WO2012098598A1 - 多結晶シリコン製造装置および多結晶シリコンの製造方法 - Google Patents
多結晶シリコン製造装置および多結晶シリコンの製造方法 Download PDFInfo
- Publication number
- WO2012098598A1 WO2012098598A1 PCT/JP2011/005283 JP2011005283W WO2012098598A1 WO 2012098598 A1 WO2012098598 A1 WO 2012098598A1 JP 2011005283 W JP2011005283 W JP 2011005283W WO 2012098598 A1 WO2012098598 A1 WO 2012098598A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- gas supply
- gas
- polycrystalline silicon
- supply nozzle
- bottom plate
- Prior art date
Links
Images
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/455—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
- C23C16/45563—Gas nozzles
-
- 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
- C01B33/027—Preparation by decomposition or reduction of gaseous or vaporised silicon compounds other than silica or silica-containing material
- C01B33/035—Preparation by decomposition or reduction of gaseous or vaporised silicon compounds other than silica or silica-containing material by decomposition or reduction of gaseous or vaporised silicon compounds in the presence of heated filaments of silicon, carbon or a refractory metal, e.g. tantalum or tungsten, or in the presence of heated silicon rods on which the formed silicon is deposited, a silicon rod being obtained, e.g. Siemens process
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/22—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
- C23C16/24—Deposition of silicon only
Definitions
- the present invention relates to polycrystalline silicon manufacturing technology, and more particularly, to a source gas supply nozzle installation location of a reactor for producing polycrystalline silicon by the Siemens method and flow velocity control of the raw material gas.
- Polycrystalline silicon is used as a raw material of a single crystal silicon substrate for manufacturing a semiconductor device and a substrate for manufacturing a solar cell.
- the Siemens method is known as a method of producing polycrystalline silicon.
- the Siemens method is a method in which a raw material gas containing chlorosilane is brought into contact with a heated silicon core wire, and thereby polycrystalline silicon is vapor-phase grown on the surface of the silicon core wire by a CVD method to obtain a silicon rod.
- reaction temperature the temperature of the surface of the silicon rod to moderate the precipitation reaction
- the major factors that affect the deposition rate in the deposition reaction of polycrystalline silicon are the surface temperature of the silicon rod, the concentration of chlorosilane in the reaction gas in the reactor, and the flow rate of the reaction gas near the surface of the silicon rod. It is important to control these factors under a proper balance in order to reduce unevenness of the silicon rod surface and maintain a good surface. Specifically, it is necessary to increase the gas flow rate on the surface of the silicon rod to reduce the surface unevenness while increasing the surface temperature of the silicon rod to keep the deposition reaction rate high to a certain extent.
- the local reaction gas temperature exceeds 600 ° C, a large amount of powder may be generated in the furnace due to chlorosilane byproducts, which may cause heavy metal contamination or protrusion-like abnormal growth on the silicon rod surface. It will be.
- the surface temperature of the polycrystalline silicon rod during the precipitation reaction is as high as about 900 to 1200.degree. Therefore, if the local circulation of the reaction gas in the reactor is continued, the temperature of the reaction gas will rise to about 900 to 1200 ° C., which is the same as the temperature of the silicon rod surface. Therefore, in order to keep the reaction gas temperature at about 600 ° C. or less, it is necessary to efficiently cool the reaction gas during circulation in the reaction furnace.
- the present invention has been made in view of the above problems, and the object of the present invention is to efficiently generate a large amount of circulating flow in the reactor and form a high-speed reaction gas flow in the reactor.
- the reaction gas flow rate near the polycrystalline silicon rod is secured, the local rise of the gas temperature in the reactor is prevented, the popcorn generation on the polycrystalline silicon surface is suppressed even though it is the high speed precipitation reaction, and the powder is generated.
- An object of the present invention is to provide a technology for obtaining a polycrystalline silicon rod free of heavy metal contamination and protruding abnormal deposition.
- Raw gas exit can be controlled by the above flow rate 150 meters / sec, and wherein the.
- the gas supply nozzles other than the gas supply nozzle disposed at the center of the bottom plate are disposed at the apex of a regular polygon inscribed in a second virtual concentric circle having a center at the center of the bottom plate There is.
