JP4585129B2 - Electrostatic chuck - Google Patents
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- JP4585129B2 JP4585129B2 JP2001038132A JP2001038132A JP4585129B2 JP 4585129 B2 JP4585129 B2 JP 4585129B2 JP 2001038132 A JP2001038132 A JP 2001038132A JP 2001038132 A JP2001038132 A JP 2001038132A JP 4585129 B2 JP4585129 B2 JP 4585129B2
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Description
【0001】
【発明の属する技術分野】
本発明は、半導体製造装置等において、シリコンウェハ等の被吸着物を固定、搬送、矯正するために用いられる静電チャックに関する。
【0002】
【従来の技術】
電極とその上面に誘電体層が設けられている静電チャックにおいて、その誘電体層としては、従来、アルミナ、サファイア等の絶縁性のセラミックスが用いられている。
【0003】
【発明が解決しようとする課題】
しかしながら、これら絶縁性のセラミックスでは、電極に誘起される電荷と静電チャックに吸着すべき被吸着体に誘起される電荷との間に発生する静電吸着力(クーロン力)で吸着することから、高い吸着力を得るためには、誘電体層の厚さを0.1mm以下と薄くしなければならないという問題があった。
【0004】
本発明は、上述した静電チャックが有する課題に鑑みなされたものであって、その目的は、誘電体層の厚さに関係なく吸着できる誘電体層を有する静電チャックを提供することにある。
【0005】
【課題を解決するための手段】
本発明者等は、上記目的を達成するため鋭意研究した結果、誘電体層の材質をTiO2-xまたはCr2O3-xを含むスピネル質焼結体とすれば、誘電体層の厚さに関係なく吸着できる誘電体層を有する静電チャックが得られるとの知見を得て本発明を完成するに至った。
【0006】
即ち本発明は、
(1)電極の上面に誘電体層が設けられた静電チャックにおいて、該誘電体層が、主成分がMgOとAl2O3からなり、その組成比がMgO/Al2O3の重量比で0.67〜2.33の範囲にあり、その主成分にTiO2-xを3〜30重量%含むスピネル質焼結体からなり、かつその電気伝導率が、10-8〜10-14S/cmであることを特徴とする静電チャック(請求項1)とし、
(2)電極の上面に誘電体層が設けられた静電チャックにおいて、該誘電体層が、主成分がMgOとAl2O3からなり、その組成比がMgO/Al2O3の重量比で0.67〜2.33の範囲にあり、その主成分にCr2O3-xを3〜30重量%含むスピネル質焼結体からなり、かつその電気伝導率が、10-8〜10-14S/cmであることを特徴とする静電チャック(請求項2)とし、
(3)前記スピネル質焼結体の腐食ガスに対する耐食性が、ハロゲン系プラズマガス対するエッチングレートで、5μm/hr以下であることを特徴とする請求項1または2記載の静電チャック(請求項3)とし、
(4)前記スピネル質焼結体が、MgO粉末、Al2O3粉末、TiO2粉末とを請求項1記載の組成となるよう配合し、それを混合し、成形し、その成形した成形体を還元雰囲気中で焼結することにより作製された焼結体であることを特徴とする請求項1または3記載の静電チャック(請求項4)とし、
(5)前記スピネル質焼結体が、MgO粉末、Al2O3粉末、Cr2O3粉末とを請求項2記載の組成となるよう配合し、それを混合し、成形し、その成形した成形体を還元雰囲気中で焼結することにより作製されと焼結体であることを特徴とする請求項2または3記載の静電チャック(請求項5)とし、
(6)前記スピネル質焼結体が、MgO粉末、Al2O3粉末、TiO2粉末とを請求項1記載の組成となるよう配合し、それを混合し、成形し、その成形した成形体を空気中で焼結した後、それをさらに還元雰囲気中で加熱処理することにより作製された焼結体であることを特徴とする請求項1または3記載の静電チャック(請求項6)とし、
