Classifications

• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
  • H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
  • H01J37/32—Gas-filled discharge tubes
  • H01J37/32431—Constructional details of the reactor
  • H01J37/3244—Gas supply means
  • H01J37/32449—Gas control, e.g. control of the gas flow
• • 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
  • H10P76/00—Manufacture or treatment of masks on semiconductor bodies, e.g. by lithography or photolithography
  • H10P76/40—Manufacture or treatment of masks on semiconductor bodies, e.g. by lithography or photolithography of masks comprising inorganic materials
  • H10P76/408—Manufacture or treatment of masks on semiconductor bodies, e.g. by lithography or photolithography of masks comprising inorganic materials characterised by their sizes, orientations, dispositions, behaviours or shapes
  • H10P76/4085—Manufacture or treatment of masks on semiconductor bodies, e.g. by lithography or photolithography of masks comprising inorganic materials characterised by their sizes, orientations, dispositions, behaviours or shapes characterised by the processes involved to create the masks
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
  • H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
  • H01J37/32—Gas-filled discharge tubes
  • H01J37/32431—Constructional details of the reactor
  • H01J37/32715—Workpiece holder
  • H01J37/32724—Temperature
• • 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
  • C23C16/26—Deposition of carbon only
• • 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
  • C23C16/26—Deposition of carbon only
  • C23C16/27—Diamond only
  • C23C16/272—Diamond only using DC, AC or RF discharges
• • C—CHEMISTRY; METALLURGY
  • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
  • C23C16/44—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
  • C23C16/458—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for supporting substrates in the reaction chamber
  • C23C16/4582—Rigid and flat substrates, e.g. plates or discs
  • C23C16/4583—Rigid and flat substrates, e.g. plates or discs the substrate being supported substantially horizontally
  • C23C16/4586—Elements in the interior of the support, e.g. electrodes, heating or cooling devices
• • 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
  • C23C16/46—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for heating the substrate
  • C23C16/463—Cooling of the substrate
• • 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
  • C23C16/509—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 using internal electrodes
• • C—CHEMISTRY; METALLURGY
  • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
  • C23C16/56—After-treatment
• • G—PHYSICS
  • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
  • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
  • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
  • G03F7/20—Exposure; Apparatus therefor
• • G—PHYSICS
  • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
  • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
  • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
  • G03F7/70—Microphotolithographic exposure; Apparatus therefor
  • G03F7/70691—Handling of masks or workpieces
• • H—ELECTRICITY
  • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
  • H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
  • H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
  • H10P14/60—Formation of materials, e.g. in the shape of layers or pillars of insulating materials
  • H10P14/63—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the formation processes
  • H10P14/6326—Deposition processes
  • H10P14/6328—Deposition from the gas or vapour phase
  • H10P14/6334—Deposition from the gas or vapour phase using decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition
  • H10P14/6336—Deposition from the gas or vapour phase using decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition in the presence of a plasma [PECVD]
• • H—ELECTRICITY
  • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
  • H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
  • H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
  • H10P14/60—Formation of materials, e.g. in the shape of layers or pillars of insulating materials
  • H10P14/69—Inorganic materials
  • H10P14/6902—Inorganic materials composed of carbon, e.g. alpha-C, diamond or hydrogen doped carbon
• • 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
  • H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
  • H10P72/00—Handling or holding of wafers, substrates or devices during manufacture or treatment thereof
  • H10P72/04—Apparatus for manufacture or treatment
  • H10P72/0431—Apparatus for thermal treatment
  • H10P72/0432—Apparatus for thermal treatment mainly by conduction
• • 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
  • H10P72/00—Handling or holding of wafers, substrates or devices during manufacture or treatment thereof
  • H10P72/70—Handling or holding of wafers, substrates or devices during manufacture or treatment thereof for supporting or gripping
  • H10P72/72—Handling or holding of wafers, substrates or devices during manufacture or treatment thereof for supporting or gripping using electrostatic chucks
• • 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
  • H10P72/00—Handling or holding of wafers, substrates or devices during manufacture or treatment thereof