- the height of the internal space of the bell jar provided in the reactor is 2 m or more and 5 m or less, and the radius of the second virtual concentric circle is 20 to 70 cm.
- the regular polygon is a regular n-gon (n is an integer of 3 or more and 8 or less).
- the diameter of the gas injection hole of the gas supply nozzle is 7 mm ⁇ to 20 mm ⁇ .
- the raw material gas is ejected from the gas supply nozzle at a flow velocity of 150 m / sec or more using the above-described polycrystalline silicon manufacturing apparatus to deposit polycrystalline silicon on the surface of the silicon core wire.
- the ejection amount of the source gas per nozzle of the gas supply nozzle is set to 300 kg / hr or more.
- the circulating flow in the reactor is caused by the source gas ejected from the source gas supply nozzle disposed inside the imaginary concentric circle.
- the formation of an appropriately high temperature zone due to the generation of a locally closed circulating flow in the reactor is suppressed, because polycrystals are clearly divided and formed into the updraft and downdraft along the inner wall of the reactor.
- the generation of popcorn on the silicon surface can be suppressed to obtain high quality polycrystalline silicon.
- the reaction gas flow around the polycrystalline silicon rod can be efficiently maintained at a relatively high speed
- the high-speed precipitation reaction can be performed by increasing the amount of the source gas without using the high-speed circulation even though the high-speed precipitation reaction is performed. It also becomes possible to solve the problem of the cost increase that the conventional method has.
- positioning of the source gas supply nozzle and reaction waste-gas port which are provided in the reactor with which the polycrystalline-silicon manufacturing apparatus of invention is equipped by illustration. It is the upper surface schematic of the baseplate for demonstrating the other aspect of arrangement
- FIG. 1 is a schematic cross-sectional view for explaining a structural example of a reaction furnace provided in a polycrystalline silicon manufacturing apparatus of the present invention.
- the inside of the reactor 100 is sealed by a bell jar 1 provided with a viewing window 2 for confirming the internal state and a bottom plate 5, and a plurality of silicon core wires 12 assembled in a torii type are arranged in the sealed space.
- Polycrystalline silicon is deposited on the surface of the silicon core wire (or silicon rod 13).
- the bottom plate 5 is provided with a core holder 11 and a metal electrode 10 for generating heat by applying electricity from both ends of the silicon core 12, a nozzle 9 for supplying a source gas to the inside of the bell jar 1, and gas after reaction.
- a reaction exhaust gas outlet 8 for exhausting to the outside is provided.
- a raw material gas whose flow rate and flow rate are controlled by the gas flow rate control unit 14 is supplied from the blowout port of the nozzle 9. Further, as shown in FIG. 1, although it is preferable to provide a plurality of nozzles 9, it may be a single nozzle.
- the bottom plate 5 has a disk shape, and in many cases, the metal electrode 10, the nozzle 9, and the reaction exhaust gas port 8 provided on the bottom plate 5 are also arranged concentrically.
- a source gas a mixed gas of trichlorosilane and hydrogen is often used, and the reaction temperature is also relatively high at 900 ° C. to 1200 ° C. Therefore, the refrigerant inlet 3 and the refrigerant outlet 4 are provided at the lower and upper portions of the bell jar 1, and the refrigerant inlet 6 and the refrigerant outlet 7 are provided at both ends of the bottom plate 5, respectively.
- a refrigerant is supplied to perform cooling.
- water is generally used as such a refrigerant
- the inner surface temperature of the bell jar 1 at the time of the precipitation reaction is approximately 100 ° C. to 400 ° C.
- FIGS. 2 and 3 are schematic top views of the bottom plate 5 for illustrating the arrangement of the raw material gas supply nozzle 9 and the reaction exhaust gas port 8 provided in the reaction furnace provided in the polycrystalline silicon production apparatus of the present invention. is there.
- the raw material gas supply nozzle 9 is disposed inside this concentric circle C. Further, an estimated imaginary line indicating the horizontal spread of the jet flow from the gas supply nozzle 9 is indicated by a broken line with a symbol D. From the gas supply nozzle 9, the raw material gas is ejected into the bell jar 1 at a flow velocity of 150 m / sec or more except for the initial stage of the reaction described later.
