JPS63297211A - Si-b alloy dopant material for production of si single crystal by pulling up method - Google Patents
Si-b alloy dopant material for production of si single crystal by pulling up methodInfo
- Publication number
- JPS63297211A JPS63297211A JP13398587A JP13398587A JPS63297211A JP S63297211 A JPS63297211 A JP S63297211A JP 13398587 A JP13398587 A JP 13398587A JP 13398587 A JP13398587 A JP 13398587A JP S63297211 A JPS63297211 A JP S63297211A
- Authority
- JP
- Japan
- Prior art keywords
- single crystal
- dopant material
- alloy
- pulling
- production
- 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
Links
- 239000002019 doping agent Substances 0.000 title claims abstract description 21
- 239000013078 crystal Substances 0.000 title claims abstract description 20
- 239000000463 material Substances 0.000 title claims abstract description 20
- 229910045601 alloy Inorganic materials 0.000 title claims abstract description 10
- 239000000956 alloy Substances 0.000 title claims abstract description 10
- 238000000034 method Methods 0.000 title claims abstract description 6
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 5
- 229910008423 Si—B Inorganic materials 0.000 claims abstract description 10
- 238000005204 segregation Methods 0.000 abstract description 6
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 4
- 239000000155 melt Substances 0.000 description 4
- 229910015900 BF3 Inorganic materials 0.000 description 3
- 235000012431 wafers Nutrition 0.000 description 3
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000003908 quality control method Methods 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910000521 B alloy Inorganic materials 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005372 isotope separation Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 1
Landscapes
- Crystals, And After-Treatments Of Crystals (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
この発明は、引上げ法(二より製造されたSi単結晶ロ
ッドにおけるドープBの偏析を著しく低減することがで
きるSi−B合金ドーパント材(−関するものである。Detailed Description of the Invention [Industrial Application Field] This invention provides a Si-B alloy dopant material (- It is related to
一般(−1Si単結晶ロツドは、多結晶Stとドーパン
ト材としてのSi−B合金とを石英るつぼで溶解して融
液とした後、所定の結晶方位をもった種結晶の先端を前
記融液につけ、前記るつぼおよび種結晶をそれぞれ所定
の回転速度で回転させながら、前記種結晶を所定の速度
で引上げることによって製造されている。General (-1Si single crystal rods are produced by melting polycrystalline St and a Si-B alloy as a dopant material into a melt in a quartz crucible, and then inserting the tip of a seed crystal with a predetermined crystal orientation into the melt. It is produced by pulling up the seed crystal at a predetermined speed while rotating the crucible and the seed crystal at predetermined rotational speeds.
しかし、上記の従来S1単結晶ロツドにおいては、ドー
プBが偏析し、このため例えばロッドの上部、中間部、
および下部のB濃度(ニバラッキが生じ、このようなり
9度(二局部的バラツキのあるロッドよりスライスされ
たウェハでは、ウェハ相互の電気特性、特に抵抗値(−
バラツキが生じるよう(二なり、歩留りが低下するばか
りでなく、品質管理の面からも問題がある。However, in the above-mentioned conventional S1 single crystal rod, the dope B segregates, so that, for example, the upper part, the middle part of the rod,
and the B concentration at the bottom (nivaracchi occurs, and in a wafer sliced from a rod with two local variations like this, the electric properties of the wafers, especially the resistance value (-
If variations occur, not only will the yield decrease, but there will also be problems in terms of quality control.
そこで、本発明者等は、上述のような観点から。 Therefore, the inventors of the present invention, from the above-mentioned viewpoint.
ドープBの偏析がないSi単結晶ロッドを製造丁べく、
特にSi−B合金ドーパント材(二着目し、研究を行な
った結果、従来のSi−B合金ドーパント材のBは天然
Bからなり、この天然Bは、重量比で約80:20の割
合の11BとIOBの2種の同位元素で構成されている
が、このような同位元素 Bと同10Bの割合を、11
Bが95%以上を占め、一方10Bを5%以下とした割
合(以上重量%、以下%は重量%を示す)に代えると、
引上げ法により製造されたSi単結晶ロッド(二おける
ドープBの偏析がなくなり、均一な特性をもったウェル
が得られるようになるという知゛見を得たのである。In order to manufacture Si single crystal rods without segregation of dope B,
In particular, Si-B alloy dopant materials (second focus and research have shown that B in conventional Si-B alloy dopant materials consists of natural B, and this natural B is 11B in a weight ratio of approximately 80:20). It is composed of two types of isotopes, B and IOB, and the ratio of these isotopes B and IOB is 11
B accounts for 95% or more, while 10B accounts for 5% or less (weight% above, below % indicates weight%):
It was discovered that the segregation of dope B in Si single crystal rods produced by the pulling method was eliminated, and wells with uniform properties could be obtained.
この発明は、上記知見(=もとづいてなされたものであ
って、同位元素である Bの割合が95%以上を占め、
一方同10 Bの割合が5%以下であるBで構成した。This invention was made based on the above knowledge (= the proportion of the isotope B accounts for 95% or more,
On the other hand, it was composed of B in which the proportion of 10 B was 5% or less.
引上げ法によるS1単結晶製造用Si−B合金ドーパン
ト材に特徴を有するものである。This is a characteristic feature of the Si-B alloy dopant material for producing S1 single crystals by the pulling method.
なお、11Bと10 Bの2種の同位元素からなるB成
分(:おいては、11Bの割合が95%未満では、必然
的にIOBの割合が5%を越えて多くなり、このような
割合の11BとIOBで構成されたB含有のSi−Bド
ーパント材では、上記のようにドープBの偏析を効果的
に抑制することができないことから、Si−B合金ドー
パント材のBにおける同位元素である11BとIOBの
割合を、11B : 95%以上、10B : 5%以
下と定めたのである。In addition, in the B component (:) consisting of two isotopes, 11B and 10B, if the proportion of 11B is less than 95%, the proportion of IOB will inevitably increase to more than 5%, and such a proportion In the B-containing Si-B dopant material composed of 11B and IOB, the segregation of dope B cannot be effectively suppressed as described above. The ratio of 11B and IOB was set as 95% or more for 11B and 5% or less for 10B.
つぎに、この発明のドーパント材を実施例により具体的
(二説明する。Next, the dopant material of the present invention will be specifically explained using Examples.
まず、アニソールを用い、三弗化はう素を化学交換蒸留
する同位元素分離法により、それぞれ第1表(−示され
る割合の11BとIOBからなる三弗化はう素を製造し
、これらの三弗化はう素から通常の化学的手段により金
属Bを形成し、これをSiに0.1%の割合で合金化す
ることにより本発明ドーパント材1〜3および比較ドー
プくント材1〜3をそれぞれ製造した。First, boron trifluoride consisting of 11B and IOB in the proportions shown in Table 1 (-) was produced by isotope separation method of chemical exchange distillation of boron trifluoride using anisole. Dopant materials 1 to 3 of the present invention and comparative dopant materials 1 to 3 are prepared by forming metal B from boron trifluoride by conventional chemical means and alloying it with Si at a ratio of 0.1%. 3 were produced respectively.
なお、比較ドーパント材1〜3は、いずれも11’Hの
割合がこの発明の範囲から低い方に外れたものであって
、このうちの比較ドープくント材1が従来ドーパント材
に相当するものである。In addition, comparative dopant materials 1 to 3 all have a ratio of 11'H that is lower than the range of the present invention, and among these, comparative dopant material 1 corresponds to the conventional dopant material. It is.
第 1 表
つぎに、この結果得られた各種のドーパント材を、多結
晶Si:30Kf、 ドーパント材: 0.49の割
合で内径:約350Mの石英るつぼ内(二人れ、これを
Ar雰囲気中で温度:1420℃に加熱し、溶解して融
液となし、るつぼをl Q r pmで回転させ、一方
前記融液につけた種結晶を2Orpmで回転させながら
、かつ前記種結晶を1. s mm 7分の速さで引上
げることによって、直径:約130 ran X長さ:
900+wの寸法をもったSi単結晶ロッドをそれぞれ
製造した。Table 1 Next, the various dopant materials obtained as a result were placed in a quartz crucible with an inner diameter of about 350 M (two people placed it in an Ar atmosphere) at a ratio of polycrystalline Si: 30Kf and dopant material: 0.49. The crucible was heated to a temperature of 1420° C. to form a melt, and the crucible was rotated at l Q r pm, while the seed crystal attached to the melt was rotated at 2 Orpm, and the seed crystal was heated for 1.s. By pulling at a speed of mm 7 minutes, diameter: approximately 130 ran x length:
Si single crystal rods with dimensions of 900+w were each manufactured.