  • H10P72/70—Handling or holding of wafers, substrates or devices during manufacture or treatment thereof for supporting or gripping
  • H10P72/72—Handling or holding of wafers, substrates or devices during manufacture or treatment thereof for supporting or gripping using electrostatic chucks
  • H10P72/722—Details of electrostatic chucks
• • 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
  • H10P76/00—Manufacture or treatment of masks on semiconductor bodies, e.g. by lithography or photolithography
  • H10P76/40—Manufacture or treatment of masks on semiconductor bodies, e.g. by lithography or photolithography of masks comprising inorganic materials
  • H10P76/405—Manufacture or treatment of masks on semiconductor bodies, e.g. by lithography or photolithography of masks comprising inorganic materials characterised by their composition, e.g. multilayer masks
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
  • H01J2237/00—Discharge tubes exposing object to beam, e.g. for analysis treatment, etching, imaging
  • H01J2237/18—Vacuum control means
  • H01J2237/182—Obtaining or maintaining desired pressure
  • H01J2237/1825—Evacuating means
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
  • H01J2237/00—Discharge tubes exposing object to beam, e.g. for analysis treatment, etching, imaging
  • H01J2237/245—Detection characterised by the variable being measured
  • H01J2237/24571—Measurements of non-electric or non-magnetic variables
  • H01J2237/24585—Other variables, e.g. energy, mass, velocity, time, temperature
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
  • H01J2237/00—Discharge tubes exposing object to beam, e.g. for analysis treatment, etching, imaging
  • H01J2237/32—Processing objects by plasma generation
  • H01J2237/33—Processing objects by plasma generation characterised by the type of processing
  • H01J2237/332—Coating
  • H01J2237/3321—CVD [Chemical Vapor Deposition]
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
  • H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
  • H01J37/32—Gas-filled discharge tubes
  • H01J37/32009—Arrangements for generation of plasma specially adapted for examination or treatment of objects, e.g. plasma sources
  • H01J37/32082—Radio frequency generated discharge
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
  • H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
  • H01J37/32—Gas-filled discharge tubes
  • H01J37/32431—Constructional details of the reactor
  • H01J37/3244—Gas supply means
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
  • H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
  • H01J37/32—Gas-filled discharge tubes
  • H01J37/32431—Constructional details of the reactor
  • H01J37/32798—Further details of plasma apparatus not provided for in groups H01J37/3244 - H01J37/32788; special provisions for cleaning or maintenance of the apparatus
  • H01J37/32816—Pressure
  • H01J37/32834—Exhausting
• • 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
• • 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
  • H10P72/00—Handling or holding of wafers, substrates or devices during manufacture or treatment thereof
  • H10P72/06—Apparatus for monitoring, sorting, marking, testing or measuring
  • H10P72/0602—Temperature monitoring
• • 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
  • H10P76/00—Manufacture or treatment of masks on semiconductor bodies, e.g. by lithography or photolithography
  • H10P76/20—Manufacture or treatment of masks on semiconductor bodies, e.g. by lithography or photolithography of masks comprising organic materials
  • H10P76/204—Manufacture or treatment of masks on semiconductor bodies, e.g. by lithography or photolithography of masks comprising organic materials of organic photoresist masks

Definitions

• Embodiments of the present disclosure generally relate to the fabrication of integrated circuits. More particularly, the embodiments described herein provide techniques for deposition of high-density carbon films for patterning applications.
• Integrated circuits have evolved into complex devices that can include millions of transistors, capacitors and resistors on a single chip.
• the evolution of chip designs continually requires faster circuitry and greater circuit density.
• the demands for faster circuits with greater circuit densities impose corresponding demands on the process sequences used in the manufacture of integrated circuit components.
• a layer of energy sensitive resist is formed over a stack of material layers disposed on a substrate.
• the energy sensitive resist layer is exposed to an image of a pattern to form a photoresist mask. Thereafter, the mask pattern is transferred to one or more of the material layers of the stack using an etch process.
• the thickness of the energy sensitive resist is correspondingly reduced in order to control pattern resolution.
• Such thin resist layers can be insufficient to mask underlying material layers during the pattern transfer operation due to attack by the chemical etchant.
• a hardmask is often used between the energy sensitive resist layer and the underlying material layers to facilitate pattern transfer because of greater resistance to the chemical etchant.
• critical dimensions (CD) decrease, current hardmask materials lack the desired etch selectivity relative to underlying materials (e.g., oxides and nitrides) and are often difficult to deposit.
