COMBINED EPITAXIAL GROWTH SYSTEM HAVING MULTIPLE REACTION CHAMBERS, OPERATION METHOD, DEVICE, AND MANUFACTURED CHIP AND APPLICATION THEREOF
20230387349 · 2023-11-30
Inventors
Cpc classification
International classification
H01L25/075
ELECTRICITY
H01L33/00
ELECTRICITY
Abstract
The present disclosure provides a combined epitaxial growth system having multiple reaction chambers, an operation method, a device, and a manufactured chip and an application thereof. With a special metal-organic chemical vapor deposition (MOCVD) machine, a group III-V compound epi-wafer and a group II-VI compound epi-wafer are sequentially grown on a substrate. A time interval a at which multiple group III-V compound reaction chambers are sequentially started is the same as growth time y of the group II-VI compound epi-wafer. With the multi-chamber and stepwise manner, not only are a group III-V compound and a group II-VI compound deposited in the reaction chambers more effectively, but the time division multiplexing (TDM), effective integration of the stepwise process, and capacity matching are also implemented. The present disclosure further provides a combined epitaxial growth device having multiple reaction chambers, including a first growth device, a feeding device and a second growth device.
Claims
1. A combined epitaxial growth system having multiple reaction chambers, comprising: a first growth device, wherein the first growth device is an metal-organic chemical vapor deposition (MOCVD) machine for preparing a group III-V compound, multiple group III-V compound reaction chambers are formed in the MOCVD machine, and the group III-V compound reaction chambers each are configured to prepare a group III-V compound epi-wafer; a second growth device, wherein the second growth device is an MOCVD machine for preparing a group II-VI compound, a group II-VI compound reaction chamber is formed in the MOCVD machine, and the group II-VI compound reaction chamber is configured to prepare a group II-VI compound epi-wafer; and a feeding device, wherein the multiple group III-V compound reaction chambers are sequentially started in terms of a same time interval; and assuming that the time interval is a, a>0, the group III-V compound epi-wafer has growth time of x, x>0, and the group II-VI compound epi-wafer has growth time of y, y>0, there is a need to satisfy a=y.
2. The combined epitaxial growth system according to claim 1, wherein the second growth device is replaced with an MOCVD machine for preparing a group III-VI compound, and a group III-VI compound reaction chamber is formed in the MOCVD machine and configured to prepare a group III-VI compound epi-wafer.
3. The combined epitaxial growth system according to claim 1, wherein there is one group II-VI compound reaction chamber.
4. An operation method of the combined epitaxial growth system having multiple reaction chambers according to claim 1, wherein the operation method assumes that there are n group III-V compound reaction chambers, n being an integer greater than 0, and comprises the following steps: 1) preparing group III-VI compound epi-wafers: taking substrates, placing the substrates into the group III-V compound reaction chambers respectively, assuming that i has an initial value of 1, a value of the i being in a range of [1, n], starting an ith group III-V compound reaction chamber, and starting the ith group III-V compound reaction chamber after a period of at least (i−1)y, thereby obtaining group III-V compound epi-wafers on surfaces of the substrates in all of the group III-V compound reaction chambers; 2) starting the feeding device, increasing the value of the i by 1, and transferring a group III-V compound epi-wafer in the ith group III-V compound reaction chamber to the group II-VI compound reaction chamber in the second growth device after a period of at least x+(i−1)y; 3) preparing a chip: starting the group II-VI compound reaction chamber, and obtaining, after a period of at least x+iy, a chip with a group II-VI compound epi-wafer covering a surface of the group III-V compound epi-wafer; 4) removing the chip from the group II-VI compound reaction chamber, and supplementing a substrate to the vacant group III-V compound reaction chamber; and 5) going back to step 2) if inn, and setting the value of the i as 1 and going back to step 2) if i=n; or ending a reaction if group III-VI compound epi-wafers generated in remaining group III-V compound reaction chambers are all transferred to the group II-VI compound reaction chamber sequentially to obtain the chip.
5. The operation method according to claim 4, wherein the second growth device is replaced with an MOCVD machine for preparing a group III-VI compound, and a group III-VI compound reaction chamber is formed in the MOCVD machine and configured to prepare a group III-VI compound epi-wafer.