(7)前記スピネル質焼結体が、MgO粉末、Al2O3粉末、Cr2O3粉末とを請求項2記載の組成となるよう配合し、それを混合し、成形し、その成形した成形体を空気中で焼結した後、それをさらに還元雰囲気中で加熱処理することにより作製された焼結体であることを特徴とする請求項2または3記載の静電チャック(請求項7)とすることを要旨とする。
以下さらに詳細に説明する。
【0007】
上記で述べたように、本発明の静電チャックとしては、ウェハを吸着する誘電体層を主成分がMgOとAl2O3からなり、そのMgO/Al2O3比が重量比で0.67〜2.33の範囲にあり、その主成分にTiO2-xまたはCr2O3-xを3〜30重量%含むスピネル質焼結体からなり、かつその電気伝導率が、10-8〜10-14S/cmであることとする静電チャックとした(請求項1、2)
【0008】
静電チャックとして、その誘電体層の材質をTiO2-xまたはCr2O3-xを含むスピネル質焼結体としたのは、導電性のあるTiO2-xまたはCr2O3-xを含ませることにより、誘電体層に導電性を持たせ、その導電性によりジョンセン・ラーベック力を発現させ、誘電体層の厚さに関係なく吸着できる誘電体層となり、加えてスピネルを母体とすることにより、ハロゲン系プラズマガスに優れた耐食性を有する誘電体層となることによる。
【0009】
そのスピネル質焼結体のMgO/Al2O3の比としては、0.67〜2、33が好ましく、その比が0.67より小さいと焼結体の強度が大きく低下して好ましくなく、2.33より高くてもやはり焼結体の強度が大きく低下して好ましくない。
【0010】
そのスピネル質焼結体のTiO2-xまたはCr2O3-xの含有率としては、3〜30重量%が好ましく、3重量%より少ないと電気伝導率が10-14S/cm以上とならないので好ましくなく、30重量%より多いと10-8S/cm以下とならないので好ましくない。
【0011】
そして、そのスピネル質焼結体の電気伝導率としては、10-8〜10-14S/cmの範囲の電気伝導率がジョンセン・ラーベック力が有効に働くため好ましく、電気伝導率が10-8S/cmより高いと吸着したウェハにリーク電流が流れてウェハに形成されている回路が破壊される恐れがあり、10-14S/cmより低いとジョンセン・ラーベック力が有効に働かず高い吸着力が得られない。このような範囲の電気伝導率は、少なくとも−50〜200℃の範囲で得られていればよい。
【0012】
一方、そのスピネル質焼結体の耐食性の度合いとしては、ハロゲン系プラズマガスに対するエッチングレートで、5μm/hr以下になるとした(請求項3)。このスピネル質焼結体がTiO2-xまたはCr2O3-xを含んでもこのような優れた耐食性を有するのは、恐らくTiO2-xまたはCr2O3-xがスピネル結晶格子中に固溶するためか、あるいはMgTiO3-x、MgTi2O5-x、MgCr2O4-xなどの複合酸化物を生成するためではないかと思われる。これにより極めて耐食性に強い誘電体層となる。
【0013】
そのスピネル質焼結体の作製方法としては、所定の組成となるよう配合し、それを混合し、成形し、その成形した成形体を還元雰囲気中で焼結することにより作製されることとした(請求項4、5)。TiO2またはCr2O3は、酸素欠損が生じないと導電性を有しないので、それを還元雰囲気中で焼結することにより、酸素欠損を生じさせるものである。
【0014】
また、別の作製方法としては、所定の組成となるよう配合し、それを混合し、成形し、その成形した成形体を空気中で焼結した後、さらに還元雰囲気中で加熱処理することにより作製されることとした(請求項6、7)。これは、一旦、酸素欠損のない焼結体を作製し、その焼結体を還元雰囲気中で加熱処理するものであり、この方法でも同じように酸素欠損を生じさせるものである。
【0015】
【発明の実施の形態】
静電チャックの作製について述べると、先ずスピネル質焼結体を作製するためにMgO粉末、Al2O3粉末、TiO2粉末を、またはMgO粉末、Al2O3粉末、Cr2O3粉末を所定の配合に調合する。前記した粉末の代わりに例えばMgOとAl2O3を含むMAl2O4などの複合酸化物を用いてもよい。これら粉末の調合は、従来法に準じて調製すればよい。例えば先に述べた粉末を所定の割合で配合し、その配合粉末にアルコール等の有機溶媒または水を加え、ボールミルで混合後、乾燥する方法、あるいは所定の配合の塩類、アルコキシド等の溶液から共沈物を分離し乾燥する方法等がある。
【0016】
