Photoresist development with organic vapors.

Abstract

Resist development is useful, for example, for forming patterning masks in high-resolution patterning applications. Development can be achieved using an organic vapor, such as a carboxylic acid. In some embodiments, the organic vapor is trifluoroacetic acid. In some embodiments, the organic vapor is hexafluoroacetylacetone. Metal-containing resist films, such as EUV-sensitive organometallic oxides, can be deposited on semiconductor substrates using dry or wet deposition techniques. Metal-containing resist films on semiconductor substrates can be developed using organic vapors, or residues of metal-containing resist materials formed on process chamber surfaces can be removed using organic vapors.

Description

[Technical Field]

[0001] Incorporation by Reference A PCT application is being filed concurrently herewith as part of this application, and each application identified in that concurrently filed PCT application to which this application claims benefit or priority is incorporated herein by reference in its entirety for all purposes. [Background technology]

[0002] The fabrication of semiconductor devices, such as integrated circuits, is a multi-step process involving photolithography. Generally, this process involves depositing material onto a wafer and lithographically patterning the material to form structural features (e.g., transistors and circuits) of the semiconductor device. Typical photolithography process steps known in the art include preparing a substrate onto which a photoresist is applied, such as by spin coating; exposing the photoresist to light in a desired pattern to render the exposed areas of the photoresist somewhat soluble in a developer; developing by applying a developer to remove either the exposed or unexposed areas of the photoresist; and subsequent processing, such as by etching or material deposition, to form features on the areas of the substrate from which the photoresist was removed.

[0003] The evolution of semiconductor design is driven by the need for, and ability to, form ever smaller features on semiconductor substrate materials. This technological advance is characterized in "Moore's Law" as the doubling of transistor density in high-density integrated circuits every two years. In fact, chip design and manufacturing have advanced to the point where modern microprocessors can contain billions of transistors and other circuit features on a single chip. Individual features on such chips can be on the order of 22 nanometers (nm) or smaller, and in some cases less than 10 nm.

[0004] One challenge in fabricating devices with such small features is the ability to reliably and reproducibly form photolithography masks with sufficient resolution. Current photolithography processes typically use 193 nm ultraviolet (UV) light to expose photoresist. The fact that the light has a wavelength significantly longer than the desired size of the features to be fabricated on the semiconductor substrate presents inherent problems. Achieving feature sizes smaller than the wavelength of light requires the use of complex resolution enhancement techniques, such as multi-patterning. Therefore, there has been significant interest and research effort in developing photolithography techniques that use short-wavelength light, such as extreme ultraviolet (EUV) light, with wavelengths of 10 nm to 15 nm, e.g., 13.5 nm.

[0005] However, EUV photolithography processes can have challenges, such as reduced power output and light loss during patterning. Conventional organic chemically amplified resists (CARs), similar to those used in 193 nm UV lithography, have potential drawbacks when used with EUV lithography because they have low absorption coefficients, especially in the EUV region, and can result in blurring or line-edge roughness due to diffusion of photoactivated species. Furthermore, to provide the etch resistance necessary to pattern underlying device layers, small features patterned with conventional CAR materials can result in high aspect ratios that risk pattern collapse. Therefore, there remains a need for improved EUV photoresist materials with properties such as reduced thickness, greater absorbance, and greater etch resistance.

[0006] The background description provided herein is intended to provide a general overview of the present technology. Work by the currently named inventors within the scope of what is described in this background section, as well as aspects of the description that may not otherwise be considered prior art at the time of filing, are not admitted, expressly or impliedly, as prior art against the present technology. Summary of the Invention

[0007] Provided herein is a method for developing a photopatterned metal-containing resist, the method including providing a photopatterned metal-containing resist on a surface of a semiconductor substrate in a process chamber, and dry developing the resist by selectively removing portions of the photopatterned metal-containing resist by exposure to a developing chemistry comprising an organic vapor to form a resist mask.

[0008] In some embodiments, the organic vapor comprises a carboxylic acid. In some embodiments, the organic vapor comprises trifluoroacetic acid. In some embodiments, the organic vapor comprises trifluoroacetic anhydride, acetic anhydride, trichloroacetic acid, monofluoroacetic acid, difluoroacetic acid, chlorodifluoroacetic acid, thioacetic acid, or thioglycolic acid. In some embodiments, the organic vapor comprises hexafluoroacetylacetone. In some embodiments, the developing chemical comprises a gas phase mixture of a halogenated carboxylic acid and a hydrogen halide. In some embodiments, dry developing the photopatterned metal-containing resist comprises reacting an organic vapor with the photopatterned metal-containing resist to form a volatile compound at a temperature less than about 200° C. In some embodiments, dry developing the photopatterned metal-containing resist comprises exposing the photopatterned metal-containing resist to at least the organic vapor in a plasma-free thermal process. In some embodiments, the photopatterned metal-containing resist is a photopatterned metal-containing EUV resist, and the photopatterned metal-containing EUV resist is an organometallic oxide or an organometallic film. In some embodiments, dry developing the photopatterned metal-containing resist comprises using a development chemistry to selectively remove the EUV-unexposed portions of the resist relative to the EUV-exposed portions to form a resist mask.

[0009] Also provided is a method for removing residue from one or more surfaces of a process chamber, the method including depositing a metal-containing resist material on a surface of a semiconductor substrate in the process chamber, where a portion of the metal-containing resist material forms a residue on the one or more surfaces of the process chamber, and introducing a dry etchant comprising an organic vapor into the process chamber, where the dry etchant at least partially removes the residue on the one or more surfaces of the process chamber.

[0010] In some embodiments, the organic vapor comprises a carboxylic acid. In some embodiments, the organic vapor comprises trifluoroacetic acid. In some embodiments, the organic vapor comprises trifluoroacetic anhydride, acetic anhydride, trichloroacetic acid, monofluoroacetic acid, difluoroacetic acid, chlorodifluoroacetic acid, thioacetic acid, or thioglycolic acid. In some embodiments, the organic vapor comprises hexafluoroacetylacetone. In some embodiments, the dry etchant comprises a gas-phase mixture of a halogenated carboxylic acid and a hydrogen halide. In some embodiments, at least partial removal of the residue comprises reacting the organic vapor with the metal-containing resist material to form a volatile compound at a temperature below about 200° C. In some embodiments, at least partial removal of the residue comprises exposing the organic vapor to at least the metal-containing resist material in a plasma-free thermal process. In some embodiments, the metal-containing resist material is an organometallic oxide or an organometallic-containing film. In some embodiments, the method further includes purging the process chamber after introducing the dry etchant to remove residual dry etchant from the process chamber, and conditioning one or more surfaces of the process chamber by forming a protective coating of a metal-containing resist material on the one or more surfaces of the process chamber. [Brief explanation of the drawings]

[0011] [Figure 1] FIG. 1 is a flow diagram of an exemplary method for depositing and developing photoresist, according to some embodiments.

[0012] [Figure 2] FIG. 2 is a flow diagram of an exemplary method for dry developing a metal-containing resist, according to some embodiments.

[0013] [Figure 3A] FIG. 3A is a cross-sectional schematic view of various processing stages of dry development, according to some embodiments. [Figure 3B] FIG. 3B is a cross-sectional schematic view of various processing stages of dry development, according to some embodiments. [Figure 3C] FIG. 3C is a cross-sectional schematic view of various processing stages of dry development, according to some embodiments.

[0014] [Figure 4A] FIG. 4A is a cross-sectional schematic diagram of dry development without application of an inert gas plasma, according to some embodiments.

[0015] [Figure 4B] FIG. 4B is a cross-sectional schematic diagram of a dry development cycle inert gas plasma for descumming, according to some embodiments.

[0016] [Figure 5] FIG. 5 is a flow diagram of an exemplary method for dry chamber cleaning, according to some embodiments.

[0017] [Figure 6A] 6A-6C are cross-sectional schematic views of various processing stages of dry chamber cleaning, according to some embodiments. [Figure 6B] 6A-6B are cross-sectional schematic views of various processing stages of dry chamber cleaning, according to some embodiments. [Figure 6C] 6A-6C are cross-sectional schematic views of various processing stages of dry chamber cleaning, according to some embodiments. [Figure 6D]6A-6D are cross-sectional schematic views of various processing stages of dry chamber cleaning, according to some embodiments.

[0018] [Figure 7] FIG. 7 is a schematic diagram of an exemplary process station suitable for performing dry development, cleaning, rework, descum, and smoothing operations according to some embodiments.

[0019] [Figure 8] FIG. 8 is a schematic diagram of an exemplary multi-station processing tool suitable for performing the various dry development, cleaning, rework, descum, and smoothing operations described herein.

[0020] [Figure 9] FIG. 9 is a cross-sectional schematic diagram of an exemplary inductively coupled plasma apparatus for carrying out certain embodiments and operations described herein.

[0021] [Figure 10] FIG. 10 is a diagram illustrating a semiconductor process cluster tool architecture having a vacuum integrated deposition and patterning module interfaced with a vacuum transfer module suitable for carrying out the processes described herein.

[0022] [Figure 11A] FIG. 11A is a cross-sectional schematic diagram of an example dry deposition apparatus, according to some embodiments.

[0023] [Figure 11B] FIG. 11B is a detailed cross-sectional side view and plan view of a portion of a top plate, substrate, and edge ring of a dry deposition apparatus, according to some embodiments. DETAILED DESCRIPTION OF THE INVENTION

[0024] The present disclosure relates generally to the field of semiconductor processing. In certain aspects, the present disclosure is directed to processes and apparatus for developing photoresists (e.g., EUV-sensitive metal- and / or metal oxide-containing photoresists) using organic vapors, such as organic acids, to form patterning masks, for example, in EUV patterning or other wavelength patterning situations. While the following description focuses on EUV photoresists, it will be apparent that the photoresists described herein may be suitable for use with other wavelengths of radiation, and the techniques and apparatus described herein are not limited solely to the production of EUV photoresists.

[0025] Reference will be made in detail herein to specific embodiments of the present disclosure. Examples of specific embodiments are illustrated in the accompanying drawings. While the present disclosure will be described in conjunction with these specific embodiments, it will be understood that it is not intended to limit the disclosure to such specific embodiments. On the contrary, it is intended to cover alternatives, modifications, and equivalents that may be included within the spirit and scope of the present disclosure. In the following description, numerous specific details are set forth in order to provide a thorough understanding of the present disclosure. The present disclosure may be practiced without some or all of these specific details. In other instances, well-known process operations have not been described in detail so as not to unnecessarily obscure the present disclosure.

[0026] Introduction Patterning thin films in semiconductor processing is often a critical step in semiconductor manufacturing. Patterning involves lithography. In traditional photolithography, such as 193 nm photolithography, patterns are printed by emitting photons from a photon source onto a mask and printing the pattern onto a light-sensitive photoresist, which causes a chemical reaction within the photoresist that, after development, removes certain portions of the photoresist to form the pattern.

[0027] Advanced technology nodes (as defined by the International Technology Roadmap for Semiconductors) include the 22 nm, 16 nm, and beyond. For example, at the 16 nm node, the width of a typical via or line in a damascene structure is typically about 30 nm or less. The scaling of features on advanced semiconductor integrated circuits (ICs) and other devices drives lithography to improve resolution.

[0028] Extreme ultraviolet (EUV) lithography can extend lithography technology by moving to shorter imaging source wavelengths than are achievable with traditional photolithography methods. EUV sources with wavelengths of approximately 10-20 nm, or even 11-14 nm, e.g., 13.5 nm, can be used in cutting-edge lithography tools, also known as scanners. EUV radiation is strongly absorbed by a wide range of solid and fluid materials, including quartz and water vapor, and therefore operates in a vacuum.

[0029] EUV lithography utilizes an EUV resist that is patterned to form a mask used to etch the underlying layer. The EUV resist may be a polymer-based chemically amplified resist (CAR) obtained by a liquid-based spin-on technique. An alternative to CAR is a directly photopatternable metal oxide-containing film, such as those available from Inpria, Corvallis, Oregon, and described in U.S. Patent Application Publication Nos. 2017 / 0102612, 2016 / 021660, and 2016 / 0116839, which are incorporated herein by reference at least for their disclosure of photopatternable metal oxide-containing films. Such films may be obtained by spin-on techniques or dry vapor deposition. Metal oxide-containing films can be patterned directly (i.e., without the use of a separate photoresist) by EUV exposure in a vacuum atmosphere providing patterning resolution of less than 30 nm, as described, for example, in U.S. Pat. No. 9,996,004, issued June 12, 2018, and entitled "EUV PHOTOPATTERNING OF VAPOR-DEPOSITED METAL OXIDE-CONTAINING HARD MASKS," and / or International Patent Application No. PCT / US2019 / 31618, filed May 9, 2019, and entitled "METHODS FOR MAKING EUV PATTERNABLE HARD MASKS," the disclosures of which, at least relating to the composition, deposition, and patterning of directly photopatternable metal oxide films to form EUV resist masks, are incorporated herein by reference. Generally, patterning involves exposing an EUV resist to EUV radiation to form a photopattern in the resist, followed by development to remove portions of the resist according to the photopattern and form the mask.

[0030] While this disclosure relates to lithographic patterning techniques and materials exemplified by EUV lithography, it should also be understood that it is applicable to other next-generation lithography techniques. In addition to EUV, which includes the standard 13.5 nm EUV wavelength currently in use and under development, the most relevant radiation sources for such lithography are DUV (deep UV), which generally refers to the use of 248 nm or 193 nm excimer laser sources; X-ray, formally including EUV in the lower energy range of the X-ray range; and e-beam, which can cover a wide energy range. Specific methods may depend on the specific materials and applications used in the semiconductor substrate and final semiconductor device. Therefore, the methods described in this application are merely exemplary of methods and materials that may be used in the present technology.

[0031] Directly photopatternable EUV resists can be composed of or contain metals and / or metal oxides mixed within organic components. Metals / metal oxides hold great promise in that they can enhance EUV photon absorption, generate secondary electrons, and / or exhibit high etch selectivity relative to underlying film stacks and device layers. To date, these resists have been developed using wet (solvent) approaches, which require wafers to be transferred to a track where they are exposed to a developing solvent, dried, and baked. Wet development not only limits productivity but can also cause line collapse due to surface tension effects and / or delamination.

[0032] Dry development techniques have been proposed to overcome these problems by eliminating substrate delamination and interfacial defects. Dry development can improve performance at narrower line widths (e.g., by preventing the surface tension-induced line collapse and delamination seen with wet development) and potentially increase throughput (e.g., by avoiding the need for wet development tracks). Other advantages may include the elimination of the use of organic solvent developers, reduced sensitivity to underlayer adhesion, and elimination of solubility-based limitations. Dry development offers additional tunability and is also capable of critical dimension (CD) control and scum removal.

[0033] Dry development presents its own challenges, including etch selectivity between unexposed and EUV-exposed resist materials, which can result in higher dose to size requirements for effective resist exposure when compared to wet development. Suboptimal selectivity can also result in PR corner rounding due to reduced contrast at the feature edge, which can increase line CD variability in the subsequent transfer etch step.

[0034] Dry removal of metal-containing resist According to various aspects of the present disclosure, a photopatterned metal-containing photoresist is developed by exposure to a vapor of an organic acid or other gas-phase precursor. An EUV-sensitive metal or metal oxide-containing film, such as an organotin oxide, is disposed on a semiconductor substrate. The EUV-sensitive metal or metal oxide-containing film is directly patterned by EUV exposure in a vacuum atmosphere. The pattern is then developed using a development chemical to form a resist mask. In some embodiments, the development chemical is a dry development chemical. In some embodiments, the dry development chemical includes an organic vapor, such as trifluoroacetic acid. Such dry development techniques can be performed using either a gentle plasma (high pressure, low power) or a non-plasma thermal process while flowing the organic vapor. Additionally or alternatively, the present disclosure provides dry chamber cleaning of EUV resist material or metal-containing resist material from the interior surfaces of a process chamber by exposure to an organic acid or other gas-phase precursor. In some embodiments, the organic vapor is trifluoroacetic acid. The dry cleaning can also be a non-plasma thermal-based cleaning operation. Dry chamber cleaning can be performed in any process chamber used for deposition, bevel edge and / or backside cleaning, bake, develop, or etch operations.

[0035] Various embodiments of the present disclosure can include combining all dry operations with vapor deposition, EUV lithography patterning, and dry development. Various other embodiments include a combination of wet and dry processing operations, for example, spin-on EUV photoresist (a wet process) can be combined with dry development or other wet or dry processes as described herein. Also described are various post-deposition (or post-application) processes such as bevel and backside cleaning, chamber cleaning, descumming, smoothing, curing to modify and enhance film properties, and photoresist rework processes.

[0036] FIG. 1 shows a flow diagram of an exemplary method for depositing and developing photoresist, according to some embodiments. The operations of process 100 may be performed in a different order and / or with different, fewer, or additional operations. Aspects of process 100 may be described with reference to FIGS. 2, 3A-3C, 4A-4B, 5, and 6A-6D. One or more operations of process 100 may be performed using an apparatus described in any one of FIGS. 7-11B. In some embodiments, the operations of process 100 may be implemented, at least in part, according to software stored on one or more non-transitory computer-readable media. In some embodiments, a dry chamber clean may be performed after deposition, backside clean and bevel edge clean, post-apply bake, post-exposure bake, or dry develop.

