1. Field of the Invention
Embodiments of the present invention relate to the deposition of materials on multiple substrates, and more particularly to, an apparatus useful for chemical vapor deposition and atomic layer deposition during the fabrication of semiconductor devices.
2. Description of the Related Art
The fabrication of semiconductor devices involves the sequential deposition of various materials onto a substrate. Deposition may be accomplished through chemical vapor deposition (CVD), atomic layer deposition (ALD), or other methods. Such deposition steps take place in one or, more commonly, a series of process chambers. For example, the deposition of silicon may be accomplished by placing a substrate in a process chamber, heating the substrate to a desired temperature, and then introducing silane or a similar precursor such as disilane, dichlorosilane, silicon tetrachloride and the like, with or without other gases, into the process chamber. The precursor disassociates at the hot substrate surfaces resulting in silicon deposition.
It is desirable to increase throughput by adjusting operating parameters within the process chamber. Such parameters include pressure, temperature, deposition gas injection rate, purge gas volume, and so forth. At the same time, it is important to maintain quality of the layers in the fabricated semiconductor devices, such as providing uniform film thickness. Optimum quality control may be obtained by using a single wafer processing reactor, which includes a process chamber that performs one or more process steps on a single substrate. However, single wafer processing has limited throughput.
A parallel wafer processing reactor has been used to increase throughput. A parallel wafer processing reactor places a plurality of substrates into a vertical stack within the same reactor. Examples of a parallel wafer processing reactor are described in U.S. Pat. No. 6,352,593, U.S. Pat. No. 6,352,594, U.S. patent application Ser. No. 10/216,079, and U.S. patent application Ser. No. 10/342,151, all of which are incorporated by reference herein.
The parallel wafer processing reactor described in the above patents and patent applications allows for the deposition of silicon (or other material) simultaneously on multiple substrates arranged in parallel orientation to one another. It employs a multi-plenum temperature-controlled vertical injector to provide uniform gas flow across the wafer, and provides an isothermal wafer environment that results in good wafer temperature uniformity. These two features enable the deposition of a variety of films at relatively high deposition rates over a wide process space. As a consequence, it provides the process benefits of single wafer processing reactors (i.e., uniform, high quality films, large process windows, low cycle times, multi-step sequential processing, vacuum integrated processing and flexible lot sizes), while processing numerous substrates at a time to increase throughput.
Embodiments of the present invention provide a substrate carrier for a parallel wafer processing reactor that further increases process throughput. In one embodiment, the substrate carrier includes a plurality of susceptors arranged horizontally in a vertical stack. The substrates are mounted between pairs of susceptors on two or more supports provided around the outer periphery of the susceptors. The number of substrates mounted between each pair of susceptors may be the same or different but is two or more between at least one pair of susceptors.
Embodiments of the present invention also provide a parallel wafer processing reactor for processing substrates. The reactor includes a process chamber and a substrate carrier having a plurality of horizontally arranged susceptors and a support, disposed between at least one pair of said susceptors, for holding at least two substrates.
In one embodiment of the present invention, the support between each pair of susceptors includes two opposing spacers. Opposite ends of the wafers are supported on these shoulders. In another embodiment of the present invention, the support between each pair of susceptors includes three spacers arranged so that first, second and third ends of the wafers are supported on these shoulders. The first, second and third ends of the wafers have radial positions on the wafer that are 120° from each other.
The substrate carrier according to embodiments of the present invention offers certain advantages over the prior art substrate carrier designs. They include an increase in capacity for substrates within a given isothermal zone, and a reduction in cost by decreasing the number of susceptors.
So that the manner in which the above recited features of the present invention can be understood in detail, a more particular description of the invention, briefly summarized above, may be had by reference to embodiments, some of which are illustrated in the appended drawings. It is to be noted, however, that the appended drawings illustrate only typical embodiments of this invention and are therefore not to be considered limiting of its scope, for the invention may admit to other equally effective embodiments.
The susceptors 407 are made up a generally planar platen 417 and two or more discrete post members 419 disposed radially around the platen. The platen portion 417 is designed to be heated, such as by means of a heating element (not shown). To accommodate heating of the platen 417, the susceptors 407 are preferably made from a refractory, high thermal conductivity material such as SiC coated graphite, SiC coated SiC or solid SiC. A variety of other materials may also be used, although various combinations of SiC and graphite appear to be optimal for high temperature applications. Preferably, the susceptors 407 have a larger diameter than the substrates 404. For some processes such as thermal annealing or oxidation, the susceptor diameter is equivalent to the substrate diameter.
