WO2017100630A1 - In-situ film annealing with spatial atomic layer deposition - Google Patents
In-situ film annealing with spatial atomic layer deposition Download PDFInfo
- Publication number
- WO2017100630A1 WO2017100630A1 PCT/US2016/065906 US2016065906W WO2017100630A1 WO 2017100630 A1 WO2017100630 A1 WO 2017100630A1 US 2016065906 W US2016065906 W US 2016065906W WO 2017100630 A1 WO2017100630 A1 WO 2017100630A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- substrate surface
- gas
- environment
- film
- deposition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
- H10P14/60—Formation of materials, e.g. in the shape of layers or pillars of insulating materials
- H10P14/69—Inorganic materials
- H10P14/692—Inorganic materials composed of oxides, glassy oxides or oxide-based glasses
- H10P14/6921—Inorganic materials composed of oxides, glassy oxides or oxide-based glasses containing silicon
- H10P14/69215—Inorganic materials composed of oxides, glassy oxides or oxide-based glasses containing silicon the material being a silicon oxide, e.g. SiO2
-
- 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
- C23C16/04—Coating on selected surface areas, e.g. using masks
- C23C16/045—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
- 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]
- C23C16/45527—Atomic layer deposition [ALD] characterized by the ALD cycle, e.g. different flows or temperatures during half-reactions, unusual pulsing sequence, use of precursor mixtures or auxiliary reactants or activations
-
- 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
- C23C16/50—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 using electric discharges
-
- 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
- C23C16/56—After-treatment
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
- H10P14/20—Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials
- H10P14/24—Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials using chemical vapour deposition [CVD]
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
- H10P14/60—Formation of materials, e.g. in the shape of layers or pillars of insulating materials
- H10P14/63—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the formation processes
- H10P14/6326—Deposition processes
- H10P14/6328—Deposition from the gas or vapour phase
- H10P14/6334—Deposition from the gas or vapour phase using decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition
- H10P14/6336—Deposition from the gas or vapour phase using decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition in the presence of a plasma [PECVD]
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
- H10P14/60—Formation of materials, e.g. in the shape of layers or pillars of insulating materials
- H10P14/63—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the formation processes
- H10P14/6326—Deposition processes
- H10P14/6328—Deposition from the gas or vapour phase
- H10P14/6334—Deposition from the gas or vapour phase using decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition
- H10P14/6339—Deposition from the gas or vapour phase using decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition deposition by cyclic CVD, e.g. ALD, ALE or pulsed CVD
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
- H10P14/60—Formation of materials, e.g. in the shape of layers or pillars of insulating materials
- H10P14/65—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by treatments performed before or after the formation of the materials
- H10P14/6516—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by treatments performed before or after the formation of the materials of treatments performed after formation of the materials
- H10P14/6529—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by treatments performed before or after the formation of the materials of treatments performed after formation of the materials by exposure to a gas or vapour
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
- H10P14/60—Formation of materials, e.g. in the shape of layers or pillars of insulating materials
- H10P14/65—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by treatments performed before or after the formation of the materials
- H10P14/6516—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by treatments performed before or after the formation of the materials of treatments performed after formation of the materials
- H10P14/6529—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by treatments performed before or after the formation of the materials of treatments performed after formation of the materials by exposure to a gas or vapour
- H10P14/6532—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by treatments performed before or after the formation of the materials of treatments performed after formation of the materials by exposure to a gas or vapour by exposure to a plasma
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
- H10P14/60—Formation of materials, e.g. in the shape of layers or pillars of insulating materials
- H10P14/66—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the type of materials
- H10P14/668—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the type of materials the materials being characterised by the deposition precursor materials
- H10P14/6681—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the type of materials the materials being characterised by the deposition precursor materials the precursor containing a compound comprising Si
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
- H10P14/60—Formation of materials, e.g. in the shape of layers or pillars of insulating materials
- H10P14/66—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the type of materials
- H10P14/668—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the type of materials the materials being characterised by the deposition precursor materials
- H10P14/6681—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the type of materials the materials being characterised by the deposition precursor materials the precursor containing a compound comprising Si
- H10P14/6682—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the type of materials the materials being characterised by the deposition precursor materials the precursor containing a compound comprising Si the compound being a silane, e.g. disilane, methylsilane or chlorosilane
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
- H10P14/60—Formation of materials, e.g. in the shape of layers or pillars of insulating materials
- H10P14/66—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the type of materials
- H10P14/668—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the type of materials the materials being characterised by the deposition precursor materials
- H10P14/6681—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the type of materials the materials being characterised by the deposition precursor materials the precursor containing a compound comprising Si
- H10P14/6687—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the type of materials the materials being characterised by the deposition precursor materials the precursor containing a compound comprising Si the compound comprising silicon and nitrogen
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P95/00—Generic processes or apparatus for manufacture or treatments not covered by the other groups of this subclass
- H10P95/90—Thermal treatments, e.g. annealing or sintering
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10W—GENERIC PACKAGES, INTERCONNECTIONS, CONNECTORS OR OTHER CONSTRUCTIONAL DETAILS OF DEVICES COVERED BY CLASS H10
- H10W10/00—Isolation regions in semiconductor bodies between components of integrated devices
- H10W10/01—Manufacture or treatment
- H10W10/011—Manufacture or treatment of isolation regions comprising dielectric materials
- H10W10/014—Manufacture or treatment of isolation regions comprising dielectric materials using trench refilling with dielectric materials, e.g. shallow trench isolations
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10W—GENERIC PACKAGES, INTERCONNECTIONS, CONNECTORS OR OTHER CONSTRUCTIONAL DETAILS OF DEVICES COVERED BY CLASS H10
- H10W10/00—Isolation regions in semiconductor bodies between components of integrated devices
- H10W10/10—Isolation regions comprising dielectric materials
- H10W10/17—Isolation regions comprising dielectric materials formed using trench refilling with dielectric materials, e.g. shallow trench isolations
Definitions
- the present disclosure relates generally to methods of depositing thin films.
