The present invention relates to a method of manufacturing a hybrid substrate.
Bulk silicon (Si) complementary metal-oxide-semiconductor (CMOS) devices scaling, which is the main enabler for the semiconductor industry to maintain device performance, lower power consumption of CMOS devices, and reduce cost per transistor, is now reaching the fundamental bottleneck. Further shrinkage of CMOS devices not only causes the CMOS devices to be unreliable performance-wise, but also increases costs to produce the CMOS devices. To address the problem, amongst electronic materials being considered as suitable candidates for adoption in the post-silicon era, III-V compounds (e.g. gallium arsenide (GaAs)) appear to be the most promising due to their characteristics of having considerably higher carrier mobility (notably electrons), which are suited for implementing high-speed special-purpose devices. Also, GaAs can be used as a light source to be integrated with optical amplifiers and detectors onto Si-based chips or waveguides (“hybrid devices”) to enhance performance and design flexibility for photonic interconnects. Such hybrid devices compensate for the poor ability of Si to act as a light source, thus opening-up possible new circuit capabilities and applications.
To realise the hybrid devices, a first step is to be able to obtain high quality GaAs layers arranged on a Si substrate, creating an alternative substrate. Alternative GaAs-on-Si substrates have huge market potential as replacement for expensive and much smaller substrates that are currently used to produce conventional GaAs-based devices (e.g. microwave devices, solar cells, or photodetectors). Moreover, alternative GaAs-on-Si substrates also enable development of monolithic integration technology for GaAs and Si integrated circuits (ICs).
GaAs epitaxial film can be grown directly on a Si substrate using metal-organic chemical vapour deposition (MOCVD), or molecular beam epitaxy (MBE). However, in either case, crystal imperfections tend to be created due to the large lattice mismatch (i.e. about 4%), and due to difference in thermal expansion coefficients (i.e. 6.63×10−6 K−1 for GaAs, and 2.3×10−6 K−1 for Si) between GaAs and Si. Hence, direct growth of a GaAs epilayer on a Si substrate usually results in fairly high dislocation densities of around 109-1010/cm2. Through very careful selection of suitable temperatures used in the two-step GaAs growth and thermal cycling (i.e. 950° C. to 300° C., for 4 cycles), the best reported dislocation values are nonetheless greater than 1×107/cm2, which is still not ideal.
Researchers have also been inserting various kinds of buffer layers between the Si substrate and the GaAs epilayer. The most explored buffer layer is using germanium (Ge). Basically, a thick Si1-xGex (about 10 μm) is graded from x=0 to x=1 on a Si substrate, followed by GaAs epilayer growth. Through this technique, the reported treading dislocation density (TDD) is about 7×106/cm2. Another method is to use gallium phosphide (GaP), which has a lattice constant differing from Si by 0.37%, followed by depositing variable-composition buffer layers (e.g. GaAsP or InGaP), until the lattice is substantially matched with GaAs. In this case, the TDD achieved is about 1×107/cm2. A further method is via selective area growth using a patterned SiO2 mask. For this method, the reported TDD is about 5×106/cm2.
One object of the present invention is therefore to address at least one of the problems of the prior art and/or to provide a choice that is useful in the art.
According to a 1st aspect, there is provided a method of manufacturing a hybrid substrate, comprising: (i) bonding a first semiconductor substrate to a first combined substrate via at least one layer of dielectric material to form a second combined substrate, the first combined substrate includes a layer of III-V compound semiconductor and a second semiconductor substrate, the layer of III-V compound semiconductor arranged intermediate the layer of dielectric material and second semiconductor substrate; (ii) removing the second semiconductor substrate from the second combined substrate to expose at least a portion of the layer of III-V compound semiconductor to obtain a third combined substrate; and (iii) annealing the third combined substrate at a temperature about 250° C. to 1000° C. to reduce threading dislocation density of the layer of III-V compound semiconductor to obtain the hybrid substrate.
For example, if GaAs is adopted as the layer of III-V compound semiconductor, the method advantageously allows the GaAs crystal to undergo re-crystallization at a sufficient high temperature, since the GaAs layer is no longer restricted by the donor substrate (i.e. the second semiconductor substrate), after the donor substrate has been removed.
Preferably, subsequent to step (i) and prior to step (ii), the method may further comprise inverting the second combined substrate.
