US20100025695A1 - Annealing method for semiconductor device with silicon carbide substrate and semiconductor device - Google Patents
Annealing method for semiconductor device with silicon carbide substrate and semiconductor device Download PDFInfo
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- US20100025695A1 US20100025695A1 US11/813,621 US81362107A US2010025695A1 US 20100025695 A1 US20100025695 A1 US 20100025695A1 US 81362107 A US81362107 A US 81362107A US 2010025695 A1 US2010025695 A1 US 2010025695A1
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- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 title claims abstract description 92
- 239000000758 substrate Substances 0.000 title claims abstract description 71
- 238000000137 annealing Methods 0.000 title claims description 64
- 229910010271 silicon carbide Inorganic materials 0.000 title claims description 37
- 238000000034 method Methods 0.000 title claims description 26
- 239000004065 semiconductor Substances 0.000 title claims description 16
- 239000012535 impurity Substances 0.000 claims abstract description 44
- 239000010410 layer Substances 0.000 claims description 24
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- 239000002344 surface layer Substances 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 description 30
- 150000002500 ions Chemical class 0.000 description 21
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 20
- 230000004913 activation Effects 0.000 description 13
- 238000002513 implantation Methods 0.000 description 13
- 229910052782 aluminium Inorganic materials 0.000 description 12
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- 238000006243 chemical reaction Methods 0.000 description 5
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Images
Classifications
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- 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
- H01L21/0455—Making n or p doped regions or layers, e.g. using diffusion
- H01L21/046—Making n or p doped regions or layers, e.g. using diffusion using ion implantation
-
- 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
- H01L21/0455—Making n or p doped regions or layers, e.g. using diffusion
- H01L21/046—Making n or p doped regions or layers, e.g. using diffusion using ion implantation
- H01L21/0465—Making n or p doped regions or layers, e.g. using diffusion using ion implantation using masks
-
- 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
- H01L21/67—Apparatus specially adapted for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus specially adapted for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components ; Apparatus not specifically provided for elsewhere
- H01L21/67005—Apparatus not specifically provided for elsewhere
- H01L21/67011—Apparatus for manufacture or treatment
- H01L21/67098—Apparatus for thermal treatment
- H01L21/67109—Apparatus for thermal treatment mainly by convection
-
- 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
- H01L29/66—Types of semiconductor device ; Multistep manufacturing processes therefor
- H01L29/66007—Multistep manufacturing processes
- H01L29/66053—Multistep manufacturing processes of devices having a semiconductor body comprising crystalline silicon carbide
- H01L29/66068—Multistep manufacturing processes of devices having a semiconductor body comprising crystalline silicon carbide the devices being controllable only by the electric current supplied or the electric potential applied, to an electrode which does not carry the current to be rectified, amplified or switched, e.g. three-terminal devices
Definitions
- the present invention relates to an annealing method for activating an ion implanted region in a device including a silicon carbide (SiC) substrate having an ion implanted layer formed therein and a semiconductor device.
- SiC silicon carbide
- the present invention aims to solve the problems described above, and to provide an annealing method for annealing a device including a silicon carbide (SiC) substrate so that the surface flatness (RMS value) is controlled to be not greater than 6.0 nm, and further to provide a semiconductor device in which a high, electric activation can be accomplished while maintaining the surface flatness (RMS value) to be not greater than 2 nm, and preferably not greater than 1 nm by using this annealing method.
- SiC silicon carbide
- An annealing method for annealing a device including a silicon carbide (SiC) substrate includes a step of forming an impurity doped region in a silicon carbide (SiC) substrate and a step of annealing the impurity doped region in the silicon carbide (SiC) substrate, and it is specified that a partial pressure of H 2 O in an annealing atmosphere in the annealing step is not larger than 10 ⁇ 2 Pa.
- the silicon carbide (SiC) substrate has an epitaxial silicon carbide (SiC) crystalline layer as a surface layer, and an impurity doped region is formed in the silicon carbide (SiC) crystalline layer.
- an atmosphere for the annealing step has a partial pressure of H 2 O not larger than 10 ⁇ 3 Pa.
- the silicon carbide (SiC) substrate implanted with impurities is preferably annealed with being covered by a cap.
- the annealing step is carried out in a vacuum vessel capable of evacuating of air, and in one embodiment, the vacuum vessel is evacuated of air so that a pressure in the vacuum vessel is not greater than 10 ⁇ 4 Pa.
- a semiconductor device including a silicon carbide (SiC) substrate and an impurity doped region in the substrate, in which a surface flatness of the silicon carbide (SiC) substrate is not greater than 2 nm, and more preferably not greater than 1 nm in RMS value, and in one embodiment, the semiconductor device is a MOS field-effect transistor.
- An annealing method for activating a device including a silicon carbide (SiC) substrate sets a partial pressure of residual H 2 O in a vacuum vessel to be not larger than 10 ⁇ 2 Pa, and anneals, and whereby, an advantage is provided that a surface flatness of the silicon carbide (SiC) substrate can be controlled to be equal to or less than 2 nm (RMS value). Further, by setting the partial pressure of residual H 2 O in the vacuum vessel to be not larger than 10 ⁇ 3 Pa and annealing, an advantage is provided that a semiconductor device can be provided in which a high, electric activation can be easily accomplished while maintaining the surface flatness to be equal to or less than 1 nm (RMS value).
