JPH0867974A - Sputtering target for forming thin platinum film - Google Patents

Sputtering target for forming thin platinum film

Info

Publication number
JPH0867974A
JPH0867974A JP22570294A JP22570294A JPH0867974A JP H0867974 A JPH0867974 A JP H0867974A JP 22570294 A JP22570294 A JP 22570294A JP 22570294 A JP22570294 A JP 22570294A JP H0867974 A JPH0867974 A JP H0867974A
Authority
JP
Japan
Prior art keywords
thin film
thickness
target
sputtering target
sputtering
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP22570294A
Other languages
Japanese (ja)
Other versions
JP3246223B2 (en
Inventor
Akira Mori
暁 森
Naoki Uchiyama
直樹 内山
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Materials Corp
Original Assignee
Mitsubishi Materials Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Mitsubishi Materials Corp filed Critical Mitsubishi Materials Corp
Priority to JP22570294A priority Critical patent/JP3246223B2/en
Publication of JPH0867974A publication Critical patent/JPH0867974A/en
Application granted granted Critical
Publication of JP3246223B2 publication Critical patent/JP3246223B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE: To provide a sputtering target uniform in thickness and radiating a small amt. of α-particles. CONSTITUTION: This sputtering target contains 0.5-5ppm, in total, of one or more among Fe, Ni and Co and <=5ppb, in total, of U, Th and radioactive isotopes mainly including decayed nuclides of U and Th in Pt of >=99.999wt.% purity. When this target is used, a thin Pt film not causing a soft error due to α-rays can be formed.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】この発明は、半導体メモリーなど
のキャパシタ薄膜表面に電極としてのPt薄膜を形成す
るためのスパッタリングターゲットに関するものであ
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a sputtering target for forming a Pt thin film as an electrode on the surface of a capacitor thin film such as a semiconductor memory.

【0002】[0002]

【従来の技術】最近、64MDRMなど半導体メモリー
などにおいて、ペロブスカイト構造を有するBaTi複
合酸化物薄膜、SrTi複合酸化物薄膜、BaSrTi
複合酸化物薄膜を半導体メモリーなどのキャパシタ薄膜
として使用する研究が進んでいる。
2. Description of the Related Art Recently, in a semiconductor memory such as 64 MDRM, a BaTi complex oxide thin film having a perovskite structure, a SrTi complex oxide thin film, and a BaSrTi thin film.
Research is underway to use composite oxide thin films as capacitor thin films for semiconductor memories and the like.

【0003】前記ペロブスカイト構造を有するBaTi
複合酸化物薄膜、SrTi複合酸化物薄膜、BaSrT
i複合酸化物薄膜を半導体メモリーのキャパシタとして
使用する場合に、キャパシタの電極として99.99%
〜99.999%の高純度のPt薄膜が使用される。こ
の高純度Pt薄膜は、高純度Ptターゲットを用いてス
パッタリングすることにより形成される。
BaTi having the perovskite structure
Complex oxide thin film, SrTi complex oxide thin film, BaSrT
When the i-composite oxide thin film is used as a capacitor for semiconductor memory, it is used as a capacitor electrode at 99.99%.
A high purity Pt thin film of ˜99.999% is used. This high-purity Pt thin film is formed by sputtering using a high-purity Pt target.

【0004】[0004]

【発明が解決しようとする課題】Ptは、価格が高価で
あるためにPt薄膜は、可及的に薄くしたいという要望
があり、厚さ:1000オングストローム以下にしたい
という要望がある。しかし、従来の高純度Ptターゲッ
トを用いてスパッタリングにより厚さ:1000オング
ストローム以下のPt薄膜を形成すると膜厚が不均一に
なり、キャパシタの電極としては満足のいくものではな
かった。
Since Pt is expensive, there is a demand for the Pt thin film to be as thin as possible, and there is a demand for the Pt thin film to have a thickness of 1000 angstroms or less. However, when a Pt thin film having a thickness of 1000 angstroms or less is formed by sputtering using a conventional high-purity Pt target, the film thickness becomes nonuniform, which is not satisfactory as a capacitor electrode.