- the arrangement position of the reaction exhaust gas port 8 is not particularly limited, but in the aspect shown in FIG. 2 and FIG. 3, it is installed outside the concentric circle C.
- gas supply nozzle 9 is provided in the example shown in FIG. 2 and four gas supply nozzles 9 are provided in the example shown in FIG. 3, the gas supply nozzle 9 is located inside the concentric circle C in any case. Be placed.
- the gas supply nozzle 9 is provided at the center of the bottom plate 5.
- Three gas supply nozzles 9 are disposed.
- FIG. 4 (A) to 4 (E) are schematic top views of the bottom plate for illustrating another embodiment of the arrangement of the raw material gas supply nozzle and the reaction exhaust gas port provided in the reaction furnace included in the polycrystalline silicon manufacturing apparatus of the invention.
- FIGS. 4 (A) to 4 (E) there are five (FIG. 4 (A)), six (FIG. 4 (B)), seven (FIG. 4 (C)) gas supply nozzles 9 respectively. ), Eight (FIG. 4 (D)), nine (FIG. 4 (E)) are provided.
- the raw material gas supply nozzle 9 is disposed inside the concentric circle C, and in addition to the gas supply nozzle 9 provided at the central portion of the bottom plate 5, the central portion gas supply nozzle 9 is The remaining gas supply nozzles 9 are disposed at the positions of the apexes of the regular polygon inscribed in the circumscribed circle E (the second virtual concentric circle) that is the center.
- FIG. 5 and FIG. 6 are schematic top views of the bottom plate 5 for illustrating another aspect of the arrangement of the raw material gas supply nozzle 9 and the reaction exhaust gas port 8 provided in the reaction furnace as a reference example.
- the gas supply nozzle 9 is disposed inside the concentric circle C, the gas supply nozzle 9 is not provided at the center of the bottom plate 5 (FIG. 5), or substantially uniformly on the bottom plate 5.
- the gas supply nozzle 9 is not disposed at the position of the apex of the regular polygon in contact with the circumscribed circle E centered on the gas supply nozzle 9 in the central portion (FIG. 6).
- FIGS. 2 to 4 an aspect (FIG. 2) of providing the gas supply nozzle 9 at the central part of the bottom plate 5 or In the embodiment (FIGS. 3 to 4) in which the gas supply nozzle 9 is arranged at the position of the apex of the regular polygon in contact with the circumscribed circle E centered on the gas supply nozzle 9 of FIG.
- FIGS. 3 to 4 an aspect of providing the gas supply nozzle 9 at the central part of the bottom plate 5 or In the embodiment (FIGS. 3 to 4) in which the gas supply nozzle 9 is arranged at the position of the apex of the regular polygon in contact with the circumscribed circle E centered on the gas supply nozzle 9 of FIG.
- a stable updraft is obtained
- the peripheral portion of the bottom plate 5 a stable downdraft is obtained.
- a smooth circulating flow is formed in the bell jar.
- the reason can be considered as follows. As described above, when the gas supply nozzles 9 are arranged inside the concentric circle C, the high flow velocity source gas spouted from the gas supply nozzles 9 ascends with the surrounding reaction gas. This ascending gas flow collides with the upper inner wall of the bell jar 1 to change the flow downward, and becomes a circulating flow and descends along the inner wall of the bell jar. Then, part of the descending gas flow again rises in the reaction space together with the source gas ejected from the gas supply nozzle 9. In this way, a clear circulating flow is formed by defining the updraft area and the downdraft area throughout the reactor. As a result, the occurrence of a high temperature region in which the temperature of the source gas rises to an inappropriate temperature locally is suppressed.
- the number of the gas supply nozzles 9 may be one at the center of the bottom plate 5, Alternatively, in addition to one of the central portions of the bottom plate 5, it is preferable to arrange the remaining gas supply nozzle 9 at the position of the apex of a regular polygon having a radius of the circumscribed circle E of 20 to 70 cm.
- FIGS. 7A and 7B are views for schematically explaining the flow in the bell jar 1 of the raw material gas ejected from the gas supply nozzle 9 arranged in the mode shown in FIGS. 2 and 3, respectively.
- the outline of the gas flow when the source gas is supplied at 150 m / sec or more is shown.
