US3152022A - Epitaxial deposition on the surface of a freshly grown dendrite - Google Patents
Epitaxial deposition on the surface of a freshly grown dendrite Download PDFInfo
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- US3152022A US3152022A US197678A US19767862A US3152022A US 3152022 A US3152022 A US 3152022A US 197678 A US197678 A US 197678A US 19767862 A US19767862 A US 19767862A US 3152022 A US3152022 A US 3152022A
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- dendrite
- growth
- melt
- crystal
- epitaxial
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- 210000001787 dendrite Anatomy 0.000 title claims description 17
- 230000008021 deposition Effects 0.000 title description 12
- 239000004065 semiconductor Substances 0.000 claims description 17
- 238000000151 deposition Methods 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 11
- 239000000155 melt Substances 0.000 claims description 10
- 239000000758 substrate Substances 0.000 claims description 10
- 239000013078 crystal Substances 0.000 description 23
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000007789 gas Substances 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 229910006113 GeCl4 Inorganic materials 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229910052732 germanium Inorganic materials 0.000 description 3
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- IEXRMSFAVATTJX-UHFFFAOYSA-N tetrachlorogermane Chemical compound Cl[Ge](Cl)(Cl)Cl IEXRMSFAVATTJX-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 230000006911 nucleation Effects 0.000 description 2
- 238000010899 nucleation Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 1
- 241000845077 Iare Species 0.000 description 1
- 102100035031 Palladin Human genes 0.000 description 1
- 101710128215 Palladin Proteins 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 238000010420 art technique Methods 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 230000003467 diminishing effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000000407 epitaxy Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- WPYVAWXEWQSOGY-UHFFFAOYSA-N indium antimonide Chemical compound [Sb]#[In] WPYVAWXEWQSOGY-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- WGPCGCOKHWGKJJ-UHFFFAOYSA-N sulfanylidenezinc Chemical compound [Zn]=S WGPCGCOKHWGKJJ-UHFFFAOYSA-N 0.000 description 1
- 238000004781 supercooling Methods 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
Images
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
- C30B15/00—Single-crystal growth by pulling from a melt, e.g. Czochralski method
- C30B15/30—Mechanisms for rotating or moving either the melt or the crystal
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S117/00—Single-crystal, oriented-crystal, and epitaxy growth processes; non-coating apparatus therefor
- Y10S117/903—Dendrite or web or cage technique
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S148/00—Metal treatment
- Y10S148/021—Continuous process
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S148/00—Metal treatment
- Y10S148/025—Deposition multi-step
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S148/00—Metal treatment
- Y10S148/15—Silicon on sapphire SOS
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S438/00—Semiconductor device manufacturing: process
- Y10S438/913—Diverse treatments performed in unitary chamber
Definitions
- This invention concerns epitaxial deposition of semiconductors and, more particularly, epitaxial growth on semiconductor substrates prepared by dendritic growth.
- Typical prior art techniques for the growth of epitaxial films on semiconductor substrates include elaborate and costly techniques for surface preparation preparatory to deposition.
- the usual slice cut from crystal ingot prepared in the ordinary fashion, such as by zone refining, possesses a surface which is unfit for epitaxial growth.
- the surface must first be lapped to remove the large surface discontinuities resulting from the cutting operation. This step may involve electromechanical or electrolytic polishing with or without mechanical abrading, the latter oftenA involving a stepwise operation with abrasives of diminishing size.
- the surface is then washed, dried, and etched to remove strains introduced into the crystal surface during the abrading step. Another rinse follows with a final drying of the surface. All of these operations are time consuming and costly with the added danger of fracturing the crystal during abrading, or of incomplete or imperfect surface preparation ultimately resulting in a defective device unit.
- the invention consists essentially of preparing a semiconductor crystal by the technique of dendritic growth and, as 'a successive step in the same operation, depositing an epitaxial film on the freshly grown substrate.
- the apparatus of the figure consists basically of a reaction chamber iitted for the introduction of the necessary gaseous components for the process and provided with 'appropriate heating means.
- the reaction vessel itself is a long vertical quartz tube having approximate dimensions of 4 inches (diameter) by 3 feet (length).
