JP2861776B2 - Semiconductor wafer with protective film - Google Patents
Semiconductor wafer with protective filmInfo
- Publication number
- JP2861776B2 JP2861776B2 JP33718793A JP33718793A JP2861776B2 JP 2861776 B2 JP2861776 B2 JP 2861776B2 JP 33718793 A JP33718793 A JP 33718793A JP 33718793 A JP33718793 A JP 33718793A JP 2861776 B2 JP2861776 B2 JP 2861776B2
- Authority
- JP
- Japan
- Prior art keywords
- wafer
- film
- protective film
- semiconductor
- semiconductor wafer
- 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.)
- Expired - Fee Related
Links
- 239000004065 semiconductor Substances 0.000 title claims description 29
- 230000001681 protective effect Effects 0.000 title claims description 20
- 229920006254 polymer film Polymers 0.000 claims description 15
- 150000001875 compounds Chemical class 0.000 claims description 12
- 239000002052 molecular layer Substances 0.000 claims description 8
- 229910001218 Gallium arsenide Inorganic materials 0.000 claims description 6
- 235000012431 wafers Nutrition 0.000 description 58
- 239000010408 film Substances 0.000 description 30
- 238000000034 method Methods 0.000 description 15
- 238000004140 cleaning Methods 0.000 description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 9
- 239000013078 crystal Substances 0.000 description 8
- 238000005498 polishing Methods 0.000 description 7
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 238000010586 diagram Methods 0.000 description 5
- 238000005468 ion implantation Methods 0.000 description 5
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 4
- 238000005530 etching Methods 0.000 description 4
- 238000001451 molecular beam epitaxy Methods 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 3
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 3
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 3
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
- 239000005642 Oleic acid Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 3
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 3
- 239000011241 protective layer Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 238000004611 spectroscopical analysis Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000010301 surface-oxidation reaction Methods 0.000 description 2
- 230000005533 two-dimensional electron gas Effects 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- PDHVYEMYFOJVIN-QURGRASLSA-N CCCCCCCCCCCCCCCCCCCC\C=C\C(O)=O Chemical compound CCCCCCCCCCCCCCCCCCCC\C=C\C(O)=O PDHVYEMYFOJVIN-QURGRASLSA-N 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- RBFQJDQYXXHULB-UHFFFAOYSA-N arsane Chemical compound [AsH3] RBFQJDQYXXHULB-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 230000005669 field effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- -1 polypropylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229910021642 ultra pure water Inorganic materials 0.000 description 1
- 239000012498 ultrapure water Substances 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
Landscapes
- Physical Deposition Of Substances That Are Components Of Semiconductor Devices (AREA)
- Cleaning Or Drying Semiconductors (AREA)
- Formation Of Insulating Films (AREA)
Description
【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION
【0001】[0001]
【産業上の利用分野】本発明は保護膜付き半導体ウェハ
に係り、特にLB膜と高分子膜とを用いてウェハ表面の
保護を図ったものに関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a semiconductor wafer having a protective film, and more particularly to a semiconductor wafer having an LB film and a polymer film for protecting the surface of the wafer.
【0002】[0002]
【従来の技術】化合物半導体はショットキーゲート電界
効果トランジスタ(MESFET)、高移動度トランジ
スタ(HEMT)、ヘテロ接合バイポーラトランジスタ
(HBT)等の他、種々の受発光デバイスの作製に用い
られている。これらの素子は鏡面ウェハ表面に分子線エ
ピタキシャル成長(MBE)法、有機金属気相エピタキ
シャル成長(MOVPE)法およびイオン打ち込み法等
により能動層を作成する。鏡面ウェハは次の手順で作成
される。2. Description of the Related Art Compound semiconductors are used in the manufacture of various light emitting and receiving devices, such as a Schottky gate field effect transistor (MESFET), a high mobility transistor (HEMT), a heterojunction bipolar transistor (HBT), and the like. In these devices, an active layer is formed on a mirror-finished wafer surface by a molecular beam epitaxial growth (MBE) method, a metal organic vapor phase epitaxial growth (MOVPE) method, an ion implantation method, or the like. A mirror wafer is created by the following procedure.