Preferably, step (ii) may include using a combination of mechanical grinding and wet-etching the second combined substrate in a solution of tetramethylammonium hydroxide to remove the second semiconductor substrate.
Preferably, the annealing may be performed using a gas selected from the group consisting of oxygen, hydrogen, nitrogen, forming gas, helium, and argon.
Preferably, the layer of dielectric material may be formed on the first combined substrate, and arranged adjacent to the layer of III-V compound semiconductor.
Preferably, the layer of dielectric material may be formed using plasma-enhanced chemical vapour deposition or atomic layer deposition.
Preferably, the dielectric material may be selected from the group consisting of aluminium oxide, aluminium nitride, silicon dioxide, synthetic diamond, silicon nitride and boron nitride.
Preferably, the first and second semiconductor substrates may respectively be formed from a silicon-based material.
Preferably, the second semiconductor substrate may be a silicon substrate with 6° off-cut toward [111] direction.
Preferably, prior to the bonding, the method may further comprise: performing plasma cleaning on the first combined substrate and first semiconductor substrate; washing the cleaned first combined substrate and first semiconductor substrate with a deionized fluid; and drying the washed first combined substrate and first semiconductor substrate.
Preferably, the deionized fluid may be deionized water.
Preferably, drying the washed first combined substrate and first semiconductor substrate may include using spin-drying.
Preferably, step (i) may further include annealing the second combined substrate to increase the bonding between the first semiconductor substrate and the layer of dielectric material.
Preferably, the annealing may be performed using nitrogen at a temperature of about 300° C. and at atmosphere pressure.
Preferably, the plasma cleaning may be performed with oxygen plasma, hydrogen plasma, argon plasma, or nitrogen plasma.
Preferably, the method may further comprise depositing a layer of protective material on the first semiconductor substrate, subsequent to step (i) and prior to step (ii).
Preferably, the protective material may include ProTEK® B3-25, silicon dioxide or silicon nitride.
Preferably, step (ii) may further comprise: (iv) at least partially grinding the second semiconductor substrate; (v) arranging the second combined substrate to be in a first solution of tetramethylammonium hydroxide to remove the second semiconductor substrate; and (vi) performing etch-stopping on the exposed portion of the layer of III-V compound semiconductor.
Preferably, the first solution may be heated to a temperature of about 80° C. Preferably, the method may further comprise removing the protective material from the second semiconductor substrate using acetone or oxygen plasma configured with a power of about 800 W, subsequent to step (v).
Preferably, the at least one layer of dielectric material may include a plurality of layers of different dielectric materials.
According to a 2nd aspect, there is provided a method of manufacturing a hybrid substrate, comprising: (i) bonding a first semiconductor substrate to a first combined substrate via at least one layer of dielectric material to form a second combined substrate, the first combined substrate includes a germanium layer, a layer of III-V compound semiconductor and a second semiconductor substrate, the germanium layer arranged intermediate the second semiconductor substrate and layer of III-V compound semiconductor, the layer of III-V compound semiconductor arranged intermediate the layer of dielectric material and germanium layer; (ii) removing the second semiconductor substrate and germanium layer from the second combined substrate to expose at least a portion of the layer of III-V compound semiconductor to obtain a third combined substrate; and (iii) annealing the third combined substrate at a temperature about 250° C. to 1000° C. to reduce threading dislocation density of the layer of mixed compound materials to obtain the hybrid substrate.
Preferably, step (ii) may include: (iv) using a combination of mechanical grinding and wet-etching the second combined substrate in a first solution of tetramethylammonium hydroxide to remove the second semiconductor substrate.
Preferably, subsequent to step (iv), the method may further comprise using a second solution which includes 10% of hydrogen peroxide to remove the germanium layer.
Preferably, the layer of dielectric material may be formed on the first combined substrate.
Preferably, the at least one layer of dielectric material may include a plurality of layers of different dielectric materials.
It should be apparent that features relating to one aspect of the invention may also be applicable to the other aspects of the invention.
These and other aspects of the invention will be apparent from and elucidated with reference to the embodiments described hereinafter.