6. The operation method according to claim 4, wherein there is one group II-VI compound reaction chamber.
7. The operation method according to claim 4, wherein the number n of the group III-V compound reaction chambers, the x and the y satisfy: n=x/y if a value of x/y is a positive integer; and n=x/y and the value of the n is obtained by rounding up if the value of x/y is not the positive integer.
8. The operation method according to claim 5, wherein the number n of the group III-V compound reaction chambers, the x and the y satisfy: n=x/y if a value of x/y is a positive integer; and n=x/y and the value of the n is obtained by rounding up if the value of x/y is not the positive integer.
9. The operation method according to claim 6, wherein the number n of the group III-V compound reaction chambers, the x and the y satisfy: n=x/y if a value of x/y is a positive integer; and n=x/y and the value of the n is obtained by rounding up if the value of x/y is not the positive integer.
10. The operation method according to claim 4, wherein a tray is provided in each of the group II-VI compound reaction chamber and the group III-V compound reaction chamber; the tray is preferably a graphite tray; and the operation method further comprises an annealing step with furnace annealing and a P-type annealing furnace between step 1) and step 3), a step of preheating the group II-VI compound reaction chamber before starting the group II-VI compound reaction chamber in step 3), a step of baking the tray between step 3) and step 4), and a step of suspending operation between step 4) and step 5) for a period which is greater than 0 and is preferably 1 h.
11. The operation method according to claim 5, wherein a tray is provided in each of the group II-VI compound reaction chamber and the group III-V compound reaction chamber; the tray is preferably a graphite tray; and the operation method further comprises an annealing step with furnace annealing and a P-type annealing furnace between step 1) and step 3), a step of preheating the group II-VI compound reaction chamber before starting the group II-VI compound reaction chamber in step 3), a step of baking the tray between step 3) and step 4), and a step of suspending operation between step 4) and step 5) for a period which is greater than 0 and is preferably 1 h.
12. The operation method according to claim 6, wherein a tray is provided in each of the group II-VI compound reaction chamber and the group III-V compound reaction chamber; the tray is preferably a graphite tray; and the operation method further comprises an annealing step with furnace annealing and a P-type annealing furnace between step 1) and step 3), a step of preheating the group II-VI compound reaction chamber before starting the group II-VI compound reaction chamber in step 3), a step of baking the tray between step 3) and step 4), and a step of suspending operation between step 4) and step 5) for a period which is greater than 0 and is preferably 1 h.
13. A combined epitaxial growth device having multiple reaction chambers, comprising: a first growth device, wherein the first growth device is a metal-organic chemical vapor deposition (MOCVD) machine for preparing a group III-V compound, and multiple group III-V compound reaction chambers are formed in the MOCVD machine and configured to prepare a group III-V compound epi-wafer respectively; a second growth device, wherein the second growth device is an MOCVD machine for preparing a group II-VI compound, and a group II-VI compound reaction chamber is formed in the MOCVD machine and configured to prepare a group II-VI compound epi-wafer; and a feeding device, wherein the feeding device is a feeding box, and an actuator arm is provided in the feeding device.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0047] In order to more clearly illustrate the technical solutions in the embodiments of the present disclosure, a brief introduction to the accompanying drawings required for the embodiments will be provided below. Apparently, the described embodiments are merely a part rather than all of the embodiments of the present disclosure. Those skilled in the art can obtain other solutions and drawings based on these drawings without creative efforts.
[0048]
[0049]
[0050]
[0051]
DETAILED DESCRIPTION OF THE EMBODIMENTS
[0052] The present disclosure will be described below in detail with reference to the embodiments, so as to facilitate understanding of those skilled in the art to the present disclosure. It is to be noted that the embodiments are merely used to further illustrate the present disclosure, rather than limit the protection scope of the present disclosure. Any unessential improvement and adjustment made to the present disclosure according to the contents of the present disclosure should be included in the protection scope of the present disclosure. Furthermore, any raw materials not described below in detail are all commercially available products. Any steps or extracting methods not described in detail are all steps or extracting methods known to those skilled in the art.
[0053]
[0054] Further, the present disclosure can further regulate the performance of the epitaxial material by introducing a doping element such as Si and Mg. For example, after Mg is doped, the p-GaN (P-type GaN) epitaxial material generated has a higher hole concentration. After Si is doped, the n-GaN (N-type GaN) epitaxial material generated has a higher electron concentration.