- the disclosure relates to processes for the deposition of films by spatial ALD with in-situ annealing.
- STI shallow trench isolation
- Spatial Atomic Layer Deposition uses a sequence of atomic layer deposition and plasma etch which enables void free fill in trenches at reasonable productivity.
- thermal ALD and PE ALD can be used to provide conformal void free deposition.
- PEALD plasma enhanced
- thermal ALD has uniform film quality in structure, average film quality is relatively poor that requires additional post processes such as steam anneal and UV- cures.
- PEALD can provide good film quality especially on the top part of surface feature but not throughout the filled trenches due to nature of plasma distribution. Thus, also requiring post processes. The additional post treatment processes add extra cost to overall device processes.
- One or more embodiments of the disclosure are directed to processing methods comprising exposing a substrate surface having at least one feature thereon to a deposition environment to deposit a film.
- the substrate surface is exposed to an anneal environment to improve a property of the film.
- Additional embodiments of the disclosure are directed to processing methods comprising positioning a substrate surface in a processing chamber.
- the substrate surface has at least one feature thereon.
- the at least one feature creates a gap with a bottom, top and sidewalls.
- the substrate surface is exposed to a deposition environment comprising at least one cycle of a silicon precursor and an oxygen containing reactant to form a silicon oxide film on the at least one feature.
- the substrate surface is exposed to an anneal environment to improve a wet etch rate ratio of the silicon oxide film. Exposure to the deposition environment and, optionally, the anneal environment, is repeated to fill the gap of the feature.
- FIG. 1 For embodiments of the disclosure are directed to processing method comprising placing a substrate having a substrate surface with a feature into a processing chamber.
- the processing chamber comprises a plurality of process regions with each process region separated from adjacent process regions by a gas curtain. At least a portion of the substrate surface is exposed to a first process condition in a first process region of the processing chamber.
- the first process condition comprises a silicon precursor.
- the substrate surface is laterally moved through a gas curtain to a second process region of the processing chamber.
- the substrate surface is exposed to a second process condition in the second process region of the processing chamber.
- the second process condition comprises an oxygen-containing reactant to form a silicon oxide film.
- the substrate surface is laterally moved through a gas curtain to a third process region of the processing chamber.
- the substrate surface is exposed to a third process condition in the third process region of the processing chamber.
- the third process condition comprises an anneal environment. Exposure to the first process condition and the second process condition is repeated to fill the feature.
- FIG. 1 shows a cross-sectional view of a batch processing chamber in accordance with one or more embodiment of the disclosure
- FIG. 2 shows a partial perspective view of a batch processing chamber in accordance with one or more embodiment of the disclosure
- FIG. 3 shows a schematic view of a batch processing chamber in accordance with one or more embodiment of the disclosure
- FIG. 4 shows a schematic view of a portion of a wedge shaped gas distribution assembly for use in a batch processing chamber in accordance with one or more embodiment of the disclosure
- FIG. 5 shows a schematic view of a batch processing chamber in accordance with one or more embodiment of the disclosure.
- FIGS. 6A and 6B show SEM images of Samples A and B, respectively. DETAILED DESCRIPTION
- a "substrate” as used herein, refers to any substrate or material surface formed on a substrate upon which film processing is performed during a fabrication process.
- a substrate surface on which processing can be performed include materials such as silicon, silicon oxide, strained silicon, silicon on insulator (SOI), carbon doped silicon oxides, amorphous silicon, doped silicon, germanium, gallium arsenide, glass, sapphire, and any other materials such as metals, metal nitrides, metal alloys, and other conductive materials, depending on the application.
- Substrates include, without limitation, semiconductor wafers. Substrates may be exposed to a pretreatment process to polish, etch, reduce, oxidize, hydroxylate, anneal and/or bake the substrate surface.
- any of the film processing steps disclosed may also be performed on an under-layer formed on the substrate as disclosed in more detail below, and the term "substrate surface" is intended to include such under-layer as the context indicates.
- substrate surface is intended to include such under-layer as the context indicates.
- the terms "precursor”, “reactant”, “reactive gas” and the like are used interchangeably to refer to any gaseous species that can react with the substrate surface.
- Some embodiments of the disclosure are directed to processes that use a reaction chamber with multiple gas inlet channels that can be used for introduction of different chemicals or plasma gases. Spatially, these channels are separated by inert purging gases and/or vacuum pumping holes to create a gas curtain that minimizes or eliminates mixing of gases from different channels to avoid unwanted gas phase reactions. Wafers moving through these different spatially separated channels get sequential and multiple surface exposures to different chemical or plasma environment so that layer by layer film growth in spatial ALD mode or surface etching process occur.
- the processing chamber has modular architectures on gas distribution components and each modular component has independent parameter control (e.g., RF or gas flow) to provide flexibility to control, for example, gas flow and/or RF exposure.
- Some embodiments of the disclosure use spatial architectures and comprise a first chemistry dosing on a substrate surface followed by a second chemical exposure to react with the dosed chemistry to form a film, followed by a third additional post treatment process.
- embodiments of the disclosure have an ALD layer that can be exposed to in-situ post treatment.
- the treatment is done once.
- the treatment may be employed every cycle. The minimum amount of treatment might be in the range of every 1 to 1 00 deposition cycles or more.
- the film being deposited may determine what type of treatment is used. For instance, in the case of the ALD of Si0 2 using BDEAS and 0 2 plasma, treatment may be performed by employing a steam anneal step using H 2 0 plasma or thermally flowing the H 2 0.