得られた混合粉末を一軸プレスまたは冷間静水圧プレス(CIP)等によって所定形状に成形する。得られた成形体を還元雰囲気中で所定の温度で焼結することにより、あるいは得られた成形体を大気中で所定の温度で焼結し、これをさらに還元雰囲気中で所定の温度で加熱処理することにより、導電性を有するスピネル質焼結体が作製される。酸素を欠損させる度合いは、還元雰囲気中の還元力によって異なるが、通常使用されるカーボン雰囲気程度の還元力では、TiO2またはCr2O3の酸素のみが欠損されるだけで、スピネル中の酸素をも欠損させることはない。
【0017】
その焼結体を焼結する温度としては、1500〜1650℃が好ましく、1500℃より低いと緻密化が不十分となり、1650℃より高いと焼結体が分解する恐れがある。その焼結した焼結体をさらに加熱処理する温度としては、焼結する温度と同じでよいが、熱間静水圧処理(HIP処理)する場合には、1400〜1650℃が好ましく、1400℃より低い、または1650℃より高いとHIP処理の効果が少なく、その時の圧力としては1800kg/cm2より低いとこれもHIP処理の効果が少ない。
【0018】
得られたスピネル質焼結体に含まれるSiO2、CaO、Na2O、Fe2O3等の不純物成分としては、3重量%以下が好ましく、3重量%より多いと、例えば、半導体製造装置の装置内で絶縁不良を起こすなどの問題が生じるので好ましくない。また、得られたスピネル質焼結体の気孔率としては、1%以下が好ましく、気孔率が1%を越えると焼結体中に気孔が多く存在するため、表面を加工するとその気孔が表面に現れ、その気孔の部分でハロゲン系プラズマガスの腐食反応が激しく起こり、表面が著しく腐食されるため好ましくない。
【0019】
次いで、得られたスピネル質焼結体を加工などして誘電体層を作製し、その誘電体層を電極を形成したセラミックス基体の上面に接着して、あるいは得られた誘電体層を電極の上面に接着して、もしくは誘電体層の下面に電極を形成して単極型または双極型の静電チャックを作製する。なお、上記は誘電体層を焼結で作製しているが、このほかセラミックス、金属などの基体表面に溶射やスパッタ等により成膜し、それを還元雰囲気中で還元処理したものであってもよい。
【0020】
以上述べた方法で静電チャックを作製すれば、導電性を有し、かつ耐食性を有する誘電体層が形成された静電チャックが得られる。
【0021】
【実施例】
以下、本発明の実施例を比較例と共に具体的に挙げ、本発明をより詳細に説明する。
【0022】
(実施例1〜7)
(1)静電チャックの作製
純度99%のMgAl2O4粉末と純度99.9%のMgO粉末をMgO/Al2O3の比が重量比で表1となるように調合し、それにTiO2またはCr2O3粉末をその添加率が表1となるよう添加し、それにエタノールを加え、それをボールミルで72時間混合粉砕した。
【0023】
それを乾燥した混合粉末をCIP処理してφ250×6mmtに成形し、その成形体を還元雰囲気中で1500〜1650℃の温度で焼結し(実施例1〜4)、あるいは成形体を大気中で1500〜1650℃の温度で焼結し、それにさらに還元雰囲気中で1400〜1650℃の温度で1800kg/cm2の圧力でHIP処理して(実施例5〜7)スピネル質焼結体を作製した。それら焼結体をφ200×2mmtに加工して誘電体層を作製した。
【0024】
得られた誘電体層の一方の面にAgペーストを印刷・焼き付けして電極を形成し、他方の面を表面粗さがRaで0.34μmとなるよう研磨し、その研磨面を表面をアノーダイジング(陽極酸化)したAl台座に接着剤で貼り付け静電チャックを作製した。
【0025】
(2)評価
得られたスピネル質焼結体の曲げ強度を3点曲げ試験法で測定した。また、得られた静電チャックの誘電体層の電気伝導率を直流3端子法で測定した。さらに、得られた静電チャックを平行平板電極型プラズマエッチング装置に組み込み、1kVの電荷を印加してシリコンウェハが吸着されるか否かを、シリコンウェハ上に形成されている回路が破壊されるか否かを調べた。さらにまた、周波数が2.45GHzで、出力が800Wで、CF4とO2の体積比が4:1のプラズマガスを吸着面に40分間エッチングし、そのエッチング後の誘電体層のエッチングレートを誘電体層の減少した重量で算出した。それらの結果を表1に示す。
【0026】
(比較例1〜7)
比較のために比較例1、2、5、6では、誘電体層のMgO/Al2O3の比を本発明の範囲外にした他は、比較例3、4では、TiO2の添加率を本発明の範囲外にした他は、また、比較例7では、誘電体層をアルミナとした他は実施例と同様に静電チャックを作製し、評価した。それらの結果も表1に示す。
