The present invention relates to a silicon carbide semiconductor device, and more particularly, to a silicon carbide semiconductor device having an ohmic electrode.
The silicon carbide semiconductor device such as an FET (field effect transistor) using silicon carbide (SiC) is conventionally known (for example, see “Semiconductor SiC Technology and Applications”, page 191 (Non-Patent Document 1)). For example, while an MOSFET (Metal-Oxide-Semiconductor Field-Effect Transistor) using SiC is a unipolar device, a high reverse breakdown voltage (for example, 1 kV or more) that is achieved only by a bipolar transistor device such as a GTO (Gate Turn-Off thyristor) and an IGBT (Insulated Gate Bipolar Transistor) can be achieved in the case of the device using Si. Accordingly, such a device is expected to serve as a device that allows a high reverse breakdown voltage, low loss and fast switching. In addition, the MOSFET as a power device using Si is generally configured to employ a DMOSFET (Double-Diffused-MOSFET) structure. In the case of the MOSFET using SiC, conductive impurities are selectively doped by ion implantation. Thus, the MOSFET having conductive impurities implanted thereinto by such ion implantation is referred to as a DiMOSFET (Double-Implanted MOSFET).
In the above-described MOSFET, an epitaxial layer made of SiC is formed on the surface of an SiC substrate, for example, having n type conductivity. Then, p type conductive impurities are ion-implanted into this epitaxial layer to form a p type region. Consequently, a p type ohmic electrode is formed so as to be in contact with the p type region.
In order to lower the contact resistance between the p type region and the ohmic electrode, it is conceivable to increase the concentration of the p type conductive impurities in the p type region (that is, increase the amount of the conductive impurities to be implanted). In this case, however, a lot of defects caused by ion implantation are formed in the p type region. These defects may act as a leak path of electric current, which causes deterioration of the reverse breakdown voltage performance of the MOSFET. Thus, in the semiconductor device using SiC, it is conventionally difficult to lower the contact resistance between the ohmic electrode and the impurity region while achieving high reverse breakdown voltage characteristics. The present invention has been made to solve the above-described problems, and an object of the present invention is to provide a silicon carbide semiconductor device capable of lowering the contact resistance of the ohmic electrode while achieving high reverse breakdown voltage characteristics.
The silicon carbide semiconductor device according to the present invention includes a substrate and an impurity layer. The substrate having a first conductive type is made of silicon carbide and has a dislocation density of 5×103 cm−2 or less. The impurity layer is formed on the substrate, in which a concentration of conductive impurities having a second conductive type different from the first conductive type is 1×1020 cm3 or more and 5×1021 cm−3 or less.
Thus, when an ohmic electrode is formed so as to be in contact with the impurity layer, the contact resistance between the ohmic electrode and the impurity layer can be lowered to the level at which there is no problem from a practical standpoint. In addition, the substrate having a dislocation density lowered to the above-mentioned value is used, thereby sufficiently lowering the density of the defects that may lead to a leak path in the substrate and in the impurity layer formed on the substrate. Consequently, the reverse breakdown voltage characteristics of the silicon carbide semiconductor device can be better.
The dislocation density of the substrate is set at 5×103 cm−2 or less since this allows the reverse breakdown voltage characteristics of the silicon carbide semiconductor device to be well maintained. Furthermore, the lower limit of the conductive impurity concentration in the impurity layer is set at 1×1020 cm−3. This is because the conductive impurity concentration lower than this value may cause the contact resistance between the ohmic electrode and the impurity layer to be increased beyond the allowable range when the ohmic electrode is formed so as to be in contact with the impurity layer. Furthermore, the upper limit of the conductive impurity concentration in the impurity layer is set at 5×1021 cm−3 since implantation of the conductive impurities beyond this upper limit may lead to deterioration of the crystallinity of the impurity layer. Consequently, the characteristics of the silicon carbide semiconductor device may be deteriorated.
As described above, the present invention can provide a silicon carbide semiconductor device having excellent reverse breakdown voltage characteristics while capable of lowering the contact resistance of the ohmic electrode to the level at which there is no problem from a practical standpoint.