- the water can be delivered as a vapor to the injector by, for example, a bubbler or DLI (direct liquid injection). Controlled water vapor can then be flowed through the injector module which configures gas distribution function and in some cases with plasma capability.
- Embodiments of the disclosure are directed to methods for filling the gap of a semiconductor feature.
- a feature can be trench having a bottom and sidewalls.
- Gap filling deposits a film to fill the trench.
- the substrate is exposed to a precursor and reactant to deposit a film.
- the substrate is then moved to an anneal environment to change at least one of the film parameters.
- the methods of various embodiments allow for the formation of continuous and/or defect-free films with low wet etch rate ratios.
- One or more embodiments of the disclosure are directed to processing methods comprising sequentially exposing a substrate surface to a precursor and a reactant to form a film, and an anneal environment to treat the film.
- the precursor comprises a silicon precursor.
- deposition can be achieved by maximizing the partial pressure of the silicon precursor while minimizing the wafer temperature.
- Suitable silicon precursors include, but are not limited to, bis(diethylamino)silane (BDEAS), tetrakis(dimethylamino)silane (TDMAS) and/or bts ⁇ iertiary-buiy!amino ⁇ siiane (BTBAS).
- the pressure in the processing chamber, or region of the processing chamber can be independently controlled for the precursor exposure, reactant exposure and anneal environment.
- exposure to each of the precursor, reactant and the anneal environment occurs at a pressure in the range of about 50 mTorr to about 200 Torr, or about 50 mTorr to about 100 Torr.
- the silicon precursor is exposed to the substrate at a pressure greater than or equal to about 500 mTorr, or greater than or equal to about 1 Torr, or greater than or equal to about 5 Torr, or greater than or equal to about 10 Torr, or greater than or equal to about 20 Torr, or greater than or equal to about 30 Torr.
- the temperature at which the substrate surface is exposed to the precursor, reactant or anneal environment can be varied depending on, for example, the thermal budget of the device being formed and the precursor. In some embodiments, exposure to each of the precursor, reactant and the anneal environment occurs at a temperature in the range of about 350 Q C to about 700 Q C. In one or more embodiments, the silicon halide precursor is exposed to the substrate at a temperature in the range of about 375 Q C to about 600 Q C, or in the range of about 400 Q C to about 550 Q C. In some embodiments, the deposition temperature is about the same as the anneal temperature. In one or more embodiments, the anneal temperature is maintained within ⁇ 25 Q C of the deposition temperature.
- FIG. 1 shows a cross-section of a processing chamber 1 00 including a gas distribution assembly 120, also referred to as injectors or an injector assembly, and a susceptor assembly 140.
- the gas distribution assembly 120 is any type of gas delivery device used in a processing chamber.
- the gas distribution assembly 120 includes a front surface 121 which faces the susceptor assembly 140.
- the front surface 121 can have any number or variety of openings to deliver a flow of gases toward the susceptor assembly 140.
- the gas distribution assembly 120 also includes an outer edge 124 which in the embodiments shown, is substantially round.
- gas distribution assembly 120 can vary depending on the particular process being used. Embodiments of the disclosure can be used with any type of processing system where the gap between the susceptor and the gas distribution assembly is controlled. While various types of gas distribution assemblies can be employed (e.g., showerheads), embodiments of the disclosure may be particularly useful with spatial gas distribution assemblies which have a plurality of substantially parallel gas channels. As used in this specification and the appended claims, the term "substantially parallel" means that the elongate axis of the gas channels extend in the same general direction. There can be slight imperfections in the parallelism of the gas channels.
- the plurality of substantially parallel gas channels can include at least one first reactive gas A channel, at least one second reactive gas B channel, at least one purge gas P channel and/or at least one vacuum V channel.
- the gases flowing from the first reactive gas A channel(s), the second reactive gas B channel(s) and the purge gas P channel(s) are directed toward the top surface of the wafer. Some of the gas flow moves horizontally across the surface of the wafer and out of the process region through the purge gas P channel(s). A substrate moving from one end of the gas distribution assembly to the other end will be exposed to each of the process gases in turn, forming a layer on the substrate surface.
- the gas distribution assembly 120 is a rigid stationary body made of a single injector unit. In one or more embodiments, the gas distribution assembly 120 is made up of a plurality of individual sectors (e.g., injector units 122), as shown in FIG. 2. Either a single piece body or a multi-sector body can be used with the various embodiments of the disclosure described.
- a susceptor assembly 140 is positioned beneath the gas distribution assembly 1 20.
- the susceptor assembly 140 includes a top surface 141 and at least one recess 142 in the top surface 141 .
- the susceptor assembly 140 also has a bottom surface 143 and an edge 144.
- the recess 142 can be any suitable shape and size depending on the shape and size of the substrates 60 being processed. In the embodiment shown in FIG. 1 , the recess 142 has a flat bottom to support the bottom of the wafer; however, the bottom of the recess can vary.
- the recess has step regions around the outer peripheral edge of the recess which are sized to support the outer peripheral edge of the wafer. The amount of the outer peripheral edge of the wafer that is supported by the steps can vary depending on, for example, the thickness of the wafer and the presence of features already present on the back side of the wafer.
- the recess 142 in the top surface 141 of the susceptor assembly 140 is sized so that a substrate 60 supported in the recess 142 has a top surface 61 substantially coplanar with the top surface 141 of the susceptor 140.
- substantially coplanar means that the top surface of the wafer and the top surface of the susceptor assembly are coplanar within ⁇ 0.2 mm. In some embodiments, the top surfaces are coplanar within ⁇ 0.15 mm, ⁇ 0.10 mm or ⁇ 0.05 mm.
- the susceptor assembly 140 of FIG. 1 includes a support post 160 which is capable of lifting, lowering and rotating the susceptor assembly 140.
- the susceptor assembly may include a heater, or gas lines, or electrical components within the center of the support post 160.
- the support post 160 may be the primary means of increasing or decreasing the gap between the susceptor assembly 140 and the gas distribution assembly 120, moving the susceptor assembly 140 into proper position.
- the susceptor assembly 140 may also include fine tuning actuators 162 which can make micro-adjustments to susceptor assembly 140 to create a predetermined gap 170 between the susceptor assembly 140 and the gas distribution assembly 120.
- the gap 170 distance is in the range of about 0.1 mm to about 5.0 mm, or in the range of about 0.1 mm to about 3.0 mm, or in the range of about 0.1 mm to about 2.0 mm, or in the range of about 0.2 mm to about 1 .8 mm, or in the range of about 0.3 mm to about 1 .7 mm, or in the range of about 0.4 mm to about 1 .6 mm, or in the range of about 0.5 mm to about 1 .5 mm, or in the range of about 0.6 mm to about 1 .4 mm, or in the range of about 0.7 mm to about 1 .3 mm, or in the range of about 0.8 mm to about 1 .2 mm, or in the range of about 0.9 mm to about 1 .1 mm, or about 1 mm.
- the processing chamber 1 00 shown in the Figures is a carousel-type chamber in which the susceptor assembly 140 can hold a plurality of substrates 60.
- the gas distribution assembly 120 may include a plurality of separate injector units 122, each injector unit 122 being capable of depositing a film on the wafer, as the wafer is moved beneath the injector unit.
- Two pie-shaped injector units 122 are shown positioned on approximately opposite sides of and above the susceptor assembly 140. This number of injector units 122 is shown for illustrative purposes only. It will be understood that more or less injector units 122 can be included.
- each of the individual pie-shaped injector units 122 may be independently moved, removed and/or replaced without affecting any of the other injector units 122. For example, one segment may be raised to permit a robot to access the region between the susceptor assembly 140 and gas distribution assembly 120 to load/unload substrates 60.
- Processing chambers having multiple gas injectors can be used to process multiple wafers simultaneously so that the wafers experience the same process flow.
- the processing chamber 100 has four gas injector assemblies and four substrates 60.
- the substrates 60 can be positioned between the injector assemblies 30. Rotating 17 the susceptor assembly 140 by 45 Q will result in each substrate 60 which is between injector assemblies 1 20 to be moved to an injector assembly 120 for film deposition, as illustrated by the dotted circle under the injector assemblies 120. An additional 45 Q rotation would move the substrates 60 away from the injector assemblies 30.
- the number of substrates 60 and gas distribution assemblies 120 can be the same or different.
- the number of wafers being processed are fraction of or an integer multiple of the number of gas distribution assemblies. For example, if there are four gas distribution assemblies, there are 4x wafers being processed, where x is an integer value greater than or equal to one.
- the gas distribution assembly 120 includes eight process regions separated by gas curtains and the susceptor assembly 140 can hold six wafers.
- the processing chamber 100 shown in FIG. 3 is merely representative of one possible configuration and should not be taken as limiting the scope of the disclosure.
- the processing chamber 100 includes a plurality of gas distribution assemblies 120.
- the processing chamber 100 shown is octagonal; however, those skilled in the art will understand that this is one possible shape and should not be taken as limiting the scope of the disclosure.
- the gas distribution assemblies 120 shown are trapezoidal, but can be a single circular component or made up of a plurality of pie-shaped segments, like that shown in FIG. 2.
- the embodiment shown in FIG. 3 includes a load lock chamber 180, or an auxiliary chamber like a buffer station.
- This chamber 1 80 is connected to a side of the processing chamber 100 to allow, for example the substrates (also referred to as substrates 60) to be loaded/unloaded from the chamber 100.
- a wafer robot may be positioned in the chamber 1 80 to move the substrate onto the susceptor.
- Rotation of the carousel can be continuous or intermittent (discontinuous).
- the wafers are constantly rotating so that they are exposed to each of the injectors in turn.
- the wafers can be moved to the injector region and stopped, and then to the region 84 between the injectors and stopped.
- the carousel can rotate so that the wafers move from an inter-injector region across the injector (or stop adjacent the injector) and on to the next inter-injector region where the carousel can pause again. Pausing between the injectors may provide time for additional processing steps between each layer deposition (e.g., exposure to plasma).
- FIG. 4 shows a sector or portion of a gas distribution assembly 220, which may be referred to as an injector unit 122.
- the injector units 122 can be used individually or in combination with other injector units. For example, as shown in FIG. 5, four of the injector units 122 of FIG. 4 are combined to form a single gas distribution assembly 220. (The lines separating the four injector units are not shown for clarity.) While the injector unit 122 of FIG. 4 has both a first reactive gas port 125 and a second gas port 135 in addition to purge gas ports 155 and vacuum ports 145, an injector unit 122 does not need all of these components.
- a gas distribution assembly 220 in accordance with one or more embodiment may comprise a plurality of sectors (or injector units 1 22) with each sector being identical or different.
- the gas distribution assembly 220 is positioned within the processing chamber and comprises a plurality of elongate gas ports 125, 135, 145 in a front surface 1 21 of the gas distribution assembly 220.
- the plurality of elongate gas ports 125, 1 35, 145, 155 extend from an area adjacent the inner peripheral edge 123 toward an area adjacent the outer peripheral edge 124 of the gas distribution assembly 220.
- the plurality of gas ports shown include a first reactive gas port 125, a second gas port 135, a vacuum port 145 which surrounds each of the first reactive gas ports and the second reactive gas ports and a purge gas port 1 55.
- the ports when stating that the ports extend from at least about an inner peripheral region to at least about an outer peripheral region, however, the ports can extend more than just radially from inner to outer regions.
- the ports can extend tangentially as vacuum port 145 surrounds reactive gas port 125 and reactive gas port 135.
