10 casing
11 bottom surface
20 electrode
30 hole
60 exhaust chamber
110 casing
300 hole
320 insulating film
120 bottom plate
410 susceptor
420 semiconductor substrate
A minute gap
The best mode for carrying out the present invention will be described. Embodiments will be described in a particular manner in order to facilitate the understanding of the inventive concept, and hence it is not to be understood that the present invention is limited to the following embodiments.
An outer surface 20a, an inner surface 20b and a side surface 20c of this electrode 20 are covered with an insulating film 22 composed of Al2O3 having a thickness of 150 μm. In addition, the electrode 20 is formed so that cooling water is supplied therein for circulation and reaches the portion forming the hole 30 at the front end, that is, is formed so as to cool the hole 30 of the electrode 20.
A central conductor 40 is provided along the central axis of the casing 10 and is located at the center of the hole 30, and a front end surface 41 of the central conductor 40 is disposed at the same height (the same x axis coordinate) as that of the outer surface 20a of the electrode 20. In addition, an outer surface of a front end portion of the central conductor 40 is covered with an insulating film 42 of Al2O3 having a thickness of 150 μm. In this configuration, a minute gap A is formed between a circular contour 23 of a front end portion which forms the hole 30 of the electrode 20 and a circular contour 43 of the front end surface 41 (bottom surface) of the central conductor 40. The width of the minute gap A is in the range of 0.1 to 0.2 mm. In the space inside this central conductor 40 including a front end of the space, cooling water is circulated so as to cool the front end portion and the front end surface 41 of the central conductor 40.
In addition, on the casing 10, a waveguide 50 for guiding a microwave into the casing 10 is provided, and the microwave guided by this waveguide 50 is converted from a waveguide mode to a coaxial mode by a mode converter 52 and is then transmitted to the minute gap A side. The casing 10 and the electrode 20 are both grounded. The microwave supplied by the structure as described above is concentrated at the minute gap A, and as a result, the electric field density at the minute gap A is maximized.
In the side surface of the casing 10, a gas inlet 12 is provided, and from this gas inlet 12, a gas for generating plasma is supplied. In this example, a He gas was used. In the other side surface of the casing 10, a gas induction port 13 is provided, and from this gas induction port 13, a fluorocarbon gas is introduced. In this example, a CF4 gas was used.
Under the electrode 20, an exhaust chamber 60 is provided and is formed so that gases flowing through the gas inlets 12 and 13 are made to pass through the minute gap A by evacuation from an exhaust hole 61. In addition, a transport device 62, which collects generated particles and transports them outside the exhaust chamber 60, is provided in the exhaust chamber 60 and under the minute gap A. The transport device 62 is formed so that particles are transported in the direction perpendicular to the plane of
The apparatus described above was operated as described below. Cooling water was circulated inside the central conductor 40 and inside the electrode 20. Next, from the waveguide 50, a microwave was supplied having a frequency of 2.45 GHz, a peak electric power of 300 W, a pulse repetition frequency of 10 kHz, and a duty ratio of 50%. The pressure inside the casing 10 was 1 atom, and the exhaust amount from the exhaust port 61 was controlled so as to introduce a He gas at a flow rate of 2 L/min into the casing 10 from the gas inlet port 12. Under the conditions described above, He plasma was stably generated at the minute gap A. Next, the exhaust amount from the exhaust port 61 was controlled so as to introduce a CF4 gas at a flow rate of 2 L/min into the casing 10 from the inlet port 13. As a result, at the minute gap A, by decomposition of CF4 and polymerization reaction, particles of polytetrafluoroethylene were generated, then fell on the transport device 62, and were accumulated. In this step, the generation of carbon dioxide was not observed. The decomposition rate of CF4 was 80% or more.
Next, by using the above apparatus, an Ar gas and a N2 gas were used instead of a He gas. Since a He gas is expensive, when an Ar gas and a N2 gas can be used, significant industrial advantages can be obtained. Hence, first of all, by using an apparatus in which the insulating film 22 and the insulating film 42 are not formed on the metal electrode 20 and the central conductor 40, respectively, experiments were each carried out by continuous supply of a microwave having an electric power of 200 W. However, the electrode 20 and the central conductor 40 were cooled by circulating cooling water, and the pressure was set to atmospheric pressure. Three experiments, that is, an experiment in which a He gas was supplied at a flow rate of 2 L/min, an experiment in which an Ar gas was supplied at a flow rate of 2 L/min, and an experiment in which a N2 gas was supplied at a flow rate of 2 L/min, were carried out. As a result, in the case of a He gas, the generation of stable plasma was observed, and on the other hand, in the cases of an Ar gas and a N2 gas, it was difficult to uniformly generate stable plasma at the ring-shaped minute gap A.