The embodiments of the present invention will be hereinafter described with reference to the drawings, in which the same or corresponding components are designated by the same reference characters, and description thereof will not be repeated.
Referring to
Referring to
Reverse breakdown voltage holding layer 22 has a surface on which p regions 23 of p type conductivity are formed spaced apart from each other. The concentration of the p type conductive impurities in p region 23 may be set, for example, at 1×1017 cm−3. Within p region 23, n+ region 24 is formed on the surface layer of p region 23. The concentration of the n type conductive impurities in n+ region 24 may be set, for example, at 1×1019 cm−3. Furthermore, p+ region 25 is formed in the position adjacent to n+ region 24. The concentration of the p type conductive impurities in n+ region 25 may be set, for example, at 1×1020 cm−3. Oxide film 26 is formed so as to extend to cover the area from n+ region 24 in one p region 23 through the one p region 23, reverse breakdown voltage holding layer 22 exposed between two p regions 23, and the other p region 23 to n+ region 24 in the other p region 23. Gate electrode 10 is formed on oxide film 26. Furthermore, source electrode 11 is formed on n+ region 24 and p+ region 25. Upper source electrode 27 is formed on source electrode 11. In addition, drain electrode 12 is formed on the backside of substrate 2 opposite to the surface on which buffer layer 21 is formed.
In this case, the above-described semiconductor device 1 includes substrate 2 and p+ region 25 as an impurity layer. Substrate 2 is made of silicon carbide, has a dislocation density of 5×103 cm−2 or less and has the first conductive type (n type). Furthermore, p+ region 25 is formed on the substrate, in which the concentration of the conductive impurities having the second conductive type different from the first conductive type is 1×1020 cm−or more and 5×1021 cm−3 or less. Thus, in the case where source electrode 11 serving as an ohmic electrode is formed so as to be in contact with p+ region 25, the contact resistance between source electrode 11 and p+ region 25 can be lowered to the level at which there is no problem from a practical standpoint. Furthermore, substrate 2 having a dislocation density lowered to the above-described value is used to allow a sufficient decrease in the density of the defects which may lead to a leak path in substrate 2 and the epitaxial layer and the like formed on the substrate. Accordingly, excellent reverse breakdown voltage characteristics of semiconductor device 1 can be achieved.
In addition, the dislocation density of substrate 2 can be measured by etching the surface of substrate 2 using a chemical solution such as KOH, and counting the number of etch pits produced by this etching process. Furthermore, the concentration of the conductive impurities in p+ region 25 can be measured, for example, using an SIMS (Secondary Ionization Mass Spectrometer) and the like. When the (0001) Si plane or (0001) Si slightly tilted plane of substrate 2 made of silicon carbide is etched, the above-mentioned etch pits are formed due to screw dislocation (Burgers vector: 1 unit cell size in the c-axis direction), edge dislocation (Burgers vector: 1/3[11-20]), basal plane dislocation (Burgers vector: 1/3[11-20]), or the like.
Then, the operation of semiconductor device 1 shown in
The method of manufacturing semiconductor device 1 shown in
First, as shown in
Then, the buffer layer forming step (S20) is carried out. Specifically, an epitaxial layer made of silicon carbide having n type conductivity is formed as a buffer layer. It is to be noted that this buffer layer forming step (S20) may not be carried out, but the epitaxial layer forming step (S30) described below may be carried out subsequent to the above-described step (S10).
Then, the epitaxial layer forming step (S30) is carried out. Specifically, reverse breakdown voltage holding layer 22 is formed on buffer layer 21. Reverse breakdown voltage holding layer 22 is formed by the epitaxial growth method as a layer made of silicon carbide having n type conductivity. In this epitaxial layer forming step (S30), for example, SiH4 gas and C3H8 gas can be used as source gas.