[0037] In block 102 of process 100, a layer of photoresist is deposited. This can be either a dry deposition process, such as a vapor deposition process, or a wet process, such as a spin-on deposition process.

[0038] The photoresist may be a metal-containing EUV resist. The EUV-sensitive metal or metal oxide-containing film may be deposited on a semiconductor substrate by any suitable technique, including wet (e.g., spin-on) or dry (e.g., CVD) deposition techniques. For example, the described process is demonstrated for organotin oxide-based EUV photoresist compositions, and is applicable to both commercially available spin-coatable formulations (e.g., formulations available from Inpria Corp., Corvallis, Oregon) and formulations applied using dry vacuum deposition techniques, as further described below.

[0039] The semiconductor substrate can include any material structure suitable for photolithography processing, particularly for the production of integrated circuits and other semiconductor devices. In some embodiments, the semiconductor substrate is a silicon wafer. The semiconductor substrate may be a silicon wafer having features ("underlying features") formed thereon that have an irregular surface topography. As referred to herein, a "surface" is the surface onto which a film of the present disclosure is deposited or the surface that is exposed to EUV during processing. The underlying features may include areas from which material has been removed (e.g., by etching) or areas to which material has been added (e.g., by deposition) during processing prior to performing the method of the present disclosure. Such pre-processing may include the method of the present disclosure or other processing methods in an iterative process in which two or more layers of features are formed on the substrate.

[0040] EUV-sensitive thin films can be deposited on semiconductor substrates, and such films can act as resists for subsequent EUV lithography and processing. Such EUV-sensitive thin films include materials that, upon exposure to EUV, undergo changes such as the loss of bulky pendant substituents attached to metal atoms in low-density M-OH-rich materials, allowing crosslinking to a higher-density MOM-bonded metal oxide material. Through EUV patterning, regions of the film are formed that have altered physical or chemical properties compared to unexposed regions. These properties can be exploited in subsequent processing, such as to dissolve either the unexposed or exposed regions, or to selectively deposit materials in either the exposed or unexposed regions. In some embodiments, the unexposed film has a more hydrophobic surface than the exposed film under the conditions under which such subsequent processing is performed. For example, material removal may be achieved by exploiting differences in the film's chemical composition, density, and crosslinking. Removal can be achieved by wet or dry processes, as further described below.

[0041] In various embodiments, the thin film is an organometallic material, such as an organotin material including tin oxide, or other metal oxide material / moiety. The organometallic compound can be made by the vapor-phase reaction of an organometallic precursor with a reverse reactant. In various embodiments, the organometallic compound is formed by mixing a specific combination of organometallic precursors having bulky alkyl or fluoroalkyl groups with a reverse reactant and polymerizing the mixture in the vapor phase to generate a low-density EUV-sensitive material that deposits on the semiconductor substrate.

[0042] In various embodiments, the organometallic precursors contain at least one alkyl group on each metal atom that can survive the gas phase reaction, but other ligands or ions coordinated to the metal atom can be replaced by counter-reactants. The organometallic precursors include those of the formula: M a R b L c (Formula 1)

[0043] where M is an element with a high patterning radiation absorption cross section and R is C n H 2n+1 and the like, preferably n=1-6, L is a ligand, ion, or other moiety that reacts with the reverse reactant, and a≧1, b≧1, and c≧1. In various embodiments, M is 1×10 7 cm 2 M may be, for example, selected from the group consisting of tin, hafnium, tellurium, bismuth, indium, antimony, iodine, germanium, and combinations thereof. In some embodiments, M is tin. R may be, for example, a compound of the formula C n F x H (2n+1)In various embodiments, R has at least one beta hydrogen or beta fluorine. For example, R can be selected from the group consisting of methyl, ethyl, i-propyl, n-propyl, t-butyl, i-butyl, n-butyl, sec-butyl, n-pentyl, i-pentyl, t-pentyl, sec-pentyl, and mixtures thereof. L can be any moiety that is readily displaced by a reverse reactant to produce an M-OH moiety, such as a moiety selected from the group consisting of an amine (dialkylamino, monoalkylamino, etc.), an alkoxy, a carboxylate, a halogen, and mixtures thereof.

[0044] The organometallic precursor may be any of a wide variety of candidate metal organic precursors. For example, when M is tin, such precursors include t-butyltris(dimethylamino)tin, i-butyltris(dimethylamino)tin, n-butyltris(dimethylamino)tin, sec-butyltris(dimethylamino)tin, i-propyl(tris)dimethylaminotin, n-propyltris(dimethylamino)tin, ethyltris(dimethylamino)tin, and similar alkyl(tris)(t-butoxy)tin compounds, such as t-butyltris(t-butoxy)tin. In some embodiments, the organometallic precursor is partially fluorinated.

[0045] The reverse reactant has the ability to replace a reactive moiety, ligand, or ion (e.g., L in Formula 1 above) to link at least two metal atoms via a chemical bond. Reverse reactants can include water, peroxides (e.g., hydrogen peroxide), dihydroxy or polyhydroxy alcohols, fluorinated dihydroxy or polyhydroxy alcohols, fluorinated glycols, and other sources of hydroxyl moieties. In various embodiments, the reverse reactant reacts with the organometallic precursor by forming oxygen bridges between adjacent metal atoms. Other potential reverse reactants include hydrogen sulfide and hydrogen disulfide, which can bridge metal atoms via sulfur bridges.

[0046] In addition to the organometallic precursor and back-reactant, the thin film can include optional materials to modify the film's chemical or physical properties, such as to modify its sensitivity to EUV or to enhance its etch resistance. Such optional materials may be introduced, such as by doping during vapor formation, before deposition on the semiconductor substrate, after deposition of the thin film, or both. In some embodiments, the introduction of a mild remote H plasma can replace some Sn-L bonds with Sn-H, thereby enhancing the reactivity of the resist under EUV.

[0047] In various embodiments, EUV patternable films are prepared and deposited on semiconductor substrates using vapor deposition equipment and processes known in the art. In such processes, polymerized organometallic materials are formed in the vapor phase or in situ on the surface of the semiconductor substrate. Suitable processes include, for example, chemical vapor deposition (CVD), atomic layer deposition (ALD), and ALD using CVD components, such as discontinuous ALD-like processes in which the metal precursor and the counter-reactant are separated in time or space.

[0048] In general, the method includes mixing a vapor flow of an organometallic precursor with a vapor flow of a reverse reactant to form a polymerized organometallic material and depositing the organometallic material on a surface of a semiconductor substrate. In some embodiments, multiple organometallic precursors are included in the vapor flow. In some embodiments, multiple reverse reactants are included in the vapor flow. As will be appreciated by those skilled in the art, the mixing and deposition aspects of the process can occur simultaneously in a substantially continuous process.

[0049] In an exemplary continuous CVD process, two or more gas streams of a source of organometallic precursor and a reverse reactant are introduced into a deposition chamber of a CVD apparatus via separate inlet paths, where they mix and react in the gas phase to form a cohesive polymeric material (e.g., via metal-oxygen-metal bond formation). The gas streams can be introduced, for example, using separate injection inlets or a dual plenum showerhead. The apparatus is configured so that the flows of organometallic precursor and reverse reactant mix within the chamber, allowing them to react and form a polymerized organometallic material. Without limiting the mechanism, function, or utility of the present technology, it is believed that the product from such a gas-phase reaction becomes heavier in molecular weight as metal atoms are crosslinked by the reverse reactant, and is then condensed or, in some cases, deposited onto a semiconductor substrate. In various embodiments, the steric hindrance of the bulky alkyl groups prevents the formation of a densely packed network, resulting in a smooth, amorphous, low-density film.

[0050] CVD processes are typically performed at reduced pressures, such as 10 milliTorr to 10 Torr. In some embodiments, the process is performed at 0.5 to 2 Torr. In some embodiments, the temperature of the semiconductor substrate is equal to or less than the temperature of the reactant stream. For example, the substrate temperature can be between 0°C and 250°C, or between ambient temperature (e.g., 23°C) and 150°C. In various processes, deposition of the polymerized organometallic material onto the substrate occurs at a rate that is inversely proportional to the surface temperature.

[0051] In some embodiments, the EUV patternable film is fabricated and deposited on the semiconductor substrate using wet deposition equipment and processes known in the art, for example, an organometallic material is formed on the surface of the semiconductor substrate by spin coating.

[0052] The thickness of the EUV-patternable film formed on the surface of a semiconductor substrate can vary depending on the surface characteristics, materials used, and processing conditions. In various embodiments, the film thickness can range from 0.5 nm to 100 nm and can be thick enough to absorb a majority of the EUV light under EUV patterning conditions. EUV-patternable films can support absorption of 30% or more, thereby resulting in significantly fewer EUV photons available toward the bottom of the EUV-patternable film. High EUV absorption results in more crosslinking and densification near the top of the EUV-exposed film compared to the bottom of the EUV-exposed film. Insufficient crosslinking can make the resist more susceptible to lift-off or disintegration in wet development, whereas dry development does not present such a risk. All-dry lithography techniques can facilitate more efficient utilization of EUV photons with more opaque resist films. While efficient utilization of EUV photons can occur with EUV-patternable films with higher overall absorption, it will be understood that in some cases, EUV-patternable films may have less than about 30% absorption. For comparison, most other resist films have a maximum overall absorption of less than 30% (e.g., 10% or less, or 5% or less), thereby ensuring sufficient exposure of the resist material at the bottom of the resist film. In some embodiments, the film thickness is 10 nm to 40 nm, or 10 nm to 20 nm. Without limiting the mechanism, function, or utility of the present disclosure, the disclosed process has few limitations on the surface adhesion properties of the substrate and can therefore be applied to a wide variety of substrates. Furthermore, as discussed above, the deposited film can closely conform to surface features without "filling" or planarizing such features, which can provide advantages when forming a mask over a substrate, such as a substrate with underlying features.

[0053] In addition to depositing a thin metal-containing EUV resist film on a semiconductor substrate in block 102 of process 100, some metal-containing EUV resist material may form as residue on the interior surfaces of the process chamber. The interior surfaces may include the chamber walls, floor, and ceiling of the process chamber. Other interior surfaces may include the showerhead, nozzle, and substrate support surface. The metal-containing EUV resist material may form as a result of a dry deposition process, such as a CVD or ALD process. The thickness of the metal-containing EUV resist material residue may increase over time as a result of additional processing (e.g., deposition) operations performed in the process chamber. The residue tends to flake off, shed particles, or peel from the interior surfaces of the process chamber, causing contamination in downstream processes.

[0054] In block 150 of process 100, a dry chamber clean is performed after the deposition of the metal-containing EUV resist film in block 102 of process 100. This allows the deposition and dry clean to be performed in the same process chamber. However, it will be understood that the dry chamber clean may, in some embodiments, be performed in a different process chamber than the deposition operation. Indeed, a dry chamber clean may be performed after a bevel edge and / or backside clean, bake, develop, or etch operation, since residues may also form in the chamber in which any of these operations are performed, which may or may not be the same as the deposition chamber.

[0055] The dry-deposited EUV resist materials being removed are typically composed of Sn, O, and C, but the same cleaning techniques can be extended to films of other metal oxide resists and materials. Additionally, this technique can be used for film stripping and photoresist rework.

[0056] In block 104, an optional cleaning process is performed to clean the backside and / or bevel edge of the semiconductor substrate. Backside and / or bevel edge cleaning can non-selectively etch the EUV resist film and evenly remove films with various levels of oxidation or crosslinking on the substrate backside and bevel edge. During the application of EUV-patternable films by wet or dry deposition processes, unintended deposition of resist material can occur on the bevel edge and / or backside of the substrate. This unintended deposition can subsequently result in unwanted particles migrating to the top surface of the semiconductor substrate, resulting in particle defects. Furthermore, this bevel edge and backside deposition can also cause downstream processing issues, including contamination of patterning (scanner) and development tools. Traditionally, this bevel edge removal and backside deposition is accomplished by wet cleaning techniques. For spin-coated photoresist materials, this process, called edge bead removal (EBR), is performed by directing a flow of solvent from above and below the bevel edge while the substrate is spinning. The same process can be applied to soluble organic tin oxide based resists deposited by vapor deposition techniques.

[0057] The bevel edge and / or backside cleaning of the substrate may be a dry cleaning process. In some embodiments, the dry cleaning process involves vapor and / or plasma having one or more of the following gases: HBr, HCl, BCl3, SOCl2, Cl2, BBr3, H2, O2, PCl3, CH4, methanol, ammonia, formic acid, NF3, and HF. In some embodiments, the dry cleaning process may use the same chemistries as the dry development process described herein. For example, organic acids such as trifluoroacetic acid or other organic vapors may be used for bevel edge and / or backside cleaning. For bevel edge and / or backside cleaning processes, the vapor and / or plasma must be limited to specific areas of the substrate to ensure that only the backside and bevel are removed without degrading the film on the front side of the substrate.

[0058] Process conditions can be optimized for bevel edge and / or backside cleaning. In some embodiments, higher temperatures, higher pressures, and / or higher reactant flow rates can increase the etch rate. Suitable process conditions for dry bevel edge and backside cleaning can be as follows: reactant flow rates of 100-10,000 sccm (e.g., 500 sccm of HCl, HBr, HI, or H2 and Cl2 or Br2, BCl3, or H2, or other halogen-containing compounds), depending on the photoresist film and composition and properties; temperature of 20-140°C (e.g., 80°C); pressure of 20-1,000 mTorr (e.g., 100 mTorr), or pressure of 50-765 Torr (e.g., 760 Torr); plasma power of 0-500 W at radio frequency (e.g., 13.56 MHz); and duration of about 10-20 seconds, depending on the photoresist film and composition and properties. Bevel and / or backside cleaning can be accomplished using a Coronus® tool available from Lam Research, Inc., Fremont, California, although a wider range of process conditions can be used depending on the capabilities of the processing reactor.

[0059] Bevel edge and / or backside cleaning can alternatively be extended to a complete photoresist removal or photoresist “rework,” in which the applied EUV photoresist is removed and the semiconductor substrate is prepared for reapplication of photoresist, such as if the original photoresist is damaged or otherwise defective. Because photoresist rework should be accomplished without damaging the underlying semiconductor substrate, oxygen-based etching should be avoided. Instead, organic vapor chemistries or variations of halogen-containing chemistries, as described herein, can be used. It will be understood that the photoresist rework operation can be applied at any stage during process 100. Thus, the photoresist rework operation can be applied after deposition, after bevel edge and / or backside cleaning, after PAB processing, after EUV exposure, after PEB processing, after development, or after a hard bake. In some embodiments, photoresist rework may be performed to non-selectively remove exposed and unexposed regions of the photoresist, but selectively with respect to the underlying layer.

[0060] In some embodiments, the photoresist rework process involves vapor and / or plasma with one or more of the following gases: HBr, HCl, HI, BCl3, Cl2, BBr3, H2, PCl3, CH4, methanol, ammonia, formic acid, NF3, HF. In some embodiments, the photoresist rework can use the same chemistries as the dry development process described herein. For example, the photoresist rework can use organic acids such as trifluoroacetic acid or other organic vapors.

[0061] Process conditions can be optimized for photoresist rework. In some embodiments, higher temperatures, higher pressures, and / or higher reactant flow rates can increase the etch rate. Suitable process conditions for photoresist rework can be as follows: reactant flow rates of 100-500 sccm (e.g., 500 sccm of HCl, HBr, HI, BCl3 or H2 and Cl2 or Br2), depending on the photoresist film and composition and properties; temperature of 20-140°C (e.g., 80°C); pressure of 20-1000 mTorr (e.g., 300 mTorr), or pressure of 50-765 Torr (e.g., 760 Torr); plasma power of 0-800 W (e.g., 500 W) at high frequency (e.g., 13.56 MHz); and 0-200 V. b (The harder the underlying substrate material, the higher the bias that can be used), and a time of about 20 seconds to 3 minutes, sufficient to completely remove the EUV photoresist. These conditions are suitable for some process reactors, for example, the Kiyo etch tool available from Lam Research, Inc., Fremont, California, but it should be understood that a wider range of process conditions can be used depending on the capabilities of the process reactor.

[0062] In block 150 of process 100, a dry chamber clean operation may be performed after the bevel edge and / or backside clean in block 104 of process 100. This allows the bevel edge and / or backside clean and the dry chamber clean to be performed in the same process chamber. However, it will be understood that the dry chamber clean may be performed in a different process chamber than the bevel edge and / or backside clean in some embodiments.

[0063] In block 106 of process 100, an optional post-apply bake (PAB) is performed after deposition of the metal-containing EUV resist film and before EUV exposure. The PAB process can involve a combination of thermal treatment, chemical exposure, and moisture to increase the EUV sensitivity of the metal-containing EUV resist film, thereby reducing the EUV dose and developing a pattern in the metal-containing EUV resist film. The PAB process temperature can be adjusted and optimized to increase the sensitivity of the metal-containing EUV resist film. For example, the process temperature can be about 90°C to about 200°C, or about 150°C to about 190°C. In some embodiments, the PAB process can be performed at a pressure between atmospheric pressure and vacuum for a process period of about 1 to 15 minutes, e.g., about 2 minutes. In some embodiments, the PAB process can be performed at a temperature of about 100°C to 230°C for about 1 to 2 minutes.

[0064] In block 150 of process 100, a dry chamber clean operation may be performed after the PAB process in block 106 of process 100. This allows the bake and dry chamber clean to be performed in the same process chamber. However, it will be understood that the dry chamber clean may be performed in a different process chamber than the PAB process in some embodiments.