• Embodiments of the present disclosure generally relate to the fabrication of integrated circuits. More particularly, the embodiments described herein provide techniques for deposition of high-density films for patterning applications. In one embodiment, a method of forming a carbon film on a substrate is provided.
• the method includes flowing a hydrocarbon-containing gas mixture into a process chamber having a substrate positioned on an electrostatic chuck, wherein the substrate is maintained at a temperature of about -10 °C to about 20 °C and a chamber pressure of about 0.5 mTorr to about 10 Torr, and generating a plasma by applying a first RF bias to the electrostatic chuck to deposit a diamond-like carbon film containing about 60% or greater hybridized sp 3 atoms on the substrate, wherein the first RF bias is provided at a power of about 1800 Watts to about 2200 Watts for a 300 mm substrate and at a frequency of about 40 MFIz to about 162 MFIz.
• the method includes flowing a hydrocarbon- containing gas mixture into a processing volume of a process chamber having a substrate positioned on an electrostatic chuck, and generating a plasma by applying a first RF bias to the electrostatic chuck and a second RF bias to an electrode disposed above and opposing the electrostatic chuck to deposit a diamond-like carbon film on the substrate, wherein first RF bias is provided at a frequency of about 13.56 MFIz or below and the second RF bias is provided at a frequency of about 40 MFIz or above, and the substrate is maintained at a temperature of about -10 °C to about 20 °C and a chamber pressure of about 0.5 mTorr to about 10 Torr.
• the method includes flowing a hydrocarbon- containing gas mixture into a processing volume of a process chamber having a substrate positioned on an electrostatic chuck, wherein the substrate is maintained at a pressure between about 5 mTorr, and wherein the hydrocarbon-containing gas mixture comprises acetylene (C2FI2), generating a plasma at the substrate level by applying a first RF bias to the electrostatic chuck to deposit a diamond-like carbon film on the substrate, wherein the first RF bias is provided at a power between about 2000 Watts and a frequency of about 60 MFIz, forming a patterned photoresist layer over the diamond-like carbon film, etching the diamond-like carbon in a pattern corresponding with the patterned photoresist layer, etching the pattern into the substrate, and depositing a material into the etched portions of the diamond-like carbon film.
• C2FI2 acetylene
• Figure 1 A depicts a schematic cross-sectional view of a deposition system that can be used for the practice of embodiments described herein;
• Figure 1 B depicts a schematic cross-sectional view of another deposition system that can be used for the practice of embodiments described herein;
• Figure 2 depicts a schematic cross-sectional view of an electrostatic chuck that may be used in the apparatus of Figure 1A and Figure 1 B for the practice of embodiments described herein;
• Figure 3 depicts a flow diagram of a method for forming a diamond-like carbon layer on a film stack disposed on a substrate in accordance with one or more embodiments of the present disclosure
• Figures 4A-4B depict one embodiment of a sequence for forming a diamond-like carbon layer on a film stack formed on a substrate in accordance with one or more embodiments of the present disclosure
• the following disclosure describes techniques for deposition of diamond- like carbon films on a substrate. Embodiments described herein will be described below in reference to a PECVD process that can be carried out using any suitable thin film deposition system.
• suitable systems include the CENTURA ® systems which may use a DXZ ® processing chamber, PRECISION 5000 ® systems, PRODUCER ® systems, PRODUCER ® GTTM systems, PRODUCER ® XP PrecisionTM systems, PRODUCER ® SETM systems, Sym3 ® processing chamber, and MesaTM processing chamber, all of which are commercially available from Applied Materials, Inc., of Santa Clara, Calif.
• FIG. 1 A depicts a schematic illustration of a substrate processing system 132 that can be used to perform diamond-like carbon layer deposition in accordance with embodiments described herein.
• the substrate processing system 132 includes a process chamber 100 coupled to a gas panel 130 and a controller 1 10.
• the process chamber 100 generally includes a top wall 124, a sidewall 101 and a bottom wall 122 that define a processing volume 126.
• a substrate support assembly 146 is provided in the processing volume 126 of the process chamber 100.
• the substrate support assembly 146 generally includes an electrostatic chuck 150 supported by a stem 160.
• the electrostatic chuck 150 may be typically fabricated from aluminum, ceramic, and other suitable materials such as stainless steel.
