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JP2010040588A - Silicon wafer - Google Patents

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JP2010040588A
JP2010040588A JP2008198681A JP2008198681A JP2010040588A JP 2010040588 A JP2010040588 A JP 2010040588A JP 2008198681 A JP2008198681 A JP 2008198681A JP 2008198681 A JP2008198681 A JP 2008198681A JP 2010040588 A JP2010040588 A JP 2010040588A
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oxygen concentration
silicon wafer
solid solution
region
silicon
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Inventor
Hiromichi Isogai
宏道 磯貝
Takeshi Senda
剛士 仙田
Eiji Toyoda
英二 豊田
Kumiko Murayama
久美子 村山
Koji Araki
浩司 荒木
Tatsuhiko Aoki
竜彦 青木
Haruo Sudo
治生 須藤
Yoichiro Mochizuki
陽一郎 望月
Akihiko Kobayashi
昭彦 小林
Shinrin Fu
森林 符
Koji Sensai
宏治 泉妻
Susumu Maeda
進 前田
Kazuhiko Kashima
一日児 鹿島
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Coorstek KK
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Covalent Materials Corp
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Priority to JP2008198681A priority Critical patent/JP2010040588A/en
Priority to CN 200910157497 priority patent/CN101638807B/en
Priority to US12/512,492 priority patent/US8476149B2/en
Priority to KR1020090070845A priority patent/KR20100014191A/en
Priority to TW098125986A priority patent/TWI410539B/en
Publication of JP2010040588A publication Critical patent/JP2010040588A/en
Pending legal-status Critical Current

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Abstract

<P>PROBLEM TO BE SOLVED: To provide a silicon wafer that is made free from a Grown-in defect, has high gettering effect, prevents BMD from being deposited in a device active region, and is improved in thermal strength of the device active region. <P>SOLUTION: The silicon wafer has a high-oxygen-concentration region where a solid solution oxygen concentration is ≥0.7×10<SP>18</SP>atoms/cm<SP>3</SP>in a no-defect region (DZ layer) 12 including at least the device active region of the silicon wafer 10, and contains interstitial silicon 14 in the no-defect region 12 in a supersaturation state. <P>COPYRIGHT: (C)2010,JPO&INPIT

Description

本発明は、半導体デバイスの製造に使用されるシリコンウェーハに関する。   The present invention relates to a silicon wafer used for manufacturing a semiconductor device.

近年の半導体デバイスの高集積化に伴い、その基板として用いられるシリコンウェーハに対する品質要求が厳しくなってきている。特に、シリコンウェーハのデバイス活性領域におけるGrown−in欠陥の無欠陥化や、高いゲッタリング効果を備えることが強く要求されている。   With the recent high integration of semiconductor devices, quality requirements for silicon wafers used as substrates have become severe. In particular, there is a strong demand for eliminating a grown-in defect in a device active region of a silicon wafer and providing a high gettering effect.

これらの要求に対し、格子間シリコン型点欠陥の凝集体及び空孔型点欠陥の凝集体が存在しないパーフェクト領域に属する侵入型転位を形成し得る最低の格子間シリコン濃度未満の領域を含み、かつ酸素濃度が0.97×1018〜1.4×1018atoms/cmであるシリコン単結晶インゴットを引上げ、前記インゴットから切出されたシリコンウェーハをシラン化合物と一酸化二窒素の混合ガス雰囲気下、700〜900℃で30〜120分間保持する技術が知られている(例えば、特許文献1)。 In response to these requirements, including a region below the lowest interstitial silicon concentration capable of forming interstitial dislocations belonging to a perfect region where there are no interstitial silicon type point defect aggregates and no vacancy type point defect aggregates, A silicon single crystal ingot having an oxygen concentration of 0.97 × 10 18 to 1.4 × 10 18 atoms / cm 3 is pulled up, and the silicon wafer cut out from the ingot is mixed with a silane compound and dinitrogen monoxide. A technique of holding at 700 to 900 ° C. for 30 to 120 minutes in an atmosphere is known (for example, Patent Document 1).

また、これらの要求に加え、基板の機械的強度を確保したシリコン基板を得ることを目的として、1100℃以上かつ特定の関係式で示される温度T未満の温度に加熱して、少なくとも10分間以上の熱処理を行って表面層の固溶酸素を外方拡散させる技術が知られている(例えば、特許文献2)。   In addition to these requirements, for the purpose of obtaining a silicon substrate that ensures the mechanical strength of the substrate, it is heated to a temperature of 1100 ° C. or higher and lower than the temperature T indicated by the specific relational expression for at least 10 minutes or longer. A technique is known in which solid solution oxygen in the surface layer is diffused outward by performing the heat treatment (for example, Patent Document 2).

更に、近年において、上記要求を備え、かつ、シリコンウェーハを高生産性でかつ簡単に作製する技術として、シリコンウェーハに、急速加熱・急速冷却熱処理(RTP:Rapid Thermal Process)を施す技術が知られている(例えば、特許文献3)。
特開2002−134513号公報 特開平5−291097号公報 特開2003−224130号公報
Further, in recent years, as a technique for easily producing a silicon wafer with the above requirements and with high productivity, a technique for subjecting a silicon wafer to rapid heating / cooling heat treatment (RTP: Rapid Thermal Process) is known. (For example, Patent Document 3).
JP 2002-134513 A Japanese Patent Application Laid-Open No. 5-291997 JP 2003-224130 A

しかしながら、特許文献1から3に記載の技術は、デバイス活性領域におけるGrown−in欠陥の無欠陥化や、高いゲッタリング効果を得ることを目的としており、デバイス活性領域におけるBMDの析出を考慮したものではない。このBMDは、通常、デバイス活性領域以外のバルク領域に析出された場合には、重金属等に対するゲッタリング効果を備えているため有効であるが、デバイス活性領域内に析出された場合には、デバイス歩留を低下させる要因となる。ましてや、酸素濃度が高いシリコンウェーハは、バルク領域におけるBMDの析出密度が高くなる一方で、デバイス活性領域においてもBMDの析出密度が高くなるという問題がある。   However, the techniques described in Patent Documents 1 to 3 are intended to eliminate a grown-in defect in the device active region and to obtain a high gettering effect, and take into account the precipitation of BMD in the device active region. is not. Normally, this BMD is effective when it is deposited in a bulk region other than the device active region because it has a gettering effect on heavy metals or the like. It becomes a factor to reduce the yield. In addition, a silicon wafer having a high oxygen concentration has a problem that the BMD precipitation density in the bulk region increases, while the BMD precipitation density also increases in the device active region.

