The present invention relates to a method and apparatus for fabricating semiconductor devices such as various transistors and integrated circuits.
In recent years, methods and apparatus which use lasers to manufacture semiconductor devices have been developed. Examples of these methods and apparatus include laser etching, or laser scribing, in which films are etched and patterned, laser annealing in which the crystalline state of films or their surfaces are changed by laser irradiation, and laser doping in which an impurity is diffused into films or their surfaces by laser irradiation within an ambient containing the impurity.
In these conventional semiconductor fabrication methods using lasers, a substrate already processed by other film formation apparatus or etching apparatus is first placed in position inside a laser processing apparatus. The inside of this apparatus is evacuated and the substrate is heated and then the substrate is processed by laser radiation. Consequently, the productivity is very low.
It is an object of the present invention to provide a method of fabricating semiconductor devices with improved productivity.
It is another object of the invention to provide an apparatus capable of fabricating semiconductor devices with improved productivity.
An apparatus according to the present invention comprises a multi-chamber system consisting of a film formation apparatus (e.g., a plasma CVD apparatus, a sputtering apparatus, a thermal CVD apparatus, or a vacuum evaporation apparatus), an etching apparatus, a doping apparatus (e.g., a plasma doping apparatus or an ion implanter), a thermal processing apparatus (e.g., a thermal diffusion apparatus or a thermal crystallization apparatus), a vacuum apparatus such as a preliminary chamber, and a laser processing apparatus (e.g., a laser etching apparatus, a laser annealing apparatus, or a laser doping apparatus). The novel apparatus performs processing without exposing each substrate to the atmosphere at all. In this system, the evacuation can be effected in a greatly shortened time. In addition, when the substrate is transported, it is protected from contamination.
Also, various annealing methods making use of infrared light irradiation rather than laser irradiation are available. For example, an amorphous silicon film formed on a glass substrate is crystallized by heating and then irradiated with infrared radiation. As a result, the crystallinity can be enhanced further. Infrared radiation is absorbed more readily by the thin silicon film than by the glass substrate. Only the thin silicon film can be heated without heating the glass substrate very much. This is advantageous. Furthermore, it is considered that the obtained effect is comparable to the effect produced by a thermal anneal conducted above 1000° C.
An anneal using such irradiation of infrared radiation can be completed within several minutes. Therefore, this is known as a rapid thermal anneal (RTA). This anneal can be advantageously conducted after an insulating film is formed on a semiconductor layer. In this case, the level in the interface between the semiconductor layer and the insulating film can be reduced, so that the interface characteristics can be enhanced. For example, after an active layer (in which a channel formation layer is formed) for an insulated-gate field-effect transistor is formed, a silicon oxide film becoming a gate-insulating film is formed. Subsequently, a rapid thermal anneal process is carried out. In this way, the characteristics at and around the interface between the channel and the gate-insulating film which are an important factor for the insulated-gate field-effect transistor can be improved.
Other objects and features of the invention will appear in the course of the description thereof, which follows.
FIGS. 5(A)-5(F) are cross-sectional views illustrating a series of operations successively performed to fabricate semiconductor devices according to the invention; and
Referring to
The chamber 1 is further equipped with electrodes 4 and 5. A substrate or sample 6 to be processed is placed on the electrode 5. An RF power supply 3 of frequency, for example, of 13.56 MHz is connected with the electrode 4. An adequate gas such as monosilane or disilane is admitted into the chamber to induce electric discharge between the electrodes. In this way, a film is formed on the substrate 6. If necessary, the substrate may be heated. Where monosilane is used as the above-described gas and the substrate is maintained below 300° C., an amorphous silicon film is formed on the substrate.
Since such amorphous silicon film does not have excellent electrical characteristics, the silicon is crystallized by laser annealing to improve the characteristics. The chamber 2 is provided with a window 14. Laser light emitted from a laser 11 passes through the window 14 via a mirror 12 and a lens 13 and impinges on a substrate 17 that is placed on a sample holder 15. The substrate 17 is heated to 300-500° C., preferably 300-400° C., by a heater 16. This heating operation is indispensable to the process where crystallization is effected with high reproducibility.
The sample holder 15 is capable of moving gradually to the right as viewed in the figure while carrying the substrate 17. As a result, the whole surface of the substrate can be processed by the laser light. Let us assume that the substrate measures 300 mm by 400 mm. The whole surface of the substrate can be treated with the laser light by shaping the cross section of the laser beam into a rectangular form measuring 2 mm×350 mm. If the holder moves at a speed of 20 mm/sec, the time taken to process one substrate is 400/20=20 seconds.
