WO2003056619A2 - Selective deposition of a barrier layer on a dielectric material - Google Patents
Selective deposition of a barrier layer on a dielectric material Download PDFInfo
- Publication number
- WO2003056619A2 WO2003056619A2 PCT/US2002/040179 US0240179W WO03056619A2 WO 2003056619 A2 WO2003056619 A2 WO 2003056619A2 US 0240179 W US0240179 W US 0240179W WO 03056619 A2 WO03056619 A2 WO 03056619A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- tantalum
- containing precursor
- seem
- reducing gas
- barrier layer
- Prior art date
Links
Classifications
-
- 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
-
- 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 at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic System or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/3205—Deposition of non-insulating-, e.g. conductive- or resistive-, layers on insulating layers; After-treatment of these layers
-
- 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
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/22—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
- C23C16/30—Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
- C23C16/34—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
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/455—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
- C23C16/45523—Pulsed gas flow or change of composition over time
- C23C16/45525—Atomic layer deposition [ALD]
-
- 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 at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic System or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/28—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 System
- H01L21/28556—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 System by chemical means, e.g. CVD, LPCVD, PECVD, laser CVD
- H01L21/28562—Selective deposition
-
- 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
Definitions
- Embodiments of the present invention relate generally to a method of barrier layer formation.
- Integrated circuits have evolved into complex devices that can include millions of components (e.g., transistors, capacitors and resistors) on a single chip.
- components e.g., transistors, capacitors and resistors
- the evolution of chip designs continually requires faster circuitry and greater circuit densities.
- the demand for greater circuit densities necessitates a reduction in the dimensions of the integrated circuit components.
- the dimensions of the integrated circuit components are reduced (e.g., sub-micron dimensions), the materials used to fabricate such components contribute to the electrical performance thereof.
- low resistivity metal interconnects e.g., aluminum (Al) and copper (Cu)
- Al aluminum
- Cu copper
- the metal interconnects 2 are typically electrically isolated from each other by a bulk insulating material 4.
- a bulk insulating material 4 When the distance between adjacent metal interconnects 2 and/or the thickness of the bulk insulating material 4 has sub-micron dimensions, capacitive coupling occurs between such interconnects 2. Capacitive coupling between adjacent metal interconnects 2 may cause cross-talk and/or resistance-capacitance (RC) delay, which degrades the overall performance of the integrated circuit.
- RC resistance-capacitance
- low dielectric constant bulk insulating materials 4 e.g., dielectric constants less than about 3.5
- low dielectric constant bulk insulating materials 4 include silicon dioxide (Si02), silicate glass and organosilicate glass, among others.
- a barrier layer 6 often separates the metal interconnects 2 from the bulk insulating material 4.
- the barrier layer 6 minimizes the diffusion of the metal from the metal interconnects 2 into the bulk insulating material 4. Diffusion of the metal from the metal interconnects 2 into the bulk insulating material 4 is undesirable because such diffusion can affect the electrical performance of the integrated circuit (e.g., cross-talk and/or RC delay) or render it inoperable.
- barrier materials include refractory metals such as titanium (Ti), tantalum (Ta) and tungsten (W), among others and refractory metal nitrides such as titanium nitride (TiN), tantalum nitride (TaN) and tungsten nitride (WN), among others.
- refractory metals such as titanium (Ti), tantalum (Ta) and tungsten (W)
- refractory metal nitrides such as titanium nitride (TiN), tantalum nitride (TaN) and tungsten nitride (WN), among others.
- Barrier materials are typically deposited using physical vapor deposition
- PVD physical vapor deposition
- CVD chemical vapor deposition
- a method to selectively deposit a barrier layer on dielectric material that surrounds one or more metal interconnects on a substrate is described.
- the barrier layer may comprise a refractory metal nitride such as, for example, tantalum nitride (TaN).
- TaN tantalum nitride
- the barrier layer is selectively deposited on the metal film using a cyclical deposition process including a predetermined number of deposition cycles followed by a purge step.
- each deposition cycle comprises alternately adsorbing a refractory metal-containing precursor and a reducing gas on the dielectric material formed on the substrate in a process chamber.
- the refractory metal-containing precursor and the reducing gas react to form the barrier layer on the dielectric material.
- the process chamber is purged of both the refractory metal- containing precursor and the reducing gas. This deposition sequence of performing a predetermined number of deposition cycles followed by a process chamber purge may be repeated until a desired barrier layer thickness is achieved.
- the predetermined number of deposition cycles is selected to take advantage of differences in the number of deposition cycles needed to start depositing the barrier material on different types of material layers.
- the predetermined number of deposition cycles is advantageously selected to start deposition of the barrier material on the dielectric material but be less than the number of deposition cycles needed to start deposition of such barrier material on the metal interconnects.
- barrier material is only deposited on the dielectric material without being deposited on any metal interconnects.
- the selective deposition of the barrier layer is compatible with integrated circuit fabrication processes. In one integrated circuit fabrication process, the barrier layer is used in a damascene structure.
- a preferred process sequence includes providing a substrate with one or more dielectric material layers thereon having vias defined therethrough to metal features.
- a barrier layer is selectively deposited on the dielectric material using a cyclic deposition process in which a predetermined number of deposition cycles, each comprising alternately adsorbing a refractory metal-containing precursor and a reducing gas on the dielectric material, is followed by a process chamber purge step. The cyclical deposition process is repeated until a desired thickness for the barrier layer is achieved.
- the damascene structure is completed by filling the vias with a conductive material.
- FIG. 1 is a cross-sectional view of a metal interconnect structure including a barrier layer formed on both metal interconnects and bulk insulating material;
- FIG. 2 depicts a schematic cross-sectional view of a process chamber that can be used to perform a cyclical deposition process as described herein;
- FIG. 3 illustrates a process sequence incorporating selective deposition of a barrier layer on a dielectric material using a cyclical deposition process according to one embodiment described herein;
- FIG. 4 illustrates a process sequence incorporating selective deposition of a barrier layer on a dielectric material using a cyclical deposition process according to an alternate embodiment described herein;
- FIG. 5A is a graph showing the number of deposition cycles needed to start forming a tantalum nitride layer on dielectric material as compared to the number of deposition cycles needed to start forming a tantalum nitride layer on copper;
- FIG. 5B is a graph showing the number of deposition cycles needed to start forming a tantalum nitride layer on both silicon oxide and copper at a temperature of about 200 0C;
- FIG. 5C is a graph showing the number of deposition cycles needed to start forming a tantalum nitride layer on silicon oxide as a function of the process chamber pressure.
- FIGS. 6A-6C depict cross-sectional views of a substrate at different stages of an interconnect fabrication process.
- FIG. 2 depicts a schematic cross-sectional view of a process chamber 36 that can be used to perform a cyclical deposition process in accordance with embodiments described herein.
- the process chamber 36 generally houses a wafer support pedestal 148, which is used to support a substrate (not shown).
- the wafer support pedestal 148 is movable in a vertical direction inside the process chamber 36 using a displacement mechanism 148a.
- the substrate can be heated to some desired temperature prior to or during deposition.
