SEMICONDUCTOR DEVICE
20230123210 · 2023-04-20
Inventors
Cpc classification
H01L21/02565
ELECTRICITY
H01L21/02483
ELECTRICITY
H01L29/04
ELECTRICITY
H01L21/0262
ELECTRICITY
H01L29/66969
ELECTRICITY
H01L29/0661
ELECTRICITY
H01L29/24
ELECTRICITY
H01L29/0619
ELECTRICITY
International classification
H01L29/06
ELECTRICITY
H01L29/04
ELECTRICITY
H01L29/24
ELECTRICITY
H01L29/66
ELECTRICITY
Abstract
Provided is a semiconductor device including: a semiconductor layer; a non-conductive layer that is in contact with at least a part of a side surface of the semiconductor layer directly or via another layer; and a Schottky electrode that is disposed on the semiconductor layer and the non-conductive layer, an end portion of the Schottky electrode being located above the non-conductive layer.
Claims
1. A semiconductor device comprising: a semiconductor layer; a non-conductive layer that is in contact with at least a part of a side surface of the semiconductor layer directly or via another layer; and a Schottky electrode that is disposed on the semiconductor layer and the non-conductive layer, an end portion of the Schottky electrode being located above the non-conductive layer.
2. The semiconductor device according to claim 1, wherein the non-conductive layer includes a first surface on a side of the Schottky electrode, a second surface that is located on a side opposite to the first surface, and a side surface that is located between the first surface and the second surface, the semiconductor layer includes a first surface on the side of the Schottky electrode, a second surface that is located on the side opposite to the first surface, and the side surface that is located between the first surface and the second surface, and the second surface of the semiconductor layer and the second surface of the non-conductive layer are in the same plane.
3. The semiconductor device according to claim 1, wherein the non-conductive layer includes a first surface on a side of the Schottky electrode, a second surface that is located on a side opposite to the first surface, and a side surface that is located between the first surface and the second surface, the semiconductor layer includes a first surface on the side of the Schottky electrode, a second surface that is located on the side opposite to the first surface, and the side surface that is located between the first surface and the second surface, and the second surface of the non-conductive layer is located at a position closer to the Schottky electrode than the second surface of the semiconductor layer.
4. The semiconductor device according to claim 1, wherein the semiconductor layer contains at least gallium.
5. The semiconductor device according to claim 1, wherein the semiconductor layer contains a crystalline metal oxide as a major component.
6. The semiconductor device according to claim 1, wherein the semiconductor layer contains a mixed crystal of crystalline gallium oxide or gallium oxide.
7. The semiconductor device according to claim 1, wherein the semiconductor layer has a corundum structure.
8. The semiconductor device according to claim 1, wherein the semiconductor layer includes a first surface on a side of the Schottky electrode and a second surface that is located on a side opposite to the first surface, the non-conductive layer includes a first surface on the side of the Schottky electrode and a second surface that is located on the side opposite to the first surface, and the first surface of the semiconductor layer and the first surface of the non-conductive layer are in the same plane.
9. The semiconductor device according to claim 1, wherein the semiconductor layer includes a first surface on a side of the Schottky electrode and a second surface that is located on a side opposite to the first surface, the non-conductive layer includes a first surface on the side of the Schottky electrode and a second surface that is located on the side opposite to the first surface, and the first surface of the semiconductor layer is located at a higher position than the first surface of the non-conductive layer.
10. The semiconductor device according to claim 1, wherein the semiconductor layer includes a first surface on a side of the Schottky electrode and a second surface that is located on a side opposite to the first surface, the non-conductive layer includes a first surface on the side of the Schottky electrode and a second surface that is located on the side opposite to the first surface, and the first surface of the non-conductive layer is located at a higher position than the first surface of the semiconductor layer.
11. The semiconductor device according to claim 1, wherein the side surface of the semiconductor layer includes an inclined surface.
12. The semiconductor device according to claim 11, wherein the semiconductor layer includes a first surface on a side of the Schottky electrode and a second surface that is located on a side opposite to the first surface and includes the side surface that is located between the first surface and the second surface, and the inclined surface of the semiconductor layer is an inclined surface with a film thickness increasing from the first surface toward the second surface.
13. The semiconductor device according to claim 11, wherein the semiconductor layer includes a first surface on a side of the Schottky electrode and a second surface that is located on a side opposite to the first surface and includes the side surface that is located between the first surface and the second surface, and an angle formed by the first surface of the semiconductor layer and the inclined surface of the semiconductor layer is equal to or greater than 20° and equal to or less than 70°.
14. The semiconductor device according to claim 11, wherein the non-conductive layer includes a first inclined surface, the side surface of the semiconductor layer includes the inclined surface as a second inclined surface inclined in a direction opposite to a direction of the first inclined surface, and the first inclined surface of the non-conductive layer and the second inclined surface of the semiconductor layer are engaged.
15. The semiconductor device according to claim 1, wherein at least a part of the side surface of the semiconductor layer is in close contact with the non-conductive layer.
16. The semiconductor device according to claim 1, wherein at least a part of the side surface of the semiconductor layer is in close contact with the non-conductive layer via a protective film.
17. The semiconductor device according to claim 1, wherein the non-conductive layer is an insulating layer.
18. The semiconductor device according to claim 17, wherein the insulating layer is made of at least one selected from silicon dioxide (Si02) and silicon nitride (Si.sub.3N.sub.4).
