CN1936119A - InP monocrystal ingot annealing treatment method - Google Patents
InP monocrystal ingot annealing treatment method Download PDFInfo
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- CN1936119A CN1936119A CN 200510086482 CN200510086482A CN1936119A CN 1936119 A CN1936119 A CN 1936119A CN 200510086482 CN200510086482 CN 200510086482 CN 200510086482 A CN200510086482 A CN 200510086482A CN 1936119 A CN1936119 A CN 1936119A
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Abstract
The invention relates to an InP single crystal ingot annealing treatment method that includes the following steps: washing the surface of InP single crystal by deionized water to remove boric anhydride; scrubbing by organic solvent, washing by deionized water and drying; preparing quartz tube and sealed froth and washing after dipping by aqua regia, drying; directly putting the crystal into silica tube and putting red phosphorus; sealing froth and vacuuming, sintering by oxyhydrogen flame and sealing; putting the silica tube with crystal into annealing furnace to finish InP single crystal ingot annealing process. The invention could improve the quality of crystal.
Description
Technical field
The invention belongs to microelectronics and photoelectron compound semiconductor materials preparing technical field, be that relevant anneal reduces the thermal stresses in indium phosphorus (InP) monocrystalline and improves the inhomogeneity technology of crystalline electricity, be meant a kind of InP monocrystal ingot annealing treatment method especially.
Background technology
The InP monocrystalline is a kind of important substrate material of making microwave device, photoelectronic device for optical fiber communication etc.The InP monocrystalline that grows need cut into standard-sized wafer, passes through the courses of processing such as chamfering, grinding, polishing, cleaning then, becomes the commodity wafer and uses for the user.In the whole course of processing, keep wafer physical strength, avoid cracked for raising manufacture a finished product rate, to reduce cost be vital.At present, lack relevant crystal annealing and handle, reduce the inhomogeneity robust techniques technology of electricity of residual heat stress and raising material.
Summary of the invention
The objective of the invention is to, a kind of InP monocrystal ingot annealing treatment method is provided, exist very high residual heat stress among the compound semiconductor single crystal InP that grows with solution, as easy as rolling off a log cause crystal in cutting process, to ftracture and wafer cracked in grinding, polishing, cleaning and use, improve the crystalline quality.
Another object of the present invention is to, a kind of InP monocrystal ingot annealing treatment method is provided,, improve the homogeneity of crystalline electrical properties to eliminate the inhomogeneous of crystalline Impurity Distribution.
A kind of InP monocrystal ingot annealing treatment method of the present invention is characterized in that, comprises the steps:
Step 1:, remove residual boron oxide with the InP single-crystal surface washed with de-ionized water that grows;
Step 2: clean with organic solvent then, stand-by with drying behind the deionized water rinsing;
Step 3: prepare silica tube and Feng Pao, it is clean to soak the back deionized water rinsing with chloroazotic acid, dries stand-by;
Step 4: crystal is directly put into silica tube, put into red phosphorus simultaneously;
Step 5: put envelope bubble back then and vacuumize, seal with the oxyhydrogen flame sintering with mechanical pump;
Step 6: the crystalline silica tube will be housed put into the annealing furnace annealing, and finish InP single crystal rod anneal.
Wherein the organic solvent of step 2 is acetone or alcohol.
Wherein the internal diameter of the silica tube of step 3 and envelope bubble is greater than the crystalline diameter.
Wherein step 3 is 2 hours with the time that chloroazotic acid soaks.
Wherein the pressure of the phosphorous vapor of silica tube is 60mbar in the step 4,200 milligrams.
Wherein the annealing in the step 6 is heated by following speed: room temperature-500 ℃, 100 ℃/hour; 500 ℃-800 ℃, 60 ℃/hour; 800 ℃-950 ℃, 30 ℃/hour; 950 ℃ of constant temperature 5 hours; Then by following speed cooling: 950 ℃-800 ℃, 30 ℃/hour; 800 ℃-500 ℃, 60 ℃/hour; 500 ℃-room temperature, 100 ℃/hour.