A substrate on which an amorphous silicon film is formed by the plasma CVD apparatus 1 is transported into the laser processing apparatus 2 in the sequence described below. After the formation of the film, the inside of the film formation apparatus 1 is evacuated to a sufficiently high vacuum. Also, the preliminary chamber, indicated by 9, is evacuated to a sufficiently high vacuum. A gate mounted between the film formation chamber 1 and the preliminary chamber is opened, followed by shift of the substrate into the preliminary chamber. Thereafter, the gate is closed. A reactive gas is again introduced into the film formation apparatus to start growth of a film.
At this time, the inside of the laser processing apparatus 2 is evacuated to a sufficiently high vacuum. The inside of the preliminary chamber 9 has been already maintained as a sufficiently high vacuum. The gate between the preliminary chamber and the laser processing apparatus is opened, and then the substrate is transported from the preliminary chamber into the laser processing apparatus. Subsequently, the gate is closed. The sample holder 15 is heated to an appropriate temperature by the heater 16. After the temperature has stabilized and the substrate set in the laser processing apparatus has been accurately aligned, laser processing is carried out.
At this time, if the time required for the laser processing apparatus to process one substrate (including operations for placing the substrate in position, aligning, and taking out the substrate) is substantially equal to the time required for the plasma CVD apparatus to form a film (including operations for placing the substrate in position and evacuating the inside), then no waiting time is necessary between the processing performed by the plasma CVD apparatus and the processing conducted by the laser processing apparatus. If the time taken to process one substrate by laser light is half of the time taken to form a film by the plasma CVD apparatus, then the film may be formed on two substrates in one operation by the plasma CVD apparatus. In this case, after completion of the film, the two substrates are moved into the preliminary chamber. One of them is transported into the laser processing apparatus where the substrate is processed. The other is preserved in the preliminary chamber. After the first one is processed, the one preserved in the preliminary chamber is processed.
Referring to
The plasma doping apparatus and the laser annealing apparatus have chambers 21 and 22, respectively. These chambers are designed so that requisite gases can be introduced into them and that unwanted gases can be expelled from them. Also, the pressure inside each chamber can be maintained at an appropriate value.
The chamber 21 is further equipped with an anode electrode 24 and a grid electrode 25. A high voltage which can be increased up to 100 kV is applied to the anode from a high voltage source 23. A plasma is produced around the grid electrode by RF discharge and contains positive ions 26. These ions 26 are accelerated toward a sample holder 28 by the high voltage described above. As a result, accelerated positive ions are implanted into a substrate or sample 27 lying on the sample holder 28.
This ion implantation changes the state of the crystalline material such as a single crystal of silicon or crystalline silicon formed on the substrate into an amorphous or almost amorphous state. In consequence, the electrical characteristics are deteriorated. Therefore, the substrate is crystallized by laser annealing to improve the characteristics. The chamber 22 is provided with a window 34. Laser light emitted from a laser 31 passes through the window 34 via a mirror 32 and a lens 33 and impinges on a substrate 35 that is placed on a sample holder 36. The substrate may be heated by a heater 37. The sample holder is capable of moving gradually to the right as viewed in the figure while carrying the substrate. As a result, the whole surface of the substrate can be processed by the laser light. The substrate doped by the plasma doping apparatus 21 is moved into the laser processing apparatus 22 via the preliminary chamber 29, in the same way as in Example 1.
In the present example, the doping apparatus makes use of ion implantation which uses a plasma source. Obviously, the doping apparatus can be replaced by an ion implanter which separates ions according to their masses and implants them into the substrate.
Referring next to
The plasma doping apparatus, the etching apparatus, and the laser annealing apparatus have chambers 41, 42, and 43, respectively. These chambers are designed so that requisite gases can be introduced into them and that unwanted gases can be discharged from them. Also, the pressure inside each chamber can be maintained at an appropriate value.
The chamber 41 is further equipped with an anode electrode 45 and a grid electrode 46. A high voltage which can be increased up to 100 kV is applied to the anode from a high voltage source 44. A plasma is produced around the grid electrode by RF discharge and contains positive ions 47. These ions 47 are accelerated toward a sample holder 49 by the high voltage described above. As a result, accelerated positive ions such as boron ions or phosphorus ions are implanted into the substrate or sample 48 lying on the sample holder 49.
