The present invention relates to a semiconductor wafer, an electronic device, and a method of manufacturing the semiconductor wafer. More particularly, the present invention relates to a semiconductor wafer, an electronic device, and a method of manufacturing the semiconductor wafer, in which a compound semiconductor crystal thin film having superior crystallinity is formed on an insulating film with the use of a low-cost Silicon-On-Insulator (SOT) wafer.
A variety of highly advanced electronic devices using heterojunctions are developed as electronic devices using GaAs-based or other compound semiconductor crystals. The performance of these electronic devices depends on the crystallinity of the compound semiconductor crystals. Therefore, high-quality crystal thin films are required. When electronic devices using GaAs-based compound semiconductor crystals are manufactured, a thin film is grown on a base wafer made of GaAs, or Ge whose lattice constant is very close to the lattice constant of GaAs, or the like due to requirements including the fact that a lattice match is necessary at the hetero interface.
Patent Document 1 discloses a semiconductor device that has a limited epitaxial region that is grown on a wafer having a lattice mismatch or a wafer having a high dislocation defect density. Non-Patent Document 1 discloses a low-dislocation-density GaAs epitaxial layer grown on a Ge-coated Si wafer by means of lateral epitaxial overgrowth. Non-Patent Document 2 discloses a technique to form, on a Si wafer, a Ge epitaxial growth layer (hereinafter, may be referred to as a Ge epilayer) with high-quality. According to this technique, the Ge epilayer is first formed on a limited region of the Si wafer and then subjected to thermal cycle annealing. This enables the Ge epilayer to achieve an average dislocation density of 2.3×106 cm−2.
Patent Document 1: JP 04-233720 A
Non-Patent Document 1: B. Y. Tsaur et al., “Low-dislocation-density GaAs epilayers grown on Ge-coated Si substrates by means of lateral epitaxial overgrowth,” Appl. Phys. Lett. 41(4)347-349, 15 Aug. 1982
Non-Patent Document 2: Hsin-Chiao Luan et al., “High-quality Ge epilayers on Si with low threading-dislocation densities,” APPLIED PHYSICS LETTERS, VOLUME 75, NUMBER 19, 8 Nov. 1999
GaAs-based electronic devices are preferably formed on wafers that can accomplish a lattice match with GaAs, for example, a GaAs wafer or a Ge wafer. However, the wafers that can accomplish a lattice match with GaAs, such as a GaAs wafer or a Ge wafer, are disadvantageously expensive. Furthermore, such wafers do not have sufficiently high heat dissipation characteristics. This necessitates reduction in the density of the devices for a relaxed thermal design. Therefore, good-quality semiconductor wafers are desired that are formed using low-cost Si wafers and have crystal thin films made of GaAs-based or other compound semiconductors. It is also desired to provide semiconductor wafers that can realize GaAs-based electronic devices with high-speed switching capabilities.
For a solution to the above-mentioned problems, according to the first aspect related to the present invention, provided is one exemplary semiconductor wafer including a base wafer, an insulating layer, and a Si crystal layer in the stated order. Here, the semiconductor wafer includes a seed crystal that is disposed on the Si crystal layer where the seed crystal has been subjected to annealing, and a compound semiconductor that has a lattice match or a pseudo lattice match with the seed crystal. The seed crystal is sized such that heat stress resulting from the annealing produces no defects therein. A boundary of the seed crystal, the boundary facing the compound semiconductor, has been surface-treated with a gaseous P compound. The compound semiconductor is a group III-V compound semiconductor or II-VI compound semiconductor. When the compound semiconductor is a group III-V compound semiconductor, the compound semiconductor may contain at least one among Al, Ga, and In as a group III element and at least one among N, P, As, and Sb as a group V element.
The semiconductor wafer may further include an inhibition layer that inhibits crystal growth of the compound semiconductor, and the inhibition layer may have an opening that penetrates therethrough to reach the Si crystal layer, and the seed crystal is disposed within the opening. In the semiconductor wafer, the inhibition layer may be formed on the Si crystal layer. A portion of the compound semiconductor, the portion being positioned within the opening, may have an aspect ratio of less than 12. The inhibition layer may be formed by thermally oxidizing a region of the Si crystal layer other than a region in which the seed crystal is disposed thereon.
The compound semiconductor may include a seed compound semiconductor crystal that is grown on the seed crystal to protrude above a surface of the inhibition layer, and a laterally-grown compound semiconductor crystal that is laterally grown along the inhibition layer from the seed compound semiconductor crystal serving as a nucleus. The laterally-grown compound semiconductor crystal may include a first compound semiconductor crystal that is laterally grown along the inhibition layer from the seed compound semiconductor crystal serving as a nucleus, and a second compound semiconductor crystal that is, in a different direction than that of the first compound semiconductor crystal, laterally grown along the inhibition layer from the first compound semiconductor crystal serving as a nucleus.
The Si crystal layer, the seed crystal, and the compound semiconductor may be formed substantially parallel to the base wafer. The semiconductor wafer may further include an inhibition layer that covers an upper plane of the Si crystal layer and inhibits crystal growth of the compound semiconductor. A plurality of seed crystals may be arranged on the Si crystal layer at equal intervals.
The semiconductor wafer may further include a defect trap that traps a defect produced in the seed crystal, and a maximum distance from any point in a region in the seed crystal to the defect trap may be shorter than a distance by which the defect can be moved by the annealing. The defect trap may be a region among a boundary of the seed crystal or a surface of the seed crystal, in which the compound semiconductor does not have a lattice match or a pseudo lattice match.
The seed crystal may include a grown SixGe1-x crystal (0≦x<1) or a GaAs that is grown at a temperature of 500° C. or lower. The compound semiconductor may include a buffer layer made of a group III-V compound semiconductor containing P, and the buffer layer may have a lattice match or a pseudo lattice match with the seed crystal.
The semiconductor wafer may further include a Si semiconductor device that is disposed on a portion of the Si crystal layer, the portion being not covered by the seed crystal. The base wafer may be made of single crystal Si, and the semiconductor wafer may further include a Si semiconductor device that is disposed on a portion of the base wafer, the portion being not covered by the seed crystal.
The seed crystal may have a dislocation density of 1×106/cm2 or less at a surface thereof. A plane of the Si crystal layer on which the seed crystal is formed may have an off angle with respect to any one crystal plane selected from among the (100) plane, the (110) plane, the (111) plane, a plane crystallographically equivalent to the (100) plane, a plane crystallographically equivalent to the (110) plane, and a plane crystallographically equivalent to the (111) plane. The off angle may be no less than 2° and no more than 6°.
The seed crystal may have a bottom area of 1 mm2 or less. The seed crystal may have a bottom area of 1600 μm2 or less. The seed crystal may have a bottom area of 900 μm2 or less.
The seed crystal may have a bottom a maximum width of which is 80 μm or less. The seed crystal may have a bottom a maximum width of which is 40 μm or less.
The base wafer may have a main plane that has an off angle with respect to the (100) plane or a plane crystallographically equivalent to the (100) plane, the seed crystal may have a bottom shaped as a rectangle, and one of the sides of the rectangle may be substantially parallel to any one of the <010> direction, the <0-10> direction, the <001> direction, and the <00-1> direction of the base wafer. In this case, the off angle may be also no less than 2° and no more than 6°.
The base wafer may have a main plane that has an off angle with respect to the (111) plane or a plane crystallographically equivalent to the (111) plane, the seed crystal may have a bottom shaped as a hexagon, and one of the sides of the hexagon may be substantially parallel to any one of the <1-10> direction, the <−110> direction, the <0-11> direction, the <01-1> direction, the <10-1> direction, and the <−101> direction of the base wafer. In this case, the off angle may be also no less than 2° and no more than 6°.
The inhibition layer may have a maximum outer width of 4250 μm or less. The inhibition layer may have a maximum outer width of 400 μm or less.
According to the second aspect related to the present invention, provided is one exemplary electronic device including a wafer, an insulating layer that is formed on the wafer, a Si crystal layer that is formed on the insulating layer, a seed crystal that is formed on the Si crystal layer, the seed crystal having been subjected to annealing, a compound semiconductor that has a lattice match or a pseudo lattice match with the seed crystal, and a semiconductor device formed using the compound semiconductor.
The electronic device may further include an inhibition layer that inhibits crystal growth of the compound semiconductor. Here, the inhibition layer may have an opening that penetrates therethrough to reach the Si crystal layer, the seed crystal may be positioned within the opening, and the compound semiconductor may include a seed compound semiconductor crystal that is grown on the seed crystal to protrude above a surface of the inhibition layer and a laterally-grown compound semiconductor crystal that is laterally grown along the inhibition layer from the seed compound semiconductor crystal serving as a nucleus.
According to the third aspect related to the present invention, one exemplary method of producing a semiconductor wafer is provided. The method includes a step of providing an SOI wafer that has a base wafer, an insulating layer and a Si crystal layer in the stated order, a step of growing a seed crystal on the Si crystal layer, a step of annealing the seed crystal, and a step of growing a compound semiconductor that has a lattice match or a pseudo lattice match with the seed crystal. The step of growing a seed crystal includes a step of forming, on the Si crystal layer, an inhibition layer that inhibits the crystal growth of the compound semiconductor, a step of forming, in the inhibition layer, an opening that penetrates through the inhibition layer to reach the Si crystal layer, and a step of growing the seed crystal within the opening. The step of growing a seed crystal includes growing a plurality of the seed crystals at equal intervals. The step of growing a seed crystal includes growing the seed crystal to be sized such that heat stress resulting from the step of annealing produces no defects in the seed crystal. The step of annealing is performed with a temperature and a duration being set such that a defect in the seed crystal can be moved to an outer edge of the seed crystal. The method may include a step of performing the step of annealing multiple times. The step of annealing may enable the seed crystal to have a dislocation density of 1×106/cm2 or less at a surface thereof.
The method may further include, prior to the step of growing a compound semiconductor, a step of forming an inhibition layer that inhibits the crystal growth of the compound semiconductor by thermally oxidizing a region of the Si crystal layer other than a region in which the seed crystal is formed thereon.
Some aspects of the invention will now be described based on the embodiments, which do not intend to limit the scope of the present invention, but exemplify the invention. All of the features and the combinations thereof described in the embodiment are not necessarily essential to the invention.
In at least part of the semiconductor wafer 10, the base wafer 12, the insulating layer 13, the Si crystal layer 14, and the seed crystal 16 are arranged in the stated order in a substantially perpendicular direction to a main plane 11 of the base wafer 12. Thus, the insulating layer 13 insulates the base wafer 12 and the Si crystal layer 14 from each other so as to reduce leakage currents flowing into the base wafer 12. As used herein, “a substantially perpendicular direction” refers not only to a strictly perpendicular direction but also to directions slightly off the perpendicular direction considering the manufacturing errors of the wafer and the respective components.
The base wafer 12 is a silicon wafer, for example. The insulating layer 13 is a silicon oxide layer that is formed by oxidizing the main plane 11 of the base wafer 12, for example. The Si crystal layer 14 is a layer of single crystal silicon formed on the insulating layer 13, for example. The base wafer 12, the insulating layer 13, and the Si crystal layer 14 may constitute a commercially available SOI wafer.
The seed crystal 16 and the compound semiconductor 18 are epitaxially grown on the Si crystal layer 14 by metal organic chemical vapor deposition (MOCVD) or molecular beam epitaxy (MBE) using organic metals as the source. The seed crystal 16 includes a SixGe1-x crystal (0≦x<1) or a GaAs crystal that is formed at the temperature of 500° C. or lower.
The seed crystal 16 is subjected to annealing. The seed crystal 16 may be subjected to annealing in the state of being formed on the Si crystal layer 14. The seed crystal 16 is subjected to annealing at the temperature lower than 900° C., preferably 850 C.° or lower. This can maintain the surface of the seed crystal 16 planar. The seed crystal 16 may be alternatively subjected to annealing at the temperature of 680° C. or higher, preferably 700 C.° or higher. This can reduce the density of the crystal defects in the seed crystal 16.
The annealing may be performed multiple times. For example, high-temperature annealing is first performed at the temperature lower than the melting point of Ge, between 800° C. and 900° C., for 2 to 10 minutes, and low-temperature annealing is then performed at the temperature between 680° C. and 780° C. for 2 to 10 minutes. These annealing operations can reduce the density of the defects in the seed crystal 16.
The seed crystal 16 may be subjected to annealing under the atmospheric, nitrogen, argon, or hydrogen atmosphere. In particular, subjecting the seed crystal 16 to annealing under the hydrogen-containing atmosphere can reduce the density of the crystal defects in the seed crystal 16 while maintaining the smooth surface of the seed crystal 16.
As used herein, the term “a pseudo lattice match” indicates the state in which two semiconductors can be stacked together in contact with each other without a perfect lattice match but only a small difference exists between the lattice constants of the two semiconductors in contact with each other and the lattice mismatch produces no significant defects. The difference between the lattice constants is absorbed by elastic deformation of the crystal lattices of the respective semiconductors. For example, a pseudo lattice match may be established between Ge and GaAs, or between Ge and InGaP when the two different semiconductors are stacked together without violating the thickness requirements imposed by lattice relaxation.
The compound semiconductor 18 has a lattice match or a pseudo lattice match with the annealed seed crystal 16. The compound semiconductor 18 is a crystal grown by using the seed crystal 16 as a nucleus. The use of the annealed seed crystal 16 enables the compound semiconductor 18 to have excellent crystallinity. The compound semiconductor 18 is, for example, a group III-V compound semiconductor or group II-VI compound semiconductor. When the compound semiconductor 18 is a group III-V compound semiconductor, the compound semiconductor 18 may contain at least one among Al, Ga, and In as the group III element and at least one among N, P, As, and Sb as the group V element.
For example, the insulating layer 13 is smaller in area than the base wafer 12. For example, the Si crystal layer 14 is smaller in area than the insulating layer 13. For example, the seed crystal 16 and the compound semiconductor 18 are smaller in area than the Si crystal layer 14. In the present embodiment, the case where the seed crystal 16 and the compound semiconductor 18 are arranged in the substantially perpendicular direction to the main plane 11 of the base wafer 12 has been explained. Alternatively, however, the seed crystal 16 and the compound semiconductor 18 may be arranged in a substantially parallel direction to the main plane 11 of the base wafer 12.
In the present embodiment, the case where the base wafer 12 and the insulating layer 13 are in contact with each other has been explained. However, the positional relation between the base wafer 12 and the insulating layer 13 is not limited to such. There may be one or more different layers between the base wafer 12 and the insulating layer 13. In the present embodiment, the case where the Si crystal layer 14 and the seed crystal 16 are in contact with each other has been explained. However, the positional relation between the Si crystal layer 14 and the seed crystal 16 is not limited to such. There may be one or more different layers between the Si crystal layer 14 and the seed crystal 16. Furthermore, the seed crystal 16 and the compound semiconductor 18 each may be constituted by a plurality of crystal layers.
