WO2018186248A1 - エピタキシャルシリコンウェーハの製造方法およびエピタキシャルシリコンウェーハ - Google Patents
エピタキシャルシリコンウェーハの製造方法およびエピタキシャルシリコンウェーハ Download PDFInfo
- Publication number
- WO2018186248A1 WO2018186248A1 PCT/JP2018/012640 JP2018012640W WO2018186248A1 WO 2018186248 A1 WO2018186248 A1 WO 2018186248A1 JP 2018012640 W JP2018012640 W JP 2018012640W WO 2018186248 A1 WO2018186248 A1 WO 2018186248A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- silicon wafer
- epitaxial
- epitaxial film
- plane
- less
- 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.)
- Ceased
Links
Images
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
- H10P14/20—Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials
- H10P14/34—Deposited materials, e.g. layers
- H10P14/3402—Deposited materials, e.g. layers characterised by the chemical composition
- H10P14/3404—Deposited materials, e.g. layers characterised by the chemical composition being Group IVA materials
- H10P14/3411—Silicon, silicon germanium or germanium
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/02—Pretreatment of the material to be coated
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/22—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
- C23C16/24—Deposition of silicon only
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B25/00—Single-crystal growth by chemical reaction of reactive gases, e.g. chemical vapour-deposition growth
- C30B25/02—Epitaxial-layer growth
- C30B25/18—Epitaxial-layer growth characterised by the substrate
- C30B25/20—Epitaxial-layer growth characterised by the substrate the substrate being of the same materials as the epitaxial layer
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B29/00—Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
- C30B29/02—Elements
- C30B29/06—Silicon
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B30/00—Production of single crystals or homogeneous polycrystalline material with defined structure characterised by the action of electric or magnetic fields, wave energy or other specific physical conditions
- C30B30/02—Production of single crystals or homogeneous polycrystalline material with defined structure characterised by the action of electric or magnetic fields, wave energy or other specific physical conditions using electric fields, e.g. electrolysis
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B30/00—Production of single crystals or homogeneous polycrystalline material with defined structure characterised by the action of electric or magnetic fields, wave energy or other specific physical conditions
- C30B30/08—Production of single crystals or homogeneous polycrystalline material with defined structure characterised by the action of electric or magnetic fields, wave energy or other specific physical conditions in conditions of zero-gravity or low gravity
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
- H10P14/20—Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials
- H10P14/24—Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials using chemical vapour deposition [CVD]
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
- H10P14/20—Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials
- H10P14/29—Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials characterised by the substrates
- H10P14/2901—Materials
- H10P14/2902—Materials being Group IVA materials
- H10P14/2905—Silicon, silicon germanium or germanium
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
- H10P14/20—Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials
- H10P14/29—Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials characterised by the substrates
- H10P14/2926—Crystal orientations
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
- H10P14/20—Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials
- H10P14/34—Deposited materials, e.g. layers
- H10P14/3438—Doping during depositing
- H10P14/3441—Conductivity type
- H10P14/3442—N-type
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
- H10P14/20—Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials
- H10P14/36—Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials characterised by treatments done before the formation of the materials
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
- H10P14/60—Formation of materials, e.g. in the shape of layers or pillars of insulating materials
- H10P14/63—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the formation processes
- H10P14/6326—Deposition processes
- H10P14/6349—Deposition of epitaxial materials
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
- H10P14/60—Formation of materials, e.g. in the shape of layers or pillars of insulating materials
- H10P14/69—Inorganic materials
- H10P14/6903—Inorganic materials containing silicon
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P90/00—Preparation of wafers not covered by a single main group of this subclass, e.g. wafer reinforcement
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P95/00—Generic processes or apparatus for manufacture or treatments not covered by the other groups of this subclass
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P95/00—Generic processes or apparatus for manufacture or treatments not covered by the other groups of this subclass
- H10P95/90—Thermal treatments, e.g. annealing or sintering
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P50/00—Etching of wafers, substrates or parts of devices
- H10P50/60—Wet etching
- H10P50/64—Wet etching of semiconductor materials
- H10P50/642—Chemical etching
- H10P50/644—Anisotropic liquid etching
Definitions
- the present invention relates to an epitaxial silicon wafer manufacturing method and an epitaxial silicon wafer.
- an epitaxial silicon wafer for a power MOS transistor is required to have a very low substrate resistivity.
- the molten silicon is used as an n-type dopant for adjusting the resistivity.
- a silicon wafer having a very low substrate resistivity doped with phosphorus (P) at a high concentration is being used (for example, see Patent Document 1).
- Patent Document 1 when an epitaxial film is grown on a silicon wafer to which phosphorus is added so that the resistivity is 0.9 m ⁇ ⁇ cm or less when a silicon single crystal is grown, a stacking fault (stacking fault, hereinafter, (SF) occurs in the epitaxial film, and this SF appears as a step on the surface of the silicon wafer, and the LPD (Light Point Defect) level on the surface of the silicon wafer is greatly deteriorated. ing.
- SF stacking fault
- an epitaxial film is grown after performing an argon annealing step in an argon gas atmosphere on a silicon wafer before the formation of the epitaxial film. Yes.
- An object of the present invention is to provide an epitaxial silicon wafer manufacturing method and an epitaxial silicon wafer capable of manufacturing a semiconductor device having sufficient electrical characteristics.
- dislocation defects DF were present (dislocation lines described later) as shown in FIG. 1A. Further, when the vertical cross section along the AA line in FIG. 1A is observed with a TEM, the dislocation defect DF extends obliquely with respect to the surface of the epitaxial film EP as shown in FIG. 1B.
- the dislocation defect DF has a size in plan view of about 1 ⁇ m to 2 ⁇ m, and has a (100) plane inclined as a main surface, and has a [011] direction, a [0-1-1] direction, a [0-11] direction. ] And dislocation lines having crystal orientation in either the [01-1] direction.
- dislocation defect DF cannot be detected before selective etching, it has crystal orientation in a state where selective etching is not performed, and an end portion on the surface side of the epitaxial film EP is located inside the epitaxial film EP. (The whole is located inside the epitaxial film), it is considered to exist as dislocation lines. Further, it can be inferred that dislocation lines are generated by minute pits in the silicon wafer caused by oxygen and phosphorus clusters, as in SF.
- the present inventor presumes that dislocation lines that do not appear on the surface of the epitaxial film EP deteriorate the electrical characteristics of the semiconductor device, and when the epitaxial film is formed on a silicon wafer having a predetermined plane orientation, The present invention has been completed by finding that the generation of dislocation lines having the property can be suppressed.
