SEMICONDUCTOR CRYSTAL SUBSTRATE, INFRARED DETECTOR, METHOD FOR PRODUCING SEMICONDUCTOR CRYSTAL SUBSTRATE, AND METHOD FOR PRODUCING INFRARED DETECTOR
20170358613 · 2017-12-14
Assignee
Inventors
Cpc classification
H01L31/1844
ELECTRICITY
H01L31/03046
ELECTRICITY
H01L21/02631
ELECTRICITY
International classification
H01L31/18
ELECTRICITY
H01L31/0304
ELECTRICITY
Abstract
A semiconductor crystal substrate includes a crystal substrate that is formed of a material including one of GaSb and InAs, a first buffer layer that is formed on the crystal substrate and formed of a material including GaSb, and a second buffer layer that is formed on the first buffer layer and formed of a material including GaSb. The first buffer layer has a p-type conductivity, and the second buffer layer has an n-type conductivity.
Claims
1. A semiconductor crystal substrate, comprising: a crystal substrate that is formed of a material including one of GaSb and InAs; a first buffer layer that is formed on the crystal substrate and formed of a material including GaSb, the first buffer layer having a p-type conductivity; and a second buffer layer that is formed on the first buffer layer and formed of a material including GaSb, the second buffer layer having an n-type conductivity.
2. The semiconductor crystal substrate as claimed in claim 1, wherein a concentration of a dopant in the first buffer layer is less than or equal to 1.0×10.sup.17 cm.sup.−3; a carrier concentration in the first buffer layer is greater than or equal to 1×10.sup.18 cm.sup.−3 and less than or equal to 1×10.sup.20 cm.sup.−3; a concentration of a dopant in the second buffer layer is less than or equal to 1.0×10.sup.17 cm.sup.−3; and a carrier concentration in the second buffer layer is greater than or equal to 1×10.sup.18 cm.sup.−3 and less than or equal to 1×10.sup.20 cm.sup.−3.
3. The semiconductor crystal substrate as claimed in claim 1, wherein the first buffer layer is formed of the material including GaSb and one or both of In and As; and the second buffer layer is formed of the material including GaSb and one or both of In and As.
4. An infrared detector, comprising: a crystal substrate that is formed of a material including one of GaSb and InAs; a first buffer layer that is formed on the crystal substrate and formed of a material including GaSb, the first buffer layer having a p-type conductivity; a second buffer layer that is formed on the first buffer layer and formed of a material including GaSb, the second buffer layer having an n-type conductivity; a first contact layer that is formed on the second buffer layer and has a first conductivity type; an infrared absorption layer that is formed on the first contact layer and has a superlattice structure; and a second contact layer that is formed on the infrared absorption layer and has a second conductivity type.
5. The infrared detector as claimed in claim 4, wherein a concentration of a dopant in the first buffer layer is less than or equal to 1.0×10.sup.17 cm.sup.−3; a carrier concentration in the first buffer layer is greater than or equal to 1×10.sup.18 cm.sup.−3 and less than or equal to 1×10.sup.20 cm.sup.−3; a concentration of a dopant in the second buffer layer is less than or equal to 1.0×10.sup.17 cm.sup.−3; and a carrier concentration in the second buffer layer is greater than or equal to 1×10.sup.18 cm.sup.−3 and less than or equal to 1×10.sup.20 cm.sup.−3.
6. The infrared detector as claimed in claim 4, wherein the first buffer layer is formed of the material including GaSb and one or both of In and As; and the second buffer layer is formed of the material including GaSb and one or both of In and As.
7. The infrared detector as claimed in claim 4, wherein the first conductivity type of the first contact layer is a p-type, and the first contact layer is formed of a material including GaSb; the infrared absorption layer has the superlattice structure that is formed by alternately stacking a GaSb layer and an InAs layer; and the second conductivity type of the second contact layer is an n-type, and the second contact layer is formed of a material including InAs.
8. The infrared detector as claimed in claim 4, wherein pixel separating grooves are formed in the second contact layer and the infrared absorption layer to separate pixels of the infrared detector.
9. A method of producing a semiconductor crystal substrate, the method comprising: forming a first buffer layer on a crystal substrate by molecular beam epitaxy with a material including GaSb, the crystal substrate being formed of a material including one of GaSb and InAs; and forming a second buffer layer on the first buffer layer by the molecular beam epitaxy with a material including GaSb, wherein the first buffer layer is formed at a substrate temperature greater than or equal to 470° C. and less than or equal to 550° C.; and the second buffer layer is formed at a substrate temperature greater than or equal to 420° C. and less than or equal to 460° C.