- the high flow rate raw material gas spouted from the gas supply nozzle 9 arranged in the above-described manner rises while entraining the surrounding reaction gas, collides with the upper inner wall of the bell jar 1 and descends.
- the gas supply nozzle 9 As described above, by disposing the gas supply nozzle 9 inside the concentric circle C, the raw material gas with a high flow velocity spouted from the gas supply nozzle 9 ascends with the surrounding reaction gas. Then, the ascending gas flow collides with the upper inner wall of the bell jar 1 to change the flow downward, and becomes a circulating flow and descends along the inner wall of the bell jar 1, and a part of the descending gas flow is supplied again to the gas.
- the inside of the reaction space is raised together with the raw material gas ejected from the nozzle 9. Such smooth circulating flow of gas suppresses the occurrence of a high temperature region locally.
- the polycrystalline silicon rod 13 provided in the vicinity of the gas supply nozzle 9 directly receives the upward flow of the raw material gas ejected from the gas supply nozzle 9, but such polycrystalline silicon rod 13 is Only a part of what is installed in the reactor, and many other polycrystalline silicon rods 13 will receive a smooth circulating gas flow consisting of the rising gas flow and the entrained reaction gas flow.
- the gas supply nozzle is not provided at the central portion of the bottom plate 5, and as a result, in the embodiment in which the distance between the gas supply nozzles is wide, A downward circulation flow is formed.
- Such downward circulating flow rises again in the reaction space while remaining at a high temperature without being cooled by the inner wall (inner wall temperature 150 to 400 ° C.) of the bell jar 1.
- Such gas circulation causes the shape abnormality of the polycrystalline silicon rod and the generation of popcorn or powder.
- the jetted gas does not reach the upper portion of the reactor and circulates only in the lower portion of the reactor.
- a stagnant part of the reaction gas is generated at the upper part of the reactor.
- Such stagnation of the reaction gas raises the temperature of the gas, which causes an abnormality in the shape of the polycrystalline silicon rod and generation of popcorn or powder.
- the flow rate of the gas supplied from the gas supply nozzle 9 at the initial stage of the precipitation reaction is preferably kept relatively low. This is because, since the diameter of the polycrystalline silicon rod 13 at the initial stage of the precipitation reaction is thin, if the gas is supplied at a high speed, the polycrystalline silicon rod 13 may fall over due to the impact. Then, after the diameter of the polycrystalline silicon rod 13 has increased to a certain extent (for example, after becoming a diameter of about 20 mm or more), 150 m / sec to form a smooth circulating flow in the reactor as described above It is preferable to supply the source gas at the above flow rate.
- a smooth circulating flow is formed by the above-described arrangement of the gas supply nozzles, and a sufficiently fast reaction gas flow is formed in the furnace even with the supply of the source gas at a flow velocity of about 150 m / sec. be able to. That is, according to the present invention in which a large amount of circulating flow is formed in the reaction furnace, a high-speed reaction gas flow can be formed in the furnace even when the supply flow rate of the raw material gas is lower than that in the prior art. As a result, the supply amount of the source gas is suppressed.
- the raw material gas when supplied at a flow rate of about 150 m / s, it is estimated that the raw material gas is supplied to the surface of any silicon rod installed in the furnace at an average flow rate of about 3 m / s. However, this flow rate is sufficient for realizing high-speed precipitation reaction.
- the raw material gas is supplied at a flow velocity of 150 m / sec or more, but the width of the internal space of the bell jar 1 of the apparatus used is general (height 2-3 m, diameter 1-3 m Assuming that the reaction pressure is, for example, 0.3 MPa to 0.9 MPa, it is preferable to set the raw material gas injection amount per gas supply nozzle to 300 kg / hr or more.
- the number of gas supply nozzles is preferably 1 to 9, and the diameter of the nozzle holes (gas injection holes) is preferably 7 mm ⁇ to 20 mm ⁇ .
- FIG. 9 is a schematic cross-sectional view showing an example of the gas supply nozzle according to the present invention.
- the material of the nozzle tip 9a is preferably a metal such as SUS, Ni, Cu or the like, or ceramic, carbon or the like.
- Example 1 a polycrystalline silicon rod was manufactured using one in which the gas supply nozzle 9 was disposed in the manner shown in FIG.
