The present disclosure relates to atomic layer deposition, and in particular relates to atomic layer deposition systems and methods having high throughput.
The entire disclosure of any publication or patent document mentioned herein is incorporated by reference, including U.S. Pat. Nos. 5,997,963; 6,066,210; 7,833351; 8,877,300; and U.S. Patent Application Publications No. US 2010/00183825 and US 2013/0196078.
Atomic layer deposition (ALD) is a method of depositing a thin film on a substrate in a very controlled manner. The deposition process is controlled by using two or more chemicals in vapor form (i.e., “process gasses”) and reacting them sequentially and in a self-limiting manner on the surface of the substrate such as a silicon wafer. The sequential process is repeated to build up the thin film layer by layer, wherein the layers are atomic scale.
ALD is used to form a wide variety of films, such as binary, ternary and quaternary oxides for advanced gate and capacitor dielectrics, as well as metal-based compounds for interconnect barriers and capacitor electrodes.
The ALD process can be carried out in a single chamber system, as is well known in the art. However, the ALD process is relatively slow as compared to for example chemical vapor deposition and like processes. The typical ALD process introduces a first process gas into the single process chamber. The sample sits in this environment for a short period of time to expose the surface to the first process gas. Typically, less than 1 sec is required for this step, and it has been shown that only a few milliseconds are actually required.
Once the surface is saturated with the first process gas, the first process gas is pumped out of the chamber. Then an inert or purge gas is flowed through the chamber. Then a second process gas is introduced into the chamber. The second process gas reacts with the surface of the substrate that was saturated by the first process gas. The purpose of the inert gas flowing through the chamber before the second process gas is flowed into the chamber is to ensure that all of the original unreacted process gas is removed. The second process gas reacts with the surface of the substrate that was saturated with the first process gas. Once this second reaction process is completed (in a few milliseconds), the second process gas is removed and the chamber is again purged with an inert gas. Then, the first process gas is introduced into the chamber and the entire reaction sequence is repeated until an ALD film of a desired thickness is obtained.
The basic reason why an ALD process is slow is not related to the reaction rate of the process gasses at the substrate surface. This reaction is relatively quick. The ALD process takes a long time because of the time required to flow process gas into the chamber, pump out the process gas, flow inert gas, pump out the inert gas, then flow the next process gas into the chamber, etc. It is the flow mechanics that limit the throughput of the ALD and not the reaction rates. Each deposition sequence usually takes several seconds, and an entire cycle can take minutes.
Furthermore, the primary reason why the ALD process is expensive is that each ALD layer that makes up the ALD film consumes relatively large quantities of expensive process gasses. Typically, the reaction chamber is much larger than the substrate. With each cycle, the process gas is pumped out. The actual utilization of the process gases in the ALD reactions is typically a small fraction of 1%.
To speed up the ALD process, multiple ALD chambers can be used. Alternatively, a large chamber that contains multiple substrates can be used to perform what is known as batch processing. Either way, speeding up the ALD process to increase the throughput of substrates translates into reduced cost per substrate. In addition, simplification of the ALD systems can also be used to reduced costs. In particular, reducing the cost of ownership of the ALD system (and in particular, a multichamber ALD system) can be used to reduce the cost per substrate.
Consequently, there is a need for improved ALD systems and methods that increase throughput while avoiding complexity that adds to the system costs and to the production costs.
The present disclosure is directed to ALD systems and methods that simplify the ALD process while also reducing the cost of the ALD process by reducing the amounts of process gasses used. Aspects of the ALD systems and methods include containing the process gases within separate process sections of a process chamber and moving the substrate between the separate chamber sections without having to remove the gases from the chamber sections.