- the tube contains a graphite crucible 11, filled with charge material for the melt from which the dendrite is pulled. ⁇
- an electrically conductive pulling shaft 12 Depending from the top of the tube is an electrically conductive pulling shaft 12, sealed with O-ring seal 13.
- the shaft terminates in a graphite 'tip 14 which serves as the seed holder.
- an R.F. heating coil contained in a container 16, for water-cooling the coil.
- An exhaust tube 17 is provided as shown.
- the gas system here provides a means for evacuating the reaction chamber, flushing it with nitrogen and introducing a hydrogen atmosphere for pulling the crystal. Provision is made to alternatively direct the hydrogen through a source of semiconductor for the epitaxial deposition.
- purified hydrogen and nitrogen are introduced at inlets 20 and 21 system is designed to provide a source material for epitaxial growth.
- the first stage of the epitaxy so ⁇ system is a purifying operation which consists of pas the H2 gas through tube 30 containing palladin VAlundum. The gas is then directed through a li nitrogen trap 31 which includes container 32 for liquid coolant.
- the purified gas leaving the trap is reoted through thepline 33 into the saturator 34 w1 the hydrogen is saturated with a semiconductor v: compound.
- the growth layer i be germanium so that GeCl4 is chosen as the source m rial contained in the saturator.
- the saturator is pended in a cold bath 35 contained in beaker 36. cold bath is appropriately ethylene glycol and Dry which maintains the GeCl4 at 40 C.
- the inlet outlet to the saturator Iare controlled by valves 37 3S. The outlet leads into the reaction vessel.
- the heating circuit shown was used to provide the l necessary for the epitaxial deposition. It is connecte that the current flow is through the dendrite after dendrite -is pulled. For this purpose it is necessary the dendrite not be withdrawn from the melt after I ing.
- the current flow from source 39 is adjusted so the Joule heat in the dendrite maintains the proper t perature for the epitaxial deposition.
- the conduccrucible 11 and seed holder 14 are included for this 1 pose.
- the system was ushed with nitrogen and a hydrc atmosphere was introduced for the growth operat
- the Crucible 11 was charged with 60 grams of high pot zone-refined germanium doped with arsenic to a resisti of 1.3 ohm-cm.
- the seed crystal, the form of wl dictates whether the growth is polyhedral (slow) dendritic (fast), necessarily contains 'at least two t planes, for dendritic growth.
- twin plane presents a groove at the twin boundary al which nucleation and growth proceed rapidly.
- twin planes If c one twin plane is present the rapid growth is soon tel nated because the ridges of the hexagonal platelet groi the expense of the grooves until the crystal is boun l wholly by ridges. Growth along aridge is slow sinc relies on surface nucleation and thus grows by polyhe or slow growth. Two twin planes present a continuoi available groove for continuous fast growth.
- the seed crystal contained twin planes parallel to (111) having external faces pa lel to (111).
- the vertical direction toward the m ⁇ was [ll].
- the temperature of the melt which is'ne sarily supercooled to a practical operating value b3 least 3 C., was adjusted to give a stationary solid-lic interface and then reduced about 10 C. as measured a thermocouple 1/2' cm. below the surface.
- the cry was then withdrawn ata rate of 0.5 cm./ sec.
- the de; of supercooling bears a linear relation to the growth 1 so that highly supercooled melts are preferred from standpoint.
- a practical maximum in the degree. of su] cooling useful for this invention is 20 C.
- the seed crystal may, of course, itself be a dend or it may be cut from a polyhedrally grown crystal. either case it must contain two twin planes.
- the of the seed was approximately 5 cm. x 3 mm. x .1 n
- the dendrite substrate has its long dimension in le (111) plane.
- the crystal was n-type as expected and ad a resistivity of approximately 1.3 ohm-cm.
- the film :tained in the second or epitaxial growth step was iamined by angle lapping and etching. It was found to a epitaxial in nature with a thickness of 8 microns. 'ne film in this embodiment was also n-type. However, f proper doping p-type films can also be obtained ing the procedures of this invention. As will be appreciated to those skilled in the art this vention is directed to epitaxial growth on a freshly epared dendritically grown surface.