ついで、この結果得られた各種のSi単結晶ロッドにつ
いて、上部(上端から50m内側の個所)、中央部、お
よび下部(下端から50mm+内側の個所)におけるB
濃度および比抵抗をそれぞれ測定した。Next, for the various Si single crystal rods obtained as a result, B at the upper part (50 m inside from the upper end), the center part, and the lower part (50 mm + inside from the lower end)
Concentration and specific resistance were measured respectively.
これらの測定結果を第1表1=示した。The results of these measurements are shown in Table 1.
第1表に示される結果から1本発明ドーパント材1〜3
を用いて製造されたSi単結晶ロッドにおいては、B濃
度の偏析がきわめて少なく、ロッド全体−二亘ってほぼ
一定の比抵抗を示すのに対して、11Bの割合が95%
未満の比較ドーパント材1〜3を用いた場合には、ドー
プBの偏析防止効果が十分でなく、比抵抗のバラツキも
相対的に大きいことが明らかである。From the results shown in Table 1, the dopant materials 1 to 3 of the present invention
In the Si single crystal rod manufactured using 11B, the segregation of B concentration is extremely small and the resistivity is almost constant throughout the rod, whereas the proportion of 11B is 95%.
It is clear that when comparative dopant materials 1 to 3 of less than
上述のように、この発明の5L−B合金ドーパント材(
二よれば、B濃度の偏析のきわめて少ないSt単結晶ロ
ッドを製造することができ、したがってこれをスライス
したウェハにおいては電気特性が均質化し、この結果歩
留が向上し、品質管理が容易となるなど工業上有用な効
果がもたらされるのである。As mentioned above, the 5L-B alloy dopant material (
According to 2, it is possible to manufacture St single crystal rods with extremely low B concentration segregation, and therefore wafers sliced from this rod have homogeneous electrical properties, resulting in improved yield and easier quality control. Industrially useful effects such as these are brought about.
Claims (1)
合が95重量%以上を占め、一方同^1^0Bの割合が
5重量%以下であるBで構成したことを特徴とする引上
げ法によるSi単結晶製造用Si−B合金ドーパント材
。A pulling method characterized in that the Si-B alloy is composed of B in which the proportion of the isotope ^1^1B is 95% by weight or more, while the proportion of the isotope ^1^0B is 5% by weight or less. Si-B alloy dopant material for Si single crystal production.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13398587A JPH085663B2 (en) | 1987-05-29 | 1987-05-29 | Si-B alloy dopant material for producing Si single crystal by pulling method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13398587A JPH085663B2 (en) | 1987-05-29 | 1987-05-29 | Si-B alloy dopant material for producing Si single crystal by pulling method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63297211A true JPS63297211A (en) | 1988-12-05 |
JPH085663B2 JPH085663B2 (en) | 1996-01-24 |
Family
ID=15117689
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13398587A Expired - Lifetime JPH085663B2 (en) | 1987-05-29 | 1987-05-29 | Si-B alloy dopant material for producing Si single crystal by pulling method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH085663B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001006041A1 (en) * | 1999-07-19 | 2001-01-25 | Topsil Semiconductor Materials A/S | Method and apparatus for production of a doped feed rod by ion implantation |
JP2002284518A (en) * | 2001-03-27 | 2002-10-03 | Japan Science & Technology Corp | Boron crystal, boron compound crystal, and method for manufacturing them |
-
1987
- 1987-05-29 JP JP13398587A patent/JPH085663B2/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001006041A1 (en) * | 1999-07-19 | 2001-01-25 | Topsil Semiconductor Materials A/S | Method and apparatus for production of a doped feed rod by ion implantation |
JP2002284518A (en) * | 2001-03-27 | 2002-10-03 | Japan Science & Technology Corp | Boron crystal, boron compound crystal, and method for manufacturing them |
Also Published As
Publication number | Publication date |
---|---|
JPH085663B2 (en) | 1996-01-24 |
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