- the method for producing an epitaxial silicon wafer of the present invention is a method for producing an epitaxial silicon wafer in which an epitaxial film is provided on a silicon wafer having a resistivity of less than 1.0 m ⁇ ⁇ cm using phosphorus as a dopant.
- the silicon wafer whose main surface is an inclined surface) and whose [100] axis perpendicular to the (100) plane is inclined by 0 ° 5 ′ or more and 0 ° 25 ′ or less with respect to an axis perpendicular to the main surface.
- a pre-bake process of etching the silicon wafer after the pre-bake process Characterized in that at 1165 ° C. or less of the growth temperature of 1100 ° C. or more on the surface of and an epitaxial film growth step of growing the epitaxial layer.
- dislocation lines are less likely to be generated by reducing the crystal axis tilt angle of the silicon wafer and reducing the number of steps on the dislocation surface appearing on the (100) plane, that is, the (111) plane that is the slip plane.
- the silicon wafer is heat-treated in an argon gas atmosphere to form micro pits with oxygen and phosphorus clusters.
- micro pits are removed, and dislocation lines generated from the micro pits during epitaxial film growth are suppressed.
- the pre-bake step is etched with a machining allowance of 150 nm to 600 nm.
- minute pits caused by clusters that cannot be dissolved by heat treatment under an argon gas atmosphere can be removed by etching by a pre-baking process, and the generation of dislocation lines can be further suppressed.
- the epitaxial silicon wafer of the present invention is an epitaxial silicon wafer in which an epitaxial film is provided on a silicon wafer having a resistivity of less than 1.0 m ⁇ ⁇ cm using phosphorus as a dopant, and the silicon wafer has a (100) plane.
- the [100] axis perpendicular to the (100) plane is inclined by 0 ° 5 ′ or more and 0 ° 25 ′ or less with respect to the axis orthogonal to the main surface, with the inclined surface as the main surface.
- the density of dislocation lines located entirely within the epitaxial film is 10 pieces / cm 2 or less.
- the present invention is preferably applied to a silicon wafer having a resistivity of less than 0.9 m ⁇ ⁇ cm using phosphorus as a dopant. Furthermore, it is more preferable to apply to a silicon wafer having a resistivity of less than 0.8 m ⁇ ⁇ cm.
- a plan view of a dislocation line. 1B is a photograph of a longitudinal sectional view taken along the line AA in FIG. 1A.
- 1 is a cross-sectional view of an epitaxial silicon wafer according to an embodiment of the present invention. Explanatory drawing of the inclination direction of the [100] axis
- Explanatory drawing which shows the relationship between the residence time and resistivity in 570 degreeC +/- 70 degreeC in each solidification rate of the silicon single crystal of the comparative example 2 and Example 2 in the said Example, and the acquisition position of a silicon wafer.
- Explanatory drawing which shows the relationship of the residence time and resistivity in 570 degreeC +/- 70 degreeC in each solidification rate of the silicon single crystal of the comparative example 3 and Example 3 in the said Example, and the acquisition position of a silicon wafer.
- the graph which shows the relationship between the distance from the center of the epitaxial silicon wafer in the said Example, and the defect density inside an epitaxial film.
- the epitaxial silicon wafer EW includes a silicon wafer WF and an epitaxial film EP provided on the silicon wafer WF.
- the silicon wafer WF has a diameter of 199.8 mm or more and 200.2 mm or less, and contains phosphorus so that the electric resistivity is less than 1.0 m ⁇ ⁇ cm.
- the silicon wafer WF has a surface with an inclined (100) plane as a main surface WF1, and as shown in FIG.
- the [100] axis perpendicular to the (100) plane is perpendicular to the main surface WF1 [ 001] direction, [00-1] direction, [010] direction, [0-10] direction, or any one direction between them, 0 ° 5 ′ or more and 0 ° 25 ′ or less Just tilted.
- the density of dislocation lines having crystal orientation and the entirety located inside the epitaxial film EP is 10 pieces / cm 2 or less, and the generation of dislocation lines is suppressed. .
- the density of SF observed on the surface of the epitaxial silicon wafer EW is 1 piece / cm 2 or less.
- the method for manufacturing the epitaxial silicon wafer EW includes a wafer preparation step S1, an argon annealing step S2, a pre-baking step S3, and an epitaxial film growth step S4.
- a silicon wafer WF having the above-described configuration is prepared.
- phosphorus is contained so that the resistivity is 0.5 m ⁇ ⁇ cm or more and less than 1.0 m ⁇ ⁇ cm, and the central axis coincides with the [001] axis perpendicular to the (100) plane.
- a silicon single crystal to be manufactured may be manufactured, and the silicon single crystal may be sliced not by a plane orthogonal to the central axis but by an inclined plane with respect to the orthogonal plane.
- a silicon single crystal whose central axis is inclined by 0 ° 5 ′ or more and 0 ° 25 ′ or less with respect to the [100] axis perpendicular to the (100) plane is manufactured, and the silicon single crystal is orthogonal to the central axis. You may slice with. In addition, the following can be illustrated as manufacturing conditions of the said silicon single crystal.
- Phosphorus concentration 7.38 ⁇ 10 19 atoms / cm 3 or more 1.64 ⁇ 10 20 atoms / cm 3 or less
- Oxygen concentration 2 ⁇ 10 17 atoms / cm 3 or more 20 ⁇ 10 17 atoms / cm 3 (ASTM F121-1979 )
- lapping, chemical etching, mirror polishing, and other processes are performed on the obtained silicon wafer WF as necessary.
- a heat treatment is performed on the silicon wafer WF at a temperature of 1200 ° C. or higher and 1220 ° C. or lower in an argon gas atmosphere.
- the heat treatment time is preferably from 30 minutes to 90 minutes. If it is less than 30 minutes, there is a problem that SF is frequently generated when an epitaxial silicon wafer EW is manufactured using this silicon wafer WF, and if it exceeds 90 minutes, there is a problem that slip dislocation occurs. It is preferable to use a batch furnace that can anneal a plurality of silicon wafers WF at a time.
- the clusters generated in the silicon wafer WF are dissolved or eliminated or the number of micro pits can be reduced.
- the surface of the silicon wafer WF is etched.
- the silicon wafer WF is heat-treated under the following conditions in the epitaxial apparatus used in the epitaxial film growth step S4.