- III-V compounds are of increasing importance semiconductor device development.
- III-V compounds particular interest are GaAs, GaP and InSb.
- Epitaxial ns on dissimilar semiconducting substrates ,and parularly heterojunctions may also be grown according to techniques of this invention.
- the conditions for a epitaxial depositions according to this invention may the same as those known in the art for deposition on linary polyhedrally grown semiconductor substrates.
- dendritic growth are known the art, the term is defined here as simply rapid crystal growth, i.e., at least 0.01 cm./sec. from a supercooled melt on a seed crystal containing at least two parallel coherent twin planes. The growth occurs along a (111) crystal plane and may be of unlimited length. The latter fact suggests a continuous processing operation according to the present invention.
- a method for growing an epitaxal semiconductor film on a semiconductor substrate which comprises suspending a seed crystal in a melt of the semiconductor desired as the substrate, said melt being supercooled at least 3 C., the seed crystal having at least .two parallel twin planes, pulling the seed crystal from the melt at a ratev of at least 0.01 ern/sec. in a direction parallel to the twin planes to form a dendrite and, as a successive step in the same process and in the same apparatus vapor-depositing an epitaxially grown semiconductor film on the surface of the freshly formed dendrite.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Liquid Deposition Of Substances Of Which Semiconductor Devices Are Composed (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
Description
Oct. s, 1964 CHRISTENSEN ETAL EPITAXIAL. DEPOSITION 0N THE SURFACE OF A FRESHLY GROWN DENDRITE Filed lay 25, 1962 POIYE R SOURCE l AMP) H. CHR/STENSEN Nm/Tons: R. s. WAGNER ATTORNEY r anx-Lamm.;
United States Patent Ohice 3,l52,(l Patented Oct. 6, l!
3,152,022 EPITAXIAL DEPOSITION ON THE SURFACE OF A FRESHLY GROWN DENDRITE Howard Christensen, Springeld, and Richard S. Wagner,
Basking Ridge, NJ., assignors to Bell Telephone Laboratories, Incorporated, New York, N.Y., a corporation of New York Filed May 25, 1962, Ser. No. 197,678 3 Claims. (Cl. 148-175) This invention concerns epitaxial deposition of semiconductors and, more particularly, epitaxial growth on semiconductor substrates prepared by dendritic growth.
Typical prior art techniques for the growth of epitaxial films on semiconductor substrates include elaborate and costly techniques for surface preparation preparatory to deposition. The usual slice cut from crystal ingot prepared in the ordinary fashion, such as by zone refining, possesses a surface which is unfit for epitaxial growth. The surface must first be lapped to remove the large surface discontinuities resulting from the cutting operation. This step may involve electromechanical or electrolytic polishing with or without mechanical abrading, the latter oftenA involving a stepwise operation with abrasives of diminishing size. The surface is then washed, dried, and etched to remove strains introduced into the crystal surface during the abrading step. Another rinse follows with a final drying of the surface. All of these operations are time consuming and costly with the added danger of fracturing the crystal during abrading, or of incomplete or imperfect surface preparation ultimately resulting in a defective device unit.
These diiiiculties are overcome by the teachings of this invention. The invention consists essentially of preparing a semiconductor crystal by the technique of dendritic growth and, as 'a successive step in the same operation, depositing an epitaxial film on the freshly grown substrate.
A more thorough understanding of the invention may be obtained with the following detailed embodiment taken in conjunction with the drawing in which the figure is a schematic representation of an Iappropriate apparatus useful n carrying forth the principal operation of this invention.
The apparatus of the figure consists basically of a reaction chamber iitted for the introduction of the necessary gaseous components for the process and provided with 'appropriate heating means. The reaction vessel itself is a long vertical quartz tube having approximate dimensions of 4 inches (diameter) by 3 feet (length). The tube contains a graphite crucible 11, filled with charge material for the melt from which the dendrite is pulled.`
Depending from the top of the tube is an electrically conductive pulling shaft 12, sealed with O-ring seal 13. The shaft terminates in a graphite 'tip 14 which serves as the seed holder. Surrounding the base portion of the quartz tube is an R.F. heating coil contained in a container 16, for water-cooling the coil. An exhaust tube 17 is provided as shown.
