US20070111642A1 - Apparatus and methods for slurry cleaning of etch chambers - Google Patents
Apparatus and methods for slurry cleaning of etch chambers Download PDFInfo
- Publication number
- US20070111642A1 US20070111642A1 US11/272,844 US27284405A US2007111642A1 US 20070111642 A1 US20070111642 A1 US 20070111642A1 US 27284405 A US27284405 A US 27284405A US 2007111642 A1 US2007111642 A1 US 2007111642A1
- Authority
- US
- United States
- Prior art keywords
- abrasive slurry
- atomized
- abrasive
- inlet
- slurry
- 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.)
- Abandoned
Links
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- 238000000034 method Methods 0.000 title claims abstract description 41
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- 239000011261 inert gas Substances 0.000 claims description 6
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 238000005530 etching Methods 0.000 claims description 5
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- 238000002156 mixing Methods 0.000 claims description 2
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims description 2
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- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 239000000919 ceramic Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
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- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
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- 238000013461 design Methods 0.000 description 2
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- 238000010008 shearing Methods 0.000 description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 2
- 229910010271 silicon carbide Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- JRZKNHITLINYHV-UHFFFAOYSA-N 1,2,3,4,5-pentachloronaphthalene Chemical compound ClC1=CC=CC2=C(Cl)C(Cl)=C(Cl)C(Cl)=C21 JRZKNHITLINYHV-UHFFFAOYSA-N 0.000 description 1
- NAQWICRLNQSPPW-UHFFFAOYSA-N 1,2,3,4-tetrachloronaphthalene Chemical compound C1=CC=CC2=C(Cl)C(Cl)=C(Cl)C(Cl)=C21 NAQWICRLNQSPPW-UHFFFAOYSA-N 0.000 description 1
- 239000010963 304 stainless steel Substances 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 229910052580 B4C Inorganic materials 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229910000589 SAE 304 stainless steel Inorganic materials 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 238000005270 abrasive blasting Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
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- 229910052787 antimony Inorganic materials 0.000 description 1
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- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910000420 cerium oxide Inorganic materials 0.000 description 1
- 239000011045 chalcedony Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 125000003636 chemical group Chemical group 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
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- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
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- 150000007522 mineralic acids Chemical class 0.000 description 1
- 150000002898 organic sulfur compounds Chemical class 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 239000013618 particulate matter Substances 0.000 description 1
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- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- ABTOQLMXBSRXSM-UHFFFAOYSA-N silicon tetrafluoride Chemical class F[Si](F)(F)F ABTOQLMXBSRXSM-UHFFFAOYSA-N 0.000 description 1
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- MTPVUVINMAGMJL-UHFFFAOYSA-N trimethyl(1,1,2,2,2-pentafluoroethyl)silane Chemical compound C[Si](C)(C)C(F)(F)C(F)(F)F MTPVUVINMAGMJL-UHFFFAOYSA-N 0.000 description 1
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Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24C—ABRASIVE OR RELATED BLASTING WITH PARTICULATE MATERIAL
- B24C5/00—Devices or accessories for generating abrasive blasts
- B24C5/02—Blast guns, e.g. for generating high velocity abrasive fluid jets for cutting materials
- B24C5/04—Nozzles therefor
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24C—ABRASIVE OR RELATED BLASTING WITH PARTICULATE MATERIAL
- B24C11/00—Selection of abrasive materials or additives for abrasive blasts
- B24C11/005—Selection of abrasive materials or additives for abrasive blasts of additives, e.g. anti-corrosive or disinfecting agents in solid, liquid or gaseous form
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24C—ABRASIVE OR RELATED BLASTING WITH PARTICULATE MATERIAL
- B24C3/00—Abrasive blasting machines or devices; Plants
- B24C3/32—Abrasive blasting machines or devices; Plants designed for abrasive blasting of particular work, e.g. the internal surfaces of cylinder blocks
- B24C3/325—Abrasive blasting machines or devices; Plants designed for abrasive blasting of particular work, e.g. the internal surfaces of cylinder blocks for internal surfaces, e.g. of tubes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24C—ABRASIVE OR RELATED BLASTING WITH PARTICULATE MATERIAL
- B24C7/00—Equipment for feeding abrasive material; Controlling the flowability, constitution, or other physical characteristics of abrasive blasts
- B24C7/0007—Equipment for feeding abrasive material; Controlling the flowability, constitution, or other physical characteristics of abrasive blasts the abrasive material being fed in a liquid carrier
- B24C7/0038—Equipment for feeding abrasive material; Controlling the flowability, constitution, or other physical characteristics of abrasive blasts the abrasive material being fed in a liquid carrier the blasting medium being a gaseous stream
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/67—Apparatus specially adapted for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus specially adapted for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components ; Apparatus not specifically provided for elsewhere
- H01L21/67005—Apparatus not specifically provided for elsewhere
- H01L21/67011—Apparatus for manufacture or treatment
- H01L21/67017—Apparatus for fluid treatment
- H01L21/67028—Apparatus for fluid treatment for cleaning followed by drying, rinsing, stripping, blasting or the like
- H01L21/6704—Apparatus for fluid treatment for cleaning followed by drying, rinsing, stripping, blasting or the like for wet cleaning or washing
- H01L21/67051—Apparatus for fluid treatment for cleaning followed by drying, rinsing, stripping, blasting or the like for wet cleaning or washing using mainly spraying means, e.g. nozzles
Definitions
- the invention is directed to cleaning apparatus and methods, particularly, but not limited to, apparatus and methods for cleaning products and chambers made during semiconductor manufacturing.
- Removal of contaminants from etch chamber components traditionally uses carbon dioxide pellet blasting, abrasive bead blasting, solvents, strong oxidizers, inorganic acids/bases or high temperature thermal decomposition. Depending on the contaminant/substrate combination, these produce marginal results in contaminant removal and providing high cleanliness surfaces for chamber reuse. These methods may also damage the substrate during the cleaning process particularly when using conventional mechanical cleaning methods for anodized and coated aluminum substrates. More recent designs of chamber components make use of plasma sprayed dielectric coatings such as Al 2 O 3 , ZrO 2 , and Y 2 O 3 . These coatings are applied to ceramic and anodized aluminum substrates where coating adhesion is marginal at best and are easily damaged during cleaning due to the aggressive nature of conventional abrasive blasting techniques.
