1. Field of Invention
The invention relates to a method for etching a feature in an anti-reflective coating (ARC) layer on a substrate, and more particularly to a method for etching a feature in a silicon-containing ARC layer.
2. Description of Related Art
Typically, during fabrication of integrated circuits (ICs), semiconductor production equipment utilize a (dry) plasma etch process to remove or etch material along fine lines or within vias or contacts patterned on a semiconductor substrate. The success of the plasma etching process requires that the etch chemistry includes chemical reactants suitable for selectively etching one material while substantially not etching another material. For example, on a semiconductor substrate, a pattern formed in a protective layer can be transferred to an underlying layer of a selected material utilizing a plasma etching process. The protective layer can comprise a radiation-sensitive layer, such as a photo-resist layer, having a pattern formed therein using a lithographic process. The protective layer can also comprise an anti-reflective coating (ARC) layer underlying the resist layer, wherein the pattern formed in the resist layer is transferred to the underlying ARC layer. In order to pattern smaller features than what is currently possible with standard lithographic techniques, it is desirable to reduce the critical dimension (CD) of the pattern during the transfer of the pattern from the resist layer to the ARC layer. Furthermore, it is desirable to correct for pattern deficiencies in the resist layer, such as edge roughness, during the transfer of the pattern from the resist layer to the ARC layer.
The invention relates to a method for etching a feature in a substrate.
Additionally, the invention relates to a method for etching a feature in an anti-reflective coating (ARC) layer on a substrate, and more particularly to a method for etching a feature in a silicon-containing ARC layer.
According to one embodiment, a method of dry developing an anti-reflective coating (ARC) layer on a substrate is described. The method comprises disposing a substrate comprising a multi-layer mask in a plasma processing system, wherein the multi-layer mask comprises a lithographic layer overlying a silicon-containing ARC layer and wherein the lithographic layer comprises a feature pattern formed therein using a lithographic process. A process recipe is established that is configured to cause a reduction of a first critical dimension (CD) of the feature pattern in the lithographic layer to a second CD of the feature pattern in the silicon-containing ARC layer. The method further comprises: introducing a process gas to the plasma processing system according to the process recipe, the process gas comprising a nitrogen-containing gas, a hydrogen-containing gas, and a CxHyFz-containing gas, wherein x, y, and z are integers greater than or equal to unity; forming plasma from the process gas in the plasma processing system according to the process recipe; and exposing the substrate to the plasma in order to transfer the feature pattern in the lithographic layer to the underlying silicon-containing ARC layer.
According to another embodiment, a method of dry developing a multi-layer mask on a substrate is described. The method comprises: forming the multi-layer mask on the substrate, wherein the multi-layer mask comprises a lithographic layer overlying a silicon-containing ARC layer which is overlying an organic dielectric layer (ODL); forming a feature pattern in the lithographic layer using a lithographic process; transferring the feature pattern from the lithographic layer to the silicon-containing ARC layer using a first dry plasma etching process, wherein the first dry plasma etching process comprises introducing a process gas having N2, H2, and CH2F2, forming plasma from the process gas, and exposing the substrate to the plasma; transferring the feature pattern from the silicon-containing ARC layer to the ODL using a second dry plasma etching process, wherein the second dry plasma etching process comprises introducing a second process gas having N2 and H2, forming a second plasma from the second process gas, and exposing the substrate to the second plasma; and reducing a first critical dimension (CD) of the feature pattern in the lithographic layer to a second CD of the feature pattern in the silicon-containing ARC layer.
In the accompanying drawings:
In the following description, for purposes of explanation and not limitation, specific details are set forth, such as a particular geometry of a processing system, descriptions of various components and processes used therein. However, it should be understood that the invention may be practiced in other embodiments that depart from these specific details.
