CN1255739A - 形成具有多晶硅-硅化钛结构的栅极的方法 - Google Patents
形成具有多晶硅-硅化钛结构的栅极的方法 Download PDFInfo
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- 229910021341 titanium silicide Inorganic materials 0.000 title claims abstract description 32
- 238000000034 method Methods 0.000 title claims abstract description 30
- FVBUAEGBCNSCDD-UHFFFAOYSA-N silicide(4-) Chemical group [Si-4] FVBUAEGBCNSCDD-UHFFFAOYSA-N 0.000 title description 10
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 44
- 230000003647 oxidation Effects 0.000 claims abstract description 42
- 229910021420 polycrystalline silicon Inorganic materials 0.000 claims abstract description 25
- 229920005591 polysilicon Polymers 0.000 claims abstract description 25
- 239000004065 semiconductor Substances 0.000 claims abstract description 10
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- 229910008484 TiSi Inorganic materials 0.000 claims description 30
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- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 abstract description 2
- 229910052719 titanium Inorganic materials 0.000 abstract description 2
- 239000010936 titanium Substances 0.000 abstract description 2
- 238000001704 evaporation Methods 0.000 description 5
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Abstract
本发明提供了一种在栅极的再氧化工序中防止栅极异常氧化,同时,可以减小栅极电阻的多晶硅-硅化物结构的栅极形成方法。包括依次形成栅极氧化膜、多晶硅膜和硅化钛膜;在硅化钛膜上,按照栅极的形状,形成屏蔽绝缘膜。接着,对屏蔽绝缘膜的屏蔽层进行腐蚀,对硅化钛膜和多晶硅膜进行腐蚀,形成栅极。又利用再氧化工序,对基板进行氧化,在上述栅极的侧面和上述基板表面上,形成厚度均匀的氧化膜。
Description
本发明涉及半导体元件的制造方法,特别是涉及形成具有多晶硅-硅化钛结构的栅极的方法,在上述多晶硅-硅化钛结构中,硅化钛层形成在多晶硅层上。
一般MOS(金属氧化物半导体)晶体管的栅极是用掺杂的多晶硅膜形成的。然而,由于半导体器件的高度集成化,栅极的线宽以及其它图形都做得非常微小。最近,结构的微小化达到元件的线宽为0.15微米(μm)以下的程度。与此相适应,通常作为栅极材料使用的掺杂的多晶硅,由于其比电阻特性高,延迟时间长,因此,对于要求快速动作的元件,难以适用。这个问题,随着半导体器件的高度集成化成为一个深刻的问题。因此,对于1GDRAM以上的半导体元件,主要采用由多晶硅膜和硅化钛膜层叠结构组成的多晶硅-硅化钛结构的栅极。
图1A至图1E为说明先前的多晶硅-硅化钛结构的栅极形成方法的截面图。
参见图1A,在半导体基底11上,用热生长方式或蒸镀方式,形成栅极氧化膜12,在该栅极氧化膜12上,再形成掺杂的多晶硅膜13。其次,如图1B所示,在多晶硅膜13上,使用硅化钛靶(TiSix),采用物理气相沉积(PVD)法,蒸镀一层非晶体的硅化钛。(TiSix)膜14。然后,如图1C所示,在给定温度下,进行数秒钟的快速热处理(RTP),使非晶相的硅化钛膜14相变(phasetransformation)为晶相的硅化钛膜14a。