The inhibition layer 25 is formed on the Si crystal layer 14. The inhibition layer 25 inhibits at least the crystal growth of the compound semiconductor 28. The inhibition layer 25 may further inhibit the crystal growth of the seed crystal 26. The inhibition layer 25 has an opening 27 penetrating therethrough from the surface of the inhibition layer 25 to the Si crystal layer 14 in the substantially perpendicular direction to the main plane 11 of the base wafer 12.
In this way, a crystal is not grown on the surface of the inhibition layer 25 and instead selectively grown within the opening 27. For example, the inhibition layer 25 is smaller in area than the Si crystal layer 14. The inhibition layer 25 may be made of SiO2 and formed by, for example, CVD. The opening 27 may be formed by photolithography.
The seed crystal 26 and the compound semiconductor 28 are equivalent to the seed crystal 16 and the compound semiconductor 18 described with reference to
As described above, the seed crystal 26 is subjected to annealing. This reduces the density of the defects in the seed crystal 26. The compound semiconductor 28 has a lattice match or a pseudo lattice match with the seed crystal 26. The use of the annealed seed crystal 26 enables the compound semiconductor 28 to have excellent crystallinity.
The semiconductor wafer 30 is different from the semiconductor wafer 10 in that the Si crystal layer 34, the seed crystal 36, and the compound semiconductor 38 are arranged in the substantially parallel direction to the main plane 11 of the base wafer 12. The Si crystal layer 34, the seed crystal 36, and the compound semiconductor 38 are arranged in the stated order along a surface 19 of the insulating layer 13. In other words, the seed crystal 36 is disposed between the Si crystal layer 34 and the compound semiconductor 38.
The Si crystal layer 34, the seed crystal 36, and the compound semiconductor 38 are each smaller in area than the insulating layer 13. In the present embodiment, the seed crystal 36 and the compound semiconductor 38 are arranged in the substantially parallel direction to the main plane 11 of the base wafer 12. Alternatively, however, the seed crystal 36 and the compound semiconductor 38 may be arranged in the substantially perpendicular direction to the main plane 11 of the base wafer 12. As used herein, “a substantially parallel direction” refers not only to a strictly parallel direction but also to directions slightly off the parallel direction considering the manufacturing errors of the wafer and the respective components.
The semiconductor wafer 40 is different from the semiconductor wafer 30 in terms of further including the inhibition layer 45 that covers an upper plane 43 of the Si crystal layer 44. The upper plane 43 of the Si crystal layer 44 is a plane that faces away from the base wafer 12 among planes being substantially parallel to the main plane 11 of the base wafer 12. The inhibition layer 45 inhibits the crystal growth of the compound semiconductor 48 and the seed crystal 46.
In this way, the seed crystal 46 is selectively grown by using as a nucleus a lateral plane 41 of the Si crystal layer 44, the plane 41 being substantially perpendicular to the main plane 11 of the base wafer 12. This improves the crystallinity of the seed crystal 46. The insulating layer 13 may include a material that inhibits the crystal growth. For example, the insulating layer 13 is made of SiO2.
The semiconductor wafer 40 can be manufactured according to the following procedure. To begin with, an SDI wafer is prepared which includes the base wafer 12, the insulating layer 13, and a Si crystal layer. The Si crystal layer of the SOT wafer is then patterned by etching or the like into a rectangular Si crystal layer. After this, the inhibition layer 45 is formed so as to cover a plane substantially parallel to the main plane 11 of the base wafer 12 among planes of the rectangular Si crystal layer. The inhibition layer 45 may have a similar shape to the rectangular Si crystal layer. The inhibition layer 45 is formed by depositing SiO2 by CVD, for example. The rectangular Si crystal layer is then subjected to etching, so that the Si crystal layer 44 is formed. Since the Si crystal layer 44 resulting from the etching is smaller than the inhibition layer 45, a space is provided between the inhibition layer 45 and the insulating layer 13.
Following this, the seed crystal 46 is selectively grown on the plane 41 of the Si crystal layer 44, the plane 41 being substantially perpendicular to the main plane 11 of the base wafer 12. The seed crystal 46 is formed by, for example, MOCVD. Subsequently, the seed crystal 46 is subjected to annealing. The annealing improves the crystallinity of the seed crystal 46. After this, the compound semiconductor 48 is formed which has a lattice match or a pseudo lattice match with the seed crystal 46. The compound semiconductor 48 is formed by, for example, CVD.
The Ge crystal layer 106 is equivalent to the seed crystal 16, the seed crystal 26, the seed crystal 36, or the seed crystal 46. The seed compound semiconductor crystal 108, the first compound semiconductor crystal 110, and the second compound semiconductor crystal 112 are each equivalent to the compound semiconductor 18, the compound semiconductor 28, the compound semiconductor 38, or the compound semiconductor 48. The following may not repeat the same description about the equivalent components.
In the present example, the Ge crystal layer 106, which is disposed within an opening 105, is used as a nucleus to grow the seed compound semiconductor crystal 108 until it projects from the opening 105. The seed compound semiconductor crystal 108 is then used as a nucleus to grow the first compound semiconductor crystal 110 in a first direction on the surface of the inhibition layer 104. The first compound semiconductor crystal 110 is then used as a nucleus to grow the second compound semiconductor crystal 112 in a second direction on the surface of the inhibition layer 104. Here, the first direction perpendicularly intersects the second direction, for example.
The electronic device 100 may include a plurality of metal insulator semiconductor field effect transistors (MISFETs) or high electron mobility transistors (HEMTs).
In at least part of the SOI wafer 102, the Si wafer 162, the insulating layer 164, and the Si crystal layer 166 are arranged in the stated order. The SOI wafer 102 has the insulating layer 164 and the Si crystal layer 166 on the side of a main plane 172 of the Si wafer 162. The Si wafer 162 may be a single crystal Si wafer. The Si wafer 162 serves as the wafer of the electronic device 100.
The insulating layer 164 electrically insulates the Si wafer 162 and the Si crystal layer 166 from each other. The insulating layer 164 is in contact with the main plane 172 of the Si wafer 162. The Si crystal layer 166 may contain Si single crystals. The Si crystal layer 166 is in contact with the insulating layer 164. The Si wafer 162 and the insulating layer 164 are equivalent to the base wafer 12 and the insulating layer 13. The Si crystal layer 166 is equivalent to the Si crystal layer 14, the Si crystal layer 34, or the Si crystal layer 44. The following may not repeat the same description about the equivalent components.
Active elements such as MISFETs or HEMTs are formed on the SOI wafer 102. When the electronic device 100 is formed on the SOI wafer 102, the electronic device 100 achieves a reduced stray capacitance, thereby being capable of operating faster. The insulating layer 164, which provides a high insulation resistance, can prevent the leakage currents from flowing into the Si wafer 162 from the electronic device 100.
The inhibition layer 104 is formed in contact with the Si crystal layer 166 on the side of the main plane 172 of the SOI wafer 102. The inhibition layer 104 is equivalent to the inhibition layer 25 or the inhibition layer 45. The inhibition layer 104 has an opening 105 that penetrates therethrough in the substantially perpendicular direction to the main plane 172 of the Si wafer 162. The inhibition layer 104 inhibits the epitaxial growth of the seed compound semiconductor crystal 108, the first compound semiconductor crystal 110, and the second compound semiconductor crystal 112.
The opening 105 externally exposes the Si crystal layer 166 before the seed compound semiconductor crystal 108 is formed. Stated differently, the inhibition layer 104 has the opening 105 that extends from the surface of the inhibition layer 104 to the Si crystal layer 166. Accordingly, an epitaxial film is selectively grown within the opening 105, in which the Si crystal layer 166 is exposed. For example, the Ge crystal layer 106 is selectively grown within the opening 105. Furthermore, the Ge crystal layer 106 is used as a nucleus to selectively grow the seed compound semiconductor crystal 108 within the opening 105. On the other hand, no epitaxial film is grown on the surface of the inhibition layer 104 since crystal growth is inhibited on the surface of the inhibition layer 104. The inhibition layer 104 may contain silicon oxide or silicon nitride.
As used herein, “an aspect ratio of an opening” is defined as a result of dividing “the depth of the opening” by “the width of the opening.” For example, an aspect ratio is defined as the result of dividing the etching depth by the pattern width in “Handbook for Electronics, Information and Communication Engineers, Volume 1,” edited by the Institute of Electronics, Information and Communication Engineers, Page 751, 1988, published by Ohmsha. The term “aspect ratio” is used herein to mean a similar meaning to the above. The depth of the opening is defined as the depth of the opening in the direction in which the thin films are stacked on the wafer. The width of the opening is defined as the width of the opening in the perpendicular direction to the stacking direction. When the opening has a varying width, the width of the opening is defined as the minimum width of the opening. For example, when the opening is shaped as a rectangle when seen in the stacking direction, the width of the opening is defined as the length of the short side of the rectangle.
When the Ge crystal layer 106 is grown within the opening 105, the depth of the opening 105 is defined as the distance between the surface of the Ge crystal layer 106 and the surface of the inhibition layer 104. When the seed compound semiconductor crystal 108 is selectively grown by using the Ge crystal layer 106 as a nucleus, the depth of the opening 105 is defined as a portion of the seed compound semiconductor crystal 108, the portion being positioned within the opening 105. Here, the portion of the seed compound semiconductor crystal 108 that is positioned within the opening 105 refers to the perpendicular width of the seed compound semiconductor crystal 108 from the level of the surface of the Ge crystal layer 106 to the level of the surface of the inhibition layer 104. Accordingly, the aspect ratio of the opening 105 is herein defined as the result of dividing the height of the portion of the seed compound semiconductor crystal 108 which is positioned within the opening 105 by the width of the opening.
When the Ge crystal layer 106 formed within the opening 105 is not heated to the temperature around 600 to 900° C., the opening 105 preferably has an aspect ratio of √3/3 or higher, for example. More specifically, when the Si crystal layer 166 has a plane orientation (100) at the bottom of the opening 105, the opening 105 may have an aspect ratio of 1 or higher. When the Si crystal layer 166 has a plane orientation (111) at the bottom of the opening 105, the opening 105 may have an aspect ratio of √2 (=approximately 1.414) or higher. When the Si crystal layer 166 has a plane orientation (110) at the bottom of the opening 105, the opening 105 may have an aspect ratio of √3/3 (=approximately 0.577) or higher.
When the Ge crystal layer 106 is formed within the opening 105 having an aspect ratio of √3/3 or higher, the defects in the Ge crystal layer 106 are terminated by the wall of the opening 105. This reduces the defects on the surface of the Ge crystal layer 106, the surface being not covered by the wall of the opening 105 and thus externally exposed. Thus, when the opening 105 has an aspect ratio of √3/3 or higher, even if the Ge crystal layer 106 formed within the opening 105 is not subjected to annealing, the density of the defects on the surface of the Ge crystal layer 106 that is externally exposed through the opening 105 can be lowered to fall within a prescribed acceptable range. The use of the surface of the Ge crystal layer 106 that is exposed through the opening 105 as a nucleus of the seed compound semiconductor crystal 108 can enhance the crystallinity of the seed compound semiconductor crystal 108.
When it is possible to heat the Ge crystal layer 106 formed within the opening 105 to the temperature around 600 to 900° C. to anneal the Ge crystal layer 106, the opening 105 may be allowed to have an aspect ratio of less than √2. The opening 105 is allowed to have an aspect ratio of less than √2 since annealing can complementarily reduce the defects in the Ge crystal layer 106. More specifically, when the Si crystal layer 166 has a plane orientation (100) at the bottom of the opening 105, the opening 105 may have an aspect ratio of less than 1. When the Si crystal layer 166 has a plane orientation (111) at the bottom of the opening 105, the opening 105 may have an aspect ratio of less than √2 (=approximately 1.414) or higher. When the Si crystal layer 166 has a plane orientation (110) at the bottom of the opening 105, the opening 105 may have an aspect ratio of less than √3/3 (=approximately 0.577) or higher. The Ge crystal layer 106 may be subjected to annealing before any compound semiconductor crystal is grown on the Ge crystal layer 106.
The opening 105 may have a bottom area of 1 mm2 or smaller, preferably less than 0.25 mm2. In this case, the seed compound semiconductor crystal 108 also has a bottom area of 1 mm2 or smaller, or 0.25 mm2. When the seed compound semiconductor crystal 108 is sized equal to or smaller than a prescribed size, performing annealing under prescribed conditions can move a defect at any point within the seed compound semiconductor crystal 108 to the edge of the seed compound semiconductor crystal 108. Thus, the defect density of the seed compound semiconductor crystal 108 can be easily lowered.
The opening 105 may have a bottom area of 0.01 mm2 or smaller, preferably 1600 μm2 or smaller, more preferably 900 μm2 or smaller. In these cases, the seed compound semiconductor crystal 108 formed within the opening 105 similarly has a bottom area of 0.01 mm2 or smaller, 1600 μm2 or smaller, or 900 μm2 or smaller.
When there is a large difference in thermal expansion coefficient between the SDI wafer 102 and a functional layer such as the seed compound semiconductor crystal 108 and a compound semiconductor layer, thermal annealing is highly likely to locally bend the functional layer. When the bottom area of the opening 105 is 0.01 mm2 or smaller, the duration required to anneal the Ge crystal layer 106 formed within the opening 105 can be made shorter than when the bottom area of the opening 105 is larger than 0.01 mm2. Thus, the opening 105 having a bottom area of 0.01 mm2 or smaller can reduce the crystal defects that may be generated in the functional layer by the bend.
When the opening 105 has a bottom area of larger than 1600 μm2, crystal defects cannot be sufficiently reduced and the semiconductor wafer is thus not likely to have prescribed characteristics necessary to manufacture devices. When the opening 105 has a bottom area of 1600 μm2 or smaller, the number of crystal defects may be reduced to become equal to or fall below a prescribed number. If such is the case, the functional layer formed within the opening can be used to manufacture a high-performance device. When the bottom area of the opening 105 is 900 μm2 or smaller, the number of crystal defects is more likely to be reduced to become equal to or fall below a prescribed number and the manufacturing yield of the devices can be improved.
On the other hand, the opening 105 preferably has a bottom area of 25 μm2 or larger. The bottom area of smaller than 25 μm2 destabilizes the growth rate of the crystal epitaxially grown within the opening 105 and is likely to impair the shape of the crystal. The bottom area of smaller than 25 μm2 may also make it difficult to process the compound semiconductor formed within the opening 105 into a device and thus lower the yield.
The ratio of the bottom area of the opening 105 to the area of a covering region is preferably 0.01% or higher. Here, the covering region is defined as a region in which the inhibition layer 104 covers the Si crystal layer 166. The above ratio of lower than 0.01% destabilizes the rate at which a crystal is grown within the opening 105. When a plurality of openings 105 are formed in a single covering region, the bottom areas of the openings 105 in the covering region are summed together so that the total bottom area is used in calculating the above ratio.