【0027】
【表1】
【0028】
表1から明らかなように、誘電体層の電気伝導率は、実施例全てが本発明の範囲内にあった。そのため、シリコンウェハの吸着性が全て良好であった。また、ハロゲン系プラズマガスに対するエッチングレートが全て5μm/hr以下にあり、従前の比較例7のアルミナに比べてはるかによく、しかもTiO2の添加率が多くてもその添加率が少ない比較例3に比べて遜色なかった。このことは、本発明の静電チャックとすれば、誘電体層の厚さに関係なく吸着でき、しかも耐食性を有する誘電体層が形成された静電チャックとすることができることを示している。
【0029】
これに対して、比較例1、2、5、6では、MgO/Al2O3の比が本発明の範囲外にあるので、誘電体層の強度が低く、以後の評価を行わなかった。また、比較例3では、TiO2の添加率が低すぎたため、電気伝導率が低く、シリコンウェハを吸着できず、吸着性が悪かった。さらに、比較例4では、TiO2の添加率が多すぎたため、吸着性は良好なものの、電気伝導率が高すぎて回路がショートし回路破壊が生じてしまっており、しかもTiO2-xの単味のものが残存してしまったためか耐食性も悪かった。なお、比較例7では、耐食性が悪いばかりでなく、誘電体層が厚いため、吸着性が不良であった。
【0030】
【発明の効果】
以上の通り、本発明にかかる静電チャックであれば、導電性を有し、しかも耐食性の良好な誘電体層を有する静電チャックとすることができるようになった。
このことにより、誘電体層の厚さに関係なく吸着できる静電チャックとなり、しかもTiO2-xまたはCr2O3-xの含有率を調整することにより、必要とする電気伝導率に変えることのできる静電チャックともなるようになった。[0001]
BACKGROUND OF THE INVENTION
The present invention relates to an electrostatic chuck used for fixing, transporting, and correcting an object to be adsorbed such as a silicon wafer in a semiconductor manufacturing apparatus or the like.
[0002]
[Prior art]
In an electrostatic chuck in which an electrode and a dielectric layer are provided on an upper surface of the electrode, insulating ceramics such as alumina and sapphire are conventionally used as the dielectric layer.
[0003]
[Problems to be solved by the invention]
However, these insulating ceramics are attracted by the electrostatic attraction force (Coulomb force) generated between the charge induced on the electrode and the charge induced on the object to be adsorbed to the electrostatic chuck. In order to obtain a high attractive force, there has been a problem that the thickness of the dielectric layer must be reduced to 0.1 mm or less.
[0004]
The present invention has been made in view of the problems of the electrostatic chuck described above, and an object thereof is to provide an electrostatic chuck having a dielectric layer that can be adsorbed regardless of the thickness of the dielectric layer. .
