US2808315A - Processing of silicon - Google Patents
Processing of silicon Download PDFInfo
- Publication number
- US2808315A US2808315A US559258A US55925856A US2808315A US 2808315 A US2808315 A US 2808315A US 559258 A US559258 A US 559258A US 55925856 A US55925856 A US 55925856A US 2808315 A US2808315 A US 2808315A
- Authority
- US
- United States
- Prior art keywords
- lifetime
- silicon
- cooling
- per minute
- temperature
- 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
Links
- 229910052710 silicon Inorganic materials 0.000 title description 20
- 239000010703 silicon Substances 0.000 title description 20
- 238000012545 processing Methods 0.000 title description 3
- 238000001816 cooling Methods 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 22
- 229910021421 monocrystalline silicon Inorganic materials 0.000 claims description 13
- 230000015556 catabolic process Effects 0.000 claims description 6
- 238000006731 degradation reaction Methods 0.000 claims description 6
- 230000000670 limiting effect Effects 0.000 claims description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 19
- 238000010438 heat treatment Methods 0.000 description 17
- 238000010791 quenching Methods 0.000 description 16
- 238000000137 annealing Methods 0.000 description 15
- 239000000463 material Substances 0.000 description 14
- 239000013078 crystal Substances 0.000 description 13
- 230000000171 quenching effect Effects 0.000 description 11
- 238000011084 recovery Methods 0.000 description 10
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000003921 oil Substances 0.000 description 4
- 238000010583 slow cooling Methods 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 230000009286 beneficial effect Effects 0.000 description 3
- 230000001965 increasing effect Effects 0.000 description 3
- 230000006798 recombination Effects 0.000 description 3
- 238000005215 recombination Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 230000002411 adverse Effects 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 238000013459 approach Methods 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
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000002800 charge carrier Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B33/00—Silicon; Compounds thereof
- C01B33/02—Silicon
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F3/00—Changing the physical structure of non-ferrous metals or alloys by special physical methods, e.g. treatment with neutrons
-
- 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
-
- 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
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/22—Diffusion of impurity materials, e.g. doping materials, electrode materials, into or out of a semiconductor body, or between semiconductor regions; Interactions between two or more impurities; Redistribution of impurities
-
- 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
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/324—Thermal treatment for modifying the properties of semiconductor bodies, e.g. annealing, sintering
-
- 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
- Y10S438/904—Charge carrier lifetime control
Definitions
- Curves A and B represent specimens which were cooled from various temperatures by withdrawing the specimens from a furnace at the indicated temperature and, in the case of curve A, quenching by immersion in an oil such as castor oil, octoil, and ethylene glycol, at room temperature, 20 C., within about a second of their withdrawal from the furnace, or, in the case of curve B, by quenching in air. Oil quenching cools the specimen at a rate of about 1000 C. in 0.1 second while air quenching offers a rate of about 1000" C. per minute.
- an oil such as castor oil, octoil, and ethylene glycol
- T-hese heat treatments have improved the lifetime of material of a wide range of resistivities extending from less than two to more than 300 ohm-centimeters.
- Curves C, D, and E represent the cooling of specimens heated over a range of temperatures including substantially higher temperatures at rates of 20 C. per minute, 3 C. per minute, and 0.5 C. per minute, respectively. It is apparent from these curves that as the cooling rate is decreased the lifetime for a particular material is enhanced substantially. Thus, at 750 C. that material which has a lifetime of less than one microsecond for air quenching has about 15 microseconds at a cooling rate of 20 C. per minute, about 50 microseconds at a cooling rate of 3 C. per minute, and about 61 microseconds for a cooling rate of 05 C. per minute.
- Fig. l The results shown in Fig. l are attributable to the cooling cycles and apparently are independent of such parameters as heat treating ambient, surface treatment, and specimen size. In particular, similar results have been :obtained in vacuum ambients or while'heat treating in helium, hydrogen, and nitrogen. Further, bulk lifetime characteristics arenot altered by the creation of an oxidizing film during the heat treating processf The above results are typical of those for single crystal silicon.
- the process of lifetime improvement is reversible so that the degradation of lifetime incidental to the rapid cooling of silicon can be at least partially overcome by an appropriate heat treatment.
