US20070099428A1 - Plasma for patterning advanced gate stacks - Google Patents

Plasma for patterning advanced gate stacks Download PDF

Info

Publication number
US20070099428A1
US20070099428A1 US11/544,351 US54435106A US2007099428A1 US 20070099428 A1 US20070099428 A1 US 20070099428A1 US 54435106 A US54435106 A US 54435106A US 2007099428 A1 US2007099428 A1 US 2007099428A1
Authority
US
United States
Prior art keywords
plasma
nitrogen
composition
stack
boron
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
Application number
US11/544,351
Inventor
Denis Shamiryan
Vasile Paraschiv
Marc Demand
Werner Boullart
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Interuniversitair Microelektronica Centrum vzw IMEC
Original Assignee
Interuniversitair Microelektronica Centrum vzw IMEC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Interuniversitair Microelektronica Centrum vzw IMEC filed Critical Interuniversitair Microelektronica Centrum vzw IMEC
Priority to US11/544,351 priority Critical patent/US20070099428A1/en
Assigned to INTERUNIVERSITAIR MICROELEKTRONICA CENTRUM (IMEC) reassignment INTERUNIVERSITAIR MICROELEKTRONICA CENTRUM (IMEC) ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: PARASCHIV, VASILE, SHAMIRYAN, DENIS, BOULLART, WERNER, DEMAND, MARC
Publication of US20070099428A1 publication Critical patent/US20070099428A1/en
Assigned to IMEC reassignment IMEC "IMEC" IS AN ALTERNATIVE OFFICIAL NAME FOR "INTERUNIVERSITAIR MICROELEKTRONICA CENTRUM VZW" Assignors: INTERUNIVERSITAIR MICROELEKTRONICA CENTRUM VZW
Abandoned legal-status Critical Current

Links

Images

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/04Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer
    • H01L21/18Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic System or AIIIBV compounds with or without impurities, e.g. doping materials
    • H01L21/30Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
    • H01L21/31Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
    • H01L21/3205Deposition of non-insulating-, e.g. conductive- or resistive-, layers on insulating layers; After-treatment of these layers
    • H01L21/321After treatment
    • H01L21/3213Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer
    • H01L21/32133Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer by chemical means only
    • H01L21/32135Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer by chemical means only by vapour etching only
    • H01L21/32136Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer by chemical means only by vapour etching only using plasmas
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/04Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer
    • H01L21/18Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic System or AIIIBV compounds with or without impurities, e.g. doping materials
    • H01L21/28Manufacture of electrodes on semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/268
    • H01L21/28008Making conductor-insulator-semiconductor electrodes
    • H01L21/28017Making conductor-insulator-semiconductor electrodes the insulator being formed after the semiconductor body, the semiconductor being silicon
    • H01L21/28026Making conductor-insulator-semiconductor electrodes the insulator being formed after the semiconductor body, the semiconductor being silicon characterised by the conductor
    • H01L21/2807Making conductor-insulator-semiconductor electrodes the insulator being formed after the semiconductor body, the semiconductor being silicon characterised by the conductor the final conductor layer next to the insulator being Si or Ge or C and their alloys except Si
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/04Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer
    • H01L21/18Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic System or AIIIBV compounds with or without impurities, e.g. doping materials
    • H01L21/28Manufacture of electrodes on semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/268
    • H01L21/28008Making conductor-insulator-semiconductor electrodes
    • H01L21/28017Making conductor-insulator-semiconductor electrodes the insulator being formed after the semiconductor body, the semiconductor being silicon
    • H01L21/28026Making conductor-insulator-semiconductor electrodes the insulator being formed after the semiconductor body, the semiconductor being silicon characterised by the conductor
    • H01L21/28088Making conductor-insulator-semiconductor electrodes the insulator being formed after the semiconductor body, the semiconductor being silicon characterised by the conductor the final conductor layer next to the insulator being a composite, e.g. TiN
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/04Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer
    • H01L21/18Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic System or AIIIBV compounds with or without impurities, e.g. doping materials
    • H01L21/30Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
    • H01L21/31Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
    • H01L21/3105After-treatment
    • H01L21/311Etching the insulating layers by chemical or physical means
    • H01L21/31105Etching inorganic layers
    • H01L21/31111Etching inorganic layers by chemical means
    • H01L21/31116Etching inorganic layers by chemical means by dry-etching
    • H01L21/31122Etching inorganic layers by chemical means by dry-etching of layers not containing Si, e.g. PZT, Al2O3
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L29/00Semiconductor devices adapted for rectifying, amplifying, oscillating or switching, or capacitors or resistors with at least one potential-jump barrier or surface barrier, e.g. PN junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof  ; Multistep manufacturing processes therefor
    • H01L29/40Electrodes ; Multistep manufacturing processes therefor
    • H01L29/43Electrodes ; Multistep manufacturing processes therefor characterised by the materials of which they are formed
    • H01L29/49Metal-insulator-semiconductor electrodes, e.g. gates of MOSFET
    • H01L29/51Insulating materials associated therewith
    • H01L29/511Insulating materials associated therewith with a compositional variation, e.g. multilayer structures
    • H01L29/513Insulating materials associated therewith with a compositional variation, e.g. multilayer structures the variation being perpendicular to the channel plane
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L29/00Semiconductor devices adapted for rectifying, amplifying, oscillating or switching, or capacitors or resistors with at least one potential-jump barrier or surface barrier, e.g. PN junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof  ; Multistep manufacturing processes therefor
    • H01L29/40Electrodes ; Multistep manufacturing processes therefor
    • H01L29/43Electrodes ; Multistep manufacturing processes therefor characterised by the materials of which they are formed
    • H01L29/49Metal-insulator-semiconductor electrodes, e.g. gates of MOSFET
    • H01L29/51Insulating materials associated therewith
    • H01L29/517Insulating materials associated therewith the insulating material comprising a metallic compound, e.g. metal oxide, metal silicate
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L29/00Semiconductor devices adapted for rectifying, amplifying, oscillating or switching, or capacitors or resistors with at least one potential-jump barrier or surface barrier, e.g. PN junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof  ; Multistep manufacturing processes therefor
    • H01L29/66Types of semiconductor device ; Multistep manufacturing processes therefor
    • H01L29/68Types of semiconductor device ; Multistep manufacturing processes therefor controllable by only the electric current supplied, or only the electric potential applied, to an electrode which does not carry the current to be rectified, amplified or switched
    • H01L29/76Unipolar devices, e.g. field effect transistors
    • H01L29/772Field effect transistors
    • H01L29/78Field effect transistors with field effect produced by an insulated gate