Embodiment
A kind of InP monocrystal ingot annealing treatment method of the present invention is characterized in that, comprises the steps:
Step 1: the InP monocrystalline that grows was soaked 4 hours with deionized water, remove residual boron oxide;
Step 2: clean with organic solvent then, this organic solvent is acetone or alcohol, and is stand-by with drying behind the deionized water rinsing;
Step 3: prepare the envelope bubble that silica tube and silica tube seal usefulness, clean with acetone or alcohol, it is clean so to soak after 2 hours deionized water rinsing with chloroazotic acid, dries stand-by;
Step 4: crystal is directly put into silica tube, put into 200 milligrams in red phosphorus simultaneously;
Step 5: put envelope bubble back then and vacuumize, seal with the oxyhydrogen flame sintering with mechanical pump;
Step 6: the crystalline silica tube will be housed put into the annealing furnace annealing, and wherein anneal and heat: room temperature-500 ℃, 100 ℃/hour by following speed; 500 ℃-800 ℃, 60 ℃/hour; 800 ℃-950 ℃, 30 ℃/hour; 950 ℃ of constant temperature 5 hours; Then by following speed cooling: 950 ℃-800 ℃, 30 ℃/hour; 800 ℃-500 ℃, 60 ℃/hour; 500 ℃-room temperature, 100 ℃/hour, finish InP single crystal rod anneal.
Embodiment
With high-pressure liquid encapsulation pulling method grow (a 100) crystal orientation, mix sulphur InP monocrystalline, diameter is 58 millimeters, and is long 150 millimeters, weight is 1380 grams, prepares to carry out anneal.At first the InP single crystal rod that grows was soaked 4 hours with deionized water, remove the boron oxide that remains in the surface.Use organic solvent (acetone and alcohol) scrub surface then, stand-by with drying behind the deionized water rinsing.Preparing an external diameter is 90 millimeters, 3 millimeters of wall thickness, and length is 600 millimeters, the silica tube of an end closure and an external diameter are 84 millimeters, high 150 millimeters quartz envelope bubble (quartz crucible).With chloroazotic acid soak silica tube and envelope bubble after 2 hours deionized water rinsing clean, dry stand-by.Crystal is directly put into silica tube, put into a certain amount of red phosphorus simultaneously,, keep the pressure of about 60mbar, generally about 200 milligrams according to the Calculation of Effective Volume of silica tube.To seal port that bubble is placed on silica tube then, vacuumize with mechanical pump after connecting the interface of pipeline, reach 10
-2Promptly seal behind the mmHg with the oxyhydrogen flame sintering.
Put into the burner hearth of annealing furnace with the crystalline silica tube is housed, go up so that be incubated with insulating brick is stifled the port, and the temperature of burner hearth is debugged in advance and need be set up the above flat-temperature zone of 200 millimeters long, and monocrystalline is in the flat-temperature zone.Heat by following speed: room temperature-500 ℃, 100 ℃/hour; 500 ℃-800 ℃, 60 ℃/hour; 800 ℃-950 ℃, 30 ℃/hour.950 ℃ of constant temperature 5 hours.Then by following speed cooling: 950 ℃-800 ℃, 30 ℃/hour; 800 ℃-500 ℃, 60 ℃/hour; 500 ℃-room temperature, 100 ℃/hour.
Silica tube is taken out, cut an osculum at a slow speed earlier, cut fast again after waiting to exit with cutting machine.Prepare slice processing after taking out crystal.
The flat-temperature zone length of annealing furnace should be greater than crystalline length, to guarantee the annealed effect.Generally should use the process furnace of at least 3 warm areas.
Impurity Distribution is inhomogeneous in the InP monocrystalline of primordial condition, accumulates in (as the iron contamination in the semi-insulating inp) around the dislocation, causes the resistivity of material and carrier concentration profile inhomogeneous.Need by annealing, the diffusion that produces impurity atoms activates, and makes Impurity Distribution even, thereby improves the electricity homogeneity of material.
