CN103377894B - Method for manufacturing metal silicide - Google Patents
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- CN103377894B CN103377894B CN201210118972.1A CN201210118972A CN103377894B CN 103377894 B CN103377894 B CN 103377894B CN 201210118972 A CN201210118972 A CN 201210118972A CN 103377894 B CN103377894 B CN 103377894B
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- 229910052751 metal Inorganic materials 0.000 title claims abstract description 127
- 239000002184 metal Substances 0.000 title claims abstract description 126
- 229910021332 silicide Inorganic materials 0.000 title claims abstract description 84
- FVBUAEGBCNSCDD-UHFFFAOYSA-N silicide(4-) Chemical compound [Si-4] FVBUAEGBCNSCDD-UHFFFAOYSA-N 0.000 title claims abstract description 84
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 25
- 238000000034 method Methods 0.000 title abstract description 25
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims abstract description 128
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 51
- 238000000137 annealing Methods 0.000 claims abstract description 32
- 239000000758 substrate Substances 0.000 claims abstract description 19
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 18
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000010703 silicon Substances 0.000 claims abstract description 12
- VLJQDHDVZJXNQL-UHFFFAOYSA-N 4-methyl-n-(oxomethylidene)benzenesulfonamide Chemical compound CC1=CC=C(S(=O)(=O)N=C=O)C=C1 VLJQDHDVZJXNQL-UHFFFAOYSA-N 0.000 claims description 4
- 229910019001 CoSi Inorganic materials 0.000 claims description 4
- 229910005883 NiSi Inorganic materials 0.000 claims description 4
- 229910021340 platinum monosilicide Inorganic materials 0.000 claims description 4
- 229910017709 Ni Co Inorganic materials 0.000 claims description 3
- 229910003267 Ni-Co Inorganic materials 0.000 claims description 3
- 229910003262 Ni‐Co Inorganic materials 0.000 claims description 3
- 229910052697 platinum Inorganic materials 0.000 claims description 3
- 239000004065 semiconductor Substances 0.000 abstract description 4
- 239000010408 film Substances 0.000 description 12
- 239000000463 material Substances 0.000 description 6
- -1 NiPt Inorganic materials 0.000 description 4
- 230000003071 parasitic effect Effects 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 238000004544 sputter deposition Methods 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- 229910001092 metal group alloy Inorganic materials 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229910052814 silicon oxide Inorganic materials 0.000 description 2
- 125000006850 spacer group Chemical group 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 229910003266 NiCo Inorganic materials 0.000 description 1
- 229910020684 PbZr Inorganic materials 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- 229910000577 Silicon-germanium Inorganic materials 0.000 description 1
- 229910010413 TiO 2 Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 229910003481 amorphous carbon Inorganic materials 0.000 description 1
- 229910021417 amorphous silicon Inorganic materials 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 229910052747 lanthanoid Inorganic materials 0.000 description 1
- 150000002602 lanthanoids Chemical class 0.000 description 1
- 238000004518 low pressure chemical vapour deposition Methods 0.000 description 1
- 238000002488 metal-organic chemical vapour deposition Methods 0.000 description 1
- 229910021424 microcrystalline silicon Inorganic materials 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 description 1
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 1
- 229920005591 polysilicon Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
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- Electrodes Of Semiconductors (AREA)
- Insulated Gate Type Field-Effect Transistor (AREA)
Abstract
本发明公开了一种金属硅化物制造方法,包括步骤:在含硅衬底上形成特征线条;在含硅衬底和特征线条上形成镍基金属层,其中镍基金属层的厚度大于由源漏结深确定的形成镍基金属硅化物所需的最小厚度;执行第一退火,使得镍基金属层与含硅衬底反应形成均匀厚度的第一镍基金属硅化物;去除未反应的金属后,执行第二退火,使得第一镍基金属硅化物转化为均匀厚度的第二镍基金属硅化物。依照本发明的半导体器件制造方法,通过提高金属薄层的厚度,利用金属硅化物自对准工艺并控制工艺参数,分两步退火形成了具有均匀厚度的金属硅化物,从而均匀地降低了源漏电阻,进一步提高了器件的性能。
The invention discloses a metal silicide manufacturing method, comprising the steps of: forming characteristic lines on a silicon-containing substrate; forming a nickel-based metal layer on the silicon-containing substrate and the characteristic lines, wherein the thickness of the nickel-based metal layer is greater than that obtained by the The minimum thickness required to form nickel-based metal silicide determined by the drain junction depth; perform a first anneal so that the nickel-based metal layer reacts with the silicon-containing substrate to form a uniform thickness of the first nickel-based metal silicide; remove unreacted metal Afterwards, a second annealing is performed, so that the first nickel-based metal silicide is transformed into a second nickel-based metal silicide with a uniform thickness. According to the semiconductor device manufacturing method of the present invention, by increasing the thickness of the metal thin layer, using the metal silicide self-alignment process and controlling the process parameters, a metal silicide with a uniform thickness is formed by annealing in two steps, thereby uniformly reducing the source leakage resistance, which further improves the performance of the device.