[0055]
[0056]
Embodiment 1
[0057] A first MOCVD machine for producing a GaN epi-wafer and a second MOCVD machine for producing a ZnO thin film are used. Assuming that the GaN epi-wafer has growth time of 6 h and the ZnO thin film has growth time of 2.5 h (=preheating time 0.5 h+actual growth time 2 h of the ZnO thin film), there are 6/2.5=2.4 GaN reaction chambers, namely three GaN reaction chambers, and one ZnO reaction chamber. All reaction chambers are connected in production, as shown in
[0058] The combined epitaxial growth in the embodiment is as follows: [0059] 1) The graphite tray 11 with the substrate 10 is placed into the sample inlet 4. An interface of the sample inlet 4 with the outside is closed, while an interface with the feeding box 8 is opened. The actuator arm 9 feeds the graphite tray 11 with the substrate 10 to the feeding box 8. The interface between the sample inlet 4 and the feeding box 8 is closed. Air in the feeding box 8 is extracted to create a vacuum environment. An interface between the first GaN reaction chamber 2A and the feeding box is opened. The actuator arm 9 feeds the graphite tray 11 with the substrate 10 to the first GaN reaction chamber 2A. The actuator arm 9 exits from the first GaN reaction chamber 2A. The first GaN reaction chamber 2A is sealed, and the vacuum environment is created. [0060] 2) The second graphite tray 11 with the substrate 10 is placed into the sample inlet 4. The interface of the sample inlet 4 with the outside is closed, while the interface with the feeding box 8 is opened. The actuator arm 9 feeds the graphite tray 11 with the substrate 10 to the feeding box 8. The interface between the sample inlet 4 and the feeding box 8 is closed. Air in the feeding box 8 is extracted to create the vacuum environment. An interface between the second GaN reaction chamber 2B and the feeding box is opened. The actuator arm 9 feeds the second graphite tray 11 with the substrate 10 to the second GaN reaction chamber 2B. The actuator arm 9 exits from the second GaN reaction chamber 2B. The second GaN reaction chamber 2B is sealed, and the vacuum environment is created. [0061] 3) The third graphite tray 11 with the substrate 10 is placed into the sample inlet 4. The interface of the sample inlet 4 with the outside is closed, while the interface with the feeding box 8 is opened. The actuator arm 9 feeds the graphite tray 11 with the substrate 10 to the feeding box 8. The interface between the sample inlet 4 and the feeding box 8 is closed. Air in the feeding box 8 is extracted to create the vacuum environment. An interface between the third GaN reaction chamber 2C and the feeding box is opened. The actuator arm 9 feeds the third graphite tray 11 with the substrate 10 to the third GaN reaction chamber 2C. The actuator arm 9 exits from the third GaN reaction chamber 2C. The third GaN reaction chamber 2C is sealed, and the vacuum environment is created. [0062] 4) A timing program is set. The GaN reaction chambers are started at a time interval of 2.5 h. The first GaN reaction chamber 2A is started, preheated and injected with the gas. The second reaction chamber 2B is started, preheated and injected with the gas after 2.5 h of preheating and gas injection of the first GaN reaction chamber 2A. The third reaction chamber 2C is started, preheated and injected with the gas after 5 h of preheating and gas injection of the first GaN reaction chamber 2A.