[0065] In block 108 of process 100, the metal-containing EUV resist film is exposed to EUV radiation to develop the pattern. Generally speaking, the EUV exposure causes changes in chemical composition and crosslinking in the metal-containing EUV resist film, resulting in etch selectivity contrast that can be exploited in subsequent development.

[0066] The metal-containing EUV resist film can then be patterned by exposing regions of the film to EUV light, typically under relatively high vacuum. EUV devices and imaging methods useful herein include those known in the art. In particular, as described above, exposed regions of the film are formed by EUV patterning with altered physical or chemical properties compared to unexposed regions. For example, in exposed regions, cleavage of metal-carbon bonds can occur via beta-hydride elimination, leaving reactive and accessible metal hydride functional groups that can be converted to hydroxides and bridging metal oxide moieties via metal-oxygen bridges during a subsequent post-exposure bake (PEB) step. This process can be used to create chemical contrast for development as a negative resist. Generally, the higher the number of beta-H groups in the alkyl group, the more sensitive the film. This can also be described as weaker Sn-C bonds with more branching. Following exposure, baking the metal-containing EUV resist film can result in further crosslinking of the metal oxide film. The difference in properties between the exposed and unexposed regions can be exploited in subsequent processing, such as dissolving the unexposed regions or depositing material in the exposed regions. For example, the pattern can be developed using dry methods to form a metal oxide-containing mask.

[0067] In particular, in various embodiments, hydrocarbyl-terminated tin oxide present on the surface is converted to hydrogen-terminated tin oxide in the exposed regions of the imaging layer, especially when the exposure is carried out in a vacuum using EUV. However, removing the exposed imaging layer from vacuum to air or by the controlled introduction of oxygen, ozone, HO, or water can oxidize the surface Sn-H to Sn-OH. The difference in properties between the exposed and unexposed regions can be exploited in subsequent processing, for example, by reacting the irradiated regions, the unirradiated regions, or both, with one or more reagents to selectively add or remove material from the imaging layer.

[0068] Without limiting the mechanism, function, or utility of the present technology, for example, 10 mJ / cm 2 ~100mJ / cm 2 EUV exposure at doses of 1000 nm leads to the cleavage of Sn-C bonds, which results in the loss of alkyl substituents, relieves steric hindrance, and allows the low-density film to collapse. In addition, the reactive metal-H bonds generated in the beta-hydride elimination reaction can react with neighboring active groups, such as hydroxyls, in the film, which can lead to further crosslinking and densification, creating chemical contrast between exposed and unexposed regions.

[0069] After exposing the metal-containing EUV resist film to EUV light, a photopatterned metal-containing EUV resist is provided, which includes EUV-exposed regions and EUV-unexposed regions.

[0070] At block 110 of process 100, an optional post-exposure bake (PEB) is performed to further enhance the etch selectivity contrast of the photopatterned metal-containing EUV resist. The photopatterned metal-containing EUV resist can be thermally treated in the presence of various chemical species to promote crosslinking of the EUV-exposed regions, or can simply be baked on a hotplate in ambient air, for example, at 100°C to 250°C for 1 to 5 minutes (e.g., 190°C for 2 minutes).

[0071] In various embodiments, the bake strategy involves careful control of the bake atmosphere, the introduction of reactive gases, and / or the rate of increase in bake temperature. Examples of useful reactive gases include, for example, air, HO, HO vapor, CO, CO, O, O, CH, CHOH, N, H, NH, NO, NO, alcohol, acetylacetone, formic acid, Ar, He, or mixtures thereof. The PEB process is designed to (1) drive complete evaporation of organic fragments generated during EUV exposure, (2) oxidize any Sn-H, Sn-Sn, or Sn radical species generated by EUV exposure to metal hydroxides, and (3) promote crosslinking between adjacent Sn-OH groups to form a more densely crosslinked SnO-like network. The bake temperature is carefully selected to achieve optimal EUV lithography performance. A PEB temperature that is too low can result in insufficient crosslinking, resulting in reduced chemical contrast for development at a given dose. Too high a PEB temperature can also result in adverse effects such as severe oxidation and film shrinkage in unexposed areas (in this example, areas removed by development of the patterned film to form the mask) and undesirable interdiffusion at the interface between the photopatterned metal-containing EUV resist and the underlayer, both of which can contribute to loss of chemical contrast due to insoluble scum and increased defect density. The PEB treatment temperature can be about 100°C to about 300°C, about 170°C to about 290°C, or about 200°C to about 240°C. In some embodiments, the PEB treatment can be performed at a pressure between atmospheric and vacuum for a treatment period of about 1 to 15 minutes, e.g., about 2 minutes. In some embodiments, the PEB thermal treatment can be repeated to further enhance etch selectivity.

[0072] In block 150 of process 100, a dry chamber clean operation may be performed after the PEB process in block 110 of process 100. This allows the bake and dry chamber clean to be performed in the same process chamber. However, it will be understood that the dry chamber clean may be performed in a different process chamber than the PEB process in some implementations.

[0073] At block 112 of process 100, the photopatterned metal-containing EUV resist is developed to form a resist mask. In various embodiments, either the exposed regions are removed (positive tone) or the unexposed regions are removed (negative tone). In some embodiments, development can include selective deposition of the photopatterned metal-containing EUV resist onto either the exposed or unexposed regions, followed by an etching operation. In some embodiments, development can be performed by exposure to one or more organic vapors (e.g., trifluoroacetic acid). Development can be performed without applying a plasma in some embodiments. Alternatively, development can be performed by a flow of one or more organic vapors (e.g., trifluoroacetic acid) activated in a remote plasma source or by exposure to remote UV radiation. The photoresist for development can include an element selected from the group consisting of tin, hafnium, tellurium, bismuth, indium, antimony, iodine, and germanium. The element can have a high patterning radiation absorption cross section. In some embodiments, the element can have a high EUV absorption cross section. In some embodiments, metal-containing EUV resists can have an overall absorption of greater than 30%, which in all-dry lithography processes allows for more efficient utilization of EUV photons and allows for the development of thicker and more EUV-opaque resists.

[0074] An example of a development process involves subjecting an organotin oxide-containing EUV-sensitive photoresist thin film (e.g., 10-30 nm thick, e.g., 20 nm thick) to an EUV exposure dose and post-exposure bake, followed by development. The photoresist film may be deposited based on the gas-phase reaction of an organotin precursor, such as isopropyl(tris)(dimethylamino)tin, with water vapor, or may be a spin-on film containing tin clusters in an organic matrix.

[0075] In block 150 of process 100, a dry chamber clean may be performed after the dry development in block 112 of process 100. This allows the dry development and dry chamber clean to be performed in the same process chamber. However, it will be understood that the dry chamber clean may be performed in a different process chamber than the dry development in some embodiments. Furthermore, it will be understood that the dry chamber clean may be performed in the same process chamber as the etching operation or in a different process chamber. The etching operation may be applied to etch an underlying substrate layer of the semiconductor substrate.

[0076] In block 114 of process 100, the semiconductor substrate optionally undergoes a hard bake. During the hard bake, the semiconductor substrate is exposed to high temperatures. For example, the semiconductor substrate may be exposed to temperatures of about 50° C. or higher, about 100° C. to about 300° C., or about 170° C. to about 290° C. The hard bake can drive off residual solvents or etching gases from development.

[0077] FIG. 2 shows a flow diagram of an exemplary method for dry developing a metal-containing resist, according to some embodiments. The operations of process 200 may be performed in a different order and / or with a different, fewer, or additional number of operations. Aspects of process 200 may be described with reference to FIGS. 3A-3C and 4A-4B. One or more operations of process 200 may be performed using an apparatus described in any one of FIGS. 7-11B. In some embodiments, the operations of process 200 may be implemented, at least in part, according to software stored on one or more non-transitory computer-readable media.

[0078] In block 202 of process 200, a photopatterned metal-containing resist is provided on a surface of a semiconductor substrate in a process chamber. The metal-containing resist may be deposited on the surface of the semiconductor substrate. The metal-containing resist may be exposed to UV radiation (e.g., EUV radiation) by a scanner or an EUV lithography tool to form the photopatterned metal-containing resist. In some implementations, the photopatterned metal-containing resist is a photopatterned metal-containing EUV resist. For example, the photopatterned metal-containing EUV resist is an organometallic oxide or organometallic film. The semiconductor substrate may be provided in the process chamber after processing in the scanner and / or PEB processing chamber.

[0079] In block 204 of process 200, the photopatterned metal-containing resist is dry-developed by exposing it to a developer chemical containing an organic vapor to selectively remove portions of the resist and form a resist mask. Dry-developing the photopatterned metal-containing resist involves using the developer chemical to selectively remove portions of the resist not exposed to EUV light relative to the EUV-exposed portions to form a resist mask. Typically, development is performed using wet developer chemicals. Wet development using solvents generates undesirable waste streams. Wet development generally involves moisture and / or oxygen, which more easily leads to scum formation. While wet development is limited by solubility and cluster size, dry development is not. Wet development is more prone to pattern collapse and delamination issues that dry development avoids. Development in the present disclosure is performed in the gas phase using dry developer chemicals instead of wet developer chemicals.

[0080] Development using dry development chemistries typically involves halogen vapors, such as boron trichloride (BCl3) vapor, hydrogen gas (H2) mixed with chlorine gas (Cl2) or bromine gas (Br2), or hydrogen halide vapors, such as hydrogen bromide (HBr), hydrogen chloride (HCl), or hydrogen fluoride (HF). However, such vapors can leave residue or scum after development. The residues can include residual etch by-products adsorbed on the semiconductor substrate surface and, in some cases, on the chamber walls. For example, halogen vapors can react with moisture or oxygen to form residual etch by-products that are difficult to remove. In some cases, residual etch by-products include bromides, which are sticky and difficult to remove. The accumulation of residual etch by-products can cause process drift, resulting in the use of dangerous precautions in the process chamber. Furthermore, residues adsorbed on the semiconductor substrate can desorb from the semiconductor substrate and contaminate downstream processing tools. In some cases, the residues can contain high concentrations of metal or metal oxide clusters, which can contaminate downstream processing tools. Additionally, residual etch byproducts are difficult to remove and do not readily volatilize, which may require a separate plasma step or a separate chamber with plasma capabilities, which would otherwise result in high temperature swings that volatilize the residues, which is often undesirable for the semiconductor substrate and process chamber.

[0081] The developer chemical of the present disclosure is an organic vapor. The organic vapor may be an organic acid. In some embodiments, the organic acid comprises a carboxylic acid. In some embodiments, the organic acid comprises trifluoroacetic acid (CF3COOH). The organic vapor may be halogenated or at least fluorinated. In some embodiments, the organic vapor comprises hexafluoroacetylacetone (CF3CCH2CCF3). In some embodiments, the organic vapor comprises trifluoroacetic anhydride ((CF3CO)2O), acetic anhydride ((CH3CO)2O), trichloroacetic acid (CCl3COOH), monofluoroacetic acid (CFH2COOH), difluoroacetic acid (CF2HCOOH), mixed halide acetic acids such as chlorodifluoroacetic acid, sulfur-containing analogs of acetic acid, thioacetic acid (CH3COSH), or thioglycolic acid (HSCH2CO2H). In some embodiments, the developer chemical comprises a mixture of a carboxylic acid and a hydrogen halide in the vapor phase. For example, the developer chemical comprises a mixture of acetic acid or formic acid with hydrogen chloride or hydrogen bromide. In some embodiments, the organic vapor may be flowed with or without an inert / carrier gas such as helium (He), neon (Ne), argon (Ar), xenon (Xe), and nitrogen (N2).

[0082] Organic vapors may react with metal-containing resists to form byproducts that are more volatile than those formed from halogen vapors. As an example, etching byproducts of tin bromide can have boiling points of approximately 200°C or higher. However, etching byproducts of tin fluoroacetate can be lower than approximately 200°C. For example, hexatin(II)-di-μ-oxy-octakis-μ-trifluoroacetic acid (1F) is volatile at 191°C at 1 Torr, and tetrakis(trifluoroacetate)tin(IV) (2F) is volatile at 84°C at 1 Torr. Both 1F and 2F offer high thermal stability and volatility. Etching byproducts formed from organic vapors reacting with metal-containing resists can have excellent volatility. In particular, etching byproducts formed from trifluoroacetic acid reacting with EUV-unexposed organometallic resists can have excellent volatility. Without being limited by any theory, trifluoroacetic acid or other fluorinated derivatives of organic acids may increase the volatility of etching byproducts due to their electron-withdrawing effect. Trifluoroacetic acid or other fluorinated derivatives of organic acids can be strong organic acids.

[0083] The organic vapor of the present disclosure may be a strong organic acid. As used herein, a strong organic acid may have a pKa value of about 3.8 or less. The strength of the organic acid may be increased by halogenation. In some embodiments, the strength of the organic acid may be significantly increased by fluorination. For example, while formic acid or acetic acid can etch metal-containing resist materials, such as organometallic resist materials, trifluoroacetic acid can more effectively etch such metal-containing resist materials. While less strong organic acids (e.g., acetic acid) can be plasma-assisted for selective removal of metal-containing resist materials, stronger organic acids can selectively remove metal-containing resist materials without plasma assistance. Thus, in the present disclosure, dry development of metal-containing resists can be performed without plasma assistance. However, as described below, plasma may optionally be used for desorption, descumming, or smoothing operations after dry development. This plasma-based desorption, descumming, or smoothing operation may be unnecessary if the etch byproducts of the organic vapor are volatilized.

[0084] The organic vapors of the present disclosure can be used for dry development in a plasma-free thermal process. This means that dry development can be performed in a process chamber without plasma functionality. In some embodiments, dry development may be performed without a subsequent plasma-based descum or smoothing operation. Eliminating plasma exposure avoids plasma damage to the semiconductor substrate, significantly reducing costs and increasing throughput. Furthermore, the interior surfaces of the process chamber do not need to be resistant to plasma and can be made of materials that are resistant to halogen vapors, such as hydrogen halides. The surfaces of chamber components, such as the chamber walls, ceiling, and showerhead, can be susceptible to corrosion in the presence of moisture and halogen vapors. As a result, the interior surfaces of the process chamber are typically made of materials that are stable in plasma, halogen vapors, and water vapor. However, for the dry development chemistries of the present disclosure, such as trifluoroacetic acid, the interior surfaces of the process chamber of the present disclosure may be made of materials that do not necessarily meet the aforementioned requirements. In some embodiments, the chamber walls of the process chamber may include aluminum oxide, anodized aluminum, or plastic.

[0085] By applying plasma-free thermal techniques, multiple wafers can be batch developed simultaneously in a low-cost thermal vacuum chamber / oven, significantly improving productivity. However, in some embodiments, the thermal dry development process may be followed by exposure to plasma. The subsequent exposure to plasma may be for desorption, descumming, smoothing, or other processing operations.

[0086] Dry development of photopatterned metal-containing resists can be combined with other dry processing operations, such as dry deposition (e.g., CVD) of metal-containing resists. In some embodiments, semiconductor substrate processing may combine all dry steps, including film formation by vapor deposition, EUV lithography patterning, and dry development. Bake operations, bevel edge and / or backside cleaning operations, and chamber cleaning operations may also be dry operations. Such processing operations can avoid the material and production costs associated with wet processing operations, such as wet development. Furthermore, dry processing offers additional tunability, provides greater critical dimension (CD) control, and enables scum removal. Generally, wet processing involves moisture and / or oxygen, which more readily leads to scum formation. While wet development is limited by solubility and cluster size, dry development is not. Wet development is more prone to pattern collapse and delamination issues, which dry development avoids. Additionally, the use of all dry processing operations can facilitate integration within interconnected vacuum processing chambers without exposure to and contamination from ambient air or trace contaminants contained therein. For example, the PEB heat treatment, in which the exposed regions undergo further crosslinking, may occur in the same chamber as development, although it will be understood that the PEB heat treatment may also be performed in a separate chamber.

[0087] In some embodiments, dry development can be performed using a thermal process in conjunction with flowing organic vapors such as trifluoroacetic acid. For example, dry development can be performed in a thermal processing chamber. In some embodiments, the organic vapors such as trifluoroacetic acid can rapidly remove the unexposed portions of the photopatterned metal-containing resist relative to the exposed portions of the photopatterned metal-containing resist, leaving a pattern of the exposed film that can be transferred to an underlying layer of the semiconductor substrate by an etching process.

[0088] In some embodiments, the semiconductor substrate can be exposed to a dry developing chemical, such as a strong organic acid, in a thermal treatment chamber, such as an oven. The thermal treatment chamber can include a developing chemical line for delivering an organic vapor to the thermal treatment chamber. In some embodiments, the thermal treatment chamber can include one or more heating elements for temperature control, such as a heating element coupled to a heating assembly facing the semiconductor substrate in the process chamber for substrate temperature control. In some embodiments, the one or more heating elements can be one or more LEDs. The one or more heaters can heat the semiconductor substrate to a high temperature during dry development to promote volatilization of etching by-products.

[0089] In a thermal dry development process, the photopatterned metal-containing resist is exposed to a development chemistry optimized for etch selectivity between exposed and unexposed regions. Generally, lower temperatures can increase the contrast in etch selectivity, while higher temperatures can decrease the contrast in etch selectivity. Higher temperatures can increase volatilization of etch byproducts and limit residue formation on the semiconductor substrate. In some embodiments, the temperature can be less than about 200°C, between about 20°C and about 190°C, between about 40°C and about 120°C, or between about 50°C and about 100°C. Volatile compounds are formed by reacting the photopatterned metal-containing resist with organic vapors at temperatures below about 200°C.

