US3137595A - Method of producing boron-gold alloy foil - Google Patents
Method of producing boron-gold alloy foil Download PDFInfo
- Publication number
- US3137595A US3137595A US21591A US2159160A US3137595A US 3137595 A US3137595 A US 3137595A US 21591 A US21591 A US 21591A US 2159160 A US2159160 A US 2159160A US 3137595 A US3137595 A US 3137595A
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- US
- United States
- Prior art keywords
- boron
- gold
- foil
- powder
- mixture
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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Classifications
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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
- C30B31/00—Diffusion or doping processes for single crystals or homogeneous polycrystalline material with defined structure; Apparatus therefor
- C30B31/02—Diffusion or doping processes for single crystals or homogeneous polycrystalline material with defined structure; Apparatus therefor by contacting with diffusion materials in the solid state
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C5/00—Alloys based on noble metals
- C22C5/02—Alloys based on gold
-
- 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
Definitions
- This invention is based upon our discovery that the boron-containing gold required for such purposes is advantageously produced by first intimately mixing gold powder and boron powder, then compacting the mixture under pressure, thereafter tempering the pressed body at a temperature below the melting temperature of gold, subsequently melting the pressed and sintered body, and thereafter rolling the remelted material down to foil thickness.
- This discovery was made in the face of prior views that boron cannot be melted together with gold because it tends to become expelled from the melt, as explained below.
- solid boron be introduced into the liquid gold-silicon alloy. This can be done, for example, by first mechanically rolling amorphous boron in powder form into a gold foil or by spreading the solid boron in fine distribution upon the foil, whereafter the gold foil is placed upon the semiconductor body and the assembly is subsequently heated. Then the gold forms a liquid alloy with a portion of the semiconductor material, in which alloy the boron penetrates down to the alloying front.
- the boron content of the foil may be 0.001 to 0.3%, being preferably about 0.1%, in respect to the gold, all percentages herein being by Weight.
- a preferred embodiment of the method is as follows.
- Gold powder and boron powder are intimately mixed with each other and are then subjected to pressure.
- the mixture of gold powder and boron powder may contain 0.01 to 0.5% boron.
- An advantageous embodiment of the invention contained 0.35% boron in the powder mixture.
- the finished foil then contains about 0.3% b0- ron, because slight quantities of boron precipitate at the external surfaces. It has been found preferable to apply the highest feasible pressure, for example in the order of 10,000 atm.
- the preferred range of the pressures to be employed is from 10 to 100,000 atmospheres, with a pressure of at least 2000 atmospheres desirable, since higher pressures yield better results.
- the compressed and thus shaped body is tempered in vacuum or protective atmosphere such as nitrogen gas at about 900 C. for several days, preferably at least 48 hours.
- the value of 48 hours as minimum period for the processing time is suitable. Very good results were obtained with periods of 50 to hours.
- the tempering temperature must in any event remain below the melting temperature of gold (1,063 C.).
- the tempering temperature should be at least 825 C. with a temperature of about 900 C. having been found to be particularly favorable.
- the boron content is determined of a portion of the pressed body, and the other portion is melted together with a correspondingly dimensioned quantity of Suitgether with the gold.
- a portion of bismuth may be roasted, i.e., heated with ingress of air, and another portion of bismuth may be sulfurized, i.e., heated in pulverulent form together with sulfur flower to melting.
- corresponding quantities of these two types of prepared bismuth are added to the tempered pressed material, if desired together with another portion of untreated bismuth.
- These melting operations are preferably also performed in vacuum or under protective gas.
- a method of producing boron-containing gold foil for p-doping a body of essentially monocrystalline silicon semiconductor material comprising intimately mixing gold powder and boron powder,'the mixture containing from 0. 01 to 0.5% by'weight of boron powder, compacting the mixture under a pressure between and.
- the boron-containing gold foil having from 0.001 to 0.01% of sulfur in-' corporated therein.