また、特許文献1から3に記載の技術におけるシリコンウェーハの熱処理は、デバイス活性領域におけるGrown−in欠陥の無欠陥化や、高いゲッタリング効果を得るために有効な手段であるが、これらの熱処理によって、少なからずとも、シリコンウェーハに対してスリップ転位が発生する可能性がある。このため、スリップ転位の発生を防止するために、シリコンウェーハの熱的強度においても向上させることが有効である。   Further, the heat treatment of the silicon wafer in the techniques described in Patent Documents 1 to 3 is an effective means for eliminating a grown-in defect in the device active region and obtaining a high gettering effect. Therefore, slip dislocation may occur at least with respect to the silicon wafer. For this reason, in order to prevent occurrence of slip dislocation, it is effective to improve the thermal strength of the silicon wafer.

なお、この熱的強度を向上させるには、シリコンウェーハの固溶酸素濃度を高くする技術が周知であるが、固溶酸素濃度が高くなると、前述したように、デバイス活性領域においてもBMDの析出密度が高くなるという問題がある。   In order to improve the thermal strength, a technique for increasing the concentration of dissolved oxygen in the silicon wafer is well known. However, as the concentration of dissolved oxygen increases, as described above, precipitation of BMD also occurs in the device active region. There is a problem that the density becomes high.

本発明は、上述の事情に鑑みてなされたものであり、Grown−in欠陥の無欠陥化や、高いゲッタリング効果を備え、かつ、デバイス活性領域におけるBMDの析出を防止することができ、更に、デバイス活性領域の熱的強度を向上させることができるシリコンウェーハを提供することを目的とする。   The present invention has been made in view of the above-described circumstances, has no defect of grown-in defects, has a high gettering effect, and can prevent precipitation of BMD in the device active region. An object of the present invention is to provide a silicon wafer capable of improving the thermal strength of the device active region.

本発明に係わるシリコンウェーハは、シリコンウェーハの少なくともデバイス活性領域が含まれる無欠陥領域内に固溶酸素濃度が0.7×1018atoms/cm以上の高酸素濃度領域を有し、かつ、前記無欠陥領域内には、格子間シリコンが過飽和状態で含有されていることを特徴とする。 The silicon wafer according to the present invention has a high oxygen concentration region having a solid solution oxygen concentration of 0.7 × 10 18 atoms / cm 3 or more in a defect-free region including at least a device active region of the silicon wafer, and The defect-free region contains interstitial silicon in a supersaturated state.

前記無欠陥領域内の固溶酸素濃度が、前記無欠陥領域よりも深いシリコンウェーハ内部のバルク領域内の固溶酸素濃度よりも高いことが好ましい。   It is preferable that the solid solution oxygen concentration in the defect-free region is higher than the solid solution oxygen concentration in the bulk region inside the silicon wafer deeper than the defect-free region.

前記高酸素濃度領域から前記シリコンウェーハの表面に向かって固溶酸素濃度が漸減していることが好ましい。   It is preferable that the concentration of dissolved oxygen gradually decreases from the high oxygen concentration region toward the surface of the silicon wafer.

本発明は、Grown−in欠陥の無欠陥化や、高いゲッタリング効果を備え、かつ、デバイス活性領域におけるBMDの析出を防止することができ、更に、デバイス活性領域の熱的強度を向上させることができるシリコンウェーハが提供される。   The present invention is capable of eliminating a Grown-in defect, providing a high gettering effect, preventing precipitation of BMD in the device active region, and further improving the thermal strength of the device active region. A silicon wafer is provided.

以下、本発明の実施形態について、図1を参照して説明する。図1は本実施形態に係わるシリコンウェーハを模式的に示した断面図である。なお、本明細書中の固溶酸素濃度は、1970-1979年度版Old ASTM基準の換算係数から求めた値である。   Hereinafter, an embodiment of the present invention will be described with reference to FIG. FIG. 1 is a cross-sectional view schematically showing a silicon wafer according to this embodiment. In addition, the solid solution oxygen concentration in this specification is a value obtained from a conversion factor based on the 1970-1979 edition Old ASTM standard.

本実施形態に係わるシリコンウェーハは、図1に示すように、シリコンウェーハ10の少なくともデバイス活性領域が含まれる無欠陥領域(BMDやGrown−in欠陥(転移クラスタを含む)が存在しない領域:Denuted Zone;以下、DZ層という)12内に、格子間シリコン(Interstitial−Si:図中では「i−Si」という)13が過飽和状態で含有されている。   As shown in FIG. 1, the silicon wafer according to the present embodiment includes a defect-free region (a region in which no BMD or a grown-in defect (including a transfer cluster) exists) including at least a device active region of the silicon wafer 10: ; Hereinafter referred to as a DZ layer) 12 contains interstitial silicon (Interstitial-Si: “i-Si” in the figure) 13 in a supersaturated state.

ここでいう格子間シリコンが過飽和状態で含有されているとは、2段階熱処理(酸素100%雰囲気中で、800℃、4時間の熱処理を行い、更に、同雰囲気(酸素100%)中で、1000℃、16時間熱処理)を行った後に、Satoエッチングを施し、シリコンウェーハ表面を顕微鏡で観察し、表面から深さ5μmまでの領域に存在するエッチピットを測定したときに、前記エッチピット密度が10個/cm以下であることをいう。 The fact that interstitial silicon is contained in a supersaturated state here means a two-stage heat treatment (heat treatment at 800 ° C. for 4 hours in an oxygen 100% atmosphere, and further in the same atmosphere (oxygen 100%) After performing heat treatment at 1000 ° C. for 16 hours, Sato etching is performed, the silicon wafer surface is observed with a microscope, and the etch pit density in the region from the surface to a depth of 5 μm is measured. It means 10 pieces / cm 2 or less.

DZ層12は、ウェーハの表面11からその深さがデバイス活性領域に合わせ同程度あるいはそれよりも深く形成されている。DZ層12の深さは、例えば、5μmである。   The depth of the DZ layer 12 is formed from the surface 11 of the wafer to the same degree or deeper than the device active region. The depth of the DZ layer 12 is, for example, 5 μm.

また、DZ層12には、固溶酸素濃度が0.7×1018atoms/cm以上の高酸素濃度領域を備えている。 The DZ layer 12 includes a high oxygen concentration region having a solid solution oxygen concentration of 0.7 × 10 18 atoms / cm 3 or more.

このように、本発明に係わるシリコンウェーハは、格子間シリコンがDZ層12内に過飽和状態で含有されており、かつ、固溶酸素濃度が0.7×1018atoms/cm以上の高酸素濃度領域を有しているため、Grown−in欠陥の無欠陥化や、高いゲッタリング効果を備え、かつ、デバイス活性領域におけるBMDの析出を防止することができ、更に、デバイス活性領域の熱的強度を向上させることができる。 As described above, the silicon wafer according to the present invention contains interstitial silicon in a supersaturated state in the DZ layer 12 and has a high oxygen concentration of 0.7 × 10 18 atoms / cm 3 or more. Since it has a concentration region, it is possible to eliminate a Grown-in defect, to obtain a high gettering effect, to prevent precipitation of BMD in the device active region, and to further prevent thermal activation of the device active region. Strength can be improved.

