CA2211028C - Process and apparatus for manufacturing polycrystalline silicon, and process for manufacturing silicon wafer for solar cell - Google Patents
Process and apparatus for manufacturing polycrystalline silicon, and process for manufacturing silicon wafer for solar cell Download PDFInfo
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- CA2211028C CA2211028C CA002211028A CA2211028A CA2211028C CA 2211028 C CA2211028 C CA 2211028C CA 002211028 A CA002211028 A CA 002211028A CA 2211028 A CA2211028 A CA 2211028A CA 2211028 C CA2211028 C CA 2211028C
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- 229910052710 silicon Inorganic materials 0.000 title claims abstract description 99
- 239000010703 silicon Substances 0.000 title claims abstract description 99
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 title claims abstract description 97
- 238000000034 method Methods 0.000 title claims abstract description 64
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 54
- 229910021420 polycrystalline silicon Inorganic materials 0.000 title claims abstract description 51
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 40
- 238000007711 solidification Methods 0.000 claims abstract description 37
- 230000008023 solidification Effects 0.000 claims abstract description 37
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims abstract description 30
- 230000001590 oxidative effect Effects 0.000 claims abstract description 25
- 239000012535 impurity Substances 0.000 claims abstract description 24
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 22
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims abstract description 21
- 229910052796 boron Inorganic materials 0.000 claims abstract description 21
- 229910052814 silicon oxide Inorganic materials 0.000 claims abstract description 21
- 238000005520 cutting process Methods 0.000 claims abstract description 16
- 229910052786 argon Inorganic materials 0.000 claims abstract description 15
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 10
- 230000002829 reductive effect Effects 0.000 claims abstract description 8
- 238000007664 blowing Methods 0.000 claims abstract description 7
- 239000001257 hydrogen Substances 0.000 claims abstract description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 7
- 238000005266 casting Methods 0.000 claims abstract description 4
- 239000000155 melt Substances 0.000 claims description 52
- 239000007789 gas Substances 0.000 claims description 36
- 238000003723 Smelting Methods 0.000 claims description 23
- 238000002844 melting Methods 0.000 claims description 22
- 238000010438 heat treatment Methods 0.000 claims description 19
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 13
- 229910052698 phosphorus Inorganic materials 0.000 claims description 13
- 239000011574 phosphorus Substances 0.000 claims description 13
- 230000008018 melting Effects 0.000 claims description 11
- 229910052681 coesite Inorganic materials 0.000 claims description 10
- 229910052906 cristobalite Inorganic materials 0.000 claims description 10
- 229910052682 stishovite Inorganic materials 0.000 claims description 10
- 229910052905 tridymite Inorganic materials 0.000 claims description 10
- 238000001816 cooling Methods 0.000 claims description 9
- 229910002804 graphite Inorganic materials 0.000 claims description 9
- 239000010439 graphite Substances 0.000 claims description 9
- 239000000377 silicon dioxide Substances 0.000 claims description 8
- 238000001704 evaporation Methods 0.000 claims description 6
- 230000008020 evaporation Effects 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 3
- 229910052581 Si3N4 Inorganic materials 0.000 claims description 3
- 229910052802 copper Inorganic materials 0.000 claims description 3
- 239000010949 copper Substances 0.000 claims description 3
- 239000011810 insulating material Substances 0.000 claims description 3
- 238000005507 spraying Methods 0.000 claims description 2
- 235000012239 silicon dioxide Nutrition 0.000 claims 4
- 239000007858 starting material Substances 0.000 abstract description 7
- 229910052751 metal Inorganic materials 0.000 abstract description 4
- 239000002184 metal Substances 0.000 abstract 3
- 239000000758 substrate Substances 0.000 abstract 2
- 239000008246 gaseous mixture Substances 0.000 abstract 1
- 230000003647 oxidation Effects 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 abstract 1
- 238000007670 refining Methods 0.000 abstract 1
- IOVGROKTTNBUGK-SJCJKPOMSA-N ritodrine Chemical compound N([C@@H](C)[C@H](O)C=1C=CC(O)=CC=1)CCC1=CC=C(O)C=C1 IOVGROKTTNBUGK-SJCJKPOMSA-N 0.000 abstract 1
- 235000012431 wafers Nutrition 0.000 description 47
- 238000002360 preparation method Methods 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 239000000126 substance Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- 239000013078 crystal Substances 0.000 description 5
- 238000010310 metallurgical process Methods 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 239000004065 semiconductor Substances 0.000 description 5
- 238000001311 chemical methods and process Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000003344 environmental pollutant Substances 0.000 description 4
- 231100000719 pollutant Toxicity 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 230000005611 electricity Effects 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 238000005229 chemical vapour deposition Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000010894 electron beam technology Methods 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000004857 zone melting Methods 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 241001062472 Stokellia anisodon Species 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000005485 electric heating Methods 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000002440 industrial waste Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920005591 polysilicon Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000013341 scale-up Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000011863 silicon-based powder Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- ZDHXKXAHOVTTAH-UHFFFAOYSA-N trichlorosilane Chemical compound Cl[SiH](Cl)Cl ZDHXKXAHOVTTAH-UHFFFAOYSA-N 0.000 description 1
- 239000005052 trichlorosilane Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- 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
- C30B29/02—Elements
- C30B29/06—Silicon
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B33/00—Silicon; Compounds thereof
- C01B33/02—Silicon
- C01B33/021—Preparation
-
- 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
- C30B11/00—Single-crystal growth by normal freezing or freezing under temperature gradient, e.g. Bridgman-Stockbarger method
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/18—Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof
- H01L31/1804—Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof comprising only elements of Group IV of the Periodic Table
- H01L31/182—Special manufacturing methods for polycrystalline Si, e.g. Si ribbon, poly Si ingots, thin films of polycrystalline Si
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/546—Polycrystalline silicon PV cells
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Electromagnetism (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Manufacturing & Machinery (AREA)
- Inorganic Chemistry (AREA)
- Silicon Compounds (AREA)
Abstract
A process and an apparatus which enables mass production of polycrystalline silicon and a substrate made therefrom at a low cost from metallic silicon or silicon oxide as a starting material in a flow production line involving a series of continuous steps. The polycrystalline silicon and the silicon substrate for solar cells are prepar ed from metallic silicon through step A of refining metallic silicon under reduced pressure and solidifying the metallic silicon to remove impurities from the molten metal, thereby preparing an ingot; step B of cutting and removing an impurity-enriched portion of the ingot; step C of remelting the residue and removing boron and carbon by oxidation from the molten metal under an oxidizing atmosphere, followed by blowing of a gaseous mixture of argon with hydrogen to conduct deoxidation; step D of casting the molten metal after the deoxidation into a mold to conduct unidirectional solidification, thereby preparing an ingot; and step E of cutting and removing an impurity-enriched portion of the ingot prepared by the unidirectional solidification.
Description
PROCESS AND APPARATUS FOR MANUFACTURING POLYCRYSTALLINE
SILICON, AND PROCESS FOR MANUFACTURING SILICON WAFER FOR SOLAR
CELL
BACKGROUND OF THE INVENTION
1. Field of the Invention This invention relates to a process and apparatus for manufacturing polycrystalline silicon and a process for manufacturing a silicon wafer for a solar cell. In particular, this invention pertains to a technique which employs metallic silicon or silicon oxide as a starting material and permits the continuous flow production from polycrystalline silicon to an end product, that is, a polycrystalline silicon wafer for a solar cell.
SILICON, AND PROCESS FOR MANUFACTURING SILICON WAFER FOR SOLAR
CELL
BACKGROUND OF THE INVENTION
1. Field of the Invention This invention relates to a process and apparatus for manufacturing polycrystalline silicon and a process for manufacturing a silicon wafer for a solar cell. In particular, this invention pertains to a technique which employs metallic silicon or silicon oxide as a starting material and permits the continuous flow production from polycrystalline silicon to an end product, that is, a polycrystalline silicon wafer for a solar cell.
2. Description of the Related Art Studies on solar cells have been made for many years.
Recently, those having a photoelectric transfer efficiency of even about 13 to 15% under sun light on the ground have appeared and they are now being industrialized for various applications. In our country, however, solar cells are not so popular as an energy source for domestic electric power, automobiles, ships or machine tools, because a technique to mass-produce a silicon wafer at a low cost, which is necessary for the manufacture of solar cells, has not yet been established.
