TWI584475B - Process for forming repair layer and mos transistor having repair layer - Google Patents
Process for forming repair layer and mos transistor having repair layer Download PDFInfo
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- 238000000034 method Methods 0.000 title claims description 52
- 239000010410 layer Substances 0.000 claims description 89
- 125000006850 spacer group Chemical group 0.000 claims description 48
- 239000000463 material Substances 0.000 claims description 31
- 239000000758 substrate Substances 0.000 claims description 25
- 239000004020 conductor Substances 0.000 claims description 23
- 238000007254 oxidation reaction Methods 0.000 claims description 23
- 230000003647 oxidation Effects 0.000 claims description 22
- MZLGASXMSKOWSE-UHFFFAOYSA-N tantalum nitride Chemical compound [Ta]#N MZLGASXMSKOWSE-UHFFFAOYSA-N 0.000 claims description 17
- KZNMRPQBBZBTSW-UHFFFAOYSA-N [Au]=O Chemical compound [Au]=O KZNMRPQBBZBTSW-UHFFFAOYSA-N 0.000 claims description 11
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 11
- 239000002344 surface layer Substances 0.000 claims description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
- 229910052732 germanium Inorganic materials 0.000 claims description 7
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical group [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims description 7
- SIWVEOZUMHYXCS-UHFFFAOYSA-N oxo(oxoyttriooxy)yttrium Chemical compound O=[Y]O[Y]=O SIWVEOZUMHYXCS-UHFFFAOYSA-N 0.000 claims description 6
- 229910052735 hafnium Inorganic materials 0.000 claims description 5
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 5
- BPUBBGLMJRNUCC-UHFFFAOYSA-N oxygen(2-);tantalum(5+) Chemical group [O-2].[O-2].[O-2].[O-2].[O-2].[Ta+5].[Ta+5] BPUBBGLMJRNUCC-UHFFFAOYSA-N 0.000 claims description 5
- 229910001936 tantalum oxide Inorganic materials 0.000 claims description 5
- 229910001922 gold oxide Inorganic materials 0.000 claims description 4
- NFFIWVVINABMKP-UHFFFAOYSA-N methylidynetantalum Chemical compound [Ta]#C NFFIWVVINABMKP-UHFFFAOYSA-N 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical group [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 3
- 229910052707 ruthenium Inorganic materials 0.000 claims description 3
- 229910003468 tantalcarbide Inorganic materials 0.000 claims description 3
- GPMBECJIPQBCKI-UHFFFAOYSA-N germanium telluride Chemical compound [Te]=[Ge]=[Te] GPMBECJIPQBCKI-UHFFFAOYSA-N 0.000 claims description 2
- 238000005121 nitriding Methods 0.000 claims 3
- 230000006837 decompression Effects 0.000 claims 1
- 229910044991 metal oxide Inorganic materials 0.000 claims 1
- 150000004706 metal oxides Chemical class 0.000 claims 1
- 239000002356 single layer Substances 0.000 claims 1
- RUDFQVOCFDJEEF-UHFFFAOYSA-N yttrium(III) oxide Inorganic materials [O-2].[O-2].[O-2].[Y+3].[Y+3] RUDFQVOCFDJEEF-UHFFFAOYSA-N 0.000 claims 1
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 5
- 229920005591 polysilicon Polymers 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 4
- 229910000577 Silicon-germanium Inorganic materials 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 229910052727 yttrium Inorganic materials 0.000 description 3
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910001925 ruthenium oxide Inorganic materials 0.000 description 2
- WOCIAKWEIIZHES-UHFFFAOYSA-N ruthenium(iv) oxide Chemical compound O=[Ru]=O WOCIAKWEIIZHES-UHFFFAOYSA-N 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 239000013589 supplement Substances 0.000 description 2
- 229910052684 Cerium Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical group [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 description 1
- 229910000420 cerium oxide Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000010405 reoxidation reaction Methods 0.000 description 1
- 238000005549 size reduction Methods 0.000 description 1
- XSOKHXFFCGXDJZ-UHFFFAOYSA-N telluride(2-) Chemical compound [Te-2] XSOKHXFFCGXDJZ-UHFFFAOYSA-N 0.000 description 1
- 230000036962 time dependent Effects 0.000 description 1
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- Insulated Gate Type Field-Effect Transistor (AREA)
- Electrodes Of Semiconductors (AREA)
Description
本發明是有關於一種修補層的形成方法及具有修補層之金氧半電晶體結構,且特別是有關於一種在閘極結構側壁表面形成修補層之方法及閘極結構側壁具有修補層之金氧半電晶體結構。The present invention relates to a method for forming a repair layer and a gold oxide semi-transistor structure having a repair layer, and more particularly to a method for forming a repair layer on a sidewall surface of a gate structure and a gold layer having a repair layer on a sidewall of the gate structure Oxygen semi-transistor structure.
