US3849205A - Enhancement of solid state recrystallization by induced nucleation - Google Patents
Enhancement of solid state recrystallization by induced nucleation Download PDFInfo
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- US3849205A US3849205A US00391110A US39111073A US3849205A US 3849205 A US3849205 A US 3849205A US 00391110 A US00391110 A US 00391110A US 39111073 A US39111073 A US 39111073A US 3849205 A US3849205 A US 3849205A
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- 239000007787 solid Substances 0.000 title claims abstract description 51
- 230000006911 nucleation Effects 0.000 title claims abstract description 12
- 238000010899 nucleation Methods 0.000 title claims abstract description 12
- 238000001953 recrystallisation Methods 0.000 title claims description 23
- 239000013078 crystal Substances 0.000 claims abstract description 71
- 239000000463 material Substances 0.000 claims abstract description 45
- 238000000034 method Methods 0.000 claims abstract description 38
- 239000007788 liquid Substances 0.000 claims abstract description 20
- 229910052793 cadmium Inorganic materials 0.000 claims abstract description 9
- 229910052753 mercury Inorganic materials 0.000 claims abstract description 9
- 230000000644 propagated effect Effects 0.000 claims abstract description 4
- 239000000203 mixture Substances 0.000 claims description 22
- 230000008018 melting Effects 0.000 claims description 14
- 238000002844 melting Methods 0.000 claims description 14
- 239000004065 semiconductor Substances 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 5
- 230000007423 decrease Effects 0.000 claims description 2
- 230000001902 propagating effect Effects 0.000 claims description 2
- 229910002058 ternary alloy Inorganic materials 0.000 abstract description 4
- 229910045601 alloy Inorganic materials 0.000 abstract description 3
- 239000000956 alloy Substances 0.000 abstract description 3
- 239000003708 ampul Substances 0.000 description 13
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 5
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000011343 solid material Substances 0.000 description 4
- 229910000661 Mercury cadmium telluride Inorganic materials 0.000 description 2
- MCMSPRNYOJJPIZ-UHFFFAOYSA-N cadmium;mercury;tellurium Chemical compound [Cd]=[Te]=[Hg] MCMSPRNYOJJPIZ-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000011344 liquid material Substances 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
- 229910052714 tellurium Inorganic materials 0.000 description 2
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 229910002056 binary alloy Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B1/00—Single-crystal growth directly from the solid state
- C30B1/02—Single-crystal growth directly from the solid state by thermal treatment, e.g. strain annealing
-
- 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
- C30B13/00—Single-crystal growth by zone-melting; Refining by zone-melting
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B29/00—Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
- C30B29/10—Inorganic compounds or compositions
- C30B29/46—Sulfur-, selenium- or tellurium-containing compounds
- C30B29/48—AIIBVI compounds wherein A is Zn, Cd or Hg, and B is S, Se or Te
-
- 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
- Y10S420/00—Alloys or metallic compositions
- Y10S420/903—Semiconductive
Definitions
- ABSTRACT A method of forming single crystal semiconducting alloys from polycrystalline material is disclosed.
- One end of a polycrystalline ingot of a ternary alloy such as (Hg, Cd)Te is melted to cause some crystal growth from the liquid at the liquid solid interface.
- the crystal growth forms a seed or nucleation site.
- the crystal structure is then propagated through the rest of the ingot by any suitable solid state crystal growth technique.
- Mercury cadmium telluride is a ternary alloy which is often described as a pseudo-binary alloy since the mercury and cadmium behave as though they were only one element in combination with the tellurium.
- This alloy is a highly useful semiconducting material for the manufacture of electromagnetic radiation detectors.
- the intrinsic band gap of the material varies with i the relative amounts of mercury and cadmium present.
- the detectable wavelength of the devices fabricated therefrom can be varied over a considerable range.
- Several methods have been developed for production of homogeneous ingots of this material having a predetermined composition, such as that disclosed in U.S. Pat. No. 3,656,944.
- (Hg,Cd)Te material which is to function as a detector be single crystal.
- a majority of the ingots presently produced are polycrystalline.
