JP3036037B2 - Method for manufacturing semiconductor device - Google Patents
Method for manufacturing semiconductor deviceInfo
- Publication number
- JP3036037B2 JP3036037B2 JP2266956A JP26695690A JP3036037B2 JP 3036037 B2 JP3036037 B2 JP 3036037B2 JP 2266956 A JP2266956 A JP 2266956A JP 26695690 A JP26695690 A JP 26695690A JP 3036037 B2 JP3036037 B2 JP 3036037B2
- Authority
- JP
- Japan
- Prior art keywords
- forming
- polycrystalline silicon
- film
- silicon layer
- annealing
- 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 - Lifetime
Links
- 239000004065 semiconductor Substances 0.000 title claims description 25
- 238000004519 manufacturing process Methods 0.000 title claims description 11
- 238000000034 method Methods 0.000 title description 31
- 238000000137 annealing Methods 0.000 claims description 20
- 229910052710 silicon Inorganic materials 0.000 claims description 17
- 239000000758 substrate Substances 0.000 claims description 17
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 16
- 239000010703 silicon Substances 0.000 claims description 16
- 239000012535 impurity Substances 0.000 claims description 14
- 238000000059 patterning Methods 0.000 claims description 2
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 52
- 239000010408 film Substances 0.000 description 37
- 239000000460 chlorine Substances 0.000 description 13
- 239000012495 reaction gas Substances 0.000 description 11
- 238000002425 crystallisation Methods 0.000 description 7
- 230000008025 crystallization Effects 0.000 description 7
- 229910021417 amorphous silicon Inorganic materials 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 239000007790 solid phase Substances 0.000 description 6
- 230000004913 activation Effects 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 238000009792 diffusion process Methods 0.000 description 4
- 229910052731 fluorine Inorganic materials 0.000 description 4
- 238000002955 isolation Methods 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 3
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 238000005468 ion implantation Methods 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000010409 thin film Substances 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- 230000003213 activating effect Effects 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 230000010354 integration Effects 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910003902 SiCl 4 Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- SLLGVCUQYRMELA-UHFFFAOYSA-N chlorosilicon Chemical compound Cl[Si] SLLGVCUQYRMELA-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- ZOCHARZZJNPSEU-UHFFFAOYSA-N diboron Chemical compound B#B ZOCHARZZJNPSEU-UHFFFAOYSA-N 0.000 description 1
- MROCJMGDEKINLD-UHFFFAOYSA-N dichlorosilane Chemical compound Cl[SiH2]Cl MROCJMGDEKINLD-UHFFFAOYSA-N 0.000 description 1
- BUMGIEFFCMBQDG-UHFFFAOYSA-N dichlorosilicon Chemical compound Cl[Si]Cl BUMGIEFFCMBQDG-UHFFFAOYSA-N 0.000 description 1
- PZPGRFITIJYNEJ-UHFFFAOYSA-N disilane Chemical compound [SiH3][SiH3] PZPGRFITIJYNEJ-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 230000005669 field effect Effects 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 238000005224 laser annealing Methods 0.000 description 1
- 238000004518 low pressure chemical vapour deposition Methods 0.000 description 1
- 229910021424 microcrystalline silicon Inorganic materials 0.000 description 1
- 238000005268 plasma chemical vapour deposition Methods 0.000 description 1
- 238000009832 plasma treatment Methods 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
Landscapes
- Bipolar Transistors (AREA)
- Metal-Oxide And Bipolar Metal-Oxide Semiconductor Integrated Circuits (AREA)
- Semiconductor Memories (AREA)
- Junction Field-Effect Transistors (AREA)
- Thin Film Transistor (AREA)
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は、半導体装置及びその製造方法に係わり、特
に、積層型の半導体装置を形成する製造方法に関する。Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a semiconductor device and a method of manufacturing the same, and more particularly, to a method of forming a stacked semiconductor device.