At present, for the manufacture of a silicon wafer for a solar cell, a high-purity silicon, which is in the mass form and conforms to the specification of a semiconductor, is once manufactured through a chemical process by using as a starting material a low purity metallic silicon (99.5 wt.%
Si). Then, high-purity silicon in the mass form is re-melted and is adjusted to have a chemical composition suited to a solar cell by a metallurgical process. The resulting molten silicon is formed into an ingot by the pulling method or directional solidification method, followed by slicing into thin plates. Described specifically, as shown in FIG S, metallic silicon is first reacted with hydrochloric acid and formed into a trichlorosilane gas. After the gas so obtained is fractionated to remove the impurity elements, the residue is reacted with a hydrogen gas, whereby high-purity silicon is precipitated from the gas by the so-called CVD
(Chemical Vapor Deposition) method. The high-purity silicon therefore becomes only an aggregate of silicon grains owing to the weak bonding power between crystal grains. The boron contained in the high-purity silicon forming the aggregate is reduced even in the order of O.OOI ppm and does not reach the concentration necessary for satisfying the specific resistivity of 0.5 to I.5 ohm~cm which is the specification for P-type semiconductor wafer. In order to use the above high-purity silicon for a solar cell, it is indispensable to adjust the specific resistivity and to control the crystallinity of single crystals or crystal grains so as to . CA 02211028 1997-08-04 have a particle size not smaller than several mm and have a grain boundary so as not to exert adverse effects on the photoelectric transfer efficiency. The above silicon cannot be formed into a wafer without further treatment. As shown in the right hand of FIG. 5, it becomes necessary to form a wafer after re-melting the high-purity silicon mass, adjusting the components of the melt (by the addition of boron) and forming into an ingot (pulling method for single crystals, while directional solidification for polycrystals).
The above-described manufacturing method is however accompanied with the drawbacks that it requires much labor to re-adjust (mainly, by the addition of boron) the components of a silicon ingot, which has a purity intentionally heightened to be suitable for semiconductor, to be suitable for solar cells or to purify the ingot; its yield is inferior; it additionally requires equipment and energy for re-melting; and therefore it costs high. As described above, the solar cells available now are therefore expensive, which prevents them from being popularly used. The purity heightening of metallic silicon by a chemical process is also accompanied with the generation of a large amount of pollutants such as silane and chloride, which prevents mass-production. According to the technique recently disclosed, the manufacturing process tends to be studied, divided into steps such as purity increase of metallic silicon or solidification technique, which is presumed to be influenced by the above-described manufacturing method.
For example, Japanese Published Unexamined Patent Application No. HEI 5-139713 discloses a process in which silicon having a Iow boron content is obtained by maintaining molten silicon in a container composed of silica or composed mainly of silica, and injecting a plasma gas jet flow of an inert gas to the surface of the molten silicon, while blowing an inert gas upwardly from the bottom of the container.
Japanese Published Unexamined Patent Application No.
HEI 7-17704 discloses a process permitting the efficient removal of boron by forming I.5 to I5 kg of Si02 per kg silicon in advance on the surface of metallic silicon powders upon melting metallic Silicon through an electron beam.
Concerning solidification technique, Japanese Published Unexamined Patent Application No. SHO 61-141612 proposes a technique to prevent, upon casting molten silicon into a mold, precipitation of inclusion in a silicon ingot by turning the mold. In addition, the present applicants themselves are now proposing a method for purifying molten metallic silicon by directional solidification in Japanese Patent Application HEI 7-29500 (filed on February 17, 1995).
It is impossible to say that there does not exist a technique to manufacture solar cell silicon directly from metallic silicon. For example, Japanese Published Unexamined Patent Application No. SHO 62-252393 discloses a process in which a starting material silicon, which is once used as a semiconductor but disposed as an electron industry waste, is subjected to zone melting by plasma jet generated by a mixed gas of argon, hydrogen and oxygen. This process aims principally at the use of an industrial waste so that it does not become a mainly-employed technique suited for mass production of a silicon wafer. In addition, although silicon is used as a raw material, its purity has been once increased so that the process is only a variation of the above-described cumbersome manufacturing process. Japanese Published Unexamined Patent Application No. SHO 63-218506 discloses a process for manufacturing, by plasma melting, silicon in the mass form for solar cells or electronics from metallic silicon in the farm of powders, granules or polished dusts. This method is based on the principle of the zone melting method using the same plasma as that disclosed in the above Japanese Published Unexamined Patent Application No. SHO 62-252393 and is accompanied with the drawback that mass production cannot be carried out in spite of large electricity consumption. According to Examples of the above official gazette, only a silicon rod of 50 g or so is obtained on a laboratory scale and it does not include a description of increasing the size of the silicon wafer for a solar cell to a practical size.
SUMMARY OF THE INVENTION
With the forgoing in view, an object of the present invention is to provide a process and apparatus for mass-producing, at a low cost in continuous flow production, polycrystalline silicon by using metallic silicon or silicon oxide as a starting raw material, and a wafer manufactured using it.
With a view to attaining the above object, the inventors of the present invention have carried out an extensive investigation, paying attention to obtaining the maximum economic effects without using a chemical process but only a metallurgical process, leading to the completion of the present invention.
In a first aspect of the present invention, there is thus provided a process for manufacturing polycrystalline silicon from metallic silicon, which comprises the following steps:
A: melting metallic silicon under vacuum to remove the phosphorus contained therein by evaporation, and then carrying out solidification of the residue for the removal of the impurity elements from the molten silicon (which may hereinafter be called "melt"), thereby obtaining a first ingot;
B: removing the impurity concentrated portion of the first ingot by cutting;
C: re-melting the remaining portion, removing boron and carbon from the melt by oxidizing under an oxidizing atmosphere, and in succession, blowing an argon gas or a mixed gas of argon and hydrogen into the melt for deoxidization.
D: casting the deoxidized melt in a mold, followed by directional solidification to obtain a second ingot; and E: removing the impurity concentrated portion of the second ingot by cutting.
In a further aspect of the present invention, there is also provided a process for the preparation of polycrystalline silicon, wherein in the above-described process, said metallic silicon is obtained by reductive smelting of silicon oxide.
In a still further aspect of the present invention, there is also provided a process for the preparation of polycrystalline silicon, which comprises transferring said metallic silicon under molten state, which has been obtained by smelting of silicon oxide in the above-described process, into a crucible, removing boron and carbon from it by oxidizing under an oxidizing atmosphere, and carrying out solidification, followed by the above-described step B, melting under vacuum and the above-described steps C, D and E.
In a still further aspect of the present invention, there is also provided a process for the preparation of polycrystalline silicon, which comprises forming the z above-described oxidizing atmosphere from an HZO, COZ or Oz gas in an amount small enough so that the whole interface between the melt and the gas will not be covered with silicon oxide, removing silicon oxide formed on the surface of the melt by locally heating by plasma arc, or blowing an H20, COz or Oz gas into the melt instead of placing the melt under the above-described oxidizing atmosphere.
In a still further aspect of the present invention, there is also provided a process for the preparation of polycrystalline silicon, which comprises using Si02 or Si3N4 as a mold releasing agent, setting a solidification interface moving rate at 5 mm/min or less, said solidification being carried out for the removal of impurities, setting a solidification interface moving rate at 2 mm/min or less for directional solidification, or cutting the ingot at a height at least 70o above the bottom of the ingot.
In a still further aspect of the present invention, there is also provided a process for the preparation of polycrystalline silicon which comprises setting a phosphorus concentration of the melt at 0.3 ppm or less and a boron concentration at 0.6 ppm or less or a carbon concentration at 10 ppm or less.
The present invention also relates to an apparatus for manufacturing polycrystalline silicon. In a still further aspect of the present invention, there is also provided an apparatus for manufacturing polycrystalline silicon, which comprises heating means for melting or heating metallic silicon, a retaining container for retaining molten metallic silicon, a first mold in which the melt is cast from the retaining container, a vacuum chamber for removing phosphorus by evaporation, said chamber surrounding the retaining container arid the f first mold, means for removing an impurity concentrated portion of an ingot from the first mold, re-melting mean~o for re-melting or heating a portion of said ingot from the first mold containing fewer impurities, a smelting container for retaining the re-melt 11) a nozzle for blowing or spraying an oxidizing gas, hydrogen gas or a mixed gas of hydrogen and argon to the re-melt in the smelting container and a second. mold for forming the deoxidized re-melt into a cast ingot.
In a still further aspect of the present invention, there is also provided an apparatus for manufacturing polycrystalline silicon, wherein the degree of vacuum :in the above-described vacuum chamber is set at 10-3 torr or higher, the retaining container is a water-cooling jacket made of copper o:r a graphite crucible; and the 2(t smelting container is a crucible made of SiOZ, an SiOz stamped crucible or an Si02 lined crucible.
In a still further aspect of the present invention, there is also provided an apparatus for manufacturing polycrystalline, wherein the above-described heating mE:ans is an electron gun; or the above-described re-melting means is a plasma torch or a DC arc source.
