WO2015076128A1 - 炭化珪素半導体装置および炭化珪素半導体装置の製造方法 - Google Patents
炭化珪素半導体装置および炭化珪素半導体装置の製造方法 Download PDFInfo
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- WO2015076128A1 WO2015076128A1 PCT/JP2014/079630 JP2014079630W WO2015076128A1 WO 2015076128 A1 WO2015076128 A1 WO 2015076128A1 JP 2014079630 W JP2014079630 W JP 2014079630W WO 2015076128 A1 WO2015076128 A1 WO 2015076128A1
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- silicon carbide
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- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 title claims description 113
- 229910010271 silicon carbide Inorganic materials 0.000 title claims description 111
- 239000004065 semiconductor Substances 0.000 title claims description 96
- 238000004519 manufacturing process Methods 0.000 title claims description 23
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims abstract description 260
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 126
- 229910021334 nickel silicide Inorganic materials 0.000 claims abstract description 63
- RUFLMLWJRZAWLJ-UHFFFAOYSA-N nickel silicide Chemical compound [Ni]=[Si]=[Ni] RUFLMLWJRZAWLJ-UHFFFAOYSA-N 0.000 claims abstract description 63
- 239000010936 titanium Substances 0.000 claims abstract description 31
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 30
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 29
- 238000010438 heat treatment Methods 0.000 claims abstract description 17
- MTPVUVINMAGMJL-UHFFFAOYSA-N trimethyl(1,1,2,2,2-pentafluoroethyl)silane Chemical compound C[Si](C)(C)C(F)(F)C(F)(F)F MTPVUVINMAGMJL-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229910052751 metal Inorganic materials 0.000 claims description 41
- 239000002184 metal Substances 0.000 claims description 41
- 239000000758 substrate Substances 0.000 claims description 34
- 238000000034 method Methods 0.000 claims description 29
- 238000000151 deposition Methods 0.000 claims description 27
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- 238000010030 laminating Methods 0.000 claims description 3
- 230000015572 biosynthetic process Effects 0.000 abstract description 10
- 239000010931 gold Substances 0.000 abstract description 10
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 abstract description 8
- 229910052737 gold Inorganic materials 0.000 abstract description 8
- 238000005245 sintering Methods 0.000 abstract description 3
- 239000010410 layer Substances 0.000 description 219
- 235000012431 wafers Nutrition 0.000 description 40
- 230000035882 stress Effects 0.000 description 32
- 239000012535 impurity Substances 0.000 description 9
- 238000000926 separation method Methods 0.000 description 8
- 238000004544 sputter deposition Methods 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 7
- 229910052799 carbon Inorganic materials 0.000 description 6
- 238000010586 diagram Methods 0.000 description 6
- 238000002441 X-ray diffraction Methods 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- 238000000137 annealing Methods 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
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- 238000005468 ion implantation Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 230000008646 thermal stress Effects 0.000 description 2
- 241001050985 Disco Species 0.000 description 1
- 229910005881 NiSi 2 Inorganic materials 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
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- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
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- 150000002815 nickel Chemical class 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
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Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L29/00—Semiconductor devices specially adapted for rectifying, amplifying, oscillating or switching and having potential barriers; Capacitors or resistors having potential barriers, e.g. a PN-junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof ; Multistep manufacturing processes therefor
- H01L29/40—Electrodes ; Multistep manufacturing processes therefor
- H01L29/43—Electrodes ; Multistep manufacturing processes therefor characterised by the materials of which they are formed
- H01L29/45—Ohmic electrodes
-
- 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
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/06—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
- C23C14/14—Metallic material, boron or silicon
- C23C14/18—Metallic material, boron or silicon on other inorganic substrates
- C23C14/185—Metallic material, boron or silicon on other inorganic substrates by cathodic sputtering
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/0445—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising crystalline silicon carbide
- H01L21/048—Making electrodes
- H01L21/0485—Ohmic electrodes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L29/00—Semiconductor devices specially adapted for rectifying, amplifying, oscillating or switching and having potential barriers; Capacitors or resistors having potential barriers, e.g. a PN-junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof ; Multistep manufacturing processes therefor
- H01L29/02—Semiconductor bodies ; Multistep manufacturing processes therefor
- H01L29/12—Semiconductor bodies ; Multistep manufacturing processes therefor characterised by the materials of which they are formed
- H01L29/16—Semiconductor bodies ; Multistep manufacturing processes therefor characterised by the materials of which they are formed including, apart from doping materials or other impurities, only elements of Group IV of the Periodic Table
- H01L29/1608—Silicon carbide
Definitions
- the present invention relates to a silicon carbide semiconductor device and a method for manufacturing a silicon carbide semiconductor device.
