JP2008292351A - Dopant profile measuring thin piece sample preparing method - Google Patents
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- 239000002019 doping agent Substances 0.000 title claims abstract description 35
- 238000000034 method Methods 0.000 title claims description 9
- 238000010884 ion-beam technique Methods 0.000 claims abstract description 54
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims abstract description 30
- 229910052733 gallium Inorganic materials 0.000 claims abstract description 30
- 239000007789 gas Substances 0.000 claims abstract description 28
- 239000004065 semiconductor Substances 0.000 claims abstract description 13
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229910001882 dioxygen Inorganic materials 0.000 claims abstract description 7
- 239000010409 thin film Substances 0.000 claims description 8
- 238000005520 cutting process Methods 0.000 claims description 4
- 238000005464 sample preparation method Methods 0.000 claims 1
- 238000005259 measurement Methods 0.000 abstract description 20
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 abstract description 12
- 238000001093 holography Methods 0.000 abstract description 12
- 238000010894 electron beam technology Methods 0.000 abstract description 10
- 229910052786 argon Inorganic materials 0.000 abstract description 6
- 238000004544 sputter deposition Methods 0.000 abstract description 6
- 239000000523 sample Substances 0.000 description 20
- 150000002500 ions Chemical class 0.000 description 14
- 239000010408 film Substances 0.000 description 10
- 230000001133 acceleration Effects 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- 230000002950 deficient Effects 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 239000006061 abrasive grain Substances 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 239000008119 colloidal silica Substances 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 229910003460 diamond Inorganic materials 0.000 description 2
- 239000010432 diamond Substances 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 238000005498 polishing Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 1
- 238000005430 electron energy loss spectroscopy Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002513 implantation Methods 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052756 noble gas Inorganic materials 0.000 description 1
- 238000007781 pre-processing Methods 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
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Abstract
Description
本発明は、半導体デバイスのドーパントプロファイル測定用の薄片試料作成に関するものである。 The present invention relates to the preparation of a flake sample for measuring a dopant profile of a semiconductor device.
走査キャパシタンス顕微鏡(SCM)で金属探針直下の微少領域の容量変化を測定することによりMOS構造のドーパントのプロファイル測定が行われている(非特許文献1)。走査キャパシタンス顕微鏡測定ではドーパントの分布のみならずスパイク欠陥なども検出可能である。電子線ホログラフィーを用いてpn接合を含む断面の位相像から電位分布像に変換することでドーパントプロファイル測定が行われている(非特許文献2)。 The profile measurement of the dopant of the MOS structure is performed by measuring the capacitance change in a very small region immediately below the metal probe with a scanning capacitance microscope (SCM) (Non-patent Document 1). The scanning capacitance microscope measurement can detect not only the dopant distribution but also spike defects. Dopant profile measurement is performed by converting a phase image of a cross section including a pn junction into a potential distribution image using electron beam holography (Non-patent Document 2).
従来の走査キャパシタンス顕微鏡用のサンプル作製ではワイヤーソウなどで不良箇所やドーパントプロファイル測定したい個所を含む領域を切り出し、ダイヤモンド砥粒またはコロイダルシリカを用いた精密研磨で薄くしていく方法をとっていた。集束イオンビーム装置(FIB)で不良箇所やドーパントプロファイル測定したい個所を含む領域を切り出した場合にもガリウム注入領域の除去にダイヤモンド砥粒またはコロイダルシリカを用いた精密研磨を用いていた。そのため不良箇所やドーパントプロファイル測定したい個所をピンポイントで切り出すのは困難であった。ここで、ピンポイントで切り出すとは、狙った位置が含まれかつ削りだしが少なくて済むようにできるだけ少ないサンプル量で切り出すという意味である。また走査キャパシタンス顕微鏡測定には、探針と測定領域のシリコンの間に適度な酸化膜が必要で、この酸化膜の作成は、測定領域のシリコンを300℃に加熱した状態で、該領域に20分程度紫外線光を照射して行っていた。 In the preparation of a sample for a conventional scanning capacitance microscope, a method including cutting a region including a defective portion or a portion where a dopant profile is desired to be measured with a wire saw, and thinning by precision polishing using diamond abrasive grains or colloidal silica is employed. Even when a region including a defective portion or a portion where a dopant profile is desired to be measured is cut out by a focused ion beam apparatus (FIB), precision polishing using diamond abrasive grains or colloidal silica is used to remove the gallium implantation region. Therefore, it is difficult to pinpoint a defective portion or a portion where a dopant profile is desired to be measured. Here, cutting out at a pinpoint means cutting out with a sample amount as small as possible so that the target position is included and less shaving is required. In addition, the scanning capacitance microscope measurement requires an appropriate oxide film between the probe and the silicon in the measurement region. This oxide film is formed in a state where the silicon in the measurement region is heated to 300 ° C. It was performed by irradiating ultraviolet light for about minutes.