- Atmosphere Hydrogen gas, Hydrogen chloride gas Flow rate of hydrogen gas: 40 SLM Hydrogen chloride gas flow rate: 1 SLM Heat treatment temperature: 1190 ° C (1050 ° C to 1250 ° C) Heat treatment time: 30 seconds (30 seconds to 300 seconds)
- the temperature is raised in an atmosphere containing only hydrogen gas, and when the temperature reaches 1050 ° C. or higher and 1250 ° C.
- the machining allowance of the silicon wafer WF in the pre-baking step S3 is preferably 150 nm or more and 600 nm or less, and more preferably 500 nm ⁇ 100 nm.
- the outermost layer is etched in addition to the clusters existing in the outermost layer of the silicon wafer WF.
- the number of minute pits existing after the pre-baking step S3 can be reduced as compared with the case where the process is performed in a gas atmosphere containing only hydrogen.
- the epitaxial film EP is grown on the etched surface of the silicon wafer WF after the pre-baking step S3, for example, under the following conditions.
- Dopant gas phosphine (PH 3 ) gas
- Raw material source gas trichlorosilane (SiHCl 3 ) gas
- Carrier gas hydrogen gas Growth temperature: 1100 ° C. to 1165 ° C.
- Epitaxial film thickness 2 ⁇ m (1 ⁇ m to 10 ⁇ m)
- Resistivity epi film resistivity
- the number of steps of the dislocation surface appearing on the (100) plane, that is, the (111) plane, which is a slip surface, is reduced, and 1100 for a silicon wafer in which dislocation lines are difficult to occur
- the epitaxial film is grown at a low temperature of less than °C, the Terrace is wide and the energy of the silicon is small, so the supplied silicon cannot reach the Kink position, and abnormal growth occurs with the silicon remaining on the Terrace as the nucleus. Hillock defects are likely to occur. Therefore, by performing high temperature growth of the epitaxial film at 1100 ° C.
- the solidification rate means the ratio of the pulling weight of the silicon single crystal to the initial charge weight of the melt initially stored in the crucible.
- This silicon single crystal is sliced not by a plane orthogonal to the central axis but by a plane inclined with respect to this plane, and the plane with the (100) plane inclined as the main surface, as shown in Table 1, is perpendicular to the (100) plane.
- a silicon wafer was obtained in which the [100] axis was inclined by 0 ° 43 ′ in the [010] direction with respect to the axis perpendicular to the main surface.
- the silicon wafer of Comparative Example 1 was obtained from the intermediate position BM of the bottom region, where the upper end side in the pulling direction is the top region, the lower end side is the bottom region, and the middle region is between the top region and the bottom region.
- the residence time at 570 ° C. ⁇ 70 ° C. in the intermediate position BM was 40 minutes or less.
- the substrate resistivity of the silicon wafer of Comparative Example 1 was 0.8 m ⁇ ⁇ cm or more and less than 0.9 m ⁇ ⁇ cm.
- an argon annealing process was performed on the silicon wafer.
- heat treatment was performed at a temperature of 1200 ° C. for 30 minutes in an argon gas atmosphere.
- the prebaking process was performed with respect to the silicon wafer.
- heat treatment was performed for 30 seconds at a temperature of 1190 ° C. in a gas atmosphere containing hydrogen and hydrogen chloride. The stock removal at this time was 160 nm.
- Comparative Example 2 As shown in FIG. 5, a silicon single crystal was manufactured under the same conditions as in Comparative Example 1 except that the amount of phosphorus added was adjusted so that the resistivity at each solidification rate was lower than that in Comparative Example 1. Then, a silicon wafer having the same plane orientation as that of Comparative Example 1 was obtained from an intermediate position BM in the same bottom region as that of Comparative Example 1 in this silicon single crystal. The substrate resistivity of the silicon wafer of Comparative Example 2 was less than 0.7 m ⁇ ⁇ cm. Thereafter, an argon annealing step, a pre-bake step, and an epitaxial film growth step were performed under the same conditions as in Comparative Example 1, and a sample of Comparative Example 2 was obtained.
- Comparative Example 3 As shown in FIG. 6, a silicon wafer having the same plane orientation as that of Comparative Example 1 was obtained from the middle position MM of the middle region in the silicon single crystal manufactured in Comparative Example 2. The residence time at 570 ° C. ⁇ 70 ° C. in the intermediate position MM was 390 minutes or more. The substrate resistivity of the silicon wafer of Comparative Example 3 was 0.7 m ⁇ ⁇ cm or more and less than 0.8 m ⁇ ⁇ cm. Thereafter, an argon annealing step, a prebake step, and an epitaxial film growth step were performed under the same conditions as in Comparative Example 1, and a sample of Comparative Example 3 was obtained.
- a silicon single crystal was manufactured under the same conditions as in Comparative Example 2 as shown in FIG.
- the silicon single crystal is sliced from the same intermediate position MM as that of Comparative Example 3 in a plane that is not orthogonal to the central axis, and a plane with an inclined (100) plane is defined as a main surface and [100] plane perpendicular to the (100) plane [100]
- the silicon wafers of Comparative Examples 4 and 6 were obtained in which the axis was inclined by 0 ° 30 ′ in the [010] direction with respect to the axis orthogonal to the main surface.
- the surface with the (100) plane inclined is the main surface, and the [100] axis perpendicular to the (100) plane is 0 ° 45 in the [010] direction with respect to the axis perpendicular to the main surface.
- the silicon wafers of Comparative Examples 5 and 7 inclined by ′ were obtained.
- the substrate resistivity of the silicon wafers of Comparative Examples 4 to 7 was 0.7 m ⁇ ⁇ cm or more and less than 0.8 m ⁇ ⁇ cm.
- an argon annealing process, a pre-bake process, and an epitaxial film growth process were performed on the silicon wafers of Comparative Examples 4 and 5 under the same conditions as in Comparative Example 1 except that the growth temperature in the epitaxial film growth process was set to 1100 ° C. Samples of Comparative Examples 4 and 5 were obtained. Further, the silicon wafers of Comparative Examples 6 and 7 were the same as Comparative Example 4 except that the heat treatment was performed at a temperature of 1220 ° C. for 60 minutes in the argon annealing process and the processing time in the prebaking process was 90 seconds. Under conditions, an argon annealing step, a pre-bake step, and an epitaxial film growth step were performed, and samples of Comparative Examples 6 and 7 were obtained.
- Example 1 A silicon single crystal was manufactured under the same conditions as in Comparative Example 1 as shown in FIG.