【0005】さらに、通常のPtにはU、Th並びにこ
れら崩壊核種を主体とする放射性同位元素を50ppb
以上含まれており、この通常のPtターゲットにより得
られたPt薄膜をキャパシタの電極とすると、Pt薄膜
から放出されるα線がキャパシタに影響を与え、α線に
よるソフトエラーのために特に64Mや256M以上の
DRAMでの使用が不可能であった。
Further, normal Pt contains 50 ppb of U, Th and radioisotopes mainly composed of these decay nuclides.
If the Pt thin film obtained by this ordinary Pt target is used as the electrode of the capacitor, the α rays emitted from the Pt thin film affect the capacitor, and 64 M or It could not be used in a DRAM of 256M or more.

【0006】[0006]

【課題を解決するための手段】そこで、本発明者らは、
厚さ:1000オングストローム以下のPt薄膜を形成
しても膜厚が均一でかつα線によるソフトエラーのない
Pt薄膜を得ることのできるPtターゲットを開発すべ
く研究を行なった結果、Fe、Ni、Coの内の1種ま
たは2種以上を合計で0.5〜5ppmを含有し、かつ
UおよびTh、並びにこれら崩壊核種を主体とする放射
性同位元素の含有量を5ppb以下にしたPtターゲッ
トを用いてスパッタリングすると、膜厚が均一でかつα
線によるソフトエラーのないPt薄膜が得られる、とい
う知見を得たのである。
Therefore, the present inventors have
Thickness: Even if a Pt thin film having a thickness of 1000 angstroms or less is formed, research was conducted to develop a Pt target that can obtain a Pt thin film having a uniform film thickness and free of soft error due to α rays. As a result, Fe, Ni, A Pt target containing 0.5 to 5 ppm in total of one or more of Co and 0.5 to 5 ppm in total, and U and Th, and the content of radioisotopes mainly containing these decay nuclides to 5 ppb or less is used. When sputtering, the film thickness is uniform and α
We have found that a Pt thin film can be obtained without soft errors due to lines.

【0007】この発明は、かかる知見に基づいて成され
たものであって、Fe、Ni、Coの内の1種または2
種以上を合計で0.5〜5ppmを含有し、かつUおよ
びTh、並びにこれら崩壊核種を主体とする放射性同位
元素の含有量が5ppb以下である純度:99.999
重量%以上のPtからなるPt薄膜形成用スパッタリン
グターゲットに特徴を有するものである。
The present invention has been made on the basis of such findings, and is one of Fe, Ni and Co or two of Fe, Ni and Co.
Purity: 99.999 containing 0.5 to 5 ppm in total of 5 or more species and having a radioisotope content of 5 or less and U and Th and mainly these decay nuclides.
It is characterized by a sputtering target for forming a Pt thin film, which is composed of Pt in an amount of at least wt%.

【0008】この発明のPt薄膜形成用スパッタリング
ターゲットに含まれるFe、Ni、Coの内の1種また
は2種以上の合計を0.5〜5ppmに限定したのは、
これら金属が0.5ppm未満だと、スパッタリングし
て得られた厚さ:1000オングストローム以下のPt
薄膜の厚さのばらつきが大きくなるので好ましくなく、
一方、5ppmを越えて含有してもPt薄膜の厚さのば
らつきが大きくなるので好ましくないことによるもので
ある。
In the sputtering target for forming a Pt thin film of the present invention, the total content of one or more of Fe, Ni and Co is limited to 0.5 to 5 ppm.
If these metals are less than 0.5 ppm, the thickness obtained by sputtering: Pt of 1000 angstroms or less
It is not preferable because the variation in the thickness of the thin film becomes large,
On the other hand, even if the content exceeds 5 ppm, the variation in the thickness of the Pt thin film becomes large, which is not preferable.

【0009】また、この発明のPt薄膜形成用スパッタ
リングターゲットに含まれるUおよびTh、並びにこれ
ら崩壊核種を主体とする放射性同位元素の含有量が5p
pb以下としたのは、5ppb以下であればα線の放出
量が0.001CPH/cm2 以下となってα線による
ソフトエラーが無視できるからである。
Further, the contents of U and Th contained in the sputtering target for forming a Pt thin film of the present invention and the content of radioisotopes mainly containing these decay nuclides are 5 p.
The reason for setting it to pb or less is that if it is 5 ppb or less, the emission amount of α rays becomes 0.001 CPH / cm 2 or less, and the soft error due to α rays can be ignored.