The susceptors 407 play several important roles. The susceptors 407 pre-heat the process gases and induce a stable flow and stable thermal boundary layer before the gas flows reach the substrates 404, minimizing wafer edge effects. The thermal mass of the susceptors 407 also exceeds the thermal mass of the substrates 404. The susceptors 407 also help control the gas flow through the substrate carrier 406, reducing the need for dummy wafers. They also reduce the formation of flow eddies or zones of gas recirculation that may exacerbate gas phase formation of particles.
The susceptors 407 are vertically stacked so that the respective platens 417 are generally parallel to one another.
The geometrical variables associated with the susceptors 407 that influence process performance are: (a) clearance above and below each wafer, (b) the inter-susceptor spacing, and (c) the susceptor diameter. The optimal clearances above and below the substrate 404 are somewhat process dependent. Typically, equal clearances above and below the wafer result in the same film thickness and film properties on both sides of the wafer. This is generally desirable since wafers retain their flatness following deposition. The films on the backside of the wafer may be stripped at some point in the process flow. The distribution of gases above and below each wafer depends primarily on the clearances above and below the wafer. As the clearances are increased, a larger fraction of the process gases introduced through the gas injection manifold 200 (see
For in situ doped Si films, the optimal clearance between the substrate 404 and the adjacent susceptor 407 is in the range of 0.15 inches to 0.30 inches to ensure that a proper amount of process gases flow across the substrates 404 rather than around the substrates 404. The substrates 404 may be placed away from the mid-plane of the gaps 408 to alter the ratio of gas flow over the substrates 404 to the gas flow under the respective substrates 404. The gaps 408 retain their isothermal near black body characteristics for intersusceptor spacings in the range of 0.25 inches to 1.25 inches for susceptors that are 13.6 inches in diameter (i.e. preferred minimum aspect ratio of the resulting gap 408 between susceptors is greater than 10:1).
It is desirable to increase the load size of the substrate carrier 406 without compromising the deposition rates, film uniformities, and film properties. Increasing load size is accomplished herein by placing more than one substrate 404 between each pair of susceptors 407. The clearances above and below each substrate 404 are selected to meet the desired process parameters as set forth above. By placing two, three, four or more substrates 404 instead of only one substrate 404 between adjacent susceptors 407, the load size can be increased without making other major changes to the reactor 10.
are used between two adjacent susceptors 407, the three spacers 402 support first, second and third ends of the substrates 404 that equidistant (120°) from one another.
Optionally, objects serving as insulators or thermal conductors may be selectively placed between certain adjacent susceptors 407. Insulators would be of particular value when placed between susceptors 407 at the extremities of the substrate carrier 406 in order to reduce the heat loss from the top and bottom of the substrate carrier 406. A bottom and/or top heater can also optionally augment the heat flux to the bottom and/or top of the substrate carrier 406.
In a case where three substrates 404 are disposed between pair of susceptors 407, the substrates 404 closest to either susceptor 407 may heat up more quickly than the substrate 404 that is sandwiched between the two outer substrates 404. An embodiment of the invention illustrated in
The process results for the substrate carrier 406 with four wafers per susceptor pair (50 wafers in total) are shown in
For many CVD and ALD processes, it is necessary to precisely control the temperature of the chamber walls. In many cases, the ideal temperature is an intermediate temperature between the process temperature and the room temperature. At the ideal temperature, there should be no condensation of precursors or reaction by-products, and films (if deposited) must be contiguous, low stress and not powder-like. These requirements are usually met at temperatures approaching the process temperature. Since the deposition rate generally falls off at lower temperatures, it is preferable to control the wall temperature to a value slightly below the process temperature so that the rate of build-up on the chamber walls is decreased. Eventually, the build-up on the chamber walls will be thick enough requiring a chamber clean. Since it is infeasible to remove the chamber for cleaning and in situ chamber cleaning may not remove the entire deposited film, one or more removable liners that cover the chamber wall may be used. The liners can be made from a variety of materials including SiC, SiC on SiC, SiC on graphite, anodized aluminum or composite structures comprising a refractory material and an insulating material such as SiO2, AIN, polymers, etc.
For liner surface temperatures above 300° C., the preferred material and method of construction is SiC, SiC on SiC, SiC on graphite that is closely spaced (0.25 mm-0.75 mm) away from a chamber wall maintained at a lower temperature. By controlling the gap between the liner and the chamber wall, the temperature of the liner and the outer skin of the chamber wall can be adequately controlled. This small gap provides thermal isolation, but is generally not large enough for the precursor or reaction by-products to accumulate in this cavity. For lower liner temperatures, the liner can be placed in contact with the chamber wall with an intervening insulator.
The liner has advantageous utility in both in situ cleaning and ex situ cleaning. For in situ cleaning, the liner may be cleaned through known steps for etching/removal of deposited films. For ex situ cleaning, the liner may be removed and cleaned or replaced, avoiding extensive cleaning of other chamber hardware.
For some applications, a fixed volume delivery scheme may be necessary for more than one precursor. Since the fixed volume should be located in close proximity to the point of injection, space constraints limit the number of fixed volumes that can be mounted adjacent to an injector. In such cases, using multiple spatially separated injectors simplifies the integration task. Multiple, spatially separated injectors offer the following benefits:
The fixed volume delivery mechanism, illustrated in
The flow to the fixed volume 510 can optionally be metered using a flow monitor or flow controller 525 such as a low pressure mass flow controller (for vapor draw) or a mass flow monitor (for bubbler mode). The mass flow monitor 525 measures the flow rate of precursor in the carrier stream and may optionally adjust the carrier flow or bubbler operating conditions to maintain a constant flow rate of precursor. In an actual implementation, additional fixed volume states denoting when the fixed volume 510 is idle, isolated or sealed, filled, topped or pumped may be used during operation.
The parallel wafer processing reactor 10 described herein also enables epitaxial and selective epitaxial deposition of semiconductor films. Low temperature epitaxial and selective epitaxial deposition of silicon and silicon germanium films is becoming increasingly important for next generation semiconductor devices. The parallel wafer processing reactor 10 described herein can be extended to accomplish the deposition of such films. The parallel wafer processing reactor 10 is suitable for epi processing because it possesses several of the essential attributes for epi processing such as uniform distribution of dopants across the wafer and across the entire wafer load, ability to deliver radicals, and suppression of oxide re-growth. The attributes of the parallel wafer processing reactor 10 that enable epitaxial processing are listed below:
In situ chamber cleaning which involves the etching/removal of deposited films from the reactor surfaces is widely used in single wafer processing reactors. The alternative cleaning methodology is ex situ cleaning in which the process chamber is opened, parts with deposited film are swapped with clean parts, and the chamber is physically wiped down. Ex situ cleaning by its very nature is time consuming because it involves venting of the chamber to atmosphere, replacement of components, and an extended chamber qualification/conditioning before processing of wafers can begin. For thermal systems, the overhead associated with cool-down of the system prior to venting and heat-up of the system following the ex situ clean add to the overall down-time. If the chamber has been exposed to toxic gases during wafer processing, gas specific abatement procedures may have to be performed before the reactor can be opened for servicing. For these reasons, in situ chamber cleaning is advantageous over ex situ chamber cleaning.
In one approach for in situ cleaning, the boat is allowed to cool-down in the upper chamber while etching gases are introduced in the process chamber to etch the films off the thermal diffusion shields and the liners (if installed). Once the films have been etched off the shields and the liners, the boat is re-introduced into the process chamber and the boat can be cleaned in situ or processing can resume. In this type of reactor, the deposition on the thermal diffusion shields exceeds the deposition on the boat by a factor of 1.5×-3× depending on the process conditions and the temperature differential between the thermal diffusion shields and the boat. Thus the boat is not cleaned as frequently as the thermal diffusion shields.
In a hybrid in situ cleaning approach, illustrated in
A variety of etching gases have been used for in situ cleaning including NF3, atomic fluorine, F2, chlorofluorocarbons, CIF3, HF, HCI, etc. These gases are suitable for use in the parallel wafer processing reactor 10 described herein except that the etch rate, surface temperatures, and compatibility with reactor materials must be considered. Very low etch rates are generally unacceptable since they translate to very long in situ clean times that effectively degrade system uptime in a production environment. Many fluorinated and chlorinated gases attack metallic surfaces, polymeric materials and coatings (e.g. SiC, AIN) above a certain threshold temperature. Attack not only causes corrosion, but low volatility metal fluorides/chlorides can remain resident in the reactor and contaminate the film during subsequent processing. Typically surfaces temperatures should be below 300° C. to avoid attack of metallic surfaces and SiC. Quartz components are relatively immune to attack and can sustain substantially higher temperatures without being etched appreciably.
Atomic fluorine can be generated via a variety of methods. A conventional approach is to flow a fluorine containing gas through a plasma source. Alternatively, the fluorine containing gas can be introduced into the plasma plume downstream of the plasma source where the ions, excited atoms/molecules, and radicals formed in the plasma source dissociate the fluorine containing gases to generate atomic fluorine. The plasma source can be designed so that the plasma plume is intentionally very long. Introducing reactants downstream of the plasma source may result in more efficient dissociation into species that are effective in etching. For example in the case of CF4, complete dissociation into CF and F atoms may be less effective at etching SiO2 compared to a partial dissociation into CF2 and F. Adding the cleaning gas to the plasma source may also damage the source via etching of the plasma containing tube. In either case, the plasma source may be pulsed to enhance the atomic fluorine generation rate. Pulsing the plasma source allows high power levels to be used for short periods of time without overheating the plasma source. Plasma pulsing is also a means to control the types of radicals formed. Instead of using a plasma source, atomic fluorine can also be generated by thermally cracking a fluorine containing gas using a hot filament.
A small footprint, high throughput wafer handler for the parallel wafer processing reactor 10 is illustrated schematically in
In the architecture shown in
The process chamber 850 remains idle from the point when the first set of wafers has exited the process chamber 850, and the next set of wafers is loaded into the process chamber 850. Thus the cycle time for a set of wafers to be processed is the sum of the processing time and the total wafer handling time. For short processes, the total wafer handling time may exceed the process time which limits the maximum throughput available.
While the foregoing is directed to embodiments of the present invention, other and further embodiments of the invention may be devised without departing from the basic scope thereof, and the scope thereof is determined by the claims that follow.
This application is a continuation-in-part of U.S. application Ser. No. 10/216,079, filed Aug. 9, 2002, which is a continuation-in-part of: (a) U.S. application Ser. No. 09/954,705, filed Sep. 10, 2001, now U.S. Pat. No. 6,780,464, which is a continuation-in-part of U.S. application Ser. No. 09/396,588, filed Sep. 15, 1999, now U.S. Pat. No. 6,287,635 (which claims the benefit of U.S. Provisional Application Ser. No. 60/100,594, filed Sep. 16, 1998), which is a continuation-in-part of: (i) U.S. application Ser. No. 08/909,461, filed Aug. 11, 1997, now U.S. Pat. No. 6,352,593, (ii) U.S. application Ser. No. 09/228,835, filed Jan. 12, 1999, now U.S. Pat. No. 6,167,837 (which claims the benefit of U.S. Provisional Application Ser. No. 60/071,572, filed Jan. 15, 1998), and (iii) U.S. application Ser. No. 09/228,840, filed Jan. 12, 1999, now U.S. Pat. No. 6,321,680 (which claims the benefit of U.S. Provisional Application Ser. No. 60/071,571, filed Jan. 15, 1998); and (b) U.S. application Ser. No. 09/396,590, filed Sep. 15, 1999, now U.S. Pat. No. 6,506,691 (which claims the benefit of U.S. Provisional Application Ser. No. 60/100,596, filed Sep. 16, 1998).
Number | Date | Country | |
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60100594 | Sep 1998 | US | |
60071572 | Jan 1998 | US | |
60071571 | Jan 1998 | US | |
60100596 | Sep 1998 | US |
Number | Date | Country | |
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Parent | 10216079 | Aug 2002 | US |
Child | 10966245 | Oct 2004 | US |
Parent | 09954705 | Sep 2001 | US |
Child | 10216079 | Aug 2002 | US |
Parent | 09396588 | Sep 1999 | US |
Child | 09954705 | Sep 2001 | US |
Parent | 08909461 | Aug 1997 | US |
Child | 10216079 | US | |
Parent | 09228835 | Jan 1999 | US |
Child | 10216079 | US | |
Parent | 09228840 | Jan 1999 | US |
Child | 10216079 | US | |
Parent | 09396590 | Sep 1999 | US |
Child | 10216079 | US |