The present invention relates to a composite GaN substrate suitably used for a group III nitride semiconductor device, a method for manufacturing the composite GaN substrate, a group III nitride semiconductor device including the composite GaN substrate, and a method for manufacturing the group III nitride semiconductor device.
In recent years, group III nitride semiconductor devices are widely applied not only to optical devices but also to electronic devices such as high electron mobility transistors (hereinafter, abbreviated as “HEMT”).
For example, Yamada et al, “Effect of Epitaxial Layer Design on Drain Leakage Current for Millimeter-Wave GaN-HEMT”, IEICE Technical Report, ED2009-48, The Institute of Electronics, Information and Communication Engineers, June 2009, pp 63-67 (Non-Patent Literature 1) discloses a HEMT in which an i-GaN layer, an n-AlGaN layer, and an n-GaN layer are sequentially formed on a semi-insulative SiC substrate. Meanwhile, K. K. Chu et al, “9.4-W/mm Power Density AlGaN—GaN HEMTs on Free-Standing GaN Substrates”, IEEE ELECTRON DEVICE LETTERS, Institute of Electrical and Electronic Engineers, VOL. 25, NO. 9, SEPTEMBER 2004, pp 596-598 (Non-Patent Literature 2) discloses a HEMT in which a GaN layer and an AlGaN layer are sequentially formed on a semi-insulative, freestanding GaN substrate.
NPL 1: Yamada et al., “Effect of Epitaxial Layer Design on Drain Leakage Current for Millimeter-Wave GaN-HEMT”, IEICE Technical Report, ED2009-48, The Institute of Electronics, Information and Communication Engineers, June 2009, pp 63-67
NPL 2: K. K. Chu et al, “9.4-W/mm Power Density AlGaN—GaN HEMTs on Free-Standing GaN Substrates”, IEEE ELECTRON DEVICE LETTERS, Institute of Electrical and Electronic Engineers, VOL. 25, NO. 9, SEPTEMBER 2004, pp 596-598
However, the HEMT disclosed in Yamada et al, “Effect of Epitaxial Layer Design on Drain Leakage Current for Millimeter-Wave GaN-HEMT”, IEICE Technical Report, ED2009-48, The Institute of Electronics, Information and Communication Engineers, June 2009, pp 63-67 (Non-Patent Literature 1), i.e., the HEMT including the GaN layer/AlGaN layer formed on the semi-insulative SiC substrate has a multiplicity of defects resulting from mismatching of crystal lattices between the SiC substrate and the GaN layer/AlGaN layer. Accordingly, deficiencies such as current drift are noticeable, disadvantageously.
On the other hand, the HEMT disclosed in K. K. Chu et al, “9.4-W/mm Power Density AlGaN—GaN HEMTs on Free-Standing GaN Substrates”, IEEE ELECTRON DEVICE LETTERS, Institute of Electrical and Electronic Engineers, VOL. 25, NO. 9, SEPTEMBER 2004, pp 596-598 (Non-Patent Literature 2), i.e., the HEMT including the GaN layer/AlGaN layer formed on the semi-insulative GaN substrate has little defects because matching of crystal lattices is excellent between the GaN substrate and the GaN layer/AlGaN layer. Accordingly, deficiencies such as current drift are little. However, because the semi-insulative GaN substrate is very expensive, the HEMT will be expensive, disadvantageously.
In view of this, the present invention has its object to provide a composite GaN substrate having a high characteristic with reasonable cost, a method for manufacturing such a composite GaN substrate, and a group III nitride semiconductor device, and a method for manufacturing the group III nitride semiconductor device.
According to a certain aspect, the present invention provides a composite GaN substrate including: a conductive GaN substrate having a specific resistance of less than 1 Ωcm; and a semi-insulative GaN layer disposed on the conductive GaN substrate, having a specific resistance of 1×104 Ωcm or more, and having a thickness of 5 μm or more.