- the wafer support pedestal 148 may be heated using an embedded heater element 152a.
- the wafer support pedestal 148 may be resistively heated by applying an electric current from an AC power supply 152 to the heater element 152a.
- the substrate (not shown) is, in turn, heated by the pedestal 148.
- the wafer support pedestal 148 may be heated using radiant heaters, such as, for example, lamps (not shown).
- a temperature sensor 150a such as a thermocouple, is also embedded in the wafer support pedestal 148 to monitor the temperature of the pedestal 148 in a conventional manner. The measured temperature is used in a feedback loop to control the AC power supply 152 for heating element 152a, such that the substrate temperature can be maintained or controlled at a desired temperature which is suitable for a particular process application.
- a vacuum pump 118 is used to evacuate the process chamber 36 and to maintain the pressure inside the process chamber 36.
- a gas manifold 134 through which process gases are introduced into the process chamber 36, is located above the wafer support pedestal 148.
- the gas manifold 134 is connected to a gas panel 111 , which controls and supplies various process gases to the process chamber 36.
- gas manifold 134 Proper control and regulation of the gas flows to the gas manifold 134 are performed by mass flow controllers (not shown) and a microprocessor controller 154.
- the gas manifold 134 allows process gases to be introduced and uniformly distributed in the process chamber 36. Additionally, the gas manifold 134 may optionally be heated to prevent condensation of any reactive gases within the manifold.
- the gas manifold 134 includes a plurality of electronic control valves (not shown).
- the electronic control valves as used herein refer to any control valve capable of providing rapid and precise gas flow to the process chamber 36 with valve open and close cycles of less than about 1-2 seconds, and more preferably less than about 0.1 second.
- the microprocessor controller 154 may be one of any form of general purpose computer processor (CPU) 171 that can be used in an industrial setting for controlling various chambers and sub-processors.
- the computer may use any suitable memory 172, such a random access memory, read only memory, floppy disk drive, hard disk, or any other form of digital storage, local or remote.
- Various support circuits 173 may be coupled to the CPU for supporting the processor in a conventional manner. Software routines as required may be stored in the memory or executed by a second CPU that is remotely located.
- the software routines are executed to initiate process recipes or sequences.
- the software routines when executed, transform the general purpose computer into a specific process computer that controls the chamber operation so that a chamber process is performed.
- software routines may be used to precisely control the activation of the electronic control valves for the execution of process sequences according to the present invention.
- the software routines may be performed in hardware, as an application specific integrated circuit or other type of hardware implementation, or combination of software or hardware.
- a method to selectively deposit a barrier layer on a dielectric layer formed on a substrate is described.
- the barrier layer may comprise a refractory metal nitride, such as, for example, tantalum nitride (TaN), among others.
- the barrier layer is selectively deposited on the dielectric layer using a cyclical deposition process including a predetermined number of deposition cycles followed by a purge step.
- each deposition cycle comprises alternately adsorbing a refractory metal-containing precursor and a reducing gas on the dielectric layer formed on the substrate in a process chamber.
- the refractory metal-containing precursor and the reducing gas react to form the barrier layer on the metal film.
- the process chamber is purged of both the refractory metal- containing precursor and the reducing gas. This deposition sequence of performing a predetermined number of deposition cycles followed by a process chamber purge may be repeated until a desired barrier layer thickness is achieved.
- the predetermined number of deposition cycles is selected to take advantage of differences in the number of deposition cycles needed to start depositing the barrier material on different types of material layers.
- the predetermined number of deposition cycles is advantageously selected to start deposition of the barrier material on the dielectric layer, but be less than the number of deposition cycles needed to start deposition of such barrier material on metal films adjacent thereto.
- FIG. 3 illustrates a process sequence 200 according to the present invention detailing the various steps used for the selective deposition of a barrier layer on a dielectric layer utilizing a constant carrier gas flow. These steps may be performed in a process chamber similar to that described above with reference to FIG. 2.
- a substrate is introduced into a process chamber.
- the substrate may be, for example, a silicon substrate having thereon one or more copper features surrounded by a dielectric material layer.
- the process chamber conditions such as, for example, the temperature and pressure are adjusted to enhance the selective deposition of the barrier material on the dielectric material layer and impede deposition of the barrier material on the metal film.
- a carrier gas stream is established within the process chamber, as indicated in step 204.
- Carrier gases may be selected so as to also act as a purge gas for removal of volatile reactants and/or by-products from the process chamber.
- Carrier gases such as, for example, helium (He), argon (Ar), nitrogen (N2) and hydrogen (H2), as well as combinations thereof, among others, may be used.
- a pulse of the refractory metal-containing precursor is added to the carrier gas stream.
- the term pulse as used herein refers to a dose of material injected into the process chamber or into the carrier gas stream.
- the pulse may comprise one injection of the refractory metal-containing precursor or several short, sequential injections.
- the pulse of the refractory metal-containing precursor lasts for a predetermined time interval.
- suitable tantalum-containing precursors may include, for example, pentakis(dimethylamido) tantalum (PDMAT), pentakis(diethylamido) tantalum (PDEAT), pentakis(ethylmethylamido) tantalum (PEMAT), t-butylamino tris(methylethylamido) tantalum (TBTMET), t-butylamino tris(dimethylamido) tantalum (TBTDMT), bis(cyclopentadienyl) tantalum trihydride, bis(methylcyclopentadienyl) tantalum trihydride and t-butylamino tris(diethylamido) tantalum (TBTDET), among others
- the time interval for the pulse of the refractory metal-containing precursor is variable depending on a number of factors such as, for example, the volume capacity of the process chamber employed, the vacuum system coupled thereto and the volatility/reactivity of the reactants used.
- the process conditions are advantageously selected so that at least a monolayer of the refractory metal-containing precursor may be adsorbed on the dielectric layer, without adsorption of the refractory metal-containing precursor on adjacent metal films. Thereafter, excess refractory metal-containing precursor remaining in the process chamber may be removed therefrom by the constant carrier gas stream in combination with the vacuum system.
- step 208 after excess refractory metal-containing precursor has been sufficiently removed from the process chamber by the carrier gas stream to prevent co-reaction or particle formation with a subsequently provided process gas, a pulse of a reducing gas is added to the carrier gas stream.
- suitable reducing gases include, for example, ammonia (NH3), hydrazine (N2H4), methyl hydrazine (CH3N2H3), dimethyl hydrazine (C2H6N2H2), t-butyl hydrazine (C4H9N2H3), phenyl hydrazine (C6H5N2H3), 2,2'-azoisobutane ((CH3)6C2N2) and ethylazide (C2H5N3), among others.
- the pulse of the reducing gas also lasts for a predetermined time interval.
- the time interval for the pulse of the reducing gas should be long enough to provide a sufficient amount of the reducing gas for reaction with the refractory metal-containing precursor that is already adsorbed on the dielectric layer. Thereafter, excess reducing gas is flushed from the process chamber by the carrier gas stream in combination with the vacuum system.
- Steps 204 through 208 comprise one embodiment of a deposition cycle for the barrier layer.
