WO2005049492A1 - Nanoscale crystalline silicon powder - Google Patents

Nanoscale crystalline silicon powder Download PDF

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Publication number
WO2005049492A1
WO2005049492A1 PCT/EP2004/012890 EP2004012890W WO2005049492A1 WO 2005049492 A1 WO2005049492 A1 WO 2005049492A1 EP 2004012890 W EP2004012890 W EP 2004012890W WO 2005049492 A1 WO2005049492 A1 WO 2005049492A1
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Prior art keywords
silicon powder
sih
crystalline silicon
silane
hydrogen
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PCT/EP2004/012890
Other languages
French (fr)
Inventor
Markus PRIDÖHL
Paul Roth
Hartmut Wiggers
Frank-Martin Petrat
Michael Krämer
Original Assignee
Degussa Ag
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Publication date
Application filed by Degussa Ag filed Critical Degussa Ag
Priority to EP04797876A priority Critical patent/EP1685066B1/en
Priority to AT04797876T priority patent/ATE517059T1/en
Priority to JP2006540274A priority patent/JP4607122B2/en
Priority to UAA200606737A priority patent/UA87672C2/en
Priority to US10/579,460 priority patent/US7776304B2/en
Publication of WO2005049492A1 publication Critical patent/WO2005049492A1/en
Priority to IL175701A priority patent/IL175701A/en
Priority to US12/759,346 priority patent/US8043593B2/en
Priority to US12/829,464 priority patent/US7927570B2/en

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    • 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
    • C01B33/03—Preparation by decomposition or reduction of gaseous or vaporised silicon compounds other than silica or silica-containing material by decomposition of silicon halides or halosilanes or reduction thereof with hydrogen as the only reducing agent
    • 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
    • C01B33/113—Silicon oxides; Hydrates thereof
    • C01B33/12—Silica; Hydrates thereof, e.g. lepidoic silicic acid
    • C01B33/18—Preparation of finely divided silica neither in sol nor in gel form; After-treatment thereof
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82B—NANOSTRUCTURES FORMED BY MANIPULATION OF INDIVIDUAL ATOMS, MOLECULES, OR LIMITED COLLECTIONS OF ATOMS OR MOLECULES AS DISCRETE UNITS; MANUFACTURE OR TREATMENT THEREOF
    • B82B3/00—Manufacture or treatment of nanostructures by manipulation of individual atoms or molecules, or limited collections of atoms or molecules as discrete units
    • 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
    • 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
    • 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
    • C01B33/029—Preparation by decomposition or reduction of gaseous or vaporised silicon compounds other than silica or silica-containing material by decomposition of monosilane
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y40/00—Manufacture or treatment of nanostructures
    • 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
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries
    • 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
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]

