KR100275712B1 - 반도체 소자의 게이트 산화막 형성방법 - Google Patents
반도체 소자의 게이트 산화막 형성방법 Download PDFInfo
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- KR100275712B1 KR100275712B1 KR1019920018695A KR920018695A KR100275712B1 KR 100275712 B1 KR100275712 B1 KR 100275712B1 KR 1019920018695 A KR1019920018695 A KR 1019920018695A KR 920018695 A KR920018695 A KR 920018695A KR 100275712 B1 KR100275712 B1 KR 100275712B1
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- 239000004065 semiconductor Substances 0.000 title claims abstract description 10
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 claims abstract description 11
- 238000004518 low pressure chemical vapour deposition Methods 0.000 claims abstract description 7
- 230000001698 pyrogenic effect Effects 0.000 claims abstract description 3
- 239000000758 substrate Substances 0.000 claims description 7
- 238000001004 secondary ion mass spectrometry Methods 0.000 abstract description 7
- 238000004458 analytical method Methods 0.000 abstract description 6
- 238000006243 chemical reaction Methods 0.000 abstract description 5
- 230000015556 catabolic process Effects 0.000 abstract description 4
- 239000010453 quartz Substances 0.000 abstract description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 4
- 239000012495 reaction gas Substances 0.000 abstract description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 15
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 8
- 229910052710 silicon Inorganic materials 0.000 description 8
- 239000010703 silicon Substances 0.000 description 8
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 5
- 229920005591 polysilicon Polymers 0.000 description 5
- 230000007547 defect Effects 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 description 2
- 229910006367 Si—P Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000007772 electrode material Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000009279 wet oxidation reaction Methods 0.000 description 1
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Abstract
본 발명은 MOS소자의 게이트 산화막과 같은 얇은 산화막 형성방법에 관한 것이다.
본 발명은 반도체소자에 사용되는 게이트 산화막의 형성방법에 있어서, 반도체기판상에 저압 화학기상 증착방법을 사용하여 제 1 게이트산화막으로 HTO막을 성장시킨 후, 상기 제 1 게이트 산화막위에 제 2게이트 산화막으로 습식산화막을 성장시켜 게이트 산화막을 형성하는 것을 특징으로 하는 반도체소자의 게이트 산화막 형성방법을 제공한다.
본 발명에 의하면, 우수한 전기적 특성을 갖는 좋은 막질의 게이트 산화막을 형성할 수 있다.
Description
제1a도 내지 제1c도는 종래의 산화막과 본 발명의 게이트 산화막 각각의 T.D.D.B특성을 나타낸 것이고,
제2a도 내지 제2c도는 종래의 산화막과 본 발명의 게이트 산화막 각각의 I-V특성을 나타낸 것이고,
제3a도 내지 제3c도는 종래의 산화막과 본 발명의 게이트 산화막 각각의 SIMS분석결과를 나타낸 것이다.
본 발명은 반도체 소자의 절연막 형성방법에 관한 것으로, 반도체 소자의 게이트 산화막 형성방법에 관한 것이다.
반도체 소자의 고집적화에 비례하여 MOS소자의 절연막으로 사용되고 있는 얇은 산화막의 두께 또한 점점 얇아지고 있지만 산화막에 인가되는 전압은 감소되지 않는다. 따라서 이러한 얇은 산화막은 미세한 결합에 민감하게 반응을 하기 때문에 결함에 오래 견디는 특성을 가진 산화막을 만드는 것이 필요하다.
MOS소자에 사용되고 있는 얇은 산화막의 종류는 여러가지이다. 이중, O2만을 이용하거나 또는 O2+ HC1을 이용하여 형성하는 건식산화막에는 미세기공(micropore)이나 보이드(void)와 같은 결함이 존재하는 것으로 알려져 있고, 습식산화막의 경우는 전기적특성은 우수하나, 게이트 산화막으로 사용할 경우, 게이트 전극물질인 폴리실리콘에 POCl3을 주입했을 때 폴리실리콘의 Si원자와 POCl3의 P-이온이 반응하여 Si-P부피팽창의 결과로 게이트 산화막과 폴리실리콘 계면에 스트레스를 주게 되고, 폴리실리콘 하부의 게이트 산화막이 결합력이 약해지면서 계면에 쌓여 있는 P-이온과 게이트 산화막의 Si가 반응하여 결국 게이트 산화막과 폴리실리콘 계면에서 게이트 산화막의 소모가 일어나게 되어 게이트 산화막의 내압 특성이 나빠지는 것으로 알려져 있다. 또한 상기 건식산화막과 습식산화막은 실리콘 배어웨이퍼(Bare wafer)에 존재하는 미세한 피팅(pitting)에 대한 내성이 없다.
따라서 MOS집적소자의 커패시터절연막 또는 게이트산화막에 적용할 경우 산화막 자체의 신뢰성저하에 따라 소자의 수율에 나쁜 영향을 미치게 된다.
