WO2024055885A1 - Semiconductor device and preparation method therefor - Google Patents

Semiconductor device and preparation method therefor Download PDF

Info

Publication number
WO2024055885A1
WO2024055885A1 PCT/CN2023/117298 CN2023117298W WO2024055885A1 WO 2024055885 A1 WO2024055885 A1 WO 2024055885A1 CN 2023117298 W CN2023117298 W CN 2023117298W WO 2024055885 A1 WO2024055885 A1 WO 2024055885A1
Authority
WO
WIPO (PCT)
Prior art keywords
layer
groove
semiconductor device
doped
silicon
Prior art date
Application number
PCT/CN2023/117298
Other languages
French (fr)
Chinese (zh)
Inventor
苏帅
何林峰
魏巍
张亚文
武龙
侯明辰
冯鹏
韩明涛
李皓天
周瑞
Original Assignee
华为技术有限公司
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 华为技术有限公司 filed Critical 华为技术有限公司
Publication of WO2024055885A1 publication Critical patent/WO2024055885A1/en

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/04Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
    • H01L21/18Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
    • H01L21/30Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
    • H01L21/324Thermal treatment for modifying the properties of semiconductor bodies, e.g. annealing, sintering
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L29/00Semiconductor devices specially adapted for rectifying, amplifying, oscillating or switching and having potential barriers; Capacitors or resistors having potential barriers, e.g. a PN-junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof ; Multistep manufacturing processes therefor
    • H01L29/40Electrodes ; Multistep manufacturing processes therefor
    • H01L29/43Electrodes ; Multistep manufacturing processes therefor characterised by the materials of which they are formed
    • H01L29/45Ohmic electrodes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L29/00Semiconductor devices specially adapted for rectifying, amplifying, oscillating or switching and having potential barriers; Capacitors or resistors having potential barriers, e.g. a PN-junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof ; Multistep manufacturing processes therefor
    • H01L29/66Types of semiconductor device ; Multistep manufacturing processes therefor
    • H01L29/66007Multistep manufacturing processes
    • H01L29/66075Multistep manufacturing processes of devices having semiconductor bodies comprising group 14 or group 13/15 materials
    • H01L29/66227Multistep manufacturing processes of devices having semiconductor bodies comprising group 14 or group 13/15 materials the devices being controllable only by the electric current supplied or the electric potential applied, to an electrode which does not carry the current to be rectified, amplified or switched, e.g. three-terminal devices
    • H01L29/66409Unipolar field-effect transistors
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L29/00Semiconductor devices specially adapted for rectifying, amplifying, oscillating or switching and having potential barriers; Capacitors or resistors having potential barriers, e.g. a PN-junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof ; Multistep manufacturing processes therefor
    • H01L29/66Types of semiconductor device ; Multistep manufacturing processes therefor
    • H01L29/68Types of semiconductor device ; Multistep manufacturing processes therefor controllable by only the electric current supplied, or only the electric potential applied, to an electrode which does not carry the current to be rectified, amplified or switched
    • H01L29/76Unipolar devices, e.g. field effect transistors
    • H01L29/772Field effect transistors
    • H01L29/778Field effect transistors with two-dimensional charge carrier gas channel, e.g. HEMT ; with two-dimensional charge-carrier layer formed at a heterojunction interface