- the use of a Bridgman furnace to produce single crystal from a polycrystalline ingot is discussed in U.S. Pat. No. 3,656,944. This method generates a gradient in the relative mercury and cadmium content from one end of the ingot to the other due to slow melting and refreezing. The result is that only a small portion of the ingot will be of the desired composition even if the entire ingot is a single crystal.
- .It is also an object of the present invention to provide a process for enhancement of solid state recrystallization by formation of a single crystal nucleation site.
- this invention consists of the steps of melting a small portion of one end of an ingot of poly crystalline (Hg,Cd)Te to initiate crystal growth from the liquid at the liquid-solid interface and then causing the single crystal structure to propagate through the rest of the ingot by solid state recrystallization.
- the small amount of crystal growth at the liquid-solid interface acts as a nucleation site for the solid state recrystallization.
- FIG. 1 is a cross-sectional view of a zone heating furnace with an ampoule containing an ingot of (Hg,Cd)Te in place;
- FIG. 2 is an exploded view of the ampoule in FIG. 1;
- FIG. 3 is a graph representing a temperature gradient maintained in the furnace of FIG. 1.
- a conventional electrically powered resistance-heated zone furnace is composed of an alumina wall 10 which defines a cylindrical chamber and heating elements 12. Positioned within the chamber is a quartz ampoule 14 containing an ingot of polycrystalline homogeneous (Hg,Cd)Te of the desired composition. The ingot is shown with a small portion 16 in liquid state, a small slush region 17, and the remainder 18 in solid state.
- Hg,Cd polycrystalline homogeneous
- the ampoule 14 with the solid ingot is placed in the furnace and a temperature gradient estab lished according to FIG. 3.
- the ampoule is positioned such that only a small portion 16 of the (Hg,Cd)Te material is at a temperature above its melting point.
- the greater portion 18 of the ingot remains in solid state. Since the material was homogeneous when placed in the furnace a region 17 of slush material, that is a mixture of liquid and solid material, will form between the liquid and solid state regions. Mass transfer from the liquid portion 16 to the slush region 17 will change the composition of the material at the edge 20 of the solid material. The change will raise the melting point of this region causing it to freeze and form single crystal material at the interface 20.
- This thin region of single crystal (Hg,Cd)Te grown 7 from the liquid forms a nucleus or seed at one end of point, for a period of time.
- the difference in free energy of the single crystal nucleus and the rest of the ingot establishes a driving force which allows the single crystal structure to propagate through the solid material 18.
- Another method allows the entire process to be carried out with a single furnace setup and increases the speed of the solid state recrystallization. This technique is to leave the ampoule in the furnace as shown in HQ.
- regions 16 and 17 of the ingot were melted in the nucleation step, mass transfer occurred causing the relative concentrations of Hg and Cd to vary through these regions. Therefore even if single crystal structure is formed in regions 16 and 17, they will be of little value. Region 18 remained solid through the process preventing the occurrence of any mass transfer. The single crystal material formed from region 18 will therefore have the same composition as the original ingot.
- the polycrystalline ingot was prepared according to U.S. Pat. No. 3,656,494 as follows. An approximately 20 cm long quartz ampoule having an inside diameter of mm and outside diameter of 16 mm was cleaned in a conventional manner. The ampoule was then loaded with 38.3795 grams of mercury, 5.7165 grams of cadmium, and 30.9040 grams of tellurium. The ampoule was then sealed and reacted overnight at 800C. The ampoule was then oil quenched.
- the ingot thus formed was approximately 12 centimeters long and had a uniform composition of Hg Cd Te
- the ingot was left in the ampoule and placed in a 3 zone furnace with the thermal profile illustrated in FIG. 3.
- the ampoule was positioned so that approximately 2 centimeters of the ingot was at a temperature above the melting point of this composi tion material. These conditions were maintained for 21 days.
- the ampoule was then removed from the furnace and cooled and the ingot was removed from the am poule. Upon inspection all the material which remained solid throughout the process was found to be single crystal and homogeneous with the same composition as the originally prepared ingot.
- a method for enhancement of solid state recrystallization of a polycrystalline ternary semiconductor compound consisting of the step of melting a portion of a polycrystalline ternary semiconductor compound ingot and allowing single crystal growth from the liquid to occur at the liquid-solid interface whereby a single crystal mucleus is formed at the liquid-solid interface.