Definitions

  • the invention provides a nanoscale crystalline silicon powder and the preparation and use thereof .
  • an aggregated nanoscale silicon powder can be prepared in a hot wall reactor (Roth et al . , Chem. Eng. Technol. 24 (2001), 3).
  • the disadvantage of this process has proven to be that the desired crystalline silicon is produced along with amorphous silicon which is formed by the reaction of silane at the hot reactor walls.
  • the crystalline silicon has a low BET surface area of less than 20 m 2 /g and thus is generally too coarse for electronic applications.
  • the object of the invention is the provision of a silicon powder which avoids the disadvantages of the prior art.
  • the silicon powder should be one with a uniform modification.
  • the invention is also intended to provide a process by which this powder can be prepared on an industrial scale in an economically viable manner.
  • the invention provides an aggregated crystalline silicon powder with a BET surface area of 20 to 150 m/g.
  • the silicon powder according to the invention may have a BET surface area of 40 to 120 m 2 /g.
  • aggregated is understood to mean that the spherical or largely spherical particles which are initially formed in the reaction coalesce to form aggregates during the course of further reaction. The extent of growth may be affected by the process parameters. These aggregates may form agglomerates during the course of further reaction. In contrast to aggregates, which generally cannot or can only partly be broken down into the primary particles, agglomerates form only a loose association of aggregates which can easily be broken down into the aggregates .
  • crystalline is understood to mean that at least 90% of the powder is crystalline. This degree of crystallinity can be determined by comparing the intensities of the [111], [220] and [311] signals of the powder according to the invention with those of a silicon powder of known crystallinity and crystallite size.
  • a silicon powder with a degree of crystallinity of at least 95%, particularly preferably one with at least 98% crystallinity is preferred.
  • the evaluation of TEM images and the counting of primary particles which exhibit lattice lines, as a feature of the crystalline state, is suitable for determining this degree of crystallisation.
  • the silicon powder according to the invention may be doped.
  • the doping components may be phosphorus, arsenic, antimony, bismuth, boron, aluminium, gallium, indium, thallium, europium, erbium, cerium, praseodymium, neodymium, samarium, gadolinium, terbium, dysprosium, holmium, thulium, lutetium, lithium, ytterbium, germanium, iron, ruthenium, osmium, cobalt, rhodium, iridium, nickel, palladium, platinum, copper, silver, gold or zinc.
  • the doping components may be the elements phosphorus, arsenic, antimony, bismuth, boron, aluminium, gallium, indium, thallium, europium, erbium, cerium, praseodymium, neodymium, samarium, gadolinium, terbium, dysprosium, holmium, thulium, ytterbium, lutetium.
  • the proportion of these present in silicon powder according to the invention may be up to 1 wt.%. In general, a silicon powder is required in which the doping component is present in the pp or even the ppb range.
  • silicon powder according to the invention may contain lithium as a doping component.
  • the proportion of lithium present in the silicon powder may be up to 53 wt.%. Silicon powder with up to 20 to 40 wt.% of lithium may be particularly preferred.
  • silicon powder according to the invention may contain germanium as a doping component.
  • the proportion of germanium present in the silicon powder may be up to 40 wt.%. Silicon powder with up to 10 to 30 wt.% of germanium may be particularly preferred.
  • the elements iron, ruthenium, osmium, cobalt, rhodium, iridium, nickel, palladium, platinum, copper, silver, gold, zinc may also be doping components in the silicon powder.
  • the proportion of these present may be up to 5 wt.% of the silicon powder.
  • the doping components may be uniformly distributed in the powder or they may be enriched or intercalated in the shell or the core of the primary particles.
  • the doping components may preferably be incorporated at silicon lattice sites. This depends substantially on the type of doping material and on reaction management.
  • a doping component in the context of the invention is understood to be the element present in the powder according to the invention.