In a still further aspect of the present invention, there is also provided an apparatus for the preparation of polycrystalline silicon, wherein the above-described first and second molds have side walls formed of a heat insulating material and have a bottom formed of a water cooling jacket;
and a heating source for heating the cast melt is disposed above the molds; or a W/H ratio, that is, the ratio of the diameter W to the height H of said mold is set at greater than 0.5.
In a still further and essential aspect of the present invention, there is thus provided a process for the manufacture of a silicon wafer for a solar cell, which comprises slicing an ingot of polycrystalline silicon, which has been obtained by any one of the above-described processes, to a thickness of 100 to 450 a m.
According to the present invention, polycrystalline silicon or a silicon wafer for a solar cell is manufactured by any one of the above-described methods or apparatuses so that the component adjustment of high-purity silicon, which is indispensable in the conventional method, is not required. The present invention also makes it possible to reduce the unnecessary consumption of energy. Since not a chemical process which is characterized by the generation of a large amount of pollutants but only a metallurgical process is adopted, the present invention makes it possible to enlarge the production equipment. As a result, a silicon wafer for a solar cell having excellent photoelectric transfer efficiency can be provided at a cost by far lower t s t than the conventional one. Furthermore, polycrystalline silicon obtained by the enforcement of the present invention can be used effectively not only for the manufacture of a wafer but also for the use as a raw material for iron manufacture or the like.
As described above, the present invention makes it possible to avoid the consumption of unnecessary energy and enlarge the manufacturing equipment, thereby mass-producing polycrystalline silicon or polysilicon wafer for a solar cell having relatively good purity. As a result, a polycrystalline silicon wafer for a solar cell which has a photoelectric transfer efficiency on the ground on the same level with that obtained in the conventional method can be obtained at a markedly low cost, from which the wide diffusion of solar cells are much expected. Polycrystalline silicon can be used effectively as a raw material for iron manufacture as well as that for a wafer.
According to the present invention, high-purity polycrystalline silicon and a silicon wafer for a solar cell can be manufactured through a continuous flow production based on only a metallurgical process. Accordingly, the equipment can be enlarged freely and unnecessary energy can be omitted. The present invention is therefore very useful for the manufacture of a silicon wafer for a solar cell.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a flow chart illustrating one embodiment of a manufacturing process of polycrystalline silicon and a silicon wafer for a solar cell according to the present invention;
FIG. 2 is a flow chart illustrating another embodiment of the manufacturing process of polycrystalline silicon and a silicon wafer for a solar cell according to the present invention;
FIG. 3 is a schematic view illustrating an apparatus embodying the manufacturing process of polycrystalline silicon and a silicon wafer for a solar cell according to the present invention;
FIG. 4 illustrates another apparatus embodying the manufacturing process of polycrystalline silicon and a silicon wafer for a solar cell according to the present invention; and FIG. 5 is a flow chart illustrating the conventional process for manufacturing a silicon wafer for a solar cell.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
In FIG. 1, one embodiment of the manufacturing process of polycrystalline silicon and a silicon wafer for a solar cell according to the present invention is shown together in one flow chart (manufacture of the wafer is shown, enclosed with a dotted line).
First, metallic silicon having a relatively low purity (99.5 wt.o Si) is charged in a retaining container made of graphite or a water-cooling retaining container made of copper and then melted under vacuum. At this time, heating may be conducted making use of the methods known to date such as gas heating or electric heating, with heating by an electron gun being most preferred. Here, the metallic silicon so melted is maintained for a predetermined time (for example, 30 to 60 minutes) in the above retaining container at a temperature not lower than 1450° C but not higher than 1900° C, whereby phosphorus and aluminum, among impurity elements contained in the melt, are removed by evaporation (vacuum smelting). It is preferred that the phosphorus concentration in the melt is 0.3 ppm or less.
Then, in order to remove the impurity elements such as Fe, Al, Ti and Ca to be 100 ppm or less, the melt is cast into a first cast and is cooled upwardly from the bottom so that the moving rate of solidification interface will be 5 mm/min. As a result, an ingot in which the melt having concentrated impurity elements has been solidified last is obtained.
In succession, the upper 30% portion of the ingot having the concentrated impurity elements therein is removed by cutting. The remaining portion of the ingot is charged in a melt furnace equipped with, for example, a plasma arc, whereby the ingot is re-melted. Also in this case, the heating means is not limited to the plasma arc. The melt is heated to a temperature not lower than 1450 ° C and at the same time is reacted with an oxidizing gas atmosphere, whereby boron and carbon are removed from the melt as oxides (oxidative smelting). After oxidative smelting, an argon gas or a mixed gas of argon and hydrogen is blown into the melt for a predetermined time. As a result, oxygen in the melt is deoxidized to the level not higher than 10 ppm. Incidentally, the above-described oxidative smelting may be carried out either in a vacuum chamber or in the air. The deoxidized melt is then cast into a second mold coated with a mold releasing agent, followed by directional solidification, whereby a final ingot is obtained. Impurity elements exist in the concentrated form in the upper portion of the ingot so that the portion (generally, 20% or so) is removed by cutting and the remaining portion is provided as a product of polycrystalline silicon.
Polycrystalline silicon is prepared as described above.
It is only necessary to slice the above-described remaining portion by a multi-wire saw into thin plates of 100 to 450 ~ m thickness.
Metallic silicon, which is a starting material, is generally available by reductive smelting of silicon oxide so that the use of silicon oxide as a starting material is also added to the present invention. Any known methods can be employed to smelt silicon oxide into that having a purity on the same level with that of the metallic silicon used in the first step of the present invention. For example, silicon oxide is melted and reduced by using a carboneous material as a reducing agent. In the present invention, considered is a method of removing the components, which are not necessary for polycrystalline silicon or a silicon wafer for a solar cell, in advance upon obtaining metallic silicon from silicon oxide. It is a method as shown in the flow chart of FIG. 2, wherein metallic silicon which has been obtained from silicon oxide, has a relatively low purity and is under molten state is charged in a smelting container (for example, crucible) and so-called preliminary smelting is effected. Described specifically, an oxidizing gas (H20, COz or the like) is blown into the melt in the crucible, boron and carbon are removed as oxides and then, the residue is solidified. The ingot so obtained is melted in the above-described vacuum chamber, phosphorus is removed from the melt by vacuum smelting and the residue is subjected to directional solidification, whereby an ingot of polycrystalline silicon is obtained. It is only necessary to slice the ingot into thin plates as described above to obtain a wafer. This process has a merit in that the above-described steps of "boron and carbon removal" and "solidification for the removal of impurities" of the present invention can be omitted by changing a part of ordinary metallic silicon preparation operations. As a result, this process makes it possible to omit some of the apparatuses and brings about ' CA 02211028 1997-08-04 effects for reducing energy consumption, whereby polycrystalline silicon and a silicon wafer for a solar cell on the same level with those obtained by the above-described process of the present invention are available at a lower cost. In particular, if boron and carbon removal is conducted by those who prepare metallic silicon, operations subsequent to it can be carried out more easily by the manufacturer of polycrystalline silicon or wafer.
Incidentally, the reason for setting the moving rate of the solidification interface at 5 mm/min or lower in the case of the first mold and at 2 mm/min in the case of the second mold is because moving rates higher than the above disturb sufficient concentration of impurity metal elements in the upper part of the ingot. The reason for cutting the ingot at a height not lower than 70% from the bottom of the ingot is because the target composition as polycrystalline silicon can be attained at the remaining lower portion. In the present invention, the degree of vacuum in the vacuum chamber is set at 10-3 torr or higher because it is suited for phosphorus removal by evaporation judging from the vapor pressure of phosphorus in metallic silicon.
In the present invention, the phosphorus concentration of the melt is set at 0.3 ppm or lower in order to secure stable operation of solar cells, while the boron concentration of the melt is set at 0.6 ppm or lower in order to obtain polycrystalline silicon suited for a P-type semiconductor wafer. The carbon concentration set at 10 ppm or lower makes it possible to suppress the precipitation of SiC in silicon crystals, thereby preventing the lowering in the photoelectric transfer efficiency.
Furthermore, in the present invention, a copper-made water-cooling jacket or a graphite crucible is employed as the above-described retaining container upon melting of metallic silicon and an Si02 crucible or Si02 stamped or lined crucible is used as the above-described smelting container, because silicon tends to react with other substances and when a crucible made of another substance is used, component elements of the substance is mixed in silicon. Incidentally, when boron is removed upon preparation of metallic silicon, inexpensive A1203, MgO, graphite or the like can be employed for the lining of the refractory, because if impurities are mixed in, they can be removed at the subsequent step. The mold releasing agent of the mold used for solidification is specified to SiOz or Si3N4 because of the same reason. Since the molten silicon expands by 10%
in volume when solidified, the mold releasing agent is necessary for preventing the stress from remaining on the ingot.
