US20050189217A1 - Method and apparatus for forming a barrier layer on a substrate - Google Patents
Method and apparatus for forming a barrier layer on a substrate Download PDFInfo
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- US20050189217A1 US20050189217A1 US11/110,608 US11060805A US2005189217A1 US 20050189217 A1 US20050189217 A1 US 20050189217A1 US 11060805 A US11060805 A US 11060805A US 2005189217 A1 US2005189217 A1 US 2005189217A1
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- layer
- tantalum
- sputter
- tantalum nitride
- reactor
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- 239000000758 substrate Substances 0.000 title claims abstract description 44
- 238000000034 method Methods 0.000 title abstract description 39
- 230000004888 barrier function Effects 0.000 title abstract description 23
- MZLGASXMSKOWSE-UHFFFAOYSA-N tantalum nitride Chemical compound [Ta]#N MZLGASXMSKOWSE-UHFFFAOYSA-N 0.000 claims abstract description 72
- 229910052715 tantalum Inorganic materials 0.000 claims abstract description 71
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims abstract description 70
- 229910052751 metal Inorganic materials 0.000 claims abstract description 31
- 239000002184 metal Substances 0.000 claims abstract description 31
- 238000000151 deposition Methods 0.000 claims abstract description 21
- 238000004544 sputter deposition Methods 0.000 claims description 54
- NJPPVKZQTLUDBO-UHFFFAOYSA-N novaluron Chemical compound C1=C(Cl)C(OC(F)(F)C(OC(F)(F)F)F)=CC=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F NJPPVKZQTLUDBO-UHFFFAOYSA-N 0.000 claims description 38
- 238000005240 physical vapour deposition Methods 0.000 claims description 10
- 150000002500 ions Chemical class 0.000 claims description 9
- 238000002294 plasma sputter deposition Methods 0.000 claims description 8
- 238000005477 sputtering target Methods 0.000 claims description 4
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 24
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 24
- 230000009977 dual effect Effects 0.000 description 17
- 235000012431 wafers Nutrition 0.000 description 16
- 229910052786 argon Inorganic materials 0.000 description 13
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 12
- 239000010949 copper Substances 0.000 description 12
- 229910052802 copper Inorganic materials 0.000 description 12
- 239000007789 gas Substances 0.000 description 12
- 229910052757 nitrogen Inorganic materials 0.000 description 11
- 239000000463 material Substances 0.000 description 9
- 229910021645 metal ion Inorganic materials 0.000 description 7
- 239000004065 semiconductor Substances 0.000 description 6
- 238000004590 computer program Methods 0.000 description 5
- 230000008021 deposition Effects 0.000 description 4
- 238000005546 reactive sputtering Methods 0.000 description 4
- 238000009792 diffusion process Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 150000004767 nitrides Chemical class 0.000 description 3
- 238000009736 wetting Methods 0.000 description 3
- -1 argon ions Chemical class 0.000 description 2
- 239000003990 capacitor Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 238000004070 electrodeposition Methods 0.000 description 2
- 238000001465 metallisation Methods 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 230000001902 propagating effect Effects 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 238000001552 radio frequency sputter deposition Methods 0.000 description 1
- 238000005389 semiconductor device fabrication Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000013077 target material Substances 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
Images
Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76838—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
- H01L21/76841—Barrier, adhesion or liner layers
- H01L21/76843—Barrier, adhesion or liner layers formed in openings in a dielectric
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/04—Coating on selected surface areas, e.g. using masks
- C23C14/046—Coating cavities or hollow spaces, e.g. interior of tubes; Infiltration of porous substrates
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/06—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
- C23C14/0641—Nitrides
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/06—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
- C23C14/14—Metallic material, boron or silicon
- C23C14/18—Metallic material, boron or silicon on other inorganic substrates
- C23C14/185—Metallic material, boron or silicon on other inorganic substrates by cathodic sputtering
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/58—After-treatment
- C23C14/5873—Removal of material
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/28—Manufacture of electrodes on semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/268
- H01L21/283—Deposition of conductive or insulating materials for electrodes conducting electric current
- H01L21/285—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation
- H01L21/28506—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers
- H01L21/28512—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers on semiconductor bodies comprising elements of Group IV of the Periodic Table
- H01L21/2855—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers on semiconductor bodies comprising elements of Group IV of the Periodic Table by physical means, e.g. sputtering, evaporation
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76838—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
- H01L21/76841—Barrier, adhesion or liner layers
- H01L21/76843—Barrier, adhesion or liner layers formed in openings in a dielectric
- H01L21/76844—Bottomless liners
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76838—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
- H01L21/76841—Barrier, adhesion or liner layers
- H01L21/76843—Barrier, adhesion or liner layers formed in openings in a dielectric
- H01L21/76846—Layer combinations
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76838—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
- H01L21/76841—Barrier, adhesion or liner layers
- H01L21/76853—Barrier, adhesion or liner layers characterized by particular after-treatment steps
- H01L21/76865—Selective removal of parts of the layer
Definitions
- the present invention is concerned with fabrication of semiconductor devices, and is more particularly concerned with sputtering of materials onto substrates used to fabricate semiconductor devices.
- Semiconductor device fabrication typically involves depositing and patterning a number of layers on a substrate such as a silicon wafer or glass plate.
- a substrate such as a silicon wafer or glass plate.
- One widely used method of forming material layers on substrates is known as sputtering or sputter deposition (also referred to as physical vapor deposition (PVD)).
- PVD physical vapor deposition
- a first conventional PVD reactor is schematically illustrated in cross-section in FIG. 1A .
- the reactor 10 is of a type sometimes referred to as an SIP (self ionizing plasma) chamber.
- Reference numeral 10 generally indicates the PVD reactor.
- the reactor 10 includes a sealable chamber 12 , and a target 14 installed at the top of the chamber 12 .
- the target 14 is composed of a material, usually a metal, to be sputter deposited on a wafer 16 held on a pedestal 18 .
- a shield 20 installed within the chamber 12 protects walls of the chamber 12 from material sputtered from the target 14 and provides a grounding anode.
- a variable (DC) power supply 22 is connected to the target 14 for supplying power thereto.
- a working gas supply 23 which includes a working gas source 24 and a first mass flow controller 26 , supplies a working gas (typically the chemically inactive gas argon) to the chamber 12 .
- a working gas typically the chemically inactive gas argon
- a second gas supply 25 may be provided, including a nitrogen gas source 27 and a second mass flow controller 29 .
- the chamber 12 is shown as receiving argon and nitrogen near the top of the chamber 12 , but may be reconfigured to receive argon and nitrogen at other locations, such as near the bottom of the chamber 12 .
- a pump 28 is provided to pump out the chamber 12 to a pressure at which sputtering is performed; and an RF power source 32 is connected to the pedestal 18 through a coupling capacitor 34 (e.g., for biasing the wafer 16 during sputtering).
- a controller 30 is provided to control operation of the reactor 10 .
- the controller 30 is operatively connected to control the DC power supply 22 , the first mass flow controller 26 , the second mass flow controller 29 , the pump 28 , and the RF power supply 32 .
- the controller 30 similarly may be coupled to control the position and/or temperature of the pedestal 18 .
- the controller 30 may control the distance between the pedestal 18 and the target 14 , as well as heating and/or cooling of the pedestal 18 .
- a magnetron 36 may be rotationally mounted above the target 14 to shape the plasma.
- the magnetron 36 may be of a type which produces an asymmetric magnetic field which extends deep into the chamber 12 (e.g., toward the pedestal 18 ), to enhance the ionization density of the plasma, as disclosed in U.S. Pat. No. 6,183,614.
- U.S. Pat. No. 6,183,614 is hereby incorporated by reference herein in its entirety.
- Typical ionized metal densities may reach 10 10 to 10 11 metal ions/cm 3 when such asymmetric magnetic fields are employed. In such systems, ionized metal atoms follow the magnetic field lines which extend into the chamber 12 , and thus coat the wafer 16 with greater directionality and efficiency.
- the magnetron 36 may rotate, for example, at 60-100 rpm. Stationary magnetic rings may be used instead of the rotating magnetron 36 .
- argon is admitted into the chamber 12 from the working gas supply 23 and the DC power supply 22 is turned on to ignite the argon into a plasma.
- Positive argon ions thereby are generated, and the target 14 is biased negatively relative to the grounded shield 20 .
- These positively charged argon ions are attracted to the negatively biased target 14 , and may strike the target 14 with sufficient energy to cause target atoms to be sputtered from the target 14 .
- Some of the sputtered atoms strike the wafer 16 and are deposited thereon thereby forming a film of the target material on the wafer 16 .
- a DC self bias of the wafer 16 results from operation of the RF power supply 32 , and enhances efficiency of sputter deposition (e.g., by attracting ionized target atoms which strike the wafer 16 with more directionality).
- the use of asymmetric magnetic fields increases ionized metal densities. A larger fraction of sputtered target atoms thereby strike the wafer 16 (with greater directionality).
- sputtering typically is performed at a pressure of about 0-2 milliTorr. Other pressures may be employed.
- the power applied to the target 14 may be, for example, about 18 kW and the RF bias signal applied to the pedestal 18 may be about 250 W or less (although other target powers and RF biases may be used).