  • a doping material is understood to be the compound used in the process in order to obtain the doping component .
  • the silicon powder according to the invention may also have a hydrogen loading of up to 10 mol.%, wherein a range of 1 to 5 mol.% is particularly preferred.
  • NMR spectroscopic methods such as, for example, 1 H-MAS-NMR spectroscopy or IR spectroscopy are suitable for determining this.
  • the invention also provides a process for preparing the silicon powder according to the invention, characterised in that at least one vaporous or gaseous silane and optionally at least one vaporous or gaseous doping material, an inert gas and hydrogen - are subjected to heat in a hot wall reactor, the reaction mixture is cooled down or allowed to cool down and the reaction product is separated from the gaseous substances in the form of a powder, - wherein the proportion of silane is between 0.1 and 90 wt.%, with respect to the sum of silane, doping material, hydrogen and inert gases, and wherein the proportion of hydrogen, with respect to the sum of hydrogen, silane, inert gas and optionally doping material is in the range 1 mol.% to 96 mol.%.
  • a wall-heated hot wall reactor may be used, wherein the hot wall reactor has a size such that as complete as possible conversion of the feedstock and optionally of doping material is achieved.
  • the residence time in the hot wall reactor is between 0.1 s and 2 s.
  • the maximum temperature in the hot wall reactor is preferably chosen in such a way that it does not exceed 1000°C.
  • Cooling the reaction mixture may be performed, for example, by external wall-cooling of the reactor or by the introduction of an inert gas in a quenching process.
  • a silane in the context of the invention may be a silicon- containing compound which provides silicon, hydrogen, nitrogen and/or halogens under the conditions of reaction.
  • SiH 4 , Si 2 H 6 , ClSiH 3 , Cl 2 SiH 2 , Cl 3 SiH and/or SiCl 4 may preferably used, wherein SiH 4 is particularly preferred.
  • hydrogen-containing compounds of phosphorus, arsenic, antimony, bismuth, boron, aluminium, gallium, indium, thallium, europium, erbium, cerium, praseodymium, neodymium, samarium, gadolinium, terbium, dysprosium, holmium, thulium, ytterbium, lutetium, lithium, germanium, iron, ruthenium, osmium, cobalt, rhodium, iridium, nickel, palladium, platinum, copper, silver, gold, zinc can be used.
  • Diborane and phosphane or substituted phosphanes such as tBuPH 2 , tBu 3 P, tBuPh 2 P and trismethyla inophosphane ((CH 3 ) 2 N) 3 P are particularly preferred.
  • phosphane or substituted phosphanes such as tBuPH 2 , tBu 3 P, tBuPh 2 P and trismethyla inophosphane ((CH 3 ) 2 N) 3 P are particularly preferred.
  • lithium in the case of lithium as a doping component, it has proven most beneficial to use the metal lithium or lithium amide LiNH 2 as the doping material .
  • Mainly nitrogen, helium, neon or argon may be used as an inert gas, wherein argon is particularly preferred.
  • the invention also provides use of the powder according to the invention to produce electronic components, electronic circuits and electrically active fillers.
  • the silicon powder according to the invention is free of amorphous constituents and has a high BET surface area.
  • the process according to the invention does not lead to the deposition of silicon on the reactor wall, as is described in the prior art. Furthermore, the process according to the invention enables the production of doped silicon powder.
  • the BET surface area is determined in accordance with DIN 66131.
  • the degree of doping is determined using glow discharge mass spectrometry (GDMS) .
  • the hydrogen loading is determined using " " " ⁇ -MAS-NMR spectroscopy.
  • a tube with a length of 200 cm and a diameter of 6 cm is used as a hot wall reactor. It consists of quartz glass or Si/SiC with a quartz glass liner. The tube is heated to 1000 °C externally using resistance heating over a length of 100 cm.
  • the pressure in the reactor is 1080 mbar.
  • the powdered product is separated from gaseous substances in a downstream filter unit.
  • the powder obtained has a BET surface area of 20 m 2 /g.
  • Figure 3 shows the X-ray diffraction diagram for silicon powder . Examples 2 to 6 are performed in the same way as example 1, but the parameters are modified. The parameters are given in table 1. Table 1: Process parameters and physico-chemical values of the silicon powders