- FIG. 1A shows a silicon carbide (SiC) substrate having an epitaxial SiC layer
- FIG. 1B shows impurity implantation into the silicon carbide (SiC) substrate shown in FIG. 1A ;
- FIG. 1C shows annealing of the silicon carbide (SiC) substrate implanted with impurities in FIG. 1B ;
- FIG. 1D shows an annealing heating apparatus using a cap
- FIG. 1E shows annealing in which a cap layer is added
- FIG. 1F shows an annealing heating apparatus using SiH 4 addition and a vessel of silicon carbide
- FIG. 2 schematically shows an ion implantation system
- FIG. 3 is a cross-section view of a heating apparatus for annealing
- FIG. 4 shows surface irregularity on a silicon carbide (SiC) substrate generated from annealing
- FIG. 5 is a graph illustrating relationship between a partial pressure of residual H 2 O and the surface irregularity of a silicon carbide (SiC) substrate;
- FIG. 6 is a cross-section view of a heating apparatus using a cap having a through-hole for annealing
- FIG. 7A shows a first example of a cap having a through-hole
- FIG. 7B shows a second example of a cap having a through-hole
- FIG. 7C shows a third example of a cap having a through-hole
- FIG. 7D shows a fourth example of a cap having a through-hole
- FIG. 8A shows impurity implantation into a silicon carbide (SiC) substrate
- FIG. 8B shows annealing of the silicon carbide (SiC) substrate in FIG. 8A ;
- FIG. 9A and FIG. 9B show a process flow for manufacturing a silicon carbide (SiC)-DMOSFET.
- FIGS. 1A to 1F are process drawings illustrating steps of an annealing method for activating a device including a silicon carbide (SiC) substrate implanted with aluminum as atoms for impurity ions.
- SiC silicon carbide
- FIGS. 1A to 1F are process drawings illustrating steps of an annealing method for activating a device including a silicon carbide (SiC) substrate implanted with aluminum as atoms for impurity ions.
- SiC silicon carbide
- SiC silicon carbide
- SiC silicon carbide
- step flow growth Ext. Abst. 19th Conf. Solid State Devices and Materials (Tokyo, 1987) 227, N. Kuroda, K. Shibahara, W. S. Yoo, S. Nishino and H. Matsunami
- SiC epitaxial layer 2 A step of growing an SiC epitaxial layer 2 on a monocrystal silicon carbide (SiC) substrate 1 shown in FIG. 1A will be described.
- a surface of the monocrystal SiC substrate is etched at a temperature of about 1300° C. using HCl (flow rate: 1 mL/min.), and a damaged layer is removed.
- an epitaxial layer of silicon carbide (SiC) is grown (growth rate: 3 ⁇ m/hour) at a temperature of about 1500° C. using an SiH 4 gas (50 sccm, 1.0% H 2 dilution) and a C 3 H 8 gas (33 sccm, 1.0% H 2 dilution) as raw material gases, and an H 2 gas (flow rate: 3 sLm) as a carrier gas.
- an n-type epitaxial layer is formed.
- an epitaxial layer 2 of silicon carbide (SiC) (film thickness: 10 ⁇ m) is formed on the monocrystal silicon carbide (SiC) substrate 1 .
- the monocrystal silicon carbide (SiC) substrate and also the entire structure in which the epitaxial SiC layer is formed on the monocrystal substrate shown in FIG. 1A may be herein called the “silicon carbide (SiC) substrate” collectively.
- FIG. 2 shows an ion implantation system for selectively forming a well region or a contact region for manufacturing a device on a SiC substrate.
- Operation of the ion implantation system used in the present invention is as follows. Impurity material desired to implant is ionized using a filament or plasma in an ion source 21 in an ion gun 20 . Plasma (excited ion species) is extracted in a form of beam using an extraction electrode 22 . Only impurity ions desired to implant are extracted using an analyzing magnet 23 or an analyzer tube. Implantation energy is determined by an accelerating voltage between the ion source 21 and an end station 201 at an accelerating tube 24 . (The implantation energy determines an implantation depth).
- a beam 25 is scanned in order to uniformly implant the ions in a surface of a wafer 26 having a mask in which an ion inflow region is exposed.
- the wafer 26 may be rotated to improve uniformity, and it may be also heated to a high temperature to maintain crystallization.
- An implantation process for implanting impurities into a SiC substrate used in the present invention is as follows. After a substrate with 4H—SiC (0001) offset by 4° having an SiC epitaxial layer is oxidized for 30 minutes at 1150° C. in a thermal oxidation furnace, a hydrofluoric acid treatment is performed to make a surface clean. A through oxide film having a thickness of 10 nm is formed again in the thermal oxidation furnace in order to prevent contamination. It is implanted with impurities in the ion implantation system shown in FIG. 2 . An SiC substrate sample 26 is placed in the end station 201 . Implantation may be performed at room temperature, but from the viewpoint of maintaining crystallization, the sample temperature may be heated to 300° C.
- TMA tetramethyl aluminum
- An implantation depth is controlled by extraction energy between the ion source 21 and the end station 201 , and an amount of implantation is controlled by a quantity of ion current. (A combination of the energy and the quantity of current is called the “implantation schedule”, and this controls an implantation profile).
- the SiC substrate sample 26 implanted is treated by means of the hydrofluoric acid treatment to remove the through oxide film, and subsequently, it is annealed for activation.
- an ion implanted region 4 is formed in a manner that the Al impurities are implanted into the SiC epitaxial layer 2 as shown in FIG. 1B . That is, after sacrifice oxidation and the hydrofluoric acid treatment, a mask 3 of SiO 2 etc. is formed on the epitaxial layer of silicon carbide (SiC), and the aluminum ions to be impurities are implanted into the epitaxial layer 2 of silicon carbide (SiC) by the ion implantation system shown in FIG. 2 etc. to selectively form the impurity implanted region 4 (a well region or a contact region).