Embodiments of the invention are disclosed hereinafter with reference to the accompanying drawings, in which:
It is to be appreciated that both the first and second semiconductor substrates 102, 110 are respectively formed from a silicon-based material. In this case, both the first and second semiconductor substrates 102, 110 are formed from silicon (Si), and moreover, the second semiconductor substrate 110 is an epi-ready <100> orientated Si wafer substrate with 6° off-cut towards the nearest [111] direction. Also, the first and second semiconductor substrates 102, 110 may respectively be termed a Si handler substrate, and a Si donor substrate. Furthermore, a two-step GaAs growth was used to grow the GaAs epilayer (i.e. the layer of III-V compound semiconductor 108) directly on a Si donor wafer (i.e. the second semiconductor substrate 110) to obtain the first combined substrate 104.
Separately, it is to be appreciated that the layer of dielectric material 106 (e.g. 500 nm thick) serves as a capping layer for the layer of III-V compound semiconductor 108 (with regard to the first combined substrate 104), and also provides a bonding interface at step 152 (described below). The dielectric material is selected from the group consisting of aluminium oxide (Al2O3), aluminium nitride (AlN), silicon dioxide (SiO2), synthetic diamond, silicon nitride (Si3N4) and boron nitride (BN), but other suitable dielectric materials are usable too. The layer of dielectric material 106 is formed using, for example, plasma-enhanced chemical vapour deposition (PECVD) or atomic layer deposition to deposit the dielectric material onto the layer of III-V compound semiconductor 108. It is to be appreciated that in variant embodiments, the layer of dielectric material 106 can instead be formed on the first semiconductor substrate 102, rather than on the first combined substrate 104. Yet alternatively, respective layers of (same/different) dielectric material(s) may be formed on the first semiconductor substrate 102 and first combined substrate 104, and then the respective layers of dielectric material(s) are bonded together at step 152 (in the process of bonding the first semiconductor substrate 102 to the first combined substrate 104). Moreover, it is also possible that a plurality of layers of different dielectric materials (and combinations thereof) may be formed on the first combined substrate 104, if desired, instead of just a single layer 106.
At step 152 (i.e.
It is also to be highlighted that optionally, subsequent to step 150 and prior to step 152, plasma cleaning (e.g. using oxygen plasma, hydrogen plasma, argon plasma, or nitrogen plasma) may be performed on the first semiconductor substrate 102, and first combined substrate 104 for about 15 seconds each, followed by washing the cleaned first semiconductor substrate 102, and first combined substrate 104 with a deionized fluid (e.g. deionized water), and finally drying (e.g. spin-drying) the washed first semiconductor substrate 102, and first combined substrate 104. These additional steps are taken to better prepare the first semiconductor substrate 102, and first combined substrate 104 for the bonding at step 152.
Next at step 154 (i.e.
At further step 156 (i.e.
It is to be appreciated that subsequent to step 154 and prior to step 156, a layer of protective material (not shown) (e.g. ProTEK® B3-25, silicon dioxide (SiO2), silicon nitride (SiN), or combinations thereof) may optionally be deposited on the first semiconductor substrate 102. Specifically, the protective material is spin coated on a first surface of the first semiconductor substrate 102, the first surface opposing a second surface (of the first semiconductor substrate 102) on which the dielectric material 106 is arranged adjacent, to act as a protection layer during the process of removing the second semiconductor substrate 110.
After the second semiconductor substrate 110 has been completely removed with no existence of bubbles observed, the coating of protective material is removed from the first semiconductor substrate 102 using oxygen plasma configured with an operating power of about 800 W. Alternatively, the coating of protective material may be removed using acetone.
At step 158 (i.e.
The remaining configurations/embodiments will be described hereinafter. For the sake of brevity, description of like elements, functionalities and operations that are common between the different configurations/embodiments are not repeated; reference will instead be made to similar parts of the relevant configuration(s)/embodiment(s).
According to a second embodiment,
The layer of dielectric material 806 (e.g. 500 nm thick) serves as a capping layer for the layer of III-V compound semiconductor 808 (with regard to the first combined substrate 804), and then provide a bonding interface at step 852. The layer of dielectric material 806 can be formed using PECVD, or atomic layer deposition to deposit the dielectric material onto the layer of III-V compound semiconductor 808. It is to be appreciated that in variant embodiments, the layer of dielectric material 806 may instead be formed on the first semiconductor substrate 802, rather than on the first combined substrate 804. Yet alternatively, respective layers of (same/different) dielectric material(s) may be formed on the first semiconductor substrate 802 and first combined substrate 804, and then the respective layers of dielectric material(s) are bonded together at step 852 (in the process of bonding the first semiconductor substrate 802 to the first combined substrate 804). Also, it is possible that a plurality of layers of different dielectric materials (and combinations thereof) may be formed on the first combined substrate 804, if desired.