- semiconductor devices that have been used as power devices are mainly those that use silicon (Si) as a semiconductor material.
- silicon carbide (SiC) which is a semiconductor having a wider band gap than silicon (hereinafter referred to as a wide gap semiconductor)
- SiC silicon carbide
- the speed has a physical property value of twice. For this reason, in order to produce (manufacture) a power device capable of operating at high temperature with high dielectric breakdown voltage and low loss, research on applying silicon carbide has been actively conducted in recent years.
- the structure of such a power device is mainly a vertical semiconductor device having a back electrode having a low-resistance ohmic electrode on the back side.
- Various materials and structures are used for the back electrode of the vertical semiconductor device, and one of them is a laminate of a titanium (Ti) layer, a nickel (Ni) layer, and a silver (Ag) layer.
- Ti titanium
- Ni nickel
- Au silver
- back electrodes made of a laminate of a titanium layer, a nickel layer, and a gold layer for example, refer to Patent Document 2 below
- a nickel layer is formed on a semiconductor substrate made of silicon carbide (hereinafter referred to as a SiC substrate), and then heat treatment is performed.
- a method has been proposed in which the contact (electrical contact portion) between the SiC substrate and the nickel silicide layer is made ohmic contact by siliciding the layer to form a nickel silicide layer (see, for example, Patent Documents 1 and 2 below) .)
- Patent Documents 1 and 2 when the back electrode is formed on the nickel silicide layer, there is a problem that the back electrode is easily peeled off from the nickel silicide layer.
- a titanium layer, a nickel layer, and a silver layer are sequentially stacked on the nickel silicide layer.
- a method for suppressing peeling of the back electrode by forming the back electrode is proposed (for example, see Patent Document 3 below).
- a method of improving the adhesion of the back electrode by forming the back electrode on the nickel silicide layer after removing the metal carbide formed on the surface of the nickel silicide layer is proposed. (For example, see Patent Document 4 below).
- the back electrode is formed using the techniques of Patent Documents 3 and 4, the adhesion between the nickel silicide layer and the lowermost titanium layer of the back electrode is low, and the semiconductor wafer is diced into individual chips.
- the back electrode is peeled off from the nickel silicide layer.
- a nickel layer is formed on a SiC substrate, and subsequently a heat treatment is performed to form a nickel silicide layer, thereby forming an ohmic contact between the SiC substrate and the nickel silicide layer.
- the nickel silicide layer is generated by a solid phase reaction between nickel and silicon carbide represented by the following formula (1).
- the carbon (C) produced by the reaction of the above formula (1) is dispersed throughout the inside of the nickel silicide layer as a supersaturated state in which the crystalline state is not stable or as a fine precipitate.
- the carbon dispersed inside the nickel silicide layer is discharged at a stroke by heat treatment performed after the nickel silicide layer is formed, and is deposited (aggregated) as a precipitate such as graphite on the surface or inside of the nickel silicide layer.
- the precipitate formed by the agglomeration of carbon is brittle and has poor adhesion. Therefore, there is a problem that the precipitate is easily broken even by a slight stress and the back electrode formed on the nickel silicide layer is peeled off.
- An object of the present invention is to provide a silicon carbide semiconductor device and a method for manufacturing the silicon carbide semiconductor device capable of suppressing the peeling of the back electrode in order to solve the above-described problems caused by the prior art.