In addition, an apparatus according to the present invention is constructed so that as shown in FIG. 3, the melt 2 of metallic silicon 1 flows to the subsequent stage almost continuously except at the time of solidification. This structure makes it possible to carry out preparation smoothly and to shorten the operation time, leading to the reduction in the manufacturing cost. Besides, since the apparatuses used in the present invention are operated based on only the metallurgical process, they can be enlarged considerably and are free from generation of pollutants. Cost reduction by mass production can also be expected.
The oxidizing atmosphere for the removal of boron and carbon from the melt 2 is not required to have high acidifying power. Preferred as the oxidizing gas is H20 or CO2. When acidifying power is high, an Si02 film is formed on the surface of the melt, which hinders the removal of boron and COZ. In such a case, injection of arc from a plasma torch 4 or DC arc source is necessary for the removal of such a film. The above-described oxidizing gas may be blown directly into the melt. The material of a nozzle 5 from which the oxidizing gas is blown is limited to graphite or SiOz, because other materials contaminate the melt 2.
Incidentally, as a cutting machine (not illustrated) for cutting the ingot 6 released from the second mold 9 into thin plates, a known multi-wire saw or multi-blade saw can be used without problems. The reason why the thickness of the thin plate is set at 100 to 450 ~c m is because the plate is too weak at the thickness less than 100 ~c m, while it has lowered photoelectric transfer efficiency at the thickness exceeding 450 ~ m.
a In the apparatus according to the present invention, a particular consideration is taken for the structure of the mold 9 in which solidification is carried out. Described specifically, as shown in FIG. 3, the mold is shaped into a so-called washball having a diameter W . height H ratio of 0.5 or greater. In addition, it is constructed to have a heat insulating material 11 as a side wall, a water-cooled jacket 10 as a bottom and a heating source 8 disposed in the upper part of the mold so that the moving rate of the solidification interface can be regulated.
In the present invention, it is also possible to carry out the solidification operations (solidification - re-melting) in the first mold and second mold in repetition.
Alternatively, after a plurality of molds are provided and the above-described retaining container or smelting container is enlarged, the melt may be poured from the enlarged container in portions to the plural molds. Moreover, it is not necessary to effect the steps A, B, C, D and E in this order except that the steps D and E come last.
(Example 1) As shown in FIG. 3, an electron gun 3 of 300 KW in output was installed on the upper part of a vacuum chamber 18.
Metallic silicon 1 was fed to a retaining container 19 (which is also called a melting furnace) made of graphite at kg/hour and was melted. At this time, the degree of vacuum in the vacuum chamber 18 was 10-5 torr. From the melt 2, a portion of phosphorus and aluminum elements were evaporated and removed. The remaining melt 2 was then cast into a water-cooling type copper-made mold 9. While the surface of the melt was exposed to electron beam 3 to maintain the molten state, the melt was solidified from the bottom at a solidification interface moving rate of 1 mm/min, whereby 50 kg of an ingot 6 were obtained. The upper 20%
portion of the ingot 6 (the portion A) was removed by cutting to obtain an ingot having a chemical composition as shown in Table 1.
Table 1 ( Unit:ppm ) B P Fe A1 Ti La C O
Metallic 7 23 980 860 180 950 ~-5000 -silicon Ingot after crude 7 <0.1 10 8.5 2 10 35 -purification Wafer 0.1 <0.1 <0.1 <0.1 <0.1 <0.1 3.5 5.7 The remaining portion of the ingot 6 was then melted in a silica crucible (smelting container) I6 above which a plasma torch 4 of 100 KW in output was disposed. The melt was kept at a temperature of 1600 ° C and a mixed gas 2I of argon and water vapor, said gas containing 15 vol.~ of water vapor, was sprayed to the surface of the melt. At this time, a sample was taken from the melt Z and its specific resistivity was measured. About two hours later, the specific resistivity became I ohm~ cm so that the mixed gas 21 was changed to an argon gas and deoxidization was effected for 30 minutes. The melt was then poured into a second mold which was made of graphite and coated with Si3NQ as a mold release agent and was solidified by cooling upwardly from the bottom under an argon gas atmosphere, whereby an ingot was obtained. At this time, a graphite heater $ was disposed in the upper part of the mold 9 by which the surface of the melt was heated. As a result, the moving rate of the solidification interface was 0.7 mm/min.
After the completion of the solidification, the upper 30% of the ingot 6 so obtained was removed by cutting and the remaining portion of the ingot was provided as a product of polycrystalline silicon. The product so obtained was sliced into thin plates having a thickness of 350 ~ m, by a mufti-wire saw, whereby 300 silicon wafers for solar cells, each wafer having a size of 15 cm x I5 cm, were manufactured. These wafers each had a specific resistivity of 1.2 ohm~cm, had a minority carrier whose life time was 12 sec and, had a photoelectric transfer efficiency of 13.8%.
Its chemical composition is as shown in Table 1.
(Example 2) In a similar manner to Example 1, an ingot 6 was obtained from the first mold. The upper 70% portion of the ingot was melted in a silica crucible (smelting container) 16 above which a plasma torch 4 of 100 KW in output was disposed. Into the melt 2 maintained at 1600 ° C, a mixed gas 21 of argon and water vapor, said gas containing 15 vol.o of water vapor, was blown at a rate of 10 liter/min through a porous plug 15 disposed at the bottom of the crucible 16, whereby boron and carbon were removed from the melt. The residue was subjected to deoxidization, directional solidification and removal by cutting, whereby a product of polycrystalline silicon was obtained. The product was sliced in a similar manner to Example 1, whereby silicon wafers for solar cells were manufactured.
The size, number and performance of the wafer so obtained were much the same with those of the wafer obtained in Example 1.
(Example 3) Using silicon oxide as a starting material, an arc electric furnace 12 as shown in FIG. 4 and a carbonaceous reducing agent, melting and reduction were carried out, whereby molten metallic silicon having a chemical composition as shown in Table 2 was manufacture. In a crucible 14 equipped with a porous plug 15 at the bottom thereof and lined with a siliceous refractory, 50 kg of the metallic silicon 1 were charged. Then, a mixed gas of argon and water vapor, said gas containing 20 vol% of water vapor, was blown into the melt for 30 minutes through the porous plug 15. The remaining melt 2 was heated to 1650 ° C by the oxidizing heat of silicon and boron- and carbon-removal reaction occurred. The melt 2 was cast into a first mold which had an SiC-made heater disposed in the upper part of the mold and had a bottom cooling system, and was solidified by cooling at a moving rate of the solidification surface at 1.5 mm/min. The lower 80o portion of the ingot so obtained was melted in succession in the retaining container disposed in the above-described vacuum chamber, followed by dephosphorization and deoxidization. The resulting melt was poured into the second mold, whereby directional solidification was effected. The upper 30o portion of the ingot 6 so obtained was removed by cutting and the remaining portion was provided as a product of polycrystalline silicon. The product was sliced by a multi-blade saw into thin plates of the above size, whereby 300 polycrystalline silicon wafers for solar cells were obtained. The wafers each had a specific resistivity of 0.9 ohm cm, had a minority carrier whose life time was 10 ~ sec and had a photoelectric transfer efficiency of 13.5%. It had a chemical composition as shown in Table 2.
Table 2 ( Unit . ppm ) H P Fe A1 Ti Ca C O
Metallic 7 25 1010 800 180 950 ~-5000 -silicon Ingot after 7 23 10 25 3 13 6 40 smelting in crucible Wafer 0.I <0.1 <0.1 <0.1 <0.1 <0.1 4 1 In conclusion, the advantages of the manufacturing process and apparatus of polycrystalline silicon and manufacturing process of polycrystalline silicon wafers for solar cells according to the present invention will be summarized below compared with the conventional ones.
The processes for manufacturing polycrystalline silicon and polycrystalline silicon wafers for solar cells according to the present invention are free from the source-wise problem (in other words, shortage in raw materials does not occur), do not by-produce pollutants and are essentially suited to the scale up of the equipment and mass production because of a metallurgical technique employed. It is therefore possible to supply wafers stabiy even if the demand for solar cells will increase by several hundred times ' CA 02211028 1997-08-04 in future. In addition, during the manufacture of wafers from high-purity silicon in the mass form, about 20 wt.% of losses and inferior products appear as a result of pulverization or the like. Continuous and consistent manufacture from silicon to wafers according to the present invention, on the other hand, reduces losses, whereby electricity and energy can be used effectively. The price of the silicon wafer available in the enforcement of the present invention can be reduced to half of that of the conventional product, which makes it possible to allow the solar cell to function economically as an electricity generating apparatus.
