WO2020198502A1 - Etch stop layer - Google Patents
Etch stop layer Download PDFInfo
- Publication number
- WO2020198502A1 WO2020198502A1 PCT/US2020/025004 US2020025004W WO2020198502A1 WO 2020198502 A1 WO2020198502 A1 WO 2020198502A1 US 2020025004 W US2020025004 W US 2020025004W WO 2020198502 A1 WO2020198502 A1 WO 2020198502A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- layer
- sin
- sub
- layers
- nitride
- 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
- H10P14/63—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]
-
- 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
- C23C16/345—Silicon nitride
-
- 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
- C23C16/505—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 using radio frequency discharges
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10B—ELECTRONIC MEMORY DEVICES
- H10B41/00—Electrically erasable-and-programmable ROM [EEPROM] devices comprising floating gates
- H10B41/20—Electrically erasable-and-programmable ROM [EEPROM] devices comprising floating gates characterised by three-dimensional [3D] arrangements, e.g. with cells on different height levels
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10B—ELECTRONIC MEMORY DEVICES
- H10B43/00—EEPROM devices comprising charge-trapping gate insulators
- H10B43/20—EEPROM devices comprising charge-trapping gate insulators characterised by three-dimensional [3D] arrangements, e.g. with cells on different height levels
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10B—ELECTRONIC MEMORY DEVICES
- H10B43/00—EEPROM devices comprising charge-trapping gate insulators
- H10B43/30—EEPROM devices comprising charge-trapping gate insulators characterised by the memory core region
- H10B43/35—EEPROM devices comprising charge-trapping gate insulators characterised by the memory core region with cell select transistors, e.g. NAND
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10B—ELECTRONIC MEMORY DEVICES
- H10B43/00—EEPROM devices comprising charge-trapping gate insulators
- H10B43/50—EEPROM devices comprising charge-trapping gate insulators characterised by the boundary region between the core and peripheral circuit regions
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10D—INORGANIC ELECTRIC SEMICONDUCTOR DEVICES
- H10D84/00—Integrated devices formed in or on semiconductor substrates that comprise only semiconducting layers, e.g. on Si wafers or on GaAs-on-Si wafers
- H10D84/80—Integrated devices formed in or on semiconductor substrates that comprise only semiconducting layers, e.g. on Si wafers or on GaAs-on-Si wafers characterised by the integration of at least one component covered by groups H10D12/00 or H10D30/00, e.g. integration of IGFETs
- H10D84/82—Integrated devices formed in or on semiconductor substrates that comprise only semiconducting layers, e.g. on Si wafers or on GaAs-on-Si wafers characterised by the integration of at least one component covered by groups H10D12/00 or H10D30/00, e.g. integration of IGFETs of only field-effect components
- H10D84/83—Integrated devices formed in or on semiconductor substrates that comprise only semiconducting layers, e.g. on Si wafers or on GaAs-on-Si wafers characterised by the integration of at least one component covered by groups H10D12/00 or H10D30/00, e.g. integration of IGFETs of only field-effect components of only insulated-gate FETs [IGFET]
-
- 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
- H10P14/662—Laminate layers, e.g. stacks of alternating high-k metal oxides
-
- 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
- H10P14/69—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
-
- 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
- H10P14/694—Inorganic materials composed of nitrides
- H10P14/6943—Inorganic materials composed of nitrides containing silicon
- H10P14/69433—Inorganic materials composed of nitrides containing silicon the material being a silicon nitride not containing oxygen, e.g. SixNy or SixByNz
-
- 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
- H10P50/00—Etching of wafers, substrates or parts of devices
- H10P50/20—Dry etching; Plasma etching; Reactive-ion etching
- H10P50/28—Dry etching; Plasma etching; Reactive-ion etching of insulating materials
- H10P50/282—Dry etching; Plasma etching; Reactive-ion etching of insulating materials of inorganic materials
- H10P50/283—Dry etching; Plasma etching; Reactive-ion etching of insulating materials of inorganic materials by chemical means
-
- 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
- H10P50/00—Etching of wafers, substrates or parts of devices
- H10P50/73—Etching of wafers, substrates or parts of devices using masks for insulating materials
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10B—ELECTRONIC MEMORY DEVICES
- H10B43/00—EEPROM devices comprising charge-trapping gate insulators
- H10B43/20—EEPROM devices comprising charge-trapping gate insulators characterised by three-dimensional [3D] arrangements, e.g. with cells on different height levels
- H10B43/23—EEPROM devices comprising charge-trapping gate insulators characterised by three-dimensional [3D] arrangements, e.g. with cells on different height levels with source and drain on different levels, e.g. with sloping channels
- H10B43/27—EEPROM devices comprising charge-trapping gate insulators characterised by three-dimensional [3D] arrangements, e.g. with cells on different height levels with source and drain on different levels, e.g. with sloping channels the channels comprising vertical portions, e.g. U-shaped channels
Definitions
- One aspect of the disclosure relates to a method including providing a substrate having alternating oxide layers and nitride layers arranged in a staircase pattern including exposed horizontal nitride surfaces and exposed oxide and nitride sidewall surfaces; depositing a silicon nitride (SiN) layer over the alternating oxide and nitride layers; and treating the SiN layer to selectively densify the SiN layer deposited on the exposed horizontal nitride surfaces.
- SiN silicon nitride
- the method further includes wet etching the treated SiN layer to form discrete SiN pads.
- a discrete SiN pad is at least 10 nm from the near sidewall surface.
- a discrete SiN pad is at least 10 nm thick.
- the method further includes replacing the SiN pads with tungsten landing pads.
- the deposition and treating operations are performed in the same chamber.
- depositing the SiN layer includes a plasma enhanced chemical vapor deposition (PECVD) process.
- PECVD plasma enhanced chemical vapor deposition
- treating the SiN layer includes exposing the substrate to a capacitively-coupled plasma. It may be generated from an inert gas.
- performing the depositing and treating operations includes performing multiple cycles of depositing a portion of the conformal SiN layer followed by treating the deposited portion.
- the conformal SiN layer includes multiple sub-layers, wherein at least two sub-layers have different wet etch rates (WERs).
- WERs wet etch rates
- one of the multiple sub-layers is an etch stop (ES) sub-layer having a lower WER than the other sub-layer or sub-layers of the multiple sub-layers.
- the ES layer has a WER of no more than 50 A/min in a wet etchant.
- one of the multiple sub-layers is a sub layer having a WER of at least 100 A/min in a wet etchant.
- the ES sub layer is disposed between two sub-layers each being thicker than the ES sub-layer and having a WER greater than the ES sub-layer.
- the ES sub-layer is the top layer of the SiN layer.
- the SiN film is deposited from silane (S1H4) and ammonia (Mb).
- the SiEL t and N3 ⁇ 4 are in a process gas that further includes nitrogen (N2).
- the method further includes replacing the nitride layers with tungsten wordlines.
- Another aspect of the disclosure relates to method including providing a substrate having horizontal and sidewall surfaces; depositing a silicon nitride (SiN) layer over the horizontal and sidewall surfaces; and treating the SiN layer to selectively densify the conformal SiN layer deposited on the horizontal surfaces.
- the method further includes wet etching the treated layer to form discrete SiN pads.
- Yet another aspect of the disclosure relates to a method including providing a substrate having horizontal and sidewall surfaces; performing one or more first cycles to form a first sub layer, each of the one or more first cycles including depositing an amount of SiN on the horizontal and sidewall surfaces by PECVD and exposing the deposited amount of SiN to a capacitively coupled plasma generated from an inert gas; performing one or more second cycles to form an etch stop sub-layer, each of the one or more second cycles including: depositing an amount of SiN on the first sub-layer by PECVD and exposing the deposited amount of SiN to an capacitively coupled plasma generated from an inert gas using low frequency radio frequency (LFRF) power.