- a method for enhancement of solid state recrystallization of polycrystalline (Hg,Cd)Te consisting of the step of melting a small .portion of a polycrystalline (Hg,Cd)Te ingot and allowing single crystal growth from the liquid to occur at the liquid-solid interface whereby a single crystal nucleus is formed at the liquidsolid interface.
- a process for forming single crystal (Hg,Cd)Te material from polycrystalline (Hg,Cd)Te material consisting of the steps of creating a nucleus of single crystal material by melting a small portion of a polycrystalline (Hg,Cd)Te ingot whereby single crystal growth occurs at the liquid solid interface and propagating the crystal structrue through the rest of the ingot by solid state recrystallization.
- a process according to claim 3 including the step of refreezing the melted portion of said ingot after the nucleus is formed at the liquid solid interface.
- solid state recrystallization step consists of maintaining the ingot at an elevated temperature below the melting point of the material whereby the single crystal structure propagates from the nucleus through the ingot.
- a process for forming single crystal (Hg,Cd)Te material from polycrystalline (Hg,Cd)Te consisting of the step of maintaining a temperature gradient throughout an ingot of polycrystalline (Hg,Cd)Te such that a small portion of said material is melted at the high temperature end and the temperature continuously decreases to the low temperature end whereby liquid state single crystal growth occurs at the liquidsolid interface forming a nucleation site from which the single crystal structure is propagated through the solid state portion of the ingot.
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- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
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- Inorganic Chemistry (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Liquid Deposition Of Substances Of Which Semiconductor Devices Are Composed (AREA)
Abstract
A method of forming single crystal semiconducting alloys from polycrystalline material is disclosed. One end of a polycrystalline ingot of a ternary alloy such as (Hg, Cd)Te is melted to cause some crystal growth from the liquid at the liquid-solid interface. The crystal growth forms a seed or nucleation site. The crystal structure is then propagated through the rest of the ingot by any suitable solid state crystal growth technique.
Description
ilnite States Patent [1 1 Bran et a1.
[ 1 Nov. 19, 1974 ENHANCEMENT OF SOLID STATE RECRYSTALLIZATION BY INDUCED NUCLEATION [75] Inventors: Maurice J. Brau, Richardson;
Richard A. Reynolds, Dallas, both of Tex.
[73] Assignee: Texas Instruments Incorporated,
Dallas, Tex.
[22] Filed: Aug. 27, 1973 [21] App]. No.: 391,110
[52] US. Cl 148/l.6, 148/171, 148/172, 252/623 V, 423/508, 23/301 R, 75/169 [51] Int. Cl. B0lj 17/02, H011 3/20 [58] Field of Search 148/1.6', 252/623 V; 423/508; 23/301 R; 75/169, 65 ZM [5 6] References Cited UNITED STATES PATENTS 1,793,672 2/1931 Bridgman l48/1.6 UX
2,953,690 9/1960 Lawson et a1 75/169 X 3,468,363 9/1969 Parker et a1. 75/169 X 3,622,399 11/1971 Johson l48/1.6 3,656,944 4/1972 Brau 75/135 3,723,190 3/1973 Kruse et a1 148]].6 X
Primary ExaminerG. Ozaki Attorney, Agent, or Firm--Harold Levine; Rene E. Grossman; Alva H. Bandy [5 7] ABSTRACT A method of forming single crystal semiconducting alloys from polycrystalline material is disclosed. One end of a polycrystalline ingot of a ternary alloy such as (Hg, Cd)Te is melted to cause some crystal growth from the liquid at the liquid solid interface. The crystal growth forms a seed or nucleation site. The crystal structure is then propagated through the rest of the ingot by any suitable solid state crystal growth technique.
8 Claims, 3 Drawing Figures PATENTEL HUV 1 9 I974 nlll'l 73 cm IIII|IIY Fig l INGO'I LOCATION IO [5 20 v HEIGHT FROlVl- FURNACE BOTTOM INCHES ENHANCEMENT OF SOLID STATE RECRYSTALLIZATION BY INDUCED NUCLEATION This invention relates to the production of single crystal tenary semiconductor compounds and more particularly to mercury cadmium telluride ((Hg,Cd)Te) from polycrystalline material.