[0063] Specifically, upon completion of 6-h growth of the GaN epi-wafer in the first GaN reaction chamber 2A, the first GaN reaction chamber 2A is opened. The actuator arm 9 takes out the graphite tray 11 with the substrate 10 after the GaN epi-wafer is grown completely in the first GaN reaction chamber 2A. The first GaN reaction chamber 2A is sealed. The actuator arm 9 extracts the gas in the feeding box 8 to create the vacuum environment. The P-type annealing furnace 6 is opened. The actuator arm 9 feeds the graphite tray from the feeding box 8 to the P-type annealing furnace 6. The P-type annealing furnace 6 anneals the graphite tray 11, on which the GaN epi-wafer is grown completely, for 1 min (the reference time is 20 s to 3 min, and the annealing time can be adjusted according to the specific process). After the P-type annealing step on the graphite tray 11 on which the GaN epi-wafer is grown completely, the P-type annealing furnace 6 is opened, the actuator arm 9 takes out the previously fed graphite tray 11, and the P-type annealing furnace 6 is closed. Both the actuator arm 9 and the graphite tray 11 are located in the feeding box 8. The gas in the feeding box is extracted to create the vacuum environment. The interface between the ZnO reaction chamber 3 and the feeding box 8 is opened. The actuator arm 9 feeds the graphite tray 11 to the ZnO reaction chamber 3. The interface between the ZnO reaction chamber 3 and the feeding box 8 is closed. After 0.5 h upon completion of the growth on the graphite tray 11 with the substrate 10 in the first GaN reaction chamber 2A, the ZnO reaction chamber 3 starts to work, and the transparent ZnO electrode thin film is grown on the graphite tray 11 for 2 h (the reference time is 2-3 h and the growth time can be adjusted according to the specific process). Upon completion of the growth of the thin film, the interface between the ZnO reaction chamber 3 and the feeding box 8 is opened.
[0064] The actuator arm 9 takes out the graphite tray 11, the interface between the ZnO reaction chamber 3 and the feeding box 8 is closed, both the graphite tray 11 and the actuator arm 9 are located in the feeding box 8, and the gas in the feeding box 8 is extracted to create the vacuum environment. The sample outlet 5 is opened, the actuator arm 9 feeds the graphite tray to the sample outlet 5, the chip grown completely is taken out through the sample outlet 5 and fed to the outside, and the graphite tray 11 still remains on the actuator arm 9. After the finished chip is taken out, the actuator arm 9 brings the graphite tray 11 back to the feeding box 8. The graphite tray baking furnace 7 is opened, the actuator arm 9 feeds the graphite tray 11 to the graphite tray baking furnace 7, the actuator arm 9 returns to the feeding box 8, and the graphite tray baking furnace 7 is closed. The graphite tray baking furnace 7 is heated, until GaN and ZnO residues on the graphite tray 11 are vaporized. The graphite tray baking furnace 7 discharges vaporized gas, and the graphite tray 11 becomes clean again. The interface between the graphite tray baking furnace 7 and the feeding box 8 is opened, and the actuator arm 9 takes out the graphite tray 11. The graphite tray baking furnace 7 is closed, the sample inlet 4 is opened, and the actuator arm 9 feeds the graphite tray 11 to the sample inlet 7. The graphite tray 11 with the substrate 10 is replaced, the interface of the sample inlet 4 with the outside is closed, and the interface between the sample inlet 4 and the feeding box 8 is opened. The actuator arm 9 returns to the feeding box 8, the interface between the sample inlet and the feeding box 8 is closed, and the vacuum environment is created in the feeding box 8. The first GaN reaction chamber 2A is opened, the actuator arm 9 places the graphite tray 11 with the substrate 10 into the first GaN reaction chamber 2A, the actuator arm 9 exits from the first GaN reaction chamber 2A, and the first GaN reaction chamber 2A is sealed. Therefore, one circulation is completed in the first GaN reaction chamber 2A.
[0065] Upon completion of the first circulation, the first GaN reaction chamber 2A is preheated again at 500° C. after 1 h, and injected with the gas for second circulation. Subsequent circulation is executed at the time interval of 1 h.
[0066] After 2.5 h of the first circulation of the first GaN reaction chamber 2A, the second GaN reaction chamber 2B is preheated and injected with the gas. After 5 h of the first circulation of the first GaN reaction chamber 2A, the third GaN reaction chamber 2C is preheated and injected with the gas. Both the second GaN reaction chamber 2B and the third GaN reaction chamber 2C enter new circulation after 1 h upon completion of the reaction.