Definitions

  • a method of dry etching of advanced gate stacks is provided which can be used to etch metal gate comprising stacks and pure germanium comprising stacks.
  • An etch plasma composition is also provided for dry etching of metal gate comprising stacks and pure germanium comprising stacks, thereby preserving the vertical profile of the gate stack after patterning.
  • Etching of metal gates has been studied addressing metal gate and gate oxide surface roughness, CD control, etch selectivity, and low damage etching but none of them succeeded in preserving the vertical profile of the gate stack after patterning.
  • BCl 3 One of the promising chemistry for patterning of advanced gate stacks (metal gate etch or high-k removal) is BCl 3 .
  • the main advantage of this plasma is that it can etch both metal gates and high-k dielectric with reasonable selectivity to the Si substrate.
  • Two particular examples are Ge gates and TaN metal gates. If a pure BCl 3 plasma is applied during the patterning of the gate stacks containing Ge or TaN a profile distortion caused by lateral etch is observed.
  • a dry-etch plasma composition for preserving the vertical profile of a structure comprising a stack of layers during anisotropical dry-etch patterning is provided.
  • Said plasma composition is further characterized such that during the dry-etch patterning of said stack a water-soluble film, which is removable against the structure, is deposited onto the sidewalls of said stack such that lateral attack of said patterned stack is avoided.
  • the plasma composition of preferred embodiments is characterized as a plasma comprising a boron-halogen compound and nitrogen and wherein the ratio of the boron-halogen compound to nitrogen is from 19:1 up to 9:1. More preferred, the plasma composition of the preferred embodiments is characterized as a plasma composition wherein said plasma comprises a boron-halogen compound, nitrogen and optionally an inert compound. Most preferred said boron-halogen compound is BCl 3 .
  • the plasma composition of the preferred embodiments is characterized as a plasma comprising (or consisting of) a boron-halogen compound and 5 up to 10% nitrogen (of the total plasma composition).
  • the plasma composition comprises (or consists of) a boron-halogen compound and less than 10% nitrogen (of the total plasma composition). More particularly, said boron-halogen compound is BCl 3 .
  • said plasma is (i.e. consists of) a BCl 3 plasma further comprising (or to which is added) from 5% to 10% nitrogen (based on the total plasma composition).
  • the stack of layers to be patterned is a metal gate comprising stack.
  • said metal gate comprising stack comprises at least one TaN layer or combinations of a TaN layer and a TiN layer (referred to as TaN/TiN metal gates) wherein said TaN layer is too sensitive to a (pure) BCl 3 plasma.
  • the stack of layers to be patterned is a stack wherein at least one layer of said stack of layers is a TaN layer.
  • At least one layer of said stack of layers to be patterned is a germanium comprising layer.
  • Said germanium layer can be situated upon a layer to be patterned by the plasma composition.
  • Said germanium layer can be a pure Ge layer.
  • the plasma of the preferred embodiments (during patterning) has a substrate bias which is different from zero.
  • the plasma of the preferred embodiments has a plasma power of from 100 W up to 1200 W. More preferred said plasma power is about 450 W.
  • the plasma of the preferred embodiments has a pressure in the plasma chamber of minimum 0.666 Pa (5 mT) and maximum 10.665 Pa (80 mT). More preferred said pressure is 0.666 Pa (5 mT).
  • the plasma of the preferred embodiments has a temperature below 100° C. and most preferred said plasma temperature during dry-etch patterning is about 60° C.
  • An anisotropical dry etching method is also provided using the plasma composition of the preferred embodiments as described above for patterning a stack of layers to create a vertical structure wherein lateral attack during patterning of said stack is avoided.
  • said method comprises the steps of first applying a dry-etch step using the plasma composition of the preferred embodiments wherein during the etching a protective and water-soluble film is deposited onto the vertical sidewalls of said structure such that the vertical profile of said structure is preserved and lateral attack is avoided. In a next step said water-soluble film is removed from said structure.
  • Said water-soluble film is preferably removed using a wet removal process using water.
  • a plasma comprising (or consisting of) BCl 3 , to which nitrogen is added to reach 5% to 10% of the total volume of the resulting plasma composition, for etching a (suitable) stack of layer (i.e. comprising at least one layer etchable by said BCl 3 component) and simultaneously passivating (or protecting) the sidewalls of said stack of layers from lateral etch.
  • a method for etching (or patterning) a (suitable) stack of layers while/and simultaneously passivating (or protecting) the sidewalls of said stack of layers comprising the step of providing a plasma comprising (or consisting of) BCl 3 , to which nitrogen is added to reach 5% to 10% of the total volume of the resulting plasma composition.
  • Said use or said method is particularly useful for (patterning) a stack of layers wherein at least one layer is germanium, or at least one layer is TaN.
  • Said passivating (or protecting) effect results from the formation and deposition of a film (or layer) which contains boron and nitrogen (and further compounds such as oxygen) on the sidewalls of said stack of layers.
  • Said film obtainable by a method of the preferred embodiments is also provided.
  • FIG. 1 shows FTIR (Fourier Transform Infrared Spectroscopy) spectra of films deposited from BCl 3 /N 2 plasma mixture (70% BCl 3 ) at 275° C. and 60° C.
  • FIG. 2 shows a Ge gate profile after the gate patterning and before the high-k removal.
  • FIG. 3 shows a Ge gate profile after high-k removal by pure BCl 3 plasma for 10 seconds ( FIG. 3A ) and BCl 3 /N 2 (10% N 2 ) plasma for 20 seconds ( FIG. 3B )
  • FIG. 4 shows a TaN gate profile after etching in pure BCl 3 plasma ( FIG. 4A ), an arrow indicates the lateral attack of TaN.
  • FIG. 4B shows a TaN gate profile after etching in BCl 3 /N 2 (5% N 2 ) plasma.
  • FIG. 5 shows a TaN gate profile after etching in BCl 3 /N 2 plasma ( FIG. 5A ) and a TaN gate profile after etching in BCl 3 /O 2 plasma ( FIG. 5B ).
  • critical dimension is a broad term, and is to be given its ordinary and customary meaning to a person of ordinary skill in the art (and is not to be limited to a special or customized meaning), and refers without limitation to the smallest dimensions of geometrical features (e.g. width of gate electrode) which can be formed during semiconductor device manufacturing.
  • bias as used herein is a broad term, and is to be given its ordinary and customary meaning to a person of ordinary skill in the art (and is not to be limited to a special or customized meaning), and refers without limitation to the voltage applied to the substrate during patterning in a dry etch chamber.
  • selectivity is a broad term, and is to be given its ordinary and customary meaning to a person of ordinary skill in the art (and is not to be limited to a special or customized meaning), and refers without limitation to the etch rate of a selected material towards another material.
  • the material to be etched away should have a much higher etch rate than the other materials.
  • ratio is a broad term, and is to be given its ordinary and customary meaning to a person of ordinary skill in the art (and is not to be limited to a special or customized meaning), and refers without limitation to an expression of an amount of a first compound to a second compound, e.g. a ratio of 9:1 means e.g. 9 sccm (standard centimeter cube per minute) of the first compound and 1 sccm of the second compound.
  • the preferred embodiments are further related to the patterning of a stack of layers, more specifically to the dry etching of a stack of layers.
  • Said patterning is making use of a plasma etch compound wherein at least one of the layers is too sensitive to said etch compound.
  • a protective layer onto the stack of layers such that said stack is protected for e.g. sidewall damage.
  • Said protective layer is deposited during the patterning (dry etching). Furthermore said protective layer is sacrificial and hence easy removable.
  • the “sacrificial” layer also referred to as “protective” layer or “passivation” layer refers to the BxNy like film resulting from the addition of nitrogen in the boron-halogen plasma, also referred to as BxNy film or as to boron nitride like film, which is deposited during etching.
  • Said BxNy film is used as a “protective” or “passivating” film during patterning/etching of a structure, said BxNy film is also referred to as a sacrificial layer because said layer is removed after patterning is completed. Due the unstable character of the BxNy film and water soluble character said BxNy film can be easily removed by e.g. a water rinse.
  • BxNy film refers to a film comprising mainly boron and nitrogen which is further characterized as a water-soluble film.
  • the BxNy film of the preferred embodiments is water soluble, in contrast to a pure BN which is insoluble in water.
  • the BxNy film contains hexagonal boron nitride, but is very unlikely to be a stoichiometric BN.
  • the BxNy film is therefore referred to as BxNy wherein the integers x and y indicate that the ratio of nitrogen and boron in the film is not fixed due to the presence of other compounds (impurities) in the film such as water, oxygen and/or ammonia which are possibly absorbed from the plasma and/or atmosphere after dry-etching.
  • the preferred embodiments relate to the patterning of metal gate stacks or germanium gate stacks, more specifically it relates to the dry etching of said gate stacks such as TaN comprising metal gate stacks and to the dry etching of Ge comprising stacks (or in other words a stack comprising e.g. a pure Ge layer).
  • the methods and compositions of preferred embodiments can solve or minimize the problem of lateral etch and profile attack during the patterning of advanced gate stacks such as metal gate stacks and germanium stacks by adding small amounts of nitrogen to a boron-halogen plasma such as BCl 3 plasma in order to improve gate profile control.
  • a boron-halogen plasma such as BCl 3 plasma
  • the mixture of BCl 3 /N 2 plasma results in a deposition of BxNy-like film that inhibits the lateral etch but does not inhibit vertical etch as the formed BxNy-like film is destroyed by ion bombardment.
  • a plasma composition is provided for patterning metal gate stacks and/or germanium stacks wherein during the patterning of said stack a protective and water-soluble film is deposited such that the vertical profile of the stack is preserved and lateral attack of said stack is avoided.
  • a plasma composition for patterning a stack of layers wherein at least one layer of said stack is sensitive to one of the etch compounds.
  • the plasma composition is preferably a Boron-halogen comprising plasma with small additions of nitrogen.
  • the Boron-halogen compound is preferably BCl 3 and said small additions of nitrogen are such that the ratio of the boron-halogen compound to nitrogen is from 19:1 up to 9:1.
  • an inert compound can be added to the plasma comprising boron-halogen and nitrogen.
  • Said inert compound can be e.g. argon or helium (He) and these compounds can be added to the plasma in concentrations up to 50% of the total plasma composition.
  • addition of inert compounds meaning that these compounds do not react with the substrate to be etched such that volatile compounds are formed
  • the inert compound can be seen as a catalyst.
  • the ratio of the boron-halogen compound to nitrogen is below 9:1 (having more boron-halogen), more preferred said ratio of the boron-halogen compound to nitrogen is below 11:1 and most preferred said ratio of the boron-halogen compound to nitrogen is 19:1.
  • the ratio of BCl 3 to nitrogen is below 9:1, more preferred said ratio of BCl 3 to nitrogen is below 11:1 and most preferred said ratio of BCl 3 to nitrogen is 19:1.
  • the ratio of the boron-halogen compound to nitrogen is higher than 19:1. More preferred said ratio of the boron-halogen compound to nitrogen is higher than 11:1 and most preferred the ratio of the boron-halogen compound to nitrogen is 9:1.
  • the ratio of BCl 3 to nitrogen is higher than 19:1. More preferred said ratio of BCl 3 to nitrogen is higher than 11:1 and most preferred the ratio of BCl 3 to nitrogen is 9:1.
  • the plasma composition is preferably a plasma comprising (or consisting of) a Boron-halogen compound and nitrogen, or in other words small additions of nitrogen in a boron-halogen plasma.
  • the plasma comprises (or consists of) a boron-halogen compound and 5% up to 10% nitrogen (of the total plasma composition).
  • the plasma composition comprises (or consists of) a boron-halogen compound and less than 10% nitrogen (of the total plasma composition) and most preferred said boron-halogen is BCl 3 .
  • the amount of N 2 to the total BCl 3 /N 2 plasma composition is higher than 5%, more preferred said amount of N 2 is higher than 8% N 2 to the total BCl 3 /N 2 plasma composition and most preferred said amount of N 2 is 10% to the total BCl 3 /N 2 plasma composition.
  • the amount of N 2 to the total BCl 3 /N 2 plasma composition is lower than 10%, more preferred said amount of N 2 is lower than 8% N 2 to the total BCl 3 /N 2 plasma composition and most preferred said amount of N 2 is 5% to the total BCl 3 /N 2 plasma composition.
  • the plasma of the preferred embodiments has a substrate bias which is different from zero.
  • the plasma of the preferred embodiments has a plasma power is from 100 W up to 1200 W. More preferred said plasma power is about 450 W.
  • the plasma of the preferred embodiments has a pressure in the plasma chamber of minimum 0.666 Pa (5 mT) and maximum 10.665 Pa (80 mT). More preferred said pressure is 0.666 Pa (5 mT).
  • the plasma of the preferred embodiments has a temperature below 100° C. and most preferred said plasma temperature during dry-etch patterning is about 60° C.
  • a boron-nitrogen (B x N y or BN) film deposited at higher temperatures is equal to a higher quality film containing less (or no) impurities which is more difficult or even not possible to remove.
  • non-Si comprising gate stacks are preferably metal gate comprising gate stacks such as TaN comprising gate stacks and preferably metal gate stacks comprising a (pure) germanium layer.
  • the dry-etching method of the preferred embodiments uses a plasma composition wherein at least one layer of said stack is too sensitive to one of the etch compounds.
  • Said dry etching method is characterized in that the vertical profile of said gate stack is preserved after etching.
  • the method of the preferred embodiments solves or minimizes the problem of negatively sloped gate profiles after dry etching by depositing a sacrificial layer during the etching.
  • Said sacrificial layer serves as a passivating layer during dry etching such that the vertical profile or CD of the gate stack is preserved.
  • the dry-etching method of the preferred embodiments solves or minimizes the problem of lateral etch and profile attack during the patterning of advanced gate stacks such as metal gate stacks and germanium comprising stacks by adding small amounts of nitrogen to a boron-halogen plasma such as BCl 3 plasma in order to improve gate profile control.
  • a boron-halogen plasma such as BCl 3 plasma
  • the mixture of BCl 3 /N 2 plasma results in a deposition of BxNy-like film that inhibits the lateral etch but does not inhibit vertical etch as the formed BxNy-like film is destroyed by ion bombardment.
  • the method of the preferred embodiments comprises the steps of first applying a dry-etch step using the plasma composition of the preferred embodiments whereby during the etching a protective and water-soluble film is deposited onto the vertical sidewalls of said structure such that the vertical profile of said structure is preserved and lateral attack is avoided. In a next step said water-soluble film is removed from said structure.
  • Said water-soluble film is preferably removed using a wet removal process, most preferred said wet removal is using water.
  • the dry-etching method of the preferred embodiments uses a boron-halogen comprising plasma with small additions of nitrogen.
  • the Boron-halogen compound is preferably BCl 3 and said small additions of nitrogen are such that the ratio of the boron-halogen compound to nitrogen is from 19:1 up to 9:1.
  • an inert compound can be added to the plasma comprising boron-halogen and nitrogen.
  • Said inert compound can be e.g. argon or helium (He) and these compounds can be added to the plasma in concentrations up to 50% of the total plasma composition.
  • the ratio of the boron-halogen compound to nitrogen is preferably below 9:1. More preferably, said ratio of the boron-halogen compound to nitrogen is below 11:1 and most preferred said ratio of the boron-halogen compound to nitrogen is 19:1.
  • said boron-halogen compound is BCl 3 .
  • the ratio of the boron-halogen compound to nitrogen is preferably higher than 19:1. More preferred said ratio of the boron-halogen compound to nitrogen is higher than 11:1 and most preferred the ratio of the boron-halogen compound to nitrogen is 9:1.
  • said boron-halogen compound is BCl 3 .
  • the plasma composition used in a method of the preferred embodiments is a plasma comprising (or consisting of) a Boron-halogen compound and nitrogen, or in other words small additions of nitrogen in a boron-halogen plasma.
  • the plasma comprises (or consists of) a boron-halogen compound and 5% up to 10% nitrogen (of the total plasma composition).
  • the plasma composition comprises (or consists of) a boron-halogen compound and less than 10% nitrogen (of the total plasma composition) and most preferred said boron-halogen is BCl 3 .
  • the amount of N 2 to the total BCl 3 /N 2 plasma composition is higher than 5%, more preferred said amount of N 2 is higher than 8% N 2 to the total BCl 3 /N 2 plasma composition and most preferred said amount of N 2 is 10% to the total BCl 3 /N 2 plasma composition.
  • the amount of N 2 to the total BCl 3 /N 2 plasma composition is lower than 10%, more preferred said amount of N 2 is lower than 8% N 2 to the total BCl 3 /N 2 plasma composition and most preferred said amount of N 2 is 5% to the total BCl 3 /N 2 plasma composition.
  • the plasma used in a method of the preferred embodiments has a substrate bias which is different from zero.
  • said plasma has a plasma power of 100 W up to 1200 W. More preferred said plasma power is about 450 W.
  • said plasma has a pressure in the plasma chamber of minimum 0.666 Pa (5 mT) and maximum 10.665 Pa (80 mT). More preferred said pressure is 0.666 Pa (5 mT).
  • said plasma has a temperature below 100° C. and more preferred said plasma temperature during dry-etch patterning is about 60° C.
  • boron-nitrogen (B x N y or BN) film deposited at higher temperatures is equal to a higher quality film containing less (or no) impurities, which is more difficult or even not possible to remove.
  • a method for the dry etching of non-Si comprising gate stacks is provided, said non-Si comprising gate stacks are preferably metal gate comprising gate stacks such as TaN comprising gate stacks and preferably pure germanium comprising metal stacks.
  • Said dry etching method is characterized in that the vertical profile of said gate stack is preserved after etching.
  • the method of the preferred embodiments solves the problem of negatively sloped gate profiles after dry etching by depositing a sacrificial layer during the etching.
  • Said sacrificial layer serves as a passivating layer during dry etching such that the vertical profile or CD of the gate stack is preserved.
  • a composition is provided of a plasma used to etch materials that are too sensitive to Cl-based plasmas. If those materials are etched with pure Cl-based plasmas such as BCl 3 plasmas, the etch profiles are distorted because these materials are etched in the lateral direction as well.
  • said materials are metal gate comprising gate stacks such as TaN comprising gate stacks and pure germanium comprising metal stacks.
  • the plasma of the preferred embodiments solves or minimizes the problem of damage caused by Cl-based plasmas, more specifically this is achieved by adding small amounts of nitrogen to the Cl-based plasma.
  • said Cl compound is preferably BCl 3 .
  • the amount of nitrogen added to the plasma is preferably from 5% up to 10%.
  • the addition of nitrogen to a Cl-based plasma such as BCl 3 preserves the vertical profile through the formation of a passivating B x N y -like layer on the vertical surfaces.
  • a Cl-based plasma with small additions of nitrogen for the patterning of non-Si based stacks is also provided.
  • Said patterning is further characterized as a patterning which avoids lateral etching and preserves the vertical profile.
  • Said stacks are preferably metal gate comprising gate stacks such as TaN comprising gate stacks and preferably pure germanium comprising metal stacks.
  • said Cl compound is BCl 3 .
  • the method of the preferred embodiments as well as the plasma and its use can be applied to any material that can be etched by Cl-based plasma but is too chemically reactive and has significant lateral etch component. Said lateral etch can be blocked by a BxNy-like passivation film deposited onto the vertical sidewalls while at the meanwhile the vertical etch is not significantly affected.
  • the BCl 3 /N 2 plasma was applied for patterning of two different stacks as described in Example 1 and 2: pure Ge gates and TaN metal gates in the TiN/TaN gate stack. In both cases, the lateral attack of the gate material was prevented by addition of small amount of N 2 (5%-10%) to the BCl 3 plasma. Furthermore the plasma settings were optimized and illustrated in Example 3.
  • the deposited (passivation) BxNy-like layer of the preferred embodiments is characterized by FTIR and illustrated in Example 4.
  • the BCl 3 /N 2 plasma was used to etch TaN metal gates, in the example presented here said TaN metal gate is present in a TiN/TaN gate stack where 15 nm TaN is in the contact with the gate dielectric and 70 nm TiN covers the TaN or in other words 70 nm TiN is situated on top of said 15 nm TaN.
  • the most critical step is TaN etching after TiN patterning.
  • BCl 3 plasma is used here for the TaN patterning as it is selective to the Si substrate and can be used as high-k removal as well.
  • TaN is etched with pure BCl 3 plasma, then a notch (lateral attack) is observed in the TaN layer.
  • FIG. 4A shows the gate profile after etching in pure BCl 3 , an arrow indicates the lateral attack of TaN.
  • a B x N y comprising passivation layer will be deposited onto the vertical sidewalls of the stack during patterning, said B x N y comprising passivation layer will protect the TaN during patterning and avoid lateral attack.
  • a straight TaN profile can also be obtained by using a BCl 3 /O 2 plasma mixture, as shown in FIG. 5B .
  • the presence of O 2 in the etching plasma will have a detrimental effect on the high-k dielectric and, therefore, is preferably avoided.
  • the B x N y comprising passivation layer can be removed by a wet treatment e.g. a removal in water.
  • the BCl 3 /N 2 plasma was used to pattern pure Ge gates having a high-k dielectric underneath (in the presented case the high-k dielectric is HfO 2 ).
  • the high-k dielectric must be removed selectively to the underlying Si substrate.
  • the Ge gate profile just after patterning and before high-k removal as shown in FIG. 2 is straight.
  • HfO 2 removal is etching in BCl 3 plasma. If high-k is removed by such plasma, the Ge gate suffers from profile distortion while addition of 10% N 2 to the BCl 3 plasma preserves the profile even if the removal time is doubled as shown in FIG. 3 .
  • FIG. 3A shows the Ge gate profile after high-k removal by a pure BCl 3 plasma for 10 seconds and FIG. 3B shows the Ge gate profile after high-k removal by a BCl 3 /N 2 (10% N 2 ) plasma for 20 seconds. No lateral attack of the Ge profile is seen in FIG. 3B .
  • the plasma parameters used for the deposition of a BxNy passivation film during TaN metal gate patterning as presented in Example 1 using a plasma of a preferred embodiment are as follows: pressure 0.666 Pa (5 mT), plasma power 450 W, flow BCl 3 95 sccm (standard centimeter cube per minute), flow N 2 5 sccm, and substrate bias 55V.
  • the plasma parameters used for the deposition of a BxNy passivation film during high-k removal in a Ge gate stacks as presented in Example 2 are as follows: pressure 0.666 Pa (5 mT), plasma power 450 W, substrate bias 30V, BCl 3 90 sccm, N 2 10 sccm.
  • Said BxNy film was characterized by Fourier Transmission Infra-Red spectrometry (FTIR) and X-ray Photoelectron Spectroscopy (XPS). It was found that a plasma mixture of BCl 3 and N 2 resulted in the deposition of a BxNy film onto a (flat) wafer surface if no bias was applied to the substrate (to avoid ion bombardment).
  • Said BxNy film was deposited in an etch chamber (LAM Versys 2300) at 60° C. and 275° C. at a rate as high as 300 nm/min depending on the pressure, plasma power, gas flows and BCl 3 to N 2 ratio.
  • LAM Versys 2300 etch chamber
  • FIG. 1 The FTIR spectra of the BxNy films deposited at 60° C. and 275° C. (for comparison) are shown in FIG. 1 .
  • a strong peak at about 1400 cm ⁇ 1 is attributed to a hexagonal boron nitride (h-BN). This peak dominate the spectrum of the film deposited at 275° C. but the spectrum of the film deposited at 60° C. contains number of other peaks and, therefore, that film is not pure BN.
  • h-BN hexagonal boron nitride
  • the XPS analysis of the surface of the film deposited at 60° C. showed primarily boron (about 36%), nitrogen (about 20%) and oxygen (about 36%). Some carbon (about 7%) is attributed to the contamination from the atmosphere. The amount of chlorine did not exceed 1%. As the deposition plasma contains no O 2 , the significant amount of oxygen in the film is a sign of the film oxidation during the atmosphere exposure.
  • the deposited BxNy-like film was found to be easily decomposing by temperature (the film thickness decreases at temperatures above 100° C.) and soluble in water at room temperatures. These properties make cleaning of any deposited inhibitor layer easy: the water rinse is enough to clean any BxNy-like film that is left after the gate patterning.