- the maximum cooling rate for effective lifetime maintenance or recovery appears to be about 20 C. per minute down to 400 C. from any temperature below about 1200 C. In all instances higher lifetimes are realized with lower cooling rates.
- Another successful technique for enhancing minority carrier lifetime in single crystal silicon involves maintaining the silicon at elevated temperatures for an interval sufficient for the equilibrium distribution of recombination centers for that temperature to be reached.
- a silicon body which has been cooled by the usual technique of withdrawal from a heat treating furnace, from maximum to room temperature in a few minutes so that its lifetime is low, can have its lifetime enhanced by re heating for a reasonable interval.
- Figs. 2, 3, and 4 illustrate the effects of heat treatments on single crystal silicon bars containing grown n-p junctions. These bars had been subjected to a heating cycle including an oil quench from the maximum temperature of the cycle. Silicon which had an initial lifetime of about 40 microseconds was degraded to about nine microseconds by a quench from 450 C., to about two microseconds by a quench from 580 C., and to less than 0.2 microsecond by a quench from 710 C.
- the length of time required to complete the redistribution of recombination centers in silicon for a particular quenching cycle decreases as the annealing temperature approaches the temperature from which the specimen was quenched.
- the degradation of lifetime is less for low temperature quenches and lifetime recovery is accomplished in a shorter anneal time and is more complete.
- At an anneal of 425 C.'for about two minutes essentially all of the lifetime lost in a quench from 450 C. is recovered.
- About 0.9 of the initial lifetime is recovered with a 425 C. anneal for about two minutes for silicon quenched at 580 C. However, no recovery is noted even at a 450 C. anneal for a sample quenched from 710 C.
- Annealing has been established to afford essentially complete recovery of lost lifetime in silicon in material quenched from temperatures below about 600 C. when the anneal is for the order of a few minutes, about ten minutes, and is at a temperature approaching that from which quenching occurred. Above about 600 C. lifetime recovery for quenched material is incomplete and the lifetime recovery is imperceptible for samples quenched from temperatures above about 900 C. As shown in Fig. 4, only 0.4 of the original lifetime could be recovered by annealing even at 700 C. The degree of recovery possible by annealing of quenched samples is inversely related to the temperature from which quenching occurred in the range of about 600 C. to about 900 C.
- Thesilicon can be cooled to.roomrtemperature and reheated or it can be cooled to the annealing temperajunction which were markedly degraded by heat treatments which were much less severe from the standpoint of lifetime than those typical of the type heretofore employed in diffusing substances into silicon.
- the samples were cooled from the heat treatment temperatures at a rate of 20 C. per minute and after their lifetimes were again measured, they were reheated for an annealing cycle from which they were cooled at 20 C. per minute.
- a bar having a 30 ohm-centimeters n-type region contiguous with an 0.03 ohm-centimeters p-type region exhibited an original lifetime of 28 microseconds which was degraded to two microseconds by a heat treatment at 950 C. for ten minutes and recovered to nine microseconds when annealed at 730 C. for four hours.
- Another sample having an n-type resistivity of 23 ohm-centimeters adjacent a p-type zone of 0.11 ohm-centimeters had its original lifetime of 20 microseconds degraded to less than 0.5 microsecond by a 1100 C. heat treatment for one-half hour. This sample exhibited a lifetime of four microseconds when heat treated at 750 C.
- Another technique and that which is most beneficial from the standpoint of lifetime in single crystal silicon heated to temperatures in excess of 700 C. is to cool the silicon at 05 C. per minute from the maximum to about 700 C. From 700 C. the silicon can be cooled at 20 C. per minute to below about 400 C. Specimens cooled in this manner from a temperature of 1250 C have exhibited lifetimes of four microseconds.
- These treatments may be a cooling of the specimen at less than C. per minute and advantageously at about 05 C. per minute, from the maximum heat treating temperature to about 400 C., by annealing the specimen between 400 C. and800' C. followed by slow cooling to below about 400 C., or by a combination of these techniques.
- the method of limiting the thermal degradation of minority carrier lifetime comprising cooling said body from said elevated temperature to below 400 C. at a maximum rate of 20 C. per minute.