[0090] The chamber pressure can be adjusted and can affect the etch selectivity between exposed and unexposed regions during thermal dry development. In some embodiments, the chamber pressure can be relatively low and without dilution, and the chamber pressure can be about 0.1 mTorr to about 1000 mTorr, about 0.2 mTorr to about 300 mTorr, or about 0.5 mTorr to about 100 mTorr. In some embodiments, the chamber pressure can be about 20 mTorr to about 2000 mTorr, or about 20 mTorr to about 1000 mTorr, e.g., about 300 mTorr. In some embodiments, the chamber pressure can be relatively high with high flow rates and with dilution, and the chamber pressure can be about 100 Torr to about 765 Torr, or about 200 Torr to about 760 Torr.

[0091] The gas flow rate of the dry development chemistry can be adjusted, and the gas flow can affect the etch selectivity between exposed and unexposed regions during thermal dry development. In some embodiments, the gas flow rate can be about 0.5 SLM to about 30 SLM, about 1 SLM to about 20 SLM, or about 2 SLM to about 15 SLM. The gas flow rate can include the total flow rate of the gases being flowed, including the organic vapor and a carrier gas such as nitrogen or argon. The organic vapor flow rate can be only a portion of the total flow rate, and the organic vapor flow rate can be about 0.01 SLM to about 1 SLM. At higher flow rates, the organic vapor flow rate can be about 1 SLM to about 10 SLM.

[0092] The duration of exposure can be adjusted in the thermal dry development process. The exposure time can depend, among other factors, on the amount of resist desired to be removed, the development chemistry, the amount of crosslinking in the resist, and the composition and properties of the resist. In some embodiments, the duration of exposure can be from about 5 seconds to about 5 minutes, from about 10 seconds to about 3 minutes, or from about 10 seconds to about 1 minute.

[0093] In some embodiments, the photopatterned metal-containing resist is developed using a plasma-free thermal technique. In an alternative embodiment, the photopatterned metal-containing resist is developed using a plasma development process. The photopatterned metal-containing resist is exposed to a development chemistry including radicals / ions of one or more gases. The one or more gases may include organic vapors such as trifluoroacetic acid. The process chamber for processing the semiconductor substrate for dry development may be a plasma generation chamber or may be coupled to a plasma generation chamber separate from the process chamber. The plasma generation chamber may be an inductively coupled plasma (ICP) reactor, a transformer coupled plasma (TCP) reactor, or a capacitively coupled plasma (CCP) reactor using equipment and techniques known in the art. An electromagnetic field acts on one or more gases to generate a plasma in the plasma generation chamber. Ions and / or radicals from the remote plasma may interact with the photopatterned metal-containing resist. The ions and / or radicals may include ions and / or radicals of an organic acid such as trifluoroacetic acid. In some embodiments, a vacuum line may be coupled to the process chamber for pressure control, and a development chemical line may be coupled to the plasma generation chamber for delivering one or more gases to the plasma generation chamber. The process chamber may include one or more heaters for temperature control, such as a heater coupled to a heating assembly facing the substrate for substrate temperature control. In some embodiments, the photopatterned metal-containing resist is developed by exposure to conditions optimized to generate a gentle plasma characterized by high pressure and low power. In some embodiments, the RF power level may be adjusted, and the RF power may be about 1000 W or less, about 800 W or less, or about 500 W or less.

[0094] In addition to or instead of plasma activation, activation of one or more gases in the dry development process can occur by photoactivation. In some embodiments, photoactivation can be achieved by exposure to ultraviolet (UV) radiation. For example, the process chamber may include a lamp, such as a UV lamp, configured to generate UV radiation. Exposing one or more gases to UV radiation can generate radicals of one or more gases that can be used for dry development of the photopatterned metal-containing resist. Exposing the one or more gases to UV radiation can occur without exposing the photopatterned metal-containing resist to UV radiation. In other words, the photopatterned metal-containing resist is invisible to the UV lamp.

[0095] It will be understood that the aforementioned methods of thermal development, plasma development, and photoactivated development may be combined with one another. Such development methods can be applied simultaneously or sequentially. One or more development methods can be applied while flowing dry development chemicals in the gas phase. Development can result in a positive or negative tone, with the dry development chemicals selectively removing either unexposed or exposed material, leaving the exposed or unexposed counterpart as a mask.

[0096] As described above, the etch selectivity during dry development can be adjusted by controlling process conditions such as temperature, pressure, gas flow, gas composition, and plasma power, among other adjustable process conditions. By adjusting the etch selectivity in a single step or multiple steps, desired patterned characteristics can be achieved. In some embodiments, the etch selectivity during dry development is adjusted over one or more steps, thereby affecting the resist profile. More specifically, the amount of taper or re-entrant angle in the resist profile can be controlled by applying dry development chemistries with different etch selectivities over one or more steps. Descumming, photoresist rework, hardening, smoothing, and cleaning operations can also be adjusted according to the adjustable etch selectivity.

[0097] 3A-3C show cross-sectional schematic views of various processing stages of dry development according to some embodiments. The example shown in FIGS. 3A-3C illustrates negative tone dry development. As shown in FIG. 3A, wafer 300 includes substrate 302 and substrate layer 304 to be etched. In some embodiments, substrate layer 304 includes an ashable hard mask such as spin-on carbon (SoC) or other materials, such as silicon, silicon oxide, silicon nitride, or silicon carbide. In some embodiments, substrate layer 304 can be a layer stack disposed on substrate 302. Wafer 300 further includes a photopatterned metal-containing EUV resist film 306. For example, photopatterned metal-containing EUV resist film 306 can be an organometallic layer disposed on substrate layer 304 to be etched. Photopatterned metal-containing EUV resist film 306 can have a thickness of about 5 nm to about 50 nm, or about 10 nm to about 30 nm. The photopatterned metal-containing EUV resist film 306 may be provided in a process chamber after photopatterning in an EUV scanner and / or after the PEB process described above. The photopatterned metal-containing EUV resist film 306 includes a non-EUV-exposed region 306a and an EUV-exposed region 306b. As shown in FIG. 3B, the non-EUV-exposed region 306a of the photopatterned metal-containing EUV resist film 306 can be removed in a dry development process by exposing it to a flow of dry development chemicals without applying a plasma. The dry development chemicals may include organic vapors such as organic acids. The organic acids may include halogenated or fluorinated carboxylic acids. Examples of organic acids include, but are not limited to, trifluoroacetic acid, hexafluoroacetylacetone, trichloroacetic acid, monofluoroacetic acid, and difluoroacetic acid. Other examples of organic acids include mixed halide acetic acids such as chlorodifluoroacetic acid, sulfur-containing analogs of acetic acid, thioacetic acid, and thioglycolic acid. The non-EUV exposed regions 306a are removed after development to form a resist mask 308. The substrate layer 304 to be etched can then be etched using the resist mask 308 to provide the structure illustrated in FIG.

[0098] The organometallic oxide film may have a tetrahedrally coordinated structure. The exposed regions have a higher level of Sn-O-Sn crosslinking, resulting in higher density and lower / slower reactivity with halogenated carboxylic acids. The unexposed regions exhibit lower density due to the presence of bulky alkyl substituents that block access and condensation of Sn-OH moieties. In the unexposed regions, acids such as trifluoroacetic acid more readily protonate the more "basic" and accessible oxygen lone pairs characteristic of more tetrahedrally coordinated organotin oxide hydroxides. Volatile trifluoroacetate by-products are generated and removed from the unexposed regions. Without being limited by any theory, trifluoroacetic acid may selectively protonate the oxygen lone pairs, forming volatile by-products. When the alkyl group is isopropyl, typical EUV patterning doses remove at least two of the three isopropyl substituents, which causes the exposed regions to condense after the PEB step to form a denser, more SnO2-like material, which is less reactive with trifluoroacetic acid due to the adoption of a more hexacoordinated tin structure with less accessibility to oxygen atoms, resulting in a very slow reactivity with trifluoroacetic acid.

[0099] In some cases, residue or scum may remain after development. Residue may result from slow-etching components in less homogeneous EUV resist formulations, including those applied by spin-coating techniques. Such scum may contain high concentrations of metals, which can be problematic during subsequent pattern transfer.

[0100] Additionally or alternatively, after development, roughness may form on the sidewalls of features etched with the developed pattern, some of which may be due to stochastic or non-optimal Gaussian distribution of light, resulting in partially or fully exposed material in areas where the resist should remain unexposed, or vice versa.

[0101] In some embodiments, dry development may be accompanied by a descum / smoothing operation. In some embodiments, the descum and smoothing operation may be an inert gas plasma desorption operation. For example, the inert gas plasma desorption operation may be a helium plasma desorption operation. The inert gas plasma desorption operation may be performed after dry development or may be performed repeatedly with dry development.

[0102] FIG. 4A shows a cross-sectional schematic diagram of dry development without applying an inert gas plasma, according to some embodiments. The photopatterned metal-containing EUV resist film includes exposed and unexposed regions. As shown in FIG. 4A, metal oxide (e.g., SnO x ) particles or clusters may occupy the unexposed areas. As dry development progresses, the metal oxide clusters become more concentrated. Metal oxide clusters are generally difficult to remove. Development may be selective with respect to removing organic materials. After removing the unexposed areas, the metal oxide clusters may remain on the surface of the substrate as scum. Metal oxide clusters remaining on the sidewalls of the exposed areas may cause roughness.

[0103] FIG. 4B shows a cross-sectional schematic diagram of a dry development cycle inert gas plasma for descumming, according to some embodiments. The first stage involves dry development, which removes a substantial portion of the unexposed areas of the photopatterned metal-containing EUV resist film. The dry development chemicals may include, for example, organic acids and / or hydrogen halides. A substantial portion may represent at least more than 70% by volume of the unexposed areas, more than 80% by volume of the unexposed areas, or more than 90% by volume of the unexposed areas. Metal oxide clusters concentrate on the surface of the remaining unexposed areas of the EUV resist film. The second stage involves applying an inert gas plasma, such as helium plasma, at low power and high ion energy for a short period of time. The helium plasma removes the metal oxide clusters. In addition, the helium plasma removes the clusters from the sidewalls and smooths the sidewalls. The helium plasma treatment may also help solidify or harden the patterned EUV resist film, forming a denser metal oxide layer, such as a hard mask. After the helium plasma treatment, a low selectivity dry etch step can be used to remove any residue remaining in the unexposed areas of the EUV resist film.

[0104] In some embodiments, dry development may be repeated with helium plasma treatment for one or more cycles until the unexposed areas of the EUV resist film are removed. Helium plasma descumming / smoothing, as described above, can be repeated with dry development to improve results. In this way, for example, most of the organic components in the unexposed areas of the pattern can be removed by dry development, followed by a short helium plasma operation to remove some of the concentrated metal at the surface, thereby providing access to the remaining underlying organic material, which can be removed in a subsequent dry development operation / cycle. Another cycle of helium plasma can be used to remove the remaining metal, leaving a clean, smooth feature surface. This cycling can continue until all or substantially all scum and roughness residues are removed, leaving a clean, smooth feature surface.

[0105] The process conditions for the descum and smoothing operations can be controlled during or after development. In some embodiments, the reactant flow can be about 50 sccm to about 1000 sccm, or about 100 sccm to about 500 sccm, e.g., about 500 sccm He. In some embodiments, the temperature can be about −60° C. to about 120° C., about −20° C. to about 60° C., or about 20° C. to about 40° C., e.g., about 20° C. In some embodiments, the chamber pressure can be about 1 mTorr to about 300 mTorr, about 5 mTorr to about 100 mTorr, about 5 mTorr to about 20 mTorr, e.g., about 10 mTorr. The plasma power can be relatively low when the ion energy is high. In some embodiments, the plasma power can be about 50 W to about 1000 W, about 100 W to about 500 W, or about 100 W to about 300 W, e.g., about 300 W. In some embodiments, the wafer bias is about 10 V to about 500 V, about 50 V to about 300 V, e.g., about 200 V. The plasma can be generated using a high RF frequency. In some embodiments, the RF frequency is 13.56 MHz. The duration of exposure to the inert gas plasma can be relatively short to avoid excessive exposure to UV radiation during plasma exposure. In some embodiments, the duration of exposure is about 0.5 seconds to about 5 seconds, about 1 second to about 3 seconds, e.g., about 2 seconds.

[0106] The inert gas plasma treatment for descumming and cleaning of unexposed resist residue has the additional benefit of hardening and solidifying the exposed resist, thereby enhancing its hard mask function in subsequent etching of the underlying substrate. This resist solidification is achieved by exposing the EUV-exposed resist to UV radiation generated by the inert gas plasma, which can continue even after the bias is turned off and descumming / smoothing is complete. If descumming / smoothing is not required or performed, an inert gas plasma cure may be performed instead.

[0107] Not only can the organic vapors of the present disclosure be used in dry development processes, but organic vapors such as trifluoroacetic acid can also be used in dry chamber cleaning or other processing operations for dry removal of metal-containing resists.

[0108] FIG. 5 shows a flow diagram of an exemplary method for dry chamber cleaning, according to some embodiments. The dry chamber cleaning may be performed after deposition, bevel and / or backside cleaning, baking, developing, or etching. In some embodiments, the dry chamber cleaning may be performed after deposition of the resist material in the same process chamber as deposition of the resist material. The operations of process 500 may be performed in a different order and / or with a different, fewer, or additional number of operations. Aspects of process 500 may be described with reference to FIGS. 6A-6D. One or more operations of process 200 may be performed using the apparatus described in any one of FIGS. 7-11B. In some embodiments, the operations of process 500 may be implemented, at least in part, according to software stored on one or more non-transitory computer-readable media.

[0109] At block 502 of process 500, a metal-containing resist material is deposited on a surface of a semiconductor substrate in a process chamber, with a portion of the metal-containing resist material forming a residue on one or more surfaces of the process chamber. The composition and deposition of such metal-containing resist materials can be described, for example, in International Patent Application No. PCT / US2019 / 31618, filed May 9, 2019, which is incorporated herein by reference for its disclosure of methods and materials applicable to the present disclosure. The method includes generating a polymerized organometallic material in the vapor phase and depositing it on a semiconductor substrate. In some embodiments, the metal-containing resist material is a metal oxide-containing EUV resist material. For example, elements in the metal-containing resist material are selected from the group consisting of tin, hafnium, tellurium, bismuth, indium, antimony, iodine, germanium, and combinations thereof. In some embodiments, the metal-containing resist material comprises an organometallic oxide, such as an organotin oxide.

[0110] In some embodiments, the process chamber in which the semiconductor substrate is disposed may be a dry deposition chamber. In other embodiments, the process chamber in which the semiconductor substrate is disposed may be a bevel edge and / or backside cleaning chamber, a PAB processing chamber, a PEB processing chamber, a development chamber, or an etch chamber. Any of the foregoing chambers may accumulate metal-containing resist material on their interior surfaces over time. As the number of semiconductor substrates processed in the processing chamber increases, the unintentional metal-containing resist material may build up on the interior surfaces as residue. Periodic cleaning is required to remove the unintentional deposits of metal-containing resist material. Cleaning can be performed "in situ," where dry chamber cleaning is performed in the same process chamber in which the unintentional metal-containing resist material is formed.

[0111] Residues can form on one or more surfaces of the process chamber, and the one or more surfaces may include one or more of the chamber walls, ceiling, floor, showerhead surface, nozzle surface, and substrate support surface. In some embodiments, the residues may form as a result of a dry deposition process, such as a CVD or ALD process. The thickness of the residue on one or more surfaces may increase over time as a result of additional processing (e.g., deposition) operations performed in the process chamber. In some embodiments, the average thickness of the residue is about 2 nm or more, about 3 nm or more, about 5 nm or more, or about 10 nm or more. Metal-containing resist materials tend to flake, shed particles, or peel from one or more surfaces, thereby contaminating subsequent semiconductor substrates during processing.

[0112] FIG. 6A shows a cross-sectional schematic view of a metal-containing EUV resist material 602 formed on a chamber wall 604 of a process chamber. The metal-containing EUV resist material 602 may include particles or clusters of metal oxide 606. The metal oxide 606 particles or clusters may be difficult to remove. In some embodiments, the metal-containing EUV resist material 602 is formed by a vapor deposition method such as CVD or ALD. Over time, the metal-containing EUV resist material 602 may thickly accumulate on the chamber wall 604 of the process chamber. The metal-containing EUV resist material 602 may be an organotin oxide. The metal oxide 606 particles or clusters may include tin oxide.

[0113] Returning to FIG. 5 , at block 504 of process 500, a dry etchant comprising an organic vapor is introduced into the process chamber, where the dry etchant at least partially removes residue on one or more surfaces of the process chamber. In some embodiments, the organic vapor is an organic acid. The organic acid may be a strong organic acid having a pKa of about 3.8 or less. In some embodiments, the organic acid comprises a carboxylic acid. In some embodiments, the organic acid comprises trifluoroacetic acid. The organic vapor may be halogenated or at least fluorinated. In some embodiments, the organic vapor comprises hexafluoroacetylacetone. In some embodiments, the organic vapor comprises mixed halide acetic acids such as trifluoroacetic anhydride, acetic anhydride, trichloroacetic acid, monofluoroacetic acid, difluoroacetic acid, chlorodifluoroacetic acid, sulfur-containing analogs of acetic acid, thioacetic acid, or thioglycolic acid. In some embodiments, the dry etchant comprises a mixture of a carboxylic acid and a hydrogen halide in the vapor phase. For example, the dry etchant comprises a mixture of acetic acid or formic acid with hydrogen chloride or hydrogen bromide. In some embodiments, the organic vapor may be flowed with or without an inert / carrier gas such as helium, neon, argon, xenon, and nitrogen.