- the silicon single crystal is sliced from an intermediate position BM of the bottom region with a plane that is not orthogonal to the central axis, and a plane with an inclined (100) plane is defined as the main surface, and as shown in Table 1, the (100) plane A silicon wafer was obtained in which the [100] axis perpendicular to the axis was inclined by 0 ° 15 ′ in the [010] direction with respect to the axis perpendicular to the main surface.
- the substrate resistivity of the silicon wafer of Example 1 was 0.8 m ⁇ ⁇ cm or more and less than 0.9 m ⁇ ⁇ cm.
- an argon annealing process was performed on the silicon wafer under the same conditions as in Comparative Example 1 except that the temperature was 1220 ° C. and the time was 60 minutes.
- the prebaking process was performed on the silicon wafer under the same conditions as in Comparative Example 1 except that the temperature was 1190 ° C., the time was 90 seconds, and the machining allowance was 500 nm.
- the epitaxial film growth process was performed on the same conditions as the comparative example 1 except having set temperature to 1100 degreeC with respect to the etching surface of a silicon wafer, and the sample of Example 1 was obtained.
- Examples 2 and 3 A silicon single crystal is manufactured under the same conditions as in Comparative Example 2 as shown in FIG. 5, and the plane orientation is the same as in Example 1 from the same intermediate positions BM and MM as Comparative Examples 2 and 3 in this silicon single crystal. , 3 silicon wafers were obtained.
- the substrate resistivity of the silicon wafer of Example 2 was less than 0.7 m ⁇ ⁇ cm
- the substrate resistivity of the silicon wafer of Example 3 was 0.7 m ⁇ ⁇ cm or more and less than 0.8 m ⁇ ⁇ cm.
- an argon annealing step, a pre-bake step, and an epitaxial film growth step were performed under the same conditions as in Example 1 to obtain samples of Examples 2 and 3.
- Examples 4 to 8 A silicon single crystal was manufactured under the same conditions as in Comparative Example 2 as shown in FIG.
- the silicon single crystal is sliced from the same intermediate position MM as that of Comparative Example 3 in a plane that is not orthogonal to the central axis, and a plane with an inclined (100) plane is defined as a main surface and [100] plane perpendicular to the (100) plane [100]
- the silicon wafers of Examples 4 and 7 in which the axis was inclined by 0 ° 5 ′ in the [010] direction with respect to the axis orthogonal to the main surface were obtained.
- the surface with the (100) plane inclined is defined as the main surface, and the [100] axis perpendicular to the (100) plane is 0 ° 15 in the [010] direction with respect to the axis orthogonal to the main surface.
- a silicon wafer of Example 5 inclined by ' was obtained.
- the surface with the (100) plane inclined is defined as the main surface, and the [100] axis perpendicular to the (100) plane is 0 ° 25 in the [010] direction with respect to the axis perpendicular to the main surface.
- the silicon wafers of Examples 6 and 8 inclined by ' were obtained.
- the substrate resistivity of the silicon wafers of Examples 4 to 8 was 0.7 m ⁇ ⁇ cm or more and less than 0.8 m ⁇ ⁇ cm.
- the silicon wafers of Examples 4 to 6 were subjected to an argon annealing process, a pre-bake process, and an epitaxial film growth process under the same conditions as in Comparative Example 4 to obtain samples of Examples 4 to 6. Moreover, the argon annealing process, the prebaking process, and the epitaxial film growth process were performed on the silicon wafers of Examples 7 and 8 under the same conditions as in Comparative Example 6 to obtain samples of Examples 7 and 8.
- the tilt angle of the [100] axis of the silicon wafer is 0 ° 5 ′ or more and 0 ° 25 ′ or less, the density of LPD may be lowered even if the growth temperature in the epitaxial film growth step is 1100 ° C. or more. It could be confirmed.
- Comparative Examples 2 and 3 a defect was detected.
- 1600 defects / cm 2 or more were detected in the entire observation region.
- Comparative Example 2 although it was 148 pieces / cm 2 at the center of the epitaxial silicon wafer, it gradually increased toward the outer edge, and was almost at the same level as Comparative Example 3 at the outer edge. Then, when the defects detected in Comparative Examples 2 and 3 were observed with a TEM, the surface with the (100) plane inclined as shown in FIGS.
- Comparative Example 2 has a low substrate resistivity despite using a silicon wafer obtained from the same part at a stay time of 570 ° C. ⁇ 70 ° C. in the silicon single crystal. Dislocation lines were generated, and no dislocation lines were generated in Comparative Example 1 having a high substrate resistivity. From this, it was confirmed that the substrate resistivity of the silicon wafer affects the generation of dislocation lines inside the epitaxial film.
- the comparative example 3 has a longer residence time of 570 ° C. ⁇ 70 ° C., although the silicon wafer obtained from the same silicon single crystal is used. There were many occurrences. From this, it was confirmed that the residence time of 570 ° C. ⁇ 70 ° C. in the silicon single crystal affects the generation of dislocation lines inside the epitaxial film.
- the comparative example 3 had a higher substrate resistivity than the comparative example 2, more dislocation lines were generated than the comparative example 2. From this, it was confirmed that the residence time of 570 ° C. ⁇ 70 ° C. in the silicon single crystal has a greater influence on the generation of dislocation lines inside the epitaxial film than the substrate resistivity.
- the inclination direction of the [100] axis with respect to the axis orthogonal to the main surface is opposite to that in the first to eighth embodiments ([0-10] direction) or orthogonal ([001], [00-1]), Alternatively, it can be presumed that the same results as in Examples 1 to 8 can be obtained even when tilted in any one direction between them. This is because the number of steps of the (111) plane, which is a dislocation surface appearing in the (100) plane, does not depend on the direction of crystal axis tilt. Furthermore, it can be assumed that the same results as in Examples 1 to 8 can be obtained regardless of the tilt angle of the [100] axis from 0 ° 5 ′ to 0 ° 25 ′.
- the temperature at the time of epitaxial film growth determines whether or not nucleation starts on Terrace. Therefore, if it is in the range of 0 ° 5 ′ or more and 0 ° 25 ′ or less, the growth temperature is appropriately set to 1100 ° C. or more. By selecting, it is presumed that hillock defects due to abnormal growth centering on silicon remaining on Terrace can be suppressed.
- EP Epitaxial film
- EW Epitaxial silicon wafer
- WF Silicon wafer
- WF1 Main surface.