隨著元件積集度之要求增加,完成於半導體晶片上之電晶體元件必須越來越小,但是尺寸縮小將嚴重影響電晶體元件的性能,例如電晶體開啟狀態電流(Ion)變小與閘極漏電流(Jg)過大等缺失。因此,如何在有限尺寸的條件下,有效地增進電晶體元件的性能,便是發展本案之主要目的。As the component integration requirements increase, the transistor components completed on the semiconductor wafer must be smaller and smaller, but the size reduction will seriously affect the performance of the transistor component, such as the transistor on-state current (Ion) becomes smaller and the gate Missing leakage current (Jg) is too large. Therefore, how to effectively improve the performance of the transistor component under the condition of limited size is the main purpose of the development of the present case.
本發明提出一種修補層形成方法,此方法包含下列步驟。首先,提供基板,該基板上方已形成有閘極結構,該閘極結構至少包含有閘極介電層以及閘極導體結構。接著,執行氮化製程而在閘極結構表面上形成含氮表面層。接著,對含氮表面層進行熱氧化法以形成修補層。The present invention provides a method of forming a repair layer, the method comprising the following steps. First, a substrate is provided having a gate structure formed over the substrate, the gate structure including at least a gate dielectric layer and a gate conductor structure. Next, a nitridation process is performed to form a nitrogen-containing surface layer on the surface of the gate structure. Next, the nitrogen-containing surface layer is subjected to thermal oxidation to form a repair layer.
在本發明的較佳實施例中,上述基板之材料為矽,上述閘極介電層之材料為氧化矽、氮化矽或氮氧化矽,上述閘極導體結構之材料為多晶矽。In a preferred embodiment of the present invention, the material of the substrate is germanium, and the material of the gate dielectric layer is tantalum oxide, tantalum nitride or hafnium oxynitride, and the material of the gate conductor structure is polysilicon.
在本發明的較佳實施例中,上述氮化製程係為去耦合電漿氮化製程。In a preferred embodiment of the invention, the nitridation process is a decoupled plasma nitridation process.
在本發明的較佳實施例中,執行上述去耦合電漿氮化製程之壓力範圍為5毫托耳(mTorr)至15毫托耳(mTorr),能量範圍為1000瓦特(Watt)至2400瓦特(Watt),操作時間範圍為25秒至45秒。In a preferred embodiment of the invention, the decoupling plasma nitridation process is performed at a pressure in the range of 5 millitorr (mTorr) to 15 millitorr (mTorr) and an energy range of 1000 watts to 2400 watts. (Watt), operating time range is 25 seconds to 45 seconds.
在本發明的較佳實施例中,上述熱氧化法為濕式快速熱氧化法或乾式快速熱氧化法。In a preferred embodiment of the invention, the thermal oxidation process is a wet rapid thermal oxidation process or a dry rapid thermal oxidation process.
在本發明的較佳實施例中,上述熱氧化法之溫度範圍為800℃至900℃。In a preferred embodiment of the invention, the thermal oxidation process has a temperature in the range of from 800 °C to 900 °C.
在本發明的較佳實施例中,上述熱氧化法為爐管加熱氧化法。In a preferred embodiment of the invention, the thermal oxidation process is a furnace tube heating oxidation process.