- nitrogen is flowed into the chamber 12 from the second gas supply 25 together with argon provided from the working gas supply 23 .
- Nitrogen reacts with the target 14 to form a nitrogen film on the target 14 so that metal nitride is sputtered therefrom. Additionally, non-nitrided atoms are also sputtered from the target 14 . These atoms can combine with nitrogen to form metal nitride in flight or on the wafer 16 .
- FIG. 1B is a schematic cross-sectional view of a second conventional PVD reactor 10 ′.
- the reactor 10 ′ of FIG. 1B may have all of the components described above in connection with the reactor 10 of FIG. 1A .
- the reactor 10 ′ includes a coil 38 which is disposed within the chamber 12 and surrounds a portion of the interior volume of the chamber 12 .
- the coil 38 may comprise a plurality of coils, a single turn coil, a single turn material strip, or any other similar configuration.
- the coil 38 is positioned along the inner surface of the chamber 12 , between the target 14 and the pedestal 18 .
- An RF power source 40 is connected to the coil 38 and is controlled by the controller 30 .
- the RF power source 40 is operated to energize the coil 38 , to enhance the plasma within the chamber 12 (by ionizing target atoms sputtered from the target 14 ).
- the coil 38 typically is energized at about 2 MHz at a power level of 1-3 kW. Other frequencies and/or powers may be used.
- metal ion densities can reach about 10 10 -10 11 metal ions/cm 3 .
- the chamber pressures employed in the reactor 10 ′ of FIG. 1B may be similar to those described above in connection with the reactor 10 of FIG. 1A .
- stationary ring magnets may be used in the reactor 10 ′ of FIG. 1B in place of the rotating magnetron 36 .
- FIG. 1C is a schematic cross-sectional view of a third conventional PVD reactor 10 ′′.
- the reactor 10 ′′ of FIG. 1C may have all the components of the reactor 10 ′ of FIG. 1B , except that in place of the asymmetric magnetron 36 shown in FIG. 1B , a balanced magnetron 42 ( FIG. 1C ) may be provided.
- the magnetic field provided by the balanced magnetron 42 does not extend as far into the chamber 12 as the magnetic field provided by the asymmetric magnetron 36 .
- the reactor 10 ′′ of FIG. 1C is therefore operated at a higher pressure (e.g., 10-100 milliTorr) so that metal atoms sputtered from the target 14 thermalize and have a greater opportunity for ionization.
- a higher pressure e.g., 10-100 milliTorr
- metal atoms sputtered from the target 14 experience more collisions (have a smaller mean free path between collisions) and due to increased collisions have more random motion or a longer transit time within the plasma of the reactor 10 ′′ and thus more opportunity to ionize.
- Metal ion densities within the reactor 10 ′′ may reach about 10 10 -10 11 metal ions/cm 3 , but over a larger volume than in the reactor 10 of FIG. 1A .
- stationary ring magnets may be employed in the reactor 10 ′′ of FIG. 1C .
- FIG. 1D is a schematic cross-sectional view of a fourth conventional PVD reactor 10 ′′′.
- the reactor 10 ′′′ includes a specially shaped target 242 and a magnetron 280 .
- the target 242 or at least its interior surface is composed of the material to be sputter deposited (e.g., copper, titanium, tantalum, tungsten or other materials).
- Reactive sputtering of materials like TiN and TaN can be accomplished by using a Ti or Ta target and including gaseous nitrogen in the plasma. In such a case, the nitrogen is introduced into the reactor 10 ′′′ from a nitrogen gas source which is not shown in FIG. 1D .
- Other combinations of metal targets and reactive gases may be employed.
- the target 242 includes an annularly shaped downwardly facing vault 118 facing a wafer 120 which is to be sputter coated.
- the vault could alternatively be characterized as an annular roof.
- the vault 118 has an aspect ratio of its depth to radial width of at least 1:2 and preferably at least 1:1.
- the vault 118 has an outer sidewall 122 outside of the periphery of the wafer 120 , an inner sidewall 124 overlying the wafer 120 , and a generally flat vault top wall or roof 244 (which closes the bottom of the downwardly facing vault 118 ).
- the target 242 includes a central portion forming a post 126 including the inner sidewall 124 and a generally planar face 128 in parallel opposition to the wafer 120 .
- a cylindrical central well 136 of the target 242 is formed between opposed portions of the inner target sidewall 124 .
- the target 242 also includes a flange 129 that is vacuum sealed to a grounded chamber body 150 of the reactor 10 ′′′ through a dielectric target isolator 152 .
- the wafer 120 is clamped to a heater pedestal electrode 154 by, for example, a clamp ring 156 although electrostatic chucking may alternatively be employed.
- An electrically grounded shield 158 acts as an anode with respect to the cathode target 242 , which is negatively energized by a power supply 160 .
- RF sputtering can also be employed, and may be particularly useful for sputtering non-metallic targets.
- An electrically floating shield 162 is supported on the electrically grounded shield 158 or chamber 150 by a dielectric shield isolator 164 .
- a cylindrical knob 166 extending downwardly from the outer target sidewall 122 and positioned inwardly of the uppermost part of the floating shield 162 protects the upper portion of the floating shield 162 and the target isolator 152 from sputter deposition from the strong plasma disposed within the target vault 118 .
- the gap between the upper portion of the floating shield 162 and the target knob 166 and the flange 129 is small enough to act as a dark space (preventing a plasma from propagating into the gap).
- a working gas such as argon is supplied into the reactor 10 ′′′ from a gas source 168 through a mass flow controller 170 .
- a vacuum pumping system 172 maintains the chamber at a reduced pressure, typically a base pressure of about 10 ⁇ 8 Torr.
- An RF power supply 174 RF biases the pedestal electrode 154 through an isolation capacitor (not shown), to produce a negative DC self-bias. Alternatively, the RF power supply may be omitted and the pedestal electrode 154 may be allowed to float to develop a negative self-bias.
- a controller 176 regulates the power supplies 160 , 174 , mass flow controller 170 , and vacuum system 172 (e.g., according to a sputtering recipe stored in the controller 176 ). The controller 176 also may control the position and/or temperature of the pedestal electrode 154 .
- the magnetron 280 includes inner and outer top magnets 272 , 274 overlying the vault roof 244 .
- Side magnets 282 , 284 disposed outside of the vault sidewalls 122 , 124 have opposed vertical magnetic polarities but are largely decoupled from the top magnets 272 , 274 because they are supported on a magnetic yoke 188 by non-magnetic supports 286 , 288 .
- the side magnets 282 , 284 create a magnetic field B in the vault 118 that has two generally anti-parallel components extending radially across the vault 118 as well as two components extending generally parallel to the trough sidewalls.
- the magnetic field B extends over a substantial depth of the vault 118 and repels electrons from the sidewalls 122 , 124 .
- a magnetic field B′ is formed by top magnets 272 , 274 .
- a motor 190 is supported on the chamber body 150 by means of a cylindrical sidewall 192 and a roof 194 , which are preferably electrically isolated from the biased target flange 129 .
- the motor 190 has a motor shaft connected to the yoke 188 at a central axis 116 of the target 242 .
- the motor 190 may rotate the magnetron 280 about the axis 116 at a suitable rate (e.g., about 50 rpm or greater).
- the yoke 188 is asymmetric and may be shaped as a sector. Mechanical counterbalancing may be provided to reduce vibration in the rotation of the axially offset magnetron 280 .
- magnets of the magnetron 280 may be replaced by stationary ring magnets.
- the pressure level employed during sputtering in the reactor 10 ′′′ of FIG. 1D may be similar to the pressure level employed during sputtering in the reactor 10 of FIG. 1A .
- the reactor 10 ′′′ of FIG. 1D produces ionized metal densities in the range of 10 10 -10 11 metal ions/cm 3 without requiring a coil and over a larger volume than in the reactor 10 of FIG. 1A .
- Target power may be in the range of about 20-40 kW although other power ranges may be employed.
- a reactor of the type shown in FIG. 1D is disclosed in U.S. Pat. No. 6,277,249, which is hereby incorporated by reference herein in its entirety.
- U.S. Pat. No. 6,251,242 is related to U.S. Pat. No. 6,277,249 and is also incorporated by reference herein in its entirety.
- the multi-layer structure of typical semiconductor devices requires that connections be made between layers of the devices.
- holes or other features are formed in dielectric layers that isolate adjacent conductive layers from each other, and the holes are filled with conductive material (e.g., metal).
- conductive material e.g., metal
- a connecting hole is referred to as a “contact”; if the lower layer is a metallization layer then the connecting hole is referred to as a “via”.
- the term “via” should be understood to include both contact holes and via holes, as well as other similar features such as lines and/or trenches.
- barrier layer is to prevent diffusion of the copper into the dielectric layer through which the via or other feature is formed.
- FIG. 2 is a schematic cross-sectional view of a dual damascene structure 300 which has been coated with a barrier layer 302 in accordance with conventional practice. It should be understood that FIG. 2 is not drawn to scale and is merely representative.
- the dual damascene structure 300 has been formed in a dielectric layer 304 , and includes a trench 306 and vias 308 .