Reference throughout this specification to “one embodiment” or “an embodiment” means that a particular feature, structure, material, or characteristic described in connection with the embodiment is included in at least one embodiment of the invention, but do not denote that they are present in every embodiment. Thus, the appearances of the phrases “in one embodiment” or “in an embodiment” in various places throughout this specification are not necessarily referring to the same embodiment of the invention. Furthermore, the particular features, structures, materials, or characteristics may be combined in any suitable manner in one or more embodiments. Various additional layers and/or structures may be included and/or described features may be omitted in other embodiments.
In material processing methodologies, plasma is often utilized to create and assist surface chemistry on a substrate to facilitate the removal of material from the substrate or to facilitate film forming reactions for depositing material on the substrate. During the etching of a substrate, plasma may be utilized to create reactive chemical species that are suitable for reacting with the certain materials on the surface of a substrate. Furthermore, during the etching of a substrate, plasma may be utilized to create charged species that are useful for delivering energy to surface reactions on the substrate.
According to one example, pattern etching comprises the application of a lithographic layer, such as a thin layer of radiation-sensitive material (e.g., photo-resist), to an upper surface of a substrate that is subsequently patterned in order to provide a mask for transferring this pattern to the underlying thin film on the substrate during etching. The patterning of the radiation-sensitive material generally involves exposure of the lithographic layer to a geometric pattern of electromagnetic (EM) radiation using, for example, a micro-lithography system, followed by the removal of the irradiated regions of the radiation-sensitive material (as in the case of positive photo-resist), or non-irradiated regions (as in the case of negative resist) using a developing solvent.
In order to pattern thinner features in the lithographic layer using conventional lithography techniques, multi-layer masks can be implemented. For example, the multi-layer mask may include a bilayer mask or trilayer mask. With the inclusion of a second or third layer, the uppermost lithographic layer may be thinner than the thickness customarily chosen to withstand the subsequent dry etching process(es) and, therefore, using conventional lithography techniques, finer features may be formed in the thinner lithographic layer. Thereafter, the finer feature formed in the lithographic layer may be transferred to the underlying second or third layers using a dry development process, such as a dry etching process. However, there still exists a need to produce even finer features in the multi-layer mask.
Furthermore, during pattern transfer, undulations or variations in the edge profile of the pattern as well as variations in pattern dimension, can be propagated into the underlying layers, such as the second mask layer in a multi-layer mask. These undulations may be referred to as edge roughness or line edge roughness (LER). Edge roughness may arise from damage to the layer of radiation-sensitive material. During the application of the radiation-sensitive material, the post-application bake (PAB), the exposure step, the post-exposure bake (PEB), or the wet developing step, or any combination thereof, the radiation-sensitive material may be damaged. Furthermore, damage may occur during the initial phases of the ARC layer etch or thin film etch. During pattern transfer, conventional process chemistries fail to mitigate damage to patterns due to roughness effects.
Moreover, during pattern transfer, there exists a need to produce features in the multi-layer mask, wherein the critical dimension (CD) is uniformly maintained or reduced across the substrate. For example, it is desirable to produce a uniform distribution of the CD bias (i.e., the difference between the initial CD in the lithographic layer and the final CD in the underlying second or third layer) across the substrate (e.g., center to edge). Furthermore, during pattern transfer, there still exists a need to produce features in the multi-layer mask, wherein an offset between the CD bias for nested (closely spaced) structures and the CD bias for isolated (widely spaced structures) is minimized.
Hence, there still exists a need to correct for pattern deficiencies in the multi-layer mask, such as CD bias and CD bias offset (between nested and isolated structures). During pattern transfer, conventional process chemistries fail to reduce the CD bias and the CD bias offset.
Therefore, according to an embodiment, a method of etching a feature in a substrate is schematically illustrated in
The substrate 100 may comprise a semiconductor substrate, a wafer, a flat panel display or a liquid crystal display.