At step 852 (i.e.
It is also to be highlighted that optionally, subsequent to step 850 and prior to step 852, plasma cleaning (e.g. using oxygen plasma, hydrogen plasma, argon plasma, or nitrogen plasma) may be performed on the first semiconductor substrate 802, and first combined substrate 804 for about 15 seconds each, followed by washing the cleaned first semiconductor substrate 802, and first combined substrate 804 with a deionized fluid (e.g. deionized water), and finally drying (e.g. spin-drying) the washed first semiconductor substrate 802, and first combined substrate 804. These additional steps are taken to prepare the first semiconductor substrate 802, and first combined substrate 804 for the bonding at step 852.
Next at step 854 (i.e.
It is to be appreciated that subsequent to step 854 and prior to step 856, a layer of protective material (not shown) (e.g. ProTEK® B3-25, SiO2, SiN, or combinations thereof) may optionally be deposited on the first semiconductor substrate 802. Specifically, the protective material is spin coated on a first surface of the first semiconductor substrate 802, the first surface opposing a second surface (of the first semiconductor substrate 802) on which the dielectric material 806 is arranged adjacent, to act as a protection layer during the process of removing the second semiconductor substrate 812.
After the second semiconductor substrate 812 has been completely removed with no existence of bubbles observed, the coating of protective material is then removed from the first semiconductor substrate 802 using oxygen plasma configured with an operating power of about 800 W. Alternatively, the coating of protective material may also be removed using acetone. Then, at subsequent step 858 (i.e.
At step 860 (i.e.
With reference to the variant method 800,
In summary, the proposed method 100, 800 discloses a way to improve the crystal quality of GaAs (or the like) through thermal cycling, or annealing. It is envisaged that similar mechanism is expected and so the method 100, 800 should be applicable also to improve the crystal quality of other III-As/P-based materials system, e.g. InGaAs, InP, InGaP, InGaAsP and etc. To briefly reiterate, the proposed method 100, 800 broadly requires bonding a GaAs/Si or a GaAs/Ge/Si donor substrate (i.e. if the layer of III-V compound semiconductor 108, 808 is GaAs in one case) to a Si handler substrate via at least one layer of dielectric material 106, 806, and then followed by releasing the Si donor substrate to form a GaAs-OI substrate (i.e. the hybrid substrate 180, 880). More specifically, the method 100, 800 allows the GaAs crystal to undergo re-crystallization at a sufficient high temperature, since the GaAs layer is not restricted by the donor substrate (which is Si in this case) anymore, after removal of the donor substrate.
It is to be appreciated the potential commercial applications for the hybrid substrate 180, 880 (obtained by means of the proposed method 100, 800) include usage as a base substrate for subsequent III-V materials growth (e.g. InGaAs, InP and etc), usage in silicon photonics (e.g. GaAs lasers and detectors), and usage as a higher mobility channel for advanced CMOS devices.
While the invention has been illustrated and described in detail in the drawings and foregoing description, such illustration and description are to be considered illustrative or exemplary, and not restrictive; the invention is not limited to the disclosed embodiments. Other variations to the disclosed embodiments can be understood and effected by those skilled in the art in practising the claimed invention. For avoidance of doubt, the relative thicknesses of the different layers shown in
Further, at step 150, the first combined substrate 104 may instead be provided above the first semiconductor substrate 102, and the vertical orientation of the first combined substrate 104 is such that the layers are now arranged as (from top to bottom sequentially): the second semiconductor substrate 110, the layer of III-V compound semiconductor 108, and the layer of dielectric material 106. With this, step 154 can be skipped, and the method progresses directly to step 156. To clarify, this is a matter of simply orientating the first combined substrate 104 and the first semiconductor substrate 102, and does not in any way affect performance of the disclosed method 100. The above said also applies similarly, mutatis mutandis, to step 850 of the second embodiment.
Filing Document | Filing Date | Country | Kind |
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PCT/SG2016/050557 | 11/10/2016 | WO | 00 |
Number | Date | Country | |
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62285933 | Nov 2015 | US |