[0114] In some embodiments, at least partial removal of the residue comprises reacting an organic vapor with the metal-containing resist material to form a volatile compound at a temperature less than about 200° C. In some embodiments, at least partial removal comprises substantial removal of the residue, where “substantial removal” refers to sufficient removal of the residue such that at least a portion of one or more surfaces is exposed after removal.

[0115] In some embodiments, the process chamber can be prepared at the desired conditions for dry chamber cleaning before introducing the dry etchant. Preparing the process chamber can achieve specific pressure conditions, levels of loose particles or film impurities, moisture levels, temperature conditions, or protection of surfaces or components (e.g., substrate support) within the process chamber from the dry etchant. In some embodiments, preparing the process chamber can include purging and / or pumping the process chamber to remove unwanted particles. To facilitate removal of unwanted particles within the process chamber, a purge gas can be flowed through the process chamber. Purging the organometallic precursor can be useful to avoid unwanted byproducts and ensure sufficient removal of the organometallic precursor before the dry chamber clean.

[0116] In some embodiments, the chamber walls and other components can be heated to release unreacted precursors. Heat can additionally or alternatively facilitate the removal of moisture within the process chamber. Without being limited by any theory, the presence of moisture may slow the reaction between the dry etchant and the metal-containing resist material used to remove the metal-containing resist material. Additionally, increasing the temperature within the process chamber increases the etch rate for removing the metal-containing resist material. One or more heaters within the process chamber can heat one or more surfaces to an elevated temperature. In some embodiments, the elevated temperature can be from about 20°C to about 180°C, from about 40°C to about 160°C, or from about 80°C to about 140°C.

[0117] In some implementations, preparing the process chamber can include providing a dummy substrate on a substrate support within the process chamber. Thus, the semiconductor substrate with the metal-containing resist material deposited thereon can be transferred out of the process chamber prior to the dry chamber clean. In this manner, the semiconductor substrate is not exposed to the dry etchant when removing residue of the metal-containing resist material from one or more surfaces of the process chamber. The dummy substrate can be provided on the substrate support to protect the substrate support (e.g., an electrostatic chuck) from exposure to the dry etchant during the dry chamber clean. Alternatively, protection of the substrate support can be achieved by providing a protective cover over the substrate support during the dry chamber clean.

[0118] The dry etchant may be introduced through a showerhead coupled to the process chamber or through a separate chamber inlet. The dry etchant may flow into the process chamber and react with the residue of the metal-containing resist material to form volatile products. Without being limited by any theory, the organometallic oxide resist material may have a tetrahedral coordination structure, and organic vapors such as trifluoroacetic acid may protonate the oxygen lone pairs to form volatile by-products. After the volatile by-products are formed, the process chamber may be pumped and purged to remove the volatile by-products. Additionally, the process chamber may be pumped and purged to remove residual dry etchant. Such residual dry etchant may cause undesired etching of the subsequent semiconductor substrate.

[0119] Dry chamber cleaning can be optimized for low etch selectivity or high etch rate of the resist material deposited in the process chamber. In this way, unwanted resist material can be removed quickly and efficiently. In some embodiments, higher temperatures and / or higher pressures can decrease the etch selectivity and increase the etch rate of the dry etchant. For example, resist material can be removed at an etch rate of up to 1 nm / sec. During exposure to the dry etchant, residues of the metal-containing resist material on one or more surfaces can be exposed to elevated temperatures. The elevated temperatures can be from about 20°C to about 180°C, from about 40°C to about 160°C, or from about 80°C to about 140°C. In some embodiments, residues of the metal-containing resist material react with organic vapors to form volatile compounds at temperatures below about 200°C. During exposure to the dry etchant, elevated pressures can be present in the process chamber. In some embodiments, the chamber pressure is from about 0.01 Torr to 765 Torr, from about 0.1 Torr to 100 Torr, or from about 0.1 Torr to about 6 Torr. In some embodiments, the chamber pressure is cycled between high and low pressures during exposure to the dry etchant. The flow rate of the organic vapor can be adjusted to control etch selectivity. In some embodiments, the flow rate of the organic vapor is about 0.05 SLM to about 10 SLM, or about 0.1 SLM to about 5 SLM.

[0120] As described above with respect to dry development, dry chamber cleaning is performed using organic vapors, such as organic acids, instead of halogen vapors. Halogen vapors, such as hydrogen halide vapors, tend to leave residual etching byproducts after removal of metal-containing resist materials. However, organic vapors, such as trifluoroacetic acid, form more volatile etching byproducts that are less difficult to remove from the process chamber. Organic vapors, such as trifluoroacetic acid, can be used for dry chamber cleaning in plasma-free thermal processes. In other words, residues of metal-containing resist materials are removed without applying a plasma. Residual carbon, contaminants, or other remaining materials may or may not be removed by exposure to a plasma. In some embodiments, following the introduction of the dry etchant, one or more surfaces may be exposed to an oxidizing gas, such as oxygen (O), ozone (O), carbon dioxide (CO), or carbon monoxide (CO).

[0121] Because it does not require the use of plasma and can clean as-deposited films (unexposed or uncrosslinked), the techniques described herein can also clean downstream and upstream components of the tool beyond the process chamber (e.g., exhaust lines from the process chamber to the vacuum pump).More generally, this dry cleaning method can be used to clean other contaminated parts and components with similar compositions of metals that have volatile by-products from organic vapors.

[0122] In some embodiments, the interior surface of the process chamber is compatible with the organic vapors of the present disclosure. Rather than the interior surface of the process chamber being resistant to plasma and resistant to vapors of halogens, such as hydrogen halides, the interior surface may comprise any material that is simply resistant to the organic vapors of the present disclosure. In some embodiments, the chamber walls of the process chamber may comprise aluminum oxide, anodized aluminum, or plastic.

[0123] In some embodiments, the process chamber may include a chamber component temperature controller coupled to one or more surfaces (e.g., chamber walls) to control the temperature. In some embodiments, the process chamber may include a gas inlet other than the showerhead for delivering a dry etchant. The gas inlet can be positioned in an area of ​​the process chamber where the concentration of metal-containing resist material is higher. The gas inlet can be positioned in an area of ​​the process chamber where the dry etchant is unlikely to reach by being delivered through the showerhead. In some embodiments, the gas inlet may be positioned below the substrate support, in a wall of the process chamber, and / or near the exhaust port of the process chamber. Multiple gas inlets can also be used to deliver the dry etchant to the process chamber, ensuring dry cleaning of the entire process chamber. In various embodiments, the dry etchant can be delivered to the process chamber through one or more gas inlets separate from the showerhead, and deposition gases can be delivered to the process chamber through the showerhead. In some embodiments, the showerhead can deliver separate gases by keeping the gases largely isolated within the showerhead. The showerhead can include multiple plenum volumes. The use of multiple exhaust lines can ensure separation of gases downstream of the process chamber. Switches can be operably coupled to the multiple exhaust lines to allow separation of dry etchant chemistries from deposition gases / precursors.

[0124] To protect the showerhead, a pressure differential can be used to prevent the dry etchant from entering (e.g., backflowing into) the showerhead. In some embodiments, the dry etchant can clean the interior surface of the showerhead by flowing the dry etchant through the showerhead. However, residual organic vapor or moisture may be retained within the channels of the showerhead. In some embodiments, the showerhead can be made of a transparent material and heated with an appropriate light source. For example, an irradiation source tuned to an appropriate wavelength (e.g., IR or blue wavelength) can directly heat and remove the residual organic vapor and / or moisture. Alternatively, the residual organic vapor and / or moisture can be removed by gas purging.

[0125] FIG. 6B shows a cross-sectional schematic view of the chamber walls 604 after a dry etchant has removed the metal-containing EUV resist material 602 from the chamber walls 604. The dry etchant may include an organic vapor, such as an organic acid, which may include trifluoroacetic acid. The chamber walls 604 may be heated to an elevated temperature to promote low etch selectivity. The process chamber may be at an elevated pressure to promote low etch selectivity. Removal of the metal-containing EUV resist material 602 may be performed without the use of a plasma. Residual particles or clusters of metal oxide 606 may remain on the chamber walls 604 after exposure to the dry etchant. Additionally, residual dry etchant 608 may remain within the process chamber.

[0126] Returning to FIG. 5 , in block 506 of process 500, the process chamber is optionally purged to remove residual dry etchant from the process chamber. The purging operation can include flowing a purge gas into the process chamber or a combination of flowing a purge gas and pumping the process chamber to a desired chamber pressure. The purge gas can be an inert gas and / or a reactive gas. The reactive gas can react with the residual dry etchant and facilitate its removal. The reactive gas can be, for example, a tin-based precursor, such as an organotin precursor. The inert gas can be argon, helium, xenon, or nitrogen. The chamber pressure can be from about 0.1 Torr to about 6 Torr.

[0127] In some embodiments, the purging operation can proceed at an elevated temperature. The elevated temperature can facilitate removal of organic vapors from the process chamber. In one example, one or more heaters coupled to one or more surfaces of the process chamber can heat the process chamber to an elevated temperature. In another example, one or more IR sources or LEDs can be installed within the process chamber to heat the process chamber to an elevated temperature. The elevated temperature can be from about 20°C to about 180°C, or from about 80°C to about 140°C.

[0128] In some embodiments, direct or remote plasma-based treatments are useful for facilitating the removal of residual dry etchant, which may coat the interior surfaces of the process chamber after dry chamber cleaning. In other embodiments, non-plasma treatments may be useful for accelerating the removal of residual dry etchant. The introduction of an oxidizing gas may oxidize the residual dry etchant. Thus, non-plasma treatments may include delivering a flow of ozone and / or oxygen gas.

[0129] 6C shows a cross-sectional schematic view of the chamber walls 604 after removing the residual dry etchant 608 from the process chamber. A pumping / purging operation can be performed to evacuate the residual dry etchant 608 from the process chamber. In some embodiments, the chamber walls 604 or other components of the process chamber can be heated to facilitate the release of the residual dry etchant 608. In some embodiments, a direct or remote plasma-based process can be applied to remove the residual dry etchant 608, and such a plasma-based process can include a fluorine-based plasma process, an oxygen-based plasma process, or a combination thereof. In some other embodiments, a non-plasma process can be applied to remove the residual dry etchant 608. Particles or clusters of metal oxide 606 may remain on the chamber walls 604.

[0130] Returning to FIG. 5 , in block 508 of process 500, one or more surfaces of the process chamber are optionally conditioned by forming a protective coating of a metal-containing resist material on the one or more surfaces of the process chamber. The average thickness of the protective coating can be less than the average thickness of the residue of the metal-containing resist material. In some implementations, the average thickness of the protective coating is about 1 nm or more, about 2 nm or more, about 3 nm or more, or about 1 nm to about 5 nm. Alternatively, the one or more surfaces are optionally conditioned by forming a protective coating made of a material different from the metal-containing resist material. Such a protective coating can be a variation of an organotin oxide. After exposure to the dry etchant, the one or more surfaces remain exposed. Exposed surfaces in the process chamber can be particularly vulnerable to attack by halogen-based species. The conditioning operation can protect the one or more surfaces. Additionally, the conditioning operation can cover any residual particles or metal oxide clusters adhering to the one or more surfaces. In this way, the metal oxide particles or clusters are less likely to contaminate the wafer during subsequent processing.

[0131] Conditioning of one or more surfaces of the process chamber can be performed by a vapor-based deposition technique, such as a CVD or ALD technique. Metalorganic materials are obtained in the vapor phase and deposited on one or more surfaces of the process chamber. Metalorganic materials can be deposited, for example, based on the vapor-phase reaction of an organotin precursor, such as isopropyl(tris)(dimethylamino)tin, with water vapor. The flow of water vapor can be relatively low. During conditioning, the substrate support can be protected or covered by a dummy wafer or other protective cover. Protective coatings can be formed on the chamber walls, floor, ceiling, or chamber components such as gas inlets, showerheads, and exhaust lines. Deposition of a protective coating of a metal-containing resist material can be followed by a pumping / purging operation to remove excess precursors and / or back-reactants. Conditioning one or more surfaces of the process chamber can trap residual metal oxide particles and limit particle contamination.

[0132] FIG. 6D shows a cross-sectional schematic view of a metal-containing EUV resist material 610 formed on a chamber wall 604 of a process chamber. The metal-containing EUV resist material 610 is redeposited in a conditioning operation to protect the chamber wall 604 during processing and to trap metal oxide 606 particles or clusters from wafer contamination. This is sometimes referred to as chamber seasoning. The metal-containing EUV resist material 610 is formed by a vapor deposition method such as CVD or ALD. In some embodiments, the metal-containing EUV resist material 610 may be an organotin oxide. Conditioning / seasoning the chamber wall 604 and other internal surfaces of the process chamber reduces the effects of undesired first wafer deposition when resuming deposition operations on a semiconductor substrate.

[0133] Although this disclosure frequently refers to the removal of exposed and / or developed EUV-sensitive films, the removal processes described do not necessarily involve the removal of EUV-sensitive films of similar composition (e.g., other MO x R yThis method can be extended to other films containing metal oxides where metals can form volatile by-products with organic vapors, including non-exposed EUV resist films, such as EUV-based films. In some embodiments, films other than EUV resists, such as hard masks, UV resists, or films of similar composition having other uses, can be removed by this method, and in this regard, the removal process described relates to the chemical composition of the film, rather than its function.

[0134] Device The apparatus of the present disclosure is configured for dry removal of EUV resist. The apparatus may be configured to perform dry development or dry chamber clean. The apparatus may be configured for other processing operations such as deposition, bevel and backside cleaning, post-apply bake, EUV scanning, post-exposure bake, photoresist rework, descum, smoothing, curing, and other operations. In some embodiments, the apparatus is configured to perform all drying operations. In some embodiments, the apparatus is configured to perform a combination of wet and dry operations. The apparatus may include a single wafer chamber or multiple stations within the same process chamber. When there are multiple stations within the same process chamber, various processing operations as described in this disclosure may be performed in different stations within the same process chamber. In one example, a PEB thermal treatment may be performed in one station and development may be performed in another station.

[0135] An apparatus configured for dry removal of EUV resist includes a process chamber having a substrate support. The apparatus can include a dry etching line coupled to the process chamber for delivering an etching gas. In some embodiments, the etching gas includes an organic vapor, such as trifluoroacetic acid. The apparatus can include one or more heaters for temperature control. Such heaters can be provided in the process chamber and / or the substrate support. In some embodiments, multiple gas inlets can be positioned within the process chamber to flow the etching gas near areas prone to unintended EUV resist formation. The apparatus can further include one or more sensors for sensing particle count, wafer count, thickness count, or other parameters for triggering a dry chamber clean and / or for triggering an endpoint of the dry chamber clean.

[0136] In some embodiments, the process chamber is made of an inexpensive material such as plastic, hi other embodiments, the process chamber is made of a metal such as anodized aluminum, or a ceramic such as aluminum oxide.

[0137] FIG. 7 illustrates a schematic diagram of an exemplary process station suitable for performing dry develop, clean, rework, descum, and smoothing operations, according to some embodiments. Multiple process stations 700 may be included in a common low-pressure process tool environment. For example, FIG. 8 illustrates one embodiment of a multi-station processing tool 800, such as a VECTOR® processing tool available from Lam Research, Inc. of Fremont, California. In some embodiments, one or more hardware parameters of the process tool 800 (including those described in detail below) may be programmatically adjusted by one or more computer controllers 850.

[0138] The process stations can be configured as modules within a cluster tool. Figure 10 illustrates a semiconductor process cluster tool architecture having a vacuum-integrated deposition and patterning module suitable for practicing embodiments described herein. Such a cluster process tool architecture can include resist deposition, resist exposure (EUV scanner), resist development, and etch modules, as described above and further below with reference to Figures 9 and 10.

[0139] In some embodiments, certain processing functions can be performed sequentially in the same module, such as dry development and etching or dry deposition and dry chamber cleaning. Embodiments of the present disclosure are also directed to methods and apparatus for receiving a wafer including an EUV resist thin film layer disposed on a layer or layer stack to be etched into a dry development / etch chamber following photopatterning in an EUV scanner, dry developing the photopatterned EUV resist thin film layer, and then etching the underlying layer using the patterned EUV resist as a mask, as described herein.

[0140] 7, the process station 700 is in fluid communication with a reactant delivery system 701 for delivering process gases to a distribution showerhead 706. The reactant delivery system 701 includes a mixing vessel 704 for blending and / or adjusting the process gases delivered to the showerhead 706. One or more mixing vessel inlet valves 720 can control the introduction of process gases into the mixing vessel 704. If plasma exposure is used, the plasma can also be delivered to the showerhead 706 or can be generated in the process station 700. As noted above, in at least some embodiments, non-plasma thermal exposure is preferred.