19. A semiconductor system comprising at least: a semiconductor device, wherein the semiconductor device is the semiconductor device according to claim 1.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION
[0038] The inventors of the present disclosure find out that concentration of an electric field at an end portion of a Schottky electrode may be effectively curbed if a semiconductor layer, a non-conductive layer with which at least a part of a side surface of the semiconductor layer is in contact directly or via another layer, and a Schottky electrode that is disposed on the semiconductor layer and the non-conductive layer are included, and an end portion of the Schottky electrode is disposed to be located above the non-conductive layer.
[0039] Embodiments of the present disclosure will be described below with reference to the accompanying drawings. In the following description, the same parts and components are designated by the same reference numerals. The present embodiment includes, for example, the following disclosures.
Structure 1
[0040] A semiconductor device including: a semiconductor layer; a non-conductive layer that is in contact with at least a part of a side surface of the semiconductor layer directly or via another layer; and a Schottky electrode that is disposed on the semiconductor layer and the non-conductive layer, an end portion of the Schottky electrode being located above the non-conductive layer.
Structure 2
[0041] The semiconductor device according to [Structure 1], wherein the non-conductive layer includes a first surface on a side of the Schottky electrode, a second surface that is located on a side opposite to the first surface, and a side surface that is located between the first surface and the second surface, the semiconductor layer includes a first surface on the side of the Schottky electrode, a second surface that is located on the side opposite to the first surface, and the side surface that is located between the first surface and the second surface, and the second surface of the semiconductor layer and the second surface of the non-conductive layer are in the same plane.
Structure 3
[0042] The semiconductor device according to [Structure 1], wherein the non-conductive layer includes a first surface on a side of the Schottky electrode, a second surface that is located on a side opposite to the first surface, and a side surface that is located between the first surface and the second surface, the semiconductor layer includes a first surface on the side of the Schottky electrode, a second surface that is located on the side opposite to the first surface, and the side surface that is located between the first surface and the second surface, and the second surface of the non-conductive layer is located at a position closer to the Schottky electrode than the second surface of the semiconductor layer.
Structure 4
[0043] The semiconductor device according to any one of [Structure 1] to [Structure 3], wherein the semiconductor layer contains at least gallium.
Structure 5
[0044] The semiconductor device according to any one of [Structure 1] to [Structure 4], wherein the semiconductor layer contains a crystalline metal oxide as a major component.
Structure 6
[0045] The semiconductor device according to any one of [Structure 1] to [Structure 5], wherein the semiconductor layer contains a mixed crystal of crystalline gallium oxide or gallium oxide.
Structure 7
[0046] The semiconductor device according to any one of [Structure 1] to [Structure 6], wherein the semiconductor layer has a corundum structure.
Structure 8
[0047] The semiconductor device according to any one of [Structure 1] to [Structure 7], wherein the semiconductor layer includes a first surface on a side of the Schottky electrode and a second surface that is located on a side opposite to the first surface, the non-conductive layer includes a first surface on the side of the Schottky electrode and a second surface that is located on the side opposite to the first surface, and the first surface of the semiconductor layer and the first surface of the non-conductive layer are in the same plane.
Structure 9
[0048] The semiconductor device according to any one of [Structure 1] to [Structure 7], wherein the semiconductor layer includes a first surface on a side of the Schottky electrode and a second surface that is located on a side opposite to the first surface, the non-conductive layer includes a first surface on the side of the Schottky electrode and a second surface that is located on the side opposite to the first surface, and the first surface of the semiconductor layer is located at a higher position than the first surface of the non-conductive layer.
Structure 10
[0049] The semiconductor device according to any one of [Structure 1] to [Structure 7], wherein the semiconductor layer includes a first surface on a side of the Schottky electrode and a second surface that is located on a side opposite to the first surface, the non-conductive layer includes a first surface on the side of the Schottky electrode and a second surface that is located on the side opposite to the first surface, and the first surface of the non-conductive layer is located at a higher position than the first surface of the semiconductor layer.
Structure 11
[0050] The semiconductor device according to any one of [Structure 1] to [Structure 10], wherein the side surface of the semiconductor layer includes an inclined surface.
Structure 12
[0051] The semiconductor device according to [Structure 11], wherein the semiconductor layer includes a first surface on a side of the Schottky electrode and a second surface that is located on a side opposite to the first surface and includes the side surface that is located between the first surface and the second surface, and the inclined surface of the semiconductor layer is an inclined surface with a film thickness increasing from the first surface toward the second surface.
Structure 13
[0052] The semiconductor device according to [Structure 11] or [Structure 12], wherein the semiconductor layer includes a first surface on a side of the Schottky electrode and a second surface that is located on a side opposite to the first surface and includes the side surface that is located between the first surface and the second surface, and an angle formed by the first surface of the semiconductor layer and the inclined surface of the semiconductor layer is equal to or greater than 20 ° and equal to or less than 70 °.
Structure 14
[0053] The semiconductor device according to any one of [Structure 11] to [Structure 13], wherein the non-conductive layer includes a first inclined surface, the side surface of the semiconductor layer includes the inclined surface as a second inclined surface inclined in a direction opposite to a direction of the first inclined surface, and the first inclined surface of the non-conductive layer and the second inclined surface of the semiconductor layer are engaged.
Structure 15
[0054] The semiconductor device according to any one of [Structure 1] to [Structure 14], wherein at least a part of the side surface of the semiconductor layer is in close contact with the non-conductive layer.
Structure 16
[0055] The semiconductor device according to any one of [Structure 1] to [Structure 14], wherein at least a part of the side surface of the semiconductor layer is in close contact with the non-conductive layer via a protective film.
Structure 17
[0056] The semiconductor device according to any one of [Structure 1] to [Structure 16], wherein the non-conductive layer is an insulating layer.