在本發明的較佳實施例中,上述爐管加熱氧化法的溫度範圍為700℃至800℃。In a preferred embodiment of the invention, the furnace tube is heated to a temperature ranging from 700 ° C to 800 ° C.
在本發明的較佳實施例中,上述修補層的厚度範圍為10埃()至20埃()。In a preferred embodiment of the invention, the repair layer has a thickness in the range of 10 angstroms ( ) to 20 angstroms ( ).
在本發明之一實施例中,上述修補層為氮氧化矽層。In an embodiment of the invention, the repair layer is a ruthenium oxynitride layer.
在本發明的較佳實施例中,上述修補層形成方法更包含下列步驟:於修補層側壁表面形成第一間隙壁;於第一間隙壁表面形成犧牲間隙壁;以及於犧牲間隙壁表面形成第二間隙壁。In a preferred embodiment of the present invention, the repair layer forming method further comprises the steps of: forming a first spacer on the sidewall of the repair layer; forming a sacrificial spacer on the surface of the first spacer; and forming a surface on the surface of the sacrificial spacer Two gap walls.
在本發明之一實施例中,上述第一間隙壁之材料為厚度範圍為50埃()至100埃()之氮化矽,上述犧牲間隙壁之材料由厚度範圍為25埃()至75埃()之氧化矽及厚度範圍為200埃()至400埃()之氮化矽所組成及上述第二間隙壁之材料的總厚度範圍為200埃()至400埃()。In an embodiment of the invention, the material of the first spacer is a thickness of 50 angstroms ( ) to 100 angstroms ( The tantalum nitride, the material of the above-mentioned sacrificial spacer has a thickness ranging from 25 angstroms ( ) to 75 angstroms ( ) yttrium oxide and a thickness range of 200 angstroms ( ) to 400 angstroms ( The total thickness of the material of the tantalum nitride and the material of the second spacer is 200 angstroms ( ) to 400 angstroms ( ).
本發明亦提出一種金氧半電晶體結構,設置在基板上方,金氧半電晶體結構包含:閘極介電層,設置在基板上方;閘極導體結構,設置在閘極介電層上方;以及修補層,至少覆蓋在閘極導體結構之側壁表面,且其修補層為氮氧化矽層。The invention also provides a gold-oxygen semi-transistor structure, disposed above the substrate, the gold-oxygen semi-transistor structure comprises: a gate dielectric layer disposed above the substrate; and a gate conductor structure disposed above the gate dielectric layer; And the repair layer covers at least the sidewall surface of the gate conductor structure, and the repair layer is a layer of oxynitride.
在本發明之一實施例中,上述基板之材料為矽,上述閘極介電層之材料為氧化矽、氮化矽或氮氧化矽,上述閘極導體結構之材料為多晶矽。In an embodiment of the invention, the material of the substrate is germanium, and the material of the gate dielectric layer is tantalum oxide, tantalum nitride or hafnium oxynitride, and the material of the gate conductor structure is polysilicon.
在本發明之一實施例中,上述修補層的厚度範圍為10埃()至20埃()。In an embodiment of the invention, the repair layer has a thickness in the range of 10 angstroms ( ) to 20 angstroms ( ).
在本發明之一實施例中,上述氮氧化矽層中之氮混合比例範圍為5%至40%。In an embodiment of the invention, the nitrogen mixing ratio in the ruthenium oxynitride layer ranges from 5% to 40%.
在本發明之一實施例中,上述金氧半電晶體結構更包含第一間隙壁,形成於修補層側壁表面;輕摻雜汲極結構,形成於基板中,其位置與寬度相對應至第一間隙壁之位置與寬度;犧牲間隙壁,形成於第一間隙壁表面;以及第二間隙壁,形成於犧牲間隙壁表面。In an embodiment of the invention, the MOS semi-transistor structure further includes a first spacer formed on the sidewall of the repair layer; and a lightly doped 汲 structure formed in the substrate, the position and the width corresponding to the first a position and a width of the spacer; a sacrificial spacer formed on the first spacer surface; and a second spacer formed on the surface of the sacrificial spacer.