【0010】[0010]

【実施例】【Example】

市販の純度:99.9重量%、厚さ:1mmのPt板を
縦:5cm、横:20cmの寸法に切断し、これを陽極
電極として下記の条件、 溶融塩組成:NaCl:24.3%、LiCl:39.
2%、KCl:36.5%、 溶融塩温度:500℃±10℃、 電圧 :0.1V、 電流 :5A、 で溶融塩電解を3回繰り返して精製し、Ptの純度を表
1〜表2に示される値に高め、UおよびTh、並びにこ
れら崩壊核種を主体とする放射性同位元素の含有量を表
1〜表2に示される値に低減した。
A commercially available Pt plate having a purity of 99.9% by weight and a thickness of 1 mm was cut into a size of length: 5 cm, width: 20 cm, and this was used as an anode electrode under the following conditions: Molten salt composition: NaCl: 24.3% , LiCl: 39.
2%, KCl: 36.5%, molten salt temperature: 500 ° C. ± 10 ° C., voltage: 0.1 V, current: 5 A, molten salt electrolysis was repeated 3 times for purification, and the purity of Pt was shown in Tables 1 to 1. 2, the contents of U and Th, and radioisotopes mainly containing these decay nuclides were reduced to the values shown in Tables 1 and 2.

【0011】このUおよびTh、並びにこれら崩壊核種
を主体とする放射性同位元素の含有量の少ない高純度P
tをさらに真空溶解し、Fe、Ni、Coの内の1種ま
たは2種以上を微量添加したのち、直径:100mm、
厚さ:20mmの鋳塊を作り、この鋳塊を熱間圧延して
厚さ:6mmにし、これを機械加工して、直径:100
mm、厚さ:6mmの円板に仕上げ、本発明Pt薄膜形
成用スパッタリングターゲット(以下、本発明Ptター
ゲットという)1〜13を作製した。
High purity P containing U and Th, and radioisotopes mainly containing these decay nuclides and having a small content.
After further melting t in vacuum and adding a trace amount of one or more of Fe, Ni and Co, a diameter: 100 mm,
A slab with a thickness of 20 mm was made, and this slab was hot-rolled to a thickness of 6 mm, which was machined to a diameter of 100.
mm, thickness: 6 mm, and finished into a circular plate having a thickness of 6 mm to prepare sputtering targets 1 to 13 for forming a Pt thin film of the present invention (hereinafter referred to as Pt target of the present invention).

【0012】一方、比較のために、実施例1で帯溶融精
製し、UおよびTh、並びにこれら崩壊核種を主体とす
る放射性同位元素の含有量を低減した高純度Ptに、F
e、Ni、Coの内の1種または2種以上を0.5〜5
ppmの範囲外となるように添加しまたは添加すること
なく比較Pt薄膜形成用スパッタリングターゲット(以
下、比較Ptターゲットという)1〜6を作製し、さら
に通常の高純度Ptからなる従来Pt薄膜形成用スパッ
タリングターゲット(以下、従来Ptターゲットとい
う)を作製した。
On the other hand, for comparison, in Example 1, high-purity Pt which had been zone-melted and refined to reduce the contents of U and Th, and radioisotopes mainly containing these decay nuclides, was used.
One or more of e, Ni, and Co is 0.5 to 5
Sputtering targets for comparative Pt thin film formation (hereinafter referred to as comparative Pt targets) 1 to 6 were prepared with or without addition so as to fall outside the range of ppm, and for conventional Pt thin film formation consisting of ordinary high-purity Pt A sputtering target (hereinafter referred to as a conventional Pt target) was produced.