- the method of limiting the thermal degradation of minority carrier lifetime comprising the steps of cooling at a maximum rate of 0.5" C. per minute from the elevated temperature to below 400 C.
- the method of limiting the thermal degradation of minority carrier lifetime comprising the steps of cooling at a maximum rate of 0.5 C. per minute from the elevated temperature to a temperature about 700 C., and cooling at a maximum rate of 20 C. per minute to below 400 C.
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Computer Hardware Design (AREA)
- Organic Chemistry (AREA)
- Power Engineering (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Manufacturing & Machinery (AREA)
- General Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Inorganic Chemistry (AREA)
- Metallurgy (AREA)
- Crystallography & Structural Chemistry (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
Description
Oct. 1, 1957 e. BEMSKI PROCESSING OF smcou 2' Sheets-Sheet 2 Filed Jan. 16, 1956 FIG. 3 OUENCHED FROM 580 c IOOO IO TIME IN (MINUTES) a 5 z o Qmqvnwkki EORUTQK V 0. o "m 0 P c m a O n o W w M 5 4m 76. 5 nm 1 H Fm H C N w o 2 0 M M M o TIME IN (MINUTES)- lNl/ENTOR G. BEMS/(l BJ ATTORNEY water. Curves A and B represent specimens which were cooled from various temperatures by withdrawing the specimens from a furnace at the indicated temperature and, in the case of curve A, quenching by immersion in an oil such as castor oil, octoil, and ethylene glycol, at room temperature, 20 C., within about a second of their withdrawal from the furnace, or, in the case of curve B, by quenching in air. Oil quenching cools the specimen at a rate of about 1000 C. in 0.1 second while air quenching offers a rate of about 1000" C. per minute.
While the specific results reported are for lifetimes of the high resistivity material adjacent a grown n-p junction, it is to be understood that the techniques and results set forth herein are typical of single crystal silicon of both conductivity types. Further, a behavior after the heat treatments of this invention which is similar to that observed for p-n junctions, has been demonstrated in monocrystalline silicon bodies of a single conductivity type by photoconductivity decay type of measurements.
' T-hese heat treatments have improved the lifetime of material of a wide range of resistivities extending from less than two to more than 300 ohm-centimeters.
Heretofore, difiusion and alloying techniques have usually involved a cooling such as depicted in curve B, namely the withdrawal of the specimen from the furnace with a rather rapid cooling rate. The p-type material from which these results were obtained initially exhibited a bulk lifetime of about 50 microseconds. It will be noted that oil quenching from 650 C. reduces this lifetime to less than one microsecond as does air quenching from 750 C.
Curves C, D, and E, on the other hand, represent the cooling of specimens heated over a range of temperatures including substantially higher temperatures at rates of 20 C. per minute, 3 C. per minute, and 0.5 C. per minute, respectively. It is apparent from these curves that as the cooling rate is decreased the lifetime for a particular material is enhanced substantially. Thus, at 750 C. that material which has a lifetime of less than one microsecond for air quenching has about 15 microseconds at a cooling rate of 20 C. per minute, about 50 microseconds at a cooling rate of 3 C. per minute, and about 61 microseconds for a cooling rate of 05 C. per minute. In addition, it will be noted that a five microseconds lifetime can be maintained for material subjected to temperatures in excess of 1050 C. if cooled at a rate of 05 C. per minute while air cooled material can only be maintained at that lifetime when heated to a maximum of 600 C.
The results shown in Fig. l are attributable to the cooling cycles and apparently are independent of such parameters as heat treating ambient, surface treatment, and specimen size. In particular, similar results have been :obtained in vacuum ambients or while'heat treating in helium, hydrogen, and nitrogen. Further, bulk lifetime characteristics arenot altered by the creation of an oxidizing film during the heat treating processf The above results are typical of those for single crystal silicon. The process of lifetime improvement is reversible so that the degradation of lifetime incidental to the rapid cooling of silicon can be at least partially overcome by an appropriate heat treatment. The maximum cooling rate for effective lifetime maintenance or recovery appears to be about 20 C. per minute down to 400 C. from any temperature below about 1200 C. In all instances higher lifetimes are realized with lower cooling rates. Slow cooling appears to offer no beneficial effects with regard to lifetime below about 400 C. These cooling rates also can be effective to enhance the lifetime in the original crystal by employing suitablemeans to retard the cooling of the solidified material following crystal growth from the time it reaches 1200 C. to the time it cools to 400 C. Thus, not only is a process of this natureetfective upon single crystal silicon which has had its lifetime degraded by a high temperature treatment, followed by a rapid cooling, but also to enhance the lifetime of silicon as it is grown over that obtainable heretofore.