- TMA tetramethyl aluminum
- an aluminum target as a source may be excited by plasma to extract aluminum ions to implant using the extraction electrode and the analyzer tube.
- FIG. 3 is a cross-section view of a heat treatment apparatus for annealing.
- a heat treatment chamber 30 is formed of aluminum with the reflectance of an inner wall thereof being enhanced by a mirror finish, and it is a water-cooled aluminum chamber configured so that a cooling fluid can flow in a liquid flow channel 31 .
- This heat treatment chamber 31 can be evacuated of air to a vacuum of about 10 ⁇ 2 Pa, and also in an atmospheric state, a heat treatment can be conducted.
- Heating means 33 is included in a susceptor 32 , and a silicon carbide (SiC) substrate 34 to be subjected to a heat treatment is placed on the upper side of a substrate support on the upper side in FIG. 3 of the susceptor 32 .
- SiC silicon carbide
- the susceptor support on which upper surface the silicon carbide (SiC) substrate 34 is placed is provided with a sensor 35 as shown in FIG. 3 for detecting a heating temperature.
- the heating means 33 thermal electron generating means for heating for electron impact is shown in FIG. 3 , but in addition to it, an infrared lamp for heating an infrared lamp or a high frequency induction coil for high frequency induction heating etc. may be used.
- the inside of the susceptor 32 can be evacuated of air by evacuation means, such as a vacuum pump, provided separately from the one for the heat treatment chamber so that a vacuum is always maintained to be not greater than about 10 ⁇ 2 Pa.
- annealing for activation is carried out using the heat treatment apparatus as shown in FIG. 3 to activate ( FIG. 1C ).
- a p-type impurity in silicon carbide (SiC) compared to activation of an n-type impurity, it is necessary to anneal at a higher temperature, and (1) surface irregularity called the “step bunching” on a surface of silicon carbide (SiC), as shown in FIG. 4 , was generated thereby.
- step bunching surface irregularity
- a cap layer 6 of a carbonized film (Materials Science Forum Vols. 483-485 (2005) pp. 599-604, Y. Negoro, T. Kimoto and H. Matsunami), an Si film or an AlN film (Journal of Applied Physics Vol. 86 (1999) pp. 746-751, Evan M. Handy, Muluri V. Rao, K. A. Jones, M. A. Derenge, P. H. Chi, R. D.
- the aforementioned annealing method for activating the implanted impurities into the silicon carbide (SiC) substrate has a problem described below.
- the method in that the cap layer 6 of the carbonized film, the Si film, the AlN film or the like as shown in FIG. 1E is deposited on the surface of the silicon carbide (SiC) substrate has been proposed, but it increases the number of steps before and after, leading to an increase in a manufacturing cost. It was reported that, as shown in FIG. 1F , usage of the SiH 4 addition or the silicon carbide (SiC) vessel 34 ( FIG. 1F ) controls the surface irregularity, but a problem of repeatability or controllability has arisen.
- an internal part in an annealing apparatus a part which suppresses emission of a discharge gas is used, and in a vacuum, annealing is carried out, and whereby, possibility for controlling the surface irregularity has been found out, but, only under a reduced pressure condition, it is not sufficient in repeatability etc., dependent on implantation species or implantation conditions.
- the present inventors found out that, by evacuating the vacuum vessel in the end station 20 shown in FIG. 2 of air so that a pressure in the vacuum vessel is not greater than 10 ⁇ 5 Pa, setting a partial pressure of residual H 2 O in the vacuum vessel to be not greater than 10 ⁇ 2 Pa, and annealing (for example, at 1800° C.) under this condition, the surface flatness (RMS value) reached about 2 nm, which was considerably lower than 6 nm.
- activation ratio was about 80% and the RMS value was 0.8 nm, and so we achieved a high, electric activation while maintaining the surface flatness (RMS value) to be not greater than 1 nm. That is, it was found out that, under an atmosphere in which H 2 O is reduced as much as possible, if the high, electric activation is provided at a higher temperature, the surface flatness can be maintained.
- the “activation ratio” used herein is a ratio indicating how many carriers (electrons and holes) the implanted impurities create.
- annealing is performed at 1800° C.
- FIG. 5 is a graph illustrating relationship between the partial pressure of residual H 2 O and the surface irregularity. It will be seen from the graph in FIG. 5 that, in the atmosphere with the partial pressure of H 2 O of about 10 ⁇ 2 Pa, the surface flatness is controlled to be 2 nm, and in the atmosphere with the partial pressure of H 2 O of about 10 ⁇ 3 Pa, the surface flatness is controlled to be 1 nm.
- the high, electric activation can be easily accomplished while maintaining the surface flatness (RMS value) to be equal to or less than 2 nm, and preferably equal to or less than 1 nm in the end, because, by providing an atmosphere having the partial pressure of residual H 2 O which is not greater than 10 ⁇ 2 Pa or 10 ⁇ 3 Pa, the reaction probability between the silicon carbide (SiC) and the residual moisture can be largely reduced even at a high temperature, and the etching reaction can be suppressed.
- RMS value surface flatness
- a specific measuring method of the surface flatness (RMS) performed in the present invention is as follows.
- FIG. 6 is a cross-section view of another heat treatment apparatus 60 for implementing the annealing method of the present invention.
- FIGS. 7A to 7D are perspective views illustrating a covering body (cap) in FIG. 6 .