Abstract

A plasma composition and its use in a method for the dry etching of a stack of at least one material chemically too reactive towards the use of a Cl-based plasma are provided. Small amounts of nitrogen (5% up to 10%) can be added to a BCl3 comprising plasma and used in an anisotropical dry etching method whereby a passivation film is deposited onto the vertical sidewalls of stack etched for protecting the vertical sidewalls from lateral attack such that straight profiles can be obtained.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • This application claims the benefit under 35 U.S.C. § 119(e) of U.S. provisional application Ser. No. 60/731,608, filed Oct. 28, 2005, and U.S. provisional application Ser. No. 60/839,897, filed Aug. 23, 2006, the disclosures of which are hereby expressly incorporated by reference in their entirety and are hereby expressly made a portion of this application.
  • FIELD OF THE INVENTION
  • A method of dry etching of advanced gate stacks is provided which can be used to etch metal gate comprising stacks and pure germanium comprising stacks. An etch plasma composition is also provided for dry etching of metal gate comprising stacks and pure germanium comprising stacks, thereby preserving the vertical profile of the gate stack after patterning.
  • BACKGROUND OF THE INVENTION
  • As the critical dimensions in CMOS manufacturing shrink for the 90 nm technology node and beyond, conventional (poly) silicon gates are being replaced by metal gates (meaning pure metals, metal alloys or metal nitrides, etc) and SiO2 as a gate dielectric is replaced by materials with higher dielectric constant (so called “high-k dielectrics). The key challenge is to adapt the conventional gate etch process flow to the metal gate stack. Etching this metal gate stack now requires a process that defines the metal gate profile without affecting the gate critical dimension (CD) and stops on thin gate oxide without pitting or punch through.
  • Etching of metal gates has been studied addressing metal gate and gate oxide surface roughness, CD control, etch selectivity, and low damage etching but none of them succeeded in preserving the vertical profile of the gate stack after patterning.
  • One of the promising chemistry for patterning of advanced gate stacks (metal gate etch or high-k removal) is BCl3. The main advantage of this plasma is that it can etch both metal gates and high-k dielectric with reasonable selectivity to the Si substrate. However, there are number of gate stack materials that are incompatible with BCl3 plasma as they are too reactive. As a result, BCl3 produces some undesirable lateral etch that compromises the gate profiles. Two particular examples are Ge gates and TaN metal gates. If a pure BCl3 plasma is applied during the patterning of the gate stacks containing Ge or TaN a profile distortion caused by lateral etch is observed.
  • SUMMARY OF THE INVENTION
  • A dry-etch plasma composition for preserving the vertical profile of a structure comprising a stack of layers during anisotropical dry-etch patterning is provided.
  • Said plasma composition is further characterized such that during the dry-etch patterning of said stack a water-soluble film, which is removable against the structure, is deposited onto the sidewalls of said stack such that lateral attack of said patterned stack is avoided.
  • Preferably, the plasma composition of preferred embodiments is characterized as a plasma comprising a boron-halogen compound and nitrogen and wherein the ratio of the boron-halogen compound to nitrogen is from 19:1 up to 9:1. More preferred, the plasma composition of the preferred embodiments is characterized as a plasma composition wherein said plasma comprises a boron-halogen compound, nitrogen and optionally an inert compound. Most preferred said boron-halogen compound is BCl3.
  • Preferably, the plasma composition of the preferred embodiments is characterized as a plasma comprising (or consisting of) a boron-halogen compound and 5 up to 10% nitrogen (of the total plasma composition).
  • More preferably, the plasma composition comprises (or consists of) a boron-halogen compound and less than 10% nitrogen (of the total plasma composition). More particularly, said boron-halogen compound is BCl3.
  • Most preferred, said plasma is (i.e. consists of) a BCl3 plasma further comprising (or to which is added) from 5% to 10% nitrogen (based on the total plasma composition).
  • In a preferred embodiment, the stack of layers to be patterned is a metal gate comprising stack.
  • More preferred, said metal gate comprising stack comprises at least one TaN layer or combinations of a TaN layer and a TiN layer (referred to as TaN/TiN metal gates) wherein said TaN layer is too sensitive to a (pure) BCl3 plasma. Or in other words the stack of layers to be patterned is a stack wherein at least one layer of said stack of layers is a TaN layer.
  • In another preferred embodiment, at least one layer of said stack of layers to be patterned is a germanium comprising layer.
  • Said germanium layer can be situated upon a layer to be patterned by the plasma composition. Said germanium layer can be a pure Ge layer.
  • Preferably, the plasma of the preferred embodiments (during patterning) has a substrate bias which is different from zero.
  • Preferably, the plasma of the preferred embodiments (during patterning) has a plasma power of from 100 W up to 1200 W. More preferred said plasma power is about 450 W.
  • Preferably, the plasma of the preferred embodiments (during patterning) has a pressure in the plasma chamber of minimum 0.666 Pa (5 mT) and maximum 10.665 Pa (80 mT). More preferred said pressure is 0.666 Pa (5 mT).
  • Preferably, the plasma of the preferred embodiments (during patterning) has a temperature below 100° C. and most preferred said plasma temperature during dry-etch patterning is about 60° C.
  • An anisotropical dry etching method is also provided using the plasma composition of the preferred embodiments as described above for patterning a stack of layers to create a vertical structure wherein lateral attack during patterning of said stack is avoided.
  • Preferably said method comprises the steps of first applying a dry-etch step using the plasma composition of the preferred embodiments wherein during the etching a protective and water-soluble film is deposited onto the vertical sidewalls of said structure such that the vertical profile of said structure is preserved and lateral attack is avoided. In a next step said water-soluble film is removed from said structure.
  • Said water-soluble film is preferably removed using a wet removal process using water.
  • Use is provided of a plasma comprising (or consisting of) BCl3, to which nitrogen is added to reach 5% to 10% of the total volume of the resulting plasma composition, for etching a (suitable) stack of layer (i.e. comprising at least one layer etchable by said BCl3 component) and simultaneously passivating (or protecting) the sidewalls of said stack of layers from lateral etch.
  • A method is also provided for etching (or patterning) a (suitable) stack of layers while/and simultaneously passivating (or protecting) the sidewalls of said stack of layers comprising the step of providing a plasma comprising (or consisting of) BCl3, to which nitrogen is added to reach 5% to 10% of the total volume of the resulting plasma composition.
  • Said use or said method is particularly useful for (patterning) a stack of layers wherein at least one layer is germanium, or at least one layer is TaN.
  • Said passivating (or protecting) effect results from the formation and deposition of a film (or layer) which contains boron and nitrogen (and further compounds such as oxygen) on the sidewalls of said stack of layers. Said film obtainable by a method of the preferred embodiments is also provided.
  • Said use or said method can be carried out in the framework of CMOS manufacture.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • All drawings are intended to illustrate some aspects and embodiments of the present invention. Not all alternatives and options are shown and therefore the invention is not limited to the content of the given drawings.
  • FIG. 1 shows FTIR (Fourier Transform Infrared Spectroscopy) spectra of films deposited from BCl3/N2 plasma mixture (70% BCl3) at 275° C. and 60° C.
  • FIG. 2 shows a Ge gate profile after the gate patterning and before the high-k removal.
  • FIG. 3 shows a Ge gate profile after high-k removal by pure BCl3 plasma for 10 seconds (FIG. 3A) and BCl3/N2 (10% N2) plasma for 20 seconds (FIG. 3B)
  • FIG. 4 shows a TaN gate profile after etching in pure BCl3 plasma (FIG. 4A), an arrow indicates the lateral attack of TaN. FIG. 4B shows a TaN gate profile after etching in BCl3/N2 (5% N2) plasma.
  • FIG. 5 shows a TaN gate profile after etching in BCl3/N2 plasma (FIG. 5A) and a TaN gate profile after etching in BCl3/O2 plasma (FIG. 5B).
  • FIG. 6 illustrates the deposition rate of a BxNy film using a BCl3/N2plasma (Pressure=1,333 Pa (10 mT)).
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
  • Exemplary embodiments are illustrated in referenced figures of the drawings. It is intended that the embodiments and figures herein are to be considered illustrative rather than restrictive.
  • In the context of the preferred embodiments, the term “critical dimension” (CD) as used herein is a broad term, and is to be given its ordinary and customary meaning to a person of ordinary skill in the art (and is not to be limited to a special or customized meaning), and refers without limitation to the smallest dimensions of geometrical features (e.g. width of gate electrode) which can be formed during semiconductor device manufacturing. In the context of the preferred embodiments the term “bias” as used herein is a broad term, and is to be given its ordinary and customary meaning to a person of ordinary skill in the art (and is not to be limited to a special or customized meaning), and refers without limitation to the voltage applied to the substrate during patterning in a dry etch chamber.
  • The term “selectivity” as used herein is a broad term, and is to be given its ordinary and customary meaning to a person of ordinary skill in the art (and is not to be limited to a special or customized meaning), and refers without limitation to the etch rate of a selected material towards another material. The material to be etched away should have a much higher etch rate than the other materials.
  • The term “ratio” as used herein is a broad term, and is to be given its ordinary and customary meaning to a person of ordinary skill in the art (and is not to be limited to a special or customized meaning), and refers without limitation to an expression of an amount of a first compound to a second compound, e.g. a ratio of 9:1 means e.g. 9 sccm (standard centimeter cube per minute) of the first compound and 1 sccm of the second compound.
  • Use of plasma composition according to the preferred embodiments surprisingly results in the deposition of a BxNy film during the etching of a structure wherein the deposition is performed in a plasma etch chamber (e.g., Versys 2300 etch chamber from LAM®) at low temperatures (e.g. 60° C.), which was never reported before (BN deposition is usually performed at temperatures of 390° C.-650° C.). The BxNy film is deposited at a rate as high as 10 nm/min to more than 100 nm/min depending on the pressure, plasma power, gas flows, and plasma composition (more specifically the BCl3 to N2 ratio). Said deposited BxNy-like film, in contrast to a pure BN film, was found to be easily decomposing by temperature (the film thickness decreases at temperatures above 100° C.) and soluble in water at room temperatures.
  • The preferred embodiments are further related to the patterning of a stack of layers, more specifically to the dry etching of a stack of layers.
  • Said patterning is making use of a plasma etch compound wherein at least one of the layers is too sensitive to said etch compound. By adding an extra component to the plasma it is possible to deposit a protective layer onto the stack of layers such that said stack is protected for e.g. sidewall damage. Said protective layer is deposited during the patterning (dry etching). Furthermore said protective layer is sacrificial and hence easy removable.
  • The “sacrificial” layer, also referred to as “protective” layer or “passivation” layer refers to the BxNy like film resulting from the addition of nitrogen in the boron-halogen plasma, also referred to as BxNy film or as to boron nitride like film, which is deposited during etching. Said BxNy film is used as a “protective” or “passivating” film during patterning/etching of a structure, said BxNy film is also referred to as a sacrificial layer because said layer is removed after patterning is completed. Due the unstable character of the BxNy film and water soluble character said BxNy film can be easily removed by e.g. a water rinse.
  • The term “BxNy” film refers to a film comprising mainly boron and nitrogen which is further characterized as a water-soluble film. The BxNy film of the preferred embodiments is water soluble, in contrast to a pure BN which is insoluble in water. The BxNy film contains hexagonal boron nitride, but is very unlikely to be a stoichiometric BN. The BxNy film is therefore referred to as BxNy wherein the integers x and y indicate that the ratio of nitrogen and boron in the film is not fixed due to the presence of other compounds (impurities) in the film such as water, oxygen and/or ammonia which are possibly absorbed from the plasma and/or atmosphere after dry-etching.
  • More specifically, the preferred embodiments relate to the patterning of metal gate stacks or germanium gate stacks, more specifically it relates to the dry etching of said gate stacks such as TaN comprising metal gate stacks and to the dry etching of Ge comprising stacks (or in other words a stack comprising e.g. a pure Ge layer).
  • The methods and compositions of preferred embodiments can solve or minimize the problem of lateral etch and profile attack during the patterning of advanced gate stacks such as metal gate stacks and germanium stacks by adding small amounts of nitrogen to a boron-halogen plasma such as BCl3 plasma in order to improve gate profile control. The mixture of BCl3/N2 plasma results in a deposition of BxNy-like film that inhibits the lateral etch but does not inhibit vertical etch as the formed BxNy-like film is destroyed by ion bombardment.
  • A plasma composition is provided for patterning metal gate stacks and/or germanium stacks wherein during the patterning of said stack a protective and water-soluble film is deposited such that the vertical profile of the stack is preserved and lateral attack of said stack is avoided.
  • More specifically a plasma composition is provided for patterning a stack of layers wherein at least one layer of said stack is sensitive to one of the etch compounds.
  • The plasma composition is preferably a Boron-halogen comprising plasma with small additions of nitrogen.
  • The Boron-halogen compound is preferably BCl3 and said small additions of nitrogen are such that the ratio of the boron-halogen compound to nitrogen is from 19:1 up to 9:1.
  • Optionally an inert compound can be added to the plasma comprising boron-halogen and nitrogen. Said inert compound can be e.g. argon or helium (He) and these compounds can be added to the plasma in concentrations up to 50% of the total plasma composition. It is further known that addition of inert compounds (meaning that these compounds do not react with the substrate to be etched such that volatile compounds are formed) can improve the dissociation rate in the plasma and hence improve the etch rate and more specifically in case of the invention improve the formation (deposition) of a BxNy film. In that case the inert compound can be seen as a catalyst.
  • For the patterning of metal gates comprising TaN, such as TaN metal gates and metal gates comprising layers of TaN and TiN (TaN/TiN metal gates) the ratio of the boron-halogen compound to nitrogen is below 9:1 (having more boron-halogen), more preferred said ratio of the boron-halogen compound to nitrogen is below 11:1 and most preferred said ratio of the boron-halogen compound to nitrogen is 19:1.
  • For the patterning of metal gates comprising TaN, such as TaN metal gates and metal gates comprising combinations of TaN and TiN layers (TaN/TiN metal gates) the ratio of BCl3 to nitrogen is below 9:1, more preferred said ratio of BCl3 to nitrogen is below 11:1 and most preferred said ratio of BCl3 to nitrogen is 19:1.
  • For the patterning of germanium comprising stacks wherein germanium is at least one of the layers of the stack and said germanium layer needs to be protected to avoid lateral attack during patterning of a layer situated under said germanium layer, the ratio of the boron-halogen compound to nitrogen is higher than 19:1. More preferred said ratio of the boron-halogen compound to nitrogen is higher than 11:1 and most preferred the ratio of the boron-halogen compound to nitrogen is 9:1.
  • For the patterning of germanium comprising stacks wherein germanium is at least one of the layers of the stack said germanium layer needs to be protected to avoid lateral attack during patterning of a layer situated under said germanium layer, the ratio of BCl3 to nitrogen is higher than 19:1. More preferred said ratio of BCl3 to nitrogen is higher than 11:1 and most preferred the ratio of BCl3 to nitrogen is 9:1.
  • In a preferred embodiment, the plasma composition is preferably a plasma comprising (or consisting of) a Boron-halogen compound and nitrogen, or in other words small additions of nitrogen in a boron-halogen plasma.
  • Preferably, the plasma comprises (or consists of) a boron-halogen compound and 5% up to 10% nitrogen (of the total plasma composition).
  • More preferred, the plasma composition comprises (or consists of) a boron-halogen compound and less than 10% nitrogen (of the total plasma composition) and most preferred said boron-halogen is BCl3.
  • For the patterning of germanium comprising stacks wherein said germanium layer needs to be protected to avoid lateral attack during patterning of a layer situated under said germanium layer, the amount of N2 to the total BCl3/N2 plasma composition is higher than 5%, more preferred said amount of N2 is higher than 8% N2 to the total BCl3/N2 plasma composition and most preferred said amount of N2 is 10% to the total BCl3/N2 plasma composition.