- a silicon carbide semiconductor device has the following characteristics.
- a metal layer that forms an ohmic contact with the semiconductor substrate is provided on a semiconductor substrate made of silicon carbide.
- a metal electrode laminate in which at least a titanium layer and a nickel layer are sequentially laminated. And the residual stress of the said nickel layer is 200 Mpa or less.
- the silicon carbide semiconductor device according to the present invention is characterized in that, in the above-described invention, the residual stress of the nickel layer is 100 MPa or less.
- the nickel layer has a thickness of the nickel layer of x [nm] and a deposition rate of the nickel layer of y [nm / second]. In this case, it is characterized in that it is formed under a condition satisfying 0.0 ⁇ y ⁇ 0.0013x + 2.0.
- the silicon carbide semiconductor device according to the present invention is characterized in that, in the above-described invention, the nickel layer is formed under a condition satisfying 0.0 ⁇ y ⁇ 0.0015x + 1.2.
- the metal layer is a nickel silicide layer containing titanium carbide.
- a method for manufacturing a silicon carbide semiconductor device has the following characteristics. First, a first step of forming a metal layer on a semiconductor substrate made of silicon carbide is performed. Next, a second step of forming an ohmic contact between the semiconductor substrate and the metal layer is performed by heat treatment. Next, a third step is performed in which at least a titanium layer and a nickel layer are sequentially laminated on the metal layer to form a metal electrode laminate. In the third step, when the thickness of the nickel layer is x [nm] and the deposition rate of the nickel layer is y [nm / sec], 0.0 ⁇ y ⁇ 0.0013x + 2 The nickel layer is formed under a condition satisfying.
- the nickel layer is formed under a condition satisfying 0.0 ⁇ y ⁇ 0.0015x + 1.2.
- the method for manufacturing a silicon carbide semiconductor device according to the present invention is characterized in that, in the above-described invention, in the third step, the nickel layer is formed by a vapor deposition method.
- the metal layer containing titanium and nickel is formed on the semiconductor substrate, and in the second step, heat treatment is performed.
- the semiconductor substrate and the metal layer are reacted to form a nickel silicide layer containing titanium carbide to form an ohmic contact between the semiconductor substrate and the nickel silicide layer.
- the silicon carbide substrate and the metal layer by determining the thickness of the nickel layer and the deposition rate of the nickel layer so that the residual stress of the nickel layer constituting the metal electrode laminate is 200 MPa or less, the silicon carbide substrate and the metal layer , And the adhesion between the metal layer and the back electrode laminate can be improved. Thereby, it can suppress that the electrode (metal layer and metal electrode laminated body) on a silicon carbide substrate peels.
- the silicon carbide semiconductor device and the method for manufacturing the silicon carbide semiconductor device according to the present invention it is possible to suppress the peeling of the back electrode.
- FIG. 1 is a cross-sectional view showing a state during the manufacture of the silicon carbide semiconductor device according to the embodiment.
- FIG. 2 is a cross-sectional view showing a state during the manufacture of the silicon carbide semiconductor device according to the embodiment.
- FIG. 3 is a cross-sectional view showing a state during the manufacture of the silicon carbide semiconductor device according to the embodiment.
- FIG. 4 is a cross-sectional view showing a state during the manufacture of the silicon carbide semiconductor device according to the embodiment.
- FIG. 5 is a cross-sectional view showing a state during the manufacture of the silicon carbide semiconductor device according to the embodiment.
- FIG. 6 is a chart showing the relationship between the film forming conditions of the nickel layer constituting the back electrode laminate of the silicon carbide semiconductor device according to the embodiment and the adhesion of the back electrode.
- FIG. 7 is a characteristic diagram showing the relationship between the film forming conditions of the nickel layer constituting the back electrode laminate of the silicon carbide semiconductor device according to the embodiment and the residual stress of the nickel layer.
- FIG. 8 is a characteristic diagram showing the relationship between the thickness of the nickel layer constituting the back electrode laminate of the silicon carbide semiconductor device according to the embodiment and the deposition rate of the nickel layer.