- a constant flow of the carrier gas is provided to the process chamber modulated by alternating periods of pulsing and non-pulsing where the periods of pulsing alternate between the refractory metal- containing precursor and the reducing gas along with the carrier gas stream, while the periods of non-pulsing include only the carrier gas stream.
- the time interval for each of the pulses of the refractory metal-containing precursor and the reducing gas may have the same duration. That is, the duration of the pulse of the refractory metal-containing precursor may be identical to the duration of the pulse of the reducing gas.
- a time interval (T1) for the pulse of the refractory metal-containing precursor is equal to a time interval (T2) for the pulse of the reducing gas.
- the time interval for each of the pulses of the refractory metal- containing precursor and the reducing gas may have different durations. That is, the duration of the pulse of the refractory metal-containing precursor may be shorted or longer than the duration of the pulse of the reducing gas.
- the time interval (T1 ) for the pulse of the refractory metal-containing precursor is different than the time interval (T2) for the pulse of the reducing gas.
- the periods of non-pulsing between each of the pulses of the refractory metal-containing precursor and the reducing gas may have the same duration.
- the duration of the period of non-pulsing between each pulse of the refractory metal-containing precursor and each pulse of the reducing gas may be identical.
- a time interval (T3) of non-pulsing between the pulse of the refractory metal-containing precursor and the pulse of the reducing gas is equal to a time interval (T4) of non-pulsing between the pulse of the reducing gas and the pulse of the refractory metal-containing precursor.
- the periods of non-pulsing between each of the pulses of the refractory metal-containing precursor and the reducing gas may have different durations. That is, the duration of the period of non-pulsing between each pulse of the refractory metal-containing precursor and each pulse of the reducing gas may be shorter or longer than the duration of the period of non-pulsing between each pulse of the reducing gas and each pulse of the refractory metal-containing precursor.
- a time interval (T3) of non-pulsing between the pulse of the refractory metal-containing precursor and the pulse of the reducing gas is different from a time interval (T4) of non-pulsing between the pulse of the reducing gas and the pulse of the refractory metal-containing precursor.
- T3 of non-pulsing between the pulse of the refractory metal-containing precursor and the pulse of the reducing gas is different from a time interval (T4) of non-pulsing between the pulse of the reducing gas and the pulse of the refractory metal-containing precursor.
- time intervals for each pulse of the refractory metal- containing precursor, the reducing gas and the periods of non-pulsing therebetween for each deposition cycle may have the same duration.
- a time interval (T1 ) for the pulse of the refractory metal-containing precursor may have the same duration as the time interval (T1) for the pulse of the refractory metal-containing precursor in subsequent deposition cycles (C2...CN).
- each pulse of the reducing gas as well as the periods of non-pulsing between the pulses of the refractory metal-containing precursor and the reducing gas in the first deposition cycle (C1) may have the same duration as each pulse of the reducing gas and the periods of non-pulsing between the pulses of the refractory metal-containing precursor and the reducing gas in subsequent deposition cycles (C2...CN), respectively.
- the time interval for at least one pulse of the refractory metal- containing precursor, the reducing gas and the periods of non-pulsing therebetween for one or more of the deposition cycles of the barrier layer deposition process may have different durations.
- the time interval (T1 ) for the pulse of the refractory metal-containing precursor may be longer or shorter than the time interval (T1 ) for the pulse of the refractory metal-containing precursor in subsequent deposition cycles (C2...CN).
- the duration of one or more pulse of the reducing gas or the periods of non-pulsing between the pulses of the refractory metal-containing precursor and the reducing gas in deposition cycle (C1 ) may be longer or shorter than the duration of corresponding pulses of the reducing gas or the periods of non-pulsing between the pulses of the refractory metal-containing precursor and the reducing gas in subsequent deposition cycles (C2...CN), respectively.
- the total number of deposition cycles performed is determined. If a predetermined number of deposition cycles have not been performed, steps 204 through 208 are repeated until such predetermined number of deposition cycles have been completed.
- the process chamber is purged of both the refractory metal-containing precursor and the reducing gas, as indicated by step 212.
- the process chamber may be purged using the carrier gas stream.
- additional predetermined numbers of deposition cycles (steps 203 through 208) may be performed until a desired thickness for the barrier layer is achieved as indicated by step 214, or ended as indicated by step 216.
- the predetermined number of deposition cycles is selected to start depositing barrier material on the dielectric layer within the first few deposition cycles, but be less than the number of deposition cycles needed to start depositing such barrier material on the adjacent metal film. Limiting the number of deposition cycles to a predetermined number that is less than the number needed to start deposition of the barrier material on the adjacent metal film and than purging the process chamber, permits selective deposition of the barrier material only on the dielectric layer.
- a barrier layer deposition sequence 300 includes introducing a substrate into the process chamber (step 302), providing a pulse of a carrier gas to the process chamber (step 304), providing a pulse of a refractory metal-containing precursor to the process chamber (step 306), providing a pulse of a carrier gas to the process chamber (step 308), providing a pulse of a reducing gas to the process chamber (step 310), and repeating steps 304 through 310 until a predetermined number of deposition cycles are performed (step 312).
- the process chamber is purged of both the refractory metal-containing precursor and the reducing gas (step 314).
- additional predetermined numbers of deposition cycles may be performed until a desired thickness for the barrier layer is achieved (step 316), or ended (step 318).
- the time intervals for each of the pulses of the refractory metal-containing precursor, the reducing gas and the carrier gas may have the same or different durations as discussed above with respect to FIG. 3.
- corresponding time intervals for one or more pulses of the refractory metal-containing precursor, the reducing gas and the carrier gas in one or more of the deposition cycles of the barrier layer deposition process may have different durations.
- the barrier layer deposition cycle is depicted as beginning with a pulse of the refractory metal-containing precursor followed by a pulse of the reducing gas.
- the barrier layer deposition cycle may start with a pulse of the reducing gas followed by a pulse of the refractory metal-containing precursor.
- a pulse may comprise one injection of a gas or several short, sequential injections.
- One exemplary deposition cycle for selectively forming a tantalum nitride barrier layer on silicon oxide dielectric material that is adjacent to copper features comprises sequentially providing pulses of pentakis(ethylmethylamido) tantalum (PEMAT) and pulses of ammonia (NH3) to a process chamber similar to that described above with reference to FIG. 2.
- PEMAT pentakis(ethylmethylamido) tantalum
- NH3 ammonia
- argon may be provided to an appropriate flow control valve, for example an electronic flow control valve, at a flow rate of between about 100 seem (standard cubic centimeters per second) to about 1000 seem, preferably at about 500 seem, and thereafter pulsed for about 5 seconds to about 25 seconds, preferably for about 15 seconds.
- the pentakis(ethylmethylamido) tantalum may be provided to an appropriate flow control valve, for example an electronic flow control valve, by flowing hydrogen (H2) at a flow rate of between 30 seem to about 1500 seem, preferably at about 100 seem through an ampoule containing liquid PEMAT at a temperature of about 50 0C to about 95 0C, and thereafter pulsed for about 5 seconds to about 50 seconds, preferably for about 15 seconds.