Next, an apparatus was used in which the insulating film 22 was formed on the side surface, the outer surface, and the inner surface of the metal electrode 20, and the insulating film 42 was formed on the surface of the front end portion of the central conductor 40. Next, as described above, three types of gases were separately supplied at a flow rate of 2 L/min. By the three types of gases, stable plasma was observed at the ring-shaped minute gap A. In order to investigate the plasma state, a gas temperature was measured by an ICCD camera and an electrode temperature was measured by FTIR. The emission spectrum was measured by an ICCD camera, and the gas temperature of plasma was obtained from the second positive band emission. That is, the coefficient was determined so that the simulation spectrum coincides with the measured spectrum, and the rotation temperature was obtained. This rotation temperature was regarded as the plasma temperature. In the following results, the values obtained for the rotation temperature are all shown as the plasma temperature. The results are shown in
In addition, after the insulating film 42 was not formed on the surface of the central conductor 40, and the insulating film 22 was only formed on the electrode 20 as described above, an experiment similar to that described above was performed. In this case, the results approximately similar to those described above were obtained although the stability was slightly inferior. In addition, after the insulating film 42 was formed on the surface of the central conductor 40, and the insulating film 22 was not formed on the electrode 20, an experiment similar to that described above was performed. In this case, relatively stable plasma was also observed although the stability was more degraded than that described above. Accordingly, it is most preferable that the insulating films be provided for both the central conductor 40 and the electrode 20.
Next, the plasma temperature with time from the application of microwave was measured in a manner similar to that in Example 2. The results are shown in
Next, by using a microwave having a frequency of 2.45 GHz, an average electric power of 200 W, and a pulse period of 100 kHz, the plasma temperature of each gas was measured with the change of the duty ratio. The other conditions were the same as those in Example 2. The measurement results are shown in
Next, in Example 4, in the case in which the duty ratio was set to 100% (continuous electricity supply) and cooling was not performed for the electrode 20 and the central conductor 40, the plasma temperature was measured by introducing a N2 gas. As shown in
According to Example 4, it is understood that water cooling of the central conductor 40 and the electrode 20 is effective for the control of the plasma temperature; hence, for further investigation, the relationship between the plasma temperature and the temperatures (when the temperatures of the two described below are not necessarily discriminated from each other, the temperatures are simply referred to as “electrode temperature”) of the central conductor 40 and the electrode 20 (when the above two are not necessarily discriminated from each other, they are simply referred to as “electrode”) was measured. However, in this experiment, gases were not made to flow and were enclosed in a closed space. That is, the experiment was performed while the exhaust chamber 60 shown in
The plasma generation apparatus can be designed to have the structure shown in
In this step, by the electric power of the microwave, He plasma is generated at the minute gap A portion, NF3 and H2O are decomposed, and F radicals, H radicals, OH radicals, F ions, F2 molecules, HF molecules, and the like are generated. By the radicals and the like, a semiconductor substrate placed on a rotary susceptor 410 provided under the hole 300 is etched. The plasma thus generated is observed by an absorption spectroscopy using laser and is controlled to be placed in a most preferable state.
As is the case of the above examples, for example, the microwave may be a continuous wave or a pulse wave, and in the case of a pulse wave, the plasma temperature can be controlled by the cycle period and the duty ratio of the pulse.
The present invention provides an apparatus stably generating plasma. In particular, the apparatus can be advantageously used at atmospheric pressure. In semiconductor etching, film-forming process, machining, cleaning, surface reforming, and the like, which use plasma, it is not necessary to evacuate a process chamber, and hence this apparatus is particularly advantageous. Since the electron density of atmospheric plasma is approximately 1015/cm3, which is approximately 3 orders of magnitude larger than that of low-pressure high density plasma, high-density radicals and ions can be generated, and hence a high rate process can be performed. In addition, since gases can be decomposed and polymerized by plasma, the recovery of exhaust gas in the form of particles and the formation of a fluorocarbon gas and radicals thereof from graphite and a F2 gas can be advantageously performed.
According to the present invention, plasma effectively used for semiconductor processes and the like can be stably supplied. Hence, in a semiconductor device manufacturing plant, this technique is significantly effective.
As has thus been described, since individual constituent elements can be separated and extracted, when extracted constituent elements are independently used in combination, one aspect of the invention may be formed. When an optional constituent element disclosed in Claims is eliminated, one aspect of the present invention may also be formed.
Number | Date | Country | Kind |
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2004-40628 | Feb 2004 | JP | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/JP05/01003 | 1/26/2005 | WO | 00 | 7/9/2007 |