【0013】これら本発明Ptターゲット1〜13、比
較Ptターゲット1〜6および従来Ptターゲットを無
酸素銅製冷却板にIn−Sn共晶はんだを用いてはんだ
付けしたのち、通常の高周波マグネトロンスパッタ装置
に取り付け、直径:100mm、厚さ:0.5mmのS
i板に下記の条件、 雰囲気ガス:Ar、 雰囲気圧力:1pa、 Si板表面温度:500℃、 ターゲットとSi板の距離:5cm、 にてスパッタを行い、高周波マグネトロンスパッタ装置
内にセットした直径:100mmのSi板の上に表3〜
表4に示される目標Pt膜厚となるようにPt薄膜を形
成し、Si板の中央部表面に形成された現実の最高Pt
膜厚および最低Pt膜厚を求め、その結果を表3〜表4
に示した。
These Pt targets 1 to 13 of the present invention, comparative Pt targets 1 to 6 and conventional Pt targets were soldered to an oxygen-free copper cooling plate using an In-Sn eutectic solder, and then used in a normal high frequency magnetron sputtering apparatus. Mounting, diameter: 100 mm, thickness: 0.5 mm S
Sputtering was performed on the i plate under the following conditions: atmosphere gas: Ar, atmosphere pressure: 1 pa, Si plate surface temperature: 500 ° C., distance between target and Si plate: 5 cm, and diameter set in high frequency magnetron sputtering device: Table 3 ~ on a 100 mm Si plate
The actual maximum Pt formed on the surface of the central portion of the Si plate by forming a Pt thin film so as to have the target Pt film thickness shown in Table 4
The film thickness and the minimum Pt film thickness were obtained, and the results are shown in Tables 3 to 4.
It was shown to.

【0014】さらに、ガスフロー比例計数管を用い、本
発明Ptターゲット1〜13、比較Ptターゲット1〜
6および従来Ptターゲットのα線粒子のカウント数を
測定し、それらの結果を表3〜表4に示した。
Further, by using a gas flow proportional counter, the Pt targets 1 to 13 of the present invention and the comparative Pt targets 1 to 1 are used.
6 and conventional Pt target α-ray particle counts were measured and the results are shown in Tables 3-4.

【0015】[0015]

【表1】 [Table 1]

【0016】[0016]

【表2】 [Table 2]

【0017】[0017]

【表3】 [Table 3]

【0018】[0018]

【表4】 [Table 4]

【0019】[0019]

【発明の効果】表1〜表4に示される結果から、Fe、
Ni、Coの内の1種または2種以上を合計で0.5〜
5ppm含有しかつUおよびTh並びにこれら崩壊核種
を主体とする放射性同位元素の含有量を5ppb以下を
含有する本発明Ptターゲット1〜13により形成され
た最高Pt膜厚と最低Pt膜厚の差は、従来Ptターゲット
により形成された最高Pt膜厚と最低Pt膜厚の差に比べて
極めて小さく、また本発明Ptターゲット1〜13によ
り放射されるα粒子の放射量が従来Ptターゲットによ
り放射されるα粒子の放射量に比べて極めて少ないとこ
ろから、本発明Ptターゲット1〜13により形成され
たPt薄膜の厚さは従来Ptターゲットにより形成され
たPt薄膜の厚さに比べて均一でありかつα粒子の放射
量が極めて少ないことが分かる。
From the results shown in Tables 1 to 4, Fe,
One or two or more of Ni and Co in total of 0.5 to
The difference between the highest Pt film thickness and the lowest Pt film thickness formed by the Pt targets 1 to 13 of the present invention containing 5 ppm and U and Th and the content of radioisotopes mainly containing these decay nuclides is 5 ppb or less. In comparison with the difference between the maximum Pt film thickness and the minimum Pt film thickness formed by the conventional Pt target, the amount of α particles emitted by the Pt targets 1 to 13 of the present invention is emitted by the conventional Pt target. Since the amount of radiation of the α particles is extremely small, the thickness of the Pt thin film formed by the Pt targets 1 to 13 of the present invention is more uniform than that of the Pt target formed by the conventional Pt target, and α It can be seen that the radiation dose of the particles is extremely low.

【0020】しかし、この発明の条件から外れてFe、
Ni、Coの内の1種または2種以上を合計で含有する
比較Ptターゲット1〜6(表2において*印を付して
示した)は、Pt薄膜の厚さが不均一となることも分か
る。
However, if Fe is out of the condition of the present invention,
Comparative Pt targets 1 to 6 (shown with an asterisk in Table 2) containing one or more of Ni and Co in total may have a non-uniform Pt thin film thickness. I understand.

