の少なくとも一部が微結晶で
あるトランジスタや、スパッタ法や蒸着法等で形成した
水素化が不十分な非晶質半導体がチャンネル領域の一部
を成すトランジスタにおいても本発明は有効である。ま
た、逆スタガー型のTFTに限らず、トップゲート型のTFT
に対しても本発明は有効である。更に、低温プロセスば
かりでなく、例えば、石英基板を用いた高温プロセスや
三次元IC等に対しても本発明は有効である。The present invention is not limited to the embodiment shown in FIG. 1, but is effective for all insulated gate field effect transistors in which at least a part of the channel region is polycrystalline. The present invention is also effective in a transistor in which at least a part of a channel region is microcrystalline or a transistor in which an amorphous semiconductor which is insufficiently hydrogenated and formed by a sputtering method, an evaporation method, or the like forms a part of a channel region. It is. In addition to the inverted stagger type TFT, a top gate type TFT
The present invention is also effective against the above. Further, the present invention is effective not only in a low-temperature process but also in, for example, a high-temperature process using a quartz substrate or a three-dimensional IC.
また、チャンネル領域が単結晶であっても、再結晶化
または固相成長させたシリコン層に素子を形成する場
合、結晶内に亜粒界等の欠陥を生じ易い。その場合、本
発明に基づく半導体装置の製造方法で、欠陥の終端化を
行うと特性の向上に効果がある。Further, even when the channel region is a single crystal, when an element is formed in a recrystallized or solid phase grown silicon layer, defects such as sub-grain boundaries are easily generated in the crystal. In that case, when the termination of the defect is performed in the method of manufacturing a semiconductor device according to the present invention, there is an effect of improving the characteristics.
さらに、HBT(ヘテロバイポーラトランジスタ)等の
ヘテロ接合界面の欠陥密度の低減に対しても本発明は有
効である。特に、ヘテロ接合を形成する二つの半導体層
のうちの少なくとも一方が、非単結晶半導体よりなる場
合は、本発明によるプラズマ処理により、膜中及び界面
の欠陥を同時に低減することが出来る。Further, the present invention is also effective for reducing the defect density at the interface of a heterojunction such as HBT (hetero bipolar transistor). In particular, when at least one of the two semiconductor layers forming a heterojunction is formed of a non-single-crystal semiconductor, the plasma treatment according to the present invention can reduce defects in the film and at the interface at the same time.
また、非単結晶半導体を素子材とした太陽電池・光セ
ンサやバイポーラトランジスタ、静電誘導トランジスタ
をはじめとして本発明は幅広く半導体プロセス全般に応
用することができる。In addition, the present invention can be widely applied to all semiconductor processes, including solar cells and optical sensors, bipolar transistors, and electrostatic induction transistors using a non-single-crystal semiconductor as an element material.
[発明の効果] 以上述べたように、本発明によればpoly−SiTFT等の
チャンネル領域の少なくとも一部が非単結晶半導体によ
りなる絶縁ゲイト型電界効果トランジスタの高性能化
を、プラズマ損傷等による不良もなく簡便な製造プロセ
スで実現できる。また、本発明は絶縁ゲイト型電界効果
トランジスタに限らず、半導体プロセス全般に渡り広く
応用することができ、その効果はきわめて大きい。[Effects of the Invention] As described above, according to the present invention, the performance of an insulated gate field effect transistor in which at least a part of a channel region such as a poly-Si TFT is made of a non-single-crystal semiconductor is improved by plasma damage or the like. It can be realized by a simple manufacturing process without defects. Further, the present invention can be widely applied not only to the insulated gate field effect transistor but also to all semiconductor processes, and the effect is extremely large.
また本発明によれば、低温プロセスで、電界効果移動
度が高く、界面準位密度が低い、高性能なpoly−SiTFT
を大面積基板(例えば35cm角)上に再現性良く形成する
ことができる。According to the present invention, a high-performance poly-Si TFT having a high field-effect mobility, a low interface state density, and a low-temperature process is provided.
Can be formed on a large area substrate (for example, 35 cm square) with good reproducibility.
従って、走査回路と光電変換素子と同一基板上に集積
化した密着型イメージセンサに本発明を応用した場合に
は、密着型イメージセンサの長尺化に対して有効であ
る。従来複数のチップをインラインに接続していたもの
を、例えば、A3を1本のチップで形成することも可能と
なる。更に、読み取り速度の高速化、高解像場、高階調
化に対しても大きな効果がある。Therefore, when the present invention is applied to a contact type image sensor in which a scanning circuit and a photoelectric conversion element are integrated on the same substrate, it is effective to increase the length of the contact type image sensor. Conventionally, a plurality of chips are connected in-line. For example, A3 can be formed by one chip. Furthermore, there is a great effect on increasing the reading speed, high resolution field, and high gradation.