- Example 2 a polycrystalline silicon rod was manufactured using one in which the gas supply nozzle 9 was disposed in the mode illustrated in FIG. 4C.
- Comparative Example 1 a polycrystalline silicon rod was manufactured using one in which the gas supply nozzle 9 was disposed in the manner shown in FIG.
- the gas supply nozzle 9 was disposed in the manner shown in FIG.
- six gas supply nozzles 9 are provided inside the concentric circle C at equal distances on concentric circles centered on the center of the bottom plate, but no nozzles are arranged at the center of the bottom plate.
- Comparative Example 2 a polycrystalline silicon rod was manufactured using one in which the gas supply nozzle 9 was disposed in the manner illustrated in FIG.
- the gas supply nozzles 9 are disposed inside the concentric circle C at substantially even intervals on the substantially entire surface of the bottom plate.
- a polycrystalline silicon rod was manufactured using the same gas supply nozzle 9 arrangement as in Example 1, but using a nozzle whose diameter was increased to make the ejection flow velocity of the source gas less than 150 m / sec. .
- a polycrystalline silicon rod was manufactured using the same gas supply nozzle 9 arrangement as in Example 2 but using a nozzle whose diameter was increased to make the ejection flow velocity of the source gas less than 150 m / sec. .
- Tables 1 to 3 are tables summarizing the deposition reaction conditions of the above-mentioned Examples 1 to 2 and Comparative Examples 1 to 2 and Comparative Examples 3 to 4 and the evaluation results of the obtained polycrystalline silicon rods, respectively. .
- the reaction temperature, reaction pressure, source gas type, source gas concentration, total feed amount of source material per time, and final polycrystalline silicon rod diameter obtained by production were all the same.
- the circulating flow in the reaction furnace rises at the center of the reaction furnace by the raw material gas ejected from the raw material gas supply nozzle disposed inside the virtual concentric circle. Since the air flow and the downdraft along the inner wall of the reactor are clearly divided and formed, the formation of an inappropriate high temperature region due to the generation of a circulating flow locally closed in the reactor is suppressed, and the polycrystalline silicon surface is formed. It is possible to obtain high quality polycrystalline silicon by suppressing the generation of popcorn.
- the reaction gas flow around the polycrystalline silicon rod can be efficiently maintained at a relatively high speed
- the high-speed precipitation reaction can be performed by increasing the amount of the source gas without using the high-speed circulation even though the high-speed precipitation reaction is performed. It also becomes possible to solve the problem of the cost increase that the conventional method has.
- the present invention efficiently generates a large amount of circulating flow in the reactor to form a high-speed reaction gas flow in the reactor, thereby securing the flow velocity of the reactant gas in the vicinity of the polycrystalline silicon rod, and the gas temperature in the reactor