For example, it is assumed that a layer of crystalline silicon is formed on the insulating substrate 48 and that a layer of silicon oxide is formed on the layer of crystalline silicon. Also, it is assumed that gate electrodes of thin-film transistors are formed. Desired impurities are implanted into the silicon oxide layer and the silicon layer by this doping method. This method is adequate to form semiconductor devices with high production yield because the doping is carried out through the material such as silicon oxide.
As already described in Example 2, this ion implantation deteriorates the crystallinity and hence the crystallinity is improved by laser annealing or other method. An impurity is also injected into the silicon oxide. Where a UV excimer laser adapted for mass production such as a KrF laser emitting a wavelength of 248 nm, an XeCl laser emitting a wavelength of 308 nm, or an XeF laser emitting a wavelength of 350 nm is used for the laser annealing, a problem takes place. In particular, pure silicon oxide is transparent to UV light of wavelengths exceeding 200 nm but silicon oxide containing impurities absorbs such UV light to a considerable extent. As a result, a major part of the laser energy is absorbed by the silicon oxide film. This makes it impossible to use the laser energy efficiently in improving the crystallinity. To solve this problem, the silicon oxide film is etched so that laser radiation may be efficiently absorbed by the film whose crystallinity should be improved. The etching apparatus 42 is provided for this purpose.
The etching apparatus 42 is equipped with electrodes 53 and 54. An RF power supply 52 is connected with the electrode 53. A substrate 55 is placed on the electrode 54. As an example, if an electric discharge is produced between the electrodes by electric power from the RF power supply within an ambient of carbon tetrafluoride, then the silicon oxide film on the substrate can be etched.
The laser processing apparatus 43 is substantially the same as the laser processing apparatus described in Examples 1 and 2. The chamber 43 is provided with a window 61. Laser light emitted from a laser 58 passes through the window 61 via a mirror 59 and a lens 60 and impinges on a substrate 62 lying on a movable sample holder 64. The substrate may be heated by a heater 63.
The substrate doped by the plasma doping apparatus 21 is transported into the etching apparatus 42 via a preliminary chamber 50 in the same way as in Example 1. After end of etching processing, the substrate is moved into the laser processing apparatus 43 via the preliminary chamber 56.
An example of fabrication of thin-film transistors (TFTs), using such a multi-chamber system, is described by referring to
The crystallized silicon film is patterned into N-type regions 103 and P-type regions 104. A silicon oxide film 105 having a thickness of 50 to 150 nm and acting as a gate oxide film is formed. Then, gate electrodes 106 and 107 are fabricated from aluminum, tantalum, chromium, tungsten, molybdenum, silicon, an alloy of some of them, or the material of multilayer conductive interconnects (FIG. 5(A)).
Then, a masking material 108 such as a photoresist is formed only on the N-type regions 103. Boron ions are implanted by the plasma doping apparatus 41 shown in FIG. 3. The boron ions are accelerated at an accelerating voltage of 20 to 65 keV, typically 65 keV. The dose is 6×1015 atoms/cm2. P-type regions 109 are formed by this doping process (FIG. 5(B)).
After the end of the doping process, the substrate is conveyed into the etching apparatus 42, where the masking material 108 is removed by electric discharge within an ambient of oxygen. Usually, a high efficiency would be obtained by peeling the masking material such as a photoresist with a peeling liquid. However, where moving the substrate into and out of a vacuum apparatus is taken into account, ashing by the etching apparatus will give a high efficiency to the multi-chamber system shown in FIG. 3. Also, a high throughput will be derived.
The substrate is returned to the doping apparatus 41, where phosphorus atoms are implanted. The phosphorus atoms are accelerated at an accelerating voltage of 20 to 85 keV, typically 80 keV. The dose is 4×1015 atoms/cm2. N-type regions 110 are formed by this doping process (FIG. 5(C)).
Then, the substrate is again transported into the etching apparatus 42, where the silicon oxide film 105 is etched. As described previously, large amounts of phosphorous and boron are contained in the silicon oxide film. Laser light is strongly absorbed by the silicon oxide film. This makes it impossible to conduct laser annealing efficiently (FIG. 5(D)).
After the silicon oxide film 105 is etched, the substrate is transported into the laser processing apparatus 43, where laser annealing is conducted. A KrF laser emitting laser radiation having a pulse width of 20 nsec and a repetition frequency of 200 Hz is used for the laser annealing. Obviously, other kind of laser can also be employed. The energy density per pulse of laser beam is 200 to 400 mJ/cm2, preferably 250 to 300 mJ/cm2. This energy density is modified according to other conditions such as the dose and the thickness of the silicon film (FIG. 5(E)).