- the heat treatment apparatus shown in FIG. 6 differed from the heat treatment apparatus shown in FIG.
- a through-hole 65 an air vent communicating between a space 64 formed between the covering body (cap) 61 and a wall 62 of a heat treatment chamber, and a space 64 in the heat treatment chamber is formed in a peripheral wall 55 of the covering body (cap) 61 , and whereby, the conductance in the vicinity of a silicon carbide (SiC) substrate 63 to be subject to a heat treatment by heating means is increased.
- SiC silicon carbide
- a silicon carbide (SiC) substrate 63 can be more uniformly heated because of the covering body (cap) having such through-hole 65 , achieving sufficient activation.
- a cap 70 A in FIG. 7A includes a leg 70 A 2 under a cylindrical, peripheral wall of the cap 70 A, and a through-hole is formed between the legs.
- a cap 70 B in FIG. 7B includes a hole 70 B 2 drilled in a cylindrical, peripheral wall 70 B 1 of the cap, and the hole 70 B 2 forms a through-hole.
- a cap 70 C in FIG. 7C includes a hole 70 C 2 drilled in a cylindrical top plate 70 C 1 , and the hole 70 C 2 forms a through-hole.
- a cap 67 in FIG. 7D is cylindrically formed by a net 70 D 1 , and a mesh of the net forms a through-hole.
- an SiO 2 film etc. is deposited on the silicon carbide (SiC) substrate 81 , a mask 83 is formed by lithography and dry etching, and aluminum ions to be impurities are implanted using the ion implantation system shown in FIG. 2 etc. to selectively form the well region 82 in the silicon carbide (SiC) substrate 81 (see FIG. 8A ).
- TMA tetramethyl aluminum
- aluminum as a source may be excited by plasma to extract aluminum ions to implant using the extraction electrode and the analyzer tube and the ion implantation also may be carried out.
- annealing is carried out using the heat treatment apparatus as shown in FIG. 1D , FIG. 3 or FIG. 6 (see FIG. 8B ). In addition, in this embodiment, the annealing is performed at 1800° C., but the annealing also may be done at in the range of 1500° C. to 2300° C.
- FIG. 9A and FIG. 9B show a process flow of steps (a) to (p) for manufacturing a silicon carbide (SiC)-DMOSFET according to the present invention.
- step (a) an SiC substrate 91 having an SiC epitaxial layer formed thereon is provided.
- step (b) a pattern of an SiO 2 mask 92 to form two p-type wells is formed.
- step (c) Al ions are implanted into a p-type well 93 .
- step (d) the SiO 2 mask 92 is removed.
- a pattern of an SiO 2 mask 94 for a channel to be exposed between the two p-type wells is formed.
- step (f) N ions are implanted into the channel to form a channel 95 .
- step (g) the SiO 2 mask 94 for the channel is removed.
- step (h) an SiO 2 mask 96 to form an n + contact, exposing a part of the p-type well is formed.
- step (i) P ions are implanted into a contact region 97 to form an n + contact 97 .
- the SiO 2 mask 96 for the n + contact is removed.
- step (h) an SiO 2 mask 98 for a +p contact is formed to expose the n + contact region by the p-type well.
- step (l) Al ions are implanted into a p + contact region 99 to form a p + contact 99 .
- step (m) the SiO 2 mask 98 for the +p contact is removed.
- step (n) the impurity regions 93 , 95 , 97 , 99 formed in the SiC epitaxial layer of the SiC substrate are annealed for activation in the atmosphere described above according to the present invention.
- step (o) a gate oxide film 100 is formed on a surface of the SiC substrate after the annealing. With the annealing treatment according to the present invention, the gate oxide film does not lose reliability, and the channel mobility is prevented from being lowered while achieving a higher flatness on the surface.
- step (p) a source electrode 101 , a gate electrode 102 , a source electrode 103 and a drain electrode 104 are formed and a structure of the SiC-DMOSFET is completed.
- the “dose amount” used herein means an amount of addition of impurities implanted into a semiconductor substrate through the ion implantation, and it is determined by the ion beam energy and the time period of irradiation of the ion beam.
- the problems including reliability of a gate oxide film in a MOSFET is lowered, the channel mobility is reduced, or a leakage electric current in a p-n junction is increased, do not occur.
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Abstract
Description
- The present invention relates to an annealing method for activating an ion implanted region in a device including a silicon carbide (SiC) substrate having an ion implanted layer formed therein and a semiconductor device.
- When a semiconductor device such as a MOSFET (MOS Field-Effect Transistor) is manufactured, impurity control of a semiconductor substrate is necessary. For impurity control in using a silicon carbide (SiC) substrate, a combination of ion implantation and activation annealing process generally is used, because a diffusion rate of impurity is very small. (Phys. Stat. Sol. (a) Vol. 162 (1997), p, 263, T. Kimoto, N. Inoue and H. Matsunami). For the impurity control of a silicon carbide (SiC) semiconductor device, ions to provide impurities are implanted into a required part of the silicon carbide (SiC) substrate by an ion implantation system. Next, the silicon carbide (SiC) substrate is annealed to activate impurities using a high temperature annealing apparatus such as a high frequency induction heating apparatus. (See Japanese Patent Application Laid-Open No. 2004-311696)
- However, when annealing is performed to activate impurities in a silicon carbide (SiC) substrate, surface irregularity having a surface flatness of about 6.0 nm (RMS value) is generated, and it is observed that reliability of a gate insulating film and channel mobility were lowered in such semiconductor device. Therefore, the present invention aims to solve the problems described above, and to provide an annealing method for annealing a device including a silicon carbide (SiC) substrate so that the surface flatness (RMS value) is controlled to be not greater than 6.0 nm, and further to provide a semiconductor device in which a high, electric activation can be accomplished while maintaining the surface flatness (RMS value) to be not greater than 2 nm, and preferably not greater than 1 nm by using this annealing method.
