The present application is based upon and claims the benefit of priority of Japanese patent application No. 2010-219197, filed on Sep. 29, 2010, the entire contents of which are incorporated by reference in their entirety.
1. Field of the Present Disclosure
The present disclosure relates to a film deposition device and a film deposition method which are adapted to deposit a film on a substrate in a chamber by performing a number of cycles of sequentially supplying at least two kinds of mutually reactive gases to the substrate to laminate layers of resultants of the reactive gases on the substrate.
2. Description of the Related Art
As one of fabrication processes of semiconductor integrated circuits (ICs), there is a film deposition method called Atomic Layer Deposition (ALD) or Molecular Layer Deposition. This film deposition method may be carried out in a turntable type ALD device. An example of such an ALD device has been proposed by the applicant of this patent application. See Patent Document 1 listed below.
The ALD device of Patent Document 1 is provided with a turntable that is arranged in a vacuum chamber and on which, for example, five substrates are placed, a first reactive gas supplying part that supplies a first reactive gas toward the substrates on the turntable, a second reactive gas supplying part that supplies a second reactive gas toward the substrates on the turntable and is arranged away from the first reactive gas supplying part in the vacuum chamber. In addition, the vacuum chamber includes a separation area that separates a first process area in which the first reactive gas is supplied from the first reactive gas supplying part and a second process area in which the second reactive gas is supplied from the second reactive gas supplying part. The separation area includes a separation gas supplying part that supplies a separation gas and a ceiling surface that creates a thin space with respect to the turntable thereby to maintain the separation area at a higher pressure than the pressures in the first and the second process areas with the separation gas from the separation gas supplying part.
With such a configuration, because the first and the second process areas are kept at a sufficiently high pressure, the first reactive gas and the second reactive gas can be impeded from being intermixed in the vacuum chamber, even when the turntable is rotated at a high rotational speed, thereby improving production throughput.
Patent Document 1: Japanese Laid-Open Patent Publication No. 2010-56470
Improvement of the production throughput of ALD is increasingly demanded. In order to meet the demand, it is useful to increase the rotational speed of the turntable. However, if the rotational speed of the turntable is increased, the reactive gases will be easily intermixed by the high-speed rotation of the turntable. There is a trade-off relationship between raising the rotational speed of the turntable and improving the production throughput.
In one aspect, the present disclosure provides an atomic layer (molecular layer) film deposition device and method which can separate the reactive gases from each other certainly.
In another aspect, the present disclosure provides a film deposition device that supplies at least two kinds of mutually reactive gases sequentially to a substrate disposed in a chamber and laminates layers of resultants of the reactive gases on the substrate to deposit a film thereon, the film deposition device including: a turntable that is rotatably arranged in the chamber and includes a substrate receiving area in which the substrate is placed; a first reactive gas supplying portion that is arranged in a first area in the chamber to extend in a direction transverse to a rotation direction of the turntable and supplies a first reactive gas toward the turntable; a second reactive gas supplying portion that is arranged in a second area located in the chamber apart from the first area in the rotation direction of the turntable, to extend in a direction transverse to the rotation direction of the turntable, and supplies a second reactive gas toward the turntable; a first exhaust port that is arranged to communicate with the first area; a second exhaust port that is arranged to communicate with the second area; a separation gas supplying portion that is arranged between the first area and the second area and supplies a separation gas for separating the first reactive gas and the second reactive gas in the chamber; a convex part that is arranged to include a ceiling surface that covers both sides of the separation gas supplying portion and forms a first space between the ceiling surface and the turntable where the separation gas flows, the convex part being arranged to form a separation area between the first area and the second area, the separation area being arranged to maintain a pressure in the first space to be higher than pressures in the first area and the second area so that the first reactive gas from the first area and the second reactive gas from the second area are separated by the separation gas in the separation area; and a block member that is arranged between the turntable and an internal surface of the chamber in the separation area to form a second space between the turntable and the internal surface of the chamber at an upstream part of the separation area along the rotation direction of the turntable.
In another aspect, the present disclosure provides a film deposition method that performs a film deposition process for a substrate placed in the substrate receiving area of the turntable in the above-described film deposition device, the film deposition method including: supplying, by the separation gas supplying portion, the separation gas; supplying, by the first reactive gas supplying portion, the first reactive gas, and supplying, by the second reactive gas supplying portion the second reactive gas; and passing the separation gas through the second space between the turntable and the internal surface of the chamber in the upstream part of the separation area along the rotation direction of the turntable.
The aspects and advantages of the present disclosure will be realized and attained by means of the elements and combinations particularly pointed out in the claims. It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory and are not restrictive of the present disclosure as claimed.