Definitions

  • the present application relates to the field of semiconductor technology, and more specifically, to a semiconductor device and a manufacturing method thereof.
  • semiconductor devices such as high electron mobility transistors, etc.
  • semiconductor devices have been widely used in electronic devices such as mobile phones and tablet computers.
  • Semiconductor devices provided by related technologies often form ohmic contact between the electrode layer and the epitaxial layer through the metal type and ratio of the electrode layer (such as the source layer and the drain layer), the thickness of the epitaxial layer, etc.
  • the resistivity of ohmic contact is high, usually greater than 1 ⁇ mm, which is not conducive to reducing the on-resistance of semiconductor devices.
  • the present application provides a semiconductor device and a preparation method thereof, which realizes ohmic contact between the first electrode layer and the epitaxial layer, reduces the contact resistivity of the ohmic contact, helps to reduce the on-resistance of the semiconductor device, and thereby reduces Power losses in semiconductor devices.
  • the present application provides a semiconductor device, which may include an epitaxial layer, a doping layer, a dielectric layer and a first electrode layer.
  • the epitaxial layer and the dielectric layer can be stacked.
  • the semiconductor device may be provided with a first groove, and a part of the doping layer and the first electrode layer may be stacked inside the first groove. It can be understood that a part of the first electrode may be disposed inside the first groove, and another part of the first electrode may be disposed outside the first groove.
  • the semiconductor device provided by this application forms the ohmic contact between the first electrode layer and the epitaxial layer through the doping layer, which reduces the contact resistivity of the ohmic contact, helps to reduce the on-resistance of the semiconductor device, and thereby reduces the power of the semiconductor device. loss.
  • the doped layer, the epitaxial layer and the first electrode layer are all different, that is, there is a clear boundary between the doped layer and the epitaxial layer, and there is also a clear boundary between the doped layer and the first electrode layer.
  • the material of the doping layer may be any one or more of silicon, silicon oxide, silicon nitride, and silicon oxynitride.
  • the state of the doped layer may be a single crystal state, a polycrystalline state or an amorphous state.
  • the thickness of the doped layer may be 1 nm to 50 nm. Ohmic contact between the first electrode layer and the epitaxial layer can be achieved through the doping layer.
  • the material of the doped layer can also be other materials, and the thickness of the doped layer can also be in other thickness ranges, which is not limited in this application.
  • the thickness of the doped layer from a peak concentration of silicon down to a silicon concentration of 10% may be less than 20 nm.
  • the peak concentration of silicon can be 80%, 70%, 60%, etc. It can be understood that when the concentration of silicon is the peak concentration, the doped layer can correspond to a thickness. In the case of a silicon concentration of 10%, the doped layer can correspond to another thickness. The thickness difference between the two thicknesses may be less than 20 nm, which can reduce the contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer. Of course, the thickness difference between the two thicknesses will change with the concentration of silicon. This application does not limit the thickness of the doped layer from the peak concentration of silicon to a silicon concentration of 10%.
  • the thickness of the doped layer from a first concentration of silicon to a silicon concentration of 10% may be less than 20 nm.
  • the first concentration may be greater than or equal to 60%.
  • the first concentration may be 70% or 60%, etc.
  • the doped layer may correspond to a thickness.
  • the doped layer can correspond to another thickness.
  • the thickness difference between the two thicknesses may be less than 20 nm, which can reduce the contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer. Of course, the thickness difference between the two thicknesses will change with the concentration of silicon. This application does not limit the thickness of the doped layer from the first concentration of silicon to the second concentration of silicon.
  • the epitaxial layer may include a channel layer, a barrier layer and a cap layer that are stacked on the surface of the substrate. That is to say, the substrate, channel layer, barrier layer and cap layer are stacked in sequence.
  • the bottom of the first groove may be located at the cap layer, barrier layer or channel layer. That is to say, the bottom of the first groove can be located on the surface or inside the cap layer, on the surface or inside the barrier layer, or can also be located inside the channel layer. Furthermore, it is possible to make the first electrode layer and The cap layer, barrier layer or channel layer forms an ohmic contact.
  • the distance between the bottom of the first groove and the surface of the channel layer may be within 20 nm.
  • the surface of the channel layer may be used to indicate the surface of the channel layer close to the barrier layer.
  • the bottom of the first groove may be located inside the barrier layer or inside the channel layer. Regardless of whether the bottom of the first groove is located at the bottom of the first groove or inside the barrier layer, the distance between the bottom of the first groove and the surface of the channel layer can be within 20 nm.
  • the ohmic contact between the first electrode layer and the barrier layer can be realized, or the ohmic contact between the first electrode layer and the channel layer can be realized, and the contact resistivity of the ohmic contact can be reduced to the greatest extent, and the contact resistivity can be reduced to 0.5 ⁇ . ⁇ mm, while improving the working efficiency of semiconductor devices, it can also reduce the preparation cost of semiconductor devices.
  • the dielectric layer may be provided with a second groove, and the bottom of the second groove may be located on the surface of the capping layer, wherein the surface of the capping layer may be used to indicate that the capping layer is away from the barrier layer. surface.
  • the semiconductor device may further include a second electrode layer, the second electrode layer may be located inside the second groove, and the second electrode layer and the cap layer may form a Schottky contact.
  • the second electrode layer may be a gate layer. Therefore, the gate layer and the cap layer may form a Schottky contact.
  • the material of the first electrode layer may include any one or more of titanium Ti, gold Au, and aluminum Al.
  • the material of the source layer may include any one or more of titanium Ti, gold Au, and aluminum Al.
  • the material of the drain layer may also include any one or more of titanium Ti, gold Au, and aluminum Al.
  • the materials of the source layer and the drain layer can also be of other types, which are not limited in this application.
  • the material of the second electrode layer may include any one or more of titanium Ti, gold Au, and nickel Ni.
  • the material of the second electrode layer can also be of other types, which is not limited in this application.
  • the present application provides a method for manufacturing a semiconductor device, which can be used to prepare the semiconductor device provided by the first aspect and its possible implementations.
  • the preparation method may include: performing photolithography on the epitaxial layer to form a mask layer.
  • the doped layer is formed according to the mask layer.
  • a first electrode layer is formed on the surface of the doped layer, and the first electrode layer is annealed according to a preset annealing temperature.
  • the preset annealing temperature can be 400°C to 800°C.
  • the preparation method provided by this application has a simple process.
  • the contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer in the prepared semiconductor device is greatly reduced, and the contact resistivity can reach 0.5 ⁇ mm, which improves the working efficiency of the semiconductor device.
  • the manufacturing cost of semiconductor devices can be reduced.
  • photolithography of the epitaxial layer to form a mask layer may include: applying photoresist on the surface of the epitaxial layer, and applying the photoresist to the surface of the epitaxial layer according to the preset baking temperature and preset baking time.
  • the epitaxial layer is baked. Expose the baked epitaxial layer according to the preset exposure time. Use a developing solution and develop the exposed epitaxial layer according to the preset development time to form a mask layer.
  • the preset baking temperature can be 90°C to 120°C.
  • the preset baking time can be 60s to 120s, which can solidify the liquid photoresist on the surface of the epitaxial layer.
  • the preset baking temperature can also be in other temperature ranges, and the preset baking time can also be in other time ranges, which are not limited in this application.
  • the preset exposure time can be 100 ms to 1000 ms, which can transfer the pattern on the mask to the cured photoresist.
  • the preset exposure time can also be in other time ranges, which is not limited in this application.
  • the developer may be a tetramethylammonium hydroxide (TMAH) solution (which may be referred to as a TMAH solution).
  • TMAH tetramethylammonium hydroxide
  • the preset development time can be 30s to 90s, and the pattern on the cured photoresist can be transferred to the epitaxial layer.
  • the developer can also be other solutions, and the preset development time can also be other time ranges, which are not limited in this application.
  • forming the doping layer according to the mask layer may include: forming the doping layer on the surface of the epitaxial layer according to the mask layer. That is to say, the doped layer can be directly formed on the surface of the epitaxial layer according to the mask layer.
  • the preparation method provided by this application may also include: using plasma to process the surface of the epitaxial layer according to a preset processing time. That is to say, after photolithography of the epitaxial layer to form the mask layer, the surface of the epitaxial layer can be processed and then a doped layer can be formed. The surface roughness of the epitaxial layer can be increased, and the contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer can be further reduced.
  • the preset processing time can be 2min ⁇ 60min.
  • the plasma may include any one or more of hydrogen H 2 , nitrogen N 2 , ammonia NH 3 , chlorine Cl 2 , argon Ar and oxygen O 2 .
  • forming the doped layer according to the mask layer may include etching part of the epitaxial layer according to the mask layer to form a first groove. A deposition process is used to form a doped layer inside the first groove.
  • the epitaxial layer may include a channel layer, a barrier layer and a cap layer stacked on the surface of the substrate, then The cap layer is etched according to the mask layer, the cap layer and the barrier layer can be photolithographed according to the mask layer, or the cap layer, barrier layer and channel layer can be etched according to the mask layer. Therefore, the bottom of the first groove may be located on the surface or inside the cap layer, on the surface or inside the barrier layer, or on the surface or inside the channel layer.
  • the doped layer formed inside the first groove may also be located at different positions in the epitaxial layer depending on the position of the bottom of the first groove.
  • the deposition process can include atomic layer deposition (ALD) process (ALD process for short), plasma enhanced atomic layer deposition (PEALD) process (PEALD process for short), plasma enhanced Chemical vapor deposition (plasma enhanced chemical vapor deposition, PECVD) process (referred to as PECVD process), inductively coupled plasma chemical vapor deposition (ICPCVD) process (referred to as ICPCVD process), low pressure chemical vapor deposition (referred to as ICPCVD process) Any one of the low pressure chemical vapor deposition (LPCVD) process (referred to as LPCVD process), the electron beam evaporation (electronic beam evaporation, EBE) process (referred to as EBE process) and the sputtering deposition process.
  • ALD atomic layer deposition
  • PEALD plasma enhanced atomic layer deposition
  • PECVD plasma enhanced Chemical vapor deposition
  • ICPCVD inductively coupled plasma chemical vapor deposition
  • ICPCVD process low pressure chemical vapor deposition
  • the preparation method provided by this application may further include: forming a dielectric layer on the surface of the epitaxial layer. Photolithography and etching are performed on the dielectric layer to form a second groove. A second electrode layer is formed inside the second groove.
  • the doping layer, the epitaxial layer and the first electrode layer are all different. That is, there is a clear boundary between doped layers and epitaxial layers. There is also a clear demarcation between the doped layer and the first electrode layer.
  • the material of the doping layer may be any one or more of silicon, silicon oxide, silicon nitride, and silicon oxynitride.
  • the state of the doped layer may be a single crystal state, a polycrystalline state or an amorphous state.
  • the thickness of the doped layer may be 1 nm to 50 nm. Ohmic contact between the first electrode layer and the epitaxial layer can be achieved through the doping layer.
  • the material of the doped layer can also be other materials, and the thickness of the doped layer can also be in other thickness ranges, which is not limited in this application.
  • the doped layer is less than 20 nm thick from a peak concentration of silicon down to a silicon concentration of 10%.
  • the peak concentration of silicon can be 80%, 70%, 60%, etc. It can be understood that when the concentration of silicon is the peak concentration, the doped layer can correspond to a thickness. In the case of a silicon concentration of 10%, the doped layer can correspond to another thickness.
  • the thickness difference between the two thicknesses may be less than 20 nm, which can reduce the contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer. Of course, the thickness difference between the two thicknesses will change with the concentration of silicon. This application does not limit the thickness of the doped layer from the peak concentration of silicon to a silicon concentration of 10%.
  • the doped layer is less than 20 nm thick from a first concentration of silicon down to a silicon concentration of 10%.
  • the first concentration may be greater than or equal to 60%.
  • the first concentration may be 70% or 60%, etc.
  • the doped layer may correspond to a thickness.
  • the doped layer can correspond to another thickness.
  • the thickness difference between the two thicknesses may be less than 20 nm, which can reduce the contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer. Of course, the thickness difference between the two thicknesses will change with the concentration of silicon. This application does not limit the thickness of the doped layer from the first concentration of silicon to the second concentration of silicon.
  • the present application provides a method for manufacturing a semiconductor device, which can be used to prepare the semiconductor device provided by the first aspect and its possible implementations.
  • the preparation method may include photolithography of the dielectric layer to form a mask layer.
  • the doped layer is formed according to the mask layer.
  • a first electrode layer is formed on the surface of the doped layer, and the first electrode layer is annealed according to a preset annealing temperature.
  • the preset annealing temperature can be 400°C to 800°C.
  • the preparation method provided by this application has a simple process.
  • the contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer in the prepared semiconductor device is greatly reduced, and the contact resistivity can reach 0.5 ⁇ mm, which improves the working efficiency of the semiconductor device.
  • the manufacturing cost of semiconductor devices can be reduced.
  • performing photolithography on the dielectric layer to form a mask layer may include: applying photoresist on the surface of the dielectric layer, and applying the photoresist on the surface of the dielectric layer according to the preset baking temperature and preset baking time.
  • the medium layer is baked. Expose the baked dielectric layer according to the preset exposure time. Use a developing solution and develop the exposed dielectric layer according to the preset development time to form a mask layer.
  • the preset baking temperature can be 90°C to 120°C.
  • the preset baking time can be 60s to 120s, which can solidify the liquid photoresist on the surface of the epitaxial layer.
  • the preset baking temperature can also be in other temperature ranges, and the preset baking time can also be in other time ranges, which are not limited in this application.
  • the preset exposure time can be 100 ms to 1000 ms, which can transfer the pattern on the mask to the cured photoresist.
  • the preset exposure time can also be in other time ranges, which is not limited in this application.
  • the developer may be a tetramethylammonium hydroxide TMAH solution.
  • the preset development time can be 30s to 90s, and the pattern on the cured photoresist can be transferred to the epitaxial layer.
  • the developer can also be other solutions, and the preset development time can also be other time ranges, which are not limited in this application.
  • forming the doping layer according to the mask layer may include: etching the dielectric layer according to the mask layer to form a first groove.
  • the dielectric layer and part of the epitaxial layer are etched according to the mask layer to form a first groove. That is to say, only the dielectric layer can be etched according to the mask layer, or the dielectric layer and part of the epitaxial layer can be etched according to the mask layer, and the first groove can be formed.
  • a deposition process may be used to form a doped layer inside the first groove.
  • the deposition process may include any one of an ALD process, a PEALD process, a PECVD process, an ICPCVD process, a LPCVD process, an EBE process and a sputtering deposition process.
  • the preparation method provided by this application may also include: using plasma to process the surface of the epitaxial layer according to a preset processing time. That is to say, after photolithography of the epitaxial layer to form the mask layer, the surface of the epitaxial layer can be processed and then a doped layer can be formed. The surface roughness of the epitaxial layer can be increased, and the contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer can be further reduced.
  • the preset processing time can be 2min ⁇ 60min.
  • the plasma may include any one or more of hydrogen H 2 , nitrogen N 2 , ammonia NH 3 , chlorine Cl 2 , argon Ar and oxygen O 2 .
  • the preparation method provided by this application may further include: performing photolithography and etching on the dielectric layer to form a second groove.
  • a second electrode layer is formed inside the second groove.
  • the doping layer, the epitaxial layer and the first electrode layer are all different. That is, there is a clear boundary between doped layers and epitaxial layers. There is also a clear demarcation between the doped layer and the first electrode layer.
  • the material of the doping layer may be any one or more of silicon, silicon oxide, silicon nitride, and silicon oxynitride.
  • the state of the doped layer may be a single crystal state, a polycrystalline state or an amorphous state.
  • the thickness of the doped layer may be 1 nm to 50 nm. Ohmic contact between the first electrode layer and the epitaxial layer can be achieved through the doping layer.
  • the material of the doped layer can also be other materials, and the thickness of the doped layer can also be in other thickness ranges, which is not limited in this application.
  • the doped layer is less than 20 nm thick from a peak concentration of silicon down to a silicon concentration of 10%.
  • the peak concentration of silicon can be 80%, 70%, 60%, etc. It can be understood that when the concentration of silicon is the peak concentration, the doped layer can correspond to a thickness. In the case of a silicon concentration of 10%, the doped layer can correspond to another thickness.
  • the thickness difference between the two thicknesses may be less than 20 nm, which can reduce the contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer. Of course, the thickness difference between the two thicknesses will change with the concentration of silicon. This application does not limit the thickness of the doped layer from the peak concentration of silicon to a silicon concentration of 10%.
  • the doped layer is less than 20 nm thick from a first concentration of silicon down to a silicon concentration of 10%.
  • the first concentration may be greater than or equal to 60%.
  • the first concentration may be 70% or 60%, etc.
  • the doped layer may correspond to a thickness.
  • the doped layer can correspond to another thickness.
  • the thickness difference between the two thicknesses may be less than 20 nm, which can reduce the contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer. Of course, the thickness difference between the two thicknesses will change with the concentration of silicon. This application does not limit the thickness of the doped layer from the first concentration of silicon to the second concentration of silicon.
  • the present application provides an electronic chip, which may include passive devices and the semiconductor device provided by the above-mentioned first aspect and its possible implementations.
  • the passive device can be electrically connected to the semiconductor device.
  • passive components may be resistors, capacitors, etc.
  • the passive components can also be other components, which are not limited in this application.
  • the present application provides an electronic device, which may include a circuit board and the electronic chip provided in the fourth aspect and possible implementations thereof.
  • the electronic chip can be arranged on the circuit board.
  • Figure 1 is a schematic structural diagram of a semiconductor device 1 in an embodiment of the present application.
  • Figure 2 is a schematic structural diagram of groove A in the embodiment of the present application.
  • Figure 3 is another schematic structural diagram of groove A in the embodiment of the present application.
  • Figure 4 is another schematic structural diagram of groove A in the embodiment of the present application.
  • Figure 5 is another schematic structural diagram of groove A in the embodiment of the present application.
  • Figure 6 is another schematic structural diagram of groove A in the embodiment of the present application.
  • Figure 7 is another schematic structural diagram of groove A in the embodiment of the present application.
  • Figure 8 is another schematic structural diagram of the semiconductor device 1 in the embodiment of the present application.
  • Figure 9 is a schematic flow chart of a method for manufacturing the semiconductor device 1 in the embodiment of the present application.
  • Figure 10 is a schematic structural diagram of the mask layer 70 formed by photolithography on the epitaxial layer 20 in the embodiment of the present application;
  • Figure 11 is a schematic flow chart of photolithography of the epitaxial layer 20 to form the mask layer 70 in an embodiment of the present application;
  • Figure 12 is a schematic flow chart of forming the doping layer 30 according to the mask layer 70 in the embodiment of the present application;
  • Figure 13 is a schematic structural diagram of etching the epitaxial layer 20 to form a groove A in an embodiment of the present application
  • Figure 14 is a schematic structural diagram of processing groove A in the embodiment of the present application.
  • Figure 15 is a schematic structural diagram of forming the doping layer 30 according to the mask layer 70 in the embodiment of the present application.
  • Figure 16 is another schematic flow chart of forming the doping layer 30 according to the mask layer 70 in the embodiment of the present application.
  • Figure 17 is a schematic structural diagram of processing the surface of the epitaxial layer 20 in the embodiment of the present application.
  • Figure 18 is a schematic structural diagram of forming the doping layer 30 on the surface of the epitaxial layer 20 in the embodiment of the present application;
  • Figure 19 is a schematic structural diagram of forming the electrode layer 50 on the surface of the doped layer 30 in the embodiment of the present application.
  • Figure 20 is a schematic structural diagram of removing the mask layer 70 in the embodiment of the present application.
  • Figure 21 is another schematic structural diagram of removing the mask layer 70 in the embodiment of the present application.
  • Figure 22 is a schematic flow chart for forming the gate layer 60 in an embodiment of the present application.
  • Figure 23 is a schematic structural diagram of forming the dielectric layer 40 in the embodiment of the present application.
  • Figure 24 is a schematic structural diagram of forming groove B in the embodiment of the present application.
  • Figure 25 is another schematic flow chart of the method of manufacturing the semiconductor device 1 in the embodiment of the present application.
  • Figure 26 is another schematic flow chart of the preparation method of the semiconductor device 1 in the embodiment of the present application.
  • Figure 27 is another schematic flow chart of the preparation method of the semiconductor device 1 in the embodiment of the present application.
  • Figure 28 is a schematic structural diagram of forming the dielectric layer 40 on the surface of the epitaxial layer 20 in the embodiment of the present application;
  • Figure 29 is a schematic flow chart of photolithography of the dielectric layer 40 to form the mask layer 70 in an embodiment of the present application
  • Figure 30 is a schematic structural diagram of the mask layer 70 formed by photolithography on the dielectric layer 40 in the embodiment of the present application;
  • Figure 31 is a schematic structural diagram of etching the dielectric layer 40 and part of the epitaxial layer 20 to form a groove A in an embodiment of the present application;
  • Figure 32 is another schematic structural diagram of removing the mask layer 70 in the embodiment of the present application.
  • Figure 33 is another schematic structural diagram of processing groove A in the embodiment of the present application.
  • Figure 34 is a schematic structural diagram of forming the doping layer 30 inside the groove A in the embodiment of the present application.
  • Figure 35 is a schematic structural diagram of etching the dielectric layer 40 to form a groove A in the embodiment of the present application.
  • Figure 36 is another schematic structural diagram of forming the doping layer 30 inside the groove A in the embodiment of the present application.
  • FIG. 37 is another schematic flow chart of a method for manufacturing the semiconductor device 1 in the embodiment of the present application.
  • At least one (item) refers to one or more, and “plurality” refers to two or more.
  • “And/or” is used to describe the relationship between associated objects, indicating that there can be three relationships. For example, “A and/or B” can mean: only A exists, only B exists, and A and B exist simultaneously. , where A and B can be singular or plural. The character “/” generally indicates that the related objects are in an "or” relationship. “At least one of the following” or similar expressions thereof refers to any combination of these items, including any combination of a single item (items) or a plurality of items (items).
  • At least one of a, b or c can mean: a, b, c, "a and b", “a and c", “b and c", or "a and b and c” ”, where a, b, c can be single or multiple.
  • semiconductor devices such as high electron mobility transistors, etc.
  • semiconductor devices have been widely used in electronic devices such as mobile phones and tablet computers.
  • Semiconductor devices provided by related technologies often form ohmic contact between the electrode layer and the epitaxial layer through the metal type and ratio of the electrode layer (such as the source layer and the drain layer), the thickness of the epitaxial layer, etc.
  • the resistivity of ohmic contacts is higher, usually greater than 1 ⁇ mm, which is not conducive to reducing the on-resistance of semiconductor devices.
  • the semiconductor device 1 may include a substrate 10, an epitaxial layer 20, a doped layer 30, a dielectric layer 40 and an electrode layer (ie, a first electrode layer) 50.
  • the electrode layer 50 may include a source layer 51 and a drain layer 52 .
  • the substrate 10, the epitaxial layer 20 and the dielectric layer 40 may be stacked.
  • the epitaxial layer 20 may include a stacked channel layer 21 , a barrier layer 22 and a cap layer 23 , it can also be considered that the substrate 10 , the channel layer 21 , the barrier layer 22 , the cap layer 23 and the dielectric layer 40 are stacked set up.
  • other layers may be disposed in the epitaxial layer 20 , and/or other layers may be disposed between the substrate 10 , the epitaxial layer 20 and the dielectric layer 40 , which are not limited in the embodiments of the present application.
  • the semiconductor device 1 may be provided with a groove A (ie, a first groove, not marked in FIG. 1 ).
  • the doped layer 30 and a part of the electrode layer 50 may be stacked and disposed in the groove A. That is to say, a part of the electrode layer 50 and the doping layer 30 are stacked and arranged in the groove A, and another part of the electrode layer 50 may be arranged outside the groove A. Therefore, the ohmic contact between the electrode layer 50 and the epitaxial layer 20 can be formed through the doped layer 30 .
  • ohmic contact means that when the electrode layer 50 is in contact with the epitaxial layer 20, a very small contact barrier is formed at the contact interface, or no contact barrier is formed at the contact interface. That is, an ohmic contact has a lower contact resistivity. Ohmic contact can also be called non-rectifying contact.
  • the electrode layer 50 may include a source layer 51 and a drain layer 52. Therefore, the semiconductor device 1 may have two grooves A, one of which is used to place the doping layer 30 and the source layer 51. The other is used to place doped layer 30 and drain layer 52.
  • the lower part of the source layer 51 can be stacked with the doping layer 30 and disposed in a groove A, and the upper part of the source layer 51 can be disposed outside the groove A.
  • the lower part of the drain layer 52 may be stacked with the doping layer 30 and disposed in another groove A, and the upper part of the drain layer 52 may be disposed outside the other groove A.
  • the semiconductor device 1 provided by the embodiment of the present application forms an ohmic contact between the electrode layer 50 and the epitaxial layer 20 through the doping layer 30, which reduces the contact resistivity of the ohmic contact, helps to reduce the on-resistance of the semiconductor device, and thereby reduces the Power losses in semiconductor devices.
  • the dielectric layer 40 may be provided with groove B (ie, the second groove, not marked in FIG. 1 ).
  • the bottom of the groove B may be located on the surface of the capping layer 23 .
  • the surface of the cap layer 23 may be used to indicate the surface of the cap layer 23 facing away from the barrier layer 22 , that is, the upper surface of the cap layer 23 in FIG. 1 .
  • the semiconductor device 1 may further include a gate layer 60 (ie, a second electrode layer), and the gate layer 60 may be located inside the groove B.
  • the gate layer 60 and the cap layer 23 may form a Schottky contact. It should be explained that Schottky contact means that when the gate layer 60 and the cap layer 23 are in contact, the energy band of the cap layer 23 bends at the contact interface, forming a contact barrier (which can be called a Schottky barrier). ). Schottky contact can also be called rectifying contact.
  • the doping layer 30 , the epitaxial layer 20 and the electrode layer 50 are all different. That is to say, there is a clear boundary between the doped layer 30 and the epitaxial layer 20 (which can be the cap layer 23, the barrier layer 22 or the channel layer 21). There are also clear boundaries between the doping layer 30 and the electrode layer 50 (ie, the doping layer 30 and the source layer 51, and the doping layer 30 and the drain layer 52).
  • the material of the substrate 10 may be silicon (silicon) (which may be doped silicon or non-doped silicon), silicon carbide (SiC), sapphire (sapphire), and other materials. any one or more of them.
  • the material of the substrate 1 can also be other materials, which are not limited in the embodiments of this application.
  • epitaxial layer 20 may be a portion grown directly on substrate 10 in a semiconductor device process.
  • the thickness of the channel layer 21 in the epitaxial layer 20 may be 100 nm to 500 nm, and the material of the channel layer 21 may be gallium nitride (gallium nitride). Of course, the thickness of the channel layer 21 can also be in other thickness ranges, and the material of the channel layer 21 can also be other materials, which are not limited in the embodiments of this application.
  • the barrier layer 22 in the channel layer 21 and the epitaxial layer 20 can directly generate two-dimensional electron gas (2DEG), as shown in Figure 1 .
  • 2DEG two-dimensional electron gas