また、本発明を液晶表示パネルに応用した場合も、大
面積化、低コスト化が可能となるほか、電界効果移動度
の向上にともなって、ドライバーの内蔵や高解像度化も
実現される。Also, when the present invention is applied to a liquid crystal display panel, the area can be increased, the cost can be reduced, and the built-in driver and the high resolution can be realized with the improvement of the field effect mobility.
また、ゲート配線に結晶粒径の大きい多結晶シリコン
を用いることで、ゲート配線抵抗の低減が可能となり、
液晶表示パネルやイメージセンサの大型化に対して、大
きな効果がある。Also, by using polycrystalline silicon having a large crystal grain size for the gate wiring, the gate wiring resistance can be reduced,
This has a great effect on increasing the size of liquid crystal display panels and image sensors.
この他にも、本発明は、TFT駆動液晶シャッタアレ
イ、TFT駆動サーマルヘッド等への応用もまた可能であ
る。また、TFTへの応用ばかりでなく、3次元IC等への
応用に対しても、本発明は有効である。In addition, the present invention is also applicable to a TFT drive liquid crystal shutter array, a TFT drive thermal head, and the like. The present invention is effective not only for application to TFTs but also for applications to three-dimensional ICs and the like.
第1図(a)〜(f)は本発明の半導体装置の製造工程
図である。 101……絶縁材料 102……ゲート電極 103……ゲート絶縁膜 104……非単結晶シリコン層 105……不純物をドープした非単結晶シリコン層 106……キャップ層 107……ドレイン領域 108……ソース領域 109……ドレイン電極 110……ソース電極 111……パッシベーション層1 (a) to 1 (f) are manufacturing process diagrams of a semiconductor device according to the present invention. 101 insulating material 102 gate electrode 103 gate insulating film 104 non-single-crystal silicon layer 105 non-single-crystal silicon layer doped with impurities 106 cap layer 107 drain region 108 source Region 109 Drain electrode 110 Source electrode 111 Passivation layer
Claims (1)
チャンネル領域となる非単結晶シリコン層と、ソース・
ドレイン領域となる不純物がドープされた非単結晶半導
体層とをこの順で形成し、 前記非単結晶半導体層上に水素の拡散を防止するキャッ
プ層を形成して熱処理することにより、前記非単結晶半
導体層から脱離した水素によって前記非単結晶シリコン
層の水素化を行うことを特徴とする半導体装置の製造方
法。A gate electrode, a gate insulating film,
A non-single-crystal silicon layer serving as a channel region and a source /
Forming a non-single-crystal semiconductor layer doped with an impurity to be a drain region in this order; forming a cap layer on the non-single-crystal semiconductor layer to prevent diffusion of hydrogen; A method for manufacturing a semiconductor device, comprising hydrogenating the non-single-crystal silicon layer with hydrogen released from a crystalline semiconductor layer.
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|---|---|---|---|
| JP9690990A JP2874271B2 (en) | 1990-04-12 | 1990-04-12 | Method for manufacturing semiconductor device |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9690990A JP2874271B2 (en) | 1990-04-12 | 1990-04-12 | Method for manufacturing semiconductor device |
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| Publication Number | Publication Date |
|---|---|
| JPH03293731A JPH03293731A (en) | 1991-12-25 |
| JP2874271B2 true JP2874271B2 (en) | 1999-03-24 |
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|---|---|---|---|---|
| JP3344072B2 (en) * | 1994-03-31 | 2002-11-11 | ソニー株式会社 | Method for manufacturing thin film transistor |
| JP3184771B2 (en) * | 1995-09-14 | 2001-07-09 | キヤノン株式会社 | Active matrix liquid crystal display |
| JP2010016072A (en) * | 2008-07-02 | 2010-01-21 | Canon Inc | Thin-film transistor |
| KR101761634B1 (en) * | 2010-10-19 | 2017-07-27 | 삼성디스플레이 주식회사 | Thin film transistor substrate and method for manufacturing thereof |
| JP2014165354A (en) * | 2013-02-26 | 2014-09-08 | Panasonic Corp | Porous silicon manufacturing method |
-
1990
- 1990-04-12 JP JP9690990A patent/JP2874271B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH03293731A (en) | 1991-12-25 |
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