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Nanotechnology (AREA)
  • Manufacturing & Machinery (AREA)
  • Silicon Compounds (AREA)
  • Catalysts (AREA)
  • Crystals, And After-Treatments Of Crystals (AREA)

Abstract

Aggregated crystalline silicon powder with a BET surface area of 20 to 150 m2/g. It is prepared by subjecting at least one vaporous or gaseous silane and optionally at least one vaporous or gaseous doping material, an inert gas and hydrogen to heat in a hot wall reactor, cooling the reaction mixture or allowing the reaction mixture to cool and separating the product from gaseous substances in the form of a powder, wherein the proportion of silane is between 0.1 and 90 wt.%, with respect to the sum of silane, doping material, hydrogen and inert gases, and wherein the proportion of hydrogen, with respect to the sum of hydrogen, silane, inert gas and doping material, is in the range 1 mol.% to 96 mol.%. It can be used to produce electronic components.

Description

Nanoscale crystalline silicon powder
The invention provides a nanoscale crystalline silicon powder and the preparation and use thereof .
It is known that an aggregated nanoscale silicon powder can be prepared in a hot wall reactor (Roth et al . , Chem. Eng. Technol. 24 (2001), 3). The disadvantage of this process has proven to be that the desired crystalline silicon is produced along with amorphous silicon which is formed by the reaction of silane at the hot reactor walls. In addition, the crystalline silicon has a low BET surface area of less than 20 m2/g and thus is generally too coarse for electronic applications.
Furthermore, Roth et al . do not disclose a process in which doped' silicon powders are obtained. Such doped silicon powders, with their semiconductor properties, are very important in the electronics industry. Furthermςre, it is a disadvantage that silicon powder is deposited on the reactor walls and acts as a thermal insulator. This changes the temperature profile in the reactor and thus also changes the properties of the silicon powder.
The object of the invention is the provision of a silicon powder which avoids the disadvantages of the prior art. In particular, the silicon powder should be one with a uniform modification.
The invention is also intended to provide a process by which this powder can be prepared on an industrial scale in an economically viable manner.
The invention provides an aggregated crystalline silicon powder with a BET surface area of 20 to 150 m/g. In a preferred embodiment, the silicon powder according to the invention may have a BET surface area of 40 to 120 m2/g.
The expression aggregated is understood to mean that the spherical or largely spherical particles which are initially formed in the reaction coalesce to form aggregates during the course of further reaction. The extent of growth may be affected by the process parameters. These aggregates may form agglomerates during the course of further reaction. In contrast to aggregates, which generally cannot or can only partly be broken down into the primary particles, agglomerates form only a loose association of aggregates which can easily be broken down into the aggregates .
The expression crystalline is understood to mean that at least 90% of the powder is crystalline. This degree of crystallinity can be determined by comparing the intensities of the [111], [220] and [311] signals of the powder according to the invention with those of a silicon powder of known crystallinity and crystallite size.
In the context of the invention, a silicon powder with a degree of crystallinity of at least 95%, particularly preferably one with at least 98% crystallinity, is preferred. The evaluation of TEM images and the counting of primary particles which exhibit lattice lines, as a feature of the crystalline state, is suitable for determining this degree of crystallisation.
Furthermore, the silicon powder according to the invention may be doped. The doping components may be phosphorus, arsenic, antimony, bismuth, boron, aluminium, gallium, indium, thallium, europium, erbium, cerium, praseodymium, neodymium, samarium, gadolinium, terbium, dysprosium, holmium, thulium, lutetium, lithium, ytterbium, germanium, iron, ruthenium, osmium, cobalt, rhodium, iridium, nickel, palladium, platinum, copper, silver, gold or zinc.
Particularly preferred, especially when used as a semiconductor in electronic components, the doping components may be the elements phosphorus, arsenic, antimony, bismuth, boron, aluminium, gallium, indium, thallium, europium, erbium, cerium, praseodymium, neodymium, samarium, gadolinium, terbium, dysprosium, holmium, thulium, ytterbium, lutetium. The proportion of these present in silicon powder according to the invention may be up to 1 wt.%. In general, a silicon powder is required in which the doping component is present in the pp or even the ppb range. A range of 1013 to 1015 atoms of doping component per cm3 is preferred. Furthermore, it is possible for silicon powder according to the invention to contain lithium as a doping component. The proportion of lithium present in the silicon powder may be up to 53 wt.%. Silicon powder with up to 20 to 40 wt.% of lithium may be particularly preferred. ' Similarly, silicon powder according to the invention may contain germanium as a doping component. The proportion of germanium present in the silicon powder may be up to 40 wt.%. Silicon powder with up to 10 to 30 wt.% of germanium may be particularly preferred. Finally, the elements iron, ruthenium, osmium, cobalt, rhodium, iridium, nickel, palladium, platinum, copper, silver, gold, zinc may also be doping components in the silicon powder. The proportion of these present may be up to 5 wt.% of the silicon powder. The doping components may be uniformly distributed in the powder or they may be enriched or intercalated in the shell or the core of the primary particles. The doping components may preferably be incorporated at silicon lattice sites. This depends substantially on the type of doping material and on reaction management.