An aspect of the disclosure is a process chamber for a multichamber ALD system for performing ALD on multiple wafers. The process chamber includes: a housing having an interior divided into multiple chamber sections by chamber dividers disposed within the housing interior, the housing having an open bottom end; a rotatable platen having a central axis and an upper surface that supports the multiple wafers and that is operably disposed with its upper surface adjacent the bottom end of the housing and spaced apart therefrom by a gap, wherein the platen is rotatable to move the wafers between the multiple chamber sections; and a pneumatic valve operably disposed in each chamber divider, wherein each pneumatic valve is in pneumatic communication with the platen surface within the gap and forms a pneumatic partition between adjacent chamber sections.
Another aspect of the disclosure is a multichamber ALD system that includes the the process chamber disclosed herein and as described above; a process gas system operably connected to at least two of the chamber sections; and a purge gas system operably connected to at least two of the chamber sections different than the two chamber sections operably connected to the process gas system.
Another aspect of the disclosure is a method of performing ALD on multiple wafers each having a surface to form an ALD film on each of the wafers. The method includes: supporting the multiple wafers on a surface of a platen that is spaced apart from a process chamber housing by a gap G that is 500 microns or less, wherein the process chamber includes multiple chamber sections; pneumatically partitioning the process chamber sections; rotating the platen beneath the process chamber housing, thereby causing the wafers to move between the chamber sections; and performing an ALD process in at least one of the chambers sections as the wafers pass through the chamber sections to form the ALD film.
Other aspects of the method include performing at least one of laser processing and plasma processing of the wafers in one or more of the chamber sections. The rotation rate of the platen is limited only by the reaction rates of the particular process gasses with the wafer surface or the ALD film layer formed on the wafer surface during each full platen rotation.
Additional features and advantages are set forth in the Detailed Description that follows, and in part will be readily apparent to those skilled in the art from the description or recognized by practicing the embodiments as described in the written description and claims hereof, as well as the appended drawings. It is to be understood that both the foregoing general description and the following Detailed Description are merely exemplary, and are intended to provide an overview or framework to understand the nature and character of the claims.
The accompanying drawings are included to provide a further understanding, and are incorporated in and constitute a part of this specification. The drawings illustrate one or more embodiment(s), and together with the Detailed Description serve to explain principles and operation of the various embodiments. As such, the disclosure will become more fully understood from the following Detailed Description, taken in conjunction with the accompanying Figures, in which:
Reference is now made in detail to various embodiments of the disclosure, examples of which are illustrated in the accompanying drawings. Whenever possible, the same or like reference numbers and symbols are used throughout the drawings to refer to the same or like parts. The drawings are not necessarily to scale, and one skilled in the art will recognize where the drawings have been simplified to illustrate the key aspects of the disclosure.
The claims as set forth below are incorporated into and constitute part of this Detailed Description.
Cartesian coordinates are shown in some of the Figures for the sake of reference and are not intended to be limiting as to direction or orientation.
In the discussion below, a “process gas” may be constituted by one or more gas constituents or may consist of a single gas constituent. A process gas is one that is reactive with the surface of a substrate (wafer), including an ALD film layer that is formed on the wafer surface.
Also in the discussion below, a “purge gas” is a non-reactive gas such nitrogen or one or more other inert gasses that do not react in any substantial way with the wafer surface or an ALD film layer that is formed on the wafer surface.
The phrase “between P and Q” as used below where P and Q are numerical values includes the values P and Q.
In the discussion below, a full rotation of the platen is one where the platen rotation starts from an initial position and returns to the initial position, i.e., the platen rotates 360 degrees.
In the discussion below, two process gasses 111 and 112 are discussed by way of example. When referring generally to a “process gas,” the reference number 111 is used for convenience, and it will be understood that such reference can also apply to the other process gas 112 or additional process gases.
Multichamber ALD System
The housing 30 of process chamber 20 includes an interior 40 having a height (“interior height”) H as measured between top and bottom ends 34 and 36 of housing 30. The interior 40 includes dividers 44 that in an example radially extend from housing axis AH.