- the present invention provides a technology for obtaining a polycrystalline silicon rod without heavy metal contamination due to powder generation and protrusion-like abnormal deposition, while preventing the local rise of and suppressing the generation of popcorn on the surface of polycrystalline silicon even with high-speed precipitation reaction.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Silicon Compounds (AREA)
Abstract
Description
1 ベルジャ
2 のぞき窓
3 冷媒入口(ベルジャ)
4 冷媒出口(ベルジャ)
5 底板
6 冷媒入口(底板)
7 冷媒出口(底板)
8 反応排ガス出口
9 ガス供給ノズル
9a ノズルチップ
10 電極
11 芯線ホルダ
12 シリコン芯線
13 多結晶シリコン棒
14 ガス流量制御部
Claims (7)
- シーメンス法により多結晶シリコンを製造するための多結晶シリコン製造装置であって、
ベルジャと円盤状の底板とにより内部が密閉される反応炉と、
前記ベルジャ内部に所望の流量で原料ガスを供給するガス流量制御部と、を備え、
前記底板には、複数のシリコン芯線に通電するための電極対と、前記ベルジャの内部空間に原料ガスを供給するためのガス供給ノズルが少なくとも1つ設けられており、
前記ガス供給ノズルは、前記底板の中央に中心を有する仮想同心円であって前記円盤状の底板の面積S0の半分の面積S(=S0/2)を有する仮想の同心円の内側に配置され、且つ、前記ガス供給ノズルの1つは前記底板の中央に配置されており、
前記ガス流量制御部は、前記ガス供給ノズルからの噴出原料ガスを150m/sec以上の流速で制御可能である、
ことを特徴とする多結晶シリコン製造装置。 - 前記底板の中央に配置されているガス供給ノズルを除くガス供給ノズルは、前記底板の中央に中心を有する第2の仮想同心円に内接する正多角形の頂点の位置に配置されている、
請求項1に記載の多結晶シリコン製造装置。 - 前記反応炉が備えるベルジャの内部空間の高さは2m以上5m以下であり、
前記第2の仮想同心円の半径は20~70cmである、
請求項2に記載の多結晶シリコン製造装置。 - 前記正多角形は正n角形(nは3以上で8以下の整数)である、請求項2に記載の多結晶シリコン製造装置。
- 前記ガス供給ノズルのガス噴出孔の直径は7mmφ~20mmφである、請求項1乃至4の何れか1項に記載の多結晶シリコン製造装置。
- 請求項1乃至4の何れか1項に記載の多結晶シリコン製造装置を用い、前記ガス供給ノズルから150m/sec以上の流速で原料ガスを噴出させて前記シリコン芯線の表面に多結晶シリコンを析出させる、多結晶シリコンの製造方法。
- 前記ガス供給ノズルの1本当たりの原料ガスの噴出量を300kg/hr以上とする、請求項6に記載の多結晶シリコンの製造方法。
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13/979,789 US9416444B2 (en) | 2011-01-21 | 2011-09-20 | Apparatus for producing polycrystalline silicon and method for producing polycrystalline silicon |
CN201180065676.3A CN103328380B (zh) | 2011-01-21 | 2011-09-20 | 多晶硅制造装置及多晶硅的制造方法 |
KR1020137013247A KR101678265B1 (ko) | 2011-01-21 | 2011-09-20 | 다결정 실리콘 제조 장치 및 다결정 실리콘의 제조 방법 |
JP2012553468A JP5739456B2 (ja) | 2011-01-21 | 2011-09-20 | 多結晶シリコン製造装置および多結晶シリコンの製造方法 |
US15/206,070 US20160319430A1 (en) | 2011-01-21 | 2016-07-08 | Apparatus for producing polycrystalline silicon and method for producing polycrystalline silicon |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2011010493 | 2011-01-21 | ||
JP2011-010493 | 2011-01-21 |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US13/979,789 A-371-Of-International US9416444B2 (en) | 2011-01-21 | 2011-09-20 | Apparatus for producing polycrystalline silicon and method for producing polycrystalline silicon |
US15/206,070 Division US20160319430A1 (en) | 2011-01-21 | 2016-07-08 | Apparatus for producing polycrystalline silicon and method for producing polycrystalline silicon |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2012098598A1 true WO2012098598A1 (ja) | 2012-07-26 |
Family
ID=46515253
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2011/005283 WO2012098598A1 (ja) | 2011-01-21 | 2011-09-20 | 多結晶シリコン製造装置および多結晶シリコンの製造方法 |
Country Status (6)
Country | Link |
---|---|
US (2) | US9416444B2 (ja) |
JP (1) | JP5739456B2 (ja) |
KR (1) | KR101678265B1 (ja) |
CN (1) | CN103328380B (ja) |
MY (1) | MY163182A (ja) |