The thin film 110 may comprise a conductive layer, a non-conductive layer, or a semi-conductive layer. For instance, the thin film 110 may include a material layer comprising a metal, metal oxide, metal nitride, metal oxynitride, metal silicate, metal silicide, silicon, poly-crystalline silicon (polysilicon), doped silicon, silicon dioxide, silicon nitride, silicon carbide, or silicon oxynitride, etc. Additionally, for instance, the thin film 110 may comprise a low dielectric constant (i.e., low-k) or ultra-low dielectric constant (i.e., ultra-low-k) dielectric layer having a nominal dielectric constant value less than the dielectric constant of SiO2, which is approximately 4 (e.g., the dielectric constant for thermal silicon dioxide can range from 3.8 to 3.9). More specifically, the thin film 110 may have a dielectric constant of less than 3.7, or a dielectric constant ranging from 1.6 to 3.7.
These dielectric layers may include at least one of an organic, inorganic, or inorganic-organic hybrid material. Additionally, these dielectric layers may be porous or non-porous.
For example, these dielectric layers may include an inorganic, silicate-based material, such as carbon doped silicon oxide (or organo siloxane), deposited using CVD techniques. Examples of such films include Black Diamond® CVD organosilicate glass (OSG) films commercially available from Applied Materials, Inc., or Coral® CVD films commercially available from Novellus Systems, Inc.
Alternatively, these dielectric layers may include porous inorganic-organic hybrid films comprised of a single-phase, such as a silicon oxide-based matrix having CH3 bonds that hinder full densification of the film during a curing or deposition process to create small voids (or pores). Still alternatively, these dielectric layers may include porous inorganic-organic hybrid films comprised of at least two phases, such as a carbon-doped silicon oxide-based matrix having pores of organic material (e.g., porogen) that is decomposed and evaporated during a curing process.
Still alternatively, these dielectric layers may include an inorganic, silicate-based material, such as hydrogen silsesquioxane (HSQ) or methyl silsesquioxane (MSQ), deposited using SOD (spin-on dielectric) techniques. Examples of such films include FOx® HSQ commercially available from Dow Corning, XLK porous HSQ commercially available from Dow Corning, and JSR LKD-5109 commercially available from JSR Microelectronics.
Still alternatively, these dielectric layers can comprise an organic material deposited using SOD techniques. Examples of such films include SiLK-I, SiLK-J, SiLK-H, SiLK-D, and porous SiLK® semiconductor dielectric resins commercially available from Dow Chemical, and GX-3™, and GX-3P™ semiconductor dielectric resins commercially available from Honeywell.
The thin film 110 can be formed using a vapor deposition technique, such as chemical vapor deposition (CVD), plasma enhanced CVD (PECVD), atomic layer deposition (ALD), plasma enhanced ALD (PEALD), physical vapor deposition (PVD), or ionized PVD (iPVD), or a spin-on technique, such as those offered in the Clean Track ACT 8 SOD (spin-on dielectric), ACT 12 SOD, and Lithius coating systems commercially available from Tokyo Electron Limited (TEL). The Clean Track ACT 8 (200 mm), ACT 12 (300 mm), and Lithius (300 mm) coating systems provide coat, bake, and cure tools for SOD materials. The track system can be configured for processing substrate sizes of 100 mm, 200 mm, 300 mm, and greater. Other systems and methods for forming a thin film on a substrate are well known to those skilled in the art of both spin-on technology and vapor deposition technology.
The lithographic layer 126 may comprise a layer of radiation-sensitive material, such as photo-resist. The photo-resist layer may comprise 248 nm (nanometer) resists, 193 nm resists, 157 nm resists, EUV (extreme ultraviolet) resists, or electron beam sensitive resist. The photo-resist layer can be formed using a track system. For example, the track system can comprise a Clean Track ACT 8, ACT 12, or Lithius resist coating and developing system commercially available from Tokyo Electron Limited (TEL). Other systems and methods for forming a photo-resist layer on a substrate are well known to those skilled in the art of spin-on resist technology.