The underlying reason for the amove-mentioned phenomenon has not been definitely established. Such evidence as is available, however, indicates that the thermal treatment of silicon determines the distribution of recombination centers therein. The changes in lifetime are at present believed to be due to interactions between crystal imperfections.
Another successful technique for enhancing minority carrier lifetime in single crystal silicon involves maintaining the silicon at elevated temperatures for an interval sufficient for the equilibrium distribution of recombination centers for that temperature to be reached. Thus, a silicon body which has been cooled by the usual technique of withdrawal from a heat treating furnace, from maximum to room temperature in a few minutes so that its lifetime is low, can have its lifetime enhanced by re heating for a reasonable interval.
The curves of Figs. 2, 3, and 4 illustrate the effects of heat treatments on single crystal silicon bars containing grown n-p junctions. These bars had been subjected to a heating cycle including an oil quench from the maximum temperature of the cycle. Silicon which had an initial lifetime of about 40 microseconds was degraded to about nine microseconds by a quench from 450 C., to about two microseconds by a quench from 580 C., and to less than 0.2 microsecond by a quench from 710 C.
' Some recovery of lifetime has been noted for even very low temperature anneals, particularly for the quenches from low temperature. However, the maximum recovery is realized by reheating for at least several minutes to a temperature near that from which the silicon was quenched. Since the lifetime of the material is not adversely affected by the rate of cooling below about 400 C., provided that rate does not exceed that of the usual room air cooling, a slow cooling rate is effective in improving lifetime primarily in the range from the maximum annealing temperature down to 400 C.
As illustrated in Figs. 2, 3, and 4, the length of time required to complete the redistribution of recombination centers in silicon for a particular quenching cycle decreases as the annealing temperature approaches the temperature from which the specimen was quenched. The degradation of lifetime is less for low temperature quenches and lifetime recovery is accomplished in a shorter anneal time and is more complete. At an anneal of 425 C.'for about two minutes essentially all of the lifetime lost in a quench from 450 C. is recovered. About 0.9 of the initial lifetime is recovered with a 425 C. anneal for about two minutes for silicon quenched at 580 C. However, no recovery is noted even at a 450 C. anneal for a sample quenched from 710 C.
Annealing has been established to afford essentially complete recovery of lost lifetime in silicon in material quenched from temperatures below about 600 C. when the anneal is for the order of a few minutes, about ten minutes, and is at a temperature approaching that from which quenching occurred. Above about 600 C. lifetime recovery for quenched material is incomplete and the lifetime recovery is imperceptible for samples quenched from temperatures above about 900 C. As shown in Fig. 4, only 0.4 of the original lifetime could be recovered by annealing even at 700 C. The degree of recovery possible by annealing of quenched samples is inversely related to the temperature from which quenching occurred in the range of about 600 C. to about 900 C.