A description will now be given of non-limiting, exemplary embodiments of the present disclosure with reference to the accompanying drawings. In the drawings, the same or corresponding reference numerals or letters are given to the same or corresponding members or components. It is noted that the drawings are illustrative of the present disclosure, and there is no intention to indicate scale or relative proportions among the members or components. Therefore, the specific size should be determined by a person having ordinary skill in the art in view of the following non-limiting embodiments.
Referring to
As shown in
As shown in
As shown in
The rotary shaft 22 and the driving device 23 are housed in a cylindrical case body 20 having an open top surface. The case body 20 is airtightly attached to the back surface of the bottom of the vacuum chamber 10 via a flange part 20a provided in the top surface of the case body 20, so that an internal atmosphere of the case body 20 is isolated from an external atmosphere.
Referring back to
Hereinafter, the convex part 4B will be described. Because the convex part 4A and the convex part 4B have the same structure, a duplicate description of the convex part 4A will be omitted.
As shown in
In the following, the separation gas nozzle 41 and the separation gas nozzle 42 will be referred to as the separation gas nozzle 41 (42). The separation gas nozzle 41 (42) is connected to a gas supplying source (not shown) of a separation gas. The separation gas may be an inert gas, such as nitrogen (N2) gas. The kind of the separation gas will not be limited to the inert gas. Alternatively, the separation gas may be any gas that does not affect the film deposition. In this embodiment, N2 gas is used as the separation gas.
The separation gas nozzle 41 (42) has discharge holes 41h for discharging the N2 gas to the surface of the turntable 2 (
As shown in
On the other hand, a first area 481 and a second area 482 that are defined by the top surface of the turntable 2 and the bottom surface of ceiling plate 11 are formed on the respective sides of the convex part 4B. The heights (or heights of the bottom surface of the ceiling plate 11 from the top surface of the turntable 2) of the first and second areas 481,482 may be in a range of 15 mm-150 mm, which are larger than the height of the separation space H. A reactive gas nozzle 31 is provided in the first area 481, and a reactive gas nozzle 32 is provided in the second area 482. As shown in
The reactive gas nozzles 31 and 32 are located apart from the bottom surface of the ceiling plate 11, as shown in
A first reactive gas is supplied from the reactive gas nozzle 31, and a second reactive gas is supplied from the reactive gas nozzle 32. In this embodiment, a gas supplying source of bis(tertiary-butylamino)silane (BTBAS) which is a silicon source material of a silicon oxide film is connected to the reactive gas nozzle 31. A gas supplying source of gaseous ozone (O3) as an oxidizing gas which oxidizes BTBAS to produce silicon oxide is connected to the reactive gas nozzle 32.
The reactive gas nozzle 31 is an example of the first reactive gas supplying portion that is arranged in the first area 481 in the vacuum chamber 10 to extend in a direction transverse to the rotation direction A of the turntable 2 and supplies the first reactive gas toward the turntable 2. The reactive gas nozzle 32 is an example of the second reactive gas supplying portion that is arranged in the second area 482 located in the vacuum chamber 10 apart from the first area 481 in the rotation direction A of the turntable 2, to extend in a direction transverse to the rotation direction A of the turntable 2, and supplies the second reactive gas toward the turntable 2. The separation gas nozzle 41 and the separation gas nozzle 42 are an example of the separation gas supplying portion that is arranged between the first area 481 and the second area 482 and supplies the separation gas for separating the first reactive gas and the second reactive gas in the vacuum chamber 10. The convex part 4A and the convex part 4B are an example of the convex part that is arranged to include the ceiling surface that covers both sides of the separation gas supplying portion and forms the first space between the ceiling surface and the turntable 2 where the separation gas flows, the convex part being arranged to form a separation area between the first area 481 and the second area 482, the separation area being arranged to maintain a pressure in the first space to be higher than pressures in the first and second areas so that the first reactive gas from the first area 481 and the second reactive gas from the second area 482 are separated by the separation gas in the separation area.
When nitrogen (N2) gas is supplied from the separation gas nozzle 41, the N2 gas flows to the first area 481 and the second area 482 from the separation space H. As described above, the height h1 of the separation space H is smaller than the heights of the first and second areas 481,482, a pressure of the separation space H can be easily maintained to be higher than the pressures of the first and second areas 481,482. In other words, the height and width of the convex part 4B and a flow rate of the N2 gas from the separation gas nozzle 41 are preferably determined so that the pressure of the separation space H can be easily maintained to be higher than the pressures of the first and second areas 481,482. When the flow rates of BTBAS gas and O3 gas are determined, the rotational speed of the turntable 2 and the like are preferably taken into consideration. In this manner, the separation space H can provide a pressure wall against the first and second areas 481,482, thereby certainly separating the first area 481 and the second area 482.