  • For the patterning of metal gates such as TaN and/or combinations of TaN and TiN (TaN/TiN metal gates) the amount of N2 to the total BCl3/N2 plasma composition is lower than 10%, more preferred said amount of N2 is lower than 8% N2 to the total BCl3/N2 plasma composition and most preferred said amount of N2 is 5% to the total BCl3/N2 plasma composition.
  • Preferably the plasma of the preferred embodiments (during patterning) has a substrate bias which is different from zero.
  • Preferably the plasma of the preferred embodiments (during patterning) has a plasma power is from 100 W up to 1200 W. More preferred said plasma power is about 450 W.
  • Preferably the plasma of the preferred embodiments (during patterning) has a pressure in the plasma chamber of minimum 0.666 Pa (5 mT) and maximum 10.665 Pa (80 mT). More preferred said pressure is 0.666 Pa (5 mT).
  • Preferably the plasma of the preferred embodiments (during patterning) has a temperature below 100° C. and most preferred said plasma temperature during dry-etch patterning is about 60° C. A boron-nitrogen (BxNy or BN) film deposited at higher temperatures is equal to a higher quality film containing less (or no) impurities which is more difficult or even not possible to remove.
  • A method is provided for the dry etching of non-Si comprising gate stacks, said non-Si comprising gate stacks are preferably metal gate comprising gate stacks such as TaN comprising gate stacks and preferably metal gate stacks comprising a (pure) germanium layer.
  • More specifically the dry-etching method of the preferred embodiments uses a plasma composition wherein at least one layer of said stack is too sensitive to one of the etch compounds.
  • Said dry etching method is characterized in that the vertical profile of said gate stack is preserved after etching. The method of the preferred embodiments solves or minimizes the problem of negatively sloped gate profiles after dry etching by depositing a sacrificial layer during the etching. Said sacrificial layer serves as a passivating layer during dry etching such that the vertical profile or CD of the gate stack is preserved.
  • The dry-etching method of the preferred embodiments solves or minimizes the problem of lateral etch and profile attack during the patterning of advanced gate stacks such as metal gate stacks and germanium comprising stacks by adding small amounts of nitrogen to a boron-halogen plasma such as BCl3 plasma in order to improve gate profile control. The mixture of BCl3/N2 plasma results in a deposition of BxNy-like film that inhibits the lateral etch but does not inhibit vertical etch as the formed BxNy-like film is destroyed by ion bombardment.
  • Preferably the method of the preferred embodiments comprises the steps of first applying a dry-etch step using the plasma composition of the preferred embodiments whereby during the etching a protective and water-soluble film is deposited onto the vertical sidewalls of said structure such that the vertical profile of said structure is preserved and lateral attack is avoided. In a next step said water-soluble film is removed from said structure.
  • Said water-soluble film is preferably removed using a wet removal process, most preferred said wet removal is using water.
  • The dry-etching method of the preferred embodiments uses a boron-halogen comprising plasma with small additions of nitrogen.
  • The Boron-halogen compound is preferably BCl3 and said small additions of nitrogen are such that the ratio of the boron-halogen compound to nitrogen is from 19:1 up to 9:1.
  • Optionally an inert compound can be added to the plasma comprising boron-halogen and nitrogen. Said inert compound can be e.g. argon or helium (He) and these compounds can be added to the plasma in concentrations up to 50% of the total plasma composition.
  • In a method of the preferred embodiments for patterning metal gates such as TaN metal gates and metal gates comprising combinations of TaN and TiN (TaN/TiN metal gates), the ratio of the boron-halogen compound to nitrogen is preferably below 9:1. More preferably, said ratio of the boron-halogen compound to nitrogen is below 11:1 and most preferred said ratio of the boron-halogen compound to nitrogen is 19:1.
  • In particular, said boron-halogen compound is BCl3.
  • In a method of the preferred embodiments for patterning germanium comprising stacks, wherein said germanium layer is a layer of the stack which needs to be protected to avoid lateral attack during patterning of a layer situated under said germanium layer, the ratio of the boron-halogen compound to nitrogen is preferably higher than 19:1. More preferred said ratio of the boron-halogen compound to nitrogen is higher than 11:1 and most preferred the ratio of the boron-halogen compound to nitrogen is 9:1.
  • In particular, said boron-halogen compound is BCl3.
  • In a preferred embodiment, the plasma composition used in a method of the preferred embodiments is a plasma comprising (or consisting of) a Boron-halogen compound and nitrogen, or in other words small additions of nitrogen in a boron-halogen plasma.
  • Preferably, the plasma comprises (or consists of) a boron-halogen compound and 5% up to 10% nitrogen (of the total plasma composition).
  • More preferred, the plasma composition comprises (or consists of) a boron-halogen compound and less than 10% nitrogen (of the total plasma composition) and most preferred said boron-halogen is BCl3.
  • In a method of the preferred embodiments for patterning germanium comprising stacks wherein said germanium layer needs to be protected to avoid lateral attack during patterning of a layer situated under said germanium layer, the amount of N2 to the total BCl3/N2 plasma composition is higher than 5%, more preferred said amount of N2 is higher than 8% N2 to the total BCl3/N2 plasma composition and most preferred said amount of N2 is 10% to the total BCl3/N2 plasma composition.
  • In a method of the preferred embodiments for patterning metal gates such as TaN and/or combinations of TaN and TiN (TaN/TiN metal gates), the amount of N2 to the total BCl3/N2 plasma composition is lower than 10%, more preferred said amount of N2 is lower than 8% N2 to the total BCl3/N2 plasma composition and most preferred said amount of N2 is 5% to the total BCl3/N2 plasma composition.
  • Preferably the plasma used in a method of the preferred embodiments (during patterning) has a substrate bias which is different from zero.
  • Preferably, said plasma has a plasma power of 100 W up to 1200 W. More preferred said plasma power is about 450 W.
  • Preferably, said plasma has a pressure in the plasma chamber of minimum 0.666 Pa (5 mT) and maximum 10.665 Pa (80 mT). More preferred said pressure is 0.666 Pa (5 mT).
  • Preferably, said plasma has a temperature below 100° C. and more preferred said plasma temperature during dry-etch patterning is about 60° C.
  • Indeed, a boron-nitrogen (BxNy or BN) film deposited at higher temperatures is equal to a higher quality film containing less (or no) impurities, which is more difficult or even not possible to remove.
  • In relation to the drawings the preferred embodiments can also be described as follows in the text below.
  • A method is provided for the dry etching of non-Si comprising gate stacks, said non-Si comprising gate stacks are preferably metal gate comprising gate stacks such as TaN comprising gate stacks and preferably pure germanium comprising metal stacks. Said dry etching method is characterized in that the vertical profile of said gate stack is preserved after etching. The method of the preferred embodiments solves the problem of negatively sloped gate profiles after dry etching by depositing a sacrificial layer during the etching. Said sacrificial layer serves as a passivating layer during dry etching such that the vertical profile or CD of the gate stack is preserved.
  • A composition is provided of a plasma used to etch materials that are too sensitive to Cl-based plasmas. If those materials are etched with pure Cl-based plasmas such as BCl3 plasmas, the etch profiles are distorted because these materials are etched in the lateral direction as well. Examples of said materials are metal gate comprising gate stacks such as TaN comprising gate stacks and pure germanium comprising metal stacks. The plasma of the preferred embodiments solves or minimizes the problem of damage caused by Cl-based plasmas, more specifically this is achieved by adding small amounts of nitrogen to the Cl-based plasma. For the patterning of metal gate comprising gate stacks such as TaN comprising gate stacks and pure germanium comprising metal stacks said Cl compound is preferably BCl3. The amount of nitrogen added to the plasma is preferably from 5% up to 10%. The addition of nitrogen to a Cl-based plasma such as BCl3 preserves the vertical profile through the formation of a passivating BxNy-like layer on the vertical surfaces.
  • A Cl-based plasma with small additions of nitrogen for the patterning of non-Si based stacks is also provided. Said patterning is further characterized as a patterning which avoids lateral etching and preserves the vertical profile. Said stacks are preferably metal gate comprising gate stacks such as TaN comprising gate stacks and preferably pure germanium comprising metal stacks. For patterning TaN comprising gate stacks and pure Germanium comprising gate stacks, said Cl compound is BCl3.
  • EXAMPLES
  • The method of the preferred embodiments as well as the plasma and its use can be applied to any material that can be etched by Cl-based plasma but is too chemically reactive and has significant lateral etch component. Said lateral etch can be blocked by a BxNy-like passivation film deposited onto the vertical sidewalls while at the meanwhile the vertical etch is not significantly affected.
  • The BCl3/N2 plasma was applied for patterning of two different stacks as described in Example 1 and 2: pure Ge gates and TaN metal gates in the TiN/TaN gate stack. In both cases, the lateral attack of the gate material was prevented by addition of small amount of N2 (5%-10%) to the BCl3 plasma. Furthermore the plasma settings were optimized and illustrated in Example 3. The deposited (passivation) BxNy-like layer of the preferred embodiments is characterized by FTIR and illustrated in Example 4.
  • Example 1 Application of BCl3/N2 Plasma for TaN Gate Profile Control
  • The BCl3/N2 plasma was used to etch TaN metal gates, in the example presented here said TaN metal gate is present in a TiN/TaN gate stack where 15 nm TaN is in the contact with the gate dielectric and 70 nm TiN covers the TaN or in other words 70 nm TiN is situated on top of said 15 nm TaN.
  • The most critical step is TaN etching after TiN patterning. BCl3 plasma is used here for the TaN patterning as it is selective to the Si substrate and can be used as high-k removal as well.
  • If TaN is etched with pure BCl3 plasma, then a notch (lateral attack) is observed in the TaN layer.
  • FIG. 4A shows the gate profile after etching in pure BCl3, an arrow indicates the lateral attack of TaN.
  • The addition of 5% of N2 to the BCl3 plasma resulted in a straight TaN profile without the lateral attack of the TaN layer.
  • The effect of N2 addition is illustrated in FIG. 4B. A BxNy comprising passivation layer will be deposited onto the vertical sidewalls of the stack during patterning, said BxNy comprising passivation layer will protect the TaN during patterning and avoid lateral attack.
  • The deposition of a BxNy comprising layer onto the horizontal surfaces will be negligible due to a continuous ion bombardment in the vertical direction (in other words the BxNy comprising layer will be removed immediately after deposition onto horizontal surfaces).
  • This means that the deposition of the BxNy like film inhibits the lateral etch but does not inhibit vertical etch as the formed BxNy-like film is destroyed by ion bombardment.
  • A straight TaN profile can also be obtained by using a BCl3/O2 plasma mixture, as shown in FIG. 5B. However, the presence of O2 in the etching plasma will have a detrimental effect on the high-k dielectric and, therefore, is preferably avoided.
  • After patterning of the TaN comprising gate stack, the BxNy comprising passivation layer can be removed by a wet treatment e.g. a removal in water.
  • Example 2 Application of BCl3/N2 Plasma for Pure Ge Gate Profile Control
  • The BCl3/N2 plasma was used to pattern pure Ge gates having a high-k dielectric underneath (in the presented case the high-k dielectric is HfO2). The high-k dielectric must be removed selectively to the underlying Si substrate.
  • The Ge gate profile just after patterning and before high-k removal as shown in FIG. 2 is straight.
  • The conventional way of HfO2 removal is etching in BCl3 plasma. If high-k is removed by such plasma, the Ge gate suffers from profile distortion while addition of 10% N2 to the BCl3 plasma preserves the profile even if the removal time is doubled as shown in FIG. 3.
  • FIG. 3A shows the Ge gate profile after high-k removal by a pure BCl3 plasma for 10 seconds and FIG. 3B shows the Ge gate profile after high-k removal by a BCl3/N2 (10% N2) plasma for 20 seconds. No lateral attack of the Ge profile is seen in FIG. 3B.
  • It can be concluded that addition of small amounts of N2 (in the presented case 10% N2 was added) to the BCl3 plasma during high-k removal preserves the shape of the Ge gate. This is due to the deposition of a BxNy-like passivation film on the gate (vertical) sidewalls. Said BxNy-like passivation film is a sacrificial layer which can be removed afterwards by wet treatment.
  • Example 3 Plasma Parameters Used to Deposit a BxNy Passivation Film
  • The plasma parameters used for the deposition of a BxNy passivation film during TaN metal gate patterning as presented in Example 1 using a plasma of a preferred embodiment are as follows: pressure 0.666 Pa (5 mT), plasma power 450 W, flow BCl3 95 sccm (standard centimeter cube per minute), flow N 2 5 sccm, and substrate bias 55V.
  • The plasma parameters used for the deposition of a BxNy passivation film during high-k removal in a Ge gate stacks as presented in Example 2 are as follows: pressure 0.666 Pa (5 mT), plasma power 450 W, substrate bias 30V, BCl3 90 sccm, N2 10 sccm.
  • Example 4 Characterization of the Deposited BxNy Layer
  • Using the plasma composition (BCl3/N2) and method of the preferred embodiments resulted in the deposition of a BxNy layer. Said BxNy film was characterized by Fourier Transmission Infra-Red spectrometry (FTIR) and X-ray Photoelectron Spectroscopy (XPS). It was found that a plasma mixture of BCl3 and N2 resulted in the deposition of a BxNy film onto a (flat) wafer surface if no bias was applied to the substrate (to avoid ion bombardment). Said BxNy film was deposited in an etch chamber (LAM Versys 2300) at 60° C. and 275° C. at a rate as high as 300 nm/min depending on the pressure, plasma power, gas flows and BCl3 to N2 ratio.
  • The FTIR spectra of the BxNy films deposited at 60° C. and 275° C. (for comparison) are shown in FIG. 1. A strong peak at about 1400 cm−1 is attributed to a hexagonal boron nitride (h-BN). This peak dominate the spectrum of the film deposited at 275° C. but the spectrum of the film deposited at 60° C. contains number of other peaks and, therefore, that film is not pure BN.
  • The XPS analysis of the surface of the film deposited at 60° C. showed primarily boron (about 36%), nitrogen (about 20%) and oxygen (about 36%). Some carbon (about 7%) is attributed to the contamination from the atmosphere. The amount of chlorine did not exceed 1%. As the deposition plasma contains no O2, the significant amount of oxygen in the film is a sign of the film oxidation during the atmosphere exposure.
  • The deposited BxNy-like film was found to be easily decomposing by temperature (the film thickness decreases at temperatures above 100° C.) and soluble in water at room temperatures. These properties make cleaning of any deposited inhibitor layer easy: the water rinse is enough to clean any BxNy-like film that is left after the gate patterning.
  • It can be concluded that by mixing BCl3 and N2 in a plasma etch chamber it is possible to deposit a BxNy-like film that contains almost no Cl2. The film is relatively unstable and can be easily removed by a water rinse, as it is soluble in water.
  • All references cited herein are incorporated herein by reference in their entirety. To the extent publications and patents or patent applications incorporated by reference contradict the disclosure contained in the specification, the specification is intended to supersede and/or take precedence over any such contradictory material.
  • The term “comprising” as used herein is synonymous with “including,” “containing,” or “characterized by,” and is inclusive or open-ended and does not exclude additional, unrecited elements or method steps.
  • All numbers expressing quantities of ingredients, reaction conditions, and so forth used in the specification and claims are to be understood as being modified in all instances by the term “about.” Accordingly, unless indicated to the contrary, the numerical parameters set forth in the specification and attached claims are approximations that may vary depending upon the desired properties sought to be obtained by the present invention. At the very least, and not as an attempt to limit the application of the doctrine of equivalents to the scope of the claims, each numerical parameter should be construed in light of the number of significant digits and ordinary rounding approaches.
  • The above description provides several methods and materials of the present invention. This invention is susceptible to modifications in the methods and materials, as well as alterations in the fabrication methods and equipment. Such modifications will become apparent to those skilled in the art from a consideration of this disclosure or practice of the invention disclosed herein. Consequently, it is not intended that this invention be limited to the specific embodiments disclosed herein, but that it cover all modifications and alternatives coming within the true scope and spirit of the invention as embodied in the attached claims.