[従来の技術] 近年、半導体素子の高集積化が進み、4MDRAM、1MSRAM
等の量産や16M、64MDRAM、4MSRAM等の開発・試作が活発
に行われている。今後、これらの半導体素子の高密度化
が更に進むにつれて、三次元構造の半導体素子実現に対
する期待が更に高まるものと予想される。SRAMを例にと
ると、4M以上のSRAMでは、メモリーセルに高抵抗poly−
Siを用いた4−T型のSRAMやシリコン基板上にnチャン
ネルとpチャンネルのMOSFETを形成した6−T型のSRAM
に代わり、積層CMOS構造のSRAMが検討、試作されてい
る。積層COMS構造では、シリコン基板上にnチャンネル
MOSFETが形成され、絶縁材料を挟んでpチャンネルpoly
−SiTFTが積層された構造になっており、4−T型と6
−T型の長所を持ち合わせている。即ち、pチャンネル
をpoly−SiTFTで形成し、積層構造とすることで4−T
型とほぼ同じセルサイズでCMOS構造を実現でき、高集積
性、ソフトエラー耐性、低消費電力性等に優れたSRAMが
実現できる。[Prior Art] In recent years, the integration of semiconductor elements has been advanced, and 4MDRAM, 1MSRAM
The mass production of 16M, 64MDRAM, 4MSRAM, etc. are being actively developed and prototyped. In the future, as the density of these semiconductor devices further increases, it is expected that expectations for the realization of semiconductor devices having a three-dimensional structure will further increase. Taking SRAM as an example, in a 4M or larger SRAM, a high-resistance poly-
4-T type SRAM using Si or 6-T type SRAM with n-channel and p-channel MOSFETs formed on silicon substrate
Instead, an SRAM with a stacked CMOS structure has been studied and prototyped. In a stacked COMS structure, an n-channel
MOSFET is formed and p-channel poly
-SiTFT layered structure, 4-T type and 6
-Has the advantages of the T type. That is, the p-channel is formed of poly-Si TFT, and the p-channel
A CMOS structure can be realized with almost the same cell size as the die, and an SRAM excellent in high integration, soft error resistance, low power consumption, etc. can be realized.
[発明が解決しようとする課題] ところが、従来のpoly−SiTFTを積層した半導体素子
では、以下に述べる問題点があった。(1)poly−Si膜
をLPCVD法で590℃〜630℃程度で成膜するか、固相成長
法poly−Si膜を結晶成長させる方法がおもに用いられて
いたが、この様な方法で形成したpoly−Si膜の結晶性は
必ずしも良好では無く、結晶化率が95%を越える膜や結
晶粒内にtwin等の欠陥が少ない高品質のpoly−Si膜を低
温で形成することか困難であった。そのため、TFTのオ
フ電流の低減、オン電流の増大が困難となっていた。
(2)poly−SiTFTのソース・ドレイン領域をイオンイ
ンプラ法で形成し、600℃〜900℃程度で活性化する方法
が一般に用いられていたが、この方法では活性化アニー
ル時に不純物が横方向に拡散し、実効チャンネル長を減
少させるために、ゲート長1μm以下のTFTを再現性良
く形成することが困難であった。又、チャンネル領域を
成す多結晶シリコン層の膜厚は、500Å程度以下、望ま
しくは50Å〜250Å程度まで薄膜化することで、オフ電
流の低減、Vthの低減等の高性能化が実現できる。とこ
ろが、この様な薄膜にソース・ドレイン領域を形成した
場合、シート抵抗を十分に下げることができない等の問
題もある。[Problems to be Solved by the Invention] However, the conventional semiconductor device in which poly-Si TFTs are stacked has the following problems. (1) A method of forming a poly-Si film at about 590 ° C. to 630 ° C. by LPCVD or a method of growing a poly-Si film by a solid phase growth method has been mainly used. The crystallinity of the obtained poly-Si film is not always good, and it is difficult to form a high-quality poly-Si film having a crystallization ratio of more than 95% or a high-quality poly-Si film having few defects such as twins in crystal grains at a low temperature. there were. Therefore, it has been difficult to reduce the off-state current and increase the on-state current of the TFT.
(2) The method of forming source / drain regions of a poly-Si TFT by an ion implantation method and activating it at about 600 ° C. to 900 ° C. has been generally used. However, in this method, impurities are horizontally transferred during activation annealing. In order to diffuse and reduce the effective channel length, it has been difficult to form a TFT with a gate length of 1 μm or less with good reproducibility. Further, by reducing the thickness of the polycrystalline silicon layer forming the channel region to about 500 ° or less, preferably to about 50 ° to 250 °, high performance such as reduction of off-current and Vth can be realized. However, when the source / drain regions are formed in such a thin film, there is a problem that the sheet resistance cannot be sufficiently reduced.
そこで、本発明はより簡便かつ実用的な方法で、結晶
性の高い多結晶シリコンを低温で再現性良く形成し、高
性能なpoly−SiTFTを低温形成する方法を提供するもの
である。更に、本発明はゲート長1μm以下の微細なpo
ly−SiTFTを形成する方法も提供する。Therefore, the present invention provides a simpler and more practical method for forming polycrystalline silicon having high crystallinity at low temperature with good reproducibility and forming a high-performance poly-Si TFT at low temperature. Further, the present invention provides a fine po
A method for forming a ly-Si TFT is also provided.