A doping component in the context of the invention is understood to be the element present in the powder according to the invention. A doping material is understood to be the compound used in the process in order to obtain the doping component .
The silicon powder according to the invention may also have a hydrogen loading of up to 10 mol.%, wherein a range of 1 to 5 mol.% is particularly preferred. NMR spectroscopic methods such as, for example, 1H-MAS-NMR spectroscopy or IR spectroscopy are suitable for determining this.
The invention also provides a process for preparing the silicon powder according to the invention, characterised in that at least one vaporous or gaseous silane and optionally at least one vaporous or gaseous doping material, an inert gas and hydrogen - are subjected to heat in a hot wall reactor, the reaction mixture is cooled down or allowed to cool down and the reaction product is separated from the gaseous substances in the form of a powder, - wherein the proportion of silane is between 0.1 and 90 wt.%, with respect to the sum of silane, doping material, hydrogen and inert gases, and wherein the proportion of hydrogen, with respect to the sum of hydrogen, silane, inert gas and optionally doping material is in the range 1 mol.% to 96 mol.%. Particularly advantageously, a wall-heated hot wall reactor may be used, wherein the hot wall reactor has a size such that as complete as possible conversion of the feedstock and optionally of doping material is achieved. In general the residence time in the hot wall reactor is between 0.1 s and 2 s. The maximum temperature in the hot wall reactor is preferably chosen in such a way that it does not exceed 1000°C.
Cooling the reaction mixture may be performed, for example, by external wall-cooling of the reactor or by the introduction of an inert gas in a quenching process.
A silane in the context of the invention may be a silicon- containing compound which provides silicon, hydrogen, nitrogen and/or halogens under the conditions of reaction. SiH4, Si2H6, ClSiH3, Cl2SiH2, Cl3SiH and/or SiCl4 may preferably used, wherein SiH4 is particularly preferred. In addition, it is also possible to use N(SiH3)3, HN(SiH3)2, H2N(SiH3), (H3Si)2 N(SiH3)2, (H3Si) NH H (SiH3) , H2NN(SiH3)2.
Preferably, hydrogen-containing compounds of phosphorus, arsenic, antimony, bismuth, boron, aluminium, gallium, indium, thallium, europium, erbium, cerium, praseodymium, neodymium, samarium, gadolinium, terbium, dysprosium, holmium, thulium, ytterbium, lutetium, lithium, germanium, iron, ruthenium, osmium, cobalt, rhodium, iridium, nickel, palladium, platinum, copper, silver, gold, zinc can be used. Diborane and phosphane or substituted phosphanes such as tBuPH2, tBu3P, tBuPh2P and trismethyla inophosphane ((CH3)2N)3P are particularly preferred. In the case of lithium as a doping component, it has proven most beneficial to use the metal lithium or lithium amide LiNH2 as the doping material . Mainly nitrogen, helium, neon or argon may be used as an inert gas, wherein argon is particularly preferred. The invention also provides use of the powder according to the invention to produce electronic components, electronic circuits and electrically active fillers.
The silicon powder according to the invention is free of amorphous constituents and has a high BET surface area. The process according to the invention does not lead to the deposition of silicon on the reactor wall, as is described in the prior art. Furthermore, the process according to the invention enables the production of doped silicon powder.
Examples :
Analytical techniques: The BET surface area is determined in accordance with DIN 66131. The degree of doping is determined using glow discharge mass spectrometry (GDMS) . The hydrogen loading is determined using ""Ή-MAS-NMR spectroscopy.
Apparatus used;
A tube with a length of 200 cm and a diameter of 6 cm is used as a hot wall reactor. It consists of quartz glass or Si/SiC with a quartz glass liner. The tube is heated to 1000 °C externally using resistance heating over a length of 100 cm.
A SiH4/argon mixture (mixture 1) of 1000 seem of silane (standard centimetre cube per minute; 1 seem = 1 cm3 of gas per minute with reference to 0°C and atmospheric pressure) and 3000 seem of argon and a mixture of argon and hydrogen (mixture 2), 5000 seem of each, are supplied from above the hot wall reactor via a two-fluid nozzle. The pressure in the reactor is 1080 mbar. The powdered product is separated from gaseous substances in a downstream filter unit.
The powder obtained has a BET surface area of 20 m2/g. Figure 3 shows the X-ray diffraction diagram for silicon powder . Examples 2 to 6 are performed in the same way as example 1, but the parameters are modified. The parameters are given in table 1. Table 1: Process parameters and physico-chemical values of the silicon powders
Figure imgf000009_0001