Claims (40)

1. A dry-etch plasma composition for preserving a vertical profile of a structure comprising a stack of layers, wherein a removable water-soluble film is deposited onto the sidewalls of the stack from the plasma composition during dry-etch patterning of the stack, such that lateral attack of the patterned stack is avoided.
2. The plasma composition of claim 1, wherein the plasma comprises a boron-halogen compound and nitrogen.
3. The plasma composition of claim 2, further comprising an inert compound.
4. The plasma composition of claim 2, wherein a ratio of the boron-halogen compound to nitrogen is from 19:1 to 9:1.
5. The plasma composition of claim 2, wherein the boron-halogen compound is BCl3.
6. The plasma composition of claim 1, wherein the stack of layers is a metal gate-comprising stack.
7. The plasma composition of claim 6, wherein the metal gate-comprising stack comprises TaN or TaN/TiN.
8. The plasma composition of claim 6, wherein at least one layer of the stack of layers is a germanium-comprising layer.
9. The plasma composition of claim 8, wherein the germanium layer is situated upon a layer to be patterned by the plasma composition.
10. The plasma composition of claim 1, wherein the substrate bias is different from zero.
11. The plasma composition of claim 1, wherein the plasma power is from 100 W to 1200 W.
12. The plasma composition of claim 11, wherein the plasma power is about 450 W.
13. The plasma composition of claim 1, wherein the pressure in the plasma chamber is from 0.666 Pa to 10.665 Pa.
14. The plasma composition of claim 1, wherein the pressure in the plasma chamber is 0.666 Pa.
15. The plasma composition of claim 1, wherein a temperature of the plasma during patterning is below 100° C.
16. The plasma composition of claim 1, wherein a temperature of the plasma during patterning is about 60° C.
17. The plasma composition of claim 1, wherein the plasma consists of a boron-halogen compound and nitrogen, and wherein from 5% to 10% of the total plasma composition is nitrogen.
18. The plasma composition of claim 1, wherein the plasma consists of a boron-halogen compound and nitrogen, and wherein less than 10% of the total plasma composition is nitrogen.
19. The plasma composition of claim 1, wherein the plasma consists of a boron-halogen compound and nitrogen, and wherein less than 8% of the total plasma composition is nitrogen.
20. The plasma composition of claim 1, wherein the plasma is a BCl3 plasma wherein 5% of the total plasma composition is nitrogen.
21. An anisotropical dry etching method for patterning a stack of layers to create a vertical structure, the method comprising the steps of:
patterning a stack of layers to create a vertical structure by dry etching using a plasma composition comprising a boron-halogen compound and nitrogen, wherein a protective and water-soluble film is deposited from the plasma onto vertical sidewalls of the structure during dry etching, such that a vertical profile of the structure is preserved and lateral attack is avoided during dry etching; and
removing the film from the structure.
22. The method of claim 21, wherein the film is removed by a wet removal process using water.
23. The method of claim 21, wherein a ratio of boron-halogen compound to nitrogen is from 19:1 to 9:1.
24. The method of claim 21, wherein the boron-halogen compound is BCl3.
25. The method of claim 21, wherein the plasma further comprises an inert compound.
26. The method of claim 21, wherein the stack of layers is a metal gate-comprising stack.
27. The method of claim 26, wherein the metal gate-comprising stack comprises TaN or TaN/TiN.
28. The method of claim 26, wherein at least one layer of the stack of layers comprises germanium.
29. The method of claim 28 wherein the germanium-comprising layer is situated upon a layer to be patterned by the plasma composition.
30. The method of claim 21, wherein a substrate bias during patterning is different from zero.
31. The method of claim 21, wherein a plasma power during patterning is from 100 W to 1200 W.
32. The method of claim 21, wherein a plasma power during patterning is about 450 W.
33. The method of claim 21, wherein a pressure in the plasma chamber during patterning is from 0.666 Pa to 10.665 Pa.
34. The method of claim 21, wherein a pressure in the plasma chamber during patterning is 0.666 Pa.
35. The method of claim 21, wherein the temperature of the plasma during patterning is below 100° C.
36. The method of claim 21, wherein the temperature of the plasma during patterning is about 60° C.
37. The method of claim 21, wherein the plasma consists of a boron-halogen compound and nitrogen, and wherein from 5% to 10% of the total plasma composition is nitrogen.
38. The method of claim 21, wherein the plasma consists of a boron-halogen compound and nitrogen, and wherein less than 10% of the total plasma composition is nitrogen.
39. The method of a claim 21, wherein the plasma consists of a boron-halogen compound and nitrogen, and wherein less than 8% of the total plasma composition is nitrogen.
40. The method of claim 21, wherein the plasma is a BCl3 plasma wherein 5% of the total plasma composition is nitrogen.
US11/544,351 2005-10-28 2006-10-05 Plasma for patterning advanced gate stacks Abandoned US20070099428A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US11/544,351 US20070099428A1 (en) 2005-10-28 2006-10-05 Plasma for patterning advanced gate stacks

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US73160805P 2005-10-28 2005-10-28
US83989706P 2006-08-23 2006-08-23
EP06121143A EP1780779A3 (en) 2005-10-28 2006-09-22 A plasma for patterning advanced gate stacks
EP06121143.9 2006-09-22
US11/544,351 US20070099428A1 (en) 2005-10-28 2006-10-05 Plasma for patterning advanced gate stacks

Publications (1)

Publication Number Publication Date
US20070099428A1 true US20070099428A1 (en) 2007-05-03

Family

ID=37776895

Family Applications (2)

Application Number Title Priority Date Filing Date
US11/544,351 Abandoned US20070099428A1 (en) 2005-10-28 2006-10-05 Plasma for patterning advanced gate stacks
US11/585,564 Active 2028-01-25 US7598184B2 (en) 2005-10-28 2006-10-24 Plasma composition for selective high-k etch

Family Applications After (1)

Application Number Title Priority Date Filing Date
US11/585,564 Active 2028-01-25 US7598184B2 (en) 2005-10-28 2006-10-24 Plasma composition for selective high-k etch

Country Status (3)

Country Link
US (2) US20070099428A1 (en)
EP (2) EP1780779A3 (en)
JP (1) JP5328094B2 (en)