- the wedge shaped reactive gas ports 125, 1 35 are surrounded on all edges, including adjacent the inner peripheral region and outer peripheral region, by a vacuum port 145.
- each portion of the substrate surface is exposed to the various reactive gases.
- the substrate will be exposed to, or "see", a purge gas port 155, a vacuum port 145, a first reactive gas port 125, a vacuum port 145, a purge gas port 1 55, a vacuum port 145, a second gas port 1 35 and a vacuum port 145.
- the injector unit 122 shown makes a quarter circle but could be larger or smaller.
- the gas distribution assembly 220 shown in FIG. 5 can be considered a combination of four of the injector units 1 22 of FIG. 4 connected in series.
- the injector unit 122 of FIG. 4 shows a gas curtain 150 that separates the reactive gases.
- gas curtain is used to describe any combination of gas flows or vacuum that separate reactive gases from mixing.
- the gas curtain 150 shown in FIG. 4 comprises the portion of the vacuum port 145 next to the first reactive gas port 125, the purge gas port 155 in the middle and a portion of the vacuum port 145 next to the second gas port 135. This combination of gas flow and vacuum can be used to prevent or minimize gas phase reactions of the first reactive gas and the second reactive gas.
- the combination of gas flows and vacuum from the gas distribution assembly 220 form a separation into a plurality of process regions 250.
- the process regions are roughly defined around the individual gas ports 1 25, 135 with the gas curtain 1 50 between 250.
- the embodiment shown in FIG. 5 makes up eight separate process regions 250 with eight separate gas curtains 150 between.
- a processing chamber can have at least two process region. In some embodiments, there are at least three, four, five, six, seven, eight, nine, 10, 1 1 or 1 2 process regions.
- a substrate may be exposed to more than one process region 250 at any given time.
- the portions that are exposed to the different process regions will have a gas curtain separating the two. For example, if the leading edge of a substrate enters a process region including the second gas port 135, a middle portion of the substrate will be under a gas curtain 1 50 and the trailing edge of the substrate will be in a process region including the first reactive gas port 125.
- a factory interface 280 which can be, for example, a load lock chamber, is shown connected to the processing chamber 100.
- a substrate 60 is shown superimposed over the gas distribution assembly 220 to provide a frame of reference. The substrate 60 may often sit on a susceptor assembly to be held near the front surface 121 of the gas distribution plate 1 20.
- the substrate 60 is loaded via the factory interface 280 into the processing chamber 100 onto a substrate support or susceptor assembly (see FIG. 3).
- the substrate 60 can be shown positioned within a process region because the substrate is located adjacent the first reactive gas port 125 and between two gas curtains 150a, 150b. Rotating the substrate 60 along path 127 will move the substrate counter-clockwise around the processing chamber 100. Thus, the substrate 60 will be exposed to the first process region 250a through the eighth process region 250h, including all process regions between.
- Embodiments of the disclosure are directed to processing methods comprising a processing chamber 1 00 with a plurality of process regions 250a-250h with each process region separated from an adjacent region by a gas curtain 150.
- a processing chamber 1 00 with a plurality of process regions 250a-250h with each process region separated from an adjacent region by a gas curtain 150.
- the processing chamber shown in FIG. 5 The number of gas curtains and process regions within the processing chamber can be any suitable number depending on the arrangement of gas flows.
- the embodiment shown in FIG. 5 has eight gas curtains 1 50 and eight process regions 250a-250h.
- the number of gas curtains is generally equal to or greater than the number of process regions.
- a plurality of substrates 60 are positioned on a substrate support, for example, the susceptor assembly 140 shown FIGS. 1 and 2.
- the plurality of substrates 60 are rotated around the process regions for processing.
- the gas curtains 150 are engaged (gas flowing and vacuum on) throughout processing including periods when no reactive gas is flowing into the chamber.
- a first reactive gas A is flowed into one or more of the process regions 250 while an inert gas is flowed into any process region 250 which does not have a first reactive gas A flowing into it.
- an inert gas would be flowing into process region 250a.
- the inert gas can be flowed through the first reactive gas port 125 or the second gas port 135.
- the inert gas flow within the process regions can be constant or varied.
- the reactive gas is co-flowed with an inert gas.
- the inert gas will act as a carrier and diluent. Since the amount of reactive gas, relative to the carrier gas, is small, co-flowing may make balancing the gas pressures between the process regions easier by decreasing the differences in pressure between adjacent regions.
- one or more embodiments of the disclosure are directed to processing methods utilizing a batch processing chamber like that shown in FIG. 5.
- a substrate 60 is placed into the processing chamber which has a plurality of sections 250, each section separated from adjacent section by a gas curtain 150.
- Some embodiments of the method comprise exposing a substrate surface having a feature thereon to a deposition environment to deposit a film.
- a deposition environment comprises one or more process regions or process conditions that deposit a film.
- the substrate surface is exposed to a first process condition in a first section 250a of the processing chamber.
- the first process condition of some embodiments comprises a silicon precursor to form a silicon layer.
- the substrate surface is laterally moved through a gas curtain 150 to a second section 250b.
- the silicon layer is exposed to a second process condition in the second section 250b.
- the second process condition of some embodiments comprises a reactant that can react with the substrate surface.
- the reactant comprises an oxygen-containing reactant to form an oxide film. Suitable oxygen-containing reactants include, but are not limited to, water, peroxide, carbon dioxide, molecular oxygen and ozone.
- the second process condition comprises a nitrogen-containing compound, for example, molecular nitrogen, ammonia or hydrazine to form a nitride film.
- the substrate surface is laterally moved from the second process region to another process region that may have the first process condition or an annealing environment. As each sequential exposure to the first process condition and the second process condition deposits a layer of film, repeated exposure might deposit multiple layers of the film.
- the deposition environment of some embodiments comprises the first process condition and the second process condition in separate process regions of the processing chamber. Stated differently, the deposition environment of some embodiments comprises the first process region and the second process region including any gas curtains adjacent either or both process regions. In some embodiments, depositing the film comprises repeating the exposure of the substrate surface to the deposition environment to fill the feature. Exposing the substrate surface to the deposition environment includes laterally moving the substrate surface from the first process region having the first process condition to a second process region having the second process condition. In some embodiments, exposure to the deposition environment includes lateral movement of the substrate surface through a gas curtain between the first process region and the second process region.
- an annealing environment is any conditions (e.g., gas, temperature, pressure) that can improve a property of the deposited film.
- the annealing environment may improve the wet etch rate of the deposited film.
- the anneal environment comprises steam (water vapor).
- other gases can be used in the anneal environment. Suitable gases include, but are not limited to, H 2 0 2 , C0 2 , 0 2 , 0 3 and/or H 2 .
- the anneal environment comprises a plasma in which an annealing gas is flowed into. Suitable plasmas include, but are not limited to, Ar, 0 2 , 0 3 and/or N 2 .
- the plasma can be, for example, a direct plasma or remote plasma source and can be, for example, capacitively coupled or inductively coupled.
- the time that the substrate surface is exposed to the anneal environment can be varied. Varying the time may be done by changing the movement speed of the substrate or increasing the size of the anneal environment. In some embodiments, the substrate surface is exposed to the anneal environment for a time in the range of about 30 seconds to about 10 minutes, or about 1 minute to about 8 minutes, or for a time greater than 60 seconds, 90 seconds or 120 seconds.
- the substrate surface can be exposed to additional first process conditions and second process conditions to form a film with a predetermined film thickness.
- the substrate surface is repeatedly exposed to the precursor in one section of the processing chamber, the reactant in one section of the processing chamber and an annealing environment in another section of the processing chamber.
- the first process region 250a and fifth process region 250e may have the first process condition while the second process region 250b and sixth process region 250f has the second process condition and the third process region 250c and seventh process region 250g have an annealing environment.
- the substrate may be exposed to the annealing environment first followed by the first process condition in the second process region.
- the annealing environment is in more than one process region for each first process condition and second process condition.
- the first process region 250a may have the first process condition
- the second process region 250b may have the second process condition
- the third process region 250c and fourth process region 250d may have an annealing environment.
- the gas curtain between the third process region 250c and the fourth process region 250d may be disabled.
- the thickness of the film formed with the precursor and reactant prior to exposure to the anneal environment can be modified.
- the substrate surface is exposed to the annealing environment after formation of a film having a thickness in the range of about 10 A to about 300 A, or about 20 A to about 250 A, or up to about 400 A, or 350 A, or 300 A, or 250 A, or 200 A, or 150 A or 100 A.
- the substrate surface is exposed to the annealing environment after a number of cycles of precursor/reactant exposure, the number in the range of 1 to about 200 cycles, or about 1 to about 100 cycles.
- the anneal environment is disabled so that only an inert gas flows into the process region. This can be done to allow for repeated exposure to the precursor and reactant to grow a film.
- the anneal environment can be turned on and the substrate passed through.
- the precursor/reactant flows are stopped while the anneal environment is created that the substrate can be exposed to longer annealing.
- a silicon oxide film was deposited onto a substrate surface having a trench. After deposition of about 200-300 A of SiO 2 , the wet etch rate in trench was measured using 1 % HF. The wet etch rate ratio (WER), measured relative to a thermal oxide was calculated to be 3.6-1 1 .4 at tighter trenches.
- FIG. 6A shows a SEM image of Sample A.
- FIG. 6B shows a SEM image of Sample B.
- the substrate is subjected to processing prior to and/or after forming the layer.
- This processing can be performed in the same chamber or in one or more separate processing chambers.
- the substrate is moved from the first chamber to a separate, second chamber for further processing.
- the substrate can be moved directly from the first chamber to the separate processing chamber, or it can be moved from the first chamber to one or more transfer chambers, and then moved to the separate processing chamber.
- the processing apparatus may comprise multiple chambers in communication with a transfer station. An apparatus of this sort may be referred to as a "cluster tool" or "clustered system,” and the like.
- a cluster tool is a modular system comprising multiple chambers which perform various functions including substrate center-finding and orientation, annealing, annealing, deposition and/or etching.
- a cluster tool includes at least a first chamber and a central transfer chamber.
- the central transfer chamber may house a robot that can shuttle substrates between and among processing chambers and load lock chambers.
- the transfer chamber is typically maintained at a vacuum condition and provides an intermediate stage for shuttling substrates from one chamber to another and/or to a load lock chamber positioned at a front end of the cluster tool.
- Centura® and the Endura® are the Centura® and the Endura®, both available from Applied Materials, Inc., of Santa Clara, Calif.
- Centura® and the Endura® are the Centura® and the Endura®, both available from Applied Materials, Inc., of Santa Clara, Calif.
- Other processing chambers which may be used include, but are not limited to, cyclical layer deposition (CLD), atomic layer deposition (ALD), chemical vapor deposition (CVD), physical vapor deposition (PVD), etch, pre-clean, chemical clean, thermal treatment such as RTP, plasma nitridation, anneal, orientation, hydroxylation and other substrate processes.
- CLD cyclical layer deposition
- ALD atomic layer deposition
- CVD chemical vapor deposition
- PVD physical vapor deposition
- etch pre-clean
- chemical clean such as RTP, plasma nitridation, anneal, orientation, hydroxylation and other substrate processes.
- the substrate is continuously under vacuum or "load lock” conditions, and is not exposed to ambient air when being moved from one chamber to the next.
- the transfer chambers are thus under vacuum and are "pumped down” under vacuum pressure.
- Inert gases may be present in the processing chambers or the transfer chambers.
