WO2010068635A2 - Filled polymer composition for etch chamber component - Google Patents
Filled polymer composition for etch chamber component Download PDFInfo
- Publication number
- WO2010068635A2 WO2010068635A2 PCT/US2009/067218 US2009067218W WO2010068635A2 WO 2010068635 A2 WO2010068635 A2 WO 2010068635A2 US 2009067218 W US2009067218 W US 2009067218W WO 2010068635 A2 WO2010068635 A2 WO 2010068635A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- composition
- particle filler
- plasma
- polymer composition
- group
- 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.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/08—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/02—Non-macromolecular additives
- C09J11/04—Non-macromolecular additives inorganic
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
- Y10T428/2852—Adhesive compositions
- Y10T428/2857—Adhesive compositions including metal or compound thereof or natural rubber
Definitions
- Embodiments of the present invention relate to the field of filled polymer materials. More particularly, embodiments of the present invention related to a filled polymer composition for use in etch chamber components.
- Polymer materials used in etch chamber components are exposed to plasmas within the etch chamber during both substrate etching and chamber cleaning processes. For example, plasma etch residues and byproducts formed on chamber components can pose a chronic problem, and therefore the etch chamber is periodically cleaned to prevent process drift and particle generation. As a result, the polymer materials can themselves become a source of particle adders and also must be periodically replaced because they are eroded by the various etching and cleaning plasmas.
- Embodiments of the present invention disclose a filled polymer composition including a particle filler dispersed in a polymer matrix.
- the particle filler can be Nb 2 O 5 , YF 3 , AlN, Al, SiC, Si 3 N 4 , rare earth oxides, and combinations thereof.
- the filled polymer composition can be utilized in any chamber or service environment exposed to various plasmas to prolong the service life, to improve the application temperature, to advance process uniformity, to decrease the amount of formed particles, and to decrease metal contamination.
- the filled polymer composition is utilized as a bonding adhesive for an electrostatic chuck, bonding adhesive for a shower head, bonding adhesive for a liner, a sealing material, an O-ring, or a plastic component.
- FIG. IA and FIG. IB are isometric view illustrations of an etch chamber.
- FIG. 1C includes an overhead view illustration and close-up isometric view illustration of a showerhead backside and O-ring.
- FIG. ID is an overhead view illustration of an electrostatic chuck backside.
- FIG. 2A - FIG. 2B are illustrations of the surface morphology of the erosion surface of an adhesive exposed to a CH 4 /CHF 3 plasma for 5 RF hours.
- FIG. 3A - FIG. 3B are illustrations of the surface morphology of the erosion surface of an adhesive exposed to a HBr/Cl 2 /CF 4 / ⁇ 2 plasma for 6.5 RF hours.
- FIG. 4A - FIG. 4B are illustrations of the surface morphology of the erosion surface of an adhesive exposed to a SiCl 4 plasma for 12 RF hours.
- Embodiments of the present invention disclose a filled polymer composition and applications of the filled polymer composition in plasma chamber components.
- Various embodiments described herein are described with reference to figures. In the following description, numerous specific details are set forth, such as specific configurations, compositions, and processes, etc., in order to provide a thorough understanding of the present invention. However, certain embodiments may be practiced without one or more of these specific details, or in combination with other known methods and configurations. In other instances, well-known processes and manufacturing techniques have not been described in particular detail in order to not unnecessarily obscure the present invention.
- Embodiments of the invention disclose a filled polymer composition including a particle filler dispersed in a polymer matrix.
- the particle filler has an average particle size of 10 nm - 10 ⁇ m, and can be a rare earth oxide, Nb 2 O 5 , YF 3 , AlN, SiC, Si 3 N 4 , and combinations thereof.
- the particle filler can be a metal such as Al powder of the same average particle size.