Mercury cadmium telluride is a ternary alloy which is often described as a pseudo-binary alloy since the mercury and cadmium behave as though they were only one element in combination with the tellurium. This alloy is a highly useful semiconducting material for the manufacture of electromagnetic radiation detectors. The intrinsic band gap of the material varies with i the relative amounts of mercury and cadmium present.
Accordingly, by varying the composition of the material, the detectable wavelength of the devices fabricated therefrom can be varied over a considerable range. Several methods have been developed for production of homogeneous ingots of this material having a predetermined composition, such as that disclosed in U.S. Pat. No. 3,656,944.
It is desirable that (Hg,Cd)Te material which is to function as a detector be single crystal. A majority of the ingots presently produced are polycrystalline. The use of a Bridgman furnace to produce single crystal from a polycrystalline ingot is discussed in U.S. Pat. No. 3,656,944. This method generates a gradient in the relative mercury and cadmium content from one end of the ingot to the other due to slow melting and refreezing. The result is that only a small portion of the ingot will be of the desired composition even if the entire ingot is a single crystal.
Another method for producing single crystal material from polycrystalline ingots is disclosed by T. C. Harman in the Solid State Research report of the Lincoln Laboratory MIT, 1970 Vol. 3, p. 2. This process involves melting a portion of a polycrystalline homogeneous ingot to form a slush region, that is a mixture of liq uid and solid material, between the liquid and solid regions. Mass transfer from the liquid to the slush changes the composition of the slush causing it to freeze and form single crystal material. This method produces single crystal homogeneous material in only a portion of the ingot. The composition of this single crystal portion is also different from the original composition.
Any process for forming single crystal (Hg,Cd)Te in which the material is melted and refrozen results in a change in composition of the material.
Several methods of solid state recrystallization, or annealing of polycrystalline materials are known in the art. Such a process is particularly useful in forming single crystals of ternary alloys such as (Hg,Cd)Te since the material remains solid and no compositional change occurs during crystal growth. Recrystallization generally causes an increase in the crystal grain size throughout the ingot. Growth of one or only a few crystals grains larger than the rest is often termed secondary recrystallization. This large grain growth is the goal when single crystal semiconductor material is needed. A nucleation site or seed is a region of single crystal material which will grow at the expense of other crystal regions in an ingot, and this causes secondary recrystallization. Present recrystallization methods depend upon the natural occurrence of a nucleation site to cause single crystal growth through an ingot. The re sult is that most recrystallized ingots are not substantially single crystal.
Accordingly, it is an object of the present invention to provide a process for forming single crystal (Hg,Cd)Te material from substantially all of a polycrystalline ingot of (Hg,Cd)Te.
It is also an object of the present invention to provide a process for forming single crystal (Hg,Cd )Te material from polycrystalline (Hg,Cd)Te without changing the relative concentrations of mercury and cadmium.
.It is also an object of the present invention to provide a process for enhancement of solid state recrystallization by formation of a single crystal nucleation site.
Briefly stated, this invention consists of the steps of melting a small portion of one end of an ingot of poly crystalline (Hg,Cd)Te to initiate crystal growth from the liquid at the liquid-solid interface and then causing the single crystal structure to propagate through the rest of the ingot by solid state recrystallization. The small amount of crystal growth at the liquid-solid interface acts as a nucleation site for the solid state recrystallization.
Other objects and features of the invention will become more readily understood from the following dctailed description and appended claims when read in conjunction with the accompanying drawings, wherein:
FIG. 1 is a cross-sectional view of a zone heating furnace with an ampoule containing an ingot of (Hg,Cd)Te in place;
FIG. 2 is an exploded view of the ampoule in FIG. 1; and
FIG. 3 is a graph representing a temperature gradient maintained in the furnace of FIG. 1.
Referring to FIGS. 1 and 2, a conventional electrically powered resistance-heated zone furnace is composed of an alumina wall 10 which defines a cylindrical chamber and heating elements 12. Positioned within the chamber is a quartz ampoule 14 containing an ingot of polycrystalline homogeneous (Hg,Cd)Te of the desired composition. The ingot is shown with a small portion 16 in liquid state, a small slush region 17, and the remainder 18 in solid state.