As discussed below, system 10 is configured to process multiple wafers 70 having a thickness THW and a diameter or width Wd. In an example, the interior height H can be selected so that interior chamber sections 41 use relatively small amounts of process gas or purge gas when processing wafers 70. In an example, the interior height H is in the range 5·THW≦H≦100·THW or 10·THW≦H≦50·THW or 10·THW≦H≦20·THW. Thus, for an example wafer thickness THW=750 microns, an example interior height can be between about 1 cm and 5 cm.
Process chamber 20 also includes a rotatable platen 60.
Platen 60 is arranged adjacent bottom end 36 of housing 30 and spaced apart therefrom in the z-direction to define a gap G. In an example, the gap G is in the range from 50 microns to 500 microns. In an example, gap G<1 mm. In an example, upper surface 62 of platen 60 includes recesses 63 each sized to accommodate a wafer 70 so that the wafer surface 72 resides at or below the upper surface of the platen (See
The platen radius R needed to support n wafers of diameter Wd can be approximated by the equation:
R=(n)·(Wd)/(2π)+(Wd/2)
In an example, platen 60 is configured to heat wafers 70 to up to 400° C. to facilitate the ALD process. This heating capability can be achieved, for example, by one or more heating elements 64 operably arranged either within or in thermal contact with platen 60, as shown in
With reference again to
With reference also to
System 20 also includes a purge gas system 130 that is operably connected to process chamber 20. The purge gas system 130 includes a purge gas supply 132 that contains a purge gas 142, such as nitrogen or another inert gas. In the example shown in
System 10 also includes a vacuum system 160 operably connected to pneumatic valves 50 in dividers 44 via vacuum lines 162.
The chamber sections 41 can be kept at a substantially constant pressure, i.e., they need not have their particular gas pumped out and then added back again as is done in conventional ALD systems. Rather, the gas remains in the given chamber section 41 and the wafers are moved into the different chambers sections via the rotation of platen 60 beneath housing 30. This also creates a slight pressure differential with respect to the pneumatic valves 50 that reside between the chamber sections. In one example, this pressure differential is “negative” encourages the flow of gas into the gaps G under dividers 44 and into the pneumatic valves, which substantially prevents the flow of gas to the adjacent chamber section by creating gas curtain between chamber sections. In another example, the pressure differential is “positive” so that flow of purge gas from the pneumatic valves 50 discourages the flow of gas in the adjacent chamber sections 41 into the corresponding gap G under divider 44.
Because the process gases 101, 102, etc. remain in their respective chamber sections 41 rather than being pumped out between process steps, system 10 substantially reduces the cost of the ALD deposition process. As noted above, a large portion of the ALD process cost is associated with the process gas. In prior art systems, a chamber for a 200 mm wafer and that has a 10 mm chamber height occupies approximately 500 cm3 and the gas pressure is nominally 100 millitorr. For each ALD film layer, all the process gas is pumped out and replaced. For a 1000 layer pair, 2×500 cm3×1000×100 millitorr=105 cm3-torr of expensive gas is consumed. In system 10 and the related methods disclosed herein, the volume of a chamber section 41 is filed once so that about 1000 times less process gas is consumed.
With reference again to
System 20 further includes a controller 180 operably connected to process gas system 100, purge gas system 130 and vacuum system 160 and drive motor 170. Controller 180 is generally configured to control the operation of system 10, e.g., by instructions embodiment in a non-transitory computer-readable medium 182 within or operably connected to the controller.
Process chamber 20 is configured such that each chamber section 41 contains a particular gas, e.g., a particular process gas or a purge gas. The pneumatic valve 50 and the purge gas channels 252 and vacuum channels 262 therein are configured to pneumatically isolate adjacent chamber sections 41. Each pneumatic valve 50 is in pneumatic communication with the upper surface 62 of platen 60 through gap G and forms a pneumatic partition between adjacent chamber sections 51.