Structure 18
[0057] The semiconductor device according to [Structure 17], wherein the insulating layer is made of at least one selected from silicon dioxide (SiO.sub.2) and silicon nitride (Si.sub.3N.sub.4).
Structure 19
[0058] A semiconductor system including at least: a semiconductor device, wherein the semiconductor device is the semiconductor device according to any one of [Structure 1] to [Structure 18].
[0059] Although embodiments of the present disclosure will be described below using the drawings, the present disclosure is not limited thereto and may include combinations of elements in the exemplified embodiments and other elements. As one embodiment of the present disclosure,
[0060] The semiconductor layer may contain, as a major component, a nitride semiconductor of gallium nitride containing, for example, silicon carbide, gallium nitride, indium nitride, aluminum nitride, and mixed crystals thereof or may contain a crystalline metal oxide as a major component. In the present embodiment, the semiconductor layer preferably contains at least gallium. Also, in the present embodiment, the semiconductor layer preferably contains a crystalline metal oxide as a major component and more preferably contains a mixed crystal of crystalline gallium oxide or gallium oxide. Note that the “major component” means that in a case where the semiconductor layer contains α-Ga.sub.2O.sub.3 as a major component, for example, it is only necessary for α-Ga.sub.2O.sub.3 to be contained at a proportion of equal to or greater than 0.5 in terms of an atomic ratio of gallium in metal elements in the semiconductor layer. In the present disclosure, the atomic ratio of gallium in the metal elements in the semiconductor layer is preferably equal to or greater than 0.7 and is more preferably equal to or greater than 0.8.
[0061] The non-conductive layer is made of a material with a higher electrical resistivity than a high-resistant layer and is typically a semi-insulating layer or an insulating layer, and in the embodiment of the present disclosure, the non-conductive layer is preferably an insulating layer. Examples of the semi-insulating layer include polysilicon (polycrystalline silicon), amorphous silicon, diamond-like carbon (DLC), and the like. Also, examples of the material of the insulating layer include oxide, nitride, carbide, and the like such as silicon dioxide (SiO.sub.2), silicon nitride (Si.sub.3N.sub.4), silicon (Si), germanium (Ge), titanium (Ti), zirconium (Zr), Hf (Hafnium), Ta (tantalum), and tin (Sn). Curbing of concentration of an electric field may be more effectively expressed by combining the preferable insulating layer as described above with a bevel structure, which will be described later.
[0062] Also,
[0063] In addition,
[0064] Additionally,
[0065] Furthermore,
[0066] In the embodiment of the manufacturing method of present disclosure, a film formation method of the semiconductor layer (hereinafter, also referred to as the semiconductor film) is not particularly limited as long as the film formation method is able to cause the semiconductor layer to epitaxially grow. Examples of the film formation method of the semiconductor layer include at least one method selected from a spray method, mist CVD, HVPE, MBE, MOCVD, and a sputtering process.
[0067] An example of a method of forming the semiconductor layer using HVPE shown in
Metal Source
[0068] The metal source is not limited to a particular metal source as long as the metal source contains metal and can be gasified, and may be elemental metal or a metal compound. Examples of the metal include one or two or more types of metal selected from gallium, aluminum, indium, iron, chromium, vanadium, titanium, rhodium, nickel, cobalt, iridium and so forth. In the present disclosure, the metal is preferably one or two or more types of metal selected from gallium, aluminum, and indium and more preferably gallium, and the metal source is most preferably elemental gallium. Moreover, the metal source may be gas, liquid, or solid; in the present disclosure, when gallium is used as the metal, for example, it is preferable that the metal source is liquid.
[0069] A means for the gasification is not limited to a particular means unless it interferes with the object of the present disclosure, and may be a publicly known means. In the present disclosure, it is preferable that the means for the gasification is performed by halogenating the metal source. A halogenating agent that is used in the halogenation is not limited to a particular halogenating agent as long as the halogenating agent can halogenate the metal source, and may be a publicly known halogenating agent. Examples of the halogenating agent include halogens, hydrogen halides or the like. Examples of the halogens include fluorine, chlorine, bromine, iodine or the like. Moreover, examples of the hydrogen halides include hydrogen fluoride, hydrogen chloride, hydrogen bromide, and hydrogen iodide. In the present disclosure, a hydrogen halide is preferably used in the halogenation and hydrogen chloride is more preferably used in the halogenation. In the present disclosure, it is preferable that the gasification is performed by supplying a halogen or hydrogen halide to the metal source as a halogenating agent and making the metal source and the halogen or hydrogen halide react with each other at a temperature equal to or higher than a vaporization temperature of a metal halide to form a metal halide. The halogenation reaction temperature is not limited to a particular temperature; in the present disclosure, when, for example, the metal source is gallium and the halogenating agent is HCl, the halogenation reaction temperature is preferably 900° C. or lower, more preferably 700° C. or lower, and most preferably 400 to 700° C. The metal-containing source gas is not limited to particular metal-containing source gas as long as the metal-containing source gas is gas containing the metal of the metal source. Examples of the metal-containing source gas include a halide (such as fluoride, chloride, bromide, or iodide) of the metal.
