The present invention relates to power semiconductors, and more particularly to a silicon carbide (SiC) heterojunction normally-off high-electron-mobility transistor (HEMT) and a method for preparing the same.
About Group III-V direct bandgap semiconductor heterojunction HEMTs, significant achievements have been acquired in both research and applications. Particularly, (p)AlGaN/(i)GaN heterojunction normally-off lateral field effect transistors were prepared and investigated for working principles thereof [Y Uemoto, M. Hikita, H. Ueno, et al., IEEE Transactions on Electron Devices, Vol. 54, No. 12 (2007): 3393-3399.]. In such a known HFET, a two-dimensional electron gas (2DEG) channel is formed in virtue of the spontaneous, piezoelectric polarization effects of the AlGaN/GaN heterojunction, and a gate (G) is created through evaporation at the AlGaN side of the AlGaN/GaN heterojunction where a (p) GaN layer has been grown. Since the majority carriers in the (p)GaN layer are holes, this helps increase barrier in the conduction band in the channel below the gate (G). When the gate (G) voltage Vg=0, the 2DEG in the channel below the (p)GaN layer is completely depleted, and the device is in a normally-off state. When Vg increases forward and exceeds the built-in potential (Vbi) of the (p)GaN/(p)AlGaN heterojunction, holes enter the channel form the gate (G) via the (p)GaN layer. Otherwise, electrons enter the gate (G) from the channel via the (p)GaN layer and get suppressed by the (p)GaN/(p)AlGaN heterojunction barrier. For electric neutrality, holes enter the channel from the gate (G) via the (p)GaN layer. Since holes are less mobile, they will be combined with some channel electrons to induce conductivity modulation. Meanwhile, only when equivalent electrons accumulated at the source (S) are attracted by the drain (D) biased by the forward voltage to pass the 2DEG channel with high mobility and a drain (D) current Id is formed consequently, the device can work normally. In the device, a P-type GaN layer is arranged below the gate (G) and holes are injected into the channel, so the consequent conductivity modulation at the channel leads to significantly increased Id while Ig remains small. In addition, with controllable lattice mismatch between (p)GaN and (p)AlGaN inserted below the gate (G), any defect of the gate (G) will not have meaningful impact on transport through the AlGaN/GaN heterojunction channel 2DEG, making current collapse of the HFET ignorable.
A metal-AlGaN/GaN heterojunction two-dimensional electron gas Schottky junction tunneling normally-off lateral field effect transistor has been reported and explained for working principles thereof [H. Chen, L. Yuan, K. J. Chen, Phys. Status Solidi C, Vol. 9, No. 3-4 (2012): 871-874.]. Such a known TJ-FET has a 2DEG channel formed by the spontaneous, piezoelectric polarization effect of the AlGaN/GaN heterojunction. At one end of the channel, an alloy (e.g., TiAu) film is deposited to form a Schottky junction, and an ohmic-contact electrode is formed on the alloy film as the source S. An insulating layer of an oxide (e.g., Al2O3) is deposited on the AlGaN layer, and then a gate of an alloy (e.g., NiAu) is made. This gate G overlaps the underlying Schottky junction, so as to prevent formation of any lateral gap between the gate G and the Schottky junction that prevents the gate G voltage from controlling transport of charges through the Schottky junction. An ohmic contact alloy (e.g., TiAlNiAu) is deposited as a film to form a drain at the other end of the heterojunction 2DEG channel through evaporation. When the gate G voltage Vg<0, the 2DEG in the channel below the gate G is depleted, and the channel is cut off. At this time, the Schottky junction barrier is very high, and the lateral thickness is very large. As charges cannot move from the source S tunneling Schottky barrier to the drain D, the current Id at the drain D is 0. When Vg=0, the 2DEG channel below the gate G is on. However, the high Schottky junction barrier and the large lateral thickness prevent charges from moving from the source S tunneling Schottky barrier to the drain D, so the Id is ignorable. When Vg increases forward to a certain extent, the Schottky junction barrier is very low and the lateral thickness is very small, allowing charges to come to the drain D from the source S tunneling Schottky barrier, and Id is quite high. This TJ-FET uses the forward voltage at the gate G to make the electron-tunneling Schottky barrier at the source S reach the drain D, so as to form Id, thereby implementing enhancement. Since Id is obtained by controlling the electron-tunneling Schottky barrier of the source S to reach the drain D using Vg, the device has a very small specific on resistance Ron-sp. When Vg≤0, Id=0. Therefore, the TJ-FET has a breakdown voltage VB significantly higher than that of the traditional HEMT.