- the vias 308 have bottoms 310 and side walls 312 .
- the barrier layer 302 may be formed by sputter-depositing a tantalum nitride layer 314 , followed by sputter-depositing a tantalum layer 316 .
- the tantalum nitride layer 314 generally is deposited so as to have a thickness of about 100 angstroms at a field region 318 of the substrate.
- the tantalum layer 316 generally is deposited so as to have a thickness of about 150 angstroms at the field region 318 .
- a problem which is encountered with the conventional barrier layer 302 of FIG. 2 is asymmetry in the barrier layer, particularly at the lower portion of the via side wall 312 (near bottom 310 ), as indicated by reference numeral 320 . Such asymmetry may result in inadequate side wall coverage and less than desirable performance of the barrier layer 302 .
- a first method for forming a barrier layer on a substrate.
- the first method includes the step of sputter-depositing a tantalum nitride layer on a substrate having (1) a metal feature formed on the substrate; (2) a dielectric layer formed over the metal feature; and (3) a via formed in the dielectric layer so as to expose the metal feature.
- the via has side walls and a bottom, and a width of about 0.18 microns or less.
- the tantalum nitride layer is deposited on the side walls and bottom of the via and on a field region of the dielectric layer; and has a thickness of at least about 200 angstroms on the field region of the dielectric layer upon completion of the sputter-depositing of the tantalum nitride layer.
- the first method also includes the step of sputter-depositing a tantalum layer on the substrate, in the same chamber used to sputter deposit the tantalum nitride layer.
- the tantalum layer having a thickness of less than about 100 angstroms on the field region of the dielectric layer upon completion of the sputter-depositing of the tantalum layer.
- a second inventive method for forming a barrier layer on a substrate.
- the second inventive method is similar to the first inventive method, but includes the step of back sputtering at least a portion of the tantalum nitride layer from the bottom of the via of the substrate prior to the step of sputter-depositing the tantalum layer.
- inventive methods and apparatus provided herein reflect a recognition on the part of the present inventors that the problem of side wall asymmetry in a conventional barrier layer formed from a tantalum nitride layer and a tantalum layer is largely due to asymmetry in the tantalum layer. Consequently, in one or more aspects of the present invention, the thickness of the tantalum layer is reduced, while increasing the thickness of the tantalum nitride layer.
- Prior art practices have called for a tantalum nitride layer having a thickness of about 100 angstroms and a tantalum layer having a thickness of at least 100 angstroms on the field region of a substrate.
- aspects the invention provide for a tantalum nitride layer of about 200 angstroms or greater and a tantalum layer of less than about 100 angstroms on the field region of the substrate.
- the thickness of the tantalum layer is about 30-50 angstroms on the field region of the substrate. Numerous other aspects are provided.
- FIG. 1A is a schematic cross-sectional view of a first conventional plasma sputtering reactor
- FIG. 1B is a schematic cross-sectional view of a second conventional plasma sputtering reactor
- FIG. 1C is a schematic cross-sectional view of a third conventional plasma sputtering reactor
- FIG. 1D is a schematic cross-sectional view of a fourth conventional plasma sputtering reactor
- FIG. 2 is a schematic cross-sectional view of a dual damascene structure that has been coated with a barrier layer in accordance with a conventional process
- FIG. 3 is a flow chart that illustrates a method of forming a barrier layer on a substrate in accordance with the present invention
- FIGS. 4A-4C are schematic cross-sectional views of a dual damascene structure at various stages of the inventive process of FIG. 3 ;
- FIG. 4D is a view similar to FIGS. 4A-4C showing the dual damascene structure after copper-filling subsequent to the process of FIG. 3 ;
- FIGS. 5A-5D are schematic cross-sectional views of a dual damascene structure at various stages of an alternate inventive barrier layer process.
- a barrier layer is formed in a via that has been formed in a dielectric layer on a substrate.
- the barrier layer may be formed, for example, employing a three-step process.
- a tantalum nitride layer is sputter-deposited on a bottom, side walls and field region of the via.
- the tantalum nitride layer is back sputtered from the bottom of the via to reduce or eliminate the bottom tantalum nitride layer, and to improve side wall coverage.
- a brief or “flash” sputter-deposition of tantalum is performed to provide suitable wetting for subsequent copper seed layer deposition.
- FIG. 3 is a flow chart that illustrates an exemplary process performed in accordance with the present invention.
- the process of FIG. 3 may be performed, for example, in a sputtering reactor of the type illustrated in FIG. 1B .
- the process of FIG. 3 begins with a step 330 , at which a tantalum nitride layer is sputter-deposited by a reactive sputtering process. That is, referring to FIG. 1B , the target 14 (a tantalum target) is energized by means of the DC power supply 22 . Argon is flowed to the chamber 12 via the mass flow controller 26 , and nitrogen is flowed to the chamber 12 via the mass flow controller 29 .
- the chamber pressure may be about 10 mTorr or less, and more preferably in the range of about 2-4 mTorr. Other pressures may be employed.
- the power signal supplied to the target 14 by the DC power supply 22 may be about 20 kW (or less), and a bias signal in the range 0-150 W may be supplied to the pedestal 18 by the RF power supply 32 .
- the target power may be about 40 kW (or less) and the bias power may be in the range of about 0-300 W. Other power ranges may be employed.
- the coil 38 is not energized during step 330 .
- step 330 may have a duration in the range of about 7-10 seconds (although other durations may be employed).
- FIG. 4A is a schematic cross-sectional view showing a dual damascene structure 300 ′ upon completion of step 330 .
- Reference numeral 400 indicates a tantalum nitride layer deposited during step 330 .
- FIG. 4A shows the same dielectric layer 304 , trench 306 , vias 308 , via bottoms 310 , via side walls 312 and field region 318 as were referred to in connection with FIG. 2 . Like FIG. 2 (and also FIGS. 4B-4D ), FIG. 4A is not drawn to scale.
- the tantalum nitride layer 400 may have a thickness on the field region 318 of greater than about 200 angstroms, and preferably about 220 angstroms. Thicknesses in the range of about 100-400 angstroms may also be employed.
- step 330 is followed by step 332 .
- the tantalum layer 400 is at least partially back sputtered from the via bottoms 310 .
- substantially all of the tantalum nitride layer 400 is back sputtered from the via bottoms 310 .
- argon is flowed to the chamber 12 via the mass flow controller 26 , but nitrogen is not flowed to the chamber 12 .
- the pressure in the chamber 12 may be, for example, less than about 10 mTorr and more preferably in the range of about 1-3 mTorr.
- a bias signal is supplied to the pedestal 18 by the RF power supply 32 .
- the bias signal may be, for example, in the range of about 200-500 W, and in one embodiment may be about 300 W. If the reactor 10 ′ is adapted to process 300 millimeter substrates, the bias signal may be, for example, in the range of about 400-1000 W.
- the coil 38 may be energized by the RF power source 40 (e.g., at about 2 MHz), for example, at a power level in the range of about 1000-3000 W.
- the target 14 may be energized with a power level in the range of about 0-1000 W.
- a plasma which is ignited in the chamber 12 causes back sputtering of the tantalum nitride layer 400 from the via bottom walls 310 .
- the duration of the back sputtering step 332 may be in the range of about 5-15 seconds.
- Other chamber pressures, pedestal biases, coil powers, target powers and/or back sputter durations may be employed.
- FIG. 4B is a view similar to FIG. 4A , showing the condition of the dual damascene structure 300 ′ upon completion of step 332 .
- the via bottoms 310 may be substantially free of the tantalum nitride layer 400 upon completion of step 332 .
- coverage/uniformity of the via side walls 312 with tantalum nitride may be improved.
- the thickness of the tantalum nitride layer 400 at the field region 318 may be reduced from about 220 angstroms to about 200 angstroms upon completion of step 332 .
- the back sputtering step may (1) substantially eliminate the tantalum nitride layer on the bottoms 310 of the vias 308 (thereby improving the contact resistance of any interconnect formed therein); (2) increase the thickness and/or uniformity of the tantalum nitride layer on the side walls 312 of the vias 308 (thereby improving the diffusion resistance of the tantalum nitride barrier layer); and/or (3) only slightly thin the tantalum nitride layer on the field region 318 (thereby maintaining adequate diffusion resistance for the dielectric layer 304 ).
- step 334 follows step 332 .
- a brief (so-called “flash”) sputter-deposition of a tantalum layer is performed.
- argon is flowed to the chamber 12 via the mass flow controller 26 , but nitrogen is not flowed to the chamber 12 .
- the pressure in the chamber 12 during step 334 may be, for example, less than about 10 mTorr and more preferably in the range of about 1-3 mTorr.
- the coil 38 need not be energized during step 334 , and the target and bias power levels may be similar to those described in connection with step 330 .
- the duration of step 334 may be less than about two seconds, and, in one embodiment, may be in the range of about 1-1.5 seconds.
- the target 14 is energized and a plasma is ignited in the chamber 12 to perform sputter-deposition of a tantalum layer on the dual damascene structure 300 ′.
- Other chamber pressures, pedestal biases, coil powers, target powers and/or durations may be employed.