- a silicon carbide semiconductor device includes a back electrode in which a contact (electrical contact portion) with a semiconductor substrate (hereinafter referred to as a SiC substrate) made of silicon carbide (SiC) is an ohmic contact.
- the back electrode is formed by sequentially laminating a nickel silicide layer (metal layer forming an ohmic contact with the SiC substrate) and a back electrode laminate (metal electrode laminate) on the SiC substrate.
- a titanium (Ti) layer, a nickel (Ni) layer, and a gold (Au) layer are sequentially laminated from the nickel silicide layer side.
- a semiconductor region corresponding to the element structure is provided inside the SiC substrate.
- the element structure of the silicon carbide semiconductor device front surface electrode, semiconductor region inside the SiC substrate, and the like
- a semiconductor wafer made of silicon carbide (hereinafter referred to as a SiC wafer) using a metal film forming apparatus such as a sputtering apparatus or a vacuum evaporation apparatus.
- a metal film forming apparatus such as a sputtering apparatus or a vacuum evaporation apparatus.
- a metal layer containing titanium and nickel is formed on the back surface of the substrate.
- the SiC wafer is heated by high-temperature heat treatment to sinter (sinter) the metal layer containing titanium and nickel, thereby forming a nickel silicide layer containing titanium carbide (TiC).
- sinter sinter
- TiC nickel silicide layer containing titanium carbide
- a back electrode laminate is formed by sequentially laminating a titanium layer, a nickel layer, and a gold layer on the nickel silicide layer.
- the nickel silicide layer containing titanium carbide generated (formed) as described above exhibits good adhesion with the titanium layer, which is the lowermost layer of the back electrode laminate, and has a function of suppressing peeling of the back electrode laminate.
- the SiC substrate, the nickel silicide layer, and the nickel silicide layer are reduced by reducing the internal stress (residual stress) remaining in the back electrode stack after the back electrode stack is formed. It has been found that the adhesion between the back electrode laminate and the back electrode laminate can be improved, and peeling of the back electrode (nickel silicide layer and back electrode laminate) can be further suppressed.
- the thickness and deposition rate of the nickel layer laminated on the titanium layer, which is the lowermost layer of the back electrode laminate, are optimized, and the residual stress of this nickel layer is set to 200 MPa or less.
- the film forming conditions for forming the nickel layer constituting the back electrode laminate are as follows: the nickel layer thickness is x [nm], and the nickel layer forming speed is Is y [nm / sec], the following equation (2) is preferably satisfied, and desirably the following equation (3) is satisfied.
- 1 to 5 are cross-sectional views showing a state during the manufacture of the silicon carbide semiconductor device according to the embodiment. Description and illustration of the formation process of the front surface element structure (front surface electrode and semiconductor region on the front surface side of the substrate) is omitted, but the front surface element structure is the back surface element structure (back surface electrode). In parallel with the formation of the semiconductor region on the back surface side of the substrate), it may be formed at a predetermined timing by a general method.
- n-type impurities such as phosphorus (P) are ion-implanted 11 into the back surface of the n-type SiC wafer 1. To do.
- the SiC wafer 1 is heated using, for example, a rapid annealing (RTA) apparatus equipped with an infrared lamp, and the n-type impurities implanted into the back surface of the SiC wafer 1 are activated.
- the heat treatment for activating the impurities may be performed for about 180 seconds at a temperature of about 1620 ° C. in an argon (Ar) atmosphere, for example.
- an n-type semiconductor region (not shown) having an impurity concentration higher than that of SiC wafer 1 is formed in the front surface layer of SiC wafer 1.
- the contact resistance between the SiC wafer 1 and a nickel silicide layer described later can be reduced.
- a protective resist film (not shown) for surface protection having a thickness of 2 ⁇ m, for example, is formed on the front surface of the SiC wafer 1 using, for example, a spin coater.
- the natural oxide film formed on the back surface of the SiC wafer 1 is removed using, for example, a hydrofluoric acid buffer.