[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、基板上にゲート電
極を形成する工程と、前記ゲート電極上にゲート絶縁膜
をなす絶縁膜を形成する工程と、前記絶縁膜上にソース
・ドレイン領域となる第1シリコン層を形成する工程
と、前記ゲート電極上の第1シリコン層を取り除くよう
にパターニングする工程と、前記第1シリコン層をアニ
ールして不純物を活性化させる工程とを有し、しかる後
に前記ゲート電極上及び前記第1シリコン層上にチャネ
ルとなる第2シリコン層を形成することを特徴とする。[Means for Solving the Problems] In a method for manufacturing a semiconductor device according to the present invention, a step of forming a gate electrode on a substrate, a step of forming an insulating film forming a gate insulating film on the gate electrode, Forming a first silicon layer serving as a source / drain region on the film; patterning the first silicon layer on the gate electrode so as to remove the first silicon layer; annealing the first silicon layer to activate impurities And then forming a second silicon layer to be a channel on the gate electrode and the first silicon layer.
[実施例] 第3図は、従来の半導体装置の断面図の一例である。
尚、第3図では半導体素子としてスタックト型CMOSを例
としている。第3図において、301はシリコン基板、302
はp−well領域、303はLOCOS酸化法で形成した素子分離
領域、304はゲート絶縁膜、305poly−Si等を素子材とし
たゲート電極、306はn+拡散領域、307はゲート絶縁膜
を成す絶縁層、308はチャンネル領域を成す多結晶シリ
コン層、309はソース・ドレイン領域を成すp+拡散領
域であり、イオンインプラ法でボロンを打ち込んだ後、
600℃〜900℃程度で活性化する方法が一般に用いられて
いる。しかし、この方法では活性化アニール時に不純物
が横方向に拡散し、実効チャンネル長を減少させるため
に、ゲート長1μm以下のTFTを再現性良く形成するこ
とが困難であった。又、チャンネル領域を成す多結晶シ
リコン層の膜厚は、500Å程度以下、望ましくは50Å〜2
50Å程度まで薄膜化することで、オフ電流の低減、Vth
の低減等の高性能化が実現できる。ところが、従来の素
子構造では、前述の理由で多結晶シリコン膜を薄膜化し
た場合、ソース・ドレイン領域のシート抵抗を十分に下
げることができない等の問題もあった。本発明はこの様
な問題を解決するもので、以下、その詳細を実施例に基
づき説明する。FIG. 3 is an example of a cross-sectional view of a conventional semiconductor device.
In FIG. 3, a stacked type CMOS is taken as an example of the semiconductor element. In FIG. 3, 301 is a silicon substrate, 302
Is a p-well region, 303 is an element isolation region formed by the LOCOS oxidation method, 304 is a gate insulating film, 305 a gate electrode using poly-Si or the like as an element material, 306 is an n + diffusion region, and 307 is an insulating material forming a gate insulating film. Layer, 308 is a polycrystalline silicon layer forming a channel region, 309 is ap + diffusion region forming a source / drain region, and after implanting boron by ion implantation,
A method of activating at about 600 ° C. to 900 ° C. is generally used. However, in this method, impurities are diffused in the lateral direction during activation annealing and the effective channel length is reduced, so that it is difficult to form a TFT having a gate length of 1 μm or less with good reproducibility. The thickness of the polycrystalline silicon layer forming the channel region is about 500 ° or less, preferably 50 ° to 2 °.
By reducing the film thickness to about 50 °, the off-current can be reduced and Vth
Higher performance such as reduction of noise can be realized. However, in the conventional element structure, when the polycrystalline silicon film is thinned for the above-described reason, there is a problem that the sheet resistance of the source / drain regions cannot be sufficiently reduced. The present invention solves such a problem, and details thereof will be described below based on embodiments.
第1図は、本発明の実施例における半導体装置の断面
図の一例である。尚、第1図では半導体素子としてスタ
ックト型CMOSを例としている。第1図において、101は
シリコン基板、102はp−well領域、103はLOCOS酸化法
で形成した素子分離領域、104はゲート絶縁膜、105poly
−Si等を素子材としたゲート電極、106はn+拡散領
域、107はゲート絶縁膜を成す絶縁層、109ソース・ドレ
イン領域を成す不純物をドープした多結晶シリコン層、
108はチャンネル領域を成す多結晶シリコン層である。
本発明では、poly−SiTFTのソース・ドレイン領域を不
純物をドープした多結晶シリコン層で形成するため、活
性化アニール時に不純物が横方向に拡散し、実効チャン
ネル長を減少させる問題も起きず、ゲート長1μm以下
のTFTを再現性良く形成することができるようになっ
た。即ち、本発明の積層構造のTFTでは、フォト工程の
パターン精度のみに依存して、実効チャンネル長を制御
できるため、サブミクロンのpoly−SiTFTを再現性良く
形成することができる。又、チャンネル領域を成す多結
晶シリコン層の膜厚は、500Å程度以下、望ましくは50
Å〜250Å程度まで薄膜化することで、オフ電流の低
減、Vthの低減等の高性能化が実現できる。ところが、
従来の構造ではチャンネル領域の多結晶シリコンと同一
の薄膜にソース・ドレイン領域を形成する構造のため、
シート抵抗が高くなるという問題もあった。しかし、本
発明ではソース・ドレイン領域をチャンネル領域とは別
に形成するため、チャンネル領域の膜厚とソース・ドレ
イン領域の膜厚を独立に設定でき、上述の問題を回避す
ることができる。FIG. 1 is an example of a cross-sectional view of a semiconductor device according to an embodiment of the present invention. FIG. 1 shows a stacked CMOS as an example of the semiconductor element. In FIG. 1, 101 is a silicon substrate, 102 is a p-well region, 103 is an element isolation region formed by LOCOS oxidation, 104 is a gate insulating film, 105 poly.
