CA2284475C - Growth of gan on sapphire with mse grown buffer layer - Google Patents
Growth of gan on sapphire with mse grown buffer layer Download PDFInfo
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- CA2284475C CA2284475C CA 2284475 CA2284475A CA2284475C CA 2284475 C CA2284475 C CA 2284475C CA 2284475 CA2284475 CA 2284475 CA 2284475 A CA2284475 A CA 2284475A CA 2284475 C CA2284475 C CA 2284475C
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- sapphire
- buffer layer
- gan
- mse
- growth
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- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B23/00—Single-crystal growth by condensing evaporated or sublimed materials
- C30B23/02—Epitaxial-layer growth
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B29/00—Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
- C30B29/10—Inorganic compounds or compositions
- C30B29/40—AIIIBV compounds wherein A is B, Al, Ga, In or Tl and B is N, P, As, Sb or Bi
- C30B29/403—AIII-nitrides
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B29/00—Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
- C30B29/10—Inorganic compounds or compositions
- C30B29/40—AIIIBV compounds wherein A is B, Al, Ga, In or Tl and B is N, P, As, Sb or Bi
- C30B29/403—AIII-nitrides
- C30B29/406—Gallium nitride
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- Engineering & Computer Science (AREA)
- Crystallography & Structural Chemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Physical Deposition Of Substances That Are Components Of Semiconductor Devices (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
Abstract
A method of fabricating a gallium nitride or like epilayer on sapphire is disclosed wherein a buffer layer is grown on the sapphire substrate by magnetron sputter epitaxy (MSE); and then the gallium nitride epilayer is formed on the buffer layer, preferably by molecular beam epitaxy.
Description
GROWTH OF GaN ON SAPPHIRE WITH MSE GROWN BUFFER LAYER
Field of the Invention This invention relates to the growth of gallium arsenide and like materials on a sapphire substrate.
Background of the Invention In recent years there has been tremendous interest in GaN based III-N
materials. A
dramatic improvement in the material quality has led to the development of high brightness light emitting diodes, and more recently "blue" laser diodes. There has also been a dramatic improvement in the performance of high power microwave metal-semiconductor field-effect transistors and modulation doped field-effect transistors based on these materials.
Crucial to all these applications is the growth of material with high crystalline quality and of high purity. Various techniques have been used to grow GaN including metalorganic vapor phase epitaxy (MOVPE), plasma molecular beam epitaxy (plasma-MBE), ammonia molecular beam epitaxy (ammonia-MBE), also referred to as reactive molecular beam epitaxy, and magnetron sputter epitaxy (MSE). Typically GaN epilayers are grown on sapphire substrates, which are highly lattice mismatched, necessitating the predeposition of a thin (-'500 hi) buffer/nucleation layer of either GaN or AIN. The observed electrical and optical properties of the resulting GaN layers is strongly dependent on the dislocation density and of the overall impurity content.
Using these growth techniques, room temperature electron mobilities for MOVPE-grown silicon doped GaN layers are typically reported in the range of 350-600 cm2N
s. The highest room temperature mobility ever reported for GaN was 900 cm2N s deposited by MOVPE for a 4 m thick layer. MOVPE is however disadvantageous in that it requires a dedicated nitrogen source and allows deposition of GaN over a limited range of growth temperatures. In contrast, the highest room temperature mobility for plasma-MBE grown GaN is around 300 cmZN s and for ammonia-MBE is 350 cm2N s.
Summary of the Invention According to the present invention there is provided a method of fabricating an epilayer -~-on sapphire, comprising the steps of providing a sapphire substrate; growing an A1N
buffer layer on said sapphire substrate by magnetron sputter epitaxy (MSE) to reduce lattice mismatch; and subsequently forming said epilayer on said A1N buffer layer.
Using this method, silicon doped GaN epilayers having room temperature electron mobilities >550 cmZ/V s can be grown on grown on (0001) sapphire. Unlike other growth techniques, the initial buffer/nucleation layer, preferably of A1N (aluminum nitride), is grown by MSE.
The deposition of the GaN layers may be performed in a dual mode MBE/MSE
system.
The MSE technique differs from conventional MBE in that an ultrahigh vacuum dc magnetron sputter cathode is used as the group III source and deposition of the layers occurs in the pressure range of 1-5 mTorr.