- an inert gas is used as a purge gas to remove some or all of the reactants.
- a purge gas is injected at the exit of the deposition chamber to prevent reactants from moving from the deposition chamber to the transfer chamber and/or additional processing chamber. Thus, the flow of inert gas forms a curtain at the exit of the chamber.
- the substrate can be processed in single substrate deposition chambers, where a single substrate is loaded, processed and unloaded before another substrate is processed.
- the substrate can also be processed in a continuous manner, similar to a conveyer system, in which multiple substrate are individually loaded into a first part of the chamber, move through the chamber and are unloaded from a second part of the chamber.
- the shape of the chamber and associated conveyer system can form a straight path or curved path.
- the processing chamber may be a carousel in which multiple substrates are moved about a central axis and are exposed to deposition, etch, annealing, cleaning, etc. processes throughout the carousel path.
- the substrate can be heated or cooled. Such heating or cooling can be accomplished by any suitable means including, but not limited to, changing the temperature of the substrate support and flowing heated or cooled gases to the substrate surface.
- the substrate support includes a heater/cooler which can be controlled to change the substrate temperature conductively.
- the gases either reactive gases or inert gases
- a heater/cooler is positioned within the chamber adjacent the substrate surface to convectively change the substrate temperature.
- the substrate can also be stationary or rotated during processing.
- a rotating substrate can be rotated continuously or in discreet steps.
- a substrate may be rotated throughout the entire process, or the substrate can be rotated by a small amount between exposures to different reactive or purge gases.
- Rotating the substrate during processing may help produce a more uniform deposition or etch by minimizing the effect of, for example, local variability in gas flow geometries.
- the substrate can be exposed to the first and second precursors either spatially or temporally separated processes.
- Temporal ALD is a traditional process in which the first precursor flows into the chamber to react with the surface. The first precursor is purged from the chamber before flowing the second precursor.
- spatial ALD both the first and second precursors are simultaneously flowed to the chamber but are separated spatially so that there is a region between the flows that prevents mixing of the precursors.
- spatial ALD the substrate is moved relative to the gas distribution plate, or vice-versa.
- the process may be a spatial ALD process.
- spatial ALD atomic layer deposition
- the reagents described above may not be compatible (i.e., result in reaction other than on the substrate surface and/or deposit on the chamber)
- spatial separation ensures that the reagents are not exposed to each in the gas phase.
- temporal ALD involves the purging the deposition chamber.
- spatial separation excess reagent does not need to be purged, and cross-contamination is limited.
- a lot of time can be used to purge a chamber, and therefore throughput can be increased by eliminating the purge step.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Plasma & Fusion (AREA)
- Chemical Vapour Deposition (AREA)
- General Physics & Mathematics (AREA)
Abstract
Description
Claims
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201680072606.3A CN108369896A (en) | 2015-12-10 | 2016-12-09 | It is annealed using the film in situ of space atomic layer deposition |
| KR1020187019610A KR102676605B1 (en) | 2015-12-10 | 2016-12-09 | In-situ film annealing using spatial atomic layer deposition |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562265982P | 2015-12-10 | 2015-12-10 | |
| US62/265,982 | 2015-12-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2017100630A1 true WO2017100630A1 (en) | 2017-06-15 |
Family
ID=59013625
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2016/065906 Ceased WO2017100630A1 (en) | 2015-12-10 | 2016-12-09 | In-situ film annealing with spatial atomic layer deposition |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US11515144B2 (en) |
| KR (1) | KR102676605B1 (en) |
| CN (1) | CN108369896A (en) |
| WO (1) | WO2017100630A1 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI833804B (en) * | 2018-09-21 | 2024-03-01 | 美商應用材料股份有限公司 | Gap-fill with aluminum-containing films |
| CN110184587B (en) * | 2019-05-23 | 2021-06-15 | 上海华力集成电路制造有限公司 | Method and chemical vapor deposition equipment for improving the uniformity of etching rate between silicon wafers |
| CN115985765B (en) * | 2023-01-03 | 2026-03-17 | 长鑫存储技术有限公司 | Film processing method, device and system |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040058293A1 (en) * | 2002-08-06 | 2004-03-25 | Tue Nguyen | Assembly line processing system |
| US20040248374A1 (en) * | 2003-06-03 | 2004-12-09 | International Business Machines Corporation | Filling high aspect ratio isolation structures with polysilazane based material |
| KR20070093914A (en) * | 2006-03-15 | 2007-09-19 | 에이에스엠지니텍코리아 주식회사 | Deposition apparatus and film deposition method using the same |
| JP2013055243A (en) * | 2011-09-05 | 2013-03-21 | Tokyo Electron Ltd | Deposition device, deposition method and storage medium |
| KR20130133622A (en) * | 2012-05-29 | 2013-12-09 | 주성엔지니어링(주) | Substrate processing apparatus and substrate processing method |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7625603B2 (en) * | 2003-11-14 | 2009-12-01 | Robert Bosch Gmbh | Crack and residue free conformal deposited silicon oxide with predictable and uniform etching characteristics |