In constant, the equally distributed High Temperature Furnaces Heating Apparatus of temperature, the InP monocrystalline is carried out long term annealing and handle, can effectively reduce the residual heat stress in the crystal.During annealing, crystal is enclosed in the silica tube, and the phosphorous vapor that also needs in the pipe to keep certain is pressed to prevent crystal understanding.Need in annealing process that strict control crystalline heats up, cooling rate, avoid producing defectives such as dislocation owing to warming and cooling rate is too fast.
Can effectively eliminate residual heat stress in the crystal by anneal, avoid the crystalline cutting cracked, significantly improve crystalline electricity homogeneity, improve the crystalline quality.
Claims (6)
1, a kind of InP monocrystal ingot annealing treatment method is characterized in that, comprises the steps:
Step 1:, remove residual boron oxide with the InP single-crystal surface washed with de-ionized water that grows;
Step 2: clean with organic solvent then, stand-by with drying behind the deionized water rinsing;
Step 3: prepare silica tube and Feng Pao, it is clean to soak the back deionized water rinsing with chloroazotic acid, dries stand-by;
Step 4: crystal is directly put into silica tube, put into red phosphorus simultaneously;
Step 5: put envelope bubble back then and vacuumize, seal with the oxyhydrogen flame sintering with mechanical pump;
Step 6: the crystalline silica tube will be housed put into the annealing furnace annealing, and finish InP single crystal rod anneal.
2, InP monocrystal ingot annealing treatment method according to claim 1 is characterized in that, wherein the organic solvent of step 2 is acetone or alcohol.
3, InP monocrystal ingot annealing treatment method according to claim 1 is characterized in that, wherein the internal diameter of the silica tube of step 3 and envelope bubble is greater than the crystalline diameter.
4, InP monocrystal ingot annealing treatment method according to claim 1 is characterized in that, wherein step 3 is 2 hours with the time that chloroazotic acid soaks.
5, InP monocrystal ingot annealing treatment method according to claim 1 is characterized in that, wherein the pressure of the phosphorous vapor of silica tube is 60mbar in the step 4,200 milligrams.
6, InP monocrystal ingot annealing treatment method according to claim 1 is characterized in that, wherein the annealing in the step 6 is heated by following speed: room temperature-500 ℃, 100 ℃/hour; 500 ℃-800 ℃, 60 ℃/hour; 800 ℃-950 ℃, 30 ℃/hour; 950 ℃ of constant temperature 5 hours; Then by following speed cooling: 950 ℃-800 ℃, 30 ℃/hour; 800 ℃-500 ℃, 60 ℃/hour; 500 ℃-room temperature, 100 ℃/hour.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100864828A CN100387761C (en) | 2005-09-22 | 2005-09-22 | InP monocrystal ingot annealing treatment method |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100864828A CN100387761C (en) | 2005-09-22 | 2005-09-22 | InP monocrystal ingot annealing treatment method |
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| CN1936119A true CN1936119A (en) | 2007-03-28 |
| CN100387761C CN100387761C (en) | 2008-05-14 |
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| CNB2005100864828A Expired - Fee Related CN100387761C (en) | 2005-09-22 | 2005-09-22 | InP monocrystal ingot annealing treatment method |
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Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102040204B (en) * | 2009-10-16 | 2013-01-16 | 北京有色金属研究总院 | Method for casting ingots by using gallium phosphide polycrystal |
| CN103361735A (en) * | 2012-03-26 | 2013-10-23 | 北京通美晶体技术有限公司 | IIIA-VA group semiconductor monocrystal substrate and preparation method thereof |
| CN105408528A (en) * | 2013-03-27 | 2016-03-16 | 北京通美晶体技术有限公司 | Controllable oxygen concentration in semiconductor substrate |
| CN105603534A (en) * | 2016-02-26 | 2016-05-25 | 吕远芳 | Germanium crystal stress elimination method |
| CN106400102A (en) * | 2016-10-26 | 2017-02-15 | 北京鼎泰芯源科技发展有限公司 | Growth equipment and method thereof capable of achieving online annealing of single crystal |
| CN107675262A (en) * | 2017-11-10 | 2018-02-09 | 北京鼎泰芯源科技发展有限公司 | A kind of method for annealing for mixing iron indium phosphide single crystal wafer |
| CN107829142A (en) * | 2017-11-10 | 2018-03-23 | 北京鼎泰芯源科技发展有限公司 | The method for eliminating InP chip microdefects |
| CN107829141A (en) * | 2017-11-10 | 2018-03-23 | 北京鼎泰芯源科技发展有限公司 | The circulation utilization method of rich indium indium phosphide polycrystal material |
| CN109112637A (en) * | 2018-09-26 | 2019-01-01 | 汉能新材料科技有限公司 | A kind of method for annealing of gallium arsenide and obtained gallium arsenide wafer |
| CN109111097A (en) * | 2018-09-28 | 2019-01-01 | 广州宏晟光电科技股份有限公司 | A kind of glass optical fiber drawing furnace |
| CN111263833A (en) * | 2018-02-23 | 2020-06-09 | 住友电气工业株式会社 | Indium phosphide crystal substrate |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JPS61117198A (en) * | 1984-11-13 | 1986-06-04 | Nippon Telegr & Teleph Corp <Ntt> | Melt for growth of inp single crystal and method for using said melt |
| JPS6385099A (en) * | 1986-09-27 | 1988-04-15 | Sumitomo Electric Ind Ltd | Production of indium phosphide single crystal |
| JPH0632699A (en) * | 1992-07-14 | 1994-02-08 | Japan Energy Corp | Production of semi-insulating inp single crystal |
| JPH08175899A (en) * | 1994-12-21 | 1996-07-09 | Japan Energy Corp | Production of semi-insulating indium phosphide single crystal |
| US6455385B1 (en) * | 1998-01-07 | 2002-09-24 | Advanced Micro Devices, Inc. | Semiconductor fabrication with multiple low dose implant |
-
2005
- 2005-09-22 CN CNB2005100864828A patent/CN100387761C/en not_active Expired - Fee Related
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102040204B (en) * | 2009-10-16 | 2013-01-16 | 北京有色金属研究总院 | Method for casting ingots by using gallium phosphide polycrystal |
| CN103361735A (en) * | 2012-03-26 | 2013-10-23 | 北京通美晶体技术有限公司 | IIIA-VA group semiconductor monocrystal substrate and preparation method thereof |
| CN105408528A (en) * | 2013-03-27 | 2016-03-16 | 北京通美晶体技术有限公司 | Controllable oxygen concentration in semiconductor substrate |
| CN105603534A (en) * | 2016-02-26 | 2016-05-25 | 吕远芳 | Germanium crystal stress elimination method |
| CN106400102A (en) * | 2016-10-26 | 2017-02-15 | 北京鼎泰芯源科技发展有限公司 | Growth equipment and method thereof capable of achieving online annealing of single crystal |
| CN106400102B (en) * | 2016-10-26 | 2019-06-28 | 珠海鼎泰芯源晶体有限公司 | A kind of growth apparatus and its method of achievable monocrystalline online annealing |
| CN107829142A (en) * | 2017-11-10 | 2018-03-23 | 北京鼎泰芯源科技发展有限公司 | The method for eliminating InP chip microdefects |
| CN107829141A (en) * | 2017-11-10 | 2018-03-23 | 北京鼎泰芯源科技发展有限公司 | The circulation utilization method of rich indium indium phosphide polycrystal material |
| CN107675262A (en) * | 2017-11-10 | 2018-02-09 | 北京鼎泰芯源科技发展有限公司 | A kind of method for annealing for mixing iron indium phosphide single crystal wafer |
| CN111263833A (en) * | 2018-02-23 | 2020-06-09 | 住友电气工业株式会社 | Indium phosphide crystal substrate |
| CN111263833B (en) * | 2018-02-23 | 2020-10-16 | 住友电气工业株式会社 | Indium phosphide crystal substrate |
| CN109112637A (en) * | 2018-09-26 | 2019-01-01 | 汉能新材料科技有限公司 | A kind of method for annealing of gallium arsenide and obtained gallium arsenide wafer |
| CN109111097A (en) * | 2018-09-28 | 2019-01-01 | 广州宏晟光电科技股份有限公司 | A kind of glass optical fiber drawing furnace |
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