Typically, the MSE technique is employed only for the growth of the buffer/nucleation layer. The GaN layer is deposited by ammonia MBE where a conventional dual filament K cell is used for the gallium source, and high purity ammonia is used as the source of nitrogen.
Preferably, the deposition system is equipped with a substrate holder capable of heating the 2 in. sapphire (0001) wafers to temperatures in excess of 1000 C. Typical growth temperatures for the GaN layers were in the range of 860-920 C as measured by an optical pyrometer (emissivity set to 0.3).
Brief Description of the Drawings The invention will now be described in more detail, by way of example only, with reference to the accompanying drawings, in which;-Figure 1 is a schematic diagram of an MSE system;
Figure 2 is a plot showing photoluminescent intensity against energy for a 2.2 thick GaN
epilayer on (0001) sapphire at 4K and room temperature; and Figure 3 shows the Hall effect carrier mobility and carrier density for a 2.3 m thick GaN
epilayer on (0001) sapphire for temperatures in the range 77 to 300 K.
Description of the Preferred Embodiments The dual MBE (molecular beam epitaxy)/MSE system shown in Figure 1 comprises a vacuum chamber 10 with a nitrogen cryoshroud 12, and port 14 for K-cells, port 16 for a 3-source alkyl/gas injection cell, and port(s) 18 for modified-UHV magnetron sputter sources, such as aluminum. Cryopump 20 is connected to the chamber 10.
The main chamber 10 is cryo/turbopumped to a base pressure of < 5 x 10-11 torr.
Substrates up to 4" diameter are introduced into the main chamber via a load-lock and transfer arm. A BN coated graphite heater is used to heat substrates up to 1200 C.
Substrates are typically 2" (0001)sapphire coated on the back surface with molybdenum.
Smaller pieces are mounted using indium solder to a 2" silicon wafer.
With this system, a solid MBE-grade aluminum source can be D.C. sputtered using an argon plasma operating at 1-3 mtorr [target power of 50 Watts, 400 Volts].
High purity ammonia introduced via the gas injection cell is used as the nitrogen source [flow of 15 sccm]. The magnetron plasma is sufficient to provide a source of nitrogen ions for the growth of A1N. Growth rates for the MSE grown A1N buffer layer at 880 are typically 0.15 to 0.25 m/hr.
Example Sapphire wafers (backside sputter coated with Mo) were degreased in chloroform vapor followed by a 1 min dip in 10% HF, then rinsed in deionized water and blown dry with nitrogen gas. The substrate was then introduced into the system load-lock where degassing of the wafer was carried out before introduction into the growth chamber 10.
The growth chamber was fully cryoshrouded with a base pressure of <10-9Torr.
The substrate was then heated to a telnperature of 1000 C under 130 sccm of ammonia for 10 min before cooling to the buffer layer growth temperature of 880 C.
The buffer or nucleation layer of A1N was used. This layer was deposited by MSE using a high purity Al magnetron sputter cathode and ammonia. The growth of the nucleation and epilayer was monitored using in situ laser reflectance spectrometry. A 200 A
nucleation layer was deposited at a growth rate of 34 A/min with argon and ammonia flows of 40 and 15 sccm, respectively. This resulted in a deposition pressure of about 1.4 mTorr.
Following the deposition of the A1N nucleation layer, the substrate was then heated to the GaN epilayer growth temperature. The Ga K-cell temperature was adjusted to give a growth rate of from 1-2 m/h at an ammonia flow rate of 50 sccm. Typical base pressures of 3 x 10"6 Torr were observed during growth. Both undoped and silicon doped layers _.
were grown. For the doped layers, silane was used as the dopant source. The formed GaN
layers had thicknesses of -2 m.
The epilayers were characterized using a triple axis x-ray diffractometer c) and c) - 20 scans were carried out to determine both the mosaicity and crystalline quality of the deposited layers. Hall effect mobilities and carrier densities were measured using a van der Pauw geometry (sample size of -0.5 xO.5 cm, applied field of 3 kG) with soldered indium dots as the ohmic contacts. The contacts were verified to be ohmic by I-V
measurements. Photoluminescence (PL) was performed at room temperature (RT) and 4 K using excitation from a He-Cd laser with an incident power density of < 0.25 W/cm2.