- the particle filler is tightly combined with the polymer matrix to provide a composition with improved properties including excellent plasma resistance, material structure stability (low outgassing), high temperature application, improved thermal properties (thermal conductivity and thermal expansion), advanced mechanical properties (elongation, elastic modulus, lap share, tensile strength) and much reduced particle generation potential.
- the filled polymer composition can be utilized in any chamber or service environment exposed to various plasmas to prolong the service life, to improve the application temperature, to advance process uniformity, to decrease the amount of formed particles, and to decrease metal contamination.
- the filled polymer composition is utilized as a bonding adhesive for electrostatic chuck, a bonding adhesive for shower head, a bonding adhesive for liner, a sealing material, an O-ring, or a plastic component.
- the term "rare earth oxide” means an oxide of the rare earth elements in the Periodic Table of Elements called the Lanthanide Series that runs from atomic number 57 to 71, and additionally elements yttrium #39 and scandium #21 because they share similar properties to the elements of the Lanthanide Series.
- the particle filler can be a rare earth oxide such as, but not limited to, Y 2 O 3 , Sc 2 O 3 , Er 2 O 3 , Nd 2 O 3 , Sm 2 O 3 and Yb 2 O 3 .
- the polymer matrix can be a variety of materials.
- the polymer matrix may be fluorinated carbon based, polyimide based, ether ketone based, and silicon based including partially and fully fluorinated silicon.
- the polymer matrix is a perfluoroelastomer, thermosetting silicone, a thermoplastic acrylic, or poly(etheretherketone) (PEEK).
- FIG. IA and FIG. IB are illustrations of an etch chamber in accordance with an embodiment of the invention.
- the chamber illustrated in FIG. IA may be a CENTURA ENABLER ETCH.TM. chamber available from Applied Materials, Inc. of Santa Clara, Calif.
- the chamber illustrated in FIG. IB may be a PRODUCER ETCH.TM. chamber available from Applied Materials, Inc. of Santa Clara, Calif.
- the etch chamber 100 can include a chamber lid configured to provide plasma or energy from a plasma generator (not shown) and gas from the process gas source a gas conduit (not shown).
- a gas shower head 102 may be bonded to the chamber lid utilizing an adhesive comprising a filled polymer composition in accordance with embodiments of the invention.
- the base of the chamber contains an electrostatic chuck 104 which is attached to a power source (not shown).
- the electrostatic chuck 104 can be bonded to a support utilizing an adhesive comprising a filled polymer composition.
- a chamber liner 106 can be bonded to the chamber utilizing an adhesive comprising a filled polymer composition in accordance with embodiments of the invention.
- the filled polymer composition is employed as a bonding adhesive, for example, for an electrostatic chuck, shower head, and/or liner, it may be preferable to adjust the materials properties of the filled polymer composition to minimize the coefficient of thermal expansion (CTE) mismatch between a metal and a ceramic.
- CTE coefficient of thermal expansion
- a higher tensile elongation %, higher tensile strength, and lower Young's Modulus are desirable for electrostatic chuck bonding application.
- the filled polymer composition may exhibit a tensile elongation % above 190 %, a tensile strength above 2.2 MPa, and Young's Modulus below 2.0 MPa.
- the filled polymer composition may exhibit a tensile elongation % above 105 %, and Young's Modulus below 3.8 MPa.
- the filled polymer composition is not limited to adhesive applications.
- the filled polymer composition can be a seal such as an O-ring.
- FIG. 1C includes an overhead view illustration and close-up isometric view illustration of a showerhead backside and O-ring.
- the filled polymer composition is an O-ring 108 located on a showerhead 102.
- the filled polymer composition can be an insert plastic part such as a cathode insulator.
- FIG. ID is an overhead view illustration of an electrostatic chuck backside.
- the filled polymer composition is a cathode insulator 110 located on an electrostatic chuck 104.
- tensile elongation % may not be a necessary property, and instead tensile strength is more important for a cathode insulator or similar high performance plastic application.