Results similar to those depicted in Fig. l for the very low cooling rates have been achieved by employing the heat treating or annealing process discussed above. Samples heated to temperatures of from 1000 C. to 1200 C. for varying lengths of time have exhibited bulk lifetimes of the same magnitude as shown for cooling rates --of-;5 C. -per minute-and'less'=when-' wbied=-at-anate of "20- 0. per minute *flom-these"ternperattu'es followd by an anneal in-the- 700' C."to"900 C. range for intervals of from 30 minutes to four hours. Some improvement is obtained even outsidethis range"offfannealing temperatures, specifically, in the'irangefrom 400" C. to 900 \C. Thesilicon can be cooled to.roomrtemperature and reheated or it can be cooled to the annealing temperajunction which were markedly degraded by heat treatments which were much less severe from the standpoint of lifetime than those typical of the type heretofore employed in diffusing substances into silicon. The samples were cooled from the heat treatment temperatures at a rate of 20 C. per minute and after their lifetimes were again measured, they were reheated for an annealing cycle from which they were cooled at 20 C. per minute. A bar having a 30 ohm-centimeters n-type region contiguous with an 0.03 ohm-centimeters p-type region exhibited an original lifetime of 28 microseconds which was degraded to two microseconds by a heat treatment at 950 C. for ten minutes and recovered to nine microseconds when annealed at 730 C. for four hours. Another sample having an n-type resistivity of 23 ohm-centimeters adjacent a p-type zone of 0.11 ohm-centimeters had its original lifetime of 20 microseconds degraded to less than 0.5 microsecond by a 1100 C. heat treatment for one-half hour. This sample exhibited a lifetime of four microseconds when heat treated at 750 C. for four hours. Similar results were observed for the electron lifetime in p-type material in a sample having an 0.1 ohm-centimeter n-type zone adjacent a' 65 ohm-centimeters p-type zone wherein the lifetime initially was six microseconds and was degraded to less than 0.5 microsecond by a 1150 C. heat treatment for one-half hour. A heat treatment at 760 C. for four hours produced a final lifetime of three microseconds.
Another technique and that which is most beneficial from the standpoint of lifetime in single crystal silicon heated to temperatures in excess of 700 C. is to cool the silicon at 05 C. per minute from the maximum to about 700 C. From 700 C. the silicon can be cooled at 20 C. per minute to below about 400 C. Specimens cooled in this manner from a temperature of 1250 C have exhibited lifetimes of four microseconds.
Most of the specific examples discussed above have involved the reduction in the loss of lifetime or the regaining of a portion of the lost lifetime of silicon single crystals subject to rapid cooling. The slow cooling principles have been found to be beneficial even to the extent of increasing the lifetime of material as derived from a pulled single crystal. Thus, portions of single crystals of silicon containing p-n junctions formed from material undoped on the originally grown p side and arsenic doped while rotated three-quarters revolution per minute in accordance with the application of N. B. Hannay, Serial No. 432,792 filed May 27, 1954, and entitled Method of Forming Junctions in Silicon, have been increased in lifetime by appropriate heat treatments, one such crystal exhibiting a resistivity on the p side of 25 ohm-centimeters and on the n side of two ohm-centimeters and an electron lifetime on the p side of 25 microseconds, had its lifetime increased on the p side to 50 microseconds by a ten minute anneal at 500 C. when cooled at a rate of 20 C. per minute to below 400 C. Similar improvements have been realized with grown junctions of other Summarizing the above results, it has been determined that the lifetime in single crystal silicon bodies can be enhanced or its loss as a result of heat treatments above' about 400 C. reduced by appropriate heat treatments. These treatments may be a cooling of the specimen at less than C. per minute and advantageously at about 05 C. per minute, from the maximum heat treating temperature to about 400 C., by annealing the specimen between 400 C. and800' C. followed by slow cooling to below about 400 C., or by a combination of these techniques.
The processes set forth above are merely exemplary and are not to be interpreted as placing the limits thereof upon this invention. Other processing parameters than those set forth in the examples may be employed in practicing this invention without departing from its spirit and scope.
It is to be noted that another method of fabricating silicon bodies having long bulk lifetimes for use in semiconductive translators is disclosed in my application Serial No. 559,259 filed herewith.
What is claimed is:
1. In the process of manufacturing a single crystal silicon body wherein said body is subjected to an elevated temperature in excess of 400 C. the method of limiting the thermal degradation of minority carrier lifetime comprising cooling said body from said elevated temperature to below 400 C. at a maximum rate of 20 C. per minute.
2. In the process of manufacturing a single crystal silicon body wherein said body is subjected to an elevated temperature above 1150 C. the method of limiting the thermal degradation of minority carrier lifetime comprising the steps of cooling at a maximum rate of 0.5" C. per minute from the elevated temperature to below 400 C.