- FIG. 4C illustrates the dual damascene structure 300 ′ upon completion of step 334 .
- Reference numeral 402 indicates the tantalum layer deposited during step 334 .
- the tantalum layer 402 may have, upon completion of step 334 , a thickness in the range of about 30-50 angstroms on the field region 318 .
- the thickness of the tantalum layer 402 on the via bottom walls 310 may be in the range of about 20-40 angstroms.
- the side-wall coverage may be about 10 angstroms. Other thicknesses may be employed.
- the target power during step 334 may be less than indicated above (e.g., the target power may be about 5 kW or less) in which case the step 334 may have a longer duration.
- controller 30 may be programmed to perform one or more of the steps of the process of FIG. 3 within the reactor 10 ′.
- FIG. 1B While the present invention has been described as applied in a plasma sputtering reactor of the type illustrated in FIG. 1B , it will be understood that the present invention may be applied in other types of plasma sputtering reactors, including those illustrated in FIGS. 1A, 1C and 1 D. However, the reactor of FIG. 1B is believed to be particularly advantageous in view of the back sputtering efficiency promoted by energizing the coil 38 .
- FIG. 4D is a view similar to FIG. 4A , showing the dual damascene structure 300 ′ upon completion of copper fill and planarization processes that may be performed after the process of FIG. 3 .
- the filling of the dual damascene structure 300 ′ with copper may include sputter-deposition of a copper seed layer on the substrate 403 (e.g., in a different reactor than that employed for tantalum nitride and tantalum deposition), followed by copper electrochemical deposition (e.g., electrochemical plating).
- reference numeral 404 indicates the copper fill of the dual damascene structure 300 ′ after formation of a barrier layer that includes the tantalum nitride layer 400 and the tantalum layer 402 .
- the present invention also may provide a fourth step for the process of FIG. 3 , in which back sputtering is performed with respect to the tantalum layer 402 (e.g., to further reduce interconnect resistance).
- back sputtering is performed with respect to the tantalum layer 402 (e.g., to further reduce interconnect resistance).
- the thicknesses of the tantalum nitride layer 400 and the tantalum layer 402 on the field region 318 as described may be suitable in conjunction with a 0.13 micron generation of semiconductor devices, in which a typical via width may be about 0.18 microns, and a typical aspect ratio of a via may be in the range of about 4:1 to 6:1.
- the thickness of the tantalum nitride layer on the field region may be in the range of about 100-400 angstroms, and the thickness of the tantalum layer on the field region may be any thickness less than about 100 angstroms. It is also contemplated to employ the tantalum nitride and tantalum layer thicknesses according to the present invention in connection with via widths that are less than 0.18 microns.
- inventive methods and apparatus disclosed herein provide for satisfactory barrier layer side wall coverage with reduced asymmetry, together with suitable wetting for subsequent deposition of a copper seed layer.
- one or more of the steps of the process of FIG. 3 may be implemented in computer program code as one or more computer program products.
- Each inventive computer program product may be carried by a medium readable by a computer (e.g., a carrier wave signal, a floppy disk, a hard drive, a random access memory, etc.).
- Such computer program code and/or computer program products may be executed, for example, by one or more of the controllers 30 , 176 of FIGS. 1A-1D .
- a step of sputter-depositing an initial tantalum layer (e.g., with a field region thickness of 100 angstroms or more) is performed after step 330 and before step 332 .
- substantially all of the resulting tantalum and tantalum nitride layers may be removed from the via bottoms. Step 334 is then performed as described above.
- FIGS. 5A-5D are cross-sectional views of a dual damascene structure 300 ′′ at various stages of such an alternate process. For clarity purposes, no asymmetry in layer thickness is shown in FIGS. 5A-5D .
- a tantalum nitride layer 500 is deposited on the bottoms 310 and side walls 312 of the vias 308 (Step 330 , FIG. 3 ).
- An initial tantalum layer 501 ( FIG. 5B ) then is deposited over the tantalum nitride layer 500 (step not shown in FIG. 3 ). Thereafter, both the tantalum layer 501 and the tantalum nitride layer 500 are back sputtered from the bottoms 310 of the vias 308 (thereby improving barrier layer coverage on the side walls 312 ), as shown in FIG. 5C (and/or Step 332 of FIG. 3 ).
- a thin tantalum flash layer 502 then may be formed over the bottom and/or side walls of the vias 308 ( FIG. 5D and/or Step 334 in FIG. 3 ).
- the dual damascene structure 300 ′′ then may be filled and/or planarized as previously described (e.g., via use of a copper seed layer and/or electrochemical deposition).
- the tantalum nitride layer 500 may have a thickness of about 50-100 angstroms on the field region 318 of the dielectric layer 304 , a thickness of about 10-20 angstroms on the side walls 312 of the vias 308 and a thickness of about 10-70 angstroms on the bottoms 310 of the vias 308 .
- the initial tantalum layer 501 may have a thickness of about 100-300 angstroms on the field region 318 of the dielectric layer 304 , a thickness of about 20-40 angstroms on the side walls 312 of the vias 308 and a thickness of about 30-180 angstroms on the bottoms 310 of the vias 308 .
- the total barrier layer thickness on the side walls 312 may be about 50 ⁇ or more (and may include a tantalum nitride/tantalum/tantalum nitride stack).
- the tantalum flash layer 502 may add a thickness of about 50-100 angstroms (of tantalum) on the field region 318 , a thickness of about 5-15 angstroms on the side walls 312 and a thickness of about 15-50 angstroms on the bottoms 310 .
- the tantalum flash layer 502 is optional, and if employed, may result in side walls 312 having barrier layers of tantalum nitride/tantalum/tantalum nitride/tantalum. Other thicknesses may be employed for the tantalum and tantalum nitride layers.
- the tantalum nitride and/or tantalum layers in accordance with the present invention it may be preferable to maintain a significant neutral metal density (e.g., by sputtering target atoms during back sputtering) and ion density (e.g., by applying power to an RF coil or by employing any other known means for increasing ion density) during back sputtering. Maintaining a significant neutral metal density during back sputtering may reduce and/or prevent over etching of bevel regions 506 ( FIGS.
- a high density plasma physical vapor deposition (HDPPVD) chamber may include any PVD chamber capable of sustaining a plasma having an ion density of at least 10 10 ions/cm 3 in a bulk region of the plasma (e.g., a region, between a target/cathode and substrate support pedestal, that is not immediately adjacent the target/cathode; although an area immediately adjacent the target/cathode also may have an ion density of at least 10 10 ions/cm 3 ).
- a bulk region of the plasma e.g., a region, between a target/cathode and substrate support pedestal, that is not immediately adjacent the target/cathode; although an area immediately adjacent the target/cathode also may have an ion density of at least 10 10 ions/cm 3 ).
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Abstract
A first method is provided for forming a barrier layer on a substrate by sputter-depositing a tantalum nitride layer on a substrate having (1) a metal feature formed on the substrate; (2) a dielectric layer formed over the metal feature; and (3) a via formed in the dielectric layer so as to expose the metal feature. The via has side walls and a bottom, and a width of about 0.18 microns or less. The tantalum nitride layer is deposited on the side walls and bottom of the via and on a field region of the dielectric layer; and has a thickness of at least about 200 angstroms on the field region. The first method also includes sputter-depositing a tantalum layer on the substrate, in the same chamber. The tantalum layer having a thickness of less than about 100 angstroms on the field region. Other aspects are provided.
Description
- This application is a division of and claims priority from U.S. patent application Ser. No. 10/409,406 filed Apr. 7, 2003, which claims priority from U.S. Provisional Patent Application Ser. No. 60/430,267, filed Dec. 2, 2002 and titled “Method and Apparatus for Sputter Deposition”. Each of these applications is hereby incorporated by reference herein in its entirety.
- The present application is related to U.S. Provisional Patent Application Ser. Nos. 60/380,385 and 60/380,386, both filed on May 14, 2002 and titled “Method and Apparatus for Sputter Deposition” (Attorney Docket Nos. 6221 and 6172). These provisional applications are hereby incorporated by reference herein in their entirety.
- The present invention is concerned with fabrication of semiconductor devices, and is more particularly concerned with sputtering of materials onto substrates used to fabricate semiconductor devices.
- Semiconductor device fabrication typically involves depositing and patterning a number of layers on a substrate such as a silicon wafer or glass plate. One widely used method of forming material layers on substrates is known as sputtering or sputter deposition (also referred to as physical vapor deposition (PVD)).