- apparatus and methods are presented which overcome or reduce deficiencies associated with previous apparatus and methods in cleaning semiconductor etching chambers and components.
- a first aspect of the invention is an apparatus, one apparatus comprising:
- Apparatus within the invention include those wherein the container may have an agitator adapted to maintain the abrasive particles well dispersed.
- “Well dispersed”, as used herein, means that the abrasive slurry may be a homogenous mixture of all ingredients.
- the source of atomizing fluid may be selected from a membrane unit, an absorption unit, a cryogenic unit, a container of fluid, a compressor, a pipeline, a gas cabinet, and combinations thereof.
- the source of atomizing fluid may comprise a source of one or more inert gases and combinations thereof.
- the inert gas may be selected from any gas that would be considered inert for the cleaning process, including, but not limited to, nitrogen, argon, air, nitrogen enriched air, noble gases other than argon, and combinations thereof.
- the atomizing head may comprise a venturi.
- Apparatus may comprise a pressure regulator adapted to adjust pressure of the atomizing fluid entering the atomizing head.
- the pressure regulator may be adapted to adjust pressure of the atomized abrasive slurry exiting the atomizing head.
- Another aspect of the invention is a method of cleaning, one method comprising directing an atomized abrasive slurry onto at least some internal surfaces of a semiconductor etching chamber or chamber components.
- Methods of the invention include those wherein the directing comprises controlling pressure of the atomized abrasive slurry.
- the pressure may generally be controlled within a pressure ranging from about 25 to about 150 psig. Pressures higher than 150 psig may be used if necessary to remove debris and the underlying substrate is not damaged.
- the density of the atomized abrasive slurry may need to be reduced; pressures lower than 25 psig may not be able to provide the desired cleaning efficiency, but may be used if the density of the atomized abrasive slurry is increased.
- Methods of the invention include those methods wherein the directing step comprises controlling density of the atomized abrasive slurry.
- the directing step comprises controlling density of the atomized abrasive slurry.
- ways are available for controlling density of the atomized slurry, including adding more liquid to the abrasive slurry, reducing the amount and/or density of the abrasive particles in the abrasive slurry, reducing the density of the atomizing fluid and/or increasing its flow rate, and combinations of these.
- the density of the atomized abrasive slurry may be controlled within a density ranging from about 0.01 gm/cc to about 0.2 gm/cc.
- Other methods of the invention include controlling momentum of the atomized abrasive slurry exiting the atomizing head.
- Methods of the invention include controlling momentum of the atomized abrasive slurry at momentum ranging from about 100,000 gm-cm/sec to about 300,000 gm-cm/sec.
- Other methods may include maintaining the abrasive slurry in the abrasive slurry container in well dispersed state, and methods wherein the composition of the abrasive slurry in the container is controlled.
- FIGS. 1 and 2 are schematic side elevation views of first and second apparatus embodiments according to the present invention.
- Apparatus of the invention comprise an atomizing head functioning to produce an atomized abrasive slurry.
- the head comprises an abrasive slurry inlet, an atomizing fluid inlet, and an atomized abrasive slurry outlet.
- the atomizing head may include any internal volume capable of producing an atomized abrasive slurry, including a venturi, a converging-diverging nozzle, a converging nozzle, and other nozzle configurations.
- Apparatus of the present invention are concerned with the third category of atomization.
- Internal atomization is characterized by confinement of the liquid and atomizing fluid in a contacting chamber.
- the mode of introduction of the two fluids into this chamber can vary considerably and has a direct influence on the characteristics of the atomized slurry that exits from the chamber.
- the internal geometry of this chamber also affects the specific characteristics of the liquid/atomizing fluid mixture.
- This mode of atomization generally affords an excellent quality of atomization, that is, an atomized slurry composed of very small slurry droplets with a very narrow droplet size distribution about these small diameters.
- this atomization quality is naturally a function of the atomizing fluid delivery rate employed and the pressure level prevailing in the interior of the atomizing chamber.
- the atomized slurry is created mainly by shearing of the jet of liquid slurry by the atomizing fluid.
- the geometry of the outlets for the two fluids completely determines the quality of the atomization, and droplet size analysis of the drops resulting from the contact may show a relatively wide diameter distribution (simultaneous-presence of small and large droplets).
- FIG. 1 is a schematic side elevation view of one apparatus embodiment 100 according to the present invention, comprising an atomizing head 2 having an atomizing fluid inlet 4 , an abrasive slurry inlet 6 , and an atomized abrasive slurry outlet 8 .
- Atomizing head 2 may be made from any suitable material or combination of materials, such as metal, plastic, and combinations thereof. Suitable metals include aluminum, stainless steels, such as 304 stainless steel. The stainless steel may be electropolished, but this is not a requirement of the invention.
- the internal flow channels include a converging nozzle 10 , a parallel throat section 12 , and a diverging nozzle 14 .
- Throat 12 includes in this embodiment an inlet port or orifice 16 for abrasive slurry, which is drawn into throat 12 by negative pressure caused by flowing fluidizing fluid.
- Abrasive slurry may be drawn up from one or more abrasive slurry containers 20 , and head 2 may have one or more fluid connections to one or more sources of fluidizing fluid 18 .
- this particular flow configuration represents a venturi, the invention is not so limited.
- atomizing fluid inlet may be comprised of one, two, or more than two inlet orifices, as may abrasive inlet orifice 16 .
- atomizing fluid inlet may be comprised of one, two, or more than two inlet orifices, as may abrasive inlet orifice 16 .
- FIG. 2 is a schematic side elevation view of another apparatus embodiment 200 according to the present invention, similar to embodiment 100 illustrated in FIG. 1 , comprising an atomizing head 22 having an atomizing fluid inlet 4 , an abrasive slurry inlet 6 , and an atomized abrasive slurry outlet 8 .
- the internal flow channels include a more streamlined converging-diverging nozzle 24 , 28 , and a throat 26 .
- Throat 26 also includes in this embodiment an inlet port or orifice 16 for abrasive slurry, which is drawn into throat 26 by negative pressure caused by flowing fluidizing fluid.