Then, the implantation step (S40) is carried out. Specifically, the oxide film formed using photolithography and etching is used as a mask to implant the impurities of p type conductivity into reverse breakdown voltage holding layer 22. In this way, p region 23 (see
After the implantation step (S40) as described above, the activation heat treatment is performed. This activation heat treatment may be performed, for example, on the conditions that argon gas is used as atmospheric gas, the heating temperature is set at 1700° C. and the heating time period is 30 minutes.
Then, as shown in
Then, the electrode forming step (S60) is carried out. Specifically, a resist film having a pattern is formed on the oxide film using photolithography. The resist film is used as a mask to remove a portion of the oxide film located on n+ region 24 and p+ region 25 by etching. Then, a conductor film made of metal and the like is formed so as to be in contact with n+ region 24 and p+ region 25 within the opening provided on the resist film and in the oxide film. The resist film is then removed to remove (lift off) the conductor film located on the resist film.
In this case, for example, nickel (Ni) may be used for a material of the conductor film. Furthermore, the material to be used may include titanium (Ti), aluminum (Al), and a material containing silicon (Si) in these metals. Consequently, source electrode 11 can be obtained as shown in
Upper source electrode 27 (see
Referring to
Referring to
In second p type layer 34 and n type layer 33, source region 35 and drain region 37 are formed that contain impurities of n type conductivity (n type impurities) which are higher in concentration than those of n type layer 33. Furthermore, in second p type layer 34 and n type layer 33, gate region 36 is formed such that it is sandwiched between the above-described source region 35 and drain region 37, in which case gate region 36 contains impurities of p type conductivity (p type impurities) which are higher in concentration than those of each of first p type layer 32 and second p type layer 34. Thus, source region 35, gate region 36 and drain region 37 are formed so as to extend through second p type layer 34 to n type layer 33. Furthermore, the bottom of each of source region 35, gate region 36 and drain region 37 is located spaced apart from the upper surface of first p type layer 32 (boundary area between first p type layer 32 and n type layer 33).
Furthermore, on the side opposite to gate region 36 with respect to source region 35, a groove 41 is provided so as to extend from an upper surface 34A of second p type layer 34 (the main surface on the side opposite to the surface facing n type layer 33) through second p type layer 34 to n type layer 33. The bottom wall of groove 41 is located within n type layer 33 and spaced apart from the interface between first p type layer 32 and n type layer 33. Furthermore, potential holding region 43 is formed so as to extend from the bottom wall of groove 41 through n type layer 33 to first p type layer 32, in which case potential holding region 43 contains p type impurities which are higher in concentration than those of first p type layer 32 and second p type layer 34. The bottom of this potential holding region 43 is located spaced apart from the upper surface of n type substrate 2 (the boundary area between substrate 2 and first p type layer 32).
Contact electrode 39 is formed so as to be in contact with the upper surface of each of source region 35, gate region 36, drain region 37, and potential holding region 43. Contact electrode 39 is made of material that allows ohmic contact with source region 35, gate region 36, drain region 37, and potential holding region 43. A contact electrode 19 may be made of Ni, for example. Furthermore, contact electrode 19 may be made of Ti, Al, or silicide of these metals.
Oxide film 38 is formed between contact electrodes 39 adjacent to each other. In other words, oxide film 38 serving as an insulating layer is formed on the upper surface of second p type layer 34 and the bottom wall and the sidewall of groove 41 so as to cover the entire region other than the region where contact electrode 39 is formed. Consequently, adjoining contact electrodes 19 are insulated from each other.
Upper source electrode 27, upper gate electrode 28 and upper drain electrode 29 are formed so as to be in contact with the upper surface of each contact electrode 39 located on source region 35, gate region 36 and drain region 37, respectively. Consequently, upper source electrode 27, upper gate electrode 28 and upper drain electrode 29 are electrically connected through contact electrode 39 to source region 35, gate region 36 and drain region 37, respectively. Furthermore, upper source electrode 27 is formed so as to extend from the upper surface of contact electrode 19 on source region 35 to the upper surface of contact electrode 19 on potential holding region 43. Consequently, contact electrode 39 on potential holding region 43 is maintained at the same electric potential as that of contact electrode 39 on source region 35. Upper source electrode 27, upper gate electrode 28 and upper drain electrode 29 each are made of a conductor such as Al, for example.