在本發明之一實施例中,上述第一間隙壁之材料為厚度範圍為50埃()至100埃()之氮化矽,上述犧牲間隙壁之材料由厚度範圍為25埃()至75埃()之氧化矽及厚度範圍為200埃()及400埃()之氮化矽所組成、上述第二間隙壁之材料的總厚度範圍為200埃()至400埃()。In an embodiment of the invention, the material of the first spacer is a thickness of 50 angstroms ( ) to 100 angstroms ( The tantalum nitride, the material of the above-mentioned sacrificial spacer has a thickness ranging from 25 angstroms ( ) to 75 angstroms ( ) yttrium oxide and a thickness range of 200 angstroms ( ) and 400 angstroms ( The composition of the tantalum nitride, the total thickness of the material of the second spacer is 200 angstroms ( ) to 400 angstroms ( ).
在本發明之一實施例中,上述金氧半電晶體結構更包含一源/汲極結構,形成於基板中,源/汲極結構之材料為矽化鍺(SiGe)或碳化矽(SiC)。In an embodiment of the invention, the MOS semi-transistor structure further comprises a source/drain structure formed in the substrate, and the material of the source/drain structure is bismuth telluride (SiGe) or tantalum carbide (SiC).
為讓本發明之上述和其他目的、特徵和優點能更明顯易懂,下文特舉較佳實施例,並配合所附圖式,作詳細說明如下。The above and other objects, features and advantages of the present invention will become more <RTIgt;
本發明在此所探討的技術手段為一種修補層之形成方法及具有修補層之金氧半電晶體結構。為了能徹底地瞭解本發明,將在下列的描述中以一種閘極結構為例進行說明。顯然地,本發明的實行並未限定以此種閘極結構之特殊細節,然而,對於本發明的較佳實施例,則會詳細描述如下。除了這些詳細描述之外,本發明還可以廣泛地施行在其他的實施例中,且本發明的範圍不受限定,在不脫離本發明之精神和範圍內,當可作些許之更動與潤飾,因此本發明之專利保護範圍須視本說明書所附之申請專利範圍所界定者為準。The technical means discussed herein are a method of forming a repair layer and a gold oxide semi-transistor structure having a repair layer. In order to fully understand the present invention, a gate structure will be described as an example in the following description. Obviously, the implementation of the present invention is not limited to the specific details of such a gate structure, however, for the preferred embodiment of the present invention, it will be described in detail below. The present invention may be widely practiced in other embodiments, and the scope of the present invention is not limited thereto, and may be modified and modified without departing from the spirit and scope of the invention. Therefore, the scope of patent protection of the present invention is defined by the scope of the claims appended hereto.
請參見圖1a,其係製作金氧半電晶體過程中的閘極結構之示意圖,主要表示出於矽基板1上形成閘極介電層100、閘極導體結構101以及硬罩幕層102所構成之閘極結構10,而其中閘極導體結構101大多以多晶矽來完成,硬罩幕層102則以氧化矽、氮化矽或氮氧化矽完成。Please refer to FIG. 1a, which is a schematic diagram of a gate structure during the fabrication of a MOS semiconductor, mainly showing the formation of a gate dielectric layer 100, a gate conductor structure 101, and a hard mask layer 102 on a germanium substrate 1. The gate structure 10 is constructed, wherein the gate conductor structure 101 is mostly completed by polysilicon, and the hard mask layer 102 is completed by tantalum oxide, tantalum nitride or hafnium oxynitride.
由於定義閘極導體結構101時會對多晶矽進行蝕刻,因此容易於側壁產生缺陷(defect),因此在進行後續輕摻雜汲極(Lightly Doped Drain,簡稱LDD)製程之前,可先利用爐管加熱氧化法(furnace oxidation)的方式來執行再氧化(Re-oxidation)製程,溫度約750℃的再氧化(Re-oxidation)製程用以於閘極導體結構101之側壁上形成如圖1b中所示,厚度範圍為10埃()至20埃()的氧化矽層1010,主要用以修補多晶矽表面的缺陷,並可防止在閘極介電層100與閘極導體結構101交界處之厚度變厚,進而使得元件的效能(performance)提升。Since the polysilicon is etched when the gate conductor structure 101 is defined, defects are easily generated on the sidewalls, so that the furnace tube can be used for heating before the subsequent Lightly Doped Drain (LDD) process. A reoxidation process is performed by means of a furnace oxidation method, and a re-oxidation process at a temperature of about 750 ° C is formed on the sidewall of the gate conductor structure 101 as shown in FIG. 1b. , thickness range of 10 angstroms ( ) to 20 angstroms ( The ruthenium oxide layer 1010 is mainly used to repair the defects of the surface of the polysilicon and to prevent the thickness at the interface between the gate dielectric layer 100 and the gate conductor structure 101 from becoming thick, thereby improving the performance of the device.