To accomplish this pneumatic partitioning, in one example each pneumatic valve 50 includes at least two vacuum channels 262 that respectively reside closest to the sides 45 of divider 44, and also includes at least one purge channel 252 that resides between the two vacuum channels (i.e., the two vacuum channels sandwich the at least one purge channel). This pneumatic configuration can be described from left to right as “V-P-V,” where “V” stands for vacuum and “P” stands for purge (see
While it is preferable that then pneumatic partitioning between adjacent chamber sections 41 be as robust as possible, it is noted here that it need not be perfect. In an example, some process gas from one chamber section 41 can migrate to the adjacent chamber section, and some purge gas can migrate from one chamber section to the adjacent chamber section, as long as the amount of migrating gas involved is insubstantial. Here, insubstantial means that it does not substantially alter the ALD process that occurs within the given chamber section 41, i.e., does not substantially affect the quality of the final ALD film 74 being formed. If relative few atoms of gas migrate from one chamber section to another as compared to the amount of gas that is already in the chamber section. the impact on the formation of the final ALD film will be insubstantial.
The example configuration of the pneumatic valve 50 shown in
The basic V-P-V pneumatic configuration for pneumatic valve 50 (i.e., purge gas sandwiched by vacuum) allows for the purge gas 142 to flow through central purge gas channel 252 into gap G and spread out laterally only to be picked up a short distance later within the gap on each side of the purge gas channel by the adjacent vacuum channels 262. In addition, the outside “V” channels 262 respectively collect gas from their adjacent chamber section 41. In particular, the left-most vacuum channel 262 collects first process gas 111 from left-side chamber section 41 and that flows into gap G, while the right-most vacuum channel 262 collects purge gas 142 that resides within the right-side chamber section 41 and that also flows into gap G.
Likewise, the V-P-V-P-V-P-V of
Meanwhile, the innermost vacuum channels 262 respectively remove purge gas 142 from center purge gas channel 252 and the other adjacent purge gas channel. The downward flow of purge gas 142 under pressure in purge gas channels 252 and the upward flow of purge gas and process gas 111 under vacuum in vacuum channels 262 results in dynamic circulation of gasses that creates a gas buffer or “gas curtain” 55 that prevents the migration of substantial amounts of process gas and purge gas between adjacent chamber sections 41.
An alternate pneumatic configuration for pneumatic valve 50 is based on a P-V-P configuration, i.e., purge gas pressure P on the outside and vacuum V on the inside.
The general P-V-P configuration will typically allow some purge gas 142 to flow into the adjacent chamber sections 41. Here, the purge gas pressure P is substantially the same or slightly greater than the pressure in the adjacent chamber sections 41. In the case of one of the chamber sections 41 being a purge gas section, the migration of purge gas from pneumatic valve 50 into the purge gas chamber section is of no consequence. In the case where one of the chamber sections 41 contains a process gas, the amount of purge gas 142 that enters the process gas chamber section is insubstantial and thus has no substantial effect on the ALD process being carried out. On the other hand, the small amount of purge gas 142 that can migrate into the process gas chamber section 41 can serve to reduce or prevent the flow of process gas 111 into the pneumatic valve, i.e., can mitigate the loss of expensive process gas.
General Method of Operation
In the general operation of system 10, substrates 70 are disposed on the upper surface 62 of platen 60 and supported thereby, such as shown in
Since wafer surface 72 becomes saturated with process gas 111 in a matter of milliseconds, platen 60 can rotate fairly quickly. For example, if platen 60 rotates at 60 revolutions per minute (RPM) (i.e., 1 rotation per second), a wafer 70 will reside within each chamber section for a total of approximately 250 milliseconds (the “residence time”), which is sufficient to saturate the wafer surface 72. An example range on the rotation rate for platen 60 is between 10 RPM and 200 RPM or between 30 and 100 RPM.
In an example, the rotation rate of the platen 60 is such that the residence time of a wafer 70 in a given chamber section is between 100 milliseconds and 1000 milliseconds (i.e., 1 second), or between 200 milliseconds and 750 milliseconds, or between 250 milliseconds and 500 milliseconds. In an example, the residence time is measured from when the leading edge of the wafer 70 first enters the chamber section 41 until when the trailing edge of the wafer leaves the chamber section. It is noted that whatever non-uniform processing occurs by having a leading-edge portion of the wafer entering a given chamber section while the trailing edge remains outside of the chamber section is compensated by the non-uniform exposure to the trailing-edge portion of the wafer as the leading edge wafer leaves and resides outside of the given chamber section.