A gate electrode using -Si or the like as an element material; 106, an n + diffusion region; 107, an insulating layer forming a gate insulating film; 109, a polycrystalline silicon layer doped with impurities forming source / drain regions;
108 is a polycrystalline silicon layer forming a channel region.
In the present invention, since the source / drain regions of the poly-Si TFT are formed of a polycrystalline silicon layer doped with an impurity, the impurity does not diffuse laterally during activation annealing, and there is no problem that the effective channel length is reduced. TFTs having a length of 1 μm or less can be formed with good reproducibility. That is, in the TFT having a laminated structure according to the present invention, the effective channel length can be controlled only depending on the pattern accuracy of the photo process, so that a submicron poly-Si TFT can be formed with high reproducibility. The thickness of the polycrystalline silicon layer forming the channel region is about 500 mm or less, preferably 50 mm or less.
By reducing the thickness to about {circle around (2)} to about 250}, high performance such as reduction of off-state current and reduction of Vth can be realized. However,
In the conventional structure, the source / drain region is formed in the same thin film as the polycrystalline silicon in the channel region.
There is also a problem that the sheet resistance becomes high. However, in the present invention, since the source / drain region is formed separately from the channel region, the thickness of the channel region and the thickness of the source / drain region can be set independently, and the above problem can be avoided.
第2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2図では3次元トランジス
タへの簡単な応用例(スタックト型CMOS)を示す。FIG. 2 is an example of a manufacturing process diagram of the semiconductor device according to the embodiment of the present invention. FIG. 2 shows a simple application example (stacked CMOS) to a three-dimensional transistor.
第2図において、(a)は、シリコン基板201にp−w
ell領域202を形成し、LOCOS酸化法で素子分離領域203を
形成する工程である。In FIG. 2, (a) shows p-w on a silicon substrate 201.
This is a step of forming the ell region 202 and forming the element isolation region 203 by the LOCOS oxidation method.
(b)は、ゲート絶縁膜204を形成後、ゲート電極205
をpoly−Si等を素子材とし形成後、所定の形状にパター
ン形成し、ソース・ドレイン領域を成すn+拡散層206を
形成する工程である。(B), after forming the gate insulating film 204, the gate electrode 205
Is formed using poly-Si or the like as an element material, and then patterned into a predetermined shape to form an n + diffusion layer 206 forming source / drain regions.
(c)は、ゲート絶縁膜を成す絶縁層207を形成し、
コンタクトホールを開け、ソース・ドレイン領域を成す
不純物をドープした多結晶シリコン層210を500Å〜4000
Å程度形成し、所定の形状にパターン形成する工程であ
る。多結晶シリコン層の形成方法としては、プラズマCV
D法(PCVD法)で基板温度300℃〜450℃程度の低温で多
結晶シリコンを膜厚500Å〜3500Å程度成膜する方法が
ある。以下に、成膜条件の一例を示す。反応ガスとし
て、モノシラン(SiH4)、ジクロルシラン(SiH2C
l2)、H2を用い、混合比を例えば、SiH4:SiH2Cl2=1:20
〜1:200程度、SiH4:H2=1:100〜1:1000程度に設定し、
ドーピングガスとして、ジボラン(B2H6)等を用い、例
えば、SiH4:B2H6=1:0.002〜1:0.04程度の混合比で混合
する。基板温度を300℃〜450℃程度に保持し、rfパワー
を印加し反応ガスを分解し、不純物をドープした低抵抗
多結晶シリコンを成膜する。この様にして形成された多
結晶シリコンのシート抵抗は1000Åの膜厚で60〜100Ω
/□であり、低抵抗な多結晶シリコンを低温で成膜する
ことができた。又、基板温度を450℃〜600℃程度の比較
的高温で成膜した場合、上述のシート抵抗の値は40〜60
Ω/□程度まで下げることもできる。尚、多結晶シリコ
ンの形成方法はこれに限定されるものではない。例え
ば、固相成長法で低抵抗の多結晶シリコンを形成するこ
ともできる。以下、その一例を説明する。まず、不純物
をドープしたa−Si膜をPCVD法で成膜する。反応ガスは
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、13.56
MHzのrf電源を用いた。B2H6、SiH4の流量比は[B2H6]
/[SiH4]=3×10−3〜4×10−2となるように設定
した。a−Si成膜後、450℃で30min.N2でプリアニール
してa−Si中に含まれるH2を脱離させる。これは、H2が
a−Si中に含まれたまま固相成長アニールを行うと、H2
が抜けた部分が空孔となり、多孔質の膜になってしまう
のを防ぐ目的である。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時間である。この固相成長アニールによって、a−
Si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。これでp+poly−Siができる。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。レーザ
ービーム、ハロゲンランプを用いる場合は、N2アニール
に比べてアニール時間を短縮できる。アニール工程時に
はa−Si成膜時に混入させたB原子も同時に活性化され
る。この結果、多結晶シリコンの抵抗率は、p+poly−
Siで1〜3×10−3Ω・cm程度まで低抵抗化される。次