There has not been a SiC heterojunction HEMT reported. SiC semiconductors feature stable chemical properties, wide bandgaps, high thermal conductivity, high critical breakdown electric field intensity, high carrier saturated drift velocity, and good resistance against radiation and corrosion. SiC is present in more than 100 different crystal structures, such as 3C—SiC, 4H—SiC, 6H—SiC, and so on. A 3C—SiC cell has four C—Si equivalent bonds, while a 4H—SiC or 6H—SiC cell has one preferential bond (with its direction defined as the c axis) and the other bonds in different directions are not equivalent, so as to cause spontaneous polarization. Additionally, heterojunctions (e.g., 3C/(4, 6) h-SiC, (4, 6) h/3C/(4, 6) h-SiC, etc.) formed by SiC materials different in band gap (Eg), in crystal form, or in crystal plane atom may be used to achieve desired transport of charger carriers and photons. In SiC materials having different crystal forms, lattice constant and thermal conductivity are relatively consistent in directions a and b, so the piezoelectric polarization effect at the resulting heterojunction interface is weak opposite to the case of a group-III nitride semiconductor heterojunction. SiC materials have similar chemical compositions (all composed of Si and C) even when having different crystal forms. This eliminates diffusive contamination of chemical components at a heterojunction between two SiC materials. Therefore, a SiC heterojunction has novel electrical, optical, and thermal properties, and is suitable for applications where high frequency, high temperature, high pressure, high power, low noise, and good resistance to corrosion are of concern, making it a subject that has high R&D value, promising application prospect, and high market potential.
About SiC heterojunctions, the underlying principles of their growth and experimental preparation have been reported. Growth of a SiC heterojunction is mainly achieved using chemical vapor transportation such as molecular beam epitaxy (MBE), epitaxy under vacuum (SEV), physical vapor transportation (PVT), chemical vapor deposition (CVD), and vapor-liquid-solid growth (VLS). The research group led by XU Peng-Shou in University of Science and Technology of China made a 6H/3C/6H-SiCmulti-layer on the 6H—SiC (0001) face of a 1350K substrate using solid-source molecular beam epitaxy (SSMBE) [LIU Jin-Feng, LIU Zhong-Liang, XU Peng-Shou et. al., Journal of Chemical Physics, Vol. 24 (2008): 571-575.]. The known heterojunction was grown in three stages: (1) when the Si flow was slightly excessive, the growth was in a two-dimensional step flow mode, where the epitaxial film remained the same crystal form as the substrate; (2) when the Si flow was then lowered, the growth turned to three-dimensional island growth; and (3) when the Si flow was restored to the initial, slightly excessive supply, the growth mode returned to two-dimensional step flow growth. The research group led by ZHANG Yu-Ming in Xidian University formed a 3C/4H—SiC heterojunction on a 1770 K temperature on-axis 4H—SiC (0001) Si-face substrate through formation of a stepwise hetero-epitaxial 3C—SiC film using hot-wall chemical vapor deposition (HWCVD) and mixed reaction gas (SiH4+C3H8+H2) [B. Xin, R. X. Jia, Y M. Zhang, et al., Applied Surface Science, Vol. 357 (2015): 985-993.]. German researchers, A. Fissel, et al., made a (4,6) h/3C/(4,6) h-SiCmulti-layer on a (4, 6) h-SiC substrate using SSMBE[A. Fissel, Physics Reports, Vol. 379 (2003): 149-255.], and grew a 3C—SiC film on a 1430 K on-axis substrate (4, 6) h-SiC (0001) by alternating C and Si sources during growth with a well-controlled twin boundary of the (4, 6) h/3C—SiC interface and a 3C—SiC layer having improved quality. Russian researchers, A. A. Lebedev, et al., developed a 3C/6H—SiC mutated heterojunction using SEV [A. A. Lebedev, et al., Journal of Crystal Growth, Vol. 396 (2014): 100-103.]. To grow 3C—SiC on the Si face of a substrate 6H—SiC (0001) required a temperature of 2270 K and the growth rate above 0.7 μm/min; and to grow 3C—SiC on the C (0001−) face of a 6H—SiC substrate required a temperature of 2120-2170 K, and the growth rate of 0.4˜0.5 μm/min. The peaks 2.9 eV and 2.3 eV in the electroluminescence spectrum corresponded to the bandgaps of 6H—SiC and 3C—SiC, respectively. French researchers, J. Lorenzzi, et al., used a water-based cold-wall CVD system and mixed gas of different formulas to make 3C/6H—SiC heterojunctions on on-axis and 2-degree-off-axis 6H—SiC (0001) Si-face substrates and investigated into VLS for 3C—SiC epitaxial growth [J. Lorenzzi, et al., Diamond & Related Materials, Vol. 20 (2011): 808-813.].