- Abrasive slurry may be drawn up from one or more abrasive slurry containers 20 , and head 2 may have one or more fluid connections to one or more sources of fluidizing fluid 18 .
- abrasive slurry container fluidly connected to the abrasive slurry inlet of the atomizing head.
- the container functions to define a space for a slurry comprising water, abrasive particles, and other optional ingredients, depending on the particular cleaning task, for example the type and quantity of debris or deposits to be removed, the underlying substrate composition and hardness, and the properties of any substrate coating, such as a refractory or dielectric coating.
- the abrasive slurry container may be under atmospheric pressure, at a slight vacuum, or at a pressure above atmospheric, although the pressure in the container is not critical.
- the container may be closed or open to the atmosphere. If the container is at a pressure less than or greater than atmospheric the container will necessarily be manufactured to withstand these conditions.
- the container may comprise an outer shell with a bladder arrangement, where abrasive slurry is held inside the bladder. Air or other fluid may be used to force slurry out of the bladder, and a vacuum may assist loading the bladder with the abrasive slurry.
- the configuration of the abrasive slurry container is not critical, as long the abrasive particles are able to be kept suspended, or reasonably so, in the container. There may be occasions when there are more abrasive particles than required for a particular task, in which case not all abrasives particles will need to be suspended. Some may be allowed to settle out to the bottom of the container until needed.
- the materials of construction of the slurry container are not critical.
- the container may be metal, plastic, or some combination thereof.
- a refractory or ceramic container may even be used, and a liner may be used.
- the liner may be a ceramic or plastic material.
- Suspension aids may be used. These may be chemical, mechanical or combination thereof.
- a mechanical suspension aide may comprise one or more stirring or agitating device.
- a chemical suspension aide may comprise one or more suspension aide chemicals. Examples of these latter are discussed further herein.
- Apparatus of the invention may comprise a source of atomizing fluid fluidly connected to the atomizing fluid inlet.
- the source of atomizing fluid is selected from a membrane unit, an absorption unit, a cryogenic unit, a container of fluid, a compressor, a pipeline, a gas cabinet, and combinations thereof.
- the source of atomizing fluid may comprise a source of one or more inert gases and combinations thereof. If used, the inert gas may be selected from sources of nitrogen, argon, air, nitrogen enriched air, noble gases other than argon, and combinations and mixtures thereof.
- the atomizing fluid need not be a pure gas.
- the atomizing fluid may be air, or nitrogen generated by a membrane separation unit producing nitrogen enriched air.
- the source of atomizing fluid is fluidly connected to the atomizing head by one or more conduits, which may include one or more pressure regulators adapted to adjust pressure of the atomizing fluid as it enters the atomizing head.
- the pressure regulator may be adapted to adjust pressure of the atomized abrasive slurry as well.
- the pressure of the source of atomizing fluid may be any pressure required to atomize a particular slurry and perform the cleaning function.
- the pressure of the source of atomizing fluid may be controlled, such as by use of a gas cabinet, or it may be taken from a pipeline where there is little control over the pressure of the atomizing fluid in the pipeline.
- methods of the invention include directing an atomized abrasive slurry onto at least some internal surfaces of a semiconductor etching chamber.
- the methods include generating the atomized abrasive slurry by flowing an atomizing fluid through an atomizing head, as described.
- Generating the atomized abrasive slurry may comprise controlling pressure of the atomized abrasive slurry exiting the atomizing head at a pressure ranging from about 25 to about 150 psig.
- the generating may comprise controlling density of the atomized abrasive slurry to a density ranging from about 0.01 gm/cc to about 0.2 gm/cc.
- the momentum of the atomized abrasive slurry at the workpiece may be controlled by controlling the momentum of the atomized abrasive slurry as it exits the atomizing head.
- the momentum of the atomized abrasive slurry exiting the atomizing head may be controlled with in a range of from about 100,000 gm-cm/sec to about 300,000 gm-cm/sec.
- the momentum of the atomized abrasive slurry as it exits the atomizing head may be controlled by adjusting the pressure of the atomizing fluid as it enters the atomizing head, the amount of slurry entering the atomizing head, the density of the abrasive slurry, or any combination of these.
- the abrasive slurry may be maintained in a well-dispersed state in the abrasive slurry container.
- this means the abrasive slurry may be a homogenous mixture of all ingredients.
- Abrasive particles useful in the invention may be selected from those commonly used in the abrasive art, however, the abrasive particles (size and composition) will be chosen with the degree of surface roughness, coating thickness change, and adhesion properties in mind. In choosing an appropriate abrasive particle, characteristics such as hardness, compatibility with the intended workpiece, particle size, reactivity with the workpiece, as well as heat conductivity may be considered.
- composition of abrasive particles useful in the invention can be divided into two classes: natural abrasives and manufactured abrasives.
- natural abrasives include: diamond, corundum, emery, garnet, buhrstone, chert, quartz, sandstone, chalcedony, flint, quartzite, silica, feldspar, pumice and talc.
- Examples of manufactured abrasives include: boron carbide, cubic boron nitride, fused alumina, ceramic aluminum oxide, heat treated aluminum oxide, alumina zirconia, glass, silicon carbide, iron oxides, tantalum carbide, cerium oxide, tin oxide, titanium carbide, synthetic diamond, manganese dioxide, zirconium oxide, and silicon nitride.
- Abrasive particles useful in the invention typically and preferably have a particle size ranging from about 0.1 micrometer to about 1500 micrometers, more preferably ranging from about 0.1 micrometer to about 1300 micrometers.
- the abrasive particles preferably have an average particle size ranging from about 0.1 micrometer to about 700 micrometers, more preferably ranging from about 1 to about 150 micrometers, particularly preferably from about 1 to about 80 micrometers. It is preferred that abrasive particles used in the invention have a Moh's hardness of at least 8, more preferably above 9; however, for specific applications, softer particles may be used.
- abrasive particle includes agglomerates of individual abrasive particles.
- An abrasive agglomerate is formed when a plurality of abrasive particles are bonded together with a binder to form a larger abrasive particle which may have a specific particulate structure.
- the plurality of particles which form the abrasive agglomerate may comprise more than one type of abrasive particle and a binder.
- fillers are inorganic particulate matter which comprise apparatus which are substantially inert or non-reactive with respect to the surface acted upon by the abrasive.