[0005]
[Means for Solving the Problems]
As a result of diligent research to achieve the above object, the present inventors have determined that the thickness of the dielectric layer can be determined if the material of the dielectric layer is a spinel sintered body containing TiO 2-x or Cr 2 O 3-x. The present invention has been completed with the knowledge that an electrostatic chuck having a dielectric layer that can be adsorbed regardless of the thickness can be obtained.
[0006]
That is, the present invention
(1) In an electrostatic chuck in which a dielectric layer is provided on the upper surface of an electrode, the dielectric layer is mainly composed of MgO and Al 2 O 3 , and the composition ratio is the weight ratio of MgO / Al 2 O 3 . In the range of 0.67 to 2.33, and is composed of a spinel sintered body containing 3 to 30% by weight of TiO 2-x as a main component, and its electric conductivity is 10 −8 to 10 −14. S / cm is an electrostatic chuck (Claim 1),
(2) In an electrostatic chuck in which a dielectric layer is provided on the upper surface of the electrode, the dielectric layer is mainly composed of MgO and Al 2 O 3 , and the composition ratio is the weight ratio of MgO / Al 2 O 3 . In the range of 0.67 to 2.33, and is composed of a spinel sintered body containing 3 to 30% by weight of Cr 2 O 3-x as a main component and having an electric conductivity of 10 −8 to 10 -14 S / cm electrostatic chuck (claim 2),
(3) The electrostatic chuck according to claim 1 or 2, wherein the corrosion resistance of the spinel sintered body to a corrosive gas is 5 μm / hr or less at an etching rate with respect to a halogen-based plasma gas. )age,
(4) The spinel sintered body is composed of MgO powder, Al 2 O 3 powder, and TiO 2 powder so as to have the composition of claim 1, mixed and molded, and the molded body thus molded. The electrostatic chuck according to claim 1 or 3 (claim 4), wherein the electrostatic chuck is produced by sintering in a reducing atmosphere.
(5) The spinel sintered body is blended with MgO powder, Al 2 O 3 powder, and Cr 2 O 3 powder so as to have the composition of claim 2, mixed, molded, and molded. The electrostatic chuck according to claim 2 or 3 (claim 5), wherein the molded body is a sintered body produced by sintering in a reducing atmosphere.
(6) The spinel sintered body is composed of MgO powder, Al 2 O 3 powder, and TiO 2 powder so as to have the composition according to claim 1, mixed, molded, and molded body that is molded. The electrostatic chuck (Claim 6) according to claim 1 or 3, wherein the electrostatic chuck (Claim 6) is a sintered body produced by sintering in air and then heat-treating it in a reducing atmosphere. ,
(7) The spinel sintered body is composed of MgO powder, Al 2 O 3 powder, and Cr 2 O 3 powder so as to have the composition described in claim 2, mixed, molded, and molded. 4. The electrostatic chuck according to claim 2, which is a sintered body produced by sintering a molded body in air and then heat-treating the molded body in a reducing atmosphere. ).
This will be described in more detail below.
[0007]
As described above, in the electrostatic chuck of the present invention, the dielectric layer that adsorbs the wafer is mainly composed of MgO and Al 2 O 3 , and the MgO / Al 2 O 3 ratio is 0.00 by weight. It is in the range of 67 to 2.33, and is composed of a spinel sintered body containing 3 to 30% by weight of TiO 2-x or Cr 2 O 3-x as a main component, and has an electric conductivity of 10 −8. 10 to 14 −14 S / cm electrostatic chuck (claims 1 and 2)
[0008]
As the electrostatic chuck, the material of the dielectric layer is made of a spinel sintered body containing TiO 2-x or Cr 2 O 3-x , and the conductive TiO 2-x or Cr 2 O 3-x is used. The dielectric layer is made conductive, and the conductivity causes the Johnsen-Rahbek force to be generated, so that the dielectric layer can be adsorbed regardless of the thickness of the dielectric layer. By doing so, the dielectric layer has excellent corrosion resistance to the halogen-based plasma gas.