More studies have been made on SiC heterojunctions for their novel electrical, optical, and thermal properties. XIE Xi-De, et. al. of Fudan University, Chian, used the LMTO-ASA ab initio energy band method to identify the electronic structure and the band structure of superlattices at (3C—SiC)3n/(2H—SiC)2n (n=1, 2, 3) heterojunctions [X. D. Xie, et al., Physical Review B, Vol. 54 (1996): 8789-8793.], and the results indicated that a 3C/2H—SiC heterojunction had a type-II energy band, a conduction band offset ΔEc=1.48 eV, and valence band offset ΔEv=0.13 eV, with the bandgap decreased rapidly with increase of the overall thickness, which was believed to be related to the internal electric field caused by 2H—SiC spontaneous polarization, yet the electric field had little impact on band offsets ΔEc and ΔEv. Russian scientists, S. Yu. Davydov, et al. measured how the spontaneous polarization effect impacted the energy level of a (4, 6) h/3C/(4, 6) h-SiC heterojunction quantum well [S. Yu. Davydov, et al., Physics of the Solid State, Vol. 53 (2011): 872-877.; S. Yu. Davydov, et al., Semiconductors, Vol. 53 (2019): 699-702.]. Particularly, they solved Poisson Equation and Schrödinger Equation in a self-consistent manner by setting boundary conditions, so as to get an energy level expression for quantum wells at a SiC heterojunction. Simulative calculation demonstrated that spontaneous polarization narrowed and deepened the quantum well at the left interface of a (4, 6) h/3C/(4, 6) h-SiC heterojunction, and widened and shallowed the quantum well at the right interface. Electrons moved from the quantum wells in the 3C—SiC region directly to the valence band in the (4, 6) h-SiC region. When the 3C—SiC was very thin, electrons moved from the left conduction band quantum well indirectly to the valence band at the right interface. US scientists, M. V. S. Chandrashekhar, et. al made a 4H(0001−)C face/3C—SiC heterojunction using cold-wall CVD [M. V. S. Chandrashekhar, et al., Applied Physics Letters, Vol. 91 (2007): 033503-1-3.]. In the interface quantum wells of this heterojunction, the 3C—SiC side had two-dimensional electron gas (2DEG), with its mobility up to 314 cm2·V−1·s−1 and surface density up to 3×1013 cm−2. M. V. S. Chandrashekhar further prepared a 4H (0001) Si face/3C—SiC heterojunction [M. V. S. Chandrashekhar, et al., Applied Physics Letters, Vol. 90 (2007): 173509-1-4.], wherein 4H—SiC spontaneous polarization induced positive charges at the 3C—SiC side to form interface two-dimensional hole gas (2DHG), with a surface density up to 9.7×1012 cm−2. This is because spontaneous polarization induced a large amount of 2DHG. US scientists S. Bai, et. al. prepared 4H/3C/4H—SiC single quantum well at the temperature of 1820 K using hot-wall CVD [S. Bai, et al., Applied Physics Letters, Vol. 83 (2003): 3171-3173.]. According to a low-temperature PL spectrum at 2K, the light-emitting energy of the quantum well was 0.2 eV lower than the bandgap of the 3C—SiC body material, attributable to light-emitting redshift at quantum wells caused by the quantum-confined Stark effect resulted from the electric field induced by 4H—SiC spontaneous polarization. Accordingly, the intensity of 4H—SiC spontaneous polarization was calculated. US scientists Jie Lu, et. al formed a 6H(0001−)C face/3C—SiC heterojunction by depositing 3C—SiC on the C face of a substrate 6H—SiC (0001) using a cold-wall CVD system [J. Lu, et al., Applied Physics Letters, Vol. 94 (2009): 162115-1-3.]. Their analysis suggested that, between the 6H—SiC (0001) face and 3C—SiC (111), lattice mismatch was below 0.1%, and thermal mismatch was less than 0.1%. The measurements of magnetotransport in the 0˜10 T magnetic field and in the temperature range of 1.5˜100 K indicated that the heterojunction interface had 2DEG, with its mobility of 2000 cm2·V−1·s−1, and its surface density of (2.7±0.2)×1012 cm−2. When the magnetic field remained unchanged, the longitudinal magnetoresistance Rxx decreased as the temperature increased. When the temperature was below 30 K, Rxx decreased first and then increased as the magnetic field increased. When the temperature was high than 30K, Rxx increased with increase of the magnetic field.