Cited By (145)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110092040A1 (en) * 2009-10-19 2011-04-21 Samsung Electronics Co., Ltd. Semiconductor device and method for fabricating the same
US8895449B1 (en) 2013-05-16 2014-11-25 Applied Materials, Inc. Delicate dry clean
US8927390B2 (en) 2011-09-26 2015-01-06 Applied Materials, Inc. Intrench profile
US8951429B1 (en) 2013-10-29 2015-02-10 Applied Materials, Inc. Tungsten oxide processing
US8956980B1 (en) 2013-09-16 2015-02-17 Applied Materials, Inc. Selective etch of silicon nitride
US9023732B2 (en) 2013-03-15 2015-05-05 Applied Materials, Inc. Processing systems and methods for halide scavenging
US9040422B2 (en) * 2013-03-05 2015-05-26 Applied Materials, Inc. Selective titanium nitride removal
US9093390B2 (en) 2013-03-07 2015-07-28 Applied Materials, Inc. Conformal oxide dry etch
US9117855B2 (en) 2013-12-04 2015-08-25 Applied Materials, Inc. Polarity control for remote plasma
US9114438B2 (en) 2013-05-21 2015-08-25 Applied Materials, Inc. Copper residue chamber clean
US9132436B2 (en) 2012-09-21 2015-09-15 Applied Materials, Inc. Chemical control features in wafer process equipment
US9136273B1 (en) 2014-03-21 2015-09-15 Applied Materials, Inc. Flash gate air gap
US9159606B1 (en) 2014-07-31 2015-10-13 Applied Materials, Inc. Metal air gap
US9165786B1 (en) 2014-08-05 2015-10-20 Applied Materials, Inc. Integrated oxide and nitride recess for better channel contact in 3D architectures
US9190293B2 (en) 2013-12-18 2015-11-17 Applied Materials, Inc. Even tungsten etch for high aspect ratio trenches
US9236266B2 (en) 2011-08-01 2016-01-12 Applied Materials, Inc. Dry-etch for silicon-and-carbon-containing films
US9236265B2 (en) 2013-11-04 2016-01-12 Applied Materials, Inc. Silicon germanium processing
US9245762B2 (en) 2013-12-02 2016-01-26 Applied Materials, Inc. Procedure for etch rate consistency
US9263278B2 (en) 2013-12-17 2016-02-16 Applied Materials, Inc. Dopant etch selectivity control
US9269590B2 (en) 2014-04-07 2016-02-23 Applied Materials, Inc. Spacer formation
US9287095B2 (en) 2013-12-17 2016-03-15 Applied Materials, Inc. Semiconductor system assemblies and methods of operation
US9287134B2 (en) 2014-01-17 2016-03-15 Applied Materials, Inc. Titanium oxide etch
US9293568B2 (en) 2014-01-27 2016-03-22 Applied Materials, Inc. Method of fin patterning
US9299537B2 (en) 2014-03-20 2016-03-29 Applied Materials, Inc. Radial waveguide systems and methods for post-match control of microwaves
US9299583B1 (en) 2014-12-05 2016-03-29 Applied Materials, Inc. Aluminum oxide selective etch
US9299575B2 (en) 2014-03-17 2016-03-29 Applied Materials, Inc. Gas-phase tungsten etch
US9299538B2 (en) 2014-03-20 2016-03-29 Applied Materials, Inc. Radial waveguide systems and methods for post-match control of microwaves
US9309598B2 (en) 2014-05-28 2016-04-12 Applied Materials, Inc. Oxide and metal removal
US9324576B2 (en) 2010-05-27 2016-04-26 Applied Materials, Inc. Selective etch for silicon films
US9343272B1 (en) 2015-01-08 2016-05-17 Applied Materials, Inc. Self-aligned process
US9349605B1 (en) 2015-08-07 2016-05-24 Applied Materials, Inc. Oxide etch selectivity systems and methods
US9355856B2 (en) 2014-09-12 2016-05-31 Applied Materials, Inc. V trench dry etch
US9355862B2 (en) 2014-09-24 2016-05-31 Applied Materials, Inc. Fluorine-based hardmask removal
US9355863B2 (en) 2012-12-18 2016-05-31 Applied Materials, Inc. Non-local plasma oxide etch
US9362130B2 (en) 2013-03-01 2016-06-07 Applied Materials, Inc. Enhanced etching processes using remote plasma sources
US9368364B2 (en) 2014-09-24 2016-06-14 Applied Materials, Inc. Silicon etch process with tunable selectivity to SiO2 and other materials
US9373522B1 (en) 2015-01-22 2016-06-21 Applied Mateials, Inc. Titanium nitride removal
US9373517B2 (en) 2012-08-02 2016-06-21 Applied Materials, Inc. Semiconductor processing with DC assisted RF power for improved control
US9378978B2 (en) 2014-07-31 2016-06-28 Applied Materials, Inc. Integrated oxide recess and floating gate fin trimming
US9378969B2 (en) 2014-06-19 2016-06-28 Applied Materials, Inc. Low temperature gas-phase carbon removal
US9384997B2 (en) 2012-11-20 2016-07-05 Applied Materials, Inc. Dry-etch selectivity
US9385028B2 (en) 2014-02-03 2016-07-05 Applied Materials, Inc. Air gap process
US9390937B2 (en) 2012-09-20 2016-07-12 Applied Materials, Inc. Silicon-carbon-nitride selective etch
US9396989B2 (en) 2014-01-27 2016-07-19 Applied Materials, Inc. Air gaps between copper lines
US9406523B2 (en) 2014-06-19 2016-08-02 Applied Materials, Inc. Highly selective doped oxide removal method
US9412608B2 (en) 2012-11-30 2016-08-09 Applied Materials, Inc. Dry-etch for selective tungsten removal
US9418858B2 (en) 2011-10-07 2016-08-16 Applied Materials, Inc. Selective etch of silicon by way of metastable hydrogen termination
US9425058B2 (en) 2014-07-24 2016-08-23 Applied Materials, Inc. Simplified litho-etch-litho-etch process
US9437451B2 (en) 2012-09-18 2016-09-06 Applied Materials, Inc. Radical-component oxide etch
US9449845B2 (en) 2012-12-21 2016-09-20 Applied Materials, Inc. Selective titanium nitride etching
US9449846B2 (en) 2015-01-28 2016-09-20 Applied Materials, Inc. Vertical gate separation
US9472417B2 (en) 2013-11-12 2016-10-18 Applied Materials, Inc. Plasma-free metal etch
US9478432B2 (en) 2014-09-25 2016-10-25 Applied Materials, Inc. Silicon oxide selective removal
US9496167B2 (en) 2014-07-31 2016-11-15 Applied Materials, Inc. Integrated bit-line airgap formation and gate stack post clean
US9493879B2 (en) 2013-07-12 2016-11-15 Applied Materials, Inc. Selective sputtering for pattern transfer
US9502258B2 (en) 2014-12-23 2016-11-22 Applied Materials, Inc. Anisotropic gap etch
US9499898B2 (en) 2014-03-03 2016-11-22 Applied Materials, Inc. Layered thin film heater and method of fabrication
US9553102B2 (en) 2014-08-19 2017-01-24 Applied Materials, Inc. Tungsten separation
US9576809B2 (en) 2013-11-04 2017-02-21 Applied Materials, Inc. Etch suppression with germanium
US9659753B2 (en) 2014-08-07 2017-05-23 Applied Materials, Inc. Grooved insulator to reduce leakage current
US9691645B2 (en) 2015-08-06 2017-06-27 Applied Materials, Inc. Bolted wafer chuck thermal management systems and methods for wafer processing systems
US9721789B1 (en) 2016-10-04 2017-08-01 Applied Materials, Inc. Saving ion-damaged spacers
US9728437B2 (en) 2015-02-03 2017-08-08 Applied Materials, Inc. High temperature chuck for plasma processing systems
US9741593B2 (en) 2015-08-06 2017-08-22 Applied Materials, Inc. Thermal management systems and methods for wafer processing systems
US9768034B1 (en) 2016-11-11 2017-09-19 Applied Materials, Inc. Removal methods for high aspect ratio structures
US9773648B2 (en) 2013-08-30 2017-09-26 Applied Materials, Inc. Dual discharge modes operation for remote plasma
US9842744B2 (en) 2011-03-14 2017-12-12 Applied Materials, Inc. Methods for etch of SiN films
US9847289B2 (en) 2014-05-30 2017-12-19 Applied Materials, Inc. Protective via cap for improved interconnect performance
US9865484B1 (en) 2016-06-29 2018-01-09 Applied Materials, Inc. Selective etch using material modification and RF pulsing
US9881805B2 (en) 2015-03-02 2018-01-30 Applied Materials, Inc. Silicon selective removal
US9887096B2 (en) 2012-09-17 2018-02-06 Applied Materials, Inc. Differential silicon oxide etch
US9885117B2 (en) 2014-03-31 2018-02-06 Applied Materials, Inc. Conditioned semiconductor system parts
US9934942B1 (en) 2016-10-04 2018-04-03 Applied Materials, Inc. Chamber with flow-through source
US9947549B1 (en) 2016-10-10 2018-04-17 Applied Materials, Inc. Cobalt-containing material removal
US10026621B2 (en) 2016-11-14 2018-07-17 Applied Materials, Inc. SiN spacer profile patterning
US10043684B1 (en) 2017-02-06 2018-08-07 Applied Materials, Inc. Self-limiting atomic thermal etching systems and methods
US10043674B1 (en) 2017-08-04 2018-08-07 Applied Materials, Inc. Germanium etching systems and methods
US10049891B1 (en) 2017-05-31 2018-08-14 Applied Materials, Inc. Selective in situ cobalt residue removal
US10062587B2 (en) 2012-07-18 2018-08-28 Applied Materials, Inc. Pedestal with multi-zone temperature control and multiple purge capabilities
US10062579B2 (en) 2016-10-07 2018-08-28 Applied Materials, Inc. Selective SiN lateral recess
US10062578B2 (en) 2011-03-14 2018-08-28 Applied Materials, Inc. Methods for etch of metal and metal-oxide films
US10062585B2 (en) 2016-10-04 2018-08-28 Applied Materials, Inc. Oxygen compatible plasma source
US10062575B2 (en) 2016-09-09 2018-08-28 Applied Materials, Inc. Poly directional etch by oxidation
US10128086B1 (en) 2017-10-24 2018-11-13 Applied Materials, Inc. Silicon pretreatment for nitride removal
US10163696B2 (en) 2016-11-11 2018-12-25 Applied Materials, Inc. Selective cobalt removal for bottom up gapfill
US10170336B1 (en) 2017-08-04 2019-01-01 Applied Materials, Inc. Methods for anisotropic control of selective silicon removal
US10170282B2 (en) 2013-03-08 2019-01-01 Applied Materials, Inc. Insulated semiconductor faceplate designs
US10224210B2 (en) 2014-12-09 2019-03-05 Applied Materials, Inc. Plasma processing system with direct outlet toroidal plasma source
US10242908B2 (en) 2016-11-14 2019-03-26 Applied Materials, Inc. Airgap formation with damage-free copper
US10256112B1 (en) 2017-12-08 2019-04-09 Applied Materials, Inc. Selective tungsten removal
US10283321B2 (en) 2011-01-18 2019-05-07 Applied Materials, Inc. Semiconductor processing system and methods using capacitively coupled plasma
US10283324B1 (en) 2017-10-24 2019-05-07 Applied Materials, Inc. Oxygen treatment for nitride etching
US10297458B2 (en) 2017-08-07 2019-05-21 Applied Materials, Inc. Process window widening using coated parts in plasma etch processes
US10319739B2 (en) 2017-02-08 2019-06-11 Applied Materials, Inc. Accommodating imperfectly aligned memory holes
US10319649B2 (en) 2017-04-11 2019-06-11 Applied Materials, Inc. Optical emission spectroscopy (OES) for remote plasma monitoring
US10319600B1 (en) 2018-03-12 2019-06-11 Applied Materials, Inc. Thermal silicon etch
US10354889B2 (en) 2017-07-17 2019-07-16 Applied Materials, Inc. Non-halogen etching of silicon-containing materials
US10403507B2 (en) 2017-02-03 2019-09-03 Applied Materials, Inc. Shaped etch profile with oxidation
US10431429B2 (en) 2017-02-03 2019-10-01 Applied Materials, Inc. Systems and methods for radial and azimuthal control of plasma uniformity
US10468267B2 (en) 2017-05-31 2019-11-05 Applied Materials, Inc. Water-free etching methods
US10490406B2 (en) 2018-04-10 2019-11-26 Appled Materials, Inc. Systems and methods for material breakthrough
US10490418B2 (en) 2014-10-14 2019-11-26 Applied Materials, Inc. Systems and methods for internal surface conditioning assessment in plasma processing equipment
US10497573B2 (en) 2018-03-13 2019-12-03 Applied Materials, Inc. Selective atomic layer etching of semiconductor materials
US10504700B2 (en) 2015-08-27 2019-12-10 Applied Materials, Inc. Plasma etching systems and methods with secondary plasma injection
US10504754B2 (en) 2016-05-19 2019-12-10 Applied Materials, Inc. Systems and methods for improved semiconductor etching and component protection
US10522371B2 (en) 2016-05-19 2019-12-31 Applied Materials, Inc. Systems and methods for improved semiconductor etching and component protection
US10541184B2 (en) 2017-07-11 2020-01-21 Applied Materials, Inc. Optical emission spectroscopic techniques for monitoring etching
US10541246B2 (en) 2017-06-26 2020-01-21 Applied Materials, Inc. 3D flash memory cells which discourage cross-cell electrical tunneling
US10546729B2 (en) 2016-10-04 2020-01-28 Applied Materials, Inc. Dual-channel showerhead with improved profile
US10566206B2 (en) 2016-12-27 2020-02-18 Applied Materials, Inc. Systems and methods for anisotropic material breakthrough
US10573496B2 (en) 2014-12-09 2020-02-25 Applied Materials, Inc. Direct outlet toroidal plasma source
US10573527B2 (en) 2018-04-06 2020-02-25 Applied Materials, Inc. Gas-phase selective etching systems and methods
US10593560B2 (en) 2018-03-01 2020-03-17 Applied Materials, Inc. Magnetic induction plasma source for semiconductor processes and equipment
US10593523B2 (en) 2014-10-14 2020-03-17 Applied Materials, Inc. Systems and methods for internal surface conditioning in plasma processing equipment
US10615047B2 (en) 2018-02-28 2020-04-07 Applied Materials, Inc. Systems and methods to form airgaps
US10629473B2 (en) 2016-09-09 2020-04-21 Applied Materials, Inc. Footing removal for nitride spacer
US10672642B2 (en) 2018-07-24 2020-06-02 Applied Materials, Inc. Systems and methods for pedestal configuration
US10679870B2 (en) 2018-02-15 2020-06-09 Applied Materials, Inc. Semiconductor processing chamber multistage mixing apparatus
US10699879B2 (en) 2018-04-17 2020-06-30 Applied Materials, Inc. Two piece electrode assembly with gap for plasma control
US10727080B2 (en) 2017-07-07 2020-07-28 Applied Materials, Inc. Tantalum-containing material removal
US10755941B2 (en) 2018-07-06 2020-08-25 Applied Materials, Inc. Self-limiting selective etching systems and methods
US10854426B2 (en) 2018-01-08 2020-12-01 Applied Materials, Inc. Metal recess for semiconductor structures
US10872778B2 (en) 2018-07-06 2020-12-22 Applied Materials, Inc. Systems and methods utilizing solid-phase etchants
US10886137B2 (en) 2018-04-30 2021-01-05 Applied Materials, Inc. Selective nitride removal
US10892198B2 (en) 2018-09-14 2021-01-12 Applied Materials, Inc. Systems and methods for improved performance in semiconductor processing
US10903054B2 (en) 2017-12-19 2021-01-26 Applied Materials, Inc. Multi-zone gas distribution systems and methods
US10920320B2 (en) 2017-06-16 2021-02-16 Applied Materials, Inc. Plasma health determination in semiconductor substrate processing reactors
US10920319B2 (en) 2019-01-11 2021-02-16 Applied Materials, Inc. Ceramic showerheads with conductive electrodes
US10943834B2 (en) 2017-03-13 2021-03-09 Applied Materials, Inc. Replacement contact process
US10964512B2 (en) 2018-02-15 2021-03-30 Applied Materials, Inc. Semiconductor processing chamber multistage mixing apparatus and methods
US11024486B2 (en) 2013-02-08 2021-06-01 Applied Materials, Inc. Semiconductor processing systems having multiple plasma configurations
US11049755B2 (en) 2018-09-14 2021-06-29 Applied Materials, Inc. Semiconductor substrate supports with embedded RF shield
US11062887B2 (en) 2018-09-17 2021-07-13 Applied Materials, Inc. High temperature RF heater pedestals
US11121002B2 (en) 2018-10-24 2021-09-14 Applied Materials, Inc. Systems and methods for etching metals and metal derivatives
US11239061B2 (en) 2014-11-26 2022-02-01 Applied Materials, Inc. Methods and systems to enhance process uniformity
US11257693B2 (en) 2015-01-09 2022-02-22 Applied Materials, Inc. Methods and systems to improve pedestal temperature control
US11276590B2 (en) 2017-05-17 2022-03-15 Applied Materials, Inc. Multi-zone semiconductor substrate supports
US11276559B2 (en) 2017-05-17 2022-03-15 Applied Materials, Inc. Semiconductor processing chamber for multiple precursor flow
US11328909B2 (en) 2017-12-22 2022-05-10 Applied Materials, Inc. Chamber conditioning and removal processes
US11417534B2 (en) 2018-09-21 2022-08-16 Applied Materials, Inc. Selective material removal
US11437242B2 (en) 2018-11-27 2022-09-06 Applied Materials, Inc. Selective removal of silicon-containing materials
US11594428B2 (en) 2015-02-03 2023-02-28 Applied Materials, Inc. Low temperature chuck for plasma processing systems
US11682560B2 (en) 2018-10-11 2023-06-20 Applied Materials, Inc. Systems and methods for hafnium-containing film removal
US11721527B2 (en) 2019-01-07 2023-08-08 Applied Materials, Inc. Processing chamber mixing systems
WO2023215398A1 (en) * 2022-05-06 2023-11-09 Applied Materials, Inc. Pulsed etch process

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8183161B2 (en) * 2006-09-12 2012-05-22 Tokyo Electron Limited Method and system for dry etching a hafnium containing material
US7521369B2 (en) * 2006-10-23 2009-04-21 Interuniversitair Microelektronica Centrum (Imec) Selective removal of rare earth based high-k materials in a semiconductor device
JP4849614B2 (en) 2006-11-01 2012-01-11 東京エレクトロン株式会社 Substrate processing method and substrate processing system
US8221636B2 (en) * 2008-05-12 2012-07-17 Headway Technologies, Inc. Method of manufacturing magnetic head for perpendicular magnetic recording
KR101190891B1 (en) * 2008-12-17 2012-10-12 파나소닉 주식회사 Method for forming through electrode, and semiconductor device
US8313661B2 (en) * 2009-11-09 2012-11-20 Tokyo Electron Limited Deep trench liner removal process
JP6163446B2 (en) 2014-03-27 2017-07-12 株式会社東芝 Manufacturing method of semiconductor device
JP6454492B2 (en) * 2014-08-08 2019-01-16 東京エレクトロン株式会社 Method for etching a multilayer film

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3878084A (en) * 1973-05-25 1975-04-15 Hooker Chemicals Plastics Corp Bipolar electrode
US5527425A (en) * 1995-07-21 1996-06-18 At&T Corp. Method of making in-containing III/V semiconductor devices
US20010055852A1 (en) * 1998-09-09 2001-12-27 Moise Theodore S. Integrated circuit and method
US6350665B1 (en) * 2000-04-28 2002-02-26 Cypress Semiconductor Corporation Semiconductor structure and method of making contacts and source and/or drain junctions in a semiconductor device
US6399508B1 (en) * 1999-01-12 2002-06-04 Applied Materials, Inc. Method for metal etch using a dielectric hard mask
US20020079057A1 (en) * 1999-10-08 2002-06-27 Ken Yoshioka Apparatus for processing specimens
US6436838B1 (en) * 2000-04-21 2002-08-20 Applied Materials, Inc. Method of patterning lead zirconium titanate and barium strontium titanate
US20030036264A1 (en) * 2001-07-06 2003-02-20 Chentsau Ying Method of etching platinum using a silicon carbide mask

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5314576A (en) * 1992-06-09 1994-05-24 Sony Corporation Dry etching method using (SN)x protective layer
TW451344B (en) * 2000-03-15 2001-08-21 Winbond Electronics Corp Profile controlling method to etch metal layer
EP1137058A1 (en) * 2000-03-23 2001-09-26 Motorola, Inc. A method for pattering layers of semiconductor devices
JP4182467B2 (en) * 2001-12-27 2008-11-19 セイコーエプソン株式会社 Circuit board, electro-optical device and electronic apparatus
US20030143853A1 (en) 2002-01-31 2003-07-31 Celii Francis G. FeRAM capacitor stack etch
US6770506B2 (en) * 2002-12-23 2004-08-03 Motorola, Inc. Release etch method for micromachined sensors
JP4282391B2 (en) * 2003-07-09 2009-06-17 Necエレクトロニクス株式会社 Manufacturing method of semiconductor device
US7119032B2 (en) * 2004-08-23 2006-10-10 Air Products And Chemicals, Inc. Method to protect internal components of semiconductor processing equipment using layered superlattice materials