[0070] In an embodiment of the present disclosure, after a metal source containing metal is gasified to obtain metal-containing source gas, the metal-containing source gas and the oxygen-containing source gas are supplied to the space above a substrate inside the reaction chamber. Moreover, in an embodiment of the present disclosure, reactive gas is supplied to the space above the substrate. Examples of the oxygen-containing source gas include O.sub.2 gas, CO.sub.2 gas, NO gas, NO.sub.2 gas, N.sub.2O gas, H.sub.2O gas, O.sub.3 gas or the like. In the present disclosure, the oxygen-containing source gas is preferably one or two or more types of gas selected from a group consisting of O.sub.2, H.sub.2O, and N.sub.2O and more preferably contains O.sub.2. It is to be noted that the oxygen-containing source gas may contain CO.sub.2 as one of embodiments. The reactive gas is generally reactive gas that is different from metal-containing source gas and oxygen-containing source gas and inert gas is not included therein. The reactive gas is not limited to particular reactive gas and examples thereof include etching gas. The etching gas is not limited to particular etching gas unless it interferes with the object of the present disclosure, and may be publicly known etching gas. In the present disclosure, the reactive gas is preferably halogen gas (for example, fluorine gas, chlorine gas, bromine gas, or iodine gas), hydrogen halide gas (for example, hydrofluoric acid gas, hydrochloric acid gas, hydrobromic gas, and hydrogen iodide gas), hydrogen gas, mixed gas of two or more of these gases, or the like, preferably contains hydrogen halide gas, and most preferably contains hydrogen chloride. It is to be noted that the metal-containing source gas, the oxygen-containing source gas, and the reactive gas may contain carrier gas. Examples of the carrier gas include inert gas such as nitrogen and argon. Moreover, the partial pressure of the metal-containing source gas is not limited to a particular partial pressure; in the present disclosure, the partial pressure of the metal-containing source gas is preferably 0.5 Pa to 1 kPa and more preferably 5 Pa to 0.5 kPa. The partial pressure of the oxygen-containing source gas is not limited to a particular partial pressure; in the present disclosure, the partial pressure of the oxygen-containing source gas is preferably 0.5 to 100 times higher than the partial pressure of the metal-containing source gas and more preferably 1 to 20 times higher than the partial pressure of the metal-containing source gas. The partial pressure of the reactive gas is also not limited to a particular partial pressure; in an embodiment of the present disclosure, the partial pressure of the reactive gas is preferably 0.1 to 5 times higher than the partial pressure of the metal-containing source gas and more preferably 0.2 to 3 times higher than the partial pressure of the metal-containing source gas.
[0071] In an embodiment of the present disclosure, it is also preferable to supply dopant-containing gas to the substrate. The dopant-containing gas is not limited to particular dopant-containing gas as long as the dopant-containing gas contains dopant. The dopant is also not limited to particular dopant; in the present disclosure, the dopant preferably contains one or two or more types of elements selected from germanium, silicon, titanium, zirconium, vanadium, niobium, and tin, more preferably contains germanium, silicon, or tin, and most preferably contains germanium. By using the dopant-containing gas as described above, it is possible to easily control the conductivity of a film to be obtained. The dopant-containing gas preferably contains the dopant in the form of a compound (for example, a halide or oxide) and more preferably contains the dopant in the form of a halide. The partial pressure of the dopant-containing gas is not limited to a particular partial pressure; in the present disclosure, the partial pressure of the dopant-containing gas is preferably 1×10.sup.-7 to 0.1 times higher than the partial pressure of the metal-containing source gas and more preferably 2.5×10.sup.-6 to 7.5×10.sup.-2 times higher than the partial pressure of the metal-containing source gas. It is to be noted that, in the present disclosure, it is preferable to supply the dopant-containing gas to the space above the substrate along with the reactive gas.
[0072] As another example mentioned later, at least a part of the semiconductor film and/or base in the embodiment of the present disclosure may be formed by such a mist CVD device shown in
Base
[0073] The base is not particularly limited as long as the base is able to support the mask and/or the semiconductor film. The material of the base is not particularly limited unless it interferes with the present disclosure, a known base may be used, and the material of the base may be an organic compound or may be an inorganic compound. The shape of the base may be any shape and is effective for any shape, examples thereof include a plate shape such as a flat plate or a disk, a fiber shape, a rod shape, a columnar shape, a prismatic shape, a tubular shape, a spiral shape, a spherical shape, and a ring shape, and a substrate is preferable in one embodiment of the present disclosure. Also, the base preferably includes a crystalline layer in another embodiment of the present disclosure. The crystalline layer may be a semiconductor layer. As illustrated in
Crystalline Substrate
[0074] When the substrate includes a crystalline substrate or is the crystalline substrate, The crystalline substrate is not limited to a particular crystalline substrate as long as the crystalline substrate is a substrate containing a crystalline substance as a major component, and may be a publicly known substrate. The crystalline substrate may be an insulator substrate, a conductive substrate, or a semiconductor substrate. The crystalline substrate may be a monocrystalline substrate or a polycrystalline substrate. Examples of the crystalline substrate include a silicon carbide (SiC) substrate, a gallium nitride (GaN) substrate, a substrate containing a crystal substance having a corundum structure as a major component, a substrate containing a crystal substance having a β-gallia structure as a major component, a substrate having a hexagonal structure, or the like. It is to be noted that the “major component” refers to the crystal substance constituting 50% or more, preferably 70% or more, and more preferably 90% or more of the substrate in terms of composition ratio.
[0075] Examples of the substrate containing a corundum-structured crystal as a major component include a sapphire (α-Al.sub.2O.sub.3) substrate and an α-phase gallium oxide (α-Ga.sub.2O.sub.3) substrate. Examples of the substrate containing a β-gallia-structured crystal as a major component include p-phase gallium oxide β-Ga.sub.2O.sub.3) substrate and a substrate containing a mixed crystal of β—Ga.sub.2O.sub.3 and α—Al.sub.2O.sub.3. As a substrate containing the mixed crystal of β—Ga.sub.2O.sub.3 and α—Al.sub.2O.sub.3, the substrate of the mixed crystal in which Al.sub.2O.sub.3 is contained in a range of more than 0% to 60% or less in terms of atomic ratio. Also, examples of the hexagonal-structured substrate include a silicon carbide (SiC) substrate, a zinc oxide (ZnO) substrate, a gallium nitride (GaN) substrate. An example of another crystalline substrate is a silicon (Si) substrate, for example.