Description
技术领域 technical field
本发明涉及一种金属硅化物制造方法,特别是涉及一种能有效提高金属硅化物薄膜的薄膜均匀性的方法。The invention relates to a metal silicide manufacturing method, in particular to a method capable of effectively improving the film uniformity of the metal silicide film.
背景技术 Background technique
IC集成度不断增大需要器件尺寸持续按此例缩小,然而电器工作电压有时维持不变,使得实际MOS器件内电场强度不断增大。高电场带来一系列可靠性问题,使得器件性能退化。例如,MOSFET源漏区之间的寄生串联电阻会使得等效工作电压下降。特别地,当半导体器件例如MOSFET的物理栅长接近亚30nm时,源漏寄生电阻已超过沟道电阻成为整个器件等效电阻的重要组成部分。为此,需要在源漏区上和/或中采用金属硅化物来有效降低源漏接触电阻和寄生串联电阻,以此提高MOSFET的器件性能。The continuous increase of IC integration requires the continuous reduction of device size according to this example. However, the operating voltage of electrical appliances sometimes remains unchanged, so that the electric field strength in the actual MOS device continues to increase. The high electric field brings a series of reliability problems, which degrades the performance of the device. For example, parasitic series resistance between the source and drain regions of a MOSFET will cause the equivalent operating voltage to drop. In particular, when the physical gate length of a semiconductor device such as MOSFET is close to sub-30nm, the source-drain parasitic resistance exceeds the channel resistance and becomes an important part of the equivalent resistance of the entire device. Therefore, it is necessary to use metal silicide on and/or in the source and drain regions to effectively reduce the source and drain contact resistance and parasitic series resistance, thereby improving the device performance of the MOSFET.
图1A至1C所示为现有技术的硅化物自对准工艺步骤的剖视图。如图1A所示,在含Si的衬底1上依次形成由栅极绝缘层2、栅极导电层3构成的多个栅极堆叠结构,在每个栅极堆叠结构两侧形成栅极侧墙4,然后在整个结构上形成金属薄层5,其材质为Ni基金属,例如为Ni、NiPt、NiCo、NiPtCo等等。值得注意的是,由于形成金属薄层5的工艺通常是溅射,受限于工艺条件以及溅射原理,在相邻的栅极堆叠结构之间的较窄区域(图中虚线框所示)上,金属薄层5的厚度要小于在该区域之外的较宽区域上的厚度,也即在器件的窄线条和宽线条之间存在金属薄层5的厚度差。在亚32nmCMOS工艺节点以下,这种厚度差异越发明显,甚至有时候可能造成窄线条上金属薄层5的缺失、断裂。如图1B所示,在例如250~300℃的较低温度下执行第一快速退火,使得金属薄层5与衬底1中所含的Si反应形成富Ni相的镍基金属硅化物6,例如Ni2Si、Ni2PtSi、Ni2CoSi、Ni2PtCoSi。由于前述的金属薄层5的厚度差,使得窄线条上的富Ni相的镍基金属硅化物6的厚度减小,甚至可能完全缺失、断裂,也即在该区域上没有形成富Ni相的镍基金属硅化物6。如图1C所示,剥除未反应的金属薄层5之后,在例如450~500℃的较高温度下执行第二快速退火,使得富Ni相的镍基金属硅化物6转化为具有较低电阻的镍基金属硅化物7,例如NiSi、NiPtSi、NiCoSi、NiPtCoSi。由于上述厚度差,使得最终形成的镍基金属硅化物7在窄线条和宽线条上的厚度也不均匀,即密集的栅极堆叠线条之间的部分上厚度明显较小,而其他较宽部分上厚度明显较大。线条越密集越窄,该区域上的金属硅化物薄膜厚度就越薄,电阻越大。然而在不同裸片管芯或者晶片的不同区域上,窄线条通常伴随着宽线条,因此金属硅化物薄膜厚度分布是不均匀的。这种厚度的不均匀性将引起器件接触、寄生电阻的不一致,导致器件电学性能发生不期望的改变。1A to 1C are cross-sectional views of the prior art silicide self-alignment process steps. As shown in FIG. 1A, a plurality of gate stack structures composed of a gate insulating layer 2 and a gate conductive layer 3 are sequentially formed on a substrate 1 containing Si, and gate sides are formed on both sides of each gate stack structure. wall 4, and then form a thin metal layer 5 on the entire structure, the material of which is Ni-based metal, such as Ni, NiPt, NiCo, NiPtCo and so on. It is worth noting that since the process of forming the thin metal layer 5 is usually sputtering, limited by the process conditions and the principle of sputtering, the narrow area between adjacent gate stack structures (shown by the dotted line box in the figure) Above, the thickness of the metal thin layer 5 is smaller than the thickness of the wider area outside this area, that is, there is a thickness difference of the metal thin layer 5 between the narrow line and the wide line of the device. Below the