Table 1 gives the observed x-ray linewidths and electrical data for a number of layers grown at several different temperatures. All data shown in Table I are for layers that were intentionally doped to 1-7 x 1017cm 3. As shown in Table 1, the minimum linewidths for the co and co - 20 scans were 210 and 13.7 arcsec, respectively, with the highest observed mobility of 560 cm2/V s for a carrier density of 1.44 x 1017cm 3.
Table 1 X-ray X-ray Electron Layer o)scan w 20 scan Carrier density mobility No. (aresec) (arcsec) n (x 1017crri 3) (cmI/Vs) 1 210 13.7 X.5 356 2 271 17.0 7.0 400 3 299 14.8 7.0 340 4 377 15.8 3.5 407 5 303 14.2 1.4 560 6 324 14.5 1.6 547 7 323 14.9 1.3 544 Figure 2 gives a plot of the observed PL spectrum for a representative layer of GaN. As shown in Fig. 2, even at very low excitation intensities the yellow luminescence band is very weak at room temperature and virtually absent at 4 K. The spectra are dominated by strong donor-bound exciton emissions at 3.48 and 3.42 eV with FWHM of 4.9 and meV for temperatures of 4 K and room temperature, respectively. At 4 K only very weak emission from donor-acceptor transitions are observed, which would indicate a low density of defects and/or impurities. This is consistent with the observed high mobilities and correspondingly low compensation for these layers.
Figure 3 shows the measured mobility and carrier density of a representative GaN layer.
As shown in Fig. 3, a peak mobility of 952 cm2/V s is observed at a temperature of 145 K. The corresponding carrier density shows a single activation energy of about 13 meV, which is similar to that observed previously for silicon doped GaN.
By the described technique, MBE, GaN layers with electron mobilities of up to cm2/V s can be successfully grown with good reproducibility. This indicates that using the MBE technique with an MSE grown A1N buffer layer, the type of defects affecting the electron mobility can be reduced significantly as they have been using MOVPE but without the attendant disadvantages of MOVPE.
Field of the Invention This invention relates to the growth of gallium arsenide and like materials on a sapphire substrate.
Background of the Invention In recent years there has been tremendous interest in GaN based III-N
materials. A
dramatic improvement in the material quality has led to the development of high brightness light emitting diodes, and more recently "blue" laser diodes. There has also been a dramatic improvement in the performance of high power microwave metal-semiconductor field-effect transistors and modulation doped field-effect transistors based on these materials.
Crucial to all these applications is the growth of material with high crystalline quality and of high purity. Various techniques have been used to grow GaN including metalorganic vapor phase epitaxy (MOVPE), plasma molecular beam epitaxy (plasma-MBE), ammonia molecular beam epitaxy (ammonia-MBE), also referred to as reactive molecular beam epitaxy, and magnetron sputter epitaxy (MSE). Typically GaN epilayers are grown on sapphire substrates, which are highly lattice mismatched, necessitating the predeposition of a thin (-'500 hi) buffer/nucleation layer of either GaN or AIN. The observed electrical and optical properties of the resulting GaN layers is strongly dependent on the dislocation density and of the overall impurity content.
Using these growth techniques, room temperature electron mobilities for MOVPE-grown silicon doped GaN layers are typically reported in the range of 350-600 cm2N
s. The highest room temperature mobility ever reported for GaN was 900 cm2N s deposited by MOVPE for a 4 m thick layer. MOVPE is however disadvantageous in that it requires a dedicated nitrogen source and allows deposition of GaN over a limited range of growth temperatures. In contrast, the highest room temperature mobility for plasma-MBE grown GaN is around 300 cmZN s and for ammonia-MBE is 350 cm2N s.
Summary of the Invention According to the present invention there is provided a method of fabricating an epilayer -~-on sapphire, comprising the steps of providing a sapphire substrate; growing an A1N
buffer layer on said sapphire substrate by magnetron sputter epitaxy (MSE) to reduce lattice mismatch; and subsequently forming said epilayer on said A1N buffer layer.
Using this method, silicon doped GaN epilayers having room temperature electron mobilities >550 cmZ/V s can be grown on grown on (0001) sapphire. Unlike other growth techniques, the initial buffer/nucleation layer, preferably of A1N (aluminum nitride), is grown by MSE.
The deposition of the GaN layers may be performed in a dual mode MBE/MSE
system.