- active (i.e. reactive) fillers are used, sometimes referred to in the abrasives art as grinding aids.
- These fillers interact beneficially with the workpiece during use.
- the grinding aid may either 1) decrease the friction between the abrasive particles and the workpiece being abraded, 2) prevent the abrasive particle from “capping”, i.e. prevent metal particles from becoming welded to the tops of the abrasive particles, 3) decrease the interface temperature between the abrasive particles and the workpiece or 4) decrease the required grinding force.
- Grinding aids encompass a wide variety of different materials and can be inorganic or organic based.
- Examples of chemical groups of grinding aids useful in this invention include waxes, organic halide compounds, halide salts and metals and their alloys.
- the organic halide compounds will typically break down during abrading and release a halogen acid or a gaseous halide compound.
- Examples of such materials include chlorinated waxes like tetrachloronaphthalene, pentachloronaphthalene; and polyvinyl chloride.
- halide salts include sodium chloride, potassium cryolite, sodium cryolite, ammonium cryolite, potassium tetrafluoroborate, sodium tetrafluoroborate, silicon fluorides, potassium chloride, magnesium chloride.
- metals include, tin, lead, bismuth, cobalt, antimony, cadmium, iron titanium.
- Other miscellaneous grinding aids include sulfur, organic sulfur compounds, graphite and metallic sulfides. It is also within the scope of this invention to use a combination of different grinding aids and in some instances this may produce a synergistic effect.
- the above mentioned examples of grinding aids is meant to be a representative showing of grinding aids, and it is not meant to encompass all grinding aids.
- Grinding aids may be used in abrasive slurries useful in the invention in amounts ranging from about 0.1 to about 10 dry weight percent, more preferably from about 0.5 to about 5.0 weight percent, based on total weight of slurry. If non-reactive fillers are employed they may be used up to 50 dry weight percent.
- Abrasive slurries useful in the invention may contain any number of conventional additives such as one or more additional components, such as, for example, plasticizer, chelating agent, pH modifier, defoamer, foaming agent, reinforcing polymer, anti-freeze agent, suspension aid, bactericide, fingicide, and/or thickener.
- additional components such as, for example, plasticizer, chelating agent, pH modifier, defoamer, foaming agent, reinforcing polymer, anti-freeze agent, suspension aid, bactericide, fingicide, and/or thickener.
- Abrasive slurries of the invention may be prepared by mixing abrasive particles having known particle size ranging from 5 micrometers and known particle size distribution ranging from 1-75 micrometers with deionized water, and optionally other materials, to achieve slurry density ranging from about 0.01 gm/cc to about 0 . 2 gm/cc.
- the slurry may be mixed for 20 minutes at 1200 rpm using a high shear mixer, and the mixer may be left on during use of the slurry, but at lower rpm, in order to maintain a well dispersed slurry.
- the abrasive slurry may be converted into an atomized spray using an atomizing head having a venturi, similar to that illustrated schematically in FIG. 1 .
- the atomizing head may be manufactured out of aluminum, and may have one or more slurry inlet orifices of diameter of about 1 cm, one or more air (atomizing fluid) inlet orifices of diameter of 1 cm, and one or more atomized slurry outlet orifices having a diameter of 2 cm.
- the abrasive slurry may be fed to the atomizing head through a flexible stainless steel tube, the abrasive slurry drawn into the atomizing head by air entering the atomizing head at a pressure of about 100 psig.
- the atomized slurry emerges from the atomizing head at a pressure of about 50 psig.
- the slurry tank may be maintained stirred as mentioned above.
- the slurry tank may be at atmospheric pressure and room temperature, although these conditions are simply convenient and not required.
- the atomized slurry may be directed at dielectric-coated surfaces of an etch chamber having deposits of silicon, silicon carbide, and other debris on the dielectric surface.
- the atomized slurry may be directed at the surfaces at a 90° angle, although other angles may be used.
- the pre-test roughness (Ra) of the dielectric surfaces are measured, as well as the post-test roughness after 30 seconds of contacting the atomized slurry to the dielectric surfaces.
- Ra is a common measure of roughness used in the abrasives industry. “Ra” is defined as the arithmetic mean of the departures of the roughness profile from the mean line. Ra may be measured with a profilometer probe, which has a diamond tipped stylus. In general, the lower the Ra value, the smoother or finer the workpiece surface finish. The profilometer known under the trade designation Perthen M4P may be used. Thickness of coatings may be determined by microsection techniques known in the art.
- Apparatus and methods of the present invention may to be used to effectively remove debris from surfaces of semiconductor etching chambers.
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Abstract
Description
- The invention is directed to cleaning apparatus and methods, particularly, but not limited to, apparatus and methods for cleaning products and chambers made during semiconductor manufacturing.
- Removal of contaminants from etch chamber components traditionally uses carbon dioxide pellet blasting, abrasive bead blasting, solvents, strong oxidizers, inorganic acids/bases or high temperature thermal decomposition. Depending on the contaminant/substrate combination, these produce marginal results in contaminant removal and providing high cleanliness surfaces for chamber reuse. These methods may also damage the substrate during the cleaning process particularly when using conventional mechanical cleaning methods for anodized and coated aluminum substrates. More recent designs of chamber components make use of plasma sprayed dielectric coatings such as Al2O3, ZrO2, and Y2O3. These coatings are applied to ceramic and anodized aluminum substrates where coating adhesion is marginal at best and are easily damaged during cleaning due to the aggressive nature of conventional abrasive blasting techniques.
- Clearly there is a real need for effective removal of deposits from all surfaces used during the process of creating a semiconductor wafer without degrading or damaging the substrate or coating surface.
- In accordance with the present invention, apparatus and methods are presented which overcome or reduce deficiencies associated with previous apparatus and methods in cleaning semiconductor etching chambers and components.
- A first aspect of the invention is an apparatus, one apparatus comprising:
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- (a) an atomizing head adapted to produce an atomized abrasive slurry, the head having an abrasive slurry inlet, an atomizing fluid inlet, and an atomized abrasive slurry outlet;
- (b) an abrasive slurry container fluidly connected to the abrasive slurry inlet and defining a space for a slurry comprising water and abrasive particles; and
- (c) a source of atomizing fluid fluidly connected to the atomizing fluid inlet.
- Apparatus within the invention include those wherein the container may have an agitator adapted to maintain the abrasive particles well dispersed. “Well dispersed”, as used herein, means that the abrasive slurry may be a homogenous mixture of all ingredients. The source of atomizing fluid may be selected from a membrane unit, an absorption unit, a cryogenic unit, a container of fluid, a compressor, a pipeline, a gas cabinet, and combinations thereof. The source of atomizing fluid may comprise a source of one or more inert gases and combinations thereof. The inert gas may be selected from any gas that would be considered inert for the cleaning process, including, but not limited to, nitrogen, argon, air, nitrogen enriched air, noble gases other than argon, and combinations thereof. The atomizing head may comprise a venturi. Apparatus may comprise a pressure regulator adapted to adjust pressure of the atomizing fluid entering the atomizing head. The pressure regulator may be adapted to adjust pressure of the atomized abrasive slurry exiting the atomizing head.
- Another aspect of the invention is a method of cleaning, one method comprising directing an atomized abrasive slurry onto at least some internal surfaces of a semiconductor etching chamber or chamber components. Methods of the invention include those wherein the directing comprises controlling pressure of the atomized abrasive slurry. The pressure may generally be controlled within a pressure ranging from about 25 to about 150 psig. Pressures higher than 150 psig may be used if necessary to remove debris and the underlying substrate is not damaged. The density of the atomized abrasive slurry may need to be reduced; pressures lower than 25 psig may not be able to provide the desired cleaning efficiency, but may be used if the density of the atomized abrasive slurry is increased. Methods of the invention include those methods wherein the directing step comprises controlling density of the atomized abrasive slurry. Several ways are available for controlling density of the atomized slurry, including adding more liquid to the abrasive slurry, reducing the amount and/or density of the abrasive particles in the abrasive slurry, reducing the density of the atomizing fluid and/or increasing its flow rate, and combinations of these. The density of the atomized abrasive slurry may be controlled within a density ranging from about 0.01 gm/cc to about 0.2 gm/cc. Other methods of the invention include controlling momentum of the atomized abrasive slurry exiting the atomizing head. Methods of the invention include controlling momentum of the atomized abrasive slurry at momentum ranging from about 100,000 gm-cm/sec to about 300,000 gm-cm/sec. Other methods may include maintaining the abrasive slurry in the abrasive slurry container in well dispersed state, and methods wherein the composition of the abrasive slurry in the container is controlled.
- The various aspects of the invention will become more apparent after review of the following brief description of the drawings, detailed description, and claims.
- The manner in which the objectives of the invention and other desirable characteristics can be obtained is explained in the following description and attached drawings in which:
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FIGS. 1 and 2 are schematic side elevation views of first and second apparatus embodiments according to the present invention. - It is to be noted, however, that the appended drawings are not to scale and illustrate only typical embodiments of this invention, and are therefore not to be considered limiting of its scope, for the invention may admit to other equally effective embodiments.
- In the following description, numerous details are set forth to provide an understanding of the present invention. However, it will be understood by those skilled in the art that the present invention may be practiced without these details and that numerous variations or modifications from the described embodiments may be possible.
- All phrases, derivations, collocations and multiword expressions used herein, in particular in the claims that follow, are expressly not limited to nouns and verbs. It is apparent that meanings are not just expressed by nouns and verbs or single words. Languages use a variety of ways to express content. The existence of inventive concepts and the ways in which these are expressed varies in language-cultures. For example, many lexicalized compounds in Germanic languages are often expressed as adjective-noun combinations, noun-preposition-noun combinations or derivations in Romanic languages. The possibility to include phrases, derivations and collocations in the claims is essential for high-quality patents, making it possible to reduce expressions to their conceptual content, and all possible conceptual combinations of words that are compatible with such content (either within a language or across languages) are intended to be included in the used phrases.
- In accordance with the present invention, apparatus and methods are presented which overcome or reduce problems associated with previous methods and apparatus. Apparatus of the invention comprise an atomizing head functioning to produce an atomized abrasive slurry. The head comprises an abrasive slurry inlet, an atomizing fluid inlet, and an atomized abrasive slurry outlet. The atomizing head may include any internal volume capable of producing an atomized abrasive slurry, including a venturi, a converging-diverging nozzle, a converging nozzle, and other nozzle configurations.
- In simplified terms there are three major methods for achieving atomization of a liquid or slurry:
- 1. rotating cup atomization involves shredding the fluid with the air of a moving mechanical element.
- 2. in mechanical atomization the fluid to be atomized is compressed to very high pressures (15 to 30 bars), thus imparting to it a high potential energy converted to kinetic energy when released to atmospheric pressure. This energy results in shearing of the liquid when it is brought into contact with the exterior atmosphere and thus results in the formation of droplets.
- 3. gaseous-fluid-assisted atomization can be used to arrive at a similar result while achieving a saving on high pressures (2 to 6 bars).
- Apparatus of the present invention are concerned with the third category of atomization. In simplified terms one can distinguish two types of gaseous-fluid-assisted atomization according to whether the liquid to be atomized and atomizing fluid are brought into contact inside or outside the atomizer head. These types may be referred to as internal atomization and external atomization. Both types are useful in the present invention.
- Internal atomization is characterized by confinement of the liquid and atomizing fluid in a contacting chamber. The mode of introduction of the two fluids into this chamber can vary considerably and has a direct influence on the characteristics of the atomized slurry that exits from the chamber. Likewise, the internal geometry of this chamber (overall volume, vanes for producing rotation, number and diameters of the inlet and outlet orifices, and so forth) also affects the specific characteristics of the liquid/atomizing fluid mixture. This mode of atomization generally affords an excellent quality of atomization, that is, an atomized slurry composed of very small slurry droplets with a very narrow droplet size distribution about these small diameters. At a given liquid delivery rate, this atomization quality is naturally a function of the atomizing fluid delivery rate employed and the pressure level prevailing in the interior of the atomizing chamber.
- For external atomization, where contact between the two phases takes place outside of any confining enclosure, the atomized slurry is created mainly by shearing of the jet of liquid slurry by the atomizing fluid. The geometry of the outlets for the two fluids completely determines the quality of the atomization, and droplet size analysis of the drops resulting from the contact may show a relatively wide diameter distribution (simultaneous-presence of small and large droplets).