또한, HTO(High Temperature Oxide)의 경우는 상기 건식산화막과 습식산화막등의 열산화막과는 달리 실리콘 표면의 조건에 상관없이 증착(Deposition)방법으로 성장시키는 막으로서 하부막에 영향을 주지 않는 산화막으로 널리 사용되고 있으나, T.D.D.B(Time Dependence Dielectric Breakdown Voltage)특성과 I-V특성이 좋지 않은 단점이 있다.
따라서 본 발명은 상기한 종래의 산화막의 단점을 극복한 고품질의 게이트 산화막을 형성함으로써 반도체소자에의 적용시 신뢰성을 향상시키는 것을 그 목적으로 한다.
상기 목적을 달성하기 위해 본 발명에 의한 게이트 산화막 형성방법은 실리콘기판위에 제 1 게이트 산화막으로 LPCVD(Low Pressure Chemical Vapor Deposition)법을 이용하여 성장시킨 HTO막을 형성하고, 이어서 제 1 게이트 산화막위에 제 2 게이트 산화막으로 습식산화를 이용하여 성장시킨 습식산화막을 형성하는 것을 특징으로 한다.
상기 제 1 게이트 산화막은 LPCVD법을 이용하여 압력 0.5Torr, 온도 750℃∼850℃에서 SiH4가스와 N2O가스를 반응시켜 50Å∼200Å 두께로 형성한다.
상기 제 2 게이트 산화막은 800℃∼900℃에서 통상의 석영반응관(Quartz tube)를 이용하여 발열시스템(Pyrogenic system)에서 50Å∼200Å 두께로 형성한다.
상기와 같이 HTO의 장점인 막질의 균일성과 산화막 성장전의 청정상태에 무관하게 성장시킬 수 있는 점, 그리고 증착방식에 따른 실리콘기판 표면에 존재하는 미세한 미팅들을 보상해 줄 수 있는 유리한 면이 있는 제 1 게이트 산화막과, 습식산화막의 장점인 산화막내의 스트레스완화 및 우수한 전기적 특성을 갖는 제 2 게이트 산화막을 조합하여 게이트 산화막을 형성함으로써 게이트 산화막의 막질을 향상시킬 수 있으며, MOS소자에의 적용시 소자의 신뢰성을 확보할 수 있다.
이하, 본 발명의 일실시예를 설명한다.
본 발명의 효과를 명확하게 설명하기 위해 종래의 열산화막과 HTO산화막의 형성방법에 의해 형성된 산화막의 특성을 비교예를 들고, 이를 본 발명의 일실시예에 의한 게이트 산화막 형성방법에 의해 형성된 산화막의 특성과 비교하여 설명하면 다음과 같다.
[비교예 1]
통상의 석영반응관내에서 950℃에서 O2+ HCl(1%)을 이용하여 건식산화하여 200Å두께의 열산화막을 형성한다.
[비교예 2]
통상의 LPCVD 반응관내에서 온도 750℃∼850℃, 압력 0.5Torr, 반응가스 SiH4, N2O를 이용하여 200Å두께의 HTO를 형성한다.
[실시예]
제 1 게이트 산화막으로서 상기 [비교예 2]의 조건과 동일한 조건으로 100Å두께의 HTO를 형성하고, 이어서 상기 형성된 제 1 게이트 산화막인 HTO위에 제 2 게이트 산화막으로서 통상의 석영반응관을 이용한 발열시스템에서 습식분위기로 100Å두께의 습식산화막을 형성한다.
제1a도 및 제1b도는 상기 비교예 1과 비교예 2 및 실시예에 의해 형성된 산화막들의 상온에서의 T.D.D.B특성을 평가하여 나타낸 그래프로서, 제1a도는 비교예 1의 건식산화막의 T.D.D.B특성을 나타내고, 제1b도는 비교예 2의 HTO의 T.D.D.B특성을 나타내며, 제1c도는 실시예의 HTO+습식산화막의 T.D.D.B특성을 나타낸다.
제1a도 내지 제1c도에서 알 수 있는 바와 같이 본 발명의 실시예에 의한 HTO+습식산화막의 T.D.D.B특성이 종래의 건식산화막 및 HTO의 T.D.D.B특성보다 우수하다.
다음에 제2a도 내지 제2b도는 상기 비교예1과 비교예2 및 실시예에 의해 형성된 산화막들의 I-V특성을 나타낸 것으로, 제2a도는 비교예1의 건식산화막의 I-V특성을 나타내고, 제2b도는 비교예2의 HTO의 I-V특성을 나타내며, 제2c도는 실시예의 HTO+습식산화막의 I-V특성을 각각 나타낸다. I+V 특성의 측정장비로는 HP4145B를 사용하였으며, 스위프모드(sweep mode)로 램프스텝 3V, 전류 10μA, 척(Chuck)의 온도 100℃, 측정사이즈 0.004㎠의 조건에서 측정하였다.
상기 제2a도 내지 제2c도에서 알 수 있는 바와 같이 본 발명의 실시예에 의한 HTO+습식산화막이 중래의 건식산화막 및 HTO보다 브레이크다운(Breakdown)되는 전압 및 전류특성이 우수하다.