The gas system here provides a means for evacuating the reaction chamber, flushing it with nitrogen and introducing a hydrogen atmosphere for pulling the crystal. Provision is made to alternatively direct the hydrogen through a source of semiconductor for the epitaxial deposition. In the system shown in the figure purified hydrogen and nitrogen are introduced at inlets 20 and 21 system is designed to provide a source material for epitaxial growth. The first stage of the epitaxy so` system is a purifying operation which consists of pas the H2 gas through tube 30 containing palladin VAlundum. The gas is then directed through a li nitrogen trap 31 which includes container 32 for liquid coolant. The purified gas leaving the trap is reoted through thepline 33 into the saturator 34 w1 the hydrogen is saturated with a semiconductor v: compound. In this particular case the growth layer i be germanium so that GeCl4 is chosen as the source m rial contained in the saturator. The saturator is pended in a cold bath 35 contained in beaker 36. cold bath is appropriately ethylene glycol and Dry which maintains the GeCl4 at 40 C. The inlet outlet to the saturator Iare controlled by valves 37 3S. The outlet leads into the reaction vessel.
The heating circuit shown was used to provide the l necessary for the epitaxial deposition. It is connecte that the current flow is through the dendrite after dendrite -is pulled. For this purpose it is necessary the dendrite not be withdrawn from the melt after I ing. The current flow from source 39 is adjusted so the Joule heat in the dendrite maintains the proper t perature for the epitaxial deposition. The conduc Crucible 11 and seed holder 14 are included for this 1 pose.
Other heating arrangements such as a tunnel furr are, of course, suitable. The latter has the advantagl simple adaptability to continuous growth.
A specific operation using this apparatus is describa follows:
The system was ushed with nitrogen and a hydrc atmosphere was introduced for the growth operat The Crucible 11 was charged with 60 grams of high pui zone-refined germanium doped with arsenic to a resisti of 1.3 ohm-cm. The seed crystal, the form of wl dictates whether the growth is polyhedral (slow) dendritic (fast), necessarily contains 'at least two t planes, for dendritic growth. The presence of a cohe: twin plane presents a groove at the twin boundary al which nucleation and growth proceed rapidly. If c one twin plane is present the rapid growth is soon tel nated because the ridges of the hexagonal platelet groi the expense of the grooves until the crystal is boun l wholly by ridges. Growth along aridge is slow sinc relies on surface nucleation and thus grows by polyhe or slow growth. Two twin planes present a continuoi available groove for continuous fast growth.
In this embodiment the seed crystal contained twin planes parallel to (111) having external faces pa lel to (111). The vertical direction (toward the m` was [ll]. The temperature of the melt, which is'ne sarily supercooled to a practical operating value b3 least 3 C., was adjusted to give a stationary solid-lic interface and then reduced about 10 C. as measured a thermocouple 1/2' cm. below the surface. The cry was then withdrawn ata rate of 0.5 cm./ sec. The de; of supercooling bears a linear relation to the growth 1 so that highly supercooled melts are preferred from standpoint. A practical maximum in the degree. of su] cooling useful for this invention is 20 C.
The seed crystal may, of course, itself be a dend or it may be cut from a polyhedrally grown crystal. either case it must contain two twin planes. The of the seed was approximately 5 cm. x 3 mm. x .1 n
During the dendrite growth an atmosphere of hydro was maintained. The crystal was pulled to a length about 2 0". The melt was allowed to solidify with dendrite immersed. The heating circuit was turned and the current through the dendrite was adjusted approximately v. at 1 amp. The initial volt lust be substantially higher due to the difference in reistivity encountered as the crystal heats. This power :vel was found to produce the desired deposition temerature, 835 C., as measured on an optical pyrometer. `he hydrogen flow was diverted through the GeCl4 aturating system and adjusted to enter the chamber at cc./min. The epitaxial deposition continued for te-n linutes `after which the heating circuit was disconnected nd the gas ow returned to pure hydrogen. The dendrite 'as separated from the melt by using the R.F. heater to telt off the lower end. The system was flushed with itrogen and the sample was removed.