Landscapes
- Chemical & Material Sciences (AREA)
- Metallurgy (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Mechanical Engineering (AREA)
- Inorganic Chemistry (AREA)
- Electrochemistry (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Chemical Vapour Deposition (AREA)
- Recrystallisation Techniques (AREA)
Abstract
Description
このような不具合を解消するために、特許文献1には、エピタキシャル膜形成前のシリコンウェーハに対して、アルゴンガス雰囲気下でアルゴンアニール工程を行った後、エピタキシャル膜を成長させることが開示されている。
特許文献1の方法で製造されたエピタキシャルシリコンウェーハであって、表面検査装置によってSFを検出できなかったエピタキシャルシリコンウェーハのエピタキシャル膜を、M-Dash液((フッ酸(50wt%):硝酸(70wt%):酢酸(100wt%):H2O=1:3:8~12:0.17)+硝酸銀水溶液(0.005~0.05g/L))(SEMI MF1809-0704参照)で選択エッチングした。選択エッチング後のエピタキシャル膜表面をTEM(Transmission Electron Microscope:透過型電子顕微鏡)で観察すると、図1Aに示すように、転位欠陥DFが存在していた(後述する、転位線)。さらに、図1AのA-A線に沿う縦断面をTEMで観察すると、図1Bに示すように、転位欠陥DFは、エピタキシャル膜EP表面に対して斜めに延びていた。
この転位欠陥DFは、平面視のサイズが1μm~2μm程度であって、(100)面が傾斜した面を主表面とし、[011]方向、[0-1-1]方向、[0-11]方向および[01-1]方向のいずれかの方向に結晶方位性を有した転位線であった。
また、転位線は、SFと同様に、酸素とリンのクラスターに起因するシリコンウェーハの微小ピットによって発生していると推測できる。
以上の結果から、本発明者は、エピタキシャル膜EP表面に現れない転位線が半導体デバイスの電気特性を悪化させていると推測し、所定の面方位のシリコンウェーハにエピタキシャル膜を形成すると、面方位性を有する転位線の発生を抑制できることを見出し、本発明を完成させた。
その結果、転位線の密度が10個/cm2以下であり、転位線の発生が抑制されたエピタキシャルシリコンウェーハを得ることができる。したがって、このようなエピタキシャルシリコンウェーハ用いて、十分な電気特性を有する半導体デバイスを製造できる。
本発明をリンをドーパントとした抵抗率が0.9mΩ・cm未満のシリコンウェーハに適用することが好ましい。さらに、抵抗率が0.8mΩ・cm未満のシリコンウェーハに適用することがさらに好ましい。
以下、本発明の一実施形態について図面を参照して説明する。
〔エピタキシャルシリコンウェーハの構成〕
図2Aに示すように、エピタキシャルシリコンウェーハEWは、シリコンウェーハWFと、このシリコンウェーハWFに設けられたエピタキシャル膜EPとを備えている。
シリコンウェーハWFは、直径が199.8mm以上200.2mm以下であり、電気抵抗率が1.0mΩ・cm未満になるようにリンを含んでいる。シリコンウェーハWFは、(100)面が傾斜した面を主表面WF1とし、図2Bに示すように、(100)面に垂直な[100]軸が主表面WF1に直交する軸に対して、[001]方向、[00-1]方向、[010]方向、[0-10]方向のうちいずれか一方向、あるいは、これらの間の任意の一方向に0°5′以上0°25′以下だけ傾斜している。
このような構成のエピタキシャルシリコンウェーハEWにおいて、結晶方位性を有し、全体がエピタキシャル膜EP内部に位置する転位線の密度は、10個/cm2以下であり転位線の発生が抑制されている。また、エピタキシャルシリコンウェーハEWの表面で観察されるSFの密度は、1個/cm2以下である。
次に、上記エピタキシャルシリコンウェーハEWの製造方法について説明する。
エピタキシャルシリコンウェーハEWの製造方法は、図3に示すように、ウェーハ準備工程S1と、アルゴンアニール工程S2と、プリベーク工程S3と、エピタキシャル膜成長工程S4とを備えている。
なお、上記シリコン単結晶の製造条件としては、以下のものが例示できる。
リン濃度:7.38×1019atoms/cm3以上1.64×1020atoms/cm3以下
酸素濃度:2×1017atoms/cm3以上20×1017atoms/cm3(ASTM F121-1979)以下
そして、この得られたシリコンウェーハWFに対し、必要に応じて、ラッピング、化学エッチング、鏡面研磨、その他の処理を行う。
また、1回で複数のシリコンウェーハWFをアニール可能なバッチ炉を用いることが好ましい。
雰囲気:水素ガス、塩化水素ガス
水素ガスの流量:40SLM
塩化水素ガスの流量:1SLM
熱処理温度:1190℃(1050℃以上1250℃以下)
熱処理時間:30秒(30秒以上300秒以下)
なお、プリベーク工程S3において水素および塩化水素を含むガス雰囲気を形成するに際し、まず水素ガスのみの雰囲気下で昇温し、1050℃以上1250℃以下の温度に到達したら、塩化水素ガスを供給することが好ましい。このようなタイミングで塩化水素ガスを供給することによって、エピタキシャルシリコンウェーハEWに曇りが発生してしまうことと、スリップ転位の発生を抑制することができる。
また、プリベーク工程S3によるシリコンウェーハWFの取代は、150nm以上600nm以下が好ましく、500nm±100nmであることがさらに好ましい。
ドーパントガス:フォスフィン(PH3)ガス
原料ソースガス:トリクロロシラン(SiHCl3)ガス
キャリアガス:水素ガス
成長温度:1100℃以上1165℃以下
エピタキシャル膜の厚さ:2μm(1μm以上10μm以下)
抵抗率(エピ膜抵抗率):0.2Ω・cm(0.01Ω・cm以上10Ω・cm以下)
シリコンウェーハの結晶軸傾け角度を大きくすると、エピタキシャル膜成長工程において転位線が発生しやすく、成長温度が高い場合、その転位は、線状のみならず面のずれも伴ってSFとしてエピタキシャル膜表面で検出される。しかし、成長温度が低い場合、転位線は、エピタキシャル膜表面まで突き抜けずに、エピタキシャル膜内部に終端が位置してしまうと考えられる。
また、結晶軸傾け角度を小さくすることで、(100)面に現れる転位面、すなわちすべり面である(111)面のStep数が低減され、転位線が発生し難いシリコンウェーハに対して、1100℃未満のエピタキシャル膜低温成長を実施した場合は、Terraceが広くかつシリコンが持つエネルギーが小さいため、供給されたシリコンがKink位置に到達できず、Terrace上に留まったシリコンを核として異常成長が行われ、ヒロック欠陥が発生しやすい。
そこで、結晶軸傾け角度が小さく転位線が発生し難いシリコンウェーハに対して、1100℃以上のエピタキシャル膜高温成長を実施することで、エピタキシャル膜表面にヒロック欠陥が存在せず、エピタキシャル膜内部にも転位線が発生しないエピタキシャルウェーハを得ることができる。その結果、結晶方位性を有し、全体がエピタキシャル膜EP内部に位置する転位線の密度が10個/cm2以下であり転位線の発生が抑制されたエピタキシャルシリコンウェーハEWを得ることができる。なお、エピタキシャル膜成長温度は、1165℃を超えるとエピタキシャル膜にスリップ転位が発生するので好ましくない。