• the electrostatic chuck 150 may be moved in a vertical direction inside the process chamber 100 using a displacement mechanism (not shown).
• a vacuum pump 102 is coupled to a port formed in the bottom of the process chamber 100.
• the vacuum pump 102 is used to maintain a desired gas pressure in the process chamber 100.
• the vacuum pump 102 also evacuates post-processing gases and by-products of the process from the process chamber 100.
• a gas distribution assembly 120 having a plurality of apertures 128 is disposed on the top of the process chamber 100 above the electrostatic chuck 150.
• the apertures 128 of the gas distribution assembly 120 are utilized to introduce process gases into the process chamber 100.
• the apertures 128 may have different sizes, number, distributions, shape, design, and diameters to facilitate the flow of the various process gases for different process requirements.
• the gas distribution assembly 120 is connected to the gas panel 130 that allows various gases to flow to the processing volume 126 during processing.
• a plasma is formed from the process gas mixture exiting the gas distribution assembly 120 to enhance thermal decomposition of the process gases resulting in the deposition of material on a top surface 191 of a substrate 190 positioned on the electrostatic chuck 150.
• the gas distribution assembly 120 and the electrostatic chuck 150 may form a pair of spaced apart electrodes in the processing volume 126.
• One or more RF power source 140 provides a bias potential through a matching network 138, which is optional, to the gas distribution assembly 120 to facilitate generation of plasma between the gas distribution assembly 120 and the electrostatic chuck 150.
• the RF power source 140 and the matching network 138 may be coupled to the gas distribution assembly 120, the electrostatic chuck 150, or coupled to both the gas distribution assembly 120 and the electrostatic chuck 150, or coupled to an antenna (not shown) disposed exterior to the process chamber 100.
• the RF power source 140 may produce power at a frequency of 350 KHz, 2 MHz, 13.56 MHz, 27 MHz, 40 MHz, 60 MHz, 100 MHz, or 162 MHz.
• the controller 1 10 includes a central processing unit (CPU) 1 12, a memory 1 16, and a support circuit 1 14 utilized to control the process sequence and regulate the gas flows from the gas panel 130.
• the CPU 1 12 may be of any form of a general- purpose computer processor that may be used in an industrial setting.
• the software routines can be stored in the memory 1 16, such as random access memory, read only memory, floppy, or hard disk drive, or other form of digital storage.
• the support circuit 1 14 is coupled to the CPU 1 12 and may include cache, clock circuits, input/output systems, power supplies, and the like. Bi-directional communications between the controller 1 10 and the various components of the substrate processing system 132 are handled through numerous signal cables collectively referred to as signal buses 1 18, some of which are illustrated in Figure 1A.
• Figure 1 B depicts a schematic cross-sectional view of another substrate processing system 180 that can be used for the practice of embodiments described herein.
• the substrate processing system 180 is similar to the substrate processing system 132 of Figure 1A, except that the substrate processing system 180 is configured to radially flow processing gases from gas panel 130 across the top surface 191 of the substrate 190 via the sidewall 101.
• the gas distribution assembly 120 depicted in Figure 1A is replaced with an electrode 182.
• the electrode 182 may be configured for secondary electron generation.
• the electrode 182 is a silicon-containing electrode.
• FIG. 2 depicts a schematic cross-sectional view of the substrate support assembly 146 used in the processing systems of Figure 1 A and Figure 1 B that can be used for the practice of embodiments described herein.
• the electrostatic chuck 150 may include a heater element 170 suitable for controlling the temperature of the substrate 190 supported on an upper surface 192 of the electrostatic chuck 150.
• the heater element 170 may be embedded in the electrostatic chuck 150.
• the electrostatic chuck 150 may be resistively heated by applying an electric current from a heater power source 106 to the heater element 170.
• the heater power source 106 may be coupled through an RF filter 216 to protect the heater power source 106 from RF energy.
• the electric current supplied from the heater power source 106 is regulated by the controller 1 10 to control the heat generated by the heater element 170, thus maintaining the substrate 190 and the electrostatic chuck 150 at a substantially constant temperature during film deposition.
• the supplied electric current may be adjusted to selectively control the temperature of the electrostatic chuck 150 between about -50 °C to about 350 °C during deposition of diamond-like carbon films on the substrate.