另外,為能讓元件的效能更佳,本案提出另一實施例,首先,如圖2a所示,對圖1a中所示之結構先進行去耦合電漿氮化製程,用以於構成閘極導體結構101之側壁及基板表面形成一層含氮表面層1011。在此實施例中,去耦合電漿氮化製程(Decoupled Plasma Nitridation,簡稱DPN)之壓力範圍為5毫托耳(mTorr)至15毫托耳(mTorr)、能量範圍為1000瓦特(Watt)至2400瓦特(Watt)、操作時間範圍為25秒至45秒,將氮原子植入閘極導體結構101之側壁,進而形成含氮表面層1011。在此實施例中,含氮表面層1011的厚度範圍為10埃()至20埃()。In addition, in order to make the performance of the component better, another embodiment is proposed in the present invention. First, as shown in FIG. 2a, the structure shown in FIG. 1a is first subjected to a decoupling plasma nitridation process for forming a gate. A sidewall of the conductor structure 101 and a surface of the substrate form a nitrogen-containing surface layer 1011. In this embodiment, the decoupled plasma Nitridation (DPN) has a pressure in the range of 5 mTorr to 15 mTorr and an energy range of 1000 watts (Watt) to 2400 Watt, operating time range of 25 seconds to 45 seconds, implants nitrogen atoms into the sidewalls of the gate conductor structure 101 to form a nitrogen-containing surface layer 1011. In this embodiment, the nitrogen-containing surface layer 1011 has a thickness in the range of 10 angstroms ( ) to 20 angstroms ( ).
接著,在已形成含氮表面層1011之閘極結構10上再執行熱氧化製程(thermal oxidation process),進而形成如圖2b所示之修補層1012,其材質主要為氮氧化矽,厚度範圍為10埃()至20埃(),較佳的厚度為15埃(),氮氧化矽層中之氮混合比例範圍為5%至40%。此氮氧化矽修補層1012,除了可修補閘極導體結構101之側壁的缺陷外,較上述氧化矽層1010更可提供電晶體通道所需的應力,並可因利用氮原子來補充多晶矽中摻質因擴散流失所造成閘極導體結構101之空乏(depletion)現象。又當閘極介電層100之材料是氮氧化矽層時,以氮氧化矽完成修補層1012更可補充閘極介電層100可能損失的氮原子,進而提昇閘極介電層100的介電係數,有效增進元件的效能,例如具有較佳的依時性介電崩潰特性(TDDB,time dependent dielectric breakdown)。而熱氧化製程可以是濕式快速熱氧化(RTO,rapid thermal oxidation)製程,其操作溫度範圍為800℃~900℃之間。在本發明的另一實施例中,其熱氧化製程也可以是操作溫度範圍為800℃~900℃之間之乾式快速熱氧化製程,或是爐管加熱氧化法,其操作溫度範圍為700℃至800℃。Next, a thermal oxidation process is performed on the gate structure 10 on which the nitrogen-containing surface layer 1011 has been formed, thereby forming a repair layer 1012 as shown in FIG. 2b, which is mainly made of barium oxynitride and has a thickness range of 10 angstroms ( ) to 20 angstroms ( ), preferably 15 angstroms thick ( The nitrogen mixing ratio in the cerium oxynitride layer ranges from 5% to 40%. The yttrium oxynitride repair layer 1012, in addition to repairing the defects of the sidewall of the gate conductor structure 101, provides the stress required for the transistor channel more than the above ruthenium oxide layer 1010, and can be supplemented by the use of nitrogen atoms to supplement polycrystalline germanium. The depletion of the gate conductor structure 101 caused by the loss of mass diffusion. When the material of the gate dielectric layer 100 is a yttrium oxynitride layer, the repair layer 1012 is further filled with yttrium oxynitride to supplement the nitrogen atoms that may be lost by the gate dielectric layer 100, thereby improving the dielectric layer of the gate dielectric layer 100. The electrical coefficient effectively enhances the performance of the component, for example, has a better time dependent dielectric breakdown (TDDB). The thermal oxidation process may be a rapid thermal oxidation (RTO) process with an operating temperature range of 800 ° C to 900 ° C. In another embodiment of the present invention, the thermal oxidation process may also be a dry rapid thermal oxidation process with an operating temperature range of 800 ° C to 900 ° C, or a furnace tube heating oxidation process with an operating temperature range of 700 ° C. Up to 800 ° C.