に、ソース、ドレイン領域の不純物のより完全な活性化
を目的として、700℃〜800℃程度のN2アニール、ランプ
アニールもしくはレーザーアニールを必要に応じて施
す。この活性化アニールにより、B原子の完全な活性化
と結晶化率の増大も同時に達成され、p+poly−Siの抵
抗率は1〜5×10−4Ω・cm(1000Åの膜厚で10〜50Ω
/□)程度まで下げることもできる。(C), forming an insulating layer 207 forming a gate insulating film;
A contact hole is opened, and a polycrystalline silicon layer 210 doped with impurities forming a source / drain region is formed to a thickness of 500 to 4000
工程 This is a step of forming a pattern and forming a pattern in a predetermined shape. As a method for forming the polycrystalline silicon layer, plasma CV
There is a method of forming a polycrystalline silicon film with a film thickness of about 500 to 3500 at a low temperature of about 300 ° C. to about 450 ° C. by a D method (PCVD method). The following is an example of the film forming conditions. Monosilane (SiH 4 ), dichlorosilane (SiH 2 C)
l 2 ) and H 2 , and the mixing ratio is, for example, SiH 4 : SiH 2 Cl 2 = 1: 20
To 1: about 200, SiH 4: H 2 = 1: 100~1: set to about 1000,
Diborane (B 2 H 6 ) or the like is used as a doping gas, and for example, SiH 4 : B 2 H 6 is mixed at a mixing ratio of about 1: 0.002 to 1: 0.04. The substrate temperature is maintained at about 300 ° C. to 450 ° C., rf power is applied to decompose the reaction gas, and a low-resistance polycrystalline silicon doped with impurities is formed. The sheet resistance of the polycrystalline silicon thus formed is 60 to 100 Ω at a thickness of 1000 mm.
/ □, low-resistance polycrystalline silicon could be formed at a low temperature. When the film is formed at a relatively high substrate temperature of about 450 ° C. to 600 ° C., the above-mentioned sheet resistance value is 40 to 60.
It can be lowered to about Ω / □. The method for forming polycrystalline silicon is not limited to this. For example, low-resistance polycrystalline silicon can be formed by a solid-phase growth method. Hereinafter, an example will be described. First, an a-Si film doped with impurities is formed by a PCVD method. The reaction gas is
SiH4 and H2 gases were used, and B2H6 gas was used as a doping gas. Substrate temperature is 150-250 ° C, internal pressure is 0.8 Torr, 13.56
A MHz rf power supply was used. The flow ratio of B2H6 and SiH4 is [B2H6]
/ [SiH4] = 3 × 10−3 to 4 × 10−2. After forming the a-Si film, pre-annealing is performed at 450 ° C. for 30 min. N2 to remove H2 contained in the a-Si. This is because if solid phase growth annealing is performed while H2 is contained in a-Si, H2
This is for the purpose of preventing the portion from which has been removed from becoming a pore and becoming a porous film. Thereafter, the process proceeds to a solid phase growth annealing step. Annealing conditions are 4 in N2 gas at 550-650 ° C.
~ 72 hours. By this solid phase growth annealing, a-
Si is polycrystallized, and the average grain size of Si grains in the gate electrode is reduced to about 1 to 3 μm, and many grains having a grain size of 5 μm or more appear. This completes p + poly-Si. Annealing is not limited to N2 annealing, but may be laser beam annealing, halogen lamp annealing, or the like. When a laser beam or a halogen lamp is used, the annealing time can be reduced as compared with N2 annealing. During the annealing step, the B atoms mixed in during the a-Si film formation are also activated at the same time. As a result, the resistivity of the polycrystalline silicon is p + poly−
The resistance is reduced to about 1 to 3 × 10 −3 Ω · cm by Si. Next, N2 annealing, lamp annealing, or laser annealing at about 700 ° C. to 800 ° C. is performed as necessary to more completely activate the impurities in the source and drain regions. By this activation annealing, complete activation of B atoms and an increase in the crystallization rate are simultaneously achieved, and the resistivity of p + poly-Si is 1-5 × 10 −4 Ω · cm (10-50 Ω at a thickness of 1000 °).