3. In the process of manufacturing a single crystal silicon body wherein said body is subjected to an elevated temperature in the range of 1000 C. to 1200 C., comprising the steps of cooling at a maximum rate of 20 C. per minute to an annealing temperature in the range of 700 C. to 900 C., maintaining said body at said annealing temperature for a period of from minutes to four hours, and cooling to below 400 C. at a maximum rate of 20 C. per minute.
4. In the process of manufacturing a single crystal silicon body wherein said body is subjected to an elevated temperature in excess of 700 C., the method of limiting the thermal degradation of minority carrier lifetime comprising the steps of cooling at a maximum rate of 0.5 C. per minute from the elevated temperature to a temperature about 700 C., and cooling at a maximum rate of 20 C. per minute to below 400 C.
5. The method of essentially complete recovery of minority charge carrier lifetime which has been lost as a result of quenching a single crystal body of silicon from a temperature in the range of 400 C. to 600 C. which comprises the steps of heating the single crystal to an'annealing temperature near that from which said crystal was quenched, maintaining said body at said annealing temperature for a period of several minutes, and
7 8 cooling at a maximum rate of 20 C; per minute'to below maintaining said body at said annealing temperature for 400 C. a period of several minutes, and cooling at a maximum 6. The method of partially regaining minority charge 'rate of 20 C. Pei-minute to below 400 C. carrier lifetime which has been lost as a result of quench- V a w 7 ing a single crystal body of silicon from a temperature 5 References Cited 11 he fi Of this Patent in the range of 400 C. to 900 C. which comprises the UNITED STATES PATENTS steps of heating the single crystal to an annealing temperature near that from which said crystal was quenched, 27432o0 Hannay 1956
Claims (1)
1. IN THE PROCESS OF MANUFACTURINGA SINGLE CRYSTAL SILICON BODY WHEREIN SAID BODY IS SUBJECTED TO AN ELEVATED TEMPERATURE IN EXCESS OF 400*C. THE METHOD OF LIMITING THE THERMAL DEGRADATION OF MINORITY CARRIER LIFETIME COMPRISING COOLING SAID BODY FROM SAID ELEVATED TEMPERATURE TO BELOW 400*C. AT A MAXIMUM RATE 20* C. PER MINUTE.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US559258A US2808315A (en) | 1956-01-16 | 1956-01-16 | Processing of silicon |
FR1170789D FR1170789A (en) | 1956-01-16 | 1957-01-05 | Method for increasing the average lifetime of minority electrified carriers in silicon single crystals |
GB722/57A GB832248A (en) | 1956-01-16 | 1957-01-08 | Improvements in or relating to methods of treating single crystal silicon bodies |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US559258A US2808315A (en) | 1956-01-16 | 1956-01-16 | Processing of silicon |
Publications (1)
Publication Number | Publication Date |
---|---|
US2808315A true US2808315A (en) | 1957-10-01 |
Family
ID=24232926
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US559258A Expired - Lifetime US2808315A (en) | 1956-01-16 | 1956-01-16 | Processing of silicon |
Country Status (3)
Country | Link |
---|---|
US (1) | US2808315A (en) |
FR (1) | FR1170789A (en) |
GB (1) | GB832248A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2953438A (en) * | 1958-01-30 | 1960-09-20 | Gen Electric Co Ltd | Heat treatment of silicon |
DE1106879B (en) * | 1959-03-11 | 1961-05-18 | Siemens Ag | Process for reducing recombination on the surfaces of p-zones of semiconductor devices |
US2992080A (en) * | 1958-07-25 | 1961-07-11 | Gen Electric | Method of improving the purity of silicon |
US3047437A (en) * | 1957-08-19 | 1962-07-31 | Int Rectifier Corp | Method of making a rectifier |
DE1283814B (en) * | 1965-01-20 | 1968-11-28 | Siemens Ag | Process for stabilizing the electrical conductivity of silicon |
DE1286644B (en) * | 1959-10-28 | 1969-01-09 | Western Electric Co | Method for diffusing out doping impurities from a semiconductor body |