〔比較例1〕
まず、チョクラルスキー法によって、直胴部の抵抗率が1.0mΩ・cm未満となるようにリンを添加し、中心軸が[100]軸と一致しかつ直径が200mmのシリコン単結晶を製造した。このときの各固化率における570℃±70℃での滞在時間は、図4に示すように、固化率が約56%までの領域は、約280分から約530分までほぼ直線的に長くなり、これに続く約68%までの領域は、約530分から約40分までほぼ直線的に短くなり、これに続く領域は、約40分から約30分までほぼ直線的に短くなった。また、このときの各固化率における抵抗率は、図4に示すように、下端に向かうほど低くなった。
なお、固化率とは、最初に坩堝に貯留された融液の初期チャージ重量に対するシリコン単結晶の引上げ重量の割合をいう。
比較例1のシリコンウェーハは、引き上げ方向上端側をトップ領域、下端側をボトム領域、トップ領域とボトム領域との間をミドル領域とした場合、ボトム領域の中間位置BMから取得した。中間位置BMにおける570℃±70℃での滞在時間は、40分以下であった。比較例1のシリコンウェーハの基板抵抗率は0.8mΩ・cm以上0.9mΩ・cm未満であった。
この後、シリコンウェーハに対して、プリベーク工程を行った。この工程は、水素および塩化水素を含むガス雰囲気下において、1190℃の温度で30秒の熱処理を行った。このときの取代は、160nmであった。
ドーパントガス:フォスフィン(PH3)ガス
原料ソースガス:トリクロロシラン(SiHCl3)ガス
キャリアガス:水素ガス
成長温度:1040℃
エピタキシャル膜の厚さ:2μm
エピタキシャル膜の抵抗率:0.2Ω・cm
図5に示すように、各固化率における抵抗率が比較例1と比べて低くなるように、リンの添加量を調整したこと以外は、比較例1と同じ条件でシリコン単結晶を製造した。そして、このシリコン単結晶における比較例1と同じボトム領域の中間位置BMから、面方位が比較例1と同じシリコンウェーハを取得した。比較例2のシリコンウェーハの基板抵抗率は、0.7mΩ・cm未満であった。
その後、比較例1と同じ条件で、アルゴンアニール工程、プリベーク工程、エピタキシャル膜成長工程を行い、比較例2のサンプルを得た。
図6に示すように、比較例2で製造したシリコン単結晶におけるミドル領域の中間位置MMから、面方位が比較例1と同じシリコンウェーハを取得した。中間位置MMにおける570℃±70℃での滞在時間は、390分以上であった。比較例3のシリコンウェーハの基板抵抗率は0.7mΩ・cm以上0.8mΩ・cm未満であった。
その後、比較例1と同じ条件で、アルゴンアニール工程、プリベーク工程、エピタキシャル膜成長工程を行い、比較例3のサンプルを得た。
図5に示すような比較例2と同じ条件でシリコン単結晶を製造した。このシリコン単結晶における比較例3と同じ中間位置MMから、その中心軸に対する直交面ではない面でスライスし、(100)面が傾斜した面を主表面とし、(100)面に垂直な[100]軸が主表面に直交する軸に対して[010]方向に0°30′だけ傾斜した比較例4,6のシリコンウェーハを取得した。また、上記中間位置MMから、(100)面が傾斜した面を主表面とし、(100)面に垂直な[100]軸が主表面に直交する軸に対して[010]方向に0°45′だけ傾斜した比較例5,7のシリコンウェーハを取得した。比較例4~7のシリコンウェーハの基板抵抗率は0.7mΩ・cm以上0.8mΩ・cm未満であった。
図4に示すような比較例1と同じ条件でシリコン単結晶を製造した。このシリコン単結晶におけるボトム領域の中間位置BMから、その中心軸に対する直交面ではない面でスライスし、(100)面が傾斜した面を主表面とし、表1に示すように、(100)面に垂直な[100]軸が主表面に直交する軸に対して[010]方向に0°15′だけ傾斜したシリコンウェーハを取得した。実施例1のシリコンウェーハの基板抵抗率は0.8mΩ・cm以上0.9mΩ・cm未満であった。
この後、シリコンウェーハに対して、温度を1190℃、時間を90秒、取代を500nmとしたこと以外は、比較例1と同じ条件でプリベーク工程を行った。
そして、シリコンウェーハのエッチング面に対して、温度を1100℃にしたこと以外は、比較例1と同じ条件でエピタキシャル膜成長工程を行い、実施例1のサンプルを得た。
図5に示すような比較例2と同じ条件でシリコン単結晶を製造し、このシリコン単結晶における比較例2,3と同じ中間位置BM,MMから、面方位が実施例1と同じ実施例2,3のシリコンウェーハを取得した。実施例2のシリコンウェーハの基板抵抗率は、0.7mΩ・cm未満であり、実施例3のシリコンウェーハの基板抵抗率は、0.7mΩ・cm以上0.8mΩ・cm未満であった。
その後、実施例1と同じ条件で、アルゴンアニール工程、プリベーク工程、エピタキシャル膜成長工程を行い、実施例2,3のサンプルを得た。
図5に示すような比較例2と同じ条件でシリコン単結晶を製造した。このシリコン単結晶における比較例3と同じ中間位置MMから、その中心軸に対する直交面ではない面でスライスし、(100)面が傾斜した面を主表面とし、(100)面に垂直な[100]軸が主表面に直交する軸に対して[010]方向に0°5′だけ傾斜した実施例4,7のシリコンウェーハを取得した。また、上記中間位置MMから、(100)面が傾斜した面を主表面とし、(100)面に垂直な[100]軸が主表面に直交する軸に対して[010]方向に0°15′だけ傾斜した実施例5のシリコンウェーハを取得した。さらに、上記中間位置MMから、(100)面が傾斜した面を主表面とし、(100)面に垂直な[100]軸が主表面に直交する軸に対して[010]方向に0°25′だけ傾斜した実施例6,8のシリコンウェーハを取得した。実施例4~8のシリコンウェーハの基板抵抗率は0.7mΩ・cm以上0.8mΩ・cm未満であった。
〔エピタキシャル膜表面の評価〕
表面検査装置(KLA-Tencor社製SP-1、DCNモード)を用いて、比較例1~3、実施例1~3のエピタキシャル膜表面で観察される90nmサイズ以上のLPDをカウントし、単位面積あたりの個数(密度)を評価した。その結果を表1に示す。
このことから、シリコンウェーハの[100]軸の傾け角度が0°25′を超える場合、エピタキシャル膜成長工程における成長温度が1100℃以上になるとLPDの密度が高くなり、1100℃未満になるとLPDの密度が低くなることが確認できた。
また、シリコンウェーハの[100]軸の傾け角度が0°5′以上0°25′以下の場合、エピタキシャル膜成長工程における成長温度が1100℃以上であっても、LPDの密度が低くなることが確認できた。
比較例1~7、実施例1~8の厚さが2μmのエピタキシャル膜に対し、上述のM-Dash液を用いて1μmの選択エッチングを行った。そして、エッチング面を光学顕微鏡(NIKON、OPTIPHOT88)で観察し、エピタキシャルシリコンウェーハの中心から外縁に向かう直線状の複数箇所において、1.4μmサイズ以上の欠陥をカウントした。その単位面積あたりの個数(密度)を図7に示す。
そして、比較例2,3で検出された欠陥をTEMで観察したところ、図1A,図1Bに示すような(100)面が傾斜した面を主表面とし、[011]方向、[0-1-1]方向、[0-11]方向および[01-1]方向のいずれかの方向に結晶方位性を有する転位欠陥DFであった。このことから、比較例2,3のエピタキシャル膜には、結晶方位性を有し、全体がエピタキシャル膜内部に位置する転位線が存在していることがわかった。
このことから、シリコンウェーハの基板抵抗率は、エピタキシャル膜内部における転位線の発生に影響を及ぼすことが確認できた。
このことから、シリコン単結晶における570℃±70℃の滞在時間は、エピタキシャル膜内部における転位線の発生に影響を及ぼすことが確認できた。