The MSE technique differs from conventional MBE in that an ultrahigh vacuum dc magnetron sputter cathode is used as the group III source and deposition of the layers occurs in the pressure range of 1-5 mTorr.
Typically, the MSE technique is employed only for the growth of the buffer/nucleation layer. The GaN layer is deposited by ammonia MBE where a conventional dual filament K cell is used for the gallium source, and high purity ammonia is used as the source of nitrogen.
Preferably, the deposition system is equipped with a substrate holder capable of heating the 2 in. sapphire (0001) wafers to temperatures in excess of 1000 C. Typical growth temperatures for the GaN layers were in the range of 860-920 C as measured by an optical pyrometer (emissivity set to 0.3).
Brief Description of the Drawings The invention will now be described in more detail, by way of example only, with reference to the accompanying drawings, in which;-Figure 1 is a schematic diagram of an MSE system;
Figure 2 is a plot showing photoluminescent intensity against energy for a 2.2 thick GaN
epilayer on (0001) sapphire at 4K and room temperature; and Figure 3 shows the Hall effect carrier mobility and carrier density for a 2.3 m thick GaN
epilayer on (0001) sapphire for temperatures in the range 77 to 300 K.
Description of the Preferred Embodiments The dual MBE (molecular beam epitaxy)/MSE system shown in Figure 1 comprises a vacuum chamber 10 with a nitrogen cryoshroud 12, and port 14 for K-cells, port 16 for a 3-source alkyl/gas injection cell, and port(s) 18 for modified-UHV magnetron sputter sources, such as aluminum. Cryopump 20 is connected to the chamber 10.
The main chamber 10 is cryo/turbopumped to a base pressure of < 5 x 10-11 torr.
Substrates up to 4" diameter are introduced into the main chamber via a load-lock and transfer arm. A BN coated graphite heater is used to heat substrates up to 1200 C.
Substrates are typically 2" (0001)sapphire coated on the back surface with molybdenum.
Smaller pieces are mounted using indium solder to a 2" silicon wafer.
With this system, a solid MBE-grade aluminum source can be D.C. sputtered using an argon plasma operating at 1-3 mtorr [target power of 50 Watts, 400 Volts].
High purity ammonia introduced via the gas injection cell is used as the nitrogen source [flow of 15 sccm]. The magnetron plasma is sufficient to provide a source of nitrogen ions for the growth of A1N. Growth rates for the MSE grown A1N buffer layer at 880 are typically 0.15 to 0.25 m/hr.
Example Sapphire wafers (backside sputter coated with Mo) were degreased in chloroform vapor followed by a 1 min dip in 10% HF, then rinsed in deionized water and blown dry with nitrogen gas. The substrate was then introduced into the system load-lock where degassing of the wafer was carried out before introduction into the growth chamber 10.
The growth chamber was fully cryoshrouded with a base pressure of <10-9Torr.
The substrate was then heated to a telnperature of 1000 C under 130 sccm of ammonia for 10 min before cooling to the buffer layer growth temperature of 880 C.
The buffer or nucleation layer of A1N was used. This layer was deposited by MSE using a high purity Al magnetron sputter cathode and ammonia. The growth of the nucleation and epilayer was monitored using in situ laser reflectance spectrometry. A 200 A
nucleation layer was deposited at a growth rate of 34 A/min with argon and ammonia flows of 40 and 15 sccm, respectively. This resulted in a deposition pressure of about 1.4 mTorr.
Following the deposition of the A1N nucleation layer, the substrate was then heated to the GaN epilayer growth temperature. The Ga K-cell temperature was adjusted to give a growth rate of from 1-2 m/h at an ammonia flow rate of 50 sccm. Typical base pressures of 3 x 10"6 Torr were observed during growth. Both undoped and silicon doped layers _.
were grown. For the doped layers, silane was used as the dopant source. The formed GaN
layers had thicknesses of -2 m.
The epilayers were characterized using a triple axis x-ray diffractometer c) and c) - 20 scans were carried out to determine both the mosaicity and crystalline quality of the deposited layers. Hall effect mobilities and carrier densities were measured using a van der Pauw geometry (sample size of -0.5 xO.5 cm, applied field of 3 kG) with soldered indium dots as the ohmic contacts. The contacts were verified to be ohmic by I-V
measurements. Photoluminescence (PL) was performed at room temperature (RT) and 4 K using excitation from a He-Cd laser with an incident power density of < 0.25 W/cm2.