10. The method as claimed in claim 9, wherein the first buffer layer is formed at a substrate temperature greater than or equal to 500° C. and less than or equal to 550° C.
11. The method as claimed in claim 9, wherein the molecular beam epitaxy is solid source molecular beam epitaxy.
12. The method as claimed in claim 9, wherein the first buffer layer is formed of the material including GaSb and one or both of In and As; and the second buffer layer is formed of the material including GaSb and one or both of In and As.
13. A method of producing an infrared detector, the method comprising: forming a first contact layer having a first conductivity type on the second buffer layer of the semiconductor crystal substrate produced by the method of claim 9; forming an infrared absorption layer having a superlattice structure on the first contact layer; and forming a second contact layer having a second conductivity type on the infrared absorption layer.
14. The method as claimed in claim 13, wherein the first conductivity type of the first contact layer is a p-type, and the first contact layer is formed of a material including GaSb; the infrared absorption layer has the superlattice structure that is formed by alternately stacking a GaSb layer and an InAs layer; and the second conductivity type of the second contact layer is an n-type, and the second contact layer is formed of a material including InAs.
Description
BRIEF DESCRIPTION OF DRAWINGS
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DESCRIPTION OF EMBODIMENTS
[0031] Although “M. Lee et al., Journal of Applied Physics 59, 2895 (1986)” proposes improving the quality of a GaSb buffer layer as described above, it is not possible to form a high-quality T2SL crystal that fully satisfies the desired characteristics of an infrared absorption layer by just forming a GaSb buffer layer under various conditions. Accordingly, there is a demand for a semiconductor crystal substrate including a GaSb buffer layer with a highly-flat surface.
[0032] Embodiments of the present invention are described below with reference to the accompanying drawings. The same reference numbers are assigned to the same components throughout the drawings, and repeated descriptions of those components are omitted.
First Embodiment
[0033] The inventors studied the relationship between film-forming conditions and flatness of a GaSb film. Specifically, as illustrated by
[0034] An oxide film formed on a surface of the GaSb substrate 11 was removed by heating the GaSb substrate 11 at a temperature of about 500° C. in vacuum.
[0035] Next, the GaSb layer 12a with a thickness of 500 nm was formed by MBE at a substrate temperature of 520° C. on the GaSb substrate 11 from which the oxide film was removed.
[0036] Also, the GaSb layer 12b with a thickness of 500 nm was formed by MBE at a substrate temperature of 440° C. on the GaSb substrate 11 from which the oxide film was removed.
[0037] Here, as can be seen in
[0038] On the other hand, as can be seen in
[0039] Next, the conductivity of the GaSb layer 12a and the GaSb layer 12b formed at different substrate temperatures was examined. As a result of the examination, it was found out that the GaSb layer 12a formed by MBE at the substrate temperature of 520° C. had p-type conductivity, and the GaSb layer 12b formed by MBE at the substrate temperature of 440° C. had n-type conductivity. Also, the carrier concentrations in the GaSb layer 12a formed at the substrate temperature of 520° C. and the GaSb layer 12b formed at the substrate temperature of 440° C. were measured by using a capacitance-voltage (CV) technique. The carrier concentration in the GaSb layer 12a was about 1×10.sup.18 cm.sup.−3, and the carrier concentration in the GaSb layer 12b was about 4×10.sup.18 cm.sup.−3. Further, the GaSb layer 12a and the GaSb layer 12b were analyzed by secondary ion mass spectrometry (SIMS), and it was found out that the concentration of an impurity element (dopant) in each of the GaSb layer 12a and the GaSb layer 12b was less than or equal to 1×10.sup.17 cm.sup.−3.
[0040] The above results indicate that Sb is easily removed from a formed GaSb layer when the substrate temperature is high, and the amount of Ga is slightly greater than the amount of Sb in the GaSb layer 12a formed by MBE at the substrate temperature of 520° C. Accordingly, it is assumed that a part of Ga enters the site of Sb in the GaSb crystal and as a result, the GaSb layer 12a exhibits p-type conductivity. The above results also indicate that the removal of Sb from a formed GaSb layer is suppressed when the substrate temperature is low, and the amount of Sb is slightly greater than the amount of Ga in the GaSb layer 12b formed by MBE at the substrate temperature of 440° C. Accordingly, it is assumed that a part of Sb enters the site of Ga in the GaSb crystal and as a result, the GaSb layer 12b exhibits n-type conductivity.