- An annealing method for annealing a device including a silicon carbide (SiC) substrate according to the present invention includes a step of forming an impurity doped region in a silicon carbide (SiC) substrate and a step of annealing the impurity doped region in the silicon carbide (SiC) substrate, and it is specified that a partial pressure of H2O in an annealing atmosphere in the annealing step is not larger than 10−2 Pa.
- In one embodiment, the silicon carbide (SiC) substrate has an epitaxial silicon carbide (SiC) crystalline layer as a surface layer, and an impurity doped region is formed in the silicon carbide (SiC) crystalline layer.
- It is more preferable that an atmosphere for the annealing step has a partial pressure of H2O not larger than 10−3 Pa. In the annealing step, the silicon carbide (SiC) substrate implanted with impurities is preferably annealed with being covered by a cap.
- The annealing step is carried out in a vacuum vessel capable of evacuating of air, and in one embodiment, the vacuum vessel is evacuated of air so that a pressure in the vacuum vessel is not greater than 10−4 Pa. There is provided a semiconductor device including a silicon carbide (SiC) substrate and an impurity doped region in the substrate, in which a surface flatness of the silicon carbide (SiC) substrate is not greater than 2 nm, and more preferably not greater than 1 nm in RMS value, and in one embodiment, the semiconductor device is a MOS field-effect transistor.
- An annealing method for activating a device including a silicon carbide (SiC) substrate according to the present invention sets a partial pressure of residual H2O in a vacuum vessel to be not larger than 10−2 Pa, and anneals, and whereby, an advantage is provided that a surface flatness of the silicon carbide (SiC) substrate can be controlled to be equal to or less than 2 nm (RMS value). Further, by setting the partial pressure of residual H2O in the vacuum vessel to be not larger than 10−3 Pa and annealing, an advantage is provided that a semiconductor device can be provided in which a high, electric activation can be easily accomplished while maintaining the surface flatness to be equal to or less than 1 nm (RMS value).
-
FIG. 1A shows a silicon carbide (SiC) substrate having an epitaxial SiC layer; -
FIG. 1B shows impurity implantation into the silicon carbide (SiC) substrate shown inFIG. 1A ; -
FIG. 1C shows annealing of the silicon carbide (SiC) substrate implanted with impurities inFIG. 1B ; -
FIG. 1D shows an annealing heating apparatus using a cap; -
FIG. 1E shows annealing in which a cap layer is added; -
FIG. 1F shows an annealing heating apparatus using SiH4 addition and a vessel of silicon carbide; -
FIG. 2 schematically shows an ion implantation system; -
FIG. 3 is a cross-section view of a heating apparatus for annealing; -
FIG. 4 shows surface irregularity on a silicon carbide (SiC) substrate generated from annealing; -
FIG. 5 is a graph illustrating relationship between a partial pressure of residual H2O and the surface irregularity of a silicon carbide (SiC) substrate; -
FIG. 6 is a cross-section view of a heating apparatus using a cap having a through-hole for annealing; -
FIG. 7A shows a first example of a cap having a through-hole; -
FIG. 7B shows a second example of a cap having a through-hole; -
FIG. 7C shows a third example of a cap having a through-hole; -
FIG. 7D shows a fourth example of a cap having a through-hole; -
FIG. 8A shows impurity implantation into a silicon carbide (SiC) substrate; -
FIG. 8B shows annealing of the silicon carbide (SiC) substrate inFIG. 8A ; and -
FIG. 9A andFIG. 9B show a process flow for manufacturing a silicon carbide (SiC)-DMOSFET. -
FIGS. 1A to 1F are process drawings illustrating steps of an annealing method for activating a device including a silicon carbide (SiC) substrate implanted with aluminum as atoms for impurity ions. Generally, because the quality of a monocrystal silicon carbide (SiC) substrate is yet questionable, an epitaxial growth is conducted on a surface of the monocrystal SIC substrate in an SiC epitaxial growth furnace, and subsequently, in this SiC epitaxial layer, a device is formed. Because silicon carbide (SiC) has a plurality of crystalline types such as 3C, 4H and 6H, a silicon carbide (SiC) substrate of which crystalline orientation is offset relative to a surface of the C axis by 4° or 8° is used in order to conduct a homoepitaxial growth with a uniform crystalline orientation. (step flow growth: Ext. Abst. 19th Conf. Solid State Devices and Materials (Tokyo, 1987) 227, N. Kuroda, K. Shibahara, W. S. Yoo, S. Nishino and H. Matsunami) A step of growing anSiC epitaxial layer 2 on a monocrystal silicon carbide (SiC)substrate 1 shown inFIG. 1A will be described. A surface of the monocrystal SiC substrate is etched at a temperature of about 1300° C. using HCl (flow rate: 1 mL/min.), and a damaged layer is removed. Next, an epitaxial layer of silicon carbide (SiC) is grown (growth rate: 3 μm/hour) at a temperature of about 1500° C. using an SiH4 gas (50 sccm, 1.0% H2 dilution) and a C3H8 gas (33 sccm, 1.0% H2 dilution) as raw material gases, and an H2 gas (flow rate: 3 sLm) as a carrier gas. At this time, with flowing a nitrogen gas (6 sccm contained in 0.5% H2) as a doping gas, an n-type epitaxial layer is formed. According to the step described above, anepitaxial layer 2 of silicon carbide (SiC) (film thickness: 10 μm) is formed on the monocrystal silicon carbide (SiC)substrate 1. In addition, the monocrystal silicon carbide (SiC) substrate and also the entire structure in which the epitaxial SiC layer is formed on the monocrystal substrate shown inFIG. 1A may be herein called the “silicon carbide (SiC) substrate” collectively. -