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FIG. 1 is a schematic side elevation view of oneapparatus embodiment 100 according to the present invention, comprising an atomizing head 2 having an atomizing fluid inlet 4, an abrasive slurry inlet 6, and an atomized abrasive slurry outlet 8. Atomizing head 2 may be made from any suitable material or combination of materials, such as metal, plastic, and combinations thereof. Suitable metals include aluminum, stainless steels, such as 304 stainless steel. The stainless steel may be electropolished, but this is not a requirement of the invention. Inembodiment 100, the internal flow channels include a convergingnozzle 10, aparallel throat section 12, and a divergingnozzle 14.Throat 12 includes in this embodiment an inlet port ororifice 16 for abrasive slurry, which is drawn intothroat 12 by negative pressure caused by flowing fluidizing fluid. Abrasive slurry may be drawn up from one or moreabrasive slurry containers 20, and head 2 may have one or more fluid connections to one or more sources of fluidizingfluid 18. Although this particular flow configuration represents a venturi, the invention is not so limited. - There are numerous options in the design of each particular atomizing head, and all are considered foreseeable alternative embodiments within the present invention. For example, in head 2 of
FIG. 1 , atomizing fluid inlet may be comprised of one, two, or more than two inlet orifices, as mayabrasive inlet orifice 16. For example, it may be advantageous to place an inlet port or orifice 16 a opposite oforifice 16. -
FIG. 2 is a schematic side elevation view of anotherapparatus embodiment 200 according to the present invention, similar toembodiment 100 illustrated inFIG. 1 , comprising anatomizing head 22 having an atomizing fluid inlet 4, an abrasive slurry inlet 6, and an atomized abrasive slurry outlet 8. However inembodiment 200, the internal flow channels include a more streamlined converging-divergingnozzle throat 26.Throat 26 also includes in this embodiment an inlet port ororifice 16 for abrasive slurry, which is drawn intothroat 26 by negative pressure caused by flowing fluidizing fluid. Abrasive slurry may be drawn up from one or moreabrasive slurry containers 20, and head 2 may have one or more fluid connections to one or more sources of fluidizingfluid 18. - Another component of apparatus of the invention is an abrasive slurry container fluidly connected to the abrasive slurry inlet of the atomizing head. The container functions to define a space for a slurry comprising water, abrasive particles, and other optional ingredients, depending on the particular cleaning task, for example the type and quantity of debris or deposits to be removed, the underlying substrate composition and hardness, and the properties of any substrate coating, such as a refractory or dielectric coating.
- The abrasive slurry container may be under atmospheric pressure, at a slight vacuum, or at a pressure above atmospheric, although the pressure in the container is not critical. The container may be closed or open to the atmosphere. If the container is at a pressure less than or greater than atmospheric the container will necessarily be manufactured to withstand these conditions. The container may comprise an outer shell with a bladder arrangement, where abrasive slurry is held inside the bladder. Air or other fluid may be used to force slurry out of the bladder, and a vacuum may assist loading the bladder with the abrasive slurry.
- The configuration of the abrasive slurry container is not critical, as long the abrasive particles are able to be kept suspended, or reasonably so, in the container. There may be occasions when there are more abrasive particles than required for a particular task, in which case not all abrasives particles will need to be suspended. Some may be allowed to settle out to the bottom of the container until needed. The materials of construction of the slurry container are not critical. The container may be metal, plastic, or some combination thereof. A refractory or ceramic container may even be used, and a liner may be used. The liner may be a ceramic or plastic material. Suspension aids may be used. These may be chemical, mechanical or combination thereof. A mechanical suspension aide may comprise one or more stirring or agitating device. A chemical suspension aide may comprise one or more suspension aide chemicals. Examples of these latter are discussed further herein.
- Apparatus of the invention may comprise a source of atomizing fluid fluidly connected to the atomizing fluid inlet. The source of atomizing fluid is selected from a membrane unit, an absorption unit, a cryogenic unit, a container of fluid, a compressor, a pipeline, a gas cabinet, and combinations thereof. The source of atomizing fluid may comprise a source of one or more inert gases and combinations thereof. If used, the inert gas may be selected from sources of nitrogen, argon, air, nitrogen enriched air, noble gases other than argon, and combinations and mixtures thereof. The atomizing fluid need not be a pure gas. For example, the atomizing fluid may be air, or nitrogen generated by a membrane separation unit producing nitrogen enriched air. Most nitrogen membranes generate nitrogen having about 90 to 95 percent nitrogen, although higher purity is possible by using multiple membrane units connects in series or in cascade fashion. Purities of higher than 95 percent may not be necessary. The dryness of the gas used may be a concern, for if the atomizing fluid is a gas and the gas has considerable water or other liquid, the composition of the atomized abrasive slurry might be different from that in the abrasive slurry container, possibly resulting in inconsistent results. The source of atomizing fluid is fluidly connected to the atomizing head by one or more conduits, which may include one or more pressure regulators adapted to adjust pressure of the atomizing fluid as it enters the atomizing head. If the amount of abrasive slurry feed to the atomizing head is maintained relatively constant, the pressure regulator may be adapted to adjust pressure of the atomized abrasive slurry as well. The pressure of the source of atomizing fluid may be any pressure required to atomize a particular slurry and perform the cleaning function. The pressure of the source of atomizing fluid may be controlled, such as by use of a gas cabinet, or it may be taken from a pipeline where there is little control over the pressure of the atomizing fluid in the pipeline.
- In operation, methods of the invention include directing an atomized abrasive slurry onto at least some internal surfaces of a semiconductor etching chamber. The methods include generating the atomized abrasive slurry by flowing an atomizing fluid through an atomizing head, as described. Generating the atomized abrasive slurry may comprise controlling pressure of the atomized abrasive slurry exiting the atomizing head at a pressure ranging from about 25 to about 150 psig. The generating may comprise controlling density of the atomized abrasive slurry to a density ranging from about 0.01 gm/cc to about 0.2 gm/cc. It is desirous to control the momentum of the atomized abrasive slurry as it contacts the workpiece. The momentum of the atomized abrasive slurry at the workpiece may be controlled by controlling the momentum of the atomized abrasive slurry as it exits the atomizing head. The momentum of the atomized abrasive slurry exiting the atomizing head may be controlled with in a range of from about 100,000 gm-cm/sec to about 300,000 gm-cm/sec. The momentum of the atomized abrasive slurry as it exits the atomizing head may be controlled by adjusting the pressure of the atomizing fluid as it enters the atomizing head, the amount of slurry entering the atomizing head, the density of the abrasive slurry, or any combination of these.