なお、格子間シリコンがDZ層12内に過飽和状態で含有されていても、固溶酸素濃度が0.7×1018atoms/cm未満である場合には、シリコンウェーハのデバイス活性領域における熱的強度を向上させることができない。 Even interstitial silicon is contained in a supersaturated state in DZ layer 12, when the solid solution oxygen concentration is less than 0.7 × 10 18 atoms / cm 3, the heat in the device active region of the silicon wafer The mechanical strength cannot be improved.

また、前記固溶酸素濃度が0.7×1018atoms/cm以上であっても、格子間シリコンがDZ層12内に過飽和状態で含有されていない場合には、DZ層12内で固溶酸素がBMD(Balk Micro Defect)として析出されてしまうため好ましくない。 In addition, even if the solid solution oxygen concentration is 0.7 × 10 18 atoms / cm 3 or more, if the interstitial silicon is not contained in the DZ layer 12 in a supersaturated state, the solid solution oxygen is not dissolved in the DZ layer 12. Since dissolved oxygen is deposited as BMD (Balk Micro Defect), it is not preferable.

一方、シリコンウェーハ10のDZ層12よりも深いシリコンウェーハ内部のバルク領域15内には、COP(Crystal Originated Particle)、LSTD(Laser Scattering Tomography Defect)とよばれる過飽和の空孔型点欠陥の凝集体や酸素析出物が残存していても構わない。   On the other hand, in the bulk region 15 inside the silicon wafer deeper than the DZ layer 12 of the silicon wafer 10, an aggregate of supersaturated hole type point defects called COP (Crystal Originating Particle) and LSTD (Laser Scattering Tomography Defect). Or oxygen precipitates may remain.

次に、本発明の実施形態に係わるシリコンウェーハの製造方法について説明する。   Next, the manufacturing method of the silicon wafer concerning embodiment of this invention is demonstrated.

上述した本実施形態に係わるシリコンウェーハを製造するためには、まず、チョクラルスキー法によるシリコン単結晶インゴットの育成時において、固溶酸素濃度が0.7×1018atoms/cm近傍又は0.7×1018atoms/cm以上となるように調整して行う。 To produce a silicon wafer according to the present embodiment described above, first, at the time of growth of a silicon single crystal ingot by the Czochralski method, the solution oxygen concentration is 0.7 × 10 18 atoms / cm 3 or near 0 .7 × 10 18 atoms / cm 3 is adjusted so as to be 3 or more.

具体的には、炉内の石英ルツボに充填した多結晶シリコンを加熱してシリコン融液とし、このシリコン融液の液面上方から種結晶を接触させて、種結晶と石英ルツボを回転させながら引上げ、所望の直径まで拡径して直胴部を育成することでシリコン単結晶インゴットを製造する。この際の前記固溶酸素濃度の調整は、石英ルツボの回転数や炉内圧力などを調整することで行うことができる。   Specifically, the polycrystalline silicon filled in the quartz crucible in the furnace is heated to form a silicon melt, and the seed crystal is brought into contact with the silicon melt from above the liquid surface while rotating the seed crystal and the quartz crucible. A silicon single crystal ingot is manufactured by pulling up and expanding to a desired diameter to grow a straight body portion. The concentration of the dissolved oxygen at this time can be adjusted by adjusting the rotation speed of the quartz crucible or the pressure in the furnace.

次に、製造したシリコン単結晶インゴットを、周知の方法によりシリコンウェーハに加工する。   Next, the manufactured silicon single crystal ingot is processed into a silicon wafer by a known method.

すなわち、前記シリコン単結晶インゴットを内周刃又はワイヤソー等によりウェーハ状にスライスした後、外周部の面取り、ラッピング、エッチング、研磨等の加工工程を経て、シリコンウェーハを製造する。なお、ここで記載された加工工程は例示的なものであり、本発明は、この加工工程のみに限定されるものではない。   That is, after slicing the silicon single crystal ingot into a wafer shape with an inner peripheral blade or a wire saw, a silicon wafer is manufactured through processing steps such as chamfering, lapping, etching, and polishing of the outer peripheral portion. Note that the processing steps described here are exemplary, and the present invention is not limited to this processing step.

次に、前記製造したシリコンウェーハに対して、酸素ガス分圧が20%以上100%以下である酸化性ガス雰囲気中、1300℃以上1380℃以下の温度で、急速加熱・急速冷却熱処理(RTP:Rapid Thermal Process)を行う。   Next, rapid heating / cooling heat treatment (RTP) is performed on the manufactured silicon wafer at a temperature of 1300 ° C. to 1380 ° C. in an oxidizing gas atmosphere having an oxygen gas partial pressure of 20% to 100%. Perform Rapid Thermal Process).

このように、固溶酸素濃度が0.7×1018atoms/cm近傍又は0.7×1018atoms/cm以上のシリコンウェーハに対して、前記条件により急速加熱・急速冷却熱処理を行うことで、前記無欠陥領域内に、格子間シリコンを過飽和状態で含有させることができる。 In this way, a rapid heating / cooling heat treatment is performed on the silicon wafer having a solid solution oxygen concentration in the vicinity of 0.7 × 10 18 atoms / cm 3 or 0.7 × 10 18 atoms / cm 3 or more under the above conditions. Thus, interstitial silicon can be contained in a supersaturated state in the defect-free region.

なお、この急速加熱・急速冷却熱処理は、例えば、図2に示すようなRTP装置を用いて、例えば、図3に示すような温度プロセスにて行う。図2は、本発明のシリコンウェーハの製造に用いられるRTP装置の一例の概要を示す断面図であり、図3は急速加熱・急速冷却熱処理における熱処理プロセスの幾つかの例を示す図である。   The rapid heating / cooling heat treatment is performed by, for example, a temperature process as shown in FIG. 3 using an RTP apparatus as shown in FIG. FIG. 2 is a cross-sectional view showing an outline of an example of an RTP apparatus used for manufacturing a silicon wafer according to the present invention, and FIG.

本発明のシリコンウェーハの製造に用いられるRTP装置10は、図2に示すように、雰囲気ガス導入口20a及び雰囲気ガス排出口20bを備えた反応管20と、反応管20の上部に離間して配置された複数のランプ30と、反応管20内の反応空間25にウェーハWを支持するウェーハ支持部40とを備える。ウェーハ支持部40は、ウェーハWを直接支持する環状のサセプタ40aと、サセプタ40aを支持するステージ40bとを備える。   As shown in FIG. 2, the RTP apparatus 10 used for manufacturing the silicon wafer of the present invention is separated from the reaction tube 20 provided with the atmospheric gas inlet 20a and the atmospheric gas outlet 20b, and at the upper part of the reaction tube 20. A plurality of lamps 30 arranged and a wafer support portion 40 that supports the wafer W in the reaction space 25 in the reaction tube 20 are provided. The wafer support unit 40 includes an annular susceptor 40a that directly supports the wafer W, and a stage 40b that supports the susceptor 40a.