To date, some SiC heterojunction devices and performance thereof have been reported. For example, R. A. Minamisawa et. al. prepared a 3C/4H—SiC heterojunction Schottky barrier diode (SBD) using an HWCVD method [R. A. Minamisawa, et al., Applied Physics Letters, Vol. 108 (2016): 143502-1-3.], with a forward voltage Von=1.65 V and a leakage current satisfying the field emission mechanism. The SBD had better thermal stability as compared to Si/SiC heterojunction SBDs prepared using CVD and MBE. The inventors of the present invention have designed a terahertz wave band SiC heterojunction impact ionization avalanche transit-time (IPATT) diode [W. S. Wei, et al., Superlattices and Microstructures, Vol. 152 (2021): 106844-1-12.]. Based on digital simulation, impact of the SiC heterojunction barrier and material properties on the performance of the device in terms of direct current and large signal before and after correction of quantum effects (i.e., tunneling, the Bohm potential) were analyzed, and different heterojunction IPATT diodes were compared in terms of power, efficiency, and noise.
Based on all the foregoing researches and studies, with the consideration of basic match of lattices in a and b directions at a 3C/4H(6H)—SiC heterojunction interface, with the piezoelectric polarization effect ignored, in such a heterojunction interface the only thing to be considered is interface 2DEG and 2DHG incurred by spontaneous polarization of hexagonal SiC, without the need of considering the interface piezoelectric polarization effect. Hence, there is a need for such a heterojunction device that minimizes interface 2DEG and 2DHG interference at the interface, so as to eliminate diffusive contamination across two sides of the heterojunction interface and reduce process complexity. Therefore, as compared to a device having a group-III nitride heterojunction that causes spontaneous, piezoelectric polarization, the disclosed SiC heterojunction device is simpler and more reliable.
Embodiments of the present invention solve the technical problems of the prior art by providing a silicon carbide (SiC) heterojunction normally-off high-electron-mobility transistor (HEMT) and a method for preparing the same. The method allows two sides of the SiC heterojunction interface have homogeneous elements during preparation, thereby eliminating diffusive contamination, simplifying manufacturing, and improving device performance.
To this end, in an embodiment of the present invention, a method for preparing a SiC heterojunction normally-off HEMT comprises the following steps:
Therein, the step S11 is achieved by:
Therein, the step S12 is achieved by:
Therein, the step S13 is achieved by:
Therein, the step S14 is achieved by:
Therein, the step S15 is achieved by:
Therein, the step S16 is achieved by:
Another embodiment of the present invention provides a method for preparing a SiC heterojunction normally-off HEMT, comprising the following steps:
Still another embodiment of the present invention provides a SiC heterojunction normally-off single-channel HEMT prepared using the method for preparing a silicon carbide heterojunction normally-off high-electron-mobility transistor as described previously.
Yet another embodiment of the present invention provides a SiC heterojunction normally-off double-channel HEMT prepared using the method for preparing a silicon carbide heterojunction normally-off high-electron-mobility transistor as described previously.
By implementing the embodiments of the present invention, the following beneficial effect can be achieved: As compared to traditional GaN-based heterojunction normally-off HEMTs, the disclosed SiC heterojunction single- and double-channel HEMTs are such prepared that two sides of the heterojunction interface have homogeneous elements (Si and C at the both sides), thereby eliminating diffusive contamination across the heterojunction interface, reducing process complexity, and improving device performance.
In order to better illustrate technical features of embodiments of the present invention or of the prior art, brief introduction to accompanying drawings used to describe embodiments of the present invention or of the prior art are provided below. Apparently, the accompanying drawings listed below merely refer to some but not all embodiments of the present invention. For those of ordinary skill in the art, more drawings can be derived from these drawings without paying creative efforts, and all these derived drawings will be part of the scope of the present invention.
For further illustrating the means and functions by which the present invention achieves the certain objectives, the following description, in conjunction with the accompanying drawings and preferred embodiments, is set forth as below to illustrate the implement, structure, features and effects of the subject matter of the present invention.
As shown in
At the step S11, an unintentionally doped n-type 4H—SiC chip is selected as a substrate.
Specifically, first, an unintentionally doped n-type 4H—SiC chip that is on-axis or is off-axis by a predetermined angle (e.g., 4°) is used as a substrate.