このことから、シリコン単結晶における570℃±70℃の滞在時間は、基板抵抗率よりもエピタキシャル膜内部における転位線の発生に及ぼす影響が大きいことが確認できた。
このことから、エピタキシャル膜成長工程の成長温度は、エピタキシャル膜内部における転位線の発生に及ぼす影響が大きいことが確認できた。
このことから、[100]軸の傾け角度を所定の値に設定することで、すなわちシリコンウェーハの面方位を所定の方位に設定することで、転位線の発生抑制できることがわかった。
さらに、[100]軸の傾け角度が0°5′以上0°25′以下のいずれの角度であっても、実施例1~8と同様の結果が得られると推測できる。その理由は、エピタキシャル膜成長時の温度によってTerrace上で核形成が始まるか否かが決まるので、0°5′以上0°25′以下の範囲であれば、成長温度を1100℃以上で適切に選択することにより、Terrace上に留まったシリコンを核とした異常成長によるヒロック欠陥を抑制できると推定される。
Claims (3)
- リンをドーパントとした抵抗率が1.0mΩ・cm未満のシリコンウェーハに、エピタキシャル膜が設けられたエピタキシャルシリコンウェーハの製造方法であって、
(100)面が傾斜した面を主表面とし、前記(100)面に垂直な[100]軸が前記主表面に直交する軸に対して0°5′以上0°25′以下だけ傾斜した前記シリコンウェーハを準備するウェーハ準備工程と、
前記シリコンウェーハに対し、アルゴンガス雰囲気下において1200℃以上1220℃以下の温度で30分以上の熱処理を行うアルゴンアニール工程と、
前記アルゴンアニール工程後のシリコンウェーハの表面をエッチングするプリベーク工程と、
前記プリベーク工程後のシリコンウェーハの表面に1100℃以上1165℃以下の成長温度で前記エピタキシャル膜を成長させるエピタキシャル膜成長工程とを備えていることを特徴とするエピタキシャルシリコンウェーハの製造方法。 - 請求項1に記載のエピタキシャルシリコンウェーハの製造方法において、
前記プリベーク工程は、150nm以上600nm以下の取代でエッチングすることを特徴とするエピタキシャルシリコンウェーハの製造方法。 - リンをドーパントとした抵抗率が1.0mΩ・cm未満のシリコンウェーハに、エピタキシャル膜が設けられたエピタキシャルシリコンウェーハであって、
前記シリコンウェーハは、(100)面が傾斜した面を主表面とし、前記(100)面に垂直な[100]軸が前記主表面に直交する軸に対して0°5′以上0°25′以下だけ傾斜しており、
結晶方位性を有し、全体が前記エピタキシャル膜の内部に位置する転位線の密度が10個/cm2以下であることを特徴とするエピタキシャルシリコンウェーハ。
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2019511179A JP6973475B2 (ja) | 2017-04-06 | 2018-03-28 | エピタキシャルシリコンウェーハの製造方法およびエピタキシャルシリコンウェーハ |
| CN201880021911.9A CN110603350B (zh) | 2017-04-06 | 2018-03-28 | 外延硅晶片的制造方法及外延硅晶片 |
| US16/497,869 US10867791B2 (en) | 2017-04-06 | 2018-03-28 | Method for manufacturing epitaxial silicon wafer and epitaxial silicon wafer |
| KR1020197030558A KR102279113B1 (ko) | 2017-04-06 | 2018-03-28 | 에피택셜 실리콘 웨이퍼의 제조 방법 및 에피택셜 실리콘 웨이퍼 |
| DE112018001919.5T DE112018001919B4 (de) | 2017-04-06 | 2018-03-28 | Verfahren zum herstellen eines siliziumepitaxialwafers und siliziumepitaxialwafer |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2017-076034 | 2017-04-06 | ||
| JP2017076034 | 2017-04-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2018186248A1 true WO2018186248A1 (ja) | 2018-10-11 |
Family
ID=63712954
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2018/012640 Ceased WO2018186248A1 (ja) | 2017-04-06 | 2018-03-28 | エピタキシャルシリコンウェーハの製造方法およびエピタキシャルシリコンウェーハ |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US10867791B2 (ja) |
| JP (1) | JP6973475B2 (ja) |
| KR (1) | KR102279113B1 (ja) |
| CN (1) | CN110603350B (ja) |
| DE (1) | DE112018001919B4 (ja) |
| WO (1) | WO2018186248A1 (ja) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109791878B (zh) * | 2016-08-10 | 2023-05-09 | 胜高股份有限公司 | 外延硅晶片及外延硅晶片的制造方法 |
| JP7491705B2 (ja) * | 2020-02-19 | 2024-05-28 | グローバルウェーハズ・ジャパン株式会社 | 半導体シリコンウェーハの製造方法 |
| JP7770907B2 (ja) * | 2021-12-22 | 2025-11-17 | グローバルウェーハズ・ジャパン株式会社 | シリコンエピタキシャル基板の製造方法およびシリコンエピタキシャル基板 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004091234A (ja) * | 2002-08-30 | 2004-03-25 | Sumitomo Mitsubishi Silicon Corp | エピタキシャルウェーハとその製造方法 |
| WO2016174997A1 (ja) * | 2015-04-30 | 2016-11-03 | 株式会社Sumco | エピタキシャルシリコンウェーハの製造方法 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3081706B2 (ja) * | 1992-06-12 | 2000-08-28 | 株式会社東芝 | 半導体装置用基板 |
| JP3601383B2 (ja) * | 1999-11-25 | 2004-12-15 | 信越半導体株式会社 | エピタキシャル成長用シリコンウエーハ及びエピタキシャルウエーハ並びにその製造方法 |
| JP2004009123A (ja) * | 2002-06-10 | 2004-01-15 | Toshiba Corp | 絞り加工部品、絞り加工部品の製造方法およびその装置 |