【0003】インゴットをスライスし、ウェハを切り出
す。このウェハを粗研磨し平坦性を高めた後、メカノケ
ミカル研磨により鏡面に仕上げる。次に脱脂洗浄、極く
わずかなエッチング作用を持つ洗浄液での洗浄および超
純水洗浄を行う。最後にウェハをIPA(イソプロピー
ルアルコール)乾燥法またはスピン乾燥法により乾燥す
る。[0003] An ingot is sliced and a wafer is cut out. This wafer is roughly polished to improve its flatness, and then mirror-finished by mechanochemical polishing. Next, degreasing cleaning, cleaning with a cleaning liquid having an extremely slight etching effect, and ultrapure water cleaning are performed. Finally, the wafer is dried by an IPA (isopropyl alcohol) drying method or a spin drying method.
【0004】このウェハは、不活性ガスを封入したウェ
ハトレイに個装され、保管される。この保管されたウェ
ハをエピタキシャル成長やイオン打ち込みに使用するに
際して、有機洗浄やエッチングなどの前処理を必ず行
い、ウェハ表面の有機物、酸化物を除去する。The wafer is individually mounted on a wafer tray filled with an inert gas and stored. When this stored wafer is used for epitaxial growth or ion implantation, pretreatment such as organic cleaning and etching is always performed to remove organic substances and oxides on the wafer surface.
【0005】[0005]
【発明が解決しようとする課題】ウェハ表面には活性な
未結合手が存在するため、保管したウェハ表面は有機物
などの不純物汚染や酸化物の生成により劣化する。その
ために、結晶のエピタキシャル成長やイオン打ち込みの
前には、不純物や酸化物除去のために、必ず洗浄やエッ
チングなどの前処理を行わなければならなかった。とこ
ろが、この前処理は煩雑な作業であり、また安定した処
理ではなく、かえって表面を汚染したり、表面の平坦性
を悪化させるという問題点があった。Since active dangling bonds are present on the wafer surface, the stored wafer surface is deteriorated by impurity contamination such as organic substances and the formation of oxides. Therefore, prior to the epitaxial growth of the crystal or ion implantation, a pretreatment such as cleaning or etching must be performed to remove impurities and oxides. However, this pretreatment is a complicated operation and is not a stable treatment, but rather has the problem of contaminating the surface and deteriorating the flatness of the surface.
【0006】具体的には、例えばMBE法でエピタキシ
ャル成長する場合、成長前にウェハ表面を数μm 程度エ
ッチングした後、MBE炉内で熱処理によりウェハ表面
の清浄化を行なう必要があるが、エッチャントの取り扱
いが面倒であり、また、炉内でのサーマルクリーニング
が完全に行なえなかったり、クリーニングに時間がかか
ったり、時間が安定しなかったりする上、ウェハ表面の
酸化物が残留し、その後のエピタキシャル成長において
良好な結晶成長ができないことが多かった。Specifically, for example, when epitaxial growth is performed by MBE, it is necessary to etch the wafer surface by about several μm before growth and then clean the wafer surface by heat treatment in an MBE furnace. In addition, thermal cleaning in the furnace cannot be completely performed, cleaning takes time, and the time is not stable.In addition, oxides on the wafer surface remain, which is good in subsequent epitaxial growth. In many cases, crystal growth was not possible.
【0007】本発明の目的は、保護性と剥離性の良好な
保護膜でウェハ表面を被覆することによって、前記した
従来技術の欠点を解消し、洗浄やエッチング等の前処理
をすることなく、高品質なエピタキシャル結晶やイオン
打ち込み層が得られる新規な保護膜付き半導体ウェハを
提供することにある。An object of the present invention is to solve the above-mentioned drawbacks of the prior art by coating the wafer surface with a protective film having good protective properties and peeling properties, without performing pretreatment such as cleaning and etching. It is an object of the present invention to provide a novel semiconductor wafer with a protective film capable of obtaining a high-quality epitaxial crystal and an ion-implanted layer.
【0008】[0008]
【課題を解決するための手段】本発明の保護膜付き半導
体ウェハは、表面に分子層レベルのLB膜を形成し、そ
の上に高分子膜を被覆したものである。表面保護膜をL
B膜と高分子膜との2層で構成したのは、LB膜のみだ
と薄すぎるため、また高分子膜のみだと結合が強すぎる
ため、共にウェハ表面から剥がすのが難しいからであ
る。The semiconductor wafer with a protective film according to the present invention is obtained by forming an LB film on the surface of a molecular layer on the surface and coating the polymer film on the LB film. L for surface protective film
The reason why the two layers of the B film and the polymer film are used is that the LB film alone is too thin, and the polymer film alone is too strong in bonding, so that it is difficult to peel off both from the wafer surface.