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3878084A (en) * 1973-05-25 1975-04-15 Hooker Chemicals Plastics Corp Bipolar electrode
US5527425A (en) * 1995-07-21 1996-06-18 At&T Corp. Method of making in-containing III/V semiconductor devices
US20010055852A1 (en) * 1998-09-09 2001-12-27 Moise Theodore S. Integrated circuit and method
US6399508B1 (en) * 1999-01-12 2002-06-04 Applied Materials, Inc. Method for metal etch using a dielectric hard mask
US20020079057A1 (en) * 1999-10-08 2002-06-27 Ken Yoshioka Apparatus for processing specimens
US6436838B1 (en) * 2000-04-21 2002-08-20 Applied Materials, Inc. Method of patterning lead zirconium titanate and barium strontium titanate
US6350665B1 (en) * 2000-04-28 2002-02-26 Cypress Semiconductor Corporation Semiconductor structure and method of making contacts and source and/or drain junctions in a semiconductor device
US20030036264A1 (en) * 2001-07-06 2003-02-20 Chentsau Ying Method of etching platinum using a silicon carbide mask

Cited By (205)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8466023B2 (en) 2009-10-19 2013-06-18 Samsung Electronics Co., Ltd. Semiconductor device and method for fabricating the same
US9419072B2 (en) 2009-10-19 2016-08-16 Samsung Electronics Co., Ltd. Semiconductor device and method for fabricating the same
US20110092040A1 (en) * 2009-10-19 2011-04-21 Samsung Electronics Co., Ltd. Semiconductor device and method for fabricating the same
US9608054B2 (en) 2009-10-19 2017-03-28 Samsung Electronics Co., Ltd. Semiconductor device and method for fabricating the same
US9754800B2 (en) 2010-05-27 2017-09-05 Applied Materials, Inc. Selective etch for silicon films
US9324576B2 (en) 2010-05-27 2016-04-26 Applied Materials, Inc. Selective etch for silicon films
US10283321B2 (en) 2011-01-18 2019-05-07 Applied Materials, Inc. Semiconductor processing system and methods using capacitively coupled plasma
US10062578B2 (en) 2011-03-14 2018-08-28 Applied Materials, Inc. Methods for etch of metal and metal-oxide films
US9842744B2 (en) 2011-03-14 2017-12-12 Applied Materials, Inc. Methods for etch of SiN films
US9236266B2 (en) 2011-08-01 2016-01-12 Applied Materials, Inc. Dry-etch for silicon-and-carbon-containing films
US8927390B2 (en) 2011-09-26 2015-01-06 Applied Materials, Inc. Intrench profile
US9012302B2 (en) 2011-09-26 2015-04-21 Applied Materials, Inc. Intrench profile
US9418858B2 (en) 2011-10-07 2016-08-16 Applied Materials, Inc. Selective etch of silicon by way of metastable hydrogen termination
US10062587B2 (en) 2012-07-18 2018-08-28 Applied Materials, Inc. Pedestal with multi-zone temperature control and multiple purge capabilities
US9373517B2 (en) 2012-08-02 2016-06-21 Applied Materials, Inc. Semiconductor processing with DC assisted RF power for improved control
US10032606B2 (en) 2012-08-02 2018-07-24 Applied Materials, Inc. Semiconductor processing with DC assisted RF power for improved control
US9887096B2 (en) 2012-09-17 2018-02-06 Applied Materials, Inc. Differential silicon oxide etch
US9437451B2 (en) 2012-09-18 2016-09-06 Applied Materials, Inc. Radical-component oxide etch
US9390937B2 (en) 2012-09-20 2016-07-12 Applied Materials, Inc. Silicon-carbon-nitride selective etch
US11264213B2 (en) 2012-09-21 2022-03-01 Applied Materials, Inc. Chemical control features in wafer process equipment
US10354843B2 (en) 2012-09-21 2019-07-16 Applied Materials, Inc. Chemical control features in wafer process equipment
US9132436B2 (en) 2012-09-21 2015-09-15 Applied Materials, Inc. Chemical control features in wafer process equipment
US9978564B2 (en) 2012-09-21 2018-05-22 Applied Materials, Inc. Chemical control features in wafer process equipment
US9384997B2 (en) 2012-11-20 2016-07-05 Applied Materials, Inc. Dry-etch selectivity
US9412608B2 (en) 2012-11-30 2016-08-09 Applied Materials, Inc. Dry-etch for selective tungsten removal
US9355863B2 (en) 2012-12-18 2016-05-31 Applied Materials, Inc. Non-local plasma oxide etch
US9449845B2 (en) 2012-12-21 2016-09-20 Applied Materials, Inc. Selective titanium nitride etching
US11024486B2 (en) 2013-02-08 2021-06-01 Applied Materials, Inc. Semiconductor processing systems having multiple plasma configurations
US10424485B2 (en) 2013-03-01 2019-09-24 Applied Materials, Inc. Enhanced etching processes using remote plasma sources
US9362130B2 (en) 2013-03-01 2016-06-07 Applied Materials, Inc. Enhanced etching processes using remote plasma sources
US9607856B2 (en) 2013-03-05 2017-03-28 Applied Materials, Inc. Selective titanium nitride removal
US9040422B2 (en) * 2013-03-05 2015-05-26 Applied Materials, Inc. Selective titanium nitride removal
US9093390B2 (en) 2013-03-07 2015-07-28 Applied Materials, Inc. Conformal oxide dry etch
US10170282B2 (en) 2013-03-08 2019-01-01 Applied Materials, Inc. Insulated semiconductor faceplate designs
US9991134B2 (en) 2013-03-15 2018-06-05 Applied Materials, Inc. Processing systems and methods for halide scavenging
US9449850B2 (en) 2013-03-15 2016-09-20 Applied Materials, Inc. Processing systems and methods for halide scavenging
US9093371B2 (en) 2013-03-15 2015-07-28 Applied Materials, Inc. Processing systems and methods for halide scavenging
US9184055B2 (en) 2013-03-15 2015-11-10 Applied Materials, Inc. Processing systems and methods for halide scavenging
US9659792B2 (en) 2013-03-15 2017-05-23 Applied Materials, Inc. Processing systems and methods for halide scavenging
US9704723B2 (en) 2013-03-15 2017-07-11 Applied Materials, Inc. Processing systems and methods for halide scavenging
US9023732B2 (en) 2013-03-15 2015-05-05 Applied Materials, Inc. Processing systems and methods for halide scavenging
US9153442B2 (en) 2013-03-15 2015-10-06 Applied Materials, Inc. Processing systems and methods for halide scavenging
US8895449B1 (en) 2013-05-16 2014-11-25 Applied Materials, Inc. Delicate dry clean
US9114438B2 (en) 2013-05-21 2015-08-25 Applied Materials, Inc. Copper residue chamber clean
US9493879B2 (en) 2013-07-12 2016-11-15 Applied Materials, Inc. Selective sputtering for pattern transfer
US9773648B2 (en) 2013-08-30 2017-09-26 Applied Materials, Inc. Dual discharge modes operation for remote plasma
US8956980B1 (en) 2013-09-16 2015-02-17 Applied Materials, Inc. Selective etch of silicon nitride
US9209012B2 (en) 2013-09-16 2015-12-08 Applied Materials, Inc. Selective etch of silicon nitride
US8951429B1 (en) 2013-10-29 2015-02-10 Applied Materials, Inc. Tungsten oxide processing
US9576809B2 (en) 2013-11-04 2017-02-21 Applied Materials, Inc. Etch suppression with germanium
US9236265B2 (en) 2013-11-04 2016-01-12 Applied Materials, Inc. Silicon germanium processing
US9520303B2 (en) 2013-11-12 2016-12-13 Applied Materials, Inc. Aluminum selective etch
US9711366B2 (en) 2013-11-12 2017-07-18 Applied Materials, Inc. Selective etch for metal-containing materials
US9472417B2 (en) 2013-11-12 2016-10-18 Applied Materials, Inc. Plasma-free metal etch
US9472412B2 (en) 2013-12-02 2016-10-18 Applied Materials, Inc. Procedure for etch rate consistency
US9245762B2 (en) 2013-12-02 2016-01-26 Applied Materials, Inc. Procedure for etch rate consistency
US9117855B2 (en) 2013-12-04 2015-08-25 Applied Materials, Inc. Polarity control for remote plasma
US9287095B2 (en) 2013-12-17 2016-03-15 Applied Materials, Inc. Semiconductor system assemblies and methods of operation
US9263278B2 (en) 2013-12-17 2016-02-16 Applied Materials, Inc. Dopant etch selectivity control
US9190293B2 (en) 2013-12-18 2015-11-17 Applied Materials, Inc. Even tungsten etch for high aspect ratio trenches
US9287134B2 (en) 2014-01-17 2016-03-15 Applied Materials, Inc. Titanium oxide etch
US9293568B2 (en) 2014-01-27 2016-03-22 Applied Materials, Inc. Method of fin patterning
US9396989B2 (en) 2014-01-27 2016-07-19 Applied Materials, Inc. Air gaps between copper lines
US9385028B2 (en) 2014-02-03 2016-07-05 Applied Materials, Inc. Air gap process
US9499898B2 (en) 2014-03-03 2016-11-22 Applied Materials, Inc. Layered thin film heater and method of fabrication
US9299575B2 (en) 2014-03-17 2016-03-29 Applied Materials, Inc. Gas-phase tungsten etch
US9837249B2 (en) 2014-03-20 2017-12-05 Applied Materials, Inc. Radial waveguide systems and methods for post-match control of microwaves
US9299537B2 (en) 2014-03-20 2016-03-29 Applied Materials, Inc. Radial waveguide systems and methods for post-match control of microwaves
US9564296B2 (en) 2014-03-20 2017-02-07 Applied Materials, Inc. Radial waveguide systems and methods for post-match control of microwaves
US9299538B2 (en) 2014-03-20 2016-03-29 Applied Materials, Inc. Radial waveguide systems and methods for post-match control of microwaves
US9136273B1 (en) 2014-03-21 2015-09-15 Applied Materials, Inc. Flash gate air gap
US9903020B2 (en) 2014-03-31 2018-02-27 Applied Materials, Inc. Generation of compact alumina passivation layers on aluminum plasma equipment components
US9885117B2 (en) 2014-03-31 2018-02-06 Applied Materials, Inc. Conditioned semiconductor system parts
US9269590B2 (en) 2014-04-07 2016-02-23 Applied Materials, Inc. Spacer formation
US10465294B2 (en) 2014-05-28 2019-11-05 Applied Materials, Inc. Oxide and metal removal
US9309598B2 (en) 2014-05-28 2016-04-12 Applied Materials, Inc. Oxide and metal removal
US9847289B2 (en) 2014-05-30 2017-12-19 Applied Materials, Inc. Protective via cap for improved interconnect performance
US9406523B2 (en) 2014-06-19 2016-08-02 Applied Materials, Inc. Highly selective doped oxide removal method
US9378969B2 (en) 2014-06-19 2016-06-28 Applied Materials, Inc. Low temperature gas-phase carbon removal
US9425058B2 (en) 2014-07-24 2016-08-23 Applied Materials, Inc. Simplified litho-etch-litho-etch process
US9773695B2 (en) 2014-07-31 2017-09-26 Applied Materials, Inc. Integrated bit-line airgap formation and gate stack post clean
US9378978B2 (en) 2014-07-31 2016-06-28 Applied Materials, Inc. Integrated oxide recess and floating gate fin trimming
US9159606B1 (en) 2014-07-31 2015-10-13 Applied Materials, Inc. Metal air gap
US9496167B2 (en) 2014-07-31 2016-11-15 Applied Materials, Inc. Integrated bit-line airgap formation and gate stack post clean
US9165786B1 (en) 2014-08-05 2015-10-20 Applied Materials, Inc. Integrated oxide and nitride recess for better channel contact in 3D architectures
US9659753B2 (en) 2014-08-07 2017-05-23 Applied Materials, Inc. Grooved insulator to reduce leakage current
US9553102B2 (en) 2014-08-19 2017-01-24 Applied Materials, Inc. Tungsten separation
US9355856B2 (en) 2014-09-12 2016-05-31 Applied Materials, Inc. V trench dry etch
US9355862B2 (en) 2014-09-24 2016-05-31 Applied Materials, Inc. Fluorine-based hardmask removal
US9368364B2 (en) 2014-09-24 2016-06-14 Applied Materials, Inc. Silicon etch process with tunable selectivity to SiO2 and other materials
US9478434B2 (en) 2014-09-24 2016-10-25 Applied Materials, Inc. Chlorine-based hardmask removal
US9613822B2 (en) 2014-09-25 2017-04-04 Applied Materials, Inc. Oxide etch selectivity enhancement
US9837284B2 (en) 2014-09-25 2017-12-05 Applied Materials, Inc. Oxide etch selectivity enhancement
US9478432B2 (en) 2014-09-25 2016-10-25 Applied Materials, Inc. Silicon oxide selective removal
US10707061B2 (en) 2014-10-14 2020-07-07 Applied Materials, Inc. Systems and methods for internal surface conditioning in plasma processing equipment
US10593523B2 (en) 2014-10-14 2020-03-17 Applied Materials, Inc. Systems and methods for internal surface conditioning in plasma processing equipment
US10490418B2 (en) 2014-10-14 2019-11-26 Applied Materials, Inc. Systems and methods for internal surface conditioning assessment in plasma processing equipment
US10796922B2 (en) 2014-10-14 2020-10-06 Applied Materials, Inc. Systems and methods for internal surface conditioning assessment in plasma processing equipment
US11637002B2 (en) 2014-11-26 2023-04-25 Applied Materials, Inc. Methods and systems to enhance process uniformity
US11239061B2 (en) 2014-11-26 2022-02-01 Applied Materials, Inc. Methods and systems to enhance process uniformity
US9299583B1 (en) 2014-12-05 2016-03-29 Applied Materials, Inc. Aluminum oxide selective etch
US10573496B2 (en) 2014-12-09 2020-02-25 Applied Materials, Inc. Direct outlet toroidal plasma source
US10224210B2 (en) 2014-12-09 2019-03-05 Applied Materials, Inc. Plasma processing system with direct outlet toroidal plasma source
US9502258B2 (en) 2014-12-23 2016-11-22 Applied Materials, Inc. Anisotropic gap etch
US9343272B1 (en) 2015-01-08 2016-05-17 Applied Materials, Inc. Self-aligned process
US11257693B2 (en) 2015-01-09 2022-02-22 Applied Materials, Inc. Methods and systems to improve pedestal temperature control
US9373522B1 (en) 2015-01-22 2016-06-21 Applied Mateials, Inc. Titanium nitride removal
US9449846B2 (en) 2015-01-28 2016-09-20 Applied Materials, Inc. Vertical gate separation
US9728437B2 (en) 2015-02-03 2017-08-08 Applied Materials, Inc. High temperature chuck for plasma processing systems
US11594428B2 (en) 2015-02-03 2023-02-28 Applied Materials, Inc. Low temperature chuck for plasma processing systems
US10468285B2 (en) 2015-02-03 2019-11-05 Applied Materials, Inc. High temperature chuck for plasma processing systems
US9881805B2 (en) 2015-03-02 2018-01-30 Applied Materials, Inc. Silicon selective removal
US9741593B2 (en) 2015-08-06 2017-08-22 Applied Materials, Inc. Thermal management systems and methods for wafer processing systems
US9691645B2 (en) 2015-08-06 2017-06-27 Applied Materials, Inc. Bolted wafer chuck thermal management systems and methods for wafer processing systems
US10147620B2 (en) 2015-08-06 2018-12-04 Applied Materials, Inc. Bolted wafer chuck thermal management systems and methods for wafer processing systems
US10607867B2 (en) 2015-08-06 2020-03-31 Applied Materials, Inc. Bolted wafer chuck thermal management systems and methods for wafer processing systems
US11158527B2 (en) 2015-08-06 2021-10-26 Applied Materials, Inc. Thermal management systems and methods for wafer processing systems
US10468276B2 (en) 2015-08-06 2019-11-05 Applied Materials, Inc. Thermal management systems and methods for wafer processing systems
US9349605B1 (en) 2015-08-07 2016-05-24 Applied Materials, Inc. Oxide etch selectivity systems and methods
US10424464B2 (en) 2015-08-07 2019-09-24 Applied Materials, Inc. Oxide etch selectivity systems and methods
US10424463B2 (en) 2015-08-07 2019-09-24 Applied Materials, Inc. Oxide etch selectivity systems and methods
US10504700B2 (en) 2015-08-27 2019-12-10 Applied Materials, Inc. Plasma etching systems and methods with secondary plasma injection
US11476093B2 (en) 2015-08-27 2022-10-18 Applied Materials, Inc. Plasma etching systems and methods with secondary plasma injection
US10522371B2 (en) 2016-05-19 2019-12-31 Applied Materials, Inc. Systems and methods for improved semiconductor etching and component protection
US10504754B2 (en) 2016-05-19 2019-12-10 Applied Materials, Inc. Systems and methods for improved semiconductor etching and component protection
US11735441B2 (en) 2016-05-19 2023-08-22 Applied Materials, Inc. Systems and methods for improved semiconductor etching and component protection
US9865484B1 (en) 2016-06-29 2018-01-09 Applied Materials, Inc. Selective etch using material modification and RF pulsing
US10629473B2 (en) 2016-09-09 2020-04-21 Applied Materials, Inc. Footing removal for nitride spacer
US10062575B2 (en) 2016-09-09 2018-08-28 Applied Materials, Inc. Poly directional etch by oxidation
US10224180B2 (en) 2016-10-04 2019-03-05 Applied Materials, Inc. Chamber with flow-through source
US9721789B1 (en) 2016-10-04 2017-08-01 Applied Materials, Inc. Saving ion-damaged spacers
US10546729B2 (en) 2016-10-04 2020-01-28 Applied Materials, Inc. Dual-channel showerhead with improved profile
US10541113B2 (en) 2016-10-04 2020-01-21 Applied Materials, Inc. Chamber with flow-through source
US11049698B2 (en) 2016-10-04 2021-06-29 Applied Materials, Inc. Dual-channel showerhead with improved profile
US9934942B1 (en) 2016-10-04 2018-04-03 Applied Materials, Inc. Chamber with flow-through source
US10062585B2 (en) 2016-10-04 2018-08-28 Applied Materials, Inc. Oxygen compatible plasma source
US10319603B2 (en) 2016-10-07 2019-06-11 Applied Materials, Inc. Selective SiN lateral recess
US10062579B2 (en) 2016-10-07 2018-08-28 Applied Materials, Inc. Selective SiN lateral recess
US9947549B1 (en) 2016-10-10 2018-04-17 Applied Materials, Inc. Cobalt-containing material removal
US10163696B2 (en) 2016-11-11 2018-12-25 Applied Materials, Inc. Selective cobalt removal for bottom up gapfill
US10770346B2 (en) 2016-11-11 2020-09-08 Applied Materials, Inc. Selective cobalt removal for bottom up gapfill
US10186428B2 (en) 2016-11-11 2019-01-22 Applied Materials, Inc. Removal methods for high aspect ratio structures
US9768034B1 (en) 2016-11-11 2017-09-19 Applied Materials, Inc. Removal methods for high aspect ratio structures
US10600639B2 (en) 2016-11-14 2020-03-24 Applied Materials, Inc. SiN spacer profile patterning
US10026621B2 (en) 2016-11-14 2018-07-17 Applied Materials, Inc. SiN spacer profile patterning
US10242908B2 (en) 2016-11-14 2019-03-26 Applied Materials, Inc. Airgap formation with damage-free copper
US10566206B2 (en) 2016-12-27 2020-02-18 Applied Materials, Inc. Systems and methods for anisotropic material breakthrough
US10403507B2 (en) 2017-02-03 2019-09-03 Applied Materials, Inc. Shaped etch profile with oxidation
US10903052B2 (en) 2017-02-03 2021-01-26 Applied Materials, Inc. Systems and methods for radial and azimuthal control of plasma uniformity
US10431429B2 (en) 2017-02-03 2019-10-01 Applied Materials, Inc. Systems and methods for radial and azimuthal control of plasma uniformity
US10043684B1 (en) 2017-02-06 2018-08-07 Applied Materials, Inc. Self-limiting atomic thermal etching systems and methods
US10529737B2 (en) 2017-02-08 2020-01-07 Applied Materials, Inc. Accommodating imperfectly aligned memory holes
US10325923B2 (en) 2017-02-08 2019-06-18 Applied Materials, Inc. Accommodating imperfectly aligned memory holes
US10319739B2 (en) 2017-02-08 2019-06-11 Applied Materials, Inc. Accommodating imperfectly aligned memory holes
US10943834B2 (en) 2017-03-13 2021-03-09 Applied Materials, Inc. Replacement contact process
US10319649B2 (en) 2017-04-11 2019-06-11 Applied Materials, Inc. Optical emission spectroscopy (OES) for remote plasma monitoring
US11276559B2 (en) 2017-05-17 2022-03-15 Applied Materials, Inc. Semiconductor processing chamber for multiple precursor flow
US11915950B2 (en) 2017-05-17 2024-02-27 Applied Materials, Inc. Multi-zone semiconductor substrate supports
US11276590B2 (en) 2017-05-17 2022-03-15 Applied Materials, Inc. Multi-zone semiconductor substrate supports
US11361939B2 (en) 2017-05-17 2022-06-14 Applied Materials, Inc. Semiconductor processing chamber for multiple precursor flow
US10049891B1 (en) 2017-05-31 2018-08-14 Applied Materials, Inc. Selective in situ cobalt residue removal
US10468267B2 (en) 2017-05-31 2019-11-05 Applied Materials, Inc. Water-free etching methods
US10497579B2 (en) 2017-05-31 2019-12-03 Applied Materials, Inc. Water-free etching methods
US10920320B2 (en) 2017-06-16 2021-02-16 Applied Materials, Inc. Plasma health determination in semiconductor substrate processing reactors
US10541246B2 (en) 2017-06-26 2020-01-21 Applied Materials, Inc. 3D flash memory cells which discourage cross-cell electrical tunneling
US10727080B2 (en) 2017-07-07 2020-07-28 Applied Materials, Inc. Tantalum-containing material removal
US10541184B2 (en) 2017-07-11 2020-01-21 Applied Materials, Inc. Optical emission spectroscopic techniques for monitoring etching
US10354889B2 (en) 2017-07-17 2019-07-16 Applied Materials, Inc. Non-halogen etching of silicon-containing materials
US10593553B2 (en) 2017-08-04 2020-03-17 Applied Materials, Inc. Germanium etching systems and methods
US10170336B1 (en) 2017-08-04 2019-01-01 Applied Materials, Inc. Methods for anisotropic control of selective silicon removal
US10043674B1 (en) 2017-08-04 2018-08-07 Applied Materials, Inc. Germanium etching systems and methods
US11101136B2 (en) 2017-08-07 2021-08-24 Applied Materials, Inc. Process window widening using coated parts in plasma etch processes
US10297458B2 (en) 2017-08-07 2019-05-21 Applied Materials, Inc. Process window widening using coated parts in plasma etch processes
US10283324B1 (en) 2017-10-24 2019-05-07 Applied Materials, Inc. Oxygen treatment for nitride etching
US10128086B1 (en) 2017-10-24 2018-11-13 Applied Materials, Inc. Silicon pretreatment for nitride removal
US10256112B1 (en) 2017-12-08 2019-04-09 Applied Materials, Inc. Selective tungsten removal
US10903054B2 (en) 2017-12-19 2021-01-26 Applied Materials, Inc. Multi-zone gas distribution systems and methods
US11328909B2 (en) 2017-12-22 2022-05-10 Applied Materials, Inc. Chamber conditioning and removal processes
US10861676B2 (en) 2018-01-08 2020-12-08 Applied Materials, Inc. Metal recess for semiconductor structures
US10854426B2 (en) 2018-01-08 2020-12-01 Applied Materials, Inc. Metal recess for semiconductor structures
US10679870B2 (en) 2018-02-15 2020-06-09 Applied Materials, Inc. Semiconductor processing chamber multistage mixing apparatus
US10964512B2 (en) 2018-02-15 2021-03-30 Applied Materials, Inc. Semiconductor processing chamber multistage mixing apparatus and methods
US10699921B2 (en) 2018-02-15 2020-06-30 Applied Materials, Inc. Semiconductor processing chamber multistage mixing apparatus
US10615047B2 (en) 2018-02-28 2020-04-07 Applied Materials, Inc. Systems and methods to form airgaps
US10593560B2 (en) 2018-03-01 2020-03-17 Applied Materials, Inc. Magnetic induction plasma source for semiconductor processes and equipment
US10319600B1 (en) 2018-03-12 2019-06-11 Applied Materials, Inc. Thermal silicon etch
US11004689B2 (en) 2018-03-12 2021-05-11 Applied Materials, Inc. Thermal silicon etch
US10497573B2 (en) 2018-03-13 2019-12-03 Applied Materials, Inc. Selective atomic layer etching of semiconductor materials
US10573527B2 (en) 2018-04-06 2020-02-25 Applied Materials, Inc. Gas-phase selective etching systems and methods
US10490406B2 (en) 2018-04-10 2019-11-26 Appled Materials, Inc. Systems and methods for material breakthrough
US10699879B2 (en) 2018-04-17 2020-06-30 Applied Materials, Inc. Two piece electrode assembly with gap for plasma control
US10886137B2 (en) 2018-04-30 2021-01-05 Applied Materials, Inc. Selective nitride removal
US10755941B2 (en) 2018-07-06 2020-08-25 Applied Materials, Inc. Self-limiting selective etching systems and methods
US10872778B2 (en) 2018-07-06 2020-12-22 Applied Materials, Inc. Systems and methods utilizing solid-phase etchants
US10672642B2 (en) 2018-07-24 2020-06-02 Applied Materials, Inc. Systems and methods for pedestal configuration
US10892198B2 (en) 2018-09-14 2021-01-12 Applied Materials, Inc. Systems and methods for improved performance in semiconductor processing
US11049755B2 (en) 2018-09-14 2021-06-29 Applied Materials, Inc. Semiconductor substrate supports with embedded RF shield
US11062887B2 (en) 2018-09-17 2021-07-13 Applied Materials, Inc. High temperature RF heater pedestals
US11417534B2 (en) 2018-09-21 2022-08-16 Applied Materials, Inc. Selective material removal
US11682560B2 (en) 2018-10-11 2023-06-20 Applied Materials, Inc. Systems and methods for hafnium-containing film removal
US11121002B2 (en) 2018-10-24 2021-09-14 Applied Materials, Inc. Systems and methods for etching metals and metal derivatives
US11437242B2 (en) 2018-11-27 2022-09-06 Applied Materials, Inc. Selective removal of silicon-containing materials
US11721527B2 (en) 2019-01-07 2023-08-08 Applied Materials, Inc. Processing chamber mixing systems
US10920319B2 (en) 2019-01-11 2021-02-16 Applied Materials, Inc. Ceramic showerheads with conductive electrodes
WO2023215398A1 (en) * 2022-05-06 2023-11-09 Applied Materials, Inc. Pulsed etch process

Also Published As

Publication number Publication date
JP5328094B2 (en) 2013-10-30
EP1780779A3 (en) 2008-06-11
EP1780780A3 (en) 2008-12-17
EP1780780A2 (en) 2007-05-02
EP1780779A2 (en) 2007-05-02
JP2007123903A (en) 2007-05-17
US20070099403A1 (en) 2007-05-03
US7598184B2 (en) 2009-10-06

Similar Documents

Publication Publication Date Title
US20070099428A1 (en) Plasma for patterning advanced gate stacks
TWI352387B (en) Etch methods to form anisotropic features for high
US9005473B2 (en) Gaseous compositions comprising hydrogen fluoride and an alkylated ammonia derivative
US7132370B2 (en) Method for selective removal of high-k material
US20050106888A1 (en) Method of in-situ damage removal - post O2 dry process
US20060199370A1 (en) Method of in-situ ash strip to eliminate memory effect and reduce wafer damage
KR100238691B1 (en) Dry etching method
EP2179439A1 (en) Methods of smoothing oxide spacer
US6875664B1 (en) Formation of amorphous carbon ARC stack having graded transition between amorphous carbon and ARC material
CN117203741A (en) Plasma etching technique
JP5250476B2 (en) Dry etching method
US6933243B2 (en) High selectivity and residue free process for metal on thin dielectric gate etch application
US7811928B2 (en) Semiconductor devices and fabrication methods thereof
Shin et al. Dry etching of TaN/HfO2 gate stack structure by Cl2/SF6/Ar inductively coupled plasma
US7344965B2 (en) Method of etching dual pre-doped polysilicon gate stacks using carbon-containing gaseous additions
US20100184297A1 (en) Method for protecting semiconductor wafer and process for producing semiconductor device
Maeda et al. Selective dry etching of HfO2 in CF4 and Cl2/HBr-based chemistries
KR100218772B1 (en) Dry etching method
Shamiryan et al. Profile control of novel non-Si gates using B Cl 3∕ N 2 plasma
US11232954B2 (en) Sidewall protection layer formation for substrate processing
JP2007123890A (en) Plasma for patterning improved gate stack
US10699911B2 (en) Method of conformal etching selective to other materials
JPH06349788A (en) Etching method
US20050056615A1 (en) Selective plasma etching process for aluminum oxide patterning
JP3283611B2 (en) Method for manufacturing semiconductor device

Legal Events

Date Code Title Description
AS Assignment

Owner name: INTERUNIVERSITAIR MICROELEKTRONICA CENTRUM (IMEC),

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:SHAMIRYAN, DENIS;PARASCHIV, VASILE;DEMAND, MARC;AND OTHERS;REEL/FRAME:018629/0854;SIGNING DATES FROM 20061113 TO 20061212

AS Assignment

Owner name: IMEC,BELGIUM

Free format text: "IMEC" IS AN ALTERNATIVE OFFICIAL NAME FOR "INTERUNIVERSITAIR MICROELEKTRONICA CENTRUM VZW";ASSIGNOR:INTERUNIVERSITAIR MICROELEKTRONICA CENTRUM VZW;REEL/FRAME:024200/0675

Effective date: 19840318

Owner name: IMEC, BELGIUM

Free format text: "IMEC" IS AN ALTERNATIVE OFFICIAL NAME FOR "INTERUNIVERSITAIR MICROELEKTRONICA CENTRUM VZW";ASSIGNOR:INTERUNIVERSITAIR MICROELEKTRONICA CENTRUM VZW;REEL/FRAME:024200/0675

Effective date: 19840318

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION