JPS63205908A - Plating method for semiconductor substrate - Google Patents
Plating method for semiconductor substrateInfo
- Publication number
- JPS63205908A JPS63205908A JP3806287A JP3806287A JPS63205908A JP S63205908 A JPS63205908 A JP S63205908A JP 3806287 A JP3806287 A JP 3806287A JP 3806287 A JP3806287 A JP 3806287A JP S63205908 A JPS63205908 A JP S63205908A
- Authority
- JP
- Japan
- Prior art keywords
- copper
- polished
- acid
- diffusion depth
- solution
- 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.)
- Pending
Links
- 238000007747 plating Methods 0.000 title claims abstract description 17
- 239000004065 semiconductor Substances 0.000 title claims abstract description 11
- 239000000758 substrate Substances 0.000 title claims abstract description 10
- 238000000034 method Methods 0.000 title claims description 11
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 17
- 229910052802 copper Inorganic materials 0.000 claims abstract description 17
- 239000010949 copper Substances 0.000 claims abstract description 17
- 239000002253 acid Substances 0.000 claims abstract description 12
- 239000000243 solution Substances 0.000 claims abstract description 9
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 claims abstract description 8
- 239000012670 alkaline solution Substances 0.000 claims abstract description 7
- 229910000365 copper sulfate Inorganic materials 0.000 claims abstract description 5
- 239000012298 atmosphere Substances 0.000 claims abstract description 3
- 238000010438 heat treatment Methods 0.000 claims abstract description 3
- 238000007654 immersion Methods 0.000 claims description 2
- 238000009792 diffusion process Methods 0.000 abstract description 18
- 239000012535 impurity Substances 0.000 abstract description 13
- 230000005855 radiation Effects 0.000 abstract 2
- 238000002791 soaking Methods 0.000 abstract 1
- 235000012431 wafers Nutrition 0.000 description 27
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 21
- 229910052710 silicon Inorganic materials 0.000 description 21
- 239000010703 silicon Substances 0.000 description 21
- 239000000853 adhesive Substances 0.000 description 17
- 230000001070 adhesive effect Effects 0.000 description 17
- 239000008188 pellet Substances 0.000 description 12
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 238000005259 measurement Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000000691 measurement method Methods 0.000 description 2
- DDFHBQSCUXNBSA-UHFFFAOYSA-N 5-(5-carboxythiophen-2-yl)thiophene-2-carboxylic acid Chemical compound S1C(C(=O)O)=CC=C1C1=CC=C(C(O)=O)S1 DDFHBQSCUXNBSA-UHFFFAOYSA-N 0.000 description 1
- 241000257465 Echinoidea Species 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- QZPSXPBJTPJTSZ-UHFFFAOYSA-N aqua regia Chemical compound Cl.O[N+]([O-])=O QZPSXPBJTPJTSZ-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
Landscapes
- Sampling And Sample Adjustment (AREA)
- Testing Or Measuring Of Semiconductors Or The Like (AREA)
Abstract
Description
【発明の詳細な説明】
〔発明の目的〕
(産業上の利用分野)
この発明は直接接着法により作成した半導体基板のメッ
キ法に関する。DETAILED DESCRIPTION OF THE INVENTION [Object of the Invention] (Industrial Application Field) This invention relates to a method of plating a semiconductor substrate made by a direct bonding method.
(従来の技術)
一般にシリコンウニ八同士を接着剤を用いることなく、
直接接着した接着シリコンウェハにおいて、接着界面を
横切る不純物の拡散深さく接着界面とpn接合面との距
離)の測定は半導体デバイスの製造プロセスにおいて重
要である。(Prior art) Generally, silicon sea urchins are bonded together without using adhesive.
In directly bonded bonded silicon wafers, measurement of the diffusion depth of impurities across the bonding interface (the distance between the bonding interface and the pn junction surface) is important in the semiconductor device manufacturing process.
従来の未接着シリコンウェハにおける拡散深さの測定は
、抵抗スプレディング法、メッキ法、エツチング法など
により測定することができる。しかし、接着シリコンウ
ェハは接着界面を持つウェハのために、前記した従来の
測定法では、接着界面を横切る不純物の拡散深さを精度
よく測定することは困難であった。それは、接着ウェハ
の接着界面とpn接合面を同時に検出して評価すること
ができないためである。Diffusion depth in conventional unbonded silicon wafers can be measured by resistive spreading, plating, etching, or the like. However, since a bonded silicon wafer has an adhesive interface, it is difficult to accurately measure the diffusion depth of impurities across the adhesive interface using the conventional measurement method described above. This is because it is not possible to simultaneously detect and evaluate the bonding interface and the pn junction surface of the bonded wafer.