- H2 hydrogen
- Argon is than provided at a flow rate of between about 100 seem to about 1000 seem, preferably at about 500 seem, and thereafter pulsed for about 5 seconds to about 25 seconds, preferably for about 15 seconds.
- the ammonia may be provided to an appropriate flow control valve, for example an electronic flow control valve, at a flow rate of between about 150 seem to about 700 seem, preferably for about 250 seem, and thereafter pulsed for about 3 seconds to about 45 seconds, preferably for about 5 seconds.
- the substrate may be maintained at a temperature between about 150 0C to about 350 0C, preferably at about 200 0C, at a chamber pressure of up to about 40 torr, preferably at about 0.5 torr.
- the process chamber is purged by providing a flow of the carrier gas thereto.
- FIG. 5A is a plot illustrating the number of deposition cycles needed to start forming a tantalum nitride layer on dielectric oxides as compared to the number of deposition cycles needed to start forming a tantalum nitride layer on copper.
- Each deposition cycle was performed at a substrate temperature of about 225 0C, a deposition chamber pressure of about 0.5 torr, a pentakis(ethylmethylamido) tantalum flow of about 100 seem with hydrogen (H2) that is pulsed for about 15 seconds, an ammonia (NH3) flow of 250 seem that is pulsed for about 5 seconds and an argon (Ar) flow of about 500 seem that is pulsed for about 15 seconds between each pulse of the pentakis(ethylmethylamido) tantalum (PEMAT) and each pulse of the ammonia (NH3).
- H2 hydrogen
- NH3 ammonia
- Ar argon
- the tantalum nitride (TaN) starts to deposit on the silicon oxide during a first deposition cycle, as indicated by line 400.
- the tantalum nitride (TaN) starts to deposit on the fluorosilicate glass (FSG) during a fifth deposition cycle, as indicated by line 405.
- FSG fluorosilicate glass
- the tantalum nitride starts to deposit on the copper during the fourteenth deposition cycle, as indicated by line 410.
- TaN tantalum nitride
- FSG fluorosilicate glass
- the number of deposition cycles needed to start forming a tantalum nitride (TaN) layer on material layers may vary as a function of the substrate temperature.
- a tantalum nitride (TaN) layer was formed on both silicon oxide and copper at a substrate temperature of 200 OC.
- Each deposition cycle was performed at a deposition chamber pressure of about 0.5 torr, a pentakis(ethylmethylamido) tantalum flow of about 100 seem with hydrogen (H2) that is pulsed for about 15 seconds, an ammonia (NH3) flow of 250 seem that is pulsed for about 5 seconds and an argon (Ar) flow of about 500 seem that is pulsed for about 15 seconds between each pulse of the pentakis(ethylmethylamido) tantalum (PEMAT) and each pulse of the ammonia (NH3).
- H2 hydrogen
- NH3 ammonia
- Ar argon
- FIG. 5B about five deposition cycles were needed to start forming a tantalum nitride (TaN) layer on silicon oxide at a substrate temperature of about 200 0C, as indicated by line 415, as compared to one deposition cycle when the substrate temperature is about 225 0C, as indicated by line 400 (FIG. 5A).
- about forty deposition cycles were needed to start forming a tantalum nitride (TaN) layer on copper at a substrate temperature of about 200 0C, as indicated by line 420, as compared to fourteen deposition cycles when the substrate temperature is about 225 0C, as indicated by line 410 (FIG. 5A).
- the number of deposition cycles needed to start forming a tantalum nitride (TaN) layer on silicon oxide may vary as a function of the process chamber pressure.
- a tantalum nitride (TaN) layer was formed on silicon oxide at a process chamber pressures of 0.5 torr, 1 torr, 2 torr and 6 torr.
- Each deposition cycle was performed at a substrate temperature of about 210 0C, a pentakis(ethylmethylamido) tantalum flow of about 100 seem with hydrogen (H2) that is pulsed for about 15 seconds, an ammonia (NH3) flow of 250 seem that is pulsed for about 5 seconds and an argon (Ar) flow of about 500 seem that is pulsed for about 15 seconds between each pulse of the pentakis(ethylmethylamido) tantalum (PEMAT) and each pulse of the ammonia (NH3).
- H2 hydrogen
- NH3 ammonia
- Ar argon
- FIGS. 6A-6C illustrate schematic cross-sectional views of a substrate 500 at different stages of an integrated circuit fabrication sequence incorporating a tantalum nitride barrier layer formed on dielectric material.
- substrate 500 may correspond to a silicon substrate, or other material layer that has been formed on the substrate 500.
- FIG. 6A illustrates a cross-sectional view of a substrate 500 having conductive leads 501 formed thereon surrounded by a dielectric material 502.
- the conductive leads 501 may be metal (e.g., aluminum (Al) or copper (Cu)).
- the dielectric material 502 may be an oxide (e.g., silicon oxide).
- FIG. 6A illustrates one embodiment in which the substrate 500 is silicon having copper leads 501 formed thereon.
- the copper leads 501 have a thickness of about 5,000 A to about 2 microns depending on the size of the structure to be fabricated.
- a dielectric material 502 surrounds the copper leads 501.
- the dielectric material 502 may be a low dielectric constant silicon oxide layer.
- the dielectric material 502 may have a thickness of up to about 5 microns.
- Vias 503 are defined in the dielectric material 502 to the copper leads 501.
- the vias are defined in the dielectric material 502 using conventional lithography and etching techniques.
- a tantalum nitride barrier layer 505 is selectively formed on the dielectric material 502 comprising the sidewalls of the vias 503.
- the tantalum nitride barrier layer 505 may be formed according to the process parameters described above with respect to FIGS. 3-4.
- the thickness of the tantalum nitride barrier layer 505 should be about 50 A to about 500 A.
- the vias 503 are filled with a conductive material 506 such as aluminum (Al), copper (Cu), tungsten (W), or combinations thereof.
- copper is used to fill the vias 503 due to its low resistivity (resistivity of about 1.7 /cm).
- the conductive material 506 may be deposited using chemical vapor deposition (CVD) techniques, physical vapor deposition techniques (PVD) techniques, electroplating techniques, or combinations thereof.
- CVD chemical vapor deposition
- PVD physical vapor deposition techniques
- electroplating techniques or combinations thereof.
- Formation of the tantalum nitride barrier layer 505 on the dielectric material 502 comprising the sidewalls of the vias 503 advantageously prevents metal migration into such dielectric material when the vias 503 are subsequently filled with the conductive material 506.
- barrier layer 505 only on the sidewalls of the vias 503 minimizes any increase to the overall resistivity of the interconnect structure which would otherwise occur had the barrier material 505 also been deposited on the copper leads 501.