Semiconductor device 1 shown in
In this way, as in the case of semiconductor device 1 shown in the first embodiment, when contact electrode 39 serving as an ohmic electrode is formed so as to be in contact with gate region 36 serving as an impurity layer, the contact resistance between contact electrode 39 and gate region 36 can be lowered to the level at which there is no problem from a practical standpoint. Furthermore, substrate 2 having a dislocation density lowered to the above-mentioned value is used, which allows a sufficient decrease in the density of the defects that may lead to a leak path in substrate 2 and the epitaxial layer (first p type layer 32, n type layer 33 and second p type layer 34) formed on the substrate. Accordingly, the reverse breakdown voltage characteristics of semiconductor device 1 can be better.
Then, the operation of semiconductor device 1 will be briefly described. Referring to
In addition, when a negative voltage is applied to upper gate electrode 28, depletion in the above-described channel region and drift region is developed. This results in the state where source region 35 and drain region 37 are electrically interrupted. Accordingly, electrons cannot move from source region 35 toward drain region 37, which prevents the current from flowing.
Then, the manufacturing method of the semiconductor device shown in
As shown in
As shown in
Then, a groove is formed in second p type layer 34 and n type layer 33 formed as described above. Specifically, for example, dry etching is used to form groove 41 so as to extend from upper surface 34A of second p type layer 34 through second p type layer 34 to n type layer 33. In this step of forming groove 41, for example, a mask layer having an opening in the position where groove 41 is to be formed may be formed on upper surface 34A of second p type layer 34, and this mask layer may be used as a mask for dry etching using SF6 gas.
Then, the implantation step (S40) is carried out as shown in
Then, the second ion implantation step is carried out as an implantation step (S40). Specifically, as in the above-described first ion implantation step, the photolithography method is used to form a resist film having an opening in the region in accordance with the desired planar shape of each of gate region 36 and potential holding region 43. Then, this resist film is used as a mask to introduce p type impurities such as aluminum (Al) or boron (B) into the predetermined region of each of second p type layer 34, n type layer 33 and first p type layer 32 by the ion implantation method. Consequently, gate region 36 and potential holding region 43 are formed.
Then, the activation annealing step for activating the implanted n type impurities or p type impurities is carried out. In this activation annealing step, removal of the resist film used in the above-described implantation step (S40) is followed by heating of second p type layer 34, n type layer 33 and first p type layer 32 into which ions are implanted. Consequently, the impurities introduced by the above-described ion implantation are activated. The activation annealing treatment may be performed, for example, on the conditions that argon gas is used as an atmosphere, the heating temperature is set at about 1700° C. and the holding time period is about 30 minutes.
Then, the insulating film forming step (S70) is carried out as shown in
In this step (S70), the above-described step is carried out, to thereby cause thermal oxidization of the surface of substrate 2 on which second p type layer 34, n type layer 33 and first p type layer 32 are formed, each having a prescribed ion implantation layer formed therein. Accordingly, oxide film 38 made of silicon dioxide (SiO2) is formed so as to cover upper surface 34A of second p type layer 34 and the inner wall of groove 41.
The electrode forming step (S60) is then carried out as shown in
Then, a preferable variation of the semiconductor device shown in the above-described first and second embodiments will be described.
In the above-described semiconductor device 1, substrate 2 may have a dislocation density of 1×103 cm−2 or less. In this case, the reverse breakdown voltage characteristics of semiconductor device 1 can be much better.
In the above-described semiconductor device 1, substrate 2 may have a screw dislocation density of 1 cm−2 or less. In this case, since the screw dislocation in substrate 2 may lead to deterioration of the reverse breakdown voltage characteristics (may cause a decrease in the avalanche breakdown voltage), it is particularly effective to decrease the density. In this case, the upper limit of the screw dislocation density of substrate 2 is set at 1 cm−2. This is because the screw dislocation density exceeding this upper limit value may lead to deterioration of the reverse breakdown voltage.