Specifically, as shown in
According to the analyses of the inventors of the present disclosure, with the above-described structure, it is possible to certainly separate BTBAS gas and O3 gas from each other even when the turntable 2 is rotated at a rotational speed of about 240 rpm.
Referring back to
Furthermore, a separation gas supplying pipe 51 is connected to the upper center of the ceiling plate 11 and supplies N2 gas. With this N2 gas supplied from the separation gas supplying pipe 51, the space between the core portion 21 and the ceiling plate 11, the space between the outer circumferential surface of the core portion 21 and the inner circumferential surface of the projecting portion 5, and the space between the projecting portion 5 and the turntable 2 can have a higher pressure than the pressures of the first and second areas 481,482. Incidentally, these spaces will be referred to as a center space. This center space can provide a pressure wall against the first and second areas 481,482, thereby certainly separating the first and second areas 481,482 from each other. Namely, it is possible to effectively prevent the BTBAS gas and the O3 gas from being intermixed through the center space.
As shown in
The exhaust port 61 is positioned between the reactive gas nozzle 31 and the convex part 4B located downstream relative to the reactive gas nozzle 31 along the rotation direction A of the turntable 2. The exhaust port 62 is positioned between the reactive gas nozzle 32 and the convex part 4A located downstream relative to the reactive gas nozzle 32 along the rotation direction A of the turntable 2. Hence, the BTBAS gas supplied from the reactive gas nozzle 31 is exhausted through the exhaust port 61, and the O3 gas supplied from reactive gas nozzle 32 is exhausted through the exhaust port 62. The arrangement of the exhaust ports 61 and 62 contributes to separation of the two reactive gases.
The exhaust port 61 is an example of the first exhaust portion arranged to communicate with the first area 481. The exhaust port 62 is an example of the second exhaust portion arranged to communicate with the second area 482.
As shown in
As shown in
Near the lower circumferential part of the turntable 2, a lower block member 71 is arranged to surround the heater unit 7. Hence, the space in which the heater unit 7 is placed is separated from the outside area of the heater unit 7 by the lower block member 71. In order to prevent the gas from flowing to the inside of the lower block member 71, a small gap is arranged between the top surface of the lower block member 71 and the bottom surface of the turntable 2. In order to purge this area, two or more purge gas supplying pipes 73 are arranged at a predetermined spacing and connected to the area in which the heater unit 7 is accommodated to penetrate the bottom of the chamber body 12.
As shown in
With the above structure, N2 gas supplied from the above-mentioned purge gas supplying pipe 73 fills the space formed between the protective plate 7a and the lower block member 71, flows from the gaps 7g between the raised part R and the protective plate 7a into the space between the turntable 2 and the protective plate 7a, and is exhausted through the space from the exhaust ports 61 and 62. Thereby, BTBAS gas and O3 gas can be prevented from entering the space in which the heater unit 7 is accommodated, so that the heater unit 7 can be protected. The N2 gas as described above functions as separation gas which prevents the BTBAS gas and the O3 gas from being intermixed through the space of the lower part of the turntable 2.
Alternatively, two or more slots may be formed in a portion of the lower block member 71 near the openings corresponding to the exhaust ports 61 and 62, and the gaps equivalent to the gaps 7g may be provided. With this structure, the N2 gas supplied from the purge gas supplying pipe 73 is exhausted through the space in which the heater unit is accommodated to the exhaust ports 61 and 62. In this manner, it is also possible to prevent the BTBAS gas and the O3 gas from entering the space in which the heater unit 7 is accommodated.
As shown in
With this structure, the N2 gas from the purge gas supplying pipe 72 passes through the gap between the rotary shaft 22 and the central hole on the bottom of the chamber body 12, the gap between the core portion 21 and the raised part R on the bottom of the turntable 2, and the gap between the raised part R and the bottom surface of the turntable 2. The N2 gas flows through the space between the turntable 2 and the protective plate 7a, and is exhausted through the exhaust ports 61 and 62. Hence, the N2 gas from the purge gas supplying pipe 72 functions as separation gas which prevents the BTBAS gas and the O3 gas from being intermixed through the space of the lower part of the turntable 2.