WO (1) | WO2012098598A1 (ja) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014061212A1 (ja) | 2012-10-16 | 2014-04-24 | 信越化学工業株式会社 | 多結晶シリコン製造用原料ガスの供給方法および多結晶シリコン |
WO2016035249A1 (ja) * | 2014-09-04 | 2016-03-10 | 信越化学工業株式会社 | 多結晶シリコン製造用反応炉、多結晶シリコン製造装置、多結晶シリコンの製造方法、及び、多結晶シリコン棒または多結晶シリコン塊 |
JP2016510305A (ja) * | 2013-03-18 | 2016-04-07 | ワッカー ケミー アクチエンゲゼルシャフトWacker Chemie AG | 多結晶シリコンの堆積法 |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8961689B2 (en) * | 2008-03-26 | 2015-02-24 | Gtat Corporation | Systems and methods for distributing gas in a chemical vapor deposition reactor |
CN105271241B (zh) * | 2014-06-26 | 2019-05-14 | 江苏中能硅业科技发展有限公司 | 用于生产多晶硅的反应器 |
DE102015219925A1 (de) * | 2015-10-14 | 2017-04-20 | Wacker Chemie Ag | Reaktor zur Abscheidung von polykristallinem Silicium |
CN107497392B (zh) * | 2017-10-11 | 2019-07-16 | 中石化上海工程有限公司 | 喷射反应器管口喷嘴 |
EP3763673B1 (en) * | 2018-04-05 | 2023-04-19 | Tokuyama Corporation | Polycrystalline silicon rod manufacturing method, and reactor |
CN110255565A (zh) * | 2019-07-05 | 2019-09-20 | 江苏双良新能源装备有限公司 | 一种大型还原炉底盘 |
CN114212794B (zh) * | 2021-12-30 | 2023-03-28 | 新疆大全新能源股份有限公司 | 制备电子级方硅芯的原生多晶硅棒的生产方法 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008156212A (ja) * | 2006-11-29 | 2008-07-10 | Mitsubishi Materials Corp | トリクロロシラン製造装置 |
WO2010098319A1 (ja) * | 2009-02-27 | 2010-09-02 | 株式会社トクヤマ | 多結晶シリコンロッド及びその製造装置 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002241120A (ja) | 2001-02-15 | 2002-08-28 | Sumitomo Titanium Corp | 多結晶シリコン製造用反応炉及び多結晶シリコン製造方法 |
JP2006206387A (ja) | 2005-01-28 | 2006-08-10 | Mitsubishi Materials Corp | 多結晶シリコン還元炉及び多結晶シリコンロッド |
WO2006110481A2 (en) * | 2005-04-10 | 2006-10-19 | Rec Silicon Inc | Production of polycrystalline silicon |
CN102143909A (zh) * | 2008-09-09 | 2011-08-03 | 智索株式会社 | 高纯度结晶硅、高纯度四氯化硅及其制造方法 |
CN101683975B (zh) * | 2008-09-16 | 2013-09-25 | 三菱麻铁里亚尔株式会社 | 多晶硅制备用碳部件的净化方法 |
US20110229638A1 (en) * | 2010-03-19 | 2011-09-22 | Gt Solar Incorporated | System and method for polycrystalline silicon deposition |
JP5633174B2 (ja) | 2010-04-12 | 2014-12-03 | 三菱マテリアル株式会社 | 多結晶シリコンロッド |
-
2011
- 2011-09-20 KR KR1020137013247A patent/KR101678265B1/ko active IP Right Grant
- 2011-09-20 MY MYPI2013701160A patent/MY163182A/en unknown
- 2011-09-20 JP JP2012553468A patent/JP5739456B2/ja active Active
- 2011-09-20 WO PCT/JP2011/005283 patent/WO2012098598A1/ja active Application Filing
- 2011-09-20 US US13/979,789 patent/US9416444B2/en active Active
- 2011-09-20 CN CN201180065676.3A patent/CN103328380B/zh active Active
-
2016
- 2016-07-08 US US15/206,070 patent/US20160319430A1/en not_active Abandoned
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008156212A (ja) * | 2006-11-29 | 2008-07-10 | Mitsubishi Materials Corp | トリクロロシラン製造装置 |
WO2010098319A1 (ja) * | 2009-02-27 | 2010-09-02 | 株式会社トクヤマ | 多結晶シリコンロッド及びその製造装置 |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014061212A1 (ja) | 2012-10-16 | 2014-04-24 | 信越化学工業株式会社 | 多結晶シリコン製造用原料ガスの供給方法および多結晶シリコン |
JP2014080315A (ja) * | 2012-10-16 | 2014-05-08 | Shin Etsu Chem Co Ltd | 多結晶シリコン製造用原料ガスの供給方法および多結晶シリコン |
CN104736480A (zh) * | 2012-10-16 | 2015-06-24 | 信越化学工业株式会社 | 多晶硅制造用原料气体的供给方法和多晶硅 |