Recently, those having a photoelectric transfer efficiency of even about 13 to 15% under sun light on the ground have appeared and they are now being industrialized for various applications. In our country, however, solar cells are not so popular as an energy source for domestic electric power, automobiles, ships or machine tools, because a technique to mass-produce a silicon wafer at a low cost, which is necessary for the manufacture of solar cells, has not yet been established.
At present, for the manufacture of a silicon wafer for a solar cell, a high-purity silicon, which is in the mass form and conforms to the specification of a semiconductor, is once manufactured through a chemical process by using as a starting material a low purity metallic silicon (99.5 wt.%
Si). Then, high-purity silicon in the mass form is re-melted and is adjusted to have a chemical composition suited to a solar cell by a metallurgical process. The resulting molten silicon is formed into an ingot by the pulling method or directional solidification method, followed by slicing into thin plates. Described specifically, as shown in FIG S, metallic silicon is first reacted with hydrochloric acid and formed into a trichlorosilane gas. After the gas so obtained is fractionated to remove the impurity elements, the residue is reacted with a hydrogen gas, whereby high-purity silicon is precipitated from the gas by the so-called CVD
(Chemical Vapor Deposition) method. The high-purity silicon therefore becomes only an aggregate of silicon grains owing to the weak bonding power between crystal grains. The boron contained in the high-purity silicon forming the aggregate is reduced even in the order of O.OOI ppm and does not reach the concentration necessary for satisfying the specific resistivity of 0.5 to I.5 ohm~cm which is the specification for P-type semiconductor wafer. In order to use the above high-purity silicon for a solar cell, it is indispensable to adjust the specific resistivity and to control the crystallinity of single crystals or crystal grains so as to . CA 02211028 1997-08-04 have a particle size not smaller than several mm and have a grain boundary so as not to exert adverse effects on the photoelectric transfer efficiency. The above silicon cannot be formed into a wafer without further treatment. As shown in the right hand of FIG. 5, it becomes necessary to form a wafer after re-melting the high-purity silicon mass, adjusting the components of the melt (by the addition of boron) and forming into an ingot (pulling method for single crystals, while directional solidification for polycrystals).
The above-described manufacturing method is however accompanied with the drawbacks that it requires much labor to re-adjust (mainly, by the addition of boron) the components of a silicon ingot, which has a purity intentionally heightened to be suitable for semiconductor, to be suitable for solar cells or to purify the ingot; its yield is inferior; it additionally requires equipment and energy for re-melting; and therefore it costs high. As described above, the solar cells available now are therefore expensive, which prevents them from being popularly used. The purity heightening of metallic silicon by a chemical process is also accompanied with the generation of a large amount of pollutants such as silane and chloride, which prevents mass-production. According to the technique recently disclosed, the manufacturing process tends to be studied, divided into steps such as purity increase of metallic silicon or solidification technique, which is presumed to be influenced by the above-described manufacturing method.
For example, Japanese Published Unexamined Patent Application No. HEI 5-139713 discloses a process in which silicon having a Iow boron content is obtained by maintaining molten silicon in a container composed of silica or composed mainly of silica, and injecting a plasma gas jet flow of an inert gas to the surface of the molten silicon, while blowing an inert gas upwardly from the bottom of the container.
Japanese Published Unexamined Patent Application No.
HEI 7-17704 discloses a process permitting the efficient removal of boron by forming I.5 to I5 kg of Si02 per kg silicon in advance on the surface of metallic silicon powders upon melting metallic Silicon through an electron beam.
Concerning solidification technique, Japanese Published Unexamined Patent Application No. SHO 61-141612 proposes a technique to prevent, upon casting molten silicon into a mold, precipitation of inclusion in a silicon ingot by turning the mold. In addition, the present applicants themselves are now proposing a method for purifying molten metallic silicon by directional solidification in Japanese Patent Application HEI 7-29500 (filed on February 17, 1995).
It is impossible to say that there does not exist a technique to manufacture solar cell silicon directly from metallic silicon. For example, Japanese Published Unexamined Patent Application No. SHO 62-252393 discloses a process in which a starting material silicon, which is once used as a semiconductor but disposed as an electron industry waste, is subjected to zone melting by plasma jet generated by a mixed gas of argon, hydrogen and oxygen. This process aims principally at the use of an industrial waste so that it does not become a mainly-employed technique suited for mass production of a silicon wafer. In addition, although silicon is used as a raw material, its purity has been once increased so that the process is only a variation of the above-described cumbersome manufacturing process. Japanese Published Unexamined Patent Application No. SHO 63-218506 discloses a process for manufacturing, by plasma melting, silicon in the mass form for solar cells or electronics from metallic silicon in the farm of powders, granules or polished dusts. This method is based on the principle of the zone melting method using the same plasma as that disclosed in the above Japanese Published Unexamined Patent Application No. SHO 62-252393 and is accompanied with the drawback that mass production cannot be carried out in spite of large electricity consumption. According to Examples of the above official gazette, only a silicon rod of 50 g or so is obtained on a laboratory scale and it does not include a description of increasing the size of the silicon wafer for a solar cell to a practical size.
SUMMARY OF THE INVENTION
With the forgoing in view, an object of the present invention is to provide a process and apparatus for mass-producing, at a low cost in continuous flow production, polycrystalline silicon by using metallic silicon or silicon oxide as a starting raw material, and a wafer manufactured using it.
With a view to attaining the above object, the inventors of the present invention have carried out an extensive investigation, paying attention to obtaining the maximum economic effects without using a chemical process but only a metallurgical process, leading to the completion of the present invention.
In a first aspect of the present invention, there is thus provided a process for manufacturing polycrystalline silicon from metallic silicon, which comprises the following steps:
A: melting metallic silicon under vacuum to remove the phosphorus contained therein by evaporation, and then carrying out solidification of the residue for the removal of the impurity elements from the molten silicon (which may hereinafter be called "melt"), thereby obtaining a first ingot;
B: removing the impurity concentrated portion of the first ingot by cutting;
C: re-melting the remaining portion, removing boron and carbon from the melt by oxidizing under an oxidizing atmosphere, and in succession, blowing an argon gas or a mixed gas of argon and hydrogen into the melt for deoxidization.
D: casting the deoxidized melt in a mold, followed by directional solidification to obtain a second ingot; and E: removing the impurity concentrated portion of the second ingot by cutting.
In a further aspect of the present invention, there is also provided a process for the preparation of polycrystalline silicon, wherein in the above-described process, said metallic silicon is obtained by reductive smelting of silicon oxide.
In a still further aspect of the present invention, there is also provided a process for the preparation of polycrystalline silicon, which comprises transferring said metallic silicon under molten state, which has been obtained by smelting of silicon oxide in the above-described process, into a crucible, removing boron and carbon from it by oxidizing under an oxidizing atmosphere, and carrying out solidification, followed by the above-described step B, melting under vacuum and the above-described steps C, D and E.
In a still further aspect of the present invention, there is also provided a process for the preparation of polycrystalline silicon, which comprises forming the z above-described oxidizing atmosphere from an HZO, COZ or Oz gas in an amount small enough so that the whole interface between the melt and the gas will not be covered with silicon oxide, removing silicon oxide formed on the surface of the melt by locally heating by plasma arc, or blowing an H20, COz or Oz gas into the melt instead of placing the melt under the above-described oxidizing atmosphere.
In a still further aspect of the present invention, there is also provided a process for the preparation of polycrystalline silicon, which comprises using Si02 or Si3N4 as a mold releasing agent, setting a solidification interface moving rate at 5 mm/min or less, said solidification being carried out for the removal of impurities, setting a solidification interface moving rate at 2 mm/min or less for directional solidification, or cutting the ingot at a height at least 70o above the bottom of the ingot.
In a still further aspect of the present invention, there is also provided a process for the preparation of polycrystalline silicon which comprises setting a phosphorus concentration of the melt at 0.3 ppm or less and a boron concentration at 0.6 ppm or less or a carbon concentration at 10 ppm or less.
The present invention also relates to an apparatus for manufacturing polycrystalline silicon. In a still further aspect of the present invention, there is also provided an apparatus for manufacturing polycrystalline silicon, which comprises heating means for melting or heating metallic silicon, a retaining container for retaining molten metallic silicon, a first mold in which the melt is cast from the retaining container, a vacuum chamber for removing phosphorus by evaporation, said chamber surrounding the retaining container arid the f first mold, means for removing an impurity concentrated portion of an ingot from the first mold, re-melting mean~o for re-melting or heating a portion of said ingot from the first mold containing fewer impurities, a smelting container for retaining the re-melt 11) a nozzle for blowing or spraying an oxidizing gas, hydrogen gas or a mixed gas of hydrogen and argon to the re-melt in the smelting container and a second. mold for forming the deoxidized re-melt into a cast ingot.