- the protective resist film on the front surface of the SiC wafer 1 is removed using, for example, a resist removing solution.
- the titanium layer 2 and the nickel layer 3 are sequentially formed on the back surface (that is, on the n-type semiconductor region) of the SiC wafer 1 using a metal film forming apparatus such as a sputtering apparatus (for example). Form.
- the thickness of the titanium layer 2 and the nickel layer 3 may be, for example, about 60 nm and about 40 nm, respectively.
- the state of the nickel silicide layer 4 is determined by the annealing treatment after the film formation, so the method for forming the metal layers (titanium layer 2 and nickel layer 3) that are precursors thereof is not limited. .
- the adhesion strength of the deposited film (metal layer) is higher in the sputtering method than in the vapor deposition method, the sputtering method is important when it is important to prevent film peeling (peeling of the metal layer) after deposition. It is preferable to form a metal layer to be the nickel silicide layer 4 using
- the substrate (wafer) temperature becomes high during the formation of the metal layer. For this reason, there is a risk of film peeling due to thermal stress after completion of the metal layer deposition (when returning to room temperature). This phenomenon of film peeling occurs when the thickness of the nickel silicide layer 4 is increased. When the nickel silicide layer 4 having a thickness of 100 nm or less as in the present invention is formed, there is no problem. In the case of the back electrode layer (back electrode laminate 8 described later), the nickel layer 6 constituting the back electrode layer is thick (about 400 nm in the following examples). The thermal stress change is large, and peeling may occur. For this reason, when forming a back surface electrode layer, it is preferable to use a vapor deposition method.
- the SiC wafer 1 is heated using, for example, a high-speed annealing apparatus equipped with an infrared lamp, and the titanium layer 2 and the nickel layer 3 are sintered (sintered).
- the heat treatment for sintering may be performed for about 120 seconds at a temperature of about 950 ° C. in an argon atmosphere, for example.
- silicon (Si) atoms in SiC wafer 1 react with nickel atoms in nickel layer 3 to form nickel silicide layer 4, and ohmic contact between SiC wafer 1 and nickel silicide layer 4 is formed.
- carbon (C) atoms in the SiC wafer 1 react with titanium atoms in the titanium layer 2 to generate titanium carbide in the nickel silicide layer 4.
- a protective resist film (not shown) for surface protection having a thickness of 2 ⁇ m, for example, is formed on the front surface of the SiC wafer 1 using, for example, a spin coater.
- the carbon atoms in the nickel silicide layer 4 are deposited on the surface of the nickel silicide layer 4 (surface opposite to the SiC wafer 1 side) during the heat treatment for sintering.
- the thin carbon deposition layer (not shown) having a small thickness is removed by, for example, reverse sputtering 12 for removing impurities by colliding with ionized argon.
- the reverse sputtering 12 for removing the carbon deposition layer may be performed at a high frequency (RF) power of about 300 W for about 180 seconds under a pressure of about 6 Pa.
- the titanium layer 5, the nickel layer 6, and the gold (Au) layer 7 are sequentially deposited (formed) on the nickel silicide layer 4 using a metal film forming apparatus such as a vapor deposition apparatus.
- a metal film forming apparatus such as a vapor deposition apparatus.
- the back electrode laminate 8 is formed.
- the nickel layer 6 constituting the back electrode laminated body 8 is formed under film forming conditions that satisfy the above formula (2) (desirably, the above formula (3)).
- the thicknesses of the titanium layer 5, the nickel layer 6 and the gold layer 7 constituting the back electrode laminate 8 may be, for example, 70 nm, 400 nm and 200 nm, respectively.
- SiC wafer 1 is diced (cut) into individual chips to complete the silicon carbide semiconductor device according to the embodiment.
- Example 1 a plurality of SiC wafers 1 (samples) on which a back electrode structure (nickel silicide layer 4, back electrode stack 8 and semiconductor region on the back side of the substrate) is formed.
- Example 1 Each sample of Example 1 includes nickel layers 6 having different thicknesses formed at different film formation speeds in the range of 0.3 nm / second to 1.2 nm / second.