反応管20は、例えば、石英で構成されている。ランプ30は、例えば、ハロゲンランプで構成されている。サセプタ40aは、例えば、シリコンで構成されている。ステージ40bは、例えば、石英で構成されている。   The reaction tube 20 is made of, for example, quartz. The lamp 30 is composed of, for example, a halogen lamp. The susceptor 40a is made of silicon, for example. The stage 40b is made of, for example, quartz.

図2に示すRTP装置10を用いてシリコンウェーハWに対して、急速加熱・急速冷却熱処理(RTP)を行う場合は、反応管20に設けられた図示しないウェーハ導入口より、シリコンウェーハWを反応空間25内に導入し、ウェーハ支持部40のサセプタ40a上にシリコンウェーハWを支持し、その後、雰囲気ガス導入口20aから後述する雰囲気ガスを導入すると共に、ランプ30によりシリコンウェーハW表面に対してランプ照射をすることで行う。なお、このRTP装置10における反応空間25内の温度制御は、ウェーハ支持部40のステージ40bに埋め込まれた複数の放射温度計50によってウェーハWの下部近傍の径方向におけるウェーハ面内の平均温度を測定し、その測定された温度に基づいて複数のハロゲンランプ30の制御(各ランプの個別のON−OFF制御や、発光する光の発光強度の制御等)を行う。   When performing rapid heating / rapid cooling heat treatment (RTP) on the silicon wafer W using the RTP apparatus 10 shown in FIG. 2, the silicon wafer W is reacted from a wafer inlet (not shown) provided in the reaction tube 20. Introduced into the space 25, the silicon wafer W is supported on the susceptor 40a of the wafer support portion 40, and then an atmospheric gas to be described later is introduced from the atmospheric gas inlet 20a. This is done by lamp irradiation. The temperature control in the reaction space 25 in the RTP apparatus 10 is performed by adjusting the average temperature in the wafer surface in the radial direction near the lower portion of the wafer W by a plurality of radiation thermometers 50 embedded in the stage 40b of the wafer support 40. Based on the measured temperature, the plurality of halogen lamps 30 are controlled (individual ON-OFF control of each lamp, emission intensity control of emitted light, etc.).

この急速加熱・急速冷却熱処理における温度プロセスは、例えば、図3(a)に示すように、酸素等の酸化性ガス雰囲気中、10℃/sec以上の速度で最高保持温度Tまで昇温して、最高保持温度Tで所望時間(例えば、1sec〜60sec)保持した後、10℃/sec以上の速度で降温する場合(図3(a))や、はじめにアルゴン等の非酸化性ガス雰囲気において最大保持温度Tまで前記速度で昇温した後、最大保持温度Tで保持中に、酸素ガス等の酸化性ガス雰囲気に切り替えて更に所望時間保持した後、前記速度で降温する場合(図3(b))や、はじめにアルゴン等の非酸化性ガス雰囲気において最大保持温度Tまで昇温し、その後、最大保持温度T(<T)まで一旦降温し、途中、酸素ガス等の酸化性ガス雰囲気中に切り替えた後、再び、最大保持温度T(<T)まで昇温する場合(図3(c))などを用いることができる。 For example, as shown in FIG. 3A, the temperature process in the rapid heating / cooling heat treatment is performed by raising the temperature up to the maximum holding temperature T 1 at a rate of 10 ° C./sec or more in an oxidizing gas atmosphere such as oxygen. Then, after holding at the maximum holding temperature T 1 for a desired time (for example, 1 sec to 60 sec), the temperature is lowered at a rate of 10 ° C./sec or more (FIG. 3A), or first a non-oxidizing gas atmosphere such as argon after raising the temperature at the rate of up to a maximum holding temperature T 1, in a holding at a maximum holding temperature T 1, after holding further desired time it is switched to an oxidizing gas atmosphere such as oxygen gas, if the temperature is decreased by the rate (in FIG. 3 (b)) and the temperature was raised to maximum retention temperature T 2 in a non-oxidizing gas atmosphere such as argon Introduction thereafter once cooled to a maximum holding temperature T 3 (<T 2), the middle, oxygen gas, etc. Oxidation of After switching to a gas atmosphere, again, if the temperature is raised to a maximum holding temperature T 1 (<T 2) (FIG. 3 (c)) or the like can be used.

次に、前記急速加熱・急速冷却熱処理によって、DZ層が形成され、かつ、格子間シリコンが過飽和状態となるメカニズムについて説明する。   Next, the mechanism by which the DZ layer is formed and the interstitial silicon is supersaturated by the rapid heating / cooling heat treatment will be described.

図4は、急速加熱・急速冷却熱処理によって、DZ層が形成され、かつ、格子間シリコンが過飽和状態となるメカニズムについて説明するための概念図である。   FIG. 4 is a conceptual diagram for explaining a mechanism in which the DZ layer is formed and the interstitial silicon is supersaturated by the rapid heating / cooling heat treatment.

前記急速加熱・急速冷却熱処理において酸素分圧が20%以上と酸素濃度が高い状態で急速加熱・急速冷却熱処理による急激な昇温を行うと、シリコンウェーハ表面が酸化されることで、格子間シリコン(i−Si)が生成し、導入される(図4(a))。その後、高温処理中に、シリコン単結晶インゴットの育成時において発生したCOPの内壁に形成された内壁酸化膜に含まれる酸素がシリコンウェーハ内に溶解する。内壁酸化膜が除去されたCOP内に前記生成されたi−Siが埋まることによってCOPが消滅していき(図4(b))、無欠陥領域(DZ層)が形成される(図4(c))。その際、COPが消滅した後、残存する格子間シリコン(i−Si)が、前記無欠陥領域内において格子間シリコンの過飽和状態を形成する(図4(c))。   In the rapid heating / cooling heat treatment, if the oxygen partial pressure is 20% or higher and the oxygen concentration is high, when the rapid heating is performed by the rapid heating / cooling heat treatment, the silicon wafer surface is oxidized, thereby causing interstitial silicon. (I-Si) is generated and introduced (FIG. 4A). Thereafter, during the high temperature treatment, oxygen contained in the inner wall oxide film formed on the inner wall of the COP generated during the growth of the silicon single crystal ingot is dissolved in the silicon wafer. When the generated i-Si is buried in the COP from which the inner wall oxide film has been removed, the COP disappears (FIG. 4B), and a defect-free region (DZ layer) is formed (FIG. 4B). c)). At that time, after the COP disappears, the remaining interstitial silicon (i-Si) forms a supersaturated state of the interstitial silicon in the defect-free region (FIG. 4C).