After completion of the laser annealing, the substrate is taken out, and an interlayer insulating film 111 and metal interconnects-and-electrodes 112 are formed. Of course, a film formation chamber may be added to the multi-chamber system of
In
Substrates 81-84 are transported into the preliminary chamber and other chamber by a robot arm 80. This system can be expanded as the need arises. During mass production, flexibility (e.g., capability of adding a film formation step and an etching step and flexibility given to modification of tact arising from elongation of the film formation time) can be enhanced.
Referring to
The chamber 601 for conducting a rapid thermal anneal comprises a light source or lamp 602 emitting infrared light, the chamber 603 forming a light source chamber, and a quartz window 606 transmitting infrared light. The chamber 601 is further provided with a gas intake system (not shown) for introducing inert gas and requisite gases and also with a gas exhaust system (not shown).
A substrate 604 is placed on a substrate holder 605 and transported into the various chambers by a robot arm, or a robot hand for transporting substrates. The substrate may be transported alone or together with the substrate holder.
It is common practice to conduct a rapid thermal anneal within an ambient of an inert gas such as nitrogen. Alternatively, the anneal may be carried out within an ambient of ammonia (NH3), nitrous oxide (N2O), or oxygen.
An example using an apparatus shown in
The inside of the chamber 601 is evacuated. The substrate is transported into the preliminary chamber 56 the inside of which is maintained substantially at the same subatmospheric pressure as the pressure inside the chamber 601. The substrate is conveyed into the chamber 41, where a plasma doping process is effected, via the chamber 42 and the preliminary chamber 50 which are similarly maintained at subatmospheric Pressure. It is important that these steps for conveying the substrate be carried out without exposing the substrate to outside air.
A required ion implantation step is performed inside the chamber of the doping apparatus. The substrate is then moved into the chamber 42 of the etching apparatus while maintaining the degree of vacuum. A dry etching process is carried out to remove the exposed oxide film 105. The substrate is transported into the chamber 601, where a rapid thermal anneal is effected to activate the implanted impurity. At this time, the absence of the oxide film 105 is important for efficient achievement of the rapid thermal anneal. In particular, the impurity lodged at the time of the ion implantation exists inside the silicon oxide film 105, and this impurity absorbs infrared light.
The structure of the apparatus described thus far may be replaced by a combination of a chamber for illuminating laser radiation and a chamber where a rapid thermal anneal is conducted. Furthermore, a plurality of chambers required may be combined.
In the present invention, a laser processing apparatus is combined with associated vacuum apparatus such as a film formation apparatus and an etching apparatus to form a system. This system is efficiently utilized to provide improved productivity. In this way, the invention is industrially advantageous.
Number | Date | Country | Kind |
---|---|---|---|
4-350546 | Dec 1992 | JP | national |
5-301172 | Nov 1993 | JP | national |
This application is a Continuation of Ser. No. 08/160,909, filed Dec. 3, 1993, now abandoned.