Claims

Claims :
1. Aggregated crystalline silicon powder, characterised in that it has a BET surface area of 20 to 150 m2/g.
2. Aggregated crystalline silicon powder according to Claim 1, characterised in that the BET surface area is between, 40 and 120 m2/g.
3. Aggregated crystalline silicon powder according to Claims 1 or 2 , characterised in that it is doped with phosphorus, arsenic, antimony, bismuth, boron, aluminium, gallium, indium, thallium, europium, erbium, cerium, praseodymium, neodymium, samarium, gadolinium, terbium, dysprosium, holmium, thulium, lutetium, lithium, ytterbium, germanium, iron, ruthenium, osmium, cobalt, rhodium, iridium, nickel, palladium, platinum, copper, silver, gold, zinc.
4. Aggregated crystalline silicon powder according to Claim 3, characterised in that the proportion of doping components phosphorus, arsenic, antimony, bismuth, boron, aluminium, gallium, indium, thallium, europium, erbium, cerium, praseodymium, neodymium, samarium, gadolinium, terbium, dysprosium, holmium, thulium, ytterbium, lutetium is up to 1 wt.%.
5. Aggregated crystalline silicon powder according to Claim 3, characterised in that the proportion of doping component lithium is up to 53 wt.%.
6. Aggregated crystalline silicon powder according to Claim 3, characterised in that the proportion of doping component germanium is up to 40 wt.%.
7. Aggregated crystalline silicon powder according to Claim 3, characterised in that the proportion of doping components iron, ruthenium, osmium, cobalt, rhodium, iridium, nickel, palladium, platinum, copper, silver, gold and zinc is up to 5 wt.%.
8. Aggregated crystalline silicon powder according to Claims 1 to 7 , characterised in that it has a hydrogen loading of up to 10 mol.%.
9. A process for preparing the aggregated crystalline silicon powder according to Claims 1 to 8, characterised in that at least one vaporous or gaseous silane and optionally at least one vaporous or gaseous doping material, an inert gas and hydrogen are subjected to heat in a hot wall reactor, the reaction mixture is cooled down or allowed to cool down and the reaction product is separated from the gaseous substances in the form of a powder, | wherein the proportion of silane is between 0.1 and 90 wt.%, with respect to the sum of silane, doping material, hydrogen and inert gases and wherein the proportion of hydrogen, with respect to the sum of hydrogen, silane, inert gas and doping material is in the range 1 mol.% to 96 mol.%.
10. A process according to Claim 9, characterised in that the silane is chosen from the group of compounds SiH4, Si2H6, ClSiH3, Cl2SiH2, Cl3SiH and/or SiCl4.
11. A process according to Claim 9 or 10, characterised in that the silane to be used is chosen from the group of compounds N(SiH3) 3, HN(SiH3)2, H2N(SiH3), (H3Si) 2NN(SiH3) 2, (H3Si)NHNH(SiH3) , H2NN(SiH3)2.
12. A process according to Claims 9 to 11, characterised in that the doping material is chosen from the group of hydrogen-containing compounds of phosphorus, arsenic, antimony, bismuth, boron, aluminium, gallium, indium, thallium, europium, erbium, cerium, praseodymium, neodymium, samarium, gadolinium, terbium, dysprosium, holmium, thulium, ytterbium, lutetium, lithium, germanium, iron, ruthenium, osmium, cobalt, rhodium, iridium, nickel, palladium, platinum, copper, silver, gold, zinc.
13. A process according to Claims 9 to 12, characterised in that the doping material is lithium metal or lithium amide (LiNH2) .
14. A process according to Claims 9 to 13, characterised in that nitrogen, helium, neon, argon are used as inert gases.
15. Use of the silicon powder according to Claims 1 to 8 to produce electronic components, electronic circuits and electrically active fillers.
PCT/EP2004/012890 2003-11-19 2004-11-13 Nanoscale crystalline silicon powder WO2005049492A1 (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
EP04797876A EP1685066B1 (en) 2003-11-19 2004-11-13 Nanoscale crystalline silicon powder
AT04797876T ATE517059T1 (en) 2003-11-19 2004-11-13 NANOSCALE CRYSTALLINE SILICON POWDER
JP2006540274A JP4607122B2 (en) 2003-11-19 2004-11-13 Nanoscale crystalline silicon powder
UAA200606737A UA87672C2 (en) 2003-11-19 2004-11-13 Aggregated crystalline silicon powder, process for preparation and use thereof
US10/579,460 US7776304B2 (en) 2003-11-19 2004-11-13 Nanoscale crystalline silicon powder
IL175701A IL175701A (en) 2003-11-19 2006-05-17 Process for preparing aggregate crystalline silicon powder
US12/759,346 US8043593B2 (en) 2003-11-19 2010-04-13 Nanoscale crystalline silicon powder
US12/829,464 US7927570B2 (en) 2003-11-19 2010-07-02 Nanoscale crystalline silicon powder

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10353995A DE10353995A1 (en) 2003-11-19 2003-11-19 Nanoscale, crystalline silicon powder
DE10353995.6 2003-11-19

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US12/759,346 Division US8043593B2 (en) 2003-11-19 2010-04-13 Nanoscale crystalline silicon powder
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