- the thickness of the titanium layer 5 is equal to 70 nm for each sample, and the thickness of the gold layer 7 is equal to 200 nm for each sample.
- the front surface element structure is not formed.
- Example 1 For each sample of Example 1, first, the residual stress of the nickel layer 6 constituting the back electrode laminate 8 was evaluated. Specifically, a sample (semiconductor wafer) is attached to a sample holder, an X-ray diffraction pattern is measured using a wide-angle X-ray diffraction (micro-part X-ray diffraction) method, and the residual stress at the center of the wafer is measured. evaluated. The sin 2 ⁇ method (side tilt method) was used for stress evaluation, and the diffraction line peak on the (331) plane of nickel was used as an index for evaluating residual stress.
- a sample semiconductor wafer
- an X-ray diffraction pattern is measured using a wide-angle X-ray diffraction (micro-part X-ray diffraction) method
- the sin 2 ⁇ method side tilt method
- the diffraction line peak on the (331) plane of nickel was used as an index for evaluating residual stress.
- Orientation evaluation was performed using an X-ray diffraction apparatus (model name: D8 DISCOVER ⁇ HR Hybrid (registered trademark)) manufactured by Bruker AXS Co., Ltd.
- CuK ⁇ rays parallel beam optical system using a multilayer mirror
- the voltage and current of the X-ray tube were 50 kV and 22 mA, respectively.
- a pinhole slit having a diameter of 1 mm was used as a divergence slit for determining the width of incident X-rays.
- a two-dimensional PSPC Position Sensitive Proportional Counter
- X-ray diffraction patterns were measured when the angle ⁇ between the normal of the sample surface and the normal of the crystal lattice plane was 0 °, 20 °, 30 °, 40 °, 50 °, 60 °, and 70 °.
- the integration time per frame was 600 seconds / frame.
- interval (d value) of the sample was measured with the X-ray-diffraction apparatus, and the residual stress (sigma) [MPa] concerning a sample was computed from the change of a lattice plane space
- each chip was 5 mm ⁇ 5 mm in size.
- DISCO Corporation's dicing machine model name: DAD3350 (registered trademark)
- dicing blade model name: NBC-Z, outer diameter x thickness x inner diameter: 56 mm x 0.05 mm x 40 mm
- the rotation speed of the spindle (rotary shaft) was 40000 rpm, the feed rate was 1 mm / second, and the cutting depth (depth at which the dicing blade penetrates the sample and cuts the dicing tape) was 0.045 mm.
- FIG. 6 is a chart showing the relationship between the film forming conditions of the nickel layer constituting the back electrode laminate of the silicon carbide semiconductor device according to the embodiment and the adhesion of the back electrode.
- FIG. 6 shows the presence or absence of back electrode peeling for each nickel layer 6 deposition rate (Ni deposition rate) and for each nickel layer 6 thickness (Ni layer thickness).
- FIG. 7 shows the relationship between the residual stress ⁇ of the nickel layer 6 calculated using the above equation (4), the thickness of the nickel layer 6 and the film formation rate.
- FIG. 7 is a characteristic diagram showing the relationship between the film forming conditions of the nickel layer constituting the back electrode laminate of the silicon carbide semiconductor device according to the embodiment and the residual stress of the nickel layer.
- an approximate curve of the residual stress ⁇ of the nickel layer 6 when the thickness of the nickel layer 6 (the thickness of the Ni layer) is changed is illustrated for each deposition rate of the nickel layer 6.
- FIG. 7 also shows the adhesion test results of the back electrode of FIG. 6 ( ⁇ : no peeling, ⁇ : peeling mixed (corresponding to micro peeling in FIG. 6), x: peeling).
- the residual stress ⁇ of the nickel layer 6 decreases as the thickness of the nickel layer 6 decreases and the deposition rate of the nickel layer 6 decreases.