Secondary, at a first predetermined temperature (e.g., about 1850 K), hydrogen (H2) is introduced into the reaction chamber of a hot wall chemical vapor deposition (HWCVD) system at a low flow to etch the growth face of the 4H—SiC chip substrate, so as to remove dangling bonds, surface scratches, and smears.
The step S12 involves growing a 4H—SiC transition layer on an upper surface of the substrate through isomorphic epitaxial growth, and growing a C face on an upper surface of the 4H—SiC transition layer through epitaxial growth.
Specifically, the substrate temperature for the etching stage is held, and the flow of the introduced H2 is modulated. Also introduced are SiH4 and C3H8 as reaction source gases and PH3 as a doping gas, each at a proper flow. In this stage, the pressure inside the reaction chamber is held at 10 Pa. Then reflection high-energy electron diffraction (RHEED) is used to monitor the 4H—SiC growth face in situ for ensuring clearness of the resulting reconstructed pattern.
At this time, first, in the reaction chamber of the HWCVD system, under the first predetermined temperature (e.g., 1850 K) and the predetermined pressure (e.g., 10 Pa), with a first mixed gas formed by supplying silane (SiH4), propane (C3H8), hydrogen (H2), and phosphine (PH3) as a doping gas, the 4H—SiC transition layer, which is isomorphous to the substrate on the growth face of the substrate, is formed through isomorphic epitaxial growth, and then the C face is formed by performing two-dimensional epitaxial growth on the surface of the 4H—SiC transition layer (e.g., by reasonably modulating the flows of and the flow ratio between the SiH4 and C3H8 source gases, as well as the flow of the doping gas and the doping ratio PH3/SiH4, with the substrate temperature controlled precisely).
Secondary, the thickness of the 4H—SiC transition layer may be controlled by changing the growth rate, the growth time, and the RHEED pattern monitored in situ, and when the thickness of the C face 4H—SiC transition layer reaches the first predetermined thickness value (e.g., 2 um), supply of SiH4, C3H8, and PH3 to the first mixed gas is cut off and only H2 remains delivered to the chamber to etch and remove dangling bonds, surface scratches, and smears from the growth face of the 4H—SiC transition layer, thereby reducing defects and contributing to interface smoothness.
The step S13 involves growing an unintentionally doped 3C—SiC potential well layer on the C face of the 4H—SiC transition layer.
Specifically, first, in the reaction chamber of the HWCVD system, at a second predetermined temperature (e.g., 1750 K), with a second mixed gas formed by supplying SiH4, C3H8, and H2, three-dimensional island growth is performed on the C face of the 4H—SiC transition layer to form an unintentionally doped 3C—SiC potential well layer. That is, when the temperature decreases to about 1750K, a mixed reaction source gas (SiH4+C3H8+H2) of a reasonable formula is introduced, and the flow of the Si source gas (SiH4) is properly lowered while the flow of C3H8 is reasonably increased, with the pressure inside the reaction chamber (e.g., 10 Pa) held at the same level as that for the previous stage. Since the proportion of the Si source is lowered, the RHEED reconstructed pattern at the SiC growth face as monitored in situ transforms, making the growth mode at the surface of the 4H—SiC transition layer turn from two-dimensional step flow growth into three-dimensional island growth. At this time, the crystal form changes to 3C—SiC from 4H—SiC.
Secondary, the thickness of the 3C—SiC potential well layer may be controlled by changing the growth rate, the growth time, and the RHEED pattern monitored in situ, and when the thickness of the 3C—SiC potential well layer reaches the second predetermined thickness value (e.g., 25 nm), supply of SiH4 and C3H8 to the second mixed gas is cut off and only H2 remains delivered to the chamber to etch and remove dangling bonds, surface scratches, and smears from the growth face of the 3C—SiC potential well layer, thereby reducing defects and contributing to interface smoothness.
It is to be noted that the 3C—SiC potential well layer and the C face 4H—SiC transition layer form a SiC heterojunction interface, that excites the 2DEG.
The step S14 involves growing an n-type doped 4H—SiC barrier layer on an upper surface of the 3C—SiC potential well layer, and growing a Si face on an upper surface of the 4H—SiC barrier layer through epitaxial growth.