sub-32nm CMOS process node, this difference in thickness becomes more obvious, and sometimes may even cause missing and breaking of the thin metal layer 5 on the narrow lines. As shown in FIG. 1B, the first rapid annealing is performed at a lower temperature such as 250-300° C., so that the thin metal layer 5 reacts with the Si contained in the substrate 1 to form a nickel-based metal silicide 6 in a Ni-rich phase, For example Ni 2 Si, Ni 2 PtSi, Ni 2 CoSi, Ni 2 PtCoSi. Due to the thickness difference of the aforementioned metal thin layer 5, the thickness of the Ni-rich phase nickel-based metal silicide 6 on the narrow line is reduced, and may even be completely missing or fractured, that is, no Ni-rich phase is formed in this region. Nickel-based metal silicide 6. As shown in Figure 1C, after stripping off the unreacted metal thin layer 5, the second rapid annealing is performed at a higher temperature such as 450-500° C., so that the nickel-based metal silicide 6 of the Ni-rich phase is transformed into a Resistive nickel-based metal silicide 7, such as NiSi, NiPtSi, NiCoSi, NiPtCoSi. Due to the above-mentioned difference in thickness, the thickness of the finally formed nickel-based metal silicide 7 on narrow lines and wide lines is not uniform, that is, the thickness of the part between the dense gate stack lines is obviously smaller, while other wider parts The upper thickness is significantly larger. The denser and narrower the lines, the thinner the metal silicide film thickness on this area, and the greater the resistance. However, on different dies or different regions of the wafer, narrow lines are usually accompanied by wide lines, so the metal silicide film thickness distribution is not uniform. Such thickness inhomogeneity will cause inconsistencies in device contact and parasitic resistance, resulting in undesired changes in the electrical properties of the device.
由此可见,现有的金属硅化物工艺使得薄膜厚度不均匀,降低了器件的电学性能和可靠性。It can be seen that the existing metal silicide process makes the thickness of the film uneven, which reduces the electrical performance and reliability of the device.
发明内容 Contents of the invention
由上所述,本发明的目的在于提供一种能有效提高金属硅化物薄膜厚度均匀性的半导体器件制造方法。From the above, the purpose of the present invention is to provide a semiconductor device manufacturing method that can effectively improve the thickness uniformity of the metal silicide film.
为此,本发明提供了一种金属硅化物制造方法,包括步骤:在含硅衬底上形成特征线条;在含硅衬底和特征线条上形成镍基金属层,其中镍基金属层的厚度大于由源漏结深确定的形成镍基金属硅化物所需的最小厚度;执行第一退火,使得镍基金属层与含硅衬底反应形成均匀厚度的第一镍基金属硅化物;去除未反应的金属后,执行第二退火,使得第一镍基金属硅化物转化为均匀厚度的第二镍基金属硅化物。For this reason, the present invention provides a kind of metal silicide manufacturing method, comprises the steps: form characteristic line on silicon-containing substrate; Form nickel-based metal layer on silicon-containing substrate and characteristic line, wherein the thickness of nickel-based metal layer greater than the minimum thickness required to form the nickel-based metal silicide determined by the depth of the source-drain junction; perform the first annealing, so that the nickel-based metal layer reacts with the silicon-containing substrate to form a first nickel-based metal silicide with a uniform thickness; After reacting the metal, a second anneal is performed so that the first Ni-based metal silicide is converted into a second Ni-based metal silicide with a uniform thickness.
