GB2190400A - Process for growing GaAs monocrystal film - Google Patents
Process for growing GaAs monocrystal film Download PDFInfo
- Publication number
- GB2190400A GB2190400A GB08612024A GB8612024A GB2190400A GB 2190400 A GB2190400 A GB 2190400A GB 08612024 A GB08612024 A GB 08612024A GB 8612024 A GB8612024 A GB 8612024A GB 2190400 A GB2190400 A GB 2190400A
- Authority
- GB
- United Kingdom
- Prior art keywords
- growing
- teg
- gas
- gaas
- base
- 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.)
- Granted
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B25/00—Single-crystal growth by chemical reaction of reactive gases, e.g. chemical vapour-deposition growth
- C30B25/02—Epitaxial-layer growth
-
- 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
- C30B29/40—AIIIBV compounds wherein A is B, Al, Ga, In or Tl and B is N, P, As, Sb or Bi
- C30B29/42—Gallium arsenide
-
- 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
- C30B29/60—Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape characterised by shape
- C30B29/68—Crystals with laminate structure, e.g. "superlattices"
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Crystallography & Structural Chemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
Abstract
Triethylgallium (TEG) and arsine (AsH3) are used as gaseous compounds for growing a GaAs monocrystal semiconductor film. One gas is introduced into the vacuum tank and then discharged after the passage of a predetermined time, and the other gas is introduced thereinto and the discharged after the passage of a predetermined time whereby a crystal for one molecular layer grows. By use of TEG as a gallium source, reaction progresses even when a temperature of the base is below 300 DEG C, and a GaAs monocrystal film which is extremely less in lattice failure and impurities was obtained. <IMAGE>
Description
SPECIFICATION
Process for growing GaAs monocrystal film
BACKGROUND OF THE INVENTION
Field of the Invention
The present invention relates to a process for growing a GaAs monocrystal film suitable for forming a monocrystal growing layer of GAAs in the order of a single molecular layer.
Description of the Prior Art
In the past, as a gas phase epitaxy technique for obtaining a film crystal of a semiconductor, an organic metal gas-phase growing process (hereinafter called "MO-CVD process") and a molecular beam epitaxy process (hereinafter called MBE process") have been known. However, where a compound semiconductor between Ill-group to V-group as in GaAs is grown by the
MO-CVD process, Ill-group and V-group elements as a source with a hydrogen gas as a carrier are simultaneously introduce for growth thereof by thermal cracking, and therefore the grown layer is poor in quality. There is a further disadvantage in that the order of the single molecular layer is difficult to control.
On the other hand the MBE process well known as a crystal growing process which utilizes a super-high vacuum employs physical adsorption as a first stage, and therefore, the quality of crystal obtained thereby is inferior to the gas-phase growing process which utilizes chemical reaction. When a compound semiconductor between Ill-group-V-group as in GaAs is grown, III- group and V-group elements are used as a source, the source itself being installed within a growing chamber. Because of this, controlling the emitted gas obtained by heating the source and the amount of vaporization, and supplying the source are difficult to make, and it is difficult to maintain the growth rate constant for a long period of time. Furthermore, a vacuum device such as discharge of vaporized material becomes complicated.Moreover, it is difficult to precisely control the stoichiometry of the compound semiconductor, and after all, there poses a disadvantage in that a crystal of high quality may not be obtained.
In view of the foregoing, the present inventors have previously proposed a semiconductor crystal growing process having a controllablility of a grown film layer of the single molecular layer order (see Japanese Patent Application Nos. 153977/1984 and 153978/1984 Specifications). This will be explained with reference to Fig. 5.
In Fig. 5, reference numeral 1 designates a growing tank, which is formed of metal such as stainless; 2, a gate valve; 3, an exhaust chamber for making the growing chamber 1 super-high vacuum; 4, 5, nozzles for introducing gaseous compounds of component elements of Ill-group and V-group of Ill-group-V-group compound semiconductors, for example; 6, 7, valves for opening and closing the nozzles 4, 5; 8, a gaseous compound containing a component element of Ill-group; 9, a gaseous compound containing a component element of V-group; and 10, a heater for heating the base, which is a tungsten (W) wire with quartz glass sealed therein, the wire or the like not shown.Reference numeral 11 designates a thermocouple for measuring the temperature; 12, a base for a compound semiconductor; and 13, a pressure gauge for measuring a vacuum degree within the growing tank.