なお、前記急速加熱・急速冷却熱処理によって、ウェーハの表面近傍にCOPが残存してしまう場合がある。図5は、急速加熱・急速冷却熱処理によって、DZ層が形成され、かつ、格子間シリコンが過飽和状態となるメカニズムにおいて、ウェーハの表面近傍のCOPが残存するメカニズムを説明するための概念図である。   Note that COP may remain near the surface of the wafer due to the rapid heating / cooling heat treatment. FIG. 5 is a conceptual diagram for explaining the mechanism in which the COP in the vicinity of the wafer surface remains in the mechanism in which the DZ layer is formed by the rapid heating / cooling heat treatment and the interstitial silicon is supersaturated. .

なお、前記ウェーハの表面近傍にCOPが残存してしまう場合は、例えば、チョクラルスキー法によるシリコン単結晶インゴットの育成時において、固溶酸素濃度が非常に高い場合(例えば、1.7×1018atoms/cm以上)や、急速加熱・急速冷却熱処理における酸化性雰囲気の酸素分圧が高い場合(例えば、酸素100%雰囲気)等が挙げられる。 In the case where COP remains in the vicinity of the surface of the wafer, for example, when a silicon single crystal ingot is grown by the Czochralski method, the concentration of dissolved oxygen is very high (for example, 1.7 × 10 × 10). 18 atoms / cm 3 or more), or when the oxygen partial pressure of the oxidizing atmosphere in the rapid heating / cooling heat treatment is high (for example, an oxygen 100% atmosphere).

例えば、シリコン単結晶インゴットの育成時における固溶酸素濃度が高かったり、急速加熱・急速冷却熱処理における酸化性雰囲気の酸素分圧が高かったりすると、ウェーハの表面近傍は酸素過飽和の状態となるため、表面近傍に発生しているCOPの内壁に形成された内壁酸化膜に含まれる酸素がウェーハ内に溶解されにくくなる。従って、ウェーハの表面近傍に形成されたCOPの内壁酸化膜は残存してしまう状態となり、この残存した内壁酸化膜がCOP内部にi−Siが埋まるのを妨げてしまうため、表面近傍のCOPを消滅することができない場合がある(図5(a)〜(c))。   For example, if the solid solution oxygen concentration during the growth of a silicon single crystal ingot is high, or if the oxygen partial pressure in the oxidizing atmosphere in the rapid heating / cooling heat treatment is high, the vicinity of the wafer surface is in an oxygen supersaturated state. Oxygen contained in the inner wall oxide film formed on the inner wall of the COP generated near the surface is hardly dissolved in the wafer. Therefore, the COP inner wall oxide film formed near the surface of the wafer remains, and this remaining inner wall oxide film prevents the i-Si from being buried inside the COP. In some cases, it cannot be eliminated (FIGS. 5A to 5C).

この場合には、ウェーハの表面近傍に残存したCOPを研磨により除去することで、格子間シリコンが過飽和状態となった無欠陥領域(DZ層)を形成することができる。なお、この研磨は、一般的に周知技術である仕上げ研磨のみで行ってもよく、周知技術である二次研磨と前記仕上げ研磨とを併用して行ってもよい。   In this case, the defect-free region (DZ layer) in which the interstitial silicon is supersaturated can be formed by removing the COP remaining in the vicinity of the surface of the wafer by polishing. Note that this polishing may be performed only by finish polishing, which is generally a well-known technique, or may be performed in combination with secondary polishing, which is a well-known technique, and the above-described finish polishing.

上述した製造方法により製造された本実施形態に係わるシリコンウェーハ10のウェーハ表面11からその内部方向の固溶酸素濃度の深さ方向分布について図面を参照して説明する。   The depth direction distribution of the dissolved oxygen concentration in the internal direction from the wafer surface 11 of the silicon wafer 10 according to the present embodiment manufactured by the above-described manufacturing method will be described with reference to the drawings.

図6〜図8は、本実施形態に係わるシリコンウェーハの固溶酸素濃度の深さ方向分布を示すグラフである。ここで、図6〜図8の横軸は、シリコンウェーハ表面からの深さ(μm)であり、縦軸は固溶酸素濃度(×1018atoms/cm)である。なお、図6は、前述した図4に示すような場合において、格子間シリコンが過飽和状態となったときの固溶酸素濃度の深さ方向分布であり、図7は、前述した図5に示すような場合において、格子間シリコンが過飽和状態となったときの表面のCOPを研磨した場合における固溶酸素濃度の深さ方向分布であり、図8は、図7よりもその研磨量が更に多い場合の固溶酸素濃度の深さ方向分布である。 6 to 8 are graphs showing the distribution in the depth direction of the dissolved oxygen concentration of the silicon wafer according to the present embodiment. Here, the horizontal axis of FIGS. 6 to 8 is the depth (μm) from the surface of the silicon wafer, and the vertical axis is the solid solution oxygen concentration (× 10 18 atoms / cm 3 ). 6 shows the depth direction distribution of the dissolved oxygen concentration when the interstitial silicon is supersaturated in the case shown in FIG. 4, and FIG. 7 shows the above-described FIG. FIG. 8 shows the depth direction distribution of the dissolved oxygen concentration when the surface COP is polished when the interstitial silicon is supersaturated in such a case. FIG. 8 shows a larger amount of polishing than FIG. It is a depth direction distribution of the solid solution oxygen concentration in the case.

本実施形態に係わるシリコンウェーハの固溶酸素濃度の深さ方向分布は、シリコンウェーハの少なくともデバイス活性領域が含まれる無欠陥領域(例えば、ウェーハ表面からの深さが5μm以内の領域)内に固溶酸素濃度が0.7×1018atoms/cm以上の最大値を有する高酸素濃度領域を有し、かつ、前記無欠陥領域よりも深いシリコンウェーハ内部のバルク領域(例えば、ウェーハ表面からの深さが5μmを超える領域)においても固溶酸素濃度が0.7×1018atoms/cm以上である場合(図6(2)〜(3)、図7(6)〜(7):以下、第1の形態という)、前記第1の形態に変えて、前記バルク領域においては、固溶酸素濃度が0.7×1018atoms/cm未満である場合(図6(1)、図7(5):以下、第2の形態という)及び、固溶酸素濃度が0.7×1018atoms/cm以上のピーク値(最大値)を有さないが、前記無欠陥領域及び前記バルク領域において固溶酸素濃度が0.7×1018atoms/cm以上である場合(図6(4)、図7(8)、図8(9)〜(11))である。 In the depth direction distribution of the dissolved oxygen concentration of the silicon wafer according to this embodiment, the solid-state oxygen concentration of the silicon wafer is fixed within a defect-free region (for example, a region having a depth of 5 μm or less from the wafer surface) including at least the device active region. A high oxygen concentration region having a maximum dissolved oxygen concentration of 0.7 × 10 18 atoms / cm 3 or more and a deep region inside the silicon wafer deeper than the defect-free region (for example, from the wafer surface) Even in the case where the depth exceeds 5 μm, the solid solution oxygen concentration is 0.7 × 10 18 atoms / cm 3 or more (FIGS. 6 (2) to (3) and FIGS. 7 (6) to (7): (Hereinafter referred to as the first form), instead of the first form, in the bulk region, the solid solution oxygen concentration is less than 0.7 × 10 18 atoms / cm 3 (FIG. 6 (1), FIG. 5): hereinafter referred to as the second embodiment) and the solid solution oxygen concentration does not have a peak value (maximum value) of 0.7 × 10 18 atoms / cm 3 or more, but the defect-free region and the bulk region In FIG. 6, the solid solution oxygen concentration is 0.7 × 10 18 atoms / cm 3 or more (FIG. 6 (4), FIG. 7 (8), and FIGS. 8 (9) to (11)).