其中,镍基金属层的厚度为7~200nm 。Wherein, the thickness of the nickel-based metal layer is 7-200nm.
其中,镍基金属层包括Ni、Ni-Pt、Ni-Co、Ni-Pt-Co。其中,非Ni金属的含量为1%~50%。Wherein, the nickel-based metal layer includes Ni, Ni-Pt, Ni-Co, Ni-Pt-Co. Wherein, the content of non-Ni metal is 1%-50%.
其中,第二退火的温度高于第一退火的温度。其中,第一退火温度为150~300℃,第二退火温度为450~550℃。Wherein, the temperature of the second annealing is higher than the temperature of the first annealing. Wherein, the first annealing temperature is 150-300°C, and the second annealing temperature is 450-550°C.
其中,第一镍基金属硅化物中的Ni含量大于第二镍基金属硅化物中的Ni含量。其中,第一镍基金属硅化物包括Ni2Si、Ni2PtSi、Ni2CoSi、Ni2PtCoSi,第二镍基金属硅化物包括NiSi、NiPtSi、NiCoSi、NiPtCoSi。Wherein, the Ni content in the first nickel-based metal silicide is greater than the Ni content in the second nickel-based metal silicide. Wherein, the first nickel-based metal silicide includes Ni 2 Si, Ni 2 PtSi, Ni 2 CoSi, Ni 2 PtCoSi, and the second nickel-based metal silicide includes NiSi, NiPtSi, NiCoSi, NiPtCoSi.
依照本发明的金属硅化物制造方法,通过提高金属薄层的厚度,利用金属硅化物自对准工艺并控制工艺参数,分两步退火形成了具有均匀厚度的金属硅化物,从而均匀地降低了源漏电阻,进一步提高了器件的性能。According to the metal silicide manufacturing method of the present invention, by increasing the thickness of the metal thin layer, using the metal silicide self-alignment process and controlling the process parameters, a metal silicide with a uniform thickness is formed by annealing in two steps, thereby uniformly reducing The source-drain resistance further improves the performance of the device.
附图说明 Description of drawings
以下参照附图来详细说明本发明的技术方案,其中:Describe technical scheme of the present invention in detail below with reference to accompanying drawing, wherein:
图1A至1C为现有技术的金属硅化物制造方法的剖面示意图;以及1A to 1C are schematic cross-sectional views of a metal silicide manufacturing method in the prior art; and
图2至图4为依照本发明的可有效提高薄膜均匀性的金属硅化物制造方法的各个步骤的剖面示意图。2 to 4 are schematic cross-sectional views of various steps of the metal silicide manufacturing method that can effectively improve the uniformity of the film according to the present invention.
具体实施方式 detailed description
以下参照附图并结合示意性的实施例来详细说明本发明技术方案的特征及其技术效果,公开了可有效提高薄膜均匀性的金属硅化物制造方法。需要指出的是,类似的附图标记表示类似的结构,本申请中所用的术语“第一”、“第二”、“上”、“下”等等可用于修饰各种器件结构或制造工序。这些修饰除非特别说明并非暗示所修饰器件结构或制造工序的空间、次序或层级关系。The features and technical effects of the technical solution of the present invention will be described in detail below with reference to the accompanying drawings and in combination with schematic embodiments, and a metal silicide manufacturing method that can effectively improve the uniformity of the film is disclosed. It should be pointed out that similar reference numerals represent similar structures, and the terms "first", "second", "upper", "lower" and the like used in this application can be used to modify various device structures or manufacturing processes . These modifications do not imply spatial, sequential or hierarchical relationships of the modified device structures or fabrication processes unless specifically stated.
图2至图4为依照本发明的可有效提高薄膜均匀性的金属硅化物制造方法的各个步骤的剖面示意图。2 to 4 are schematic cross-sectional views of various steps of the metal silicide manufacturing method that can effectively improve the uniformity of the film according to the present invention.