[0076] In an embodiment of the present disclosure, it is preferable that the crystalline substrate is a sapphire substrate. Examples of the sapphire substrate include a c-plane sapphire substrate, an m-plane sapphire substrate and an a-plane sapphire substrate. The sapphire substrate may include an off-angle. The off-angle of the sapphire substrate is not particularly limited, however, preferably in a range of 0° to 15°. Also, the thickness of the crystalline substrate is not particularly limited, however preferably in a range of 50 .Math.m to 2000 .Math.m, and further preferably in a range of 200 .Math.m to 800 .Math.m.
[0077]
[0078]
[0079] In addition, the mask 12 may also be used as the insulating layer 62 of the semiconductor device 100 illustrated in
[0080]
[0081] Note that in regard to the semiconductor film 14, the first surface 14a of the semiconductor film 14 may be formed at a lower position than the first surface 12a of the mask 12 as illustrated in
[0082] The semiconductor film includes the first surface 14a, the second surface 14b on the side opposite to the first surface 14a, and the inclined surface 14c that is located between the first surface 14a and the second surface 14b, the mask 12 includes the first surface 12a, the second surface 12b on the side opposite to the first surface 12a, and the side surface including the inclined surface 12c that is located between the first surface 12a and the second surface 12b, and further, the first surface 14a of the semiconductor film 14 may be formed at a lower position than the first surface 12a of the mask 12. Note that a p type semiconductor film may also be caused to epitaxially grow on the first surface 14a of the semiconductor film 14 after the semiconductor film 14 is caused to epitaxially grow as an n- type semiconductor as illustrated in
[0083] Also, according to another embodiment of the present disclosure, the semiconductor film 14 may also be formed such that the first surface 14a of the semiconductor film 14 and the first surface 12a of the mask 12 are at the same height as illustrated in
[0084] In the present embodiment, the inclined surface of the semiconductor film 14 and the inclined surface of the mask 12 are in close contact with each other. In this case, the electrode 15 is formed to cover at least a part of the first surface 14a of the semiconductor film 14 and at least a part of the first surface 12a of the mask 12 as illustrated in
[0085] Furthermore, the first surface 14a of the semiconductor film 14 may be formed at a higher position than the first surface 12a of the mask 12 as illustrated in
[0086] Furthermore, the first surface 14a of the semiconductor film 14 may be formed at a lower position than the first surface 12a of the mask 12 as illustrated in
[0087] A diagrammatic view of results of simulating electric field distribution at 100 V in a case where Ga.sub.2O.sub.3 is used as the semiconductor film (n- type semiconductor layer) 64, Ga.sub.2O.sub.3 is used as the second semiconductor layer (n+ type semiconductor layer) 67, SiO.sub.2 is used as the non-conductive layer (insulating layer) 62, and the inclination angle 64e is set to 29° in the semiconductor device 100 in
[0088] In comparison with the simulation of the semiconductor device with the structure in
[0089] In the embodiment of the present disclosure, a buffer layer including a stress buffering layer or the like may be provided at least as a part of the base on the substrate, and in the case where the buffer layer is provided, the recessed and projecting portions may be formed even on the buffer layer. Also, in the embodiment of the present disclosure, the substrate preferably includes the buffer layer at a part or entirety of the surface thereof. A means for forming the buffer layer is not particularly limited and may be a known means. Examples of the formation means include a spray method, a mist CVD method, an HVPE method, an MBE method, an MOCVD method, and a sputtering method. The buffer layer is formed by the mist CVD method in the present disclosure, which is preferable since more excellent film quality of the crystalline film formed on the buffer layer may be achieved and particularly, a crystal defect such as tilting may be curbed. Hereinafter, a suitable mode in which the buffer layer is formed by the mist CVD method will be described in more detail.
[0090] The buffer layer may be formed suitably by atomizing a raw material solution to obtain atomized liquid droplets (atomizing process), transporting the obtained atomized liquid droplets to the substrate using carrier gas (transport process), and causing a thermal reaction of the atomized liquid droplets (a mist or liquid droplets)by a part or entirety of the surface of the substrate and/or the base (buffer layer formation process), for example.
Atomization Process
[0091] The atomization process atomizes the raw material solution and obtains the atomized droplets. The means of atomizing the raw material solution is not limited to a particular means as long as the means can atomize the raw material solution, and may be a publicly known means; in the present disclosure, an atomizing means using ultrasonic waves is preferable. The atomized droplets obtained using ultrasonic waves are preferable because the initial velocity thereof is zero, which allows them to be suspended in the air, and are very suitable because they are mist that is suspended in the space and can be conveyed as gas, not being sprayed like a spray, for example, and therefore cause no damage by collision energy. The droplet size is not limited to a particular size and may be a droplet of about a few mm; the droplet size is preferably 50 .Math.m or less and more preferably 0.1 to 10 .Math.m.