As shown in
The upper block member 46B substantially fills the space between the turntable 2 and the chamber body 12, prevents the BTBAS gas from the reactive gas nozzle 31 from entering the space to flow from the first area 481 into the second area 482, and prevents intermixing of the BTBAS gas and the O3 gas. For example, the gap between the upper block member 46B and the chamber body 12 and the gap between the upper block member 46B and the turntable 2 may have a height that is the same as the height h1 of the ceiling surface 44 of the convex part 4 from the turntable 2. Because of the use of the upper block member 46B, it is possible to prevent the N2 gas from the separation gas nozzle 41 (
It is preferred to set the gap between the upper block member 46B (46A) and the turntable 2 to be the same as the above-described spacing (h1), in consideration of the thermal expansion of the turntable 2 when the turntable 2 is heated by the heater unit.
The upper block member 46B (46A) is an example of the block member arranged between the turntable 2 and the internal surface of the vacuum chamber 10 in the separation area to form a second space between the turntable 2 and the internal surface of the vacuum chamber 10 at an upstream part of the separation area along the rotation direction A of the turn table 2.
When the turntable 2 is rotated in the direction indicated by the arrow A in
As shown in
As shown in
The memory device 100c is constructed to store the control programs which cause, when executed, the process controller 100a to perform various processes, the process recipe, the parameters of the various processes, etc. The control programs include a set of code instructions for causing the process controller 100a to execute the film deposition method according to the present disclosure. According to a command from the user interface part 100b, the control programs and the process recipes are read from the memory device and loaded to the internal memory by the process controller 100a, and executed by the control unit 100. These programs may be stored in a computer-readable storage medium 100d, and may be installed in the memory device 100c through an input-output interface (not shown) of the film deposition device 1. The computer-readable storage medium 100d may be a hard disk, a CD, a CD-R/RW, a DVD-R/RW, a flexible disk, a semiconductor memory, etc. Moreover, the programs may be downloaded to the memory device 100c through a communication network.
Next, operation (the film deposition method) of the film deposition device of this embodiment will be described. First, the turntable 2 is rotated so that one of the substrate receiving areas 24 is aligned to the conveyance opening 15, and the gate valve 15a is opened.
Next, the wafer W is conveyed to the vacuum chamber 10 through the conveyance opening 15 by the conveyance arm 10A, and held above the substrate receiving area 24.
Subsequently, the wafer W is disposed in the substrate receiving area 24 by the collaborating operation of the conveyance arm 10A and a lifting/lowering pin (which is not shown) which is arranged to be lifted or lowered in the substrate receiving area 24. The above-described operation is repeated 5 times, so that five wafers W are disposed in the five substrate receiving areas 24 of the turntable 2 respectively. Then, the gate valve 15a is closed and the conveyance of the wafers W is completed.
Next, the inside of the vacuum chamber 10 is exhausted by the exhaust device 64, while the N2 gas is supplied from the separation gas nozzles 41 and 42, the separation gas supplying pipe 51, and the purge gas supplying pipes 72 and 73, so that the vacuum chamber 10 is maintained at a predetermined pressure by the pressure regulator 65.
Subsequently, the turntable 2 starts rotating in a clockwise direction when viewed from the top surface. The turntable 2 is heated at a predetermined temperature (for example, 300 degrees C.) in advance by the heater unit 7, and thus the wafers W on the turntable 2 are heated at the same temperature.
After the wafers W are heated and maintained at the predetermined temperature, the BTBAS gas is supplied to the first area 481 from the reactive gas nozzle 31, and the O3 gas is supplied to the second area 482 from the reactive gas nozzle 32. In this situation, the BTBAS gas from the reactive gas nozzle 31 (
On the other hand, the O3 gas from the reactive gas nozzle 32 is exhausted through the exhaust port 62 together with the N2 gas which flows from the separation gas nozzle 42 to the second area 482 through the separation space between the convex part 4B and the turntable 2, the N2 gas which flows from the separation gas supplying pipe 51 to the second area 482 through the space between the core portion 21 and the turntable, and the N2 gas which flows from the separation gas nozzle 41 to the second area 482 through the separation space between the convex part 4A and the turntable 2.
When the wafers W pass through the lower part of the reactive gas nozzle 31, the BTBAS molecules are adsorbed to the surfaces of the wafers W. When the wafers W pass through the lower part of the reactive gas nozzle 32, the adsorbed BTBAS molecules on the surfaces of the wafers W are oxidized by the O3 molecules. Therefore, each time the wafer W passes through the first area 481 and the second area 482 by the rotation of the turntable 2, one molecular layer (or two or more molecular layers) of silicon oxide is formed on the surface of the wafer W. This process is repeated and a silicon oxide film having a predetermined thickness is deposited on the surface of the wafer W.