FIG. 2 shows an ion implantation system for selectively forming a well region or a contact region for manufacturing a device on a SiC substrate. Operation of the ion implantation system used in the present invention is as follows. Impurity material desired to implant is ionized using a filament or plasma in anion source 21 in anion gun 20. Plasma (excited ion species) is extracted in a form of beam using anextraction electrode 22. Only impurity ions desired to implant are extracted using an analyzingmagnet 23 or an analyzer tube. Implantation energy is determined by an accelerating voltage between theion source 21 and an end station 201 at an acceleratingtube 24. (The implantation energy determines an implantation depth). Abeam 25 is scanned in order to uniformly implant the ions in a surface of awafer 26 having a mask in which an ion inflow region is exposed. In the end station 201, thewafer 26 may be rotated to improve uniformity, and it may be also heated to a high temperature to maintain crystallization. - An implantation process for implanting impurities into a SiC substrate used in the present invention is as follows. After a substrate with 4H—SiC (0001) offset by 4° having an SiC epitaxial layer is oxidized for 30 minutes at 1150° C. in a thermal oxidation furnace, a hydrofluoric acid treatment is performed to make a surface clean. A through oxide film having a thickness of 10 nm is formed again in the thermal oxidation furnace in order to prevent contamination. It is implanted with impurities in the ion implantation system shown in
FIG. 2 . AnSiC substrate sample 26 is placed in the end station 201. Implantation may be performed at room temperature, but from the viewpoint of maintaining crystallization, the sample temperature may be heated to 300° C. to 800° C. For the impurities, TMA (tetramethyl aluminum) as a source is excited by plasma to extract Al ions to implant using theextraction electrode 22 and the analyzingmagnet 23. An implantation depth is controlled by extraction energy between theion source 21 and the end station 201, and an amount of implantation is controlled by a quantity of ion current. (A combination of the energy and the quantity of current is called the “implantation schedule”, and this controls an implantation profile). TheSiC substrate sample 26 implanted is treated by means of the hydrofluoric acid treatment to remove the through oxide film, and subsequently, it is annealed for activation. - According to the process described above, an ion implanted
region 4 is formed in a manner that the Al impurities are implanted into theSiC epitaxial layer 2 as shown inFIG. 1B . That is, after sacrifice oxidation and the hydrofluoric acid treatment, amask 3 of SiO2 etc. is formed on the epitaxial layer of silicon carbide (SiC), and the aluminum ions to be impurities are implanted into theepitaxial layer 2 of silicon carbide (SiC) by the ion implantation system shown inFIG. 2 etc. to selectively form the impurity implanted region 4 (a well region or a contact region). In addition, in this embodiment, an example in which, for the impurities, TMA (tetramethyl aluminum) as a source is excited by plasma to extract Al ions to implant using the extraction electrode and the analyzer tube is described, alternatively, an aluminum target as a source may be excited by plasma to extract aluminum ions to implant using the extraction electrode and the analyzer tube. -
FIG. 3 is a cross-section view of a heat treatment apparatus for annealing. Aheat treatment chamber 30 is formed of aluminum with the reflectance of an inner wall thereof being enhanced by a mirror finish, and it is a water-cooled aluminum chamber configured so that a cooling fluid can flow in aliquid flow channel 31. Thisheat treatment chamber 31 can be evacuated of air to a vacuum of about 10−2 Pa, and also in an atmospheric state, a heat treatment can be conducted. Heating means 33 is included in asusceptor 32, and a silicon carbide (SiC)substrate 34 to be subjected to a heat treatment is placed on the upper side of a substrate support on the upper side inFIG. 3 of thesusceptor 32. On the susceptor support on which upper surface the silicon carbide (SiC)substrate 34 is placed is provided with asensor 35 as shown inFIG. 3 for detecting a heating temperature. As the heating means 33, thermal electron generating means for heating for electron impact is shown inFIG. 3 , but in addition to it, an infrared lamp for heating an infrared lamp or a high frequency induction coil for high frequency induction heating etc. may be used. The inside of thesusceptor 32 can be evacuated of air by evacuation means, such as a vacuum pump, provided separately from the one for the heat treatment chamber so that a vacuum is always maintained to be not greater than about 10−2 Pa. - Next, after removal of the mask, because the impurities implanted, as they are, are electrically inactive, annealing for activation is carried out using the heat treatment apparatus as shown in