Raw Material Solution
[0092] The raw material solution is not limited to a particular raw material solution as long as the raw material solution is a solution and allows the buffer layer, the crystalline layer and/or the semiconductor layer to be obtained by mist CVD. Examples of the raw material solution include an aqueous solution of an organometallic complex (for example, an acetylacetonato complex) or a halide (for example, fluoride, chloride, bromide, or iodide) of metal for atomization. The metal for atomization is not limited to particular metal, and examples of such metal for atomization include one or two or more types of metal selected from aluminum, gallium, indium, iron, chromium, vanadium, titanium, rhodium, nickel, cobalt, iridium and so forth. In the present disclosure, the metal for atomization preferably contains at least gallium, indium, or aluminum and more preferably contains at least gallium. The content of the metal for atomization in the raw material solution is not limited to a particular content unless it interferes with the object of the present disclosure; the content of the metal for atomization in the raw material solution is preferably 0.001 to 50 mol% and more preferably 0.01 to 50 mol%.
[0093] Moreover, it is also preferable that the raw material solution contains dopant. By making the raw material solution contain dopant, it is possible to easily control the electrical conductivity of the buffer layer, the crystalline layer and/or the semiconductor layer without a breakdown of a crystal structure without performing ion implantation or the like. In the present disclosure, the dopant is preferably tin, germanium, or silicon, more preferably tin or germanium, and most preferably tin. In general, the concentration of the dopant may be about 1×10.sup.16/cm.sup.3 to 1×10.sup.22/cm.sup.3; the concentration of the dopant may be set at a low concentration of about 1×10.sup.17/cm.sup.3 or less or the raw material solution may be made to contain the dopant at a high concentration of about 1×10.sup.20/cm.sup.3 or more. In the present disclosure, the concentration of the dopant is preferably 1×10.sup.20/cm.sup.3 or less and more preferably 5×10.sup.19/cm.sup.3 or less.
[0094] A solvent of the raw material solution is not limited to a particular solvent and may be an inorganic solvent such as water, an organic solvent such as alcohol, or a mixed solvent of an inorganic solvent and an organic solvent. In the present disclosure, the solvent preferably contains water, is more preferably water or a mixed solvent of water and alcohol, and is most preferably water. More specifically, examples of the water include pure water, ultrapure water, tap water, well water, mineral water, mineralized water, hot spring water, spring water, fresh water, and seawater; in the present disclosure, ultrapure water is preferable.
Conveying Process
[0095] In the conveying process, the atomized droplets are conveyed into a film formation chamber by carrier gas. The carrier gas is not limited to particular carrier gas unless it interferes with the object of the present disclosure, and suitable examples of the carrier gas include oxygen, ozone, inert gas such as nitrogen and argon, reducing gas such as hydrogen gas and forming gas, or the like. Moreover, one type of carrier gas may be used; two or more types of carrier gas may be used and dilution gas (for example, 10-fold dilution gas) with a decreased flow rate, for example, may be additionally used as second carrier gas. Furthermore, instead of one carrier gas supply point, two or more carrier gas supply points may be provided. The flow rate of carrier gas is not limited to a particular flow rate and is preferably 0.01 to 20 L/min and more preferably 1 to 10 L/min. When dilution gas is used, the flow rate of the dilution gas is preferably 0.001 to 2 L/min and more preferably 0.1 to 1 L/min.
Formation Process of Buffer Layer, Crystalline Layer, and/or Semiconductor Layer
[0096] In the formation process of the buffer layer, the crystalline layer, and/or the semiconductor layer (hereinafter, also referred to as a crystalline layer), the crystalline layer is formed on the substrate by causing a thermal reaction of the atomized liquid droplets inside the film formation chamber. The thermal reaction may be any thermal reaction as long as the mist or the liquid droplets thermally cause a reaction, and reaction conditions and the like are also not particularly limited unless they interfere with the present disclosure. In this process, the thermal reaction is typically caused at a temperature that is equal to or greater than a solvent evaporation temperature, the temperature is preferably equal to or less than a temperature that is not excessively high (1000° C., for example), is more preferably equal to or less than 650° C., and is most preferably from 400° C. to 650° C. Also, although the thermal reaction may be caused in any atmosphere out of under vacuum, in a non-oxygen atmosphere, in a reducing gas atmosphere, and in an oxygen atmosphere and may be caused under any condition out of under an atmospheric pressure, under a pressure, and under a reduced pressure unless it interferes with the present disclosure, the thermal reaction is preferably caused under an atmospheric pressure in the present disclosure. Note that the thickness of the crystalline layer may be set by adjusting the formation time.
[0097] The crystalline layer may be formed as a buffer layer on a part or entirety of the surface of the substrate to obtain a base, the aforementioned mask may be disposed on the crystalline layer of the base, and the semiconductor film may be caused to epitaxially grow as described above. Since the recessed/projecting portions are provided on the substrate and the crystalline layer is then formed when the base is prepared, the crystalline layer including lateral growth may be obtained, a defect such as tilting in the crystalline layer as the buffer layer may be further reduced, and more excellent film quality is achieved, by forming the crystalline layer. Also, the crystalline layer may also be used as the semiconductor layer of the semiconductor device as described above, and further excellent film quality of the semiconductor film may be achieved by forming the semiconductor film having a bevel structure on the semiconductor layer.