[0141] 7 includes an optional vaporization point 703 for vaporizing the liquid reactant supplied to the mixing vessel 704. In some embodiments, a liquid flow controller (LFC) can be provided upstream of the vaporization point 703 to control the mass flow rate of the liquid being vaporized and delivered to the process station 700. For example, the LFC can include a thermal mass flow meter (MFM) located downstream of the LFC. The plunger valve of the LFC can then be adjusted in response to a feedback control signal provided by a proportional-integral-derivative (PID) controller in electrical communication with the MFM.

[0142] The showerhead 706 distributes process gases toward the substrate 712. In the embodiment shown in Figure 7, the substrate 712 is shown positioned below the showerhead 706 and resting on a pedestal 708. The showerhead 706 may have any suitable shape and may have any suitable number and arrangement of ports for distributing process gases to the substrate 712.

[0143] In some embodiments, the pedestal 708 can be raised or lowered to expose the substrate 712 to the volume 707 between the substrate 712 and the showerhead 706. It will be appreciated that in some embodiments, the height of the pedestal can be programmatically adjusted by a suitable computer controller 750. In some embodiments, the showerhead 706 can have multiple plenum volumes with multiple temperature controls.

[0144] In some embodiments, the pedestal 708 may be temperature controlled via a heater 710. In some embodiments, the pedestal 708 may be heated to a temperature of greater than 0° C. to 300° C. or greater, such as 40° C. to 160° C., for example, about 80° C. to 140° C., during non-plasma thermal exposure of the photopatterned resist to an organic vapor developing chemistry, such as trifluoroacetic acid, as described in disclosed embodiments. In some embodiments, the heater 710 of the pedestal 708 may include multiple independently controllable temperature control zones.

[0145] Additionally, in some embodiments, pressure control for the process station 700 may be provided by a butterfly valve 718. As shown in the embodiment of Figure 7, the butterfly valve 718 throttles the vacuum provided by a downstream vacuum pump (not shown). However, in some embodiments, pressure control for the process station 700 may also be adjusted by varying the flow rate of one or more gases introduced to the process station 700.

[0146] In some implementations, the position of the showerhead 706 can be adjusted relative to the pedestal 708 to vary the volume 707 between the substrate 712 and the showerhead 706. Furthermore, it will be understood that the vertical position of the pedestal 708 and / or the showerhead 706 may be varied by any suitable mechanism within the scope of the present disclosure. In some implementations, the pedestal 708 may include a rotation axis for rotating the orientation of the substrate 712. It will be understood that in some implementations, one or more of these exemplary adjustments may be implemented programmatically by one or more suitable computer controllers.

[0147] When a plasma may be used, for example, in a descum or smoothing operation, the showerhead 706 and pedestal 708 are in electrical communication with a radio frequency (RF) power supply 714 and matching network 716 to power the plasma. In some implementations, the plasma energy can be controlled by controlling one or more of the process station pressure, gas concentration, RF source power, RF source frequency, and plasma power pulse timing. For example, the RF power supply 714 and matching network 716 can be operated at any suitable power to form a plasma having a desired composition of radical species. An example of a suitable power is up to about 500 W.

[0148] In some embodiments, instructions for the controller 750 may be provided via input / output control (IOC) sequence instructions. In one example, instructions for setting conditions for a process step may be included in a corresponding recipe step of a process recipe. In some cases, process recipe steps may be arranged in a sequence such that all instructions for a process step are executed simultaneously with that process step. In some embodiments, instructions for setting one or more reactor parameters may be included in a recipe step. For example, a recipe step may include instructions for setting a flow rate of a dry development chemical reactant gas, such as trifluoroacetic acid, and a time delay instruction for the recipe step. In some embodiments, the controller 750 may include any of the features described below with respect to the system controller 850 of FIG. 8.

[0149] As described above, one or more process stations can be included in a multi-station processing tool. FIG. 8 shows a schematic diagram of one embodiment of a multi-station processing tool 800 including an inbound load lock 802 and an outbound load lock 804, either or both of which may include a remote plasma source. A robot 806 is configured to move wafers at atmospheric pressure from a cassette loaded via a pod 808 to the inbound load lock 802 through an atmospheric pressure port 810. The wafer is placed by the robot 806 on a pedestal 812 of the inbound load lock 802, the atmospheric pressure port 810 is closed, and the load lock is pumped down. If the inbound load lock 802 includes a remote plasma source, the wafer may undergo remote plasma processing to treat the substrate surface within the load lock before being introduced into the processing chamber 814. Additionally, the wafer may also be heated in the inbound load lock 802, for example, to remove moisture and absorbed gases. Next, a chamber transfer port 816 to the processing chamber 814 is opened, and another robot (not shown) places the wafer into the reactor on a pedestal in the first station shown in the reactor for processing. While the embodiment shown in Figure 8 includes a load lock, it will be understood that in some embodiments, the wafer may enter the process station directly.

[0150] The illustrated processing chamber 814 includes four process stations, numbered 1 through 4 in the embodiment shown in FIG. 8 . Each station has a heated pedestal (shown at 818 for station 1) and a gas line inlet. It will be understood that in some embodiments, each process station may have a different purpose or multiple purposes. For example, in some embodiments, a process station may be switchable between a dry development mode and an etch process mode. Additionally or alternatively, in some embodiments, the processing chamber 814 may include one or more corresponding pairs of dry development and etch process stations. While the illustrated processing chamber 814 includes four stations, it will be understood that a processing chamber according to the present disclosure may have any suitable number of stations. For example, in some embodiments, the processing chamber may have five or more stations, while in other embodiments, the processing chamber may have three or fewer stations.

[0151] FIG. 8 illustrates one embodiment of a wafer handling system 890 for transferring wafers within the processing chamber 814. In some embodiments, the wafer handling system 890 can transfer wafers between various process stations and / or between process stations and load locks. It will be understood that any suitable wafer handling system may be used. Non-limiting examples include a wafer carousel and a wafer handling robot. FIG. 8 also illustrates one embodiment of a system controller 850 used to control the process conditions and hardware states of the process tool 800. The system controller 850 can include one or more memory devices 856, one or more mass storage devices 854, and one or more processors 852. The processor 852 can include a CPU or computer, analog and / or digital input / output connections, stepper motor controller boards, etc.

[0152] In some embodiments, system controller 850 controls all of the activity of process tool 800. System controller 850 executes system control software 858 stored on mass storage device 854, loaded into memory device 856, and executed on processor 852. Alternatively, control logic may be hard-coded into controller 850. Application-specific integrated circuits, programmable logic devices (e.g., field-programmable gate arrays, or FPGAs), or the like may be used for these purposes. In the following description, wherever "software" or "code" is used, functionally equivalent hard-coded logic may be used instead. System control software 858 may include instructions for controlling the timing, mixture of gases, gas flow rates, chamber and / or station pressure, chamber and / or station temperature, wafer temperature, target power levels, RF power levels, substrate pedestal, chuck and / or susceptor position, and other parameters of a particular process performed by process tool 800. System control software 858 may be configured in any suitable manner. For example, various process tool component subroutines or control objects may be written to control the operation of the process tool components used to perform the various process tool processes. The system control software 858 may be coded in any suitable computer-readable programming language.

[0153] In some embodiments, the system control software 858 may include input / output control (IOC) sequencing instructions for controlling the various parameters described above. In some embodiments, other computer software and / or programs stored on the mass storage device 854 and / or memory device 856 associated with the system controller 850 may also be used. Examples of programs or sections of programs for this purpose include a substrate positioning program, a process gas control program, a pressure control program, a heater control program, and a plasma control program.

[0154] The substrate positioning program may include program code for process tool components used to load the substrate onto the pedestal 818 and control the spacing between the substrate and other parts of the process tool 800 .

[0155] The process gas control program can include code for controlling organic vapor composition (e.g., trifluoroacetic acid as described herein) and flow rates to stabilize the pressure of the process station, and optionally, code for flowing gases to one or more process stations prior to deposition. The pressure control program can include code for controlling the pressure of the process station by, for example, adjusting a throttle valve in the exhaust system of the process station, gas flow to the process station, etc.

[0156] The heater control program may include code for controlling the current to a heating unit used to heat the substrate, or the heater control program may control the delivery of a heat transfer gas (such as helium) to the substrate.

[0157] The plasma control program may include code for setting RF power levels applied to process electrodes in one or more process stations in accordance with embodiments herein.

[0158] The pressure control program can include code for maintaining pressure within the reaction chamber according to embodiments herein.

[0159] In some embodiments, there may be a user interface associated with the system controller 850. The user interface may include a display screen, a graphical software display of equipment and / or process conditions, and user input devices such as a pointing device, keyboard, touch screen, microphone, etc.

[0160] In some implementations, the parameters adjusted by the system controller 850 may relate to process conditions. Non-limiting examples include process gas composition and flow rates, temperature, pressure, plasma conditions (such as RF bias power levels), etc. These parameters may be provided to the user in the form of a recipe or may be entered using a user interface.

[0161] Signals for monitoring the process may be provided by analog and / or digital input connections of the system controller 850 from various process tool sensors. Signals for controlling the process can be output at analog and digital output connections of the process tool 800. Non-limiting examples of process tool sensors that may be monitored include mass flow controllers, pressure sensors (such as pressure gauges), thermocouples, etc. Appropriately programmed feedback and control algorithms can be used with data from these sensors to maintain process conditions.

[0162] The system controller 850 can provide program instructions for carrying out the deposition processes described above. The program instructions can control various process parameters such as DC power levels, RF bias power levels, pressure, temperature, etc. The instructions can control parameters for operating development, cleaning, and / or etching processes according to various embodiments described herein.

[0163] System controller 850 typically includes one or more memory devices and one or more processors configured to execute instructions such that the apparatus performs methods according to the disclosed embodiments. Machine-readable media containing instructions for controlling process operations according to the disclosed embodiments may be coupled to system controller 850.

[0164] In some embodiments, the system controller 850 is part of a system, such as may be part of the examples described above. Such systems may include semiconductor processing equipment, including one or more processing tools, one or more chambers, one or more processing platforms, and / or specific processing components (e.g., wafer pedestals, gas flow systems, etc.). These systems may be integrated with electronics for controlling system operation before, during, and after semiconductor wafer or substrate processing. Such electronics may be referred to as a "controller" and may control various components or subcomponents of one or more systems. The system controller 850 may be programmed to control any of the processes disclosed herein, depending on the processing conditions and / or type of system. Such processes may include process gas delivery, 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, position and motion settings, wafer transfer to and from tools and other transfer tools connected or interfaced with a particular system, and / or wafer transfer to and from load locks.

[0165] Broadly, system controller 850 may be defined as electronic equipment having various integrated circuits, logic, memory, and / or software that receive instructions, issue instructions, control operations, enable cleaning operations, enable endpoint measurements, etc. 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, i.e., microcontrollers, that execute program instructions (e.g., software). Program instructions may be instructions communicated to system controller 850 in the form of various individual settings (or program files) that define operational parameters for performing a particular process on or for a semiconductor wafer or for a system. The operational parameters, in some embodiments, may be part of a recipe defined by a process engineer to implement one or more processing steps in the fabrication of one or more layers, materials, metals, oxides, silicon, silicon dioxide, surfaces, circuits, and / or wafer dies.

[0166] In some embodiments, the system controller 850 may be part of, coupled to, or a combination of a computer integrated with, coupled to, or otherwise networked to the system. For example, the system controller 850 may be in the “cloud” or all or part of a fab host computer system. This allows for remote access to wafer processing. The computer may provide remote access to the system to monitor the current progress of a fabrication operation, review the history of past fabrication operations, review trends or performance criteria from multiple fabrication operations, modify parameters of a current process, set processing steps following a current process, or initiate a new process. In some examples, a remote computer (e.g., a server) can provide process recipes to the system over a network. Such a network may include a local network or the Internet. The remote computer may include a user interface that allows entry or programming of parameters and / or settings, which are then communicated to the system from the remote computer. In some examples, the system controller 850 receives instructions in the form of data. Such data may identify parameters for each processing step performed during one or more operations. It should be understood that the parameters may be specific to the type of process being performed and the type of tool that system controller 850 is configured to interface with or control. Thus, as described above, system controller 850 may be distributed, for example, by including one or more individual controllers that are networked together and cooperate toward a common purpose (such as the processes and controls described herein).An example of a distributed controller for such purposes would include one or more integrated circuits on the chamber that communicate with one or more integrated circuits located remotely (e.g., at the platform level or as part of a remote computer) and coupled to control the process in the chamber.

[0167] Exemplary systems may include, but are not limited to, a plasma etch chamber or module, a deposition chamber or module, a spin rinse chamber or module, a metal plating chamber or module, a cleaning 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 ALD chamber or module, an atomic layer etch (ALE) chamber or module, an ion implantation chamber or module, a tracker chamber or module, an EUV lithography chamber (scanner) or module, a development chamber or module, and any other semiconductor processing system that may be associated with or used in the fabrication and / or manufacturing of semiconductor wafers.

[0168] As described above, depending on the process step or steps being performed by the tool, system controller 850 may communicate with one or more other tool circuits or modules, other tool components, cluster tools, other tool interfaces, adjacent tools, nearby tools, tools located throughout the factory, a main computer, another controller, or tools used in material transport to and from tool locations and / or load ports in a semiconductor fabrication factory.

[0169] In certain embodiments, an ICP reactor is described herein that may be suitable for etching operations suitable for practicing some embodiments. Although an ICP reactor is described herein, it should be understood that in some embodiments, a capacitively coupled plasma reactor may also be used.

[0170] 9 shows a schematic cross-sectional view of an inductively coupled plasma apparatus 900 suitable for performing certain embodiments or aspects of embodiments, such as dry developing, cleaning, and / or etching, an example of which is the Kiyo® reactor manufactured by Lam Research, Inc. of Fremont, Calif. In other embodiments, other tools or tool types capable of performing the dry developing, cleaning, and / or etching processes described herein may be used.

[0171] The inductively coupled plasma apparatus 900 includes an overall process chamber 924 structurally defined by a chamber wall 901 and a window 911. The chamber wall 901 can be fabricated from stainless steel, aluminum, or plastic. The window 911 can be fabricated from quartz or other dielectric materials. An optional internal plasma grid 950 divides the overall process chamber into an upper subchamber 902 and a lower subchamber 903. In many embodiments, the plasma grid 950 can be removed, thereby utilizing the chamber space consisting of the subchambers 902 and 903. A chuck 917 is positioned within the lower subchamber 903 near the bottom inner surface. The chuck 917 is configured to receive and hold a semiconductor wafer 919 on which etching and deposition processes are performed. If present, the chuck 917 can be an electrostatic chuck for supporting the wafer 919. In some embodiments, an edge ring (not shown) surrounds the chuck 917 and, if present on the chuck 917, has an upper surface that is approximately planar with the upper surface of the wafer 919. The chuck 917 also includes an electrostatic electrode for chucking and dechucking the wafer 919. A filter and DC clamp power supply (not shown) may be provided for this purpose. Other control systems for lifting the wafer 919 from the chuck 917 may also be provided. The chuck 917 may be charged using an RF power supply 923. The RF power supply 923 is connected to a matching network 921 through connection 927. The matching network 921 is connected to the chuck 917 through connection 925. In this manner, the RF power supply 923 is connected to the chuck 917. In various embodiments, the bias power of the electrostatic chuck may be set to approximately 50 V or may be set to a different bias power depending on the process being performed according to the disclosed embodiments. For example, the bias power may be between approximately 20 V and approximately 100 V, or between approximately 30 V and approximately 150 V.

[0172] Elements for plasma generation include a coil 933, positioned over the window 911. In some embodiments, a coil is not used in the disclosed embodiments. The coil 933 is fabricated from a conductive material and includes at least one full turn. The example coil 933 shown in FIG. 9 includes three turns. A cross section of the coil 933 is indicated by symbols, with the coil having an "X" extending into the page and the coil having a "●" extending out of the page. Elements for plasma generation also include an RF power supply 941 configured to provide RF power to the coil 933. Generally, the RF power supply 941 is connected to a matching circuit 939 through connection 945. The matching circuit 939 is connected to the coil 933 through connection 943. In this manner, the RF power supply 941 is connected to the coil 933. An optional Faraday shield 949 is positioned between the coil 933 and the window 911. The Faraday shield 949 may be maintained in a spaced apart relationship relative to the coil 933. In some embodiments, the Faraday shield 949 is positioned directly above the window 911. In some embodiments, the Faraday shield 949 is between the window 911 and the chuck 917. In some embodiments, the Faraday shield 949 is not maintained in a spaced apart relationship with respect to the coil 933. For example, the Faraday shield 949 may be directly below the window 911 with no gap. The coil 933, the Faraday shield 949, and the window 911 are each configured to be substantially parallel to one another. The Faraday shield 949 can prevent metals or other species from depositing on the window 911 of the process chamber 924.

[0173] Process gases can enter the process chamber through one or more main gas inlets 960 and / or one or more side gas inlets 970 positioned in the upper subchamber 902. Similarly, although not explicitly shown, similar gas inlets can be used to supply process gases to the capacitively coupled plasma processing chamber. A vacuum pump, e.g., a single-stage or two-stage mechanical dry pump and / or turbomolecular pump 940, can be used to draw process gases from the process chamber 924 and maintain pressure within the process chamber 924. For example, the vacuum pump can be used to evacuate the lower subchamber 903 during a purge operation. A valve-controlled conduit can be used to fluidly connect the vacuum pump to the process chamber 924 to selectively control the application of the vacuum environment provided by the vacuum pump. This can be done using a closed-loop controlled flow restriction device, such as a throttle valve (not shown) or a pendulum valve (not shown), during plasma processing operations. Similarly, a vacuum pump and valve-controlled fluid connection to the capacitively coupled plasma processing chamber can also be used.