The bottom of the opening 105 may be shaped such that the maximum width is 100 μm or smaller, preferably 80 μm or smaller. The maximum width of the bottom of the opening 105 is defined as the length of the longest straight line between any two points of the bottom of the opening 105. When the bottom of the opening 105 is shaped as a square or rectangle, the length of the side of the bottom may be 100 μm or smaller, preferably 80 μm or smaller. When the maximum width of the bottom is 100 μl or smaller, the Ge crystal layer 106 formed within the opening 105 can be annealed within a shorter duration than when the maximum width of the bottom is larger than 100 μm.
The Ge crystal layer 106 may be sized such that no defects are generated in the Ge crystal layer 106 even when stress occurs due to the difference in thermal expansion coefficient at the annealing temperature between the Ge crystal layer 106 and the Si crystal layer 166. For example, the maximum width of the Ge crystal layer 106 in the substantially parallel direction to the main plane 172 may be 40 μm or smaller, preferably 20 μm or smaller. Since the maximum width of the Ge crystal layer 106 is dependent on the maximum width of the bottom of the opening 105, the maximum width of the bottom of the opening 105 is preferably no more than a prescribed value. For example, the maximum width of the bottom of the opening 105 may be 40 μm or smaller, more preferably 30 μm or smaller.
A single opening 105 may be formed in a single inhibition layer 104. In this way, a crystal can be epitaxially grown at a stable rate within the opening 105. Alternatively, a plurality of openings 105 may be formed in a single inhibition layer 104. In this case, the openings 105 are preferably arranged at equal intervals. In this way, a crystal can be epitaxially grown at a stable rate within the openings 105.
When the bottom of the opening 105 is shaped as a polygon, at least one among the sides of the polygon preferably extends substantially in parallel to one of the crystallographic plane orientations of the main plane of the SOI wafer 102. The shape of the bottom of the opening 105 and the crystallographic plane orientations of the main plane of the SOI wafer 102 are preferably determined in relation to each other such that the crystal grown within the opening 105 has a stable lateral plane. Here, the expression “substantially parallel” includes a case where one of the sides of the polygon extends in a direction at a slight angle with respect to one of the crystallographic plane orientations of the wafer. The angle is, for example, 5° or smaller. This configuration can reduce disturbances in the crystal growth and contributes to stable growth of the crystal. Therefore, a well-shaped seed crystal can be obtained, which helps easy crystal growth.
The main plane of the SOI wafer 102 may be one of the (100) plane, the (110) plane and the (111) plane, or crystallographically equivalent to these planes. The main plane of the SOI wafer 102 is preferably at a slight angle with respect to the above-listed crystallographic plane orientations. Stated differently, the SIO wafer 102 preferably has an off angle. The angle may be 10° or smaller. The angle may be no less than 0.05° and no more than 6′, no less than 0.3° no more than 6°, no less than 2° and no more than 6°. When a rectangular crystal is grown within the opening, the main plane of the wafer may be one of the (100) plane and the (110) plane, or crystallographically equivalent to these planes. In this way, the crystal is more likely to have lateral planes related by 4-fold symmetry.
An exemplary case is described where the inhibition layer 104 is formed on the (100) plane of the surface of the SOI wafer 102, the opening 105 has a bottom shaped as a square or rectangle, the Ge crystal layer 106 is made of a Ge crystal, and the seed compound semiconductor crystal 108 is a GaAs crystal. In this case, at least one among the sides of the bottom shape of the opening 105 may extend in a direction substantially parallel to any one of the <010> direction, the <0-10> direction, the <001> direction, and the <00-1> direction of the SOI wafer 102. In this way, the GaAs crystal has stable lateral planes.
Another exemplary case is described where the inhibition layer 104 is formed on the (111) plane of the surface of the SOI wafer 102, the opening 105 has a bottom shaped as a hexagon, the Ge crystal layer 106 is made of a Ge crystal, and the seed compound semiconductor crystal 108 is a GaAs crystal. In this case, at least one among the sides of the bottom shape of the opening 105 may extend in a direction substantially parallel to any one of the <1-10> direction, the <−110> direction, the <0-11> direction, the <01-1> direction, the <10-1> direction, and the <−101> direction of the SOI wafer 102. In this way, the GaAs crystal has stable lateral planes. The bottom of the opening 105 may be shaped as a regular hexagon.
A plurality of inhibition layers 104 may be formed on the SOI wafer 102. In this case, the SOI wafer 102 has a plurality of covering regions formed thereon. For example, the inhibition layer 104 of
The seed compound semiconductor crystal 108 is grown within the opening 105 by chemical vapor deposition (CVD) or vapor phase epitaxy (VPE). According to these techniques, a source gas containing component elements of a thin-film crystal to be formed is supplied onto a wafer and a thin film is formed by vapor-phase chemical reaction of the source gas or chemical reaction of the source gas at the surface of the wafer. When supplied into a reactor, the source gas produces intermediates (hereinafter, may be referred to as precursors) in gas phase reactions. The produced intermediates diffuse in the gas phase to adsorb onto the surface of the wafer. The intermediates that have adsorbed onto the surface of the wafer undergo surface diffusion on the surface of the wafer, to be formed into a solid film.
Here, a sacrificial growth portion may be formed on the SOI wafer 102 between two adjacent inhibition layers 104. The sacrifice grown portion adsorbs the source of the Ge crystal layer 106 or the seed compound semiconductor crystal 108 to form a thin film at a higher rate than any of the upper planes of the two inhibition layers 104. The thin film deposited on the sacrificial growth portion does not need to have equal crystalline quality to the Ge crystal layer 106 or the seed compound semiconductor crystal 108 and may be a polycrystal or amorphous body. The thin film deposited on the sacrificial growth portion may not be used to manufacture devices.
The sacrificial growth portion may separately surround each inhibition layer 104. In this way, a crystal can be epitaxially grown at a stable rate within the opening 105.
Each inhibition layer 104 may have a plurality of openings 105. The electronic device 100 may have a sacrificial growth portion formed between two adjacent openings 105. The sacrificial growth portions may be arranged at equal intervals.
A region of the SOI wafer 102 that is in the vicinity of its surface may serve as the sacrificial growth portion. Alternatively, a groove that is formed in the inhibition layer 104 so as to penetrate through the inhibition layer 104 down to the SOI wafer 102 may serve as the sacrificial growth portion. The groove may have a width of no less than 20 μm and no more than 500 μm. It should be noted that crystal growth may also take place in the sacrificial growth portion.
As described above, the sacrificial growth portion is positioned between two adjacent inhibition layers 104. Furthermore, the sacrificial growth portion surrounds each inhibition layer 104. In this way, the sacrificial growth portion traps, adsorbs, or seizes the precursors that are diffused on the surface of the covering region. Therefore, a crystal can be grown at a stable rate within the opening 105. The precursors are an exemplary source for the seed compound semiconductor crystal 108.
For example, the surface of the SOI wafer 102 is externally exposed in a region other than the covering region in which the covering regions of a prescribed size are formed on the surface of the SOI wafer 102. When a crystal is grown within the opening 105 by MOCVD, some of the precursors that have reached the surface of the SOI wafer 102 are grown into a crystal on the surface of the SOI wafer 102. Since some of the precursors are consumed on the surface of the SOT wafer 102 as described above, a crystal is grown at a stable rate within the opening 105.
As yet another example, a semiconductor region made of Si, GaAs, or the like serves as the sacrificial growth portion. For example, the sacrificial growth portion is formed on the surface of the inhibition layer 104 by depositing an amorphous or polycrystalline semiconductor with ion plating, sputtering or the like. The sacrificial growth portion may be positioned between two adjacent inhibition layers 104 or included in the inhibition layer 104. Alternatively, a region may be provided between two adjacent covering regions that inhibits the diffusion of the precursors. The covering region may be surrounded by a region that inhibits the diffusion of the precursors.
As long as a slight distance is provided between two adjacent inhibition layers 104, a crystal is grown at a stable rate within the opening 105. Two adjacent inhibition layers 104 may be spaced away from each other by 20 μm or greater. Two adjacent inhibition layers 104 may be spaced away from each other by 20 μm or greater with a sacrificial growth portion provided therebetween. In this way, a crystal is grown at a more stable rate within the opening 105. Here, the distance between two adjacent inhibition layers 104 is defined as the minimum distance between a point on the periphery of one of the two inhibition layers 104 and a point on the periphery of the other. The inhibition layers 104 may be arranged at equal intervals. In particular, when two adjacent inhibition layers 104 are spaced away from each other by a distance less than 10 μm, a crystal can be grown at a stable rate within the opening 105 by arranging a plurality of inhibition layers 104 at equal intervals.
The SOI wafer 102 may be a high-resistance wafer without impurities or a low-resistance wafer with p- or n-type impurities. The Ge crystal layer 106 may be made of Ge without impurities or Ge with p- or n-type impurities.
When seen in the stacking direction, the opening 105 has any shape such as square, rectangular, circular, elliptical, oval and other shapes. When the opening 105 is shaped as a circle or ellipse when seen in the stacking direction, the diameter of the circle or the minor axis of the ellipse is referred to as the width of the opening 105. Furthermore, when taken along a plane parallel to the stacking direction, the cross-section of the opening 105 also has any shape such as rectangular, trapezoidal, parabolic, hyperbolic, and other shapes. When the cross-section of the opening 105 that is taken along a plane parallel to the stacking direction is shaped as a trapezoid, the minimum width at the bottom or entrance of the opening 105 is referred to as the width of the opening 105.
When shaped as a rectangle or square when seen in the stacking direction and as a rectangle when seen in cross section that is taken along a plane parallel to the stacking direction, the internal space defined within the opening 105 is three-dimensionally shaped as a cuboid. Here, it should be noted that the internal space defined within the opening 105 is three-dimensionally shaped in any manner. When the internal space defined within the opening 105 is three-dimensionally shaped in any manner other than as a cuboid, the aspect ratio of a cuboid that approximates the three-dimensional shape of the internal space defined within the opening 105 may be used as the aspect ratio of the three-dimensional shape.
The Ge crystal layer 106 may have a defect trap that traps defects, which move within the Ge crystal layer 106. The defects may include defects that are present when the Ge crystal layer 106 is formed. The defect trap may be a plane among a crystal boundary of the Ge crystal layer 106 or a crystal surface of the Ge crystal layer 106, or a flaw physically formed in the Ge crystal layer 106. For example, the defect trap is a plane among a crystal boundary or a crystal surface, the plane having a direction that is not substantially parallel to the Si wafer 162. For example, the defect trap is formed by etching the Ge crystal layer 106 into lines or discrete islands to form a crystal boundary in the Ge crystal layer 106. Alternatively, the defect trap is also formed by physically damaging the Ge crystal layer 106 by means of mechanical scratching, friction, ion implantation or the like. The defect trap is formed in a region of the Ge crystal layer 106, the region being not exposed by the opening 105. The defect trap may be a boundary between the Ge crystal layer and the inhibition layer 104.
The defect trap may be positioned so as to be away from any point in the Ge crystal layer 106 by a distance that is equal to or shorter than the distance by which defects can move by annealing that is carried out at a prescribed temperature for a prescribed duration. The distance L [μm] by which defects can move may be between 3 μm and 20 μm when annealing is performed at the temperature of 700 to 950° C. The defect trap may be positioned within the above-defined distance from every defect in the Ge crystal layer 106. In this manner, the annealing can reduce the threading defect density (or also referred to as the threading dislocation density) within the Ge crystal layer 106. For example, the threading dislocation density at the surface of the Ge crystal layer 106, which is shown as an exemplary seed crystal layer, is reduced to 1×106/cm2 or lower.
The annealing of the Ge crystal layer 106 may be carried out with the temperature and the duration being set such that the defects that are present when the Ge crystal layer 106 is formed can move to the defect trap of the Ge crystal layer 106. For example, when the outer edge of the Ge crystal layer 106 serves as the defect trap, the annealing may be performed with the temperature and the time of period being set such that a defect at any point within the Ge crystal layer 106 can move to the outer edge of the Ge crystal layer 106. The Ge crystal layer 106 may be sized such that the density of the defects within the Ge crystal layer 106 may be reduced by the annealing-induced movement of the defects that are present when the Ge crystal layer 106 is formed. The Ge crystal layer 106 may be formed such that the maximum width does not exceed double the distance by which defects may move when annealing is performed under prescribed conditions.
With the above-described configuration, the density of the defects is reduced in a region of the Ge crystal layer 106 excluding the defect trap. For example, when the Ge crystal layer 106 is epitaxially grown, lattice defects and the like may occur. The defects can move within the Ge crystal layer 106. As the temperature of the Ge crystal layer 106 increases, the movement speed also increases. Furthermore, the defects are trapped by the surface, the boundary, and the like of the Ge crystal layer 106.
By subjecting the Ge crystal layer 106 to annealing with the temperature and the duration being set as above, the defects can be moved within the Ge crystal layer 106 and trapped, for example, by the boundary between the Ge crystal layer 106 and the inhibition layer 104. In this way, the annealing causes the defects that were present within the Ge crystal layer 106 to get together at the boundary. Therefore, the density of the defects within the Ge crystal layer 106 is reduced. As a result, the surface of the Ge crystal layer 106 that is externally exposed through the opening 105 achieves better crystallinity than before the annealing.
This reduces the defects in an epitaxial thin film, thereby improving the performance of the electronic device 100. For example, when the surface of the Ge crystal layer 106 that is externally exposed in the opening 105 is used as a nucleus to grow the seed compound semiconductor crystal 108, the seed compound semiconductor crystal 108 accomplishes enhanced crystallinity. Furthermore, the use of the Ge crystal layer 106 with excellent crystallinity to constitute a semiconductor wafer makes it possible to form a high-quality thin film of such a type that cannot be directly grown on the Si crystal layer 166 because of lattice mismatch.
The Ge crystal layer 106 is locally formed in part of the region between the second compound semiconductor crystal 112 and the Si crystal layer 166, and may have a lattice match or a pseudo lattice match with the second compound semiconductor crystal 112. Thus, the Ge crystal layer 106 achieves a low density of defects.
As used herein, a low density of defects indicates a case where an average number of threading dislocations is 0.1 or smaller within a crystal layer of a prescribed size. Here, a threading dislocation is defined as a defect that penetrates through the Ge crystal layer 106. The case where the average number of threading dislocations is 0.1 is equivalent to a case where testing ten devices having an active layer of approximately 10 μm×10 μm discovers that one of the devices has threading dislocations. The case where the average number of threading dislocations is 0.1 is, in terms of dislocation density, equivalent to a case where the average dislocation density, which is measured by the etch-pit method or horizontal cross-section observation based on a transmission electron microscope (hereinafter, may be referred to as TEM), is approximately 1.0×105 cm−2 or lower.
The plane of the Ge crystal layer 106, the plane facing the seed compound semiconductor crystal 108, may be subjected to surface treatment with a P-containing gas. This can enhance the crystallinity of the film formed on the Ge crystal layer 106. The P-containing gas may be a gas containing PH3 (phosphine).