In operation, the ampoule 14 with the solid ingot is placed in the furnace and a temperature gradient estab lished according to FIG. 3. The ampoule is positioned such that only a small portion 16 of the (Hg,Cd)Te material is at a temperature above its melting point. The greater portion 18 of the ingot remains in solid state. Since the material was homogeneous when placed in the furnace a region 17 of slush material, that is a mixture of liquid and solid material, will form between the liquid and solid state regions. Mass transfer from the liquid portion 16 to the slush region 17 will change the composition of the material at the edge 20 of the solid material. The change will raise the melting point of this region causing it to freeze and form single crystal material at the interface 20.
This thin region of single crystal (Hg,Cd)Te grown 7 from the liquid forms a nucleus or seed at one end of point, for a period of time. The difference in free energy of the single crystal nucleus and the rest of the ingot establishes a driving force which allows the single crystal structure to propagate through the solid material 18.
Another method allows the entire process to be carried out with a single furnace setup and increases the speed of the solid state recrystallization. This technique is to leave the ampoule in the furnace as shown in HQ.
1 after the single crystal nucleus is formed and to maintain a temperature gradient in the furnace as shown in FIG. 3 for a period of time. The temperature gradient thus imposed on the solid region 18 adds an additional driving'force to the solid state recrystallization step and increases the rate of single crystal growth.
Since regions 16 and 17 of the ingot were melted in the nucleation step, mass transfer occurred causing the relative concentrations of Hg and Cd to vary through these regions. Therefore even if single crystal structure is formed in regions 16 and 17, they will be of little value. Region 18 remained solid through the process preventing the occurrence of any mass transfer. The single crystal material formed from region 18 will therefore have the same composition as the original ingot.
For a more complete understanding of the present invention and the method by which it is carried out, the following example is provided. This example is intended only to be illustrative and is not intended to delimit the invention in any manner.
The polycrystalline ingot was prepared according to U.S. Pat. No. 3,656,494 as follows. An approximately 20 cm long quartz ampoule having an inside diameter of mm and outside diameter of 16 mm was cleaned in a conventional manner. The ampoule was then loaded with 38.3795 grams of mercury, 5.7165 grams of cadmium, and 30.9040 grams of tellurium. The ampoule was then sealed and reacted overnight at 800C. The ampoule was then oil quenched.
The ingot thus formed was approximately 12 centimeters long and had a uniform composition of Hg Cd Te The ingot was left in the ampoule and placed in a 3 zone furnace with the thermal profile illustrated in FIG. 3. The ampoule was positioned so that approximately 2 centimeters of the ingot was at a temperature above the melting point of this composi tion material. These conditions were maintained for 21 days. The ampoule was then removed from the furnace and cooled and the ingot was removed from the am poule. Upon inspection all the material which remained solid throughout the process was found to be single crystal and homogeneous with the same composition as the originally prepared ingot.
Although the present invention has been shown and illustrated in terms of a specific process, it will be apparent that changes or modifications can be made without departing from the spirit of the invention as defined by the appended claims.
What is claimed is:
1. A method for enhancement of solid state recrystallization of a polycrystalline ternary semiconductor compound consisting of the step of melting a portion of a polycrystalline ternary semiconductor compound ingot and allowing single crystal growth from the liquid to occur at the liquid-solid interface whereby a single crystal mucleus is formed at the liquid-solid interface.
2. A method for enhancement of solid state recrystallization of polycrystalline (Hg,Cd)Te consisting of the step of melting a small .portion of a polycrystalline (Hg,Cd)Te ingot and allowing single crystal growth from the liquid to occur at the liquid-solid interface whereby a single crystal nucleus is formed at the liquidsolid interface.
3. A process for forming single crystal (Hg,Cd)Te material from polycrystalline (Hg,Cd)Te material consisting of the steps of creating a nucleus of single crystal material by melting a small portion of a polycrystalline (Hg,Cd)Te ingot whereby single crystal growth occurs at the liquid solid interface and propagating the crystal structrue through the rest of the ingot by solid state recrystallization.