  • physical methods such as quantum confinement can be used to limit the movement of the electron group in one direction to a small range, while a system that can move freely in the other two directions is called a two-dimensional electronic system. Therefore, the electrons with lower density in the two-dimensional electron system can be called two-dimensional electron gas.
  • the channel layer 21 can increase the concentration of the two-dimensional electron gas, increase the current density of the semiconductor device 1 , and thereby increase the output current of the semiconductor device 1 .
  • the barrier layer 22 may be made of aluminum gallium nitride (AlGaN), and the barrier layer 22 may have a thickness of 15 nm to 40 nm. Since the materials of the barrier layer 22 and the channel layer 21 are different, they can form a heterojunction.
  • the barrier layer 22 may be made of aluminum gallium nitride AlGaN, and the channel layer 21 may be made of gallium nitride GaN. Thus, a heterojunction can be formed between the barrier layer 22 and the channel layer 21 . Two-dimensional electron gas can be obtained at the interface of the heterojunction.
  • the material of the barrier layer 22 can also be any one of InAlN (indium aluminum nitride), InGaN (indium gallium nitride), and AlInGaN (aluminum indium gallium nitride). , or any combination of the aforementioned materials (including aluminum gallium nitride AlGaN). Therefore, the thickness of the barrier layer 22 may be 5 nm to 20 nm. Similarly, the barrier layer 22 and the channel layer 21 may form a heterojunction.
  • the material of the barrier layer 22 can be other materials, and the thickness of the barrier layer 22 can also be in other thickness ranges, which are not limited in the embodiments of this application.
  • the material of the cap layer 23 in the epitaxial layer 20 may be GaN, and the thickness of the cap layer 23 may be 1 nm to 5 nm.
  • the cap layer 23 can be used to prevent the barrier layer 22 from being oxidized, thereby protecting the interface of the barrier layer 22 .
  • the material of the capping layer 23 can also be other materials, and the thickness of the capping layer 23 can also be in other thickness ranges, which are not limited in the embodiments of this application.
  • the source layer 51 may be made of any one or more of various materials such as titanium (titanium), gold (aurum), and aluminum (Al). That is to say, the source layer 51 may be made of Ti, Au or Al, or may be made of an alloy of at least two metals among Ti, Au and Al.
  • the material of the drain layer 52 may also be any one or more of various materials such as titanium (Titanium), gold (Au) (aurum), and aluminum (Al).
  • the gate layer 60 may be made of any one or more of various materials such as Ti, Au, and nickel (nickel). That is to say, the gate layer 60 may be made of Ti, Au or Ni, or may be made of an alloy of at least two metals among Ti, Au and Ni.
  • the source layer 51 , the drain layer 52 and the gate layer 60 can also be made of other materials, which are not limited in the embodiments of this application.
  • the source layer 51 and the drain layer 52 are made of the same material, and they are alloys of Ti, Al and Au respectively. Moreover, Ti, Al, Ti, and Au can be stacked in the order, and the corresponding thicknesses are 20nm, 150nm, 30nm, and 50nm respectively.
  • the material of the doping layer 30 may be any one or more of Si, silicon oxide SiO 2 (silicon dioxide), silicon nitride SiN (silicon nitride), and silicon oxynitride SiON (silicon oxynitride). kind.
  • the thickness of the doped layer 30 may be 1 nm to 50 nm.
  • the state of the doped layer 30 may be a single crystal state, a polycrystalline state, or an amorphous state.
  • the doped layer 30 can realize the ohmic contact between the source layer 51 and the epitaxial layer 20 and the ohmic contact between the drain layer 52 and the epitaxial layer 20 .
  • the material of the doped layer 30 can also be other materials, and the thickness of the doped layer 30 can also be in other thickness ranges, which are not limited in the embodiments of this application.
  • the thickness of doped layer 30 may be 5 nm.
  • the material of the doped layer 30 may be Si, and the state may be a polycrystalline state. That is to say, the doped layer 30 may be polycrystalline silicon.
  • the thickness of the doped layer 30 decreases from the peak concentration of silicon (which can be 80%, 70%, 60%, etc.) to the silicon concentration of 10%, which is less than 20 nm. It can be understood that when the concentration of silicon is the peak concentration, the doped layer 30 can correspond to a thickness. In the case where the silicon concentration is 10%, the doped layer 30 may correspond to another thickness. The thickness difference between the two thicknesses can be 20nm. Of course, the thickness difference between the two thicknesses will change with the concentration of silicon. The embodiment of the present application does not limit the thickness of the doped layer 30 from the peak concentration of silicon to a silicon concentration of 10%.
  • the first concentration of silicon in the doped layer 30 can also be set to 60%, and the second concentration of silicon is 10%. Then, the thickness of the doped layer 30 from the first concentration of silicon to the second concentration of silicon may be less than 20 nm.
  • the first concentration and the second concentration of silicon can also be other concentrations respectively, and the thickness of the doping layer 30 from the first concentration of silicon to the second concentration of silicon can also be in other thickness ranges, which are not covered in the embodiments of this application. limited.
  • dielectric layer 40 may include a dielectric layer. Then, the material of the dielectric layer 40 may be SiO 2 or SiN, etc., and the thickness may be 10 nm to 500 nm.
  • the dielectric layer 40 may also include two stacked dielectric layers. Then, one of the dielectric layers may be made of SiO 2 , and the other dielectric layer may be made of SiN. Alternatively, one of the dielectric layers may be made of Al 2 O 3 , and the other dielectric layer may be made of SiN. Of course, the material of the two dielectric layers can be the same, and both can be SiO 2 or SiN. The thickness of the two dielectric layers can be 5 nm to 500 nm respectively. The relative dielectric constant of the dielectric layer 40 can be increased, thereby improving the insulation of the dielectric layer 40 , reducing the quiescent current of the semiconductor device 1 , and reducing the quiescent power consumption of the semiconductor device 1 . Of course, the material of the dielectric layer 40 can also be other materials, and the thickness can also be in other thickness ranges, which are not limited in the embodiments of this application.
  • the bottom of the above-mentioned groove A may be located at the cap layer 23 , the barrier layer 22 or the channel layer 21 .
  • the location of groove A can be introduced with reference to Figures 2 to 7 below. It should be noted that, in order to clearly describe the position of the bottom of the groove A, the electrode layer 50 is not shown in the above-mentioned FIGS. 2 to 7 .
  • the position of the bottom of groove A can be divided into the following situations:
  • Case 1 The bottom of the groove A may be located inside the capping layer 23, as shown in Figure 2.
  • the bottom of groove A is located on the capping layer 23 close to the surface of the dielectric layer 40, as shown in FIG. 3 . That is, the bottom of the groove A may be located inside or on the upper surface of the capping layer 23 .
  • the doped layer 30 and the capping layer 23 can react chemically to form an N-type doped (such as silicon doped) region.
  • the electrode layer 50 reacts chemically with the N-type doped region to form an ohmic contact with low resistivity. That is to say, ohmic contact between the electrode layer 50 and the cap layer 23 is achieved, and the contact resistivity of the ohmic contact is reduced through the doping layer 30 .
  • Case 2 The bottom of the groove A may be located inside the barrier layer 22 , as shown in FIG. 4 .
  • the bottom of the groove A may be located on the surface of the barrier layer 22 close to the capping layer 21, as shown in FIG. 5 . That is, the bottom of the groove A may be located inside or on the upper surface of the barrier layer 22 .
  • the doping layer 30 and the barrier layer 22 can react chemically to form an N-type doped (eg silicon doped) region.
  • the electrode layer 50 reacts chemically with the N-type doped region to form an ohmic contact with low resistivity. That is to say, ohmic contact between the electrode layer 50 and the barrier layer 22 is achieved, and the contact resistivity of the ohmic contact is reduced through the doping layer 30 .
  • Case 3 The bottom of the groove A may be located inside the channel layer 21, as shown in FIG. 6 .
  • the bottom of the groove A may be located on a surface of the channel layer 21 close to the barrier layer 22, as shown in FIG. 7 . That is, the bottom of the groove A may be located inside or on the upper surface of the channel layer 21 .
  • a chemical reaction can occur between the doped layer 30 and the channel layer 21 to form an N-type doped (such as silicon doped) region.
  • the electrode layer 50 reacts chemically with the N-type doped region to form an ohmic contact with low resistivity. That is to say, ohmic contact between the electrode layer 50 and the channel layer 21 is achieved, and the contact resistivity of the ohmic contact is reduced through the doping layer 30 .
  • the distance between the bottom of the groove A and the upper surface of the channel layer 21 is within 10 nm. Then, you can have the following two structures:
  • the bottom of the groove A can be located inside the barrier layer 22 and within a distance of 10 nm from the upper surface of the channel layer 21 , as shown in FIG. 1 .
  • the bottom of the groove A can be located inside the channel layer 21 and within a distance of 10 nm from the upper surface of the channel layer 21, as shown in Figure 8.
  • the above two structures can also realize ohmic contact between the electrode layer 50 and the barrier layer 22 , or realize ohmic contact between the electrode layer 50 and the channel layer 21 , and can minimize the contact resistivity of the ohmic contact.
  • the contact resistivity can be reduced to 0.5 ⁇ mm, which not only improves the working efficiency of the semiconductor device 1, but also reduces the preparation cost of the semiconductor device 1.
  • the semiconductor device 1 provided in the embodiment of the present application can be a field effect transistor, and further can be a high electron mobility transistor (HEMT) or a heterojunction field effect transistor (HFET). Or modulation-doped FET (MODFET).
  • HEMT high electron mobility transistor
  • HFET heterojunction field effect transistor
  • MODFET modulation-doped FET
  • the semiconductor device 1 can also be other types of transistors, which are not limited in the embodiments of this application.
  • the embodiment of the present application provides a method for preparing a semiconductor device 1. As shown in Figure 9, the preparation process 100 can be implemented according to the following steps:
  • Step S101 Perform photolithography on the epitaxial layer 20 to form a mask layer 70, as shown in FIG. 10 .
  • step S101 photolithography is performed on the epitaxial layer 20 to form the mask layer 70 , which can be further implemented as follows:
  • Step S101a1 Coat photoresist on the surface of the epitaxial layer 20 (which may be the capping layer 23 of the epitaxial layer 20), and bake the epitaxial layer 20 coated with photoresist according to the preset baking temperature and preset baking time.
  • the preset baking temperature may be 90°C to 120°C.
  • the preset baking time can be 60 to 120 seconds to solidify the liquid photoresist on the surface of the epitaxial layer 20 .
  • the preset baking temperature can also be in other temperature ranges, and the preset baking time can also be in other time ranges, which are not limited in the embodiments of this application.
  • photoresist is coated on the surface of the epitaxial layer 20, and the epitaxial layer 20 coated with the photoresist is baked for 90 seconds at a baking temperature of 90°C.
  • the photoresist may be Az5214 type photoresist.
  • the photoresist can also be of other types, which is not limited in the embodiments of this application.
  • Step S101a2 Expose the baked epitaxial layer 20 according to the preset exposure time.
  • the preset exposure time can be 100ms to 1000ms, which can transfer the pattern on the mask to the cured photoresist.
  • the preset exposure time can also be in other time ranges, which is not limited in the embodiments of this application.
  • the baked epitaxial layer 20 is exposed for 200 ms.
  • Step S101a3 Use a developer to develop the exposed epitaxial layer 20 according to a preset development time to form a mask layer 70.
  • the developer may be a tetramethylammonium hydroxide (TMAH) solution (which may be referred to as a TMAH solution).
  • TMAH tetramethylammonium hydroxide
  • the developer can also be other solutions, which are not limited in the embodiments of this application.
  • the preset development time may be 30 to 90 s, and the pattern on the cured photoresist may be transferred to the epitaxial layer 20 .
  • a TMAH solution can be used to develop the exposed epitaxial layer 20 for 50 seconds to form a mask layer 70 with a thickness of 1 ⁇ m.
  • the preparation process 100 may also include:
  • Step S102 Forming the doping layer 30 according to the mask layer 70, which can be divided into the following embodiments for introduction:
  • the doped layer 30 is formed according to the following steps:
  • Step S102a1 Etch part of the epitaxial layer 20 according to the mask layer 70 of FIG. 10 to form a groove A, as shown in FIG. 13.
  • a dry etching process or a wet etching process may be used to etch part of the epitaxial layer 20 for 5 to 100 minutes.
  • the dry etching process can include reactive ion etching (RIE) process (RIE process for short), inductively coupled plasma etching (ICP process for short), ion etching (ICP process for short), Any one of the ion beam etching (IBE) process (referred to as the IBE process) and the advanced oxide etch (AOE) process (referred to as the AOE process).
  • RIE reactive ion etching
  • ICP process inductively coupled plasma etching
  • ICP process ion etching
  • AOE advanced oxide etch
  • the ICP process can be used to etch part of the epitaxial layer 20 for 10 minutes, and the part of the epitaxial layer 20 is physically bombarded by the inductively coupled plasma. At the same time, a chemical reaction occurs between the inductively coupled plasma and the epitaxial layer 20 to achieve dual effects. Etching, the etching rate is fast.
  • Step S102a2 Plasma can be used to process the groove A according to the preset processing time.
  • Ar can be used to treat groove A for 10 minutes, which can not only increase the surface roughness of groove A, but also increase the N vacancies on the surface of groove A, further reducing the ohmic resistance of the electrode layer 50 and the epitaxial layer 20 Contact resistivity of the contact.
  • Step S102a3 Use a deposition process to form the doping layer 30 inside the groove A, as shown in Figures 14 and 15.
  • the material, state and thickness of the doping layer 30 can be referred to the above introduction, and will not be described again in the embodiment of the present application.
  • the deposition process may include an atomic layer deposition (ALD) process (ALD process for short), plasma enhanced atomic layer deposition (PEALD) process (PEALD process for short), plasma Volume enhanced chemical vapor deposition (plasma enhanced chemical vapor deposition, PECVD) process (referred to as PECVD process), inductively coupled plasma chemical vapor deposition (inductively coupled plasma chemical vapor deposition, ICPCVD) process (referred to as ICPCVD process), low pressure chemical vapor deposition Any one of the deposition (low pressure chemical vapor deposition, LPCVD) process (referred to as the LPCVD process), the electron beam evaporation (electronic beam evaporation, EBE) process (referred to as the EBE process) and the sputter deposition process.
  • ALD atomic layer deposition
  • PEALD plasma enhanced atomic layer deposition
  • PECVD plasma Volume enhanced chemical vapor deposition
  • ICPCVD inductively coupled plasma chemical vapor deposition
  • ICPCVD inductively
  • a PECVD process is used to deposit polysilicon inside the groove A to form a doped layer 30 with a thickness of 5 nm.
  • the doped layer 30 is formed according to the following steps:
  • Step S102b1 Use plasma to process the surface of the epitaxial layer 20 in Figure 10 according to the preset processing time, as shown in Figure 17. That is to say, after obtaining the structure shown in FIG. 10 , the epitaxial layer 20 may not be etched, but the surface of the epitaxial layer 20 may be directly processed.
  • Step S102b2 According to the mask layer 70, form the doped layer 30 on the surface of the epitaxial layer 20 (which may be the cap layer 23), as shown in FIG. 18.
  • part of the epitaxial layer 20 is etched according to the mask layer 70 to form the groove A, and the groove A is processed to further form the doping layer 30 inside the groove A.
  • part of the epitaxial layer 20 is not etched, but the surface of the epitaxial layer 20 is directly processed, and the doping layer 30 is formed on the surface of the epitaxial layer 20 according to the mask layer 70 .
  • Step S103 Form an electrode layer 50 on the surface of the doped layer 30, and anneal the electrode layer 50 according to a preset annealing temperature.
  • an electrode layer 50 (including a source layer 51 and a drain layer 52 ) can be formed on the surface of the doped layer 30 in FIG. 15 .
  • Mask layer 70 is removed, as shown in Figure 20. Annealing the electrode layer 50 according to the preset annealing temperature can not only achieve ohmic contact between the electrode layer 50 and the epitaxial layer 20 , but also reduce the contact resistivity of the ohmic contact through the doping layer 30 .
  • the electrode layer 50 (including the source electrode) can be formed on the surface of the doped layer 30 in FIG. 18 layer 51 and drain layer 52).
  • Mask layer 70 is removed, as shown in Figure 21. Annealing the electrode layer 50 according to the preset annealing temperature can also achieve ohmic contact between the electrode layer 50 and the epitaxial layer 20 , and the contact resistivity of the ohmic contact can be reduced through the doping layer 30 .
  • the material, state and thickness of the doping layer 30 can be referred to the above introduction, and will not be described again in the embodiment of the present application.
  • the source layer 51 and the drain layer 52 can be annealed using annealing equipment such as an annealing furnace or laser at a preset annealing temperature of 400°C to 800°C.
  • annealing equipment such as an annealing furnace or laser at a preset annealing temperature of 400°C to 800°C.
  • the performance requirements for the annealing equipment are low and the implementation is relatively low.
  • Temperature annealing not only reduces the annealing cost, but is also compatible with the subsequent preparation process of the gate layer 60 .
  • the above two possible implementation methods can use any one of the above deposition processes to deposit metal on the surface of the cap layer 23, and remove the metal on the surface of the mask layer 70 through a stripping process or a dry etching process.
  • Source layer 51 and drain layer 52 are formed.
  • the stripping process refers to that after the capping layer 23 is coated with photoresist, exposed, and developed, the deposited metal is evaporated using a photoresist with a certain pattern as a mask, and then the photoresist is removed. At the same time, the metal deposited on the mask is peeled off to form the source layer 51 and the drain layer 52 .
  • the dry etching process refers to the use of reactive gases and plasma to etch deposited metal. In this embodiment of the present application, a reactive ion etching process may be used to remove metal on the surface of the mask layer 70 to form the source layer 51 and the drain layer 52 .
  • the EBE process is used to sequentially deposit Ti, Al, Ti, and Au on the surface of the doped layer 30 to form the source layer 51 and the drain layer 52 .
  • the thicknesses of Ti, Al, Ti, and Au correspond to 20nm, 150nm, 30nm, and 50nm.
  • the gate layer 60 can also be formed through the following steps:
  • Step S104a1 Form the dielectric layer 40 on the surface of the epitaxial layer 20 (which may be the cap layer 23).
  • the dielectric layer 40 can be formed on the basis of what is shown in Figure 20, as shown in Figure 23; or the dielectric layer 40 can also be formed on the basis of what is shown in Figure 21, which will not be described again here.
  • Step S104a2 Perform photolithography and etching on the dielectric layer 40 to form the groove B.
  • a groove B is formed, as shown in FIG. 24.
  • Step S104a3 Form the gate layer 60 inside the groove B.
  • the gate layer 60 is formed on the basis shown in FIG. 24 , as shown in FIG. 1 .
  • the method for manufacturing the semiconductor device 1 provided by the embodiment of the present application can be implemented through FIG. 25 or FIG. 26 , and the steps are described in detail below.
  • the preparation process 200 can be implemented through the following steps:
  • Step S201 Perform photolithography on the epitaxial layer 20 to form a mask layer 70, as shown in FIG. 10 .
  • Step S202 Etch part of the epitaxial layer 20 according to the mask layer 70 to form a groove A, as shown in FIG. 13 .
  • Step S203 Use plasma to process groove A, as shown in Figure 14.
  • Step S204 Form the doping layer 30 inside the groove A, as shown in FIG. 15 .
  • Step S205 Form an electrode layer 50 on the surface of the doped layer 30, as shown in Figure 19.
  • Step S206 Remove the mask layer 70, as shown in Figure 20.
  • Step S207 Anneal the electrode layer 50 according to the preset annealing temperature.
  • Step S208 Form a dielectric layer 40 on the surface of the epitaxial layer 20, as shown in FIG. 23.
  • Step S209 Perform photolithography and etching on the dielectric layer 40 to form groove B.
  • Step S210 Form the gate layer 60 inside the groove B, as shown in FIG. 1 .
  • step S201 can be referred to the above introduction, and will not be described again in the embodiment of the present application.
  • the preparation process 300 can be implemented through the following steps:
  • Step S301 Perform photolithography on the epitaxial layer 20 to form a mask layer 70, as shown in FIG. 10 .
  • Step S302 Use plasma to process the epitaxial layer 20, as shown in Figure 17.
  • Step S303 According to the mask layer 70, form the doping layer 30 on the surface of the epitaxial layer 20, as shown in FIG. 18.
  • Step S304 Form the electrode layer 50 on the surface of the doped layer 70.
  • Step S305 Remove the mask layer 70, as shown in Figure 21.
  • Step S306 Anneal the electrode layer 50 according to the preset annealing temperature.
  • Step S307 Form the dielectric layer 40 on the surface of the epitaxial layer 20.
  • Step S308 Perform photolithography and etching on the dielectric layer 40 to form the groove B.
  • Step S309 Form the gate layer 60 inside the groove B.
  • step S301 to step S309 can be referred to the above introduction, and will not be described again in the embodiment of the present application.
  • the preparation process 200 part of the epitaxial layer 20 is etched, and then the doped layer 30, the electrode layer 50, the dielectric layer 40 and the gate layer 60 are formed.
  • the preparation process 300 only the epitaxial layer 20 is photolithographed, and then the doping layer 30 , the electrode layer 50 , the dielectric layer 40 and the gate layer 60 are formed.
  • the embodiment of the present application provides another method of preparing a semiconductor device 1.
  • the preparation process 400 can be implemented according to the following steps:
  • Step S401 Perform photolithography on the dielectric layer 40 to form a mask layer 70.
  • the dielectric layer 40 may be formed on the surface of the epitaxial layer 20, as shown in FIG. 28.
  • step S101 photolithography is performed on the dielectric layer 40 to form the mask layer 70 (as shown in Figure 30), which can be further implemented as follows:
  • Step S401a1 Coat photoresist on the surface of the dielectric layer 40, and bake the dielectric layer 40 coated with photoresist according to the preset baking temperature and preset baking time.
  • the dielectric layer 40 coated with photoresist can be baked at a preset baking temperature of 90°C to 120°C and a preset baking time of 60s to 120s, so that the liquid photoresist is on the surface of the dielectric layer 40 solidify.
  • the dielectric layer 40 coated with photoresist can also be baked at other baking temperatures and other baking times, which are not limited by the embodiments of the present application.
  • photoresist Az5214 can be coated on the surface of the dielectric layer 40, and the dielectric layer 40 coated with the photoresist is baked at a baking temperature of 90°C for 90 seconds.
  • Step S401a2 Expose the baked dielectric layer 40 according to the preset exposure time.
  • the baked dielectric layer 40 can be exposed with a preset exposure time of 100 ms to 1000 ms, so that the pattern on the mask can be transferred to the cured photoresist.
  • the preset exposure time can also be in other time ranges, which is not limited in the embodiments of this application.
  • the baked dielectric layer 40 may be exposed for 200 ms.
  • Step S401a3 Use a developer to develop the exposed dielectric layer 40 according to a preset development time to form a mask layer 70, as shown in FIG. 30 .
  • a TMAH solution can be used to develop the exposed dielectric layer 40 with a preset development time of 30 to 90 seconds, and the pattern on the cured photoresist can be transferred to the dielectric layer 40 .
  • the developing solution can also be other solutions, and the preset development time can also be other time ranges, which are not limited in the embodiments of this application.
  • a TMAH solution can be used to develop the exposed dielectric layer 40 for 50 seconds to form a mask layer 70 with a thickness of 1 ⁇ m.
  • Step S402 Forming the doping layer 30 according to the mask layer 70, which can be divided into the following embodiments for introduction:
  • the doped layer 30 may be formed according to the following steps:
  • Step S402a1 Etch the dielectric layer 40 and part of the epitaxial layer 20 according to the mask layer 70 in Figure 30 to form a groove A, as shown in Figure 31 .
  • Step S402a2 Remove the mask layer 70, as shown in Figure 32.
  • Step S402a3 Use plasma to process groove A according to the preset processing time, as shown in Figure 33.
  • Ar can be used to treat groove A for 10 minutes, which can not only increase the surface roughness of groove A, but also increase the N vacancies on the surface of groove A, further reducing the ohmic resistance of the electrode layer 50 and the epitaxial layer 20 Contact resistivity of the contact.
  • Step S402a4 Use a deposition process to form the doping layer 30 inside the groove A, as shown in Figure 34.
  • the material, state, thickness and deposition process of the doping layer 30 can be referred to the above introduction, and will not be described again in the embodiment of the present application.
  • a PECVD process is used to deposit polysilicon inside the groove A to form a doped layer 30 with a thickness of 5 nm.
  • the doping layer 30 may be formed according to the following steps:
  • Step S402b1 Etch the dielectric layer 40 according to the mask layer 70 in Figure 30 to form a groove A, as shown in Figure 35 .
  • Step S402b2 Remove the mask layer 70.
  • Step S402b3 Use plasma to process groove A according to the preset processing time.
  • Ar can be used to treat groove A for 10 minutes, which can not only increase the surface roughness of groove A, but also increase the N vacancies on the surface of groove A, further reducing the ohmic resistance of the electrode layer 50 and the epitaxial layer 20 Contact resistivity of the contact.
  • Step S402b4 Use a deposition process to form the doping layer 30 inside the groove A, as shown in Figure 36.
  • the material, state, thickness and deposition process of the doping layer 30 can be referred to the above introduction, and will not be described again in the embodiment of the present application.
  • a PECVD process is used to deposit polysilicon inside the groove A to form a doped layer 30 with a thickness of 5 nm.
  • step S402a1 to step S402a4 the dielectric layer 40 and part of the epitaxial layer 20 are etched according to the mask layer 70 to form the groove A, the groove A is processed, and further inside the groove A Doped layer 30 is formed.
  • steps S402b1 to S402b4 only the dielectric layer 40 is etched according to the mask layer 70 to form the groove A, the groove A is processed, and the doping layer 30 is further formed inside the groove A.
  • Step S403 Form an electrode layer 50 on the surface of the doped layer 30, and anneal the electrode layer 50 according to a preset annealing temperature.
  • the electrode layer 50 (that is, the source layer 51 and the drain layer 52 are formed) can be formed on the surface of the doped layer 30 in FIG. 34 , as shown in FIG. 23 .
  • Annealing the electrode layer 50 according to the preset annealing temperature can not only achieve ohmic contact between the electrode layer 50 and the epitaxial layer 20 , but also reduce the contact resistivity of the ohmic contact through the doping layer 30 .
  • the electrode layer 50 (that is, the source layer 51 and the drain layer 52 are formed) can be formed on the surface of the doped layer 30 in FIG. 36 .
  • Annealing the electrode layer 50 according to the preset annealing temperature can also achieve ohmic contact between the electrode layer 50 and the epitaxial layer 20 , and the contact resistivity of the ohmic contact can be reduced through the doping layer 30 .
  • the material, state and thickness of the doping layer 30 can be referred to the above introduction, and will not be described again in the embodiment of the present application.
  • the source layer 51 and the drain layer 52 can be annealed using annealing equipment such as an annealing furnace or laser at a preset annealing temperature of 400°C to 800°C.
  • annealing equipment such as an annealing furnace or laser at a preset annealing temperature of 400°C to 800°C.
  • the performance requirements for the annealing equipment are low and the implementation is relatively low.
  • Temperature annealing not only reduces the annealing cost, but is also compatible with the subsequent preparation process of the gate layer 60 .
  • the above two possible implementation methods can use any one of the above deposition processes to deposit metal on the surface of the cap layer 23, and remove the metal on the surface of the mask layer 70 through a stripping process or an etching process to form a source. electrode layer 51 and drain layer 52.
  • the EBE process is used to sequentially deposit Ti, Al, Ti, and Au on the surface of the doped layer 30 to form the source layer 51 and the drain layer 52 .
  • the thicknesses of Ti, Al, Ti, and Au correspond to 20nm, 150nm, 30nm, and 50nm.
  • the gate layer 60 can also be formed through the following steps:
  • Step S404a1 Perform photolithography and etching on the dielectric layer 40 to form groove B.
  • groove B is formed on the basis shown in Fig. 23, as shown in Fig. 24.
  • Step S404a2 Form the gate layer 60 inside the groove B.
  • the gate layer 60 is formed on the basis shown in FIG. 24 , as shown in FIG. 1 .
  • the method for manufacturing the semiconductor device 1 provided by the embodiment of the present application can be implemented through FIG. 37 , and the steps are described in detail below.
  • the preparation process 500 can be implemented through the following steps:
  • Step S501 Form a dielectric layer 40 on the surface of the epitaxial layer 20, as shown in Figure 28.
  • Step S502 Perform photolithography on the dielectric layer 40 to form a mask layer 70, as shown in FIG. 30 .
  • Step S503 Etch the dielectric layer 40 and part of the epitaxial layer 20 according to the mask layer 70 to form a groove A.
  • the dielectric layer 40 is etched according to the mask layer 70 to form the groove A.
  • the groove A formed is as shown in FIG. 31 . If the dielectric layer 40 is etched, the groove A formed is as shown in FIG. 35 .
  • Step S504 Remove the mask layer 70, as shown in Figure 32.
  • Step S505 Use plasma to process groove A, as shown in Figure 33.
  • Step S506 Form the doping layer 30 inside the groove A, as shown in Figure 34 or Figure 36.
  • Step S507 Form an electrode layer 50 on the surface of the doped layer 30, as shown in FIG. 23.
  • Step S508 Anneal the electrode layer 50 according to the preset annealing temperature.
  • Step S509 Perform photolithography and etching on the dielectric layer 40 to form groove B.
  • Step S510 Form the gate layer 60 inside the groove B, as shown in FIG. 1 .
  • step S501 to step S510 can be referred to the above introduction, and will not be repeated in the embodiment of this application. narrate.
  • the size of the sequence numbers of the above-mentioned processes does not mean the order of execution.
  • the execution order of each process should be determined by its functions and internal logic, and should not be used in the embodiments of the present application.
  • the implementation process constitutes any limitation.
  • the embodiment of the present application provides an electronic chip, which may include passive devices and semiconductor devices 1 .
  • the passive device may be electrically connected to the semiconductor device 1 .
  • passive components may be resistors, capacitors, etc.
  • the passive components can also be other components, which are not limited in the embodiments of this application.
  • An embodiment of the present application provides an electronic device, which may include a circuit board and the above-mentioned electronic chip.
  • the electronic chip can be arranged on the circuit board.