この中で、無欠陥領域内の固溶酸素濃度が、前記無欠陥領域よりも深いシリコンウェーハ内部のバルク領域内の固溶酸素濃度よりも高い実施形態(図6(1)〜(3)、図7(5)〜(7))を備えていることが好ましい。   Among these, an embodiment in which the solid solution oxygen concentration in the defect-free region is higher than the solid solution oxygen concentration in the bulk region inside the silicon wafer deeper than the defect-free region (FIGS. 6 (1) to (3), 7 (5) to (7) are preferably provided.

このような構成を備えることで、前記バルク領域に生じたBMDあるいは裏面から生じたスリップ転位等を前記バルク領域内でピンニングすることができ、ウェーハ表面のデバイス形成領域への伝播を防止することができる。   By providing such a configuration, BMD generated in the bulk region or slip dislocation generated from the back surface can be pinned in the bulk region, and propagation to the device formation region on the wafer surface can be prevented. it can.

更に、前記高酸素濃度領域から前記シリコンウェーハの表面に向かって前記固溶酸素濃度が漸減している実施形態(図6(1)〜(4)、図7(8))を備えていることがより好ましい。   Furthermore, the embodiment (FIGS. 6 (1) to (4) and FIG. 7 (8)) in which the dissolved oxygen concentration gradually decreases from the high oxygen concentration region toward the surface of the silicon wafer is provided. Is more preferable.

このような構成を備えることで、表面に形成されるサーマルドナーの生成量を抑制することができる。   By providing such a configuration, the generation amount of thermal donors formed on the surface can be suppressed.

次に、幾つかの実施例により本発明の効果について具体的に説明するが、本発明は下記の実施例に限定されるものではない。   Next, the effects of the present invention will be specifically described with reference to some examples, but the present invention is not limited to the following examples.

(実施例1〜9)
CZ法によるシリコン単結晶インゴット作製時において、固溶酸素濃度を0.5、0.7、1.2、1.7(×1018atoms/cm)(1970-1979年度版Old ASTMによる換算係数からの算出値)で各々調整して、V/G(引上速度Vと、1300℃における結晶軸方向の温度勾配G)を制御しながら、空孔型点欠陥の凝集体が存在する空孔型点欠陥領域(I領域)が全面に形成されるように引き上げを行い、[Oi]が異なるP型、結晶面方位(001)である3種類のシリコン単結晶インゴットを作製した。
(Examples 1-9)
When producing a silicon single crystal ingot by the CZ method, the solid solution oxygen concentration is 0.5, 0.7, 1.2, 1.7 (× 10 18 atoms / cm 3 ) (converted by 1970-1979 version Old ASTM) The vacancy in which vacancy-type point defect aggregates exist while controlling V / G (the pulling speed V and the temperature gradient G in the crystal axis direction at 1300 ° C.) by adjusting each with the calculated value from the coefficient. Pulling was performed so that a hole-type point defect region (I region) was formed on the entire surface, and three types of silicon single crystal ingots having P-type and crystal plane orientation (001) with different [Oi] were produced.

次に、得られたシリコン単結晶インゴットを、ワイヤソーによりウェーハ状に切断し、ベベル加工、ラッピング、エッチング、研磨を施して、両面研磨された直径が300mmのシリコンウェーハを作製した。   Next, the obtained silicon single crystal ingot was cut into a wafer shape with a wire saw and subjected to bevel processing, lapping, etching, and polishing, and a double-side polished silicon wafer having a diameter of 300 mm was produced.

次に、図2に示すようなRTP装置10を用いて、図3(a)に示すような温度プロセスにて、100%の酸素雰囲気下で、昇温速度75℃/sec、最高到達温度1300℃、最高到達温度における保持時間を30sec、降温速度25℃/secの条件下で急速加熱・急速冷却熱処理を行い、図6(1)に示すような固溶酸素濃度分布を有するシリコンウェーハ(実施例1:固溶酸素濃度0.5×1018atoms/cm)、図6(2)に示すような固溶酸素濃度分布を有するシリコンウェーハ(実施例2:固溶酸素濃度0.7×1018atoms/cm)、図6(3)に示すような固溶酸素濃度分布を有するシリコンウェーハ(実施例3:固溶酸素濃度1.2×1018atoms/cm)、図6(4)に示すような固溶酸素濃度分布を有するシリコンウェーハ(実施例4:固溶酸素濃度1.7×1018atoms/cm)を各々作製した。 Next, using the RTP apparatus 10 as shown in FIG. 2, in the temperature process as shown in FIG. 3A, the temperature rising rate is 75 ° C./sec and the maximum temperature reached 1300 in a 100% oxygen atmosphere. A silicon wafer having a solid solution oxygen concentration distribution as shown in FIG. 6 (1) is performed by performing rapid heating / cooling heat treatment under the conditions of 30 ° C., a holding time at the maximum temperature of 30 seconds, and a temperature drop rate of 25 ° C./sec. Example 1: Solid solution oxygen concentration 0.5 × 10 18 atoms / cm 3 ), silicon wafer having solid solution oxygen concentration distribution as shown in FIG. 6 (2) (Example 2: solid solution oxygen concentration 0.7 × 10 18 atoms / cm 3 ), a silicon wafer having a solid solution oxygen concentration distribution as shown in FIG. 6 (3) (Example 3: solid solution oxygen concentration 1.2 × 10 18 atoms / cm 3 ), FIG. 4) As shown Silicon wafers with溶酸oxygen concentration distribution: to produce respectively (Example 4 dissolved oxygen concentration 1.7 × 10 18 atoms / cm 3 ).