【0009】なお、分子層レベルとは1分子層、または
2以上の分子層をいう。LB膜としては、ポリイミド、
ステアリン酸、トリコセン酸等様々なものがある。薄膜
を分子レベルで制御できるものなら特に制限はない。ま
た、高分子膜としては、塩化ビニル、セロハン、ポリプ
ロピレン等様々なものがある。数十μm 〜数mmの膜膜で
あれば、特に制限はない。[0009] The molecular layer level means one molecular layer or two or more molecular layers. As the LB film, polyimide,
There are various things such as stearic acid and tricosenoic acid. There is no particular limitation as long as the thin film can be controlled at the molecular level. In addition, there are various polymer films such as vinyl chloride, cellophane, and polypropylene. There is no particular limitation as long as the film has a thickness of several tens μm to several mm.
【0010】また、半導体はSiまたは化合物半導体等
であり、化合物半導体はIII −V族族化合物半導体等で
あり、さらにIII −V族化合物半導体はGaAsやIn
P等である。The semiconductor is Si or a compound semiconductor, the compound semiconductor is a group III-V compound semiconductor, and the group III-V compound semiconductor is GaAs or Indium.
P and the like.
【0011】[0011]
【作用】図1を用いて説明する。研磨、洗浄、乾燥後の
ウェハ2の表面3には活性な未結合手1が存在する(図
1(a))。このウェハ表面3にLB膜4を1分子層形
成することにより、ウェハ表面3の未結合手1が不活性
化される(図1(b))。The operation will be described with reference to FIG. Active dangling bonds 1 are present on the surface 3 of the wafer 2 after polishing, cleaning and drying (FIG. 1A). By forming one molecular layer of the LB film 4 on the wafer surface 3, the dangling bonds 1 on the wafer surface 3 are inactivated (FIG. 1B).
【0012】さらにLB膜4の上に高分子膜5を圧着す
ると、LB膜4の分子端と高分子膜5が結合して表面保
護膜が形成される(図1(c))。その結果、保管中の
ウェハ表面3への不純物の付着、酸素や水分による表面
酸化が抑止される。When the polymer film 5 is further pressed onto the LB film 4, the molecular ends of the LB film 4 and the polymer film 5 are bonded to form a surface protective film (FIG. 1C). As a result, adhesion of impurities to the wafer surface 3 during storage and surface oxidation by oxygen and moisture are suppressed.
【0013】LB膜4と高分子膜5の結合は、LB膜4
とウェハ表面3の結合に比較してかなり強いので、高分
子膜5を機械的に剥がすだけでウェハ表面3とLB膜4
の界面で剥がれ、清浄なウェハ表面3が得られる(図1
(d))。The connection between the LB film 4 and the polymer film 5
Is significantly stronger than the bond between the wafer surface 3 and the wafer surface 3.
, And a clean wafer surface 3 is obtained.
(D)).
【0014】したがって、エピタキシャル成長やイオン
打ち込みの前に、このLB膜4と高分子膜5からなる保
護膜を剥がすことにより、清浄なウェハ表面3が容易に
得られ、洗浄、エッチングなどの特別な前処理をするこ
となく、良好なエピタキシャル結晶やイオン打ち込み層
が得られる。Therefore, before the epitaxial growth or ion implantation, the protective film composed of the LB film 4 and the polymer film 5 is peeled off, so that a clean wafer surface 3 can be easily obtained. A good epitaxial crystal or ion-implanted layer can be obtained without any treatment.
【0015】なお、LB膜の付着法としては、垂直侵漬
法、水平付着法、ムービングウォール法などの湿式処
理、蒸着法による乾式処理等、任意の方法を用いること
ができる。The LB film can be attached by any method such as a wet treatment such as a vertical immersion method, a horizontal attachment method, a moving wall method, and a dry treatment by a vapor deposition method.
【0016】[0016]
【実施例】以下、本発明の保護膜付き半導体ウェハの実
施例を説明する。ここでは半導体ウェハとしてGaAs
結晶ウェハについて説明するが、SiやInP等にも共
通する。Embodiments of the present invention will be described below with reference to the accompanying drawings. Here, GaAs is used as the semiconductor wafer.
A crystal wafer will be described, but is common to Si, InP, and the like.