FIG. 3 to activate (FIG. 1C ). Generally, for activating a p-type impurity in silicon carbide (SiC), compared to activation of an n-type impurity, it is necessary to anneal at a higher temperature, and (1) surface irregularity called the “step bunching” on a surface of silicon carbide (SiC), as shown inFIG. 4 , was generated thereby. To prevent it, in a conventional art, in annealing, as shown inFIG. 1D (see WO 2006/043530), after a substrate surface of the SiC substrate on the substrate support of thesusceptor 32 in the heat treatment apparatus is covered with a cap, annealing is sometimes performed. (2) Alternatively, as another way, as shown inFIG. 1E , acap layer 6 of a carbonized film (Materials Science Forum Vols. 483-485 (2005) pp. 599-604, Y. Negoro, T. Kimoto and H. Matsunami), an Si film or an AlN film (Journal of Applied Physics Vol. 86 (1999) pp. 746-751, Evan M. Handy, Muluri V. Rao, K. A. Jones, M. A. Derenge, P. H. Chi, R. D. Vispute, T. Venkatesan, N. A. Papanicolaou and J. Mittereder) is deposited on anepitaxial layer 3, and annealing is sometimes performed with theepitaxial layer 3 being covered. (3) Alternatively, as still another way, as shown inFIG. 1F , using addition of SiH4 (MRS Spring (2004), S. Rao, S. E. Saddow, F. Bergamini, R. Nipoti, Y. Emirov and A. Agarwal) or a silicon carbide (SiC) vessel (Materials Science Forum Vols. 483-485 (2005) pp. 621-624, M. Rambach, A. J. Bauer, L. Frey, P. Friedrichs and H. Ryssel), annealing is sometimes performed. - However, the aforementioned annealing method for activating the implanted impurities into the silicon carbide (SiC) substrate has a problem described below. The method in that the
cap layer 6 of the carbonized film, the Si film, the AlN film or the like as shown inFIG. 1E is deposited on the surface of the silicon carbide (SiC) substrate has been proposed, but it increases the number of steps before and after, leading to an increase in a manufacturing cost. It was reported that, as shown inFIG. 1F , usage of the SiH4 addition or the silicon carbide (SiC) vessel 34 (FIG. 1F ) controls the surface irregularity, but a problem of repeatability or controllability has arisen. Further, for an internal part in an annealing apparatus, a part which suppresses emission of a discharge gas is used, and in a vacuum, annealing is carried out, and whereby, possibility for controlling the surface irregularity has been found out, but, only under a reduced pressure condition, it is not sufficient in repeatability etc., dependent on implantation species or implantation conditions. - The present inventors found out that, by evacuating the vacuum vessel in the
end station 20 shown inFIG. 2 of air so that a pressure in the vacuum vessel is not greater than 10−5 Pa, setting a partial pressure of residual H2O in the vacuum vessel to be not greater than 10−2 Pa, and annealing (for example, at 1800° C.) under this condition, the surface flatness (RMS value) reached about 2 nm, which was considerably lower than 6 nm. Further, by setting the partial pressure of residual H2O in the vacuum vessel to be not greater than 10−3 Pa and annealing (for example, 1800° C.) under this condition, activation ratio was about 80% and the RMS value was 0.8 nm, and so we achieved a high, electric activation while maintaining the surface flatness (RMS value) to be not greater than 1 nm. That is, it was found out that, under an atmosphere in which H2O is reduced as much as possible, if the high, electric activation is provided at a higher temperature, the surface flatness can be maintained. In addition, the “activation ratio” used herein is a ratio indicating how many carriers (electrons and holes) the implanted impurities create. Further, in this embodiment, an example in which annealing is performed at 1800° C. is described, but the annealing also may be done at in the range of 1500° C. to 2200° C. It is thought that, in the annealing at a temperature higher than 1500° C., the surface is etched in the etching reaction of 2H2O+SiC=>SiO↑+CO↑+2H2↑, and even if a high purity Ar gas of 5N is used in an Ar atmosphere, the partial pressure of H2O is about 1 Pa, so that reaction probability as described above is higher by a factor of 1000, as a result, the surface is roughened. -
FIG. 5 is a graph illustrating relationship between the partial pressure of residual H2O and the surface irregularity. It will be seen from the graph inFIG. 5 that, in the atmosphere with the partial pressure of H2O of about 10−2 Pa, the surface flatness is controlled to be 2 nm, and in the atmosphere with the partial pressure of H2O of about 10−3 Pa, the surface flatness is controlled to be 1 nm. In addition, it was found out that, also in the annealing in the atmosphere having the high purity Ar gas introduced therein or in the annealing in a reduced pressure, the surface irregularity was some improved, but the surface was etched due to reaction between the silicon carbide (SiC) substrate and residual moisture at a high temperature, and roughened, and therefore, the surface flatness (RMS value)<2 nm, or <1 nm was not achieved. In the present invention, the high, electric activation can be easily accomplished while maintaining the surface flatness (RMS value) to be equal to or less than 2 nm, and preferably equal to or less than 1 nm in the end, because, by providing an atmosphere having the partial pressure of residual H2O which is not greater than 10−2 Pa or 10−3 Pa, the reaction probability between the silicon carbide (SiC) and the residual moisture can be largely reduced even at a high temperature, and the etching reaction can be suppressed. - In addition, a specific measuring method of the surface flatness (RMS) performed in the present invention is as follows.
- 1. Measurement equipment: AFM (Atomic Force Microscopy)
-
- Name of the maker: SII (Seiko Instruments Inc.)
- 2. Type name: NPX200M0001
-
- Viewing head: NPX200
- Controller: Nanopics 2100
- 3. Measuring method
-
- Scanning in DFM (Damping Force Mode)
- (The mode in that a probe oscillating periodically at a constant amplitude is brought near a surface of a silicon carbide (SiC) substrate sample and a distance from a cantilever to the surface of the sample is controlled to keep the attenuation of the amplitude to be constant)
- 4. Measurement region: 4×4 μm2.