- A first conventional PVD reactor is schematically illustrated in cross-section in
FIG. 1A . Thereactor 10 is of a type sometimes referred to as an SIP (self ionizing plasma) chamber.Reference numeral 10 generally indicates the PVD reactor. Thereactor 10 includes asealable chamber 12, and atarget 14 installed at the top of thechamber 12. Thetarget 14 is composed of a material, usually a metal, to be sputter deposited on awafer 16 held on apedestal 18. Ashield 20 installed within thechamber 12 protects walls of thechamber 12 from material sputtered from thetarget 14 and provides a grounding anode. A variable (DC)power supply 22 is connected to thetarget 14 for supplying power thereto. - A working
gas supply 23, which includes a workinggas source 24 and a firstmass flow controller 26, supplies a working gas (typically the chemically inactive gas argon) to thechamber 12. If reactive sputtering is to be performed to sputter-deposit a metal nitride layer, such as TaN, asecond gas supply 25 may be provided, including anitrogen gas source 27 and a secondmass flow controller 29. Thechamber 12 is shown as receiving argon and nitrogen near the top of thechamber 12, but may be reconfigured to receive argon and nitrogen at other locations, such as near the bottom of thechamber 12. Apump 28 is provided to pump out thechamber 12 to a pressure at which sputtering is performed; and anRF power source 32 is connected to thepedestal 18 through a coupling capacitor 34 (e.g., for biasing thewafer 16 during sputtering). - A
controller 30 is provided to control operation of thereactor 10. Thecontroller 30 is operatively connected to control theDC power supply 22, the firstmass flow controller 26, the secondmass flow controller 29, thepump 28, and theRF power supply 32. Thecontroller 30 similarly may be coupled to control the position and/or temperature of thepedestal 18. For example, thecontroller 30 may control the distance between thepedestal 18 and thetarget 14, as well as heating and/or cooling of thepedestal 18. To promote efficient sputtering, amagnetron 36 may be rotationally mounted above thetarget 14 to shape the plasma. Themagnetron 36 may be of a type which produces an asymmetric magnetic field which extends deep into the chamber 12 (e.g., toward the pedestal 18), to enhance the ionization density of the plasma, as disclosed in U.S. Pat. No. 6,183,614. U.S. Pat. No. 6,183,614 is hereby incorporated by reference herein in its entirety. Typical ionized metal densities may reach 1010 to 1011 metal ions/cm3 when such asymmetric magnetic fields are employed. In such systems, ionized metal atoms follow the magnetic field lines which extend into thechamber 12, and thus coat thewafer 16 with greater directionality and efficiency. Themagnetron 36 may rotate, for example, at 60-100 rpm. Stationary magnetic rings may be used instead of the rotatingmagnetron 36. - In operation, argon is admitted into the
chamber 12 from the workinggas supply 23 and theDC power supply 22 is turned on to ignite the argon into a plasma. Positive argon ions thereby are generated, and thetarget 14 is biased negatively relative to thegrounded shield 20. These positively charged argon ions are attracted to the negativelybiased target 14, and may strike thetarget 14 with sufficient energy to cause target atoms to be sputtered from thetarget 14. Some of the sputtered atoms strike thewafer 16 and are deposited thereon thereby forming a film of the target material on thewafer 16. - A DC self bias of the
wafer 16 results from operation of theRF power supply 32, and enhances efficiency of sputter deposition (e.g., by attracting ionized target atoms which strike thewafer 16 with more directionality). As stated, the use of asymmetric magnetic fields increases ionized metal densities. A larger fraction of sputtered target atoms thereby strike the wafer 16 (with greater directionality). - Within the
reactor 10, sputtering typically is performed at a pressure of about 0-2 milliTorr. Other pressures may be employed. The power applied to thetarget 14 may be, for example, about 18 kW and the RF bias signal applied to thepedestal 18 may be about 250 W or less (although other target powers and RF biases may be used). - If reactive sputtering is to be performed, nitrogen is flowed into the
chamber 12 from thesecond gas supply 25 together with argon provided from the workinggas supply 23. Nitrogen reacts with thetarget 14 to form a nitrogen film on thetarget 14 so that metal nitride is sputtered therefrom. Additionally, non-nitrided atoms are also sputtered from thetarget 14. These atoms can combine with nitrogen to form metal nitride in flight or on thewafer 16. -
FIG. 1B is a schematic cross-sectional view of a secondconventional PVD reactor 10′. Thereactor 10′ ofFIG. 1B may have all of the components described above in connection with thereactor 10 ofFIG. 1A . In addition thereactor 10′ includes acoil 38 which is disposed within thechamber 12 and surrounds a portion of the interior volume of thechamber 12. Thecoil 38 may comprise a plurality of coils, a single turn coil, a single turn material strip, or any other similar configuration. Thecoil 38 is positioned along the inner surface of thechamber 12, between thetarget 14 and thepedestal 18. - An
RF power source 40 is connected to thecoil 38 and is controlled by thecontroller 30. During sputter-deposition operation of thereactor 10′, theRF power source 40 is operated to energize thecoil 38, to enhance the plasma within the chamber 12 (by ionizing target atoms sputtered from the target 14). Thecoil 38 typically is energized at about 2 MHz at a power level of 1-3 kW. Other frequencies and/or powers may be used. As with thereactor 10 ofFIG. 1A , metal ion densities can reach about 1010-1011 metal ions/cm3. However, because of the energy provided by thecoil 38, high metal ion densities may be provided over a wider region of the plasma of thereactor 10 than for the plasma of thereactor 10 ofFIG. 1A . The chamber pressures employed in thereactor 10′ ofFIG. 1B may be similar to those described above in connection with thereactor 10 ofFIG. 1A . As was the case with thereactor 10 ofFIG. 1A , stationary ring magnets may be used in thereactor 10′ ofFIG. 1B in place of the rotatingmagnetron 36. -
FIG. 1C is a schematic cross-sectional view of a thirdconventional PVD reactor 10″. Thereactor 10″ ofFIG. 1C may have all the components of thereactor 10′ ofFIG. 1B , except that in place of theasymmetric magnetron 36 shown inFIG. 1B , a balanced magnetron 42 (FIG. 1C ) may be provided. The magnetic field provided by thebalanced magnetron 42 does not extend as far into thechamber 12 as the magnetic field provided by theasymmetric magnetron 36. Thereactor 10″ ofFIG. 1C is therefore operated at a higher pressure (e.g., 10-100 milliTorr) so that metal atoms sputtered from thetarget 14 thermalize and have a greater opportunity for ionization. That is, at the higher pressure at which thereactor 10″ operates, metal atoms sputtered from thetarget 14 experience more collisions (have a smaller mean free path between collisions) and due to increased collisions have more random motion or a longer transit time within the plasma of thereactor 10″ and thus more opportunity to ionize. Metal ion densities within thereactor 10″ may reach about 1010-1011 metal ions/cm3, but over a larger volume than in thereactor 10 ofFIG. 1A . - As in the case of the
reactors reactor 10″ ofFIG. 1C . -
FIG. 1D is a schematic cross-sectional view of a fourthconventional PVD reactor 10′″. Thereactor 10′″ includes a specially shapedtarget 242 and amagnetron 280. Thetarget 242 or at least its interior surface is composed of the material to be sputter deposited (e.g., copper, titanium, tantalum, tungsten or other materials). Reactive sputtering of materials like TiN and TaN can be accomplished by using a Ti or Ta target and including gaseous nitrogen in the plasma. In such a case, the nitrogen is introduced into thereactor 10′″ from a nitrogen gas source which is not shown inFIG. 1D . Other combinations of metal targets and reactive gases may be employed. - The
target 242 includes an annularly shaped downwardly facingvault 118 facing awafer 120 which is to be sputter coated. The vault could alternatively be characterized as an annular roof. Thevault 118 has an aspect ratio of its depth to radial width of at least 1:2 and preferably at least 1:1. Thevault 118 has anouter sidewall 122 outside of the periphery of thewafer 120, aninner sidewall 124 overlying thewafer 120, and a generally flat vault top wall or roof 244 (which closes the bottom of the downwardly facing vault 118). Thetarget 242 includes a central portion forming apost 126 including theinner sidewall 124 and a generallyplanar face 128 in parallel opposition to thewafer 120. A cylindrical central well 136 of thetarget 242 is formed between opposed portions of theinner target sidewall 124. Thetarget 242 also includes aflange 129 that is vacuum sealed to a groundedchamber body 150 of thereactor 10′″ through adielectric target isolator 152. - The
wafer 120 is clamped to aheater pedestal electrode 154 by, for example, aclamp ring 156 although electrostatic chucking may alternatively be employed. An electrically groundedshield 158 acts as an anode with respect to thecathode target 242, which is negatively energized by apower supply 160. As an alternative to DC sputtering, RF sputtering can also be employed, and may be particularly useful for sputtering non-metallic targets. - An electrically floating
shield 162 is supported on the electrically groundedshield 158 orchamber 150 by adielectric shield isolator 164. Acylindrical knob 166 extending downwardly from theouter target sidewall 122 and positioned inwardly of the uppermost part of the floatingshield 162 protects the upper portion of the floatingshield 162 and thetarget isolator 152 from sputter deposition from the strong plasma disposed within thetarget vault 118. The gap between the upper portion of the floatingshield 162 and thetarget knob 166 and theflange 129 is small enough to act as a dark space (preventing a plasma from propagating into the gap). - A working gas such as argon is supplied into the
reactor 10′″ from agas source 168 through amass flow controller 170. Avacuum pumping system 172 maintains the chamber at a reduced pressure, typically a base pressure of about 10−8 Torr. AnRF power supply 174 RF biases thepedestal electrode 154 through an isolation capacitor (not shown), to produce a negative DC self-bias. Alternatively, the RF power supply may be omitted and thepedestal electrode 154 may be allowed to float to develop a negative self-bias. Acontroller 176 regulates the power supplies 160, 174,mass flow controller 170, and vacuum system 172 (e.g., according to a sputtering recipe stored in the controller 176). Thecontroller 176 also may control the position and/or temperature of thepedestal electrode 154. - The
magnetron 280 includes inner and outertop magnets vault roof 244.Side magnets top magnets magnetic yoke 188 bynon-magnetic supports side magnets vault 118 that has two generally anti-parallel components extending radially across thevault 118 as well as two components extending generally parallel to the trough sidewalls. Thus the magnetic field B extends over a substantial depth of thevault 118 and repels electrons from thesidewalls top magnets - A
motor 190 is supported on thechamber body 150 by means of acylindrical sidewall 192 and aroof 194, which are preferably electrically isolated from thebiased target flange 129. Themotor 190 has a motor shaft connected to theyoke 188 at acentral axis 116 of thetarget 242. Themotor 190 may rotate themagnetron 280 about theaxis 116 at a suitable rate (e.g., about 50 rpm or greater). Theyoke 188 is asymmetric and may be shaped as a sector. Mechanical counterbalancing may be provided to reduce vibration in the rotation of the axially offsetmagnetron 280. - Some or all of the magnets of the
magnetron 280 may be replaced by stationary ring magnets. - The pressure level employed during sputtering in the
reactor 10′″ ofFIG. 1D may be similar to the pressure level employed during sputtering in thereactor 10 ofFIG. 1A . Thereactor 10′″ ofFIG. 1D produces ionized metal densities in the range of 1010-1011 metal ions/cm3 without requiring a coil and over a larger volume than in thereactor 10 ofFIG. 1A . Target power may be in the range of about 20-40 kW although other power ranges may be employed. - A reactor of the type shown in
FIG. 1D is disclosed in U.S. Pat. No. 6,277,249, which is hereby incorporated by reference herein in its entirety. U.S. Pat. No. 6,251,242 is related to U.S. Pat. No. 6,277,249 and is also incorporated by reference herein in its entirety. - The multi-layer structure of typical semiconductor devices requires that connections be made between layers of the devices. For this purpose, holes or other features are formed in dielectric layers that isolate adjacent conductive layers from each other, and the holes are filled with conductive material (e.g., metal). If a lower layer to which a connection is made is the semiconductor substrate, then a connecting hole is referred to as a “contact”; if the lower layer is a metallization layer then the connecting hole is referred to as a “via”. As used herein, the term “via” should be understood to include both contact holes and via holes, as well as other similar features such as lines and/or trenches.