[0041] Here, when the substrate temperature during the formation of a GaSb layer is high, the movement of Ga atoms due to surface migration becomes active. On the other hand, when the substrate temperature is low, the movement of Ga atoms due to surface migration becomes less active. Accordingly, it is assumed that the distance of movement of Ga atoms due to surface migration becomes long in the GaSb layer 12a formed at the substrate temperature of 520° C. and as a result, the surface of the GaSb layer 12a becomes flatter than the surface of the GaSb layer 12b formed at the substrate temperature of 440° C. Also, it is known that when the composition ratio of Ga is high, Ga tends to form clusters. Accordingly, it can be considered that the pits in the surface of the GaSb layer 12a formed at the substrate temperature of 520° C. are formed at the boundaries between the clusters.
[0042] Thus, the GaSb layer 12a formed at the substrate temperature of 520° C. becomes rich in Ga, this Ga enters the site of Sb and functions as an acceptor, and as a result, the GaSb layer 12a exhibits p-type conductivity. The GaSb layer 12a formed at a high substrate temperature has low surface roughness (RMS) and high flatness. However, pits tend to be formed in the GaSb layer 12a due to a high composition ratio of Ga.
[0043] On the other hand, the GaSb layer 12b formed at the substrate temperature of 440° C. becomes rich in Sb, this Sb enters the site of Ga and functions as a donor, and as a result, the GaSb layer 12b exhibits n-type conductivity. Compared with the GaSb layer 12a formed at the substrate temperature of 520° C., the GaSb layer 12b formed at a lower substrate temperature has slightly higher surface roughness (RMS). However, no pit is formed in the GaSb layer 12b because the composition ratio of Ga is low.
<Semiconductor Crystal Substrate>
[0044] A semiconductor crystal substrate according to a first embodiment is obtained based on the above findings. As illustrated by
[0045]
[0046] Possible reasons why a film having a flat surface with not pit can be formed are explained below. First, because the first GaSb layer 112 is formed at a high substrate temperature of 520° C., the first GaSb layer 112 becomes rich in Ga and although pits are formed, the first GaSb layer 112 becomes mostly flat. Second, because the second GaSb layer 113 is formed on the first GaSb layer 112 at a low substrate temperature of 440° C., the second GaSb layer 113 becomes rich in Sb and no pit is formed in the surface of the second GaSb layer 113. Also, it is assumed that atoms moved due to surface migration fill the pits. These are assumed to be the reasons why the surface roughness (RMS) of the second GaSb layer 113 becomes 0.10 nm that is less than the surface roughness (RMS) 0.13 nm of the GaSb layer 12a formed at the surface temperature of 520° C. and the surface roughness (RMS) 0.16 nm of the GaSb layer 12b formed at the surface temperature of 440° C. The concentration of an impurity element (dopant) in each of the GaSb layer 112 and the GaSb layer 113 is less than or equal to 1×10.sup.17 cm.sup.−3 and is substantially the same as that in the GaSb layer 12a and the GaSb layer 12b.
[0047]
[0048]
[0049] In the present embodiment, the carrier concentration in each of the first GaSb layer 112 having p-type conductivity and the second GaSb layer 113 having n-type conductivity is preferably greater than or equal to 1×10.sup.18 cm.sup.−3 and less than or equal to 1×10.sup.20 cm.sup.−3. The first GaSb layer 112 with such a carrier concentration can be formed by solid source molecular beam epitaxy (SSMBE) at a substrate temperature greater than or equal to 500° C. and less than or equal to 550° C. Also, the second GaSb layer 113 with such a carrier concentration can be formed by solid source molecular beam epitaxy (SSMBE) at a substrate temperature greater than or equal to 420° C. and less than or equal to 460° C.
[0050] As described above, the semiconductor crystal substrate of the present embodiment includes the GaSb substrate 111 that is a crystal substrate, the first GaSb layer 112 formed on the GaSb substrate 111, and the second GaSb layer 113 formed on the first GaSb layer 112. The first GaSb layer 112 is rich in Ga and has p-type conductivity, and the second GaSb layer 113 is rich in Sb and has n-type conductivity. In the present application, the first GaSb layer 112 may be referred to as a first buffer layer, and the second GaSb layer 113 may be referred to as a second buffer layer.