[0067] In first circulation, the ZnO reaction chamber 3 is preheated and injected with the gas for the first time after 0.5 h upon completion of the growth in the first GaN reaction chamber 2A, preheated and injected with the gas for the second time after 0.5 h upon completion of the growth in the second GaN reaction chamber 2B, and preheated and injected with the gas for the third time after 0.5 h upon completion of the growth in the third GaN reaction chamber 2C. After 2 h, the growth in the ZnO reaction chamber is completed. The actuator arm 9 takes out the graphite tray 11, both the actuator arm 9 and the graphite tray 11 are located in the feeding box 8, and the gas in the feeding box is extracted to create the vacuum environment. The interface between the sample outlet 5 and the feeding box 8 is opened, the actuator arm 9 feeds the graphite tray 11 to the sample outlet 5, the chip grown completely is taken out through the sample outlet 5 and fed to the outside, and the graphite tray 11 still remains on the actuator arm 9. After the finished chip is taken out, the actuator arm 9 brings the graphite tray 11 back to the feeding box 8. The graphite tray baking furnace 7 is opened, the actuator arm 9 feeds the graphite tray 11 to the graphite tray baking furnace 7, the actuator arm 9 returns to the feeding box 8, and the graphite tray baking furnace 7 is closed. The graphite tray baking furnace 7 is heated, until GaN and ZnO residues on the graphite tray 11 are vaporized. The graphite tray baking furnace 7 discharges vaporized gas, and the graphite tray 11 becomes clean again. The graphite tray baking furnace 7 is opened, and the actuator arm 9 takes out the graphite tray 11. The graphite tray baking furnace 7 is closed, the sample inlet 4 is opened, the actuator arm 9 feeds the graphite tray 11 to the sample inlet 7, and the actuator arm 9 returns to the feeding box 8, thereby completing the first circulation of the ZnO reaction chamber, and entering second circulation. With the manner in which the graphite tray is taken out and fed to the furnace automatically, the labor cost can be reduced effectively.
[0068] The annealing furnace 6 is intended to eliminate the residual stress of the GaN epi-wafer, reduce the deformation and cracking of the GaN epi-wafer, refine the granularity, regulate the structure and remove the structural defects. There are mainly two annealing processes at present, including furnace annealing in the GaN reaction chamber, and furnace annealing with the graphite tray taken out and placed into the separate annealing furnace. The latter is employed in the embodiment. Specifically, at 6 h when the GaN epi-wafer on the graphite tray 11 in the first GaN reaction chamber 2A is grown completely, the actuator arm 9 transfers the graphite tray to the annealing furnace 6 to anneal for 1 min (the reference time is 20 s to 3 min, and the annealing time can be adjusted according to the specific process). Upon completion of the annealing, the actuator arm 9 transfers the graphite tray 11 to the ZnO reaction chamber for next reaction. As an added component, the annealing furnace 6 may be removed if the MOCVD machine has the furnace annealing function. Therefore,
[0069] Specifically, as shown in
[0070] After 6 h, the GaN epi-wafer is grown completely in the first GaN reaction chamber 2A, and the actuator arm 9 feeds the graphite tray 11, on which the GaN epi-wafer is grown completely, to the ZnO reaction chamber 3. At 6.5 h, the ZnO reaction chamber 3 starts to grow the ZnO thin film on the graphite tray 11 fed from the first GaN reaction chamber 2A, and the growth of the ZnO thin film is completed at 8.5 h. At 9 h, the ZnO reaction chamber 3 starts to grow the ZnO thin film on the graphite tray 11 fed from the second reaction chamber 2B, and the growth of the ZnO thin film is completed at 11 h. At 11.5 h, the ZnO reaction chamber 3 starts to grow the ZnO thin film on the graphite tray 11 fed from the third reaction chamber 2C, and the growth of the ZnO thin film is completed at 13.5 h, thereby completing one circulation. Whether the production is continued is determined according to actual requirements (the production is stopped if the production quantity meets the standard, or otherwise, next circulation and production is continued).
[0071] In case of the continuous production, the chip in the ZnO reaction chamber 3 is removed, and the substrate 10 is respectively supplemented to the vacant GaN reaction chamber 2A, GaN reaction chamber 2B and GaN reaction chamber 2C, to enter next circulation and produce the finished chip products continuously.
[0072] For those of ordinary skilled in the art, certain simple modifications or substitutions may be made without departing from the concept of the present disclosure, which does not involve any inventive efforts. Therefore, simple improvements made to the present disclosure by those skilled in the art according to disclosures of the present disclosure should be included in the protection scope of the present disclosure. The above embodiments are preferred embodiments of the present disclosure. Any processes similar to the present disclosure and equivalent changes should be included in the protection scope of the present disclosure.