Landscapes

  • Engineering & Computer Science (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Power Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Computer Hardware Design (AREA)
  • Ceramic Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Electrodes Of Semiconductors (AREA)

Abstract

Provided in the present application are a semiconductor device and a preparation method therefor, which realize ohmic contact between a first electrode layer and an epitaxial layer, reduce the contact resistivity of ohmic contact, are conducive to reducing the on-resistance of the semiconductor device, and thus decrease the power loss of the semiconductor device. The semiconductor device may comprise an epitaxial layer, a doped layer, a dielectric layer and a first electrode layer, wherein the epitaxial layer and the dielectric layer are stacked. The semiconductor device is provided with a first recess, wherein one part of the doped layer and one part of the first electrode layer can be stacked inside the first recess.

Description

半导体器件及其制备方法Semiconductor device and preparation method thereof
本申请要求于2022年09月13日提交中国专利局、申请号为202211107921.9、申请名称为“半导体器件及其制备方法”的中国专利申请的优先权,其全部内容通过引用结合在本申请中。This application claims priority to the Chinese patent application filed with the China Patent Office on September 13, 2022, with the application number 202211107921.9 and the application title "Semiconductor Device and Preparation Method thereof", the entire content of which is incorporated into this application by reference.
技术领域Technical field
本申请涉及半导体技术领域,并且更具体地,涉及一种半导体器件及其制备方法。The present application relates to the field of semiconductor technology, and more specifically, to a semiconductor device and a manufacturing method thereof.
背景技术Background technique
随着科技的飞速发展,半导体器件(如高电子迁移率晶体管等)在手机、平板电脑等电子设备中得到了广泛的应用。相关技术提供的半导体器件往往通过电极层(如源极层和漏极层)的金属种类与配比、外延层的厚度等形成电极层与外延层的欧姆接触。但是,欧姆接触的电阻率较高,通常会大于1Ω·mm,不利于减小半导体器件的导通电阻。With the rapid development of science and technology, semiconductor devices (such as high electron mobility transistors, etc.) have been widely used in electronic devices such as mobile phones and tablet computers. Semiconductor devices provided by related technologies often form ohmic contact between the electrode layer and the epitaxial layer through the metal type and ratio of the electrode layer (such as the source layer and the drain layer), the thickness of the epitaxial layer, etc. However, the resistivity of ohmic contact is high, usually greater than 1Ω·mm, which is not conducive to reducing the on-resistance of semiconductor devices.
因此,如何减小欧姆接触的接触电阻率成了亟需解决的技术问题。Therefore, how to reduce the contact resistivity of ohmic contact has become an urgent technical problem that needs to be solved.
发明内容Contents of the invention
本申请提供了一种半导体器件及其制备方法,实现了第一电极层与外延层的欧姆接触,减小了欧姆接触的接触电阻率,有助于减小半导体器件的导通电阻,进而降低半导体器件的功率损耗。The present application provides a semiconductor device and a preparation method thereof, which realizes ohmic contact between the first electrode layer and the epitaxial layer, reduces the contact resistivity of the ohmic contact, helps to reduce the on-resistance of the semiconductor device, and thereby reduces Power losses in semiconductor devices.
第一方面,本申请提供了一种半导体器件,可以包括外延层、掺杂层、介质层和第一电极层。其中,外延层和介质层可以层叠设置。半导体器件可以设有第一凹槽,掺杂层和第一电极层的一部分可以层叠设置于第一凹槽内部。可以理解的,第一电极的一部分设置于第一凹槽内部,第一电极的另一部分可以设置于第一凹槽外部。In a first aspect, the present application provides a semiconductor device, which may include an epitaxial layer, a doping layer, a dielectric layer and a first electrode layer. Wherein, the epitaxial layer and the dielectric layer can be stacked. The semiconductor device may be provided with a first groove, and a part of the doping layer and the first electrode layer may be stacked inside the first groove. It can be understood that a part of the first electrode may be disposed inside the first groove, and another part of the first electrode may be disposed outside the first groove.
本申请提供的半导体器件通过掺杂层形成第一电极层与外延层的欧姆接触,减小了欧姆接触的接触电阻率,有助于减小半导体器件的导通电阻,进而降低半导体器件的功率损耗。The semiconductor device provided by this application forms the ohmic contact between the first electrode layer and the epitaxial layer through the doping layer, which reduces the contact resistivity of the ohmic contact, helps to reduce the on-resistance of the semiconductor device, and thereby reduces the power of the semiconductor device. loss.
在一种可能的实现方式中,掺杂层、外延层和第一电极层均不同。也就是说,掺杂层与外延层之间存在明确的界限。掺杂层与第一电极层之间也存在明确的界限。In a possible implementation, the doped layer, the epitaxial layer and the first electrode layer are all different, that is, there is a clear boundary between the doped layer and the epitaxial layer, and there is also a clear boundary between the doped layer and the first electrode layer.
在另一种可能的实现方式中,掺杂层的材料可以为硅、氧化硅、氮化硅和氮氧化硅中的任意一种或多种。掺杂层的状态可以为单晶状态、多晶状态或非晶状态。掺杂层的厚度可以为1nm~50nm。通过掺杂层可以实现第一电极层与外延层的欧姆接触。当然,掺杂层的材料还可以为其他材料,掺杂层的厚度还可以为其他厚度范围,本申请不做限定。In another possible implementation, the material of the doping layer may be any one or more of silicon, silicon oxide, silicon nitride, and silicon oxynitride. The state of the doped layer may be a single crystal state, a polycrystalline state or an amorphous state. The thickness of the doped layer may be 1 nm to 50 nm. Ohmic contact between the first electrode layer and the epitaxial layer can be achieved through the doping layer. Of course, the material of the doped layer can also be other materials, and the thickness of the doped layer can also be in other thickness ranges, which is not limited in this application.
在一示例中,掺杂层从硅的峰值浓度降到硅浓度为10%的厚度可以小于20nm。其中,硅的峰值浓度可以为80%、70%、60%等。可以理解的,硅的浓度为峰值浓度的情况下,掺杂层可以对应一个厚度。硅的浓度为10%的情况下,掺杂层可以对应另一个厚度。两个厚度之间的厚度差可以小于20nm,能够减小第一电极层与外延层之间欧姆接触的接触电阻率。当然,两个厚度之间的厚度差会随着硅的浓度而改变,本申请对掺杂层从硅的峰值浓度降到硅浓度为10%的厚度不做限定。In one example, the thickness of the doped layer from a peak concentration of silicon down to a silicon concentration of 10% may be less than 20 nm. Among them, the peak concentration of silicon can be 80%, 70%, 60%, etc. It can be understood that when the concentration of silicon is the peak concentration, the doped layer can correspond to a thickness. In the case of a silicon concentration of 10%, the doped layer can correspond to another thickness. The thickness difference between the two thicknesses may be less than 20 nm, which can reduce the contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer. Of course, the thickness difference between the two thicknesses will change with the concentration of silicon. This application does not limit the thickness of the doped layer from the peak concentration of silicon to a silicon concentration of 10%.
在另一示例中,掺杂层从硅的第一浓度降到硅浓度为10%的厚度可以小于20nm。其中,第一浓度可以大于或等于60%。例如,第一浓度可以为70%或60%等。可以理解的,在硅的第一浓度的情况下,掺杂层可以对应一个厚度。在硅浓度为10%的情况下,掺杂层可以对应另一个厚度。两个厚度之间的厚度差可以小于20nm,能够减小第一电极层与外延层之间欧姆接触的接触电阻率。当然,两个厚度之间的厚度差会随着硅的浓度而改变,本申请对掺杂层从硅的第一浓度降到硅的第二浓度的厚度不做限定。In another example, the thickness of the doped layer from a first concentration of silicon to a silicon concentration of 10% may be less than 20 nm. Wherein, the first concentration may be greater than or equal to 60%. For example, the first concentration may be 70% or 60%, etc. It can be understood that in the case of the first concentration of silicon, the doped layer may correspond to a thickness. In the case of a silicon concentration of 10%, the doped layer can correspond to another thickness. The thickness difference between the two thicknesses may be less than 20 nm, which can reduce the contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer. Of course, the thickness difference between the two thicknesses will change with the concentration of silicon. This application does not limit the thickness of the doped layer from the first concentration of silicon to the second concentration of silicon.
在一种可能的实现方式中,外延层可以包括层叠设置于衬底表面的沟道层、势垒层和盖帽层。也就是说,衬底、沟道层、势垒层和盖帽层依次层叠设置。In a possible implementation, the epitaxial layer may include a channel layer, a barrier layer and a cap layer that are stacked on the surface of the substrate. That is to say, the substrate, channel layer, barrier layer and cap layer are stacked in sequence.
可选地,第一凹槽的底部可以位于盖帽层、势垒层或沟道层。也就是说,第一凹槽的底部可以位于盖帽层的表面或内部、势垒层的表面或内部,还可以位于沟道层的内部。进而能够使第一电极层与 盖帽层、势垒层或沟道层形成欧姆接触。Alternatively, the bottom of the first groove may be located at the cap layer, barrier layer or channel layer. That is to say, the bottom of the first groove can be located on the surface or inside the cap layer, on the surface or inside the barrier layer, or can also be located inside the channel layer. Furthermore, it is possible to make the first electrode layer and The cap layer, barrier layer or channel layer forms an ohmic contact.
进一步地,第一凹槽的底部与沟道层的表面可以距离20nm以内。沟道层与势垒层之间可以具有明确的边界,可以将沟道层厚度的边界看作为沟道层的表面。沟道层的表面可以用于指示沟道层靠近势垒层的表面。Further, the distance between the bottom of the first groove and the surface of the channel layer may be within 20 nm. There may be a clear boundary between the channel layer and the barrier layer, and the boundary of the thickness of the channel layer may be regarded as the surface of the channel layer. The surface of the channel layer may be used to indicate the surface of the channel layer close to the barrier layer.
可以看出,第一凹槽的底部可以位于势垒层内部,或者位于沟道层内部。不管第一凹槽的底部位于第一凹槽的底部还是势垒层内部,第一凹槽的底部距离沟道层的表面的距离都可以在20nm以内。可以实现第一电极层与势垒层的欧姆接触,或者实现第一电极层与沟道层的欧姆接触,且可以最大程度的降低欧姆接触的接触电阻率,可以将接触电阻率降低到0.5Ω·mm,提高半导体器件的工作效率的同时,能够降低半导体器件的制备成本。It can be seen that the bottom of the first groove may be located inside the barrier layer or inside the channel layer. Regardless of whether the bottom of the first groove is located at the bottom of the first groove or inside the barrier layer, the distance between the bottom of the first groove and the surface of the channel layer can be within 20 nm. The ohmic contact between the first electrode layer and the barrier layer can be realized, or the ohmic contact between the first electrode layer and the channel layer can be realized, and the contact resistivity of the ohmic contact can be reduced to the greatest extent, and the contact resistivity can be reduced to 0.5Ω. ·mm, while improving the working efficiency of semiconductor devices, it can also reduce the preparation cost of semiconductor devices.
在另一种可能的实现方式中,介质层可以设有第二凹槽,第二凹槽的底部可以位盖帽层的表面,其中,盖帽层的表面可以用于指示盖帽层背离势垒层的表面。半导体器件还可以包括第二电极层,第二电极层可以位于第二凹槽内部,第二电极层与盖帽层可以形成肖特基接触。In another possible implementation, the dielectric layer may be provided with a second groove, and the bottom of the second groove may be located on the surface of the capping layer, wherein the surface of the capping layer may be used to indicate that the capping layer is away from the barrier layer. surface. The semiconductor device may further include a second electrode layer, the second electrode layer may be located inside the second groove, and the second electrode layer and the cap layer may form a Schottky contact.
示例性的,第二电极层可以为栅极层,因此,栅极层可以与盖帽层可以形成肖特基接触。For example, the second electrode layer may be a gate layer. Therefore, the gate layer and the cap layer may form a Schottky contact.
在一种可能的实现方式中,第一电极层的材料可以包括钛Ti、金Au和铝Al中的任意一种或多种。In a possible implementation, the material of the first electrode layer may include any one or more of titanium Ti, gold Au, and aluminum Al.
由于第一电极层可以包括源极层和漏极层,因此,源极层的材料可以包括钛Ti、金Au和铝Al中的任意一种或多种。漏极层的材料也可以包括钛Ti、金Au和铝Al中的任意一种或多种。当然,源极层和漏极层的材料还可以为其他类型,本申请不做限定。Since the first electrode layer may include a source layer and a drain layer, the material of the source layer may include any one or more of titanium Ti, gold Au, and aluminum Al. The material of the drain layer may also include any one or more of titanium Ti, gold Au, and aluminum Al. Of course, the materials of the source layer and the drain layer can also be of other types, which are not limited in this application.
在另一种可能的实现方式中,第二电极层的材料可以包括钛Ti、金Au和镍Ni中的任意一种或多种。当然,第二电极层的材料还可以为其他类型,本申请不做限定。In another possible implementation, the material of the second electrode layer may include any one or more of titanium Ti, gold Au, and nickel Ni. Of course, the material of the second electrode layer can also be of other types, which is not limited in this application.
第二方面,本申请提供了一种半导体器件的制备方法,可以用于制备上述第一方面及其可能的实现方式提供的半导体器件。制备方法可以包括:对外延层进行光刻,形成掩膜层。根据掩膜层形成掺杂层。在掺杂层的表面形成第一电极层,按照预设退火温度对第一电极层进行退火。其中,预设退火温度可以为400℃~800℃。In a second aspect, the present application provides a method for manufacturing a semiconductor device, which can be used to prepare the semiconductor device provided by the first aspect and its possible implementations. The preparation method may include: performing photolithography on the epitaxial layer to form a mask layer. The doped layer is formed according to the mask layer. A first electrode layer is formed on the surface of the doped layer, and the first electrode layer is annealed according to a preset annealing temperature. Among them, the preset annealing temperature can be 400°C to 800°C.
本申请提供的制备方法过程简洁,制备的半导体器件中第一电极层与外延层的欧姆接触的接触电阻率大幅度减小,接触电阻率可达到0.5Ω·mm,提高半导体器件的工作效率的同时,能够降低半导体器件的制备成本。The preparation method provided by this application has a simple process. The contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer in the prepared semiconductor device is greatly reduced, and the contact resistivity can reach 0.5Ω·mm, which improves the working efficiency of the semiconductor device. At the same time, the manufacturing cost of semiconductor devices can be reduced.
在一种可能的实现方式中,对外延层进行光刻,形成掩膜层,可以包括:在外延层表面涂光刻胶,并按照预设烘烤温度和预设烘烤时间对涂有光刻胶的外延层进行烘烤。按照预设曝光时间,对烘烤后的外延层进行曝光。采用显影液,并按照预设显影时间对曝光后的外延层进行显影,形成掩膜层。In one possible implementation, photolithography of the epitaxial layer to form a mask layer may include: applying photoresist on the surface of the epitaxial layer, and applying the photoresist to the surface of the epitaxial layer according to the preset baking temperature and preset baking time. The epitaxial layer is baked. Expose the baked epitaxial layer according to the preset exposure time. Use a developing solution and develop the exposed epitaxial layer according to the preset development time to form a mask layer.
其中,预设烘烤温度可以为90℃~120℃。预设烘烤时间可以为60s~120s,能够使液态的光刻胶在外延层表面固化。当然,预设烘烤温度还可以为其他温度范围,预设烘烤时间还可以为其他时间范围,本申请不做限定。Among them, the preset baking temperature can be 90°C to 120°C. The preset baking time can be 60s to 120s, which can solidify the liquid photoresist on the surface of the epitaxial layer. Of course, the preset baking temperature can also be in other temperature ranges, and the preset baking time can also be in other time ranges, which are not limited in this application.
可选地,预设曝光时间可以为100ms~1000ms,能够将掩模版上的图形转移转移到固化后的光刻胶上。当然,预设曝光时间还可以为其他时间范围,本申请不做限定。Optionally, the preset exposure time can be 100 ms to 1000 ms, which can transfer the pattern on the mask to the cured photoresist. Of course, the preset exposure time can also be in other time ranges, which is not limited in this application.
示例性的,显影液可以为四甲基氢氧化铵(tetramethylammonium hydroxide,TMAH)溶液(可以简称为TMAH溶液)。预设显影时间可以为30s~90s,可以将固化后的光刻胶上的图形转移至外延层上。当然,显影液还可以为其他溶液,预设显影时间还可以为其他时间范围,本申请不做限定。For example, the developer may be a tetramethylammonium hydroxide (TMAH) solution (which may be referred to as a TMAH solution). The preset development time can be 30s to 90s, and the pattern on the cured photoresist can be transferred to the epitaxial layer. Of course, the developer can also be other solutions, and the preset development time can also be other time ranges, which are not limited in this application.
在另一种可能的实现方式中,根据掩膜层形成掺杂层可以包括:根据掩膜层,在外延层的表面形成掺杂层。也就是说,可以根据掩膜层在外延层的表面直接形成掺杂层。In another possible implementation, forming the doping layer according to the mask layer may include: forming the doping layer on the surface of the epitaxial layer according to the mask layer. That is to say, the doped layer can be directly formed on the surface of the epitaxial layer according to the mask layer.
进一步地,在根据掩膜层形成掺杂层之前,本申请提供的制备方法还可以包括:按照预设处理时间,采用等离子体对外延层的表面进行处理。也就是说,在光刻外延层形成掩膜层之后,可以对外延层的表面进行处理,再形成掺杂层。能够增大外延层表面的粗糙度,进一步降低第一电极层与外延层的欧姆接触的接触电阻率。Further, before forming the doping layer according to the mask layer, the preparation method provided by this application may also include: using plasma to process the surface of the epitaxial layer according to a preset processing time. That is to say, after photolithography of the epitaxial layer to form the mask layer, the surface of the epitaxial layer can be processed and then a doped layer can be formed. The surface roughness of the epitaxial layer can be increased, and the contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer can be further reduced.
其中,预设处理时间可以为2min~60min。等离子体可以包括氢气H2、氮气N2、氨气NH3、氯气Cl2、氩气Ar和氧气O2中的任意一种或多种。Among them, the preset processing time can be 2min~60min. The plasma may include any one or more of hydrogen H 2 , nitrogen N 2 , ammonia NH 3 , chlorine Cl 2 , argon Ar and oxygen O 2 .
在另一种可能的实现方式中,根据掩膜层形成掺杂层可以包括:根据掩膜层对部分外延层进行刻蚀,形成第一凹槽。采用沉积工艺在第一凹槽内部形成掺杂层。In another possible implementation, forming the doped layer according to the mask layer may include etching part of the epitaxial layer according to the mask layer to form a first groove. A deposition process is used to form a doped layer inside the first groove.
可以理解的,由于外延层可以包括层叠设置于衬底表面的沟道层、势垒层和盖帽层,那么,可以 根据掩膜层对盖帽层进行刻蚀,可以根据掩膜层对盖帽层和势垒层进行光刻,或者可以根据掩膜层对盖帽层、势垒层和沟道层进行刻蚀。于是,第一凹槽的底部可以位于盖帽层表面或内部,可以位于势垒层表面或内部,还可以位于沟道层表面或内部。It can be understood that since the epitaxial layer may include a channel layer, a barrier layer and a cap layer stacked on the surface of the substrate, then The cap layer is etched according to the mask layer, the cap layer and the barrier layer can be photolithographed according to the mask layer, or the cap layer, barrier layer and channel layer can be etched according to the mask layer. Therefore, the bottom of the first groove may be located on the surface or inside the cap layer, on the surface or inside the barrier layer, or on the surface or inside the channel layer.
可以想到的是,在第一凹槽内部形成的掺杂层也可以随着第一凹槽的底部位置的不同而处于外延层中不同的位置。It is conceivable that the doped layer formed inside the first groove may also be located at different positions in the epitaxial layer depending on the position of the bottom of the first groove.
其中,沉积工艺可以包括原子层沉积(atomic layer deposition,ALD)工艺(简称为ALD工艺)、等离子体增强原子层沉积(plasma enhanced atomic layer deposition,PEALD)工艺(简称为PEALD工艺)、等离子体增强化学气相沉积(plasma enhanced chemical vapor deposition,PECVD)工艺(简称为PECVD工艺)、电感耦合等离子体化学气相沉积(inductively coupled plasma chemical vapor deposition,ICPCVD)工艺(简称为ICPCVD工艺)、低压化学气相沉积(low pressure chemical vapor deposition,LPCVD)工艺(简称为LPCVD工艺)、电子束蒸发(electronic beam evaporation,EBE)工艺(简称为EBE工艺)和溅射沉积工艺中的任意一项。Among them, the deposition process can include atomic layer deposition (ALD) process (ALD process for short), plasma enhanced atomic layer deposition (PEALD) process (PEALD process for short), plasma enhanced Chemical vapor deposition (plasma enhanced chemical vapor deposition, PECVD) process (referred to as PECVD process), inductively coupled plasma chemical vapor deposition (ICPCVD) process (referred to as ICPCVD process), low pressure chemical vapor deposition (referred to as ICPCVD process) Any one of the low pressure chemical vapor deposition (LPCVD) process (referred to as LPCVD process), the electron beam evaporation (electronic beam evaporation, EBE) process (referred to as EBE process) and the sputtering deposition process.
进一步地,形成掺杂层之后,本申请提供的制备方法还可以包括:在外延层的表面形成介质层。对介质层进行光刻和刻蚀,形成第二凹槽。在第二凹槽内部形成第二电极层。Further, after forming the doping layer, the preparation method provided by this application may further include: forming a dielectric layer on the surface of the epitaxial layer. Photolithography and etching are performed on the dielectric layer to form a second groove. A second electrode layer is formed inside the second groove.
在一种可能的实现方式中,掺杂层、外延层和第一电极层均不同。也就是说,掺杂层与外延层之间存在明确的界限。掺杂层与第一电极层之间也存在明确的界限。In a possible implementation, the doping layer, the epitaxial layer and the first electrode layer are all different. That is, there is a clear boundary between doped layers and epitaxial layers. There is also a clear demarcation between the doped layer and the first electrode layer.
在另一种可能的实现方式中,掺杂层的材料可以为硅、氧化硅、氮化硅和氮氧化硅中的任意一种或多种。掺杂层的状态可以为单晶状态、多晶状态或非晶状态。掺杂层的厚度可以为1nm~50nm。通过掺杂层可以实现第一电极层与外延层的欧姆接触。当然,掺杂层的材料还可以为其他材料,掺杂层的厚度还可以为其他厚度范围,本申请不做限定。In another possible implementation, the material of the doping layer may be any one or more of silicon, silicon oxide, silicon nitride, and silicon oxynitride. The state of the doped layer may be a single crystal state, a polycrystalline state or an amorphous state. The thickness of the doped layer may be 1 nm to 50 nm. Ohmic contact between the first electrode layer and the epitaxial layer can be achieved through the doping layer. Of course, the material of the doped layer can also be other materials, and the thickness of the doped layer can also be in other thickness ranges, which is not limited in this application.
在一示例中,掺杂层从硅的峰值浓度降到硅浓度为10%的厚度小于20nm。其中,硅的峰值浓度可以为80%、70%、60%等。可以理解的,硅的浓度为峰值浓度的情况下,掺杂层可以对应一个厚度。硅的浓度为10%的情况下,掺杂层可以对应另一个厚度。两个厚度之间的厚度差可以小于20nm,能够减小第一电极层与外延层之间欧姆接触的接触电阻率。当然,两个厚度之间的厚度差会随着硅的浓度而改变,本申请对掺杂层从硅的峰值浓度降到硅浓度为10%的厚度不做限定。In one example, the doped layer is less than 20 nm thick from a peak concentration of silicon down to a silicon concentration of 10%. Among them, the peak concentration of silicon can be 80%, 70%, 60%, etc. It can be understood that when the concentration of silicon is the peak concentration, the doped layer can correspond to a thickness. In the case of a silicon concentration of 10%, the doped layer can correspond to another thickness. The thickness difference between the two thicknesses may be less than 20 nm, which can reduce the contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer. Of course, the thickness difference between the two thicknesses will change with the concentration of silicon. This application does not limit the thickness of the doped layer from the peak concentration of silicon to a silicon concentration of 10%.
在另一示例中,掺杂层从硅的第一浓度降到硅浓度为10%的厚度小于20nm。其中,第一浓度可以大于或等于60%。例如,第一浓度可以为70%或60%等。可以理解的,在硅的第一浓度的情况下,掺杂层可以对应一个厚度。在硅浓度为10%的情况下,掺杂层可以对应另一个厚度。两个厚度之间的厚度差可以小于20nm,能够减小第一电极层与外延层之间欧姆接触的接触电阻率。当然,两个厚度之间的厚度差会随着硅的浓度而改变,本申请对掺杂层从硅的第一浓度降到硅的第二浓度的厚度不做限定。In another example, the doped layer is less than 20 nm thick from a first concentration of silicon down to a silicon concentration of 10%. Wherein, the first concentration may be greater than or equal to 60%. For example, the first concentration may be 70% or 60%, etc. It can be understood that in the case of the first concentration of silicon, the doped layer may correspond to a thickness. In the case of a silicon concentration of 10%, the doped layer can correspond to another thickness. The thickness difference between the two thicknesses may be less than 20 nm, which can reduce the contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer. Of course, the thickness difference between the two thicknesses will change with the concentration of silicon. This application does not limit the thickness of the doped layer from the first concentration of silicon to the second concentration of silicon.
第三方面,本申请提供了一种半导体器件的制备方法,可以用于制备上述第一方面及其可能的实现方式提供的半导体器件。制备方法可以包括对介质层进行光刻,形成掩膜层。根据掩膜层形成掺杂层。在掺杂层的表面形成第一电极层,按照预设退火温度对第一电极层进行退火。其中,预设退火温度可以为400℃~800℃。In a third aspect, the present application provides a method for manufacturing a semiconductor device, which can be used to prepare the semiconductor device provided by the first aspect and its possible implementations. The preparation method may include photolithography of the dielectric layer to form a mask layer. The doped layer is formed according to the mask layer. A first electrode layer is formed on the surface of the doped layer, and the first electrode layer is annealed according to a preset annealing temperature. Among them, the preset annealing temperature can be 400°C to 800°C.
本申请提供的制备方法过程简洁,制备的半导体器件中第一电极层与外延层的欧姆接触的接触电阻率大幅度减小,接触电阻率可达到0.5Ω·mm,提高半导体器件的工作效率的同时,能够降低半导体器件的制备成本。The preparation method provided by this application has a simple process. The contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer in the prepared semiconductor device is greatly reduced, and the contact resistivity can reach 0.5Ω·mm, which improves the working efficiency of the semiconductor device. At the same time, the manufacturing cost of semiconductor devices can be reduced.
在一种可能的实现方式中,对介质层进行光刻,形成掩膜层,可以包括:在介质层表面涂光刻胶,并按照预设烘烤温度和预设烘烤时间对涂有光刻胶的介质层进行烘烤。按照预设曝光时间,对烘烤后的介质层进行曝光。采用显影液,并按照预设显影时间对曝光后的介质层进行显影,形成掩膜层。In one possible implementation, performing photolithography on the dielectric layer to form a mask layer may include: applying photoresist on the surface of the dielectric layer, and applying the photoresist on the surface of the dielectric layer according to the preset baking temperature and preset baking time. The medium layer is baked. Expose the baked dielectric layer according to the preset exposure time. Use a developing solution and develop the exposed dielectric layer according to the preset development time to form a mask layer.