| JP4190906B2 (ja) * | 2003-02-07 | 2008-12-03 | 信越半導体株式会社 | シリコン半導体基板及びその製造方法 |
| JP4682508B2 (ja) * | 2003-11-14 | 2011-05-11 | 信越半導体株式会社 | シリコンエピタキシャルウェーハの製造方法 |
| JP5544986B2 (ja) * | 2010-04-01 | 2014-07-09 | 信越半導体株式会社 | 貼り合わせsoiウェーハの製造方法、及び貼り合わせsoiウェーハ |
| JP5845143B2 (ja) | 2012-06-29 | 2016-01-20 | 株式会社Sumco | エピタキシャルシリコンウェーハの製造方法、および、エピタキシャルシリコンウェーハ |
| FR2995913B1 (fr) * | 2012-09-24 | 2014-10-10 | Commissariat Energie Atomique | Procede de formation d'une couche de silicium epitaxiee. |
| US10233562B2 (en) * | 2013-04-24 | 2019-03-19 | Sumco Techxiv Corporation | Method for producing single crystal, and method for producing silicon wafer |
| JP6052189B2 (ja) * | 2014-01-16 | 2016-12-27 | 信越半導体株式会社 | シリコン単結晶ウェーハの熱処理方法 |
-
2018
- 2018-03-28 JP JP2019511179A patent/JP6973475B2/ja active Active
- 2018-03-28 WO PCT/JP2018/012640 patent/WO2018186248A1/ja not_active Ceased
- 2018-03-28 CN CN201880021911.9A patent/CN110603350B/zh active Active
- 2018-03-28 US US16/497,869 patent/US10867791B2/en active Active
- 2018-03-28 KR KR1020197030558A patent/KR102279113B1/ko active Active
- 2018-03-28 DE DE112018001919.5T patent/DE112018001919B4/de active Active
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004091234A (ja) * | 2002-08-30 | 2004-03-25 | Sumitomo Mitsubishi Silicon Corp | エピタキシャルウェーハとその製造方法 |
| WO2016174997A1 (ja) * | 2015-04-30 | 2016-11-03 | 株式会社Sumco | エピタキシャルシリコンウェーハの製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| DE112018001919B4 (de) | 2022-09-22 |
| US20200027727A1 (en) | 2020-01-23 |
| CN110603350A (zh) | 2019-12-20 |
| KR102279113B1 (ko) | 2021-07-16 |
| CN110603350B (zh) | 2021-07-16 |
| JPWO2018186248A1 (ja) | 2020-01-16 |
| DE112018001919T5 (de) | 2020-01-09 |
| JP6973475B2 (ja) | 2021-12-01 |
| US10867791B2 (en) | 2020-12-15 |
| KR20190124793A (ko) | 2019-11-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR100573473B1 (ko) | 실리콘 웨이퍼 및 그 제조방법 | |
| TWI552202B (zh) | Epitaxial silicon wafers and their manufacturing methods | |
| KR100741540B1 (ko) | 에피텍셜 성장용 실리콘 웨이퍼와 에피텍셜 웨이퍼, 및 그제조방법 | |
| CN115135816A (zh) | 半导体硅晶片的制造方法 | |
| US20200020817A1 (en) | Epitaxial silicon wafer | |
| JP6973475B2 (ja) | エピタキシャルシリコンウェーハの製造方法およびエピタキシャルシリコンウェーハ | |
| TW201719758A (zh) | 磊晶矽晶圓 | |
| JP2025157587A (ja) | シリコンウェーハおよびエピタキシャルシリコンウェーハ | |
| TWI741950B (zh) | 矽晶圓的製造方法 | |
| JP2025146998A (ja) | シリコンウェーハおよびエピタキシャルシリコンウェーハ | |
| JP4465141B2 (ja) | シリコンエピタキシャルウェーハ及びその製造方法 | |
| JP2010287885A (ja) | シリコンウェーハおよびその製造方法 | |
| JP7757917B2 (ja) | シリコンウェーハおよびエピタキシャルシリコンウェーハ | |
| CN116072515B (zh) | 硅晶片和外延硅晶片 | |
| CN115135818A (zh) | 半导体硅晶片的制造方法 | |
| US12527054B2 (en) | Silicon wafer and epitaxial silicon wafer | |
| US20250185323A1 (en) | Silicon wafer and epitaxial silicon wafer | |
| JP7775800B2 (ja) | シリコンウェーハおよびエピタキシャルシリコンウェーハ | |
| US20230243062A1 (en) | Silicon wafer and method for producing silicon wafer |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 18780478 Country of ref document: EP Kind code of ref document: A1 |
|
| ENP | Entry into the national phase |
Ref document number: 2019511179 Country of ref document: JP Kind code of ref document: A |
|
| ENP | Entry into the national phase |
Ref document number: 20197030558 Country of ref document: KR Kind code of ref document: A |
|
| 122 | Ep: pct application non-entry in european phase |
Ref document number: 18780478 Country of ref document: EP Kind code of ref document: A1 |