そこで1本発明者らは、新手法の銅メツキ法を考案した
。これにより、接着シリコンウェハの接着界面とpn接
合面を同時且つ明瞭に検出して、拡散深さを精度良く、
簡単に測定することができた。Therefore, the present inventors devised a new copper plating method. This enables simultaneous and clear detection of the bonding interface and pn junction surface of the bonded silicon wafer, and accurate measurement of the diffusion depth.
It was easy to measure.
(発明が解決しようとする間頭点)
従来における直接接着シリコンウェハの接着界面を横切
る不純物の拡散深さの測定は、接着界面とpn接合面を
同時且つ明瞭に検出しなければならないために、従来の
測定法では困鷺である。(The main problem to be solved by the invention) In the conventional measurement of the diffusion depth of impurities across the bonding interface of a directly bonded silicon wafer, the bonding interface and the pn junction surface must be detected simultaneously and clearly. This is difficult with conventional measurement methods.
本発明は直接接着シリコンウェハの拡散深さの測定にお
いて、接着界面とpn接合面を同時且つ明瞭に検出して
、不純物の拡散深さを精度良く簡単に測定するための半
導体基板のメッキ法を提供するものである。The present invention provides a semiconductor substrate plating method for measuring the diffusion depth of directly bonded silicon wafers by simultaneously and clearly detecting the bonding interface and the pn junction surface and easily measuring the diffusion depth of impurities with high accuracy. This is what we provide.
(問題点を解決するための手段)
本発明は、直接接着シリコンウェハの接着界面を横切る
不純物深さの測定において、角度研磨したウェハを酸ま
たはアルカリ溶液に浸漬させた後、光照射下の硫酸銅溶
液中で銅メッキする半導体基板のメッキ方法である。(Means for Solving the Problems) In the measurement of the impurity depth across the bonding interface of directly bonded silicon wafers, the present invention involves immersing the angle-polished wafer in an acid or alkaline solution and then using sulfuric acid under light irradiation. This is a plating method for semiconductor substrates in which copper is plated in a copper solution.
(作 用)
本発明は接着シリコンウェハを光照射下の硫酸銅溶液中
で銅メッキする時、角度研磨した接着シリコンウェハを
銅メッキする前に、酸に浸漬させてから銅メッキした。(Function) In the present invention, when a bonded silicon wafer is copper-plated in a copper sulfate solution under light irradiation, the angle-polished bonded silicon wafer is immersed in acid and then copper-plated before being plated with copper.
このウェハは接着界面とpn接合面を同時且つ明瞭に検
出することができて、接着界面を横切る不純物の拡散深
さが精度よく簡単に測定できた。また、接着シリコンウ
ェハをアルカリ溶液に浸漬後、銅メッキした場合も酸の
時と同様な結果が得られた。In this wafer, the adhesive interface and the pn junction surface could be detected simultaneously and clearly, and the diffusion depth of impurities across the adhesive interface could be easily measured with high accuracy. Also, when a bonded silicon wafer was immersed in an alkaline solution and then plated with copper, results similar to those obtained with acid were obtained.
しかし、同様に角度研磨した接着シリコンウェハを酸ま
たは、アルカリ溶液に浸漬させることなく、銅メッキし
たウェハは、接着界面及びpn接合面共に不明瞭で検出
できないため、接着界面を横切る不純物の拡散深さの測
定は、不可能であった。この結果から、接着シリコンウ
ェハの接着界面を横切る不純物の拡散深さを銅メツキ法
により測定する時、接着シリコンウェハを酸または、ア
ルカリ溶液に浸漬させてから、銅メッキする方法は拡散
深さを測定するのに、ftN単で精度の良いメッキ法で
あることが判明した。However, when bonded silicon wafers are similarly angle-polished and copper plated without immersing them in acid or alkaline solutions, both the bonding interface and the pn junction surface are unclear and cannot be detected, resulting in the depth of impurity diffusion across the bonding interface. It was not possible to measure the From this result, when measuring the diffusion depth of impurities across the adhesive interface of a bonded silicon wafer using the copper plating method, the method of immersing the bonded silicon wafer in an acid or alkaline solution and then plating with copper will reduce the diffusion depth. It has been found that the plating method requires only ftN and has high accuracy for measurement.
(実施例)
第1の実施例
直径76mm、厚さ0.40mm、 P型面方位(10
0)、 比抵抗0.003Ω・cIl(Bドープ)のシ
リコンウェハと直径、厚さが同じN型、面方位(100
) 、 比抵抗7Ω・am(Pドープ)のシリコンウ
ェハを用いた。(Example) First example diameter: 76 mm, thickness: 0.40 mm, P-type surface orientation (10
0), N-type with the same diameter and thickness as a silicon wafer with a specific resistance of 0.003Ω・cIl (B-doped), and a surface orientation (100
), a silicon wafer with a specific resistance of 7 Ω·am (P-doped) was used.
二枚のウェハをトリクレン、アセレンの脱脂処理、過酸
化水素と硫酸の混酸処理そして王水処理後。Two wafers were degreased with trichlene and acelene, treated with a mixed acid of hydrogen peroxide and sulfuric acid, and treated with aqua regia.
水洗して乾燥した。このウェハをクラスlO以下の清浄
雰囲気下で鏡面同士を接触させて接着し、窒素雰囲気の
電気炉中で1100℃、5時間熱処理することにより一
体化した。この直接接着シリコンウェハから5 +om
X 10nv+のペレットを切り出し、5度44分の
角度研磨治具に固定して、接着界面が露出するように鏡
面研磨した。この研磨したペレットを少量の沸酸が添加
されている硫酸銅飽和溶液に15秒間浸漬させながら、
白熱電球(100W)で照らして、銅メッキ膜を析出さ
せ、水洗後、乾燥した。Washed with water and dried. The wafers were bonded with their mirror surfaces in contact with each other in a clean atmosphere of class 1O or lower, and integrated by heat treatment at 1100° C. for 5 hours in an electric furnace in a nitrogen atmosphere. 5+om from this direct bonded silicon wafer
A pellet of X 10nv+ was cut out, fixed to a polishing jig at an angle of 5 degrees and 44 minutes, and mirror-polished so that the adhesive interface was exposed. While immersing the polished pellets in a saturated copper sulfate solution to which a small amount of boiling acid has been added for 15 seconds,
A copper plating film was deposited by illuminating it with an incandescent light bulb (100 W), washed with water, and then dried.
このペレットの接着界面を顕微鏡で調べたが、接着界面
は検出できず、pn接合面は不明瞭であった。The adhesive interface of this pellet was examined under a microscope, but no adhesive interface could be detected and the pn junction surface was unclear.
しかし、同様に鏡面研磨したペレットを塩酸に3秒間、
浸漬させてから、前記と同様に硫酸銅飽和溶液に20秒
間浸漬させながら、ランプで照らして、銅メッキ膜を析
出させ、水洗後、乾燥した。However, similarly, mirror-polished pellets were soaked in hydrochloric acid for 3 seconds.
After immersion, the copper plating film was precipitated by immersing it in a copper sulfate saturated solution for 20 seconds and illuminating it with a lamp, followed by washing with water and drying.
このペレットの接着界面を顕微鏡で調べると、接着界面
及びpn接合面ともに明瞭に検出することができた。不
純物の拡散深さく接着界面とpn接合面の距離)の測定
値は計算値と14以内の精度で一致した。When the adhesive interface of this pellet was examined using a microscope, both the adhesive interface and the pn junction surface could be clearly detected. The measured values of the impurity diffusion depth (distance between the adhesive interface and the pn junction surface) agreed with the calculated values with an accuracy of within 14.
尚、研磨したペレットを沸酸に5秒間浸漬してから銅メ
ッキした場合でも、接着界面pn接合面ともに前記と同
様な結果が得られ、拡散深さの測定値も一致した。この
他、硫酸、硝酸、酢酸、沸化アンモニウムを用いた場合
でも同じ結果を示した。Note that even when the polished pellets were immersed in boiling acid for 5 seconds and then copper plated, the same results as above were obtained for both the adhesion interface and the pn junction surface, and the measured values of the diffusion depth also matched. In addition, the same results were obtained when sulfuric acid, nitric acid, acetic acid, and ammonium fluoride were used.
第2の実施例
直径76av+、厚さ0.50mm、 N型、面方位(
ioo) 。Second example diameter 76av+, thickness 0.50mm, N type, surface orientation (
ioo).
比抵抗0.01Ω・am(Pドープ)のシリコンウェハ
と直径、厚さが同じP型、面方位(100)、比抵抗2
8Ω・cm(Bドープ)のシリコンウェハを用いた。P-type with the same diameter and thickness as a silicon wafer with a resistivity of 0.01Ω・am (P-doped), surface orientation (100), and resistivity 2
A silicon wafer of 8 Ω·cm (B doped) was used.