- a method of producing boron-containing gold foil for p-doping a body of essentially monocrystalline silia con semiconductor material comprising intimately mixing gold powder and boron powder, the mixture containing from 0.01 to 0.5 by weight of boron powder, compacting the mixture under pressure, tempering and sintering the compacted mixture at a temperature below the melting point of gold for a period of time suificient to form a boron-goldalloy, subsequently melting the sintered, pressed boron-gold alloy, and thereafter forming the material into a foil, the tempering being carried out for at least a day at atemperature of at least about 900 C., the compacting being at a pressure of at least 2,000 atmospheres. a j V 9.
- a method of producing boron-containing gold foil for p-doping a body" of essentiallymonocrystalline silicon semiconductor material comprising intimately mixing gold powder and boron powder, the mixture containpressure and tempering and sintering the compacted mixture for at least two days at a temperature-of at least 825 C. but below the melting temperature of gold, while under said pressure, subsequently melting the pressed body, and thereafter rolling the re -solidified material down to a foil.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Microelectronics & Electronic Packaging (AREA)
- General Physics & Mathematics (AREA)
- Power Engineering (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Computer Hardware Design (AREA)
- Mechanical Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Physics & Mathematics (AREA)
- Crystallography & Structural Chemistry (AREA)
- Contacts (AREA)
- Powder Metallurgy (AREA)
Description
United States Patent 3,137,595 METHOD OF PRODUCING BORON-GOLD ALLOY FOIL Hubert Patalong, Pretzfeld, Upper Franconia, and Norbert Schink, Erlangen, Germany, assignors to Siemens- Schuckertwerke Aktiengesellschaft, Berlin-Siemeusstadt, Germany, a corporation of Germany No Drawing. Filed Apr. 12, 1960, Ser. No. 21,591 Claims priority, application Germany May 12, 1959 9 Claims. (Cl. 148-1) Our invention relates to a method for producing a p-doped region in bodies consisting of essentially monocrystalline semiconductor material, preferably silicon, by alloying onto the semiconductor body a foil of boroncontaining gold.
This invention is based upon our discovery that the boron-containing gold required for such purposes is advantageously produced by first intimately mixing gold powder and boron powder, then compacting the mixture under pressure, thereafter tempering the pressed body at a temperature below the melting temperature of gold, subsequently melting the pressed and sintered body, and thereafter rolling the remelted material down to foil thickness. This discovery was made in the face of prior views that boron cannot be melted together with gold because it tends to become expelled from the melt, as explained below.
It is known to produce an n-doped region in bodies of silicon by alloying a donor element, for example antimony, into the gold component prior to joining that component with the silicon. It is further known to produce a p-doped region in bodies of semiconductor material by alloying onto the bodies a part consisting of aluminum. This method has the disadvantage of requiring relatively high temperatures (700 C.) whereby the lifetime of the minority charged carriers is more strongly reduced than when alloying gold components into the semiconductor body, the latter method being applicable at a lower alloying temperature (400 to 500 0.).
Many attempts have been made toward making the favorable conditions afforded by the alloying of dopecontaining gold also applicable for the purpose of producing p-doped regions. It has been tried, especially, to thus introduce boron into the semiconductor material, because boron would permit the obtainment of a high doping concentration, due to the high solubility of boron in silicon, the distribution coefiicient being near unity. However, the introduction of boron by diffusion, by a known method, possesses the disadvantage of demanding extremely high temperatures (900 to 1300 C.), thus entailing a great reduction in life-time of the minority carriers. Since boron could not be melted together with gold because it does not dissolve in gold but tends to become expelled from the melt, it has been proposed that solid boron be introduced into the liquid gold-silicon alloy. This can be done, for example, by first mechanically rolling amorphous boron in powder form into a gold foil or by spreading the solid boron in fine distribution upon the foil, whereafter the gold foil is placed upon the semiconductor body and the assembly is subsequently heated. Then the gold forms a liquid alloy with a portion of the semiconductor material, in which alloy the boron penetrates down to the alloying front.