In the above-described semiconductor device 1, substrate 2 may have a screw dislocation density of 0.1 cm2 or less. In this case, the reverse breakdown voltage characteristics of semiconductor device 1 can be much better. The more preferable upper limit of the screw dislocation density of substrate 2 is set at 0.1 cm−2. This is because this upper limit value set as described above reliably allows improvement in the reverse breakdown voltage.
In the above-described semiconductor device 1, the concentration of the second (p type) conductive impurities in p+ region 25 or gate region 36 as an impurity layer may be 4×1020 cm− or more and 5×1021 cm−3 or less. In this case, when source electrode 11 or contact electrode 39 serving as an ohmic electrode is formed so as to be in contact with the impurity layer, the contact resistance between source electrode 11 and p+ region 25 or between contact electrode 39 and gate region 36 can be further lowered. The more preferable lower limit of the concentration of the conductive impurities is set at 4×1020 cm−3 because this lower limit allows the contact resistance to be further lowered. Furthermore, the more preferable upper limit of the concentration of the conductive impurities is set at 5×1021 cm−3. This is because when the conductive impurities are introduced beyond this upper limit, the crystallinity of the impurity layer may be degraded, which leads to deterioration of the characteristics of the silicon carbide semiconductor device. The above-described semiconductor device 1 may include an ohmic electrode (source electrode 11) formed so as to be in contact with the impurity layer (p+ region 25) and another ohmic electrode (drain electrode 12) formed so as to be in contact with substrate 2. Source electrode 11 and drain electrode 12 may be made of the same material. In this case, since the above-described source electrode 11 and drain electrode 12 can be formed using the same material, source electrode 11 and drain electrode 12 can be simultaneously or sequentially formed. Accordingly, the manufacturing process of semiconductor device 1 can be simplified as compared with the case where source electrode 11 and drain electrode 12 are made of different materials.
In the above-described semiconductor device 1, the material forming source electrode 11 and drain electrode 12 may include nickel (Ni). In this case, the material containing nickel is employed to form source electrode 11 and drain electrode 12 which are in contact with the impurity layer (p+ region 25) and substrate 2, respectively, which are different in conductive type. Consequently, the same material can be used to form the electrodes (source electrode 11 and drain electrode 12) which are in ohmic contact with the impurity layer (p+ region 25) and substrate 2.
In the above-described semiconductor device 1, the material forming each of source electrode 11 and drain electrode 12 may include titanium (Ti) and aluminum (Al). Furthermore, in the above-described semiconductor device 1, the material forming source electrode 11 and drain electrode 12 may include silicon (Si) in addition to titanium and aluminum. In this case, the same material can be used to form the electrodes (source electrode 11 and drain electrode 12) which are in ohmic contact with the impurity layer (p+ region 25) and substrate 2, respectively, which are different in conductive type.
In the above-described semiconductor device 1, the material forming the above-described source electrode 11 and drain electrode 12 or contact electrode 39 may include a stacking structure of titanium, aluminum and silicon. In this case, for example, the thickness of titanium may be 0 nm or more and 40 nm or less, the thickness of aluminum may be 20 nm or more and 100 nm or less, and the thickness of silicon may be 10 nm or more and 50 nm or less. More preferably, the thickness of titanium may be 5 nm or more and 30 nm or less, the thickness of aluminum may be 30 nm or more and 70 nm or less, and the thickness of silicon may be 15 nm or more and 35 nm or less.
The following experiments were conducted in order to confirm the effects of the present invention.
[Sample]
Sample of Inventive Example:
As shown in
Substrate 2 made of silicon carbide was prepared. This substrate 2 had a (0001) plane having an off angle of 8 degrees in the <11-20>direction. The dislocation density of substrate 2 was 1×103 cm−2. The concentration of the n type conductive impurities in buffer layer 21 was 5×1017 cm−3. Nitrogen was used as n type conductive impurities. Furthermore, buffer layer 21 was configured to have a thickness of 0.5 μm.