4. A process according to claim 3 including the step of refreezing the melted portion of said ingot after the nucleus is formed at the liquid solid interface.
5. A process according to claim 3 wherein the polycrystalline'material is of uniform predetermined composition, so that the single crystal material formed by solid state recrystallization is of the same uniform predetermined composition.
6. A process according to claim 3 wherein the solid state recrystallization stepconsists of maintaining the ingot at an elevated temperature below the melting point of the material whereby the single crystal structure propagates from the nucleus through the ingot.
7. A process for forming single crystal (Hg,Cd)Te material from polycrystalline (Hg,Cd)Te consisting of the step of maintaining a temperature gradient throughout an ingot of polycrystalline (Hg,Cd)Te such that a small portion of said material is melted at the high temperature end and the temperature continuously decreases to the low temperature end whereby liquid state single crystal growth occurs at the liquidsolid interface forming a nucleation site from which the single crystal structure is propagated through the solid state portion of the ingot.
8. A process according to claim 7 wherein the polycrystalline material is of uniform predetermined composition, so that the single crystal material formed from the portion which remained solid is of the same uniform composition.
Claims (8)
1. A METHOD FOR ENHANCEMENT OF SOLID STATE RECRYSTALLIZATION OF A POLYCRYSTALLINE TERNARY SEMICONDUCTOR COMPOUND CONSISTING OF THE STEP OF MELTING A PORTION OF A POLYCRYSTALLINE TENARY SEMICONDUCTOR COMPOUND INGOT AND ALLOWING SINGLE CRYSTAL GROWTH FROM THE LIQUID TO OCCUR AT THE LIQUID-SOLID INTERFACE WHEREBY A SINGLE CRYSTAL MUCLEUS IS FORMED AT THE LIQUID-SOLID INTERFACE.
2. A method for enhancement of solid state recrystallization of polycrystalline (Hg,Cd)Te consisting of the step of melting a small portion of a polycrystalline (Hg,Cd)Te ingot and allowing single crystal growth from the liquid to occur at the liquid-solid interface whereby a single crystal nucleus is formed at the liquid-solid interface.
3. A process for forming single crystal (Hg,Cd)Te material from polycrystalline (Hg,Cd)Te material consisting of the steps of creating a nucleus of single crystal material by melting a small portion of a polycrystalline (Hg,Cd)Te ingot whereby sIngle crystal growth occurs at the liquid solid interface and propagating the crystal structrue through the rest of the ingot by solid state recrystallization.
4. A process according to claim 3 including the step of refreezing the melted portion of said ingot after the nucleus is formed at the liquid solid interface.
5. A process according to claim 3 wherein the polycrystalline material is of uniform predetermined composition, so that the single crystal material formed by solid state recrystallization is of the same uniform predetermined composition.
6. A process according to claim 3 wherein the solid state recrystallization step consists of maintaining the ingot at an elevated temperature below the melting point of the material whereby the single crystal structure propagates from the nucleus through the ingot.
7. A process for forming single crystal (Hg,Cd)Te material from polycrystalline (Hg,Cd)Te consisting of the step of maintaining a temperature gradient throughout an ingot of polycrystalline (Hg, Cd)Te such that a small portion of said material is melted at the high temperature end and the temperature continuously decreases to the low temperature end whereby liquid state single crystal growth occurs at the liquid-solid interface forming a nucleation site from which the single crystal structure is propagated through the solid state portion of the ingot.
8. A process according to claim 7 wherein the polycrystalline material is of uniform predetermined composition, so that the single crystal material formed from the portion which remained solid is of the same uniform composition.