It is an object of our invention to bond a boron-containing gold foil with a semiconductor body by alloying rather than diffusion. More particularly it is an object of the invention to produce boron-containing gold, to prepare foils from such boron-containing gold, and to produce a p-doped region in semiconductor bodies by an alloying method.
We have discovered that by means of the method according to our invention boron becomes dissolvable in gold after all. When gold powder and boron powder are intimately mixed, then kept compacted under pressure and are tempered several days at a temperature below the melting temperature of gold, a suflicient quantity of boron diffuses into the intimately adjacent gold or vice versa, so that in this manner a mixture akin to a borongold alloy results. It has been found that after such processing, the boron is no longer present within the gold in relatively coarse pieces but mainly in molecular distribution. Even during subsequent melting and rolling of the material down to foil thickness, no de-mixing takes place to any appreciable extent.
Consequently, it then becomes feasible to melt the tempered, pressed body together with a further quantity of gold and/or other materials, particularly such other materials that improve the quality of the alloy. For example it has been found preferable to add slight quantities of gallium and/or indium to the gold foil, in amounts of from 0.1 to 1%, preferably 0.3 to 0.4%. These two substances, likewise acting as or known to be acceptors (p-doping), increase the doping concentration here only to a negligible extent, but they greatly facilitate wetting, and the alloy formation, thus affording a considerably improved reliability with respect to the control of the alloying method.
It has further been found favorable to admix in or incorporate with the boron-containing gold foil an additional trace content of oxygen and/ or sulfur, for example, preferably in the order of magnitude of a few millipercent. The quantity of oxygen may be 0.001 to 0.02%, the quantity of sulfur may preferably be 0.001 to 0.01%. This also affords improving the quality of the alloy. Furthermore, slight additional quantities of bismuth, for example 0.01 to 1% and particularly 0.3 to 0.4% relative to the weight of the gold, may be employed. The bismuth addition promotes the occurrence of a planar alloying front. The slight n-doping action cannot produce a detrimental effect due to the strong p-doping action of the boron.
The boron content of the foil may be 0.001 to 0.3%, being preferably about 0.1%, in respect to the gold, all percentages herein being by Weight.
A preferred embodiment of the method is as follows.
Gold powder and boron powder are intimately mixed with each other and are then subjected to pressure. The mixture of gold powder and boron powder may contain 0.01 to 0.5% boron. An advantageous embodiment of the invention contained 0.35% boron in the powder mixture. The finished foil then contains about 0.3% b0- ron, because slight quantities of boron precipitate at the external surfaces. It has been found preferable to apply the highest feasible pressure, for example in the order of 10,000 atm. The preferred range of the pressures to be employed is from 10 to 100,000 atmospheres, with a pressure of at least 2000 atmospheres desirable, since higher pressures yield better results. Thereafter the compressed and thus shaped body is tempered in vacuum or protective atmosphere such as nitrogen gas at about 900 C. for several days, preferably at least 48 hours. The value of 48 hours as minimum period for the processing time is suitable. Very good results were obtained with periods of 50 to hours. The tempering temperature must in any event remain below the melting temperature of gold (1,063 C.). The tempering temperature should be at least 825 C. with a temperature of about 900 C. having been found to be particularly favorable.
Thereafter, the boron content is determined of a portion of the pressed body, and the other portion is melted together with a correspondingly dimensioned quantity of Suitgether with the gold. For example a portion of bismuth may be roasted, i.e., heated with ingress of air, and another portion of bismuth may be sulfurized, i.e., heated in pulverulent form together with sulfur flower to melting. After determining the oxygen and sulfur contents respectively, corresponding quantities of these two types of prepared bismuth are added to the tempered pressed material, if desired together with another portion of untreated bismuth. These melting operations are preferably also performed in vacuum or under protective gas.