参照附图2,形成基础结构。如图2所示为基础结构的剖面示意图。With reference to accompanying drawing 2, form basic structure. Figure 2 is a schematic cross-sectional view of the basic structure.
首先提供衬底1,衬底1至少包含Si元素,例如体Si、绝缘体上Si(SOI)、SiGe、SiC等等,优选地衬底1为体Si或SOI。Firstly, a substrate 1 is provided, and the substrate 1 contains at least Si element, such as bulk Si, Si on insulator (SOI), SiGe, SiC, etc., preferably, the substrate 1 is bulk Si or SOI.
其次,在衬底1上形成多个特征线条。对于MOSFET制作而言,也即在衬底1上采用LPCVD、PECVD、HDPCVD、MOCVD、MBE等常规方法沉积依次沉积栅极绝缘层2、栅极导电层3,并刻蚀形成多个栅极堆叠结构。对于前栅工艺而言,栅极堆叠结构形成之后不再去除,作为最终的栅极堆叠,因此栅极绝缘层2为氧化硅、氮氧化硅或高k材料,高k材料包括但不限于氮化物(例如SiN、AIN、TiN)、金属氧化物(主要为副族和镧系金属元素氧化物,例如Al2O3、Ta2O5、TiO2、ZnO、ZrO2、HfO2、CeO2、Y2O3)、钙钛矿相氧化物(例如PbZrxTi1-xO3(PZT)、BaxSr1-xTiO3(BST));相应地,栅极导电层3为掺杂多晶硅、金属、金属合金、金属氮化物,其中所述金属包括W、Cu、Mo、Ti、Al、Ta等及其组合。对于后栅工艺而言,栅极堆叠为伪栅极堆叠,在稍后的工艺中将去除而形成栅极沟槽,以供后期重新填充形成栅极,因此栅极绝缘层2为氧化硅、氮氧化硅,栅极导电层3为多晶硅、微晶硅、非晶硅。在栅极堆叠结构2、3上沉积绝缘介质并刻蚀形成栅极侧墙4,其材质例如为氮化硅、氮氧化硅、类金刚石无定形碳(DLC)、金属氧化物(优选为具有高应力,例如大于1GPa,以向沟道施加应力提高驱动能力)。对于其他器件结构而言,特征线条可以为鳍形结构的Si线、密集的SRAM单元图形等等。Second, a plurality of feature lines are formed on the substrate 1 . For MOSFET fabrication, the gate insulating layer 2 and the gate conductive layer 3 are sequentially deposited on the substrate 1 by conventional methods such as LPCVD, PECVD, HDPCVD, MOCVD, and MBE, and etched to form multiple gate stacks. structure. For the front-gate process, the gate stack structure is not removed after formation, as the final gate stack, so the gate insulating layer 2 is silicon oxide, silicon oxynitride or a high-k material, and the high-k material includes but not limited to nitrogen Compounds (such as SiN, AIN, TiN), metal oxides (mainly subgroup and lanthanide metal element oxides, such as Al 2 O 3 , Ta 2 O 5 , TiO 2 , ZnO, ZrO 2 , HfO 2 , CeO 2 , Y 2 O 3 ), perovskite phase oxides (such as PbZr x Ti 1-x O 3 (PZT), Ba x Sr 1-x TiO 3 (BST)); correspondingly, the gate conductive layer 3 is doped Heteropolysilicon, metal, metal alloy, metal nitride, wherein the metal includes W, Cu, Mo, Ti, Al, Ta, etc. and combinations thereof. For the gate-last process, the gate stack is a dummy gate stack, which will be removed in a later process to form a gate trench for later refilling to form a gate, so the gate insulating layer 2 is silicon oxide, Silicon oxynitride, the gate conductive layer 3 is polysilicon, microcrystalline silicon, or amorphous silicon. An insulating medium is deposited on the gate stack structures 2 and 3 and etched to form a gate spacer 4, the material of which is, for example, silicon nitride, silicon oxynitride, diamond-like amorphous carbon (DLC), metal oxide (preferably with High stress, such as greater than 1 GPa, to apply stress to the channel to improve driving capability). For other device structures, the characteristic lines may be Si lines of fin-shaped structures, dense SRAM cell patterns, and the like.