- With the use of copper for metallization layers in semiconductor devices, it has become conventional to coat vias with barrier layers before filling with copper. The purpose of the barrier layer is to prevent diffusion of the copper into the dielectric layer through which the via or other feature is formed.
-
FIG. 2 is a schematic cross-sectional view of adual damascene structure 300 which has been coated with abarrier layer 302 in accordance with conventional practice. It should be understood thatFIG. 2 is not drawn to scale and is merely representative. Thedual damascene structure 300 has been formed in adielectric layer 304, and includes atrench 306 andvias 308. Thevias 308 havebottoms 310 andside walls 312. - In accordance with conventional practice, the
barrier layer 302 may be formed by sputter-depositing atantalum nitride layer 314, followed by sputter-depositing atantalum layer 316. According to this conventional practice, thetantalum nitride layer 314 generally is deposited so as to have a thickness of about 100 angstroms at afield region 318 of the substrate. Thetantalum layer 316 generally is deposited so as to have a thickness of about 150 angstroms at thefield region 318. - A problem which is encountered with the
conventional barrier layer 302 ofFIG. 2 is asymmetry in the barrier layer, particularly at the lower portion of the via side wall 312 (near bottom 310), as indicated byreference numeral 320. Such asymmetry may result in inadequate side wall coverage and less than desirable performance of thebarrier layer 302. - In a first aspect of the invention, a first method is provided for forming a barrier layer on a substrate. The first method includes the step of sputter-depositing a tantalum nitride layer on a substrate having (1) a metal feature formed on the substrate; (2) a dielectric layer formed over the metal feature; and (3) a via formed in the dielectric layer so as to expose the metal feature. The via has side walls and a bottom, and a width of about 0.18 microns or less. The tantalum nitride layer is deposited on the side walls and bottom of the via and on a field region of the dielectric layer; and has a thickness of at least about 200 angstroms on the field region of the dielectric layer upon completion of the sputter-depositing of the tantalum nitride layer.
- The first method also includes the step of sputter-depositing a tantalum layer on the substrate, in the same chamber used to sputter deposit the tantalum nitride layer. The tantalum layer having a thickness of less than about 100 angstroms on the field region of the dielectric layer upon completion of the sputter-depositing of the tantalum layer.
- In a second aspect of the invention, a second inventive method is provided for forming a barrier layer on a substrate. The second inventive method is similar to the first inventive method, but includes the step of back sputtering at least a portion of the tantalum nitride layer from the bottom of the via of the substrate prior to the step of sputter-depositing the tantalum layer. Numerous other aspects are provided, as are systems and apparatus in accordance with these and other aspects of the invention.
- The inventive methods and apparatus provided herein reflect a recognition on the part of the present inventors that the problem of side wall asymmetry in a conventional barrier layer formed from a tantalum nitride layer and a tantalum layer is largely due to asymmetry in the tantalum layer. Consequently, in one or more aspects of the present invention, the thickness of the tantalum layer is reduced, while increasing the thickness of the tantalum nitride layer. Prior art practices have called for a tantalum nitride layer having a thickness of about 100 angstroms and a tantalum layer having a thickness of at least 100 angstroms on the field region of a substrate. By contrast, aspects the invention provide for a tantalum nitride layer of about 200 angstroms or greater and a tantalum layer of less than about 100 angstroms on the field region of the substrate. In at least one embodiment of the invention, the thickness of the tantalum layer is about 30-50 angstroms on the field region of the substrate. Numerous other aspects are provided.
- Other features and aspects of the present invention will become more fully apparent from the following detailed description, the appended claims and the accompanying drawings.
-
FIG. 1A is a schematic cross-sectional view of a first conventional plasma sputtering reactor; -
FIG. 1B is a schematic cross-sectional view of a second conventional plasma sputtering reactor; -
FIG. 1C is a schematic cross-sectional view of a third conventional plasma sputtering reactor; -
FIG. 1D is a schematic cross-sectional view of a fourth conventional plasma sputtering reactor; -
FIG. 2 is a schematic cross-sectional view of a dual damascene structure that has been coated with a barrier layer in accordance with a conventional process; -
FIG. 3 is a flow chart that illustrates a method of forming a barrier layer on a substrate in accordance with the present invention; -
FIGS. 4A-4C are schematic cross-sectional views of a dual damascene structure at various stages of the inventive process ofFIG. 3 ; -
FIG. 4D is a view similar toFIGS. 4A-4C showing the dual damascene structure after copper-filling subsequent to the process ofFIG. 3 ; and -
FIGS. 5A-5D are schematic cross-sectional views of a dual damascene structure at various stages of an alternate inventive barrier layer process. - In accordance with one or more aspects the invention, a barrier layer is formed in a via that has been formed in a dielectric layer on a substrate. The barrier layer may be formed, for example, employing a three-step process. In the first step, a tantalum nitride layer is sputter-deposited on a bottom, side walls and field region of the via. In the second step, the tantalum nitride layer is back sputtered from the bottom of the via to reduce or eliminate the bottom tantalum nitride layer, and to improve side wall coverage. In the third step, a brief or “flash” sputter-deposition of tantalum is performed to provide suitable wetting for subsequent copper seed layer deposition. Other aspects are provided.