- the filled polymer composition can be implemented into a variety of critical etch chamber components to prolong the service life, to improve the application temperature, to advance process uniformity, to decrease the amount of formed particles, and to reduce metal contamination.
- the filled polymer composition can be applied to other service environments, not limited to plasma chambers, where the excellent plasma resistance performance and adjustable materials properties are required.
- the filled polymer composition can be prepared utilizing a number of known techniques depending upon application.
- the filled polymer composition can be prepared by adding a particle filler to a solution including a dissolved polymer composition.
- the particle filler can be uniformly dispersed in the solution utilizing a dispersing agent, cast, cured, and post-cure baked as is known in the art.
- particulate polymer and particle filler can be physically mixed together by stirring or ball milling as is known in the art.
- embodiments of the invention disclose a filled polymer composition in which the particle size of the particle filler can be varied to obtain the required materials properties.
- the particle filler has an average particle size of 10 nm - 10 ⁇ m.
- the particle filler has a particle size small enough that the particle itself does not become a contaminant.
- the particle filler may have a particles size of less than 1 ⁇ m. It has been found that below approximately 10 nm particles can be difficult to evenly disperse. Larger particles are beneficial when matching of thermal conductivity of the filled polymer composition to another material is desired.
- embodiments of the invention disclose a filled polymer composition in which the volume % of the particle filler can be varied to obtain the required materials properties.
- the filled polymer composition includes 50% - 75% particle filler by volume.
- Maintaining the volume density of the particle filler is particularly beneficial for applications where the filled polymer composition is exposed to significant plasma etching, such as, but not limited to, a bonding adhesive for a shower head, electrostatic chuck and/or liner.
- the specific volume composition obtains the synergetic effect of changing the characteristic etch rate of the entire filled polymer composition. While individually, the polymer matrix and particle filler possess different characteristic etch rates to specific plasma chemistries, when the filled polymer composition includes 50% - 75% particle filler by volume the etch rate of the entire filled polymer composition is improved. This is accomplished by controlling the volume density of particles such that the particles touch one another, and can further bond or coalesce when exposed to a plasma process such as a plasma etching or cleaning process.
- Plasma chamber components comprising a filled polymer composition in accordance with embodiments of the invention may demonstrate increased plasma resistance which can be measured by surface erosion and surface morphology.
- Table I includes normalized surface erosion data of filled polymer compositions for adhesive applications in accordance with the present invention, compared to the base polymer composition of thermosetting silicone and a thermoplastic acrylic polymer filled with Al mesh and TiB 2 filler. Table I. Normalized Surface Erosion
- an embodiment in which an adhesive comprises a filled polymer composition containing 50% - 75% by volume Y 2 O 3 filler particles with an average particle size of 380 nm embedded in a thermosetting silicone matrix exhibits the lowest normalized surface erosion for the three plasma conditions.
- thermosetting silicone experiences 2 times
- Fluorine chemistries such as CF 4 /CHF 3 are etch chemistries often utilized in dielectric substrate etching.
- HBr/Cl 2 /CF 4 /O 2 chemistries are etch chemistries often utilized in conductive substrate etching.
- O 2 and SiCl 4 chemistries are etch chamber clean chemistries.
- SiCl 4 in particular is utilized as an etch chamber clean chemistry to remove AlF contamination from chamber components which forms during dielectric and conductive surface etching.
- FIG. 2A - FIG. 2B are illustrations of the surface morphology of the erosion surface of an adhesive exposed to a CH 4 /CHF 3 plasma for 5 RF hours.
- a thermosetting silicone polymer matrix results in an erosion surface with a course surface morphology.
- FIG. 2B is a filled polymer composition in accordance with embodiments of the present invention including a thermosetting silicone polymer matrix and a Y 2 O 3 particle filler.
- the surface morphology is largely improved after fluorine plasma etch, which reduces metal contamination and particle counts.
- FIG. 3A - FIG. 3B are illustrations of the surface morphology of the erosion surface of an adhesive exposed to a HBr/Cl 2 /CF 4 /O 2 plasma for 6.5 RF hours.
- a thermosetting silicone polymer matrix results in an erosion surface with a course surface morphology.
- FIG. 3B is a filled polymer composition in accordance with embodiments of the present invention including a thermosetting silicone polymer matrix and a Y 2 O 3 particle filler.
- FIG. 3B only the Y 2 O 3 particle filler was left on the surface and the thermosetting silicone polymer matrix was etched, meaning that the Y 2 O 3 particle filler played a major role in improving the plasma resistance.
- FIG. 4A - FIG. 4B are illustrations of the surface morphology of the erosion surface of an adhesive exposed to a SiCl 4 plasma for 12 RF hours.
- a thermosetting silicone polymer matrix is shown in FIG. 4A.
- FIG. 4B is a filled polymer composition in accordance with embodiments of the present invention including a thermosetting silicone polymer matrix and a Y 2 O 3 particle filler. As shown in FIG. 4B, the Y 2 O 3 particle filler was exposed and most of the surface thermosetting silicone polymer matrix was etched, meaning that the Y 2 O 3 particle filler played a major role in improving the plasma resistance.
- the filled polymer composition of the present invention is implemented in a plasma chamber as an O-ring.
- the filled polymer composition can contain approximately 15% by volume Y 2 O 3 particle filler in a perfluoroelastomer polymer matrix, which exhibits approximately 4 times less erosion than an unfilled perfluoroelastomer polymer matrix when exposed to a CF 4 plasma, approximately 7 times less erosion when exposed to an O 2 plasma, and approximately 5 times less erosion when exposed to a CF 4 /O 2 plasma.
- the improved plasma resistance improves the lifetime, reduces contamination, and particle generation.
- the filled polymer composition of the present invention is implemented in a plasma chamber as a high performance plastic, such as a cathode insulator.
- the filled polymer composition includes Y 2 O 3 particle filler in a PEEK polymer matrix.
- the particle filler improves the tensile strength, tensile modulus, flexural modulus, and surface resistivity compared to an unfilled PEEK cathode insulator.
- surface erosion is improved over 100 times compared to an unfilled PEEK composition when exposed to an O 2 plasma for 14 RF hours.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Toxicology (AREA)
- General Health & Medical Sciences (AREA)
- Inorganic Chemistry (AREA)
- Drying Of Semiconductors (AREA)
- Container, Conveyance, Adherence, Positioning, Of Wafer (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Sealing Material Composition (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
Claims
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN200980149880.6A CN102245689B (en) | 2008-12-10 | 2009-12-08 | Filling polymer compositions for etching chamber components |
| JP2011540842A JP2012511834A (en) | 2008-12-10 | 2009-12-08 | Filling polymer composition for etching chamber parts |
| KR1020157010999A KR101739926B1 (en) | 2008-12-10 | 2009-12-08 | Filled polymer composition for etch chamber component |
| SG2011042140A SG172056A1 (en) | 2008-12-10 | 2009-12-08 | Filled polymer composition for etch chamber component |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12149008P | 2008-12-10 | 2008-12-10 | |
| US61/121,490 | 2008-12-10 | ||
| US12/632,712 | 2009-12-07 | ||
| US12/632,712 US20100140222A1 (en) | 2008-12-10 | 2009-12-07 | Filled polymer composition for etch chamber component |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2010068635A2 true WO2010068635A2 (en) | 2010-06-17 |