After the silicon oxide film having the predetermined thickness is deposited, the supply of BTBAS gas and O3 gas is stopped and the rotation of the turntable 2 is stopped. The wafers W are taken out from the vacuum chamber 10 by the conveyance arm 10 by performing the operation contrary to the conveyance operation, so that the film deposition process is completed.
In the film deposition device of this embodiment, the height h1 of the separation space H between the convex part 4A or 4B and the turntable 2 (
In the film deposition device of this embodiment, the reactive gas nozzles 31 and 32 are positioned near the top surface of the turntable 2 and apart from the ceiling plate 11 (refer to
In the film deposition device of this embodiment, the upper block members 46A and 46B are arranged in the lower parts of the convex parts 4A and 4B and between the turntable 2 and the inner circumferential wall of the chamber body 12, N2 gas from the separation gas nozzles 41 and 42 hardly flows into the space between the turntable 2 and the inner circumferential wall of the chamber body 12, and it is possible to maintain the pressure in the separation space H at a high pressure.
Next, the advantages of the space S of the lower part of the convex parts 4A and 4B will be described with reference to
For comparison purposes,
On the other hand, O3 gas supplied to the second area 482 from the reactive gas nozzle 32 (refer to
On the other hand, as shown in
As shown in
The present disclosure is not limited to the above-described embodiments, and variations and modifications may be made without departing from the scope of the present disclosure.
For example, a convex part 40A shown in
As shown in
In the example shown in
However, it is not necessary to form the auxiliary portion 4a. In a case in which the auxiliary portion 4a is not formed, the space S is formed by the bottom surface of the ceiling plate 11, the inner circumferential wall of the chamber body 12, and the outer circumferential wall of the turntable 2. In
Alternatively, the protective plate 7a may be provided so that it does not extend to the lower part of the convex parts 4A and 4B (that is, the outer circumferential wall of the protective plate 7a matches with the outer circumferential wall of the turntable 2), and the upper block member may be disposed on the lower block member 71. Moreover, in this case, the upper block member which extends to the bottom surface (or the bottom surface of the ceiling plate 11) of the convex parts 4A and 4B from the bottom of the chamber body 12 may be provided without providing the lower block member 71 in the lower portion of the convex parts 4A and 4B. In any case, the space S has to be formed.
In the foregoing embodiments, the slot 43 of the convex part 4A or 4B is formed to bisect the convex part 4A or 4B. Alternatively, the slot 43 may be formed in a downstream side of the convex part 4A or 4B so that the ceiling surface 44 (or the bottom surface of the convex part 4A or 4B) is enlarged in an upstream side thereof.
Alternatively, the reactive gas nozzles 31 and 32 may be arranged to extend from the center portion of the vacuum chamber 10, instead of from the circumferential wall of the chamber body 12. Moreover, the reactive gas nozzles 31 and 32 may be arranged to extend at a predetermined angle with respect to the radial direction of the turntable 2.
In addition, a length of the convex parts 4A and 4B, which is measured along the rotation direction of the turntable 2, may range from about 1/10 of the diameter of the wafer W to about 1/1 of the diameter of the wafer W, and it is desirable that the length of the convex parts 4A and 4B is about 1/6 or more of the diameter of the wafer W in terms of an arc that corresponds to a path through which the center of the wafer passes. With this structure, it is possible to easily maintain the separation space H at a high pressure.
The film deposition device of the present disclosure is applicable to ALD (or MLD) film deposition of a silicon nitride film. In addition, the film deposition device of the present disclosure is applicable to ALD (or MLD) film deposition of an aluminum oxide film using trimethyl aluminum (TMA) gas and O3 gas, a zirconium oxide film using tetrakis-ethyl-methyl-amino-zirconium (TEMAZr) gas and O3 gas, a hafnium oxide film using tetrakis-ethyl-methyl-amino-hafnium (TEMAH) gas and O3 gas, a strontium oxide film using bis(tetra methyl heptandionate) strontium (Sr(THD)2) gas and O3 gas, a titanium oxide film using (methyl-pentadionate)(bis-tetra-methyl-heptandionate) titanium (Ti(MPD)(THD)) gas and O3 gas, or the like. In addition, O2 plasma may be used instead of the O3 gas. Moreover, combinations of any gases described above may be used.
As described in the foregoing, according to the foregoing embodiments of the present disclosure, it is possible to provide an atomic layer (molecular layer) film deposition device and method which can separate the reactive gases from each other certainly.
Number | Date | Country | Kind |
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2010-219197 | Sep 2010 | JP | national |