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| US00391110A US3849205A (en) | 1973-08-27 | 1973-08-27 | Enhancement of solid state recrystallization by induced nucleation |
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| US00391110A US3849205A (en) | 1973-08-27 | 1973-08-27 | Enhancement of solid state recrystallization by induced nucleation |
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Cited By (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4011074A (en) * | 1974-03-25 | 1977-03-08 | Consortium Fur Elektrochemische Industrie Gmbh | Process for preparing a homogeneous alloy |
| US4249987A (en) * | 1976-04-22 | 1981-02-10 | Hughes Aircraft Company | Method of growing large Pb1-x -Snx -Te single crystals where 0<X<1 |
| EP0053481A1 (en) * | 1980-11-28 | 1982-06-09 | Ngk Insulators, Ltd. | Method for producing a single crystal |
| FR2536767A1 (en) * | 1982-11-30 | 1984-06-01 | Commissariat Energie Atomique | PROCESS FOR PRODUCING TERNAIR OR QUATERNARY SEMICONDUCTOR COMPOUNDS |
| US4465546A (en) * | 1982-09-01 | 1984-08-14 | North American Philips Corporation | Method of growing polycrystalline and monocrystalline bodies of volatile 2,6 and 3,5 compounds in graphite crucibles by self-sealing and self-releasing techniques |
| FR2560225A1 (en) * | 1983-08-17 | 1985-08-30 | Comp Generale Electricite | Improvement to the process of growth in a solvent zone of single crystals exhibiting high vapour pressures and apparatus for its use |
| FR2560226A1 (en) * | 1983-08-17 | 1985-08-30 | Comp Generale Electricite | Process for the preparation of a polycrystalline alloy intended for the production of single crystals by passing through a solvent zone |
| US4578145A (en) * | 1979-07-05 | 1986-03-25 | U.S. Philips Corporation | Method of making monocrystalline ternary semiconductor compounds |
| US4582683A (en) * | 1984-12-03 | 1986-04-15 | Texas Instruments Incorporated | (Hg,Cd,Zn)Te crystal compositions |
| US4588446A (en) * | 1985-02-21 | 1986-05-13 | Texas Instruments Incorporated | Method for producing graded band gap mercury cadmium telluride |
| US4591410A (en) * | 1983-06-24 | 1986-05-27 | Telefunken Electronic Gmbh | Method for the production of monocrystalline Hg1-x Cdx Te |
| EP0214350A1 (en) * | 1985-07-24 | 1987-03-18 | Commissariat A L'energie Atomique | Method for preparing a polycrystalline alloy for making single crystals by a travelling solvent zone |
| US4654196A (en) * | 1983-08-17 | 1987-03-31 | Commissariat A L'energie Atomique | Process for producing a polycrystalline alloy |
| US4690725A (en) * | 1985-11-22 | 1987-09-01 | Cominco Ltd. | Purification of Cd and Te by zone refining |
| US4765863A (en) * | 1986-01-21 | 1988-08-23 | S.A.T. (Societe Anonyme De Telecommunications) | Method of preparing a crystalline ingot of Hg1-x.sbsb.o Cdx.sbsb.o Te |
| US4863553A (en) * | 1982-11-15 | 1989-09-05 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Method of preparing radially homogenous mercury cadmium telluride crystals |
| US5693138A (en) * | 1993-12-22 | 1997-12-02 | Tokin Corporation | Magnetooptical element |
| JP3517094B2 (en) | 1997-07-10 | 2004-04-05 | 矢崎総業株式会社 | Lamp socket |
| US8535440B1 (en) | 2010-04-12 | 2013-09-17 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Method of promoting single crystal growth during melt growth of semiconductors |
| US10184730B2 (en) | 2016-08-17 | 2019-01-22 | Harris Corporation | Phase change cell |
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| US3622399A (en) * | 1968-12-31 | 1971-11-23 | Texas Instruments Inc | Method for preparing single crystal pseudobinary alloys |
| US3656944A (en) * | 1970-02-16 | 1972-04-18 | Texas Instruments Inc | Method of producing homogeneous ingots of a metallic alloy |
| US3723190A (en) * | 1968-10-09 | 1973-03-27 | Honeywell Inc | Process for preparing mercury cadmium telluride |
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| US1793672A (en) * | 1926-02-16 | 1931-02-24 | Percy W Bridgman | Crystals and their manufacture |