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP02792404A EP1459369A2 (en) | 2001-12-21 | 2002-12-17 | Selective deposition of a barrier layer on a dielectric material |
JP2003557038A JP2005531918A (en) | 2001-12-21 | 2002-12-17 | Selective deposition of barrier layers on dielectric materials. |
KR10-2004-7009891A KR20040068969A (en) | 2001-12-21 | 2002-12-17 | Selective deposition of a barrier layer on a dielectric material |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US34230701P | 2001-12-21 | 2001-12-21 | |
US60/342,307 | 2001-12-21 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2003056619A2 true WO2003056619A2 (en) | 2003-07-10 |
WO2003056619A3 WO2003056619A3 (en) | 2004-03-25 |
Family
ID=23341249
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2002/040179 WO2003056619A2 (en) | 2001-12-21 | 2002-12-17 | Selective deposition of a barrier layer on a dielectric material |
Country Status (6)
Country | Link |
---|---|
US (1) | US6939801B2 (en) |
EP (1) | EP1459369A2 (en) |
JP (1) | JP2005531918A (en) |
KR (1) | KR20040068969A (en) |
CN (1) | CN1319134C (en) |
WO (1) | WO2003056619A2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005281308A (en) * | 2004-03-12 | 2005-10-13 | Rohm & Haas Co | Precursor compound for depositing coating film of ceramic and metal, and method for preparing the same |
Families Citing this family (60)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6974766B1 (en) | 1998-10-01 | 2005-12-13 | Applied Materials, Inc. | In situ deposition of a low κ dielectric layer, barrier layer, etch stop, and anti-reflective coating for damascene application |
US6620723B1 (en) | 2000-06-27 | 2003-09-16 | Applied Materials, Inc. | Formation of boride barrier layers using chemisorption techniques |
US7405158B2 (en) | 2000-06-28 | 2008-07-29 | Applied Materials, Inc. | Methods for depositing tungsten layers employing atomic layer deposition techniques |
US6551929B1 (en) | 2000-06-28 | 2003-04-22 | Applied Materials, Inc. | Bifurcated deposition process for depositing refractory metal layers employing atomic layer deposition and chemical vapor deposition techniques |
US7101795B1 (en) | 2000-06-28 | 2006-09-05 | Applied Materials, Inc. | Method and apparatus for depositing refractory metal layers employing sequential deposition techniques to form a nucleation layer |
US9051641B2 (en) | 2001-07-25 | 2015-06-09 | Applied Materials, Inc. | Cobalt deposition on barrier surfaces |
US8110489B2 (en) | 2001-07-25 | 2012-02-07 | Applied Materials, Inc. | Process for forming cobalt-containing materials |
US20090004850A1 (en) | 2001-07-25 | 2009-01-01 | Seshadri Ganguli | Process for forming cobalt and cobalt silicide materials in tungsten contact applications |
US6916398B2 (en) | 2001-10-26 | 2005-07-12 | Applied Materials, Inc. | Gas delivery apparatus and method for atomic layer deposition |
US7780785B2 (en) | 2001-10-26 | 2010-08-24 | Applied Materials, Inc. | Gas delivery apparatus for atomic layer deposition |
US7081271B2 (en) | 2001-12-07 | 2006-07-25 | Applied Materials, Inc. | Cyclical deposition of refractory metal silicon nitride |
US6911391B2 (en) | 2002-01-26 | 2005-06-28 | Applied Materials, Inc. | Integration of titanium and titanium nitride layers |
US6833161B2 (en) | 2002-02-26 | 2004-12-21 | Applied Materials, Inc. | Cyclical deposition of tungsten nitride for metal oxide gate electrode |
US6972267B2 (en) | 2002-03-04 | 2005-12-06 | Applied Materials, Inc. | Sequential deposition of tantalum nitride using a tantalum-containing precursor and a nitrogen-containing precursor |
US7279432B2 (en) | 2002-04-16 | 2007-10-09 | Applied Materials, Inc. | System and method for forming an integrated barrier layer |
US7186385B2 (en) | 2002-07-17 | 2007-03-06 | Applied Materials, Inc. | Apparatus for providing gas to a processing chamber |
US7211508B2 (en) | 2003-06-18 | 2007-05-01 | Applied Materials, Inc. | Atomic layer deposition of tantalum based barrier materials |
DE102004015174A1 (en) * | 2004-03-27 | 2005-10-13 | Aixtron Ag | Process for separating in particular metal oxides by means of non-continuous precursor injection |
US20050252449A1 (en) | 2004-05-12 | 2005-11-17 | Nguyen Son T | Control of gas flow and delivery to suppress the formation of particles in an MOCVD/ALD system |
US8323754B2 (en) | 2004-05-21 | 2012-12-04 | Applied Materials, Inc. | Stabilization of high-k dielectric materials |
US7241686B2 (en) | 2004-07-20 | 2007-07-10 | Applied Materials, Inc. | Atomic layer deposition of tantalum-containing materials using the tantalum precursor TAIMATA |
TWI329135B (en) | 2005-11-04 | 2010-08-21 | Applied Materials Inc | Apparatus and process for plasma-enhanced atomic layer deposition |
US7798096B2 (en) | 2006-05-05 | 2010-09-21 | Applied Materials, Inc. | Plasma, UV and ion/neutral assisted ALD or CVD in a batch tool |
US7775508B2 (en) | 2006-10-31 | 2010-08-17 | Applied Materials, Inc. | Ampoule for liquid draw and vapor draw with a continuous level sensor |
US7678298B2 (en) | 2007-09-25 | 2010-03-16 | Applied Materials, Inc. | Tantalum carbide nitride materials by vapor deposition processes |
US7585762B2 (en) | 2007-09-25 | 2009-09-08 | Applied Materials, Inc. | Vapor deposition processes for tantalum carbide nitride materials |
US7824743B2 (en) | 2007-09-28 | 2010-11-02 | Applied Materials, Inc. | Deposition processes for titanium nitride barrier and aluminum |
US20100062149A1 (en) | 2008-09-08 | 2010-03-11 | Applied Materials, Inc. | Method for tuning a deposition rate during an atomic layer deposition process |
US8491967B2 (en) | 2008-09-08 | 2013-07-23 | Applied Materials, Inc. | In-situ chamber treatment and deposition process |
US8146896B2 (en) | 2008-10-31 | 2012-04-03 | Applied Materials, Inc. | Chemical precursor ampoule for vapor deposition processes |
US20100119734A1 (en) * | 2008-11-07 | 2010-05-13 | Applied Materials, Inc. | Laminar flow in a precursor source canister |
US9330939B2 (en) * | 2012-03-28 | 2016-05-03 | Applied Materials, Inc. | Method of enabling seamless cobalt gap-fill |
JP6488284B2 (en) | 2013-09-27 | 2019-03-20 | アプライド マテリアルズ インコーポレイテッドApplied Materials,Incorporated | How to enable seamless cobalt gap filling |
WO2016071531A1 (en) * | 2014-11-07 | 2016-05-12 | T-Touch International S.À.R.L. | Selective dielectric coating |
WO2016120957A1 (en) * | 2015-01-26 | 2016-08-04 | 株式会社日立国際電気 | Semiconductor-device manufacturing method, substrate treating apparatus, and recording medium |