| US7297608B1 (en) * | 2004-06-22 | 2007-11-20 | Novellus Systems, Inc. | Method for controlling properties of conformal silica nanolaminates formed by rapid vapor deposition |
| US7148155B1 (en) | 2004-10-26 | 2006-12-12 | Novellus Systems, Inc. | Sequential deposition/anneal film densification method |
| US7294583B1 (en) * | 2004-12-23 | 2007-11-13 | Novellus Systems, Inc. | Methods for the use of alkoxysilanol precursors for vapor deposition of SiO2 films |
| JP2006261434A (en) * | 2005-03-17 | 2006-09-28 | L'air Liquide Sa Pour L'etude & L'exploitation Des Procede S Georges Claude | Method for forming silicon oxide film |
| US7238586B2 (en) | 2005-07-21 | 2007-07-03 | United Microelectronics Corp. | Seamless trench fill method utilizing sub-atmospheric pressure chemical vapor deposition technique |
| US7767588B2 (en) | 2006-02-28 | 2010-08-03 | Freescale Semiconductor, Inc. | Method for forming a deposited oxide layer |
| CN101416296A (en) * | 2006-04-07 | 2009-04-22 | 应用材料股份有限公司 | Multi-step film hardening method for compacting film and improving gap filling effect |
| US7902080B2 (en) * | 2006-05-30 | 2011-03-08 | Applied Materials, Inc. | Deposition-plasma cure cycle process to enhance film quality of silicon dioxide |
| KR100905278B1 (en) * | 2007-07-19 | 2009-06-29 | 주식회사 아이피에스 | Thin film deposition apparatus, thin film deposition method and gap-fill method of semiconductor device |
| US7943531B2 (en) * | 2007-10-22 | 2011-05-17 | Applied Materials, Inc. | Methods for forming a silicon oxide layer over a substrate |
| US7858535B2 (en) * | 2008-05-02 | 2010-12-28 | Micron Technology, Inc. | Methods of reducing defect formation on silicon dioxide formed by atomic layer deposition (ALD) processes and methods of fabricating semiconductor structures |
| US20120177846A1 (en) * | 2011-01-07 | 2012-07-12 | Applied Materials, Inc. | Radical steam cvd |
| JP6011417B2 (en) * | 2012-06-15 | 2016-10-19 | 東京エレクトロン株式会社 | Film forming apparatus, substrate processing apparatus, and film forming method |
| KR102070400B1 (en) * | 2012-06-29 | 2020-01-28 | 주성엔지니어링(주) | Apparatus and method for processing substrate |
| US20140023794A1 (en) * | 2012-07-23 | 2014-01-23 | Maitreyee Mahajani | Method And Apparatus For Low Temperature ALD Deposition |
| US20140273530A1 (en) * | 2013-03-15 | 2014-09-18 | Victor Nguyen | Post-Deposition Treatment Methods For Silicon Nitride |
| US9401273B2 (en) * | 2013-12-11 | 2016-07-26 | Asm Ip Holding B.V. | Atomic layer deposition of silicon carbon nitride based materials |
| TWI643971B (en) * | 2014-01-05 | 2018-12-11 | 美商應用材料股份有限公司 | Film deposition using spatial atomic layer deposition or pulsed chemical vapor deposition |
| KR101840759B1 (en) * | 2014-01-05 | 2018-05-04 | 어플라이드 머티어리얼스, 인코포레이티드 | Film deposition using spatial atomic layer deposition or pulsed chemical vapor deposition |
-
2016
- 2016-12-09 US US15/374,438 patent/US11515144B2/en active Active
- 2016-12-09 CN CN201680072606.3A patent/CN108369896A/en active Pending
- 2016-12-09 WO PCT/US2016/065906 patent/WO2017100630A1/en not_active Ceased
- 2016-12-09 KR KR1020187019610A patent/KR102676605B1/en active Active
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040058293A1 (en) * | 2002-08-06 | 2004-03-25 | Tue Nguyen | Assembly line processing system |
| US20040248374A1 (en) * | 2003-06-03 | 2004-12-09 | International Business Machines Corporation | Filling high aspect ratio isolation structures with polysilazane based material |
| KR20070093914A (en) * | 2006-03-15 | 2007-09-19 | 에이에스엠지니텍코리아 주식회사 | Deposition apparatus and film deposition method using the same |
| JP2013055243A (en) * | 2011-09-05 | 2013-03-21 | Tokyo Electron Ltd | Deposition device, deposition method and storage medium |
| KR20130133622A (en) * | 2012-05-29 | 2013-12-09 | 주성엔지니어링(주) | Substrate processing apparatus and substrate processing method |
Also Published As
| Publication number | Publication date |
|---|---|
| US20170170009A1 (en) | 2017-06-15 |
| KR102676605B1 (en) | 2024-06-18 |
| KR20180083441A (en) | 2018-07-20 |
| US11515144B2 (en) | 2022-11-29 |
| CN108369896A (en) | 2018-08-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US11028477B2 (en) | Bottom-up gap-fill by surface poisoning treatment | |
| US10319583B2 (en) | Selective deposition of silicon nitride films for spacer applications | |
| US11702742B2 (en) | Methods of forming nucleation layers with halogenated silanes | |
| US10134581B2 (en) | Methods and apparatus for selective dry etch | |
| US20170053792A1 (en) | High Temperature Thermal ALD Silicon Nitride Films | |
| US20170306490A1 (en) | Enhanced Spatial ALD Of Metals Through Controlled Precursor Mixing | |
| US10147599B2 (en) | Methods for depositing low K and low wet etch rate dielectric thin films | |
| US20180312966A1 (en) | Methods For Spatial Metal Atomic Layer Deposition | |
| US12325910B2 (en) | Deposition of conformal and gap-fill amorphous silicon thin-films | |
| US12018363B2 (en) | Gap-fill with aluminum-containing films | |
| US11515144B2 (en) | In-situ film annealing with spatial atomic layer deposition | |
| US20160307748A1 (en) | Deposition Of Si-H Free Silicon Nitride | |
| US11015246B2 (en) | Apparatus and methods for depositing ALD films with enhanced chemical exchange |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 16873954 Country of ref document: EP Kind code of ref document: A1 |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| ENP | Entry into the national phase |
Ref document number: 20187019610 Country of ref document: KR Kind code of ref document: A |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 1020187019610 Country of ref document: KR |
|
| 122 | Ep: pct application non-entry in european phase |
Ref document number: 16873954 Country of ref document: EP Kind code of ref document: A1 |