The Ge crystal layer 106 can be formed, for example, by CVD or MBE (molecular beam epitaxy). The source gas used may be GeH4. The Ge crystal layer 106 may be formed by CVD under the pressure of no less than 0.1 Pa and no more than 100 Pa. This makes the growth rate of the Ge crystal layer 106 less likely to be affected by the area of the opening 105. This results in the more uniform thickness for the Ge crystal layer 106, for example. In this case, a Ge crystal can be prevented from being deposited on the surface of the inhibition layer 104.
The Ge crystal layer 106 may be formed by CVD within an atmosphere that contains a halogen-containing gas as at least part of the source gas. The halogen-containing gas may be a hydrogen chloride gas or chlorine gas. In this manner, a Ge crystal can be prevented from being deposited on the surface of the inhibition layer 104 even when the Ge crystal layer 106 is formed by CVD under the pressure of 100 Pa or higher.
In the present embodiment, the case where the Ge crystal layer 106 is in contact with the surface of the SOI wafer 102 has been explained. However, the positional relationship between the Ge crystal layer 106 and the SOI wafer 102 is not limited to such. For example, any other layers may be disposed between the Ge crystal layer 106 and the SOI wafer 102. Here, one or more layers may be disposed between the Ge crystal layer 106 and the SOI wafer 102.
For example, the Ge crystal layer 106 is formed according to the following procedure. To begin with, a seed crystal is formed at a low temperature. The seed crystal may be SixGe1-x (0≦x<1). The seed crystal may be grown at a temperature of no less than 330° C. and no more than 450° C. After this, the temperature of the SOI wafer 102, on which the seed crystal has been formed, is raised to a prescribed level. Subsequently, the Ge crystal layer 106 may be formed.
The seed compound semiconductor crystal 108 may be grown by using the Ge crystal layer 106 as a nucleus so that the upper portion of the seed compound semiconductor crystal 108 protrudes from the surface of the inhibition layer 104. For example, the seed compound semiconductor crystal 108 is grown within the opening 105 until protruding above the surface of the inhibition layer 104.
The seed compound semiconductor crystal 108 is, for example, a group IV, III-V, or II-VI compound semiconductor that has a lattice match or a pseudo lattice match with the Ge crystal layer 106. More specifically, the seed compound semiconductor crystal 108 may be GaAs, InGaAs, SixGe1-x (0≦x<1). A buffer layer may be formed between the seed compound semiconductor crystal 108 and the Ge crystal layer 106. The buffer layer has a lattice match or a pseudo lattice match with the Ge crystal layer 106. For example, the buffer layer includes a group III-V compound semiconductor layer containing P.
The seed compound semiconductor crystal 108 is an exemplary functional layer. The seed compound semiconductor crystal 108 is formed in contact with the Ge crystal layer 106. In other words, the seed compound semiconductor crystal 108 is grown on the Ge crystal layer 106. For example, the seed compound semiconductor crystal 108 is epitaxially grown.
The seed compound semiconductor crystal 108 has an arithmetic mean deviation of the profile (hereinafter, may be referred to as a Ra value) of 0.02 μm or smaller, preferably 0.01 μm or lower, for example. In this way, the seed compound semiconductor crystal 108 can be used to manufacture high-performance devices. Here, the Ra value is an index representing surface roughness and can be calculated based on JIS B0601-2001. The Ra value can be calculated by turning a roughness curve of a prescribed length at the center line and dividing the area defined by the roughness curve and the center line by the measured length.
The seed compound semiconductor crystal 108 may be grown at the rate of 300 nm/min or lower, preferably 200 nm/min or lower, more preferably 60 nm/min or lower. In this way, the Ra value of the seed compound semiconductor crystal 108 can be controlled 0.02 μm or smaller. On the other hand, the seed compound semiconductor crystal 108 may be grown at the rate of 1 nm/min or higher, preferably 5 nm/min or higher. In this way, the seed compound semiconductor crystal 108 with a high quality is obtained without sacrificing the productivity. For example, the seed compound semiconductor crystal 108 may be grown at the rate of no less than 1 nm/min and no more than 300 nm/min.
In the present embodiment, the case where the seed compound semiconductor crystal 108 is formed on the surface of the Ge crystal layer 106 has been explained. However, the present invention is not limited to such. For example, an intermediate layer may be disposed between the Ge crystal layer 106 and the seed compound semiconductor crystal 108. The intermediate layer may be constituted by a single layer or by a plurality of layers. The intermediate layer may be formed at the temperature of 600° C. or lower, preferably 550° C. or lower. This improves the crystallinity of the seed compound semiconductor crystal 108. On the other hand, the intermediate layer may be formed at the temperature of 400° C. or higher. The intermediate layer may be formed at the temperature of no less than 400° C. and no more than 600° C. This improves the crystallinity of the seed compound semiconductor crystal 108. The intermediate layer is a GaAs layer that is formed at the temperature of 600° C. or lower, preferably 550° C. or lower, for example.
The seed compound semiconductor crystal 108 may be formed according to the following procedure. To begin with, an intermediate layer is formed on the surface of the Ge crystal layer 106. The intermediate layer is grown, for example, at the temperature of 600° C. or lower. After this, the temperature of the SOI wafer 102, on which the intermediate layer has been formed, is raised to a prescribed level. Subsequently, the seed compound semiconductor crystal 108 may be formed.
The first compound semiconductor crystal 110 may be laterally grown along the inhibition layer 104 by using, as the seed plane of the nucleus, a prescribed plane of the seed compound semiconductor crystal 108 that protrudes above the surface of the inhibition layer 104. When the SOI wafer 102 has a plane orientation of (100) and the opening 105 extends in the <001> direction, the seed planes of the seed compound semiconductor crystal 108 include the (110) plane and the plane equivalent to the (110) plane. When the opening 105 extends in the <011> direction, the seed planes of the seed compound semiconductor crystal 108 include the (111)A plane and the plane that is equivalent to the (111)A plane. Since the annealing or the like has improved the crystallinity of the seed compound semiconductor crystal 108, the first compound semiconductor crystal 110 with excellent crystallinity can be formed.
The first compound semiconductor crystal 110 may be a group IV, III-V, or II-VI compound semiconductor that has a lattice match or a pseudo lattice match with the seed compound semiconductor crystal 108. For example, the first compound semiconductor crystal 110 may be GaAs, InGaAs, SixGe1-x (0≦x<1).
The second compound semiconductor crystal 112 is laterally grown along the inhibition layer 104 by using, as a seed plane, a prescribed plane of the first compound semiconductor crystal 110. As mentioned earlier, the second compound semiconductor crystal 112 may be laterally grown in a different direction than that of the first compound semiconductor crystal 110.
The second compound semiconductor crystal 112 may have a lattice match or a pseudo lattice match with the Ge crystal layer 106. Since the second compound semiconductor crystal 112 is grown by using, as a seed plane, a particular plane of the first compound semiconductor crystal 110 with excellent crystallinity, the second compound semiconductor crystal 112 achieves excellent crystallinity. Thus, the second compound semiconductor crystal 112 has a defect-free region including no defects.
The second compound semiconductor crystal 112 may include a group II-VI or III-V compound semiconductor that has a lattice match or a pseudo lattice match with the Ge crystal layer 106. For example, the second compound semiconductor crystal 112 includes a GaAs or InGaAs layer.
The SOI wafer 102 may have an Si1-xGex layer (0<x<1) therein in the portion at which the SOI wafer 102 is in contact with the Ge crystal layer 106, where the Si1-xGex layer is in contact with the boundary between the SOI wafer 102 and the Ge crystal layer 106. In other words, the Ge atoms within the Ge crystal layer 106 may diffuse into the SOT wafer 102 to form a SiGe layer. In this case, the crystallinity of the epitaxial layer formed on the Ge crystal layer 106 can be improved. The average Ge composition x in the Si1-xGex layer can be 60% or higher in the region that is spaced, by a distance of no less than 5 nm and no more than 10 nm, away from the boundary between the SDI wafer 102 and the Ge crystal layer 106. In this case, the crystallinity of the epitaxial layer formed on the Ge crystal layer 106 can be particularly improved.
In the present embodiment, the case where the second compound semiconductor crystal 112 is laterally grown along the inhibition layer 104 by using, as a seed plane, a particular plane of the first compound semiconductor crystal 110 has been explained. Alternatively, however, the seed compound semiconductor crystal 108 and the first compound semiconductor crystal 110 may be integrally formed as a single-piece compound semiconductor crystal. The second compound semiconductor crystal 112 may be laterally grown on the inhibition layer 104 by using, as a seed plane, a particular plane of the single-piece compound semiconductor crystal. The single-piece seed compound semiconductor crystal may be grown by using the Ge crystal layer 106 as a nucleus and protrude above the surface of the inhibition layer 104. In this manner, the inhibition layer 104 is at least partially positioned between the second compound semiconductor crystal 112 and the insulating layer 164 of the SOT wafer 102.
On the defect-free region of the second compound semiconductor crystal 112, an active element having an active region may be formed. The active element is, for example, a MISFET including the gate insulator 114, the gate electrode 116, and the source/drain electrodes 118. The MISFET may be a metal-oxide-semiconductor field-effect transistor (MOSFET). The active element may alternatively be a HEMT.
The gate insulator 114 electrically insulates the gate electrode 116 from the second compound semiconductor crystal 112. The gate insulator 114 is, for example, an AlGaAs film, an AlInGaP film, a silicon oxide film, a silicon nitride film, an aluminum oxide film, a gallium oxide film, a gadolinium oxide film, a hafnium oxide film, a zirconium oxide film, a lanthanum oxide film, and a mixture or a multilayer film of these insulating films.
The gate electrode 116 is an exemplary control electrode. The gate electrode 116 controls the current or voltage between the input and output electrodes such as the source and drain electrodes. The gate electrode 116 may include a metal such as aluminum, copper, gold, silver, platinum, and tungsten, a highly-doped semiconductor such as silicon, tantalum nitride, a metallic silicide or the like.
The source/drain electrodes 118 are exemplary input and output electrodes. The source/drain electrodes 118 are respectively in contact with the source and drain regions. The source/drain electrodes 118 may include a metal such as aluminum, copper, gold, silver, platinum, and tungsten, a highly-doped semiconductor such as silicon, tantalum nitride, a metallic silicide or the like.
Under the source/drain electrodes 118, the source and drain regions are formed. An active layer, which is positioned under the gate electrode 116 and in which a channel region is to be formed between the source region and the drain region, may be the second compound semiconductor crystal 112 itself or a layer formed on the second compound semiconductor crystal 112. A buffer layer may be formed between the second compound semiconductor crystal 112 and the active layer. The active layer or buffer layer may be a GaAs layer, an InGaAs layer, an AlGaAs layer, an InGaP layer, a ZnSe layer or the like.
As shown in
Since the second compound semiconductor crystals 112 are not in contact with each other, no boudaries are formed between adjacent second compound semiconductor crystals 112. Therefore, no defects are generated resulting from such boundaries.
Active elements, which are to be formed on the second compound semiconductor crystals 112, only require excellent crystallinity for their active layers. Thus, the active elements are not adversely affected by the fact that the second compound semiconductor crystals 112 are not in contact with each other.
To increase the driving currents applied to each of the active elements, the active elements are, for example, connected to each other in parallel. In the electronic device shown as an example in
In the present embodiment, the case where the Ge crystal layer 106 is formed by being selectively grown within the opening 105 has been explained. Alternatively, however, the Ge crystal layer 106 may be formed by patterning a Ge film formed on the Si crystal layer 166 based on etching or the like. Furthermore, in the present embodiment, the case where a plurality of Ge crystal layers 106 are formed on a single Si crystal layer 166 has been explained. Alternatively, however, a plurality of Ge crystal layers 106 may be formed on a single Si crystal layer 166 or a plurality of discrete Si crystal layers 166 that are formed using etching or the like. In this way, the individual Ge crystal layers 106 are formed on, for example, island-like Si crystal layers 166. As a result, the peripheral portions of the Ge crystal layers 106 serve as defect traps.
In the present embodiment, the case where the seed crystal layer includes Ge crystal has been explained. The seed crystal layer may include SixGe1-x (0≦x<1). The seed crystal layer may include SixGe1-x with a low content of Si. The seed crystal layer may include GaAs that is formed at the temperature of 500° C. or lower. The seed crystal layer may include a plurality of layers.
In the present embodiment, the case where the Si wafer 162, the insulating layer 164, the Si crystal layer 166, the Ge crystal layer 106, and the compound semiconductor that has a lattice match or a pseudo lattice match with the annealed Ge crystal layer 106 are arranged in the stated order in the substantially perpendicular direction to the main plane 172 of the Si wafer 162 has been explained. However, the positional relations between the respective components are not limited in this regard. For example, the compound semiconductor may be in contact with at least one among the planes of the Ge crystal layer 106, the planes being substantially perpendicular to the main plane 172 of the Si wafer 162 and have a lattice match or a pseudo lattice match with the Ge crystal layer 106. In this case, the Ge crystal layer 106 and the compound semiconductor are arranged adjacent to each other in the substantially parallel direction to the main plane 172 of the Si wafer 162.
As yet another example, in at least part of the Si wafer 162, the Si wafer 162, the insulating layer 164, the Si crystal layer 166, and the inhibition layer 104 are arranged in the stated order in the substantially perpendicular direction to the main plane 172 of the Si wafer 162, and the Si crystal layer 166, the Ge crystal layer 106, and the compound semiconductor may be arranged in the stated order in the substantially parallel direction to the main plane 172. A single Si crystal layer 166 or a plurality of discrete Si crystal layers 166 may be provided on the insulating layer 164 by means of etching or the like. The compound semiconductor has a lattice match or a pseudo lattice match with the annealed Ge crystal layer 106. The Si crystal layer 166, the Ge crystal layer 106, and the compound semiconductor may be provided on the insulating layer 164.
In this example, the inhibition layer 104 may be provided so as to cover a plane of the Si crystal layer 166, the plane being substantially parallel to the main plane 172 of the Si wafer 162. The inhibition layer 104 is formed in a manner to at least partially expose a plane of the Si crystal layer 166, the plane being substantially perpendicular to the main plane 172 of the Si wafer 162. The Ge crystal layer 106 may be formed so as to be in contact with a plane that is not covered with the inhibition layer 104 among the planes of the Si crystal layer 166, the planes being substantially perpendicular to the main plane 172 of the Si wafer 162. The compound semiconductor may be in contact with at least one among the planes of the Ge crystal layer 106, the planes being substantially perpendicular to the main plane 172 of the Si wafer 162 and have a lattice match or a pseudo lattice match with the Ge crystal layer 106. The compound semiconductor may be in contact with the plane of the Ge crystal layer 106, the plane being substantially parallel to the main plane 172 of the Si wafer 162 and have a lattice match or a pseudo lattice match with the Ge crystal layer 106.
In the present embodiment, the case where the inhibition layer 104 is formed on the Si crystal layer 166, and the Ge crystal layer 106 is formed within the opening 105 in the inhibition layer 104 has been explained. However, the present invention is not limited in this regard. After the Ge crystal layer 106 has been formed, the inhibition layer 104 may be formed in a region in which the Ge crystal layer 106 is not formed. For example, the inhibition layer 104 of the electronic device 100 may be formed by thermally oxidizing the Si crystal layer 166 while the annealed Ge crystal layer 106 is used as a mask. The inhibition layer 104 is formed so as to surround the Ge crystal layer 106.