故障箇所を集束イオンビーム装置によりピンポイントで切り出し、該切り出した部分を透過型電子顕微鏡(TEM)で評価を行う事が行われている(非特許文献3)。透過型電子顕微鏡の評価においては、構造的な問題や、電子エネルギー損失分光(EELS)分析により組成は分るが、ドーパント分布などの電気的な物性を知ることができなかった。集束イオンビーム装置によりピンポイントで切り出したデバイス断面において、設計どおりのドーパント分布になっているか測定する方法や、集束イオンビームでピンポイントで切り出した故障箇所の電気的な特性を調べる方法が求められている(特許文献1)。 It has been practiced to cut out a failed portion at a pinpoint with a focused ion beam apparatus and evaluate the cut-out portion with a transmission electron microscope (TEM) (Non-patent Document 3). In the evaluation of a transmission electron microscope, the composition was found by structural problems and electron energy loss spectroscopy (EELS) analysis, but electrical properties such as dopant distribution could not be known. There is a need for a method for measuring whether the dopant distribution is designed as designed in the cross-section of the device cut out with a focused ion beam device, and a method for examining the electrical characteristics of the failure point cut out with a focused ion beam. (Patent Document 1).
上記要望を実現し信頼性のある走査キャパシタンス顕微鏡測定を行うためには、測定領域のシリコン表面に適度な酸化膜の形成に加え、集束イオンビームによる切り出しに伴う、切り出し部分に注入されたガリウムや切り出し部分に形成されたダメージ層の除去が必要になる。また凹凸も容量に影響するので少なくしなければならなかった。又、電子線ホログラフィーを用いたドーパントプロファイル測定を行うには注入ガリウムを除去し、電子線が透過できるように凹凸の少ないまま試料を薄くしなければならない。信頼性高いデータを得るためには薄くした試料のダメージ領域を低減しなければならない。
本発明は、半導体デバイスの所望の断面のドーパントプロファイル測定、もしくは電子線ホログラフィーによるドーパントプロファイル測定を可能にすることを目的とする。 An object of the present invention is to enable measurement of a dopant profile of a desired cross section of a semiconductor device or measurement of a dopant profile by electron holography.
上記課題を解決するために、本発明においては、半導体デバイスから、集束イオンビーム装置で薄片試料を切り出し、該切り出した薄片試料の断面の薄膜化や注入ガリウムの除去に、ガスクラスターイオンビームを用いて、切り出した断面の狭い領域に、低ダメージで凹凸の少ない除去加工を施す。ガスクラスターイオンビーム装置を用いれば、そのクラスターサイズと1原子あたりの入射エネルギーの組み合わせを最適化することにより、狭い領域に低ダメージで凹凸の少ない除去加工ができる。 In order to solve the above-described problems, in the present invention, a gas sample ion beam is used to cut a thin sample from a semiconductor device with a focused ion beam apparatus, and to reduce the cross-section of the cut thin sample and to remove implanted gallium. Then, removal processing with less damage and less unevenness is applied to the narrow region of the cut-out cross section. If a gas cluster ion beam device is used, the combination of the cluster size and the incident energy per atom can be optimized, so that removal processing with less damage and less unevenness can be performed in a narrow area.
また酸素ガスクラスターイオンビームを用いれば、そのクラスターサイズや1原子あたりの入射エネルギーを制御することにより、ストイキオメトリーが良く、すなわち形成した酸化膜の化学組成がよりSi02に近く、膜厚制御性の良いシリコン酸化膜が得られる。再現性の良い薄い酸化膜が得られれば、走査キャパシタンス顕微鏡で、信頼性の良いドーパントプロファイルデータを得ることができる。 Also the use of the oxygen gas cluster ion beam, its by controlling the cluster size and the incident energy per atom, good stoichiometry, i.e. chemical composition closer to Si0 2 of the formed oxide film thickness control A good silicon oxide film can be obtained. If a thin oxide film with good reproducibility is obtained, reliable dopant profile data can be obtained with a scanning capacitance microscope.