The dendrite substrate has its long dimension in le (111) plane. The crystal was n-type as expected and ad a resistivity of approximately 1.3 ohm-cm. The film :tained in the second or epitaxial growth step was iamined by angle lapping and etching. It was found to a epitaxial in nature with a thickness of 8 microns. 'ne film in this embodiment was also n-type. However, f proper doping p-type films can also be obtained ing the procedures of this invention. As will be appreciated to those skilled in the art this vention is directed to epitaxial growth on a freshly epared dendritically grown surface. Since this concept more or less physical in nature it is obvious that it is plicable to any semiconductor material. While silicon d germanium are currently of primary practical inest, the III-V compounds are of increasing importance semiconductor device development. III-V compounds particular interest are GaAs, GaP and InSb. Epitaxial ns on dissimilar semiconducting substrates ,and parularly heterojunctions may also be grown according to techniques of this invention. The conditions for a epitaxial depositions according to this invention may the same as those known in the art for deposition on linary polyhedrally grown semiconductor substrates. While the principles of dendritic growth are known the art, the term is defined here as simply rapid crystal growth, i.e., at least 0.01 cm./sec. from a supercooled melt on a seed crystal containing at least two parallel coherent twin planes. The growth occurs along a (111) crystal plane and may be of unlimited length. The latter fact suggests a continuous processing operation according to the present invention.
Various other modifications and extensions of this invention will become apparent to those skilled in the art. All such variations and deviations which basically rely on the teachings through which this invention has advanced the art are properly considered within the spirit and scope of this invention.
What is claimed is 1. A method for growing an epitaxal semiconductor film on a semiconductor substrate which comprises suspending a seed crystal in a melt of the semiconductor desired as the substrate, said melt being supercooled at least 3 C., the seed crystal having at least .two parallel twin planes, pulling the seed crystal from the melt at a ratev of at least 0.01 ern/sec. in a direction parallel to the twin planes to form a dendrite and, as a successive step in the same process and in the same apparatus vapor-depositing an epitaxially grown semiconductor film on the surface of the freshly formed dendrite.
2. The method of claim 1 wherein the seed crystal has a diamond cubic crystal structure.
3. The method of claim 1 wherein the seed crystal has a zinc blende crystal structure.
References Cited in the file of this patent UNITED STATES PATENTS 2,854,363 Seiler Sept. 30, 1958 3,031,403 Bennett Apr. 24, 1962 OTHER REFERENCES I.B.M. Technical Disclosure Bulletin, vol. 3, No. 2, July 1960, p. 45.
Claims (1)
1. A METHOD FOR GROWING AN EPITAXIAL SEMICONDUCTOR FILM ON A SEMICONDUCTOR SUBSTRATE WHICH COMPRISES SUSPENDING A SEED CRYSTAL IN A MELT OF THE SEMICONDUCTOR DESIRED AS THE SUBSTRATE, SAID MELT BEING SUPERCOOLED AT LEAST 3*C., THE SEED CRYSTAL HAVING AT LEAST TWO PARALLEL TWIN PLANES, PULLING THE SEED CRYSTAL FROM THE MELT AT A RATE OF AT LEAST 0.01 CM./SEC. IN A DIRECTION PARALLEL TO THE TWIN PLANES TO FORM A DENDRITE AND, AS A SUCCESSIVE STEP IN THE SAME PROCESS AND IN THE SAME APPARATUS VAPOR-DEPOSITING AN EPITAXIALLY GROWN SEMICONDUCTOR FILM ON THE SURFACE OF THE FRESHLY FORMED DENDRITE.