Furthermore, the electronic device 100 may include a compound semiconductor that has a lattice match or a pseudo lattice match with the annealed Ge crystal layer 106. The inhibition layer 104 may be formed by thermal oxidization before the compound semiconductor is grown on the Ge crystal layer 106.
After this, a prescribed plane of the seed compound semiconductor crystal 108 is used as a seed plane to form the first compound semiconductor crystal 110. The cross-section observed at this stage is similar to the cross-section shown in
For example, the lateral growth preferably takes place at low temperatures to facilitate the lateral growth on the (001) plane. Specifically speaking, the growth may be controlled to take place at the temperature of 700° C. or lower, preferably at the temperature of 650° C. or lower. For example, the lateral growth preferably takes place with the partial pressure of AsH3 being set high when taking place in the <110> direction. More particularly, the lateral growth is preferably controlled to take place with the partial pressure of AsH3 being set at 1×10−3 atom or higher. In this manner, the growth rate in the <110> direction can be controlled to be higher than the growth rate in the <−110> direction.
For example, the Ge crystal layer 106 is formed on the Si crystal layer 166 of the SOI wafer 102 by forming a crystalline Ge film on the SOI wafer 102 and then removing the Ge film except for its partial region based on etching. The etching can be performed, for example, by photolithography. The Ge crystal layer 106 may have a maximum width of 5 μm or smaller, preferably 2 μm or smaller. As used herein, “a width” is defined as a length in the substantially parallel direction to one of the main planes of the SOI wafer 102.
As shown in
The position of the defect trap 120 is controlled, for example, by forming the opening 105 at a prescribed position. Here, the prescribed position is appropriately designed depending on the purpose of the electronic device 200. There may be a plurality of openings 105. The openings 105 may be arranged at equal intervals. The openings 105 may be formed according to some rules, for example, periodically. In each of the openings 105, the seed compound semiconductor crystal 108 is formed.
The defect centers may be formed by physically damaging the seed plane or the inhibition layer 104. The methods to physically damage the seed plane or the inhibition layer 104 include, for example, mechanical scratching, friction, and ion implantation. Here, the prescribed interval is appropriately designed depending on the purpose of the electronic device 300. There may be a plurality of defect centers. The defect centers may be arranged at equal intervals. The defect centers may be formed according to some rules, for example, periodically.
The defect traps 120 and 130 may be formed during the crystal growth step for the second compound semiconductor crystal 112. If the defect traps 120 and 130 are formed, the defects present within the second compound semiconductor crystal 112 can gather to the defect traps 120 and 130. This can reduce stress and other problems in the region of the second compound semiconductor crystal 112 that excludes the defect traps 120 and 130 and can thus improve the crystallinity in the region. In this manner, defects can be reduced in the region of the second compound semiconductor crystal 112 in which an electronic device is to be formed.
When a compound semiconductor is laterally grown on the (100) plane of the SOI wafer 102, the growth takes place more easily in the <011> direction of a silicon wafer than in the <0-11> direction of the SOI wafer 102. When the compound semiconductor is grown in the <0-11> direction of the SOI wafer 102, the (111)B plane of the compound semiconductor appears at the end plane of the laterally grown compound semiconductor. This (111)B plane is stable and thus likely to be flat. Accordingly, a gate insulator, a source electrode, a gate electrode, and a drain electrode are formed to manufacture an electronic device on the (111)B plane of the compound semiconductor.
On the other hand, when the compound semiconductor is laterally grown in the <011> direction of the SOI wafer 102, the (111)B plane of the compound semiconductor inversely appears at the end plane of the laterally-grown compound semiconductor. In this case, a large (100) plane can be obtained on the upper side. Thus, an electronic device can be formed on the (100) plane. In addition, the compound semiconductor can be also laterally grown in either of the <010> and <001> directions of the SOI wafer 102 with the partial pressure of the arsine being set high. When the compound semiconductor is grown in either of these directions, the (110) or (101) plane of the compound semiconductor is likely to appear at the end plane of the laterally grown compound semiconductor. It is also possible to form a gate insulator, a source electrode, a gate electrode, and a drain electrode to manufacture an electronic device on the (110) or (101) plane of the compound semiconductor.
The buffer layer 402 has a lattice match or a pseudo lattice match with the Ge crystal layer 106. The buffer layer 402 is formed between the Ge crystal layer 106 and the seed compound semiconductor crystal 108. The buffer layer 402 may be a group III-V compound semiconductor containing P. The buffer layer 402 may be an InGaP layer. The InGaP layer is, for example, formed by epitaxial growth.
The InGaP layer is, for example, formed by MOCVD or MBE that uses organic metals as the source. These growth techniques use, as the source gas, trimethyl gallium (TM-Ga), trimethyl indium (TM-In), PH3 (phosphine), for example. When the InGaP layer is epitaxially grown, the crystalline thin film is formed at the temperature of 650° C., for example. The presence of the buffer layer 402 further improves the crystallinity of the seed compound semiconductor crystal 108.
In the case of PH3 treatment, the temperature is preferably set no less than 500° C. and no more than 900° C., for example. This temperature range is preferable since no effects are produced in the case of lower than 500° C. and the Ge crystal layer 106 is modified in the case of higher than 900° C. A more preferable temperature range may be, for example, no less than 600° C. and no more than 800° C. During the exposure, PH3 may be activated by plasmas or the like.
The buffer layer 402 may be a single layer or a plurality of layers. The buffer layer 402 may be formed at the temperature of 600° C. or lower, preferably 550° C. or lower. This improves the crystallinity of the seed compound semiconductor crystal 108. The buffer layer 402 may be a GaAs layer formed at the temperature of 600° C. or lower, preferably 550° C. or lower. The buffer layer 402 may be formed at the temperature of 400° C. or higher. In this case, the plane of the Ge crystal layer 106, the plane facing the buffer layer 402, may be subjected to surface treatment with a gaseous P compound.
The source/drain electrode 502 is an exemplary first input/output electrode. The source/drain electrode 118 is an exemplary second input/output electrode. As shown in
By forming the source/drain electrode 502 so as to also cover the lateral plane of the second compound semiconductor crystal 112, the input/output electrode can be positioned so as to intersect with the extended line in the direction in which carriers move in the second compound semiconductor crystal 112 or the active layer formed thereon (may sometimes be referred to as the carrier movement layer). This facilitates the movement of the carriers, thereby improving the performance of the electronic device 500.
The region of the second compound semiconductor crystal 112 that is positioned above the opening 105 has been removed, for example, by etching. The etching externally exposes a lateral plane of the second compound semiconductor crystal 112. As shown in
The source/drain electrode 602 is connected to the Si crystal layer 166 via the Ge crystal layer 106 or the seed compound semiconductor crystal 108 in the opening 105 externally exposed by the etching. This enables the potential of one of the input/output terminals of the MISFET to be maintained at the wafer potential, thereby reducing noise.
The lower gate electrode 704 opposes the gate electrode 116 with the second compound semiconductor crystal 112 being sandwiched therebetween. The lower gate electrode 704 may be formed in a groove formed in the surface of the inhibition layer 104. The lower gate insulator 702 is formed between the lower gate electrode 704 and the second compound semiconductor crystal 112.
By disposing the gate electrode 116 and the lower gate electrode 704 as described above in the electronic device 700, a double gate structure can be easily realized. This can accomplish better gate control and thus improve the switching and other capabilities of the electronic device 700.
The SOI wafer 802 is equivalent to the SOI wafer 102. In other words, the Ge crystal layers 106 are arranged at equal intervals on the Si crystal layer 166.
In the semiconductor wafer 801 of the present embodiment, a heterojunction bipolar transistor (hereinafter, may be referred to as HBT) is formed as an electronic element in the opening 806 shown in
In at least a partial region of the SOI wafer 802, a Si wafer 862, an insulating layer 864, and a Si crystal layer 866 are arranged in the stated order. The Si wafer 862, the insulating layer 864, and the Si crystal layer 866 are equivalent to the Si wafer 162, the insulating layer 164, and the Si crystal layer 166 of the electronic device 100. The Si wafer 862 has a main plane 872. The main plane 872 is equivalent to the main plane 172 of the Si wafer 162.
The inhibition layer 804 is formed on the Si crystal layer 866 to inhibit crystal growth of the compound semiconductor functional layer 824. The inhibition layer 804 inhibits epitaxial growth of the compound semiconductor functional layer 824. The inhibition layer 804 is equivalent to the inhibition layer 104.
The inhibition layer 804 is provided to cover part of the Si crystal layer 866. In the inhibition layer 804, the opening 806 is formed that penetrates through the inhibition layer 804 to reach the Si crystal layer 866. The surface of the inhibition layer 804 may be shaped as a square, and the opening 806 may be positioned at the center of the surface of the inhibition layer 804. The inhibition layer 804 may be in contact with the Si crystal layer 866.
The Ge crystal layer 820 has the same configuration as the Ge crystal layer 106. For example, the Ge crystal layer 820 is grown within the opening 806 in the inhibition layer 804. The Ge crystal layer 820 is selectively grown within the opening 806.
The inhibition layer 804 inhibits epitaxial growth on the surface of the inhibition layer 804. Thus, the Ge crystal layer 820 is not formed on the surface of the inhibition layer 804. On the other hand, the Ge crystal layer 820 is formed on the Si crystal layer 866 within the opening 806 since the region of the Si crystal layer 866 that is externally exposed through the opening 806 is not covered by the inhibition layer 804. The Ge crystal layer 820 may be in contact with the Si crystal layer 866 or formed on the Si crystal layer 866 with an intermediate layer disposed therebetween.
The buffer layer 822 has a lattice match or a pseudo lattice match with the Ge crystal layer 820. The buffer layer 822 has the same configuration as the buffer layer 402. The buffer layer 822 is sandwiched between the Ge crystal layer 820 and the compound semiconductor functional layer 824. The buffer layer 822 may be a group III-V compound semiconductor layer containing P. For example, the buffer layer 822 is an InGaP layer. The InGaP layer is epitaxially grown, for example.
When the InGaP layer is epitaxially grown in contact with the Si crystal layer 866, the InGaP layer is not formed on the surface of the inhibition layer 804 and selectively grown on the surface of the Ge crystal layer 820. As another example, the buffer layer 822 may be a GaAs layer that is grown on the Si crystal layer 866 at the temperature of 500° C. or lower. The semiconductor wafer 801 may be realized without the buffer layer 822. In this case, the plane of the Ge crystal layer 820, the plane facing the compound semiconductor functional layer 824, may be subjected to surface treatment with a P-containing gas.
The compound semiconductor functional layer 824 has a lattice match or a pseudo lattice match with the Ge crystal layer 820. The compound semiconductor functional layer 824 is used, for example, for manufacturing a HBT. The HBT is shown as an exemplary electronic element. The compound semiconductor functional layer 824 may be in contact with the Ge crystal layer 820. In other words, the compound semiconductor functional layer 824 may be in contact with the Ge crystal layer 820 or formed on the Ge crystal layer 820 with the buffer layer 822 disposed therebetween. The compound semiconductor functional layer 824 may be formed by crystal growth. For example, the compound semiconductor functional layer 824 is formed by epitaxial growth.
The compound semiconductor functional layer 824 may be a group 111-V or II-VI compound layer that has a lattice match or a pseudo lattice match with the Ge crystal layer 820. The compound semiconductor functional layer 824 may be a group III-V compound layer that has a lattice match or a pseudo lattice match with the Ge crystal layer 820, and contain at least one among Al, Ga, and In as the group III element and at least one among N, P, As, and Sb as the group V element. For example, the compound semiconductor functional layer 824 is a GaAs or InGaAs layer.
In the compound semiconductor functional layer 824, a HBT is formed as an electronic element. Here, the present embodiment takes an HBT as an example of the electronic element formed in the compound semiconductor functional layer 824. The electronic element, however, is not limited to an HBT, but may alternatively be a light emitting diode, a high electron mobility transistor (hereinafter, may be referred to as HEMT), a solar cell, or a thin film sensor.
On the surface of the compound semiconductor functional layer 824, a collector mesa, an emitter mesa, and a base mesa for the HBT are formed. The collector electrode 808, the emitter electrode 810, and the base electrode 812 connected to contact holes are formed on the surfaces of the collector mesa, the emitter mesa, and the base mesa. The compound semiconductor functional layer 824 includes the collector, emitter, and base layers of the HBT. Specifically speaking, the collector layer is formed on the buffer layer 822, the emitter layer is formed between the buffer layer 822 and the collector layer, and the base layer is formed between the buffer layer 822 and the emitter layer.
The collector layer may be a multilayer film obtained by stacking an n+GaAs layer having a carrier concentration of 3.0×1018 cm−3 and the thickness of 500 nm and an n−GaAs layer having a carrier concentration of 1.0×1016 cm−3 and the thickness of 500 nm in the stated order. The emitter layer may be a multilayer film obtained by stacking an n−InGaP layer having a carrier concentration of 3.0×1017 cm−3 and the thickness of 30 nm, an n+GaAs layer having a carrier concentration of 3.0×1018 cm−3 and the thickness of 100 nm, and an n+InGaAs layer having a carrier concentration of 1.0×1019 cm−3 and the thickness of 100 nm in the stated order. The base layer may be a p-GaAs layer having a carrier concentration of 5.0×1019 cm−3 and the thickness of 50 nm. It should be noted that the above-mentioned carrier concentration and thickness values are designed values.
A MISFET 880 may be formed in at least part of the region of the Si layer in which the compound semiconductor functional layer 824 is not formed. As shown in
The Si layer other than the compound semiconductor functional layer 824 may be the Si wafer 862 or the Si crystal layer 866. The MISFET 880 may be formed in a region of the Si crystal layer 866, the region being not covered by the Ge crystal layer 820.
The Si wafer 862 may be a single crystal Si wafer. In this case, the MISFET 880 may be formed in a region of the single crystal Si wafer that is covered neither by the Ge crystal layer 820 nor by the insulating layer 864. On the Si wafer 862 or the Si crystal layer 866, there may be not only electronic elements such as active and functional elements that are formed by processing the Si layer but also at least one among interconnections formed on the Si layer, interconnections including Si, electronic circuits formed by combining these interconnections, and micro electro mechanical systems (MEMS).
In the present embodiment, the case where the seed crystal layer includes a Ge crystal formed by crystal growth has been explained. The present invention, however, is not limited in this regard. As in the electronic device 100, the seed crystal layer may be made of SixGe1-x (0≦x<1). The seed crystal layer may be made of SixGe1-x with a low Si content. The seed crystal layer may include GaAs formed at the temperature of 500° C. or lower.