其中,预设烘烤温度可以为90℃~120℃。预设烘烤时间可以为60s~120s,能够使液态的光刻胶在外延层表面固化。当然,预设烘烤温度还可以为其他温度范围,预设烘烤时间还可以为其他时间范围,本申请不做限定。Among them, the preset baking temperature can be 90°C to 120°C. The preset baking time can be 60s to 120s, which can solidify the liquid photoresist on the surface of the epitaxial layer. Of course, the preset baking temperature can also be in other temperature ranges, and the preset baking time can also be in other time ranges, which are not limited in this application.
可选地,预设曝光时间可以为100ms~1000ms,能够将掩模版上的图形转移转移到固化后的光刻胶上。当然,预设曝光时间还可以为其他时间范围,本申请不做限定。Optionally, the preset exposure time can be 100 ms to 1000 ms, which can transfer the pattern on the mask to the cured photoresist. Of course, the preset exposure time can also be in other time ranges, which is not limited in this application.
示例性的,显影液可以为四甲基氢氧化铵TMAH溶液。预设显影时间可以为30s~90s,可以将固化后的光刻胶上的图形转移至外延层上。当然,显影液还可以为其他溶液,预设显影时间还可以为其他时间范围,本申请不做限定。 For example, the developer may be a tetramethylammonium hydroxide TMAH solution. The preset development time can be 30s to 90s, and the pattern on the cured photoresist can be transferred to the epitaxial layer. Of course, the developer can also be other solutions, and the preset development time can also be other time ranges, which are not limited in this application.
在另一种可能的实现方式中,根据掩膜层形成掺杂层,可以包括:根据掩膜层对介质层进行刻蚀,形成第一凹槽。或者,根据掩膜层对介质层和部分外延层进行刻蚀,形成第一凹槽。也就是说,可以根据掩膜层只对介质层进行刻蚀,还可以根据掩膜层对介质层和部分外延层进行刻蚀,都可以形成第一凹槽。之后,可以采用沉积工艺在第一凹槽内部形成掺杂层。In another possible implementation, forming the doping layer according to the mask layer may include: etching the dielectric layer according to the mask layer to form a first groove. Alternatively, the dielectric layer and part of the epitaxial layer are etched according to the mask layer to form a first groove. That is to say, only the dielectric layer can be etched according to the mask layer, or the dielectric layer and part of the epitaxial layer can be etched according to the mask layer, and the first groove can be formed. Afterwards, a deposition process may be used to form a doped layer inside the first groove.
其中,沉积工艺可以包括ALD工艺、PEALD工艺、PECVD工艺、ICPCVD工艺、LPCVD工艺、EBE工艺和溅射沉积工艺中的任意一项。The deposition process may include any one of an ALD process, a PEALD process, a PECVD process, an ICPCVD process, a LPCVD process, an EBE process and a sputtering deposition process.
进一步地,在根据掩膜层形成掺杂层之前,本申请提供的制备方法还可以包括:按照预设处理时间,采用等离子体对外延层的表面进行处理。也就是说,在光刻外延层形成掩膜层之后,可以对外延层的表面进行处理,再形成掺杂层。能够增大外延层表面的粗糙度,进一步降低第一电极层与外延层的欧姆接触的接触电阻率。Further, before forming the doping layer according to the mask layer, the preparation method provided by this application may also include: using plasma to process the surface of the epitaxial layer according to a preset processing time. That is to say, after photolithography of the epitaxial layer to form the mask layer, the surface of the epitaxial layer can be processed and then a doped layer can be formed. The surface roughness of the epitaxial layer can be increased, and the contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer can be further reduced.
其中,预设处理时间可以为2min~60min。等离子体可以包括氢气H2、氮气N2、氨气NH3、氯气Cl2、氩气Ar和氧气O2中的任意一种或多种。Among them, the preset processing time can be 2min~60min. The plasma may include any one or more of hydrogen H 2 , nitrogen N 2 , ammonia NH 3 , chlorine Cl 2 , argon Ar and oxygen O 2 .
在按照预设退火温度对第一电极层进行退火之后,本申请提供的制备方法还可以包括:对介质层进行光刻和刻蚀,形成第二凹槽。在第二凹槽内部形成第二电极层。After annealing the first electrode layer according to the preset annealing temperature, the preparation method provided by this application may further include: performing photolithography and etching on the dielectric layer to form a second groove. A second electrode layer is formed inside the second groove.
在一种可能的实现方式中,掺杂层、外延层和第一电极层均不同。也就是说,掺杂层与外延层之间存在明确的界限。掺杂层与第一电极层之间也存在明确的界限。In a possible implementation, the doping layer, the epitaxial layer and the first electrode layer are all different. That is, there is a clear boundary between doped layers and epitaxial layers. There is also a clear demarcation between the doped layer and the first electrode layer.
在另一种可能的实现方式中,掺杂层的材料可以为硅、氧化硅、氮化硅和氮氧化硅中的任意一种或多种。掺杂层的状态可以为单晶状态、多晶状态或非晶状态。掺杂层的厚度可以为1nm~50nm。通过掺杂层可以实现第一电极层与外延层的欧姆接触。当然,掺杂层的材料还可以为其他材料,掺杂层的厚度还可以为其他厚度范围,本申请不做限定。In another possible implementation, the material of the doping layer may be any one or more of silicon, silicon oxide, silicon nitride, and silicon oxynitride. The state of the doped layer may be a single crystal state, a polycrystalline state or an amorphous state. The thickness of the doped layer may be 1 nm to 50 nm. Ohmic contact between the first electrode layer and the epitaxial layer can be achieved through the doping layer. Of course, the material of the doped layer can also be other materials, and the thickness of the doped layer can also be in other thickness ranges, which is not limited in this application.
在一示例中,掺杂层从硅的峰值浓度降到硅浓度为10%的厚度小于20nm。其中,硅的峰值浓度可以为80%、70%、60%等。可以理解的,硅的浓度为峰值浓度的情况下,掺杂层可以对应一个厚度。硅的浓度为10%的情况下,掺杂层可以对应另一个厚度。两个厚度之间的厚度差可以小于20nm,能够减小第一电极层与外延层之间欧姆接触的接触电阻率。当然,两个厚度之间的厚度差会随着硅的浓度而改变,本申请对掺杂层从硅的峰值浓度降到硅浓度为10%的厚度不做限定。In one example, the doped layer is less than 20 nm thick from a peak concentration of silicon down to a silicon concentration of 10%. Among them, the peak concentration of silicon can be 80%, 70%, 60%, etc. It can be understood that when the concentration of silicon is the peak concentration, the doped layer can correspond to a thickness. In the case of a silicon concentration of 10%, the doped layer can correspond to another thickness. The thickness difference between the two thicknesses may be less than 20 nm, which can reduce the contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer. Of course, the thickness difference between the two thicknesses will change with the concentration of silicon. This application does not limit the thickness of the doped layer from the peak concentration of silicon to a silicon concentration of 10%.
在另一示例中,掺杂层从硅的第一浓度降到硅浓度为10%的厚度小于20nm。其中,第一浓度可以大于或等于60%。例如,第一浓度可以为70%或60%等。可以理解的,在硅的第一浓度的情况下,掺杂层可以对应一个厚度。在硅的第二浓度的情况下,掺杂层可以对应另一个厚度。两个厚度之间的厚度差可以小于20nm,能够减小第一电极层与外延层之间欧姆接触的接触电阻率。当然,两个厚度之间的厚度差会随着硅的浓度而改变,本申请对掺杂层从硅的第一浓度降到硅的第二浓度的厚度不做限定。In another example, the doped layer is less than 20 nm thick from a first concentration of silicon down to a silicon concentration of 10%. Wherein, the first concentration may be greater than or equal to 60%. For example, the first concentration may be 70% or 60%, etc. It can be understood that in the case of the first concentration of silicon, the doped layer may correspond to a thickness. In the case of a second concentration of silicon, the doped layer can correspond to another thickness. The thickness difference between the two thicknesses may be less than 20 nm, which can reduce the contact resistivity of the ohmic contact between the first electrode layer and the epitaxial layer. Of course, the thickness difference between the two thicknesses will change with the concentration of silicon. This application does not limit the thickness of the doped layer from the first concentration of silicon to the second concentration of silicon.
第四方面,本申请提供了一种电子芯片,可以包括无源器件和上述第一方面及其可能的实现方式提供的半导体器件。其中,无源器件可以与半导体器件电连接。In a fourth aspect, the present application provides an electronic chip, which may include passive devices and the semiconductor device provided by the above-mentioned first aspect and its possible implementations. Among them, the passive device can be electrically connected to the semiconductor device.
可选地,无源器件可以为电阻、电容等。当然,无源器件还可以为其他器件,本申请不做限定。Optionally, passive components may be resistors, capacitors, etc. Of course, the passive components can also be other components, which are not limited in this application.
第五方面,本申请提供了一种电子设备,可以包括电路板和上述第四方面及其可能的实现方式提供的电子芯片。其中,电子芯片可以设置在电路板上。In a fifth aspect, the present application provides an electronic device, which may include a circuit board and the electronic chip provided in the fourth aspect and possible implementations thereof. Among them, the electronic chip can be arranged on the circuit board.
应当理解的是,本申请的第二方面至第五方面与本申请的第一方面的技术方案一致,各方面及对应的可行实施方式所取得的有益效果相似,不再赘述。It should be understood that the second to fifth aspects of the present application are consistent with the technical solution of the first aspect of the present application, and the beneficial effects achieved by each aspect and corresponding feasible implementations are similar, and will not be described again.
附图说明Description of drawings
为了更清楚地说明本申请或现有技术中的技术方案,下面将对实施例或现有技术描述中所需要使用的附图进行简单介绍,显而易见地,下面描述中的附图是本申请的一些实施例,对于本领域普通技术人员来讲,在不付出创造性劳动性的前提下,还可以根据这些附图获得其他的附图。In order to more clearly illustrate the technical solutions in this application or the prior art, the following will briefly introduce the drawings that need to be used in the description of the embodiments or the prior art. Obviously, the drawings in the following description are of the present application. For some embodiments, for those of ordinary skill in the art, other drawings can be obtained based on these drawings without exerting creative efforts.
图1为本申请实施例中半导体器件1的一种示意性结构图;Figure 1 is a schematic structural diagram of a semiconductor device 1 in an embodiment of the present application;
图2为本申请实施例中凹槽A的一种示意性结构图;Figure 2 is a schematic structural diagram of groove A in the embodiment of the present application;
图3为本申请实施例中凹槽A的另一种示意性结构图;Figure 3 is another schematic structural diagram of groove A in the embodiment of the present application;
图4为本申请实施例中凹槽A的另一种示意性结构图;Figure 4 is another schematic structural diagram of groove A in the embodiment of the present application;
图5为本申请实施例中凹槽A的另一种示意性结构图;Figure 5 is another schematic structural diagram of groove A in the embodiment of the present application;
图6为本申请实施例中凹槽A的另一种示意性结构图; Figure 6 is another schematic structural diagram of groove A in the embodiment of the present application;
图7为本申请实施例中凹槽A的另一种示意性结构图;Figure 7 is another schematic structural diagram of groove A in the embodiment of the present application;
图8为本申请实施例中半导体器件1的另一种示意性结构图;Figure 8 is another schematic structural diagram of the semiconductor device 1 in the embodiment of the present application;
图9为本申请实施例中半导体器件1的制备方法的一种示意性流程图;Figure 9 is a schematic flow chart of a method for manufacturing the semiconductor device 1 in the embodiment of the present application;
图10为本申请实施例中对外延层20进行光刻形成掩膜层70的一种示意性结构图;Figure 10 is a schematic structural diagram of the mask layer 70 formed by photolithography on the epitaxial layer 20 in the embodiment of the present application;
图11为本申请实施例中对外延层20进行光刻形成掩膜层70的一种示意性流程图;Figure 11 is a schematic flow chart of photolithography of the epitaxial layer 20 to form the mask layer 70 in an embodiment of the present application;
图12为本申请实施例中根据掩膜层70形成掺杂层30的一种示意性流程图;Figure 12 is a schematic flow chart of forming the doping layer 30 according to the mask layer 70 in the embodiment of the present application;
图13为本申请实施例中对外延层20进行刻蚀形成凹槽A的一种示意性结构图;Figure 13 is a schematic structural diagram of etching the epitaxial layer 20 to form a groove A in an embodiment of the present application;
图14为本申请实施例中对凹槽A进行处理的一种示意性结构图;Figure 14 is a schematic structural diagram of processing groove A in the embodiment of the present application;
图15为本申请实施例中根据掩膜层70形成掺杂层30的一种示意性结构图;Figure 15 is a schematic structural diagram of forming the doping layer 30 according to the mask layer 70 in the embodiment of the present application;
图16为本申请实施例中根据掩膜层70形成掺杂层30的另一种示意性流程图;Figure 16 is another schematic flow chart of forming the doping layer 30 according to the mask layer 70 in the embodiment of the present application;
图17为本申请实施例中对外延层20表面进行处理的一种示意性结构图;Figure 17 is a schematic structural diagram of processing the surface of the epitaxial layer 20 in the embodiment of the present application;
图18为本申请实施例中在外延层20表面形成掺杂层30的一种示意性结构图;Figure 18 is a schematic structural diagram of forming the doping layer 30 on the surface of the epitaxial layer 20 in the embodiment of the present application;
图19为本申请实施例中在掺杂层30的表面形成电极层50的一种示意性结构图;Figure 19 is a schematic structural diagram of forming the electrode layer 50 on the surface of the doped layer 30 in the embodiment of the present application;
图20为本申请实施例中去除掩膜层70的一种示意性结构图;Figure 20 is a schematic structural diagram of removing the mask layer 70 in the embodiment of the present application;
图21为本申请实施例中去除掩膜层70的另一种示意性结构图;Figure 21 is another schematic structural diagram of removing the mask layer 70 in the embodiment of the present application;
图22为本申请实施例中形成栅极层60的一种示意性流程图;Figure 22 is a schematic flow chart for forming the gate layer 60 in an embodiment of the present application;
图23为本申请实施例中形成介质层40的一种示意性结构图;Figure 23 is a schematic structural diagram of forming the dielectric layer 40 in the embodiment of the present application;
图24为本申请实施例中形成凹槽B的一种示意性结构图;Figure 24 is a schematic structural diagram of forming groove B in the embodiment of the present application;
图25为本申请实施例中半导体器件1的制备方法的另一种示意性流程图;Figure 25 is another schematic flow chart of the method of manufacturing the semiconductor device 1 in the embodiment of the present application;
图26为本申请实施例中半导体器件1的制备方法的又一种示意性流程图;Figure 26 is another schematic flow chart of the preparation method of the semiconductor device 1 in the embodiment of the present application;
图27为本申请实施例中半导体器件1的制备方法的又一种示意性流程图;Figure 27 is another schematic flow chart of the preparation method of the semiconductor device 1 in the embodiment of the present application;
图28为本申请实施例中在外延层20的表面形成介质层40的一种示意性结构图;Figure 28 is a schematic structural diagram of forming the dielectric layer 40 on the surface of the epitaxial layer 20 in the embodiment of the present application;
图29为本申请实施例中对介质层40进行光刻形成掩膜层70的一种示意性流程图;Figure 29 is a schematic flow chart of photolithography of the dielectric layer 40 to form the mask layer 70 in an embodiment of the present application;
图30为本申请实施例中对介质层40进行光刻形成掩膜层70的一种示意性结构图;Figure 30 is a schematic structural diagram of the mask layer 70 formed by photolithography on the dielectric layer 40 in the embodiment of the present application;
图31为本申请实施例中对介质层40和部分外延层20进行刻蚀形成凹槽A的一种示意性结构图;Figure 31 is a schematic structural diagram of etching the dielectric layer 40 and part of the epitaxial layer 20 to form a groove A in an embodiment of the present application;
图32为本申请实施例中去除掩膜层70的又一种示意性结构图;Figure 32 is another schematic structural diagram of removing the mask layer 70 in the embodiment of the present application;
图33为本申请实施例中对凹槽A进行处理的另一种示意性结构图;Figure 33 is another schematic structural diagram of processing groove A in the embodiment of the present application;
图34为本申请实施例中在凹槽A内部形成掺杂层30的一种示意性结构图;Figure 34 is a schematic structural diagram of forming the doping layer 30 inside the groove A in the embodiment of the present application;
图35为本申请实施例中对介质层40进行刻蚀形成凹槽A一种示意性结构图;Figure 35 is a schematic structural diagram of etching the dielectric layer 40 to form a groove A in the embodiment of the present application;
图36为本申请实施例中在凹槽A内部形成掺杂层30的另一种示意性结构图;Figure 36 is another schematic structural diagram of forming the doping layer 30 inside the groove A in the embodiment of the present application;
图37为本申请实施例中半导体器件1的制备方法的又一种示意性流程图。FIG. 37 is another schematic flow chart of a method for manufacturing the semiconductor device 1 in the embodiment of the present application.
具体实施方式Detailed ways
下面将结合附图,对本申请中的技术方案进行描述。The technical solutions in this application will be described below with reference to the accompanying drawings.
本申请的说明书实施例和权利要求书及附图中的术语“第一”、“第二”等仅用于区分描述的目的,而不能理解为指示或暗示相对重要性,也不能理解为指示或暗示顺序。此外,术语“包括”和“具有”以及他们的任何变形,意图在于覆盖不排他的包含,例如,包含了一系列步骤或单元。方法、系统、产品或设备不必限于清楚地列出的那些步骤或单元,而是可包括没有清楚地列出的或对于这些过程、方法、产品或设备固有的其它步骤或单元。The terms "first", "second", etc. in the description, embodiments, claims and drawings of this application are only used for the purpose of distinguishing and describing, and cannot be understood as indicating or implying relative importance, nor can they be understood as indicating. Or suggestive order. Furthermore, the terms "including" and "having" and any variations thereof are intended to cover a non-exclusive inclusion, for example, the inclusion of a series of steps or units. Methods, systems, products or devices are not necessarily limited to those steps or elements expressly listed, but may include other steps or elements not expressly listed or inherent to such processes, methods, products or devices.
应当理解,在本申请中,“至少一个(项)”是指一个或者多个,“多个”是指两个或两个以上。“和/或”,用于描述关联对象的关联关系,表示可以存在三种关系,例如,“A和/或B”可以表示:只存在A,只存在B以及同时存在A和B三种情况,其中A,B可以是单数或者复数。字符“/”一般表示前后关联对象是一种“或”的关系。“以下至少一项(个)”或其类似表达,是指这些项中的任意组合,包括单项(个)或复数项(个)的任意组合。例如,a,b或c中的至少一项(个),可以表示:a,b,c,“a和b”,“a和c”,“b和c”,或“a和b和c”,其中a,b,c可以是单个,也可以是多个。It should be understood that in this application, "at least one (item)" refers to one or more, and "plurality" refers to two or more. "And/or" is used to describe the relationship between associated objects, indicating that there can be three relationships. For example, "A and/or B" can mean: only A exists, only B exists, and A and B exist simultaneously. , where A and B can be singular or plural. The character "/" generally indicates that the related objects are in an "or" relationship. “At least one of the following” or similar expressions thereof refers to any combination of these items, including any combination of a single item (items) or a plurality of items (items). For example, at least one of a, b or c can mean: a, b, c, "a and b", "a and c", "b and c", or "a and b and c" ”, where a, b, c can be single or multiple.
随着科技的飞速发展,半导体器件(如高电子迁移率晶体管等)在手机、平板电脑等电子设备中得到了广泛的应用。相关技术提供的半导体器件往往通过电极层(如源极层和漏极层)的金属种类与配比、外延层的厚度等形成电极层与外延层的欧姆接触。但是,欧姆接触的电阻率较高,通常会大于 1Ω·mm,不利于减小半导体器件的导通电阻。With the rapid development of science and technology, semiconductor devices (such as high electron mobility transistors, etc.) have been widely used in electronic devices such as mobile phones and tablet computers. Semiconductor devices provided by related technologies often form ohmic contact between the electrode layer and the epitaxial layer through the metal type and ratio of the electrode layer (such as the source layer and the drain layer), the thickness of the epitaxial layer, etc. However, the resistivity of ohmic contacts is higher, usually greater than 1Ω·mm, which is not conducive to reducing the on-resistance of semiconductor devices.
为了克服上述不足,本申请实施例提供了一种半导体器件,如图1所示。半导体器件1可以包括衬底10、外延层20、掺杂层30、介质层40和电极层(即第一电极层)50。其中,电极层50可以包括源极层51和漏极层52。In order to overcome the above shortcomings, embodiments of the present application provide a semiconductor device, as shown in Figure 1 . The semiconductor device 1 may include a substrate 10, an epitaxial layer 20, a doped layer 30, a dielectric layer 40 and an electrode layer (ie, a first electrode layer) 50. The electrode layer 50 may include a source layer 51 and a drain layer 52 .
可选地,衬底10、外延层20和介质层40可以层叠设置。由于外延层20可以包括层叠设置的沟道层21、势垒层22和盖帽层23,因此也可以认为,衬底10、沟道层21、势垒层22、盖帽层23和介质层40层叠设置。Alternatively, the substrate 10, the epitaxial layer 20 and the dielectric layer 40 may be stacked. Since the epitaxial layer 20 may include a stacked channel layer 21 , a barrier layer 22 and a cap layer 23 , it can also be considered that the substrate 10 , the channel layer 21 , the barrier layer 22 , the cap layer 23 and the dielectric layer 40 are stacked set up.
可选地,外延层20中还可设置其他层,和/或,衬底10、外延层20和介质层40两两之间还可设置其他层,本申请实施例对此不做限定。Optionally, other layers may be disposed in the epitaxial layer 20 , and/or other layers may be disposed between the substrate 10 , the epitaxial layer 20 and the dielectric layer 40 , which are not limited in the embodiments of the present application.
半导体器件1可以设置凹槽A(即第一凹槽,图1中未标出)。掺杂层30和电极层50的一部分可以层叠设置于凹槽A中。也就是说,电极层50的一部分和掺杂层30层叠设置于凹槽A中,电极层50的另一部分可以设置于凹槽A外部。于是,通过掺杂层30可以形成电极层50与外延层20的欧姆接触。需要解释的是,欧姆接触是指电极层50与外延层20相接触的情况下,在接触界面处形成非常小的接触势垒,或在接触界面处未形成接触势垒。也就是说,欧姆接触的接触电阻率较低。欧姆接触也可以叫作非整流接触。The semiconductor device 1 may be provided with a groove A (ie, a first groove, not marked in FIG. 1 ). The doped layer 30 and a part of the electrode layer 50 may be stacked and disposed in the groove A. That is to say, a part of the electrode layer 50 and the doping layer 30 are stacked and arranged in the groove A, and another part of the electrode layer 50 may be arranged outside the groove A. Therefore, the ohmic contact between the electrode layer 50 and the epitaxial layer 20 can be formed through the doped layer 30 . It should be explained that ohmic contact means that when the electrode layer 50 is in contact with the epitaxial layer 20, a very small contact barrier is formed at the contact interface, or no contact barrier is formed at the contact interface. That is, an ohmic contact has a lower contact resistivity. Ohmic contact can also be called non-rectifying contact.
需要说明的是,电极层50可以包括源极层51和漏极层52,因此,半导体器件1设置的凹槽A可以有2个,其中一个用于放置掺杂层30和源极层51,另一个用于放置掺杂层30和漏极层52。It should be noted that the electrode layer 50 may include a source layer 51 and a drain layer 52. Therefore, the semiconductor device 1 may have two grooves A, one of which is used to place the doping layer 30 and the source layer 51. The other is used to place doped layer 30 and drain layer 52.
从图1可以看出,源极层51的下部分可以和掺杂层30层叠设置于一个凹槽A中,源极层51的上部分可以设置于一个凹槽A外部。类似的,漏极层52的下部分可以和掺杂层30层叠设置于另一个凹槽A中,漏极层52的上部分可以设置于另一个凹槽A外部。As can be seen from FIG. 1 , the lower part of the source layer 51 can be stacked with the doping layer 30 and disposed in a groove A, and the upper part of the source layer 51 can be disposed outside the groove A. Similarly, the lower part of the drain layer 52 may be stacked with the doping layer 30 and disposed in another groove A, and the upper part of the drain layer 52 may be disposed outside the other groove A.
本申请实施例提供的半导体器件1通过掺杂层30形成电极层50与外延层20的欧姆接触,减小了欧姆接触的接触电阻率,有助于减小半导体器件的导通电阻,进而降低半导体器件的功率损耗。The semiconductor device 1 provided by the embodiment of the present application forms an ohmic contact between the electrode layer 50 and the epitaxial layer 20 through the doping layer 30, which reduces the contact resistivity of the ohmic contact, helps to reduce the on-resistance of the semiconductor device, and thereby reduces the Power losses in semiconductor devices.
在一种可能的实现方式中,介质层40可以设有凹槽B(即第二凹槽,图1中未标出)。凹槽B的底部可以位于盖帽层23的表面。其中,盖帽层23的表面可以用于指示盖帽层23背离势垒层22的表面,也就是图1中盖帽层23的上表面。In a possible implementation, the dielectric layer 40 may be provided with groove B (ie, the second groove, not marked in FIG. 1 ). The bottom of the groove B may be located on the surface of the capping layer 23 . The surface of the cap layer 23 may be used to indicate the surface of the cap layer 23 facing away from the barrier layer 22 , that is, the upper surface of the cap layer 23 in FIG. 1 .
进一步地,参考图1,半导体器件1还可以包括栅极层60(即第二电极层),栅极层60可以位于凹槽B内部。栅极层60与盖帽层23可以形成肖特基接触。需要解释的是,肖特基接触是指栅极层60和盖帽层23相接触的情况下,在接触界面处盖帽层23的能带弯曲,形成接触势垒(可以叫作肖特基势垒)。肖特基接触也可以叫作整流接触。Further, referring to FIG. 1 , the semiconductor device 1 may further include a gate layer 60 (ie, a second electrode layer), and the gate layer 60 may be located inside the groove B. The gate layer 60 and the cap layer 23 may form a Schottky contact. It should be explained that Schottky contact means that when the gate layer 60 and the cap layer 23 are in contact, the energy band of the cap layer 23 bends at the contact interface, forming a contact barrier (which can be called a Schottky barrier). ). Schottky contact can also be called rectifying contact.
在另一种可能的实现方式中,如图1所示,掺杂层30、外延层20和电极层50均不同。也就是说,掺杂层30与外延层20(可以为盖帽层23、势垒层22或沟道层21)之间存在明确的界限。掺杂层30与电极层50(即掺杂层30与源极层51,掺杂层30与漏极层52)之间也存在明确的界限。In another possible implementation, as shown in FIG. 1 , the doping layer 30 , the epitaxial layer 20 and the electrode layer 50 are all different. That is to say, there is a clear boundary between the doped layer 30 and the epitaxial layer 20 (which can be the cap layer 23, the barrier layer 22 or the channel layer 21). There are also clear boundaries between the doping layer 30 and the electrode layer 50 (ie, the doping layer 30 and the source layer 51, and the doping layer 30 and the drain layer 52).
在一示例中,衬底10的材料可以为硅Si(silicon)(可以是含掺杂的硅或者不含掺杂的硅)、碳化硅SiC(silicon carbide)、蓝宝石(sapphire)等各项材料中的任意一种或多种。当然,衬底1的材料还可以为其他材料,本申请实施例不做限定。In an example, the material of the substrate 10 may be silicon (silicon) (which may be doped silicon or non-doped silicon), silicon carbide (SiC), sapphire (sapphire), and other materials. any one or more of them. Of course, the material of the substrate 1 can also be other materials, which are not limited in the embodiments of this application.
在另一示例中,外延层20可以为半导体器件工艺中直接生长在衬底10上的部分。In another example, epitaxial layer 20 may be a portion grown directly on substrate 10 in a semiconductor device process.
其中,外延层20中的沟道层21的厚度可以为100nm~500nm,沟道层21的材料可以为氮化镓GaN(gallium nitride)。当然,沟道层21的厚度还可以为其他厚度范围,沟道层21的材料还可以为其他材料,本申请实施例不做限定。The thickness of the channel layer 21 in the epitaxial layer 20 may be 100 nm to 500 nm, and the material of the channel layer 21 may be gallium nitride (gallium nitride). Of course, the thickness of the channel layer 21 can also be in other thickness ranges, and the material of the channel layer 21 can also be other materials, which are not limited in the embodiments of this application.