The process for the expitaxial growth of GaAs molecular layers one by one on the base 12 is accomplished in the following procedure. That is, the gate valve 2 is opened, and the interior of the growing tank 1 is evacuated to the extent of 10-7 to 10-8 Pascal (hereinafter merely indicated at Pa) by the super-high vacuum evacuation device 3. Next, the GaAs base 12 is heated by means of the heater 10 to the extent of 300 to 800"C, and the valve 6 is opened to introduce TMG (trimethylgallium) 8 as a gas containing Ga into the tank for 0.5 to 10 seconds in the range that pressure within the growing tank is from 10-' to 10-7 Pa.Thereafter, after the valve 6 is closed to evacuate the gas within the growing tank 1, the valve 7 is opened to introduce AsH3 (arsine) 9 as a gas containing As into the tank for 2 to 200 seconds in the range that pressure is 10-1 to 107 Pa. Thereby, at least one molecular layer of GaAs may be grown on the base 12. The aforementioned steps of operation are repeated to successively grow single molecular layers, whereby the epitaxial grown layer of GaAs having the desired thickness may be grown with accuracy of a single molecular layer.
Incidentally, when in the process of crystal growth, the temperature of the crystal is increased, vacancies, atoms between lattices and the like are to present. In addition, impurities become taken in due to autodoping or the like, which is not preferable in view of growing crystals of high completeness. To avoid this, it is necessary to grow crystals without increasing the temperature. However, according to the previously proposed crystal growing process, the crystal growing temperature is relatively high, from 300 to 800 C, thus failing to obtain a single crystal of GaAs having a high completeness.
SUMMARY OF THE INVENTION
It is an object of the present invention to provide a process for growing a GaAs semiconductor monocrystal film having a high quality in the order of a single molecular layer, while overcoming the above-described problems.
According to the present invention, the processes previously proposed by the present inventors are further developed so that TEG and AsH3 are used as a source gas whereby they may be alternatively introduced into the growing tank under a predetermined pressure for a predetermined period of time to thereby obtain a highly pure GaAs monocrystal film at a low temperature below 300"C.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 is a structural view of a crystal growing apparatus according to one embodiment of the present invention;
Figure 2 is a graphic representation showing the relationship between the grown film thickness of a crystal manufactured by use of the apparatus shown in Fig. 1 and a temperature of a base;
Figure 3 is a graphic representation showing the relationship between the grown film thickness and the amount of introduction of TEG when the base temperature is 290"C; Figure 4 is a graphic representation showing the relationship between the density of impurities of the growth film with TEG and AsH3 as the source gas and the mobility as compared with a conventional molecular layer epitaxial film; and
Figure 5 is a structure view of a crystal growing apparatus previously proposed by the present inventors.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
One embodiment of the present invention will be described hereinafter.
Fig. 1 shows the structure of a molecular layer epitaxial growing apparatus according to one embodiment of the present invention. The same reference numerals in Fig. 1 as those of Fig. 5 indicate the same or corresponding parts in Fig. 5 with the exception that an infrared lamp 30 is used as a heating source, the lamp being provided within a lamp house 31 externally of a growing tank 1, and infrared rays emitted from the lamp house 31 are irradiated on a base 12 through a quartz glass 32 to heat the base 12 held by a susceptor 33.
This apparatus is used, and TEG (triethylgallium) 6 as a gas containing Ga is introduced under pressure of 10-6 to 10-2 Pa for 1 to 20 seconds and evacuated for 1 to 20 seconds. Then,
AsH3 (arsine) 9 as a gas containing As is introduced under pressure of 10-4 to 1 Pa for 1 to 200 seconds and then evacuated for 1 to 20 seconds. Thereby, a single molecular layer of
GaAs may be grown on the base 12. The above-described steps of operations are repeated to successively grow single molecular layers whereby a monocrystal grown film of GaAs having a desired thickness may be grown with accuracy of the single molecular layer.
Fig. 2 shows a grown film thickness in a direction of < 111 > B face of GaAs film per cycle at a temperature from 260"C to 350"C with a temperature of the base as a parameter, in which case TEG and AsH3 are used an an introducing gas. When the base temperature is 290"C, the
GaAs film per cycle was 3.2A corresponding to one molecular layer. The growth temperature of the aforesaid 260"C is a temperature lower by about 90"C than the minimum crystal growth temperature of 350"C in the crystal growing process relied upon a combination of TMG and
AsH3 previously proposed by the present inventors.