-
FIG. 6 is a cross-section view of anotherheat treatment apparatus 60 for implementing the annealing method of the present invention.FIGS. 7A to 7D are perspective views illustrating a covering body (cap) inFIG. 6 . In the heat treatment apparatus shown inFIG. 6 , differed from the heat treatment apparatus shown inFIG. 1D (see WO 2006/043530), a through-hole 65, an air vent communicating between aspace 64 formed between the covering body (cap) 61 and awall 62 of a heat treatment chamber, and aspace 64 in the heat treatment chamber is formed in a peripheral wall 55 of the covering body (cap) 61, and whereby, the conductance in the vicinity of a silicon carbide (SiC)substrate 63 to be subject to a heat treatment by heating means is increased. - Therefore, in an atmosphere in which the partial pressure of residual H2O in the heat treatment chamber is controlled to be not greater than 10−2 Pa, and preferably not greater than 10−3 Pa, by evacuating with a vacuum pump the heat treatment chamber shown in
FIG. 6 of air so that a pressure in the heat treatment chamber is not greater than 10−5 Pa, a silicon carbide (SiC)substrate 63 can be more uniformly heated because of the covering body (cap) having such through-hole 65, achieving sufficient activation. - A
cap 70A inFIG. 7A includes a leg 70A2 under a cylindrical, peripheral wall of thecap 70A, and a through-hole is formed between the legs. Acap 70B inFIG. 7B includes a hole 70B2 drilled in a cylindrical, peripheral wall 70B1 of the cap, and the hole 70B2 forms a through-hole. Acap 70C inFIG. 7C includes a hole 70C2 drilled in a cylindrical top plate 70C1, and the hole 70C2 forms a through-hole. Acap 67 inFIG. 7D is cylindrically formed by a net 70D1, and a mesh of the net forms a through-hole. Next, referring toFIGS. 8A and 8B , an annealing method for annealing awell region 82 implanted with impurities of a silicon carbide (SiC)substrate 81 will be described. - After the sacrifice oxidation and the hydrofluoric acid treatment, an SiO2 film etc. is deposited on the silicon carbide (SiC)
substrate 81, amask 83 is formed by lithography and dry etching, and aluminum ions to be impurities are implanted using the ion implantation system shown inFIG. 2 etc. to selectively form thewell region 82 in the silicon carbide (SiC) substrate 81 (seeFIG. 8A ). In addition, in this embodiment, for the impurities, TMA (tetramethyl aluminum) as a source is excited by plasma to extract Al ions to implant using the extraction electrode and the analyzer tube and the ion implantation is carried out, alternatively, aluminum as a source may be excited by plasma to extract aluminum ions to implant using the extraction electrode and the analyzer tube and the ion implantation also may be carried out. After removal of a mask, to activate the well region, annealing is carried out using the heat treatment apparatus as shown inFIG. 1D ,FIG. 3 orFIG. 6 (seeFIG. 8B ). In addition, in this embodiment, the annealing is performed at 1800° C., but the annealing also may be done at in the range of 1500° C. to 2300° C. -
FIG. 9A andFIG. 9B show a process flow of steps (a) to (p) for manufacturing a silicon carbide (SiC)-DMOSFET according to the present invention. In step (a), anSiC substrate 91 having an SiC epitaxial layer formed thereon is provided. In step (b), a pattern of an SiO2 mask 92 to form two p-type wells is formed. In step (c), Al ions are implanted into a p-type well 93. In step (d), the SiO2 mask 92 is removed. In step (e), a pattern of an SiO2 mask 94 for a channel to be exposed between the two p-type wells is formed. In step (f), N ions are implanted into the channel to form achannel 95. In step (g), the SiO2 mask 94 for the channel is removed. In step (h), an SiO2 mask 96 to form an n+ contact, exposing a part of the p-type well is formed. - In step (i), P ions are implanted into a
contact region 97 to form an n+ contact 97. In step (j), the SiO2 mask 96 for the n+ contact is removed. In step (h), an SiO2 mask 98 for a +p contact is formed to expose the n+ contact region by the p-type well. In step (l), Al ions are implanted into a p+ contact region 99 to form a p+ contact 99. In step (m), the SiO2 mask 98 for the +p contact is removed. In step (n), theimpurity regions gate oxide film 100 is formed on a surface of the SiC substrate after the annealing. With the annealing treatment according to the present invention, the gate oxide film does not lose reliability, and the channel mobility is prevented from being lowered while achieving a higher flatness on the surface. Finally, in step (p), asource electrode 101, agate electrode 102, asource electrode 103 and adrain electrode 104 are formed and a structure of the SiC-DMOSFET is completed. - In addition, the “dose amount” used herein means an amount of addition of impurities implanted into a semiconductor substrate through the ion implantation, and it is determined by the ion beam energy and the time period of irradiation of the ion beam. By applying the process flow to formation of the n+ contact region implanted with phosphorus (P) or nitrogen (N) and the channel region, besides formation of the p-type well region and the p+ contact region, a silicon carbide (SiC) MOSFET as shown in
FIG. 9 can be manufactured. Also, when the RMS value reaches 0.6 nm, the problems, including reliability of a gate oxide film in a MOSFET is lowered, the channel mobility is reduced, or a leakage electric current in a p-n junction is increased, do not occur.
Claims (8)
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CN101652835A (en) | 2010-02-17 |
US20110121317A1 (en) | 2011-05-26 |
US8198182B2 (en) | 2012-06-12 |
WO2008136126A1 (en) | 2008-11-13 |
CN101652835B (en) | 2012-03-21 |
JPWO2008136126A1 (en) | 2010-07-29 |
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