-
FIG. 3 is a flow chart that illustrates an exemplary process performed in accordance with the present invention. The process ofFIG. 3 may be performed, for example, in a sputtering reactor of the type illustrated inFIG. 1B . - The process of
FIG. 3 begins with astep 330, at which a tantalum nitride layer is sputter-deposited by a reactive sputtering process. That is, referring toFIG. 1B , the target 14 (a tantalum target) is energized by means of theDC power supply 22. Argon is flowed to thechamber 12 via themass flow controller 26, and nitrogen is flowed to thechamber 12 via themass flow controller 29. In one embodiment of the invention, the chamber pressure may be about 10 mTorr or less, and more preferably in the range of about 2-4 mTorr. Other pressures may be employed. If thereactor 10′ is adapted to process 200 millimeter substrates, the power signal supplied to thetarget 14 by theDC power supply 22 may be about 20 kW (or less), and a bias signal in the range 0-150 W may be supplied to thepedestal 18 by theRF power supply 32. If thereactor 10′ is adapted to process 300 millimeter substrates, the target power may be about 40 kW (or less) and the bias power may be in the range of about 0-300 W. Other power ranges may be employed. In at least one embodiment of the invention, thecoil 38 is not energized duringstep 330. - The energized
target 14 ignites the gases in thechamber 12 to form a plasma so that tantalum nitride is reactively sputter-deposited on thesubstrate 16. In one particular embodiment, step 330 may have a duration in the range of about 7-10 seconds (although other durations may be employed). -
FIG. 4A is a schematic cross-sectional view showing adual damascene structure 300′ upon completion ofstep 330.Reference numeral 400 indicates a tantalum nitride layer deposited duringstep 330.FIG. 4A shows thesame dielectric layer 304,trench 306, vias 308, viabottoms 310, viaside walls 312 andfield region 318 as were referred to in connection withFIG. 2 . LikeFIG. 2 (and alsoFIGS. 4B-4D ),FIG. 4A is not drawn to scale. In one or more embodiments of the invention, upon completion ofstep 330, thetantalum nitride layer 400 may have a thickness on thefield region 318 of greater than about 200 angstroms, and preferably about 220 angstroms. Thicknesses in the range of about 100-400 angstroms may also be employed. - Referring again to
FIG. 3 ,step 330 is followed bystep 332. Atstep 332 thetantalum layer 400 is at least partially back sputtered from the viabottoms 310. In one embodiment of the invention, substantially all of thetantalum nitride layer 400 is back sputtered from the viabottoms 310. Instep 332, argon is flowed to thechamber 12 via themass flow controller 26, but nitrogen is not flowed to thechamber 12. In one or more embodiments of the invention, the pressure in thechamber 12 may be, for example, less than about 10 mTorr and more preferably in the range of about 1-3 mTorr. A bias signal is supplied to thepedestal 18 by theRF power supply 32. If thereactor 10′ is adapted to process 200 millimeter wafers, the bias signal may be, for example, in the range of about 200-500 W, and in one embodiment may be about 300 W. If thereactor 10′ is adapted to process 300 millimeter substrates, the bias signal may be, for example, in the range of about 400-1000 W. In addition, thecoil 38 may be energized by the RF power source 40 (e.g., at about 2 MHz), for example, at a power level in the range of about 1000-3000 W. In addition, thetarget 14 may be energized with a power level in the range of about 0-1000 W. A plasma which is ignited in thechamber 12 causes back sputtering of thetantalum nitride layer 400 from the viabottom walls 310. Depending on the power levels employed, the duration of theback sputtering step 332 may be in the range of about 5-15 seconds. Other chamber pressures, pedestal biases, coil powers, target powers and/or back sputter durations may be employed. -
FIG. 4B is a view similar toFIG. 4A , showing the condition of thedual damascene structure 300′ upon completion ofstep 332. As shown inFIG. 4B , the viabottoms 310 may be substantially free of thetantalum nitride layer 400 upon completion ofstep 332. In addition, coverage/uniformity of the viaside walls 312 with tantalum nitride may be improved. In one embodiment, the thickness of thetantalum nitride layer 400 at thefield region 318 may be reduced from about 220 angstroms to about 200 angstroms upon completion ofstep 332. More generally, the back sputtering step may (1) substantially eliminate the tantalum nitride layer on thebottoms 310 of the vias 308 (thereby improving the contact resistance of any interconnect formed therein); (2) increase the thickness and/or uniformity of the tantalum nitride layer on theside walls 312 of the vias 308 (thereby improving the diffusion resistance of the tantalum nitride barrier layer); and/or (3) only slightly thin the tantalum nitride layer on the field region 318 (thereby maintaining adequate diffusion resistance for the dielectric layer 304). - Referring again to
FIG. 3 ,step 334 followsstep 332. At step 334 a brief (so-called “flash”) sputter-deposition of a tantalum layer is performed. Duringstep 334, argon is flowed to thechamber 12 via themass flow controller 26, but nitrogen is not flowed to thechamber 12. The pressure in thechamber 12 duringstep 334 may be, for example, less than about 10 mTorr and more preferably in the range of about 1-3 mTorr. Thecoil 38 need not be energized duringstep 334, and the target and bias power levels may be similar to those described in connection withstep 330. The duration ofstep 334 may be less than about two seconds, and, in one embodiment, may be in the range of about 1-1.5 seconds. Thus, duringstep 334, thetarget 14 is energized and a plasma is ignited in thechamber 12 to perform sputter-deposition of a tantalum layer on thedual damascene structure 300′. Other chamber pressures, pedestal biases, coil powers, target powers and/or durations may be employed. -
FIG. 4C illustrates thedual damascene structure 300′ upon completion ofstep 334.Reference numeral 402 indicates the tantalum layer deposited duringstep 334. It should again be noted thatFIG. 4C is not drawn to scale. In one particular embodiment of the invention, thetantalum layer 402 may have, upon completion ofstep 334, a thickness in the range of about 30-50 angstroms on thefield region 318. The thickness of thetantalum layer 402 on the viabottom walls 310 may be in the range of about 20-40 angstroms. The side-wall coverage may be about 10 angstroms. Other thicknesses may be employed. Also the target power duringstep 334 may be less than indicated above (e.g., the target power may be about 5 kW or less) in which case thestep 334 may have a longer duration. - It will be appreciated that the controller 30 (
FIG. 1B ) may be programmed to perform one or more of the steps of the process ofFIG. 3 within thereactor 10′. - While the present invention has been described as applied in a plasma sputtering reactor of the type illustrated in
FIG. 1B , it will be understood that the present invention may be applied in other types of plasma sputtering reactors, including those illustrated inFIGS. 1A, 1C and 1D. However, the reactor ofFIG. 1B is believed to be particularly advantageous in view of the back sputtering efficiency promoted by energizing thecoil 38. -
FIG. 4D is a view similar toFIG. 4A , showing thedual damascene structure 300′ upon completion of copper fill and planarization processes that may be performed after the process ofFIG. 3 . In accordance with conventional practices, the filling of thedual damascene structure 300′ with copper may include sputter-deposition of a copper seed layer on the substrate 403 (e.g., in a different reactor than that employed for tantalum nitride and tantalum deposition), followed by copper electrochemical deposition (e.g., electrochemical plating). InFIG. 4D ,reference numeral 404 indicates the copper fill of thedual damascene structure 300′ after formation of a barrier layer that includes thetantalum nitride layer 400 and thetantalum layer 402. - The present invention also may provide a fourth step for the process of
FIG. 3 , in which back sputtering is performed with respect to the tantalum layer 402 (e.g., to further reduce interconnect resistance). However, it may be advantageous to omit back sputtering of the tantalum layer, so that there is adequate wetting of the viabottoms 310. - The thicknesses of the
tantalum nitride layer 400 and thetantalum layer 402 on thefield region 318 as described (e.g., about 200 angstroms of tantalum nitride after back sputtering and about 30-50 angstroms of tantalum) may be suitable in conjunction with a 0.13 micron generation of semiconductor devices, in which a typical via width may be about 0.18 microns, and a typical aspect ratio of a via may be in the range of about 4:1 to 6:1. In general however, the thickness of the tantalum nitride layer on the field region, either before or after back sputtering, may be in the range of about 100-400 angstroms, and the thickness of the tantalum layer on the field region may be any thickness less than about 100 angstroms. It is also contemplated to employ the tantalum nitride and tantalum layer thicknesses according to the present invention in connection with via widths that are less than 0.18 microns. - The inventive methods and apparatus disclosed herein provide for satisfactory barrier layer side wall coverage with reduced asymmetry, together with suitable wetting for subsequent deposition of a copper seed layer.
- The foregoing description discloses only exemplary embodiments of the invention; modifications of the above-disclosed apparatus and methods which fall within the scope of the invention will be readily apparent to those or ordinary skill in the art.