The Ge crystal layer 1120 is equivalent to the Ge crystal layer 106 of the electronic device 100 or the Ge crystal layer 820 of the semiconductor wafer 801. The Ge crystal layer 106 or 820 is selectively grown within the opening 105 or 806. The Ge crystal layer 1120 is different from the Ge crystal layers 106 and 820. Specifically speaking, a single Ge crystal layer 1120 or a plurality of discrete Ge crystal layers 1120 are formed by etching, mechanically scratching, applying friction to, or performing ion implantation on a Ge film that has been formed on the SOI wafer 1102. The single island-like Ge crystal layer 1120 or the plurality of discrete island-like Ge crystal layers 1120 is an example of a single Ge crystal layer or a plurality of discrete Ge crystal layers. The crystal boundaries of the island-like Ge crystal layers serve as defect traps. Thus, annealing the Ge crystal layers 1120 can reduce the density of the defects within the Ge crystal layers 1120.
The Ge crystal layer 1120 may be formed like an isolated island on the Si crystal layer 1166. The Ge crystal layer 1120 may be grown on the Si crystal layer 1166.
The InGaP layer 1122 is an exemplary buffer layer. The InGaP layer 1122 has the same configuration as the buffer layer 822. The compound semiconductor functional layer 1124 has the same configuration as the compound semiconductor functional layer 824.
On the surface of the compound semiconductor functional layer 1124, a collector mesa, an emitter mesa, and a base mesa for the HBT are formed. A collector electrode 1108, an emitter electrode 1110, and a base electrode 1112 are formed on the surfaces of the collector mesa, the emitter mesa, and the base mesa via contact holes. The compound semiconductor functional layer 1124 includes the collector, emitter, and base layers of the HBT.
In the present embodiment, the case where the seed crystal layer includes a Ge crystal has been explained. As in the electronic device 100 and the semiconductor wafer 801, however, the seed crystal layer may include SixGe1-x (0≦x<1). The seed crystal layer may be made of SixGe1-x with a low Si content. The seed crystal layer may include a GaAs or an InGaAs layer formed at the temperature of 500° C. or lower. In the present embodiment, an InGaP layer 1123 and an accompanying layer 1125 are additionally formed during the manufacturing process.
As shown in
As shown in
The above-described procedure can reduce the defects that may be generated by the wafer materials in a subsequently-formed epitaxial thin film, for example. As a result, the electronic element formed in the compound semiconductor functional layer 1124 achieves improved performance.
As shown in
The InGaP layers 1122 and 1123 are, for example, epitaxially grown by MOCVD or MBE that uses organic metals as the source. In this case, trimethyl gallium (TM-Ga), trimethyl indium (TM-In), PH3 (phosphine), can be used as the source gas. When an InGaP layer is epitaxially grown, the crystal thin film is formed under a high-temperature atmosphere at the temperature of 650° C., for example.
As shown in
The compound semiconductor functional layer 1124 may be a GaAs layer or GaAs-based multilayer film including InGaAs and the like. The GaAs layer or GaAs-based multilayer film may be epitaxially grown, for example, by MOCVD or MBE using organic metals as the source. Here, trimethyl gallium (TM-Ga), AsH3 (arsine) and other gasses can be used as the source gas. The growth take places, for example, at the temperature from 600° C. to 650° C. Subsequently, an electronic element such as an HBT is formed in the compound semiconductor functional layer 1124, as a result of which the semiconductor wafer 1101 can be obtained.
In the present embodiment, the case where the annealing is carried out after the Ge crystal layer 1120 has been formed has been explained. Alternatively, however, the annealing may be carried out after the InGaP layer 1122 has been formed. In other words, after the Ge crystal layer 1120 has been formed, the InGaP layers 1122 and 1123 may be subsequently formed before the annealing is performed. After the InGaP layers 1122 and 1123 have been formed, all of the Ge crystal layer 1120 and the InGaP layers 1122 and 1123 may be subjected to annealing.
For example, a GaAs film is grown on the surface of the SOI wafer 1102, which has been exposed to PH3. After this, the GaAs film is subjected to etching by photolithography, so that the isolated island-like compound semiconductor functional layers 1124 are formed. After the surface of the Si wafer has been subjected to surface treatment with a gaseous P compound, a GaAs layer may be formed as a seed crystal layer at the temperature of 500° C. or lower. This achieves improved crystallinity of the compound semiconductor functional layer 1124.
In accordance with the procedure shown in
The Si wafer 162 of the SOI wafer 102 was a single crystal Si wafer. SiO2 was deposited by CVD to form the inhibition layer 104. After this, the openings 105 were formed in the inhibition layer 104 by photolithography. Here, the openings 105 were controlled to have an aspect ratio of 1. The Ge crystal layers 106 were formed by CVD using GeH4 as the source gas. The maximum width of the Ge crystal layers 106 was set to 2 μm in the substantially parallel direction to the surface of the SOI wafer 102. After the Ge crystal layers 106 were formed, two-phase annealing was carried out that includes high-temperature annealing at the temperature of 800° C. for 10 minutes and low-temperature annealing at the temperature of 680° C. for 10 minutes. The above-described two-phase annealing was performed ten times. In the above-described manner, the semiconductor wafer was fabricated.
On the Ge crystal layers 106 of the semiconductor wafer, GaAs crystals were formed as the seed compound semiconductor crystals 108, the first compound semiconductor crystals 110 and the second compound semiconductor crystals 112. The GaAs crystals were grown by MOCVD at the temperature of 650° C. using TM-Ga and AsH3 as the source gases. The second compound semiconductor crystal 112 was grown with the partial pressure of AsH3 being set to 1×10−3 atm. On the second compound semiconductor crystal 112, the gate insulator 114 made of highly resistant AlGaAs, the gate electrode 116 made of Pt, and the source/drain electrodes 118 made of W were formed. Thus, the electronic device 100 was fabricated.
The semiconductor wafer with the Ge crystal layers 106 having been formed was examined as to whether defects were generated on the surfaces of the Ge crystal layers 106. The examination utilized the etch-pit method. The examination discovered no defects on the surfaces of the Ge crystal layers 106. Furthermore, ten electronic devices 100 were examined as to whether threading defects were generated. The examination was performed by in-plane cross-section observation with a TEM. The examination discovered that none of the electronic devices 100 had threading defects.
According to the present embodiment, the Ge crystal layers 106 were formed within the openings 105 having an aspect ratio of √3/3 or higher. Therefore, the Ge crystal layers 106 had excellent crystallinity at the surfaces thereof at the time of being deposited. Furthermore, the present embodiment subjected the Ge crystal layers 106 to annealing, thereby further improving the crystallinity of the Ge crystal layers 106. Since the Ge crystal layers 106 achieved improved crystallinity, enhanced crystallinity was also realized for the seed compound semiconductor crystal 108, which was grown by using the Ge crystal layer 106 as a nucleus, for the first compound semiconductor crystal 110, which was grown by using a specific plane of the seed compound semiconductor crystal 108 as a seed plane, and for the second compound semiconductor crystal 112, which was grown by using a specific plane of the first compound semiconductor crystal 110 as a seed plane.
Thus, enhanced crystallinity was realized for the active layer of the electronic device 100, which was formed on the second compound semiconductor crystal 112. The electronic device 100 thus accomplished improved performance despite being formed on the low-cost SOI wafer 102. According to the electronic device 100 relating to the present embodiment, the electronic element was formed in the second compound semiconductor crystal 112 formed on the SOI wafer 102. Therefore, the stray capacitance was decreased and the operating speed was resultantly increased for the electronic device 100. Furthermore, the leakage currents to the Si wafer 162 could be reduced.
The semiconductor wafer 801 with 2500 regions 803 was fabricated in the following manner. The Si wafer 862 of the SOI wafer 802 was a single crystal Si wafer. The inhibition layers 804 of silicon oxide were formed by CVD and the openings 806 were subsequently formed by photolithography. The openings 806 were controlled to have an aspect ratio of 1. The openings 806 were shaped into a square with a side of 100 μm. Adjacent openings 806 were arranged away from each other with a distance of 500 μm therebetween. Within the openings 806, the Ge crystal layers 820 were formed. The Ge crystal layers 820 were formed by MOCVD using GeH4 as the source gas. The maximum width of the Ge crystal layers 820 was set to 2 μm in the substantially parallel direction to the surface of the SOI wafer 802. After the Ge crystal layers 820 were formed, two-phase annealing was carried out that includes high-temperature annealing at the temperature of 800° C. for 2 minutes and low-temperature annealing at the temperature of 680° C. for 2 minutes. The above-described two-phase annealing was performed ten times.
The semiconductor wafer 801 with the Ge crystal layers 820 having been formed was examined as to whether defects were generated on the surfaces of the Ge crystal layers 820. The examination utilized the etch-pit method. The examination discovered no defects on the surfaces of the Ge crystal layers. According to the above-described procedure, the Ge crystal layer 820 was selectively grown within the opening 806 defined by the inhibition layer 804, and the Ge crystal layer 820 was subjected to the two-phase annealing multiple times. In this manner, the Ge crystal layer 820 accomplished improved crystallinity. Furthermore, forming an InGaP layer as the buffer layer 822 contributed to fabricate the semiconductor wafer 801 including a GaAs layer as the compound semiconductor functional layer 824 with excellent crystallinity.
After this, the semiconductor wafer 801 fabricated in the above-described manner was utilized to fabricate an electronic device. The electronic device was fabricated in the following manner. The buffer layer 822 of InGaP was formed on the Ge crystal layer 820 in each region 803. The buffer layer 822 was grown by MOCVD at the temperature of 650° C. using TM-Ga, TM-In and PH3 as the source gases.
On the buffer layer 822, an n+GaAs layer having a carrier concentration of 3.0×1018 cm−3 and the thickness of 500 nm and an n−GaAs layer having a carrier concentration of 2.0×1016 cm−3 and the thickness of 500 nm are formed in the stated order to form the collector layer of the HBT. On the collector layer, a p-GaAs layer having a carrier concentration of 5.0×1019 cm−3 and the thickness of 50 nm was formed to form the base layer of the HBT. On the base layer, an n−InGaP layer having a carrier concentration of 3.0×1017 cm−3 and the thickness of 30 nm, an n+GaAs layer having a carrier concentration of 3.0×1018 cm−3 and the thickness of 100 μm, and an n+InGaAs layer having a carrier concentration of 1.0×1019 cm−3 and the thickness of 100 nm were formed in the stated order to form the emitter layer of the HBT. It should be noted that the above-mentioned carrier concentration and thickness values are designed values.
In the above-described manner, the compound semiconductor functional layer 824 including the base, emitter, and collector layers was formed. The GaAs layers of the base, emitter, and collector layers were grown by MOCVD at the temperature of 650° C. using TM-Ga and AsH3 as the source gases. After this, etching was performed to form a base layer electrode interconnection, an emitter layer electrode interconnection, and a collector layer electrode interconnection. On the surface of the compound semiconductor functional layer 824, the collector electrode 808, the emitter electrode 810, and the base electrode 812 were formed, as a result of which the HBT was fabricated. On the emitter and collector layers, an AuGeNi layer was formed by vacuum vapor deposition. On the base layer, an AuZn layer was formed by vacuum vapor deposition. After formed, the AuGeNi and AuZn layers were thermally treated under a hydrogen atmosphere at the temperature of 420° C. for 10 minutes to form the electrodes. The electrodes were electrically connected to the above-described driving circuits, so that the electronic device was fabricated.
In the above-described manner, a small-sized and low-power-consumption electronic device was accomplished. Furthermore, examination with a secondary electron microscope (hereinafter, may be referred to as SEM) did not find surface roughness on the order of μm on the surface of the compound semiconductor functional layer 824.
The semiconductor wafer 801 was fabricated that has a GaAs buffer layer formed at the temperature of 500° C. or lower between the Si crystal layer 866 and the Ge crystal layer 820. This semiconductor wafer 801 was fabricated in the same manner as in Exemplary Embodiment 2 except that the buffer layer was formed between the Si crystal layer 866 and the Ge crystal layer 820. The GaAs buffer layer was grown by MOCVD at the temperature of 450° C. using TM-Ga and AsH3 as the source gases. This configuration enables the compound semiconductor functional layer 824 to have improved crystallinity.
The semiconductor wafer 801 was fabricated that has the PH3 gas-treated surface of the Ge crystal layer 820. This semiconductor wafer 801 was fabricated in the same manner as in Exemplary Embodiment 2 except that the InGaP buffer layer 822 was omitted and that the compound semiconductor functional layer 824 was formed after the plane of the Ge crystal layer 820, the plane facing the compound semiconductor functional layer 824, was treated with PH3 gas. In this manner, the compound semiconductor functional layer 824 achieved improved crystallinity.
The semiconductor wafer 1101 was fabricated in accordance with the procedure shown in
The semiconductor wafer 1101 with the Ge crystal layers 1120 having been formed was examined as to whether defects were generated on the surfaces of the Ge crystal layers 1120. The examination utilized the etch-pit method. The examination discovered no defects on the surfaces of the Ge crystal layers 1120.
After this, HBTs were fabricated on the Ge crystal layers 1120 to fabricate electronic devices in the same manner as in Exemplary Embodiment 2. In this way, small-sized and low-power-consumption electronic devices were realized. Furthermore, examination with a SEM did not find surface roughness on the order of μm on the surface of the compound semiconductor functional layer 1124.
The semiconductor wafer 1101 with the Ge crystal layers 1120 was fabricated in the same manner as in Exemplary Embodiment 5 except that high-temperature annealing was performed at the temperature of 800° C. for 20 minutes after the Ge crystal layers 1120 were formed. This semiconductor wafer 1101 was examined as to whether defects were generated on the surfaces of the Ge crystal layers 1120. The examination utilized the etch-pit method. The examination discovered no defects on the surfaces of the Ge crystal layers 1120.
After this, HBTs were fabricated on the Ge crystal layers 1120 to fabricate electronic devices in the same manner as in Exemplary Embodiment 2. In this way, small-sized and low-power-consumption electronic devices were realized. Furthermore, examination with a SEM did not find surface roughness on the order of μm on the surface of the compound semiconductor functional layer 1124.
After the Ge crystal layers 1120 were formed, two-phase annealing was carried out that includes high-temperature annealing at the temperature of 900° C. for 10 minutes and low-temperature annealing at the temperature of 780° C. for 10 minutes. The semiconductor wafer 1101 with the Ge crystal layers 1120 was fabricated in the same manner as in Exemplary Embodiment 5 except that the above-mentioned two-phase annealing was performed ten times. This semiconductor wafer 1101 was examined as to whether defects were generated on the surfaces of the Ge crystal layers 1120. The examination utilized the etch-pit method. The examination discovered no defects on the surfaces of the Ge crystal layers 1120.
After this, HBTs were fabricated on the Ge crystal layers 1120 to fabricate electronic devices in the same manner as in Exemplary Embodiment 2. In this way, small-sized and low-power-consumption electronic devices were realized. Furthermore, examination with a SEM did not find surface roughness on the order of μm on the surface of the compound semiconductor functional layer 1124.