• a temperature sensor 172 such as a thermocouple, may be embedded in the electrostatic chuck 150 to monitor the temperature of the electrostatic chuck 150. The measured temperature is used by the controller 1 10 to control the power supplied to the heater element 170 to maintain the substrate at a desired temperature.
• the electrostatic chuck 150 includes a chucking electrode 210, which may be a mesh of a conductive material.
• the chucking electrode 210 may be embedded in the electrostatic chuck 150.
• the chucking electrode 210 is coupled to a chucking power source 212 that, when energized, electrostatically clamps the substrate 190 to the upper surface 192 of the electrostatic chuck 150.
• the chucking electrode 210 may be configured as a monopolar or bipolar electrode, or have another suitable arrangement.
• the chucking electrode 210 may be coupled through an RF filter 214 to the chucking power source 212, which provides direct current (DC) power to electrostatically secure the substrate 190 to the upper surface 192 of the electrostatic chuck 150.
• the RF filter 214 prevents RF power utilized to form plasma within the process chamber 100 from damaging electrical equipment.
• the electrostatic chuck 150 may be fabricated from a ceramic material, such as AIN or AI2O3.
• a power application system 220 is coupled to the substrate support assembly 146.
• the power application system 220 may include the heater power source 106, the chucking power source 212, a first radio frequency (RF) power source 230, and a second RF power source 240.
• Embodiments of the power application system 220 may additionally include the controller 1 10, and a sensor device 250 that is in communication with the controller 1 10 and both of the first RF power source 230 and the second RF power source 240.
• the controller 1 10 may also be utilized to control the plasma from the processing gas by application of RF power from the first RF power source 230 and the second RF power source 240 in order to deposit a layer of material on the substrate 190.
• the electrostatic chuck 150 includes the chucking electrode 210 that may function in one aspect to chuck the substrate 190 while also functioning as a first RF electrode.
• the electrostatic chuck 150 may also include a second RF electrode 260, and together with the chucking electrode 210, may apply RF power to tune the plasma.
• the first RF power source 230 may be coupled to the second RF electrode 260 while the second RF power source 240 may be coupled to the chucking electrode 210.
• a first matching network and a second matching network may be provided for the first RF power source 230 and the second RF power source 240, respectively.
• the second RF electrode 260 may be a solid metal plate of a conductive material or a mesh of conductive material.
• the first RF power source 230 and the second RF power source 240 may produce power at the same frequency or a different frequency.
• one or both of the first RF power source 230 and the second RF power source 240 may independently produce power at a frequency from about 350 KFIz to about 162 MHz (e.g., 350 KHz, 2 MHz, 13.56 MHz, 27 MHz, 40 MHz, 60 MHz, 100 MHz, or 162 MHz).
• RF power from one or both of the first RF power source 230 and second RF power source 240 may be varied in order to tune the plasma.
• the systems described with respect to Figures 1A, 1 B, and 2 may be used to deposit carbon films according to embodiments described herein.
• the carbon films e.g., one or more carbon layers
• fabricated according to the embodiments described herein are amorphous in nature and have a high sp 3 carbon conten (e.g., diamond-like).
• the as-deposited diamond-like carbon layer has an extinction coefficient or k-value (K (at 633 nm)) less than 0.1 , for example 0.09, a density (g/cc) of greater than 1 .8 g/cc, for example approximately 2.0 g/cc or higher, approximately 2.5 g/cc or higher, such as from about 1 .8 g/cc to about 2.5 g/cc, a refractive index or n-value (n (at 633 nm)) greater than 2.0, for example, approximately 2.0 to approximately 3.0, such as 2.3, a stress (MPa) less than about -100 MPa, for example from about -1000 MPa to about -100 MPa, such as about -550 MPa, and an elastic modulus (GPa) of about 150 GPa or greater, for example, from about 200 to about 400 GPa.
• K extinction coefficient or k-value
• the as-deposited diamond-like carbon layer may contain at least 40 percent of sp 3 hybridized carbon atoms or more, such as about 60 percent or more, for example about 90 percent of sp 3 hybridized carbon atoms.
• the as deposited diamond-like carbon layer may have a thickness between about 5 A and about 20,000 A.
• the diamond-like carbon layer with characteristics above can be formed using the following exemplary deposition process parameters.
• the substrate temperature may range from about -50 °C to about 350 °C (e.g., from about -10 °C to about 20 °C).
• the chamber pressure may range from a chamber pressure of about 0.5 mTorr to about 10 Torr (e.g., about 5 mTorr to about 10 mTorr).
• the flow rate of the hydrocarbon-containing gas mixture may be from about 10 seem to about 1 ,000 seem (e.g., about 100 seem to about 200 seem).
• the flow rate of a dilution gas may individually range from about 50 seem to about 5000 seem (e.g., from about 50 seem to about 200 seem).
• Table I illustrates exemplary deposition process parameters, which are performed on a 300 mm substrate in a deposition chamber available from Applied Materials, Inc. of Santa Clara, CA.
• Figure 3 depicts a flow diagram of a method 300 for forming a diamond-like carbon layer on a film stack disposed on a substrate in accordance with one embodiment of the present disclosure.
• the diamond-like carbon layer formed on a film stack may be utilized, for example, as a hardmask to form stair-like structures in the film stack.
• Figures 4A-4B are schematic cross-sectional views illustrating a sequence for forming a diamond-like carbon layer on a film stack disposed on a substrate according to the method 300. It should also be understood that the operations depicted in Figure 3 may be performed simultaneously and/or in a different order than the order as depicted.
• the method 300 begins at operation 310 by positioning a substrate, such as a substrate 400 depicted in Figure 4A, into a process chamber, such as the process chamber 100 depicted in Figure 1A or Figure 1 B.
• the substrate 400 may be substrate 190 depicted in Figure 1A, Figure 1 B and Figure 2.
• the substrate 400 may be positioned on an electrostatic chuck, for example, the upper surface 192 of the electrostatic chuck 150.
• the substrate 400 may be a silicon-based material or any suitable insulating material, conductive material, or semiconductor material as needed, having a film stack 404 disposed on the substrate 400 that may be utilized to form a structure 402, such as stair-like structures, in the film stack 404.
• the substrate 400 may have a substantially planar surface, an uneven surface, or a substantially planar surface having a structure formed thereon.
• the film stack 404 is formed on the substrate 400.
• the film stack 404 may be utilized to form a gate structure, a contact structure or an interconnection structure in a front end or back end process.
• the method 300 may be performed on the film stack 404 to form the stair-like structures therein used in a memory structure, such as NAND structure.
• the substrate 400 may be a material such as crystalline silicon (e.g., Si ⁇ 100> or Si ⁇ 1 1 1 >), silicon oxide, strained silicon, silicon germanium, doped or undoped polysilicon, doped or undoped silicon substrates and patterned or non-patterned substrates silicon on insulator (SOI), carbon doped silicon oxides, silicon nitride, doped silicon, germanium, gallium arsenide, glass, sapphire.
• SOI silicon on insulator
• the substrate 400 may have various dimensions, such as 200 mm, 300 mm, and 450 mm or other diameter substrates, as well as, rectangular or square panels.
• the substrate 400 may include a buried dielectric layer disposed on a silicon crystalline substrate.
• the substrate 400 may be a crystalline silicon substrate.
• the film stack 404 disposed on the substrate 400 may have a number of vertically stacked layers.
• the film stack 404 may comprise pairs including a first layer (shown as 408ai , 408a2, 408a3, . , 408a n ) and a second layer
• the pairs includes alternating first layer (shown as 408ai, 408a2, 408a3, . , 408a n ) and second layer (shown as 408bi, 408b2, 408b3, . , 408b n ) repeatedly formed until desired numbers of pairs of the first layers and the second layers are reached.
• the film stack 404 may be a part of a semiconductor chip, such as a three- dimensional memory chip. Although three repeating layers of first layers (shown as
• the film stack 404 may be utilized to form multiple gate structures for a three-dimensional memory chip.
• . , 408a n , formed in the film stack 404 may be a first dielectric layer and the second layers 408bi , 408b2, 408b3, . , 408b n may be a second dielectric layer. Suitable dielectric layers may be utilized to form the first layers 408ai , 408a2, 408a3, . , 408a n and the second layer 408bi , 408b2, 408b3, .
• the dielectric layers may be a high-k material having a dielectric constant greater than 4.
• the high-k materials include hafnium dioxide (Hf02), zirconium dioxide (Zr02), hafnium silicon oxide (HfSi02), hafnium aluminum oxide (HfAIO), zirconium silicon oxide (ZrSi02), tantalum dioxide (Ta02), aluminum oxide, aluminum doped hafnium dioxide, bismuth strontium titanium (BST), and platinum zirconium titanium (PZT), among others.
• the first layers 408a-i , 408a2, 408a3, . , 408a n are silicon oxide layers and the second layers 408bi , 408b2, 408b3, . , 408b n are silicon nitride layers or polysilicon layers disposed on the first layers 408a-i , 408a2,
• 408a3, . , 408a n may be controlled at between about 50 A and about 1000 A, such as about 500 A, and the thickness of the each second layers 408bi , 408b2,
• the film stack 404 may have a total thickness between about 100 A and about 2000 A and may vary as technology advances.
• the diamond-like carbon layer may be formed on any surfaces or any portion of the substrate 400 with or without the film stack 404 present on the substrate 400.
• a chucking voltage is applied to the electrostatic chuck to clamp the substrate 400 to the electrostatic chuck.
• An electrical bias is provided to the substrate 400 via chucking electrode 210.
• the chucking electrode 210 may be in electronic communication with the chucking power source 212 that supplies a biasing voltage to the chucking electrode 210.
• the chucking voltage is between about 10 volts and about 3000 volts.
• the process pressure in the processing volume may be maintained at about 0.1 mTorr to about 10 Torr (e.g about 0.5 mTorr to about 15 mTorr), and the processing temperature and/or substrate temperature may be maintained at about -50 °C to about 350 °C (e.g., about -10 °C to about 20 °C).
• a hydrocarbon-containing gas mixture is flowed into the processing volume 126.
• the hydrocarbon-containing gas mixture may be flowed from the gas panel 130 into the processing volume 126 either through the gas distribution assembly 120 or via the sidewall 101 .
• the hydrocarbon-containing gas mixture may include at least one hydrocarbon compound.
• the hydrocarbon-containing gas mixture may further include an inert gas, a dilution gas, or any combinations thereof.
• the chucking voltage supplied during operation 320 is maintained during operation 330.
• the hydrocarbon compound is a gaseous hydrocarbon.
• the hydrocarbon compound has a general formula CxH y , where x has a range of between 1 and 20 and y has a range of between 1 and 20.
• Suitable hydrocarbon compounds include, for example, C2H2, C3H6, CH 4 , C4H8, 1 ,3- dimethyladamantane, bicyclo[2.2.1 ]hepta-2, 5-diene (2,5-Norbornadiene), adamantine (C10H16), norbornene (C7H10), or combinations thereof.
• the hydrocarbon-containing gas mixture further comprises one or more dilution gases.
• Suitable dilution gases may include, but are not limited to, helium (He), argon (Ar), xenon (Xe), hydrogen (H2), nitrogen (N2), ammonia (NH3), or any combinations thereof.
• the dilution gas includes a combination of Ar, He, and N2.
• the dilution gas includes a combination of Ar, He, and H2.
• the hydrocarbon-containing gas mixture further comprises an inert gas.
• an inert gas such as argon (Ar) and/or helium (He) may be supplied with the hydrocarbon-containing gas mixture into the processing volume 126.
• Other inert gases such as nitrogen (N2) and nitric oxide (NO), may also be used to control the density and deposition rate of the diamond-like carbon layer.
• a plasma is generated at the substrate level to form the diamond-like carbon film on the film stack as shown in Figure 4B.
• Plasma may be generated by applying a first RF bias to the electrostatic chuck.
• the first RF bias may be from about 10 Watts and about 3000 Watts at a frequency of from about 350 KHz to about 162 MHz (e.g., 350 KHz, 2 MHz, 13.56 MHz, 27 MHz, 40 MHz, 60 MHz, 100 MHz, or 162 MHz).
• the first RF bias is provided at a power between about 1500 Watts and about 2500 Watts (e.g., 1800-2200 Watts) and at a frequency of about 40 MHz or above.
• the first RF bias is provided to the electrostatic chuck 150 via the second RF electrode 260.
• the second RF electrode 260 may be in electronic communication with the first RF power source 230 that supplies a biasing voltage to the second RF electrode 260.
• the first RF power source 230 may produce power at a frequency of from about 350 KFIz to about 100 MHz (e.g., 350 KHz, 2 MHz, 13.56 MHz, 27 MHz, 40 MHz, 60 MHz, or 100 MHz).
• operation 340 further comprises applying a second RF bias to the electrostatic chuck to independently control ion density and ion energy to modulate film stress.
• the second RF bias may be from about 10 Watts and about 3000 Watts and at a frequency of from about 350 KHz to about 100 MHz (e.g., 350 KHz, 2 MHz, 13.56 MHz, 27 MHz, 40 MHz, 60 MHz, or 100 MHz).
• the second RF bias is provided at a power between about 800 Watts and about 1200 Watts and at a frequency of about 13.56 MHz or below, for example about 2 MHz.
• the second RF bias is provided to the substrate 400 via the chucking electrode 210.
• the chucking electrode 210 may be in electronic communication with second RF power source 240 that supplies a biasing voltage to the chucking electrode 210.
• the second RF bias is provided at a power between about 10 Watts and about 3000 Watts. In one embodiment, the second RF bias is provided at a power between about 800 Watts and about 1200 Watts. In one embodiment, the chucking voltage supplied in operation 320 is maintained during operation 340.
• the first RF bias is provided to the substrate 400 via the chucking electrode 210 and the second RF bias may be provided to the substrate 400 via the second RF electrode 260.
• the first RF bias is provided to the gas distribution assembly 120 or the electrode 182
• the second RF bias may be provided to the substrate 400 via the second RF electrode 260 or the chucking electrode 210.
• the first RF bias applying to the gas distribution assembly 120 or the electrode 182 can have a high frequency
• the second RF bias applying to second RF electrode 260 or the chucking electrode 210 can have a low frequency.
• Various combinations of power level and frequency can be used by the first RF bias and the second RF bias.
• the first RF bias can be about 2000 Watts at about 40 MFIz, 60 MFIz, or 162 MFIz
• the second RF bias can be about 1000 Watts at 350 KFIz.
• the first RF bias can be about 2000 Watts at 40 MFIz, 60 MFIz, or 162 MFIz
• the second RF bias can be about 1000 Watts at 2 MFIz.
• the first RF bias can be about 2000 Watts at about 40 MFIz, 60 MFIz, or 162 MFIz
• the second RF bias can be about 1000 Watts at 13.56 MFIz.
• the first RF bias is provided to the substrate 400 via the chucking electrode 210
• the second RF bias may be provided to the substrate 400 via the second RF electrode 260
• a third RF bias may be provided to the gas distribution assembly 120 or the electrode 182.
• the first RF bias and the second RF bias can be any combinations of frequencies and power discussed in this disclosure
• the third RF bias may be configured to have power and frequency identical to that of the first or second RF bias discussed herein.
• the diamond-like carbon layer 412 is exposed to hydrogen radicals.
• the diamond-like carbon layer is exposed to hydrogen radicals during the deposition process of operation 340.
• the hydrogen radicals are formed in an RPS and delivered to the processing region. Not to be bound by theory, but it is believed that exposing the diamond-like carbon layer to hydrogen radicals leads to selective etching of sp 2 hybridized carbon atoms thus increasing the sp 3 hybridized carbon atom fraction of the film, thus increasing the etch selectivity.
• the substrate is de-chucked.
• the chucking voltage is turned-off.
• the reactive gases are turned-off and optionally purged from the processing chamber.
• RF power is reduced (e.g ⁇ 200 W).
• the remaining gases are purged from the processing chamber.
• the processing chamber is pumped down and the substrate is moved up on the lift pins and transferred out of the process chamber.
• the diamond-like carbon layer 412 may be utilized in an etching process as a patterning mask to form a three-dimensional structure, such as a stair like structure.
• the diamond-like carbon layer 412 may be patterned using a standard photoresist patterning techniques.
• a low stress, high-density diamond-like carbon film of the present disclosure was fabricated by flowing 150 seem C2H2 and 100 seem He as process gases at a temperature of 10 °C, applying 2000 Watts RF (60 MHz) power through the substrate pedestal (electrostatic chuck) in a CVD reactor with Ar and/or He as diluting gas. Comparison between the resultant diamond-like carbon film, amorphous carbon reference films and diamond-like carbon films formed by PVD are illustrated in Table II below.

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