【0017】<実施例1>研磨、洗浄、乾燥後のGaA
s結晶ウェハ表面に、垂直浸漬法によりオレイン酸から
なる1分子層のLB膜を形成した。次に、その上から厚
さ100μm の塩化ビニルシートを圧着した。このウェ
ハを大気中に1カ月から12カ月放置した。各期間放置
後、ウェハ表面のシートを機械的に剥がし、表面のオー
ジェ電子分光分析を行った。<Example 1> GaAs after polishing, washing and drying
A single molecular layer LB film made of oleic acid was formed on the surface of the s-crystal wafer by a vertical immersion method. Next, a vinyl chloride sheet having a thickness of 100 μm was pressed thereon. The wafer was left in the atmosphere for 1 to 12 months. After being left for each period, the sheet on the wafer surface was mechanically peeled off, and Auger electron spectroscopic analysis of the surface was performed.
【0018】比較試料として、研磨、洗浄、乾燥後、窒
素封入したウェハトレイに個装したものも作成し、同期
間放置後、表面のO,Cのオージェ電子分光分析を行な
った。オージェ分析結果を図2、3に示す。研磨洗浄
後、窒素中で保管したものは、O、Cともに増加し、有
機物汚染および表面酸化が認められたが、本実施例の保
護層をつけたものには、O,C共にほとんど増加してお
らず、清浄な表面を保っていた。As a comparative sample, a sample which was individually polished, washed, dried and mounted individually on a wafer tray filled with nitrogen was also prepared. After being left for the same period, Auger electron spectroscopic analysis of O and C on the surface was performed. The Auger analysis results are shown in FIGS. After polishing and cleaning, those stored in nitrogen increased both O and C, and organic contamination and surface oxidation were observed. However, those with the protective layer of this example showed almost all increase in O and C. And kept a clean surface.
【0019】<実施例2>研磨、洗浄、乾燥後のGaA
s結晶ウェハ表面にオレイン酸を垂直浸漬法により、1
分子層形成した。次に、厚さ100μm の塩化ビニルシ
ートを圧着した。このウェハを大気中に1カ月から12
カ月放置した。各期間放置後、ウェハ表面のシートを剥
がし、分子線エピタキシャル(MBE)成長により、H
EMTを成長した。その電気特性を77Kにて評価し
た。Example 2 GaAs after polishing, cleaning and drying
Oleic acid was vertically immersed on the surface of the
A molecular layer was formed. Next, a vinyl chloride sheet having a thickness of 100 μm was pressed. Place this wafer in air for one month to 12
Left for months. After being left for each period, the sheet on the wafer surface is peeled off, and H is grown by molecular beam epitaxy (MBE).
EMT was grown. The electrical characteristics were evaluated at 77K.
【0020】比較のために、研磨、洗浄、乾燥後、窒素
封入したウェハトレイに個装したものについても同様の
実験を行った。なお、比較例は前処理をしていない。結
果を図4に示す。研磨洗浄後、窒素中で保管したウェハ
の2次元電子ガスの移動度は、保管期間が長くなると共
に低下していくが、本発明の保護層をつけたものには、
低下は認められなかった。For comparison, a similar experiment was carried out for wafers individually polished, washed, dried, and mounted on a wafer tray sealed with nitrogen. Note that the comparative example was not pre-processed. FIG. 4 shows the results. After polishing and cleaning, the mobility of the two-dimensional electron gas of the wafer stored in nitrogen decreases as the storage period increases, but the one provided with the protective layer of the present invention includes:
No decrease was observed.
【0021】<実施例3>研磨、洗浄、乾燥後のGaA
s結晶ウェハにオレイン酸を垂直浸漬法により、1分子
層形成した。次に、厚さ100μm の塩化ビニルシート
を圧着した。このウェハを大気中に1カ月から12カ月
放置した。各期間放置後、ウェハ表面のシートを剥が
し、イオン打ち込みを行った。Siイオンを打ち込み、
アルシン雰囲気でアニールし、渦電流法でシート抵抗を
調べた。<Example 3> GaAs after polishing, washing and drying
Oleic acid was formed in one molecular layer on the s-crystal wafer by a vertical dipping method. Next, a vinyl chloride sheet having a thickness of 100 μm was pressed. The wafer was left in the atmosphere for 1 to 12 months. After being left for each period, the sheet on the wafer surface was peeled off and ion implantation was performed. Implant Si ions,
After annealing in an arsine atmosphere, the sheet resistance was examined by the eddy current method.