デバイス断面を、電子線ホログラフィーを用いてドーパントプロファイル測定を行う場合は、100〜200kVの電子線が透過する厚さまで、集束イオンビーム装置で半導体デバイスから切り出した薄片の断面を、ガスクラスターイオンビームのスパッタで薄くする。 When the dopant profile is measured using electron holography for the device cross-section, the cross-section of the slice cut from the semiconductor device with a focused ion beam device is cut into the thickness of the electron beam of 100 to 200 kV. Thin by sputtering.
クラスターイオンビームは原子1個あたりのエネルギーが低く、サンプルに深く注入されることはない。希ガスのクラスターイオンを用いれば、もしイオンが注入されても不活性であるためガリウムのようにドーパントプロファイル測定に影響を与えることはない。クラスターイオンビームのラテラルスパッタ効果(ガスクラスターイオンビームには平面から突き出たところがスパッタされやすい(平坦化しやすい)効果があり、これをラテラルスパッタ効果と呼ぶ)で凹凸の少ない除去断面が得られる。 The cluster ion beam has a low energy per atom and is not implanted deep into the sample. If noble gas cluster ions are used, the dopant profile measurement is not affected unlike gallium because it is inactive even if ions are implanted. The cluster ion beam has a lateral sputtering effect (the gas cluster ion beam has an effect of being easily sputtered (prone to flatten) when protruding from the plane, which is referred to as a lateral sputtering effect), and a removal cross section with less unevenness can be obtained.
酸素ガスクラスターイオンビームで条件を最適化することにより、ストイキオメトリーが良くて適度に薄い酸化膜を再現性良く形成することができる。この場合も酸素ガスクラスターイオンビームで凹凸の少ない酸化膜表面が得られる。 By optimizing the conditions with an oxygen gas cluster ion beam, an oxide film with good stoichiometry and a moderately thin thickness can be formed with good reproducibility. In this case as well, an oxide film surface with less unevenness can be obtained with an oxygen gas cluster ion beam.
以下に本発明の実施例について図面を用いて詳細に説明する。 Embodiments of the present invention will be described below in detail with reference to the drawings.
図1は、集束イオンビーム装置で半導体デバイスから切り出した薄片6の断面を、ガスクラスターイオンビームを用いてエッチングして、電子線ホログラフィーのためのドーパントプロファイル測定用サンプルを作製する場合を説明するための、薄片6の処理工程毎の概略断面図(薄片6の測定断面に垂直で、かつ、半導体デバイス表面に平行な方向から切断した場合の断面図)である。
FIG. 1 illustrates a case where a cross section of a
集束イオンビームを照射して、半導体デバイスの所望の位置で断面を形成し、該断面を含む薄片6を集束イオンビーム装置から取り出す。薄片6には、集束イオンビームが照射された時に、ガリウムが注入され残留ガリウム層3が存在する。取り出した薄片6を、走査キャパシタンス顕微鏡や電子線ホログラフィーでドーパントプロファイル測定可能にするのに必要な前処理を行うために、ガスクラスターイオンビーム装置に導入する。ガスクラスターイオンビーム装置に複合した光学顕微鏡または走査電子顕微鏡で観察しながら、薄片6の表面の残留ガリウム層3がガスクラスターイオンビームの照射位置にくるように位置を調整する。
The focused ion beam is irradiated to form a cross section at a desired position of the semiconductor device, and the
クラスターサイズと1原子あたりの入射エネルギーの組み合わせを最適化したイオンドーズ量1014ions/cm2〜1016ions/cm2、加速電圧10〜20kVのアルゴン等の希ガスのガスクラスターイオンビーム1を薄片6に照射し(図1(a))、集束イオンビーム装置で切り出した薄片6の表面に注入された30nm程度の残留ガリウム層3が除去できるまで表面のスパッタを行う(図1(b))。電子線ホログラフィーを用いてドーパントプロファイル測定する場合は、薄片6をひっくり返して裏面に注入された30nm程度の残留ガリウム層3の除去も行う(図1(c))。サンプルをひっくり返したのち再びガスクラスターイオンビーム装置に複合した光学顕微鏡または走査電子顕微鏡で観察しながら、残留ガリウム除去後の薄片2の表面がガスクラスターイオンビームの照射位置にくるように位置を調整する。