接著如圖2c所示,於該修補層1012側壁表面形成第一間隙壁12,並可利用第一間隙壁12及閘極結構10來於該基板1中定義出輕摻雜汲極結構13,輕摻雜汲極結構13之位置與寬度係相對應至該第一間隙壁12之位置與寬度。然後利用一遮罩層(圖未示),例如是氮化矽層,其厚度範圍為150埃()至250埃()以自我對準的蝕刻方式在基板1內形成凹槽,因此使得凹槽與第一間隙壁12有一約遮罩層厚度的間隔距離,接著一磊晶製程將矽化鍺(SiGe)或碳化矽(SiC)形成於凹槽內,且高於基板1之表面,來完成PMOS之或NMOS之源/汲極結構14,最後去除該遮罩層。接著,於第一間隙壁12之表面上形成犧牲間隙壁(dummy spacer)15及於犧牲間隙壁15之表面上形成第二間隙壁16。第一間隙壁12之材料為厚度範圍為50埃()至100埃()之氮化矽,犧牲間隙壁15係由厚度範圍為25埃()至75埃()的氧化矽及厚度範圍為200埃()至400埃()之氮化矽所組成之雙層結構,第二間隙壁16之材料的總厚度範圍為200埃()至400埃(),第二間隙壁16之材料可以是氧化矽與氮化矽所組成的雙層結構。另外,如圖所示,於矽化鍺(SiGe)或碳化矽(SiC)之表面上覆蓋有一層矽蓋層(Si Cap)140。Then, as shown in FIG. 2c, a first spacer 12 is formed on the sidewall of the repair layer 1012, and the first spacer 12 and the gate structure 10 are used to define the lightly doped gate structure 13 in the substrate 1. The position and width of the lightly doped gate structure 13 correspond to the position and width of the first spacer 12. A mask layer (not shown) is then utilized, such as a tantalum nitride layer, having a thickness in the range of 150 angstroms ( ) to 250 angstroms ( Forming a recess in the substrate 1 in a self-aligned etching manner, thereby causing the recess to have a spacing distance from the first spacer 12 about the thickness of the mask layer, followed by an epitaxial process of germanium telluride (SiGe) or tantalum carbide (SiC) is formed in the recess and above the surface of the substrate 1 to complete the PMOS or NMOS source/drain structure 14, and finally remove the mask layer. Next, a dummy spacer 15 is formed on the surface of the first spacer 12 and a second spacer 16 is formed on the surface of the sacrificial spacer 15. The material of the first spacer 12 is in the range of 50 angstroms ( ) to 100 angstroms ( The tantalum nitride, the sacrificial spacer 15 is comprised of a thickness range of 25 angstroms ( ) to 75 angstroms ( ) yttrium oxide and a thickness range of 200 angstroms ( ) to 400 angstroms ( a two-layer structure composed of tantalum nitride, the total thickness of the material of the second spacer 16 is 200 angstroms ( ) to 400 angstroms ( The material of the second spacer 16 may be a two-layer structure composed of yttrium oxide and tantalum nitride. Further, as shown, a surface of SiGe or SiC is covered with a cap layer 140 (Si Cap) 140.