[0009]
The ratio of MgO / Al 2 O 3 of the spinel sintered body is preferably 0.67 to 2 and 33, and if the ratio is smaller than 0.67, the strength of the sintered body is greatly reduced, which is not preferable. Even if it is higher than 2.33, the strength of the sintered body is greatly lowered, which is not preferable.
[0010]
The content of TiO 2-x or Cr 2 O 3-x in the spinel sintered body is preferably 3 to 30% by weight, and if it is less than 3% by weight, the electric conductivity is 10 −14 S / cm or more. It is not preferable because it does not become, and if it exceeds 30% by weight, it is not preferable because it is not 10 −8 S / cm or less.
[0011]
As the electric conductivity of the spinel sintered body, an electric conductivity in the range of 10 −8 to 10 −14 S / cm is preferable because the Johnsen-Rahbek force works effectively, and the electric conductivity is 10 −8. S / cm and leakage current flows in the high and adsorbed wafer from there is a possibility that the circuit formed on the wafer is broken, 10 -14 S / cm lower than the Johnsen-Rahbek force is effectively exerted without high adsorption I can't get power. The electric conductivity of such a range should just be obtained in the range of -50-200 degreeC at least.
[0012]
On the other hand, the degree of corrosion resistance of the spinel sintered body is set to 5 μm / hr or less at an etching rate with respect to the halogen-based plasma gas. Even if this spinel sintered body contains TiO 2-x or Cr 2 O 3-x , this excellent corrosion resistance is probably because TiO 2-x or Cr 2 O 3-x is contained in the spinel crystal lattice. Probably because a solid solution, or MgTiO 3-x, MgTi 2 O 5-x, is believed that it is a to produce a composite oxide such as MgCr 2 O 4-x. As a result, the dielectric layer is extremely resistant to corrosion.
[0013]
As a method for producing the spinel sintered body, it is prepared by blending so as to have a predetermined composition, mixing, molding, and sintering the molded article in a reducing atmosphere. (Claims 4 and 5). TiO 2 or Cr 2 O 3 does not have electrical conductivity unless oxygen vacancies are generated, and therefore, oxygen vacancies are generated by sintering it in a reducing atmosphere.
[0014]
Further, as another production method, it is blended so as to have a predetermined composition, mixed, molded, sintered in the air, and further heat-treated in a reducing atmosphere. It was supposed to be produced (claims 6 and 7). In this method, a sintered body having no oxygen vacancies is once produced, and the sintered body is heat-treated in a reducing atmosphere. This method similarly causes oxygen vacancies.
[0015]
DETAILED DESCRIPTION OF THE INVENTION
Regarding production of an electrostatic chuck, first, MgO powder, Al 2 O 3 powder, TiO 2 powder, or MgO powder, Al 2 O 3 powder, Cr 2 O 3 powder are used to produce a spinel sintered body. Prepare to the prescribed recipe. A composite oxide such as MAl 2 O 4 containing MgO and Al 2 O 3 may be used instead of the above powder. What is necessary is just to prepare the preparation of these powders according to the conventional method. For example, the powder described above is blended at a predetermined ratio, and an organic solvent such as alcohol or water is added to the blended powder, followed by mixing with a ball mill and drying, or a solution of salts, alkoxide, or the like with a predetermined blend. There is a method of separating and drying the sediment.
[0016]
The obtained mixed powder is formed into a predetermined shape by a uniaxial press or a cold isostatic press (CIP). The obtained molded body is sintered at a predetermined temperature in a reducing atmosphere, or the obtained molded body is sintered at a predetermined temperature in the atmosphere and further heated at a predetermined temperature in a reducing atmosphere. By performing the treatment, a conductive spinel sintered body is produced. The degree of oxygen deficiency varies depending on the reducing power in the reducing atmosphere, but with the reducing power of the ordinary carbon atmosphere, only oxygen in TiO 2 or Cr 2 O 3 is lost, and oxygen in the spinel. Will not be lost.