A gas cluster ion beam 1 of a rare gas such as argon with an ion dose of 10 14 ions / cm 2 to 10 16 ions / cm 2 and an acceleration voltage of 10 to 20 kV optimized for the combination of cluster size and incident energy per atom. The
電子線ホログラフィーを用いてドーパントプロファイルを測定する場合は、両面の残留ガリウム層3を除去したのちに、更にクラスターサイズと1原子あたりの入射エネルギーの組み合わせを最適化したイオンドーズ量1014ions/cm2〜1016ions/cm2、加速電圧10〜20kVのアルゴン等の希ガスのガスクラスターイオンビーム1を、残留ガリウム層除去後の薄片2の表面に照射走査し(図1(d))、100〜200kVの電子線が透過する100nm以下まで更に薄片化する(図1(e))。膜厚の確認は原子間力顕微鏡等で適宜取り出して行う。 When measuring the dopant profile using electron holography, after removing the residual gallium layer 3 on both sides, the ion dose is optimized by combining the cluster size and incident energy per atom 10 14 ions / cm The surface of the thin piece 2 after removing the residual gallium layer is irradiated and scanned with a gas cluster ion beam 1 of a rare gas such as argon having 2 to 10 16 ions / cm 2 and an acceleration voltage of 10 to 20 kV (FIG. 1 (d)), It is further thinned to 100 nm or less through which an electron beam of 100 to 200 kV is transmitted (FIG. 1 (e)). The film thickness is confirmed by taking it out with an atomic force microscope or the like.
残留ガリウム層除去や薄片化の粗加工を、SF6やCF4のような反応性ガスクラスターイオンビームの増速効果のあるスパッタで行い、仕上げ加工をアルゴン等の希ガスのガスクラスターイオンビーム1で行えば加工時間を短くすることができる。 Residual gallium layer removal and slicing roughing are performed by sputtering with the effect of accelerating reactive gas cluster ion beams such as SF 6 and CF 4 , and finishing processing is performed by a gas cluster ion beam of rare gas such as argon 1 If this is done, the processing time can be shortened.
図2は、集束イオンビーム装置で切り出した薄片6から、ガスクラスターイオンビームで、走査キャパシタンス顕微鏡のためのドーパントプロファイル測定用サンプルを作製する場合の薄片6の処理工程毎の概略断面図である。
FIG. 2 is a schematic cross-sectional view for each processing step of the
残留ガリウム層3を除去するために、クラスターサイズと1原子あたりの入射エネルギーの組み合わせを最適化したイオンドーズ量1014ions/cm2〜1016ions/cm2、加速電圧10〜20kVのアルゴン等の希ガスのガスクラスターイオンビーム1を照射する(図2(a))。 In order to remove the residual gallium layer 3, an ion dose of 10 14 ions / cm 2 to 10 16 ions / cm 2 with optimized combination of cluster size and incident energy per atom, argon with an acceleration voltage of 10 to 20 kV, etc. Irradiate the gas cluster ion beam 1 of the rare gas (Fig. 2 (a)).
残留ガリウム層3の除去後、残留ガリウム除去後の薄片2の表面にクラスターイオンサイズ250以上、イオンドーズ量5X1015ions/cm2程度、加速電圧5〜10kVの酸素ガスクラスターイオンビーム5を照射し(図2(b))、残留ガリウム除去後の薄片2の断面に5〜10nm表面酸化層4を形成する(図2(c))。 After the removal of the residual gallium layer 3, the surface of the thin film 2 after the removal of the residual gallium 2 is irradiated with an oxygen gas cluster ion beam 5 having a cluster ion size of 250 or more, an ion dose of about 5 × 10 15 ions / cm 2 and an acceleration voltage of 5 to 10 kV. (FIG. 2 (b)), a 5 to 10 nm surface oxide layer 4 is formed on the cross section of the thin piece 2 after the removal of residual gallium (FIG. 2 (c)).