また、急速加熱・急速冷却熱処理を行った実施例1〜4と同ロット(同固溶酸素濃度)のサンプルについて表面から取代2.5μm程度の表面研磨を行い、図7(5)に示すような固溶酸素濃度分布を有するシリコンウェーハ(実施例5:固溶酸素濃度0.5×1018atoms/cm)、図7(6)に示すような固溶酸素濃度分布を有するシリコンウェーハ(実施例6:固溶酸素濃度0.7×1018atoms/cm)、図7(7)に示すような固溶酸素濃度分布を有するシリコンウェーハ(実施例7:固溶酸素濃度1.2×1018atoms/cm)、図7(8)に示すような固溶酸素濃度分布を有するシリコンウェーハ(実施例8:固溶酸素濃度1.7×1018atoms/cm)を各々作製した。 Further, the sample of the same lot (same dissolved oxygen concentration) as in Examples 1 to 4 subjected to the rapid heating / cooling heat treatment was subjected to surface polishing of about 2.5 μm from the surface, as shown in FIG. Silicon wafer having a solid solution oxygen concentration distribution (Example 5: solid solution oxygen concentration 0.5 × 10 18 atoms / cm 3 ), a silicon wafer having a solid solution oxygen concentration distribution as shown in FIG. Example 6: A silicon wafer having a solid solution oxygen concentration distribution as shown in FIG. 7 (7) (Example 7: solid solution oxygen concentration 1.2), with a solid solution oxygen concentration 0.7 × 10 18 atoms / cm 3 ). × 10 18 atoms / cm 3 ) and silicon wafers having a solid solution oxygen concentration distribution as shown in FIG. 7 (8) (Example 8: solid solution oxygen concentration 1.7 × 10 18 atoms / cm 3 ) were produced. did.

また、急速加熱・急速冷却熱処理を行った実施例2〜4と同ロット(同固溶酸素濃度)のサンプルについて表面から取代5.0μm程度の表面研磨を行い、図8(9)に示すような固溶酸素濃度分布を有するシリコンウェーハ(実施例9:固溶酸素濃度0.7×1018atoms/cm)、図8(10)に示すような固溶酸素濃度分布を有するシリコンウェーハ(実施例10:固溶酸素濃度1.2×1018atoms/cm)、図8(11)に示すような固溶酸素濃度分布を有するシリコンウェーハ(実施例11:固溶酸素濃度1.7×1018atoms/cm)を各々作製した。 Further, the samples of the same lot (same dissolved oxygen concentration) as those of Examples 2 to 4 subjected to the rapid heating / cooling heat treatment were subjected to surface polishing of about 5.0 μm from the surface, as shown in FIG. 8 (9). Silicon wafer having a solid solution oxygen concentration distribution (Example 9: solid solution oxygen concentration 0.7 × 10 18 atoms / cm 3 ), a silicon wafer having a solid solution oxygen concentration distribution as shown in FIG. Example 10: a silicon wafer having a solid solution oxygen concentration distribution as shown in FIG. 8 (11) (Example 11: solid solution oxygen concentration 1.7), with a solid solution oxygen concentration of 1.2 × 10 18 atoms / cm 3 ). × 10 18 atoms / cm 3 ) were produced.

(比較例1〜2)
CZ法によるシリコン単結晶インゴット作製時において、固溶酸素濃度を0.3、0.5(×1018atoms/cm)に調整して、その他は、実施例9から11と同様な方法(急速加熱・急速冷却熱処理+取代5.0μm程度の表面研磨)で、図9(12)に示すような固溶酸素濃度分布を有するシリコンウェーハ(比較例1:固溶酸素濃度0.3×1018atoms/cm)及び図9(13)に示すような固溶酸素濃度分布を有するシリコンウェーハ(比較例2:固溶酸素濃度0.5×1018atoms/cm)を作製した。
(Comparative Examples 1-2)
At the time of producing the silicon single crystal ingot by the CZ method, the solid solution oxygen concentration was adjusted to 0.3, 0.5 (× 10 18 atoms / cm 3 ), and other methods similar to those in Examples 9 to 11 ( A silicon wafer having a solid solution oxygen concentration distribution as shown in FIG. 9 (12) by rapid heating / cooling heat treatment + surface polishing of about 5.0 μm of machining allowance (Comparative Example 1: solid solution oxygen concentration 0.3 × 10) 18 atoms / cm 3 ) and a silicon wafer having a solid solution oxygen concentration distribution as shown in FIG. 9 (13) (Comparative Example 2: solid solution oxygen concentration 0.5 × 10 18 atoms / cm 3 ) were produced.

(比較例3〜5)
CZ法によるシリコン単結晶インゴット作製時において、固溶酸素濃度を0.7、1.2、1.7(×1018atoms/cm)(1970-1979年度版Old ASTMによる換算係数からの算出値)で各々調整して、かつ、V/G(引上速度Vと、1300℃における結晶軸方向の温度勾配G)を制御しながら、空孔型点欠陥の凝集体が存在せず、格子間シリコン型点欠陥リッチな無欠陥領域が全面に形成されるように、引き上げを行い、固溶酸素濃度が異なるP型、結晶面方位(001)である複数のシリコン単結晶インゴットを作製した。
(Comparative Examples 3-5)
At the time of producing a silicon single crystal ingot by the CZ method, the solid solution oxygen concentration is 0.7, 1.2, 1.7 (× 10 18 atoms / cm 3 ) (calculated from the conversion factor by the 1970-1979 version Old ASTM). Value) and controlling V / G (pulling speed V and temperature gradient G in the crystal axis direction at 1300 ° C.), there is no agglomeration of vacancy-type point defects, and the lattice A plurality of silicon single crystal ingots having P-type and crystal plane orientations (001) having different solid solution oxygen concentrations were produced so that a defect-free region rich in interstitial silicon type point defects was formed on the entire surface.

得られたシリコン単結晶インゴットを、ワイヤソーによりウェーハ状に切断し、ベベル加工、ラッピング、エッチング、研磨を施して、両面研磨された直径が300mmのシリコンウェーハを作製し、図9(14)に示すような固溶酸素濃度分布を有するシリコンウェーハ(比較例3:固溶酸素濃度0.7×1018atoms/cm)、図9(15)に示すような固溶酸素濃度分布を有するシリコンウェーハ(比較例4:固溶酸素濃度1.2×1018atoms/cm)、図9(16)に示すような固溶酸素濃度分布を有するシリコンウェーハ(比較例5:固溶酸素濃度1.7×1018atoms/cm)を各々作製した。 The obtained silicon single crystal ingot was cut into a wafer shape with a wire saw and subjected to bevel processing, lapping, etching, and polishing to produce a silicon wafer having a diameter of 300 mm that was polished on both sides, as shown in FIG. 9 (14). A silicon wafer having such a dissolved oxygen concentration distribution (Comparative Example 3: dissolved oxygen concentration 0.7 × 10 18 atoms / cm 3 ), a silicon wafer having a dissolved oxygen concentration distribution as shown in FIG. (Comparative example 4: solid solution oxygen concentration 1.2 × 10 18 atoms / cm 3 ), a silicon wafer having a solid solution oxygen concentration distribution as shown in FIG. 9 (16) (comparative example 5: solid solution oxygen concentration 1. each was prepared 7 × 10 18 atoms / cm 3 ).