[0174] During operation of the apparatus 900, one or more process gases can be supplied through the gas inlets 960 and / or 970. In certain embodiments, process gases can be supplied only through the main gas inlet 960 or only through the side gas inlet 970. In some cases, the gas inlets shown in the figure can be replaced with more complex gas inlets, such as one or more showerheads. The Faraday shield 949 and / or optional grid 950 can include internal channels and holes that allow delivery of process gases to the process chamber 924. Either or both the Faraday shield 949 and optional grid 950 can function as showerheads for delivering process gases. In some embodiments, a liquid vaporization and delivery system can be positioned upstream of the process chamber 924, whereby liquid reactants or precursors are vaporized and the vaporized reactants or precursors are introduced into the process chamber 924 via the gas inlets 960 and / or 970.

[0175] Radio frequency power is supplied from RF power supply 941 to coil 933, causing RF current to flow through coil 933. The RF current flowing through coil 933 generates an electromagnetic field around coil 933. The electromagnetic field generates an induced current within upper subchamber 902. Physical and chemical interactions of the various generated ions and radicals with wafer 919 etch features in wafer 919 and selectively deposit layers on wafer 919.

[0176] When a plasma grid 950 is used such that both an upper subchamber 902 and a lower subchamber 903 are present, induced currents act on the gas present in the upper subchamber 902, generating an electron-ion plasma in the upper subchamber 902. The optional internal plasma grid 950 limits the number of thermal electrons in the lower subchamber 903. In some embodiments, the apparatus 900 is designed and operated such that the plasma present in the lower subchamber 903 is an ion-ion plasma.

[0177] Both the upper electron-ion plasma and the lower ion-ion plasma can contain positive and negative ions, but the ion-ion plasma has a higher ratio of negative ions to positive ions. Volatile etching and / or deposition byproducts can be removed from the lower subchamber 903 through port 922. The chuck 917 disclosed herein can operate at high temperatures ranging from about 10°C to about 250°C. The temperature depends on the process operation and the specific recipe.

[0178] The apparatus 900 may be coupled to equipment (not shown) when installed in a clean room or fabrication facility. The equipment includes plumbing to provide process gases, vacuum, temperature control, and environmental particle control. These equipment are coupled to the apparatus 900 when installed in the target fabrication facility. Additionally, the apparatus 900 may be coupled to a transfer chamber that allows a robot to move semiconductor wafers in and out of the apparatus 900 using typical automated operations.

[0179] In some embodiments, a system controller 930 (which may include one or more physical or logical controllers) controls some or all of the operation of the process chamber 924. The system controller 930 may include one or more memory devices and one or more processors. In some embodiments, the apparatus 900 includes a switching system for controlling flow rates and durations when the disclosed embodiments are performed. In some embodiments, the apparatus 900 may have a switching time of up to about 500 ms, or up to about 750 ms. The switching time may depend on the flow chemistry, the selected recipe, the reactor architecture, and other factors.

[0180] In some implementations, the system controller 930 is part of a system, such as may be part of the examples described above. Such systems may include semiconductor processing equipment, including one or more processing tools, one or more chambers, one or more processing platforms, and / or specific processing components (e.g., wafer pedestals, gas flow systems, etc.). These systems may be integrated with electronics for controlling system operation before, during, and after semiconductor wafer or substrate processing. Such electronics may be integrated into the system controller 930 and control various components or subcomponents of one or more systems. The system controller 930 may be programmed to control any of the processes disclosed herein, depending on the processing parameters and / or type of system. Such processes may include process gas delivery, 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, position and motion settings, wafer transfer to and from tools and other transfer tools connected or interfaced with a particular system, and / or wafer transfer to and from load locks.

[0181] Broadly, the system controller 930 may be defined as electronic equipment having various integrated circuits, logic, memory, and / or software that receive instructions, issue instructions, control operations, enable cleaning operations, enable endpoint measurements, etc. 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, i.e., microcontrollers, that execute program instructions (e.g., software). The program instructions may be instructions communicated to the controller in the form of various individual settings (or program files) that define operational parameters for performing a particular process on or for a semiconductor wafer or for a system. The operational parameters, in some implementations, may be part of a recipe defined by a process engineer to accomplish one or more processing steps in the fabrication or removal of one or more layers, materials, metals, oxides, silicon, silicon dioxide, surfaces, circuits, and / or wafer die.

[0182] In some embodiments, the system controller 930 may be part of, coupled to, or a combination of a computer integrated with, coupled to, or otherwise networked to the system. For example, the controller may be in the “cloud” or all or part of a fab host computer system. This allows for remote access to wafer processing. The computer may provide remote access to the system to monitor the current progress of a fabrication operation, review the history of past fabrication operations, review trends or performance criteria from multiple fabrication operations, modify parameters of a current process, configure processing steps following a current process, or initiate a new process. In some examples, a remote computer (e.g., a server) can provide process recipes to the system over a network. Such a network may include a local network or the Internet. The remote computer may include a user interface that allows entry or programming of parameters and / or settings, which are then communicated to the system from the remote computer. In some examples, the system controller 930 receives instructions in the form of data. Such data may identify parameters for each processing step performed during one or more operations. It should be understood that the parameters may be specific to the type of process being performed and the type of tool the controller is configured to interface with or control. Thus, as described above, the system controller 930 may be distributed, for example, by including one or more individual controllers networked together and working together toward a common purpose (such as the processes and controls described herein).An example of a distributed controller for such purposes would include one or more integrated circuits on the chamber that communicate with one or more integrated circuits located remotely (e.g., at the platform level or as part of a remote computer) and coupled to control the process in the chamber.

[0183] Exemplary systems may include, but are not limited to, a plasma etch chamber or module, a deposition chamber or module, a spin rinse chamber or module, a metal plating chamber or module, a cleaning 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 ALD chamber or module, an ALE chamber or module, an ion implantation chamber or module, a tracker chamber or module, an EUV lithography chamber (scanner) or module, a dry develop chamber or module, and any other semiconductor processing system that may be associated with or used in the fabrication and / or manufacturing of semiconductor wafers.

[0184] As described above, depending on the process step or steps being performed by the tool, the controller may communicate with one or more other tool circuits or modules, other tool components, cluster tools, other tool interfaces, adjacent tools, nearby tools, tools located throughout the factory, a main computer, another controller, or tools used in material transport to and from tool locations and / or load ports in a semiconductor fabrication factory.

[0185] EUVL patterning can be performed using any suitable tool, often referred to as a scanner, such as the TWINSCAN NXE:3300B® platform supplied by ASML, Veldhoven, The Netherlands. The EUVL patterning tool may be a standalone device from which substrates are loaded and unloaded for the deposition and etching described herein. Alternatively, as described below, the EUVL patterning tool may be a module on a larger, multi-component tool. Figure 10 illustrates a semiconductor process cluster tool architecture having vacuum-integrated deposition, EUV patterning, and dry develop / etch modules interfaced with a vacuum transfer module, suitable for carrying out the processes described herein. While the processes can be performed without such vacuum-integrated equipment, such equipment may be advantageous in some embodiments.

[0186] 10 illustrates a semiconductor process cluster tool architecture having a vacuum-integrated deposition and patterning module interfaced with a vacuum transfer module suitable for carrying out the processes described herein. The arrangement of transfer modules for "transferring" wafers between multiple storage facilities and processing modules is sometimes referred to as a "cluster tool architecture" system. The deposition and patterning modules are vacuum-integrated according to the requirements of a particular process. Other modules, such as for etching, can also be included in the cluster.

[0187] A vacuum transfer module (VTM) 1038 interfaces with four processing modules 1020a-1020d, which can be individually optimized to perform various fabrication processes. By way of example, processing modules 1020a-1020d can be implemented to perform deposition, evaporation, ELD, dry develop, clean, etch, strip, and / or other semiconductor processes. For example, module 1020a can be an ALD reactor that can be operated to perform the non-plasma thermal atomic layer deposition described herein, such as a Vector tool available from Lam Research, Inc. of Fremont, California. And module 1020b can be a PECVD tool, such as a Lam Vector®. It should be understood that the figures are not necessarily drawn to scale.

[0188] Airlocks 1042 and 1046, also known as load locks or transfer modules, interface with VTM 1038 and patterning module 1040. For example, as noted above, a suitable patterning module could be a TWINSCAN NXE:3300B® platform supplied by ASML, Veldhoven, The Netherlands. This tool architecture allows workpieces, such as semiconductor substrates or wafers, to be transferred under vacuum to prevent reaction prior to exposure. Integration of the deposition module with the lithography tool is facilitated by the fact that EUVL also requires significantly reduced pressure, given the strong optical absorption of incident photons by ambient gases such as HO and O.

[0189] As noted above, this integrated architecture is just one possible implementation of a tool for performing the described process. The process can also be performed using more conventional standalone EUVL scanners and, modularly, using deposition reactors such as the Lam Vector tool described with reference to FIG. 10 but without an integrated patterning module, either standalone or integrated in a cluster architecture with other etch, strip, etc. tools (e.g., Lam Kiyo or Gamma tools).

[0190] Airlock 1042 may be an "outgoing" load lock, referring to the transfer of substrates from the VTM 1038 servicing deposition module 1020a to the patterning module 1040, and airlock 1046 may be an "incoming" load lock, referring to the transfer of substrates from the patterning module 1040 back to the VTM 1038. The incoming load lock 1046 may also provide an interface to the outside of the tool for substrate access and egress. Each process module has a facet that interfaces the module to the VTM 1038. For example, deposition process module 1020a has facet 1036. Within each facet, sensors, such as sensors 1-18 shown, are used to detect the passage of wafer 1026 as it moves between its respective stations. Patterning module 1040 and airlocks 1042 and 1046 may similarly include additional facets and sensors not shown.

[0191] The main VTM robot 1022 transfers wafers 1026 between modules, including airlocks 1042 and 1046. In one embodiment, the robot 1022 has one arm, and in another embodiment, the robot 1022 has two arms, each arm having an end effector 1024 that lifts wafers, such as wafer 1026, for transfer. A front-end robot 1044 is used therein to transfer wafers 1026 from the output airlock 1042 to the patterning module 1040 and from the patterning module 1040 to the input airlock 1046. The front-end robot 1044 can also transfer wafers 1026 between the input load lock and the exterior of the tool for substrate access and egress. Because the input airlock module 1046 has the ability to adapt environments between atmospheric pressure and vacuum, wafers 1026 can be moved between the two pressure environments without damage.

[0192] It should be noted that EUVL tools typically operate at a higher vacuum than deposition tools. In this case, it is desirable to increase the vacuum environment of the substrate during transfer between the deposition tool and the EUVL tool to allow for degassing of the substrate before entering the patterning tool. The unloading airlock 1042 can provide this function by holding the transferred wafer at a low pressure no higher than the pressure in the patterning module 1040 for a period of time and venting the off-gassing, thereby preventing contamination of the optics of the patterning module 1040 by off-gassing from the substrate. A suitable pressure for the exhaust off-gas airlock is 1E-8 Torr or less.

[0193] In some embodiments, a system controller 1050 (which may include one or more physical or logical controllers) controls some or all of the operation of the cluster tool and / or its separate modules. Note that the controller may be local to the cluster architecture, located outside the cluster architecture on the manufacturing floor, or located at a remote location and connected to the cluster architecture via a network. The system controller 1050 may include one or more memory devices and one or more processors. The processor may include a central processing unit (CPU) or computer, analog and / or digital input / output connections, stepper motor controller boards, and other similar components. Instructions for implementing appropriate control operations are executed on the processor. These instructions may be stored in a memory device associated with the controller or provided over a network. In certain embodiments, the system controller executes system control software.

[0194] The system control software may include instructions for controlling the timing of application and / or magnitude of any aspect of tool or module operation. The system control software may be configured in any suitable manner. For example, various process tool component subroutines or control objects may be written to control the operation of process tool components necessary to perform various process tool processes. The system control software may be coded in any suitable computer-readable programming language. In some embodiments, the system control software includes input / output control (IOC) sequencing instructions for controlling the various parameters described above. For example, each stage of a semiconductor fabrication process may include one or more instructions executed by the system controller. For example, instructions for setting process conditions for condensation, deposition, vapor deposition, patterning, and / or etching stages may be included in the corresponding recipe stage.

[0195] In various embodiments, an apparatus for forming a negative pattern mask is provided. The apparatus can include process chambers for patterning, deposition, and etching, and a controller including instructions for forming the negative pattern mask. The instructions can include code for, in the process chamber, patterning features in a chemically amplified (CAR) resist on a semiconductor substrate by EUV exposure to expose a surface of the substrate, developing the photopatterned resist, and etching an underlying layer or layer stack using the patterned resist as a mask. The development can be performed using an organic vapor, such as an organic acid.

[0196] It should be noted that the computer controlling the movement of the wafers may be local to the cluster architecture, may be located outside the cluster architecture on the manufacturing floor, or may be located at a remote location and connected to the cluster architecture via a network. The controller described above with respect to any of Figures 7, 8, or 9 may be implemented using the tool of Figure 10.

[0197] FIG. 11A shows an example of a deposition chamber for vapor-based deposition of a metal-containing resist material, according to some embodiments. As can be seen, an apparatus 1100 is shown having a process chamber 1102 including a lid 1108. The process chamber 1102 can include a wafer transfer passage 1104 through one of its walls, sized to allow a substrate 1122 to pass through and enter the interior of the process chamber 1102, where the substrate 1122 can be placed on a wafer support 1124. The wafer transfer passage 1104 can have a gate valve 1106 or similar door mechanism operable to seal or open the wafer transfer passage 1104, thereby isolating the environment within the process chamber 1102 from the environment on the other side of the gate valve 1106. For example, the process chamber 1102 can be provided with a substrate 1122 via a wafer handling robot located in an adjacent transfer chamber. Such a transfer chamber may, for example, have multiple process chambers 1102 arranged around its periphery, with each such process chamber 1102 connected to the transfer chamber via a corresponding gate valve 1106 .

[0198] The wafer support 1124 may include, for example, an electrostatic chuck (ESC) 1126 that may be used to provide a wafer support surface for supporting the substrate 1122. The ESC 1126 may include, for example, a base plate 1134 bonded to a top plate 1128 that rests on the base plate 1134. The top plate 1128 may be made of, for example, a ceramic material and may have several other components embedded therein. In the illustrated example, the top plate 1128 has two separate electrical systems embedded therein. One such system is an electrostatic clamping electrode system, which may have one or more clamping electrodes 1132 that may be used to generate an electric charge in the substrate 1122, causing the substrate 1122 to be attracted to the wafer support surface of the top plate 1128. In the embodiment of FIG. 11A , there are two clamping electrodes 1132 that provide a bipolar electrostatic clamping system, but in some embodiments, only a single clamping electrode 1132 may be used to provide a monopolar electrostatic clamping system.

[0199] Another system is a thermal control system that can be used to control the temperature of the substrate 1122 during processing conditions. In FIG. 11A , the thermal control system is a multi-zone thermal control system featuring four annular resistive heater traces 1130a, 1130b, 1130c, and 1130d that are concentric with one another and positioned beneath a clamping electrode 1132. The central resistive heater trace 1130a may, in some embodiments, fill a generally circular area, and each resistive heater trace 1130a / b / c / d may follow a generally serpentine or serpentine path within its corresponding annular area. Individual control of each resistive heater trace 1130a / b / c / d can provide various radial heating profiles to the top plate 1128, and such a four-zone heating system may be controlled to maintain the substrate 1122 with, for example, a temperature uniformity of ±0.5°C in some cases. Although the device 1100 of FIG. 11A features a four-zone heating system within the ESC 1126, in other embodiments, single-zone or multi-zone heating systems having more or less than four zones can be used.

[0200] For example, in some implementations of the temperature control mechanisms described above, a heat pump may be used in place of the resistive heating traces. For example, in some implementations, the resistive heater traces may be replaced or augmented by Peltier junctions or other similar devices that can be controlled to "pump" heat from one side to the other. Such a mechanism may be used, for example, to draw heat from the top plate 1128 (and thus the substrate 1122) and direct the heat to the base plate 1134 and heat exchange passages 1136, thereby allowing the substrate 1122 to cool more quickly and effectively, as desired.

[0201] The ESC 1126 may also include a base plate 1134, which may be used, for example, to provide structural support to the underside of the top plate 1128 and may also act as a heat distribution system. For example, the base plate 1134 may include one or more heat exchange passages 1136 arranged generally dispersed throughout the base plate 1134; for example, the heat exchange passages 1136 may follow a serpentine, circular switchback, or spiral pattern around the center of the base plate 1134. During use, a heat exchange medium, for example, water or an inert fluorinated liquid, may be circulated through the heat exchange passages 1136. The flow rate and temperature of the heat exchange medium may be externally controlled to produce specific heating or cooling behavior within the base plate 1134.