In the composite GaN substrate according to the present invention, the semi-insulative GaN layer can contain at least one kind of atoms selected from a group consisting of C, Fe, Cr, and V, as an impurity. Further, the semi-insulative GaN layer can contain C atoms as an impurity at a concentration of not less than 1×1017 cm3 and not more than 5×1019 cm−3.
According to another aspect, the present invention provides a group III nitride semiconductor device including: the above-described composite GaN substrate; and at least one group III nitride semiconductor layer disposed on the semi-insulative GaN layer of the composite GaN substrate.
In the group III nitride semiconductor device according to the present invention, the group III nitride semiconductor layer can include an electron transit layer and an electron supply layer.
According to still another aspect, the present invention provides a method for manufacturing a composite GaN substrate, including the steps of: preparing a conductive GaN substrate having a specific resistance of less than 1 Ωcm; and growing a semi-insulative GaN layer on the conductive GaN substrate using an HVPE (hydride vapor phase epitaxy) method, the semi-insulative GaN layer having a specific resistance of 1×104 Ωcm or more and having a thickness of 5 μm or more.
In the method for manufacturing the composite GaN substrate according to the present invention, the semi-insulative GaN layer can contain at least one kind of atoms selected from a group consisting of C, Fe, Cr, and V, as an impurity. Further, the semi-insulative GaN layer can contain C atoms as an impurity at a concentration of not less than 1×1017 cm3 and not more than 5×1019 cm3.
According to yet another aspect, the present invention provides a method for manufacturing a group III nitride semiconductor device, including the steps of: preparing the composite GaN substrate obtained through the above-described method for manufacturing the composite GaN substrate; and growing at least one group III nitride semiconductor layer on the semi-insulative GaN layer of the composite GaN substrate, using at least one of an MOVPE (metalorganic vapor phase epitaxy) method and an MBE (molecular beam epitaxy) method.
In the method for manufacturing the group III nitride semiconductor device according to the present invention, the group III nitride semiconductor layer can include an electron transit layer and an electron supply layer.
According to the present invention, there can be provided a composite GaN substrate having a high characteristic with reasonable cost, a method for manufacturing such a composite GaN substrate, a group III nitride semiconductor device, and a method for manufacturing the group III nitride semiconductor device.
Referring to
(Conductive GaN Substrate)
Conductive GaN substrate 10 in composite GaN substrate 1 of the present embodiment is a single crystal having a specific resistance of less than 1 Ωcm. Here, the specific resistance of conductive GaN substrate 10 can be measured using a van der Pauw method or the like.
There is no particular limitation as to a method for obtaining such a conductive GaN substrate. In the case where a single-crystal substrate is employed therefor to obtain a substrate having good crystal quality, the following methods are suitable: vapor phase methods such as an HVPE (hydride vapor phase epitaxy) method, an MOVPE (metalorganic vapor phase epitaxy) method, and an MBE (molecular beam epitaxy) method; and liquid phase methods such as a flux method, and a high nitrogen pressure solution method.
Further, a donor impurity is generally added to conductive GaN substrate 10. For example, in order to reduce the specific resistance of conductive GaN substrate 10, conductive GaN substrate 10 can contain atoms such as O, Si, or Ge as the donor impurity.
(Semi-Insulative GaN Layer)
In order to suitably form an electronic device such as a HEMT as a semiconductor device, semi-insulative GaN layer 20 in composite GaN substrate 1 of the present embodiment needs to have a specific resistance of 1×104 Ωcm or more and have a thickness of 5 μm or more.