In a still further aspect of the present invention, there is also provided an apparatus for manufacturing polycrystalline silicon, wherein the degree of vacuum :in the above-described vacuum chamber is set at 10-3 torr or higher, the retaining container is a water-cooling jacket made of copper o:r a graphite crucible; and the 2(t smelting container is a crucible made of SiOZ, an SiOz stamped crucible or an Si02 lined crucible.
In a still further aspect of the present invention, there is also provided an apparatus for manufacturing polycrystalline, wherein the above-described heating mE:ans is an electron gun; or the above-described re-melting means is a plasma torch or a DC arc source.
In a still further aspect of the present invention, there is also provided an apparatus for the preparation of polycrystalline silicon, wherein the above-described first and second molds have side walls formed of a heat insulating material and have a bottom formed of a water cooling jacket;
and a heating source for heating the cast melt is disposed above the molds; or a W/H ratio, that is, the ratio of the diameter W to the height H of said mold is set at greater than 0.5.
In a still further and essential aspect of the present invention, there is thus provided a process for the manufacture of a silicon wafer for a solar cell, which comprises slicing an ingot of polycrystalline silicon, which has been obtained by any one of the above-described processes, to a thickness of 100 to 450 a m.
According to the present invention, polycrystalline silicon or a silicon wafer for a solar cell is manufactured by any one of the above-described methods or apparatuses so that the component adjustment of high-purity silicon, which is indispensable in the conventional method, is not required. The present invention also makes it possible to reduce the unnecessary consumption of energy. Since not a chemical process which is characterized by the generation of a large amount of pollutants but only a metallurgical process is adopted, the present invention makes it possible to enlarge the production equipment. As a result, a silicon wafer for a solar cell having excellent photoelectric transfer efficiency can be provided at a cost by far lower t s t than the conventional one. Furthermore, polycrystalline silicon obtained by the enforcement of the present invention can be used effectively not only for the manufacture of a wafer but also for the use as a raw material for iron manufacture or the like.
As described above, the present invention makes it possible to avoid the consumption of unnecessary energy and enlarge the manufacturing equipment, thereby mass-producing polycrystalline silicon or polysilicon wafer for a solar cell having relatively good purity. As a result, a polycrystalline silicon wafer for a solar cell which has a photoelectric transfer efficiency on the ground on the same level with that obtained in the conventional method can be obtained at a markedly low cost, from which the wide diffusion of solar cells are much expected. Polycrystalline silicon can be used effectively as a raw material for iron manufacture as well as that for a wafer.
According to the present invention, high-purity polycrystalline silicon and a silicon wafer for a solar cell can be manufactured through a continuous flow production based on only a metallurgical process. Accordingly, the equipment can be enlarged freely and unnecessary energy can be omitted. The present invention is therefore very useful for the manufacture of a silicon wafer for a solar cell.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a flow chart illustrating one embodiment of a manufacturing process of polycrystalline silicon and a silicon wafer for a solar cell according to the present invention;
FIG. 2 is a flow chart illustrating another embodiment of the manufacturing process of polycrystalline silicon and a silicon wafer for a solar cell according to the present invention;
FIG. 3 is a schematic view illustrating an apparatus embodying the manufacturing process of polycrystalline silicon and a silicon wafer for a solar cell according to the present invention;
FIG. 4 illustrates another apparatus embodying the manufacturing process of polycrystalline silicon and a silicon wafer for a solar cell according to the present invention; and FIG. 5 is a flow chart illustrating the conventional process for manufacturing a silicon wafer for a solar cell.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
In FIG. 1, one embodiment of the manufacturing process of polycrystalline silicon and a silicon wafer for a solar cell according to the present invention is shown together in one flow chart (manufacture of the wafer is shown, enclosed with a dotted line).
First, metallic silicon having a relatively low purity (99.5 wt.o Si) is charged in a retaining container made of graphite or a water-cooling retaining container made of copper and then melted under vacuum. At this time, heating may be conducted making use of the methods known to date such as gas heating or electric heating, with heating by an electron gun being most preferred. Here, the metallic silicon so melted is maintained for a predetermined time (for example, 30 to 60 minutes) in the above retaining container at a temperature not lower than 1450° C but not higher than 1900° C, whereby phosphorus and aluminum, among impurity elements contained in the melt, are removed by evaporation (vacuum smelting). It is preferred that the phosphorus concentration in the melt is 0.3 ppm or less.
Then, in order to remove the impurity elements such as Fe, Al, Ti and Ca to be 100 ppm or less, the melt is cast into a first cast and is cooled upwardly from the bottom so that the moving rate of solidification interface will be 5 mm/min. As a result, an ingot in which the melt having concentrated impurity elements has been solidified last is obtained.
In succession, the upper 30% portion of the ingot having the concentrated impurity elements therein is removed by cutting. The remaining portion of the ingot is charged in a melt furnace equipped with, for example, a plasma arc, whereby the ingot is re-melted. Also in this case, the heating means is not limited to the plasma arc. The melt is heated to a temperature not lower than 1450 ° C and at the same time is reacted with an oxidizing gas atmosphere, whereby boron and carbon are removed from the melt as oxides (oxidative smelting). After oxidative smelting, an argon gas or a mixed gas of argon and hydrogen is blown into the melt for a predetermined time. As a result, oxygen in the melt is deoxidized to the level not higher than 10 ppm. Incidentally, the above-described oxidative smelting may be carried out either in a vacuum chamber or in the air. The deoxidized melt is then cast into a second mold coated with a mold releasing agent, followed by directional solidification, whereby a final ingot is obtained. Impurity elements exist in the concentrated form in the upper portion of the ingot so that the portion (generally, 20% or so) is removed by cutting and the remaining portion is provided as a product of polycrystalline silicon.
Polycrystalline silicon is prepared as described above.
It is only necessary to slice the above-described remaining portion by a multi-wire saw into thin plates of 100 to 450 ~ m thickness.
Metallic silicon, which is a starting material, is generally available by reductive smelting of silicon oxide so that the use of silicon oxide as a starting material is also added to the present invention. Any known methods can be employed to smelt silicon oxide into that having a purity on the same level with that of the metallic silicon used in the first step of the present invention. For example, silicon oxide is melted and reduced by using a carboneous material as a reducing agent. In the present invention, considered is a method of removing the components, which are not necessary for polycrystalline silicon or a silicon wafer for a solar cell, in advance upon obtaining metallic silicon from silicon oxide. It is a method as shown in the flow chart of FIG. 2, wherein metallic silicon which has been obtained from silicon oxide, has a relatively low purity and is under molten state is charged in a smelting container (for example, crucible) and so-called preliminary smelting is effected. Described specifically, an oxidizing gas (H20, COz or the like) is blown into the melt in the crucible, boron and carbon are removed as oxides and then, the residue is solidified. The ingot so obtained is melted in the above-described vacuum chamber, phosphorus is removed from the melt by vacuum smelting and the residue is subjected to directional solidification, whereby an ingot of polycrystalline silicon is obtained. It is only necessary to slice the ingot into thin plates as described above to obtain a wafer. This process has a merit in that the above-described steps of "boron and carbon removal" and "solidification for the removal of impurities" of the present invention can be omitted by changing a part of ordinary metallic silicon preparation operations. As a result, this process makes it possible to omit some of the apparatuses and brings about ' CA 02211028 1997-08-04 effects for reducing energy consumption, whereby polycrystalline silicon and a silicon wafer for a solar cell on the same level with those obtained by the above-described process of the present invention are available at a lower cost. In particular, if boron and carbon removal is conducted by those who prepare metallic silicon, operations subsequent to it can be carried out more easily by the manufacturer of polycrystalline silicon or wafer.
Incidentally, the reason for setting the moving rate of the solidification interface at 5 mm/min or lower in the case of the first mold and at 2 mm/min in the case of the second mold is because moving rates higher than the above disturb sufficient concentration of impurity metal elements in the upper part of the ingot. The reason for cutting the ingot at a height not lower than 70% from the bottom of the ingot is because the target composition as polycrystalline silicon can be attained at the remaining lower portion. In the present invention, the degree of vacuum in the vacuum chamber is set at 10-3 torr or higher because it is suited for phosphorus removal by evaporation judging from the vapor pressure of phosphorus in metallic silicon.