- LFRF low frequency radio frequency
- the LFRF power in the one or more second cycles is greater than the LFRF power, if any, in the one or more first cycles.
- Another aspect of the disclosure relates to an apparatus including a PECVD deposition chamber including a LFRF plasma generator and a HFRF plasma generator; and a controller including instructions to perform any of the methods disclosed herein.
- Figure 1A is a process flow diagram depicting operations for a method according to certain embodiments.
- Figure IB is a process flow diagram depicting operations for a method of forming a 3-D NAND structure.
- Figures 2, 3, and 4A are schematic illustrations of a substrate in a patterning scheme.
- Figure 4B is a partial view of the substrate shown in Figure 4A.
- Figures 5A, 6A, 7A, 8, and 9 are schematic illustrations of a substrate in a patterning scheme.
- Figures 5B, 6B, and 7B are side views of schematic illustrations of substrates depicted in Figures 5A, 6A, and 7A, respectively.
- Figure 10 is a process flow diagram depicting operations for a method in accordance with certain embodiments.
- Figures 11-15 are schematic illustrations of a substrate in a patterning scheme.
- Figure 16 illustrates examples of various silicon nitride (SiN) stacks including sub-layers having different wet etch rates (WERs).
- Figure 17 illustrates target separation (S) and thickness (T) of a SiN pad according to certain embodiments.
- Figure 18 is a process flow diagram depicting operations for a method according to certain embodiments.
- Figure 19 is graph showing separation and remaining thickness vs etch time for SiN pads formed according to certain embodiments.
- Figure 20 is a schematic diagram of an example process chamber for performing certain disclosed embodiments.
- Figure 21 is a schematic diagram of an example process tool for performing certain disclosed embodiments.
- a material on a substrate such as a wafer, substrate, or other work piece.
- the work piece may be of various shapes, sizes, and materials.
- the terms“wafer” and“substrate,” are used interchangeably.
- VNAND vertical NAND
- existing techniques for forming 3D NAND structures are limited to vertical scaling: the number of memory layers are increased. To obtain the desired cost scaling per bit, it is critical to not increase the number of process steps in proportion to the layer increase.
- an oxide filler is deposited over alternating oxide and nitride layers that are arranged in a staircase pattern.
- the nitride layers are then replaced by a metal film, typically comprising tungsten to form the wordlines.
- Vias are then formed in the oxide filler.
- the vias extend vertically to contact the tungsten wordlines, which now form the treads of the staircase.
- Metal, such as tungsten is deposited in the vias to form interconnects which extend to and contact the tungsten wordlines.
- the staircase has more treads and becomes deeper. In addition, to reduce the overall height of the memory stack, it is desirable to thin the wordlines.
- the wordlines that form the staircase treads also fulfill the function of etch stop for the via etch. For cost reasons it is desirable to form the vias in one masking and etch step. However, as the staircase gets deeper and the wordlines get thinner, as demanded by scaling, it becomes increasingly difficult to have the upper wordlines survive the long overetch needed to reach the bottom wordlines. Thus, contact surfaces on wordlines located at higher positions on the staircase may be over-etched relative to wordlines located toward the bottom of the staircase pattern. As a result, the etch may punch through those wordlines to reach another wordline below. When the via is then filled with metal these wordlines will be shorted, causing yield loss.
- the methods involve deposition of a SiN layer over a staircase followed by a treatment to selectively densify the SiN layer on the horizontal surfaces with respect to the sidewall surfaces.
- a wet etch is then performed to remove SiN from the sidewall surfaces.
- the selective treatment results in significantly different wet etch rates (WERs) between the horizontal surfaces and the sidewalls. After the wet etch, the SiN layer remains on the horizontal surfaces and is removed from the sidewalls.
- FIG. 1 A shows a process flow diagram of operations performed in accordance with the methods described herein.
- operation 103 a layer of SiN is deposited over a structure having horizontal and vertical surfaces (also referred to as sidewall surfaces).
- operation 103 can involve plasma enhanced chemical vapor deposition (PECVD), plasma enhanced atomic layer deposition (PEALD), or thermal atomic layer deposition (ALD).
- PECVD plasma enhanced chemical vapor deposition
- PEALD plasma enhanced atomic layer deposition
- ALD thermal atomic layer deposition
- the total thickness deposited can depend on one or more of the following targets: 1) a remaining SiN thickness on the horizontal surfaces after wet etch (which determines tungsten landing pad thickness), 2) the minimum distance of SiN from the sidewalls of the staircase structure, and 3) lack of over-etch to achieve (1) and (2).
- the thickness may be between 300 A-900 A.
- the SiN film deposits on both the horizontal and vertical surfaces of the structure. It is generally conformal to the structure, though depending on the deposition method, there may be some variation in thickness on the sidewall vs horizontal surface thicknesses. It should be noted that the term“vertical” as used herein includes near 90° from planar as well as perfectly vertical surfaces. For example, a vertical surface may be +/- 10° or +/- 5° or +/- 1° or +/- 0.5 from 90°. Similarly, horizontal surfaces may vary +/- 5° or +/- l° or +/- 0.5 from 180°.
- PECVD can be used to provide relatively fast deposition.
- silane (S1H4) and ammonia (NH3) may be reacted in a PECVD deposition to form SiN.
- Nitrogen (N2) or an inert gas such as argon (Ar) or helium (He) may be used as a carrier gas.
- Other silicon- containing precursors may be used to deposit SiN including but not limited to organosilanes.
- other nitrogen containing gases such as N2 may be used as co-reactants as appropriate.
- the silicon nitride film is treated to selectively densify the horizontal surfaces.
- selectively densify refers to densifying the SiN film on the horizontal surfaces while the SiN film on the vertical surfaces is not densified or is densified to a significantly lesser extent.
- Operation 105 can involve exposing the deposited film to an inert gas plasma. For PECVD reactions or PEALD reactions, this may be performed in the deposition chamber.
- a bias voltage may be applied to the substrate to increase the directionality of the plasma, however, the method may be performed without a bias.
- a capacitively-coupled in-situ Ar plasma with no substrate bias for example has been demonstrated to selectively densify film on horizontal surfaces.
- operations 103 and 105 may be performed in multiple interspersed stages. That is, a first amount of a silicon nitride may be deposited then treated, a second amount of a silicon nitride film may be deposited then treated, etc. until the full thickness of SiN film is formed. This may be useful if the treatment has a limited penetration depth to ensure that the full thickness of film is treated.
- a wet etch is then performed to selectively remove the SiN film from the vertical surfaces in an operation 107.
- Dilute hydrofluoric acid (DHF) may be used, though other wet etchants such as phosphoric acid may be used.
- the SiN layer may have multiple sub-layers having different WERs.
- the method of Figure 1 A may be performed as part of a method of forming a 3D NAND structure.
- Figure IB shows a process flow diagram of operations performed in accordance with a method for forming a 3D NAND structure.
- a substrate is provided.
- the substrate is a semiconductor substrate.
- the substrate may be a silicon wafer, e.g., a 200-mm wafer, a 300-mm wafer, or a 450-mm wafer, including wafers having one or more layers of material, such as dielectric, conducting, or semi-conducting material deposited thereon.
- An example substrate 100 is provided as a schematic illustration in Figure 2.
- Mo molybdenum
- a film stack of alternating oxide and nitride films is deposited on the substrate.
- the oxide layer deposited is a silicon oxide layer.
- the nitride layer deposited is a silicon nitride layer.
- Each oxide and nitride layer may be deposited to about the same thickness, such as between about 10 nm and about 100 nm, for example about 25 nm to 35 nm in some embodiments.
- the oxide layers may be deposited at a deposition temperature of between about room temperature and about 700°C. It will be understood that“deposition temperature” (or“substrate temperature”) as used herein refers to the temperature that the pedestal holding the substrate is set to during deposition.
- Oxide and nitride layers for forming the alternating oxide and nitride film stack may be deposited using any suitable technique, such as ALD, PEALD, chemical vapor deposition (CVD), PECVD, or sputtering. In various embodiments, the oxide and nitride layers are deposited by PECVD.
- the film stack may include, for example, between 48 and 512 layers of alternating oxide and nitride layers with more alternating layers possible. Each oxide or nitride layer constitutes one layer.
- the film stack including the alternating oxide and nitride layers may be referred to as an oxide-nitride-oxide-nitride (ONON) stack.
- Figure 3 shows an example schematic illustration of a substrate 100 with alternating oxide 101 and nitride 102 films deposited on the substrate 100. Note that while the structure shown in Figure 3 shows an oxide deposited first, followed by nitride, oxide, nitride, etc., nitride may be deposited first, followed by oxide, nitride, oxide, etc.
- a staircase pattern is formed on the substrate.
- A“staircase pattern” as referred to herein describes two or more steps, each step including an oxide layer and a nitride layer. It will be understood that the top layer of each set of oxide and nitride layers may be either an oxide layer or a nitride layer for formation of steps in a staircase.
- the staircase pattern includes between 24 and 256 steps.
- the staircase pattern may be formed using a variety of patterning techniques. One technique includes depositing a sacrificial layer over the substrate and masking regions of the substrate to etch each set of oxide and nitride layers to form the staircase. Another technique include patterning photoresist, etching, trimming the resist, then repeating the etch and trim operations until the resist is too thin at which point it is reapplied.
- Figure 4A provides an example of a substrate 100 including a staircase pattern of oxide layers 111 and nitride layers 112 with a hardmask 110 over the topmost nitride layer.
- Figure 4A shows four steps of a staircase pattern, it will be understood that a staircase pattern may have any number of steps, such as between 24 and 256 steps.
- Each step includes a nitride layer and an oxide layer.
- the region of each step extending out from the edge of the step above it may be referred to as an“exposed” region of the step or topmost layer of the step, or portion suitable for deposition thereon. As shown, the exposed region is nitride.
- Oxide layers 111 are positioned parallel to, and in between, nitride layers 112. Each set of one oxide layer 111 followed by one nitride layer 112 is longer than the set immediately above it, thus forming the staircase pattern with exposed regions.
- oxide is deposited over the substrate.
- the oxide may be of the same or of different composition as the oxide deposited in layers of the ONON stack.
- the oxide deposited over the substrate is deposited at the same or a different deposition temperature than the deposition temperature used for depositing the oxide layers in the ONON stack.
- the deposition temperature may be between room temperature and about 600°C.
- Vertical slits may be subsequently etched into the substrate after depositing and planarizing the oxide.
- Figure 5A shows an example substrate 100 including the ONON staircase, hardmask 110, and oxide 122 deposited over the substrate.
- Figure 5B shows a side view of the substrate 100 after vertical slits 135 are etched and the hardmask 110 is removed.
- nitride is selectively etched relative to oxide on the substrate. Etching may be performed using a selective dry etch process, such as by exposing the substrate to any one or more of the following gases: chlorine (Ck), oxygen (O 2 ), nitrous oxide (N 2 O), tetrafluoromethane (CF 4 ), sulfur tetrafluoride (SF 4 ), carbon dioxide (CO 2 ), fluoromethane (CH 3 F), nitrogen trifluoride (NF 3 ), nitrogen (N 2 ), hydrogen (Ik), ammonia (NH 3 ), methane (CH 4 ), sulfur hexafluoride (SFe), argon (Ar), carbonyl sulfide (COS), carbon disulfide (CS 2 ), hydrogen sulfide (H 2 S), and nitric oxide (NO).
- gases chlorine (Ck), oxygen (O 2 ), nitrous oxide (N 2 O), tetrafluoromethane (CF 4 ), sulfur tetrafluor
- the operation 190 removes the nitride layers from the ONON stack such that etch species flow into vertical slits formed in the staircase pattern and selectively etches nitride.
- the selective etching involves etching a first material at a rate faster than etching a second material.
- selectively etching nitride relative to oxide means nitride is etched at a faster rate than etching of oxide.
- Nitride can also be selectively etched using a wet etch process, such as by exposing the substrate to phosphoric acid (H 3 PO 4 ), diluted hydrofluoric acid (“DHF”) or a mixture of these solutions.
- H 3 PO 4 phosphoric acid
- DHF diluted hydrofluoric acid
- selectively removing nitride poses a risk for degradation and removal of oxide material at various interfaces, such as at the oxide-oxide interface at the end of each staircase. This is described further below with respect to Figure 6A.
- Figure 6A shows an example schematic illustration of a substrate 100 with horizontal gaps 132 formed from etching the nitride layers 112. As shown in the enlarged view depicted in the circle at 170, a gap 134 may form at the oxide-oxide interface due to the etching species flowing into the gaps 132 and etching away at the oxide during the etching operation.
- Figure 6B shows a side view of a cross-section of the substrate whereby gaps 132 are formed from selectively etching nitride.
- tungsten is deposited into the gaps of the substrate to form tungsten wordlines.
- Tungsten may be deposited by any suitable technique, such as ALD, CVD, PEALD, and PECVD.
- ALD atomic layer deposition
- CVD chemical vapor deposition
- PEALD PEALD
- PECVD PECVD
- one or more additional layers may be deposited prior to depositing bulk tungsten.
- an alumina (AI2O3) layer may be deposited as a blocking oxide, followed by a titanium nitride (TiN) barrier layer, and a tungsten nucleation layer.
- TiN titanium nitride
- Figure 7A shows an example of a substrate 100 including deposited tungsten wordlines 140. However, due to the degradation of the oxide at the oxide-oxide interface as shown in the zoomed-in view at 170, tungsten fills in the gap at 141, thereby connecting two wordlines 140, which can cause a short.
- Figure 7B shows a schematic illustration of the substrate in 7A at a cross- section from a side view with tungsten 140 deposited in the gaps where nitride was located previously.
- the oxide is vertically etched to form vias.
- the oxide may be etched by dry etching using exposure to an etchant such as one or more of the following gases: O2, Ar, C4F6, C4F8, SF 6 , CHF3, and CF4.
- Figure 8 shows an example substrate 100 including the ONON stack in a staircase pattern whereby vias 137 are etched in the oxide 122.
- etching species flows into the vias (e.g., 137a) that are etched for the shallow parts of the oxide, to thus etch through the tungsten layer 136 and even etching through another oxide layer 138.
- such a phenomenon is typically undesirable and referred to as“punchthrough,” or“breakthrough,” to the layers positioned beneath the intended tungsten wordline contact point or layer.
- tungsten is deposited in the vias to form interconnects to the tungsten wordlines.
- tungsten fills the vias (see filled tungsten via 142) and causes a short as circled in 172 of Figure 9.
- Vias vary in depth and may have a depth between about 1 micron and about 14 microns, or more. Shallow vias are at the top and may have a depth of less than 100 nm. Deep vias may have a depth greater than 3.0 microns.
- the critical dimension of vias formed in the oxide may be between about 50 nm and about 500 nm. Vias may be etched using a dry etch process which may involve masking operations to pattern the oxide.
- Challenges in forming 3D NAND structures include punchthrough of tungsten wordlines when etching vias of different depths. Extensive etching techniques that use a variety of chemistries and patterning processes to mask regions of the substrate to etch vias of different depths can reduce throughput and reduce efficiency of fabrication processes.
- the methods involve depositing SiN on exposed horizontal portions of nitride layers of the staircase pattern to form SiN pads. Material deposited on exposed nitride and oxide sidewall surfaces etched by a wet etch process. The nitride layers of the staircase pattern, along with the SiN pads formed on each nitride layer, are etched selective to the oxide layers to form horizontal gaps and vacant regions corresponding to the locations of the SiN pads. Tungsten fills the horizontal gaps and vacant regions to form tungsten wordlines and landing pads on the wordlines. Each of the landing pads has a sufficient thickness to function as an etch stop layer or a protective barrier to prevent an interconnect from punching through the tungsten wordline.
- Figure 10 is a process flow diagram of operations for a method performed in accordance with some embodiments.
- the method shown in Figure 10 results in the formation of landing pads at operation 1014.
- the thickness of each of the landing pads provides ongoing protection against punchthrough of interconnects through wordlines that are also formed with the landing pads at operation 1014.
- operations 1002 and 1004 may be the same as, or similar to, operations 182 and 184 presented earlier in Figure IB, respectively.
- a staircase pattern is formed on the substrate. Operation 1006 may be the same as or similar to operation 186 of Figure IB as described above.
- SiN is selectively formed on exposed horizontal surfaces of the nitride layers, at each nitride layer, of the staircase pattern to form SiN pads.
- a method as described in Figure 1A may be used. Further examples of selective formation of SiN are described below.
- oxide also referred to as oxide filler
- oxide filler is deposited over the staircase pattern, including the SiN pads formed on the nitride layers at operation 1010.
- the nitride layers with SiN pads extending from each nitride layer are selectively etched relative to the oxide layers and oxide filler to create horizontal gaps between the oxide layers in the staircase pattern, similar to that shown in Figures 6 A and 6B.
- the horizontal gaps are later filled with tungsten at operation 1014 through a gap-fill operation to form tungsten wordlines and to replace the SiN pads with tungsten landing pads tungsten.
- the landing pads are formed on the wordlines as shown in Figure 14, e.g., landing pads 180 formed on wordlines 140.
- This operation may be performed using any technique or process condition as described above with respect to operation 192 of Figure IB.
- the vacant regions created from etching the SiN pads are filled with tungsten during operation 1018 during the formation of the tungsten wordlines to form landing pads on the tungsten wordlines.
- the oxide 122 is then etched to form vias in operation 1016.
- a via is etched vertically through the oxide, e.g. similar to that shown in Figure 8, to contact and end at a landing pad extending from a wordlines.
- multiple vias extend to each of the landing pads formed on the staircase pattern. Formation of longer vias to contact wordlines near the bottom of the staircase pattern may require a relatively longer etch duration compared to the time needed to form shorter vias to contact wordlines near the top of the staircase pattern. Accordingly, an extended etch duration to form long vias that extend to wordlines near the bottom of the staircase pattern may result in vias intended to contact wordlines at the top of the staircase pattern punching through such wordlines.
- the process shown in Figure 10 protects against such punchthrough of vias through wordlines by forming a landing pads on each wordline. Each landing pad provides additional material to prevent penetration prior to punching through the wordline upon which the landing pad is formed.
- tungsten is deposited into the vias to form interconnects that extend through the oxide filler to contact the landing pads.
- the landing pads also protect against punchthrough of interconnects through the wordlines as well at operation 1020.
- Operation 1008 of Figure 10 is further illustrated and described in connection with Figures 11-18.
- the operation 1008 involves a PECVD process.
- PECVD processes are distinct from high density plasma chemical vapor deposition (HDP CVD) processes.
- PECVD processes use capacitively coupled plasmas (CCPs);
- HDP CVD processes use inductively coupled plasmas.
- Inductively coupled HDP CVD process conditions and resulting films are different from capacitively-coupled PECVD processes.
- CCP processes the plasma is ignited between two electrodes.
- ICP processes the RF is applied at one end of a coil with the other end held at ground. Current flowing through the coil helps generate a plasma.
- Example frequencies for am HDP reactors are a plasma frequency of 400 kHz for coils and a frequency of 13.56 MHz for the pedestal where the wafer is placed.
- example frequencies may be up to 100 MHz, e.g., 13.56 MHz or 27 MHz, as applied to the either a showerhead or the pedestal electrodes.
- a low frequency RF e.g., 400 kHz
- RF power is pulsed in PECVD processes to improve step coverage.
- HDP reactors have a plasma density greater than 10 11 ions/cm 3 , higher than PECVD reactors. HDP typically have tighter ion energy distributions.
- a plasma frequency of 13.56 MHz is used to generate plasma as applied to.
- Ion energies in HDP reactors may be greater than in PECVD reactors.
- film composition and characteristics of films deposited in HDP CVD reactors are different than those deposited in PECVD reactors.
- SiN to be deposited to form SiN pads on exposed horizontal nitride surfaces may be formed by flowing a silicon-containing precursor and a nitrogen source into a PECVD chamber.
- Figure 11 shows an example of a conformal SiN layer 1120 deposited over a staircase structure.
- the staircase structure includes multiple pairs of oxide / nitride layers. The method may also be applied to staircase structures including single pair steps.
- Figure 12 shows the conformal SiN layer 1120 after treatment with sidewall SiN 1122 having a higher WER than the SiN horizontal surfaces.
- the SiN layer is conformal in that it deposits on both the horizonal and vertical surfaces of the structure.
- High step coverage e.g., the ratio of the sidewall thickness to the horizontal thickness
- a sidewall to horizontal thickness ratio is at least 0.7 (70% step coverage) or 0.8 (80% step coverage). If an ALD process is used, step coverage can be close or at 100%. For the PECVD processes described herein, step coverage of at least 70%-90% may be achieved.
- Figure 13 shows SiN pads 182 extending from each nitride layer 112. Each SiN pad 182 is spaced apart from the oxide sidewall surface 128 such that each pad SiN forms a notch on the end of its nitride layer 112.
- the nitride layers 112 and the SiN pads 182 deposited thereon, respectively, are etched relative to oxide on the substrate. Etching is conducted substantially as described for operation 190, as shown in Figure IB, to remove nitride layers 112 by flowing etchant species vertically through a slit in the ONON stack such that etchant species flow into the vertical slit and selectively etches nitride.
- Nitride may be selectively etched using a wet etch process, such as by exposing the substrate to phosphoric acid (H3PO4), or diluted hydrofluoric acid (“DHF”), or a mixture of these solutions.
- H3PO4 phosphoric acid
- DHF diluted hydrofluoric acid
- Figure 6A shows an example schematic illustration of a substrate 100 with horizontal gaps 132 formed from etching nitride.
- oxide 122 is vertically etched to form vias, later filled with tungsten to form interconnects 142, as shown in Figure 15.
- oxide 122 may be etched by dry etching conducted by exposure to any one or more of the following gases: O2, Ar, C4F6, C4F8, SF6, CHF3, and CF4.
- the depth of each landing pad 182 on each wordline 140 provides additional tungsten through which an interconnect 142 must penetrate prior to punching through to below wordlines 140, as shown in Figure 15. Accordingly, the possibility of a punchthrough condition is greatly minimized with usage of landing pads 182. Accordingly, the overall structural integrity of the ONON stack is preserved.