The second mask layer 124 can comprise a silicon-containing layer, such as a silicon-containing anti-reflective coating (ARC) layer. For example, the second mask layer 124 may comprise a silicon-containing ARC having a silicon content of about 43% by weight or less. Additionally, for example, the second mask layer 124 may comprise a silicon-containing ARC having a silicon content of about 30% by weight or less. Additionally, for example, the second mask layer 124 may comprise a silicon-containing ARC having a silicon content of about 20% by weight or less. Additionally yet, for example, the second mask layer 124 may comprise a silicon-containing ARC having a silicon content of about 17% by weight. Furthermore, for example, the second mask layer 124 may comprise a silicon-containing ARC commercially available as Sepr-Shb Aseries SiARC from Shin Etsu Chemical Co., Ltd. The second mask layer 124 may, for example, be applied using spin coating technology, or a vapor deposition process.
The optional third mask layer 122 may comprise an inorganic layer or an organic layer. For example, the optional third mask layer 122 may comprise an organic dielectric layer (ODL). The ODL can include a photo-sensitive organic polymer or an etch type organic compound. For instance, the photo-sensitive organic polymer may be polyacrylate resin, epoxy resin, phenol resin, polyamide resin, polyimide resin, unsaturated polyester resin, polyphenylenether resin, polyphenylenesulfide resin, or benzocyclobutene (BCB). These materials may be formed using spin-on techniques. The lithographic layer 126 is imaged with an image pattern of EM radiation. The exposure to EM radiation through a reticle is performed in a dry or wet photo-lithography system. The image pattern can be formed using any suitable conventional stepping lithographic system, or scanning lithographic system. For example, the photo-lithographic system may be commercially available from ASML Netherlands B.V. (De Run 6501, 5504 DR Veldhoven, The Netherlands), or Canon USA, Inc., Semiconductor Equipment Division (3300 North First Street, San Jose, Calif. 95134). Thereafter, the image pattern is developed to form feature pattern 130 in the lithographic layer 126 having a first critical dimension (CD) 132. The developing process can include exposing the substrate to a developing solvent in a developing system, such as a track system. For example, the track system can comprise a Clean Track ACT 8, ACT 12, or Lithius resist coating and developing system commercially available from Tokyo Electron Limited (TEL).
As shown in
Thereafter, the method further comprises: in 530, introducing a process gas to the plasma processing system according to the process recipe, the process gas comprising a nitrogen-containing gas, a hydrogen-containing gas, and a CxHyFz-containing gas, wherein x, y, and z are integers greater than or equal to unity; in 540, forming plasma from the process gas in the plasma processing system according to the process recipe; and, in 550, exposing the substrate to the plasma in order to transfer the feature pattern 130 in the lithographic layer 126 to the underlying second mask layer 124 which may contain a silicon-containing ARC layer.
The nitrogen-containing gas may comprise N2, NH3, NO, NO2, or N2O, or any combination of two or more thereof. The hydrogen-containing gas may comprise H2, or NH3, or both H2 and NH3. The CxFyHz-containing gas may include any gas containing carbon (C), fluorine (F), and hydrogen (H) (e.g., a hydrofluorocarbon gas). For example, the hydrofluorocarbon gas may include introducing trifluoromethane (CHF3), or difluoromethane (CH2F2), or both CHF3 and CH2F2.
The process gas can further comprise an inert gas. Alternatively, the process gas can comprise a noble gas. Alternatively yet, the process gas can comprise argon (Ar).
In one example, the process gas comprises N2 and H2. In another example, the process gas comprises NH3. In another embodiment, the process gas comprises or consists essentially of N2, H2, and CH2F2. In yet another embodiment, the process gas comprises or consists essentially of NH3 and CH2F2.
The process recipe may further comprise: setting a flow rate of one or more constituents of the process gas; setting a pressure in the plasma processing system; setting a first power level for a first radio frequency (RF) signal applied to a lower electrode within a substrate holder for supporting the substrate; and setting a second power level for a second RF signal applied to an upper electrode opposing the lower electrode above the substrate. The flow rate of one or more constituents of the process gas may be set to a value ranging from about 100 sccm (standard cubic centimeters per minute) to about 500 sccm. The pressure may be set to about 100 mtorr (millitorr) or less. Alternatively, the pressure may be set to about 50 mtorr or less. Alternatively yet, the pressure may be set to about 30 mtorr or less The first power level may be set to about 300 W (watts) or less. Alternatively, the first power level may be set to about 200 W or less. The second power level may be set to a value ranging from about 100 W to about 1000 W. Alternatively, the second power level may be set to a value ranging from about 300 W to about 600 W. Additional details for a plasma processing system are provided below.
As shown in
Once the feature pattern 130 extends through the thickness of the second mask layer 124, the etch time may be extended in order to increase or decrease the difference between the first CD 132 and the second CD 142. By extending the etch time, the inventors have observed that the plasma chemistry and ion bombardment can enlarge the second CD 142 relative to first CD 132.
As shown in
As shown in
Thereafter, substrate 100 may be subjected to one or more ashing processes, one or more stripping processes, one or more dry cleaning processes, or one or more wet cleaning processes, or any combination thereof, in order to remove any remaining portions of the lithographic layer 126, the second mask layer 124, or the optional third mask layer 122.
According to one embodiment, a plasma processing system 1a configured to perform the above identified process conditions is depicted in
Substrate 25 can be affixed to the substrate holder 20 via a clamping system 28, such as a mechanical clamping system or an electrical clamping system (e.g., an electrostatic clamping system). Furthermore, substrate holder 20 can include a heating system (not shown) or a cooling system (not shown) that is configured to adjust and/or control the temperature of substrate holder 20 and substrate 25. The heating system or cooling system may comprise a re-circulating flow of heat transfer fluid that receives heat from substrate holder 20 and transfers heat to a heat exchanger system (not shown) when cooling, or transfers heat from the heat exchanger system to substrate holder 20 when heating. In other embodiments, heating/cooling elements, such as resistive heating elements, or thermo-electric heaters/coolers can be included in the substrate holder 20, as well as the chamber wall of the plasma processing chamber 10 and any other component within the plasma processing system 1a.
Additionally, a heat transfer gas can be delivered to the backside of substrate 25 via a backside gas supply system 26 in order to improve the gas-gap thermal conductance between substrate 25 and substrate holder 20. Such a system can be utilized when temperature control of the substrate is required at elevated or reduced temperatures. For example, the backside gas supply system can comprise a two-zone gas distribution system, wherein the helium gas-gap pressure can be independently varied between the center and the edge of substrate 25.
In the embodiment shown in
Alternately, RF power is applied to the substrate holder electrode at multiple frequencies. Furthermore, impedance match network 32 can improve the transfer of RF power to plasma in plasma processing chamber 10 by reducing the reflected power. Match network topologies (e.g. L-type, π-type, T-type, etc.) and automatic control methods are well known to those skilled in the art.
Gas distribution system 40 may comprise a showerhead design for introducing a mixture of process gases. Alternatively, gas distribution system 40 may comprise a multi-zone showerhead design for introducing a mixture of process gases and adjusting the distribution of the mixture of process gases above substrate 25. For example, the multi-zone showerhead design may be configured to adjust the process gas flow or composition to a substantially peripheral region above substrate 25 relative to the amount of process gas flow or composition to a substantially central region above substrate 25.
Vacuum pumping system 50 can include a turbo-molecular vacuum pump (TMP) capable of a pumping speed up to about 5000 liters per second (and greater) and a gate valve for throttling the chamber pressure. In conventional plasma processing devices utilized for dry plasma etch, a 1000 to 3000 liter per second TMP can be employed. TMPs are useful for low pressure processing, typically less than about 50 mtorr. For high pressure processing (i.e., greater than about 100 mtorr), a mechanical booster pump and dry roughing pump can be used. Furthermore, a device for monitoring chamber pressure (not shown) can be coupled to the plasma processing chamber 10. The pressure measuring device can be, for example, a Type 628B Baratron absolute capacitance manometer commercially available from MKS Instruments, Inc. (Andover, Mass.).
Controller 55 comprises a microprocessor, memory, and a digital I/O port capable of generating control voltages sufficient to communicate and activate inputs to plasma processing system 1a as well as monitor outputs from plasma processing system 1a. Moreover, controller 55 can be coupled to and can exchange information with RF generator 30, impedance match network 32, the gas distribution system 40, vacuum pumping system 50, as well as the substrate heating/cooling system (not shown), the backside gas delivery system 26, and/or the electrostatic clamping system 28. For example, a program stored in the memory can be utilized to activate the inputs to the aforementioned components of plasma processing system 1a according to a process recipe in order to perform a plasma assisted process on substrate 25.
Controller 55 can be locally located relative to the plasma processing system 1a, or it can be remotely located relative to the plasma processing system 1a. For example, controller 55 can exchange data with plasma processing system 1a using a direct connection, an intranet, and/or the internet. Controller 55 can be coupled to an intranet at, for example, a customer site (i.e., a device maker, etc.), or it can be coupled to an intranet at, for example, a vendor site (i.e., an equipment manufacturer). Alternatively or additionally, controller 55 can be coupled to the internet. Furthermore, another computer (i.e., controller, server, etc.) can access controller 55 to exchange data via a direct connection, an intranet, and/or the internet.
In the embodiment shown in
In the embodiment shown in
In the embodiment shown in
For example, the DC voltage applied to upper electrode 70 by DC power supply 90 may range from approximately −2000 volts (V) to approximately 1000 V. Desirably, the absolute value of the DC voltage has a value equal to or greater than approximately 100 V, and more desirably, the absolute value of the DC voltage has a value equal to or greater than approximately 500 V. Additionally, it is desirable that the DC voltage has a negative polarity. Furthermore, it is desirable that the DC voltage is a negative voltage having an absolute value greater than the self-bias voltage generated on a surface of the upper electrode 70. The surface of the upper electrode 70 facing the substrate holder 20 may be comprised of a silicon-containing material.
In the embodiment shown in
In an alternate embodiment, as shown in
Alternately, the plasma can be formed using electron cyclotron resonance (ECR). In yet another embodiment, the plasma is formed from the launching of a Helicon wave. In yet another embodiment, the plasma is formed from a propagating surface wave. Each plasma source described above is well known to those skilled in the art.
In the embodiment shown in
In the following discussion, a method of etching a feature in a multi-layer mask on a substrate utilizing a dry plasma etching system is presented. For example, the dry plasma etching system can comprise various elements, such as described in
In one embodiment, a method of etching a feature pattern in a second mask layer is described, wherein the method uses a process recipe to reduce a first critical dimension (CD) to a second CD. Additionally, the process recipe may reduce an offset between a first CD bias for nested structures in the feature pattern and a second CD bias for isolated structures in the feature pattern. The second mask layer may include a silicon-containing ARC layer.
The process recipe comprises: a process chemistry having a nitrogen-containing gas such as N2, a hydrogen-containing gas such as H2, an optional inert gas, and a CxFyHz-containing gas (e.g., CH2F2, CHF3, etc.). For example, a process parameter space can comprise a chamber pressure of about 5 to about 500 mtorr, a N2 process gas flow rate ranging from about 1 to about 1000 sccm, a H2 process gas flow rate ranging from about 1 to about 1000 sccm, an optional inert process gas flow rate ranging from about 1 to about 1000 sccm, a CxFyHz-containing process gas flow rate ranging from about 1 to about 1000 sccm, a first power level to a lower electrode (e.g., element 20 in
Alternatively, the chamber pressure may be about 100 mtorr or less. Alternatively, the chamber pressure may be about 50 mtorr or less. Alternatively yet, the chamber pressure may be about 30 mtorr or less.
Alternatively, the first power level may be about 300 W or less. Alternatively yet, the first power level may be about 200 W or less.
Alternatively, the second power level may range from about 100 W to about 1000 W. Alternatively yet, the second power level may range from about 300 W to about 600 W.
Alternatively, the process gas flow rate of the nitrogen-containing gas may range from about 10 sccm to about 500 sccm. Alternatively, the process gas flow rate of hydrogen-containing gas may range from about 10 sccm to about 500 sccm. Alternatively, the process gas flow rate of the CxFyHz-containing gas may range from about 1 sccm to about 100 sccm.
In another embodiment, a method of etching a feature pattern in a second mask layer and a third mask layer is described, wherein the method uses a first process recipe for transferring the feature pattern to the second mask layer and a second process recipe for transferring the feature pattern to the third mask layer. The second mask layer may include a silicon-containing ARC layer, and the third mask layer may include an ODL. The first and second process recipes are selected to reduce a CD and an offset between a first critical dimension (CD) bias for nested structures in the feature pattern and a second CD bias for isolated structures in the feature pattern.
The first process recipe comprises: a process chemistry having a nitrogen-containing gas such as N2, a hydrogen-containing gas such as H2, an optional inert gas, and a CxFyHz-containing gas (e.g., CH2F2, CHF3, etc.). For example, a process parameter space can comprise a chamber pressure of about 5 to about 500 mTorr, a N2 process gas flow rate ranging from about 1 to about 1000 sccm, a H2 process gas flow rate ranging from about 1 to about 1000 sccm, an optional inert process gas flow rate ranging from about 1 to about 1000 sccm, a CxFyHz-containing process gas flow rate ranging from about 1 to about 1000 sccm, a first power level to a lower electrode (e.g., element 20 in
Alternatively, the chamber pressure may be about 100 mtorr or less. Alternatively, the chamber pressure may be about 50 mtorr or less. Alternatively yet, the chamber pressure may be about 30 mtorr or less.
Alternatively, the first power level may be about 300 W or less. Alternatively yet, the first power level may be about 200 W or less.
Alternatively, the second power level may range from about 100 W to about 1000 W. Alternatively yet, the second power level may range from about 300 W to about 600 W.
Alternatively, the process gas flow rate of the nitrogen-containing gas may range from about 10 sccm to about 500 sccm. Alternatively, the process gas flow rate of hydrogen-containing gas may range from about 10 sccm to about 500 sccm. Alternatively, the process gas flow rate of the CxFyHz-containing gas may range from about 1 sccm to about 100 sccm.
The second process recipe comprises: a process chemistry having N2, H2, an optional inert gas (e.g., Ar), an optional halogen-containing gas (e.g., HBr), and an optional oxygen-containing gas (e.g., O2). For example, a process parameter space can comprise a chamber pressure of about 5 to about 1000 mtorr, a N2 process gas flow rate ranging from about 1 to about 1000 sccm, a H2 process gas flow rate ranging from about 1 to about 1000 sccm, an optional inert process gas flow rate ranging from about 1 to about 1000 sccm, an optional oxygen-containing process gas flow rate ranging from about 1 to about 1000 sccm, an optional halogen-containing process gas flow rate ranging from about 1 to about 1000 sccm, a first power level to a lower electrode (e.g., element 20 in
Alternatively, for the second process recipe, the chamber pressure may be about 100 mtorr or less. Alternatively, the chamber pressure may be about 50 mtorr or less. Alternatively yet, the chamber pressure may be about 30 mtorr or less.
Alternatively, for the second process recipe, the first power level may be about 200 W or less. Alternatively yet, the first power level may be about 150 W or less.
Alternatively, for the second process recipe, the second power level may range from about 100 W to about 1000 W. Alternatively yet, the second power level may range from about 300 W to about 600 W.
Alternatively, for the second process recipe, the process gas flow rate of N2 may range from about 50 sccm to about 1000 sccm. Alternatively, for the second process recipe, the process gas flow rate of H2 may range from about 10 sccm to about 500 sccm.
In one example, a method is provided for transferring a feature pattern to a silicon-containing ARC layer while reducing the CD, reducing roughness and other defects, and improving selectivity. A photo-resist layer overlies the silicon-containing ARC layer and serves as a lithographic layer, wherein a feature pattern is formed in the photo-resist layer using a lithographic process. An organic dielectric layer (ODL) underlies the silicon-containing ARC layer. The silicon-containing ARC has a silicon content of about 17% by weight. Table 1 provides three process recipes for performing the feature pattern transfer process.
Recipe 1 comprises a conventional silicon-containing ARC layer etch process, wherein the SiARC process step utilizes a process gas having CF4 and CHF3. Recipe 2 comprises another conventional silicon-containing ARC layer etch process, wherein the SiARC process step utilizes a process gas having CF4, CHF3, and Ar. Recipe 3 comprises a new silicon-containing ARC layer etch process, wherein the SiARC process step utilizes a process gas having N2, H2, and CH2F2.
For each process recipe, the etch process is performed in a plasma processing system such as the one shown in
Additionally, Table 1 provides the process condition for each process recipe, including: pressure (mtorr), RF power to the upper electrode (UEL) (W), RF power to the lower electrode (LEL) (W), DC voltage to the upper electrode (V), process gas flow rates (sccm, standard cubic centimeters per minute), center/edge (C/E) (helium) pressure delivered to the backside of the substrate, temperature settings (degrees centigrade, C) for the upper electrode (UEL) (e.g., element 70 in
As shown in Table 2, the CD and the variance in CD (DtD σ) for 130 nm pitch vias and 210 nm pitch vias, respectively, and the corresponding CD shrink Δ and the CD bias offset for dense (i.e., nested) structures and isolated (iso) structures is provided as a result of using each process recipe. Each CD bias presented in Table 2 is a measure of the difference between the initial CD in the lithographic layer and the final CD in the ODL. As observed by the inventors, the CD, the CD variance, the CD shrink Δ, and the CD bias offset are substantially the same for each process recipe. However, the inventors have observed that process recipe 3 provides reduced edge roughness and reduced pattern defects.
Additionally, as shown in Table 2, pattern defects, including the number of open features (i.e., no resulting via) and the relative number of open features, are reduced when using process recipe 3. For each process recipe, the open count, the number of observations, and the ratio of open count to number of observations are provided.
As shown in Table 3, the SiARC etch rate (E/R) (nm/min, nanometers per minute), the photo-resist (PR) etch rate (nm/min), the etch selectivity of the silicon-containing ARC to photo-resist (SiARC/PR), and the percentage (%) of over-etch (O/E) is provided as a result of using each process recipe. The inventors have observed that the etch selectivity between the silicon-containing ARC layer and the photo-resist layer is increased when using process recipe 3. An increase in this etch selectivity (SiARC/PR) reduces the consumption of the photo-resist layer. Further, the inventors have observed that the etch selectivity between the silicon-containing ARC layer and the underlying ODL (SiARC/ODL) is increased when using process recipe 3. An increase in this etch selectivity (SiARC/ODL) allows the pattern transfer to the silicon-containing ARC layer to uniformly land on the silicon-containing ARC layer/ODL interface.
Although only certain embodiments of this invention have been described in detail above, those skilled in the art will readily appreciate that many modifications are possible in the embodiments without materially departing from the novel teachings and advantages of this invention. Accordingly, all such modifications are intended to be included within the scope of this invention.