- the residual stress ⁇ of the nickel layer 6 is 200 MPa or less, regardless of the thickness of the nickel layer 6 and the deposition rate, “ ⁇ : no peeling” or “ ⁇ : peeling mixed” occurs, and the back electrode peels off. It was confirmed that they were suppressed (the range of residual stress in which ⁇ marks are distributed (hereinafter referred to as a peeled mixed region) and the range of residual stresses in which ⁇ marks are distributed (hereinafter referred to as a non-peeled region).
- peeling generation region range of residual stress in which x marks are distributed
- the allowable range of the residual stress ⁇ of the nickel layer 6 is 200 MPa or less, and the nickel layer 6 is thinned so that the residual stress ⁇ of the nickel layer 6 is 200 MPa or less, preferably 100 MPa or less. It was confirmed that by slowing down the film formation rate, it was possible to make it difficult for the back electrode to peel off.
- FIG. 8 is a characteristic diagram showing the relationship between the thickness of the nickel layer constituting the back electrode laminate of the silicon carbide semiconductor device according to the embodiment and the deposition rate of the nickel layer.
- the abscissa indicates the nickel layer 6 thickness (Ni layer thickness)
- the ordinate indicates the nickel layer 6 deposition rate (Ni deposition rate).
- the relationship between a region and a separation occurrence region is shown. As shown in FIG.
- the separation occurrence region and the separation mixed region are It was confirmed that the boundary line is the following equation (5), and the boundary line between the separation mixed region and the separation non-occurrence region is the following equation (6). Therefore, the thickness of the nickel layer 6 and the deposition rate of the nickel layer 6 are determined so as to be closer to the origin (0, 0) than the following equation (5) (that is, within the range satisfying the above equation (2)). Thus, it was confirmed that peeling of the back electrode can be suppressed.
- the thickness of the nickel layer 6 and the deposition rate of the nickel layer 6 are determined so as to be closer to the origin (0, 0) than the following formula (6) (that is, within the range satisfying the formula (3)). Thus, it was confirmed that the back electrode was not peeled off.
- the thickness of the nickel layer 6 is 400 nm, it is possible to prevent the back surface electrode from peeling off by setting the deposition rate of the nickel layer 6 to 0.5 nm / second or less.
- the embodiment by determining the thickness of the nickel layer and the deposition rate of the nickel layer so that the residual stress of the nickel layer constituting the back electrode laminate is 200 MPa or less.
- the adhesion between the SiC wafer and the nickel silicide layer, and between the nickel silicide layer and the back electrode stack can be improved.
- achieved ohmic contact with a SiC wafer Can be produced.
- the present invention is not limited to the above-described embodiment, and various modifications can be made without departing from the spirit of the present invention.
- the case where the ohmic contact between the SiC wafer and the back surface electrode is formed is described as an example, but the present invention can be applied to the case where the ohmic contact between the SiC wafer and the front surface electrode is formed.
- the present invention is applicable to a silicon carbide semiconductor device provided with a metal electrode that forms an ohmic contact with a SiC wafer.
- a metal electrode that forms an ohmic contact with a SiC wafer.
- MOSFET Metal Oxide Semiconductor Field Transistor
- a type bipolar transistor IGBT: Insulated Gate Bipolar Transistor
- a Schottky diode In the above-described embodiment, an epitaxial wafer in which a SiC epitaxial layer is stacked on a SiC wafer may be used instead of the SiC wafer.
- the case where the n-type semiconductor region is formed in the surface layer on the back surface of the n-type SiC wafer has been described as an example.
- p-type impurities are ion-implanted into the back surface of the n-type SiC wafer to form p.
- a type impurity may be formed.
- the conductivity type (n-type, p-type) of the semiconductor layer or the semiconductor substrate is inverted.
- the silicon carbide semiconductor device and the method for manufacturing the silicon carbide semiconductor device according to the present invention are useful for a power semiconductor device including a metal electrode that forms an ohmic contact with a silicon carbide semiconductor.