二枚のウェハを第1の実施例と同様な洗浄処理、乾燥後
、同じ方法で接着、熱処理して接着シリコンウェハを作
成した。このウェハから第1の実施例と同様方法で研磨
ペレットを作成した。このペレットを少量の沸酸が添加
されている硫酸銅飽和溶液に30秒間浸漬させながら、
白熱電球で照らして、銅メッキ膜を析出させ、水洗後、
乾燥した。Two wafers were cleaned and dried in the same manner as in the first example, and then bonded and heat treated in the same manner to produce bonded silicon wafers. Polished pellets were made from this wafer in the same manner as in the first example. The pellets were immersed for 30 seconds in a saturated copper sulfate solution to which a small amount of boiling acid had been added.
The copper plating film is deposited by illuminating it with an incandescent light bulb, and after washing with water,
Dry.
二のペレットの接着界面を顕微鏡で調べたが、接着界面
は検出できず、pn接合面は不明瞭であった。しかし、
同様に作成したペレットを10重量%水酸化ナトリウム
溶液に5秒間、浸漬させてがら、前記と同様に硫酸銅飽
和溶液に30秒間浸漬させながら、ランプで照らして、
銅メッキ膜を析出させ。The adhesive interface of the second pellet was examined using a microscope, but no adhesive interface could be detected and the pn junction surface was unclear. but,
Pellets prepared in the same manner were immersed in a 10% by weight sodium hydroxide solution for 5 seconds, and immersed in a saturated copper sulfate solution for 30 seconds in the same manner as above, while being illuminated with a lamp.
Deposit a copper plating film.
水洗後、乾燥した。このペレットの接着界面を顕微鏡で
調べると、接着界面及びpn接合面ともに明瞭に検出す
ることができた。不純物の拡散深さの測定値は計算値と
1p以内の精度で一致した。After washing with water, it was dried. When the adhesive interface of this pellet was examined using a microscope, both the adhesive interface and the pn junction surface could be clearly detected. The measured value of the impurity diffusion depth agreed with the calculated value with an accuracy of within 1 p.
尚、研磨したペレットを5重量%の水酸化カリウム溶液
に20秒間浸漬してから、銅メッキした場合でも、接着
界面pn接合面ともに前記と同様な結果が得られ、拡散
深さの測定値も一致した。In addition, even when the polished pellet was immersed in a 5% by weight potassium hydroxide solution for 20 seconds and then plated with copper, the same results as above were obtained for both the adhesive interface pn junction surface, and the measured value of the diffusion depth was also Agreed.
以上のように本発明を用いれば、従来法では不可能だっ
た接着シリコンウェハの不純物の拡散深さを簡便で精度
良く測定できることがら、直接接着技術を用いた半導体
デバイス製造プロセスに応用すれば、デバイスの製造技
術及び品質管理などの半導体産業に大きく寄与する。As described above, if the present invention is used, it is possible to easily and precisely measure the diffusion depth of impurities in a bonded silicon wafer, which was impossible with conventional methods.If applied to a semiconductor device manufacturing process using direct bonding technology, It will greatly contribute to the semiconductor industry in terms of device manufacturing technology and quality control.
代理人 弁理士 則 近 憲 佑 同 竹 花 喜久男Agent: Patent Attorney Noriyuki Chika Same Bamboo Flower Kikuo
Claims (1)
異物を含まない清浄雰囲気下で接触させ、熱処理として
一体化させる直接接着法により作成した半導体基板を、
光照射下の硫酸銅溶液中で銅メッキする際、酸またはア
ルカリ溶液に浸漬後、銅メッキすることを特徴とする半
導体基板のメッキ法。Semiconductor substrates are manufactured using a direct bonding method in which the mirror surfaces of two mirror-polished semiconductor substrates are brought into contact with each other in a clean atmosphere that is substantially free of foreign matter, and then integrated through heat treatment.
A plating method for a semiconductor substrate, which is characterized in that when copper plating is performed in a copper sulfate solution under light irradiation, copper plating is performed after immersion in an acid or alkaline solution.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3806287A JPS63205908A (en) | 1987-02-23 | 1987-02-23 | Plating method for semiconductor substrate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3806287A JPS63205908A (en) | 1987-02-23 | 1987-02-23 | Plating method for semiconductor substrate |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63205908A true JPS63205908A (en) | 1988-08-25 |
Family
ID=12515009
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3806287A Pending JPS63205908A (en) | 1987-02-23 | 1987-02-23 | Plating method for semiconductor substrate |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63205908A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6027949A (en) * | 1997-01-07 | 2000-02-22 | Mitsubishi Denki Kabushiki Kaisha | Method for evaluating a semiconductor device |
-
1987
- 1987-02-23 JP JP3806287A patent/JPS63205908A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6027949A (en) * | 1997-01-07 | 2000-02-22 | Mitsubishi Denki Kabushiki Kaisha | Method for evaluating a semiconductor device |
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