(酸素析出物密度の評価)
実施例1から11及び比較例1から5の各々のサンプルに対して酸素100%雰囲気下で、800℃、4時間の熱処理を行い、その後、同一の雰囲気(酸素100%)下で、1000℃、16時間熱処理を行った後に、Satoエッチング(液組成;HF(濃度49%):HNO3(濃度69%):CHCOOH:HO=1:15:3:1)を施し、サンプル表面を顕微鏡で表面を観察し、表面から深さ5μmまでの領域に存在するエッチピットの密度を計測した。
(Evaluation of oxygen precipitate density)
Each sample of Examples 1 to 11 and Comparative Examples 1 to 5 was subjected to a heat treatment at 800 ° C. for 4 hours in an oxygen 100% atmosphere, and then 1000 ° C. in the same atmosphere (oxygen 100%). , after the 16 hours heat treatment, Sato etching (liquid composition; HF (concentration 49%): HNO3 (69% concentration): CH 3 COOH: H 2 O = 1: 15: 3: 1) to subjecting the sample surface The surface was observed with a microscope, and the density of etch pits existing in the region from the surface to a depth of 5 μm was measured.

その結果、実施例1から11と比較例1および2のサンプルでは、エッチピット密度が10個/cm2以下であり、ほとんどエッチピットは観察されなかったが、比較例3から5のサンプルでは、酸素析出物密度が10個/cm2を超えており多くのエッチピットが確認された。 As a result, in the samples of Examples 1 to 11 and Comparative Examples 1 and 2, the etch pit density was 10 pieces / cm 2 or less, and almost no etch pits were observed, but in the samples of Comparative Examples 3 to 5, The density of oxygen precipitates exceeded 10 pieces / cm 2 , and many etch pits were confirmed.

(スリップの評価)
実施例1から11及び比較例1から5の各々のサンプルに対して、前述した酸素析出物密度の評価よりも過酷な条件(酸素100%雰囲気下で、1200℃、1時間の熱処理)を行い、各々のサンプルのデバイス形成面となる無欠陥領域におけるスリップ転位の発生状況を評価した。
(Slip evaluation)
Each sample of Examples 1 to 11 and Comparative Examples 1 to 5 was subjected to conditions more severe than the above-described evaluation of oxygen precipitate density (heat treatment at 1200 ° C. for 1 hour in an oxygen 100% atmosphere). The occurrence of slip dislocations in the defect-free region serving as the device formation surface of each sample was evaluated.

その結果、比較例1および2のサンプルについては、ウェーハ表面のデバイス形成領域に裏面からスリップが伝播していることが確認されたが、他のサンプルについては、裏面からスリップが表面のデバイス活性領域に到達しているものは確認されなかった。   As a result, for the samples of Comparative Examples 1 and 2, it was confirmed that the slip propagated from the back surface to the device formation region on the wafer surface. Nothing was reached that reached.

本実施形態に係わるシリコンウェーハを模式的に示した断面図である。It is sectional drawing which showed typically the silicon wafer concerning this embodiment. 本実施形態に係わるシリコンウェーハの固溶酸素濃度の深さ方向分布を示すグラフである。It is a graph which shows the depth direction distribution of the solid solution oxygen concentration of the silicon wafer concerning this embodiment. 急速加熱・急速冷却熱処理における温度プロセスの一例を概念図である。It is a conceptual diagram of an example of the temperature process in rapid heating and rapid cooling heat processing. 急速加熱・急速冷却熱処理によって、DZ層が形成され、かつ、格子間シリコンが過飽和状態となるメカニズムについて説明するための概念図である。It is a conceptual diagram for demonstrating the mechanism in which a DZ layer is formed and the interstitial silicon will be in a supersaturated state by rapid heating / rapid cooling heat treatment. 急速加熱・急速冷却熱処理によって、DZ層が形成され、かつ、格子間シリコンが過飽和状態となるメカニズムにおいて、ウェーハの表面近傍のCOPが残存するメカニズムを説明するための概念図である。It is a conceptual diagram for demonstrating the mechanism in which the COP near the surface of the wafer remains in the mechanism in which the DZ layer is formed by the rapid heating / cooling thermal process and the interstitial silicon is supersaturated. 本実施形態に係わるシリコンウェーハの固溶酸素濃度の深さ方向分布を示すグラフである。It is a graph which shows the depth direction distribution of the solid solution oxygen concentration of the silicon wafer concerning this embodiment. 本実施形態に係わるシリコンウェーハの固溶酸素濃度の深さ方向分布を示すグラフである。It is a graph which shows the depth direction distribution of the solid solution oxygen concentration of the silicon wafer concerning this embodiment. 本実施形態に係わるシリコンウェーハの固溶酸素濃度の深さ方向分布を示すグラフである。It is a graph which shows the depth direction distribution of the solid solution oxygen concentration of the silicon wafer concerning this embodiment. 比較例に係わるシリコンウェーハの固溶酸素濃度の深さ方向分布を示すグラフである。It is a graph which shows the depth direction distribution of the solid solution oxygen concentration of the silicon wafer concerning a comparative example.

符号の説明Explanation of symbols

10 シリコンウェーハ
12 DZ層
13 固溶酸素
14 格子間シリコン
15 バルク領域
10 Silicon wafer 12 DZ layer 13 Solid solution oxygen 14 Interstitial silicon 15 Bulk region

Claims (3)

シリコンウェーハの少なくともデバイス活性領域が含まれる無欠陥領域内に固溶酸素濃度が0.7×1018atoms/cm以上の高酸素濃度領域を有し、かつ、前記無欠陥領域内には、格子間シリコンが過飽和状態で含有されていることを特徴とするシリコンウェーハ。 A silicon wafer has a high oxygen concentration region having a solid solution oxygen concentration of 0.7 × 10 18 atoms / cm 3 or more in a defect-free region including at least a device active region, and in the defect-free region, A silicon wafer containing interstitial silicon in a supersaturated state. 前記無欠陥領域内の固溶酸素濃度が、前記無欠陥領域よりも深いシリコンウェーハ内部のバルク領域内の固溶酸素濃度よりも高いことを特徴とする請求項1に記載のシリコンウェーハ。   2. The silicon wafer according to claim 1, wherein a solid solution oxygen concentration in the defect-free region is higher than a solid solution oxygen concentration in a bulk region inside the silicon wafer deeper than the defect-free region. 前記高酸素濃度領域から前記シリコンウェーハの表面に向かって固溶酸素濃度が漸減していることを特徴とする請求項1又は2に記載のシリコンウェーハ。


3. The silicon wafer according to claim 1, wherein a solid solution oxygen concentration gradually decreases from the high oxygen concentration region toward a surface of the silicon wafer.


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