/ □).
(d)は、ゲート絶縁膜を成す絶縁層207表面の清浄
化を目的としたライトエッチングを行なった後、多結晶
シリコン層208を形成し、続いて、結晶粒界に存在する
欠陥を低減する目的で、水素プラズマ処理等の水素化処
理を行う工程である。多結晶シリコン層の形成方法とし
ては、プラズマCVD法(PCVD法)で基板温度300℃〜450
℃程度の低温で多結晶シリコンを膜厚50Å〜1500Å程度
成膜する方法が有効である。PCVD法では、通常、反応ガ
スとして、モノシラン(SiH4)やジシラン(Si2H6)等
を用いるが、この様な反応ガスを用いた場合、300℃〜4
50℃程度の基板温度では、非晶質シリコンかせいぜい微
結晶シリコンが成膜されるだけであり、高品質な多結晶
シリコンを成膜することは困難である。しかし、反応ガ
スとして、上述のSiH4、Si2H6等に加えて、弗素
(F)、塩素(Cl)等の元素を含む反応ガスを適量混合
することで、高品質な多結晶シリコン膜を低温形成でき
る。反応ガスとして、SiH4、Si2H6等に加えて、弗素
(F)、塩素(Cl)等の元素を含む反応ガスを適量混合
することで、高品質な多結晶シリコン膜を低温形成でき
る。成膜条件の一例を以下に示す。反応ガスとして、Si
H4、ジクロルシラン(SiH2Cl2)、H2を用い、混合比を
例えば、SiH4:SiH2Cl2=1:20〜1:200程度、SiH4:H2=1:
100〜1:1000程度に設定し、基板温度を300℃〜450℃程
度に保持し、rfパワーを印加し、反応ガスを分解し多結
晶シリコンを成膜する。膜厚に関しては、多結晶シリコ
ン層を薄膜化すると、オフ電流が減少し、Vth(しきい
値電圧)が減少する現象が知られている。従って、多結
晶シリコン層の膜厚は500Å以下が望ましく、50Å〜250
Å程度が特に望ましい。従って、この様な薄膜でかつ高
品質な多結晶シリコンを形成することが特に重要とな
る。基板温度が300℃以下の場合は、結晶化率が低く、
<220>配向性も見られないが、基板温度を400℃〜450
℃程度にすると50Å〜250Å程度の薄膜でも、結晶化率9
8%以上で<220>に配向した高品質な多結晶シリコンを
成膜することができる。又、結晶化率を上げるという点
では、基板温度は450℃〜600℃程度で成膜した膜のほう
がさらに良好で、99.5%以上の結晶化率を達成でき、TF
Tのオン電流の増大及びオフ電流の低減に有効である。(D), after performing light etching for the purpose of cleaning the surface of the insulating layer 207 forming the gate insulating film, forming the polycrystalline silicon layer 208, and subsequently reducing defects existing at crystal grain boundaries. This is a step of performing a hydrogenation treatment such as a hydrogen plasma treatment for the purpose. As a method for forming a polycrystalline silicon layer, a substrate temperature of 300 ° C. to 450 ° C. is used by a plasma CVD method (PCVD method).
It is effective to form a polycrystalline silicon film at a low temperature of about 100 ° C. with a film thickness of about 50 ° to 1500 °. In the PCVD method, usually, monosilane (SiH 4 ), disilane (Si 2 H 6 ), or the like is used as a reaction gas.
At a substrate temperature of about 50 ° C., at most microcrystalline silicon of amorphous silicon is formed, and it is difficult to form high-quality polycrystalline silicon. However, by mixing an appropriate amount of a reaction gas containing elements such as fluorine (F) and chlorine (Cl) in addition to the above-mentioned SiH 4 , Si 2 H 6 and the like, a high-quality polycrystalline silicon film is obtained. Can be formed at a low temperature. By mixing an appropriate amount of a reaction gas containing elements such as fluorine (F) and chlorine (Cl) in addition to SiH 4 and Si 2 H 6 as a reaction gas, a high-quality polycrystalline silicon film can be formed at a low temperature. . An example of the film forming conditions is shown below. As a reaction gas, Si
Using H 4 , dichlorosilane (SiH 2 Cl 2 ), and H 2 , the mixing ratio is, for example, about SiH 4 : SiH 2 Cl 2 = 1: 20 to 1: 200, and SiH 4 : H 2 = 1:
The substrate temperature is set at about 100 to 1: 1000, the substrate temperature is maintained at about 300 to 450 ° C., and rf power is applied to decompose the reaction gas to form a polycrystalline silicon film. Regarding the film thickness, it is known that when the thickness of the polycrystalline silicon layer is reduced, the off current decreases and Vth (threshold voltage) decreases. Therefore, the thickness of the polycrystalline silicon layer is desirably 500 ° or less, and
Å is particularly desirable. Therefore, it is particularly important to form such thin film and high quality polycrystalline silicon. When the substrate temperature is 300 ° C or lower, the crystallization rate is low,
<220> No orientation is observed, but the substrate temperature is 400 ° C to 450 ° C.