雖然本發明已以較佳實施例揭露如上,然其並非用以限定本發明,任何熟習此技藝者,在不脫離本發明之精神和範圍內,當可作些許之更動與潤飾,因此本發明之保護範圍當視後附之申請專利範圍所界定者為準。While the present invention has been described in its preferred embodiments, the present invention is not intended to limit the invention, and the present invention may be modified and modified without departing from the spirit and scope of the invention. The scope of protection is subject to the definition of the scope of the patent application.
1...基板1. . . Substrate
10...閘極結構10. . . Gate structure
12...第一間隙壁12. . . First spacer
13...輕摻雜汲極結構13. . . Lightly doped 汲 structure
14...源/汲極結構14. . . Source/drain structure
15...犧牲間隙壁15. . . Sacrificial spacer
16...第二間隙壁16. . . Second spacer
100...閘極介電層100. . . Gate dielectric layer
101...閘極導體結構101. . . Gate conductor structure
102...硬罩幕層102. . . Hard mask layer
1010...氧化矽層1010. . . Cerium oxide layer
1011...含氮表面層1011. . . Nitrogen-containing surface layer
1012...修補層1012. . . Repair layer
140...矽蓋層140. . . Cover layer
圖1a:為製作金氧半電晶體過程中的閘極結構之示意圖。Figure 1a: Schematic diagram of the gate structure during the fabrication of a gold oxide semi-transistor.
圖1b:為形成氧化矽層以修補閘極導體結構之示意圖。Figure 1b: Schematic diagram of the formation of a yttrium oxide layer to repair the gate conductor structure.
圖2a:為形成含氮表面層於閘極導體結構側壁及基板表面之示意圖。Figure 2a is a schematic view showing the formation of a nitrogen-containing surface layer on the sidewalls of the gate conductor structure and the surface of the substrate.
圖2b:為將含氮表面層轉化為修補層之示意圖。Figure 2b: Schematic representation of the conversion of a nitrogen-containing surface layer to a repair layer.
圖2c:為形成輕摻雜汲極結構及源/汲極結構於基板中之示意圖。Figure 2c: Schematic representation of the formation of a lightly doped gate structure and a source/drain structure in a substrate.
1...基板1. . . Substrate
10...閘極結構10. . . Gate structure
100...閘極介電層100. . . Gate dielectric layer
101...閘極導體結構101. . . Gate conductor structure
102...硬罩幕層102. . . Hard mask layer
1012...修補層1012. . . Repair layer
Claims (18)
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Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5188978A (en) * | 1990-03-02 | 1993-02-23 | International Business Machines Corporation | Controlled silicon doping of III-V compounds by thermal oxidation of silicon capping layer |
| US20030134461A1 (en) * | 2002-01-14 | 2003-07-17 | Macronix International Co., Ltd. | Method for reducing oxidation encroachment of stacked gate layer |
| US20080124861A1 (en) * | 2006-11-06 | 2008-05-29 | Wenli Lin | Electron mobility enhancement for MOS devices with nitrided polysilicon re-oxidation |
| US20100087052A1 (en) * | 2008-10-08 | 2010-04-08 | Applied Materials, Inc. | Dopant activation anneal to achieve less dopant diffusion (better usj profile) and higher activation percentage |
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2011
- 2011-06-27 TW TW100122407A patent/TWI584475B/en active
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5188978A (en) * | 1990-03-02 | 1993-02-23 | International Business Machines Corporation | Controlled silicon doping of III-V compounds by thermal oxidation of silicon capping layer |
| US20030134461A1 (en) * | 2002-01-14 | 2003-07-17 | Macronix International Co., Ltd. | Method for reducing oxidation encroachment of stacked gate layer |
| US20080124861A1 (en) * | 2006-11-06 | 2008-05-29 | Wenli Lin | Electron mobility enhancement for MOS devices with nitrided polysilicon re-oxidation |
| US20100087052A1 (en) * | 2008-10-08 | 2010-04-08 | Applied Materials, Inc. | Dopant activation anneal to achieve less dopant diffusion (better usj profile) and higher activation percentage |
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