| WO2010068635A3 WO2010068635A3 (en) | 2010-08-19 |
Family
ID=42229913
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2009/067218 Ceased WO2010068635A2 (en) | 2008-12-10 | 2009-12-08 | Filled polymer composition for etch chamber component |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US20100140222A1 (en) |
| JP (1) | JP2012511834A (en) |
| KR (2) | KR20110100646A (en) |
| CN (2) | CN103497457A (en) |
| SG (1) | SG172056A1 (en) |
| TW (2) | TW201514223A (en) |
| WO (1) | WO2010068635A2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102190984A (en) * | 2011-04-08 | 2011-09-21 | 河北金天塑胶新材料有限公司 | Hot-melt adhesive for steel-plastic composite pipe |
| JP2014503611A (en) * | 2010-11-15 | 2014-02-13 | アプライド マテリアルズ インコーポレイテッド | Adhesive material used to join chamber components |
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| CN102408663B (en) * | 2011-08-25 | 2015-03-25 | 上海亚明灯泡厂有限公司 | Insulating heat-conducting ABS composite material doped with aluminum nitride and preparation thereof |
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| US10570257B2 (en) | 2015-11-16 | 2020-02-25 | Applied Materials, Inc. | Copolymerized high temperature bonding component |
| US11572617B2 (en) | 2016-05-03 | 2023-02-07 | Applied Materials, Inc. | Protective metal oxy-fluoride coatings |
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| US20230197417A1 (en) * | 2021-12-17 | 2023-06-22 | Applied Materials, Inc. | Corrosion resistant polymer coatings for manufacturing equipment components |
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-
2009
- 2009-12-07 US US12/632,712 patent/US20100140222A1/en not_active Abandoned
- 2009-12-08 WO PCT/US2009/067218 patent/WO2010068635A2/en not_active Ceased
- 2009-12-08 KR KR1020117016068A patent/KR20110100646A/en not_active Ceased
- 2009-12-08 SG SG2011042140A patent/SG172056A1/en unknown
- 2009-12-08 CN CN201310432769.6A patent/CN103497457A/en active Pending
- 2009-12-08 CN CN200980149880.6A patent/CN102245689B/en active Active
- 2009-12-08 JP JP2011540842A patent/JP2012511834A/en active Pending
- 2009-12-08 KR KR1020157010999A patent/KR101739926B1/en active Active
- 2009-12-09 TW TW103145777A patent/TW201514223A/en unknown
- 2009-12-09 TW TW098142126A patent/TW201033262A/en unknown
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014503611A (en) * | 2010-11-15 | 2014-02-13 | アプライド マテリアルズ インコーポレイテッド | Adhesive material used to join chamber components |
| CN107611065A (en) * | 2010-11-15 | 2018-01-19 | 应用材料公司 | It is suitable for connecting the attachment material and semiconductor chamber component of multiple semiconductor chamber components |
| KR101861600B1 (en) * | 2010-11-15 | 2018-05-28 | 어플라이드 머티어리얼스, 인코포레이티드 | An adhesive material used for joining chamber components |
| CN107611065B (en) * | 2010-11-15 | 2021-02-26 | 应用材料公司 | Adhesion material and semiconductor chamber component |
| CN102190984A (en) * | 2011-04-08 | 2011-09-21 | 河北金天塑胶新材料有限公司 | Hot-melt adhesive for steel-plastic composite pipe |
| CN102190984B (en) * | 2011-04-08 | 2012-11-14 | 河北金天塑胶新材料有限公司 | Hot-melt adhesive for steel-plastic composite pipe |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2012511834A (en) | 2012-05-24 |
| KR20110100646A (en) | 2011-09-14 |
| US20100140222A1 (en) | 2010-06-10 |
| CN102245689B (en) | 2014-04-02 |
| CN103497457A (en) | 2014-01-08 |
| TW201514223A (en) | 2015-04-16 |
| KR20150054008A (en) | 2015-05-19 |
| SG172056A1 (en) | 2011-07-28 |
| TW201033262A (en) | 2010-09-16 |
| CN102245689A (en) | 2011-11-16 |
| WO2010068635A3 (en) | 2010-08-19 |
| KR101739926B1 (en) | 2017-05-25 |
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