There is no particular limitation as to semi-insulative GaN layer 20 as long as semi-insulative GaN layer 20 has a specific resistance of 1×104 Ωcm or more and has a thickness of 5 μm or more. However, in order to efficiently attain semi-insulation with the specific resistance of 1×104 Ωm or more, semi-insulative GaN layer 20 preferably contains atoms of an impurity such as C, Fe, Cr, V, Mg, or Zn. In order to stably attain the above-described semi-insulation, semi-insulative GaN layer 20 preferably contains at least one kind of atoms selected from a group consisting of C, Fe, Cr, and V, as the impurity. Further, in order to suppress the impurity in semi-insulative GaN layer 20 from being diffused into conductive GaN substrate 10 and a group III nitride semiconductor layer to be formed on semi-insulative GaN layer 20, semi-insulative GaN layer 20 more preferably contains C atoms as the impurity at a concentration of not less than 1×1017 cm−3 and not more than 5×1019 cm−3. When the concentration of the C atoms is less than 1×1017 cm−3, it is difficult to obtain semi-insulative GaN layer 20 having a high resistance, i.e., having a specific resistance of 1×104 Ωcm or more. On the other hand, when the concentration of the C atoms is more than 5×1019 cm−3, the crystal quality of semi-insulative GaN layer 20 is decreased.
Further, there is no particular limitation as to a method for forming semi-insulative GaN layer 20 described above. However, in order to obtain a substrate having good crystal quality, the following methods are suitable: vapor phase methods such as the HVPE method, the MOVPE method, the MBE method, and a sublimation method; and liquid phase methods such as the flux method, and the high nitrogen pressure solution method. Of these methods, the HVPE method, which allows for high crystal quality and high crystal growth rate, is particularly suitable because it is advantageous to form a thick layer.
Referring to
(Composite GaN Substrate)
Composite GaN substrate 1 in group III nitride semiconductor device 2 of the present embodiment is the same as composite GaN substrate 1 of the first embodiment, and is not therefore described repeatedly here.
(Group III Nitride Semiconductor Layer)
There is no particular limitation as to group III nitride semiconductor layer 30 in group III nitride semiconductor device 2 of the present embodiment. However, in order to form an electronic device such as a HEMT, group III nitride semiconductor layer 30 preferably includes an electron transit layer 32 and an electron supply layer 34. Further, there is no particular limitation as to electron transit layer 32 serving as group III nitride semiconductor layer 30. However, in order to improve electron mobility, electron transit layer 32 is preferably a GaN layer. Also, there is no particular limitation as to electron supply layer 34 serving as group III nitride semiconductor layer 30. However, in order to attain a high concentration of 2DEG (two dimensional electron gas), electron supply layer 34 is preferably an AlxGa1-xN layer (0<x<1), an InyAl1-yN layer (0<y<0.3), or the like.
Further, there is no particular limitation as to a method for forming group III nitride semiconductor layer 30. However, in order to obtain a semiconductor layer having good crystal quality, the following methods are suitable: vapor phase methods such as the HVPE method, the MOVPE method, the MBE method, and the sublimation method; and liquid phase methods such as the flux method, and the high nitrogen pressure solution method. Of these methods, at least one of the MOVPE method and the MBE method is particularly suitable because these methods allow for a semiconductor layer having high crystal quality and are advantageous in adjusting the thickness of the semiconductor layer.
(Electrodes)
Referring to
Here, a material of each of source electrode 42 and drain electrode 44 is not particularly limited. An electrode formed of Ti layer/Al layer/Ti layer/Au layer is suitably used therefor. Also, a material of gate electrode 46 is not particularly limited. An electrode formed of Ni layer/Au layer is suitably used therefor.
Referring to
(Step of Preparing Conductive GaN Substrate)
Referring to
Further, conductive GaN substrate 10 can contain atoms such as, O, Si, or Ge as an impurity in order to reduce the specific resistance thereof.
(Step of Growing Semi-Insulative GaN Layer)
Referring to
Here, there is no particular limitation as to a manner of achieving the specific resistance of 1×104 Ωcm or more in semi-insulative GaN layer 20 during the growth thereof. However, semi-insulative GaN layer 20 is preferably adapted to contain atoms such as C, Fe, Cr, V, Mg, or Zn as an impurity. In order to stably attain the above-described semi-insulation, semi-insulative GaN layer 20 preferably contains at least one kind of atoms selected from a group consisting of C, Fe, Cr, and V, as the impurity.
Further, in order to suppress the impurity in semi-insulative GaN layer 20 from being diffused into group III nitride semiconductor layer 30 to be formed on semi-insulative GaN layer 20, semi-insulative GaN layer 20 more preferably contains C atoms as the impurity at a concentration of not less than 1×1017 cm−3 and not more than 5×1019 cm−3. When the concentration of the C atoms is less than 1×1017 cm−3, it becomes difficult to obtain semi-insulative GaN layer 20 having a specific resistance of 1×104 Ωcm or more. On the other hand, when the concentration of the C atoms is more than 5×1019 cm−3, the crystal quality of semi-insulative GaN layer 20 is decreased.
Referring to
(Step of Preparing Composite GaN Substrate)
Referring to
(Step of Growing Group III Nitride Semiconductor Layer)
Referring to
Here, for the method for growing group III nitride semiconductor layer 30, at least one of the MOVPE method and the MBE method is employed because these methods allow for a semiconductor layer having high crystal quality and are advantageous in adjusting the thickness of the semiconductor layer.
Further, there is no particular limitation as to group III nitride semiconductor layer 30 to be grown. However, in order to form an electronic device such as a HEMT, group III nitride semiconductor layer 30 preferably includes electron transit layer 32 and electron supply layer 34. Further, there is no particular limitation as to electron transit layer 32. However, in order to improve electron mobility, electron transit layer 32 is preferably a GaN layer. Further, there is no particular limitation as to electron supply layer 34. However, in order to attain a high concentration of 2DEG (two dimensional electron gas), electron supply layer 34 is preferably an AlxGa1-xN layer (0<x<1), an InyAl1-yN layer (0<y<0.3), or the like.
(Step of Forming Electrodes)
Referring to
Here, there is no particular limitation as to a method for forming each of source electrode 42 and drain electrode 44. For example, source electrode 42 and drain electrode 44 are formed on surfaces of parts of electron supply layer 34 by means of a lift-off method or the like employing photolithography and deposition. Then, heat treatment is performed to diffuse atoms in source electrode 42 and drain electrode 44 into the parts of electron supply layer 34. In this way, they are brought into ohmic contact with parts of electron supply layer 34 and electron transit layer 32.
Further, there is no particular limitation as to a method for forming gate electrode 46. For example, gate electrode 46 is formed on a surface of a part of electron supply layer 34 by means of the lift-off method or the like employing photolithography and deposition, so as to make Schottky contact with the part of electron supply layer 34.
1. Preparation of Conductive GaN substrate
Referring to
2. Growth of Semi-Insulative GaN Layer
Referring to
The C atom concentration of each of the six types of GaN layers thus obtained was measured using a SIMS (secondary ion mass spectrometry) method. The specific resistance thereof was measured using a two-probe method. The crystal quality thereof was evaluated through X-ray diffraction. The surface state thereof was observed using a Nomarski interference microscope. Criteria for evaluation of the crystal quality were as follows: the crystal quality was regarded as “very good” when the half width of the peak of the diffraction intensity resulting from the (0002) plane of the GaN layer was 50 arcsec or less; the crystal quality was regarded as “good” when the half width was more than 50 arcsec and 200 arcsec or less; and the crystal quality was regarded as “bad” when the half width was more than 200 arcsec. Criteria for evaluation of the surface state were as follows: the surface state was regarded as “very good” when no macrostep and crack were generated in the surface; the surface state was regarded as “good” when macrostep was generated in the surface but no crack was generated therein; the surface state was regarded as “bad” when macrostep and crack were generated in the surface.
The GaN layer of Example A-1 had a C atom concentration of 5×1016 cm−3, had a specific resistance of 5×10−2 Ωcm, and had very good crystal quality and surface state. The GaN layer of Example A-2 had a C atom concentration of 1×1017 cm−3, had a specific resistance of 1×104 Ωcm, and had very good crystal quality and surface state. The GaN layer of Example A-3 had a C atom concentration of 1×1018 cm−3, had a specific resistance of more than 1×107 Ωcm, and had very good crystal quality and surface state. The GaN layer of Example A-4 had a C atom concentration of 1×1019 cm−3, had a specific resistance of more than 1×107 Ωcm, and had very good crystal quality and surface state. The GaN layer of Example A-5 had a C atom concentration of 5×1019 cm−3, had a specific resistance of more than 1×107 Ωcm, and had good crystal quality and surface state. The GaN layer of Example A-6 had a C atom concentration of 7×1019 cm−3, had a specific resistance of more than 1×107 Ωcm, and had bad crystal quality and surface state. These results are collectively shown in Table 1.
Referring to Table 1, as the CH4 gas partial pressure was increased during the growth of each GaN layer, the C atom concentration and specific resistance of the GaN layer were increased. When the CH4 gas partial pressure was 1.0×10−4 atm or more, there were obtained the semi-insulative GaN layers each having a C atom concentration of 1×1017 cm−3 or more and having a specific resistance of 1×104 Ωcm or more. When the CH4 gas partial pressure became too high, the crystal quality and the surface state of the GaN layer were decreased. For example, when the CH4 gas partial pressure was 5.0×10−2 atm, the half width of the peak of the diffraction intensity in the X-ray diffraction became 100 arcsec, with the result that a multiplicity of macrosteps were generated in the surface. Further, when the CH4 gas partial pressure was 7.0×10−2 atm, the half width of the peak of the diffraction intensity in the X-ray diffraction became 1000 arcsec, with the result that a multiplicity of macrosteps and a multiplicity of cracks were generated in the surface.
1. Preparation of Composite GaN Substrate
Referring to
In addition, a conductive GaN substrate 10 similar to that of Example A was prepared. A different type of composite GaN substrate 1 (Example B-4) was obtained by growing a semi-insulative GaN layer 20 on conductive GaN substrate 10 under the same conditions as those in Example A except that CpFe (ferrocene) was used instead of the CH4 gas. Semi-insulative GaN layer 20 was grown to contain Fe at a concentration of 3×1019 cm−3, have a specific resistance of more than 1×107 Ωcm, and have a thickness of 10 μm.
2. Growth of Group III Nitride Semiconductor Layer
Referring to
Group III nitride semiconductor layer 30 was grown in the following procedure. First, the four types of semi-insulative GaN layer 20 of composite GaN substrate 1 in Example B-1 to Example B-4 were subjected to heat treatment in a reactor under an atmosphere of H2 gas, N2 gas, and NH3 gas at a substrate temperature of 1100° C. for 20 min. Next, the substrate temperature was set at 1130° C. and NH3 gas and TMG (trimethylgallium) were supplied to the reactor, so as to grow a GaN layer serving as electron transit layer 32 and having a thickness of 2.0 μm. Next, TMA (trimethylaluminum), TMG, and NH3 gas were supplied to the reactor so as to grow an Al0.2Gaa8N layer serving as electron supply layer 34 and having a thickness of 30 nm.
Further, referring to
The concentration (sheet carrier concentration) of 2DEG (two dimensional electron gas) formed in the vicinity of an interface between each of electron transit layers 32, 132 and each of electron supply layers 34, 134 thus obtained was measured through the following evaluation of C-V characteristics. Specifically, in such evaluation of C-V characteristics, sheet carrier concentration Ns of the 2DEG was calculated in the following manner. That is, on the surface of each of electron supply layers 34, 134 formed on electron transit layers 32, 132 formed on the substrates, a double-Schottky pattern having a diameter of 200 μm was formed from a Ni/Au electrode by means of the photolithography method. From C-V measurement thereof, the carrier concentration profile of the 2DEG layer was calculated and then integrated. The 2DEGs formed around the interfaces between electron transit layers 32, 132 and electron supply layers 34, 134 in Example B-1 to Example B-5 were respectively at sheet carrier concentrations Ns of 1.1×1013 cm−2 (Example B-1), 1.1×1013 cm−2 (Example B-2), 1.1×1013 cm−2 (Example B-3), 0.9×1013 cm−2 (Example B-4), and 1.0×1013 cm−2 (Example B-5). The results are collectively shown in Table 2.
3. Formation of Electrodes
Referring to
Referring to Table 2, sheet carrier concentration Ns of the 2DEG in the electron transit layer and the electron supply layer formed on each of the semi-insulative GaN layers having C atoms added therein in Example B-1 to Example B-3 was 1.1×1013 cm−2, which was a high value. On the other hand, in Example B-4, sheet carrier concentration Ns of the 2DEG in the electron transit layer and the electron supply layer formed on the semi-insulative GaN layer having Fe atoms added therein was 0.9×1013 cm−2, which was somewhat lower than that in each of Example B-1 to Example B-3. This is presumably because the Fe atoms added in the semi-insulative GaN layer are diffused into these layers during growth of the electron transit layer and the electron supply layer. Meanwhile, in Example B-5, sheet carrier concentration Ns of the 2DEG in the electron transit layer and the electron supply layer formed on the AlN buffer layer formed on the semi-insulative SiC substrate was 1.0×1013 cm−2, which was somewhat lower than that in each of Example B-1 to Example B-3. This is presumably because dislocations formed in an interface between the semi-insulative SiC substrate and the AlN buffer layer and an interface between the AlN buffer layer and the electron transit layer result in carrier compensation.
Further, the HEMT (Example B-5) employing the typical semi-insulative SiC substrate had a cutoff frequency fT of 10 GHz. The HEMT (Example B-1) including the semi-insulative GaN layer having a thickness of 10 μm had a cutoff frequency fT of 8 GHz, i.e., had a high-frequency characteristic comparable to that of the HEMT employing the semi-insulative SiC substrate. The HEMT (Example B-2) including the semi-insulative GaN layer having a thickness of 5 μm had a cutoff frequency fT of 6 GHz, i.e., had a practically usable high-frequency characteristic. The HEMT (Example B-3) including the semi-insulative GaN layer having a thickness of 2 μm had a cutoff frequency fT of 2 GHz, i.e., had a high-frequency characteristic abruptly decreased therefrom. As such, it was found that a practically usable HEMT can be obtained by forming a semi-insulative GaN layer having a thickness of 5 μm or more on a conductive GaN substrate, and that a HEMT having a high-frequency characteristic comparable to or more excellent than the high-frequency characteristic of a HEMT employing a typical semi-insulating substrate can be obtained by forming a semi-insulative GaN layer having a thickness of 10 μm or more on a conductive GaN substrate.
Particularly, the semiconductor device (for example, the HEMT) of the invention of the present application is obtained by growing the group III nitride semiconductor layer on the composite GaN substrate including the conductive GaN substrate and the semi-insulative GaN layer, so that crystal lattice matching is very high between the composite GaN substrate and the group III nitride semiconductor layer. Thus, by using the composite GaN substrate having a low dislocation density, the dislocation density of the group III nitride semiconductor layer to be grown thereon becomes low. Hence, bad characteristics such as current drift, which cannot be improved by the typical semiconductor device (for example, the HEMT) employing the typical semi-insulative SiC substrate, can be improved.
The embodiments and examples disclosed herein are illustrative and non-restrictive in any respect. The scope of the present invention is defined by the terms of the claims, rather than the embodiments described above, and is intended to include any modifications within the scope and meaning equivalent to the terms of the claims.
1: composite GaN substrate; 2, 102: group III nitride semiconductor device; 10: conductive GaN substrate; 20: semi-insulative GaN layer; 30, 130: group III nitride semiconductor layer; 32, 132: electron transit layer; 34, 134: electron supply layer; 42, 142: source electrode; 44, 144: drain electrode; 46, 146: gate electrode; 110: semi-insulative SiC substrate; 120: AlN buffer layer.
Number | Date | Country | Kind |
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2011-062795 | Mar 2011 | JP | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/JP2011/076887 | 11/22/2011 | WO | 00 | 3/15/2013 |