US10002789B2 (en) | 2016-03-24 | 2018-06-19 | International Business Machines Corporation | High performance middle of line interconnects |
US10242866B2 (en) * | 2017-03-08 | 2019-03-26 | Lam Research Corporation | Selective deposition of silicon nitride on silicon oxide using catalytic control |
US10622214B2 (en) | 2017-05-25 | 2020-04-14 | Applied Materials, Inc. | Tungsten defluorination by high pressure treatment |
KR102405723B1 (en) | 2017-08-18 | 2022-06-07 | 어플라이드 머티어리얼스, 인코포레이티드 | High pressure and high temperature annealing chamber |
US10276411B2 (en) | 2017-08-18 | 2019-04-30 | Applied Materials, Inc. | High pressure and high temperature anneal chamber |
SG11202003355QA (en) | 2017-11-11 | 2020-05-28 | Micromaterials Llc | Gas delivery system for high pressure processing chamber |
CN111432920A (en) | 2017-11-17 | 2020-07-17 | 应用材料公司 | Condenser system for high pressure processing system |
WO2019173006A1 (en) | 2018-03-09 | 2019-09-12 | Applied Materials, Inc. | High pressure annealing process for metal containing materials |
CN111936664A (en) | 2018-03-19 | 2020-11-13 | 应用材料公司 | Method for depositing a coating on an aerospace component |
EP3784815A4 (en) | 2018-04-27 | 2021-11-03 | Applied Materials, Inc. | Protection of components from corrosion |
US10950429B2 (en) | 2018-05-08 | 2021-03-16 | Applied Materials, Inc. | Methods of forming amorphous carbon hard mask layers and hard mask layers formed therefrom |
CN110610897B (en) * | 2018-06-15 | 2022-02-22 | 北京北方华创微电子装备有限公司 | Manufacturing process of diffusion barrier layer in copper interconnection structure and copper interconnection structure |
US10748783B2 (en) | 2018-07-25 | 2020-08-18 | Applied Materials, Inc. | Gas delivery module |
US11009339B2 (en) | 2018-08-23 | 2021-05-18 | Applied Materials, Inc. | Measurement of thickness of thermal barrier coatings using 3D imaging and surface subtraction methods for objects with complex geometries |
US11114382B2 (en) | 2018-10-19 | 2021-09-07 | International Business Machines Corporation | Middle-of-line interconnect having low metal-to-metal interface resistance |
US10636705B1 (en) | 2018-11-29 | 2020-04-28 | Applied Materials, Inc. | High pressure annealing of metal gate structures |
WO2020117462A1 (en) | 2018-12-07 | 2020-06-11 | Applied Materials, Inc. | Semiconductor processing system |
US10903111B2 (en) | 2019-03-20 | 2021-01-26 | International Business Machines Corporation | Semiconductor device with linerless contacts |
EP3959356A4 (en) | 2019-04-26 | 2023-01-18 | Applied Materials, Inc. | Methods of protecting aerospace components against corrosion and oxidation |
US11794382B2 (en) | 2019-05-16 | 2023-10-24 | Applied Materials, Inc. | Methods for depositing anti-coking protective coatings on aerospace components |
US11697879B2 (en) | 2019-06-14 | 2023-07-11 | Applied Materials, Inc. | Methods for depositing sacrificial coatings on aerospace components |
US11466364B2 (en) | 2019-09-06 | 2022-10-11 | Applied Materials, Inc. | Methods for forming protective coatings containing crystallized aluminum oxide |
US11901222B2 (en) | 2020-02-17 | 2024-02-13 | Applied Materials, Inc. | Multi-step process for flowable gap-fill film |
US11519066B2 (en) | 2020-05-21 | 2022-12-06 | Applied Materials, Inc. | Nitride protective coatings on aerospace components and methods for making the same |
EP4175772A1 (en) | 2020-07-03 | 2023-05-10 | Applied Materials, Inc. | Methods for refurbishing aerospace components |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0798778A2 (en) * | 1996-03-25 | 1997-10-01 | Kabushiki Kaisha Toshiba | Method of manufacturing a semiconductor device of multilayer wire structure |
US6025243A (en) * | 1989-09-26 | 2000-02-15 | Canon Kabushiki Kaisha | Method for preparing a semiconductor device |
WO2001015220A1 (en) * | 1999-08-24 | 2001-03-01 | Asm America, Inc. | Method for bottomless deposition of barrier layers in integrated circuit metallization schemes |
US6281072B1 (en) * | 1998-05-11 | 2001-08-28 | Micron Technology, Inc. | Multiple step methods for forming conformal layers |
Family Cites Families (73)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FI118158B (en) | 1999-10-15 | 2007-07-31 | Asm Int | Process for modifying the starting chemical in an ALD process |
FI117944B (en) | 1999-10-15 | 2007-04-30 | Asm Int | A method for growing transition metal nitride thin films |
FI57975C (en) * | 1979-02-28 | 1980-11-10 | Lohja Ab Oy | OVER ANCHORING VIDEO UPDATE FOR AVAILABILITY |
US4389973A (en) * | 1980-03-18 | 1983-06-28 | Oy Lohja Ab | Apparatus for performing growth of compound thin films |
US6084302A (en) * | 1995-12-26 | 2000-07-04 | Micron Technologies, Inc. | Barrier layer cladding around copper interconnect lines |
US6342277B1 (en) * | 1996-08-16 | 2002-01-29 | Licensee For Microelectronics: Asm America, Inc. | Sequential chemical vapor deposition |
US5916365A (en) * | 1996-08-16 | 1999-06-29 | Sherman; Arthur | Sequential chemical vapor deposition |
US5923056A (en) * | 1996-10-10 | 1999-07-13 | Lucent Technologies Inc. | Electronic components with doped metal oxide dielectric materials and a process for making electronic components with doped metal oxide dielectric materials |
US6287965B1 (en) * | 1997-07-28 | 2001-09-11 | Samsung Electronics Co, Ltd. | Method of forming metal layer using atomic layer deposition and semiconductor device having the metal layer as barrier metal layer or upper or lower electrode of capacitor |
KR100385946B1 (en) * | 1999-12-08 | 2003-06-02 | 삼성전자주식회사 | Method for forming a metal layer by an atomic layer deposition and a semiconductor device with the metal layer as a barrier metal layer, an upper electrode, or a lower electrode of capacitor |
KR100269306B1 (en) * | 1997-07-31 | 2000-10-16 | 윤종용 | Integrate circuit device having buffer layer containing metal oxide stabilized by low temperature treatment and fabricating method thereof |
KR100261017B1 (en) * | 1997-08-19 | 2000-08-01 | 윤종용 | Method for forming metal wiring of semiconductor device |
US6197683B1 (en) * | 1997-09-29 | 2001-03-06 | Samsung Electronics Co., Ltd. | Method of forming metal nitride film by chemical vapor deposition and method of forming metal contact of semiconductor device using the same |
US6348376B2 (en) * | 1997-09-29 | 2002-02-19 | Samsung Electronics Co., Ltd. | Method of forming metal nitride film by chemical vapor deposition and method of forming metal contact and capacitor of semiconductor device using the same |