Specifically, in the reaction chamber of the HWCVD system, under the first predetermined temperature (e.g., 1850 K) and the predetermined pressure (e.g., 10 Pa), with the first mixed gas formed by supplying SiH4, C3H8, H2, and a proper proportion of PH3, the n-type doped 4H—SiC barrier layer is formed on the upper surface of the 3C—SiC potential well layer through two-dimensional step flow growth, and then the Si face is formed by performing epitaxial growth on the upper surface of the 4H—SiC barrier layer. To be specific, the parameters used in this stage are restored to the level used in the step S12, including the substrate temperature, the total amount and the formula of the mixed reaction source gas (SiH4+C3H8+PH3+H2), the pressure in the HWCVD reaction chamber, etc. At this time, the proportion of the Si source at the 4H—SiC growth face is larger than that used for 3C—SiC growth, and the RHEED pattern monitored in situ restores to the crystal form as seen in the growth of the 4H—SiC transition layer. The growth mode at the surface of the 4H—SiC barrier layer returns to two-dimensional step flow growth from three-dimensional island growth, and the film changes back to the 4H—SiC crystal form from the 3C—SiC crystal form.
Secondary, the thickness of the 4H—SiC barrier layer may be controlled by changing the growth rate, the growth time, and the RHEED pattern monitored in situ, and when the thickness of the Si face 4H—SiC barrier layer reaches the third predetermined thickness value (e.g., 25 nm), supply of SiH4, C3H8, and PH3 to the first mixed gas is cut off and only H2 remains delivered to the chamber to etch and remove dangling bonds, surface scratches, and smears from the growth face of the 4H—SiC barrier layer, thereby reducing defects and contributing to interface smoothness.
It is to be noted that for minimizing any adverse effect of lowering the temperature to growth of the layers, in the temperature-changing process during Step 12->Step 13->Step 14, supply of SiH4, C3H8, and PH3 is cut off and only H2 is used for etching the surfaces of the growth materials because the impact of etching is slower and weaker than that of temperature variation. This also prevents uneven among SiH4, C3H8, H2, and PH3 of the first mixed gas introduced into the HWCVD reaction chamber in the initial stage.
The step S15 is about growing an unintentionally doped 3C—SiC cap layer at the upper surface of the 4H—SiC barrier layer.
Specifically, the process repeats the process of the Step 13. To be specific, the parameters used in this stage are restored to the level used in the step S13, including the substrate temperature, the total amount and the formula of the mixed reaction source gas (SiH4+C3H8+H2), the pressure in the HWCVD reaction chamber, the process for preparing the 3C—SiC potential well layer, etc.
First, in the HWCVD reaction chamber held at the second predetermined temperature (e.g., 1750K), with the second mixed gas formed by supplying SiH4, C3H8, and H2, three-dimensional island epitaxial growth is performed on the surface of the 4H—SiC transition layer to form the unintentionally doped 3C—SiC cap layer.
Secondary, the thickness of the 3C—SiC cap layer may be controlled by changing the growth rate, the growth time, and the RHEED pattern monitored in situ, and when the thickness of the 3C—SiC cap layer reaches the fourth predetermined thickness value (e.g., 25 nm), supply of SiH4 and C3H8, to the second mixed gas is cut off and only H2 remains delivered to the chamber to etch and remove dangling bonds, surface scratches, and smears from the growth face of the 3C—SiC cap layer, thereby reducing defects and contributing to interface smoothness.
It is to be noted that 3C—SiC cap layer and the Si face 4H—SiC barrier layer form a SiC heterojunction interface, thereby exciting the 2DHG.
The step S16 involves producing electrodes and protective films, so as to obtain a 3C—SiC/4H—SiC heterojunction normally-off single-channel HEMT.
Specifically, first, inductively coupled plasma (ICP) etching is used to create, at each of two opposite sides of the multi-layer SiC heterojunction, a respective gate (G) trench for forming a longitudinally-conductive channel and a respective drain (D) trench for enabling ohmic contact between a drain and a 2DEG laterally-conductive channel. Therein, the multi-layer SiC heterojunction has a SiC heterojunction formed by the 4H—SiC transition layer and the 3C—SiC potential well layer that excite the 2DEG and a SiC heterojunction formed by the 4H—SiC barrier layer and the 3C—SiC cap layer that excite the 2DHG.
Second, ion implantation is used to implant phosphorus (P) ions with a concentration of Nm into the 3C—SiC cap layer below a source so as to form an N+-doped region for modulating a threshold voltage (Vth) of the HEMT and to implant P ions into the multi-layer SiC heterojunction left to the drain so as to form N+-doped regions for creating the ohmic contact between the 2DEG laterally-conductive channel and the drain.