再参见图1D,为了进行通常的自调整接触(SAC:self-aligned contact)工序等后续工序,在TiSi2膜14a上,按照栅极的形状,形成一个屏蔽绝缘膜15。这里,屏蔽绝缘膜15是用氧化膜或氮化膜制成的。接着,对屏蔽绝缘膜15的屏蔽层进行腐蚀,并对TiSi2膜14a和多晶硅膜13进行腐蚀,形成栅极100。
再参见图1E,为了除去腐蚀造成的损伤,并提高栅极氧化膜12的可靠性,要利用再氧化工序,对图1D的结构进行氧化,在栅极100的侧面和基底11的表面上,形成氧化膜16。这里,再氧化工序一般是在800℃以上的温度下,通过热氧化工序进行的。
但是,在进行上述再氧化工序时,由于TiSi2膜14a的快速氧化,栅极100的硅化钛(TiSi2)膜14a的侧面会过度氧化;这样,形成栅极100的TiSi2膜14a的线宽减少,栅极100的形态变形,如图1E所示。由于这样,难以进行用以形成源极和漏极的注入杂质离子的工序,而且栅极100电阻增加,结果,使元件的可靠性降低。
因此,本发明的目的是要提供一种在栅极再氧化工序时,可防止栅极的异常氧化,同时可以减少栅极电阻的多晶硅-硅化钛结构(titanium polycidestructure)的栅极的形成方法。
为了达到本发明的上述目的,本发明在半导体基底上,依次形成栅极氧化膜,多晶硅膜和硅化钛膜;在上述TiSi2膜上,按照栅极的形状,形成屏蔽绝缘膜;以上述屏蔽绝缘膜作为蚀刻掩模,对上述TiSi2膜和多晶硅膜进行腐蚀,形成栅极;和利用再氧化工序,对上述基板进行氧化,在上述栅极的侧面和上述基板表面上,形成厚度均匀的氧化膜;上述再氧化工序,是在750℃以下的温度下,利用在干燥气氛下进行氧化的方法进行的。
另外,再氧化工序是在700℃~750℃的温度下进行的,氧化膜的膜厚为30埃~60埃,最好为50埃。
通过以下结合附图对优选实施例的详细描述,本发明的上述以及其它目的、特点会更明显。附图中:
图1A~图.1E为用于说明现有技术的多晶硅-硅化钛结构的栅极形成方法的截面图;
图2A~图2E为用于说明本发明实施例的多晶硅-硅化钛结构的栅极形成方法的截面图;
图3为表示多晶硅膜和硅化钛(TiSi2)膜的氧化速度与温度的倒数(1/T)的关系的图。
以下,根据附图来详细说明本发明的优选实施例。
图2A~图2E为用于说明根据本发明的实施例的多晶硅-硅化钛结构的栅极形成方法的截面图。
参见图2A,在半导体基底21上,用热成长方式或蒸镀方式形成栅极氧化膜22,在栅极氧化膜22上,再蒸镀形成掺杂的多晶硅膜23。其次,如图2B所示,在多晶硅膜23上,采用使用硅化钛(TiSix)靶的物理气相沉积(PVD)法,蒸镀形成非晶相的硅化钛(TiSix)膜24。接着,如图2C所示,在给定温度下,在数秒钟内进行快速热处理(RTP),将非晶体的TiSix膜24相变为晶相的硅化钛(TiSi2)膜24a。
再参见图2D,为了进行通常的自调整接触(SAC)工序等后续工序,在TiSi2膜24a上,按照栅极的形态,形成屏蔽绝缘膜25。这里,屏蔽绝缘膜25是由氧化膜或氮化膜或者氧化膜与氮化膜的复合膜形成的。其次,以屏蔽绝缘膜25作为蚀刻掩模,对TiSi2膜24a和多晶硅膜23进行腐蚀,形成栅极200。
又参见图2E,为了除去由蚀刻工艺造成的损伤,并恢复栅极氧化膜22的可靠性,通过再氧化工序,对图2D的结构再进行氧化,在栅极200的侧面和基底21的表面上形成氧化膜26。这里,为了使氧化膜26的厚度均匀,应在TiSi2膜24a和多晶硅膜23的氧化速度一致的温度范围内,进行再氧化工序。
例如,分别在700℃,750℃,800℃,850℃的温度下进行再氧化工序的实验结果显示,在800℃和850℃下,TiSi2膜24a的氧化速度比多晶硅膜23的氧化速度高。因此,如现有技术(参见图1E)那样,会发生TiSi2膜24a的侧面氧化过度的现象。另一方面,如图2E所示,在700℃和750℃下TiSi2膜24a和多晶硅膜23的氧化速度大致是一致的,因此,在栅极200的侧面上,可以形成厚度均匀的氧化膜26,如图2E所示。
图3为表示由上述实验得出的多晶硅膜23和TiSi2膜24a的氧化速度,与温度的倒数(1/T)的关系的图。如图3所示,当温度增加时,TiSi2膜的氧化速度也增加;而在750℃以下,多晶硅膜23和TiSi2膜24a的氧化速度大致是一致的。但是,在700℃以下,氧化速度太慢,工序时间长。因此,再氧化工序最好在700℃~750℃温度下进行。
另外,分别在700℃,750℃,800℃的温度下,利用在潮湿气氛下进行氧化的方法,进行再氧化工序的另一实验结果显示,在700℃和750℃下,在图2E所示的多晶硅膜23和TiSi2膜24a的侧面上,都能形成比较均匀的氧化膜26。相反,在800℃温度下,TiSi2膜24a的氧化速度快,因此,会发生如现有技术(参见图1E)那样的、TiSi2膜24a的侧面氧化过度的现象。但是,与在干燥气氛下进行的氧化比较,由于在潮湿气氛下进行氧化时的氧化均匀性差、氧化速度快,因此,再氧化工序最好采取在干燥的气氖下氧化的方法进行。