Fig. 3 shows a grown film thickness of GaAs per cycle, where the base temperature is 290"C, gas introducing pressure is 10-1 to 10-4 Pa, introducing time is 2 to 60 seconds, and evacuation time is 2 to 20 seconds, the amount of introduction of TEG per cycle being as a parameter.
As can be understood from Fig. 3, when the amount of TEG introduction per cycle increases, the grown film thickness becomes saturated. Accordingly, if the growing is made with the amount of gas introduction in excess of the saturated value, even if the amount of gas introduction should be slightly varied, the rowth of one molecular layer per cycle would be obtained positively. Therefore, the film thickness can be controlled with the accuracy of atom unit. The epitaxial grown layer of the thus obtained GaAs was examined by electron beam diffraction and X-ray diffraction, as the resuit of which was found that the layer was a film monocrystal having an extremely high completeness.
Fig. 4 shows the relationship between the density of impurities of a film submitted to the molecular layer epitaxial growing with TEG and AsH3 as a source gas and the mobility as compared with a conventional molecular layer epitaxial grown film formed from TMG and AsH3.
In Fig. 4, the curve indicated at A is a theoretically calculated value, the point indicated at B is a grown film with TEG and AsH3 as a source, and the point indicated at C is a conventional molecular layer epitaxial growing tank. As can be understood from this figure, in prior art, the density of impurities was high, 1015 to 1020cm-3, and the mobility was less than 100cm2 V-1
S-1, whereas in the present invention, the density of impurities was improved by 2 to 3 places, i.e. 10'5 to 10'7cm-3, and the mobility was a value close to the theoretical value, i.e., 360cm2
V-1 S-1. The thus obtained grown film was prepared under the experimental conditions such that pressure of TEG is 10-3 to 10-4 Pa, pressure of AsH3 is 10-' to 10-2 Pa, introduction time is between 2 and 60 seconds, and evacuation time is 20 to 20 seconds.It may be understood from Fig. 4 that the grown film according to the present invention is a particularly excellent highpurity mono-crystal as compared with that obtained by the conventional molecular layer epitaxial growth.
The density of impurities of thus obtained crystal was less than 1015cm-3, and the mobility was above 360cm2 V-1 S-1.
As described above, according to the present invention, crystals may be grown one by one, the stoichiometry can be easily fulfilled, and the base temperature is low. Therefore, it is possible to form a monocrystal having a good quality with a minimum lattice failure on the base.
Moreover, addition of impurities may be made one by one in layer, and therefore, an extremely sharp density distribution of impurities may be obtained, thus exhibiting excellent operation and effect in the manufacture of extremely high-speed transistors, integrated circuits, diode light emitting elements and the like.
Claims (6)
1. A process for growing a GaAs monocrystal film on a base by introducing a gas containing a crystal component element into a growing tank evacuated to vacuum from outside, characterized by evacuating the interior of said growing tank to a predetermined pressure, introducing
TEG (triethylgallium) into said growing tank under a predetermined pressure for a predetermined time, after evacuation of TEG introducing AsH3 (arsine) into said growing tank under a predetermined pressure for a predetermined time, and repeating the cycle for growing at least nearly one molecular layer to thereby grow a GaAs monocrystal film having a desired thickness with accuracy of a single molecular layer.
2. The process as set forth in Claim 1, wherein a heating source comprises an infrared lamp provided externally of the growing tank.
3. The process as set forth in Claim 1, wherein the average number of molecular layers per cycle of gas introduction is less than 2.
4. The process as set forth in Claim 1 or 2, wherein introduction pressure of TEG and AsH3 is 1 to 10--5 Pa, introduction time is 1 to 200 seconds, and evacuation time after said gas introduction is 1 to 20 seconds.