제3a도 내지 제3b도는 상기 비교예1과 비교예2 및 실시예에 의해 형성된 산화막들의 SIMS(Secondary Ion Mass Spectroscopy)분석결과를 나타낸 것으로, 제3a도는 비교예1의 건식산화막의 SIMS분석결과를 나타내고, 제3b도는 비교예2의 HTO의 SIMS분석결과를 나타내며, 제3c도는 실시예의 HTO+습식산화막의 SIMS분석결과를 각각 나타낸다.
제3a도의 건식산화막의 경우는 Cl-이온의 분포가 산화막내에서 산화막과 실리콘기판의 경계쪽으로 갈수록 많이 존재함을 알 수 있고, 제3b도의 HTO의 경우는 산화막내에 Cl-이온의 분포가 산화막과 실리콘기판의 경계쪽으로 갈수록 그 양이 줄어드는 것을 알 수 있다.
그러나 제3c도의 본 발명의 실시예에 의한 산화막의 경우는 산화막내에 Cl-이온이 골고루 전면적으로 같은 양이 분포함을 알 수 있다.
이상에서 알 수 있는 바와 같이 제 1 게이트 산화막으로 100Å강도 두께의 HTO를 성장시키고 제 1 게이트 산화막상에 제 2 게이트 산화막으로 100Å성도 두께의 습식산화막을 성장시켜 형성한 산화막의 막질이 가장 좋은 특성을 나타낸다. 이는 실리콘기판 표면의 상태와 무관하게 성장시킬 수 있고 실리콘기판 표면의 미세한 피팅등을 완화시킬 수 있으며 막질이 균일한 HTO의 장점과 전기적특성이 우수한 습식산화막의 장점을 조합시켜 산화막을 형성함으로써 나타나는 특징이다.
본 발명에 의한 HTO와 습식산화막의 제 1 및 제 2 게이트 산화막으로 이루어진 산화막을 MOS소자의 얇은 게이트 산화막으로 사용할 경우의 T.D.D.B특성을 종래의 건식산화막 및 HTO와 비교하면 다음과 같다.
이상 상술한 바와 같이 본 발명에 의하면, 우수한 전기적 특성을 갖는 좋은 막질의 게이트 산화막을 형성할 수 있음에 따라 반도체소자에의 적용시 소자의 신뢰성향상을 도모할 수 있다.
이상 상술한 바와 같이 본 발명에 의하면, 우수한 전기적 특성을 갖는 좋은 막질의 게이트 산화막을 형성할 수 있음에 따라 반도체소자에의 적용시 소자의 신뢰성향상을 도모할 수 있다.
Claims (5)
- 반도체 기판 상에 저압 화학기상 증착방법을 사용하여 제 1 게이트 산화막으로 HTO(High Temperature Oxide)막을 형성하는 단계; 및 상기 제 1 게이트 산화막 상에 제 2 게이트 산화막으로 습식산화막을 형성하는 단게를 포함하는 것을 특징으로 하는 반도체 소자의 게이트 산화막 형성방법.
- 제1항에 있어서, 상기 제 1 게이트 산화막은 700℃∼850℃의 온도범위에서 형성하는 것을 특징으로 하는 반도체소자의 게이트 산화막 형성방법.
- 제2항에 있어서, 상기 제 1 게이트 산화막의 두께는 50Å∼200Å임을 특징으로 하는 반도체소자의 게이트 산화막 형성방법.
- 제1항에 있어서, 상기 제 2 게이트 산화막은 800℃∼900℃의 온도범위에서 발열시스템(Pyrogenic system)을 이용하여 형성하는 것을 특징으로 하는 반도체소자의 게이트 산화막 형성방법.
- 제4항에 있어서, 상기 제 2 게이트 산화막의 두께는 50Å∼200Å임을 특징으로 하는 반도체소자의 게이트 산화막 형성방법.
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JP5253241A JPH06204209A (ja) | 1992-10-12 | 1993-10-08 | 半導体素子の酸化膜形成方法 |
US08/338,816 US5470611A (en) | 1992-10-12 | 1994-11-10 | Method for forming an oxide film of a semiconductor |
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US5646074A (en) * | 1995-12-15 | 1997-07-08 | Mosel Vitelic, Inc. | Method of forming gate oxide for field effect transistor |
US6211098B1 (en) | 1999-02-18 | 2001-04-03 | Taiwan Semiconductor Manufacturing Company | Wet oxidation method for forming silicon oxide dielectric layer |
US6706577B1 (en) | 1999-04-26 | 2004-03-16 | Taiwan Semiconductor Manufacturing Company | Formation of dual gate oxide by two-step wet oxidation |
DE10050009A1 (de) * | 2000-10-10 | 2002-04-18 | Forschungszentrum Juelich Gmbh | Keramischer Werkstoff als Korrosionsschutz |
KR100780643B1 (ko) * | 2006-06-29 | 2007-11-29 | 주식회사 하이닉스반도체 | 반도체 소자의 소자 분리막 형성방법 |
CN112992672B (zh) * | 2019-12-16 | 2022-10-14 | 山东有研半导体材料有限公司 | 一种硅基二氧化硅背封薄膜的制备方法 |
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