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US197678A US3152022A (en) | 1962-05-25 | 1962-05-25 | Epitaxial deposition on the surface of a freshly grown dendrite |
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US197678A US3152022A (en) | 1962-05-25 | 1962-05-25 | Epitaxial deposition on the surface of a freshly grown dendrite |
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Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3235418A (en) * | 1962-06-14 | 1966-02-15 | Siemens Ag | Method for producing crystalline layers of high-boiling substances from the gaseous phase |
US3268301A (en) * | 1962-12-03 | 1966-08-23 | Siemens Ag | Method of pulling a semiconductor crystal from a melt |
US3337379A (en) * | 1964-12-23 | 1967-08-22 | Sprague Electric Co | Method of making semiconductive devices by means of a carrier gas with impurities |
US3338761A (en) * | 1965-03-31 | 1967-08-29 | Texas Instruments Inc | Method and apparatus for making compound materials |
US3341376A (en) * | 1960-04-02 | 1967-09-12 | Siemens Ag | Method of producing crystalline semiconductor material on a dendritic substrate |
US3341358A (en) * | 1964-03-31 | 1967-09-12 | Arthur R Clawson | Fabrication of magnetoresistive semiconductor film devices |
US3344002A (en) * | 1961-11-24 | 1967-09-26 | Siemens Ag | Method of producing epitaxial layers on semiconductor monocrystals |
US3377182A (en) * | 1963-03-27 | 1968-04-09 | Siemens Ag | Method of producing monocrystalline semiconductor bodies |
US3459152A (en) * | 1964-08-28 | 1969-08-05 | Westinghouse Electric Corp | Apparatus for epitaxially producing a layer on a substrate |
US3473974A (en) * | 1967-02-14 | 1969-10-21 | Westinghouse Electric Corp | Utilization of trace impurities in the vapor growth of crystals |
EP0045191A1 (en) * | 1980-07-28 | 1982-02-03 | Monsanto Company | Process and apparatus for the production of semiconductor bodies |
US5057183A (en) * | 1988-12-08 | 1991-10-15 | Sharp Kabushiki Kaisha | Process for preparing epitaxial II-VI compound semiconductor |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2854363A (en) * | 1953-04-02 | 1958-09-30 | Int Standard Electric Corp | Method of producing semiconductor crystals containing p-n junctions |
US3031403A (en) * | 1958-08-28 | 1962-04-24 | Westinghouse Electric Corp | Process for producing crystals and the products thereof |
-
1962
- 1962-05-25 US US197678A patent/US3152022A/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2854363A (en) * | 1953-04-02 | 1958-09-30 | Int Standard Electric Corp | Method of producing semiconductor crystals containing p-n junctions |
US3031403A (en) * | 1958-08-28 | 1962-04-24 | Westinghouse Electric Corp | Process for producing crystals and the products thereof |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3341376A (en) * | 1960-04-02 | 1967-09-12 | Siemens Ag | Method of producing crystalline semiconductor material on a dendritic substrate |
US3344002A (en) * | 1961-11-24 | 1967-09-26 | Siemens Ag | Method of producing epitaxial layers on semiconductor monocrystals |
US3235418A (en) * | 1962-06-14 | 1966-02-15 | Siemens Ag | Method for producing crystalline layers of high-boiling substances from the gaseous phase |
US3268301A (en) * | 1962-12-03 | 1966-08-23 | Siemens Ag | Method of pulling a semiconductor crystal from a melt |
US3377182A (en) * | 1963-03-27 | 1968-04-09 | Siemens Ag | Method of producing monocrystalline semiconductor bodies |
US3341358A (en) * | 1964-03-31 | 1967-09-12 | Arthur R Clawson | Fabrication of magnetoresistive semiconductor film devices |
US3459152A (en) * | 1964-08-28 | 1969-08-05 | Westinghouse Electric Corp | Apparatus for epitaxially producing a layer on a substrate |
US3337379A (en) * | 1964-12-23 | 1967-08-22 | Sprague Electric Co | Method of making semiconductive devices by means of a carrier gas with impurities |
US3338761A (en) * | 1965-03-31 | 1967-08-29 | Texas Instruments Inc | Method and apparatus for making compound materials |
US3473974A (en) * | 1967-02-14 | 1969-10-21 | Westinghouse Electric Corp | Utilization of trace impurities in the vapor growth of crystals |
EP0045191A1 (en) * | 1980-07-28 | 1982-02-03 | Monsanto Company | Process and apparatus for the production of semiconductor bodies |
US5057183A (en) * | 1988-12-08 | 1991-10-15 | Sharp Kabushiki Kaisha | Process for preparing epitaxial II-VI compound semiconductor |
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