集束イオンビーム装置で、半導体デバイスの故障箇所の断面を含む薄片試料を切り出す。半導体デバイスの故障箇所は、対象となるチップに対しLSIテスタ、電子ビームテスタ等で測定される。切り出した薄片試料の断面を、走査キャパシタンス顕微鏡や電子線ホログラフィーでドーパントプロファイルを測定することでスパイク欠陥等の故障原因を明らかにすることもできる。 A thin sample including a cross section of a failure portion of the semiconductor device is cut out by the focused ion beam apparatus. The failure location of a semiconductor device is measured with an LSI tester, an electron beam tester or the like on the target chip. The cause of a failure such as a spike defect can be clarified by measuring the dopant profile of the cut-out slice sample with a scanning capacitance microscope or electron holography.
本方法は、走査キャパシタンス顕微鏡によるドーパントプロファイル測定用サンプル作製だけでなく、走査キャパシタンス顕微鏡よりも感度の高い走査非線形誘電率顕微鏡(SNDM)によるドーパントプロファイル測定のサンプル作製にも利用できる。 This method can be used not only for preparing a sample for measuring a dopant profile with a scanning capacitance microscope but also for preparing a sample for measuring a dopant profile with a scanning nonlinear dielectric microscope (SNDM), which is more sensitive than a scanning capacitance microscope.
1 アルゴンガスクラスターイオンビーム
2 残留ガリウム層を除去した薄片
3 残留ガリウム層
4 酸化膜
5 酸素ガスクラスターイオンビーム
6 集束イオンビーム装置で切り出した薄片
1 Argon gas cluster ion beam
2 Thin section from which residual gallium layer has been removed
3 Residual gallium layer
4 Oxide film
5 Oxygen gas cluster ion beam
6 Thin section cut out by focused ion beam device
Claims (5)
該切り出した薄片の残留ガリウム除去をガスクラスターイオンビームで行う工程を有するドーパントプロファイル測定用薄片試料作成方法。 Cutting out a slice including a desired cross section from a semiconductor device using a focused ion beam apparatus;
A method for preparing a flake sample for measuring a dopant profile, comprising a step of removing residual gallium from the cut flake with a gas cluster ion beam.
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Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2000230891A (en) * | 1999-02-09 | 2000-08-22 | Fuji Electric Co Ltd | Method for preparing sample for transmission type electron microscope |
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JP2000230891A (en) * | 1999-02-09 | 2000-08-22 | Fuji Electric Co Ltd | Method for preparing sample for transmission type electron microscope |
JP2003505867A (en) * | 1999-07-19 | 2003-02-12 | エピオン コーポレイション | Adaptive GCIB for surface smoothing |
JP2002277364A (en) * | 2001-03-19 | 2002-09-25 | Seiko Epson Corp | Method of working thin sample piece, and method of preparing thin sample piece |
JP2002298774A (en) * | 2001-03-29 | 2002-10-11 | Toshiba Corp | Electron microscope |
JP2004047315A (en) * | 2002-07-12 | 2004-02-12 | Seiko Instruments Inc | Ion beam device, ion beam machining method and holder member |
JP2004191358A (en) * | 2002-11-27 | 2004-07-08 | Seiko Instruments Inc | Sample preparation method and device by composite charge particle beam |
JP2004260137A (en) * | 2002-12-06 | 2004-09-16 | Soi Tec Silicon On Insulator Technologies | Method for recycling substrate |
JP2004226079A (en) * | 2003-01-20 | 2004-08-12 | Seiko Instruments Inc | Surface or section processing observation method and its device |
JP2004264145A (en) * | 2003-02-28 | 2004-09-24 | Toshiba Corp | Method for making transmission electron microscope observation specimen |
JP2005175369A (en) * | 2003-12-15 | 2005-06-30 | Japan Aviation Electronics Industry Ltd | Dry etching method and photonic crystal element produced using same |
JP2006093445A (en) * | 2004-09-24 | 2006-04-06 | Toshiba Corp | Oxide film forming method |
JP2006098189A (en) * | 2004-09-29 | 2006-04-13 | Jeol Ltd | Method and apparatus for producing sample |
JP2007108105A (en) * | 2005-10-17 | 2007-04-26 | Renesas Technology Corp | Method for preparing sample for electron microscope, converged ion beam device and a sample support stand |
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