【0022】比較のために、研磨、洗浄、乾燥後、窒素
封入したウェハトレイに個装したものについても同様の
実験を行った。なお、比較例は前処理をしていない。保
管期間とシート抵抗の関係を図5に示す。窒素中で保管
したウェハのシート抵抗は、保管期間が長くなると共に
増大し、活性化率が低下していた。本発明の保護層をつ
けたウェハのシート抵抗はほとんど変化していなかっ
た。For comparison, a similar experiment was carried out for wafers individually polished, washed, dried, and mounted on a wafer tray sealed with nitrogen. Note that the comparative example was not pre-processed. FIG. 5 shows the relationship between the storage period and the sheet resistance. The sheet resistance of the wafer stored in nitrogen increased with the storage period, and the activation rate decreased. The sheet resistance of the wafer provided with the protective layer of the present invention hardly changed.
【0023】[0023]
(1) 請求項1及び2に記載の発明によれば、LB膜と高
分子膜とからなる表面保護膜でウェハ表面を被覆するよ
うにしたので、ウェハ表面の経時劣化を有効に抑止する
ことができる。使用に際しては、LB膜の上に高分子膜
を被覆してあるので、高分子膜を剥がすだけで簡単かつ
極く短時間で清浄表面が得られる。そのため、ウェハ保
管にあたって特別な梱包を要せず、経済的に有利であ
る。(1) According to the first and second aspects of the present invention, the surface of the wafer is covered with the surface protective film composed of the LB film and the polymer film. Can be. In use, since the polymer film is coated on the LB film, a clean surface can be obtained simply and in a very short time only by peeling the polymer film. Therefore, no special packing is required for storing the wafer, which is economically advantageous.
【0024】また長期保管したウェハにおいても、なん
ら特別な前処理することなく高品質なエピタキシャル結
晶、イオン打ち込み層を安定して得られるため、プロセ
ス時間を短縮し、歩留を向上することができる。Further, even for a wafer stored for a long period of time, a high-quality epitaxial crystal and ion-implanted layer can be stably obtained without any special pretreatment, so that the process time can be shortened and the yield can be improved. .
【0025】さらにLB膜形成および高分子膜の被覆
は、いずれも簡便な方法であり、高価な装置を要さず、
経済的に有利である。Further, the formation of the LB film and the coating of the polymer film are both simple methods and do not require expensive equipment.
Economically advantageous.
【0026】(2) 請求項3ないし6に記載の発明によれ
ば、特に表面が不安定な化合物半導体ウェハの保護が図
れるので、化合物半導体製品の品質を高めることができ
る。(2) According to the third to sixth aspects of the present invention, particularly, the compound semiconductor wafer having an unstable surface can be protected, so that the quality of the compound semiconductor product can be improved.
【図1】本発明の保護膜付き半導体ウェハの実施例を説
明するための保護膜形成方法の工程図。FIG. 1 is a process diagram of a protective film forming method for explaining an embodiment of a semiconductor wafer with a protective film according to the present invention.
【図2】保護膜を付けた第1実施例と比較例とにおける
ウェハ表面のOの経時変化を示す比較特性図。FIG. 2 is a comparative characteristic diagram showing a change over time of O on the wafer surface between the first embodiment having a protective film and a comparative example.
【図3】保護膜を付けた第1実施例と比較例とにおける
ウェハ表面のCの経時変化を示す比較特性図。FIG. 3 is a comparative characteristic diagram showing a change over time of C on a wafer surface between the first embodiment having a protective film and a comparative example.
【図4】ウェハ表面にHEMTを成長した第2実施例と
比較例とにおける2次元電子ガス移動度の経時変化を示
す比較特性図。FIG. 4 is a comparison characteristic diagram showing a change over time in two-dimensional electron gas mobility in a second embodiment in which HEMT is grown on a wafer surface and a comparative example.
【図5】ウェハ表面にイオンを打ち込んだ第3実施例と
比較例とにおけるシート抵抗の経時変化を示す比較特性
図。FIG. 5 is a comparison characteristic diagram showing a change over time in sheet resistance between the third example in which ions are implanted into the wafer surface and a comparative example.
1 未結合手 2 ウェハ 3 ウェハ表面 4 LB(ラングミュア・ブロジェット)膜 5 高分子膜 DESCRIPTION OF SYMBOLS 1 Unbonded hand 2 Wafer 3 Wafer surface 4 LB (Langmuir-Blodgett) film 5 Polymer film
Claims (6)
ジェット(LB)膜を形成し、その上に高分子膜を被覆
した保護膜付き半導体ウェハ。1. A semiconductor wafer provided with a protective film in which a Langmuir-Projet (LB) film at the molecular layer level is formed on the surface and a polymer film is coated thereon.
保護膜付き半導体ウェハ。2. The semiconductor wafer with a protective film according to claim 1, wherein said semiconductor is Si.