根据上述实验结果可知,再氧化工序最好是在700℃~750℃下,利用在干燥的气氛下进行氧化的方法进行,这样可形成厚度均匀的氧化膜26。另外,氧化膜26的膜厚为30(埃)~60埃,最好为50埃。
根据本发明,通过在TiSi2膜和多晶硅膜的氧化速度一致的温度范围内,利用在干燥气氛下进行氧化的方法进行再氧化工序,可以防止TiSi2膜的过度氧化。与此相适应,可以防止栅极的异常氧化,用于形成源极和漏极的注入杂质离子的工序容易进行,栅极电阻可以减小。结果,可以提高元件的可靠性。
本发明不是仅限于上述实施例。在不偏离本发明精神的范围内,可以作各种改变。
Claims (7)
1.一种形成具有多晶硅-硅化物结构的栅极的方法,该方法包括下列步骤:
在半导体基底上,依次形成栅极氧化膜,多晶硅膜和硅化钛膜;
在上述TiSi2膜上,按照栅极的形状,形成屏蔽绝缘膜;
以上述屏蔽绝缘膜作为蚀刻掩模,对上述TiSi2膜和多晶硅膜进行腐蚀,形成栅极;和
利用再氧化工序,对上述基板进行氧化,在上述栅极的侧面和上述基板表面上,形成厚度均匀的氧化膜;其特征为,上述再氧化工序,是在750℃以下的温度下,利用在干燥气氛下进行氧化的方法进行的。
2.如权利要求1所述的方法,其特征为,上述再氧化工序是在700℃~750℃温度下进行的。
3.如权利要求1所述的方法,其特征为,上述氧化膜的膜厚为30埃~60埃。
4.如权利要求3所述的方法,其特征为,上述氧化膜的膜厚大致为50埃。
5.如权利要求1所述的方法,其特征为,形成上述硅化钛膜的步骤包括:在上述多晶硅膜上,沉积一层非晶相的硅化钛膜的步骤;和对上述非晶相的硅化钛膜进行热处理,使该硅化钛膜相变为晶相的硅化钛膜的步骤。
6.如权利要求5所述的方法,其特征为,上述非晶相的硅化钛膜,是用物理气相沉积方式沉积形成的。
7.如权利要求5所述的方法,其特征为,上述热处理是利用快速热处理工序进行的。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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KR51104/1998 | 1998-11-26 | ||
KR1019980051104A KR100291512B1 (ko) | 1998-11-26 | 1998-11-26 | 반도체 소자의 게이트 전극 형성방법 |
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CN1255739A true CN1255739A (zh) | 2000-06-07 |
CN1161822C CN1161822C (zh) | 2004-08-11 |
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CNB991248996A Expired - Fee Related CN1161822C (zh) | 1998-11-26 | 1999-11-26 | 形成具有多晶硅-硅化钛结构的栅极的方法 |
Country Status (7)
Country | Link |
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US (1) | US6255206B1 (zh) |
JP (1) | JP3605718B2 (zh) |
KR (1) | KR100291512B1 (zh) |
CN (1) | CN1161822C (zh) |
DE (1) | DE19956987B4 (zh) |
GB (1) | GB2344216B (zh) |
TW (1) | TW425638B (zh) |
Cited By (1)
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CN100440441C (zh) * | 2005-06-30 | 2008-12-03 | 海力士半导体有限公司 | 用于制作具有栅的半导体器件的方法 |
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JP3875077B2 (ja) * | 2001-11-16 | 2007-01-31 | 富士通株式会社 | 電子デバイス及びデバイス接続方法 |