Here, the Ge crystal layer 2106 was formed in the following manner. To begin with, the inhibition layer 2104 of SiO2 was formed on the surface of the Si wafer 2102 by thermal oxidization, and a covering region and an opening were defined in the inhibition layer 2104. The outer periphery of the inhibition layer 2104 is equivalent to the outer periphery of the covering region. The Si wafer 2102 was a commercially available single crystal Si wafer. The covering region was shaped as a square with a side of 400 μm in plan view. After this, the Ge crystal layer 2106 was selectively grown by CVD within the opening.
As seen from
The semiconductor wafer was fabricated that includes the Si wafer 2102, the inhibition layer 2104, the Ge crystal layer 2106, and the compound semiconductor 2108, which serves as a device forming layer. It was examined how the rate at which a crystal is grown within the opening 105 formed in the inhibition layer 2104 is related to the size of the covering region and the size of the opening 105. The thickness of the compound semiconductor 2108 that was grown within a prescribed duration was measured while varying the planar shape of the covering region and the bottom shape of the opening 105 defined in the inhibition layer 2104.
To begin with, the covering region and the opening 105 were formed on the surface of the Si wafer 2102 in the following manner. The Si wafer 2102 was, for example, a commercially available single crystal Si wafer. For example, a SiO2 layer was formed by thermal oxidization on the surface of the Si wafer 2102 as an example of the inhibition layer 2104.
The SiO2 layer was etched into SiO2 layers of a prescribed size. Here, three or more SiO2 layers of the prescribed size were formed. The SiO2 layers of the prescribed size were shaped as a square of the same size in plan view. Furthermore, the opening 105 of a prescribed size was formed by etching at the center of each square-shaped SiO2 layer. Here, the center of the opening 105 was controlled to coincide with the center of the square-shaped SiO2 layer. Here, one opening 105 was formed in each one of the square-shaped SiO2 layers. The length of the side of the square-shaped SiO2 layer may be herein referred to as the length of the side of the covering region.
After this, the Ge crystal layer 2106 was selectively grown by MOCVD within the opening 105. GeH4 was used as the source gas. The flow rate of the source gas and the deposition time were respectively set at prescribed values. Subsequently, a GaAs crystal was formed by MOCVD as an example of the compound semiconductor 2108, The GaAs crystal was epitaxially grown on the surface of the Ge crystal layer 2106 within the opening 105 at the temperature of 620° C. and under the pressure of 8 MPa. Trimethyl gallium and arsine were used as the source gases. The flow rates of the source gases and the deposition time were respectively set at prescribed values.
After the compound semiconductor 2108 was formed, the thickness of the compound semiconductor 2108 was measured. The thickness of the compound semiconductor 2108 was calculated in such a manner that a stylus profilometer (Surface Profiler P-10 available from KLA Tencor, Inc.) was used to measure the thickness of the compound semiconductor 2108 at three locations and the resulting three thickness values were averaged. Here, the standard deviation of the thickness values measured at the three locations was also calculated. Alternatively, the thickness may be calculated in such a manner that the thickness of the compound semiconductor 2108 was directly measured at three locations by cross-sectional observation with a transmission or scanning electron microscope and the resulting three thickness values are averaged,
In according with the above-described procedure, the thickness of the compound semiconductor 2108 was measured while the bottom shape of the opening 105 was varied and the length of the side of the covering region was varied between 50 μm, 100 μm, 200 μm, 300 μm, 400 μm, and 500 μm. The bottom shape of the opening 105 was varied between a square with a side of 10 μm, a square with a side of 20 μm, and a rectangle with a short side of 30 μm and a long side of 40 μm.
When the length of the side of the covering region is 500 μm, the plurality of square-shaped SiO2 layers are integrally formed. In this case, the covering regions with a side of 500 μm are not actually arranged at an interval of 500 μm, but this case is referred, for the sake of simplicity, to as the case where the length of the side of the covering region is set at 500 μm. In addition, the distance between two adjacent covering regions is referred to as 0 μm for the sake of simplicity.
The results of the experiments performed in Exemplary Embodiment 9 are shown in
In
The data values shown in
Semiconductor wafers were fabricated in the same manner as in Exemplary Embodiment 9 while the length of the side of the covering region is set at 200 μm, 500 μm, 700 μm, 1000 μm, 1500 μm, 2000 μm, 3000 μm, and 4250 μm, and the thickness of the compound semiconductor 2108 grown within the opening 105 was measured. In Exemplary Embodiment 10, a plurality of SiO2 layers of the same size were arranged on the Si wafer 2102. Furthermore, the SiO2 layers were spaced away from each other. The shape of the bottom of the opening 105 was varied between three options including a square with a side of 10 μm, a square with a side of 20 μm, and a rectangle with a short side of 30 μm and a long side of 40 μm as in Exemplary Embodiment 9. The Ge crystal layer 2106 and the compound semiconductor 2108 were grown under the same conditions as in Exemplary Embodiment 9.
The thickness of the compound semiconductor 2108 grown within the opening 105 was measured when the same conditions were employed as in Exemplary Embodiment 10 except that the supply of trimethyl gallium was reduced to half and the growth rate of the compound semiconductor 2108 was reduced to approximately half. In Exemplary Embodiment 11, experiments were performed while the length of the side of the covering region was set at 200 μm, 500 μm, 1000 μm, 2000 μm, 3000 μm, or 4250 μm, and the bottom of the opening 105 was shaped as a square of 10 μm.
The results of the experiments performed in Exemplary Embodiments 10 and 11 are shown in
In
Table 1 shows the growth rate [Å/min] of the compound semiconductor 2108 and the Ra value [μm] for the experiments performed in Exemplary Embodiments 10 and 11. It should be noted here that the thickness of the compound semiconductor 2108 was measured by means of a stylus profilometer. The Ra value was calculated based on observation with a laser microscope apparatus. Table 1 shows that the surface roughness is improved as the growth rate of the compound semiconductor 2108 is decreased. Table 1 also shows that the Ra value is 0.02 μm or less when the growth rate of the compound semiconductor 2108 is 300 nm/min or less.
In accordance with the same procedure as in Exemplary Embodiment 9, the semiconductor wafer was fabricated that includes the Si wafer 2102, the inhibition layer 2104, the Ge crystal layer 2106, and the compound semiconductor 2108, which is a GaAs crystal, for example. In the present exemplary embodiment, the surface of the Si wafer 2102 on which the inhibition layer 2104 was formed was the (100) plane.
On the other hand, no such planes appear at the lower left and upper right corners of the GaAs crystal in the drawing. For example, the (111) plane is expected to appear at the lower left corner in the drawing, but does not. This is probably because the lower left corner, in the drawing, is between the (110) and (101) planes that are more stable than the (111) plane.
In accordance with the same procedure as in Exemplary Embodiment 9, the semiconductor wafer was fabricated that includes the Si wafer 2102, the inhibition layer 2104, the Ge crystal layer 2106, and the compound semiconductor 2108, which is a GaAs layer, for example. In the present exemplary embodiment, an intermediate layer was formed between the Ge crystal layer 2106 and the compound semiconductor 2108. In the present exemplary embodiment, the planar shape of the covering region was a square with a side of 200 μm. The shape of the bottom of the opening 105 was a square with a side of 10 μm. After the Ge crystal layer 2106 having the thickness of 850 nm was formed by CVD within the opening 105, the Ge crystal layer 2106 was annealed at the temperature of 800° C.
After the Ge crystal layer 2106 was annealed, the temperature of the Si wafer 2102 on which the Ge crystal layer 2106 was formed was controlled to become 550° C., and the intermediate layer was then formed by MOCVD. The intermediate layer was grown by using trimethyl gallium and arsine as the source gases. The intermediate layer had the thickness of 30 nm. Subsequently, the temperature of the Si wafer 2102 on which the intermediate layer was formed was raised to 640° C., and the GaAs layer was formed by MOCVD as an example of the compound semiconductor 2108. The GaAs layer had the thickness of 500 nm. Except for these conditions, the semiconductor wafer was fabricated under the same conditions as in Exemplary Embodiment 9.
In accordance with the same procedure as in Exemplary Embodiment 13, the semiconductor wafer was fabricated that includes the Si wafer 2102, the inhibition layer 2104, the Ge crystal layer 2106, the intermediate layer, and the compound semiconductor 2108, which is a GaAs layer, for example. After this, the fabricated semiconductor wafer was utilized to fabricate an HST element structure. The HBT element structure was fabricated according to the following procedure. To begin with, the semiconductor wafer was fabricated in accordance with the same procedure as in Exemplary Embodiment 13. In the present exemplary embodiment, the planar shape of the covering region was a square with a side of 50 μm. The shape of the bottom of the opening 105 was a square with a side of 20 μm. Except for these conditions, the semiconductor wafer was fabricated under the same conditions as in Exemplary Embodiment 13.
Subsequently, semiconductor layers were formed by MOCVD on the surface of the GaAs layer of the fabricated semiconductor wafer. In this manner, the HBT element structure was provided that includes the Si wafer 2102, the Ge crystal layer 2106 having the thickness of 850 nm, the intermediate layer having the thickness of 30 nm, the undoped GaAs layer having the thickness of 500 nm, an n-type GaAs layer having the thickness of 300 nm, an n-type InGaP layer having the thickness of 20 nm, an n-type GaAs layer having the thickness of 3 nm, a GaAs layer having the thickness of 300 nm, a p-type GaAs layer having the thickness of 50 nm, an n-type InGaP layer having the thickness of 20 nm, an n-type GaAs layer having the thickness of 120 nm, and an n-type InGaAs layer having the thickness of 60 nm in the stated order. Furthermore, electrodes are disposed on the fabricated HBT element structure. Thus, an HBT element was fabricated as an exemplary electronic element or device. To form the semiconductor layers, Si was used as the n-type impurity. To form the semiconductor layers, C was used as the p-type impurity.
In accordance with the same procedure as in Exemplary Embodiment 14, three HBT elements having the same structure as the HST element fabricated in Exemplary Embodiment 14 were fabricated. The fabricated three HBT elements were connected to each other in parallel. In the present exemplary embodiment, the planar shape of the covering region was a rectangle with a long side of 100 μm and a short side of 50 μm. In the covering region, three openings 105 were formed. All the openings 105 were shaped at the bottom as a square with a side of 15 μm. Except for these conditions, the HBT elements were fabricated under the same conditions as in Exemplary Embodiment 14.
HBT elements were fabricated while the area of the bottom of the opening 105 was varied. In this manner, it was examined how the electrical characteristics of the fabricated HBT element were dependent on the area of the bottom of the opening 105. The HBT elements were fabricated in accordance with the same procedure as in Exemplary Embodiment 14. The measured electrical characteristics of the HBT element included the base sheet resistance Rb [Ω/□] and the current gain β. The current gain β was calculated by dividing the value of the collector current by the value of the base current. In the present exemplary embodiment, HBT elements were fabricated with the shape of the bottom of the opening 105 being varied between a square with a side of 20 μm, a rectangle with a short side of 20 μm and a long side of 40 μm, a square with a side of 30 μm, a rectangle with a short side of 30 μm and a long side of 40 μm, and a rectangle with a short side of 20 μm and a long side of 80 μm.
When the shape of the bottom of the opening 105 was a square, the opening 105 was formed such that one of the two sides of the shape of the bottom of the opening 105 that are perpendicular to each other extended in parallel to the <010> direction of the Si wafer 2102 and the other side extended in parallel to the <001> direction of the Si wafer 2102. When the shape of the bottom of the opening 105 was a rectangle, the opening 105 was formed such that the long side of the shape of the bottom of the opening 105 extended in the parallel direction to the <010> direction of the Si wafer 2102 and the short side extended in the parallel direction to the <001> direction of the Si wafer 2102. The planar shape of the covering region was mainly set to a square with a side of 300 μm.
This tells that devices with excellent electrical characteristics can be fabricated by locally forming the HBT element structure on the surface of the Si wafer 2102. In particular, it has been proved that devices with excellent electrical characteristics can be fabricated when the bottom of the opening 105 has a shape with a side of 80 μm or less, or has an area of 1600 μm2 or less. In this case, the bottom of the seed crystal formed within the opening 105 similarly has a maximum width of 80 μm or less, or has an area of 1600 μm2 or less. Here, the maximum width of the bottom of the seed crystal is defined as the length of the longest straight light connecting between any two points on the bottom of the seed crystal.
As described above, a semiconductor wafer could be fabricated by a method of manufacturing a semiconductor wafer, including: a step of forming, on a main plane of a Si wafer, an inhibition layer that inhibits crystal growth; a step of forming, in the inhibition layer, an opening that penetrates through the inhibition layer in a substantially perpendicular direction to the main plane of the wafer to reach the wafer by patterning the inhibition layer; a step of growing a Ge layer within the opening in contact with the wafer and a step of growing a functional layer on the Ge layer. A semiconductor wafer could be fabricated by a method of manufacturing a semiconductor wafer, including: a step of forming an inhibition layer on a Si wafer where the inhibition layer has an opening and inhibits crystal growth; a step of forming a Ge layer within the opening; and a step of forming a functional layer after the Ge layer is formed.
As described above, a semiconductor wafer could be fabricated by forming on a main plane of a Si wafer an inhibition layer that inhibits crystal growth, forming in the inhibition layer an opening that penetrates through the inhibition layer in a substantially perpendicular direction to the main plane of the wafer to reach the wafer, forming a Ge layer by crystal growth within the opening in contact with the wafer, and forming a functional layer by crystal growth on the Ge layer. A semiconductor wafer could be fabricated that includes a Si wafer, an inhibition layer that is provided on the wafer, that has an opening, and that inhibits crystal growth, a Ge layer that is formed within the opening, and a functional layer that is formed after the Ge layer is formed.
As described above, an electronic device could be fabricated by forming on a main plane of a Si wafer an inhibition layer that inhibits crystal growth, forming in the inhibition layer an opening that penetrates through the inhibition layer in a substantially perpendicular direction to the main plane of the wafer to reach the wafer, forming a Ge layer by crystal growth within the opening in contact with the wafer, forming a functional layer by crystal growth on the Ge layer, and forming an electronic element in the functional layer. An electronic device could be fabricated that includes a Si wafer, an inhibition layer that is provided on the wafer, that has an opening, and that inhibits crystal growth, a Ge layer that is formed within the opening, a functional layer that is formed after the Ge layer is formed, and an electronic element that is formed in the functional layer.
On the Ge crystal 2206, a GaAs crystal 2208 was grown to form a seed compound semiconductor by MOCVD using trimethyl gallium and arsine as the source. The GaAs crystal 2208 was equivalent to the seed compound semiconductor crystal 108. The growth of the GaAs crystal 2208 included low-temperature growth at the temperature of 550° C. followed by growth at the temperature of 640° C. During the growth at the temperature of 640° C., the partial pressure of arsine was set at 0.05 kPa. It can be confirmed that the GaAs crystal 2208 is grown on the Ge crystal 2206. It can be confirmed that the (110) plane appears as the seed plane of the GaAs crystal 2208.
Subsequently, the GaAs crystal 2208 was further laterally grown as a laterally grown compound semiconductor layer. During the lateral growth, the temperature was set at 640° C. and the partial pressure of arsine was set at 0.43 kPa.
A semiconductor wafer was fabricated by selectively growing the Ge crystal 2206 on the Si wafer 2202 in accordance with the same procedure as in Exemplary Embodiment 17. The fabricated semiconductor wafer was subjected to cycle annealing in which annealing at the temperature of 800° C. and annealing at the temperature of 680° C. were repeated at 10 times. The resulting semiconductor wafer (hereinafter, referred to as the sample A) was evaluated in terms of the Si element concentration and the Ge element concentration at the boundary between the Ge crystal 2206 and the Si wafer 2202 by using an energy dispersive X-ray fluorescence spectrometer (hereinafter, may be referred to as EDX). Likewise, a semiconductor wafer that was manufactured by selectively growing a Ge crystal on the Si wafer 2202 but did not go through the cycle annealing (hereinafter, referred to as the sample B) was evaluated by the EDX in a similar manner.
The Si element intensity integral value and the Ge element intensity integral value were measured in a limited measured region of the samples A and B. The measured region is defined as the boundary between the Si wafer 2202 and the Ge crystal 2206.
In the region in which the Si wafer 2202 is in contact with the SiO2 film 2204, the Si element profile in the depth direction is plotted. In this region, the boundary between the Si wafer 2202 and the Ge crystal is defined such that, at the boundary, the total of the Si intensity in the Si wafer 2202 and the Si intensity in the SiO2 film 2204 reaches 50%. Then, in the region that is in the Si wafer 2202 and extends between the distance of 5 μm and the distance of 10 nm from the above-defined boundary, the Ge and Si element intensity ratios were respectively measured. Based on the measured element intensity ratios, the Ge element intensity integral value and the Si element intensity integral value were calculated in the depth direction and the ratio between the integral values (Ge/Si) was calculated.
The resulting ratio was 3.33 for the sample A and 1.10 for the sample B. Thus, the average Ge concentration within the region that is in the Si wafer 2202 and extends between the distance of 5 nm and the distance of 10 nm from the boundary between the Si wafer 2202 and the Ge crystal 2206 was 77% in the sample A and 52% in the sample B. The samples A and B were examined in terms of dislocations by using a transmission electron microscope. The examination revealed that no dislocations reached the surface of the Ge crystal 2206 in the sample A. On the other hand, the examination found that the sample B included dislocations that reach the crystal surface with the density of approximately 1×109 cm−2. Consequently, it was confirmed that cycle annealing effectively reduced the dislocations in the Ge crystal 2206.
A sample C was fabricated in such a manner that the GaAs crystal 2208 was grown by MOCVD on the Ge crystal 2206, which has been subjected to the cycle annealing similarly to the sample A of Exemplary Embodiment 18, and that a multilayer structure film constituted by a GaAs layer and an InGaP layer was stacked on the GaAs crystal 2208. Furthermore, a sample D was fabricated by forming the GaAs crystal 2208 and the multilayer structure film in the same manner as above except for that the Ge crystal 2206 did not go through the post annealing.
The samples C and D were evaluated by using an EDX in the same manner as in Exemplary Embodiment 18. Specifically speaking, the Ge and Si element intensity ratios were measured in the region that is in the Si wafer 2202 and extends between the distance of 5 nm and the distance of 10 nm from the boundary between the Si susbtrate 2202 and the Ge crystal. Furthermore, the Ge element intensity integral value and the Si element intensity integral value were calculated in the depth direction and the ratio between the integral values (Ge/Si) was calculated. The resulting ratio was 2.28 for the sample C and 0.60 for the sample D. Thus, the average Ge concentration within the region that is in the Si wafer 2202 and extends between the distance of 5 nm and the distance of 10 μm from the boundary between the Si wafer 2202 and the Ge crystal was 70% in the sample C and 38% in the sample D.
The samples C and D were examined in terms of dislocations by using a transmission electron microscope. The examination revealed that no dislocations reached the multilayer structure film constituted by the GaAs layer and the InGaP layer in the sample C. On the other hand, the examination found that the sample D included dislocations that reach the multilayer structure film constituted by the GaAs layer and the InGaP layer. As is apparent from the above, when the average Ge concentration is 60% or higher in the region that is in the Si wafer 2202 and extends between the distance of 5 nm and the distance of 10 nm from the boundary between the Si wafer 2202 and the Ge crystal, a compound semiconductor layer with a higher quality can be formed on the Ge crystal. The average Ge concentration is more preferably 70% or higher.
Exemplary Embodiment 20 demonstrates that the growth rate of a device forming thin film may vary according to the width of an inhibition layer with reference to the experimental data provided by the named inventors. Here, the device forming thin film indicates a thin film that is processed to constitute a part of a semiconductor device. For example, when a semiconductor device is formed by sequentially stacking a plurality of compound semiconductor thin films on a silicon crystal and processing the stacked compound semiconductor thin films, the device forming thin film includes the stacked compound semiconductor thin films. Furthermore, the device forming thin film also includes a buffer layer formed between the silicon crystal and the stacked compound semiconductor thin films and also includes a seed layer that is used as a nucleus of the crystal growth of the buffer layer or the compound semiconductor thin films.
The growth rate of the device forming thin film determines the characteristics of the device forming thin film such as flatness and crystallinity. The characteristics of the device forming thin film in turn strongly affect the capability of the semiconductor device to be formed in the device forming thin film Therefore, the growth rate of the device forming thin film needs to be appropriately controlled to satisfy the characteristic requirements of the device forming thin film that are derived from the specification requirements of the semiconductor device. The following experimental data indicates that the growth rate of the device forming thin film varies according to the width of the inhibition layer and other parameters. By using the following experimental data, the shape of the inhibition layer can be designed in a manner to achieve an appropriate growth rate of the device forming thin film that is derived from the specification requirements of the device forming thin film.
The inhibition layer 3002 was formed so as to have a substantially square outline and have a substantially square opening at the center of the square. The length of the side a of the opening was set at 30 μm or 50 μm. The width b of the inhibition layer 3002, which is defined as the distance between the outer periphery of the inhibition layer 3002 and the inner periphery of the inhibition layer 3002 varied within the range of 5 μm to 20 μm. The inhibition layer 3002 was made of silicon dioxide (SiO2). No crystals are epitaxially grown on the surface of the silicon dioxide layer when the epitaxial growth conditions were adapted to realize selective MOCVD. The inhibition layer 3002 was formed by, after forming a silicon dioxide film on a base wafer by dry thermal oxidization, patterning the silicon dioxide film by photolithography.
A compound semiconductor crystal was selectively epitaxially grown by MOCVD on a portion of the base wafer in which the inhibition layer 3002 was not formed. The compound semiconductor crystal that is epitaxially grown in the opening surrounded by the inhibition layer 3002 constitutes the device-forming thin film 3004, and the compound semiconductor crystal that externally surrounds the inhibition layer 3002 constitutes the sacrificial growth portion 3006. The compound semiconductor crystal was a GaAs crystal, an InGaP crystal, or a p-type doped GaAs crystal (p-GaAs crystal). The Ga source was trimethyl gallium (Ga(CH3)3) and the As source was arsine (AsH3). The In source was trimethyl indium (In(CH3)3) and the P source was phosphine (PH3). Doping with carbon (C), which served as p-type impurities, was controlled by adjusting the added amount of bromotrichloromethane (CBrCl3), which served as dopants. The epitaxial growth was carried out at the temperature of 610° C.
In
In
As seen from
The above-described experimental results can be explained when the following crystal growth mechanism is taken into consideration. The Ga and As atoms, from which the deposited crystals are formed, are thought to be supplied by the molecules that fly from a space or move over a surface. The named inventors of the present invention think that the dominant supply source is the molecules that move over a surface in the case of the reaction environment in which selective epitaxial growth takes place based on MOCVD. Specifically speaking, the source molecules (precursors) that fly to the inhibition layer 3002, excluding some escaping from the surface, migrate along the surface of the inhibition layer 3002 to be supplied to the device forming thin film 3004 or the sacrificial growth portion 3006. Here, as the width of the inhibition layer 3002 increases, the absolute number of the source molecules supplied by the surface migration increases, thereby increasing the growth rate of the device forming thin film 3004. Also, as the ratio of the area of the device forming thin film 3004 to the total area decreases, the source molecules supplied from the inhibition layer 3002 to the device forming thin film 3004 relatively increases. This results in a higher growth rate of the device forming thin film 3004.
Bearing the above-described growth mechanism in mind, the function of the sacrificial growth portion 3006 can be understood as follows. If the sacrificial growth portion 3006 is not provided, the source molecules are excessively supplied to the device forming thin film 3004. This will disturb the surface of the device forming thin film 3004 and degrade the crystallinity of the device forming thin film 3004. In other words, the sacrificial growth portion 3006 serves to take in an appropriate portion of the source molecules that fly to the inhibition layer 3002, thereby appropriately controlling the amount of the source molecules supplied to the device forming thin film 3004. Stated differently, the sacrificial growth portion 3006 serves to prevent the source molecules from being excessively supplied to the device forming thin film 3004 by consuming some of the source molecules through sacrificial growth.
As seen from
The collectors of the 20 HBT elements 3150 were connected in parallel by means of a collector interconnection 3124, the emitters were connected in parallel by means of an emitter interconnection 3126, and the bases were connected in parallel by means of base interconnections 3128. Note that the 20 bases were divided into four groups, so that five bases of each group were connected in parallel. The collector interconnection 3124 was connected to collector pads 3130, the emitter interconnection 3126 was connected to emitter pads 3132, and the base interconnections 3128 were connected to base pads 3134. The collector interconnection 3124, the collector pads 3130, the emitter interconnection 3126, and the emitter pads 3132 were formed in the same first interconnection layer, and the base interconnections 3128 and the base pads 3134 were formed in a second interconnection layer, which was above the first interconnection layer.
As shown in
As shown in
As shown in
As shown in
In the above description, a MOSFET (metal-oxide-semiconductor filed-effect transistor) is taken as an example of the electronic device. The electronic device, however, is not limited to a MOSFET, but also may be a HEMT (High Electron Mobility Transistor), or a pseudomorphic-HEMT. Furthermore, the electronic device 100 can be, for example, a MESFET (Metal-Semiconductor Field Effect Transistor) or the like.
Although some aspects of the present invention have been described by way of exemplary embodiments, it should be understood that those skilled in the art might make many changes and substitutions without departing from the spirit and the scope of the present invention which is defined only by the appended claims.
The claims, specification and drawings describe the processes of an apparatus, a system, a program and a method by using the terms such as operations, procedures, steps and stages. When a reference is made to the execution order of the processes, wording such as “before” or “prior to” is not explicitly used. The processes may be performed in any order unless an output of a particular process is used by the following process. In the claims, specification and drawings, a flow of operations may be explained by using the terms such as “first” and “next” for the sake of convenience. This, however, does not necessarily indicate that the operations should be performed in the explained order.
The specification may describe that the respective components are sequentially stacked “on” each other or in the upward direction. However, the stacking direction of the electronic device 100 and the like is not limited to the direction from the downside to the upside that are defined in terms of the orientation of the electronic device 100 and the like during their actually usage. As used herein, when a first component is “formed on” a second component, the first component is formed on the second component in terms of the stacking direction. Furthermore, when a first component is “formed on” a second component, the first component may be in contact with the second component, or alternatively, the first component may be formed on the second component with one or more intervening layers formed therebetween.
10 semiconductor wafer, 11 main plane, 12 base wafer, 13 insulating layer, 14 Si crystal layer, 16 seed crystal, 18 compound semiconductor, 19 surface, 20 semiconductor wafer, 25 inhibition layer, 26 seed crystal, 27 opening, 28 compound semiconductor, 30 semiconductor wafer, 34 Si crystal layer, 36 seed crystal, 38 compound semiconductor, 40 semiconductor wafer, 41 plane, 43 upper plane, 44 Si crystal layer, 45 inhibition layer, 46 seed crystal, 48 compound semiconductor, 100 electronic device, 102 SOI wafer, 104 inhibition layer, 105 opening, 106 Ge crystal layer, 108 seed compound semiconductor crystal, 110 first compound semiconductor crystal, 112 second compound semiconductor crystal, 114 gate insulator, 116 gate electrode, 118 source/drain electrode, 120 defect trap, 130 defect trap, 162 Si wafer, 164 insulating layer, 166 Si crystal layer, 172 main plane, 200 electronic device, 300 electronic device, 400 electronic device, 402 buffer layer, 500 electronic device, 502 source/drain electrode, 600 electronic device, 602 source/drain electrode, 700 electronic device, 702 lower gate insulator, 704 lower gate electrode, 801 semiconductor wafer, 802 SOI wafer, 803 region, 804 inhibition layer, 806 opening, 808 collector electrode, 810 emitter electrode, 812 base electrode, 820 Ge crystal layer, 822 buffer layer, 824 compound semiconductor functional layer, 862 Si wafer, 864 insulating layer, 866 Si crystal layer, 872 main plane, 880 MISFET, 882 well, 888 gate electrode, 1101 semiconductor wafer, 1102 SDI wafer, 1108 collector electrode, 1110 emitter electrode, 1112 base electrode, 1120 Ge crystal layer, 1122 InGaP layer, 1123 InGaP layer, 1124 compound semiconductor functional layer, 1125 accompanying layer, 1130 Ge film, 1162 Si wafer, 1164 insulating layer, 1166 Si crystal layer, 1172 main plane, 1201 semiconductor wafer, 1202 seed crystal layer, 1204 GaAs layer, 1301 semiconductor wafer, 2102 Si wafer, 2104 inhibition layer, 2106 Ge crystal layer, 2108 compound semiconductor, 2202 Si wafer, 2204 SiO2 film, 2206 Ge crystal, 2208 GaAs crystal, 3000 semiconductor device forming wafer, 3002 inhibition layer, 3004 device forming thin film, 3006 sacrificial growth portion, 3100 HBT, 3102 inhibition layer, 3108 device forming thin film, 3110 sacrificial growth portion, 3112 emitter electrode, 3114 base electrode, 3116 collector electrode, 3118 field insulating film, 3120 interconnection, 3122 interconnection, 3124 collector interconnection, 3126 emitter interconnection, 3128 base interconnection, 3130 collector pad, 3132 emitter pad, 3134 base pad, 3150 HBT element, 3202 range, 3204 range, 3206 range, 3208 range, 3210 range, 3212 range, 3220 silicon, 3224 buffer layer, 3226 sub-collector layer, 3230 base layer, 3232 emitter layer, 3234 collector electrode, 3236 base electrode, 3238 emitter electrode
Number | Date | Country | Kind |
---|---|---|---|
2008-257857 | Oct 2008 | JP | national |
2008-334830 | Dec 2008 | JP | national |
2009-046587 | Feb 2009 | JP | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
---|---|---|---|---|
PCT/JP2009/005067 | 10/1/2009 | WO | 00 | 3/31/2011 |