| US2953690A (en) * | 1957-09-03 | 1960-09-20 | Nat Res Dev | Photosensitive cells, radiation filters and semiconductor materials for use in such cells and filters |
| US3468363A (en) * | 1967-10-10 | 1969-09-23 | Texas Instruments Inc | Method of producing homogeneous ingots of mercury cadmium telluride |
| US3723190A (en) * | 1968-10-09 | 1973-03-27 | Honeywell Inc | Process for preparing mercury cadmium telluride |
| US3622399A (en) * | 1968-12-31 | 1971-11-23 | Texas Instruments Inc | Method for preparing single crystal pseudobinary alloys |
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Cited By (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4011074A (en) * | 1974-03-25 | 1977-03-08 | Consortium Fur Elektrochemische Industrie Gmbh | Process for preparing a homogeneous alloy |
| US4249987A (en) * | 1976-04-22 | 1981-02-10 | Hughes Aircraft Company | Method of growing large Pb1-x -Snx -Te single crystals where 0<X<1 |
| US4578145A (en) * | 1979-07-05 | 1986-03-25 | U.S. Philips Corporation | Method of making monocrystalline ternary semiconductor compounds |
| EP0053481A1 (en) * | 1980-11-28 | 1982-06-09 | Ngk Insulators, Ltd. | Method for producing a single crystal |
| US4465546A (en) * | 1982-09-01 | 1984-08-14 | North American Philips Corporation | Method of growing polycrystalline and monocrystalline bodies of volatile 2,6 and 3,5 compounds in graphite crucibles by self-sealing and self-releasing techniques |
| US4863553A (en) * | 1982-11-15 | 1989-09-05 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Method of preparing radially homogenous mercury cadmium telluride crystals |
| FR2536767A1 (en) * | 1982-11-30 | 1984-06-01 | Commissariat Energie Atomique | PROCESS FOR PRODUCING TERNAIR OR QUATERNARY SEMICONDUCTOR COMPOUNDS |
| US4564415A (en) * | 1982-11-30 | 1986-01-14 | Commissariat A L'energie Atomique | Process for producing ternary or quaternary semiconductor compounds |
| EP0115715A1 (en) * | 1982-11-30 | 1984-08-15 | Commissariat à l'Energie Atomique | Process for elaborating ternary or quaternary semiconductor compounds |
| US4591410A (en) * | 1983-06-24 | 1986-05-27 | Telefunken Electronic Gmbh | Method for the production of monocrystalline Hg1-x Cdx Te |
| FR2560226A1 (en) * | 1983-08-17 | 1985-08-30 | Comp Generale Electricite | Process for the preparation of a polycrystalline alloy intended for the production of single crystals by passing through a solvent zone |
| FR2560225A1 (en) * | 1983-08-17 | 1985-08-30 | Comp Generale Electricite | Improvement to the process of growth in a solvent zone of single crystals exhibiting high vapour pressures and apparatus for its use |
| US4654196A (en) * | 1983-08-17 | 1987-03-31 | Commissariat A L'energie Atomique | Process for producing a polycrystalline alloy |
| US4582683A (en) * | 1984-12-03 | 1986-04-15 | Texas Instruments Incorporated | (Hg,Cd,Zn)Te crystal compositions |
| US4588446A (en) * | 1985-02-21 | 1986-05-13 | Texas Instruments Incorporated | Method for producing graded band gap mercury cadmium telluride |
| EP0214350A1 (en) * | 1985-07-24 | 1987-03-18 | Commissariat A L'energie Atomique | Method for preparing a polycrystalline alloy for making single crystals by a travelling solvent zone |
| US4690725A (en) * | 1985-11-22 | 1987-09-01 | Cominco Ltd. | Purification of Cd and Te by zone refining |
| US4765863A (en) * | 1986-01-21 | 1988-08-23 | S.A.T. (Societe Anonyme De Telecommunications) | Method of preparing a crystalline ingot of Hg1-x.sbsb.o Cdx.sbsb.o Te |
| US5693138A (en) * | 1993-12-22 | 1997-12-02 | Tokin Corporation | Magnetooptical element |
| JP3517094B2 (en) | 1997-07-10 | 2004-04-05 | 矢崎総業株式会社 | Lamp socket |
| US8535440B1 (en) | 2010-04-12 | 2013-09-17 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Method of promoting single crystal growth during melt growth of semiconductors |
| US10184730B2 (en) | 2016-08-17 | 2019-01-22 | Harris Corporation | Phase change cell |
| US10935328B2 (en) | 2016-08-17 | 2021-03-02 | Harris Corporation | Phase change cell |
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