We claim:
1. A method of producing boron-containing gold foil for p-doping a body of essentially monocrystalline silicon semiconductor material, comprising intimately mixing gold powder and boron powder,'the mixture containing from 0. 01 to 0.5% by'weight of boron powder, compacting the mixture under a pressure between and.
100,000 atmospheres, tempering and sintering the compacted mixture at a temperature above 825 C. and below the melting point of gold for a period of time sufiicient to form a boron-gold alloy, subsequently melting the sintered, pressed boron-gold alloy, and thereafter forming the material into a foil.
2. The method of claim 1, the tempering being carried out in nitrogen gas.
3. The method of claim 1, the tempering being carried out in vacuum.
4. The method of claim 1, the tempering being carried out for at least a day, the compacting being carried out at at least 2,000 atmospheres pressure.
5. The method defined in claim 1, the boron-containing gold foil having'from 0.001 to 0.02% of oxygen incorporated therein.
. .6. The method defined in claim 1, the boron-containing gold foil having from 0.001 to 0.01% of sulfur in-' corporated therein.
'7. The method defined in claim 1, the boron-containing from 0.01 to 0.5 by Weight of boron powder, compacting the mixture under at least 10,000 atmospheres ing gold foil having 0.01 to therein.
8. A method of producing boron-containing gold foil for p-doping a body of essentially monocrystalline silia con semiconductor material, comprising intimately mixing gold powder and boron powder, the mixture containing from 0.01 to 0.5 by weight of boron powder, compacting the mixture under pressure, tempering and sintering the compacted mixture at a temperature below the melting point of gold for a period of time suificient to form a boron-goldalloy, subsequently melting the sintered, pressed boron-gold alloy, and thereafter forming the material into a foil, the tempering being carried out for at least a day at atemperature of at least about 900 C., the compacting being at a pressure of at least 2,000 atmospheres. a j V 9. A method of producing boron-containing gold foil for p-doping a body" of essentiallymonocrystalline silicon semiconductor material, comprising intimately mixing gold powder and boron powder, the mixture containpressure and tempering and sintering the compacted mixture for at least two days at a temperature-of at least 825 C. but below the melting temperature of gold, while under said pressure, subsequently melting the pressed body, and thereafter rolling the re -solidified material down to a foil.
References Cited in the file of this patent- Treatiseon Powder Metallurgy, Goetzel, Interscience Publishers, Inc., New York, 1950. Relied on page487.
1% of bismuth incorporated
Claims (1)
1. A METHOD OF PRODUCING BORON-CONTAINING GOLD FOIL FOR P-DOPING A BODY OF ESSENTIALLY MONOCRYSTALLINE SILICON SEMICONDUCTOR MATERIAL, COMPRISING INTIMATELY MIXING GOLD POWDER AND BORON POWDER, THE MIXTURE CONTAINING FROM 0.01 TO 0.5% BY WEIGHT OF BORON POWDER, COMPACTING THE MIXTURE UNDER A PRESSURE BETWEEN 10 AND 100,000 ATMOSPHERES, TEMPERING AND SINTERING THE COMPACTED MIXTURE AT A TEMPERATURE ABOVE 825*C. AND BELOW THE MELTING POINT OF GOLD FOR A PERIOD OF TIME SUFFICIENT TO FORM A BORON-GOLD ALLOY, SUBSEQUENTLY MELTING THE SINTERED, PRESSED BORON-GOLD ALLOY, AND THEREAFTER FORMING THE MATERIAL INTO A FOIL.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DES0062963 | 1959-05-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3137595A true US3137595A (en) | 1964-06-16 |
Family
ID=7496010
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US21591A Expired - Lifetime US3137595A (en) | 1959-05-12 | 1960-04-12 | Method of producing boron-gold alloy foil |