然后,在整个器件上,也即在衬底1、以及由栅极侧墙4和栅极导电层3构成的特征线条上通过例如溅射的方法沉积金属层5,用作形成金属硅化物的前驱物。金属层5的厚度H 1足够厚,超过附图1中现有技术中采用金属硅化物自对准工艺形成金属硅化物所需的厚度H0(图2中虚线水平线所示)。H0通常取决于源漏结深(也即对于给定的未来形成金属硅化物之后源漏结深,所需的金属层5的最小厚度),例如为1~5nm;而H1例如大于等于1.4倍H0,例如为7~200nm 。金属层5的材质为镍基金属,也即至少包含Ni的金属或金属合金,例如为Ni、Ni-Pt、Ni-Co、Ni-Pt-Co,其中非Ni金属元素(Pt和/或Co)的总含量(原子数此)优选为1%~50%,也即相应的Ni含量为较高的50%~99%。Then, deposit a metal layer 5 on the entire device, that is, on the substrate 1 and the feature lines formed by the gate spacer 4 and the gate conductive layer 3 by, for example, sputtering to form a metal silicide Precursor. The thickness H1 of the metal layer 5 is thick enough to exceed the thickness H0 required to form the metal silicide by using the metal silicide self-alignment process in the prior art in FIG. 1 (indicated by the dotted horizontal line in FIG. 2 ). H0 usually depends on the depth of the source-drain junction (that is, the minimum thickness of the metal layer 5 required for a given depth of the source-drain junction after the metal silicide is formed in the future), for example, 1 to 5 nm; and H1, for example, is greater than or equal to 1.4 times H0 is, for example, 7 to 200 nm. The material of the metal layer 5 is a nickel-based metal, that is, a metal or a metal alloy containing at least Ni, such as Ni, Ni-Pt, Ni-Co, Ni-Pt-Co, wherein non-Ni metal elements (Pt and/or Co ) The total content (number of atoms) is preferably 1% to 50%, that is, the corresponding Ni content is relatively high 50% to 99%.
参照图3,执行第一退火,使得金属层5的金属与衬底1中的Si反应形成第一金属硅化物6,也即具有较高电阻的富金属相硅化物6。例如采用快速退火工艺,退火温度为较低的第一退火温度,为150~300℃,退火时间为5秒至5分钟。形成的富金属相硅化物6为富镍相硅化物,例如为Ni2Si、Ni2PtSi、Ni2CoSi、Ni2PtCoSi。在该较低的第一退火温度下,金属层5中富含的Ni原子扩散受限并且自饱和,因此富镍相硅化物6生长不会太厚,消耗完厚度为上述H0的Ni基金属层5之后就停止继续反应,因此富镍相硅化物6的厚度H2在衬底表面之上的那部分H2’等于或接近上述由源漏结深确定的金属硅化物工艺所需的金属层厚度H0,例如为1.0~1.1倍H0(虽然图3中显示为相等,但是实际上可以上下浮动)。富镍相硅化物6的厚度受限于退火温度、时间且硅化过程是自饱和的,而不再受限于金属层5的厚度(因为金属层5的厚度H1大于所需的厚度H0),因此富镍相硅化物6在整个晶片上具有相等的、均匀的厚度H2,由此可以保证后续形成低阻金属硅化物时薄膜的均匀性。Referring to FIG. 3 , the first annealing is performed so that the metal of the metal layer 5 reacts with the Si in the substrate 1 to form a first metal silicide 6 , that is, a metal-rich phase silicide 6 with higher resistance. For example, if the rapid annealing process is adopted, the annealing temperature is the lower first annealing temperature, which is 150-300° C., and the annealing time is 5 seconds to 5 minutes. The formed metal-rich silicide 6 is nickel-rich silicide, such as Ni 2 Si, Ni 2 PtSi, Ni 2 CoSi, Ni 2 PtCoSi. At this lower first annealing temperature, the diffusion of Ni atoms rich in the metal layer 5 is limited and self-saturated, so the nickel-rich phase silicide 6 will not grow too thick, and the Ni-based metal with the thickness above H0 will be consumed After the layer 5, the reaction is stopped, so the thickness H2 of the nickel-rich phase silicide 6 is above the substrate surface, and the part H2' is equal to or close to the metal layer thickness required by the metal silicide process determined by the depth of the source-drain junction. H0 is, for example, 1.0 to 1.1 times H0 (although it is shown as equal in FIG. 3 , it can actually fluctuate up and down). The thickness of the nickel-rich phase silicide 6 is limited by the annealing temperature and time, and the silicide process is self-saturated, and is no longer limited by the thickness of the metal layer 5 (because the thickness H1 of the metal layer 5 is greater than the required thickness H0), Therefore, the nickel-rich phase silicide 6 has an equal and uniform thickness H2 on the entire wafer, thereby ensuring the uniformity of the film when the low-resistance metal silicide is subsequently formed.