Furthermore, the concentration of the n type conductive impurities in n− type layer 52 was set at 5×1015 cm−3. The thickness of n type layer 52 was 2.2 μm. It is to be noted that elements similar to those of the above-described buffer layer 21 were used for n type conductive impurities in n− type layer 52. Furthermore, the concentration profile of the conductive impurities in p type layer 53 and p+ type layer 54 is as shown in
Referring to
Sample of Comparative Example:
For the sample of the comparative example, a substrate having a similar structure but having a dislocation density in substrate 2 of 1×104 cm2 was used. Other structures are similar to those of the sample of the inventive example shown in
Sample of Comparative Example 2:
The sample of Comparative Example 2 is also similar in structure to the semiconductor device shown in
[Measurement]
With regard to the samples of the above-described inventive example and Comparative Examples 1 and 2, the contact resistance between ohmic electrode 55 and p+ type layer 54 as well as the current-voltage characteristics in the reverse direction for the formed samples were measured. The TLM (Transmission Line Model) method was used as a method for measuring the contact resistance. Furthermore, the method of current-voltage characteristics measurement by a curve tracer was used as a method for measuring the current-voltage characteristics in the reverse direction.
[Results]
The measurement results of the inventive example are shown in
As can be seen from
Then, the measurement results of Comparative Example 1 are shown in
As for the sample of Comparative Example 2, the current-voltage characteristics in the reverse direction are the same as those of the sample of Comparative Example 1, and a leakage current was detected from the relatively low voltage. Furthermore, in the sample of Comparative Example 2, the contact resistance of the ohmic electrode was 2×10−2 Ωcm−2 which was greater than the contact resistance of the sample of each of Example 2 and Comparative Example 1.
The following experiments were conducted in order to confirm the relationship between the reverse breakdown voltage and the dislocation density of the substrate in the present invention.
[Sample]
As in Example 1, the samples each having the structure shown in
[Measurement]
The method similar to that in Example 1 was employed to measure the current-voltage characteristics in the reverse direction for each sample. Then, the voltage at the time when the flowed current (leakage current) exceeded 10 μA was defined as a reverse breakdown voltage, to determine the value of the reverse breakdown voltage for each sample.
[Results]
The measurement results are shown in
The following experiments were conducted in order to confirm the relationship between the contact resistance of the ohmic electrode and the concentration of the conductive impurities of the impurity layer formed so as to be in contact with the ohmic electrode, in accordance with the present invention.
[Sample]
As in the inventive example of Example 1, the samples each having the structure shown in
[Measurement]
The method similar to that in Example 1 was employed to measure the contact resistance between ohmic electrode 55 and p+ type layer 54 for each sample.
[Results]
As can be seen from
It should be understood that the embodiments and examples disclosed herein are illustrative and non-restrictive in every respect. The scope of the present invention is defined by the terms of the claims, rather than the description above, and is intended to include any modifications within the scope and meaning equivalent to the terms of the claims.
The present invention can be applied to a silicon carbide semiconductor device having an ohmic electrode, and particularly, is advantageously applied to a DiMOSFET, a JFET, and the like.
1 semiconductor device, 2 substrate, 10 gate electrode, 11 source electrode, 12 drain electrode, 19 contact electrode, 21, 51 buffer layer, 22 reverse breakdown voltage holding layer, 23 p region, 24 n+ region, 25 p+ region, 26, 38 oxide film, 27 upper source electrode, 28 upper gate electrode, 29 upper drain electrode, 32 first p type layer, 33 n type layer, 34 second p type layer, 34A upper surface, 35 source region, 36 gate region, 37 drain region, 39 contact electrode, 41 groove, 43 potential holding region, 52 n− type layer, 53 p type layer, 54 p+ type layer, 55 ohmic electrode, 56 electrode, 57 insulating film, 58 backside electrode.
Number | Date | Country | Kind |
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2008-257280 | Oct 2008 | JP | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/JP2009/064002 | 8/7/2009 | WO | 00 | 3/30/2011 |