US9263261B2 (en) | 2012-10-16 | 2016-02-16 | Shin-Etsu Chemical Co., Ltd. | Method for supplying source gas for producing polycrystalline silicon and polycrystalline silicon |
EP2910525A4 (en) * | 2012-10-16 | 2016-04-13 | Shinetsu Chemical Co | METHOD FOR SUPPLYING SOURCE GAS TO PRODUCE POLYCRYSTALLINE SILICON AND POLYCRYSTALLINE SILICON |
CN104736480B (zh) * | 2012-10-16 | 2017-03-08 | 信越化学工业株式会社 | 多晶硅制造用原料气体的供给方法和多晶硅 |
JP2016510305A (ja) * | 2013-03-18 | 2016-04-07 | ワッカー ケミー アクチエンゲゼルシャフトWacker Chemie AG | 多結晶シリコンの堆積法 |
WO2016035249A1 (ja) * | 2014-09-04 | 2016-03-10 | 信越化学工業株式会社 | 多結晶シリコン製造用反応炉、多結晶シリコン製造装置、多結晶シリコンの製造方法、及び、多結晶シリコン棒または多結晶シリコン塊 |
JP2016052970A (ja) * | 2014-09-04 | 2016-04-14 | 信越化学工業株式会社 | 多結晶シリコン製造用反応炉、多結晶シリコン製造装置、多結晶シリコンの製造方法、及び、多結晶シリコン棒または多結晶シリコン塊 |
US10858258B2 (en) | 2014-09-04 | 2020-12-08 | Shin-Etsu Chemical Co., Ltd. | Reaction furnace for producing polycrystalline silicon, apparatus for producing polycrystalline silicon, method for producing polycrystalline silicon, and polycrystalline silicon rod or polycrystalline silicon ingot |
US10870581B2 (en) | 2014-09-04 | 2020-12-22 | Shin-Etsu Chemical Co., Ltd. | Reaction furnace for producing polycrystalline silicon, apparatus for producing polycrystalline silicon, method for producing polycrystalline silicon, and polycrystalline silicon rod or polycrystalline silicon ingot |
Also Published As
Publication number | Publication date |
---|---|
US9416444B2 (en) | 2016-08-16 |
CN103328380A (zh) | 2013-09-25 |
US20130302528A1 (en) | 2013-11-14 |
MY163182A (en) | 2017-08-15 |
KR101678265B1 (ko) | 2016-11-21 |
KR20140002648A (ko) | 2014-01-08 |
JPWO2012098598A1 (ja) | 2014-06-09 |
CN103328380B (zh) | 2016-09-21 |
US20160319430A1 (en) | 2016-11-03 |
JP5739456B2 (ja) | 2015-06-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2012098598A1 (ja) | 多結晶シリコン製造装置および多結晶シリコンの製造方法 | |
JP5699060B2 (ja) | 多結晶シリコンの製造方法 | |
US10870581B2 (en) | Reaction furnace for producing polycrystalline silicon, apparatus for producing polycrystalline silicon, method for producing polycrystalline silicon, and polycrystalline silicon rod or polycrystalline silicon ingot | |
WO2013080556A1 (ja) | 多結晶シリコンの製造方法および多結晶シリコン製造用反応炉 | |
JP5829547B2 (ja) | 多結晶シリコン棒および多結晶シリコン製造装置 | |
US9263261B2 (en) | Method for supplying source gas for producing polycrystalline silicon and polycrystalline silicon | |
JP6147872B2 (ja) | 多結晶シリコンの堆積法 | |
JP5859626B2 (ja) | 多結晶シリコン製造装置および多結晶シリコンの製造方法 | |
JP5642755B2 (ja) | 多結晶シリコンを析出させるための装置及び方法 | |
JP6216029B2 (ja) | 多結晶シリコン棒の製造方法 | |
JP2016029015A (ja) | 多結晶シリコン棒 | |
JP4854639B2 (ja) | 多結晶シリコンの製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 11856251 Country of ref document: EP Kind code of ref document: A1 |
|
ENP | Entry into the national phase |
Ref document number: 2012553468 Country of ref document: JP Kind code of ref document: A |
|
ENP | Entry into the national phase |
Ref document number: 20137013247 Country of ref document: KR Kind code of ref document: A |
|
WWE | Wipo information: entry into national phase |
Ref document number: 13979789 Country of ref document: US |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 11856251 Country of ref document: EP Kind code of ref document: A1 |