- The abrasive slurry may be maintained in a well-dispersed state in the abrasive slurry container. As noted previously, in the context of the invention this means the abrasive slurry may be a homogenous mixture of all ingredients.
- Abrasive particles useful in the invention may be selected from those commonly used in the abrasive art, however, the abrasive particles (size and composition) will be chosen with the degree of surface roughness, coating thickness change, and adhesion properties in mind. In choosing an appropriate abrasive particle, characteristics such as hardness, compatibility with the intended workpiece, particle size, reactivity with the workpiece, as well as heat conductivity may be considered.
- The composition of abrasive particles useful in the invention can be divided into two classes: natural abrasives and manufactured abrasives. Examples of natural abrasives include: diamond, corundum, emery, garnet, buhrstone, chert, quartz, sandstone, chalcedony, flint, quartzite, silica, feldspar, pumice and talc. Examples of manufactured abrasives include: boron carbide, cubic boron nitride, fused alumina, ceramic aluminum oxide, heat treated aluminum oxide, alumina zirconia, glass, silicon carbide, iron oxides, tantalum carbide, cerium oxide, tin oxide, titanium carbide, synthetic diamond, manganese dioxide, zirconium oxide, and silicon nitride.
- Abrasive particles useful in the invention typically and preferably have a particle size ranging from about 0.1 micrometer to about 1500 micrometers, more preferably ranging from about 0.1 micrometer to about 1300 micrometers. The abrasive particles preferably have an average particle size ranging from about 0.1 micrometer to about 700 micrometers, more preferably ranging from about 1 to about 150 micrometers, particularly preferably from about 1 to about 80 micrometers. It is preferred that abrasive particles used in the invention have a Moh's hardness of at least 8, more preferably above 9; however, for specific applications, softer particles may be used.
- The term “abrasive particle” includes agglomerates of individual abrasive particles. An abrasive agglomerate is formed when a plurality of abrasive particles are bonded together with a binder to form a larger abrasive particle which may have a specific particulate structure. The plurality of particles which form the abrasive agglomerate may comprise more than one type of abrasive particle and a binder.
- Generally, fillers are inorganic particulate matter which comprise apparatus which are substantially inert or non-reactive with respect to the surface acted upon by the abrasive. Occasionally, however, active (i.e. reactive) fillers are used, sometimes referred to in the abrasives art as grinding aids. These fillers interact beneficially with the workpiece during use. In particular, it is believed in the art that the grinding aid may either 1) decrease the friction between the abrasive particles and the workpiece being abraded, 2) prevent the abrasive particle from “capping”, i.e. prevent metal particles from becoming welded to the tops of the abrasive particles, 3) decrease the interface temperature between the abrasive particles and the workpiece or 4) decrease the required grinding force.
- Grinding aids encompass a wide variety of different materials and can be inorganic or organic based. Examples of chemical groups of grinding aids useful in this invention include waxes, organic halide compounds, halide salts and metals and their alloys. The organic halide compounds will typically break down during abrading and release a halogen acid or a gaseous halide compound. Examples of such materials include chlorinated waxes like tetrachloronaphthalene, pentachloronaphthalene; and polyvinyl chloride. Examples of halide salts include sodium chloride, potassium cryolite, sodium cryolite, ammonium cryolite, potassium tetrafluoroborate, sodium tetrafluoroborate, silicon fluorides, potassium chloride, magnesium chloride. Examples of metals include, tin, lead, bismuth, cobalt, antimony, cadmium, iron titanium. Other miscellaneous grinding aids include sulfur, organic sulfur compounds, graphite and metallic sulfides. It is also within the scope of this invention to use a combination of different grinding aids and in some instances this may produce a synergistic effect. The above mentioned examples of grinding aids is meant to be a representative showing of grinding aids, and it is not meant to encompass all grinding aids.
- Grinding aids may be used in abrasive slurries useful in the invention in amounts ranging from about 0.1 to about 10 dry weight percent, more preferably from about 0.5 to about 5.0 weight percent, based on total weight of slurry. If non-reactive fillers are employed they may be used up to 50 dry weight percent.
- Abrasive slurries useful in the invention may contain any number of conventional additives such as one or more additional components, such as, for example, plasticizer, chelating agent, pH modifier, defoamer, foaming agent, reinforcing polymer, anti-freeze agent, suspension aid, bactericide, fingicide, and/or thickener.
- Abrasive slurries of the invention may be prepared by mixing abrasive particles having known particle size ranging from 5 micrometers and known particle size distribution ranging from 1-75 micrometers with deionized water, and optionally other materials, to achieve slurry density ranging from about 0.01 gm/cc to about 0.2 gm/cc. The slurry may be mixed for 20 minutes at 1200 rpm using a high shear mixer, and the mixer may be left on during use of the slurry, but at lower rpm, in order to maintain a well dispersed slurry.