Table 1 gives the observed x-ray linewidths and electrical data for a number of layers grown at several different temperatures. All data shown in Table I are for layers that were intentionally doped to 1-7 x 1017cm 3. As shown in Table 1, the minimum linewidths for the co and co - 20 scans were 210 and 13.7 arcsec, respectively, with the highest observed mobility of 560 cm2/V s for a carrier density of 1.44 x 1017cm 3.
Table 1 X-ray X-ray Electron Layer o)scan w 20 scan Carrier density mobility No. (aresec) (arcsec) n (x 1017crri 3) (cmI/Vs) 1 210 13.7 X.5 356 2 271 17.0 7.0 400 3 299 14.8 7.0 340 4 377 15.8 3.5 407 5 303 14.2 1.4 560 6 324 14.5 1.6 547 7 323 14.9 1.3 544 Figure 2 gives a plot of the observed PL spectrum for a representative layer of GaN. As shown in Fig. 2, even at very low excitation intensities the yellow luminescence band is very weak at room temperature and virtually absent at 4 K. The spectra are dominated by strong donor-bound exciton emissions at 3.48 and 3.42 eV with FWHM of 4.9 and meV for temperatures of 4 K and room temperature, respectively. At 4 K only very weak emission from donor-acceptor transitions are observed, which would indicate a low density of defects and/or impurities. This is consistent with the observed high mobilities and correspondingly low compensation for these layers.
Figure 3 shows the measured mobility and carrier density of a representative GaN layer.
As shown in Fig. 3, a peak mobility of 952 cm2/V s is observed at a temperature of 145 K. The corresponding carrier density shows a single activation energy of about 13 meV, which is similar to that observed previously for silicon doped GaN.
By the described technique, MBE, GaN layers with electron mobilities of up to cm2/V s can be successfully grown with good reproducibility. This indicates that using the MBE technique with an MSE grown A1N buffer layer, the type of defects affecting the electron mobility can be reduced significantly as they have been using MOVPE but without the attendant disadvantages of MOVPE.
Claims (7)
1. A method of fabricating an epilayer on sapphire, comprising the steps of:
providing a sapphire substrate;
growing an A1N buffer layer on said sapphire substrate by magnetron sputter epitaxy (MSE) to reduce lattice mismatch; and subsequently forming said epilayer on said A1N buffer layer.
providing a sapphire substrate;
growing an A1N buffer layer on said sapphire substrate by magnetron sputter epitaxy (MSE) to reduce lattice mismatch; and subsequently forming said epilayer on said A1N buffer layer.
2. A method as claimed in claim 1, wherein said buffer layer is 100 to 500A
thick.
thick.
3. A method as claimed in claim 1 or 2, wherein said epilayer is a gallium nitride.
4. A method as claimed in claim 3, wherein said gallium nitride epilayer is grown at a temperature of about 860 - 920°C.
5. A method as claimed in any one of claims 1 to 4, wherein said substrate is (0001) sapphire.
6. A method as claimed in any one of claims 1 to 5, wherein said AIN layer is deposited at a growth rate of about 0.25 µm/hr with argon and ammonia flows of about 40 and 15 sccm respectively at a deposition pressure of about 1.4mTorr.
7. A method as claimed in claim 3, wherein said gallium nitride layer is grown by molecular beam epitaxy (MBE) on said buffer layer.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA 2284475 CA2284475C (en) | 1999-10-04 | 1999-10-04 | Growth of gan on sapphire with mse grown buffer layer |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA 2284475 CA2284475C (en) | 1999-10-04 | 1999-10-04 | Growth of gan on sapphire with mse grown buffer layer |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2284475A1 CA2284475A1 (en) | 2001-04-04 |
| CA2284475C true CA2284475C (en) | 2008-09-09 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA 2284475 Expired - Fee Related CA2284475C (en) | 1999-10-04 | 1999-10-04 | Growth of gan on sapphire with mse grown buffer layer |
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| Country | Link |
|---|---|
| CA (1) | CA2284475C (en) |
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1999
- 1999-10-04 CA CA 2284475 patent/CA2284475C/en not_active Expired - Fee Related
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| Publication number | Publication date |
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| CA2284475A1 (en) | 2001-04-04 |
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