During the rotation of platen 60 and the attendant movement of wafers 70 between chamber sections 41, the pneumatic valves 50 in dividers 44 respectively serve as pneumatic partitions that pneumatically isolate adjacent chamber sections while allowing for a sufficient gap G for the wafers to move underneath housing 30 of chamber 20. As explained above, this pneumatic partitioning is accomplished by a combination of the flow of purge gas 142 under pressure via purge gas channels 252 and the judicious use of vacuum via vacuum channels 262 operably connected to vacuum system 160 via vacuum lines 162. As noted above, the pneumatic valve 50 creates gas curtain 55 that pneumatically isolates adjacent chamber sections 41.
The small amount of gas (process or purge) in a given chamber section 41 that is removed by the pneumatic valves 50 is replaced using the corresponding gas source to maintain the pressure in the chamber section. The amount of gas lost in this manner can be kept small by adjusting the vacuum levels and the flow of purge gas 142, and by keeping the gap G as small as possible. Also, as noted above, the consumption rate of process gas can be kept low or at a minimum by having a small or minimum size for gap G.
In an example, every other chamber sections 41 (e.g., 41A, 41C, . . . ) is a processing section while each intervening chamber section (e.g., 41B, 41D, . . . ) is a non-processing chamber section. In an example, processing chamber sections 41 contain gasses that are different than those in non-processing chamber sections. In an example, the primary purpose of non-processing chamber sections 41 are to separate the processing chamber sections and to provide transition locations where wafers 70 are prepared for the next process. In another embodiment, one or both of chamber sections 41B and 41D can also be configured as processing chamber sections.
An example ALD process that can be carried out in system 10 having four chamber sections 41 (41A through 41D) to form an AL2O3 film 74 is set forth in Table 1 below.
Another example ALD process that can be carried out in system 10 having four chamber sections 41 (41A through 41D) to form a GaN film is set forth in Table 2 below.
System 10 is not limited to a total of four chamber sections 41 as discussed in the examples above.
For example, adjacent processing chamber sections 41C and 41D can use similar process gasses with one of the chambers performing an additional processing action, such as heating, laser annealing, the addition of another process gas without purging the original process gas, etc. In another example, chamber 20 can have adjacent purge chamber sections 41, with one of the purge chamber sections also having laser-annealing capability such as described below.
In another example, two of the processing sections 41 can respectively use two different process gasses and the third processing section 41 can be used for another process, such as laser annealing, plasma processing, thermal processing, etc. Any reasonable number of chamber sections 41 can be used, e.g., 2 to 12 chamber sections or 3 to 8 chamber sections. A configuration of 4 (four) chamber sections 41 is anticipated to be particular useful because it allows for alternating process sections 41 separated by purge sections or other non-process-gas treatments, such as laser annealing, thermal treatment, etc.
Multichamber ALD System with Laser Annealing
Laser beam 312 is made incident upon wafer surface 72 or the ALD film 74 being formed therein. The chamber section 41 to which laser system 300 is operably arranged can be used to perform laser-enhanced ALD (“LE-ALD”). The laser system 300 can be operably arranged with respect to more than one chamber section 41 so that laser processing can be performed more than once for given cycle of wafer 70 through the chamber sections (i.e., multiple laser processing can be performed for each full rotation of platen 60). For example, in the four-chamber-section arrangement discussed above, the two purge chamber sections (say, 40B and 40D) can also be configured as LE-ALD process sections.