Number | Name | Date | Kind |
---|---|---|---|
4151058 | Kaplan et al. | Apr 1979 | A |
4226898 | Ovshinsky et al. | Oct 1980 | A |
4313783 | Davies et al. | Feb 1982 | A |
4322253 | Pankove et al. | Mar 1982 | A |
4370175 | Levatter | Jan 1983 | A |
4388145 | Hawkins et al. | Jun 1983 | A |
4402762 | John et al. | Sep 1983 | A |
4405435 | Tateishi et al. | Sep 1983 | A |
4475027 | Pressley | Oct 1984 | A |
4482395 | Hiramoto | Nov 1984 | A |
4498416 | Bouchaib | Feb 1985 | A |
4503807 | Nakayama et al. | Mar 1985 | A |
4523370 | Sullivan et al. | Jun 1985 | A |
4552595 | Hoga | Nov 1985 | A |
4557036 | Kyuragi et al. | Dec 1985 | A |
4567061 | Hayashi et al. | Jan 1986 | A |
4576851 | Iwamatsu | Mar 1986 | A |
4582720 | Yamazaki | Apr 1986 | A |
4589951 | Kawamura | May 1986 | A |
4590091 | Rogers, Jr. et al. | May 1986 | A |
4592306 | Gallego | Jun 1986 | A |
4592799 | Hayafuji | Jun 1986 | A |
4595601 | Horioka et al. | Jun 1986 | A |
4609407 | Masao et al. | Sep 1986 | A |
4640223 | Dozier | Feb 1987 | A |
4663829 | Hartman et al. | May 1987 | A |
4694143 | Nishimura et al. | Sep 1987 | A |
4698486 | Sheets | Oct 1987 | A |
4699863 | Sawatari et al. | Oct 1987 | A |
4719123 | Haku et al. | Jan 1988 | A |
4727044 | Yamazaki | Feb 1988 | A |
4800174 | Ishihara et al. | Jan 1989 | A |
4808554 | Yamazaki | Feb 1989 | A |
4843022 | Yamazaki | Jun 1989 | A |
4888305 | Yamazaki et al. | Dec 1989 | A |
4937205 | Nakayama et al. | Jun 1990 | A |
4951601 | Maydan et al. | Aug 1990 | A |
4986213 | Yamazaki et al. | Jan 1991 | A |
4988642 | Yamazaki | Jan 1991 | A |
5091334 | Yamazaki et al. | Feb 1992 | A |
5141058 | Heppner | Aug 1992 | A |
5171710 | Yamazaki et al. | Dec 1992 | A |
5174881 | Iwasaki et al. | Dec 1992 | A |
5186718 | Tepman et al. | Feb 1993 | A |
5194398 | Miyachi et al. | Mar 1993 | A |
5200017 | Kawasaki et al. | Apr 1993 | A |
5266116 | Fujioka et al. | Nov 1993 | A |
5286296 | Sato et al. | Feb 1994 | A |
5288658 | Ishihara | Feb 1994 | A |
5292393 | Maydan et al. | Mar 1994 | A |
5292675 | Codama | Mar 1994 | A |
5296405 | Yamazaki et al. | Mar 1994 | A |
5304357 | Sato et al. | Apr 1994 | A |
5310410 | Begin et al. | May 1994 | A |
5314538 | Maeda et al. | May 1994 | A |
5314839 | Mizutani et al. | May 1994 | A |
5316960 | Watanabe et al. | May 1994 | A |
5324360 | Kozuka | Jun 1994 | A |
5344522 | Yagi et al. | Sep 1994 | A |
5490896 | Yagi et al. | Feb 1996 | A |
5535884 | Scott et al. | Jul 1996 | A |
5545571 | Yamazaki et al. | Aug 1996 | A |
5753542 | Yamazaki et al. | May 1998 | A |
5804471 | Yamazaki et al. | Sep 1998 | A |
5811327 | Funai et al. | Sep 1998 | A |
6177302 | Yamazaki et al. | Jan 2001 | B1 |
6261877 | Yamazaki et al. | Jul 2001 | B1 |
6329229 | Yamazaki et al. | Dec 2001 | B1 |
6482752 | Yamazaki et al. | Nov 2002 | B1 |
6566175 | Yamazaki et al. | May 2003 | B1 |
Number | Date | Country |
---|---|---|
2 116 634 | Jan 1987 | EP |
60-042817 | Jan 1985 | JP |
62-54423 | Mar 1987 | JP |
62-54448 | Mar 1987 | JP |
62-104117 | May 1987 | JP |
63-160336 | Jul 1988 | JP |
63-318125 | Dec 1988 | JP |
64-76715 | Mar 1989 | JP |
1-179410 | Jul 1989 | JP |
02-033934 | Feb 1990 | JP |
2-73623 | Mar 1990 | JP |
2-081424 | Mar 1990 | JP |
2-239615 | Sep 1990 | JP |
03-042868 | Feb 1991 | JP |
3-082121 | Apr 1991 | JP |
03-095965 | Apr 1991 | JP |
03-201538 | Sep 1991 | JP |
3-286518 | Dec 1991 | JP |
04-022127 | Jan 1992 | JP |
04-063414 | Feb 1992 | JP |
04-221854 | Aug 1992 | JP |
4-251921 | Sep 1992 | JP |
04-278925 | Oct 1992 | JP |
04-286367 | Oct 1992 | JP |
04-286370 | Oct 1992 | JP |
04-332130 | Nov 1992 | JP |
05-021382 | Jan 1993 | JP |
5-206063 | Aug 1993 | JP |
05-259259 | Oct 1993 | JP |
Number | Date | Country | |
---|---|---|---|
Parent | 08160909 | Dec 1993 | US |
Child | 08691434 | US |