DE10214126A1 (de) * | 2002-03-28 | 2003-10-23 | Infineon Technologies Ag | Herstellungsverfahren für eine Mehrzahl von ungefähr gleich hohen und gleich beabstandeten Gatestapeln auf einem Halbleitersubstrat |
KR100486294B1 (ko) * | 2002-12-30 | 2005-04-29 | 삼성전자주식회사 | 게이트 패턴을 갖는 반도체소자의 제조방법 |
KR100460069B1 (ko) * | 2003-04-14 | 2004-12-04 | 주식회사 하이닉스반도체 | 반도체소자의 게이트전극 형성방법 |
TW200501317A (en) * | 2003-06-17 | 2005-01-01 | Promos Technologies Inc | Method of forming a contact hole and method of forming a semiconductor device |
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-
1998
- 1998-11-26 KR KR1019980051104A patent/KR100291512B1/ko not_active IP Right Cessation
-
1999
- 1999-11-04 TW TW088119190A patent/TW425638B/zh not_active IP Right Cessation
- 1999-11-05 US US09/434,647 patent/US6255206B1/en not_active Expired - Lifetime
- 1999-11-12 JP JP32298699A patent/JP3605718B2/ja not_active Expired - Fee Related
- 1999-11-18 GB GB9927341A patent/GB2344216B/en not_active Expired - Fee Related
- 1999-11-26 DE DE19956987A patent/DE19956987B4/de not_active Expired - Fee Related
- 1999-11-26 CN CNB991248996A patent/CN1161822C/zh not_active Expired - Fee Related
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Publication number | Priority date | Publication date | Assignee | Title |
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CN100440441C (zh) * | 2005-06-30 | 2008-12-03 | 海力士半导体有限公司 | 用于制作具有栅的半导体器件的方法 |
US7605069B2 (en) | 2005-06-30 | 2009-10-20 | Hynix Semiconductor Inc. | Method for fabricating semiconductor device with gate |
Also Published As
Publication number | Publication date |
---|---|
DE19956987B4 (de) | 2008-10-30 |
GB9927341D0 (en) | 2000-01-12 |
KR100291512B1 (ko) | 2001-11-05 |
GB2344216A (en) | 2000-05-31 |
JP3605718B2 (ja) | 2004-12-22 |
JP2000164871A (ja) | 2000-06-16 |
TW425638B (en) | 2001-03-11 |
GB2344216B (en) | 2003-09-24 |
CN1161822C (zh) | 2004-08-11 |
KR20000034009A (ko) | 2000-06-15 |
DE19956987A1 (de) | 2000-05-31 |
US6255206B1 (en) | 2001-07-03 |
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