In an example, line image 314 has a line length LL that is at least as wide as the width Wd of wafer 70 (e.g., a length of L≧200 mm for a 200 mm diameter wafer). The line image 314 also has a line width WL. It is desirable to have the line width WL such that the laser annealing is accomplished in approximately 1 millisecond (ms). If the platen 60 is moving at 60 RPM, and if the platen holds twenty 200-mm wafers, then, the wafers are moving at roughly 4000 mm/sec. A laser beam width of WL=4 mm would produce an annealing time of 1 ms. In an example, the line length LL and the line width WL of line image 134 at wafer surface 72 is defined by beam-conditioning optical system 316. The position of the mirror 320 can be adjusted so that laser beam 312 is incident upon wafer surface 72 at a select angle (e.g., normal incidence, the Brewster angle, etc.).
An example laser annealing process performed using system 10 generates a peak temperature TS at the wafer surface 72 of between 600° C. and 1000° C. If the temperature of platen 60 is at 200° C., then laser beam 312 needs to raise the surface temperature TS of wafer 70 by 400° C. to 800° C.
It is also desirable to use a wavelength λ for laser beam 312 such that the laser beam radiation is absorbed within the thermal diffusion length of the laser anneal. For a 1 ms anneal, and a silicon wafer 70, the thermal diffusion length is roughly 100 microns. Hence, it is desirable that the absorption length be <100 microns. For a silicon wafer, this implies that the laser wavelength λ be less than approximately 1 micron.
It is desirable to have an annealing time of approximately 1 ms at each point on the wafer 70 (i.e., a “dwell time”) because it has been shown that high temperature annealing for short durations produces elastic deformations rather than plastic deformations. This way, the thin ALD film 74 and the silicon wafer expand elastically. This requirement, along with the peak temperature requirement, is sufficient to adequately design laser annealing system 300.
It is noted that in the four-chamber-section embodiment of chamber 20, one or both of chamber sections 41A and 41C can be a laser-annealing process chambers while chamber sections 41B and 41D can be non-processing chambers. Any combination of processing and non-processing chambers consistent with carrying out a viable ALD process can be used in system 10.
Multichamber ALD System with Plasma Processing
The plasma 410 includes plasma species (e.g., charged ions, such as oxygen radicals O*) that chemically react with wafer surface 72 or film layer 74L that resides on the wafer surface. The plasma 410 moves towards wafer surface 72 due to the pressure differential between the plasma source system 400 and the wafer surface. In an example, plasma source system 400 can be operably arranged relative to more than one chamber section 41. Thus, in an example, system 10 can be used to perform plasma-enhanced ALD (PE-ALD) in at least one of chamber sections 41. In another example, plasma 410 can be used to clean wafers 70 between processing steps, e.g., by providing plasma source system 400 in operable arrangement with respect to a purge or non-process chamber section 41.
Throughput Considerations
The systems and methods disclosed herein are designed to provide relatively high throughput of processed wafers. An example of a high throughput is 10 or more 6-inch wafers per hour having deposited thereon 0.25 micron ore more of material.
Consider now example process of forming GaN using system 10 and the corresponding methods as described above using the basic process set forth in Table 2. A GaN crystal lattice has a dimension of 0.3 nm. At a 60 RPM rotation rate for platen 60, there are 3600 cycles (i.e., full rotations) per hour, with each cycle depositing one ALD film layer 74L, so that we can grow an ALD film 74 with a thickness THF of about 1 micron of GaN in one hour. The process chamber size (e.g., platen radius R) determines the number of wafers 70 that can fit on the platen 60, but the platen radius R can be made large enough to accommodate more than 20 six-inch wafers on a single platen. This is twice as many wafers and four times the film thickness of the example high-throughput process mentioned above, i.e., represents about an 8× throughput improvement.
It will be apparent to those skilled in the art that various modifications to the preferred embodiments of the disclosure as described herein can be made without departing from the spirit or scope of the disclosure as defined in the appended claims. Thus, the disclosure covers the modifications and variations provided they come within the scope of the appended claims and the equivalents thereto.
Number | Date | Country | |
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62233575 | Sep 2015 | US |