Country Status (5)
Country | Link |
---|---|
US (1) | US3137595A (en) |
BE (2) | BE590792A (en) |
CH (1) | CH398797A (en) |
FR (1) | FR1244844A (en) |
GB (1) | GB911235A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3211550A (en) * | 1959-11-02 | 1965-10-12 | Hughes Aircraft Co | Gold boron alloy and method of making the same |
US3214653A (en) * | 1959-11-02 | 1965-10-26 | Hughes Aircraft Co | Gold bonded, boron containing semiconductor devices |
US3339269A (en) * | 1962-03-15 | 1967-09-05 | Gen Motors Corp | Method of bonding |
US4005454A (en) * | 1975-04-05 | 1977-01-25 | Semikron Gesellschaft Fur Gleichrichterbau Und Elektronik M.B.H. | Semiconductor device having a solderable contacting coating on its opposite surfaces |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2686118A (en) * | 1952-12-23 | 1954-08-10 | Ontario Research Foundation | Method of making metal products directly from ores |
US2701326A (en) * | 1949-11-30 | 1955-02-01 | Bell Telephone Labor Inc | Semiconductor translating device |
US2937113A (en) * | 1956-05-15 | 1960-05-17 | Siemens Ag | Method of producing an electrodecarrying silicon semiconductor device |
US2965519A (en) * | 1958-11-06 | 1960-12-20 | Bell Telephone Labor Inc | Method of making improved contacts to semiconductors |
US3009840A (en) * | 1958-02-04 | 1961-11-21 | Siemens Ag | Method of producing a semiconductor device of the junction type |
US3068127A (en) * | 1959-06-02 | 1962-12-11 | Siemens Ag | Method of producing a highly doped p-type zone and an appertaining contact on a semiconductor crystal |
-
0
- BE BE590762D patent/BE590762A/xx unknown
- BE BE590792D patent/BE590792A/xx unknown
-
1960
- 1960-01-11 FR FR815343A patent/FR1244844A/en not_active Expired
- 1960-01-18 GB GB1783/60A patent/GB911235A/en not_active Expired
- 1960-04-12 US US21591A patent/US3137595A/en not_active Expired - Lifetime
- 1960-04-20 CH CH440660A patent/CH398797A/en unknown
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2701326A (en) * | 1949-11-30 | 1955-02-01 | Bell Telephone Labor Inc | Semiconductor translating device |
US2686118A (en) * | 1952-12-23 | 1954-08-10 | Ontario Research Foundation | Method of making metal products directly from ores |
US2937113A (en) * | 1956-05-15 | 1960-05-17 | Siemens Ag | Method of producing an electrodecarrying silicon semiconductor device |
US2974074A (en) * | 1956-05-15 | 1961-03-07 | Siemens Ag | Method of producing a silicon semiconductor device |
US3009840A (en) * | 1958-02-04 | 1961-11-21 | Siemens Ag | Method of producing a semiconductor device of the junction type |
US2965519A (en) * | 1958-11-06 | 1960-12-20 | Bell Telephone Labor Inc | Method of making improved contacts to semiconductors |
US3068127A (en) * | 1959-06-02 | 1962-12-11 | Siemens Ag | Method of producing a highly doped p-type zone and an appertaining contact on a semiconductor crystal |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3211550A (en) * | 1959-11-02 | 1965-10-12 | Hughes Aircraft Co | Gold boron alloy and method of making the same |
US3214653A (en) * | 1959-11-02 | 1965-10-26 | Hughes Aircraft Co | Gold bonded, boron containing semiconductor devices |
US3339269A (en) * | 1962-03-15 | 1967-09-05 | Gen Motors Corp | Method of bonding |
US4005454A (en) * | 1975-04-05 | 1977-01-25 | Semikron Gesellschaft Fur Gleichrichterbau Und Elektronik M.B.H. | Semiconductor device having a solderable contacting coating on its opposite surfaces |
Also Published As
Publication number | Publication date |
---|---|
BE590792A (en) | |
FR1244844A (en) | 1960-10-28 |
CH398797A (en) | 1966-03-15 |
BE590762A (en) | |
GB911235A (en) | 1962-11-21 |
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