- the SiN layers may include two or more sub-layers.
- One of the sub-layers may have very low WER (e.g., no more than 30 A/min) and be referred to as an etch stop (ES) layer.
- Another sub-layer may have a higher etch rate (e.g. greater than 70 A/min, greater than 100 A/min, or greater than 120 A/min) for fast sidewall removal and separation.
- Figure 16 includes examples of different stacks of sub-layers. At 1610, a stack including sub-layers 1601, 1602, 1603, and 1604 is shown.
- Sub-layer 1602 is an ES layer, which has a lower WER than the sub-layers 1601, 1603, and 1604.
- the stack includes layers 1601, 1602, and 1603, with sub-layer 1602 being the ES layer.
- the ES layer is the top-most layer as shown at 1630 and 1640, with sub-layer 1601 being the ES layer.
- the ES layer could be the bottom layer, though it can be advantageous to have non-ES layers make up the bulk of the remaining SiN thickness as they are faster to form.
- the ES layer may represent a small amount of the overall thickness of the deposition SiN layer. For example, for about 600 A deposited, it may be only 40 A. Using such a sub-layer can allow higher WERs to be used for the other layers in the stack, allowing fast sidewall removal and separation from the sidewall.
- any two of the sub-layers 1601, 1602, 1603, and 1604 may have the same or different WER.
- Each sub-layer may also be characterized by its refractive index (RI) at 633 nm.
- RI refractive index
- Different WERs and/or RIs may be achieved by varying the treatment operation appropriately.
- Lower WERs can be achieved with one or more of longer treatment times and, for CCP treatment, the addition of low frequency (LF) power to generate the treatment plasma.
- Chamber pressure during treatment may also be lowered to lower WER.
- Deposition conditions may also be used to achieve a particular WER. For example, during PECVD deposition of SiN from SiFL and NH3, lowering temperature and lowering a N2 carrier gas flow can increase WER.
- the stack shown at 1610 may be:
- one or more of the sub-layers may be deposited without post-treatment for high WER.
- Differential etch rates may also be achieved by varying gas composition, RF frequency, showerhead-pedestal gap, and temperature.
- the WER of the SiN layer can depend on the following targets: 1) a remaining SiN thickness on the horizontal surfaces after wet etch (which determines tungsten landing pad thickness), 2) the minimum distance of SiN from the sidewalls of the staircase structure, and 3) lack of over-etch to achieve (1) and (2).
- Figure 17 shows an example of a SiN pad after deposition and treatment.
- the separation (S) and thickness (T) are labeled.
- S may range from 10 nm-60 nm
- T may range from 10-40 nm.
- Figure 18 shows an example of forming a SiN layer having a tri-layer structure including an ES layer sandwiched between two higher WER layers as shown at 1620.
- the method begins at 1802 by depositing a first portion of silicon nitride film.
- the first portion is generally thin enough such that it does not exceed the penetration depth of the subsequent treatment.
- Example thicknesses can range from 10A-50A, though it will be understood that the thickness depends on the particular treatment.
- deposition conditions can be varied to achieve particular WERs. Deposition conditions include substrate temperature, chamber pressure, reactant and carrier gas composition and flowrates, HF/LF power.
- example temperatures can range from 100°C-600°C; example pressures can range from 5 Torr - 20 Torr (relatively high for PECVD); example deposition chemistries are SiFE and N3 ⁇ 4 with Ar, N2, and/or He carrier gases.
- treatment conditions can include treatment time, chamber pressure HF/LF power, and treatment gas composition and flow rates.
- Example treatment times can range from 1-30 second, e.g, 5-20 seconds;
- example pressures can range from 1-20 torr, e.g, 3-10 Torr;
- example HF power can range from 500 W-1500 W;
- example LF power can be 0 in some cases or up 500 W;
- example treatment gases include Ar and He, with flow rates ranging from 1000-10000 seem each. It will be understood that the deposition and treatment conditions can fall outside the ranges described above. In some embodiments, there may be no post-deposition treatment time for this layer.
- operation 1804 may be performed without LF power to achieve a relatively high WER. This can facilitate the eventual etch of the SiN pad.
- Example treatment times may be 5-10 seconds, inclusive of the endpoint of the range.
- Operations 1802 and 1804 are repeated multiple times to form a bottom sub-layer. In an example, they may be repeated to deposit a sub-layer having between 100A-400A. If the amount deposited in operation 1802 is 20 A, this can be from 5-20 ti es.
- a portion of silicon nitride film is deposited.
- Deposition conditions may be as described above with respect to operation 1802.
- This portion is then treated at 1810 with second treatment conditions.
- the second treatment conditions are different from the first treatment conditions in that the values of one or more conditions are varied to change the WER.
- the operations 1808 and 1810 are forming part of the ES layer and to decrease the WER. In some embodiment, this involves one or both of adding (or raising) LF power and increasing treatment time. Treatment gas flowrates may be lowered and/or pressure may be lowered as well.
- Example treatment times may be from 15-25 seconds, inclusive.
- Operations 1808 and 1810 are repeated one or more times in operation 1812 to form a ES sub-layer. In an example, they may be repeated to deposit a sub-layer having between 20A-60A. Note that in this example, the ES layer is significantly thinner than the bottom sub-layer. In the full thickness is deposited in operation 1808, operation 1812 is omitted.
- a portion of silicon nitride film is then deposited at 1814.
- Deposition conditions may be as described above with respect to operation 1802.
- This portion is then treated at 1816 with third treatment conditions.
- the third treatment conditions are different from the second treatment conditions in that the values of one or more conditions are varied to change the WER, but may be the same or different as the first treatment conditions.
- the WER is relatively high to result in fast removal and separation from the sidewall.
- Example treatment times can range from 1-30 second, e.g, 5-20 seconds; example pressures can range from 1-20 torr, e.g, 3-10 Torr; example HF power can range from 500 W-1500 W; example LF power can be 0 in some cases or up 500 W; example treatment gases include Ar and He, with flowrates ranging from 1000-10000 seem each.
- Operations 1816 and 1818 are repeated multiple times to form a top sub-layer. In an example, they may be repeated to deposit a sub-layer having between 100A-400A.
- one or more of the sub-layers that are not ES layers may be deposited without a post deposition treatment.
- the sub-layer deposition may be performed in one step without cycling between deposition and treatment.
- the thickness of the one or more sub-layers under the ES layer is or near the target thickness.
- layer 1603 (at 1620 and 1630) or layers 1603 and 1604 (at 1610) may total 20 nm thickness or close to 20 nm.
- PECVD deposition conditions were varied to vary the WER in 100: 1 DHF. Post deposition treatments were held constant (10 seconds, 5.5 Torr, HF/LF 1000/0 watt, 10000 seem Ar/4000 seem He). For both deposition processes A and B, the chamber pressure was 9 Torr, HF/LF 575/0 watt with S1H4 and N3 ⁇ 4 process gasses.
- Process A used 550°C substrate temperature and 10000 seem Ar/6000 seem N2 carrier gas.
- Process B used 510°C substrate temperature and 10000 seem Ar/3000 seem N2/3OOO seem He carrier gas. (3000 seem He added to keep same total flow as Process A).
- WER for Process A was 90 A/min.
- WER for Process B was 141 A/min.
- the Process B PECVD deposition was used to form an ES layer. Treatment time was increased to 20 seconds (two lOand pressure was lowered to 4 Torr. HF/LF power was 800/300 watt (adding LF power). Gas flow rates were lowered 3000 seem Ar/2000 seem He. WER was 25 A/min.
- Figure 19 shows separation and remaining thickness vs etch time for a SiN stack that included an 20 ⁇ 10 A ES layer as described above sandwiched between layers formed as described for Process B. The results indicate that the ES layer holds the remaining thickness, with fast separation generated.
- a suitable apparatus for performing the disclosed methods typically includes hardware for accomplishing the process operations and a system controller having instructions for controlling process operations in accordance with the methods described above.
- FIG. 20 provides a block diagram of an example apparatus that may be used to practice the disclosed embodiments.
- a reactor 2000 includes a process chamber 2024, which encloses other components of the reactor and serves to contain the plasma generated by, e.g., a capacitor type system including a showerhead 2014 working in conjunction with a grounded heater block 2020.
- a high-frequency RF generator 2002 connected to a matching network 2006, and a low-frequency RF generator 2004 are connected to showerhead 2014.
- the power and frequency supplied by matching network 2006 is sufficient to generate a plasma from the process gas, for example 400-700W total energy.
- both the HFRF generator and the FFRF generator are used to treat an ES layer with the HFRF generator only used for PECVD deposition and treatment of the other layers.
- the high frequency RF component is generally between about 2-60MHz; and in particular embodiments, the HF component is about 13.56 MHz or 27 MHz.
- the low frequency EF component is generally between about 250-400 kHz; in a particular embodiment, the LF component is about 350 kHz.
- a pedestal 2018 supports a substrate 2016.
- the pedestal typically includes a chuck, a fork, or lift pins to hold and transfer the substrate during and between the deposition and/or plasma treatment reactions.
- the chuck may be an electrostatic chuck, a mechanical chuck or various other types of chuck as are available for use in the industry and/or research.
- the process gases are introduced via inlet 2012. Multiple source gas lines 2010 are connected to manifold 2008. The gases may be premixed or not. Appropriate valving and mass flow control mechanisms are employed to ensure that the correct gases are delivered during the deposition and plasma treatment phases of the process. In the case that the chemical precursor(s) are delivered in liquid form, liquid flow control mechanisms are employed. The liquid is then vaporized and mixed with other process gases during its transportation in a manifold heated above its vaporization point before reaching the deposition chamber.
- a vacuum pump 2026 e.g., a one or two stage mechanical dry pump and/or a turbomolecular pump draws process gases out and maintains a suitably low pressure within the reactor by a close loop controlled flow restriction device, such as a throttle valve or a pendulum valve.
- the methods may be implemented on a multi-station or single station tool.
- a VectorTM tool available from Lam Research of Fremont California having a multiple stations. It is possible to index the wafers after every deposition and/or post-deposition plasma treatment until all the depositions and treatments are completed, or multiple depositions and treatments can be conducted at a single station before indexing the wafer.
- reactor shown in Figure 20 is part of a tool for processing one or more wafers.
- An example of a tool including one or more reactors is provided in Figure 21.
- Figure 21 is a block diagram of a processing system suitable for conducting a deposition process in accordance with disclosed embodiments.
- the system 2100 includes a transfer module 2103, such as the wafer transfer system (WTS) used on the VectorTM platform available from Lam Research Corporation of Fremont, California.
- WTS wafer transfer system
- the transfer module 2103 provides a clean, pressurized environment to minimize the risk of contamination of workpieces, such as wafers, being processed as they are moved between the various processing stages.
- Chamber 2109 capable of performing a PECVD process.
- Chamber 2109 may include multiple stations 2111, 2113, 2115, and 2117 that may sequentially perform deposition or treatment operations.
- the system 2100 also includes one or more (in this case two) wafer source modules 2101 where wafers are stored before and after processing.
- a loadlock 2119 is located between the transfer module 2103 and the wafer source modules 2101.
- a device generally a robot arm unit
- Other modules 2105 and 2107 may be mounted on the transfer module. These may be deposition, etch, or treatment modules for example.
- Figure 21 also depicts an embodiment of a system controller 2150 employed to control process conditions and hardware states of process tool 2100.
- System controller 2150 may provide program instructions for implementing the above-described processes.
- the program instructions may control a variety of process parameters, such as RF power levels, pressure, temperature, flow rates, etc.
- a controller 2150 is part of a system, which may be part of the above-described examples.
- Such systems can include semiconductor processing equipment, including a processing tool or tools, chamber or chambers, a platform or platforms for processing, and/or specific processing components (a wafer pedestal, a gas flow system, etc.).
- These systems may be integrated with electronics for controlling their operation before, during, and after processing of a semiconductor wafer or substrate.
- the electronics may be referred to as the “controller,” which may control various components or subparts of the system or systems.
- the controller 2150 may be programmed to control any of the processes disclosed herein, including the delivery of processing gases, temperature settings (e.g., heating and/or cooling), pressure settings, vacuum settings, power settings, radio frequency (RF) generator settings, RF matching circuit settings, frequency settings, flow rate settings, fluid delivery settings, positional and operation settings, wafer transfers into and out of a tool and other transfer tools and/or load locks connected to or interfaced with a specific system.
- temperature settings e.g., heating and/or cooling
- RF radio frequency
- the controller 2150 may be defined as electronics having various integrated circuits, logic, memory, and/or software that receive instructions, issue instructions, control operation, enable cleaning operations, enable endpoint measurements, and the like.
- the integrated circuits may include chips in the form of firmware that store program instructions, digital signal processors (DSPs), chips defined as application specific integrated circuits (ASICs), and/or one or more microprocessors, or microcontrollers that execute program instructions (e.g., software).
- Program instructions may be instructions communicated to the controller in the form of various individual settings (or program files), defining operational parameters for carrying out a particular process on or for a semiconductor wafer or to a system.
- the operational parameters may, in some embodiments, be part of a recipe defined by process engineers to accomplish one or more processing steps during the fabrication of one or more layers, materials, metals, oxides, silicon, silicon dioxide, surfaces, circuits, and/or dies of a wafer.
- system controller 2150 controls all of the activities of process tool 2100.
- System controller 2150 may include one or more memory devices 2156, one or more mass storage devices 2154, and one or more processors 2152.
- Processor 2152 may include a CPU or computer, analog and/or digital input/output connections, stepper motor controller boards, etc.
- System controller 2150 executes system control software 2158 stored in mass storage device 2154, loaded into memory device 2156, and executed on processor 2152.
- the control logic may be hard coded in the controller 2150.
- Applications Specific Integrated Circuits, Programmable Logic Devices (e.g., field-programmable gate arrays, or FPGAs) and the like may be used for these purposes.
- System control software 2158 may include instructions for controlling the transfer of wafers into and out of a process chamber, timing of gases, mixture of gases, amount of gas flow, chamber and/or station pressure, backside gas flow pressure, chamber and/or reactor temperature, wafer temperature, bias power, target power levels, RF power levels, pedestal, chuck and/or susceptor position, and other parameters of a particular process performed by process tool 2100.
- System control software 2158 may be configured in any suitable way. For example, various process tool component subroutines or control objects may be written to control operation of the process tool components necessary to carry out various process tool processes.
- System control software 2158 may be coded in any suitable computer readable programming language.
- the controller 2150 may be a part of or coupled to a computer that is integrated with, coupled to the system, otherwise networked to the system, or a combination thereof.
- the controller 2150 may be in the“cloud” or all or a part of a fab host computer system, which can allow for remote access of the wafer processing.
- the computer may enable remote access to the system to monitor current progress of fabrication operations, examine a history of past fabrication operations, examine trends or performance metrics from a plurality of fabrication operations, to change parameters of current processing, to set processing steps to follow a current processing, or to start a new process.
- a remote computer e.g.
- a server can provide process recipes to a system over a network, which may include a local network or the Internet.
- the remote computer may include a user interface that enables entry or programming of parameters and/or settings, which are then communicated to the system from the remote computer.
- the controller 2150 receives instructions in the form of data, which specify parameters for each of the processing steps to be performed during one or more operations. It should be understood that the parameters may be specific to the type of process to be performed and the type of tool that the controller is configured to interface with or control.
- the controller 2150 may be distributed, such as by including one or more discrete controllers that are networked together and working towards a common purpose, such as the processes and controls described herein.
- An example of a distributed controller for such purposes would be one or more integrated circuits on a chamber in communication with one or more integrated circuits located remotely (such as at the platform level or as part of a remote computer) that combine to control a process on the chamber.
- system control software 2158 may include input/output control (IOC) sequencing instructions for controlling the various parameters described above.
- IOC input/output control
- Other computer software and/or programs stored on mass storage device 2154 and/or memory device 2156 associated with system controller 2150 may be employed in some embodiments. Examples of programs or sections of programs for this purpose include a wafer positioning program, a process gas control program, a pressure control program, a heater control program, and a plasma control program.
- a wafer positioning program may include program code for process tool components that are used to load a wafer onto a pedestal and to control the spacing between the wafer and other parts of process tool 2100.
- a process gas control program may include code for controlling gas composition (e.g., deposition gases, treatment gases, carrier gases, etc., as described herein) and flow rates and optionally for flowing gas into one or more process stations prior to deposition in order to stabilize the pressure in the process station.
- a pressure control program may include code for controlling the pressure in the process station by regulating, for example, a throttle valve in the exhaust system of the process station, a gas flow into the process station.
- a heater control program may include code for controlling the current to a heating unit that is used to heat the workpiece. Alternatively, the heater control program may control delivery of a heat transfer gas (such as helium) to the wafer.
- a plasma control program may include code for setting RF power levels applied to the process electrodes and, if appropriate, the bias in one or more process stations in accordance with the embodiments herein.
- a pressure control program may include code for maintaining the pressure in the reaction chamber in accordance with the embodiments herein.
- the user interface may include a display screen, graphical software displays of the apparatus and/or process conditions, and user input devices such as pointing devices, keyboards, touch screens, microphones, etc.
- parameters adjusted by system controller 2150 may relate to process conditions.
- process conditions include process gas composition and flow rates, temperature, pressure, plasma conditions (such as RF power levels), pressure, temperature, etc. These parameters may be provided to the user in the form of a recipe, which may be entered utilizing the user interface.
- Signals for monitoring the process may be provided by analog and/or digital input connections of system controller 2150 from various process tool sensors.
- the signals for controlling the process may be output on the analog and digital output connections of process tool 2100.
- process tool sensors that may be monitored include mass flow controllers, pressure sensors (such as manometers), thermocouples, etc. Appropriately programmed feedback and control algorithms may be used with data from these sensors to maintain process conditions.
- example systems may include a plasma etch chamber or module, a deposition chamber or module, a spin-rinse chamber or module, a metal plating chamber or module, a clean chamber or module, a bevel edge etch chamber or module, a physical vapor deposition (PVD) chamber or module, a chemical vapor deposition (CVD) chamber or module, an atomic layer deposition (ALD) chamber or module, an atomic layer etch (ALE) chamber or module, an ion implantation chamber or module, a track chamber or module, and any other semiconductor processing systems that may be associated or used in the fabrication and/or manufacturing of semiconductor wafers.
- PVD physical vapor deposition
- CVD chemical vapor deposition
- ALD atomic layer deposition
- ALE atomic layer etch
- the controller might communicate with one or more of other tool circuits or modules, other tool components, cluster tools, other tool interfaces, adjacent tools, neighboring tools, tools located throughout a factory, a main computer, another controller, or tools used in material transport that bring containers of wafers to and from tool locations and/or load ports in a semiconductor manufacturing factory.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Metallurgy (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Organic Chemistry (AREA)
- Plasma & Fusion (AREA)
- Physics & Mathematics (AREA)
- Inorganic Chemistry (AREA)
- Semiconductor Memories (AREA)
- Internal Circuitry In Semiconductor Integrated Circuit Devices (AREA)
- Non-Volatile Memory (AREA)
- Drying Of Semiconductors (AREA)
- Weting (AREA)
- Formation Of Insulating Films (AREA)
- Chemical Vapour Deposition (AREA)
Abstract
Description
Claims
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1020217035097A KR102952096B1 (en) | 2019-03-28 | 2020-03-26 | Etching stop layer |
| JP2021557622A JP2022527468A (en) | 2019-03-28 | 2020-03-26 | Etching stop layer |
| US17/598,830 US12087572B2 (en) | 2019-03-28 | 2020-03-26 | Etch stop layer |
| SG11202110691VA SG11202110691VA (en) | 2019-03-28 | 2020-03-26 | Etch stop layer |
| CN202080039328.8A CN113892168B (en) | 2019-03-28 | 2020-03-26 | Etch stop layer |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201962825632P | 2019-03-28 | 2019-03-28 | |
| US62/825,632 | 2019-03-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2020198502A1 true WO2020198502A1 (en) | 2020-10-01 |
Family
ID=72608483
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2020/025004 Ceased WO2020198502A1 (en) | 2019-03-28 | 2020-03-26 | Etch stop layer |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US12087572B2 (en) |
| JP (1) | JP2022527468A (en) |
| KR (1) | KR102952096B1 (en) |
| CN (1) | CN113892168B (en) |
| SG (1) | SG11202110691VA (en) |
| TW (1) | TWI886122B (en) |
| WO (1) | WO2020198502A1 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2021168637A1 (en) * | 2020-02-25 | 2021-09-02 | Yangtze Memory Technologies Co., Ltd. | 3d nand memory device and method of forming the same |
| US11978625B2 (en) * | 2021-10-18 | 2024-05-07 | Applied Materials, Inc. | Methods of forming metal nitride films |
| KR20240032448A (en) | 2022-09-02 | 2024-03-12 | 삼성전자주식회사 | Methods of semiconductor devices |
| US12512329B2 (en) * | 2023-04-06 | 2025-12-30 | Tokyo Electron Limited | Multi level contact etch |
| US12520474B2 (en) * | 2023-05-11 | 2026-01-06 | Nanya Technology Corporation | Semiconductor device including buried word line |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20160148949A1 (en) * | 2013-08-12 | 2016-05-26 | Micron Technology, Inc. | Semiconductor structures including dielectric materials having differing removal rates |
| US20160329238A1 (en) * | 2014-02-26 | 2016-11-10 | Lam Research Corporation | Inhibitor plasma mediated atomic layer deposition for seamless feature fill |
| US20170062469A1 (en) * | 2015-08-27 | 2017-03-02 | Applied Materials, Inc. | Vnand tensile thick teos oxide |
| US20180323057A1 (en) * | 2016-07-01 | 2018-11-08 | Lam Research Corporation | Selective atomic layer deposition with post-dose treatment |
| US20190035810A1 (en) * | 2016-11-07 | 2019-01-31 | Asm Ip Holding B.V. | Method of processing a substrate and a device manufactured by using the method |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4376715B2 (en) | 2004-07-16 | 2009-12-02 | 三洋電機株式会社 | Manufacturing method of semiconductor device |
| WO2008153674A1 (en) | 2007-06-09 | 2008-12-18 | Boris Kobrin | Method and apparatus for anisotropic etching |
| US20110207323A1 (en) | 2010-02-25 | 2011-08-25 | Robert Ditizio | Method of forming and patterning conformal insulation layer in vias and etched structures |
| SE537101C2 (en) * | 2010-03-30 | 2015-01-07 | Fairchild Semiconductor | Semiconductor Component and Method for Designing a Structure in a Target Substrate for Manufacturing a Semiconductor Component |
| US8993460B2 (en) * | 2013-01-10 | 2015-03-31 | Novellus Systems, Inc. | Apparatuses and methods for depositing SiC/SiCN films via cross-metathesis reactions with organometallic co-reactants |
| US9257274B2 (en) | 2010-04-15 | 2016-02-09 | Lam Research Corporation | Gapfill of variable aspect ratio features with a composite PEALD and PECVD method |
| US8524612B2 (en) | 2010-09-23 | 2013-09-03 | Novellus Systems, Inc. | Plasma-activated deposition of conformal films |
| JP2012079762A (en) | 2010-09-30 | 2012-04-19 | Mitsubishi Heavy Ind Ltd | Insulation film forming apparatus and formation method |
| CN102479719B (en) * | 2010-11-30 | 2014-09-03 | 中芯国际集成电路制造(北京)有限公司 | Manufacturing method and stress layer structure of semiconductor device with strain memory function |
| US8809169B2 (en) | 2011-09-30 | 2014-08-19 | Tokyo Electron Limited | Multi-layer pattern for alternate ALD processes |
| FR3020718B1 (en) * | 2014-05-02 | 2016-06-03 | Ecole Polytech | METHOD AND SYSTEM FOR CONTROLLING ION FLOWS IN RF PLASMA |
| US9214333B1 (en) * | 2014-09-24 | 2015-12-15 | Lam Research Corporation | Methods and apparatuses for uniform reduction of the in-feature wet etch rate of a silicon nitride film formed by ALD |
| US9576811B2 (en) | 2015-01-12 | 2017-02-21 | Lam Research Corporation | Integrating atomic scale processes: ALD (atomic layer deposition) and ALE (atomic layer etch) |
| US10410857B2 (en) | 2015-08-24 | 2019-09-10 | Asm Ip Holding B.V. | Formation of SiN thin films |
| US10115601B2 (en) | 2016-02-03 | 2018-10-30 | Tokyo Electron Limited | Selective film formation for raised and recessed features using deposition and etching processes |
| US10529554B2 (en) | 2016-02-19 | 2020-01-07 | Asm Ip Holding B.V. | Method for forming silicon nitride film selectively on sidewalls or flat surfaces of trenches |
| US10468251B2 (en) | 2016-02-19 | 2019-11-05 | Asm Ip Holding B.V. | Method for forming spacers using silicon nitride film for spacer-defined multiple patterning |
| JP6946320B2 (en) * | 2016-03-13 | 2021-10-06 | アプライド マテリアルズ インコーポレイテッドApplied Materials,Incorporated | Selective deposition of silicon nitride film for spacers |
| TWI766014B (en) | 2017-05-11 | 2022-06-01 | 荷蘭商Asm智慧財產控股公司 | Method for forming silicon nitride film selectively on sidewalls or flat surfaces of trenches |
| CN110998790B (en) | 2017-08-04 | 2024-07-09 | 朗姆研究公司 | Selective SiN deposition on horizontal surfaces |
| US10763108B2 (en) | 2017-08-18 | 2020-09-01 | Lam Research Corporation | Geometrically selective deposition of a dielectric film |
| KR102443047B1 (en) * | 2017-11-16 | 2022-09-14 | 에이에스엠 아이피 홀딩 비.브이. | Substrate processing apparatus method and apparatus manufactured thereby |
| KR102190532B1 (en) * | 2017-11-22 | 2020-12-15 | (주)디엔에프 | Composition for silicon-containing thin films and method for producing silicon-containing thin film |
-
2020
- 2020-03-26 KR KR1020217035097A patent/KR102952096B1/en active Active
- 2020-03-26 JP JP2021557622A patent/JP2022527468A/en active Pending
- 2020-03-26 CN CN202080039328.8A patent/CN113892168B/en active Active
- 2020-03-26 US US17/598,830 patent/US12087572B2/en active Active
- 2020-03-26 SG SG11202110691VA patent/SG11202110691VA/en unknown
- 2020-03-26 WO PCT/US2020/025004 patent/WO2020198502A1/en not_active Ceased
- 2020-03-27 TW TW109110451A patent/TWI886122B/en active
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20160148949A1 (en) * | 2013-08-12 | 2016-05-26 | Micron Technology, Inc. | Semiconductor structures including dielectric materials having differing removal rates |
| US20160329238A1 (en) * | 2014-02-26 | 2016-11-10 | Lam Research Corporation | Inhibitor plasma mediated atomic layer deposition for seamless feature fill |
| US20170062469A1 (en) * | 2015-08-27 | 2017-03-02 | Applied Materials, Inc. | Vnand tensile thick teos oxide |
| US20180323057A1 (en) * | 2016-07-01 | 2018-11-08 | Lam Research Corporation | Selective atomic layer deposition with post-dose treatment |
| US20190035810A1 (en) * | 2016-11-07 | 2019-01-31 | Asm Ip Holding B.V. | Method of processing a substrate and a device manufactured by using the method |
Also Published As
| Publication number | Publication date |
|---|---|
| SG11202110691VA (en) | 2021-10-28 |
| CN113892168A (en) | 2022-01-04 |
| CN113892168B (en) | 2025-09-30 |
| KR102952096B1 (en) | 2026-04-13 |
| US20220181141A1 (en) | 2022-06-09 |
| TWI886122B (en) | 2025-06-11 |
| KR20210134431A (en) | 2021-11-09 |
| TW202105490A (en) | 2021-02-01 |
| US12087572B2 (en) | 2024-09-10 |
| JP2022527468A (en) | 2022-06-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR102675485B1 (en) | Selective deposition of SiN on horizontal surfaces | |
| US11670516B2 (en) | Metal-containing passivation for high aspect ratio etch | |
| KR102834037B1 (en) | Directional deposition in the etching chamber | |
| US20230298896A1 (en) | Metal-based liner protection for high aspect ratio plasma etch | |
| KR102653066B1 (en) | Removal of metal-doped carbon-based hardmask during semiconductor manufacturing | |
| US12087572B2 (en) | Etch stop layer | |
| KR20220149611A (en) | Atomic Layer Etching of Molybdenum | |
| US20230035732A1 (en) | Efficient cleaning and etching of high aspect ratio structures | |
| US12237175B2 (en) | Polymerization protective liner for reactive ion etch in patterning | |
| WO2020028119A1 (en) | Non-selective and selective etching through alternating layers of materials | |
| KR20250043458A (en) | High aspect ratio carbon etching using a simulated Bosch process | |
| WO2025136832A1 (en) | Selective carbon removal treatment process using metastable activated radical species | |
| WO2026084990A1 (en) | Etching through silicon vias having different sizes with minimum depth loading |
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: 20779393 Country of ref document: EP Kind code of ref document: A1 |
|
| ENP | Entry into the national phase |
Ref document number: 2021557622 Country of ref document: JP Kind code of ref document: A |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| ENP | Entry into the national phase |
Ref document number: 20217035097 Country of ref document: KR Kind code of ref document: A |
|
| 122 | Ep: pct application non-entry in european phase |
Ref document number: 20779393 Country of ref document: EP Kind code of ref document: A1 |
|
| WWG | Wipo information: grant in national office |
Ref document number: 202080039328.8 Country of ref document: CN |