US20130192516A1 (en) * | 2012-01-27 | 2013-08-01 | Memc Singapore Pte. Ltd. (Uen200614794D) | Method of preparing cast silicon by directional solidification |
CN117810078A (en) * | 2024-03-01 | 2024-04-02 | 合肥晶合集成电路股份有限公司 | Annealing method |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2743200A (en) * | 1954-05-27 | 1956-04-24 | Bell Telephone Labor Inc | Method of forming junctions in silicon |
-
1956
- 1956-01-16 US US559258A patent/US2808315A/en not_active Expired - Lifetime
-
1957
- 1957-01-05 FR FR1170789D patent/FR1170789A/en not_active Expired
- 1957-01-08 GB GB722/57A patent/GB832248A/en not_active Expired
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2743200A (en) * | 1954-05-27 | 1956-04-24 | Bell Telephone Labor Inc | Method of forming junctions in silicon |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3047437A (en) * | 1957-08-19 | 1962-07-31 | Int Rectifier Corp | Method of making a rectifier |
US2953438A (en) * | 1958-01-30 | 1960-09-20 | Gen Electric Co Ltd | Heat treatment of silicon |
US2992080A (en) * | 1958-07-25 | 1961-07-11 | Gen Electric | Method of improving the purity of silicon |
DE1106879B (en) * | 1959-03-11 | 1961-05-18 | Siemens Ag | Process for reducing recombination on the surfaces of p-zones of semiconductor devices |
DE1286644B (en) * | 1959-10-28 | 1969-01-09 | Western Electric Co | Method for diffusing out doping impurities from a semiconductor body |
DE1283814B (en) * | 1965-01-20 | 1968-11-28 | Siemens Ag | Process for stabilizing the electrical conductivity of silicon |
US20130192516A1 (en) * | 2012-01-27 | 2013-08-01 | Memc Singapore Pte. Ltd. (Uen200614794D) | Method of preparing cast silicon by directional solidification |
CN117810078A (en) * | 2024-03-01 | 2024-04-02 | 合肥晶合集成电路股份有限公司 | Annealing method |
CN117810078B (en) * | 2024-03-01 | 2024-05-28 | 合肥晶合集成电路股份有限公司 | Annealing method |
Also Published As
Publication number | Publication date |
---|---|
FR1170789A (en) | 1959-01-19 |
GB832248A (en) | 1960-04-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4314595A (en) | Method of forming nondefective zone in silicon single crystal wafer by two stage-heat treatment | |
US2957789A (en) | Semiconductor devices and methods of preparing the same | |
JPS603130A (en) | Method of forming no defect surface layer of silicon wafer | |
Yamamoto et al. | Lifetime improvement in Czochralski‐grown silicon wafers by the use of a two‐step annealing | |
US2808315A (en) | Processing of silicon | |
US2827436A (en) | Method of improving the minority carrier lifetime in a single crystal silicon body | |
Schibli et al. | Deep impurities in silicon | |
JPH0787187B2 (en) | Method for manufacturing GaAs compound semiconductor substrate | |
US2806807A (en) | Method of making contacts to semiconductor bodies | |
Shimura | Intrinsic/Internal Gettering in Czochralski Silicon Wafers | |
US4046608A (en) | Method of producing semiconductor components and product thereof | |
JPH0513119B2 (en) | ||
Ono et al. | Oxygen Precipitation Behavior in 300 mm Polished Czorchralski Silicon Wafers | |
US2785096A (en) | Manufacture of junction-containing silicon crystals | |
Swaminathan et al. | Photoluminescence from annealed semi‐insulating GaAs crystals: The 1.360‐eV band | |
JPH033244A (en) | Heat treatment method for semiconductor silicon substrate | |
US3821038A (en) | Method for fabricating semiconductor structures with minimum crystallographic defects | |
Martinuzzi et al. | Influence of oxygen on external phosphorus gettering in disordered silicon wafers | |
US3663321A (en) | Alloy diode characteristics control method | |
JPH02260521A (en) | Article having polycrystalline si semiconductor thin film and manufacture thereof | |
US4264914A (en) | Wide-band-gap, alkaline-earth-oxide semiconductor and devices utilizing same | |
JPS6326541B2 (en) | ||
US3453154A (en) | Process for establishing low zener breakdown voltages in semiconductor regulators | |
Gorelkinskii et al. | Metastable defect states in hydrogen-implanted silicon | |
JPS583236A (en) | Manufacture of gallium arsenide element |