参照图4,去除未反应的金属后,执行第二退火,使得第一金属硅化物6转化为第二金属硅化物7,也即具有较低电阻的金属硅化物7。剥除图3中未反应的金属层5,也即厚度超过H0的那部分(其厚度为H1-H0)。采用快速退火工艺,退火温度为较高的第二退火温度(也即第二退火温度高于第一退火温度),为450~550℃,退火时间为5秒至3分钟。金属硅化物7为镍基金属硅化物,第二金属硅化物7中Ni含量低于第一金属硅化物6中的Ni含量。具体地,金属硅化物7例如为NiSi、NiPtSi、NiCoSi、NiPtCoSi 。由于图3中第一金属硅化物6形成过程是自饱和的且形成了厚度均匀的薄膜,因此图4中第二金属硅化物7的厚度也相应保持了均匀性,也即具有相同的厚度H3。依照退火温度和时间的不同,H3可以大于等于H2,例如为1.1~1.2倍H2。Referring to FIG. 4 , after removing the unreacted metal, a second annealing is performed so that the first metal silicide 6 is transformed into a second metal silicide 7 , that is, a metal silicide 7 with lower resistance. The unreacted metal layer 5 in FIG. 3 is peeled off, that is, the part whose thickness exceeds H0 (its thickness is H1-H0). The rapid annealing process is adopted, the annealing temperature is a higher second annealing temperature (that is, the second annealing temperature is higher than the first annealing temperature), which is 450-550° C., and the annealing time is 5 seconds to 3 minutes. The metal silicide 7 is a nickel-based metal silicide, and the Ni content in the second metal silicide 7 is lower than that in the first metal silicide 6 . Specifically, the metal silicide 7 is, for example, NiSi, NiPtSi, NiCoSi, NiPtCoSi. Since the formation process of the first metal silicide 6 in FIG. 3 is self-saturated and forms a thin film with uniform thickness, the thickness of the second metal silicide 7 in FIG. 4 also maintains uniformity correspondingly, that is, it has the same thickness H3 . Depending on the annealing temperature and time, H3 may be greater than or equal to H2, for example, 1.1-1.2 times H2.
由图4可见,最终形成的低阻Ni基金属硅化物7具有统一的薄膜厚度,因此也具有相同的薄膜电阻,提高了器件的均匀性和可靠性。It can be seen from FIG. 4 that the finally formed low-resistance Ni-based metal silicide 7 has a uniform film thickness, so it also has the same film resistance, which improves the uniformity and reliability of the device.
依照本发明的半导体器件制造方法,通过提高金属薄层的厚度,利用金属硅化物自对准工艺并控制工艺参数,分两步退火形成了具有均匀厚度的金属硅化物,从而均匀地降低了源漏电阻,进一步提高了器件的性能。According to the semiconductor device manufacturing method of the present invention, by increasing the thickness of the metal thin layer, using the metal silicide self-alignment process and controlling the process parameters, a metal silicide with a uniform thickness is formed by annealing in two steps, thereby uniformly reducing the source Leakage resistance, which further improves the performance of the device.
尽管已参照一个或多个示例性实施例说明本发明,本领域技术人员可以知晓无需脱离本发明范围而对器件结构做出各种合适的改变和等价方式。此外,由所公开的教导可做出许多可能适于特定情形或材料的修改而不脱离本发明范围。因此,本发明的目的不在于限定在作为用于实现本发明的最佳实施方式而公开的特定实施例,而所公开的器件结构及其制造方法将包括落入本发明范围内的所有实施例。While the invention has been described with reference to one or more exemplary embodiments, those skilled in the art will recognize various suitable changes and equivalents in device structures that do not depart from the scope of the invention. In addition, many modifications, possibly suited to a particular situation or material, may be made from the disclosed teaching without departing from the scope of the invention. Therefore, it is intended that the invention not be limited to the particular embodiment disclosed as the best mode for carrying out this invention, but that the disclosed device structures and methods of making the same will include all embodiments falling within the scope of the invention .
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