In the present invention, the phosphorus concentration of the melt is set at 0.3 ppm or lower in order to secure stable operation of solar cells, while the boron concentration of the melt is set at 0.6 ppm or lower in order to obtain polycrystalline silicon suited for a P-type semiconductor wafer. The carbon concentration set at 10 ppm or lower makes it possible to suppress the precipitation of SiC in silicon crystals, thereby preventing the lowering in the photoelectric transfer efficiency.
Furthermore, in the present invention, a copper-made water-cooling jacket or a graphite crucible is employed as the above-described retaining container upon melting of metallic silicon and an Si02 crucible or Si02 stamped or lined crucible is used as the above-described smelting container, because silicon tends to react with other substances and when a crucible made of another substance is used, component elements of the substance is mixed in silicon. Incidentally, when boron is removed upon preparation of metallic silicon, inexpensive A1203, MgO, graphite or the like can be employed for the lining of the refractory, because if impurities are mixed in, they can be removed at the subsequent step. The mold releasing agent of the mold used for solidification is specified to SiOz or Si3N4 because of the same reason. Since the molten silicon expands by 10%
in volume when solidified, the mold releasing agent is necessary for preventing the stress from remaining on the ingot.
In addition, an apparatus according to the present invention is constructed so that as shown in FIG. 3, the melt 2 of metallic silicon 1 flows to the subsequent stage almost continuously except at the time of solidification. This structure makes it possible to carry out preparation smoothly and to shorten the operation time, leading to the reduction in the manufacturing cost. Besides, since the apparatuses used in the present invention are operated based on only the metallurgical process, they can be enlarged considerably and are free from generation of pollutants. Cost reduction by mass production can also be expected.
The oxidizing atmosphere for the removal of boron and carbon from the melt 2 is not required to have high acidifying power. Preferred as the oxidizing gas is H20 or CO2. When acidifying power is high, an Si02 film is formed on the surface of the melt, which hinders the removal of boron and COZ. In such a case, injection of arc from a plasma torch 4 or DC arc source is necessary for the removal of such a film. The above-described oxidizing gas may be blown directly into the melt. The material of a nozzle 5 from which the oxidizing gas is blown is limited to graphite or SiOz, because other materials contaminate the melt 2.
Incidentally, as a cutting machine (not illustrated) for cutting the ingot 6 released from the second mold 9 into thin plates, a known multi-wire saw or multi-blade saw can be used without problems. The reason why the thickness of the thin plate is set at 100 to 450 ~c m is because the plate is too weak at the thickness less than 100 ~c m, while it has lowered photoelectric transfer efficiency at the thickness exceeding 450 ~ m.
a In the apparatus according to the present invention, a particular consideration is taken for the structure of the mold 9 in which solidification is carried out. Described specifically, as shown in FIG. 3, the mold is shaped into a so-called washball having a diameter W . height H ratio of 0.5 or greater. In addition, it is constructed to have a heat insulating material 11 as a side wall, a water-cooled jacket 10 as a bottom and a heating source 8 disposed in the upper part of the mold so that the moving rate of the solidification interface can be regulated.
In the present invention, it is also possible to carry out the solidification operations (solidification - re-melting) in the first mold and second mold in repetition.
Alternatively, after a plurality of molds are provided and the above-described retaining container or smelting container is enlarged, the melt may be poured from the enlarged container in portions to the plural molds. Moreover, it is not necessary to effect the steps A, B, C, D and E in this order except that the steps D and E come last.
(Example 1) As shown in FIG. 3, an electron gun 3 of 300 KW in output was installed on the upper part of a vacuum chamber 18.
Metallic silicon 1 was fed to a retaining container 19 (which is also called a melting furnace) made of graphite at kg/hour and was melted. At this time, the degree of vacuum in the vacuum chamber 18 was 10-5 torr. From the melt 2, a portion of phosphorus and aluminum elements were evaporated and removed. The remaining melt 2 was then cast into a water-cooling type copper-made mold 9. While the surface of the melt was exposed to electron beam 3 to maintain the molten state, the melt was solidified from the bottom at a solidification interface moving rate of 1 mm/min, whereby 50 kg of an ingot 6 were obtained. The upper 20%
portion of the ingot 6 (the portion A) was removed by cutting to obtain an ingot having a chemical composition as shown in Table 1.
Table 1 ( Unit:ppm ) B P Fe A1 Ti La C O
Metallic 7 23 980 860 180 950 ~-5000 -silicon Ingot after crude 7 <0.1 10 8.5 2 10 35 -purification Wafer 0.1 <0.1 <0.1 <0.1 <0.1 <0.1 3.5 5.7 The remaining portion of the ingot 6 was then melted in a silica crucible (smelting container) I6 above which a plasma torch 4 of 100 KW in output was disposed. The melt was kept at a temperature of 1600 ° C and a mixed gas 2I of argon and water vapor, said gas containing 15 vol.~ of water vapor, was sprayed to the surface of the melt. At this time, a sample was taken from the melt Z and its specific resistivity was measured. About two hours later, the specific resistivity became I ohm~ cm so that the mixed gas 21 was changed to an argon gas and deoxidization was effected for 30 minutes. The melt was then poured into a second mold which was made of graphite and coated with Si3NQ as a mold release agent and was solidified by cooling upwardly from the bottom under an argon gas atmosphere, whereby an ingot was obtained. At this time, a graphite heater $ was disposed in the upper part of the mold 9 by which the surface of the melt was heated. As a result, the moving rate of the solidification interface was 0.7 mm/min.
After the completion of the solidification, the upper 30% of the ingot 6 so obtained was removed by cutting and the remaining portion of the ingot was provided as a product of polycrystalline silicon. The product so obtained was sliced into thin plates having a thickness of 350 ~ m, by a mufti-wire saw, whereby 300 silicon wafers for solar cells, each wafer having a size of 15 cm x I5 cm, were manufactured. These wafers each had a specific resistivity of 1.2 ohm~cm, had a minority carrier whose life time was 12 sec and, had a photoelectric transfer efficiency of 13.8%.
Its chemical composition is as shown in Table 1.
(Example 2) In a similar manner to Example 1, an ingot 6 was obtained from the first mold. The upper 70% portion of the ingot was melted in a silica crucible (smelting container) 16 above which a plasma torch 4 of 100 KW in output was disposed. Into the melt 2 maintained at 1600 ° C, a mixed gas 21 of argon and water vapor, said gas containing 15 vol.o of water vapor, was blown at a rate of 10 liter/min through a porous plug 15 disposed at the bottom of the crucible 16, whereby boron and carbon were removed from the melt. The residue was subjected to deoxidization, directional solidification and removal by cutting, whereby a product of polycrystalline silicon was obtained. The product was sliced in a similar manner to Example 1, whereby silicon wafers for solar cells were manufactured.
The size, number and performance of the wafer so obtained were much the same with those of the wafer obtained in Example 1.
(Example 3) Using silicon oxide as a starting material, an arc electric furnace 12 as shown in FIG. 4 and a carbonaceous reducing agent, melting and reduction were carried out, whereby molten metallic silicon having a chemical composition as shown in Table 2 was manufacture. In a crucible 14 equipped with a porous plug 15 at the bottom thereof and lined with a siliceous refractory, 50 kg of the metallic silicon 1 were charged. Then, a mixed gas of argon and water vapor, said gas containing 20 vol% of water vapor, was blown into the melt for 30 minutes through the porous plug 15. The remaining melt 2 was heated to 1650 ° C by the oxidizing heat of silicon and boron- and carbon-removal reaction occurred. The melt 2 was cast into a first mold which had an SiC-made heater disposed in the upper part of the mold and had a bottom cooling system, and was solidified by cooling at a moving rate of the solidification surface at 1.5 mm/min. The lower 80o portion of the ingot so obtained was melted in succession in the retaining container disposed in the above-described vacuum chamber, followed by dephosphorization and deoxidization. The resulting melt was poured into the second mold, whereby directional solidification was effected. The upper 30o portion of the ingot 6 so obtained was removed by cutting and the remaining portion was provided as a product of polycrystalline silicon. The product was sliced by a multi-blade saw into thin plates of the above size, whereby 300 polycrystalline silicon wafers for solar cells were obtained. The wafers each had a specific resistivity of 0.9 ohm cm, had a minority carrier whose life time was 10 ~ sec and had a photoelectric transfer efficiency of 13.5%. It had a chemical composition as shown in Table 2.