[0098] Also, although the crystalline layer is not particularly limited, the crystalline layer preferably contains a metal oxide as a major component in one embodiment of the present disclosure. Examples of the metal oxide include metal oxides or the like containing one kind or two or more kinds of metal selected from aluminum, gallium, indium, iron, chromium, vanadium, titanium, rhodium, nickel, cobalt, iridium, and the like. In the present disclosure, the metal oxide preferably contains one kind or two or more kinds of elements selected from indium, aluminum, and gallium, more preferably contains at least indium or/and gallium, and most preferably contains at least gallium. According to one embodiment of the film formation method of the present disclosure, the buffer layer may contain a metal oxide as a major component, and the metal oxide included in the buffer layer may contain gallium and aluminum in a smaller amount than the amount of gallium. Also, according to one embodiment of the film formation method of the present disclosure, the buffer layer may include a superlattice structure. Note that the “major component” in the present disclosure means that preferably not less than 50%, more preferably not less than 70%, and further preferably not less than 90% of the metal oxide is contained with respect to all components in the buffer layer in terms of an atomic ratio and means that the content of the metal oxide may be 100%. Although the crystal structure of the metal oxide is not particularly limited, the crystal structure is preferably a corundum structure or a β-gallia structure and is more preferably a corundum structure according to one embodiment of the present disclosure. Also, although the crystalline film and the buffer layer may have mutually the same major component or different major components unless it interferes with the present disclosure, the crystalline film and the buffer layer preferably have mutually the same major component in the embodiment of the present disclosure.
[0099] The semiconductor film obtained by the manufacturing method according to the present disclosure may be suitably used for a semiconductor device, in particular, and is especially useful for a power device. Examples of the semiconductor device formed using the crystalline film include transistors and TFTs such as MIS and HEMT, Schottky barrier diodes and junction barrier Schottky diodes using semiconductor-metal junctions, and the like. In the embodiment of the present disclosure, there is an advantage that the semiconductor film may be used for a semiconductor device or the like as it is by causing the semiconductor film to epitaxially grow on a base with the mask formed thereon. Also, the semiconductor film may be applied to a semiconductor device or the like after a known means such as peeling-off from the base or the like is used.
[0100] The semiconductor device according to the present disclosure is suitably used as a power module, an inverter, or a converter by further using a known method in addition to the above items, and further, the semiconductor device is suitably used for a semiconductor system using a power supply device, for example. The power supply device may be produced by connecting the semiconductor device to a wiring pattern or the like by using a known method.
Example
[0101] Although an example of the present disclosure will be described below, the present disclosure is not limited thereto.
Example
1. Preparation of Base (Formation of Buffer Layer)
1-1. Mist CVD Device
[0102] A mist CVD device 19 used in the present example will be described using
1-2. Production of Raw Material Solution (Formation of Buffer Layer)
[0103] Gallium acetylacetonate was mixed into ultrapure water, the aqueous solution was adjusted to contain 0.05 mol/L of gallium acetylacetonate, and at this time, 5% of hydrobromic acid was caused to be contained in terms of a volume ratio, and this was obtained as a raw material solution.
1-3. Preparation for Film Formation (Formation of Buffer Layer)
[0104] The raw material solution 24a obtained in 1-2 above was accommodated in the mist generation source 24. Then, as a film formation target 20, a sapphire substrate was placed on the hot plate 28, the hot plate 28 was caused to operate, and the temperature of the film formation target was raised to 550° C. Next, the flow regulating valves 23a and 23b were opened to supply carrier gas from the carrier gas sources 22a and carrier gas (diluted) source 22b into the film formation chamber 30, the atmosphere in the film formation chamber 30 was sufficiently substituted with the carrier gas, and the flow rate of the carrier gas and the flow rate of the carrier gas (diluted) were then adjusted to 0.8 L/min and 0.2 L/min, respectively. Note that oxygen was used as the carrier gas.
1-4. Film Formation (Formation of Buffer Layer)
[0105] Next, the ultrasonic vibrator 26 was caused to vibrate at 2.4 MHz, the vibration was caused to propagate to the raw material solution 24a through the water 25a, the raw material solution 24a was thereby atomized, and fine raw material particles were generated. The fine raw material particles were introduced into the film formation chamber 30 by the carrier gas and caused reaction inside the film formation chamber 30 at 550° C., and a buffer layer (Ga.sub.2O.sub.3 buffer layer having a corundum structure) was formed on the substrate 20, thereby obtaining a base. Note that the film formation time was 10 minutes and the film thickness was 0.1 .Math.m.
2. Formation of Mask
2-1. Formation of Mask Layer
[0106] A mask layer of silicon oxide (SiO.sub.2) was formed on the buffer layer obtained in 1-4 described above using liquid tetraethyl orthosilicate by a plasma enhanced CVD method. The film thickness of the mask layer was 1.3 .Math.m.
2-2. Formation of Photoresist Layer
[0107] A photoresist layer was formed on at least a part of the mask layer obtained in 2-1 described above by photolithography.
2-3. Formation of Mask Having Inclined Surface
[0108] An opening portion was formed in the SiO.sub.2 mask layer having the photoresist layer obtained in 2-2 described above using a buffered hydrofluoric acid (BHF) at a room temperature. The opening portion in the mask layer having the inclined surface at an end portion is formed by undercut of isotropic wet etching. The angle (inclination angle) formed between the surface of the mask layer in contact with the base and the inclined surface was formed at 29°, and a base with the mask including the inclined surface disposed thereon was obtained.
3. Formation of Semiconductor Film
3-1. Film Formation Device
[0109] A device capable of causing epitaxial growth may be used as the film formation device according to the embodiment of the present disclosure, and the mist CVD device illustrated in
3-2. Production of Raw Material Solution (Formation of Semiconductor Film)
[0110] Gallium bromide was mixed into ultrapure water, the aqueous solution was adjusted to contain 0.05 mol/L of gallium, and at this time, 20% of hydrobromic acid was caused to be contained in terms of a volume ratio, and this was obtained as a raw material solution.