As the third step, electron-beam evaporation is used to deposit alloy films in all of the N+-doped regions, respectively, so as to form sources (S) and drains (D) for the ohmic contact.
As the fourth step, electron-beam evaporation is used to apply an insulating gate medium into the G trench and to deposit a Schottky metal gate (G), wherein the insulating gate medium is one of SiO2, Al2O3, HfO2, and La2O3.
As the fifth step, the multi-layer SiC heterojunction is coated with a protective layer.
As the sixth step, a light shielding layer is coated onto the protective layer to prevent lateral light incidence and consequent impact on device performance.
Corresponding to the method for preparing a SiC heterojunction normally-off HEMT in Embodiment 1 of the present invention, Embodiment 1 of the present invention further provides a SiC heterojunction normally-off single-channel HEMT prepared using the method for preparing a SiC heterojunction normally-off HEMT in Embodiment 1 of the present invention. The details of the method have been described previously and are not repeated herein. The specific structure is as depicted in the cross-sectional view shown in
As shown in
It is to be noted that the step S21 has a detailed process identical to that of the step S11 in Embodiment 1 of the present invention; the step S22 has a detailed process identical to that of the step S12 in Embodiment 1 of the present invention; the step S23 and the step S25 have detailed processes identical to that of the step S13 in Embodiment 1 of the present invention; the step S24 has a detailed process similar to that of the step S12 in Embodiment 1 of the present invention except that the 4H—SiC first barrier layer is thinner than the 4H—SiC transition layer; the step S26 has a detailed process identical to that of the step S14 in Embodiment 1 of the present invention; the step S27 has a detailed process identical to that of the step S15 in Embodiment 1 of the present invention; and the step S28 has a detailed process identical to that of the step S16 in Embodiment 1 of the present invention. The details can be seen in the method for preparing a SiC heterojunction normally-off single-channel HEMT in Embodiment 1 of the present invention and repeated description is omitted herein.
Corresponding to the method for preparing a SiC heterojunction normally-off double-channel HEMT in Embodiment 2 of the present invention, Embodiment 2 of the present invention further provides a SiC heterojunction normally-off double-channel HEMT prepared using the method for preparing a SiC heterojunction normally-off double-channel HEMT in Embodiment 2 of the present invention. The details of the method have been described previously and are not repeated herein. The specific structure is as depicted in the cross-sectional view shown in
The parameters used for the SiC heterojunction normally-off double-channel HEMT of Embodiment 2 are shown in Table 1 below:
The 3C—SiC/4H—SiC heterojunction normally-off single, double-channel HEMT of the embodiment of the present invention will be further described for explaining its structure and working principles.
The present invention uses the spontaneous polarization effect of 4H—SiC to create two different SiC heterojunctions, namely 3C—SiC/4H—SiC (Si face) and 3C—SiC/4H—SiC (C face), as shown in
In
Additionally, the 2DHG at the 3C—SiC/4H—SiC (Si face) heterojunction interface can suppress the drain-induced barrier lowering effect caused by increase of the drain voltage. In a traditional HEMT, as the drain voltage increase, the barrier at the source decreases, so the number of electrons injected into the channel from the source increases significantly and the drain current increases consequently, leading to early breakdown of the HEMT. By contrast, in the disclosed HEMT, the 2DHG increases the conduction band barrier of the heterojunction below the source and prevents electrons from entering the channel from the source, thereby effectively suppressing the drain-induced barrier lowering effect and increasing the breakdown voltage of the device. Moreover, in the disclosed HEMT, the gate thickness has merely small impact on the drain-induced barrier lowering effect, and this allows the disclosed HEMT to be made compact in its lateral dimension.
Besides, the source acts as a floating field plate, which helps reduce the electric field peak at the edge of the gate, and further induce a new electric field peak at the right end of the source. Therefore, fixed positively and negatively polarized charges at 3C/4H—SiC (C face) and 3C/4H—SiC (Si face) interface and the source jointly enhance the lateral electric field of the disclosed HEMT, thereby increasing the breakdown voltage of the disclosed HEMT. Also, an N+-type heavily-doped region is introduced below the source to lower the conduction band barrier at the heterojunction where the 2DHG is located, so as to modulate the 2DHG concentration and lower the threshold voltage (Vth) of the disclosed HEMT. The higher the doing concentration (Nm) in the N+-type region is, the lower the concentration of the 2DHG below the source is, and the smaller Vth the device has.