に記載の保護膜付き半導体ウェハ。3. The semiconductor device according to claim 1, wherein said semiconductor is a compound semiconductor.
4. The semiconductor wafer with a protective film according to 1.
導体である請求項3に記載の保護膜付き半導体ウェハ。4. The semiconductor wafer with a protective film according to claim 3, wherein said compound semiconductor is a III-V group compound semiconductor.
ある請求項4に記載の保護膜付き半導体ウェハ。5. The semiconductor wafer with a protective film according to claim 4, wherein said III-V compound semiconductor is GaAs.
る請求項1に記載の保護膜付き半導体ウェハ。6. The semiconductor wafer with a protective film according to claim 1, wherein said III-V compound semiconductor is InP.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP33718793A JP2861776B2 (en) | 1993-12-28 | 1993-12-28 | Semiconductor wafer with protective film |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP33718793A JP2861776B2 (en) | 1993-12-28 | 1993-12-28 | Semiconductor wafer with protective film |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH07201689A JPH07201689A (en) | 1995-08-04 |
| JP2861776B2 true JP2861776B2 (en) | 1999-02-24 |
Family
ID=18306272
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP33718793A Expired - Fee Related JP2861776B2 (en) | 1993-12-28 | 1993-12-28 | Semiconductor wafer with protective film |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2861776B2 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4207976B2 (en) | 2006-05-17 | 2009-01-14 | 住友電気工業株式会社 | Method for surface treatment of compound semiconductor substrate and method for producing compound semiconductor crystal |
| JP4614330B2 (en) * | 2005-01-31 | 2011-01-19 | 独立行政法人科学技術振興機構 | Method for producing silicon substrate modified with organic group |
| JP5276281B2 (en) | 2007-06-01 | 2013-08-28 | 住友電気工業株式会社 | GaAs semiconductor substrate and manufacturing method thereof |
| US7932179B2 (en) | 2007-07-27 | 2011-04-26 | Micron Technology, Inc. | Method for fabricating semiconductor device having backside redistribution layers |
| CN107039516B (en) * | 2011-05-18 | 2020-07-10 | 住友电气工业株式会社 | Compound semiconductor substrate |
-
1993
- 1993-12-28 JP JP33718793A patent/JP2861776B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH07201689A (en) | 1995-08-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US10083855B2 (en) | Method of manufacturing high resistivity SOI wafers with charge trapping layers based on terminated Si deposition | |
| JP3093904B2 (en) | Method for growing compound semiconductor crystal | |
| US3969164A (en) | Native oxide technique for preparing clean substrate surfaces | |
| GB2024506A (en) | Ohmic contacts to n-type group iii-v semiconductors | |
| WO2013186749A1 (en) | Method for depositing a group iii nitride semiconductor film | |
| TWI601855B (en) | Method of depositing an aluminum nitride layer | |
| US5402748A (en) | Method of growing a compound semiconductor film | |
| JP2861776B2 (en) | Semiconductor wafer with protective film | |
| KR20070044441A (en) | Interfacial layer used with high dielectric material | |
| JP2004519837A (en) | Epitaxial wafer equipment | |
| JPH06120163A (en) | Forming of electrode of semiconductor device | |
| JPH08335695A (en) | Compound semiconductor device and manufacturing method thereof | |
| US11031507B2 (en) | Semiconductor device and method of manufacture | |
| JP3466365B2 (en) | Semiconductor substrate manufacturing method | |
| KR20060003037A (en) | Compound semiconductor epitaxial substrate | |
| JP3153270B2 (en) | Surface coating treatment method in crystal growth method | |
| JPH0194662A (en) | Manufacture of mis type semiconductor using gallium arsenide | |
| JPS62115831A (en) | Manufacture of semiconductor device | |
| King et al. | Ex situ and in situ methods for complete oxygen and non-carbidic carbon removal from (0001) Si 6H-SiC surfaces | |
| JPS61145823A (en) | Molecular beam epitaxial growth method | |
| JP2005019580A (en) | Cleaning and drying method for semiconductor wafer packing materials | |
| JPH10284512A (en) | Method for manufacturing II-VI compound semiconductor single crystal wafer and II-VI compound semiconductor single crystal wafer | |
| JPH03131593A (en) | Preliminary treatment of substrate for epitaxial grow | |
| JPH08153683A (en) | Compound semiconductor device on silicon substrate and manufacturing method thereof | |
| JPH0521476A (en) | Method for manufacturing II-VI compound semiconductor |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |