The present invention relates to the use of fluorine gas to perform chamber cleaning in a production process for flat panel displays (FPD) and photo voltaic (PV) thin films.
In the production of FPD and PV thin films, frequent cleaning of the deposition chambers is required. This cleaning step reduces the time available for production and therefore increases overall production costs.
A significant problem for the cleaning step relates to the speed at which the source gas can be introduced to the Remote Plasma System (RPS) for production of fluorine radicals that can be introduced to the chamber. Some fluorine source gases will extinguish the fluorine plasma in the RPS if introduced too rapidly.
A common source gas for fluorine radical production is nitrogen trifluoride (NF3). However, NF3 exhibits the problem noted above, that the plasma is extinguished if its introduction to the RPS is too rapid or ramped up at too great a speed. U.S. Pat. No. 6,374,831 addresses this issue and establishes a limit of 1.67 scc/sec2 as the maximum rate that NF3 flow can be increased to avoid extinguishing the RPS. This means that in a practical setting the NF3 flow can be stepped up from zero in increments of about 100 sccm every second until the full desired flow is achieved. One standard type of RPS is the Astron EX RPS that has a maximum flow of 6,000 sccm. Therefore, when using such an RPS and NF3, the flow must be ramped up over a 60 second period. In addition, during ramp up, the cleaning rate is at less than the maximum.
U.S. Pat. No. 6,880,561 suggests the use of F2 as the source gas, but does not use an RPS. Rather, in this patent, the chamber must be heated to greater than 450° C. for cleaning to take place. This also adds time to the process and the additional cost of a heating system.
There remains a need in the art for improvements to chamber cleaning for FPD and PV thin film manufacturing.
The present invention overcomes the problems noted above and provides for more rapid chamber cleaning. In particular, the present invention uses a F2 source gas along with a standard RPS, such as an Astron EX RPS, to produce fluorine radicals to perform chamber cleaning.
The present invention provides a system and method for performing chamber cleaning more rapidly than has been done in the prior art. In particular, the present invention uses F2 as the source gas for an RPS to form fluorine radicals used in the chamber cleaning operation.
By using F2 the disadvantage of the prior art noted above can be overcome. In particular, no ramping up of the F2 flow is required. Rather, the F2 can be introduced to the RPS at any flow from 15% to 100%, preferably 80% to 100%, of the maximum allowed by the RPS. This means that cleaning the time to perform chamber cleaning can be significantly reduced.
The present invention will be further described with reference to
The present invention provides several advantages over the prior art. In particular, the chamber cleaning time can be significantly reduced. In one test case, when using F2 in accordance with the present invention, the chamber cleaning step was completed in 50 seconds, or roughly the time it would take to simply ramp up to full operation when using NF3. By using F2 at a higher flow rate from the outset, the cleaning can proceed at a faster rate from the beginning of the cleaning cycle and ramping up of the F2 flow is not required. Rather, the F2 can be introduced to the RPS at any flow from 15% to 100%, preferably 80% to 100% of the maximum allowed by the RPS.
Using the full flow of the cleaning gas at the start of the cleaning step produces a significant burst of fluorine radicals at the beginning of the cleaning cycle, resulting in a higher cleaning rate at the beginning of the cleaning cycle when the maximum amount of deposit to be cleaned is present. In addition, the presence of high radical concentration and maximum deposit to be cleaned results in an exothermic reaction that heats the deposits and increases cleaning speed. No separate heating system for the chamber is required.
The present invention also allows for optimization of the cleaning cycle. For example, the cleaning cycle can start with a very high flow and pressure for rapid material removal. However, such rapid cleaning normally exhibits poor uniformity that does not reach the corners. Then pressure can be reduced to improve uniformity. This works very well, because the corners have thinner deposits at the start of the cleaning process and therefore can be effectively cleaned after the bulk of the deposit is rapidly removed. For example, the F2 may be introduced at a high pressure of 1-100 torr, preferably 1-50 torr at the beginning of the cleaning cycle and then reduced to 0.1 to 1 torr near the end of the cleaning cycle.
By using the present invention wherein argon starts the plasma followed immediately by a high flow of F2 (with argon turned off), the cleaning rate can be greatly increased. This means that the time to perform chamber cleaning can be significantly reduced. Further, by providing a higher flow at the outset, the cleaning can proceed at a full rate from the beginning of the cleaning cycle. The present invention allows for use of standard existing RPS and chamber equipment without any required changes to configuration or operating parameters.
The present invention provides several advantages over the prior art. In particular, no dilution of the cleaning gas is necessary and no ramp up of the cleaning gas flow rate is required. Further, by immediately providing a high flow of the cleaning gas, the initial cleaning rate is higher and the surface being cleaned is heated to even further increase cleaning speed.
The present invention is particularly useful for cleaning chambers used in the production of flat panel and solar PV devices because of their size. However, the present invention is useful for any chamber cleaning application in the semiconductor manufacturing industry. The present invention is useful for cleaning deposits of nearly any type commonly encountered in semiconductor manufacturing, including Si, W, Ti, SiN, SiO2, etc.
It will be understood that the embodiments described herein are merely exemplary, and that one skilled in the art may make variations and modifications without departing from the spirit and scope of the invention. All such variations and modifications are intended to be included within the scope of the invention as described hereinabove. Further, all embodiments disclosed are not necessarily in the alternative, as various embodiments of the invention may be combined to provide the desired result.
This application claims priority from International Application No. PCT/US2009/034500 filed Feb. 19, 2009 claiming priority from U.S. Application No. 61/030,347 filed Feb. 21, 2008.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/US2009/034500 | 2/19/2009 | WO | 00 | 10/29/2010 |
Number | Date | Country | |
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61030347 | Feb 2008 | US |