Table 2 ( Unit . ppm ) H P Fe A1 Ti Ca C O
Metallic 7 25 1010 800 180 950 ~-5000 -silicon Ingot after 7 23 10 25 3 13 6 40 smelting in crucible Wafer 0.I <0.1 <0.1 <0.1 <0.1 <0.1 4 1 In conclusion, the advantages of the manufacturing process and apparatus of polycrystalline silicon and manufacturing process of polycrystalline silicon wafers for solar cells according to the present invention will be summarized below compared with the conventional ones.
The processes for manufacturing polycrystalline silicon and polycrystalline silicon wafers for solar cells according to the present invention are free from the source-wise problem (in other words, shortage in raw materials does not occur), do not by-produce pollutants and are essentially suited to the scale up of the equipment and mass production because of a metallurgical technique employed. It is therefore possible to supply wafers stabiy even if the demand for solar cells will increase by several hundred times ' CA 02211028 1997-08-04 in future. In addition, during the manufacture of wafers from high-purity silicon in the mass form, about 20 wt.% of losses and inferior products appear as a result of pulverization or the like. Continuous and consistent manufacture from silicon to wafers according to the present invention, on the other hand, reduces losses, whereby electricity and energy can be used effectively. The price of the silicon wafer available in the enforcement of the present invention can be reduced to half of that of the conventional product, which makes it possible to allow the solar cell to function economically as an electricity generating apparatus.
Claims (21)
1. A process for manufacturing polycrystalline silicon from metallic silicon, which comprises the following steps:
A: melting metallic silicon under vacuum to remove the phosphorus contained therein by evaporation, and then carrying put solidification of the residue for the removal of the impurity elements from the moltan silicon, thereby obtaining a first ingot;
B: removing the impurity concentrated portion of the first ingot by cutting:
C: re-melting the remaining portion, removing boron and abrbon from the melt by oxidizing under an oxidizing atmosphere, and in succession, blowing an argon gas or a mixed gas of argon and hydrogen into the melt for deoxidixation;
D: casting the deoxidized melt in a mold, followed by directional solidification to obtain a second ingot; and E: removing the impurity concentrated portion of the second ingot by cutting.
A: melting metallic silicon under vacuum to remove the phosphorus contained therein by evaporation, and then carrying put solidification of the residue for the removal of the impurity elements from the moltan silicon, thereby obtaining a first ingot;
B: removing the impurity concentrated portion of the first ingot by cutting:
C: re-melting the remaining portion, removing boron and abrbon from the melt by oxidizing under an oxidizing atmosphere, and in succession, blowing an argon gas or a mixed gas of argon and hydrogen into the melt for deoxidixation;
D: casting the deoxidized melt in a mold, followed by directional solidification to obtain a second ingot; and E: removing the impurity concentrated portion of the second ingot by cutting.
2. A process according to claim 1, wherein said metallic silicon is obtained by reductive smelting of silicon oxide.
3. A grocess for the production of polycrystalline silicon, which comprises transferring metallic silicon under molten state, which has been obtained by reductive smelting of silicon oxide, into a crucible, removing boron and carbon by oxidizing under an oxidizing atmosphere, carrying out solidification, and effecting the step B according to claim 1, melting under vacuum and the steps C, D and E according to claim 1.
4. A process according to any one of claims 1 to 3, wherein the above-described oxidizing atmosphere is formed from an H2O, CO2 or O2 gas in an amount small enough so that the interface between the melt and the gas is covered with silicon oxide.
5. A process according to claim 4, wherein silicon oxide formed on the surface of the melt is removed by locally heating by plasma arc.
6. A process according to any one of claims 1 to 5, wherein an H2O, CO2 or O2 gas is blown into the melt instead of placing the melt under said oxidizing atmosphere.
7. A process according to any one of claims 1 to 6, wherein SiO2 or Si3N4 is used as a mold releasing agent.
8. A process according to any one of claims 1 to 7, wherein a solidification interface moving rate is set at mm/min or less fo the removal of impurities, and a solidification interface moving rate for directional solidification is set at 2 mm/min or less.
9. A process according to any one of claims 1 to 8, wherein said ingot is cut at a height at least 70% above the bottom of the ingot.
10. A process according to any one of claims 1 to 9, wherein the phosphorus concentration of the melt is set at 0.3 ppm or less.
11. A process according to any one of claims 1 to 10, wherein the boron concentration of the melt is set at 0.6 ppm or less.
12. A process according to any one of claims 1 to 11, wherein the carbon concentration of the melt is set at 10 ppm or less.
13. An apparatus for manufacturing polycrystalline silicon, which comprises heating means for melting or heating metallic silicon, a retaining container for retaining the melt, a first mold into which the melt is cast from the retaining container, a vacuum chamber for removing phosphorus by evaporation, said chamber surrounding the retaining container and the first mold, means for removing an impurity concentrated portion of an. ingot from the first mold, re-melting means for re-melting or heating a portion of said ingot from the first mold containing fewer impurities, a smelting container for retaining the re-melt, a nozzle for blowing or spraying an oxidizing gas, hydrogen gas or a mixed gas of hydrogen and argon to re-melt in the smelting container an a second mold for forming the deoxidized re-melt into a cast ingot.
14. An apparatus according to claim 13, wherein the degree of vacuum in the vacuum chamber is set at 10-3 torr or higher.
15. An apparatus according to claim 13 or 14, wherein the retaining container is a water-cooling jacket made of copper or graphite crucible; and the smelting container is a crucible made of SiO2, or an SiO2 stamped crucible or SiO2 lined crucible.
16. An apparatus according to any one of claims 13 to 15, wherein said heating means is an electron gun.
17. An apparatus according to any one of claims 13 to 16, wherein said re-melting means is a plasma torch or a DC
arc source.
arc source.
18. An apparatus according to any one of claims 13 to 17, wherein said first and second molds have side walls formed of a heat insulating material and have a bottom formed of a water-cooled jacked; a heating source for heating the melt is disposed above the casts.
19. An apparatus according to any one of claims 13 to 18, wherein W/H ratio, that is, the ratio of the diameter W
to the height H of said cast is set at greater than 0.5.
to the height H of said cast is set at greater than 0.5.
20. A process for the production of a silicon wafer for solar cell, which comprises slicing an ingot of polycrystalline silicon obtained in any one of the processes according to claims 1 to 12.
21. A process according to claim 20, the above-described thin plate has a thickness of 100 to 450 m.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA002211028A CA2211028C (en) | 1996-10-14 | 1996-10-14 | Process and apparatus for manufacturing polycrystalline silicon, and process for manufacturing silicon wafer for solar cell |
| EP96933633A EP0869102B1 (en) | 1996-10-14 | 1996-10-14 | Process and apparatus for preparing polycrystalline silicon and process for preparing silicon substrate for solar cell |
| PCT/JP1996/002965 WO1998016466A1 (en) | 1996-10-14 | 1996-10-14 | Process and apparatus for preparing polycrystalline silicon and process for preparing silicon substrate for solar cell |
| NO974454A NO974454L (en) | 1996-10-14 | 1997-09-26 | Process and apparatus for producing polycrystalline silicon and process for producing silicon plates for solar cells |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA002211028A CA2211028C (en) | 1996-10-14 | 1996-10-14 | Process and apparatus for manufacturing polycrystalline silicon, and process for manufacturing silicon wafer for solar cell |
| PCT/JP1996/002965 WO1998016466A1 (en) | 1996-10-14 | 1996-10-14 | Process and apparatus for preparing polycrystalline silicon and process for preparing silicon substrate for solar cell |
| NO974454A NO974454L (en) | 1996-10-14 | 1997-09-26 | Process and apparatus for producing polycrystalline silicon and process for producing silicon plates for solar cells |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2211028A1 CA2211028A1 (en) | 1998-04-14 |
| CA2211028C true CA2211028C (en) | 2002-04-16 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002211028A Expired - Fee Related CA2211028C (en) | 1996-10-14 | 1996-10-14 | Process and apparatus for manufacturing polycrystalline silicon, and process for manufacturing silicon wafer for solar cell |
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| Country | Link |
|---|---|
| CA (1) | CA2211028C (en) |
| NO (1) | NO974454L (en) |
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|---|---|---|---|---|
| CN100444410C (en) * | 2006-05-08 | 2008-12-17 | 高文秀 | P-type solar cell grade polycrystalline silicon preparing process |
| WO2017062571A2 (en) | 2015-10-09 | 2017-04-13 | Milwaukee Silicon, Llc | Purified silicon, devices and systems for producing same |
-
1996
- 1996-10-14 CA CA002211028A patent/CA2211028C/en not_active Expired - Fee Related
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1997
- 1997-09-26 NO NO974454A patent/NO974454L/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| NO974454D0 (en) | 1997-09-26 |
| CA2211028A1 (en) | 1998-04-14 |
| NO974454L (en) | 1998-04-23 |
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