【0021】したがって、この発明のPtスパッタリン
グターゲットを用いると、従来のPtスパッタリングタ
ーゲットよりも膜厚が均一でα線放射の少ないPt薄膜
を得ることのでき、半導体メモリーのキャパシタの電極
として優れかつソフトエラーのない半導体メモリーを提
供することができるなど産業上優れた効果を奏するもの
である。
Therefore, when the Pt sputtering target of the present invention is used, a Pt thin film having a more uniform film thickness and less α-ray emission than the conventional Pt sputtering target can be obtained, which is excellent as a capacitor electrode of a semiconductor memory and is soft. This is an industrially excellent effect such that an error-free semiconductor memory can be provided.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 Fe、Ni、Coの内の1種または2種
以上を合計で0.5〜5ppmを含有し、かつUおよび
Th、並びにこれら崩壊核種を主体とする放射性同位元
素の含有量を5ppb以下にした純度:99.999重
量%以上のPtからなることを特徴とするPt薄膜形成
用スパッタリングターゲット。
1. A radioisotope content containing 0.5 to 5 ppm in total of one or more of Fe, Ni, and Co, and U and Th, and mainly these decay nuclides. The sputtering target for Pt thin film formation is characterized by comprising Pt in an amount of 99.999% by weight or more with a purity of 5 ppb or less.
JP22570294A 1994-08-26 1994-08-26 Sputtering target for Pt thin film formation Expired - Fee Related JP3246223B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22570294A JP3246223B2 (en) 1994-08-26 1994-08-26 Sputtering target for Pt thin film formation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22570294A JP3246223B2 (en) 1994-08-26 1994-08-26 Sputtering target for Pt thin film formation

Publications (2)

Publication Number Publication Date
JPH0867974A true JPH0867974A (en) 1996-03-12
JP3246223B2 JP3246223B2 (en) 2002-01-15

Family

ID=16833466

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22570294A Expired - Fee Related JP3246223B2 (en) 1994-08-26 1994-08-26 Sputtering target for Pt thin film formation

Country Status (1)

Country Link
JP (1) JP3246223B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999066099A1 (en) * 1998-06-17 1999-12-23 Tanaka Kikinzoku Kogyo K.K. Target material for spattering
US6875324B2 (en) 1998-06-17 2005-04-05 Tanaka Kikinzoku Kogyo K.K. Sputtering target material
JP2006161066A (en) * 2004-12-02 2006-06-22 Seiko Epson Corp Sputtering target, manufacturing method therefor, sputtering device and liquid-spouting head
WO2009119196A1 (en) * 2008-03-28 2009-10-01 日鉱金属株式会社 Platinum powder for magnetic material target, method for producing the powder, method for producing magnetic material target composed of platinum sintered compact, and the sintered magnetic material target

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999066099A1 (en) * 1998-06-17 1999-12-23 Tanaka Kikinzoku Kogyo K.K. Target material for spattering
GB2343684A (en) * 1998-06-17 2000-05-17 Tanaka Precious Metal Ind Target material for spattering
GB2343684B (en) * 1998-06-17 2003-04-23 Tanaka Precious Metal Ind Sputtering target material
US6875324B2 (en) 1998-06-17 2005-04-05 Tanaka Kikinzoku Kogyo K.K. Sputtering target material
JP2006161066A (en) * 2004-12-02 2006-06-22 Seiko Epson Corp Sputtering target, manufacturing method therefor, sputtering device and liquid-spouting head
WO2009119196A1 (en) * 2008-03-28 2009-10-01 日鉱金属株式会社 Platinum powder for magnetic material target, method for producing the powder, method for producing magnetic material target composed of platinum sintered compact, and the sintered magnetic material target
JP5301530B2 (en) * 2008-03-28 2013-09-25 Jx日鉱日石金属株式会社 Platinum powder for magnetic material target, method for producing the same, method for producing magnetic material target comprising a platinum sintered body, and the same sintered magnetic material target

Also Published As

Publication number Publication date
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