[0051] Also in the present embodiment, each of the first buffer layer and the second buffer layer may be formed of Ga.sub.1-xIn.sub.xAs.sub.1-ySb.sub.y (0≦x≦0.1, 0≦y<1). More specifically, each of the first buffer layer and the second buffer layer may be formed of GaInSb, GaAsSb, or GaInAsSb that is a material including In and/or As in addition to GaSb.
<Method for Producing Semiconductor Crystal Substrate>
[0052] Next, an exemplary method for producing a semiconductor crystal substrate according to the present embodiment is described with reference to
[0053] Next, as illustrated by
[0054] Next, as illustrated by
[0055] Through the above process, the semiconductor crystal substrate of the present embodiment is produced. Although an n-type GaSb substrate is used as the GaSb substrate 111 in the present embodiment, a p-type GaSb substrate may also be used as the GaSb substrate 111. Also, the plane direction of the GaSb substrate 111 is not limited to (001), and an off substrate may also be used as the GaSb substrate 111. Further, an InAs substrate may be used in place of the GaSb substrate 111.
Second Embodiment
[0056] Next, a second embodiment is described. In the second embodiment, an infrared detector produced by using the semiconductor crystal substrate of the first embodiment is described.
[0057] As illustrated by
[0058] Pixel separating grooves 120 are formed in the n-type contact layer 116 and the infrared absorption layer 115 to separate pixels of the infrared detector. A passivation film 131 composed of SiN is formed on the side surfaces and the bottom surfaces of the pixel separating grooves 120. In the infrared detector of the present embodiment, multiple pixels separated by the pixel separating grooves 120 are arranged two-dimensionally. An electrode 141 is formed on the n-type contact layer 116 of each of the pixels separated by the pixel separating grooves 120, and an electrode 142 is formed on the p-type contact layer 114. The infrared absorption layer 115 and the n-type contact layer 116 near the electrode 142 form a wiring support 143. Also, a wiring layer 144 is formed to extend from the electrode 142, via the side surface of the wiring support 143, to the upper surface of the wiring support 143. Accordingly, the infrared absorption layer 115 and the n-type contact layer 116 forming the wiring support 143 are not used for infrared detection. Each of the electrodes 141 and 142 is formed of a metal multilayer film of Ti, Pt, and Au. In the present embodiment, a structure or a device with the above configuration may be referred to as an infrared detector or an infrared detecting device 150. The infrared detector of the present embodiment can detect infrared radiation that enters from the back side of the GaSb substrate 111.
[0059] As illustrated by
<Method for Producing Infrared Detector>
[0060] Next, an exemplary method for producing an infrared detector according to the second embodiment is described with reference to
[0061] First, as illustrated by
[0062] Specifically, the first GaSb layer 112 and the second GaSb layer 113 are sequentially formed on the GaSb substrate 111, and the p-type contact layer 114 is formed on the second GaSb layer 113. The p-type contact layer 114 is a p-type GaSb layer that is formed by emitting Ga, Sb, and Be beams. In this step, the temperature of the Be cell is adjusted so that the concentration of Be that is an impurity element used as a dopant of the p-type contact layer 114 becomes 5.0×10.sup.18 cm.sup.−3. Also in this step, the beam flux of Ga is 5.0×10.sup.−8 Torr, the beam flux of Sb is 5.0×10.sup.−7 Torr, and the V/III ratio is 10. Under these conditions, the growth rate of GaSb is 0.30 μm/h. Film forming is performed for about 100 minutes until the thickness of the p-type contact layer 114 reaches 500 nm, and then the Be and Ga beams are stopped.
[0063] Next, the infrared absorption layer 115 with an InAs/GaSb superlattice structure is formed on the p-type contact layer 114. Specifically, the Sb beam is stopped, and In and As beams are emitted. In this step, the beam flux of In is 5.0×10.sup.−8 Torr, the beam flux of As is 5.0×10.sup.−7 Torr, and the V/III ratio is 10. Under these conditions, the growth rate of InAs is 0.30 μm/h. Film forming is performed for about 36 seconds until the thickness of an InAs layer reaches 2 nm, and then the In and As beams are stopped. Next, after an interval of three seconds, Ga and Sb beams are emitted. In this step, the beam flux of Ga is 5.0×10.sup.−8 Torr, the beam flux of Sb is 5.0×10.sup.−7 Torr, and the V/III ratio is 10. Under these conditions, the growth rate of GaSb is 0.30 μm/h. Film forming is performed for about 36 seconds until the thickness of a GaSb layer reaches 2 nm, and then the Ga and Sb beams are stopped. After an interval of three seconds, the above steps are repeated. In this example, when the formation of an InAs layer and the formation of a GaSb layer constitute one cycle, the cycle is repeated 200 times to form the infrared absorption layer 115 with a total thickness of about 800 nm.
[0064] Next, the n-type contact layer 116 is formed on the infrared absorption layer 115. The n-type contact layer 116 is an n-type InAs layer that is formed by emitting In, As, and Si beams. In this step, the temperature of the Si cell is adjusted so that the concentration of Si that is an impurity element used as a dopant of the n-type contact layer 116 becomes 5.0×10.sup.18 cm.sup.−3. Also in this step, the beam flux of In is 5.0×10.sup.−8 Torr, the beam flux of As is 5.0×10.sup.7 Torr, and the V/III ratio is 10. Under these conditions, the growth rate of InAs is 0.30 μm/h. Film forming is performed for about 6 minutes until the thickness of an InAs layer reaches 30 nm, and then the In and Si beams are stopped.
[0065] Next, in a state where the As beam is being emitted, the substrate temperature is dropped to 400° C. Then, the As beam is stopped, and a structure where epitaxial films are formed on the GaSb substrate 111 is taken out of the vacuum chamber of the MBE apparatus.
[0066] Next, as illustrated by
[0067] Next, as illustrated by
[0068] Next, a photoresist is applied to the structure of
[0069] Next, as illustrated by
[0070] Next, as illustrated in
[0071] Configurations of the infrared detector not described above are substantially the same as those in the first embodiment.
Third Embodiment
[0072] Next, a third embodiment is described. In the third embodiment, a GaSb semiconductor laser produced by using the semiconductor crystal substrate of the first embodiment is described.
[0073] The semiconductor laser of the third embodiment includes the semiconductor crystal substrate of the first embodiment where the first GaSb layer 112 and the second GaSb layer 113 are sequentially formed on the GaSb substrate 111. The semiconductor laser also includes a p-type GaSb cladding layer 221, a multi-quantum well (MQW) layer 222, an n-type GaSb cladding layer 223, and an n-type InAs layer 224 that are formed on the second GaSb layer 113 in this order. The p-type GaSb cladding layer 221 has a thickness of about 500 nm and is doped with Be as a p-type impurity element. The MQW layer 222 is formed by alternately stacking a GaSb layer with a thickness of about 5 nm and an InAs layer with a thickness of about 5 nm. In the present embodiment, the MQW layer 222 includes 20 pairs of the GaSb layer and the InAs layer. The n-type GaSb cladding layer 223 has a thickness of about 100 nm, is doped with Si as an n-type impurity element, and has a carrier concentration of 5.0×10.sup.18 cm.sup.−3. The n-type InAs layer 224 has a thickness of about 30 nm.
[0074] Next, portions of the n-type InAs layer 224, the n-type GaSb cladding layer 223, and the MQW layer 222 are removed to form a mesa structure 230. Specifically, portions of the n-type InAs layer 224, the n-type GaSb cladding layer 223, and the MQW layer 222 are removed by dry etching using a CF.sub.4 gas as an etching gas to expose portions of the p-type GaSb cladding layer 221 and thereby form the mesa structure 230.
[0075] Next, lower electrodes 241 are formed on the exposed portions of the p-type GaSb cladding layer 221, and an upper electrode 242 is formed on the upper surface of the n-type InAs layer 224. Each of the lower electrodes 241 and the upper electrode 242 is formed of, for example, a metal multilayer film of Ti, Pt, and Au.
[0076] Then, the GaSb substrate 111 is cleaved to form a stripe-shaped piece having a width of 20 μm and a length of 50 μm. As a result, the semiconductor laser of the present embodiment is produced. The semiconductor laser is an edge emitting laser with a wavelength of 3.0 μm.
Fourth Embodiment
[0077] Next, a fourth embodiment is described. In the fourth embodiment, a GaSb light emitting diode (LED) produced by using the semiconductor crystal substrate of the first embodiment is described.
[0078] The light emitting diode of the fourth embodiment includes the semiconductor crystal substrate of the first embodiment. Similarly to the third embodiment, after the p-type GaSb cladding layer 221, the MQW layer 222, the n-type GaSb cladding layer 223, and the n-type InAs layer 224 are epitaxially grown on the second GaSb layer 113 by MBE, the lower electrode 241 and the upper electrode 242 are formed.
[0079] Then, the GaSb substrate 111 is cleaved to form a chip having a width of 50 μm and a length of 50 μm. As a result, the light emitting diode of the fourth embodiment is produced. The light emitting diode emits light from the side on which the n-type InAs layer 224 is formed. Accordingly, the area of the n-type InAs layer 224 where the upper electrode 242 is not present is preferably as large as possible.
Fifth Embodiment
[0080] Next, a fifth embodiment is described. In the fifth embodiment, a field effect transistor (FET) produced by using the semiconductor crystal substrate of the first embodiment is described.
[0081] The field effect transistor of the fifth embodiment includes the semiconductor crystal substrate of the first embodiment where the first GaSb layer 112 and the second GaSb layer 113 are sequentially formed on the GaSb substrate 111. An Al.sub.0.8Ga.sub.0.2Sb layer 251 and a channel layer 252 are sequentially formed by MBE on the second GaSb layer 113. The thickness of the Al.sub.0.8Ga.sub.0.2Sb layer 251 is about 2 nm. The channel layer 252 is a p-type In.sub.0.2Ga.sub.0.8Sb layer with a thickness of 5 nm, is doped with Be as a p-type impurity element, and has a carrier concentration of 5.0×10.sup.18 cm.sup.−3.
[0082] Next, an insulating film 260 is formed by atomic layer deposition (ALD) on the channel layer 252. The insulating film 260 is an Al.sub.2O.sub.3 film with a thickness of 3 nm.
[0083] Next, a gate electrode 271 is formed on the insulating film 260, and a source electrode 272 and a drain electrode 273 are formed on the channel layer 252. The gate electrode 271 may be a tungsten (W) film with a thickness of about 100 nm, and may be formed by CVD on the insulating layer 260. The gate electrode 271 is formed to have a gate length of 30 nm. Next, portions of the insulating film 260, which correspond to areas where the source electrode 272 and the drain electrode 273 are to be formed, are removed. Then, the source electrode 272 and the drain electrode 273 are formed in the areas with, for example, Ni films.
[0084] Through the above process, the field effect transistor of the fifth embodiment is produced.
Sixth Embodiment
[0085] Next, a sixth embodiment is described. In the sixth embodiment, a thermoelectric transducer produced by using the semiconductor crystal substrate of the first embodiment is described. The thermoelectric transducer of the sixth embodiment is described below with reference to
[0086] The thermoelectric transducer of the sixth embodiment includes the semiconductor crystal substrate of the first embodiment where the first GaSb layer 112 and the second GaSb layer 113 are sequentially formed on the GaSb substrate 111. A superlattice layer 280 and a cap layer 281 are sequentially formed by MBE on the second GaSb layer 113. The superlattice layer 280 is formed by alternately stacking a GaSb layer with a thickness of about 5 nm and an InAs layer with a thickness of about 5 nm. In the present embodiment, the superlattice layer 280 includes 500 pairs of the GaSb layer and the InAs layer. The cap layer 281 is a non-doped InAs film with a thickness of 30 nm.
[0087] Next, portions of the cap layer 281, the superlattice layer 280, the second GaSb layer 113, and the first GaSb layer 112 are removed to form mesa structures 282. Specifically, portions of the cap layer 281, the superlattice layer 280, the second GaSb layer 113, and the first GaSb layer 112 are removed by dry etching using a CF.sub.4 gas as an etching gas to form the mesa structures 282.
[0088] Next, an SiO.sub.2 film 283 is formed to fill a gap between the mesa structures 282. Next, the back side of the GaSb substrate 111 is ground by chemical mechanical polishing (CMP) to reduce the thickness of the GaSb substrate 111 to about 3 μm. Next, n-type and p-type dopants are ion-implanted into the mesa structures 282 and activation annealing is performed to form n-type regions (n-type elements) and p-type regions (p-type elements). Then, electrodes 290 are formed on the ends of the n-type elements and the p-type elements such that the n-type elements and the p-type elements are connected in series. Each of the electrodes 290 is formed of, for example, a metal multilayer film of Ti, Pt, and Au.
[0089] An aspect of this disclosure makes it possible to provide a semiconductor crystal substrate including a GaSb layer with a highly-flat surface.
[0090] All examples and conditional language provided herein are intended for the pedagogical purposes of aiding the reader in understanding the invention and the concepts contributed by the inventors to further the art, and are not to be construed as limitations to such specifically recited examples and conditions, nor does the organization of such examples in the specification relate to a showing of the superiority and inferiority of the invention. Although one or more embodiments of the present invention have been described in detail, it should be understood that the various changes, substitutions, and alterations could be made hereto without departing from the spirit and scope of the invention.