5. The process as set forth in Claim 1 to 3, wherein a temperature of the base is less than 300"C.
6. A process according to claim 1 and substantially as described herein with reference to
Figs. 1 to 4 of the accompanying drawings.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60101379A JPS61260622A (en) | 1985-05-15 | 1985-05-15 | Growth for gaas single crystal thin film |
Publications (3)
Publication Number | Publication Date |
---|---|
GB8612024D0 GB8612024D0 (en) | 1986-06-25 |
GB2190400A true GB2190400A (en) | 1987-11-18 |
GB2190400B GB2190400B (en) | 1990-10-17 |
Family
ID=14299154
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8612024A Expired - Fee Related GB2190400B (en) | 1985-05-15 | 1986-05-16 | Process for growing gaas monocrystal film |
Country Status (4)
Country | Link |
---|---|
JP (1) | JPS61260622A (en) |
DE (1) | DE3616358C2 (en) |
FR (1) | FR2582023B1 (en) |
GB (1) | GB2190400B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2200138A (en) * | 1984-07-26 | 1988-07-27 | Japan Res Dev Corp | Semiconductor crystal growth apparatus |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0657636B2 (en) * | 1985-05-29 | 1994-08-03 | 日本電信電話株式会社 | Compound semiconductor thin film formation method |
EP0297867B1 (en) * | 1987-07-01 | 1993-10-06 | Nec Corporation | A process for the growth of iii-v group compound semiconductor crystal on a si substrate |
JP2015525484A (en) * | 2012-06-18 | 2015-09-03 | アメリカ合衆国 | Plasma-assisted atomic layer epitaxy of cubic and hexagonal InN and its alloys with AlN at low temperatures |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1336910A (en) * | 1970-05-08 | 1973-11-14 | Western Electric Co | Formation of semiconductor films |
US3867202A (en) * | 1973-03-15 | 1975-02-18 | Sumitomo Chemical Co | Chemical vapor deposition for epitaxial growth |
GB2130189A (en) * | 1982-10-19 | 1984-05-31 | Secr Defence | Vapour deposition of films |
GB2162369A (en) * | 1984-07-26 | 1986-01-29 | Nishizawa Junichi | Apparatus for forming semiconductor crystal |
GB2163000A (en) * | 1984-07-26 | 1986-02-12 | Japan Res Dev Corp | Apparatus for forming crystal of semiconductor |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1900116C3 (en) * | 1969-01-02 | 1978-10-19 | Siemens Ag, 1000 Berlin Und 8000 Muenchen | Process for the production of high-purity monocrystalline layers consisting of silicon |
GB2162207B (en) * | 1984-07-26 | 1989-05-10 | Japan Res Dev Corp | Semiconductor crystal growth apparatus |
GB2162862B (en) * | 1984-07-26 | 1988-10-19 | Japan Res Dev Corp | A method of growing a thin film single crystalline semiconductor |
-
1985
- 1985-05-15 JP JP60101379A patent/JPS61260622A/en active Granted
-
1986
- 1986-05-15 DE DE3616358A patent/DE3616358C2/en not_active Expired - Fee Related
- 1986-05-15 FR FR8606988A patent/FR2582023B1/en not_active Expired - Fee Related
- 1986-05-16 GB GB8612024A patent/GB2190400B/en not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1336910A (en) * | 1970-05-08 | 1973-11-14 | Western Electric Co | Formation of semiconductor films |
US3867202A (en) * | 1973-03-15 | 1975-02-18 | Sumitomo Chemical Co | Chemical vapor deposition for epitaxial growth |
GB2130189A (en) * | 1982-10-19 | 1984-05-31 | Secr Defence | Vapour deposition of films |
GB2162369A (en) * | 1984-07-26 | 1986-01-29 | Nishizawa Junichi | Apparatus for forming semiconductor crystal |
GB2163000A (en) * | 1984-07-26 | 1986-02-12 | Japan Res Dev Corp | Apparatus for forming crystal of semiconductor |
Non-Patent Citations (1)
Title |
---|
CHEMISTRY AND INDUSTRY, 15 APRIL 1985 PAGES 247 TO 251 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2200138A (en) * | 1984-07-26 | 1988-07-27 | Japan Res Dev Corp | Semiconductor crystal growth apparatus |
GB2200138B (en) * | 1984-07-26 | 1989-05-10 | Japan Res Dev Corp | Semiconductor crystal growth apparatus |
Also Published As
Publication number | Publication date |
---|---|
JPH0556650B2 (en) | 1993-08-20 |
FR2582023B1 (en) | 1994-04-15 |
GB2190400B (en) | 1990-10-17 |
JPS61260622A (en) | 1986-11-18 |
DE3616358C2 (en) | 1996-02-15 |
DE3616358A1 (en) | 1986-11-20 |
FR2582023A1 (en) | 1986-11-21 |
GB8612024D0 (en) | 1986-06-25 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
732 | Registration of transactions, instruments or events in the register (sect. 32/1977) | ||
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 20040516 |