- The abrasive slurry may be converted into an atomized spray using an atomizing head having a venturi, similar to that illustrated schematically in
FIG. 1 . As an example, the atomizing head may be manufactured out of aluminum, and may have one or more slurry inlet orifices of diameter of about 1 cm, one or more air (atomizing fluid) inlet orifices of diameter of 1 cm, and one or more atomized slurry outlet orifices having a diameter of 2 cm. The abrasive slurry may be fed to the atomizing head through a flexible stainless steel tube, the abrasive slurry drawn into the atomizing head by air entering the atomizing head at a pressure of about 100 psig. The atomized slurry emerges from the atomizing head at a pressure of about 50 psig. The slurry tank may be maintained stirred as mentioned above. The slurry tank may be at atmospheric pressure and room temperature, although these conditions are simply convenient and not required. The atomized slurry may be directed at dielectric-coated surfaces of an etch chamber having deposits of silicon, silicon carbide, and other debris on the dielectric surface. The atomized slurry may be directed at the surfaces at a 90° angle, although other angles may be used. The pre-test roughness (Ra) of the dielectric surfaces are measured, as well as the post-test roughness after 30 seconds of contacting the atomized slurry to the dielectric surfaces. “Ra” is a common measure of roughness used in the abrasives industry. “Ra” is defined as the arithmetic mean of the departures of the roughness profile from the mean line. Ra may be measured with a profilometer probe, which has a diamond tipped stylus. In general, the lower the Ra value, the smoother or finer the workpiece surface finish. The profilometer known under the trade designation Perthen M4P may be used. Thickness of coatings may be determined by microsection techniques known in the art. - Apparatus and methods of the present invention may to be used to effectively remove debris from surfaces of semiconductor etching chambers. Although only a few exemplary embodiments of this invention have been described in detail above, those skilled in the art will readily appreciate that many modifications are possible in the exemplary embodiments without materially departing from the novel teachings and advantages of this invention. Accordingly, all such modifications are intended to be included within the scope of this invention as defined in the following claims.
Claims (20)
Priority Applications (10)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/272,844 US20070111642A1 (en) | 2005-11-14 | 2005-11-14 | Apparatus and methods for slurry cleaning of etch chambers |
DE602006013768T DE602006013768D1 (en) | 2005-11-14 | 2006-10-31 | Process for cleaning etch chambers with abrasive suspension |
IL178946A IL178946A (en) | 2005-11-14 | 2006-10-31 | Apparatus and methods for slurry cleaning of etch chambers |
EP06255599A EP1785230B1 (en) | 2005-11-14 | 2006-10-31 | Method for slurry cleaning of etch chambers |
AT06255599T ATE464978T1 (en) | 2005-11-14 | 2006-10-31 | METHOD FOR CLEANING ETCHING CHAMBERS WITH GRINDING SUSPENSION |
SG200607533-7A SG132602A1 (en) | 2005-11-14 | 2006-11-02 | Apparatus and methods for slurry cleaning of etch chambers |
CNA2006101464827A CN1970230A (en) | 2005-11-14 | 2006-11-13 | Apparatus and methods for slurry cleaning of etch chambers |
KR1020060111696A KR101301097B1 (en) | 2005-11-14 | 2006-11-13 | Apparatus and methods for slurry cleaning of etch chambers |
TW095141986A TWI421935B (en) | 2005-11-14 | 2006-11-14 | Apparatus and methods for slurry cleaning of etch chambers |
JP2006307392A JP5031329B2 (en) | 2005-11-14 | 2006-11-14 | Apparatus and method for slurry cleaning an etch chamber |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/272,844 US20070111642A1 (en) | 2005-11-14 | 2005-11-14 | Apparatus and methods for slurry cleaning of etch chambers |
Publications (1)
Publication Number | Publication Date |
---|---|
US20070111642A1 true US20070111642A1 (en) | 2007-05-17 |
Family
ID=37758692
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/272,844 Abandoned US20070111642A1 (en) | 2005-11-14 | 2005-11-14 | Apparatus and methods for slurry cleaning of etch chambers |
Country Status (10)
Country | Link |
---|---|
US (1) | US20070111642A1 (en) |
EP (1) | EP1785230B1 (en) |
JP (1) | JP5031329B2 (en) |
KR (1) | KR101301097B1 (en) |
CN (1) | CN1970230A (en) |
AT (1) | ATE464978T1 (en) |
DE (1) | DE602006013768D1 (en) |
IL (1) | IL178946A (en) |
SG (1) | SG132602A1 (en) |
TW (1) | TWI421935B (en) |
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US20140094093A1 (en) * | 2012-09-25 | 2014-04-03 | Paul L. Miller | Underwater Abrasive Entrainment Waterjet Cutting |
WO2016176108A1 (en) * | 2015-04-30 | 2016-11-03 | Frito-Lay North America, Inc. | Method and apparatus for removing a portion of a food product with an abrasive stream |
US20170151651A1 (en) * | 2012-09-25 | 2017-06-01 | Paul L. Miller | Abrasive Entrainment Waterjet Cutting |
US20170151650A1 (en) * | 2012-09-25 | 2017-06-01 | Paul L. Miller | Abrasive Entrainment Waterjet Cutting |
US9687953B2 (en) | 2014-06-27 | 2017-06-27 | Applied Materials, Inc. | Chamber components with polished internal apertures |
US20180043505A1 (en) * | 2016-08-15 | 2018-02-15 | Paul L. Miller | Abrasive Entrainment Waterjet Cutting |
US20180080734A1 (en) * | 2016-08-15 | 2018-03-22 | Paul L. Miller | Abrasive Entrainment Waterjet Cutting |
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KR101091132B1 (en) | 2010-09-27 | 2011-12-09 | (주)제이솔루션 | Nitrogen gas ejection apparatus |
CN105904330A (en) * | 2016-06-08 | 2016-08-31 | 重庆巨源不锈钢制品有限公司 | Automatic polishing device and method |
CN109210374B (en) * | 2017-06-30 | 2021-06-08 | 北京北方华创微电子装备有限公司 | Air inlet pipeline and semiconductor processing equipment |
KR102577058B1 (en) * | 2021-04-30 | 2023-09-11 | 남근식 | Water-jet processing apparatus for grainding surface |
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Also Published As
Publication number | Publication date |
---|---|
CN1970230A (en) | 2007-05-30 |
SG132602A1 (en) | 2007-06-28 |
TWI421935B (en) | 2014-01-01 |
EP1785230A3 (en) | 2007-07-18 |
DE602006013768D1 (en) | 2010-06-02 |
KR20070051707A (en) | 2007-05-18 |
EP1785230A2 (en) | 2007-05-16 |
EP1785230B1 (en) | 2010-04-21 |
JP2007173785A (en) | 2007-07-05 |
TW200725733A (en) | 2007-07-01 |
IL178946A0 (en) | 2007-03-08 |
IL178946A (en) | 2012-10-31 |
ATE464978T1 (en) | 2010-05-15 |
JP5031329B2 (en) | 2012-09-19 |
KR101301097B1 (en) | 2013-08-27 |
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