At a temperature of about 50 ° C, a crystallization rate of 9
At 8% or more, high-quality polycrystalline silicon oriented in <220> can be formed. In terms of increasing the crystallization rate, a film formed at a substrate temperature of about 450 ° C. to 600 ° C. is more favorable, and a crystallization rate of 99.5% or more can be achieved.
This is effective for increasing the ON current of T and reducing the OFF current.
この様に、本発明によれば、低温で高品質の多結晶シ
リコン膜を形成できるため、本実施例に示したスタック
ト型CMOSを始め、高性能な3次元ICを低温で製造するこ
とができる。尚、本実施例では反応ガスとして、SiH2Cl
2を用いる場合を示したが、これに限定されるものでは
ない。例えばSiCl4、SiH2Cl2、SiHCl3、Cl2、SiF4、SiH
F3、SiH2F2、SiH3F、Si2F6、F2、HCl等のF(弗素)も
しくはCl(塩素)のうちの少なくとも一方の元素を含む
エッチング性を有する反応ガスとSiH4、Si2H6、Si3H8等
の反応ガスを適量混合することで、高品質な多結晶シリ
コンを低温で成膜することができる。As described above, according to the present invention, a high-quality polycrystalline silicon film can be formed at a low temperature, so that a high-performance three-dimensional IC including the stacked CMOS shown in this embodiment can be manufactured at a low temperature. . In this example, SiH 2 Cl was used as the reaction gas.
Although the case of using 2 has been described, the present invention is not limited to this. For example, SiCl 4 , SiH 2 Cl 2 , SiHCl 3 , Cl 2 , SiF 4 , SiH
Etching reaction gas containing at least one element of F (fluorine) or Cl (chlorine) such as F 3 , SiH 2 F 2 , SiH 3 F, Si 2 F 6 , F 2 , HCl and SiH 4 By mixing an appropriate amount of a reaction gas such as Si 2 H 6 or Si 3 H 8 , high-quality polycrystalline silicon can be formed at a low temperature.
本発明に基づく半導体装置の製造方法を用い、作成し
た多結晶シリコンTFT(Nチャンネル)の電界効果移動
度は、150〜200cm2/V・sec程度、オンオフ比8〜9桁
(Ion:Vd=5V、Vg=10V、Ioff:Vd=5V、Vg=0V)程度で
あり、高性能なpoly−SiTFTを低温で形成することがで
きた。The field-effect mobility of a polycrystalline silicon TFT (N-channel) formed by using the method of manufacturing a semiconductor device according to the present invention is about 150 to 200 cm 2 / V · sec, and the on / off ratio is 8 to 9 digits (Ion: Vd = 5 V, Vg = 10 V, Ioff: Vd = 5 V, Vg = 0 V), and a high-performance poly-Si TFT could be formed at a low temperature.
又、チャンネル領域に不純物をドーピングして、Vth
(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、Vt
hのシフトを抑えることができる。例えば、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。Also, doping the channel region with an impurity,
Means for controlling (threshold voltage) is also very effective.
In a polycrystalline silicon TFT formed by the solid-phase growth method, Vth of the N-channel transistor tends to shift in the depletion direction, and P-channel transistor tends to shift 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 , Vt
h shift can be suppressed. For example, there is a method in which an impurity such as B (boron) is implanted at a dose of about 10 11 to 10 13 / cm 2 by an ion implantation method or the like.
尚、本発明は、第1図及び第2図の実施例に示したス
タックト型CMOS以外にも、積層型の絶縁ゲート型半導体
素子全般に応用できるほか、バイポーラトランジスタ、
静電誘導型トランジスタ、太陽電池・光センサをはじめ
とする光電変換素子等の半導体素子を多結晶半導体を素
子材として形成する場合にきわめて有効な製造方法とな
る。It should be noted that the present invention can be applied not only to the stacked CMOS shown in the embodiment of FIGS.
This is a very effective manufacturing method when a semiconductor element such as a photoelectric conversion element such as an electrostatic induction transistor, a solar cell or an optical sensor is formed using a polycrystalline semiconductor as an element material.