[0202] The ESC 1126 may be supported by, for example, a wafer support housing 1142 connected to and supported by wafer support columns 1144. The wafer support columns 1144 may have routing passages 1148 or other passages, for example, for routing cabling, fluid flow conduits, and other equipment to the underside of the base plate 1134 and / or top plate 1128. For example, although not shown in FIG. 11A , cabling for supplying power to the resistive heater traces 1130a / b / c / d may be routed through the routing passages 1148, as may cabling for supplying power to the clamp electrodes 1132. Other cables, for example, cables for temperature sensors, may also be routed through the routing passages 1148 to locations internal to the wafer support 1124. In embodiments having a temperature-controllable base plate 1134, conduits for transporting heat exchange media to and from the base plate 1134 may also be routed through the routing passages 1148. To avoid undue clutter, such cables and conduits are not shown in FIG. 11A, but it should be understood that they are present nonetheless.

[0203] 11A also includes a wafer support Z actuator 1146 that can provide movable support to the wafer support column 1144. The wafer support Z actuator 1146 can be actuated to move the wafer support column 1144, and the wafer support 1124 supported thereby, vertically up and down, for example, by up to several inches, within the reaction volume 1120 of the process chamber 1102. In doing so, the gap distance X between the substrate 1122 and the underside of the showerhead 1110 can be adjusted in response to various process conditions.

[0204] The wafer support 1124 may also, in some embodiments, include one or more edge rings that can be used to control and / or fine-tune various process conditions. In FIG. 11A , an upper edge ring 1138 is provided, for example, above lower edge rings 1140a and 1140b, which are supported by a wafer support housing 1142 and a third lower edge ring 1140c. The upper edge ring 1138 may, for example, be generally subjected to the same processing environment as the substrate 1122, while the lower edge rings 1140a / b / c may generally be shielded from the processing environment. Due to the increased exposure of the upper edge ring 1138, the upper edge ring 1138 may have a limited lifespan and require more frequent replacement or cleaning compared to the lower edge rings 1140a / b / c.

[0205] The apparatus 1100 may also include a system for removing process gases from the process chamber 1102 during and after processing. For example, the process chamber 1102 may include an annular plenum 1156 surrounding the wafer support posts 1144. The annular plenum 1156 may then be fluidly connected to a vacuum foreline 1152, which may be connected to a vacuum pump, such as one that may be located below the subfloor below the apparatus 1100. A control valve 1154 may be provided between the vacuum foreline 1152 and the process chamber 1102 and may be actuated to control flow into the vacuum foreline 1152. In some embodiments, a baffle 1150, e.g., an annular plate or other structure, may be provided that may function to distribute flow into the annular plenum 1156 more evenly around the circumference of the wafer support posts 1144, thereby reducing the likelihood of flow non-uniformities in the reactants flowing across the substrate 1122.

[0206] The showerhead 1110 is shown as a dual-plenum showerhead 1110, including a first plenum 1112 supplied with process gas via a first inlet 1116 and a second plenum 1114 supplied with process gas via a second inlet 1118. Generally, two plenums can be used to maintain separation between the precursors and the reverse reactant prior to release. The showerhead 1110 may have three or more plenums in some embodiments. In some cases, a single plenum is used to deliver precursors to the reaction space 1120 of the processing chamber 1102. Each plenum can have a corresponding set of gas distribution ports that fluidly connect the respective plenum with the reaction space 1120 through the faceplate of the showerhead 1110 (the faceplate is the portion of the showerhead 1110 interposed between the lowermost plenum and the reaction space 1120).

[0207] The first inlet 1116 and the second inlet 1118 of the showerhead 1110 may be supplied with process gases via a gas supply system, which may be configured to supply one or more precursors and / or counter-reactants as described herein. The illustrated apparatus 1100 is configured to supply multiple precursors and multiple counter-reactants. For example, a first valve manifold 1168a may be configured to supply a precursor to the first inlet 1116, and a second valve manifold 1168b may be configured to supply another precursor or another counter-reactant to the second inlet 1118.

[0208] A first valve manifold 1168a can be configured to supply one or more precursors to the first inlet 1116, and a second valve manifold 1168b can be configured to supply other precursors or other reactants to the second inlet 1118. In this example, the first valve manifold 1168a includes, for example, multiple valves A1-A5. Valve A2 can be, for example, a three-way valve having one port fluidly connected to a first vaporizer 1172a, another port fluidly connected to a bypass line 1170a, and a third port fluidly connected to a port on another three-way valve A3. Similarly, valve A4 can be another three-way valve having one port fluidly connected to a second vaporizer 1172b, another port fluidly connected to a bypass line 1170a, and a third port fluidly connected to a port on another three-way valve A5. One of the other ports on valve A5 can be fluidly connected to the first inlet 1116, and the remaining port on valve A5 can be fluidly connected to one of the remaining ports on valve A3. The remaining port on valve A3 can then be fluidly connected to valve A1, which can be fluidly interposed between valve A3 and a purge gas source 1174, e.g., nitrogen, argon, or other suitable inert gas (for the precursor and / or back reactant). In some embodiments, only the first valve manifold is used.

[0209] For purposes of this disclosure, the term "fluidically connected" is used in reference to volumes, plenums, holes, etc. that may be connected to each other to form a fluid connection, similar to how the term "electrically connected" is used in reference to components that are connected to each other to form an electrical connection. The term "fluidically interposed," when used, can refer to a component, volume, plenum, or hole that is fluidly connected to at least two other components, volumes, plenums, or holes, such that fluid flowing from one of those other components, volumes, plenums, or holes to the other of those components, volumes, plenums, or holes will first flow through the "fluidically interposed" component before reaching the other component, volume, plenum, or hole. For example, if a pump is fluidly interposed between a reservoir and an outlet, fluid flowing from the reservoir to the outlet will first flow through the pump before reaching the outlet.

[0210] The first valve manifold 1168a may be controllable to, for example, flow vapor from one or both of the vaporizers 1172a and 1172b into the process chamber 1102 or through the first bypass line 1170a to the vacuum foreline 1152. The first valve manifold 1168a may also be controllable to flow purge gas from a purge gas source 1174 to the first inlet 1116.

[0211] For example, to flow vapor from the first vaporizer 1172a to the reaction space 1120, valve A2 can be actuated to first flow the vapor from the first vaporizer 1172a through the first bypass line 1170a. This flow can be maintained for a period of time sufficient to allow the vapor flow to reach a steady-state flow condition. After a sufficient amount of time has passed (or after a flow meter, if used, indicates that the flow rate is stable), valves A2, A3, and A5 can be actuated to direct the vapor flow from the first vaporizer 1172a to the first inlet. Similar operations using valves A4 and A5 can be performed to deliver vapor from the second vaporizer 1172b to the first inlet 1116. In some cases, it may be desirable to purge one of the vapors from the first plenum 1112 by actuating valves A1, A3, and A5 to allow purge gas from the purge gas source 1174 to flow into the first inlet 1116. In some additional embodiments, it may be desirable to simultaneously flow vapor from one of vaporizers 1172a or 1172b in parallel with flowing gas from the purge gas into first inlet 1116. Such an embodiment can be used to dilute the concentration of reactants contained in such vapor.

[0212] It will be appreciated that the second valve manifold 1168b can be controlled in a similar manner, for example, by controlling valves B1-B5, to supply vapor from vaporizers 1172c and 1172d to the second inlet 1118 or to the second bypass line 1170b. Additionally, it will be appreciated that different manifold arrangements can be utilized as well, including a single integrated manifold that includes valves to control the flow of precursors, back reactants, or other reactants to the first inlet 1116 and the second inlet 1118.

[0213] As previously mentioned, some devices 1100 may feature fewer vapor sources, e.g., only two vaporizers 1172, in which case valve manifold 1168 may be modified to have fewer valves, e.g., only valves A1-A3.

[0214] As described above, an apparatus such as the apparatus 1100 that can be used to perform dry deposition of a film can be configured to maintain a specific temperature profile within the process chamber 1102. In particular, such an apparatus 1100 can be configured to maintain the substrate 1122 at a lower temperature, e.g., at least 25° C. to 50° C. lower, than most of the equipment of the apparatus 1100 that directly contacts the precursors and / or reverse reactants. In addition, the temperature of the equipment of the apparatus 1100 that directly contacts the precursors and / or reverse reactants can be maintained at a high enough temperature level to prevent condensation of vaporized reactants on the surfaces of such equipment. At the same time, the temperature of the substrate 1122 can be controlled to a level that promotes condensation, or at least deposition, of the reactants on the substrate 1122.

[0215] To provide such temperature control, various heating systems can be included in the apparatus 1100. For example, the process chamber 1102 can have a receptacle for receiving a cartridge heater 1158; for example, in the case of a process chamber 1102 having a generally cylindrical interior volume but a square or rectangular exterior, vertical holes can be drilled in the four corners of the chamber 1102 housing to receive the cartridge heater 1158. In some embodiments, the showerhead 1110 can be covered with a heater blanket 1160, which can be used to apply heat to the entire exposed top surface of the showerhead 1110 and maintain an elevated showerhead temperature. It can also be beneficial to heat the various gas lines used to direct vaporized reactants from the vaporizer 1172 to the showerhead 1110. For example, resistive heater tape can be wrapped around such gas lines and used to heat the gas lines to a high temperature. 11A, all gas lines through which precursors and / or counter reactants may flow are shown as heated, including bypass line 1170. The only exceptions are the gas lines from valve manifold 1168 to first inlet 1116 and second inlet 1118, which are very short and can be indirectly heated by showerhead 1110. Of course, these gas lines can also be actively heated, if desired. In some embodiments, heat can also be supplied to gate valve 1106 by providing a heater in close proximity to the gate valve.

[0216] The various operating systems of the apparatus 1100 can be controlled by a controller 1184, which may include one or more processors 1186 and one or more memory devices 1188 operably connected to each other and communicatively connected to the various systems and subsystems of the apparatus 1100 to provide control functions for these systems. For example, the controller 1184 may be configured to control valves A1-A5 and B1-B5, the various heaters 1158, 1160, the vaporizer 1172, the regulator valve 1154, the gate valve 1106, the wafer support Z actuator, etc.

[0217] Another feature that the apparatus 1100 may include is shown in FIG. 11B, which illustrates an enlarged cross-sectional side view and plan view of a portion of the substrate 1122, top plate 1128, and upper edge ring 1138 of FIG. 11A. As can be seen, in some implementations, the substrate 1122 may be elevated from the majority of the top plate 1128 by a plurality of small mesas 1176, which may be shallow bosses that protrude a small distance from the nominal upper surface of the top plate 1128 to provide a backside gap 1178 between the underside of the substrate 1122 and the majority of the top plate 1128. A peripheral wall feature 1177 may be provided on the periphery of the top plate 1128. The peripheral wall feature 1177 may extend around the entire periphery of the top plate 1128 and may be nominally the same height as the mesas 1176. During processing operations, a generally inert gas, such as helium, can flow into the backside gap 1178 through one or more gas ports 1182. The gas can then flow radially outward before encountering the peripheral wall feature 1177, which then restricts such radially outward flow and traps a high-pressure region of gas between the substrate 1122 and the top plate 1128. Any inert gas that leaks beyond the peripheral wall 1177 can eventually escape through the radial gap 1180 between the outer edge of the substrate 1122 and a portion of the upper edge ring 1138. Such gas can act to prevent gases emitted by the showerhead 1110 from reaching the underside of the substrate 1122, thereby protecting the underside of the substrate from undesirable effects of the processing operations being performed. At the same time, the gas emitted in the region of the backside gap 1178 can also act to increase thermal coupling between the substrate 1122 and the top plate 1128, thereby allowing the top plate 1128 to more effectively heat or cool the substrate 1122. Due to the high pressure provided by the peripheral wall, the gas in the area of ​​the back gap 1178 may also be denser than the gas in the rest of the chamber, thus providing more effective thermal coupling between the substrate 1122 and the top plate 1128.

[0218] Controller 1184 can be configured, for example, through the execution of computer-executable instructions, to cause device 1100 to perform various operations consistent with the above disclosure.

[0219] Once the metal-containing resist film is deposited on the substrate 1122, the substrate 1122 may be transferred to one or more subsequent process chambers or tools for additional operations (e.g., any described herein), as described above. Additional deposition apparatus are described in International Patent Application No. PCT / US2020 / 038968, filed June 22, 2020, and entitled "APPARATUS FOR PHOTORESIST DRY DEPOSITION," which is incorporated herein by reference in its entirety.

[0220] conclusion A process and apparatus for dry development of metal and / or metal oxide photoresists to form patterning masks, for example in EUV patterning scenarios, is disclosed.

[0221] It will be understood that the examples and embodiments described herein are for illustrative purposes only, and that various modifications or changes will be suggested to those skilled in the art in light thereof. Various details have been omitted for clarity, but various design alternatives can be implemented. Accordingly, the examples are to be considered illustrative rather than restrictive, and the disclosure is not to be limited to the details given herein, but can be modified within the scope of the disclosure.

Claims

1. 1. A method of developing a resist, comprising the steps of: Providing a photopatterned metal-containing resist on a surface of a semiconductor substrate in a process chamber; dry developing the photo-patterned metal-containing resist by selectively removing portions of the photo-patterned metal-containing resist by exposure to a developing chemistry that includes an organic vapor to form a resist mask; Including, The method of claim 1, wherein the organic vapor comprises a carboxylic acid.

2. A method according to claim 1, comprising: The method of claim 1, wherein the organic vapor comprises trifluoroacetic acid.

3. 1. A method of developing a resist, comprising the steps of: Providing a photopatterned metal-containing resist on a surface of a semiconductor substrate in a process chamber; dry developing the photo-patterned metal-containing resist by selectively removing portions of the photo-patterned metal-containing resist by exposure to a developing chemistry that includes an organic vapor to form a resist mask; Including, The method, wherein the organic vapor comprises trifluoroacetic anhydride, acetic anhydride, trichloroacetic acid, monofluoroacetic acid, difluoroacetic acid, chlorodifluoroacetic acid, thioacetic acid, or thioglycolic acid.

4. 1. A method of developing a resist, comprising the steps of: Providing a photopatterned metal-containing resist on a surface of a semiconductor substrate in a process chamber; dry developing the photo-patterned metal-containing resist by selectively removing portions of the photo-patterned metal-containing resist by exposure to a developing chemistry that includes an organic vapor to form a resist mask; Including, The method of claim 1, wherein the organic vapor comprises hexafluoroacetylacetone.

5. 1. A method of developing a resist, comprising the steps of: Providing a photopatterned metal-containing resist on a surface of a semiconductor substrate in a process chamber; dry developing the photo-patterned metal-containing resist by selectively removing portions of the photo-patterned metal-containing resist by exposure to a developing chemistry that includes an organic vapor to form a resist mask; Including, The method wherein said developing chemistry comprises a vapor phase mixture of a halogenated carboxylic acid and a hydrogen halide.

6. 6. The method according to any one of claims 1 and 2 to 5, The method, wherein dry developing the photo-patterned metal-containing resist comprises reacting the organic vapor with the photo-patterned metal-containing resist to form a volatile compound at a temperature less than about 200° C.

7. 6. The method according to any one of claims 1 and 2 to 5, The method, wherein dry developing the photopatterned metal-containing resist comprises exposing to at least the organic vapor in a plasma-free thermal process.

8. 6. The method according to any one of claims 1 and 2 to 5, The method, wherein the photopatterned metal-containing resist is a photopatterned metal-containing EUV resist, and the photopatterned metal-containing EUV resist is an organometallic oxide or organometallic containing film.

9. 6. The method according to any one of claims 1 and 2 to 5, dry developing the photo-patterned metal-containing resist includes selectively removing EUV non-exposed portions of the photo-patterned metal-containing resist relative to EUV exposed portions using the developing chemistry to form the resist mask.

10. 1. A method for removing residue from a process chamber, comprising: depositing a metal-containing resist material on a surface of a semiconductor substrate in a process chamber, a portion of the metal-containing resist material forming a residue on one or more surfaces of the process chamber; introducing a dry etchant comprising an organic vapor into the process chamber, the dry etchant at least partially removing the residue on the one or more surfaces of the process chamber; A method comprising:

11. 11. The method of claim 10, The method of claim 1, wherein the organic vapor comprises a carboxylic acid.

12. 12. The method of claim 11, The method of claim 1, wherein the organic vapor comprises trifluoroacetic acid.

13. 11. The method of claim 10, The method, wherein the organic vapor comprises trifluoroacetic anhydride, acetic anhydride, trichloroacetic acid, monofluoroacetic acid, difluoroacetic acid, chlorodifluoroacetic acid, thioacetic acid, or thioglycolic acid.

14. 11. The method of claim 10, The method of claim 1, wherein the organic vapor comprises hexafluoroacetylacetone.

15. 15. The method according to any one of claims 10 to 14, The method, wherein the dry etchant comprises a vapor phase mixture of a halogenated carboxylic acid and a hydrogen halide.

16. 15. The method according to any one of claims 10 to 14, The method, wherein at least partially removing the residue comprises reacting the organic vapor with the metal-containing resist material to form a volatile compound at a temperature less than about 200°C.

17. 15. The method according to any one of claims 10 to 14, The method, wherein at least partial removal of the residue comprises exposing to at least the organic vapor in a plasma-free thermal process.

18. 15. The method according to any one of claims 10 to 14, The method, wherein the metal-containing resist material is an organometallic oxide or an organometallic-containing film.

19. 15. The method according to any one of claims 10 to 14, purging the process chamber after introducing the dry etchant to remove residual dry etchant from the process chamber; conditioning the one or more surfaces of the process chamber by forming a protective coating of the metal-containing resist material on the one or more surfaces of the process chamber; The method further comprising:

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