本申请实施例中,沟道层21与外延层20中势垒层22直接可以产生二维电子气(two-dimensional electron gas,2DEG),如图1所示。需要说明的是,可以用量子限制等物理方法使电子群在一个方向上的运动被局限于一个很小的范围内,而在另外二个方向上可以自由运动的系统称为二维电子系统。于是,可以将二维电子系统中密度较低的电子称为二维电子气。沟道层21可以提高二维电子气的浓度,提高半导体器件1的电流密度,进而提高半导体器件1的输出电流。In the embodiment of the present application, the barrier layer 22 in the channel layer 21 and the epitaxial layer 20 can directly generate two-dimensional electron gas (2DEG), as shown in Figure 1 . It should be noted that physical methods such as quantum confinement can be used to limit the movement of the electron group in one direction to a small range, while a system that can move freely in the other two directions is called a two-dimensional electronic system. Therefore, the electrons with lower density in the two-dimensional electron system can be called two-dimensional electron gas. The channel layer 21 can increase the concentration of the two-dimensional electron gas, increase the current density of the semiconductor device 1 , and thereby increase the output current of the semiconductor device 1 .
在又一些实施例中,势垒层22的材料可以为铝镓氮AlGaN(aluminum gallium nitride),势垒层22的厚度可以为15nm~40nm。由于势垒层22与沟道层21各自的材料不同,因此两者可以形成异质结。例如,势垒层22的材料可以为铝镓氮AlGaN,沟道层21的材料可以为氮化镓GaN。于是,势垒层22和沟道层21之间可以形成异质结。在异质结的界面处可以获得二维电子气。 In some embodiments, the barrier layer 22 may be made of aluminum gallium nitride (AlGaN), and the barrier layer 22 may have a thickness of 15 nm to 40 nm. Since the materials of the barrier layer 22 and the channel layer 21 are different, they can form a heterojunction. For example, the barrier layer 22 may be made of aluminum gallium nitride AlGaN, and the channel layer 21 may be made of gallium nitride GaN. Thus, a heterojunction can be formed between the barrier layer 22 and the channel layer 21 . Two-dimensional electron gas can be obtained at the interface of the heterojunction.
需要说明的是,势垒层22的材料还可以为铟铝氮InAlN(indium aluminum nitride)、铟镓氮InGaN(indium gallium nitride)和铝铟铝氮AlInGaN(aluminum indium gallium nitride)中的任意一种,或前述材料(包括铝镓氮AlGaN)的任意组合。于是,势垒层22的厚度可以为5nm~20nm。同样,势垒层22与沟道层21可以形成异质结。It should be noted that the material of the barrier layer 22 can also be any one of InAlN (indium aluminum nitride), InGaN (indium gallium nitride), and AlInGaN (aluminum indium gallium nitride). , or any combination of the aforementioned materials (including aluminum gallium nitride AlGaN). Therefore, the thickness of the barrier layer 22 may be 5 nm to 20 nm. Similarly, the barrier layer 22 and the channel layer 21 may form a heterojunction.
还需要说明的是,势垒层22的材料可以为其他材料,势垒层22的厚度还可以为其他厚度范围,本申请实施例不做限定。It should also be noted that the material of the barrier layer 22 can be other materials, and the thickness of the barrier layer 22 can also be in other thickness ranges, which are not limited in the embodiments of this application.
在又一些实施例中,外延层20中盖帽层23的材料可以为GaN,盖帽层23的厚度可以为1nm~5nm。盖帽层23可以用于防止势垒层22氧化,进而保护势垒层22的界面。当然,盖帽层23的材料还可以为其他材料,盖帽层23的厚度还可以为其他厚度范围,本申请实施例不做限定。In some embodiments, the material of the cap layer 23 in the epitaxial layer 20 may be GaN, and the thickness of the cap layer 23 may be 1 nm to 5 nm. The cap layer 23 can be used to prevent the barrier layer 22 from being oxidized, thereby protecting the interface of the barrier layer 22 . Of course, the material of the capping layer 23 can also be other materials, and the thickness of the capping layer 23 can also be in other thickness ranges, which are not limited in the embodiments of this application.
在又一些实施例中,源极层51的材料可以采用钛Ti(titanium)、金Au(aurum)和铝Al(Aluminium)等各项材料中的任意一种或多种。也就是说,源极层51可以采用Ti、Au或Al,还可以采用Ti、Au和Al中至少两种金属的合金。In some embodiments, the source layer 51 may be made of any one or more of various materials such as titanium (titanium), gold (aurum), and aluminum (Al). That is to say, the source layer 51 may be made of Ti, Au or Al, or may be made of an alloy of at least two metals among Ti, Au and Al.
类似的,漏极层52的材料也可以采用钛Ti(titanium)、金Au(aurum)和铝Al(Aluminium)等各项材料中的任意一种或多种。Similarly, the material of the drain layer 52 may also be any one or more of various materials such as titanium (Titanium), gold (Au) (aurum), and aluminum (Al).
栅极层60可以采用Ti、Au和镍Ni(nickel)等各项材料中的任意一种或多种。也就是说,栅极层60可以采用Ti、Au或Ni,还可以采用Ti、Au和Ni中至少两种金属的合金。The gate layer 60 may be made of any one or more of various materials such as Ti, Au, and nickel (nickel). That is to say, the gate layer 60 may be made of Ti, Au or Ni, or may be made of an alloy of at least two metals among Ti, Au and Ni.
当然,源极层51、漏极层52和栅极层60的材料还可以分别其他材料,本申请实施例不做限定。Of course, the source layer 51 , the drain layer 52 and the gate layer 60 can also be made of other materials, which are not limited in the embodiments of this application.
本申请实施例中,源极层51和漏极层52的材料相同,两者分别采用Ti、Al和Au的合金。而且,可以以Ti、Al、Ti、Au的顺序层叠设置,对应的厚度分别为20nm、150nm、30nm、50nm。In the embodiment of the present application, the source layer 51 and the drain layer 52 are made of the same material, and they are alloys of Ti, Al and Au respectively. Moreover, Ti, Al, Ti, and Au can be stacked in the order, and the corresponding thicknesses are 20nm, 150nm, 30nm, and 50nm respectively.
在又一些实施例中,掺杂层30的材料可以为Si、氧化硅SiO2(silicon dioxide)、氮化硅SiN(silicon nitride)和氮氧化硅SiON(silicon oxynitride)中的任意一种或多种。掺杂层30的厚度可以为1nm~50nm。另外,掺杂层30的状态可以为单晶状态、多晶状态或非晶状态。通过掺杂层30可以实现源极层51与外延层20的欧姆接触以及漏极层52与外延层20的欧姆接触。当然,掺杂层30的材料还可以为其他材料,掺杂层30的厚度还可以为其他厚度范围,本申请实施例不做限定。In some embodiments, the material of the doping layer 30 may be any one or more of Si, silicon oxide SiO 2 (silicon dioxide), silicon nitride SiN (silicon nitride), and silicon oxynitride SiON (silicon oxynitride). kind. The thickness of the doped layer 30 may be 1 nm to 50 nm. In addition, the state of the doped layer 30 may be a single crystal state, a polycrystalline state, or an amorphous state. The doped layer 30 can realize the ohmic contact between the source layer 51 and the epitaxial layer 20 and the ohmic contact between the drain layer 52 and the epitaxial layer 20 . Of course, the material of the doped layer 30 can also be other materials, and the thickness of the doped layer 30 can also be in other thickness ranges, which are not limited in the embodiments of this application.
在一个实施例中,掺杂层30的厚度可以为5nm。掺杂层30的材料可以为Si,状态为多晶状态,也就是说,掺杂层30为多晶硅。In one embodiment, the thickness of doped layer 30 may be 5 nm. The material of the doped layer 30 may be Si, and the state may be a polycrystalline state. That is to say, the doped layer 30 may be polycrystalline silicon.
进一步地,掺杂层30从硅的峰值浓度(可以为80%、70%、60%等)降到硅浓度为10%的厚度小于20nm。可以理解的,硅的浓度为峰值浓度的情况下,掺杂层30可以对应一个厚度。硅的浓度为10%的情况下,掺杂层30可以对应另一个厚度。两个厚度之间的厚度差可以为20nm。当然,两个厚度之间的厚度差会随着硅的浓度而改变,本申请实施例对掺杂层30从硅的峰值浓度降到硅浓度为10%的厚度不做限定。Further, the thickness of the doped layer 30 decreases from the peak concentration of silicon (which can be 80%, 70%, 60%, etc.) to the silicon concentration of 10%, which is less than 20 nm. It can be understood that when the concentration of silicon is the peak concentration, the doped layer 30 can correspond to a thickness. In the case where the silicon concentration is 10%, the doped layer 30 may correspond to another thickness. The thickness difference between the two thicknesses can be 20nm. Of course, the thickness difference between the two thicknesses will change with the concentration of silicon. The embodiment of the present application does not limit the thickness of the doped layer 30 from the peak concentration of silicon to a silicon concentration of 10%.
当然,还可以设定掺杂层30中硅的第一浓度为60%,硅的第二浓度为10%。那么,掺杂层30从硅的第一浓度降到硅的第二浓度的厚度可以小于20nm。当然,硅的第一浓度和第二浓度还可以分别为其他浓度,掺杂层30从硅的第一浓度降到硅的第二浓度的厚度也可以为其他厚度范围,本申请实施例不做限定。Of course, the first concentration of silicon in the doped layer 30 can also be set to 60%, and the second concentration of silicon is 10%. Then, the thickness of the doped layer 30 from the first concentration of silicon to the second concentration of silicon may be less than 20 nm. Of course, the first concentration and the second concentration of silicon can also be other concentrations respectively, and the thickness of the doping layer 30 from the first concentration of silicon to the second concentration of silicon can also be in other thickness ranges, which are not covered in the embodiments of this application. limited.
在又一些实施例中,介质层40可以包括一层介质层。那么,介质层40的材料可以为SiO2或SiN等,厚度可以为10nm~500nm。In still other embodiments, dielectric layer 40 may include a dielectric layer. Then, the material of the dielectric layer 40 may be SiO 2 or SiN, etc., and the thickness may be 10 nm to 500 nm.
介质层40也可以包括两层层叠设置的介质层。那么,其中一层介质层的材料可以为SiO2,另一层介质层的材料可以为SiN。或者,其中一层介质层的材料可以为Al2O3,另一层介质层的材料可以为SiN。当然,两层介质层的材料可以相同,可以都为SiO2或者SiN。两层介质层的厚度可以分别为5nm~500nm。能够增大介质层40的相对介电常数,进而提高了介质层40的绝缘性,减小了半导体器件1的静态电流,降低半导体器件1的静态功耗。当然,介质层40的材料还可以为其他材料,厚度也可以为其他厚度范围,本申请实施例不做限定。The dielectric layer 40 may also include two stacked dielectric layers. Then, one of the dielectric layers may be made of SiO 2 , and the other dielectric layer may be made of SiN. Alternatively, one of the dielectric layers may be made of Al 2 O 3 , and the other dielectric layer may be made of SiN. Of course, the material of the two dielectric layers can be the same, and both can be SiO 2 or SiN. The thickness of the two dielectric layers can be 5 nm to 500 nm respectively. The relative dielectric constant of the dielectric layer 40 can be increased, thereby improving the insulation of the dielectric layer 40 , reducing the quiescent current of the semiconductor device 1 , and reducing the quiescent power consumption of the semiconductor device 1 . Of course, the material of the dielectric layer 40 can also be other materials, and the thickness can also be in other thickness ranges, which are not limited in the embodiments of this application.
在本申请的一些实施例中,上述凹槽A的底部可以位于盖帽层23、势垒层22或沟道层21。可以参考以下图2至图7介绍凹槽A的位置。需要说明的是,为了清楚的描述凹槽A底部的位置,上述图2至图7中未示出电极层50。In some embodiments of the present application, the bottom of the above-mentioned groove A may be located at the cap layer 23 , the barrier layer 22 or the channel layer 21 . The location of groove A can be introduced with reference to Figures 2 to 7 below. It should be noted that, in order to clearly describe the position of the bottom of the groove A, the electrode layer 50 is not shown in the above-mentioned FIGS. 2 to 7 .
凹槽A底部的位置可以分以下几种情况:The position of the bottom of groove A can be divided into the following situations:
情况一:凹槽A的底部可以位于盖帽层23内部,如图2所示。或者,凹槽A的底部位于盖帽层 23的靠近介质层40的表面,如图3所示。也就是说,凹槽A的底部可以位于盖帽层23的内部或上表面。Case 1: The bottom of the groove A may be located inside the capping layer 23, as shown in Figure 2. Alternatively, the bottom of groove A is located on the capping layer 23 close to the surface of the dielectric layer 40, as shown in FIG. 3 . That is, the bottom of the groove A may be located inside or on the upper surface of the capping layer 23 .
于是,掺杂层30与盖帽层23可以发生化学反应,形成N型掺杂(如硅掺杂)区域。电极层50与N型掺杂区域发生化学反应,可形成低电阻率的欧姆接触。也就是说,实现了电极层50与盖帽层23的欧姆接触,且通过掺杂层30减小了欧姆接触的接触电阻率。Therefore, the doped layer 30 and the capping layer 23 can react chemically to form an N-type doped (such as silicon doped) region. The electrode layer 50 reacts chemically with the N-type doped region to form an ohmic contact with low resistivity. That is to say, ohmic contact between the electrode layer 50 and the cap layer 23 is achieved, and the contact resistivity of the ohmic contact is reduced through the doping layer 30 .
情况二:凹槽A的底部可以位于势垒层22的内部,如图4所示。或者,凹槽A的底部可以位于势垒层22的靠近盖帽层21的表面,如图5所示。也就是说,凹槽A的底部可以位于势垒层22的内部或上表面。Case 2: The bottom of the groove A may be located inside the barrier layer 22 , as shown in FIG. 4 . Alternatively, the bottom of the groove A may be located on the surface of the barrier layer 22 close to the capping layer 21, as shown in FIG. 5 . That is, the bottom of the groove A may be located inside or on the upper surface of the barrier layer 22 .
于是,掺杂层30与势垒层22可以发生化学反应,形成N型掺杂(如硅掺杂)区域。电极层50与N型掺杂区域发生化学反应,可形成低电阻率的欧姆接触。也就是说,实现了电极层50与势垒层22的欧姆接触,且通过掺杂层30减小了欧姆接触的接触电阻率。Therefore, the doping layer 30 and the barrier layer 22 can react chemically to form an N-type doped (eg silicon doped) region. The electrode layer 50 reacts chemically with the N-type doped region to form an ohmic contact with low resistivity. That is to say, ohmic contact between the electrode layer 50 and the barrier layer 22 is achieved, and the contact resistivity of the ohmic contact is reduced through the doping layer 30 .
情况三:凹槽A的底部可以位于沟道层21的内部,如图6所示。或者,凹槽A的底部可以位于沟道层21的靠近势垒层22的表面,如图7所示。也就是说,凹槽A的底部可以位于沟道层21的内部或上表面。Case 3: The bottom of the groove A may be located inside the channel layer 21, as shown in FIG. 6 . Alternatively, the bottom of the groove A may be located on a surface of the channel layer 21 close to the barrier layer 22, as shown in FIG. 7 . That is, the bottom of the groove A may be located inside or on the upper surface of the channel layer 21 .
于是,掺杂层30与沟道层21可以发生化学反应,形成N型掺杂(如硅掺杂)区域。电极层50与N型掺杂区域发生化学反应,可形成低电阻率的欧姆接触。也就是说,实现了电极层50与沟道层21的欧姆接触,且通过掺杂层30减小了欧姆接触的接触电阻率。Therefore, a chemical reaction can occur between the doped layer 30 and the channel layer 21 to form an N-type doped (such as silicon doped) region. The electrode layer 50 reacts chemically with the N-type doped region to form an ohmic contact with low resistivity. That is to say, ohmic contact between the electrode layer 50 and the channel layer 21 is achieved, and the contact resistivity of the ohmic contact is reduced through the doping layer 30 .
进一步地,凹槽A的底部与沟道层21的上表面距离10nm以内。那么,可以具有以下两种结构:Furthermore, the distance between the bottom of the groove A and the upper surface of the channel layer 21 is within 10 nm. Then, you can have the following two structures:
结构一:凹槽A的底部可以位于势垒层22内部且与沟道层21的上表面距离10nm以内,如图1所示。Structure 1: The bottom of the groove A can be located inside the barrier layer 22 and within a distance of 10 nm from the upper surface of the channel layer 21 , as shown in FIG. 1 .
结构二:凹槽A的底部可以位于沟道层21内部且与沟道层21的上表面距离10nm以内,如图8所示。Structure 2: The bottom of the groove A can be located inside the channel layer 21 and within a distance of 10 nm from the upper surface of the channel layer 21, as shown in Figure 8.
需要说明的是,上述两种结构同样可以实现电极层50与势垒层22的欧姆接触,或者实现电极层50与沟道层21的欧姆接触,且可以最大程度的降低欧姆接触的接触电阻率,可以将接触电阻率降低到0.5Ω·mm,提高半导体器件1的工作效率的同时,能够降低半导体器件1的制备成本。It should be noted that the above two structures can also realize ohmic contact between the electrode layer 50 and the barrier layer 22 , or realize ohmic contact between the electrode layer 50 and the channel layer 21 , and can minimize the contact resistivity of the ohmic contact. , the contact resistivity can be reduced to 0.5Ω·mm, which not only improves the working efficiency of the semiconductor device 1, but also reduces the preparation cost of the semiconductor device 1.
示例性的,本申请实施例提供的半导体器件1可以为场效应晶体管,进一步可以为高电子迁移率晶体管(high electron mobility transistor,HEMT)、异质结场效应晶体管(heterojunction field effect transistor,HFET)或者调制掺杂场效应管(modulation-doped FET,MODFET)。当然,半导体器件1还可以为其他类型的晶体管,本申请实施例不做限定。Illustratively, the semiconductor device 1 provided in the embodiment of the present application can be a field effect transistor, and further can be a high electron mobility transistor (HEMT) or a heterojunction field effect transistor (HFET). Or modulation-doped FET (MODFET). Of course, the semiconductor device 1 can also be other types of transistors, which are not limited in the embodiments of this application.
本申请实施例提供了一种半导体器件1的制备方法,如图9所示,制备过程100可以按照如下步骤实现:The embodiment of the present application provides a method for preparing a semiconductor device 1. As shown in Figure 9, the preparation process 100 can be implemented according to the following steps:
步骤S101:对外延层20进行光刻,形成掩膜层70,如图10所示。Step S101: Perform photolithography on the epitaxial layer 20 to form a mask layer 70, as shown in FIG. 10 .
进一步地,参考图11,步骤S101中对外延层20进行光刻形成掩膜层70可以进一步按照如下步骤实现:Further, referring to FIG. 11 , in step S101 , photolithography is performed on the epitaxial layer 20 to form the mask layer 70 , which can be further implemented as follows:
步骤S101a1:在外延层20(可以是外延层20的盖帽层23)表面涂光刻胶,并按照预设烘烤温度和预设烘烤时间对涂有光刻胶的外延层20进行烘烤。Step S101a1: Coat photoresist on the surface of the epitaxial layer 20 (which may be the capping layer 23 of the epitaxial layer 20), and bake the epitaxial layer 20 coated with photoresist according to the preset baking temperature and preset baking time.
可选地,预设烘烤温度可以为90℃~120℃。预设烘烤时间可以为60s~120s,使液态的光刻胶在外延层20表面固化。当然,预设烘烤温度还可以为其他温度范围,预设烘烤时间还可以为其他时间范围,本申请实施例不做限定。Optionally, the preset baking temperature may be 90°C to 120°C. The preset baking time can be 60 to 120 seconds to solidify the liquid photoresist on the surface of the epitaxial layer 20 . Of course, the preset baking temperature can also be in other temperature ranges, and the preset baking time can also be in other time ranges, which are not limited in the embodiments of this application.
本申请实施例中,在外延层20的表面涂光刻胶,在90℃的烘烤温度下对涂有光刻胶的外延层20烘烤90s。In the embodiment of the present application, photoresist is coated on the surface of the epitaxial layer 20, and the epitaxial layer 20 coated with the photoresist is baked for 90 seconds at a baking temperature of 90°C.
在一示例中,光刻胶可以是Az5214型光刻胶。当然,光刻胶还可以为其他类型,本申请实施例不做限定。In one example, the photoresist may be Az5214 type photoresist. Of course, the photoresist can also be of other types, which is not limited in the embodiments of this application.
步骤S101a2:按照预设曝光时间,对烘烤后的外延层20进行曝光。Step S101a2: Expose the baked epitaxial layer 20 according to the preset exposure time.
可选地,预设曝光时间可以为100ms~1000ms,能够将掩模版上的图形转移到固化后的光刻胶上。当然,预设曝光时间还可以为其他时间范围,本申请实施例不做限定。Optionally, the preset exposure time can be 100ms to 1000ms, which can transfer the pattern on the mask to the cured photoresist. Of course, the preset exposure time can also be in other time ranges, which is not limited in the embodiments of this application.
本申请实施例中,对烘烤后的外延层20曝光200ms。In the embodiment of the present application, the baked epitaxial layer 20 is exposed for 200 ms.
步骤S101a3:采用显影液,并按照预设显影时间对曝光后的外延层20进行显影,形成掩膜层70。 Step S101a3: Use a developer to develop the exposed epitaxial layer 20 according to a preset development time to form a mask layer 70.
在一示例中,显影液可以为四甲基氢氧化铵(tetramethylammonium hydroxide,TMAH)溶液(可以简称为TMAH溶液)。当然,显影液还可以为其他溶液,本申请实施例不做限定。In one example, the developer may be a tetramethylammonium hydroxide (TMAH) solution (which may be referred to as a TMAH solution). Of course, the developer can also be other solutions, which are not limited in the embodiments of this application.
在另一示例中,预设显影时间可以为30s~90s,可以将固化后的光刻胶上的图形转移至外延层20上。In another example, the preset development time may be 30 to 90 s, and the pattern on the cured photoresist may be transferred to the epitaxial layer 20 .
在本申请实施例中,可以采用TMAH溶液对曝光后的外延层20显影50s,形成厚度为1um的掩膜层70。In the embodiment of the present application, a TMAH solution can be used to develop the exposed epitaxial layer 20 for 50 seconds to form a mask layer 70 with a thickness of 1 μm.
再次参考图9,制备过程100还可以包括:Referring again to Figure 9, the preparation process 100 may also include:
步骤S102:根据掩膜层70形成掺杂层30,可以分为以下几种实施例进行介绍:Step S102: Forming the doping layer 30 according to the mask layer 70, which can be divided into the following embodiments for introduction:
在本申请的一些实施例中,如图12所示,按照以下步骤形成掺杂层30:In some embodiments of the present application, as shown in Figure 12, the doped layer 30 is formed according to the following steps:
步骤S102a1:根据图10的掩膜层70对部分外延层20进行刻蚀,形成凹槽A,如图13所示。Step S102a1: Etch part of the epitaxial layer 20 according to the mask layer 70 of FIG. 10 to form a groove A, as shown in FIG. 13.
可选地,可以采用干法刻蚀工艺或者湿法刻蚀工艺对部分外延层20刻蚀5min~100min。其中,干法刻蚀工艺可以包括反应离子刻蚀(reaction ion etch,RIE)工艺(简称RIE工艺)、电感耦合等离子体刻蚀(inductively coupling plasma etch,ICP)工艺(简称为ICP工艺)、离子束刻蚀(ion beam etching,IBE)工艺(简称为IBE工艺)、先进氧化物刻蚀(advanced oxide etch,AOE)工艺(简称为AOE工艺)中的任意一项。Alternatively, a dry etching process or a wet etching process may be used to etch part of the epitaxial layer 20 for 5 to 100 minutes. Among them, the dry etching process can include reactive ion etching (RIE) process (RIE process for short), inductively coupled plasma etching (ICP process for short), ion etching (ICP process for short), Any one of the ion beam etching (IBE) process (referred to as the IBE process) and the advanced oxide etch (AOE) process (referred to as the AOE process).
本申请实施例中,可以采用ICP工艺对部分外延层20刻蚀10min,通过电感耦合等离子体对部分外延层20的物理轰击,同时电感耦合等离子体与外延层20发生化学反应,实现双重作用的刻蚀,刻蚀速率快。In the embodiment of the present application, the ICP process can be used to etch part of the epitaxial layer 20 for 10 minutes, and the part of the epitaxial layer 20 is physically bombarded by the inductively coupled plasma. At the same time, a chemical reaction occurs between the inductively coupled plasma and the epitaxial layer 20 to achieve dual effects. Etching, the etching rate is fast.
步骤S102a2:可以按照预设处理时间,采用等离子体对凹槽A进行处理。Step S102a2: Plasma can be used to process the groove A according to the preset processing time.
本申请实施例中,可以采用Ar对凹槽A处理10min,不仅能够增大凹槽A的表面粗糙度,还可以增加凹槽A表面的N空位,进一步降低电极层50与外延层20的欧姆接触的接触电阻率。In the embodiment of the present application, Ar can be used to treat groove A for 10 minutes, which can not only increase the surface roughness of groove A, but also increase the N vacancies on the surface of groove A, further reducing the ohmic resistance of the electrode layer 50 and the epitaxial layer 20 Contact resistivity of the contact.
步骤S102a3:采用沉积工艺在凹槽A内部形成掺杂层30,如图14和图15所示。Step S102a3: Use a deposition process to form the doping layer 30 inside the groove A, as shown in Figures 14 and 15.
需要说明的是,掺杂层30的材料、状态和厚度等可以参考上文介绍,本申请实施例不再赘述。It should be noted that the material, state and thickness of the doping layer 30 can be referred to the above introduction, and will not be described again in the embodiment of the present application.
可选地,沉积工艺可以包括原子层沉积(atomic layer deposition,ALD)工艺(简称为ALD工艺)、等离子体增强原子层沉积(plasma enhanced atomic layer deposition,PEALD)工艺(简称为PEALD工艺)、等离子体增强化学气相沉积(plasma enhanced chemical vapor deposition,PECVD)工艺(简称为PECVD工艺)、电感耦合等离子体化学气相沉积(inductively coupled plasma chemical vapor deposition,ICPCVD)工艺(简称为ICPCVD工艺)、低压化学气相沉积(low pressure chemical vapor deposition,LPCVD)工艺(简称为LPCVD工艺)、电子束蒸发(electronic beam evaporation,EBE)工艺(简称为EBE工艺)和溅射沉积工艺中的任意一项。Optionally, the deposition process may include an atomic layer deposition (ALD) process (ALD process for short), plasma enhanced atomic layer deposition (PEALD) process (PEALD process for short), plasma Volume enhanced chemical vapor deposition (plasma enhanced chemical vapor deposition, PECVD) process (referred to as PECVD process), inductively coupled plasma chemical vapor deposition (inductively coupled plasma chemical vapor deposition, ICPCVD) process (referred to as ICPCVD process), low pressure chemical vapor deposition Any one of the deposition (low pressure chemical vapor deposition, LPCVD) process (referred to as the LPCVD process), the electron beam evaporation (electronic beam evaporation, EBE) process (referred to as the EBE process) and the sputter deposition process.
本申请实施例中,采用PECVD工艺在凹槽A内部沉积多晶硅,形成厚度为5nm的掺杂层30。In the embodiment of the present application, a PECVD process is used to deposit polysilicon inside the groove A to form a doped layer 30 with a thickness of 5 nm.
在本申请的另一些实施例中,如图16所示,按照以下步骤形成掺杂层30:In other embodiments of the present application, as shown in Figure 16, the doped layer 30 is formed according to the following steps:
步骤S102b1:按照预设处理时间,采用等离子体对图10中外延层20的表面进行处理,如图17所示。也就是说,得到图10所示的结构后,可以不对外延层20进行刻蚀,直接对外延层20的表面进行处理。Step S102b1: Use plasma to process the surface of the epitaxial layer 20 in Figure 10 according to the preset processing time, as shown in Figure 17. That is to say, after obtaining the structure shown in FIG. 10 , the epitaxial layer 20 may not be etched, but the surface of the epitaxial layer 20 may be directly processed.
需要说明的是,预设处理时间和等离子体的相关介绍可参考上文,本申请实施例不再赘述。It should be noted that the related introduction of the preset processing time and plasma can be referred to the above, and will not be described again in the embodiments of the present application.
步骤S102b2:根据掩膜层70,在外延层20(可以是盖帽层23)的表面形成掺杂层30,如图18所示。Step S102b2: According to the mask layer 70, form the doped layer 30 on the surface of the epitaxial layer 20 (which may be the cap layer 23), as shown in FIG. 18.
通过对比可以发现,图12所示的实施例中,根据掩膜层70对部分外延层20进行刻蚀形成凹槽A,对凹槽A进行处理,进一步在凹槽A内部形成掺杂层30。而图16所示的实施例中,未对部分外延层20进行刻蚀,而是直接对外延层20的表面进行处理,并根据掩膜层70在外延层20的表面形成掺杂层30。Through comparison, it can be found that in the embodiment shown in FIG. 12 , part of the epitaxial layer 20 is etched according to the mask layer 70 to form the groove A, and the groove A is processed to further form the doping layer 30 inside the groove A. . In the embodiment shown in FIG. 16 , part of the epitaxial layer 20 is not etched, but the surface of the epitaxial layer 20 is directly processed, and the doping layer 30 is formed on the surface of the epitaxial layer 20 according to the mask layer 70 .
步骤S103:在掺杂层30的表面形成电极层50,按照预设退火温度对电极层50进行退火。Step S103: Form an electrode layer 50 on the surface of the doped layer 30, and anneal the electrode layer 50 according to a preset annealing temperature.
在本申请的一种可能实现的方式中,如图19所示,可以在图15中掺杂层30的表面形成电极层50(包括源极层51和漏极层52)。去除掩膜层70,如图20所示。按照预设退火温度对电极层50进行退火,进而不仅可以实现电极层50与外延层20的欧姆接触,而且通过掺杂层30可以降低欧姆接触的接触电阻率。In a possible implementation manner of the present application, as shown in FIG. 19 , an electrode layer 50 (including a source layer 51 and a drain layer 52 ) can be formed on the surface of the doped layer 30 in FIG. 15 . Mask layer 70 is removed, as shown in Figure 20. Annealing the electrode layer 50 according to the preset annealing temperature can not only achieve ohmic contact between the electrode layer 50 and the epitaxial layer 20 , but also reduce the contact resistivity of the ohmic contact through the doping layer 30 .
在本申请的另一种可能实现的方式中,可以在图18中掺杂层30的表面形成电极层50(包括源极 层51和漏极层52)。去除掩膜层70,如图21所示。按照预设退火温度对电极层50进行退火,同样可以实现电极层50与外延层20的欧姆接触,而且通过掺杂层30可以降低欧姆接触的接触电阻率。In another possible implementation manner of the present application, the electrode layer 50 (including the source electrode) can be formed on the surface of the doped layer 30 in FIG. 18 layer 51 and drain layer 52). Mask layer 70 is removed, as shown in Figure 21. Annealing the electrode layer 50 according to the preset annealing temperature can also achieve ohmic contact between the electrode layer 50 and the epitaxial layer 20 , and the contact resistivity of the ohmic contact can be reduced through the doping layer 30 .
上述两种可能实现的方式中,掺杂层30的材料、状态和厚度等可以参考上文介绍,本申请实施例在此不再赘述。Among the above two possible implementation methods, the material, state and thickness of the doping layer 30 can be referred to the above introduction, and will not be described again in the embodiment of the present application.
可选地,可以以400℃~800℃的预设退火温度,采用退火炉等退火设备或激光对源极层51和漏极层52进行退火,对退火设备的性能要求低,实现相对较低温度的退火,不仅降低了退火成本,且与后续栅极层60的制备工艺兼容。Alternatively, the source layer 51 and the drain layer 52 can be annealed using annealing equipment such as an annealing furnace or laser at a preset annealing temperature of 400°C to 800°C. The performance requirements for the annealing equipment are low and the implementation is relatively low. Temperature annealing not only reduces the annealing cost, but is also compatible with the subsequent preparation process of the gate layer 60 .
进一步地,上述两种可能实现的方式可以采用上述沉积工艺中的任意一项在盖帽层23的表面沉积金属,并通过剥离工艺或者干法刻蚀工艺等将掩膜层70表面的金属去除,形成源极层51和漏极层52。其中,剥离工艺是指盖帽层23经过涂覆光致抗蚀剂、曝光、显影后,以具有一定图形的光致抗蚀剂为掩模,蒸发沉积的金属,然后在去除光致抗蚀剂的同时,剥离掩膜上沉积的金属,即可形成源极层51和漏极层52。干法刻蚀工艺是指利用反应气体与等离子体对沉积的金属进行刻蚀。本申请实施例中,可以采用反应离子刻蚀工艺去除掩膜层70表面的金属,形成源极层51和漏极层52。Further, the above two possible implementation methods can use any one of the above deposition processes to deposit metal on the surface of the cap layer 23, and remove the metal on the surface of the mask layer 70 through a stripping process or a dry etching process. Source layer 51 and drain layer 52 are formed. The stripping process refers to that after the capping layer 23 is coated with photoresist, exposed, and developed, the deposited metal is evaporated using a photoresist with a certain pattern as a mask, and then the photoresist is removed. At the same time, the metal deposited on the mask is peeled off to form the source layer 51 and the drain layer 52 . The dry etching process refers to the use of reactive gases and plasma to etch deposited metal. In this embodiment of the present application, a reactive ion etching process may be used to remove metal on the surface of the mask layer 70 to form the source layer 51 and the drain layer 52 .
本申请实施例中,采用EBE工艺在掺杂层30的表面依次沉积Ti、Al、Ti、Au,形成源极层51和漏极层52。其中,Ti、Al、Ti、Au的厚度对应为20nm、150nm、30nm、50nm。In the embodiment of the present application, the EBE process is used to sequentially deposit Ti, Al, Ti, and Au on the surface of the doped layer 30 to form the source layer 51 and the drain layer 52 . Among them, the thicknesses of Ti, Al, Ti, and Au correspond to 20nm, 150nm, 30nm, and 50nm.
在本申请的一些实施例中,如图22所示,本申请实施例在图20或图21的基础上,还可以通过以下步骤形成栅极层60:In some embodiments of the present application, as shown in Figure 22, based on Figure 20 or Figure 21, the gate layer 60 can also be formed through the following steps:
步骤S104a1:在外延层20(可以是盖帽层23)的表面形成介质层40。Step S104a1: Form the dielectric layer 40 on the surface of the epitaxial layer 20 (which may be the cap layer 23).
需要说明的是,在图20所示的基础上形成介质层40,如图23所示;或者还可以在图21所示的基础上形成介质层40,此处不再赘述。It should be noted that the dielectric layer 40 can be formed on the basis of what is shown in Figure 20, as shown in Figure 23; or the dielectric layer 40 can also be formed on the basis of what is shown in Figure 21, which will not be described again here.
步骤S104a2:对介质层40进行光刻和刻蚀,形成凹槽B。Step S104a2: Perform photolithography and etching on the dielectric layer 40 to form the groove B.
例如,在图23所示的介质层40的基础上,形成凹槽B,如图24所示。For example, on the basis of the dielectric layer 40 shown in FIG. 23, a groove B is formed, as shown in FIG. 24.
步骤S104a3:在凹槽B内部形成栅极层60。Step S104a3: Form the gate layer 60 inside the groove B.
例如,在图24所示的基础上形成栅极层60,如图1所示。For example, the gate layer 60 is formed on the basis shown in FIG. 24 , as shown in FIG. 1 .
综上所述,本申请实施例提供半导体器件1的制备方法可以通过图25或图26实现,下面详细介绍步骤。In summary, the method for manufacturing the semiconductor device 1 provided by the embodiment of the present application can be implemented through FIG. 25 or FIG. 26 , and the steps are described in detail below.
如图25所示,制备过程200可以通过以下步骤实现:As shown in Figure 25, the preparation process 200 can be implemented through the following steps:
步骤S201:对外延层20进行光刻,形成掩膜层70,如图10所示。Step S201: Perform photolithography on the epitaxial layer 20 to form a mask layer 70, as shown in FIG. 10 .
步骤S202:根据掩膜层70对部分外延层20进行刻蚀,形成凹槽A,如图13所示。Step S202: Etch part of the epitaxial layer 20 according to the mask layer 70 to form a groove A, as shown in FIG. 13 .
步骤S203:采用等离子体对凹槽A进行处理,如图14所示。Step S203: Use plasma to process groove A, as shown in Figure 14.
步骤S204:在凹槽A内部形成掺杂层30,如图15所示。Step S204: Form the doping layer 30 inside the groove A, as shown in FIG. 15 .
步骤S205:在掺杂层30的表面形成电极层50,如图19所示。Step S205: Form an electrode layer 50 on the surface of the doped layer 30, as shown in Figure 19.
步骤S206:去除掩膜层70,如图20所示。Step S206: Remove the mask layer 70, as shown in Figure 20.
步骤S207:按照预设退火温度对电极层50进行退火。Step S207: Anneal the electrode layer 50 according to the preset annealing temperature.
步骤S208:在外延层20的表面形成介质层40,如图23所示。Step S208: Form a dielectric layer 40 on the surface of the epitaxial layer 20, as shown in FIG. 23.
步骤S209:对介质层40进行光刻和刻蚀,形成凹槽B。Step S209: Perform photolithography and etching on the dielectric layer 40 to form groove B.
步骤S210:在凹槽B内部形成栅极层60,如图1所示。Step S210: Form the gate layer 60 inside the groove B, as shown in FIG. 1 .
需要说明的是,上述步骤S201至步骤S210的详细过程可以参考上文介绍,本申请实施例不再赘述。It should be noted that the detailed process from step S201 to step S210 can be referred to the above introduction, and will not be described again in the embodiment of the present application.
如图26所示,制备过程300可以通过以下步骤实现:As shown in Figure 26, the preparation process 300 can be implemented through the following steps:
步骤S301:对外延层20进行光刻,形成掩膜层70,如图10所示。Step S301: Perform photolithography on the epitaxial layer 20 to form a mask layer 70, as shown in FIG. 10 .
步骤S302:采用等离子体对外延层20进行处理,如图17所示。Step S302: Use plasma to process the epitaxial layer 20, as shown in Figure 17.
步骤S303:根据掩膜层70,在外延层20的表面形成掺杂层30,如图18所示。Step S303: According to the mask layer 70, form the doping layer 30 on the surface of the epitaxial layer 20, as shown in FIG. 18.
步骤S304:在掺杂层70的表面形成电极层50。Step S304: Form the electrode layer 50 on the surface of the doped layer 70.
步骤S305:去除掩膜层70,如图21所示。Step S305: Remove the mask layer 70, as shown in Figure 21.
步骤S306:按照预设退火温度对电极层50进行退火。Step S306: Anneal the electrode layer 50 according to the preset annealing temperature.
步骤S307:在外延层20的表面形成介质层40。Step S307: Form the dielectric layer 40 on the surface of the epitaxial layer 20.
步骤S308:对介质层40进行光刻和刻蚀,形成凹槽B。 Step S308: Perform photolithography and etching on the dielectric layer 40 to form the groove B.
步骤S309:在凹槽B内部形成栅极层60。Step S309: Form the gate layer 60 inside the groove B.
需要说明的是,上述步骤S301至步骤S309的详细过程可以参考上文介绍,本申请实施例不再赘述。It should be noted that the detailed process from step S301 to step S309 can be referred to the above introduction, and will not be described again in the embodiment of the present application.
通过对比可以发现,制备过程200中,对部分外延层20进行刻蚀,之后形成掺杂层30、电极层50、介质层40和栅极层60的。而制备过程300中,仅对外延层20进行光刻,之后形成掺杂层30、电极层50、介质层40和栅极层60。Through comparison, it can be found that in the preparation process 200, part of the epitaxial layer 20 is etched, and then the doped layer 30, the electrode layer 50, the dielectric layer 40 and the gate layer 60 are formed. In the preparation process 300 , only the epitaxial layer 20 is photolithographed, and then the doping layer 30 , the electrode layer 50 , the dielectric layer 40 and the gate layer 60 are formed.
本申请实施例提供了另一种半导体器件1的制备方法,如图27所示,制备过程400可以按照如下步骤实现:The embodiment of the present application provides another method of preparing a semiconductor device 1. As shown in Figure 27, the preparation process 400 can be implemented according to the following steps:
步骤S401:对介质层40进行光刻,形成掩膜层70。Step S401: Perform photolithography on the dielectric layer 40 to form a mask layer 70.
可选地,在对介质层40进行光刻前,可以在外延层20的表面形成介质层40,如图28所示。Optionally, before photolithography is performed on the dielectric layer 40, the dielectric layer 40 may be formed on the surface of the epitaxial layer 20, as shown in FIG. 28.
进一步地,参考图29,步骤S101中对介质层40进行光刻形成掩膜层70(如图30所示)可以进一步按照如下步骤实现:Further, referring to Figure 29, in step S101, photolithography is performed on the dielectric layer 40 to form the mask layer 70 (as shown in Figure 30), which can be further implemented as follows:
步骤S401a1:在介质层40表面涂光刻胶,并按照预设烘烤温度和预设烘烤时间对涂有光刻胶的介质层40进行烘烤。Step S401a1: Coat photoresist on the surface of the dielectric layer 40, and bake the dielectric layer 40 coated with photoresist according to the preset baking temperature and preset baking time.
可选地,可以以90℃~120℃的预设烘烤温度和60s~120s的预设烘烤时间对涂有光刻胶的介质层40进行烘烤,使液态的光刻胶在介质层40表面固化。当然,还可以为其他烘烤温度和其他烘烤时间对涂有光刻胶的介质层40进行烘烤,本申请实施例不做限定。Optionally, the dielectric layer 40 coated with photoresist can be baked at a preset baking temperature of 90°C to 120°C and a preset baking time of 60s to 120s, so that the liquid photoresist is on the surface of the dielectric layer 40 solidify. Of course, the dielectric layer 40 coated with photoresist can also be baked at other baking temperatures and other baking times, which are not limited by the embodiments of the present application.
本申请实施例中,可以在介质层40的表面涂光刻胶Az5214,在90℃的烘烤温度下对涂有光刻胶的介质层40烘烤90s。In the embodiment of the present application, photoresist Az5214 can be coated on the surface of the dielectric layer 40, and the dielectric layer 40 coated with the photoresist is baked at a baking temperature of 90°C for 90 seconds.
步骤S401a2:按照预设曝光时间,对烘烤后的介质层40进行曝光。Step S401a2: Expose the baked dielectric layer 40 according to the preset exposure time.
类似的,可以以100ms~1000ms的预设曝光时间对烘烤后的介质层40进行曝光,能够将掩模版上的图形转移转移到固化后的光刻胶上。当然,预设曝光时间还可以为其他时间范围,本申请实施例不做限定。Similarly, the baked dielectric layer 40 can be exposed with a preset exposure time of 100 ms to 1000 ms, so that the pattern on the mask can be transferred to the cured photoresist. Of course, the preset exposure time can also be in other time ranges, which is not limited in the embodiments of this application.
本申请实施例中,可以对烘烤后的介质层40曝光200ms。In the embodiment of the present application, the baked dielectric layer 40 may be exposed for 200 ms.
步骤S401a3:采用显影液,并按照预设显影时间对曝光后的介质层40进行显影,形成掩膜层70,如图30所示。Step S401a3: Use a developer to develop the exposed dielectric layer 40 according to a preset development time to form a mask layer 70, as shown in FIG. 30 .
类似的,可以采用TMAH溶液,以30s~90s的预设显影时间对曝光后的介质层40进行显影,可以将固化后的光刻胶上的图形转移至介质层40上。当然,显影液还可以为其他溶液,预设显影时间还可以为其他时间范围,本申请实施例不做限定。Similarly, a TMAH solution can be used to develop the exposed dielectric layer 40 with a preset development time of 30 to 90 seconds, and the pattern on the cured photoresist can be transferred to the dielectric layer 40 . Of course, the developing solution can also be other solutions, and the preset development time can also be other time ranges, which are not limited in the embodiments of this application.
在本申请实施例中,可以采用TMAH溶液对曝光后的介质层40显影50s,形成厚度为1um的掩膜层70。In the embodiment of the present application, a TMAH solution can be used to develop the exposed dielectric layer 40 for 50 seconds to form a mask layer 70 with a thickness of 1 μm.
步骤S402:根据掩膜层70形成掺杂层30,可以分为以下几种实施例进行介绍:Step S402: Forming the doping layer 30 according to the mask layer 70, which can be divided into the following embodiments for introduction:
在本申请的一些实施例中,可以按照以下步骤形成掺杂层30:In some embodiments of the present application, the doped layer 30 may be formed according to the following steps:
步骤S402a1:根据图30的掩膜层70对介质层40和部分外延层20进行刻蚀,形成凹槽A,如图31所示。Step S402a1: Etch the dielectric layer 40 and part of the epitaxial layer 20 according to the mask layer 70 in Figure 30 to form a groove A, as shown in Figure 31 .
步骤S402a2:去除掩膜层70,如图32所示。Step S402a2: Remove the mask layer 70, as shown in Figure 32.
步骤S402a3:按照预设处理时间,采用等离子体对凹槽A进行处理,如图33所示。Step S402a3: Use plasma to process groove A according to the preset processing time, as shown in Figure 33.
需要说明的是,预设处理时间和等离子体的介绍可以参考前文介绍,本申请实施例不再赘述。It should be noted that the introduction of the preset processing time and plasma can be referred to the previous introduction, and will not be described again in the embodiments of this application.
本申请实施例中,可以采用Ar对凹槽A处理10min,不仅能够增大凹槽A的表面粗糙度,还可以增加凹槽A表面的N空位,进一步降低电极层50与外延层20的欧姆接触的接触电阻率。In the embodiment of the present application, Ar can be used to treat groove A for 10 minutes, which can not only increase the surface roughness of groove A, but also increase the N vacancies on the surface of groove A, further reducing the ohmic resistance of the electrode layer 50 and the epitaxial layer 20 Contact resistivity of the contact.
步骤S402a4:采用沉积工艺在凹槽A内部形成掺杂层30,如图34所示。Step S402a4: Use a deposition process to form the doping layer 30 inside the groove A, as shown in Figure 34.
需要说明的是,掺杂层30的材料、状态和厚度以及沉积工艺等可以参考上文介绍,本申请实施例不再赘述。It should be noted that the material, state, thickness and deposition process of the doping layer 30 can be referred to the above introduction, and will not be described again in the embodiment of the present application.
本申请实施例中,采用PECVD工艺在凹槽A内部沉积多晶硅,形成厚度为5nm的掺杂层30。In the embodiment of the present application, a PECVD process is used to deposit polysilicon inside the groove A to form a doped layer 30 with a thickness of 5 nm.
在本申请的另一些实施例中,可以按照以下步骤形成掺杂层30:In other embodiments of the present application, the doping layer 30 may be formed according to the following steps:
步骤S402b1:根据图30的掩膜层70对介质层40进行刻蚀,形成凹槽A,如图35所示。Step S402b1: Etch the dielectric layer 40 according to the mask layer 70 in Figure 30 to form a groove A, as shown in Figure 35 .
步骤S402b2:去除掩膜层70。Step S402b2: Remove the mask layer 70.
步骤S402b3:按照预设处理时间,采用等离子体对凹槽A进行处理。 Step S402b3: Use plasma to process groove A according to the preset processing time.
需要说明的是,预设处理时间和等离子体的介绍可以参考前文介绍,本申请实施例不再赘述。It should be noted that the introduction of the preset processing time and plasma can be referred to the previous introduction, and will not be described again in the embodiments of this application.
本申请实施例中,可以采用Ar对凹槽A处理10min,不仅能够增大凹槽A的表面粗糙度,还可以增加凹槽A表面的N空位,进一步降低电极层50与外延层20的欧姆接触的接触电阻率。In the embodiment of the present application, Ar can be used to treat groove A for 10 minutes, which can not only increase the surface roughness of groove A, but also increase the N vacancies on the surface of groove A, further reducing the ohmic resistance of the electrode layer 50 and the epitaxial layer 20 Contact resistivity of the contact.
步骤S402b4:采用沉积工艺在凹槽A内部形成掺杂层30,如图36所示。Step S402b4: Use a deposition process to form the doping layer 30 inside the groove A, as shown in Figure 36.
需要说明的是,掺杂层30的材料、状态和厚度以及沉积工艺等可以参考上文介绍,本申请实施例不再赘述。It should be noted that the material, state, thickness and deposition process of the doping layer 30 can be referred to the above introduction, and will not be described again in the embodiment of the present application.
本申请实施例中,采用PECVD工艺在凹槽A内部沉积多晶硅,形成厚度为5nm的掺杂层30。In the embodiment of the present application, a PECVD process is used to deposit polysilicon inside the groove A to form a doped layer 30 with a thickness of 5 nm.
通过对比可以发现,步骤S402a1至步骤S402a4的实施例中,根据掩膜层70对介质层40和部分外延层20进行刻蚀形成凹槽A,对凹槽A进行处理,进一步在凹槽A内部形成掺杂层30。而步骤S402b1至步骤S402b4的实施例中,根据掩膜层70对仅介质层40进行刻蚀形成凹槽A,对凹槽A进行处理,进一步在凹槽A内部形成掺杂层30。Through comparison, it can be found that in the embodiment from step S402a1 to step S402a4, the dielectric layer 40 and part of the epitaxial layer 20 are etched according to the mask layer 70 to form the groove A, the groove A is processed, and further inside the groove A Doped layer 30 is formed. In the embodiment of steps S402b1 to S402b4, only the dielectric layer 40 is etched according to the mask layer 70 to form the groove A, the groove A is processed, and the doping layer 30 is further formed inside the groove A.
步骤S403:在掺杂层30的表面形成电极层50,按照预设退火温度对电极层50进行退火。Step S403: Form an electrode layer 50 on the surface of the doped layer 30, and anneal the electrode layer 50 according to a preset annealing temperature.
在本申请的一种可能实现的方式中,可以在图34中掺杂层30的表面形成电极层50(也就是形成源极层51和漏极层52),如图23所示。按照预设退火温度对电极层50进行退火,进而不仅可以实现电极层50与外延层20的欧姆接触,而且通过掺杂层30可以降低欧姆接触的接触电阻率。In a possible implementation manner of the present application, the electrode layer 50 (that is, the source layer 51 and the drain layer 52 are formed) can be formed on the surface of the doped layer 30 in FIG. 34 , as shown in FIG. 23 . Annealing the electrode layer 50 according to the preset annealing temperature can not only achieve ohmic contact between the electrode layer 50 and the epitaxial layer 20 , but also reduce the contact resistivity of the ohmic contact through the doping layer 30 .
在本申请的另一种可能实现的方式中,可以在图36中掺杂层30的表面形成电极层50(也就是形成源极层51和漏极层52)。按照预设退火温度对电极层50进行退火,同样可以实现电极层50与外延层20的欧姆接触,而且通过掺杂层30可以降低欧姆接触的接触电阻率。In another possible implementation manner of the present application, the electrode layer 50 (that is, the source layer 51 and the drain layer 52 are formed) can be formed on the surface of the doped layer 30 in FIG. 36 . Annealing the electrode layer 50 according to the preset annealing temperature can also achieve ohmic contact between the electrode layer 50 and the epitaxial layer 20 , and the contact resistivity of the ohmic contact can be reduced through the doping layer 30 .
上述两种可能实现的方式中,掺杂层30的材料、状态和厚度等可以参考上文介绍,本申请实施例在此不再赘述。Among the above two possible implementation methods, the material, state and thickness of the doping layer 30 can be referred to the above introduction, and will not be described again in the embodiment of the present application.
可选地,可以以400℃~800℃的预设退火温度,采用退火炉等退火设备或激光对源极层51和漏极层52进行退火,对退火设备的性能要求低,实现相对较低温度的退火,不仅降低了退火成本,且与后续栅极层60的制备工艺兼容。Alternatively, the source layer 51 and the drain layer 52 can be annealed using annealing equipment such as an annealing furnace or laser at a preset annealing temperature of 400°C to 800°C. The performance requirements for the annealing equipment are low and the implementation is relatively low. Temperature annealing not only reduces the annealing cost, but is also compatible with the subsequent preparation process of the gate layer 60 .
进一步的,上述两种可能实现的方式可以采用上述沉积工艺中的任意一项在盖帽层23的表面沉积金属,并通过剥离工艺或者刻蚀工艺等将掩膜层70表面的金属去除,形成源极层51和漏极层52。Furthermore, the above two possible implementation methods can use any one of the above deposition processes to deposit metal on the surface of the cap layer 23, and remove the metal on the surface of the mask layer 70 through a stripping process or an etching process to form a source. electrode layer 51 and drain layer 52.
本申请实施例中,采用EBE工艺在掺杂层30的表面依次沉积Ti、Al、Ti、Au,形成源极层51和漏极层52。其中,Ti、Al、Ti、Au的厚度对应为20nm、150nm、30nm、50nm。In the embodiment of the present application, the EBE process is used to sequentially deposit Ti, Al, Ti, and Au on the surface of the doped layer 30 to form the source layer 51 and the drain layer 52 . Among them, the thicknesses of Ti, Al, Ti, and Au correspond to 20nm, 150nm, 30nm, and 50nm.
在本申请的一些实施例中,本申请实施例在图23的基础上,还可以通过以下步骤形成栅极层60:In some embodiments of the present application, on the basis of Figure 23, the gate layer 60 can also be formed through the following steps:
步骤S404a1:对介质层40进行光刻和刻蚀,形成凹槽B。Step S404a1: Perform photolithography and etching on the dielectric layer 40 to form groove B.
例如,在图23所示的基础上形成凹槽B,如图24所示。For example, groove B is formed on the basis shown in Fig. 23, as shown in Fig. 24.
步骤S404a2:在凹槽B内部形成栅极层60。Step S404a2: Form the gate layer 60 inside the groove B.
例如,在图24所示的基础上形成栅极层60,如图1所示。For example, the gate layer 60 is formed on the basis shown in FIG. 24 , as shown in FIG. 1 .
综上所述,本申请实施例提供半导体器件1的制备方法可以通过图37实现,下面详细介绍步骤。In summary, the method for manufacturing the semiconductor device 1 provided by the embodiment of the present application can be implemented through FIG. 37 , and the steps are described in detail below.
如图37所示,制备过程500可以通过以下步骤实现:As shown in Figure 37, the preparation process 500 can be implemented through the following steps:
步骤S501:在外延层20表面形成介质层40,如图28所示。Step S501: Form a dielectric layer 40 on the surface of the epitaxial layer 20, as shown in Figure 28.
步骤S502:对介质层40进行光刻,形成掩膜层70,如图30所示。Step S502: Perform photolithography on the dielectric layer 40 to form a mask layer 70, as shown in FIG. 30 .
步骤S503:根据掩膜层70对介质层40和部分外延层20进行刻蚀,形成凹槽A。或者,根据掩膜层70对介质层40进行刻蚀,形成凹槽A。Step S503: Etch the dielectric layer 40 and part of the epitaxial layer 20 according to the mask layer 70 to form a groove A. Alternatively, the dielectric layer 40 is etched according to the mask layer 70 to form the groove A.
需要说明的是,若对介质层40和部分外延层2进行刻蚀,形成的凹槽A如图31所示。若对介质层40进行刻蚀,形成的凹槽A如图35所示。It should be noted that if the dielectric layer 40 and part of the epitaxial layer 2 are etched, the groove A formed is as shown in FIG. 31 . If the dielectric layer 40 is etched, the groove A formed is as shown in FIG. 35 .
步骤S504:去除掩膜层70,如图32所示。Step S504: Remove the mask layer 70, as shown in Figure 32.
步骤S505:采用等离子体对凹槽A进行处理,如图33所示。Step S505: Use plasma to process groove A, as shown in Figure 33.
步骤S506:在凹槽A内部形成掺杂层30,如图34或图36所示。Step S506: Form the doping layer 30 inside the groove A, as shown in Figure 34 or Figure 36.
步骤S507:在掺杂层30的表面形成电极层50,如图23所示。Step S507: Form an electrode layer 50 on the surface of the doped layer 30, as shown in FIG. 23.
步骤S508:按照预设退火温度对电极层50进行退火。Step S508: Anneal the electrode layer 50 according to the preset annealing temperature.
步骤S509:对介质层40进行光刻和刻蚀,形成凹槽B。Step S509: Perform photolithography and etching on the dielectric layer 40 to form groove B.
步骤S510:在凹槽B内部形成栅极层60,如图1所示。Step S510: Form the gate layer 60 inside the groove B, as shown in FIG. 1 .
需要说明的是,上述步骤S501至步骤S510的详细过程可以参考上文介绍,本申请实施例不再赘 述。It should be noted that the detailed process from step S501 to step S510 can be referred to the above introduction, and will not be repeated in the embodiment of this application. narrate.
应理解,在本申请的各种实施例中,上述各过程的序号的大小并不意味着执行顺序的先后,各过程的执行顺序应以其功能和内在逻辑确定,而不应对本申请实施例的实施过程构成任何限定。It should be understood that in the various embodiments of the present application, the size of the sequence numbers of the above-mentioned processes does not mean the order of execution. The execution order of each process should be determined by its functions and internal logic, and should not be used in the embodiments of the present application. The implementation process constitutes any limitation.
本申请实施例提供了一种电子芯片,可以包括无源器件和半导体器件1。其中,无源器件可以与半导体器件1电连接。The embodiment of the present application provides an electronic chip, which may include passive devices and semiconductor devices 1 . Among them, the passive device may be electrically connected to the semiconductor device 1 .
可选地,无源器件可以为电阻、电容等。当然,无源器件还可以为其他器件,本申请实施例不做限定。Optionally, passive components may be resistors, capacitors, etc. Of course, the passive components can also be other components, which are not limited in the embodiments of this application.
本申请实施例提供了一种电子设备,可以包括电路板和上述电子芯片。其中,电子芯片可以设置在电路板上。An embodiment of the present application provides an electronic device, which may include a circuit board and the above-mentioned electronic chip. Among them, the electronic chip can be arranged on the circuit board.
以上所述,仅为本申请的具体实施方式,但本申请的保护范围并不局限于此,任何熟悉本技术领域的技术人员在本申请揭露的技术范围内,可轻易想到变化或替换,都应涵盖在本申请的保护范围之内。因此,本申请的保护范围应所述以权利要求的保护范围为准。 The above are only specific embodiments of the present application, but the protection scope of the present application is not limited thereto. Any person familiar with the technical field can easily think of changes or substitutions within the technical scope disclosed in the present application. should be covered by the protection scope of this application. Therefore, the protection scope of this application should be determined by the protection scope of the claims.

Claims (20)

  1. 一种半导体器件,其特征在于,包括外延层、掺杂层、介质层和第一电极层;A semiconductor device, characterized by including an epitaxial layer, a doping layer, a dielectric layer and a first electrode layer;
    所述外延层和所述介质层层叠设置,所述半导体器件设有第一凹槽,所述掺杂层和所述第一电极层的一部分层叠设置于所述第一凹槽内部。The epitaxial layer and the dielectric layer are stacked and arranged, the semiconductor device is provided with a first groove, and the doped layer and a part of the first electrode layer are stacked and arranged inside the first groove.
  2. 根据权利要求1所述的半导体器件,其特征在于,所述掺杂层的材料为硅、氧化硅、氮化硅和氮氧化硅中的一种或多种;The semiconductor device according to claim 1, wherein the material of the doped layer is one or more of silicon, silicon oxide, silicon nitride and silicon oxynitride;
    所述掺杂层的状态为单晶状态、多晶状态或非晶状态;The state of the doped layer is a single crystal state, a polycrystalline state or an amorphous state;
    所述掺杂层的厚度为1nm~50nm。The thickness of the doped layer is 1 nm to 50 nm.
  3. 根据权利要求2所述的半导体器件,其特征在于,所述掺杂层从硅的峰值浓度降到硅浓度为10%的厚度小于20nm。The semiconductor device according to claim 2, wherein the thickness of the doped layer is less than 20 nm when the peak concentration of silicon is reduced to a silicon concentration of 10%.
  4. 根据权利要求2所述的半导体器件,其特征在于,所述掺杂层从硅的第一浓度降到硅浓度为10%的厚度小于20nm;The semiconductor device according to claim 2, wherein the thickness of the doped layer from the first concentration of silicon to the silicon concentration of 10% is less than 20 nm;
    其中,所述第一浓度大于或等于60%。Wherein, the first concentration is greater than or equal to 60%.
  5. 根据权利要求1至4中任一项所述的半导体器件,其特征在于,所述掺杂层、所述外延层和所述第一电极层均不同。The semiconductor device according to any one of claims 1 to 4, wherein the doped layer, the epitaxial layer and the first electrode layer are all different.
  6. 根据权利要求1至5中任一项所述的半导体器件,其特征在于,所述外延层包括层叠设置于衬底表面的沟道层、势垒层和盖帽层;The semiconductor device according to any one of claims 1 to 5, wherein the epitaxial layer includes a channel layer, a barrier layer and a cap layer that are stacked on the surface of the substrate;
    所述第一凹槽的底部位于所述盖帽层、所述势垒层或所述沟道层。The bottom of the first groove is located on the cap layer, the barrier layer or the channel layer.
  7. 根据权利要求6所述的半导体器件,其特征在于,所述第一凹槽的底部与所述沟道层的表面距离20nm以内;所述沟道层的表面用于指示所述沟道层靠近所述势垒层的表面。The semiconductor device according to claim 6, wherein the distance between the bottom of the first groove and the surface of the channel layer is within 20 nm; the surface of the channel layer is used to indicate that the channel layer is close to The surface of the barrier layer.
  8. 根据权利要求6或7所述的半导体器件,其特征在于,所述介质层设有第二凹槽,所述第二凹槽的底部位于所述盖帽层的表面;所述盖帽层的表面用于指示所述盖帽层背离所述势垒层的表面;The semiconductor device according to claim 6 or 7, characterized in that the dielectric layer is provided with a second groove, the bottom of the second groove is located on the surface of the capping layer; the surface of the capping layer is Indicating the surface of the capping layer facing away from the barrier layer;
    所述半导体器件还包括第二电极层,所述第二电极层的一部分位于所述第二凹槽内部。The semiconductor device further includes a second electrode layer, a portion of which is located inside the second groove.
  9. 根据权利要求8所述的半导体器件,其特征在于,所述第一电极层的材料包括钛Ti、金Au和铝Al中的一种或多种;The semiconductor device according to claim 8, wherein the material of the first electrode layer includes one or more of titanium Ti, gold Au and aluminum Al;
    所述第二电极层的材料包括所述钛Ti、所述金Au和镍Ni中的一种或多种。The material of the second electrode layer includes one or more of the titanium Ti, the gold Au, and nickel Ni.
  10. 一种半导体器件的制备方法,其特征在于,包括:A method for preparing a semiconductor device, characterized in that it includes:
    对外延层或介质层进行光刻,形成掩膜层;Perform photolithography on the epitaxial layer or dielectric layer to form a mask layer;
    根据所述掩膜层形成掺杂层;Form a doping layer according to the mask layer;
    在所述掺杂层的表面形成第一电极层,按照预设退火温度对所述第一电极层进行退火。A first electrode layer is formed on the surface of the doped layer, and the first electrode layer is annealed according to a preset annealing temperature.
  11. 根据权利要求10所述的制备方法,其特征在于,所述根据所述掩膜层形成掺杂层,包括:The preparation method according to claim 10, characterized in that forming the doping layer according to the mask layer includes:
    根据所述掩膜层,在所述外延层的表面形成所述掺杂层。According to the mask layer, the doped layer is formed on the surface of the epitaxial layer.
  12. 根据权利要求11所述的制备方法,其特征在于,所述制备方法还包括:The preparation method according to claim 11, characterized in that the preparation method further includes:
    按照预设处理时间,采用等离子体对所述外延层的表面进行处理,According to the preset processing time, the surface of the epitaxial layer is treated with plasma,
    其中,所述预设处理时间为2min~60min;Wherein, the preset processing time is 2min~60min;
    所述等离子体包括氢气H2、氮气N2、氨气NH3、氯气Cl2、氩气Ar和氧气O2中的一种或多种。The plasma includes one or more of hydrogen H 2 , nitrogen N 2 , ammonia NH 3 , chlorine Cl 2 , argon Ar and oxygen O 2 .
  13. 根据权利要求10所述的制备方法,其特征在于,所述根据所述掩膜层形成掺杂层,包括:The preparation method according to claim 10, characterized in that forming the doping layer according to the mask layer includes:
    根据所述掩膜层对部分所述外延层进行刻蚀,形成第一凹槽;Etch part of the epitaxial layer according to the mask layer to form a first groove;
    采用沉积工艺在所述第一凹槽内部形成所述掺杂层。The doping layer is formed inside the first groove using a deposition process.
  14. 根据权利要求10所述的制备方法,其特征在于,所述根据所述掩膜层形成掺杂层,包括:The preparation method according to claim 10, characterized in that forming the doping layer according to the mask layer includes:
    根据所述掩膜层对所述介质层进行刻蚀,形成第一凹槽;或者,根据所述掩膜层对所述介质层和部分所述外延层进行刻蚀,形成第一凹槽;Etching the dielectric layer according to the mask layer to form a first groove; or etching the dielectric layer and part of the epitaxial layer according to the mask layer to form a first groove;
    采用沉积工艺在所述第一凹槽内部形成掺杂层。A deposition process is used to form a doped layer inside the first groove.
  15. 根据权利要求13或14所述的制备方法,其特征在于,所述制备方法还包括:The preparation method according to claim 13 or 14, characterized in that the preparation method further includes:
    按照预设处理时间,采用等离子体对所述第一凹槽进行处理,According to the preset processing time, plasma is used to process the first groove,
    其中,所述预设处理时间为2min~60min;Wherein, the preset processing time is 2min~60min;
    所述等离子体包括氢气H2、氮气N2、氨气NH3、氯气Cl2、氩气Ar和氧气O2中的一种或多种。 The plasma includes one or more of hydrogen H 2 , nitrogen N 2 , ammonia NH 3 , chlorine Cl 2 , argon Ar and oxygen O 2 .
  16. 根据权利要求10至15中任一项所述的制备方法,其特征在于,所述掺杂层的材料为硅、氧化硅或氮化硅;The preparation method according to any one of claims 10 to 15, characterized in that the material of the doped layer is silicon, silicon oxide or silicon nitride;
    所述掺杂层的状态为单晶状态、多晶状态或非晶状态;The state of the doped layer is a single crystal state, a polycrystalline state or an amorphous state;
    所述掺杂层的厚度为1nm~50nm。The thickness of the doped layer is 1 nm to 50 nm.
  17. 根据权利要求16所述的制备方法,其特征在于,所述掺杂层从硅的第一浓度降到硅浓度为10%的厚度小于20nm;The preparation method according to claim 16, wherein the thickness of the doped layer is less than 20 nm when the first concentration of silicon is reduced to a silicon concentration of 10%;
    所述第一浓度大于或等于60%。The first concentration is greater than or equal to 60%.
  18. 根据权利要求10至17中任一项所述的制备方法,其特征在于,所述掺杂层、所述外延层和所述第一电极层均不同。The preparation method according to any one of claims 10 to 17, wherein the doped layer, the epitaxial layer and the first electrode layer are all different.
  19. 一种电子芯片,其特征在于,包括无源器件和与所述无源器件电连接的如权利要求1至9中任一项所述的半导体器件。An electronic chip, characterized in that it includes a passive device and a semiconductor device according to any one of claims 1 to 9 that is electrically connected to the passive device.
  20. 一种电子设备,其特征在于,包括电路板和设置在所述电路板上的如权利要求19所述的电子芯片。 An electronic device, characterized by comprising a circuit board and the electronic chip according to claim 19 provided on the circuit board.
PCT/CN2023/117298 2022-09-13 2023-09-06 Semiconductor device and preparation method therefor WO2024055885A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN202211107921.9A CN117747642A (en) 2022-09-13 2022-09-13 Semiconductor device and method for manufacturing the same
CN202211107921.9 2022-09-13

Publications (1)

Publication Number Publication Date
WO2024055885A1 true WO2024055885A1 (en) 2024-03-21

Family

ID=90249438

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2023/117298 WO2024055885A1 (en) 2022-09-13 2023-09-06 Semiconductor device and preparation method therefor

Country Status (2)

Country Link
CN (1) CN117747642A (en)
WO (1) WO2024055885A1 (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060226442A1 (en) * 2005-04-07 2006-10-12 An-Ping Zhang GaN-based high electron mobility transistor and method for making the same
US20070284653A1 (en) * 2006-06-08 2007-12-13 Hiroaki Ueno Semiconductor device
JP2008118044A (en) * 2006-11-07 2008-05-22 Toshiba Corp Field-effect transistor and method for manufacturing the same
US20080128753A1 (en) * 2006-11-30 2008-06-05 Cree, Inc. Transistors and method for making ohmic contact to transistors

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060226442A1 (en) * 2005-04-07 2006-10-12 An-Ping Zhang GaN-based high electron mobility transistor and method for making the same
US20070284653A1 (en) * 2006-06-08 2007-12-13 Hiroaki Ueno Semiconductor device
JP2008118044A (en) * 2006-11-07 2008-05-22 Toshiba Corp Field-effect transistor and method for manufacturing the same
US20080128753A1 (en) * 2006-11-30 2008-06-05 Cree, Inc. Transistors and method for making ohmic contact to transistors

Also Published As

Publication number Publication date
CN117747642A (en) 2024-03-22

Similar Documents

Publication Publication Date Title
CN101506958B (en) Field effect transistor
EP2246880B1 (en) Semiconductor device fabrication method
US10680094B2 (en) Electronic device including a high electron mobility transistor including a gate electrode
US10566428B2 (en) Method for forming gate structures for group III-V field effect transistors
CN104009074A (en) High electron mobility transistor and method of forming the same
CN103165445A (en) In situ grown gate dielectric and field plate dielectric
CN102881720A (en) Taiwan semiconductor mfg
CN103579328A (en) High electron mobility transistor and manufacturing method thereof
CN103930978B (en) Field-effect transistor and its manufacture method
US10453937B2 (en) Self-limited inner spacer formation for gate-all-around field effect transistors
US9755044B2 (en) Method of manufacturing a transistor with oxidized cap layer
CN108987474A (en) A kind of enhancement type high electron mobility transistor and preparation method thereof
US20200212197A1 (en) Method of manufacturing gate structure for gallium nitride high electron mobility transistor
CN103000516B (en) The method forming semiconductor structure
WO2019033762A1 (en) Transistor, array substrate and manufacturing method therefor, and display device
CN104380445A (en) Electrode structure for nitride semiconductor device, production method therefor, and nitride semiconductor field-effect transistor
JP6147018B2 (en) Enhancement mode GaN HEMT device with gate spacer and method of manufacturing the same
WO2024055885A1 (en) Semiconductor device and preparation method therefor
CN109671775B (en) Process for forming nitride semiconductor device
CN111584628A (en) Enhanced GaN HEMT device and preparation method thereof
EP2942805B1 (en) Semiconductor device and manufacturing method
CN107564964B (en) Groove type MOSFET power device and manufacturing method thereof
JP2015073002A (en) Compound semiconductor device and manufacturing method of the same
CN110828542B (en) Semiconductor device and forming method thereof
CN112820774A (en) GaN device and preparation method thereof

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 23864617

Country of ref document: EP

Kind code of ref document: A1