[発明の効果] 以上述べたように、本発明によればより簡便な製造プ
ロセスで大粒径で結晶化率の高い多結晶シリコン膜を低
温で形成することができる。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、三次元IC等の積層型の半導体装置を低温で簡便なプ
ロセスで製造できるようになった。[Effects of the Invention] As described above, according to the present invention, a polycrystalline silicon film having a large grain size and a high crystallization rate can be formed at a low temperature by a simpler manufacturing process. As a result, a high-performance semiconductor element can be formed on an insulating amorphous material, and a stacked semiconductor device such as a three-dimensional IC can be manufactured at a low temperature by a simple process.
また、本発明は、第1図及び第2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
るほか、バイポーラトランジスタ、静電誘導型トランジ
スタ、太陽電池・光センサをはじめとする光電変換素子
等の半導体素子を多結晶半導体を素子材として形成する
場合にきわめて有効な製造方法となる。In addition, the present invention is shown in the embodiment of FIGS. 1 and 2.
In addition to TFT, it can be applied to insulated gate type semiconductor devices in general, and semiconductor devices such as bipolar transistors, electrostatic induction type transistors, photoelectric conversion devices such as solar cells and optical sensors, etc. are formed using polycrystalline semiconductors as device materials. This is an extremely effective manufacturing method.
第1図は本発明の実施例における半導体装置の断面図で
ある。 第2図(a)〜(d)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。 第3図は従来の半導体装置の断面図である。 101,201,301……シリコン基板 102,202,302……p−well領域 103,203,303……素子分離領域 104,204,304……ゲート絶縁膜 105,205,305……ゲート電極 107,207,307……ゲート絶縁膜 108,208,308……多結晶シリコン層 109,209,309……ソース・ドレイン領域FIG. 1 is a sectional view of a semiconductor device according to an embodiment of the present invention. 2 (a) to 2 (d) are manufacturing process diagrams of a semiconductor device according to an embodiment of the present invention. FIG. 3 is a sectional view of a conventional semiconductor device. 101, 201, 301 ... silicon substrate 102, 202, 302 ... p-well region 103, 203, 303 ... element isolation region 104, 204, 304 ... gate insulating film 105, 205, 305 ... gate electrode 107, 207, 307 ... gate insulating film 108, 208, 308 ... polycrystalline silicon layer 109, 209, 309 ... source / drain region
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI H01L 29/786 (58)調査した分野(Int.Cl.7,DB名) H01L 27/092 H01L 29/784 H01L 27/00 301 H01L 27/10 381 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 identification code FI H01L 29/786 (58) Investigated field (Int.Cl. 7 , DB name) H01L 27/092 H01L 29/784 H01L 27/00 301 H01L 27/10 381
Claims (1)
る工程と、 前記絶縁膜上にソース・ドレイン領域となる第1シリコ
ン層を形成する工程と、 前記ゲート電極上の第1シリコン層を取り除くようにパ
ターニングする工程と、 前記第1シリコン層をアニールして不純物を活性化させ
る工程とを有し、 しかる後に前記ゲート電極上及び前記第1シリコン層上
にチャネルとなる第2シリコン層を形成することを特徴
とする半導体装置の製造方法。A step of forming a gate electrode on the substrate; a step of forming an insulating film forming a gate insulating film on the gate electrode; and forming a first silicon layer serving as a source / drain region on the insulating film. Forming, patterning so as to remove the first silicon layer on the gate electrode, and annealing the first silicon layer to activate impurities. A method of manufacturing a semiconductor device, comprising: forming a second silicon layer serving as a channel on the first silicon layer.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2266956A JP3036037B2 (en) | 1990-10-04 | 1990-10-04 | Method for manufacturing semiconductor device |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2266956A JP3036037B2 (en) | 1990-10-04 | 1990-10-04 | Method for manufacturing semiconductor device |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH04144165A JPH04144165A (en) | 1992-05-18 |
| JP3036037B2 true JP3036037B2 (en) | 2000-04-24 |
Family
ID=17438031
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2266956A Expired - Lifetime JP3036037B2 (en) | 1990-10-04 | 1990-10-04 | Method for manufacturing semiconductor device |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3036037B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR940009608B1 (en) * | 1991-11-30 | 1994-10-15 | 삼성전자 주식회사 | Semiconductor memory device & manufacturing method thereof |
| DE4435461C2 (en) | 1993-10-06 | 2001-09-20 | Micron Technology Inc N D Ges | Thin film transistor and its manufacturing process |
-
1990
- 1990-10-04 JP JP2266956A patent/JP3036037B2/en not_active Expired - Lifetime
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| Publication number | Publication date |
|---|---|
| JPH04144165A (en) | 1992-05-18 |
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