By changing the doping concentration Nm in the heavily-doped region below the source, changing the gate oxide thickness, selecting different oxide materials, and changing the gate voltage, the energy-band structures of the oxide/semiconductor heterojunction of the disclosed single and double-channel HEMTs can be varied, and some related simulations are shown in
According to
With only the thickness of the gate oxide changed, the resulting conduction band and valence band are shown in
When different oxide insulating materials are used, the conduction band and the valence band vary as shown in
The electron-hole distributions in the 3C/4H—SiC heterojunction normally-off single- and double-channel HEMTs under different conditions are shown in
Fixed positively and negatively polarized charges at the 3C—SiC/4H—SiC (C face) heterojunction and the 3C—SiC/4H—SiC (Si face) heterojunction interface affect the SiC heterojunction normally-off single-channel HEMT in terms of potential distribution in a way shown in
Variation of the thickness (tc) of the 3C—SiC cap layer affects the SiC heterojunction normally-off single-channel HEMT in terms of performance in the way shown in
Variation of the thickness (tw) of the 3C—SiC potential well layer affects the SiC heterojunction normally-off single-channel HEMT in terms of performance in the way shown in
Variation of the thickness (tb) of the 4H—SiC barrier layer affects the SiC heterojunction normally-off single-channel HEMT in terms of performance in a way shown in
Variation of the P-type doping concentration (Pb) in the barrier layer 4H—SiC affects the SiC heterojunction normally-off single-channel HEMT in terms of performance in a way as shown in
The gate thickness Lg and the height tg affect the breakdown voltage (VB) and the specific on resistance (Ron, sp) of the SiC heterojunction normally-off double-channel HEMT in a way shown in
The characteristics of the disclosed single- and double-channel HEMTs in terms of transfer and output are shown in
The disclosed HEMT is small in specific on resistance (Ron, sp) and high in breakdown voltage (VB). In the disclosed HEMT, since the source and the drain are at the same side with respect to the gate, the lateral size of the device can be reduced effectively. Meanwhile, the disclosed HEMT uses 3C—SiC to form the potential well layer, wherein the 2DEG is more mobile than 4H—SiC. Particularly, the disclosed SiC heterojunction double-channel HEMT has a Ron, sp smaller than those reported in literature [Zhou Q, et al., IEEE Trans Electron Devices, Vol. 60 (2013): 1075-1081; Xiong J Y, et al., Science China Information Sciences, Vol. 59 (2016): 042410; Yang C, et al., Superlattice & Microstructures, Vol. 92 (2016): 92-99; Yang C, et al., Science China Information Sciences, Vol. 61 (2018): 062402]. On the other hand, it is right because the disclosed HEMT uses 3C—SiC and 4H—SiC having bandgaps much larger than that of Si, it has very high voltage endurance. For a power device at a given voltage level, the smaller Ron, sp of the device is, the greater the power figure of merit (FOM) value is. The disclosed single, double-channel HEMTs have FOM values of 2.58 MW/mm2 and 4.36 MW/mm2, respectively, representing good balance between VB and Ron, sp.
To sum up, the disclosed SiC heterojunction HEMT is a normally-off device with a relatively high breakdown voltage and a relatively low threshold voltage (Vth). Its specific on resistance is very small and reliability is high. In addition, the device can be made compact in the lateral dimension making it contributive to enhanced integration and design freedom of power ICs. Different crystals in the SiC heterojunction are basically alike in terms of lattice constant and thermal conductivity, and the piezoelectric polarization effect at the heterojunction interface is ignorable, so the modulation parameters can be simplified. Meanwhile, since the crystals forming SiC have similar chemical properties, diffusive contamination among chemical components during preparation of the device can be eliminated, thereby ensuring stable performance.
By implementing the embodiments of the present invention, the following beneficial effect can be achieved:
As compared to traditional GaN-based heterojunction normally-off HEMTs, the disclosed SiC heterojunction single- and double-channel HEMTs are such prepared that two sides of the heterojunction interface have homogeneous elements (Si and C at the both sides), thereby eliminating diffusive contamination across the heterojunction interface, reducing process complexity, and improving device performance.
The present invention has been described with reference to the preferred embodiments and it is understood that the embodiments are not intended to limit the scope of the present invention. Moreover, as the contents disclosed herein should be readily understood and can be implemented by a person skilled in the art, all equivalent changes or modifications which do not depart from the concept of the present invention should be encompassed by the appended claims.
Number | Date | Country | Kind |
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202211080038.5 | Sep 2022 | CN | national |
Filing Document | Filing Date | Country | Kind |
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PCT/CN2022/119679 | 9/19/2022 | WO |