- For instance, one or more of the steps of the process of
FIG. 3 may be implemented in computer program code as one or more computer program products. Each inventive computer program product may be carried by a medium readable by a computer (e.g., a carrier wave signal, a floppy disk, a hard drive, a random access memory, etc.). Such computer program code and/or computer program products may be executed, for example, by one or more of thecontrollers FIGS. 1A-1D . - It may be desirable to control (via the
controllers FIGS. 1A-1D ) the temperature of a substrate during back sputtering (e.g., to prevent excessive heating during back sputtering). This may be achieved, for example, via control of a resistive heating element (not shown) and/or a liquid cooling system (not shown) associated with thepedestal - It is contemplated to modify the process of
FIG. 3 by omitting theback sputtering step 332 performed between the sputter-deposition steps tantalum layer 402 and thetantalum nitride layer 400 after the sputter-deposition of thetantalum layer 402 atstep 334. - As another alternative for modifying the process of
FIG. 3 , a step of sputter-depositing an initial tantalum layer (e.g., with a field region thickness of 100 angstroms or more) is performed afterstep 330 and beforestep 332. Atstep 332, substantially all of the resulting tantalum and tantalum nitride layers may be removed from the via bottoms. Step 334 is then performed as described above. - For example,
FIGS. 5A-5D are cross-sectional views of adual damascene structure 300″ at various stages of such an alternate process. For clarity purposes, no asymmetry in layer thickness is shown inFIGS. 5A-5D . - With reference to
FIG. 5A andFIG. 3 , atantalum nitride layer 500 is deposited on thebottoms 310 andside walls 312 of the vias 308 (Step 330,FIG. 3 ). An initial tantalum layer 501 (FIG. 5B ) then is deposited over the tantalum nitride layer 500 (step not shown inFIG. 3 ). Thereafter, both thetantalum layer 501 and thetantalum nitride layer 500 are back sputtered from thebottoms 310 of the vias 308 (thereby improving barrier layer coverage on the side walls 312), as shown inFIG. 5C (and/or Step 332 ofFIG. 3 ). A thintantalum flash layer 502 then may be formed over the bottom and/or side walls of the vias 308 (FIG. 5D and/orStep 334 inFIG. 3 ). Thedual damascene structure 300″ then may be filled and/or planarized as previously described (e.g., via use of a copper seed layer and/or electrochemical deposition). - In at least one embodiment of the invention, when the inventive alternative process described above is employed with vias having widths of about 0.18 microns or less, the
tantalum nitride layer 500 may have a thickness of about 50-100 angstroms on thefield region 318 of thedielectric layer 304, a thickness of about 10-20 angstroms on theside walls 312 of thevias 308 and a thickness of about 10-70 angstroms on thebottoms 310 of thevias 308. Theinitial tantalum layer 501 may have a thickness of about 100-300 angstroms on thefield region 318 of thedielectric layer 304, a thickness of about 20-40 angstroms on theside walls 312 of thevias 308 and a thickness of about 30-180 angstroms on thebottoms 310 of thevias 308. Following back sputtering of the tantalum nitride andtantalum layers side walls 312 may be about 50 Å or more (and may include a tantalum nitride/tantalum/tantalum nitride stack). Thetantalum flash layer 502 may add a thickness of about 50-100 angstroms (of tantalum) on thefield region 318, a thickness of about 5-15 angstroms on theside walls 312 and a thickness of about 15-50 angstroms on thebottoms 310. Note that thetantalum flash layer 502 is optional, and if employed, may result inside walls 312 having barrier layers of tantalum nitride/tantalum/tantalum nitride/tantalum. Other thicknesses may be employed for the tantalum and tantalum nitride layers. - When back sputtering the tantalum nitride and/or tantalum layers in accordance with the present invention, it may be preferable to maintain a significant neutral metal density (e.g., by sputtering target atoms during back sputtering) and ion density (e.g., by applying power to an RF coil or by employing any other known means for increasing ion density) during back sputtering. Maintaining a significant neutral metal density during back sputtering may reduce and/or prevent over etching of bevel regions 506 (
FIGS. 4A and 5A ) of thedual damascene structure 300″ through deposition of new tantalum and/or tantalum nitride on bevel surfaces during back sputtering. Neutral metal atoms may not, in general, reach thebottoms 310 of thevias 308. A significant ion density (whether metal or argon) will aid in back sputtering of material from thebottoms 310 of thevias 308 by increasing the directionality of the back sputter process. - While the present invention has been described primarily with reference to dual damascene structures, it will be understood that the invention may be applied to other interconnect configurations such as single or triple damascene structures.
- As used herein, a high density plasma physical vapor deposition (HDPPVD) chamber may include any PVD chamber capable of sustaining a plasma having an ion density of at least 1010 ions/cm3 in a bulk region of the plasma (e.g., a region, between a target/cathode and substrate support pedestal, that is not immediately adjacent the target/cathode; although an area immediately adjacent the target/cathode also may have an ion density of at least 1010 ions/cm3).
- Accordingly, while the present invention has been disclosed in connection with exemplary embodiments thereof, it should be understood that other embodiments may fall within the spirit and scope of the invention, as defined by the following claims.
Claims (12)
1. A plasma sputtering reactor, comprising:
a sealable chamber;
a pedestal adapted to support a substrate within the chamber;
a tantalum sputtering target in opposition to the pedestal; and
a controller adapted to control the reactor to:
sputter-deposit a tantalum nitride layer on a substrate having:
a metal feature formed on the substrate;
a dielectric layer formed over the metal feature; and
a via formed in the dielectric layer so as to expose the metal feature, the via having side walls and a bottom, and a width of about 0.18 microns or less;
wherein the tantalum nitride layer is deposited on the side walls and bottom of the via and on a field region of the dielectric layer; and
wherein the tantalum nitride layer has a thickness of at least about 200 angstroms on the field region of the dielectric layer upon completion of the sputter-depositing of the tantalum nitride layer; and
sputter-deposit a tantalum layer on the substrate, the tantalum layer having a thickness of less than about 100 angstroms on the field region of the dielectric layer upon completion of the sputter-depositing of the tantalum layer.
2. The reactor of claim 1 , wherein the tantalum layer has a thickness of less than about 80 angstroms on the field region of the dielectric layer upon completion of the sputter-deposition of the tantalum layer.
3. The reactor of claim 2 , wherein the tantalum layer has a thickness of about 30-50 angstroms on the field region of the dielectric layer upon completion of the sputter-deposition of the tantalum layer.
4. The reactor of claim 3 , wherein the controller controls the reactor to back sputter at least a portion of the tantalum nitride layer from the bottom of the via of the substrate prior to the sputter-deposition of the tantalum layer.
5. The reactor of claim 4 , further comprising a coil disposed within the chamber and surrounding a portion of an interior volume of the chamber, the controller adapted to energize the coil during at least a portion of the back sputtering of the tantalum nitride layer.
6. A plasma sputtering reactor, comprising:
a sealable chamber;
a pedestal adapted to support a substrate within the chamber;
a tantalum sputtering target in opposition to the pedestal; and
a controller adapted to control the reactor to:
sputter-deposit a tantalum nitride layer on a substrate having:
a metal feature formed on the substrate;
a dielectric layer formed over the metal feature; and
a via formed in the dielectric layer so as to expose the metal feature, the via having side walls and a bottom, and a width of about 0.18 microns or less;
wherein the tantalum nitride layer is deposited on the side walls and bottom of the via and on a field region of the dielectric layer; and
wherein the tantalum nitride layer has a thickness of at least about 200 angstroms on the field region of the dielectric layer upon completion of the sputter-depositing of the tantalum nitride layer; and
back sputter at least a portion of the tantalum nitride layer from the bottom of the via of the substrate; and
after the back sputter step, sputter-deposit a tantalum layer on the substrate, the tantalum layer having a thickness of less than about 100 angstroms on the field region of the dielectric layer upon completion of the sputter-depositing of the tantalum layer.
7. The reactor of claim 6 , wherein the tantalum layer has a thickness of less than about 80 angstroms on the field region of the dielectric layer upon completion of the sputter-deposition of the tantalum layer.
8. The reactor of claim 7 , wherein the tantalum layer has a thickness of about 30-50 angstroms on the field region of the dielectric layer upon completion of the sputter-deposition of the tantalum layer.
9. The reactor of claim 6 , wherein the controller controls the reactor to:
sputter-deposit an initial tantalum layer on the substrate prior to the back sputtering of the tantalum nitride layer; and
back sputter at least a portion of the initial tantalum layer sputter-deposited prior to the back sputtering of the tantalum nitride layer.
10. The reactor of claim 6 , wherein the back sputtering of the tantalum nitride layer is performed so as to remove substantially all of the tantalum nitride layer from the bottom of the via.
11. A high density plasma physical vapor deposition (HDPPVD) chamber, comprising:
a sealable chamber;
a pedestal adapted to support a substrate within the chamber;
a tantalum sputtering target in opposition to the pedestal; and
a controller adapted to control the reactor to:
sputter deposit a tantalum nitride layer on the substrate having:
a metal feature formed on the substrate;
a dielectric layer formed over the metal feature; and
a via formed in the dielectric layer so as to expose the metal feature, the via having side walls and a bottom, and a width of about 0.18 microns or less;
wherein the tantalum nitride layer is deposited on the side walls and bottom of the via and on a field region of the dielectric layer;
wherein the tantalum nitride layer has a thickness of at least about 200 angstroms on the field region of the dielectric layer upon completion of the sputter-depositing of the tantalum nitride layer; and
wherein the sputter depositing of the tantalum nitride layer is performed within the HDPPVD chamber employing a plasma having an ion density of at least 1010 ions/cm3, at a pressure of not more than about 10 mTorr using a target power of not more than about 40 kW and a pedestal bias power of not more than about 300 W;
back sputter at least a portion of the tantalum nitride layer from a bottom of the via of the substrate within the HDPPVD chamber at a pressure of not more than about 10 mTorr using a target power of not more than about 1000 W, and a pedestal bias power of not more than about 1000 W; and
sputter-deposit a tantalum layer on the substrate at a pressure of not more than about 10 mTorr using a target power of not more than about 40 kW and a pedestal bias power of not more than about 300 W.
12. The HDPPVD chamber of claim 11 further comprising a coil disposed within the chamber and surrounding a portion of an interior volume of the chamber, the controller adapted to energize the coil during at least a portion of the back sputtering of the tantalum nitride layer, wherein the controller is adapted to apply a coil power of about 1000-3000 W to the coil during the back sputter of the tantalum nitride layer.
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US20080173538A1 (en) * | 2007-01-19 | 2008-07-24 | Kim Sun-Oo | Method and apparatus for sputtering |
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CN106611742B (en) | 2015-10-26 | 2020-05-08 | 中芯国际集成电路制造(上海)有限公司 | Method for forming contact hole |
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Also Published As
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US20030216037A1 (en) | 2003-11-20 |
US6887786B2 (en) | 2005-05-03 |
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