[0017]
The temperature at which the sintered body is sintered is preferably 1500 to 1650 ° C. If the temperature is lower than 1500 ° C., densification becomes insufficient, and if it is higher than 1650 ° C., the sintered body may be decomposed. The temperature at which the sintered sintered body is further subjected to heat treatment may be the same as the temperature at which sintering is performed, but in the case of hot isostatic pressure treatment (HIP treatment), 1400 to 1650 ° C. is preferable, and from 1400 ° C. If the pressure is lower or higher than 1650 ° C., the effect of the HIP treatment is small, and if the pressure at that time is lower than 1800 kg / cm 2 , the effect of the HIP treatment is also small.
[0018]
Impurity components such as SiO 2 , CaO, Na 2 O, Fe 2 O 3 and the like contained in the obtained spinel sintered body are preferably 3% by weight or less, and more than 3% by weight, for example, a semiconductor manufacturing apparatus This is not preferable because it causes problems such as insulation failure in the device. In addition, the porosity of the obtained spinel sintered body is preferably 1% or less, and when the porosity exceeds 1%, there are many pores in the sintered body. The corrosion reaction of the halogen-based plasma gas occurs vigorously in the pores, and the surface is significantly corroded, which is not preferable.
[0019]
Next, a dielectric layer is produced by processing the obtained spinel sintered body, and the dielectric layer is adhered to the upper surface of the ceramic substrate on which the electrode is formed, or the obtained dielectric layer is attached to the electrode. A monopolar or bipolar electrostatic chuck is fabricated by bonding to the upper surface or forming an electrode on the lower surface of the dielectric layer. In addition, although the dielectric layer is manufactured by sintering in the above, it may be formed by spraying or sputtering on the surface of a substrate such as ceramics or metal, and reduced in a reducing atmosphere. Good.
[0020]
If the electrostatic chuck is manufactured by the method described above, an electrostatic chuck having a dielectric layer having conductivity and corrosion resistance can be obtained.
[0021]
【Example】
Examples of the present invention will be specifically described below together with comparative examples to describe the present invention in more detail.
[0022]
(Examples 1-7)
(1) Fabrication of electrostatic chuck A 99% pure MgAl 2 O 4 powder and a 99.9% pure MgO powder were prepared so that the ratio of MgO / Al 2 O 3 was as shown in Table 1, and TiO was used. 2 or Cr 2 O 3 powder was added so that the addition ratio was as shown in Table 1, ethanol was added thereto, and the mixture was pulverized for 72 hours by a ball mill.
[0023]
The mixed powder obtained by drying the resultant is subjected to CIP treatment and molded to φ250 × 6 mmt, and the molded body is sintered at a temperature of 1500 to 1650 ° C. in a reducing atmosphere (Examples 1 to 4). And sintered at a temperature of 1500 to 1650 ° C. and further subjected to HIP treatment at a pressure of 1800 kg / cm 2 at a temperature of 1400 to 1650 ° C. in a reducing atmosphere (Examples 5 to 7) to produce a spinel sintered body did. These sintered bodies were processed into φ200 × 2 mmt to produce dielectric layers.
[0024]
An electrode is formed by printing and baking Ag paste on one surface of the obtained dielectric layer, and the other surface is polished so that the surface roughness Ra is 0.34 μm. An electrostatic chuck was prepared by adhering to a dyed (anodized) Al base with an adhesive.
[0025]
(2) Evaluation The bending strength of the obtained spinel sintered body was measured by a three-point bending test method. Further, the electric conductivity of the dielectric layer of the obtained electrostatic chuck was measured by a direct current three-terminal method. Further, the obtained electrostatic chuck is incorporated into a parallel plate electrode type plasma etching apparatus, and a circuit formed on the silicon wafer is destroyed whether or not the silicon wafer is attracted by applying a charge of 1 kV. I investigated whether or not. Furthermore, a plasma gas having a frequency of 2.45 GHz, an output of 800 W, and a volume ratio of CF 4 to O 2 of 4: 1 is etched on the adsorption surface for 40 minutes, and the etching rate of the dielectric layer after the etching is adjusted. Calculation was based on the reduced weight of the dielectric layer. The results are shown in Table 1.
[0026]
(Comparative Examples 1-7)
For comparison, in Comparative Examples 1, 2, 5, and 6, except that the ratio of MgO / Al 2 O 3 in the dielectric layer was out of the range of the present invention, in Comparative Examples 3 and 4, the addition rate of TiO 2 In Comparative Example 7, an electrostatic chuck was prepared and evaluated in the same manner as in Example except that the dielectric layer was alumina. The results are also shown in Table 1.
[0027]
[Table 1]
[0028]
As is apparent from Table 1, all the examples of the electric conductivity of the dielectric layer were within the scope of the present invention. For this reason, all the adsorptivity of the silicon wafer was good. Further, the etching rates for the halogen-based plasma gas are all 5 μm / hr or less, which is much better than the alumina of the comparative example 7, and the addition rate is small even if the addition rate of TiO 2 is large. It was not inferior to. This indicates that the electrostatic chuck according to the present invention can be attracted regardless of the thickness of the dielectric layer, and can be an electrostatic chuck on which a dielectric layer having corrosion resistance is formed.
[0029]
On the other hand, in Comparative Examples 1, 2, 5, and 6, since the ratio of MgO / Al 2 O 3 is outside the range of the present invention, the strength of the dielectric layer was low, and the subsequent evaluation was not performed. In Comparative Example 3, since the addition rate of TiO 2 was too low, the electrical conductivity was low, the silicon wafer could not be adsorbed, and the adsorbability was poor. In Comparative Example 4, since the addition rate of the TiO 2 is too large, although the adsorptive good, circuit electrical conductivity is too high has shorted circuit breakdown gone occur, yet the TiO 2-x Corrosion resistance was also bad because the simple thing remained. In Comparative Example 7, not only the corrosion resistance was poor, but also the adsorbability was poor because the dielectric layer was thick.
[0030]
【The invention's effect】
As described above, the electrostatic chuck according to the present invention can be an electrostatic chuck having a dielectric layer having conductivity and good corrosion resistance.
As a result, the electrostatic chuck can be adsorbed regardless of the thickness of the dielectric layer, and it can be changed to the required electrical conductivity by adjusting the content of TiO 2-x or Cr 2 O 3-x. It can be used as an electrostatic chuck.
Claims (4)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001038132A JP4585129B2 (en) | 2001-02-15 | 2001-02-15 | Electrostatic chuck |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001038132A JP4585129B2 (en) | 2001-02-15 | 2001-02-15 | Electrostatic chuck |
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| Publication Number | Publication Date |
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| JP2002246452A JP2002246452A (en) | 2002-08-30 |
| JP4585129B2 true JP4585129B2 (en) | 2010-11-24 |
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| JP5192221B2 (en) * | 2007-11-30 | 2013-05-08 | 太平洋セメント株式会社 | Ceramic sintered body and electrostatic chuck using the same |
| JP5188898B2 (en) * | 2008-07-11 | 2013-04-24 | 太平洋セメント株式会社 | Ceramic sprayed coating and corrosion resistant member using the same |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2501504B2 (en) * | 1990-12-28 | 1996-05-29 | 日本碍子株式会社 | Electrostatic chuck |
| DE19515490A1 (en) * | 1995-04-27 | 1996-10-31 | Abb Patent Gmbh | Ceramic material and process for its manufacture |
| JP3559426B2 (en) * | 1997-05-30 | 2004-09-02 | 京セラ株式会社 | Corrosion resistant materials |
| JP3527839B2 (en) * | 1998-01-28 | 2004-05-17 | 京セラ株式会社 | Components for semiconductor device manufacturing equipment |
| JP3369505B2 (en) * | 1999-04-13 | 2003-01-20 | 太平洋セメント株式会社 | Electrostatic chuck |
| JP4368021B2 (en) * | 2000-01-18 | 2009-11-18 | 太平洋セメント株式会社 | Corrosion resistant ceramic material |
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