FI104383B (en) * | 1997-12-09 | 2000-01-14 | Fortum Oil & Gas Oy | Procedure for coating the inside of a plant |
KR100269328B1 (en) * | 1997-12-31 | 2000-10-16 | 윤종용 | Method for forming conductive layer using atomic layer deposition process |
US6015917A (en) * | 1998-01-23 | 2000-01-18 | Advanced Technology Materials, Inc. | Tantalum amide precursors for deposition of tantalum nitride on a substrate |
NL1009327C2 (en) | 1998-06-05 | 1999-12-10 | Asm Int | Method and device for transferring wafers. |
KR100319888B1 (en) * | 1998-06-16 | 2002-01-10 | 윤종용 | Method of forming selective metal layer and method of forming capacitor and filling contact hole using the same |
KR100275738B1 (en) * | 1998-08-07 | 2000-12-15 | 윤종용 | Method for producing thin film using atomatic layer deposition |
KR20000022003A (en) | 1998-09-10 | 2000-04-25 | 이경수 | Method for forming three-components compound comprising metal and silicon |
KR100287180B1 (en) * | 1998-09-17 | 2001-04-16 | 윤종용 | Method for manufacturing semiconductor device including metal interconnection formed using interface control layer |
KR100327328B1 (en) * | 1998-10-13 | 2002-05-09 | 윤종용 | Method for forming dielectric layer of capacitor having partially different thickness in the layer |
KR100297719B1 (en) * | 1998-10-16 | 2001-08-07 | 윤종용 | Method for manufacturing thin film |
US6305314B1 (en) * | 1999-03-11 | 2001-10-23 | Genvs, Inc. | Apparatus and concept for minimizing parasitic chemical vapor deposition during atomic layer deposition |
US6540838B2 (en) * | 2000-11-29 | 2003-04-01 | Genus, Inc. | Apparatus and concept for minimizing parasitic chemical vapor deposition during atomic layer deposition |
US6200893B1 (en) * | 1999-03-11 | 2001-03-13 | Genus, Inc | Radical-assisted sequential CVD |
US6124158A (en) * | 1999-06-08 | 2000-09-26 | Lucent Technologies Inc. | Method of reducing carbon contamination of a thin dielectric film by using gaseous organic precursors, inert gas, and ozone to react with carbon contaminants |
KR20010017820A (en) | 1999-08-14 | 2001-03-05 | 윤종용 | Semiconductor device and manufacturing method thereof |
US6511539B1 (en) | 1999-09-08 | 2003-01-28 | Asm America, Inc. | Apparatus and method for growth of a thin film |
DE10049257B4 (en) | 1999-10-06 | 2015-05-13 | Samsung Electronics Co., Ltd. | Process for thin film production by means of atomic layer deposition |
FI117942B (en) | 1999-10-14 | 2007-04-30 | Asm Int | Process for making oxide thin films |
US6902763B1 (en) | 1999-10-15 | 2005-06-07 | Asm International N.V. | Method for depositing nanolaminate thin films on sensitive surfaces |
AU1088401A (en) | 1999-10-15 | 2001-04-30 | Asm Microchemistry Oy | Deposition of transition metal carbides |
US6475276B1 (en) * | 1999-10-15 | 2002-11-05 | Asm Microchemistry Oy | Production of elemental thin films using a boron-containing reducing agent |
JP5173098B2 (en) | 1999-10-15 | 2013-03-27 | エーエスエム インターナショナル エヌ.ヴェー. | Conformal lining layer for damascene metallization |
US6203613B1 (en) * | 1999-10-19 | 2001-03-20 | International Business Machines Corporation | Atomic layer deposition with nitrate containing precursors |
KR20010047128A (en) | 1999-11-18 | 2001-06-15 | 이경수 | Method of vaporizing a liquid source and apparatus used therefor |
US6780704B1 (en) * | 1999-12-03 | 2004-08-24 | Asm International Nv | Conformal thin films over textured capacitor electrodes |
KR100624903B1 (en) * | 1999-12-22 | 2006-09-19 | 주식회사 하이닉스반도체 | Method of manufacturing a capacitor in a semiconductor device |
KR100705926B1 (en) * | 1999-12-22 | 2007-04-11 | 주식회사 하이닉스반도체 | Method of manufacturing a capacitor in a semiconductor device |
FI20000099A0 (en) * | 2000-01-18 | 2000-01-18 | Asm Microchemistry Ltd | A method for growing thin metal films |
AU2001245388A1 (en) * | 2000-03-07 | 2001-09-17 | Asm America, Inc. | Graded thin films |
KR100363088B1 (en) * | 2000-04-20 | 2002-12-02 | 삼성전자 주식회사 | Method of manufacturing barrier metal layer using atomic layer deposition method |
US6482733B2 (en) * | 2000-05-15 | 2002-11-19 | Asm Microchemistry Oy | Protective layers prior to alternating layer deposition |
KR100403611B1 (en) * | 2000-06-07 | 2003-11-01 | 삼성전자주식회사 | Metal-insulator-metal capacitor and manufacturing method thereof |
KR100332313B1 (en) | 2000-06-24 | 2002-04-12 | 서성기 | Apparatus and method for depositing thin film on wafer |
KR100444149B1 (en) * | 2000-07-22 | 2004-08-09 | 주식회사 아이피에스 | ALD thin film depositin equipment cleaning method |
KR100396879B1 (en) * | 2000-08-11 | 2003-09-02 | 삼성전자주식회사 | Semiconductor memory device having capacitor encapsulated by multi-layer which includes double layeres being made of same material and method of manufacturing thereof |
US6613695B2 (en) * | 2000-11-24 | 2003-09-02 | Asm America, Inc. | Surface preparation prior to deposition |
AU2002225761A1 (en) * | 2000-11-30 | 2002-06-11 | Asm America, Inc. | Thin films for magnetic devices |
US6949450B2 (en) * | 2000-12-06 | 2005-09-27 | Novellus Systems, Inc. | Method for integrated in-situ cleaning and subsequent atomic layer deposition within a single processing chamber |
US6416822B1 (en) * | 2000-12-06 | 2002-07-09 | Angstrom Systems, Inc. | Continuous method for depositing a film by modulated ion-induced atomic layer deposition (MII-ALD) |
KR100385947B1 (en) * | 2000-12-06 | 2003-06-02 | 삼성전자주식회사 | Method of forming thin film by atomic layer deposition |
US20020104481A1 (en) * | 2000-12-06 | 2002-08-08 | Chiang Tony P. | System and method for modulated ion-induced atomic layer deposition (MII-ALD) |
US6428859B1 (en) * | 2000-12-06 | 2002-08-06 | Angstron Systems, Inc. | Sequential method for depositing a film by modulated ion-induced atomic layer deposition (MII-ALD) |
US20020197402A1 (en) * | 2000-12-06 | 2002-12-26 | Chiang Tony P. | System for depositing a film by modulated ion-induced atomic layer deposition (MII-ALD) |
US6630201B2 (en) * | 2001-04-05 | 2003-10-07 | Angstron Systems, Inc. | Adsorption process for atomic layer deposition |
US20020076481A1 (en) * | 2000-12-15 | 2002-06-20 | Chiang Tony P. | Chamber pressure state-based control for a reactor |
US20020076507A1 (en) * | 2000-12-15 | 2002-06-20 | Chiang Tony P. | Process sequence for atomic layer deposition |
US20020073924A1 (en) * | 2000-12-15 | 2002-06-20 | Chiang Tony P. | Gas introduction system for a reactor |