3-3. Preparation for Film Formation (Formation of Semiconductor Film)
[0111] The raw material solution 24a obtained in 3-2 described above was accommodated in the mist generation source 24. Next, the base which was obtained in 2-3 and included the mask including the inclined surface disposed thereon was placed as the film formation target 20 on the hot plate 28, and the temperature of the base was raised to 630° C. Then, the flow regulating valves 23a and 23b were opened to supply carrier gas from the carrier gas source 22a and the carrier gas (diluted) source 22b into the film formation chamber 30, the atmosphere in the film formation chamber 30 was sufficiently substituted with the carrier gas, and the flow rate of the carrier gas and the flow rate of the carrier gas (diluted) were then adjusted to 0.8 L/min and 0.2 L/min, respectively. Note that nitrogen was used as the carrier gas.
3-4. Film Formation (Formation of Semiconductor Film)
[0112] Next, the ultrasonic vibrator 26 was caused to vibrate at 2.4 MHz, the vibration was caused to propagate to the raw material solution 24a through the water 25a, the raw material solution 24a was thereby atomized, and fine raw material particles were generated. The fine raw material particles were introduced into the film formation chamber 30 by the carrier gas and caused reaction inside the film formation chamber 30 at 630° C., and a semiconductor film was formed on the base 20 which was obtained in 2-3 described above and included the mask including the inclined surface disposed thereon. Note that the film formation time was 3.5 hours.
3-5. Evaluation
[0113] The semiconductor film obtained in 3-4 described above was a well-tuned film with no cracking and abnormal growth. The obtained film was subjected to 2θ/ω scanning at an angle of 15 degrees to 95 degrees using a thin-film XRD diffracting device, and the film was identified. Measurement was performed using CuKα radiation. As a result, the thus obtained film was α—Ga.sub.2O.sub.3. Also, an inclined surface was formed at the end portion of the semiconductor film of α—Ga.sub.2O.sub.3 as illustrated in
Industrial Applicability
[0114] Although the manufacturing method according to the present disclosure may be used in any fields of semiconductors (for example, compound semiconductor electronic devices and the like), electronic components and electrical equipment components, optical and electrophotography-related devices, industrial members, and the like, the manufacturing method is particularly useful for manufacturing and the like of semiconductor devices including Schottky junctions and semiconductor devices including power semiconductors used for power supplies or the like.
[0115] The embodiments of the present invention are exemplified in all respects, and the scope of the present invention includes all modifications within the meaning and scope equivalent to the scope of claims.
Reference Signs List
[0116] 11 Base [0117] 11a First surface of base [0118] 11b Second surface of base [0119] 12 Mask [0120] 12a First surface of mask [0121] 12b Second surface of mask [0122] 12c Inclined surface of mask [0123] 12d Opening portion of mask [0124] 12e Inclination angle of mask [0125] 12′ Second mask [0126] 13 Protective film [0127] 14 Semiconductor film [0128] 14a First surface of semiconductor film [0129] 14b Second surface of semiconductor film [0130] 14c Inclined surface of semiconductor film [0131] 15 Electrode [0132] 15c End portion of electrode 15 [0133] 16 Substrate [0134] 17 Crystalline layer [0135] 18 Crystalline layer [0136] 19 Mist CVD device [0137] 20 Film formation target [0138] 22a Carrier gas source [0139] 22b Carrier gas (diluted) source [0140] 23a Flow regulating valve [0141] 23b Flow regulating valve [0142] 24 Mist generation source [0143] 24a Raw material solution [0144] 25 Container [0145] 25a Water [0146] 26 Ultrasonic vibrator [0147] 27 Supply pipe [0148] 28 Hot plate [0149] 30 Film formation chamber [0150] 50 Halide vapor phase epitaxy (HVPE) device [0151] 51 Reaction chamber [0152] 52a Heater [0153] 52b Heater [0154] 53a Halogen-containing raw material gas supply source [0155] 53b Metal-containing raw material gas supply pipe [0156] 54a Reactive gas supply source [0157] 54b Reactive gas supply pipe [0158] 55a Oxygen-containing raw material gas supply source [0159] 55b Oxygen-containing raw material gas supply pipe [0160] 56 Substrate holder [0161] 57 Metal source [0162] 58 Protective sheet [0163] 59 Gas discharge portion [0164] 61 Crystalline layer [0165] 62 Non-conductive layer [0166] 62a First surface of non-conductive layer 62 [0167] 62b Second surface of non-conductive layer 62 [0168] 62c Inclined surface of non-conductive layer 62 [0169] 63 Protective film [0170] 64 Semiconductor film [0171] 64a First surface of semiconductor film [0172] 64b Second surface of semiconductor film [0173] 64c Inclined surface of semiconductor film [0174] 64e Inclination angle formed by first surface 64a and inclined surface 64c of semiconductor film [0175] 64f First region of semiconductor film [0176] 64g Second region of semiconductor film [0177] 65 First electrode [0178] 65c End portion of first electrode [0179] 66 Second electrode [0180] 67 p type semiconductor portion [0181] 90 Rectifier junction interface [0182] 100 Semiconductor device [0183] 170 Power supply system [0184] 171 Power supply device [0185] 172 Power supply device [0186] 173 Control circuit [0187] 180 System device [0188] 181 Electronic circuit [0189] 182 Power supply system [0190] 192 Inverter [0191] 193 Transformer [0192] 194 MOSFET [0193] 195 DCL [0194] 196 PWM control circuit [0195] 197 Voltage comparator [0196] 200 Semiconductor device [0197] 300 Semiconductor device [0198] 400 Semiconductor device [0199] 500 Semiconductor device