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Abstract
Description
実施の形態にかかる炭化珪素半導体装置の構造について説明する。実施の形態にかかる炭化珪素半導体装置は、炭化珪素(SiC)からなる半導体基板(以下、SiC基板とする)とのコンタクト(電気的接触部)がオーミックコンタクトとなる裏面電極を備える。裏面電極は、SiC基板上にニッケルシリサイド層(SiC基板とのオーミックコンタクトを形成する金属層)および裏面電極積層体(金属電極積層体)が順に積層されてなる。裏面電極積層体は、ニッケルシリサイド層側から例えばチタン(Ti)層、ニッケル(Ni)層および金(Au)層が順に積層されてなる。SiC基板の内部には、素子構造に応じた半導体領域が設けられている。炭化珪素半導体装置の素子構造(おもて面電極やSiC基板の内部の半導体領域など)は、設計条件に応じて種々変更可能であるため、説明を省略する。
2 ニッケルシリサイド層となるチタン層
3 ニッケルシリサイド層となるニッケル層
4 ニッケルシリサイド層
5 裏面電極積層体を構成するチタン層
6 裏面電極積層体を構成するニッケル層
7 裏面電極積層体を構成する金層
8 裏面電極積層体
11 イオン注入
12 逆スパッタ
Claims (9)
- 炭化珪素からなる半導体基板上に設けられ、前記半導体基板とのオーミックコンタクトを形成する金属層と、
前記金属層上に、少なくともチタン層およびニッケル層を順に積層してなる金属電極積層体と、
を備え、
前記ニッケル層の残留応力は、200MPa以下であることを特徴とする炭化珪素半導体装置。 - 前記ニッケル層の残留応力は、100MPa以下であることを特徴とする請求項1に記載の炭化珪素半導体装置。
- 前記ニッケル層は、前記ニッケル層の厚さをx[nm]とし、前記ニッケル層の成膜速度をy[nm/秒]としたときに、0.0<y<-0.0013x+2.0を満たす条件で形成されていることを特徴とする請求項1に記載の炭化珪素半導体装置。
- 前記ニッケル層は、0.0<y<-0.0015x+1.2を満たす条件で形成されていることを特徴とする請求項3に記載の炭化珪素半導体装置。
- 前記金属層は、チタンカーバイドを含むニッケルシリサイド層であることを特徴とする請求項1~4のいずれか一つに記載の炭化珪素半導体装置。
- 炭化珪素からなる半導体基板上に金属層を形成する第1工程と、
熱処理により、前記半導体基板と前記金属層とのオーミックコンタクトを形成する第2工程と、
前記金属層上に、少なくともチタン層およびニッケル層を順に積層して金属電極積層体を形成する第3工程と、
を含み、
前記第3工程では、前記ニッケル層の厚さをx[nm]とし、前記ニッケル層の成膜速度をy[nm/秒]としたときに、0.0<y<-0.0013x+2.0を満たす条件で前記ニッケル層を形成することを特徴とする炭化珪素半導体装置の製造方法。 - 前記第3工程では、0.0<y<-0.0015x+1.2を満たす条件で前記ニッケル層を形成することを特徴とする請求項6に記載の炭化珪素半導体装置の製造方法。
- 前記第3工程では、蒸着法により前記ニッケル層を形成することを特徴とする請求項6に記載の炭化珪素半導体装置の製造方法。
- 前記第1工程では、前記半導体基板上にチタンおよびニッケルを含む前記金属層を形成し、
前記第2工程では、熱処理により前記半導体基板および前記金属層を反応させてチタンカーバイドを含むニッケルシリサイド層を形成して、前記半導体基板と前記ニッケルシリサイド層とのオーミックコンタクトを形成することを特徴とする請求項6~8のいずれか一つに記載の炭化珪素半導体装置の製造方法。
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CN201480028190.6A CN105308722B (zh) | 2013-11-22 | 2014-11-07 | 碳化硅半导体装置及碳化硅半导体装置的制造方法 |
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US10374050B2 (en) | 2019-08-06 |
US20160087061A1 (en) | 2016-03-24 |
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JP6390745B2 (ja) | 2018-09-19 |
EP2993690A4 (en) | 2017-01-18 |
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