US6844604B2 (en) * | 2001-02-02 | 2005-01-18 | Samsung Electronics Co., Ltd. | Dielectric layer for semiconductor device and method of manufacturing the same |
FI109770B (en) * | 2001-03-16 | 2002-10-15 | Asm Microchemistry Oy | Growing transition metal nitride thin films by using compound having hydrocarbon, amino or silyl group bound to nitrogen as nitrogen source material |
US7348042B2 (en) * | 2001-03-19 | 2008-03-25 | Novellus Systems, Inc. | Continuous method for depositing a film by modulated ion-induced atomic layer deposition (MII-ALD) |
US20020144655A1 (en) * | 2001-04-05 | 2002-10-10 | Chiang Tony P. | Gas valve system for a reactor |
US20020144657A1 (en) * | 2001-04-05 | 2002-10-10 | Chiang Tony P. | ALD reactor employing electrostatic chuck |
KR100363332B1 (en) * | 2001-05-23 | 2002-12-05 | Samsung Electronics Co Ltd | Method for forming semiconductor device having gate all-around type transistor |
US6828218B2 (en) * | 2001-05-31 | 2004-12-07 | Samsung Electronics Co., Ltd. | Method of forming a thin film using atomic layer deposition |
US6806145B2 (en) * | 2001-08-31 | 2004-10-19 | Asm International, N.V. | Low temperature method of forming a gate stack with a high k layer deposited over an interfacial oxide layer |
US20030042630A1 (en) * | 2001-09-05 | 2003-03-06 | Babcoke Jason E. | Bubbler for gas delivery |
WO2003025243A2 (en) * | 2001-09-14 | 2003-03-27 | Asm International N.V. | Metal nitride deposition by ald using gettering reactant |
US6960537B2 (en) * | 2001-10-02 | 2005-11-01 | Asm America, Inc. | Incorporation of nitrogen into high k dielectric film |
US6916398B2 (en) * | 2001-10-26 | 2005-07-12 | Applied Materials, Inc. | Gas delivery apparatus and method for atomic layer deposition |
-
2002
- 2002-12-13 US US10/319,788 patent/US6939801B2/en not_active Expired - Fee Related
- 2002-12-17 WO PCT/US2002/040179 patent/WO2003056619A2/en not_active Application Discontinuation
- 2002-12-17 JP JP2003557038A patent/JP2005531918A/en active Pending
- 2002-12-17 CN CNB028281985A patent/CN1319134C/en not_active Expired - Fee Related
- 2002-12-17 KR KR10-2004-7009891A patent/KR20040068969A/en not_active Application Discontinuation
- 2002-12-17 EP EP02792404A patent/EP1459369A2/en not_active Withdrawn
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6025243A (en) * | 1989-09-26 | 2000-02-15 | Canon Kabushiki Kaisha | Method for preparing a semiconductor device |
EP0798778A2 (en) * | 1996-03-25 | 1997-10-01 | Kabushiki Kaisha Toshiba | Method of manufacturing a semiconductor device of multilayer wire structure |
US6281072B1 (en) * | 1998-05-11 | 2001-08-28 | Micron Technology, Inc. | Multiple step methods for forming conformal layers |
WO2001015220A1 (en) * | 1999-08-24 | 2001-03-01 | Asm America, Inc. | Method for bottomless deposition of barrier layers in integrated circuit metallization schemes |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005281308A (en) * | 2004-03-12 | 2005-10-13 | Rohm & Haas Co | Precursor compound for depositing coating film of ceramic and metal, and method for preparing the same |
EP1640475A2 (en) * | 2004-03-12 | 2006-03-29 | Rohm And Haas Company | Precursor compounds for deposition of ceramic and metal films and preparation methods thereof |
EP1640475A3 (en) * | 2004-03-12 | 2006-12-06 | Rohm And Haas Company | Precursor compounds for deposition of ceramic and metal films and preparation methods thereof |
Also Published As
Publication number | Publication date |
---|---|
EP1459369A2 (en) | 2004-09-22 |
US6939801B2 (en) | 2005-09-06 |
US20030224578A1 (en) | 2003-12-04 |
CN1620721A (en) | 2005-05-25 |
WO2003056619A3 (en) | 2004-03-25 |
JP2005531918A (en) | 2005-10-20 |
KR20040068969A (en) | 2004-08-02 |
CN1319134C (en) | 2007-05-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6939801B2 (en) | Selective deposition of a barrier layer on a dielectric material | |
US6809026B2 (en) | Selective deposition of a barrier layer on a metal film | |
US7041335B2 (en) | Titanium tantalum nitride silicide layer | |
US7244683B2 (en) | Integration of ALD/CVD barriers with porous low k materials | |
US7262133B2 (en) | Enhancement of copper line reliability using thin ALD tan film to cap the copper line | |
US7279432B2 (en) | System and method for forming an integrated barrier layer | |
US8114789B2 (en) | Formation of a tantalum-nitride layer | |
US7786006B2 (en) | Interconnect structures with a metal nitride diffusion barrier containing ruthenium and method of forming | |
US7867896B2 (en) | Sequential deposition of tantalum nitride using a tantalum-containing precursor and a nitrogen-containing precursor | |
US7407876B2 (en) | Method of plasma enhanced atomic layer deposition of TaC and TaCN films having good adhesion to copper | |
US20030124262A1 (en) | Integration of ALD tantalum nitride and alpha-phase tantalum for copper metallization application | |
US20020086111A1 (en) | Method of forming refractory metal nitride layers using chemisorption techniques | |
US20080227291A1 (en) | Formation of composite tungsten films | |
US20100151676A1 (en) | Densification process for titanium nitride layer for submicron applications | |
WO2002001628A2 (en) | Formation of boride barrier layers using chemisorption techniques | |
WO2004053947A2 (en) | Titanium silicon nitride (tisin) barrier layer for copper diffusion | |
WO2008055007A2 (en) | Methods of fabricating a barrier layer with varying composition for copper metallization | |
WO2003038892A2 (en) | Atomic-layer-deposited tantalum nitride and alpha-phase tantalum as barrier layers for copper metallization |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A2 Designated state(s): CN JP KR SG |
|
AL | Designated countries for regional patents |
Kind code of ref document: A2 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR IE IT LU MC NL PT SE SK TR |
|
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 2002792404 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2003557038 Country of ref document: JP Ref document number: 1020047009891 Country of ref document: KR |
|
WWE | Wipo information: entry into national phase |
Ref document number: 20028281985 Country of ref document: CN |
|
WWP | Wipo information: published in national office |
Ref document number: 2002792404 Country of ref document: EP |
|
WWW | Wipo information: withdrawn in national office |
Ref document number: 2002792404 Country of ref document: EP |